Current Biology 24, 10061010, May 5, 2014 2014 Elsevier Ltd All rights reserved

http://dx.doi.org/10.1016/j.cub.2014.03.022

Report
Female Penis, Male Vagina, and Their
Correlated Evolution in a Cave Insect
Kazunori Yoshizawa,1,* Rodrigo L. Ferreira,2
Yoshitaka Kamimura,3 and Charles Lienhard4
1Systematic Entomology, School of Agriculture, Hokkaido
University, Sapporo 060-8589, Japan
2Biology Department, Federal University of Lavras,
37200-000 Lavras, MG, Brazil
3Department of Biology, Keio University, Yokohama 223-8521,
Japan
4Natural History Museum of the City of Geneva, CP 6434,
1211 Geneva 6, Switzerland

Summary
Sex-specific elaborations are common in animals and have
attracted the attention of many biologists, including Darwin
[1]. It is accepted that sexual selection promotes the evolution of sex-specific elaborations. Due to the faster replenishment rate of gametes, males generally have higher potential
reproductive and optimal mating rates than females. Therefore, sexual selection acts strongly on males [2], leading to
the rapid evolution and diversification of male genitalia [3].
Male genitalia are sometimes used as devices for coercive
holding of females as a result of sexual conflict over mating
[4, 5]. In contrast, female genitalia are usually simple. Here
we report the reversal of intromittent organs in the insect
genus Neotrogla (Psocodea: Prionoglarididae) from Brazilian caves. Females have a highly elaborate, penis-like structure, the gynosome, while males lack an intromittent organ.
The gynosome has species-specific elaborations, such
as numerous spines that fit species-specific pouches in
the simple male genital chamber. During prolonged copulation (w4070 hr), a large and potentially nutritious ejaculate
is transferred from the male via the gynosome. The correlated genital evolution in Neotrogla is probably driven by
reversed sexual selection with females competing for seminal gifts. Nothing similar is known among sex-role reversed
animals.
Results and Discussion
The genus Neotrogla (Figure 1A) contains four named species
(adult body length 2.73.7 mm) [6, 7]. Its most striking feature is
the presence of a large penis-like structure in the female,
termed a gynosome (Figures 1, 2, and 3; Figures S1, S2, and
S3 available online). We show here that the gynosome is erectile, basally membranous, and apically sclerotized. Its sclerotized part consists of a proximal rod-like extension and a
penis-like distal prominence. The latter encloses a duct leading to the sperm storage organ (spermatheca), and is interpreted as a novel structure differentiated from the opening
region of the spermathecal duct (Figure 1, light blue) [6]. In
contrast, the male genitalia (phallosome) consist of a simple,
thin arc lacking an intromittent organ (Figures 1G and 3E). In
related insects, the spermathecal duct has a simple opening
and the phallosome is well developed (Figure 1).

*Correspondence: [email protected]

