Emergent Properties of Individual Organisms
Emergent Properties of Individual Organisms
Emergent Properties of Individual Organisms
of Individual Organisms
Emergent Properties
of Individual Organisms
10 9 8 7 6 5 4 3 2 1
Keywords
fungus, superorganism, behaviors, natural selection, fight-or-flight, divi-
sion of labor, dominance hierarchy, subordinate, fear, anger, individual,
colony, physiological response, endocrine system, nervous system, coop-
eration, mutual benefit
Contents
Preface...................................................................................................ix
Acknowledgments....................................................................................xi
Introduction.........................................................................................xiii
Chapter 1 The Definition of the Individual Can Be Stretched
Beyond the Classic Definition1
Chapter 2 The Nervous and Endocrine Systems Are the Sources
of Emotions.....................................................................17
Ethical, Legal, Social Implications: There Are Issues
With Using Prescription Drugs to Normalize
Behavior in Children26
Chapter 3 Individuals of Some Species Cooperate With Each
Other for Mutual Benefit.................................................29
Conclusion............................................................................................43
Glossary................................................................................................45
Index....................................................................................................47
Preface
This book about emergent properties of individual organisms is part of
a thirty book series that collectively surveys all of the major themes in
biology. Rather than just present information as a collection of facts, the
reader is treated more like a scientist, which means the data behind the
major themes are presented. Reading any of the thirty books by Paradise
and Campbell provides readers with biological context and comprehen-
sive perspective so that readers can learn important information from a
single book with the potential to see how the major themes span all size
scales: molecular, cellular, organismal, population and ecologic systems.
The major themes of biology encapsulate the entire discipline: informa-
tion, evolution, cells, homeostasis and emergent properties.
In the twentieth century, biology was taught with a heavy emphasis
on long lists of terms and many specific details. All of these details were
presented in a way that obscured a more comprehensive understanding.
In this book, readers will learn about emergent properties of individu-
als and some of the supporting evidence behind our understanding. The
historic and more recent experiments and data will be explored. Instead
of believing or simply accepting information, readers of this book will
learn about the science behind emergent properties of individuals the
way professional scientists dowith experimentation and data analysis.
In short, data are put back into the teaching of biological sciences.
Readers of this book who wish to see the textbook version of this
content can go to www.bio.davidson.edu/icb where they will find
pedagogically-designed and interactive Integrating Concepts in Biology
for introductory biology college courses or a high school AP Biology
course.
Acknowledgments
Publishing this book would not have been possible without the generous
gift of Dr. David Botstein who shared some of his Breakthrough Prize
with co-author AMC. Davids gift allowed us to hire talented artists (Tom
Webster and his staff at Lineworks, Inc.) and copyeditor Laura Loveall.
Thanks go to Kristen Mandava of Mandava Editorial Services for project
management and guidance. In particular, we are indebted to Katie Noble
and Melissa Hayban for their many hours and attention to detail.
Kristen Eshleman, Paul Brantley, Bill Hatfield and Olivia Booker
helped us with technology at Davidson College. We are grateful to ad-
ministrators Tom Ross, Clark Ross, Carol Quillen, Wendy Raymond,
Verna Case, and Barbara Lom who had confidence in us and encouraged
us to persist despite setbacks along the way.
Thanks to my wife Amy Brooks for her constant support during the
development of this textbook, and my daughter Evelyn for her endless
energy. Thanks to Malcolm Campbell for his steadfast resolve and opti-
mism. Without him, this book would not exist. Thanks to collaborator
Laurie Heyer for taking my sometimes half-baked math ideas and turn-
ing them into powerful and elegant Bio-Math Explorations. I learned a
lot from both of them. While the math is largely absent from this book,
our collaboration with her made this a better book. Nancy Stamp at
Binghamton University, and Bill Dunson and Richard Cyr at The
Pennsylvania State University influenced me greatly in how I think as
a scientist and approach my teaching. Finally, I thank my students in
Integrated Concepts in Biology II, who enthusiastically participated in
our experiment to redesign introductory biology, starting with the text
and ending with a new approach to teaching biology.
