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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)(−...

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Detalles Bibliográficos
Autores principales: Yang, Baoshan, Wang, Hui, Jiang, Yingkui, Dong, Fang, He, Xinhua, Lai, Xiaoshuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
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
Descripción
Sumario: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.