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Combing δ(15)N and δ(18)O to identify the distribution and the potential sources of nitrate in human-impacted watersheds, Shandong, China
Identifying the anthropogenic and natural sources of nitrate emissions contributing to surface water continues to be an enormous challenge. It is necessary to control the water quality in the watershed impacted by human disturbance. In this study, water chemical parameters including nitrate (NO(3)(−...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081639/ https://www.ncbi.nlm.nih.gov/pubmed/35540112 http://dx.doi.org/10.1039/c8ra04364g |
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author | Yang, Baoshan Wang, Hui Jiang, Yingkui Dong, Fang He, Xinhua Lai, Xiaoshuang |
author_facet | Yang, Baoshan Wang, Hui Jiang, Yingkui Dong, Fang He, Xinhua Lai, Xiaoshuang |
author_sort | Yang, Baoshan |
collection | PubMed |
description | Identifying the anthropogenic and natural sources of nitrate emissions contributing to surface water continues to be an enormous challenge. It is necessary to control the water quality in the watershed impacted by human disturbance. In this study, water chemical parameters including nitrate (NO(3)(−)) concentrations, δ(15)N–NO(3)(−), δ(18)O–NO(3)(−), and δ(18)O–H(2)O were analyzed to investigate the contamination and sources of NO(3)(−) in two watershed rivers (Jinyun, JYN and Jinyang, JYA), Jinan, Shandong, China. Results indicated NO(3)(−) concentrations in the JYN were significantly higher than those in the JYA (P < 0.05), probably because of high N input of the extensive farmlands or orchards in the drainage basin. δ(15)N–NO(3)(−) and δ(18)O–NO(3)(−), associated with Cl(−), indicated that nitrate-nitrogen (NO(3)(−)–N) was not derived from atmospheric deposition but came principally from manure/sewage and soil organic matter in these two watersheds. The microbial nitrification took place in the nitrate of manure/sewage and soil nitrate. The combination of NO(3)(−) concentration and nitrogen and oxygen isotope suggested that NO(3)(−) had undergone microbial denitrification after entering the rivers. Furthermore, NO(3)(−) concentrations had significant temporal and spatial variation highlighting differential sources and fates. These results expand our understanding of mechanisms driving NO(3)(−) retention and transport and provide strategies in managing NO(3)(−) contamination in different land use watersheds around the world. |
format | Online Article Text |
id | pubmed-9081639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90816392022-05-09 Combing δ(15)N and δ(18)O to identify the distribution and the potential sources of nitrate in human-impacted watersheds, Shandong, China Yang, Baoshan Wang, Hui Jiang, Yingkui Dong, Fang He, Xinhua Lai, Xiaoshuang RSC Adv Chemistry Identifying the anthropogenic and natural sources of nitrate emissions contributing to surface water continues to be an enormous challenge. It is necessary to control the water quality in the watershed impacted by human disturbance. In this study, water chemical parameters including nitrate (NO(3)(−)) concentrations, δ(15)N–NO(3)(−), δ(18)O–NO(3)(−), and δ(18)O–H(2)O were analyzed to investigate the contamination and sources of NO(3)(−) in two watershed rivers (Jinyun, JYN and Jinyang, JYA), Jinan, Shandong, China. Results indicated NO(3)(−) concentrations in the JYN were significantly higher than those in the JYA (P < 0.05), probably because of high N input of the extensive farmlands or orchards in the drainage basin. δ(15)N–NO(3)(−) and δ(18)O–NO(3)(−), associated with Cl(−), indicated that nitrate-nitrogen (NO(3)(−)–N) was not derived from atmospheric deposition but came principally from manure/sewage and soil organic matter in these two watersheds. The microbial nitrification took place in the nitrate of manure/sewage and soil nitrate. The combination of NO(3)(−) concentration and nitrogen and oxygen isotope suggested that NO(3)(−) had undergone microbial denitrification after entering the rivers. Furthermore, NO(3)(−) concentrations had significant temporal and spatial variation highlighting differential sources and fates. These results expand our understanding of mechanisms driving NO(3)(−) retention and transport and provide strategies in managing NO(3)(−) contamination in different land use watersheds around the world. The Royal Society of Chemistry 2018-06-26 /pmc/articles/PMC9081639/ /pubmed/35540112 http://dx.doi.org/10.1039/c8ra04364g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Yang, Baoshan Wang, Hui Jiang, Yingkui Dong, Fang He, Xinhua Lai, Xiaoshuang Combing δ(15)N and δ(18)O to identify the distribution and the potential sources of nitrate in human-impacted watersheds, Shandong, China |
title | Combing δ(15)N and δ(18)O to identify the distribution and the potential sources of nitrate in human-impacted watersheds, Shandong, China |
title_full | Combing δ(15)N and δ(18)O to identify the distribution and the potential sources of nitrate in human-impacted watersheds, Shandong, China |
title_fullStr | Combing δ(15)N and δ(18)O to identify the distribution and the potential sources of nitrate in human-impacted watersheds, Shandong, China |
title_full_unstemmed | Combing δ(15)N and δ(18)O to identify the distribution and the potential sources of nitrate in human-impacted watersheds, Shandong, China |
title_short | Combing δ(15)N and δ(18)O to identify the distribution and the potential sources of nitrate in human-impacted watersheds, Shandong, China |
title_sort | combing δ(15)n and δ(18)o to identify the distribution and the potential sources of nitrate in human-impacted watersheds, shandong, china |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081639/ https://www.ncbi.nlm.nih.gov/pubmed/35540112 http://dx.doi.org/10.1039/c8ra04364g |
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