Geochemical Evolution of Groundwater Flowing Through Arsenic Source Sediments in an Aquifer System of West Bengal, India

The source of geogenic arsenic (As) contaminating a shallow aquifer in West Bengal was traced to fine‐grained sediments deposited in an abandoned river channel. Along with As‐bearing phases, these sediments contain 0.46% codeposited organic carbon. The release of As and the geochemistry of groundwat...

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Veröffentlicht in:Water resources research 2017-11, Vol.53 (11), p.8715-8735
Hauptverfasser: Desbarats, A. J., Pal, T., Mukherjee, P. K., Beckie, R. D.
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container_issue 11
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creator Desbarats, A. J.
Pal, T.
Mukherjee, P. K.
Beckie, R. D.
description The source of geogenic arsenic (As) contaminating a shallow aquifer in West Bengal was traced to fine‐grained sediments deposited in an abandoned river channel. Along with As‐bearing phases, these sediments contain 0.46% codeposited organic carbon. The release of As and the geochemistry of groundwater within the channel‐fill deposits is investigated using a detailed mass balance model supported by aqueous, solid‐phase, and mineralogical data. The model describes the evolution of groundwater chemistry along a flow path extending from its recharge in an abandoned channel pond, through the channel fill, to the underlying aquifer. Variations in groundwater composition are explained in terms of mineral weathering of host sediments driven by organic carbon decay. Arsenic is released through the reductive dissolution of goethite and the weathering of chlorite. Concomitantly, some As is sequestered in precipitating vivianite. These competing processes reach equilibrium deeper in the channel‐fill sequence as groundwater As concentrations stabilize. The model yields estimates of mineral reaction (or precipitation) rates including rates of organic carbon oxidation (1.15 mmol C L−1 a−1) and net As release ( 4.57×10−4 mmol L−1 a−1). Fine‐grained, slightly permeable, deposits such as channel fill containing reactive organic carbon and As‐bearing goethite and phyllosilicates are centers of intense chemical weathering conducive to As mobilization. Plain Language Summary Groundwater contamination by geogenic arsenic is impacting the health of over 100 million people across Asia. According to the World Health Organization, this is the largest mass poisoning in history. To advance understanding of the arsenic source and fundamental processes involved in its release, scientists from the Geological Surveys of Canada and India, and the University of British Columbia, undertook a joint research project in an affected village of West Bengal. This paper describes the geochemical evolution of groundwater as it flows through arsenic source sediments deposited in an abandoned river meander. A mass balance model was developed to explain groundwater composition and arsenic release in terms of the dissolution or precipitation of minerals found in the sediments. This study has yielded new knowledge of arsenic hosts and release processes, and it represents an important step toward the development of sound public health mitigation schemes in India and elsewhere. Key Points Chemical weather
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J. ; Pal, T. ; Mukherjee, P. K. ; Beckie, R. D.</creator><creatorcontrib>Desbarats, A. J. ; Pal, T. ; Mukherjee, P. K. ; Beckie, R. D.</creatorcontrib><description>The source of geogenic arsenic (As) contaminating a shallow aquifer in West Bengal was traced to fine‐grained sediments deposited in an abandoned river channel. Along with As‐bearing phases, these sediments contain 0.46% codeposited organic carbon. The release of As and the geochemistry of groundwater within the channel‐fill deposits is investigated using a detailed mass balance model supported by aqueous, solid‐phase, and mineralogical data. The model describes the evolution of groundwater chemistry along a flow path extending from its recharge in an abandoned channel pond, through the channel fill, to the underlying aquifer. Variations in groundwater composition are explained in terms of mineral weathering of host sediments driven by organic carbon decay. Arsenic is released through the reductive dissolution of goethite and the weathering of chlorite. Concomitantly, some As is sequestered in precipitating vivianite. These competing processes reach equilibrium deeper in the channel‐fill sequence as groundwater As concentrations stabilize. The model yields estimates of mineral reaction (or precipitation) rates including rates of organic carbon oxidation (1.15 mmol C L−1 a−1) and net As release ( 4.57×10−4 mmol L−1 a−1). Fine‐grained, slightly permeable, deposits such as channel fill containing reactive organic carbon and As‐bearing goethite and phyllosilicates are centers of intense chemical weathering conducive to As mobilization. Plain Language Summary Groundwater contamination by