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Evidence for fungal and chemodenitrification based N(2)O flux from nitrogen impacted coastal sediments
Although increasing atmospheric nitrous oxide (N(2)O) has been linked to nitrogen loading, predicting emissions remains difficult, in part due to challenges in disentangling diverse N(2)O production pathways. As coastal ecosystems are especially impacted by elevated nitrogen, we investigated control...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465357/ https://www.ncbi.nlm.nih.gov/pubmed/28580932 http://dx.doi.org/10.1038/ncomms15595 |
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author | Wankel, Scott D. Ziebis, Wiebke Buchwald, Carolyn Charoenpong, Chawalit de Beer, Dirk Dentinger, Jane Xu, Zhenjiang Zengler, Karsten |
author_facet | Wankel, Scott D. Ziebis, Wiebke Buchwald, Carolyn Charoenpong, Chawalit de Beer, Dirk Dentinger, Jane Xu, Zhenjiang Zengler, Karsten |
author_sort | Wankel, Scott D. |
collection | PubMed |
description | Although increasing atmospheric nitrous oxide (N(2)O) has been linked to nitrogen loading, predicting emissions remains difficult, in part due to challenges in disentangling diverse N(2)O production pathways. As coastal ecosystems are especially impacted by elevated nitrogen, we investigated controls on N(2)O production mechanisms in intertidal sediments using novel isotopic approaches and microsensors in flow-through incubations. Here we show that during incubations with elevated nitrate, increased N(2)O fluxes are not mediated by direct bacterial activity, but instead are largely catalysed by fungal denitrification and/or abiotic reactions (e.g., chemodenitrification). Results of these incubations shed new light on nitrogen cycling complexity and possible factors underlying variability of N(2)O fluxes, driven in part by fungal respiration and/or iron redox cycling. As both processes exhibit N(2)O yields typically far greater than direct bacterial production, these results emphasize their possibly substantial, yet widely overlooked, role in N(2)O fluxes, especially in redox-dynamic sediments of coastal ecosystems. |
format | Online Article Text |
id | pubmed-5465357 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54653572017-06-22 Evidence for fungal and chemodenitrification based N(2)O flux from nitrogen impacted coastal sediments Wankel, Scott D. Ziebis, Wiebke Buchwald, Carolyn Charoenpong, Chawalit de Beer, Dirk Dentinger, Jane Xu, Zhenjiang Zengler, Karsten Nat Commun Article Although increasing atmospheric nitrous oxide (N(2)O) has been linked to nitrogen loading, predicting emissions remains difficult, in part due to challenges in disentangling diverse N(2)O production pathways. As coastal ecosystems are especially impacted by elevated nitrogen, we investigated controls on N(2)O production mechanisms in intertidal sediments using novel isotopic approaches and microsensors in flow-through incubations. Here we show that during incubations with elevated nitrate, increased N(2)O fluxes are not mediated by direct bacterial activity, but instead are largely catalysed by fungal denitrification and/or abiotic reactions (e.g., chemodenitrification). Results of these incubations shed new light on nitrogen cycling complexity and possible factors underlying variability of N(2)O fluxes, driven in part by fungal respiration and/or iron redox cycling. As both processes exhibit N(2)O yields typically far greater than direct bacterial production, these results emphasize their possibly substantial, yet widely overlooked, role in N(2)O fluxes, especially in redox-dynamic sediments of coastal ecosystems. Nature Publishing Group 2017-06-05 /pmc/articles/PMC5465357/ /pubmed/28580932 http://dx.doi.org/10.1038/ncomms15595 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wankel, Scott D. Ziebis, Wiebke Buchwald, Carolyn Charoenpong, Chawalit de Beer, Dirk Dentinger, Jane Xu, Zhenjiang Zengler, Karsten Evidence for fungal and chemodenitrification based N(2)O flux from nitrogen impacted coastal sediments |
title | Evidence for fungal and chemodenitrification based N(2)O flux from nitrogen impacted coastal sediments |
title_full | Evidence for fungal and chemodenitrification based N(2)O flux from nitrogen impacted coastal sediments |
title_fullStr | Evidence for fungal and chemodenitrification based N(2)O flux from nitrogen impacted coastal sediments |
title_full_unstemmed | Evidence for fungal and chemodenitrification based N(2)O flux from nitrogen impacted coastal sediments |
title_short | Evidence for fungal and chemodenitrification based N(2)O flux from nitrogen impacted coastal sediments |
title_sort | evidence for fungal and chemodenitrification based n(2)o flux from nitrogen impacted coastal sediments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5465357/ https://www.ncbi.nlm.nih.gov/pubmed/28580932 http://dx.doi.org/10.1038/ncomms15595 |
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