Proceeding ACSAC ISBN PDF

The 7
th
ASIAN CROP SCIENCE ASSOCIATION CONFERENCE
Improving food, energy and environment with better crops
Proceedings of The 7
th
ACSA Conference 2011 i
ISBN: 978-602-17500-0-1

PROCEEDINGS

The 7
th
Improving food, energy, and environment with better crops

IPB International Convention Center
Bogor, Indonesia, 27-30 September 2011

Research Center for Bioresources and Biotechnology
Bogor Agricultural University
2013
ii Proceedings of The 7
th
ACSA Conference 2011

Copyright:
This proceedings published by Research Center for Bioresources and Biotechnology,
(Pusat Penelitian Sumberdaya Hayati dan Bioteknologi, Institut Pertanian Bogor)
Jln. Kamper, Gedung PAU Kampus IPB Darmaga, Bogor (16680), Indonesia.

th
ACSA Conference 2011 iii
ISBN: 978-602-17500-0-1

PROCEEDINGS

The 7
th
Improving food, energy, and environment with better crops

IPB International Convention Center
Bogor, Indonesia, 27-30 September 2011

Editors
Chief:
Suharsono
(Research Center for Bioresources and Biotechnology, Bogor Agricultural University)

Members:
Hiroshi Ehara
(Graduate School of Bioresources, Mie University, Japan)
Hayati Minarsih
(Indonesian Biotechnology Research of Estate Crops)
Komang G Wiryawan
(Faculty of Animal Sciences, Bogor Agricultural University)
Miftahuddin
(Faculty of Mathematics and Natural Sciences, Bogor Agricultural University)
Muhamad Yunus
(Indonesian Agency for Agricultural Research and Development, Ministry of Agriculture)
Tri Muji Ermayanti
(Research Center for Biotechnology, Indonesian Institute of Sciences)
Utut Widyastuti

Technical Editor:
Noor F Mardatin

Bogor, January 2013
iv Proceedings of The 7
th
th
ACSA Conference 2011 v

Foreword from the Chairman of Organizing Committee

We are currently facing an increasing population, diminishing resources and also escalating
environmental problems. These inconvenient conditions could be solved by intensifying our
attention to develop efficient, stable, and sustainable crop production systems. To achieve this goal,
the cooperation of crop scientists working on different aspects from basic to applied sciences, and
different commodities from food crops as considered the basic need of human being to ornamental
crops considered as secondary need, transcending the boundaries of region and nations is
necessary.
With the intention to accommodate the communication among researchers on crop science,
the Asian Crop Science Association (ACSA) conducts regular international conference every three
years. During four days on September 27-30th, 2011, we had successfully organized the 7
th

Conference of ACSA with the theme on Improving Food, Energy, and Environment with Better
Crops, in Bogor, Indonesia. This event had been attended by 240 participants coming from 17
different countries. During three days of the conference, 13 papers were presented by invited
speakers in the plenary sessions, 81 papers were in the parallel sessions, and 71 posters were
presented in the poster sessions. This conference was in conjunction to the 48th anniversary of
Bogor Agricultural University, annual meeting of Crop Science Society of Japan (CSSJ), Japanese
Society of Breeding (JSB) and Japanese Society of Tropical Agriculture (JSTA), and the kick off
meeting and workshop of Japan International Research Center for Agricultural Science (JIRCAS).
The scientific activities were composed of three seminars: (1) ACSA Conference with the
theme on Improving food, energy, and environment with better crops, (2) seminar of annual
meeting of CSSJ, JSB and JSTA with the theme on Improvement of crop performance for
sustainable agricultural development in wetlands, and (3) workshop of JIRCAS with the theme on
"Rice innovation for environmentally sustainable production systems.
On behalf of the editor and also the organizing committee, I would like to express our
happiness that the scientific papers presented in the Conference can be finally compiled and
published in the form of Proceedings of the 7
th
Asian Crop Science Association Conference.
We apologize for the delay to publish these proceedings. We sincerely hope that these
Proceedings will be useful and beneficial for all parties.

Chairman of OC and Chief Editors,

Prof. Dr. SONY SUHARSONO

vi Proceedings of The 7
th

Foreword from the Rector of Bogor Agricultural University

I would like to express my happiness that The Proceedings of The 7
th
Conference of Asian
Crop Science Association (ACSA) can finally be published. Looking on the number of scientific
papers coming from different countries and aspects, it is certainly that many tasks had been done to
publish these proceedings. My expression of appreciation and gratitude are addressed to the
editors who had been working very hard to finish the proceedings.
Crop is very important to human and there is no life without crop. From crop we obtain food
and feed. With the increasing of the world population, the requirement for crop is increasing
substantially, therefore, serious efforts must be undertaken to improve crop production to supply
sufficient food for human. In addition, the climate change forces us to adapt to this environmental
changes. From this point of view, the development of crop science is highly important, from basic to
applied sciences, and collaboration amongst scientists is necessary to accelerate the progress of
crop development. Crop does not only provide food, but also provides a future energy sources
which is more friendly to the environment, therefore, the proceedings consisted of the scientific
papers of the 7
th
Conference of ACSA with the theme of Improving food, energy, and environment
with better crops is highly relevant to the current situation.
ACSA is expected to play major role in crop science development and in coordinating the
collaboration amongst scientists, not only in Asia but also throughout the world. Therefore I
personally and as a Rector of Bogor Agricultural University strongly support ACSA as a medium for
collaboration to share knowledge and experiences in recent advances of crop science development.
Finally, I extend my gratitude to contributors, and sponsors for participating in the compiling
all scientific papers in the proceedings. I believe that these proceedings will enrich our knowledge,
especially in crop sciences, and beneficial to mankind.

Rector of Bogor Agricultural University,

Prof. HERRY SUHARDIYANTO, PhD.
th
ACSA Conference 2011 vii

KEYNOTE ADDRESS
MINISTER OF AGRICULTURE REPUBLIC OF INDONESIA
AT THE OPENING CEREMONY OF THE 7
th
ACSA CONFERENCE
Bogor, 27-30 September 2011

Distinguished guests,
Rector of Bogor Agricultural University,
Chairman of Asian Crop Science Association (ACSA),
Chairman of Crop Science Society of Japan,
Director of Japan International Research Center for Agricultural Sciences (JIRCAS),
Ladies and Gentlemen,

Assalamu'alaikum warahmatullaahi wabarakaatuh,

It is a great pleasure for me to be here with you and warmly welcome you all in this
important gathering of The 7
th
ACSA conference. On behalf of the Government of the Republic of
Indonesia, it is also a great honor and privilege for me to extend our warm welcome to all
participants.
It is a great pleasure also for me to congratulate for 48
th
anniversary of IPB and warm
welcome and success for kick off meeting of Crop Science Society and Japan International
Research Center for Agricultural Sciences (JIRCAS).

The on going changes in the economy, resources competition from other sectors,
environmental changes, increasing commercialization of agricultural activities, and the importance
of international trade mean that the way of agricultural product will be produced in the future will be
substantially different.
Some traditional agriculture-growing areas may lose their comparative advantage while
others may become new growth centers for agriculture product. Clearly, there is a need to develop
a new vision for future agriculture activities given these global trends and likely scenarios. This
vision is needed to strategically position investment in agricultural research, technology delivery,
and the design of policy reforms.
Agriculture in the next future will not only need to produce enough food and energy for
population, but will also be the key to conserve environment for a sustainable food production.
FAOs latest forecast for world cereal production in 2011 stands at 2,302 million tonnes, 2.9 percent
up from the 2010 harvest. World cereal utilization in 2011/12 is forecast to increase by 1.2 percent
from 2010/11. Given the latest production forecast and the expectation for utilization in 2011/12,
MINISTRY OF AGRICULTURE
REPUBLIC OF INDONESIA

viii Proceedings of The 7
th
world cereal stocks at the close of crop season ending in 2012 are now estimated at about 486
million tonnes.
Except for rice, the inventories of which are forecast to increase, stocks of coarse grains
and wheat anticipated to decline. With total cereal production in 2011 below the anticipated
utilization, international price are likely to remain high, especially in the wheat and coarse grain
market. In Asian countries, high food prices and the generally good rainfall situation have been
conducive to bumper food production. In the 2011, annual harvest for rice are expected to increase
in China, India, Vietnam, Indonesia, Thailand and Philippines.
Up to 2050 the worlds population will rise from 6 bn to 8 bn (33%) and about 50% of the
total population are lives in Asia. Simultaneously, demand of food will increase by 50%, demand of
water will increase 30%, and demand for energy will increase by 50%.
Considering those features, the approach need for adaptation are (1) public awareness to
enhance participation, (2) improving institutional capacity building, (3) policy reform, (4) strong
enhancing research and study.

In terms of energy, more than 40% of our populations engage in producing energy from
fossil fuel and wood to run their daily activities including agriculture. So there is a need for using a
sustainable source of fuel in the rural area in the future.
The Central Bureau of Statistics (BPS) reported that population growth in Indonesia during
the period of 2000 to 2010 was 1.49 percent per year, compared to 1.45 percent during the period
of 1990 to 2000. The 0.04 percent increase for the current population (237 million people) resulted
in a very big increase in food demand. If we do not make a serious effort to control birth rate, the
country's population may reach an alarming 400 million in the year 2060. In the case of rice, with
consumption rate of 134 kg/cap/year, the demand for hulled rice in 2015 will be 44,4 million tons. In
addition to the pressure on the demand, large population also represent a serious threat to
environment that cause unsanitary living conditions, the depletion of resources, environmental
pollution, and poverty, which are the root of environmental problems.
The second problem is diminishing natural resources, particularly land and water
resources. Irrigation water is an important production factor in rice production systems but it is no
longer available in unlimited quantities in rice-growing areas due the increase of competition from
domestic use. Meanwhile, conversion of rice field to non-agriculture use is estimated about 100.000
ha annually. These two will significantly limit food production capacity in the country.
The third problem is the impact of global warming. Indonesia is already a significant emitter
of greenhouse gases due to deforestation and land-use change, estimated at 2 million hectares per
year and accounts for 85 percent of the countrys annual greenhouse gas emissions. The effects
will be felt more acutely by the poorest people, who are living in the most marginal areas that are
vulnerable to drought, floods and landslides. International Food Policy Institute estimates that rice
production in developing countries, will be reduced as much as fifteen percent (15%), and the price
of rice will increase to twelve percent (12%) in 2050.

Opportunities to cope with fore mentioned problems are by using environmentally friendly
technologies. Luckily, our researchers have generated innovative technology for better crops that
increase productivity with environmentally friendly manners. Among of them are more aerobic
cultural practices, include intermittent irrigation and aerobic rice varieties, specific site nutrient
management, integrated pest management, and higher yield rice varieties.

th
ACSA Conference 2011 ix
I believe that through the 7
th
Asian Crop Science Association Conference, we are all will
share knowledge and experience; therefore, I hope this conference will come up with
recommendation to cope all those problems.
Finally, with Bismillahirrahmanirrohim, I declare The 7
th
ACSA Conference officially
open. Have a pleasant meeting and please enjoy your stay in Indonesia, especially in Bogor.

Wassalaamualaikum warahmatullaahi wabarakaatuh.

Minister of Agriculture,

SUSWONO

x Proceedings of The 7
th
th
ACSA Conference 2011 xi
Table of Content

page

Foreword from the Chairman of Organizing Committee . v
Foreword from the Rector of Bogor Agricultural University ....................................................... vi
Keynote Address . vii
Table of Content . xi

Invited speakers:

1. Improving Photosynthesis to Increase the Productivity of Crops (Abstract)
(Akiho Yokota)

1

2. Impacts of Climate Change and Climate Variability on Productivity of Food Grain
Crops (Abstract)
(PV Vara Prasad) ...

2

3. The Plant Improvement of Tolerance to Oxidative Stresses (Abstract)
(Shigeru Shigeoka) ..

3

4. Salt Resistance Mechanism of Metroxylon sagu, Starch-producing Palm
(Hiroshi Ehara, Wikanya Prathumyot, Hitoshi Naito) ..

5

5. How to Increase Food Crop Productivity in Asia (Abstract)
(Narasimham Upadyayula) .

11

6. Biosynthesis of Nicotine as an Anti-insect Defense in Plants (Abstract)
(Takashi Hashimoto)

12

7. Food Security and Agriculture Biotechnology Progress in Indonesia (Abstract)
(Tantono Subagyo, Fadlilla Dewi Rakhmawaty) ..

13

8. 14-3-3 Proteins Act as Intracellular Receptors for Rice Hd3a Florigen (Abstract)
(Hiroyuki Tsuji, Ken-ichiro Taoka, Izuru Ohki, Kyoko Furuita, Kokoro Hayashi,
Tomoko Yanase, Midori Yamaguchi, Chika Nakashima, Yekti Asih Purwestri, Shojiro
Tamaki, Yuka Ogaki, Chihiro Shimada, Atsushi Nakagawa, Chojiro Kojima, Ko
Shimamoto) ......

14

9. Food Security and Sustainable Agriculture (Abstract)
(Paul PS Teng)

15

10. Improvement of Oil Palm Productivity (Abstract)
(Tony Liwang) ....

17

xii Proceedings of The 7
th

Concurrent Session and Poster Presentations:
Rice
1. Characterization of Water Availability, Management Practices and Grain Yield for
Deepwater Rice in Northwest Cambodia
(Nguyen T.B. Yen, Akihiko Kamoshita, Yuji Araki, Makara Ouk) .

19

2. Submergence Escape in Oryza glaberrima Steud.
(J un-Ichi Sakagami, Chiharu Sone, Naoyoshi Kawano)

24

3. Toposequnential Variation in Soil Fertility and Limiting Nutrient for Rice Growth in
the White Volta Floodplain of Northern Ghana
(Yasuhiro Tsujimoto, Yukiyo Yamamoto, Keiichi Hayashi, Alhassan I Zakaria,
Yahaya Inusah, Tamao Hatta, Mathias Fosu, Jun-Ichi Sakagami)

29

4. Varietal Differences of Rice (Oryza sativa L.) Genotypes for Aleurone Traits
Contributing to Lipid Content
(Ohn Mar Khin, Masao Sato, Tong Li-Tao, Yuji Matsue, Atsushi Yoshimura,
Toshihiro Mochizuki) ...

34

5. Development of New Cytoplasmic Male Sterile Lines with Good Flowering
Behavior for Hybrid Rice Breeding
(Indrastuti A Rumanti, Bambang S Purwoko, Iswari S Dewi, H Aswidinnoor)

39

6. Genetic Analysis of Superior Double Haploid Rice Lines Developed from Anther
Culture
(Muhammad Syafii, Bambang S Purwoko, Iswari S Dewi) .

45

7. QTLs on Chromosome 12 Responsible for Expressing Root Plasticity under
Transient Soil Moisture Fluctuation Stress in Rice
(J onathan M Niones, Yoshiaki Inukai, Akira Yamauchi)

51

8. Yield and Related Traits in Two Japonica Rice Lines Carrying Ur1 Gene
(Stanis Malangen, Takumi Iwakura, Toru Hata, Takeshi Akaoka, Amol Dahal,
Masayuki Murai) .....................................................................................

56

9. Oxidative Stress and its Relation to Radiation Use Efficiency in Rice Growing
under Rainfed Condition in Northeast Thailand
(Kohtaro Iseki, Koki Homma, Boonrat Jongdee) ....................................................

61

10. The Growth Characteristics of Some Varieties of Acehs Local Rice (Oriza sativa
L.) on Acid Soils
(Elly Kesumawati, Erita Hayati, Muhafaz Zulusfitri) ................................................

66

11. Effect of NPK Fertilizer and Biochar Applications on Growth and Yield of Irrigation
Rice
(Zaitun, Khairun Nisa, Sufardi, Chairunas, Anischan Gani, Peter Slavich, Malem
McLeod) ....................................................................................................................

72

th
ACSA Conference 2011 xiii

12. Effects of New Foliar-Application Fertilizer Containing 5-Aminolevlinic Acid on
Yield Increase of Direct-Sowing Rice Plants
(Ryuji Yoshida, Keitaro Watanabe) .........................................................................

76

13. Yield Stability Evaluation of Upland Rice Lines Obtained from Anther Culture
(Deni D Sulaeman, Bambang S Purwoko, Iswari S Dewi, Muhamad Syukur,
Desta Wirnas, Heni Safitri) .......................................................................................

80

14. Yield and Blast Resistance Evaluation of Upland Rice Lines with New Plant Type
Characters
(J ose MA Ornai , Bambang S Purwoko, Desta Wirnas, Iswari S Dewi, Heni
Safitri) .......................................................................................................................

85

15. Functional Analysis of Drought-Induced OsLEA3 Promoter Isolated from Batutegi
Rice Cultivar
(Agus Rachmat, Satya Nugroho, Bernadetta Rina Hastilestari, Kinasih Prayuni,
Sudarsono) ...

91

16. Evaluation of the Nutritional Environment for Rice in Cianjur, Indonesia, for
Development of an Advanced Basin Model for Asia
(Koki Homma, Gunardi Sigit, Handarto, Masayasu Maki, Chiharu Hongo, Koshi
Yoshida, Kazuo Oki, Hiroaki Shirakawa, Tatsuhiko Shiraiwa, Ritsuko Hara, Mitsuo
Kambayashi, Yoshihiro Hirooka, Hiroki Iwamoto) ..

96

17 The Nutritional Environment in Nonfertilized Rice Production and Its Effect on the
Nutritional Quality of Brown Rice
(Ritsuko Hara, Koki Homma, Yoshihiro Hirooka, Mitsuo Kuwada, Tatsuhiko
Shiraiwa) ...

101
18 Effect of Slow Release Fertilizer on Yield and Yield Components in Chinese High-
Yielding Rice Cultivars
(Toshiaki Kokubo, Akira Miyazaki, Tetsushi Yoshida, Yoshinori Yamamoto, Jing
Ju, Yulong Wang) ....

107
19 Drought Resistance of NERICA Compared with Asian Rice, African Rice and
Millets in the Field with Different Fertilization Levels
(Michihiko Fujii, Seiji Ishihara, Ryohta Shinohara) ..

113
20 Social Experiment of Volumetric Irrigation Fee Scheme: Case of Gravity Irrigation
System in Bohol, the Philippines
(Shigeki Yokoyama, Kei Kajisa, Tatsuro Miyazaki) .

119
21 Ultraviolet-induced Fluorescence of Rice Leaf as Influenced by Nitrogen
Application and Cultivars
(Mikio Sekinuma, Takehiro Natori, Futoshi Sasaki, Futoshi Kato, Naoto Inoue)

125
22 Locus for Malate Secretion in Rice Chromosome 3
(Miftahudin, Irfan Martiansyah, Dewi Indriyani Roslim, Tatik Chikmawati) ............

130

xiv Proceedings of The 7
th
Maize
1. Responses of Nutrient Efficient Maize Genotypes to Bio-fertilizer at Low Chemical
Fertilizer Doses
(Marlin Sefrila, Munandar, Renih Hayati, Sabaruddin) .

137

Cassava
1. Kinetin and Calcium Pantothenate Effects on Shoot Multiplication in In Vitro
Cultured Cassava Var. Adira 2 and Adira 4
(Nurul Khumaida, Sintho Wahyuning Ardie, Candra Catur Nugroho, Suwarto) .....

141
Wheat
1. Wet Injury of Wheat in Upland Field Converted from Paddy Field in Japan
(Kentaro Kawaguchi) ..............................................................................................

147

2. Roles of Root System Development and Function in the Growth and Yield under
Waterlogged Condition in Common Wheat
(Tomohito Hayashi, Tomofumi Yoshida, Kiyoshi Fujii, Takako Tsuji, Yurie Okada,
Eriko Hayashi, Akira Yamauchi) ...............................................................................

153

Sago
1. Growth and Physiological Responses of Sago Palm Against Aluminum Stress in
Acidic Conditions
(Ornprapa Anugoolprasert, Hiroshi Ehara, Shina kinoshita, Hitoshi Naito,
Somchai Chakhatrakan) ...........................................................................................

159
2. Transplanted Sucker Stem Growth in Sago Palm (Metroxylon sagu Rottb.) before
Trunk Formation
(Satoshi Nakamura, Keita Nabeya, Mutsumi Akama, Teiji Nakamura, Youji Nitta,
Manabu Watanabe, Yusuke Goto) ...........................................................................

165
Soybean
1. Secondary Aerenchyma Formation and Root Growth Response of Soybean
(Glycine max) Seedlings under Flooded Conditions
(Toshihiro Mochizuki, Satomi Sakazono, Sayuri Kajihara, Satoshi Shimamura) ..

169
2. Agronomical Performances of Soybean Cultivated under Saturated Soil Culture
on Tidal Swamps
(M Ghulamahdi, M Melati, S A Aziz, A Junaedi, Sahuri, Y Puspitasari, D Sagala) .

175
3. Agronomic Performance of F7 Large Seed Soybean Breeding Lines in Medium
Plains
(Darman M Arsyad, Asadi) ......................................................................................

180
4. Organically Production of Soybean Supported by Fertilizers Residue under
Saturated Soil Culture
(Maya Melati, Kalimatul Jumro) ...............................................................................

185
5. Factors Causing the Soybean Yield Gaps between Japan and USA
(Keisuke Katsura, Koki Homma, Yohei Kawasaki, Larry C Purcell, Randall L
Nelson, Taiki Yoshihira, Tatsuhiko Shiraiwa)

191
th
ACSA Conference 2011 xv
6. Photosynthetic Acclimation to Elevated CO
2
in Soybean
(Mochamad Arief Soleh, Hai Yan, Tomohiro Konno, Makie Kokubun, Ryoji
Sameshima) .

196
7. The Effect of Organic Materials and Decomposer on Soybean Growth and
Production
(Sandra Arifin Aziz, Sri Ayu Dwi Lestari) ................................................................

200
8. Yield and Dry Matter Production of Japanese and US Soybean Cultivars under
Drought Stress
(Yohei Kawasaki, Yu Tanaka, Keisuke Katsura, Tatsuhiko Shiraiwa) ....................

205
9. Selection of F4, F5 and F6 Soybean Breeding Lines for High Yield and Large
Sees Size
(Darman M Arsyad, Asadi) ..

209
10. Effect of Hydrogen Peroxide Spraying on Drought Stress in Soybean Plant
(Yushi Ishibashi, Haruka Yamaguchi, Takashi Yuasa, Mari Iwaya-Inoue, Susumu
Arima, Shao-Hui Zheng) .

215
11. Productivity of Several Lines of Soybean in Majalengka, West Java, Indonesia
(Alia Astuti, Ence Darmo Jaya Supena, Suharsono) .

220
Beans
1. Paclobutrazol Application Effectiveness on Growth of Two Peanut (Arachis
hypogaea L.) Varieties
(Iskandar Lubis, Aries Kusumawati, Munif Ghulamahdi, Heni Purnamawati,
Yudiwanti WE Kusumo, Ahmad Ghozi Mansyuri, Sri Astuti Rais) ............................

225
2. Effect of Source or Sink Restriction on Flowering, Podding, and Yield
Performance in Field-Grown Adzuki Bean
(Shinya Kasajima, Hirotake Itoh, Yasuo Nakamaru, Hozumi Yoshida, Hitoshi
Sato) ..

230
Bio-oil
1. Analysis of Genes Expressed during the Early Maturation of Sesame Seeds
(Motonobu Yoshida, Akihiro Kishikawa, Takayuki Nakano, Eiji Tanesaka)

235
2. Effects of Different Seeding Dates on Pattern of Internode Length in Sorghum
Variety Kazetachi
(Akihiro Fujii, Satoshi Nakamura, Mitsuo Saito, Yusuke Goto) ..............................

239

3. Pranajiwa as Raw Material for Bio-Oil
(Endang Yuniastuti, Susanti Indriya Wati)

244
Vegetables
1. Selection and Evaluation Characteristics of Six Candidate Varieties of Cucumber
(Cucumis sativus) in the Dry Season Planting
(ST Rahayu, U Sumpena, Ali Asgar) ......................................................................

249

xvi Proceedings of The 7
th
2. Blue Light Induced the Stem Growth in Vegetable Water Spinach
(Futoshi Sasaki, Mikio Sekinuma, Futoshi Kato, Naoto Inoue) ..............................

252
3. Effects of Genotypes and Storage Time on Quality Parameters of Chinese
Flowering Cabbage (Caisim) Planted in Subang
(ST Rahayu, R Kirana) ..

256
4. Influence of Organic Fertilizer on Growth and Vitamin E Content of Traditional
Vegetable, Codonopsis lanceolata
(Futoshi Kato, Naoto Inoue, Seishi Yoshida)

263

Potato and Tuber
1. Review on the Effect of Postharvest Treatment on Potato Quality
(Ali Asgar) ..............................................................................................................

269
2. Perception, Attitude and Factors Influencing Households Acceptance to
Transgenic Late Blight Resistant Potatoes
(Asma Sembiring, Eri Sofiari) .................................................................................

274
3. Relations Between the Amyloplast Sedimentation in Tubers and the
Morphogenesis of Tubers in Yams
(Michio Kawasaki, Seito Hosokawa, Hayuru Yoshida, Kyoko Takahashi, Hiroki
Suto) .........................................................................................................................

279

4. Optimalising Potato Productivity in Sembalun Highlands, Nusa Tenggara Barat
Indonesia
(Baiq Nurul Hidayah, Sudjudi, Lia Hadiawati, Dwi Praptomo Sudjatmiko, Peter
Dawson, Terry Hill, Julie M. Warren) ........................................................................

282
Fruits and Flowers
1. Transformation and Transient Ekspresion Analysis of L-HBsAg DNA in Fruits of
Musa acuminata Colla cultivar Ambon Lumut and Mas using Agrobacterium
tumefaciens
(Sony Suhandono, Lailatul B, Ernawati Giri R, Putri DU, Dina RR, Ima MZ) ..........

287
2. The Study and Early Evaluation of Resistance of Banana Accessions for Wilt
Disease Caused by Fusarium oxyporum f.sp. cubense VCG 01213/16 (TR4)
(Agus Sutanto, Sudarsono, Dewi Sukma, Catur Hermanto) ...................................

291
3. Response of Plant Roots to Drought Stress
(Atsushi Kato, Saki Hoshiyasu, Akiho Yokota, Kinya Akashi) ................................

296
4. Growth and Development Characteristics of Hoya multiflora Blume
(Sri Rahayu)

300
5. Effects of High Water Table and Waterlogging on Sunflower Growth, Yield and
Seed Quality
(Satoko Yasumoto, Yukari Terakado, Morio Matsuzaki)

305
6. Population Genetics of Hoya multiflora at Sukamantri of Gunung Salak, West
Java, Indonesia Based on Isozyme Analysis
(Sri Rahayu, Rochadi Abdulhadi) .

310

th
ACSA Conference 2011 xvii

Spices
1. Endophytic Bacteria as an Alternative Agent for the Biological Control of Plant
Parasitic Nematodes on Black Pepper
(Abdul Munif, Rita Harni, Siswanto) ........................................................................

315
2. The Effect of Organic and Inorganic Fertilizers on Growth and Yield of Red Ginger
(Zingiber officinale Rosc.)
(Rudiyanto, Tri Muji Ermayanti) .

319
3. Growth Analysis of Superior Clones of Temulawak (Curcuma xanthorrhiza Roxb.)
Grown with Organic Fertilizers
(Bambang Pujiasmanto, Samanhudi) ....................................................................

324
Forage
1. Effect of Drought and Inoculation of Arbuscular Mycorrhizal Fungi in Enhancing
Productivity and Tolerance Mechanism of Grasses
(PDMH Karti, L Abdullah, J Nulik, Nurhayati, OR Nahak, S Nofyangtri) .................

331
2. The Cooling Effect of Forage Crop, Kudzu (Pueraria lobata) Vine Covering over
Livestock Buildings
(Takuya Koyama, Mika Yoshinaga, Kei-ichiro Maeda, Akira Yamauchi .................

335
3. Effect of Weed Control Management on Herbage Yield and Quality in the
Established Dwarf Napiergrass (Pennisetum purpureum Schumach)
(Renny Fatmyah Utamy, Yasuyuki Ishii, Sachiko Idota, Lizah Khairani) ................

340
4. Effect of Density of Mother Plants on Efficiency of Nursery Production in Dwarf
Napiergrass (Pennisetum purpureum Schumach)
(Asuka Yamano, Yasuyuki Ishii, Koutarou Mori, Renny F Utamy, Sachiko Idota) .

345
5. Analysis of the Major Seed Storage Protein, 13S Globulin, in Common Buckwheat
(Fagopyrum esculentum Moench)
(Tomoyuki Katsube-Tanaka, Nadar Khan, Yusuke Takahashi, Mariko
Nakagawa) ..............................................................................................................

349
Estate and Forest species
1. Isolation of soc-tuf Gene Encoding Chloroplast Elongation Factor Tu (EF - Tu)
Protein from Sugarcane (Saccharum officinarum)
(Dhika Amanda, Sony Suhandono) .........................................................................

355
2. Endophyte Microbes from Oil Palm (Elaeis guineensis) Tissues and its Potential
as a Biocontrol for Ganoderma boninense in vitro
(Wisnu Adi Wicaksono, Rika Fithri Buana, Elizabeth Caroline Situmorang) .........

360
3. Chitinase Activities of Oil Palm Root at Early Infection of Arbuscular Mycorrhizal
Fungi
(Happy Widiastuti) ..................................................................................................

366
4. In vitro Test of Rhizosphere Chitinolytic Bacteria as a Biocontrol for Ganoderma
boninense
(Rika Fithri Buana, Wisnu Adi Wicaksono, Elizabeth C Situmorang) ....................

372
xviii Proceedings of The 7
th

5. The Effect of Mulch, Trichoderma, and Arbuscular Mycorrhizal Fungi (AMF)
Biofertilizer on the Growth of Oil Palm Seedlings Inoculated with Ganoderma
(Happy Widiastuti) ....................................................................................

377
6. The Use of RAPD Marker on Gambiers Breeding Program
(Hamda Fauza, Jamsari, Istino Ferita, Ade Noverta, Azmi Dhalimi, Ahmad
Denian, Murdaningsih H Karmana) ..........................................................................

382
7. Shorea leprosula: the Most Commercial Trees to Improve: Production-Natural
Forest Productivity
(Wahyudi, Indrawan A, Irdika Mansur, Prijanto Pamoengkas)

387

8. Patogenity Test of Two Isolates of Ganoderma on Sengon Seedlings
(Elis N Herliyana, Irfan K Putra, Darmono Taniwiryono, Hayati Minarsih) ..............

391

Pathogen
1. A PCR-based Technique for Detection Cylindrocarpon destructans, the Causal
Agent of Grapevine Black Foot Disease
(Raed A Haleem, Samir K Abdullah, Jaladet MS Jubrael) ...................................

397

Photosynthesis
1. Photosynthetic Light Reactions in C
4
Photosynthesi
(Naoya Nakamura, Yuri Nakajima Munekage, Akiho Yokota) .

403

Environmental
1. Heavy Metals Concentration in Irrigation Water, Soils and Fruit Vegetables in
Coastal Area, Kota Bharu, Kelantan, Malaysia
(ER Aweng, M Karimah, Osuhaini) ..........................................................................

407
2. The Contribution of Agriculture in a Local Greenhouse Gas Turnover
(Arief Sabdo Yuwono) .

412
3. The Influence of Global Climate Indices on Rainfall Distribution Pattern and Its
Impact on Crop Yield in Gunung Kidul, Yogyakarta, Indonesia
(Bayu D A Nugroho, Hiromitsu Kanno, Ryoji Sameshima, Hiroshi Fujii, Larry
C.M. Lopez) ..

418

Economy
1. An Input-Output Analysis of the Economic Impact for Sustainable Rural
Development in Wonogiri District, Indonesia
(Shintaro Kobayashi, Shigeki Yokoyama, Satoshi Uchida, Yoshiko Iizumi) ..

423

2. Permutation Test in Evaluating the Significance of Plants in PLS-DA Model of
Jamu Ingredients
(Farit Mochamad Afendi, Md. Altaf-Ul-Amin, Shigehiko Kanaya)

429
th
ACSA Conference 2011 xix

Index of Authors ...................................................................................................................... 435
List of Organizing Committee .................................................................................................. 439
List of Participants ................................................................................................................... 441
List of Organizers .................................................................................................................... 453
Acknowledgements ................................................................................................................. 455

xx Proceedings of The 7
th
th
ACSA Conference 2011 1
Improving Photosynthesis to Increase the Productivity of Crops

Akiho Yokota

Graduate School of Biological Sciences, Nara Institute of Science and Technology, Japan
[email protected]

Abstract

Environmentally friendly energy-producing systems that utilize natural sources of energy, such as
solar, wind, land heat, and sea waves, have been developed around the world. These new energy
systems are expected to replace fossil fuels for energy production. However, they do not assimilate
CO
2
liberated into the atmosphere artificially, nor do they produce food or feed for heterotrophs.
Thus, it would be prudent to utilize plant systems to synthesize organic matter from inorganic CO
2

with solar energy. However, there are intrinsic restrictions on plant production, one of which is the
ability of the key photosynthetic enzyme, ribulose 1,5-bisphosphate (RuBP) carboxylase/oxygenase
(RuBisCO), to fix CO
2
via photosynthesis. Photosynthesis converts CO
2
into sugars and lipids. This
process relies on biochemical energy in the forms of reduced nicotinamide adenine dinucleotide
phosphate and adenosine triphosphate, which are produced from solar energy. As a catalyst,
RuBisCO has disadvantages. It has a low reaction rate, a low affinity for its substrate, CO
2
, and it
catalyzes the oxidation and evolution of carbons in sugars as CO
2
. In addition to RuBisCO, activities
of two phosphatases have been reported to be too low to give other enzymes full play. Here, I
would like to address our successes in improving photosynthetic performance of tobacco and
potato.

-- back to Table of Content --
2 Proceedings of The 7
th
Impacts of Climate Change and Climate Variability on Productivity of
Food Grain Crops

P V Vara Prasad

Department of Agronomy, Kansas State University, Manhattan, Kansas 66506, USA
2004 Throckmorton Plant Sciences Center, Department of Agronomy,
Kansas State University, Kansas 66506, USA
Tel.: +1 785 532 3746; Fax: +1 785 532 6094
[email protected]

Abstract

Crop production is highly sensitive to changing environmental conditions. In recent years long-term
climate change and year-to-year climate variability has become a major challenge to crop
productivity. Current knowledge on effects of season-long high temperatures and elevated carbon
dioxide concentrations; and effects of short periods of high temperature stress on various
physiological, growth and yield processes will be presented and discussed. Main focus will be on
major grain crops (dry bean, groundnut, soybean, rice, wheat and sorghum). Results indicate that
above optimum temperatures will have negative impacts on reproductive processes (such as pollen
production, pollen germination, fertilization, seed numbers and individual seed weight) resulting in
lower seed yield. The beneficial effects of elevated carbon dioxide mediated through increased
photosynthesis will be negated by rising temperatures resulting in lower seed yields. Grain crops
are most sensitive to high temperature stress during micro-sporogenesis and flowering. High
temperature stress during these stages leads to loss of pollen fertility, poor pollination and
decreased fertilization, resulting in fewer seed numbers. Development high temperature tolerant
cultivars will be of prime importance for adaptation to climate change and climate variability.
However, there are several challenges to develop stress tolerance genotypes, some of these
include (a) availability of genetic variability in trait of interest; (b) development and use of efficient
and reliable screening method; (c) identification of stress tolerant genotypes; (d) understanding
physiological and biochemical mechanism(s) associated with tolerance or susceptibility; and (e)
heritability of identified trait(s) and incorporation of tolerant traits into existing high yielding
genotypes. Genetic variability exists in high temperature tolerance in few grain crops. Some
physiological traits that may contribute to high temperature tolerance include increased membrane
thermostability, increased green leaf duration, higher reproductive fertility, canopy temperature
depression, increased thermal tolerance and high temperature avoidance during flowering by time
of the day of flowering. New emerging biochemical and molecular tools provides some opportunities
for screening and phenotyping. Continued collaboration between physiologists, breeders, molecular
biologists and agronomists is essential for developing strategies to combat effects of climate
change and climate variability on crop production.

Keywords: temperature stress, carbon dioxide, pollen viability, seed yield, gen

th
The Plant Improvement of Tolerance to Oxidative Stresses

Shigeru Shigeoka

Dept. Advanced Bioscience, Faculty of Agriculture, Kinki University
Nakamachi, Nara 631-8505, Japan
Tel: +81 742 43 8083
[email protected]

Summary

The explosive increase in world population and in environmental deterioration poses a serious
threat to agricultural production and food supplies. To improve food production efficiency, crops that
mature earlier with enhanced environmental stress tolerance and higher yield must be developed.
When plants are exposed to a variety of environmental stresses, excess amount of reactive oxygen
species (ROS) is generated, resulting in oxidative damage at the cellular level (J. Exp. Bot.
53,1305-1319,2002;Plant Cell Physiol. 45,1586-1594,2004). Despite their potential for causing
harmful oxidations, ROS are also powerful signaling molecules that are involved in the control of
plant growth and development as well as priming acclimatory responses to stress stimuli (Plant Cell
Physiol.51,190-200,2010; Plant Physiol.155,93-100, 2011). A wide range of strategies, including
molecular genetics and genetic engineering approaches, have been used to enhance the tolerance
of plants to abiotic stress. Many attempts have been made over the last two decades to protect
photosynthesis against stress-induced inhibition by manipulation of component antioxidant
enzymes, and an extensive literature exists showing that enhancing the capacity of the water-water
cycle through genetic engineering, including the overexpression of superoxide dismutase,
glutathione reductase, and dehydroascorbate reductase, can improve the tolerance of plants to
abiotic stress. Overall, the enhancement of chloroplast antioxidant defenses has proved to be one
of the most effective ways of protecting plant cells from abiotic stress (Biosci. Biotechnol. Biochem.
72,1143-1154, 2008, Plant Physiol. 155,93-100,2011). Transgenic tobacco plants overexpressing
thylakoid membrane-bound ascorbate peroxidase (APX) in the chloroplasts exhibited enhanced
tolerance to high-light (HL) and paraquat (PQ) treatment, a combination that is designed to
maximize photooxidative stress (Plant J. 32, 915-925, 2002). Similarly, transgenic tobacco and
tomato plants overexpressing KatE, a gene encoding an Escherichia coli catalase (CAT) in the
stroma, resulted in a greatly enhanced tolerance to photooxidative stress (Plant Cell
Physiol.41,311-320,2000; Plant Cell Environ. 26,2037-2046,2003; Plant Physiol.145,258-265,2007).
In this case, the enhanced tolerance was explained in terms of compensation for the inactivation of
chloroplastic APXs by KatE. Ectopic expression of useful genes from cyanobacteria or
Chlamydomonas (Plant J 37,12-33, 2004) into the chloroplasts of higher plants has proved to be
effective at enhancing tolerance to abiotic stress. The GPX-like proteins of Synechocystis PCC
6803 are able to reduce unsaturated fatty acid hydroperoxides using NADPH as an electron donor,
but not GSH and TRX (Plant Physiol., 136, 2855-2861, 2004). The expression of Synechocystis
GPX in Arabidopsis chloroplasts resulted in a suppression of photoinhibition and an increased
tolerance to photooxidative stress (Physiol. Plant 128, 251-262, 2006). Recently we have isolated
various HL and heat-shock (HS) stress-inducible genes, including a heat shock transcription factor
A2 (HsfA2), by suppression-subtractive hybridization from Arabidopsis plants. HsfA2-
overexpressing Arabidopsis (Pro35S:HsfA2) plants showed increased tolerance to combined stress
conditions, HL+ HS plus PQ treatments due to the increased expression of 46 genes, including a
large number of heat-shock proteins, APX 2 and galactinol synthase 1 and 2 (GolS1 and GolS2)
th
(Plant J. 48, 535547, 2006). Our findings indicated that HsfA2 is a key regulator in the induction of
the defense system under several types of environmental stress (Plant Cell Physiol. 51,486496,
2010; 52,933-945, 2011). Furthermore, mutant pqr-216 from an Arabidopsis activation-tagged line
showed a phenotype of increased tolerance to oxidative stress after treatment with 3 M PQ. Based
on the phenotype of transgenic plants overexpressing the genes flanking the T-DNA insert, it was
clear that enhanced expression of a Nudix (nucleoside diphosphates linked to some moiety X)
hydrolase gene, AtNUDX2 encoding ADP-ribose pyrophosphatase, was responsible for the
tolerance, resulting from maintenance of NAD+ and ATP levels by nucleotide recycling from free
ADP-ribose molecules under stressful conditions (J. Biol. Chem. 280, 25277-25283, 2005; Plant
Cell Physiol 48,1438-1449,2007; Plant Physiol.148,1412-1424,2008; 151,741-754, 2009; 152,
2000-2012, 2010; Plant J. 57,289301,2009; Plant Signaling Behavior 5,839-841, 2010). The
evidence described above confirms the importance of the antioxidative enzymes and the value of
genetically enhanced antioxidants and other defense compounds as a mechanism for stabilizing
photosynthesis in stress situations. Other metabolites can serve protective functions in chloroplasts.
Oligosaccharides such as galactinol and raffinose, which often accumulate to high concentrations,
can act as antioxidants as well as osmoprotectants in plant cells. Transgenic Arabidopsis plants
overexpressing GolS1 and GolS2, key enzymes in the synthesis of galactinol and raffinose, had
increased levels of these oligosaccharides and enhanced tolerance to enhanced oxidation caused
by exposure to paraquat, chilling, and osmotic stress (Plant Physiol. 147, 1251-1263, 2008). These
findings suggest that carbohydrates including raffinose family oligosaccharides and sugar alcohols
are present at high levels under normal and/or stressfull conditions and act as antioxidants to
protect plant cells from oxidative damage and maintain redox homeostasis (Plant Signaling &
Behavior 3, 1016-1018, 2008).

th
Salt Resistance Mechanism of Metroxylon sagu,
Starch-producing Palm

Hiroshi Ehara
a,*
, Wikanya Prathumyot
a,b
, Hitoshi Naito
c

a
Graduate School of Bioresources, Mie University, Tsu, Mie, Japan
b
Faculty of Agricultural Technology, Rambhai Barni Rajabhat University, Muang,
Chantaburi, Thailand
c
College of Life Sciences, Kurachiki University of Science and the Arts, Kurashiki, Okayama, Japan
* Corresponding author: Graduate School of Bioresources, Mie University, Kurimamachiya-cho 1577, Tsu,
Mie 514-8507, Japan.
Tel.: +81 59 231 9495; fax: +81 59 231 9495.
[email protected]

Abstract

Sago palm (Metroxylon sagu Rottb.) distributed in Southeast Asia and Melanesia grows in swampy,
peaty, and alluvial soils in areas with both fresh and brackish water where almost no other crops
grow without drainage and/or soil improvement. This palm species stores a large amount of starch
in the trunk. The starch of sago palm is processed into various basic raw materials and is receiving
attention as a sustainable energy resource as well as for use in the production of bioethanol due to
the current situation, in which competition between biofuel and food production is taking place.
However, sago palm is harvested primarily from natural forests and is considered to be an
unexploited plant. Thus, the Na
+
and some other ion concentrations in different plant parts as well
as the physiological and morphological features under NaCl treatments (86 to 342mM NaCl for 1 or
4 months in a hydroponic system) were investigated to study the salt resistance mechanism of sago
palm to develop a sustainable method of cultivation that is essential for the improvement of sago
palm as an economic plant. (1) Sago palm maintained a low Na
+
concentration in the leaflets, which
may be attributed to Na
+
storage mainly in the roots. K
+
absorption and distribution to the leaflets
may not be affected by changes in the Na
+
concentration in the roots and petioles in sago palm. (2)
Based on X-ray micro-analysis, a dense distribution of Na was observed around the endodermis of
the adventitious roots. Salt resistance of sago palm might be due to salt avoidance to mechanically
restrict an excess of Na distribution in plant tissues as well as maintain the water status in the
leaves by restricting the transpiration. (3) The development of Casparian strips in the endodermis
can be considered as an important mechanical factor relating to the avoidance mechanism for
preventing the excess influx of Na
+
into the stele and its translocation from root to shoot in sago
palm. (4) The factor limiting the photosynthetic rate under NaCl stress was the reduction in stomatal
conductance that resulted from a trade-off with the decrease in the transpiration rate to maintain the
water status in the leaves. (5) Although chlorophyll production was depressed, the absorption of
macronutrients was not inhibited by salt stress and there was no lack of materials, such as N and
Mg for chlorophyll production. The chlorophyll concentration could increase up to high levels over a
comparatively long time. These factors may account for the resistance of sago palm to salt stress
and its ability to grow even with a reduction of the growth rate.

Keywords: Casparian strip, Na
+
absorption, sago palm, salt avoidance, transpiration rate

th
Introduction

Sago palm (Metroxylon sagu Rottb.) that is distributed in Southeast Asia and South Pacific
areas grows in swampy, alluvial and peaty soils where almost no other crops can grow without
drainage or soil improvement (Flach, 1977). It supplied carbohydrates and, like banana and taro,
has long been cultivated (Barrau, 1959). This rare palm species stores a large amount of starch in
the trunk, approximately 300kg (dry wt.) per tree (Ehara 2006). The importance of sago palm as a
staple food is well recognized and the palm is still being in some areas of Southeast Asia and South
Pacific (Ehara et al., 2000). Its carbohydrate can be further processed into various basic raw
materials for food, animal feed and for industrial uses. Sago palm is one of the most important
crops for sustainable agriculture and for rural development in swampy areas of the tropics.
Since, sago palm is distributed not only in fresh water areas but also in brackish water
areas near the coast, it is considered to be salt-resistant. Flach (1977) reported that saline water
treatment up to EC values of 6 to 7 mmho/cm did not affect leaf emergence in sago palm.
However, there are few studies on the mechanisms of salt tolerance in sago palm. Thus, we
investigated the Na
+
and the other ions concentrations of different plant parts with some other
physiological features under NaCl treatment to study the absorption and distribution of Na
+
in sago
palm.

Materials and Methods

Expt 1. Seedlings at the 8th leaf stage (mean plant length: 50cm) were treated with the
culture solution lacking or containing NaCl concentrations of the rates of 86, 171 and 342mM NaCl
(0.5, 1.0 and 2.0%) in a pot filled with vermiculite for 30 days (n=3) under a 25klx at 30C and
RH75%. Kimura B culture solutions (Baba and Takahashi, 1958) containing the different NaCl
concentrations (pH5.5) were supplied every day according to the amount of solution consumed and
then they were renewed once a week. The Na
+
and K
+
concentrations in the leaflets, petioles and
roots determined using an ion chromatograph with a conductivity detector (Shimadzu CDD-6A, IC-
C2, Japan).
Expt 2. The seedlings at the 8th or 9th leaf stage were used for the NaCl treatments. The
culture solution containing 342mM NaCl was used from July 9 to August 9, 2004 in the phytotron
under natural sunlight. Ion concentration in the plant tissue was measured. A portion in the region
above the extension zone of the large roots of the treated plants was soaked in liquid nitrogen after
sampling and kept at -70C. The frozen root samples were freeze-dried and prepared as
transverse sections. The sections were coated with gold ion and used for SEM observation and X-
ray micro-analysis (Horiba EMAX-5770W, Japan).
Expt 3. At ten months after germination, the longest adventitious root was taken as
sample and preserved in 70% ethanol solution. The transverse sections of the root were prepared
as 1st position: root tip, 2nd position: 10 mm from root tip, 3rd position: 20 mm from root tip, 4th
position: 30 mm from root tip, 5th position: 40 mm from the root tip, 6th position: between the first
and second lateral roots, and 7th position: above the second lateral root. The sections were stained
according to Brundrett et al. (1988) and observed with a fluorescence microscope (Axio Imager A1;
Carl Zeiss, Germany).
Expt 4. Four spiny seedlings were selected and transferred individually to a 7.3 L plastic
pot filled with vermiculite. The mean value of plant length of all the plant materials was 79.3 cm.
Two treated pots were connected individually to the first peristaltic pump that was used to supply
Kimura B culture solution containing NaCl 224 mM (1.3% NaCl) (pH 5.5) to the treated pots for 6h
and the 2nd pump that was used to supply the culture solution without NaCl for another 6h by turns
twice a day. The 4th and 5th leaves from the top were used for the measurement of the
photosynthetic rate (Pn), transpiration rate (Tr) and stomatal conductance (Cs) by a portable
th
photosynthetic meter (Analytical Development Company limited LCA-4, England) under 900 mol
m
-2
s
-1
PAR.

Results and Discussion

Na
+
and K
+
concentrations in different plant parts
There were no significant differences in the Na
+
concentrations in the leaflets between the
three NaCl concentrations in the culture solution, the values of which ranged from 22 to 44 mol/g
(Figure 1). In the petioles, Na
+
concentrations under the 342mM NaCl treatment were significantly
higher than those in the absence of NaCl treatment (one and half times), and the differences
between the absence of NaCl treatment and the 86mM NaCl treatment, 86mM and 171mM NaCl
treatments, and 171mM and 342mM NaCl treatments were not significant. The Na
+
concentrations
in the petioles tended to be higher at higher NaCl concentrations, but with a maximum increase of
1.5 times. The Na
+
concentrations in the roots were significantly higher at higher NaCl
concentrations, increasing 1.5, 2.2 and 3.1 times under the 86, 171 and 342mM NaCl treatments,
respectively. Two types of salt tolerance include an avoidance mechanism and a resistance
mechanism (Yeo and Flowers, 1983). Through the avoidance mechanism, a low Na
+

concentrations maintained in the leaf blade. Sago palm can be considered to display an avoidance
mechanism to maintain a low Na
+
concentration in the leaflets by storing Na
+
in the roots and
petioles. The K
+
concentrations in the leaflets, petioles and roots did not show any significant
differences at three NaCl concentrations in the culture solution and in the absence of NaCl
treatment, which seems very important to understand the mechanism of salt tolerance in sago palm
(Figure 1). K
+
accumulation may be associated with osmotic adjustment in sago palm.

Na
+
concentration in different parts of the roots
The Na
+
concentration in the roots increased with the NaCl treatment (Figure 1). In the
adventitious roots, the Na
+
concentration was lower in the stele than in the cortex (Figure 2). Figure
3 shows the Na distribution from the cortex to the stele in the adventitious roots of the treated plants
based on X-ray micro-analysis. The amount of Na was larger in the cortex than in the stele. A
dense distribution of Na was observed in the inner region of the cortex near the endodermis. Based
on our present findings, it appeared that the region with the endodermis was able to trap some of
the excess influx of Na into the large roots. This mechanism must be very important to restrict the
translocation of Na
+
from root to shoot under salt stress.

Different letters in the figure indicate significant differences (0.05 probability level, Tukey-Kramer test).

Figure 1. Na
+
and K
+
concentrations in leaflets (L), petioles (P) and roots (R) in different NaCl treatments (0, 86,
171 and 342mM).

0
50
100
150
200
250
300
350
400
N
a
c
o
n
c
e
n
t
r
a
t
i
o
n

(
m
o
l

g

-
1
)
L P R

L P R L P R L P R
0

86

171

342

A
B
C
D
a
ab
bc c

0
100
200
300
400
500
600
700
800
K
c
o
n
c
e
n
t
r
a
t
i
o
n

(
m
o
l

g

-
1
)
L P R

L P R L P R L P R
0

86

171

342

th

Casparian strip in the root
We found that the Casparian strip was located in the endodermal cell wall of both
adventitious roots of sago palm (Figure 4). Taking into account the previous findings of Ehara et al.
(2008) that a dense distribution of Na was observed around the endodermis in the extension zone
of the adventitious root, therefore, the Casparian strip develops in the endodermis of which can be
considered as one of the important mechanical factors relating to functional role of the avoidance
mechanism for preventing the excess influx of Na
+
through an apoplastic pathway into the stele and
its translocation from root to shoot in sago palm.

Different letters in the figure indicate significant differences in
different parts (0.05 probability level, Tukey-Kramer test). Asterisks
indicate significant difference in each part (0.05 probability level, T-
test).

Figure 2. Na
+
concentration in different parts of the roots.

0
100
200
300
400
500
600
700
Cortex Stele Small
root
Cortex Stele Small
root
N
a
+

c
o
n
c
e
n
t
r
a
t
i
o
n

(
m
o
l

g
-
1
)
a
b b
*
*
*
Treated plants Control plants
Cortex Stele Lateral
of Adventitious root
root
Cortex Stele Lateral
of Adventitious root
root

300m
11 Na K
Full scale [cps]
500
S C C S
C C S En En
300m
11 Na K
Full scale [cps]
500
S C C S
300m
11 Na K
Full scale [cps]
500
300m
11 Na K
Full scale [cps]
500
S C C S
C C S En En
C: cortex
S: stele
: indicates the
outline of
endodermis
En: endodermis

Figure 4. The structure and component of adventitious root at 10 mm from the root tip under visible light (left)
and UV (right) microscope. Arrowheads indicate Casparian strips in the radial cell walls of
endodermis. Co: cortex, En: endodermis, Pe: pericycle, Ph: phloem, Xy: xylem.

5
550
00
m
mm
X
XXy
yy
P
PPh
hh
P
PPe
ee
En
C
CCo
oo
50 m
Xy
En
Co
Figure 3. SEM of adventitious root and Na distribu-
tion based on X-ray micro-analysis.
th
Photosynthetic rate and related characteristics
After the 4th week of the treatment, the SPAD value of the control plants started to
increase and became stable after the 6th week (Figure 5). Due to the slow rate of increase in the
SPAD value of the treated plants, the difference in the SPAD value between the control and treated
plants became more appreciable in the 5th to 7th week and gradually decreased after the 7th week.
Finally, the SPAD value of the treated plants reached nearly the same level as that of the control
plants. The SPAD value is a parameter positively related to the chlorophyll concentration in plant
leaf or chlorophyll content per unit leaf area. Therefore, it can be suggested that the rate of increase
in the chlorophyll concentration of the treated plants also may be low. Based on this result, it can be
suggested that sago palm is able to produce chlorophyll even under NaCl stress, although the rate
of chlorophyll production was low. The important structural components of chlorophyll are
magnesium and nitrogen that are located in the centre of chlorophyll (Lack and Evans, 2001). We
found that the total N and Mg
2+
concentrations of the leaflets did not display any distinct differences
between the control and treated plants, and it was therefore clear that the deficiency of N and Mg
was not the cause of the low chlorophyll production.
14th leaf
0
20
40
60
80
0 2 4 6 8 10 12 14 16 18
Duration (week)
S
P
A
D

v
a
l
u
e

.

Figure 5. Changes in SPAD value of the leaflets at the 14th leaf of the control plants (C1, C2) and treated plants
(T1, T2) during the NaCl treatment. Open and close symbols indicate the control and treated plants,
respectively. Circle and triangle symbols indicate plant replication No. 1 and 2 of the control and
treatment.

The photosynthetic rate, transpiration rate and stomatal conductance in both leaves of the
treated plants decreased by 40%, compared to the value of the control plants (Figure 6). Based on
the water content, which was not appreciably different between the control and NaCl treatment, it is
suggested that a decrease in the stomatal conductance, which leads to the decrease in the
transpiration rate and also to the decrease in the photosynthetic rate is the mechanism that sago
palm used to avoid water loss and maintain the water status in the plant body under saline
conditions. The decrease in the photosynthetic rate can be interpreted as a trade off with the
decrease in the transpiration rate. The decrease of the photosynthetic rate might be caused by 2
main factors, i.e. reduction in the stomatal conductance and low chlorophyll production in the
leaves.
In conclusion, sago palm growing under NaCl treatment can maintain a low Na
+

concentration in the leaflets by storing Na
+
mainly in the roots and petioles at lower leaf positions
with a fair reduction of the growth rate. This accounts for the slow morphogenesis and the decrease
in the stomatal conductance and results from the maintenance of the water status in the plant body.

th

0.00
0.02
0.04
0.06
0.08
C
s

(
m
o
l

m
-
2
s
-
1
)
0.0
0.5
1.0
1.5
T
r

(
m
m
o
l

m
-
2
s
-
1
)
0
2
4
6
8
10
P
n

(
m
o
l

m
-
2
s
-
1
)
C1
4th leaf 5th leaf
C2 T1 T2 C1 C2 T1 T2

Figure 6. Photosynthetic rate (Pn), transpiration rate (Tr) and stomatal conductance (Cs) of the 4th and 5th
leaves from the top of the control plants (C1, C2) and treated plants (T1, T2) at 900 PAR in October
2007.

References

Baba, I. and Y. Takahashi 1958. Solution Culture. In: Sakumotus Shiken Ho (Togari, Y. ed.) Nogyo Gijutsu
Kyokai, Tokyo. 327343.
Barrau, J. 1959. The sago palm and other food plants of Marsh Dwellers in the South Pacific Islands. Econ. Bot.
13: 151159.
Ehara H, H Shibata, W Prathumyota, H Naito, H Miyake. 2008. Absorption and distribution of Na
+
, Cl
-
and some
others ions and physiological features of sago palm under salt stress. Trop.Agr.Develop. 52:7-16.
Ehara, H. 2006. Geographical distribution and specification of Metroxylon palms. Jpn J Trop. Agr. 50: 229233.
Ehara, H., S. Susanto, C. Mizota, S. Hirose and T. Matsuno 2000. Sago palm (Metroxylon sagu, Arecaceae)
production in the eastern archipelago of Indonesia: Variation in morphological characteristics and pith-
dry matter yield. Econ. Bot. 54: 197206.
Flach, M. 1977. Yield potential of the sago palm and its realization. In: Sago-76: The Equatorial Swamp as a
Natural Resource (Tan, K. ed) Papers of the 1st International Sago Symposium, Kuala Lumpur. 157
177.
Lack, A.J. and D.E. Evans 2001. Instant notes in plant biology. BIOS Scientific Publishers, London. Pp.332.
Yeo A. R. and T. J. Flowers 1983. Varietal differences in the toxicity of sodium ions in rice leaves. Physiol. Plant.
59: 189195.
th
How to Increase Food Crop Productivity in Asia

Narasim Upadyayula

Monsanto Singapore Co (Pte) Ltd
Singapore. Tel.: +65 97220310; fax: +65 64885610
[email protected]

Abstract

At Monsanto we believe that by improving agriculture, we improve peoples lives. In the hands of
farmers, better seeds along with good agronomic practices can help meet the needs of our rapidly
growing population. We believe that we need to increase productivity while protecting the Earths
natural resources. Monsantos technologies are striving to make agriculture truly sustainable by
getting more from each acre, each raindrop and each seed. In this presentation I will talk about the
3 main pillars that we think we can help us increase the productivity by using less resources: (1)
Breeding, (2) Agronomic Practices, and (3) Biotechnology.

th
Biosynthesis of Nicotine as an Anti-insect Defense in Plants

Takashi Hashimoto

Graduate School of Biological Sciences, Nara Institute of Science and Technology,
630-0192 Nara, Japan
[email protected]

Abstract

Nicotine and related pyridine alkaloids are synthesized in the root and then transported to the aerial
parts of tobacco plants. Expression of biosynthetic genes for these alkaloids is enhanced 3-4-fold
upon insect herbivory to the leaf. Current model suggests that jasmonate acts as a transmissible
signal from the damaged leaf to the underground part, where it activates structural genes of nicotine
biosynthesis via the conserved COI1-JAZ-MYC2 pathway. In Arabidopsis, the MYC2-family basic-
helix-loop-helix transcription factors mediate transcriptional regulation of jasmonate-responsive
genes, and their transcriptional activities are suppressed by physical interactions with Jasmonate-
ZIM domain (JAZ) suppressors. Regulatory NIC loci that positively regulate nicotine biosynthesis
have been genetically identified and their mutant alleles have been used to breed low-nicotine
tobacco varieties. The NIC2 locus comprises tandemly arrayed transcription factor genes of an
Ethylene Response Factor (ERF) subfamily; in the nic2 mutant, at least seven ERF genes are
deleted altogether. Overexpression, suppression, and dominant-repression experiments using
transgenic tobacco roots showed functional redundancy and divergence among the NIC2-locus
ERF genes. These transcription factors recognized a GCC-box element in the promoters of nicotine
pathway genes, and specifically activated all known structural genes in the pathway. We also
demonstrate that tobaccoMYC2 controls nicotine biosynthesis genes in two combinatorial ways, by
directly binding G-box in the target promoters, as well as by up-regulating the NIC2-locus ERF
genes.

th
Food Security and Agriculture Biotechnology Progress in Indonesia

Tantono Subagyo, Fadlilla Dewi Rakhmawaty

Syngenta Indonesia, Perkantoran Hijau Arkadia, Tower C, 8FL Jakarta

Abstract

Food security in Indonesia become serious problems because land conversion from agriculture is
high and almost uncontrollable and the population growth rate is still high, the conditions worsened
by climate uncertainty. One of the answer to this problems is to increase yield and it can be
achieved by increasing seed quality using available technology. Although it is not panacea,
biotechnology can provide tools to increase seed quality. Biotechnology research in Indonesia is
done since 1980 but so far little products come to the market due to the regulations. Recent
improvements in the system and regulations make the product pipeline moving, and it is hoped that
the first launch of transgenic plants happen in 2012. However some improvements is still needed in
order to make regulations in Indonesia facilitating biotechnology development.

th
14-3-3 Proteins Act as Intracellular Receptors for Rice Hd3a Florigen

Hiroyuki Tsuji
1
, Ken-ichiro Taoka
1
, Izuru Ohki
2
, , Kyoko Furuita
2
, Kokoro
Hayashi
2
, Tomoko Yanase
1
, Midori Yamaguchi
1
, Chika Nakashima
1
, Yekti Asih
Purwestri
1,
, Shojiro Tamaki
1
, Yuka Ogaki
1
, Chihiro Shimada
1
, Atsushi
Nakagawa
3
, Chojiro Kojima
2,3
and Ko Shimamoto
1

1
Laboratory of Plant Molecular Genetics, Nara Institute of Science and Technology,
8916-5 Takayama, Ikoma, Nara 630-0192, Japan
2
Laboratory of Biophysics, Graduate School of Biological Sciences, Nara Institute of Science and Technology,
8916-5 Takayama, Ikoma, Nara 630-0192, Japan
3
Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Suita, Osaka 565-0871, Japan
Present address: Faculty of Biology, Universitas Gadjah Mada, Yogyakarta 55281, Indonesia

Abstract

Florigen was proposed 75 years ago to be synthesized in the leaf and transported to the shoot
apex, where it induces flowering. Only recently have genetic and biochemical studies established
that florigen is encoded by FLOWERING LOCUS T (FT), a gene that is universally conserved in
higher plants. Nonetheless, the exact function of florigen during floral induction remains poorly
understood and receptors for florigen have not been identified. We show here that the rice FT
homologue Hd3a interacts with 14-3-3 proteins in shoot apical cells, yielding a complex that
translocates to the nucleus and binds to OsFD1, a rice homologue of Arabidopsis FD. The resultant
ternary 'florigen activation complex' (FAC) induces transcription of OsMADS15, a homologue of
Arabidopsis APETALA1 (AP1), which leads to flowering. We determined the 2.4- crystal structure
of a rice FAC. The modelled FAC structure provides a mechanistic basis for florigen function in
flowering. Our results suggest that 14-3-3 proteins act as intracellular receptors for florigen in shoot
apical cells and offer new approaches to manipulate flowering in various crops and trees.

th
Food Security and Sustainable Agriculture

Paul P.S. Teng

S Rajaratnam School of International Studies
Centre for non-Traditional Security Studies (RSIS/CNTS)
and
National Institute of Education, Nanyang Technological University, Singapore 637616
[email protected]

Abstract

Food security is a complex interplay of forces and is more than just an issue of supply and demand.
Various definitions have been proposed but in general most consider access to safe food which is
nutritious at all times to all people. Four dimensions of food security have been proposed in a
conceptual model by RSIS/CNTS, namely food availability, physical access, economic access and
utilization. While each dimension is necessary for overall food security, they likely have different
weightings in a rural setting as compared with an urban setting and also across countries with
different incomes and net food trade balances. Food availability, the first dimension of food security,
addresses the supply side and is determined by the level of food production, stock levels, food aid
and net trade. Raising farm productivity is a core issue; whether by accessing or increasing inputs,
improving seed varieties, or employing better farm management practices. Herein also lays the
interplay with sustainable agriculture, as raising farm productivity has the potential to clash with
sustainable agriculture goals. Food security implies surplus production over demand so that the
excess may be sold or traded with food deficit households. If Sustainable Agriculture is taken to
mean agriculture which is environmentally friendly, economically sound and socially just, then
ensuring food availability means ensuring that there is sustainable agriculture. A key debate is the
use of appropriate technology and the modality in which it is practiced, whether in a conventional
manner or through organic and subsistence farming. The debate is further complicated by the fast
uptake of biotechnology crops. Food availability is often the focus of much of the debate on food
security but raising farm productivity alone is not sufficient to ensure household food security. The
second dimension is the physical access to food. This means an adequate amount of food must be
within the physical reach of vulnerable households, whether through their own production or through
the marketplace, to assure food security. Common threats to physical access to food are war, civil
strife, poor infrastructure, inadequate logistics for food distribution and market imperfections. The
third dimension is economic access to food or the ability of the household to purchase the food it
requires. As the most recent food crisis demonstrated, urban households were among the hardest
hit as they saw their purchasing power decline drastically and they had very limited capacity to
produce their own food. Additional factors that will influence economic access include employment
and income security, macroeconomic policies and social security programmes. The fourth
dimension in food security is food utilization, typically reflected in the nutritional status of an
individual and is determined by the quantity and quality of dietary intake, food safety and human
health factors. Strategies to combat food insecurity arising from this dimension include bio-
fortification of common staples through conventional or bio-technology. In the longer term, food
security considered as a four-dimensional complex, is inextricably linked to sustainable agriculture,
th
which in an Asian context, must take into account the millions of smallholder farmers and the
millions of urban poor.

Keywords: food security, sustainable agriculture

th
Improvement of Oil Palm Productivity

Tony Liwang

Plant Production & Biotechnology Division,
PT SMART Tbk, BII Plaza, Tower 2, 10
th
Fl., Jalan M.H. Thamrin 51, Jakarta, Indonesia.
[email protected]

Abstract

Since 2009 Indonesia is the largest palm oil producer in the world. At the same time, Indonesia
became the largest oil palm seed producer as well as consumer in the world. However, some major
challenges facing in oil palm upstream industries in Indonesia are a narrow basic of genetic
material, a long period needed for breeding cycle, limited human resources and research findings,
and a limited genetic source for abiotic as well as biotic stress in some specific areas, and low
absorption efficiency of nutrition. This paper explains the main research activities to improve the oil
palm productivity. To enlarge and enrich the oil palm germplasm in Indonesia, a consortium of oil
palm companies has carried out some explorations, such as to Cameron, Angola, and others
countries. Moreover, the application of new gene resources has been studied for the phenotypic
characters, genetic diversities and heterosities by using molecular markers. Elite varieties of oil
palm could be obtained faster by the application of micro satellite and Single Nucleotide
Polymorphism (SNP) markers from DNA genome sequences of selected genotype in early phase.
The application and commercialization of oil palm tissue culture were the big challenge for the
industry to improve the oil palm productivity at large scale, it might be included the clone of elite oil
palm and DxP bi clonal seedlings with 20-30% higher of productivity compared to conventional oil
palm. The originality of ramets could be done by using DNA fingerprinting. Genetic engineering
technology focused on water stress tolerant, resistance to Ganoderma sp. and oil synthesis.
Subsequently, the techniques of anther culture to produce dihaploid homozygous plant as a pure
line will be used as a parental for F1 Tenera hybrid in order to produce oil palm with two to three
times higher productivity compared to conventional oil palm.

Key words: oil palm, Elaeis guineensis Jacq, biotechnology, tissue culture, productivity

th

th
Characterization of Water Availability, Management Practices and Grain
Yield for Deepwater Rice in Northwest Cambodia

Nguyen T.B. Yen
a
, Akihiko Kamoshita
a,*
, Yuji Araki
a,b
, Makara Ouk
c

a
Asian Natural Environmental Science Center, The University of Tokyo, Japan
b
Faculty of Education, Saitama University, Saitama, Japan
c
Cambodian Agricultural and Development Institute, Phnom Penh, Cambodia
*Corresponding author: Asian Natural Environmental Science Center,
The University of Tokyo, 1-1-1 Midoricho, Nishitokyo, 188-0002 Japan.
Tel/fax.: +81-42-463-1696.
[email protected]

Abstract

This study aimed to characterize rice area from the shallower (lower toposequence of) rainfed lowlands side to
the deeper floating rice side in Northwest Cambodia during wet season rice (WSR) production in 2009 and 2010
for the yearly and spatial differences in field water conditions, management practices and grain yield. This area
considered as deepwater rice (DWR) area was divided into three groups with (1) upper fields located near the
National Road Number 5 (referred as ULR); (2) middle fields (referred as MLR and MFR where lowland rice (LR)
and floating rice (FR) were planted, respectively); and (3) lower fields located near to the Lake (referred as LFR).
Water came to the paddy fields from both the inundation from Tonle Sap Lake and rainfall in WSR 2009, but
only from rainfall in WSR 2010. Water depths increased from upper to lower fields in 2009, while they were
shallower and relatively similar between the field locations in 2010. Broadcasting time started earlier and
harvesting time finished later in FR fields than in LR fields. The overall average grain yield for both years of 2009
and 2010 was low. The lowest yields were observed in MLR and MFR in 2009 as well as they were in MFR and
LFR in 2010. Lower yield in WSR 2009 was mainly due to the water shortage at heading stage for both FR and
LR, improper application of N fertilizer and insufficient weed management for LR, and late sowing for FR. Lower
yield in WSR 2010 was mainly due to low water level for FR, low N fertilizer rate and insufficient weed
management. This study identified important spatial and yearly variation in rice management and grain yield for
farmers to cope with unpredictable flooding environments in DWR area.

Keywords: Cambodia, deepwater rice, flooding pattern, rice type

Introduction

In Cambodia, deepwater rice (DWR) areas are located in the provinces near to the Tonle
Sap Lake, the Mekong River, and Tonle Bassac River. In 1960s, the DWR area occupied up to 16%
of Cambodias rice land (about 400,000 ha) (Javier, 1997; Seng et al, 1988). However, as the
discouragement of growing DWR during Pol Pot regime, DWR area decreased sharply and it was
only 120,000 ha in 1988 (Seng et al., 1988). DWR presented 3.9% of the cultivated area in 2006
(MAFF, 2006). Cambodians Tonle Sap Lake (TSL) floodplain is well known for its unique dynamic
flooding pattern between dry and rainy season. Volume of the Lake ranges from about 1.3 to 75
km
3
, its surface area varies from 2,500 to about 15,000 km
2
, and its water level increases from 1.4
to 10.3 m above sea level, between dry and rainy season (MRC, 2010a). DWR is important source
of livelihood to many poor villages in the TSL floodplain that do not have access to better
agricultural land higher up. There is a need to further increase the productivity of DWR in order to
improve the local farmers livelihood and to conserve the DWR area. However, necessary
information for yield improvement in DWR area such as flooding pattern, land use pattern,
management practices in Cambodia are not sufficient. We conducted a study to quantify the yearly
and spatially difference in field water condition in DWR area in Northwest Cambodia, and to assess
rice management practices and grain yield in the area.
th

The study was carried out at a DWR area inside a flood plain area of TSL located in
Kampong Preah village, Kampong Preah commune, Sangke district, Battambang province,
Northwest Cambodia in 2009 and 2010. Eighty five fields (91.2 ha in planting area) were selected
which were located continuously along a transect line from a toposequentially upper zone nearby
National Road Number 5 toward TSL. These 85 fields were divided into three groups according to
their field locations : (1) upper fields located closer to the National Road Number 5 where only LR
was grown (19 fields; 11.4 ha) and referred as ULR; (2) middle fields where both LR and FR were
grown (19 fields; 31.6 ha) and referred as either MLR or MFR; and (3) lower fields located near to
the Lake where only FR was grown (37 fields; 48.2 ha) and referred as LFR. Variety, field size and
type of rice were determined for the 85 fields in WSR 2009 and 2010. Thirty fields within the 85
fields were selected from each field group; sowing time, mid-season tillage practice, fertilizer input,
pest control and grain yield were determined by the interviews to the owners in ending time of each
WSR.


Field water environment
Field water regime of the studied area in WSR 2009 was completely different from that in
WSR 2010 (Figure 1). In WSR 2009, water came to the fields from both the inundation from the
Tonle Sap Lake and rainfall. Flood started earliest in lower fields in September, then middle and
upper fields afterward. Flood started receding to the Lake in late October and rice fields became
non-flooded conditions in middle fields and upper fields in late November and in lower fields in early
to mid December. There was large difference in water depth between the 3 field locations in 2009.
Rice ecosystems of the three locations could be classified as DWR for middle and lower fields and
medium-deep rainfed lowland rice for upper fields (Mackill et al., 1996). In WSR 2010, water came
to the fields only from the rainfall; field water regime was relatively similar to all the 3 field locations
with the average maximum water depths less than 30 cm in mid October. These water conditions in
2010 were more favorable for rainfed lowland rice than floating rice. Low water level in Tonle Sap
Lake leading to shrink floodplain area in 2010 was probably due to extremely low water level in
Mekong River (IRIN news, 2010) which was caused likely by a combination of an early end to the
2009 wet season, low monsoon rainfall and very low rainfall in the dry season in upper Mekong
Basin (MRC, 2010b).

Management practices
Crop calendar
Planting season for FR fields is earlier than that for LR fields. For FR fields, farmers start
land preparation from early March to late April (Figure 1). Dry seeds with rate of about 100 kg ha
-1

are broadcasted mainly from early April to early May. Farmers sometimes have to broadcast seeds
for the second time in late May or early June if rice establishment failed due to drought. For LR
fields, land preparation is often from mid April to mid May. Dry seeds with higher rate in comparison
with FR (150 kg ha
-1
) are broadcasted from mid May to mid June. Rice is harvested from early
December to early February in FR fields and from late November to early January in LR fields, both
depending on maturity type of rice varieties.

Distribution of rice type and varieties
LR and FR were both grown in the studied area in the both WSR 2009 and 2010. In
general, early medium varieties of LR were only planted in upper fields while medium varieties of
LR were planted in both upper and middle fields. Early varieties of FR were only planted in middle
th
fields while medium and late varieties of FR were planted in both middle and lower fields. In
comparison between WSR 2009 and 2010, there was a small change in the area ratio of LR and FR
in middle area. Area of LR decreased from 38% in WSR 2009 to 30% in WSR 2010 but area of FR
increased from 62% in WSR 2009 to 70% in WSR 2010. Among the varieties planted in the studied
area, early varieties of FR in the middle area had the largest increase in area percentage, from 22%
in WSR 2009 to 47% in WSR 2010.
0
50
100
150
200
250
W
a
t
e
r

d
e
p
t
h

(
c
m
)
0
20
40
60
80
100
120
R
a
i
n
f
a
l
l

(
m
m
)
0
50
100
150
200
250
W
a
t
e
r

d
e
p
t
h

(
c
m
)
0
20
40
60
80
100
120
R
a
i
n
f
a
l
l

(
m
m
)
rainfall upper (LR)
middle ( LR & FR) lower (FR)
Land preparation
Sowing
Heading
Harvesting
Land preparation
Sowing
Heading
Harvesting
FR
LR
Rainfall: 1,356 mm, 89 days
Jan Feb Mar Apr May Jun Jul Aug Sept Oct Nov Dec
(a)
(b)
(c)
0
50
100
150
200
250
W
a
t
e
r

d
e
p
t
h

(
c
m
)
0
20
40
60
80
100
120
R
a
i
n
f
a
l
l

(
m
m
)
0
50
100
150
200
250
W
a
t
e
r

d
e
p
t
h

(
c
m
)
0
20
40
60
80
100
120
R
a
i
n
f
a
l
l

(
m
m
)
rainfall upper (LR)
Land preparation
Sowing
Heading
Harvesting
Land preparation
Sowing
Heading
Harvesting
FR
LR
(a)
(b)
0
50
100
150
200
250
W
a
t
e
r

d
e
p
t
h

(
c
m
)
0
20
40
60
80
100
120
R
a
i
n
f
a
l
l

(
m
m
)
0
50
100
150
200
250
W
a
t
e
r

d
e
p
t
h

(
c
m
)
0
20
40
60
80
100
120
R
a
i
n
f
a
l
l

(
m
m
)
rainfall upper (LR)
Land preparation
Sowing
Heading
Harvesting
Land preparation
Sowing
Heading
Harvesting
FR
LR
(a)
(b)
Land preparation
Sowing
Heading
Harvesting
Land preparation
Sowing
Heading
Harvesting
FR
LR
(a)
(b)
(c)

(a) and WSR 2010 (b), and cropping calendar for FR and LR (c) in the studied area. The error bars indicate standard deviations.

Figure 1. Rainfall distribution and water depth in the 3 field locations (upper, middle and lower) in WSR 2009.

Relationship between grain yield, environmental and management factors
In WSR 2009, grain yields of ULR and LFR (120 and 164 g m
-2
, respectively) were
significantly higher than those of MLR and MFR (50 and 56 g m
-2
, respectively). However, grain
yields of ULR and MLR (both 262 g m
-2
) were significantly higher than those of MFR and LFR (87
and 111 g m
-2
, respectively) in WSR 2010.
Average grain yield of both WSR 2009 and 2010 was low with only 180 g m
-2
for LR and
110 g m
-2
for FR. The lowest yields were observed in MLR and MFR in WSR 2009 which was due
to risky water environments in middle fields. With maximum water depth of 85 cm and absence of
standing water after late November (Figure 1), the water condition in this area was too deep for LR
for a possible submergence damages and insufficient for medium and late maturing FR to maintain
good grain filling. This was also supported by the positive correlation between maximum water
depth and grain yield for FR and negative correlation between those for LR (Table 1). Farmers
responded to this risky water condition by changing rice type/varieties from year to year based on
yield obtained from previous year. The increase in area of early variety of FR in WSR 2010 was due
to that farmers observed that yields of early variety of FR in middle fields were higher than other
varieties of LR and FR in this area (data not shown).
Low yield in WSR 2009 was mainly due to (1) the water shortage at heading stage for both
FR and LR, (2) non- or late application of N fertilizer for LR, (3) insufficient weed management for
th
LR and (4) late sowing for FR (Table 1). (1) Due to low rainfall occurring at pre-flood period (June to
August; Figure 1a) in WSR 2009, rice plants suffered drought stress leading to delayed heading,
mainly from late November to mid December while there was also low rainfall in the late season.
This caused the shortage of water at heading stage of 10 out of total 29 fields. Those fields where
rice plants did not suffer drought at late stage were mainly located in lower part, or bunded with high
levees, or pumped water from the water source nearby. This indicated that well-water management,
especially at heading stage, is crucial to improve yield in DWR area, particularly in middle and
upper fields. (2) In WSR 2009, LR plants were likely submerged during high flood (40 cm in upper
fields and 85 cm in middle fields), growing situation of rice plants before flood commence was very
crucial for gaining high grain yield. Taller and more vigorous rice plants, which could be improved by
basal application of N fertilizer (before flood commence), were able to withstand submergence and
hence gave higher yield and this was also indicated in Puckridge (1991). It was suggested that rice
plant should be able to uptake more than 20 kg N ha
-1
before onset of flooding in order to reduce
yield loss due to submergence (Puckridge, 1991) while Sharma and Gosh (1998) reported that
optimum basal fertilizer rate for semi-deep water environment was 30 kg N ha
-1
. The average N
fertilizer applied in LR field in WSR 2009 was less than half of this recommendation rate (4-15 kg N
ha
-1
; data not shown). (3) Our study showed that conducting midseason tillage practice, a weed
control method, helped to improve yield of LR in WSR 2009. All of LR fields were conducted the
practice in WSR 2010 while about half of LR field number were not conducted in WSR 2009, which
was perhaps due to water constraint (drought or flood at the time farmers wanted to do the
practice). (4) Late sowing significantly decreased yield of LFR. High rainfall occurred mainly from
late April to mid May while only few rains with small amount occurred in June and July (Figure 1a).
This might be the reason leading the poor establishment of crop with late sowing. When the flood
arrived, this late sowing rice was likely more susceptible to the rapidly rising water in September.
The importance of sowing in time was also mentioned by Catling (1983), Javier (1997) and Sing et
al. (2004).

Table 1. Correlation between rice yield and water condition, management factors of LR and FR in WSR 2009
and WSR 2010

*P<0.1; **P<0.05; ***P<0.01
a
values for flooded at heading stage and those for other water conditions at heading were 1 and 0, respectively, as a dummy
variable
b
values for inorganic fertilizer applied before flood commence and those for not applied or after flood commence were 1 and 0,
respectively, as a dummy variable
c
values for conducting mid-season tillage and those without the practice were 1 and 0, respectively, as a dummy variable
d
values for conducting mid-season tillage by plowing and those for conducting the practice by harrowing were 1 and 0,
respectively, as a dummy variable

th
Low yield of FR in WSR 2010 was mainly due to low water level as the discussion at
beginning of this section. Beside that insufficient weed control was also another reason. Higher
application rate of herbicide was applied in WSR 2010 in comparison with that in WSR 2009 and
low application rate of herbicide significantly reduced yield of FR in WSR 2010 (Table 1). This was
because that weed infestation was more severe throughout the crop season due to the low water
level in WSR 2010 while FR fields were not conducted midseason tillage for controlling weed like
LR. Different from WSR 2009, water condition in WSR 2010 was more favorable for growing LR like
in rainfed lowland environment. Therefore, yield of LR in WSR 2010 could be further improved by
conducting midseason tillage with plowing for controlling weed (Table 1) and increase application
rate of N fertilizer. The N fertilizer rate applied this WSR was only about one third of the
recommendation rate for rainfed lowland rice in drought or submerged prone area with rate of 60 kg
ha
-1
(Balasubramnian and Hill, 2002). However, it should be noticed that field water environment in
WSR 2010 was not representative for most years in the studied area.
In short, it is risky for farmers to attempt to increase planting higher yielding lowland rice in
the middle part of the floodplain of TSL, due to the occurrence of deep flood incidence, but farmers
could miss chances of higher yield if planting traditional floating rice varieties just to escape from
submergence damage. It is desirable if information on water situation in the area is informed to
farmers by a long-term weather forecast before the cropping season (February or March). So that
farmers will be able to make a right decision of selecting rice type/variety to grow in the area.
Beside that early maturity varieties with higher yield potential and tolerance to submergence
(suitable for medium-deep water area) can be introduced in to the area in order to improve grain
yield in a sustainable manner.

References

Catling, H.D., Hobbs, P.R., Islam, Z. and Alam, B., 1983. Agronomic practices and yield assessments of
deepwater rice in Bangladesh. Field Crops Research, 6: 109-132.
IRIN news. 2010. Cambodia: Record low water levels threaten livelihoods. [Online]. Available at
http://www.irinnews.org/Report.aspx?ReportId=90291 (accessed 22 July 2011).
Javier, E.L., 1997. Rice ecosystems and varieties. In: H.J. Nesbitt (Editor), Rice production in Cambodia.
Cambodia-IRRI-Australia project, pp. 39-82.
Mackill, D.J., Coffman, W.R. and Garrity, D.P., 1996. Rainfed lowland rice improvement. International Rice
Research Institute, Manila, Philippines, 242 pp.
MAFF (Ministry of Agriculture, Forestry and Fisheries) 2006. Agriculture, Forestry and Fisheries statistic in
Cambodia 2005-2006. [Online]. Available at http://faorapapcas.org/cambodia/AgriStat-Cambodia2005/
index.htm (accessed on 15 Jan 2011)
Mekong River Commission (MRC). 2010a. Assessment of basin-wide development scenarios: Technical note
10. The Mekong River Commission, Vientiane, Lao PDR. 45 pp.
Mekong River Commission (MRC). 2010b. Preliminary report on low water level conditions in the Mekong
mainstream. Technical note 10. The Mekong River Commission, Vientiane, Lao PDR. 10 pp.
Puckridge, D.W. et al., 1991. Nitrogen uptake by deepwater rice during the preflood and flooded phases, in
relation to drymatter and grain production. Field Crops Research, 27: 315-336.
Seng, L.T., Puckridge, D.W. and Thongbai, P., 1988. Cultivation of deepwater and floating rice in Kampuchea,
International Deepwater Rice Workshop. International Rice Research Institute, pp. 159-167.
Sharma, A.R. and Ghosh, A., 1998. Optimum seed rate and nitrogen fertilizer requirement of rice under semi-
deepwater ecosystem. Journal of Agronomy and Crop Science-Zeitschrift Fur Acker Und Pflanzenbau,
181: 167-172.
Singh, V.P., Hong, N.V., Sharma, A.R. and Dhanapala, M.P., 2004. Challenges and strategies in rice crop
establishment for higher productivity in flood-prone environments. In: S.I. Bhuian, M.Z. Abedin, V.P.
Singh and B. Hardy (Editors), Proceedings of the international workshop on flood-prone rice systems.
Los Banos (Philipines): International Rice Research Institute, Gazipur, Bangladesh, 9-11 January 2001,
pp. 189-204.
th
Submergence Escape in Oryza glaberrima Steud.

Jun-Ichi Sakagami
a,
*, Chiharu Sone
a
, Naoyoshi Kawano
b

a
Crop, Livestock and Environment Division, Japan International Research Center for Agricultural Sciences,
Tsukuba, Ibaraki, Japan
b
Rural Development Division, Japan International Research Center for Agricultural Sciences,
Tsukuba, Ibaraki, Japan
*Corresponding author: Crop, Livestock and Environment Division,
Japan International Research Center for Agricultural Sciences,
1-1, Ohwashi, Tsukuba, Ibaraki 305-8686, Japan
Tel.:+81 29 838 6368; Fax: +81 29 838 6355.
[email protected]

Abstract

Oryza glaberrima, an African monocarpic annual rice derived from Oryza barthii, is grown in traditional rice
producing wetland areas of West Africa. Oryza sativa, an Asian rice that varies from annual to perennial, is
derived from Oryza rufipogon. Genotypes of O. glaberrima are inherently lower yielding than those of O. sativa
and are, therefore, cultivated in fewer areas. However, because they grow adequately in unstable environments
such as those with water stress, they appear to tolerate severe environmental stress. Cultivars of O. glaberrima
are roughly divisible into two ecotypes: upland and lowland. However, it might be that O. glaberrima is a
valuable rice species for flooding conditions in all cases. To elucidate the physiological responses of young rice
plants to short-term submergence stress, so-called flash flooding, under rainfed conditions for O. glaberrima by
comparison with several genotypes for lowland adapted, deepwater adapted shoot elongated escape and Sub1
of O. sativa, 30-day-old seedlings were submerged completely for 10 d at 45 cm water depth at 13 d after
transplantation in a lowland field. In fact, O. glaberrima showed higher shoot elongation ability during
submergence than any genotype of O. sativa that we tested. However, O. glaberrima lodged easily after the end
of submergence because of longer and more rapid shoot elongation during submergence. Therefore, it triggered
a decrease in its survival rate. On the other hand, various lines of 35 O. sativa and 27 O. glaberrima, including
some classified as short-term submergence tolerant, were compared for submergence tolerance in field and pot
experiments to long-term submergence tolerant varieties in other words, deepwater varieties. Submergence-
tolerant cultivars of O. sativa were unable to survive prolonged complete submergence for 3137 d, which
indicated that the mechanism of suppressed leaf elongation that confered increased survival of short-term
submergence was inadequate for surviving long periods underwater. The superior tolerance of deepwater O.
sativa and O. glaberrima genotypes to prolonged complete submergence appeared to be attributable to their
greater photosynthetic capacity developed by leaves that had newly emerged above the floodwater. Cultivars of
O. glaberrima adapt to long-term complete submergence. Cultivar Saligbeli adapted to short to long term
submergence.

Keywords: glaberrima, lodging, photosynthesis, shoot elongation, submergence escape

Introduction

Rice farming in Africa began approximately 3500 years ago (Porter, 1970). The rice variety
cultivated at the time was African rice (Oryza glaberrima Steud.), which is native to the continent
(Chu and Oka, 1972). African rice is well adapted to the severe local climate, but it has had little
opportunity to be improved or selected by humans. It is, therefore, regarded as wild and of low
productivity. For that reason, Asian rice (O. sativa L.) accounts for a high proportion of the rice
consumed in Africa today. However, the development and promotion of a NEw RIce for AfriCA
(NERICA) is attracting attention in Africa. Moreover, the properties of African rice, which was
employed as a parent strain in the production of NERICA, are now being reassessed. In this
manner, rice farming in Africa has been developed differently from that in Asia, and cultivation and
cooking methods also differ in many ways. Farmers cultivate rice in irrigated lowlands in Asia,
th
although rainfed uplands in Africa account for most rice fields. African farmers attach great
importance to the quantity immediately after cooking in many cases (Sakagami et al., 2008).
Although rice consumption in African countries has shown an increasing trend in recent years, the
production rate is not sufficient to meet the demand. The volume of imported rice is increasing
annually, which is having a detrimental effect on African countries economies.
In general, rice cultivation is vulnerable to natural disasters in West Africa. One reason is
the shortage of suitable irrigation systems. The area of irrigation is less than 20% of the total area of
rice cultivation, and most rice is planted in rainfed regions (Balasubramanian et al., 2007).
Therefore, rice cultivation in West Africa is strongly influenced by precipitation or overflow from
rivers. However, the status of damage to rice plants by flooding in West Africa has not been
understood well until now. Upland rice is severely influenced by rainfall because of the lack of
standing water. Yields of upland rice are very low (around 1 t ha
-1
) compared with those of lowland
rice cultivation (around 2 t ha
-1
) (Norman and Otoo, 2003). Lowlands, therefore, offer greater
potential for raising rice production, and represent about 2050 million hectares, depending on the
definition used. At present, only about 1020% of this area is under cultivation (Africa Rice Center,
2004), thereby offering great potential for rice farming expansion. However, rice plants in lowland
areas are often damaged by floods caused by heavy rain. It is, therefore, important to study the
effects of submergence on rice plants to develop sustainable rice production in West Africa.
Genotypes of O. glaberrima are inherently lower yielding than those of O. sativa and are,
therefore, cultivated in fewer areas (Linares, 2002). However, because they grow adequately in
unstable environments such as those with water stress, they appear to tolerate severe
environmental stress. Flooding imposes severe selection pressure on plants, principally because
excess water in the plant surroundings can deprive them of certain basic needs, notably of oxygen
and of carbon dioxide and light for photosynthesis. It is a major abiotic influence on species
distribution and agricultural productivity world-wide. Based on our analysis, most O. glaberrima
varieties adapt well when floods are deeper and when they entail long-term submergence in Africa
because of their greater photosynthetic capacity developed by leaves that have newly emerged
above floodwaters through rapid shoot elongation.


Experiment 1: Responses to short-term submergence flash flood
To elucidate the physiological responses of young rice plants to short-term submergence
stress, so-called flash flooding, under rainfed conditions for O. glaberrima by comparison with
several genotypes for lowland adapted, deepwater adapted shoot elongated escape and Sub1 of O.
sativa, 30-day-old seedlings were submerged completely for 10 d at 45 cm water depth at 13 d after
transplantation in a lowland field of Guinea. Dry matter production, plant height, lodging and
surviving rate were compared.

Experiment 2: Responses to long-term submergence deep water
Various lines of 35 O. sativa and 27 O. glaberrima, including some classified as short-term
submergence tolerant, were compared for submergence tolerance in field and pot experiments to
long-term submergence tolerant varieties in other words, deep-water varieties. Plants were
submerged completely for 31 d in a field experiment, and partially or completely for 37 d in a pot
experiment in a growth chamber. Dry matter production, plant height, leaf area, and photosynthetic
rate were compared.

Experiment 3: Flash flood tolerance for cultivated species
Lodging, plant height, and dry matter accumulation for 99 cultivars in O. sativa, O.
glaberrima, and interspecific hybridization progenies (IHP) were measured when 12-day-old
th
seedlings were submerged completely for 7 d in pots and in fields to make an evaluation of flash
flood tolerance.


There was a high positive correlation (P < 0.01, r =0.86) between shoot length elongation
during short term submergence and lodging score at 15 DAS (Day After Submergence) in
experiment 1. DRL (Deep-water to Rainfed Lowland genotype in O. glaberrima) showed higher
shoot elongation during submergence and a higher lodging score after desubmergence than other
genotypic groups. On the other hand, ST (Submergence Tolerance genotype) showed the opposite
features to DRL with lower shoot elongation and lodging score. RL (Rainfed Lowland genotype),
DW (Deep-Water genotype) and SE (Shoot Elongation genotype) showed intermediate traits in
shoot length elongation and lodging score between DRL and ST. Figure 1 shows the relationship
between shoot length elongation during submergence and survival rate at 19 DAS. There was a
negative correlation between shoot length elongation and survival rate (P < 0.05, r = -0.66).

Figure 1. Effect of shoot length elongation on survival rate. Survival rate was calculated for number of plants
before submergence divided by number of surviving plants at 19 day after desubmegence

ST of Sub1 showed the highest survival rate (93%) and the shortest shoot length
elongation (6.8 cm) as well as IR 62293- 2B-18-2-2-1-3-2-3 (86%, 11.5 cm) in the SE group. The
survival rate of DRL was lower compared with ST. O. glaberrima showed higher shoot elongation
ability during submergence than any genotype of O. sativa tested. However, O. glaberrima lodged
easily after desubmergence due to longer and rapid shoot elongation during submergence, and
thus triggered a decrease in its survival rate. We suggested that O. glaberrima was susceptible to
short-term submergence while it may be adapted to prolonged flooding because of improved
restoration of aerial photosynthesis and survival rate through shoot elongation ability
All cultivars of O. sativa with submergence tolerance based on the quiescence strategy
failed to regain contact with the aerial environment and died during 31 d submergence in the field
experiment 2. In contrast, all O. glaberrima genotypes resurfaced and survived submergence. The
photosynthetic rates of the youngest fully expanded leaf of the main shoot of pot-grown plants were
measured in pot experiment 2. The non-submerged rate for IR73020 (30.9 mol m
-2
s
-1
) 1
DBS(Day Before Submergence) was significantly above those for other genotypes. The rate for
Yele1A (6.74 mol m
-2
s
-1
) was the lowest. It was, however, significantly greater for Yele1A than
for other genotypes in non-submergence plots (29.2 mol m
-2
s
-1
), in partial submergence plots
(30.3 mol m
-2
s
-1
) and in complete submergence plots (34.8 mol m
-2
s
-1
) 37 DAS. The
photosynthetic rate at 37 DAS in partial and complete submergence was closely related to the NAR
(Net Assimilation Rate) during submergence in the pot experiment (Figure 2).
th

Symbols represent non-submerged plants, partially submerged plants and completely submerged plants as indicated. The
number next to each symbol indicate the cultivars: 1, Banjoulou; 2, IR71700; 3, IR73020; 4, Nylon; and 5, Yele1A

Figure 2. Relationship between net assimilation rate during submergence and photosynthetic rate after 37 d
submergence in a pot experiment.

The superior tolerance of deepwater O. sativa and O. glaberrima genotypes to prolonged
complete submergence appears to be due to their greater photosynthetic capacity developed by
leaves newly emerged above the floodwater. Vigorous upward leaf elongation during prolonged
submergence is, therefore, critical for ensuring shoot emergence from water, leaf area extension
above the water surface and a subsequent strong increase in shoot biomass. Increase in shoot
DMA after desubmergence was negatively correlated with shoot elongation during submergence, r
=0.36 (P < 0.01) in experiment 3. ST were plotted in the area of short shoot elongation and high
increase in DMA (Dry Matter Accumulation), while O. glaberrima, except for Saligbeli, were plotted
in the area opposite to that of ST. Some LS (Lowland Sativa genotype) and LI (Lowland
Interspecific progenies genotype) were plotted close to the ST for both shoot elongation and shoot
DMA. Increase in DMA after desubmergence of all US (Upland Sativa genotype) was less than that
of ST.
The first principal component explained 46.8%, and for the classification of cultivars
according to their physiological responses to flash floods. The results of the cluster analysis were
compared to the principal component analysis results (Figure 3). Principal component analysis was
performed with the increase in DMA from 1 DAD to 14 DAD, and lodging at 1 DAD, shoot
elongation during submergence, and increased DMA during submergence. In Clusters I, III, and
VIII, the main genotypes belonging to each cluster group were classified on the principal component
analysis. Cluster I, including ST cultivars, and Cluster VIII, including O. glaberrima, were positioned
in opposite regions except for Saligbeli. Saligbeli exhibited enhanced shoot elongation with the
increase in DMA during submergence. These features seemed to be a unique way to cope with
submergence.
th

Axis I is the first principal component (y =0.403942 x1 + 0.434866 x2 + 0.329416 x3 0.271996 x4). Axis II is the second
principal component (y =0.068947 x1 0.080874 x2 + 0.618871 x3 +0.722613 x4), x1, x2, x3 and x4 represent increase in
DMA after desubmergence, lodging score, shoot elongation and increase in DMA during submergence respectively. All data are
standardized. () Upland Sativa, () Lowland Sativa, () Upland Glaberrima () Lowland Glaberrima, () Upland IHP, ()
Lowland IHP, () Submergence tolerance.

Figure 3. Principal component analysis of the physiological traits linked to submergence (shoot elongation during
submergence, increase in dry matter accumulation during submergence, lodging score and increase
in dry matter accumulation after desubmergence.

References

Africa Rice Center. 2004. Going beyond the upland NERICA: another African Rice is born. In Annual Report
20032004. Cotonu, Benin.
Balasubramanian, V., Sie, M., Hijmans, RJ. & Otsuka, K. 2007. Increasing rice production in Sub-Saharan
Africa: Challenges and opportunities. Advances in Agronomy 94:55-133.
Chu, YE. & Oka, HI. 1972. The distribution and effects of genes causing F1 weakness in Oryza breviligulata and
O. glaberrima. Genetics 70:163-173.
Linares, O.F. (2002). African rice (Oryza glaberrima): history and future. Proceedings of the National Academy
of Sciences of the United States of America, 99:1636016365.
Norman, JC. & Otoo, E. 2003. Rice development strategies for food security in Africa In: Proceedings of the 20th
Session of the International Rice Commission. Food and Agricultural Organization of the United Nations.
Porteres, R. 1970. Primary cradles of agriculture in the Africa continent. In: Fage, J., Oliver, R. (eds.). African
Prehistory. Cambridge University Press, Cambridge, UK, pp. 43-58.
Sakagami, J-I., Hatta, T., Kamidozono, A., Masunaga, T., Umemoto, T. & Uchida, S. 2008. The actual condition
of traditional rice culture in inland valley delta of Niger River. JIRCAS Working Report. In: Sakagami, J-I.
Ito, O.(eds). pp. 37-52.

I
th
Toposequnential Variation in Soil Fertility and Limiting Nutrient for Rice
Growth in the White Volta Floodplain of Northern Ghana

Yasuhiro Tsujimoto
a*
, Yukiyo Yamamoto
a
, Keiichi Hayashi
a
, Alhassan I. Zakaria
b
,
Yahaya Inusah
b
, Tamao Hatta
a
, Mathias Fosu
b
, Jun-Ichi Sakagami
a

a
Japan International Research Center for Agricultural Sciences, Japan
b
Savanna Agricultural Research Institute, Council for Scientific and Industrial Research, Ghana
*Corresponding author: Japan International Research Center for Agricultural Sciences,
1-1 Ohwashi Tsukuba, Ibaraki 305-8686, Japan
Tel.: +81 29 838 6368; fax: +81 29 838 6355.
[email protected]

Abstract

Integrated floodplain resource management for rice cultivation is imperative to satisfy the growing demand of
rice in West Africa. Irrigated pot experiments were conducted with different fertilizer treatments to identify
toposequential variation in soil fertility and limiting nutrient for rice growth within the White Volta floodplains in
Ghana. Eighteen experimental soils were examined across a riverside to upland gradient, ranging from 898 to
4200 m in distance from the main riverside, from 73 to 106 m in elevation, and from 0.7 to 2338.1 m in distance
from water sources. The soil analysis revealed close correlation between N-mineralization rates and carbon
contents of the soils, which were exponentially decayed with distance from water sources. In the non-fertilized
treatments, plant N uptakes at maturity also decreased along the same transect from the water sources.
However, the dry matter production was little relevant to this toposequential factor. Various fertilizer treatments
identified remarkable effect of sulfur on rice growth, which was more significant on soils closer to waster
sources. NPK application without S increased only N concentration and N: S ratio in plant tissues but not
biomass production. The results indicated that sulfur is the primary limiting element for rice growth, and its
supplementation would be more beneficial as closer to water sources so as to effectively utilize greater N-
supplying capacity of this agro-environmental soils.

Keywords: rice, sulfur deficiency, floodplain, soil carbon, water source

Introduction

River floodplains, consisting of wide and flat plain of alluvium bordering rivers, are
expected to support a large expansion in rice cultivation area and production in Africa, of which the
major share is currently unexploited. Major constraints to expand agricultural activities into river
floodplains include difficulty in water control, risk of complete submergence of plants, occurrence of
water-borne diseases, and disadvantage in access to the road and market (Balasubramanian et al.
2007). On the other hand, this geographical environment can provide water resources as well as
relatively fertile alluvial soils compared to uplands (Buri et al. 1999). Moreover, the use of river
floodplains for rice cultivation should not cause spatial competition with the other crops due to the
risk of periodic flooding.
In the traditional lowlands in Asia, large variance in cultivation conditions and rice
productivity are commonly recognized within relatively small areas, and farmers management
practices are adapted to this variance according to the sequential changes in soil fertility and water
availability (Fukai et al. 1998). However, either quantitative data or farmers practical adoption on
the toposeqential distribution of environmental resources are scarce for rice cultivation within river
floodplains in West Africa.
Primary objectives of this study were, therefore (1) to quantify the rice productivity of soils
in relation to small-scale toposequence and (2) to identify deficient nutrient for rice growth, which
th
results can help effective use of soil nutrient resources and development of toposequence-specific
fertilizer management practices within a target environment. To achieve these objectives,
phytometry experiments with rice were conducted under various fertilizer treatments by using
multiple soils collected within a Whiter Volta floodplain in the northern Ghana. In addition to the
major macronutrients of N, P and K, target nutrients included Zn, Si and S which deficiency have
been previously reported in the region and in the similar hydromorphic soils in the other parts of the
sub-Sahara Africa (Buri et al. 2000; Tsujimoto et al. 2010).


Sampling of experimental soils
Experimental soils were collected from the top 0-15 cm at 18 points across a riverside to
upland gradient in the White Volta floodplains of northern Ghana at the beginning of rainy season in
June, 2010. The sampling points ranged from 898.7 to 4200.0 m in distance from the main Volta
riverside, from 73 to 106 m in elevation (ASTER-GDEM), and from 0.7 to 2338.1 m in distance from
water sources. The average slope angle was 0.86 % between the closest and furthest sampling
points from the riverside. Distance from water sources were calculated after extracting rivers and
back-swamps by the image analysis of Quickbird imagery. Experimental soils were air-dried for a
week in a screen house at the Savanna Agricultural Research Institute (9 26 N, 0 59 W, 183 m
asl.). Thereafter, the soils at the air-dry equivalent weight (4.2 kg) were put into 7-l plastic pots
followed by flooding and puddling with different fertilizer treatments.
The chemical and physical properties of the experimental soils were analyzed after air-
dried and sieved. Total C and N were determined by automatic high sensitive NC analyzer,
Sumigraph NC-220F (SCAS, Japan). Mineralizable nitrogen was determined by a 4-week anaerobic
incubation at 30C as the amount of NH
4
+
-N extracted with 10% KCl solution. Available phosphorus
content was measured by Bray No.2 method. Extractable sulfate was determined by extraction with
KH
2
PO
4
solution containing 500 mg l
-1
P. CEC was measured by the ammonium acetate extract
method at pH 7.0. Exchangeable bases were determined by plant atomic emission spectrometer,
ICPE-9000 (Shimadzu, Japan). Soil texture was determined by sieving and pipetting method.

Experiment design and measurements
Two pot experiments were conducted. In the Experiment 1, rice was grown with no
fertilizer inputs, using all the 18 experimental soils. In the Experiment 2, three of the 18
experimental soils were selected in a wide range of the distance from water sources (Bottom: 40 m;
Middle: 501 m; Top: 1870 m), for which ten different fertilizer treatments were established including
no fertilizer treatment in the Experiment 1: 1. Control (no fertilizer); 2. +N; 3. +P, 4. +K, 5. +NP; 6.
+NK; 7. +NPK, 8. +NPKSi, 9. +NPKZn, 10. +NPKS. The chemical forms and application rates for
each nutrient were 0.70 g N, 0.22 g P, 0.36 g K, 1.87 g Si, 0.05 g Zn, and 0.23 g S per pot as Urea,
NaH
2
PO
4
, KCl, SiO
2
, ZnCl
2
, and Na
2
SO
4
, respectively. Both experiments had three replicates,
followed by the same cultivation management and measurements. Two 21-day old seedlings of a
local cultivar, Jasmine85, were transplanted at a rate of one hill per pot on June 26 in 2010, and
were subsequently harvested on October 8 in 2010. The water level was kept above 2 cm
throughout the rice growing period. Weeds were removed manually. No specific pest management
was conducted.
The plants were harvested from each pot at maturity. The dry weights of the plant samples
were determined after oven drying at 80C to a constant weight. The plant N concentration was
determined by using automatic high sensitive NC analyzer, Sumigraph NC-220F (SCAS, Japan).
The plant nutrient concentrations of P, K, S, Mg, Ca, Zn, Fe, Mn, Cu, and B were analyzed by plant
atomic emission spectrometer, ICPE-9000 (Shimadzu, Japan), after digesting each sample with
HNO
3
and H
2
O
2
in microwave digestion system (MLS-1200 MEGA, Milestone Inc.). The plant
th
nutrient uptakes were calculated as the product of the dry weight and the nutrient concentration of
each plant tissue. Statistic analysis was performed by using JMP 8 software (SAS Institute Inc.).


Toposequential variation in soil fertility and plant growth (Experiment 1)
The results of soil analysis revealed large variances in soil properties within the gently
sloping floodplain area (Table 1). The total carbon (TC) and total nitrogen (TN) contents ranged
from 3.48 to 30.15 g kg
-1
and from 0.28 to 2.25 g kg
-1
, respectively. Although differing among the
locations, available P and extractable S were both below the critical deficiency levels shown by
Dobermann and Fairhurst (2000). This was in accordance with the previous studies conducted in
the same agro-ecological zones of West Africa (Buri et al. 1999, 2000).

Table 1. Soil properties and its correlation with the total carbon contents (n=18).

pH 1:2.5 (H
2
O) 6.29 7.56 5.42 10.8 -0.43
Clay (%) 13.65 30.96 5.60 54.2 0.80***
Total C (g kg
-1
)
11.91 30.15 3.48 64.4 -
Total N (g kg
-1
)
0.89 2.25 0.28 65.3 0.91***
Mineralizable N (mg kg
-1
)
43.53 141.10 1.42 104.5 0.96***
Available P (mg kg
-1
)
11.26 31.85 1.98 79.5 0.58*
Extractable S (mg kg
-1
)
8.72 14.48 6.09 24.4 0.50*
CEC (cmol kg
-1
)
6.97 15.10 3.07 56.8 0.80***
Exchangeable cation (cmol kg
-1
)
Na 0.75 1.54 0.33 50.3 0.57*
K 0.35 0.47 0.24 23.3 0.64**
Mg 1.05 2.65 0.40 68.9 0.80***
Ca 1.89 4.21 0.80 59.6 0.78***
Mean Max Min
coefficiency
of variation
(%)
correlation
coefficient to
Total C

The total carbon (TC) contents of the soils correlated to most of the other soil properties,
exponentially decreased as the distance from water sources (Figure 1a). This toposequential
gradient in the TC, SOC or clay contents of the soils was also observed in the other rice-growing
lowlands of Asia (Homma et al. 2003; Tsubo et al. 2006). The accumulated TC contents in the lower
parts of the toposequence were most likely attributable to greater deposition of clay minerals, and to
longer periods of submergence that alleviates the decomposition of organic substrates (Sahrawat
2004).
The total N uptakes of rice plants also showed exponential reduction along the same
transect from the water sources (Figure 1b). This could be explained by large differences in soil
mineralizable N, that were highly correlated with the TC contents (Table 2). Soil mineralizable N
was regarded as a good index of soil N-supplying capacity, and sufficiently correlated with plant N
uptakes under non-N fertilized conditions in previous studies (Russell et al. 2006; Tsujimoto et al.
2010). However, top dry matter (TDM) yield was less relevant to this toposequential factor (Figure
1b). The TDM production highly fluctuated within a 100 m radius of water sources, and one had a
relatively high yield level at upper area of the floodplain. This discrepancy in responses with rice
production to N-supplying capacity of the soils indicated that there existed other limiting elements
apart from N.
th

r = 0.54***
0
10
20
30
40
50
0
0.1
0.2
0.3
0.4
0.5
0 500 1000 1500 2000 2500
D
r
y

m
a
t
t
e
r

y
i
e
l
d

(
g

p
o
t
-
1
)
P
l
a
n
t

N

u
p
t
a
k
e
s

(
g

p
o
t
-
1
)
Distance from water sources (m)

r = 0.68***
0
5
10
15
20
25
30
35
0 500 1000 1500 2000 2500 S
o
i
l

t
o
t
a
l

C

c
o
n
t
e
n
t
s

(
g

k
g
-
1
)
Distance from water sources (m)

Figure1. Relationship between distance from water sources and (a) soil TC contents and (b) plant N uptakes
(closed circles: ) and top dry matter yield (cross marks: X).

Effects of fertilizer treatment and soil type on rice growth (Experiment 2)
The results of ANOVA showed significant F-values for the main and interactive effects of
fertilizer treatment and soil type on the TDM production. The application of NPKS demonstrated
stunningly higher TDM yields compared to the Control plots (Table 2). The differences in TDM
yields between NPKS and Control plots were greater as closer to water sources (80.5; 40.7; and
29.7 g pot
-1
on the Bottom, Middle, and Top soils, respectively). On the other hand, the application
of N, P, and K or combinations of these elements without S showed no effects on the TDM yields
for any of the experimental soils.

Table 2. Top dry matter yields and N: S concentration ratio at maturity as affected by different fertilizer
treatments for the three experimental soils.

Bottom Middle Top Bottom Middle Top
C
14.7
fghijkl#
23.5
def
12.7
hijkl
29.2
f
13.0
hi
12.9
hi
N
12.4
ghijklm
27.0
d
10.1
jklm
51.6
ab
25.4
fgh
47.9
ab
P
14.6
fghijkl
22.2
defg
12.8
hijkl
27.8
fg
11.3
i
14.7
ghi
K
18.6
defghij
17.1
defghijk
11.5
hijklm
26.9
fgh
12.5
hi
14.9
ghi
NP
10.7
ijklm
24.5
def
9.3
ijklm
45.0
abcd
31.6
ef
50.4
ab
NK
14.6
fghijkl
20.3
defgh
7.9
klm
57.1
a
34.0
cdef
50.8
ab
NPK
16.5
fghijkl
16.5
efghijk
5.9
lm
51.8
ab
43.8
bcde
47.1
abc
NPKSi
18.9
defghij
25.2
de
12.0
hijklm
49.6
ab
33.6
def
48.3
ab
NPKZn
19.5
defghi
12.0
hijklm
3.2
m
33.7
def
44.6
abcde
56.5
ab
NPKS
95.2
a
71.2
b
42.4
c
13.4
hi
6.6
i
7.1
i
df df
Soil type (S) 2 2
Fertilizer (F) 9 9
S x F 18 18
F-values F-values
11.1***
319.2***
24.4***
N: S ratio
#Values within the next three columns followed by the same letter do not differ significantly at
P<0.05 by Tukey's HSD multiple range test. ***Significant at P<0.001.
98.7***
159.8***
Fertilizer
Top dry matter yield (g pot
-1
)
166.1***

The high N: S ratio, notably on the bottom soil, and the increased values by the N
application without S also implies the unbalanced supplies between N and S (Table 2). The ratios
(a)
(b)
th
reduced only by adding S as a result of the substantial increases in biomass production. In a
conventional study, Yoshida and Chaudhry (1979) suggested a critical N: S ratio for S deficiency at
14 in straw, and they demonstrated 50% of biomass reduction at the value of 40. The other study
also indicated the similar value as a critical N: S ratio, and slightly higher value for grains (Islam and
Ponnamperuma, 1982). Our results indicated that sulfur shortage severely hampers rice growth as
well as maximum efficiency of N from either inherent soils or fertilizers in the target floodplain. The
limiting S supply was also apparent in the S concentration values, that were all below the critical
deficiency level at 0.06% (Dobermann and Fairhurst, 2000), among the rice plants in the
Experiment 1. The other macro- and micro- nutrient concentration values were above the critical
deficiency level except four of the 18 plots for the P level (data not shown).

Conclusions

This study revealed steep gradients in soil fertility within a gentle slope of a river floodplain
in the northern Ghana. The phytometrical experiments suggested that the spatial variances in soil
fertility for rice growth were mainly represented by the N- and S- supplying capacity of the soils.
Once the limit of S is lifted, rice production is expected higher as closer to water sources due to
exponentially greater amounts of N-supplying capacity of the soils. A further study requires
identifying spatial distributions in S-supplying capacity of the soils, so that efficient fertilizer
management practices can be developed on a basis of balancing N and S applications. The
development of toposequence-specific fertilizer management will certainly help effective extension
of rice production within the target floodplain environments.

References

Balasubramanian V, M Sie, RJ Hijmans, K Otsuka, 2007. Increasing rice production in sub-saharan Africa:
Challenges and opportunities. Adv. Agr. 94, 55-133.
Buri MM, T Masunaga, F Ishida, D Kubota, and T Wakatsuki, 1999. Soils of flood plains in West Africa: general
fertility status. Soil Sci. Plant Nutr. 45(1), 37-50.
Buri MM, T Masunaga, and T Wakatsuki, 2000. Sulfur and zinc levels as limiting factors to rice production in
West Africa lowlands. Geoderma 94, 23-42.
Dobermann A, and TH Fairhurst, 2000. Rice: Nutrient disorders and nutrient management. International Rice
Research Institute (IRRI), Los Banos, Philippines.
Fukai S, P Sittisuang, and M Chanphengsay, 1998. Increasing production of rainfed lowland rice in drought
prone environments-A case study in Thailand and Laos. Plant Prod. Sci. 1(1), 75-82.
Homma K, T Horie, T Shiraiwa, N Supapoj, N Matsumoto, N Kabaki, 2003. Toposequential variation in soil
fertility and rice productivity of rainfed lowland paddy fields in mini-watershed (Nong) in Northeast Thailand.
Plant Prod. Sci. 6(2), 147-153.
Islam MM and FN Ponnamperuma, 1982. Soil and plant tests for available sulfur in wetland rice soils. Plant Soil
68, 97-113.
Russell CA, BW Dunn, GD Batten, RL Williams, JF Angus, 2006. Soil tests to predict optimum fertilizer nitrogen
rate for rice. Field Crops Res. 97, 286301.
Sahrawat KL, 2004. Organic matter accumulation in submerged soils. Adv Agr. 81, 169-201.
Tsubo M, J Basnayake, S Fukai, V Sihathep, P Siyavong, Sipaseuth, M Chanphengsay, 2006. Toposequential
effects on water balance and productivity in rainfed lowland rice ecosystems in Southern Laos. Field Crops
Res. 97, 209-220.
Tsujimoto Y, K Homma, and T Shiraiwa, 2010. The effects of soil drying and rewetting on rice growth in lowland
aquatic Ferralsols in the southeastern forest region of Madagascar. Plant Soil 333, 219-232.
Yoshida S and MR Chaudhry, 1979. Sulfur nutrition of rice. Soil Sci. Plant Nutr. 25 (1), 121-134.

th
Varietal Differences of Rice (Oryza sativa L.) Genotypes for Aleurone Traits
Contributing to Lipid Content

Ohn Mar Khin
a
, Masao Sato
b
, Tong Li-Tao
a
, Yuji Matsue
b
, Atsushi Yoshimura
b
, Toshihiro
Mochizuki
b*

a
Graduate school of Bioresource and Bioenvironmental sciences, Kyushu University, Fukuoka, Japan
b
Faculty of Agriculture, Kyushu University, Fukuoka, Japan
*Corresponding author: Experimental Farm, Kyushu University, Harumachi 111,
Kasuya-machi, Kasuya-gun, Fukuoka 811-2307, Japan
Tel.:+81 92 612 2865; Fax: + 81 92 612 2865.
[email protected]

Abstract

The increasing demand for oil is more than the increasing production of oil seed crops. Rice bran oil has been
used extensively in Japan, Korea, China, Taiwan, Thailand and Pakistan. Interest in rice oil is increasing
because it is identified as healthy oil that reduces serum cholesterol. In rice seed, the lipid content deposited in
the aleurone layer and embryo has been reported from 17.5 to 21.7%. To explore the useful genetic resources
for aleurone traits closely related to the lipid content, 333 varieties were investigated. Brown rice seeds were cut
in cross around center with razor blade and the outermost region of the cut surface stained with oil red O were
measured with a fluorescence microscope. As a result, there were wide variations in stained area among
varieties and many varieties with large stained area were found in Japonica group. Twenty varieties were
selected according to their stained area to cover the whole range among varieties used and confirmed their
thickness of aleurone layer by using micro thin section that was made by Leica cryostat with slight modification
of the Kawamotos film method (2008). The photos of sections were taken under a light microscope. The
aleurone traits were measured by using Image J software. The amount and content of triacylglycerol (TAG) of
brown rice without embryo were also measured. Both amount and content of TAG were significantly correlated
with the area, the average thickness and the percentage of aleurone layer. These results suggest that the
aleurone traits will be able to use as good indicators for selection of rice varieties with high TAG amount and
content.

Keywords: aleurone layer, lipid content, rice bran oil, triacylglycerol, varietal differences.

Introduction

Rice (Oryza sativa L.) is one of the world's most important food crops, primarily in East and
Southeast Asia. Rice bran is a valuable by-product of rice milling that contains a high concentration
of nutritional compounds including edible lipids. Rice bran oil is used in foods, feed and industrial
applications. More recent efforts have emphasized the nutritional benefits of rice bran oil. It can
aptly be concluded that rice bran oil is an important future source for edible and essential oils in all
over the world.
Rice bran oil has been extensively used in Asian countries such as Japan, Korea, China,
Taiwan, Thailand and Pakistan (Kahlon, et al., 1992). The use of rice bran oil in Japan, where it is
the largest volume domestically produces vegetable oil, is as a frying oil (Orthoefer, 2005). In brown
rice, the lipid content is from 2.3 to 3.9% (Juliano, 1977, Fujino, 1978). Embryos and aleurone
layers in rice are major tissues to deposit lipids and the content in these tissues has been reported
from 17.5 to 21.7%. The content in rice embryos and aleurone layers is equivalent to that of
soybean and cotton seeds. The physiological role played by the aleurone layer is to provide a
reserve site for minerals to deposit, which are crucial as an essential nutrient when seeds germinate
th
Tanaka et al., 1973). In the cells, oil bodies and aleurone particles are most predominant and seem
to play a more important physiological function than starchy endosperm.
Because rice is primarily used for food, starchy endosperm or milled rice is more important.
Little effort has been made to study about rice bran layer. There is some information about the
thickness of aleurone layer of some varieties. Genes for enlargement of embryos and aleurone
layers can contribute to an increase in the oil content of rice grains (Omura and Satoh, 1981). For
such reason, characterization of genetically broad rice germplasms for thickness of aleurone layer
is of special importance in identifying potential varieties. Therefore, the objectives of this study were
to evaluate the thickness of aleurone layer and to compare it with the storage lipid of the seed.


Halfseed staining method
All experiments were conducted at Kyushu University in 2010-2011. Three hundred and
thirty three rice varieties including 176 of IRRI Core Collection, 59 of World Rice Collection and 96
of Core Collection stored at Kyushu Uniersity, were used. The brown kernels were cut in half
around center with razor blade and then stained with oil red O for 5 -10 minutes and then rinsed
well in 70% ethanol for 3 - 4 times. The total cut surface area and the area of the stained region
were measured by using a fluorescence microscope (BZ 9000, Keyence Co. Ltd Osaka,Japan).
Then the percentage of the stained area and the average thickness of the stained region can be
calculated by using the following formula.
the area of the stained region (m
2
)
The percentage of the stained area (%) = x 100
the total cut surface area (m
2
)

the area of the stained region (m
2
)
The average thickness of the stained region (m) =
the circumference (m)

Sectioning method
To confirm that the relationship between the thickness of the stained region and the real
thickness of the aleurone layer, we selected 20 varieties according to their stained area to cover the
whole range among varieties tested. The measurements were made by using micro thin section that
was made by Leica cryostat with slight modification of the method of Kawamoto (2009). The
sections were stained with Hematoxylin and Eosin and examined under a light microscope. The
aleurone traits were measured using Image J software. Then the percentage of the aleurone layer
and the average thickness of aleurone layer were calculated by the same formulae in half-seed
staining method.

Measurement of Triacylglycerol (TAG)
The storage lipids (triacylglycerol: TAG) of selected varieties were analyzed. Hundred
brown kernels without embryos were milled (Degree of milling: 90%) in a mall-scale rice mill. The
lipids were extracted from the rice bran by the method of Folch et al. (1957). The TAG content was
measured using enzyme assay kits (Triglyceride E test; Wako Pure Chemicals Osaka, Japan).


In each trait, the varieties were significantly different. Varietal groups were also
significantly different in all traits except in percentage of stained area. Most of the indica varieties
have smaller cut surface area. The smallest one was found in wild rice and the largest one in
th
tropical japonica. The mean of total cut surface area was 4.01 mm
2
. There was wide variation from
0.07 to 0.35 mm
2
for area of the stained region and the mean was 0.18 mm
2
. There were many
varieties with large stained area in japonica group (Figure1). The smallest stained area was found in
wild rice. Some varieties with large stained area were also found in indica, intermediate hybrid and
tropical japonica. Although the percentage of stained area (%) was significantly different among
varieties, the varietal groups were not significant and the mean was 4.45 %. In japonica group,
many varieties with large thickness of stained region were found (Figure1). But there were also
some indica varieties with large thickness of stained region. The mean of the thickness of stained
region was 20.15m. The results revealed that the varieties with smallest ones were found in indica
and wild groups.

indica japonica Tropical japonica Intermediate hybrid Wild

Figure 1. Frequency distribution of aleurone traits of different varietal groups.

indicates the selected varieties to check the aleurone layer, *** indicates the significance at 0.001 level.

Figure 2. The relationship between the stained area (mm
2
) and total cut surface area (mm
2
) of 333 rice varieties.

We selected 20 varieties according to their value of stained area to cover the whole range
of varieties tested (Figure 2). The total cut surface area was nearly the same in half seed staining
method and sectioning (Table.1). The mean of aleurone area was 0.27 mm
2
and the range was
0.12 - 0.42 mm
2
(Table 1). It was larger than the area of stained region. This may be due to the fact
GEMJYA
JYANAM
YELAIK MEEDON
PTB25
PAI-KAN-TAO
PAKHE DHAN
MARAYA1
AICHI ASAHI
FUKUHIBIKI
KINMAZE
KOSHIHIKARI
LO1050
LO1050
Mizuhochikara
NIPPONBARE
TA HUNG KU
TAICHUNG 65
IR24
IR64
KHAO KAP
XANG
MA HAE
TAL 214
y = 14.956x + 1.3617
2
2.5
3
3.5
4
4.5
5
5.5
6
6.5
0.05 0.1 0.15 0.2 0.25 0.3 0.35
T
o
t
a
l

c
u
t

s
u
r
f
a
c
e

a
r
e
a

(
m
m
2
)
Stained area (mm
2
)
r= 0.78
th
that the stained region may become thinner than the real one depending on the time taken to wash
the seed in 70% ethanol after staining. The correlation between these two parameters was
significantly high (r=0.81***) (Figure 3). We can, therefore, use the area of stained region as a good
indicator for selecting varieties for thickness of aleurone layer. The range of the thickness of
aleurone layer was 22.88 - 48.78 m (Table 1). The thickness of aleurone layer was larger than and
significantly correlated with that of stained region (r=0.59**, data not shown). The percentage of
aleurone layer was higher than that of the area of stained region and the correlation between these
two parameters was not significant (r=0.24, data not shown).

*** indicates significance at 0.001 level.

Figure.3. The relationship between the stained area (mm
2
) and the aleurone area (mm
2
) of 20 rice varieties.

Table 1. Mean with the standard deviation of aleurone traits and Triacylglycerol (TAG) content of 20 rice
varieties

Sectioning method Half-seed staining method

Total cut surface area (mm
2
)

4.19 0.99
(1.93 - 5.60)

4.24 0.86
(1.97 - 6.00)
Aleurone area (mm
2
)
0.27 0.07
(0.12 - 0.42)

0.18 0.05
(0.07 - 0.32)
Percentage of aleurone area (%)
6.45 0.95
(0.20 - 9.00)

4.14 0.83
(2.30 - 6.49)
Thickness of aleurone layer (mm)
35.26 6.12
(22.88 - 48.78)

19.23 4.28
(10.00 - 29.14)
Amount of TAG (mg) in 100 seed
18.78 7.91
(6.89 - 41.1)

Content of TAG (mg /g of seed)
8.19 2.3
(5.02 - 14.72)

The values in parentheses indicate the range of each parameter.

The amount of TAG increased with increasing aleurone area. The range of amount of TAG
without embryo in 100 brown seed ranged from 6.89 to 41.1 mg among 20 varieties tested. It was
highly correlated with the area (r=0.71***) and thickness of aleurone layer (r=0.67**) (Figure 4).
However, the percentage of aleurone area was not correlated with the amount of TAG. The content
of TAG also increased with increasing the aleurone area. The range of content of TAG without
embryo in 1g of brown kernel was from 5.02 to 14.72 mg/g among 20 varieties tested. It was highly
th
correlated with the area (r=0.61**), percentage (r=0.58**) and average thickness of aleurone layer
(r=0.68**) (Figure 4).

** and *** indicate significant level at 0.01 and 0.001 respectively.

Figure 4. Relationship between TAG and aleurone traits of 20 rice varieties.

Conclusions

There was wide variation in aleurone traits among the genetically diverse rice varieties.
The correlation between the aleurone area by sectioning method and the stained area by half-seed
staining method was significantly high. Therefore, thestained area could be used as a good
indicator for selecting varieties for thickness of aleurone layer. Furthermore, there were high
correlation between aleurone area and aleurone thickness, and TAG. So, selection of varieties with
high lipid content could be done without measuring directly lipid content of the varieties. A great
potential was obtained to produce rice bran oil and it did not require any special cultivation since it is
a by-product of the rice milling process.

References

Fujino,Y. 1978. Rice lipids. Cereal Chem. 55: 559 - 571.
Juliano, B.O.1977. Rice lipid, IRRI. Los Banos,Phillippines: 21pp.
Kahlon T et al., 1992. Cereal Chem. 69: 485 - 489.
Kawamoto.T. 2009. Kawamotos Film method 2008. Medical Technology. 72: 76 - 83.
Omura, T. and H. satoh. 1981. Possibility of chemical breeding in rice. Current Advances in breeding
(Ikushugaku saikan no shinpo) 22:10 -19. (J)
Orthoefer F.T. 2005. Rice Bran Oil. In Baileys Industrial Oil and Fat Products, 6
th
Edition, volume 6. John Wiley
& Sons, Inc., Hoboken, New Jersey. Pp 465 - 489.
TanakaK, T Yoshida, K Asada and Z Kasai. 1973. Subcellular particles isolated from aleurone layer of rice
seeds. Arch. Biochem. Biophys. 155: 136 -143.

th
Development of New Cytoplasmic Male Sterile Lines with
Good Flowering Behavior for Hybrid Rice Breeding

Indrastuti A Rumanti
a
, Bambang S Purwoko
b*
, Iswari S Dewi
c
, H Aswidinnoor
b

a
Indonesian Center for Rice Research, Ph.D. Student at Graduate School, Bogor Agricultural University
b
Department of Agronomy and Horticulture, Faculty of Agriculture, Bogor Agricultural University
c
Indonesian Center of Agricultural Biotechnology and Genetic Resources Research and Development
*Corresponding author: Jalan Meranti, Darmaga, Bogor 16680 Indonesia.
Tel.: +62 251 8629353.
[email protected]

Abstract

Intensive use of single source of male sterile cytoplasm (i.e. wild abortive or WA) in developing hybrid rice might
lead to genetic vulnerability associated with susceptibility to pests and diseases. The research aim was to
develop new cytoplasmic genetic male sterile lines (CMS) from 3 different cytoplasmic sources (WA, Gambiaca
and Kalinga). Anther culture and successive backcrosses were conducted to develop new CMS. The screening
of bacterial leaf blight to each CMS was done through artificial inoculation using three isolates i.e. pathotype III,
IV and VIII. The results showed that combination of anther culture and backcrosses obtained 6 CMS lines of WA
type, 3 CMS lines of Kalinga type, and 1 CMS line of Gambiaca type. The lines showed complete and stable
sterility from first to fifth backcross generations. Some of them also showed resistance to certain Xanthomonas
oryzae pathotypes. The new CMS lines with WA, Kalinga and Gambiaca cytoplasm were early in maturity with
flowering behavior better than IR58025A (check CMS), such as larger stigma, higher stigma exertion, wider
angle and longer duration of glume opening during anthesis. The accumulation of good flowering behavior
increased seed set of the new CMS lines yielded from outcrossings. It ranged from 4.7525.9%, meanwhile
IR58025A seed set only reached 2.98%. Corellation analysis showed high positive and significant value
between seed set of the new CMS lines and stigma width (r = 0.44*), stigma exertion (r = 0.54*) and angle of
glume opening during anthesis (r = 0.42*), respectively. The seed set was also affected by some flower
characters of the maintainer lines such as filament length and angle of glume opening during anthesis. The
results indicated that the new CMS lines with diferent cytoplasm sources could be used in hybrid rice breeding.

Keywords: rice, cytoplasmic male sterility, flowering behavior, resistance, bacterial leaf blight

Introduction

Hybrid rice is able to increase rice productivity about 15-20% higher than the best
commercial inbred varieties. Currently, hybrid rice technology is used in a large scale cultivation in
several Asian countries. Hybrid rice covers more than 50% of rice total area in China (You et al.,
2006). Three line system is generally used in Indonesia. This system needs three parental lines:
cytoplasmic male sterile line (CMS/A line), maintainer line (B line) and restorer line (R line). Hybrid
is the first filial generation of a cross between cytoplasmic male sterile line as female parent and
restorer lines as male parent. The hybrid often exhibits heterosis or hybrid vigor, where hybrid
progeny shows superior growth characteristics relative to one of the parental lines (Eckards, 2006).
The commercial hybrid refers to a superior F
1
, which not only performs better than its parents but
also shows significant yield superiority over the best high yielding inbred variety of similar growth
duration (Virmani & Kumar, 2004). Based on those, superior parental lines i.e. CMS needs to be
developed.
CMS as female parent is a key factor for hybrid rice breeding. CMS is a condition under
which a plant is unable to produce functional pollen (Eckardt, 2006). This line provides a valuable
tool in production of hybrid seed in self-pollinating crop species including rice. Development of CMS
in three line systems of hybrid rice breeding faces problems among others instability of pollen
th
sterility, flower behaviour not fully supporting outcrossing rate, and susceptibility to pests and
diseases. Unstable pollen sterility causes difficulty in achieving high heterosis of the hybrid rice and
its seed production. The low seed yield has been implicated in higher price of the hybrid seed. Wild
Abortive (WA) CMS is mainly used in hybrid rice breeding in Indonesia (Suwarno et al., 2003) and
elsewhere. This might lead to genetic vulnerability associated with susceptibility to pests and
diseases (Li et al., 2007). Therefore, breeding of new CMS having stable pollen sterility derived
from diverse cytoplasm sources and resistant to pests and diseases are warranted.
Commercial CMS should have good outcrossing rate, complete and stable sterile pollen,
easy restorability, good and wide combining ability with any restorer lines, short plant, good
exsertion of panicle, more than 70% of stigma exsertion, good quality, resistant to pests and
diseases and adapted to target environment (Yuan et al., 2003). Dewi et al. (2007) identified 19
doubled haploid of maintainer line candidates through anther culture from F
1
of crossing between
introduced CMS and donor lines resistant to bacterial leaf blight. The doubled haploid lines are
potential maintainers to be converted to CMS because these lines were homozigous and having
male sterile gene with normal cytoplasm. Rumanti et al. (2009) tested 48 F
1
s, derived from testcross
between cytoplasmic male sterile sources with those doubled-haploid maintainer lines, and 14 F
1
s
were completely sterile (100 % pollen sterility). The objectives of this research were to develop
stable and completely sterile CMS lines from three different cytoplasmic sources, to evaluate
resistance of the new CMS to bacterial leaf blight and study of flower behavior of the new CMS that
support outcrossing ability.


Development of cytoplasmic male sterile lines through succesive backcross
Genetic material in this research were backcross population (F
1
BC
n
) between CMS
candidates with their maintainer doubled haploid lines. CMS from International Rice Research
Institute (IRRI) were used as cytoplasm donors, i.e. 3 CMS of wild abortive type (IR58025A,
IR62829A, dan IR68897A), one Gambiaca type (IR80154A) and one Kalinga type (IR80156A).
Succesive backcrosses were done 5 times. Each CMS candidate or female parent (F
1
BC
n
) was
planted in 2 rows with 12 plants each, while male parent or their maintainer were planted in 3 rows
with 12 plants each. Flowering syncronization was achieved by staggered planting of male parents
in a 3-day intervals. Selection was based on pollen sterility in each F
1
BC
n
. Observation were done
on each F
1
BC
n
generation for pollen sterility (%) (IRRI, 2002).

Resistance evaluation of the new cytoplamic male sterile lines to bacterial leaf blight
Ten new CMS were planted in the field in 2 rows with spacing of 20 x 20 cm. Plants were
inoculated with 10
8
cfu concentration of Xanthomonas oryzae pathotype using artificial method (leaf
cutting/clipping). Disease severity was observed following modified IRRI method (IRRI, 2002) when
susceptible check achieved 90% severity. Score of disease severity is shown in Table 1.

Table 1. Score of disease severity

Scale Ratio of lesio length and leaf length (%) Reaction
1 1-5 R (Resistant)
3 >5-12 MR (Moderate Resistant)
5 >12-25 MS (Moderate Susceptible)
7 >25-50 S (Susceptible)
9 >50-100 VS (Very Susceptible)

th
Evaluation of flowering behaviour which supports outcrossing ability between new CMS and
their maintainer
Five new CMS lines (BI485A, BI599A, BI619A, BI639A dan BI665A) and their maintainers
selected from the first experiment were evaluated for flowering behaviour. IR58025A was used as
check line. The field experiment was conducted using randomized complete block design with three
replicates. The days to flower, panicle exertion, stigma exertion, duration of glume opening during
anthesis, angle of glume opening and seed set were observed based on SES (IRRI, 2002).
Statistical analysis was conducted using SAS 9.0.


Development of cytoplasmic male sterile lines through succesive backcross
The successful use of hybrid vigor in rice depends on the availability of local cytoplasmic
male sterile (CMS) and restorer lines. Cytoplasmic male sterile line is a rice genotype having
abnormal anther. CMS anther has no pollen or has pollen, but easy to rupture, then there is no seed
set yielded by self fertilization (Yuan et al., 2003). Male sterile character facilitates natural crossing
thus ease the hybrid seed production.
Table 2 shows pollen sterility character of ten CMS from first backcross generation (F
1
BC
1
)
to fifth generation (F
1
BC
5
). From the research, we identified six CMS candidates of Wild Abortive,
three candidates of Kalinga and one candidate of Gambica types. Backcrosses formed segregating
population and gave chance for breeder to select based on spesific target, in this case pollen
sterility. The three cytoplasm types gave different pattern of pollen sterility in the five generations of
backcrosses. In the WA type, there were unique pattern shown by BI497A and BI703A lines, in
which both lines were completely sterile (100%) in the first and second generation of backcrosses,
but reversed to be partial fertile on third and fourth generation. This phenomenon indicated that both
lines showed unstable pollen sterility. Backcross should be done in several generations to
determine pollen stability of both lines. The other lines, i.e. BI485A, BI543A, BI571A and BI599A
showed positive increase in sterility percentage from first to fifth generation of backcrosses. The
CMS with Gambiaca and Kalinga cytoplasm sources also increased pollen sterility as backcross
progressing.

Table 2. Pollen sterility character of new cytoplasmic male sterile lines on F
1
BC
1
- F
1
BC
5
generation

Note: WA= wild abortive; value after was standard deviation

th
All completely sterile CMS with WA cytoplasm source were achieved in the fifth generation
(F
1
BC
5
). In the fourth backcross generation, four lines showed 100% pollen sterility (completety
sterile), while other lines ranged from 99.8 to 99.9%. Different patterns is shown by CMS of Kalinga
and Gambiaca types. The pollen stability of both CMS types were achieved earlier. All of CMS with
Kalinga and Gambiaca cytoplasm had more stable pollen sterility than that of Wild Abortive. A
commercially usable CMS line needs to have complete and stable male sterility, independent from
environmental changes specially temperature (Yuan & Fu, 1995), adaptive to tropical rice growing
conditions and possess good outcrossing potential to affect an economically viable hybrid seed
production (Virmani & Kumar, 2004).

Resistance evaluation of the new cytoplamic male sterile lines to bacterial leaf blight
Male sterile lines should have good adaptation to their rice growing conditions and
resistant to rice pest and disease. The three type of CMS were converted from dihaploid maintainer
(DH
2
) lines. The maintainers were obtained from anther culture of F
1
derived from crossing between
elite maintainer lines and donor lines having high resistance to bacterial leaf blight. Both of
maintainer lines and donor lines were elite breeding lines originated from Indonesia. Therefore, in
the fifth backcross, the new CMS already had cytoplasm from introduced lines, but having
98.4375% nucleus genes from their male parents (recurrent parent). The new CMS are expected
be more adapted to Indonesian environment.
Bacterial leaf blight (BLB) caused by Xanthomonas oryzae pv. oryzae is one of the most
important disease of rice which cause substantial yield losses (Lee et al., 2000). We tested 10 new
CMS lines for reaction to three Indonesian pathotypes. The new CMS shows variation in resistance
to bacterial leaf blight (Table 3). The new CMS of wild abortive cytoplasm and Kalinga cytoplasm
showed to be resistant to moderate resistant to pathotype III, while Gambiaca cytoplasm was
resistant to pathotype III. In Indonesia, the pathotype IV and VIII of bacterial leaf blight were more
virulence than pathotype III. The results showed variation in the reaction of all CMS from three
cytoplasm sources to different pathotypes. One CMS of Kalinga type (BI665A) was resistant to both
of pathotypes. The BI485A, BI497A, BI599A and BI855A showed moderate resistance to bacterial
leaf blight pathotype IV. Reaction of CMS to patotype VIII also varied. BI543A and 571A were
resistant to the pathotype VIII, while BI703A and BI669A were moderate resistant to the pathotype
VIII.

Table 3. Reaction of cytoplasmic male sterile lines to three Indonesian pathotype of bacterial leaf blight

Cytoplasmic Male Sterile
Lines
Resistance to Bacterial Leaf Blight (BLB)
Pathotype III Pathotype IV Pathotype VIII
CMS WA type:

BI485A 3 3 5
BI497A 3 3 5
BI543A 3 7 1
BI571A 3 5 1
BI599A 3 3 5
BI703A 1 5 3
CMS Kalinga type:

BI639A 3 7 5
BI665A 3 1 1
BI669A 1 5 3
CMS Gambiaca type:

BI855A 1 3 5
Note: 1 Resistant, 3 Moderate Resistant, 5 Moderate Susceptible, 7 Susceptible, 9 Very Susceptible

th
Sudir & Suprihanto (2006) reported that virulence of the bacterial Xanthomonas oryzae pv.
oryzae (Xoo) was significant in affecting disease severity of BLB. The elite line donor having xa5
gene which has responsibility to disease resistance. The xa5 gene is recessive and constitutively
expressed at the same level as the dominant susceptible allele, Xa5, and neither allele is induced or
suppresed in response to Xoo (Bart et al., 2006). Availability of CMS lines stable in sterility, good in
agronomic characters, and resistant to disease will increase the adaptability of the hybrid developed
from those CMS lines.

Evaluation of flowering behaviour that support the outcrossing ability between new CMS and
their maintainer
Table 4 shows the observation of several flower behavior of five CMS lines. IR58025A was
used as check line because most rice hybrids in Indonesia were derived from this line. New CMS
lines were earlier to flower than IR58025A, except BI665A. The maintainers flowered 14 days
before their respective CMS pairs. The different days to flower between CMS and their respective
maintainers were in the threshold and important for flowering syncronization when produced CMS
seed (Virmani et al. 1997).

Table 4. Flowering behavior of five new CMS and their maintainers

Note: A: cytoplasmic male sterile lines, B: maintainers; PE: panicle exsertion, SE: stigma exsertion, GOD: duration of glume
opening during anthesis, GOA: angle of glume opening during anthesis; seed set formed in CMS (A) was yielded by
natural outcrossing, pollen came from their respective maintainers; seed set of each maintainer (B) was obtained by
selfing

All new CMS showed good panicle exsertion (more than75%), but BI485A (WA) and
BI665 (Kalinga) were more enclosed than IR58025A. Duration of glume opening during anthesis of
BI485A and BI599A (WA type) was significantly longer than IR58025A. The other new CMS lines
also showed longer duration of glume opening than that of IR58025A but not statistically significant.
BI599A, BI855A and BI639A showed wider angle of glume opening than that of IR58025A i.e. 39.8;
36.0 and 40.6 degrees, respectively. The better duration and angle of glume opening would
increase the opportunity of new CMS stigmas to receive pollen from maintainers.
Stigma exsertion of the three types of CMS was higher than IR58025A. It ranged from
67.7 to 74.7% compared to that of IR58025A (43.3%). The better flowering behavior caused higher
seed set of the new CMS than IR58025A. The new lines set seed at about 4.825.9%, while
IR58025A achieved 2.9% of seed set. Corellation analysis showed positive high and significant
value between seed set of new CMS lines with stigma width (r=0.44*), stigma exertion (r=0.54*) and
angle of glume opening during anthesis (r=0.42*). The seed set was also affected by some flower
characters of maintainer lines such as filament length and angle of glume opening during anthesis
(data not shown). The results indicated that the new CMS lines with different cytoplasm source
could be used in hybrid rice breeding.

th
Conclusions

Combination of anther culture and backcrosses obtained 6 CMS lines of WA type, 3 CMS
lines of Kalinga type, and 1 CMS line of Gambiaca type. The lines had stable sterility and
resistance to 1-3 Xanthomonas oryzae pathotypes. The new CMS showed better flowering behavior
which increase the seed set.

References

Bart, R., P. Ronald, and S. Hake. 2006. Fertility versus disease resistance, a hard choice. Gene and
Development (20): 1215-1217.
Dewi, I.S., A. Apriana, A. Sisharmini, and I.H. Somantri. 2007. Resistance evaluation of doubled haploid of
parental lines candidate to bacterial leaf blight and brown planthopper. Bull. Agron 35(1):15-21.
Eckardt, N.A. 2006. Cytoplasmic male sterility and fertility restoration. The Plant Cell 18:515-517.
Gavino, R.B., Y. Pi, and C.C. Abon Jr. 2008. Application of gibberellic acid (GA3) in dosage for three hybrid rice
seed production in the Philippines. Journal of Agricultural Technology 4(1): 183-192.
[IRRI] International Rice Research Institute. 2002. Standarization Evaluation System for Rice. 66p
Rumanti I.A., Dewi I.S., Purwoko B.S. and Aswidinnoor H. 2008. Evaluation of anther culture-derived doubled
haploid maintainer lines for developing rice male sterile lines. Jurnal Agronomy Indonesia 37 (1): 1 7
(In Indonesian).
Takai, T., S. Matsura, T. Nishio, A. Ohsumi, T. Shiraiwa, and T. Horie. 2006. Rice yield potential is closely
related to crop growth rate during late reproductive periode. Field Crops Research 96: 328-335.
Li, J., S. Cai, J. Feng, Li, and G. Cheng. 2007. Comparisons on genetic diversity among the isonuclear-
allopasmic male sterile lines and their maintainer lines in rice. Rice Science 14(2): 94-100.
Peng, S., G.S. Khush, P. Virk, Q. Tang, and Y. Zou. 2008. Progress in ideotype breeding in increase rice yield
potential. Field Crop Research 108: 32-38.
Sudir and Suprihanto. 2006. Change in virulence of strain Xanthomonas oryzae pv. oryzae, a causal pathogen
of bacterial leaf blight in rice. Jurnal Penelitian Pertanian Tanaman Pangan 25 (2): 100-107. (In
Indonesian).
Suwarno, N.W. Nuswantoro, Y.P. Munarso, and M. Diredja. 2003. Hybrid rice research in Indonesia..In: S.S.
Virmani, C.X. Mao, and B. Hardy, eds, Hybrid Rice for Food Security, Poverty Alleviation, and
Environmental Protection. Proceedings of the 4
th
International Symposium on Hybrid Rice, Hanoi-
Vietnam, 14-17 May 2002. IRRI, Philippines. pp. 287-296.
Virmani, S.S., and I. Kumar. 2004. Development and use of hybrid rice technology to increase rice productivity
in the tropics. Internationasl Rice Research Notes 29 (1):10-19.
Virmani, S.S., B.C. Viraktamath, C.L. Casal, R.S. Toledo, M.T. Lopez, and J.O. Manalo. 1998. Hybrid Rice
Breeding Manual. IRRI, Philippines.
You, A., X. Lu, H. Jin, X. Ren, K. Liu, G. Yang, H. Yang, L. Zhu, and G. He. 2006. Identification of quantitative
trait loci across recombinant inbred lines and testcross populations for traits of agronomic importance in
rice. Genetics 172:1287-1300.
Yuan, L.P., X. Wu, L. Fuming, G. Ma, and Q. Xu. 2003. Hybrid Rice Technology. China Agriculture Press.

th
Genetic Analysis of Superior Double Haploid Rice Lines Developed from
Anther Culture

Muhammad Syafii
a,*
, Bambang S. Purwoko
b
, Iswari S. Dewi
c

a
Postgraduate of Plant Breeding and Biotechnology, Bogor Agricultural University, Bogor, Indonesia
b
Department of Agronomy and Horticulture, Bogor Agricultural University, Bogor, Indonesia
c
Indonesian Center for Agricultural Biotechnology and Genetic Resources Research and Development,
Cimanggu, Bogor, Indonesia
* Corresponding author: Postgraduate of Plant Breeding and Biotechnology,
Bogor Agricultural University, Bogor, 16680-Indonesia.
Tel.: +62 251 862 9353; fax: +62 251 862 9353.
[email protected]

Abstract

Rice is the most important food commodity in Indonesia. The need for rice continues to increase with the
population increase. Plant breedings objective to obtain high-yielding varieties is an attempt to increase
production plateu. Biotechnology is one of the breeding aproaches using tissue culture and genetic engineering
techniques. The availability and diversity of plant genetic resources are important factors to develop high
yielding varieties with desirable traits. This study was aimed to investigate the agronomic characters of double
haploid lines developed from anther culture, evaluate genetic diversity, phenotypic variations and broad sense
heritability of double haploid lines developed from anther culture, and to obtain rice genotypes potential as
superior lines. Analysis of 18 genotypes showed there was diversity of agronomic characters among the rice
double haploid genotypes. Characters of dry weight-based grain (yield) per hectare and the number of empty
grain per panicle had high level of genetic variability, while other characters had rather low to low level of genetic
variability. Yield per hectare in KP44223 line was the highest (4537.8 kg / ha or 4.5 tons / ha) among the lines,
even higher than that of conrol varieties, Ciherang and Celebes. The characters of plant height, flowering age,
harvesting time, panicle length, number of empty grain/ panicle, 1000 grain weight and yield per hectarehad high
broad sense heritability, suggested that those characters can be used as selection characters to improve crop
performance

Keywords: anther culture, double haploid, rice

Introduction

Rice is the most important food commodity in Indonesia. In addition, rice is also a major
source of carbohydrate material for Indonesian people. The need for rice continues to increase with
population increase. (Prasetyo 2008), Plant breeding to obtain high-yielding varieties is one attempt
to overcome rice production plateu. Utilizing biotechnology through tissue culture technique and
genetic engineering could be one of the appraches in plant breeding (Somantri et al. 2003). The
availability and diversity of rice genetic resources is an important factor in developing high yielding
varieties with desirable traits. Development of new high yielding varieties of rice in Indonesia has
long been conducted since the early 1970s. After the 1980's breeding toward new high yielding
varieties (VUB) started to be intensified to obtain varieties that are responsive to fertilizer and high
quality of rice, such as IR64, Membramo, Cisadane and Ciherang (Samaullah 2007). Conventional
breeding to develop new rice varieties require a long time (7-10 years), especially the time for
selection process to obtain pure lines. Utilization of modern technologies (biotechnology) such as
anther culture is expected to shorten the selection process thus saving time, effort, and cost. Dewi
and Purwoko (2001), states that the researchers have applied the anther culture technique to obtain
rice lines that are resistant to pests and diseases, quality of rice as well as tolerant of environmental
th
stress. Kim (1986), also reported that anther culture-based breeding approach have also been
applied in Korea, Vietnam, China and India.


The study was conducted in January-May 2011 at IPB laboratory, Dramaga, Bogor. The
materials used were 18 rice double haploid lines developed from anther culture (KP1-3-1-2, KP3-7-
2-1, KP3-18-1-1, KP3-18 -1-2, KP3-18-1-3, KP3-19-1-1, KP3-19-1-2, KP3-19-1-3, KP3-19-1-4, KP4-
19-1 -3, KP4-19-2-3, KP4-42-2-1, KP4-42-2-2, KP4-42-2-3, KP4-43-1-2-43-KP4 1-4 , KP4-43-2-3,
KP4-43-2-4), and 2 control varieties (Ciherang and Celebes). The experiment was conducted at the
Experimental station Babakan IPB, Darmaga, Bogor, using Randomized Block Design with four
replicates. The treatments used were 18 double haploid rice genotypes and two control rice
varieties. The 21 day old seedlings of each genotype were planted in field plots (0.8 x 5 m) with
plant spacing of 20x20 cm having 2 seedlings/hole. Plants were fertilized with 200 kg/ha of Urea,
100 kg/ha of SP36 and 100 kg/ha of KCl applied three times at 10, 25 and 45 days after planting
(DAP). Plants were maintained based on the paddy rice cultivation. The observations were
performed on parameters of plant height (cm), total number of tillers (stems), number of productive
tillers (stems), flowering date (days), harvesting date (days), panicle length (cm), number of filled
grain per panicle (grains), number of empty grain per panicle (grains), total grain number per
panicle (grains), weight of 1000 grains (g), and grain yield (kg/ha).
The data were analyzed using analysis of variance, Duncan multiple range test and
analysis variance components (Singh and Chaudhary 1979). Variance component and heritability
were determined based on Singh and Chaudhary (1979) as follow:

V
g =
; V
P
= V
g
+ Ve ; h
2
b s =
; KVG = (
). 1 0 0 % ; K V P = (
). 1 0 0 %

Which was:
Vg: various genotypes; Vp: various phenotypes; r: replication; X: average common genotype; KVG:
coefficient of genetic diversity; KVP: coefficient of phenotypic diversity; KTg: sum square of
genotype; KTE: sum square error. Broad sense heritability values according to Stanfield (1983) is
high (12:50 <h2 <1.00), moderate (12:20 <h2 <0.50) and low (h2 <0.20).


The results showed that the genotype effect was significant to all characters observed.
This suggested that there was variability among genotypes for all the observed characteristics.

Plant Height
KP44323 and KP44324 lines were genotypes having highest average plant height (112.6
and 112.3 cm, respectively), while KP31812 and KP31813 lines had shortest average of the plant
height (83.6 and 84.95 cm, respectively). Ciherang was classified as medium plant height (103 cm),
while Celebes was classified as relatively short plant height (82.8 cm). From anther culture, the
characters inheriteged from parent was the plant height, both on descent Ciherang and Celebes.
This indiated that the plant height was dominant.

th
Total Productive Tillers and Tillers
Although not signicantly different among genotype, number of tillers and productive tillers
per plant were varied among genotypes ranging from 14.1 to 19.55 and 11.55 to 15.25,
respectively. KP31913 and KP44223 were the genotypes producing the highest and the lowest
tillers. While KP1312 and KP44314 were the genotypes having the highest and the lowest
productive tillers. The genotypes tested showed moderate number of tillers.

Flowering and Harvested
Flowering KP31812 of genotype lines and varieties Cilebes (control) i.e 63.25 consecutive
days and 57 days compared to genotype lines KP41913, KP44312, KP44221, and KP44324 the
consecutive 76 days and 75.75 days. This indicated that the lines have descended from varieties
Ciherang age slower than lines flowering varieties descent Celebes. To determine the general
harvesting age, the age of the rice crop can be classified into three groups calculated from the day
after the scatterplot (HSS), namely age genjah (90-104 HSS), age was 105-120 HSS and age in at
more than 120 HSS) (BB-padi 2009a). The average age of crop genotypes tested genjah belonging
to moderate, with harvest age genjah of lines KP31811 and KP31813 was 91.75 day and most
varieties genjah in Celebes (control) to 89.75 days old. While the maximum harvest age on
genotype KP41913 and KP41923 a consecutive were 106 days and 105.75 days, respectively.

Panicle length
Panicle length characters in genotypes tested was quite short to medium. Longest panicle
was found at KP44323 which was 24.96 cm. This was slightly shorter than that of varieties Ciherang
at 25.82 cm, while the shortest panicle of KP44222 was 22.82 and 21.82 cm resulted from Celebes
varieties (Table 3). DMRT test showed that all genotypes were not significantly different between
the lines tested, except in the control varieties and Celebes Ciherang.

Number of Grain per Panicle
Line KP3721 had highest total amount of grain per panicle of 178.85 points, while the
lowest was found in line KP31914 and KP31813 at 121.55 points and 121.88 points, respectively.
Thus these genotypes were ssified as moderate (Table 4). All the genotypes tested were not
significantly different with the second control test DMRT at 5%, except in line KP3721 and
KP31914. Lines KP44312 and KP44324 had high in grain content / panicle at 100.35 points,
respectively and 100.1 points higher than the control plants respectively 90.45 and 90.1 for the
Celebes and Ciherang, while the lowest was found in line KP41923 had 56.45 points lower than the
control varieties. KP41923 line had the most empty grain number/panicle at 106.3 points, while the
lowest in line was KP31914 had 33.75 points. Although the line had a number of grain hollow
KP31914/panicle, this line produced the lowest total amount of grain. That affected the yield per
hectare. Calculation of the percentage (%) content of grain/panicle to total grain/panicle produced in
line KP31914 was the highest at 72.23%, this value was higher than that of the varieties of Celebes
(control) atf 70.06%. The lowest percentage was found at lines KP41923 and KP44314 which were
34.6 and 46.04%, respectively.

