Literature DB >> 26473717

Contrasting distributions of groundwater arsenic and uranium in the western Hetao basin, Inner Mongolia: Implication for origins and fate controls.

Huaming Guo1, Yongfeng Jia2, Richard B Wanty3, Yuxiao Jiang2, Weiguang Zhao2, Wei Xiu4, Jiaxing Shen2, Yuan Li4, Yongsheng Cao2, Yang Wu5, Di Zhang2, Chao Wei6, Yilong Zhang7, Wengeng Cao7, Andrea Foster8.   

Abstract

Although As concentrations have been investigated in shallow groundwater from the Hetao basin, China, less is known about U and As distributions in deep groundwater, which would help to better understand their origins and fate controls. Two hundred and ninety-nine groundwater samples, 122 sediment samples, and 14 rock samples were taken from the northwest portion of the Hetao basin, and analyzed for geochemical parameters. Results showed contrasting distributions of groundwater U and As, with high U and low As concentrations in the alluvial fans along the basin margins, and low U and high As concentrations downgradient in the flat plain. The probable sources of both As and U in groundwater were ultimately traced to the bedrocks in the local mountains (the Langshan Mountains). Chemical weathering of U-bearing rocks (schist, phyllite, and carbonate veins) released and mobilized U as UO2(CO3)2(2-) and UO2(CO3)3(4-) species in the alluvial fans under oxic conditions and suboxic conditions where reductions of Mn and NO3(-) were favorable (OSO), resulting in high groundwater U concentrations. Conversely, the recent weathering of As-bearing rocks (schist, phyllite, and sulfides) led to the formation of As-bearing Fe(III) (hydr)oxides in sediments, resulting in low groundwater As concentrations. Arsenic mobilization and U immobilization occurred in suboxic conditions where reduction of Fe(III) oxides was favorable and reducing conditions (SOR). Reduction of As-bearing Fe(III) (hydr)oxides, which were formed during palaeo-weathering and transported and deposited as Quaternary aquifer sediments, was believed to release As into groundwater. Reduction of U(VI) to U(IV) would lead to the formation of uraninite, and therefore remove U from groundwater. We conclude that the contrasting distributions of groundwater As and U present a challenge to ensuring safe drinking water in analogous areas, especially with high background values of U and As.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  As species; Coprecipitation; Oxidative dissolution; Redox-sensitive element; Reductive dissolution; U species

Year:  2015        PMID: 26473717     DOI: 10.1016/j.scitotenv.2015.10.018

Source DB:  PubMed          Journal:  Sci Total Environ        ISSN: 0048-9697            Impact factor:   7.963


  3 in total

1.  Overexpression of hsa-miR-186 induces chromosomal instability in arsenic-exposed human keratinocytes.

Authors:  Jiguo Wu; Ana P Ferragut Cardoso; Vanessa A R States; Laila Al-Eryani; Mark Doll; Sandra S Wise; Shesh N Rai; J Christopher States
Journal:  Toxicol Appl Pharmacol       Date:  2019-06-06       Impact factor: 4.219

2.  Risk assessment of fluoride and arsenic in groundwater and a scenario analysis for reducing exposure in Inner Mongolia.

Authors:  Koyomi Nakazawa; Osamu Nagafuchi; Uchralt Otede; Ji-Qun Chen; Koji Kanefuji; Ken'ichi Shinozuka
Journal:  RSC Adv       Date:  2020-05-13       Impact factor: 3.361

3.  Distribution and Geochemical Controls of Arsenic and Uranium in Groundwater-Derived Drinking Water in Bihar, India.

Authors:  Laura A Richards; Arun Kumar; Prabhat Shankar; Aman Gaurav; Ashok Ghosh; David A Polya
Journal:  Int J Environ Res Public Health       Date:  2020-04-06       Impact factor: 3.390

  3 in total

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