3 results on '"Chen, Yongchun"'
Search Results
2. Quantitative identification of nitrate and sulfate sources of a multiple land-use area impacted by mine drainage.
- Author
-
Chen, Xing, Zheng, Liugen, Zhu, Manzhou, Jiang, Chunlu, Dong, Xianglin, and Chen, Yongchun
- Subjects
- *
MINE drainage , *SULFATES , *FERTILIZERS , *NITRATES , *SULFUR cycle , *MANURES , *COAL mining - Abstract
The rapid increase in urbanization and intensive coal mining activities have accelerated the deterioration of surface water quality. Environmental problems caused by the accumulation of nitrate and sulfate from natural, urban, and agricultural sources have attracted extensive attention. Information on nitrate and sulfate sources and their transformations is crucial for understanding the nitrogen and sulfur cycles in surface water. In this study, we monitored nitrate and sulfate in three representative rivers in mining cities in northern China. The main pollution sources and biogeochemical processes were identified by using stable isotopes (δD, δ18O H2O , δ15N, δ18O NO3 , δ34S and δ18O SO4) and hydrochemistry. The contribution of natural and anthropogenic sources was quantitatively estimated based on a Bayesian mixed model. The results indicated a large variation in sulfate and nitrate sources between the different rivers. Nitrate in the Tuohe River mainly derived from manure/sewage (57.9%) and soil N (26.9%), while sulfate mainly derived from manure/sewage (41.7%) and evaporite dissolution (26.8%). For the Suihe River, nitrate was primarily sourced from chemical fertilizer (37.9%) and soil nitrogen (34.8%), while sulfate was mainly sourced from manure/sewage (33.1%) and chemical fertilizer (21.4%). For the Huihe River, nitrate mainly derived from mine drainage (56.6%) and manure/sewage (30.6%), while sulfate predominantly originated from mine drainage (58.3%) and evaporite dissolution (12.9%). Microbial nitrification was the major pathway for the migration and transformation of nitrate in the surface water. However, denitrification and bacterial sulfate reduction (BSR) did not play a significant role as aerobic conditions prevailed. In this study, we elucidated the sources and transformation mechanisms of nitrate and sulfate. Additionally, we provided a reference for formulating a comprehensive strategy for effective management and remediation of surface water contaminated with nitrate and sulfate in mining cities. [Display omitted] • Natural and anthropogenic sources of nitrates and sulfates were quantified. • Water from the Tuohe, Suihe, and Huihe Rivers and a subsidence zone were studied. • Nitrification was the major pathway for nitrate transformation in surface water. • Multiple sources of pollutants could be identified simultaneously. • Denitrification and bacterial sulfate reduction (BSR) were not observed. [ABSTRACT FROM AUTHOR]
- Published
- 2023
- Full Text
- View/download PDF
3. Nitrate sources and transformations in surface water of a mining area due to intensive mining activities: Emphasis on effects on distinct subsidence waters.
- Author
-
Hu, Jie, Chen, Xing, Chen, Yeyu, Li, Chang, Ren, Mengxi, Jiang, Chunlu, Chen, Yongchun, An, Shikai, Xu, Yanfei, and Zheng, Liugen
- Subjects
- *
STRIP mining , *MINE water , *MINE drainage , *LAND subsidence , *MINES & mineral resources , *MANURES - Abstract
The increase in NO 3 − content in surface water caused by intensive mining activities in Huainan City, China, has attracted considerable attention owing to the deterioration of water quality and the degradation of ecosystems in recent years. The Huainan mining area, which is highly disturbed by anthropogenic activities, was selected as a typical observation area, and the surface water was classified as open subsidence water (OSW), closed subsidence water (CSW), and river water (RW). Moreover, the hydrochemical parameters and the δ15N and δ18O values of nitrate were employed to quantitatively trace the sources and biochemical transformation of NO 3 −, and the contribution ratios of different NO 3 − sources were estimated using the stable isotope analysis in R based on the Bayesian model. There was evident nitrification in the study area, but no significant denitrification has occurred. A substantial portion of δ15N–NO 3 - demonstrated complex sources of NO 3 −. Compared with those of CSW, the NO 3 − compositions of the OSW approached to those of the RW due to river recharge and discharge, and were greatly affected by anthropogenic activities. The proportional contribution of manure and sewage in the OSW was found to be the highest with a mean value of 39.5 % ± 12.3 %, which was followed by that of mine drainage (mean: 22.1 % ± 13.1 %), chemical fertilizer (mean: 17.5 % ± 10.6 %), and soil organic nitrogen (mean: 17.5 % ± 11.6 %). In the RW, the highest mean contribution of manure sewage was 35.2 % ± 9.7 %, which was followed by that of chemical fertilizer (mean: 29.3 % ± 7.2 %), mine drainage (mean: 23.4 % ± 13.0 %), and soil organic nitrogen (mean: 10.9 % ± 8.3 %). In contrast, the contribution of chemical fertilizer to the CSW was the highest with a mean value of 33.9 % ± 13.6 %, which was followed by that of soil organic nitrogen (mean: 26.5 % ± 13.8 %), mine drainage (mean: 18.1 % ± 11.6 %). Therefore, NO 3 − in the surface water of the mining area primarily originates from chemical fertilizers and manure sewage. In addition, the contribution of mine drainage to nitrate in the study area indicates the potential impact of mining activities on surface water. These findings highlight the value of classifying different types of surface water in tracing NO 3 − contamination sources, and provide relevant theoretical basis for tracing nitrate sources in other areas. [Display omitted] • The sources of NO 3 − were identified by hydrochemistry and dual isotopes. • There were similar NO 3 − sources in rivers and open subsidence area. • Chemical fertilizer, manure and sewage were the main NO 3 − sources in mining area. [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
- View/download PDF
Catalog
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.