1000 Grain Weight
Weight of 1000 grains of rice indicated the size of grains of rice and beans level. The
results showed that the highest weight of 1000 grains of rice was found at KP1312 line at 39 925 g.
This value was higher than both the control varieties and Celebes Ciherang consecutive which were
36 025 and 30,575 g, respectively. The weight of 1000 grains of line KP3721 was the lowest at 26
325 g. This value was lower than the control Celebes varieties which was 30 575 g. KP3721 line
had the lowest weight of 1000 grains allegedly due to low resistance to various diseases in the field,
either by bacteria or viruses. Value of 1000 grain weight assessed with DMRT test at 5% level is
shown in Table 3.
th
Grain Yield (kg /ha)
Grain yield per plot can be used to measure the amount of the plant production. Dry grain
yield per plot was then converted to a hectare (kg/ha). The highest production was found at line
KP44223 (no.entry 14) and KP44221 (no. entry 12) in a row having 4.5 and 4.3 t/ha, respectively,
this significantly different with both the control varieties and Celebes Ciherang at 3:50 and 3:43 t/ha,
respectively. The lowest dry grain was found at line KP41923 (no.entry 11) and KP31811 (no.entry
3) consecutive at 1:03 and 1.82 tonnes/ha, respectively. This differed markedly lower than the
control based on test DMRT 5%. DMRT test at 5% for the grain yield/ha showed that all lines tested
had distinct intangible, except in line KP44223 (highest) and line KP41923 (lowest) (Table 3).

Variety Component
Various components and heritability estimation is performed to determine the proportion of
diversity caused by genetic factors and environmental factors. Heritability determines the success of
selection for the appropriate environment, because it indicates the heritability of a trait is influenced
by genetic or environmental factors. High heritability indicates the relative importance of genetic
influences that can be used from the elders to their offspring as well as useful to determine the most
appropriate selection method for improving a plant characters (Falconer and Mackay 1996). The
value of plant genetic parameter estimation is shown in Table 3. Coefficient value of genetic
diversity (KVG) ranged between 3.25 and 27.31 and phenotypic diversity coefficient (KVP) ranged
between 4.51 and 36.83. Value KVG KVG 0.00-27.31% was the absolute value, that value was
determined from the relative value of KVG. Absolute value of 27.31% KVG KVG was a relative
value of 100%. According Moedjiono and Mejaya (1994), KVG relative value of the following criteria:
low (0 <x <25%), somewhat lower (25%<x<50%), high (50%<x<75%) and high (75%x<100%).
Based on the above criteria, it can be determined KVG absolute criteria in this trial, namely low
(0.00 <x <6.83%), somewhat lower (6.83% <x <13.66%), high (13.66% <x <20:48%), and high
(20:48% <x <27.31%). Murdaningsih et al. (1990) stated that the value was low and rather low KVG
classified as narrow genetinya character variability, while quite high and high KVG classified as
character mempynyai wide genetic variability.

Table 3. The value range of components and heritability estimates the value of agronomic characters and yield
in rice

Agronomic character mean Vg Vp KVG (%) KVP (%) h
2
bs (%)
Plant hight 93.79 87.61 103.04 9.98 10.82 85.03
Productive tillers 13.55 0.24 5.44 3.62 17.22 4.42
Total tiller 16.43 0.37 7.54 3.70 16.71 4.89
Flowering 69.59 30.54 31.56 7.94 8.07 96.79
Harvested 98.00 18.59 19.53 4.40 4.51 95.17
Panicle lenght 23.79 0.60 1.19 3.25 4.59 50.13
Number of grain/panicle 85.53 116.29 255.69 12.61 18.70 45.48
number of empty grain/ panicle 55.37 228.61 415.72 27.31 36.83 54.99
Total grain/panicle 140.90 165.78 372.94 9.14 13.71 44.45
1000 grain weight 34.43 9.46 14.01 8.93 10.87 67.53
Yield (ton/ha) 2.94 5.64 11.24 25.58 36.12 50.17
Remarks: Vg=varian genotype, Vp=varian phenotype, KVG=coefisien varian genotype, KVP=coefisien varian phenotype, h
2
bs=
boad sense heritability

th
Based on the criteria of absolute KVG, there were two characters having relatively high
KVG ie grain yield / ha and the number of empty grain per panicle, five characters have a rather low
KVG, namely plant height, flowering age, number of grain content per panicle, total grain number
per panicle and 1000 grain weight, and the four characters have low KVG ie the number of
productive tillers, total number of tillers, harvesting age, and length of panicle. Thus there are two
characters having a broad genetic variability, and there are nine characters that have a narrow
variability. Nugraha Lestari (2007) mentioned the opportunities for improvement of grain yield can
be done with the selection of the character of the number of grain per panicle and grain yield dry.
Broad sense heritability value of the characters observed was between 04:42 and 96.79% (Table
3). According to Stanfield (1983), broad sense heritability values can be grouped into three high
heritability (12:50 <h2 <1.00), the heritability of moderate (0.2 <h 2 <0.50) and low heritability (h2
<0.20). Based on the above criteria that broad sense heritability values for characters: plant height,
flowering age, age of harvest, panicle length, number of empty grain / panicle, 1000 grain weight
and dry grain yield per hectare was high, whereas the character of grain number per panicle and
the number of content total grains per panicle classified as being; then to the character of
productive tillers and total number of tillers per hill had a low broad sense heritability values.
Therefore, the improvment of grain yield can be done through the selection of plant height, flowering
age, age of harvest, panicle length, number of empty grain / panicle, 1000 grain weight and grain
yield per hectare dry.

Conclusions

Analysis of agronomic characters of 18 genotypes indicated that there was diversity in
agronomic characters and character among the double haploid genotypes of rice anther culture
results. Dry grain yield per hectare and the number of empty grain per panicle had a high level of
genetic variability, agronomic characters and yield while others had a rather low level of genetic
variability to low. Dry grain yield per hectare obtained from line KP44223 was the highest of 4.5
ton/ha than varieties Ciherang and Celebes. High broad sense heritability value generated on the
characters were plant height, flowering age, age of harvest, panicle length, number of empty
grain/panicle, 1000 grain weight and grain yield per hectare dry Therefore, the characters can be
used as benchmarks for improving the character of the next generation of this crop.

References

Alluri K.1986. Screening rice varieties in acid upland soil. Progress in Upland Rice Research. IRRI. Los banos.
Philippines. pp 263-270.
Bhojwani SS, Razdan MK, 1996. Plant Tissue Culture. Theory and Practice, a revised edition. Elsevier Science.
Amsterdam. The Netherlands. 767p
Chang TT, Bardenas EA. 1965. The morphology and variety characteristics of the rice plant. Technical Bulletin
4. IRRI. Laguna. Philippines. 40p.
Chung GS. 1992. Anther culture for rice improvement in Korea. In: K. Zheng, T. Murashige (eds). Anther Culture
for Rice Breeder. Seminar and Training for Rice Anther Culture at Hangzhou. China. P8-37.
Dewi IS, Purwoko BS. 2001. Kultur antera untuk mendukung pemuliaan padi. Bul. Agron. 29(2):59-63
Donald CM. 1968. The breeding of crops ideotypes. Euphytica 17:385-403
Falconer DS, Mackay TFC. 1996. Introduction to Quantitative Genetics. Fourth edition. Longman. London
Fehr WR. 1987. Principles of Cultivar Development. Vol 1. McGraw-Hill. Inc. New York
Hu H. 1998. In-vitro induced haploids in higher plant. Di dalam : Genetic Manipulation in Crops. Proceeding of
the International symposium on Genetic Manipulation in crops: the 3
rd
International Symposium on
haploid. Beijing. Oktober 1984. IRRI. And Sinica Academy. p8-12
International Rice Research. 2004. Rice Knowledge Bank. CD ROM Version 3.1 (15 April 2004).
Kush GS. 1995. Breaking the yield frontier of rice. Geo Journal 35: 329-332.
th
Kim K. 1986. Ststus of Korean biotechnology and its role in improving crop production. In: Workshop on
Biotechnology for crop Improvement, potentials, and limitations. 13-17 oktober 1986. IRRI. Philipines
35p.
Moedjiono dan Mejaya MJ. 1994. Variabilitas genetik beberapa karakter plasma nutfah jagung koleksi Balittas
Malang. Zuriat 5 (2):27-32
Murdaningsih HK, Baihaki A, Satari G, Danakusuma T, Permadi AH. 1990. Variasi genetik sifat-sifat tanaman
bawang di Indonesia. Zuriat 1(1): 32-36
Prasetyo YT. 2008. Bertanam Padi Gogo Tanpa Olah Tanah. Bibliografi. hal 69.
Samaullah Y M. 2007. Pengembangan varietas unggul dan komersialisasi benih sumber padi. Apresiasi Hasil
Penelitian Padi. Balitpa.Sukamandi
Singh RK, Chaudhary BD. 1979. Biometrical Method in Quantitative Genetic Analysis. Kalyani Publ. New Delhi.
304p.
Soemantri IH, Ambarwati AD, Apriana A.2003. Perbaikan Varietas padi melalui kultur antera. Prosiding Hasil
Penelitian Rintisan dan Bioteknologi Tanaman. hal. 2008-214
Stanfield WD. 1983. Theory and Problems of Genetics, 2
rd
edition. Schains Outline Series. Mc. Graw Hill Book
Co. New Delhi.
Yoshida. 1981. Science of The Rice Plant. Food and Agricul;ture Policy Center. Tokyo. Japan. p21-25

th
QTLs on Chromosome 12 Responsible for Expressing Root Plasticity under
Transient Soil Moisture Fluctuation Stress in Rice

Jonathan M. Niones, Yoshiaki Inukai, Akira Yamauchi*

Graduate School of Bioagricultural Sciences, Nagoya University
*Corresponding author: Nagoya University, Chikusa, Nagoya 464-8601 Japan
Tel : +81-52-789-4021; Fax : +81-52-789-4022
[email protected]

Abstract

Soil moisture fluctuations (i.e. transient waterlogged to drought) frequently occur in rainfed rice fields due to
erratic rainfall pattern, and irrigated fields due to wetting and drying system practices and inefficient irrigation
system. Such conditions are stressful for growth and development of rice. With the utilization of chromosome
segment substitution line (CSSL), we previously demonstrated the significant roles of root plasticity as
expressed by higher lateral root production in response to soil moisture fluctuation stress. Moreover, our
molecular mapping analysis showed the presence of QTL that is associated with root plasticity, at short arm of
chromosome 12 region. This QTL was found to control the productions of L-type lateral roots with the increase
effect from Kasalath allele. In this study, we attempted to quantify the significant functions of QTL (qLLRn-12) on
chromosome 12 in relation to the shoot dry matter productions and root system development. CSSL genotypes
with QTL or substituted segment of Kasalath allele on chromosome 12 were evaluated and subjected to 38 days
of transient soil moisture fluctuation stress. Results revealed that CSSL genotype with qLLRn-12 showed greater
root system development as expressed its greater total root length than those without qLLRn-12 in response to
moisture fluctuation stress. Longer total root length was attributed to higher production of L-type lateral roots,
which can effectively maintain water and nutrient uptake in the soil. Such plastic root responses resulted in
increased stomatal conductance and photosynthesis, eventually increased shoot dry matter production by 37%
compared to its Nipponbare parent. Comparison of the location of the QTL across rice cultivars showed that
there is no QTL reported in this region related to lateral root production. This may possibly be a putative QTL
and potentially be used in the marker-aided breeding program to improve adaptation under fluctuating soil
moisture environment.

Keywords: chromosome segment substitution lines (CSSL), lateral root, rice, root plasticity, soil moisture
fluctuation

Introduction

With the scarcity of water for irrigation and continuing increase of world population, future
increase in rice production will more heavily rely on rainfed rice ecosystem. Rainfed lowland
conditions are characterized by frequent fluctuation in soil moisture at varying degrees throughout
the cropping season, which have stressful effects on the growth and development of rice (Niones et
al., 2009). Plant roots play an important role in water and nutrient acquisition. Both constitutive and
adaptive root growth have been implicated in the improvement of plant performance under rainfed
conditions (Kamoshita et al., 2002). A plant has an ability to change its phenotype, in response to
soils heterogeneous environment (Yamauchi et al., 1996), which is termed as plasticity, and root
plasticity is a key trait for plant adaptation to stressful conditions. Moreover, we reported that traits
associated with developmental root plasticity triggered by mild drought stress played significant
roles in water uptake and dry matter production in rice (Kano et al., 2011).
With the use of chromosome segment substitution lines (CSSL), we previously identified
one line CSSL47 that consistently showed more plastic root growth than Nipponbare in terms of
branching of lateral roots and aerenchyma formation at early vegetative stage (Suralta et al., 2008,
th
2010) and until maturity (Niones et al., 2009) under transient soil moisture fluctuations. This line
contains 10 substituted segments from Kasalath allele with Nipponbare genetic background. Niones
et al. (2010) identified the location of the QTL at short arm of chromosome 12 region, which are
responsible for controlling root developmental plasticity specifically the L-type lateral root
production. The expression of such root plasticity QTL and its effect on dry matter production and
root system development when rice plants are grown under transient soil moisture fluctuation
conditions have not yet been further verified.
In this study, we examined the significant function of the QTL or substituted segment from
Kasalath allele on chromosome 12 in relation to the shoot dry matter production at vegetative stage.
Furthermore, we tested the variation in root plasticity expression of parents and CSSL genotype
with QTL or substituted segment of Kasalath allele on chromosome 12 under 38 days of transient
soil moisture fluctuation stress.


Plant materials
Four genotypes (Nipponbare, CSSL47, CSSL27, CSSL52) were used in this study.
Nipponbare, an irrigated lowland japonica variety and recurrent parent of the 54 chromosome
substituted segment line (CSSL) (Nipponbare/ Kasalath cross) population genotypes. CSSL47
genotype has ten substitute segments across genome from Kasalath allele with a unique
characteristics of having greater plastic responses in root development under soil moisture
fluctuations than the other CSSLs (Suralta et al., 2010; Niones et al. (2009). The CSSL27 and
CSSL52 genotypes were selected from the 54 CSSL population. CSSL27 genotype contained no
substituted segment of Kasalath in short arm of chromosome 12 region, and thus is hereon referred
as - SL, while CSSL52 (referred as +SL) has substituted segment of Kasalath in short arm of
chromosome 12 region only. The seeds of CSSL population was provided by the Rice Genome
Research Center of the National Institute of Agrobiological Sciences, Tsukuba, Ibaraki, Japan.

Treatment conditions
Seedlings were grown in soil-filled plastic root box and exposed to three different soil water
conditions; the well-watered (WW), transient waterlogged to drought (W-D) and transient drought to
waterlogged (D-W) conditions. Plants were exposed to waterlogged conditions for 17 days and
thereafter the water was allowed to drain to the target soil moisture content (SMC) of 20%, which
was then maintained for 21 days by watering every two days. Plant samplings were done at 38
DAS.

Root phenotyping
Lateral roots (LRn) were manually counted. Each nodal root was cut into 5-cm segments
keeping the lateral roots intact. In this way, the number of each type of lateral root; L and S type of
lateral roots in rice (Yamauchi et al., 1996) can be determined and expressed as linear frequency
(number of lateral roots per unit length root axis; Ito et al., 2006). One of their major noticeable
differences is that L type is branching while S type is non-branching. For total root length (TRL)
measurements, root samples from the FAA were rinsed with running water and spread on
transparent sheet without overlapping. The digitized images were taken using Epson scanner
(ES2200) at 300 dpi resolution. TRL was analyzed using a NIH image software (ver.1.60), a public
domain released by the National Institute of Health, USA.

Statistical analysis
The experiments were laid out in split-plot randomized complete block design with three
replicates. The significance differences of four genotypes were compared at LSD > 0.05
significance level using the Cropstat software.

th

Plastic root development was mainly attributed to enhanced lateral root production
particularly the L-type lateral (Baoc et al., 2002; Suralta et al., 2010), which is a key trait for the
plant adaptation under transient soil moisture production. Lateral roots generally comprised the
greater proportion of the whole root system (Yamauchi et al., 1987), and thus promoted lateral root
development in response to moisture stress directly reflects the performance of the entire root
system. Enhanced lateral root development results in increased root surface area, and soil water
extraction and water use. Therefore, the maintenance of stomatal conductance and photosynthesis
could be a consequence of greater supply of water to leaves due to the enhanced lateral root
development as a result of their plastic responses.
QTL reported by Niones et al. (2010) was located at the short arm of chromosome 12
region, which is hereon referred as qLLRn-12. This was associated with root developmental
plasticity with the increase effect from Kasalath allele. The function of this QTL was to regulate the
production of L-type lateral roots, which is associated with plastic root system development. It is
assumed that the possible location of the qLLRn-12 may be near TG156 marker locus with the
approximate distance of 17.6 cM between the adjacent markers RM6296.
In this study, greater lateral root development of + SL genotype over Nipponbare and SL
genotypes was shown in higher linear frequency of lateral root number in response to transient soil
moisture fluctuation stress. This result showed the evidence the importance of QTL or Kasalath
segment that was present in chromosome 12 (Figure 1). Figure 2 shows the significant positive
correlation between total root lengths and the production of lateral root under both transient soil
moisture fluctuation stress treatments, with r-value of 0.624 for D-W and 0.646 for W-D. This result
indicates that under transient fluctuations of soil moisture, higher production of lateral root had a
significant contribution to greater root system development that eventually leads to enhanced water
and nutrient uptake in the soil.

Figure 1. The linear frequency of lateral root number per cm of the four genotypes grown under different soil
moisture conditions: i.e. WW, well-watered; W-D, transient waterlogging to drought; D-W, transient
drought to waterlogging. () ) - SL indicates the CSSL genotypes that do not
contain QTL or introgressed segment from Kasalath, ( ) + SL indicates the CSSL genotypes that do
not contain QTL or introgressed segment from Kasalath and ( CSSL47. Same letter means that
values are not significant at LSD > 5% level of significant level.

th

Figure 2. Relationships of linear frequency of lateral root with total root length under different soil moisture
conditions; A, transient waterlogging to drought; B, transient drought to waterlogging. ( ), - SL
(CSSL28); ( ), CSSL47; ( ), + SL (CSSL52); (
O
), Nipponbare.

To further demonstrate the effect of the existence of QTLs in response to transient soil
moisture fluctuation stress, + SL genotypes were evaluated for plastic root system development in
relation to shoot dry matter and root system development as shown in Figure3. The + SL genotype
showed significantly greater shoot dry matter production with the increase of 30% in W-D and 43%
in D-W than Nipponbare. The increase in shoot dry matter of + SL genotype was associated with a
10% (W-D) and 17% (D-W) increase in total root length compared to Nipponbare. On the other
hand, these parameters were not significantly different between SL genotype and Nipponbare
parent. These facts clearly suggest that the function of QTLs at chromosome 12 was to regulate the
production and branching of lateral roots (i.e., L-type lateral root), which resulted in greater plastic
root system development. This eventually led to the enhanced shoot dry matter production at
vegetative stage under fluctuating soil moisture conditions.

Figure 3. Effect of the presence of QTL at short arm of chromosome 12 on the shoot dry matter production and
total root length under different transient soil moisture fluctuation conditions. Same letter means that
values are not significant at LSD > 5% level of significant level.

We identified in short-arm of chromosome 12 region, the location of QTL that is
responsible for regulating the production of L-type lateral roots with the increase effect from
Kasalath allele. The use of the CSSL genotypes that contain substituted segment of Kasalath in
chromosome 12 only further validated this QTL function. There have been reports on QTLs that are
associated with root length, root number, root dry weight and branching index traits (Price et al.,
2002; Horii et al., 2006; Gowda et al., 2011), however, with the best of our knowledge, there have
been no reports on QTL in this region, which are related to lateral root production under soil
moisture fluctuation stress. Fine mapping is necessary to narrow down the distance of linked
th
markers to the target trait. Then, this could be potentially used in the marker-aided breeding
program for enhanced plant adaptation under such environment.

References

Baoc DM, A Yamauchi, A Kamoshita, LJ Wade, JR Pardales Jr 2000. Genotypic variations in response of
lateral root development to fluctuating soil moisture in rice. Plant Prod Sci 3:335-343.
Gowda VRP, A Henry, A Yamauchi, HE Shashidhar, R Serraj 2011. Root biology and genetic improvement for
drought avoidance in rice. Field Crops Res 122:1-13.
Horii H, K Nemoto, N Miyamoto, J Harada 2006. Quantitative trait loci for adventitious and lateral roots in rice.
Plant Breed 125:198-200.
Ito K, K Tanakamaru, S Morita, J Abe, S Inanaga 2006. Lateral root development, including responses to soil
drying, of maize (Zea mays) and wheat (Triticum aestivum) seminal roots. Physiol Plant 127: 260-267.
Kano M, Y Inukai, H Kitano, A Yamauchi 2011. Root plasticity as the key root trait for adaptation to various
intensities of drought stress in rice. Plant Soil 342:117-128 (DOI 10.1007/s11104-010-0675-9).
Niones JM, RR Suralta, Y Inukai, A Yamauchi 2009. Evaluation of functional roles of plastic responses of root
system in dry matter production and yield under continuous cycle of transient soil moisture stresses by
using chromosome segment substitution lines in rice under field conditions. Jpn. J. Crop Sci. 78 (Extra 1)
260-261.
Niones JM, Y Inukai, A Yamauchi 2010. Identification of linked QTLs for root plasticity in rice under continuous
transient soil moisture fluctuation stress in field. Jpn. J. Crop Sci. 79 (Extra 2) 268-269.
Price AH, KA Steele, BJ Moore, RGW Jones 2002. Upland rice grown in soil filled chambers and exposed to
contrasting water-deficit regimes II. Mapping quantitative trait loci for root morphology and distribution.
Field Crop Res 76:25-43.
Suralta RR, Y Inukai, A Yamauchi 2008. Utilizing chromosome segment substitution lines (CSSLs) for evaluation
of root responses under transient moisture stresses in rice. Plant Prod Sci 11:457-465.
Suralta RR, Y Inukai, A Yamauchi 2010. Dry matter production in relation to root plastic development. Oxygen
transport, and water uptake of rice under transient soil moisture stresses. Plant Soil 332:87-104.
Yamauchi A, Y Kono, J Tatsumi 1987. Quantitative analysis on root system structure of upland rice and maize.
Jpn J Crop Sci 56:608-617.
Yamauchi A, JR Pardales Jr, Y Kono 1996. Root system structure and its relation to stress tolerance. In O. Ito,
K. Katayama, C. Johansen, J.V.D.K. Kumar Rao, J.J. Adu-Gyamfi and T.J. Rego eds., Roots and Nitrogen
in Cropping Systems of the Semi-Arid Tropics. JIRCAS Publication. Tsukuba, Japan. 211-234.

th
Yield and Related Traits in Two J aponica Rice Lines Carrying Ur1 Gene

Stanis Malangen
a
, Takumi Iwakura
b
, Toru Hata
b
, Takeshi Akaoka
b
, Amol Dahal
b
,
Masayuki Murai
b,
*

a
United Graduate School of Ehime University, Matsuyama, Ehime, 790-8566, Japan
b
Faculty of Agriculture, Kochi University, Monobe, Nankoku, Kochi, 783-8502, Japan
* Corresponding author: Faculty of Agriculture, Kochi University, Monobe, Nankoku, Kochi, 783-8502, Japan
Tel.: +81- 088-864-5120; Fax: +81- 088-864-5200 (common)
[email protected]

Abstract

Ur1 (Undulate rachis-1) is an incompletely dominant gene on chromosome 6 in rice, being characterized by
undulation of primary and secondary rachis branches. Ur1 increases not only the number of secondary branches
per panicle but also spikelet number per single secondary branch, resulting in a large spikelet number per
panicle. This genic effect can increase grain yield by enlarging sink size. We examined the yielding abilities of
the two Ur1-carrying lines under field conditions (mid-April sowing and early-May transplanting in two
experimental years). The two Ur1-carrying lines (MR79 and MR53) were selected from 108 recombinant inbred
lines (F8 generation) originating from 108 F2 plants of the cross of Nishihikari an isogenic line of Taichung 65
carrying both Ur1 and sd1-d. Hinohikari, a leading variety in southern Japan was the check variety in the
present study, being denoted by Hi. Additionally, Nishihikari (Ni), a high yielding variety adaptable to fertile
land, was employed. They were grown under three fertilizer levels (4, 8 and 16 of Ng/ in total) and two fertilizer
levels (12 and 21 of Ng/ in total), together with P and K elements, in 2003 and 2005, respectivelyYield and
other traits were measured. The results at 21 of N g/in 2005 are described as follows. In yield (brown rice,
g/), the lines-varieties were ranked in the order MR79 (728) > MR53 (723) > Ni (695) > Hi (558). MR79 and
MR53 had 170 g/ (30%) and 165 g/ (30%) higher yields, respectively, than Hi. Regarding spikelet number
per panicle, they were in the order MR79 (132.7) > MR53 (116.0) > Hi (94.5) > Ni (90.5). As for panicle number
per , Ni and Hi were higher than MR79 and MR53, although the difference is smaller than that in the previous
trait. Regarding ripened-grain percentage, Ni (88.9%) and MR53 (85.0%) were higher than MR79 (79.8%) and
Hi (79.2%). Regarding sink size (single-grain weight fertilized-spikelet number per ), they were in the same
order as in yield. The yield of MR79 (728 g/) was outstandingly high as compared with yield levels of ordinary
japonica varieties in southern Japan. This high yield was due to its more spikelets per panicle caused by Ur1, its
ripened-grain percentage being maintained at almost 80%. Moreover, MR79 had significantly higher yield than
MR53, Ni and Hi at 12 of N g/ in 2005 as well as at the three fertilizer levels in 2003. Hence, MR79 had
outstanding high yields at the low to high fertilizer levels. MR79 was 14-18 days later in 80%-heading date than
the rather late variety Hi in all cultivated conditions in the two years. MR79 was higher-yielding than the rather
early line MR53 in every environmental conditions. The lateness of MR79 might be advantageous to attain high
yield. MR79 has high eating quality comparable to that of Hi, one of high eating-quality varieties in Japan.
Consequently, MR79 could be a super-high yielding variety with exceptionally late maturity in southern Japan.

Keywords rice, Ur1 gene, spikelet number per panicle, sink size, yield

Introduction

Ur1 (Undulate rachis-1), located on chromosome 6 (Sato & Shinjyo, 1991), is an
incompletely dominant gene of rice, being characterized by undulation of primary and secondary
rachis branches. Ur1 increases not only number of secondary branches per panicle but also
spikelet number per secondary branch, resulting in a large spikelet number per panicle (Nagao et
al., 1958; Murai & Iizawa, 1994). This genic effect can increase grain yield by enlarging sink size
th
(Murai & Iizawa, 1994; Murai et al., 2002 and 2005 b). However, Ur1 decreases both ripened-grain
percentage and 1000-grain weight.
Murai et al. (2005 a) preliminarily reported that a japonica Ur1-carrying line Murai 79
(hereafter MR79) had a higher yield than the levels of ordinary japonica varieties in southern
Japan, due to its higher sink size caused by more spikelets per panicle, which was derived from the
cross of a Japanese commercial variety and an isogenic line of Taichung 65 carrying Ur1. MR79
and another Ur1-carrying line MR53 were used in the present study, which possess extremely late
and rather early heading times, respectively. The two lines, a representative variety of southern
Japan Hinohikari and a japonica high-yielding variety Nishihikari were grown under three fertilizer
levels in 2003 and two fertilizer levels in 2005. Yield, its components and other traits were
measured for the lines-varieties. On the basis of two-year data, characteristics of the two Ur1-
carrying lines were examined. We discuss utility of the lines in southern Japan.


Development of two Ur1-carrying lines
The highest-yielding F1 in the yield tests for various F1 hybrids with the Ur1 / + genotype
(Murai et al., 1997 and 2003) was used for developing recombinant inbred lines with and without
Ur1. Its maternal and paternal parents were Nishihikari and an isogenic line of Taichung 65
carrying both Ur1 and sd1-d (dee-geo-woo-gen dwarf), respectively. The F2 population was grown
in 1992, and the generation was progressed to F8 generation without selection in glasshouse
condition. In 1999, the 108 F9 lines originating from the respective 108 F2 plants were grown in a
paddy field; the two most well-ripened lines carrying Ur1, viz. MR53 and MR79 were selected from
Ur1-carrying lines by field observation. The uniformity (non-segregation) of MR53 and MR79 was
confirmed from 2000 to 2003 (F14 generation).

Field experiments
Besides MR53 and MR79, Nishihikari and Hinohikari, (denoted by Ni and Hi
respectively) were used for the field experiments. Ni is a short-culm and panicle-number type
variety possessing the highest lodging tolerance in southern Japan (Nishiyama, 1982). Hi is a
leading variety in southern Japan, which possesses rather-late heading, rather long culm, rather
many panicles.
The two Ur1-carrying lines, Ni and Hi were seeded in mid April and transplanted to a
paddy field of the faculty of Agriculture, Kochi University, Japan in early May, in the two
experimental years (Table 1). Two seedlings per hill were transplanted at a spacing of 30.0 x 15.0
cm. They were grown under three fertilizer levels (4, 8 and 16 of N g/ in total) and two fertilizer
levels (12 and 21 of N g/ in total) together with P and K elements, in 2003 and 2005, respectively
(Table 1). The randomized block design with three replications was adopted for all combinations of
the lines-varieties and fertilizer levels in each year.

Measurements of yield and other traits
All panicles of about 30 hills were sampled from each plot at maturity, and the panicle
weight of each hill was checked after cutting just at their panicle bases after air-drying. Out of nine
hills randomly selected from about 30 hills of each plot, five hills having intermediate panicle
weights were selected. The panicles in the five hills were threshed, and all spikelets in each hill
were counted. Grains after hulling (hereafter grain) were sieved at 1.7 mm to select ripened grains
by thickness. All ripened grains in each of the five hills were counted, and were weighed. The
percentage of ripened-grain weight to panicle weight in the five selected hills of each plot was
th
calculated; then, the ripened-grain weight (yield) of 30 hills of each plot was estimated from this
percentage.

Table 1. Fertilizer application, dates of sowing and transplanting for MR78, MR53, Ni and Hi in the experiments
in 2003 and 2005

Year
Total amount of fertilizer
applied (N g/m
2
)
2)

Basal dressing
(N g/m
2
)
2)

Top dressing
(N g/m
2
)
2)

2003
1)
16.0 8.0
3)
8.0
5)

8.0 4.0
4)
4.0
5)

4.0 2.0 2.0
5)

2003
2)
21.0 7.0
6)
14.0
7)

12.0 4.0 8.0
7)

1)
Dates of sowing and transplanting were April 16 and May 9 in 2003, and April 20 and May 8 in 2005.
2)
P2O5 and K2O elements were applied at the same level as N element
3)
The 6.0 g/m
2
of each nutrient element was applied with LONG
100 type, Chisso Asahi Fertilizer Co., Ltd. (about 7% of each

nutrient element is readily available) six days after transplanting. In additional to 2.0 g/m
2
of each nutrient element applied with
an ordinary chemical fertilizer before puddling.
4)
The 2.0 g/m
2
of each nutrient element was applied with LONG 100 type, in addition to 2.0 g/m
2
of each nutrient element
applied before puddling.
5)
LONG
100 type was applied on June 30 for MR53, July 27 for MR 79, July 14 for Ni (Nishihikari) and July 9 for Hi
(Hinohikari).
6)
The 3.0 g/m
2
of each nutrient element was applied with LONG
100 type six days after transplanting. In additional to 4.0 g/m

2

of each nutrient element applied with the ordinary chemical fertilizer before puddling.
7)
Another slow-release coated fertilizer, LONG
100 type, Chisso Asahi Fertilizer Co., Ltd. (about 3% of each nutrient element is
readily available) was applied on May 20 for MR53, June 2 for MR79, June 9 for Ni and June 5 for Hi.


In yield, the lines-varieties were ranked in the order MR79 > MR53 > Ni > Hi at every
fertilizer level in the two years: MR79 and MR53 were 30 to 70% and 23 to 48%, respectively,
higher than Hi in the five environments (Table 2). Regarding spikelet number per panicle, they were
in the order MR79 > (or ) MR53 > Hi > (or ) Ni at each of the fertilizer levels in the two years. In
this trait, MR79 and MR53 were 24 to 40% and 21 to 30%, respectively, higher than Hi in the five
environments. As for panicle number per m
2
, MR79, MR53 and Ni were 95-110%, 92-100% and
103-111%, respectively, of Hi in the two years, although the difference among the four lines-
varieties in this trait was smaller than that in the previous trait in every environment. In ripened-grain
percentage, Hi was around 80% and the lowest among the lines-varieties in every environment.
MR53 was similar to or not so different from Ni in every environment. MR79 was not significantly
different from Ni in all environments except at 21 of N g/m
2
in 2005. In terms of 1000-grain weight,
Ni was heavier than the other lines-variety, and either MR53 or MR79 was similar to or not so
different from Hi in both years. Regarding sink size, they were in the same order as in yield. In culm
length, MR79 was similar to Hi. MR53 was rather longer than low-height Ni in both years. They had
panicle lengths within the ranges of 2.1 and 2.5 cm in 2003 and 2005, respectively, although
varietal difference was detected. MR53 and MR79 were 11-17 days earlier and 14-18 days later,
respectively, in 80% heading date than Hi in the two years.
The higher the fertilizer level, the higher the yield in each line/variety in each year (Table
2). Similar fertilizer responses were noticed in both spikelet number per panicle and panicle number
per m
2
, although the latter trait was more responsive than the former trait in each line/variety in both
years. All line-varieties except MR53 had the lowest ripened-grain percentage at 4 of N g/m
2
in
2003, whereas they had higher values at 12 of N g/m
2
than at 21 of N g/m
2
in 2005. However, range
caused by fertilizer effect within each line/variety was less than 5.1% inclusive in each of the years.
Every line/variety had little higher 1000-grain weight at 16 of N g/m
2
than at 4 of N g/m
2
in 2003, but
such consistent response was not detected in 2005.
th
Regarding sink size (single-grain weight fertilized-spikelet number per m
2
), they were in
the same order as in yield (Table 2). The yield of MR79 at 21 of N g/m
2
in 2005 (728 g/m
2
) was
outstandingly high as compared with yield levels of ordinary japonica varieties in southern Japan.
This high yield was due to its more spikelets per panicle caused by Ur1, and its ripened-grain
percentage being maintained at almost 80%. Furthermore, MR79 had significantly higher yield than
MR53, Ni and Hi at the other four environments. Hence, the high yielding ability of MR79 was stable
over the low to high fertilizer levels.

Table 2. Yield and other traits of MR79, MR53, Ni and Hi at the three fertilizer levels in 2003 and two fertilizer
level in 2005

Trait year
Fertilizer
Level
(N g/m
2
)
MR79 MR53 Ni (Nishihikari)
Hi (Hinohi-
kari)
LSD
Yield 2003 16 673
a
(149) 612
b
(136)
2)
554
c
(123) 451
de
37
8 626
b
(165) 549
a
(145) 478
a
(126) 379
a

4 553
c
(170) 481
a
(148) 442
a
(136) 326
a

2005 21 728
a
(130) 723
a
(130) 695
a
(124) 558
a
32
12 662
c
(131) 626
a
(123) 572
a
(113) 507
a

Spikelets/
panicle
2003 16 103.8
ab
(124) 107.4
a
(128) 80.6
de
(96) 83.6
d
5.2
8 101.4
bc
(130) 101.8
bc
(130) 76.5
ef
(98) 78.3
ef

4 102.0
b
(137) 96.9
c
(130) 74.1
f
(100) 74.3
f

2005 21 132.7
a
(140) 116.0
c
(123) 90.5
de
(96) 94.5
d
6.3
12 123.8
b
(134) 111.2
c
(121) 85.2
e
(92) 92.1
d

Panicle/
m
2

2003 16 338
b
(107) 309
c
(97) 336
a
(106) 317
b
14
8 317
b
(110) 288
cd
(100) 314
b
(109) 287
cd

4 289
c
(105) 268
e
(98) 304
b
(111) 274
de

2005 21 354
bcd
(95) 360
bc
(96) 389
a
(104) 374
ab
20
12 326
ef
(96) 312
f
(92) 349
cd
(103) 339
de

Ripened
grain
percent-
tage
2003 16 94.0
ab
(115) 91.6
b
(112) 94.1
ab
(115) 82.0
c
2.7
8 95.3
a
(117) 93.0
ab
(114) 93.2
ab
(114) 81.6
cd

4 92.4
b
(117) 92.4
b
(117) 92.7
ab
(117) 78.9
d

2005 21 79.8
c
(101) 85.0
b
(107) 88.9
a
(112) 79.2
c
2.4
12 84.9
b
(104) 88,9
a
(109) 85.5
b
(105) 81.3
cb

1000-
grain
weight
1)

(g)
2003 16 20.4
cde
(98) 20.2
e
(97) 21.7
a
(105) 20.8
c
0.4
8 20.4
cde
(99) 20.2
e
(98) 21.3
b
(103) 20.6
cd

4 20.3
de
(100) 20.1
cde
(99) 21.1
b
(104) 20.3
de

2005 21 19.5
d
(97) 20.4
b
(102) 22.2
a
(111) 20.0
c
0.4
12 19.3
d
(97) 20.3
bc
(101) 22.5
a
(112) 20.0
c

Sink
size
3
)
(g/m
2
)
2003 16 695
a
(141) 640 b (130) 567 c (115) 492 de 38
8 640
b
(151) 566 c (134) 492 de (117) 422 f
4 577
c
(155) 496 d (133) 458 ef (123) 373 g
2005 21 827
a
(131) 780 b (123) 733 c (116) 631 de 32
12 726
c
(129) 659 d (117) 618 e (110) 562 f
Culm
length
(cm)
2003 16 73.5 a (97) 65.9 b (87) 63.6 c (84) 75.6 a 2.1
2005 21 77.0 a (191) 66.1 b (87) 64.6 b (85) 75.9 a 2.4
Panicle
length
(cm)
2003 16 20.3 ab (110) 19.7 b (107) 20.5 a (111) 18.4 c 0.8
2005 21 22.8 a (112) 21.6 b (106) 20.5 c (101) 20.3 c 0.9
80%-
heading
date
2003 4-16 Aug.22 July 28/29 Aug.13 Aug.9
2005 12-21 Aug.23/24 July 21 Aug.11 Aug.7
1)
Brown rice weight after sieving at 1.7mm, being adjusted into 15% moisture.
2)
Percentage to H in parentheses
3)
Single-grain
weight x fertilizer-spikelet number per m2. Values followed by the same letter within each year in a trait are not significantly
different at the 0.05 level being determined by LSD in the table.

MR79 was 14-18 days later in 80% heading date than the rather late variety Hi in all
environmental conditions in the two years. MR79 was higher-yielding than the ratherearly line
MR53 in every environmental condition. The lateness of MR79 might be advantageous to attain
th
high yield. MR79 has high eating quality comparable to that of Hi, one of excellent-taste varieties in
Japan (Murai, unpublished). Consequently, MR79 could be a super-high yielding variety with
exceptionally late maturity in southern Japan.

References

Murai, M. and M. Iizawa.1994. Effects of major genes controlling morphology of panicle in rice. Breed. Sci. 44:
247-255.
Murai, M., K. Ise, S. Sato and I. Takamure. 1997. Utility of Ur-1 for developing F
1
cultivars. In Proceedings of
the International Symposium on Two-line System Heterosis Breeding in Crops China National Hybrid
Rice Research and Development Center, Changsha, China. p. 146-151.
Murai, M., Y. Sato, A. Nagayama, N. Ishii, and S. Ihashi. 2002. Effects of a major gene Ur1 characterized by
undulation of rachis branches on yield and its related traits in rice. Breed. Sci. 52: 299-307.
Murai, M., A. Nagayama, S. Sato, H. B. KC and K. Ise. 2003. High yielding F
1
hybrid carrying Ur1 (Undulated
rachis-1) gene in japonica rice. Breed. Sci. 53: 263-269.
Murai, M., S. Malangen, K. Nakamura, Y. Fukumoto, and S. Matumura. 2005 a. High-yielding japonica rice lines
carrying Ur1 (Undulated rachis-1) gene, preliminary report. SABRAO Journal of Breeding and Genetics.
37: 51-54.
Murai, M., K. Nakamura, M. Saito, A. Nagayama and K. Ize. 2005 b. Yield increasing effect of a major gene,
Ur1(undulated rachis -1) on different genetic backgrounds in rice. Breed. Sci. 55: 279-285.
Nishiyama, H. 1982. A new rice variety Nishihikari. J. Agric. Sci. (Nogyou gijutu) 37: 125-127 (in Japnese).
Sato, S. and C. Shinjyo (1991) Genetic studies on genetic male sterile mutant obtained through breeding of
isogenic translocation line of Taichung 65 in rice, Oryza sativa L. Jpn. J. Breed. 41: 451-459.

th
Oxidative Stress and its Relation to Radiation Use Efficiency in
Rice Growing under Rainfed Condition in Northeast Thailand

Kohtaro Iseki
a,*
, Koki Homma
a
, Boonrat Jongdee
b

a
Graduate School of Agriculture, Kyoto University, Kyoto, Japan
b
Ubon Rice Research Center, Ubon Ratchathani, Thailand
* Corresponding author: Graduate School of Agriculture, Kyoto University, Sakyo-ku, 6068502, Kyoto, Japan
Tel.: +81 75 753 6042; fax: +81 75 753 6065.
[email protected]

Abstract

In rainfed cultivation of rice, the scarcity of available water often inhibits plant growth. Under such conditions, the
drought induces oxidative stress which damages to photosynthetic cells such as protein degradation, lipid
peroxidation and enzyme inactivation. In this study, we evaluate oxidative damage for 10 rice genotypes under
rainfed condition in relation to radiation use efficiency (RUE). Although the drought stress was relatively mild as
shown in the slightly decreases of stomatal conductance and leaf water potential, RUE under rainfed condition
was significantly decreased from that under flooded condition. The oxidative damages evaluated by chlorophyll
fluorescence and lipid peroxidation were also increased under rainfed condition. The genotypic variation of RUE
in both water conditions was negatively correlated to the value of midday Fv/Fm and it was thought to be
affected by the canopy structure of each genotypes. Damage of leaf cells evaluated by membrane stability index
under rainfed condition was not significantly different from that under flooded condition, but the larger
photoinhibition and lipid peroxidation seems to cause severe cell damage when the water scarcity continues for
long term.

Keywords: rice, photoinhibition, chlorophyll fluorescence, drought, oxidative stress

Introduction

Plant oxidative stress is induced by various abiotic stresses and damages to leaf cells
(Mittler, 2002). Under drought and high light conditions, decreasing of energy use for Calvin cycle
leads to over excitation of energy which causes generation of reactive oxygen species (ROS) and
promote oxidative damage to photosynthetic cells (Murata et al., 2007). Oxidation of cell membrane
increases water leakage and decreases leaf water potential. In addition, severe oxidative stress is
thought to be a cause of metabolic limitation in Calvin cycle, inducing non-stomatal inhibition of
photosynthesis (Lawlor, 2002). Drought is an increasingly important constraint of rice production:
the scarcity of water resource for agriculture provides the opportunity for rice to have water deficit
even for irrigated production as well as for rainfed production. However, the relation between
oxidative stress and drought stress has not been examined in terms of crop response under field
conditions with various environmental stresses.
To clarify the relationship between drought and oxidative stress under field condition, we
firstly focused oxidative stress of rice in relation to plant water status. Effect of the oxidative stress
on plant growth was evaluated in relation to RUE.


Field growth conditions
Ten rice genotypes from Surin1 backcross introgression lines with IR68586-FA-CA-143
(BC
3
) were used. 3 weeks seedlings were transplanted with the plant density of 25 plants m
-2
in
th
rainfed and flooded field on 12th August 2010 at Ubon Rice Research Center, Northeast Thailand.
Fertilizer was applied with 3-3-1.5 g m
-2
of N-P
2
O
5
-K
2
O for each field. The items below were
measured from 2 to 9 weeks after transplanting.

Radiation use efficiency
Total shoot dry weight was measured at 2 and 9 weeks after transplanting, and the
difference of dry weight was defined as total shoot growth. Radiation use efficiency (RUE) was
calculated as RUE (g MJ
-1
) = (total shoot growth)/(total intercepted solar radiation). To determine
canopy light absorbance rate (kc), photosynthetic active radiation (PAR) at the top and bottom of
the canopy in each plot was measured with a linear PAR intercept-meter (AccuPAR, Decagon,
USA) under diffused solar radiation conditions once every week. The weekly accumulation of
incident solar radiation was multiplied by the weekly value of kc, and summarized during the period
as total intercepted solar radiation..

Chlorophyll fluorescence, gas conductance (gs) and leaf water potential (LWP)
Maximum quantum yield (Fv/Fm) and effective quantum yield (
PS2
) of photosystem was
measured by chlorophyll fluorometer (OS-30p, Opti Science, USA) in early morning and midday of a
clear sunny day every week. The topmost fully expanded leaves were used for the measurement.
Simultaneously, gs and LWP of the topmost fully expanded leaves were also measured.

Membrane stability and lipid peroxidation
The topmost fully expanded leaves were sampled at 8 weeks after transplanting and used
for the following analyses. The leaf membrane stability index (MSI) was determined according to
Sairam and Saxena (2000). Leaf discs were soaked in distilled water at 40 C for 60 min and its
electrical conductivity recorded (C1). Subsequently the same samples were kept in boiling water for
10 min and its electrical conductivity also recorded (C2). MSI was calculated as MSI (%) = [1
(C1/C2)] 100.
The level of lipid peroxidation was measured in terms of malondialdehyde (MDA) content,
a product of lipid peroxidation. Fresh leaf sample was homogenized in 20% trichloroacetic acid
(TCA). The homogenate was centrifuged at 12000 G for 10 min. The 0.5 ml aliquot of the
supernatant was added to 1.5 ml of 0.5% thiobarbituric acid in 20% TCA. The mixture was heated
at 95C for 30 min and then quickly cooled in ice. After centrifugation at 3000 G for 10 min, the
absorbance of the supernatant was measured at 532 nm. The value for non-specific absorption at
600 nm was subtracted. The MDA content was calculated using its extinction coefficient of 155mM
-1

cm
-1
and expressed as nmol MDA g
-1
fresh weight.


Most genotypes decreased their total shoot growth under rainfed condition from that under
flooded condition. The smaller shoot growth under rainfed condition was mainly caused by the lower
RUE (Figure 1). The Surin1 which showed higher RUE under flooded condition also showed higher
RUE under rainfed condition. Another parent line, IR68586-FA-CA-143 showed lower RUE under
both water conditions (Table 1). However, except these two parent genotypes, the relationship of
RUE between rainfed and flooded condition was not obvious. It implies that the effect of water
limitation on RUE was different among genotypes. In the theory, RUE can be explained as the
function of canopy photosynthesis (Sinclair and Horie, 1989, Reynolds et al., 2000). In terms of
single leaf, photosynthetic rate is closely related with stomatal conductance, which is governed by
LWP (Medrano et al., 2002). The slightly but significantly lower value of gs and LWP under rainfed
condition suggested that mild drought stress was occurred (Table 1). The drought stress might
decrease RUE.
th
200
300
400
500
600
200 250 300 350 400
T
o
t
a
l

s
h
o
o
t

g
r
o
w
t
h

(
g

m
-
2
)
Total Intercepted radiation (MJ m
-2
)
RUE=1.0
RUE=1.5
RUE=2.0

Figure 1. Genotypic variation in total shoot growth, total intercepted solar radiation and RUE under rainfed and
flooded conditions. Open circle and closed diamond represents the genotype grown under flooded and
rainfed condition, respectively. Data are average of three replicates.

Table 1. Radiation use efficiency, stomatal conductance and leaf water potential of 10 genotypes under flooded
and rainfed conditions

RUE (g MJ
-1
) g
s
(mmol m
-2
) LWP (Mpa)

Flooded Rained Flooded Rained Flooded Rained
IR68586-FA-CA-143 1.42 0.97 218 184 -0.796 -0.836
Surin 1 1.83 1.34 214 224 -0.797 -0.864
IRUBN030055-5-87 1.38 1.43 239 244 -0.808 -0.906
IRUBN030055-5-112 1.73 1.17 261 192 -0.808 -0.856
IRUBN030055-5-190 1.68 1.25 286 230 -0.819 -0.853
IRUBN030056-10-42 1.49 1.32 280 220 -0.789 -0.850
IRUBN030056-10-107 1.65 1.32 229 189 -0.822 -0.847
IRUBN030062-1-9 1.68 1.20 249 222 -0.806 -0.864
IRUBN030063-9-4 1.33 1.14 311 229 -0.847 -0.847
IRUBN030070-9-32 1.66 1.09 229 194 -0.861 -0.861
Average 1.59 1.22 252 213 -0.803 -0.858
Genotype (G) * ns ns
Water condition (E) *** *** ***
G x E * ns ns
Data are average of three replicates. * and ** represent statistically significant at 0.05, 0.01 level, and ns represents not
significant.

The water limitation, even mild drought, decreases carbon fixation of rice and induces
oxidative damage (Zhou et al., 2007). Measurement of chlorophyll fluorescence can easily evaluate
photosynthetic capacity, and is widely applied for environmental stresses studies. The maximum
quantum yield of photosystem (Fv/Fm) is an indicator of photoinhibition which relate to oxidative
stress (Maxwell and Johnson, 2000). Generally, Fv/Fm decreases with increasing of exposed light
intensity at midday. Decrease in Fv/Fm by high PAR was larger under rainfed condition than that
under flooded condition (Figure 2). The same tendency was observed for the effective quantum
yield (
PS2
) but the difference was not significant between rainfed and flooded conditions. It is
known that the carbon fixation rate is closely related to the value of
PS2
under the environment of
constant CO
2
concentration (Kato et al., 2003). Decrease of
PS2
induces over reduction in electron
transport chain and increases oxidative damage. The lower value of Fv/Fm under rainfed condition
is thought to be resulted by increased oxidative damage that derived from inhibition of carbon
fixation. The genotypic variation in Fv/Fm and
PS2
was not significant, because of large residual
variation in this study.

th
0.60
0.65
0.70
0.75
0.80
0.85
0 500 1000 1500
F
v
/
F
m
PAR (mol m
-2
s
-1
)
0.0
0.2
0.4
0.6
0 500 1000 1500
P
S
2
PAR (mol m
-2
s
-1
)

Open circle and closed diamond represents the genotype grown under flooded and rainfed condition, respectively. Data are
average of four replicates.

Figure 2. Decrease of Fv/Fm and
PS2
with increasing of PAR in midday. Fv/Fm was measured in early morning
and midday, and
PS2
was measured only in midday.

MDA content was higher under rainfed condition, indicating that damage of cell membrane
by reactive oxygen species was larger under rainfed than that under flooded condition (Table 2). On
the other hands, difference of MSI, another indicator of membrane damage, was not significant
between the two water conditions. MDA is a product of lipid of peroxidation, while MSI indicates
water leakage from cell induced by oxidative damage to cell membrane (Mittler, 2002). Accordingly,
the result in this study may suggest that lipid peroxidation proceeded under rainfed condition but the
damage was alleviated by antioxidation mechanisms.

Table 2 Malondialdehyde content and membrane stability index of 10 genotypes under flooded and rainfed
conditions

MDA (nmol g
-1
f.w.) MSI (%)
Flooded Rainfed Flooded Rainfed
IR68586-FA-CA-143 88.4 107.3 81.7 76.1
Surin 1 88.3 93.5 81.5 76.2
IRUBN030055-5-87 67.7 151.9 79.7 78.6
IRUBN030055-5-112 70.2 78.4 77.8 75.7
IRUBN030055-5-190 85.5 109.3 75.7 77.1
IRUBN030056-10-42 73.1 57.2 79.6 76.0
IRUBN030056-10-107 75.3 58.0 78.5 79.0
IRUBN030062-1-9 44.2 102.0 82.3 80.7
IRUBN030063-9-4 88.1 97.8 83.1 78.1
IRUBN030070-9-32 89.6 114.5 76.5 80.0
Average 77.0 97.0 79.7 77.7
Genotype (G) *** ns
Water condition (E) *** ns
G x E *** ns
Data are average of three replicates. * and ** represent statistically significant at 0.05, 0.01 level, and ns represents not
significant.

Drought stress decreases RUE and Fv/Fm, implying the RUE was positively correlated
with Fv/Fm. However, the relationships for each water condition showed negative correlations
(Figure 3). This suggests that the genotypes which showed larger canopy photosynthesis were
suffered with larger photoinhibition. Because RUE is not determined only by single leaf
th
photosynthesis but also canopy structure, further study is necessary to reveal the effect of
photoinhibition on plant production.

0.5
1.0
1.5
2.0
0.70 0.72 0.74 0.76
R
U
E

(
g

M
J
-
1
)
Fv/Fm
0.5
1.0
1.5
2.0
0 50 100 150 200
R
U
E

(
g

M
J
-
1
)
MDA content (nmol g
-1
f.w.)

Open circle and closed diamond represents the genotype grown under flooded and rainfed condition, respectively. Fv/Fm is the
average of three measurement days from sixth to eighth weeks after transplanting.

Figure 3. Relationships of RUE to Fv/Fm and to MDA content.

In this study, oxidative stress in rice was evaluated under field environment of rainfed
condition during wet season where drought stress was relatively mild. The drought stress
decreased RUE and, increased photoinhibition and lipid peroxidation. The results suggest that the
oxidative stress was associated with dry matter production. To elucidate the relation between
drought and oxidative stress and to apply it for breeding program of drought tolerance, further
studies are necessary.

References

Kato MC, K Hikosaka, N Hirotsu, A Makino and T Hirose. 2003. The excess light energy that is neither utilized in
photosynthesis nor dissipated by photoprotective mechanisms determines the rate of photoinactivation in
photosystem II. Plant Cell Physiol. 44:318-325.
Lawlor DW. 2002. Limitation to photosynthesis in water-stressed leaves: stomata vs. metabolism and the role of
ATP. Ann. Bot. 89:871-885.
Maxwell K and GN Johnson. 2000. Chlorophyll fluorescence--a practical guide. J. Exp. Bot. 51:659-668.
Medrano H, JM Escalona, J Bota, J Gulias and J Flexas. 2002. Regulation of photosynthesis of C3 plants in
response to progressive drought: stomatal conductance as a reference parameter. Ann. Bot. 89:895-
905.
Mittler R. 2002. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 7:405-410.
Murata N, S Takahashi, Y Nishiyama, and SI Allakhverdievd. 2007. Photoinhibition of photosystem II under
environmental stress. Biochim. Biophys. Acta 1767: 414-421.
Reynolds MP, M Ginkel and JM Ribaut. 2000. Avenues for genetic modification of radiation use efficiency in
wheat. J. Exp. Bot. 51:459-473.
Sairam RK and DC Saxena. 2000. Oxidayive stress and antioxidant in wheat genotypes: possible mechanism of
water stress tolerance. J. Agron. Crop Sci. 184:55-61.
Sinclair TR and T Horie. 1989. Leaf nitorogen, photosynthesis and crop radiation use efficiency: a review. Crop
Sci. 29:90-98
Zhou Y, HM Lam and J Zhang.et al. 2007. Inhibition of photosynthesis and energy dissipation induced by water
and high light stresses in rice. J. Exp. Bot. 58:1207-1217.

th
The Growth Characteristics of Some Varieties of Acehs Local Rice
(Oriza sativa L.) on Acid Soils

Elly Kesumawati
a,*
, Erita Hayati
a
, Muhafaz Zulusfitri
a

Faculty of Agriculture Department of Agrotechnology, Syiah Kuala University
Banda Aceh, Aceh Province, Indonesia
* Corresponding author: Faculty of Agriculture Jl.Tgk.Hasan Krueng Kalee, Kopelma Darussalam,
Banda Aceh 23111, Aceh Province, Indonesia
Tel.: +0651-7552223; fax: +065-17555269
[email protected]

Abstract

To identify the agronomic and morphological characteristic of some local rice varieties in Aceh, to describe
based on the classifications of rice and to observe the varieties resistant to soil acidity, it was needed to conduct
a study of 18 Acehs local rice varieties and one Dupa variety as a comparison. The results showed that there
were 6 local varieties of Aceh tolerant to Al toxicity and 12 were somewhat tolerant varieties, as well as varieties
had tolerant nature to Dupa. There were differences in flowering age, counted from planting rice to grew
panicle by 10%. This age difference could be grouped into three, namely: age of flowering under 100 days was
found in 2 varieties, age of flowering ranged from 100 to 119 days was found in 12 varieties (including Dupa),
while flowering more than 120 days was found in 5 varieties. There were 15 varieties of rice belonging to the
class Indica and 4 varieties in Javanica group. The largest stem diameter by Sigupai Wangi variety and smallest
by Pade Cut Kresek variety. Longest panicle varieties belonged to Pade Rangan and shortest Sigupai Nagan
Raya. There were 14 varieties which did not possess grain hair-tip, while shortest grain hair-tip by 4 varieties
and 1 varieties of grain had long hair-tip. The widest seed variety was found in Dupa and the smallest was from
Pade Cut Kresek. The thick seed was Dupa variety and the thinnest was Ramos Tihion. Based on length, the
longest seed character was found in 17 varieties and other 2 variety was just long.

Keywords: characteristics, variety, local Acehs rice, acid soils

Introduction

Rice is a strategic commodity plays an important role in the economy and national food
security and become a major base in the revitalization of agriculture in the future. About 95% of
national rice production depends on the production of rice paddies and only 5% of upland rice.
Increased productivity of rice reached only 0.40% per year while the land use field reaches 0.77%
per year (Puslitbangtan, 2007).
Expansion of the current wetland is difficult because suitable land for new rice fields are
very limited, the cost of irrigation system development and printing of new rice fields are very
expensive. Alternative increase rice production can be done by the expansion of upland rice
cropping on dry land. Dry land area reached 54.4 million ha, but the 45.8 million ha of land of which
is acid (BPS, 2007), and 11 million hectares more of them has the potential to be developed as
upland rice cropping land (Puslitbangtan, 2007). However, the development of upland rice on dry
land faced with the problem of Al toxicity and nutrient deficiency phosphate appearing
simultaneously on acid soils of land (Kochian et al., 2004). Liming and P fertilization are used to
overcome these problems, but this way is not economical for areas that are far from sources of
lime, not a good means of transportation, the availability of P fertilizers is often not continuous and
expensive. It would require the development of varieties that grace Al and efficient in the use of P.
Aceh is a province in Indonesia rich in diversity of rice local varieties, which needs to be
preserved and utilized for sustainable development in order to improve the welfare of all people.
th
Characterization of genetic resources will provide added value in enriching the "gene pool", the new
diversity of local varieties is useful for the assembly of new varieties (Neereja et al., 2005). These
genetic resources continue to decline due to lack of attention, their utilization, and the changes in
traditional farming practices. Introduction of high yielding varieties called genjah to rice production
centers in various regions may cause genetic erosion of local varieties existing in certain areas
(Mishra et al., 2009). The existence of genetic erosion due to modern farming practices led to
increasingly felt the importance of germplasm collection and conservation. To anticipate the erosion
of plant genes, it is necessary to preserve the plant genetic material through exploration,
characterization, and documentation (Hanarida et al., 2005). Genetic diversity can be determined
through characterization and identification. Improved varieties can be done either through
conventional breeding or modern breeding program utilizing biotechnology assemblies germplasm
using seeds from existing genetic resources. Each variety has certain important characteristics
which can be used for crossing among varieties (Liu et al., 2007). Aceh local rice varieties are still
widely used by farmers in many districts in Aceh, but in relatively small quantities. Until now, local
rice germplasm has not been characterized and evaluated, therefore, this requires the identification,
conservation and classification which are useful for the in breeding programs and serve for the
protection of local plant varieties (Menkumham, 2000; Bhuyan et al. 2007; Silitonga, 2008).
This study aimed to identify the agronomic properties and morphology of 18 local rice
varieties in Aceh, based on the classification of rice varieties and to observe their resistant to soil
acidity.


The research was conducted at the Garden Experiments Faculty of Agriculture, University
of Syiah Kuala Banda Aceh from January to June 2010. Rice seeds were 18 local varieties
(varieties Ramos Merah, Rom Mokot, Sigupai Wangi, Sigupai Nagan Raya, Sambei, Rasi Singke,
Kepala Gajah Kinco, Bo Padang, Rasi Kuneng, Pade Mangat Bu, Bo Santeut, Ramos Tihion, Pade
Cut Kresek, Pade Pineung, Cantek Puteh, Itam Tangke, Pade Rangan, Sigupai Blang Pidie),
obtained from farmers from several districts of Aceh, and a control varieties of varieties of Incense
originally from stone Estuary Borneo leaf blast-resistant and tolerant to Al toxicity.
The research was conducted using a randomized block design (RGD), non-factorial with 3
replicates. Treatment of rice varieties (V) consisted of 19 varieties, and 57 units experiment. Each
experimental unit consisted of four plants, so that overall there were 228 units observation. Soils
used were soil type ultisol (pH 4.35) at 950 kg obtained from Jantho Aceh Besar district. The soil
weight was 8 kg/bucket. Fertilizers used were Urea, KCl, and SP 36 at 2 kg of each. Seeds were
germination on paper soaked in water to thei field capacity, then left for 5 days. Each bucket
consisted of four seedlings of rice plants. A seeding was planted in each planting hole. Furadan at
0.5 g/bucket was applied to soil surface in each bucket. Urea, SP 36 and KCl at 1 g / bucket of each
were given one day before planting. At 15 DAT urea at 1 g/bucket were applied, at 45 DAT Urea
and KCl were again applied at 1 g / bucket. At 55 DAT Urea applied at 1 g/bucket. Plant
maintenance is carried out by watering, weeding, as well as controlling pest and disease.
The characters observed were agronomic trait (plant height and number of tillers per hill at
the age of 30, 45 and 60 DAT, level of tolerance, and the age of flowering) and morphology
(diameter of the stem segment below, panicle length, feather edge grain, seed width, seed
thickness, and length of seed). The data were described based on Characterization and Evaluation
System Guide Rice with scoring for each character observed (Deptan, 2003). Data were calculated
for the relative values (RV) to determine differences in plant height and number of tillers of the soil
acidity. Grouping level of tolerance to soil acidity was based on the criteria modified from Sarkarung
(1986) then grouped to tolerant (when the value of RV was greater than 75%), somewhat tolerant
th
(when the value of RV was between 50 to 74%), sensitive (when the value of RV was less than
50%).
The relative value (RV) (%) = Plant height or number of pups at acid conditions x 100%
Plant height or number of pups at normal conditions


Agronomic characteristic
The results showed that rice varieties significantly affected the relative values for plant
height at 30 DAT, but not at 45 and 60 DAT (data not showed). The relative value of number of
tillers per hill of rice plants was not significantly different at 30, 45, and 60 DAT (data not showed).
The Aceh local rice varieties Sigupai Nagan Raya (V4) and Cantek Manis (V15) were taller than
other local varieties such as Dupa (V19) variety. The shortest rice plant varieties was Red Ramos
(V1). The plants high in rice plants had a positive and negative values on the cultivation system.
The tall rice plants can be used as an elder male in producing hybrid seed. Tall rice plants will be
more easily to spread its pollen to the shorter one (female elders). Hybrid rice production needa the
stud taller than 20 cm for the elder females. However, tall rice plants are susceptible to fall down
(Samac and Tasfaye, 2003).
Grouping of local rice varieties tolerant to acid soil in Aceh was based on the relative value
(RV). According to Sarkarung (1986), local rice in Aceh produces 6 varieties having a relative value
of more than 75% (tolerance type), and 12 varieties having a relative value between 50-74%
(somewhat tolerant type) similar to the control Dupa tolerant nature (Table 1). Varieties tolerant to
high acid soil may also tolerant to stress of Al. This was shown by the relative value of more than
75%. Tolerant plants allegedly had the ability to suppress the adverse influence of Al by reducing
the Al
3+
ion uptake by roots and neutralize toxic Al in the network, so that plant growth is not
disturbed (Watanabe and Osaki, 2002; Sopandie et al., 2003). Variations in the nature of resistance
18 local varieties of Aceh on Al toxicity in this study presumably because the genes resistant to Al
toxicity did not work together (Nguyen et al., 2002).
Age of flowering plants in Aceh local rice was varied. Sambei (V5) and Rom Mokot
varieties (V2) were flowering under 100 days. Varieties flowerring at 100-119 days were 11
varieties, including control variety Dupa (V19), varieties flowerring at more than 120 days were 5
varieties (Table 1).

Morphological characteristic
The results showed that local rice varieties based on morphological characters of rice were
grouped in two, namely the Indica and Javanica groups. There were 15 varieties Indica type, and 4
varieties of Javanica. Indica rice (paddy cere) had several characteristics of : having a lot of roots,
smooth leaf surfaces, long panicle, litle hair on the the surface of the grain, no tail on the end grain,
slender grain shape, grain size was small to moderate and harvest age was faster. Characteristics
of the group Javanica rice (paddy fur) were : the number of tillers was less, leaves had a rough
surface, long panicle, hairy grain surface, a tail on the end grain, medium to large grain size and the
age old crop (Grubben and Partohardjono, 1996).
The largest diameter stem segment was found in Sigupai Wangi (V3), while the smallest
diameter of the rod segment was found in Pade Cut Kresek variety (V13) (Table 2). The longest
panicle variety was found in Pade Rangan (V17) and the shortest panicle variety was found in
Nagan Raya Sigupai (V4) (Table 2). According to the AAK (1990), panicle length is divided into
three different sizes which are short panicle (less than 20 cm), medium panicle (20-30 cm), and
long panicle (more than 30 cm).
th
Table 1. Grouping of local rice varieties for tolerance to soil acidity based on the relative value (NL) and by age
of flowering

Varieties of rice
Relative value
(%)
Criteria
Flowers
age
V1 (Ramos Merah)
V2 (Rom Mokot)
V3 (Sigupai Wangi)
V4 (Sigupai Nagan Raya)
V5 (Sambei)
V6 (Rasi Singke)
V7 (Kepala Gajah Kinco)
V8 (Bo Padang)
V9 (Rasi Kuneng)
V10 (Pade Mangat Bu)
V11 (Bo Santeut)
V12 (Ramos Tihion)
V13 (Pade Cut Kresek)
V14 (Pade Pineung)
V15 (Cantek Puteh)
V 16 (Itam Tangke)
V17 (Pade Rangan)
V18 (Sigupai Blang Pidie)
V 19 (Dupa)
66,40
75,52
65,71
79,53
72,75
68,09
72,44
77,37
68,69
73,43
74,98
73,03
69,19
77,00
75,23
75,06
65,54
70,71
77,21
somewhat tolerant
Tolerant
somewhat tolerant
Tolerant
somewhat tolerant
somewhat tolerant
somewhat tolerant
Tolerant
somewhat tolerant
somewhat tolerant
somewhat tolerant
somewhat tolerant
somewhat tolerant
Tolerant
Tolerant
Tolerant
somewhat tolerant
somewhat tolerant
Tolerant
113
98
112
112
96
120
130
130
130
120
101
112
115
110
101
119
115
116
100

Table 2. Classification of rice based on morphological characters, diameter of rod segment and panicle length of
rice plants

Varieties of rice Group
Diameter of rod
segments (cm)
Length of
panicle (cm)
V1 (Ramos Merah)
V2 (Rom Mokot)
V3 (Sigupai Wangi)
V5 (Sambei)
V6 (Rasi Singke)
V8 (Bo Padang)
V9 (Rasi Kuneng)
V11 (Bo Santeut)
V12 (Ramos Tihion)
V14 (Pade Pineung)
V15 (Cantek Puteh)
V 16 (Itam Tangke)
V17 (Pade Rangan)
V 19 (Dupa)
Indica
Indica
Indica
Indica
Indica
Indica
Indica
Javanica
Javanica
Indica
Javanica
Indica
Indica
Indica
Indica
Javanica
Indica
Indica
Indica
0.51
0.53
0.91
0.58
0.55
0.55
0.59
0.61
0.70
0.43
0.52
0.61
0.42
0.53
0.50
0.54
0.60
0.50
0.60
24.03
23.50
20.65
18.85
23.28
29.70
24.03
24.23
30.17
24.63
28.85
26.50
21.75
29.65
24.50
20.18
34.88
23.78
21.68

Grain hair-tip was not found in 13 local rice varieties and the control Dupa (V19). Four
varieties had short grain hair-tip and some furry at Rasi Singke (V6), Bo Padang (V8), Rasi Kuneng
(V9) and Itam Tangke (V16), while Bo santeut (V11) varieties had a long grain hair-tip and all furry
(Table 3).
th
Differences in width and thickness of seeds in each variety are presented in Table 3.
Control varieties (V19) had the widest seed, meanwhile the Pade Cut Kresek varieties (V13) was
the slimmest variety. Varieties of Dupa (V19) also had the thickest seeds and variety Ramos Tihion
(V12) was a thin variety. Character of the length scale 1 (seed longer than 7:50 mm) was found at
17 varieties, including varieties of Dupa (V19). Character length scale 2, (seed length of 6.61-7.50
mm) was found in Singke Rasi variety (V6) and Itam Tangke (V16).
A number of rice varieties characteristic were difficult to distinguish. Abdullah et al., (2006)
stated that the differences will affect the nature of plant varieties. Each plant has the characteristics
for special properties that may differ from each other, so it will show the diversity of characters.
According to Lesmana et al., (2004) morphological features often used to distinguish varieties of
rice are plant height, stem color, leaf color, leaf surfaces, grain shape, grain color and grain
surfaces. The character of grain morphology on the presence of feathers covering the tip of grain,
seed thickness, seed width and seed length. According Aldair et al., (1966) in Grist (1986), grain
shape consisting of three kinds, namely rounded, medium and lean. In addition, the inflorescence
characters can distinguish rice varieties (Wet et al., 1986).

Table 3. The presence of feather tip of grain, seeds character width, thickness and length of seed grain Aceh
local

Varieties of rice
The presence of grain
hair- tip
Width seeds
(mm)
The thickness
of the seeds
(mm)
Length of
seeds
V1 (Ramos Merah)
V2 (Rom Mokot)
V3 (Sigupai Wangi)
V5 (Sambei)
V6 (Rasi Singke)
V8 (Bo Padang)
V9 (Rasi Kuneng)
V11 (Bo Santeut)
V12 (Ramos Tihion)
V14 (Pade Pineung)
V15 (Cantek Puteh)
V 16 (Itam Tangke)
V17 (Pade Rangan)
V 19 (Dupa)
Lint
Lint
Lint
Lint
Lint
Short and partly feathered
Lint
Lint
Length and all hairy
Lint
Lint
Lint
Lint
Lint
Lint
Lint
2.10
3.00
2.10
2.10
2.70
2.49
3.04
2.15
2.70
2.15
2.10
2.06
1.90
2.90
2.50
2.20
4.10
2.20
4.50
1.50
2.00
1.90
1.90
2.00
1.79
2.00
1.68
2.00
1.92
2.00
1.50
1.52
2.00
1.90
1.79
2.00
1.88
2.10
Very long
Very long
Very long
Very long
Very long
Long
Very long
Very long
Very long
Very long
Very long
Very long
Very long
Very long
Very long
Long
Very long
Very long
Very long

Acknowledgement

This work was supported by the Excellent Research of National Strategic (2009), the Ministry of
National Education Indonesia.

References

Abdullah B., R. Mudjisihono., Prajitno. 2006. Some rice genotypes towards improved quality of rice. Researcher
center for rice, Sukamandi. 5 page.
AAK . 1990. Rice cultivation. Kanisius. Yogyakarta. 172 page.
th
[BPS] Central bureau of statistics. 2007. Statistics Indonesia 2005/2006. Biro Pusat Statistik, Jakarta.
Bhuyan N., N.Basanta., K.Borah., R.N.Sarma. 2007. Genetik diversity analysis in traditional lowland rice (Oryza
sativa L.) of assam using RAPD and ISSR markers. Current Science. 93 (7): 976-972.
[Deptan] Departemen Pertanian. 2003. Guidelines characteristics and evaluation system for rice. National
Commission Germplasm. Agency for Agricultural Research and Development. 57 page.
Grist D.H. 1986. Rice (Tropical agriculture series). Sixth Edition. London : Longman Inc.
Grubben G.J.H., S.Partohardjono. 1996. Plant resources of South-East Asia No. 10: Cereals. Bogor: Prosea.
Hanarida I.S., M.Hasanah., S.Adisoemarto., M.Thohari., A.Nurhadi., I.N.Orbani. 2005. Series know your food
plant germplasm. Germplasm National Commission, Bogor. 34 page.
Kochian L.V., O.A.Heokenga., M.A.Pineros. 2004. How do crop plants tolerate acid soils. Mechanisms of
aluminium tolerance and phosphorous efficiency. Annu Rev Plant Biol 55 : 459-493.
Liu Q.L., X.H.Xu., X.L.Ren., H.W.Fu., D.X.Wu., Q.Y.Shu. 2007. Generation and characterization of low phytic
acid germplasm in rice (Oryza sativa L.). Theor. Appl. Genet. 114:803-814.
Lesmana O.S., H.M.Toha., I.Las., B.Suprihatno. 2004. Description of a new rice variety superior. Sukamandi,
Subang: Agency for Agricultural Research and Development - Research Institute for Rice.
[Menhumkam] Minister of Justice and Human Rights Republic of Indonesia 2000. Laws of the Republic of
Indonesia number 29 Year 2000 on the protection of plant varieties.
Mishra B., R.K.Sing., D.Senadhira. 2009. Enhancing genetic resources and breeding for problem soil.
http://www.idrc.ca/en/ev-85296-201-1-DO_Topic.html [14 Febuari 2009].
Neereja C.N., A.S.Hariprasad., S.Malathi., E.A.Siddiq. 2005. Characterization of tall landraces of rice (Oryza
sativa L.) using gene-derived simple sequence repeats. Current Science. 88 (1): 149-152.
Nguyen V.T., B.D.Nguyen., S.Sarkarung., C.Martinez., A.H.Paterson., H.T. Nguyen. 2002. Mapping of genes
controlling aluminum tolerance in rice: Comparison of different genetic backgrounds. Mol Genet
Genomics. 267:772 780.
[Puslitbangtan] Center for Food Crops Research and Development. 2007. Annual Report 2006 Food crops
research and development. Jakarta: National Agricultural Research and Developmen
Samac D.A., M.Tasfaye. 2003. Plan Improvement for tolerance to aluminium in acid soils. Plant Cell Tissue and
Organ Culture 75: 189-207
Silitonga T.S. 2008. Genetic resources conservation and development for rice farmers welfare. Paper presented
on the day of Rice Culture on Subang West Java.
Sarkarung S. 1986. Screening upland rice for aluminium tolerance and blast resistance. Proceedings of the
1985 Jakarta Conference. IRRI. Philipphines. pp:271-281.
Sopandie, D., I.Marzuki., M. Jusuf. 2003. Alumunium tolerance in soybean: protein profiles and accumulation of
in roots. Hayati 10 (1):30-33.
Watanabe, T., M. Osaki. 2002. Mechanisms of adaptation to high alumunium conduction in native plant species
growing in acid soil. Communication Soil Science Plant Analysis 33:1247-1260.
Wet J.M.J.D., J.R.Harlan., D.E.Brink. 1986. Reality of infraspecific taxonomic units in domesticated cereals in
styles, B. T. (ed). Infraspecific Classification of Wild and Cultivated Plants. New York: Oxford University
Press. pp: 210-222.

th
Effect of NPK Fertilizer and Biochar Applications on
Growth and Yield of Irrigation Rice

Zaitun
a*
, Khairun Nisa
b
, Sufardi
a
, Chairunas
c
, Anischan Gani
d
, Peter Slavich
e
, Malem
McLeod
e

a
Agriculture Faculty, Syiah Kuala University, Banda Aceh, Indonesia
b
Agency Implementation of Extension and Food Security of West Aceh, Indonesia
c
Provincial Agricultural Service (BPTP NAD), Banda Aceh, Indonesia
d
Indonesian Centre for Rice Research, Sukamandi, West Java, Indonesia
e
New South Wales Primary Industries, Australia
* Corresponding author: Agriculture Faculty, Syiah Kuala University, Darussalam,
Banda Aceh, Indonesia 23111.
Tel.: +62 81360301372; fax: +62 651 7555214
[email protected]

ABSTRACT

The objective of experiment was to investigate the effect of NPK and Biochar applications on paddy rice growth
and its production. The research was conducted at Empetrieng village, Aceh Besar district, Aceh Province,
Indonesia. The experimental was arranged in a randomized complete block design with two factors and four
replicates. First factor was NPK at ratio of 15:15:15 as fertilizer application (0; 60; and 120 kg ha
-1
, respectively)
and second factor was Biochar application at 0 and and 10 ton ha
-1
). The results showed that the application of
Biochar affected significanly on plant height at 28 and 90 DAP (day after planting), percentage of unfilled grain
per peanicle; whereas aplication of NPK affected significanly on plant height at 45 and 90 DAP, number of tiller
45 DAP, number of peanicle per clump, number of total grain per peanicle, number of filled grain per peanicle,
and yield ton per ha, respectively.

Keywords : NPK fertilizer, Biochar, paddy rice

Introduction

Rice is the main food of Indonesian people. The rice field has dominant contribution in
yield of paddy rice because generally rice paddy is planted in wet land. Irrigation is very important
for the rice field paddy because this influences the yield of paddy rice productivity (Adiratma, 2004).
Biochar or charcoal represents one option to soil management. Biochar had been applied
traditionally by some farmers at many places. Several reports showed that biochar has the role in
improving fertility soil. Biochar has a lot of pores because it has large surface, so it has high water
holding capacity. Although biochar is not fertilizer, it can be used as mixed fertilizers (Gani, 2009).


The field experiment was established at Empetring Village, Darul Kamal Subdistrict, Aceh
Besar District, Aceh Province, Indonesia on December 2009 to May 2010.
This research was designed as experiment field continued in laboratory with the the
following step: (a) field trial was done by planting Ciherang varietas paddy rice. NPK fertilizer and
biochar treatment were applied as according to each plot combination treatment; (b) observation
was done by looking at the plant growth i.e. plant height, and number of tiller; (c) paddy rice growth
was measured by determining the plant height at 28, 35, 45 and 90 day after planting (DAP) and
number of tiller 28, 35, and 45 day after planting (DAP). Measurement of final plant height and
number of tiller were done, at 1-2 days before harvest paddy rice; and (d) estimation to yield
component of paddy rice was done by determining the number of panicle per clump, number of total
th
grain per panicle, percentage of unfilled grain per panicle, number of filled grain per panicle, weight
of 1.000 grain at water content 14%, and yield ton per hectare at water content 14%.
The experiment was arranged in a randomized complete block design with two factors and
four replicates. First factor was NPK at 15:15:15 fertilizer application. F0 was without fertilizer;
F1was 60 kg ha
-1
NPK which was equal to 150 g plot
-1
; and F2 was 120 kg ha
-1
NPK which was
equal to 300 g plot
-1
. Second factor was Biochar application; B0 was without biochar; and B1 was
10 ton ha
-1
which was equal to 25 kg plot
-1
.


Plant Height and Number of Tiller of Paddy Rice Plant
Vegetative growth with parameter of plant height and tiller number were not significantly
affected by biochar and NPK treatments (Tables 1 and 2), eventhough, plant height and tiller
number tend to increase with biochar 10 ton ha
-1
and NPK 120 kg ha
-1
treatments. Biochar and
NPK applications can improve soil fertility by repairing soil chemical properties in the form of content
improvement and in the N, P, K nutrient availibility. Improvement of N, P, K nutrient availibility would
affect the nutrient availibility, so that can this would improve the growth of plant height and tiller
number.

Table 1. Average of plant height effect biochar and NPK treatment

Treatment
Combination
Plant height (cm)
28 DAP 35 DAP 45 DAP 90 DAP
B0 F0 42,70 a A 52,40 a A 66,45 a A 69,88 a A
B0 F1 44,45 a A 55,09 a A 71,30 a A 71,18 a A
B0 F2 43,68 a A 54,85 a A 71,73 a A 74,80 a A
B1 F0 45,23 a A 45,27 a A 65,63 a A 71,05 a A
B1 F1 46,28 a A 48,35 a A 72,80 a A 76,93 a A
B1 F2 46,75 a A 48,74 a A 76,88 a A 78,23 a A
BNT 0,05 3,206 15,341 4,627 5,700

Tabel 2. Average of tiller number effect biochar and NPK treatment

Treatment
Combination
Number of tiller (bar)
28 DAP 35 DAP 45 DAP
B0 F0 14,08 a A 12,70 a A 11,98 a A
B0 F1 12,50 a A 13,05 a A 13,68 a A
B0 F2 14,35 a A 14,53 a A 16,23 a A
B1 F0 13,05 a A 13,05 a A 11,65 a A
B1 F1 13,70 a A 15,03 a A 14,83 a A
B1 F2 14,15 a A 14,83 a A 17,18 a A
BNT 0,05
1,802 2,269 1,937

th
Mori and Marjenah (1993) reported that biochar or husk chrocoal can be used as soil
material repairing with increasing air permeability as well as the water percolation. Purnomo (2009)
stated that paddy rice plant responded to single NPK and compound NPK. Compound NPK
fertization significantly improves paddy rice plant height at the primordial stage. Improvement of this
growth is caused of by soil chemical properties may increase the rate of N and P in soil.
Kaderi (2004) stated that number of tiller per clump was higher after the addition of NPK
compared to control plant. This showed that compound of NPK added the nutrient element for plant.
Growth of tiller number is related to N sufficiency and efficacy to primordial forming.

Yield of Paddy Rice Plant
Yield component of paddy rice plant did not significantly effected either by Biochar or NPK
treatments (Table 3), eventhough the yield component of paddy rice plant tend to increase with the
application of Biochar at 10 ton ha
-1
and NPK at 120 kg ha
-1
compared to the control
treatmentwithout Biochar and without NPK.

Tabel 3. Average of yield component effect biochar and NPK treatment

Variable
Treatment combination
BNT
0,05
B0 F0 B0 F1 B0 F2 B1 F0 B1 F1 B1 F2
Number of panicle per clump
(panicle)
9,67
Aa

11,04
aA

12,54
aA

9,56
aA

10,96
aA

11,75
aA

1,249

Number of total grain per panicle
(grain)

146,72
aA

130,75
aA

117,09
aA

145,14
aA

126,61
aA

122,65
aA

20,425

Percentage of unfilled grain per
panicle (%)
20,37
aA

22,84
aA

23,14
aA

16,68
aA

19,11
aA

17,86
aA

4,569

Number of filled grain per panicle
(grain)

116,29
aA

100,81
aA

89,78
aA

120,61
aA

102,44
aA

100,63
aA

14,190

Weight of 1.000 grain at water
content 14% (gram)

24,78
aA

24,93
aA

24,74
aA

25,02
aA

25,28
aA

24,21
aA

1,576

Yield ton per hectare at water
content 14% (ton ha
-1
)
4,32
aA

5,88
aA

6,20
aA

4,33
aA

5,89
aA

6,79
aA

0,748

Biochar at 10 ton ha
-1
tend to increase the yield component of paddy rice plant as is
compared to without Biochar treatment. This is because Biochar at 10 ton ha
-1
gave the growth
media of soil microorganism. Consequently this may improve the amount of soil microorganism but
this was not followed with the increase of nutrient availibility in soil. Therefore, soil microorganism
exploit the nutrient source to energy that give in the emulation between soil microorganism with the
root plant in fulfilling nutrient. This may cause competition between soil microorganism and the root
plant.
Increase of NPK dose tend to to improve the yield component of paddy rice plant
compared to that without NPK treatment. This is caused by NPK fertilize that can directly gave the
nutrient element required by plant. So that with the existence of nutrient element provided by NPK
can fulfill the nutrient required by the plant growth. This may also repaire soil chemical properties
with sufficiency of nutrient element so that this affected the increase of yield component of paddy
rice plant.

th
Conclusions

Treatment of biochar affected significantly onthe plant height at 28 and 90 day after
planting (DAP), percentage of unfilled grain per panicle. Meanwhile, treatment of NPK affected
significantly on the plant height at 45 and 90 DAP, number of tiller 45 DAP, number of panicle per
clump, number of total grain per panicle, number of filled grain per panicle, and yield ton per ha.

References

Adiratma, E.R. 2004. Stop Rice Plant. Penebar Swadaya. Jakarta.
Gani, A. 2009. Science and Technology of Main Crop Journal. 4 (1) :33-48.
Kaderi, H. 2004. Processing Technique of Pellet Fertilizer from Weed as Compound Fertilizer and Its Effect to
Paddy. Buletin Teknik Pertanian. 9 (2).
Mori, S. and Marjenah. 1993. Mychorriza Incubation with Rice Husk Charcoal. Journal of Asosiasi Politeknik
Indonesia. Vol. I. No. 1. 2008. Samarinda.
Purnomo, J. 2009. Effect of Compound Fertilizer NPK to Yield of Ciherang Variety and Soil Chemical Properties
Inceptisol. Bogor .

th
Effects of New Foliar-Application Fertilizer Containing 5-Aminolevlinic Acid
on Yield Increase of Direct-Sowing Rice Plants

Ryuji Yoshida
a*
Keitaro Watanabe
b

a
Toyama prefectural University, Toyama, Japan
Cosmo Oil Co., Ltd., Japan

*
Corresponding author: Toyama Prefectural University, Imizu, 5180, 939-0398, Japan
Tel.: +81 766 56 7500; Fax: +81 766 56 0396
[email protected]

Abstract

In Japan, the cultivation methods for rice plants (Oryza sativa L.) in paddy field can be mainly classified into two
types, i.e. mechanical transplanting cultivation and direct-sowing. However, in the case of direct-sowing
cultivation the grain number per m
2
becomes often an excess of 30,000 grains. As the result, the decrease of
percentage of ripened grains takes places in inferior grains than in superior ones and, as a consequence, the
grain yield decreases. In the present experiment, effects of foliar application fertilizer containing 5-aminolevulinic
acid (5-ALA fertilizer: commercial name; Penta-keep) on the percentage of ripened grains in direct-sowing rice
plants were examined. This 5-ALA fertilizer was sprayed at the heading stage of cvs. Koshihikari and
Tenkomori, the promotive effect on the yield increase of grains was found in both the cultivars tested. It should
be noted that the high yielding effects were at least in part supported by the increasing of grain filling in inferior
grains and superior, especially in inferior grains. On the other hand, the excellent effect of 5-ALA fertilizer was
found in the aerial spray by small automated helicopter. From all results, we emphasize that the application of
foliar application fertilizer containing 5-ALA are very useful to achievehigh yield of direct-sowing rice plants.

Keywords: 5-aminolevulinic acid (5-ALA), direct-sowing of rice plants, new foliar-application fertilizer (-ALA
fertilizer; Penta-keep), yield-increase

Introduction

In Japan, the cultivation methods for rice plants (Oryza sativa L.) in paddy field can be
mainly classified into two types, i.e. mechanical transplanting cultivation and direct-sowing. In recent
year, the growing area using the latter cultivation type progressively tends to the extension because
of the establishment of labor-saving cultivation for rice. However, the grain number per m
2
of rice
plants cultivated by direct-sowing becomes often an excess of 30,000 grains. As the result, the
decrease of percentage of ripened grains take places in inferior grains than in superior ones and, as
a consequence, the grain yield decreases.
Yoshida et al. (1996) reviewed that 5-aminolevulinic acid (5-ALA) has often promoting
effects on yield increase of crops. Hotta et al. (1997) reported that ALA has plant growth regutating
properties at low concentration (<30ppm) and the foliar application of this compound enhanced the
growth and yield of kidney beans, barley, potato and garlic. However, there is insufficient
information about the promotive effect of ALA on the grain filling of rice plants. The supply of large
amount for 5-ALA having high-quality and inexpensive price has already been successfully
achieved by Tanaka (1995). A new foliar-application fertilizer containing 5-aminolevlic acid using the
extension in agriculture field was also developed by Cosmo Oil Research Group (Tanaka et al.
2006). Commercial name for this fertilizer is PENTAKEEP super or 5-ALA fertilizer.
This experiment, therefore, was carried out to clarify whether the foliar application of 5-ALA
fertilizer was able to alter the percentage of ripened grains, especially in direct-sowing rice plants.
The utility for achieving high yielding grains of direct-sowing rice cultivation was discussed.

th

Experiment I (2009)
Rice cultivation. Rice cultivars used were Koshihikari (medium maturing variety) and
Tenkomori (late maturing variety) in Toyama, Japan. The coating pregerminated seeds with calcium
peroxide (CaO
2
of 2-fold) were sown in paddy soil by using direct-shooting seeder. The sowing rate
of both the cultivars was 2.52.8 kg per 0.1ha.The controlled availability fertilizer (LPs,
N:P:K=18:12:12 ) was basally dressed at rate of 3035kg per 0.1ha. When the growth of rice
plants reached the full heading time, 5-ALA fertilizer was sprayed to the whole plant.
Spray of 5-ALA fertilizer. Fertilizer 5-ALA was composed of N at 8.0%, P
2
O
5
at 5.0%, K
2
O
at 3.0%, MgO at 3.0%, Fe at 0.29%, Mn at 0.12% and other micro-elements, but the concentration
of 5-ALA was not only open. At the full heading time, 5-ALA fertilizer was sprayed weekly twice to
whole plants. The concentration and application volume of 5-ALA fertilizer were 2000-fold solution
and 200 liter per 0.1ha, respectively. The percentage of ripened grains, such as superior and
inferior gains of panicle, was determined at the harvesting time. Yield component of rice plants and
quality of grains was also observed.

Experiment II (2010)
Cv. Koshihikari was grown in paddy field. The rates of basal-dressing fertilizer were the
same as those used in Experiment I. The application of 5-ALA fertilizer was sprayed by small
automated helicopter. In this case of aerial application, the concentration and application volume of
5-ALA fertilizer were 8-fold solution and 0.8 liter per 0.1ha, respectively. The effects of spraying 5-
ALA fertilizer on the percentage of ripened grains and yield component were evaluated at the
harvesting stage.


In Japan, the yield decrease of direct-sowing rice plants is attributed to the excess of grain
number per m
2
(more than 30,000 grains). This excess of unfulled grains per m
2
takes place the
increase of sterile and imperfect grains in panicle. In practical producing field of direct sowing
cultivation, the percentage of ripened grains in cv. Koshihikari was well known to vary the range of
6574%. For achieving high-yielding grains in direct-sowing rice cultivation, therefore,
understanding the effects of 5-ALA fertilizer was particularly important. In this experiment, the
unfulled grains of panicle were divided into superior and inferior grains (Figure.1).

Superior grain
Inferior grain
Uppermost internode
Fig.1 Clssification of superior and inferior
grains in panicle.

Figure 1. Classification of superior and inferior grains in panicle.

th
All grains attached directly to primary branches and the terminal grains of secondary
branches were defined as superior grains and the grains on secondary branches, excepting the
terminal one, were defined as inferior grains. The following data (Tables 1, 2, 3) were obtained from
Experiment I. Table 1 shows the effects of spraying 5-ALA fertilizer on yield component. In the case
of cv. Koshihikari, the rate of grain-straw was 1.1 in both the control plants (untreated-treated with
5-ALA fertilizer) and the plants treated with 5-ALA fertilizer. The unfulled grain number per m
2
was
about 33,000 in both the plants. In the case of cv.Tenkomori, the grain-straw ratio and unfulled
grain number were 0.9 and 30,00033,000, respectively. The yield components in both the
cultivars did not vary with the spraying 5-ALA fertilizer.

Table 1. Effects of 5-ALA fertilizer on yield component

Cultivar Treatment
5-ALA
fertilizer
Unfulled
grain
weight
(g/hill)
Straw
weight
(g/hill)
Unhulled
grain -
straw ratio
Panical
number
per hill
Unhulled
grain
number
per hill
Unhulled
grain
number
per m
2

Koshihikari Untreated
(control)
51 48 1.1 22.9 1.839 33.470
Treated 52 49 1.1 23.0 1.806 32.860
Tenkomori Untreated
(control)
45 48 0.9 21.2 1.654 30.103
Treated 46 51 0.9 21.7 1.786 32.504
1. The density of direct-sowing rice plants is 21~24 per m
2

2. The value show the means of 3 replications. The number of hills tested is 240.

The percentage of ripened grain in rice plant treated with 5-ALA fertilizer is shown in
Tables 2. As was expected, the 5-ALA fertilizer enhanced the percentage of ripened grains. This
increase was much more marked in the inferior grains than in the superior ones. The extent of the
increase in both the cultivars brought about by the spraying treatment amounted from 13.6 to 29.9%
(cf. control) in the inferior grains. Thus, the spraying treatment of 5-ALAfertilizer significantly
affected the grain filling of inferior grains (p0.05).

Table 2. Effect of 5-ALA fertilizer on percentage of ripened gains

Cultivar
Treatment 5-
ALA fertilizer
Unhulled
grain number
per panicle
Ratio of grains per panicle
(%)
Percentage of ripened grain
(%)
Superior
grains
Inferior grain
Superior
grains
Inferior grain
(control)
80.3+45 77.9+0.7 22.1+0.7 82.7+3.0
a
54.9+2.1
b

Treated 78.5+5.5 82.8+2.3 17.2+2.3 88.8+2.8
a
84.8+4.6
a

Tenkomori Untreated
(control)
78.0+7.0 71.8+2.6 28.2+2.6 94.0+3.3
a
79.8+4.4
b

Treated 82.3+2.8 72.7+3.0 27.4+3.0 95.7+1.4
a
93.4+1.5
a

1.Date are means+SE of 150 panicles.
2.Different letters within columus in each cultivar indicate significant differences by Tukeys multiple range test (p<0.05)

As for the 1,000 grain weight, the cv. Tenkomori showed higher value in inferior grains
than that in superior ones (Table 3). In the case of cv. Koshihikari, the fulled grain yield of the plants
treated with 5-ALA fertilizer was 627.5kg per 0.1ha, this value was higher than that of control plants
(Table 4). The effect of spraying 5-ALA fertilizer also was much more marked in the case of cv.
Tenkomori. The degree of yield increased was 145.5kg per 0.1ha. These findings showed that 5-
ALA fertilizer acts as a regulator for yield increase of rice plants through a steady increase of grain
filling, especially in inferior grains. Regarding the physiological function of 5-ALA, Tanaka (1995)
th
has been reported in radish plants that 5-ALA enhanced the activity of photosynthesis and
suppressed the rate of respiratory activity. Yoshida (1996) showed that the accumulation fractan in
rakkayo and shallot plants was increased by 5-ALA application. From the results obtained here and
these findings, the steady increase of the percentage of ripened grains by the application of 5-ALA
fertilizer seemed to be dependent on the activity of photosynthesis during the grain filling period.
However, the physiological functions of this fertilizer during maturation of rice grains are still almost
unknown at the present.

Table 3. Effect of 5-ALA fertilizer on yield and quality of gains (hulled grains)

Cultivar
Treatment 5-
ALA fertilizer
1000 grain
weight (g)
Grain yield
(kg/0.1ha)
Quality of grain (%)
Protein
content (%)
Amilose
content (%)
Index of
paratability
(control)
22.2.0+0.5 506.6 6.1 18.7 73
Treated 22.0+0.5 627.5 5.9 18.7 74
Tenkomori Untreated
(control)
22.3+0.3 583.3 6.0 18.9 74
Treated 23.7+0.5 728.8 6.0 19.0 75
1.means+SE
2.quality of grains is determined by Satake rice*grain paratability tester

Table 4. Effects of 5-ALA fertilizer sprayed by the helicopter on the percentage of ripened grains in cv.
Koshihikari

Treatment 5-ALA
fertilizer
1000 grains weight
(g)
Percentage of ripened grains (%) Grain yield
(kg/0.1ha) Superior grains inferior grams
Untreated (control) 21.2+0.3
a
83.5+3.9
a
68.7+5.1
b
670.0
Treated 20.8+0.2
a
86.2+5.0
a
79.2+4.3
a
696.2
1.Data are means+SE of 150 panicles
2. Different letters within columns indicate significant differences by Tukeys multiple range test (p=0.05)

References

Hotta Y., T. Tanaka, H. Takaoka, Y. Takeuchi and M. Konnai. 1997. Promotive effects of 5-aminolevulinic acid
on the yield of several crops. Plant Growth Regulation. 22:109-114.
Tanaka T.1995.Application and production of 5-aminolevlinic acid by photosynthetic fungi, Rhodobacter
sphaeroides. Doctor thesis (Hroshima University) . 5-138.
Yoshida R., Y. Hotta, T. Tanaka, Y. Takeuchi and M. Konnai, 1996. Agricultural use of 5-aminolevulinic acid 2
nd

International Crop Science Congress. Abstracts 392. New Delhi.
Yoshida R., T. Tanaka and Y. Hotta. 1996. Regulation of fractan accumulation in rakkyo (Allium Bakeri) and
shallot (A. ascalonicum) by 5-aminolevulinic acid. Proceedings of Plant Growth Regulator Society of
America. 177-182.

th
Yield Stability Evaluation of Upland Rice Lines Obtained
from Anther Culture

Deni D Sulaeman
a
, Bambang S Purwoko
b*
, Iswari S Dewi
c
, Muhamad Syukur
b
, Desta
Wirnas
b
, Heni Safitri
d

a
Graduate Student of Plant Breeding and Biotechnology Major, the Graduate School of Bogor Agricultural
University,
b
Department of Agronomy and Horticulture, Faculty of Agriculture, Bogor Agricultural Universit,
c
Indonesian Center for Agricultural Biotechnology and Genetic Resources Research and Development, Bogor,
d
Indonesian Center for Rice Research, Bogor
*Corresponding author: Jln Meranti, Darmaga, Bogor 16680 Indonesia.
Tel: +62 251 8629353.
E-mail address: [email protected]

Abstract

The objective of this research was to study the adaptation and yield stability of upland rice lines obtained from
anther culture. Ten upland rice doubled-haploid (DH) lines were tested for their potential yield in eight different
locations (in Provinces of Lampung, West Java, Central Java, Yogyakarta, East Java - Indonesia) in the rainy
season of 2010/2011 along with two check varieties (Way Rarem and Batutegi). In each location, the design was
Randomized Complete Block Design with four replicates. The method of Francis & Kannenberg, Finlay &
Wilkinson, Eberhart & RusseIl and AMMI (Additive Main Effect Multiplicative Interaction) were used to analyze
the adaptation and yield stability of the tested DH lines. The results indicated that the line showing the most
stable yield in different environment was I5-10-1-1 followed by WI-44, and IG-38. I5-10-1-1 produced 4.01 tons
of dry grain per hectare. The line showing the highest yield was WI-44, and this line produced 4.72 tons of dry
grain per hectare. Visualization with AMMI showed that IW-56 and IW-67 lines were specifically adapted in
Purworejo, O18-b-1 is specifically adapted in Bogor, and IG-19 is specifically adapted in Malang, respectively.

Keywords: upland rice, DH lines, yield stability

Introduction

Efforts to increase the food production, especially rice, through the utilization of dry land
can be reached by breeding upland rice, since the high-yielding upland rice varieties may be
accepted by farmers. Anther culture has been reported to produce doubled-haploid (DH) plants or
pure lines in a short time (Dewi et al., 1996). On the contrary, conventional breeding will require a
long period of time (more than 5 years) in obtaining pure lines as a result of combining the desirable
traits of different varieties or parents. Through anther culture of F1, several number of upland rice
DH lines were obtained from previous experiment, i.e. IW-56, IW-67, IG-19, IG-38, and GI-8 lines
tolerant to low light intensity or shade (Sasmita et al., 2006); III3-4-6-1 and I5-10-1-1 lines tolerant
to aluminum toxicity (Herathwati et al., 2009); while O18-b-1 and B13-2e lines tolerant to both
shade and Al toxicity (Purwoko, 2007). Those DH lines need to be evaluated further.
Subandi (1981) asserted that in the establishment of superior varieties breeders need to
pay attention to the yield stability in a systematic and continuous manner, starting from the
formation of the basic population to test varieties. Adaptability evaluation in different growing
environments need to be done because of the diversity of land, soil, cultivation, cropping patterns
and planting season in Indonesia. The diversity of the growing environment will affect the yield per
unit area, because the plant growth is a function of genotype and environment (Allard, 1960).
Appearance of plants depends on the genotype and environmental conditions where the plant grew,
as well as the interaction between the two. Yield stability evaluation through a series of multi
location test is an important stage before the varieties can be released. Therefore, this research
th
was aimed to study the adaptation and yield stability of upland rice DH lines obtained from anther
culture in 8 different environments.


The yield stability test of upland rice was held at eight locations in the rainy season during
October 2010 until April 2011. Testing locations spread across Java and Sumatra, namely: the
Taman Bogo - Lampung, Natar - Lampung, Cikarawang Bogor - West Java, Sukabumi - West Java,
Indramayu - West Java, Purworejo - Central Java, Wonosari - Gunung Kidul, and Malang - East
Java. A total of 12 genotypes were used as test material, which consisted of 10 upland rice DH lines
obtained from anther culture, i.e. III3-4-6-1, I5-10-1-1, WI-44, GI-7, O18-b-1, IW-67, IG-19, IG-38,
IW 56, and B13-2e, while Batutegi and Way Rarem.were two check varieties used for comparison.
The experimental design was Randomized Complete Block Design with four replicates. An
experimental unit consisted of 4 x 5 m
2
plot. Each of the tested genotypes were planted with a
spacing of 30 x 15 cm. Observations and data analysis were conducted on dry grain yield per
hectare. The method of Francis & Kannenberg, Finlay & Wilkinson, Eberhart & RusseIl and AMMI
(Additive Main Effect Multiplicative Interaction) were used to analyze the adaptation and yield
stability of the tested DH lines.


The variance analysis of pooled data at eight test locations showed the occurrence of
interaction between lines (genotype) and environment (G E) (Table 1). The existence of such
interactions will cause each lines responded differently to the environment in which testing was
conducted. The response was mainly shown by the fluctuations in grain yield. A genotypes or
varieties though, will not always produce the same great results if planted in different environments.
This is caused by the large diversity of the macro geophysical environment that will provide the
large environmental diversity for plant growth as well (Satoto et al, 2009).

Table 1. Analysis of variance of pooled data at 8 locations

Source of Variation df SS MS F value
Location 7 123.18 17.60 30.68 **
Rep/Location 24 66.29 2.76 4.82 **
Lines 11 123.48 11.23 19.57 **
Lines Location 77 230.93 3.00 5.23 **
Error 264 151.41 0.57
Total 383 695.30
Notes : ** very significantly different

The average of dry grain yield of WI-44 is able to outperform other lines and check
varieties at two locations, namely Bogor and Malang (Table 2). The average dry grain yield showed
that only the WI-44 and IW-67 was able to outperform Batutegi varieties, while Way Rarem varieties
only surpassed by WI-44. The difference in average yields between WI-44 with Batutegi was 0.34
tons/ha, where WI-44 was about 7.67% higher than Batutegi. The difference in average yield
between IW-56 with Batutegi was 0.01 tons/ha or approximately IW-56 was only 0.2% higher than
th
Batutegi. However, the difference in average yields between WI-44 with Way Rarem was 0.1
tons/ha or WI-44 approximately 17.2% higher than Way Rarem.

Tabel 2. The average dry grain yield (tons/ha) of upland rice DH lines in every test location

DH Lines
LOCATION Yield
Average
(tons/ha)
Indra-
mayu
Wono-
sari
Purwo-
rejo
Suka-
bumi
Bogor Malang
Lam-
pung
Taman
Bogo
III3-4-6-1 2.95 2.39 4.88 2.59 1.52 3.11 2.79 3.36 2.95
I5-10-1-1 2.88 3.44 4.62 4.70 4.81 4.11 2.99 4.51 4.01
WI-44 3.24 3.74 5.55 5.69 5.40 5.98 4.15 4.02 4.72
GI-7 2.72 2.60 2.53 3.73 5.16 5.10 2.68 3.69 3.52
O18-b-1 2.17 2.41 3.19 3.45 5.04 3.58 2.68 2.52 3.13
IW-67 3.14 4.35 6.94 5.08 4.14 3.90 3.76 3.85 4.39
IG-19 1.86 3.61 2.66 3.40 3.79 4.32 2.26 4.48 3.30
IG-38 2.06 3.38 3.28 3.70 2.89 4.51 2.31 4.13 3.28
IW-56 2.51 4.39 6.81 4.14 2.69 3.25 3.53 3.21 3.82
B13-2e 2.91 2.52 3.54 4.07 4.22 4.66 4.00 4.41 3.79
Batutegi 3.01 3.14 5.89 4.16 3.04 5.63 4.66 5.54 4.38
Way Rarem 3.79 3.87 4.35 6.95 3.46 5.33 4.99 4.24 4.62
Average 2.77 3.32 4.52 4.30 3.85 4.46 3.40 4.00 3.81
CV (%) 24.0 23.2 20.6 15.6 23.1 10.6 12.6 25.7

The parameters of stability of dry grain yield of upland rice DH lines from eight locations
are presented in Table 3. Lin et al.(1986) suggested three concepts of stability. A genotype is
considered to be stable if: (1) the variance among environment is small, (2) the response to its
environment is parallel to the mean response of all genotypes in the trial, (3) residual mean square
(MS) from the regression model on the environmental index is small.

Tabel 3. Parameters of stability of dry grain yield of upland rice DH lines from eight locations

DH lines Yield (t/ha) SD
i
CV
i
b
i

2
R
i
2

III3-4-6-1 2.95 1.09 32.51 0.64 * 1.04 0.31
I5-10-1-1 4.01 0.74 19.74 1.10 ns 0.73 0.64
WI-44 4.72 1.02 22.17 1.52 * 1.25 0.43
GI-7 3.53 1.21 31.16 0.77 * 1.40 0.29
O18-b-1 3.13 1.01 29.55 0.76 * 0.98 0.37
IW-67 4.39 1.00 26.56 1.31 * 1.58 0.32
IG-19 3.30 1.23 28.85 0.84 ns 1.05 0.37
IG-38 3.28 1.10 25.70 1.02 ns 0.82 0.47
IW-56 3.82 1.38 35.92 1.18 ns 2.19 0.20
B13-2e 3.79 1.04 19.71 0.78 * 0.65 0.67
Batutegi 4.22 1.20 27.98 1.17 ns 1.75 0.29
Way Rarem 4.62 1.15 24.42 0.90 ns 1.47 0.35
Rata-rata 3.81 1.00
Notes : SDi= Standard deviation of genotype; CVi=Coeficient of variance of genotype;, bi= Coefficient of regression of
genotype, value of b
i
* (significantly different with 1), ns (not significantly different with 1);
2
=parameter of deviation;,
R
i
2
=Coefficient of determination.
th
Francis & Kanennberg (1978)
Francis and Kanennberg (1978) measure the stability by using the coefficient of variability
(% CV
I
) of each genotype tested in multiple environments. The small values of its coefficient of
genotype diversity meant that the genotype is more stable. Moedjiono and Mejaya (1994)
categorized the value of the coefficient of genotype diversity in four groups, namely low (<25%),
rather low (25 -50%), rather high (50-75%), and high (75-100%). Therefore, based on those criteria
the DH lines tested in this study fell into of low and rather low groups. I5-10-1-1, WI-44, B13-2e, and
Way Rarem have a low coefficient of genotype diversity, thus classified as stable.

Finlay and Wilkinson (1963)
Stability analysis of Finlay and Wilkinson (1963) is a method of measurement stability that
is based on the regression coefficient (b
i
) between the average yields of a genotype with a general
average of all genotypes tested in all test environments. This analysis can explain the phenomenon
of stability and adaptability of a genotype. Finlay and Wilkinson categorize standard b
i
values of
stability in the three groups, namely (1) the stability is below the average, if the value of b
i
> 1, (2)
stability is equivalent the average, if the value of
bi
= 1, (3) stability is above the average, if the value
of b
i
<1.
Based on those criteria, Batutegi and Way Rarem and also three DH lines had b
i
values
not significantly different from 1, i.e. I5-10-1-1, IG-19, IG-38, and IW-56. Those DH lines were
categorized as a stable line, which meant the lines will be able to adapt to the large environment.
Lines with the stability below the average were WI-44 and IW-67 with the b
i
of 1.52 and 1.31, while
the lines with the stability above the average were III3-4-6-1, GI-7, O18-b-1, and B13-2e with b
i

values of 0.64, 0.77, 0.76, and 0.78, respectively. Lines that have below-average stability are
sensitive to environmental changes and adapt to particular environmental benefit (favorable). The
lines which have above average stability are generally able to adapt to marginal environments.

Eberhard dan Russel (1966)
Stability analysis of Eberhard and Russell (1966) is a measure of stability based on the
deviation from the regression of the average value of genotype on the environmental index. A
genotype is stable if residual mean square (MS) from the regression model on the environmental
index is small. Parameter stability seen from the deviation value (
2
) and coefficient of determination
(R
i
2
) of the tested genotypes. Model stability of a genotype is good if it has little
2
value and large
R
i
2
value (approaching 1).
Based on these parameters, two DH lines namely B13-2e and I5-10-1-1 had the smallest
value of
2
, i.e. 0.65 and 0.73 (Table 3). Coefficient of determination (R
i
2
) from these two lines also
had the largest value among lines and other varieties, i.e. 0.67 and 0.64. Therefore, the regression
model used to estimate the stability of those two lines are better than the other lines.

AMMI (Additive Main Effect Multiplicative Interaction)
Due to limited visualization of graphs that are only capable of displaying two-dimensional
graph, then the model described in this paper is AMMI2. AMMI2 model can explain the diversity of
the interaction effect up to 70.98%. Bi-plot of interaction affects AMMI2 model for the dry grain yield
of upland rice DH lines are presented in Figure 1. The bi-plot of principal components 1 and 2 can
explain the main components of lines which are stable at all location test or specific to a particular
location. Mattjik and Sumertajaya (2000) states that a line or genotype is said to be stable when
close to the axis or point (0,0). The lines or genotypes that are far away from the axis but close to
the line location, then the lines were classified as specific location lines. Based on these, lines that
are stable at all location test are I5-10-1-1, WI-44, IG-38, and Way Rarem. IW-56 and IW-67 were
specific to the location of Purworejo, O18b-1 line-specific for the location of Bogor. IG-19 is specific
to the location of Malang.

th

Figure 1. Bi-plot of interaction effects AMMI2 model for the dry grain yield of upland rice DH lines derived from
anther culture

Conclusions
The DH line showing the most stable yield in different environment was I5-10-1-1 followed
by WI-44, and IG-38. Visualization with AMMI showed that IW-56 and IW-67 lines were specifically
adapted in Purworejo, O18-b-1 was specifically adapted in Bogor, and IG-19 was specifically
adapted in Malang.

References

Allard RW. 1960. Principles of Plant Breeding. J Wiley and Sons. New York. 485 p.
Dewi IS, Hanarida I, Rianawati S. 1996. Anther culture and its application for rice improvement program in
Indonesia. Indon. Agric. Res. Dev. J. (18) : 51-56.
Eberhart SA, Russel WA. 1966. Stability parameters for comparing varieties. Crop Sci. 6:36-40.
Finlay KW, Wilkinson GN. 1963. The analysis of adaptation in a plant-breeding programme. Aust. J. Agric. Res
14:742-754.
Francis TR, Kannenberg LW. 1978. Yield stability studies in short-season maize. A descript method for grouping
genotypes. Can. J. Plant Sci. 58:1029-1034.
Herawati R, Purwoko BS, Dewi IS. 2009. Keragaman genetik dan karakter agronomi galur haploid ganda padi
gogo dengan sifat-sifat tipe baru hasil kultur antera. J.Agron. Indonesia 37(2) : 87-94.
Lin CS, Binns MR, Levkovitch LP. 1986. Stability analisis : Where do we stand?. Crop Science. Vol. 26 : 894-
900.
Mudjiono, Mejaya MJ. 1994. Variabilitas genetik beberapa karakter plasma nutfah jagung koleksi Balittas
Malang. Zuriat 5(2) : 27-32.
Purwoko BS. 2007. Aplikasi kultur antera dan marka RAPD dalam perakitan padi gogo toleran cekaman
lingkungan. Laporan Riset Unggulan Terpadu Bidang Pertanian dan Pangan.
Sasmita P, Purwoko BS, Sujiprihati S, Hanarida I, Dewi IS, Chozin MA. 2006. Evaluasi pertumbuhan dan
produksi padi gogo haploid ganda toleran naungan dalam sistem tumpang sari. Bul. Agron. (34) (2) 79-
86.
Satoto, Utomo STW, Widyastuti Y, Rumanti IA. 2009. Usulan Pelepasan Varietas Padi Hibrida H45, H47, H64,
H68 dan H78. Makalah pada Sidang Pelepasan Varietas, Desember 2009.
Subandi, 1981. Genotype x environment interactions in corn variety test. Food Crop 65:1-9.

th
Yield and Blast Resistance Evaluation of Upland Rice Lines
with New Plant Type Characters

Jose MA Ornai
a
, Bambang S Purwoko
b*
, Desta Wirnas
b
, Iswari S Dewi
c
, Heni Safitri
d

a
Graduate Student, Plant Breeding and Biotechnology Major, the Graduate School,
b
c
Indonesian Center for Agricultural Biotechnology and Genetic Resources Research and Development, Bogor
d
Indonesian Center for Rice Research, Bogor
* Corresponding author: Jln. Meranti, Darmaga, Bogor 16680 Indonesia.
Tel/ Fax: +62 251 8629353.
[email protected]

Abstract

The present studies were conducted to determine agronomic characters, genetic variability, broad sense
heritability (h
2
bs
)

and blast resistance of doubled haploid rice lines and to obtain new plant type (NPT) of upland
rice with high yield potential and blast resistant. The research was conducted in Bogor and Sukabumi, Indonesia
started from November 2010 to June 2011. There were 14 genotypes evaluated namely the new lines of rice
from anther culture (FG1-66-2-1, FG1R-108-1-1, FG1R-51-2-1, FM1-14-1-1, FM1-14-1-2, FM1-25-1-1, FM1-25-
1-2, FM1-57-1-2, FM1R-32-1-1, FM1R-23-1-1, FG2-47-1-3, FM1R-19-2-4, FM2-12-1-1, FAT-4-1-2), as well as
Fatmawati, Limboto and Batutegi as check varieties. The experimental design used was randomized block
design (RBD). The results showed that there was variability on agronomic traits and blast resistance among
lines evaluated. FG2-47-1-3 did not have complete characters of NPT, but the line had superior characteristics
such as high percentage of filled grain, medium days to harvest, medium height, medium 1000-filled grain
weight, stay green when harvested and high resistance to blast disease. The results also indicated that the
tested population had high heritability (h
2
bs
) in leaf blast and neck blast resistance, plant height, filled grain per
panicle, days to harvest, number of grain per panicle and 1000-filled grain weight. They showed high variance
coefficient for leaf blast and neck blast resistance, flag leaf length and percentage of filled grain.

Keywords: new plant type, upland rice, blast resistance, heritability.

Introduction

Rice is staple food in Indonesia. Population growth will increase national rice consumption
(Prasetyo 2008). In the year of 2000-2006, population growth rate was 1.36% with per capita
consumption of rice at 137 kg. It is estimated that in 2010, 2015 and 2020 consumption of rice and
a population with declining population growth rate assumption of 0.03%, respectively was 32.13
million tons with a population of 235 million, 34.12 million tons with a population of 249 and 35.97
million tons with population of 263 million inhabitants (Puslitbangtan 2007).
Increase in national rice production must be continually pursued. One of the effort to
increase national rice production is the use of dry land to grow upland rice so as to support national
food security (Puslitbangtan 2007). Indonesia has 11.6 million ha of dry land (BPS 2005). Dry land
used for planting upland rice in 2010 reached 1.13 million ha (Deptan 2011), so there are still
opportunities to expand the area of upland rice cropping. Upland rice production reached 3.45
million tons with yield of 3.05 tons/ha (Deptan 2011). Contribution of upland rice to the national rice
production is still low at 5% (Prasetyo 2008).
Increased productivity of upland rice can be done by developing a new plant type (NPT) of
upland rice lines. NPT ideotype characters desired, among others, are plant height <150 cm,
number of productive tillers > 6, number of grain per panicle > 150, short growth period (105-124
days), good filled grain (> 75%), 1000-filled grain weight more than 28 g (Herawati 2010).
th
Based on previous research, rice lines were obtained from crosses of a new plat type of
lowland rice Famawati with local upland rice varieties from the island of Buru namely Fulan Telo
Gawa (FTG) and Fulan Telo Mihat (FTM) through anther culture (Safitri 2010). Lines need to be
further evaluated both morphological and agronomic characters/ performance and resistance to
blast disease.
Blast disease is caused by fungus Pyricularia grisea. The disease can reduce the
productivity of upland rice between 11-50% (Beker at al. 1997; Scardaci et al. 1997). Fungus
Pyricularia grisea infects leaves at vegetative stage, called leaf blast, while in the generative stage,
the pathogen also infects the panicle neck, called neck blast (BB Biogen 2009).
The present studies were conducted to obtain information on performance of agronomic
characters and resistance to leaf blast and neck blast in the new rice lines. In addition, this study
was also aimed to select a new plant type of upland rice lines with high yield and resistant to blast
disease.


The research was conducted in Babakan Experiment Station, University Farm, Bogor
Agricultural University and in the village of Bojong, Cikembar Sub-District, Sukabumi District, West
Jawa, Indonesia (endemic blast region) from November 2010 to April 2011. The genetic materials
were 15 doubled haploid upland rice lines obtained from anther culture of F1, crosses between
Fatmawati and Fulan Telo Mihat or Fulan Telo Gawa (Safitri 2010). Fatmawati, Batutegi and
Limboto were used as a check varieties.
This study used a randomized blocked design with lines as treatment and consisted of 3
replicates. Experimental unit in Bogor was done in the form of a plot of 3 x 3.6 m. Three seeds
were planted per hill with spacing of 30 x 20 cm. In Sukabumi, each replicate was 10 x 2 m. One
seed was planted per hill with spacing of 20 x 10 cm. Fertilizer use were 10 tons of manure/ha, 200
kg of Urea/ ha (given: 20% age 1 week, 40% at age 4 weeks and 7 weeks), 100 kg/ha of KCl and
100 kg/ha of SP36. Maintenance was performed in accordance with the conditions and crop needs
in the field.
Observations were made on 5 plants per plot on variables: plant height, number of
productive tillers, days to harvest, total grain per panicle, percentage of filled grain, 1000-filled grain
weight, productivity, the scale and intensity of leaf blast and neck blast disease. The data obtained
were analyzed by F test, if significantly different then followed by Dunnett test on a level of
significance 5%, range estimation and analysis component of the correlation between characters.
The intensity of leaf blast disease was calculated with the formula: I = (n x v) / (N x V)
x100%, where I = intensity of disease, n = number of plants infected, v = scale of plant infected, N =
total number of plant observed, V = the highest scale of blast disease (9) (IRRI 1996). Resistance to
blast disease were classified into resistant, if I 10% and susceptible, if I> 10%. Observation of the
panicle neck blast was performed at harvest which includes the scale and intensity of the disease.
The intensity was calculated by: I = n / N x 100%, where I = intensity of blast disease, n = number
of panicles infected, N = number of panicles observed. The scale of the disease was determined
based on the evaluation system on panicle neck blast disease from IRRI (1996) as follows: 0 = no
symptom, 1 = infection of less than 5%, 3 = 5-10% infected, 5 = 11-25% infected, 7 = 26-50%
infected, 9 = more than 50% infected. Panicle neck blast resistance were classified into resistant
(score 0-1), moderately resistant (score 3-4), moderately susceptible (score 5-6) and susceptible
(score 7-9).

th

The variance analysis showed that the genotype effect was significant on all characters
observed. This indicated that there were differences between doubled haploid lines of upland rice.
The coefficient of variability (CV) ranged between 2.5 and 43.6% (Table 1). Plant height ranged
from 73.8 to 124.0 cm (Table 1). Higher plant meets the criteria as a new plant type of upland rice
lines. According to Herawati (2010) and Abdullah et al. (2005), height of new plant type of upland
rice is under 150 cm and for a new plant type of lowland rice is 80-100 cm. The height of some lines
tested (FG1R-108-1-1, FG1R-51-2-1, FM1-14-1-1, FM1-57-1-2-32-FM1R 1-1 FG2-47-1-3) were
significantly different from and were higher than Fatmawati (Table 1). Nonetheless, plant height still
meets the general criteria for the plant height of new types of upland rice lines.
The number of productive tillers of 14 lines tested ranged from 6.5-15.5. According to Peng
et al. (2008), the number of productive tillers are ideal for a new pant type of rice (NPT) is 10-15 for
lowland rice, while according to Herawati (2010) the number of productive tillers for a new plant type
of upland rice lines is > 6. Fatmawati has the potential to produce 6-14 tillers. The number of tillers
Fatmawati in upland conditions conducted in this study was 13.

Table 1. Agronomic performance of doubled haploid upland rice lines

Lines PH NPT DH TS FG PFG B1000 YP
FG1-66-2-1 91.2 11.8 127.7 177.6 59.4 33.3 29.7
e+
0.52
FG1R-108-1-1 124.0
a+
6.5
a-
130.3 137.4
e-
11.6
e-
17.1 26.3 0.24
e-

FG1R-51-2-1 116.6
a+
7.9 130.0 154.0 7.5
e-
4.5
e-
29.3
e+
0.08
e-

FM1-14-1-1 102.7
a+
8.3 126.7 114.7
e-
18.4
e-
15.0 30.3
e+
0.41
FM1-14-1-2 97.6 10.4 128.3 100.5
e-
13.0
e-
11.7
e-
29.3
e+
0.26
e-

FM1-25-1-1 90.4 8.4 134.3
a+
122.3
e-
5.4
e-
3.9
e-
29.0
e+
0.12
e-

FM1-25-1-2 93.2 8.1 134.7
a+
115.1
e-
15.0
e-
2.1 25.3 0.65
FM1-57-1-2 112.1
a+
11.3 134.3
a+
133.6
e-
29.5
e-
8.3
e-
31.0
e+
1.48
FM1R-32-1-1 118.7
a+
10.7 130.0 128.7
e-
46.4 37.1 33.3
e+
1.06
FM1R-23-1-1 77.4 11.3 131.3
a+
115.8
e-
2.1
e-
2.3
e-
25.3 0.08
e-

FG2-47-1-3 110.3
a+
15.5 128.0 118.4
e-
80.1 68.3 25.3 2.00
FM1R-19-2-4 73.8 13.3 128.3 69.0
e-
2.5
e-
32.8
e-
25.7 0.04
e-

FM2-12-1-1 94.0 11.2 122.0 61.3
e-
22.3
e-
34.8 23.3
e+
0.31
FAT-4-1-2 79.1 11.1 128.3 112.7
e-
40.0 34.8 28.3 0.72
Fatmawati(a) 84.6 13.0 123.3 102.6 11.5 10.0 25.7 0.31
Batutegi (e) 118.6 10.7 126.0 213.3 114.2 53.8 26.3 1.88
CV (%) 6.6 12.5 2.5 9.9 43.6 40.0 3.4 26.3
Note: Numbers followed by the letters a+ and a- column differ significantly higher and differ or lower with Fatmawati. Numbers
and e+ e- is significantly different higher or lower than Batutegi based on the Dunnett test at significant level of 5%. PH =
plant height, NPT = Number of productive tillers, DH = days to harvest. TS = Total spikelet, FG = number of filled grain,
PFG = Percentage of filled grain, B1000 = 1000-filled grain weight, YP = Yield potential (tons/ha), CV = coefficient of
variability.

According to Herawati (2010), the days to harvest of new plant type of upland rice ranged
from 105 to 124 days. Days to harvest of the lines tested ranged between 122-134.3 days. The line
that meet the criteria was FM2-12-1-1. Fatmawati variety showed 123.3 days to harvest. Some of
the lines tested (FM2-25-1-1, FM1-25-1-2, FM1-57-1-2, FM1R-23-1-1) had significantly different
days to harvest and were longer than that of Fatmawati.
Batutegi was a variety with the highest number of spikelet per panicle (213.3 spikelets), but
only had percentage of filled grain of 53.8 percent. The number of spikelet per panicle of the lines
tested ranged between 61.3-177. Lines with the highest total number of spikelets was FG1-66-2-1
(177), but only 59.4 filled grain per panicle, that was 33.3%. Despite of only having a total number of
spikelet 118.4, FG2-47-1-3 has the highest percentage of filled grain. According to Herawati (2010)
the number of spikelet per panicle of NPT upland rice is more than 150 per panicle. Based on the
number of spikelet per panicle, only FM2-12-1-1 and FG1R-51-2-1 meets the criteria. However,
they had low percentage of filled grain. Weight of 1000 grain of rice ranged from 23.3 to 33.3 g
th
(Table 1). Variety has comparable weight of 1000 grain, ranging from 25.7 and 26.3 g. Of the 15
lines tested, 8 lines have weight of 1000 grain had more than 28 g (Herawati 2010) (Table 1).
Yield of 14 lines tested ranged from 0.04 to 2.00 tons/ha. Yield of varieties were 0.31 and
1.88 tons/ha. Batutegi had the highest yield among the check varieties (1.88 tons/ha). There were 3
lines having yield of more than one ton/ha i.e. FG2-47-1-3 (2.00 tons), FM1-57-1-2 (1.48 tons) and
FM1R-32-1-1 (1.06 tons) (Table 1). The low yield of the lines and check varieties was due to blast
and bacterial leaf blight and scarce rain during the reproductive period.
Based on the criteria of CGV, then there are two characters that have relatively high CGV,
namely plant height and intensity of neck blast disease; two characters have the medium CGV i.e.
the number of grain per panicle and the percentage of filled grain and number of filled grain per
panicle; and several other characters have low CGV. Murdaningsih et al. (1990) stated that low
CGV showed rather low genetic variability of the characters and was classified as narrow, while the
medium and high value CGV were classed as broad genetic variability. Thus there were 4
characters that have broad genetic variability, and six have a narrow genetic variability.
Broad sense heritability value of the characters observed ranged from 33.4-91.2% (Table
2). According to Stanfield (1983), broad sense heritability values can be grouped into three high
heritability (0.50 <h
2
<1.00), medium heritability (0.20 < h
2
0.50) and low heritability (h
2
<0.20).
Based on the heritability values there are two characters that have moderate heritability (20-50%),
i.e. the number of productive tillers and yield potential. another character has a heritability of 50%
(Table 3). This means that agronomic characters were controlled by genetic factors more than
environmental factors. Selection will be effectively carried out for characters with high heritability
value.

Table 2. Variance components, heritability and genetic variability coefficient new plant type of upland rice lines

Characters
2
g

2
p
2
e h
2
bs
(%) CGV (%)
1. Plant height 315.9 357.4 41.4 88.4 17.0
2. Days to harvest 18.8 29.1 10.4 64.4 3.8
3. Number of productive tillers 0.1 0.3 0.2 44.3 2.0
4. Number of filled grain per panicle 5.6 9.7 4.1 57.5 10.0
5. Number of spikelet per panicle 3.0 4.1 1.1 73.0 5.3
6. Percentage of filled grain 3.7 6.8 3.1 55.0 9.2
7. The 1000-filled grain weight 9.0 9.9 0.9 91.2 5.7
8. Yield 0.04 0.1 0.1 33.4 1.9
9. Intensity of leaf blast disease 3.4 3.6 0.5 95.7 8.4
10. Intensity of neck blast disease 12.4 13.2 2.2 94.4 15.0
Description:
2
g =Genetic variance,
2
p =Phenotypic variance , h
2
bs = broad sense heritability, CGV = Coefficient of genetic
variance .

Line FM2-12-1-2 was blast-resistant but only had yield potential of 0.31 ton per ha. The
line was not tolerant to drought. FG2-47-1-3 line was resistant to leaf blast and neck blast and had
the highest number of productive tillers than all other varieties and lines tested, thus the yield of
FG2-47-13 was also the highest (2 tons/ha). There were ten other lines having yield less than one
ton. Low yield tons was due to low resistance of the lines to leaf blast and neck blast and drought
during reproductive period (Table 3 Location in Bogor).
Based on Dunnett tests the intensity of leaf blast disease in the endemic area in
Sukabumi, of 15 lines tested, there were two lines showing intensity of leaf blast disease not
significantly different from control resistant (Limboto), namely FG2-47-1-3 and FM2-33-1-1 (Table
3). Panicle blast resistance of the 15 lines tested showed that the lines with intensity of neck blast
disease not different from controls resistant (Limboto) were FM1-25-1-1, FM1-25-1-2, FG2-47-1 -3,
FM2-12-1-1, and FAT-4-1-2 (Table 3). Line showing both resistance to leaf blast and neck blast was
FG2-47-13.

th
Table 3. The scale and intensity of leaf blast and neck blast in lines of upland rice in Bogor and Sukabumi

Lines Bogor Sukabumi
Leaf Blast Neck Blast Leaf Blast Neck Blast
S I (%) S I (%) S I (%) S I (%)
FG1-66-2-1 5 17.4
aR
9 86.3
aR
7 38.0
aR
9 74.1
aR

FG1R-108-1-1 5 12.6
aR
9 63.3
aR
5 23.4
aR
5 23.5
R

FG1R-51-2-1 5 38.5
aR
9 85.0
aR
5 25.4
aR
7 35.0
aR

FM1-14-1-1 7 57.8
aR
9 97.7
aR
7 55.5
aR
9 87.8
aR

FM1-14-1-2 7 84.8
aR
9 94.7
aR
7 44.8
aR
9 100.0
aR

FM1-25-1-1 3 5.6
T
9 53.0
aR
5 16.2
aR
5 16.8
R

FM1-25-1-2 1 2.9
T
9 73.7
aR
5 19.5
aR
5 13.2
R

FM1-57-1-2 3 4.1
T
5 14.7
R
7 53.2
aR
9 64.4
aR

FM1R-32-1-1 5 45.2
a
9 64.7
aR
5 28.7
aR
7 28.9
R

FM1R-23-1-1 7 50.0
a
9 80.7
aR
5 29.6
aR
9 88.4
aR

FG2-47-1-3 0 0.0
T
1 3.0
T
3 7.8
T
3 5.5
MT

FM1R-19-2-4 7 71.5
a
7 32.7
R
9 62.6
aR
9 96.3
aR

FM2-12-1-1 1 1.1
T
3 6.0
MT
9 66.8
aR
5 18.4
R

FAT-4-1-2 5 20.0
aR
7 49.7
R
7 34.1
aR
1 2.3
T

FM2-33-1-1 - - - - 3 7.5
T
9 77.5
aR

Limboto (a) 0 0.0
T
1 3.7
T
3 4.8
T
1 0.0
T

Note: Figures followed by letter (a) showed higher intensity of blast disease than Limboto (resistant variety), based on the
Dunnett test on a significant level of 5%. I = intensity of the blast disease, T = resistant, R = Susceptible, MT =
Moderate resistant, MR = Moderate susceptible.

Conclusions

There was variability on agronomic traits and blast resistance among the lines evaluated.
FG2-47-1-3 did not have complete characters of NPT, but the line had superior characteristics such
as high percentage of filled grain, medium days to harvest, medium height, medium 1000-filled
grain weight, stay green when harvested and high resistance to blast disease. The population had
high heritability (h
2
bs
) in leaf blast and neck blast resistance, plant height, filled grain per panicle,
days to harvest, number of grain per panicle and 1000-filled grain weight. They showed high
variance coefficient for leaf blast and neck blast resistance, flag leaf length and percentage of filled
grain.

References

Abdullah B, Tjokrowidjojo S, Justianto B, Darajat AA. 2005. Pembentukan padi varietas unggul tipe baru.
Penelitian Pertanian 24(1): 1-7.
[BB Padi] Balai Besar Penelitian Tanaman Padi (2009) Blas Padi. [Tersedia Berkala].
http://bbpadi.litbang.deptan.go.id [November 2009]
Beker B, Zambryski P, Staskawicz B, Dinesh-Kumar SP. 1997. Signalling in plant-microbe interactions. J Sci
276:726-733.
[BPS]. Biro Pusat Statistik. 2005. Statistik Indonesia. 4 hlm.
[Deptan RI] Basis Data Statistik Pertanian 2011. [Tersedia Berkala]. http://www.bps.go.id/tnmn_pgn.php [11
Agustus 2011]. 1 hlm.
Herawati R. 2010. Pembentukan padi gogo tipe baru toleran aluminium dan tahan blas melalui kultur antera
(Disertasi). 162 hlm.
IRRI. 1996. Standard Evaluation System for Rice. International Rice Research Institute, Los Banos, Philippines.
PO. Box. 933, Manila.
Moedjiono, Mejaya MJ. 1994. Variabilitas genetik beberapa karakter plasma nutfah jagung koleksi Balittas
Malang. Zuriat 5(2):27-32.
Murdaningsih HK, Baihaki A, Satari G, Danakusuma T, Permadi AH. 1990. Variasi genetik tanaman padi sawah
di Indonesia. Zuriat 1(1): 32-36.
Peng S, Khush GS, Virk P, Tang Q, Zou Y. 2008. Progress in idiotype breeding to increase rice yield potential.
Review. Field Crops Research 108:32-38.
Prasetyo YT. 2008. Bertanam Padi Gogo Tanpa Olah Tanah. Bibliografi. 69 hlm.
th
Puslitbangtan. 2007. Peningkatan Produksi Padi Menuju 2020. Puslitbang Tanaman Pangan. 7 hlm.
Safitri H. 2010. Kultur antera dan evaluasi haploid ganda untuk mendapatkan padi gogo tipe baru (Tesis).
61hlm.
Scardaci SC et al. 1997. Rice Blast: a new disease in California. J Agr Fact Sheet Ser 1:2-5.
Stanfield WD. 1983. Theory and Problems of Genetics, 2
nd
edition. Schains Outline Series. Mc. Grow Hill Book
Co. New Delhi. 304p.

th
Functional Analysis of Drought-Induced OsLEA3 Promoter
Isolated from Batutegi Rice Cultivar

Agus Rachmat
1
, Satya Nugroho
1
, Bernadetta Rina Hastilestari
1
,
Kinasih Prayuni
1
, Sudarsono
2

1.
Research Center For Biotechnology, Indonesian Institute of Sciences
2
Faculty of Agriculture,

[email protected]

Abstract

Drought is the most significant environmental stress in agriculture and many efforts have been made to improve
crop productivity under water-limiting conditions. Improving yield under drought is a major goal of plant breeding.
Late embryogenesis abundant (LEA) proteins have been implicated in many stress responses of plants. It has
been found that LEA genes are a gene family and play important roles in the protection of water stress.
Expression of OsLEA3 is induced by abiotic stresses, including drought and high salinity. The promoter of
OsLEA3 was cloned from Batutegi, Rojolele and Nipponbare cultivars and its function was analyzed in
transgenic Nipponbare plant by a GUS reporter gene. Transient assay was conducted in order to investigate
GUS expression driven by OsLEA3 promoter. OsLEA3 promoter was expressed in embryogenic callus
indicated by the appearance of blue spots. Differences in color produced in embryogenic callus showed different
expression level.

Key words: rice, drought, Batutegi, Rojolele, Nipponbare, GUS, OsLEA3 promoter

Introduction

Rice (Oryza sativa L.) is one of the major staple foods. As the population growth goes up,
the rice production must be increased. However, the field for rice cultivation has decreased because
of the change of paddy field into housing and industry. Moreover, drought influences the rice
production especially in North China and South Asian. Thus, rice becomes one of the target source
of gene and genome sequence analysis project among cereal plants (Goff et al. 2002).
LEA proteins constitute a large group of proteins that specically expressed during seed
development. LEA proteins are located in seeds and pollen. Many vegetative organs can also
express some LEA proteins under conditions of dehydration, osmotic stress, cold or exogenous
ABA. First LEA proteins were identied during the desiccation phases of seed development. These
proteins were reported to protect specic cellular structures or ameliorate the effect of drought
stress by sequestering ions and maintaining minimum cellular water requirements (Hu, 2008).
Plant has physiological and molecular response mechanisms to tolerate drought. Those
mechanisms are osmotic accumulation, scavenging ROS, and osmoprotectant protein production
such as late embryogenesis abundant (LEA) and heat shock protein. LEA gene is identified as an
expresed gene in the late phase of seed growth. Research on LEA genes has showed that LEA 3
gene is responsible for drought tolerance. A major problem under severe dehydration is that the
loss of water leads to crystallization of cellular components during the course of dehydration and
dormancy, which damages cell structures (Spelundm et al 1996). Some of the LEA proteins could
essentially be considered compatible solutes that likely play the role similar to sugars in maintaining
the structure of the cytoplasm in the absence of water (Hu 2008). The goal of this research is to
study the function of LEA3 promoter isolated from rice cv. Batutegi.

th

Promoter OsLEA3
Promoter sequence primers were designed based on sequence of genes LEA3 HVA-like
gene promoter from rice cultivar IRAT 109 (GenBank Acc. DQ837728) and has been adapted to the
BAC sequence of chromosome No. 5 rice cultivar Nipponbare (GenBank Acc. AC104713). Primer
sequences are also designed to include the start codon (ATG) of mRNA sequences LEA3 gene
(GenBank Acc. DQ789359) and the addition sequence EcoRI (G AATTC) and BglII (AGATCT) in
order to add EcoRI and BglII restriction sites in the primers. The predicted promoter was amplified
and isolated by PCR. The amplified fragments were sequenced to ensure fidelity.

Isolation of rice genomic DNA
Isolation of genomic DNA of rice cv. Batutegi was conducted by CTAB method (Saghai-
Maroof et al., 1984) that has been optimized. Rice leaf samples were taken from 1-month-old
plants. A total of 2 g leaf samples were prepared using aluminum foil wrapping. Leaf powder was
put into polypropylene tubes containing 10 ml of buffer solution which has been has been preheated
in the incubator at 65
o
C for 30 minutes.

PCR analysis
All PCR reactions were done using 20 ng DNA template. PCR reaction mix contained 6.5
uL nuclease free water, 12.5 uL Green Go Taq 2x Master, 2.5 uL for each LEA F primer (0.1 M)
and LEA R (0.1 M) promoter LEA3, and 1 l template DNA. PCR conditions were: initial
denaturation 95
o
C for 3 minutes, followed by 35 cycles of denaturation at of 95
o
C for 1 minute,
annealing at 60C for 1 minute, and initial extention at 72
o
C for 1 minute. The cycle was terminated
by final extention at 72
o
C for 10 minutes.

Vector Construction

1.

2.

3.

Figure 1. Vector Construction of OsLEA3 promoter::GUS.

Agrobacterium mediated transformation
Agrobacterium tumefaciens LBA4404 strain was transformed using recombinant plasmid
pC1305 containing hygromycin phosphotransferase gene (hpt) controlled by CAMV 35S promoter,
and GUS gene controlled by OsLEA3 promoter.

pOsLEA3 NB GUS

hpt
Left Border
Right Border
NosT
pOsLEA3 RJ GUS

hpt
p35S
Left Border Right Border
NosT
pOsLEA3 BT GUS

hpt
p35S
Left Border Right Border
NosT
p35S
th
Histochemichal GUS assay
Water deficit treated and non treated plant tissues were vacuum infiltrated for 1 h in the
GUS reaction mixture containing 1 mM 5-bromo-4-chloro-3-indolyl- b-D-glucuronide (X-gluc) and 50
mM sodium phosphate buffer and incubated at 37
o
C overnight. The reaction was stopped by adding
75% ethanol, and the pigments and chlorophylls were removed by repeated ethanol treatment.


Amplification of OsLEA3 promoter
Isolation of 1.291 bp OsLEA3 gene promoter was conducted by amplification of DNA
genome using PCR with specific primers and visualized with 0.8% agarose gel (Figure 2). The
PCR fragment was then cloned into pGEM-T Easy and then used to construct pC1305 based
recombinant plasmid.

Figure 2. Amplification of OsLEA3 promoter.

Verification of the recombinant pGEM-T plasmid was conducted using EcoRI restriction
analysis . The result showed 3 fragments, which were fragment with size 3.001 bp (pGEM-T Easy
vector plasmid), 1.291 bp (gene OsLEA3 promoter), and 12 bp (nucleotides between EcoRI site of
OsLEA promotor gene and EcoRI site of pGEM-T Easy) fragments (Figure 3).

Figure 3. Electrophoresis of recombinant vector digested with EcoRI.

Rice Transformation using Agrobacterium
Recombinant vector containing OsLEA3promoter was successfully constructed and
trasformed to rice cv. Nipponbare. Selection of Transformed plants was selected on hygromisin
contained medium.
th

Figure 4. Successfull transformed plant in the selection medium.

Some transformed calli survived in medium containing hygroimisin. Hygromisin resistant
celli were subcultured to regeneration medium. Calli with green spot grew into planlets. Table 1
showed low transformation efficiency. It needs to be increased by optimizing conditions of the
culture. Factors that influence the low efficieny of transfomation are method of tranformation, type of
explants and condition of culture.

Table 1. Genetic transformation of OsLEA3 ::GUS to rice cv. Nipponbare

Histochemical Assay
Transient expression assaysof OsLEA3::GUS promoter of rice cv. Nipponbare, Rojolele
and Batutegi were successfully conducted. GUS gene expression was identified with blue spot on
the transformed calli .Figure 5 showed the difference intensity of blue spot in three cultivars. It
means that the expression level of GUS gene differ among different OsLEA3 promoters. Real Time
PCR will be conducted for further qualitative analysis.

Figure 5. Histochemical assay of transformed calli, NB= Niopponbare, RJ= Rojolele, BT= Batutegi.

Conclusion

1. Recombinant plasmid pCambia1305 of OsLEA3::GUS of Batutegi, Rojolele and Nipponbare
cultivars was succesfully constructed.
2. Promoters OsLEA3 of Batutegi, Rojolele and Nipponbare cultivars controlled GUS expression
differently among those cultivars
No Recombinant vectors Rice Varieties infected calli GUS
assay
Number of
Planlets
1. OsLEA3 NB:: GUS Nipponbare 600 Positive 32
2. OsLEA3 Rj:: GUS Nipponbare 600 Positive 19
3. OsLEA3 BT:: GUS Nipponbare 600 Positive 7
th
References

Bray, E. A. 1993. Molecular response to water deficit. Plant Physiology 103: 1035-1040.
Gao, J-P., D-Y. Chao & H-X. Lin. 2007. Understanding abiotic stress tolerance mechanisms: Recent studies on
stress response in rice. Journal of Integrative Plant Biology 49(6): 742--750.
Goff, S. A. et al. 2002. A draft sequence of rice genome (Oryza sativa L. ssp. Japonica). Science 296: 92--100.
Kalefetolu, T. & Y. Ekmeki. 2005. The effects of drought on plants and tolerance mechanisms. Fen Bilimleri
Dergisi 18(4): 723--740.
Promega. 2007. Technical manual pGEM-T and pGEM-T Easy vector systems. Promega Corporation, Madison:
1--28 hlm.
Spelundm, S., Aeboelarssen, S., Hughes, D.W., Galau, G.A.,Larsen, F., and Jakobsen, K.S., 1992. Late Embryo
Genesis Abundant Genes Encoding Proteins with Different Numbers of Hydrophilic Repeats Are
Regulated Differentially by Abscisic Acid and Osmotic Stress, Plant J. vol. 2, pp. 241252.
Sambrook, J. & D.W. Russel. 2001. Molecular cloning: A laboratory manual, vol 1-3. 3rd ed. Cold Spring Harbor
Laboratory Press, New York. 94 hlm.
Hu T. Z. 2008. OsLEA3, a Late Embryogenesis Abundant Protein Gene from Rice, Confers Tolerance to Water
Deficit and Salt Stress to Transgenic Rice. Russian Journal of Plant Physiology, Vol. 55, No.4, pp. 530
537.
Xiao, B., Y. Huang, N. Tang, & L. Xiong. 2007. Over-expression of a LEA gene in rice improves drought
resistance under the field condition. Theory Application Genetics 115: 35--46.

th
Evaluation of the Nutritional Environment for Rice in Cianjur, Indonesia
for Development of an Advanced Basin Model for Asia

Koki Homma
a,*
, Gunardi Sigit
b
, Handarto
c
, Masayasu Maki
d
, Chiharu Hongo
e
, Koshi
Yoshida
f
, Kazuo Oki
g
, Hiroaki Shirakawa
h
, Tatsuhiko Shiraiwa
a
, Ritsuko Hara
a
, Mitsuo
Kambayashi
a
, Yoshihiro Hirooka
a
, Hiroki Iwamoto
a

a
Graduate School of Agriculture, Kyoto University, Kyoto, Japan

b
Regional Office of Food Crops Service West Jawa Province, Indonesia
c
Human Resource Development, Universitas Padjadjaran, Indonesia

d
Graduate School of Global Environmental Studies

e
Center for Environmental Remote Sensing, Chiba University

f
Collage of Agriculture, Ibaraki University

g
Institute of Industrial Science, the University of Tokyo

h
Graduate School of Environmental Studies, Nagoya University
* Corresponding author: Graduate School of Agriculture, Kyoto University, Sakyo-ku, 6068502, Kyoto, Japan.
Tel.: +81 75 753 6042; fax: +81 75 753 6065.
[email protected]

Abstract

Food production systems in tropical Asia face the following problems: 1) increased demand for production; 2)
increasing environmental load; 3) water scarcity and 4) effects of climate change. To overcome these problems,
strategies for better management of crop and environmental resources are recommended. Here, we describe
our research in Cianjur, Indonesia under the project Development and Practice of Advanced Basin Model in
Asia Toward Adaptation to Climate Change. The study area, Cianjur, is one of the main rice production areas
in Indonesia, and has water reservoirs that supply water to Jakarta. However, excess nutrients from agricultural
land cause environmental problems. In this situation, evaluation of the nutritional environment for rice growth is
necessary. We have begun to evaluate the nutrient concentrations in the irrigation water, soil and plants. The
relationships of these nutrient contents to rice growth were analyzed using a rice growth simulation model. The
simulation model and remote-sensing technologies were used in combination to evaluate the geographic
distribution of rice growth and nutritional environment. The research produced baseline information for
developing the Advanced Basin Model.

Keywords: environmental problem, irrigation water, remote-sensing, simulation model, soil solution

Introduction

Food production systems in tropical Asia face the following problems: 1) increased
demand for production; 2) increasing environmental load; 3) water scarcity and 4) effects of climate
change. To overcome these problems, strategies for better management of crops and
environmental resources are recommended.
Since the green revolution, modern agricultural technology has increased land productivity
and supported population growth. However, this technology tends to institutionalize agricultural
management and reduce diversity. Previous studies reported that such institutionalized
management increased the risk of disasters. Tsuno (1995) analyzed cold summer damage to rice
production in Japan in 1993 and concluded that the simplification of management in cultivars and
cultivation methods increased the extent of damage. Shiraiwa et al. (2002) analyzed the variability
of rice production in Thailand and concluded that the annual variation was larger in an intensive
high yielding area (the Central Plain) than in an extensive low-yielding area (the Northeast).
Yoshino et al. (2000) analyzed the relationship between the Southern Oscillation Index and rice
production in Indonesia and reported that the negative effect was largest in Java, which was the
th
most productive area. These examples indicate that the present management is insufficient for
coping with unfavorable conditions. Management variability may thus be the key to attaining
production stability.
The high fertilizer input required by modern agriculture technology often exceeds an
acceptable amount in the field and increases the environmental load. To optimize the input, the
available nutrients in the soil and the requirements of the plant should first be evaluated. Because
water scarcity is predicted in the future, the available water supply should also be evaluated.

The project Development and Practice of Advanced Basin Model in Asia Toward
Adaptation to Climate Change

As mentioned above, the present situation demands not only a production increase, but
also management optimization based on resource evaluation. Because the smallest water
management unit is a basin and nearly all excess nutrients move with the water stream in the basin,
a strategy to overcome these problems must be developed at the basin scale. Here, we established
the project Development and Practice of Advanced Basin Model in Asia Toward Adaptation to
Climate Change supported by the Ministry of the Environment, JapanThe project includes the
evaluation of environmental resources and crop production, proposals for better management and
also the establishment of an environmental conservation community. The Citarum River in
Indonesia and the Num Ngum River in Laos were selected as test sites (Oki, 2011). This
manuscript describes one of the project activities in Indonesia, which were managed by the lead
author. In the activities, the nutrient concentrations of the irrigation water, soil solution and plants
are evaluated their relationships to rice growth will be analyzed using a rice growth simulation
model. The relations in terms of rice growth would be analyzed by using rice growth simulation
model. The simulation model and remote-sensing technologies will be used in combination to
evaluate the geographic distribution of rice growth and then nutritional environment.

Overview of research area and activities

The research area is in the hydrographic basin of the Citarum River in West Java,
Indonesia. The basin includes Bandung, the third largest city in Indonesia, and a total of 5 million
people live in the area (Fig. 1a). Because the river is heavily polluted by human sewage and
agriculture, the Asian Development Bank has called it the worlds dirtiest river and approved a loan
for clean-up in 2008. The river has 3 dams and one of 3 dams directly supplies water for Jakarta;
thus clean-up of the river is of urgent concern.
Field observations have been conducted in the Bojongpicung and Ciranjang districts,
Cianjur regency, West Java. The area is located between the Saguling and Cirata reservoirs and is
downstream of Bandung. We selected 40 paddy fields, of which 30 were planted with rice and 10
were planted with soybeans in August 2011 (Fig. 1b). In addition to the chemical properties of the
soil, the nitrogen and phosphate concentrations of soil solutions are periodically monitored.
Because the nutrient concentrations in irrigation water are also measured along 3 points in the
major channels, the nutritional environment for crop growth can be assessed in terms of nitrogen
and phosphate levels.
Plant growth is nondestructively evaluated in terms of plant height and canopy cover using
a digital camera. The spectral reflectance of the canopy is measured once a week with a
reflectance-measuring instrument (MS-720, Eiko seiki Co. Ltd.). The plants are also destructively
sampled once per month to determine the leaf area index (LAI), above-ground dry matter and root
density. The grain yield and above-ground biomass will be measured at maturity.

th
b)
Bandung
Cianjur
Jatilful
Cirata
Sagling
a)
Jakarta

b)

We selected 30 rice fields from 6 locations () and 10 soybean fields from 2 locations (o). Irrigation water is periodically
monitored at 6 locations for rice fields.

Figure 1. Maps of the hydrographic basin of the Citarum River (a) and the field observation site (b).

Strategies for analysis and evaluation

To develop strategies for managing crop production in the hydrographic basin, the
geophysical distribution of environmental resources and crop growth must be evaluated. However,
the data we obtain are point-based. Accordingly, a method that scales up from point to area is
needed. Satellite-based remote-sensing can be used for this purpose, and one of the co-authors of
this paper had already developed a method that has been adapted in an agricultural area of Japan
(Nuarsa et al. 2011). However, obtaining satellite images for analysis is difficult because the area
often obscured by clouds.
To compensate for the missing data, we employed a simulation model. The authors
developed the simulation model to predict rice growth and yield under rainfed conditions based on a
field survey in Northeast Thailand, where the water and nutrients are quite limited (Fig. 2; Homma
and Horie, 2008). Because the model was modified from SImulation Model for RIce Weather
relations (SIMRIW), which has a good reputation for predicting the effects of climate change on rice
production (Horie et al. 1995), the modified model may be able to handle climate change issues for
the advanced basin model. We are now developing a simulation model to use in combination with
remote-sensing (Fig. 3; Maki and Homma, 2011). The combined model will be used to evaluate the
nutritional environment and predict rice yield by correcting the simulated data with satellite-based
remote-sensing data. The combined model may also help to analyze the relationship between the
remote-sensing data and field observations. The analysis will first be used for rice production and
may be expanded to examine green soybean (edamame) production.
th

The basic concept of the model is derived from SIMRIW (SImulation Model for RIce Weather relations, Horie et al. 1995), and
modified for rainfed rice production in Northeast Thailand (Homma and Horie, 2008).

Figure 2. Schematic illustration of the rice growth simulation model.

Figure 3. Examples of leaf area index (LAI) simulated by the rice growth simulation model and corrected by
remote-sensing (Maki and Homma, 2011).

th
Conclusions

Here, we describe one of our activities in Cianjur, Indonesia. To develop better
management practices for overcoming environmental problems and adapting to climate change,
evaluation of the nutritional environment and rice growth are necessary. For this purpose, we have
begun to evaluate the nutrient concentrations of irrigation water, soil solutions and plants. The
relationship between these nutrient concentration and rice growth will be analyzed using a rice
growth simulation model. The simulation model and remote sensing technologies will be used in
combination to evaluate the geographic distribution of nutritional environment and rice growth.

Acknowledgement

The project is supported by the Environment Research and Technology Development Fund, Ministry
of the Environment, Japan (E1104).

References

Homma K and T Horie. 2008. The present situation and the future improvement of fertilizer applications by
farmers in rainfed rice culture in Northeast Thailand. In: LR Elsworth and Paley WO (Eds.) Fertilizers:
Properties, Applications and Effects. Nova Science Publishers, N.Y. 147-180.
Horie T, H Nakagawa, HGS Centeno and M Kropff 1995. The rice crop simulation model SIMRIW and its testing.
In Modelling the Impact of Climate Change on Rice in Asia (Matthews, R. B. et al. eds.), CAB
International, Oxon, UK. p.51-66.
Maki M and K Homma 2011. Development of Simulation Model to Evaluate Geographical Distributions of Rice
Growth and Yield in Relation to Weathers, Varieties and Fields. Proc. Annual Meeting of Society of
Environmental Science, Japan in 2011.
Nuarsa IW, F Nishio and C Hongo. 2011. Spectral characteristics and mapping of rice plants using multi-
temporal landsat data. J. Agric. Sci. 3: 54-67.
Oki K. 2011. Development and Practice of Advanced Basin Model in Asia. Proc. Annual Meeting of Society of
Environmental Science, Japan in 2011.
Shiraiwa T, H Nakagawa, T Horie, T Matsui and K Homma. 2001. Variability in rice production and precipitation
in Thailand. Chikyukankyo 6: 207-215. (in Japanese)
Tsuno Y. 1995. Clarification of actual situation and cultivation management problem in cool summer damage on
rice production in Japan in 1993. Research Project Number 06304012. Research Report of Grants-in-Aid
for Scientific Research, MEXT and JSPS, Japan. Pp. 233. (in Japanese)
Yoshino M, K Urushibara,-Yoshino, W Suratman. (2000) Agricultural production and climate change in
Indonesia. Global Environ. Res. 3: 187-197.

th
The Nutritional Environment in Nonfertilized Rice Production and Its Effect
on the Nutritional Quality of Brown Rice

Ritsuko Hara
a
, Koki Homma
a *
, Yoshihiro Hirooka
a
, Mitsuo Kuwada
ab
and Tatsuhiko
Shiraiwa
a

a
Graduate School of Agriculture, Kyoto University, Kyoto, Japan.
b
NPO Nonorganic, Nonchemical Crop Production Research Group, Kyoto, Japan.
Tel.: +81 75 753 6042; fax: +81 75 753 6065.
[email protected]

Abstract

The nonfertilized-nonchemical crop production (so-called nature farming) proposed by Mr. Mokichi Okada is a
popular farming method in both Japan and worldwide. The farming method uses neither fertilizers nor chemicals
but obtains comparable yields to those produced by conventional farming. Although the method was designed to
utilize natural resources, the details of the mechanism are still unknown. This study was aimed to evaluate the
nutritional environment on the basis of the measurement of the nutrients in the soil solution and to analyze the
effect on the nutrient concentrations of brown rice. For this purpose, we selected 2 nonfertilized-nonchemical
paddy fields (NN fields) and 1 experimental paddy field (Expt field) as a reference. One of the NN fields was
cultivated for 6 years without fertilizer (6-year NN), and another was cultivated in this way for 59 years (59-year
NN). In the Expt field, 3 types of fertilizer treatments (None, Basal and Conventional) were conducted. The NH
4
+

concentrations in the 6-year NN fields was lower than those in the fertilizer-applied plots (Basal and
Conventional), but they were comparable to that in the None treatment. Conversely, NH
4
+
was not detectable in
the 59-year NN field. Other nutrients were extremely different between the NN fields and Expt field, namely, the
fertilizer treatments (Basal and Conventional) had little effect on the nutrient concentration of the soil solution.
The P
2
O
5
and K
+
levels in the Expt fields were notably higher than those in the NN field, whereas Ca
2+
and Mg
2+

showed an opposite trend. Significant interactions of the genotype by environment were observed for the
nutrient concentrations in brown rice. The relatively low NH
4
+
and K
+
level in the soil solution in the NN fields
tended to result for brown rice in low concentrations of those nutrients, which Japanese people tend to prefer.
The relationship between the nutritional environment and the uptake and concentration of nutrients in brown rice
should be studied further.