geogenic arsenic is impacting the health of over 100 million people across Asia. According to the World Health Organization, this is the largest mass poisoning in history. To advance understanding of the arsenic source and fundamental processes involved in its release, scientists from the Geological Surveys of Canada and India, and the University of British Columbia, undertook a joint research project in an affected village of West Bengal. This paper describes the geochemical evolution of groundwater as it flows through arsenic source sediments deposited in an abandoned river meander. A mass balance model was developed to explain groundwater composition and arsenic release in terms of the dissolution or precipitation of minerals found in the sediments. This study has yielded new knowledge of arsenic hosts and release processes, and it represents an important step toward the development of sound public health mitigation schemes in India and elsewhere. Key Points Chemical weathering of goethite and chlorite in channel‐fill silts releases As Some released As is resequestered in precipitating vivianite The net arsenic release rate from source sediments is 34 μg L−1 a−1</description><identifier>ISSN: 0043-1397</identifier><identifier>EISSN: 1944-7973</identifier><identifier>DOI: 10.1002/2017WR020863</identifier><language>eng</language><publisher>Washington: John Wiley &amp; Sons, Inc</publisher><subject>Aquifer systems ; Aquifers ; Arsenic ; Carbon ; Chemical precipitation ; Chemical weathering ; Chlorite ; Codeposition ; Contamination ; Dissolution ; Dissolving ; Educational institutions ; Evolution ; Fluvial deposits ; Fluvial sediments ; Geochemistry ; Geological surveys ; Goethite ; Groundwater ; Groundwater chemistry ; Groundwater composition ; Groundwater pollution ; Hosts ; India ; Mass ; Mass balance models ; Minerals ; Mitigation ; Organic carbon ; Organizations ; Oxidation ; Precipitation ; Public health ; Research projects ; River channels ; River meanders ; Rivers ; Sediment ; Sediments ; Studies ; Surveys ; Vivianite ; Weathering</subject><ispartof>Water resources research, 2017-11, Vol.53 (11), p.8715-8735</ispartof><rights>2017. American Geophysical Union and Her Majesty the Queen in Right of Canada. Reproduced with the permission of the Geological Survey of Canada, the Geological Survey of India, and the University of British Columbia.</rights><rights>2017. American Geophysical Union. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a3309-f6649eaa9fd69ac94b4e6c31739e8ad7d2e06dce983fb5b9925b83797361a1f73</citedby><cites>FETCH-LOGICAL-a3309-f6649eaa9fd69ac94b4e6c31739e8ad7d2e06dce983fb5b9925b83797361a1f73</cites><orcidid>0000-0003-3909-4166 ; 0000-0001-6152-4420</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F2017WR020863$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F2017WR020863$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,11494,27903,27904,45553,45554,46447,46871</link.rule.ids></links><search><creatorcontrib>Desbarats, A. J.</creatorcontrib><creatorcontrib>Pal, T.</creatorcontrib><creatorcontrib>Mukherjee, P. K.</creatorcontrib><creatorcontrib>Beckie, R. D.</creatorcontrib><title>Geochemical Evolution of Groundwater Flowing Through Arsenic Source Sediments in an Aquifer System of West Bengal, India</title><title>Water resources research</title><description>The source of geogenic arsenic (As) contaminating a shallow aquifer in West Bengal was traced to fine‐grained sediments deposited in an abandoned river channel. Along with As‐bearing phases, these sediments contain 0.46% codeposited organic carbon. The release of As and the geochemistry of groundwater within the channel‐fill deposits is investigated using a detailed mass balance model supported by aqueous, solid‐phase, and mineralogical data. The model describes the evolution of groundwater chemistry along a flow path extending from its recharge in an abandoned channel pond, through the channel fill, to the underlying aquifer. Variations in groundwater composition are explained in terms of mineral weathering of host sediments driven by organic carbon decay. Arsenic is released through the reductive dissolution of goethite and the weathering of chlorite. Concomitantly, some As is sequestered in precipitating vivianite. These competing processes reach equilibrium deeper in the channel‐fill sequence as groundwater As concentrations stabilize. The model yields estimates of mineral reaction (or precipitation) rates including rates of organic carbon oxidation (1.15 mmol C L−1 a−1) and net As release ( 4.57×10−4 mmol L−1 a−1). Fine‐grained, slightly permeable, deposits such as channel fill containing reactive organic carbon and As‐bearing goethite and phyllosilicates are centers of intense chemical weathering conducive to As mobilization. Plain Language Summary Groundwater contamination by geogenic arsenic is impacting the health of over 100 million people across Asia. According to the World Health Organization, this is the largest mass poisoning in history. To advance understanding