Soil Conditions Rather Than Long-Term Exposure to Elevated CO2 Affect Soil Microbial Communities Associated with N-Cycling.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Autoren

  • Kristof Brenzinger
  • Katharina Kujala
  • Marcus A. Horn
  • Gerald Moser
  • Cécile Guillet
  • Claudia Kammann
  • Christoph Müller
  • Gesche Braker

Organisationseinheiten

Externe Organisationen

  • Max-Planck-Institut für terrestrische Mikrobiologie
  • Justus-Liebig-Universität Gießen
  • University of Oulu
  • Universität Bayreuth
  • Hochschule Geisenheim University
  • University College Dublin
  • Christian-Albrechts-Universität zu Kiel (CAU)
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Aufsatznummer1976
FachzeitschriftFrontiers in microbiology
Jahrgang8
Ausgabenummer8
PublikationsstatusVeröffentlicht - 18 Okt. 2017

Abstract

Continuously rising atmospheric CO 2 concentrations may lead to an increased transfer of organic C from plants to the soil through rhizodeposition and may affect the interaction between the C- and N-cycle. For instance, fumigation of soils with elevated CO 2 (eCO 2) concentrations (20% higher compared to current atmospheric concentrations) at the Giessen Free-Air Carbon Dioxide Enrichment (GiFACE) sites resulted in a more than 2-fold increase of long-term N 2O emissions and an increase in dissimilatory reduction of nitrate compared to ambient CO 2 (aCO 2). We hypothesized that the observed differences in soil functioning were based on differences in the abundance and composition of microbial communities in general and especially of those which are responsible for N-transformations in soil. We also expected eCO 2 effects on soil parameters, such as on nitrate as previously reported. To explore the impact of long-term eCO 2 on soil microbial communities, we applied a molecular approach (qPCR, T-RFLP, and 454 pyrosequencing). Microbial groups were analyzed in soil of three sets of two FACE plots (three replicate samples from each plot), which were fumigated with eCO 2 and aCO 2, respectively. N-fixers, denitrifiers, archaeal and bacterial ammonia oxidizers, and dissimilatory nitrate reducers producing ammonia were targeted by analysis of functional marker genes, and the overall archaeal community by 16S rRNA genes. Remarkably, soil parameters as well as the abundance and composition of microbial communities in the top soil under eCO 2 differed only slightly from soil under aCO 2. Wherever differences in microbial community abundance and composition were detected, they were not linked to CO 2 level but rather determined by differences in soil parameters (e.g., soil moisture content) due to the localization of the GiFACE sets in the experimental field. We concluded that +20% eCO 2 had little to no effect on the overall microbial community involved in N-cycling in the soil but that spatial heterogeneity over extended periods had shaped microbial communities at particular sites in the field. Hence, microbial community composition and abundance alone cannot explain the functional differences leading to higher N 2O emissions under eCO 2 and future studies should aim at exploring the active members of the soil microbial community.

ASJC Scopus Sachgebiete

Zitieren

Soil Conditions Rather Than Long-Term Exposure to Elevated CO2 Affect Soil Microbial Communities Associated with N-Cycling. / Brenzinger, Kristof; Kujala, Katharina; Horn, Marcus A. et al.
in: Frontiers in microbiology, Jahrgang 8, Nr. 8, 1976, 18.10.2017.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Brenzinger K, Kujala K, Horn MA, Moser G, Guillet C, Kammann C et al. Soil Conditions Rather Than Long-Term Exposure to Elevated CO2 Affect Soil Microbial Communities Associated with N-Cycling. Frontiers in microbiology. 2017 Okt 18;8(8):1976. doi: 10.3389/fmicb.2017.01976, 10.15488/2281
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title = "Soil Conditions Rather Than Long-Term Exposure to Elevated CO2 Affect Soil Microbial Communities Associated with N-Cycling.",
abstract = "Continuously rising atmospheric CO 2 concentrations may lead to an increased transfer of organic C from plants to the soil through rhizodeposition and may affect the interaction between the C- and N-cycle. For instance, fumigation of soils with elevated CO 2 (eCO 2) concentrations (20% higher compared to current atmospheric concentrations) at the Giessen Free-Air Carbon Dioxide Enrichment (GiFACE) sites resulted in a more than 2-fold increase of long-term N 2O emissions and an increase in dissimilatory reduction of nitrate compared to ambient CO 2 (aCO 2). We hypothesized that the observed differences in soil functioning were based on differences in the abundance and composition of microbial communities in general and especially of those which are responsible for N-transformations in soil. We also expected eCO 2 effects on soil parameters, such as on nitrate as previously reported. To explore the impact of long-term eCO 2 on soil microbial communities, we applied a molecular approach (qPCR, T-RFLP, and 454 pyrosequencing). Microbial groups were analyzed in soil of three sets of two FACE plots (three replicate samples from each plot), which were fumigated with eCO 2 and aCO 2, respectively. N-fixers, denitrifiers, archaeal and bacterial ammonia oxidizers, and dissimilatory nitrate reducers producing ammonia were targeted by analysis of functional marker genes, and the overall archaeal community by 16S rRNA genes. Remarkably, soil parameters as well as the abundance and composition of microbial communities in the top soil under eCO 2 differed only slightly from soil under aCO 2. Wherever differences in microbial community abundance and composition were detected, they were not linked to CO 2 level but rather determined by differences in soil parameters (e.g., soil moisture content) due to the localization of the GiFACE sets in the experimental field. We concluded that +20% eCO 2 had little to no effect on the overall microbial community involved in N-cycling in the soil but that spatial heterogeneity over extended periods had shaped microbial communities at particular sites in the field. Hence, microbial community composition and abundance alone cannot explain the functional differences leading to higher N 2O emissions under eCO 2 and future studies should aim at exploring the active members of the soil microbial community. ",
keywords = "Ammonia oxidizers, DNRA, Denitrifiers, Elevated CO, FACE, N O, N-fixers",
author = "Kristof Brenzinger and Katharina Kujala and Horn, {Marcus A.} and Gerald Moser and C{\'e}cile Guillet and Claudia Kammann and Christoph M{\"u}ller and Gesche Braker",
note = "Publisher Copyright: {\textcopyright} 2017 Brenzinger, Kujala, Horn, Moser, Guillet, Kammann, M{\"u}ller and Braker. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.",
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Download

TY - JOUR

T1 - Soil Conditions Rather Than Long-Term Exposure to Elevated CO2 Affect Soil Microbial Communities Associated with N-Cycling.