Keywords: rice, nonfertilized-nonchemical crop production, soil solution, nutritional quality of rice

Introduction

Agrochemicals such as fertilizers and pesticides largely increase agricultural production and
support the huge population of the world. However, excess inputs of agrochemicals leak into the
environment and cause various kinds of problems that pose threats to human life (Reichenberger et
al. 2007). Organic farming or nature farming is derived from the reactions against such
agrochemical agriculture.
The nonfertilized-nonchemical crop production proposed by Mr. Mokichi Okada is popular in
both Japan and worldwide. This method of farming uses neither fertilizers nor chemicals but obtains
comparable yields to those produced by conventional farming (Okumura, 2002). Okumura reported
that the sources of some of the nitrogen were irrigation water and biological fixation but that the
majority comes from soil. Although the method of farming was designed to utilize natural resources,
the details of the mechanism are still unknown.
Because crop productivity is restricted by nutrients supplied through soil, an evaluation of
the nutritional environment in the soil is quite important when discussing productivity. In general, the
availability of nutrients for plants is evaluated by chemical analyses. However, the nutritional
th
environment is quite influenced by the temperature, soil moisture and plant uptake and exudates,
which suggests that periodic monitoring of the nutritional environment is required to analyze the
plant response to nutrition and the nutrient availability (Boivin et al., 2002).
When plants take up nutrients from the soil, the procurement does not occur on the surface
of the soil particles but through the liquid phase of the soil (soil solution). Nutrients in their ion forms,
such as ammonium and potassium, move with the soil solution (mass flow) or by diffusion in the
solution. Accordingly, nutritional analyses of the soil solution are suggested to evaluate the
nutritional environment (Smethurst, 2000).
This study investigated nonfertilized-nonchemical fields and an experimental field as a
reference. The soil solutions were sampled once every 2 weeks for the nutritional evaluation. Six
representative rice cultivars were planted to evaluate any cultivar differences in nutrient uptake, dry
matter production, yield and grain quality. This report focused on the changes in the nutrients in soil
solution and the effect on the nutrient content of brown rice.


The experiment was conducted in 2010. We used two types of paddy fields: one was
operated under nonfertilized-nonchemical management by NPO Nonorganic, Nonchemical Crop
Production Research Group (NN fields; Ogura, Uji city, Kyoto Prefecture, 34 54 N, 135 46 E),
and the other was an experimental field in the Graduate School of Agriculture, Kyoto University
(Expt field; Sakyo, Kyoto city, Kyoto Prefecture, 35 02 N, 135 47 E). The NN fields included 2
fields: one was cultivated for 6 years without fertilizer or agrochemicals (6-year NN), and the other
was cultivated for 3 years without fertilizer or agrochemicals after the top-soil was converted using
the soil of a field where nonfertilized-nonchemical management was conducted for 56 years. Thus,
the soil of the converted field was used for a total of 59 years under nonfertilized-nonchemical
management (59-year NN). The experimental year was the 7th and 60th year of cultivation,
respectively. In the Expt field, 3 kinds of fertilizer treatments (None, Basal and Conventional) were
conducted under pesticide application. The none treatment was conducted without fertilizer,
whereas the Conventional and Basal treatments included the application of chemical fertilizer at a
rate of N-P
2
O
5
-K
2
O = 5-5-5 g m
-2
as basal, and the Conventional treatment was top-dressed with
fertilizer on the 22th of July and the 7th of August. The rate of each top-dress application was N-
P
2
O
5
-K
2
O = 2.5-2.5-2.5 g m
-2
. Thus, the total application rate for the Conventional treatment was N-
P
2
O
5
-K
2
O = 10-10-10 g m
-2
. The Basal treatment was designed to starve nutrients around the
heading period.
Based on the results of a study conducted in the same field (Matsuyama et al., 2010), six
representative rice cultivars were selected. Beniasahi (Japan) is a traditional japonica cultivar and
has been self-seed-produced for the 59 years under the nonfertilized-nonchemical management,
suggesting that the cultivar has adapted to these conditions (Okumura, 2002). Nipponbare (Japan)
and Kasalath (India) are standard cultivars of japonica and indica, respectively (Kojima et al., 2005).
Takanari (Japan) is a high-yielding indica cultivar and is promising for the production of rice flour
and as a feed crop. B6144F-MR-6-0-0 (B6144F) was bred for upland cultivation in Indonesia (Atlin
et al., 2006). Bei Khe (Cambodia) is a cultivar that produced the largest amount of dry matter in the
experiment conducted by Matsuyama et al. (2010). The cultivars were sown on the 10th of May and
transplanted to the Expt field on the 3rd of June and to the NN fields on the 8th of June. The
transplanting density was 22.2 hill m
-2
, with 1 plant hill
-1
. The experiment was arranged in a
randomized block design for each field.
A soil solution sampler (DIK-301B, Daiki Rika Kogyo Co., Ltd.) was placed at a 10 cm-depth
in every Nipponbare and B6144F plot. The soil solution was sampled by a syringe aspiration
method once every 2 weeks and the concentrations of NH
4
+
, P, K, Mg and Ca in the solution were
measured. The soil chemical properties were measured by a standard method. The brown rice
th
grains at maturity and the above-ground biomass and leaves at heading were sampled, and its N, K
and Mg concentrations were determined.


Evaluation of the nutritional environment determined on the basis of the soil solution
The three major soil solution nutrients, NH
4
+
, P and K, were quite different among the fields
and treatments (Fig. 1). The NH
4
+
concentration under the Basal and Conventional treatments in the
Expt field was initially quite high due to the effect of the basal fertilizer, but it markedly decreased by
30 days after transplanting. The conventional treatment maintained a relatively higher NH
4
+

concentration due to the top-dress application of fertilizer, whereas the NH
4
+
concentration under
the Basal treatment exhibited a lower level (almost 0 ppm) than the None treatment. The Basal
treatment resulted in nitrogen starvation conditions, as was intended by the experimental design. In
the NN fields, the NH
4
+
concentration in the 6-year NN field peaked at 60 days after transplanting
and maintained levels of approximately 0.70 ppm and 0.25 ppm before and after the peak at 60
days, respectively. The NH
4
+
concentration in the 59-year NN field maintained levels of
approximately 0.2 ppm and 0 ppm for 30 days after transplanting and thereafter, respectively.
3
0 40 80 120
2
1
0
N
H
4
+
c
o
n
c
.

(
p
p
m
)
Days after transplanting
4
5
NN fields
6-year NN
59-year NN
Expt. field
None
Basal
Conventional

0 40 80 120
2
0
P
c
o
n
c
.

(
p
p
m
)
4
6

K
c
o
n
c
.

(
p
p
m
)
12
0 40 80 120
8
4
0

M
g

c
o
n
c
.

(
p
p
m
)
20
0 40 80 120
10
5
0
15

C
a
c
o
n
c
.

(
p
p
m
)
160
0 40 80 120
80
40
0
120

3
0 40 80 120
2
1
0
N
H
4
+
c
o
n
c
.

(
p
p
m
)
4
5
NN fields
6-year NN
59-year NN
Expt. field
None
Basal
Conventional

Figure 1. Change of nutrients concentration in soil solution.
th
The P concentration in the Expt field increased from the transplanting up to 70 days after
transplanting, and differences among the fertilizer treatments were not obvious, suggesting that the
annual P application accumulated P in the soil. Conversely, P was barely detectable in the NN
fields. The difference in the P concentrations between the Expt and NN fields was corresponded to
the soil chemical analysis (data not shown). Although the P concentration in the soil solution was
negligible, the plants took up P from the soil (data not shown). Moreover, although the P
concentration in the soil solution in the 6-year NN field was as low as that in the 59-year NN field,
the P uptake by the plants in the 6 year-NN field was 1.6 times as large as that in the 59-year NN
field. These data suggest that another indicator is required to evaluate the availability of P.
The K concentration was affected by the fertilizer application in the Expt field, but the effect
was short-lived: the baseline concentrations under the Basal and Conventional treatments were
similar to that under the None treatment. The K concentration in NN fields was one half of the basal
concentration in the Expt field, and apparent differences were not observed between the 6-year and
59-year NN fields.
The Ca and Mg concentrations were different at transplanting among the fertilizer treatments
in the Expt field, but the difference disappeared by 30 days after transplanting. The concentration
gradually decreased with time, whereas the concentrations increased until 50 days after
transplanting in the NN fields. The increase was repeated in a flood incubation using the soil
sampled before transplanting (data not shown), suggesting that the trend shown in Fig. 1 is derived
from the characteristics of the soil or the forms of Ca and Mg in the soil.

The effect of nutrients in the soil solution on nutrient concentrations of brown rice
The N and K concentrations in brown rice almost reflected those in the soil solution: the
concentrations of the brown rice in the NN fields tended to be lower than those in the Expt field.
However, the Mg concentration of the brown rice in the 6-year NN field was lower than that under
the Conventional treatment in the Expt field; thus, the concentrations of the brown rice did not
reflect those in the soil solution. The interaction effects of the cultivar and the environment were
significant for all of the nutrients, indicating that the plant responses to the nutritional environment
were different among the cultivars.
Previous studies report that the N concentration in brown rice is affected by that in the flag
leaves at heading (Taira, 1997). The relationship in this study suggests that the indica cultivars are
more affected than the japonica cultivars (Fig. 3). As available data atre inadequate for K and Mg,
the relationship of the K and Mg concentrations of the brown rice was compared with that in the
above-ground biomass at the heading stage. The relationships of the K concentration between the
brown rice and the above-ground biomass were significant for the traditional varieties but not
significant for the improved varieties. The relationships of the Mg concentration between the brown
rice and the above-ground biomass were significant for the traditional indica cultivars but not
significant for the other cultivars (data not shown). As shown in Fig. 3 these cultivar differences may
be one of the causes of the significant interaction of the cultivar and the environment on the nutrient
concentration in brown rice.
In terms of the nutrient concentration of brown rice, 1/N, Mg/K or Mg / (K N) were proposed
as grain palatability indexes for Japan (Nakagawa et al., 2000). As mentioned above, the N and K
concentrations of the brown rice in the NN fields tended to be lower than those in the Expt field,
increasing the indexes in NN fields higher than those in the Expt field. However, as nitrogen
starvation under the Basal treatment apparently decreased the N and K concentrations of the
Nipponbare brown rice, the index for Nipponbare was the highest under the Basal treatment.

th
59-year 6-year None Basal Conv.
Expt. field NN fields
0
1.0
0.5
1.5
N

c
o
n
c
.

(
g

1
0
0
g
1
)
Cultivar**
Environment**
CE**
J Beniasahi
B Nipponbare
3 Takanari
1 B6144F
H Kasalath
F Bei Khe

0
0.2
0.1
0.5
K

c
o
n
c
.

(
g

1
0
0
g
1
)
0.3
0.4
Cultivar**
Environment**
CE**
Expt. Field NN fields

0
0.2
0.1
0.3
M
g

c
o
n
c
.

(
g

1
0
0
g
1
)
Cultivar**
Environment**
CE**
Expt. Field NN fields

0
0.6
0.2
0.8
M
g
/
K

(
g

g
1
)
0.4
Cultivar**
Environment
CE


0
0.5
0
0.2
5
1.0
0
M
g
/
(
K

N
)

(
g

g
1
g
1

)
0.7
5
Cultivar**
Environment**
CE
ns

0
1.0
0.5
1.5
N

c
o
n
c
.

(
g

1
0
0
g
1
)
Cultivar**
Environment**
CE**
J Beniasahi
B Nipponbare
3 Takanari
1 B6144F
H Kasalath
F Bei Khe

Results of ANOVA are shown in the figure:
,
*
,
**
and
ns
indicates 10, 5, 1 % and non- significance, respectively.

Figure 2. Effect of cultivar and environment on nutrition concentration of brown rice (a, b and c), and grain
palatability index (d and e).
th

0.4
1.2
0.8
1.6
B
r
o
w
n

r
i
c
e

(
g

1
0
0
g
1
)
0.5 1.0 1.5 2.0 2.5
Leaf (g 100g
1
)
a) N conc.
Fig. 3 (a)

0.2
0.1
0.5
B
r
o
w
n

r
i
c
e

(
g

1
0
0
g
1
)
0.3
0.4
0.5 1.0 1.5 2.0 2.5 3.0
Above ground biomass (g 100g
1
)
b) K conc.
Fig. 3 (b)
Slope
N conc. P conc.
J Beniasahi 0.30* 0.067**
B Nipponbare 0.18** ns
3 Takanari ns ns
1 B6144F 0.63** ns
H Kasalath 1.01** 0.068**
F Bei Khe 0.66** 0.057**

0.2
0.1
0.5
B
r
o
w
n

r
i
c
e

(
g

1
0
0
g
1
)
0.3
0.4
0.5 1.0 1.5 2.0 2.5 3.0
Above ground biomass (g 100g
1
)
b) K conc.
Fig. 3 (b)
Slope
N conc. P conc.
J Beniasahi 0.30* 0.067**
B Nipponbare 0.18** ns
3 Takanari ns ns
1 B6144F 0.63** ns
H Kasalath 1.01** 0.068**
F Bei Khe 0.66** 0.057**

Figure 3. (a) Relationship between N concentration in leaf at heading and that in brown rice at maturity. (b)
Relationship between K concentration in above-ground biomass at heading and that in brown rice at
maturity.

References

Atlin GN, HR Lafitte, D Tao, M Laza, M Amante and B Courtois. 2006. Developing rice cultivars for high-fertility
upland systems in the Asian tropics. Field Crops Res. 97: 43-52.
Boivin P, F Favre, C Hammecker, JL Maeght, J Delarivire, JC Poussin and MCS Wopereis. 2002. Processes
driving soil solution chemistry in a flooded rice-cropped vertisol: analysis of long-time monitoring data.
Geoderma 110: 87-107.
Kojima Y, K Ebana, S Fukuoka, T Nagamine and M Kawase. 2005. Development of an RFLP-based rice
diversity research set of germplasm. Breed. Sci. 55: 431-440.
Matsuyama H, K Homma, M Kuwada and T Shiraiwa. 2010. Genotypic variation in rice productivity under
nonfertilized-nonchemical management. Research Report in 2009. NPO Nonorganic, Nonechemical
Crop Production Research Group, Kyoto, Japan. P 6-11.
Nakagawa S, Y Tamura and Y Ogata. 2000. Comparison of rice grain qualities as influenced by organic and
conventional farming systems. Jpn. J. Crop Sci. 69: 31-37.
Okumura T. 2002. Rice production in unfertilized paddy field -Mechanism of grain production as estimated from
nitrogen economy-. Plant Prod. Sci. 5:83-88.
Reichenberger S, M Bach, A Skitschak and HG Frede. 2007. Mitigation strategies to reduce pesticide inputs into
ground- and surface water and their effectiveness; A review. Sci. Total Environ. 384: 1-35.
Smethurst P. 2000. Soil solution and other soil analyses as indicators of nutrient supply: a review. Forest Ecol.
Manage. 138: 397-411.
Taira T. 1997. Estimation of nitrogen content of brown rice in rice cultivar Koshihikari at heading time. Jpn. J.
Crop Sci. 66: 706-707.

th
Effect of Slow Release Fertilizer on Yield and Yield Components
in Chinese High-Yielding Rice Cultivars

Toshiaki Kokubo
a
, Akira Miyazaki
b*
, Tetsushi Yoshida
a
, Yoshinori Yamamoto
b
,
Jing Ju
c
and Yulong Wang
c

a
The United Graduate School of Agricultural Sciences, Ehime University, Japan

b
Faculty of Agriculture, Kochi University, Japan
c
Yangzhou University, China
* Corresponding author: Fac. of Agr, Kochi Univ., 200 Monobe-Otsu, Nankoku-shi, Kochi, 7838502 Japan.
Tel & FAX.: +81 88 864 5123.
[email protected]

Abstract

The effect of slow release fertilizer on yield and yield components in Chinese high-yielding rice cultivars were
evaluated and analyzed to avoid over-fertilization in China. Two different types, linear (L) and sigmoid (S)
fertilizer as a nitrogen (N) source were applied at basal dressing, in comparison with split applications of
ammonium chloride (C type). The application of the slow release fertilizer increased the brown rice yield
significantly in Chinese high-yielding cultivars, Yangdao 4 (YD) and Wuyugen 3 (WY), and was more effective at
low N conditions than at high N conditions. Maximum yield was achieved in YD grown at 21 g N m
-2
by S type,
and in HH grown at 21 g N m
-2
by L type. This indicates that about 30 % of N fertilizer could be saved by the
application of the slow release fertilizer. These effects on yield resulted from the increase in sink size (the
number of spikelets m
-2
multiply one grain weight) due to the increase in the number of spikelets m
-2
. The effect
of the S type slow release fertilizer was more effective on the increase in sink size and the number of spikelets
panicle
-1
than that of L type. Grain filling percentage in WY and HH decreased with the increase in sink size,
while it was slight in YD. Therefore, the increase in sink size was important for YD to improve the yield
production. These responses to the N supply were different between YD and WY, suggesting that the optimum
amount of N fertilizer applied should be varied with these cultivars.

Keywords: Chinese high-yielding cultivar, Nitrogen fertilizer application, rice, slow release fertilizer, yield

Introduction

In Jiangsu province in China, one of the representative rice-producing areas, high-yielding
rice cultivars are widely used for breeding and cultivation with applying a large amount of nitrogen
(N) fertilizer more than 30 g m
-2
to achieve high-yield (Peng et al. 2006). These cultivars have large
yield potentials (Amano et al. 1993; Wang et al. 1995; Yao et al. 2000) and require the application
of large amounts of nutrients, especially nitrogen (N). However, an excess fertilizer application
causes not only an increase of costs but also an outflow of nutrients with an environmental burden.
This requires an appropriate management of the fertilizer application and an improvement of
fertilizer use efficiency (brown rice yield / the amount of N fertilizer application) in the rice cultivation.
The method of fertilizer application has been improved by changing the amounts and timings of
fertilizer application (Peng et al. 2006), and by using farmyard manure (Liu et al. 2008) and
supplemental nitrification inhibitor (Huang et al. 1996) to raise the fertilizer use efficiency. As one of
the effective solutions for high fertilizer recovery rate, a slow release fertilizer has been commonly
used in Japan for the rice cultivation. However, there are few studies in Chinese high-yielding
cultivars (Ju et al. 2006). As recent high-yielding cultivars can achieve high yield even in a small
quantity of fertilizer application (Hasegawa 2003; Taylaran et al. 2009), the optimum fertilizer
condition should be examined by using the slow release fertilizer. In this study, effects of different
th
types of the slow release fertilizer on yield in Chinese high-yielding rice cultivars were evaluated
and analyzed to determine effective methods and amounts of N fertilizer application.


Experiments were conducted in 2006 to 2009 (Exp.1) and 2010 (Exp.2) in a paddy field of
Faculty of Agriculture, Kochi University, Japan. Three treatments were designed by types of N
fertilizer applied. Ammonium chloride was applied as conventional N fertilizer (C type) for basal and
top-dressing at each growth stage (basal:20 days after transplanting : 20 days before heading : 10
days before heading : heading = 2 :1:1:1:1). Two types of the slow release fertilizer, linear type (LP
coat 100, L type) and sigmoid type (LP coat SS 100, S type) were applied as basal dressing all at
once, except for the S type in 2006 and 2007, in which both 6 g m
-2
of sigmoid type and 4 g m
-2
of
ammonium chloride were mixed at basal dressing and 2 g m
-2
of ammonium chloride was
additionally applied at 20 days after transplanting to promote early growth. In Exp.1, Chinese high-
yielding Indica cultivar, Yangdao 4 (YD), Chinese high-yielding Japonica cultivar, Wuyugen 3 (WY)
and conventional Japonica cultivar, Hinohikari (HH) were grown at the rate of 12 g N m
-2
for each
types of N fertilizer. In Exp.2, three different amounts of N, 12, 21, 30 g m
-2
for each type of fertilizer
were applied in YD and HH. The same amounts of P
2
O
5
and K
2
O as N in both experiments were
applied at basal dressing and at each growth stage (basal : 20 days before heading : 10 days
before heading =4:1:1), respectively. All treatments were arranged with 2 replications by a
randomized block design. Yield and yield components were determined by using 20 hills sampled at
maturity.


The effect of the slow release fertilizer on brown rice yield
Brown rice yield significantly increased with the application of slow release fertilizer in
Exp.1 (Table 1). The effect of the slow release fertilizer on yield did not differ significantly among
cultivars, but the average increasing percentage in YD and WY (6 to 15%) was higher than that in
HH (0 to 5%). This result agreed with reports by Sato et al. (1993; 1997) in which the yield
increased by 33 to 55% and 12 to 14% respectively.
The effect of the slow release fertilizer on yield was not significant in Exp.2 (Table 2).
However, the increasing percentage at 12 g N m
-2
was higher than that at 30 g N m
-2
in both
cultivars, showing that the slow release fertilizer was more effective on yield in low N fertilizer
conditions than in high N fertilizer conditions. In addition, this effect was significantly different
between cultivars, and the increasing percentage in YD was higher than that in HH. Maximum yield
was obtained in YD grown at 21 g N by S type (781 g m
-2
), and in HH grown at 21 g N by L type
(539 g m
-2
), which were higher than those grown at 30 g N by C type. This result indicates that the
slow release fertilizer saves about 30% of N fertilizer applied, compared with the conventional
fertilizer.
th
Table 1. Yield and yield components of rice cultivars in Exp.1 (the average value of 2005-2009)

Note: Italic values indicate the increasing percentage by the slow release fertilizers.
Values with different small letters indicate significant differences at the 5% level among methods of the fertilizer application
and cultivars.
Values with different capital letters indicate significant differences at the 5% level among varieties.
*, **, ***; Significant at 5, 1, 0.1% levels by ANOVA, respectively; ns is Not significant.

Analysis of yield components
These effects of the slow release fertilizer on yield resulted from the increase in sink size
(the number of spikelets m
-2
multiply one grain weight, Venkateswarlu and Visperas, 1987) due to
the increase in the number of spikelets m
-2
in both experiments, although 1000 grain weight
significantly decreased with the increase in the number of spikelets m
-2
(Table 1, 2). The increase in
the number of spikelets m
-2
was attributed to the increase in both the number of panicles m
-2
and
the number of spikelets panicle
-1
. The effect of the S type slow release fertilizer was more effective
on the increase in sink size and the number of spikelets panicle
-1
than that of L type. Kamekawa
(1990) reported that sink size increased with the application of the slow release fertilizer of linear
type mainly due to the increase in the number of panicles m
-2
in Japanese cultivars. These results
show that there is a difference of the effect on the yield components between L and S types.
The increase in sink size resulted in the decrease in grain filling percentage in both
experiments. However, Tanaka (1988) and Nakanishi et al. (1990) reported that grain filling
percentage increased despite the increase in the number of spikelets m
-2
with applying the slow
release fertilizer at panicle neck-node differentiation stage. This result may be because of late
fertilizer application in comparison with our study.
A negative relationship between sink size and grain filling percentage was observed in WY
and HH (P<0.10), but not observed in YD in Exp.1 (Figure 1A). A similar trend was observed in
Exp.2; the decrease in grain filling percentage in YD was less than that in HH when grown with high
N fertilizer conditions (Figure 1B). Yang et al. (2002) reported that grain filling percentage in recent
Chinese cultivars did not always decrease with the increase of the number of spikelets panicle
-1
.
These results show that YD maintains high grain filling percentage with high sink size in response to
high N conditions, resulting in high fertilizer use efficiency. However, Chinese high-yielding
Japonica cultivar, WY had a different trend with YD, and showed the significant decrease (P<0.10)
in grain filling percentage with the increase in sink size. This indicates that the optimum amount of
fertilizer application should be different between YD and WY.

th
Table 2. Yield and yield components of rice cultivars in Exp.2 (2010)

Note: Italic values indicate the increasing percentage by the slow release fertilizers.
Values with different small letters indicate significant differences at the 5% level among methods of the fertilizer
application and cultivars.
Values with different capital letters indicate significant differences at the 5% level among varieties.
*, **, ***; Significant at 5, 1, 0.1% levels by ANOVA, respectively; ns is Not significant.

YD: y = -0.0305x + 98.9
r = -0.754 ***
HH: y = -0.0854x + 124.8
r = -0.792 ***
0
20
40
60
80
500 700 900 1100 1300 1500
Sink size (g m
-2
)
G
r
a
i
n

f
i
l
l
i
n
g

p
e
r
c
e
n
t
a
g
e

(
%
)Yield
900 g m
-2
700 g m
-2
500 g m
-2
300 g m
-2
100 g m
-2 HH: y = -0.032x + 100.0
r = -0.366
WY: y = -0.0258x + 98.3
r = -0.399
50
60
70
80
90
500 700 900 1100
Sink size (g m
-2
)
G
r
a
i
n

f
i
l
l
i
n
g

p
e
r
c
e
n
t
a
g
e

(
%
)
YD: r = 0.167 n.s.
Yield
900 g m
-2
700 g m
-2
500 g m
-2
YD WY HH
C
L
S
(A) (B)

***, ; Significant at 0.1 % and 10 % levels, respectively. n.s.; Not significant.

Figure 1. Relationship between sink size and grain filling percentage in Exp.1 (A) and Exp.2 (B).

th
Yearly differences
The effect of the slow release fertilizer on yield was minimum in 2006 (-1%) and maximum
in 2009 (12%) on average of cultivars in Exp.1. This yearly differences of the slow release fertilizer
was because of the decreasing rate in grain filling percentage and the increasing rate in sink size
due to the increase in the number of spikelets panicle
-1
. That is, the remarkable decrease in grain
filling percentage and the slight increase in sink size were observed in 2006, while the opposite
trend was observed in 2009.

Conclusion

From the above results, the application of the slow release fertilizer increased the brown
rice yield significantly, especially in YD and WY, and was more effective at low N fertilizer conditions
than at high N fertilizer conditions. Maximum yield was achieved in YD grown at 21 g N m
-2
by S
type, and in HH grown at 21 g N m
-2
by L type. Therefore, about 30% of N fertilizer could be saved
by the application of the slow release fertilizer without any decrease in yield, in comparison with the
conventional fertilizer. This resulted from the significant increase in sink size due to the increase in
the number of spikelets m
-2
. The slow release fertilizer of S type was more effective on increases in
sink size and the number of spikelets panicle
-1
than that of L type. The increase in sink size resulted
in the decrease in grain filling percentage in WY and HH, while it was negligible or slight in YD,
which contributed to the increase in the yield production. These responses to the N supply were
different between YD and WY, both Chinese high-yielding cultivars. Therefore, the amount of N
fertilizer applied should be varied with these cultivars.

References

Amano T, Qingsen Z, Yulong W, Naoto I and Hidehiko T. 1993. Case studies on high yields of paddy rice in
Jiangsu province, China: I. Characteristics of grain production. Jpn. J. Crop Sci. 62: 267-274.
Hasegawa H. 2003. High-yielding rice cultivars perform best even at reduced nitrogen fertilizer rate. Crop Sci.
43: 921-926.
Huang W-Y, David S and Irwin TH. 1996. On-farm costs of reducing residual nitrogen on cropland vulnerable to
nitrate leaching. Rev. Agric. Econ. 18: 325-339.
Liu J, Qiufa X, Qinghua S and Muying L. 2008. Rice uptake and recovery of nitrogen with different methods of
applying
15
N-labeled chicken manure and ammonium sulfate. Plant Prod. Sci. 11: 271-277.
Ju J, Yoshinori Y, Akira M, Tetsushi Y and Yulong W. 2006. Effects of the amount and the kinds of fertilizer on
the bleeding rate and nitrogen absorption in a Chinese high-yielding cultivar, Yangdao 4. Jpn. J. Crop Sci.
75: 249-256.
Kamekawa K. 1990. LP fertilizer - characteristic of fertilizer effect and utilization- in Nougyou gijyutsu taikei 2-2,
Noubunkyo eds., Tokyo, Japan, Gi 522: 38-43.
Nagata K, Satoshi Y, Jun-ichi T and Tomio T. 2001. Effects of dry matter production, translocation of
nonstructural carbohydrates and nitrogen application on grain filling in rice cultivar Takanari, a cultivar
bearing a large number of spikelets. Plant Prod. Sci. 4: 173-183.
Nakanishi M, Nobuyuki T and Ho A. 1990. Effect of coated urea topdressing on growth and yield of rice plant.
Jpn. J. Crop sci. 59: 265-269.
Peng S, Roland JB, Jianliang H, Jianchang Y, Yingbin Z, Xuhua Z, Guanghuo W and Fusuo Z. 2006. Strategies
for overcoming low agronomic nitrogen use efficiency in irrigated rice systems in China. Field Crops
Research. 96: 37-47.
Sato T, Kyoichi S, Masagiko S and Tokuro A. 1993. Single basal application of total nitrogen fertilizer with
controlled-release coated urea on non-tilled rice culture. Jpn. J. Crop Sci. 62: 408-413.
Sato T, Kyoichi S and Masahiko S. 1997. A single basal application of controlled-release coated urea to rice
cultures using pot seedlings in a cool region. Jpn. J. Crop Sci. 66: 11-16.
Tanaka N. 1988. Topdressing of coated urea to rice plant for saving of labor. Jpn. J. Soil Sci. Plant Nutr. 59:
500-503.
th
Taylaran DR, Satomi O, Naoko M, Taiichiro O, Takashi M and Tadashi H. 2009. Performance of a high-yielding
modern rice cultivar Takanari and several old and new cultivars grown with and without chemical fertilizer
in a submerged paddy field. Plant Prod. Sci. 12: 365-380.
Venkateswarlu B and Visperas RM. 1987. Source-sink relationships in crop plants. IRRI Rice Research Paper
Series 125: 1-19.
Wang Y, Yoshinori Y and Youji N. 1995. Analysis of the factors of high yielding ability for a Japonica type rice
line, 9004, bred in China : I. Comparison of yielding ability with a Japanese rice variety under the same
level of spikelets number per area. Jpn. J. Crop. Sci. 66: 1-10.
Yang J, Shaobing P, Zujian Z, Zhiqin W, Romeo MV and Qingsen Z. 2002. Grain and dry matter yields and
partitioning of assimilates in Japonica/Indica hybrid Rice. Crop Sci. 42: 776-772.
Yao Y, Yoshinori Y, Yulong W, Tetsushi Y, Akira M, Youji N, and Cai J. 2000. Macro-element absorption at
maturity in relation to grain Yield in high-yielding rice cultivars. Soil Sci. Plant Nutr. 46, 815-824.

th
Drought Resistance of NERICA Compared with Asian Rice,
African Rice and Millets in the Field with Different Fertilization Levels

Michihiko Fujii
a,*
, Seiji Ishihara
a
, Ryohta Shinohara
a

a
Faculty of Education, Shizuoka University, Shizuoka, Japan
* Corresponding author: Faculty of Education, Shizuoka University, 836, Ohya, Shizuoka, 422-8529, Japan.
Tel.: +81 54 238 4680; fax: +81 54 238 4680.
[email protected]

Abstract

Recently NERICA (New Rice for Africa) was developed by a crossing between African rice (Oryza glaberrima
Steud.) with Asian rice (Oryza sativa L.) in West Africa, and is considered to be drought resistant, but it is not
clarified enough about the difference in reactions under dry condition. In this research, NERICA, Asian rice,
African rice and millets were cultivated in the field under drought condition with different fertilization levels to
compare dry matter production, stomatal and leaf characteristics and water absorbing characteristics to comfirm
the characteristics of NERICA under drought condition. Fertilization levels were 6gN/m
2
in standard fertilization
level and 2gN/m
2
in low fertilization level. Stomatal conductance was measured by porometer and soil water
contents at individual depths (0-60cm) were measured by TDR method. Leaf thickness was measured by
micrometer and and SPAD value was determined with SPAD meter. In standard fertilization level under drought
condition, top dry weight at harvest was high in Dular, drought resistant Asian rice cultivar. Dry weight at harvest
in low fertilization level tended to be higher than that grown in standard fertilization level. In low fertilization level
one of NERICA showed high dry weight. Dry weight of glaberrima parent of NERICA was high in both standard
and low fertilization levels, but proportion of dead leaf was high. In standard fertilization level, Dular showed
highest stomatal conductance followed by sativa parent of NERICA and one of NERICA. In low fertilization level
sativa parent of NERICA, Dular and one of NERICA showed high stomatal conductance and it tended to be
higher than in standard fertilization level. Glaberrima parent of NERICA showed low stomatal conductance in
both fertilization levels. Average soil water content at 0-60cm depth before harvest in standard fertilization level
was low in Dular followed by glaberrima parent of NERICA. In low fertilization level soil water content was
maintained highest in one of NERICA. Soil water content at 0-20 cm depth in standard fertilization level was low
in glaberrima parent of NERICA. There was large cultivar differences in soil water content at 40-60 cm depth
and soil water decreased significantly in Dular in standard fertilization level. On the contrary it was maintained
highest in one of NERICA in low fertilization level. Dry weight was high in Dular, but soil water content
decreased especially in the standard fertilization level. On the contrary, dry weight was high in one of NERICA
and soil water content was maintained high especially in low fertilization level and at deep soil layer (40-60 cm
depth). There was a significant correlation (r=0.907
**
) between average stomatal conductance and dry weight at
harvest except glaberrima parent of NERICA. In low fertilization level stomatal conductance and dry weight at
harvest tended to be larger than in standard fertilization level. There was a significant correlation (r=0.892
**
)
between average leaf thickness and dry weight at harvest except glaberrima parent of NERICA and cultivar with
thick leaf tended to maintain high dry matter production. There was a significant correlation (r=0.828
**
) between
average leaf thickness and SPAD value in rice. In one of NERICA leaf thickness and SPAD value were higher in
low fertilization level than in standard fertilization level. SPAD value tended to be low in Dular. High leaf
thickness and SPAD values seem to be effective to maintain dry matter production under limited water condition
with high water use efficiency. NERICA seems to be appropriate for the cultivation under drought condition with
the effective use of limited water for the sustainable crop production especially in low fertilization level.

Keywords: drought resistance, fertilization levels, NERICA, soil water content, stomatal conductance

Introduction

Global water shortages are getting worse and drought is the major constraint to the crop
production (Blum, 2009, Boyer, 2010, Serraj et al., 2011). Recently NERICA (New Rice for Africa)
th
was developed by a crossing between African rice (Oryza glaberrima Steud.) with Asian rice (Oryza
sativa L.) in West Africa, and is considered to be drought resistant, but it is not clarified enough
about the difference in reactions under dry condition. In this research, NERICA, Asian rice, African
rice and millets were cultivated in the field under drought condition with different fertilization levels to
compare dry matter production, stomatal and leaf characteristics and water absorbing
characteristics to confirm the characteristics of NERICA under drought condition.


Plant Materials and Cultivation
In this study two NERICA lines which showed superior drought resistant in our previous
reports (Fujii et.al, 2004, 2008) and their two parent cultivars were used. Cultivars WAB450-24-3-
P3-1-HB, WAB450-I-B-P-82-2-1, sativa parent: WAB56-104, glaberrima parent: CG14. Rice
cultivars of O. sativa L. (Koshihikari (japonica, lowland, Japan), Dular (indica, lowland-upland, India)
and IRAT13 (japonica, upland, Cote dIvoire)) and common millet (Panicum miliaceum L.) were also
used. Plants were seeded in paper pots on May 31, 2007 and seedlings were planted at upland
field in the vinyl house of Shizuoka University on June 21. Sides of vinyl house were kept open.
Irrigation was applied on June 21, 27 and July 10, and after that no irrigation was applied. Plots
were fertilized by compound fertilizer at the rate of 6 g/m
2
as nitrogen in standard fertilization plots
and 2 g/m
2
in low fertilization plots individually.

Measurements
Plants were sampled on June 25, July 31, September 13 and October 22 at the harvesting
time. After dividing into organs, dry weight was measured after desiccating in the drying oven.
Stomatal conductance was measured at the center of abaxial side of topmost three leaves by
dynamic diffusion porometer (AP4, Delta-T Devices Ltd., Cambridge, UK) on sunny days during the
daytime. Measurements were made on August 7, 13 and 20. Soil water contents at individual
depths were measured by TRIME-T3 tube access probe system (IMKO micromodultechnik,
Ettlingen, Germany) by TDR method. Measurements were made at intervals of 10cm depth on
August 6, 17, 30 and September 11.
Leaf thickness was measured by micrometer (No.193-111, Mitutoyo, Kawasaki, Japan) at
the middle length of topmost fully extended leaves avoiding midrib on August 10, 17, 22, 30 and
September 12. SPAD value was measured by SPAD meter (SPAD502, Konica Minolta, Tokyo,
Japan) on August 10, 17, 22, 30 and September 10. Both measurements were replicated 10 times
in each plot.


Top Dry Weight
In standard fertilization level under drought condition, top dry weight at harvest was high in
Dular, drought resistant cultivar in Asian rice (Figure1). Dry weight at harvest in low fertilization level
tended to be higher than in standard fertilization level. In low fertilization level one of NERICA
showed high dry weight. Dry weight in glaberrima parent of NERICA was high in both standard and
low fertilization levels, but proportion of dead leaf was high and heading was not observed.

th
Dry Weight at Harvest (Oct. 22)
0
200
400
600
800
1000
1200
1400
K
o
s
h
i
h
i
k
a
r
i
D
u
l
a
r
I
R
A
T
1
3
s
a
t
i
v
a

p
a
r
e
n
t
W
A
B
4
5
0
-
2
4
-
3
-
P
3
-
1
-
H
B
W
A
B
4
5
0
-
I
-
B
-
P
-
8
2
-
2
-
1
g
l
a
b
e
r
r
i
m
a

p
a
r
e
n
t
c
o
m
m
o
n

m
i
l
l
e
t
L

K
o
s
h
i
h
i
k
a
r
i
L

D
u
l
a
r
L

I
R
A
T
1
3
L

s
a
t
i
v
a

p
a
r
e
n
t
L

W
A
B
4
5
0
-
2
4
-
3
-
P
3
-
1
-
H
B
L

W
A
B
4
5
0
-
I
-
B
-
P
-
8
2
-
2
-
1
L

g
l
a
b
e
r
r
i
m
a

p
a
r
e
n
t
L

c
o
m
m
o
n

m
i
l
l
e
t
D
r
y

W
e
i
g
h
t

g
/
m
2
Dead Leaf
Stem
Leaf
Ear

Bars show standard errors.

Figure1. Top dry weight of individual organs at harvest, Oct. 22.

Stomatal Conductance
In standard fertilization level Dular showed highest stomatal conductance followed by
sativa parent of NERICA and one of NERICA (Figure 2). In low fertilization level sativa parent of
NERICA, Dular and one of NERICA showed high stomatal conductance and it tended to be higher
than in standard fertilization level. Glaberrima parent of NERICA showed low stomatal conductance
in both fertilization levels.
0
40
80
120
160
K
o
s
h
i
h
i
k
a
r
i
D
u
l
a
r
I
R
A
T
1
3
s
a
t
i
v
a

p
a
r
e
n
t
W
A
B
4
5
0
-
2
4
-
3
-
P
3
-
1
-
H
B
W
A
B
4
5
0
-
I
-
B
-
P
-
8
2
-
2
-
1
g
l
a
b
e
r
r
i
m
a

p
a
r
e
n
t
c
o
m
m
o
n

m
i
l
l
e
t
L

K
o
s
h
i
h
i
k
a
r
i
L

D
u
l
a
r
L

I
R
A
T
1
3
L

s
a
t
i
v
a

p
a
r
e
n
t
W
A
B
4
5
0
-
2
4
-
3
-
P
3
-
1
-
H
B
W
A
B
4
5
0
-
I
-
B
-
P
-
8
2
-
2
-
1
L

g
l
a
b
e
r
r
i
m
a

p
a
r
e
n
t
L

c
o
m
m
o
n

m
i
l
l
e
t S
t
o
m
a
t
a
l

C
o
n
d
u
c
t
a
n
c
e

m
m
o
l
/
m
2
/
s

Bars show standard errors

Figure 2. Average stomatal conductance from August 7 to 20.

Soil water content
Average soil water content at 0-60 cm depth before harvest in standard fertilization level
was low in Dular followed by glaberrima parent of NERICA. In low fertilization level soil water
content was maintained highest in one of NERICA. Soil water content at 0-20 cm depth in standard
fertilization level was low in glaberrima parent of NERICA (Figure 3). There was large cultivar
differences in soil water content at 40-60 cm depth and soil water decreased significantly in Dular in
standard fertilization level (Figure 4). On the contrary it was maintained highest in one of NERICA in
low fertilization level.

th
0-20cm depth on September 11
0
5
10
15
K
o
s
h
i
h
i
k
a
r
i
D
u
l
a
r
I
R
A
T
1
3
s
a
t
i
v
a

p
a
r
e
n
t
W
A
B
4
5
0
-
2
4
-
3
-
P
3
-
1
-
H
B
W
A
B
4
5
0
-
I
-
B
-
P
-
8
2
-
2
-
1
g
l
a
b
e
r
r
i
m
a

p
a
r
e
n
t
c
o
m
m
o
n

m
i
l
l
e
t
L

K
o
s
h
i
h
i
k
a
r
i
L

D
u
l
a
r
L

I
R
A
T
1
3
L

s
a
t
i
v
a

p
a
r
e
n
t
L

W
A
B
4
5
0
-
2
4
-
3
-
P
3
-
1
-
H
B
L

W
A
B
4
5
0
-
I
-
B
-
P
-
8
2
-
2
-
1
L

g
l
a
b
e
r
r
i
m
a

p
a
r
e
n
t
L

c
o
m
m
o
n

m
i
l
l
e
t
E
v
a
p
o
r
a
t
i
o
n

P
l
o
t
S
o
i
l

W
a
t
e
r

C
o
n
t
e
n
t

Figure 3. Soil water content at 0-20 cm depth on September 11.

0
10
20
30
40
K
o
s
h
i
h
i
k
a
r
i
D
u
l
a
r
I
R
A
T
1
3
s
a
t
i
v
a

p
a
r
e
n
t
W
A
B
4
5
0
-
2
4
-
3
-
P
3
-
1
-
H
B
W
A
B
4
5
0
-
I
-
B
-
P
-
8
2
-
2
-
1
g
l
a
b
e
r
r
i
m
a

p
a
r
e
n
t
c
o
m
m
o
n

m
i
l
l
e
t
L

K
o
s
h
i
h
i
k
a
r
i
L

D
u
l
a
r
L

I
R
A
T
1
3
L

s
a
t
i
v
a

p
a
r
e
n
t
L

W
A
B
4
5
0
-
2
4
-
3
-
P
3
-
1
-
H
B
L

W
A
B
4
5
0
-
I
-
B
-
P
-
8
2
-
2
-
1
L

g
l
a
b
e
r
r
i
m
a

p
a
r
e
n
t
L

c
o
m
m
o
n

m
i
l
l
e
t
E
v
a
p
o
r
a
t
i
o
n

P
l
o
t
S
o
i
l

W
a
t
e
r

C
o
n
t
e
n
t

(
g
/
c
m
3
,
%
)
40-60cm depth on September 11

Figure 4. Soil water content at 40-60cm depth on September 11.

Relationship between stomatal conductance and dry weight
There was a significant correlation (r=0.907
**
) between average stomatal conductance and
dry weight at harvest except glaberrima parent of NERICA (Figure 5). In low fertilization level
stomatal conductance and dry weight at harvest tended to be larger than in standard fertilization
level.
0
200
400
600
800
1000
1200
1400
0 20 40 60 80 100 120 140
Average Stomatal Coductance (mmol/m
2
/s)
D
r
y

W
e
i
g
t

a
t

H
a
r
v
e
s
t

(
g
/
m
2
)
Asian rice
NERICA
African rice
Common millet
L Asian rice
L NERICA
L African rice
L Common millet
Asian rice, NERICA
r=0.907**
African rice
Common millet

**: significant at 1%
Figure 5. Relationship between average stomatal conductance from August 7 to 20 and top dry weight at
harvest on Oct. 22.

th
Relationship between leaf thickness and dry weight
**
) between average leaf thickness and dry
weight at harvest except glaberrima parent of NERICA and cultivar with thick leaf tended to
maintain high dry matter production (Figure 6).

0
400
800
1200
1600
0.12 0.16 0.2 0.24
Average Leaf Thickness (mm)
D
r
y

W
e
i
g
t

a
t

H
a
r
v
e
s
t

(
g
/
m
2
)
Asian rice
NERICA
African rice
Common millet
L Asian rice
L NERICA
L African rice
L Common millet
Asian rice, NERICA
r=0.892**
African rice
Common millet


Figure 6. Relationship between average leaf thickness from August 10 to September 12 and top dry weight at
harvest on Oct. 22.

Relationship between leaf thickness and SPAD value
**
) between average leaf thickness and SPAD
value in rice (Figure 7). In one of NERICA leaf thickness and SPAD value were higher in low
fertilization level than in standard fertilization level. SPAD value tended to be low in Dular.

20
30
40
50
0.12 0.16 0.2 0.24
Average Leaf Thickness (mm)
A
v
e
r
a
g
e

S
P
A
D

V
a
l
u
e
Asian rice
NERICA
African rice
Common millet
L Asian rice
L NERICA
L African rice
L Common millet
rice
r=0.828**
Common millet

Figure 7. Relationship between average leaf thickness from August 10 to September 12 and average SPAD
value from August 10 to September 10.

Conclusions

Dry weight was high in Dular, but soil water content decreased especially in the standard
fertilization level. On the contrary dry weight was high in one of NERICA and soil water content was
maintained high especially in low fertilization level and at deep soil layer. High leaf thickness and
th
SPAD values seem to be effective to maintain dry matter production under limited water condition
with high water use efficiency. Condon et al. (2004) showed cultivar differences in water use
efficiency in wheat. In rice, NERICA seems to be appropriate for the cultivation under drought
condition with the effective use of limited water for the sustainable crop production especially in low
fertilization level.

Acknowledgements

We thank Emeritus Professor Horie and Professor Shiraiwa, Kyoto University, for kindly giving an
opportunity to use seeds of NERICA lines in this study.

References

Blum A. 2009. Effective use of water (EUW) and not water-use efficiency (WUE) is the target of crop yield
improvement under drought stress. Field Crops Res. 112:119-123.
Boyer JS. 2010. Drought decision-making. J. Exp. Bot. 61(13): 3493-3497.
Condon AG, RA Richards, GJ Rebetzke and GD Farquhar. 2004. Breeding for high water-use efficiency. J. Exp.
Bot. 55: 2447-2460.
Fujii M, Andoh C and Ishihara S. 2004. Drought resistance of NERICA (New Rice for Africa) compared with
Oryza sativa L. and millet evaluated by stomatal conductance and soil water content In Fischer T et al.
New directions for a diverse planet: Proceedings for the 4th International Crop Science Congress,
Brisbane, Australia, 26 September - 1 October 2004. www.cropscience.org.au/icsc2004 5pages.
Fujii M, Y Miyamoto and S Ishihara. 2008. Studies on drought resistance of Asian rice (Oryza sativa L.) and
NERICA -Water use in the field- In Abstracts of the 5
th
International Crop Science Congress & Exhibition,
April 13-18, 2008, Jeju, Korea: 209.
Serraj R, KL McNally, I Slamet-Loedin, A Kohli, SM Haefele, G Atlin and A Kumar. 2011. Drought resistance
improvement and resource management strategy. Plant Prod. Sci. 14(1)

th
Social Experiment of Volumetric Irrigation Fee Scheme:
Case of Gravity Irrigation System in Bohol, the Philippines

Shigeki Yokoyama
a*
, Kei Kajisa
b
, Tatsuro Miyazaki
c

a
Japan International ResearchCenter for Agricultural Sceinces, Tsukuba, Japan
b
International Rice Research Institute, Los Banos, the Philippines
c
Tsukuba University, Tsukuba, Japan
* Corresponding author: Japan International ResearchCenter for Agricultural Sceinces,
Ohwashi 1-1, Tsukuba, 305-8686, Japan.
Tel.: +81 29 838 6343; fax: +81 29 838 6342.
[email protected]

Abstract

Increasing in water productivity in rice is crucial as irrigated rice production consume a substantial part of the
total worlds fresh water. To promote the adoption of water saving technologies, farmers are provided with a
tangible incentive to save water is necessary. The social experiment survey of volumetric pricing had been
conducted in Bohol, the Philippines, where double rice cropping has been started since 2008 under gravity
irrigation. The preliminary results showed that both economic incentive and technical training promoted the
efficient water use.

Keywords: social experiment, volumetric pricing, AWD, gravity irrigation, the Philippines

Introduction

The current scheme of irrigation fee, in most of Asia, is charged according to the area
irrigated. This scheme may induce overuse of irrigation water as the payment amount is fixed
regardless of the actual water use. Area basis charge scheme has long been practiced due to
technical difficulty of measuring water intake at farm level, for gravity irrigation system in particular.
Fresh water has become increasingly scarce resource worldwide due to increasing in demand of
urban and industrial use. Global warming and climate change may worsen this situation.
Considering that irrigated rice production consume a substantial part of the total worlds
fresh water use, increasing in water productivity in rice is crucial (Shivakoti et al 2005). To promote
the adoption of water saving technologies, providing farmers with a tangible incentive to save water
is necessary. Charging irrigation fee according to the volume of actual water use is such an
incentive. The social experiment survey of volumetric pricing had been conducted in Bohol, the
Philippines, where double rice cropping has been started since 2008 under gravity irrigation.
Research questions were: 1) Whether volumetric incentive effectively induces water saving efforts
of water users group, and 2) Whether training of water saving technology (Alternate Wetting and
Drying, AWD) contributes efficient water use.


Bayongan Dam System of Bohol Integrated Irrigation System, Stage II (BIS-II), was
selected as the study site (Map) (Figure 1). The system was constructed with the financial and
technical support of JICA (Japan International Cooperation Agency). The system started operation
in May 2008 covering 4,000 ha (designed area).The main canal of 6,662 m and 15 laterals, Lateral-
A to O, are fully lined, and each TSA (Turnout Service Area, unit of water users) is equipped with
th
spindle gate, by which farmers can control water intake by themselves, and a level gauge by which
the volume of water is measured by the third party (Nippon Koei et al. 2007).
The experiment design was as follows. The volume of water intake was estimated based
on the gauge reading three times a day (morning, noon and afternoon) at head gate of each TSA.
Irrigation fee was firstly collected by area basis as usual, then to be paid back to TSA according to
the percentage of saved water based on the required water volume for conventional continuous
flooding practice.
Randomized field experiment was applied to 67 TSAs of upper portion of the system
among total 147 TSAs. The data collections were conducted for five crop seasons from November
2008 to May 2011. No intervention was applied in the season 0 for all samples as the base line.
Volumetric incentives had been applied to the half of TSAs randomly selected for four seasons from
the season 1 to the season 4. Technical training of AWD was provided to the half of experimental
TSAs and the half of control TSAs before the season 3 (May-Sep 2010). These two interventions
resulted in the four groups (Table 1).

Figure 1. Map of the Philippines.

Table 1. Number of sample TSAs by treatment and season

Season 0
Nov08-Mar09
1
May-Sep09
2
Dec09-Apr10
3
Jun-Nov10
4
Dec10- May11
Treatment
67
34 34
16 16 CC
18 18 CA
33 33
20 20 VC
13 13 VA
CC: No intervention
CA: AWD training only
VC: Volumetric only
VA: Volumetric and AWD training

Study Site
(Bohol Island)
th

In this analysis only the data of the season 0 to 3 were used, as the data of season 4 was
still being processed. Profile of the sample TSAs is presented in Table 2. The average size of TSA
was around 15 ha of irrigated paddy field with 25 members of farmers. Double rice cropping was
practiced in irrigated paddy, while rice-upland crop in rainfed paddy and cassava in upland were
common cropping systems. As the designed irrigation area was larger than the actual one, land
leveling was still in process and irrigated area was gradually expanding. Main Farm Ditch (MFD)
was the soil canal draws water from a lateral into TSA area. National Irrigation Administration (NIA)
was responsible to design and construct MFD, while after completion its maintenance was assigned
to each TSA. Efficient water use and equity distribution among the members were highly dependent
on operation and maintenance of MFD. Almost all of the TSAs organize a regular monthly meeting
and collective maintenance work as members obligation. In average, water intake reduced by 30%
from Season 0 as baseline to Season 3, the third session of the experiment. Though other factors
affecting water intake such as rainfall should be carefully took into account, the experiment seems
successful as a whole.

Table 2. Profile of sample TSAs

n=67 Average STDV
Number of members/TSA

Season 0 (Nov08-Mar09) 24.7 14.4
Length of Main Farm Ditch (m)

Season 0 (Nov08-Mar09) 650.5 495.2
Area irrigated (ha)

Season 0 (Nov08-Mar09) 14.36 9.32
Season 3 (Jun10-Nov10) 16.44 9.02
Water intake (m
3
/ha)

Season 0 (Nov08-Mar09) 10,600 5,493
Season 3 (Jun10-Nov10) 7,308 4,964
Source: TSA interview survey, 2009.

Table 3. Rice yield under rainfed and irrigation by Lateral

Lateral
Rainfed (2007)

Irrigated (2009)
Irrg/Rain
n Average (t/ha) STDV

n Average (t/ha) STDV
A 28 2.39 0.67

84 2.79 1.43 1.17
B 5 2.46 0.59

12 2.22 0.86 0.90
C NA NA NA

10 2.62 0.72 NA
D 11 2.68 0.83

29 2.92 1.59 1.09
E 5 2.04 0.55

14 2.87 1.6 1.41
F 13 2.02 1.14

33 2.42 1.39 1.20
G 5 1.86 0.9

14 2.67 1.45 1.44
Note: Lateral, A to G, aligns from up to down along the main canal.

Before evaluating the impacts of the experiment in detail, the effects of irrigation
construction were briefly examined. The rice yield increased by 20 to 40% after irrigation, with some
exception (Table 3). It should be noted that the effect was more obvious in down portion, suggesting
th
irrigation contributed to not only production increase as a whole but also to mitigation of spatial
disequilibrium.

Change in Locational Water Distribution
The distribution of water intake by TSA in Season 0 and 3 are shown in Figure 2. As
expected, there was a tendency that TSAs in upper portion used more water than those in lower
portion both at lateral level and within a lateral. This finding was consistent with the frequently cited
Upstream vs Downstream problem. Taking the advantage of position in the system, farmers in
upstream likely to take water excessively under the condition of area basis water fee. This caused
water shortage in the downstream, often resulting in conflict between the up- and downstream
farmers. It is worth to point out that additional water use did not necessary resulted in higher yield
(Table 3). This suggested that saving water in upper portion could contribute to increase in total rice
production of the system level, provided saved water is to be effectively distributed down portion
which suffers insufficient and unstable water supply.
Comparing the two seasons, a down ward slope from right to left became slightly flattened
after experiencing three experiments. The upper portion (Lateral A-D) saved more water than the
lower E-F, suggesting saved water was transferred to down portion (Lateral G and after), resulted in
more equitable water distribution in the system-wide.

y = -248.54x + 14953
R = 0.2259
0
5000
10000
15000
20000
25000
30000
A
-
1
A
-
3
A
-
6
A
-
7
A
-
9
A
-
1
0
A
-
1
1
B
-
3
B
-
4
C
-
1
C
-
2
C
-
4
D
-
1
D
-
2
D
-
3
D
-
4
D
-
6
D
-
7
D
-
8
D
-
9
E
-
1
E
-
2
E
-
3
E
-
4
E
-
5
F
-
1
F
-
4
F
-
5
F
-
6
F
-
7
F
-
8
F
-
9
F
-
1
0
F
-
1
1
F
-
1
3

y = -201.85x + 9260.2
R = 0.2189
0
5000
10000
15000
20000
25000
30000
A
-
1
A
-
3
A
-
6
A
-
7
A
-
9
A
-
1
0
A
-
1
1
B
-
3
B
-
4
C
-
1
C
-
2
C
-
4
D
-
1
D
-
2
D
-
3
D
-
4
D
-
6
D
-
7
D
-
8
D
-
9
E
-
1
E
-
2
E
-
3
E
-
4
E
-
5
F
-
1
F
-
4
F
-
5
F
-
6
F
-
7
F
-
8
F
-
9
F
-
1
0
F
-
1
1
F
-
1
3

Figure 2. Spatial distribution of water intake by TSA.
(m
3
/ha)
Season 0 (Nov08-Mar09)
Season 3 (Jun10-Nov10)
TSA
TSA
th
6000
7000
8000
9000
10000
11000
0 1 2 3
CC
CA
VC
VA
Effects of Experimental Intervention
For further examining farmers response to experimental interventions, changes in water
intake by experimental group were compared. Average of water intake by experimental group is
presented in Figure 3. Corresponding to the difference of experimental interventions, CC and CA
were treated as one group, same as VC and VA, from Season 0 to 2. As the samples were selected
randomly, water intakes of the two groups were mostly identical at the baseline (Season 0). The
volume has been consistently declined including the control group (CC). The factors affecting
overall water intake other than the experiment are rainfall, amount of water release from the dam,
NIAs promotion of water saving technology. To evaluate the experiment effects separately from
these factors, deviation of experimental groups from the control group should be focused. Economic
incentive for water saving was effective, and efficacy of water saving efforts seem to be intensified
as time goes. It seems that once farmers are convinced of no adverse effects on crop production
(Season 1), they continue water saving efforts and learned effective ways by themselves (Season
2-3).
Providing technical training also showed its effectiveness, as the group of AWD training
only (CA) substantially declined their water use compared with the control group (Season 3). There
was anecdotal evidence from farmer interview, indicating ADW or intermittent irrigation may
enhance yield by increased number of tillers and mitigating damage of golden apple snail. During
the experiment period, farmers had chance to learn these information from their neighbors. Part of
the sharp decline from Season 2 to 3 might be explained by this spillover effect. In addition, farmers
had also chance to attend trainings by NIA and other institutions such as extension offices and
NGOs. The synergy effect of economic incentive and training was not obvious. The performance of
the group of volumetric and training (VA) is not so striking compared with the group of volumetric
only (VC) and training only (CA) (Season 3).

Experiment Season

CC (n=16): No intervention; CA (n=18): AWD training only
VC (n=20): Volumetric only; VA (n=13): Volumetric and AWD training

Figure 3. Change in water intake by experimental group.

Conclusions

The preliminary results of social experiment for volumetric water pricing clearly show 1)
farmers well respond to economic incentive to save irrigation water use, 2) technical training was
also effective to reduce water intake independently of economic incentive, 3) saved water was
efficiently redistributed to down portion, enhancing system-wide equity. In this preliminary study
social factors, which are highly expected to influence collective actions like irrigation management,
(m
3
/ha)
th
were not considered. Reduced water may entail the risk of yield loss, while technical training and
collective actions for water saving may contribute to yield increase and stabilization. These were the
remaining issues for further analyses.

References

Nippon Koei Co Ltd, PKII Engineers, Integrated Philconsult, Inc and Sustainable Development Solutions, Inc.
2007. Bohol Irrigation Project Phase II, Operation and Maintenance Manual for Bayongan & Capayas
System Vol. 3.
Shivakoti GP, DL Vermillion, WF Lam, E Ostrom, U Pradhan and R Yonder eds. 2005. Asian irrigation in
transition: Responding to challenges. Sage Publication, New Delhi. pp 528.

th
Ultraviolet-induced Fluorescence of Rice Leaf as Influenced
by Nitrogen Application and Cultivars

Mikio Sekinuma
a,*
, Takehiro Natori
b
, Futoshi Sasaki
a
, Futoshi Kato
b
, Naoto Inoue
a,b

a
Interdisciplinary Graduate school of Science and technorogy, Shinshu University, Japan
b
Faculty of Agriculture, Shinshu University, Japan
* Corresponding author: Shinshu University, 8304 Minamiminowa, 399-4598 Nagano, Japan.
Tel.: +81 265 77 1409; fax: +81 265 77 1409.
[email protected]
<

Abstract

New measurement system of ultraviolet-induced fluorescence was developed for detecting the secondary
metabolic materials and chlorophyll fluorescence in order to evaluate the photosynthetic activity of crops. In this
study, 4 rice cultivars; Koshihikari, IR72, Banten (traditional javanica variety), and CH86 (traditional indica
variety), were grown in pots and nitrogen fertilizers were added in 5 different levels. Fluorescence of leaves was
measured before and after the heading stage. Leaf blades were excited by light of 370 nm wavelength, which
was derived by passing light from xenon lamp through a band-pass filter. The results showed that the
fluorescence peaks were located in the region of 400-650 nm, 685 nm and 740 nm, and the spectrum patterns
varied among cultivars and different nitrogen levels. Fluorescence intensity (400-650 nm wavelength) observed
under high nitrogen condition were relatively low as compared with observed under low nitrogen conditions.
These results indicated that the fluorescence pattern of the leaf blade was affected from plant growth and
nitrogen level of soil. Our findings show that spectrum analysis of ultraviolet-induced fluorescence is useful for
evaluation of rice plant nutrition.

Keywords: ultraviolet-induced fluorescence, nondestructive, rice

Introduction

Development of plant nutrition diagnosis systems is required for sustainable food
production in order to conserve resources. Diagnosis of crop is able to provide good information
about plant conditions, especially the nutrition status of a plant. Moderate amounts of fertilization
make it possible to conserve resource, and cost and to half nutrient enrichment of the soil.
In rice cultivation, increase of yield was established by restricting nitrogen supply in the
middle of the growth stage (Matsushima et al., 1964; Matsushima et al., 1966), as excess nitrogen
caused lodging. Nitrogen restriction was determined with basis on leaf color (Matsushima et al.,
1970; Matsuzaki et al., 1974). This cultivation method was termed the V-shaped rice cultivation.
Using leaf color to enable diagnosis is delaminated with information only of the leaf surface.
However, recent studies have attempted express to express the condition of a plant through
analysis of internal leaf conditions; many methods have succeeded more easily with indirect
estimation. Direct detection will be expected to estimate photosynthetic ability and function in the
future of diagnosis.
A useful diagnosis method is light detection by chlorophyll fluorescence. Fluorescence
detection has been used as a nondestructive, noncontact, and continuous detection method to
evaluate photosynthetic ability (Zoran et al., 1999). Chlorophyll concentration and water stress are
monitored by calculating the ratio of chlorophyll fluorescence (Saito, 2005).
The choice of an excitation light source is important in chlorophyll fluorescence because it
determines the fluorescence information that can be obtained. Visible (blue) excitation for plants
emits both red (RF, 630700 nm) and far-red fluorescence (FRF, 700800 nm). Ultraviolet (UV)
excitation emits RF, FRF, and blue-green fluorescence (BGF, 400630 nm). The BGF spectrum
th
includes information on leaf materials and structure, and this information reveals plant cultivation
conditions that are related to chlorophyll a information.
In this study, we developed a new UV-induced fluorescence measurement system to
detect the fluorescence of secondary metabolic materials and of chlorophyll in order to evaluate the
photosynthetic activity of crops. To achieve this purpose, we investigated whether our system was
able to distinguish rice cultivar and nitrogen fertilizer levels.


Plant material
Four rice cultivars, Koshihikari (Japonica), IR72, Banten (traditional javanica variety), and
CH86 (traditional indica variety), were grown in pots and nitrogen fertilizers were added in 5
different amounts (Table 1). The rice was grown in the Shinshu University greenhouse in Nagano
Prefecture (3551N, 13756E, 740 m above sea level). Measurement of leaf fluorescence was
carried out twice, before and after the heading stage, in 2010. The fluorescence of the cut leaves
was measured after dark adaption for 30 min at 25C. Room temperature was maintained at 25C
with air conditioning.

Table 1. Plant material

Cultivar Ecotype Plant type Notes
Koshihikari Japonica Standard Japanese commercial var.
IR72 Indica Multi tillering
BANTEN Javanica Large panicle
CH86 Indica Grassy Yellow leaf

Fluorescence measurements
Figure. 1 illustrates the new fluorescence measurement system (FMS) for detection of the
fluorescence spectrum. In this system, leaf blades were excited by a 370 nm-wavelength light
derived by passing light from a xenon lamp (LAX101, Asahi Spectra Co., Ltd., Japan) through a
band-pass filter at 370 nm (XBPA370, Asahi Spectra Co., Ltd., Japan). UV light was directed to the
target leaf through a quartz fiber. The band-pass filter had a center wavelength of 370 nm with a 10
nm half-bandwidth. The detector unit was a Photonic Multichannel Analyzer (PMA-11, Hamamatsu
Photonics, Japan). A long-pass filter (XUL0400, Asahi Spectra Co., Ltd. Japan) was positioned in
front of the detection fiber and the reflection of light below a 400 nm wavelength was ensured. The
detected fluorescence wavelength was 400850 nm. The distance between the edge of the fiber
and the leaf sample was adjusted to approximately 5 mm. The PMA was operated in 50 msec
durations for each leaf area (point) and this was repeated 1000 times in the same area to determine
fluorescence excitation. Each leaf sample consisted of 5 areas (point). The acquisition spectra were
determined as the highest peak of the spectrum that had a maximum intensity at 680 nm and 740
nm in the 1000 runs. The acquisition spectra were identical to the mean spectra of peak timing in
the Kautsky curve (Govindjee, 1995).
th
Leaf blade
Long-
pass
filter
Exciting unit
(Xenon light)
Detecting
unit
(Photonic
Multichannel
Analyzer)
Personal
computer
Band-
pass
filter
Fluorescence
(360nm<380nm)
(400nm<)
Coaxial
fiver
Date

Figure 1. Schematic diagram of fluorescence measurement system. Detected bandwidth of spectrum had
wavelengths of 400850 nm.


Figure 2 indicates the fluorescence patterns of leaf blades at various nitrogen levels. The
fluorescence peaks were in the region of 400650 nm, 685 nm, and 740 nm, and the spectrum
patterns varied with the different nitrogen levels. The intensity of BGF observed under high-nitrogen
conditions was low compared with BGF intensity observed under low-nitrogen conditions.

0
100
200
300
400
500
600
400 500 600 700 800 900
F
l
u
o
r
e
s
c
e
n
e

i
n
t
e
n
s
i
t
y

(
C
o
u
n
t
s
)
Wavelength (nm)
(A) Koshihikari
0Ng/m2
5Ng/m2
20Ng/m2

0
100
200
300
400
500
600
400 500 600 700 800 900
F
l
u
o
r
e
s
c
e
n
e

i
n
t
e
n
s
i
t
y

(
C
o
u
n
t
s
)
Wavelength (nm)
(B) IR72
0Ng/m2
5Ng/m2
20Ng/m2
0 Ng/m
2
5 Ng/m
2
20 Ng/m
2

0
100
200
300
400
500
600
400 500 600 700 800 900
F
l
u
o
r
e
s
c
e
n
e

i
n
t
e
n
s
i
t
y

(
C
o
u
n
t
s
)
Wavelength (nm)
(C) Banten 0Ng/m2
5Ng/m2
20Ng/m2
0 Ng/m
2
5 Ng/m
2
20 Ng/m
2

0
100
200
300
400
500
600
400 500 600 700 800 900
F
l
u
o
r
e
s
c
e
n
e

i
n
t
e
n
s
i
t
y

(
C
o
u
n
t
s
)
Wavelength (nm)
(D) CH86
0Ng/m2
5Ng/m2
20Ng/m2
0 Ng/m
2
5 Ng/m
2
20 Ng/m
2

(A) Koshihikari, (B) IR72, (C) BANTEN, (D) CH86.

Figure 2. Fluorescence spectra of rice leaf. The spectra by excitation at 370 nm were measured at the leaf apex
prior to the heading stage.

th
0
100
200
300
400
500
600
400 500 600 700 800 900
F
l
u
o
r
e
s
c
e
n
e

i
n
t
e
n
s
i
t
y

(
C
o
u
n
t
s
)
Wavelength (nm)
Koshihikari
IR72
BANTEN
CH86
Figure 3 illustrates the fluorescence spectrum of each cultivar. Fluorescence intensity
varied with each cultivar, and high BGF intensity was obtained from the Koshihikari spectrum.
These results might describe the fluorescence information containing the condition of plant
metabolic material affected by nitrogen levels. The effect of nitrogen treatment was related to BGF
intensity. BGF is caused by excitation of ferulic acid derivatives, other phenylpropanoids, and
NAD(P)H; RF and FRF are caused by excitation of chlorophyll a (Cerovic et al., 1999). BGF
enables monitoring of the influence of nitrogen on the degree of growth. We believe that this system
can function as a nitrogen level monitor at the same growth stages in rice.

Figure 3. Fluorescence spectra for the cultivars. The spectra by excitation at 370 nm were measured at the leaf
apex prior to the heading stage. All cultivars were grown at 5 Ng/ m
2
.

The fluorescence spectrum of each cultivar demonstrated different patterns. However, we
also need to consider leaf structure, rate of development, and the response to nutrients. In
fluorescence detection, it has been suggested that a balance of FRF and BGF enables estimation
of wheat lamina growth (Meyer, 2003). In this study, the balance of FRF and BGF may have
enabled monitoring of the degree of growth for the cultivars. This result suggests that the detection
for cultivars requires further testing and analysis in combination with their growth rates and
conditions.
In conclusion, the differences in these results indicate that soil nitrogen levels and different
cultivars influence the fluorescence patterns of leaf blades. Our findings show that spectrum
analysis of UV-induced fluorescence is useful for evaluation of rice plant nutrition. In the future, UV
laser-induced fluorescence methods will be developed if a new diagnosis system becomes
necessary.

References

Govindje E. 1995. Sixty-Three Years Since Kautsky: Chlorophyll a Fluorescence. AUST. J. PLANT PHYSIOL.
22: 131160.
Matsushima S, Matsuzaki A and Tomita T.1964. Analysis of Yield-Determining Process and Its Application to
Yield-Prediction and Culture Improvoment of Lowland Rice : . Studies on the principles for
maximizing yield and their demonstration (1). JPN. J. CROP. SCI. 32: 48-52.
Matsushima S, Wada G and Matsuzaki A.1966. Analysis of Yield-Determining Process and Its Application to
Yield-Prediction and Culture Improvoment of Lowland Rice : . Studies on the principles for
maximizing yield and their demonstration (3). JPN. J. CROP. SCI. 34: 321-328.
Matsushima S, Matsuzaki A and Tomita T.1970. Analysis of Yield-Determining Process and Its Application to
Yield-Prediction and Culture Improvoment of Lowland Rice: . On a method for expressing the leaf-
colour of rice plants under field conditions (1). JPN. J. CROP. SCI. 39: 231-236.
th
Matsuzaki A, Matsushima S, and Tomita T.1974. Analysis of Yield-Determining Process and Its Application to
Yield-Prediction and Culture Improvoment of Lowland Rice : . Effects of the nitrogen restriction on
the grain yield juded from the frowth amount, the leaf color ant the percentage of stained length of leaf
sheath. JPN.J.CROP. SCI. 43: 167-173.
Meyer,S. A. Cartelat, I. Moya and Z. G. Cerovic. 2003. UV-induced blue-green and far-red fluorescence along
wheat leaves: a potential signature of leaf ageing. J. Exp. Bot. 54 (383): 757-769.
Saito Y, Matsubara T, Kobayashi F, kawahara T, and Nomura A. 2005. Laser-induced fluorescence
spectroscopy for in-vivo monitoring of plant activities. The 7thFruit, Nut and Vegetable Production
Engineering Symposium: 699-708
Zoran G. Cerovica, Guy Samsonb, Fermn Moralesc, Nicolas Tremblayd and Ismal Moyaa. 1999. Ultraviolet-
induced fluorescence for plant monitoring: present state and prospects. AGRONOMIE. 19 (7):543 578.

th
Locus for Malate Secretion in Rice Chromosome 3

Miftahudin
1
*, Irfan Martiansyah
1
, Dewi Indriyani Roslim
2
, Tatik Chikmawati
1

1
Department of Biology, Faculty of Mathematics and Natural Sciences, Bogor Agricultural University, Kampus
IPB Darmaga, Bogor-Indonesia
2
Department of Biology, Faculty of Mathematics and Natural Sciences, Universiy of Riau Pekanbaru, Riau
*Corresponding author: [email protected]

Abstract

Aluminum (Al) toxicity is a major limiting factor of rice production in acid soil. One of the tolerance mechanisms
of plant to Al stress is the secretion of malate from plant root. The objective of this research is to identifiy
quantitative triat loci (QTL) in chromosome 3 that controls malate secretion from rice root during the period of Al
stress. The research was conducted in laboratory and green house. An F2 population derived from the cross
between rice genotype Hawara Bunar and cultivar IR64 was used in this experiment. Analysis malate secretion
was carried out based on enzymatic method. Rice simple sequence repeats from chromosome 3 were as
moelcular marker. The mapping and QTL anaysis was performed using Mapmaker 3 and Mapmaker/QTL. The
result showed that the malate secretion trait was normally distributed in the rice F2 population indicating that the
trait is polygenic trait. A QTL for malate secretion was identified in the short arm of rice chromosome 3 located in
between markers RM545 and RM517.

Keywords: Aluminum stress, Chromosome 3, Rice, QTL

Introduction

In general, aluminum tolerance in plant is genetically controlled, and the diversity of this
trait can be found inter and intra plant species, including the member of Gramineae (Aniol and
Gustafson 1990). Aluminum tolerance mechanism in plant can be divided into two models (Kochian
1995, Matsumoto 2000). First, internal detoxification mechanism, which is the mechanism of plant
cells that are able to detoxify Al in the cell through organic acid chelation (Ma et 1998), vacuolar
accumulation, protein detoxification, or reactive oxigen species reduction in the root cells (Ezaki et
al 2000). Internal detoxification mechanism can also be achieved through activation of calmodulin-
independent NAD
+
kinase (Aniol, 1991).
In the second model, Al is excluded from root tip cells through excluding Al accors plasma
membrane, increasing rhizosfeer pH, producing exudate or secreting organic acid (Taylor 1991,
Kochian 1995). Among those external mechanisms, organic acid secretion from root cells, such
malate, citrate and oxalate, has been the most accepted mechanism. Organic acid secretion has
important role in Al tolerance mechanism in wheat, rye and maize (Ryan et al 1995, Li et al 2002,
Pellet et al 1995), however the similar role has not been elucidated in rice.
Several researchers have shown that organic acid secretion closely related to Al tolerance
mechanis. However, the main factor that controlled organic acid secretion from root cells during Al
stress still unclear. The recent finding showed that over expression of malate transporter gene that
isolate from wheat could increase Al tolerance in transgenic tobacco, but the gene could not
increase Al tolerance in rice (Sasaki et al 2004).
This paper reported our research in identifying locus for malate secretion trait in rice using
an F2 population derived from a cross between an Indonesian local rice genotype that tolerant to Al
and a rice variety IR64 that sensitive to Al. It is expected that the locus can be used to isolate the
gene controlling malate secretion in rice.

th
Materials and Method

Plant Materials
Rice genotype Hawara Bunar (Al-tolerant parent) and cultivar IR64 (Al-sensitive parent),
F1 plants and F2 population derived from a cross between Hawara Bunar and IR64 were used in
this research.

Nutrient culture technique for alumininum stress treatment
A simple hydrophonic technique was used to grow rice seedlings. Seeds were sterilized
and soak in destilate water for 24 hours, and followed by germination for 48 hours. The seedlings
with homogenous root length were put in sterofoamfloated on sterile minimal nutrient solution
(Miftahudin et al. 2004) at pH 4.0 in 15 ml tube. A 15 ppm of Al in the form of AlCl
3
.6H
2
O was
adminitered fro 24 hours. The seedlings were grown at room temperature in growth chamber with
12 hours light photoperiod.

Determination of malate secretion
Malate secretion was determined from F1 plants, 400 individual F2 population and both
parents. Determination of malate secretion followed procedure as described by Delhaize et al.
(1993). A 1.35 ml nutrient solution was sampled from each tube and was added with 1.5 ml buffer
solution (0.4 M hydrazine and 0.5 M glycine, pH 9) and 0.1 ml 40 mM NAD. The reaction mixtures
were thenincubated at room temperaturefor 30-60 min. The absorbance of the mixture was
measured using spectrophotometer at =340 nm (absorbance 1). The mixture was then added with
5 L Malate Dehidrogenase (5 mg/mL, Sigma, USA), and the absorbance 2 was then
measured.The difference between absorbance 1 and 2 indicated the amount of NADH produced
and was used to calculate malate content of the solution as the following equation:
V x M
C = --------------------------------- x A
x d x v x 1000

Notes: C = Malate concentration (mg/l)
V = Volume Total (ml)
v = Sample Volume (ml)
M = Molecular Weight of Malate (g/mol)
d = Cuvette width (cm)
= Absorption coefficientof NADH at 340 nm = 6.3 (l/mmol.cm)
A = the difference between absorbance 1 dan 2

Moelcular marker analysis
The polymorphic SSR markers from rice chromosome 3 were applied to 300 individuals F2
population. The primers from those markers were used to amplify DNA. A 50 ul PCR reaction
mixture consist of100 ng DNA, 100 mM Tris-Cl pH 8.0, 50 mM KCl, 2 mM MgCl
2
, 0.2 mM dNTPs,
0.3-0.5 uM tiap primer, and 1 U Taq DNA polimerase (NEB, USA) was made for each individual
plant. PCR process were performed using thermocycler with the following condition: 1 cycle of
94
o
C for 5 minutes followed by temperature cycles of94
o
C (35 second), 55
o
C (35 second), and 72
o
C
(1 minutes, 45 second) for 35 cycles and finally one cycle of 72
o
C for 10 minutes . PCR products
were analyzed using 2.5 - 3.0% superfine agarose gel electrophoresis in 0.5 x TBE (Tris-Borate-
EDTA) buffer.

th
Genetic mapping and QTL identification
Segregation analysis of molecular marker in the F2 population was performed using Chi
Squaretest pada o = 0.05. Genetic linkage and QTL analyses usedMAPMAKERS/EXP ver 3.0
andMAPMAKERS/QTL ver 1.1, respectively.


Malate secretion in parent plants under Al stress
Malate secretion was analyzed from nutrient culture media that has bee used for growing
F1, F2 and both parent seedling under 72 hours Al stress. The result showed that the malate
secretion was higher when the seedlings were Al stressed and the secretion increse as the period
of stress increase (Figure 1 and 2). The Al stress at thelevel of 15 ppm could differentiate malate
secretion level from both parents. In rice cv IR64, although malate secretion increase as the
increase of stress period, there was no significant difference between malate scretion at 0 and 15
ppm of Al stress along the 72 hour period of stress. Conversely, there wassignificant difference of
malate secretion along the 72 hours stress period between 0 and 15 ppm Al stressin Hawara
Bunar.The significant increase of malate secretion occurred when the seedlings were Al-stressed at
15 ppm at 72 hours. Therefore, the Al stress level of 15 ppm for 72 hour stress duration was used
for phenotyping the F2 population. The result also showed that the average malate secretion from
IR64, Hawara Buanr, F1 and F2 plants were 2.2, 3.8, 3.1 and 4.1 ppm, respectively.

Figure 1. Malate secretion from, rice root cv IR64 (a) and Hawara Bunar (b) along the 72 hour period of Al
stress.

a
b
th
Distribution of Malate Secretion in F2 Population
Analysis of malate secretion in 400 individual F2 population showed normal distribution
(Figure 2), which indicated that malate secretion character was multigenic controlled. It can be
seen from the Figure 2 that the distribution curve rather skewed to the right and the secretion class
falled to higher value than that both parents. This is suggested transgresive segregation
phenomenon in this population. The average malate secretion of F2 population was also higher
than that of Hawara Bunar.
When the malate secretion was grouped into two class of secretion based on the range of
each parent malate secretion, malate scretion in F2 population followed monogenic inharitance.
For individual F2 that secreted malate < 3 ppm, it was grouped into Al-sensitive plants, otherwise
the plants were grouped into Al-tolerant plants. The Chi square test showed that the segregation fit
to 3:1 ratio for Al-tolerant to Al-sensitive plants (Table1).

Figure 2. Distribution of malate secretion among individual F2 population.

Table 1. Chi square test for monogenic inharitance pattern of malate secretion in F2 population

Malate Secretion Class
(ppm)
Number of Observed
Plants
Number of
Expected Plants
(3:1)
Chi test
< 3.0 79 91
0.15

3.0 285 273

Locus for malate secretion in rice chromosome 3

Analysis of genetic factor controlling malate secretion trait in rice was performed into two
approaches. First, malate secretion trait was treated as polygenic trait based on the normal
distribution of malate secretion in the F2 population, and second, malate secretion trait was treated
as monogenic trait. The result showed that among the three chromosome that habe been
analyzed, which were chromosome 1, 2 and 3, the locus for malate secretion trait was only possibly
found om chromosome 3. QTL analysis based on poygenic trait indicated the presence of the QTL
in the short arm of chromosome 3 in the region between markers RM%$% and RM517. However,
the LOD score in that region maximum only 0.98, which was not enough to conclude that the QTL
present in that region.
When analysis was performed based on monogenic trait, it was found that a locus for
malate secretion trait present in the region with LOD 3.02. Genetic map of the rice chromosome 3
that harbored the locus for malate secretion trait contained five markers i.e. RM569, RM545,
RM517, RM251, and RM232 with the total distance 131.8 cM (Figure 3). The locus for malate
secretion trait was located in between marker RM545 and RM517 with the exact position at 4 cM
th
from RM517 toward RM545. The result of this research was similar to Nguyen et al (2001) who
found QTL position for Al tolerance loci in the short arm of rice chromosome 3, but the position is
rather shifted to other region of the short arm. This difference was due to the different rice
background used in both experiments.

Figure 3. Genetic map of malate secretion locus in rice chromosome 3.

Conclussion

Rice secreted malate during the period of aluminum stress. Al tolerant rice genotype
secreted malate more than that of Al-sensitive rice genotype. The secretion increased as the
duration of stress increase. There was a locus controlling malate secretion located in the short arm
of rice chromosome 3.

Acknowledgement

This research is supported by Basic Research Insentive Grant from Indonesian Ministry of Research
and Technology Year 2009 granted to Dr. Miftahudin.

References

Aniol A (1991) Genetics of acid tolerant plant. In Wright RJ, Baligar VC, Murrmann RP (eds) Plant-Soil
Interactions at Low pH. Kluwer Acad Publ, Dordrecht, pp.1007-10017
Aniol A, Gustafson JP (1990) Genetics of aluminum tolerance in agronomic plants. In Shaw AJ (ed) Heavy
Metal Tolerance in Plants: Evolutionary Aspects. CRC Press, Boca Raton, Florida, pp.255-267
Delhaize E, Ryan PR, Randall PJ (1993b) Aluminum tolerance in wheat (Triticum aestivum L.). II. Aluminum-
stimulated excretion of malic acid from root apices. Plant Physiol 103:695-702
Ezaki B, Gardner RC, Ezaki Y, Matsumoto H (2000) Expression of aluminum-induced genes in transgenic
Arabidopsis plants can ameliorate aluminum stress and/or oxidative stress. Plant Physiol 122:657-665
Kochian LV (1995) Cellular mechanisms of aluminum toxicity and resistance in plants. Annu Rev Plant Physiol
Plant Mol Biol 46: 237-260
Li XF, Ma JF, Matsumoto H (2002) Aluminum-induced secretion of both citrate and malate in rye. Plant and
Soil 242:235-243
Ma JF, Hiradate S, Matsumoto H (1998) High aluminum resistance in buckwheat. II. Oxalic acid detoxifies
aluminum internally. Plant Physiol 117:753-759
Matsumoto, H (2000) Cell biology of aluminum toxicity and tolerance in higher plants. Intl Rev Cytol 200:1-46
RM569
RM545
RM517
RM251
RM232
43.1
14.5
38.1
36.1
MALATE
th
Miftahudin, Scoles GJ, Gustafson JP (2004) Development of PCR-based codominant markers flanking the Alt3
gene ini rye. Genome 47:231-238
Nguyen VT, Burow MD, Nguyen HT, Le BT, Le TD, Peterson AH (2001) Molecular mapping of genes
conferring aluminum tolerance in rice (Oryza sativa L.). Theor Appl Genet 102:1002-1010
Pellet DM, Grunes DL, Kochian LV (1995) Organic acid exudation as an aluminum-tolerance mechanism in
maize (Zea mays L) Plant 196:788-795
Ryan PR, Delhaize E, Randall PJ (1995) Characterization of Al-stimulated efflux of malate from the apices of
Al-tolerant wheat roots. Planta 196:103-110
Taylor GJ (1991) Current views of the aluminum stress response: The physiological basis of tolerance. Curr
Topics Plant Biochem Physiol 10:57-93

th
th
Responses of Nutrient Efficient Maize Genotypes to Bio-fertilizer
at Low Chemical Fertilizer Doses

Marlin Sefrila
a
, Munandar
a
, Renih Hayati
a,*
, Sabaruddin
a

a
Plant Science Department, Graduate School, Sriwijaya University,
Jl Padang Selasa No 524, Bukit Besar, Palembang, 30139, Indonesia
* Corresponding author: Tel.: +62 711 354222; fax: +62 711 317202
[email protected]

Abstract

High dose of chemical fertilizer is usually required to obtain high maize (Zea mays L.) yield. Bio-fertilizer
application in combination with nutrient efficient genotype was expected to reduce the chemical fertilizer need
without reducing the yield. The objective of the research was to evaluate the responses of nutrient efficient
genotypes to bio-fertilizer at low chemical fertilizer doses. The field experiment was conducted at Agro Techno
Park (ATP), South Sumatra. The treatments were arranged in Split-Split-Plot Design with three replications. The
main plots were chemical fertilizer doses, which were 25, 50, and 100 % of standard dose at ATP (400, 100, and
50 kg ha
-1
Urea, SP-36, and KCl, respectively). The sub-plots were nutrient efficient genotypes (B41, L167, and
S219), and hybrid B 816 as comparison. The sub-sub-plots consisted of treatments with or without bio-fertilizers.
The bio-fertilizer (10 ml L
-1
) was sprayed to the soil around the plants at 2, 4, 6, and 8 weeks after sowing. The
yields of nutrient efficient genotypes (5.23 to 7.89 ton ha
-1
) were comparable to the yield of B 816 (6.58 to 7.62
ton ha
-1
) at all chemical fertilizer doses without bio-fertilizer. The genotypes responded differently to the bio-
fertilizer application. Supply of bio-fertilizer at chemical fertilizer doses of 50 % tended to increase the yield of B
41 up to 16 % of its yield at 100 % chemical fertilizer dose without biofertilizer. This suggested that the
chemical fertilizer dose can be reduced by 50 % only for B 41.

Key words: bio-fertilizer, low input, maize, nutrient efficiency

Introduction

High dose of chemical fertilizer is usually required to obtain high maize yield, especially for
South Sumatra soil with deficiency of macro elements problem due to low soil pH (< 5.6). However,
poor farmers often cannot afford it. According to Djafar and Halimi (1998), the farmers in South
Sumatra only apply the chemical fertilizer with sub optimum rate for maize production (75, 50, and
50 kg ha
-1
Urea, SP 36, and KCl, respectively). An excessive use of chemical fertilizer can also
cause an environmental problem. Nutrient efficient maize genotype in combination with bio-fertilizer
may offer an alternative to overcome the problem.
Nutrient efficient genotype has the ability to produce a higher yield than other genotypes
under low nutrient supply (Presterl et al., 2003; Worku et al., 2007). Department Agronomy,
Sriwijaya University is now in the process of developing the nutrient efficient open pollinated maize
genotypes and B 41, S 219, and L 164 used in this experiment are some of them (Munandar et al.,
2010).
Bio-fertilizer usually contains microorganisms having specific function such as Azospirillum
to fix N2 and P solubilizing bacteria to solubilize P from the soil and fertilizer to be available to the
plants (Saraswati & Sumarno, 2008). Several researchers had conducted the experiments to
evaluate the responses of various plants such as young Robusta coffee (Junaedi et al., 1999),
soybean (Noor, 2003; Totok & Rahayu, 2007), and turfgrass (Guntoro et al., 2007) to the bio-
fertilizer application, but the results were still inconsistent. Further research is still needed in this
area.
th
Bio-fertilizer application in combination with nutrient efficient genotypes in this research
was expected to reduce the chemical fertilizer supply up to 25% of the standard dose without
reducing yield. The objective was to evaluate the responses of several nutrient efficient genotypes
compared to the hybrid to bio-fertilizer application especially at low chemical fertilizer rate.


The experiment was conducted at Agro Techno Park (ATP), South Sumatra in January to
April 2011. The soil was dominated by sand (69.91%) with 4.4 pH, 28.3 g kg
-1
C organic matter, 2.1
g kg
-1
N, 59.1 mg kg
-1
P-Bray, and 0.19 c mol kg
-1
exchangeable K. The experimental design was
Split-split-Plot with three replications. The main plot, the chemical fertilizer doses, consisted of 25,
50, and 100 % of the standard rate at ATP (400, 100, and 50 kg ha
-1
Urea, SP 36, and KCl,
respectively). The split plot was the genotypes which consisted of B 41, S 219, and L164 as the
nutrient efficient genotypes and Hybrid B 816 as comparison. The split-split plots were treatments
with and without bio fertilizers which consisted of two types, Subur (bio fertilizer 1), and EM 4 (bio
fertilizer 2). Seeds were sown manually with 70 cm x 25 cm row spacing and two seeds per hole.
Plants were thinned into one plant per hole at one week after sowing (WAS), so in each 2.8 m x 2.5
m sub-sub plot contained 40 plants. Chemical fertilizers (1/3 of Urea, SP 36, and KCl) were applied
at sowing and the rest of Urea was applied at 4 WAS. Organic fertilizer (10 ton ha
-1
) was applied at
2 WAS. Bio-fertilizer (10 ml L
-1
) was sprayed to the soil at 2, 4, 6, and 8 WAS as recommended
application time. Water was sprayed to the soil around the plants for treatment without biofertilizer.
All ears of each sub-sub-plot were harvested at harvest maturity, counted, and air dried in
the drying room for two weeks, weighted .and converted into yield (ton ha
-1
). Ears from three
sample plants (randomly chosen) per plot were weighted and the average was used to get the ear
weight per plant data.


The yield of nutrient efficient genotypes (B 41, S 219, and L 164) at all chemical fertilizer
doses without bio-fertilizer (5.23 to 7.89 ton ha
-1
) was comparable to the yield of hybrid B 816 (6.58
to 7.62 ton ha
-1
). Among the nutrient efficient genotypes, S 219 had the lowest yield followed by B
41 and L 164 genotypes, especially at 25 and 50% chemical doses (Table 1). This suggested that L
164 genotype in this experiment had the highest nutrient use efficiency compared to B 41 and S
219 genotypes. The result was consistent with the previous experiment (Munandar et al., 2010).
The yield or ear weight (ton ha
-1
) significantly correlated with ear weight plant
-1
(r = 0.54*).
Bio-fertilizer application had no significant effect on yield (data not presented), but tended
to increase yield only for B 41 and S 219 genotypes especially for Bio-fertilizer 1 (Table 1). The
yield of B 41 at 50 % chemical fertilizer dose was 94 % of its own yield at 100 % chemical fertilizer
rate without bio-fertilizer. The yield of B 41 genotype increased only 16 % by the application of Bio-
fertilizer 1 or 9 % by bio-fertilizer 2 (Table 1). The yield of S 219 genotype increased 8 to 11 % at 25
and 50 % chemical fertilizer dose, respectively, but the values after the addition of bio-fertilizers
were still lower than the yield at 100 % chemical fertilizer dose without bio-fertilizer. The data
suggests that the chemical fertilizer dose can be reduced by 50 % with the application of bio-
fertilizer only for B 41 genotype. The effect of genotype on yield was higher than the bio-fertilizer
(data not presented).
The L 164 genotype and hybrid B 816 did not give positive responses to both bio-fertilizers
probably because their yields at all chemical fertilizer doses without bio-fertilizer were higher than
the yields of B 41 and S 219. It indicated that L 164 genotype and hybrid B 816 had an ability to
th
take up or use nutrient more efficient than that of the B 41 and S 219 genotypes as suggested by
Worku et al.( 2007).
The bio-fertilizers used in this experiment contained microorganisms to fix N
2
and to
solubilize P, but the P Bray of the soil was high. Therefore, small increase in yield of B 41 and S
219 genotypes by application of bio-fertilizer probably related to a better N use efficiency than P
efficiency of the genotypes.
In conclusion, genotypes responded differently to the bio-fertilizers. Supply of bio-fertilizer
at 50% of chemical fertilizer doses tended to increase the yield of B 41 genotype up to 16% of
100% chemical fertilizer dose without bio-fertilizer. This suggested that the chemical fertilizer dose
can be reduced by 50% without reducing yield only for B 41 genotype.

Table 1. Yield (ear weight) of the nutrient efficient and hybrid genotypes as affected by bio and chemical
fertilizers

Genotypes
Chemical Fertilizer (% of standard rate) ton ha
-1

mean
25 50 100
B 41 without biofertilizer 6.35 (101) 5.94 (94) 6.32 (100) 6.20
+ Bio fertilizer 1 5.84 (92) 6.96 (110) 6.89 (109) 6.56
+ Bio fertilizer 2 6.40 (101) 6.48 (103) 6.66 (105) 6.51
S 219 without biofertilizer 5.23 (79) 5.49 (83) 6.61 (100) 5.78
+ Bio fertilizer 1 5.74 (87) 6.22 (94) 6.58 (100) 6.18
+ Bio fertilizer 2 4.48 (68) 5.92 (90) 6.60 (100) 5.67
L 164 without biofertilizer 7.12 6.83 7.89 7.28
+ Bio fertilizer 1 6.37 6.23 7.44 6.68
+ Bio fertilizer 2 5.94 6.53 7.06 6.51
Hybrid B 816 without bioertilizer 6.58 7.62 7.19 7.13
+ Bio fertilizer 1 6.25 6.36 6.38 6.33
+ Bio fertilizer 2 6.03 7.05 6.83 6.64
Note: Number in parentheses is the relative to its yield at 100 % without bio-fertilizer

References

Djafar, Z.R., and E.S. Halimi. 1998. Increasing the corn production in South Sumatra. J Tan Tropika. 1:128-
134.
Guntoro, D., B.S. Purwoko, and R.G. Hurriyah. 2007. Growth, nutrient uptake, and quality of turfgrass at some
dosages of mycorrhiza application. Bul. Agron. 35:142-147.
Junaedi, A., A. Wachjar, and A. Rahman. 1999. The effect of biofertilizer on the growth of young coffee (Cofee
canephora Pierre ex Froehner) var robusta. Bul. Agron. 27:12-17.
Munandar, R. Hayati, H. Adam, Sabaruddin, and R.J. Anjani. 2010. Developing nutrient efficient maize
genotypes in marginal land using recurrent selection. Proceeding of National Seminar Polinela,
Lampung. Pp. 674-689.
Noor, A. 2003. The effect of rock phosphate and combination of phosphate-solubilizingBacteria and farm yard
manure on soil available P and growth of soybean on Ultisols. Bul. Agron. 31:100-106.
Saraswati, R. and Sumarno. 2008. Application of soil microorganisms as component of agriculture technology.
Iptek. Tan. Pangan 3:41.

th
th
Kinetin and Calcium Pantothenate Effects on Shoot Multiplication in
In Vitro Cultured Cassava Var. Adira 2 and Adira 4

Nurul Khumaida
a,*
, Sintho Wahyuning Ardie
a
, Candra Catur Nugroho
a
, Suwarto
a

a
* Corresponding author: Department of Agronomy and Horticulture, Faculty of Agriculture,
Bogor Agricultural University,
Jl. Meranti, Kampus IPB Darmaga, Bogor 16680, Indonesia.
Tel.: +62 251 862 9353; fax: +62 251 862 9353.
[email protected]

Abstract

Cassava (Manihot esculenta Crantz.) is one of largest carbohydrate sources in the world which also potentially
developed as the source of bio-energy and raw materials for severals industries. As the demand for cassava is
increasing, it is very important to supply the true-to-type cassava seedling continuously. In vitro propagation is
one advanced technique that can be applied to meet the increasing demand of cassava seedling. The objective
of the research was to study the effect of kinetin and Calcium Pantothenate (CaP) concentration on shoot
multiplication of in vitro cultured cassava var. Adira 2 and Adira 4. This research was conducted in a completely
randomized design with two factors. The first factor was kinetin concentration (0; 1; 1.5; and 3 ppm) and the
second factor was concentration of CaP (0; 1; and 2 ppm) used in combination. The results showed that MS
medium supplemented with 1 ppm CaP and 1.5 ppm kinetin promoted the growth of cassava explants of Adira 2
variety until 4 Weeks After Treatment (WAT). However, for longer culture period MS medium containing 3 ppm
of BAP was better to support the explants growth. MS Medium containing 1 ppm of CaP and 3 ppm of kinetin
promoted the growth of Adira 4 variety until 4 WAT. However, for longer culture period MS medium containing 2
ppm of CaP and 3 ppm of kinetin was better to support the explants growth. The highest shoot multiplication rate
for 20 weeks old plantlets of Adira 2 and Adira 4 varieties was obtained at MS medium containing 3 ppm of BAP.

Keywords: calcium pantothenate, cassava, kinetin, shoot multiplication

Introduction

Cassava (Manihot esculenta Crantz) is the third largest source of carbohydrate for human
consumption in the world. It is the principal carbohydrate source for more than 500 million people in
the tropical world. Cassava plays a famine prevention role wherever it is cultivated widely. Cassava
has adaptability to a range of climatic and edaphic conditions including tolerance to drought, to
some pests and diseases relative to other crops, and confers a comparative advantage on cassava
under conditions of famine against alternative crops.
More recently, cassava has gained importance as a possible fuel commodity not only in
Indonesia but also in the Philippines, China, Thailand, and other countries which have more
advanced national bio-fuel programs. In situations where water availability is limited (i.e. not enough
for the cultivation of sugar cane), cassava is the preferred feedstock for ethanol production.
However, cassava-based industries are facing the main problem of cassava availability in amount
and continuity (Suryana, 2009). Therefore, in order to meet the large demand of cassava, farmers
need large amount of good quality cassava seedling in a relaitvely short time.
In general, cassava is propagated by stem cutting. Eventhough stem cutting is easy to be
done and relatively cheap, it is not always available when needed and it is difficult to assure to have
the true to type seedling. In vitro technique is one method for mass propagation can be applied for
rapid mass propagation of cassava seedlings. Research in cassava shoot multiplication and the
induction of embryogenic callus had been done recently (Guohua, 1998; Sudarmonowati et al.,
th
2002; Onuoch and Onwubiku, 2007). Previous results showed that cassava Mentega formed the
highest shoot formation when cultured in MS medium containing 2 ppm of BAP (Sudarmonowati et
al., 2002). In other varieties, Fauzi (2010) found that standard MS medium containing 1.5 ppm of
BAP was the most effective medium for shoot multiplication. The objective of this research was to
study the effect of Kinetin and Calcium panthothenate (Ca-P) addition in the shoot multiplication of
Adira 2 and Adira 4 cassava varieties.


The research was conducted from January 2010 to January 2011 at Plant Biotechnology
Laboratory, Department of Agronomy and Horticulture, Agriculture Faculty, Bogor Agricultural
University. This research was consisted of two separated experiments differed in the cassava
variety used as explants (Adira 2 and Adira 4 varieties). The experiment was arranged in
Randomized Block Design with two factors and ten replicates. The two factors were kinetin and
Calcium panthothenate (Ca-P) concentrations. There were four levels of kinetin concentrations (0;
1; 1.5; and 3 ppm), and three levels of Ca-P concentrations (0; 1; and 2 ppm). A control experiment
was made using standard MS medium with an addition of 3 ppm BAP. Each replicate consisted of
one bottle culture with one explants.
Plant material used was one node of axillary shoot from in vitro culture of Adira 2 and Adira 4
cassava varieties provided by Indonesian Center for Agricultural Biotechnology and Genetic
Resource Research and Development (ICABIOGRD). MS medium was used as basic medium of all
treatments. Surface sterilization was conducted by dipping the axillary shoots in Agrept (2 g L
-1
) and
Dithane (2 g L
-1
) solution for 2 h, and consecutively into Chloramfenicol (2 g L
-1
) solution overnight.
Sterilization by dipping in 10% NaClO solution for 5 min, then into 5% NaClO for 2 min was
conducted in the laminar air flow cabinet. Sterilized shoots were planted in the precondition medium
with 4 -5 explants in each bottle for 4 weeks. Explants used for experiment were micro cutting with
single node of cassava (approximately 1-3 mm in length) cultured in the precondition medium.
Those explants were transferred into MS medium containing kinetin or Ca-P according the
treatments.
Planted explants were cultured in the dark for one week to induce shoot initiation. After that,
cultures were transferred into 24 h light condition with 21
o
C for 9 weeks. Observations were
conducted on in vitro culture and acclimatized plants. On the in vitro culture, the first shoot formed
and the time of callus formation were observed daily. Percentage of callus formation (%), number
and percentage explants with shoot (%), number of shoot per explants, callus diameter (mm), callus
color, structure of callus, length of shoot (mm), shoot morphology, number of leaves, number of
explants with root, number of roots, and number of nodes were observed weekly until 10 Weeks
After Planting (WAP). Data was test for normality then tested with F-test at = 5%. Data with
significant difference was tested with Duncan Multiple Range Test.


The use of Ca-P in several concentrations only affected the callus diameter of Adira 2
variety, while kinetin addition significantly affected number of shoot and callus diameter of Adira 2
and Adira 4 varieties. Interaction between Ca-P and kinetin concentration only affected the callus
diameter of Adira 4 variety. The contamination rate in this research was relatively low for Adira 2
variety (2.12%) and Adira4 variety (1.77%), respectively. Most of the contamination in the culture
was caused by bacteria. Fungi contaminated the culture media in a lower level than bacteria.
As shown in Table 1, percentage of explants with shoots of Adira2 variety were higher
except for three combination showing lower percentage (less than 50%) that were 1.5 ppm of
th
kinetin, 1 ppm of CaP, and 2 ppm CaP. All treatment combination did not significantly affect the
shoot formation. In the other hand, medium containing 3 ppm of BAP resulted in 100% callus
formation. Some treatments that failed to induce callus formation were in medium without kinetin or
low kinetin concentration (less than 1.5 ppm). For Adira 4 variety, the highest percentage of
explants with shoots was resulted in medium containing 0.5 ppm of kinetin. In general, percentage
of explants with shoot was relatively high (more than 50 %) for all treatments, except for medium
containing 3 ppm of kinetin (44.44 %). The highest number of callus formed was achieved in
medium containing high level of cytokinin (3 ppm BAP and 3 ppm kinetin). In contrary, the root
formation was inhibited with the presence of high level of cytokinin. Root formation was induced in
medium containing low concentration of cytokinin.

Table 1. Percentage of shoot forming explants, callused explants, and rooted explants of Cassava Adira2 and
Adira 4 variety at 10 WAP

At the 1 WAP, shoot of cassava was initiated at the nodes. Number of shoot formed in
every treatment was compared to number of shoot formed in the control treatment (medium
containing 3 ppm BAP, B3) and tested by Dunnet test as shown in Table 2.
Table 2 indicates that every treatments affected number of node when they were
compared to the control medium B3, except for C0K3B3 (9 WAP), C0K3B3 and C1K3B3 (10
WAP). In contrast, for Adira 4 variety none of the treatment affected number of node when
compared to the control medium. Based on the regression analysis, kinetin addition could be
increased above 3 ppm. For Adira 2 variety, the regression equation for shoot formation and kinetin
concentration was linear (y = 0.401x 0.095, R
2
= 0.866). This equation means that every 1 ppm
increase of kinetin concentration would increase shoot formation 0.401 per explants. For Adira4
variety, the regression equation for shoot formation and kinetin concentration was also linear (y =
0.278x + 0.224, R
2
= 0.613). This equation means that every 1 ppm increase of kinetin
concentration would increase shoot formation 0.278 per explants.

Treatment
Adira 2 Adira 4
Shoot forming
explants
Callused
explants
Rooted
explants
Shoot
forming
explants
Callused
explants
Rooted
explants
Ca-P
(ppm)
Kinetin
(ppm)
..%.......................... ..%..........................
0
0 75.00 0.00 75.00 66.67 11.11 44.44
1 50.00 0.00 50.00 57.14 0.00 42.86
1.5 33.33 0.00 0.00 80.00 0.00 40.00
3 100.00 33.33 0.00 44.44 44.44 33.33
1
0 25.00 0.00 75.00 50.00 16.67 50.00
1 50.00 25.00 25.00 77.78 22.22 44.44
1.5 100.00 33.33 33.33 66.67 22.22 22.22
3 75.00 25.00 25.00 77.78 66.67 10.00
2
0 33.33 0.00 33.33 70.00 40.00 50.00
1 75.00 0.00 25.00 71.43 0.00 57.14
1.5 100.00 50.00 100.00 66.67 11.11 33.33
3 100.00 33.33 33.33 60.00 60.00 20.00
3 ppm BAP 100.00 100.00 0.00 75.00 50.00 0.00
th
Table 2. Number of cassava shoot of Adira2 and Adira4 variety in the in vitro culture at 9 and 10 WAP

Treatment combination
Adira 2 Adira 4
Age (WAP) Age (WAP)
9 10 9 10
C0K0-B3 3.75* 3.75* 0.71
ns
0.71
ns

C0K1-B3 4.00* 4.00* 0.88
ns
0.80
ns

C0K1.5-B3 3.00* 4.17* 0.58
ns
0.58
ns

C0K3-B3 2.17
ns
2.17
ns
0.93
ns
0.93
ns

C1K0-B3 4.25* 4.25* 0.75
ns
0.88
ns

C1K1-B3 4.00* 4.00* 0.60
ns
0.60
ns

C1K1.5-B3 4.17* 3.17* 0.71
ns
0.71
ns

C1K3-B3 3.00* 2.75
ns
0.53
ns
0.29
ns

C2K0-B3 4.17* 4.17* 0.48
ns
0.58
ns

C2K1-B3 3.75* 3.75* 0.60
ns
0.66
ns

C2K1.5-B3 3.50* 3.50* 0.71
ns
0.71
ns

C2K3-B3 2.50* 3.50* 1.33
ns
1.23
ns

F test * * * *
Note : Variety was not compared to each other; C0, C1, C2 = 0, 1, 2 ppm CaP, respectively; K0, K1, K1.5, K3 = 0, 1, 1.5, 3 ppm
kinetin, respectively; B3 = MS + 3 ppm BAP; ns = not significant at P = 0.05; * = significantly different (P<0.05)

Table 3. Number of leaf of cassava Adira2 and Adira4 variety at 3, 7, and 10 WAP

Treatment
Adira 2 Adira 4
Age (WAP) Age (WAP)
CaP (ppm) Kinetin (ppm) 3 7 10 3 7 10
0
0
1.25 2.00 b 2.75
0.80 jkl
0.30 0.33
1
1.00 0.33 b 0.00
0.70 jkl
0.33 0.43
1.5
0.50 0.25 b 0.00
0.60 jkl
0.14 0.20
3
1.25 1.33 b 1.33
0.40 jkl
0.22 0.11
1
0
0.25 0.25 b 0.25
1.10 j
1.00 0.67
1
0.50 0.50 b 1.25
1.00 jk
0.67 0.33
1.5
2.00 2.00 b 1.00
1.20 j
0.33 0.44
3
0.50 0.50 b 0.25
1.20 j
1.10 0.56
2
0
0.00 0.00 b 0.00
1.10 j
0.30 0.40
1
1.00 1.25 b 1.25
0.90 jk
0.33 0.57
1.5
1.00 1.67 b 2.50
0.60 jkl
0.20 0.22
3
0.75 1.33 b 1.67
0.00 l
0.70 2.00
3 ppm BAP
1.00 5.50 b 7.50
0.11 kl
0.50 1.00
F test ns * ns * ns ns
Note: Variety was not compared to each other; Numbers followed by the same letter in the same columns are not significantly
different based on DMRT at level = 5%.

Leaf formation of cassava explants started at the 2 WAP. The leaf formation rate was
slower than the leaf senescence rate at the 4 WAP and resulted in the decreased of leaf number in
every observation point. The leaf senescence might be caused by the production of ethylene gas,
nutrient deficiency, and toxicity. Magdalita et al. (1997) found that the accumulation of ethylene
fasten the senescence of leaves in in vitro culture. Nutrient deficiency might caused by longer
th
culture, thus periodically subculture might be needed at 4 WAP. Leaf senescence might be also
caused by endogen auxin-cytokinin imbalance in the plants tissues (Lizawati et al., 2009). As shown
in Table 3, the highest number of leaf for Adira 2 variety at 10 WAP resulted in medium containing 3
ppm of BAP. In contrast, medium containing 1 ppm of kinetin, 1.5 ppm of kinetin, and 2 ppm of CaP
resulted in lowest leaf number (0). The highest number of leaf for Adira 2 variety at 10 WAP
resulted in medium containing 2 ppm of CaP in combination with 3 ppm of kinetin, while medium
containing 1.5 ppm of kinetin resulted in the lowest number of leaf formed.
Shoot multiplication rate could be increased by periodically subculture (Hartmann and
Kester, 1983). In this research, the subculture was done twice. The first subculture was done at 10
WAP, while the second subculture was done 4 weeks after the first subculture. The multiplication
rate for Adira 4 variety was observed only at the first subculture. As shown in Table 4, the highest
multiplication rate was achieved in the medium containing 3 ppm of BAP for both varieties.

Table 4. Shoot multiplication rate of in vitro grown cassava Adira 2 and Adira 4 varieties

Variety
Treatment
Replica
tion
Initial
explants
Initial
shoots
Shoot
first sub-
culture
Shoot
second
sub-
culture
Total number
of Shoot
Kinetin
(ppm)
CaP
(ppm)
Adira 2
0 0 1 1 1 5 2a 8
3 0 1 1 1 3 3b 7
3 0 3 1 5 3 8
Means + Standard deviation 7.50 0.71
1 1 1 1 1 5 3bc 9
1.5 1
1 1 1 2 3
3 2 1 1 1 1 2 4
3 ppm BAP 1 1 7 17 34 58
3 ppm BAP 2 1 2 2 4
Adira 4
1 0 4 1 1 2

3
3 1 7 1 3 4

7
3 1
8 1 2 1

3
0 2 1 1 2 1

3
3 2 3 1 6 8

14
3 2 6 1 6 11

17
3 2 7 1 5 1

6
3 2 9 1 8 1

9
3 ppm BAP 10 1 6 27 33
Note : Variety was not compared to each other; a = sub-cultured to MS0 + 3 ppm kinetin; b = sub-cultured to MS0 + 2 ppm CaP
+ 3 ppm BAP; c = sub-cultured to MS0 + 2 ppm CaP + 3 ppm kinetin

Conclusions

The use of several kinetin concentrations (0; 1; 1.5; dan 3 ppm) gave a positive linear
response to number of shoots for both varieties (Adira 2 and Adira 4). In contrast, concentration of
kinetin had negative linear response to number of roots. Media composition with 1 ppm of CaP in
combination with 3 ppm of kinetin promoted the growth of cassava explants of Adira 4 variety until 4
th
WAT, but for longer culture period MS medium containing 2 ppm of CaP and 3 ppm of kinetin was
better to support the explants growth. The highest shoot multiplication rate was achieved in the
medium containing 3 ppm of BAP for both varieties.

References

Fauzi, AR. 2010. Induksi Multiplikasi Tunas Ubi Kayu (Mannihot esculenta Crantz.) var. Adira 2 secara In Vitro.
Skripsi. Fakultas Pertanian. Institut Pertanian Bogor. Bogor. 67 hal.
Hartmann, H.T. DE. Kester. 1983. Plant propagation, principles, and practice, p. 223-280. In E. Cliffs (ed.).
Prentice-Hall inc. New Jersey.
Guohua, M. 1998. Effects of cytokinins and auxins on cassava shoot organogenesis and somatic
embryogenesis from somatic embryo explants. Plant Cell Tissue Organ Cult. 54:1-7.
Lizawati, T. Novita, R. Purnamaningsih. 2009. Induksi dan multiplikasi tunas jarak pagar (Jatropha curcas L.)
secara in vitro. J. Agron. Indonesia 37: 78-85
Magdalita, PM., DG. Ian, AD. Roderick, WA. Stephen. 1997. Effect of ethylene and culture environment on
development of papaya nodal culture. Plant Cell Tissue Organ Cult. 49:93-100.
Onuoch, CI., NIC Onwubiku. 2007. Micropropagation of cassava (Mannihot esculenta Crantz) using different
concentrations of benzylaminopurine (BAP). J. Engineering Appl. Sci. 2:1229-1231.
Sudarmonowati, E., R. Hartati, T. Taryana. 2002. Produksi Tunas, Regenerasi dan Evaluasi Hasil Ubi Kayu
(Mannihot esculenta) Indonesia Asal Kultur Jaringan di Lapang. Pusat Penelitian Bioteknologi. LIPI:
Cibinong.

th
Wet Injury of Wheat in Upland Field Converted from Paddy Field in Japan

Kentaro Kawaguchi*

Wheat and Barley Research Divison, NARO Institute of Crop Science (NICS),
National Agriculture and Food Research Organization (NARO), Japan
*Corresponding author: Wheat and Barley Research Divison, NARO Institute of Crop Science (NICS),
National Agriculture and Food Research Organization (NARO).
2-1-18, Kannondai, Tsukuba, Ibaraki 305-8518, Japan.
Tel. +81 29 838 8694; Fax. +81 29 838 8694
[email protected]

Abstract

Wheat and barley are very important crops used as staple food and feed. Growth delay or injury of wheat and
barley under waterlogged soils is one of agricultural constraints to be solved. The common symptoms are
germination failure, leaf color degradation, and wilting. Since there are different types of waterlogging conditions,
the mechanisms of injury also varied. However, root sensitivity to low-oxygen atmosphere in soil is critical. Rice
plant has been widely cultivated in Japan. In recent years the agricultural policy enhanced rice-wheat-soybean
rotation using paddy fields for economic reasons. Crop production using paddy fields is thought to be an
important key for sustainable agriculture in eastern Asia but wet injury of wheat usually occurs in the upland
fields converted from paddy fields because of the poor drainage. Under a particular case, a phenomenon called
ground subsidence due to the earthquake induced wet injury in this year. The most popular measure to mitigate
the waterlogging damage on farm level is the field management to facilitate drainage. In addition, we have great
hopes for establishing tolerant varieties; however, such commercial one is not yet obtained by traditional
breeding. We are now engaged on an innovative research project about root aerenchyma which is thought to
facilitate gas exchange between root and aerial parts of plants. We hypothesized its modification could change
the sensitivity of root to low-oxygen. The project plan was; i) to investigate anatomical and physiological basis of
aerenchyma formation in the recipient wheat cv. Bobwhite. ii) to establish transgenic wheat lines using several
candidate genes for root aerenchyma formation. iii) to analyze function of the genes using the transgenic
Bobwhite lines.

Keywords: aerenchyma, barley, subsidence, waterlogging, wheat

Introduction

The main production areas of wheat in Japan are in Hokkaido, Kanto and Kyushu district.
Except in Hokkaido, they have relatively high precipitation. It is over one thousand mm a year.
Sowing and harvest of wheat often coincide with the two rain periods, we call them Akisame
(autumnal rain in September and November) and Baiu (rainy season in June). Moreover, wheat is
widely grown in upland fields converted from rice paddy fields in Japan. The main reason to
cultivate wheat instead of rice is due to decline of the amount of rice consumption. Full efficient
utilization of rice paddy fields is one of the main policies of the Japanese government. Average of
wheat acreage in recent 10 years is 210 thousand ha and the over half of the acreage is the rice
fields. Oyanagi (2008) reported that about 20% of the wheat acreage is affected by waterlogging.
Wet injury usually occurs in the converted fields because of the poor drainage and it
causes severe damage on the grain yields as well as their quality. One of the causes of the wet
injury is shortage of oxygen in the low layer, where the wheat roots develope and obtain oxygen to
grow. The most effective way to prevent wet injury is the field management for well drainage, for
example, ditch making and raised bed farming, etc., however, the economic cost for such field
management is relatively high in the farm level. Therefore, we develop new lines of wheat having
high tolerance to wet soil.
th
To overcome the agricultural constraint, understanding of the mechanisms of wet injury
and tolerance in wheat is essential. In our study, first, we characterized wheat growth under wet
conditions in farmers fields and in our experimental paddy fields. The results showed that i) there
were high correlations between yield and soil moisture in the farm level and ii) wheat growth
suffered from wet stress from the early development under the condition of paddy field. Second, we
focused on root aerenchyma. Aerenchyma is thought to be enhancing gas exchange between
subterranean part (root) and aerial part (shoot) of plant tissues. Therefore, root aerenchyma is one
of the important traits to contribute wet tolerance of plants. To investigate the basic nature of root
aerenchyma formation during early development of wheat, we examined when and where root
aerenchyma were formed in the wheat seminal root under waterlogging condition using a plant pot
system.Third, we recently studied the strategy to improve wheat using modern biotechnology.


Field experiment
Wheat (Triticum aestivum L.) cultivars. Bobwhite (Mexican cultivar), Norin 61 (Japanese
cultivar), Iskra and NS-302 (Yugoslavian cultivars) were used in this experiment. The latter two
were selected as candidates for high tolerant cultivars (Dr Sato, unpublished data). Norin 61 is the
major cultivar in Japan except in Hokkaido region. Bobwhite is often used as a host for establishing
fertile transgenic by means of particle bombardment in wheat. Experimental fields were located at
Yawara, Tsukuba-mirai city, Ibaraki, Japan. Five are area each of contiguous two upland fields
converted from paddy fields were used. One was used under non-tilling cultivation as control plot
and the other was used after soil puddling as wet treatment plot. Wheat seeds were sown with 70
cm rows on 30
th
October, 2009 and 10
th
November, 2010. Fertilizers (6, 9 and 6 kg/10a each as N,
P
2
O
5
and K
2
O) was applied at ten days before sowing. Growth characters were monitored in 3
weeks interval. The soil water contents were measured by TDR-method (Time Domain
Feflectometry) using a HydroSense CD620 display and CS620 sensor with a 12-cm probe
(Campbell Scientific Australia Pty. Ltd., Thuringowa Central, Australia) in the top 12 cm of the soil.
The soils redox potentials at 10cm depth were recorded using an Eh meter (PRN-41, Fujiwara
Scientific Co.LTD., Tokyo, Japan) with a reference electrode.

Pot experiment for aerenchyma study
Wheat cv. Bobwhite line SH 98 26 was used. Three seeds were sown at a 3-cm depth in
each of 27 soil-filled pots (Fujiwara Scientific, Tokyo, Japan; 1/5000a deep type Wagner pot, 30 cm
height x 15.9 cm inner diameter). The wheat plants were grown in a greenhouse maintained at a
temperature of approximately 20C day/night, with natural light. Water treatments were imposed to
5 d old seedlings: (i) control, with a well-drained; (ii) T-15 treatment, the water level was maintained
at 15 cm below the soil surface, and (iii) T+3 treatment, the water level was maintained at 3 cm
above the soil surface. The O
2
concentrations were recorded at a 14 cm depth in the soil using an
OXY-10 O
2
-sensor (PreSens Precision Sensing GmbH, Regensburg, Germany). Transverse cross-
sections were obtained from primary seminal roots using a D.S.K. Microslicer (DTK-1000, Dosaka
EM Co. Ltd., Kyoto, Japan). The sections were examined and photographed with a light microscope
equipped with a camera (BX51 microscope and DP72 camera, Olympus Co. Ltd., Tokyo, Japan) at
10 magnification.

th

Growth of 4 cultivars of wheat in the experimental fields
The soil conditions in the experimental fields were measured. Ground water levels were
almost less than 75 cm below the soil surface during the entire experiment period. Soil water
contents were higher in puddling plot than that in control plot until April 19. Redox potentials in the
soil were constantly over +500 mV and showed no significant difference between the plots. The
plant height and dry weight were significantly affected by puddling (wet) treatment (Figures 1 and 2
show the results of 2009 2010 season). Similar tendency was observed in the repeated testing in
the next cropping season of wheat. Puddling/Control ratio in dry weight was very low (20%) at
young (on 17 February) and was gradually recovered (80%) at ripening (on 13 May). These results
indicated that wheat suffered from wet stress since their early stage of development and suggested
that high tolerance to wet conditions at the seedling stage is important for wheat production in
paddy fields in Japan.

Figure 1. Changes in the plant height of 4 cultivars of wheat under control condition (solid line) and puddling
(wet) condition (dashed line) in 2009 2010 season.

Figure 2. Dry weight of wheat plants (aerial part only) under control condition (gray bar) and puddling (wet)
condition (black bar) in 2009 -2010 season.

th
Growth and root aerenchyma formation of wheat in pot system
The soil conditions in the plant pot were measured by TDR-method. Under the control, T-
15, and T+3, the soil water contents were 12-14; 23-27; and 74-82%, respectively. The O
2

concentrations after 72 h in T-15 soil decreased from the control soil 18.7 to 10.1%, whereas that in
T+3 soil decreased to 4.9%. While the redox potential in the control soil remained around +400 mV,
the values in the T-15 and T+3 soils were about +360 and +290 mV, respectively, after 72 h
treatment. These results showed that the soil conditions in T-15 and T+3 became hypoxic in order
of water depth during waterlogging treatment.
The length of primary seminal roots and the position of aerenchyma were schematically
drawn in Figure 3. The root length was reduced by 25% in the T+3 plants. The reduction of seminal
root dry mass was 12.5% in T-15 and 31% in T+3 plants, respectively. For the aerial parts, the
plants did not show significant difference (data not shown). Wheat primary seminal roots showed no
aerenchyma in our control condition. Aerenchyma was appeared after 48 h under T+3 and after 72
h under T-15 waterlogging conditions, respectively, at 2 to 5 cm behind the root tip. The
aerenchyma in T+3 plants extended to 2-10 cm behind the tip at 72 h waterlogging.

24 h waterlogging

48 h waterlogging

72 h waterlogging

Base C

T-15

T+3

C

T-15

T+3

C

T-15

T+3

0 cm 0

0

0 0 cm 0

0

0 0 cm 0

0

0 0 cm
3 cm 0

0

0 3 cm 0

0

0 3 cm 0

0

0 3 cm
5 cm 0

0

0 5 cm 0

0

0 5 cm 0

0

5 5 cm

5 cm 0

0

0 10 cm 0

0

7 15 cm 0

0

9 10 cm
2 cm 0

0

0 5 cm 0

0

9 10 cm 0

7

9 5 cm

Tip

Tip

Tip 2 cm 0

1

9 5 cm 0

9

9 2 cm

Tip

Tip

Tip 2 cm 0

9

Tip

Tip

Tip

Root
length
16
0.7
cm

15
0.7
cm

14
0.8
cm

18
0.7
cm

17
0.8
cm

15
0.8
cm

23
0.4
cm

23
0.4
cm

17
0.8
cm

n=9

n=9

n=9

n=9

n=9

n=9

n=9

n=9

n=9

Numbers of root sections with developing aerenchyma are indicated at the sampling position. Roots (n=9) were tested. Black
background indicates aerenchyma formation in more than half number of the nine sections.

Figure 3. Aerenchyma formation in the seminal root of wheat seedlings under waterlogging conditions.

Our results provide basic information on the aerenchyma formation process in seminal
roots of wheat. To our knowledge, this is the first report to describe the time of the aerenchyma
formation in wheat seminal roots under hypoxic conditions (Haque et al. 2010). The development
nature of aerenchyma, such as the formation timing, might be similar in part among several upland
crops. Root aerenchyma can be seen within 48 h after the initiation of hypoxia in the seminal (our
study) and adventitious roots (Malik et al. 2003) in wheat. In maize, aerenchyma formation in the
seminal (Gunawardena et al. 2001) and adventitious roots (Drew et al. 1981) is induced by hypoxia
within a few days. Thus, wheat requires several days to form aerenchyma by waterlogging stress,
while rice plant constitutively forms well developed aerenchyma in their roots. Such different ability
to form aerenchyma among plant species may be one of the important keys to determine their
adaptive nature to water.
Wheat plants grown in our pot system can be used for analyzing the molecular and
physiological mechanisms of aerenchyma formation. Proteome analysis using the wheat seminal
root showed that 10 candidates of proteins would be associated with the metabolism during root
th
development under hypoxia (Haque et al. 2011). Elucidation of the protein function during
aerenchyma formation is a next step of this study.

Future direction
Wheat cv. Bobwhite line SH 98 26 is known to be one of the most useful recipients for
producing transgenic wheat lines (Pellegrineschi et al. 2002). Therefore, the information obtained
from this study will be useful not only for understanding the basic nature of aerenchyma formation,
but also for efforts to improve aerenchyma formation, including the creation of transgenic plants. In
fact, the transgene approach in our experiment showed the ability satisfactorily on the investigation
of seed dormancy of wheat and the related gene (Nakamura et al. 2011). Introducing genes can be
widely selected from various plant species, including rice and teosinte, etc., which have high
capacities to form aerenchyma (Nakazono et al. 2011 in this session, Mano and Omori 2009).

Acknowledgements

The author wish to thank the International Maize and Wheat Improvement Center (CIMMYT), Mexico
for providing seeds of wheat cv. Bobwhite SH 98 26 and the National Institute of Agrobiological Sciences (NIAS)
Genebank for supplying seeds of wheat cv. Iskra and NS-302. I would like to express my thanks to Drs. M.
Nakazono, Y. Mano and S. Shimamura for their valuable suggestions and critical comments to this study. I also
thank Mr. S Hamada for his skillful management of the field experiment. All of the achievements reported here
were produced through the collaborative investigation with my colleagues, Drs A. Oyanagi, F. Abe, Md Emdadul
Haque and M. Mori in NICS. The research was supported by a grant-in-aid from the Bio-oriented Technology
Research Advancement Institution (Promotion of Basic Research Activities for Innovative Biosciences, No. H20 /
seeds-01-01).

References

Drew MC, MB Jackson, SC Giffard and R Campbell. 1981. Inhibition by silver ions of gas space (aerenchyma)
formation in adventitious roots of Zea mays L. subjected to exogenous ethylene or to oxygen deficiency.
Planta 153: 217-224.
Gunawardena AHLAN, DM Pearce, MB Jackson, CR Hawes and DE Evans. 2001. Characterisation of
programmed cell death during aerenchyma formation induced by ethylene or hypoxia in roots of maize
(Zea mays L.). Planta 212: 205-214.
Haque ME, F Abe and K Kawaguchi. 2010. Formation and extension of lysigenous aerenchyma in seminal root
cortex of spring wheat (Triticum aestivum cv. Bobwhite line SH 98 26) seedlings under different
strengths of waterlogging. Plant Root 4: 31-39.
Haque ME, K Kawaguchi and S Komatsu. 2011. Analysis of proteins in aerenchymatous seminal roots of wheat
grown in hypoxic soils under waterlogged conditions. Protein and Peptide Letters 18: 912-924.
Malik AI, TD Colmer, H Lambers and M Schortemeyer. 2003. Aerenchyma formation and radial O
2
loss along
adventitious roots of wheat with only the apical root portion exposed to O
2
deficiency. Plant Cell Environ.
26: 1713-1722.
Mano Y and F Omori. 2009. High-density linkage map around the root aerenchyma locus Qaer1.06 in the
backcross populations of maize Mi29 teosinte Zea nicaraguensis. Breed. Sci. 59: 427-433.
Nakamura S, F Abe, H Kawahigashi, K Nakazono, A Tagiri, T Matsumoto, S Utsugi, T Ogawa, H Handa, H
Ishida, M Mori, K Kawaura, Y Ogihara and H Miura. 2011. Wheat homolog of MOTHER OF FT AND
TFL1 acts in the regulation of germination. Plant Cell online publication, DOI 10.1105/tpc.111.088492.
Nakazono M, T Yamauchi, R. Imene, H. Takahashi, T Abiko, S Nishiuchi, S Yamazaki, K Shiono. 2011. Studies
on molecular mechanism of formations of aerenchyma and a barrier to radial oxygen loss in crops under
waterlogged conditions. In this proceedings.
Oyanagi A. 2008. Relationship of growth variability, with ground level and soil water content in a large paddy
field in Inashiki-city, Ibaraki-prefecture in 2007-Wet injury of wheat. Jpn. J. Crop. Sci. 77: 511-515. (in
Japanese with English abstract)
th
Pellegrineschi A, LM Noguera, B Skovmand, RM Brito, L Velazquez, MM Salgado, R Hernandez, M Warburton,
D Hoisington. 2002. Identification of highly transformable wheat genotypes for mass production of fertile
transgenic plants. Genome 45: 421-430.

th
Roles of Root System Development and Function in the Growth and Yield
under Waterlogged Condition in Common Wheat

Tomohito Hayashi
a
, Tomofumi Yoshida
b
, Kiyoshi Fujii
bc
, Takako Tsuji
b
,
Yurie Okada
a
, Eriko Hayashi
a
, Akira Yamauchi
a

a
Graduate School of Bioagricultural Sciences, Nagoya University, Japan
b
Aichi Prefecture Agricultural Research Center, Aichi, Japan
c
Agricultural Production Division, Aichi Prefectural Government, Aichi, Japan
*Corresponding author: Graduate School of Bioagricultural Science, Nagoya University,
Nagoya 464-8601, Japan
[email protected]

Abstract

Waterlogging stress substantially reduces the productivity of common wheat. Unavailability of oxygen to the
roots is the major growth-limiting factor for plants exposed to waterlogging stress. The development and function
of roots play significant roles in expression of waterlogging tolerance of wheat under such conditions. However,
the mechanism of root function in the waterlogging tolerance is not clear yet. In this study, we, therefore, aimed
to evaluate the roles of root system development and function in the growth and yield of wheat plants that were
exposed to waterlogged condition at jointing stage. This study was conducted in 2009 at Aichi Agricultural
Research Center experimental field. Plants were grown under two different conditions; control for rainfed upland
conditions while in waterlogging treatment (WL), water level was maintained around 5 cm below the soil surface
from jointing stage till maturity. Soil type of this field was andsol. We previously examined a set of germplasm
(144 cultivars) collection, and selected Nishikazekomugi (high waterlogging tolerance), Iwainodaichi (moderate)
and UNICULM (low). Grain yield of Nishikazekomugi in WL was 64% of control, while that of Iwainodaichi and
UNICULM was 38 and 4%, respectively. The cultivars of greater watelogging tolerance further showed the ability
to maintain higher stomatal conductance in WL, which should reflect higher root ability of soil water uptake. In
fact, they showed higher root development as evaluated in total root length. Increase in nodal root porosity of
Nishikazekomugi and Iwainodaichi in response to exposure to WL then contributed to the significant increase in
total root length. Higher root porosity indicates greater root aerenchyma formation in response to waterlogging
stress. These results indicated that the tolerant cultivars had higher ability of aerenchyma formation, which
promoted root system development, and eventually contributed to the increase in shoot dry matter and grain
yield under waterlogged conditions.

Keywords: aerenchyma, common wheat, hydraulic conductivity, porosity, waterlogging tolerance

Introduction

Common wheat is known to be susceptible to waterlogging, and the grain yield
substantially decreases by excess moisture (Oyanagi et al, 2001) in most of the wheat producing
countries such as UK (Belford and Cannel, 1979), Australia (Setter et al., 2009). In Japan, 27% of
wheat-planted field (approximately 57,000 ha) is affected by excess moisture stress (Sakagami et
al., 2010).
When the water table rises to or above the soil surface, roots surrounded by the
waterlogged soil suffer from O
2
deficiency (Jackson et al., 1999; Malik et al., 2003). As one of
mechanisms for waterlogging tolerance, aerenchyma in root provides a low-resistance internal
diffusion pathway to supply O
2
to the root apex (Arikado, 1975; Colmer, 2003; Armstrong and
Armstrong, 2005). Therefore, root aerenchyma formation under waterlogged condition may play
important roles in waterlogging tolerance in wheat (Setter and Waters, 2003). Although wheat plants
generally have low efficiency of root aerenchyma formation (Watkin et al., 1998), genotypic
th
variations in its functional roles in the maintenance of waterlogging tolerance under waterlogged
condition is not yet clear.
In this study, we examined if genotypes with high ability of root aerenchyma formation and
root system development under waterlogging produce high dry matter and yield by evaluating the
impacts of root aerenchyma formation on root development, stomatal conductance, photosynthetic
rate and grain yield under waterlogged conditions, and compared with those under rainfed upland
conditions in the field. Such hypothesis of this study was summarized in Figure 1. The objective of
this study was, therefore, to examine the roles of root aerenchyma formation in the maintenance of
waterlogging tolerance under waterlogged condition in wheat.

Figure 1. Schematic diagram of hypothetical mechanism of waterlogging tolerance in wheat.


Experiment design and Plant materials
A field experiment was conducted at Aichi Agricultural Research Center. Plants were grown
under two different conditions e.i control for rainfed upland conditions while in waterlogging
treatment (WL), water level was maintained around 5 cm below the soil surface from jointing stage
till maturity. Soil type of this field was andsol.
The seeds were sown on December 3, 2008. The waterlogging treatment lasted for 50 days
from April 13 to June 1, 2009. The plants were harvested on June 9, 2009 (188 days after sowing).
Based on the results of our previous study (Hayashi et al., 2008) that examined a set of 144
cultivars collection, we selected three cultivars e.i. Nishikazekomugi (high waterlogging tolerance),
Iwainodaichi (moderate) and UNICULM (low).

Grain Yield
Plants were harvested in six replicates for each cultivar. For shoots, after air-drying for
about three weeks, leaves and stems were oven-dried and weighed, and the grains were threshed.
After the grain moisture content was measured with a grain moisture tester, grains were weighed,
and the yield components were determined.

Root Development
To determine total root length, after the harvest of shoots, roots were sampled in six
replicates for each cultivar. At the end of waterlogging treatment, the roots were sampled with the
round monolith method (Kang et al. 1994) by using stainless cylinder of 15 cm in diameter, and the
soil cores of 20 cm in depth were taken. Soil samples were carefully washed to collect roots. After
removing the debris, the roots were stained and arranged on water in a transparent plastic tray.
They were then scanned to convert to a digitized image, and total root length was determined with
the use of NIH Image ver. 1.62 and Root Length ver. 1.54 (Kimura, 1999).
th
Leaf Water Potential
We measured leaf water potential of the flag leaves in six replicates in each cultivar at -4,
4, 11, 16, 19, 28 and 34 days after the onset of waterlogging treatment. Leaf water potential was
measured with thermocouple psychrometry using sample chambers (Model C-52, Wescor) and a
microvoltmeter (Model HR-33T, Wescor). The sample chambers had been calibrated with NaCl
solution of a known molarity in advance.

Stomatal Conductance and Photosynthetic Rate
We measured stomatal conductance and photosynthetic rate of the flag leaves in three
replicates for each cultivar at -4, 4, 11, 16, 19, 28 and 34 days after the onset of waterlogging
treatment. The measurements were conducted from 800 to 1300 on sunny days at PPFD of 1400
mol m
-2
s
-1
with a portable type apparatus for photosynthesis and transpiration measurements (LI-
6400, LI-COR, Lincoln, NE, USA). Leaf temperature and CO
2
concentrations surrounding leaf was
adjusted to be 281.7 and 400 mol mol
-1
, respectively. Measurement duration average was
about 40 to 60 s. The leaf areas enclosed by chamber were from 3.0 to 6.0 cm
2
.

Root Porosity
We measured porosity of the nodal root in six replicates for each cultivar. Nodal root
porosity was measured 50 days after the onset of waterlogging treatment.The nodal root axis was
used for root porosity measurement following the microbalance method (Visser and Bgenmann,
2003; Suralta et al., 2010).
A 1-cm segment from the middle portion of each root was cut. From each plant (replicate),
sixty 1-cm segments were further sampled. Each 1-cm root segment was cut with a sharp razor
blade and gently blotted by rolling it with a small brush on tissue paper for about 2 s to remove
adherent water. Then, to prevent weight loss by evaporation, the segments were transferred into a
capsule with cover that had been tared on a microbalance. After closing the capsule, the segments
were weighed (w1 in g), transferred to a holder with small vials filled with water, and stored for 30
min. Up to 60 samples were weighed before they were infiltrated with tap water twice under vacuum
for 30 min. After water infiltration, the root segments were blotted again on tissue paper for about 2
s and weighed in a capsule (w2 in g). Using the specific weight (SW) obtained from larger
samples, the porosity was calculated using the formula: Porosity (%; v : v) = 100 (w2 w1)
SW/w2


In this study, we evaluated the roles of root system development and function in the growth
and yield of wheat plants that were exposed to waterlogged condition at jointing stage. Grain yield
of Nishikazekomugi in WL was highest (64% of control), followed by Iwainodaichi (38%), and
UNICULM (4%) (Figure 2). Nodal root porosity of Nishikazekomugi in WL was 284% of control,
while that of Iwainodaichi and UNUCULM was 113% and 44%, respectively (Figure 3). Total root
length of Nishikazekomugi in WL was 104% of control, while that of Iwainodaichi and UNICULM
was 70 and 38%, respectively (Figure 4). These results showed that the cultivar with high porosity
in response to exposure to WL tended to have greater total root length. Specifically, increase in
nodal root porosity of Nishikazekomugi and Iwainodaichi contributed to the significant increase in
total root length. Higher root porosity indicates greater root aerenchyma formation in response to
waterlogging stress.
th

Data are means of 6 replicates. Vertical bar show standard errors (n=6). and represents control and waterlogging conditions,
respectively.

Figure 2. The effect of waterlogging stress on grain yield under rainfed upland (control) and waterlogged
conditions.

Data are means of 60 replicates. Vertical bar show standard errors (n=60). and represents control and waterlogging
conditions, respectively.

Figure 3. The effect of waterlogging stress on nodal root porosity under rainfed upland (control) and waterlogged
conditions.

Data are means of 6 replicates. Vertical bar show standard errors (n=6). and represents control and waterlogging conditions,
respectively.

Figure 4. The effect of waterlogging stress on root length under rainfed upland (control) and waterlogged
conditions.

We also examined the effect of waterlogging stress on leaf water potential, stomatal
conductance and photosynthetic rate. Leaf water potential of Nishikazekomugi maintained to the
level of control for 16 days after waterlogging treatment onset, for 11 days in Iwainodaichi and for 4
days in UNICULM. Stomatal conductance of Nishikazekomugi maintained to the level of control for
16 days, for 16 days in Iwainodaichi and for 11 days in UNICULM. Likewise, photosynthetic rate of
Nishikazekomugi maintained to the level of control for 16 days, for 11 days in Iwainodaichi and for
11 days in UNICULM. As stated above, the cultivars of greater root system development (greater
total root length in WL) further showed the ability to maintain high leaf water potential and stomatal
conductance, which maintained higher photosynthetic rate in WL.
th
These results indicated that the tolerant cultivars have higher ability of aerenchyma
formation, which promotes root system development, and probably root hydraulic conductance,
both of which, through high ability to provide water to shoot, eventually contributed to the increase
in shoot dry matter and grain yield under waterlogged conditions.

References

Arikado H. 1975. Waterlogging tolerance of aerenchyma and crops. Oriental print. Mie. Pp149.
Armstrong J and W Armstrong. 2005. Rice: sulfide-induced barriers to radial oxygen loss, Fe+ and water uptake,
and lateral root emergence. Ann Bot. 96: 625-638.
Belford RK, RQ Cannel. 1979. Effects of waterlogging of winter-wheat prior to emergence on crop establishment
and yield. J Sci Food Agr. 30: 340-340.
Colmer TD. 2003. Aerenchyma and an inducible barrier to radial oxygen loss facilitate root aeration in upland,
paddy and deep-water rice (Oryza sativa L.). Ann Bot. 91: 301-309.
Jackson MB, W Armstrong. 1999. Formation of aerenchyma and the process of plant ventilation in relation to
soil flooding and submergence. Plant Biol. 1: 274-287.
Kang SY, S Morita, K Yamazaki. 1994. Root growth and distribution in some japonica-indica hybrid and japonica
type rice cultivars under field conditions. Jpn J Crop Sci. 63: 118-124
Kimura K, S Kikuchi and S Yamasaki. 1999. Accurate root length measurement by image analysis. Plant Soil.
216: 117-127.
Malik AI, TD Colmer, H Lambers and M Schortemeyer. 2003. Aerenchyma formation and radial O
2
loss along
adventitious roots of wheat with only the apical root portion exposed to O
2
deciency. Plant Cell Environ.
26: 1713-1722.
Oyanagi A, C Kiribuchi-Otobe, T Yanagisawa, S Miura, H Kobayashi and S Muranaka. 2001.Selection of wheat
experimental lines with deep and shallow root systems based on the growth angle of seminal roots. Jpn J
Crop Sci. 70: 400-407.
Sakagami J, M. Nakazono, S. Shimamura, O. Ito, K. Ishizawa. Wetland environment and crops. Youkendo.
Tokyo. Pp139-150.
Setter and Waters. 2003. Review of prospects for germplasm improvement for waterlogging tolerance in wheat,
barley and oats. Plant Soil. 253: 1-34.
Setter T.L, I. Waters, S. K. Sharma, K. N. Singh, N. Kulshreshtha, N. P. S. Yaduvanshi, P. C. Ram, B. N. Singh,
J. Rane, G. MCDonald, H. Khabaz-Saberi, T. B. Biddulph, R. Wilson, I. Barclay, R. MCLean, M. Cakir.
2009. Review of wheat improvement for waterlogging tolerance in Australia and India: the importance of
anaerobiosois and element toxicities associated with different soils. Ann Bot. 103: 221-235.
Suralta RR, Y Inukai, A Yamauchi. 2010. Dry matter production in relation to root plastic development, oxygen
transport, and water uptake of rice under transient soil moisture stresses. Plant Soil. 332: 87-104.
Hayashi T, T Yoshida, K Fujii, T Tsuji and A Yamauchi. 2008. Relationship between root system ability, and
photosynthesis and grain yield under excess soil moisture conditions in wheat. Jpn J Crop Sci. 77 (Extra
issue 2): 254-255.
Visser EJW and GM Bgenmann. 2003. Measurement of porosity in very small samples of plant tissue. Plant
Soil. 253: 81-90
Watkin EJ, C Thomson and Hankgreenway. 1998. Root development and aerenchyma formation in two wheat
cultivars and one triticale cultivar grown in stagnant agar and aerated nutrient solution. Ann Bot. 81: 349-
354.

--- back to Table of Content---
th
th
Growth and Physiological Responses of Sago Palm against Aluminum
Stress in Acidic Conditions

Ornprapa Anugoolprasert
a
, Hiroshi Ehara
a,*
, Shina kinoshita
a
, Hitoshi Naito
b
, Somchai
Chakhatrakan
c

a
Graduate School of Bioresources, Mie University, Mie, Japan
b
College of Life Science, Kurashiki University of Science and the Arts, Okayama, Japan
c
Department of Agricultural and Technology, Thammasat University, Pathumthani, Thailand
*Corresponding author: Graduate School of Bioresources, Mie University, 1577 Kurimamachiya-cho, Tsu,
Mie 514-8507, Japan.
Tel.: +81 59 231 9495; fax: +81 59 231 9495.
[email protected]

Abstract

Sago palm (Metroxylon sagu Rottb.) grows in natural peat swamps, which are poorly drained and has high
acidity and generally contain highly exchangeable Al. It is, therefore, considered to be acid- and Al-resistant. In
this study, the growth, physiological characteristics and nutrient concentrations in the plant tissues of sago palm
grown under a hydroponic system were investigated for 4.5 months. When sago palm seedlings were cultured at
pH 5.7, pH 4.5 and pH 3.6, the leaf morphogenesis, nutrient uptake and dry matter production were maintained
regardless of a small decrease in the photosynthetic rate through the decrease of stomatal conductance. In the
case in which seedlings were grown at pH 3.6 with different levels of AlCl
3
6H
2
O corresponding to 0, 10, 20, 100
and 200 ppm Al, the plant length and dry matter production increased with a mild Al concentration in the growth
media, such as 10 ppm Al. This result was attributed to the increase in the P and N uptake. In contrast, all the
growth parameters significantly decreased under the 200 ppm Al treatment. The critical value to inhibit the
growth of sago palm was considered to be around 200 ppm Al in the growth media. In addition, sago palm
maintained a low Al
3+
concentration in all of the plant parts. Therefore, it could be concluded that sago palm has
high resistance to Al with mechanical restriction of the excess Al based on the Al exclusion ability under the acid
condition.

Keywords: acid resistance, aluminum resistance, dry matter growth, photosynthetic rate, stomatal conductance

Introduction

Competition between biofuel production and food production has occurred in recent years
in the context of the current social background regarding the exhaustion of fossil energy and the
growing world population. Various plants are receiving attention as sustainable energy resources for
the production of bioethanol and biodiesel. However, worldwide arable lands are limited. Thus, the
development and/or improvement of new plant resources and their utilization are needed as a
strategy to secure a sufficient amount of biomass for producing foods and biofuel sources (Ehara,
2009).
Sago palm (Metroxylon sagu Rottb.) stores large quantities of starch in its trunk. The total
starch storage in one trunk is approximately 300 kg dry weight (Ehara, 2005). As a staple food,
sago palm continues to be important in parts of Southeast Asia and in areas inhabited by the
Melanesian people (Ehara et al., 2000). The carbohydrate or starch can be further processed into
various basic raw materials for human and animal consumption as well as an industrial energy
source, such as ethanol. In addition, sago palm grows in swampy, alluvial and peaty soils where
almost no other major crops can grow without drainage or soil improvement (Sato et al., 1979; Jong
& Flach, 1995). Nevertheless, the deep peat soils in swampy areas are usually characterized by low
pH values, a deficiency in mineral elements and a high rate of exchangeable Al (Sato et al., 1979).
Some former field studies on the growth of sago palm reported that sago palm grew under acid
th
conditions (Purwanto et al., 2002; Osaki et al., 2003). According to Foy & Fleming (1978), there was
a possitive correlation between Al-resistant plants in nutrient solution and resistance to low pH
conditions. It is, therefore, assumed that sago palm is resistant to acidic pH and Al. However, few
studies have compared the growth characteristics of sago palm at widely different pH levels as well
as the Al-induced changes on sago palm growth. Thus, the objective of the present study was to
compare the physiological features and growth characteristics of young seedlings of sago palm at
different levels of pH and Al concentration under low pH condition in a hydroponic system to
elucidate the acid- and Al-resistance.


Plant materials and treatments
Sago palm fruits were collected in the swampy areas of Rattapum, Songkhla, Thailand, on
1 August, 2006. Fertilized and well-developed fruits were selected and treated physically to remove
seed coat tissues. The cleaned seeds were placed in a plastic tray filled with tap water and then put
them in a dark temperature-controlled room at 30C in Thammasat University, Thailand. The
germinated seeds were brought to Mie University, Japan and each of them was transplanted to a
1/5000a Wagner pot filled with vermiculite and Kimura B culture solution containing (M) 36.5
(NH
4
)
2
SO
4
, 9.1 K
2
SO
4
, 54.7 MgSO
4
, 18.3 KNO
3
, 36.5 Ca (NO
3
)
2
, 18.2 KH
2
PO
4
and 3.9 FeO
3
(Baba
& Takahashi, 1958). The initial pH of the culture solution was adjusted to 5.5 using 1.0N HCl before
irrigation into pots. The pots were placed in a greenhouse under natural sunlight and maintained at
over 15C, even at night, at Mie University. Daily additions were made to the culture solution,
according to the amount of solution consumed, and the culture solution was renewed twice weekly.
In Experiment 1, three seedlings at the 7
th
leaf stage, with the mean plant length of all plant
material at 39 cm, were selected and treated with Kimura B culture solution at three different levels
of pH, 5.7, 4.5 and 3.6. In Experiment 2, three seedlings of the same size as those in Experiment 1
were treated with Kimura B culture solution without Al (referred to as control hereafter) or containing
different levels of AlCl
3
6H
2
O corresponding to 10, 20, 100 and 200 ppm Al at pH 3.6. The pH of the
culture solution was adjusted with 1.0N HCl as required. The pots were placed in the same
greenhouse under natural sunlight. An air pump was connected to the pots to provide air to the
roots. The culture solutions in each pH and Al treatment were supplemented and renewed every
other day from 23 May to 9 October, 2007.

Photosynthetic rate, transpiration rate, and stomatal conductance
The leaflets of the most active leaves or the 4
th
leaf position from the top of the treated
plants (18 weeks after the treatments) were selected for measuring the net photosynthetic rate,
transpiration rate, and stomatal conductance using a potable photosynthetic meter (Analytical
Development Co., Ltd., LCA-4, England) at saturation irradiance with incident photosynthetically
active radiation (PAR) of 800-1,000 mol m
-2
s
-1
.

Sampling and nutrient concentrations in plants
The treated plants were separated into three parts: leaflets, petioles including rachis, and
roots. The leaflet areas were measured using an automatic area meter (Hayashi-Denko AAM-9,
Japan). The separated samples were dried in an oven at 80C for 72 h to measure the dry weight
and then ground into powder in order to analyze the ion concentrations. The ground samples were
reduced to ash in a furnace and extracted with 1.0N HNO
3
, and the K
+
, Ca
2+
and Mg
2+

concentrations were determined using a high-performance liquid chromatography (HPLC) method
with a conductivity detector (Shimadzu CDD-6A, IC-C3, Japan). The concentration of P was
evaluated by atomic absorption spectrophotometry. The total N concentration was determined by
th
the semi-micro Kjeldahl method, while the Al
3+
concentration was determined calorimetrically by the
aluminon method.
The statistical difference of the data was determined using NCSS 2001 (Number Cruncher
Statistical Systems). The effects of treatments were determined by one-way ANOVA (analysis of
variance), and the differences among the mean values of treatment were determined using the
Tukey-Kramer test.


During the experiment, approximately 7 leaves emerged in each pH treatment. The
number of dead leaves during the experiment was 4, 4 and 3 at pH 5.7, 4.5 and 3.6, respectively.
There were no significant differences in the number of emerged, dead and living green leaves
among the three pH treatments, which means that the low pH conditions had no effect on new leaf
emergence and senescence. Plant growth in weekly increment of length and total leaflet area did
not change with the pH treatments. Although there was no significant difference in the total dry
weight per plant among the pH treatments, the total dry weight in the pH 3.6 treatment was 8.7%
smaller than that in the pH 5.7 treatment (Table 1). Similarly, the photosynthetic rate in the pH 3.6
treatment was 8.3% smaller than that in the pH 5.7 treatment. The difference in photosynthetic rates
among the three pH treatments could be attributed to differences in the stomatal conductance; the
stomatal conductance in the pH 3.6 treatment was 7.5% smaller than that in the pH 5.7 treatment.

Under the Al treatments, the total dry weight and total leaflet area in the 10 ppm Al
treatment were slightly larger than those in the other treatments, while those in the 200 ppm Al
treatment were significantly smaller than those in the control treatment (Table 2). Moreover, the
roots of sago palm seedlings under the 200 ppm Al treatment were stunted, brownish and thick, and
the root dry weight was 58% smaller than that in the control treatment, representing a significant
difference (Table 2). Consequently, the critical value to inhibit the growth of sago palm was
considered to be approximately 200 ppm Al in the growth media, which is much higher than the real
concentrations in the natural soil conditions.
The concentrations of Al
3+
, N, P, K
+
, Ca
2+
and Mg
2+
in the leaflets, petioles, roots and
whole plants under the Al treatments are shown in Table 3. The Al
3+
concentration in all the plant
parts increased with the rise of the Al concentrations. Moreover, the Al
3+
concentration in the leaflet
was lower than that in the petiole and tended to be significantly higher in the root than in the top
parts (leaflets and petiole) in all the Al treatments. Our current results in sago palm strongly support
the assumption that Al
3+
has a high binding ability with cellular components of the root and usually
shows slight translocation to the upper parts of the plant (Ma et al., 1997). The total N and P
concentrations in the whole plants of the 10 ppm Al-treated plant were higher than those in the
control and other Al-treated plants, which could lead to an increase in the growth of sago palm
under a mild Al concentration in the growth media. These results indicated that Al was unlikely to
have induced the P and N deficiency in plant tissues but the uptake of these nutrients was higher
Table 1. Effect of low pH on weekly increment of plant length, leaflet area per plant and dry matter weight
(Experiment 1)

pH
Treatment
Weekly increment
of plant length (cm)
Leaflet area
per plant (cm
2
)
Dry matter weight per plant (g)
Leaflet Petiole Root Whole
pH 5.7
pH 4.5
pH 3.6
2.0 a
2.0 a
2.0 a
2400.6 a
2457.2 a
2418.8 a
18.2 a
19.5 a
17.3 a
23.7 a
22.0 a
20.1 a
8.9 a
10.8 a
9.0 a
50.8 a
52.3 a
46.4 a
Means with the same letters in a given column are not significantly different at the 0.05 level by the Tukey-
Kramer test (n=3).

th
under a lower Al condition, as such evidence was also found in rice (Fageria, 1985) and some
native plants (Osaki et al., 1997). The K
+
concentration in all the plant parts was independent of the
Al treatment. Whereas the Ca
2+
and Mg
2+
concentrations in whole plants decreased by the increase
of the Al concentrations in the growth media, a significant difference was clearly observed in the
200 ppm Al-treated plants. One interesting feature of these results is that Al
3+
inhibited Ca
2+
and
Mg
2+
absorption more than K
+
absorption in all the plant parts under the higher Al treatment. The
possible mechanism to explain the different effects on cations is that the Al
3+
toxicity was
ameliorated by cations in the following order, H
+
approximately = C
3+
> C
2+
> C
+
, and the
amelioration was due to their binding to or screening the negative charges on the plasma
membrane (Kinraide et al.,1992).

