The provenance of deep groundwater and its relation to arsenic distribution in the northwestern Hetao Basin, Inner Mongolia

被引:8
|
作者
Liu, Shuai [1 ,2 ]
Guo, Huaming [1 ,2 ]
Lu, Hai [3 ]
Zhang, Zhuo [2 ]
Zhao, Weiguang [2 ]
机构
[1] China Univ Geosci, State Key Lab Biogeol & Environm Geol, Beijing 100083, Peoples R China
[2] China Univ Geosci Beijing, Sch Water Resources & Environm, Beijing 100083, Peoples R China
[3] Natl Inst Metrol, Beijing 100013, Peoples R China
基金
中国国家自然科学基金;
关键词
Deep groundwater; High As; Sources; Sr-87; Sr-86; Hydrogeological processes; STRONTIUM ISOTOPES; SHALLOW AQUIFERS; SR-87/SR-86; RATIOS; ORGANIC-MATTER; TRACE-ELEMENTS; CHINA EVIDENCE; WATER SOURCES; FLOW PATHS; MOBILIZATION; SR;
D O I
10.1007/s10653-019-00433-0
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
High-arsenic (As) groundwater has been widely found throughout the world. The source of groundwater would determine spatial distribution of groundwater As. In order to trace the source of high-As deep groundwater (DGW, depths > 50 m), groundwater, sediments, and local bedrock samples were taken to investigate chemical and isotopic compositions in the Hetao Basin, China. Results showed that Sr-87/Sr-86 in DGW gradually decreased with the increase in As concentrations along the approximate flow path. In recharge-oxic zone (Zone I), DGW was mainly recharged by fissure water, influenced mostly by weathering of phyllite bedrock and meta-basalt. In groundwater flow-moderate reducing zone (Zone II), DGW was mainly related to incongruent dissolution of feldspar. However, in groundwater flow-reducing zone (Zone III), DGW was partly recharged from shallow groundwater (SGW) with depths < 50 m. The mixing contributions of SGW to DGW in Zone III mostly exceeded 80% during groundwater irrigation season. In Zone I, DGW As concentrations were mostly lower than 50 mu g/L due to oxic conditions. In Zone II, the weakly alkaline pH and the decreasing Ca/Na resulting from incongruent dissolution of feldspar caused As desorption, which was the major contribution to As mobilization (As mostly > 200 mu g/L). In Zone III, the recharge of SGW introduced labile organic matter to support reduction of Fe(III) oxyhydroxides/oxides and predominantly led to As release into groundwater (As > 300 mu g/L). This study has provided insights into the source of high-As DGW and the effect of SGW mixing on As mobilization.
引用
收藏
页码:1429 / 1451
页数:23
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