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Aquatic microfauna alter larval food resources and affect development and biomass of West Nile and Saint Louis encephalitis vector Culex nigripalpus (Diptera: Culicidae)

机译:水生小动物改变幼虫的食物资源并影响西尼罗河和圣路易斯脑炎病媒库蚊(Dilexera:Culicidae)的发育和生物量

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摘要

Ciliate protists and rotifers are ubiquitous in aquatic habitats and can comprise a significant portion of the microbial food resources available to larval mosquitoes, often showing substantial declines in abundance in the presence of mosquito larvae. This top‐down regulation of protists is reported to be strong for mosquitoes inhabiting small aquatic containers such as pitcher plants or tree holes, but the nature of these interactions with larval mosquitoes developing in other aquatic habitats is poorly understood. We examined the effects of these two microbial groups on lower trophic level microbial food resources, such as bacteria, small flagellates, and organic particles, in the water column, and on Culex larval development and adult production. In three independent laboratory experiments using two microeukaryote species (one ciliate protist and one rotifer) acquired from field larval mosquito habitats and cultured in the laboratory, we determined the effects of Culex nigripalpus larval grazing on water column microbial dynamics, while simultaneously monitoring larval growth and development. The results revealed previously unknown interactions that were different from the top‐down regulation of microbial groups by mosquito larvae in other systems. Both ciliates and rotifers, singly or in combination, altered other microbial populations and inhibited mosquito growth. It is likely that these microeukaryotes, instead of serving as food resources, competed with early instar mosquito larvae for microbes such as small flagellates and bacteria in a density‐dependent manner. These findings help our understanding of the basic larval biology of Culex mosquitoes, variation in mosquito production among various larval habitats, and may have implications for existing vector control strategies and for developing novel microbial‐based control methods.
机译:纤毛虫和轮虫在水生生境中无处不在,可占幼虫蚊子微生物食物资源的很大一部分,在存在蚊虫幼虫的情况下,其丰度通常会显着下降。据报道,这种对生物的自上而下的监管对于居住在小型水生容器(如捕虫笼或树洞)中的蚊子有很强的控制作用,但人们对与其他水生生境中发育的幼虫的相互作用的本质了解甚少。我们检查了这两个微生物群对水柱中营养级别较低的微生物食物资源(如细菌,小鞭毛和有机颗粒)以及库蚊幼虫发育和成年生产的影响。在三个独立的实验室实验中,使用了从田间幼虫蚊子栖息地获取并在实验室中培养的两种微真核生物物种(一种纤毛虫和一种轮虫),我们确定了黑头库蚊幼虫放牧对水柱微生物动力学的影响,同时监测了幼虫的生长和发展。结果揭示了以前未知的相互作用,这与其他系统中的蚊子幼虫自上而下对微生物群的调节不同。纤毛和轮虫单独或组合地改变了其他微生物的种群并抑制了蚊子的生长。这些微真核生物可能不作为食物资源,而是以幼龄蚊子幼虫以密度依赖的方式与微生物如小鞭毛和细菌竞争。这些发现有助于我们了解库蚊的基本幼虫生物学,各种幼虫栖息地之间蚊虫生产的变化,并且可能对现有的媒介控制策略和开发新的基于微生物的控制方法有影响。

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