According to Chenery (1948), thousands of the plant species are classified, according to
their Al concentrations in plant tissues, as Al-accumulators ( 1,000 mg Al kg
-1
dry weight) or Al
excluders (< 1,000 mg Al kg
-1
dry weight). Some plant species known as the Al accumulators may
contain more than 10 times this Al level without any Al injury. However, most plants contain no more
than 300 mg Al kg
-1
dry weight. In the current study, the range of Al
3+
concentrations in whole plants
of sago palm was from 9.4 to 15.6 mol g
-1
(254 to 420 mg kg
-1
) dry weight even under the 200 ppm
Al treatment (Table 3). Considering the result of the Al
3+
concentration in whole plant tissues, sago
palm is considered to have high resistance to Al with mechanical restriction of the excess Al based
on its Al exclusion ability under acid conditions.
Table 2. Effect of Al concentration on weekly increment of plant length, leaflet area per plant and dry matter
weight (Experiment 2)

Al
concentration
(ppm)
Weekly increment
of plant length (cm)
Leaflet area
per plant
(cm
2
)
Dry matter weight per plant (g)
Leaflet Petiole Root Whole
Control
10
20
100
200
2.0 a
2.0 a
1.9 ab
1.9 ab
1.7 b
2418.8 ab
3008.6 a
2092.0 b
2151.7 b
1153.4 c
17.3 ab
23.0 a
15.7 bc
15.1 bc
8.0 c
20.1 ab
27.1 a
16.3 b
18.0 b
11.2 c
9.0 ab
13.6 a
6.7 b
6.6 b
3.8 c
46.4 ab
63.7 a
38.7 bc
39.7 bc
22.9 c
Means followed by different letters within a column are significantly different at the 0.05 level by the Tukey-
Kramer test (n=3).

th

References

Baba I and Y Takahashi. 1958. Solution culture. In Y. Togari ed., Sakumotsu Shiken Ho. Nogyo Gijutsu Kyokai,
Tokyo. 327-343.
Chenery EM. 1948. Aluminium in the plant world: I. General survey in dicotyledons. Kew Bull. 2: 173-183.
Ehara H, S Susanto, C Mizota, S Hirose and T Matsuno. 2000. Sago palm (Metroxylon sagu, Arecaceae)
production in the eastern archipelago of Indonesia: Variation in morphological characteristics and pith-
dry matter yield. Econ. Bot. 54: 197-206.
Ehara H. 2005. Geographical distribution and specification of Metroxylon palms. Jap. J. Trop. Agr. 49: 111-116.
Ehara H. 2009. Potency of sago palm as carbohydrate resource for strengthening food security program. J.
Agron. Indonesia 37: 209-219.
Fageria NK. 1985. Influence of aluminum in nutrient solutions on chemical composition in two rice cultivars at
different growth stages. Plant Soil 85: 423-429.
Foy CD and AL Fleming. 1978. The physiology of plant tolerance to excess available aluminum and manganese
in acid soils. ASA spec. 32: 301-328.
Jong FS and M Flach. 1995. The sustainability of sago palm (Metroxylon sagu) cultivation on deep peat in
Sarawak. Sago palm 3: 13-20.
Kinraide TB, PR Ryan, and LV Kochian. 1992. Interactive effects of A1
3+
, H
+
, and other cations on root
elongation considered in terms of cell-surface electrical potential. Plant Physiol. 99: 1461-1468.
Ma JF, SJ Zheng, H Matsumoto and S Hiradate. 1997. Detoxifying aluminum with buckwheat. Nature 390: 569-
570.
Osaki M, T Watanabe and T Tadano. 1997. Beneficial effect of aluminum on growth of plants adapted to low pH
soils. Soil Sci. Plant Nutr. 43: 551-563.
Table 3. Effect of Al concentration on nutrient concentrations in the leaflets, petioles, roots and whole plants
(Experiment 2)

Nutrient
concentration
Plant
part
Al concentration (ppm)
Control 10 20 100 200
Al
3+
(mol g
-1
) Leaflet 8.7 cB 9.5 bcB 10.3 bB 10.2 bcB 14.3 aB
Petiole 8.9 bB 10.7 abB 11.6 abB 13.1 abB 15.1 aB
Root 12.1 cA 15.1 bcA 16.3 abA 17.7 abA 19.8 aA
Whole 9.4 b 11.2 b 11.9 ab 12.7 ab 15.6 a
N (mg g
-1
) Leaflet 20.9 aA 24.6 aA 23.0 aA 22.6 aA 21.0 aA
Petiole 8.8 aB 9.1 aB 8.7 aB 7.7 aB 6.3 aB
Root 10.8 aB 9.9 aB 9.8 aB 10.2 aB 11.3 aAB
Whole 13.6 a 14.8 a 14.6 a 14.1 a 12.6 a
P (mg g
-1
) Leaflet 1.8 aA 1.9 aA 1.8 aAB 1.7 aAB 1.6 aAB
Petiole 2.2 aA 2.3 aA 2.2 aA 1.9 aA 1.4 bA
Root 1.6 abA 1.8 aA 1.4 abB 1.1 bcB 0.9 cB
Whole 1.9 ab 2.0 a 1.9 ab 1.7 ab 1.4 b
K
+
(mol g
-1
) Leaflet 93.5 aB 92.6 aB 97.8 aB 93.4 aB 98.5 aB
Petiole 219.6 bA 199.5 bA 215.4 bA 220.0 bA 250.7 aA
Root 253.4 aA 209.3 bA 226.7 abA 250.7 aA 267.0 aA
Whole 178.2 b 162.8 b 170.7 b 173.9 b 200.0 a
Ca
2+
(mol g
-1
) Leaflet 42.4 aB 45.3 aB 42.6 aB 32.8 abB 25.5 bA
Petiole 55.7 abA 64.4 aA 65.2 aA 47.7 bA 28.9 cA
Root 28.8 abB 36.1 aB 36.8 aB 30.5 abB 21.7 bA
Whole 45.7 ab 51.4 a 51.3 a 39.2 b 26.7 c
Mg
2+
(mol g
-1
) Leaflet 41.1 aB 40.3 aB 40.9 aB 34.8 abC 29.0 bA
Petiole 56.7 abAB 60.4 aA 63.0 aA 46.6 bB 29.5 cA
Root 63.9 aA 65.1 aA 67.4 aA 66.8 aA 36.2 bA
Whole 52.1 ab 54.1 a 55.1 a 45.5 b 30.5 c
Means followed by different letters within a row are significantly different at the 0.05 level by the Tukey-Kramer test (n=3).
Lowercase letters indicate a comparison among the Al treatments in each part of a plant. Capital letters indicate a
comparison among plant tissues under the various Al treatments.

th
Osaki M, T Watanabe, T Ishizawa, C Nilnond, T Nuyim, T Shinano, M Urayama and SJ Tuah. 2003. Nutritional
characteristics of the leaves of native plants growing in adverse soils of humid tropical lowlands. Plant
Foods Hum. Nutr. 58: 93-115.
Purwanto BH, K Kakuda, H Ando, JF Shoon, Y Yamamoto, A Watanabe and T Yoshida. 2002. Nutrient
availability and response of sago palm (Metroxylon sagu Rottb.) to controlled release N fertilizer on
coastal lowland peat in the tropics. Soil Sci. Plant Nutr. 48: 529-537.
Sato T, T Yamaguchi and T Takamura. 1979. Cultivation, harvesting and processing of sago palm. Jpn. J. Trop.
Agr. 23: 130-136.

th
Transplanted Sucker Stem Growth in Sago Palm (Metroxylon sagu Rottb.)
Before Trunk Formation

Satoshi Nakamura
a,*
, Keita Nabeya
b
, Mutsumi Akama
b,
, Teiji Nakamura
b
,
Youji Nitta
c
, Manabu Watanabe
d
, Yusuke Goto
b

a
School of Food, Agricultural and Environmental Sciences, Miyagi University, Sendai, Miyagi, Japan
b
Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan
c
College of Agriculture, Ibaraki University, Ami, Ibaraki, Japan
d
Field Science Center, Faculty of Agriculture, Iwate University, Morioka, Iwate, Japan
*Corresponding author: School of Food Agricultural and Environmental Sciences,
2-2-1, Hatatate, Taihaku-ku, Sendai, Miyagi, 982-0215, Japan.
Tel.: +81 22 245 1278; Fax: +81 22 245 1278.
[email protected]

Abstract

Sago palm sucker stems transplanted in fields creep along the ground surface during a rosette stage, later
forming a vertical trunk. Many suckers grow at the stem bottom before trunk formation. Thinning and pruning of
suckers, known as sucker control, is extremely important to maintain an appropriate density of trunks and to
produce much starch in sago plantations over time. Selection of suckers with consideration of the suckers
creeping growth is necessary to determine the appropriate spread of trunks in a field. Nevertheless, few reports
describe the creeping growth of sucker stems. This study was undertaken to clarify the creeping growth of
suckers transplanted in a field under sucker control before trunk formation. Suckers were transplanted in a field
in Mukah, Sarawak, Malaysia on September 3, 2005. The plant density was 330 plants ha
-1
. The growth of 12
suckers was monitored and the sucker stem lengths were measured every year during 20082011. The average
stem lengths were 74.2 4.7 cm and 155.3 6.3 cm, respectively, at 1,201 days and 2,120 days after
transplantation. The length increased linearly at 31.5 cm year
-1
(Y = 0.0862X 25.301, r = 0.993, P < 0.001,
where Y is the stem length and X is the days after transplanting). Each year, 10.5 leaves expanded. Although
sucker growth differs among soil types, regions, and varieties, the information collected in this study is expected
to be useful for predicting the trunk position.

Keywords: creeping growth, sago palm, stem, sucker, sucker control

Introduction

Sago palm sucker stems transplanted in fields creep along the ground surface during a
rosette stage, later forming a vertical trunk. Many suckers grow at the stem bottom before trunk
formation. These suckers derive carbohydrates from the mother palm, the transplanted sucker, until
the photosynthetic apparatus is sufficiently developed and absorbs enough sunlight (Flack, 1977).
Emergence and growth of many suckers at the stem bottom are expected to exacerbate
competition between the suckers and their mother-palm for nutrition from soil because of their
proximity. For that reason, the mother-palm growth might be suppressed. Reportedly, the rate of
leaf emergence of non-controlled suckers is significantly lower than that of controlled suckers during
the first five months of growth (Nakamura et al., 2009). Consequently, thinning and pruning of
suckers, known as sucker control, is extremely important to promote the growth of mother palm, to
maintain an appropriate density of trunks, and to maintain higher starch productivity in sago
plantations over time. Selection of suckers with consideration of the suckers creeping growth is
therefore necessary to determine the appropriate spread of trunks in a field. Nevertheless, few
reports describe the creeping growth of sucker stems. This study was undertaken to clarify the
creeping growth of suckers that had been transplanted in a field, with sucker control applied before
trunk formation.
th

Suckers were transplanted in a field in Mukah (N 025631, E 1121826), Sarawak,
Malaysia on 3 September 2005. The plant density was 330 plants ha
-1
; the plant mean area was
30.5 m
-1
. The growth of 12 suckers was monitored: the sucker stem lengths were measured each
year during 20082011. The transplanted sucker stem length was defined as the distance from its
end to its shoot apex, which was covered with thick leaf sheaths. We were able to monitor their
growth. Therefore, the shoot apex position was estimated from anatomical features of young sago
palms sampled in the same field in 2008 (Figure1). The leaves of suckers were marked for
monitoring using a marker pen. The number of expanded leaves was recorded. The number of their
green leaves was also recorded each year.

Figure 1. Mother palm sampled in the field in 2008 (a) and its stem, from which leaf sheaths were removed (b).
Circles show the estimated position of the shoot apex.


All transplanted suckers grew well during 2005-2011 (Figure 2). The average stem lengths
were 74.2 4.7 cm and 155.3 6.3 cm, respectively, at 1,201 days (17 December 2008) after
transplanting (1,201 DAT) and 2,120 DAT (24 June 2011) (Figure 3), which suggests that the length
increased linearly at 31.5 cm year
-1
(Y = 0.0862X 25.301, r = 0.993, P < 0.001, where Y is the
stem length and X is the DAT). The stem length was observed to increase gradually, probably
increasing exponentially until the start of linearly incremental extension of the stem length (Goto et
al., 2010). Because some suckers that start trunk formation were observed at 1,201 DAT, the rate
of creeping growth of sucker is expected to decrease. The final stem length is reached soon
thereafter.

Figure 2. Mother palm, of which the stem has been creeping, at 2,120 days (in 2011) after transplantation.

a
)
b
)
th
0
50
100
150
200
0 500 1,000 1,500 2,000 2,500
S
t
e
m

l
e
n
g
t
h

(
c
m
)
Days after transplanting (DAT)

Figure 3. Stem length of the sucker after transplanting. Vertical bars represent standard errors.

The average numbers of living leaves of the suckers were 16.0 0.6 and 11.2 0.5,
respectively, at 1,201 DAT and 2,120 DAT (Figure 4). The green leaf number tended to decrease,
although the total and each area of leaves increased. It was observed that the size of leaves and
the number of leaflets at 2,120 DAT was greater than those at 1,201 DAT. Results of leaf position
data showed that 26.5 new leaves expanded from 1,201 DAT to 2,120 DAT, suggesting that 10.5
leaves expanded each year.

5
10
15
20
0 500 1,000 1,500 2,000 2,500
N
u
m
b
e
r

o
f

g
r
e
e
n

l
e
a
v
e
s
Days after transplanting (DAT)

Figure 4. Number of green leaves of the sucker after transplanting. Vertical bars represent standard errors.

Conclusions

In conclusion, the rate of creeping growth of sucker stem in a field was specified after
transplantation by monitoring the stem length. Although sucker growth is expected to differ among
soil types, regions, and varieties, the information collected in this study will be useful for predicting
the trunk position in a field.

Acknowledgements
This work was supported by KAKENHI 20405017. We are also grateful to Mr. Smith in Mukah,
Malaysia for their kind assistance.

y = 0.0862X 25.301
r = 0.993***
th
References

Flack, M. 1977. Yield potential of the sago palm and its realization. In M.A. Tankooling ed., Sago 76: Papers of
the First International Sago Symposium, Kuala Lumpur. 157-177.
Goto, Y., Nakamura, S., Nakamura, T., Nitta, Y. and Watanabe M. 2010. The sucker-control and the creeping
growth of sago palm (Metroxylon sagu Rottb.). Jpn. J. Crop Sci. 61 (Extra issue 1): 220-221. (in
Japanese).
Nakamura, S., Nitta, Y., Watanabe, M., Nakamura, T. and Goto, Y. 2009. Effect of sucker control on the leaf
emergence of sago palm (Metroxylon sagu Rottb.) before trunk formation. Jpn. J. Crop Sci. 60 (Extra
issue 1): 260-261. (in Japanese).

th
Secondary Aerenchyma Formation and Root Growth Response of Soybean
(Glycine max) Seedlings under Flooded Conditions

Toshihiro Mochizuki
a,
*, Satomi Sakazono
b
, Sayuri Kajihara
c
,
Satoshi Shimamura
d

a
Faculty of Agriculture, Kyushu University, Fukuoka, Japan
b
Graduate School of Life Sciences, Tohoku University, Miyagi, Japan,
c
School of Agriculture, Kyushu University,
d
National Agricultural Research Center for Tohoku Region, Akita, Japan
* Corresponding author: Experimental Farm, Kyushu University, Harumachi 111, Kasuya-machi, Kasuya-gun,
Fukuoka 811-2307, Japan
Tel.: +81 92 612 2865; fax: +81 92 612 2865.
[email protected]

Abstract

Most of wetland species can develop their roots into flooded soils because of the presence of
longitudinal aerenchyma channels that facilitates oxygen diffusion from shoot to root tips. This
tissue is called as primary aerenchyma because it is formed in fundamental tissues. It is also
formed in rice root, consequently rice plants can grow well in paddy field. On the other hand, it is
considered that most of mesophytes such as field crops cannot grow under flooded and excess
moisture conditions because of their low ability to develop aerenchyma. However, we found that
soybean plants could develop aerenchyma and grow well in flooding compared with other
leguminous crops such as Vigna and Phaseolus species. This type of aerenchyma, which is
consisted of white spongy tissue filled with gas space and is differentiated from secondary meristem
(phellogen), is called assecondary aerenchyma. It plays a role in supplying oxygen from the aerial
parts to the flooded roots and nodules. In our recent study, it was observed that there was a wide
range of varietal differences on secondary aerenchyma formation and adventitious root
development in soybean seedlings under flooding. Although the research for secondary
aerenchyma in soybean plants is on the way, it may be able to breed soybean varieties with
flooding tolerance.

Keywords: anaerobiosys, flooding, secondary aerenchyma, soybean, water logging

Introduction

Flooding is a major problem in many areas of the world and most of mesophytes such as
field crops are susceptible to the stress. Therefore, an understanding of the morphological
mechanisms of flooding tolerance is important for developing flood-tolerant genotypes. Aerenchyma
formation is one of the morphological changes that occurs in plants grown under flooded and
hypoxic conditions and it is thought to enhance the internal diffusion of atmospheric and
photosynthetic oxygen from the aerial parts to the flooded roots, allowing the roots to maintain
aerobic respiration (Armstrong, 1979). The two types of aerenchyma are classified. One is cortical
(lysigenous or schizogenous) aerenchyma formed in the roots of rice, maize, barley, wheat and
some Rumex species. The other is white spongy tissue filled with gas spaces and is formed in the
stem, hypocotyl, tap root, adventitious roots and root nodules of Glycine soja, Sesbania rostrata,
Lotus uliginosus and Viminaria juncea grown under flooded conditions. It is differentiated from
secondary meristem (phellogen) and is called secondary aerenchyma (Jackson and Armstrong,
1999). Secondary aerenchyma seems to play a role in supplying oxygen to roots and nodules. In
th
contrast to cortical aerenchyma, however, there is little information about the morphological and
anatomical processes of secondary aerenchyma formation and its function.
Soybean is generally susceptible to flooding, and its growth and yield are negatively
affected by the stress. Arikado (1954) suggested that soybean had low flooding tolerance because
of its low ability to develop aerenchyma in the shoot and roots. However, some soybean genotypes
can form lysigenous aerenchyma in the root cortex (Bacanamwo and Purcell, 1999) and secondary
aerenchyma in the hypocotyl and tap root of seedlings grow under flooded conditions (Mochizuki et
al., 2000). In this paper, we introduced our recent studies of the morphological and anatomical
processes of secondary aerenchyma formation and its function as an oxygen pathway from the
aerial parts to flooded roots, and we described here the relationship between aerenchyma formation
and the flooding tolerance of soybean.

Secondary aerenchyma formation in flooded soybean

We investigated secondary aerenchyma formation in soybean seedlings grown under
flooded conditions (Shimamura et al., 2003). As a result, within 3 weeks of flooding, large volumes
of secondary aerenchyma developed in flooded hypocotyl, tap root, adventitious roots and nodules
(Fig. 1). This tissue has large intercellular spaces and consists of living cells whose walls do not
become suberized, whereas phellem has no intercellular spaces and consists of dead cells whose
walls become suberized. It is differentiated from secondary meristem (phellogen) and is
homologous with cork tissue (Fig. 2). Cells were exposed to the outside through lenticels in
hypocotyl and roots where epidermis and cortex layers were collapsing. The outer part of the
nodules was covered with a layer of secondary aerenchyma that was relatively thinner in the
nodules than in the hypocotyl and roots. Nodules attached to the face of roots had pink infected
tissues, which suggested the presence of leghemoglobin and the survival of nodules under flooded
conditions.
.
a, root system; b, transverse section of an adventitious root; c, transverse section of a nodule. WL, water level; SS, soil surface;
AR, adventitious roots; RN, root nodules; SA, secondary aerenchyma.

Figure 1. Root system and secondary aerenchyma development in soybean seedlings after 3 weeks of flooding.
th

Figure 2. Cross sections of young hypocotyl in soybean.

Function of secondary aerenchyma in flooded soybean

Oxygen dynamics in aerenchymatous stems were investigated using Clark-type O
2

microelectrodes, and O
2
transport to roots was evaluated using stable-isotope
18
O
2
as a tracer, for
plants with shoots in air and roots in flooded sand or soil (Shimamura et al., 2010).
After introducing
18
O
2
gas via the stem lenticels, significant
18
O
2
enrichment in water
extracted from roots after 3 h was confirmed, suggesting that transported O
2
sustained root
respiration. In contrast, slight
18
O
2
enrichment was detected 3 h after treatment of stems that lacked
aerenchyma and lenticels. The results showed that hypertrophic lenticels in the lower stem of
soybean, just above the water surface, are entry points for O
2
, and these connect to aerenchyma
and enable O
2
transport into roots in flooded soil.

Flood Ae-Open, aerenchyma and lenticels above the water; Flood Ae-Submerged, submerged aerenchyma and lenticeles.
Values are the mean s.e. Means in the shoot followed by the same upper-case letter and means in the root followed by the
same lower-case letter do not differ significantly (P<0.01, Tukey-Kramers test).

Figure 3. Volume of
18
O
2
transported from the stem to the roots with or without exposure of the aerenchyma to
the
18
O
2
gas in each treatment.

th
Interspecific difference in secondary aerenchyma formation of flooded leguminous crops

We investigated the secondary aerenchyma formation in hypocotyls just below the soil
surface of young seedlings in wild soybean and six summer leguminous crops grown under upland
and flooded conditions for 14 days (Mochizuki et al., 2000).
Under the upland conditions, secondary aerenchyma was scarcely observed in any
species. Under the flooded conditions, however, there was an interspecific difference in the
secondary aerenchyma formation. Secondary aerenchyma area per transverse section of
hypocotyls under the flooded conditions was largest in soybean Asoaogari; followed by soybean
Akisengoku, wild soybean D5, cowpea Sanjakusasage, mung bean Bundomame, and mung
bean Acc. 7703, and those in the other crops were less than 1 mm
2
(Table 1). Since a significant
positive correlation was found between dry weight ratio (the ratio of dry weight of the aerial part
under the flooded conditions to that under the upland conditions) and secondary aerenchyma area
(r=0.738*), it is suggested that the ability of secondary aerenchyma formation is related to the
flooding tolerance in leguminous crops.

Table 1. Secondary aerenchyma area of hypocotyl and dry weight ratio in summer leguminous crops

Secondary aerenchyma ratio is the percentage of secondary aerenchyma area to steal area. Dry weight ratio is the percentage
of dry weight of the aerial part under flooded conditions to that under upland conditions. Values followed by the same letter in
each column are not significantly different at P<0.05 by Duncan's multiple test.

Effects of hypoxia on dry matter production and root development in soybean and wild
soybean cultivars

Using 91 soybean and wild soybean cultivars, effects of hypoxia on dry matter production
and root development were examined (Sakazono et al., 2011). Seedlings of eight days after sowing
were grown in solution culture with (control) and without (hypoxia) O
2
. Seven days after treatment,
dry weight, root characters and hypocotyl diameter were measured. Root characters were
measured with Win RHZO (Regent Instruments Inc., Quebec, Canada). In this experiment, we use
the ratio of hypocotyl diameter (ratio of hypocotyl diameter in hypoxia to that of control) as an
indicator of secondary aerenchyma development in hypoxia.
Effect of hypoxia was higher in root growth than shoot growth. Total root length, root
surface area and root volume were decreased by hypoxia, whereas average root diameter and
th
hypocotyl diameter were increased. However, in every trait including hypocotyl diameter, there was
wide variation among cultivars.

Table 2. Effects of hypoxia on dry matter production and root development in soybean and wild soybean
cultivars

Conclusions

It is clearly that the secondary aerenchyma formed in soybean plays a role in supplying
oxygen from aerial parts to roots and nodules, and there are interspecific and intraspecific
differences in the secondary aerenchyma formation. Although the research for secondary
aerenchyma in soybean plants is on the way, it may be able to breed soybean varieties with
flooding tolerance.

References

Arikado H. 1954. Different responses of soybean plants to an excess of water with special reference to
anatomical observations. Proc. Crop Sci. Soc. Japan 23:2836.
Armstrong W. 1979. Aeration in higher plants. Adv. Bot. Res. 7:225332.
Bacanamwo M., L.C. Purcell. 1999. Soybean root morphological and anatomical traits associated with
acclimation to flooding. Crop Sci. 39:143149.
Jackson M. B., W Armstrong. 1999. Formation of aerenchyma and the processes of plant ventilation in relation
to soil flooding and submergence. Plant Biol. 1:274287.
Mochizuki T, U Takahashi, S Shimamura and M Fukuyama. 2000. Secondary aerenchyma in hypocotyl in
summer leguminous crops. Jpn. J. Crop Sci. 69:69-73. (In Japanese with English abstract).
Sakazono S, R Matsuo, S Kajihar, M Ishimoto, K Harada, R Takahashi and T Mochizuki. 2011. Flooding
tolerance variation among soybean cultivars and lines at cotyledon stage. Jpn. J. Crop Sci. 80 (special
issue 1):442-443. (In Japanese).
th
Shimamura S, T Mochizuki, Y Nada and M Fukuyama. 2003. Formation and function of secondary aerenchyma
in hypocotil, roots and nodules of soybean (Glycine max) under flooded conditions. Plant and Soil 251:351-
359
Shimamura S, R. Yamamoto, T Nakamura, S Shimada and S Komatsu. 2010. Stem hypertrophic lenticels and
secondary aerenchyma enable oxygen transport to roots of soybean in flooded soil. Ann. Bot. 106:277-
284.

th
Agronomical Performances of Soybean Cultivated under
Saturated Soil Culture on Tidal Swamps

M. Ghulamahdi
a
, M. Melati
a
, S. A. Aziz
a
, A. Junaedi
a
, Sahuri
a
, Y. Puspitasari
a
,
D. Sagala
b

a
b
Department of Agronomy, Faculty of Agriculture, Prof Azairin University, Bengkulu, Indonesia
* Corresponding author:

Department of Agronomy and Horticulture, Faculty of Agriculture,
Bogor Agricultural University, Kampus IPB, Dramaga, Bogor, Indonesia 16680
Tel/fax : +62-251-8629353
[email protected]

Abstract

Saturated soil culture (SSC) is a cultivation technology mantaining water depth constanly to make soil layer in
the saturated condition. This paper resumes of two experiments to evaluate the effect of water depth and bed
width, and leaching time and varieties of soybean cultivated under SSC on tidal swamp. The research was
conducted at Banyu Urip, Banyuasin, South Sumatra from April to August 2010. In the first experiment, water
depth in the furrow irrigation as main-plot consisted of 10 and 20 cm under soil surface (USS) and bed widths as
sub-plot consisted of 2, 4, 6 and 8 m. The results showed that the highest grain yield was obtained on 20 cm
USS water depth and bed width 2 m (4.15 ton/ha), it was significantly different from those at bed width 4 m (2.59
ton/ha), 6 m (1.84 ton/ha) and 8 m (1.74 ton/ha). The grain yield on water depth 10 cm USS and bed width 2 m
obtained was 3.43 ton/ha, it was significantly different from those at bed width 4 m (2.46 ton/ha), 6 m (1.75
ton/ha) and 8 m (1.68 ton/ha). In the second experiment, leaching time as main-plot consisted of without
leaching, every 2, 4 and 6 weeks, and soybean variety as sub-plot consisted of Tanggamus, Slamet, Willis and
Anjasmoro. The results showed that interaction between leaching time and varieties did not significally affect
grain yield, varieties responded leaching time differently. The highest grain yield was obtained by Anjasmoro
variety with leaching time every 2 weeks (4.06 ton/ha) but it was not significally different from those with leaching
time every 4 weeks (3.99 ton/ha) and every 6 weeks (3.93 ton/ha). From these experiments, water depth 20 cm
USS and bed width 2 m may be recommended for SSC soybean cultivation on tidal swamp, and presumably,
leacing time every six weeks will gain more effective economically and technically.

Keywords: leaching time, saturated soil, tidal swamp, water depth, bed width

Introduction

One alternative system to develop soybean cultivation in Indonesia is to optimize the use
of marginal land, and tidal swamp is one of the potential ecosystem for future soybean production.
Indonesia has about 20 million ha tidal swamps, 9 millions ha out of them is appropriate for
agriculture, 2 milions is suitable for soybean (Noor and Sabur, 2007). The major constrain of
producing soybean in tidal swamp due to its high pyrite content. When pyrite is oxidized, soil pH
decreases. Djayusman et al. (2001) reported that high pyrite content suppressed the productivity of
soybean on tidal swamps to only about 800 kg/ha. SSC is a technology in cultivation giving water
permanently, maintains and keeps its depth constantly (about 5 cm USS). This makes soil layer in
saturated condition. In SSC, watering is started from the beginning of growth to maturity stage. By
keeping the water-table constantly, soybean will be avoided from negative effect of inundation on
soybean growth, because soybean will acclimatize and improve its growth (Troedson et al., 1985).
Soil water management can be applied to reduce pyrite content where the soil is in
reductive condition and able to support soybean growth. SSC technology is one of soil water
managements studied in highland and succeed to increase soybean production (Indradewa et al.,
th
2004; Ghulamahdi et al., 2006). This offers the chance to reduce the pyrite, hence increase
soybean production on tidal swamps. Adisarwanto (2001) suggested for soybean cultivation using
bed width less than 2 m. The addition of bed width will reduce the use of labor in the preparing land
to make the trench, but to consider the ability of water seeped from the trench into the middle of
beds. Indradewa et al. (2002) reported that the inundation in the trench with 3-4 m wide bed was the
ideal plot. There was no difference in the influence of bed width on the growth and yield of soybean.
Response of soybean to saturated condition varied between varieties and the later-maturing
soybean was better than the earlier one (CSIRO, 1983; Ghulamahdi et al., 1991; Ghulamahdi,
2008; Ghulamahdi and Nirmala, 2008). Many varieties of soybean have been studied in their
response on acid soil. Alihamsyah and Ar-Riza (2006) found that Tanggamus, Wilis and Slamet
were varieties that could adapt well on inland. Leaching of land can decrease negative effect of
poisonous material (Fe, Al, Mn) to the soybean growth. The frequency of water drainage from the
trench will effect to the content of poisonous material. The objectives of the research were : 1) to
study the effect of water depth and bed width , and 2) to investigate the effect of leaching time and
varieties to the growth and production of soybean under SSC on tidal swamps.


This research was conducted on tidal swamps land in Banyuurip Village of Tanjung Lago
Sub District, Banyuasin District, South Sumatera, Indonesia from April to August 2010. In the first
experiment, water depth in the furrow irrigation as main-plot consisted of 10 and 20 cm under soil
surface (USS) and bed widths as sub-plot consisted of 2, 4, 6 and 8 m. This experiment used
Tanggamus variety. In the second experiment, leaching time as main-plot consisted without
leaching, every 2, 4 and 6 weeks, and soybean variety as sub-plot consisted of Tanggamus,
Slamet, Willis and Anjasmoro. Each main plot was surrounded by furrow irrigation. Water was given
at planting time and kept until the maturity stage and made plots in wet condition. Two weeks before
planting, plots were applied with 2 ton dolomite/ha, 400 kg SP18/ha, and 100 kg KCl/ha. Soybeans
were sprayed with 10 g Urea/l water at 2, 4, 6 weeks after planting to support acclimatization.
At planting date, seeds were inoculated with Rhizobium sp and treated with insecticide with
active agent Carbosulphan 25.53%. Seeds were planted in 2 x 5 m plot size, 20 x 25 cm planting
distance, 2 seeds per hole. The observed variables were : nodule, root, stalk, and leaves dry weight
at 6 weeks after planting (WAP); plant height, number of branch, fill pod, and empty pod per plant,
seed productivity (ton/ha), and 100-seed dry weight at harvest time.


In the first experiment, there was the influence of water depth on the leaf, stalk, root and
nodule dry weight at 6 WAP. The leaf, stalk, root and nodule dry weight were significantly higher in
the water depth 20 cm USS than that ini 10 cm USS (Table 1). This was predicted because the root
growing zone in the water depth 20 cm USS wider than 10 cm USS, so it provied adequate for
maximum root growth. According to Suwarto et al. (1994) water depth significantly influenced on the
leaf, stalk, root and nodule dry weight.
Water depth affected the plant height, number of branch and fill pod per plant, but there
was no influence of water depth on the number of empty pod and 100 seed weight. Plant height,
number of branch and fill pod and productivity of soybean were significantly higher in the water
depth 20 cm USS than those in 10 cm USS (Table 2).

th
Table 1. The effect of water depth on leaf, stalk, root, and nodule dry weight at 6 WAP

Water Depth (cm) Leave (g) Stalk (g) Root (g) Nodule (g)
10 3.52b 3.64b 0.73b 0.33b
20 4.51a 4,84a 0.99a 0.48a
Note: numbers followed by the same letter on the same column are not significantly different with Duncan multiple range test at 5%.

Table 2. The effect of water depth on plant height, number of branch and fill pod, and productivity at harvest time

Water Depth
(cm)
Plant Height
(cm)
Branch/Plant Fill Pod/Plant
Productivity
(ton/ha)
10 70.66b 4.22b 67.83b 2.33b
20 73.86a 4.55a 71.83a 2.58a
Note: numbers followed by the same letter on the same column are not significantly different with Duncan multiple range test at 5%.

There was the influence of bed width on the leaf, stalk, root and nodule dry weight. The leaf,
stalk, root and nodule dry weight were significantly higher in the bed width 2 m than that with the
other bed widths (Table 3). This was predicted because the water seepage from the ditch into the
middle of bed highest distributed on the bed width 2 m.

Table 3. The effect of bed width on leaf, stalk, root, and nodule dry weight at 6 WAP

Variables Bed Width 2 m Bed Width 4 m Bed Width 6m Bed Width 8m
Leave dry weight (g) 4.57a 4.29ab 4.03ab 3.17b
Stalk dry weight (g) 5.27a 4.48ab 4.09ab 3.11b
Root dry weight (g) 1.09a 0.83ab 0.78ab 0.72b
Nodule dry weight (g) 0.58a 0.40b 0.34cb 0.29c
Note: numbers followed by the same letter on the same line are not significantly different with Duncan multiple range test at 5%.

At harvest time, there was the influence of bed width on the number of branch, fill pod per
plant, seed productivity, and 100 seed weight, but there was no influence on the plant height and
empty pod. Number of branch, fill pod, seed productivity, and 100 seed weight were significantly
higher in bed width 2 m than those in the other bed widths (Table 4). Indradewa et al. (2002)
concluded that there was no difference in the effect of bed width on soybean growth and yield.

Table 4. The effect of bed width on number of branch and fill pod, productivity and 100 seed weight at harvest time

Variables Bed Width 2 m Bed Width 4 m Bed Width 6 m Bed Width 8 m
Branch/plant 4.71a 4.41ab 4.33ab 4.05b
Fill Pod/plant 80.17a 73.50b 65.17c 60.17d
Productivity (tones / ha)
3.79a 2.52b 1.79c 1.71d
100 seeds weight (g) 11.89a 11.30ab 10.98b 10.96b

There was the influence of water depth and bed width interaction on the leaf, stalk, root
and nodule dry weight. The leaf, stalk, root and nodule dry weight were significantly higher in the
water depth 20 cm USS with bed width 2 m than those in the other treatments (Table 5).
At harvest time there was the influence of water depth and bed width interaction on the the
plant height, number of branch, fill pod, seed productivity and 100 seed weight of soybean. There
was no interaction effect of water depth and bed width interaction on the number of empty pods.
Plant height, number of branch and fill pod, seed productivity and 100 seed weight were
significantly higher in the water depth 20 cm USS with bed width 2 m than those in the other
treatments (Table 6).
th
Table 5. The effect of interaction of water depth and bed width on leaf, stalk, root, and nodule dry weight at 6 WAP

Variables
Water Depth (cm) x Bed Width (m)
10x2 10x4 10x6 10x8 20x2 20x4 20x6 20x8
Leaf dry weight (g) 3,22bc 3,68bc 4,14bc 3,90b 5,92a 4,91ab 3,92bc 3,29bc
Stalk dry weight (g) 3,58bc 3,79bc 4,16bc 3,06c 6.96a 5,17ab 4,02bc 3,19bc
Root dry weight (g) 0,69b 0,71b 0,84b 0,65b 1,50a 0,94b 0,72b 0,82b
Nodule dry weight (g) 0,34bc 0,44b 0,30cd 0,22d 0,82a 0,37bc 0,37bc 0,36bc

Table 6. The effect of interaction of water depth and bed width on plant height, number of branch and fill pod,
productivity, 100 seed weight at harvest time

Variables
Water Depth (cm) x Bed Width (m)
10x2 10x4 10x6 10x8 20x2 20x4 20x6 20x8
Plant Height 73,55ab 72,83ab 68,06b 67,65b 77,70a 77,23a 71,14a 70,23b
Branch/plant 4.30ab 4.31ab 4.25ab 3.90b 4.68a 4.48ab 4.41ab 4.18ab
Productivity (tonnes/ha) 3.43b 2.46d 1.75f 1.68g 4.15a 2.59c 1.84e 1.74f

In the second experiment, the leaching time did not affect the variables growth, yield
component, and yield of soybean dry, but that only affected the nodule dry weight. The leaching
time every 2 weeks gave the nodule dry weight per plant significantly different with that at every 4
and 6 weeks, but did not different with without leaching (Table 7).

Table 7. The Effect of leaching time on leaf, stalk, root, and nodule dry weight at 6 WAP

Without Every 2 Weeks Every 4 weeks Every 6 weeks
Nodule dry weight (g) 0.18ab 0.19a 0.11b 0.13b

The variety affected the root, stalk dry weight, and seed productivity, but did not affect the
other variables (Table 8). Stalk and root dry weight of Slamet were highest than those of the other
varieties. The highest of seed productivity was obtained on Anjasmoro (Table 8).

Table 8. The Effect of variety on leaf, stalk, root, and nodule dry weight at 6 WAP

Variables Tanggamus Slamet Wilis Anjasmoro
Stalk dry weight (g) 4.86ab 5.60a 4.07b 3.85b
Root dry weight (g) 0.77ab 0.87a 0.69ab 0.63b
Productivity (ton/ha) 2.73b 2.39b 2.48b 3.83a

The leaching time and variety interaction did not affect the seed productivity (Table 9). The
highest grain yield was obtained by Anjasmoro variety with leaching time every two weeks (4.06
ton/ha), but it was not significally different from those with leaching time every four weeks (3.99
ton/ha) and every six weeks (3.93 ton/ha). This suggested that the leaching time every 6 weeks
gained more effective economically and technically. This productivity of Tanggamus in 2010 was
lower than 2009 (Ghulamahdi, 2009). It was predicted that the Tanggamus was more responsive to
the higher solar radiation than lower solar radiation. The dry climate was in 2009, and wet climate
was in 2010. Based on visualization observation in the field the size of leaf of Tanggamus in dry
th
climate was wider than that in wet climate. Irwan (2006) stated that at high temperatures and low
humidity, solar radiation stimulated the emergence of flower buds into flowers.

Table 9. The effect of interaction on leaching time and variety on the seed productivity (ton/ha)

Leaching Time Tanggamus Slamet Willis Anjasmoro
Without 2.31 2.16 2.44 3.36
Every 2 weeks 3.08 2.41 2.46 4.06
Every 4 weeks 2.80 2.62 2.71 3.99
Every 6 weeks 2.73 2.40 2.29 3.93
Note: numbers followed without letter are not significantly different with Duncan multiple range test at 5%.

References

Adisarwanto, T. 2001. Bertanam kedelai di tanah jenuh air. Bul. Palawija. 1:24-32.
Alihamsyah, T., I. Ar-Riza. 2006. Teknologi pemanfaatan lahan rawa lebak. Hal. 181-201. Dalam D.A.
Suriadikarta, U. Kurnia, H.S. Mamat, W. Hartatik, D. Setyorini (eds). Karakteristik dan Pengelolaan
Lahan Rawa. Ed Ke-. Bogor. Balai Besar Penelitian an Pengembangan Sumberdaya Lahan Pertanian,
Badan Penelitian dan Pengembangan Pertanian, Departemen Pertanian
(CSIRO) Commonwealth Scientific and Industrial Research Organization. 1983. Soybean response to
controlled waerlogging. P.4-8. In R. Lehane (ed) Rural Reseach. The Science Communication of
CSIROs Beaureau of Scientific Services.
Djayusman, M., I.W. Suastika, Y. Soelaeman. 2011. Refleksi pengalaman dalam pengembangan sisatem usaha
pertanian di lahan pasang surut, Pulau Rimau . Seminar Hasil Penelitian Pengembangan Sistem Usaha
Pertanian Lahan Pasang Surut Sumatera Selatan. Badan Penelitian dan Pengmbangan Pertanian,
Pusat Penelitian dan Penmbangan Tanah dan Agroklimat. Bogor, Juni 2011. Hal 1-20.
Ghulamahdi, M., F. Rumawas, J. Wiroatmodjo, J. Koswara. Pengaruh pemupukan fosfor dan varietas terhadap
pertumbuhan dan produksi kedelai pada budidaya jenuh air. Forum Pasca Sarjana. 14(1):25-34
Ghulamahdi, M., SA Aziz., M Melati, N Dewi dan SA Rais. 2006. Pengaruh genotipe dan pupuk daun terhadap
pertumbuhan dan produksi kedelai panen muda pada budidaya jenuh air. Bul. Agron. 34(1):32-38.
Ghulamahdi, M., 2008. Pengaruh genotip dan pupuk daun terhadap pertumbuhan dan produksi kedelai panen
muda pada budidaya jenuh air. J. Agripeat. 9(2): 49-54
Ghulamahdi, M., E. Nirmala. 2008. Pengaruh waktu pemetikan dan genotip tehadap pertumbuhan dan produksi
kedelai pada budidaya jenuh air. Anterior J. 8(1):6-13.
Ghulamahdi, M., M. Melati, and D. Sagala. 2009. Poduction of soybean varieties under saturated soil cultura on
tidal swamps. J. Agron. Indonesia. 37(3):226-232.
Indradewa, D., S. Notohadisuwarno, S. Sastrowinoto dan H. Prabowo. 2002. Lebar bedengan untuk genangan
dalam parit pada tanaman kedelai. Bul. Agron. 30(3):82-86.
Indradewa, D., S. Sastrowinoto., S. Notohadisuwarno dan H. Prabowo. 2004. Metabolisme nitrogen pada
tanaman kedelai yang mendapat genangan dalam parit. Bul. Agron. 11(2):68-75.
Irwan, A.W. 2006. Budidaya Tanaman Kedelai (Glycine max (I.) Merrill). Jurusan Budidaya Pertanian Faperta.
Unpad. Jatinangor. 40 hal.
Noor, A, and A. Sabur. 2007. Hasil padi varietas unggul pada dua cara penyiapan lahan di lahan pang surut
Kalimantan Selatan. Prosiding Seminar Nasional Sumberdaya Lahan dan Lingkungan Pertanian Badan
Penelitian dan Pengembangan Pertanian Departemen Pertanian 7-8 November 2007. Hal 27-35
Suwarto., W.Q. Mugnisjah, D. Sopandie dan A.K. Makarim. 1994. Pengaruh pupuk nitrogen dan tinggi muka air
tanah terhadap pertumbuhan bintil akar, pertumbuhan dan produksi kedelai. Bul. Agron. 22(2):1-5.
Troedson, R.J., R.J. Lawn, D.E. Byth, G.L. Wilson. 1985. Saturated soil culture in innovated water management
option for soybean in the tropics and subtropics. P 171-180. In S. Shanmugasundaran and E. W.
Sulzberger (Eds). Soybean in Tropical and Sustropical System. AVRDC, Shanhua, Taiwan.

th
Agronomic Performance of F7 Large Seed Soybean Breeding Lines
in Medium Plains

Darman M. Arsyad
a,*
Asadi
b

a
Central Institute for Agricultural Technology Assessment and Development, Bogor, Indonesia
b
Research Institute for Agricultural Biotechnology and Agricultural Genetic Resources, Bogor, Indonesia
* Corresponding author: Central Institute for Agricultural Technology Assessment and Development,
Bogor, Indonesia
Tel: +62-251-8351277; Fax: +62-251-8350928
[email protected]

Abstract

Hybridization between different genotypes aims to obtain descents (breeding lines) which inherits with the good
characters of both parents. One of the soybean breeding program is directed to obtain new varieties with higher
yield potential, wide adaptation, desirable agronomic traits and large seed. A total of 60 F7 soybean breeding
lines (origin crosses of Tanggamus x Local Tegal , Sibayak x Local Tegal, and Sibayak x Argomulyo), selected
in 2007, and four large seed standard varieties (Argomulyo, Burangrang, Anjasmoro, and Panderman) were
evaluated in rice fields, Sukasono Village, Sukawening Subdistrict, Garut District, West Jawa, Indonesia (at 700
m above sea level) on the early dry season (February-May) 2008. A randomized block design with three
replicates was used. Experimental plot size was 0.9 x 4.0 m, spacing of 45 x 10 cm, one plant per hill. Intensive
techniques cultivation involves fertilizing with 75 kg urea, 200 kg SP36, and 150 kg KCl per ha, controlling of
weeds, pests and diseases were carried out. Irrigation was applied when there was no rain. The results showed
that there was variability of seed yield and agronomic traits among the breeding lines tested. Among the 60 F7
breeding lines, eight lines were significantly better yield than Anjasmoro (best standar variety), namely U-719-1-
1, U-509-1-1, U-714-1-1, V-159-1-3, V-426-1-2, V-421-1-1, V-563-1-1, and V-570-1-2 with a yield capacity
ranged from 2.5 to 2.7 t/ha, meanwhile Anjasmoro yielded at 2.3 t/ha. Breeding lines of U-719-1-1 and U-714-1-
1 had a moderate seed size (12.0 to 12.5 g/100 seeds); V-159-1-3 and V-570-1-2 had a slightly large seed (13.6
g/100 seeds), and U-509-1-1, V-426-1-2, V-421-1-1 and V-563-1-1 had a large seed (14.6 to 15.6 g/100 seeds).
Breeding line with the U and V code were derived from Tanggamus x Lokal Tegal and Sibayak x Local Tegal
crosses, respectively. Plant height was suggested as a criterion of selection for high yield.

Keywords: soybean, high yield, large seed

Introduction

The availability of improved varieties of high yielding, early maturity or moderate, and good
seed quality are needed for increasing the domestic soybean production. Today the preferences of
users (farmers and craftsmen tempeh and tofu) were more likely to require large varieties of
soybean seed. Craftsmen tempeh and tofu has long accustomed to using large seed soybean
imports, so that preferences are now a lot towards the large seed. To meet user demand, then
breeding programs to produce varieties of soybean large seed in major need of attention. A number
of varieties of soybean large seed has been available as Argomulyo, Burangrang, Anjasmoro, and
Grobogan (Hermanto et al., 2009).
In an effort to produce new varieties of soybeans are superior to varieties already exist, a
number of crossing (hybridization) between the genotypes having high yield potential, adaptation is
quite broad, many pods and smaller seeds with the genotypes of the large seed, few pods, narrow
adaptation and relatively low yield potential was created in 2004 (Arsyad et al. 2005). Arsyad and
Asadi (2011) reported that amount of 4800 F4 lines originated from five single cross combination
were planted in ricefield, Sukawening, Garut District, West Java on early dry season 2007. By using
pedigree method of selection, 1311 F5 lines were selected and grown in similar site on late dry
th
season 2007. Amount of 540 F6 lines were selected and grown in similar site on early rainy season
2007/2008. Sixty-two F7 lines were selected and 42 lines among them had high yield and large
seed size.
This study aims were to: (a) obtain F8 lines better than comparable variety of Anjasmoro,
having the higher yield potential, good agronomic traits, and has a large seed size or slightly larger,
and (b) investigate the behavior of the relationship between traits in soybean breeding lines.


A total of 60 F7 soybean breeding lines (origin crosses of Tanggamus x Local Tegal,
Sibayak x Local Tegal, and Sibayak x Argomulyo) selected in 2007, and four large seed standard
varieties (Argomulyo, Burangrang, Anjasmoro, and Panderman) were evaluated in rice fields,
Sukasono Village, Sukawening Subdistrict, Garut District (700 m above sea level) on the early dry
season (February-May) 2008. A randomized block design with three replicates was
used. Experimental plot size was 0.9 x 4.0 m, spacing of 45 x 10 cm, one plant per hill. Intensive
techniques cultivation involves fertilizing with 75 kg of urea, 200 kg of SP36, and 150 kg of KCl per
ha, controlling of weeds, pests and diseases were carried out. Irrigation was applied, if there is no
rain. Observations were made on days to maturity, plant height, number of branches, number of
pods, seed yield, 100 seed weight. Analysis of variances was performed on the characters
observed and followed by LSD (Gomez and Gomez 1984), and inter-character correlation and path
analysis followed Singh dan Chaudhary (1979).

Result and Discussion

Analysis of variances showed that there were significant different among the breeding lines
tested against agronomic performances such as yield, seed size (weight of 100 seeds), plant height
and number of pods per plant (Table 1). The range of seed yield of the 60 lines tested ranged from
1.53 to 2.65 t/ha, whereas the yield of four check varieties ranged from 1.47 to 2.30 t/ha. Large
seeds (based on 100 seed weight) of 60 lines tested ranged from 10.3 to 20.7 g, and four check
varieties had 100 seeds weight from 14.7 to 19.4 g. The breeding lines selected were those with
100 seed weight over 14 g. Based on these criteria, 32 lines were selected. The best check variety
(Anjasmoro) with the yield of 2.3 t/ha and 100 seed weight was 14.7 g, while three other check
varieties gave lower yield (1.5 to 2.0 t/ha).
By using Anjasmoro as a comparison, the eight lines significantly better, namely U-719-1-
1, U-509-1-1, U-714-1-1, V-159-1-3, V-426-1-2, V-421-1-1, V-563-1-1, and V-570-1-2. Two lines,
namely U-719-1-1 and U-714-1-1 had a moderate seed size (12.0 to 12.5 g/100 seeds), two other
lines of V-159-1-3 and V-570-1-2 had a slightly large seed size (13.6 g/100 seeds), and four other
lines of the U-509-1-1, V-426-1-2, V 421-1-1 and V-563-1-1 had a large seed size (14.6 to 15.6
g/100 seeds). There were 27 other lines that have a large seed size (> 14 g/100 seeds), but the
yield was lower or equal to Anjasmoro.
The results of the preliminary yield test of F7 lines showed that there were the best five
lines derived from cross of Sibayak x Local Tegal and three lines derived from cross of Tanggamus
x Tegal, while lines derived from cross of Sibayak x Argomulyo nothing was selected. All F7 lines
tested in this study had a yellow seed color, and the seeds was classified as moderate, rather large
and large. Genotypes (parents) who are used to form the lines tested in this study had a medium
seed size (Sibayak), rather small (Tanggamus) and large (Local Tegal and Argomulyo).

th
Table 1. Seed yield, 100 seed weight, number of plant harvested, plant height, number of pods per plant, and
days to maturity of F7 soybean breeding lines in Garut, early dry season 2008

No.

Breeding line
Seed
yield
(t/ha)
100 seed
weight (g)
Number of
plant
harvested
per 3.6 m
2

Plant
height (cm)
Number of
pods per plant
Days to
maturity
1 U-788-1-1 1.91 12.5 42 66 43 84
2 U-121-1-1 1.76 12.9 45 59 53 84
3 U-719-1-1 2.46 12.0 50 67 55 85
4 U-562-2-2 1.53 12.4 39 52 56 84
5 U-534-3-1 2.10 15.1 38 66 49 85
6 U-511-1-1 1.93 12.7 47 74 51 85
7 U-79-2-2 1.84 13.6 42 62 46 88
8 U-79-2-3 2.02 14.2 47 55 46 89
9 U-509-1-1 2.49 15.6 48 65 58 89
10 U-508-3-1 2.00 15.0 48 69 45 90
11 U-601-1-1 1.70 13.6 47 68 41 90
12 U-622-1-1 2.24 13.3 48 73 49 87
13 U-622-1-2 2.21 13.7 46 56 46 89
14 U-464-1-1 2.34 12.5 54 64 59 88
15 U-76-2-1 2.07 12.3 52 58 47 91
16 U-221-1-1 2.22 12.3 45 58 42 92
17 U-142-1-1 2.25 13.2 53 66 49 85
18 U-505-1-1 2.27 14.2 44 67 52 90
19 U-805-1-1 2.37 14.2 46 69 50 90
20 U-714-1-1 2.50 12.5 55 63 56 86
21 U-553-1-1 2.20 12.6 47 63 46 86
22 U-512-1-1 2.11 14.5 43 54 44 92
23 U-675-1-1 2.25 13.3 51 63 46 90
24 U-542-1-1 2.12 14.9 43 58 38 83
25 U-568-1-1 1.69 13.5 40 52 40 89
26 U-788-1-1 2.09 10.8 39 61 63 93
27 V-4-1-2 2.32 14.9 48 66 48 91
28 V-92-1-2 2.16 16.0 40 70 44 92
29 V-129-1-1 1.80 14.3 38 75 40 92
30 V-129-1-2 2.07 16.9 47 77 30 91
31 V-129-1-3 2.05 14.6 46 70 39 87
32 V-158-2-1 2.09 13.7 49 68 45 86
33 V-159-1-3 2.52 13.6 51 78 49 86
34 V-160-1-1 2.04 13.6 39 68 58 86
35 V-180-1-2 2.30 15.1 56 81 46 91
36 V-180-1-3 1.94 15.0 48 69 39 91
37 V-273-2-3 1.75 15.2 39 76 45 89
38 V-284-2-2 2.33 14.5 52 81 37 89
39 V-284-2-3 2.36 14.4 48 77 53 89
40 V-296-1-1 1.94 15.2 45 67 45 93
41 V-296-1-3 1.94 15.2 38 74 53 93
42 V-215-1-1 2.01 13.5 47 73 40 89
43 V-342-1-1 2.25 13.8 48 94 51 89
44 V-426-1-2 2.50 14.6 51 82 52 89
45 V-421-1-1 2.65 15.2 46 86 47 88
46 V-421-1-2 2.39 14.5 53 71 44 93
47 V-424-1-3 1.87 15.1 43 65 47 91
48 V-468-1-2 2.04 14.3 47 66 48 91
49 V-503-1-1 1.59 14.6 38 55 45 93
50 V-563-1-1 2.63 15.3 46 72 40 89
51 V-570-1-2 2.61 13.6 49 71 47 92
52 V-579-1-1 2.13 13.0 44 71 51 91
53 V-933-2-1 1.80 14.6 41 77 44 88
54 V-933-2-2 1.99 20.7 39 69 36 86
55 V-1118-1-1 1.88 16.2 42 66 44 82
56 V-1118-1-3 1.95 16.8 47 72 39 94
57 W-104-2-1 1.79 12.6 44 62 56 92
58 W-38-1-1 2.06 14.6 53 83 46 93
th
59 W-38-1-2 2.04 12.7 51 74 42 95
60 W-106-1-3 2.37 10.3 58 79 58 89
61 Argomulyo 1.47 15.9 51 52 22 80
62 Burangrang 2.00 15.7 49 74 40 81
63 Anjasmoro 2.30 14.7 44 76 35 85
64 Panderman 1.60 19.4 38 59 38 95
Breeding lines
LSD .05
CV (%)
**
0.12
13.1
**
1.3
6.8
**
10
13.9
**
12
10.9
**
14
19.2
-
-
-
Breeding lines of U code was from Tanggamus x Tegal cross; Breeding lines of V code was from Sibayak x Tegal cross;
Breeding lines of W code was from Sibayak x Argomulyo cross

In the plant breeding needs to investigate the relationship (correlation) between
characters. If the selection is done on a character, we need to observe how they affect other
characters (Burton, 1983). Analysis of correlation between traits in this study showed that seed
yield had the strongest positive correlation with the number of plants in both F7 populations (lines)
(Table 2). The greater the number of plants the higher plants and the higher the seed yield. The
pattern of relationships among characters in Tanggamus x Tegal population seemed to differ from
the Sibayak x Tegal population.
The study also found that seed yield did not correlate with weight (large) seed, but Susanto
et al. (2001) reported that seed yield was positively correlated with large seeds. This suggested that
there were opportunities to obtain lines of high yielding and large seeds. The results also found that
the bigger the seed the less number of pods. This indicates that it would be difficult to obtain large
seed lines by the high number of pods. To get maximum yield for the lines of large seed, let the
optimum environmental conditions, so that seed filling goes well.
Dynamic relationship between the characters can be decomposed into two components,
namely direct and indirect effects (Singh and Chaudhary 1979). The pattern of direct effect between
the two populations seem to differ (Tables 3 and 4). In the cross of Tanggamus x Tegal, a strong
direct effect was shown by the number of pods and number of plants, while in the cross of Sibayak
x Tegal indicated by plant height and number of pods. Direct effect of pod number and plant number
in the cross of Tanggamus x Tegal poorly supported by the results of the other components (Table
3). Direct effect of plant height in crosses Sibayak x Tegal also poorly supported by the results of
the other components, but direct effect of pod number somewhat weakened by 100 seed weight
(Table 4).
Characters that can be used as selection criteria for yield is the yield component that has a
positive correlation with the yield and have a large direct effect on yield, and yield components
which have a large positive direct effect (although less correlated with the outcome) (Board et al.
1997). Based on this, it appears that plant height and pod number are considered as selection
criteria in soybean. In the field work selection, the use of pod number and plant height were also
more practical compared with other characters.

Table 2. Correlation between characters of F7 soybean breeding lines in Garut, early dry season 2008

Character Seed yield
100 seed
weight
Number of
plants
Plant
height
Number of
pods
Days to
maturity
Seed yield 0,090 0,574** 0,348 0,327 0,146
100 seed weight -0,197 -0,125 0,066 -0,365 0,012
Number of plants 0,662** -0,272 0,325 0,174 0,016
Plant height 0,484** -0,119 0,387** 0,190 -0,148
Number of pods 0,192 -0,526** -0,050 0,084 -0,021
Days to maturity -0,095 -0,074 0,040 -0,133 -0,062
Value above and below diagonal represented for Tanggamus x Tegal (N=26) and Sibayak x Tegal (N=30), respectively
** significant at P. 0.01

th
Table 3. Direct effect (in diagonal) and indirect effect of yield component on yield of 26 F7 soybean breeding
lines of Tanggamus x Local Tegal in Garut, early dry season 2008

Character Number of
plants
Plant
height
Number of
pods
100 seed
weight
Days to
maturity
Total
effect
Number of plants 0.544 -0.133 0.159 0.008 -0,003 0,575
Plant height 0.177 -0,408 0,173 -0.004 -0,026 -0,088
Number of pods 0.095 -0.078 0,911 0,022 -0,004 0,946
100 seed weight -0.068 -0.027 -0.333 -0,060 -0,002 -0,490
Days to maturity 0,042 -0,299 0,094 -0,004 -0,036 -0,203

Tabel 4. Direct effect (in diagonal) and indirect effect of yield component on yield of 30 F7 soybean breeding
lines of Sibayak x Local Tegal in Garut, early dry season 2008
Character Number of
plants
Plant height Number of
pods
100 seed
weight
Days to
maturity
Total
effect
Number of plants -0,022 0.724 0.012 -0.029 0,002 0,687
Plant height -0,009 1,870 0,020 -0.013 -0,006 1,862
Number of pods 0.001 0.157 0,238 -0,057 -0,003 0,336
100 seed weight 0.060 -0.223 -0.125 0,108 -0,003 -0,183
Days to maturity -0,001 -0,249 -0,015 -0,008 0,045 -0,228

Acknowledgment

The authors would like to acknowledge the support of the Indonesian Ministry of Research and
Technology, for providing the funding for this research.

References

Arsyad DM and Asadi. 2011. Selection of F4, F5 and F6 soybean breeding lines for high yield and large seed
size. Paper presented at The 7
th
Asian Crop Science Association Conference. Bogor, Indonesia. 27-30
September 2011.
Arsyad DM, H Kuswantoro and Purwantoro. 2005. Hybridization, and selection penggaluran
soybeans. Technical Report Research Institute for Crop Legumes and Tuber (In Indonesian).
Board JE, MS Kang and BG Harville. 1997. Path analysis identify selection criteria for yield of late planted
soybean. Crop Sci. 37 (1):879-884.
Burton JW. 1983. Quantitative genetics: Results relevant to soybean breeding, p. 211-248. In J. R. Wilcox (Ed.):
Soybean: Improvement, Production, and Uses. Second Edition, ASA, Wisconsin, No. 16 in series.
Fehr WR. 1983. Applied Plant Breeding. Dept. of Agronomy, Iowa State Univ. Ames. 174 p.
Gomez KA and AA Gomez. 1984. Statistical Procedures for Agricultural Research. 2nd Edition. Pp 680.
Heriyanto. 2006. Deployment and utilization of soybean varieties as raw materials industry and the
competitiveness of commodities in East Java. Crop Bulletin Research Institute for Crop Legumes and
Tuber (In Indonesian) No.11:52-68.
Hermanto, D Sadikin and E Hikmat. 2009. Deskripsi Varietas Unggul Palawija 1918-2009. Indonesian Center for
Food Crops Research and Development. Indonesian Agency for Agriculture Research and Development.
Pp 330 (In Indonesian).
Singh ID and BD Chaudhary. 1979. Biometrical Methods in Quantitative Genetic Analysis. Kalyani Publ. New
Delhi. Pp 301.
Susanto, M. Jamaluddin, T Sanbuichi, N Sekiya, DM Arsyad and MM Adie. 2001. Large high quality seed and
promising lines selected from Mansuria as candidates of new varieties, p. 7-16. In Roesmiyanto et
al. (Eds.): Forum on Soybean Seed Production in East Java. JICA-Indonesian Ministry of Agr.


th
Organically Production of Soybean Supported by Fertilizers Residue under
Saturated Soil Culture

Maya Melati
a,*
, Kalimatul Jumro
a

a
Department of Agronomy and Horticulture, Faculty of Agriculture, Bogor Agricultural University, Indonesia
* Corresponding author: Department of Agronomy and Horticulture, Faculty of Agriculture,
Bogor Agricultural University (IPB).
Jl. Meranti, Kampus IPB Darmaga, Bogor 16680, Indonesia.
Tel.: +62 251 8629353; fax: +62 251 8629353.
[email protected]

Abstract

Organic farming system can use natural on-farm inputs that are normally available at the production site.
Saturated Soil Culture (SSC) is a technology in cultivation that gives water permanently, maintains and keeps its
depth constantly; this makes soil layer in saturated condition. SSC technology can be implemented in land with
poor drainage or in cultivating soybean on rice field in the period between two rice plantings when the soils may
still be in water saturated conditions. The experiment was conducted to study the response of two soybean
varieties to the residues of different types of fertilizer in an organic farming system. The experiment was carried
out at IPB experimental station, Bogor, Indonesia, in October 2010-February 2011. Split plot design was used
with types of fertilizer as the main plot (chicken manure, Centrosema pubescens Benth, and Tithonia diversifolia
Hemsl.) and soybean varieties as the sub plot (Anjasmoro and Wilis). To study the effectiveness of fertilizers
residue, the current experiment applied 50% fertilizer rates (10 t chicken manure only/ha, 5 t chicken manure
mixed with 2.1 t C. pubescens/ha, and 5 t chicken manure with 2.1 t T. diversifolia/ha) of those applied in the
previous soybean planting (May-August 2010). The results showed that chicken manure yielded the highest
seed weight and filled pod number per plant. However, seed yields per hectare were not affected by fertilizer
types. The soybean plant with the application of chicken manure, C. pubescens, and T. diversifolia produced
2.37, 2.42, and 2.43 t seed/ha, respectively. Wilis had higher number of filled pod per plant than Anjasmoro, but
the yields per hectare of both varieties were not different. Production of Anjasmoro and Wilis was 2.43 and 2.38
t/ha, respectively.

Keywords: Centrosema pubescens Benth, chicken manure, Glycine max (L.) Merr., green manure, Tithonia
diversifolia Hemsl

Introduction

National demand on soybean is about 2.2 million tons per year, but only 35-40% of this
demand can be supplied from the domestic production, and the government has to import about 1.3
t soybean/year. Low productivity, decreasing agricultural land area, and limited access of farmers to
technology and funding, are some of the factors restricting the national production of soybeans.
Organic farming is an alternative to currently used methods of farming; its use might
increase soybean production. Currently the marketing of produce from organic farms is targeted
only at consumers who are interested in it because they view it as being healthier. However,
organic farming systems could be useful to farmers who have limited access to production inputs
(e.g. inorganic fertilizers and pesticides) and funds. Because of the presumed lower productivity of
organic systems as opposed to conventional farming the ability of organic systems to support food
security is questioned; nevertheless organic farming may be able to provide local food security.
Farmers can use on-farm inputs normally available to them on the site of production.
Organic farming system had been used to produce vegetable soybean with various types
of fertilizer, for example chicken manure, green manure of Calopogonium mucunoides, Centrosema
th
pubescens, and Crotalaria juncea, rock phosphate, charcoal and ash or rice hull (Barus, 2005;
Melati and Andriyani, 2005; Sinaga, 2005; Kurniasih, 2006). Some of those organic fertilizers had
resulted significant differences in plant performances, but not in production. The experiment had
also been conducted to produce dry seed of soybean to investigate whether organic farming system
supported plant production not only at less mature seed but also at fully mature stage. Kurniansyah
(2010) found that chicken manure only or its combination with green manure produced dry seed of
1.16-1.48 t/ha on upland, while Ramadhani (2011) found that soybean yield was 1.83-1.94 t/ha on
soil with saturated soil culture technology.
Saturated Soil Culture (SSC) is a technology in cultivation that gives water permanently,
maintains and keeps its depth constantly (about 5 cm under soil surface); this makes soil layer in
saturated condition. In saturated soil culture, watering is started from the beginning of plant growth
to maturity stage (Hunter et al., 1980). By keeping the water-table constantly, soybean will be
avoided from negative effect of inundation on soybean growth, because soybean will acclimatize
and improve its growth (Troedson et al., 1983). Ghulamahdi (2007) found that under SSC, growth
and production of soybean was improved related to the increase of ACC, ethylene, glucose content,
and neck diameter of roots, and the increase of nodules weight, nitrogenase activity, and nutrient
uptakes. SSC technology can be implemented in land with poor drainage or in cultivating soybean
on rice field in the period between two rice plantings where the soils may still be in water saturated
conditions. Ghulamahdi et al. (2009) also showed that SSC can be implemented in cultivating
soybean in tidal swamp area with the production of more than double of those in upland.
The availability of nutrient provided by organic fertilizers is not as quick as from inorganic
fertilizers; this may result in available nutrient in the following cropping season. Melati et al. (2008)
showed that the residue of fertilizers supported the production of organic vegetable soybean on
upland soil. The current experiment studied the possibilities of producing dry seed of soybean with
the residue of fertilizers under SSC technology. Two types of soybean cultivar (they differ in seed
sizes) were used to investigate their responses to the treatments.


A field study was conducted in October 2010-February 2011 at the Cikarawang
Experiment Station of Bogor Agricultural University (IPB), in Bogor, Indonesia. The soil is a silty clay
loam soil. The experiment was the second crop sequence. The experimental design was a
randomized complete block with spilt plot arrangement and three replicates. Types of fertilizer
included in the study were chicken manure only (10 t/ha), chicken manure combined with
Centrosema pubescens (5 + 2.1 t/ha), and chicken manure combined with Tithonia diversifolia (5 +
2.1 t/ha) were considered as main plots, and assigned to an area of 4 x 4 m. Subplots were
assigned within each main plot, each differing by soybean cultivar, i.e. Anjasmoro and Wilis.
Subplots dimensions were five 4-m long rows spaced 0.4 m apart and 0.1 m apart within row.
Those fertilizer rates were half of rates in the first crop sequence to evaluate the
effectiveness of fertilizers residue. In the first crop sequence, the rate of chicken manure was
applied at the rate of 20 t/ha followed Sinaga (2005) and the rates of green manure biomass was
determined based on a study of Kurniasih (2006). It was expected that a yield of about 10 t
biomass/ha

was obtained

from 25 kg seed of C. pubescens. However, dry conditions during the
growth period of C. pubescens. (December 2009-April 2010) resulted in the production of only 3.5 t
C. pubescens biomass/ha. Although Tithonia diversifolia could be easily collected from a nearby
area, it was also applied at the rate of 3.5 t/ha to make appropriate comparisons with the use of C.
pubescens. Besides those fertilizers according to the treatments, all plots were added with 1 t rice
hull charcoal and 1 t dolomite per hectare. Green manure (combined with chicken manure, rice hull
charcoal and dolomite) was applied 4 weeks before soybean planting, while chicken manure (plus
th
rice hull charcoal and dolomite) was applied 2 weeks before soybean planting. All materials were
applied in planting rows; they were then below the position of soybean seed.
SSC technique was conducted by providing water permanently since 4 weeks after
planting (WAP), maintained and kept water depth constantly at about 5 cm under soil surface in 20-
cm depth furrow. Ghulamahdi (2007) found that plants normally experience chlorosis in saturated
soil, therefore, in the current experiment liquid manure (1 L liquid manure/10 L water) was added as
foliar application to the plants at the 3
rd
, 5
th
, and 7
th
day after irrigation began.
Other cultural practices were seed treatment by using Rhizobium inoculants with the rate
of 6.25 g/kg seed, and the planting of Tagetes erecta and Cymbopogon nardus near soybean plants
to control plant pest and diseases. Tagetes erecta and Cymbopogon nardus had been used in
producing organic vegetable soybean (Kusheryani and Aziz, 2006).
Analysis of variance was used to analyze the data and Duncan Multiple Range Test
(DMRT) was used to compare means value.


Plant characters as shown in vegetative phase and yield component in generative phase
were not different among fertilizer types. Variables were only different in number of filled pod and
seed yield per plant with the highest values were in plants with the application of chicken manure
only. Since the number of harvested plant in plot with chicken manure only was lower than those
with other fertilizers, seed yields per hectare were not different among treatments (Table 1).

Table 1. Plant characters and production with three types of fertilizer

Variables
F
test
Fertilizers
Means
Tithonia
diversifolia
Chicken
manure only
Centrocema
pubescens
Vegetative phase
Plant height at 7 WAP (cm) ns 88.05 85.85 84.99
86.30
Plant height at harvest/ 14 WAP (cm) ns 94.09 91.28 90.46 91.94
Trifoliate leaf numbers/plant ns 18.5 19.5 18.3
18.8
Pest intensity (%) ns 28.9 30.8 29.4
29.7
Disease intensity (%) ns 8.8 10.6 8.5
9.3
Dry weight of leaves (g/plant) ns 5.92 6.04 7.21 6.39
Moisture content of leaves (%) ns 64.9 64.5 67.2 65.5
Nitrogen content in leaves (%) ns 3.3 3.2 3.2
3.2
Phosphorus content in leaves (%) ns 0.5 0.5 0.5 0.5
Potassium content in leaves (%) ns 2.9 2.8 2.9
2.9
N uptake of leaves (mg/plant) ns 19.47 19.66 23.04
20.72
P uptake of leaves (mg/plant) ns 3.17 3.01 3.70 3.29
K uptake of leaves (mg/plant) ns 17.26 16.99 21.52
18.59
Generative phase
Dry weight of shoot (g/plant) ns 20.77 26.60 26.25
24.54
Numbers of filled pod/plant * 93.0b 111.7a 99.3b
101.3
Numbers of harvested plant/4.56 m
2
ns 118.8 104.0 112.0 111.6
Seed weight (g/100 seeds) ns 15.17 15.83 16.00
15.67
Seed yield (g/plant) ** 25.33b 32.65a 28.25ab
28.74
Seed yield (g/4.56 m
2
) ns 1109.67 1082.50 1101.17 1097.78
Seed yield (ton/ha) ns 2.43 2.37 2.42 2.41
Note: ns = not significant; * and ** = significant at p < 0.05 and p < 0.01, respectively. Numbers followed by letters indicating
different at = 5% with DMRT.
th
Seed yield per plant may be related to the soil nutrient content. After the 1
st
crop season,
C-organic, N-total, available P and K were higher in plots with the application of chicken manure
only compared to those with other fertilizer treatments. These conditions were also detected in the
2
nd
crop sequence before soybeans were planted (Table 2). The amount of nutrients in the soil with
chicken manure application had supported the seed yield of single plant.

Table 2. Soil characteristics

Treatments
pH
H
2
O
Walkly &
Black
Kjeldhal Bray l N NH
4
Oac pH 7.0
Fertilizers Varieties
C-org N-Total P K Mg Ca Na KTK
..(%).. ..(%).. (ppm) ..(me/100g)..
After 1
st
crop sequence
Chicken m. Anjasmoro
6.37 2.20 0.20 25.43 0.89 2.83 6.37 0.74 16.56
Chicken m. Wilis
6.63 2.04 0.20 17.23 0.85 2.82 7.98 0.54 15.87
Tithonia sp. Anjasmoro
6.53 1.84 0.18 9.20 0.86 2.60 7.42 0.59 15.80
Tithonia sp. Wilis
6.67 1.89 0.19 15.57 0.60 2.41 6.66 0.51 14.77
Centrosema Anjasmoro
6.40 1.76 0.17 6.15 0.69 2.74 6.98 0.45 16.68
Centrosema Wilis
6.40 1.68 0.17 5.55 0.52 2.24 6.39 0.41 15.86
After application of fertilizers in the 2
nd
crop sequence
Chicken m. Anjasmoro 6.30 2.63 0.22 33.50 n.a. 3.06 7.94 0.61 17.76
Chicken m. Wilis 6.50 2.55 0.22 28.80 2.90 7.82 0.48 18.36
Tithonia sp. Anjasmoro 6.40 1.60 0.15 8.50 3.57 8.72 0.47 21.45
Tithonia sp. Wilis 6.60 1.68 0.15 12.70 3.26 8.32 0.64 18.37
Centrosema Anjasmoro 6.60 2.00 0.19 25.00 3.78 8.46 0.80 18.16
Centrosema Wilis 6.30 1.92 0.18 28.70 4.76 9.23 0.75 21.76
After 2
nd
crop sequence
Chicken m. Anjasmoro 7.40 2.79 0.26 31.20 1.42 3.40 8.38 1.16 19.13
Chicken m. Wilis 7.50 2.39 0.22 20.60 1.19 3.00 8.19 1.09 17.95
Tithonia sp. Anjasmoro 7.60 2.23 0.21 14.40 1.11 2.90 7.76 1.06 17.76
Tithonia sp. Wilis 7.50 2.15 0.22 9.00 0.86 2.65 7.42 0.70 16.78
Centrosema Anjasmoro 7.20 2.55 0.23 5.20 0.93 2.55 7.34 1.08 18.35
Centrosema Wilis 7.40 2.55 0.25 16.10 1.18 2.95 8.66 1.07 18.73
Note: Soil samples were composite of 3 replicates from the same treatment, therefore they were not statistically analyzed. n.a.
= valid data were not available

There are some differences in plant characteristics and yield components of the two varieties
in this experiment. These were accordingly with the characteristics of each variety. Anjasmoro has
less number but larger leaves than those of Wilis, therefore, the nutrient uptake was higher in
Anjasmoro. Anjasmoro has less number of filled pod but it has larger seed size, this resulted in
similar seed yield of both varieties (Table 3).

th
Table 3. Plant characteristics and production of two soybean varieties

Variables F test
Varieties
Means
Wilis Anjasmoro
Vegetative phase
Plant height at 7 WAP (cm) * 83.32b 89.29a 86.31
Plant height at harvest/ 14 WAP (cm) ns 91.98 91.91 91.90
Trifoliate leaf numbers/plant * 20.3a 17.2b 18.80
Pest intensity (%) ns 28.9 30.6 29.70
Disease intensity (%) ns 8.8 9.9 9.30
Dry weight of leaves (g/plant) ns 5.39 7.39 6.39
Moisture content of leaves (%) ns 65.5 65.6 65.50
Nitrogen content in leaves (%) ns 3.2 3.3 3.20
Phosphorus content in leaves (%) ns 0.5 0.5 0.50
Potassium content in leaves (%) ** 2.7b 3.1a 2.90
N uptake of leaves (mg/plant) * 17.47b 23.97a 20.72
P uptake of leaves (mg/plant) * 2.77b 3.82a 3.30
K uptake of leaves (mg/plant) * 14.41b 22.76a 18.59
Dry weight of shoot (g/plant) ns 24.77 24.31 24.54
Numbers of filled pod/plant ** 115.4a 87.2b 101.30
Numbers of harvested plant/4.56 m
2
** 122.8a 100.4b 111.60
Seed weight (g/100 seeds) ** 12.11b 19.22a 15.67
Seed yield (g/plant) ns 28.00 29.49 28.75
Seed yield (g/4.56 m
2
) ns 1087.11 1108.44 1097.78
Seed yield (ton/ha) ns 2.38 2.43 2.41
Note: ns = not significant; * and ** = significant at p < 0.05 and p < 0.01, respectively.

Conclusions

The experiment concluded that in the second crop sequence, with half rates of fertilizer, all
types of fertilizer and both varieties could be used to produce similar seed yield per hectare of
organic soybean. In the second crop sequence, there was indication that soil characteristics had
been improved under organic farming system.

References

Barus, LE. 2005. Pengaruh pemberian pupuk hijau dan fosfat alam terhadap pertumbuhan dan produksi kedelai
(Glycine max (L.) Merr) panen muda dengan sistem pertanian organik. Skripsi. Jurusan Budidaya
Pertanian, Fakultas Pertanian. Institut Pertanian Bogor. Bogor.
Kurniasih, W. 2006. Pengaruh jenis, dosis benih dan umur tanaman pupuk hijau terhadap produksi kedelai
(Glycine max (L.) Merr) panen muda organik. Skripsi. Agronomi dan Hortikultura, Fakultas Pertanian.
Institut Pertanian Bogor. Bogor.
Melati, M and W Andriyani. 2005. Pengaruh pupuk kandang ayam dan pupuk hijau Colopogonium mucunoides
terhadap pertumbuhan dan produksi kedelai panen muda yang dibudidayakan secara organik. Bul.
Agron. 33: 8-15.
Sinaga, YAS. 2005. Pengaruh pemberian pupuk organik terhadap pertumbuhan dan produksi kedelai (Glycine
max (L.) Merr.) panen muda yang diusahakan secara organik. Skripsi. Budidaya Pertanian. Institut
Pertanian Bogor. Bogor.
Kurniansyah, D. 2010. Produksi kedelai organik panen kering dari dua varietas kedelai dengan berbagai jenis
pupuk organik. Skripsi. Department of Agronomy and Horticulture. Bogor Agricultural University (IPB).
Bogor.
Ramadhani, E. 2011. The study of fertilizer types for organically production of two soybean varieties under
saturation soil culture technique at two crop sequences (in Indonesia: Kajian aplikasi jenis pupuk untuk
th
produksi dua varietas kedelai secara organik dengan sistem budidaya jenuh air pada dua musim tanam).
Master Thesis. Postgraduate School. Bogor Agricultural University (IPB). Bogor.
Troedson, RJ, RJ Lawn, DE Byth and GL Wilson. 1983. Saturated soil culture in innovated water management
option for soybean in the tropics and sub tropics. In Soybean in Tropical and Subtropical System. Proc.
Symp. Tsukaba. Japan.
Ghulamahdi, M. 2007. Mekanisme Fisiologi Tanaman Kedelai pada Kondisi Jenuh Air dan Kering serta
Kaitannya dengan Biosintesis Etilen. In Seminar Nasional Hasil Penelitian yang Dibiayai oleh Hibah
Kompetitif, 1-2 Agustus 2007. Institut Pertanian Bogor.
Ghulamahdi, M, M Melati and D Sagala. 2009. Production of Soybean Varieties under Saturated Soil Culture on
Tidal Swamps. Agronomy Journal of Indonesia 37: 226-232.
Melati, M, A. Asiah, D. Rianawati. 2008. Aplikasi pupuk organik dan residunya untuk produksi kedelai panen
muda Bul. Agron. 36: 204-213.
Kusheryani, I and SA Aziz. 2006. Pengaruh jenis tanaman penolak organisme pengganggu tanaman terhadap
pertumbuhan dan produksi tanaman kedelai (Glycine max (L.) Merr.) yang diusahakan secara organik.
Bul. Agron. 34: 39-45.

th
Factors Causing the Soybean Yield Gaps between Japan and USA

Keisuke Katsura
a,*
, Koki Homma
a
, Yohei Kawasaki
a
, Larry C. Purcell
b
, Randall L.
Nelson
c
, Taiki Yoshihira
d
a

a
Graduate School of Agriculture, Kyoto University, Japan
b
Department of Crop, Soil and Environmental Sciences, University of Arkansas, AR, USA
c
USDA-Agricultural Research Service, University of Illinois, IL, USA
d
Faculty of Dairy Science, Rakuno Gakuen University, Japan
* Corresponding author: Experimental Farm, Kyoto University, 12-1, Hatchonawate, Takatsuki,
Osaka, 569-0096, Japan.
Tel.: +81 72 685 0134; fax: +81 72 683 1532.
[email protected]

Abstract

The average soybean yield in Japan is stagnated around 1.7 t ha
-1
, which is quite low level compared to that in
USA (around 2.7 t ha
-1
). The objective of this study was to reveal the factors causing this yield gap between
Japan and USA. To examine the variety effect on the yield gap, we conducted yield test at Osaka (central
Japan, 34
o
51N), Hokkaido (northern Japan, 43
o
03N), Feyetteville, AR (south-central USA, 36
o
03N), and
Champaign, IL (mid-western USA, 40
o
06N), in 2009 using 46 Japanese and 510 USA varieties. Averaged
yield of USA varieties was 859 % higher than that of Japanese varieties in each experimental site, which
means the yield potential of USA varieties was higher than that of Japanese varieties. To examine the
environmental effect on the yield gap, we estimated the potential yield (Y
p
) at Hokkaido, Shiga (central Japan,
35
o
16N), Arkansas, AR (south-central USA, 34
o
30N), and Champaign, IL, by simple simulation model, where
we assumed that Y
p
was determined by solar radiation, air temperature and growth duration. Estimated Y
p
in
USA (7.34 t ha
-1
in Arkansas and 7.12 t ha
-1
in Champaign, averaged over recent 30year) was higher than that
in Japan (5.84 t ha
-1
in Shiga and 4.69 t ha
-1
in Hokkaido), and this difference was mainly brought from the
difference in solar radiation intensity. Ratio of the actual yield to the potential yield (Y
a
/Y
p
) was highest in
Champaign (50.7 %, averaged over recent 5year), followed by Hokkaido (44.6 %), Arkansas (38.9 %), and the
lowest in Shiga (24.6 %). In addition, there were increasing tendencies in Y
a
/Y
p
in USA (0.230.50 % year
-1
),
while no such a tendency in Japan. The increasing tendencies in Y
a
/Y
p
in USA would be brought from the
improvement of crop management in addition to breeding new varieties.

Keywords: soybean (Glycine max (L.) Merrill), Yield

Introduction

Improvement on soybean (Glycine max (L.) Merrill) production in Japan is strongly needed,
because soybean self-sufficiency ratio in Japan is quite low (around 5%; MAFF, 2011a). Soybean
yield in Japan has been stagnated around 1.7 t ha
-1
(MAFF, 2011b) in recent years, while that in
USA, the largest producer of soybean in the world, has increased steadily in the last few decades
and reached around 2.7 t ha
-1
(USDA-NASS, 2009). It is not clear, however, how varieties,
environment and crop management have affected on this growing gap soybean yield between
Japan and USA. The objective of this study is to clarify the factors causing soybean yield gaps
between Japan and USA.
In the present study, we grew Japanese and USA commercial soybean varieties in
northern and central Japan and mid-western and south-central USA, where are the major producers
of soybean in Japan and USA. The objectives of this study were (1) to examine the yield potential
(Y
p
) of Japanese and USA varieties and study the varietal effect on the growing yield gap, (2) to
estimate the changes of Y
p
in northern and central part of Japan and mid-western and south-central
USA using a simple simulation model, with the assumtion that Y
p
was determined by solar radiation,
th
air temperature and growth duration, (3) to compare the Y
p
in Japan and USA, and (4) to study the
environmental and crop management effects on the growing yield gap between Japan and USA
bycomparing the changes of Y
a
/Y
p
.


Eight Japanese and 14 USA commercial varieties (Suzukari, Enrei, Suzuyutaka,
Tachinagaha, Sachiyutaka, Tamahomare, Toyomusume and Yuzuru for Japanese varieties and
Athow, Omaha, Manokin, LD003309, 5002T, UA4805, Osage, 5601T, Ozark, Hutcheson, Jack,
Williams82, X34 and X88 for USA varieties) were used in the present study. 46 Japanese and 5
10 USA varieties were grown in Osaka (central Japan, 34
o
51N), Hokkaido (northern Japan,
43
o
03N), Feyetteville, AR (south-central USA, 36
o
03N), and Champaign, IL (mid-western USA,
40
o
06N) during the summer season in 2009. Crop managements, such as sowing date, planting
density, fertilizer application rate, and so on, were based on the common practices in each
experimental site. Experiments were consisted of 3-4 replications. Soybean yield was determined at
maturity by harvesting more than 1m
2
area from each replication.
Based on the meteorological statistics and crop progress reports, changes of Y
p
were
estimated by the following simple simulation model.
( ) { } | |
=
=
d
n
p
Rad LAI k RUE HI Y
1
exp 1
where, HI is harvest index, RUE is radiation use efficiency, k is light extinction coefficient, LAI is leaf
area index, and Rad is solar radiation. LAI was estimated by the logistic function of cumulative
effective temperature with the base temperature being 8
o
C. RUE in Japan was setup at 1.1 g MJ
-1

for preR1+25day period, and 0.77 g MJ
-1
for postR1+25day period, based on the observed
data under ideal conditions in Japan. RUE in USA was setup 10% lower than that in Japan, in
consideration that RUE decreased under intense radiation environment. HI and k were assumed to
be 0.5 and 0.6, respectively.
Potential yield (Y
p
) was estimated for Shiga (central Japan, 35
o
16N), Hokkaido, Arkansas,
AR (south-central USA, 34
o
30), and Champaign, IL. Data from 1980 to 2009 for weather, crop
calendar and statistics of soybean yield in each site were collected. Actual yield (Y
a
) and Y
a
/Y
p
were
analyzed for the field with and without irrigation system separately in Arkansas, because irrigation
system has been rapidly spreading in south-central USA,


The seed yields observed in the variety tests are listed in Table 1. There was large
variation in yield, which ranged from 2.12 to 5.91 t ha
-1
depending on the varieties and sites (Table
1). Averaged yield of USA varieties (4.065.20 t ha
-1
) was 859 % higher than that of Japanese
varieties (2.633.80 t ha
-1
) in each site, which means the yield potential of USA varieties was higher
than that of Japanese varieties.
As for the meteorological statistics in the four assessed locations, there was not so big
difference in effective growth period (98105 days, from emergence to leaf yellowing) among the
sites, while radiation intensity in USA (20.921.4 MJ m
-2
d
-1
) was more than 30 % larger than that in
Japan (15.516.1 MJ m
-2
d
-1
) (Table 2). As a result, estimated Y
p
in USA (78 t ha
-1
) changed
higher than that in Japan (56 t ha
-1
), which showed the soybean potential yield in USA was higher
than that in Japan, mainly because of solar radiation intensity (Figure 1). The values of Y
p
on recent
30-year average in Shiga, Hokkaido, Arkansas, and Champaign were 5.84, 4.69, 7.34, and 7.12 t
ha
-1
, respectively.
th
Actual yield in Japan (1.56 and 2.17 t ha
-1
on recent 30-year average, in Shiga and
Hokkaido, respectively) was lower than that in USA (2.56, 1.72 and 3.04 t ha
-1
on recent 30-year
average, in Arkansas with irrigation system, Arkansas without irrigation system, and Champaign,
respectively) (Figure 1). There were increasing tendencies in actual yield in all the sites, but the
increasing rates were larger in USA (37.3, 20.2 and 35.1 kg ha
-1
year
-1
, in Arkansas with irrigation
system, Arkansas without irrigation system, and Champaign, respectively) than those in Japan (0.9
and 12.5 kg ha
-1
year
-1
, in Shiga and Hokkaido, respectively). In addition, the increasing rates in Y
p

was very small (14.5 and 35.1 kg ha
-1
year
-1
, in USA, which means that the changes in Y
p
could not
explain the recent soybean yield increase in USA.

Table 1. Yield (t ha
-1
) of Japanese and USA soybean varieties grown under Osaka, Feyetteville, Champaign,
and
Hokkaido
in 2009

Table 2. Season of soybean cropping and its climate summary

Latitude
Mean peak date*

Effective
growth
period**
(days)
Total
rainfall
(mm)
Daily temperature Daily solar
radiation
(MJ m
-2
d
-1
) Planting Harvesting
Max
(
o
C)
Min
(
o
C)
Shiga, Jpn 35
o
16 23 Jun 4 Nov 103 581 28.4 21.4 15.5
Hokkaido,
Jpn
43
o
03 23 May 9 Oct 102 333 23.9 16.7 16.1
Arkansas,
USA
34
o
30 24 May 13 Oct 105 261 32.4 21.0 20.9
Champaign,
USA
40
o
06 22 May 4 Oct 98 341 28.7 17.1 21.4
*, based on the crop progress report of Shiga and Hokkaido (1980-1997), East Illinois (1980-2005), and East Central Arkansas
(1996-2008).
**, Emergence to leaf yellowing. The climate data were calculated for the effective growth period based on the meteorological
statistics from 1980 to 2009 for the districts on Japan and USA respectively.

Osaka Hokkaido Feyetteville Champaign
34
o
51'N 43
o
03'N 36
o
03'N 40
o
06'N
Japanese varieties
Suzukari 3.64 4.51 2.85
Enrei 3.93 3.23 2.86
Suzuyutaka 4.13 3.09 2.68
Tachinagaha 3.10 3.44
Sachiyutaka 4.16 3.60
Tamahomare 3.44 3.48
Toyomusume 3.28
Yuzuru 4.32 2.12
Average 3.73 3.80 3.44 2.63
USA varieties
Athow 5.07 4.87 3.88
Omaha 5.91 4.35 4.25
Manokin 5.23 4.70
LD003309 5.06 3.13 4.66
5002T 4.69 5.73
UA4805 5.15 4.44
Osage 5.19 4.72
5601T 5.50 5.32
Ozark 5.19 4.23
Hutcheson 5.03 4.85
Jack 4.04 4.11
Williams82 4.20 3.95
X34 (LJ) 3.61
X88 (LJ) 4.24
Average 5.20 4.06 4.86 4.17
th
y = 0.0243x - 42.592
y = 0.0009x - 0.2955
0
1
2
3
4
5
6
7
8
9
1980 1985 1990 1995 2000 2005 2010
Y
i
e
l
d

(
t

h
a
-
1
)
(a) Shiga, Japan (35
o
16'N)
Yp Ya

y = 0.0272x - 49.445
y = 0.0125x - 22.739
0
1
2
3
4
5
6
7
8
9
1980 1985 1990 1995 2000 2005 2010
Y
i
e
l
d

(
t

h
a
-
1
)
(b) Hokkaido, Japan (43
o
03'N)
Yp Ya

y = 0.0145x - 21.546
y = 0.0373x - 71.845
y = 0.0202x - 38.513
0
1
2
3
4
5
6
7
8
9
1980 1985 1990 1995 2000 2005 2010
Y
i
e
l
d

(
t

h
a
-
1
)
(c) Arkansas, AR, USA (34
o
30'N)
Yp
Ya_irrigated
Ya_non irrigated
y = -0.0045x + 16.19
y = 0.0351x - 66.923
0
1
2
3
4
5
6
7
8
9
1980 1985 1990 1995 2000 2005 2010
Y
i
e
l
d

(
t

h
a
-
1
)
(d) Champaign, IL, USA (40
o
06'N)
Yp Ya

Figure 1. Changes of estimated potential yield (Y
p
) and actual yield (Y
a
) in (a) Shiga, (b) Hokkaido, (c) Arkansas,
and (d) Champaign.

The Y
a
/Y
p
was the largest in Champaign (50.7 %, the recent 5 year average), followed by
Hokkaido (44.6 %), Arkansas with irrigation system (38.9 %), Arkansas without irrigation system
(26.5 %), and the lowest in Shiga (24.6 %) (Figure 2). As is the case in actual yield, there were
increasing tendencies in Y
a
/Y
p
in USA (0.230.50 % year
-1
), while no such tendency in Japan. We
assumed that the increase in Y
a
/Y
p
in USA is brought from the improvement in crop management,
such as increased adoption of irrigation system, introduction of early cultivation and raised bed
planting, improvement in weed management, in addition to the developing and utilizing new high
yielding varieties.
In the present study, we tried to reveal the factors causing the soybean yield gaps between
Japan and USA focusing on environmental, varietal, and technological factors. Our results show
that the greater amount of solar radiation is the major factor of higher yield in the USA and that the
technological developments have caused the increase in yield gap between Japan and USA. There
is still much room for improving soybean yield in Japan.

th
y = -0.0973x + 220.78
0
10
20
30
40
50
60
70
1980 1985 1990 1995 2000 2005 2010
Y
a
/
Y
p
(
%
)
(a) Shiga, Japan (35
o
16'N)

y = 0.0656x - 84.487
0
10
20
30
40
50
60
70
1980 1985 1990 1995 2000 2005 2010
Y
a
/
Y
p
(
%
)
(b) Hokkaido, Japan (43
o
03'N)

y = 0.4352x - 833.06
y = 0.2266x - 428.41
0
10
20
30
40
50
60
70
1980 1985 1990 1995 2000 2005 2010
Y
a
/
Y
p
(
%
)
(c) Arkansas, AR, USA (34
o
30'N)
irrigated
non irrigated
y = 0.4997x - 953.63
0
10
20
30
40
50
60
70
1980 1985 1990 1995 2000 2005 2010
Y
a
/
Y
p
(
%
)
(d) Champaign, IL, USA (40
o
06'N)

Figure 2. Changes of ratio of the actual yield to the estimated potential yield (Y
a
/Y
p
) in (a) Shiga, (b) Hokkaido,
(c) Arkansas, and (d) Champaign.

References

MAFF, 2011a. Table on demand and supply of food, 2009. Association of Agriculture and Forestry Statistics,
Tokyo, Japan.
MAFF, 2011b. Statistics on crops, 2009. Association of Agriculture and Forestry Statistics, Tokyo, Japan.
USDA-NASS, 2009. Crop production reports (http://www.nass.usda.gov/).

th
Photosynthetic Acclimation to Elevated CO
2
in Soybean

Mochamad Arief Soleh
a,b
*, Hai Yan
a
, Tomohiro Konno
a
, Makie Kokubun
a

Ryoji Sameshima
c

a
Graduate School of Agricultural Science, Tohoku University, Japan
b
Faculty of Agriculture, Padjadjaran University, Indonesia
c
National Agricultural Research Center for Tohoku Region, Japan
[email protected]

Abstract

Previous studies on plant responses to elevated atmospheric CO
2
concentration [CO
2
] found the occurrence of
elevated [CO
2
]induced photosynthetic acclimation. Soybean cultivar Enrei was grown in pots and was
subjected to either ambient [CO
2
] (ca. 380 mol mol
-1
) or elevated [CO
2
] (ca. 580 mol mol
-1
) regime. The half of
the plants were transferred to the other [CO
2
] regime at flowering. Under elevated [CO
2
], photosynthetic rate was
markedly enhanced at the early growth stage, whereas it was decreased at the later growth stage on both
transferred and untransferred plants, indicating that the acclimation occurred at the later growth stage of the
plants regardless of the transfer. Electron transport rate (ETR) curve of the plants under elevated [CO
2
] regime
became plateau at about 300 mol mol
-1
intercellular [CO
2
] at the later growth stage (35 days after transfer
(DAT)), which was less than the plateaued value under ambient [CO
2
] regime (320 mol mol
-1
), indicating that
the acclimation of photosynthesis occurred due to decreased intercellular [CO
2
] which might be restricted by the
decrease in stomatal conductance, N or chlorophyll content in leaves. Moreover, the leaf N and chlorophyll
content (SPAD reading) of the plants grown under elevated [CO
2
] regime was lower than those of the plants
grown under ambient [CO
2
] regime at the later growth stage (80 days after sowing (DAS)/32 DAT). Thus the
acclimation of photosynthesis of soybean appeared to be induced by decreases in stomatal conductance, N or
chlorophyll content in leaves, although other factors such as starch accumulation in leaves at the later growth
stage, which can restrict Rubisco activity in leaves, might be involved in the acclimation. Further research is
needed to examine how other possible factors are involved in the acclimation of photosynthesis.

Keywords: elevated [CO
2
]; photosynthesis.

Introduction

Increasing [CO
2
] in the atmosphere will offset increased photorespiration by increasing
photosynthesis, especially in plants with C
3
photosynthetic pathway. To examine environmental
effects including the effect of increasing [CO
2
] on soybean growth and development is very
important, because plants develop and grow properly in proper conditions environmentally and
genetically.
A number of previous studies showed that elevated [CO
2
] affected photosynthetic behavior
of crops such as soybean. Many previous studies showed positive responses of soybean to
elevated [CO
2
] (Rogers et al. 1997; Kimball et al., 2002; Pritchard and Amthor, 2005; Alagarswamy
et al., 2006), but some other studies found down-regulation of photosynthesis under elevated [CO
2
]
(Sim et al. 1998; Sawada et al. 2001; Ainsworth et al. 2004; Kanemoto et al. 2009; Matsunami et al.
2009; Otera et al. 2011). The objective of the present study was to examine how the acclimation of
photosynthesis occurs in soybean under elevated [CO
2
].
Phenomenon of photosynthetic acclimation in plants can be ascribed to several factors.
Several previous studies reported that acclimation of photosynthesis occurred for different reasons.
Firstly, N limitation in leaves may cause photosynthetic acclimation (Kanemoto et al. 2009; Antal et
al. 2010). Secondly, starch accumulation in leaves reduced Rubisco activity and induced
photosynthetic acclimation (Sims et al. 1998; Sawada et al. 2001). Thirdly, balance in sink and
th
source affected photosynthetic acclimation (Rogers et al. 1998; Ainsworth et al. 2004). Fourthly,
decrease of chlorophyll content or Rubisco activity in leaves may affect photosynthetic acclimation
(Hotta et al. 1987; Sage et al. 1989). Finally, growth temperature induced photosynthetic
acclimation in some C
3
species (Yamori et al. 2005).


A soybean cultivar Enrei (normally nodulating) was used in this study. Four seeds per pot
(7 L) were sown on 6 June 2010 then thinned to one plant after emergence. Every pot was applied
6 g of compound fertilizer (N-P
2
O
5
-K
2
O: 5-15-20) and 10 g of garden lime. The amount of each
element per pot was N-0.3 g, P
2
O
5
-1.5 g, K
2
O-1.2 g and SiO
2
-2.8 g, Ca-0.4 g and Mg-0.4 g. The
seeds were inoculated with Bradyrhyzobium japonicum strain. The soil used was low-humic
Andosol type. The plants were grown in the temperature gradient chambers (Gradiotron) of National
Agricultural Research Center for Tohoku Region, Morioka, Japan, during June to October in 2010.
There were two levels of [CO
2
] inside the chamber: ambient (380 mol mol
-1
) and elevated (580
mol mol
-1
). The half of plants were transferred into the different [CO
2
] regime (from ambient to
elevated (A-E) or from elevated to ambient (E-A)) at flowering (48 DAS (R1)). The [CO
2
] and
temperature around plant canopy were monitored every half hour by sensors which were installed
above the plots.
Measurement of photosynthesis was conducted at 2 DAT and 35 DAT. Chlorophyll
fluorescence was determined by using portable photosynthesis system (LI-6400-40 with leaf
chamber fluorometer, LI-cor Inc., NE, USA). The air flow to the chamber was controlled at 500 mol
s
-1
. The measurements were conducted at saturated PPFD (1,500 mol m
-2
s
-1
). The photosynthetic
measurement was conducted at varying [CO
2
] with a range of 100 1,250 mol mol
-1
(A-Ci curve).
The values used for the calculation of ETR are as follows; maximal fluorescence (Fm
`
), steady-state
fluorescence (Fs) and photosystem II efficiency (PhiPS2) with equation
(

` m F
F m` F s
. ETR was
determined by the equation
(

` m F
F ` m F s
.[I
leaf
] ,

where f is fraction of absorbed quanta that is used by PSII, and is typically assumed to be 0.5 for C
3

plants, I is incident PPFD (1,500 mol m
-2
s
-1
),
leaf
is leaf absorptance which is assumed to be 0.85
(Genty et al. 1989). Measurements were conducted on the plants which were transferred (A-E, E-A)
and untransferred (A-A, E-E). Two to three plants for each plot were used for the measurements.


Under elevated [CO
2
], photosynthetic rate was markedly enhanced at the early growth
stage, whereas it was decreased at the later growth stage on both transferred and untransferred
plants (Fig. 1), indicating that the acclimation occurred at the later growth stage of the plants
regardless of the transfer. Electron transport rate (ETR) curve of the plants under elevated [CO
2
]
regime became plateau at about 300 mol mol
-1
intercellular [CO
2
] at the later growth stage (35
days after transfer (DAT)), which was less than the plateaued value under ambient [CO
2
] regime
(320 mol mol
-1
) (Fig. 2), indicating that acclimation of photosynthesis occurred at about 300 mol
mol
-1
intercellular [CO
2
] probably due to decreased RuBP regeneration (Sharkey et al., 2007) which
was affected by decrease in stomatal conductance (Fig. 3). Moreover, the leaf N and chlorophyll
content (SPAD reading) of the plants grown under elevated [CO
2
] regime was lower than those of
th
the plants grown under ambient [CO
2
] regime at the later growth stage (80 days after sowing
(DAS)/32 DAT) (data not shown).

Measurements were conducted at saturated PPFD (1,500 mol m
-2
s
-1
) under respective [CO
2
] (A and E). Vertical bars indicate
SE of three or five plants. *: significantly different at the 5% level between A and E [CO
2
] regimes.

Figure 1. Photosynthetic rates of transferred (AE, EA) and untransferred (A, E) plants at the early growth stages
(49, 54, and 80 DAS).

Fluorescence measurements were conducted at saturated PPFD (1,500 mol m
-2
s
-1
).

Figure 2. Photosynthetic rate and electron transport rate at 2 DAT and at 35 DAT of transferred (A-E, E-A) and
untransferred (A-A, E-E) plants.

Measurements were made in the morning at 80 DAS/32 DAT.

Figure 3. Effects of [CO
2
] (A, E) on stomatal conductance of leaves.
A AE E EA A AE E EA A AE E EA
S
t
o
m
a
t
a
l

c
o
n
d
u
c
t
a
n
c
e

(
m
o
l

m
-
2

s
-
1
)

A AE E EA
th
References
Ainsworth EA, Rogers A, Nelson R, Long SP (2004). Testing the sourcesink hypothesis of down-regulation
of ptosynthesis in elevated [CO
2
] in the field with single gene substitutions in Glycine max. Agricultural
and Forest Meteorology 122: 8594
Alagarswamy G, Boote KJ, Allen LH, Jr, Jones JW (2006). Evaluating the CROPGROsoybean model ability to
simulate photosynthesis response to carbon dioxide levels. Agronomy Journal 98: 3442.
Antal T, Mattila H, Yatkin MH, Tyystjrvi T, Tyystjrvi E (2010). Acclimation of photosynthesis to nitrogen
deficiency in Phaseolus vulgaris. Planta 232: 887-898
Genty B, Briantais JM, Baker NR (1989). The relationship between the quantum yield of photosynthetic electron
transport and quenching of chlorophyll fluorescence. Biochimica et Biophysica Acta 990: 87-92
Kanemoto K, Yamashita Y, Ozawa T, Manishi N, Nguyen NT, Suwa R, Mohapatra PK, Kanai S, Moghaieb RE,
Ito J, El-Shemy H, Fujita K (2009). Photosynthetic acclimation to elevated CO
2
is dependent on N
partitioning and transpiration in soybean. Plant Science 177: 398403
Kimball BA, Kobayashi K, Bindi M (2002). Responses of agricultural crops to free-air CO
2
enrichment. Advances
in Agronomy 77: 293-368
Matsunami T, Otera M, Amemiya S, Kokubun M, Okada M (2009). Effect of CO
2
concentration, temperature
and N fertilization on biomass production of soybean genotypes differing in N fixation capacity. Plant
Production Science 12: 156-167
Otera M, Kokubun M, Tabei H, Matsunami T, Maekawa T, Okada M (2011). Is yield enhancement by CO
2

enrichment greater in genotypes with a higher capacity for nitrogen fixation? Agricultural and Forest
Meteorology 151: 1385-1393
Pritchard SG, Amthor JS (2005). Crops and environmental change. Food Products Press, New York. pp. 1-421
Rogers A, Fischer BU, Bryant J, Frehner M, Blum H, Raines CA, Long SP (1998). Acclimation of photosynthesis
to elevated CO
2
under low-nitrogen nutrition is affected by the capacity for assimilate utilization.
Perennial ryegrass under free-air CO
2
enrichment. Plant Physiology 118: 683689
Rogers HH, Runion GB, Krupa SV, Prior SA (1997). Plant responses to atmospheric CO
2
enrichment:
implications in root-soil-microbe interactions. In Allen LH, et al. eds., Advances in carbon dioxide effects
research. ASA, CSSA, SSSA, Madison. pp. 1-34
Sage RF, Sharkey TD, Seemann JR (1989). Acclimation of photosynthesis to elevated CO
2
in five C
3
species.
Plant Physiology 89: 590-596
Sawada S, Kuninaka M, Watanabe K, Sato A, Kawamura H, Komine K, Sakamoto T, Kasai M (2001). The
mechanism to suppress photosynthesis through end-product inhibition in single-rooted soybean leaves
during acclimation to CO
2
enrichment. Plant and Cell Physiology 42: 1093-1102
Sharkey TD, Bernacchi CJ, Farquhar GD, Singsaas E (2007). Fitting photosynthetic carbon dioxide response
curves for C
3
leaves. Plant, Cell and Environment 30: 10351040
Sims DA, Luol Y, Seemann JR (1998). Comparison of photosynthetic acclimation to elevated CO
2
and limited
nitrogen supply in soybean. Plant, Cell and Environment 21:945952
Yamori W, Noguchi K, Terashima I (2005) Temperature acclimation of photosynthesis in spinach leaves:
analyses of photosynthetic components and temperature dependencies of photosynthetic partial
reactions. Plant, Cell and Environment 28: 536547

th
The Effect of Organic Materials and Decomposer on Soybean Growth
and Production

Sandra Arifin Aziz
a*
, Sri Ayu Dwi lestari
a

a
Bogor Agricultural University,
Department of Agronomy and Horticulture, Bogor Agricultural University, Bogor, Indonesia
* Corresponding author: Department of Agronomy and Horticulture, Bogor Agricultural University, Bogor,
Jl Meranti, Kampus Darmaga, Bogor, 16680, Indonesia
Tel.: +62 0251 8629353; fax: +62 0251 8629353
[email protected]

Abstract

Field experiment was set up in Cikarawang, Darmaga Bogor, Indonesia from December 2010 to April 2011. The
objective of the study was to investigate the effect of chicken manure, rice straw, and green manure of Tithonia
diversifolia with the application of decomposer, i.e. chicken manure liquid, chicken manure + Tithonia diversifolia
liquids, and biofertilizer under organic farming system. A randomized block design was laid out with organic
materials (chicken manure, rice straw and green manure of Tithonia diversifolia) as the first factor and
decomposers (chicken manure liquid, chicken manure + Tithonia diversifolia liquid, and biofertilizer) as the
second factor. The results showed that chicken manure gave the best effect on soybean growth and production.
Soybean productivities from organic treatment chicken manure, green manure of Tithonia diversifolia, and rice
straw were 1.00, 0.85, and 0.73 ton dry seed ha
-1
, respectively. Biofertilizer gave better response on soybean
growth and production components than chicken manure + Tithonia diversifolia liquid, chicken manure liquid and
control, i.e. 089, 088, 0.82, and 0.98 ton dry seed ha
-1
, respectively.

Keywords: organic soybean, decomposer, chicken manure, rice straw, Tithonia diversifolia Hemsl

Introduction

Increasing the inputs of nutrients has played a major role in increasing the supply of food
to a continually growing world population. However, focusing attention on the most important
nutrients, such as nitrogen (N), has in some cases led to nutrient imbalances, some excess
applications especially of N, inefficient use and large losses to the environment with impacts on air
and water quality, biodiversity and human health. In contrast, food exports from the developing to
the developed world are depleting soils of nutrients in some countries. Better management of all
essential nutrients is required that delivers sustainable agriculture and maintains the necessary
increases in food production while minimizing waste, economic loss and environmental impacts.
More extensive production systems typified by organic farming may prove to be sustainable.
However, for most of the developed world, and in the developing world where an ever-growing
population demands more food, it will be essential to increase the efficiency of nutrient use in
conventional systems (Gouldin et al., 2008).
The success of organic system in supporting national food security is still in doubt because
the production of organic farming system is generally less than that of conventional farming.
However, organic farming system may be able to support food security in local level because the
continuity of plant production is possible. Farmers can use on-farm inputs that normally are
available at production site and avoid the use of chemical fertilizer and pesticide which is relatively
expensive and negative impact to the environment.
Animal and green manure can be used as organic fertilizer for production of organic
vegetable soybean (Melati and Andriyani, 2005; Sinaga, 2005; Kurniasih, 2006). Chicken manure
gave better result than sheep manure (Sinaga, 2005), while Centrosema pubescens was better
th
than Calopogonium mucunoides and Crotalaria juncea (Sinaga, 2005; Kurniasih, 2006). Chicken
manure 10 ton ha
-1
increased the vegetative growth and production in organic soybean (Melati and
Andriyani, 2005).
In Indonesia, soybean is one of the crops used in the cropping pattern in the lowland. Arafah
and Sirappa (2003) stated that rice straw should be incorporated to the soil after every harvest so it
can be beneficial to the next crop in the cropping pattern. Indriani (2000) found that Tithonia
diversifolia contains high nutrients, especially Nitrogen. This nitrogen can be useful in assisting
decomposting bacteria in decomposition process.
One of the obstacles in organic agriculture is the decomposition process of the organic
matter in the soil. Local microorganisms from various organic matters (fruits, plants, fish bones,
dead animal and garbage) around us can be used as media for microorganism for decomposition
process (Indriani, 2000). This effort can be used to optimize the growth and activity of the
microorganism that decomposed the organic matter (Sutaryono dan Fauzi, 2007). Combination of
biofertilizer and various organic matters influenced the physical and biological soil properties
(Mezuan et al., 2002). Bertham (2002) studied biofertilizer application that showed the increasing
total pod number, filled pod number, and root nodule number in soybean. Further Hindratno (2006)
found that decomposer application or chicken manure liquid as decomposer increased the plant
height and fresh pod of vegetable soybean weight than without decomposer application.
This research was aimed to study the influence of organic matter, i.e. chicken manure, rice
straw, and Tithonia diversifolia with decomposer, i.e. chicken manure liquid, chicken
manure+Tithonia diversifolia, and biofertilizer (Bioextrim) to the organic soybean production.


The research was carried out at organic research station Cikarawang, Bogor, West Java,
Indonesia, from November 2010 to April 2011. A randomized block design was laid out with organic
materials (i.e. chicken manure, rice straw, and green manure of Tithonia diversifolia) as the first
factor and decomposers (i.e. chicken manure liquid, chicken manure + Tithonia diversifolia liquid,
and biofertilizer Bioextrim) as the second factor. Duncans Multiple Range Test (DMRT) with =5%
and t-Dunnet test for comparison between treatments with control (rice straw without dekomposer)
were used in this experiment.
Liming with 2 tonnes dolomit ha
-1
and 2 ton ash ricehull ha
-1
were given in row for soil
conditioning 4 Weeks Before Planting (-4 WAP/Weeks After Planting). Organic matter as treatments
were given in the form of 10 tonnes chicken manure ha
-1
, 10 ton rice straw ha
-1
, and 10 tonnes of
Tithonia diversifolia ha
-1
and decomposer in the form of chicken manure liquid, chicken manure +
Tithonia diversifolia liquid, and biofertilizer. Coconut water and red sugar, i.e. 40 l and 4 kg, were
used as the solution for each type of decomposer liquid and then fermented for 6 weeks (at -6
WAP) and given as soil drench.
Cymbopogon nardus and Tagetes erecta L. were used as the repellent plant (Kusheryani
and Aziz, 2005). Extract of Cymbopogon nardus, Cymbopogon nardus + Tithonia diversifolia, and
neem (Azadirachta indica A. Juss) were used as organic pest control and sprayed every week.
Soybean of Wilis variety were planted 25 x 10 cm with the repellent plant in the middle of every plot.


The soil analysis before the experiment showed pH at 5.7 (slightly acid), C-organic at
1.20% (high), total N at 2.2 ppm (low), CEC low, base saturity of 29.26% (medium). Clay in texture
(sand, loam and sand, i.e. 6.93, 23.26 and 69.81%, respectively). After the treatment the pH on
control, Tithonia diversifolia and biofertilizer were 5.7 (slightly acid). On rice straw and chicken
th
manure liquid, and rice straw and biofertilizer the pH increased to 6.50, whereas the other six
treatments were neutral to base (6.60-7.30). Low total nitrogen (0.12-0.22%), high C-organic was
1.20-2.39%, P availability was 2.80-10.20 ppm, low to high K at 0.29-0.94 me/100g, high base
saturity was 64.04-96.15%.
Penta and tetra-foliate leaves found on 7 WAP, mostly on Tithonia diversifolia plots, with
dark green colour, broad leaves and thicker canopy. On 5 WAP Pseudomonas syringae pv.
glycinea were found on every plant. Saleh and Hardaningsih (2007) stated that this disease was
mostly found in high altitude in Indonesia, with wet weather and high temperature.
Organic matter significantly affected seed growth percentage at 2 WAP, number of
branches on 3, 5, 7, 9, 11, 13 WAP; number of tetra and penta-foliate on 7 WAP; shoot, root,
nodule wet and dry weight on 7 WAP, disease prevalence on 8 WAP; insect infestation on 8 and 10
WAP; number of empty pod on 13 WAP; number of plant harvested; dry seed weight per 7.5 m
2
;
and soybean productivity (Table 1).

Table1. Organic matter on vegetative and generative variables

Variables WAP
Organic Matter
Control
Chicken Manure Rice Straw Tithonia diversifolia
Growth percentage 2 336.33 b 369.22 ab 386.11 a 382.33

Plant height (cm) 13 12.79

12.88

13.53

12.59

Number of branches 11 51.06

52.22

49.76

49.85

Number of productive branches 13 3.17 a+ 2.90 b+ 2.83 b+ 2.47

Leaf number 3 8.73 a+ 6.69 bc 7.26 b 6.37

11 10.54 a+ 9.24 ab 8.43 b 8.63

Tetrafoliate 7 10.33 a+ 9.12 ab 8.30 b 8.53

Pentafoliate 7 10.24 a+ 9.06 ab 8.13 b 8.40

NAR (g/cm
2
/weeks) 5-7 9.79 a 8.82 ab 7.94 b 8.27

7-9 2.77

2.75

2.78 + 2.60

RGR (g/weeks) 5-7 6.59

5.92

6.07

6.00

7-9 12.38

11.49

11.51

11.63

Nodule wet weight (g) 7 135.11 a+ 77.33 c+ 87.78 b+ 68.00

Shoot dry weight (g) 7 37.11 a+ 17.78 c+ 24.56 b+ 8.67

Leaf water content (%) 7 0.34

0.15

0.28

0.05

Insect infestation (%) 10 5.07 b 3.73 b 7.53 a+ 4.70

Disease prevalence (%) 8 0.74 b+ 0.51 c 1.03 a+ 0.52

Number of filled pod

24.14

19.10

21.43

19.50

Number of empty pod

3.16 a+ 1.74 ab 2.72 a 1.07

Seed dry weight (g)

46.69

33.28

40.36

36.58

Number of plants harvested

217.11 b 241.00 ab 249.89 a 255.33

100 seed dry weight (g)

9.59

9.15

8.98

8.65

Seed dry weight /7.5 m
2
(g)

752.44 a 550.67 b 636.78 ab 738.33

Productivity (ton/ha)

1.00 a 0.73 b 0.85 ab 0.98

Numbers followed by different letters in the same row significantly different at 5 and 1 % DMRT test; figures followed by (+) in
the same row significantly different at 5% Dunnet test with the control.
th
Decomposer significantly affected number of branches on 3, 5 WAP; number of tetra and
penta foliate on 7 WAP; Nett Assimilation Rate (NAR) on 7-9 WAP; shoot and root wet weight on 7
WAP; shoot dry weight on 7 WAP; disease prevalence on 8 WAP; and insect infestation on 8 WAP
(Table 2). Combination of organic matter and decomposer significantly affected Nett Assimilation
Rate on 7-9 WAP; shoot and root wet weight on 7 WAP; shoot and root dry weight on 7 WAP; and
insect infestation on 10 WAP.

Table2. Decomposer on vegetative and generative variables

Variables WAP
Decomposer
Control
Chicken Manure
Liquid
Chicken manure
+ Tithonia
diversifolia liquid
Biofertilizer
Growth percentage 2 357.67 372.33 361.67 382.33

Plant height (cm) 13 50.83

51.29

50.93

49.85

Number of branches 3 3.04 a+ 3.01 a+ 2.85 b+ 2.47

5 7.8 + 7.6 + 7.3

6.4

11 9.3

9.5

8.6

8.4
Number of productive
branches 13 8.9

9.2

8.5

8.3

Leaf number 3 2.8

2.8 + 2.7

2.6

11 11.3

10.7

9.6

10.1

Tetrafoliate 7 102.1 a+ 100.1 ab+ 98 b+ 68

Pentafoliate 7 27.7 a+ 26.3 ab+ 25.1 b+ 8.7

NAR (g/cm
2
/weeks) 5-7 2.5x10
-3

1.9x10
-3

2.4x10
-3

4.5x10
-4

7-9 2.8x10
-3
a 1x10
-3
b 7.6x10
-4
b 1x10
-3

RGR (g/weeks) 5-7 0.26

0.23

0.29

0.05

7-9 0.18

0.1

0.07

0.12

Shoot wet weight (g) 7 4.6 b 5.16 b 6.63 a+ 4.7

Root wet weight (g) 7 0.65 bc 0.7 b 0.93 a 0.52

Shoot dry weight (g) 7 1.34 b 1.36 b 1.94 a 1.41

Nodule dry weight (g) 7 0.03

0.03

0.04 + 9x10
-3

Insect infestation (%) 8 20.89 a+ 19.47 b+ 21.98 a+ 29.16

10 6.89

7.69

7.67

5.48

Disease prevalence (%) 8 69.16 ab+ 68.29 b+ 69.65 a+ 79.46

Seed dry weight (g)

41.49

40.3

38.54

36.58

Number of plants harvested

231.8

239.6

236.7

255.3

100 seed dry weight (g)

9.18

9.39

9.15

8.65

Seed dry weight /7.5 m
2
(g)

658

615.67

666.22

738.33

Productivity (ton/ha) 0.88 0.82 0.89 0.98
Numbers followed by different letters in the same row significantly different at 5 and 1 % DMRT test; figures followed by (+) in
the same row significantly different at 5% Dunnet test with the control

The higher result on control plots seemed to be affected by the plot placement in the field
that supplied more water in the beginning of the experiment than the treatment plots. Soil in the
treatment plots were hard because of the changed condition from paddy field to the rain-fed
th
condition for the soybean planting. All the organic manure was recommended for soybean planting
after paddy field. There was no need to apply decomposer after the paddy field for soybean planting
with rice straw incorporation to the soil.

References

Arafah and MP Sirappa. 2003. Kajian penggunaan jerami dan pupuk N, P, dan K pada lahan sawah irigasi. J.
Ilmu Tanah dan Lingkungan 4(1):15-24.
Bertham YH. 2002. Potensi pupuk hayati dalam peningkatan produktivitas kacang tanah dan kedelai pada
tanah seri Kandanglimun, Bengkulu. JIPI. 4(1):18-26.
Gouldin K, S Jarvis, A Whitmore. 2008. Optimizing nutrient management for farm systems. Phil. Trans. R. Soc.
B 363:667-680. doi: 10.1098/rstb.2007.2177.
Hindratno TP. 2006. Pengaruh Lama Dekomposisi Pupuk Hijau dan Jenis Pelapuk terhadap Budi Daya Kedelai
(Glycine max (L.) Merrill) Panen Muda Secara Organik. Skripsi. Program Studi Agronomi, Fakultas
Pertanian, Institut Pertanian Bogor. 50 hal.
Indriani YH. 2000. Membuat kompos secara kilat. Penebar Swadaya. Jakarta. 62 hal.
Kusheryani I dan SA Aziz. 2005. Pengaruh Jenis Tanaman Penolak Organisme Pengganggu Tanaman
terhadap Pertumbuhan dan Produksi Tanaman Kedelai (Glycine max (L.) Merrill) yang Diusahakan Secara
Organik. Bul. Agron. 34(1):39-45.
Kurniasih W. 2006. Pengaruh Jenis, Dosis Benih dan Umur Tanaman Pupuk Hijau terhadap Produksi Kedelai
(Glycine max (L.) Merrill) Panen Muda. Skripsi. Program Studi Agronomi, Fakultas Pertanian, Institut
Pertanian Bogor. Bogor. 65 hal.
Melati M dan W Andriyani. 2005. Pengaruh Pupuk Kandang Ayam dan Pupuk Hijau Calopogonium mucunoides
terhadap Pertumbuhan dan Produksi Kedelai Panen Muda yang Dibudidayakan Secara Organik. Bul.
Agron. 33(2):8-15.
Mezuan, IP Handayani, E Inoriah. 2002. Penerapan formulasi pupuk hayati untuk budidaya padi gogo : studi
rumah kaca. JIPI. 4(1):27-34.
Sinaga, YAS. 2005. Pengaruh Pemberian Pupuk Organik terhadap Pertumbuhan dan Produksi Kedelai
(Glycine max (L.) Merr) Panen Muda yang Diusahakan secara Organik. Skripsi. Program Studi Agronomi,
Fakultas Pertanian, Institut Pertanian Bogor. Bogor. 35 hal.
Sutaryono, YA dan MT. Fauzi. 2007. Potensi mikroorganisme lokal dalam memacu proses pengomposan padi.
J. Agroland 14(2):134-139.

th
Yield and Dry Matter Production of Japanese and US Soybean Cultivars
under Drought Stress

Yohei Kawasaki
a*
, Yu Tanaka
b
, Keisuke Katsura
a
a

a
Graduate School of Agriculture, Kyoto University, Japan
b
Graduate School of Science, Kyoto University, Japan
Tel.: +81 75 753 6042; Fax: +81 75 753 6065.
[email protected]

Abstract

The difference in soybean yield between Japan and US is enlarging. The authors reported that the higher yields
of US cultivars than Japanese cultivars were attributed to greater dry matter production and radiation use
efficiency and that the US cultivars tended to have higher leaf stomatal conductance to water vapor (gs). These
traits may cause different sensitivity to drought between cultivars. The objective of this study was to examine
whether the yield response to drought differed between a Japanese cv. Tachinagaha (Tc) and a US cv. UA-4805
(UA) with low and high leaf gs, respectively. The two cultivars were grown on a drained paddy field in the Exp.
Farm of Kyoto Univ. (Takatsuki, Japan) and the treatment with irrigation (Control) and without irrigation
(Drought) was started at 20 days after emergence. The volumetric soil water content was on average 6% lower
in the Drought than in the control plots. The leaf area development was inhibited only in UA under Drought. The
gs was higher in UA than in Tc and it decreased in both cultivars by 34~38%. UA showed a greater mean seed
yield and harvest index. Drought reduced mean seed yield and total dry weight of two cultivars. The yield
reduction by drought in UA was associated with reduced radiation intercepted, while yield reduction in Tc was
associated with reduced radiation use efficiency and harvest index. The significant GE interaction was detected
in harvest index and mean fraction of radiation intercepted. The two cultivars did not differ in yield response to
drought, but they differed in the yield components affected by drought.

Keywords: soybean (Glycine max (L.) Merrill), yield, genotype by environment interaction, drought

Introduction

The difference in soybean yield between Japan and US is enlarging. The authors reported
that the higher yields of US cultivars than Japanese cultivars were attributed to greater dry matter
production and radiation use efficiency (Kawasaki et al. 2010) and that the US cultivars tended to
have higher leaf stomatal conductance to water vapor (gs) (Tanaka et al. 2010). These traits may
cause different sensitivity to drought between cultivars. The objective of this study was to examine
whether the yield response to drought differed between a Japanese cv. Tachinagaha (Tc) and a US
cv. UA-4805 (UA) with low and high leaf gs, respectively.


The two cultivars were grown on a drained paddy field in the Experimental Farm of Kyoto
University (Takatsuki, Japan, Eutric Fluvisols) located at 3451N and 13537E. The date of sowing
was 7
th
of July 2010 and the date of emergence was 12
nd
of July. Plant spacing was 0.7 by 0.15m.
Fertilizers of N, P
2
O
5
, K
2
O were incorporated into the soil before sowing at 3, 10 and 10 gm
-2
,
respectively.
The treatment with irrigation (Control) and without irrigation (Drought) was started at 20
days after emergence. In the Control, irrigation water was evenly applied using the plastic tube
th
(Sumisansui, Sumika Agrotech Co. Ltd.) extended on the ground in every other interrow. Irrigation
was conducted when the soil matric potential declined lower than 50kPa. The volumetric soil water
content was measured twice a week using EC-5 (Decagon Devices, Inc.).
The canopy coverage was measured by the digital image analysis using ImageJ (NIH,
USA) (Purcell 2000, Shiraiwa et al. 2011). The total above-ground plant part was harvested at 35,
47, 61, and 74 days after emergence from a 1.26 m
2
land area and the dry matter weight was
determined after drying at 80C for 72h. The Leaf Area Index (LAI) was estimated by measuring leaf
area of representative plants.


The volumetric soil water content was on average of 6% lower in the Drought than in the
Control plots (Figure 1). The leaf area development was inhibited only in UA under Drought (Figures
2 and 3). The gs was higher in UA than in Tc and it decreased in both cultivars by 34~38% (Figures
4 and 5).

Figure 1. Change in volumetric soil water content measured by EC-5 (Decagon Devices, Inc.).

Figure 2. Change in canopy coverage measured by digital image analysis.

th

Figure 3. Change in Leaf Area Index.

Figure 4. Stomatal conductance of Tachinagaha and UA-4805 under different soil conditions.

Figure 5. Change in total above ground dry weight.

UA showed a greater mean seed yield and harvest index in both of Control and Drought.
Drought reduced mean seed yield and total dry weight of two cultivars. The yield reduction by
drought in UA was associated with reduced radiation intercepted, while yield reduction in Tc was
associated with reduced radiation use efficiency and harvest index. The significant GE interaction
was detected in harvest index and mean fraction of radiation intercepted (Table 1).
These results indicated that the two cultivars did not differ in yield response to drought, but
they differed in the yield components affected by drought.

th
Table 1. Yield and yield components of drought experiment at Takatsuki in 2010

Seed
yield
(t ha
-1
)
Total
Dry
Weight
(t ha
-1
)
HI Radiation
Use
Efficiency
(g MJ
-2
)
Mean F
(%)
Total radiation
intercepted
(MJ)
Total
incident
radiation
(MJ)
Tachinagaha control 3.77 6.22 0.521 0.504 72.9 1233 1690
Tachinagaha drought 2.17 5.34 0.341 0.455 69.2 1170 1691
UA-4805 control 4.84 7.12 0.585 0.581 71.7 1225 1708
UA-4805 drought 3.65 5.74 0.531 0.572 58.6 1000 1705

Analisis of varience

Cultivar 29.75 ** 19.65 * 27.49 ** 46.75 ** 13.87 * 8.84 *
Treatment 35.49 ** 58.79 ** 32.50 ** 4.16 * 28.33 ** 23.13 **
cultivar x treatment 0.77 NS 2.98 NS 8.14 * 198 NS 8.72 * 7.33 NS

References

Kawasaki Y, Tanaka Y, Katsura K, Purcell LC, Homma K, Katsube-Tanaka T, Shiraiwa T. 2010. Yield and Dry
Matter Productivity of Japanese and US Soybean CultivarsA Comparison in the Warm Regions.
Jpn. J. Crop Sci. 79(S2):102-103.
Tanaka Y, Fujii K, Shiraiwa T. 2010. Variability of Leaf Morphology and Stomatal Conductance in Soybean
[Glycine max (L.) Merr.] Cultivars. Crop Sci. 50:2525-2532.
Purcell LC. 2000. Soybean canopy coverage and light interception measurements using digital imagery. Crop
Sci. 40:834-837.
Shiraiwa T, Kawasaki Y, Homma K. 2010. Estimation of Crop Radiation Use Efficiency. Jpn. J. Crop Sci. 80:360-
364.

th
Selection of F4, F5 and F6 Soybean Breeding Lines for High Yield
and Large Seed Size

Darman M. Arsyad
a
*, Asadi
b

a
Central Institute for Agricultural Technology Assessment and Development, Bogor, Indonesia
b
Research Institute for Agricultural Biotechnology and Agricultural Genetic Resources, Bogor, Indonesia
* Corresponding author: Central Institute for Agricultural Technology Assessment and Development,
Bogor, Indonesia
Tel.: +62-251-8351277; Fax: +62-251-8350928
[email protected]

Abstract

The first step in a cultivar development is to form a population with genetic variability for the characters of
interest. This is done by hybridization of genetically different parents. Hybridization was made to combine the
characters of high yield potential, wide adaptability, desirable agronomic characters, and large seed size by
using cv. Tanggamus, Sibayak, Argomulyo, Anjasmoro, Panderman and Local Tegal. Amount of 4800 F4 lines
originated from five single cross combination were planted in rice field, Sukawening, Garut District, West Java
on early dry season 2007. Pedigree method of selection was used. Each line was grown in one row of three
meters length and 40 cm between rows. There was a high variability on agronomic characters (plant height, pod
number, seed yield and seed size). Amount 1311 F5 lines were selected and grown in the same location on late
dry season 2007. Amount of 540 F6 lines were selected and grown in the same location on early rainy season
2007/2008. Sixty-two F7 lines were selected, and 42 lines among them had high yield and large seed size.

Keywords: high yield, large seed size, soybean breeding lines

Introduction

Breeding for high yield potential is generally the major goal in any breeding program
including soybean. Breeding for high yield potential is inextricably linked with breeding for other
characteristics. Today the preferences of users (farmers and craftsmen tempeh and tofu) were
more likely to require large varieties of soybean seed. Craftsmen tempeh and tofu have long
accustomed to using large seed soybean imports, so that preferences are now a lot towards the
large seed.
To meet user demand, then breeding programs to produce varieties of soybean large seed
in major need of attention. A number of varieties of large seed soybean have been available such
as Argomulyo, Burangrang, Anjasmoro, and Grobogan (Hermanto et al., 2009).
As an effort to produce new varieties of soybeans that are superior to the existing varieties,
a number of crossing (hybridization) between soybean genotypes of high yield potential, quite broad
adaptability, many pods and smaller seed size with the genotypes of relatively low yield potential,
narrow adaptability, few pods, and large seed size, and were carried out in 2004 (Arsyad et al.
2005).
This study aimed to: (a) obtain expected breeding lines better than the existing varieties,
which possess higher yield potential, desirable agronomic traits and has a large or slightly larger
seed size, and (b) study the behavior of the relationship among traits in soybean.


Plant Materials
Selection of F4, F5 and F6 soybean breeding lines was conducted in the rice field of
Sukasono Village, Sukawening Subdistrict, Garut District, at the growing season I (April-June 2007),
season II (July-September 2007) and the season III (September-November 2007), respectively.
Selection materials that were used in the firs selection In the season I the 4800 F4 soybean
breeding lines were grown and selected. Those breeding lines were derived from a combination of
five single crosses, which were Tanggamus x Tegal, Tanggamus x Anjasmoro, Sibayak x Tegal,
Sibayak x Argomulyo, and Sibayak x Panderman, made in 2005 (Arsyad et al. 2005). In season II,
th
the 1311 F5 breeding lines wich were selected from the F4 lines in season I, were grown and then
as many as 540 F6 lines were selected. Those 540 F6 lines were grown in season III.

Methods

Pedigree method based selection was used in each generation (Fehr, 1987). In each
season, each breeding lines was grown as a single row with 1.5 meters length. Spacing between
rows (lines) were 40 cm and 10 cm within rows, and one seed/hole. Intensive techniques cultivation
involves fertilizing with 75 kg urea, 200 kg SP36, and 150 kg KCl per ha, controlling of weeds,
pests and diseases were carried out. Irrigation was applied, if there is no rain. The selection criteria
was an ideal plant type,i.e. sturdy plants (not fall), plant height > 70 cm with 4-5 branches, medium
leaf size, determinate type, more than 70 pods/plant and large pods. Selection procedure was done
as follows: First, selected the good rows of plants, and secondly, selected the 3-5 plants in selected
row that meet the selection criteria. Each selected individual plant was a new breeding line to the
next generation. Data analysis was done by creating the frequency distribution of selected breeding
lines, calculate the mean and standard deviation for the observed characters of each population, as
well as t test for mean population comparation (Gomez & Gomez 1984, Sugiyono 2009).


Selection of F4 Lines
Before time to harvest, around 1600 lines was selected and then as many as 1311 lines
was selected based on yield and seed quality. Only breeding lines derived from three crossing
combinations were selected. Those were the crosses between Sibayak x Tegal (Code V),
Tanggamus x Tegal (Code U) and Sibayak x Argomulyo (Code W). The other two crosses
(Tanggamus x Anjasmoro and Sibayak x Panderman) derived inferior progenies. .
Frequency distribution of selected breeding lines based on crop yield are presented in
Figures 1. The range of lines seem still very wide, ranging from less than 10 g to more than 50
g/line, with the highest frequency was in the range of 21-25 g/line. Genotype of parents produuced
average yield of less than 20 g/genotype. This indicated the presence of transgressive segregation
on the breeding materials. Variability was also found in the seed size (100 seed weight), plant
height, and number of pods (Figure 2-4). The selection would be effective when there was wide
phenotypic variability among breeding lines. This was understandable because the selected lines
were still at F4 generation and was not selected since F2. The frequency of heterozygous
individuals at a locus was 50% in F2 (Fehr 1983), and because the selection has not been done
since the F2, therefore the heterozygote frequency in the F4 was still high (50%).
Breeding lines derived from Sibayak x Tegal cross have an average higher yields, larger
seed, higher plant, but the number of pods is less than the breeding lines derived from Tanggamus
x Tegal and Sibayak x Argomulyo (Table 1). No yield different between breeding lines derived from
Tanggamus x Tegal and Sibayak x Argomulyo. Breeding lines derived from Sibayak x Tegal has
larger seed size compared to the breeding lines derived from Tanggamus x Tegal and Sibayak x
Argomulyo. Breeding lines derived from Sibayak x Argomulyo had a relatively smaller seed size
compared to the other two cross combinations, but it had more pods per plant. It appears a
tendency that the breeding lines of a large seed pods had fewer seeds, while breeding lines of
moderate or relatively small seed pods had more seeds.
A total of 203 breeding lines have been identified with high yield capacity, which was more
than 30 g/line (data not presented). A total of 99 breeding lines of which had large seed size
(>13g/100 seeds), and the other 104 breeding lines had moderate or relatively smaller seed size.
Selection will change the frequency of genotype and phenotype of a locus (Ferhr 1983). The basis
of the expected effect of the selection is the change of gene frequencies (Falconer, 1967), but we
do not know what the frequency of genes that changed, because the selection was only based on
phenotypic selection. The selection would be effective to choose recessive alleles, as consequently
in one generation all dominant alleles will be eliminated in the population. However, if the selection
is intended to eliminate the recessive alleles, it would be more difficult because it is covered by
dominant alleles in the heterozygous individuals (Fehr, 1983).
th
Although the selection in this study was only based on phenotypic values, it was expected
to be quite effective to gain the best selected lines, which is expected to produce good progenies.
The progress of the selection is determined by phenotypic variability, heritability values and
selection intensity (Falconer, 1967). Agronomic characters such as plant height, number of
branches and number of pods support high capacity of selected the breeding line.

Figure 1. Frequency distribution of F4 soybean breeding
lines for yield (g/plant), Garut, season I 2007.
Figure 2. Frequency distribution of F4 soybean
breeding lines for 100 seed weight (g),
Garut, season I 2007.

lines for plant height (cm), Garut, season I
2007.
breeding lines for pod number per plant,
Garut, season I 2007.

Table 1. Mean and standar deviation of seed yield, 100 seed weight, plant height, and number of pods per plant
of F4 lines originated of three single cross in rice field at Sukasono Village, Sukawening Subdistrict,
Garut District, early dry season of 2007

Population Number
of lines
Seed yield
(g)
100 seed
weight (g)
Plant height
(cm)
Number of pods
/ plant
V (Sibayak x Tegal) 490 24a 7.1 14.1a 2.1 58a 9.2 97b 25.4
U (Tanggamus x Tegal) 400 22b 6.8 12.6b 1.9 51b 8.1 100b 24.4
W (Sibayak x Argomulyo) 401 22b 7.3 10.9b 2.2 56a 7.6 124a 29.5
Value in the same column followed by the same letter are not different at 0.01 probability level


Before time to harvest around 700 lines was selected and, as many as 540 lines was
selected based on yield and seed quality. Frequency distribution of breeding lines on several
classes of seed yield is presented in Figure 5. The yield range of the breeding lines seemed quite
wide, ranging from less than 10 g to more than 30 g/line, with the highest frequency present in the
range of 11-15 g/line. The parent produced an average yield of less than 11g. A total of 191
th
breeding lines produced higher yield than that of the best parent (Tanggamus). This indicated the
presence of the transgressive segregation, i.e. breeding line yields were higher than that of both
parents. The occurence also the same as the seed size (100 seed weight), which was as many as
88 breeding lines contained a rather large to large seed size (Figures 6). Plant height and number
of pods showed a fairly high variability (Figure 7 and 8).
Breeding lines derived from Sibayak x Argomulyo had the higher average yields, higher
plant height, and more pods per plant than those of the breeding lines derived from Tanggamus x
Tegal and Sibayak x Tegal (Table 2). In contrast, breeding lines derived from Sibayak x Tegal
produced average seed size larger than that of the breeding lines derived from Tanggamus x Tegal
and Sibayak x Argomulyo. It was a tendency that the breeding lines of larger seed correlated with
fewer pods, shorter plants and lower grain yield. The selection would be effective when the high
variability occurred among breeding lines. A total of 62 breeding lines had high yield capacity (Table
3).

breeding lines for yield (g/plant), Garut,
season II 2007.
breeding lines for 100 seed weight (g),
Garut, season II 2007.

lines for plant height (cm), Garut, season II
2007.
breeding lines for pod number per plant,
Garut, season II 2007.


Of the 540 F6 breeding lines that were selected in the experiment on season III 2007, 100
breeding lines were selected at the harvesting time, and the best 60 breeding lines were selected
after processing. Of the 60 F7 breeding lines, as many as 42 breeding lines had the high yield
capacity and relatively large seed (Table 4). Among the 42 breeding lines, 16 breeding lines were
derived from the cross between Sibayak x Tegal, six breeding lines were derived from the cross
between Tanggamus x Tegal, and 20 breeding lines were derived from teh cross between Sibayak
x Argomulyo cross. Those breeding lines will be tested further in the preliminary yield testing on
early dry season of 2008.

th
Table 2. Mean and standar deviation of seed yield, 100 seed weight, plant height, and number of pods per plant
of F5 lines originated of three single cross in ricefield at Sukasono Village, Sukawening Subdistrict,
Garut District, late dry season of 2007

Population Number
of lines
Seed yield
(g)
100 seed
weight (g)
Plant height
(cm)
Number of
pods / plant
V (Sibayak x Tegal) 200 14b 4.9 11.1a 1.5 64b 12.3 79b 25.5
U (Tanggamus x Tegal) 200 12b 4.1 10.8b 1.5 50c 7.8 79b 22.8
W (Sibayak x Argomulyo) 140 18a 4.6 9.9b 1.5 68a 8.7 119a 27.2
Value in the same column followed by the same letter are not different at 0.01 probability level

Table 3. Performance of the best 62 F5 breeding lines in ricefield at Sukasono Village, Sukawening Subdistrict,
Garut District, season II 2007

Breeding line
Number
of lines
Plant
height
(cm)
Number of
branches
per plant
Number of
pods per
plant
Seed yield
(g)
100 seed
weight (g)
V (Sibayak x Tegal) 20 62
(46-100)
6.8
(4-10)
107
(77-240)
23.3
(21.2-26.4)
11.7
(9.9-14.9)
U (Tanggamus x Tegal) 11 53
(40-61)
6.9
(4-10)
111
(75-145)
21.8
(20.6-23.4)
10.9
(8.4-13.3)
W (Tanggamus x
Argomulyo)
31 69
(57-102)
6.5
(4-8)
148
(109-239)
23.8
(20.2-35.1)
13.0
(8.8-17.40
Tanggamus - 50 5 68 10.7 9.2
Sibayak - 56 5 86 10.0 9.8
Tegal - 39 2 27 4.4 17.2
Argomulyo - 40 5 52 8.9 13.3
Value in parenthese is a range

Table 4. Agronomic performance and seed yield of 42 F6 soybean breeding lines selected in ricefield at
Sukasono Village, Sukawening Subdistrict, Garut District, season III 2007

No. Breeding line Plant height
(cm)
Number of
branches
Number of
pods
Seed yield
(g)
100 seed weight
(g)
1 V-5-1-1-2 69 5 99 25.1 14.9
2 V-43-2-2-1 95 4 77 22.1 14.9
3 V-63-2-1-1 68 7 102 26.2 13.9
4 V-75-2-1-2 69 6 114 27.7 14.7
5 V-75-2-3-1 68 4 85 25.4 14.8
6 V-75-2-4-2 65 4 91 23.0 13.0
7 V-250-2-2-1 66 7 106 26.7 13.3
8 V-257-1-1-1 62 9 123 26.4 14.4
9 V-273-1-1-2 70 7 114 25.7 13.0
10 V-284-2-1-1 66 8 117 25.4 13.8
11 V-215-1-1-1 62 9 113 22.1 14.3
12 V-215-1-2-1 62 7 240 30.3 13.4
13 V-215-1-4-1 58 8 118 25.4 14.3
14 V-390-2-3-2 59 7 120 24.8 13.1
15 V-424-1-1-2 60 10 104 25.3 13.3
16 V-612-2-1-2 66 7 110 23.5 13.6
17 U-574-1-1-1 64 8 104 20.8 13.3
18 U-445-2-1-1 60 7 122 22.1 14.5
19 U-79-2-2-2 58 5 123 20.6 12.5
20 U-675-1-1-1 56 8 93 21.3 12.2
21 U-534-2-2-1 62 4 106 22.3 12.9
22 U-697-1-1-1 54 7 99 21.5 13.4
23 W-209-1-1-2 68 8 170 20.8 13.1
24 W-455-1-2-1 98 6 120 22.4 15.4
25 W-460-1-1-1 70 5 109 21.3 13.6
26 W-47-2-1-1 68 6 130 20.3 13.0
27 W-466-1-1-1 70 7 191 32.2 13.1
28 W-40-1-1-2 67 7 147 27.6 14.3
29 W-40-1-2-2 65 8 127 24.0 13.3
th
No. Breeding line Plant height
(cm)
Number of
branches
Number of
pods
Seed yield
(g)
100 seed weight
(g)
30 W-165-1-1-1 75 7 168 25.7 13.7
31 W-284-1-3-1 72 8 239 34.3 13.4
32 W-537-1-1-1 67 4 103 21.2 13.6
33 W-267-2-1-2 74 5 100 20.0 14.5
34 W-530-1-2-1 67 6 145 25.3 13.3
35 W-308-2-1-2 71 7 180 35.1 13.3
36 W-258-1-1-1 86 5 127 24.0 13.9
37 W-271-1-1-1 70 8 158 21.1 12.6
38 W-519-1-2-1 79 8 175 25.1 13.1
39 W-169-1-2-1 68 6 160 30.8 12.7
40 W-304-1-2-1 64 7 138 22.3 12.5
41 W-304-1-3-1 66 7 176 21.2 13.3
42 W-197-1-1-2 59 6 142 23.3 13.8
43 Tanggamus 58 6 68 10.7 10.2
44 Sibayak 60 6 86 10.0 11.1
45 Tegal 45 3 36 14.2 17.0
46 Argomulyo 54 5 58 18.5 14.6
V (16 lines) 67
(58-95)
6,8
(4-10)
114
(77-240)
25.3
(22.1-30.3)
13.9
(13.0-14.9)
U (6 lines) 59
(54-64)
6,5
(4-8)
108
(93-123)
21.4
(20.6-22.3)
13.1
(12.2-14.5)
W (20 lines) 71
(59-98)
6,5
(4-8)
150
(100-239)
24.9
(20.0-35.1)
13.5
(12.5-15.4)
Check (4 var.) 54
(45-60)
5
(3-6)
62
(36-86)
13.4
(10.0-18.5)
13.2
(10.2-17.0)
V= Sibayak x Tegal cross
U= Tanggamus x Tegal cross
W=Sibayak x Argomulyo cross
Value in parenthese is a range

Acknowledgment

The authors acknowledge the support of the Indonesian Ministry of Research and Technology, who
provided the funding for this research.

References

Arsyad DM, H Kuswantoro and Purwantoro. 2005. Hybridization, and selection penggaluran soybeans.
Technical Report Research Institute for Crop Legumes and Tuber (In Indonesian).
Burton JW. 1983. Quantitative genetics: Results relevant to soybean breeding, p. 211-248. In JR Wilcox (Ed.):
Soybean: Improvement, Production, and Uses. Second Edition, ASA, Wisconsin, No. 16 in series.
Falconer DS. 1967. Introduction to Quantitative Genetics.Robert MacLehose and Company Limited, Glasgow.
GreatBritain. Pp 365.
Hermanto, D Sadikin and E Hikmat. 2009. Deskripsi Varietas Unggul Palawija 1918-2009. Indonesian Center for
Food Crops Research and Development. Indonesian Agency for Agriculture Research and Development.
Pp 330 (In Indonesian).
Fehr WR. 1983. Applied Plant Breeding. Dept. of Agronomy, Iowa State Univ. Ames. 174 p.
Gomez KA and AA Gomez. 1984. Statistical Procedures for Agricultural Research. 2nd Edition. Pp 680.
Sugiyono 2009. Statistika untuk Penelitian. Alfabeta, Bandung. Pp 389 (In Indonesian).

th
Effect of Hydrogen Peroxide Spraying on Drought Stress
in Soybean Plant

Yushi Ishibashi
a
, Haruka yamaguchi
a
, Takashi Yuasa
a
, Mari Iwaya-Inoue
a
,
Susumu Arima
b,c
, Shao-Hui Zheng
c

a
Crop Science Lab., Faculty of Agricluture, Kyushu University, Hakozaki, Fukuoka 812-8581, Japan
b
Faculty of Agriculture, Saga University, Saga 840-8502, Japan
c
Coastal Bioenvironment Center, Saga University, Karatsu, Saga 840-0021, Japan
* Corresponding author: Yushi Ishibashi, Crop Science Lab., Faculty of Agriculture, Kyushu University,
Hakozaki, Fukuoka 812-8581, Japan. Tel.: +81 92 642 2824; fax: +81 92 642 2824.
[email protected]

Abstract

We examined whether the spraying of soybean leaves with hydrogen peroxide (H
2
O
2
) would alleviate the
symptoms of drought stress. Pre-treatment by spraying leaves with H
2
O
2
delayed foliar wilting caused by
drought stress compared to leaves sprayed with distilled water (DW). Additionally, the relative water content of
drought-stressed leaves pre-treated with H
2
O
2
was higher than that of leaves pre-treated with DW. Therefore,
we analyzed the effect of H
2
O
2
spraying on photosynthetic parameters and on the biosynthesis of
oligosaccharides related to water retention in leaves during drought stress. Under conditions of drought stress,
the net photosynthetic rate and stomatal conductance of leaves pre-treated with H
2
O
2
were higher than those of
leaves pre-treated with DW. In contrast to DW spraying, H
2
O
2
spraying immediately caused an increase in the
mRNA levels of D-myo-inositol 3-phosphate synthase 2 (GmMIPS2) and galactinol synthase (GolS), which
encode key enzymes for the biosynthesis of oligosaccharides known to help plants tolerate drought stress. In
addition, the levels of myo-inositol and galactinol were higher in H
2
O
2
-treated leaves than in DW-treated leaves.
These results indicated that H
2
O
2
spraying enabled the soybean plant to avoid drought stress through the
maintenance of leaf water content, and that this water retention was caused by the promotion of oligosaccharide
biosynthesis rather than by rapid stomatal closure.

Keywords: Drought stress, Galactinol, Hydrogen peroxide, Soybean

Introduction

Plants respond and adapt to water deficits at both the cellular and molecular levels by the
accumulation of osmolytes and proteins that are specifically involved in stress tolerance. Drought
stress is the primary cause of crop loss across the globe, reducing average yields in most major
crop plants (Boyer 1982; Bray et al. 2000).
It is known that drought stress enhances the production of reactive oxygen species (ROS)
in cellular compartments such as chloroplasts, peroxisomes, and mitochondria. If drought stress is
prolonged, ROS production will overwhelm the scavenging action of the antioxidant system,
resulting in extensive cellular damage and death (Cruz de Carvalho 2008). On the other hand, ROS
are also known to function as signal molecules in plants (Foyer et al. 1997), controlling

processes
such as growth, development, responses to biotic and

abiotic environmental stimuli, and
programmed cell death (Bailey-Serres and Mittler 2006).
Abscisic acid (ABA), synthesized in response to drought stress, is known to induce
stomatal closure and to reduce transpirational water loss (Schroeder et al. 2001). ABA activates the
synthesis of ROS in guard cells by a membrane-bound NADPH oxidase, and ROS mediate
stomatal closure by activating (through hyperpolarization) plasma membrane Ca
2+
channels (Pei et
al. 2000; Murata et al. 2001; Wang and Song 2008). In addition, it has been reported that hydrogen
peroxide (H
2
O
2
), a type of ROS, is involved in the acclimation of C. albidus to summer drought
(Jubany-Mar et al. 2009) and in that of maize (Zea mays L.) to salt stress (Azevedo Neto et al.
th
2005). H
2
O
2
also increases the soluble sugar content of melon fruits (Ozaki et al. 2009). Other
components may also be responsive to ROS as a part of a stress-activated signal transduction
pathway. We therefore focused on ROS as signal molecules by examining whether exogenous
H
2
O
2
application (by spraying) could alleviate drought stress and by working to define the alleviation
mechanism.


Plant materials
Soybean (Glycine max L. Merrill) cv. Fukuyutaka was used as the plant material. Three
weeks after emergence, either 1 mM H
2
O
2
or DW was sprayed only once onto the leaves of each
plant (100 mL/pot), and then irrigation was stopped. Treatments with H
2
O
2
or DW were always
followed by drought stress. Measurements of all parameters were made after water had been
withheld for 0, 2, 4, 6, and 8 days. For an additional control treatment, we included plants with no
spray treatment and with irrigation maintained throughout the experiment. The following
measurements consisted of four replicates.

Leaf relative water content
To evaluate leaf relative water content (RWC), 50 leaf discs (5 mm in diameter) from each
plant were weighed to determine fresh weight (FW), then hydrated to full turgidity by being floated in
DW for 24 h at 4 C and weighed again to determine the turgid fresh weight (TW). Dry weight (DW)
was determined by drying for 48 h at 90 C. RWC was then calculated as [(FW-DW)/(TW-
DW)]100.

Photosynthetic measurements
Photosynthetic rate, stomatal conductance, and transpiration rate were measured in
soybean leaves using an LCpro+ portable photosynthesis system (LCpro, ADC Bioscientific Ltd.,
UK) at room temperature (25 C) in the morning (8:00-11:00 am). The quantum flux density at the
leaf surface, flow rate, and leaf temperature in the chamber were maintained at 1500 mol m
-2
s
-1
,
200 mol s
-1
, and 30 C, respectively. The rate of CO
2
assimilation in the chamber was measured at
an ambient CO
2
concentration of 370 L L
-1
.

RT-PCR analysis
cDNA was synthesized from total RNA (1 g) using Rever TraACE reverse transcriptase
(Toyobo, Japan) according to the manufacturers protocol. cDNA (1 L)

was amplified in a reaction
containing 10 L of Go Taq Green Master Mix (Promega, USA), 0.1 L each

of 50 M forward and
reverse primers, and 8.8 L of water. The amplification was conducted using a Program Temp
Control System Astec PC-320 (Astec, Japan) as follows:

1 min at 94 C; 27 cycles of 15 s at 94 C,

30 s at 58 to 62 C, and 30 s at 72 C; then 5 min at 72 C. The specific primer sequences for
GmGolS (Glyma10g28610.1, Phytozome) were 5-GACAAGCTTAAGCAGCAGATGGGGCACGGA-
3 and 5-ATCGGATCCTGCCAGCAGCAGTGCCCCCATAAG-3; for GmP5CS (Genbank accession
no. AY492005), the specific primer sequences were 5-ATCAAGAGTTCCACTAAAATTCCTGTC-3
and 5-TCATATGAGAAGGTCTCTGTGAGTGTAG-3; for GmActin (Genbank accession no.
V00450), the specific primer sequences were 5-GCGTGATCTCACTGATGCCCTTAT-3 and 5-
AGCCTTCGCAATCCACATCTGTTG-3. The specific primer sequences for GmMIPSs were
determined according to Chappell et al. (2006).

th
0
20
40
60
80
0 2 4 6 8
R
e
l
a
t
i
v
e

w
a
t
e
r

c
o
n
t
e
n
t

Days after treatment

c
c
b
b
b
b
a
a
a
Myo-inositol and galactinol contents
Myo-inositol and galactinol levels were analyzed by HPLC using a 930-RI refractive index
detector (JASCO, Japan) and a Shodex Asahipak NH2P-50 4E column (polymer-base, particle size;
5 m, 250 mm 4.6 mm i.d.) (Showa Denko K.K., Japan). Sugars were separated with acetonitrile-
water (80:20, v/v) as an isocratic mobile phase at 0.8 mL/min using an 880PU pump (JASCO,
Japan). The column was held at 40 C.
Powdered freeze-dried leaves (50 mg) were extracted with 4 mL 80% (v/v) ethanol. The
extracts were boiled for 20 min and centrifuged for 5 min at 25 000g to produce pellets of insoluble
material. The supernatant was removed and the pellet was extracted twice more using the same
approach. The supernatants were then combined and dried. The residue was dissolved in 1 mL of
DW and passed through a Sep-Pak C18 mini-column (Waters, USA). The extracts were filtered
(0.45 m) before HPLC injection.


The RWCs for the three treatments are shown in Figure 1. There were no significant
differences in RWC between control, H
2
O
2
-treated, and DW-treated plants up to 2 DAT. At 4 DAT,
the RWCs in control, H
2
O
2
-treated, and DW-treated plants were 80%, 60%, and 40%, respectively.
The RWC at 6 DAT was also higher in H
2
O
2
-treated plants than in DW-treated plants. By 8 DAT, the
RWCs for both the H
2
O
2
and DW treatments were approximately 40%.

Figure 1. Relative water contents of soybean leaves during drought stress.

