性选择的形式能否解释由不同的交配形态所表达的静态武器异速发育模式?

IF 2.6 2区 环境科学与生态学 Q2 ECOLOGY
Evolution Pub Date : 2025-10-14 DOI:10.1093/evolut/qpaf215
Clint D Kelly
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引用次数: 0

摘要

作用于性状的选择机制预计会塑造其静态异速生长。然而,很少有研究量化作用于野生性状的性选择形式,以测试该性状是否如预测的那样异速生长。甚至很少有研究将表达武器多态性的雄性作为其替代交配策略的一部分来测试这些预测。在这里,我使用实地数据来测试性选择如何影响威灵顿树wētā (H. crasssidens)雄性武器的缩放异形体,威灵顿树是一种新西兰特有的雄性三型和后肢一夫多妻制昆虫。与预测10龄雄性的大型武器在直接性选择下会呈高异速扩张相反,我发现10龄雄性的大型武器不受直接性选择的影响,而是呈低异速扩张。同样,8龄和9龄雄性武器都没有直接的性选择,它们的武器分别是高异速和低异速。我的研究表明,要解开性选择特征尺度模式进化的相互矛盾的假设,必须超越简单的可行性-性选择二分法,还要考虑武器的功能和使用武器的生态环境。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Can the form of sexual selection explain patterns of static weapon allometry expressed by alternative mating morphotypes?

The regime of selection acting on a trait is expected to shape its static allometry. Few studies, however, have quantified the form of sexual selection acting on a trait in the wild to test whether the trait allometrically scales as predicted. Even fewer studies have tested these predictions using males expressing weapon polymorphism as part of their alternative mating strategies. Here, I use field data to test how sexual selection shapes scaling allometries of male weaponry in the Wellington tree wētā (H. crassidens), a male-trimorphic and harem-polygynous insect endemic to New Zealand. Contrary to the prediction that 10th instar males' large weaponry would scale hyperallometrically because it is under direct sexual selection, I found that 10th instar weaponry is not subject to direct sexual selection and scales hypoallometrically. Similarly, neither 8th nor 9th instar male weaponry experiences direct sexual selection, and their weaponry scales hyperallometrically and hypoallometrically, respectively. My study suggests that disentangling competing hypotheses for the evolution of scaling patterns of sexually selected traits must go beyond a simple viability-sexual selection dichotomy by also considering weapon function and the ecological context within which the weapon is used.

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来源期刊
Evolution
Evolution 环境科学-进化生物学
CiteScore
5.00
自引率
9.10%
发文量
0
审稿时长
3-6 weeks
期刊介绍: Evolution, published for the Society for the Study of Evolution, is the premier publication devoted to the study of organic evolution and the integration of the various fields of science concerned with evolution. The journal presents significant and original results that extend our understanding of evolutionary phenomena and processes.
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