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A Microbial Link between Elevated CO(2) and Methane Emissions that is Plant Species-Specific

Rising atmospheric CO(2) levels alter the physiology of many plant species, but little is known of changes to root dynamics that may impact soil microbial mediation of greenhouse gas emissions from wetlands. We grew co-occurring wetland plant species that included an invasive reed canary grass (Phal...

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Autores principales: Kao-Kniffin, Jenny, Zhu, Biao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776251/
https://www.ncbi.nlm.nih.gov/pubmed/23784452
http://dx.doi.org/10.1007/s00248-013-0254-8
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author Kao-Kniffin, Jenny
Zhu, Biao
author_facet Kao-Kniffin, Jenny
Zhu, Biao
author_sort Kao-Kniffin, Jenny
collection PubMed
description Rising atmospheric CO(2) levels alter the physiology of many plant species, but little is known of changes to root dynamics that may impact soil microbial mediation of greenhouse gas emissions from wetlands. We grew co-occurring wetland plant species that included an invasive reed canary grass (Phalaris arundinacea L.) and a native woolgrass (Scirpus cyperinus L.) in a controlled greenhouse facility under ambient (380 ppm) and elevated atmospheric CO(2) (700 ppm). We hypothesized that elevated atmospheric CO(2) would increase the abundance of both archaeal methanogen and bacterial methanotroph populations through stimulation of plant root and shoot biomass. We found that methane levels emitted from S. cyperinus shoots increased 1.5-fold under elevated CO(2), while no changes in methane levels were detected from P. arundincea. The increase in methane emissions was not explained by enhanced root or shoot growth of S. cyperinus. Principal components analysis of the total phospholipid fatty acid (PLFA) recovered from microbial cell membranes revealed that elevated CO(2) levels shifted the composition of the microbial community under S. cyperinus, while no changes were detected under P. arundinacea. More detailed analysis of microbial abundance showed no impact of elevated CO(2) on a fatty acid indicative of methanotrophic bacteria (18:2ω6c), and no changes were detected in the terminal restriction fragment length polymorphism (T-RFLP) relative abundance profiles of acetate-utilizing archaeal methanogens. Plant carbon depleted in (13)C was traced into the PLFAs of soil microorganisms as a measure of the plant contribution to microbial PLFA. The relative contribution of plant-derived carbon to PLFA carbon was larger in S. cyperinus compared with P. arundinacea in four PLFAs (i14:0, i15:0, a15:0, and 18:1ω9t). The δ(13)C isotopic values indicate that the contribution of plant-derived carbon to microbial lipids could differ in rhizospheres of CO(2)-responsive plant species, such as S. cyperinus in this study. The results from this study show that the CO(2)–methane link found in S. cyperinus can occur without a corresponding change in methanogen and methanotroph relative abundances, but PLFA analysis indicated shifts in the community profile of bacteria and fungi that were unique to rhizospheres under elevated CO(2).
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spelling pubmed-37762512013-09-20 A Microbial Link between Elevated CO(2) and Methane Emissions that is Plant Species-Specific Kao-Kniffin, Jenny Zhu, Biao Microb Ecol Soil Microbiology Rising atmospheric CO(2) levels alter the physiology of many plant species, but little is known of changes to root dynamics that may impact soil microbial mediation of greenhouse gas emissions from wetlands. We grew co-occurring wetland plant species that included an invasive reed canary grass (Phalaris arundinacea L.) and a native woolgrass (Scirpus cyperinus L.) in a controlled greenhouse facility under ambient (380 ppm) and elevated atmospheric CO(2) (700 ppm). We hypothesized that elevated atmospheric CO(2) would increase the abundance of both archaeal methanogen and bacterial methanotroph populations through stimulation of plant root and shoot biomass. We found that methane levels emitted from S. cyperinus shoots increased 1.5-fold under elevated CO(2), while no changes in methane levels were detected from P. arundincea. The increase in methane emissions was not explained by enhanced root or shoot growth of S. cyperinus. Principal components analysis of the total phospholipid fatty acid (PLFA) recovered from microbial cell membranes revealed that elevated CO(2) levels shifted the composition of the microbial community under S. cyperinus, while no changes were detected under P. arundinacea. More detailed analysis of microbial abundance showed no impact of elevated CO(2) on a fatty acid indicative of methanotrophic bacteria (18:2ω6c), and no changes were detected in the terminal restriction fragment length polymorphism (T-RFLP) relative abundance profiles of acetate-utilizing archaeal methanogens. Plant carbon depleted in (13)C was traced into the PLFAs of soil microorganisms as a measure of the plant contribution to microbial PLFA. The relative contribution of plant-derived carbon to PLFA carbon was larger in S. cyperinus compared with P. arundinacea in four PLFAs (i14:0, i15:0, a15:0, and 18:1ω9t). The δ(13)C isotopic values indicate that the contribution of plant-derived carbon to microbial lipids could differ in rhizospheres of CO(2)-responsive plant species, such as S. cyperinus in this study. The results from this study show that the CO(2)–methane link found in S. cyperinus can occur without a corresponding change in methanogen and methanotroph relative abundances, but PLFA analysis indicated shifts in the community profile of bacteria and fungi that were unique to rhizospheres under elevated CO(2). Springer US 2013-06-20 2013 /pmc/articles/PMC3776251/ /pubmed/23784452 http://dx.doi.org/10.1007/s00248-013-0254-8 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Soil Microbiology
Kao-Kniffin, Jenny
Zhu, Biao
A Microbial Link between Elevated CO(2) and Methane Emissions that is Plant Species-Specific
title A Microbial Link between Elevated CO(2) and Methane Emissions that is Plant Species-Specific
title_full A Microbial Link between Elevated CO(2) and Methane Emissions that is Plant Species-Specific
title_fullStr A Microbial Link between Elevated CO(2) and Methane Emissions that is Plant Species-Specific
title_full_unstemmed A Microbial Link between Elevated CO(2) and Methane Emissions that is Plant Species-Specific
title_short A Microbial Link between Elevated CO(2) and Methane Emissions that is Plant Species-Specific
title_sort microbial link between elevated co(2) and methane emissions that is plant species-specific
topic Soil Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3776251/
https://www.ncbi.nlm.nih.gov/pubmed/23784452
http://dx.doi.org/10.1007/s00248-013-0254-8
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