The net photosynthetic rate (P
N
), transpiration rate (E), and stomatal conductance (g
s
)
during drought stress are shown in Figure 2. Here, although the P
N
, E, and g
s
significantly
decreased during drought stress, these parameters were significantly higher in the H
2
O
2
-treated
plants than in DW-treated plants. At 2 DAT, g
s
levels in control, H
2
O
2
-treated, and DW-treated
plants were 0.588, 0.508, and 0.323 mol

m
-2
s
-1
, respectively (Fig. 2C). At 4 DAT, P
N
levels in
control, H
2
O
2
-treated, and DW-treated plants were 21.34, 9.36, and 5.51 mol

m
-2
s
-1
, respectively,
and the levels of E were 7.76, 3.35, and 2.53 mmol

m
-2
s
-1
, respectively (Fig. 2A, B).
Myo-inositol plays critical and diverse biological roles in a myriad of cellular processes
including signal transduction, stress responses, cell-wall biogenesis, growth regulation, and
osmotolerance (Loewus and Murthy 2000). At 2, 4, and 6 DAT, GmMIPS2 expression was markedly
higher in leaves treated with H
2
O
2
compared with control and DW-treated leaves (Fig. 3A). At 2
DAT, GmMIPS2 expression was induced by H
2
O
2
treatment but not by DW treatment. At 4 and 6
DAT, the expression of GmMIPS2 mRNA in H
2
O
2
-treated leaves was remarkably higher than that in
DW-treated leaves. In contrast, the expression of GmMIPS1, -3, and -4 did not vary among the
control, H
2
O
2
, and DW treatments. We also examined the expression of galactinol synthase (GolS),
Closed squares indicate the control (irrigated, unsprayed) treatment. Open and
closed circles indicate pre-treatment with H
2
O
2
and DW respectively, followed by
drought stress for the number of days indicated. For each day after treatment,
means followed by different letters are significantly different at the 5% level as
determined by Tukeys test (n = 4); error bars indicate standard deviations.
th
0
0.3
0.6
0.9
1.2
0 2 4 6 8
g
s
(
m
o
l

m
-
2
s
-
1
)
a
a
b
a
b
c
a
b
b
a
b
C
0
2
4
6
8
0 2 4 6 8
E

(
m
m
o
l
m
-
2

s
-
1
)
a
a
a
a
b
b
b
c
c
ab
b
B
0
5
10
15
20
25
0 2 4 6 8
P
N
(
m
o
l
m
-
2

s
-
1
)
a
a
a a
a
b
b
b
b
c
c
A
GmMIPS2
GmMIPS1
GmMIPS3
GmMIPS4
A
0
4
8
12
0 2 4 6 8
S
u
g
a
r

c
o
n
t
e
n
t
s

(
m
g
/
g

D
W
)
Myo-Inositol
a
b
c
a
b
c
a
b
c
0
0.5
1
1.5
2
2.5
0 2 4 6 8
Galactinol
a
b
a
a
b
c
a
b
c
a
b
c
B C
which acts downstream of MIPS in the synthesis of raffinose-family oligosaccharides (RFOs).
GmGolS expression was low in the control and DW-treated leaves but clearly higher in the H
2
O
2
treated leaves, especially at 4 and 6 DAT (Fig. 3A).

(A) Photosynthetic rate (P
N
); (B) transpiration rate (E); and (C) stomatal conductance (g
s
). Closed squares indicate control
(irrigated, unsprayed) treatment. Open and closed circles are H
2
O
2
and DW pre-treatments, respectively, followed by drought
stress for the number of days indicated. For each day after treatment, means followed by different letters are significantly
different at the 5% level as determined by Tukeys test (n = 4); error bars indicate standard deviations.

Figure 2. Photosynthetic parameters during drought stress.

Figure 3. Gene expression of GmMIPSs and GmGolS and contents of myo-inositol and galactinol in leaves
during drought stress.

We also found that the myo-inositol and galactinol contents in leaves pre-treated with H
2
O
2

were increased compared with control and DW-treated leaves (Fig. 3B, C). Myo-inositol contents
increased during drought stress, especially in H
2
O
2
-sprayed plants at 6 DAT, but decreased to
starting levels by 8 DAT (Fig. 3B). The galactinol content in leaves pre-treated with H
2
O
2
nearly
doubled by 4 DAT, and the increased level was maintained until 8 DAT. On the other hand, the
galactinol content in leaves pre-treated with DW increased until 8 DAT, but was significantly lower
from 4 to 8 DAT than that seen in H
2
O
2
-treated plants (Fig. 3C).
(A) Expression of GmMIPS genes and GmGolS.
Control (irrigated, unsprayed); H
2
O
2
, H
2
O
2
pre-treated;
DW, DW pre-treated; d, days after treatment. GmActin
was used as a control for loading. (B) Myo-inositol
contents and (C) galactinol contents. Closed squares
indicate the control (irrigated, unsprayed) treatment.
Open and closed circles indicate pre-treatment with
H
2
O
2
and DW, respectively, followed by drought stress
for the number of days indicated. Means followed by
different letters are significantly different at the 5%
level as determined by Tukeys test (n = 4); error bars
indicate standard deviations.
th
Stress-inducible production of galactinol synthase (GolS) plays a key role in the
accumulation of galactinol and raffinose, which function as osmoprotectants, under drought stress
(Taji et al. 2002). GolS catalyzes the synthesis of galactinol from myo-inositol

and UDP-galactose.
We therefore examined the transcript levels of D-myo-inositol 3-phosphate synthase1, -2, -3 and -4
(GmMIPSs), which encode key enzymes in the synthesis of myo-inositol, and that of GmGolS, in
H
2
O
2
-sprayed plants. We found that among the GmMIPS genes, only the transcript level of
GmMIPS2 increased after H
2
O
2
spraying (Fig. 3A). Chappell et al. (2006) reported that GmMIPS2
was poorly expressed in soybean leaves cultivated conventionally. The results reported here
suggest that GmMIPS2 is likely to be involved in drought stress signaling through ROS production
caused by drought stress. Treatment with methylviologen, which enhances the production of O
2
-
(another ROS), increased the transcript levels of GolS in Arabidopsis thaliana (Nishizawa et al.
2008). Overexpression of AtGolS2 in transgenic Arabidopsis thaliana caused an increase in
endogenous galactinol and raffinose, and showed improved drought tolerance (Taji et al. 2002). In
soybeans, we have shown that H
2
O
2
spraying increased the transcript level of GmGolS and the
galactinol content in leaves (Fig. 3A, C). These results suggest that H
2
O
2
spraying enabled the leaf
to maintain a high level of RWC by regulating the osmolality in the leaf, consequently alleviating the
effects of drought stress.

References

Azevedo Neto AD, Prisco JT, Eneas-Filho J, Medeiros JV, Gomes-Filho E. Hydrogen peroxide pre-treatment
induces salt-stress acclimation in maize plants. 2005. J. Plant Physiol. 162: 1114-22.
Bailey-Serres J, Mittler R. 2006. The roles of reactive oxygen species in plant cells. Plant Physiol. 141: 311.
Boyer JS. 1982. Plant productivity and environment. Science 218: 443-8.
Bray EA, Bailey-Serres J, Weretilnyk E. 2000. Responses to abiotic stresses. In: Gruissem W, Buchannan B,
Jones R, editors. Biochemistry and Molecular Biology of Plants. Rockville, MD. American Society of Plant
Physiologists Pp1158-1249.
Chappell AS, Scaboo AM, Wu X, Nguyen H, Pantalone VR, Bilyeu KD. 2006. Characterization of the MIPS gene
family in Glycine max. Plant Breed.125: 493-500.
Cruz de Carvalho MH. 2008. Drought stress and reactive oxygen species: production, scavenging and signaling.
Plant Signal Behav. 3: 156-65.
Foyer CH, Lelandais M, Kunert KJ. 1994. Photooxidative stress in plants. Physiol. Plant. 92: 696-17.
Jubany-Mar T, Munn-Bosch S, Lpez-Carbonell M, Alegre L. 2009. Hydrogen peroxide is involved in the
acclimation of the Mediterranean shrub, Cistus albidus L., to summer drought. J. Exp. Bot. 60: 107-20.
Murata Y, Pei Z-M, Mori IC, Schroeder JI. 2001. Abscisic acid activation of plasma membrane Ca2+ channels in
guard cells requires cytosolic NAD(P)H and is differentially disrupted upstream and downstream of reactive
oxygen species production in abi1-1 and abi2-1 protein phosphatase 2C mutants. Plant Cell 13:2513-23.
Nishizawa A, Yabuta Y, Shigeoka S. 2008. Galactinol and raffinose constitute a novel function to protect plants
from oxidative damage. Plant Physiol.147: 1251-63.
Ozaki K, Uchida A., Takabe T, Shinagawa F, Tanaka Y, Takabe T, Hayashi T, Hattori T, Rai AK, Takabe T.
2009. Enrichment of sugar content in melon fruits by hydrogen peroxide treatment. J Plant Physiol .166:
569-78.
Pei Z-M, Murata Y, Benning G, Thomine S, Klusener B, Allen GJ, Grill E, Schroeder JI. 2000. Calcium channels
activated by hydrogen peroxide mediate abscisic acid signalling in guard cells. Nature 406: 731-4.
Schroeder JI, Allen GJ, Hugouvieux V, Kwak JM, Waner D. 2001. Guard cell signal transduction. Annu. Rev.
Plant Physiol. Plant Mol. Biol. 52: 627-58.
Taji T, Ohsumi C, Iuchi S, Seki M, Kasuga M, Kobayashi M, Yamaguchi-Shinozaki K, Shinozaki K. 2002.
Important roles of drought- and cold-inducible genes for galactinol synthase in stress tolerance in
Arabidopsis thaliana. Plant J. 29: 417-26.
Wang P, Song C. 2008. Guard-cell signalling for hydrogen peroxide and abscisic acid. New Phytol.178: 703-18.

th
Productivity of Several Lines of Soybean in Majalengka,
West Java, Indonesia

Alia Astuti
a
, Ence Darmo Jaya Supena
a,b
, Suharsono
a,b,*

a
Department of Biology, Bogor Agricultural University, Indonesia
b
Research Center for Bioresources and Biotechnology, Bogor Agricultural University, Indonesia
*Corresponding author: PPSHB IPB, Gd PAU, Jl. Kamper, Kampus IPB Darmaga Bogor 16680, Indonesia
Tel: +62 251 8621257; fax: +62 251 8621724.
E-mail: [email protected]; [email protected]

Abstract

Soybean (Glycine max L. Merr) is a very important crop in Indonesia. The creation of new elite varieties is one
approach to increase the national production of soybean. We have developed several potential lines of soybean
to be released as a new varieties. Before releasing as new varieties, the productivity of these lines has to be
evaluated in several locations. Therefore the objective of this research was to evaluate the productivity of six
lines of soybean resulted from the cross between Slamet and Nokonsawon varieties, i.e. KH8, KH9, KH31,
KH38, KH55, and KH71 in Majalengka, West Java, Indonesia. Four national elite varieties i.e. Anjasmoro,
Slamet, Tanggamus and Wilis were used as standard. The experiment was conducted in two seasons by using
randomized block design, with three blocks as replication. The result showed that based on the seed production
per plant in two seasons, all six lines have higher productivity than Anjasmoro variety. The seeds of these six
lines are bigger than that of standard varieties. Analysis of production stability in two seasons showed that KH71
is the most stable genotype in Majalengka. By comparing to Anjasmoro variety in two seasons, all six lines have
a potential to be released as new varieties with high productivity and big seed.

Keywords: lines, productivity, seed size, soybean

Introduction

Soybean (Glycine max L. Merr) is a very important crop in Indonesia. Every year, Indonesia
imports more than 1.2 million tons of grains of soybean for food. The creation of new elite varieties
is one approach to increase the production of soybean in Indonesia. The creation of tolerant
varieties to acid soil containing high concentration of aluminum is very important to extend the
cultivation onto the marginal land with with this condition. Sunarto (1995) had created a variety of
Slamet which is tolerant to acid soil. Eventhough variety of Slamet has a high productivity and is a
tolerant to acid soil, it has a relatively small seeds and its hilum is black which are undesirable traits
for tofu and tempeh industry. To improve these traits, we had crossed this variety with
Nokhonsawon variety which has a big seeds, then followed by selection based on high productivity
and seed size traits (Suharsono et al., 2006, 2007; Jambormias et al., 2011). From this cross, we
obtained 18 potential lines to be released as a new variety.
Before releasing a line of soybean as new variety, the productivity of this line has to be
evaluated in several locations. In this experiment, six of 18 potential lines of soybean were
cultivated in the irrigated rice field in Majalengka, West Java, Indonesia. Majalengka is a center of
soybean production in West Java. So, the objective of this research was to evaluate the productivity
and seed size of six lines, i. e. KH 8, KH 9, KH 31, KH 38, KH 55, and KH 71, with four elite national
varieties, i. e. Anjasmoro, Slamet, Tanggamus, and Wilis as standard in two seasons in Majalengka,
West Java, Indonesia.

th

Six lines of soybean i.e. KH8, KH9, KH31, KH38, KH55, and KH71 were used in this
experiment. Four national cultivars i.e. Slamet, Wilis, Anjasmoro and Tanggamus were used as
standard. The experiment was carried out in Randomized Block Desain with three replications, so
this experiment had 30 experimental units or plots. The size of plot is 4 m x 5 m, planting distance is
40 cm x 20 cm with two plants per hole, so the productivity per hectar is productivity per plant x
250,000. The plants were fertilized by 10 tons of manure, 100 kg urea, 150 kg SP3, and 100 kg KCl
per ha in the beginning of cultivation. The evaluation of plant productivity was carried out by
sampling. For sampling, 10 plants were ramdomly chosen per plot. Seed size was mesured by
weighing 100 dry seeds which were ramdomly chosen.
The cultivation was carried out in two seasons, i. e. wet and dry seasons. The cultivation in
wet season (season I) was caried out in December 2009 - March 2010, and in dry season was done
in May - August 2010. The data of seed productivity per plant and seed size were analyzed by
Duncan Multiple Range Test. The clustering of genotype based on seed productivity per plant and
seed size was carried out by Important Performance Analysis (IPA). The analysis of stability of seed
productivity in two season was carried out by Additive Main Effect Multiplicative Interaction (AMMI).


Seed productivity and seed size
The seed productivity of all genotype (KH lines and standard varieties) in the wet season
was very high, between 22.9 and 35.6 g per plant, equivalent to 5.7-8.9 tons per ha. This
productivity is higher than that in dry season that is between 15.35 and 20.45 g per plant equivalent
to 3.8- 5.1 tons per ha (Table 1). Based on the description of Ministry of Agriculture (Deptan, 2011),
the productivity of Anjasmoro, Slamet, Tanggamus, and Wilis is 2.25-2.3, 2.26, 1.22, and 1.6 tons
per ha respectively. This productivity is lower than that of the same variety in Majalengka that is
more than 5 tons per ha (Table1). This result indicates that the environment of cultivation in
Majalengka was very favorable for soybean. The soil of this experiment has a pH 5.9 and contains
65,3 ppm of P which are very favorable for soybean growth.

Table 1. The productivity of several genotype in wet and dry seasons

Genotype
Productivity in wet season Productivity in dry season
Average of
Productivity
g/plant* kg/ha g/plant* kg/ha g/plant kg/ha
KH8 24.74 ab 6,185 17.7 ab 4,425 21.22 5,305
KH9 30.58 bc 7,645 20.45 c 5,113 25.52 6,380
KH31 22.89 a 5,723 19.02 bc 4,755 20.96 5,240
KH38 29.36 b 7,340 19.43 bc 4,858 24.4 6,100
KH55 35.62 c 8,905 17.71 ab 4,428 26.67 6,668
KH71 30.27 bc 7,568 17.06 ab 4,265 23.67 5,918
Anjasmoro 23.43 a 5,858 17.30 ab 4,325 20.37 5,093
Wilis 29.64 b 7,410 16.19 a 4,048 22.92 5,730
Tanggamus 30.56 bc 7,640 15.35 a 3,838 22.96 5,740
Slamet 24.74 ab 6,185 15.42 a 3,855 20.08 5,020
*the number followed by the different letter in the same column is significantly different.

Comparing to Anjasmoro which is elite national variety, all lines have equal or higher
productivity in wet and dry seasons. This result indicates that all lines have a potential as elite
th
national variety with a potential yield more than 5 tons per ha. In wet season, KH55 line has a
highest productivity, and in dry season KH9 has a highest productivity.
If we compare between wet and dry seasons, all genotypes have a higher yield in wet
season than in dry one. In this experiment, the precipitation during wet season in Majalengka was
about 411,53 mm/month, and during dry season was about 202 mm/month. Based on Calvino &
Sadras (1999), the precipitation more than 300 mm/month is better for production of soybean.
In average, all lines and Anjasmoro variety have a big seed, and bigger than the seeds of
Wilis, Tanggamus and Slamet varieties (Table 2). The big size is very important in the production of
tofu because the rendement is depend on the endosperm, and the endosperm of bigger seeds is
bigger than small ones. So, based on the size of seeds, all lines have a potential to be released as
a big seed varieties. As the yield, the size of seeds was also bigger in the wet season than that in
dry ones. The size of seeds may be affected by the enironment of growth. KH31 and KH38 have
bigger seeds compared to other genotypes.

Table 2. The size of seed of several genotype in two seasons

Genotype
Size of seed (g/100)
Wet season Dry season Average
KH8 21.76 e 16.80 bcd 19.28
KH9 22.88 e 15.50 b 19.19
KH31 21.71 e 19.50 e 20.61
KH38 22.82 e 18.46 cde 20.64
KH55 19.00 bc 16.03 b 17.52
KH71 20.74 de 18.70 de 19.72
Anjasmoro 18.50 c 16.60 bc 17.55
Wilis 14.42 ab 10.83 a 12.63
Tanggamus 12.60 a 10.76 a 11.68
Slamet 15.42 b 12.30 a 13.86

Clustering of genotype
In wet season, except KH31 line, other lines have higher seed productivity and seed size
compared to Anjasmoro variety. In dry season, KH8, Kh31 and KH38 lines have higher productivity
and seed size compared to Anjasmoro variety (Figure 1). This result indicated that KH8 and KH38
lines are consistently better than Anjasmoro variety.

Figure 1. Clustering genotype of soybean based on seed productivity and seed size in wet and dry seasons.
Seed size (g/100 seeds)
S
e
e
d

p
r
o
d
u
c
t
i
v
i
t
y

p
e
r

p
l
a
n
t

(
g
)

Wet season (M1)
S
e
e
d

p
r
o
d
u
c
t
i
v
i
t
y

p
e
r

p
l
a
n
t

(
g
)

Seed size (g/100 seeds)
Dry season (M2)
th
Analysis of stability of seed productivity in two seasons showed that KH71 is the most stable
genotype in Majalengka. KH9, KH38 and KH55 lines were more stable than Anjasmoro variety in
wet and dry seasons than Anjasmoro Variety (Figure 2). If we consider to the seed productivity, the
size of seeds and the stability of seed productivity, KH38 and KH71 are a potential lines to be
developed to become elite national varieties.

32 30 28 26 24 22 20 18 16
3
2
1
0
-1
-2
-3
rata-rata
K
U
1
M2
M1
WILIS
TANGGAMU
SLAMET
KH9
KH8
KH71
KH55
KH38
KH31
ANJASMOR
BIPLOT AMMI I

Figure 2. Stability of seed productivity in wet and dry season of soybean in Majalengka. M1= wet season, M2=
dry season.

Acknowledgement

This research was financially supported by I-MHERE B2c IPB entitled: Test of adaptability of several
elite lines of soybean in several locations in the frame of the creation of new elite cultivars, contract No:
13/13.24.4/SPP/I-MHERE/2010 on behalf of Suharsono.

References

Calvino PA, Sadras VO. 1999. Interannual variation in soybean yield: interaction among rainfall, soil depth and
crop management. Field Crops Research 63: 237-246.
[Deptan] Departemen Pertanian. 2011. Daftar varietas unggul kedelai, http://pangan.litbang.deptan.go.id/index.
php?bawaan=varietas/gerbang&proses=daftarstok&komoditas=05025&varietas=1 [05 Juli 2011].
Jambormias E, Sutjahjo SH, Jusuf M, Suharsono. 2011. Using information from relatives and path analysis to
select for yield and seed size in soybean (Glycine max L. Merrill). Sabrao J. Breeding Genet 43 (1): 44-
58
Suharsono, Jusuf M, Paserang AP. 2006. Analisis ragam, heritabilitas, dan pendugaan kemajuan seleksi
populasi F2 dari persilangan kedelai kultivar Slamet x Nokonsawon. J Tanaman Tropika 9:86-94.
Suharsono, Jusuf M, Dasumiati. 2007. Analisis ragam, dan seleksi populasi F3 dari persilangan kedelai kultivar
Slamet x Nokonsawon. J Tanaman Tropika 10: 21-28.
Sunarto. 1995. Pemuliaan kedelai untuk toleransi terhadap tanah masam dan keracunan Aluminium. Jurnal
Tanaman Industri dan Pangan 12(2): 98-99.

P
r
i
n
c
i
p
l
e

c
o
m
p
o
n
e
n
t

o
f

S
e
e
d

p
r
o
d
u
c
t
i
v
i
t
y

Average of seed productivity (g)
th

th
Paclobutrazol Application Effectiveness on Growth of Two Peanut
(Arachis hypogaea L.) Varieties

Iskandar Lubis
a,*
, Aries Kusumawati
b
, Munif Ghulamahdi
c
, Heni Purnamawati
a
, Yudiwanti
WE Kusumo
d
, Ahmad Ghozi Mansyuri
e
, Sri Astuti Rais
f

a
Laboratory of Crop Production, Department of Agronomy and Horticulture, Faculty of Agriculture,
b
Depatment of Agronomy, Faculty of Agriculture, Andalas University
c
Laboratory of Ecophysiology, Department of Agronomy and Horticulture, Faculty of Agriculture,
d
Laboratory of Plant Breeding, Department of Agronomy and Horticulture, Faculty of Agriculture,
e
Legume and Tuber Crop Research Center, Indonesian Ministry of Agriculture
f
Gen Resource and Biotechnology Research and Development Center, Indonesian Ministry of Agriculture
*Corresponding author: Lab of Crop Production, Department of Agronomy and Horticulture,
Faculty of Agriculture, Bogor Agricultural University.
Jalan Meranti 1, Kampus IPB Dramaga, Bogor 16680. Indonesia
Tel/Fax: +62-251-8629353.
[email protected]

Abstract

Peanuts productivities in Indonesia during 19862003 ranged 0.7 to 1.2 ton/ha dry seeds, although some new
varieties having potential yield from 2.0 to 2.5 ton/ha or more, farmers productivity reached only 5060% of the
yield. This research was conducted to investigate the effectiveness of paclobutrazol on the growth and
production of peanuts. Experiment was conducted at Bogor Agricultural University farms at Cikabayan. Planting
was conducted in April to July 2009, using 2 peanut Varieties, namely Sima and Kelinci. Design of experiment
was Split-split plot. Paclobutrazol was applied at 6 and 8 Weeks after Planting, WAP as main plot, Varieties
(Sima and Kelinci) was used as sub plot and concentrations of Paclobutrazol (0, 100 and 200 ppm) was used as
sub-sub plot with three replicates. Size of experimental unit was (3 x 5) m
2
, with planting density of 125 000
plants/ha. Urea, SP36 and KCl were applied at planting date at 33.75 kg N, 36 kg P
2
O
5
and 45 kg K
2
O per ha,
respectively. Observation covered growth and production, such as dry matter production, leaf area index, pod
number, pod weight, non-structural carbohydrate and total nitrogen in the stem. The results showed that
paclobutrazol concentration at 200 ppm increased pod weight and productivity of peanuts, however, did not
affect the total soluble carbohydrate and nitrogen content in the stem at 10 WAP. Sima had vigorous growth
than that of Kelinci variety showing bigger leaf area and higher chlorophyll.

Keywords : Peanut, paclobutrazol, growth

Introduction

Peanuts productivities in Indonesia during 19862003 ranged from 0.7 to 1.2 ton/ha of dry
seeds (Kasno, 2004), although some new varieties having potential yield from 2.0 to 2.5 ton/ha or
more have been released, farmers productivity reached only 5060% of the potential yield.
Productivity is related with empty and or imperfect pod filling. Bell and Right (1998) found that
peanut population in Indonesia is relatively high, however, many of pod produced empty or partly
filled. Lukitas (2005) and Khasanah and Purnamawati (2007) reported that only 26-68% (in average
46%) of gynophores became filled pod. Physiological modification of plant growth by controlling the
vegetative growth is one of method overcomes the problem. Growth regulator is used in order to
maintain vegetative and reproductive growth balance. It can be suppressed the competition
vegetative and generative growth which may decrease assimilate distributed to the sink (Cruz-
Aguado et al., 1999; Arzani and Roosta, 2004).
th
Peanut is a semi determinate crop has vegetative growth continuously even if reach the
flowering stage. In order to maximize assimilate for filling the pod, it is necessary to investigate
source size modification and sink-source balance in peanut. Therefore, retardant as a growth
regulator can be used for regulating plant growth balance. Banon et al. (2002) reported that one of
growth retardant widely used is paclobutrazol. Moreover, Seeno and Isoda (2003) reported that
foliar application of paclobutrazol at 100 and 200 ppm in the stage of initial pod formation and initial
and medium pod filling increased seed production of peanuts.
This research aims were to investigate the effect of time application of paclobutrazol on the
growth of peanuts; to optimize the paclobutrazol concentration to growth and production of peanuts;
and to investigate the growth pattern and production of peanuts.


Experiment was conducted at Bogor Agricultural University farm at Cikabayan. Planting
was conducted for four months from April to July, 2009. Analysis was done at laboratory of RGCI
(Research Group of Crop Improvement), Department of Agronomy and Horticulture, Faculty of
Agriculture, Bogor Agricultural University. Materials for experiment were peanut seed of Kelinci and
Sima varieties, Urea, SP36 and KCl as fertilizers, KCl was applied at planting date at 33.75 kg; N at
36 kg; P
2
O
5
of 45 kg K
2
O per ha, respectively. Paclobutrazol was used as retardant.
Design of experiment was Split-split plot design where Time of Paclobutrazol applications
(at 6 and 8 Weeks after Planting, WAP) was used as main plot, Varieties (Sima dan Kelinci) was
used as sub plot and Dosage of Paclobutrazols (0; 100 and 200 ppm) was as sub-sub plot with
three replicates, Size of experimental unit was (3 x 5) m
2
, with planting density of 125 000 plants/ha.
Data were analyzed by F test at 5% level, and advanced test used Duncan Multiple Range Test
(DMRT) in 5% level.
Observation included physiological character, growth and production. Growth component
covered total dry matter, stem and leaf weight and leaf area index (LAI). Production component
covered total number of pod, pod weight and productivity, while physiological character covered
chlorophyll, total non-structural carbohydrate (TNC) and stem nitrogen content.


The results showed that the single treatment affected the growth of peanut. There was no
interaction among time of application, concentration of paclobutrazol and variety. Time of
application had significant effect on 8 WAP of peanut. Effect of variety was significant for plant
height, total dry matter, culm and leaf dry weight, number of gynophores and pod, 100 seed weight
and harvesting index, respectively. Paclobutrazol application had significant effect on plant height,
stem dry weight, leaf number, pod number per plant, pod weight per plant, seed weight per plant,
seed number per plant and plant productivity, respectively.

Leaf Area Index (LAI)
Statistical analysis showed that at 8, 10 and 12 WAP, LAI was significantly affected by
variety. At 12 WAP, Sima had LAI of 4.48 which was significantly higher than that of Kelinci (3.55)
(Figure 1). Slow initial growth in peanuts was performed by slow LAI development. Then LAI
reached value of 5.5 and 7.0, respectively. Although LAI was higher, assimilate supply still restricted
seed yield, this could be to its used for maintaining higher LAI and compensating dead leaf. Then
growth of leaf may compete with the development of the sink organ (Gardner et al., 1991).

th

Figure 1. Leaf Area Index of Peanut varieties. Number followed by similar letter is not significant in 5% level.

Pod Number per Plant
Statistical analysis showed that time application of paclobutrazol and varieties had no
significant effect on pod number per plant. There was only the concentration of paclobutrazol having
significant effect on the pod number per plant. The highest number of pod represented by 200 ppm
paclobutrazol reaching 14 pods per plant, while 0 and 100 ppm produced similar number (12) of
pods per plant, respectively, as shown in Figure 2.

Figure 2. Total number of pod per plant after paclobutrazol treatment.

Productivity
Peanut productivity in this experiment represented by pod dry weight per ha. Statistical
analysis showed that paclobutrazol concentration significantly affected peanut productivity. The
highest productivity performed by 200 ppm paclobutrazol concentration which was 1.18 ton per ha,
while concentration 0 and 100 ppm had no significant differences in productivity (Figure 3).

Figure. 3 Productivity after paclobutrazol treatment.
th
Chlorophyll content
Time of application and paclobutrazol concentrations did not have significant effect on the
chlorophyll content. While variety significantly affected the chlorophyll content, and Sima has higher
chlorophyll content than Kelinci (Figure 4). Yudiwanti (2007) stated that peanut which has dark
green color has higher chlorophyll content and has high yield potential and tolerant to bacterial leaf
blight. It is also supported by Taiz and Zeiger (2002) stated that highest content of chlorophyll
visually performed by greenness of leaf, and dark green leaf will more efficient to catch solar
radiation for photosynthesis.

Figure 4. Chlorophyl content of peanut varietyof Sima and Kelinci.

Total Soluble Carbohydrate and Nitrogen Contents
There was no significant effect of paclobutrazol concentration on the content of total
soluble carbohydrate (TNC) and Nitrogen content in the stem at 10 WAP, however, the content of
TNC in 200ppm was absolutely higher than that of 0 or 100 ppm of paclobutrazol, and in the
opposite nitrogen content in 200 ppm was absolutely lower than that at 0 and 100 ppm
paclobutrazol, respectively (Figures 5a and 5b).
The effort for increasing potential yield of peanuts is important role in order to
breakthrough barrier from physiological factors. The first step is to assess growth of yield organ, is it
limited by availability of source or by sink capacity. Recently, genotype differences in allocation and
mobilization pattern of assimilate in the stem of wheat has been sown (Cruz-Aguado et.al. 1999).

( a )

( b )

Figure 5. Soluble carbohydrate (a) and Nitrogen (b).content in the stem at 10 WAP as affected by paclobutrazol
concentration.

th
Conclusion

Paclobutrazol concentration at 200 ppm increased pod weight and productivity of peanuts,
however, it had no significant effect on total soluble carbohydrate and nitrogen content in the stem
at 10 WAP. Sima had vigorous growth than that of Kelinci variety showed by bigger leaf area and
higher chlorophyll content in the leaf.

References

Arzani, K., H.R. Roosta. 2004. Effect of Paclobutrazol on Vegetatif and Reproductive Growth and Leaf Mineral
Content of Mature Apricot (Prunus armeiaca L.) Trees. J.Agri.Sci.Technol. 6:43-55.
Banon, S., A. Gonzales, E.A. Cano, J.A. Franco, J.A Fernandes. 2002. Growth, Developmentand and Colour
Response of Potted (Dianthus caryophyllus cv. Mondriaan to Paclobutrazol Treatment. Scientia
Horticulturae 94: 371 377.
Bell, M.J., G.C. Wright. 1998. Groundnut Growth and development in Contrasting Environment. 1. Growth and
Plant Density Responses. Ekperimental Agriculture 34 : 99 112.
Cruz-Aguado, J.A., F. Reyes, R. Rodes, I. Perez, M. Dorado. 1999. Effect of Source-to-Sink Ratio on
Partitioning of Dry Matter and
14
C-photoassimilates in Wheat during Grain Filling. Annals of Botany 83:
655 665.
Gardner, F.P., R.B. Pearce, R.L. Mitchell. 1991. Fisiologi Tanaman Budidaya. UI Press. Jakarta. 428 hal.
Khasanah, U., H. Purnamawati. 2007. Pertumbuhan dan Produktifitas 5 Varietas Kacang Tanah. [Makalah
Seminar Skripsi]. Departemen Agronomi dan Hortikultura Fakultas Pertanian, Institut Pertanian Bogor. 7
hal.
Kasno, A. 2005. Profil dan Perkembangan Teknik Produksi Kacang Tanah di Indonesia. Seminar Rutin
Puslitbang Tanaman Pangan. Bogor. 15 hal.
Lukitas, W. 2005. Uji Daya Hasil Lima Kultivar Kacang Tanah. Skripsi. Departemen Budidaya Pertanian
Fakultas Pertanian IPB. 39 hal.
Seeno, S., A. Isoda. 2003. Effect Paclobutrazol on Dry Matter Distirbution and Yield Peanut. Plant Production
Science Vol. 6. P90-94.
Taiz, Zeiger. 2002. Plant Physiology (3
rd
edition). Sinauer Associates, Inc. Massachutes, USA.
Yudiwanti. 2007. Galur Kacang Tanah Berdaun Hijau Tua: Keunggulan dan Pengendalian Genetiknya.
Prosiding Seminar Nasional Hasil Penelitian yang dibiayai oleh Hibah Kompetitif; Bogor, 1 2 Agustus
2007. Hlm 143 146.

th
Effect of Source or Sink Restriction on Flowering, Podding, and Yield
Performance in Field-Grown Adzuki Bean

Shinya Kasajima
a,*
, Hirotake Itoh
a
, Yasuo Nakamaru
a
, Hozumi Yoshida
a
, Hitoshi Sato
b

a
Faculty of Bioindustry, Tokyo University of Agriculture, Hokkaido, Japan
b
Hokkaido Research Organization Tokachi Agricultural Experiment Station, Hokkaido, Japan
* Corresponding author: Faculty of Bioindustry, Tokyo University of Agriculture, Yasaka 196, Abashiri,
Hokkaido 099-2493, Japan.
Tel.: +81 152 48 3823
[email protected]

Abstract

The effect of source or sink restriction on flowering, podding, and yield performance in field-grown adzuki bean
cv. Erimo-shozu was investigated. Defoliation and defloration treatments were performed as source and sink
restriction during the flowering period. Defoliation treatment reduced the flower and pod numbers and shortened
the period of flowering and podding. Defloration increased the flower and pod numbers. Defoliation treatment
was shown to reduce the seed yield and yield components. The 100-grain weight in defoliation treatment was
significantly the lowest among all treatments. These results suggest that the seed yield of adzuki bean depends
on dry matter production during the flowering period. Furthermore, a compensatory effect in sink restriction
indicated by an increase in flower number was also noted.

Keywords: adzuki bean, defloration, defoliation, flowering, podding, yield component

Introduction

Adzuki bean (Vigna angularis (Willd.) Ohwi et Ohashi) is the second most important
leguminous crop in Japan after soybean (Glycine max (L.) Merr.). It is widely used for the
production of a sweet bean paste called Ann, which is a major component in traditional Japanese
sweets (Murata, 1999). It has been commercially produced in Hokkaido, Northern Japan, where
crop breeding program is mainly carried out in that area (Shimada, 2006). In recent years,
improvement of yield stability is an important issue to be considered since the production efficiency
of adzuki bean grown in Hokkaido varies drastically each year because of higher rates of damage
due to cold weather (Shimada, 2006). However, up-to-date information with regard to the yield-
determining process of adzuki bean has been limited because of its minor role worldwide.
In adzuki bean, as in many other leguminous crops, knowing the habit of flowering and
podding is considered to be important for analyzing the yield-determining process. Compared to the
soybean, the adzuki bean has a long flowering period and a low podding efficiency (Takahashi,
1958). In general, source-sink relationships play an important role in the yield-determining process.
For example, defoliation or defloration treatments of soybean plants accelerated the development of
flower buds and podding (Saitoh et al., 2001). However, there is limited information about the effect
of source or sink restriction on flowering, podding, and yield performance of adzuki bean. In order to
evaluate the relative importance of source or sink on yield-determining process, we examined the
changes in flower and pod numbers and yield components in field-grown adzuki bean plants as
affected by defoliation or defloration treatments.

th

The field experiment was conducted in the Tokyo University of Agriculture farm at Abashiri,
Hokkaido, Japan (435344N, 1442145E). The soil type was andosol, and the preceding crop
was barley (Hordeum vulgare L.). Adzuki bean cv. Erimo-shozu, which is a most famous leading
variety of adzuki bean in Hokkaido, was used in this study. Four seeds per hill were seeded on June
2, 2010, at 16.6-cm spacing in approximately 3.5-m-long rows with 72-cm row spacing. The
seedlings were thinned to two seedlings per hill three weeks after seeding. Compound fertilizer
(N:P
2
O
5
:K
2
O = 5:25:14%) at 80 g m
2
was applied as the basal application. Although the summer
air temperature in 2010 was higher than that in the average year, this experiment was performed
under normal climatic conditions.
Source or sink restriction treatment was initiated on July 26, after flowering began. Source
restriction treatment consisted of removing two lateral leaflets of every trifoliate leaf when flowering
began. Sink restriction treatment consisted of removing every flower on each branch. After initiation,
defoliation and defloration were continued until flowering ceased. Six experimental plots including a
control were set up according to a randomized block design with two replications.
The change in flower and pod numbers was investigated for 5 plant samples in each plot.
The flowering date was recorded on a small label (9 mm in width and 22 mm in length) for each
plant, and then the label was wrapped around the pedicel of the flower. The labels were attached on
all flowers that had formed pods by the time of maturity. The podding rate was calculated from the
flower and pod numbers during the entire flowering period based on the label data. At maturity, 20
standard plants from 10 hills in each plot were sampled except for the plant with attached labels.
After air-drying, the seed yield and yield componentsnamely, pod number, seed number per pod,
and 100-seed weightwere examined.


The average temperatures during the vegetative and reproductive stages were 17.5C and
19.6C, respectively. The growth and yield of adzuki bean are known to be susceptible to cold
weather damage (Shimada, 2006), e.g., the low temperature during vegetative growth induced
abortion of main stem elongation, and low temperature before flowering induced podding injury in a
previous study (Aoyama et al., 2009). In the present experiment, air temperature during every
growth phase tended to be higher than that in the average year. The main stem length and top dry
weight at maturity in control treatment condition were 83.4 cm and 640 g m
2
, respectively. It was
confirmed that in the normal plant type, flowering and podding were not affected by low
temperatures.
The change in flower and pod numbers per plant differed among treatments (Fig. 1). In
control treatment, the cumulative flower and pod numbers per plant were 104.0 and 56.4,
respectively (Fig. 1A). In source restriction treatment, however, the flower and pod numbers were
reduced and the period of flowering and podding was shortened compared to control (Fig. 1B). Data
indicated that dry matter production after flowering affects the flower and pod numbers.
Furthermore, this study clarified that the reduction in dry matter production also affects the flowering
and podding periods. Conversely, the flower and pod numbers in sink restriction treatment were
higher than those in the control but the podding rate was lowest among all treatments (Fig. 1C).
These results suggested that sink restriction treatment was compensated by a drastic increase in
the flower number. In this study, sink restriction treatment consisted of removing all flowers from all
branches. The effects of source and sink manipulations on the flower numbers of soybean varied
with flower position between the main stem and branches (Saitoh et al., 2001). Thus, further studies
are required to clarify the source-sink relationship between the main stem and branches of adzuki
bean.
th
Table 1 showed the effect of source or sink restriction on the seed yield and yield
components of adzuki bean. The seed yield tended to be lower in source restriction treatment than
in control and sink restriction treatments, although no significant difference was observed. Similar
tendencies were observed in yield components. The 100-seed weight in source restriction treatment
was significantly lower than the weights in other treatments. The decline in 100-seed weight by
defoliation suggested that the seed yield of adzuki bean might be limited by source size, which was
consistent with previous reports on soybeans (Egli & Leggett, 1976; Saitoh et al., 2001).

Table 1. Effect of source or sink restriction on the seed yield and yield components of adzuki bean

Treatment Seed Yield (g m
-2
) Pod no. (no. m
-2
) Seed no. per Pod
100-seed weight
(g)
Control 358 a 487 a 5.52 a 12.9 a
Source restriction 305 a 438 a 5.42 a 12.1 b
Sink restriction 338 a 463 a 5.48 a 13.0 a
Values with different letters in a single column are significantly different at the 5% significance level by TukeyKramers test.

0
1
2
3
4
5
7/25 7/30 8/4 8/9 8/14 8/19 8/24 8/29
Flower no. per plant : 104.0
Pod no. per plant : 56.4
Podding rate (%) : 54.2
0
1
2
3
4
5
7/25 7/30 8/4 8/9 8/14 8/19 8/24 8/29
0
1
2
3
4
5
2
5
-
J
u
l
3
0
-
J
u
l
4
-
A
u
g
9
-
A
u
g
1
4
-
A
u
g
1
9
-
A
u
g
2
4
-
A
u
g
2
9
-
A
u
g
N
u
m
b
e
r

o
f

f
l
o
w
e
r
s

a
n
d

p
o
d
s

p
e
r

p
l
a
n
t
(A)
(B)
(C)
Flower number Pod number

Data shows 5-days moving average with 10 plants of 2 replicates. The flower number, pod number, and podding rate in each
figure show the values of entire examination periods.

Figure 1. The change in flower and pod numbers per plant in control (A), source restriction (B), and sink
restriction (C).
th
In conclusion, this study suggested that the seed yield of adzuki bean depends on dry
matter production during the flowering period. A compensatory effect in sink restriction treatment
indicated by an increase in flower number was also observed. Moreover, defoliation treatment
shortened the flowering and podding periods. This result may be related to early maturity. In the
future, we plan to conduct additional experiments using early maturing varieties.

References

Aoyama S, H Shimada, N Hasegawa, K Murata, S Fujita and I Matsukawa. 2009. A new early maturing adzuki
bean variety Kita-roman with cool-weather tolerance and soil-borne disease resistance. Bulletin of
Hokkaido Prefectural Agricultural Experiment Station 94: 1-16**.
Egli DB and JE Leggett. 1976. Rate of dry matter accumulation in soybean seeds with varying source-sink
relations. Agronomy J. 68: 371-374.
Murata K. 1999. Breeding of adzuki bean cultivar Erimo-shozu and cultivars with large seeds or resistance to
soil-borne diseases in Hokkaido. Breed. Res. 1: 173-179*.
Saitoh K, S Isobe, Y Seguchi and T Kuroda. 2001. Effects of source and/or sink restriction on the number of
flowers, yield and dry-matter production in field-grown soybean. Jpn. J. Crop Sci. 70: 365-372**.
Shimada H. 2006. Circumstances of adzuki bean production in Hokkaido and future direction of breeding adzuki
bean. J. Agr. Sci. 61: 11-15*.
Takahashi N. 1958. Ecological studies of fruiting behaviours of adzuki beans (Phaseolus angularis W. F. Wight).
Proc. Crop Sci. Soc. Jpn. 26: 43-44***.

*In Japanese.
** In Japanese with English summary.
*** In English with English abstract.

th
th
Analysis of Genes Expressed during the Early Maturation of Sesame Seeds

Motonobu Yoshida, Akihiro Kishikawa, Takayuki Nakano, Eiji Tanesaka

Lab of Plant Breeding and Agrobiotechnology, Department of Agricultural Science
Kinki University
Nakamachi 3327-204, Nara 631-8505, Japan
Tel: 81-742 43 5245, Fax: 81-742 43 1155
[email protected]

Abstract

Sesame seeds of cultivated species, Sesamum indicum, contain abundant oil, in particular, large amounts of
unsaturated fatty acid oleic and linoleic acids. Total amounts of oleic and linoleic acids in sesame seeds keep
constant among varieties of S. indicum. However, the regulation of the mechanism is unknown. Therefore, this
study attempted to clarify these points through transformation of Arabidopsis thaliana with novel genes in
sesame seeds. Oil contents increase rapidly in sesame seeds within 4 weeks after flowering. A full-length cDNA
library prepared from sesame seed of 1 to 3 weeks oldwas substracted with cDNAs from plantlets of 4 weeks
after germination. The results showed that the cDNA library was expressed specifically during the early
maturation.The 1,545 cDNA clones were sequenced. Of these, 30.3% of the clones were responsible for protein
destination, 16.7% of the clones for the metabolism, and 6.9% of the clones for the cell growth and division.
Among them, 13 genes for a transcription factor were identified, four were identified as a transcription factor
involved in ethylene signaling. In addition, nine genes: osmotin-like protein, expansin-like protein, aquaporin-like
protein, MADS-box protein 4, novel putative uncharacterized protein, ethylene response factor 2, ethylene
responsive element binding protein 3, AP2 containing transcription factor and lipid transfer protein were
analyzed by overexpression of A. thaliana. The A. thaliana overexpression strain for novel putative
uncharacterized protein and aquaporin-like protein, respectively showed the increase of unsaturated fatty acids.
The amount of oleic acid per seed grain in a strain for novel protein was 1.7 fold, and that of linoleic acid 1.5
fold, respectively.

Keywords: Sesamum indicum, fatty acids, full-length cDNA, Arabidopsis transformation

Introduction

Sesame seeds of cultivated species, Sesamum indicum, contain abundant oil, in particular,
large amounts of unsaturated fatty acid oleic and linoleic acids. These unsaturated fatty acids lower
the cholesterol level in the body (Satchithanandam et al., 1993). Because of their effects and
antioxidant substances, attention has been paid to sesame seeds as health food (Budowski and
Markley, 1951). Total amounts of oleic and linoleic acids in sesame seeds are constant among
varieties of S. indicum. However, the regulation of the mechanism is unknown. It is necessary to
clarify these points to breed novel varieties with high content of unsaturated fatty acids. Oil contents
of sesame seeds increase rapidly within 4 weeks day after flowering (DAF). Therefore, this study
attempted to analyze the function of novel genes expressed specifically during the early maturation
of sesame seeds through transformation of Arabidopsis thaliana with novel genes of sesame seeds.


Plant materials and growth conditions
Sesamum indicum seeds were obtained from Toyama University. Arabidopsis thaliana
plants were grown under continuous light at 22-23
o
C and used for transformation.

th
Preparation of a full-lengh cDNA library and cDNA materials
Total RNAs were prepared from S. indicum seeds of 1 to 3 weeks old. A full-length cDNA
library was prepared using pCMVFL3 vector as described previously (Uenishi et al., 2004). Total
RNAs from young plants were extracted four weeks after germination. After purification of poly
(A)
+
RNA, cDNA materials were synthesized with cDNA synthesis kit M-MLV version (TaKaRa). A
full-lengh cDNA library expressed specifically during the early maturation was prepared by
subtraction of the following methods. A full-lengh cDNA library from S. indicum seeds of 1 to 3
weeks old was amplified with SP6 primer, T7 primer and the PCR programme which was 16 cycles
of 98
o
C for 10 sec, 56
o
C for 5 sec and 72
o
C for 3 min, followed by 72
o
C for 3 min. They were used
as a tester cDNA in subtraction. The subtraction was carried out with DsDD cDNA subtraction kit
(Wako) using amplified cDNAs from a full-length cDNA library as a tester cDNA and cDNA materials
from young plants of four weeks after germination as a driver cDNA. Subtracted cDNA clones were
amplified with the PCR programme which was 35 cycles of 98
o
C for 10 sec, 56
o
C for 5 sec and
72
o
C for 3 min, followed by 72
o
C for 7 min. After removing cDNA clones of the lower molecular
weight with Chroma spin
TM
-200 (Clontech), they were selected in size with Chroma spin
TM
-400, and
pooled into four groups (fraction No. 4, fractions No. 5-7, fractions No. 8-14, fractions No. 15-30).
Each pooled cDNA clone was amplified with EX-taq polymerase (TaKaRa), SP6 primer, T7 primer
and the PCR programme which was 25 cycles of 98
o
C for 20 sec, 50
o
C for 30 sec and 72
o
C for 3
min, followed by 72
o
C for 5 min. They were ligated into pCR8/GW/TOPO vector (Invitrogen).

Sequence of cDNA clone
The cDNA clones from three groups (fraction No. 1-4, fraction No. 5-7, fraction No. 8-14)
were sequenced with ABI Prism
3100-Avant Genetic Analyzer (Applied Biosystems) using BigDye

terminator v3.1 cycle sequencing kit (Applied Biosystems). Homology analysis was carried out with
BLASTX (DDBJ; http://www.ddbj.nig.ac.jp/welcome-j. html ).

Transformation of Arabidopsis thaliana
The cDNA clones ligated into pCR8/GW/TOPO vector were transferred into pBI-OX-GW
(Inplanta Innovations Inc.) by using Gateway System (Invitrogen). Each cDNA clone transferred into
pBI-OX-GW was used for the transformation of Arabidopsis thaliana which was done as described
in a previous paper (Clough and Bent, 1998), with minor modification.


To obtain cDNA clones expressed specifically during the early maturation of S. indicum
seeds, the subtraction was carried out using amplified cDNAs from a full-length cDNA library from
S. indicum seeds of 1 to 3 weeks old as a tester cDNA and cDNA materials from young plants of
four weeks after germination as a driver cDNA. The subtraction efficiency was confirmed with the
PCR programme which was 22 cycles of 98
o
C for 20 sec, 50
o
C for 30 sec and 72
o
C for 1 min,
followed by 72
o
C for 3 min. The primers were GAPC-F primer (5-CCAACGCTAGCTGCACCAC-3)
and GAPC-R primer (5-AGGTCAACAACTGAGACATC-3) of the gene for cytosolic glyceraldehyde-
3- phosphate dehydrogenase (gapC) which is one of house keeping genes (Figure 1). Signals were
observed in both a full-length cDNA library from S. indicum seeds of 1 to 3 weeks old and cDNA
materials from young plants of four weeks after germination, while no signals were observed in the
subtracted cDNA library, suggesting that subtraction was efficiently performed.

th

Figure 1. Confirmation of subtraction efficiency.

The subtracted cDNA library was amplified and separated in size into four groups (fraction
No. 4, fractions No. 5-7, fractions No. 8-14, fractions No. 15-30). Fraction No. 15-30 mainly contains
cDNA clones of less than 400 bp. Therefore, 1,545 cDNA clones were sequenced from fractions
No. 4-14. Properties of cDNA clones in fraction No. 4, fractions No. 5-7 and fractions No. 8-14 were
summarized as the following; the average size 1,043.7 bp in fraction 4; 996.7 bp in fractions 5-7;
706.4 bp in fractions 8-14. The 1,545 cDNA clones were categorized and summarized with
classification of each function (Table 1). The cDNA clones responsible for protein destination
formed the largest percentage of 30.52%. Next, the cDNA clones responsible for metabolism
formed the second largest percentage of 16.36%, the cDNA clones for cell growth, division were
7.01%, the cDNA clones for transcription and RNA processing were 4.48%. Unknown and novel
cDNA clones were 30.39%. Comparison of our results with results by Suh et al. (2003) showed that
subtraction was effectively performed from the fact that the occupation percentage of house
keeping genes was low, and that of unknown novel genes was high at the present experiment. Of
them, functional analysis of nine cDNA clones: osmotin-like protein, expansin-like protein,
aquaporin-like protein, MADS-box protein 4, novel putative uncharacterized protein, ethylene
response factor 2, ethylene responsive element binding protein 3, AP2 containing transcription
factor and lipid transfer protein was carried out by overexpression of A. thaliana. Southern blot
analysis in transformed A. thaliana using each DIG-labeled sesame gene as a probe showed that
each sesame gene was indeed introduced into transformed A. thaliana (data not shown). The A.
thaliana overexpression strain for novel putative uncharacterized protein and aquaporin-like protein
showed the increase of unsaturated fatty acids in A. thaliana seeds. The amount of oleic acid per
seed grain in the overexpression strain for novel putative uncharacterized protein was 1.7 fold, and
that of linoleic acid 1.5 fold. In a strain for aquaporin-like protein, the amount of oleic acid was 1.4
fold, and that of linoleic acid 1.5 fold.

M 1 2 3
421
bp
GAPC : Cytosolic glyceraldehyde-3- phosphate dehydrogenase
GAPC
M. / Eco T14 digest
Lane 1. cDNA library from immature seeds
of 1-3 weeks after flowering
Lane 2. cDNAs from young plants
of 4 weeks after germination
Lane 3. Subtracted cDNA
th
Tabel 1. Functional category of identified genes

Function %
Protein destination 30.52
Metabolism 16.36
Cell growth, division 7.01
Transcription and RNA processing 4.48
Cell resue, defense, senescence and death 4.16
Transport 2.27
Signal transduction 2.14
Energy generation 1.10
Protein synthesis 1.04
Intracellular trafficking 0.32
Cellular organization/biogenesis 0.19
unknown 30.39

References

Budowski P. and K.S. Markley. 1951. The chemical and physiological properties of sesame oil. Chem. Rev. 48:
125-151.
Clough S.J. and A.F. Bent. 1998. Floral dip: a simplified method for Agrobacterium- mediated transformation of
Arabidopsis thaliana. Plant J. 16: 735-743.
Suh M.C., M.J. Kim, C-G Hur, J.M. Bae, Y.I. Park, C-H. Chung, C-W. Kang and J.B.
Ohlrogge. 2003. Comparative analysis of expressed sequence tags from
Sesamum indicum and Arabidopsis thaliana developing seeds. Plant Mol. Biol. 52: 1107-1123.
Satchithanandam S., M. Reicks, R.J. Calvert, M.M. Cassidy and D. Kritchevsky. 1993. Coconut oil and sesame
oil affect lymphatic absorption of cholesterol and fatty acids in rats. J. Nutr. 123: 1852-1858.
Uenishi H., T. Eguchi, K. Suzuki, T. Sawazaki, D. Toki, H. Sinkai, N. Okumura, N. Hamashima and T. Awata.
2004. PEDE (Pig EST Data Explorer): construction of a database for ESTs derived from porcine full-
length cDNA libraries. Nucleic Acids Res. 32: 484-488.

th
Effects of Different Seeding Dates on Pattern of Internode Length in
Sorghum Variety Kazetachi

Akihiro Fujii
a*
, Satoshi Nakamura
b
, Mitsuo Saito
b
,Yusuke Goto
a

a
Graduate School of Agricultural Science, Tohoku University, Sendai, Miyagi, Japan
b
School of Food, Agricultural and Environmental Sciences, Miyagi University, Sendai, Miyagi, Japan
* Corresponding author: Graduate School of Agricultural Science, Tohoku University,
1-1 Amamiya-machi, Tsutsumidori, Aoba-ku, Sendai, Miyagi, 981-8555, Japan
Tel.: +81-22-717-8639
[email protected]

Abstract

Sorghum (Sorghum bicolor Moench) stems, which have many internodes, are the main organs harvested for
feed and biofuel materials. Sorghum reportedly has three types, characterized by individual internode length
based on the internode position from base to top: 1) ever-increasing type, with internode length increasing from
the base to the top internode; 2) unimodal type, with internode length in approximately the middle internode
position that is longer than in lower or upper positions, except at the neck internode of the panicle; 3) bimodal
type, for which the internode lengths alternately increases and decreases twice before reaching the peduncle.
Sorghum variety Kazetachi, an ultralate-maturity variety in Japan with strong lodging tolerance, showed
patterns with many peaks. It is a multimodal pattern in internode length. Furthermore, this variety shows large
variation in the number of peaks per plant and the internode position with a peak among plants. This report
describes internode length pattern analysis of Kazetachi and the assessment of seeding date effects on the
pattern. Seeds were sown on 20 May, and 3 and 18 June in 2009 in the northern part of Japan. Internode
lengths were measured at harvest in early November. Peaks in the internode length pattern of each plant were
47, including both distinct and vague peaks. Pattern analysis using the internode position with a distinct peak
contributed to the distinction among patterns on each seeding date. Although internode positions showing a
distinct peak differed among patterns of different seeding dates, the period during which the internode with
distinct peaks elongated rapidly appeared to be almost identical among them, suggesting that the internode
length in Kazetachi is characterized more by environmental factors than by genetic factors.

Keywords: internode length, multimodal pattern, pattern of internode length, Sorghum bicolor Moench

Introduction

Sorghum (Sorghum bicolor Moench) stems, consisting of many internodes, are the main
organ harvested for feed and making syrup. Sweet sorghum has attracted attention recently as a
biomass energy crop because its stems accumulate large amounts of sugars, which are convertible
into ethanol: bioethanol. However, little information about development of cultivation techniques to
increase stem yield in sweet sorghum exists because most research efforts have emphasized
increasing of grain yields for grain sorghum. Stem size of sweet sorghum is the important factor that
determines the stem yield including sugar yield (Tsuchihashi and Goto 2004; Sato et al., 2008;
Nakamura et al., 2009).Increasing sweet sorghum stem yields necessitates research into internode
formation in stems. Three types of sorghum can be characterized by individual internode length
based on the internode position from the base to top (Ayyangar et al., 1938). 1) For the ever-
increasing type, the internode length increases from the base to the top internode. 2) The unimodal
type has internode length in approximately the middle internode position that is longer than in lower
or upper positions, except at the neck internode of the panicle. 3) In the bimodal type, the internode
lengths increase gradually, then decrease and increase slightly, and decrease again, with one more
increase before reaching the peduncle. However, Kazetachi, ultralate-maturity variety, with strong
tolerance of lodging in Japan, shows new patterns with many peaks: a multimodal pattern of
th
internode length. This variety also shows large variation in the number of peaks per plant and the
internode position, with the peak among plants (Figs. 1, 2) (Nakamura et al., 2011). This study
assesses a method to analyze the internode length pattern in Kazetachi and examines effects of
the seeding date on the pattern.

Figure 1. Schematic depiction of three internode length patternsthe ever-increasing, unimodal, and bimodal
typein sorghum, with the multimodal type shown for Kazetachi.

Figure 2. Short internodes among upper internodes of a stem of sorghum variety Kazetachi.


This study was conducted at the experimental field of the School of Food, Agricultural and
Environmental Sciences, Miyagi University, Japan. Seeds were sown on 20 May (S1), 3 June (S2),
and 18 June (S3) in 2009 with three replications. Seedlings were thinned to one per hill at 0.85 m
distance between the lines and to 15.0 cm between the plants. A basal fertilizer of 161416 g NPK
per m
-1
was applied. The internode length was measured for each of the 18 plants at harvest in the
beginning of November.
The (n)-th internode (IN n) was defined that between the (n+1)-th node and the (n)-th node
where the (n)-th leaf is attached. The internode position of the peak in the internode length pattern
was defined as the internode position that was longer than just upper and lower internodes.


The average of the total leaf number on the main stem was 30.7 0.1 (S1), 29.8 0.2
(S2), 29.1 0.2 (S3). Figure 3 shows the internode length of each internode position through IN8
IN28 at each seeding date. The peaks per plant in the internode length patterns shown in S1, S2,
and S3 were 35, from 36, and from 35, respectively. The average numbers of peaks were 3.6
0.2 (S1), 4.4 0.2 (S2), and 3.8 0.2 (S3) (Fig. 4). Distinct and vague peaks existin the internode
Internode position
I
n
t
e
r
n
o
d
e

l
e
n
g
t
hever-increasing type
unimodal type
bimodal type
multimodal type
th
I
II
III
length patterns of all plants, but the average patterns had very similar shapes. Three distinct peaks
were observed in the average pattern, irrespective of the seeding date (Fig. 3). According to this
result, these peaks were designated acropetally as peak I, peak II, and peak III. The respective
internode positions with peak I in S1, S2, and S3 were IN12IN14 (13.1 avg.), IN14IN17 (14.7
avg.), and IN11IN13 (12.0 avg.) (Fig. 5 and Table 1). The respective internode positions with peak
II in S1, S2, and S3 were IN20IN21 (20.4 avg.), IN18IN21 (19.4 avg.) and IN16IN20 (17.7 avg.).
The respective internode positions with peak III in S1, S2, and S3 were IN25IN27 (26.1 avg.),
IN23IN26 (24.8 avg.), and IN21IN26 (23.4 avg.). These results show that the average internode
positions of peak II and peak III shifted lower with a later seeding date, excepting peak I.

Figure 3. Internode lengths through IN8IN28 in S1 (a), S2 (b) and S3 (c).
0
5
10
15
8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32
0
5
10
15
8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32
I
II
III
c) S3
I
n
t
e
r
n
o
d
e

l
e
n
g
t
h

(
c
m
)
0
5
10
15
8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32
I
II
III
a) S1
b) S2
Internode position
th
c) S3

Figure 4. Number of internode length pattern peaks on each seeding date.

Figure 5. Internode positions with peak I peak III in S1 (a), S2 (b), and S3 (c).

0
5
10
15
10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
0
5
10
15
10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
a) S1
0
5
10
15
10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
b) S2
Internode position
N
u
m
b
e
r

o
f

s
t
e
m
0
2
4
6
8
10
12
3 4 5 6
Number of peaks per stem
N
u
m
b
e
r

o
f

s
t
e
m
S1
S2
S3
th
Table 1. Internode position and average internode position for peak I peak III for S1, S2, and S3

plot
Range of internode position Average of internode position
I II III I II III
S1 12 14 20 21 25 - 27 13.1+ 0.1 20.4+ 0.3 26.1+ 0.2
S2 14 17 18 21 23 26 14.7+ 0.1 19.4+ 0.2 24.8+ 0.3
S3 11 - 13 16 - 20 21 26 12.0+ 0.1 17.7+ 0.2 23.4+ 0.4

According to an investigation of the internodes as they increased rapidly in each plot on 5
September 2009, the positions of the internode in S1, S2 and S3 were estimated respectively as
IN20, IN19, and IN18. These internode positions correspond to internodes with peak II in each plot,
indicating that the internodes with peak II in S1, S2 and S3 were elongating at almost the same
period. These results suggest that the internode length in sorghum variety Kazetachi is
characterized more strongly by environmental factors than by genetic factors.

References

Ayyangar, G.N.R., V.P. Pao and T.V. Reddy. 1938. Studies in sorghum internodes and leaf sheaths. Proc.
Indian Acad. Sci. 7: 161-176.
Nakamura, S., N. Nakajima, A. Sato, M. Saito, Y. Nitta and Y. Goto. 2009. Accumulation of dry matter and sugar
in the stem of sweet sorghum (Sorghum bicolor Moench) after heading. Tohoku J. Crop Sci. 52: 43-44.
(in Japanese)
Nakamura, S., A. Fujii, K. Aoki, T. Tagaya, K. Hasegawa and Y. Goto. 2011. A method of analysis for the
multimodal pattern in internode length of sorghum variety Kazetachi. Jpn. J. Crop Sci. 80 (Extra issue1):
300-301. (in Japanese)
Sato, A., N. Nakajima, S. Nakamura, M. Saito, Y. Nitta and Y. Goto. 2008. Effect of fertilizer application on
characteristics of sweet sorghum (Sorghum bicolor Moench) internodes. Jpn. J. Crop Sci. 77 (Extra
issue 2): 106-107. (in Japanese)
Tsuchihashi, N. and Y. Goto. 2004. Cultivation of sweet sorghum (Sorghum bicolor (L.) Moench) and
determination of its harvest time to make use as the raw material for fermentation, practiced during rainy
season in dry land of Indonesia. Plant Prod. Sci. 7: 442-448.

th
Pranajiwa as Raw Material for Bio-Oil

Endang Yuniastuti, Susanti Indriya Wati

Agricultural Faculty, Sebelas Maret University Surakarta, Indonesia
[email protected]

Abstract

The high increase in the number of human population every year causes the increase of human need for
energy. However, it unfortunately still does not meet the production of energy sources.. This situation forces us
to seek new sources of energies which are certainly eco-friendly, such as utilization of natural resources for
biofuels. One of altenative solution is the use of Pranajiwa plants as a source for production of bio-oil. Pranajiwa
or Pranajiwa (Sterculia foetida L.) is one species of plants in Indonesia originally from East Africa, Tropical Asia
and Australia. This kind of tree crops with a kind of tall trees between 30-40 m, the tree is often found in forest.
Pranajiwa seeds contain vegetable oils that can be used as an ingredient for industrial products such as
cosmetics, soaps, shampoos, fabric softeners, paints, plastics and as an adaptive agent biodiesel. Pranajiwa
seeds contain vegetable oils comprising a fatty acid that is sterculat acid. This plant has several advantages
over other alternative crops as sources for oil production. Pranajiwa plants is not used for consumption that is
dfferent from oil palm, sugarcane, coconuts, yams or cassava that has a primary function for consumption.
Pranajiwa plants had fairly high oil yield that was greater than 40%. Event from a research conducted with the
purification using ether, the yield of oil could reach more than 70%. Whereas using direct processing, the
average oil yield rearched 45%. For biofuels, Pranajiwa seeds can then be extracted and used as raw material
of bio-oil.

Keywords: Pranajiwa, bio-oil, alternative energy

Introduction

Increase in population leds to the increase of human need for energy. The energy currently
comes from fossil and no longer it will run out. This situation encourages the Indonesian nation to
immediately provide and build a populist-based alternative energy that is environmentally friendly by
utilizing natural resources and existing plants as a source of energy that can be harnessed and
developed. One form of energy is Biofuel (BBN).
Some plants such as jatropha, sweet potatoes, cassava, sugarcane, oil palm, coconut,
sunflower, kapok, and pranajiwa or commonly known as a plant "Pranajiwa" can be developed as a
biofuel or biofuel farming and to support energy programs or green energy. , The crop plant
"Pranajiwa" (Sterculia foetida Linn.) is considered more appropriate to be used as Biofuel (BBN) or
biofuels, especially as the bio-oil (lubricating oil) and bio-diesel (diesel substitute). This is supported
by the fatty acid content which can be also used as an adaptive biodiesel.
However, the existence of plants "Pranajiwa" is now rarely found, even the presence status
of plants "Pranajiwa" included a rare (Yuniastuti, 2008). This is partly because these plants have
growing requirements at altitude less than 500 m above sea level, and exacerbated by logging and
illegal use of timber for furniture materials or raw materials made of paper without rejuvenation. The
remaining plants are only in sacred places because people are afraid to cut them down. Cultivation
of crops "Pranajiwa" is very little or not at all and eventually the plant is just a legacy from ancestors
that will be extinct. In this condition, it is necessary to give serious attention for "Pranajiwa" that has
a potential as a producer of alternative energy (bio-oil). Cultivation "Pranajiwa" can be either
generative or vegetative.
Pranajiwa (Sterculia foetida) is a kind of tree crops with high stature plants between 30-40
m, the tree is often found in the woods. Nomenclature is taken from the Roman myth, the name of
god or Sterquilinus Sterculius fertilizer. Together with the species name, foetida (meaning, hard-
smelling, foul) scientific name refers to the unpleasant odor released by these trees, especially
flowers. In some areas in Indonesia, this plant is also used as a drug. Plant leaves can be used as
an herbal remedy laxative, diuretic and mosquito deterrent; bark as a cure of some diseases; tree
wood can be used as building construction; other than edible seeds can also be used as a cough
medicine (Yuniastuti, 2010). Pranajiwa oil benefits directly related to the fatty acid content sterculat
which is unsaturated fats in seeds (Anggraeni, 2005)
th
Pranajiwa as an alternative energy-producing plant has several advantages over other
alternative energy crops, such as oil palm, sugarcane, coconuts, yams, and cassava. Pranajiwa is
not a crop for consumptions; while oil palm, sugarcane, coconuts, yams or cassava has the primary
function for consumption. Also compared to other alternative energy crops, Pranajiwa has high oil
yield that is greater than 40%, even from research conducted by refining petroleum ether the yield
can reach more than 70%. While using direct processing (compound) average oil yield reached
45%. As Fuel Plant (BBN), plant seeds and billowing retrieved and extracted can then be used as
raw material for lubricating oils (bio-oil) (Yuniastuti, 2010).

Materials and Method

Locations of research
Research locations were in 10 districts in Central Java, namely:
1. Karanganyar District: Karangmojo, Karangwuni, Derman, Ngaliyan1, Bibis, Kodokan,
Teak, Ngaliyan 2, Ngetal, Jetak
2. Sukoharjo District: Shower, Cangkol, Macanan, Temulus, Pondok 1, Pondok 2, Minggiran,
Nderso, Palur, Triyagan.
3. Boyolali District: Tegalmuncar, Klabang, Kendal big, Tlatar, Jagoan, Tagung, Badan,
Gatak Malangan, Pojok, Bulu
4. Purworejo District: Kroyo, Trukan, Doplang, Sindurjan, Tegal Kuning, Pogung Juru
Tengah, Borowetan, Bedug, Paduroso, Bayan
5. Wonogiri District: Krisak, Bulak, Godean, Donorejo, Kaloran, Nambangan, Gerdu, Brajan,
Gebang Wetan, Mblimbing
6. Klaten District: Kurung, Kalikebo, Jetis, Talang, Jerukan 1, Jerukan 2, Kebon, Sabrang,
Pandanrejo, Planggu.
7. Sragen District: Plalar, Toyogo, Bero, Pengkol, Sambung Macan, Mojopahit, Pucang,
Drojo, Tunjung Semi, Demakan.
8. Grobogan District: Gendingan, Tambirejo, Nambuhan, Bakalan, Candisari, Kepayu,
Penawangan, Getasrejo, Kronggen, Rejosari.
9. Blora District: Brengus, Dlongos, Keboan, Gagakan, Pudak, Loworejo, Jambangan, Putat,
Sukorame, Sambiroto
10. Semarang District: Ngener, Mbatan Kidul, Tawang, Reksosari, Muncar Jaten, Mrakas,
Durenan, Sambiroto, Dadapayam
Analysis of Morphology, Cytology and Molecular conducted at the Central Laboratory of the
Sebelas Maret University, Laboratory of Plant Breeding, Physiology and Biotechnology Faculty of
Agriculture, Sebelas Maret University, Surakarta.

Plant materials
Plant materials used in this study were Pranajiwa or billowing plants (Sterculia foetida
Linn.) existing in the region of Central Java which covers 10 districts of Sragen, Boyolali, Klaten,
Wonogiri, Sukoharjo, Karanganyar, Semarang, Purworejo, Grobogan and Blora.

Activities of the experiment included:
1. Identification of Morphology
2. Cytology
3. Analysis of Chemical Components
4. Seeding and In Vitro Plant Propagation Pranajiwa (Sterculia foetida Linn)


In the habitus of the plants, grendruwo is a tree with height reaching 45 meters. Plant
leaves of "Pranajiwa" grow at the end of branches, is compound leaves, and palmatus shaped
leaves with 7-8 children (foliolum). unfoliolatus-shaped leaves, long strands of leaves (laminae)
between 10-17 cm with a smooth leaf surface. Flower crop "Pranajiwa" grow at the end of branches
and branching to form clumps, and yellow to purplish red. Flower is unisexual with diameters
th
ranged between 2 2.5 cm. "Pranajiwa" Fruits are large enough with a length of about 10 cm, oval-
shaped, smooth and woody rind. Seeds of black fruit have a length of between 1.5 to 2.0 cm.
"Pranajiwa" fruits are green when still young, then become red and brown when old and will fall to
ground. "Pranajiwa" fruits are also unique and strange that are comprised of five lumps (locus),
quite large, weighing 1-3 kg that further strengthens the community,s assumption that the fruit is a
fruit of "Pranajiwa" (devil fruit). The seeds of "Pranajiwa" fruits will fall and not be utilized optimally
because many people are afraid to use it because of the above reason.
Ecologically, the "Pranajiwa" plants serve as a micro-habitat of animals and certain
animals. It is reported in Komodo Island the population of yellow-crested parrot (Cacatua subphurea
parvula) are protected and use Pranajiwa trees as a nest. "Pranajiwa" plants have crowns and
roots that are fairly large and it can function as a regulator of the hydrological cycle because the
roots can hold soil water in a large enough capacity. Internally the "Pranajiwa" plants are difficult to
breed through generative ways because its seeds have thick-though skin and dormancy (Sutopo,
2002). However, in plant nurseries soaking in warm water (temperature + 45 C) for 50-10 hours
could help to break seed dormancy (Yuniastuti, 2008). "Pranajiwa" seeds soften the harsh
experience, and can germinate 3 days after planting. In addition to the generative seed,
multiplication can also made through in vitro approaches. This is done as a form of plant germplasm
conservation of Pranajiwa. To overcome Pranajiwa from extinction, conservation efforts should be
done through both in-situ and ex situ approaches.
Morphological identification of Pranajiwa plants that were found in Central Java could be
classified into two types, namely large fruit and fruit respectively. Grouping of seeds was based on
the average weight of 10 seed parents between 1.5 to 2.0 grams (large seeds) and 1.0 to 1.5 grams
(small seeds). From the observation, the flowers appeared on the last branch or subsidiary to the
4th to the 6th. Similarly, the leaves, which also appeared in young leaves of the branch to the 4th to
the 6th. It was found that the percentage of fruit-set was quite low where in a flower stalk that
contains 20-30 flowers is only 1-2 pieces standing. In some areas the observations that had been
previously done for such research in Navan this plant was not found, it relates to altitude of the
location that is less than in accordance with the terms of Pranajiwa crops to grow. Pranajiwa grow
best at altitudes of less than 500 m above sea level. Meanwhile, in some locations of Semarang
regency Pranajiwa also have not been found anymore because it was felled and no effort for the
rejuvenation of this plant has been done.
Observations in some locations in Blora and Grobogan District Pranajiwa plants have been
started to be used for reboitation by the District Government and Blora through the Grobogan
Department of Public Works (MPW) by planting plants on the curb and the edge of the irrigation
channels.
In May to July pranajiwa plants begin to form flowers and young fruits become old fruit,
which is ready for harvesting. In general, pranajiwa plants flowering and fruiting are throughout the
year. This situation allows pranajiwa plants to be intensively cultivated and used as biofuel
feedstock (bio-oil).
Observation of pranajiwa chromosome number indicated that the number of chromosomes
is 2n = pranajiwa 2X = 32. This number gives the assurance that the number of pra
najiwachromosomes is 32 not 40. The number of chromosomes is reinforced by images of cells of
different pranajiwa (Setyawan, 2009) The previous opinion that pranajiwa chromosome number was
40 may be due to that the number of chromosomes of the genus Sterculia is 40 (six of nine species
of the genus Sterculia species that have been identified and has a number of chromosome 40 is S.
acerifolia A. Cunn., S. A. St Chicha .- Hil., S. rubiginosa Vent., S. striata A. St .- Hil., S. urens Roxb.,
and S. villosa Roxb.). another reason is that the method used by previous researchers was less
precise that might cause a low quality of the picture of chromosome (eg cell rupture that resulted in
the chromosomes of neighboring cells join counted that made the chromosome number increased).
Karyotype was based on chromosome length, and shape of chromosomes. Based on the
similarity of the size and shape of chromosomes could be seen that pranajiwa chromosomes are
diploid. Based on the size and curve of the centromere is known that each pair of chromosomes
pranajiwa is two. This is supported by the similarity of the size and shape of a sorted chromosomes
that are homologues of each chromosome.
Standard chemical analysis consisting of analysis of terpenoid compounds, flavonoids, and
steroids showed a very low content even not exist at all. Further analysis for tannins, saponins and
alkaloids also showed a very low content. This could facilitate the purification pranajiwa seed oil as
th
a lubricating oil feedstock (bio-oil). Common proximate analysis consisted of water, fat content,
protein, carbohydrate, ash, and others.
To determine the amount of oil content (yield results) seeds was carried by two methods
that are compress (compound) and of purification with ether methods. On purification with ether, oil
content (yield results) was obtained nearly 70%. While the direct compression method yield the
results was obtained about 40%. High oil yield from pranajiwa seeds indicate a huge potential for
further development as a lubricating oil (bio-oil).

References

Anggraini, L. 2005. Karakteristik Produk Hidrogenasi Ester-Ester (Monoalkil) Asam-Asam Lemak Minyak
Pranajiwa ( Sterculia foetida Linn.) sebagai Adaptif http://abstraksi-ta.itb.ac.id./abstraksi-1&detail-1&id-
760& tahun-2005 Pada hari Senin, 20 Nopember 2006.
Setyawan, B. 2009. Analisis Sitogenetika Tanaman Pranajiwa ( Sterculia foetida L). Skipsi S1. Fakultas
Pertanian Universitas Sebelas Maret.Surakarta.
Sutopo, L. 2002. Teknologi Benih . Rajawali. Jakarta.
Yuniastuti. 2008. Identifikasi dan Seleksi Keragaman Tanaman Pranajiwa ( Sterculia foetida Linn.) Serta
Teknologi Perbanyakan Tanaman Secara In Vitro Untuk Penyediaan Bahan Baku Biofuel. Laporan
Penelitian Riset Insentif Dasar. Kementrian Ristek. Universitas Sebelas Maret. Surakarta.
-----------. 2010. Identifikasi dan Seleksi Keragaman Tanaman Pranajiwa (Sterculia foetida Linn).
http://lppm.uns.ac.id. Diakses pada Rabu, 15 September 2010. 2010.

th
th
Selection and Evaluation Characteristics of Six Candidate Varities of
Cucumber (Cucumis sativus) in the Dry Season Planting

Rahayu, S.T
a,
*, U.Sumpena
a
, Ali Asgar
a

a
Indonesian Vegetables Research Institute (IVEGRI)
* Corresponding author: Indonesian Vegetables Research Institute (IVEGRI)
Jl.Tangkuban Perahu no 517 Lembang, Bandung
Tel.: 0222786245; fax: 0222786416.
[email protected]

Abstract

Cucumber is one of vegetables that are rich in vitamin C. The purpose of this study was to select and to
evaluate physical and chemical characteristics of six varieties of cucumber that will be released as new varieties.
Planting sited was chosen in plain medium during the dry season in Bandung. The design used was randomized
block design with three replicates. Observation was done by determining physical characteristics including
length, diameter, weight, texture, and colour of fruit. Chemical characteristics observed were moisture and
content of vitamin C. The results showed that two varieties were not significantly different from the
characteristics of the control, so both can be recommended to be released as new varieties.

Keywords: characteristics, cucumber, selection, varieties.

Introduction

Cucumber (Cucumis sativus) is one type of vegetable widely grown in Indonesia.
Cucumber has a fairly broad market both modern and traditional markets. Cucumber production in
Indonesia in 2009 reached 583,139 tons per hectare with an area of 56,099 hectares planted.
Production mostly in West Java, Central Java and North Sumatra provinces (Anonymous, 2010).
Production is still potential for further improved.
Cucumber planted in low, medium, or high plains with optimal rainfall ranges between 200-
400 mm/month. Too high rainfall is not suitable for growing vegetables, as it will abort flowers
(Sumpena, 2007). Cucumber grow well at the acidity of the soil ranged from 5.5 to 6.5, on alluvial,
latosol, and andosol soil type. Cucumber planted in the lowlands can be harvested faster than
cucumbers grown in the highlands. Cucumber harvest age ranged from 30 to 50 days after planting
(Arief, 2009). Cucumber is one of horticultural commodity easy to handle because it is grown with
simple maintenance, inexpensive, and short-lived cycle when it is compared to other vegetables
such as tomatoes or peppers. Fluctuations in market prices are low compared to other vegetables,
so it would be more profitable for farmers (Sumpena, 2007).
Cucumbers can be consumed directly in fresh as a salad and for pickles. The slicing
cucumber are peeled, sliced and served with vinegar or dressing or as an ingredient of salads. In
South-East Asia, the young shoots are eaten as raw or steamed (Siemonsma and Piluek, 1994).
Cucumber is very important in South East Asia as it is in temperate regions. Breeding work should
be aimed to produce improved cultivars resistence to diseases and pests attack in tropical lowland
condition (Siemonsma and Piluek, 1994).
The nutrient content per 100 grams of cucumber is water at 96 g, protein at 0.6 g, fat at 0.1
g, carbohydrates at 2.2 g, Calcium at 12 mg, Iron at 0.3 mg, vitamin C at 12 mg. Cucumber fruit
consists of 24 mg of P, 45 IU of Vitamin A, 0.03 mg of Vitamin B1, 0.02 mg of Vitamin B2, 0.3 mg of
Niacin, and 15 mg at magnesium, respectively (Siemonsma and Piluek, 1994). In addition,
th
cucumber are also rich in fiber. The purpose of this study was to select and to evaluate physical and
chemical characteristics of six varieties of cucumber that will be released as new varieties.


The research was conducted in plain medium during the dry season at Ciwastra, Bandung
400-700 m above sea level. Chemical analysis was performed at the laboratory of plant physiology
at IVEGRI in Lembang, Bandung. Materials used in this experiment were three candidates of new
varieties and three varieties of cucumber production of private firms as control.
Each treatment was planted in mulched beds at 9,6 m
2
using a plant distance of 40 x 60
cm. The fertilizer applied was NPK at 125 kg/ha and goat manure at 20 ton/Ha. The remaining dose
given as a supplementary fertilizer twice during the plant growth. To control pests of plants (OPT)
pesticides were used intensively twice a week, starting at two weeks after planting. Pesticides were
adjusted to the type of pests that attacked.
Research was carried out by Randomized Design Group consisted of three replicates.
Observation physical parameters included length, diameter, weight, colour, and texture of the fruit.
Chemical parameters measured were moisture and vitamin C. Texture observation was done using
a QTS 25 Texture Analysis, and colour observations used a chroma meter. Statistical tests were
performed with the PKBTSTAT analysis followed by Tukey test at 5% level.


There are two types of cucumbers were observed in this study, i.e. green and white
cucumbers. Green cucumber fruit is longer than the local cucumbers. Table 1 shows that the
varieties of fruit length of variety H1 was not significantly different with the comparison varieties H5.
Varieties H2, H3, and H4 were not significant different.

Tabel 1. Analysis variance for length, diameter, weight,colour, texture of cucumber fruit, moisture, and vitamin C
of six virieties

Variety
Length
(cm)
Diameter
(cm)
Weight
(g)
Colour
(N/mm)
Texture
(mm/10sec/50g)
Moisture
(%)
Vitamin C
(mg/100g)
H1 20.89
a
3.37
b
121.47
a
0.89
b
0.12
ab
95.30
b
19.16
b

H2 16.53
b
3.87
a
146.70
a
0.93
b
0.12
ab
95.68
a
17.87
c

H3 14.43
bc
4.22
a
150.44
a
1.05
a
0.14
a
95.14
b
19.06
b

H4 16.44
b
3.93
a
144.98
a
0.94
b
0.14
a
95.38
ab
17.28
c

H5 21.27
a
3.27
b
140.83
a
0.89
b
0.10
b
94.49
c
20.06
a

H6 12.66
c
3.83
a
145.63
a
1.05
a
0.12
ab
95.66
a
17.86
c

HSD 5% 2.19 0.40 71.08 0.10 0.03 0.31 0.79

Table 1 also shows that the diameter of varieties H1 was not significantly different with H5,
meanwhile among varieties H2, H3, and H4 were not significantly different. Diameter would affect
the weight of fruit. Type of fertilizer affect the production of cucumber (Sutater and Supriyadi, 1989).
Cucumber weight of six varieties were not significantly different at level 5% at Turkey test.
Cucumber weight affected the total production of cucumber. Factors planting and type of fertilizer
used affected plant growth and produced cucumber (Hilman and Rosliani, 2004). Irigation and
composition of the N on the fertilizer also affected the weight of cucumber (Zhan et al., 2011).
th
The colour of varieties H1, H2, H4, and H5 were not significantly different from each other,
they were more dominant to the colour of green. Variety H3 was not significantly different compared
with variety H6, having the dominant colour of white. Cucumber colour ranges from dark green,
green, light green, whitish green to white depending on the type varieties (Sumpena, 2007).
Texture of varieties H1, H2, and H6 were not significantly different among them. Similar
results were also found for varieties H3, H4, and H5. Higher texture value indicated softer texture,
and conversely lower texture values indicated tougher texture. Texture value difference was also
influenced by varieties and fertilization. K elements made harder texture, while the elements of N
make the texture softer (Wiranatakusumah et al, 1992). Texture of consumer software was not
preferred. Storage temperature affected the texture of the cucumber. Storage at low temperature
will maintain the texture of the cucumber (Kohyam et al, 2009).
The highest moisture content was found in the variety H2, while the lowest was found at
variety H5. Variety H1 was not significantly different compared with variety H3. Moisture will affect
the shelf life of these products. The presence of water in food is a good medium for the growth of
microorganisms. The high moisture is held within the product by osmotic force within cells, mostly
as free water, althought a small proportion is chemically bound, therefore, this is more tightly held
and more stable (Will, et al., 1989). Variety H5 had the highest of Vitamin C content , while variety
H4 was the lowest. The vitamin C in vegetables is affected by the type of varieties and types of
seasons. In the rainy season Vitamin C content is higher level compared with in the dry season
(Hanson et al, 2011).

Conclusions

Caracteristic cucumber was effected by the kind of varieties. Varieties H1 and H3 had
good caracteristics to be released in public, because they had low moisture and high in the Vitamin
C content.

References

Anonymous, 2010. Statistik Indonesia. Biro Pusat Statistik. Jakarta.Pp.220-225
Appel LJ, Moore TJ, Obarzanek E .1997. A Clinical Trial of the Effects of Dietary Patterns on Blood Pressure.
DASH Collaborative Research Group. J Med.16:1117-1124.
Arief P.S., 2009. Agribisnis Mentimun. Penerbit CV.Pustaka Grafika, Bandung.Pp. 1-34
Hanson, P., et al, 2011. Carotenoids, ascorbic acid, minerals, and total glucosinolates in choysum (Brassica
rapa cvg. parachinensis) and kailaan (B. oleraceae Alboglabra group) as affected by variety and wet and
dry season production. Journal of Food Composition and Analysis. Article in Press.
Zhan H-X, D-C Chi, Q Wang, J Fang, and X-Yu Fang.2011. Yield and Quality Response of Cucumber to
Irrigation and Nitrogen Fertilization Under Subsurface Drip Irrigation in Solar Greenhouse. Agricultural
Sciences in China. 10 (6) :921-930.
Hilmam, Y and Rosliani, R. 2004. Pemanfaatan cacing tanah untuk meningkatkan kualitas hara limbah organik
dan hasil tanaman mentimun. Jurnal Hortikultura 12(3): 148-157.
Kohyam ,K., A Nagata, Y Tamaki, and N Sakurai. 2009. Postharvest Biology and Technology. 53(2): 243-246
Siemonsma, J.S., and Piluek, K.1994. Plant Resources of South-East Asia 8 Vegetables. Prosea Foundation .
Bogor, Indonesia. 157-160
Sumpena, U 2007. Budidaya Mentimun Intensif dengan Mulsa, Secara Tumpang Gilir. Penebar Swadaya.
Jakarta.Pp 16-17
Sutater, T and Supriyadi, A., 1989. Pengaruh pemberian kapur pertanian, pupuk kandang dan P terhadap
produksi mentimun di tanah latosol masam. Bul.Penel.Hortikultura XVIII(3): 27-32.
Will, R.B.H., McGlasson, W.B., Graham, D., Lee,T.H., 1989. Postharvest. An Introduction to Physiology and
Handling of Fruit and Vegetables. An Avi Book. Van Nonstrand Reinhold.New York. Pp 53-56.
Wiranatakusumah, M.A., Abdullah, K, Syarief, AM. 1992. Sifat Fisik Pangan. PAU IPB. Bogor. Pp 225 -232.
th
Blue Light Induced the Stem Growth in Vegetable Water Spinach

Futoshi Sasaki
a,*
, Mikio Sekinuma
a
, Futoshi Kato
b
and Naoto Inoue
b

a
Interdisciplinary Graduate School of Science and Technology, Shinshu University, Minamiminowa, Japan
b
Faculty of Agriculture, Shinshu University, Minamiminowa ,Japan.
Tel.: +81 265 77 1314.
[email protected]

Abstract

A local variety of water spinach in Taiwan was grown under various artificial light conditions to clarify the suitable
growth condition in a plant factory. In this experiment, water spinach shoots were grown under various artificial
light spectra controlling plant growth. Eight plots with conditions of 8 different light qualities were used to
compare the growth of the water spinach plant. Different light qualities were established by combining 3 types of
fluorescent light selected from 4 types of light emitted by white, blue, purplish-red, and far-red fluorescent lamps,
respectively, and irradiation treatments were performed for 10 days in each plot. The results showed that the
plant length and stem diameter increased in the plot in which 1 white and 2 blue fluorescent lamps were set.
Increase in plant length and stem diameter were positively correlated with the energy of blue light (400-480 nm),
but were negatively correlated with energy of green, red and far-red light (520-780 nm). The size of the stem
cavity negatively correlated to the amount of energy of red light (600-660nm) and positively correlated to the
amount of energy of blue light (480 nm). The results suggest that blue light promotes and red light inhibits stem
growth of the water spinach.

Keywords: artificial light, light quality, plant length, stem diameter, water spinach

Introduction

Water spinach (Ipomoea aquatica Forsk.) is a popular vegetable in Japan because of its
good texture and high nutrient value. This vegetative has a high content of protein (2.2 g/100 g),
calcium (74 mg/100 g) and fiber (3.1 g/100 g) (JATCC, 2009). Moreover, many researchers have
evaluated the chemical characteristics of this functional food (Miean and Mohamed, 2001; Prasad
et al., 2005; Dasgupta and De, 2006). However, the duration of cultivation of this plant is limited to
summer because the frost resistance of this plant is low. For obtaining a stable yield throughout the
year, water spinach must be cultivated in an artificial environment that provides suitable conditions
for its growth. The species can grow easily in hydroponic cultures, and it shows a high nutrient
absorption. Therefore, the best growth conditions (light, temperature, nutrition) required for this
species must be investigated in detail to maximize the production and sales of this vegetable. In this
experiment, the light spectra that controls stem growth were investigated to establish a year-round
culture under low energy input condition.


Plant materials
A local variety of water spinach from Taiwan was used in this indoor experiment. The
seeds were scarified and soaked in water for 3 days, and the germinated seeds were sown on
culture soil in 12 cm poly pot. After sowing, the seedlings were grown under the light of fluorescent
lamps (FL40SBR-A, NEC Co. Ltd., Japan) for 7 days. After 7 days, we removed these fluorescent
lamps and set other fluorescent lamps producing different light colors, therefore, these seedlings
were grown under different light quality conditions by using artificial light.
th
Treatments and analytical method
Four different fluorescent lamps (white, blue, purplish red and far red) were used in
different combinations to provide different lightings in 8 plots (L1-L8). Fig.1 shows the light spectrum
of the 4 fluorescent lamps. The spectral distribution of the light in each plot was measured with a
spectroradiometer (HSU-100S, Asahi Spectra Co. Ltd., Japan). Table 1 shows the energy
distribution in each spectral band (UVA, B, G, R and FR). The air temperature was maintained at
27C in the room, and all fluorescent lamps were continuously irradiated. The photosynthetic photon
flux density (PPFD) was adjusted to 200 mol m
-2
s
-1
at the top of the seedlings in each plot. Ten
days after the treatments, the main stem length, stem diameter and cavity size were measured
(Figure 2), and the average of all these parameters were calculated from the data of 15 stems.
The correlations between the morphological traits of the stems and the light quality in each
plot were obtained. The analytical method of statistics referred to Kasajima et al. (2007). The ratio
of energy (RE) was defined as the light energy in a specified wavelength width (50 nm) to the total
light energy in the whole spectral range (250-1000 nm).

0
0.2
0.4
0.6
0.8
1
1.2
1.4
1.6
300 400 500 600 700 800
E
n
e
r
g
y

d
e
n
s
i
t
y
W

c
m
-
2

n
m
-
1
Wavelengthnm
B
W
PR
FR

B = Blue (Caribbean Blue, 15W, Sudo Co. Ltd., Japan), W = White (Mellow White, 15W, Toshiba Co. Ltd., Japan), PR = Purplish
red (Exotic Rose, 15W, Sudo Co. Ltd., Japan),
FR = Far-red (FL20SFR74, 20W, Toshiba Co. Ltd., Japan)

Figure 1. The emission spectra of four kinds of fluorescent lamps used in the experiment.

Table 1. The light quality in experimental plots (L1-L8)

UVA B G R FR
L1 W + W + W 0.018 0.314 0.457 0.182 0.020
L2 W + PR + PR 0.007 0.410 0.351 0.220 0.010
L3 W + B + B 0.007 0.697 0.224 0.051 0.004
L4 W + PR + B 0.007 0.523 0.317 0.132 0.011
L5 W + W + FR 0.010 0.263 0.345 0.146 0.188
L6 W + PR + FR 0.005 0.302 0.307 0.155 0.210
L7 W + B + FR 0.010 0.390 0.265 0.090 0.204
L8 PR + B + FR 0.004 0.491 0.183 0.139 0.170
Plot
Combination of lamps
1)
RE in each spectral region
2)

1) Refer to Figure 1.
2) Ratio of energy in UVA (320-400nm), B(400-500 nm), G(500-600 nm), R(600-700 nm) and FR (700-800nm) range to
that in whole spectral range (250-1000 nm).

th

a, Stem diameter, b, Cavity size

Figure 2. Stem-cross section in water spinach.


The plant length and stem diameter of water spinach increased in the plot in which 1 white
and 2 blue fluorescent lamps were set (L3 in Table 3). Figure 3 shows the correlation coefficient
between REs in various spectral ranges and the morphological traits of stems. Plant length and
stem diameter were positively correlated with the energy of blue light (400-480 nm), however, they
had negative correlation with the energies of green, red and far-red lights (520-780 nm). In
particular, stem diameter was significantly correlated with the energies of light at wavelengths of
480 nm and 660 nm. The size of the stem cavity was negatively correlated to the amount of energy
of red light (600-660nm) and positively correlated to the amount of energy of blue light (480 nm).
These results showed that the stem diameter, stem length and cavity size growth were
promoted by blue light and inhibited by red light. Blue light had a positive effect on the stem growth
of water spinach cultivated under artificial light conditions. However, some studies showed different
results. Minanizawa and Kitta (1977) reported that greenish blue light of 450-550 nm suppressed
the growth of mulberry (Morus alba L.). In morning glory (Ipomoea nil L), the elongation of plant
length decreased under the blue light compared with that under green or red lights (Yamazaki et al.,
2003). Kasajima et al., (2008) reported that red and green light play an important role in regulating
hypocotyl elongation in common buckwheat (Fagopyrum esculentum Moench) and Tartary
buckwheat (Fagopyrum tataricum Gaertn.). In petunia (Petunia hybrid Vilm.), blue light had no
effect on the plant height (Fukuda et al., 2002). These reports suggested that the light response
systems of some plants differed from those of water spinach.
On the other hand, stem elongation of eggplant (Solanum melongena L.) and sunflower
(Helianthus annuus L.) were promoted under blue light (Hirai et al., 2006). Goto (2003) summarized
the findings of previous studies in order to evaluate the significant effects of the quality of artificial
light on plant growth and reported that blue light had various effects on plant growth. Therefore,
these reports and our results suggest that the effects of light quality on stem growth differed among
plant types and species. In future, these factors should be studied in detail for controlling the plant
growth under artificial light.
th
-1
-0.8
-0.6
-0.4
-0.2
0
0.2
0.4
0.6
0.8
1
400 500 600 700
C
o
r
r
e
l
a
t
i
o
n

c
o
e
f
f
i
c
i
e
n
t

Wavelength nm
-1
-0.8
-0.6
-0.4
-0.2
0
0.2
0.4
0.6
0.8
1
400 500 600 700
C
o
r
r
e
l
a
t
i
o
n

c
o
e
f
f
i
c
i
e
n
t

Wavelength nm
-1
-0.8
-0.6
-0.4
-0.2
0
0.2
0.4
0.6
0.8
1
400 500 600 700
C
o
r
r
e
l
a
t
i
o
n

c
o
e
f
f
i
c
i
e
n
t

(
r
)
Wavelength (nm)
Stem diameter
Main stem
length
Cavity size

Significant level: |r| > 0.83 (p < 0.01)

Figure 3. Correlation coefficient between RE in various spectral ranges and morphological traits of stem.

References

Nabasree D and B De 2007. Antioxidant activity of some leafy vegetables of India: A comparative study. Food
Chem. 101: 471-474.
Naoya F, M Kobayashi-Yoshinaka, M Ubukawa, K Takayanagi and S Sase 2002. Effects light quality, intensity
and duration from different artificial light sources on the growth of petunia (Petunia hybrida Vilm.). J.
Japan. Soc. Hort. Sci. 71:509-516
Eiji G, 2003. Effects of light quality on growth of plants under artificial lighting. Environ. Control in Biol. 41: 121-
132.
Tadayoshi H, W Amaki and H Watanabe 2006. Effects of monochromatic light irradiation by LED on the
internodal stem elongation of seedlings in eggplant, leaf lettuce and sunflower. J. SHITA. 18: 160-166.
(In Japanese, with English abstract)
JATCC 2009. Standard Tables of Food Composition in Japan. Pp305.
Shin-ya K, N Inoue, M Shirai, R Mahmud and K Fujita 2008. Effect of various light qualities on hypocotyl
elongation in common and tartary buckwheat. Fagopyrum. 25: 37-43.
Shin-ya K, N Inoue, R Mahmud, K Fujita and M Kato 2007. Effect of light quality on developmental rate of wheat
under continuous light at a constant temperature. Plant Prod. Sci. 10: 286-291.
Koo MH and S Mohamed 2001. Flavonoid (myricetin, quercetin, kaempferol, luteolin, and apigenin) content of
edible tropical plants. J. Agric Food Chem. 49: 3106-3112.
Kichisaburo M and F Kitta 1978. Effect of light quality on the growth of mulberry. J. Sericult. Sci. Japan. 47: 9-14.
(In Japanese, with English abstract)
Nagendra PK, S Divakar, GR Shivamurthy and SM Aradhya 2005. Isolation of a free radical-scavenging
antioxidant from water spinach (Ipomoea aquatica Forsk). J. Sci. Food Agric. 85: 1461-1468.
Keisuke Y, Y Isii, S Matsui and I Tanaka 2003. Effects of light quality, daylength, and growing temperature on
flowering in morning glory (Pharbitis nil Choisy). Environ. Control in Biol. 41: 211-219.

th
Effects of Genotypes and Storage Time on Quality Parameters of
Chinese Flowering Cabbage (Caisim) Planted in Subang

Rahayu,S.T.
a*
R.Kirana
a

a
Indonesian Vegetables Research Institute (IVEGRI)
Jl.Tangkuban Perahu no 517 Lembang Bandung 40391
* Corresponding author: Jl.Tangkuban Perahu no 517 Lembang, Bandung, Indonesia
Tel.: 0222786245; fax: 0222786416.
[email protected]

Abstract

Chinese flowering cabbage (Brassica rapa parachinensis) is one type of leaf vegetables which are rich in fiber,
minerals, and vitamins. Postharvest handling techniques and storage will affect the quality of chinese flowering
cabbages. This experiment aimed to determine the effect of variety and storage time on quality parameters of
chinese flowering cabbages. Chinese flowering cabbage was planted in Subang. The experiment was designed
using Randomized design group (RAK) with three replications and two factors. The first factor was variety
consisting of 10 varieties and the second factor was storage time were 5 and 10 days. Observations were made
on 0, 5, and 10 days. Chinese flowering cabbage was placed in a cold storage at a temperature of 10
o
C with
humidity at 98%. Observing parameters included texture, colour, moisture, ascorbic acid, fiber, and chlorophyll
content. The results showed that three varieties on storage for 5 days had good quality parameters.

Keywords: chinese flowering cabbages, quality, storage time, variety

Introduction

Chinese flowering cabbages that is one type of leaf vegetables grows well in Indonesia.
Chinese flowering cabbage production and other types of mustard in 2009 were 562.838 tons with a
planting area of 56,414 hectares. The plants are most widely grown in West Java, Central Java and
North Sumatra provinces (Anonymous, 2010).
There were 22 varieties of chinese flowering cabbages or caisim that have been released
by private sectors through introduction. Eventhough IVEGRI has not released any variety of chinese
flowering cabbages, the seeds of chinese flowering cabbages line (LV-145) have been distributed to
users. LV-145 already has a uniform appearance, but its quality has not been documented well.
Chinese flowering cabbages contain many vitamins and minerals that essential are for our
body needs. The nutrient content per 100 gram edible fresh portion moisture 95 g, protein 1.2 g, fat
0.2 g, carbohydrates 1.2 g, vitamin A 5800 IU, vitamin B1 0.04 mg, Vitamin B2 0.07 mg, Niacin 0, 5
mg, ascorbic acid 53 mg, 102 mg Ca, Fe 2 mg, mg 27 mg, P 37 mg, K 180 mg, Na 100 mg. The
brassica family includes broccoli, cabbage, kale, cauliflower and brussels sprouts, to prevent many
common diseases such as cancer, heart disease, diabetes and hypertension (Siemonsma and
Piluek, 1994).
The purpose of storage to maintain the price stability, inhibit the development of biological
agents and preserve the quality of the produce in minimal moisture of loss and reduce the
respiration (Dris et al.,2003).
The purpose of this experiment was to determine the quality of LV-145 and other chinese
flowering cabbages line as a preliminary testing.

th

The preliminary testing of chinese flowering cabbage quality was conducted in IVEGRI
Research Station in Subang, 100 m above sea level. The treatments were 10 genotypes (five
IVEGRI line and five released varieties as control). The experiment was designed using
Randomized Design Group (RAK) with three replications. Differentiation among treatments to
determine (genotypes) using the F test at 5% level of test. If there was a significant the analysis was
continued using LSD test. Plants were grown in mulched beds measuring 3m
2
using a plant
distance of 20 cm x 20 cm with a population of 60 plants for each replication. The first application of
fertilizers given were goat manure (10t/ha) and half dose of NPK 16:16:16 (1.5 t/ha). The remaining
dose of NPK was given twice as a supplementary fertilizer during the plant growth. In addition, lime,
dolomite (1 ton/ha), was applied a week before planting. Pesticides were applied twice a week to
control pests, starting two weeks after planting. Pesticides were adjusted to the type of pests that
attacked.
Chinese flowering cabbages were kept in cold storage at a temperature of 10
0
C with RH
98%. Observations were conducted on 0, 5 and 10 days. Physical and chemical analyses were
conducted in IVEGRI Laboratory. Physical analysis covered texture and colour, while chemical
analysis included moisture, ascorbic acid, chlorophyll content, and fiber.


Table 1. Analysis of variance of texture, colour, moisture, ascorbic acid,chloropyll, and fiber for genotype

Genotype
Texture
(mm/sc/gr)
Colour
(N/mm)
Moisture
(%)
Ascorbic acid
(mg/100gr)
Chlorophyll
(g/mg)
Fiber
(%)
1 2.07
a
1.18
a
92.37
c
93.94
d
262.42
cd
0.99
ef

2 2.08
a
1.21
a
92.36
c
94.12
d
216.63
d
1.10
d

3 2.02
a
1.26
a
92.97
a
81.74
g
232.05
d
1.18
c

4 2.05
a
1.20
a
93.13
a
87.04
f
245.84
cd
1.14
cd

5 2.03
a
1.23
a
92.60
b
92.72
d
340.11
b
1.38
a

6 2.02
a
1.13
a
92.27
c
90.25
e
376.50
b
1.00
ef

7 2.16
a
1.23
a
92.74
b
86.27
f
245.74
cd
0.96
f

8 2.00
a
1.22
a
92.66
b
96.19
c
282.82
c
1.04
e

9 2.04
a
1.20
a
92.18
c
106.62
b
347.62
b
1.32
b

10 2.09
a
1.21
a
91.39
d
112.24
a
538.55
a
1.36
ab

HSD 5% 0.30 0.16 0.21 1.84 50.17 0.05

Table 2. Analysis of variance of texture, colour, moisture, ascorbic acid, chlorophyll, and fiber for storage time

Storage Time
Texture
(mm/sc/gr)
Colour
(N/mm)
Moisture
(%)
Ascorbic acid
(mg/100gr)
Chlorophyll
(g/mg)
Fiber
(%)
0 hari 1.81
b
0.89
c
92.10
b
77.43
c
53.99
c
0.98
c

5 hari 1.91
b
1.25
b
93.41
a
85.80
b
498.70
a
1.00
b

10 hari 2.45
a
1.49
a
91.89
c
119.11
a
373.79
b
1.46
a

HSD 5% 0.12 0.06 0.08 0.73 19.88 0.02
th

Figure 1. Effect of genotypes on chinese flowering cabbage texture.

Figure 1, the hardest texture was shown by genotype number 6, while the value of the soft
texture was shown by genotype number 7. However, from the results of LSD test at 5% level shows
that there is no significantly different for all varieties (Table 1). Duration storage affected the texture
of chinese flowering cabbage. This was indicated by the value of texture where 5 days storage was
significantly different from 10 days storage (Table 2). The longer storage time, the more evaporation
from the material occurs that is due to the process of respiration.

Figure 2. Effect of genotypes on chinese flowering cabbages colour.

Figure 2 shows that genotype number 6 had the lowest value of the colour (dark green),
whereas genotype number 3 had the highest colour value (light green).However, the test of LSD at
the level of 5% all types of varieties were not significantly different in colour values. The colour
influenced by the content of chlorophyll is one of the parameters that affect the appearance of the
product. Genotype number 3 had lower chlorophyll content than genotype number 6. Furthermore,
colour values were significantly different for 0, 5 and 10 days-storage. During storage, chinese
flowering cabbage colour changes because the process of respiration continues. Table 3 shows the
genotypes no 3,4, and 5 were not significantly different from control genotypes number 9 and 10 for
the colour values in 5 days-storage.
th
Table 3. Texture, colour, moisture, ascorbic acid, chlorophyll, and fiber for storage time * genotype

ST*Var
Texture
(mm/sc/gr)
Colour
(N/mm)
Moisture
(%)
Ascorbic acid
(mg/100gr)
Chlorophyll
(g/mg)
Fiber
(%)
ST 0 D VAR1 1.79
ghij
0.89
e
92.68
cd
76.34
kl
45.91
k
0.92
jklm

ST 0 D VAR2 1.73
hij
0.90
de
92.06
fghij
78.44
jk
54.67
k
0.97
jkl

ST 0 D VAR3 1.72
ij
0.91
cde
92.55
cde
73.19
lmno
43.27
k
0.85
mno

ST 0 D VAR4 1.74
hij
0.89
e
92.81
c
72.36
mno
41.44
k
0.90
jklm

ST 0 D VAR5 1.81
fghij
0.89
e
91.78
ijk
88.36
h
50.89
k
1.01
ij

ST 0 D VAR6 1.91
bcdefghij
0.87
e
91.72
ijk
67.34
p
58.06
k
0.95
jklm

ST 0 D VAR7 1.91
bcdefghij
0.88
e
91.68
ijk
76.34
kl
55.91
k
0.96
jklm

ST 0 D VAR8 1.81
fghij
0.89
e
91.90
ghijk
75.24
klmn
57.46
k
0.98
ijk

ST 0 D VAR9 1.89
cdefghij
0.87
e
92.23
efgh
81.44
ij
59.18
k
0.88
klm

ST 0 D VAR10 1.75
hij
0.88
e
91.62
kl
85.22
hi
73.14
k
1.35
de

ST 5 D VAR1 1.88
defghij
1.24
abcd
91.82
hijk
97.25
g
551.44
de
1.08
hi

ST 5 D VAR2 2.17
abcdefghij
1.24
abcd
93.88
b
71.63
no
339.03
ghi
0.77
no

ST 5 D VAR3 1.84
efghij
1.29
ab
94.05
ab
72.68
lmno
393.23
fg
1.21
fg

ST 5 D VAR4 1.97
abcdefghij
1.27
ab
94.32
a
75.82
klm
375.21
fgh
0.94
jklm

ST 5 D VAR5 1.84
efghij
1.27
ab
94.02
ab
84.71
hi
577.60
cd
1.33
de

ST 5 D VAR6 1.64
j
1.12
bcde
93.88
b
71.11
op
410.63
fg
0.75
o

ST 5 D VAR7 2.04
abcdefghij
1.24
abcd
93.72
b
75.81
klm
409.41
fg
0.59
p

ST 5 D VAR8 1.81
fghij
1.25
abc
93.72
b
83.14
i
457.04
ef
0.87
lmn

ST 5 D VAR9 1.92
bcdefghij
1.26
ab
92.65
cde
100.91
g
629.84
bcd
1.19
gh

ST 5 D VAR10 2.02
abcdefghij
1.29
ab
92.08
fghi
124.96
d
843.56
a
1.30
def

ST 10 D VAR1 2.55
a
1.40
ab
92.63
cde
108.24
f
189.89
j
0.96
jklm

ST 10 D VAR2 2.35
abcdefgh
1.48
a
91.15
m
132.28
b
256.19
ij
1.56
b

ST 10 D VAR3 2.50
abcd
1.56
a
92.31
defg
99.35
g
259.65
ij
1.47
bc

ST 10 D VAR4 2.45
abcde
1.44
ab
92.27
defg
112.94
e
320.86
ghi
1.58
b

ST 10 D VAR5 2.43
abcdef
1.54
a
92.00
fghijk
105.10
f
391.84
fg
1.79
a

ST 10 D VAR6 2.49
abcd
1.42
ab
91.20
lm
132.29
b
660.82
bc
1.31
def

ST 10 D VAR7 2.52
ab
1.55
a
92.81
c
106.67
f
271.89
hij
1.33
de

ST 10 D VAR8 2.40
abcdefg
1.51
a
92.37
def
130.20
bc
333.96
ghi
1.26
efg

ST 10 D VAR9 2.32
abcdefghi
1.48
a
91.65
jk
137.52
a
353.84
fghi
1.88
a

ST 10 D VAR10 2.50
abc
1.47
a
90.47
n
126.54
cd
698.94
b
1.41
cd

HSD 5% 0.62 0.34 0.43 3.87 105.60 0.11

th

Figure 2. Effect of genotypes on chinese flowering cabbages colour.

Figure 2 shows that genotype number 6 had the lowest value of the colour (dark green),
whereas genotype number 3 had the highest colour value (light green).However, the test of LSD at
the level of 5% all types of varieties were not significantly different in colour values. The colour
influenced by the content of chlorophyll is one of the parameters that affect the appearance of the
product. Genotype number 3 had lower chlorophyll content than genotype number 6. Furthermore,
colour values were significantly different for 0, 5 and 10 days-storage. During storage, chinese
flowering cabbage colour changes because the process of respiration continues. Table 3 shows the
genotypes no 3,4, and 5 were not significantly different from control genotypes number 9 and 10 for
the colour values in 5 days-storage.

Figure 3. Effect of genotypes on chinese flowering cabbages moisture.

Chinese flowering cabbage moisture was significantly affected by genotypes. Figure 3
shows genotype number 4 was the highest water content, whereas the lowest levels of water
contained was genotype number 10. Moisture was inversely related to chlorophyll and fiber content
of which is a component of dissolved solids in chinese flowering cabbages. The moisture of
genotype number 5 was not significantly different from control genotype number 7 and 8.
Table 2 also shows that moisture values were significantly different between 5 and 10 days-storage.

Figure 4. Effect of genotypes on chinese flowering cabbages ascorbic acid
th

Figure 4 shows that the ascorbic acid content in genotype number 5 was the highest value.
Ascorbic acid is affected by the type of varieties and seasons (Hanson et al.,2011). Genotypes
number 1,2 and 5 were not significantly different in ascorbic acid contents. Ascorbic acid is one of
the components with high nutritional value in chinese flowering cabbages as other cabbage type
vegetables such as broccoli (Jagdish Singh et al.,2007). During storage ascorbic acid becomes
unstable (Hounsome et al., 2009) as also indicated in Table 2. However, genotypes number 3.5, 6,
and 7 showed the values of ascorbic acid contents were relatively stable for 5 days-storage (Table
3).

Figure 5. Effect of genotypes on chinese flowering cabbages chlorophyll content

Genotype number 10 had the highest chlorophyll content (Figure 5). The chlorophyll
content affected the colour of the leaves that made it become greener. The chlorophyll content of
genotype number 5 was not significantly different from control genotype number 6 and 9. While
genotypes number 1 and 4 were not significantly different from control genotype number 7.
The content of chlorophyll rapidly declines during storage. Storage in the dark room will decrease
the speed of leaf colour change from green to yellow (Zhang et al., 2011, In Press).

Figure 6. Effect of genotypes on chinese flowering cabbages fiber

Fiber content of genotype number 10 had the highest value. Genotype number 5 was not
significantly different from genotype number 10, as well as the interaction 5 days-storage and
genotype varieties were not significantly different for number 5 and 10.

Conclusion

1. Genotypes of chinese flowering cabbage gave effects on moisture, ascorbic acid,
chloropyll, and fiber of chinese flowering cabbages
2. Storage time gave effects on texture, colour, moisture, ascorbic acid, chlorophyll, and fiber
of chinese flowering cabbage.
3. Three genotypes still had good qualits up to 5 days on cold storage.
th
References

Anonymous, 2010. Statistik Indonesia. Biro Pusat Statistik. Jakarta.220-225.
Dris, R., Niscanen, R., and Jain, S. M. 2003. Crop Management and Postharvest Handling of Horticultural
Product Volume II Fruits and Vegetables. Science Publishers, Inc, Enfield NH. USA. Pp 1-22 and 89-
106
Hanson P, Yang, R-Y., Chang, L-C., Ledesma, L. ,and Ledesma, D. 2011. Carotenoids, ascorbic acid, minerals,
and total glucosinolates in Choysum (Brassica rapa cvg. parachinensis) and Kailaan (B. oleraceae
Alboglabra group) as affected by variety and wet and dry season production. Journal of Food
Composition and Analysis. 24(&): 950-962.
Hounsome, N., Hounsome, B., Tomos, D. and Edwards-Jones, G.2009. Changes in antioxidant compounds in
white cabbage during winter storage. Postharvest Biology and Technology 52(20):173-179.
Jagdish Singh, A.K. et al. 2007. Variability of carotenes, vitamin C, E and phenolics in brassica vegetables.
Journal of Food Composition and Analysis. 20 (2): 106-112
Siemonsma,J.S. and Piluek,K(Editors).1994. Plant Resources of South- East Asia 8 Vegetables. Prosea
Foundation . Bogor, Indonesia. Pp.123-126
Zhang, X., Zhang, Z., Li, J., Wu, L., Guo, J., Ouyang, L., Xia, Y., Huang, X., and Pang, X. 2011. Correlation of
leaf senescence and gene expression/activities of chlorophyll degradation enzymes in harvested chinese
flowering cabbage (Brassica rapa var. parachinensis). Journal of Plant Physiology. Article in Press.

th
Influence of Organic Fertilizer on Growth and Vitamin E Content of
Traditional Vegetable, Codonopsis lanceolata

Futoshi Kato
a,*
, Naoto Inoue
a
, Seishi Yoshida
b

a
Faculty of Agriculture, Shinshu University, Nagano, Japan

b
Nagano Prefecture Vegetable and Ornamental Crops Experiment Station, Nagano, Japan
* Corresponding author: Faculty of Agriculture, Shinshu University. 8304 Minamiminowa,
Nagano 399-4598, Japan.
Tel.: +81 265 77 1409 ; fax: +81 265 77 1409.
[email protected]

Abstract

Codonopsis lanceolata (Sieb. et Zucc.) Trautv. is wild vegetable found in East Asian countries and considered
valuable, especially among the Korean people. The effects of organic fertilizer application on the yield and
quality of rhizome were investigated under Andosol condition. Commercial barnyard manure fermented with
crushed bark, beef cattle dung, and leaf mold of Japanese oak were applied at the rates of 0, 5, 10, 15, and 20
gm
-2
. Barnyard manure enhanced the fresh weight of rhizome, but decreased the vitamin E content. The C/N
ratio in the soil surface up to the depth of 30 cm, which was controlled by the application ratio of barnyard
manure and leaf mold, drastically influenced the rhizome yield. Total N, soluble P, exchangeable K, Ca, and Mg,
however, did not significantly affect the rhizome yield. There was significantly negative correlation between the
fresh weight of rhizome and the -tocopherol (vitamin E) content at harvest time. The highest vitamin E content
was observed with the leaf mold application rate of 10 gm
-2
, and the contents achieved at 910 mgDM
-1
. The
nitrogen supply from the soil to plants influenced primarily the yield and quality as vegetable or drug. The vitamin
E content under higher soil C/N ratio was one of the highest among commercial vegetables in the common
Japanese food market.

Keywords: -tocopherol, East Asia, fertilizer application, wild vegetable

Introduction

Food must always be safe and nutritious. Traditional vegetables grown on organic farms
are becoming popular in markets in East Asian countries. The organic cultivation of vegetables has
increased because organic farming benefits human health and is also effective for the conservation
of agricultural environments.
Codonopsis lanceolata (Sieb. et Zucc.) Trautv. is a perennial climbing herb that is a
popular fancy vegetable in high demand among organic foods in Korea. On the other hand, it is
recognized as a rare and quaint wild plant mainly inhabiting mountainous areas in Japan (Figure 1).
C. lanceolata is chemotaxonomically similar to Codonopsis pilosula (Wang et al., 1995), which is a
major source of the traditional Chinese drug dangshen (Iwai et al. 1992; Namba et al., 1992a,
1992b). The natural population of C. lanceolata is distributed throughout shaded and humid sites in
Korea, China, and Japan. Many farmers domesticate, produce, and sell C. lanceolata for its
rhizome vegetable, which is used in a distilled spirit, traditional medicine, or as a foodstuff in Korea.
The Korean common name for this plant is deo-deog. Korean and Chinese people have been
carefully protecting and fostering C. lanceolata as a useful vegetable and drug since ancient times
(Park and Lee 1991; Pemberton and Lee 1996; Sakamoto 1998).
C. lanceolata is also used as a minor vegetable and in a distilled spirit in Central Japan
(Inoue 1998a; 1998b). Furthermore, the native Ainu people use it as a familiar vegetable, drug, and
medicinal plant (Shiraoi Ainu Museum 1989; Annetai et al. 1996; Fukuoka and Sato 1995; Hayashi
1968). The common Japanese name for C. lanceolata is tsuru-ninjin; tsuru means vine and
th
ninjin means rhizome. The Ainu names are chir-muk and tope-muk. Local names in Central
Japan include tou-do, to-dog, and jii-sob.
The cultivation area of C. lanceolata has increased to over 1000 ha in South Korea
because the edible rhizome has a good aromatic flavor (Lee et al. 1996), good texture, and high
antioxidant activity (Maeng and Park 1991). However, the chemical composition of the rhizome
fluctuates according to the cultivation conditions; at present, the optimal soil conditions for
producing high-quality rhizomes are unknown. For providing a high-quality vegetable for healthy
functional foods, productivity testing is important to clarify the effects of organic fertilizer application
rate on the yield and vitamin E content, which is responsible for the antioxidant activity of C.
lanceolata rhizomes.
In this study, field experiments were carried out to investigate the effects of commercial
barnyard manure fermented with crushed bark, beef cattle dung, or leaf mold of Japanese oak on
the rhizome yield and -tocopherol (vitamin E) content in C. lanceolata rhizomes at the end of 1
growing season.

Figure 1. Codonopsis lanceolata (Sieb. et Zucc.) Trautv. (family Campanulaceae).


The experimental field was located at Shinshu University, Minamiminowa Village, Nagano
Prefecture, Japan (alt. 740 m, 35N and 138E). The soil taxonomy and texture are Andosol and
clay loam according to the FAO/UNESCO and international systems, respectively. Commercial
barnyard manure that was fermented with crushed bark (80%), cattle dung (20%), and leaf mold of
Japanese oak was prepared before seeding. Table 1 shows the chemical compositions of the soil
and organic fertilizer. Two organic fertilizers were applied at rates of 0, 5, 10, 15, or 20 gm
-2
and
plowed to a depth of 35 cm below the soil surface just before transplanting the seedlings. The
experimental design was a random block design with 4 replicates. For all treatments, the plot size
was 100 100 cm with 15 cm spacing between individuals. A nylon net was placed to allow the
vines to climb.
Samples from the local population in Young Weoul, Kang Weon Province, South Korea were
prepared, and seedlings with 4 leaves were transplanted into each plot in early May. Rhizomes
were harvested in early November.
Soil samples were collected to a depth of 30 cm before and after fertilization and air-dried at
room temperature. The total carbon and nitrogen contents of the soil were determined using a C-N
corder (Yanaco, MT700). Ammonium-N and NO
3
-N in the soil were extracted with 2 N KCl solution
and measured by Bremners method. Soluble P in the soil was determined by Truogs method.
Exchangeable K, Ca, and Mg were extracted with 1 N acetic ammonium solution and measured by
A: inflorescence and vine; B: capsule and single seed; C: rhizome
The plant sample was collected atu Yong Weoul in Kangwon province of Korea
th
atomic absorption spectrochemical analysis. Total -tocopherol (as vitamin E) content in the
rhizome was measured by high-performance liquid chromatography (HPLC).

Table 1. Chemical properties of soil fertilizer

Constituent Soil
Organic fertilizer
Barnyard manure Leaf mold
pH (H
2
O) 6.3 7.1 6.8
EC (ms) 0.06 2.2 0.5
CEC (me) 22.5 36.7 44.6
Total N 0.5 2.2 0.9
Total C 9.3 23.8 23.8
C/N ratio 17.3 10.9 25.9
Inorganic N (NO
3
) 2.4 11.6 0.2
Inorganic N (NH
4
) 0.7 5.8 1.8
Soluble P 17.7 787.8 58.9
Exchangeable K 41.6 56.6 25.1
Exchangeable Ca 398.4 302.3 239.1
Exchangeable Mg 50 29.2 18.7

Table 2. Correlation between chemical component in soil and rhizome yield

Constituent Correlation coefficient significant
Total N 0.58 P < 0.100
Total C 0.22
Soulble P 0.47
Exchangeable K 0.23
Exchangeable Ca 0.05
Exchangeable Mg 0.04
C/N ratio -0.90 P < 0.001

Results

During the growth period, the precipitation on the site was 600 mm, mean air temperature
ranged from 1024C, and mean solar radiation was approximately 15000 Jcm
-2
day
-1
.
The application ratio of barnyard manure and leaf mold strongly influenced the rhizome
yield at harvest time. The barnyard manure increased the rhizome yield, whereas fermented leaf
mold decreased the yield. The correlation between the soil chemical conditions after fertilization and
rhizome weight at harvest time was analyzed using all of the data (Table 2). There was a significant
negative correlation between C/N ratio and rhizome weight (Figure 2). On the other hand, total N,
total C, soluble P, and exchangeable K, Ca, and Mg in the soil after fertilization did not significantly
affect the rhizome yield. The C/N ratio in the soil from the surface to a depth of 30 cm, which was
controlled by the application ratio of barnyard manure or leaf mold, strongly influenced the rhizome
yield.
Barnyard manure increased the fresh weight of rhizomes but decreased the vitamin E
content (Figure 3). There was a significant negative correlation between the fresh weight and
vitamin E content of rhizomes (p < 0.001). The highest vitamin E content occurred with the
application of 10 gm
-2
leaf mold (910 mgDM
-1
). The nitrogen supply from the soil to plants
primarily influenced the yield and quality of the rhizome as a vegetable or drug. The vitamin E
contents produced under higher soil C/N ratios are one of the highest among commercial
vegetables available in the Japanese food market.
th

Discussion

The natural habitat of C. lanceolata is cool shaded forest floor in mountainous areas in
Korea and Japan. In this experiment, moderate amounts of rhizomes were harvested in only 1
growing season and despite a lack of shade, suggesting that the climate of the experimental field is
favorable for both vegetative growth and rhizome production. Lee et al. (1996) reported that shading
decreases the growth but improves the aromatic constituents. Our results and the previous report
suggest that shading and the fermented organic fertilizers favor production of high-quality
vegetables.
Our survey in South Korea (Sakamoto et al., 1998) revealed that organic farmers in
Kangwon Province have developed an organic fertilizer consisting of saw dust, rice bran, and rice
chaff; it is mixed and fermented over 1 year and applied at a rate of 6 gm
-2
before seeding. The key
technique of the organic manure production is considered to maintain the soil C/N ratio around 17%
in the case of Andosol soils according to our results.
Wang et al. (1995, 1996) report that C. lanceolata is chemotaxonomically similar to C.
pilosula and contains many polysaccharides that exhibit immunomodulatory effects. Maeng and Lee
(1991) also report that the ethanol extract from C. lanceolata rhizome possesses effective
antioxidant activity that is stronger than that of extracts from Panax ginseng C. A. Meyer. In
addition, they point out that C. pilosula rhizome exhibits protective action on experimentally induced
gastric ulcers in rats (Wang et al., 1997). These reports and our present results suggest that the
rhizome of C. lanceolata is a healthy food. Despite the trade-off between rhizome yield and quality,
organic farming with an organic fertilizer that supplies nitrogen slowly is considered valuable in
commercial food production.
C. lanceolata is also a traditional wild vegetable eaten by the Ainu people in Northern
Japan. The screening research of the chemical composition in wild plants used by the Ainu
revealed that the species has the highest vitamin E content among 67 tested species (Annetai et
al., 1996). It is also reported that most edible wild plants have vitamin E contents less than 0.5
mg100 g
-1
fresh weight; on the other hand, vitamin E content of the rhizome of C. lanceolata is 2.38
mg100 g
-1
fresh weight. Our results show that greater amounts of vitamin E are present in smaller
rhizomes produced under higher C/N ratios due to the fermented leaf mold. Since the vitamin E
contents of C. lanceolata are one of the highest among commercial vegetables in the Japanese
food market, the vegetable is expected to be gradually accepted as a worthwhile healthy food.
y = -0.063x + 3.718
(p < 0.001)
2
2.5
3
3.5
0 5 10 15 20 25
-
t
o
c
o
p
h
e
r
o
l

(
m
g

/

1
0
0
g

f
r
e
s
h

m
a
t
t
e
r
-
1
)
Fresh weight of rhizome (g / plant
-1
)
Figure 3. Relationship between rhizome yield and -
tocopherol.
y = -2.42x + 56.4
y = -8.70x + 167.6
0
5
10
15
20
25
14 15 16 17 18 19
F
r
e
s
h

w
e
i
g
h
t

o
f

r
h
i
z
o
m
e

(
g

/

p
l
a
n
t
-
1
)
C/N ratio in soil (0-30 cm)
Barnyard manure
Leaf mold
Figure 2. Relationship between C/N rations soil and
rhizome yield.
th
Many wild species of Campanulaceae are believed to be useful ingredients in drugs that
maintain the human health while being functional foods among Asian peoples. For example, many
species of Platycodon, Campanula, and Adenophora are popular as traditional crude drugs and
foods. Many Korean people and researchers of Korean herbal medicines believe that C. lanceolata
is a functional food that has anti-cancer activity. Hata et al. (1998) point out that many edible wild
plants in Akita prefecture, Japan induce cell differentiation, including the activity of the human
leukemia cell line (HL60), which is a useful model system for drug screening. However, Inoue
(2003) reports that the ethanol-soluble fraction from the rhizome of C. lanceolata does not exhibit
the nitroblue tetrazolium reduction activity for the human promyelocytic leukemia cell line HL60 or
neutrophil activity. In addition, the rhizomes do not inhibit melanine synthesis in mouse melanoma
cell line B16. More investigation is required from other perspectives regarding the anti-cancer
activity of C. lanceolata rhizomes to establish its status as a healthy food.

Acknowledges

We thank emeritus Professor Dr. Sadao Sakamoto of Kyoto University and Professor Dr. Choel-Ho
Park, Kang Weon National University in Korea.

References

Annetai, M. Ogawa, H., Hayashi, T., Aoyagi, M., Chida, M., Muraki, M., Yasuda, C., Yabunaka, T., Akino, S. and
Yano, S. 1996. Studies on wild plants traditionally used by the Ainu people. Part I. Contents of vitamin A,
C and E in edible plants. Report of Hokkaido Eisei Kenkyushyo 46: 34-39.
Fukuoka, I. and Sato, S. 1995. Botanical Memories of Ainu. Sofukan, Tokyo. p.177-180.
Hata, K., Ishikawa K. and Hori, K. 1998. Differentiation - inducing activities of human leukemia cell line (HL60)
by extracts of edible wild plants in Akita. Natural Medicines 52(3): 269-272.
Hayashi, Y. 1968. Foods and life of Ainu people. In Education Board of Hokkaido ed., Ethnological research
note of Ainu. 92-113.
Inoue, N. 1998a. Traditional use of wild plants in Okumibu, Shinshu. Agricultural Technology and Culture 21:
159-191.
Inoue, N. 1998b. Turu-ninjin (Codonopsis lanceolata). In Fujimaki, H. ed., Dictionary of biological resources in
Japan. Noubunkyo, Tokyo. p.215-216.
Inoue, N. 2003. Traditional use and quality as food of edible wild plant Codonopsis lanceolata Trautv. in the
mountainous area of Japan and Korea. The Annals of Environmental Science, Shinshu University 25:
29-44.
Iwai, M., Komatsu, K. and Namba, T. 1992. Pharmacognostical Studies on the Codonopsis plants. (3) On the
botanical origin of Chinese crude drug Danshen derived from sect. Electae plant (I). Shoyakugaky
Zassi 46(3): 217-223.
Lee, S. P., Kim, S. K., Nam, M. S., Choi, B. S. and Lee, S. C. 1996. Effects of shading and organic matter
applications on growth and aromatic constituents of Codonopsis lanceolata. Korean J. Crop Science
41(4):496-504.
Maeng, Y. S. and Park, H. K. 1991. Antioxidant activity of ethanol from Dodok (Codonopsis lanceolata). Korean
J. Food Sci. Technol. 23(3): 311-316.
Namba, T., Komatsu, K., Iwai, M. and Xu, G. F. 1992a. Pharmacognostical Studies on the Codonopsis plants.
(1) On the anatomical characteristics of the root of sect. botanical origin of Chinese crude drug
Danshen derived from sect. Codonopsis plants. Shoyakugaky Zassi 46(2): 156-164.
Namba, T., Komatsu, K. and Iwai, M. 1992b. Pharmacognostical Studies on the Codonopsis plants. (2) On the
botanical origin of Chinese crude drug Danshen and its related crude drugs derived from sect.
Codonopsis. Shoyakugaky Zassi 46(2): 165-173.
Park, C. H. and Lee, K. C. 1991. Production of edible wild plants in Korea. Sun Jin Mum Hwa Sa, Seoul.
Pemberton, R. W. and Lee, N. S. 1996. Wild food plants in South Korea; market presence, new crops, and
exports to the United States. Economic Botany 50(1): 57-70.
th
Sakamoto, S. 1998. Comparative ethnobiological studies in the area surrounding the Japan Sea, especially in
Korea and Japan. Bulletin of the interdicipinary Research Institute of Environmental Sciences 17: 79-95.
Shiraoi Ainu Museum .1989. Chiru-Muck. In Shiraoi Ainu Museum ed., Ainu people and plants. Shiraoi Ainu
Museum, Hokkaido 21.
Wang, Z. T., Ma, G. Y., Tu, P. F., Xu, G. J. and Ng, T. B. 1995. Chemotaxonomic study of Codonopsis (family
Campanulaceae) and its related genera. Biological Systematics and Ecology 23(7/8): 809-812.
Wang, Z. T., Ng, T. B., Yeung, H. W. and Xu, G. J. 1996. Immunomodulatory effect of a polysaccharide-enriched
preparation of Codonopsis pilosula root. Gen. Pharmac. 27(8): 1347-1350.
Wang, Z. T., Du, Q., Xu, G. J., Wang, R. J., Fu, D. Z. and Ng, T. B. 1997. Investigation on the protective action
of Codonopsis pilosula (Dangshen) extract on experimentally-induced gastric ulcer in rats. root. Gen.
Pharmac. 28(3): 469-473.

th
Review on the Effect of Postharvest Treatment on Potato Quality

Ali Asgar

Indonesian Vegetables Research Institute
Jl. Tangkuban Perahu No. 517 Lembang 40791
Tel.(022)2786245, PO BOX 1586 Bandung, Indonesia
[email protected]

Abstract

Research on tuber quality, storage, and processing was carried-out. Research emphasized on the evaluation of
clones for processing quality, on-farm evaluation of promising storage technologies, and application of
techniques to control postharvest losses due to pest and diseases, transportation, storage and marketing to aid
in the management control at pest and disease and in the process upgrade of participating of laboratories,
stores and farmers practices. Research on improving of processing method is needed to increase the quality of
product including flavor. Research on packaging is mainly concentrated on the development of suitable
packaging system for the product.

Keywords: post-harvest treatment, potato, quality, income.

Introduction

Among major vegetables, potato is potential to increase small farmer income, since potato
is economically competitive vegetable. Potatoes are highly demanded by food industries such as
french fries restaurants and potato chips industries. As estimated by World Bank, vegetable and
fruit consumption in Indonesia increased approximately 3.9% during the period of 1995-2010
(Pasandaran & Hadi 1994). Demand projection to overall vegetable increases by 4.1% every year
(8.2 to 12.3 million tons every year, Van Lishout, 1992).
The major challenge for Indonesian agriculture is how to produce high quality of potato at
affordable prices that fit into the demands as rapidly growing population. It was clear that AARD
plays an important role on vegetables quality. Postharvest technology increases product quality and
reduces losses. Loss assessment of poor postharvest technology is estimated about 20 40%
(Winarno & Aman, 1981).
Basic research program has to emphasize on strengthening the vegetable quality by
improving efficiency of farming techniques, utilizing of the valuable domestic resources wisely to
endure food safety, efficiency on management, food security and agribusiness development.
Determination of some pre and postharvest treatment were evaluated for potato quality. Pre-harvest
treatment commonly concerned with variety and harvest time, whereas postharvest concerned with
fresh handling and processing.
In Indonesia, there are a few research on postharvest aspect of potato have been carried
out. Postharvest experiments so far concentrated on the storage and handling of seed and potato
tubers. In this paper we summarized the postharvest treatment affected the quality of potato.

Material and Methods

Several reports provided by IVEGRI were available fragmentally. Reserach started from
potato varieties up to postharvest have been done, however, they need more improvement.
Sequence of postharvest information were hardly found, however, some crop varieties, some
postharvest experiments on various crops and some agronomic aspect methods were described
th
briefly. Field testing design commonly used were randomized block design, whereas in the
laboratory most research were carried-out by complete randomized design with sufficient replication
related to number of treatments. Postharvest treatment methodology related to the some vegetable
varieties testing were mainly based on physical characterization, chemical analysis method and
organoleptic test.
For potato varieties testing, 2-5 g sample was placed in 250 ml flask added with 50 ml of
alcohol 80% and stirred for 1 h, then they were filtered and cleaned. The filtrate of 250 ml contained
carbohydrate. Starch in filtrate as a residue were put on filter paper, and washed 5 times in 10 ml of
ether, then let these samples to evaporate and they were rewashed by 150 ml of alcohol 10% to
obtain free dissolved carbohydrate. Residue was removed and placed in an erlenmeyer flask
through washing by 200 ml of aquadest then added with 20 ml of HCl 25%, covered with cooler lid,
and boiled for 30 min. After that they were cooled down by NaOH 45% and diluted to 500 ml.
Filtered and determined the sugar content as glucose from the filtrate. Determination of starch
content was calculated by glucose weight times factor 0.9. Crop hardness was measured by
penetrometer, and organoleptic test was carried-out by hedonic method.


Storage of seed potatoes
An experiment was conducted to compare the effect of diffuse light and dark storage of
tuber seed on yield of patato by Sihombing (1986). This experiment was carried out at hight land
Ciwidey at West-Java, (1080 m above sea level) on a farmer field in both dry and wet season. A
randomized block design of non-factorial was applied with two storage method having 12 replicates
on each season. The results indicated that the seed tubers stored in diffuse light storage showed
better plant vigour and gave yielded increases from 16.9 to 26.9%, compared with tubers stored in
the dark.
The effect of storage method and delay in planting of tuber seed on yield and quality of
potato tubers was carried-out by Nainggolan (1993). A randomized block design with three
replicates was used in this experiment. Two methods of storage used tuber seed (in dark and
diffuse light) and planting periods (5 months of storage as control). The results showed that storage
of tubers seed in diffuse light storage increased the yield up to 15.02% and the quality of tuber was
better compared to dark storage. The delay in planting of tuber seed decreased the yield to 27.50
g/seed/plant and showed lower quality tuber.
Potato seed storage in mid-elevation area with diffuse light storage was done by Asgar
and Asandhi (1994). The planting time of mid-elevation potato was in May to June, while the tuber
seed used was harvested in December, long storage of potato seed affected poor quality of seed.
One way to overcome the problem was by using diffuse light storage. Six varieties of potato used
diffuse light storage. Six varieties of potato (Granola, Red Pontiac, Cosima, Monza, Cipanas, and
Berolina) were stored in diffuse light storage and dark storage by using randomized completely
block design with six replicates. The results showed that after four months storage the percentage
of rotten tubers of Granola was 69%, although diffuse light storage was better than that in dark
storage in terms of higher number of sprout, shorter, bigger and more healthy.

Storage of ware potatoes
Study on storage of ware potato and the loss due to storage method was conducted by
Asgar and Asandhi (1990). Thirty farmers was sampled for interview. The results showed that some
farmers stored their ware potato for several days until two months when the market price as low
(Asgar, 1990). Two method of storage was used in the field (either covered delaying the harvest or
pilled beside the field and covered with canvas) or in the storage which was usually seed storage.
th
The average loss was 7.1% for farmers having less than 1 ha land and 9.3% for farmers having 1
ha or more land. The highest loss was recorded at 25%.
Improvement of ware potatoes store method was carried-out by Asgar and Asandhi
(1991). A two-layer of box was made in the storage. The distance between the two layers was 14
cm and filled up with rice husk. The box was divided into 12 parts to place the experimental unit
consisted of four treatments and three replicates. The size of the experimental unit was 104 cm
length x 77 cm width x 44 cm depth. The design used was randomized completely block design.
The treatment was pilling potato tubers with: 1) vertical without ventilation, 2) horizontal without
ventilation, 3) vertical with ventilation and 4) horizontal with ventilation. The ventilation made from
proliferated tube was put vertically into the pile. The size of the tube was 74.5 cm of length, 8.5 cm
of diameter, and the number of holes was 20. From this study could be concluded that ware potato
storage using double layers of wall and filled up with rice straw could be introduced to farmers in the
highland, since the temperature in the tubers piles was not significantly different with the room
temperature. However, pilling the tubers horizontally was better than vertically as done by the
farmers.
Experiments on the harvest time and storage period was done by Asgar and Marpaung
(1997). Seed tubers with the size of 25 to 45 g/tuber collected from Pangalengan were planted at
the experimental area at the Indonesian Vegetables Research Institute. The seed tubers were
72/plot. Fertilizing and maintanance at the field was conducted at the Indonesian Vegetables
Research Institute recommendation. Manure was given side of planting with dosage of 30 tons/ha,
ZA at 100 kg/ha, TSP at 250 kg/ha and KCl at 300 kg/ha. Seed tubers were planted with the sprout
of 1 to 2 cm length and planting distance 80 x 30 cm on matches. A split plot design was used and
plants were harvested on day 70, 80, 90, 100, and 110 days. Sub plot was storage period consisted
of 1, 2, 3, 4, and 5 day. The result showed that harvest time of 100 after planting yielded good
quality as evaluated by panelist. The best characteristic was found for tuber harvested on 100 days
after planting and stored for two days.

Processing
The best variety for chips was Atlantic as investigated by Asgar and Kusdibyo (1997) using
method as follows: seed tubers of 2545 g/tuber collected from the farmers in Pangalengan and
Wonosobo were planted at the experimental area of IVEGRI. The seed tubers were 72 per plot.
Fertilizing and maintenance at the field used IVEGRI recommendation (1994). Manure was given
side of planting with dosage of 30 tons/ha. Artificial fertilizer used at planting time were Urea at 200
kg/ha, ZA at 100 kg/ha, TSP at 250 kg/ha, and KCl at 300 kg/ha. Seed tubers were planted with the
sprout of 12 cm in the length and planting distance was 80 x 30 cm on matches. A split plot design
was used in this research and every treatment combination was repeated three times. A main plot
was varieties consisted of Atlantic, Latif, and Granola. A sub-plot was harvest time consisted of 90,
100 and 110 days. The results showed that the quality of Atlantic variety and harvest time of 100
days were the best than the others in terms of the colour, brittleness, taste and appearance.
The chipping quality of 45 advanced potato clones was determined by Asgar and Chujoy
(1999). The results showed that best clones with chipping scores ranged from 1.0 to 3.4 (light
yellow to dark yellow) which were: I-853, ASN-691, Muziranzara, CFJ-691, CEW-691, Atlantic, ABZ-
69-1, TS-2, VC24.16, Cruza-148, LT-5, Monsama, P-4, TS-13, 379706.34, 283232.11, CCN-69-1,
MF-II, CFM-69-1, 3806010.14, 378501.3, Chiqita, Graso-28, I-1150, AGB-69-1, Desiree, I-11035,
Cruza-27, and Precodepa.
Research on the evaluation of 12 potato processing clones was conducted by Basuki et al.
(2003). Experimental area used was at 4 locations i.e: Pangalengan, Garut, Batur (Middle Java),
and Tosari (East Java). Industry for potato chips modern scale, two home industries, and 42
farmers were interviewed to evaluate the production character, tuber quality, specific gravity,
appearance and process product taste from 12 potato processing clones. The results showed that
380584.3 and FBA clones were preferred by farmers, home industry, and consumer. FBA-4 clone
th
coled be developed for modern industry with good handling. TS-2 and MF-II were received by
modern industry processor as raw materials. These clones could be released as new variety for
processing. The product of TS-2 was equal to Atlantic and Panda and product of MF-II was higher
than that of the Atlantic and Panda.
Basuki (2005) showed that according to resistance of the leaf rotting diseases and swollen
root nematodes, 380584.3, TS-2, FBA-4, I-1085 and MF-II clones were resistance. This figure was
achieved from ten experimental areas which were 380584.3 resulted in 33.5 t/ha, TS-2 was 22.4
t/ha, FBA-4 was 28.1 t/ha, I-1085 was 25.3 t/ha and MF-II was 30.1 t/ha, respectively. Furthermore,
he stated that the use of FBA-4, TS-2 and MF-II clones were suitable for raw materials of potatoes
chips for modern industry, while 38058.4.3 and I-1085 were suitable for home industry and middle
class.
Research on distribution of taste on potato slices was conducted by Kastaman et al.
(2000). A completely randomized block design was used in this research. First factor was potato
cultivar consisted of: Atlantic and Granola. Second factor was Sodium Metabisulfite concentration at
500, 750, and 1000 ppm. Third factor was ingridients consisted of: 1) salt, 2) salt and broth, 3) salt
and chicken curry, 4) salt and meat simmered in spices and coconut milk, and 5) salt and pepper.
The results showed that for Atlantic cultivar, dipping with sodium metabisulfite treatment was not
significantly different on the colour, flavor, hardness and taste of potato chips. On Granola, there
was a significantly different on organoleptic characters (colour, taste, appearance). Increasing in
Indonesian spices such as kaldu ayam (chiken broth), kari ayam (chiken curry), rendang (meat
simmersed in spices and coconut milk), and pepper gave significantly different to increase in
consumer preference on organoleptic test. There was an interaction between cultivar and sodium
metabisulfite concentration on the quality. Economic analysis for potato chips on the estimation of
cost price production of Atlantic cultivar was Rp. 15.711/kg. The price of chips was Rp. 16.750/kg,
whereas the price of raw materials was Rp. 4000/kg. For estimation of cost price of Granola cultivar
was Rp. 13.211/kg and a sell price of chips was Rp. 14.240/kg with buying price of raw material at
farmer level Rp. 1500/kg.
Quality assessment for several clones has already done by Asgar et al. (2010). The
objective of this research was to test for clones/cultivars selected from the yield and quality. Quality
test of 10 selective clones was determined. This research was conducted from July to September
2010. The research was arranged in randomized block design. The results showed that chips which
having value between 2.00 and 2.36 (yellow uniform) for potato chips was clone 7 (391011.17 x
385524.9). Reduction sugar content from this clones were assumed to lower than reduction sugar
content of the other potato clones having dark colour.

Conclusions

Considering the increasing demand for processed potato products, a systematic evaluation
of cultivars and clones for processing quality would decrease high research priority. On-farm
evaluation of promising storage technologies for seed and ware potatoes that have already been
tested elsewhere should also be emphasized. Application of technologies to control postharvest
losses due to pest and disease, transit, storage, and marketing were to improve the management
control at pest and disease and in the process upgrade of participating of laboratories, stores and
farmers practices. Research on improving of processing product is needed to increase in the quality
including taste pass through giving spices (flavour). Research on packaging is mainly concentrated
on the development of suitable packaging system for the product.

th
References

Asgar, A. and A.A. Asandhi, 1990. Cara Penyimpanan dan Kehilangan Hasil Kentang Konsumsi di
Pangalengan. Bul. Penel. Hort. XX(1):1-7
Asgar. A. and A.A. Asandhi, 1991. Improvement of Ware Potato Store Method. Bul. Penel. Hort. XX(4):138-142
Asgar, A. and Kusdibyo, 1997. Pengaruh Varietas dan Umur Panen terhadap Kualitas Umbi Kentang (Solanum
tuberosum L.) sebagai Bahan Baku Pembuatan Keripik Kentang. Prosiding Seminar Nasional Teknologi
Pangan. Editor : Slamet Budijanto, Fransisca Zakaria, Ratih Dewanti Haryadi dan Budiatman
Satiawiharja. Perhimpunan Ahli Teknologi Pangan Indonesia. Kantor Menteri Negara Urusan Pangan RI.
Hal:251-262
Asgar, A. and A.A.Asandhi, 1994. Penyimpanan Umbi Bibit Kentang di Dataran Medium dengan Tipe Gudang
Terang. Bul. Penel. Hort. XXVI(2):151-159
Asgar, A. and L. Marpaung, 1997. Pengaruh Umur Panen dan Lama Penyimpanan terhadap Kualitas Umbi
Kentang. J.Hort. 8(3):1208-1216
Asgar, A., S.T. Rahayu, M. Kusmana, and E. Sofiari, 2011. Uji Kualitas dari Beberapa Klon Kentang (Solanum
tuberosum L.) Dataran Tinggi Lembang. In Press.
Basuki, R.S., Kusmana, A. Dimyati, Nur Hartuti, E. Sofiari and U. Jayasinghe, 2003. Evaluation of Processing
Potato Clones in Indonesia. Progress in Potato and Sweet-potato Research in Indonesia. Edited by Keith
O. Fuglie. International Potato Center (CIP) and Indonesian Agency for Agricultural Research and
Development (IAARD).
Basuki. R.S., Kusmana and A. dimyati, 2005. Analisis Daya Hasil, Mutu dan Respons Pengguna terhadap Klon
380584.3, TS-2, FBA-4, I-1085 dan MF-II sebagai Bahan Baku Keripik Kentang. J.hort. 15(3):160-170
Kastaman, R., D.N. Wahyu, Sudaryanto, B.D. Sofiah, C.S. Achyar, A. Asgar and Kusdibyo, 2000. Studi
Pemberian Beberapa Rasa pada Irisan Kentang yang Dikeringkan dengan Metode Penggorengan
Vakum untuk Mendapatkan Mutu Keripik Kentang yang Bernilai Jual Tinggi. Lembaga Penelitian UNPAD
Bekerja Sama dengan Agricultural Research Management Project II. Badan Penelitian dan
Pengembangan Pertanian.
Kusdibyo and L. Marpaung, 1998. Pengaruh Jenis dan Konsentrasi Lilin terhadap ketahan Simpan Kentang
Segar. Laporan Balai Penelitian Tanaman Sayuran.
Nainggolan, P., 1993. Pengaruh Methode Penyimpoanan dan Penundaan Tanam Umbi Bibit terhadap Hasil dan
Mutu Umbi Kentang. Bul. Penel. Hort. XXIV(4):87-92
Pasandaran, E. and P.U. Hadi, 1994. Prospek Komoditi Hortikultura di Indonesia dalam Kerangka
Pembangunan Ekonomi. Penyusunan Prioritas dan Design Penelitian Hortikultura. Solok 17-19
November 1994.
Sihombing, P., 1986. Penyimpanan Umbi Bibit di Ruang Terang terhadap Hasil Kentang. Bul. Penel. Hort.
XIV(2):27-29
Van Lishout, 1992. Consumption of Fresh Vegetables in Indonesia. Internal Comm. No.48. ATA-395 Project.
LEHRI-The Netherlands.
Winarno, F.G. and M. Aman, 1981. Fisiologi Lepas Panen. Sastra Hudaya, Jakarta.

th
Perception, Attitude and Factors Influencing Households Acceptance to
Transgenic Late Blight Resistant Potatoes

Asma Sembiring
*
, Eri Sofiari

Indonesian Vegetable Research Institute, Lembang, Indonesia
*Corresponding author: Indonesian Vegetable Research Institute (BALITSA)
Jl.Tangkuban Perahu No.517 Lembang, Bandung-40395, Indonesia
Tel : +62 22786245; Fax : 62 22786416
[email protected]

Abstract

The objective of this study was to identify the perception, attitude and factors influencing the households
acceptance to the transgenic late blight resistant potatoes. The research used data taken from 101 respondents
in Bandung West Java, Indonesia from September to November 2009 using stratified random sampling. The
surveys showed that most of the respondents (99%) never heard about transgenic potatoes. About 36%
respondents said that transgenic potatoes were safe to be consumed. At least, 55.4% respondents were willing
to consume transgenic potato as long as there was no negative effect by consuming it. In addition, 44.6%
respondents said that they were not willing to consume the potato because they did not know it. Result of Chi-
square test showed that the most factors influencing household acceptance to transgenic potato were
consumption frequency and consumers potato criteria. Statistical analysis using logit binomial test showed that
education and consumers potato criteria were the most important factors for the household to accept the
transgenic late blight resistant potatoes.

Keywords: consumers acceptance, consumers attitude, potato transgenic

Introduction

Potato is the fourth source of carbohydrate in the world and has a big chance as an
alternative food diversification because it contains high nutrient. Potato production centers in
Indonesia commonly locate in high land, with high rainfall and humidity. The condition is very suitable
for late blight (Phytopthora infestans-Mont de Barry disease). Yield loss caused by diseases reached
60 to 80% (Wattimena, 1994). In severe attacked, the loss reached 100%.
The development of resistant potato varieties are one of the solution to reduce yield loss
caused by late blight disease. Several sources of potato resistant to late blight have been found in
some species of wild potatoes such as S. demissum, S. bulbocastanum, S. stoloniferum, and S.
microdontum (Hawkes, 1994). Resistant genes to the late blight from S. bulbocastanum have been
cloned and used to produce potato resistant late blight. The crossing between Katahdin Rb with
Granola and Atlantik resulted in resistant filial to late blight (Song et al., 2003).

In 2004, trial to
Katahdin transgenic potatoes was conducted. The results showed that Katahdin could control late
blight at the early-season. Field trail to examine potatoes resistant characteristic was held in 2007
and 2008 and several filials (F1) resistant to late blight infection.
Kotler

and Susanto (2001)

reported that several factors influence consumer behavior,
including psychology. Psychology aspects involve perception, knowledge, and attitudes become
important aspects in consumer acceptance to the product. Study on consumer behavior to the
transgenic products has been conducted in some countries. The consumer acceptance to the
transgenic products depends on their perception to the benefit and the risk of the transgenic (Byrne,
2006). Supporting of transgenic products come from United State of America and Japan consumers
in agriculture and healthy sectors. The more information consumers get, the more positive response
give to transgenic crops (Hoban, 1999). Other studies showed that respondents knowledge related
th
to transgenic crops and labeling has a negative impact to consumer acceptance (Jill et al., 2001). In
Korea, the consumers tend to reject transgenic food, especially women, people who get high
education and persons who have enough information about transgenic (Onyango et al., 2004).
In Indonesia, the issue about transgenic crops is still in debates. Pros and cons emerge as
the development of transgenic information and the willingness to plant the products with several
reasons. Studies to observe factors influencing household acceptances to transgenic crops has
been done in three big cities in Indonesia, i.e. DKI Jakarta, East Java and North Sumatra concluded
that the less information about transgenic crops consumers have, the easier for consumers to
accept transgenic food. Meanwhile, in economic term, consumers from middle and higher economic
strata are more willing to accept transgenic crops than the consumer from lower economic. Public
acceptance to transgenic crops are also influenced by direct and indirect risk perception from
transgenic food, benefit, risk and the credibility of policy institution in evaluating safety crops and
the environment (Riska, 2009).
Issues on pros and cons about transgenic crops in Indonesia developing bigger than the
product itself. The opponent was greater seen from media coverage rise out the negative effect of
transgenic crops and it will affect consumer acceptances to the transgenic potatoes. In fact, the
product has not been released and sole in Indonesia. The commercialization of transgenic potatoes
shall go through several trial tests in advance such as limited testing of varieties, limited testing
laboratories (bio safety containment) and limited field test (bio safety confainment) based on Bio
safety Commission regulation.
So far, there have been several studies conducted to determine perception, knowledge,
attitude and consumer acceptances to the transgenic cops/foods, yet specifically for Phythopthora
resistant potato varieties. So, the study is expected contribute to increase knowledge related to
consumer acceptances to transgenic crops.


The survey was conducted on September to November in 2009. Household respondents
were chosen as stratification of 101 persons in Bandung municipal, Indonesia. The stratification was
based on income strata. Lower level with income was from IDR 1,000,000 to 2,000,000; middle
level was from IDR 2,000,001 to 3,000,000 and high level was more that IDR 3,000,000.
The variables were characteristic of respondents, perception, attitude and respondent
acceptances to the potatoes transgenic. Data for perception and attitude were counted by
qualitative statements on the ordinal scale (1 to 5) using Likert scale. Whereas, acceptances data
variable were measured by nominal scale (yes or no). Furthermore, the data were analyzed with
Descriptive statistic method, Chi-square test and Logit binomial.


Demographic and Socioeconomic of the Respondents
The sums of respondents were 101, dominated by ages between 31 and 60 years, 78
respondents (78%), with average level of education were senior high school (34%). Most of the
respondents were house wife (67%). Level of income per month were 1-2 millions rupiah (68%).
The potatoes household average consumption renged from 1 to 2 times per week (64%) with
number of consumption was 1,05 kg.

Consumer Perceptions to the Potatoes
Descriptive statistic showed that more than 93% respondents stated that the potatoes was
nutritious vegetable, made healthy, delicious and affordable by consumers, available in the market
th
and easy to be processed for any types of cuisines. As many as 88,1% respondents also said that
the potatoes could be used as staple food (Table 1).

Table 1. Likert scale from household perception to the potatoes

Statements
Percentage (%)
1 2 3 4 5
The potatoes is nutritional food 6,9 91,1 2,0 0,0 0,0
The potatoes is a healthy food 11,9 87,1 0,0 1,0 0,0
The potatoes is delicious food 6,9 89,1 3,0 1,0 0,0
The potatoes price is affordable 6,9 88,1 3,0 2,0 0,0
The potatoes can be used as staple food
The potatoes is available in the market
9,9
31,7
78,2
68,3
1,0
0,0
10,9
0,0
0,0
0,0
The potatoes is easy to be processed 11,9 86,1 1,0 1,0 0,0
(1=strongly agree; 5=strongly not agree, N = 101)

The Consumers Potatoes Criteria
Taste is the most important criteria for the consumers. The results were consistent with
previous study concluded that the consumers noticed more to potatoes tastes (Ameriana et al.,
1998). The color, taste and nutrition were also more important criterias for the potatoes compared
to the price, aroma and the safety to be consumed with value of 72,3; 24 and 50, 5%, respectively
(Table 2).

Table 2. Likert scale from the consumer important criterias to the potatoes


Consumers Perception and Attitude toward Transgenic Potatoes
Table 3 described that 70,3% of respondents always seeked the information of potatoes
consumption. The information included the origin of the potatoes (respondents more likely the
potatoes from Dieng-West Java), safety while be consumed, taste, size and the color.

