森林属多样性沿纬度梯度的超寄生空间格局:来自云杉芽虫-拟寄生物群落的启示。

IF 1.8 3区 农林科学 Q2 ENTOMOLOGY Environmental Entomology Pub Date : 2024-02-20 DOI:10.1093/ee/nvad110
Simon Legault, Patrick M A James
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引用次数: 0

摘要

高阶移动捕食者通常被认为增加了生态系统的稳定性和对自然扰动的恢复能力。在许多昆虫食物网中,寄生蜂占据着较高的营养地位,寄生蜂本身是超寄生蜂的宿主,这可以降低初级寄生蜂控制害虫的效率。因此,类超寄生物可以通过促进害虫爆发而对生态系统造成损害,或者通过在较长时间内稳定食物网波动而对生态系统提供服务。为了更好地了解高寄生性如何影响多营养森林系统,我们首次研究了云杉芽虫高寄生性的空间变化。研究了云杉budworm暴发期间常见的2种主要寄主(Apanteles fumiferanae和Glypta fumiferanae),并在森林属多样性纬度梯度(超过450 km)的28个地点估算了2014-2015年云杉budworm的真寄生率和假高寄生率。利用dna条形码技术对超寄生蜂的隐性多样性进行了定量分析。研究发现,云杉芽虫和云杉芽虫在5种常见的高寄生性物种中至少有2种是相同的,这证实了云杉芽虫-寄生性食物网的关联性。此外,高寄生性受空间环境的调节,我们观察到森林属多样性与烟蚜的高寄生性呈正相关,而烟蚜的高寄生性与森林属多样性呈正相关。进一步监测超寄生现象具有重要的潜力,可以为了解森林成分如何影响多营养相互作用和时空爆发动态提供新的见解。
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Spatial patterns of hyperparasitism along a latitudinal gradient of forest genus diversity: insights from the spruce budworm-parasitoids community.

High-order mobile predators are generally thought to increase ecosystem stability and resilience to natural perturbations. In many insect food-webs, higher trophic positions are occupied by parasitoids, which are themselves hosts for hyperparasitoids that can reduce primary parasitoids' efficiency in controlling insect pests. Hyperparasitoids can thus provide ecosystem disservices by facilitating pest outbreaks, or ecosystem services by stabilizing food web fluctuations over longer time periods. To better understand how hyperparasitism affects multitrophic forest systems, we examined for the first time spatial variations in hyperparasitism associated with the spruce budworm. We examined 2 common primary parasitoids of the spruce budworm during outbreaks (Apanteles fumiferanae and Glypta fumiferanae), and estimated their true and pseudohyperparasitism rates in 2014-2015 from 28 locations across a latitudinal gradient (over 450 km) of forest genus diversity. Hyperparasitoid cryptic diversity was also quantified using DNA-barcoding. We found that A. fumiferanae and G. fumiferanae share at least 2 of 5 common hyperparasitoid species, confirming the connected nature of the spruce budworm-parasitoid food web. Moreover, hyperparasitism is modulated by spatial context as we observed a positive correlation between forest genus diversity and hyperparasitism for A. fumiferanae, but not for G. fumiferanae. Further monitoring hyperparasitism holds significant potential to provide new insights into how forest composition affects multitrophic interactions and spatio-temporal outbreak dynamics.

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来源期刊
Environmental Entomology
Environmental Entomology 生物-昆虫学
CiteScore
3.90
自引率
5.90%
发文量
97
审稿时长
3-8 weeks
期刊介绍: Environmental Entomology is published bimonthly in February, April, June, August, October, and December. The journal publishes reports on the interaction of insects with the biological, chemical, and physical aspects of their environment. In addition to research papers, Environmental Entomology publishes Reviews, interpretive articles in a Forum section, and Letters to the Editor.
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