We observed coupling in all Neotrogla species and found that

the gynosome acts as an intromittent organ to receive voluminous spermatophores from the male. As in most related taxa,
including those having well-developed male genitalia (Figure 1C) [8], the male is positioned under the female during copulation (Figure 1A). The apical sclerotized part of the gynosome,
bearing the opening of the spermathecal duct, deeply penetrates the male (Figures 2, 3, S2, and S3), and its tip fits the opening of the seminal duct (Figures 2D and 3C). The membranous
part inflates within the male genital chamber, and numerous
spines on the membrane internally anchor the female to the
male (Figures 2B, 2E, 3A, 3D, and S2). In this position, the
male sternum is gripped between the female paraprocts and
inflated gynosome (Figures 2B and 2C). Only the connection
of the abdominal tips holds pairs fixed in copula together.
Furthermore, pulling apart coupled specimens (N. curvata:
n = 1) led to separation of the male abdomen from the thorax
without breaking the genital coupling, showing that the female
can hold the male tightly using the gynosome and paraprocts.
The gynosomal structures are species specific. The distal
sclerotized part is strongly curved in N. curvata (Figures 2A
2D), but is straight or only slightly curved in other species (Figures 3 and S2). The membranous region of N. curvata has a
smooth dorsal lobe (yellow) and five areas bearing sclerotized
spines: a dorsal (red), a pair of lateral (green), and a pair of
ventrolateral (purple) spiny areas (Figure 2). In N. aurora and
N. brasiliensis, the dorsal and lateral spiny areas are present
(Figure S2), but the dorsal lobe and ventrolateral spiny areas
are absent. The gynosome of N. truncata lacks all elaborations, but its membranous part is densely covered by tiny bristled spines (Figure 3).
Male genitalia are simple, but also species specific, corresponding to the gynosomal structures (Table S1). In
N. curvata, the seminal duct is strongly curved, as is the gynosomal apical sclerite (Figures 2B2D), whereas these are
straight or only slightly curved in the others (Figure 3 and
S2). The male genital chamber of N. aurora, N. brasiliensis,
and N. curvata has lateral pouches corresponding to the lateral
spiny areas of the gynosome (Figures 1G, 2, S1B, and S2,
green arrowheads), while ventrolateral spiny areas and corresponding male pouches are only present in N. curvata (Figures
2B, 2E, and S1B, purple arrowheads). During copulation, the
spiny areas fit into the corresponding pouches and anchor
the female (Figures 2 and S2). The gynosome of N. truncata
lacks strong spines (Figure 3A and 3D), and the female of
this species anchors itself using the entire surface of the bristled gynosomal membrane (Figure 3A and 3D). The male genital chamber of this species lacks any pouches (Figure 3E,
open green arrowheads).
Spiny genitalia are present in many male animals [3, 5, 9].
These may be used as stimulatory devices [10, 11] or may
result from sexual conflict [12, 13], in addition to having an
anchoring function to grasp and hold mates. Species-specific
membranous pouches in female genitalia are reported in
some insects to accommodate the male genitalia [5, 9] and
thereby reduce the cost of mating imposed by the corresponding male genital spines. The relative function and pattern
of elaboration of male and female genitalia in Neotrogla are
completely reversed relative to that generally observed.

Reversed Intromittent Organs

1007

Figure 1. Male and Female Genitalia of Prionoglarididae

(A) Neotrogla curvata in copula.
(B and C) Prionoglaris dactyloides spermathecal
duct opening (B; light blue) and phallosome (C).
(D and E) Speleketor irwini, same as in (B) and (C).
(F and G) Neotrogla aurora gynosome (F; parts
highlighted as in Figures 2 and 3) and phallosome
(G). The green arrowhead in (G) indicates the left
lateral pouch in the male genital chamber.
Scale bars represent 0.1 mm. See also Figure S1
and Table S2.

In certain astigmatan mites [14] and scirtid beetles [15],

male genitalia are reduced and females possess an elongated intromittent tube or an eversible genital duct, respectively. Although these organs are used to obtain sperm
or spermatophores, no anchoring mechanism has been
observed. Female seahorses have an intromittent ovipositor
to deposit eggs in the male brood pouch [16], but this is
not a penis. The evolution of a female penis is likely to be
strongly constrained because, in internally fertilizing animals,
the ancestral condition is exclusively that of an inseminating
male requiring an intromittent organ and a receiving female,
so that integrated modifications in male and female structures and behaviors are required [17]. Therefore very few animals have reversed intromittent copulatory organs.
It is known that reversed sexual selection has sometimes
caused the evolution of masculine characteristics or of
secondary genitalia in females. For example, female ground
weta (Orthoptera: Anostostomatidae: Hemiandrus pallitarsis)
benefit from seminal gifts and compete intensely for them
[18], using an elbow-shaped structure located in the middle
of the abdomen to obtain them from males. An anchoring intromittent organ, such as the gynosome, might be even more
effective at taking up seminal gifts from males. Nevertheless,
reversed intromittent organs were previously unknown among
animals with reversed sexual selection.
Insects related to Neotrogla suggest the potential of nuptial
gifts favoring the evolution and diversification of the gynosome. In Lepinotus patruelis (Trogiidae), the direction of sexual