of the arsenic source and fundamental processes involved in its release, scientists from the Geological Surveys of Canada and India, and the University of British Columbia, undertook a joint research project in an affected village of West Bengal. This paper describes the geochemical evolution of groundwater as it flows through arsenic source sediments deposited in an abandoned river meander. A mass balance model was developed to explain groundwater composition and arsenic release in terms of the dissolution or precipitation of minerals found in the sediments. This study has yielded new knowledge of arsenic hosts and release processes, and it represents an important step toward the development of sound public health mitigation schemes in India and elsewhere. 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J.</au><au>Pal, T.</au><au>Mukherjee, P. K.</au><au>Beckie, R. D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Geochemical Evolution of Groundwater Flowing Through Arsenic Source Sediments in an Aquifer System of West Bengal, India</atitle><jtitle>Water resources research</jtitle><date>2017-11</date><risdate>2017</risdate><volume>53</volume><issue>11</issue><spage>8715</spage><epage>8735</epage><pages>8715-8735</pages><issn>0043-1397</issn><eissn>1944-7973</eissn><abstract>The source of geogenic arsenic (As) contaminating a shallow aquifer in West Bengal was traced to fine‐grained sediments deposited in an abandoned river channel. Along with As‐bearing phases, these sediments contain 0.46% codeposited organic carbon. The release of As and the geochemistry of groundwater within the channel‐fill deposits is investigated using a detailed mass balance model supported by aqueous, solid‐phase, and mineralogical data. The model describes the evolution of groundwater chemistry along a flow path extending from its recharge in an abandoned channel pond, through the channel fill, to the underlying aquifer. Variations in groundwater composition are explained in terms of mineral weathering of host sediments driven by organic carbon decay. Arsenic is released through the reductive dissolution of goethite and the weathering of chlorite. Concomitantly, some As is sequestered in precipitating vivianite. These competing processes reach equilibrium deeper in the channel‐fill sequence as groundwater As concentrations stabilize. The model yields estimates of mineral reaction (or precipitation) rates including rates of organic carbon oxidation (1.15 mmol C L−1 a−1) and net As release ( 4.57×10−4 mmol L−1 a−1). Fine‐grained, slightly permeable, deposits such as channel fill containing reactive organic carbon and As‐bearing goethite and phyllosilicates are centers of intense chemical weathering conducive to As mobilization. Plain Language Summary Groundwater contamination by geogenic arsenic is impacting the health of over 100 million people across Asia. According to the World Health Organization, this is the largest mass poisoning in history. To advance understanding of the arsenic source and fundamental processes involved in its release, scientists from the Geological Surveys of Canada and India, and the University of British Columbia, undertook a joint research project in an affected village of West Bengal. This paper describes the geochemical evolution of groundwater as it flows through arsenic source sediments deposited in an abandoned river meander. A mass balance model was developed to explain groundwater composition and arsenic release in terms of the dissolution or precipitation of minerals found in the sediments. This study has yielded new knowledge of arsenic hosts and release processes, and it represents an important step toward the development of sound public health mitigation schemes in India and elsewhere. Key Points Chemical weathering of goethite and chlorite in channel‐fill silts releases As Some released As is resequestered in precipitating vivianite The net arsenic release rate from source sediments is 34 μg L−1 a−1</abstract><cop>Washington</cop><pub>John Wiley &amp; Sons, Inc</pub><doi>10.1002/2017WR020863</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0003-3909-4166</orcidid><orcidid>https://orcid.org/0000-0001-6152-4420</orcidid></addata></record>
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subjects Aquifer systems
Aquifers
Arsenic
Carbon
Chemical precipitation
Chemical weathering
Chlorite
Codeposition
Contamination
Dissolution
Dissolving
Educational institutions
Evolution
Fluvial deposits
Fluvial sediments
Geochemistry
Geological surveys
Goethite
Groundwater
Groundwater chemistry
Groundwater composition
Groundwater pollution
Hosts
India
Mass
Mass balance models
Minerals
Mitigation
Organic carbon
Organizations
Oxidation
Precipitation
Public health
Research projects
River channels
River meanders
Rivers
Sediment
Sediments
Studies
Surveys
Vivianite
Weathering
title Geochemical Evolution of Groundwater Flowing Through Arsenic Source Sediments in an Aquifer System of West Bengal, India
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