Table 3. Likert scale on consumers perception and attitude toward the potatoes

. Statements
Percentage (%)
1 2 3 4 5
Always seek information of potatoes consumption.
Knowing transgenic foods on the market
3,0
2,0
67,3
38,6
2,0
12,9
27,7
46,5
0,0
0,0
Knowing transgenic potatoes (raw/processed) on the market. 0,0 0,0 7,9 91,1 1,0
Transgenic potatoes are safe to be consumed 2,0 33,7 20,8 42,6 1,0
Transgenic labeling should be attached 7,9 80,2 3,0 7,9 1,0
Circulation of food made from transgenic potatoes need to be
informed on community
Pros and cons related to transgenic including to potatoes are
occurred because of lack of information on consumer
socialization.
8,9

0,0
78,2

84,2
6,9

10,9
5,9

5,0
0,0

0,0
Transgenic potatoes need to be introduced on the consumers 6,9 90,1 1,0 2,0 0,0

More or less 40,6% of respondents ever heard the circulating transgenic food on the
market. Specifically for the potatoes, most of the consumers (99%) were not informed. Therefore,
Statements Percentage (%)
1 2 3 4 5
Taste 4,0 89,1 2,0 5,0 0,0
Nutritional 9,9 83,2 5,0 2,0 0,0
Appearance 13,9 83,2 1,0 2,0 0,0
Price 5,0 67,3 4,0 23,8 0,0
Color
Aroma
12,9
2,0
83,2
21,8
1,0
4,0
3,0
72,3
0,0
0,0
Safety to be consumed 22,8 26,7 4,0 46,5 0,0
th
definition of potatoes transgenic should have been explained to the respondents at the beginning.
After that, questions related to transgenic were asked. After the explanation, 40 respondents (40%)
said that they would be looking for more information associated with the transgenic potatoes, while
60% of respondents were not decided yet to seek transgenic potatoes information because they
were unaware with the product, beside that, they have already familiar with the potatoes sole on the
market. All consumers were not aware toward transgenic potatoes circulation in the market whether
they were in raw or processed product.
The survey also indicated that fewer consumers (36%) stated that the transgenic potatoes
were safe and edible. Transgenic potatoes were derived by placing a gene from naturally blight
resistant wild potato, so the origin was still from the potatoes, less pesticide and guaranteed from
the government (Curtis et al, 2004) become the reasons of these arguments. Reducing pesticide
becomes essential factor for consumer acceptances to transgenic food (Wen and Rickertsen.,
2002; Hoban, 1999). The positive response from consumers are might because the respondent did
not have enough information about transgenic products (Onyango et al, 2004; Arianti., 2009). Study
conducted by Jill et al (2001) indicated that they had less knowledge about biotechnology, they
though more positive about the use of biotechnology in food production. The rest repondents had
no opinion regarding to the transgenic potatoes since they had no knowledge what transgenic was.
Respondent opinions to the importance of transgenic labeling placed 88%. Consumers
also argued that transgenic potatoes information should be disseminated to the communities.
Furthermore, regarding the potatoes transgenic pros and cons, most of respondents response the
issues emerged because the community awareness toward the issues were still low due to the lack
of information. Therefore, almost all consumers agreed that information about the transgenic
potatoes should be shared to the communities.

Consumer Acceptances toward the Potatoes Transgenic
The consumer acceptances to transgenic potatoes based on the consumer beliefs that the
transgenic potatoes were safe to be eaten, consumer willingness to consume transgenic potatoes
and the influence of debating transgenic potatoes to consumer decision resulted that 55.4% of
consumers were willing to accept transgenic potatoes as long as no negative side effect. Moreover,
the debate about transgenic crops does not affect consumer decisions to eat the product. About
44.6% of respondents were avoid to accept transgenic potatoes because they had no information,
never heard and seen the potatoes, so that they were still reluctant to consume it.
Chi-square to test the connection between two variables among age, education,
occupation, income, consumption frequency, perception, an important potato criterias according to
consumer and attitude showed that only consumption frequency and consumers potato criteria
significant was related to consumer acceptances to transgenic potatoes with value 0,032 and 0,021
(table 4).

Table 4. Chi-Square test (significant in 5%, N=101)

No Statements Chi-square value
1 Age 0.781
2 Education 0.148
3 Occupation 0.687
4 Income 0.549
5 Consumption frequency 0.032*
6 Perception 0.226
7 Criterias 0.021*
8 Attitude 0.303
Significant in 5%.

Meanwhile, logit binomial test indicated that the relationship between variables age,
education, occupation, income, consumption frequency, perception, an important potato criterias
according to consumer and attitude overall to consumer acceptances to transgenic potatoes
resulted that age, occupation, income, consumption frequency and perception did not affect
consumer acceptances to transgenic potatoes. The variables affected consumer acceptances
were education and an important potato criterias with value of 0,028 and 0,013, significant in 5%,
respectively (Table 5).

th
Table 5. Logit binomial test

No Statements Logit value
1 Age 0.515
2 Occupation 0.367
3 Income 0.679
4 Consumption frequency 0.102
5 Perception 0.216
6 Attitude 0.315
7 Education 0.028*
8 Criterias 0.013*
Significant in 5%.

Conclusions

About 55,4% of consumers were willing to eat transgenic potatoes as long as no negative
side effect, while 46% of them were not willing to consume it because they did not have any
information about the products. The most factors influencing household acceptance to transgenic
potato were consumption frequency and consumers potato criteria. Moreover, logit binomial test
showed that education and consumers potato criteria were the most important factors for the
household to accept the transgenic late blight resistant potatoes.

References

Ameriana M, W Adiyoga, L Sulistyowati and D Mamun. 1998. Perilaku konsumen rumah tangga dalam menilai
kualitas kentang. J.Hort.7(4):944-951.
Arianti GD. 2009. Penerimaan petani terhadap produk transgenik. Tesis, Sekolah Pasca sarjana Institut
Pertanian Bogor.
Byrne PF. 2006. Safety and public acceptance of transgenic products. Crop Sci.46 :113-117.
Curtis KR, Jill JMC and TI Wahl. 2004. Consumer acceptance of genetically modified food products in the
developing world. AgBioForum, Vol.7 No 1 & 2, article 13.
Hawkes JG. 1994. Origin of Cultivated Potatoes and Species Relationships in Bradshaw JE, Mackay GR, editor.
Potato Genetics. CAB International. Pp 3-42.
Hoban TJ. 1999. Consumer acceptance of biotechnology in the US and Japan. Food Technology 53(5) 50-53.
Institute of Food Technologies.
Kotler P dan AB Susanto.2001.Manajemen pemasaran Indonesia, Buku 2, Jakarta. Salemba Empat.
Onyango B, R Govindasamy, W Hallman, Ho-Min and VS Puduri. 2004. Consumer acceptance of genetically
modified foods in Korea : factor and cluster analysis. Northeast Agricultural and Resource of Economics
Association and Canadian Agricultural Economics Society Annual Meeting, Canada. June 20-23, 2004.
Riska, 2009. Penerimaan ibu rumah tangga terhadap produk transgenik. Tesis, Sekolah Pasca Sarjana Institut
Pertanian Bogor.
Song J, JM Bradeen, SK Naess, JA Raasch, et al. 2003. Gene RB cloned from Solanum bulbocastanum
Confers Broad Spectrum Resistance to Potato Late Blight. Proc. Natl. Acad. Sci. USA, 100: 9128-9133.
Wen SC and KRickertsen. 2002. Consumer acceptance of GMO: Survey results from Japan, Norway, Taiwan,
and the United States. The Ohio State University Working Paper: AEDE-WP-0026-02.

th
Relations Between the Amyloplast Sedimentation in Tubers and
the Morphogenesis of Tubers in Yams

Michio Kawasaki
a*
, Seito Hosokawa
a
, Hayuru Yoshida
a
,
Kyoko Takahashi
a
, Hiroki Suto
a

a
Faculty of Agriculture and Life Science, Hirosaki University, Aomori, Japan
*Corresponding author: Faculty of Agriculture and Life Science, Hirosaki University,
3 Bunkyo-cho, Hirosaki, Aomori 036-8561, Japan
Tel.: +81 172 39 3815; fax: +81 172 39 3815.
[email protected]

Abstract

Tubers which have different forms in Japanese yam (Jinenjo) and Chinese yams were used in this study. In
developing tubers of all materials, amyloplasts were locally formed at the part beneath the stele in tuber apexes.
However, the numbers of total amyloplasts in each cell and settling amyloplasts in each cell at the parts of
elongating tubers of Nagaimo and Jinenjo were greater than their numbers in the parts of thickening tubers of
Genkotsujirou and Iseimo. When tubers of all materials matured, few amyloplasts were observed at the part. In
this study, we discussed about the relations between the amyloplast sedimentation in tubers and the
morphogenesis of tubers in yams.

Keywords: amyloplast, gravitropism, morphogenesis, starch granule, yam

Introduction

The tuber of Dioscorea is generally regarded as a tuber but it has some characteristics
different from conventional tubers. Therefore the tubers of Dioscorea are also regarded as
rhizophores. The tubers have various shapes. Even in a cultivar or a line, the form of tubers may be
variable. The inconstant nature causes the quality of tubers and the work efficiency to decrease.
Previously we reported that many amyloplasts were locally formed and settled down by gravity at
the apexes of elongating tubers in Chinese yam (Kawasaki et al. 2008). In this study, relations
between the amyloplast sedimentation in tubers and the tuber morphogenesis were investigated by
using some Chinese yam (Dioscorea opposite Thunb.) and Japanese yam (Dioscorea japonica
Thunb.).


Japanese yam (Jinenjo) and Chinese yam, cv. Nagaimo which elongate until their harvest
times to form long tubers, Chinese yam, cv. Iseimo which spherically thickens until harvest time,
Chinese yam, cv. Genkotsujirou which elongates in the initial stage and then spherically thickens,
were used. Developing and mature tubers were sampled and observed with a light microscope.
Morphological characterization related with amyloplasts in tuber apexes was mainly investigated in
this experiment.

th

In developing tubers of all materials, amyloplasts were locally formed at the part beneath
the stele in tuber apexes. However, at the part beneath the stele in tuber apexes, the numbers of
amyloplasts in each cell and amyloplasts which settled down in each cell were not the same among
materials. The numbers of amyloplasts and settling amyloplasts at the parts in elongating tubers of
Nagaimo and Jinenjo were greater than their numbers at the parts in thickening tubers of
Genkotsujirou and Iseimo (Fig.1). In Genkotsujirou, the number of amyloplasts which settled down
at the part of tubers in thickening stage more decreased than it in elongating stage. In tubers of
Iseimo, both the amyloplasts in each cell and the amyloplasts which settled down in each cell at the
part were lower level throughout growing period. When tubers of all materials matured, few
amyloplasts were observed at the part. While amyloplasts had been accumulated in parenchyma of
stele in tubers with growing, their directional bias was not observed in each cell in all materials.
Crystal cells and tannin cells dispersed in the part beneath the stele in tuber apexes as in cortex
surrounding the stele in all materials. The crystals and the tannin bodies were not also ubiquitous in
each cell at the part in each material (Fig.1).
It was shown that the amyloplast sedimentation in tuber apexes was common structural
characteristic in some Dioscorea materials. In root caps of plants, amyloplasts have been reported
to act as gravisusceptors (Blancaflor et al., 1998; Perbal, 1999) and it is known that they are related
to morphogenesis of the roots. The results from this study indicated that the amyloplast
sedimentation would be concerned in gravity perception and the characteristic of the sedimentation
possibly was concerned in the morphogenesis of tuber in each material. We are also carrying out
further research with a lot more cultivars and lines in Dioscorea by using electron microscopes.

(a) Diagram of longitudinal section of tubers. (b) Longitudinal sections of the part beneath the stele in tips of developing tubers.
The sections were stained with toluidine blue O. Arrowheads indicate amyloplasts. Cc, crystal cell; G, the direction of gravity; Tc,
tannin cell. Genkotsujirou was investigated at thickening stage.

Figure 1. Amyloplast distribution in tips of developing tubers.

th
References

Blancaflor EB, JM Fasano and S Gilroy. 1998. Mapping the functional roles of cap cells in the response of
Arabidopsis primary roots to gravity. Plant Physiol. 116: 213-222.
Kawasaki M, M Taniguchi and H Miyake. 2008. Dynamics of amyloplast sedimentation in growing yam tubers
and its possible role in graviperception. Plant Prod. Sci. 11: 393-397.
Perbal G. 1999. Gravisensing in roots. Adv. Space Res. 24: 723-729.

th
Optimalising Potato Productivity in Sembalun Highlands,
Nusa Tenggara Barat Indonesia

Baiq Nurul Hidayah
a*
, Sudjudi
a
, Lia Hadiawati
a
, Dwi Praptomo Sudjatmiko
a
,
Peter Dawson
b
, Terry Hill
b
, Julie M. Warren
b

a
Institute for Assessment of Agricultural Technology, Nusa Tenggara Barat Province, Indonesia
b
Department of Agriculture and Food, Western Australia
*
Corresponding author: Balai Pengkajian Teknologi Pertanian (BPTP) Nusa Tenggara Barat,
Jalan Raya Peninjauan Narmada, Lombok Barat NTB, Indonesia 83010
[email protected]

Abstract

Potato cultivation in Nusa Tenggara Barat (NTB) Province of Indonesia locates in the Rinjani Valley highlands at
1,050 1,250 m above sea level. Farmers grow the Atlantic variety for a crisp processing company. The yield of
Atlantic is low which is about 18.2 ton/ha, however, this is a profitable crop for farmers. Elsewhere in Indonesia
the frequent cropping of potatoes has led to soil quality decline. To reduce the decline, potato farmers in NTB
used compost and superphosphate to increase potato productivity. They also applied a new management
technique. This is important because potatoes are a new crop in NTB and specific management suited to local
conditions which has not yet been developed. The research was conducted at six farmers fields and involving
six Farmer Field School (FFS) groups. The compost treatments applied were local compost at 3,000 and 5,000
kg/ha. The super phosphate treatments applied were 300 and 600 kg/ha. Each treatment had six replicates by
having six different farmer groups which had the same experimental design in their fields. The results showed
that there was no significant difference in yields of super phosphate at 300 and 600 kg/ha which were 33.0 and
33.1 t/ha, respectively. Similarly there was not a significant difference in yield between the compost treatments
with 3,000 kg/ha producing 33.0 t/ha, meanwhile with 5,000 kg/ha of compost produced 32.7 t/ha.

Keywords: productivity, potato, compost, farmer initiated learning, Nusa Tenggara Barat

Introduction

Potato (Solanum tuberosum) is an important vegetable commodity in Indonesia
having a good market, both as a vegetable and raw material for food processing industries.
Because of the high demands, potatoes are expected in the future for diversification of
carbohydrate sources that may increase sustainability and overcome poverity in Indonesia. In
Indonesia, potatoes are produced in 21 provinces, the biggest are in Sumatra and Java with the
cropping area are around 64,148 ha. Demand for table and processing potatoes increases every
year. The value of imported processing potatoes to Indonesia in 2007 was US$ 40 million whch was
about 43,477 tonnes. In 2008 (from January to September) processing potato imports reached
29,187 tonnes with value of US$ 28 million. In 2009 Indonesia imported 48,000 tonnes with value of
US$ 33 million. Indonesian domestic potato production has increased steadily at over 3% per
annum since 1997 and reached 1,176,304 tonnes in 2009 (Badan Pusat Statistik, 2011).
Potato production is generally conventional and traditional or continuing from previous
generations, so that yields are still low which is from 14.9 to16.4 tonnes/ha (average yield in
Indonesia). Many problems are found to increase potato production in Indonesia including: (1) low
quality and quantity of seed potatoes, which forms the main concern in the effort to increase potato
production in Indonesia (Fuglie et al. 2006), (2) current conventional cultivation techniques
(Kuntjoro, 2000), (3) topographic factors, where high areas with suitable temperatures for growing
th
potatoes are very limited (Kuntjoro, 2000), (4) the tropical conditions are optimum for the
development of pests and disease of potato crops (Kuntjoro, 2000).
In NTB, potatoes are mainly cultivated in the Sembalun sub-district on the slopes of Mount
Rinjani, from about 1,050 to 1,250 m asl. Potatoes are now the most important horticultural
commodity for the Sembalun community. The potato variety grown by Sembalun farmers is Atlantic
with a yield of 18.2 tonnes/ha (BPTP NTB, 2009) which is still relatively low because in several
potato studies in Indonesia the yield has been 35 tonnes/ha (BPTP NTB, 2009). Sembalun farmers
can grow potatoes in the dry season as well as the wet season. In the wet season potatoes are
planted in dryland that has a potential area of more than 1,500 ha and in the dry season potatoes
are planted in paddy fields after the rice harvest in the months of June and July with a potential area
of 1,105 ha. In 2010, the percentage of the paddy area used to produced potatoes was just 15 %.
The main constraint to development of Atlantic potatoes in Sembalun is sub-optimal
application of integrated crop management (ICM). Farmers still predominantly use chemical fertiliser
and do not use organic fertiliser although there is the potential to produce and develop the local
organic fertiliser. Farmers are also accustomed to control pests and diseases with chemical
pesticides without observing threshold levels indicating whether control is required or not, also apply
mixtures of various pesticides together without paying attention to the active ingredients causing an
impact on the important natural predators. The dominant use of chemical fertiliser and pesticides is
the reason why potato enterprises have high costs. In fact the constant use of chemical fertiliser will
damage the soil structure and make the soil hard (Nurmayulis and Maryati, 2008). Furthermore, the
excessive use of chemical pesticides will destroy the insect biodiversity and lead to the death of
insects and other microorganisms antagonistic to pests and pathogens (Nurmayulis and Maryati,
2008).
The constant practising of conventional potato production systems will reduce the
profitability of farmers (BPTP NTB, 2009), and in the long term will cause environmental damage
and the loss of biodiversity in this region (BPTP NTB, 2009). Because of this, a sustainable and
environmentally friendly plan to support agricultural development through the study of optimalising
potato yield in the Sembalun highlands is needed. Sembalun is a small, isolated potato production
area without specialist potato support services and so research into optimising potato production
inputs will have to be carried out by the farmers themselves with local extension workers.
To overcome the contraint of sub-optimal crop management a technique was required that
enabled farmers to become their own researchers. The technique used was a modification to the
FFS methodology. The aim was to instigate demonstration plots that allowed the impact of single
management changes to be measured by farmers. Previously the potato FFSs had compared an
ICM plot versus a conventional plot. This resulted in a range of management changes between the
plots which made it difficult to identify the cause of improvements in profits between the treatments.
We call this improved methodology Farmer Initiated Learning (FIL).
This research aimed to help farmers develop and put into use a less costly potato
production system that will significantly increase the ability of small farmers to take up potato
production in the Sembalun highland.


Experimental set-up
Simple FIL experiments to test one variable were introduced to Sembalun Farmer Field
Schools in 2009. The research was conducted at six farmers fields involving six Farmer Initiated
Learning groups. At Sembalun six farmer groups compared the use of superphosphate with
compost. The plots were around 1000 m
2
and all had a 50 m
2
yield assessment sub-plot pegged in
the center. This meant that the yield measured by each farmer group came from the same size plot.
The results from each farmer group were used as replicates. Results were presented on a t/ha
th
basis. The experiment was located at the Sembalun highland of NTB. The FIL groups were all
members of the overarching farmer group Kelompok Horsela. The experiment was conducted at
one growing season from June to November 2009.

Cultural practices and conditions
The compost treatments applied were local compost at 3,000 and 5,000 kg/ha. The
superphosphate treatments applied were 300 kg/ha and 600 kg/ha. Other fertilisers applied were
the same and included; NPK 600 kg/ha and sulphate of ammonia 300 kg/ha. The plot design is
shown in Figure 1.

Farmers conventional
practice
e.g. 600 kg/ha super
phosphate

b
o
r
d
e
R

0.5 m

FIL treatment, 300
kg/ha super phosphate

To the left the farmers usual rate of superphosphate was applied. To the right a lower experimental rate of superphosphate was
applied. Plots varied in size according to individual. Yield was determined by harvesting a 50 m
2
sub-plot in the centre of each
treatment.

Figure 1. Example of experimental plot design.

The simple experiments were executed to plan by the six farmer groups. Yields were
measured and recorded from the yield sub-plots. The results from each of the six farmer groups
were used as replicates in an ANOVA. All the data were statistically analysed using analysis of
variance (ANOVA). The significance of treatment effect was determined using F-test, and to
determine the significance of the difference between the means of the two treatments, least
significant differences (LSD) were estimated at the 5% probability level.


There was no significant difference in yields from superphosphate applied at 300 and 600
kg/ha. The respective yields were 33.0 and 33.1 t/ha (Table 1). Similarly there wasnt a significant
difference in yield between the compost treeatments with 3,000 kg/ha producing 33.0 t/ha while
5,000 kg/ha produced 32.7 t/ha (Table 1). This indicated that farmers can improve their efficiency of
phosphate and compost, therefore, it also meant to improve income through the reduction in the
input costs.
Super phosphate cost was 2000 Rp/kg (BPTP NTB 2009) and the average farmer uses
was 433 kg/ha. The finding that 300 kg of super phosphate is sufficient for potato production in the
paddy areas of Sembalun means that they can save 133 kg of super phosphate or 266,000 Rp/ha
which will improve farmers income through reduced input costs.
Compost at 5,000 or 3,000 kg/ha did not significantly affect the yield of potatoes. Manure
costs 497 Rp/kg (BPTP NTB 2009) and the average farmer uses 3,192 kg/ha. The finding that
3,000 kg of compost is sufficient for potato production in the paddy areas of Sembalun means that
there can be a saving of 192 kg of compost or 95,425 Rp/ha for the average farmer which will also
improve farmer income because of reduced input costs. Farmers who use above average organic
th
manure, the savings will be greater. For example, farmer who previously used 5,000 kg/ha of
compost then he reduced to 3,000 kg/ha, the savings would be 994,000 Rp/ha.

Table 1. Results of Farmer Initiated learning-by-doing plots investigating the effect of lower super phosphate
and compost rates NTB 2009

Treatment Description
Yield
(t/ha)
Super phosphate
300 kg/ha experimental rate 33.0
600 kg/ha farmers usual application rate 33.1
Significance ns
LSD 1.4
n 6.0
Compost
3,000 kg/ha experimental rate 33.0
5,000 kg/ha farmers usual application rate 32.7
Significance ns
LSD 2.8
n 6.0

Conclusions

There was no significant difference in yields resulted from superphosphate at 300 and 600
kg/ha which produced 33.0 and 33.1 t/ha respectively. Similarly there wasnt a significant difference
in yield between the compost treatments at 3,000 kg/ha producing 33.0 t/ha while at 5,000 kg/ha
produced 32.7 t/ha. Therefore farmers can improve their efficiency of phosphate and compost
inputs to improve income through reduced input costs. The six FIL groups within Kelompok Horsela
demonstrated that these farmers and their agricultural extension workers now have the capacity to
plan and coordinate a series of simple though specialized potato experiments. Sub-group results
could be analyzed as replicates in an ANOVA of the combined results. This means that this isolated
group of farmers can now undertake their own objective testing of new management techniques.

Acknowledgments

We would like to thank the Australian Centre for International Agricultural Research (ACIAR), Balai
Pengkajian Teknologi Pertanian (BPTP) Nusa Tenggara Barat Province and the Department of Agriculture and
Food, Western Australia (DAFWA) for funding this project. The assistance of collaborator farmers from
Kelompok Horsela and extension workers from Dinas Pertanian, Kecamatan Sembalun, is gratefully
acknowledged too.

References

Badan Pusat Statistik, 2011. Produksi Sayuran di Indonesia. Accessed 9 March 2011.
http://www.bps.go.id/tab_sub/view.php?tabel=1&daftar=1&id_subyek=55&notab=15.
BPTP NTB, 2009. Sosial Ekonomi Kentang Sembalun. (Balai Pengkajian Teknologi Pertanian NTB, Narmada)
English translation attached to ACIAR Final Report AGB/2005/167 Appendix 2 Economic Baseline Survey
of Potatoes. http://aciar.gov.au/publication/FR2011-24
Fuglie, KO, W Adiyoga, R Asmunati, S Mahalaya and R Suherman. 2006. Farm demand for quality potato seed
in Indonesia. Agricultural Economics 35: 257-266
Kuntjoro, A.S., 2000. Produksi Umbi Mini Kentang G0 Bebas Virus melalui Perbanyakan Planlet secara Kultur
Jaringan di PT. Intidaya Agrolestari (Inagro) Bogor Jawa Barat. Skripsi. Jurusan Budidaya Pertanian
Fakultas Pertanian, Institut Pertanian Bogor. Pp 62.
th
Nurmayulis and Maryati, 2008. Content of Nitrogen and Yield of Potato Supplied with Fermented Organic Matter,
Azospirillum sp., and Nitrogen Fertilizer in Cisarua, Lembang, West Java. Jurnal Tanah Trop., Vol 13, No.
3, Pp 217-224

th
Transformation and Transient Ekspresion Analysis of L-HBsAg DNA in
Fruits of Musa acuminata Colla cultivar Ambon Lumut and Mas using
Agrobacterium tumefaciens

Sony Suhandono*, Lailatul B, Ernawati Giri R, Putri DU, Dina RR, Ima MZ

School of Life and Sciences, Bandung Institute of Technology, Bandung, Indonesia
* Corresponding author: Bandung Institute of Technology. Jl. Ganesa No 10, Bandung 40132,
West Java, Indonesia.
Tel./fax.:+62-22-2534107, +62-22-2511575.
[email protected]

Abstract

Conventional HBsAg is still expensive for most Indonesia citizens. Recently, scientists developed plant-based
vaccine which will give easy delivery, flexible production scale up, and produce cheaper vaccine. Agrobacterium
transformation has been widely used in genetic engineering. This research was conducted to transform and
analyze the L-HBsAg DNA expression in banana fruit using Agrobacterium tumefaciens and vacuum infiltration
method. Unripe Musa acuminata Colla cultivars Ambon Lumut (AAA) and Mas (AA) were used in this
transformation. The slices of banana were co-cultivated with A. tumefaciens strain AGL1 for Ambon lumut and
GV3101 for Mas banana in three days at 25C1C in the dark. Both strains contain a plasmid pCAMBIA 1390
with MeEF-1 promotor and L-HBsAg gene. Expression of L-HBsAg was confirmed by using RT-PCR with gene-
specific primers of L-HBsAg. A 1,323 bp band of L-HBsAg was observed in gel electrophoresis as a result of RT-
PCR. The sequence of recombinant plasmid was read with specific primers for L-HBsAg. These steps were
performed using MACROGEN services. These results indicated that the cDNA sequences of samples and
protein-coding DNA sequences of L-HBsAg were identical. Therefore, it can be concluded that the L-HBsAg
DNA was inserted and expressed in unripe fruits of Ambon lumut and Mas banana.

Keywords : transformation, Agrobacterium tumefaciens, L-HBsAg gene, Musa acuminata, ambon lumut banana,
mas banana

Introduction

Hepatitis B is infectious disease caused by Hepatitis B virus (HBV). It was estimated that
more than 400 million people worldwide suffer from this disease (Piramanayagam et al., 2008).
Effort to tackle this problem like vaccination has been available since 1980 (European Centre for
Disease Prevention and Control, 2008). However, the vaccination program does not run well in
developing countries like Indonesia because of the high price of the vaccine and syringe and
inadequate facility for the storage and distribution of vaccines (Streatfield and Howard, 2003). One
of the solutions developed to overcome these problems is the production of vaccine in a plant.
Research on the production of Hepatitis B vaccine in a plant is constantly being developed.
Large hepatitis B surface antigen or L-HBsAg is the latest variant of HBV vaccine. It consists of pre-
S2, pre-S1, and S antigen (Lou et al., 2007). It is expected that vaccination using the L-HBsAg may
trigger immune responses effectively in preventing HBV infection.
Agrobacterium-mediated transformation is a method to be used to transform plant with
foreign DNA fragments encoding L-HBsAg into the plant genome. A segment of Agrobacterium
tumefacines Ti-plasmid called T-DNA is moved from a bacterium cell into the host plant
chromosomal genome. The T-DNA region is bordered by two 25 bp direct repeat sequences, called
left border and right border. After entering the plant host cells, the T-DNA sequence will express
genes that incorporated into it. For this reason, the targeted recombinant gene usually is inserted in
the T-DNA region (Taiz and Zeiger, 2002).
th
One of the plants that can be used to express the hepatitis B vaccine is banana. Banana
trees can be grown in tropical regions and many people from various backgrounds and ages
consumed the fruit. Bananas can be directly consumed so that the degradation process of the
vaccine (protein) due to heating can be avoided (Radji, 2004). In this study expression analysis of
the gene encoding L-HBsAg proteins in Ambon lumut and Mas banana fruit was made transiently
because it requires less time and the result in transgene expression levels could be higher than
stable expression in transgenic plant (Sheludko, 2008).


Plant material
Unripe banana used in this experiment was Ambon lumut and Mas fruits. The banana was
specially ordered from a farmer. Age of the fruit was about three months from flower formation. The
fruit skin color is green and gummy when peeled. While the fruit flesh is white and hard. The fruit
was cut with a thickness of about 2-3 cm. Then the skin of the fruit was peeled off. The pieces were
immersed in 1% sodium hypochloride for 10 min. After that, it was rinsed twice using sterile distilled
water. The soaked pieces were cut again with a thickness of 2 mm. Each of the banana slices as
thick as 2 mm was further divided into 8 sections.

Agrobacterium tumefaciens
Strain A. tumefaciens that used in transformation were AGL1 for Ambon lumut and
GV3101 for Mas banana. Both strains contain a plasmid pCAMBIA 1390 with MeEF-1 promotor
and L-HBsAg gene. The Agrobacterium strain with no binary plasmid was used as a control for the
experiment.
Bacteria were activated on solid YEP medium with antibiotic for three days at 25C1C,
250 rpm, in dark condition. Antibiotics for strain GV3101 were rifampicin at 50 ppm and kanamycin
at 50 ppm. Antibiotics for AGL1 were carbenicilin at 100 ppm, rifampicin at 50 ppm and kanamycin
at 50 ppm. While the bacteria lacking-plasmids were inoculated into the same medium, but without
kanamycin.

Transferred of L-HBsAg gene into banana fruit
The vacuum infiltration method used in this experiment was modified from Matsumoto et al
(2009). Single colony of bacteria was inoculated into 10 ml of liquid YEP medium containing
antibiotics until the cell density has reached an OD
600
of 0.5. An aliquot of 10% of the
Agrobacterium cell suspension was again subcultured in 20 ml of same medium at same condition
until the OD
600
of 0.8. After that, the cells were collected by centrifugation at 2000 g for 5 min and
suspended in infiltration medium on MS (Murashige and Skoog) containing 2% of sucrose, 200
M of acetosyringone, and 0.01% of Silwet L-408.
The banana slices cut and divided into eigth pieces, were put into 1.5 ml microtube
containing 1 ml of the Agrobacterium cell suspension (OD
600
= 0.8) in the infiltration medium. Then
those were subjected to vacuum for 10 min, followed by co-cultivation for three days at 25C1C in
dark condition.

Expression analysis of L-HBsAg gene in banana fruit
To analyze the gene expression of L-HBsAg, the RNA isolation was performed using the
method from Kansas et al (2008). The presence of RNA was confirmed by the protocol on agarose
gel electrophoresis of RNA concentration of 2% (w/v) containing EtBr in 1x TAE buffer. DNase was
added to the RNA preparation to eliminate genomic DNA isolation. Then the reverse transcriptase-
PCR (RT-PCR) was made to convert total RNA into spesific cDNA of L-HBsAg gene in the banana
fruit.
th
The iScript cDNA Synthesis Kit from Bio Rad Laboratories, Inc. were used to reverse
transcript RNA into cDNA. PCR using specific primers of MeEF-1 promotor in 25 cycles was done
to ensure the absence of genomic DNA from the total RNA. PCR was performed with Applied
Biosystem 2720 Thermal Cycler. Primer sequences used were Me-EF1 forward (5
AAGCTTCCAGTGAATGGTCA 3) and Me-EF1 reverse (5TGTGAACCTTCTCTCTAGACATTGTTAGT 3).
The PCR cycles consisted of 5 min at 94
o
C, 30 sec at 94
o
C, 30 sec at 50
o
C, 1 min at 72
o
C, and 7
min at 72
o
C.
An order to amplify the expression of L-HBsAg from cDNA , the primers LHB-forward
(5GGATCCTGATGAAAATGAAGGTCCTTGTTTTCTTCGTTGCTACAATTTTGGTAGCATGGCAATGCCATGC
GATGGGAGGTTGGTCCTCAAAACC-3) and LHB-reverse (5GGTCACCTTAAATGTATACCCAAAGAC-3)
were used. The series of cycles used were five min at 94
o
C, 30 sec at 94
o
C, 45 sec at 55
o
C, 1 min
and 30 sec at 72
o
C, and 7 min at 72
o
C.The PCR reaction composition were dNTP mix at 0,2 mM,
Taq buffer 1x, MgCl
2
1,5 mM
,
of primer forward at 1 M, primer reverse at 1 M, sample cDNA at 1
g, DNA polymerase at 1 unit, and deion.
cDNA from the RT-PCR was cloned using the vector pGEM -T Easy vector system from
Promega. Restriction analysis with EcoRI was made to confirm the clone in the plasmid. Restriction
results were visualized on agarose gel electrophoresis. A nitrogen base sequence of cDNA was
read as the last stage using specific forward and reverse primer L-HBsAg from MACROGEN.


Transformation of L-HBsAg gene into banana fruit
RNA isolation results indicated the presence of two RNA bands that dominant in the mid-
agarose gel, which was ribosomal RNA (rRNA) 28S and 18S (Figure 1a). Quantification of total
RNA with a spectrophotometer showed that the ratio A260/ A280 in samples isolated RNA was
1.36 for Ambon lumut and 1.35 for Mas banana. The ratio obtained indicated that the purity of the
isolated RNA was low because there may contain the impurities, such as genomic DNA and
proteins. Electrophoresis results were also seen on the tape at the top indicating the presence of
genomic DNA. Therefore, the isolation of total RNA were added DNase to eliminate genomic DNA
so it was not interfere the next process.

a. b.

Figure 1. (a) Electrophoresis result of mRNA and (b) RT-PCR product from Ambon lumut (a) and Mas (b)
banana

Confirmation the presence of L-HBsAg gene was made using PCR spesific primer of L-
HBsAg. Electrophoresis results of RT-PCR products is shown in Figure 1b obtained after three
consecutive PCR. This suggests that the gene encoding L-HBsAg was successfully inserted and
expressed in unripe Ambon lumut and Mas banana.
th
Confirmation the presence of L-HBsAg gene was also made by restriction analysis and
reading the sequence of nucleotide bases from cloned RT-PCR result. The results of restriction
(Figure 2b) indicate that the presence of two bands of DNA size at 1300 and 3000 bp in Ambon
lumut and Mas banana.
Final stages was reading the sequence of recombinant plasmid with specific primers for L-
HBsAg. These steps were performed using MACROGEN services. The results from MACROGEN
shows that the cDNA sequences of samples and protein-coding DNA sequences of L-HBsAg are
identical. Therefore, it can be concluded that the cDNA sample was a cDNA of L-HBsAg. This
means the L-HBsAg transgene successfully expressed at the mRNA level (transcription) in unripe
ambon lumut and mas banana in transient system.

Figure 2. (a) restriction map of clone vector, (b) electrophoresis result from white colony that restricted using
EcoRI. Sample 1 was ambon lumut while sample 2 was mas banana

Acknowledgements

Our sincere thanks to PT Mata Pelangi and Mommentive for The Silwet L-408 and Silwet L-77
donation.

References

European Centre for Disease Prevention and Control. 2008. Ann. Epidemiological Report on Communicable
Diseases in Europe. Pages 37, 7685, 146150.
Lou X, Yao Q, Zhang Z, Peng R, Xiong A and Wang H. 2007. Expression of the Human Hepatitis B Virus Large
Surface Antigen Gene in Transgenic Tomato Plants. Clinic. and Vacc. Immun. 14 (4): 464 469.
Matsumoto K, Cabral GB, Teixeira JB and Monte DC. 2009. Agrobacterium-mediated Transient Expression
System in Banana Immature Fruits. African J. of Biotech. 8 (17), pp. 4039-4042.
Piramanayagam P, Choudhuri G and Singh SP. 2008. Hepatitis B: News from the research world. Hep. B.
Annual. 5:146-62.
Radji M. 2004. Pemberian Vaksin Melalui Tanaman Transgenik. Majalah Ilmu Kefarmasian 1 (1).
Sheludko YV. 2008. Agrobacterium-Mediated Transient Expression as an Approach to Production of
Recombinant Proteins in Plants. Recent Patents on Biotech. 2: 198-208.
Streatfield S J and Howard J A. 2003. Plant-Based Vaccines. Intern. J. for Parasit. 33:479-493.
Taiz L and Zeiger E. 2002. Plant Physiology, 3nd Edition. Massachusets : Sinauer Association, Inc.

a
b
th
The Study and Early Evaluation of Resistance of Banana Accessions for
Wilt Disease Caused by Fusarium oxyporum f.sp.
cubense VCG 01213/16 (TR4)

Agus Sutanto
a,b,*
, Sudarsono
a
, Dewi Sukma
a
, Catur Hermanto
b

a
Department of Agronomy and Horticulture, Bogor Agricultural Institute, Bogor, Indonesia
b
Indonesian Tropical Fruit Research Institute, Solok, Indonesia
*Corresponding author: Indonesian Tropical Fruit Research Institute,
Jl. Raya Solok-Aripan Km. 8, PO. Box 5 Solok, West Sumatera Indonesia,
Tel: +62 755 20137, Fax: +62 755 20592
[email protected]

Abstract

Fusarium wilt is one of main diseases of banana in Indonesia. This disease has destroyed banana plantation in
almost all parts of Indonesia and it is difficult to be managed by agronomic and chemical controls. However,
some species/cultivars show tolerance or resistance to Fusarium wilt. It indicates that those species/cultivars
have resistance genes in their genomic DNA. The evaluation of banana plants for Fusarium wilt resistance can
be carried out artificially using young plants from tissue culture. The objectives of this research were to evaluate
young acclimatized tissue culture plants for Fusarium wilt resistance and to study the resistance mechanism of
plant to Fusarium wilt disease. The experiment used five banana accessions; there were Calcuta-4 (AAw),
Ketan (AAB), Klutuk (BB), Kepok (ABB) and Ambon Hijau (AAA), and double compartment for planting system.
Before planting on the plastic cup containing sterile sand medium, roots of the plantlets were dipped in 10
6

conidia suspension of Fusarium oxysporum f.sp. cubense for five minutes. All of the cups containing inoculated
plants were put on the plastic trays. The data were collected five weeks after planting. Base on the value of DSI
(disease severity index) of RDI (rhizome discoloration index) and LSI (leaf symptom index), accessions will be
categorized into highly susceptible, susceptible, tolerant and resistant. Result showed that Klutuk, Calcuta-4,
Ketan and Kepok were categorized as tolerant, while Ambon Hijau was susceptible. All of tolerant accessions
had symptom on leaves (LSI) and/or rhizome (RDI) at low level, and they still grew well.

Keywords: banana, resistance, fusarium wilt, early evaluation

Introduction

Banana is the most important fruit in Indonesia. Based on Ministry of Agriculture database
(http://aplikasi.deptan.go.id/bdsp/hasil_kom.asp) banana contributed 31.10% of national fruit
production in 2009, with the production reached 6.37 million ton. This potecy can support three
main programmes of agricultural development; food security, development of agribussiness and
prosperity. However, the successfull of those programmes are constrained by pests and diseases
development that affect banana plantation with vary disease intensity rank from 0.08-100%
(Hermanto et al., 2011). One of destructive banana diseases in Indonesia is fusarium wilt disease
caused by Fusarium oxysporum f.sp. cubense (Foc). Fusarium wilt control using practical cultures such as
chemical, soil treatments, crop rotation, organic amendments may reduce the severity of the disease but
relatively difficult to be adopted commercially (Pegg et al.,1993), therefore, the use of resistance cultivars is
the best alternative for controlling this disease.
Field evaluation is the most reliable menthod for disease resistance selection, however, it requires
high cost, manpower, space and facing the risk of environmental stress. Afforts to simplyfy the evaluation
procedures have been carried out such as the use of young plant or in vitro calus as selected materials
(Chand et al., 2008), specific pathogen race or toxin as selective agent (Hadrami et al., 2005), and screen
house or in vitro condition as selection method (Vbov and Lebeda, 2005). The objectives of this
th
research were to evaluate young acclimatized tissue culture plants for fusarium wilt resistance and
to study the resistance mechanism of plant to fusarium wilt disease


Planting Material, Foc Inoculation and Planting
The experiment used 10-15 cm in size of acclimatized in vitro plantlets of five banana
accessions; Calcuta 4 (AAw), Ambon Hijau (AAA), Ketan (AAB), Kepok (ABB) and Klutuk Wulung
(BB). Plantlets were gently uprooted and only those with healthy roots will be used for experiments
by dipped in the Foc suspension (10
6
conidia/mL) for 5 min before replanted into cups containing
sterile sand and placed in the trays for maintenance and observation. Plantlets were watered
everyday and fertilized using nutrient solution (Hyponex
) every week.

Evaluation
Disease symptoms on leaves were recorded after the first two weeks, four weeks. Final
evaluation was observed at fifth week based on the leaf symptom index (LSI) and rhizome
discolouration index (RDI) (Mohamed et al., 2001).
Scales for leaf symptom index (LSI) were:
1. No streaking or yellowing of leaves. Plant appeared healthy
2. Slight streaking and/or yellowing of lower leaves
3. Streaking and/or yellowing of most of the lower leaves.
4. Extensive streaking and/or yellowing on most or all of the leaves.
5. Dead plant.
Scales for rhizome discolouration index (RDI) were:
1. No discoloration of tissue of stellar region of rhizome or surrounding tissue.
2. No discoloration of stellar region of rhizome; discoloration at junction of root and rhizome.
3. Trace to 5% of stellar region discolored.
4. 6-20% of stellar region discolored.
5. 21-50% of stellar region discolored.
6. More than 50% of stellar region discolored.
7. Discoloration of the entire rhizome stele.
8. Dead plant.
After collecting data of LSI and RDI, the overall Disease Severity Index (DSI) for leaf
symptoms and rhizome discoloration for each accession was calculated as follows:

Furthermore DSI of LSI and RDI were translated into four categorize; resistant, tolerant, susceptible
and highly susceptible (Table 1).

Table 1. Translation of DSI scales

DSI Scales for LSI DSI Scales for RDI Translation
1 1 Resistant
Between 1.1 and 2 Between 1.1 and 3 Tolerant
Between 2.1 and 3 Between 3.1 and 5 Susceptible
Between 3.1 and 4 Between 5.1 and 8 Highly susceptible

th

Early Evaluation of Banana Accessions toward Fusarium Wilt VCG 01213/16 (TR4)
Susceptible cultivar Ambon Hijau produced disease symptom within two weeks after
inoculation, with leaves chlorosis were started from older leaves to the younger leaves. Tolerant
cultivar Klutuk Wulung produced no symptom on leaves until five weeks after inoculation. The DSI
of both LSI and RDI of five accessions and their susceptibility or tolerance status are shown in
Table 2.

Table 2. The status of susceptibility or tolerance of five banana accessions

Samples
Calcuta-4 Ketan Klutuk Wulung Ambon Hijau Kepok
LSI RDI LSI RDI LSI RDI LSI RDI LSI RDI
1 1 1 1 1 1 1 2 4 2 2
2 1 1 1 1 1 1 2 2 1 1
3 1 1 1 1 1 1 1 1 1 1
4 1 1 3 3 1 4 4 5 1 1
5 1 1 2 3 1 1 2 4 1 1
6 1 1 2 2 1 1 2 5 1 1
7 3 3 2 3 1 1 3 5 1 1
8 1 1 1 1 1 1 2 4 1 1
9 2 3 2 3 1 3 2 5 1 1
10 1 1 1 1 1 1 2 4 1 1
11 1 1 1 1 1 1 2 3 1 1
12 1 1 1 1 1 1 2 3 2 2
DSI 1.25 1.33 1.50 1.75 1. 00 1.42 2.17 3.75 1.17 1.17
Status Tolerant Tolerant Tolerant Susceptible Tolerant
Notes: LSI = Leaf Symptom Index
RDI = Rhizome Discoloration Index
DSI = Disease Severity Index

Base on DSI of both LSI and RDI (Table 2), all accessions except Ambon Hijau were
categorized as tolerant. Only one inoculated plant of Ambon Hijau had no symptom, while others
showed symptom on leaves (LSI from 2 to 4) and rhizome (RDI from 2 to 5) (Figure 1B). Ambon
Hijau is the member of Cavendish subgroup, which is naturally susceptible to Foc TR4. This finding
was consistent with Hermanto et al. (2011), reported that 81% Foc-infected Ambon Hijau in
Indonesia was caused by TR4 (VCG 01213/16). External symptom of infected leaves and internal
symptom of Ambon Hijau were shown at Figure 1B. Meanwhile, only two out of twelve plants of
Calcuta-4 showed Foc symptoms (DSI of LSI=1.25 and RDI=1.33, respectively) and the status of
this accession was tolerant (Figure 1C). Calcuta-4 is wild-seeded species (Musa acuminata sp.
burmanica) and they are often used for Fusarium wilt resistant breeding program (Tomekpe et al.,
2004).
Five out of twelve plants of Ketan showed symptom on leaf (LSI from 2 to 3) and rhizome
(RDI from 2 to 3), however, DSI values of LSI and RDI were translated as tolerant (Figure 1E).
Ketan also showed tolerant to Foc in some areas in Lampung, West Sumatera and West Java.
Ketan had some synonyms in some places; Janten (Lampung), Jantan (West Sumatera), Uli (West
Java), and Ketip (Nusa Tenggara Barat). This cultivar is popular as cooking banana. An interesting
occurrence was shown by Klutuk Wulung. Two out of twelve plants produced symptom on rhizome
(RDI=3), nevertheless, all plants showed no symptom on leaves (Figure 1A), therefore, DSI of LSI
and RDI of this accession was translated as tolerant. Klutuk Wulung is seeded Musa balbisiana and
scattered in Java, which usually people use leaves of it for wrapper and male bud flower for
vegetable.
th
Another tolerant accession was Kepok, which two out of twelve plants showed symptom
on leaves and rhizome (Figure 1D), and translation of DSI was tolerant. Kepok is very popular
cooking banana and grows in whole part of Indonesia. Cases of infected plant of Kepok were found
in West Java, Yogjakarta, Central Kalimantan and South Kalimantan. Kepok was not only infected
by VCG 01213/16 (TR4), but also VCG 0120 and 01218 (Hermanto et al., 2011).

Figure 1. External (leaves) and internal (rhizome) symptoms of Fusarium oxysporum f.sp. cubense VCG
01213/16 on Klutuk Wulung (A), Ambon Hijau (B), Calcuta-4 (C), Kepok (D) and Ketan (E).

Resistance Mechanisms of Plant to Fusarium Wilt Disease
Resistance mechanism of plant against pathogen was started before the infection of
pathogen into plant tissues. Fusarium oxysporum f.sp. cubense infects banana plant through root
system. Since conidia attach hairy roots, they will germinate and penetrate into the epidermal cells
of roots. Roots of resistant cultivar produce exudates that inhibit germination and growth of conidia;
otherwise, exudates from roots of susceptible cultivar induce germination and growth of conidia (Li
et al., 2011).
Fungal pathogen is capable to penetrate plant roots through invading root epidermal cells
directly, epidermal cell of root caps and elongation zone, natural wound in the lateral root base.
During invasion, fungal hyphae produce cell wall degradation enzymes and penetrate to intercellular
space, grow and develop branches and penetrate to other cells. Besides enzymes, fungal pathogen
also produces micotoxins such as fusaric acid and beauvericin that affect trans-membrane electric
potential, electrolyte leakage and respiration root cells (Pavlovkin 2006). Cell membrane damage
causes the production of reactive oxygen species (ROS) and elicit the production of antioxidants
such as superoxide dismutase (SOD), catalase (CAT), peroxidase (POD) (Kuzniak 2001), and
transduction signal molecules that will trigger the production of pathogenesis related proteins such
A B
C
D
E
th
as chitinase and -1,3-glucanase. These enzymes will degrade fungal cell wall and inhibit growth
and development of pathogen in the plant cells (Wu et al. 2008).
The case in Klutuk Wulung, which infection symptom appeared in the rhizome but no
symptom on the leaves (Figure 1A) indicated that resistance mechanism of plant against pathogen
occurred. The development of fungi was localized only in part of rhizome and blocked for further
expansion.
This evaluation technique was adequate for screening of Fusarium wilt resistant cultivars
and the expression of the disease can be obtained within 6-8 weeks. Using small plants for
evaluation can reduce space requirement when compared to field evaluation.

References

Chand R, D Sen, KD Prasad, AK Singh, BM Bashyal, LC Prasad and K Joshi. 2008. Screening for disease
resistance in barley cultivars against Bipolar sorokiniana using callus culture method. Indian J Exp Biol.
46:249-253.
Hadrami AE, AE Idrissi-Tourane, ME Hassni, F Daayf, IE Hadrami. 2005. Toxin-based in-vitro selection and its
potential application to date palm for resistance to the bayoud Fusarium wilt.C. R. Biologies 328:732
744.
Hermanto C, A Sutanto, Jumjunidang, HS Edison, JW Daniells, WTO Neill, VGO Sinohin, AB Molina and P
Taylor. 2011. Incidence and distribution of fusarium wilt disease of banana in Indonesia. Proc Int ISHS-
ProMusa Symp on Global Perspective on Asian Challenges. Acta Hort. 897:313-322.
Kuzniak E. 2001. Effects of fusaric acid on reactive oxygen species and antioxidants in tomato cell cultures. J
Phytopathol 149(10):575-582.
Li C, S Chen, C Zuo, Q Sun, Q Ye, G Yi and BZ Huang. 2011. The use of GFP-transformed isolates to study
infection of banana with Fusarium oxysporum f. sp. cubense race 4. Eur J Plant Pathol. 131:327-340.
Mohamed AA, C Mak, KW Liew, and YW Ho. 2001. Early evaluation of banana plant at nursery stage for
Fusarium wilt tolerant. In: AB Molina, NH Masdek, KW Liew, Eds. Banana Fusarium Wilt Management:
Toward sustainable cultivation, Los Banos, INIBAP-ASPNET. Pp:174-185.
Pavlovkin J, I Mistrkov, M Luxov, I Mistrk. 2006. Effects of beauvericin on root cell transmembrane electric
potential, electrolyte leakage and respiration of maize roots with different susceptibility to Fusarium. Plant
Soil Environ. 52(11):492498.
Pegg KG, Moore NY, Sorensen S. 1993. Fusarium wilt in the Asian Pacific region. In: Valmayor RV, Hwang SC,
Ploetz RC, Lee SW, Roa NV, eds. Procceeding of International Symposium Recent Developments in
Banana Cultivation Technology. Los Baos: International Network of Banana and Plantain/ASNET.
Pp:225-269.
Vbov L and A Lebeda. 2005. In Vitro Selection for Improved Plant Resistance to Toxin-Producing Pathogens.
J Phytopathol. 153(1):52-64
Tomekpe K, C Jenny, JV Escalant. 2004. A review of conventional improvement strategies for Musa. Info Musa
13(2): 2-6.
Wu HS, XM Yin, DY Liu, N Ling, W Bao, RR Ying, YY Zhu, SW Guo, QR Shen. 2008. Effect of fungal fusaric
acid on the root and leaf physiology of watermelon (Citrullus lanatus) seedlings. Plant and Soil 308: 255-
266.

th
Response of Plant Roots to Drought Stress

Atsushi Kato, Saki Hoshiyasu, Akiho Yokota and Kinya Akashi
*

Graduate School of Biologiccal Sciences, Nara Institute of Science and Technology
*Corresponding author: Graduate School of Biologiccal Sciences, Nara Institute of Science and Technology,
8916-5 Takayama, Ikoma, Nara, 630-0192 Japan
Tel.: +81 743 72 5561; fax: +81 743 72 5569.
[email protected]

Abstract

Around the world, terrestrial plants are strongly affected by abiotic stresses such as drought, high or low
temperatures, high light and salt stress. Among them, drought is one of the major factors limiting distribution and
productivity of plants. Understanding the mechanisms for drought resistance in plants is important for breeding
new crop varieties which can grow under water deficit conditions. In particular, plant root plays pivotal roles in
water uptake and maintenance of water status of plants, thus is an important research target for plant
physiologists and molecular biologists. Responses of plant roots to drought have been extensively investigated
in model plants such as Arabidopsis, which have offered basic knowledge on the molecular mechanisms
underlying the multilateral physiological responses in the roots. Moreover, recent physiological and molecular
studies on drought-resistant plants have shed lights on how these xerophytes cope with severe water deficit
conditions by developing unique survival strategies.

Keywords: root development, drought stress, abscisic acid, xerophyte, wild watermelon

Morphological changes of roots in response to drought stress

Drought stress severely inhibits plant growth (Larcher, 1995). However, development of
root is usually less affected than that of shoot under drought. In maize, it is reported that root growth
is maintained at lower water potentials, while shoot growth is completely inhibited (Sharp et al.,
2004). This report also showed that elongation activity is highly retained in root tip regions under
water deficits. On the other hand, in the case of Brassicaceae species including Arabidopsis,
inhibition of primary root elongation under drought is accompanied with morphogenetic
differentiation process in the lateral roots. In this process, lateral roots remain short, hairless and
often take a tuberized shape with concomitant accumulation of starch and proline (Vartanian et al.,
1994; Xiong et al., 2006). This so-called short-roots then switch to a dormant mode under
prolonged drought periods, until the resume of growth upon rehydration conditions (Wasilewska et
al., 2008). These observations therefore offer an illustrative example on the flexibility of root system
architecture in plants under fluctuating water availability in the soils.

Abscisic acid (ABA) signaling and root morphogenesis

ABA is one of the major plant hormones which mediate adaptation of plants to
environmental stresses. Many plants synthesize a large quantity of ABA in every tissue under stress
(Shinozaki et al., 2003). In the leaves, ABA is well known to stimulate stomatal closure and thus
reduce transpirational loss of water under drought. In the roots, on the other hand, ABA inhibits
elongation of primary roots (Leung et al., 1997; Bai et al., 2009) and decreases a number of lateral
roots (Xiong et al., 2006). Moreover, ABA is shown to be implicated in the development of the
short-roots (Schnall and Quatrano, 1994). Furthermore, analysis of Arabidopsis mutants revealed
that ABA-deficiency inhibits morphological changes of roots in response to the stress, which
impaired stress resistance in these mutants. It is suggested that ABA and ABA signaling elements
th
are important factors for regulating morphological changes of the roots under drought stress
(Wasilewska et al., 2008).

Compatible solutes in the roots

In many plant species, responses to drought stress involve changes in the fluxes of
specific metabolic pathways, which lead to the accumulation of compatible solutes such as sugar
derivatives and amino acids. Previous studies suggested that proline accumulation in the roots
contributes to the osmotic adjustment and fortification of water uptake (Sharp et al., 1990; Voetberg
and Sharp, 1991). In a recent study using Arabidopsis mutants impaired in proline metabolism, it is
demonstrated that proline biosynthesis, transport and degradation are regulated in tissue- and
stage-specific manners during drought (Sharma et al., 2011). Under drought condition, proline is
mainly synthesized in photosynthetic tissue, and a part of the proline is transported to root
meristems, which is further catabolized to various metabolites to support continued growth at low
water potential. Arabidopsis mutants deficient in ABA biosynthesis show impaired proline
metabolism and root growth elongation under water deficits, which is reversed by exogenous ABA
(Sharma et al., 2011). These observations suggested that proline metabolism is partly regulated by
ABA signaling pathway under drought, and these molecular networks coordinately contribute to the
adaptation response of plants under stress conditions.

Root tropism under drought

In response to environmental signals, plants exhibit tropism to control the direction of their
growth. Root system development is largely directed by the interaction of gravitropism and
hydrotropism, which are the responses to gravity and moisture gradient, respectively (Gilroy and
Masson, 2008). Gravitropism is dominantly orientated on primary roots, which is mediated by
sedimentation of starch anchors in the amyloplasts of columella cells. The lateral gradient of auxin
in the root cap is also known to be implicated in the root gravitropism. In water-stressed roots,
hydrotropism is accompanied by the rapid degradation of amyloplasts in columella cells, which
reduces responsiveness to gravity (Takahashi et al., 2003; Eapen et al., 2005). Recent genetic
analysis in Arabidopsis revealed that hydrotropism is mediated by novel factors such as MIZ1 and
GNOM, the latter encoding guanine-nucleotide exchange factor for ADP-ribosylation factor-type G
protein (Kobayashi et al., 2007; Miyazawa et al., 2009), suggesting that GNOM-mediated vesicular
trafficking plays a pivotal role in hydrotropism.

Root development in xerophytes

Plants which survive in water-deficit environments are called xerophytes, which develop
unique drought resistance mechanisms (Wickens, 1998; Graham and Nobel, 1999; Akashi et al.,
2008). Most xerophytes are characterized by their deep root system architecture. A global-scale
investigation of 253 woody and herbaceous plant species reported that plants in the arid and semi-
arid regions have more developed roots, with an average of 9.52.4 m for desert, and 15.05.4 m
for tropical grassland/savanna, which are deeper than those for more humid regions such as
temperate deciduous forest (2.90.2 m), temperate grassland (2.60.2 m) and tundra (0.50.1 m)
(Canadell et al., 1996). Notably, maximum rooting depth was found to be 68 m for Boscia
albitruncas in the central Kalahari Desert. These results illustrated that development of deep root
system is advantageous for reaching to the deep water table in the soils, thereby enabling the
survival in the water-limiting environments.
Interestingly, some xerophytes are characterized by their very shallow root system
architecture (Graham and Nobel, 1999). For example, African baobab (Adansonia digitata) reaches
to a height of 25 m with a trunk of up to 10 m diameter; nevertheless, roots of mature trees are
th
significantly shallow and rarely elongate beyond 2 m (Sidibe and Williams, 2002). Similarly, cactus
(Opuntia ficus-indica) and agaves (Agave deserti) develop shallow and broad root system in which
lateral roots are extensively produced. It has been discussed that these shallow roots are
advantageous for capturing water derived from light rains, which are notorious for their infrequency
in arid regions. These observations therefore suggest that contrasting strategies are employed by
various xerophytes, to survive in the competitive environments for water resources.

Wild watermelon as a xerophyte model to study root response under drought

Deep root system observed in xerophytes is a favorable trait for future molecular breeding
program towards water-saving agriculture. However, molecular mechanisms underlying this trait
have not been fully elucidated. Wild watermelon is a xerophyte inhabiting the Kalahari Desert in
Botswana, despite carrying out C
3
-type photosynthesis (Kawasaki et al., 2000; Miyake and Yokota,
2000), therefore offers an interesting model for how C
3
plants can cope with severe drought
conditions. Previous physiological and molecular analyses demonstrated that root development of
wild watermelon is significantly enhanced at the early stage of drought stress, which is
accompanied with a dynamic change in the root proteome in this plant (Yoshimura et al., 2008).
Drought-induced proteins include those for root morphogenesis such as actin and -tubulin. Various
enzymes for carbon/nitrogen metabolisms such as triosephosphate isomerase, malate
dehydrogenase and methionine synthase are also induced under the stress, suggesting a global
change in the cellular metabolism in the roots to support root growth at the early stage of drought
stress. Interestingly, further changes in root proteome are observed at the later stage of drought
stress, where factors for stress tolerance such as lignin synthesis-related proteins and molecular
chaperones are preferentially induced at this stage. These results, therefore, suggested the
presence of complex molecular networks for regulating abundance of respective proteins in this
plant, in a temporally-programmed manner.
Towards understanding the molecular mechanisms for developing deep root system,
experimental systems for exploring genetic resources in a given xerophyte should offer great
opportunities to characterize genes involved in their root growth. A system for genetic engineering
has been recently established in wild watermelon, where hairy root transformation technique
enables to integrate a given foreign gene construct to both wild and domesticated varieties of
watermelon (Kajikawa et al., 2010). Moreover, generation of a large-scale EST database, as well as
transcriptome analysis are ongoing for wild watermelon, which should offer valuable platforms for
screening and mining useful genes in this xerophyte. It is anticipated that these approaches would
unravel the molecular mechanisms of root vigor in this xerophyte under drought.

References

Akashi K, Yoshimura K, Nanasato Y, Takahara K, Munekage Y and Yokota A. 2008. Wild plant resources for
studying molecular mechanisms of drought/strong light stress tolerance. Plant Biotechnol. 25: 257-263.
Bai L, Zhang G, Zhou Y, Zhang Z, Wang W, Du Y, Wu Z and Song CP. 2009. Plasma membrane-associated
proline-rich extensin-like receptor kinase 4, a novel regulator of Ca signalling, is required for abscisic
acid responses in Arabidopsis thaliana. Plant J. 60: 314-327.
Canadell J, Jackson RB, Ehleringer JR, Mooney HA, Sala OE and Schulze ED. 1996. Maximum rooting depth of
vegetation types at the global scale. Oecologia 108: 583-595.
Eapen D, Barroso ML, Ponce G, Campos ME and Cassab GI. 2005. Hydrotropism: Root growth responses to
water. Trends Plant Sci. 10 :4450.
Gilroy S and Masson PH. 2008. Plant tropisms. Blackwell Publishing. Iowa. USA. Pp123-129.
Graham EA, Nobel PS.1999. Root water uptake, leaf water storage and gas exchange of a desert succulent:
implications for root system redundancy. Ann. Bot. 84: 213223.
th
Kajikawa M, Morikawa K, Abe Y, Yokota A and Akashi K. 2010. Establishment of a transgenic hairy root system
in wild and domesticated watermelon (Citrullus lanatus) for studying root vigor under drought. Plant Cell
Rep. 29: 771-778.
Kawasaki S, Miyake C, Kohchi T, Fujii S, Uchida M and Yokota A. 2000. Responses of wild watermelon to
drought stress: accumulation of an ArgE homologue and citrulline in leaves during water deficit. Plant
Cell Physiol. 41: 864873.
Kobayashi A, Takahashi A, Kakimoto Y, Miyazawa Y, Fujii N, Higashitani A and Takahashi H. 2007. A gene
essential for hydrotropism in roots. Proc. Natl. Acad. Sci. USA. 104: 4724-4729.
Larcher W. 1995. Physiological plant ecology. Springer-Verlag. Berlin, Heidelberg, New York. Pp 277.
Leung J, Merlot S and Giraudat J. 1997. The Arabidopsis ABSCISIC ACID-INSENSITIVE2 (ABI2) and ABI1
genes encode homologous protein phosphatases 2C involved in abscisic acid signal transduction. Plant
Cell 9: 759771.
Miyake C and Yokota A. 2000. Determination of the rate of photoreduction of O
2
in the water-water cycle in
watermelon leaves and enhancement of the rate by limitation of photosynthesis. Plant Cell Physiol. 41:
335343.
Miyazawa Y, Takahashi A, Kobayashi A, Kaneyasu T, Fujii N and Takahashi H. 2009. GNOM-mediated
vesicular trafficking plays an essential role in hydrotropism of Arabidopsis roots. Plant Physiol. 149: 835-
840.
Schnall JA, Quatrano RS. 1992. Abscisic acid elicits the water-stress response in root hairs of Arabidopsis
thaliana. Plant Physiol. 100: 216218.
Sharma S, Villamor JG and Verslues PE. 2011. Essential role of tissue-specific proline synthesis and catabolism
in growth and redox balance at low water potential. Plant Physiol. 157: 292-304.
Sharp RE, Hsiao TC and Silk WC. 1990. Growth of the maize primary root at low potentials. 2. Role of growth
and deposition of hexose and potassium in osmotic adjustment. Plant Physiol. 93: 1337-1346.
Sharp RE, Poroyko V, Hejlek LG, Spollen WG, Springer GK, Bohnert HJ and Nguyen HT. 2004. Root growth
maintenance during water deficits: physiology to functional genomics. J. Exp. Bot. 55: 23432351.
Shinozaki K, Yamaguchi-Shinozaki K and Seki M. 2003 Regulatory network of gene expression in the drought
and cold stress responses. Curr. Opin. Plant Biol. 6: 410417.
Sidibe M and Williams JT. 2002. Baobab, Adansonia digitata L. Fruits for the future 4. International centre for
underutilised crops. Chichester. England. Pp 15.
Takahashi N, Yamazaki Y, Kobayashi A, Higashitani A and Takahashi H. 2003. Hydrotropism interacts with
gravitropism by degrading amyloplasts in seedling roots of Arabidopsis and radish. Plant Physiol. 132,
805810.
Vartanian N, Marcotte L and Ciraudat J. 1994. Drought rhizogenesis in Arabidopsis thaliana, differential
responses of hormonal mutants. Plant Physiol. 104: 761767.
Voetberg GS, and Sharp RE. 1991. Growth of the maize primary root at low water potentials 3. Role of
increased proline deposition in osmotic adjustment. Plant Physiol. 96: 1125-1130.
Wasilewska A, Vlad F, Sirichandra C, Redko Y, Jammes F, Valon C, Frey N and Leung J. 2008. An update on
abscisic acid signaling in plants and more. Mol. Plant 1:198217.
Wickens GE. 1998. Ecophysiology of economic plants in arid and semi-arid lands. Springer, Berlin, Germany.
Xiong L, Wang R, Mao G and Koczan JM. 2006. Identification of drought tolerance determinants by genetic
analysis of root response to drought stress and abscisic acid. Plant Physiol. 142: 1065-1074.
Yoshimura K, Masuda A, Kuwano M, Yokota A and Akashi K. 2008. Programmed proteome response for
drought avoidance/tolerance in the root of a C
3
xerophyte (wild watermelon) under water deficits. Plant
Cell Physiol. 49: 226241.

th
Growth and Development Characteristics of Hoya multiflora Blume

Sri Rahayu

Bogor Botanical Gardens, Indonesian Institute of Sciences
Jl. Ir. H. Juanda 13 Bogor, Indonesia
[email protected]

Abstract

Hoya multiflora is one of the valuable germplasm in Indonesia utilized as ornamental and medicinal plants. This
epiphytic plant faces problems in decreasing habitat, while the culture technique of this species has not
established yet in Indonesia. It is important that all useful plant can be maintained to prevent the exploitation
from the wild. Biological data on growth and development will provide a guideline to establish good culture
techniques. The research aim was to investigate the growth and development of the seedlings of Hoya multiflora
in two different conditions and growing media i.e. (1) in the natural habitat at the Bodogol Research Station of
Gunung Gede Pangrango National Park, and (2) in a shade house of the Bogor Botanical Gardens as artificial
habitat. Three different growing media was used in observation, i.e. (1) its phorophytes observed at natural
habitat, (2) organic matter conducted at the shade house (3) tree fern log conducted at the shade house. The
results showed that general, the growth and development of Hoya multiflora started by seed germination
characterized by opened cotyledon, seedling establishment characterized by formation of alternate leaves
arrangement, followed by growth of young plant characterized by formation of opposite leaves arrangement,
growth and development of adult plant, flowering and fruiting. The critical point was at the seedling
establishment phase, which best reached at the cocopeat medium. When the seedling established and
developed to adult, there were no differences at the different growing media used. The best recruitment, growth
and development of Hoya multiflora was at the cocopeat media located in the shade house.

Keywords: Gede Pangrango National Park, Hoya multiflora, growth and development, Bogor Botanical Gardens

Introduction

Hoyas (Apocynaceae: Asclepiadoideae) are becoming increasingly popular as ornamental
plant, particularly in Europe, USA and Australia (Goyder, 2008). The international trade of this
genus is increasing, but their existence in the nature obtains less attention, eventhough the
conservation status was not state yet. In contrary, their habitat as epiphyte rapidly decrease mainly
by the deforestation i.e. logging, burning, and forest conversion into plantation. The rapid increase
on palm oil plantation especially prompted by the potential use as biofuel will multiply habitat lost for
Hoyas as epiphyte.
The genus naturally originated from India, distributed to Australia and the Pacific Islands,
with the greatest diversity is now found in South East Asia, particularly in Indonesia (Kleijn &
Donkelaar, 2001; Wanntorp, 2006). There are about 150-200 Hoya species in the world (Hoffman
et all, 2002), 50-60 of which are in Indonesia (Rahayu, 2001). H. multiflora widely distribute from
India to New Guinea (Goyder, 2008) from 50-1500 m above sea level (Rahayu et al., 2010). This
species is characterized by its short (non vein) plant, leathery (non succulent) oblong leaves and
arrow head form white corona with yellow tip of the corolla. Flowers arranged in umbel appear at
interpetiolar node. This plant produces white latex from all of its part.
Some indigenous people in the country have been utilizing some species of Hoyas as
traditional medicine. The uses are for treat burns, cuts, convulsions, coughs, asthma, pneumonia,
elephantiasis, encephalistis, fractures, gonorrhea, hemorrhoids, inflammation, insect
bites/poisonous fish stings, orchitis, phthisis (tuberculosis), Pyroderma (skin disease caused by
microorganisms), rashes, rheumatism/arthritis, swellings, traumatic injures/wounds, stomach and
th
intestinal ailments, and childbirth tonic (Zachos, 1998). A recent study shows their high potential as
insecticide to the Dengue mosquito. Hoya multiflora Blume is one of the economic important as
ornamental plant, and has been used traditionally as medicine, particularly to treat arthritis-
rheumatism (Burkill, 2002) and stomach/intestinal ailments (Ambasta, 1986). The active compound
of this plant unrevealed yet, but it could be Indomethacine like compound. Indomethacine, a
common non-steroidal anti inflammatory drug (NSAID), has been used for more than 30 years to
treat symptomatic pain of rheumatoid arthritis. Recently, this compound has been tested as a new
class of anti HIV drug (Bourinbaiar & Lee-Huang, 1994) and seems to be specific since no toxicity
at clinical doses.
Despite of their high economic importance, little is known about their cultivation especially
in Indonesia. As this plant is loved as ornamental plant and has a medicinal property, the
knowledge on its growth and development is needed. The knowledge will be useful for the
cultivation and living collection management for ex- situ conservation purposes. This research
aimed to observe the growth and development characteristics of Hoya multiflora Blume.


The observation on the growth and development characteristics of H. multiflora was
conducted both at their own natural habitat at the Bodogol Research Station, Gunung Gede
Pangrango National Park, West Java and in a shade house at the Bogor Botanical Gardens. There
were 10 mature, 5 young and 3 clumps of seedling observed at Bodogol RS. Observation at the
Bogor Botanical Gardens was focused on the flowering and fruiting time using 20 accession
collected from the Bodogol RS (2004-2006); and seedling growth and development from the fruit
produced (2005). The observation on growth and development conducted at the following
parameters:

Germination
The experiment was conducted at the Bogor Botanical Gardens shade house. The shade
house condition was under the paranet having 75% canopy. The seeds were shown on the 2
different kinds of growing media, namely (1) cocopeat at the plastic plate and (2) tree fern log. The
seeds used were from the harvested mature fresh pod in the green house. Each of 20 seeds were
shown on the media two times. The seedlings were watered daily. Parameters observed were
seedling percentage, time of opened seed coat, time of hypocotyle, time of first leaf appearance,
and time of opposite leaf formation.

Seedling establishment
Observation was conducted using the growing seedling taken from the seed growth
germination experiment. The parameter observed was started at the established seedling growth to
the young plant, recorded by the formation of opposite leaf arrangement.

Growth
The young plant stated as the seedling formed the first opposite leaves. The observation
was done from the growth of shoot and leaf (number of leaf) to the plant formed the first
inflorescence.

Flowering and fruiting
Observation was conducted to record the flower formation, time of flowering, and lower
product. The process of flowering and fruiting were recorded. Observation also made on the fruit
ratio to the number of flower.

th

Generally, the growth and development of Hoya multiflora started from (1) seed
germination characterized by opened cotyledon, (2) seedling establishment characterized by
formation of alternate leaves arrangement, (3) growth of young plant characterized by formation of
opposite leaves arrangement, (4) growth and development of adult plant, (5) to flowering and
fruiting. The process of growth and development at the different condition are as follows:

Germination (in shade house condition)
The germination process of H. multiflora started from seed coat opening, followed by
cotyledone opening until the first leaf forming. H. multiflora evolve the epigeal germination, which
cotyledone above soil surface. According to Copeland & McDonald (2001), there are two
germination types based on location of storage reserves. The research showed that the seed of H.
multiflora grew 2-3 days after showing and had the high viability up to 100% at the cocopeat media.
The seed of H. multiflora was similar to H. parasitica without dormancy (Rahayu & Sutrisno, 2007).
Showing seed at the tree fern media resulted in the lower viability (80%) and took longer time (7-30
days) to germatinate (Table 1). Overall, the germination process was faster at the cocopeat media
than that at the fern tree fern log. There was microclimate different condition between cocopeat
media and tree fern log, especially on the media humidity and water capacity. Cocopeat media was
reported to be able to absorb more water and keep wet for a longer time than the log. The time of
germination is faster at the cocopeat media, as more water stimulate the seed imbibitions. Besides
that, the cocopeat media also provided ready to use nutrient. Media humidity and water content are
the main factors for seed germination. Germination of seed involves the imbibitions of water, a rapid
increase in respiratory, mobilization of nutrient reserves and initiation of growth in the embryo
(Fenner & Thompson, 2006). Water is a basic requirement for germination as it is essential for
enzyme activation, breakdown, translocation and use of reserve storage material (Copeland &
McDonald, 2001).

Table 1. Seed germination of H. multiflora at the two different kinds of media

Media
Seed coat
opening (days)
Cotyledone opening
(days)
First Leaf
Formation (days)
Seed viability
Tree fern log 7-30 14-45 41-60 80
Cocopeat 2-3 5-7 13-20 100

Seedling establishment
The seedling is characterized by alternate leaf formation. Seedling establishment was
reached 12 month after seed germination. Seed on the cocopeat media had sorter time to grow
(Table 2) and the highest establishment (80%). In contrary, at the tree fern log resulted the lowest
growth and establishment (30%). Natural phorophyte was better to support seedling establishment
of H. multiflora compared with the tree fern log media. Tree fern log had the lowest water holding
capacity and nutrient availability compared with the cocopeat media and natural phorophyte. At the
natural phorophyte, the seedling of H. multiflora grew on the ant nest (Rahayu et al, 2010), which
provided nutrient and water holding capacity for the requirement of the H. multiflora to grow. During
the seedling establishment, nutrient requirement increase from the former phase (germination). The
tree fern log had the most limiting factor for seedling establishment of H. multiflora. According to
Fenner & Thompson (2006), factor limiting establishment are competition between seedlings and
abiotic hazards i.e. occurance of physical damage and lack of moisture. The limiting factor at tree
fern log was dominantly by lack of moisture which caused seedling desiccation. Seedling
desiccation is a particularly acute hazard in the branches of trees (epiphytes) and the main cause of
th
seedling mortality (Fenner & Thompson, 2006). While the limiting factor at the natural phorophyte
was dominantly by competition because many seeds were germinated at one hole (ant nest).

Table 2. Time of seedling growth of H. multiflora at different media

Media Number of
alternate
leaves
Time of first opposite
leaf formation
(months)
Plant height at the time
of first opposite leaf
formation (cm)
Successful
seedling
percentage
Tree fern log 12-13 14 2,0 18,4 1,2 30
Cocopeat 12-13 12 1,0 25,6 0,7 80
Natural phorophyte 13-17 13 1,5 19,8 1,5 50

Young to adult
At this phase, plant growth was determined after seedling establishment, characterized by
opposite leaf formation. At this phase, growth and development of plant were dominated by the
increase in the node number followed by the increase in leaf number. There are two leaves
(opposite formation) at each node. The new node emerged at about every one month. When 12
nodes completed (after one year), new branch developed at the shoot base and followed by the
emergence of peduncle. The time at this phase was quite similar to the occurance at different
growing media (Table 3). This condition indicated the stability of the plant after seedling
establishment phase.

Table 3. Growth and development of H. multiflora at different growing media

Media
Time of node
growth
(days)
Number of opposite
leaves node at the
first flowering
Time of first
flowering
(Months after
germination)
Plant height
at the first
flowering
(cm)
Number of
branch at
the first
flowering
Tree fern log 30 9 121 20-28 305 2
Cocopeat 28 7 121 18-30 302,5 0-2
Natural phorophyte 29 8 12 1 18-30 4010 0-2

Flowering and fruiting
All plant at the different growing media and location developed and produced flowers and
fruit. The time of flower and fruit development was quite similar (Table 4). This condition indicated
the time for seedling establishment and development to adult plant, when the reproduction process
occured, i.e. plant produced flower and fruit. It means all growing media provided nutrient and basic
requirement for the plant development. While fruiting process occurred at both different
environments i.e. at the shade house condition and at the natural habitat. The pollination process in
H. multiflora needs the presence of pollinator (Rahayu et all, 2010) and Chasanah (2010) has been
identified that Vespidae was the pollinator of H. multiflora at the Bodogol forest.

Table 4. Flower and fruit development of H. multiflora at different condition

Media
Peduncle
development
(days)
Bud development
(days)
Anthesis
(days)
Percentage of
fruit set
Fruit
development
(days)
Tree fern log 30 10 28 5 14 1 0.01 35 4
Cocopeat 29 9 27 4 14 1 0.01 34 5
Natural phorophyte 30 11 29 5 14 1 0.01 36 5

th
References

Ambasta S.P. 1986. The usefull plants of India. Publ. & Inform. Dir. Council of Scientific and Industrial Research.
New Delhi, India
Bourinbaiar AS; Lee-Huang, S. 1995. The non steroidal anti inflammatory drug, Indomethacin, as an inhibitor of
HIV replication. FEBS Letters 360 (1):85-88
Burkill IH. 2002. A dictionary of economic product of Malay Peninsula. Vol. 2. Ministry of Agriculture Malaysia,
Kuala Lumpur.
Chasanah LR. 2010. Diversity and frequency of pollinator insect visit and its influence to the fruit set in Hoya
multiflora. [S2 thesis]. Bogor Agric. Univ. Bogor
Copeland, LO and McDonald, MB. 2001. Principles of seed science and technology. 4
th
Ed. Kluwer Acad. Publ.
London
Fenner, M and Thompson, K. 2006. The ecology of seeds. Cambridge Univ. Press, Cambridge
Goyder D. 2008. Hoya multiflora Blume. Curtis Bot. Magazine 7(1): 3-6.
Hoffman C, van Donkelaar R, Albers F. 2002. Hoya R.Br. In Albes F & Meve U (Eds.) : Illustrated Handbook of
Succulent Plants: Asclepiadaceae. Berlin: Springer-Verlag. pp: 146 - 158
Kleijn D. and R van Donkelaar. 2001. Notes on The Taxonomy and ecology of the genus Hoya (Asclepiadaceae)
in Central Sulawesi. Blumea 46: 457 -483
Rahayu S. 2001. Genetic diversity of Hoya in Sumatra. [S2 thesis]. Bogor Agric. Univ. Bogor
Rahayu S, Sutrisno (2007) Potency of Hoya seed in propagation and conservation: case study on Hoya
parasitica Wall. Buletin Kebun Raya10 (2) : 33-39 [Indonesian]
Rahayu S, Kusmana C, Abdulhadi R, Jusuf M, Suharsono (2010) Distribution of Hoya multiflora Blume at
Gunung Gede Pangrango National Park, Indonesia. Journal of Forestry Research 7 (1): 42-52
Wanntorp L, Koycan A, Renner S (2006) Wax plants disentangled: A phylogeny of Hoya (Marsdenieae,
Apocynaceae) inferred from nuclear and chloroplast DNA sequences. Molecular Phylogenetics and
Evolution 39: 722-733
Zachos E. 1998. Practical uses of various Hoya species. The Hoyan 19 (4)/20 (1): part II: 6-10/3-8

th
Effects of High Water Table and Waterlogging on Sunflower Growth, Yield
and Seed Quality

Satoko Yasumoto
a,*
, Yukari Terakado
b
, Morio Matsuzaki
a

a
Biomass production and processing team, National Agricultural Research Center, Tsukuba, Japan,
b
Ibaraki Prefectural Agricultural Experimental station, Daitoku, Ryugasaki, 301-0816, Japan
* Corresponding author: Institute of National Agricultural Research Center, 3-1-1 Kannondai, Tsukuba, Japan,
Tel./fax: +81 298 838 7038
[email protected]

Abstract

Understanding the response of sunflower (Helianthus annuus L.) to high water table and waterlogging is
important for successful cultivation in monsoon Asia. We examined the physiological responses of sunflower
cultivars to these conditions. In the rotational paddy field, where the water table depth was shallow, growth of the
plant was suppressed, seed yield was decreased and harvest quality was deteriorated. In the artificially inclined
field, the ditch surrounding the sloped plot was constantly filled with water, the growth of plant and oil
concentration were decreased significantly when the water table was shallower than about 30 cm. In the pot
experiment, where water was logged at different growth stages, the relationship between seed yield and the
underground dry weight was significant (r = 0.87, p < 0.01). In cultivars with vigorous growth of underground
part, many adventitious roots were appeared. Screening for the appearance of these roots may be an effective
way to select sunflower cultivars that are capable of tolerating high water table and tolerating waterlogged
conditions and avoiding decreases in seed and oil yield.

Keywords: sunflower, water table, waterlogging, seed quality, adventitious roots

Introduction

Regarding the effects of short-term waterlogging on sunflower, there were some reports
about that to the growth, yield and quality. Orchard and Jessop (1984) reported on sunflower and
sorghum that growth stages were greater importance than the duration of waterlogging. And
Orchard and So (1985) reported that waterlogging at the vegetative and floral initiation stages
reduced the root growth and it reduced the water use and nutrient uptake (Orchard et al. 1986).
Grassini et al. (2007) reported waterlogging during grain filling determines direct physiological
responses that decrease grain yield. Regarding the fatty acid, there were some reports on the
factors changing their compositions. The temperature condition was widely reported as one of the
factors. Nagao et al. (1984) and Sobrino et al. (2003) reported that the oleic/linoleic acid ratio was
increased with higher temperature during grain filling. But there are few reports about the effects of
shallow water table to sunflower growth and quality.
We are studying the cultivation of sunflower on rotational paddy field for the purpose of
human consumption, and for the use of bio-diesel fuel. In the field, the shortening of maturing
periods and reductions of stem length, leaf number and disk diameter were observed in many
cultivars. And the decrease of seed yield and oil content, oleic acid composition and the increase of
linoleic acid composition were also observed. The objective of this paper is to elucidate the effects
of shallow water table on the growth, yield and quality and to elucidate the effects of waterlogging in
different stages and in different cultivars of sunflower.

th

Field and pot experiments
Experiments I was conducted in 2007 and 2008 on an artificially sloped plot at Ibaraki
Agriculture Institute (Ryuugasaki, N: 3554, E:14012)The slope had 8.3 m in length and 0.86 m in
height at one end. It could set of 10 rows with different water table. Their water table depths were
from 0 cm to 86 cm in 2007, and from 3.7 cm to 78 cm in 2008. The row spacing was 0.95 m in
2007 and 0.90 m in 2008 and the distance between plants was 0.2 m in both years. The ditch
surrounding the sloped plot was constantly filled with water after establishment of seedling until the
finish of the experiment. Soil moisture content was measured by a soil moisture probe (Profile
Probe PR2, Daiki Rika Kogyo Co. Ltd., Tokyo). Two hybrid varieties were used. One was traditional
type; the name was Hybrid sunflower (Hy.) (Kaneko Seeds Ltd. Gunma), and the other was mid-
oleic type, 63M80 (Pioneer Hi-Bred International, Inc., USA). They were sown on 7 June in 2007
and on 5 June in 2008 as early sowing and on 26 June in 2007 and in 2008 as late sowing. Before
planting, a chemical fertilizer was applied at the rate of N-P
2
O
5
-K
2
O = 8.4-8.4-8.4 g m
-2
, in 2007 and
2008. Root growth of the two cultivars at flowering (22 Aug.) was examined by excavating the whole
root systems of three plants in late sowing block in 2008 at two water depths (3.7 cm and 20.2 cm).
Stem length, leaf nitrogen, number of seeds per a flower disk, flowering date, and maturing date
were measured. Soil moisture content was measured by a soil moisture probe (Profile Probe PR2,
Daiki Rika Kogyo Co. Ltd., Tokyo). Yield of each plot was determined using the same method as
reported by Izquierdo et al. (2002). Thousand kernel weight, oil content and fatty acid composition
were measured by the same method as reported by Yasumoto et al. (2011). All treatments were
replicated two or three times depending on the varieties.
Experiments II was conducted in 2010. It was examined effects of waterlogging on
sunflower at different developmental stages by a pot experiment. The pots were 50 cm long, 65 cm
wide and 45 cm deep. Seven hybrid varieties were used. In the cultivars, 3 were traditional type, 4
were mid-oleic type. Before planting, a chemical fertilizer was applied at the same rate as in
Experiment I. Waterlogging treatments were imposed at different developmental stages,
establishment and flower bud visible. The control was irrigated according to the necessary. Because
the flowering time was delayed by waterlogging at the stage of establishment, the seeds of the
plants for this treatment were sown on 25 May, while the others were sown on 4 June in 2010. The
duration of the waterlogging was the same as in the experiments reported by Wample and Davis
(1975), namely 4 days in each treatment. The parameters as in Exp. I were measured. And root dry
weight and total dry weight were also measured. Yield and seed quality were measured as in Exp. I.
The sampled roots were carefully washed using a colander. The roots and other samples were
dried at 60 C until constant weight (for about 48 hr.) in a forced-air circulation oven, to determine
the dry weight.

Sample and data analysis
Sampled seeds were air-dried. Two g seeds from each sample were crushed and the oil
was extracted with n-butyl alcohol. The measurement of oil concentration and fatty acids
composition in total fatty acid were determined by the method of Caviezel (Pendl et al., 1998) using
a gas chromatograph ( B-820,NihonBchCo.Ltd.,Tokyo ). The concentrations of fatty acids were
calculated from their peak areas. And the percentage of the total fatty acid content was calculated
from their peak areas.

The results were analyzed by ANOVA. All statistical analyses were performed with SPSS
11.0 for Windows (SPSS, 2001). All values are expressed as mean values. Significant differences
were established by the Tukeys test at P<0.05. A correlation was calculated and the significance
levels (P<0.01) are based on the Pearson coefficients.
th
Results

Exp. I. Effects of water table depth on growth, yield and quality
In both years, stem length, disk diameter and seed and oil yield were significantly reduced
with shallower water table. Even in the condition that the depth to water table was 3.7 cm, Hy. grew
more vigorous roots near the ground surface than 63M80 (Fig. 1a-b). Fig. 2 showed the decrease of
leaf nitrogen, number of seeds per a disk, thousand kernel weight, seed yield. That was clearer
upper than about 30 cm of the depth to water table. Oil concentration was also decreased upper
than about 30 cm of the depth to water table. And oil concentration was some higher in early sowing
block. The decrease in oleic acid and the increase in linoleic acid with rising water table were also
somewhat clearer in the plants sown on early sowing block. Their results were shown about same
tendency in 2007 and in 2008.

Figure 1. Root growth of sunflower grown at water table depths of 3.7 cm (left) and 20.2 cm (right). (a) Hy. (b)
63M80.

: Hy., : 63M80 in early sowing, :Hy., : 63M80 in late sowing.

Fig. 2. Growth, Yield and seed quality in the inclined plot in 2007.

a b

0
30
60
90
120
0 30 60 90
S
e
e
d

y
i
e
l
d

(
g

p
l
a
n
t

-
1
)
Water table depth (cm)
0
400
800
1200
1600
0 30 60 90
N
u
m
b
e
r

o
f

s
e
e
d
s
p
e
r

a

d
i
s
k

0
30
60
90
0 30 60 90
T
h
o
u
s
a
n
d

k
e
r
n
e
l

w
e
i
g
h
t

(
g
)
0
20
40
60
0 30 60 90
O
i
l

c
o
n
c
e
n
t
r
a
t
i
o
n

(
%
)
0
2
4
6
8
0 30 60 90
L
e
a
f

n
i
t
r
o
g
e
n

(
%
)
th
0
5
10
15
20
25
30
0 50 100 150 200
S
e
e
d
y
i
e
l
d
(
g
p
l
a
n
t
Plant ength (cm)

Establishment
Flower bud initiation
Control
r=0.60**
0
5
10
15
20
25
30
0 5 10 15
S
e
e
d
y
i
e
l
d
(
g
p
l
a
n
t
Root dry weight (g D.W. plant

-1
)
Establishment
Control
r=0.87**
0
5
10
15
20
25
30
0 5 10 15 20
S
e
e
d
y
i
e
l
d
(
g
p
l
a
n
t
Disk diameter (cm)

Establishment
Control
r=0.82**
Exp. II Effects of waterlogging on sunflower at different developmental stages
There were significant differences between the stages of waterlogging (Table1). The
sunflower was affected by waterlogging (Table1). In many cultivars, seed yield was decreased by
waterlogging at the flower bud initiation stage. The response of waterlogging to root dry weight was
different between cultivars. In many cultivars, their root weight was decreased by waterlogging at
the flower bud initiation stage. In some cultivars, adventitious roots were formed after waterlogging
treatment. The high significant relationship between seed yield and plant characters as the disk
diameter and the root dry weight were observed through the different stages of water logging
treatments (Fig.3).

Table1. Effects of waterlogging treatment on the growth, yield and harvest quality in 2010
Growth stage at
waterlogging
Type Cultivar
Flowering
date
Maturing
date
Ripening
period
(days)
Sum.
Temp.
(
Plant
height
(cm)
Disk
diameter
(cm)
Yield
(g plant
-1
Thousand
kernel
weight
(g)
Oil
concentration
Oleic
acid
Linoleic
acid
Shoot
dry
weight
(g
Root dry
weight
(g
Establishment Trad. Hybrid sunflower July 28 Sep. 2 36 1143 126 13 13.0 24.6 38.7 36.1 50.7 39.5 6.3
North Queen July 28 Aug.29 33 984 121 8 10.6 27.2 25.5 42.1 42.9 28.2 2.4
IS3011 July 28 Aug. 30 34 1009 104 14 17.0 36.7 35.2 40.2 47.7 47.4 6.0
Nusun 63M80 July 28 Sep. 2 37 1170 67 9 7.1 19.5 12.2 68.5 19.0 13.9 2.3
Hysun521 July 26 Aug.26 32 935 89 10 9.4 27.6 30.3 58.0 27.9 29.4 3.9
Hysun 511 July 26 Aug.26 32 945 93 10 13.7 32.9 31.5 67.5 18.9 29.3 3.8
Hysun530 July 25 Aug.26 33 992 115 12 14.9 26.0 34.6 69.3 17.3 34.7 4.6
Trad. Hybrid sunflower July 31 Sep.1 33 1039 102 13 9.8 25.0 33.4 35.1 49.7 41.6 4.2
IS3011 July 30 Aug.28 30 864 79 9 4.4 18.1 28.8 37.9 48.3 33.4 2.9
Nusun 63M80 July 30 Sep.2 35 1124 119 14 8.9 36.6 40.5 72.6 15.1 47.2 5.8
Hysun521 July 29 Aug.28 31 982 89 8 5.9 21.1 29.3 65.0 21.8 26.0 2.1
Hysun 511 July 25 Aug.26 33 962 78 9 11.0 19.5 30.5 67.8 18.3 33.0 3.2
Hysun530 July 30 Aug.25 27 908 72 6 2.1 17.8 29.1 70.5 15.7 8.6 0.8
Control Trad. Hybrid sunflower July 31 Sep.1 34 1080 138 14 19.9 34.2 34.7 38.7 47.1 39.7 5.3
IS3011 July 30 Sep.1 34 1048 121 15 24.2 31.6 37.9 35.2 52.9 54.9 7.9
Nusun 63M80 July 29 Sep.2 36 1141 139 15 23.9 35.8 43.0 72.3 17.6 62.8 10.6
Hysun521 July 29 Aug.31 34 967 114 14 19.3 28.8 37.1 63.2 24.1 62.1 7.1
Hysun 511 July 26 Aug.26 32 761 107 14 20.8 24.6 32.6 61.0 25.9 62.7 6.3
Hysun530 Aug. 1 Aug.31 32 876 113 12 19.4 26.5 30.2 74.2 11.0 61.3 6.4
** ** ** ** ** ** * ns ns ** **
** ** ** ns * ** ** ** ** ns ns
** ** ** ns ns ns ns ns ns ns *
Flower bud
initiation
Stage
Cultivar
StageCultivar

ns, not significant. **, * indicated statistically significant at P<0.01 and 0.05.
ns, not significant. ** indicated statistically significant at P<0.01.
** indicated statistically significant at P<0.01.

Figure 3. Relationship seed yield and plant characters after each water logging treatment.

th
Discussion

In Exp. I, the plant growth and seed yield were reduced with shallower water table while
the oil concentration was highest in the plot with a water table depth of 30 cm. It was quite shallow.
And from this result, it was thought that the growth, yield, and seed quality of sunflower were
affected by soil moisture conditions. In Exp. II, there were differences in the response to
waterlogging between cultivars. In some cultivars, adventitious roots were formed after
waterlogging. Kramer (1951) reported the adventitious roots contributed to plant survival during
flooding. Wample and Davis (1975) reported that adventitious roots formation was one of the
responses to flooding. And Jackson (1955) reported that when the original root system was
flooded, adventitious root developed to prevent injury to the shoot and to promote shoot recovery
from flooding. And in Exp. I, the differences of root growth between cultivars was also observed.
Even in the condition that the depth to water table was 3.7 cm, Hy. grew more vigorous roots near
the ground surface than 63M80. So this difference of appearance of the root was thought to be
related to differences in the ability of these cultivars to tolerate flooding and high water table.
These results of this study suggested that the water management was important for
improving the growth and quality of sunflower. Further research is needed to identify the
physiological mechanisms responsible of sunflower to excess soil moisture.

References

Grassini P., Indaco, G.V., Pereira, M. L., Hall, A. J. and Trapani, N. 2007. Response to short-term waterlogging
during grain filling in sunflower. Field Crops Res. 101:352-363.
Izquierdo, N., Aguirrezabal, L., Andrade, F. and Pereyra, V. 2002. Night temperature affects fatty acid
composition in sunflower oil depending on the hybrid and the phenological stage. Field Crops Res. 77:
115-126.
Jackson, W. T. 1955. The role of adventitious roots in recovery of shoots following flooding of the original root
systems. Am. J. Bot. 42:816-819.
Kramer, P.J. 1951. Causes of injury to plants resulting from flooding of the soil. Plant Physiol. 26:722-736.
Nagao, A. and Yamazaki, M. 1984. Effect of temperature during maturation on fatty acid composition of
sunflower seed. Agric. Biol. Chem.48:553-555.
Orchard, P. W., and Jessop, R. S. 1984. The response of sorghum and sunflower to short-term waterlogging. I.
Effects of stage of development and duration of waterlogging on growth and yield. Plant and soil 81:119-
132.
Orchard, P. W., and So, H. B.1985. The response of sorghum and sunflower to short-term waterlogging. II.
Changes in the soil environment under waterlogged conditions. Plant and soil 88:407-419.
Orchard, P. W., Jessop, R. S. and So, H. B. 1986. The response of sorghum and sunflower to short-term
waterlogging. IV. Water and nutrient uptake effects. Plant and soil 91:87-100.
Pendl, R., Bauer, M., Caviezel, R. and Schulthess, P. 1998. Determination of total fat in foods and feeds by the
Caviezel method, based on a gas chromatographic technique. J. of AOAC International 81 (4): 907-917.
Sobrino, E., Tarquis, A. and Dias, M. C. 2003. Modeling the oleic acid content in sunflower oil. Agron. J. 95:329-
334.
Yasumoto, S., Terakado, Y., Matsuzaki M. and Okada, K. 2011. Effects of High Water Table and Short-Term
Flooding on Growth, Yield, and Seed Quality of Sunflower. Plant Prod. Sci. 14(3): 233-248.
Wample, R. L. and Davis, R. W. 1975. Effect of aeration on the flood-induced formation of adventitious roots and
other changes in sunflower (Helianthus annuus L.). Planta 127: 263-270.

th
Population Genetics of Hoya multiflora at Sukamantri of Gunung Salak,
West Java, Indonesia Based on Isozyme Analysis

Sri Rahayu
a
* and Rochadi Abdulhadi
b

a
Bogor Botanical Gardens, Indonesian Institute of Sciences (LIPI), Jl Ir. H. Juanda 13 Bogor.Indonesia
b
Research Centre for Biology, LIPI, Cibinong Science Centre. Jl Raya Cibinong Bogor, Indonesia
*Corresponding author: Bogor Botanical Gardens, Indonesian Institute of Sciences (LIPI),
Jl Ir. H. Juanda 13 Bogor. Indonesia. Telp/fax 0251-8322187.
[email protected]

Abstract

Hoya multiflora Blume is tropical epiphytic plant reported having some medicinal properties in the rural
communities in Asiatic counties i.e India and Malaysia. In Europe and USA, this plant has been internationally
traded as exotic ornamental plant. The traded plant was directly extracted from the wild habitat, which imply on
the population equilibrium. Population genetic study on epiphytic Hoya multiflora plant has been conducted
using the plant population at Sukamantri at gunung Salak, West Java Indonesia. The study was based on the
isozyme analyses by using PER, EST, MDH, ADH, AAT. The results showed that analyses using POPGENE
software indicated that the genetic differentiation was low, but the estimation on gene flow was high.

Keywords: Hoya multiflora, isozyme, population genetic

Introduction

Hoya multiflora Blume (Apocynanceae:Asclepiadoideae) is one of the economic important
species as ornamental plant, and has been used traditionally as medicine, particularly to treat
arthritis-rheumatism (Burkill, 2002) and stomach/intestinal ailments (Ambasta, 1986). The active
compound of this plant is unrevealed yet, but it is predicted to be Indomethacine like compound.
Indomethacine, a common non-steroidal anti-inflammatory drug (NSAID), has been used for more
than 30 years to treat symptomatic pain of rheumatoid arthritis. Recently, this compound has been
tested as a new class of anti HIV drug (Bourinbaiar & Lee-Huang, 1994) and it seems to be specific
since no toxicity at clinical doses.
The distribution of H. multiflora ranges from India to New Guinea (Goyder, 2008) from 50
to1500 m above sea level (Rahayu et al., 2010). This species is characterized by its short (non
vein) plant, leathery (non succulent) oblong leaves and arrow head form white corona with yellow tip
of the corolla. Flowers is arranged in umbel appear at interpetiolar node. This plant produces white
latex from all of its part (Rahayu 2006). In Europe and USA, this plant has been internationaly
traded as exotic ornamental plant. The traded plant was directly extracted from the wild habitat,
which imply on the population equilibrium.
All of Hoya plant species including H. multiflora are epiphyte. In the natural habitat, the
presence of this plant depends on the presence of host plant, which defined as phorophyte
(Benzing 2008). So this species faces problems in decreasing habitat due to the increase of
deforestation. The decrease on the number of forest tree will imply on the population decrease of
this species, which in turn will imply on the genetic erosion toward extinction. Little is known about
population genetic of this species. The study on population genetic will provide data to support
conservation strategies and development of this species as economic plant. Genetic markers
generally have contributed to the study of plant biology by providing methods for detecting genetic
differences among individuals. There are some important ecological topics which often use
allozymes as powerful markers, especially to assess the genetic differentiation among populations
th
(Zeidler, 2000). This research was aimed to assess the genetic differentiation of Hoya multiflora
populations at Sukamantri of gunung Salak, West Java Indonesia based on the isozyme analysis.


Sample source
A total 50 samples were obtained from three populations of H. multiflora from Sukamantri.
All populations were located at 700 800 m above sea level. Population 1 was from Buper
Sukamantri with the total sample of 16, population 2 was from Tapos with the total sample of 16 and
population of 3 were from Bobojong with the total sample of 18. All of sample were collected as
stem cutting and planted at the greenhouse at Bogor Botanical Gardens as pot plants. After 2
months of acclimation, the plant produced new shoot and young leaves. Young leaves with the size
less than 3 cm long were used as enzyme source.

Isozyme extraction
The method of enzyme extraction followed Soltis and Soltis (1989). Leaves were
processed at the same day they were collected from the plants. Approximately 400 mg of samples
were placed in a mortar, extract buffer were added than it was grinded well. The liquid of extract
was adsorbed by a 0.5 x 0.5 cm filter paper and ready to placed in to the prepared gel.

Electrophoreses
Starch was prepared as follows: equal amounts of the two starch types (16.5 + 16.5 g)
were mixed well and fully suspended in 100 mL the appropriate gel buffer in a flask. The remaining
200 mL of this buffer were brought to a boil before being added to the suspension. The buffer
systems used depended on the enzyme activities to be assayed, and included the following: AAT
(Aminoacid transferase), ADH (Alcohol dehidrogenase), EST (Esterase), PER (Peroksidase), MDH
(Malate dehidrogenase), ACP (Acid phosphatase). The gel were mold to become firm. The wells
(0.5 x 0.5 cm) were prepared and fill with the samples and indicator (bromphenol blue). The
electrophoresis was run in a refrigerator at 4oC for 3 h at 100 V at the beginning and increase to
200V.

Staining and visualization
After electrophoresis the gels were sliced producing three replicas that were placed in
different enzyme staining solutions. Gels were placed on a white light transilluminator to improve
the identification of bands colocalizing with the specific enzyme activities.

Data Analysis
The polymorphic bands were transformed into numeric data as co-dominant data, and run
by using POPGENE software (Yeh et all, 1999). The genetic variation intra and inter population
were measure with assumption population at HardyWeinbergs equilibrium, p2+2pq+q2 = 1.
Genetic variation (Ht) in a population was measure by Neis (1978), while genetic variation inter
population (genetic diferentiation=Gst) was measure as fixation index (Fst) of (Wright 1978); Gst =
Fst = (Ht-Hs)/Ht.


There were four alleles found with the various distributions. The common two allele was A
and B which express at the all isozymes. Four alleles were found at the EST, three alleles at the
ADH, ACP, MDH, and two alleles at PER and AAT (Table 1). Among the four alleles, A was the
th
most frequent in EST, ADH, and ACP, and express more than 50% (dominant). The allele C was
only found at EST with the lowest frequency (0.06) and categorized as a rare allele. Allele O
express in EST, ADH, ACP and MDH in low frequency (below 0,3).

Table 1. Allele frequency from total populations

Allele \ Locus EST PER ADH ACP MDH AAT
Allele A 0.5600 0.4400 0.8400 0.5600 0.3000 0.3800
Allele B 0.1400 0.5600 0.1600 0.1600 0.6600 0.3800
Allele C 0.0600 - - - - -
Allele O 0.2400 - 0.2800 0.0400 0.2400 -

Allele heterozygocity as shown at Table 2, was range from 0.2303 to 0.5631 with the mean
was 0.4197 (under 50%). The highest was at EST (0.5631), and the lowest was at ADH (0.2303).
The result express the low heterozygocity wich mean its low genetic diversity.

Table 2. Allele heterozygocity

Locus
Sample
size
Obs-Hom Obs-het Exp-hom* Exp Het* Nei** Ave Het
EST 50 0.6000 0.4000 0.3820 0.6180 0.6056 0.5631
PER 50 0.7600 0.2400 0.4971 0.5029 0.4928 0.3307
ADH 50 0.6800 0.3200 0.7257 0.2743 0.2688 0.2303
ACP 50 0.8400 0.1600 0.4057 0.5943 0.5824 0.4220
MDH 50 0.4800 0.5200 0.5176 0.4824 0.4728 0.4641
AAT 50 0.7200 0.2800 0.3331 0.6669 0.6536 0.5083
Mean 50 0.6800 0.3200 0.4769 0.5231 0.5127 0.4197
St. Dev 0.1265 0.1265 0.1405 0.1405 0.1377 0.1218
* Homozygocity and heterozygocity estimation (Levene ,1949)
**Number of polymorphic loci = 6; Proportion of polymorphic loci = 100.00 %

The genetic differentiation (Gst = Fst) as shown at Table 3, was very large, which
performed by the Fst = 1.1485. A very large genetic differentiation was performed by Fst more than
0.25.

Table 3. F statistic and gene flow estimation

Locus Sample size Fis Fit Fst Nm*
EST 50 0.2847 0.3339 0.0688 3.3863
PER 50 0.2581 0.5015 0.3280 0.5121
ADH 50 -0.4273 -0.1967 0.1616 1.2970
ACP 50 0.6161 0.7165 0.2617 0.7053
MDH 50 -0.1472 -0.1293 0.0156 15.7817
AAT 50 0.4444 0.5663 0.2194 0.8896
Mean 50 0.2268 0.3650 0.1788 1.1485
*Nm = Gene flow estimated from Fst = 0.25(1 - Fst)/Fst.

According to Wright (1978), genetic differentiation classified as follows:
Fst = 0 0,05 indicated low genetic diffrentiation
Fst = 0,05 0,15 indicated moderate genetic differentiation
Fst = 0,15 0,25 indicated large genetic differentiation
Fst > 0,25 indicated very large genetic differentiation
Gene flow (Nm) was estimated from genetic differentiation (Gst) as follow:
Nm = 0.5(1 - Gst)/Gst

th
A very large genetic differentiation, mean there were very large differentiation between
(inter) populations, and indicated low genetic diversity at intra populations. This is also indicated the
very low of gene flow. At this condition, conservation strategy was need to conserve of all
population, and sampling was need from representative of all population.

References

Ambasta S.P. 1986. The usefull plants of India. Publ. & Inform. Dir. Council of Scientific and Industrial Research.
New Delhi, India
Bourinbaiar AS; Lee-Huang, S. 1995. The non steroidal anti inflammatory drug, Indomethacin, as an inhibitor of
HIV replication. FEBS Letters 360 (1):85-88
Burkill IH. 2002. A dictionary of economic product of Malay Peninsula. Vol. 2. Ministry of Agriculture Malaysia,
Kuala Lumpur.
Goyder D. 2008. Hoya multiflora Blume. Curtis Bot. Magazine 7(1): 3-6.
Hoffman C, van Donkelaar R, Albers F. 2002. Hoya R.Br. In Albes F & Meve U (Eds.): Illustrated Handbook of
Succulent Plants: Asclepiadaceae. Berlin: Springer-Verlag. pp: 146 - 158
Kleijn D. and R van Donkelaar. 2001. Notes on The Taxonomy and ecology of the genus Hoya (Asclepiadaceae)
in Central Sulawesi. Blumea 46: 457 -483
Rahayu S. 2001. Genetic diversity of Hoya in Sumatra. [S2 thesis]. Bogor Agric. Univ. Bogor
Rahayu S, Sutrisno. 2007. Potency of Hoya seed in propagation and conservation: case study on Hoya
parasitica Wall. Buletin Kebun Raya10 (2) : 33-39 [Indonesian]
Rahayu S, Kusmana C, Abdulhadi R, Jusuf M, Suharsono. 2010. Distribution of Hoya multiflora Blume at
Gunung Gede Pangrango National Park, Indonesia. Journal of Forestry Research 7 (1): 42-52
Wanntorp L, Koycan A, Renner S. 2006. Wax plants disentangled: A phylogeny of Hoya (Marsdenieae,
Apocynaceae) inferred from nuclear and chloroplast DNA sequences. Molecular Phylogenetics and
Evolution 39: 722-733
Zachos E. 1998. Practical uses of various Hoya species. The Hoyan 19 (4)/20 (1): part II: 6-10/3-8
Soltis DE, Soltis PS. 1989. Isozymes in plant biology. Dioscorides Press, Portland, Oregon .
Zeidler M. 2000. Electrophoretic analysis of plant isozymes. Acta Univ. Palacki. Olomuc. BIOLOGICA 38 : 716
Yeh FC, Yang Rc , and Boyle T. 1999. POPGENE VERSION 1.31 Quick User guide. Univ of Alberta and
CIFOR. Canada

th
th
Endophytic Bacteria as an Alternative Agent for the Biological Control
of Plant Parasitic Nematodes on Black Pepper

Abdul Munif
a,*
, Rita Harni, Siswanto
b

a
Department of Plant Protection, Bogor Agricultural University ,Bogor, Indonesia
b
Research and Development Agency, Ministry of Agriculture, Indonesia
*Corresponding author: Department of Plant Protection, Bogor Agricultural University,
Jl. Kamper Kampus IPB Darmaga, Bogor, Indonesia 16680.
[email protected]

Abstract

Plant parasitic nematodes cause damage and losses significantly to black pepper in Indonesia. Control of plant
parasitic nematodes with pesticides is often restricted due to their high toxicity and negative impact on the
environment. The need for environmentally safe control strategies has increased interest in developing biological
control measures. Endophytic bacteria are ubiquitous in most plant species and reside within healthy plant
tissue without producing symptoms of damage. The internal plant habitat provides several advantages for
endophytic bacteria as biological control agents: 1) colonization of an ecological niche also used by plant
pathogens, 2) less competition with other microorganisms, 3) sufficient supply wirth nutrients, 4) less exposure
to environmental stress factors, and 5) better translocation of bacterial metabolites throughout the host plant.
The objective of this work was to evaluate the effect of endophytic bacteria isolated from black pepper to control
Meloidogyne incognita on black pepper. The results showed that some endophytic bacteria were able to reduce
the root galls caused by Meloidogyne incognita and juveniles of nematodes in the soil up to 70% as well as to
promote the growth of pepper seedlings.

Keywords: endophytic bacteria, Meloidogyne incognita, black pepper, root gall

Introduction

Black pepper (piper nigrum L) is one of the important export commodities in Indonesia.
However, the production of black pepper is now threatened by pests and diseases. One of the main
disease on black peper is yellow diseasae caused by plant parasitic nematodes i.e. Meloidogyne
sp. and Radopholus similis. Several control methods have been developed to combat the
nematodes, but they are still a serious problem of black pepper especially in Bangka Island,
Indonesia. The use of chemical pesticides with persistent pesticides can result in negative impacts
to the environment, pathogens become more resistant, disruptive presence of beneficial microbes in
the soil, and human health. Use of pesticides also provides residual effects on pepper which is
currently an one obstacle for consumers, mainly for export purposes that are very concerned about
the health and environmental aspects. In connection with the need to develop a system of
agricultural production, including plant disease control systems are environmentally sound one of
them by optimizing the use of biological agents.
Endopyitic bacteria are bacteria living inside plant tissues without doing symptoms on
these plants. As the internal plant habitat, endophytic bacteria provide several advantages as
biological control agents: 1) colonization of an ecological niche also used by plant pathogens, 2)
less competition with other microorganisms, 3) sufficient supply with nutrients, 4) less exposure to
environmental stress factors, and 5) better translocation of bacterial metabolites throughout the host
plant. Several studies have shown that endophytic bacteria isolated from various plant tissues are
able to suppress plant parasitic nematodes Meloidogyne incognita on cotton and tomato plants
(Hallmann 2001) as well as to control plant nematode Pratylenchus sp on patchouli (Harni 2010). In
addition, some bacterial isolates endophytes have been reported to enhance plant growth because
th
it can increase the availability of nutrients to induce plant resistance. The objective of this research
was to determine the potential of biological agents bacterial endophytes isolated from pepper for
controlling Meloidogyne incognita on pepper and their effects on the plant growth.


Isolation of Endophytic Bacteria
A total of 10 samples of healthy pepper plants were taken at random each of pepper
plants and were cultivated in Bangka, Bogor and Sukabumi. The pepper plant roots were
transported to the laboratory for immediate processing. The roots were washed with running tap
water to remove adherent soil particles then blotted dry on tissue paper. The root material was
weighed and surface sterilized with alcohol at 70% for 30 sec and in 2% of sodium hypochlorite
(NaOCl) containing 0.01% of Tween 20 for 3 min, followed by four rinses with sterile 0.01 M of
potassium phosphate buffer (PB) at pH of 7.0 (80 g NaCl, 2 g KCl, 11.5 g Na
2
HPO
4
, 2 g KH
2
PO
4
).
To confirm complete surface sterilization (sterility check), the surface disinfected roots were
imprinted on Tryptic Soy Agar (TSA). If bacterial growth occurred within 48 h, samples were
discarded. The pepper roots were then macerated with a sterile mortar and pistil in three times PB
(w/v). The macerate was decanted into sterile conical flasks and shaken for 30 sec. A dilution series
was made and 100 l of each dilution was plated onto 1/10 strength of TSA on petri disk. Petri
plates were incubated at 24C for 2-3 days and colony forming units (cfu) were determined. Three
replicates were made for each dilution. On each petri plate containing approximately 10 bacterial
strains was marked and all bacterial strains from this zone were transferred and purified on full
strength of TSA. The bacterial strains were stored in Tryptic Soy Broth (TSB) plus 20% of glycerol
at -20C. Two isolates collection of endophytic bacteria were used in this experiment.

Inoculum of Parasitic Nematodes
Inoculum of nematode Meloidogyne incognita was isolated from the infected roots pepper
of nematodes in Central Bangka, Province Bangka-Belitung Indonesia. Subsequently, the
nematodes were cultured and propagated on susceptible tomato plants (cv. Ratna) for 2 months.
After that plant was uprooted and the nematodes was extracted and used as a source of inoculum.

Effect of Endophytic Bacteria on Meloidogyne incognita
The effectiveness of biological agents against M. incognita on pepper seedlings was done
in a greenhouse. Two months pepper cuttings with one segment were treated with isolates of
endophytic bacteria. Eight isolates of selected bacterial endophytes isolated from root pepper and
patchouli isolate MER7, AA2, HEN1, HEN3, MER9, ANIC, TT2 and EH11 were used in this study.
The bacterial isolates were grown on TSA medium 100% for 24-48 h at room temperature. A single
colony of the bacterial isolate was transferred into 100 ml of liquid TSB medium and shaken for 2
days with a speed of 150 rpm at a room temperature. Furthermore, the bacterial suspension was
centrifuged at 11.000 rpm for 15 min at -4
o
C to separate the supernatant/culture filtrate with a
bacterial cell culture. Suspension of bacteria was made by diluted the bacterial cell with sterile
water. Roots of 3 months old of pepper seedlings were soaken for 1 h in bacterial suspension with a
population density of 10
9
-10
10
CFU. The treated pepper was planted subsequently in pots. One
week after the bacterial treatment, the plants were inoculated with 1000 larvae of the nematode M.
incognita per plant. Each treatment was repeated for 5 times and arranged in a completely
randomized design, with positive control was the plant only nematode inoculation, while negative
control was plants no inoculation with nematodes. Three months after inoculation the plants were
harvested and the number of galls and the population of nematodes in the roots and the soil were
observed as well as the plant height and weight, root weight, number of branches and number of
leaves.
th

Effect of Endophytic Bacteria against M. incognita on Black Pepper
In this study, eight isolates of endophytic bacteria isolated from root pepper and patchouli
were tested on seedling of black pepper against M. incognita in the greenhouse. All of isolates of
bacterial endophyte were able to reduce gall and juveniles of M. incognita. Four out of eight
isolates, i.e EH11, HEN1, HEN3 and TT2 significantly reduced gall nematodes compared to the
control. Isolate EH11 showed the highest in reducing gall nematodes compared to other isolates
(Table1). The isolates of bacteria were also able to suppress juveniles of nematode in the soil
compared to control. Six isolates of EH11, AA2, HEN1, MER9, ANIC and TT2 significantly reduced
number of juveniles compared to control. The highest influence in suppressing number of juveniles
of M.incognita was showed by isolate HEN1 and followed by EH11. Five Isolates of HEN1, EH11,
TT2, ANIC, and AA2 were able to reduce the population of M. incognita in the soil at more than
75%.

Table 1. Effect of isolates of biological agents bacterial endophyte against the number of galls and the
population of nematodes larvae

Treatments Number of
galls
Population of the
juveniles
Population of
reduction (%)
Isolate MER 7 70,4 ab 1212 b 15,36
Isolate EH11 9,0 c 23 ef 96.97
Isolate ANIC 66,0 ab 312 cde 78,21
Isolate MER 9 57,4 ab 504 c 64,80
Isolate AA2 48,8 bc 352 cd 75,41
Isolate HEN1 42,2 bc 13 f 99,00
Isolate HEN3 38,4 bc 1176 b 17,87
Isolate TT2 32,6 bc 50 ef 96,50
Control + (with nematode) 101,0 a 1432 ab -
Values followed by same small letters on the same column are not significantly different at 5% by DMRT.

Biological agents can suppress the development of plant diseases through a mechanism
of competition, predation and the resulting antibiotics (Kloepper et al. 1991). Some research
indicates that the use of biological agents endophytic bacteria through seed treatment reduce 30-
50% of the amount of gall of M. incognita on cotton plants (Hallmann et al. 1997). Some bacterial
endophytes isolated from the roots patchouli suppress populations of Pratylenchus brachyurus at
73.9% on patchouli plants in the greenhouse (Harni et al. 2007). Biological agents, including
endophytic microbial may protect plants against plant-parasitic nematodes through various ways
such as by producing toxic compounds that are nematicidals (Sikora et al. 2007; Yang et al. 2011).
In addition, certain bacteria can also suppress the development of plant diseases due to the ability
of bacterial endophytes in binding Fe (III) and to produce HCN (Keel et al. 1992). A treatment of
culture filtrate of endophytic bacterial isolate isolated from patchouli was also able to reduce
Pratylenchus barchyurus larvae up to 100%, 24 h after the treatment (Harni 2007).
Application of several bacterial endophytes can increase plant growth of black pepper.
Isolate MER7 increased plant hight of pepper, number of branches and number of leaves (Table 2).
Isolates EH11, MER9, TT2 increased plant height compared to control, while isolate HEN1
increased the number of brances compared to control. Vetrivelkalai et al. (2010) reported that
bacterial endophytes suppressed the gall number of nematodes on bhendi, but not all of bacterial
isolates increased the plant growth.

th
Table 2. The influence of endophytic bacteria on the growth of pepper plants inoculated with M. incognita 3
months after treatment

Treatments
Plant height addition
(cm)
Numbers of
branches increment
Numbers of
leaves increment
Isolat MER7 24,20 a 4,6 a 12,6 ab
Isolat EH11 21,60 ab 2,0 bcd 9,4 abc
Isolat MER9 20,40 ab 2,0 bcd 10,0 abc
Isolat TT2 20,40 ab 1,6 bcd 7,8 bc
Isolat AA2 18,80 ab 2,0 bcd 7,8 bc
Isolat HEN1 17,60 ab 2,8 abc 9,2 abc
Isolat HEN3 16,40 ab 2,2 bcd 9,2 abc
Isolat ANIC 14,76 b 1,2 cd 5,2 c
Control + (with nematode) 16,00 b 0,4 d 6,4 c
Values followed by same small letters on the same column are not significantly different at 5% Duncan test.

Inoculation with nematodes caused damage from the stabbing stylet and secretion of
enzymes released nematodes when the nematodes feed. Hallmann et al. (1997) reported that
nematodes are taking root cells can reduce the ability of plants to absorb water and nutrients from
the soil and cause symptoms such as lack of water and nutrients. Besides, the reduced
concentration of plant growth regulators such as auxins, cytokinins and gibberellins can occur
because the nematode secretes enzymes cellulose and pectinase that may degrade the cell up to
the root tip injuries and broken, this leads to auxin is not active then growth of plant will be stunted.

Acknowledgements

The authors would like to thank the leader of the program at the Secretariat of Research and
Development. The research was made possible with the support of funding from the State Budget of Research
and Development Agency, Ministry of Agriculture.

References

Hallmann J, Quadt-Hallmann A, Mahaffee WF, Kloepper JW. 1997. Bacterial endophytes in agricultural crops.
Canadian Journal of Microbiology 43:895-914
Hallmann J, Quadt-Hallmann A, Miller WG, Sikora RA, Lindow SE. 2001. Endophytic colonization of plant by
biocontrol agent Rhizobium etli G12 in relation to Meloidogyne incognita infection. Pyhtopathology
91:415-422
Harni R, Munif A, Supramana, Mustika I. 2007. Pemanfaatan bakteri endofit untuk mengendalikan nematode
peluka akar (Pratylenchus brachyurus) pada tanaman nilam. Jurnal Hayati 14 (1): 7-12.
Keel C, Schneider U, Maurhofer M, Voisard C, Laville J, Burger U, Withner P, Hass D, Defago G. 1992.
Suppression of root disease by Pseudomonas fluorescens CHAO: Importance of the bacterial secondary
metabolite 2,4 diacetylphloroglucinol. Mol. Plant-Microbe Interaction 5:4-13.
Kloepper JW, Zablotowiz RM, Tipping EM, Lifshiftz R. 1991. Plant growth promoting mediated by bacterial
rhizosphere colonizers. In: Keister DL and Cregan PB.(Eds.). The Rhizosphere and Plant Growth.
Kluwer Academic Publisher. Dordrecht, The Netherland. P:315-326.
Sikora RA, Schafer K, and Dababat AA. 2007. Modes of action associated with microbially induced in planta
suppression of plant parasitic nematodes. Australasian Plant Pathol. 36:124-134.
Vetrivelkalai P, Sivakumar M, Jonathan FI. 2010. Biocontrol potential of endophytic bacteria on Meloidogyne
incognita and its effect on plant growth in bhendi. Journal of Biopesticides 3 (2): 452-457
Yang CJ, Zhang XG, Shi GY, Zhao HY, Chen L, Tao K, Hou TP. 2011. Isolation and Identification of endophytic
bacterium W4 against tomato Botrytis cinerea and antagonistic activity stability. African Journal of
Microbiol. Res. 5 (2): 131-136.
th
The Effect of Organic and Inorganic Fertilizers on Growth and Yield
of Red Ginger (Zingiber officinale Rosc.)

Rudiyanto* and Tri Muji Ermayanti

Research Center For Biotechnology LIPI
Jl. Raya Bogor Km. 46 Cibinong Bogor 16911, Indonesia
Phone: +62-21-8754587, Fax: +62-21-8754588

Abstract

Ginger (Zingiber officinale Rosc.) has been used for medicinal purposes in Southeast Asia since ancient times.
Yield of ginger is affected by soil where the crop grows, climatic conditions and its cultivation management.
Similar to other tuber crops, ginger needs high nutrients on soil. The objective of this experiment was to
investigate the growth and yield of red ginger plants grown in media suplemented with organic and inorganic
fertilizers. The research was conducted in a glasshouse in the Research Center for Biotechnology LIPI. The
treatments tested were factorial between the medium and fertilizers used, with the total of treatments was 16
with 5 replicates of each treatment. Treatment M1 was soil : manure : grit (1:1:1); M2 was soil : manure : chaff
(1:1:1); M3 was soil : manure : grit (1:2:1); M4 was soil : manure : chaff (1: 2:1); P0 was no addition of fertilizer
control treatment); P1 was NPK granule (18:9:10) at 5 g/plant; P2 was NPK (20:20:20) at 1 g/l given once a
week; P3 was NPK (32:10:10) at 1 g/lt giving once a week. Growth and yield parameters measured were height,
number of leaves, number of shoots, stem diameter (from 0 to 24 weeks), leaves fresh and dry weight, stem
fresh and dry weight, root fresh and dry weight, and leaf area recorded at month 4 and 6. After 9 months, red
ginger was harvested to determine its yield. The results indicated that treatment with M2P2 was the best
treatment for height, number of leaves and stem diameter, of red ginger, meanwhile M4P3 resulted in the
highest number of shoots among the others (11.25). The highest production of rhizome of red ginger plant after
9 month growth was achieved by M1P2 treatment (174.058 gr fresh weight/ polybag and 19.75 dry weight/
polybag). Physiological parameters showed that the highest Leaf Area Index (LAI) value was from M2P2
treatment (3.83 after 4 months of growth), and from M4P3 (6.415448, after 6 month of growth); M3P2 treatment
produced the highest net assimilation rate (NAR) at 0.01, M3P1 had the crop growth rate (CGR) value at
0.031548. The best value of Harvest index (HI) was reached by M3P0 treatment at 2.038.

Keywords :Zingiber officinale Rosc., red ginger, organic and inorganic fertilizers, growth, yield

Introduction

Ginger (Zingiber officinale Rosc.), a monocotyledon belonging to family Zingiberaceae and
in the natural order Scitamineae, is herbaceous perennial, usually grown as annually for its pungent
rhizome. It is native of Southeast Asia and one of the earliest oriental spices known to Europe
(Parthasarathy et al., 2003; Ravindran and Babu, 2005; Kandiannan et al., 2009). Ginger normally
propagates by its rhizome. Ginger has been used for medicine purposes in Asia since the ancient
times. For example, it is used as folk medicine, as a carminative, stimulant of the gastro-intestinal
tract, and counter-irritant. The rhizome is believed to have diaphoretic and diuretic effects, and anti-
inflammatory. Extracted ginger rhizome contains gingerol inhibits the growth of Helicobacter pylori
CagA+ strains in vitro, and may contribute to chemopreventative effects (Mahady et al., 2003).
Ginger is also widely used as a spice in forms of fresh ginger, dried whole or powdered ginger, and
preserved ginger.
Crop yields is a function of three major factors; namely the soil where the crop is grown,
climatic conditions and management practices. Like other root and tuber crops, ginger has a high
th
nutrient demand on soils. It does well in farmlands newly opened from long fallows, making use of
nutrients reserves accumulated during the fallow period (Attoe et al., 2009)
Management practices used in agriculture will influence soil properties, nutrient use
efficiency and crop production. Conventional crop management systems that rely on inorganic
fertilizers and agrochemicals have, in recent years, increased agricultural productivity, albeit at a
high environmental cost (Pimentel, 2005). Organic farming systems which depends on organic
sources of nutrients (i.e., animal manure, crop residues, green manure crops and catch crops) may
sustain productivity at reduced environmental cost by enhancing microbial nutrient turnover
(Watson et al., 2002).
The objective of our study was to investigate the growth and yield of red ginger plants
grown in media suplemented with organic compared with inorganic fertilizers.


The research was conducted in a glasshouse in the Research Center for Biotechnology
LIPI. The treatments tested were factorial between the medium and fertilizers used, with the total of
treatments was 16 with 5 replicates of each treatment. Table 1 showed the combination treatment
of inorganic and organic fertilizers used in this experiment.

Table 1. Treatment of Combination between organic and inorganic fertilizer

Code P0 P1 P2 P3
M1 M1P0 M1P1 M1P2 M1P3
Note: M1: soil : manure : grit (1:1:1) M2: soil : manure : chaff (1:1:1)
M3: soil : manure : grit (1:2:1) M4: soil : manure : chaff (1: 2:1)
P0: no addition of fertilizer (control treatment) P1: NPK granule (Decastar 18:9:10) at 5 g/plant
P2: NPK (Hyponex 20:20:20) at 1 g/l given once a week P3: NPK (Growmore 32:10:10) at 1 g/l giving once a week

Seedlings of 1 month old were used in this experiments. Seedlings were grown in
polybags of 25 x 30 cm. Each polybag contained growth medium with different trreatment of
fertilizers as shown at Table 1. Growth and yield parameters measured were height, number of
leaves, number of shoots, stem diameter recorded from 0 to 24 weeks. However, since the data
were plenty, only data at week 24 was presented. After 9 months, red ginger was harvested to
determine its yield as fresh and dry weight of the rhizomes.


Growth of red ginger after 24 weeks planting on different combinations of fertilizer types
and concentratitons was shown at Table 2. The results indicated that treatment with M2P2 was the
best treatment for height, number of leaves and stem diameter, of red ginger (Table 2), meanwhile
M4P3 resulted the highest number of shoots among other treatments. This indicated that the best
medium for growing red ginger until 24 weeks was a combination between M2; soil: manure: chaff
(1:1:1) and NPK fertilizer containing NPK (20:20:20) at 1 g/l that was given once a week.
Unlike the case with other treatments, Slow Release fertilizer (P1: NPK granule (18:9:10)
at 5 g/plant) actually had no significant effect on shoot growth performance, which were indicated
by the low values of plant height, leaves number, shoots number and the plant diameter. Ginger is
an herbaceous plant that needs nutrient appropriately. When it was fertilized with the low supply of
nutrients from the granular fertilizer, the optimum vegetative growth could not be achieved.
th
Nutrient management is always an important consideration for ginger since large quantities
of nutrients is required for optimal growth, especially for N, P and K nutrients. However, farmers
generally overuse N, P and K and ignore manure fertilization. They are not used to apply
appropriate fertilization in many crops, therefore they need knowledge about balanced fertilization
between inorganic and organic fertilization (Li et al., 2010). Organic and conventional farming
practices differ in the use of several agriculture management strategies, including the use of cover
crops, green manure, and fertilization, which may influence soil properties, greenhouse gas
emissions and productivity of agroecosystems.

Table 2. Growth of red ginger after 24 weeks of planting treated with different combinations of fertilizer type and
concentration

Treatment code* Height of plant (cm) Number of leaves Number of shoots Stem diameter (cm)
M1P0 70.33 36.00 5.67 0.50
M1P1 54.07 42.00 4.33 0.37
M1P2 82.38 94.75 9.00 0.58
M1P3 74.83 63.75 6.00 0.48
M2P0 82.33 50.33 5.33 0.50
M2P1 99.13 111.00 10.00 0.55
M2P2 100.63 104.25 9.00 0.63
M2P3 80.025 99.00 9.50 0.55
M3P0 79.23 66.67 7.33 0.57
M3P1 34.00 18.00 4.00 0.30
M3P2 75.63 53.00 6.75 0.48
M3P3 63.38 42.75 7.50 0.48
M4P0 81.83 84.00 8.00 0.57
M4P1 82.13 98.25 9.50 0.63
M4P2 94.50 116.25 9.00 0.63
M4P3 93.25 123.50 11.25 0.53
Note : *description of each code of treatment is shown at Table 1.

Note : each code of treatment is presented on Table 1.

Figure 1.Leaf Area Index (LAI) of red gingeron 4 (A) and 6 month (B) of age.

Leaves are important organs of the plant. Leaf area (LA) is a variable key for most
agronomic and physiological studies involving plant growth, light interception, photosynthetic
efficiency, evaporation, and responses to fertilizers and irrigation (Blanco & Folegatti, 2005).
Therefore, LA strongly influences growth and productivity. Estimating LA is a fundamental
component of crop growth models (Lizaso et al., 2003). Figure 1 showed that the M4P2 treatment to

0
0.5
1
1.5
2
2.5
3
3.5
4
4.5
M
1
P
0
M
1
P
1
M
1
P
2
M
1
P
3
M
2
P
0
M
2
P
1
M
2
P
2
M
2
P
3
M
3
P
0
M
3
P
1
M
3
P
2
M
3
P
3
M
4
P
0
M
4
P
1
M
4
P
2
M
4
P
3
L
e
a
f

A
r
e
a

I
n
d
e
x
s

Treatment

0
1
2
3
4
5
6
7
M
1
P
0
M
1
P
1
M
1
P
2
M
1
P
3
M
2
P
0
M
2
P
1
M
2
P
2
M
2
P
3
M
3
P
0
M
3
P
1
M
3
P
2
M
3
P
3
M
4
P
0
M
4
P
1
M
4
P
2
M
4
P
3
L
e
a
f

A
r
e
a

I
n
d
e
x
s

Treatment B A
th
ginger resulted the highest value of leaf area index (LAI) at 4 months after planting. However, at 6
month old plant, the highest LAI was achieved when treated by M4P3 treatment combination.
The perennial rhizome of the ginger plant is a specialized segmented stem structure that
grows horizontally just under the soil surface. Upright-growing shoots are produced from the tips of
lateral rhizome branches. Adventitious roots and lateral growing points emerge from the nodes of
the rhizome stem. In ginger, the roots emerge from the lower rhizome sections. For commercial
purposes, ginger is grown as an annual crop, the rhizomes are harvested after seven to nine
months when the rhizome is physiologically ripened (Wilson &Ovid, 1993).

A

B

Note : each code of treatment is presented on Table 1.

Figure 2. Fresh weight (A) and Dry Weight (B) of red ginger rhizomes after 9 months old grown on various
fertilizer application.

Figure 2 showed that the highest fresh and dry weight of rhizomes produced by treatment
M1P2. M1 was soil: manure: grit (1:1:1) medium with the addition of NPK fertilizer supplement
(Hyponex 20:20:20) at 1g/l given once a week (P2). While the lowest weight of rhizomes was
produced on the M3P1 treatment, where M3 was soil: manure: grit (1:2:1) medium and P1 was a
slow release NPK granules (with N:P:K ratio of 18:9:10) with the dose of 5 g/plant. This result
indicated that the slow release fertilizer (P1) provided less amount of nutrient than what ginger plant
required during the maximum vegetative growth and generative phase.
Ginger plants, that was grown in soil containing more manures increased ginger plant
growth and rhizome production. The use of humic acid as a fertilizer could directly affect
physiological processes in plants. Besides its role as an auxin, humic acids directly influence the
0
20
40
60
80
100
120
140
160
180
200
M
1
P
0
M
1
P
1
M
1
P
2
M
1
P
3
M
2
P
0
M
2
P
1
M
2
P
2
M
2
P
3
M
3
P
0
M
3
P
1
M
3
P
2
M
3
P
3
M
4
P
0
M
4
P
1
M
4
P
2
M
4
P
3
F
r
e
s
h

W
e
i
g
h
t

(
g
r
a
m
)

Treatment
0
5
10
15
20
25
M
1
P
0
M
1
P
1
M
1
P
2
M
1
P
3
M
2
P
0
M
2
P
1
M
2
P
2
M
2
P
3
M
3
P
0
M
3
P
1
M
3
P
2
M
3
P
3
M
4
P
0
M
4
P
1
M
4
P
2
M
4
P
3
D
r
y

W
e
i
g
h
t

(
g
r
a
m
)

Treatment
th
metabolic processes of plants such as respiration, synthesis of nucleic acids, and ion absorption.
The highest rhizome production of red ginger plant after 9 month growth was achieved by M1P2
treatment (174.058 gr fresh weight/ polybag and 19.75 dry weight/ polybag). In addition to that, the
best value of Harvest index (2.038) was reached by M3P0 treatment.

References

Attoe E.E. and Osodeke V.E. 2009. Effects of NPK on Growth and Yield of Ginger (Zingiber Officinale Roscoe)
in Soils of Contrasting Parent Materials of Cross River State. EJEAFChe, 8 (11): 1261-1268
Blanco, F.F., Folegatti, M.V. 2005. Estimation of leaf area for greenhouse cucumber by linear measurements
under salinity and grafting. Sci. Agric. 62, 305309.
Kandiannan, K., Parthasarathy U., Krishnamurthy K.S., Thankamani C.K., Srinivasan V. 2009. Modeling
individual leaf area of ginger (Zingiber officinale Roscoe) using leaf length and width. Scientia
Horticulturae 120: 532537
Lizaso, J.I., Batchelor, W.D., Westgate, M.E. 2003. A leaf area model to simulatecultivar-specific expansion and
senescence of maize leaves. Field Crops Res. (80) 117.
Li L., F. Chen, D. Yao, J. Wang, N. Ding, and X. Liu. 2010. Balanced Fertilization for Ginger Production. Better
Crops Vol. 94; No. 1: 25-27
Pimentel, D. 2005. Environmental and economic costs of the application of pesticides primarily in the United
States. Environ. Develop. Sustain. 7, 229252.
Watson, C.A., Atkinson, D., Gosling, P., Jackson, L.R., Rayns, F.W. 2002.Managing soil fertility in organic
farming systems.Soil Use Manage. 18, 239247.
Wilson, H. & Ovid, A. 1993. Growth and yield responses of ginger (Zingiber officinale Roscoe) as affected by
shade and fertilizer applications. J. Plant Nutrition 16(8):1539-1545.

th
Growth Analysis of Superior Clones of
Temulawak (Curcuma xanthorrhiza Roxb.) Grown with Organic Fertilizers

Bambang Pujiasmanto* and Samanhudi

Department of Agrotechnology, Faculty of Agriculture, Sebelas Maret University
Jl. Ir. Sutami 36A, Surakarta, Indonesia 57126
* Corresponding author: Tel./Fax: +62 271 637457;
[email protected]

Abstract

Curcuma xanthorrhiza as a medicinal plant needs to be preserved and improved for its yield. The curcumin is
very useful for human health. This species is useful to improve the body immune system. Curcumin of many
genotypes of C. xanthorrhiza has been successfully evaluated for their potentials and its potential yield from
genotypes throughout Java and islands for selection of superior clones. The research was done based on the
Randomized Completely Block Design (RCBD), using superior clone types as the single factor obtained from
Sragen, Jember, Sumenep, Pasuruan, Blitar, and Malang. The data were analyzed using F-test at significance
level of 5% followed by Duncan Multiple Range Test (DMRT) at significance level of 5%. The results showed
that Malang clone had the best vegetative growth and maximum yield compared with other clones. The plant
height, leaves number, leaf width, leave area, leaf area index (LAI), dry weight of straw, fresh rhizome weight
variables of Malang clone was the highes among other clones. The maximum vegetative growth pattern of plant
height obtained by Malang clone that reached 155.13 cm, the highest fresh rhizome production of Malang clone
was 22.31 tons/ha.

Keywords: growth analysis, temulawak, Curcuma xanthorrhiza, organic fertilizer

Introduction

Temulawak (Curcuma xanthorrhiza Roxb.) is one species of medicinal plants belonging to
family Zingiberaceae is potential to be developed, and is one of nine types of seed plants from the
Directorate General of POM as an ingredient. Utilization of this plant is varied. It is useful for
maintenance and improvement of health and treatment of disease as well as raw materials for
traditional medicines and cosmetics (Nurjannah et al., 1994). Temulawak rhizome can be used as
hepatoprotector, increase the body's immune system, anti-bacterial, anti-diabetic, anti-hepatotoxic,
anti-inflammatory, anti-oxidant, anti-tumor, diuretic, depressant, hipolipodemik, and as beverage as
well as for natural dyes (Purnomowati and Yoganingrum, 1997; Raharjo and Rostiana, 2006).
All potentials should be evaluated to determine the type of temulawak with the most
potential to be developed in certain areas. Several types of temulawak has been successfully
evaluated its potential based on curcumin content and gowth characteristics for selection of all
types of temulawak throughout Java. Kuswanto has been elected six best types of temulawak,
including Sragen, Pasuruan, Blitar, Sumenep, Malang, and Jember.
Temulawak selected cultivars need to be tested in various production areas, in order to
investigate their genetic capabilities grown in various areas. One of the evaluation was done by
planting selected temulawak, the superior clones was then elected to be cultivated at the production
centers of temulawak in the district of Sragen, Central Java.

th

This study was started in May 2010, at Karang Pong, Kali Jambe, Sragen, Cetral Java,
located at 7 30' LS and 110 50' BT and altitude of 180 m above sea level. The soil type is vertisol.
The materials used in this study were temulawak seeds, consisting of six clones derived from the
superior selection of Java.
The design of the experiment was Randomized Completely Block Design (RCBD). Origin
of clones was used as the single factor. The experiment had 6 standard of excellence e.i. 6 clones
obtained from Java. Each treaatment had 3 replicates. Addition of organic fertilizer was of 15
tons/ha manure.
Observation variables included plant height, number of leaves per clump, number of tillers
per hill, leaf width, leaf area, leaf area index, fresh weight of rhizomes per plant, dry weight of straw,
specific leaf area, and relative growth rate. Data were analyzed using the F test at 5% level, if there
was a significant difference, then it was followed by DMRT at the level of 5%.


Height of Plant
Malang clone temulawak observed at intervals of two weeks showed high growth rate of
plants significant different compared with other clones (Figure 1). Malang clone growth at 5 WAP
seemed to have the fastest plant height compared with five other clones. This shows the level of
adaptation of Malang clone was very high, especially during the process of adding plant height.

Figure 1. Plant height of six superior clones of temulawak (Curcuma xanthorrhiza).

Table 1. The average plant height of six superior clones of temulawak (Curcuma xanthorriza) at 19 WAP

Clones
Plant height (cm)
I II III
Total Average
Sragen
108.80 98.13 99.50
306.43
102.13 c
Jember
68.38 60.63 68.25
197.26
65.75 ab
Sumenep
45.00 59.38 53.75
158.13
52.71 a
Pasuruan
67.75 69.25 87.75
224.75
74.92 b
Blitar
86.50 61.75 61.25
209.50
69.83 ab
Malang 151.00 146.60 167.80 465.40 155.13 d
Note: Values followed by the same letter showed no significantly difference according to DMRT at 5%.

Increased plant height of Malang clone during vegetative growth was the highest among
the clones. Sragen clone was the second having the plant height similar to Malang clone. At the late
th
vegetative phase (19 WAP) height of Sragen clone was only 102.13 cm, which was much lower
than that of Malang clone (155.13 cm) (Table 1). This would indicate that vertisol soil type is
suitable for temulawak. Plant height among the clones was significantly different at 5% with Malang
clone was the best.

Number of Leaves and Number of Tillers per Clumps
The number of leaves of the temulawak represents its during the vegetative phase. When
the plants reach the generative phase, the existing leaves turns to dry. The increased of leaf
number may also indicate the increase of rhozome production of temulawak. The more number of
leaves formed, the better rhizome formation during the vegetative phase of the plants. The number
of leaves produced by temulawak tuber is influenced by the number of tillers formed in a single
clump of plants. The leaves formed by the temulawak having a lot of puppies will increase the
number of leaves corresponded to the number of puppies available. Tillers per clump of temulawak
are capable of producing 6-9 leaves which affects the increasing number of leaves in one plant.
Statistical analysis that there was no significant different among clones of temulawak in
terms of leaf number. Figure 2A shows that the highest number of leaves found on the Malang
clone, while the Sumenep clone produced the lowest of number of leaves. The number of tillers per
hill shows that the Pasuruan and Malang clones had the highest number of tillers (Fig. 2B) the
average number of tillers per hill reached 3.17. However, this amount was not significantly different
with other clones

A B

Figure 2. Number of leaves (A) and of six clones of temulawak (Curcuma xanthorrhiza) at 19 WAP.

Pasuruan clones into clone with the highest number of suckers, is due to the number of
seedlings have buds more when compared with the five other clones. This will impact on the growth
of temulawak, number of shoots that emerged after the primary buds more so it appears as a leafy
plant with a number of seedlings in a clump of more than one. The number of chicks that many of
the temulawak will have a negative effect form of competition for the acquisition of nutrients and
light. For the competition in terms of food reserves during early growth, the number of chicks that
more will tend to have stronger competition because it has only one rhizome pieces that serve as
the seed.

Leaf Width, Leaf Area and Leaf Area Index
Leaf width of all clones were not significantly difference (Figure 3A), and there was no
difference on their leaf morphology. The width of the leaf ranged from 10.96 cm to 18.00 cm. The
leaf area was significantly difference among the clones with the Malang clones was the best.
Malang clones had the highest leaf area with an area of 1,008.83 cm2, while for the lowest on
Sumenep clones with only 244.55 cm
2
leaf area (Figure 3B). The leaf area index is related to
photosynthetic ability of plants. Widiastuti et al., (2004) reported that at low light intensity plants
produce larger leaves, thinner with a thin layer of epidermis. It has slight palisade tissue, wider
th
spaces between cells, and more number of stomata. Meanwhile, plants that received high-light
intensity produces smaller leaves, thick, compact with fewer number of stomata, the cuticle layer
and a thicker cell wall with space between cells is smaller and hard texture of leaves.

A B C

Figure 3. Leaf width (A), leaf area (B) and leaf area index (C) of six clones of temulawak (Curcuma xanthorrhiza)
at 19 WAP.

Greater leaf area may be harmful, it can also be beneficial to plants. Large leaf area would
be advantageous for plants because it will enhance the ongoing process of photosynthesis. Optimal
photosynthesis caused photosynthesis product formed also increased, so plant growth will be
optimal. Irwanto (2009) revealed that the products of photosynthesis are proportional to the total
active leaf area that can perform photosynthesis. Widiastuti et al. (2004) reported that with
increased leaf area, assimilates generated will also be greater. Narrow leaf area beneficial for
plants because it can reduce water loss through excessive transpiration.
Leaf area index obtained after the analysis was performed to Malang clone has a real
difference when compared with leaf area index of the other five clones. Temulawak was obtained
from leaf area index is not too large. Of the six clones of temulawak only five clones are at rates
below one. Malang clones became the most extensive high-leaf area index reached 1.13 (Figure
3C). This shows that for the Malang clones had interaction especially among the leaves of shade
plants. Meanwhile, other five clones had a smaller leaf area index, which was about 0.5. No
interactions occur among the clones because of wide spacing used in the experiment was higher
than the leaf area produced of temulawak.
The higher of leaf area index (LAI) was beneficial. Sitompul and Guritno (1995) reveal that
the density of the leaves is closely related populations of plants or plant spacing. The closer the
distance between plants, the higher the density between the leaves and fewer quanta of radiation
(light) is to layers of lower leaves.

Biomass Dry Weight and Fresh Rhizome Weight per Plant
The statistical analysis showed that Malang clone had the highest biomass production
significantly different with other clones (Figure 4A). Dry weight of Malang clones was 168.1 g, the
lowest was Pasuruan clone having 27.55 g. This indicated that with increasing leaf area of
temulawak was total plant dry weight increase corresponded to the crop yields increase.
When leaf area was higher then its dry weight, this will correspond directly to the total dry
weight of the plants. Similarly, the weight of rhizomes that produced was also high. High weight of
biomasss showed that the assimilation process may also rearchs to maximum.
Statistical analysis of rhizome fresh weight showed that there was significantly difference
among the clones. Malang clone obtained the highest rhizome fresh weight per plant (422.57 g)
(Figure 4B), meanwhile Pasuruan clones was the lowest, only reached 105.49 g. Conversion into
yield per hectare Malang clones was 22.31 tons. Other temulawak clones was reported to have less
th
then 20 tons per hectare. Therefore, Malang clone was potential to be promoted as the best clone.
This clone is best when it grows intensively on the vertisol soil.

A B

Figure 4. Dry weight of biomass (A) and rhizome fresh weight (B) of six clones of temulawak (Curcuma
xanthorrhiza) at 19 WAP

Specific Leaf Area
Specific leaf area of six different clones showed no significantly different when they were
observed until 17-23 WAP. At 17 WAP, Pasuruan was the best, significantly different compared with
other clones, but only Sragen clone was significantly different compared with Sumenep clone at 23
WAP (Table 2).

Table 2. Specific leaf area of temulawak (cm
2
)

Clones
Age (WAP)
17 19 21 23
Sragen
4,033.3 a 3,136.7 a 8,143.3 a 8,033.3 b
Jember
3,806.7 a 1,930.0 a 3,760.0 a 2,710.0 ab
Sumenep
2,556.7 a 886.7 a 1,620.0 a 1,556.7 a
Pasuruan
9,533.3 b 7,083.3 a 24,360.0 a 6,656.7 ab
Blitar
4,033.3 a 1,736.7 b 1,780.0 a 1,993.7 ab
Malang
4,526.7 a 2,863.3 a 4,150.0 a 3,336.7 ab
Note: Numbers followed by same letter on the same column are not significant at different levels of multiple range tests of
Duncan's 5%.

Relative Growth Rate (RGR)
RGR on almost all clones of temulawak at the age of 19-21 weeks after planting tend to
reduce. The high reduction occurred when plants were 21 weeks old, except for Pasuruan and
Blitar clones lowest RGR occurred at the age of 23 weeks after planting (Table 3). This occurs
because the plant entered generative phase. After entering the generative phase of growth, clones
Malang, Jember, Sumenep, and Sragen increased in RGR. This showed that the clones were ble to
produce a new dry matter per unit at initial dry material. Meanwhile, Pasuruan and Blitar clones was
not able to produce new dry matter per unit at initial dry material.
Table 3 shows that clones of temulawak from Malang has the highest RGR than the other
clones both at the beginning of growth or to close to maximum vegetative growth.
Decline in RGR indicated the differences in rates of photosynthesis. The process of
photosynthesis will be disrupted if water is not enough to plants. A low rate of photosynthesis may
decrease to growth of vegetative organs, especially to the plant height. The decrease in
photosynthesis may be due to increase of stomata diffusion and non-stomata barrier. Decrease of
th
RGR may also due to the slow growth of vegetative organs (leaf area, plant height, number of
tillers, dry weight, and root dry weight of plants).

Table 3. Relative growth rate (RGR) of temulawak (g/week)

Clones
Age (WAP)
19 21 23
Sragen
2.17 ab 1.37 a 1.40 a
Jember
2.40 ab 1.52 ab 1.61 ab
Sumenep
2.46 ab 1.60 ab 1.68 b
Pasuruan
1.75 a 1.77 ab 1.65 b
Blitar
2.09 ab 1.78 ab 1.55 ab
Malang
2.83 b 2.21 b 2.44 c

Note: Numbers followed by same letter on the same column are not significant at different levels of multiple range test of
Duncan's 5%.

Conclusions

Malang superior clone had the maximum vegetative growth and yield of its fresh rhizome.
This clone also had the highest of the plant height, leaf number, leaf width, leaf area, leaf area index
(LAI), dry weight of straw, rhizome fresh weight, specific leaf area, and RGR. The maximum plant
height of Malang clone was 155.13 cm, the fresh rhizomes of temulawak was 22.31 tons/ha.

References

Irwanto. 2010. Effect of shade on growth differences Shorea sp. in nurseries.
http://www.geocities.com/irwantoforester/naungan_shorea.pdf. Accessed, May 27, 2010.
Nurjannah N, S Yuliani, AB Sembiring. 1994. Temulawak (Curcuma xanthorrhiza). Review of Outcomes
Research. Research Institute for Spices and Medicinal Plants. X (2): 43-57.
Purnomowati S and A Yoganingrum. 1997. Temulawak (Curcuma xanthorhiza Roxb.). Center for documentation
and information science, LIPI, Jakarta. 44p.
Rahardjo M and O Rostiana. 2006. Cultivation of Rare Medicinal Plants of Purwoceng (Pimpinella pruatjan
Molkenb). Proceedings of the National Seminar and Exhibition of Medicinal Plant Development towards
Independence Family Medicine Society in Jakarta on September 7. P. 138-146.
Sitompul SM and B Guritno. 1995. Plant Growth Analysis. Gadjah Mada University Press. Yogyakarta.
Widiastuti L, Tohari, and E Sulistyaningsih. 2004. Effect of light intensity and levels dominosida on microclimate
and plant growth in pot chrysanthemum. Agrivita 11 (2) :35-42.

th
th
Effect of Drought and Inoculation of Arbuscular Mycorrhizal Fungi in
Enhancing Productivity and Tolerance Mechanism of Grasses

PDMH Karti,
a*
L Abdullah
a
, J Nulik
b
, Nurhayati
c
, OR Nahak
d
, S Nofyangtri
a

a
Faculty of Animal Science, Bogor Agricultural University, Bogor, West Java. Indonesia
b
BPTP, Naibonat, Kupang,NTT, Indonesia
c
BPT, Ciawi, West Java, Indonesia
d
University of Timor, NTT, Indonesia
*
Corresponding author:

Faculty of Animal Science, Bogor Agricultural University,
Bogor, West Java. Indonesia.
Hp :+6281314227713
[email protected]

Abstract

Drought stress considered to be one of the most important limiting abiotic factors of plant growth and yield in
many areas, and Arbuscula Mycorrhizal Fungi (AMF) symbiosis can protect host plants against its detrimental
effect. This research was conducted to study the effect of drought and inoculation of Arbuscula Mycorrhizal
Fungi on the productivity and tolerance mechanisms of Stenotaphrum secundatum and Ischaemum timurensis
grasses. This research used a completely randomized design with four treatments: D
0
(Control), D
1
(with AMF),
D
2
(drought), and D
3
(drought and with AMF). Parameters observed were the soil moisture content, leaf water
potential, leaf relative water content, shoot and root dry weight, root length, proline, and soluble sugar. The data
were analyzed with analysis of variance (ANOVA) and the differences between treatments were analyzed with
Duncan range test. The results showed that drought stress significantly (P<0.05) decreased soil water content,
leaf water potential, leaf relative water content, shoot dry weight in Stenotaphrum secundatum. Drought stress
significantly (P<0.05) decreased soil water content and leaf water potential, but enhanced proline and soluble
sugar content in Ischaemum timurensis. AMF inoculation did not affect productivity of Stenotaphrum
secundatum, but in Ischaemum timurensis enhanced proline and soluble sugar content but decreased leaf water
potential on drought stress. One of the tolerance mechanism in Ischaemum timuriensis is by increasing the
proline and soluble sugar contents.

Keywords: drought, arbuscular mycorrhizal fungi, grasses, Stenotaphrum secundatum, Ischaemum timurensis

Introduction

Plants in nature are continuously exposed to several biotic and abiotic stresses, water
deprivation being one of the commonest. Soils too dry for crop production have been estimated to
cover 28% of the earth's land surface (Bray, 2004). Nevertheless, plants have developed several
physiological, biochemical, and molecular mechanisms in order to cope with drought stress.
Besides the natural responses of plants against drought, it must be considered that most terrestrial
plants can establish a symbiotic association with the arbuscular mycorrhizal fungi (AMF). When the
AMF symbiosis is established the fungus receives carbon molecules from the plants, and the plants
receive nutrients (especially phosphorus) and water from the fungus (Harrison, 2005; Gosling et al.,
2006). In this way, AM plants are usually more tolerant to several stresses, including drought, than
non-AM plants (Aug, 2001, 2004; Ruiz-Lozano, 2003; Ruiz-Lozano et al., 2006). This research
was conducted to study the effect of drought and inoculation of AMF to the productivity and
tolerance mechanisms of Stenotaphrum secundatum and Ischaemum timurensis Grasses

th

The materials used in this study were two types of grasses namely Stenotaphrum
secundatum, and Ischaemum timurensis. The two types of grasses are the result of selection about
30 forage species on preliminary research (Karti, 2010). Other materials used were fiber pots as
many as 32 units (diameter = 20, high = 100 cm), Mycofer, growing media in the form of soil and
manure, tools WP4 potentiometer, coolbox, and others.
This research used a completely randomized design with four treatments: D
0
(control), D
1

(with AMF), D
2
(drought), and D
3
(drought and with AMF) and four replications. Parameters
observed were soil moisture content, leaf water potential, leaf relative water content, shoot and
root dry weight, root length, proline (Bates, 1973), and soluble sugar (Dubois et al., 1956 modified
by Buysse & Merckx, 1993). The data were analyzed with analysis of variance (ANOVA) and the
differences between treatments were analyzed with Duncan range test.


Drought stress significantly (P<0.05) decreased soil water content, leaf water potential,
leaf relative water content, shoot dry weight in Stenotaphrum secundatum (Table 1). AMF without
drought treatment did not show significant differences, but it showed significant different (P<0.05)
in drought treatment. Drought stress reduced levels of the soil led to a decrease in water
absorption. The low uptake of water caused the shoot dry weight decreased because of declining
photosynthesis process. The addition of AMF increased significantly (P<0.05) the shoot dry weight,
this is due to the ability of AMF in increasing absorption of water so that improving the
photosynthesis process.

Table 1. Effect of drought and the addition of AMF to soil moisture, leaf water content, relative water content,
shoot dry weight, and root dry weight of Stenotaphrum secundatum

Variables
Treatments
Do D1 D2 D3
Soil moisture 38.45 0.46 a 39.14 0.59 a 23.76 1.04 b 22.98 0.79 b
Leaf water potential (-Mpa)
-0.68 0.2 b -0.51 0.6 b -6.79 1.6 a -7.00 1.7 a
Relatif water content (%) 82.28 2.8 a 87.2 6.4 a 29.69 6.4 b 34.51 10.2 b
Shoot dry weight (g/pot)
27.6 3.5 a 29.0 4.7 a 14.7 2.1 c 22.3 2.3 ab
Root dry weight (g/pot)
2.5 1.9 4.8 3.5 2.9 0.7 3.2 1.0
Description: D
0
(control), D
1
(with AMF), D
2
(drought), and D
3
(drought and with AMF).