selection is reversed (without reversal of

the intromittent organ). Males of this
species transmit specialized spermatophores (seminal capsules formed during
copulation within the females spermatheca), which are produced by the
enlarged seminal duct [19]. Males are
choosier about mates than females,
indicating the costs of spermatophore
production, while females compete for
the nutritious seminal gift [19, 20]. In
Neotrogla, similarly shaped spermatophores (Figures 3F, S3C, and S3D) and
an enlarged seminal duct producing
voluminous spermatophore material
(Figures 2B, S3A, and S3B) are present,
suggesting that Neotrogla males also
donate a nutritious seminal gift to
females. All known Neotrogla species inhabit extremely dry oligotrophic
caves and feed on bat guano and bat
carcasses, which are relatively scarce
resources [6, 7]. Under such circumstances, nutritious seminal
gifts cause a strong selection pressure for increased female
mating rate [21]. During their life, Neotrogla females may acquire several spermatophores (up to 11 have been observed
in N. brasiliensis) (Figures 3F and S3C) [6]; they are evidently
polyandrous. We also observed that females consumed the
contents of the spermatophores after their first mating before
producing mature eggs (n = 5; Figure S3D), suggesting that
the contents of the spermatophores are probably used for
nutrition as well as fertilization.
This interpretation may explain the following unique characteristics of the female internal genitalia and of the coupling
behavior of Neotrogla. The spermathecal duct of Neotrogla
is divided by a spermathecal plate, such that the female can
simultaneously maintain two filled spermatophores (Figures
3F and S3C), something unknown in related taxa [19, 22].
The duration of copulation in N. curvata is exceptionally long
(52.5 6 11.2 hr, mean 6 SD, range 4173 hr, n = 12; Table
S2) in comparison with related taxa: approximately 40 min
in Prionoglaris stygia [8], approximately 2 hr in Trogium pulsatorium [22], and a maximum of 4 hr in the genus Lepinotus [8,
19]. In Neotrogla, females have structures that can coercively
hold males. The very long copulation, as well as polyandry,
is probably controlled by females to obtain more seminal gifts
from males.
Sexual conflict over the donation of a nutritious seminal
gift is thus the most likely factor favoring the evolution of
the gynosome. This organ may have a premating function

Current Biology Vol 24 No 9

1008

Figure 2. Terminal Structures of Neotrogla curvata

The following parts of the gynosome are highlighted: distal sclerite (light blue); basal rod (orange); and membranous region with dorsal lobe (yellow) and
lateral (green), dorsal (red), and ventrolateral (purple) spiny areas. The corresponding male genital pouches are indicated by arrowheads of the same color.
(A) Erect gynosome, dorsolateral view.
(BE) Terminal abdomens in copula, lateral (BD), and ventral (E) views. The gynosome tip and seminal duct opening are magnified in (D). In the schematic
drawing (C), female structures, except for the distal part of the gynosome, are indicated in orange and male structures in gray.
Scale bars represent 0.1 mm. See also Figure S2 and Table S1.

grasping reluctant mates or a postmating function holding

mates to ensure prolonged copulation, although these functions are not mutually exclusive. Because other paternal
investments, such as parental care, are not observed in Neotrogla, the correlated evolution of morphologically and functionally novel genital organs has probably been driven by
reversed sexual selection on copulatory function. Sex-rolereversed animals are valuable for testing the generality of
theories of sexual selection [23]. Because sex-role-reversed
females usually cannot coercively hold males, they may be
constrained in terms of evolving adaptations that relate to
sexual conflict. The female genital anchoring mechanism
of Neotrogla, correlating morphologically with specialized
reduced male genitalia, is unique, and nothing similar is
known among other sex-role-reversed animals. However, in
addition to anchoring, the gynosomal spines may have other
functions, such as genital stimulation or inflicting harm. The
evidence for reversed sexual selection and sexual conflict
provided here is mostly circumstantial, but further controlled
studies of the mating system of Neotrogla species, together
with an exploration of their phylogeny, would provide an
extremely rare opportunity to test the generality and relative
importance of some hypotheses about sexual selection

