性大小和形状的二态性与预测一致,即自然和性选择都推动了摩门教蟋蟀(Anabrus simplex)两性二态性的进化。

IF 2.3 Q2 ECOLOGY
Kevin A Judge, Stacy R Demma, Laura J Robson, Patrick D Lorch, Christopher J Vinyard, Darryl T Gwynne
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引用次数: 0

摘要

背景:选择是导致种群形态适应的强大力量。我们测试了关于自然选择和性选择在塑造摩尔门蟋蟀(Anabrus simplex)形态中的作用的预测,这种物种有两种不同的种群类型,它们的生态条件不同。独居种群的特点是低密度、非迁徙个体和典型的交配角色(雄性为获得挑剔的雌性而竞争),而群居种群的特点是高密度、迁徙行为、相反的交配角色和广泛的同类相食。我们从独居和群居的种群中收集了个体——以它们的行为而不是形态为特征——并测量了几种形态特征。我们将这些特征转化为形状变量,通过将每个测量除以代表身体尺寸的几个度量维度的几何平均值。我们在大小和形状变量中测试了种群类型和性别差异,并在几个性别限制的形状变量中测试了种群类型差异。我们还使用判别函数分析来测试一个先前神秘的种群,发现它在遗传上像群居种群,但表现出许多方面的独居种群行为,在形态上更像独居种群还是群居种群。我们的分析用于确定将标本分配到正确种群类型所需的最小测量次数。结果:群居种群体型大于独居种群,两种种群类型中雌性均大于雄性。这种性别大小二态性在独居种群中更为明显。独居种群和群居种群表现出其他几种形状差异以及形状性别二态性程度的差异。这个神秘的种群在形态上被明确地归类为更像群居种群,这一发现与先前的研究结果一致,即与群居种群的遗传相似性。头宽始终是区分两个种群成员的最佳性状。结论:性别大小和形状二态性的模式与预测一致,即自然选择和性选择共同推动了摩门教蟋蟀性别二态性的进化。未来的工作应该测量雄性和雌性在独居和群居种群中选择的方向和形状,特别关注头部形状。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sexual size and shape dimorphism are consistent with predictions that both natural and sexual selection are driving the evolution of sexual dimorphism in Mormon crickets, Anabrus simplex.

Background: Selection can be a powerful force causing morphological adaptation in populations. We tested predictions about the role of both natural and sexual selection in shaping morphology in the Mormon cricket, Anabrus simplex, a species with two population types that differ in their ecological conditions. Solitary populations are characterized by low densities, non-migratory individuals, and typical mating roles (males compete for access to choosy females), whereas gregarious populations are characterized by high densities, migratory behaviour, reversed mating roles, and widespread cannibalism. We collected individuals from both solitary and gregarious populations - characterized by their behaviour and not morphology - and measured several morphological traits. We transformed these traits to shape variables by dividing each measurement by a geometric mean of several metric dimensions representing body size. We tested for population type and sex differences in size and shape variables, and we tested for population type differences in several sex-limited shape variables. We also used discriminant function analysis to test whether a previously enigmatic population, found to be genetically like gregarious populations, but exhibiting many aspects of solitary population behaviour, was morphologically more like solitary or gregarious populations. Our analysis was used to determine the minimum number of measurements needed to assign specimens to the correct population type.

Results: We found that gregarious populations were larger in body size than solitary populations and that females were larger than males in both population types. This sexual size dimorphism was more pronounced in solitary populations. Solitary and gregarious populations displayed several other shape differences as well as differences in the degree of sexual dimorphism in shape. The enigmatic population was unambiguously classified as morphologically more like gregarious populations, a finding which agrees with previous work showing genetic similarities with gregarious populations. Head width was consistently the best character to distinguish members of both populations.

Conclusions: Patterns of sexual size and shape dimorphism are consistent with predictions that both natural and sexual selection are driving the evolution of sexual dimorphism in Mormon crickets. Future work should measure the direction and shape of selection on both males and females in solitary and gregarious populations, focusing particular attention on head shape.

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