Table 2. Effect of drought and the addition of AMF to soil moisture, leaf water potential, leaf relative water
content, root length, shoot dry weight, and root dry weight, proline and soluble sugar of Ischaemum
timuriensis

Variables
Treatments
Do D1 D2 D3
Soil moisture (%) 35,52 0,58
a
35,33 1,97
a
23,15 1,28
b
24,32 2,01
b

Leaf water potential (-Mpa) -1,02 0,19
b
-1,36 0,11
a
-1,46 0,17
a
-1,19 0,27
ab

Leaf relative water content (%) 88,25 3,50
a
88,48 0,90 86,10 1,71 86,78 0,72
Root lenght (cm) 128,0 6,38 128,50 5,80 128,25 4,92 127,75 11,76
Shoot dry weight (g/pot) 38,87 9,21 41,70 18,36 29,10 12,35 30,70 5,88
Root dry weight (g/pot) 5,30 3,77 6,65 4,20 8,30 3,76 10,23 2,99
Proline 51,68 7,63
H
43,36 7,04
H
67,48 7,43
H
59,05 17,73
H

Soluble sugar 6,64 2,43
LM
4,78 1,36
M
23,09 2,71
EF
17,24 1,88
GH

Description: D
0
(control), D
1
(with AMF), D
2
(drought), and D
3
(drought and with AMF)

th
In Ischaemum timuriensis drought stress significantly (P<0.05) decreased the soil moisture
content, leaf water potential, and significantly increased (P<0.05) the proline and dissolved sugar,
but did not show significant effect in leaf relative water content, root and shoot dry weight. In
drought conditions, plants decreased leaf water potential, but with the addition of AMF the decrease
could be minimized compared to that with non-AMF. In these plants, drought treatment did not
cause a change in relative leaf water content, root and shoot dry weight. This suggests that these
plants include drought resistant crops. Tolerant plants that can increase levels of proline and
soluble sugar to maintain water absorption so that the growth process can run well.
Drought resistance mechanisms in Ischaemum timuriensis is by secreting proline and
soluble sugar. In Figure 1 shows that drought stress increased proline levels in both treatments with
the addition of AMF or not. In Ischaemum timuriensis a sharp increase in proline was seen after
40
th
day.

Figure 1. Proline Content of Ischaemum timuriensis.
In Ischaemum timuriensis (Figure 2) shows that drought stress showed the highest
elevated levels of dissolved sugar. The addition of AMF on drought stress decreased levels of
dissolved sugar, it means that the AMF can increase the absorption of water through the hyphae.

Figure 2. Soluble Sugar of Ischaemum timuriensis.

Conclusion

Drought stress can reduce soil moisture, leaf water potential, leaf relative water content,
shoot dry weight in Stenotaphrum secundatum. AMF inoculation on drought stress can increase the
shoot dry weight. On Ischaemum timuriensis drought stress can reduce soil moisture, leaf water
potential, and increasing proline and sugar dissolved. Ischaemum timuriensis is included in drought-
resistant plants with resistance mechanisms through the increased secretion of proline and soluble
sugar.
th
References

Aug, RM. 2001, Water relations, drought and vesiculararbuscular mycorrhizal symbiosis. Mycorrhiza. 11:3-42.
Auge. RM. 2004. Arbuscular mycorrhizae and soil/plant water relations. Canadian Journal of Soil
Science.84:373-381.
Bates LS. 1973. Rapid determination of free proline for water-stress studies. J Plant and Soil 39:205207.
Buysse J, R Merckx. 1993. An improved colorimetric method to quantify sugar content of plant tissue. J
Experimental Botany 44:16271629.
Bray, EA. 1997. Plant responses to water deficit. Trends in Plant Science. 2:48-54.
Dubois M, KA Gilles, JK Hamilton, PA Rebers, F Smith. 1956. Colorimetric method for determination of sugars
and related substrances. Anal. Chem. 28:350356.
Gosling, P, Hodge, A, Goodlass G, Bending GD. 2006. Arbuscular mycorrhizal fungi and organic farming.
Agriculture, Ecosystems and Environment.113:17-35.
Harrison M.J. 2005. Signaling in the arbuscular mycorrhizal symbiosis. Annual Review of Microbiology. 59:19-
42.
Karti PDMH. 2010. Development of drought resistant grasses and legumes through a quick selection techniques
and efficient management of aquaculture. The conference of the Research result. Research institutions
and community empowerment. Bogor Agricultural University.
Ruiz-Lozano, J.M. 2003, Arbuscular mycorrhizal symbiosis and alleviation of osmotic stress. New perspectives
for molecular studies. Mycorrhiza . 13:309-317.
Ruiz-Lozano, J.M., Porcel R., Aroca, R. 2006. Does the enhanced tolerance of arbuscular mycorrhizal plants to
water deficit involve modulation of drought-induced plant genes. New Phytologist. 171:693-698.

th
The Cooling Effect of Forage Crop, Kudzu (Pueraria lobata) Vine Covering
over Livestock Buildings

Takuya Koyama
a
, Mika Yoshinaga
b
, Kei-ichiro Maeda
a
and Akira Yamauchi
a*

a
Department of Biosphere Resources Science, Nagoya University, Nagoya, Japan
b
Department of Architecture, Meijo University, Nagoya, Japan
*
Corresponding author: Nagoya University, Chikusa, Nagoya 464-8601, Japan
[email protected]

Abstract

Heat stress during summer season can decrease livestock productivity, and cause high economic losses to
livestock farmers. Although many cooling techniques (e.g. sprinklers, fans, etc.) are available to improve the
thermal environment of livestock buildings, they require high construction and energy costs. This research aims
to investigate an economical livestock buildings covering method with kudzu (Pueraria lobata), which can be
used as a cooling technique during summer season and as forage for livestock after use. Kudzu is a fast-
growing, climbing and perennial vine, and its shoot can be utilized as high nutritious feed for livestock. In this
study, the cooling effect of the covering method with kudzu was investigated by comparing the room
temperatures (RTs) between the covered (Covered) and the non-covered fabricated house (height 2.6 m, width
3.65 m, depth 1.83 m) (Non-covered). Two-year-old kudzu seedlings were transplanted beside the south side of
the houses in May 2009 and 2010 and induced to climb the plastic nets placed over the south walls and roofs of
the houses. RTs of Covered and Non-covered and global solar radiation were measured every 5 minutes during
summer season in 2009. The covering rate and the leaf number in 18 frames (0.4 m 0.4 m each) that were set
on the south wall and roof of Covered and stem length were measured every 2 weeks in 2009. The covering rate
and the dry weight in 120 frames were measured during autumn 2010. The stem length reached around 4 m
long by July 2009. In general, the height of a standard livestock building is around 4 m. These facts showed that
two-year-old kudzu seedlings could cover the walls of a standard livestock building during summer season. The
estimated average covering rate and leaf number among 18 frames, and the RT differences between Covered
and Non-covered showed positively significant relationships (P<.001). The maximum RT difference was
observed to be 3.44 C, when the estimated average covering rate was 43.9 % and the estimated average leaf
number was 529 leaves m-2. The covering rate and dry weight in the frame showed a positively significant
relationship (P<.001). The maximum dry weight of 253.4 g m-2 was observed when the covering rate was
80.8%. We conclude that the kudzu covering is an effective cooling technique for livestock buildings during
summer season and is potentially capable of producing biomass to provide feed for livestock after use.

Keywords: kudzu, green wall, heat stress, livestock productivity, forage crop.

Introduction

The global average surface warming in the 21st century will range from 1.1 to 6.4 C
(IPCC, 2007). The global warming has the potential to occur adverse thermal conditions in the
livestock building, which can ultimately reduce productive performance or possibly cause deaths of
livestock (Hahn, 1995). Thus, some techniques for environmental modifications such as water
misting with spray, forced ventilation with fans or air-conditioning, shading with insulated roof or
reflective coated roof are needed to maintain animal production (West, 2003). On the other hand,
the employment of these techniques causes higher energy consumption, worsens global warming,
and increases general costs for animal production (Nardone, 2010).
The ultimate goal of this study was to establish the economical livestock buildings covering
method with the use of kudzu (Pueraria lobata (Willd.) Ohwi) vine. That is to cover the walls and
roofs of livestock buildings with kudzu vine, which can be used as a cooling technique during
summer seasons and as feed for livestock after use.
th
Kudzu is a fast-growing, climbing and perennial vine. Their vines can grow 10 to 30 m in
one growing season (up to 30 cm a day), and create broad canopies (Mitich, 2000). Farmers in the
USA cultivated kudzu over a terrace to provide shade in the early 1900s (Tsugawa, 1986).
Moreover, kudzu has the wide range of utilization as forage because it is able to provide feed for
sheep, swine and chickens as well as cattle (Kristen, 2011). Chemical composition and digestibility
characteristics of kudzu were equivalent to other commonly fed forage (Corley et al., 1997)
The use of external vegetation can be a useful tool for thermal regulation for buildings.
Holm (1989) showed using dynamic computer model that the leaf cover produces a constant 5 C
cooling effect in room temperature in summer. The vegetation consistently lowered the wall surface
temperature by about 17 C, and saved air-conditioning energy as high as 80% (Meier, 1990).
However, these studies placed little or no emphasis on the conditions of the plants.
Ip et al. (2010) analyzed the shading performance of a vertical climbing plant canopy by
measuring number of leaf layers, area of canopy with each leaf layer and solar transmissivity, and
established the thermal model that enables to present the shading performance of the climbing
plant canopy over its annual growing and wilting cycle. Unlike non-biological devices, the conditions
of plant sare affected by not only the characteristics of plants such as leaf area, leaf number, leaf
thickness, leaf angle, leaf movement and moisture content of leaves but also the response to the
environmental conditions such as solar radiation, ambient temperature, humidity and soil moisture
content, which affect the shading performance, the thermal insulation and evaporative cooling
produced by transpiration.
The objectives of this paper were to investigate the cooling effect of the dynamic changes
of kudzu vine covering by comparing the room temperatures (RTs) between the covered (Covered)
and the non-covered container house (Non-covered), and to evaluate the dry matter production of
kudzu vine that was used for the economical livestock buildings covering method. The leaf number
and covering rate in each frame that was set on the south wall and roof of Covered, the room
temperatures of Covered and Non-covered, and environmental conditions around the houses were
determined at regular intervals during summer season. At harvest, the covering rate and dry matter
weight in 120 frames were measured.


Plant materials
Hard-stems (lignified) were collected from kudzu natural stands in the Graduate School of
Bioagricultural Sciences, Nagoya University (3509N, 13558E) from April to May in 2008 and
2009. Then, the hard-stems were cut into around 12 cm with one node and grown in the commercial
and artificial soil that is well-drained and poorly nutrient in plastic container (585mm long, 185mm
wide and 145mm deep). After cuttings were rooted and sprouted, they were transplanted to plastic
pots (25 cm in diameter and 30 cm in height) containing air-dried paddy soil and raised in a
glasshouse for one year. In winter 2008 and 2009, all stems were cut at 5cm from the soil surface,
and afterwards left undisturbed. Next spring, some buds were sprouted from the rooted cuttings.
Sprouted nursery stocks (plant materials) were only used for this study.

Experimental design
Four container houses (2600mm high, 3650mm wide and 1830mm long) were set in series
from east to west on the Togo field of the Graduate School of Bioagricultural Sciences, Nagoya
University (3506N, 13704E) in 2009, and 5 container houses were set in 2010. One container
house excluding both ends was not covered with kudzu vine (Non-covered), and plant materials
were transplanted beside the other container houses in May 25, 2009 and May 24, 2010, and
induced to climb the plastic nets (mesh size: 120mm120mm) placed on the south wall and the roof
of the houses.
th
Measurements
Only two container houses excluding both ends (Non-covered and Covered) were used for
evaluating the effect of the dynamic changes of kudzu vine covering on the room temperature
reduction in 2009. The houses on both ends were excluded because they received more solar
radiation than the inner houses. The stem length, the leaf number and covering rate in each frame
(400mm400mm), which was set on different heights of the south wall (650mm, 1300mm and
1950mm above the soil surface) and on different locations of the roof (465mm, 915mm and
1365mm from the south edge of the roof), were measured on the 3 plants except both ends every 2
weeks from June 10 to September 29, 2009.The estimated average leaf number and covering rate
among 18 frames were calculated from the inclination of averages of these data.The room
temperatures (RTs) of Covered and Non-covered were recorded every 5 minutes with thermo
recorder (TR-72U: AD Co. LTD.) and global solar radiation was recorded every 5 minutes with
pyranometer (MS-801: EKO INSTRUMENT CO., LTD.) from July 15 to September 22, 2009.To
evaluate the dry matter production of the economical livestock buildings covering method with use
of kudzu vine, the covering rate and the dry weight in 120 frames, which were located on the south
wall and the roof of 4 containers, were measured during autumn in 2010.

Image analysis
Before taking digital images of Covered, the white-colored frames (400mm400mm) were
set behind the plants and in front of the south walls and roofs to facilitate processing images. Digital
images, composed of 12 megapixel, were obtained with the digital camera (-7040: OLYMPUS
corporation). The backgrounds except the plants in the frames were cleared manually, and plants
were converted into binary image with photoshop (Adobe Photoshop CS2: Adobe). The pixels of the
processed image were calculated with imageJ (Public domain software for image processing and
analysis in Java). Calculated pixels of the plants and the frames were used for computing the
covering rate.

Results and discussion

The stem length reached around 4 m long by July, and some vines exceeded 10 m at the
end of August in 2009. In general, the height of a standard livestock building is around 4 m. These
facts showed that two-year-old kudzu seedlings could cover the walls of a standard livestock
building during summer season.
Fig. 2 shows that the changes in estimated average leaf number and covering rate among
18 frames. The estimated average leaf number gradually increased until the middle of July in 2009.
Afterwards, the estimated average leaf number increased rapidly and reached the peak of 530
leaves m-2 on September 10, 2009.The estimated average covering rate showed similar trend with
the estimated average leaf number, and it peaked at 45% at the final measurement on September
25.
The RTs of Non-covered were clearly influenced by ambient temperature and global solar
radiation. The RT differences between Non-covered and Covered were also influenced by ambient
temperature and global solar radiation. At the same time, the RT differences tended to gradually
increase. Therefore, the data of the RT differences were sorted and averaged out daily according to
the global solar radiation; every 0.2 kWM-2; and the processed data were used to highlight the
effect of the covering method with kudzu.
Under the global solar radiation conditions less than 0.2 kW m-2, there was a significantly
negative relationship between the RT differences, and the estimated average leaf number (P<.001)
and the estimated average covering rate (P<.001). However under the global solar radiation
conditions between 0.2 kW m-2 and 1.0 kW m-2, there were significantly positive relationships
between the RT differences, and the estimated average leaf number (P<.001) and the estimated
th
average covering rate (P<.001). The inclinations of each regression equations increased as the
global solar radiation increased under the global solar radiation conditions between 0.2 kW m-2 and
1.0 kW m-2. The maximum RT difference was observed to be 3.44 C, when the estimated average
covering rate was 43.9 % and the estimated average leaf number was 529 leaves m-2. The
covering rate and dry matter weight in the frame showed a positively significant relationship
(P<.001). The maximum dry weight of 253.4 g m-2 was observed when the covering rate was
80.8%.
We conclude that the kudzu covering is a possible cooling technique for livestock buildings
during summer season and is potentially capable of producing biomass to provide feed for livestock
after use.

This photo was taken on September 18, 2009.

Figure 1. Two container houses(2600mm high, 3650mm wide and 1830mm long) excluding houses on both
ends (Non-covered and Covered) were used for evaluating the effect of the dynamic changes of
kudzu vine covering on the room temperature reduction in 2009.

The estimated average leaf number and covering rate were calculated from the inclination of averages of leaf number and
covering rate among18 frames (400mm400mm), which were located on the south wall and roof of Covered.

Figure 2. Changes in the estimated average leaf number and covering rate among 18 frames in 2009.

References

Corley, R. N., Woldeghebriel, A. and Murphy, M. R. 1997. Evaluation of the nutriative value of kudzu
(Puerarialobata) as a feed for ruminants. Anim. Feed Sci. Technol. 68: 183-188
Hahn, G.L.1995. Environmental management for improved livestock performance, health and well-being. Jpn. J.
Livest. Management, 30(3): 113-127.
th
Holm, D. 1989.Thermal improvement by means of leaf-cover on external walls a simulation model. Energ.
Build. 14:1930.
Ip, K., Lam, M., Miller, A. 2010. Shading performance of a vertical deciduous climbing plant canopy. Build.
Environ. 45: 8188
IPCC (The Intergovernmental Panel on Climate Change).2007. Climate change 2007: Synthesis Report
2007..Geneva, Switzerland. Pp52.
Kristen, H. 2011. KUDZU. Am. Hist. 46 (2): 38-44
Meier, A. K. 1990.Strategic landscaping and air-conditioning savings: a literature review. Energ. Build. 15
16:479486.
Mitich, L. W. 2000. Intriguing world of weeds - Kudzu (Pueraria lobata (Willd.) Ohwi). Weed tech. 14: 231-235
Nardone, A., Ronchi, B., Lacetera, N., Ranieri, M.S., Bernabucci, U. 2010.Effects of climate changes on animal
production and sustainability of livestock systems. Livest.Sci.130: 57-69.
Tsugawa, H. 1986a. Cultivation and utilization of kudzu-vine (Pueraria lobata OHWI) taxonomy, geographical
distribution, use, breeding and propagation. J. Japan.Grassl. Sci.31(4): 435-443.
West, J.W. 2003. Effects of heat stress on production in dairy cattle.J. DairySci. 86: 2131 2144.

th
Effect of Weed Control Management on Herbage Yield and Quality
in the Established Dwarf Napiergrass (Pennisetum purpureum Schumach)

Renny Fatmyah Utamy
a
, Yasuyuki Ishii
b,
*, Sachiko Idota
b
, Lizah Khairani
c

a
Interdisciplinary Graduate School of Agriculture and Engineering, University of Miyazaki, Japan
b
Faculty of Agriculture, University of Miyazaki, Miyazaki, Japan
c
Graduate School of Agriculture, University of Miyazaki, Miyazaki, Japan
*Corresponding author: Faculty of Agriculture, University of Miyazaki, 1-1 Gakuen-kibanadai Nishi,
Miyazaki 889-2192, Japan. Tel.: +81 985 58 7251; fax: +81 985 58 7251.
[email protected]

Abstract

In our previous extension activity of dwarf variety of late-heading type (DL) napiergrass (Pennisetum purpureum
Schumach) to southern Kyushu, weed control management is found to be a crucial factor for obtaining good
establishment and considerable herbage dry matter (DM) yield in an established year. The objective of this study
was to examine the effect of several weed control practices, i.e. mixed sowing of annual setaria (abbreviated as
S), which has no regrowth ability in stem-elongated tillers, paper-mulching (as P) and hand-weeding (as W),
compared with no-weeding (as W) on DM yield and quality of this species for two years (Trial-1,2). Weed
control practices had a significantly (P < 0.05) positive effect on plant height, tiller density, percentage of leaf
blade and leaf area index in DL napiergrass, compared with no-weeding (S-W or W), and paper-mulching (P or
P+S-W) had the highest yields in both trials. Setaria-sowing had a partially mitigating effect of weed damage on
growth of DL napiergrass, while additive DM gain from setaria could compensate the yield decrease in DL
napiergrass and reduce herbicide cost. Neither IVDMD nor CP content was affected by any weed control in
either trial. Thus, paper-mulching and annual setaria-sowing could be a good proposal in weed control of this
species.

Key words: annual setaria, dwarf napiergrass, herbage yield, paper mulch, weed control

Introduction

Based on extension activity of dwarf variety of late-heading type (DL) napiergrass
(Pennisetum purpureum Schumach) to southern Kyushu, weed control management is found to be
a crucial factor to obtain good establishment of this grass and achieve considerable herbage yield in
the established year (Utamy et al., 2011). Hand-weeding was a sole weed control practice, which
caused physical and spiritual burden for farmers before the launch of herbicides. Therefore,
invention of easy and environmentally effective weed control technology has been strongly desired.
Weed invasion into the established forage crop fields is a visible sign of management
problems. Damages to forage crop production by weeds are mediated principally from loss in
growth rate and yield, and secondarily from decline in forage quality. However, in forage crop
production, use of herbicide should be avoidable because of the negative effect on livestocks and
increase in production cost (Sakai & Kawanabe, 1981).
Weeds in the inter-row space of DL napiergrass are normally controlled by hand-mowing
machine 23 times before the first defoliation of this grass. Repeated weed control is essential until
the leaf canopy is well established at the establishment. Even though close spacing is desirable
from the weed control point of view, weeds do invade even at 50 50 cm of plant spacing.
Mulching at the inter- and intra-row spaces reduces weed problems by preventing the seed
germination and suppressing growth of emerged weed seedlings, resulting in facilitating soil fertility
and plant productivity (Wilson et al., 1987; Obiefuna, 1991; Salau et al., 1992). Mulching is a well-
known method for the establishment of horticulture crop such as lettuce (Moniruzzaman, 2006) and
th
tomato (Anzalone et al., 2010) and also in paddy rice field (Won et al., 2011). In the grass
cultivation, mulching is often used as living mulch or cover crop such as white clover (Deguchi et al.,
2005), legume (Hiltbrunner et al., 2007) and hairy vetch (Mohammadi, 2010). However, paper-
mulching has not been applied to DL napiergrass as weed control management.
The other way for weed control management is the oversowing of annual grass species to
compete weed at the early growth of perennial forage crops. DL napiergrass was oversown with
temperate Italian ryegrass (Lolium multiflorum Lam.) to get herbage in the spring-early summer
season (Ishii et al., 2005). In the present study, tropical annual setaria (Setaria italica cv.
Natsukanso), released from Yukijirushi Seed Co. Ltd., is utilized as once-cutting herbage with no
regrowth ability if it starts stem elongation at the harvest, gives early summer growth, and should be
also ideal to suppress summer weeds at the early growth of perennial forage species (Wakamatsu,
2004).
Therefore, the objectives of this study was to examine the effect of weed control
management on dry matter yield and herbage quality in the established DL napiergrass by paper-
mulching, oversowing of annual setaria and several time of weeding practices, compared with no
weeding control in two years.


In 2008, DL napiergrass transplanted at 2 plants m
-2
was imposed by three treatments (P,
S+W, S-W) with three replications by Latin square design in Sumiyoshi Livestock Science Station
(3198N, 13146E), University of Miyazaki (Trial-1). In 2010, DL napiergrass transplanted at 2
plants m
-2
was imposed by four treatments (P+S-W, S+W, S-W, -W) with three replications by a
randomized block design in Kibana Agricultural Science Station (3183N, 13141E), University of
Miyazaki (Trial-2). Growth attributes including yield, in vitro DM digestibility (IVDMD) and crude
protein (CP) content as herbage quality were determined in both trials. Efficiency of weed control
practices in plant parameters, such DM yield, IVDMD and CP content, was evaluated by the
percentage of plant parameter value in each weed control practice to that in no weed control.


Weed control management had significantly (P < 0.05) positive effects on plant density,
tiller density, percentage of leaf blade and leaf area index in DL napiergrass, compared with no-
weeding (S-W or W), and paper-mulching (P or P+S-W) had the highest yields in both trials
(Figure 1).
Adoption of several weeding practices such as weeding, paper-mulching and setaria-
sowing can be assessed by the percentage of gain or loss in attributes under the particular practice
relative to those under no adoption of the practice (Table 1). Adoption of paper-mulching facilitated
to obtain largest positive gain of DM yield in DL napiergrass at two defoliations in both Trials 1 and
2, respectively. Situation was similar for the positive gain by adoption of hand-weeding, while the
degree of gain was reduced from paper-mulching (Table 1). The advantage of paper-mulching in
DM yield was closely corresponded with positive gain in plant height, tiller density and leaf area
index through improvement in light penetration (Peltzer & Kchy, 2001) and prevention of plant
damage from weeds (TruGreen Tree and Shurub Field Guide, 2008). Positive effect of paper-
mulching on DM yield matched with several crops such as paddy rice (Won et al., 2011), lettuce
(Moniruzzaman, 2006), tomato (Anzalone et al., 2010) and turmeric (Sanyal & Dhar, 2006).
Weed control management by sowing setaria had no significant (P > 0.05) effect to
suppress weed DM yield in Trial-2 (data not shown). However, 1 g m
-
DM production from setaria
reduced 4 g m
-
of DM production from weeds (y = 104.553 0.247x, r = 0.52, P > 0.05). In several
th
stand establishments of perennial species, annual species are used to suppress weeds and
mitigate the competition of crops from weeds. In the present study, annual setaria has
characteristics to give good growth in early summer and suppress summer weeds (Wakamatsu,
2004).

ns
ns
0
20
40
60
80
100
120
140
1 Jul 1 Aug 1 Sep 1 Oct 1 Nov 1 Dec
P
l
a
n
t

h
e
i
g
h
t

(
c
m
)
Date
P-W S+W S-W
(A) 2008
a
b
c
a
a
1st
2nd
b
0
20
40
60
80
100
120
140
P
l
a
n
t

h
e
i
g
h
t

(
c
m
)
Date
P+S-W S+W S-W -W
(B) 2010 a
a
b
b
a
a
ab
b
1st
a
a
a
b
a
b
c
c
2nd
0
30
60
90
120
150
T
i
l
l
e
r

(
N
o
.

m
-
2
)
Date
P+S-W S+W S-W -W
(D) 2010
a
a
b
b
a
1st
a
b
b
a
b
c
c
2nd
b
b
b b
ns
ns
0
30
60
90
120
150
T
i
l
l
e
r

(
N
o
.

m
-
2
)
Date
P-W S+W S-W
(C) 2008
a
1st
2nd
b
a
a
b
c

Arrows indicate the time for the first (1st) and second (2nd) defoliation. P, interrow space was covered by paper mulch; S,
oversown with setaria; W, weeding and W, no weed control. Symbols with different letters are significantly different among
weed control managements at each date by LSD method at 5% level. ns: P > 0.05.

Figure 1. Changes in plant height and tiller density of DL napiergrass under several weed control management
in 2008 (Trial-1) and 2010 (Trial-2).

Neither IVDMD nor CP content was affected by any weed control in either trial.
Consistently positive effect of any weed control practice on quality attributes was hardly obtained in
either trial, while decline in CP content under weeding and paper-mulching practices was common
at the second and first defoliation in Trial 1 and 2, respectively (Table 1). Living mulch with white
clover improved plant nutrition by enhancing phosphorus uptake in maize (Deguchi et al., 2005).
The present paper-mulching and hand-weeding could not contribute to herbage quality of DL
napiergrass, possibly due to the negative correlation of DM yield with quality attributes under similar
fertilization in this species. Dwarf napiergrass cv. Mott, which has almost equivalent plant attributes
to DL napiergrass, had IVDMD and CP content at 67.5 and 13.2%, respectively (Sollenburger et al.,
1988), almost corresponded with the present IVDMD at 74 and 60% at the first and second
defoliation, respectively, in Trial 1.
th

Table 1. Effect of weed control practices on efficiency in several parameters of plant total in DL napiergrass
at each defoliation in 2008 and 2010

Year Defoliation Parameter
Practice
Weeding Paper-mulching Setaria-sowing
2008 1st DM Yield 248 2466
(Trial 1) IVDMD 4 1
CP content 2 -9
2nd DM Yield 7554 54091
IVDMD 14 -6
CP content -16 -24
2010 1st DM Yield 74 275 -4
(Trial 2) IVDMD 6 7 1
CP content -19 -6 11
2nd DM Yield 73 73 36
IVDMD -1 -1 0
CP content -3 9 3

DM yield, dry matter yield; IVDMD, in vitro dry matter digestibility; CP content, crude protein content.

Conclusion

Paper mulch is not common to use in DL napiergrass cultivation, while it proved to be
effective to avoid weed damage and facilitate good growth with high DM yield of this species. Cost
of paper mulch is 50 yen/meter (Sanyo Seishi Co. Ltd., Tottori) and setting of paper mulch is a
labor-extensive weed control practice. Thus, based on the amount of natural seed bank of weeds,
paper mulch or other degradable mulching material can be applied to DL napiergrass, so as to
reduce weed competition at the establishment. Annual setaria-sowing gave advantage to get
herbage yield at the first defoliation of DL napiergrass, although prompt harvest time of annual
setaria should be examined in the mixed cropping with DL napiergrass.

References

Anzalone A, A Cirujeda, J Aibar, G Pardo, C Zaragoza. 2010. Effect of biodegradable mulch materials on weed
control in processing tomatoes. Weed Tech. 24: 369377.
Deguchi S, S Uozumi, T Tawaraya, H Kawamoto, O Tanaka. 2005. Living mulch with white clover improves
phosphorus nutrition of maize of early growth stage. Soil Sci. & Plant Nutr. 51: 573576.
Hilltbrunner J, P Jeanneret, M Liedgens, P Stamp, B Streit. 2007. Response of weed communities to legume
living mulches in winter wheat. Agron. & Crop Sci. 193: 93102.
Ishii Y, M Mukhtar, S Idota, K Fukuyama. 2005. Rotational grazing system for beef cows on DL napiergrass
pasture oversown with Italian ryegrass for 2 years after establishment. Grassl. Sci. 51: 223234.
Mohammadi GR. 2010. Weed control in irrigated corn by hairy vetch interseeded at different rates and times.
Weed Biol. & Manag. 10: 2532.
Moniruzzaman M. 2006. Effects of plant spacing and mulching on yield and profitability of lettuce (Lactuca sativa
L.). J. Agric & Rural Dev. 4: 107111.
Obiefuna JC. 1991. The effect of crop residue mulches on the yield and production pattern of plantain (Musa
AAB). Biol. Agric. & Hort. 8: 7180.
Peltzer DA, M Kchy. 2001. Competitive effects of grasses and woody plants in mixed-grass prairie. J. Ecol. 89:
519527.
Sakai H, S Kawanabe. 1981. Ecology of grassland weed in Japan. (In) Weeds and Weed Control in Asia. Aspac,
China. Pp. 216239.
th
Salau A, NOA Opara, R Swennen. 1992. Effect of mulching on soil properties, growth and yield of plantain on a
tropical utisol in southeastern Nigeria. Soil and Tillage Research. [home page on the Internet]. [cited on 17
January 2011]. Available from URL: http://www.sciencedirect.com/science?_ob=ArticleURL&_.
Sanyal D, P Dhar. 2006. Effect of mulching, nitrogen and potassium levels on growth, yield and quality of
turmeric grown in red lateritic soil. [home page on the Internet]. [cited on 13 January 2011]. Available from
URL: http://www.actahort.org/books/769/769_17.htm.
Sollenberger LE, GM Prine, WR Ocumpaugh, WW Hanna, CS Jones Jr, SC Schank, RS Kalmbacher. 1988.
Mott Dwarf Elephantgrass: A high quality forage for the subtropics and tropics. Circular S-356.
Agricultural Experiment Station, Institute of Food and Agricultural Sciences, University of Florida,
Gainsville, Florida, USA. Pp. 118.
TruGreen Tree and Shrub Field Guide. 2008. Tree/shrub fact sheet. [home page on the Internet]. [cited on 13
January 2011]. Available from URL:
http://info.trugreen.com/ci/fattach/get/141926/1274121076/session/L2F2LzEvc2lkL0lEM3gqUmpr.
Utamy RF, Y Ishii, S Idota, N Harada, K Fukuyama. 2011. Adaptability of dwarf napiergrass under cut-and-carry
and grazing systems for smallholder beef farmers in southern Kyushu, Japan. J. Warm Region. Soc. Anim.
Sci., Japan, 54: 6576.
Wakamatsu I. 2004. Yukijirushi Seed Co. Ltd. Bokusou to Engei. 52 (2): 1316. (In Japanese).
Wilson GF, R Swennen, E De Langhe. 1987. Effect of mulch and fertilizer on yield and longevity of a medium
and giant plantain and banana cultivars. Proceeding of the Third Meeting on International Cooperation for
Effective Plantain and Banana Research, 27-31 May 1985. IARPB/INIBAP. Abidjan, Cote dlvoire. Pp.
109111.
Won HY, JK Kim, WT Jeon, HS Han, JY Kim, JJ Shin. 2011. Paper Mulching Management for Weed Control
and Rice Growth in Paddy. [home page on the Internet]. [cited on 7 January 2011]. Available from URL:
http://a-c-s.confex.com.

th
Effect of Density of Mother Plants on Efficiency of Nursery Production in
Dwarf Napiergrass (Pennisetum purpureum Schumach)

Asuka Yamano
a
, Yasuyuki Ishii
b,
*, Koutarou Mori
a
, Renny F Utamy
c
, Sachiko Idota
b

a
Graduate School of Agriculture, University of Miyazaki, Miyazaki, Japan
b
Faculty of Agriculture, University of Miyazaki, Miyazaki, Japan
c
Interdisciplinary Graduate School of Agriculture and Engineering, University of Miyazaki, Japan
* Corresponding author: Faculty of Agriculture, University of Miyazaki, 1-1 Gakuen-Kibanadai Nishi,
Miyazaki 889-2192, Japan.
Tel.: +81 985 58 7251; fax: +81 985 58 7251.
[email protected]

Abstract

Recently, dwarf napiergrass (Pennisetum purpureum Schumach) of late-heading type (named as DL) was
introduced widely for multi-purpose uses into Kyushu Island, Japan. Napiergrass needs to be propagated
vegetatively, while nursery production was not efficiently established yet. We examined to obtain an optimal
plant density of mother plants for the efficient nursery production (per both unit land area and labor time bases).
Dwarf napiergrass was transplanted at three levels (1, 4 and 8 plants m
-2
) from cell-tray plants by Latin square
method in the University of Miyazaki (3183N, 13141E) on 2 July, 2010. Compound fertilizer containing 14%
of N, P
2
O
5
and K
2
O was applied monthly at 5 g each m
-2
time
-1
(annual total 20 g) and growth attributes of plant
height and tiller density were monitored monthly. Dry matter yield (DMY) of mother plants and efficiency of
nursery production using single-node stem cutting were determined per both land area and labor time on 8
December, 2010 and wintering ability was determined on 17 May, 2011 (Trial-1). Nursery plant was grown at
cell-tray bed in glasshouse during wintering from December to April and trimming effect on tillering ability of
nursery plants was checked on 13 April, 2011 (Trial-2). In Trial 1, plant height and tiller density increased with
increasing plant density and tiller density saturated earlier at 4 and 8 plants m
-2
than at 1 plant m
-2
. Although
DMY and number of nursery plants per mother plant was significantly higher (P < 0.05) at 1 plant m
-2
, those per
m
2
were significantly higher (P < 0.05) and labor time for nursery production per cutting, significantly lower (P <
0.05) at 4 and 8 plants m
-2
than at 1 plant m
-2
. Wintering ability was considerably high above 93% among 3
densities. In Trial-2, emerged percentage of nursery plants was consistent around 75% among 3 densities and
trimming increased tiller number to promote quicker establishment of nursery plants in the field. Thus, 4 and 8
plants m
-2
were concluded to be optimal for nursery production in the established year.

Keywords: dwarf napiergrass, nursery production, plant density, trimming, wintering ability.

Introduction

Napiergrass (Pennisetum purpureum Schumach) is a tropical C
4
grasses and its dry matter
yield was higher than other crops. Napiergrass can be used for multi-purpose uses such as feeding
to herbivores (Fukagawa et al., 2010; Utamy et al., 2011), rotational grazing use of dwarf variety
(Ishii et al., 2009), feedstock for bioethanol production (Khairani et al., 2010) and phytoremediation
activity (Hamano et al., 2011) in Kyushu, Japan. Napiergrass needs to be propagated vegetatively,
while efficient nursery production is not so established that the extension of this grass species is
hardly progressed. Therefore, in the present study, we examined the effect of mother plant density
on the efficiency of nursery production per both land area and labor time bases (Trial-1). In Trial-2,
we examined the effect of trimming on growth attributes of nursery plants, to obtain faster
establishment of this grass species.

th

Dwarf variety of late-heading type (DL) napiergrass, which was overwintered on a cell-tray
bed in a glasshouse from December 2009 to April 2010, was transplanted into the field at three
densities (1, 4 and 8 plants m
-2
) by Latin square method in University of Miyazaki (3183N,
13141E) on 2 July, 2010. Compound fertilizer containing 14% of N, P
2
O
5
and K
2
O was applied
monthly at 5 g each m
-2
time
-1
(annual total 20 g) and growth attributes of plant height and tiller
density were monitored monthly. Dry matter yield (DMY) of mother plants and efficiency of nursery
production using single-node stem cutting were determined per both land area and labor time on 8
December, 2010. Wintering ability, such as percentage of overwintered plants (POP) and regrown
tiller number (RTN), was determined on 17 May, 2011 (Trial-1). Nursery plant was grown at cell-tray
bed in a glasshouse during wintering from December to April and the effect of trimming at 5 cm
above the ground on tillering ability of nursery plants was checked to determine plant height, tiller
number and dry matter weight on 13 April, 2011. Additional fertilizer was supplied at 9.8 g N m
-2
on
16 April, 2010 (Trial-2).


Effect of mother plant density on growth rates of several plant attributes, dry matter
production and nursery plant production
With the increase in mother plant density, the growth rate of plant height and especially
number of tillers used for nursery production tended to increase and reached the stage of maximum
tiller density earlier in early August than at the lowest density of 1 plant m
-2
(Figure 1). Thereafter, it
occurred self-thinning to diminish less vigorous tillers and to decrease the tiller density at 4 and 8
plants m
-2
.
(A)
ns
0
20
40
60
80
100
120
140
160
180
1-Jul 1-Aug 1-Sep 1-Oct 1-Nov 1-Dec
P
l
a
n
t

h
e
i
g
h
t

(
c
m
1 plant m-2 4 plants m-2 8 plants m-2

(B)
ns
0
20
40
60
80
100
120
140
1-Jul 1-Aug 1-Sep 1-Oct 1-Nov
T
i
l
l
e
r

d
e
n
s
i
t
y

(
N
o

m
-
2
1 plant m-2 4 plants m-2 8 plants m-2

Figure 1. Changes in plant height (A) and tiller density (B) among three densities of mother plants.

Dry matter weight per plant was the highest at 1 plant m
-2
, followed by 4 and 8 plants m
-2
,
while dry matter yield per unit land area (m
2
) increased with the increase in mother plant density to
reach the highest yield (P < 0.05) at 8 plants m
-2
(Figure 2).
While number of nursery plants per mother plant was significantly higher (P < 0.05) at 1
plant m
-2
, those per m
2
were significantly higher (P < 0.05) and labor time for nursery production per
cutting, significantly lower (P < 0.05) at 4 and 8 plants m
-2
than at 1 plant m
-2
(Figure 3). Even
though plant leaf area was not determined in the present study, it is estimated that optimum leaf
area index (LAI) was attained at earlier stage to enhance dry matter yield in early December with
the increase in plant density. It is suggested that the period to make internode and node with tiller
buds matured would be proportional to periods from tiller emergence as the basis for matured tiller
buds suitable for nursery production. It is suggested that even delayed tillers emerged in early
September could be used for nursery production at 1 plant m-
2
, which did not have enough time for
tiller buds to matured (Figure 1 (B)).
th
These tiller productions also need more tillers to produce nursery plants, resulted in
extending time for nursery production and increasing cost of labor power at lower densities.

a
b
b
b
b
a
0
500
1000
1500
2000
2500
3000
plant Unit
area
plant Unit
area
plant Unit
area
1 4 8
D
M
W
(
g
)
Plant density (plants m
-2
) and per basis
D
ST
LB

a
b
b
b
b
a
0
500
1000
1500
2000
2500
3000
plant Unit
area
plant Unit
area
plant Unit
area
1 4 8
D
M
W
(
g
)
-2
) and per basis
D
ST
LB

Figure 2. Dry matter weight (DMW) of plant organs per both plant and unit area bases among three densities of
mother plants on 8 December 2010.
a
b
b
b
a
a
a
b b
0
100
200
300
400
500
600
700
0.0
0.1
0.2
0.3
0.4
0.5
1 4 8
N
o
.

o
f

n
u
r
s
e
r
y

p
l
a
n
t
s
L
a
b
o
r

t
i
m
e
m
a
n
m
i
n
u
t
e

n
u
r
s
e
r
y

p
l
a
n
t
-
1
)
-2
)
Nursery plant-1 Nursery m-2 Time

Figure 3. Nursery plant number and labor time for production per mother plant and per unit area.

Relationship between plant density of mother plants and sustainability of plants
In the present study, POP was hardly affected by plant density of mother plants and POP
overpassed 93% in all densities to show sustainability of this grass species. However, RTN per unit
land area (m
2
) tended to decrease consistently with the increase in mother plant density (Figure 4).
Since this phenomenon would affect negatively on maintaining tiller number for vegetative nursery
production and sustainability of mother plants, it is essential to continue examining the potential of
nursery production by these mother plants.
ns
50
60
70
80
90
100
0
5
10
15
20
25
30
1 4 8
P
O
P
T
i
l
l
e
r

d
e
n
s
i
t
y
N
o
.

m
-
2

-2
)
TN POP

Figure 4. Percentage of overwintered plants (POP, ) and regrown tiller density () on 17 May.

th
Effect of trimming on nursery plants
In Trial-2, emerged percentage of nursery plants was consistently 75% among 3 densities
at 2 months after planting (Figure 5). Trimming on nursery plants affected to increase tiller number
so as to promote quicker establishment of nursery plants in the field, even though plant height and
dry matter weight of nursery plants decreased by the trimming practice (data not shown).

Figure 5. Changes in emerged percentage of nursery plants among three densities of mother plants during
wintering period from early December 2010 to mid-May 2011.

In conclusion, 4 and 8 plants m
-2
were suggested to be optimal for nursery production in
the established year of DL napiergrass in southern Kyushu, Japan.

References

Fukagawa S, J Hirokawa, M Ookushi and Y Ishii. 2010. Fermentative quality and feed characteristics of dwarf
napiergrass (Pennisetum purpureum Schumach) silage. Japan. J. Grassl. Sci. 56: 26-33.
Hamano K, Y Ishii, A Yamano, K Mori, S Idota, DJ Kang, K Nakano, A Taniguchi and A Nishiwaki. 2011.
Development of low-cost phytoremediation techniques on heavy metal polluted soils by napiergrass
cultivation. Abstract for the 57th Meeting by the Association of the Kyushu Agricultural Research
Institute. Pp. 23. (In Japanese.)
Ishii Y, K Fukuyama, T Iwakiri, A Wadi and S Idota. 2009. Establishment of rotational grazing system on dwarf
napiergrass pasture oversown with Italian ryegrass by smallholder farmers of Japanese-Black breeding
beef cows in southern Kyushu, Japan. Proceedings of the 3rd Korea-China-Japan Joint Symposium on
Grassland Agriculture and Livestock Development. Pp. 218-219.
Khairani L, Y Ishii, S Idota, RF Utamy, A Yamano and A Nishiwaki. 2010. Nursery production and dry matter
productivity in six genotypes of napiergrass as biomass production in Southern Kyushu, Japan. Japan. J.
Grassl. Sci. 56 (Ext.) 14.
Utamy RF, Y Ishii, S Idota, N Harada and K Fukuyama. 2011. Adaptability of dwarf napiergrass under cut and
carry and grazing systems for smallholder beef farmers in southern Kyushu, Japan. J. Warm Region.
Soc. Anim. Sci., Japan. 54: 87-98.

th
Analysis of the Major Seed Storage Protein, 13S Globulin, in Common
Buckwheat (Fagopyrum esculentum Moench)

Tomoyuki Katsube-Tanaka
a,
*, Nadar Khan
a
, Yusuke Takahashi
a
,
Mariko Nakagawa
a

a
Graduate School of Agriculture, Kyoto University, Kitashirakawa, Kyoto 606-8502, Japan
* Corresponding author: Graduate School of Agriculture, Kyoto University, Kitashirakawa,
Kyoto 606-8502, Japan.
Tel.: +81-75-7536043; fax: +81-75-7536065.
[email protected]

Abstract

Common buckwheat seed proteins are valuable proteins with high nutritional and biological values. The proteins
are also health-promoting proteins with many physiological functions, such as the ability to lower blood
cholesterol and to prevent accumulation of fat, constipation, mammary carcinogenesis and colon
carcinogenesis. However, the proteins are allergenic to human beings. The elimination or mitigation of the
allergenic proteins is highly desired for the enhancement and potential utilization of buckwheat as a food crop.
The prevalent allergen of common buckwheat, Fag e 1, is polypeptide of the most abundant storage protein,
13S globulin. Because the 13S globulin is composed of multiple diversified subunits, polypeptide, the
counterpart of polypeptide in 13S globulin subunits, was characterized in depth in this study to better
understand this allergenic protein. The 13S globulin polypeptides were categorized into three types and were
further grouped into methionine-poor and methionine-rich subunits as major and minor types, respectively.
Besides the three known methionine-poor subunits, four new methionine-poor subunits with 0, 2, 4, and 6
tandem repeat inserts were identified. Highly polymorphic band pattern and its correlation between SDS-PAGE
and PCR analyses at a single seed level suggested that the large variation among the polypeptides was
explained by the different lengths of tandem repeat inserts. In agreement with the fact that the tandem repeat
region is hydrophilic with many arginine residues, digestibility against trypsin, that is one of critical characteristics
for food allergen, was different between the subunits with and without tandem repeat inserts.

Keywords: 13S globulin, seed storage protein, common buckwheat (Fagopyrum esculentum Moench)

Introduction

The allergens of buckwheat seeds have been identified and characterized by several
research groups. Even though the allergens varied among patient sera. Park et al. (2000) revealed
that the 9-, 16-, 19-, and 24-kDa proteins were the most prevalent allergens and that the 30-, 43-,
and 67-kDa proteins were the least prevalent allergens. The 24-kDa protein (named Fag e 1), which
is recognized as one of the most significant allergens by researchers, is the polypeptide of the
13S globulin. The Fag e 1-null mutant has been sought, but it has not been discovered. However,
the content of a Fag e 1 has been demonstrated to change among cultivars (Maruyama-Funatsuki
et al., 2004).
Buckwheat seeds contain 8.5% to 18.9% protein. The most abundant protein is the 13S
globulin, which is salt-soluble and accounts for approximately 43% of the total seed protein. The
13S globulin is a storage protein and resembles the legumin-like seed storage protein of other
species, such as rice glutelin and soybean glycinin. It is considered a member of the 11S globulin
family based on its sedimentation constant, amino acid homology and similarities in biosynthetic
and accumulation processes. Like other legumin-like, seed storage proteins (i.e., rice glutelin and
soybean glycinin), the buckwheat 13S globulin is composed of multiple subunits, each of which
contains acidic () and basic () polypeptides covalently linked by a disulfide bond.
th
The subunits of seed storage proteins show different characteristics from each other.
However, the subunit composition of buckwheat has seldom been of concern, except in some
studies by Cepkova & Dvoracek (2006), Rogl & Javornik (1996), and Bonafaccia et al. (1994). In
fact, even the differences in the subunit structures and the maximum number of subunit types are
not well known. To date, only four types of 13S globulin subunits have been identified.
In our current paper, we identified and characterized the polypeptides of the buckwheat
13S globulin by SDS-PAGE and 2D-PAGE, coupled with immunodetection using two unique
antibodies against the 13S globulin-related rice glutelin and soybean glycinin. Four new subunits
with various lengths of tandem repeats were confirmed by PCR analysis at a highly polymorphic
single seed level. By showing different digestibilities among the subunits, we proposed the
possibility to develop novel buckwheat plants with lowered allergenicity.


Plant materials and preparation of the 13S globulin
Flour and seeds of common buckwheat cultivar Shinano-ichigo were obtained from a
local milling company in the Nagano prefecture, Japan and a local nursery company in the Shiga
prefecture, Japan, respectively. Note that the commercial flour was made of uncounted number of
ground seeds and was expected to show averaged and practical characteristics in terms of protein
composition. Tartary buckwheat seeds of cultivar FT Rotundatiem were a gift from the National
Agricultural Research Center for Kyushu Okinawa Region. The protein fraction of the 13S globulin
was extracted from either a single seed flour or commercial flour with the extraction buffer (0.035 M
potassium phosphate, pH 7.6, and 0.4 M sodium chloride). The 13S globulin was either dissolved in
the sample buffer containing 50 mM Tris, pH 6.8, 2% (w/v) SDS, 0.1% (w/v) bromophenol blue,
10% (w/v) glycerol, and 5% (v/v) 2-mercaptoethanol for SDS-PAGE analysis or dissolved in the
lysis buffer containing 9.5 M urea, 2% Triton X-100, 5% 2-mercaptoethanol, and 5% Bio-Lyte 3-10
(Bio-Rad) for 2D-PAGE analysis.

SDS-PAGE, 2D-PAGE, and Western blot Analyses
SDS-PAGE was performed using 14%T acrylamide gel at a constant voltage of 200 V.
Isoelectric Focusing (IEF) was performed with IPG strips pH range 4-7 (BioRad) with a 7.5-cm
length according to the manufacturers instruction. Electrophoresis in the first dimension (IEF) was
performed at 200 V for 10 min, 400 V for 10 min, 1000 V for 10 min, and 1500 V for 12 hrs. The
immunoblotting was performed according to the method mentioned in our previous report (Khan et
al., 2008). Anti-rice glutelin and anti-soybean glycinin antibodies (Katsube-Tanaka et al., 2004;
Katsube et al., 1999) were used to detect the 13S globulin polypeptides of common buckwheat.

Genomic DNA extraction and PCR Analysis
Genomic DNA extraction from the Shinano-ichigo single seeds and PCR analysis were
performed according to a kit (Ampdirect plus, Shimadzu, Japan). The primers used over the tandem
repeat region around 433-663 bp from the 5-end of the GenBank accession gene D87980 were as
follows: forward (left1), AGGATG(C/T)CCGGAGAC(A/G)T(A/T)CCA and reverse (right1),
CTAACGTTC(C/T)CATCGAGCTG for the Met-poor subunits.

Trypsin digestion
Globulin fractions extracted from the Shinano-ichigo buckwheat flour were incubated with
1/100 (w/w) trypsin (Promega, sequence grade) for two hours at 37C according to the
manufacturers instruction. Aliquots taken at a given times were electrophoresed and compared by
CBB staining and western blotting with the anti-glutelin antibody.

th

The 13S globulin fractions from commercial flour of common buckwheat and tartary
buckwheat seeds were resolved by SDS-PAGE, and detected by immunodetection using anti-
glycinin and anti-glutelin antibodies. The polypeptides of common buckwheat cv. Shinano-ichigo
were separated into at least 9 major bands (a2-a10) and those of tartary buckwheat were into 7
major bands (ax, a1, a6-a10) (data not shown). The polypeptides of common buckwheat were
ranged from 30 to 47 kDa according to the mobility in SDS-PAGE.
For a detailed understanding in the variations of the 13S globulin polypeptides, 13S
globulin polypeptides from Shinano-ichigo commercial flour were analyzed by 2D-PAGE using
anti-glycinin and anti-glutelin antibodies. The major 8 bands recorded on SDS-PAGE gels were
resolved into several distinct spots with different pI values and with slightly different molecular
weights on 2D-PAGE gels, forming a horizontal streak (data not shown). Each horizontal streak of
spots was collectively named, instead of naming each spot individually in this study. When the spots
were examined with the anti-glycinin and anti-glutelin antibodies, most spots reacted against either
of two antibodies with different degrees except the spot a9.
D87980
AF152003
D87982
AY256960
Met-poor subunit
o SP |
tandem repeats (5)
Met-rich subunit
tandem repeats (3)
tandem repeat (1)
o SP |
0.35 1.06
0.37 1.12
0.40 1.19
3.53 1.55
Mol%
41.3 21.1
37.5 21.5
33.5 21.4
28.5 20.2
Met Cys
kDa

5.2 9.1
5.4 9.2
5.2 9.7
5.0 6.7
pI

Figure 1. Schematic representation of the 13S globulin subunits.

Primary structures of the known 13S globulin subunits (pro-form, and polypeptide with
signal peptide) of common buckwheat were compared (GenBank accession No. D87980,
AF152003, D87982, AY256960). The subunits are classified as Met-poor and Met-rich according to
the methionine content of each subunit. The Met-poor subunits have tandem repeats with different
lengths (shown as a number in brackets with the polypeptide). Horizontal arrows denote the
position for PCR primers.
A database search and the organization of all retrieved data showed the existence of three
types of methionine scarce subunits (Met-poor subunits) and one methionine abounding subunit
(Met-rich subunit) (Fig. 1). The three Met-poor subunits contain variable tandem repeat sequences.
For example, GenBank accessions D87982, AF152003, and D87980 have one, three, and five
tandem repeats respectively, whereas the Met-rich subunit of GenBank accession AY256960 has
no tandem repeat sequence. Because the number of types observed in the SDS-PAGE of the
polypeptides were greater than the number of known subunits, PCR primers were designed at
conserved positions (horizontal arrows, Fig. 1) over the region containing the tandem repeats of the
Met-poor subunit to explore novel genes. The PCR amplification with the crude genomic DNA
produced seven types of bands, which were named mp2-mp8 (data not shown). The DNA
th
sequences of the representative amplified bands (mp2-mp8) were determined and aligned with the
Met-poor subunits of the GenBank accessions: D87980, AF152003, and D87982. The sequence
analysis revealed that the clones for bands mp3, mp5, and mp7 correspond to D87980, AF152003,
and D87982, respectively. Additionally, the clones for bands mp2, mp4, mp6, and mp8 were from
novel genes with 6, 4, 2, and 0 tandem repeats, respectively.
When the PCR band patterns were compared with SDS-PAGE patterns examined using
the same seeds with those for PCR analysis, the occurrence pattern of the band mp3 showed good
correlation with that of the SDS-PAGE band a3 (data not shown). In addition, the mp2-mp8 bands
and a2-a8 bands were observed at equally spaced intervals (data not shown). The above results
led us to hypothesize that the a2-a8 bands are correlated with mp2-mp8, respectively. In other
words, the bands a2, a3, a4, a5, a6, a7, and a8 have 6, 5, 4, 3, 2, 1, and no tandem repeats,
respectively.
The amino acid sequences deduced from PCR amplified bands mp2-mp8 were compared
with those of D87980, AF152003, and D87982 (Fig. 2). The alignment clearly showed the tandem
repeat regions had less diversity, except the lengths of the bands. However, it is notable that the
tandem repeat regions and their vicinities had many arginine residues, and the regions were
hydrophilic according to a method used by Kyte & Doolittle (1982), indicating the regions are likely
to be exposed at the molecular surface. This feature of the tandem repeat regions strongly suggests
the regions are susceptible to trypsin.
10 20 30 40 50 60
. . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . |
mp2 S ES E YP QS QRDQRS RQS ES E ES S RGDQR T RQS ES E E F S RGDQR T RQS ES E E F S RGDQR T R
D87980 S E F E YP QS QRDQRS RQS ES E ES S RGDQR T RQS ES E E F S RGDQR T RQS ES E E F S RGDQR T R
mp3 S ES E YP QS QRDQP S RQS ES E E F S RGDQR T RQS ES EGF S RGDQR T RQS ES E E F S RGDQR T R
mp4 S E F E YP R F QRDQRS RQS ES E ES S RRDQRS RQS ES E ES S RGDQRS RQS ES V ES S RGDQRS R
AF152003 S E F E YP RS QRDQRS RQS ES GES S RGDQRS RQS ES E ES S RGDQRS RQS ES E E F S RG~ ~ ~ ~ ~
mp5 S E F E YP QS QRDQRS RQS ES E ES S RGDQR T RQS ES E E F S RGDQR T RQS ES E E F S RG~ ~ ~ ~ ~
mp6 S E F E YP RS ERGRHS RQS ES E ES S RGDQS S RQS ES E ES S RG~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~
D87982 S E F E YP QS QRGRHS RQS ES E E ES S RG~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~
mp7 S E F E YP QS QRGRHS RQS K T E E ES S RG~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~
mp8 S E F QS ES ES S RS I S ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~
70 80 90 100 110 120
. . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . | . . . . |
mp2 QS ES E E F S RGDQR T RQS ES E E F S RGDQR T RQS EGE E F S RGDQHQK I F R I RDGDV I P S P AG
D87980 QS ES E E F S RGDQR T RQS ES E E F S RG~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ DQHQK I F R I RDGDV I P S P AG
mp3 QS ES E E F S RGDQR T RQS ES E E F S RG~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ DQHQK I F G I RDGDV I P S P AG
mp4 QS ES E ES CQG~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ DQHQK I F R I RDGDV I P S P AG
AF152003 ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ DQHQK I F R I RDGDV I P S P AG
mp5 ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ DQHQK I F R I R EGDV I P S P AG
mp6 ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ DQHQK I F R I R EGDV I P S P AG
D87982 ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ DQHQK I F R I R EGDV I P S P AG
mp7 ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ DQHQK I F R I RDGDV I P S P AG
mp8 ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ ~ D EHQKV F R I R EGDV I P S P AG
mp2
D87980
mp3
mp4
AF152003
mp5
mp6
D87982
mp7
mp8
Tandem repeat 1 Tandem repeat 2 Tandem repeat 3
Tandem repeat 4 Tandem repeat 5 Tandem repeat 6
Hydrophilic

Figure 2. Deduced amino acid sequences and hydrophobicities over the tandem repeat inserts of the Met-poor
subunits.

The amino acid sequences deduced from the PCR bands amplified for the Met-poor
subunits (mp2-mp8) were compared with that of D87980, AF152003, and D87982. The amino acids
spanning 108-212 residues from the N-terminus of the mature polypeptides (D87980) were
aligned. The position of tandem repeats 1-6 and approximate hydrophilic area were shown by
double-headed arrows and gray color shades, respectively.
Trypsin digestions demonstrated that most of the 13S globulin polypeptides degraded
within two hours except for the a8 band, which is likely to have no tandem repeat (data not shown).
The intensity of the a8 band detected by anti-glutelin stayed nearly constant during the reaction,
and no new, polypeptides were detected, suggesting the degradation occurred not only at a
tandem repeat region but also with the entire polypeptide sequence. Notably, the a9 band, which
th
seems to be derived from a Met-rich subunit having relatively higher cysteine contents, was rather
resistant to digestion according to the CBB staining (data not shown).
It has been described that resistance to digestion and processing is one of the more
important characteristics for food allergenic proteins (Bannon, 2004). Sen et al. (2002) showed
peanut allergenic protein stability upon proteinase digestion affected IgE-binding epitopes
intactness. Even though the difference in the digestibility of the polypeptides was empirically not
revealed in this study, the tandem repeat insertion into the polypeptides might have influenced the
polypeptide conformation as well by a conserved inter-polypeptide disulfide bond with one of the
involved Cys residues located 18-residues upstream from the tandem repeats. If the hypothesis is
correct, the Met-poor subunits of the 13S globulin may have different digestibilities and distinct
potential allergenicities. Although our preliminary analysis on pepsin digestibility demonstrated little
difference among the subunits (data not shown), reducing the content of the trypsin-resistant
subunit, the a8 polypeptide with no tandem repeats, might be useful for the development of novel
buckwheat with lowered allergenicity. Further investigation on IgE binding of buckwheat
hypersensitive patients sera should be required.

Acknowledgements

The authors thank Mr. Satoru Yamaguchi for his technical assistance. Germplasms of tartary
buckwheat seeds were kindly provided by the National Agricultural Research Center for Kyushu Okinawa
Region. This work was supported in part by grants to T.K.-T. from the Ministry of Education, Culture, Sports,
Science, and Technology, Japan for Scientific Research (C) (20580013, 2008-2010; 23580020, 2011-2013) and
by a fellowship to N. K. from the Japan Society for the Promotion of Science.

References

Bannon GA. 2004. What Makes a Food Protein an Allergen? Current Allergy and Asthma Reports 4: 4346.
Bonafaccia G, R Acquistucci and Z Luthar. 1994. Proximate chemical composition and protein characterization
of the buckwheat cultivated in Italy. Fagopyrum 14: 4348.
Cepkova P and V Dvoracek. 2006. Seed protein polymorphism of four common buckwheat varieties registered
in the Czech Republic. Fagopyrum 23: 1722.
Katsube T, N Kurisaka, M Ogawa, N Maruyama, R Ohtsuka, S Utsumi and F Takaiwa. 1999. Accumulation of
soybean glycinin and its assembly with the glutelins in rice. Plant Physiology 120: 10631074.
Katsube-Tanaka T, JB Duldulao, Y Kimura, S Iida, T Yamaguchi, J Nakano and S Utsumi. 2004. The two
subfamilies of rice glutelin differ in both primary and higher-order structures. Biochimica et Biophysica
Acta (BBA) - Proteins & Proteomics 1699: 95102.
Khan N, T Katsube-Tanaka, S Iida, T Yamaguchi, J Nakano and H Tsujimoto. 2008. Identification and variation
of glutelin polypeptides in the genus Oryza assessed by two dimensional electrophoresis and step-by-
step immuno detection. Journal of Agricultural and Food Chemistry 56: 49554961.
Kyte J and RF Doolittle. 1982. A Simple Method for Displaying the Hydrophobic Character of a Protein. Journal
of Molecular Biology 157: 105132.
Maruyama-Funatsuki W, K Fujino, T Suzuki and H Funatsuki. 2004. Quantification of a major allergenic protein
in common buckwheat cultivars by an enzyme-linked immunosorbent assay (ELISA). Fagopyrum 21:
3944.
Park JW, DB Kang, CW Kim, SH Ko, HY Yum, KE Kim, CS Hong and KY Lee. 2000. Identification and
characterization of the major allergens of buckwheat. Allergy 55: 10351041.
Rogl S and B Javornik. 1996. Seed protein variation for identification of common buckwheat (Fagopyrum
esculentum Moench) cultivars. Euphytica 87: 111117.
Sen M, R Kopper, L Pons, EC Abraham, AW Burks and GA Bannon. 2002. Protein structure plays a critical role
in peanut allergen stability and may determine immunodominant IgE-binding epitopes. The Journal of
Immunology 169: 882-887.
-- back to Table of Content
th
th
Isolation of soc-tuf Gene Encoding Chloroplast Elongation Factor
Tu (EF - Tu) Protein from Sugarcane (Saccharum officinarum)

Dhika Amanda
a
, Sony Suhandono
b

*

School of Science and Technology, Institut Teknologi Bandung,
LABTEK XI-Genetic Laboratory, Ganeca 10, Bandung 40132, Indonesia.
Tel.: +62 22 251-1575; +62 22 250-0258; fax: +62 22 253-4107. [email protected] ;

Abstract

Molecular chaperone is a molecule preventing the aggregation, denaturation, and inactivation of various proteins
when the cells were exposed to extreme environmental conditions, such as high temperature or drought. One of
such proteins is an Elongation factor Tu (EF - Tu). We have isolated an elongation factor Tu gene from
sugarcane from cDNA which was heat-treated at 45C for 16 h using reverse transcriptase PCR. The isolation
was made in two steps. The first steps using internal primer developed using tuf gene sequence from maize
available in the GenBank. Since partial cDNA sequence needs to be filled in, the sequence from sugarcane
which is available in KEGG genome was added into a new primer designed to make overlapped PCR. This
technique was used to clone the gene into bacterial expression vector pET-32b in order to test the soc-tuf gene
function as molecular chaperone in bacterial system. The results showed that the gene had homology of 94%
with maize tuf gene and 97% with sorghum amino acid sequence. The deduced amino acid sequence had
homology of 92% with maize and 95% with sorghum, respectively. Gene analysis was conducted by generate
phylogenetic molecular tree. Based on the tree, Sugarcane tuf sequence was actually clustered with Sorghum
bicolor and Zea mays sequence. Thus, it had high possibility that soc-tuf gene from sugarcane having similar
motif, protein structure, and can function as molecular chaperone as tuf gene from maize.

Keywords: chloroplast protein elongation, environmental stress, heat tolerance, sugarcane (Saccharum
officinarum)

Introduction

Elongation factor Tu (EF - Tu) is a protein that involved in translational process. By binding
to GTP and aminoacyl tRNA, EF - Tu also translocate them into ribosome A-site (Brot, 1977; Riis,
et al., 1990). EF - Tu has three domains GTP-binding protein which also has similar characteristic
with Ras proteins superfamily (Warren, et al., 2001) belongs to the family of G proteins and is highly
conserved in all organisms (Bhadula et al., 2001).
EF Tu in organelles (chloroplast and mitochondria) has the same function as EF - 1 in
eukaryotic cytosol (Miller & Wissbach, 1977). Interestingly, the organellar EF Tu shows more
similarities to prokaryotic EF Tu than to eukaryotic EF - 1 (Lee, et al., 1999). Previous studies
show that chloroplast EF Tu has 80% similarity to prokaryotic EF - Tu and has 80 90% similarity
to other EF Tu from higher plants (Bhadula et al., 2001; Riis, et al., 1990). This is reflects their
origin via ancient endosymbiosis (Gray, 1992). In most of lower photosynthetic eukaryotes,
chloroplast elongation factor Tu (EF - Tu) is encoded by tuf gene in chloroplast genome (Baldauf &
Palmer, 1990). While in higher plants, the genes encoding EF Tu are located in the nucleus
(Moriarty, et al., 2002; Baldauf & Palmer, 1990) and after translation, the protein is transported into
chloroplast.
In prokaryotes, EF - Tu is also involved in heat tolerance mechanism as molecular
chaperones, that prevent the degradation of cellular proteins during heat stress, increase the
refolding of unfolded proteins, and increase the stability of protein (Moriarty, et al., 2002; Momcilovic
& Ristic, 2004; Rao, et al., 2004 Ristic, et al., 2008). During heat shock treatments, EFTu
th
molecules are accumulated in cytoplasm and near cytoplasmic membrane of E. coli (Caldas, et al.,
1998). Moreover, E. coli EFTu protein has ability to remain soluble and maintain its activity to 45C
(Caldas, et al., 1998). It also binds other proteins and extends their stability up to 50C (Caldas, et
al., 1998). Previous studies showed that plants also expressed chloroplast EFTu protein when it
was exposed to high temperatures (Momcilovic & Ristic, 2004; 2007; Rao, et al., 2004; Ristic, et al.,
2004; 2008). Exposure to a long term heat stress increased the level of chloroplast EFTu protein in
mature wheat plants (Ristic et al., 2008). The level of heat-induced EFTu protein in heat-tolerance
wheat cultivars is greater than EFTu level in heat-sensitive cultivars (Ristic et al., 2008). The same
pattern was also observed in maize that heat sensitive maize line ZPL 389 did not accumulate EF-
Tu under heat stress, while heat tolerant line ZPBL 1304 accumulate EFTu (Momcilovic & Ristic,
2004; 2007). Therefore, only plants, which show better tolerance to heat stress, express high
amount of heat-induced EFTu protein. However, the evidence that chloroplast EF-Tu protein
involved in heat tolerance, so far, reported only in maize (Bhadula et al., 2001; Momcilovic & Ristic,
2004; Rao et al., 2004; Ristic et al., 2004).
In this study, EF-Tu from sugarcane (Saccharum officinarum) was used. Sugarcane is C4
plant commonly found in Southeast Asia region. Sugarcane has 3-4 times longer harvesting period
than maize. It is assumed that sugarcane has been exposed to heat stress longer than maize and
have higher temperature tolerance. The purposes of this research were to isolate soc-tuf gene
encoding chloroplast elongation factor Tu (EF-Tu) from sugarcane and to investigate the gene
similarities using phylogenetic tree. Therefore, this study was conducted based on the hypotheses,
if soc-tuf gene is significantly homologous with tuf from maize or highly conserved, thus there is
possibility that the protein may function to increase heat tolerance.


Samples preparation and treatment with high temperature
In this study, sugarcane plantlets with approximately of 4-6 cm of length were used. Before
isolation, the plantlets were treated with different duration of incubation. Sugarcane plantlets were
incubated at 45C (Ristic, et al., 2002) in incubator for 2, 4, 6, 14, and 16 h. The same treatment
was also made to control plantlets exposed at 37C. Sugarcane from each treatment was taken and
cleaned from the attached medium. Then, 600 mg of samples were used for RNA isolation total
RNA from sugarcane was isolated by using Trizol
Solution Kit (Sigma, USA), followed by cDNA

synthesis.

Primer design and tuf gene isolation from cDNA samples
There was no publication on sugarcane tuf gene so far, thus forward primer EF-TU-S for
tuf gene amplification was designed by using maize tuf sequence. Meanwhile, maize reverse primer
DO35690 (5-TTACCACCCTCACGGATAGCAAACCTC-3) (Ristic, et al., 2004) was used to amplify
sugarcane tuf gene. It was assumed that these primers will amplify about 1370 bp of sugarcane tuf
gene. Amplification was generated using KAPA 2G
TM
Robust HotStart PCR system (KAPA
Biosystems, USA) and sugarcane cDNA was used as a template.

Construction of full length tuf gene using overlap-extension PCR
Based on multiple sequence alignment, the amplified sugarcane tuf gene was not
completed. To obtain full length sequence, sugarcane sequence was aligned with sugarcane EST
from KEGG genome (http://www.genome.jp/kegg). Reverse primer was designed containing both
sugarcane consensus sequence and expression vector sequence. While forward primer was
designed containing both of soc-tuf partial sequence and expression vector sequence. Primers
used to generate overlap-extension PCR were, forward primer EFTU-DA.F1 and reverse primer
EFTU-DA.R1, respectively. Amplification was generated by using Phusion
Polymerase PCR
th
system (Finnzymes, USA) with touchdown PCR. Samples were visualized using DNA
electrophoresis. Relevant DNA fragment was extracted from agarose gel and purified for further
study.

Construction of tuf gene into expression vector pET-32b using PCR-cloning
In order to investigate the ability of sugarcane tuf gene, the gene was inserted into an
expression vector pET-32b using PCR cloning (Bryksin & Matsumura, 2010). Instead of using two
type of primer (forward and reverse primer), PCR cloning only used one DNA fragment derived from
overlapextension PCR product containing the gene of interest and two vector-homologous
sequence at 3 and 5- end of the sequence. This vector-homologous sequence acts as a primer
and anneals to the plasmid vector to initiate the amplification.

Sequence analysis and construction of phylogenetic tree
Multiple sequence alignment was generated using CLUSTAL W in Bioedit and Geneious
alignment in Geneious 4.8.5. Nucleotide and amino acid homology were analyzed using BLASTn
and BLASTx from NCBI (http:// www.ncbi.nlm.nih.gov). Phylogenetic tree was constructed using
MEGA 5.0 software.


Nucleotide sequence homology and similarity analysis
Based on BLASTn result (Table 1), sugarcane tuf sequence had 97% homology to
Sorghum bicolor hypothetical protein sequence with 100% query coverage. Sorghum bicolor
hypothetical protein has not been annotated yet. However, this protein has similar characteristics
with EF-Tu proteins. In order to make the result more reliable, sugarcane tuf sequence was aligned
with maize sequence and the result showed that sugarcane sequence had 94% similarity with
maize tuf sequence encoding elongation factor Tu (EFTu) with 100% query coverage. E-value for
these alignments are 0, thus the result was reliable.

Table 1. BLASTn result from sugarcane EF - Tu sequence using eucaryotes database
Accession
Number
Species
Query
Coverage
E-value Homology
XM_002452345.1 Sorghum bicolor hypothetical protein, mRNA 100% 0 97%
NM_001156938.1
Zea mays elongation factor Tu
(LOC100284040), mRNA >gb|EU966875.1|
Zea mays clone 297889 elongation factor Tu
mRNA, complete cds
100% 0 94%

In order to predict whether the nucleotide differences within sugarcane sequence has
frame shift effect at amino acid sequence or not, sugarcane sequence must be analyzed by using
BLASTx. Based on BLASTn result, sugarcane tuf sequence had 97% homology to Sorghum bicolor
hypothetical protein sequence with 100% query coverage. The result (Table 2) showed that the
differences within sugarcane nucleotide residues do not change amino acid sequence significantly.
Sugarcane sequence still had 95% homology with Sorghum bicolor hypothetical protein and also
92% homology with Zea mays elongation factor Tu.
In order to investigate the homology between sugarcane and procaryotes tuf sequence,
another BLASTx and BLASTn were conducted using procaryotes protein database. Based on
BLASTn result, sugarcane tuf sequence had 67% homology to Escherichia coli (acc.
th
ZP_07125171.1) elongation factor Tu sequence with 90% query coverage. Moreover, The BLASTx
result (Table 3) showed that sugarcane sequence still had 70% homology with Thermus
scotoductus SA-01 and Thermus Aquaticus elongation factor Tu, also had 69% homology with
Thermus thermophilus HB27 elongation factor Tu.

Table 2. BLASTx result from sugarcane EF - Tu sequence using eucaryotes database

Accession
Number
Species
Query
Coverage
E-value Homology
XP_002452390.1
Sorghum bicolor hypothetical protein
SORBIDRAFT_04g024850 >gb|EES05366.1|
99% 0 95%
NP_001149568.1
Zea mays LOC100283194 >gb|ACG35888.1|
Zea mays elongation factor Tu
99% 0 92%

Table 3. BLASTx result from sugarcane EF - Tu sequence using procaryotes database

Accession
Number
Species
Query
Coverage
E-value Homology
YP_004201365.1 Elongation factor Tu [Thermus scotoductus SA-01] 90% 3e-149 70%
1EFT_A
The crystal structure of elongation factor EF-Tu from
Thermus Aquaticus
90% 3e-149 70%
YP_005299.1 Elongation factor Tu [Thermus thermophilus HB27] 90% 1e-148 69%

Based on BLAST results, it can be concluded that the sequence isolated from sugarcane
was the tuf gene coding sequence. Characterization of sugarcane tuf gene was conducted by using
various bioinformatics tools. FGENESH 2.6 from Softberry (www.softberry.com showed that soc-tuf
cDNA sequence consisted of 1404 nucleotide residue which encodes 466 amino acid.

Construction of phylogenetic tree
Phylogenetic tree (Figure 1) of tuf sequences constructed based on sample sequence
aligned with the various tuf sequences which were retrieved from GenBank and analyzed using
Neighbor-Joining method with Kimura 2 parameter. The phylogenetic tree will confirm the BLASTn
result. Tentative result of the BLASTn was used to collect other sequence related to the sample
sequence, and construct the tree.
Sugarcane sequence is clustered with Sorghum bicolor with value 0.021 and Zea mays
sequence with value 0.055 and also clustered at the same group as Oryza sativa with value 0.115
and Triticum aestivum with value 0.117 which belong to Poaceae family (the scale or branch length
refers to the evolutionary distances used to infer the phylogenetic tree).
Based on sequence homology, several groups were formed with Thermus thermophilus as
an outgroup. The homology of tuf sequence within plants (intra-clade) were higher than the inter-
clade homology of tuf sequence. Thus, plant species formed a single cluster. While, bacterial
species also formed a single cluster. Sugarcane sequence is actually clustered with Sorghum
bicolor and Zea mays sequence at almost no nucleotide difference. It is also clustered at the same
group as Oryza sativa and Triticum aestivum which are belong to Poaceae family. Due to soc-tuf
gene has significant homology with maize tuf, thus there is high possibility that it also has similar
motif, protein structure, and can function as molecular chaperone as tuf gene from maize in order to
improve heat tolerance abillity in organisms.

th
gi|24030502 Arabidopsis thaliana
gi|297791346 Arabidopsis lyrata
Brassicaceae
Solanaceae gi|459238 Nicotiana sylvestris
Euphorbiaceae 17519750/1-1281 Cassava
Geraniaceae gi|12830554 Pelargonium graveolens
Fabaceae gi|292774551 Lotus japonicus
Papilionaceae gi|18775 Glycine max
gi|241985081 Triticum aestivum
gi|6525064 Oryza sativa
gi|226508703 Zea mays
gi|242062201 Sorghum bicolor
Saccharum officinarum
Poaceae
Bacillaceae gi|255767013 Bacillus subtilis
Moraxellaceae gi|169794206 Acinetobacter baumannii
gi|207855516 Salmonella enterica
gb|AE014075.1 Escherichia coli
Enterobacteriaceae
Thermaceae gi|48287 Thermus thermophilus
100
64
100
99
100
54
100
99
100
76
95
55
88
0.00 0.05 0.10 0.15 0.20

Figure 1. Neighbor-joining tree of tuf gene sequence using Kimura 2 parameter model with Gamma distribution.

References

Baldauf, S.L., J.D. Palmer. 1990. Evolutionary transfer of the chloroplast tufA gene to the nucleus. Nature. 344:
262 - 265.
Bhadula, S.K., T.E. Elthon, J.E. Habben, T.G. Helentjaris, S. Jiao, Z. Ristic. 2001. Heat stress induced synthesis
of chloroplast protein synthesis elongation factor (EF-Tu) in a heat-tolerant maize line. Planta. 6:212-
359.
Brot, N. 1977. Molecular Mechanism of protein synthesis. (H. Weissbach, & S. Pestka, Eds.). Academic Press,
New York.
Bryksin, A.V., I. Matsumura. 2010. Overlap extension PCR cloning: a simple and reliable way to create
recombinant plasmids. BioTech. 48: 463 - 465.
Caldas, T., A. Yaagoubi, G. Richarme. 1998. Chaperone properties of bacterial elongation factor EF-Tu. Biol.
Chem. 273: 11478 - 11482.
Gray, M.W. 1992. The endosymbion hypothesis revisited. Int. Rev, Cytol. 141: 233 - 357.
Lee, J.H., J.W. Lee, Y-Y. Chung, K.H. Paek, J.S. Shin, C-H. Yun. 1999. Cloning and characterization of
chloroplast elongation factor EF-Tu cDNA of Oryza sativa L. Mol. Cells. 9 (5): 484 - 490.
Momcilovic, I., Z. Ristic. 2007. Expression of chloroplast protein synthesis elongation factor, EF-Tu, in two lines
of maize with contrasting tolerance to heat stress during early stages of plant develoment. Plant Physiol.
164: 90 - 99.
Momcilovic, I., Z. Ristic. 2004. Localization and abundance of chloroplast protein synthesis elongation factor
(EF-Tu) and heat stability of chloroplast stromal protein in maize. Plant Sci. 81 - 88.
Moriarty, T., R. West, G. Small, D. Rao, Z. Ristic. 2002. Heterologous expression of maize chloroplast protein
synthesis elongation factor (EF-Tu) enhances Escherichia coli viability under heat stress. Plant Sci. 163:
1075 1082.
Rao, D., I. Momcilovic, S. Kobayashi, E. Callegari, Z. Ristic. 2004. Chaperone activity of recombinant maize
chloroplast protein synthesis elongation factor, EF-Tu. Eur J. Biochem. 271: 3684 - 3692.
Riis, B., S.I. Rattan, B.F. Clarck, W.C. Merrick. 1990. Eukaryotic Protein Elongation Factors. Treds Biol. Sci. 15:
420 - 424.
Ristic, Z., U. Bukovnik, I. Momcilovic, J. Fu, P.V. Prasad. 2008. Heat-induced accumulation of chloroplast
protein synthesis elongation factor, EF-Tu, in winter wheat. Journal of plant physiology. Plant Physiol.
165: 192 202.
Ristic, Z., K. Wilson, C. Nelsen, I. Momcilovic, S. Kobayashi, R. Meeley. 2004. A maize mutant with decreased
capacity of accumulate chloroplast protein synthesis elongation factor (EF-Tu) displays reduced
tolerance to heat stress. Plant Sci. 167: 1367 1374.
Warren, C., I. Lathe, B. Peer. 2001. Evolution of tuf genes: ancient duplication, differential loss, and gene
conversion. FEBS Letters. 502: 113 - 116.
th
Endophyte Microbes from Oil Palm (Elaeis guineensis) Tissues and Its
Potential as a Biocontrol for Ganoderma boninense In Vitro

Wisnu Adi Wicaksono, Rika Fithri Buana, Elizabeth Caroline Situmorang

Plant Production and Biotechnology Division,PT SMART Tbk, Bogor, Indonesia
*
)
Corresponding author: Plant Production and Biotechnology Division, PT SMART Tbk
Jl. Raya Padjajaran No 78 FG, Bogor, Indonesia
Tel.: +6251 8310854; fax: + 6251 8310854
[email protected]

Abstract

Endophyte microbes are microbes that colonize internal plant tissues without causing visible damage to their
host plant and they can act as promising biological control agents in oil palm. The objective of this research is to
obtain endophyte microbes which produce high chitinase activity and can inhibit G. boninense growth.
Endophyte microbes are isolated from roots of oil palm planted in Padang Halaban estate, North Sumatera. Dual
culture are performed in PDA medium using G. boninense from field. Chitinase assay was measured by
spectrophotometry method. Potential isolates have been identified based on ITS rDNA using ITS1 and ITS4
primers for fungi and based on 16S rDNA using 9F and 1510R for bacteria. These endophyte fungi can inhibit G.
boninense growth with inhibition ratio < 64%. T1 isolate has the highest activity of chitinase with 2.07 U/mL.
There are four potential isolates of endophyte fungi: Aspergillus, Fusarium, Hypocrea, and Trichoderma. B2.1.2
isolate of bacteria has the highest inhibition ratio (67%) but B13.10.4 isolate has the highest chitinase activity
with 3.43 U/mL. This result can be assumed that inhibition activity do not have any corelation with chitinase
activity. The identification of potential isolates showed that they are Serratia, Burkholderia, Acinetobacter, and
Bacillus.

Keywords: root-endophytes microbe, Ganoderma boninense, Elaeis guineensis, chitinase activity, ITS rDNA,
16S rDNA

Introduction

Basal stem rot (BSR) disease caused by Ganoderma boninense is the most destructive
disease in oil palm industries (Flood et al. 2000). Mostly, visible disease symptoms of BSR would
appear at a late stage. Development of BSR infection could happen at 6 until 12 months (Darmono,
1996). The infected oil palm would decay at basal tissue with the result that infected plant would fall
down before the economical time. At the endemic location, plant could infected less than 2 years of
planting period. Many strategies have been conducted to control BSR included cultural, chemical
and clean clearing. Unfortunately, those strategies have not been successful, for example, the use
of chemical fungicide in the field has not been proven as an effective control method (Sapak et al.,
2008).
Biological control can be promising strategy to control BSR. One of microbes group which
could use for biocontrol agent is endophyte microbes. Endophyte microbes is microbes that
colonize internal plant tissues without causing visible damage to their host plant. Recent surveys of
various host plants have demonstrated that endophyte microbes are ubiquitous in plant species
(Shiomi et al., 2006). As internal colonisers, therefore they are more able to compete within the
vascular systems with capacity to prevent infection of G. boninense.
The objective of this study was to isolate the endophyte microbes for G. boninense
biocontrol based on antagonistic characteristic and chitinase activity and also to identify endophyte
microbes based on ribosomal DNA.

th

Root sampling and isolation of endophyte microbe
Oil palm roots were obtained from Padang Halaban Estate PT SMART, Tbk in North
Sumatera, Indonesia. The age of palm was 28 years with symptomless BSR (Basal Stem Rot) at
endemic areas. Random palms were sampled with the roots diameter 0.5 cm, taken about 1.0 m
away from their bases at 25 30 cm depth.
Root samples were surface sterilized by dipping in 5.25 % sodium hypochlorite, and
subsequently in 50, 70, and 90 % of ethanol then rinsed twice with sterilized water. Root section
was transferred to Nutrient Agar (NA) for bacteria culture and Potato Dextrose Agar (PDA) for fungi.
For bacteria were incubated at 37
o
C and for fungi at 28
o
C.

Microscopy observation of endophyte microbes
a. Bacteria Gram staining. One loop of bacteria was dropped onto a slide glass and air
dried. The slide was stained with crystal violet for 1 min and then washed with alcohol, iodine for 1
min, and distilled water respectively. After that, the slide was added with safranin for one min and
washed again with distilled water to remove any staining solution. The slide was examined under a
bright-field microscope (Model Nikon Eclipse-50i, Japan).
b. Morphological and histological identification of fungal endophytes. Morphological
identification of fungal isolates was according to colony or hyphal morphology of the fungal culture,
surface and reverse colony color, and colony texture. Histological identification of fungal
endophytes was carried out by observing the characteristics of the spores or conidia, and
reproductive structures (sexual and asexual) under a bright-field microscope (Model Nikon Eclipse-
50i, Japan).

In vitro screening of endophyte microbe against G.boninense
The endophytes microbe isolates were screened for characteristic to inhibit G. boninese in
vitro by dual culture test and chitinolytic activity assay.
Dual culture test (Jinantana & Syariah 1997). A 5 mm diameter agar disc was taken from a
week-old PDA culture of G. boninense. For bacteria, agar disc with G. boninense was placed in
central PDA and 6 cm diameter filter paper with 24 hours old of endophyte bacteria was placed
around of G. boninense isolate. For fungi, agar disc with G. boninense was placed 6 cm away from
agar disc with fungi isolate. For control, agar disc Ganoderma were inoculated without endophyte
microbes. All of the antagonistic were conducted triplicate and incubated in 28
o
C. The ability of the
endophyte microbes to inhibit the growth of G. boninense was determined after 7 days incubation
by measuring the diameter of the G. boninense colony in control plate (R1) compare with the
diameter of the G. boninense colony in plate with endophyte microbe (R2).
Chitinolytic activity assay. Bacteria and fungi isolates were inoculated to liquid chitin
medium with 0.3 % chitin (w/v) and incubated at 37
o
C with orbital shaking 150 rpm. The chitinolytic
assay was measured after 1, 2, 3, 4, 5, 6, and 7 days after incubation using Spektrophotometer UV-
Vis at 420 nm. One unit of chitinase was represented as nmol N-acetylglucosamine min
-1
mL
-1

protein. N-acetylglucosamine was used as a standard with variation concentration 0-200 ppm.

Identification of endophyte microbes
Isolation 16s rRNA gene for bacteria and ITS rRNA gene for fungi. Single colony of 24
hours bacteria from NA was inoculated to 5 mL Luria Broth (LB) and incubated for 18 hours at 37
o
C
with orbital shaking 150 rpm. The culture was centrifuged at 6000 rpm for 5 min. The pellet was
used for the isolation of DNA using Wizard Genomic (Promega) by manufacture procedure. One of
5-day-old fungi colony from PDA was inoculated into 25 mL Potato Dextrose Broth (PDB) and
incubated for 5 days at room temperature. The mycelium was used for the isolation DNA using
Plant Genomic DNA (Sigma) following the manufactures procedure. The 1500 bp of 16S rRNA
th
gene for bacteria was amplified using 9F (GAG TTT GAT CCT GGC TCA G) and 1510R (GGT TAC
CTT GTT ACG ACT T) primers and 600 bp of ITS rRNA gene for fungi was amplified using ITS 1
(TCC GTA GGT GAA CCT GCG G) and ITS 4 (TCC TCC GCT TAT TGA TAT GC) primers.
Polymerase chain reaction was carried out in a thermal cycler (Applied Bio system Verity) in a total
volume of 50 uL containing 2.5 mM MgCl2, 5uL of 10X Taq Buffer, 200 mM dNTPs, 50 pmoles of
each forward and reverse primer, Dream Taq Polymerase (Fermentas), and 10 ng DNA template.
PCR was performed by initial denaturation at 95
o
C for 4 min, followed by 35 cycles of denaturation
at 95
o
C for 1 min, annealing at 55
o
C for 1 min, extension at 72
o
C for 1 min, with final extension at
72
o
C for 10 min.
Cloning and transformation. Escherichia coli DH5 cells were transformed with PCR-
amplified 16S rRNA genes and ITS rDNA genes ligated in pGEM easy vector plasmid (Promega)
using Fermentas DNA ligation kit (Fermentas). The plasmid was transformed to E. coli DH5 using
heat shock treatment. The transformed cells (100 uL) were spread on LA plates containing X-Gal
(50 ug/ml), IPTG (100 ug/ml) and ampicillin (50 ug/ml). The plates were incubated at 37
o
C for 16
hours to screen blue and white colonies. Positive result was confirmed by PCR using M13F and
M13R primers of white colonies.
Gene sequencing. The 16s rRNA and ITS rRNA gene was sequenced to determine the
homology with the known sequences in the NCBI database. DNA sequencing was done on
FirstBase using M13 forward sequencing primer (GTAAAACGACGGCCAGT).


Seventeen of endophyte bacterias were isolated from oil palm root with chitinolytic index
ranged from 1.00 to 3.43 (data not showed). The ability of bacteria to form clear zones was
measured qualitatively through chitinase activity of bacteria. The chitinase enzymes produced by
bacteria are able to diffuse to the media. It can be seen from the presence of clear zones on the
media. Most of the bacteria are Gram-negative (66%). According to Bell et al.,(1995), the
abundance of Gram-negative endophytic bacteria in the oil palm roots was supported by population
endophytes in other plant
Endophyte fungi of T1 and T13 isolates sp. are white color colony and scattered greenish
patches become visible as the conidia are formed (Figure 1A). Microscopic of T1 and T13 isolates
showed that the hyphae are septate and hyaline. Phialides are branched, flask-shaped, and
attached to the conidiophores. Conidia have round or ellipsoidal form and have green color with 3
m average diameter (Figure 1E). V2 and V3 isolates have white colony form in PDA initially, but
typically become green (Figure 1B). Phialides are branched and tapered at tips. Spherical conidia
gathered at tip of phialides in a tight, and ball-shaped (Figure 1F). A1 and A2 isolates have varies
colony color from black to pale (Figure 1C). A1 and A2 isolate showed that hyphae are septate and
hyaline. Conidiophores arise from the basal foot cell found at the supporting hyphae and terminate
in a vesicle at the tip (Figure 1G). Mycelium morphology of F1 and F2 isolates are mostly white, but
sometimes can be purple (Figure 1D). Some species also produce distinctly different conidia in the
aerial mycelium (referred to as microconidia). Aerial mycelium is the growth of hyphae above the
agar surface and often form a convex shape (Figure 1H).
th

(A,E: T1 and T3 isolates; B,F: V2 and V3 isolates; C,G: A1 and A2 isolates; D, H: F1 and F2 isolates)

Figure 1. Morphological and histological of fungal endophytes.

Antagonistic test was used to measure the ability of bacteria in inhibiting the growth of
Ganoderma in vitro. Inhibition ratio of bacteria and fungi against G. boninese has different ranges.
For bacteria, B2.1.2 isolate has the highest inhibition ratio (67%), while B24.1.7 and B28.5.3 isolate
has the lowest inhibition ratio (26 %) and V3 isolate has the highest inhibition ratio (64 %) while the
F2 has the lowest inhibition ratio (33 %) (Table 1). There are two possible mechanisms to inhibit
growth of G. boninense, both are antifungal compound and chitinase activity. The chitinase could
lysis cell wall of G. boninense. In addition, bacteria and fungi also capable to produce secondary
metabolites, these can inhibit the growth of pathogenic fungi. According to Sidduqque et al., (2009),
Trichoderma can produce volatile compounds with marked gas formation and capable to inhibit the
growth of G. boninense up to 70% by dual culture method . A compound produced by Trichoderma
is known as 6 - pentyl-alpha-pyrone (6PAP) which is a secondary metabolites compound (Coney et
al. 1997).

Table 1 Antagonistic potential of endophyte microbe in dual culture test

Means in the same column with different alphabet(s) are significantly different (p < 0.05) according to Duncan test.

Microbe isolate Inhibition ratio (%)
a. Bacteria
B2.1.2 67 a
B93.22.83 37 b
B28.5.3 26 d
B50.1.3 34 c
B24.1.7 26 d
B13.10.4 34 c
b. Fungi
T1

58 b
T13 61 ab
V2 63 a
V3 64 a
A1 45 c
A1 37 d
F1 38 cd
F2 33 d
th
All microbe isolates could produce chitinase enzyme activity although with different pattern
(Table 2). B13.10.4 isolate of bacteria has the highest chitinase activity (3.43 U/mL at 5 days of
incubation).Whilst, the highest enzyme activity of chitinase in fungi was T1 isolate (2.07 U /mL at 7
days of incubation). Although B2.1.2 and V3 isolates have the highest inhibition ratio, they did not
produce enzyme with highest activity. According to Aktuganov (2003), chitinase activity was not
related to antifungal activity. The bacteria with high antagonist activity is not always have a high
chitinase activity.
Synergism between the antifungal compounds and enzymes of bacteria can enhance the
role of bacteria as bio-control pathogen (Sheri et al., 2002). Some studies suggest that the enzyme
chitinase production of the genus Trichoderma spp. is more effective than chitinase enzyme
produced by other organisms, to inhibit a various plant pathogenic fungi (Lorito et al., 1994).
Several studies are also reported that Trichoderma was capable in producing chitinase enzymes
that play a role in several fungal pathogens including Sclerotium rolfsii and Rhizoctonia solani,
(Haran et al., 1996; Harman et al., 1993).

Table 2 Chitinase activity enzyme from chitinolytic microbe

Means in the same column with different alphabet(s) are significantly different (p < 0.05) according to Duncan test.

Table 3 Identification of selected microbe based on ribosomal DNA

Isolate Identity Homology (%)
B2.1.2 Burkholderia sp 99
B93.22.83 Serratia sp 99
B24.1.7 Acinetobacter sp 99
B13.10.4 Bacillus cereus 99
T1 Trichoderma asperellum 99
V3 Hyphocrea virens 99
A1 Aspergillus sp 99
F1 Fusarium oxysporum 99

The fungi and bacteria were identified base on their ribosomal DNA. Identification of fungi
showed that there are Trichoderma, Hypocrea, Aspergillus, and Fusarium (Table 3). These four
fungi are known to be a natural bio-control of fungal pathogens (Krupke et al. 2003; Rubini et al.,
2005; Adriana & Sergio 2001). Identification of potential isolates showed that they are Serratia,
Microbe isolate Enzyme activity (U/mL) Time incubation (days)
a. Bacteria
B2.1.2 1.54 c 5
B93.22.83 1.51 c 6
B28.5.3 1.44 cd 7
B50.1.3 1.28 d 5
B24.1.7 2.08 b 2
B13.10.4 3.43 a 5
b. Fungi
T1 2.07 a 7
T13 1.75 b 6
V2 1.51 c 2
V3 1.16 de 2
A1 0.99 e 6
A2 0.93 e 6
F1 1.56 c 6
F2 1.30 d 6
th
Burkholderia, Acinetobacter, and Bacillus (Table 3). These results proved that several bacteria and
fungi are potential as bio-fungicide because of their high inhibition ratio and activity of chitinase.

References

Aktuganov GE, Melent'ev AL, Kuz'mina LY, Galimzyanova NF, and Shirokov AV. 2003.

The chitinolytic activity
of Bacillus Cohn bacteria antagonistic to phytopathogenic fungi. Microbiol 72(3): 313-317
Adriana O and Sergio O. 2001. In vitro evaluation of Trichoderma and Gliocladium antagonism against the
symbiotic fungus of the leaf-cutting and Atta cephalotes. Mycopathologia 150:53-60.
Bell CR, Dickie GA, Harvey GLW and Chan FYWJ. 1995. Endophytic bacteria in grapevine. Canadian J.
Microbiol., 41: 4653
Coney JM, Lauren DR, Poole PR, and Whitaker G. 1997. Microbial transformation of the Trichoderma metabolite
6-n pentyl-2H pyran-2- one. Nat. Prod. 60:1242-1244.
Darmono. 1996. Pendekatan bioteknologi untuk mengatasi masalah penyakit Busuk Pangkal Batang Kelapa
Sawit Akibat Serangan Ganoderma. Warta Puslit. Biotek Perkebunan. 1 : 17-25
Flood J, Bridge PD, and Holderness M. 2000. Ganoderma Diseases of Perennial Crops. CABI Publishing,
Wallingford. Uk 275 p
Haran S, Schickler H, Oppenheim A, and Chet I. 1996. Differential expression of Trichoderma harzianum
chitinases during mycoparasitism. Phytopathology 86:980-985.
Harman GE, Hayes CK, Lorito M, Broadway RM, Di Pietro A, Peterbauer C, and Tronsmo A. 1993. Chitinolytic
enzymes of Trichoderma harzianum: Purification of chitobiosidase and endochitinase. Phytopathology
83:313-318.
Jinantana J and Sariah M. 1997. Antagonistic effect of Malaysian isolates of Trichoderma harzianum and
Gliocladium Viren on Sclerotium rolfsii. Pertanika. J. Trop. Agric. Sci., 20: 3541
Krupke AO, Castle AJ, and Rinker DL. 2003. The North American mushroom competitor Trichoderma
aggressivum f. agrressivum, produces antifungal compounds in mushroom compost that inhibit mycelial
growth of the commercial mushroom Agaricus bisporus.Mycol. Res. 107:1467-1475.
Lorito M, Hayes CK, Zoina A, Scala F, Del Sorbo G, Woo SL and Harman GE. 1994. Potential of genes and
gene products from Trichoderma sp. and Gliocladium sp. for the development of biological pesticides.
Mol Biotechnol 2: 209-217.
Rubini MR, Silva-Ribeiro RT,Pomella AVW, Maki CS, Araujo WL, dos Santos DR, and Azedevo JL. 2005.
Diversity of endophytic fungal community of cacao (Theobroma cacao L.) and biological control of
Crinipellis perniciosa, causal agent of witches broom disease. Int. J of Bio Sc. 1: 24-33
Sapak Z, Meon S and Ahmad ZAM . 2008. Effect of endophytic bacteria on growth and suppression of
Ganoderma infection in oil palm. Int. J. Agri. Biol 10 (2) :127-132
Sheri W, Vincenzo F, Felice S, and Matteo L. 2002 .Synergism between fungal enzymes and bacterial
antibiotics may enhance biocontrol.Antonie van Leeuwenhoek 81(4) :353-356
Shiomi HF, Harllen SAS, Itamar SDM, Flavia VN, and Wagner B. 2006. Bioprospecting endophytic bacteria for
biological control of coffee leaf rust (Piracicaba, Brazil.) J SciAgri , 63 (1):32-39.
Siddiquee S, Umi Kalsom Yusuf, Hossain K, and Japan S. 2009. In vitro studies on the potential Trichoderma
harzianum for antagonistic properties against Ganoderma boninense. International Journal Food,
Agriculture, and Enviroment 7(2): 970-976.

th
Chitinase Activities of Oil Palm Root at Early Infection of
Arbuscular Mycorrhizal Fungi

Happy Widiastuti

Indonesian Biotechnology Research Institute for Estate Crops
Jl Taman Kencana No. 1 Bogor, Indonesia 16151
Corresponding author: [email protected]

Abstract

The activity of chitinase of oil palm root at the early of arbuscular mycorrhizal fungi (AMF) colonisation was
studied. The results showed that early in colonisation (0-5 weeks), chitinase activity in roots increased
nevertheless eventually suppressing occurs 5-8 weeks after inoculation. Inhibition of chitinase activity is
influenced by AMF species and fertilization. Suppression of endochitinase activity of effective species is higher
than the species that are less effective, especially in the fertilization treatment. The activity of exochitinase was
depressed in the presence of AMF colonisation. In the treatment without fertilizer, suppression of exochitinase
activity of inoculated roots with G. margarita is higher than those inoculated with A. tuberculata. Inhibition of
chitinase activities on secondary roots that occurs at the inoculation of G. margarita is higher than those
inoculated with A. tuberculata and vice versa in the primary root.

Keywords: chitinase activities, palm oil, early colonisation, arbuscular mycorrhizal fungi

Introduction

Arbuscular mycorrhizal fungi (AMF) is a fungus symbioses with the oil palm. Biochemical
processes involved in plant symbiosis with fungi has been studied. Differences in proteins both
quantitatively and qualitatively has been shown between AMF inoculated and uninoculated plants.
AMF colonization seems to be in place for increasing the size of low protein expression as shown in
tobacco (Dumas et al, 1996). The emphasis is more consistent in the chitinase activity which is also
have a role in defense plants in the early stages of AMF colonisation. Penetration of AMF in root
involves a series of changes in morphology and physiology in plants and fungi. However, as occurs
in plant-pathogen interaction mechanisms of induction and suppression associated with plant
defense is the key to the colonization of AMF and its compatibility with the host plant (Garcia-
Garrido & Ocampo, 2002).
The effectiveness of plant defense responses associated with the speed of the process of
introduction of specific signaling molecules called elisitor. Elisitor can be secreted by the microbes
that infect or as a result of breakdown of plant cell walls. Regulatory mechanisms of defense
responses through degradation of the molecule can be issued elisitor AMF for example by
hydrolysis enzymes such as chitinase, glucanase B 1.3, kitosanase. Lambais and Mehdy (1996)
observed a suppression of activity endochitinase up to nearly twice in the AMF inoculation
treatment and the level of infection-suppressing this enzyme was higher in the effective strain AMF
compared to strains that are less effective. This research aim was to study plant defense responses
during early colonisation, especially AMF chitinase activity.


Planting materials used were germinated oil palm from IOPRI Medan. Germinated oil palm
was grown in sterile sand until the age of 3 months. AMF inoculation on the palm was made by the
th
method of pre-nursery i.e by developing AMF colonization in P phaseoloides prior to colonisation to
oil palm seedling. P. phaseoloides grown in polybags 50 x 50 cm in sized without holes containing
10 kg of sterilized Cikopomayak acid soils. Inoculum dose and optimum dose of fertilizer was based
on the optimization experiment (Widiastuti et al, 2002). Plants were maintained in a greenhouse by
watering with cooling boiled water. Harvesting was done at weeks 0, 3, 5, 8, and 11 after inoculation
by washing the roots with water taps. Observations were conducted on fresh and dry weight of
seedlings, chitinase activitieas (Lambais & Mehdy, 1996), and the percentage of AMF colonisation.
Chitinase activity was determined by counting the hydrolyzed N acetyl glucosamine using BSA as
protein standard. The two factors tested were AMF species (without AMF, A. tuberculata, and G.
margarita) and fertilizing (without and with fertilizer). The inorganic fertilizer dose of control was
based on Lubis (1992). Experimental design used was completely randomized group design with
factorial pattern.


AM fungi colonisation in oil palm root
Chemical analysis showed that the soil was very acid (pH H
2
O 3.8), the content of C, N,
P
2
O
5
, K
2
O, CaO, MgO were very low at 1.59; 0.097; 0.013; 0.01; 0.066; 0.054% and 16.23 Aldd me
100 g
-1
respectively. Colonisation of AMF began weeks after inoculation in both the primary and
secondary roots. However, colonisation in secondary roots was higher than those in primary roots.
Moreover, colonisation of AM fungi in no fertilization treatment was higher than those both A.
tuberculata and G. margarita (Fig 1).

Figure 1. Percentage of AMF colonisation in primary (left) and secondary (right) oil palm roots.

Chitinase activity in the primary root
The analysis showed that in the primary roots which were not inoculated with AMF, the
activity of exochitinase was higher compared to those of the inoculated one. Exochitinase activity
increased until the fifth week after inoculation and subsequent declined at week eight and very low
at week 11. These results indicated that the exochitinase activity was temporary and there is
emphasis of exochitinase activities particularly began 8 weeks after AMF inoculation. The effect of
fertilization showed a trend that in palm roots without AMF inoculation and inoculated with G.
margarita, fertilization causes the higher activity of exochitinase compared to those not fertilized.
However, these results differed with exochitinase activity of palm roots inoculated with A.
tuberculata. The exochitinase activities of the root that are not fertilized, is higher compare to those
fertilized. Emphasis of the exochitinase activity in the inoculated roots of palm inoculated with A.
tuberculata both at without fertilization and fertilized was higher than the activity exochitinase palm
roots inoculated with G. margarita.These results indicate that in the primary root, the activity of
exochitinase influenced by AMF species and the presence of fertilization.
0
5
10
15
20
25
30
35
40
0 3 5 8 11
AtP0
AtP1
GmP0
GmP1
0
2
4
6
8
10
12
14
16
18
0 3 5 8 11
AtP0
AtP1
GmP0
Weeks after inoculation Weeks after inoculation
P
e
r
c
e
n
t
a
g
e

o
f

i
n
f
e
c
t
i
o
n

P
e
r
c
e
n
t
a
g
e

o
f

i
n
f
e
c
t
i
o
n

th
Endochitinase activity was lower in primary roots compared to exochitinase activity.
Endochitinase activity in primary roots that not inoculated with AMF was higher compared to those
inoculated. Unlike to the exochitinase activity, the peak of endochitinase acitivity occurred at week 5
and declined until week 8. Activity of endochitinase of oil palm root unfertilized inoculated with A.
tuberculata is higher than those of inoculated with G. margarita. This result was in line with
exochitinase activity (Fig. 2). With the application of fertilizer, the activity endochitinase of primary
palm root inoculated with G. margarita was higher than those of the inoculated with A. tuberculata.
These results indicated that the dose of fertilizer and type of AMF affect endochitinase activity on
secondary roots.
The data of chitinase activity in general, showed that in the primary root chitinase activity
of oil palm uninoculated with AMF was higher than those of inoculated with AMF. This trend
happened in the oil palm root inoculated with G. margarita, but the opposite occurred in oil palm
roots inoculated with A. tuberculata.

Figure 2. Exochitinase activity (A), endochitinase (B), and total chitinase (C) of primary oil palm roots in
response to treatment.

Chitinase activity in the secondary roots
Exochitinase activity on the secondary roots of palm oil was much higher compared with
exochitinase activity in the primary root. This difference reached 10 times. Endochitinase activity in
oil palm roots without AMF inoculation was higher than those of inoculated with AMF. In the
secondary roots inoculated with A. tuberculata, endochitinase activity without fertilization was higher
than those fertilized root. These results are similar to those in primary roots. But for oil palm roots
th
inoculated with G. margarita, there was no difference of exochitinase activity between a fertilized
and unfertilized. In addition, it was shown that in fertilization oil palm root, the emphasis of chitinase
activity was slower compared to those of without fertilized.
Activity of endochitinase of secondary roots of palm was lower than exochitinase activity
on the same root. In addition, endochitinase activities of palm root that were not inoculated was
higher compared to those inoculated with the AMF. In secondary oil palm roots inoculated with A.
tuberculata but unfertilized, endochitinase had a higher activity compared with those of fertilized, but
in contrary to the roots of oil palm inoculated with G. margarita. These results were similar to those
observed in primary roots. At the root of the fertilized palm, the activity of the endochitinase the
activity of root inoculated with G. margarita was higher compared to those inoculated with A.
tuberculata, whereas the opposite occured in the treatment without fertilization. These results were
in line with that occured in the primary root. The high of endochitinase activity in roots inoculated
with A. tuberculata followed by a higher emphasis anyway.
General description for chitinase activity in the secondary roots of palm oil showed that the
activity of chitinase in the palm oil root that were not inoculated with AMF was higher than that
inoculated with AMF (Fig 3.). In oil palm inoculated with A. tuberculata, fertilization actually
decreased the activity of chitinase in secondary roots. While palm oil inoculated with G. margarita,
there was no difference between a fertilized and unfertilized.

0
500
1000
1500
2000
2500
0 3 5 8 11
E
x
o
c
h
i
t
i
n
a
s
e

a
c
t
i
v
i
t
y

n
m
o
l

e
q

N

a
c
e
t
y
l

G
l
u

m
g
-
1
h
-
1
Week after inoculation
M0P0
M0P1
AtP0
AtP1
GmP0
GmP1
A

Figure 3. Activity of exochitinase (A), endochitinase (B), and total chitinase (C) of secondary oil palm roots in
response to treatment.
th
Possible differences in plant response to AMF colonisation in particular is evident from the
activity of chitinase can be a bookmark for the selection of the effectiveness of AMF. In the present
study demonstrated that inoculation suppressed the activity of chitinase. Suppression level was
influenced by the AMF species and doseage of fertilizer. Emphasis on treatment without fertilization
was highest in week 3 after inoculation, while the emphasis of chitinase activity on fertilization
treatment was observed 5 weeks after inoculation. Fertilization appears to slow the emphasis of
chitinase activity.
The same is true of the exochitinase activity are fertilized palm that inoculated with G.
margarita. Despite this emphasis on endochitinase activity of G. margarita inoculation lower
compared to those inoculated with A. tuberculata. Total chitinase activity in the secondary roots
either by fertilization or without fertilization showed that the inoculation of G. margarita more
suppresse than thoses the inoculation with A. tuberculata.
Changes in isoenzyme patterns and biochemical properties of several enzymes associated
with plant defense as chitinase has been shown for tomato root colonization by AMF (Pozo et al.,
1996) with the induction of new isoforms. These hydrolytic enzymes act as a defense against
pathogen attack because of its potential hydrolyze fungal cell wall polysaccharides (Pozo et al.,
1996). Induction of this enzyme activity in AMF symbiosis may also be involved in the protection of
plants against pathogenic fungi (Dumas-Gaudot et al., 1996).
The present study indicated that there was an emphasis on the chitinase activity which
was influenced by inoculation with AMF, AMF species, and fertilization. Fertilization slow emphasis
chitinase activity. In addition, the data showed generally lower total chitinase activity in the presence
of fertilization compared with those not fertilized, especially in the inoculation with A. tuberculata.
While at the inoculation with G. margarita fertilization increased the chitinase activity. The same
thing also happened in controls. The results in this study seemed in line with Blee & Anderson
(1996) suggested that P can regulate plant defense responses. The results suggested that
fertilization decreased 1.3 glucanase (occurs with mRNA). The delay of suppression of chitinase
activity supposed to be caused by the slow of AMF colonisation in the presence of fertilization.
Emphasis on fertilization treatment to endochitinase activity in roots inoculated with A.
tuberculata is higher than those on inoculated roots of G. margarita and vice versa in the treatment
without fertilizer. In a previous study demonstrated that A. tuberculata is more effective in improving
growth and P uptake of oil palm seedlings in comparison with G. margarita (Widiastuti et al, 2002).
In addition Widiastuti et al (2005) showed that the optimum dose of inorganic fertilizer of oil palm
inoculated with G. margarita was higer compared to those inoculatred with A. tuberculata. These
results suggest that suppression of effective species to endochitinase activity is higher than those to
species that are less effective, especially in the fertilization treatment. Similar to Lambais & Mehdy
(1996) the effective strain is more pressing AMF endochitinase activity compared to those that are
less effective. However this only occurs at an optimal symbiosis is the application of fertilizer, while
the treatment without fertilization occurs the opposite of the less effective strain is more pressing
endochitinase activity compared to effective strain.
In this study exochitinase depressed activity in the presence of AMF colonisation,
however, there were differences in emphasis between the root level of the inoculated A. tuberculata
and G. margarita. In the treatment without fertilizer, suppression activity of inoculated roots
exochitinase of G. margarita was higher than A. tuberculata. While the result of fertilizer there was a
difference in primary and secondary roots. The emphasis on secondary roots that occurs at the
inoculation G. margarita was higher than A. tuberculata and vice versa in the primary root. These
results indicate that in the less effective strain, the emphasis on exochitinase activity higher
compared to the effective strains, especially on secondary roots. These results were different from
those expressed Lambais and Mehdy (1996) who reported increased activity exochitinase up to 3
times the effective strain AMF. In this study exochitinase suppression activities occured on the
effective strain is lower than those that are less effective. The results of this study indicated that
th
plants respond differently to AMF colonisation compared to pathogen infection. The mycorrhizal
plant has a defense mechanism that temporally and very weak in contrast to pathogen.

References

Blee KA, AJ Anderson. 1996. Defence-related transcript accumulation in Phaseolus vulgaris L. colonized by the
arbuscular mycorrhizal fungus Glomus intraradices, Schenck & Smith. Plant Physiol. 110, 675-688.
Dumas-Gaudot, ES Slezack, B Dassi, MJ Pozo, V Gianinazzi-Pearson, and S Gianinazzi. 1996. Plant hydrolytic
enzymes (chitinases and -1,3-glucanases) in root reactions to pathogenic and symbiotic
microorganisms. Plant and Soil. 185, 211-221.
Garcia-Garrido, JM, and JA Ocampo. 2002. Regulation of the plant defence response in arbuscular mycorrhizal
symbiosis. J. Exp. Bot. 53, 1377-1386.
Lambais MR, and MC Mehdy. 1996. Soybean roots infected by Glomus intraradices strains differing in infectivity
exhibit differential chitinase and -1,3-glucanase expression. New Phytol. 134, 531-538.
Lubis AU. 1992. Kelapa Sawit (Elaeis guineensis Jacq) di Indonesia. Pusat Penelitian Perkebunan Marihat
Bandar Kuala. Pematang Siantar. Sumatera Utara.
Pozo, MJ, E Dumas-Gaudot, S Slezack, C Cordier, A. Asselin, V Gianinazzi-Pearson, C Azcon-Aguilar and JM
Barea. 1996. Detection of new chitinase isoforms in arbuscular mycorrhizal tomato roots: possible
implications in protection against Phytophthora nicotianae var. parasitica. Agronomie, 16, 689-697.
Widiastuti, H. E. Guhardja, N. Soekarno, L. K. Darusman, D. H. Goenadi and S. Smith. 2002. Optimasi
simbiosis cendawan mikoriza arbuskula Acaulospora tuberculata dan Gigaspora margarita pada bibit
kelapa sawit di tanah masam. Menara Perkebunan 70, 54-62.

th
In vitro Test of Rhizosphere Chitinolytic Bacteria as a Biocontrol
for Ganoderma boninense

Rika Fithri Buana
*
, Wisnu Adi Wicaksono, Elizabeth C. Situmorang

Plant Production and Biotechnology Division, PT SMART Tbk, Bogor, Indonesia
* Corresponding author: Plant Production and Biotechnology Division, PT SMART tbk
Jl. Padjajaran Raya No. 78F-G, Bogor, Indonesia
Tel.: +62 251 831 0854; fax: +62 251 831 0854.
[email protected]

Abstract

G. boninense is a fungal pathogen that causes basal stem rot in oil palm (Elaeis guineensis). Chitinolytic
bacteria are abundant in soil and well known as a natural biocontrol of fungal pathogen. The objective of this
research is to obtain rhizosphere chitinolytic bacteria as a candidate of biocontrol agent for G. boninense.
Nineteen indigenous bacteria from Padang Halaban Estate, North Sumatera, were tested for their antagonistic
properties against G. boninense by in vitro dual culture on PDA plates. Their chitinolytic activities were tested
using colloidal chitin as the substrate. Chitinase activity was determined colorimetrically by detecting the amount
of N-acetylglucosamine released from colloidal chitin substrate. Crude enzyme secreted by the bacteria were
characterized by SDS-PAGE with chitinase from Trichoderma as a control. Six of the isolates have an inhibition
activity against G. boninense growth with B3.4 showed the highest percentage inhibition ratio growth or PIRG
(58.75%). Inhibition of G. boninense growth in vitro might due to a competition for nutrients or other antifungal
compound from certain bacteria which diffuses in the agar. B3.2 showed the highest activity of chitinase (10.44
U/mL), but B3.4 has lower activity of chitinase (7.08 U/mL). It can be assumed from the result that PIRG does
not have correlation with the activity of chitinase. The results of enzyme characterization showed that B3.3, B3.2
and B3.4 has a molecular mass of 37kDA, which is a similar molecular mass with chitinase from Trichoderma
viridae

Keywords: rhizosphere bacteria, Ganoderma boninense, Elaeis guineensis, chitinase

Introduction

Basal stem rot disease (BSR) caused by Ganoderma boninense is currently a major
disease in oil palm plantations (Darmono, 1998). The disease can destroy up to 80% of the stand
palms by the time when the palms are halfway through their normal economic life span (Idris, 2003).
Ganoderma boninense is a saprophytic fungus activated by favorable conditions to behave
parasitically (Statmets, 2004). Like all fungi, it has no chlorophyll and thus, lack photosynthetic
capability. Instead of manufacturing their own food, fungi absorb nutrients from either living or dead
host tissue (Haniff, 2005). the fungus typically attack already weakened oil palm as Ganoderma
seldom seriously infects undamaged trees (Paterson, 2007). The effects of Ganoderma infection on
productivity decline in palm crops have been concerned since replanting of oil palm land was began
in South-East Asia, especially in Malaysia and Indonesia (Turner, 2003).
BSR has been an endemic disease found in PT. SMART Tbk. oil palm plantation
especially in Padang Halaban, North Sumatera, Indonesia. Biological control of pathogenic fungi
provides an attractive and alternative management for fungal diseases without the negative impact
of synthetic antifungal agents that can cause environmental pollution and may induce pathogen
resistance (Haas & Dfago, 2005). Plant disease control by chitinolytic bacteria has long been
reported (Sneh, 1981). Several strains of bacteria, such as Aeromonas caviae, Bacillus sp., Serratia
plymuthica, and Enterobacter agglomerans are well-known chitinolytic bacteria (Das et al., 2010).
Some Trichoderma sp. have been described as biological control agents against fungal pathogens
and widely used as biocontrol because of its mycoparasitic activity (De La Cruz, 1992). Chitinolytic
th
enzymes have been considered as an important factor to control soilborne pathogens because of
their ability to degrade fungal cell walls, of which a major component is chitin (Chet, 1987).
Chitin is widely available in the soil derived from the decay and degradation of dead cells,
so that some bacteria that live on the ground are good in degrading chitin (Suryanto et al., 2005).
The aim of this study was to isolate chitinolytic bacteria from rhizosphere soils in Padang Halaban
estate and to screen their antagonistic activity against G. boninense.


Isolation of bacteria
Rhizospheric soil were collected near the root of the uninfected plant in endemic site of G.
boninense. Suspension were made by adding 10 g of soil to 100 mL sterile basic salt solution
(0.85% NaCl). Ten fold serial dilutions of these suspensions were made and plated on Nutrient
Agar (NA). The colony were selected and purified with 4-way streak method on NA.

Dual-culture technique
Dual culture were made to obtain the percentage inhibition of radial growth (PIRG) of G.
boninense (Bivi, 2010). Potato Dextrose Agar (PDA) was poured onto 9 cm diameter Petri dishes.
Isolated bacteria was streaked into the PDA plate 2.5 cm from the edge of Petri dish. A 5 mm agar
disc cut from the side of an actively growing pure culture of 5-day old G. boninense placed 2.5 cm
from the edge at the opposite side of the same Petri dish. For the control plate, only G. boninense
was placed in a similar manner without bacteria on a fresh Petri dish. The experiment was made in
three replication each bacteria. The plates were incubated at 28
o
C for five days. Results revealed
as mean colony growth of the causal pathogen in the presence of the bacteria and its growth on the
control plate (without the bacteria). The outcome of two readings was calculated into the formula for
the PIRG as below :

% PIRG = R1 - R2 X 100
R1
Where, PIRG = percentage inhibition of radial growth; R1 = radial growth of G. boninense in the
absence of bacteria (control); R2 = radial growth of G. boninense in the presence of bacteria.

Chitinase assay
Chitinase activity was determined colorimetrically by detecting the amount of N-
acetylglucosamine (GlcNAc) released from a colloidal chitin substrate (Reissig, 1955). Selected
isolates were inoculated into 100 ml of 10% chitin medium and incubated at 37
o
C on rotary shaker
120 rpm for 5 days. Flask were removed every 24 hours and pipetted 10 mL from each mixture
were filtered through filter paper. The filtrate as a crude enzyme were pipetted 1.5 ml into 0.75 ml
phosphate buffer and 1.5 ml of 0.3% coloidal chitin in 15 ml Corning centrifuge tube. The reaction
mixture were incubated in 37
o
C for 30 min, and centrifuge the mixture to separate the product from
the remaining substrate. Pipetted 2.5 ml supernatant into 5 ml Schales reagent and 2.5 ml distilled
water. The mixture was boiled for 10 min to stop the reaction of the remain enzyme. The reaction
was measured with spectrophotometer at 420 nm. N-acetylglucosamine was used as a standard.
One unit of chitinase acivity was defined as the amount of enzyme that released 1 mol GlcNAc or
its equivalent from colloidal chitin in 1 min (Zilda, 2006).

Protein characterization
Crude enzyme secreted by the bacteria were characterized by sodium dodecyl sulfate
(SDS)-polyacrylamide gel electrophoresis (PAGE) with 12 % separator gel and 4% stacking gel.
Crude supernatants protein were mixed with 2x sample buffer (1:1), boiled for 4 min, then load. The
th
gel were stained with 0,1% Coomassie brilliant blue R-250, and destained with 10% acetic acid and
20% methanol.


There are 19 indigenous bacteria isolated from rhizosphere soil in Padang Halaban.
Screening of biocontrol bacteria was carried out by dual culture. It showed that six of them have an
inhibitory activity against G. boninense growth (Table.1). B3.4 showed the highest PIRG of G.
boninense amongs other isolates, it showed 58.75% and the B3.3 is the lowest (12.20%). The
inhibition of G. boninense growth might due to the presence of chitinase or other anti-fungal
properties produced by the certain bacteria. Many publications have reported that soil bacterias are
capable in producing anti-fungal metabolites properties that inhibited mycelia growth of
phytopathogen fungi (Fernando & Linderman,1994; Sisler, 1969; Yiu-Kwok et al., 2003). Many of
the anti-fungal properties affect the physiological activities of pathogenic fungi (Vesperman, 2007).

Table 1. Antagonistic potential of soil bacteria in dual culture test

Bacterial isolates PIRG (%)
B3.3 12.20 d
B14.1 35.56 b
B3.1.1 22.22 c
B3.4 58.75 a
B11.2 31.11 b
B3.2 16.67 d
Mean in the same coloumn with different alphabet(s) are significantly different (P<0.05) according to DMRT

Bacteria B3.2 showed the highest activity of chitinase (10.44 U/mL) and the lowest was
B14.1 (7.08 U/mL) on day four of incubation. The result revealed that PIRG has no correlation with
chitinase activity. Bacteria with the highest PIRG (B3.4) showed less chitinase activity than bacteria
with lowest PIRG (B3.3). This result is in accordance to Aktuganov (2003) statement that there is no
correlation between PIRG and the ability of bacteria in producing chitinase. It can be assumed that
other anti-fungal property was responsible for the inhibitory effect in dual-culture of B14.1.

Table 2. Chitinase activity enzyme from isolated bacteria

Bacterial isolates Enzyme activity (U/mL)
Incubation time
(Days)
B3.2 10.44 a 4
B3.3 8.43 b 4
B3.4 9.94 a 4
B14.1 7.08 c 4
B3.1.1 8.37 b 4
B3.2.2 8.31 b 4
Mean in the same coloumn with different alphabet(s) are significantly different (P<0.05) according to DMRT.

Crude supernatan protein secreted by six bacterial isolates were characterized. Chitinase
from Trichoderma viridae were used as a control. The results revealed that the six isolates have
different banding pattern as shown in Figure 1. Chitinase from Trichoderma has a molecular mass
of 37 kDA (De Marco, 200), and most of chitinases have molecular mass of between 28 kDA - 43
kDA (Nielsen, 1997). Result showed that B3.2, B3.3, and 3.4 have a similar band between 30 kDA
40 kDA, in a range with most of chitinases molecular mass. The three other isolates showed a
th
similar band of 50 kDA. Singh et al, (1998) reported that chitinase from Paenibacillus sp. has
molecular mass around 50 kDA.

First lane represent the control of chitinase from Trichoderma viridae; Lane 1, B3.2; Lane 2, B3.3; Lane 3, B3.4; Lane 4, B14.1;
Lane 5, B3.1.1; Lane 6, B3.2.2; Lane 7, negative control.

Figure 1. SDS-PAGE analysis of total supernatan protein of isolates, stained with comassie brilliant blue.

The result showed that B3.2 was the best rhizosphere chitinolytic bacteria. The most
promising bacteria is B3.4. It is because bacteria with more 50% PIRG can be used as bio control
(Bivi, 2010). Synergism between chitinolytic and antagonistic bacteria could enhance the role of
bacteria as biocontrol pathogen. Combination of these two bacteria can be use as a biocontrol
candidate.

References

Aktuganov GE, Melent'ev AI, Kuz'mina LY, Galimzyanova NF, and Shirokov AV. 2003. The chitinolytic activity of
Bacillus Cohn bacteria antagonistic to phytopathogenic fungi. Microbiol 72(3): 313-317
Bivi MR, Farhana SN, Khairulmazmi A, and Idris A. 2010. Control of Ganoderma boninense: a causal agent of
basal stem rot disease in oil palm with endophyte bacteria in vitro. Int. J. Agric. Biol. 12(6): 1560-8530
Chernin L, Ismailov Z, Haran S, and Chet I. 1995. Chitinolytic Enterobacter agglomerans antagonistic to fungal
plant pathogens. App. Environ. Microbiol :1720-1726.
Chet I. 1987.TrichodermaApplication, mode of action, and potential as a biocontrol agent of soilborne plant
pathogenic fungi. Pages 37-160 in: Innovative Approaches to Plant Disease Control. I. Chet, ed. John
Wiley & Sons, New York.
De La Cruz J, Hidalgo-Gallego A, Lora JM, Benitez T, Pintor-Toro JA, and Llobell A. 1992. Isolation and
characterization of three chitinases from Trichoderma harzianum. Eur. J. Biochem 206: 859-867.
De Marco JL, Lima LHC, De Souse MV, and Felix CR. 2000. A Trichoderma harzianum chitinase destroys the
cell wall of the phytopathogen Criniprllis perniciosa : the causal agent of witches broom disease of
cocoa. W. J. Microbio. Biotechnol 16(4): 383-386.
Darmono TW.1998. Ganoderma in oil palm in Indonesia: current status and prospective use of antibodies for
the detection of infection. In: Harman GE, Kubicek CP, eds. Trichoderma and Gliocladium Volume 1:
Enzymes, biological control and commercial applications. UK: Taylor & Francis Ltd., 1998: 393.
Das SN, Sarma PV, Neeraja C, Malati N, and Podile AR. 2010. Members of Gammaproteobacteria and Bacilli
represent the culturable diversity of chitinolytic bacteria in chitin-enriched soils. W. J. Microbiol.
Biotechnol. 26: 1875-1881.
Fernando WGD and Linderman R. 1994. Inhibition of Phytophthora vignae and root rot of cowpea by soil
bacteria. Biological Agriculture and Horticulture 12: 1-14.
Haas D and Dfago G. 2005. Biological control of soil-borne pathogens by fluorescent pseudomonads. Nat.
Rev. Microbiol. 3: 307-319.
Haniff MH, Ismail S, and Idris AS. 2005. Gas exchange responses of oil palm to Ganoderma boninense
infection. Asian Journal of Plant Sciences 4 (4): 438-444.

kDA
150 --

60 -
50 --
37

30
25
20

th
Idris AS, Ismail S, Ariffin D, and Ahmad H. 2003. Control of Ganoderma-infected palm-development of pressure
injection and field applications. MPOB Information Series No. 131.
Nielsen KK, Nielsen JE, Madrid SM, and Mikaelsen JD. 1997. Characterization of a new antifungal binding
peptide from sugar beef leaves. Plant physiol, 113:83-91.
Paterson RRM. 2007. Ganoderma disease of oil palm- A white rot perspective necessary for integrated control.
Crop Protection 26 : 1369-1376
Reissig JL, Strominger JL, and Leloir LF. 1955. A modification colorimetric method for the estimation of N-
acetylamino sugars. J. Biol. Chem 27: 959-966.
Singh PP, Shin YC, Park CS, and Chung YR. 1998. Biological control of Fusarium wilt of cucumber by
chitinolytic bacteria. Phytopathology 89:92-99.
Sisler HD. 1969. Effect of fungicides on protein and nucleic acid synthesis. Ann. Rev. Phytopathol 7: 311-330.
Sneh B. 1981. Use of rhizosphere chitinolytic bacteria for biological control of Fusarium oxysporum f. sp. dianthi
in carnation. Phytopathol 100:251-256.
Stamets P. 2004. The role of mushrooms in nature. In: Elevitch C.R (Ed.). The overstory book: cultivating
connection with trees, 2nd Edn. permanent agriculture resource, USA., pp: 74-80.
Suryanto D, Munir E, and Yurnaliza, 2005. Eksplorasi Bakteri Kitinolitik : Keragaman Genetik Gen Penyandi
Kitinase pada Berbagai Jenis Bakteri dan Pemanfaatannya.Laporan Hasil Penelitian Hibah Bersaing
Perguruan Tinggi, Universitas Sumatera Utara, Medan.
Turner PD and Gillbanks RA. 2003. Oil palm cultivation and management. The Incorporated Society of Planters
Kuala Lumpur, Malaysia.
Vespermann AM, Kai, and Piechulla B. 2007. Rhizobacterial volatiles affect the growth of fungi and Arabidpsis
thaliana. Appl. Environ. Microbiol. 73: 5639-5641.
Yiu-Kwok C, Wayne A, McCormic K, and Keith AS. 2003. Characterization of antifungal soil bacterium and its
antagonistic activities against Fusarium species. Can. J. Microbiol., 49: 253-262.
Zilda DS, Fawzya YN, and Chasanah E. 2006. Karakterisasi enzim kitosanase dari bakteri kitinolitik T5a1 yang
diisolasi dari terasi. Jurnal pascapanen dan bioteknologi kelautan dan perikanan Vol. 1 No. 1.
Zaiton S, Sariah M, and Abidin Z., 2006. Isolation and Characterisation of Microbial Endophytes from Oil Palm
Roots : Implication as Biocontrol Agents against Ganoderma. Department of Plant Protection, Faculty of
Agriculture, Universiti Putra Malaysia, Selangor Darul Ehsan, Malaysia.

th
The Effect of Mulch, Trichoderma, and Arbuscular Mycorrhizal Fungi (AMF)
Biofertilizer on the Growth of Oil Palm Seedlings Inoculated with
Ganoderma

Happy Widiastuti

Indonesian Biotechnology Research Institute for Estate Crops
Jl Taman Kencana No 1 Bogor, 16151, Indonesia
Corresponding author: [email protected]

Abstract

A Greenhouse experiment was carried out to determine the effect of mulching, Trichoderma sp., Metharizium
anisopilae,. arbuscular mycorrhizal fungi (AMF) biofertilizer on the growth of oil palm seedlings. The experiment
was conducted in 70x80 cm sized of polybags filled with 50 kg of Latosol Ciomas soil. Mycorrhizal inoculum is in
the form of spores, hyphae and infected roots. Germinated oil palm was planted in polybag, then covered with
empty fruit bunches of oil palm (EFBOP) as mulch. The dose of inorganic fertilizer was 50% for the application of
AMF biofertilizer while on the other treatment the dose of fertilizer was 100%. The experimental design was
complete randomized design to test nine treatments: 1) without any fertilizer, 2) 100% inorganic fertilizer, 3)
EFBOP, 4) EFBOP+Trichoderma pseudokoningii+Trichoderma DT38, 5) EFBOP+T. pseudokoningii+
Trichoderma DT41, 6) EFBOP+T. pseudokoningii + Trichoderma DT38 + Metharizium anisopilae, 7) EFBOP+T.
pseudokoningii+Trichoderma DT41+Metharizium anisopilae, 8) EFBOP+T. pseudokoningii+Trichoderma DT38+
Metharizium anisopilae+AMF biofertilizer, 9) EFBOP+T. pseudokoningii+Trichoderma DT41+M. anisopilae+AMF
biofertilizer. The results showed that application of EFBOP as mulch enhanced the gowth of oil palm seedling
and combination with DT 41 and both T. pseudokoningii and Metharizium produce the similar growth with those
100% inorganic fertilizer treatment. While the addition of EFBOP+Trichoderma DT41+T. pesudokoningii
produced the highest seedling dry weight. The application of AMF biofertilizaer reduced the dose of inorganic
fertilizer yielded a similar seedling dry weight with those fertlized with 100% of inorganic fertilizer.

Key words: oil palm, mulch, empty fruit bunches oil palm, arbuscular mycorrhizal fungi, acid soil

Introduction

One method of organic matter application is to use it as mulch. Mulch is organic or
inorganic materials either natural or artificial which is placed above the soil and have a role to
protect and cover it. Some of the benefits of mulching is to minimize the occurrence of surface
runoff, increase water infiltration, protect the soil against rain, modify soil temperature, suppress
weeds, reduce the rate of dry surface soil, increase soil biological activity and modifies the level of
nutrient availability as well as to maintain or increase the availability of organic material soil (Baon,
1998). Basically the main function of mulching is to maintain the soil moisture. Water is a very
important factor in the cultivation of plants including crops. The application of mulch is not
accompanied with tillage practice. Muruganandam et al (2009) showed that the activity of enzymes
that play a role in N mineralization in no-tillage soil is significantly higher compared to conventionally
cultivated soil. While White & Rice (2009) suggested that the biological activity in no-tillage soil was
detected higher compared to conventional cultivated soil.
In the microbiological aspects, organic materials addition means the addition of carbon
and energy sources to improve microbe activities. The same thing seems to occur in peat soil.
Komariah et al (1993), Nurani et al. (2007) reported that the use of microbial consortia and EFBOP
increase soil pH and base saturation and lower CEC of peat soil as well as the C/N ratio. Microbes,
in addition to functioning release nutrients or nutrient mineralization in the process of decomposition
is also able to degrade toxic compounds (Sparling, 1998). However, microbe use root exudate as
th
source of carbon, energy and other nutrients to support their live. Brockling et al. (2008) suggests
that plants can regulate microbial communities through root exudates.
The application of inorganic fertilizer as well as pesticide in higher dose will disturb the
activities of soil microbes caused declining biological soil properties. These imbalances soil
properties affect the soil microbial communities to control soil borne pathogens and microbes that
play a role in the health of the land and crops. This is supported by research conducted by Vallad
et. al. (2003) which proves that the application of organic fertilizer (compost) reduce plant disease
attack. Rhizosfer manipulation seems necessary to maintain land productivity. Rousk et al (2009)
suggested that the decrease in pH will increase five times the population of fungi, and vice versa for
the bacteria. The aim of the research was to determine the effect of mulching, Trichoderma sp. , M.
anisopilae, and AMF biofertilizers on the growth of oil palm seedlings.


The experiment was conducted in a greenhouse using a 70x80 cm sized polybags filled
with 50 kg of Ciomas soil. Germinated oil palm was used as plant material and planted in polybag
and add with empty fruit bunches oil palm (EFBOP) as mulch. DT38 and DT41 isolates were
cultured in the media then transferred to PDA medium and inoculated into polybags. Mycorrhizal
inoculum is in the form of spores, hyphae and infected roots. Germinated oil palm was planted on
the polybag and the EFBOP was added as mulch. In the treatment of mycorrhizal fertilizer, the
dosage of inorganic fertilizer was 50% of the recommendation dose while others were 100% of
inorganic fertilizer. The experiment was arranged in completely randomized design to test nine
treatments i.e. 1) without fertilizer, 2) 100% dose of inorganic fertilizer, 3) EFBOP, 4) EFBOP+T.
pseudokoningii+DT38, 5) EFBOP+T. pseudokoningii+DT41, 6) EFBOP+T. pseudokoningii+DT38+
Metharizium anisopilae, 7) EFBOP+T. pseudokoningii+DT41+Metharizium anisopilae, 8) EFBOP+
T. pseudokoningii+DT38+Metharizium anisopilae+AM fungi, 9) EFBOP+T. pseudokoningii DT41+
M. anisopilae+AM fungi. Each treatment was repeated 3 times. Observations made on the growth of
oil palm.


Observations of plant height showed that fertilization increased height of plants while
EFBOP solely suppressed the height growth of plant (Table 1). The application of Trichoderma sp.
and M. anisopilae and arbuscullar mycorrhizal fungi (AMF) enhanced the height of palm seedling.

Table 1. The height and leaf number of oil palm seedlings (9 months) in each treatment tested

Treatment Height (cm) Leave number
Withou fertilizer
100% inorganic fertilizer
EFBOP
EFBOP+Trichoderma DT38+T pseudokoningii
EFBOP+ Trichoderma DT41+T pseudokoningii
EFBOP+ Trichoderma DT38+T pseudokoningii +Meth
EFBOP+ Trichoderma DT41+T p+Meth
EFBOP+ Trichoderma DT38+T p+Meth+AMF
EFBOP+ Trichoderma DT41+T p+Meth+AMF
106 ab
119 ab
81 a
130 b
130 b
129 b
133 b
126 b
123 ab
19 a
19 a
20 a
20 a
20 a
19 a
20 a
20 a
18 a
Note: Figure (s) in each column followed by the same letter is not different according to Duncan (P < 0.05).

th
However, the application of EFBOP as mulch in term of plant height was not significantly
different compared with those were not treated (without fertilizer) and 100% inorganic fertilizer.
These results indicated that the plant height variable is not affected by EFBOP and inorganic
fertilizer application. The absence of the influence of fertilization and the addition of EFBOP as
mulch plants may caused the soil already contains enough nutrients. Inoculation treatments DT 41
+ T. pseudokoningii or DT 38 + T. pseudokoningii without or in combination with M. anisopilae, and
EFBOP as mulch significantly resulted in higher plant height compared to the application of EFBOP.
These results indicated that the application of Trichoderma sp. DT 38, DT 41, M. anisopilae, T.
pseudokoningii in combination with EFBOP yield positive effect on plant height. Positive influence is
probably due to the decomposition process carried out by DT 38 and DT 41, while M. anisopilae
seems to have an effect on the prevention of Oryctes.as a plant pest. The same was observed in
the treatment of DT 38 + T. pseudokoningii + plus M. anisopilae and AM fungi. AM fungi can be
symbiotic with the roots of oil palm and the symbiosis can enhance nutrient uptakes, especially P
which contributes to increase plant height. In addition, the treatment was shown that application of
AMF (fertilizer 50%) showed a similar plant height with plants that 100% fertilized .These results
demonstrated that the application of AMF biofertilizer increased the efficiency of inorganic fertilizer
by 50%. The increasing inorganic fertilizer efficiency by using AMF symbiosis has also been
reported by other researchers. Some mechanisms that occur are by increasing the reach of roots,
and mineralization of organic P through the extraction phosphatase. The application of DT 41 + T.
pseudokoningii + M. anisopilae + and AMF biofertilizer was not significantly different with those of
DT 38 + T. pseudokoningii + M. anisopilae + and AM fungi in term of plant height.
Treatment of EFBOP increased the number of leaves compared to 100% inorganic
fertilizer and the unfertilizer treatment (Table 1). The application of EFBOP provides the same
number of leaves with the inoculation of DT41 or DT38 and the T pseudokoningii accompanied by
the application of M. anisopilae and AMF biofertilizer. However there is no significantly differences
between the number of leaves of all treatments tested in the blank, 100% inorganic fertilizer, or
mulching EFBOP. Interaction between AM fungi with DT 38 is better compared to the interaction of
those fungi with DT41 especially demonstrated by the number of leaves.
The fresh weight of leaves increased significantly with the addition of inorganic fertilizers
as well as giving EFBOP as mulch. Similar results were also observed in the treatment of EFBOP
addition which is accompanied by DT 38, DT 41, T. pseudokoningii, M. anisopilae and AMF
biofertilizer. It was shown that the efficiency of inorganic fertilizer can be achieved by the application
of AMF biofertilizer combined with either DT 41 or DT 38. Similar results are also shown on the
variables fresh weight of stem. Fresh weights of oil palm seedlings stem with inorganic fertilizer is
higher than thethe blank (Table 2). Nevertheless, the fresh weight of stem between 100% inorganic
fertilizer and application of EFBOP as mulch and blank werenot significantly different. The addition
of DT 41 and DT 38, which is accompanied by T. pseudokoningii and M. anisopilae results a fresh
weight of stem that were not significantly different compared to those with the addition of EFBOP as
mulch or 100% inorganic fertilizer. The application of EFBOP as mulch, AMF biofertilizer and 50%
inorganic fertilizer yield fresh weight of stem that is not significantly different to 100% inorganic
fertilizer treatment. These results indicated that the application of AMF biofertilizer improves
inorganic fertilizer efficiency as much as 50%.
Compared to the fresh weight of the stem appears that the effect of the treatments being
tested was more visible on the fresh weight of leaf variables. Application of EFBOP accompanied
by DT 41 and T. pseudokoningii addition produced the highest fresh weight of leaves. Similar
results were also observed in the treatment of EFBOP as mulch with DT 38, DT 41 or accompanied
by M. anisopilae. As for DT 38 leaf fresh weight significantly higher compared with the blank when
combined with M. anisopilae and AMF biofertilizer.

th
Table 2. The fresh weight of oil palm seedlings (9 months) in each treatment tested

Treatment
Fresh weight (g)
Leaf Stem Shoot Root Total

Without fertilizer
EFBOP
EFBOP+DT38+T p.
EFBOP+DT41+T p.
EFBOP+DT38+T p+Meth
EFBOP+DT41+T p+Meth
EFBOP+DT38+T p+Meth+AMF

450 a
850 b
863,33 b
733,33 ab
1066,67 b
833 b
883,33 b
900 b
716,67 ab

833,33 a
1433,33 ab
1583,33 ab
1683,33 ab
2000 b
1566,67 ab
1750 ab
1533,33 ab
1416,67 ab

1283,33 a
2250 ab
2466,67 ab
2416,67 ab
2733,33 b
2400 ab
2633,33 ab
3433,33 ab
2133,33 ab

783 a
1017 ab
967 ab
933 ab
1183 b
933 ab
1000 ab
783 a
1017 ab

2066 a
3267 b
3433 b
3349 b
3916 b
3333 b
3633 b
4216 b
3150 b

Fertilization treatments increased fresh weight of shoots as well as the addition of EFBOP
as mulch. The application of DT 41+T. pseudokoningii and DT 38+T. pseudokoningii either
accompanied by M. anisopilae or not resulted in fresh weight of shoots that are not significantly
different compared to those with 100% inorganic fertilizer and EFBOP as mulch. This result shows
that the effect of DT 41, DT 38 and M. anisopilae is not significantly different on the fresh weight of
shoots. However the application of DT 41+T. pseudokoningii and DT 38+T. pseudokoningii
accompanied by M. anisopilae and AMF biofertilizer yield shoots fresh weight equal to 100%
fertilization. These results indicated that AMF biofertilizer application increased the efficiency of
inorganic fertilizer, although this treatment may not significantly increased the fresh weight of shoots
of oil palm seedlings.
Root fresh weights were not significantly different in the treatment of 100% inorganic
fertilizer, EFBOP as mulch, and EFBOP+DT 38 + T. pseudokoningii and DT 41+T. pseudokoningii
accompanied by M. anisopilae or without M. anisopilae. The same result observed in the treatment
of DT 41 or DT 38+T. pseudokoningii+M. anisopilae accompanied wth AMF biofertilizer. Other study
demonstrated that the application of DT 41 and DT 38 or AMF biofertilizer increase the root fresh
weight. The same result was observed in the total oil palm seedlings fresh weight.

Table 3. Dry weight of oil palm seedlings (9 months) in each treatment tested

Dry weight (g)
Treatment Leaf Stem Shoot Root Total

Without fertilizer
EFBOP
EFBOP+DT38+T p.
EFBOP+DT41+T p.
EFBOP+DT38+T p+Meth
EFBOP+DT41+T p+Meth

123,33 a
220 a
205 a
201,67 a
225 a
196,67 a
188,33 a
168,33 a
126,67 a

231,67 a
361,67 a
453,33 a
386,67 a
463,33 a
460 a
438,33 a
410 a
425 a

355 a
582 ab
658 ab
588 ab
688 b
657 b
627 ab
578 ab
551 ab

138 a
215 ab
182 ab
278 b
212 ab
140 ab
165 ab
128 a
145 ab

493 a
797 b
840 b
866 b
900 b
797 b
792 b
726 b
698 b

The addition of 100% inorganic fertilizer increased dry weight of oil palm stems as well as
the treatment of EFBOP as mulch (Table 3). Similar result was observed in mulching treatments
EFBOP with by DT 41, DT 38 which with T. pseudokoningii and M. anisopilae and AMF biofertilizer.
Nevertheless, the results of statistical tests indicated that there is no significanly differences
between dry weight of plants fertilized with 100% treatment and other treatments. Similar results
th
were also found in variable weight of dry leaves, shoot, roots, and oil palm seedling. It seems that
the application of EFBOP as mulch can be combined with the inoculation of Trichoderma sp, M.
anisopilae and AMF biofertilizer. Hence the application of AMF biofertilizer reduced the doseage of
inorganic fertilizer as much as 50%. The effect of treatment to Ganoderma infection is likely could
be suppressed in this experiment.

References

Baon, J. B., 1998. Konversi lengas tanah melalui pemberian bahan organik dan mulsa. Warta Pusat Penelitian
Kopi Kakao. 14(1):61-68.
Broeckling C D, A K Broz, J Bergelson, D K Manter J M Vivanco. 2008. Root exudates regulate soil fungal
community composition and diversity. Appl. Environ. Microbial. 74(3), 738-764.
Komariah, S. Prihartini, T. dan Suryadi, M.E. 1993. Aktivitas Mikroorganisme dalam Reklamasi Tanah Gambut
In: Prosiding Pertemuan Teknis Penelitian Tanah dan Agroklimat : Bidang Kesuburan dan Produktivitas
Tanah. Puslit Tanah dan Agroklimat. Bogor. Hlm. 105-113.
Murugamandam S., D. W. Israel, W. P. Robarge. 2009. Activities of nitrogen-mineralization enzymes associated
with soil aggregate size fractions of three tillage systems. Soil Sci Soc Am J. 73, 751-759.
Nurani, D., Parmiyanti , S., Purwanta, H., Angkoso, G., Koesnandar. 2007. Increase pH of peatsoil by microbial
treatment. Internatoinal Symposium and Workshop on Tropical Peatland. Yogyakarta, 27-31 August.
Rousk, J., P C Brookes, E. Baath. 2009. Contrasting soil pH effects on fungal and bacterial growth suggest
functional redundancy in carbon mineralization. Appl. Environ. Microbiol. 75, 1589-1596.
Sparling, G.P. 1998. Soil microbial biomass, activity and nutrient cycling as indicator of soil health. In: Pankhurst,
C., Doube, B.M, Gupta, V.V.S.R. (eds). Biological Indicators of Soil Health, Wallingford: CABI
Publishing.
Vallad, G.E, L. Cooperband, and R.M Goodman. 2003. Plant foliar desease suppression mediated by
composted forms of paper mill residuals exhibits molecular features of induced resistance.
Physiological and Molecular Plant Pathology 63 (2003) 65-77.
White, P. M., C. W. Rice. 2009. Tillage effects on microbial and Carbon dynamics during plant residue
decomposition. Soil Sci Soc Am J. 73, 138-145.

th
The Use of RAPD Marker on Gambiers Breeding Program

Hamda Fauza
a*
, Jamsari
a
, Istino Ferita
a
, Ade Noverta
a
, Azmi Dhalimi
b
,
Ahmad Denian
c
, Murdaningsih H. Karmana
d

a
Faculty of Agriculture of Andalas University, Padang, Indonesia
b
Center for Agricultural Technology Assessment and Development, Bogor, Indonesia
c
Medicinal and Aromatic Crops Research Institute, Bogor, Indonesia
d
Faculty of Agriculture of Padjadjaran University, Bandung, Indonesia
*Corresponding author: Faculty of Agriculture Andalas University, Kampus Limau Manih 25163
Tel: +62 751 72776; Fax.: +62 751 72702; mobile : +62 8156119287 ;
[email protected]

Abstract

Low productivity is one of the problems faced by farmers in gambier (Uncaria gambir) plants cultivation. This
problem is mainly caused by the use of low yield gambir cultivars. Although breeding effort has been initiated
since several years ago, no significant result has been achieved until now. This is due to inadequacy of
molecular investigations in this species. Molecular aspects are commonly related with protocol for DNA
preparation and molecular markers which are important so that it will speed up the breeding program. The
objectives of the research were to optimize the DNA isolation procedures using different protocol and type of
materials, to optimize DNA amplification procedures, and (3) to find out RAPD primers indicating high level of
polymorphisms. The research was done from May to November 2009 in the Laboratory of Biotechnology and
Plant Breeding, Faculty of Agriculture, Andalas University. DNA isolation procedure and type of materials were
assessed. DNA isolation was performed using four different protocols. Type of materials tested consisted of
seven treatments. Optimizing PCR condition and RAPD primer selection delivered basic information of optimum
PCR condition. A number of 50 RAPD primers were randomly selected. The results recommended the
application of CTAB-based method protocol, using young meristem leaves for DNA isolation.

Keywords: gambier, breeding, RAPD

Introduction

Low productivity is a major problem in gambier (Uncaria gambir) plant development. Crop
productivity ranges between 400 and 600 kg per ha (Dinas Perkebunan Sumatera Barat, 1998;
Roswita, 1990). Meanwhile the potential of this plant can reach 2100 kg per ha of dry resin
(Sastrahidayat & Soemarsono, 1991). The low productivity is due to the use of low yield varieties.
Meanwhile, the use of improved varieties is one determining factor in increasing crop productivity. In
the cultivation of gambier, there is no information of using high yielding varieties.
Compared with other commodities, research and development of gambier plant breeding is
still far behind. With the use of biotechnology is expected the lag, especially in the field of plant
breeding can be pursued. Studies of molecular aspects of the basic information that will be useful
as an initial step in gambier plant breeding programs
During the previous decade, strategy for the evaluation of genetic variability was carried
out through the approach of anatomy, morphology, embryology, and physiology. This approach now
has been fasilitated with molecular techniques. The development of biotechnology in particular
science called molecular markers based on polymorphisms found in proteins or DNA, has been
widely facilitate research in disciplines such as taxonomy, ecology, genetics, and plant breeding
(Weising, et al, 1995).
In the field of plant breeding, using fingerprinting techniques have been applied to various
aspects and types of plants. Various examples can be mentioned, among others, is its application
to rice. Wu and Tanksley (1993) reported the identification of allele-specific microsatellite found in
th
indica and japonica rice types. The results are then followed by the use of PCR techniques to
identify microsatelite polymorphism possessed by the upland rice and other rice cultivars. Virk et al
(1995) using the RAPD technique for the distinction between the types of rice cultivation and to
identify possible duplication of cultivars. Besides the rice crop, the application of molecular markers
has also been applied to other fields. Meanwhile, for gambier plants, Fauza, et al. (2007) in early
research on diversity studies of gambier concluded that RAPD markers have a broad genetic
variability. But in this study there are several obstacles in the method of DNA isolation and RAPD-
PCR method technique is not stable yet, and limited use of polymorphic primers for gambier plants.
This study aimed to obtain the DNA isolation method for the gambier plant, to find
information on material characteristics for DNA isolation, to find a method (program) appropriate in
RAPD-PCR technique for gambier plant, and to obtain primers polymorphic in plants gambier
characterization techniques based on RAPD-PCR.


The research was done from May to November 2009 in the Laboratory of Biotechnology
and Plant Breeding, Faculty of Agriculture Andalas University. Two informations namely: DNA
isolation procedure and type of materials were assessed. Experiment of DNA isolation procedure
performed four protocols as treatments, i.e.: (1) Saghai-Maroof, et al. (1984), (2) Doyle and Doyle
(1990), (3) Krizman, et al. (2006), and (4) An Michiels et al. (2003). Experiment for type of materials
applied seven treatments, namely: (1) fresh young leaf, (2) fresh old lead, (3) fresh young leaf
stored at -20C for one week, (4) fresh young leaf stored at 4C, (5) young leaf stored at room
temperature (25C) for one week, (6) young leaf stored with silica gel for one week (7) etiolated
fresh young leaf. Optimizing PCR condition and RAPD primer selection; these experiments
delivered basic information of optimum PCR condition that could be used in variability and pedigree
analysis based on RAPD molecular technique. Optimization had been done by applying some
levels of annealing temperature i.e.: 35C; 37C; 40C; 42C and 45C. These annealing
temperatures will be combined with one or two cycle groups. Besides some level of DNA
concentration (5; 10; 15; 20; 25; 50; and 100 ng/reaction) and concentration of primer (5; 10; 20; 50;
and 100 pmol/reaction) applied. A number of 50 RAPD primers were randomly selected.


Optimization of DNA Isolation
Of the four isolation procedures attempted, it seems that the protocol based on Doyle and
Doyle (1990) produced the highest total DNA concentration. The ratio of the intensity of DNA
fragments isolated by Doyle and Doyle (1990) showed 2-5 times higher than the standard DNA
used. With the DNA isolation protocol based on Saghai-Maroof et al. (1984), there was no alleged
DNA pellets obtained. While isolation by using a protocol based on Krizman et.al (2006) and based
on An Michiels et. al, (2003) for the isolation of DNA-containing plant samples sap, the results
obtained was also not optimum .
The success of protocols based on Doyle and Doyle was likely caused by the presence of
phenol compounds was mixed with Chloroform-Isoamylalcohol in one stage of isolation. Phenol is
known as a compound that is effective enough to separate the protein from cell organelles. It is
known that plant cells are very rich in polyphenols. These substances are contaminants for the
DNA isolation from gambier plant tissue. However for other species, the use of phenol during DNA
isolation process is needed (Jamsari, 2003)
Of the several types and characteristics of materials used for DNA isolation was found that
young leaves of gambier plants in fresh condition and young leaves stored in silica gel, were good
th
materials for the isolation of gambier plant DNA. It is characterized by the discovery of DNA pellet
after the extraction process, which in turn is also evidenced by the results of electrophoresis
analysis. While other materials did not show DNA pellet after the precipitation process.
At this stage the attempt to isolate DNA from various plant tissues by several methods was
carried out. Isolation of DNA from fresh young leaves by the CTAB method (Doyle and Doyle, 1990)
and DNA with DNA Kit produced better quality. While the isolation of DNA from young leaves that
were stored with silica gel with CTAB method produced DNA with poorer quality than those from
fresh leaves, but by using a DNA kit produced DNA with a fairly good quality. In principle, the
resulting DNA can be used to the process of PCR-RAPD amplification. Optimization results of DNA
with CTAB method are shown in Figure 1.

M 1 2 3 4

M = Lambda 50. 1,2,3 = fresh young leaves, 4 = young leaves stored in silica gel

Figure 1. The examples of optimization results of gambier plant DNA isolation.

Optimization of RAPD-PCR technique
Optimization of RAPD amplification was done by modifying the temperature and time of
the stages of the amplification process of some methods and programs from various sources,
including: method of Williams, et al. (1990) and Ready to Go PCR Kit (RTG-PCR Kit). Based on the
results of the optimization program that will be applied in the amplification program was that
recommended by Williams, et al. (1990), as showed in Table 1.

Table 1. RAPD PCR amplification program of gambier plant

Process Temperature (C) Time Total cycles
Initiation of denaturation 96 2 min 1
Denaturationi 94 30 sec
45

Anneling 36 1 min
Extention 72 2 min
Final extention 72 5 min 1
Pause 4 ~

Primer Selection
To obtain a high degree of polymorphism, primers were selected by using random operon
dekamer primer technology (Almaeda, USA). As the DNA template used in the selection of this
primer DNA pool consisting of five DNA genotype gambier based phenotypic appearance is thought
to have a distance kinship. Selections of primer for subsequent experiments based on the number
of bands (fragments) and the sharpness of the resulting ribbons. Selection was carried out on 50
types of primer RAPD method and program optimization. The primer selection was conducted at
two-phase. In the first phase used 25 primers.Three of the 25 primers, were used were for the
analysis of individual selection, the OPN-06, OPE-18 and OPY-08. Each band primer produced
between 0-5 bands.

th
Table 2. List of RAPD primer and PCR product characteristics obtained

The second stage was the repeatation of the selection of 25 primers and the best three in
the first phase. DNA template used consisted of five different genotypes of first stage. Based on
the results of 28 RAPD primer amplification with DNA pool gambier, all tested primer products were
found in the DNA mixture. It means thar all the selected RAPD primers has the potential to be used
in the selection of individual gambier plant DNA. Products produced ranged from 4-14 fragments of
DNA. Fragments generated from the primer selection of this second stage were better than the first
stage. This is due to the different DNA pool used in this experiment. Therefore RAPD primer that
can be recommended for the analysis of kinship is the OPN-06, OPE-18 and OPY-08. More detail
can be seen in Table 2 and the results of amplification of DNA pools with 28 primers RAPD
gambier shown in Figure 2.