[15, 913]. Neotrogla also offers a significant opportunity

to study evolutionary novelty, an area of central interest in
contemporary evolutionary biology [17, 24].
Experimental Procedures
See the Supplemental Information for additional details.
Sampling
Neotrogla specimens in copula were killed with hot water (w80 C) and fixed
with 80% ethanol in caves. We observed three pairs of N. aurora, four pairs
of N. brasiliensis, 11 pairs of N. curvata, and six pairs of N. truncata.
Morphological Observations
We used BABB (1:2 benzyl alcohol:benzyl benzoate) to make muscles and
sclerites transparent for examination [25]. This method does not dissolve
soft tissues, and specimens in copula can be observed in situ (Figures 2D
and 3C). However, BABB could not make fat bodies transparent, and we
used 1% KOH to dissolve soft internal tissues after embedding abdomens
in 1% agarose. Observations were performed in glycerol (unmounted)
or after slide mounting (dissected female and male genitalia). An Olympus
SZX16 stereo microscope and a Zeiss Axiophot compound light microscope were used for examination. Photographs were taken with an Olympus
E-330 or OM-D E-M5 digital camera attached to the microscopes. Partially
focused photographs were combined using Helicon Focus (Helicon Soft) to
obtain images with high field depth.

Reversed Intromittent Organs

1009

Figure 3. Terminal Structures of Neotrogla

truncata
Color scheme as in Figure 2, plus pink color indicating the basal gynosomal membrane.
(AD) Terminal abdomens in copula, lateral (AC)
and ventral (D) views. (B) shows a schematic
drawing. The gynosome tip and seminal duct
opening are magnified in (C).
(E) Slide-mounted male genitalia. Green open
arrowheads indicate a lack of membranous
pouches. See Figure 1G for comparison.
(F) Spermatheca fixed during copulation. Seven
spermatophores are present, of which two
attached to the spermathecal plate are filled
(indicated by white asterisks); the others are
separated from the plate and are empty (black
asterisks).
Scale bars represent 0.1 mm. See also Figure S3
and Table S1.

Behavioral Observations
A total of 12 couplings of N. curvata were observed (Table S2). Specimens
were kept in Styrofoam boxes during observation. Adults were placed
together, and when a couple formed, it was placed in a separate vial for
observation. Copulations were observed at 30 min intervals. After copulation, some pairs were kept for observation until they died (n = 2), sometimes
in the presence of their F1 nymphs.

concerning the cave locations, M. Villela, M. Michele Perdigao, and L. Faria

Ferreira for help with some mating observations, and J. Hollier for discussion and final language editing. This study was supported in part by CNPq
grant 301061/2011-4 to R.L.F., JSPS grant 22770058 to Y.K., and JSPS grant
24570093 to K.Y.

Supplemental Information

Received: January 7, 2014

Revised: February 12, 2014
Accepted: March 10, 2014
Published: April 17, 2014

Supplemental Information includes three figures, two tables, and Supplemental Experimental Procedures and can be found with this article online
at http://dx.doi.org/10.1016/j.cub.2014.03.022.

References

Acknowledgments
We thank F. Pellegatti-Franco for specimens, M. Souza Silva and
M. Medeiros for support in the field, E. Magalhaes for information

1. Darwin, C.R. (1871). The Descent of Man and Selection in Relation to

Sex (London: John Murray).
2. Trivers, R.L. (1972). Parental investment and sexual selection. In Sexual
Selection and the Descent of Man, 18711971, B.G. Campbell, ed.
(Chicago: Aldine Publishing Co), pp. 136179.

