增强的互操作性是蚊子直接吸血选择的相关反应

IF 2.3 2区 生物学 Q2 ECOLOGY
Rudyard J. Borowczak, Mary A. Wood, William E. Bradshaw, Peter A. Armbruster, Christina M. Holzapfel
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引用次数: 0

摘要

在此,我们确定了选择对猪笼草蚊子(Wyeomyia smithii Coq)多态种群取血的生活史后果。(双翅目蚊科)。所有的W. smithii种群在不吸血(咬人)的情况下产生第一批卵;南方种群在第二批和随后的批次产卵时需要血餐,但在咬的倾向上是多态的。为了确定直接选择对采血的相关生活史反应,我们比较了专门选择增加采血的品系和未选择的平行维持11代的对照品系之间的繁殖力、成年寿命和生殖分配。以前的研究主要集中在血液喂养对整体繁殖力的健康益处上。在此,我们评估了一种新的适应性益处,即在面临不可预测的可变幼虫环境的种群中,通过将风险分散到多个生殖事件中来降低生殖失败的风险。我们认为,“分散风险”强化了其他节肢动物对取血的选择,在这些节肢动物中,繁殖力与生殖分配在时间或空间上的分离在以前被忽视了。重要的是,“分散风险”的遗传变异应增强病媒能力,并通过减少幼虫来源使病媒控制更加困难。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Enhanced Iteroparity Is a Correlated Response to Direct Selection on Blood Feeding in a Mosquito

Enhanced Iteroparity Is a Correlated Response to Direct Selection on Blood Feeding in a Mosquito

Herein, we determine life-history consequences of selection on blood feeding in a polymorphic population of the pitcher-plant mosquito, Wyeomyia smithii Coq. (Diptera: Culicidae). All populations of W. smithii produce an initial batch of eggs without ever taking a blood meal (biting); southern populations require a blood meal for the second and subsequent batches of eggs, but are polymorphic for propensity to bite. To determine correlated life-history responses to direct selection on blood feeding, we compared fecundity, adult longevity, and reproductive allocation between a line selected specifically for increased blood feeding and its unselected, control line maintained in parallel for 11 generations. Previous studies have focused on the fitness benefits of blood feeding in terms of overall fecundity. Herein, we evaluate a novel fitness benefit of blood feeding that reduces the risk of reproductive failure by spreading that risk across multiple reproductive events in a population confronted with an unpredictably variable larval environment. We propose that “spreading the risk” reinforces selection on blood feeding in other arthropods in which the separation of fecundity from reproductive allocation in time or space has previously been neglected. Importantly, heritable variation for “spreading the risk” should enhance vectorial capacity and make more difficult vector control through larval source reduction.

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来源期刊
CiteScore
4.40
自引率
3.80%
发文量
1027
审稿时长
3-6 weeks
期刊介绍: Ecology and Evolution is the peer reviewed journal for rapid dissemination of research in all areas of ecology, evolution and conservation science. The journal gives priority to quality research reports, theoretical or empirical, that develop our understanding of organisms and their diversity, interactions between them, and the natural environment. Ecology and Evolution gives prompt and equal consideration to papers reporting theoretical, experimental, applied and descriptive work in terrestrial and aquatic environments. The journal will consider submissions across taxa in areas including but not limited to micro and macro ecological and evolutionary processes, characteristics of and interactions between individuals, populations, communities and the environment, physiological responses to environmental change, population genetics and phylogenetics, relatedness and kin selection, life histories, systematics and taxonomy, conservation genetics, extinction, speciation, adaption, behaviour, biodiversity, species abundance, macroecology, population and ecosystem dynamics, and conservation policy.
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