1217 Refinement of Methods for Sexing Instars and Caste Members in Neotermes koshunensis (Isoptera, Kalotermitidae) by Yasushi Miyaguni 1,2, Koji Sugio 3, Kazuki Tsuji 4 ABSTRACT Exact sexing of individuals is important to an understanding of termite societies. We found that the female-specific sexual character of the elongated seventh sternite, known in other termites, is useful for distinguishing the sex of individuals of the dry-wood termite Neotermes koshunensis (Shiraki) from the fifth instar onward. The method described is highly efficient at sexing instars, nymphs, soldiers and alates. Keywords: Dry-wood termites, Kalotermitidae, Neotermes koshunensis, morpholog y, sexual dimorphism. INTRODUCTION Insect societies among the Hymenoptera and Isoptera (termites) di- vide labor between reproductive and non-reproductive castes, whereas in hymenopteran societies males almost never play any social role. In termite societies males and females are assumed to share the same social roles (Krishna 1969, Holldöbler & Wilson 1990, Roisin 2000). However, a growing body of empirical evidence suggests that this premise in termites does not always hold true, and caste-specific sex biases have been reported (Roisin 2000). For a better understanding of the roles of the sexes in termite social systems, we need more empirical data on various termite taxa. With this aim, the sexing of individual termites is indispensable. However, the small morphological differences between male and female termites often make morphological sexing difficult. \1Environmental Science and Conservation Biolog y, United Graduate School of Agricultural Sciences, Kagoshima University, Kagoshima 890-8580, Japan 2Corresponding author: E-mail: neotenic_of_termite@yahoo.co.jp 3Department of Science Education, Faculty of Education, University of the Ryukyus, Okinawa 903- 0213, Japan 4Entomological Laboratory, Faculty of Agriculture, University of the Ryukyus, Okinawa 903-0213, Japan 1218 Sociobiolog y Vol. 59, No. 4, 2012 Alates (imagos) of many termites show a female-specific morphological character, viz., a widely extended seventh sternite that covers most or all of the eighth and ninth sternites (Weesner 1969). In some species, immature females also show similar sexual characteristics that can be used for sexing (Thompson & Synder 1920, Mensa-Bonsu 1976, Myles & Chang 1984, Roisin 1992). Zimet and Stuart (1982) described the sexual dimorphism in immature stages of Reticulitermes flavipes (Rhinotermitidae), providing currently the most useful information for sexing immature stages of termites. However, they did not identify the stage at which this character becomes practical for sexing. So far no study has examined the validity of this sexing method in every developmental stage of immatures. We did so by observation of the sternite structure in all immature stages of Neotermes koshunensis (Kalotermitidae), followed by confirmation of sex by gonadal dissection. MATERIALS AND METHODS N. koshunensis is distributed from Taiwan to Okinawa (Ikehara 1966). A colony of N. koshunensis collected on the main island of Okinawa in September 2009 was reared in the laboratory (in the dark at ambient temperature) using a plastic box with pine woods as food for about 2 months before the study. A preliminary examination showed that alates of this species show sexual di- morphism in the sternites (Y. Miyaguni, unpublished data). For every instar, nymphal stage and alates, we used the morpholog y of the sternites to classify individuals into putative females and putative males under a stereomicroscope (×40 magnification at maximum). We then dissected 30 putative females and 30 putative males of each instar and caste to determine the true sex through inspection of the gonads (Thompson and Synder 1920). Instars and castes were defined according to Katoh et al. (2007). The sternite structures were recorded on a digital camera attached to the stereomicroscope (Olympus E-System E-330; Olympus Corporation, Tokyo, Japan). RESULTS The sexual dimorphism of nymphs was very clear, especially in pre-alates, which could be sexed under a magnifying glass (×10). Sixth instar females showed considerable individual variation in the degree of sternite develop- ment, ranging from only a slight extension to near complete coverage of the 1219 Miyaguni, Y. et al. — Methods for Sexing in Neotermes koshuensis eighth sternite (Fig. 1). The sexual difference in soldiers was similar to that of sixth instars. It was less conspicuous in fifth instars (Figs. 1, 2). Despite this variation, dissections revealed that our sexing of individuals using this morphological