Current Biology Vol 24 No 9

1010

3. Eberhard, W.G. (1985). Sexual Selection and Animal Genitalia

(Cambridge: Harvard University Press).
4. Arnqvist, G., and Rowe, L. (2002). Correlated evolution of male and
female morphologles in water striders. Evolution 56, 936947.
5. Lange, R., Reinhardt, K., Michiels, N.K., and Anthes, N. (2013).
Functions, diversity, and evolution of traumatic mating. Biol. Rev.
Camb. Philos. Soc. 88, 585601.
6. Lienhard, C., Do Carmo, T.O., and Ferreira, R.L. (2010). A new
genus of Sensitibillini from Brazilian caves (Psocodea: Psocoptera:
Prionoglarididae). Rev. Suisse Zool. 117, 611635.
7. Lienhard, C., and Ferreira, R.L. (2013). A new species of Neotrogla from
Brazilian caves (Psocodea: Psocoptera: Prionoglarididae). Rev. Suisse
Zool. 120, 312.
8. Lienhard, C. (1998). Psocopte`res euro-mediterraneens. Faune France
83, ixx, 1517.
9. Kamimura, Y. (2012). Correlated evolutionary changes in Drosophila
female genitalia reduce the possible infection risk caused by male
copulatory wounding. Behav. Ecol. Sociobiol. 66, 11071114.
10. Bonduriansky, R. (2001). The evolution of male mate choice in insects:
a synthesis of ideas and evidence. Biol. Rev. Camb. Philos. Soc. 76,
305339.
11. Eberhard, W.G. (2010). Rapid divergent evolution of genitalia. In The
Evolution of Primary Sexual Characters in Animals, J.L. Leonard and
A. Cordoba-Aguilar, eds. (Oxford: Oxford University Press), pp. 4078.
12. Chapman, T., Arnqvist, G., Bangham, J., and Rowe, L. (2003). Sexual
conflict. Trends Ecol. Evol. 18, 4147.
13. Hotzy, C., Polak, M., Ronn, J.L., and Arnqvist, G. (2012). Phenotypic
engineering unveils the function of genital morphology. Curr. Biol. 22,
22582261.
14. Klimov, P.B., and Sidorchuk, E.A. (2011). An enigmatic lineage of mites
from Baltic amber shows a unique, possibly female-controlled, mating.
Biol. J. Linn. Soc. Lond. 102, 661668.
15. Nyholm, T. (1969). Uber Bau und Funktion der Kopulationsorgane bei
den Cyphones (Col. Helodidae). Studien uber die Familie Helodidae X.
Entomol. Tidskr. 90, 233271.
16. Williams, W.G. (1975). Sex and Evolution (Princeton: Princeton
University Press).
17. Muller, G.B., and Wagner, G.P. (2003). Innovation. In Keywords and
Concepts in Evolutionary Developmental Biology, B.K. Hall and W.M.
Olson, eds. (Cambridge: Harvard University Press), pp. 218227.
18. Gwynne, D.T. (2005). The secondary copulatory organ in female ground
weta (Hemiandrus pallitarsis, Orthoptera: Anostostomatidae): a sexually selected device in females? Biol. J. Linn. Soc. Lond. 85, 463469.
19. Wearing-Wilde, J. (1995). The sclerotized spermatophore of the barklouse Lepinotus patruelis. Tissue Cell 27, 447456.
20. Wearing-Wilde, J. (1996). Mate choice and competition in the barklouse
Lepinotus patruelis (Psocoptera: Trogiidae): The effect of diet quality
and sex ratio. J. Insect Behav. 9, 599612.
21. Gwynne, D.T. (2008). Sexual conflict over nuptial gifts in insects. Annu.
Rev. Entomol. 53, 83101.
22. Klier, E. (1956). Zur Konstruktionsmorphologie des mannlichen
Geschlechtsapparates der Psocopteren. Zool. Jb. (Anat.) 75, 207286.
23. Andersson, M. (1994). Sexual Selection (Princeton: Princeton University
Press).
24. Moczek, A.P. (2008). On the origins of novelty in development and evolution. Bioessays 30, 432447.
25. Kamimura, Y., and Mitsumoto, H. (2011). Comparative copulation
anatomy of the Drosophila melanogaster species complex (Diptera:
Drosophilidae). Entomol. Sci. 14, 399410.