万物无处不在吗?扩散限制对甲烷化菌群落功能的影响

IF 4 2区 生物学 Q2 MICROBIOLOGY
Jie Fang, Yongcui Deng, Zihao Liu, Jonathan M. Adams
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引用次数: 0

摘要

微生物生态学和生物地理学中扩散限制的意义仍然存在争议。我们的目的是澄清扩散限制在甲烷化菌群落适应盐胁迫中的作用,本质上是在功能方面测试“万物皆有”的假设。收集了长江沿岸不同地理距离的河岸沉积物和离长江内陆不同地理距离的湖滨沉积物。用~5% CH4在盐度为50 g/L、盐度为50 g/L加甲烷化菌群落接种量和对照三种条件下培养微生物。我们观察到盐度增加时甲烷氧化的显著延迟,但耐盐甲烷营养活性在河岸沉积物中持续存在。利用DNA-SIP技术,我们鉴定出了可能来自咸水河口的耐盐甲基杆菌类群。而在远离长江的内陆湖泊/池塘中,在高盐度条件下,不接种氧化甲烷的样本逐渐减少,直到130公里的距离,没有样本能够适应。通过接种含盐长江三角洲的繁殖体,在所有情况下均恢复了甲烷化,证实了耐盐甲基杆菌繁殖体扩散限制对生态系统功能适应的影响。通过关注生态系统功能而不仅仅是分类群落,本研究独特地测试了微生物生态学的一个关键范式,表明大规模微生物扩散限制可以限制生态系统的适应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Is Everything Everywhere? Dispersal Limitation Impacts Methanotroph Community Functioning

Is Everything Everywhere? Dispersal Limitation Impacts Methanotroph Community Functioning

Is Everything Everywhere? Dispersal Limitation Impacts Methanotroph Community Functioning

Is Everything Everywhere? Dispersal Limitation Impacts Methanotroph Community Functioning

Is Everything Everywhere? Dispersal Limitation Impacts Methanotroph Community Functioning

The significance of dispersal limitation in microbial ecology and biogeography remains debated. We aimed to clarify the role of dispersal limitation in the adaptation of methanotroph communities to salt-stress, essentially testing the ‘everything is everywhere’ hypothesis in functional terms. Riparian sediments along the Yangtze River and lakeshore sediments at varying geographical distances inland from the river were collected. Microcosms were incubated with ~5% CH4 under three conditions: 50 g/L salinity, 50 g/L salinity plus a methanotroph community inoculum, and a control. We observed a significant delay in methane oxidation at increased salinity, but salt-tolerant methanotrophic activity persisted in riparian sediments. Using DNA-SIP, we identified halotolerant Methylobacter-taxa that possibly dispersed from the saline estuary. By contrast, in lakes/ponds inland away from the Yangtze, progressively fewer samples oxidised methane under high salinity without inoculation, until at 130 km distance, no samples could adapt. Methanotrophy was restored in every case by inoculation with propagules from the saline Yangtze Delta, confirming the impact of dispersal limitation of halotolerant Methylobacter-propagules in constraining ecosystem functional adaptation. By focusing on ecosystem functions rather than just taxonomic communities, this study uniquely tests a key paradigm in microbial ecology, suggesting that broad-scale microbial dispersal limitation can constrain ecosystem adaptation.

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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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