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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Main Authors: Stacey Jarvis Doherty, Robyn A. Barbato, A. Stuart Grandy, W. Kelley Thomas, Sylvain Monteux, Ellen Dorrepaal, Margareta Johansson, Jessica G. Ernakovich
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmicb.2020.596589/full
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author Stacey Jarvis Doherty
Stacey Jarvis Doherty
Robyn A. Barbato
A. Stuart Grandy
W. Kelley Thomas
Sylvain Monteux
Ellen Dorrepaal
Margareta Johansson
Jessica G. Ernakovich
Jessica G. Ernakovich
author_facet Stacey Jarvis Doherty
Stacey Jarvis Doherty
Robyn A. Barbato
A. Stuart Grandy
W. Kelley Thomas
Sylvain Monteux
Ellen Dorrepaal
Margareta Johansson
Jessica G. Ernakovich
Jessica G. Ernakovich
author_sort Stacey Jarvis Doherty
collection DOAJ
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 doaj.art-7ef3b27df26d4be9a3c0d3bfe3f3f0762022-12-22T00:15:57ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2020-11-011110.3389/fmicb.2020.596589596589The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw SuccessionStacey Jarvis Doherty0Stacey Jarvis Doherty1Robyn A. Barbato2A. Stuart Grandy3W. Kelley Thomas4Sylvain Monteux5Ellen Dorrepaal6Margareta Johansson7Jessica G. Ernakovich8Jessica G. Ernakovich9Department of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH, United StatesCold Regions Research and Engineering Laboratory, Engineer Research Development Center, United States Army Corps of Engineers, Hanover, NH, United StatesCold Regions Research and Engineering Laboratory, Engineer Research Development Center, United States Army Corps of Engineers, Hanover, NH, United StatesDepartment of Natural Resources and the Environment, University of New Hampshire, Durham, NH, United StatesDepartment of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH, United StatesDepartment of Soil and Environment, Swedish University of Agricultural Sciences, Uppsala, SwedenClimate Impacts Research Centre, Department of Ecology and Environmental Sciences, Umeå University, Abisko, SwedenDepartment of Physical Geography and Ecosystem Science, Lund University, Lund, SwedenDepartment of Molecular, Cellular, and Biomedical Sciences, University of New Hampshire, Durham, NH, United StatesDepartment of Natural Resources and the Environment, University of New Hampshire, Durham, NH, United StatesThe 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.https://www.frontiersin.org/articles/10.3389/fmicb.2020.596589/fullpermafrost thawmicrobial communitycommunity assemblyphylogenetic null modelingecological processes
spellingShingle Stacey Jarvis Doherty
Stacey Jarvis Doherty
Robyn A. Barbato
A. Stuart Grandy
W. Kelley Thomas
Sylvain Monteux
Ellen Dorrepaal
Margareta Johansson
Jessica G. Ernakovich
Jessica G. Ernakovich
The Transition From Stochastic to Deterministic Bacterial Community Assembly During Permafrost Thaw Succession
Frontiers in Microbiology
permafrost thaw
microbial community
community assembly
phylogenetic null modeling
ecological processes
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 permafrost thaw
microbial community
community assembly
phylogenetic null modeling
ecological processes
url https://www.frontiersin.org/articles/10.3389/fmicb.2020.596589/full
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