Introduction
Ren Descartess famous quote, I think, therefore I am, is a powerful
statement on emergent properties. A human exists because they have
consciousness and can think. The human brain can be described in terms
of cellular functions and biochemical reactions. Yet describing the brain
does not explain the emergent property of human consciousness. Brains
perform at a level that exceeds the functions of individual neurons. Truly,
who could have predicted that consciousness would arise from all the
components that make up the human brain? Many other aspects of in-
dividuals, including the individual itself, can be considered emergent
properties.
In this book, several ideas about properties of individuals that lead
to emergence of new and unpredictable properties will be explored. In
the first chapter, in line with Descartes, the definition of the individual
will be contemplated, especially in cases when the lines of individuals
are blurred. The second chapter addresses a topic very familiar in daily
life but rarely studied in biology classes. Data will be used to help un-
derstand the biological origins of emotions. The final chapter explores
another topic debated by biologists, which is the conditions under which
organisms cooperate with each other.
CHAPTER 1
the honey mushroom. One of their goals was to determine the size lim-
its of individuals. This species of fungus, like many others, is a decom-
poser and survives on wood. Anderson and his colleagues sampled for the
fungus in a forest. To understand the results of the study, it is helpful to
know a few things about fungi. Many fungi live in the soil and are only
noticed when they produce fruiting bodies, also known as mushrooms
(Figure 1A). Mushrooms are the enlarged aboveground fleshy fruiting body
of certain types of fungi. The part that lives underground is composed of
microscopic thread-like structures called hyphae (Figure 1B). The branch-
ing growth pattern of hyphae leads to development of a mycelium, which
is an interconnected network of hyphae. An important aspect of the life
sampled further north and east, they might have discovered the full extent
of individual 1s boundary. Although Anderson and colleagues discov-
ered several large A. gallica individuals, the largest was estimated to cover
15 hectares. All of the fungal samples collected from this area had the
same mating type, similar mitochondrial DNA restriction patterns, even
if individual haploid cultures were not exactly the same, and the same
11 RAPD fragments. Because of the variation among individual haploid
cultures, the researchers knew that each of these loci were heterozygous in
the diploid condition, allowing them to reject the hypothesis that these
samples were from different but closely related individuals.
Anderson and colleagues next set out to estimate the biomass and
age of the largest individual, individual 1. To estimate age, the scientists
had to estimate the rate of expansive growth outward from the center.
They assumed that the rate of growth was constant, which allowed them
to back-calculate to determine how long it took individual 1 to expand
to its current size. They used three methods to estimate the growth rate
(Table 1). Anderson and colleagues measured the maximum linear growth
of rhizomorphs along wooden stakes during one growing season. The sci-
entists also measured the maximum growth rate of cultures in the labora-
tory at different temperatures. To estimate mass, the scientists collected
soil samples, carefully separated fungal rhizomorphs from roots and soil,
dried the material, and weighed it to obtain the biomass per unit area of
soil. The wet mass was also estimated.
Anderson and colleagues knew that soil temperatures in the forest
ranged from 14o C to 16o C for about 90 days per year; and the rest of
the year, temperatures were below 14o C. They then calculated the an-
nual growth rate of laboratory cultures using the daily growth at 15o C
for 90 days, which is 0.189 m/year (2.1 mm/day * 90 days * 1 m/100 mm).
This is quite comparable to the annual growth on wooden stakes in the
forest soil (0.197 m/year). If this individual fungus grows in all direc-
tions at the same rate from a central point, it would be circular, and the
maximum distance across would be the diameter of the circle. The ra-
dius is half of that, which is the maximum distance it grew during its
life. If it grew steadily at 0.193 m/year (the average of the two estimates
made by the scientists), then this fungus is 1,645 years old [(635 m/2)/
(0.193 m/year)]! Anderson and colleagues argued that this may actually
be an underestimate of the age of the fungus, because competition with
other honey mushroom individuals would slow growth, as would adverse
climate conditions (such as, cold growing seasons).
The wet mass of the honey mushroom in the Michigan forest was
calculated based on the average wet mass estimate of 64.4 g/m2. First
convert the area to hectares, using the conversion of 10,000 m2/hectare.
