Life At The Frozen Limit: Microbial Carbon Metabolism Across A Late Pleistocene Permafrost Chronosequence

Permafrost is an extreme habitat yet it hosts microbial populations that remain active over millennia. Using permafrost collected from a Pleistocene chronosequence (19 to 33 ka), we hypothesized that the functional genetic potential of microbial communities in permafrost would reflect microbial stra...

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Published in:Frontiers in Microbiology
Other Authors: Leewis, Mary-Cathrine (author), Berlemont, Renaud (author), Podgorski, David C. (author), Srinivas, Archana (author), Zito, Phoebe (author), Spencer, Robert G. M. (author), McFarland, Jack (author), Douglas, Thomas A. (author), Conaway, Christopher H. (author), Waldrop, Mark (author), Mackelprang, Rachel (author)
Format: Article in Journal/Newspaper
Language:English
Published: 2020
Subjects:
Online Access:https://doi.org/10.3389/fmicb.2020.01753
https://diginole.lib.fsu.edu/islandora/object/fsu%3A774883/datastream/TN/view/Life%20At%20The%20Frozen%20Limit.jpg
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spelling ftfloridasu:oai:diginole.lib.fsu.edu:fsu_774883 2024-06-09T07:48:55+00:00 Life At The Frozen Limit: Microbial Carbon Metabolism Across A Late Pleistocene Permafrost Chronosequence Leewis, Mary-Cathrine (author) Berlemont, Renaud (author) Podgorski, David C. (author) Srinivas, Archana (author) Zito, Phoebe (author) Spencer, Robert G. M. (author) McFarland, Jack (author) Douglas, Thomas A. (author) Conaway, Christopher H. (author) Waldrop, Mark (author) Mackelprang, Rachel (author) 2020-07-29 computer online resource 1 online resource application/pdf https://doi.org/10.3389/fmicb.2020.01753 https://diginole.lib.fsu.edu/islandora/object/fsu%3A774883/datastream/TN/view/Life%20At%20The%20Frozen%20Limit.jpg English eng Frontiers in Microbiology--1664-302X fsu:774883 iid: FSU_libsubv1_wos_000561537000001 doi:10.3389/fmicb.2020.01753 https://diginole.lib.fsu.edu/islandora/object/fsu%3A774883/datastream/TN/view/Life%20At%20The%20Frozen%20Limit.jpg Text journal article 2020 ftfloridasu https://doi.org/10.3389/fmicb.2020.01753 2024-05-10T08:08:08Z Permafrost is an extreme habitat yet it hosts microbial populations that remain active over millennia. Using permafrost collected from a Pleistocene chronosequence (19 to 33 ka), we hypothesized that the functional genetic potential of microbial communities in permafrost would reflect microbial strategies to metabolize permafrost soluble organic matter (OM)in situover geologic time. We also hypothesized that changes in the metagenome across the chronosequence would correlate with shifts in carbon chemistry, permafrost age, and paleoclimate at the time of permafrost formation. We combined high-resolution characterization of water-soluble OM by Fourier-transform ion-cyclotron-resonance mass spectrometry (FT-ICR MS), quantification of organic anions in permafrost water extracts, and metagenomic sequencing to better understand the relationships between the molecular-level composition of potentially bioavailable OM, the microbial community, and permafrost age. Both age and paleoclimate had marked effects on both the molecular composition of dissolved OM and the microbial community. The relative abundance of genes associated with hydrogenotrophic methanogenesis, carbohydrate active enzyme families, nominal oxidation state of carbon (NOSC), and number of identifiable molecular formulae significantly decreased with increasing age. In contrast, genes associated with fermentation of short chain fatty acids (SCFAs), the concentration of SCFAs and ammonium all significantly increased with age. We present a conceptual model of microbial metabolism in permafrost based on fermentation of OM and the buildup of organic acids that helps to explain the unique chemistry of ancient permafrost soils. These findings imply long-termin situmicrobial turnover of ancient permafrost OM and that this pooled biolabile OM could prime ancient permafrost soils for a larger and more rapid microbial response to thaw compared to younger permafrost soils. carbon, dynamics, dissolved organic-matter, vegetation, reveals, temperature, soils, ... Article in Journal/Newspaper permafrost Florida State University: DigiNole Commons Frontiers in Microbiology 11
institution Open Polar
collection Florida State University: DigiNole Commons
op_collection_id ftfloridasu
language English
description Permafrost is an extreme habitat yet it hosts microbial populations that remain active over millennia. Using permafrost collected from a Pleistocene chronosequence (19 to 33 ka), we hypothesized that the functional genetic potential of microbial communities in permafrost would reflect microbial strategies to metabolize permafrost soluble organic matter (OM)in situover geologic time. We also hypothesized that changes in the metagenome across the chronosequence would correlate with shifts in carbon chemistry, permafrost age, and paleoclimate at the time of permafrost formation. We combined high-resolution characterization of water-soluble OM by Fourier-transform ion-cyclotron-resonance mass spectrometry (FT-ICR MS), quantification of organic anions in permafrost water extracts, and metagenomic sequencing to better understand the relationships between the molecular-level composition of potentially bioavailable OM, the microbial community, and permafrost age. Both age and paleoclimate had marked effects on both the molecular composition of dissolved OM and the microbial community. The relative abundance of genes associated with hydrogenotrophic methanogenesis, carbohydrate active enzyme families, nominal oxidation state of carbon (NOSC), and number of identifiable molecular formulae significantly decreased with increasing age. In contrast, genes associated with fermentation of short chain fatty acids (SCFAs), the concentration of SCFAs and ammonium all significantly increased with age. We present a conceptual model of microbial metabolism in permafrost based on fermentation of OM and the buildup of organic acids that helps to explain the unique chemistry of ancient permafrost soils. These findings imply long-termin situmicrobial turnover of ancient permafrost OM and that this pooled biolabile OM could prime ancient permafrost soils for a larger and more rapid microbial response to thaw compared to younger permafrost soils. carbon, dynamics, dissolved organic-matter, vegetation, reveals, temperature, soils, ...
author2 Leewis, Mary-Cathrine (author)
Berlemont, Renaud (author)
Podgorski, David C. (author)
Srinivas, Archana (author)
Zito, Phoebe (author)
Spencer, Robert G. M. (author)
McFarland, Jack (author)
Douglas, Thomas A. (author)
Conaway, Christopher H. (author)
Waldrop, Mark (author)
Mackelprang, Rachel (author)
format Article in Journal/Newspaper
title Life At The Frozen Limit: Microbial Carbon Metabolism Across A Late Pleistocene Permafrost Chronosequence
spellingShingle Life At The Frozen Limit: Microbial Carbon Metabolism Across A Late Pleistocene Permafrost Chronosequence
title_short Life At The Frozen Limit: Microbial Carbon Metabolism Across A Late Pleistocene Permafrost Chronosequence
title_full Life At The Frozen Limit: Microbial Carbon Metabolism Across A Late Pleistocene Permafrost Chronosequence
title_fullStr Life At The Frozen Limit: Microbial Carbon Metabolism Across A Late Pleistocene Permafrost Chronosequence
title_full_unstemmed Life At The Frozen Limit: Microbial Carbon Metabolism Across A Late Pleistocene Permafrost Chronosequence
title_sort life at the frozen limit: microbial carbon metabolism across a late pleistocene permafrost chronosequence
publishDate 2020
url https://doi.org/10.3389/fmicb.2020.01753
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genre permafrost
genre_facet permafrost
op_relation Frontiers in Microbiology--1664-302X
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op_doi https://doi.org/10.3389/fmicb.2020.01753
container_title Frontiers in Microbiology
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