Abstract
A NUMBER of population genetics models predict the evolution of male sexual ornaments through female choice1, but their genetic assumptions and predictions have hardly been investigated2,3. A key feature of these models is a positive genetic correlation between male ornaments and female preference for them4. Here I test this prediction at the within-population level with three-spined sticklebacks, Gasterosteus aculeatus, which show conspicuous sexual dichromatisnr. Intense red males are preferred in various situations6–10, but there is great intrapopulational variation in redness both among wild-caught6,10 and among laboratory-bred males11, which is partly environmental6 and may be partly genetic12,13. Also, females show considerable intrapopulational variation in their preference for redder males6,8,9, which is partly environmental8,9. Wild-caught, intense red males and dull males were crossed with a number of females from the same population in a full-sib/half-sib breeding design. Daughters were tested for their preference for more intensely red males, and the sons' coloration was quantified. Both traits showed genetic variation. Also the redness of the sons correlated with the preference for red of their sisters, thus the two traits show positive genetic correlation.
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References
Maynard Smith, J. Trends Ecol. Evol. 6, 146–151 (1991).
Heisler, L. et al. in Sexual Selection: Testing the Alternatives (eds Bradbury, J. W. & Andersson, M. B.) (Wiley, Chichester, 1987).
Bakker, T. C. M. Neth. J. Zool. 40, 617–642 (1990).
Kirkpatrick, M. & Ryan, M. J. Nature 350, 33–38 (1991).
Darwin, C. The Descent of Man, and Selection in Relation to Sex (Murray, London, 1871).
Milinski, M. & Bakker, T. C. M. Nature 344, 330–333 (1990).
McLennan, D. A. & McPhail, J. D. Can. J. Zool. 68, 482–492 (1990).
Bakker, T. C. M. & Milinski, M. Behav. Ecol. Sociobiol. 29, 205–210 (1991).
Milinski, M. & Bakker, T. C. M. Proc. R. Soc. B250, 229–233 (1992).
Bakker, T. C. M. & Mundwiler, B. Behav. Ecol. (in the press).
Bakker, T. C. M. Behaviour 98, 1–144 (1986).
Hagen, D. W. & Moodie, G. E. E. Evolution 33, 641–648 (1979).
Bakker, T. C. M. in The Evolutionary Biology of the Threespine Stickleback (eds Bell, M. A. & Foster, S. A.) (Oxford Univ. Press. Oxford, in the press).
Laurent, P. J. J. Fish. Res. Bd. Canada 29, 867–875 (1972).
Falconer, D. S. Introduction to Quantitative Genetics 3rd edn (Longman, Harlow, 1989).
Frischknecht, M. Evol. Ecol. (in the press).
Becker, W. A. Manual of Quantitative Genetics 4th edn (Academic Enterprises, Pullman, 1985).
Robertson, A. Biometrics 15, 469–485 (1959).
Lande, M. Proc. natn. Acad. Sci. 78, 3721–3725 (1981).
van Noordwijk, A. J. in Population Biology and Evolution (eds Wöhrman, K. & Loeschcke, V.) (Springer, Heidelberg, 1984).
Kearns, P. W. E., Tomlinson, I. P. M., Veltman, C. J. & O'Donald, P. Heredity 68, 385–389 (1992).
O'Donald, P. & Majerus, M. E. N. Heredity 69, 521–526 (1992).
Ritchie, M. G. Trends Ecol. Evol. 7, 328–329 (1992).
Kirkpatrick, M. Evolution 36, 1–12 (1982).
Seger, J. Evolution 39, 1185–1193 (1985).
Heisler, I. L. Heredity 55, 187–198 (1985).
Kirkpatrick, M., Price, T. & Arnold, S. J. Evolution 44, 180–193 (1990).
Barton, N. H. & Turelli, M. Genetics 127, 229–255 (1991).
Pomiankowski, A., Iwasa, Y. & Nee, S. Evolution 45, 1422–1430 (1991).
Iwasa, Y., Pomiankowski, A. & Nee, S. Evolution 45, 1431–1442 (1991).
Kirkpatrick, M. J. theor. Biol. 119, 263–271 (1986).
Tomlinson, I. P. M. Heredity 60, 283–293 (1988).
Sokal, R. R. & Rohlf, F. J. Biometry 2nd edn (Freeman, New York, 1981).
Endler, J. A. Biol. J. Linn. Soc. 41, 315–352 (1990).
Endler, J. A. Vision Res. 31, 587–608 (1991).
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Bakker, T. Positive genetic correlation between female preference and preferred male ornament in sticklebacks. Nature 363, 255–257 (1993). https://doi.org/10.1038/363255a0
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DOI: https://doi.org/10.1038/363255a0
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