First evidence for cold-adapted anaerobic oxidation of methane in deep sediments of thermokarst lakes
Microbial decomposition of thawed permafrost carbon in thermokarst lakes leads to the release of ancient carbon as the greenhouse gas methane (CH4), yet potential mitigating processes are not understood. Here, we report δ13C-CH4 signatures in the pore water of a thermokarst lake sediment core that p...
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Veröffentlicht in: | Environmental Research Communications 2019-04, Vol.1 (2), p.21002 |
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description | Microbial decomposition of thawed permafrost carbon in thermokarst lakes leads to the release of ancient carbon as the greenhouse gas methane (CH4), yet potential mitigating processes are not understood. Here, we report δ13C-CH4 signatures in the pore water of a thermokarst lake sediment core that points towards in situ occurrence of anaerobic oxidation of methane (AOM). Analysis of the microbial communities showed a natural enrichment in CH4-oxidizing archaeal communities that occur in sediment horizons at temperatures near 0 °C. These archaea also showed high rates of AOM in laboratory incubations. Calculation of the stable isotopes suggests that 41 to 83% of in situ dissolved CH4 is consumed anaerobically. Quantification of functional genes (mcrA) for anaerobic methanotrophic communities revealed up to 6.7 0.7 × 105 copy numbers g−1 wet weight and showed similar abundances to bacterial 16S rRNA gene sequences in the sediment layers with the highest AOM rates. We conclude that these AOM communities are fueled by CH4 produced from permafrost organic matter degradation in the underlying sediments that represent the radially expanding permafrost thaw front beneath the lake. If these communities are widespread in thermokarst environments, they could have a major mitigating effect on the global CH4 emissions. |
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Here, we report δ13C-CH4 signatures in the pore water of a thermokarst lake sediment core that points towards in situ occurrence of anaerobic oxidation of methane (AOM). Analysis of the microbial communities showed a natural enrichment in CH4-oxidizing archaeal communities that occur in sediment horizons at temperatures near 0 °C. These archaea also showed high rates of AOM in laboratory incubations. Calculation of the stable isotopes suggests that 41 to 83% of in situ dissolved CH4 is consumed anaerobically. Quantification of functional genes (mcrA) for anaerobic methanotrophic communities revealed up to 6.7 0.7 × 105 copy numbers g−1 wet weight and showed similar abundances to bacterial 16S rRNA gene sequences in the sediment layers with the highest AOM rates. We conclude that these AOM communities are fueled by CH4 produced from permafrost organic matter degradation in the underlying sediments that represent the radially expanding permafrost thaw front beneath the lake. If these communities are widespread in thermokarst environments, they could have a major mitigating effect on the global CH4 emissions.</description><identifier>ISSN: 2515-7620</identifier><identifier>EISSN: 2515-7620</identifier><identifier>DOI: 10.1088/2515-7620/ab1042</identifier><language>eng</language><publisher>Bristol: IOP Publishing</publisher><subject>Anaerobic microorganisms ; ANME-2d ; Archaea ; Biodegradation ; C-methane ; Carbon ; Environmental degradation ; Gene sequencing ; Greenhouse effect ; Greenhouse gases ; Isotopes ; Lake sediments ; Lakes ; Methane ; Microbial activity ; Microorganisms ; Organic matter ; Oxidation ; Permafrost ; Pore water ; rRNA 16S ; Sediments ; Stable isotopes ; subsurface</subject><ispartof>Environmental Research Communications, 2019-04, Vol.1 (2), p.21002</ispartof><rights>2019 The Author(s). Published by IOP Publishing Ltd</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). 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Res. Commun</addtitle><description>Microbial decomposition of thawed permafrost carbon in thermokarst lakes leads to the release of ancient carbon as the greenhouse gas methane (CH4), yet potential mitigating processes are not understood. Here, we report δ13C-CH4 signatures in the pore water of a thermokarst lake sediment core that points towards in situ occurrence of anaerobic oxidation of methane (AOM). Analysis of the microbial communities showed a natural enrichment in CH4-oxidizing archaeal communities that occur in sediment horizons at temperatures near 0 °C. These archaea also showed high rates of AOM in laboratory incubations. Calculation of the stable isotopes suggests that 41 to 83% of in situ dissolved CH4 is consumed anaerobically. Quantification of functional genes (mcrA) for anaerobic methanotrophic communities revealed up to 6.7 0.7 × 105 copy numbers g−1 wet weight and showed similar abundances to bacterial 16S rRNA gene sequences in the sediment layers with the highest AOM rates. We conclude that these AOM communities are fueled by CH4 produced from permafrost organic matter degradation in the underlying sediments that represent the radially expanding permafrost thaw front beneath the lake. 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Res. Commun</addtitle><date>2019-04-03</date><risdate>2019</risdate><volume>1</volume><issue>2</issue><spage>21002</spage><pages>21002-</pages><issn>2515-7620</issn><eissn>2515-7620</eissn><abstract>Microbial decomposition of thawed permafrost carbon in thermokarst lakes leads to the release of ancient carbon as the greenhouse gas methane (CH4), yet potential mitigating processes are not understood. Here, we report δ13C-CH4 signatures in the pore water of a thermokarst lake sediment core that points towards in situ occurrence of anaerobic oxidation of methane (AOM). Analysis of the microbial communities showed a natural enrichment in CH4-oxidizing archaeal communities that occur in sediment horizons at temperatures near 0 °C. These archaea also showed high rates of AOM in laboratory incubations. Calculation of the stable isotopes suggests that 41 to 83% of in situ dissolved CH4 is consumed anaerobically. Quantification of functional genes (mcrA) for anaerobic methanotrophic communities revealed up to 6.7 0.7 × 105 copy numbers g−1 wet weight and showed similar abundances to bacterial 16S rRNA gene sequences in the sediment layers with the highest AOM rates. We conclude that these AOM communities are fueled by CH4 produced from permafrost organic matter degradation in the underlying sediments that represent the radially expanding permafrost thaw front beneath the lake. If these communities are widespread in thermokarst environments, they could have a major mitigating effect on the global CH4 emissions.</abstract><cop>Bristol</cop><pub>IOP Publishing</pub><doi>10.1088/2515-7620/ab1042</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9365-0616</orcidid><orcidid>https://orcid.org/0000-0001-7777-4520</orcidid><orcidid>https://orcid.org/0000-0002-9389-7093</orcidid><orcidid>https://orcid.org/0000-0003-2079-2896</orcidid><orcidid>https://orcid.org/0000-0002-8243-4456</orcidid><orcidid>https://orcid.org/0000-0001-7263-8917</orcidid><orcidid>https://orcid.org/0000-0003-3692-0952</orcidid><orcidid>https://orcid.org/0000-0002-4070-3400</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anaerobic microorganisms ANME-2d Archaea Biodegradation C-methane Carbon Environmental degradation Gene sequencing Greenhouse effect Greenhouse gases Isotopes Lake sediments Lakes Methane Microbial activity Microorganisms Organic matter Oxidation Permafrost Pore water rRNA 16S Sediments Stable isotopes subsurface |
title | First evidence for cold-adapted anaerobic oxidation of methane in deep sediments of thermokarst lakes |
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