Some evidence for different ecological pressures that constrain male and female body size
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The dwarf morph of the Lake Tanganyika cichlid Telmatochromis temporalis uses empty snail shells as shelters and breeding sites in shell beds, in which many empty shells exist. Here, we assessed selection forces regulating body size in this fish. Field observations showed that large males tended to have a greater number of females in their territories, suggesting that sexual selection favours large males. Nonetheless, a transplant experiment suggested that male body size was limited by the ability to hide in empty shells from large piscivorous fish. In females, the number of ovarian eggs increased with body size, suggesting that fecundity selection favours large females. However, females are smaller than males. Females spawned eggs close to the apices inside the shells. The small space there would decrease the risk of egg predation by egg predators, and small body size of females may be a result of adaptation to spawn eggs in the small, safe spaces. This study provides support for the idea that male and female body sizes have been limited by different ecological pressures (predation on adult fish in males, predation on eggs in females), which has not been reported previously in any animal.
KeywordsTelmatochromis temporalis Lake Tanganyika Sexual selection Fecundity selection Natural selection
We thank H. Phiri, D. Sinynza, and the other staff of the Lake Tanganyika Research Unit in Mpulungu for support in the field; T. Komai for identifying crab species; E. Nakajima and D. Sinynza for providing language help; T. Sota, Y. Takami and H. Toju for advice on research. This study was supported by Grants-in-Aid for JSPS Fellows (No. 20188), for Special Purposes (No. 18779002), for Young Scientists (No. 20770065), and Scientific Research (No. 23370043) to TT, Grant-in-Aid for Scientific Research (No. 22405010) to MK, and Global COE Program (A06) to Kyoto University.
- Erlinge, S., 1987. Why do European stoats Mustela erminae not follow Bergmann’s rule? Holarctic Ecology 10: 33–39.Google Scholar
- Hori, M., 1997. Structure of littoral fish communities organized by their feeding activities. In Kawanabe, H., M. Hori & M. Nagoshi (eds), Fish Communities in Lake Tanganyika. Kyoto University Press, Kyoto: 275–298.Google Scholar
- Poll, M., 1956. Poissons Cichlidae. Résultats scientifiques. Exploration hydrobiologique du Lac Tanganika (1946–1947). Institut Royal des Sciences Naturelles de Belgique 3(5B): 1–619.Google Scholar
- Sato, T. & M. M. Gashagaza, 1997. Shell-broong cichlid fishes of Lake Tanganyika: their habitats and mating systems. In Kawanabe, H., M. Hori & M. Nagoshi (eds), Fish Communities in Lake Tanganyika. Kyoto University Press, Kyoto: 219–240.Google Scholar
- Schluter, D., 2000. The Ecology of Adaptive Radiation. Oxford University Press, Oxford.Google Scholar
- Schütz, D. & M. Taborsky, 2000. Giant males or dwarf females: what determines the extreme sexual size dimorphism in Lamprologus callipterus? Journal of Fish Biology 57: 1254–1265.Google Scholar
- Schütz, D., G. A. Parker, M. Taborsky & T. Sato, 2006. An optimality approach to male and female body sizes in an extremely size-dimorphic cichlid fish. Evolutionary Ecology Research 8: 1–16.Google Scholar
- Sokal, R. R. & F. J. Rohlf, 1995. Biometry, 3rd ed. Freeman, New York.Google Scholar
- Stearns, S. C., 1992. The Evolution of Life Histories. Oxford University Press, Oxford.Google Scholar
- Tracy, C. R., 1999. Differences in body size among chuckwalla (Sauromalus obesus) populations. Ecology 80: 259–271.Google Scholar
- Uhl, G., S. Schmitt, M. A. Schaefer & W. Blanckenhorn, 2004. Food and sex-specific growth strategies in a spider. Evolutionary Ecology Research 6: 523–540.Google Scholar