Gay L, Eady P E, Vasudev R, Hosken D J, Tregenza T
Centre for Ecology and Conservation, University of Exeter, Cornwall, Tremough Campus, Penryn TR10 9EZ, UK.
Biol Lett. 2009 Oct 23;5(5):693-6. doi: 10.1098/rsbl.2009.0072. Epub 2009 Apr 1.
Sexual conflict over reproductive investment can lead to sexually antagonistic coevolution and reproductive isolation. It has been suggested that, unlike most models of allopatric speciation, the evolution of reproductive isolation through sexually antagonistic coevolution will occur faster in large populations as these harbour greater levels of standing genetic variation, receive larger numbers of mutations and experience more intense sexual selection. We tested this in bruchid beetle populations (Callosobruchus maculatus) by manipulating population size and standing genetic variability in replicated lines derived from founders that had been released from sexual conflict for 90 generations. We found that after 19 generations of reintroduced sexual conflict, none of our treatments had evolved significant overall reproductive isolation among replicate lines. However, as predicted, measures of reproductive isolation tended to be greater among larger populations. We discuss our methodology, arguing that reproductive isolation is best examined by performing a matrix of allopatric and sympatric crosses whereas measurement of divergence requires crosses with a tester line.
生殖投资方面的性冲突会导致性对抗性协同进化和生殖隔离。有人提出,与大多数异域物种形成模型不同,通过性对抗性协同进化实现生殖隔离的进化在大种群中会更快发生,因为这些种群拥有更高水平的现存遗传变异、接收更多的突变并且经历更强烈的性选择。我们通过操纵源自已经从性冲突中释放90代的奠基者的重复品系中的种群大小和现存遗传变异性,在豆象甲虫种群(四纹豆象)中对此进行了测试。我们发现,在重新引入性冲突19代后,我们的任何处理在重复品系之间都没有进化出显著的总体生殖隔离。然而,正如预测的那样,生殖隔离的测量值在较大种群中往往更大。我们讨论了我们的方法,认为通过进行异域和同域杂交的矩阵来最好地检验生殖隔离,而分歧的测量则需要与测试品系进行杂交。