火灾后热带泥炭地甲烷通量的升高与泥炭微生物群集的深度变化有关。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-01-23 DOI:10.1038/s41522-024-00478-9
Aditya Bandla, Hasan Akhtar, Massimo Lupascu, Rahayu Sukmaria Sukri, Sanjay Swarup
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引用次数: 0

摘要

热带泥炭地的火灾会向深处延伸,将泥炭地从碳汇转变为甲烷源,严重限制了森林的恢复。泥炭微生物群影响着碳转化和森林恢复,但目前我们对火灾后微生物群变化的了解还很有限。我们之前的研究强调了热带泥炭地火灾后泥炭表面、地下水位、地上植被和甲烷通量之间关系的改变。在这里,我们将这些变化与火灾后泥炭微生物群组成和组装过程在不同深度的变化联系起来。我们报告了火灾后α多样性的变化,这种变化具有王国特异性和深度依赖性,在较深的地方差异很大。相反,我们发现微生物组的组成在所有深度都发生了变化。组成的变化延伸到了参与甲烷转化的功能群,在中层和深层,甲烷生物富集,而甲烷营养生物减少。最后,我们表明,深层群落的变化是与火灾后水文和地上植被变化相关的同质选择的结果。总之,我们的研究结果为之前报道的火灾后甲烷通量提供了生物学基础,并为微生物组的组装过程随深度的变化提供了新的见解,而微生物组的组装过程是生态系统功能可预测性和生态系统恢复的最终基础。
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Elevated methane flux in a tropical peatland post-fire is linked to depth-dependent changes in peat microbiome assembly.

Fires in tropical peatlands extend to depth, transforming them from carbon sinks into methane sources and severely limit forest recovery. Peat microbiomes influence carbon transformations and forest recovery, yet our understanding of microbiome shifts post-fire is currently limited. Our previous study highlighted altered relationships between the peat surface, water table, aboveground vegetation, and methane flux after fire in a tropical peatland. Here, we link these changes to post-fire shifts in peat microbiome composition and assembly processes across depth. We report kingdom-specific and depth-dependent shifts in alpha diversity post-fire, with large differences at deeper depths. Conversely, we found shifts in microbiome composition across all depths. Compositional shifts extended to functional groups involved in methane turnover, with methanogens enriched and methanotrophs depleted at mid and deeper depths. Finally, we show that community shifts at deeper depths result from homogeneous selection associated with post-fire changes in hydrology and aboveground vegetation. Collectively, our findings provide a biological basis for previously reported methane fluxes after fire and offer new insights into depth-dependent shifts in microbiome assembly processes, which ultimately underlie ecosystem function predictability and ecosystem recovery.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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