Second, convert grams to kilograms by dividing by 1,000. Finally, multi-
ply by 15 hectares, which is the estimated area occupied by individual 1,
to obtain 9,660 kg. That is 9.66 metric tons, and when Anderson and
colleagues multiplied that by 10 to obtain the estimated total fungal mass,
they obtained 96.6 metric tons, which is close to the mass of an adult blue
whale! This may well alter perception of what an individual is. This one
individual fungus likely grew vegetatively for centuries to become a very
old and large individual.
Not all fungi grow to this size; in fact, most are much smaller and
often multiple individuals of the same species live in the same soil, un-
like the situation with the honey mushroom. But individuals of other
species of fungi have been shown to achieve sizes of the magnitude of the
honey mushroom individual, so it is not uncommon. A phenomenon
about fungal growth is that it is dynamican individual can lose mass
in one area and regrow it later. Fungal tissue is not as highly integrated as
the tissues of a blue whale. The property of the individual emerges from
the hyphae, mycelia, and rhizomorphs that make up the individual, and
in this instance that individual occupies space that no other honey mush-
room can occupy.
THE DEFINITION OF THE INDIVIDUAL CAN BE STRETCHED 7
150 workers were marked with colored paint that indicated the date and
transferred to experimental hives every other day until colonies contained
4,000 to 5,000 worker bees, which took about 4 weeks. Once a hive was
of a certain age, the queen began producing her own workers, and those
bees were unmarked.
The scientists manipulated temperature by placing hives in a stream
of air at one of five temperatures. The scientists measured air temperature
near bees using thermocouples in various places within the hive, includ-
ing near sealed brood cells (where larvae developed), open brood cells
(where larvae are fed by workers), empty cells, pollen cells (where pollen
is stored), and sealed or open honey cells (where honey is stored).
The scientists measured the head, thorax, and abdomen temperatures
of marked bees of varying ages in different positions in the hive (Figure 3).
The scientists recorded the bees position, its age, its temperature, and the
hive temperature where the bee was located (Figure 4).
The researchers calculated the percentage of bees of each age in
each location at each ambient temperature with thorax temperatures
36, 0C
36
34
32
30
28
26
24
23, 0C
= Tthorax
= Tcell rim
47
1183
= Ta
436
487
1410
836
234
496
540
370
1079
364
711
345
284
533
270
171
334
56
560
250
temperature (C)
450
63
60
404
387
37
174
74
74
42
27
17
Texp (C)
15
20
25
30
34
15
20
25
30
34
15
20
25
30
34
15
20
25
30
34
15
20
25
30
34
15
20
25
30
34
sealed brood open brood empty cells pollen open honey sealed honey
100 brood
25
0
15 20 25 30 34
A experimental temperature (C)
100 non-brood
percentage of worker bees
75
50
25
0
15 20 25 30 34
B experimental temperature (C)
taking turns with the task. Additionally, honey bees of different ages ap-
pear to be performing different tasks, which is something that individual
cells in a multicellular organism do.
Although a colony of bees is a collection of individuals, the entire
hive may act like an individual, which is called a superorganism by some
scientists. The hive is a property that emerges from a collection of honey
bees, each a part of the whole, and the properties of the hive are greater
than the sum of the parts. Honey bees produce metabolic heat to main-
tain the temperature of the hive within certain limits but only at or near
brood cells. This is analogous to the maintenance of constant body tem-
perature in an endothermic animal. Thermal homeostasis of a honey bee
colony is the result of the cooperation of thousands of individuals. Our
concept of the individual can be expanded to include biological entities
like a honey bee hive. The study presented here explores but one aspect of
honey bee hives as individuals. In fact, the hive is a highly integrated en-
tity, and bees exhibit communication to more efficiently forage for food,
defend the hive, and grow. The cells and tissues in an individual animal
also display these properties.
Multicellular organisms display division of labor. Within an indi-
vidual organism, a variety of cells perform different tasks, and all of the
cells are integrated into a whole organism. The individual is a property
that emerges from this collection of parts. An individual organism can be
more than that, and the boundary of an individual is not always clear. An
organism may only be part of a much larger whole with the parts com-
municating and cooperating to produce a biological entity that has more
flexible responses to varying environmental conditions than any single
part has.
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1992.
THE DEFINITION OF THE INDIVIDUAL CAN BE STRETCHED 15
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