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Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N(2)O hotspots

Nitrous oxide (N(2)O) is a potent, globally important, greenhouse gas, predominantly released from agricultural soils during nitrogen (N) cycling. Arbuscular mycorrhizal fungi (AMF) form a mutualistic symbiosis with two‐thirds of land plants, providing phosphorus and/or N in exchange for carbon. As...

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Autores principales: Storer, Kate, Coggan, Aisha, Ineson, Phil, Hodge, Angela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282961/
https://www.ncbi.nlm.nih.gov/pubmed/29206293
http://dx.doi.org/10.1111/nph.14931
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author Storer, Kate
Coggan, Aisha
Ineson, Phil
Hodge, Angela
author_facet Storer, Kate
Coggan, Aisha
Ineson, Phil
Hodge, Angela
author_sort Storer, Kate
collection PubMed
description Nitrous oxide (N(2)O) is a potent, globally important, greenhouse gas, predominantly released from agricultural soils during nitrogen (N) cycling. Arbuscular mycorrhizal fungi (AMF) form a mutualistic symbiosis with two‐thirds of land plants, providing phosphorus and/or N in exchange for carbon. As AMF acquire N, it was hypothesized that AMF hyphae may reduce N(2)O production. AMF hyphae were either allowed (AMF) or prevented (nonAMF) access to a compartment containing an organic matter and soil patch in two independent microcosm experiments. Compartment and patch N(2)O production was measured both before and after addition of ammonium and nitrate. In both experiments, N(2)O production decreased when AMF hyphae were present before inorganic N addition. In the presence of AMF hyphae, N(2)O production remained low following ammonium application, but increased in the nonAMF controls. By contrast, negligible N(2)O was produced following nitrate application to either AMF treatment. Thus, the main N(2)O source in this system appeared to be via nitrification, and the production of N(2)O was reduced in the presence of AMF hyphae. It is hypothesized that AMF hyphae may be outcompeting slow‐growing nitrifiers for ammonium. This has significant global implications for our understanding of soil N cycling pathways and N(2)O production.
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spelling pubmed-62829612018-12-14 Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N(2)O hotspots Storer, Kate Coggan, Aisha Ineson, Phil Hodge, Angela New Phytol Research Nitrous oxide (N(2)O) is a potent, globally important, greenhouse gas, predominantly released from agricultural soils during nitrogen (N) cycling. Arbuscular mycorrhizal fungi (AMF) form a mutualistic symbiosis with two‐thirds of land plants, providing phosphorus and/or N in exchange for carbon. As AMF acquire N, it was hypothesized that AMF hyphae may reduce N(2)O production. AMF hyphae were either allowed (AMF) or prevented (nonAMF) access to a compartment containing an organic matter and soil patch in two independent microcosm experiments. Compartment and patch N(2)O production was measured both before and after addition of ammonium and nitrate. In both experiments, N(2)O production decreased when AMF hyphae were present before inorganic N addition. In the presence of AMF hyphae, N(2)O production remained low following ammonium application, but increased in the nonAMF controls. By contrast, negligible N(2)O was produced following nitrate application to either AMF treatment. Thus, the main N(2)O source in this system appeared to be via nitrification, and the production of N(2)O was reduced in the presence of AMF hyphae. It is hypothesized that AMF hyphae may be outcompeting slow‐growing nitrifiers for ammonium. This has significant global implications for our understanding of soil N cycling pathways and N(2)O production. John Wiley and Sons Inc. 2017-12-05 2018-12 /pmc/articles/PMC6282961/ /pubmed/29206293 http://dx.doi.org/10.1111/nph.14931 Text en © 2017 The Authors. New Phytologist © 2017 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Storer, Kate
Coggan, Aisha
Ineson, Phil
Hodge, Angela
Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N(2)O hotspots
title Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N(2)O hotspots
title_full Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N(2)O hotspots
title_fullStr Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N(2)O hotspots
title_full_unstemmed Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N(2)O hotspots
title_short Arbuscular mycorrhizal fungi reduce nitrous oxide emissions from N(2)O hotspots
title_sort arbuscular mycorrhizal fungi reduce nitrous oxide emissions from n(2)o hotspots
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6282961/
https://www.ncbi.nlm.nih.gov/pubmed/29206293
http://dx.doi.org/10.1111/nph.14931
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