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Seasonal and ecohydrological regulation of active microbial populations involved in DOC, CO(2), and CH(4) fluxes in temperate rainforest soil
The Pacific coastal temperate rainforest (PCTR) is a global hot-spot for carbon cycling and export. Yet the influence of microorganisms on carbon cycling processes in PCTR soil is poorly characterized. We developed and tested a conceptual model of seasonal microbial carbon cycling in PCTR soil throu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461783/ https://www.ncbi.nlm.nih.gov/pubmed/30538276 http://dx.doi.org/10.1038/s41396-018-0334-3 |
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author | Levy-Booth, David J. Giesbrecht, Ian J. W. Kellogg, Colleen T. E. Heger, Thierry J. D’Amore, David V. Keeling, Patrick J. Hallam, Steven J. Mohn, William W. |
author_facet | Levy-Booth, David J. Giesbrecht, Ian J. W. Kellogg, Colleen T. E. Heger, Thierry J. D’Amore, David V. Keeling, Patrick J. Hallam, Steven J. Mohn, William W. |
author_sort | Levy-Booth, David J. |
collection | PubMed |
description | The Pacific coastal temperate rainforest (PCTR) is a global hot-spot for carbon cycling and export. Yet the influence of microorganisms on carbon cycling processes in PCTR soil is poorly characterized. We developed and tested a conceptual model of seasonal microbial carbon cycling in PCTR soil through integration of geochemistry, micro-meteorology, and eukaryotic and prokaryotic ribosomal amplicon (rRNA) sequencing from 216 soil DNA and RNA libraries. Soil moisture and pH increased during the wet season, with significant correlation to net CO(2) flux in peat bog and net CH(4) flux in bog forest soil. Fungal succession in these sites was characterized by the apparent turnover of Archaeorhizomycetes phylotypes accounting for 41% of ITS libraries. Anaerobic prokaryotes, including Syntrophobacteraceae and Methanomicrobia increased in rRNA libraries during the wet season. Putatively active populations of these phylotypes and their biogeochemical marker genes for sulfate and CH(4) cycling, respectively, were positively correlated following rRNA and metatranscriptomic network analysis. The latter phylotype was positively correlated to CH(4) fluxes (r = 0.46, p < 0.0001). Phylotype functional assignments were supported by metatranscriptomic analysis. We propose that active microbial populations respond primarily to changes in hydrology, pH, and nutrient availability. The increased microbial carbon export observed over winter may have ramifications for climate–soil feedbacks in the PCTR. |
format | Online Article Text |
id | pubmed-6461783 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64617832019-06-25 Seasonal and ecohydrological regulation of active microbial populations involved in DOC, CO(2), and CH(4) fluxes in temperate rainforest soil Levy-Booth, David J. Giesbrecht, Ian J. W. Kellogg, Colleen T. E. Heger, Thierry J. D’Amore, David V. Keeling, Patrick J. Hallam, Steven J. Mohn, William W. ISME J Article The Pacific coastal temperate rainforest (PCTR) is a global hot-spot for carbon cycling and export. Yet the influence of microorganisms on carbon cycling processes in PCTR soil is poorly characterized. We developed and tested a conceptual model of seasonal microbial carbon cycling in PCTR soil through integration of geochemistry, micro-meteorology, and eukaryotic and prokaryotic ribosomal amplicon (rRNA) sequencing from 216 soil DNA and RNA libraries. Soil moisture and pH increased during the wet season, with significant correlation to net CO(2) flux in peat bog and net CH(4) flux in bog forest soil. Fungal succession in these sites was characterized by the apparent turnover of Archaeorhizomycetes phylotypes accounting for 41% of ITS libraries. Anaerobic prokaryotes, including Syntrophobacteraceae and Methanomicrobia increased in rRNA libraries during the wet season. Putatively active populations of these phylotypes and their biogeochemical marker genes for sulfate and CH(4) cycling, respectively, were positively correlated following rRNA and metatranscriptomic network analysis. The latter phylotype was positively correlated to CH(4) fluxes (r = 0.46, p < 0.0001). Phylotype functional assignments were supported by metatranscriptomic analysis. We propose that active microbial populations respond primarily to changes in hydrology, pH, and nutrient availability. The increased microbial carbon export observed over winter may have ramifications for climate–soil feedbacks in the PCTR. Nature Publishing Group UK 2018-12-11 2019-04 /pmc/articles/PMC6461783/ /pubmed/30538276 http://dx.doi.org/10.1038/s41396-018-0334-3 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Levy-Booth, David J. Giesbrecht, Ian J. W. Kellogg, Colleen T. E. Heger, Thierry J. D’Amore, David V. Keeling, Patrick J. Hallam, Steven J. Mohn, William W. Seasonal and ecohydrological regulation of active microbial populations involved in DOC, CO(2), and CH(4) fluxes in temperate rainforest soil |
title | Seasonal and ecohydrological regulation of active microbial populations involved in DOC, CO(2), and CH(4) fluxes in temperate rainforest soil |
title_full | Seasonal and ecohydrological regulation of active microbial populations involved in DOC, CO(2), and CH(4) fluxes in temperate rainforest soil |
title_fullStr | Seasonal and ecohydrological regulation of active microbial populations involved in DOC, CO(2), and CH(4) fluxes in temperate rainforest soil |
title_full_unstemmed | Seasonal and ecohydrological regulation of active microbial populations involved in DOC, CO(2), and CH(4) fluxes in temperate rainforest soil |
title_short | Seasonal and ecohydrological regulation of active microbial populations involved in DOC, CO(2), and CH(4) fluxes in temperate rainforest soil |
title_sort | seasonal and ecohydrological regulation of active microbial populations involved in doc, co(2), and ch(4) fluxes in temperate rainforest soil |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461783/ https://www.ncbi.nlm.nih.gov/pubmed/30538276 http://dx.doi.org/10.1038/s41396-018-0334-3 |
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