indicator was 100% accurate in those developmental stages and castes (Table 1). Some fourth instar females did not show a sexual character and were misclassified as males, although we correctly determined the sex of other females (Table 1). There was a significant difference in the proportion of misidentified individuals between fifth and fourth instars (Fisher’s exact test, P < 0.001). All third instars were classified as males by our criterion, as this instar showed no sexual difference in the sternite configuration (Table 1). In first and second instars, the gonads were indistinguishable between Fig. 1. The illustration of the sternite structures of females in N. koshunensis. Numerals on illustration show the sternite numbers. 3L - 6L, third to sixth instar; pre-A, pre-alate nymph; A, alate. 1220 Sociobiolog y Vol. 59, No. 4, 2012 testes and ovaries, and therefore it was not possible to determine the sex. Thus, sexing using the seventh sternite was highly accurate in all stages from the fifth instar onward. DISCUSSION The sexual characteristics of N. koshunensis females begin to develop from the fourth instar, but the sexual difference in the sternites from the fifth in- star on becomes conspicuous enough to be informative as a morphological indicator of sex (Table 1, Figs. 1, 2). In termite species that have a linear caste developmental pathway, the timing or stage at which the wing buds begin to develop differs among individuals (Roisin 2000, Katoh et al 2007). The varia- tion that we found in the seventh sternite morpholog y in the fourth to sixth Table 1. The result of sexing based on sexual dimorphism. Instars & castes n True sex Proportion misidentified Male Female Putative male 3rd instar 30 20 10 0.3 4th instar 30 18 12 0.4 5th instar 30 30 0 0.0 6th instar 30 30 0 0.0 Early nymph 30 30 0 0.0 Pre-alate nymph 30 30 0 0.0 Alate 30 30 0 0.0 Soldier 30 30 0 0.0 Putative female 3rd instar - - - - 4th instar 30 0 30 0.0 5th instar 30 0 30 0.0 6th instar 30 0 30 0.0 Early nymph 30 0 30 0.0 Pre-alate nymph 30 0 30 0.0 Alate 30 0 30 0.0 Soldier 30 0 30 0.0 1221 Miyaguni, Y. et al. — Methods for Sexing in Neotermes koshuensis instar females of N. koshunensis may reflect a similar individual difference in development. Although the generality of our finding in N. koshunensis is still to be confirmed in other colonies, our study indicates that sternite morphol- og y can be used for sexing some younger stages. ACKNOWLEDGMENTS We thank H. Tatsuta, E. Vargo, H. Tanaka, S. Dobata and M. K. Hojo. who kindly gave us invaluable advice during the course of the study. Fig. 2. The illustration of the sternite structures of males in N. koshunensis. Numerals on illustration show the sternite numbers. 3L - 6L, third to sixth instar; pre-A, pre-alate nymph; A, alate. 1222 Sociobiolog y Vol. 59, No. 4, 2012 REFERENCES Hölldobler, B. & E. O. Wilson 1990. The Ants. Cambridge, MA. Harvard Univ. Press. 732 p. Ikehara, S. 1966. Distribution of termites in Ryukyu Archipelago. Bulletin of Arts & Science Division, University of the Ryukyus, (Mathematics & Natural Sciences). 9: 49-178. Katoh, H., T. Matsumoto & T. Miura 2007. Alate differentiation and compound-eye development in the dry-wood termite Neotermes koshunensis (Isoptera, Kalotermitidae). Insectes Sociaux 54: 11-19. Krishna, K. 1969. Introduction. pp. 1-18. In: Krishna, K. & F. M. Weesner (eds.). Biolog y of Termites Vol.1. Academic Press. New York. Mensa-Bonsu, A. 1976. The production and elimination of supplementary reproductives in Porotermes adamsoni (Froggatt) (Isoptera, Hodotermitidae). Insectes Sociaux 23: 113-154. Myles, T. G. & F. Chang 1984. The caste system and caste mechanisms of Neotermes connexus (Isoptera: Kalotermitidae). Sociobiolog y 9 (3): 163-319. Roisin, Y. 1992. Development of non-reproductive castes in the neotropical termite genera Cornitermes, Embiratermes and Rhynchotermes (Isoptera, Nasutitermitinae). Insectes Sociaux 39: 313-324. Roisin Y. 2000. Diversity and Evolution of Caste Patterns. pp. 95-119. In: T. Abe, D. E. Bignell & M. Higashi (eds.). Termites: Evolution, Sociality, Symbioses, Ecolog y. Kluwer Academic Publishers. Dordrecht. Thompson, C. B. & T. E. Synder 1920. The “third form,” the wingless reproductive type of termites: Reticulitermes and Prorhinotermes. Journal of Morpholog y. 34 (3): 591- 633. Weesner, F. M., 1969. External Anotomy pp. 19-47. In: Krishna, K. & F. M. Weesner (eds.). Biolog y of Termites Vol.1. Academic Press. New York. Zimet, M. & A. M. Stuart 1982. Sexual dimorphism in the immature stages of the termite, Reticulitermes flavipes (Isoptera: Rhinotermitidae). Sociobiolog y 7 (1): 1-7