Environmental filtering governs consistent vertical zonation in sedimentary microbial communities across disconnected mountain lakes

IF 4.3 2区 生物学 Q2 MICROBIOLOGY Environmental microbiology Pub Date : 2024-03-13 DOI:10.1111/1462-2920.16607
Jordan M. Von Eggers, Nathan I. Wisnoski, John W. Calder, Eric Capo, Dulcinea V. Groff, Amy C. Krist, Bryan Shuman
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Abstract

Subsurface microorganisms make up the majority of Earth's microbial biomass, but ecological processes governing surface communities may not explain community patterns at depth because of burial. Depth constrains dispersal and energy availability, and when combined with geographic isolation across landscapes, may influence community assembly. We sequenced the 16S rRNA gene of bacteria and archaea from 48 sediment cores across 36 lakes in four disconnected mountain ranges in Wyoming, USA and used null models to infer assembly processes across depth, spatial isolation, and varying environments. Although we expected strong dispersal limitations across these isolated settings, community composition was primarily shaped by environmental selection. Communities consistently shifted from domination by organisms that degrade organic matter at the surface to methanogenic, low-energy adapted taxa in deeper zones. Stochastic processes—like dispersal limitation—contributed to differences among lakes, but because these effects weakened with depth, selection processes ultimately governed subsurface microbial biogeography.

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环境过滤作用于互不相连的高山湖泊中沉积微生物群落的一致垂直分带。
地表下微生物占地球微生物生物量的大部分,但由于埋藏的原因,管理地表群落的生态过程可能无法解释深层的群落模式。深度限制了传播和能量的可用性,再加上地貌上的地理隔离,可能会影响群落的组合。我们对美国怀俄明州四个互不相连的山脉中 36 个湖泊的 48 个沉积物岩心中的细菌和古细菌的 16S rRNA 基因进行了测序,并利用空模型推断了不同深度、空间隔离和不同环境下的群落组装过程。尽管我们预计在这些与世隔绝的环境中生物的扩散会受到很大限制,但群落的组成主要是由环境选择决定的。群落一直从由地表降解有机物的生物主导转向深层区域的产甲烷、低能量适应类群。随机过程--如扩散限制--导致了湖泊之间的差异,但由于这些影响随着深度的增加而减弱,因此选择过程最终决定了地下微生物生物地理学。
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来源期刊
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
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