Host selection in insects: reproductive interference shapes behavior of ovipositing females

Host selection in insects: reproductive interference shapes behavior of ovipositing females
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昆虫的宿主选择:生殖干扰塑造排卵雌性的行为

DOI:
10.1007/s10144-015-0491-4
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发表时间:
2015
期刊:
影响因子:
1.7
通讯作者:
Suzuki Noriyuki
Suzuki Noriyuki
中科院分区:
环境科学与生态学3区
文献类型:
--
作者:
Sogabe;A.;Takata;H. & Kato;S.;Suzuki Noriyuki

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在自然界中,亲缘关系密切的物种往往利用不同的寄主物种,但目前尚不清楚是什么因素促成了这种多样化寄主选择的进化和维持。在这篇综述中,我描述了负的种间交配相互作用(生殖干扰)如何影响动物的寄主选择,主要集中在植食性和掠食性昆虫上。首先,我解释了这个假设的一个重要前提,那就是成人的繁殖地点与后代的喂养地点是相同的。接下来,我描述了几个数学模型和经过充分研究的经验系统,以表明生殖干扰可以充分驱动和维持系统发育相关物种之间不同的宿主选择。然后,我首次提出,生殖干扰可能导致昆虫的产卵偏好,这对后代的生存和发展不是最优的,因为母亲的适应性行为最大化了母亲自己的适应性。此外,我认为,在昆虫中,生殖干扰可能在雌性落在寄主上之前塑造了产卵行为(例如,栖息地偏好),而不影响落在寄主上后的决策。我想强调的是,这两个论点代表了阐明复杂昆虫产卵行为模式的新方法。
In nature, closely related species often utilize different host species, but it is still unclear what factors contribute to the evolution and maintenance of such diversified host selection. In this review, I describe how negative interspecific mating interactions (reproductive interference) can shape host selection by animals, focusing mainly on phytophagous and predatory insects. First, I explain an important premise of this hypothesis, which is that the adult reproductive site is the same as the feeding site for the offspring. Next, I describe several mathematical models and well-studied empirical systems to show that reproductive interference can sufficiently drive and maintain different host selection between phylogenetically related species. Then, I argue for the first time that reproductive interference can cause an oviposition preference in insects that is not optimal for the survival and development of the offspring, as a result of maternal adaptive behavior that maximizes the mother’s own fitness. Furthermore, I argue that in insects, reproductive interference probably shapes oviposition behavior before the female alights on the host (e.g., habitat preference), without affecting post-alighting decision making. I would like to emphasize that these two arguments represent the novel approach to clarify the unrevealed pattern of complex insect oviposition behavior.
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