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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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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. |
format | Online Article Text |
id | pubmed-6282961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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