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| subject: | Article] Sexual selection |
Sexual selection and genital evolution David J. Hosken and Paula Stockley Genitalia are conspicuously variable, even in closely related taxa that are otherwise morphologically very similar. Explaining genital diversity is a longstanding problem that is attracting renewed interest from evolutionary biologists. New studies provide ever more compelling evidence that sexual selection is important in driving genital divergence. Importantly, several studies now link variation in genital morphology directly to male fertilization success, and modern comparative techniques have confirmed predicted associations between genital complexity and mating patterns across species. There is also evidence that male and female genitalia can coevolve antagonistically. Determining mechanisms of genital evolution is an important challenge if we are to resolve current debate concerning the relative significance of mate choice benefits and sexual conflict in sexual selection. Extreme variation in male genital morphology is a conspicuous and comprehensive trend across animals with internal fertilization to the extent that even closely related species with similar general morphology often have strikingly different genitalia ( Figure 1). Explaining genital diversity has been a longstanding problem for evolutionary biologists, and the selective pressure(s) responsible for this bewildering array has been the subject of ongoing debate [1-3] . Complicated and divergent morphology is unlikely to have arisen purely for the relatively simple function of sperm transfer. So why the enormous variation ( Box 1)? Before the recent expansion of studies investigating the role of sexual selection in genital evolution, two general non-sexual selection explanations had been proposed ( Box 2), neither of which are currently well supported (reviewed in [1,2,4] ). By contrast, evidence is accumulating for a role of sexual selection in genital evolution. The idea that sexual selection influences genital evolution has been extensively developed by Eberhard in the context of postcopulatory sexual selection [1,4-6] . In particular, he has argued that genital divergence is often driven by cryptic female choice, broadly defined as any postcoupling process or structure controlled by females that biases paternity towards males having a certain phenotype when females have mated with more than one male [7]. Eberhard further argues that the female benefit for this choice is most often Fisherian ( Box 3). This has generated debate, however, because it can be difficult to distinguish mechanisms of cryptic female choice for sexy sons from good genes, or from other potential selection pressures involved in postcopulatory sexual selection, such as sperm competition and sexual conflict. The evolutionary effects of purely Fisherian benefits are also unclear ( Box 3). Moreover, sperm competition probably played at least some role in the initial evolution of male genitalia from a primordial state where gametes were released into the environment [8]. Hence, although a new generation of studies is consistent in supporting Eberhard's hypothesis that sexual selection is the primary force driving genital divergence, the exact selection mechanisms involved are less clear. Here, we discuss recent advances in our understanding of genital evolution, and the challenge of determining the relative importance of various mechanisms of sexual selection in the evolution of genital diversity. Read the rest at Nature http://gateways.bmn.com/magazine/article?pii=S0169534703003744 Comment: Exciting as this article seems to be on first reading, the enormous diversity and accompanying pictures refer to the evolution of Drosophila's naughty bits. Posted by Robert Karl Stonjek. --- þ RIMEGate(tm)/RGXPost V1.14 at BBSWORLD * Info{at}bbsworld.com --- * RIMEGate(tm)V10.2áÿ* RelayNet(tm) NNTP Gateway * MoonDog BBS * RgateImp.MoonDog.BBS at 1/15/04 8:39:22 PM* Origin: MoonDog BBS, Brooklyn,NY, 718 692-2498, 1:278/230 (1:278/230) SEEN-BY: 633/267 270 @PATH: 278/230 10/345 106/1 2000 633/267 |
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