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Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with (13)C-Glycine and FACE CO(2)

It is vital to understand responses of soil microorganisms to predicted climate changes, as these directly control soil carbon (C) dynamics. The rate of turnover of soil organic carbon is mediated by soil microorganisms whose activity may be affected by climate change. After one year of multifactori...

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Autores principales: Andresen, Louise C., Dungait, Jennifer A. J., Bol, Roland, Selsted, Merete B., Ambus, Per, Michelsen, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893180/
https://www.ncbi.nlm.nih.gov/pubmed/24454793
http://dx.doi.org/10.1371/journal.pone.0085070
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author Andresen, Louise C.
Dungait, Jennifer A. J.
Bol, Roland
Selsted, Merete B.
Ambus, Per
Michelsen, Anders
author_facet Andresen, Louise C.
Dungait, Jennifer A. J.
Bol, Roland
Selsted, Merete B.
Ambus, Per
Michelsen, Anders
author_sort Andresen, Louise C.
collection PubMed
description It is vital to understand responses of soil microorganisms to predicted climate changes, as these directly control soil carbon (C) dynamics. The rate of turnover of soil organic carbon is mediated by soil microorganisms whose activity may be affected by climate change. After one year of multifactorial climate change treatments, at an undisturbed temperate heathland, soil microbial community dynamics were investigated by injection of a very small concentration (5.12 µg C g(−1) soil) of (13)C-labeled glycine ((13)C(2), 99 atom %) to soils in situ. Plots were treated with elevated temperature (+1°C, T), summer drought (D) and elevated atmospheric carbon dioxide (510 ppm [CO2]), as well as combined treatments (TD, TCO2, DCO2 and TDCO2). The (13)C enrichment of respired CO(2) and of phospholipid fatty acids (PLFAs) was determined after 24 h. (13)C-glycine incorporation into the biomarker PLFAs for specific microbial groups (Gram positive bacteria, Gram negative bacteria, actinobacteria and fungi) was quantified using gas chromatography-combustion-stable isotope ratio mass spectrometry (GC-C-IRMS). Gram positive bacteria opportunistically utilized the freshly added glycine substrate, i.e. incorporated (13)C in all treatments, whereas fungi had minor or no glycine derived (13)C-enrichment, hence slowly reacting to a new substrate. The effects of elevated CO(2) did suggest increased direct incorporation of glycine in microbial biomass, in particular in G(+) bacteria, in an ecosystem subjected to elevated CO(2). Warming decreased the concentration of PLFAs in general. The FACE CO(2) was (13)C-depleted (δ(13)C = 12.2‰) compared to ambient (δ(13)C = ∼−8‰), and this enabled observation of the integrated longer term responses of soil microorganisms to the FACE over one year. All together, the bacterial (and not fungal) utilization of glycine indicates substrate preference and resource partitioning in the microbial community, and therefore suggests a diversified response pattern to future changes in substrate availability and climatic factors.
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spelling pubmed-38931802014-01-21 Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with (13)C-Glycine and FACE CO(2) Andresen, Louise C. Dungait, Jennifer A. J. Bol, Roland Selsted, Merete B. Ambus, Per Michelsen, Anders PLoS One Research Article It is vital to understand responses of soil microorganisms to predicted climate changes, as these directly control soil carbon (C) dynamics. The rate of turnover of soil organic carbon is mediated by soil microorganisms whose activity may be affected by climate change. After one year of multifactorial climate change treatments, at an undisturbed temperate heathland, soil microbial community dynamics were investigated by injection of a very small concentration (5.12 µg C g(−1) soil) of (13)C-labeled glycine ((13)C(2), 99 atom %) to soils in situ. Plots were treated with elevated temperature (+1°C, T), summer drought (D) and elevated atmospheric carbon dioxide (510 ppm [CO2]), as well as combined treatments (TD, TCO2, DCO2 and TDCO2). The (13)C enrichment of respired CO(2) and of phospholipid fatty acids (PLFAs) was determined after 24 h. (13)C-glycine incorporation into the biomarker PLFAs for specific microbial groups (Gram positive bacteria, Gram negative bacteria, actinobacteria and fungi) was quantified using gas chromatography-combustion-stable isotope ratio mass spectrometry (GC-C-IRMS). Gram positive bacteria opportunistically utilized the freshly added glycine substrate, i.e. incorporated (13)C in all treatments, whereas fungi had minor or no glycine derived (13)C-enrichment, hence slowly reacting to a new substrate. The effects of elevated CO(2) did suggest increased direct incorporation of glycine in microbial biomass, in particular in G(+) bacteria, in an ecosystem subjected to elevated CO(2). Warming decreased the concentration of PLFAs in general. The FACE CO(2) was (13)C-depleted (δ(13)C = 12.2‰) compared to ambient (δ(13)C = ∼−8‰), and this enabled observation of the integrated longer term responses of soil microorganisms to the FACE over one year. All together, the bacterial (and not fungal) utilization of glycine indicates substrate preference and resource partitioning in the microbial community, and therefore suggests a diversified response pattern to future changes in substrate availability and climatic factors. Public Library of Science 2014-01-15 /pmc/articles/PMC3893180/ /pubmed/24454793 http://dx.doi.org/10.1371/journal.pone.0085070 Text en © 2014 Andresen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Andresen, Louise C.
Dungait, Jennifer A. J.
Bol, Roland
Selsted, Merete B.
Ambus, Per
Michelsen, Anders
Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with (13)C-Glycine and FACE CO(2)
title Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with (13)C-Glycine and FACE CO(2)
title_full Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with (13)C-Glycine and FACE CO(2)
title_fullStr Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with (13)C-Glycine and FACE CO(2)
title_full_unstemmed Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with (13)C-Glycine and FACE CO(2)
title_short Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with (13)C-Glycine and FACE CO(2)
title_sort bacteria and fungi respond differently to multifactorial climate change in a temperate heathland, traced with (13)c-glycine and face co(2)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3893180/
https://www.ncbi.nlm.nih.gov/pubmed/24454793
http://dx.doi.org/10.1371/journal.pone.0085070
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