M 15 16 17 18 19 20 21 22 23 24 25 26 27 28

M 1 2 3 4 5 6 7 8 9 10 11 12 13 14

Description: sample mentioned in each of them according to the primary number in Table 2.

Figure 2. Amplification of gambier DNA pools with 28 primer RAPD.

No

Primer

Name

Se c uen ce s

N umber of
fragments

F ragmen t

Ch ara c teristi c s

1.

OPA - 11

CAA TCG CCG T

8

Fragment is quite clear, but it's rather difficult to be

s c oring

2.

OPA - 12

TCG GCG ATA G

4

Fragments are clear and easy to be

s c oring

3.

OPA - 15

TTC CGA ACC C

6

Fragments are clear and easy diskoring

4.

OPA - 19

CAA ACG TCG G

8


s c oring

5.

OPB - 01

GTT TCG CTC C

14


s c oring

6.

OPB - 06

TGC TCT GCC C

10


s c oring

7.

OPB - 09

TGG GGG ACT C

7


s c oring

8.

OPB - 11

GTA GAC CCG T

9


s c oring

9.

OPF - 08
GGG ATA TCG G

5


s c oring

10.

OPK - 06

CAC CTT TCC C

8


s c oring

11.

OPL - 13

ACC GCC TGC T

11


s c oring

12.

OPN - 19

GTC CGT ACT G

7


s c oring

13.

OPR - 11

GTA GCC GTC T

8

Fragmen ts are clear and easy to be

s c oring

14.

OPT - 16

GGT GAA CGC T

11


s c oring

15.

OPW - 11

CTG ATG CGT G

6


s c oring

16.

OPX - 01

CTG GGC ACG A

7


s c oring

17.

OPX - 04

CCG CTA CCG A

8


s c oring

18.

OPX - 07

GAG CGA GGC T

11

Fragment is quite clear, it's rather difficult to be

s c oring

19.

OPX - 09

GGT CTG GTT G

7

Fragments a re clear and easy to be

s c oring

20.

OPX - 15

CAG ACA AGC C

7


s c oring

21.

OPX - 19

TGG CAA GGC A

8


s c oring

22.

OPY - 04

GGC TGC AAT G

11


s c oring

23.

OPY - 20

AGC CGT GGA A

10


s c oring

24.

OPB - 17

AGG GAA CGA G

8


s c oring

25.

OPF - 05

CCG AAT TCC C

6


s c oring

26.

OPE - 18*

GGA CTG CAG A

12


s c oring

27.

OPN - 06*

GAG ACG CAC A

10


s c oring

28.

OPY - 08*

AGG CAG AGC A

13


s c oring

* The best primer on the first stage selection.

th
Conclusions

The isolation of DNA for gambier generated good quality and quantity of DNA using the
CTAB method by protocol of Doyle and Doyle (1990) using young leaf tissue. Meanwhile, a
program that should be applied for RAPD-PCR amplification was a program recommended by
Williams, et al. (1990). About 50 selected primers could be used in gambier DNA amplification, but
three primers showed a high number of bands and fragments namely: OPE-18, OPN-06 and OPY-
08.

References

An Michiels, W. Van den Ende, M. Tucker, L. Van Riet, and A. Van laere. 2003. Extraction of high quality
Genomic DNA from latex-containing plants. Analytical Biochemistry (315): 85-89.
Dinas Perkebunan Sumatera Barat. 1998. Statistik Perkebunan. Dinas Perkebunan Sumatera Barat. Padang.
Doyle, J.J. and J.L. Doyle. 1990. Isolation of plant DNA from fress tissue. Focus 12: 13-15.
Fauza, H., I. Ferita, Murdaningsih,H.K., N. Rostini, dan R. Setiamihardja. 2007. Variabilitas genetik tanaman
gambir berdasarkan marka RAPD. Zuriat 18 (1): 93-99.
Jamsari. 2003. Construction of High-Density Genetic and Physical Maps Around the Sex Gene M of Asparagus
officinalis L. Published Dissertation-Schriftenreihe des Institut fur Plantzenbau und zuchtung. Cristian
Alberchts Universitat zu Kiel (3) 1-171.
Krizman,M, J.Jakse, D.Baricevic, B.Javornik, and M.Prosek. 2006. Robust CTAB-activated charcoal protocol for
plant DNA extraction. Acta Agriculturae Slovenica. 87:427-433
Roswita, D. 1990. Prospek tanaman gambir di Sumatera Barat. Bul. BIP Padang (01): 8-10.
Saghai-Maroof, M.A., Soliman, K.M., Sharm, P.D., Kubde, and S.A. Mulay. 1984. Ribosomal DNS spacer-length
polymorphism in barley : Mendelian inheritance, chromosomal location and population dynamic. Proc.
Natl. Acad Sci USA (81) : 8014-8018.
Sastrapradja, S., S. Dinimihardja, R. Soejono, N.W. Soetjipto, M.S. Prana. 1980. Tanaman Industri. PN Balai
Pustaka. Jakarta. 132 hal.
Weising, K., H. Nybom, K. Wolf., and W. Meyer. 1995. DNA Fingerprinting in Plant and Fungi. CRC Press, Boca
Raton. Florida. 322 p.
Williams, J.G.K., Kubelick, A.R., Livak, K.J., Rafalski, J.A., Tingey, S.V. 1980. DNA polymorphisms amplified by
arbitrary primers are useful as genetic markers. Nucleic acids Res. 18:6531-6535.
Williams, J.K., A.R. Kubelik., K.J. Livak, J.A. Rafalski, and S.V. Tingey. 1990. DNA polymorphisms amplified by
arbitrari primers are useful as genetic markers. Nucleic Acid Research. 18(22): 65316535.

th
Shorea leprosula: the Most Commercial Trees to Improve
Production-Natural Forest Productivity

Wahyudi
1)
Indrawan A.
2)
Irdika Mansur
3)
Prijanto Pamoengkas
3)

1)
Department of Forestry, Palangka Raya University
[email protected]

2)
PhD, Faculty of Forestry Bogor Agricultural University
3)
Faculty of Forestry, Bogor Agricultural University

Abstract

Deforestation rate in Indonesia is 1,8 million ha per year. This is due to low productivity of natural forest which is
just 0,25 m
3
ha
-1
year
-1
(compared with teak plantation forest: 8-10 m
3
ha
-1
year
-1
). Decrease in natural
regeneration and forest plantation were caused by stand competition and limited of light in the forest floor.
Efforts to improve production-natural forest productivity was by applying the Selective Cutting and Strip Planting
(SCSP) system. This system made optimum open area (strip) which is suitable to maximize the growth of
Dipterocarp species, especially Shorea spp as the most commercial trees in the natural tropical forest. This
research aimed to analyze and created modeling of growth and yield of Shorea leprosula plantation in the SCSP
system. The research was conducted on research plots of SCS in logged over production natural forest of PT
Gunung Meranti forest concession, Central Kalimantan Province. Analysis of data used growth modeling for
even-aged forest. The result showed that mean annual increment of Shorea leprosula plantation at 2, 11 and 16
year olds were 1,06 cm year
-1
; 1,22 cm year
-1
and 1,31 cm year
-1
in diameters, respectively. Based on even-
aged forest modeling, the first cycles of Shorea leprosula plantations was 32 year in the 125,14 m
3
ha
-1
of logs
(40 cm up of diameters), therefore Shorea leprosula plantations in the SCSP system could improve the natural
forest productivity until 262,72 times. The SCSP system with Shorea leprosula plants is very applicable in the
logged over-production natural forest to improve forest productivity.

Keyword: Selective cutting and strip planting system, Shorea leprosula, growth and yield, productivity

Introduction

Indonesia is third in the world after Brazil and Zaire in wide of tropical forest regions and
has the highest biodiversity too (Whitmore, 1975; Mac Kinnon, et al., 2000). However, the condition
of natural forest resources in Indonesia tends to face degradation in the quality and quantity along
with environmental changes nationally and also globally (Ministry of Forestry, 2008). Deforestation
and degraded forest in Indonesia are caused by increasing of resident and wood requirement
(Singh, et al. 1995) illegal logging, shifting cultivation, illegal mining, illegal occupation of land, forest
fire (Indrawan, 2008) conversion of forest (Saharjo, 2008), and poor forest management (Wahjono
and Anwar, 2008).
As comparison, in the year 1990s, logs production in Indonesia were 28 million m
3
coming
from 59,6 million ha of production forest. But in the year 2007, logs production decreased to
become 9,1 million m
3
from 27,8 million ha of production forest only. Deforestation and degraded
forest will continue to happen if there isnt repair of production forest management system in
Indonesia. Some researches of silvicultural system in Indonesia have been conducted since 1993
and applying of Selective Cutting and Strips Planting (SCSP) silvicultural system with intensive
silvicultural technique has been done limited to 25 forest concessions since 2005, using species of
Dipterocarp specially Shorea spp. Shorea leprosula is one of Dipterocarp species recommended to
be developed in strips area in SCSP system. Afterwards, research on influencing of gap size and
slope to increase growth and yield of Shorea spp plantation in the SCSP system is very needed to
support this system.
th
Based on the forest function, forests in Indonesia are divided into three regions i.e.
conservation forest, protection forest and production forest. Production forest can be divided into
some forest regions, in the form of virgin forest, logged over forest, low potential forest, bushes-
scrub, grassland and critical land. Logged over forest and low potential forest can be managed by
Selected Cutting and Strips Planting silvicultural system using Shorea spp, especially Shorea
leprosula.
This Research aimed to compile growth and yield modeling of Shorea leprosula that is
developed in the strips area. Research was expected to be used by stakeholders, specially for user
of SCSP system.

Methods

Research was conducted in the Permanent Sample Plots of Selective Cutting and Strips
Planting in the District of Mandau Talawang, Central Kalimantan Province that was planted in 2008
(age of 2 years), 1999 (age of 11 years), and 1994 (age of 16 years). Data were collected in 2010.
Measured parameters were diameters and high of Shorea leprosula at the aged 2 years,
11 years, and 16 years. Growth and yield of Shorea leprosula pattern was formed according to to
the increment and time (years) functions through polynomial equation (Brown, 1997; Burkhart,
2003) that was:
y = c
1
+ c
2
x + c
3
x
2

Where: y : diameter (average)
x : time (years)
c
1
,c
2
,c
3 :
coefficient


The research results of Shorea leprosula plantation in the Permanent Sample Plots of
Selective Cutting and Strips Planting that is planted in 2008 (age of 2 years), 1999 (age of 11
years), and 1994 (age of 16 years) which were collected in 2010 were shown in Table 1.

Table 1. Mean annual increment of Shorea leprosula in the PSP of SCSP at 2, 11, and 16 years old

Age (year) Live (%)
MAI
Diameter (cm) High (m)
0 100 0 0
2 84.22 1.06 1.40
11 61.87 1.22 0.94
16 61.21 1.31 0.82

Table 1 showed that diameter mean annual increment (MAI) of Shorea leprosula since the
first time until 16 years old was always inreasing. MAI of Shorea leprosula was 1,36 cm/year at 16
years old with 61,21% of live. At the 16 years old, diameter and high of Shorea leprosula plants
were 21,22 cm and 13,1 m respectively. Growth and yield of Shorea leprosula was always
increasing until it achieved 30 to 40 cm in diameters (Wahyudi et.al. 2011).
Growth and yield of trees in the even-aged stand forest were different with those of
uneven-aged stand forests. Modeling must consider variation coefficient and deviation standard of
data. There were phenomena in the field that some plants in the monocultural plantation indicated
differences in growth level for each species. There are some species which grow very fast, fast,
slow and very slow. This phenomena is overcome by tending and thinning periodically.
th
Growth of plants can be assumed from time function. Diameter of plants will be getting
bigger progressively, but periodically growth must be mentioned in the model, so it needs the time
series of data to create modeling of growth and yield. Therefore, sigmoid curve to draw the growth
of yield of Shorea leprosula also needed the time series data. Modeling must accommodate all
information about species, environment, tending, increment and so on, which was made available
and trustworthy of growht and yield to create the justified modeling (Grant et al. 1997; Porte &
Bartelink 2001; Vanclay 2001). Modeling can simplify the complicated calculation composed of
several equations at the same time with some simulation expected.

A B C

Figure 1. Shorea leprosula plantation in the Selective Cutting and Strips Planting system at 2 years old (A), 11
years old (B) and 16 years old (C).

Modeling using polynomial equation based on increment of Shorea leprosula and time
functions (Brown 1997; Burkhart 2003) is as the following:

Y =0,0297x
2
+ 0,8208x + 0,3728 .................. R
2
= 86,89%

y : final diameter ; x : time (year) .

This model predicted that to achieve 50 cm up of diameter average, the time needed was 32 years
as shown in Figure 2. Correlation coefficient of this equations was 86,89%, accordingly, it indicated
that this equation can be used to predict growth and yield of Shorea leprosula plantation on the
Selective Cutting and Strips Planting system.

Figure 2. Growth and yield of Shorea leprosula plantation using modeling of polynomial equation.
Growth Equation of S. leprosula
y = 0,0297x
2
+ 0,8208x + 0,3728
R
2
= 0,8689
0
10
20
30
40
50
60
0 5 10 15 20 25 30 35
Time (year)
Diameter (cm)
th
Mean production of logs in PT Gunung Meranti (forest concession ) for 4 years (2007 to
2010) was 22,3 m
3
ha
-1
of logs. Whereas, based on even-aged forest modeling, the first cycles of
Shorea leprosula plantations for 32 years, the production was 125,14 m
3
ha
-1
of logs (40 cm up of
diameters), therefore Shorea leprosula plantations in the SCSP system could improve the natural
forest productivity until 262,72 times. The SCSP system of Shorea leprosula is very applicable in
the logged over-production natural forest to improve forest productivity. So, Shorea leprosula is
most commercial trees to improve Production Natural Forest productivity in the tropical forest.

Conclusion

Shorea leprosula plantation in the Selective Cutting and Strips Planting silvicultural system
can improve Production Natural Forest productivity in the tropical forest with applying the cutting
cycles as long as 32 years and predicted to produce 125,14 m
3
ha
-1
of logs.

References

Brown S. 1997. Estimating biomass change of tropical forest a primer. FAO Forestry Paper No.134. FAO USA.
Burkhart HE. 2003. Suggestion for choosing an appropriate level for modelling forest stand. In Amaro A, Reed
D, Soares P, editors. Modelling Forest System. CABI Publishing.
Coates KD, Philip JB. 1997. A gap-based approach for development of silvicultural system to address
ecosystem management objectives. Journal Forest Ecology and Management 99 (1997) 337-35.
Finkeldey R. 1989. An Introduction to Tropical Forest Genetic. Institute of Forest Genetics and Forest Tree
Breeding, Goettingen, Germany.
Fyllas NM, Politi PI, Galanidis A, Dimitrakopoulo PG, Arianoutsou M. 2010. Simulating regeneration and
vegetation dynamics in Mediterranean Coniferous Forest. Ecology Modelling Journal. 34.
Gadow KV, Hui G. 1999. Modelling Forest Development. Kluwer Academic Publishers.
Grant WE, Pedersen EK, Marin SL. 1997. Ecology and Natural Resource Management. Systems Analysis and
Simulation. John Wiley & Sons, Inc.
Kozlowski TT, Pallardy SG. 1997. Physiology of Woody Plants. Academic Press.
Porte A, Bartelink HH. 2001. Modelling mixed forest growth: a review of models for forest management. Eco.
Model. Journal.
Radonsa PJ, Koprivica MJ, Lavadinovic VS. 2003. Modelling current annual height increment of young Douglas-
fir stands at different site. In Amaro A, Reed D, Soares P, editors. Modelling Forest System. CABI
Publishing.
Rodriguez F, De La Rosa JA, Aunos A. 2003. Modelling the diameter at breast height growht of Populus
euramericana plantation timber in Spain. In Amaro A, Reed D, Soares P, editors. Modelling Forest
System. CABI Publishing.
Vanclay JK. 2001. Modelling Forest Growth and Yield. Applications to Mixed Tropical Forest. CABI Publishing.
Wahyudi. 2009. Selective cutting and line enrichment planting silvicultural system development on Indonesian
tropical rain forest. In: GAFORN-International Summer School, Geor-August Universitt Gttingen and
Universitt Dresden, Germany.
Wahyudi, Indrawan, Mansur, and Pamoengkas. 2011. Growth and Yield of Plantation and Residual Trees in the
Intensified Indonesian Selective Cutting and Strips Planting System. Case Study on Kapuas District,
Central Kalimantan Province. Post-Graduate Program Bogor Agricultural University, Bogor.

th
Patogenity Test of Two Isolates of Ganoderma on Sengon Seedlings

Elis N. Herliyana
a,*
, Irfan K. Putra
a
, Darmono Taniwiryono
b
, Hayati Minarsih
b

a
Department of Silviculture, Faculty of Forestry, Bogor Agricultural University, Bogor, Indonesia
b
Indonesian Biotechnology Research Institute for Estate Crops (IBRIEC), Bogor, Indonesia
* Corresponding author: Department of Silviculture, Faculty of Forestry, Bogor Agricultural University,
Kampus IPB Darmaga Bogor (16680), Indonesia
Fax 0251626806,
[email protected]; [email protected]

Abstract

Sengon tree (Paraserianthes falcataria (L.) Nielsen) currently becomes a major forest tree species widely planted
by smallholders in Indonesia. Sengon often used by farmers as component planted in agroforestry system as
well as shade trees planted in between other crops such as coffee and cacao. Ganoderma infection causebasal
stem rot disease which is becoming more prevalent and causing significant loss in sengon tree and other estate
crops. This research is based on the attack of Ganoderma tothe shade tree, sengon. Therefore, it is important to
do a specific research on the process of the inoculation of Ganoderma to prevent such attack. The aim of this
research is to understand the effect of the inoculation to the sengon seedlings. There are two majors in the
research i.e. non inoculation and inoculation treatments. Each treatment consisted of three observation blocks
that are considered equal and each block consisted of four plants (the sengon seedlings age were one and a
half months) as replicates. The non inoculation treatments were all combinations of root and foodbase
treatments. Foodbase treatment itself is divided into two i.e. the sengon wood piece with varying size (3, 4, and
5 cm diameters) and PDA (Potato Dextrose Agar) without inoculation of Ganoderma spp. from Ciamis
area/region (isolates of Ganoderma from lamtoro) and isolates of Ganoderma from sengon plants) derived from
the collection of Forest Pathology Laboratory and will be called SP1 and SP2. The result showed that the control
has a better average growth compared to the inoculation treatment. The f pathogenity test shows that
Ganoderma SP2 has more pathogenic than Ganoderma SP1. the heights of seedlings that were inoculated with
Ganoderma SP2 are l lower than the heights of seedlingss that were inoculated with Ganoderma SP1. Root
treatments application showed that both controls and treatments blocks have better growth from sengon
seedlings using root cutting treatment. The effect on the growth of sengon seedlings showed that inoculated
seedlings in the wood with 3 centimeters diameter as a foodbase inhibit both their height and leaves growth
compared to the seedlings with 4 centimeters or 5 centimeters diameter of wood of the same foodbase.

Keywords: foodbase, Ganoderma, sengon (P. falcataria), Basal stem rot.

Introduction

Sengon tree (Paraserianthes falcataria (L.) Nielsen) currently becomes a major forest tree
species widely planted by smallholders in Indonesia. In Java, there is a total area of 400.000 ha of
community forest dominated by sengon from which 895.000 m3 wood are produced annually. The
wood of this quick growing tree is processed further by paper industries to become pulp or sawed
by lumber industries as a raw material for soft wood board. Sengon often used by farmers as
component planted in agroforestry system as well as shade trees planted in between other crops
such as coffee, cacao and banana. Ganoderma infection is becoming more prevalent and causing
significant loss in sengon tree in Indonesia. Once the tree is infected by this cosmopolitan fungal
pathogen, sooner or later its base will become totally rotten leading to the tree dead. The disease
incidence ranges from 3% to 26%. One hundred percent disease incidence has been reported to
occur in the second generation of replanting.
This basal stem rot disease spread amongst trees primarily through roots contact. The
fungus has rigid fruiting bodies plate (conk), with or without stem, the top surface often looks shiny
waxy brown to dark brown in color, the bottom surface looks porous creamy white in color.
th
Theyoften found attached to the base of the rotten tissues near soil surface. Basidiospores
produced from pores at bottom surface plays in important roles in the disease spread from the
infected tree to the fresh cut of the stumps. The disease symptoms look similar with those caused
by heavy water stress displaying weak pale to yellowish in color of the tree canopy which is
unrecoverable and leading to leaf dryness. The disease is difficult to be controlled, because when
the symptom is observed, the infected tree is usually cannot be saved anymore by any control
means. Turner (1981) in Zakaria et al. (2004) reported that at least there are 15 species of
Ganoderma in various places in the world, which caused basal stem rot disease.
Ganoderma is a fungus causing basal stem rot disease that usually attacks the roots of the
host range. This fungus attacks is commonly found in various types Leguminoceae (Henessy and
Daly 2007), Palmae (Turner 1981 in Zakaria et al. 2005), Rubiaceae (Hindayana et al. 2002). The
authors also found Ganoderma that attack the ebony tree (Ebenaceae). This research is based on
the attack of Ganoderma to ashade tree, sengon. Therefore, it is important to do a specific research
on the process of the inoculation of Ganoderma to prevent such attack. The aim of this research is
to understand how the effect of the inoculation to the sengon seedlings to find the control technique.

Methodology

This research was conducted from October 2009 - March 2010. This research was held in
a greenhouse of Department of Silviculture and Forest Disease Laboratory of the Department of
Silviculture, Bogor Agricultural University.

Preparation of Equipment and Materials Research
The study was started by the preparation of sterile soil and foodbase that include a piece
of wood with diameter 3, 4 and 5cm and foodbase a PDA (Potato Dextrose Agar). The supply of
sterile soil was done by autoclaving of soil mixed media and charcoal husk compost with the ratio
of 2:1:1. Autoclaving was done by the time adjacent to weaning so that the soil conditions results in
steaming plastic bags are not contaminated. The PDA foodbase was prepared in two ways that are
not inoculated or inoculated.
PDAs which were not inoculated by Ganoderma, was prepared simply by making sterile
PDA medium which is then placed in polybags at weaning. The preparation of PDA inoculated
media by Ganoderma was done in conjunction with the preparation of pieces of wood that also
were infected with fungus. Isolates of Ganoderma have been cultured in a sterile culture into sterile
jars containing both types of foodbase. Maturity level of culture can be seen quite well from the
morphology of the fungus and spread on a PDA or timber in the jar. The uninoculated pieces,
supplies quite done with skinning sengon logs that had previously been cut with a length of 5cm and
various diameters i.e. 3, 4 and 5 cm. The pieces of wood were then boiled in a pan for a few hours
before sterilized in an autoclave.

Weaning and Maintenance
Weaning were performed in the afternoon to prevent the death of seedlings due to the
stress. Weaning also performed each treatment to be easy in the preparation plant. After that,
sengon seeds will be slightly softened, about one or two days prior to adapt from the stress.

Providing treatment
There are two majors in the research i.e. non inoculation and inoculation treatments. Each
treatment consisted of three observation blocks that are considered equal and each block consisted
of four plants (the sengon seeds age were one and a half months) as replicates. The non
inoculation treatments were all combinations of root and foodbase treatments.
Foodbase treatment itself is divided into two i.e. the sengon wood pieces with varying size (3, 4,
th
and 5 cm diameters) and PDA without inoculation of Ganoderma from Ciamis area/region (isolates
of Ganoderma from lamtoro) and isolates of Ganoderma from sengon plants) derived from the
collection of Forest Pathology Laboratory and will be called SP1 and SP2. The total of treatments
are 10. Inoculation treatments were a combination of various treatments of root and foodbase which
has inoculated with Ganoderma. Types of Ganoderma were also included in a combination. The
total number of inoculation is 15 treats. Types of Ganoderma were also included in a combination.
Total for this inoculation tratement is 30 treatments.

Observation of the Treatment and Data Collection
The observation of the treatment was carried out daily with the parameters of the number
of young leaves and seeds of high accretion sengon. Data were collected on a tall sheet and
analyzed using SPSS. At the end of the study, the root shoot ratio data was taken to see the most
balanced growth among the treatments.
Data was taken on the inoculated sengon with Ganoderma, Determination of the presence
or absence of fruiting body of Ganoderma was documented. The seeds which were harvested and
cleaned were then grouped by the type of treatment and then the roots were separated from the
shoots (stems). Part of the seed that is classified as part of the plant roots are located just below the
former location of the branch or branches from the first base.
After the separation of shoots and roots, the weight of each seedling roots and stems were
measured to determine the fresh weight of roots and shoots of seedlings. After the fresh weight
measurements, parts of seeds were wrapped in a paper and dried in the oven for 24 hours at 110
0

C. The second measurement was done for both roots and shoots of each seedling to calculate the
dry weight of roots and shoots.

Data Analysis
The experimental design was used complete randomized design based on the assumption
that the research conducted on a homogeneous condition. Homogeneity test is based on
experiments which only require element differentiation of treatment given. The calculation is
performed with use of SPSS, while Duncan's test was used for further testing.


In general, the result of control treatments measurement has a better growth compared to
the inoculation treatment. This result can be seen on the accretion parameter of heights and
number of leaves. It is possible to do the observation on the treatment of the inoculation with the
negative growth tendencies. The height measurement seed, according to the regulation of The
Minister of Forestry no.3 in 2004, is the height measurement from the base of the plant seed to the
top growing spot using centimeter unit. From that definition, if the growing point is dead, then the
growing spot underneath can replace it, so the height will be reduced.
The pathogenicity test shows that Ganoderma SP2 has more pathogenic than Ganoderma
SP1. This result can be seen on the heights of seeds that were inoculated with Ganoderma SP2 are
lesser than the heights of seeds that were inoculated with Ganoderma SP1.
The root treatment application shows that both controls and treatments blocks have a
better growth than sengon seedlings using root cutting treatment. This result corresponds with
Deselina works (1999), where root cutting will produce more vigor seeds and stronger roots. This
positive result of root cutting application in inoculation treatment, reveals that infection rate of
Ganoderma is lower than the healing process as the effect of the cutting.
The effect on the size of sengon seedlings showed that inoculated seedlings in the wood
with 3 centimeters diameter as a foodbase hampered both their height and leaves growth compared
to the seedlings with 4 centimeters or 5 centimeters diameter in the same foodbase. This result
th
indicates that wood pieces with 3 centimeters diameter as a foodbase, is more optimal in spreading
Ganoderma than the 4 or 5 centimeters.
Application of foodbase type differentiation in sengon seedlings showed that wet
foodbases such as PDA is easier than dry foodbases such as wood pieces, in transmitting
Ganoderma into plants roots. This can be seen from the calculation where the inoculated sengon
seedlings with the wet foodbase such as PDA, has a higher disruption than the dry one. These
results occurred in height parameter. Root sprout ratio measurement in this research shows an
effect of the Ganoderma infection on the plant. General calculation of root sprout ratio will generally
support the result using SPSS. Root cutting treatments on seedling growth sengon resulted in high
seedling leaves and seedling growth better than the group without cutting the roots of sengon
seedlings (Figure 1 and 2).

Figure 1 Comparison of the rate of increase in the child leaves the root treatment. Grey block shows the
uncutting roots and red block shows the cutting roots.

Figure 2 Comparison of the high rough at the rate of root treatment. Grey block shows the uncutting roots and
red block shows the cutting roots.

Conclusion

The control treatments shows better growth compared to the inoculation treatments.
Inoculation treatments at high pathogenicity on seedlings derived from Ganoderma sengon sp2.
These were shown by the magnitude inhibition. These obtained from the average growth of the
inoculated seedlings sengon with parameters of the number of leaves and seedlings height.
Observations showed that sengon seedling growth better by cutting the roots treatments, both in the
controls and inoculation treatments.

References

Deselina. 1999. Respon Semai Ampupu (Eucalypthus urophylla ST Blake) Terhadap Pemotongan Akar, Input
Fosfor dan Lama Tinggal di Persemaian (skripsi). Fakultas Pertanian Universitas Bengkulu. Bengkulu
Henessy, C. dan Daly A. 2007. Ganoderma Diseases. Northern Territory Government, Plant Pathology,
Diagnostic Services. Darwin.
Hidayat, Jajat. 2002. Informasi Singkat Benih. Direktorat Perbenihan Tanaman Hutan dan Indonesia Forest
Seed Project. T. H. R. Ir. H. Juanda, Dago Pakar, Bandung.
Hindayana, Dadan et al. 2002. Musuh Alami, Hama dan Penyakit Tanaman Kakao. Direktorat Perlindungan
Perkebunan, Direktorat Jenderal Bina Produksi Perkebunan Departemen Pertanian. Jakarta.
Irwanto. 2006. Penilaian Kesehatan Hutan Tegakan Jati (Tectona grandis) dan Eucalyptus (Eucalyptus pellita)
pada Kawasan Hutan WANAGAMA I. Sekolah Pasca Sarjana Universitas Gadjah Mada. Yogyakarta.
Uncutting root

Cutting root

Uncutting root

Cutting root

th
Photita, W., Lumyong, S., Lumyong.,P., Ho, W.H., McKenzie,E.H.C. and Hyde, K.D. (2001). Fungi on Musa
acuminata in Hong Kong. Fungal Diversity 6: 99-106.
Turner, P.D. 1981. Diseases and Disorders of the Oil Palm in Malaysia. Oxford University Press.
Zakaria, Latiffah; Harikrishna Kulaveraasingham, Tan Soon Guan, Faridah Abdullah dan Ho Yin Wan 2005.
Random Amplified Polymorphic DNA (RAPD) and Random Amplified Microsatellite (RAMS) of
Ganoderma from Infected Oil Palm and Coconut Stumps in Malaysia. Asia Pacific Journal of Molecular
Biology and Biotechnology Vol.13 (1):23-24.

th
th
A PCR-based Technique for Detection Cylindrocarpon destructans,
the Causal Agent of Grapevine Black Foot Disease

Raed A. Haleem
a,
*, Samir K. Abdullah
b
, Jaladet M. S. Jubrael
c

a
Plant Protection Department, Faculty of Agriculture and Forestry, University of Duhok, Iraq
b
Department of Biology, Faculty of Science, University of Zakho, Iraq
c
Scientific Research Center, University of Duhok, Iraq
* Corresponding author:

Plant Protection Department, Faculty of Agriculture and Forestry,
University of Duhok, Iraq. Tel.: +4947504015992
[email protected]

Abstract

The symptoms of Grapevine black foot disease caused by Cylindrocarpon destructans including reduction of the
plant vigour with small-sized trunks, reduction in root biomass, black discolouration and brown to dark streaks in
wood mainly at the base of the rootstock. According to morphological and cultural characteristics of
Cylindrocarpon, all isolates from infected roots of declined plants were identified as C. destructans. PCR
technique was performed for accurate identification of C. destructans isolates. Ten isolates of the fungi were
selected from different locations. Those isolates were subjected to species-specific PCR assay. Total genomic
DNA was isolated from pure cultures of the isolates. The average DNA yields ranged between 1.5-6.7 g/ml with
a purity 1.6-1.8. The specific primers for C. destructans were used to amplify the ITS region of nuclear ribosomal
DNA (rDNA) containing ITS1, ITS2 and the intervening 5.8 rRNA genes of Cylindrocaropon. TheITS sequence
could successfully and appropriately confirmed that all isolates were correctly identified as C. destructans. This
fungus obtained from this study was reported for the first time in Iraq.

Keywords: Black foot disease, Cylindrocarpon destructans, Grapevine, PCR

Introduction

Species of Cylindrocarpon Wollenw. are common soil inhabitants that often associated
with roots of herbaceous woody plants. Grasso and Magnano di San Lio (1975) described black
foot symptoms from nursery plants with black discoloration and gum inclusions in xylem vessels of
affected rootstocks. Scheck et al. (1998) also described black foot symptoms as dark-brown to
black streaking in the vascular tissue of young (25 year-old) grapevines.
There are two negative impacts of this disease on nursery seedling production. First, these
fungi cause seedling mortality in nurseries up to 50% (Anderson et al. 1962; Anonymous, 1993).
Second, infected seedlings have a lower survival rate after out planting to reforestation sites. An
important factor compounding this problem is that in some cases the symptoms are not visible on
infected seedlings but disease can develop after transplantation.
Detection of plant pathogens directly from infected tissues has been reported for several
agricultural plant pathogens (Levesque et al. 1994 & OGorman et al. 1994). In addition, PCR has
been used to detect soil pathogens directly from infested soil (Henson et al., 1993). This molecular
detection approache is ideally suited for the study of root rot organisms because of the difficulty in
isolating and identifying some of these fungi. Hamelin et al. (1996) designed species-specific
primers (Dest1 and Dest4) to detect C. destructans from conifer seedlings. Using these primers in
direct PCR assays on DNA extracted from C. destructans cultures isolated from grapevines in
Portugal, obtained a DNA fragment of 400 bp; The universal primer ITS4 and the fungus-specific
primer ITS1F were used in a first-stage fungus-specific amplification, followed by a second-stage
amplification with the primers Dest1 and Dest4 using the PCR product from stage one. This is a
simple and reliable method for detection of Cylindrocarpon spp. directly from infected grapevines
th
(Nascimento et al., 2001).The objective of this study was develop an efficient and reliable detection
method based on PCR for the identication and detection of C. destructans from infected seedlings.


Fungal isolation
Fungal isolation was done using two methods, i.e. isolation method from vine root and
moist chamber isolation method.

Isolation from vine roots
Small pieces of vine roots collected from five locations in Duhok governorate ( Bajelor,
Badi, College nursery, Malta nursery and Nizarke) were surface sterilized respectively by placing in
70% ethanol for 30 s, 1% NaOCl for 1 min and again in 70% ethanol for 30 s and then dried by filter
papers. Pieces of sterilized tissues were plated onto 2% potato dextrose agar (PDA) (Himedia
Laboratories Pvt. Ltd. - India) containing 0.25 mg/ml chloramphenicol. Hyphae growing out from the
tissue pieces were cut and subcultured onto fresh PDA plates, and incubated at 252 C (Van
Niekerk et al, 2004).

Moist chamber method
Cuttings were made from vine roots and placed in 90 mm petridishes containing sterilized
moist filter paper. Plates were incubated at room temperature until fungal growth observed.
Propagules (spores, mycelia) were transferred to Potato-dextrose-Agar (PDA) plates. Pure cultures
of each isolate were obtained by excising a hyphal tip from colony margins and plating it onto fresh
PDA.

Phenotypical characterization
All isolates were grown on PDA and MEA at 25C in darkness or under NUV + fluorescent
illumination with a 12-h photoperiod (Philips /36W) for 10 days until cultures sporulated. The
colonies were further incubated for 20 days to determine the presence or absence of
chlamydospores. The diameter of 20 chlamydospores per isolate was measured. Length and width
of 40 conidia (microconidia and one-, two-, and three-septate macroconidia) were measured.
Isolated fungi were identified based on the characters in culture and on natural substrates (Domsch
et al, 1980; Watanabe, 2002; Petit & Gubler, 2005).

DNA extraction and PCR amplification of ITS region
Ten isolates (DC1-DC10) were selected to confirm the identification by a specific primer of
the ITS region. Isolates were collected from five locations in Duhok governorate (Bajelor, Badi,
College nursery, Malta nursery and Nizarke).
Genomic DNA was extracted according to a method reported by Borges et al. (1990). The
specific primers of C. destructans ITS region (Dest1 5-TTGTTGCCTCGGCGGTGCCTG-3, Dest4
5-GGTTTAACGGCGTGGCCGCGCTGTT-3) were used to amplify the ITS region of nuclear
ribosomal DNA (rDNA), containing ITS1, ITS2 and the intervening 5.8 rRNA gene (Hamelin et al.,
1996). The PCR reactions were carried out in a total volume of 25 l, in thin-walled, 0.5 l
Eppendorf tubes.Master mix was prepared for 12 samples of each fungus (10 isolates plus 2
control) by mixing 30 l of 10XPCR, 30 l of dNTPs, 24 l forward primer, 24 l Reverse primer, 12
l MgCL2, 4.8 l of Taq polymerase enzyme and de-ionized distilled water was added to a final
volume of 252l. The solution mixed and spun for 10 second in a microcentrifuge. Then, the mixture
was distributed in PCR tubes. All these steps were done on ice. Amplification was carried out in an
automated thermal cycler (Delphy 1000, Oracle Biosystems, MJ Research Inc., Watertown, MA,
USA) according to the following program: An initial denaturation at 94C for 4 min, after which 30
th
cycles of denaturation (1 min at 94C), primer annealing (1 min at 58C) and primer extension (1.5
min at 72C) were performed (Alaniz et al., 2007). A final extension was performed at 72C for 10
min Amplification reactions were conducted at least twice, in two separate experiments. For each
isolate, 5 l of PCR products were mixed with 7l loading buffer and then analyzed by
electrophoresis in 2% (w:v) agarose gels with 1xTBE buffer visualized by UV fluorescence.


Phenotypical characterization of C. destructans
Cylindrocarpon destructans (Zinssm.) Scholten, Neth. JL. PL. Path. 70 (Suppl. 2) 9 (1964).
Fig. (1) A C. Telemorph: Neonectria radicicola (Gerlach & L. Nillsson) Mantiri and Samules
Canada J. Bot. 79: 339 (2001).
Colonies on MEA reached a diameter of 78 mm on PDA and 80 mm on MEA after 20 days
at 25C. Colony surface slimy to felty; aerial mycelium typically sparse to felty, white to buff or a
shade of brown. Colony reverse was orange to dark brown. Conidiogenous cells formed apically on
densely, irregularly branching clusters of cells borne laterally on otherwise undifferentiated
vegetative hyphae. Conidiophores 65 m tall. Macroconidia cylindrical, mainly 4-celled, 18 45 (-
47) 4 8 m. Microconidia, cylindrical, 1-celled, 8 11 (-12) 3 4 m. Chlamydospores
yellowish brown, ovate to ellipsoidal, a few in a chain, 8 10 (-15) m in diameter. Conidial
dimensions were in concordance with the previous identification (Petit & Gubler, 2005).

A) Twenty- day old colony on PDA-left, and MEA-right . B) Microconidia and macroconidia. Scale bar: 30 m, C) Mycelia and
Chlamydospores, Scale bar: 15 m.

Figure 1. Cylindrocarpon destructans.

Molecular detection of C. destructans

Genomic DNA isolation and purification
Suitable yields of genomic DNA were obtained from repeated experiments with an average
yield of 1.5-6.70 g/ml and a purity of about (1.6-1.8) determined by spectrophotometer ratio
A260/A280. The molecular weight of DNA samples was estimated using 1% agarose gel
electrophoresis containing DNA sample as control (Fig. 2). Ratios above 2.0 correspond to RNA
contamination, while ratios below 1.6 suggest protein contamination (Sinha et al., 2001).
A
B
C
A
B C
th

M: represents unrestricted DNA as a standard molecular weight marker. Lane1- 7: Whole Genomic DNA of some C.
destructans isolates isolated from different locations of Duhok Governorate.

Figure 2. Agarose gel electrophoresis 1% at 70 volt for 45 minutes.

Species specific primers
All isolates of C. destructans collected from different locations of Duhok Governorate were
amplified by two specific primers (Dest1, Dest4) which were designed by Hamelin et al, (1996). A
PCR fragment of about 400-bp was obtained for all of them. The agarose gel electrophoresis of
amplified products with this specific primer is shown in Figure (3). Other investigators have used the
same primers to amplify the ITS region of C. destructans (Hamelin et al., 1996; Alaniz et al., 2007).

Lanes 1 (DC1)-10(DC10), C. destructans isolates. Lane 11, negative control of sterile distilled water; lane M, 1Kb Plus DNA
Ladder.

Figure 3. Agarose gel of the PCR products using primer pairs Dest1 Dest4.

This is the first molecular detection work on C. destructans in Iraq. In this study, the
differences in the intensity of bands were not taken in consideration; despite they may reflect the
differences in copy number of the priming sites in the individual genome. The band intensity may
also be attributed to the difference of DNA concentration of individual isolates. This method did not
require going through all classical methods and only in a few hours the results could be obtained.
This approach is particularly well suited to soil organisms that are difficult to identify or isolate
because of the presence of other aggressive species.
M 1 2 3 4 5 6 7 8 9 10 11

bp

1500

1000
900
800
700
600
500
400
033

M 1 2 3 4 5 6 7 8 9 10 11

bp

1500

1000
900
800
700
600
500
400
033

th
References

Alaniz, S.; M. Leon; A. Viceni; J. Garci'a-Jimenez; P. Abad-Campos and J. Armengol. 2007. Characterization of
Cylindrocarpon species associated with black foot disease of grapevine in Spain. Plant Dis. 91:1187-
1193.
Anderson,N.,D.W.French,andD.P.Taylor.1962.Cylindrocladium root rot of conifers in Minnesota. For. Sci. 8:378
384.
Anonymous. 1993. Insectes et maladies des arbres-Quebec. Ministe`re des Ressources naturelles du Quebec-
Ressources naturelles Canada. In:- Richard C. H., MG. Pierre Berube, and B. Bourassa. 1996.
Identication of Root Rot Fungi in Nursery Seedlings by Nested Multiplex PCR. Applied and
Environmental Microbiology. 62 (11): 40264031.
Borges M. I.; M. O. Azevedo; R. Bonatelli; M. S. S. Felipe and S. Astolfi-Filho. (1990). A practical method for the
preparation of total DNA from filamentous fungi. Fungal Genetics Newsletter. Volume (37). ISSN for the
online version : 1941-4765.
Domsch, K. H.; W. Gams and T. H. Anderson. 1980. Compendium of soil fungi. vol. I. Academic press. UK
Grasso, S. and G. Magnano Di San Lio. 1975. Infections of Cylindrocarpon obtusisporum on grapevines in
Sicily. Vitis 14: 3639.
Hamelin, R. C.; P. Brub; M. Gignac and M. Bourassa .1996. Identification of root rot fungi in nursery seedlings
by nested multiplex PCR. Appl. Environ. Microbiol 62: 40264031.
Henson, J. M., T. Goins,W. Grey,D. E. Mathre,and M. L. Elliot. 1993.Use of polymerase chain reaction to detect
Gaeumannomyces graminis DNA in plants grown in articially and naturally infested soil. Phytopathology
83: 283287.
Levesque, C. A., T. C. Vrain, and S. H. De Boer. 1994. Development of a species-specic probe for Pythium
ultimum using amplied ribosomal DNA. Phytopathology 84:474478.
Mantiri, F. R.; G. J. Samuels; J. E. Rahe and B. M. Honda. 2001. Phylogenetic relationship in Neonectria
species having Cylindrocarpon anamorphs inferred from mitochondrial ribosomal DNA sequences. Can.
J. Bot. 79: 334340.
Nascimento, T.; C. Rego and H. Oliveira. 2001. Detection of Cylindrocarpon black-foot pathogens in grapevine
by nested PCR. Phytopathol. Mediterr. 40: 357361.
OGorman, D., B. Xue, T. Hsiang, and P. H. Goodwin .1994. Detection of Leptosphaeria korrea with the
polymerase chain reaction and primers from the ribosomal internal transcribed spacers. Can. J. Bot.
72:342346.
Petit, E. and W. D. Gubler. 2005. Characterization of Cylindrocarpon species, the cause of black foot disease of
grapevine in California. Plant Dis. 89:1051-1059.
Scheck, H. J.; S. J. Vasquez and W. D. Gubler. 1998. First report of black-foot disease, caused by
Cylindrocarpon obtusisporum, of grapevine in California. Plant Dis. 82: 448.
Sinha, R. P.; M. Dautz and D. P. Hder. 2001. A Simple and Efficient Method for the Quantitative Analysis of
Thymine Dimers in Cyanobacteria, Phytoplankton and Macroalgae. Acta Protozoologica 40:187 195.
Van Niekerk, J. M.; P. W. Crous; J. Z. Groenewald; P. H. Fourie and F. Halleen. 2004. DNA phylogeny,
morphology and pathogenicity of Botryosphaeria species on grapevines. Mycologia 96:781-798.
Watanabe, T. 2002. Pictorial atlas of soil and seed fungi: Morphologies of cultured fungi and key to species (2
nd

ed.) CRC Press. 486Pp.

th
th
Photosynthetic Light Reactions in C
4
Photosynthesis

Naoya Nakamura
a
, Yuri Nakajima Munekage
a
, Akiho Yokota
a*

a
Graduate School of Biological Sciences, Nara Institute of Science and Technology
* Corresponding author: Graduate School of Biological Sciences, Nara Institute of Science and
Technology, 8916-5 Takayama, Ikoma, Nara, 630-0192 Japan
Tel.: +81 0743 72 5568; fax: +81 0743 72 5569.
[email protected]

Abstract

The most productive wild plants and crops use C
4
photosynthesis (Brown, 1999). C
4
photosynthesis requires the
coordinated functions of two cell types in leaves, namely mesophyll (M) - and bundle-sheath (BS) - cells (Hatch,
1987). Atmospheric CO
2
is initially fixed by phosphoenolpyruvate carboxylase (PEPC) in M cells. The resulting
products, C
4
acids are transported into BS cells where CO
2
is released by decarboxylation of C
4
acids and
refixed by riburose-1, 5-bisphosphate carboxylase/oxygenase (RuBisCO) functioning in the Calvin cycle (C
3

cycle). Since this process increase CO
2
levels at the site of RuBisCO in the BS cells, the oxygenase reaction of
RuBisCO is largely reduced and RuBisCO can achieve maximal catalytic activity of CO
2
fixation. Therefore, C
4

plants have higher potential efficiencies in the use of light, water and nitrogen than C
3
plants (Long, 1999). C
4

plants have evolved from ancestral C
3
plants (Sage et al., 2011). In C
4
plants, not only the CO
2
metabolism but a
manner of light reactions which is a process to produce ATP and NADPH used for CO
2
metabolism has been
changed. However, mechanism of light reactions and its physiological roles on C
4
photosynthesis are not yet
fully understood. Here, we introduce latest findings and perspectives of physiological roles of light reactions in C
4

photosynthesis.

Keywords: C
4
photosynthesis, cyclic electron flow, Flaveria, Zea mays

The structure of mesophyll and bundle-sheath chloroplasts: the regulation of grana
formation

Light reactions take place on thlakoid membranes in chloroplasts. The thylakoid
membranes are arranged in stacked (grana) and unstacked (stroma lamellae) in C
3
plants.
Supercomplex of photosystem (PS) II and light-harvesting complex of photosystem II (LHC-II) are
localized in grana thykoids while most of PSI and ATP synthase are localized in stroma lamellae
(Albertsson, 2001). The grana stacks are more developed in low light intensity than in high light
intensity, the changes are assumed to optimize the photosynthetic efficiency in C
3
plants (Ballantine
and Forde, 1970). In NADP-malic enzyme (ME) type C
4
plants such as Zea mays, Sorghum bicolor
and Flaveria trinervia, grana thylakoids are observed in the M chloroplasts like chloroplasts of C
3

plants, but BS cells possess chloroplasts where grana thylakoids are largely decreased, as shown
in Fig. 1 (Laetsch et al., 1965, Laetsch and Price, 1969, Hofer et al., 1992). Interestingly, grana
formation was observed in BS chloroplasts of maize leaves at very low light intensity but was
completely abolished at normal light intensity (Brangeon, 1973). Decrease in grana stacks of BS
chloroplasts is likely induced by high light signal and those systems would have been recruited from
C
3
plants during C
4
evolution.
LHC-II is suggested to be involved in grana formation by binding thylakoid membranes in
C
3
plants (Allen and Forsberg, 2001, Standfuss et al., 2005). LHC-II is mainly present as trimer on
grana thylakoids. It is reported that in Flaveria trinervia the amounts of LHC-II polypeptides in BS
chloroplasts is only slightly reduced compared with that in M chloroplasts (Hofer et al., 1992) and a
significant amount of LHC-II polypeptides are also detected in fractionated stroma lamellae
(Munekage et al., 2010). Moreover, in maize, LHC-II trimer is identified in BS thylakoid membranes
th
using Blue-Native PAGE, although BS chloroplasts of Maize are almost grana-free (Romanowska et
al., 2008). These results suggest that amounts of LHC-II polypeptide and the presence of LHC-II
trimer are not sufficient for grana formation. Perhaps the additional mechanism is involved in the
formation of thylakoid membranes with reduced grana in BS chloroplasts.

F. bidentis (C
4
)
F. pringlei (C
3
)
Fig. 1. Light micrographs of leaf transverse section of Flaveria species.
Development of
BS cells and
their chloropalsts

F. bidentis (C
4
)
F. pringlei (C
3
)
Fig. 1. Light micrographs of leaf transverse section of Flaveria species.
Development of
BS cells and
their chloropalsts

Figure 1. Light micrographs of leaf transverse section of Flaveria species.

Regulation of linear electron flow and cyclic electron flow around PSI in C
4
photosynthesis

Linear electron flow operates to produce the both ATP and NADPH. In linear electron flow,
the electrons excised from water molecules at PSII are transferred to PSI through the cytchrome b
6
f
complex, and finally NADPH is produced. Protons are transported across the thylakoid membranes
from stroma side to lumen side during the process of electron transfer. This proton gradient is used
for ATP synthesis (Fig. 2). On the other hand, cyclic electron flow around PSI (CEF1) contributes to
only ATP production. In CEF1, electrons are returned from accepter side of PSI to plastoquinone
which mediate electron transport from PSII to cytchrome b
6
f complex (Shikanai, 2007). This electron
transport contributes to form proton gradient without NADPH production. Two CEF1 pathways have
been identified in C
3
plants.

H
+
H
+
ATP
NADPH
PSI
PSI
Cyt.
b
6
f
complex
ATP
synthase
PGR5,
PGRL1
PC
Fd
NDH
complex
lumen
stroma
Thylakoid
membrane
H
+
H
+
PQ
Fd
NADPH
Fig. 2. Schematic model of PS1 cyclic electron transport
FQR pathway
NDH pathway

Figure 2. Schematic model of PS1 cyclic electron transport.

The first pathway is called as ferredoxin-plastoquinone reductase (FQR) pathway involving
PROTON GRADIENT REGULATION 5 (PGR5) and PGRL1 (Munekage et al., 2002, Dalcorso et al.,
2008). The other pathway is NAD(P)H dehydrogenase (NDH) pathway involving a plastidial NDH
Development of BS cells
and their chloroplasts
F. pringlei (C
3
)
F. bidentis (C
4
)
th
complex composed of the eleven plastid-coded subunits (NDH-A to -K) and the over 15 nuclei-
encoded subunits (Peng et al., 2011). In C
3
plants, the FQR pathway contributes for maintaining the
production ratio of ATP/NADPH and for photoprotection, whereas the NDH pathway functions in
stress resistance in C
3
plants (Munekage et al., 2004, Wang et al., 2006, Munekage et al., 2008).
Localization of the NDH complex and PGR5 on stroma lamellae and distribution of PSII and PSI on
thylakoid membrane suggest that CEF1 takes place in stroma lamellae (Rumeau et al., 2005,
Munekage et al., 2010).
In C
4
plants, increased CEF1 activity and decreased linear electron transport is induced. In
NADP-ME type C
4
plants, BS chloroplasts of mature leaves show the inhibition of PSII activity (Woo
et al., 1970). The composition of PSII complex in BS chloroplasts is investigated by many
researchers using Zea mays, Sorghum bicolor and Flaveria trinervia. Several studies are suggested
that the subunits of PSII complex, especially those of oxygen evolving complex are largely reduced
in BS chloroplasts compared with M chloroplasts (Sheen et al., 1987, Oswald et al., 1990, Hofer et
al., 1992). BS chloroplasts produce only limited amounts of ATP and NADPH from liner electron
flow activity, because in this chloroplasts, PSII activity is significantly inhibited (Schuster et al.,
1985). Since NADPH is supplied by decarboxylation of C
4
acids by NADP-ME, only ATP is required
to be produced in BS chloroplasts of NADP-ME type. The ATPs are considered to be produced by
CEF1 activity. Significant activity of CEF1 compared with C
3
plants has been reported in Zea mays,
Sorghum bicolor (Herbert et al., 1990, Asada et al., 1993). The higher amounts of NDH complex
and PGR5 in BS cell than M cell also supports activation of CEF1 in BS cell of NADP-ME type C
4

plants (Kubicki et al., 1996, Munekage et al., 2010). On the other hand, ATP demands are
increased in M chloroplasts in NAD-ME type C
4
metabolism. In Salsola laricina and Halocharis
gossypina carrying NAD-ME type C
4
photosynthesis, lower grana index and higher ratio of PSI/PSII
in M chloroplasts than BS chloroplasts are reported (Voznesenskaya et al., 1999). Moreover,
subunits of NDH complex are enriched in M chloroplasts of NAD-ME type C
4
plants (Takabayashi et
al., 2005). Activated CEF1 likely contributes to the ATP production in C
4
photosynthesis. However,
for final conclusion, it is need to investigate phenotype of transgenic plants in which genes involved
in CEF1 are knocked down.

References

Albertsson PA. 2001. Aquantitative model of the domain structure of the photosynthetic membrane. TREND in
plant science 6: 349-354.
Allen JF and Forsberg J. 2001. Molecular recognition in thylakoid structure and function. TREND in plant
science 6: 317-326.
Asada K, Heber U and Schreiber U. 1993. Electron flow to the intersystem chain from stromal components and
cyclic electron flow in maize chloroplasts, as detected in intact leaves by monitoring redox change of
P700 and chlorophyll fluorescence. Plant Cell physiol. 34, 39-50.
Ballantine IEM, Forde BJ. 1970. The effect of light intensity and temperature on plant growth and chloroplast
ultrastructure in Soybean. Amer. J. Bot. 57: 1150-1159.
Brangeon J. 1973. Effect of irradiance on granal configurations of Zea mays bundle sheath chloroplasts.
Photosynthetica 7: 365-372.
Brown HA. 1999. Agronomic implications of C
4
photosynthesis. In C
4
plant biology. Academic Press, San Diego.
Pp 473-508.
Cui YL, Jia QS, Y QQ, Lin GN, Kong MM and Yang ZN. 2011. The GDC1 gene encodes a novel ankyrin
domain-containing protein that is essential for grana formation in Arabidopsis. Plant physiol 155: 130-
141.
Dalcorso G, Pesaresi P, Masiero S, Aseeva E, Schunemann D, Finazzi G, Jolit P, Barbato R and Leister D.
2008. A complex containing PGRL1 and PGR5 is involved in the switch between linear and cyclic
electron flow in Arabidopsis. Cell. 132: 273-285.
Eberhard S, Finazzi G and Wollman FA. 2008. The Dynamics of Photosynthesis. Annu. Rev. Genet. 42: 463-
515.
th
Hatch MD. 1987. C
4
photosynthesis: a unique blend of modified biochemistry, anatomy and ultrastructure.
Biochim. Biophys. Acta. 895: 81-106.
Hofer HU, Santore UJ and Westhoff P. 1992. Differential accumulation of the 10-, 16- and 23-kDa peripheral
components of the water-splitting complex of photosystem II in mesophyll and bundle-sheath
chloroplasts of the dicotyledonous C
4
plant Flaveria trinelvia (Spreng.) C. mohr. Planta 186: 304-312.
Kubichi A, Funk E, Westhoff P and Steinmiller K. 1996. Differential expression of plastome-encoded ndh genes
in mesophyll and bundle-sheath chloroplasts of the C
4
plant Sorghum bicolor indicated that the complex
1 homologous NAD(P)H-plastoquinone oxidoreductase is involved in cyclic electron transport. Planta
199: 276-281.
Laestsch WM, Stetler DA and Vlitos AJ. 1965. The ultrastructure of sugar cane chloroplasts. Z.Pflanzenphysiol.
54: 472-474.
Laetsch WM and Price I. 1970. Development of the dimorphic chloroplasts of sugar cane. Amer. J. Bot. 56: 77-
87.
Long SP. 1999. Ecology of C
4
photosynthesis. Environmental Response. In C
4
plant biology. Academic Press,
San Diego. Pp 215-249.
Munekage Y, Hojo M, Meurer J, Endo T, Tasaka M and Shikanai T. 2002. PGR5 is involved in cyclic electron
flow around photosystem I and is essential for photoprotection in Arabidopsis. Cell 110: 361-
371.
Munekage Y, Hashimoto M, Miyake C, Tomizawa K, Endo T, Tasaka M and Shikanai T. 2004. Cyclic electron
transport around photosystem I is essential for photosynthesis. Nature. 429: 579-582.
Munekage YN, Genty B and Peltier G. 2008. Effect of PGR5 impairment on photosynthesis and growth in
Arabidopsis thaliana. Plant Cell Physiol. 49: 1688-1698.
Munekage YN, Eymery F, Rumeau D, Cuine S, Oguri M, Nakamura N, Yokota A, Genty B and Peltier G. 2010.
Elevated expression of PGR5 and NDH-H in bundle sheath chloroplasts in C
4
Flaveria species. Plant
Cell Physiol. 51: 664-668.
Oswald A, Streubel M, Ljungberg U, Hermans J, Eskins K, Westhoff P. 1990. Differential biogenesis of
photosystem II in mesophyll and bundle sheath cells of NADP malic enzyme type C
4
plants. A
comparative protein and RNA analysis. Eur. J. Biochem.190: 185-194
Peng L, Yamamoto H, Shikanai T. 2011. Structure and biogenesis of the chloroplast NAD(P)H dehydrogenase
complex. Biochim. Biophys. Acta. 1807: 945-953.
Romanowska E, Kargul J, Powikrowska M, Finazzi G, Nield J, Drozak A and Pokorska B. 2008. Structural
organization of photosynthetic apparatus in agranal chloroplasts of Maize. J. Biol. Chem. 283: 26037-
26046
Rumeau D, Linka NB, Beyly A, Louwagie M, Garin J and Peltier G. 2005. New subunits NDH-M, -N, and O,
encoded by nuclear genes, are essential for plastid Ndh complex functioning in higher plants. Plant Cell
17: 219-232.
Standfuss J, Scheltinga AC, Lamborghini M and Kuhlbrandt W. 2005. Mechanisms of photoprotection and
nonphotochemical quenching in pea light-harvesting complex at 2.5 A resolution. Embo J. 24: 919-928.
Sage RF, Christin PA and Edwards EJ. 2011. The C
4
plant lineages of planet earth. J. Exp. Bot. 62: 3155-3169.
Schuster G, Ohad I, Martineau B and Taylor WC. 1985. Differentiation and development of bundle sheath and
mesophyll thylakoids in maize. Thylakoid polypeptide composition, phosphorylation, and organization of
photosystem II. J. Biol. Chem. 260: 11866-11873.
Sheen JY, Sayre RT, and Bogorad L. 1987. Differential expression of oxygen-evolving polypeptide genes in
maize leaf cell types. Plant Mol. Biol. 9: 217-226.
Shikanai T. 2007. Cyclic electron transport around photosystem I: genetic approaches. Annu. Rev. Plant Biol.
58: 199-217.
Takabayashi A, Kishine M, Asada K, Endo T and Sato F. 2005. Differential use of two cyclic electron flows
around PS1 for driving CO2-concentrating mechanism in C4 photosynthesis. Proc. Natl. Acad. Sci.
USA 102: 16898-16903.
Wang P, Duan W, Takabayashi A, Endo T, Shikanai T, Ye JY, Mi H. 2006. Chloroplastic NAD(P)H
dehydrogenase in tobacco leaves functions in alleviation of oxidative damage caused by temperature
stress. Plant Physiol. 141: 465-474.
Woo KC, Anderson JM, Boardman NK, Downton WJS, Osmond CB, Thorne SW. 1970. Deficient photosystem II
in agranal bundle sheath chloroplasts of C
4
plants. Proc. Natl. Acad. Sci. USA 67: 18-25.

th
Heavy Metals Concentration in Irrigation Water, Soils and Fruit Vegetables
in Coastal Area, Kota Bharu, Kelantan, Malaysia

Aweng, E. R.
a
, Karimah, M.
a
Suhaimi, O.
a

a
Faculty of Agro Industry and Natural Resources, Universiti Malaysia Kelantan, Malaysia.
* Corresponding author: Faculty of Agro Industry and Natural Resources, Universiti Malaysia Kelantan,
Malaysia.
Tel: +06097717247; fax: +06097717232.
[email protected]

Abstract

This study was conducted to evaluate the levels of selected heavy metals namely Aluminium, Boron, Cadmium,
Iron, Lead, Manganese and Zinc in irrigation water, soils and selected fruit vegetables (brinjal, chilli and ladys
fingers) which were cultivated in Kampung Badang, Pantai Cahaya Bulan in Kota Bharu, Kelantan, Malaysia.
The water used for irrigation in Kampung Badang, Pantai Cahaya Bulan had the highest concentration of Boron
(3.5 ppm) followed by Manganese (1.105 ppm), Iron (0.233 ppm), Lead (0.22 ppm), Zinc (0.217 ppm),
Aluminium (0.214 ppm) and Cadmium (0.0853 ppm). However, in general, the quality of the irrigation water
complied with the Class IV, Interim National Water Quality Standard for Malaysia, INWQS, 1985 (standard for
irrigation water) and Food and Agriculture Organization of the United Nations (FAO) Standard (1985) except
Cadmium. The irrigation water results were also compared with the Indian Standard (Awashthi, 2000), where in
general, all the measured parameters complied with the standards except Cadmium (0.01 ppm) and Plumbum
(0.10 ppm). Meanwhile, the concentration of Aluminium, Iron, Boron, Zinc, Manganese, Lead and Cadmium in
soils were ranged from 2.858 - 3.5ppm, 3.753 3.92 ppm, 3.753 3.92 ppm, 0.667 1.133 ppm, 0.253 0.653
ppm and 0.68 1.307 ppm, 0.072 0.181 ppm and 0.0283 0.0844 ppm respectively. The concentrations of
heavy metals in soils were also complied with the Indian Standard (Awashthi, 2000) and the European Union
(EU) Standards (2002). In addition, the concentration of Aluminium, Iron, Boron, Zinc, Manganese, Lead and
Cadmium in vegetables ranged from 0.071 0.22 ppm, 1.28 2.76 ppm, 2.367 2.467 ppm, 0.273 0.32 ppm,
0.064 0.098 ppm, 0.0127 0.138 ppm and 0.0482 0.053 ppm respectively. All heavy metals analyzed in the
vegetables also complied with the Indian Standard (Awashthi, 2000), World Health Organization (WHO)/FAO
(2007) and EU Standards (2006).

Keywords: fruit vegetables, heavy metal, soil, ferum, manganese

Introduction

Contamination of the environment with toxic heavy metals has become one of the major
causes of concern for human kind. Heavy metals in surface water bodies, ground water and soils
can be either from natural or anthropogenic sources. The two basic categories of pollution are
organic and inorganic (Duke &Williams, 2008). Inorganic pollution is basically from heavy metals.
Chemical substances such as heavy metals are one of the factors which contribute to
environmental pollution, and it was believed that it can disrupt living ecosystem (Kabata-Pendias &
Pendias, 2001). Currently, anthropogenic inputs of metals exceed natural inputs due to increased
urbanization and industrialization. Industrial wastes, atmospheric deposition from crowded cities
and other domestic wastes are among the major sources of heavy metals in the surface water,
ground water and soils (Varalakshmi and Ganeshamurthy, 2010). On the other hand, heavy metals
such as Cadmium, Copper, Plumbum, Nickel, Chromium, and Mercury may be present in soil from
the parent materials during soil formations (Plaster, 2003). Soil is a supporting layer for all
organisms in the world. The most important thing is soil acts as a medium for plant growth which
can recycle the nutrient and resources needed by plants. Soil will absorb heavy metals in the
polluted river as well as ground water and these will cause side effect for vegetable growth. As root
th
grows in the soil, it will absorb water and nutrients in solution (Plaster, 2003). Heavy metals that are
attached with soil water and soil particles will be absorbed by plant roots and accumulated in
vegetables (Alirzaveya et. al. 2006). Another patch way for heavy metals to get into vegetables is
via irrigation water which is contaminated by heavy metals.
This present study was aimed at finding out the levels of contamination of seven heavy
metals viz. Aluminium (Al), Boron (B), Cadmium (Cd), Iron (Fe), Lead (Pb), Manganese (Mn) and
Zinc (Zn) in irrigation water, soils and selected fruit vegetables in Kampung Badang, Pantai Cahaya
Bulan in Kota Bharu, Kelantan, Malaysia. A number of studies had been conducted by researchers
to identify the levels of heavy metals in vegetables from various sources. Anita et. al. (2010) stated
that, waste water irrigation led to the accumulation of heavy metals in soil and consequently into the
vegetables, while, Miclean et. al. (2000) found out that the metal accumulation in vegetables grown
in the vicinity of industrial sites represents a potential risk for public health. Works by Garcia et. al.
(1981) had shown that some common vegetables are capable of accumulating high levels of metals
from the soils.

Materials and methods

The study sites covered the agriculture area around Kampung Badang, Pantai Cahaya
Bulan, Kota Bharu, Kelantan, Malaysia (Figure 1). Kampung Badang, Pantai Cahaya Bulan, a
suburban area located in the coastal area in the north west of Kota Bharu.

Figure 1: Study Area.

Samples of the edible fruity vegetables were randomly collected from 5 x 5 m area of two
different fields. The fruit vegetables namely brinjal (Solanum melongena), chilli (Capsicum anmum)
and ladys fingers (Hibiscus esculentus) were collected at fruiting stage or at least at 60 days after
planting. Five fruits were collected for each type of vegetables. The collected samples were stored
in polyethylene bags, each sample bag for each vegetable before taking them to the laboratory for
the analysis. The soil that was used to grow the vegetables was randomly collected. Each location
comprised three samples; one sample was taken from each type of vegetable soils. In addition, in
each type of vegetable soils comprised three points, where these three point samples were mixed
as one sample with a total weight of about 50 grams. Therefore, a total of three soil samples were
collected for this study. A metal spade was used to collect the soil at 5 cm depth from the surface.
The samples were then placed in plastic bags, each sample for each bag before taking them to the
Kg Badang,PCB
th
laboratory for analysis. The source of irrigation water for this cropland was tap water from Kelantan
Water Berhad. Water samples used for irrigation were collected in a 500 ml washed polypropylene
bottle and 1 ml of concentrated acid nitric (HNO
3
) was added to the samples to avoid microbial
activity. For heavy metal extraction, 1g ground wet sample of plant or soil was digested in 3 ml
concentrated nitric acid (HNO
3
) and 1 ml of concentrated hydrochloric acid (HCl) (3+1, (v/v) ). The
mixtures were oven heated for 3 hours at 40
0
C. After that, the samples were removed from the
oven and let them cool for a few minutes. Then they were diluted with 150 ml de-ionized water. The
samples were then adjusted to pH 5 to 6 via acid base adjustment with hydrochloric acid and
sodium hydroxide. Then, the samples were analyzed using Spectrophotometer DR5000.
Meanwhile, irrigation water analysis followed USEPA Approve for wastewater analyses and
adapted from Standard Methods for the Examination of Water and Wastewater (2005) via
Spectrophotometer DR5000.

Results and discussion

The results obtained showed that in soil, the concentration of Aluminium ranged between
2.9 ppm and 3.5 ppm, where soil for growing chilli and brinjal recorded 3.5 ppm and soil for growing
ladys fingers recorded 2.9 ppm. The concentration of Boron was between 0.67 ppm and 1.13 ppm
and the highest recorded in soil for grow ladys fingers. Meanwhile, Cadmium concentration
recorded between 0.028 ppm and 0.084 and the highest rercorded in soil for growing chilli. In
addition, the concentration of Iron was between 3.75 ppm and 3.92 ppm where the highest
concentration recorded in soil for growing brinjal. The concentration of Plumbum was between
0.072 ppm and 0.181 ppm where the highest recorded in soil for growing chilli. Manganese and
Zinc were also measured for this study where the results showed that, the concentration of
Manganese recorded was between 0.68 ppm and 1.31 ppm and Zinc recorded between 0.25 ppm
and 0.65 ppm (Figure 2, 3 and 4). All Pb, Cd and Zn values complied with the Indian Standard
(Awashthi 2000) and European Union Standards, EU (2002). Generally, concentration of Iron was
the highest followed by Aluminium, Manganese, Boron, Zinc, Lead and Cadmium.
Among the heavy metals measured in three types of fruit vegetables, Boron concentration
was the highest (2.37 ppm 2.47 ppm), where the highest concentration was recorded in brinjal
and Iron was the second highest (1.28 ppm 2.76 ppm), and where the highest concentration was
recorded in chilli. Meanwhile, the concentration of Cadmium ranged between 0.048 ppm and 0.053
ppm, where the highest concentration was recorded in brinjal. The concentration of Lead ranged
between 0.013 ppm and 0.138 ppm with brinjal that recorded the highest concentration. In addition,
the concentration of Zinc was ranged between 0.27 ppm and 0.32 ppm with the highest
concentration recorded in brinjal (Figures 2, 3 and 4). All Pb, Cd and Zn values complied with the
Indian Standard (Awashthi 2000), WHO/FAO (2007) and Commission Regulation, EU (2006).
The concentrations of Aluminium, Boron, Cadmium, Iron, Lead, Manganese and Zinc in
irrigation water that was collected were 0.214 ppm, 3.5 ppm, 0.085 ppm, 0.233 ppm, 0.22 ppm,
1.105 ppm and 0.217 ppm respectively. Pb, and Zn values complied with the Indian Standard
(Awashthi 2000), FAO (1985), and Class IV, Interim National Water Quality Standard for Malaysia
(INWQS 1985) but not Cd. The concentration of Cd in irrigation water recorded 0.0853 ppm
exceeded the safe limits standard (0.01 ppm). The concentration of heavy metals in irrigation water
in sequence were B>Mn>Fe> Pb>Zn>Al>Cd.
th

The results showed that, the trend of heavy metal concentrations in vegetables was similar
(positive correlation) with the trend of heavy metals concentrations in irrigation water. On the other
hand, the trend of heavy metal concentrations in soil was also similar with the concentrations in
vegetables and irrigation water except for Aluminium (negative correlation). Meanwhile, high
concentrations of iron and manganese in soil was believed to be due to salt water intrusion (Figure
2,3 &4).

Conclusions

High concentrations of heavy metals in soil and irrigation water led to the accumulation of
heavy metals in vegetables. Heavy metal concentrations varied among the test vegetables, which
reflected the differences in their uptake capabilities and their further translocation to edible portion
of the plants. The trend revealed that, high concentrations of Cd, Pb and Zn in soil and water led to
high concentrations in vegetables, even though the concentrations in all vegetables were below the
national and international permissible limits. Irrigation water was a dominant factor to determine the
concentrations of heavy metals in vegetables compared to soil because irrigation water normally led
to the accumulation of heavy metals in soil and consequently into the vegetables. Based on the
Figure 2: Concentration of heavy metals in brinjal,
soil for brinjal and irrigation water.
Figure 3: Concentration of heavy metals in chilli, soil
for chilli and irrigation water.

Figure 4: Concentration of heavy metals in ladys fingers, soil for ladys fingers and irrigation water.

th
results, it showed that, Boron was found to be the highest in irrigation water as well as in vegetables
but not in soil. The lower concentrations of heavy metals in vegetables were believed to be due to
the good quality of irrigation water and absence of pollution in soil in the study area. It could be
suggested that fruit vegetables in Kampung Badang, Pantai Cahaya Bulan were safe for
consumption.

Acknowledgements

We would like to express our deepest appreciation to the Dean of the Faculty of Agro Industry and
Natural Resources of Universiti Malaysia Kelantan for his support and guidance. We are also grateful to the Vice
Chancellor of Universiti Malaysia Kelantan for his permission to publish this paper. The paper would not have
been possible without the help from these individuals.

References

Alirzayeva, E. G., Shirvani, T. S., Yazici, M. A., Alverdiyeva, S. M., Shulurov, E. S., Ozturk, L., Ali-Zade, V. M.
and Cakmak, I. 2006. Heavy metal accumulation in Artemisia and foliaceous lichen species from the
Azerbaijan flora. Forest snow and landscape research. 80(3): 339-348.
Anita, S., Rajesh, K. S., Madhoolika, A. and Fiona, M. M. 2010. Risk assessment of heavy metal toxicity through
contaminated vegetables from waste water irrigated area of Varanasi, India. Tropical Ecology. 51(2S):
375-387.
APHA (American Public Health Association). 2005. Standard Methods for the Examination of Water and Waste
Water. American Public Health Association, Washington, DC.
Awashthi, S.K. 2000. Prevention of Food Adulteration Act no 37 of 1954. Central and State Rules as Amended
for 1999, Ashoka Law House, New Delhi.
Committee on Food Hygiene. Houston, United States of America, ALINORM 07/30/13.
Duke, C.V.A. and Williams, C.D 2008. Soil Pollution. In: Chemistry for Environment and Earth Sciences. CRC
Press: Taylor and Francis Group.
European Union. 2002. Heavy Metals in Wastes, European Commission on Environment (http: //ec.e
uropa.eu/environment/waste/studies/pdf/heavy metals report.pdf ).
European Union. 2006. Commission regulation (EC) No. 1881/2006 of 19 December 2006 setting maximum
levels for certain contaminants in foodstuffs. Official Journal of European Union L364/5.
FAO. 1985. Water Quality for Agriculture. Paper No. 29 (Rev. 1) UNESCO, Publication, Rome.
Garcia, W.J., Blessin, C.W., Inglett, G.E. and Kwolek, W.F. 1981. Metal Accumulation and Crop Yield for a
Variety of Edible Crops Grown in Diverse Soil Media Amended with Sewage Sludge. Environmental
Science and Technology. 15 (7): 793-804.
Interim National Water Quality Standard for Malaysia 1985. Malaysia: Department of Environment Malaysia.
Malaysia Environmental Quality Report, 2003. Interim National Water Quality Standards for Malaysia.
Department of Environment Malaysia.
Plaster, E.J. 2003. Heavy Metals Contamination: Soil Sciences and Management. (4
th
ed.) Thomson Delmar
Learning.
Varalakshmi, L. R. and Ganeshamurthy, A. N., 2010. Heavy metals contamination of water bodies, soils and
vegetables in peri urban areas of Bangalore city of India. 19
th
. World Congress of Soil Science, Soil
Solutions for a Changing World. 1 6 August 2010. Brisbane, Australia.
WHO/FAO. 2007. Joint FAO/WHO Food Standard Programme Codex Alimentarius Commission 13th Session.
Report of the Thirty Eight Session of the Codex.

th
The Contribution of Agriculture in a Local Greenhouse Gas Turnover

Arief Sabdo Yuwono

Dept. of Civil and Environmental Engineering, Bogor Agricultural University (IPB)
PO Box 220 Bogor, Indonesia. Tel.: +62 251 8627 225
[email protected]

Abstract

The general objective of this study is to analyze the contribution of agricultural sector in a local scale
greenhouse gas turnover. It includes identification and quantification of the entire agricultural activities regarded
as greenhouse gas sources as well as those concerned as greenhouse gas sink. The study was carried out in
2010 and based on a series of five years data compiled from a municipality in West Java Province as a case.
The greenhouse gas sources were categorized into four sectors covering energy sector, solid waste, agricultural
and animal husbandry sectors whereas the greenhouse gas sink was identified merely in agricultural sector. The
amount of a single greenhouse gas emission was calculated by multiplication between a source unit and its
corresponding emission factor. The total quantity of greenhouse gas emission generated by the municipality was
summation of the whole sources from the entire sectors. The amount of the whole greenhouse gas sink was
summation of the total sequestered carbon. The study result based on five years compiled data indicated that
the average municipality greenhouse emission was in the order of 14.0 MT CO
2
-e per year whereas the net sink
was approximately 0.05 MT CO
2
-e per year. The contribution of agricultural sector was merely 0.08 % of the
total municipality greenhouse gas sources while its contribution on the greenhouse gas sequestration (as sink)
was 2.39% of the emitted greenhouse gases. It can be concluded that based on the quantitative analysis, the
local agricultural sector is a manner to sequester atmospheric carbon.

Keywords: agricultural sector, greenhouse gas, source, sink, turnover.

Introduction

Global warming, or more properly, global climate change (GCC), may be the most serious
environmental challenge ever faced by mankind (Mackie and Cooper, 2009). There are many
uncertainties surrounding the issue of global warming. However, several things about the
phenomenon are certain. It is known that CO
2
and other greenhouse gases, such as CH
4
, absorb
infrared radiation by which earth loses heat. The levels of these gases have increased markedly
since about 1850 as nations have become industrialized and as forest lands and grasslands have
been converted to agriculture (Manahan, 2000). Global warming phenomenon which is nowadays
concerned as a serious worldwide problem is essentially able to be mitigated locally based on the
local governmental development program. The local governments can formulate action plans based
on their local greenhouse gas (GHG) mass balance and database. A local GHG turnover is
therefore necessary to estimate contribution of each sector involved in emitting the GHG.
Greenhouse gases which deal with infrared-absorbing trace gases (other than water vapor) consist
of carbon dioxide (CO
2
), methane (CH
4
), nitrous oxide (N
2
O) and chlorofluorocarbons (CFCs). CFC
was excluded from this study case due to the lack of CFC distribution and consumption data. The
objectives of this study are to quantify the entire agricultural activities regarded as greenhouse gas
sources as well as those concerned as greenhouse gas sink and to analyze the contribution of
agricultural sector in a local scale greenhouse gas turnover.

th

The study was carried out in 2010 and based on a series of five (5) years data compiled
from a municipality in West Java Province, called City of X, as a case. The greenhouse gas sources
were categorized into four sectors covering energy sector, solid waste, agriculture and animal
husbandry sector whereas the greenhouse gas sink was identified merely in agricultural sector. The
amount of a single greenhouse gas emission was calculated by multiplication between a source unit
and its corresponding emission factor as indicated in Box 1. The total quantity of greenhouse gas
emission generated by the municipality was summation of the whole sources from the entire
sectors. The amount of the whole greenhouse gas sink was summation of the total sequestered
carbon.

Box 1. General equation and the related emission factor for agricultural sector data source
CO
2
, CH
4
and N
2
O emission from wetland or dryland paddy field:
Data source: Centre Agency for Statistics, City of X, 2005-2009
Emission factor: IPCC Guidelines for National Greenhouse Gas Inventories, 1996
GHG mass = wetland area x plantation day x emission factor

Carbon sequestration by city re-greening program and estate crops plantation:
Data source: Centre Agency for Statistics, City of X, 2005-2009 and BPLH, City of X, 2009
Emission factor: IPCC Guidelines for National GHG Inventories, 1996
Carbon sequestration = area x emission factor

Greenhouse Gas Source and Sink in Agricultural Sector
Agricultural activities regarded as greenhouse gas sources and sink in The City of X
covers wetland paddy cultivation, dryland paddy cultivation, estate crops, and city re-greening
program. The amount of the absorbed carbon was estimated simply from the area of the paddy
cultivation. The similar case occurs in the estate crops as well. Therefore, the total amount of the
absorbed carbon by those plant species was calculated directly based on the area of the cultivation.

Contribution of Agricultural Sector in the Local Greenhouse Gas Turnover
The identified agricultural activities occurred in The City of X mentioned above are
compiled altogether as agricultural sector. The cultivated area by each of these activities was
identified and recorded by Centre Agency of Statistics, City of X. It was then compiled for five (5)
years (2005-2009), in order to calculate the GHG emission quantity generated by agricultural
sector. Other sectors contributing greenhouse gases are energy sector, solid waste generation, and
animal husbandry. The contribution of energy sector on the total greenhouse gas production was
estimated by multiplying the amount of the energy source quantity by its corresponding emission
factor. It covers all fossil fuel consumption for the city electricity, transportation, and industry. The
amount of the generated solid waste is assumed in the order of 0.51 kg/capita/day (IPCC, 1966). By
using the total population data of the City of X, the total amount of methane emission can be
estimated. For the parameter nitrous oxide (N
2
O), the estimation method is almost the same as
those used in the CO
2
and CH
4
parameters, except for the emission factor. Global warming
potential (GWP) of CO
2
is one, N
2
O is 21 whereas for CH
4
is 310.


Estimation of the emitted CO
2
from the wetland paddy field and dryland paddy field is
presented in Figure 1. It shows that in general there is tendency where the amount of emitted CO
2

from the wetland paddy field is decreasing with the year. This is due to the ongoing encroachment
of the modern irrigated agricultural area that was converted to be industrial area and other land
th
uses. In 2009 even, the total area of the wetland paddy field was less than a half of the total area in
2005 meaning that the amount of the emitted greenhouse gas becomes less than a half as well.

(a) (b)
Figure 1. CO
2
emission from wetland (a) and dryland (b) paddy field.

The amount of the sequestered GHG from dryland paddy field however, was not
decreasing in the period of 2005-2009. It showed that the CO
2
sequestration from dryland paddy
field in 2009 was almost threefold of that in 2005. This was simply due to the growing area of
dryland paddy field in the City of X. The amount of methane emission from the wetland and dryland
paddy field is presented in Table 1. It revealed that according to the paddy field area, the quantity of
the emitted methane varies directly with the total paddy area. The more paddy field area, the higher
amount of the methane emission, and vice versa. The generation of the methane in the wetland
paddy area is initiated by anaerobic condition of the inundated paddy field as it was commonly
practiced in conventional paddy cultivation system in Indonesia. As a result, methanogenic bacteria
become more active to generate methane in such kind condition. The relative contribution of
agricultural sector on total methane emission of The City X is presented in Figure 2. Agriculture
contributes merely 0.01 % of the total methane emission where the largest portion was contributed
by domestic solid waste due to the characteristic of the City X as an urban area. Another main issue
of an urban area is the scarcity of agricultural land. Therefore, total methane emission generated by
agricultural land is consequently relatively small.

Table 1. CH
4
emission from wetland paddy field

Area type
Year Area (ha)
Plantation day
(day/year)
Emission factor
1

(kg/ha/day)
kg CH
4
2
ton CO
2
-e
Wetland 2005 1959 200 0.096 37,613 790
2006 1242 200 0.096 23,846 501
2007 1364 200 0.096 26,189 550
2008 1055 200 0.096 20,256 425
2009 758 200 0.096 14,544 305
Dryland 2005 40 100 0.063 252.0 5
2006 50 100 0.063 315.0 7
2007 65 100 0.063 409.5 9
2008 120 100 0.063 756.0 16
2009 100 100 0.063 630.0 13
Data source: Centre Agency of Statistics, City of X (2005-2009)
1
IPCC Guidelines for National Greenhouse Gas Inventories, 1996
2
kgCH
4
= area x plantation day x emission factor

It is estimated that approximately 5 to 20 percent methane produced and released into the
atmosphere is a by-product of the anaerobic decomposition of waste. A significant source of this
type of methane production is solid waste disposal in landfills, where methanogenic bacteria break
th
down organic matter in the waste under anaerobic conditions to produce methane (Anonymous,
2002). The landfilling of municipal solid waste is a significant source of atmospheric methane (CH
4
),
contributing to1020% of anthropogenic methane emissions (IPCC, 2001 in Einola et al., 2008).
This is in line with the findings of Papageorgiou et al. (2009) stated that disposal of waste in landlls
generates methane that has high global warming potential.
The third concerned parameter of GHG in agricultural sector is nitrous oxide (N
2
O) where
its theoretical emission quantity was determined by areas of the wetland and dryland paddy field
that were multiplied by their corresponding emission factors. Relative contribution of agriculture
sector on total nitrous oxide emission was very small, i.e. merely 0.1 percent. Agricultural sector
was not an important source of GHG from the viewpoint of the generated nitrous oxide (N
2
O).

Table 2. CH
4
emission per sector expressed in ton CO
2
equivalent (CO
2
-e)

Sector Average (ton CO
2
-e)
Fossil fuel consumption 2,9E+05
Domestic solid waste 8,2E+06
Agriculture 5,2E+02
Animal husbandry 6,6E+02
CH
4
Total emission 8,4E+06

Figure 2. Relative contribution of agricultural sector on total methane (CH
4
) emission.

Cumulative and yearly rate of carbon sequestration by means of city re-greening program
is presented in Figure 3. The lowest part of the graph occurred in 2008 as a consequence of the re-
greening program that achieved 10.0 hectares merely whereas the average area of the re-greening
program normally was 23.8 hectares per year. In contrast however, the best success of the city re-
greening program was reached in the last year (2009) where The City of X showed their
commitment to reduce the greenhouse gas emission as re-greening area covered 41.2 hectares in
a year.
Another way of carbon sequestration mode that was contributed by the city was through
estate crop plantation (Figure 3). The identified crops in The City of X were papaya, banana, durian,
manioc, mango, corn, sweet potato, and others. Total area of the estate crop plantation was in the
range of 3049-3849 hectares per year that is spread over the sub-city area. By opening more
plantation area, the amount of the captured atmospheric carbon dioxide would become higher.
According to de Nevers (1995), the only methods we now know to slow or stop the buildup of CO
2
in
the atmosphere are to reduce the use of fossil fuels (gas, oil, coal, peat, lignite) and to stop the
deforestation of the tropical rain forests.

th

(a) (b)
Figure 3. Carbon sequestration by city re-greening program (a) and estate crop (b).

An important illustration of the emission profile of The City of X is an outline of the GHG
emission and the related carbon sequestration quantity. Analysis on the compiled data revealed that
agricultural sector plays a minor role in emitting greenhouse gas (GHG) as indicated in Table 3.
Percentage of the CO
2
emission from agricultural sector was merely 0.17% whereas its contribution
on CH
4
and N
2
O emission were only 0.01% and 0.06%, respectively. On the other side, however,
agriculture contributes about 2.39% (Table 3) sequestration process of the emitted carbon dioxide
back to the earth through photosynthesis process. It indicated that agriculture plays a significant
role in the greenhouse gas turnover in the local scale.
The quantity of the emitted methane (CH
4
) and nitrous oxide (N
2
O) were significantly
higher than the amount of emitted carbon dioxide (CO
2
). Such condition should be noticed carefully
since the warming effect of CH
4
and N
2
O are much stronger than CO
2
. According to Jones (1992),
although increasing atmospheric CO
2
is often assumed to be the major contributor to warming, the
combined effect of a number of trace gases, principally methane, nitrous oxide and
chlorofluorocarbons (CFCs), though present at concentrations that are two to six orders of
magnitude lower than CO
2
, can rival the effect of CO
2
because, per molecule they absorb infrared
radiation much more strongly.

Table 3. Outline of the GHG emission of The City of X and the carbon sequestration

Emission/
sequestration
GHG Sector Average quantity (2005-2009) [ton CO
2
-e] %
Emission CO
2
Paddy field 3.3E+03 0.17

CO
2
Total emission 2.0E+06 99.83
CH
4
Agriculture 5.2E+02 0.01

CH
4
Total emission 8.4E+06 99.99
N
2
O Agriculture 2.2E+03 0.06

N
2
O Total emission 3.6E+06 99.94
Grand total emission (source) 14E+06 0.24
Average contribution of agric. sector 2.0E+3 0.08
Sequestration CO
2
Sequestration by:

- Estate crops
4.8E+04 2.38

- City re-greening program
1.6E+02 0.01
Grand total sequestration (sink) 4.8E+04 2.39

th

Figure 4. Relative emission of The City of X based on GHG component (2005-2009).

More severe condition occurred in The City of X where GHG parameters of CH
4
and N
2
O
were absolutely much higher than CO
2
(Figure 4). As a consequence, the warming effect on the
atmosphere would be much higher too. The main potential reason for such condition was that the
people of The City of X generated solid wastes higher than the other Indonesian urban population.

References

Anonymous, 2002. Assessment of Greenhouse Gas Emissions from Solid Waste Disposal as a Result of the
Proposed New Zealand Waste Strategy. Ministry for the Environment. Reference Number 19518. New
Zealand.
de Nevers, N. 1995. Air Pollution Control Engineering. McGraw-Hill, Co. New York. Pp 506.
Einola, J.-KM., Sormunen, KM., Rintala, JA. 2008. Methane oxidation in a boreal climate in an experimental
landfill cover composed from mechanicallybiologically treated waste. Sci.of the Total Environ. 407:67-
83.
Jones, HG. 1992. Plants and Microclimate. A Quantitative Approach to Environmental Plant Physiology. 2
nd
ed.
Cambridge University Press, Cambridge, UK. Pp 428.
Mackie, KR and Cooper, CD. 2009. Landfill gas emission prediction using Voronoi diagrams and importance
sampling. Environ. Modeling and Software 24: 1223-1232.
Manahan, SE. 2000. Environmental Chemistry 7
th
ed. Lewis Publishers, Boca Raton, USA. Pp 898.
Papageorgiou, A., Barton, JR., and Karagiannidis, A. 2009. Assessment of the greenhouse effect impact of
technologies used for energy recovery from municipal waste: A case for England. J. of Environ.
Management 90: 2999-3012.

th
The Influence of Global Climate Indices on Rainfall Distribution Pattern and
Its Impact on Crop Yield in Gunung Kidul, Yogyakarta, Indonesia

Bayu DA Nugroho
a,*
, Hiromitsu Kanno
b
, Ryoji Sameshima
b
, Hiroshi Fujii
c
,
Larry CM Lopez
c

a
The United Graduate School of Agricultural Sciences, Iwate University, Japan
b
National Agricultural Research Center for Tohoku Region, NARO, Japan
c
Faculty of Agriculture, Yamagata University, Japan
* Corresponding author: The United Graduate School of Agricultural Sciences, Ueda 3-18-34,
Morioka, Iwate, Japan 020-8550. Tel.: +81 19 643 3408; fax: +81 19 641 9296.
[email protected]

Abstract

The correlation between the global climate index (SOI/SST), rainfall distribution and crop yield in rain-fed
highland areas was investigated. For this analysis, rainfall data were collected during the rainy season (October-
March) for the period 1981 to 2009 in Gunung Kidul district of Yogyakarta Province, which is one of the
important rain-fed crop producers in Indonesia. The rainfall distribution pattern found indicates that most of the
rainfall occurs in coastal areas, especially in the southern hilly areas, where the occurrence of the Southern
Oscillation Index (SOI) and Surface Sea Temperatures (SST) Nio.West are also highly correlated with rainfall.
Soybean yield is highly correlated with rainfall while dry land paddies, peanuts and wetland paddies yields show
a good correlation with SOI during January-February-March-April (JFMA).

Keywords: crop yield, rainfall, rain-fed area, SOI/SST

Introduction

Research on rainfall variability in Indonesia related to rain-fed agricultural areas is a critical
issue due to its relationship with El Nio and La Nia events. The delay of rainfall has a negative
effect on agricultural production in Indonesia. El Nio occurrences delayed rice harvesting in
Indonesia and creates instability in food security (Harger, 1995). In 1997, rice farming in the sub-
districts (Kecamatan) of Java decreased dramatically by 58% in wetland areas and 52% in dry land
areas (Irawan, 2002). The abnormal weather caused by El Nio events seriously disturbed crop
cultivation and the production of food and other commodities in the affected areas, mainly those
located in the rain-fed dependent highland areas.
Rain-fed highland areas are more affected by rainfall variability because of the topography
characteristics (Haylock and McBride, 2001). Rainfall variability in Indonesia correlates well with
global climate index, such as the Southern Oscillation Index (SOI) and the Sea Surface
Temperature (SST) pattern (Saji et al., 1999). At the same time, crop production in Indonesia is
influenced by rainfall variability and highland topography. Therefore, it is necessary to estimate
rainfall variability as influenced by the global climate indices (SOI and SST) in rain-fed highland
areas and its correlation with crop yields.
The aims of this study are to analyze the relationship between rainfall, global climate
indices SOI/SST and agricultural crops production based on the rainfall variability during the rainy
season from 1981-2009 in rain-fed highland areas.


Study Area
Gunung Kidul district is one of the rain-fed highland areas of Java Island, located between
746-709 S latitude and 11021-11050 E longitude. Based on elevation, Gunung Kidul district as
th
reported by the Agricultural Service for Food Crops and Horticulture (ASFCH) is divided into three
areas of which the northern border ranges between 200-700 meters above the sea level (m); the
center area is the lowland area with an elevation of 150-200 m, and the south area with a hilly
topography ranges from 0 to 300 m. A total of 92% of the agricultural land area in Gunung Kidul
district depends on rainfall, especially on October precipitation, as reported by the ASFCH (2006)
and the remaining 8% is irrigated. The mean annual rainfall in Gunung Kidul district is 2041
mm/year based on the record data from 1989-1998.

Secondary Data
Crops yield from 1990 to 2009 and rainfall data from 1981 to 2009 at twelve locations were
collected from the rainfall observation stations of ASFCH (2009). The SOI and SST data were
collected from the Japan Meteorology Agency (JMA) website
(http://www.data.jma.go.jp/gmd/cpd/db/elnino/index/dattab.html) and were averaged in Nio3 (5N-
5S and 150W-90W), Nio.West (15N-EQ and 130E-150E) and IOBW (20N-20S and 40E-
100E) areas, respectively. Spatial data of Gunung Kidul district with a scale of 1:25000 were taken
from the National Coordinating Agency for Survey and Mapping (Bakosurtanal) of Indonesia (2007).
Rainfall data were the average of cumulative rainfall during the rainy season (from October
to March) from 1981 to 2009 at each station. Steps in the data analyses were as follows: first,
mapping of rainfall during the rainy season (6 months, Oct-Mar and then separately Oct-Dec (OND)
and Jan-Mar (JFM) from 1981-2009. Second, in order to analyze the distribution of rainfall in
Gunung Kidul district, a regression analysis was conducted between rainfall during the rainy
season, 6 months and 3 months (OND and JFM) from 1981 to 2009 and the averages of SOI/SST,
to identify the global climate indicators that influence rainfall. Third, correlation analysis was
conducted between the average of rainfall during the rainy season and crop yields, and finally,
correlation analysis between the average of global climate indicators and crop yield during the rainy
season was conducted.
Correlation analysis between rainfall in the rainy season and crop yield, global climate
SOI/SST and crop yield was calculated only for the period 1990-2009 because of the data
availability on crop yield for this period.


Distribution of rainfall during the rainy season for the period 1981 to 2009
The analysis of rainfall distribution from 1981 to 2009 was carried out based on a six
months (Oct-Mar) and three months (OND and JFM) analysis. The distribution analysis shows that
in the southern coastal areas and in the inland western areas rainfall ranged from 1800-2200 mm,
while in the lowland central and northern areas rainfall was around 1500-1600 mm (Fig. 1). The
southern area is a mountainous area with a maximum elevation of 700 m. It caused moisture from
the Indian Ocean carried by the wind and moving horizontally produces dense clouds along the
mountain ranges. These clouds cause rain in the upper region known as orographic precipitation
(Roe, 2005), which is the reason why the windward side of the mountain range receives much more
precipitation than the leeward side.

th
1700
1
8
0
0
1
6
0
0
1
9
0
0
2
0
0
0
2
1
0
0
1
5
0
0
2
2
0
0
1
8
0
0
1900
1600
1
9
0
0
2
0
0
0
1
8
0
0
1
6
0
0
1
5
0
0
1
5
0
0
10 0 10 5 Kilometers
.

Figure 1. Distribution rainfall map during rainy season in Gunung Kidul district 1981 2009.

Relationship between the averages of rainfall and SOI/SST during 1981-2009
In Correlation analysis between the averages of rainfall during the rainy season and the
averages of SOI and SST Nio.West in all sub districts, only three sub district, which has significant
correlation, Panggang (r = 0.58), Playen (r = 0.44) and Rongkop (r = 0.49) sub-districts in p<0.01
and p<0.05. Panggang and Rongkop are the southernmost sub districts in the Gunung Kidul district,
which directly border with the Indian Ocean, whereas Playen sub district, located in the middle of
Gunung Kidul district, is poorly influenced by the Indian Ocean. Therefore, the area along the coast
shows a stronger correlation with SOI - SST Nio.West than the center area. The average rainfall
for the 9 other sub districts do not have significant correlations with the averages of SOI - SST
Nio.West, which are probably influenced by the mountainous terrain indirectly affecting the
correlation of rainfall and SOI.

Relationship between average rainfall and crop yield
Correlation analyses between average rainfall and crop yield during JFMA (January-
February-March-April) can be seen at Table 1.

Table 1. Correlations between the average of rainfall in rainy season and crops yield in JFMA

Dry land paddy Maize Soybean Peanut Wetland paddy
-0.15 -0.31 0.60** -0.04 -0.21
Pearson correlation coefficient
** Significant with p < 0.01

Based on Table 1, a strong correlation between average rainfall and crop yield during
JFMA is only for soybean yield. Therefore, from PS 2 farmers tend to grow soybean as the main
crop rather than dry land paddy in rain-fed highland areas. In the case of cassava yield, statistical
analysis cannot be done during JFMA from 1990 until 2009, because it is not harvested during
these months. Cassava is an annual plant, which is well adapted to drought and is harvested
between July and August.

Relationship between the averages of SOI and crop yield
The relationships between the averages of SOI/SST and crop yield indicated that SOI is
correlated with crop yield (dry land paddy, r = 0.50; peanut, r = 0.55 and wetland paddy, r = 0.55),
whereas no correlation between SST Nio.West and crop yield was found (Table 2). Based on
Table 2, average SOI during JFMA corresponds well with dry land paddy, peanut and wetland
th
paddy yields, and changes in the value of SOI influencing dry land paddy, peanuts and wetland
paddy yields.

Table 2. Correlation between average SOI and crops yield in JFMA

Dry land paddy Maize Soybean Peanut Wetland paddy
0.50* 0.28 0.25 0.55* 0.55*
Pearson correlation coefficient
* Significant with p < 0.05

The usefulness of global climate index and rainfall pattern to determine suitability of crops
is needed to help farmers in their decision taking, especially in rain-fed highland areas. Our results
indicate that averages of SOI and SST Nio.West are correlated with rainfall, especially in the
seaside southern hills areas.
In general, increases in the average SOI/SST Nio.West will influence the amount of
rainfall, and directly influence the cropping pattern. Our study found that increasing rainfall during
the rainy season (JFMA) from 1990 to 2009 increased soybean yield. Different results show that
averages of SOI corresponded well with dry land paddy, peanut and wetland paddy yield during
JFMA. Increases of SOI averages in JFMA by +1 will cause the increase of dry land paddy yield
during JFMA periods. The same trend can be observed for peanut and wetland paddy yield, in
JFMA.
Overall, our results show that most of the crops yield trend during the rainy season does
not correspond to global climate indices and rainfall. The main reason may be local cropping
patterns that still dominate regardless of the rainfall pattern and global climate index. Further
analysis of other rain-fed highland areas, which are different in elevation and in micro-scale (village)
by including crop yield data, is necessary.

References

Agricultural Service for Food Crops and Horticulture (ASFCH), GunungKidul district. 2006. Profil Tanaman
Pangan Kabupaten GunungKidul (In Indonesian). Pp 5 34.
Agricultural Service for Food Crops and Horticulture (ASFCH), GunungKidul district. 2009. Rainfall database in
Gunung Kidul district. Pp 10-130.
Harger, J.R.E. 1995. Air-temperature variations and ENSO effects in Indonesia, the Phillipines and El Savador:
ENSO Patterns and Changes from 1866-1993. Atmos. Environ 29: 1919-1942.
Haylock, M. and McBride J. 2001. Spatial coherence and predictability of Indonesian wet season rainfall. J.
Climate 14: 3882-3887.
Irawan, B. 2002 Stabilization of upland agriculture under El Nino-Induced climatic risk: Impact Assessment and
Mitigation Measure in Indonesia, Economics and Social Commission for Asia and the Pacific, CGPRT
Center WORKING PAPER No. 62.
Japan Meteorological Agency, 2010 El Nino Index data, retrieved from the statistical climate service at
http://www.data.jma.go.jp/gmd/cpd/db/elnino/index/dattab.html
National Coordinating Agency for Survey and Mapping (Bakosurtanal) Republic of Indonesia. 2007 Spatial data
for Gunung Kidul district at scale 1: 25000.
Roe,G.H. 2005. Orographic Precipitation. Annu. Rev. Earth Planet. Sci 33: 645-71.
Saji,N.H., Goswami, B.N.,Vinayachandran, P.N. & Yamagata,T. 1999. A dipole mode in the tropical Indian
Ocean. Nature 401: 360-363.

th
th
An Input-Output Analysis of the Economic Impact for Sustainable Rural
Development in Wonogiri District, Indonesia

Shintaro Kobayashi, Shigeki Yokoyama*, Satoshi Uchida, Yoshiko Iizumi

Japan International Research Center for Agricultural Scineces, Tsukuba, Japan
*Corresponding author: Social Science Division, Japan International Research Center for Agricultural Scineces,
1-1 Ohwashi, Tsukuba, 305-8686, Japan.
Tel.: +81 29 838 6343; fax: +81 29 838 6342.
[email protected]

Abstract

Wonogiri district located in Central Java is the water source of Solo River. There is a large multi-purpose
reservoir in the region. However, the reservoir is reported to be losing its function due to rapid sedimentation
caused by forest conversion and intensive farming. For sustainable resource management, assessment of
development strategies incorporating alternative agro-forest systems is required. This study, as a preparation for
the assessment of development strategies, was aimed to grasp regional industrial structure, using the input-
output analysis. The results showed that the importance of agriculture in the region was both as an income
source especially for unskilled labor and as financial base for purchasing manufactured goods. Therefore,
environmentally sound agro-forest systems need to be proposed so that strict environmental restriction on
agriculture can be avoided.

Keywords: sustainable rural development, input-output analysis, Wonogiri.

Introduction

Wonogiri district is located in Central Java, Indonesia and is the water source of Solo River
(Figure 1). There is a large multi-purpose reservoir in the region, and it has contributed to both flood
control and water utilization. However, the reservoir is reported to be losing its functions as a public
reservoir due to extremely rapid sedimentation. It is said that main reasons for the rapid
sedimentation is forest conversion and intensive farming induced by regional population increase
(JICA, 2007). In order to achieve sustainable resource management in the region, assessment of
development strategies incorporating alternative agro-forest systems is required. This study, as a
preparation for the assessment of development strategies, was aimed to grasp the regional
industrial structure and income multiplier effects by sector, using the input-output analysis, an
economic analysis method.

Figure 1. Location of Wonogiri District.
th

The input-output analysis was proposed by W. Leontief (e.g. Leontief, 1986) and it was
used for projections of impacts of changes in production technology, social environment, consumer
preference, or economic policy on an economy. Based on economic statistics or economic survey,
simulation models called input-output model were formulated. Simplified flow of the analysis was
as follows. Firstly, an input-output table which described all transactions among economic sectors
was estimated (Figure 2). Secondly, production technologies and traits of transactions were
abstracted from the table as the form of parameters called "input coefficients" (Figure 3). Lastly,
using the input coefficients, transactions between demand sectors and production sectors and
among production sectors were formulated to produce simultaneous equation for simulation (Figure
4). Based on the statistics of Wonogiri district, we estimated an input-output table. Tables 1, 2, and
3 show sector classification of the estimated table.

agriculture mining manufacturing services Consumer Government Investor Export
agriculture nnnnn 200 nnnnn nnnnn 3000 nnnnn nnnnn nnnnn nnnnn
mining nnnnn 50 nnnnn nnnnn 0 nnnnn nnnnn nnnnn 960
manufacturing nnnnn 100 nnnnn nnnnn 1000 nnnnn nnnnn nnnnn nnnnn
services nnnnn 10 nnnnn nnnnn 2000 nnnnn nnnnn nnnnn nnnnn
wage nnnnn 400 nnnnn nnnnn
profit nnnnn 200 nnnnn nnnnn nnnnn : Monetary value of annual transaction
Total Input nnnnn 960 nnnnn nnnnn : How much "mining" bought
: People's income from "mining"
: How much people consumed
Household
Demanders
Total
Output
Intermediate demand by producers Final demand
Suppliers
(Producers)

Figure 2. A sample structure of an input-output table. The table is estimated based on economic statistics or
economic survey of a target region. Row vectors in the table show the amounts of supply valued at
market prices. Column vectors show the purchase of goods and services.

agriculture mining manufacturing services
agriculture nnn/NNN 200/960 nnn/NNN nnn/NNN
mining nnn/NNN 50/960 nnn/NNN nnn/NNN
manufacturing nnn/NNN 100/960 nnn/NNN nnn/NNN
services nnn/NNN 10/960 nnn/NNN nnn/NNN
Demander (Producers)
Suppliers
(Producers)
input coefficient matrix A

Figure 3. Abstraction of information on production technology as the form of parameters called "input coefficient" A.

agriculture mining manufacturing services Consumer Government Investor Export
agriculture nnnnn 200 nnnnn nnnnn 3000 nnnnn nnnnn nnnnn nnnnn
mining nnnnn 50 nnnnn nnnnn 0 nnnnn nnnnn nnnnn 960
manufacturing nnnnn 100 nnnnn nnnnn 1000 nnnnn nnnnn nnnnn nnnnn
services nnnnn 10 nnnnn nnnnn 2000 nnnnn nnnnn nnnnn nnnnn
wage nnnnn 400 nnnnn nnnnn
profit nnnnn 200 nnnnn nnnnn nnnnn : Monetary value of annual transaction
Total Input nnnnn 960 nnnnn nnnnn : How much "mining" bought
: People's income from "mining"
: How much people consumed
Household
Demanders
Total
Output
Intermediate demand by producers Final demand
Suppliers
(Producers)
X Y X A = +

Figure 4. Formulation of technology A, production X, and demand Y in an economy.

th
Table 1. Production sectors

P1 Farm crops
P2 Livestock and products
P3 Forestry
P4 Fishery
P5 Mining and quarrying
P6 Oil and gas manufacture
P7 Other manufacture
P8 Electricity supply
P9 Gas supply
P10 Water supply
P11 Construction
P12 Trade, hotel, and restaurant
P13 Road transport
P14 Other transport
P15 Communication
P16 Financial services
P17 Real estate and business services
P18 Public administration and social services
P19 Personal and household services

Table 2. Demand sectors

D1 Private consumption
D2 Private investment
D3 Governmental consumption
D4 Public investment

Table 3. Value added sectors to supply primary factors to production

V1 Land
V2 Unskilled labor
V3 Skilled labor
V4 Capital
V5 Natural capital
V6 Indirect tax

In this paper, we drew skyline chart and derive income multipliers of economic activites.
Skyline chart revealed trade characteristics of target economy. Drawing method was as follows. An
input-output table could be expressed as follows:
M E F X A X + + = Eq. 1

where X is a column vector of total output, A is input coefficient matrix, F is a column vector of
domestic final demand, E is an export column vector, and M is an import column vector. Solving
Eq. 1, X can be decomposed into 3 inducing factors as follows:

M A I E A I F A I X + =
1 1 1
) ( ) ( ) (
Eq. 2

where the first term of right-hand side indicates the production induced by domestic final demand F,
the second term indicated the production induced by export E, and the last term indicated the
potential domestic production to be substituted for import M. Based on Eq. 2, a skyline chart shows
each factors relative contributions to production on the vertical scale, with 100% was representing
F A I
1
) (
. In addition, the horizontal scale showed the sectoral share in total production.

th
Income multipliers could be obtained by the following procedures. Assuming that import
was in proportion to domestic demand, Eq. 1 could be transformed as follows:

) (
~
F X A M E F X A X + + + =
Eq. 3

where M
~
is a diagonal matrix of import coefficients. Solving Eq. 3 for X, we obtain the following
equation.

{ } { } E F M I A M I I X + =

)
~
( )
~
(
1
Eq. 4

where
{ }
1
)
~
(

A M I I
is called Leontief inverse matrix and includes information on the industrial
structure of an economy. Supposing that
V
~
is a diagonal matrix of value added ratio to production
cost, income multiplier was column sums of a matrix
{ }
1
)
~
(
~
A M I I V
.


Based on an input-output table of Wonogiri district estimated for year 2005, we analyze
current situation of Wonogiri district. Major findings were as follows:
(i) Farm crop sector was the largest income source and accounts for 46% of regional gross
domestic products (Figure 5). This implied that environmental restriction on agricultural
activities would affect the standard of living in the region. Therefore, environmentally sound
agricultural systems including agro-forestry need to be proposed so that strict environmental
restriction can be avoided.
Farm crops
Trade, hotel,
restaurant
Road
transport
Public
administration
46%
13%
10%
11%

Figure 5. Share of income sources.

(ii) The district exported substantial amount of Farm crops and imports manufactured products
(Figure 6). This means that the district participates in a regional division of labor and an
interregional trade system. High self-sufficiency of Road transport seems to reflect the active
transportation of products including Farm crops.
(iii) Agricultural sectors had tendency to strongly induce income of unskilled labor. Trade, hotel,
and restaurant sector had also high value in income multiplier for unskilled labor (Table 4).
These facts implied that integrated activities consisting of agriculture and services such as
ecotourism was promising for pro-poor development.
This multiplier showed how much income of unskilled labor was induced by one unit of final demand
for each sector.

th
F
a
r
m
c
r
o
p
s
L
i v
e
s
t
o
c
k
a
n
d
p
r o
d
u
c
t s
F
o
r
e
s
t
r
y
F
i s
h
e
r
y
M
i n
i n
g
a
n
d
q
u
a
r
r
y
i n
g
O
i l a
n
d
g
a
s
m
a
n
u
f a
c
t
u
r
e
O
t
h
e
r
m
a
n
u
f a
c
t
u
r e
E
l e
c
t
r
i c
i t
y
s
u
p
p
l y
G
a
s
s
u
p
p
l y
W
a
t
e
r
s
u
p
p
l y
C
o
n
s
t
r
u
c
t
i o
n
T
r
a
d
e
, h
o
t
e
l , a
n
d

R
o
a
d
t
r
a
n
s
p
o
r
t
O
t
h
e
r
t
r
a
n
s
p
o
r
t
C
o
m
m
u
n
i c
a
t i o
n
F
i n
a
n
c
i a
l s
e
r
v
i c
e
s
B
u
s
i n
e
s
s
s
e
r
v
i c
e
s
P
u
b
l i c
a
d
m
i n
i s
t
r
a
t i o
n
P
e
r
s
o
n
a
l s
e
r
v
i c
e
s
Self-Sufficiency Import
100%
150%
200%
250%
300%
350%
400%
450%
500%
550%
600%
50%
0%
20% 40% 60% 80%
Farm crops
Road
transport
Trade, hotel,
restaurant
Public
admin.
Manufacture

Figure 6. Skyline chart. Horizontal axis shows share of production and vertical axis shows self-sufficiency rate.

Table 4. Income multiplier for unskilled labor

Trade, hotel, and restaurant 0.389
Farm crops 0.388
Forestry 0.324
Personal and household services 0.321
Livestock and products 0.310
Public administration and social services 0.285
Road transport 0.270
Fishery 0.227
Construction 0.218
Other manufacture 0.174
Financial services 0.155
Communication 0.152
Mining and quarrying 0.148
Water supply 0.137
Electricity supply 0.077
Real estate and business services 0.054

Conclusions

Income source share and the skyline chart showed the importance of agriculture both as
an income source and financial base for purchasing manufactured goods. Therefore, environmental
policies to restrict agricultural activities would affect the standard of living. In order to avoid reducing
income level in the region, environmentally sound agro-forest systems need to be proposed.
Income multiplier implied that Trade, hotel, and restaurant, as well as agricultural sectors, had a
strong power to induce income of unskilled labor. Therefore, integrated activities consisting of
agriculture and services such as ecotourism were promising for pro-poor development. The
remaining issues were crop-wise input-output analysis for decomposing Farm crop sector,
backward and forward linkage among sectors, and simulation analysis on income generation effects
of proposed community business models.

Acknowledgement

This work was supported by JSPS Grants-in-Aid for Scientific Research (A) 22255012.

th
References

JICA (Japan International Cooperation Agency). 2007. The Study on Countermeasures for Sedimentation in the
Wonogiri Multipurpose Dam Reservoir in the Republic of Indonesia. Japan International Cooperation
Agency.
Leontief, W. 1986. Input-Output Economics, 2
nd
. ed., Oxford Univ. Press.

th
Permutation Test in Evaluating the Significance of Plants in PLS-DA Model
of Jamu Ingredients

Farit Mochamad Afendi
a, b*
, Md. Altaf-Ul-Amin
a
, and Shigehiko Kanaya
a

a
Graduate School of Information Science, Nara Institute of Science and Technology, Nara, Japan
b
Department of Statistics, Bogor Agricultural University, Bogor, Indonesia
* Corresponding author: Graduate School of Information Science, Nara Institute of Science and Technology,
Ikoma, Nara 630-0101, Japan.
Tel.: +81-743-72-5952; fax: +81-743-72-5953.
[email protected]

Abstract

PLS-DA (Partial Least Square Discriminant Analysis) model is used to establish relationship between Jamu
ingredients, i.e. plants composition in Jamu, and Jamu efficacy to investigate which plants act as main
ingredients and which are supporting by checking the plants significance. Permutation testing is used in the
investigation by generating the coefficients distribution under null hypothesis, i.e. the plants are not affecting
Jamu efficacy. The generation process is performed by permuting the order of the response while maintaining
the order of the predictors. The PLS-DA model then is applied to the new dataset after permutation. After
repeating this process many times, then the accumulation of the PLS-DA coefficients provides the distribution
under the null hypothesis. The proportion of the coefficients larger than or equal to the PLS-DA coefficient using
original data then serves as the p-value, which then can be compared to the significance level o. By performing
this permutation process 1000 times and o = 5%, we found, over all efficacies, 231 out of 465 plants are
significant. Moreover, from literature review, among these 231 plants, the usages of 226 plants on the assigned
efficacy are supported by scientific paper.

Keywords: jamu, PLS-DA, permutation test

Introduction

Jamu is an Indonesian herbal medicine made from a mixture of several plants. So, the
ingredients, i.e. plants composition used, in Jamu determine the Jamu efficacy. Among the
ingredients of Jamu are plants used as main ingredients, which contribute primarily to its efficacy,
as well as plants used as supporting ingredients (Pramono, 2007; Redaksi Trubus, 2009).
Investigating which plants are main ingredients and which are supporting is important to
comprehensively understand the mechanism of plants used in Jamu to achieve specific efficacies.
A statistical model can be helpful in this attempt by relating plants usage in Jamu as predictors and
Jamu efficacy as response. Plants perform as main ingredients will have significant effect on the
model developed.
PLS-DA, a statistical model for classification and discrimination that based on Partial Least
Square Regression (PLSR) in which the dependent variable is chosen to represent class
membership (Barker and Rayens, 2003), is suitable for this analysis regarding that large number of
plants are used in Jamu and; on the other hand, Jamu efficacy are in categorical scale. Hence, the
PLS-DA coefficients can be used to explore the relationship between plants and Jamu efficacy.
Furthermore, the absence of significance testing on PLS-DA coefficients is replaced by permutation
testing, which generated the coefficients distribution under null hypothesis through resampling of
the existing data (Good, 2005).

th

Dataset
The data used in the present study are the commercial Jamu registered at The National
Agency for Drug and Food Control (NA-DFC) of Indonesia. The data contain 3138 Jamu and in total
they use 465 plants. Each Jamu is classified into one of nine efficacy categories, namely: (1) urinary
related problems (URI), (2) disorders of appetite (DOA), (3) disorders of mood and behavior (DMB),
(4) gastrointestinal disorders (GST), (4) female reproductive organ problems (FML), (6)
musculoskeletal and connective tissue disorders (MSC), (7) pain/inflammation (PIN), (8) respiratory
disease (RSP), and (9) wounds and skin infections (WND).
In the present study, the plants usage in each Jamu provides the predictors in PLS-DA
model while the Jamu efficacy serves as the responses. Let X
ij
(i = 1, 2, , n; j = 1, 2, , m; n =
3138; m = 465) denotes the status of plant j usage in Jamu i, where X
ij
= 1 if Jamu i use plant j and
0 otherwise, and let Y
ik
(k = 1, 2, , 9) denotes the efficacy status of Jamu i, where Y
ik
= 1 if Jamu i
has efficacy in category k and 0 otherwise. Note that E
k
Y
ik
= 1 meaning that each Jamu is
classified into one efficacy category only.

PLS-DA Modeling
The details of the PLS-DA modeling are as follows (Barker and Rayens, 2003; Wold et al,
2001). Let T (n x c) is a matrix of the underlying factors of X and is obtained by maximizing its
covariance with the corresponding matrix of the underlying factors of Y, that is
T = XW (1)
where W (m x c) is a matrix of weight, and c is the number of factors extracted. Matrix T, multiplied
by matrix of Xloadings P (m x c), is a good summaries of X
X = TP
t
+ E (2)
so that the Xresiduals E (n x m) is small. In addition, matrix T also a good predictors of Y
Y = TQ
t
+ F (3)
where Q (9 x c) is matrix of Yloadings. The Yresiduals F (n x 9) express the deviation between
the observed and the predicted responses.
Substituting Eq. (1) into Eq. (3) we obtain multiple regression model of PLSDA
Y = XWQ
t
+ F = XB + F (4)
where the PLS-DA coefficient matrix B (m x 9) is calculated as
B = WQ
t
(5)
Note that each plant has a set of coefficient containing 9 values, one for each efficacy.

Permutation Test in PLS-DA Model
Permutation testing is a resampling method intended to provide underlying distribution of
test statistic under null hypothesis, which then can be used to calculate p value. Unlike the
conventional statistical testing, which assuming the null distribution follows some theoretical
distribution, the permutation testing provides the null distribution by an empirical distribution which
generated through resampling of the data sample at hand. The idea of permutation testing in PLS-
DA is illustrated in Figure 3. The details of the steps are as follows.
Step 1. Resampling of Jamu data.
In this step, new Jamu data set under null hypothesis, i.e. plants are not affecting the Jamu
efficacy, is generated by resampling the existing Jamu data set. The resampling process is
performed by permuting the order of the response randomly while maintaining the order of
the predictors. This process ensures the relationship between the predictors and the
response, if any, in the original Jamu data set is destroyed. Thus, the result from this
resampling is the new Jamu data set under null hypothesis. Let denotes the new
response obtained from the permutation process.
Step 2. PLS-DA modeling on the new jamu data set.
th
PLS-DA model is performed on the new Jamu data set obtained from Step 1. The matrix X
and provide the predictors and responses, respectively. The coefficient matrix obtained
is denoted by .
Step 3. Accumulation of PLS-DA coefficients
After all permutation rounds R (in the present study we performed R = 1000 times), the
PLS-DA coefficient in each round
r
is accumulated into coefficient distribution C, which is
the distribution of PLS-DA coefficient under null hypothesis. Let C
jk,r
denotes the coefficient
of plant j on efficacy k at permutation round r.

After the distribution of PLS-DA coefficient under null hypothesis is obtained, the p value in
testing the effect of plant j on efficacy k is calculated as the following. Note that the hypothesis to be
tested is.

H
0
: |
jk
s 0 vs H
1
: |
jk
> 0.
Thus, the p value is calculated as
(6)

where is an identity function that equal to 1 if the argument is fulfilled and equal to
0 otherwise. Basically, the p value is the proportion of the coefficients larger than or equal to the
PLS-DA coefficient using original data. The null hypothesis is rejected if the p value is smaller than
the significance level o.

Figure 3. The schematic diagram of the permutation steps used in the present study.

Yes
Determination of iteration number R
r = 0
Step 1: Creating new dataset by permuting the order of the response while
maintaining the order of the predictors
Step 2: a. PLS-DA modeling on new dataset
b. Calculating PLS-DA coefficients
Increment of r
Step 3: Accumulation of PLS-DA coefficients
r s R
No
th

In the present study, in selecting the number of components used in PLS-DA, we
performed 5-folds cross validation as follows. The Jamu data set are splitted randomly into five sets.
In each round, we combined four sets as training set and the other one as testing set. We apply
PLS-DA with number of components q on training set and use the model to predict the responses of
the testing set. The PLS-DA is applied once more by selecting another four sets as training set and
the other one as testing set. After each set is once selected as testing set, the whole process is
repeated using number of components q + 1.
Prediction Error Sum of Square (PRESS) using number of components q for efficacy group
k is calculated as:

where denotes the prediction of the efficacy k for Jamu i using the PLS-DA model
obtained without Jamu i, i.e. i is within the testing data, and using number of components q. The
plot of this statistic against number of component q is shown in Figure 4. The plots are almost
constant starting from q = 10 onward for all nine efficacy groups. Thus, the number of components
of PLS-DA model for the original Jamu data set (and also for all 1000 permutation rounds) is set to
10. Analyzing PLSDA using 10 components on the original Jamu data set, we obtain the percent
variation accounted for predictors and responses are equal to 5.5% and 40.5%, respectively.

Figure 4. PRESS plot of 5fold crossvalidation.

Figure 5 gives illustration of the coefficient distribution under null hypothesis obtained from
the permutation process. In this illustration, both plants are evaluated due to their usage for Jamu
that useful for efficacy URI. The mean of the two distributions (and also for all other distributions)
are very close to 0, as expected, indicating that the distributions are generated under null
hypothesis. The normal curves were sketched on both distributions to show that not all permutation
distributions can be approached with normal distribution. This result supports the p value calculation
using empirical distribution as formulated in Eq (6). Using significance level o = 5%, we can
conclude that Phellodendron chinense is significantly affecting the Jamu efficacy URI, whereas
Foeniculum vulgare is not.
th
The results of the significancy testing of all plants used in each efficacy are shown in Table
1. Note that one plant may be used for more than one efficacy. From the testing, we observed 234
plants (50.3% among all 465 plants) showing no significant status for all 9 efficacies; whereas the
other 231 plants have significant status which comprise of 189 plants (40.6%) are significant only
for 1 efficacy, 38 plants (8.2%) are significant for 2 efficacies, and the other 4 plants (0.9%) are
significant for 3 efficacies.
Besides testing the plants usage statistically, furthermore, we also check from scientific
paper the usage of significant plants on their corresponding efficacy. The results are shown in Table
1. We obtained that most of the testing results are supported by scientific paper.

Figure 5. Illustration of the coefficient distribution under null hypothesis obtained using permutation process.

Table 1. The number of significant plants resulting from permutation testing and their support status from
scientific papers

Efficacy
Number of plants used in the
corresponding efficacy
Significant plants
Total Support from scientific paper
URI 80 20 19 (95.0%)
DOA 148 21 21 (100.0%)
DMB 47 12 11 (91.7%)
GST 290 26 26 (100.0%)
FML 182 40 39 (97.5%)
MSC 270 40 39 (97.5%)
PIN 183 39 38 (97.4%)
RSP 105 36 35 (97.2%)
WND 120 43 43 (100.0%)

Conclusion

PLS-DA model is used to establish relationship between plants composition in Jamu and
Jamu efficacy to investigate which plants act as main ingredients and which are supporting by
checking the plants significance. Permutation testing is used in the testing by generating the
coefficients distribution under null hypothesis from which p value is calculated and then compared
with significance level o. By performing this permutation process 1000 times and o = 5%, we found,
th
over all efficacies, 231 out of 465 plants are significant. Moreover, from literature review, among
these 231 plants, the usages of 226 plants on the assigned efficacy are supported by scientific
paper.

References

Barker M, and W Rayens. 2003 Partial least squares for discrimination. J. Chemometrics. 17: 166-173
Good PI. 2005. Permutation, Parametric and Bootstrap Tests of Hypotheses, 3
rd
ed. Springer, New York
Pramono S. 2007. Jamu in Indonesian Daily Life and Industry. Institute of Natural Medicine, University of
Toyama, Toyama
Redaksi Trubus. 2009. Herbal Indonesia Berkhasiat: Bukti Ilmiah dan Cara Racik. PT Trubus Swadaya, Depok
Wold S, M Sjstrm, and L Eriksson. 2001. PLS-regression: a basic tool of chemometrics. Chemometrics and
Intelligent Laboratory Systems, 58: 109-130

th
Index of Authors

A Junaedi, 175
Abdul Munif, 315
Ade Noverta, 380
Agus Rachmat, 91
Agus Sutanto, 291
Ahmad Denian, 380
Ahmad Ghozi Mansyuri, 225
Akihiko Kamoshita, 19
Akihiro Fujii, 239
Akihiro Kishikawa, 235
Akiho Yokota, 1, 296, 401
Akira Miyazaki, 107
Akira Yamauchi, 51,153, 334
Alhassan I Zakaria, 29
Ali Asgar, 249, 269
Alia Astuti, 220
Amol Dahal, 56
Anischan Gani, 72
Arief Sabdo Yuwono, 410
Aries Kusumawati, 225
Asadi, 180, 209
Asma Sembiring, 274
Asuka Yamano, 343
Atsushi Kato, 296
Atsushi Nakagawa, 14
Atsushi Yoshimura, 34
Azmi Dhalimi, 380
Baiq Nurul Hidayah, 282
Bambang Pujiasmanto, 324
Bambang Sapto Purwoko, 39, 45, 80, 85
Bayu D A Nugroho, 416
Bernadetta Rina Hastilestari, 91
Boonrat Jongdee, 61
Candra Catur Nugroho, 141
Catur Hermanto, 291
Chairunas, 72
Chiharu Hongo, 96
Chiharu Sone, 24
Chihiro Shimada, 14
Chika Nakashima, 14
Chojiro Kojima, 14
D Sagala, 175
Darman M Arsyad 180, 209
Darmono Taniwiryono, 389
Deni D Sulaeman, 80
Desta Wirnas, 80, 85
Dewi Indriyani Roslim, 130
Dewi Sukma, 291
Dhika Amanda, 353
Dina RR, 287
Dwi Praptomo Sudjatmiko, 282
Eiji Tanesaka, 235
Elis N Herliyana, 389
Elizabeth Caroline Situmorang, 370, 358
Elly Kesumawati, 66
Ence Darmo Jaya Supena, 220
Endang Yuniastuti, 244
ER Aweng, 405
Eri Sofiari, 274
Eriko Hayashi, 153
Erita Hayati, 66
Ernawati Giri R, 287
Fadlilla Dewi Rakhmawaty, 13
Farit Mochamad Afendi, 427
Futoshi Kato, 125, 252, 262
Futoshi Sasaki, 125, 252
Gunardi Sigit, 96
H Aswidinnoor, 39
Hai Yan, 196
Hamda Fauza, 380
Handarto, 96
Happy Widiastuti, 364, 375
Haruka Yamaguchi, 215
Hayati Minarsih, 389
Hayuru Yoshida, 279
Heni Purnamawati, 225
Heni Safitri, 80, 85
Hiroaki Shirakawa, 96
Hiroki Iwamoto, 96
Hiroki Suto, 279
Hiromitsu Kanno, 416
Hiroshi Ehara, 5, 159
Hiroshi Fujii, 416
Hirotake Itoh, 230
Hiroyuki Tsuji, 14
Hitoshi Naito, 5, 159
Hitoshi Sato, 230
Hozumi Yoshida, 230
Ima MZ, 287
Indrastuti A Rumanti, 39
th
Indrawan A, 385
Irdika Mansur, 385
Irfan K Putra, 389
Irfan Martiansyah, 130
Iskandar Lubis, 225
Istino Ferita, 380
Iswari S Dewi, 39, 45, 80, 85
Izuru Ohki, 14
J Nulik, Nurhayati, 331
Jaladet MS Jubrael, 395
Jamsari, 380
Jing Ju, 107
Jonathan M Niones, 51
Jose MA Ornai, 85
Julie M Warren, 282
Jun-Ichi Sakagami, 24, 29
Kalimatul Jumro, 185
Kazuo Oki, 96
Kei Kajisa, 119
Keiichi Hayashi, 29
Kei-ichiro Maeda, 334
Keisuke Katsura, 191, 205
Keita Nabeya, 165
Keitaro Watanabe, 76
Ken-ichiro Taoka, 14
Kentaro Kawaguchi, 147
Khairun Nisa, 72
Kinasih Prayuni, 91
Kinya Akashi, 296
Kiyoshi Fujii, 153
Ko Shimamoto, 14
Kohtaro Isek,i 61
Koki Homma, 61, 96, 101, 191
Kokoro Hayashi, 14
Koshi Yoshida, 96
Koutarou Mori, 343
Kyoko Furuita, 14
Kyoko Takahashi, 279
L Abdullah, 331
Lailatul B, 287
Larry C Purcell, 191
Larry CM Lopez, 416
Lia Hadiawati, 282
Lizah Khairani, 339
M Ghulamahdi, 175
M Karimah, 405
Maya Melati, 175 185
Makara Ouk, 19
Makie Kokubun, 196
Malem McLeod, 72
Manabu Watanabe, 165
Mari Iwaya-Inoue, 215
Mariko Nakagawa, 348
Marlin Sefrila, 137
Masao Sato, 34
Masayasu Maki, 96
Masayuki Murai, 56
Mathias Fosu, 29
Md. Altaf-Ul-Amin, 427
Michihiko Fujii, 113
Michio Kawasaki, 279
Midori Yamaguchi, 14
Miftahudin, 130
Mika Yoshinaga, 334
Mikio Sekinuma, 125, 252
Mitsuo Kambayashi, 96
Mitsuo Kuwada, 101
Mitsuo Saito, 239
Mochamad Arief Soleh, 196
Morio Matsuzaki, 305
Motonobu Yoshida, 235
Muhafaz Zulusfitri, 66
Muhamad Syukur, 80
Muhammad Syafii, 45
Munandar, 137
Munif Ghulamahdi, 225
Murdaningsih H Karmana, 380
Mutsumi Akama, 165
Nadar Khan, 348
Naoto Inoue, 125, 252, 262
Naoya Nakamura, 401
Naoyoshi Kawano, 24
Narasimham Upadyayula, 11
Nguyen TB Yen, 19
Nurul Khumaida, 141
Ohn Mar Khin, 34
OR Nahak, 331
Ornprapa Anugoolprasert, 159
Osuhaini, 405
Paul PS Teng, 15
PDMH Karti, 331
Peter Dawson, 282
Peter Slavich, 72
Prijanto Pamoengkas, 385
Putri DU, 287
PV Vara Prasad, 2
R Kirana, 256
Raed A Haleem, 395
th
Randall L Nelson, 191
Renih Hayati, 137
Renny Fatmyah Utamy, 343, 339
Rika Fithri Buana, 358, 370
Rita Harni, 315
Ritsuko Hara, 96, 101
Rochadi Abdulhadi, 310
Rudiyanto, 319
Ryohta Shinohara, 113
Ryoji Sameshima, 196, 416
Ryuji Yoshida, 76
S Nofyangtri, 331
Sabaruddin, 137
Sachiko Idota, 339, 343
Sahuri, 175
Saki Hoshiyasu, 296
Samanhudi, 324
Samir K Abdullah, 395
Sandra Arifin Aziz, 175, 200
Satoko Yasumoto, 305
Satomi Sakazono, 169
Satoshi Nakamura, 165, 239
Satoshi Shimamura, 169
Satoshi Uchida, 421
Satya Nugroho, 91
Sayuri Kajihara, 169
Seiji Ishihara, 113
Seishi Yoshida, 262
Seito Hosokawa, 279
Shao-Hui Zheng, 215
Shigehiko Kanaya, 427
Shigeki Yokoyama, 119, 421
Shigeru Shigeoka, 3
Shina kinoshita, 159
Shintaro Kobayashi, 421
Shinya Kasajima, 230
Shojiro Tamaki, 14
Sintho Wahyuning Ardie, 141
Siswanto, 315
Somchai Chakhatrakan, 159
Sony Suhandono, 287, 353
Sri Astuti Rais, 225
Sri Ayu Dwi Lestari, 200
Sri Rahayu, 300, 310
ST Rahayu, 249, 256
Stanis Malangen, 56
Sudarsono, 91, 291
Sudjudi, 282
Sufardi, 72
Suharsono, 220
Susanti Indriya Wati, 244
Susumu Arima, 215
Suwarto, 141
Taiki Yoshihira, 191
Takako Tsuji, 153
Takashi Hashimoto, 12
Takashi Yuasa, 215
Takayuki Nakano, 235
Takehiro Natori, 125
Takeshi Akaoka, 56
Takumi Iwakura, 56
Takuya Koyama, 334
Tamao Hatta, 29
Tantono Subagyo, 13
Tatik Chikmawati, 130
Tatsuhiko Shiraiwa, 101
Tatsuhiko Shiraiwa, 96, 191, 205
Tatsuro Miyazaki, 119
Teiji Nakamura, 165
Terry Hill, 282
Tetsushi Yoshida, 107, 153
Tomohiro Konno, 196
Tomohito Hayashi, 153
Tomoko Yanase, 14
Tomoyuki Katsube-Tanaka, 348
Tong Li-Tao, 34
Tony Liwang, 17
Toru Hata, 56
Toshiaki Kokubo, 107
Toshihiro Mochizuki, 34, 169
Tri Muji Ermayanti, 319
U Sumpena, 249
Wahyudi, 385
Wikanya Prathumyot, 5
Wisnu Adi Wicaksono, 358, 370
Y Puspitasari, 175
Yahaya Inusah, 29
Yasuhiro Tsujimoto, 29
Yasuo Nakamaru, 230
Yasuyuki Ishii, 339, 343
Yekti Asih Purwestri, 14
Yohei Kawasaki, 191, 205
Yoshiaki Inukai, 51
Yoshihiro Hirooka, 101
Yoshihiro Hirooka, 96
Yoshiko Iizumi, 421
Yoshinori Yamamoto, 107
Youji Nitta, 165
th
Yu Tanaka, 205
Yudiwanti WE Kusumo, 225
Yuji Araki, 19
Yuji Matsue, 34
Yuka Ogaki, 14
Yukari Terakado, 305
Yukiyo Yamamoto, 29
Yulong Wang, 107
Yuri Nakajima Munekage, 401
Yurie Okada, 153
Yushi Ishibashi, 215
Yusuke Goto, 165, 239
Yusuke Takahashi, 348
Zaitun, 72

th
List of Organizing Committee

Chairman : Sony Suharsono (IPB)
Vice Chairman I : Miftahuddin (IPB)
Vice Chairman II : Bambang Purwantara (BIOTROP)
Secretary : Komang G Wiryawan (IPB)
Treasurer : Utut Widyastuti (IPB)
Secretariat : Noor Faiqoh Mardatin (IPB)
: Dewi Suryani (IndoBIC)
: Desi Maryanti (PT Paqar)
Funding : Herry Kristanto (Monsanto)
: Elisabeth Maria (PT Sentra Biosains Dinamika)
Scientific Program : Muhammad Yunus (Balitbiogen, Balitbangtan)
: Antonius Suwanto (IPB)
: Satya Nugroho (LIPI)
: Karden Mulya (Balitbiogen, Balitbangtan)
: Ence Darmo Jaya Supena (IPB)
Seminar Program : Trimuji Ermayanti (LIPI)
: Hayati Minarsih (Balit Bioteknologi Perkebunan)
: Saptowo J Pardal (Balitbiogen, Balitbangtan)
Logistic : Ahmad Junaedi (IPB)
: Trikoesoemoeningtyas (IPB)
: Syamsul Komar (IndoBIC)

th
th
List of Participants

No Name of Participant Institution
1. Abdul Munif
Faculty of Agriculture, Bogor Agricultural University,
Indonesia
2. Agus Rachmat
Research Center For Biotechnology,
Indonesian Institute of Sciences, Indonesia
3. Agus Sutanto
Department of Agronomy and Horticulture,
Bogor Agricultural University, Bogor, Indonesia
4. Ahmad Anwar Ismail University of Malaysia, Kelantan, Malaysia
5. Ahmad Rifqi Fauzi
Department of Agronomy, Faculty of Agriculture,
Universitas Negeri Papua, Indonesia
6. Akihiro Fujii
Graduate School of Agriculture, Tohoku Univ., Miyagi,
Japan
7. Akihiro Suzuki Saga University, Japan
8. Akiho Yokota Nara Institut of Science and Technology, Japan
9. Akira Yamauchi
Graduate School of Bioagricultural Science,
Nagoya University, Nagoya 464-8601, Japan
[email protected]
10. Ali Asgar
Indonesian Vegetables Research Institute
Jl. Tangkuban Perahu No. 517 Lembang 40791
Tel.(022)2786245, PO BOX 1586 Bandung, Indonesia
[email protected]
11. Alia Astuti
Department of Biology, Bogor Agricultural University,
Indonesia
12. Anggayudha Ananda Rasa
Bandung Institute of Technology (ITB), Indonesia
[email protected]
13. Anggiani Nasution
Indonesian Center for Rice Research, ICRR,
Sukamandi, Indonesia
14. Anugoolprasert Ornprapa Mie University, Japan
15. Ardha Apriyanto
School of Life and Sciences,
Bandung Institute of Technology, Bandung, Indonesia
16. Ari Susilowati
Department of Biology, Faculty of Mathematics and
Natural Sciences, University of Sebelas Maret.
Jl. Ir. Sutami No. 36A, Kentingan, Surakarta,
Indonesia 57126
17. Arief Sabdo Yuwono
Dept. of Civil and Environmental Engineering (SIL),
18. Arum Sekar Wulandari
Faculty of Forestry, Bogor Agricultural University,
Indonesia
th
19. Asma Sembiring
Indonesian Vegetable Research Institute (BALITSA)
Jl.Tangkuban Perahu No.517 Lembang,
Bandung-40395, Indonesia
Tel : +62 22786245; fax : 62 22786416
[email protected]
20. Asmini Budiani
Indonesian Biotechnology Research Institute for
Estate Crops, Bogor, ndonesia
21. Astri S Perkindo/Perkin Elmer
22. Atsushi Kato
Laboratory of Plant Development and Molecular
Morphogenesis,
Graduate School of Biological Sciences,
Nara Institute of Science and Technology (NAIST),
Nara 630-0101, Japan
23. Aweng a Mr. /l Eh Rak University of Malaysia Kelantan (UMK), Malaysia
24. Baiq Nurul Hidayah
Assessment Institute for Agricultural Technology
(AIAT)
Nusa Tenggara Barat, Indonesia
25. Bambang Pujiasmanto
Department of Agrotechnology,
Faculty of Agriculture, Sebelas Maret University,
Surakarta, Indonesia
26. Bambang Sapto Purwoko
Bogor Agricultural University, Bogor Indonesia
27. Bayu Dwi Apri Nugroho
The United Graduate School of Agricultural Sciences,
Ueda 3-18-34, Morioka, Iwate, Japan 020-8550.
Tel.: +81 19 643 3408; fax: +81 19 641 9296;
[email protected]
28. Cailin Lei
Japan International Research Center for Agricultural
Sciences (JIRCAS)
29. Cassandra Monash University, Australia
30. Cecep Bogor Agricultural University, Indonesia
31. Chengyun Li
Sciences (JIRCAS)
32. Chisato Sugiyama
Graduate school of Agriculture,
Tokyo University of Agriculture and Technology,
Fuchu, Tokyo183-8509, Japan
Tel: +81 42 367 5672; Fax: +81 42 367 5671;
[email protected]
33. Darman M Arsyad
Central Institute for Agricultural Technology
Assessment and Development, Bogor, Indonesia
34. Deddy Crop Life Indonesia
35. Dedeh Hartati Bogor Agricultural University, Indonesia
th
36. Delima H A
Center of Agricultural Research and Development,
Ministry of Agriculture, Bogor, Indonesia
37. Dewi Indriyani Roslim
Bogor, Indonesia
38. Dewi Sukma
39. Dhika Amanda
School of Science and Technology,
40. Dian Catur P PT. BISI International Tbk.
41. Dwi Praptomo
(AIAT)
42. Dwinita W Utami
The Agency of Crop Biodiversity and Genetic
Resources,
43. Elis Nina Herliyana Bogor Agricultural University, Indonesia
44. Elly Kesumawati
Faculty of Agriculture, University of Syiah Kuala,
Banda Aceh, Indonesia
45. Endang Yuniastuti
Faculty of Agriculture, Sebelas Maret University,
Indonesia
46. Endro Gunawan
47. Eri Maai
Graduate School of Bioagricultural Sciences,
Nagoya University, Aichi, Japan
48. Eries Dyah Mustikarini
Jurusan Agroteknologi FPPB, Universitas Bangka
Belitung. Balunijuk, Merawang, Bangka
Kepulauan Bangka Belitung, Indonesia
49. Etsushi Kumagai
NARO Tohoku Agricultural Research Center, 4
Akahira, Shimokuriyagawa, Morioka, Iwate 020-0198,
Japan
50. Etti Swasti
Faculty of Agriculture, Andalas University. Padang,
Indonesia
51. Eva Erdayani
Research Center for Biotechnology, Indonesian
Institute of Science, Cibinong, Indonesia
52. Fadhillah PT Pandu
53. Fadlila Dewi R Syngenta
54. Farit Mochamad Affendi
Graduate School of Information Science,
Nara Institute of Science and Technology, Ikoma,
Nara 630-0101, Japan.
Tel.: +81-743-72-5952; fax: +81-743-72-5953;
[email protected]
th
55. Fatichin
The United Graduated School of Agricultural
Sciences,
Kagoshima University, Japan
56. Futoshi Kato
Faculty of Agriculture, Shinshu University. 8304
Minamiminowa, Nagano 399-4598, Japan.
Tel.: +81 265 77 1409 ; fax: +81 265 77 1409;
[email protected]
57. Futoshi Sasaki
Interdisciplinary Graduate School of Science and
Technology, Shinshu University, Minamiminowa,
Japan
58. Hadiwiyono
Faculty of Agriculture, University of Sebelas Maret
(UNS), Surakarta
Jl. Ir. Sutami No.36A Kentingan Surakarta (57126),
Indonesia
Tel/Fax: (0274) 637457; [email protected]
59. Hamda Fauza
Faculty of Agriculture, Andalas University,
Kampus Limau Manis 25163 Padang, Indonesia
60. Happy Widiastuti
Indonesian Biotechnology Research Institute for
Estate Crops, Bogor, Indonesia
61. Haruna Tanaka Mie University, Japan
62. Hassan Y. Al Ayied
Natural Resources and Environment Research
Institute (NRERI)
63. Hayati Minarsih
Indonesian Biotechnological Research Institute for
Estate Crops, Bogor, Indonesia
64. Hiroshi Ehara
Graduate School of Bioresources, Mie University
Japan
65. Hiroshi Miyake
Nagoya University, Furo-cho, Chikusa, Nagoya, Aichi,
464-8601, Japan.
66. Hiroyuki Shimono
Faculty of Agriculture, Iwate University,
3-18-8, Ueda, Iwate, 020-8550, Japan.
Tel.: +81 19 621 6146; fax: +81 19 621 6146;
[email protected]
67. Hiroyuki Tsuji
Laboratory of Plant Molecular Genetics,
Nara Institute of Science and Technology, Japan
68. Indrastuti Apri Rumanti
Indonesian Center for Rice Research (BB Padi)
Jl Raya 9 Sukamandi, Indonesia
69. Inez HS Loedin
Research Center for Biotechnology, Indonesian
Institute of Science, Bogor, Indonesia
And
IRRI Manila, Philippine
70. Iskandar Lubis
Department of Agronomy and Horticulture, Bogor
Agricultural University, Bogor, Indonesia
71. Iswari S Dewi
ICABIOGRAD
Jl. Tentara Pelajar no 10A Bogor, Indonesia
[email protected]
72. Jinbin Li
Sciences (JIRCAS)
th
73. Jonathan Niones Nagoya University, Japan
74. Jose Maria AO Bogor Agricutural University, Indonesia
75. Jun-ichi Sakagami
Sciences (JIRCAS)
76. Kazunobu Toriyama
Sciences (JIRCAS)
77. Keisuke Katsura
Graduate School of Agriculture, Kyoto University,
Japan
78. Kentaro Kawaguchi
National Agriculture and Food Research Organization
(NARO)
79. Khay Sathya
Sciences (JIRCAS)
80. Kohtaro Iseki
Kyoto, Japan
81. Koki Homma
Kyoto, Japan
82. Kulvinder S Gill
Department of Crop and Soil Science, Washington
State University
83. Kuniyuki Saitoh
Graduate School of Natural Science and Technology,
Okayama University, Okayama, Japan
84. Kustiariyah
Faculty of Fisheries & Marine Sciences,
Bogor Agricultural University, Indonesia
85. Lailatul Badriyah
School of Life and Sciences,
86. Latifah K Darusman Biofarmaka, Bogor Agricultural University, Indonesia
87. Lia Hadiawati
(AIAT)
88. Loida M Perez
Sciences (JIRCAS)
89. Mai Goto
Graduate School of Agriculture,
Fuchu, Tokyo, Japan
90. Maya Melati
91. Md. Ansar Ali
Sciences (JIRCAS)
92. Michihiko Fujii Faculty of Education, Shizuoka University, Japan
th
93. Michio Kawasaki
Faculty of Agriculture and Life Science,
Hirosaki University, Aomori, Japan
94. Miftahudin
Bogor, Indonesia
95. Mikio Nakazono
Nagoya University, Japan
96. Mikio Sekimuna
Interdisciplinary Graduate school of Science and
Technology,
Shinshu University, Japan
97. Mituhiro Obara
Sciences (JIRCAS)
98. Mochamad Arief Soleh
Graduate School of Agricultural Science,
Tohoku University, Japan
99. Motonobu Yoshida
Dept of Agricultural Science, Kinki University,
Nakamachi 3327-204, Nara, Japan
100. Muhammad Addip Novianto BMKG
101. Muhammad Syafii Bogor Agricultural University, Bogor, Indonesia
102. Muhammad Yunus
The Agency of Crop Biodiversity and Genetic
Resources,
103. Munif Ghulamahdi
104. Nagao Hayashi
Sciences (JIRCAS)
105. Naomi Asagi Ibaraki University, Japan
106. Naoya Nakamura
Graduate school of Biological Sciences,
Ikoma, Nara 630-0101, Japan
107. Narasimham Upadyayula Monsanto Singapore Co (Pte) Ltd Singapore
108. Nguyen Thi Bich Yen
Asian Natural Environmental Science Center,
The University of Tokyo, Japan
109. Nguyen Thi Lang
Sciences (JIRCAS)
110. Nguyen Thi Thanh Thuy
Sciences (JIRCAS)
111. Nguyen Van Kien
Division of Genebank Management,
Plant Resources Center
An Khanh, Hoai Duc, Ha Noi, Vietnam
112. Niken TM Pratiwi
th
113. Niken Trisnaningrum PT. BISI International Tbk.
114. Nishe Fransiska Bogor Agricutural University, Indonesia
115. Nobuhiro Noda
Mie university
[email protected]
514-8507 Mie, Tsu-shi, 1577 Kurimamachiya-cho
116. Nurliani Bermawie BALITTRO Bogor, Indonesia
117. Nurul Khumaida
118. Ohn Mar Khin Faculty of Agriculture, Kyushu Univ., Fukuoka, Japan
119. Panca Dewi Manu Hara Karti
Faculty of Animal Husbandry,
120. Paul PS Teng
National Institute of Education,
Nanyang Technological University, SIngapore
121. Phoumi Inthapaya
Sciences (JIRCAS)
122. Poonsak Mekwatanakarn
Sciences (JIRCAS)
123. PV Vara Prasad
Department of Agronomy, Kansas State University,
Manhattan, Kansas 66506, USA
124. Raed A Haleem
University of Duhok (UoD),
Faculty of Agriculture and Forestry,
Kurdistan region, Iraq
125. Rahmat H
CENTRAS, LPPM, Bogor Agricultural University,
Indonesia
126. Randy Hautea
SEAsia Center Director and ISAAA Global
Coordinator
International Service for the Acquisition of Agri-
biotech Applications (ISAAA)
127. Renih Hayati
Fac. of Agriculture, Sriwijaya University, Palembang,
Indonesia
128. Renny Fatmyah Utamy Faculty of Agriculture, University of Miyazaki, Japan
129. Retno Lestari Universitas Indonesia
130. Rika Fithri Nurani B PT SMART Tbk.
131. Rika Raffiudin
Bogor, Indonesia
132. Rinda Kirana Institution Vegetables Research (IVEGRI), Indonesia
th
133. Ritsuko Hara
Japan
134. Rudiyanto
Research Center for Biotechnology , Indonesian
135. Rujito Agus Suwignyo
Faculty of Agriculture, Sriwijaya University,
Palembang, Indonesia
136. Ruth Martha Winnie Bogor Agricultural University, Bogor, Indonesia
137. Samanhudi
Department of Agrotechnology,
Faculty of Agriculture, Sebelas Maret University
Jl. Ir. Sutami 36A, Surakarta, Indonesia 57126
138. Sandra Arifin Aziz
139. Santoso
Indonesian Center for Rice Research,
Jln Raya 9, Sukamandi, Subang 41256, West Java,
Indonesia

140. Sara PT ITS
141. Satoko Yasumoto
Biomass Production and Processing Research Team,
Production Systems Research Area,
National Agricultural Research Center Tsukuba,
Japan
142. Satoshi Nakamura
School of Food, Agricultural and Environmental
Sciences,
Miyagi University, Sendai, Miyagi, Japan
143. Satriyas Ilyas
Faculty of Agriculture,
144. Shao-Hui Zheng
Coastal Bioenvironment Center, Saga University,
Karatsu, Saga 840-0021, Japan
145. Shigeki Yokoyama
Sciences (JIRCAS)
146. Shigeru Shigeoka
Department of Advanced Bioscience,
Faculty of Agriculture, Kinki University, Japan
147. Shinsuke Kasa
Graduate School of Bioresourches and
Bioenvironmental Science, Kyushu University, Japan
148. Shintaro Kobayashi
Sciences, Tsukuba, Japan
149.
Shinya Kasajima

Faculty of Bioindustry, Tokyo University of Agriculture,
Hokkaido, Japan
150. Shiro Mitsuya
Nagoya University, Nagoya, Japan
151. Shunsuke Adachi
Japan
152. Sintho Wahyuning Ardie
th
153. Sobir Bogor Agricultural University
154. Sony Suhandono
School of Life and Sciences, Bandung Institute of
Technology, Bandung, Indonesia
155. Sri Rahayu
Bogor Botanical Gardens,
Indonesian Institute of Sciences, Bogor, Indonesia
156. Stanis Malangen
United Graduate School of Ehime University,
Matsuyama, Ehime, 790-8566, Japan
157. Suharsono
Bogor, Indonesia
158. Sulandjari
Faculty of Agriculture , Sebelas Maret University,
Surakarta, Indonesia
159. Suliman Ali Al-Khateeb
Environment and natural resources Department,
King Faisal University, Kingdom of Saudi Arabia.
P.O.Box 420, Alhofof 31982.
[email protected]
160. Supijatno
161. Susumu Arima
Faculty of Agriculture, Saga University,
Saga 840-8502, Japan
162. Suwarni Tri Rahayu Institution Vegetables Research (IVEGRI) Indonesia
163. Suwarno
Indonesian Center for Rice Research,
Jln Raya 9, Sukamandi, Subang 41256, West Java,
Indonesia

164. Tadashi Hirasawa
Japan
165. Tadashi Sato
Sciences (JIRCAS)
166. Taiichiro Ookawa
Japan
167. Takao Oi
Nagoya University, Aich, Japan
168. Takashi Homma
The College of Agricuture, Ibaraki University,
3-21-1, Ami, Ibaraki 300-0393, Japan
Tel: +81 29 888 8556; fax: +81 29 888 8556
[email protected]
169. Takasi Hashimoto
Graduate School of Biological Science,
Nara Institute of Science and Technology, Japan
170. Takehiro Mukouyama
Japan
171. Takeshi Kano
Sciences (JIRCAS)

th
172. Takunari Kono
Graduate school of Biological Sciences,
Ikoma, Nara 630-0101, Japan
173. Takuya Koyama
Department of Biosphere Resources Science,
Nagoya University, Nagoya, Japan
174. Tantono Subagyo
Syngenta Indonesia, Perkantoran Hijau Arkadia,
Tower C, 8
th
fl, Jakarta
175. Tati Kristianti
School of Science and Technology,
176. Thelma F Padolina
Sciences (JIRCAS)
177. Titi Rahayu USA Embassy, Jakarta
178. Tito Deski PBS, IFPRI
179. Tohru Kobata
Faculty of Life and Environmental Science,
Shimane University, 1060 Nishikawatsu-cho,
Matsue, 690-8504, Japan
180. Tomohito Hayasi
Graduate School of Bioagricultural Sciences Nagoya
University, Nagoya, Japan
181. Tomomi Abiko
Sciences (JIRCAS)
182. Tomoyuki Katsube-Tanaka
Kitashirakawa, Kyoto 606-8502, Japan
183. Tony Liwang
Plant Production and Biotechnology Division,
PT SMART Tbk, BII Plaza Tower 2, 10
th
floor.
Jl. MH Thamrin 51 Jakarta, Indonesia
184. Toshiaki Kokubo
United Graduate School of Agricultural Sciences,
Ehime University, Japan
185. Toshihiro Mochizuki Faculty of Agriculture, Kyushu University, Japan
186. Toshiki Yamamoto Mie University, Japan
187. Totok Hesterianoto
188. Tri Lestari
University of Bangka Belitung, Bangka Belitung,
Indonesia
189. Tri Muji Ermayanti
Research Center For Biotechnology, Indonesian
190. Tsutomu Ishimaru
Sciences (JIRCAS)
191. Utut Widyastuti
Bogor, Indonesia
th
192. Wahyudi
Department of Forestry, Palangka Raya University,
Palangka Raya, Indonesia
193. Wisnu Adi Wicaksono PT SMART Tbk
194. Woro Umayi Ananda Syngenta
195. Xin Zhao
The United Graduated School of Agricultural
Sciences,
Kagoshima University, Japan
196. Yasuhiro Tsujimoto
Sciences (JIRCAS)
197. Yasumoto Satoko
Biomass Production and Processing Research Team,
Production Systems Research Area,
National Agricultural Research Center Tsukuba,
Japan
198. Yasuyuki Ishii Faculty of Agriculture, University of Miyazaki, Japan
199. Yohei Kawasaki
Japan
200. Yohei Koide
Sciences (JIRCAS)
201. Yoshihiro Nishihara Faculty of Agriculture, Saga University, Saga, Japan
202. Yoshimichi Fukuta
Sciences (JIRCAS)
203. Youji Nitta Ibaraki University 300-0393 Japan
204. Yudiwanti Wahyu E Kusumo
205. Yukari Isobe
The Colledge of Agriculture, Ibaraki University, Ami,
Ibaraki, Japan
206. Yushi Ishibashi
Crop Science Lab., Faculty of Agriculture, Kyushu
University, Hakozaki, Fukuoka 812-8581, Japan
207. Zaitun
Faculty of Agriculture, University of Syiah Kuala,
Banda Aceh, Indonesia

th

th
List of Organizers

th
th
Acknowledgements

th
th

th
th

Proceeding ACSAC ISBN PDF

Uploaded by

Copyright:

Available Formats

Proceeding ACSAC ISBN PDF

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Proceeding ACSAC ISBN PDF

Uploaded by

Copyright:

Available Formats

The 7

100 type, Chisso Asahi Fertilizer Co., Ltd. (about 7% of each

100 type six days after transplanting. In additional to 4.0 g/m

Cosmo Oil Co., Ltd., Japan

59-year 6-year None Basal Conv.

Days after treatment

treated leaves, especially at 4 and 6 DAT (Fig. 3A).

3100-Avant Genetic Analyzer (Applied Biosystems) using BigDye

Plant ength (cm)

Root dry weight (g D.W. plant

Disk diameter (cm)

1 plant m-2 4 plants m-2 8 plants m-2

1 plant m-2 4 plants m-2 8 plants m-2

Plant density (plants m

Solution Kit (Sigma, USA), followed by cDNA

You might also like