AU - Brenzinger, Kristof

AU - Kujala, Katharina

AU - Horn, Marcus A.

AU - Moser, Gerald

AU - Guillet, Cécile

AU - Kammann, Claudia

AU - Müller, Christoph

AU - Braker, Gesche

N1 - Publisher Copyright: © 2017 Brenzinger, Kujala, Horn, Moser, Guillet, Kammann, Müller and Braker. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.

PY - 2017/10/18

Y1 - 2017/10/18

N2 - Continuously rising atmospheric CO 2 concentrations may lead to an increased transfer of organic C from plants to the soil through rhizodeposition and may affect the interaction between the C- and N-cycle. For instance, fumigation of soils with elevated CO 2 (eCO 2) concentrations (20% higher compared to current atmospheric concentrations) at the Giessen Free-Air Carbon Dioxide Enrichment (GiFACE) sites resulted in a more than 2-fold increase of long-term N 2O emissions and an increase in dissimilatory reduction of nitrate compared to ambient CO 2 (aCO 2). We hypothesized that the observed differences in soil functioning were based on differences in the abundance and composition of microbial communities in general and especially of those which are responsible for N-transformations in soil. We also expected eCO 2 effects on soil parameters, such as on nitrate as previously reported. To explore the impact of long-term eCO 2 on soil microbial communities, we applied a molecular approach (qPCR, T-RFLP, and 454 pyrosequencing). Microbial groups were analyzed in soil of three sets of two FACE plots (three replicate samples from each plot), which were fumigated with eCO 2 and aCO 2, respectively. N-fixers, denitrifiers, archaeal and bacterial ammonia oxidizers, and dissimilatory nitrate reducers producing ammonia were targeted by analysis of functional marker genes, and the overall archaeal community by 16S rRNA genes. Remarkably, soil parameters as well as the abundance and composition of microbial communities in the top soil under eCO 2 differed only slightly from soil under aCO 2. Wherever differences in microbial community abundance and composition were detected, they were not linked to CO 2 level but rather determined by differences in soil parameters (e.g., soil moisture content) due to the localization of the GiFACE sets in the experimental field. We concluded that +20% eCO 2 had little to no effect on the overall microbial community involved in N-cycling in the soil but that spatial heterogeneity over extended periods had shaped microbial communities at particular sites in the field. Hence, microbial community composition and abundance alone cannot explain the functional differences leading to higher N 2O emissions under eCO 2 and future studies should aim at exploring the active members of the soil microbial community.

AB - Continuously rising atmospheric CO 2 concentrations may lead to an increased transfer of organic C from plants to the soil through rhizodeposition and may affect the interaction between the C- and N-cycle. For instance, fumigation of soils with elevated CO 2 (eCO 2) concentrations (20% higher compared to current atmospheric concentrations) at the Giessen Free-Air Carbon Dioxide Enrichment (GiFACE) sites resulted in a more than 2-fold increase of long-term N 2O emissions and an increase in dissimilatory reduction of nitrate compared to ambient CO 2 (aCO 2). We hypothesized that the observed differences in soil functioning were based on differences in the abundance and composition of microbial communities in general and especially of those which are responsible for N-transformations in soil. We also expected eCO 2 effects on soil parameters, such as on nitrate as previously reported. To explore the impact of long-term eCO 2 on soil microbial communities, we applied a molecular approach (qPCR, T-RFLP, and 454 pyrosequencing). Microbial groups were analyzed in soil of three sets of two FACE plots (three replicate samples from each plot), which were fumigated with eCO 2 and aCO 2, respectively. N-fixers, denitrifiers, archaeal and bacterial ammonia oxidizers, and dissimilatory nitrate reducers producing ammonia were targeted by analysis of functional marker genes, and the overall archaeal community by 16S rRNA genes. Remarkably, soil parameters as well as the abundance and composition of microbial communities in the top soil under eCO 2 differed only slightly from soil under aCO 2. Wherever differences in microbial community abundance and composition were detected, they were not linked to CO 2 level but rather determined by differences in soil parameters (e.g., soil moisture content) due to the localization of the GiFACE sets in the experimental field. We concluded that +20% eCO 2 had little to no effect on the overall microbial community involved in N-cycling in the soil but that spatial heterogeneity over extended periods had shaped microbial communities at particular sites in the field. Hence, microbial community composition and abundance alone cannot explain the functional differences leading to higher N 2O emissions under eCO 2 and future studies should aim at exploring the active members of the soil microbial community.

KW - Ammonia oxidizers

KW - DNRA

KW - Denitrifiers

KW - Elevated CO

KW - FACE

KW - N O

KW - N-fixers

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U2 - 10.3389/fmicb.2017.01976

DO - 10.3389/fmicb.2017.01976

M3 - Article

C2 - 29093701

VL - 8

JO - Frontiers in microbiology

JF - Frontiers in microbiology

SN - 1664-302X

IS - 8

M1 - 1976

ER -

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