Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with .sup.13C-Glycine and FACE CO.sub.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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Published in:PloS one Vol. 9; no. 1; p. e85070
Main Authors: Andresen, Louise C, Dungait, Jennifer A. J, Bol, Roland, Selsted, Merete B, Ambus, Per, Michelsen, Anders
Format: Journal Article
Language:English
Published: Public Library of Science 15-01-2014
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Abstract 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 [micro]g C g.sup.-1 soil) of .sup.13 C-labeled glycine (.sup.13 C.sub.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 .sup.13 C enrichment of respired CO.sub.2 and of phospholipid fatty acids (PLFAs) was determined after 24 h. .sup.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).
AbstractList 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 [micro]g C g.sup.-1 soil) of .sup.13 C-labeled glycine (.sup.13 C.sub.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 .sup.13 C enrichment of respired CO.sub.2 and of phospholipid fatty acids (PLFAs) was determined after 24 h. .sup.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).
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 [micro]g C g.sup.-1 soil) of .sup.13 C-labeled glycine (.sup.13 C.sub.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 .sup.13 C enrichment of respired CO.sub.2 and of phospholipid fatty acids (PLFAs) was determined after 24 h. .sup.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 .sup.13 C in all treatments, whereas fungi had minor or no glycine derived .sup.13 C-enrichment, hence slowly reacting to a new substrate. The effects of elevated CO.sub.2 did suggest increased direct incorporation of glycine in microbial biomass, in particular in G.sup.+ bacteria, in an ecosystem subjected to elevated CO.sub.2 . Warming decreased the concentration of PLFAs in general. The FACE CO.sub.2 was .sup.13 C-depleted ([delta].sup.13 C = 12.2%) compared to ambient ([delta].sup.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.
Audience Academic
Author Ambus, Per
Selsted, Merete B
Michelsen, Anders
Andresen, Louise C
Dungait, Jennifer A. J
Bol, Roland
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  fullname: Michelsen, Anders
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SubjectTerms Atmospheric carbon dioxide
Bacteria
Ecosystems
Fatty acids
Fungi
Global temperature changes
Glycine
Heathlands
Soil carbon
Soil microbiology
Title Bacteria and Fungi Respond Differently to Multifactorial Climate Change in a Temperate Heathland, Traced with .sup.13C-Glycine and FACE CO.sub.2
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