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The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession

The Northern high latitudes are warming twice as fast as the global average, and permafrost has become vulnerable to thaw. Changes to the environment during thaw leads to shifts in microbial communities and their associated functions, such as greenhouse gas emissions. Understanding the ecological pr...

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Autores principales: Doherty, Stacey Jarvis, Barbato, Robyn A., Grandy, A. Stuart, Thomas, W. Kelley, Monteux, Sylvain, Dorrepaal, Ellen, Johansson, Margareta, Ernakovich, Jessica G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691490/
https://www.ncbi.nlm.nih.gov/pubmed/33281795
http://dx.doi.org/10.3389/fmicb.2020.596589
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author Doherty, Stacey Jarvis
Barbato, Robyn A.
Grandy, A. Stuart
Thomas, W. Kelley
Monteux, Sylvain
Dorrepaal, Ellen
Johansson, Margareta
Ernakovich, Jessica G.
author_facet Doherty, Stacey Jarvis
Barbato, Robyn A.
Grandy, A. Stuart
Thomas, W. Kelley
Monteux, Sylvain
Dorrepaal, Ellen
Johansson, Margareta
Ernakovich, Jessica G.
author_sort Doherty, Stacey Jarvis
collection PubMed
description The Northern high latitudes are warming twice as fast as the global average, and permafrost has become vulnerable to thaw. Changes to the environment during thaw leads to shifts in microbial communities and their associated functions, such as greenhouse gas emissions. Understanding the ecological processes that structure the identity and abundance (i.e., assembly) of pre- and post-thaw communities may improve predictions of the functional outcomes of permafrost thaw. We characterized microbial community assembly during permafrost thaw using in situ observations and a laboratory incubation of soils from the Storflaket Mire in Abisko, Sweden, where permafrost thaw has occurred over the past decade. In situ observations indicated that bacterial community assembly was driven by randomness (i.e., stochastic processes) immediately after thaw with drift and dispersal limitation being the dominant processes. As post-thaw succession progressed, environmentally driven (i.e., deterministic) processes became increasingly important in structuring microbial communities where homogenizing selection was the only process structuring upper active layer soils. Furthermore, laboratory-induced thaw reflected assembly dynamics immediately after thaw indicated by an increase in drift, but did not capture the long-term effects of permafrost thaw on microbial community dynamics. Our results did not reflect a link between assembly dynamics and carbon emissions, likely because respiration is the product of many processes in microbial communities. Identification of dominant microbial community assembly processes has the potential to improve our understanding of the ecological impact of permafrost thaw and the permafrost–climate feedback.
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spelling pubmed-76914902020-12-04 The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession Doherty, Stacey Jarvis Barbato, Robyn A. Grandy, A. Stuart Thomas, W. Kelley Monteux, Sylvain Dorrepaal, Ellen Johansson, Margareta Ernakovich, Jessica G. Front Microbiol Microbiology The Northern high latitudes are warming twice as fast as the global average, and permafrost has become vulnerable to thaw. Changes to the environment during thaw leads to shifts in microbial communities and their associated functions, such as greenhouse gas emissions. Understanding the ecological processes that structure the identity and abundance (i.e., assembly) of pre- and post-thaw communities may improve predictions of the functional outcomes of permafrost thaw. We characterized microbial community assembly during permafrost thaw using in situ observations and a laboratory incubation of soils from the Storflaket Mire in Abisko, Sweden, where permafrost thaw has occurred over the past decade. In situ observations indicated that bacterial community assembly was driven by randomness (i.e., stochastic processes) immediately after thaw with drift and dispersal limitation being the dominant processes. As post-thaw succession progressed, environmentally driven (i.e., deterministic) processes became increasingly important in structuring microbial communities where homogenizing selection was the only process structuring upper active layer soils. Furthermore, laboratory-induced thaw reflected assembly dynamics immediately after thaw indicated by an increase in drift, but did not capture the long-term effects of permafrost thaw on microbial community dynamics. Our results did not reflect a link between assembly dynamics and carbon emissions, likely because respiration is the product of many processes in microbial communities. Identification of dominant microbial community assembly processes has the potential to improve our understanding of the ecological impact of permafrost thaw and the permafrost–climate feedback. Frontiers Media S.A. 2020-11-13 /pmc/articles/PMC7691490/ /pubmed/33281795 http://dx.doi.org/10.3389/fmicb.2020.596589 Text en Copyright © 2020 Doherty, Barbato, Grandy, Thomas, Monteux, Dorrepaal, Johansson and Ernakovich. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Doherty, Stacey Jarvis
Barbato, Robyn A.
Grandy, A. Stuart
Thomas, W. Kelley
Monteux, Sylvain
Dorrepaal, Ellen
Johansson, Margareta
Ernakovich, Jessica G.
The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession
title The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession
title_full The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession
title_fullStr The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession
title_full_unstemmed The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession
title_short The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession
title_sort transition from stochastic to deterministic bacterial community assembly during permafrost thaw succession
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7691490/
https://www.ncbi.nlm.nih.gov/pubmed/33281795
http://dx.doi.org/10.3389/fmicb.2020.596589
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