Details
Originalsprache | Englisch |
---|---|
Aufsatznummer | 1976 |
Fachzeitschrift | Frontiers in microbiology |
Jahrgang | 8 |
Ausgabenummer | 8 |
Publikationsstatus | Veröffentlicht - 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
- Immunologie und Mikrobiologie (insg.)
- Mikrobiologie
- Medizin (insg.)
- Mikrobiologie (medizinisch)
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in: Frontiers in microbiology, Jahrgang 8, Nr. 8, 1976, 18.10.2017.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
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
UR - http://www.scopus.com/inward/record.url?scp=85031741876&partnerID=8YFLogxK
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 -