Cargando…
Ambient nitrate switches the ammonium consumption pathway in the euphotic ocean
Phytoplankton assimilation and microbial oxidation of ammonium are two critical conversion pathways in the marine nitrogen cycle. The underlying regulatory mechanisms of these two competing processes remain unclear. Here we show that ambient nitrate acts as a key variable to bifurcate ammonium flow...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834513/ https://www.ncbi.nlm.nih.gov/pubmed/29500422 http://dx.doi.org/10.1038/s41467-018-03363-0 |
_version_ | 1783303659462852608 |
---|---|
author | Wan, Xianhui Sean Sheng, Hua-Xia Dai, Minhan Zhang, Yao Shi, Dalin Trull, Thomas W. Zhu, Yifan Lomas, Michael W. Kao, Shuh-Ji |
author_facet | Wan, Xianhui Sean Sheng, Hua-Xia Dai, Minhan Zhang, Yao Shi, Dalin Trull, Thomas W. Zhu, Yifan Lomas, Michael W. Kao, Shuh-Ji |
author_sort | Wan, Xianhui Sean |
collection | PubMed |
description | Phytoplankton assimilation and microbial oxidation of ammonium are two critical conversion pathways in the marine nitrogen cycle. The underlying regulatory mechanisms of these two competing processes remain unclear. Here we show that ambient nitrate acts as a key variable to bifurcate ammonium flow through assimilation or oxidation, and the depth of the nitracline represents a robust spatial boundary between ammonium assimilators and oxidizers in the stratified ocean. Profiles of ammonium utilization show that phytoplankton assemblages in nitrate-depleted regimes have higher ammonium affinity than nitrifiers. In nitrate replete conditions, by contrast, phytoplankton reduce their ammonium reliance and thus enhance the success of nitrifiers. This finding helps to explain existing discrepancies in the understanding of light inhibition of surface nitrification in the global ocean, and provides further insights into the spatial linkages between oceanic nitrification and new production. |
format | Online Article Text |
id | pubmed-5834513 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58345132018-03-06 Ambient nitrate switches the ammonium consumption pathway in the euphotic ocean Wan, Xianhui Sean Sheng, Hua-Xia Dai, Minhan Zhang, Yao Shi, Dalin Trull, Thomas W. Zhu, Yifan Lomas, Michael W. Kao, Shuh-Ji Nat Commun Article Phytoplankton assimilation and microbial oxidation of ammonium are two critical conversion pathways in the marine nitrogen cycle. The underlying regulatory mechanisms of these two competing processes remain unclear. Here we show that ambient nitrate acts as a key variable to bifurcate ammonium flow through assimilation or oxidation, and the depth of the nitracline represents a robust spatial boundary between ammonium assimilators and oxidizers in the stratified ocean. Profiles of ammonium utilization show that phytoplankton assemblages in nitrate-depleted regimes have higher ammonium affinity than nitrifiers. In nitrate replete conditions, by contrast, phytoplankton reduce their ammonium reliance and thus enhance the success of nitrifiers. This finding helps to explain existing discrepancies in the understanding of light inhibition of surface nitrification in the global ocean, and provides further insights into the spatial linkages between oceanic nitrification and new production. Nature Publishing Group UK 2018-03-02 /pmc/articles/PMC5834513/ /pubmed/29500422 http://dx.doi.org/10.1038/s41467-018-03363-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wan, Xianhui Sean Sheng, Hua-Xia Dai, Minhan Zhang, Yao Shi, Dalin Trull, Thomas W. Zhu, Yifan Lomas, Michael W. Kao, Shuh-Ji Ambient nitrate switches the ammonium consumption pathway in the euphotic ocean |
title | Ambient nitrate switches the ammonium consumption pathway in the euphotic ocean |
title_full | Ambient nitrate switches the ammonium consumption pathway in the euphotic ocean |
title_fullStr | Ambient nitrate switches the ammonium consumption pathway in the euphotic ocean |
title_full_unstemmed | Ambient nitrate switches the ammonium consumption pathway in the euphotic ocean |
title_short | Ambient nitrate switches the ammonium consumption pathway in the euphotic ocean |
title_sort | ambient nitrate switches the ammonium consumption pathway in the euphotic ocean |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834513/ https://www.ncbi.nlm.nih.gov/pubmed/29500422 http://dx.doi.org/10.1038/s41467-018-03363-0 |
work_keys_str_mv | AT wanxianhuisean ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean AT shenghuaxia ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean AT daiminhan ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean AT zhangyao ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean AT shidalin ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean AT trullthomasw ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean AT zhuyifan ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean AT lomasmichaelw ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean AT kaoshuhji ambientnitrateswitchestheammoniumconsumptionpathwayintheeuphoticocean |