Understanding Microbial Arsenic-Mobilization in Multiple Aquifers: Insight from DNA and RNA Analyses
Biogeochemical processes critically control the groundwater arsenic (As) enrichment; however, the key active As-mobilizing biogeochemical processes and associated microbes in high dissolved As and sulfate aquifers are poorly understood. To address this issue, the groundwater-sediment geochemistry, t...
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Veröffentlicht in: | Environmental science & technology 2021-11, Vol.55 (22), p.15181-15195 |
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description | Biogeochemical processes critically control the groundwater arsenic (As) enrichment; however, the key active As-mobilizing biogeochemical processes and associated microbes in high dissolved As and sulfate aquifers are poorly understood. To address this issue, the groundwater-sediment geochemistry, total and active microbial communities, and their potential functions in the groundwater-sediment microbiota from the western Hetao basin were determined using 16S rRNA gene (rDNA) and associated 16S rRNA (rRNA) sequencing. The relative abundances of either sediment or groundwater total and active microbial communities were positively correlated. Interestingly, groundwater active microbial communities were mainly associated with ammonium and sulfide, while sediment active communities were highly related to water-extractable nitrate. Both sediment-sourced and groundwater-sourced active microorganisms (rRNA/rDNA ratios > 1) noted Fe(III)-reducers (induced by ammonium oxidation) and As(V)-reducers, emphasizing the As mobilization via Fe(III) and/or As(V) reduction. Moreover, active cryptic sulfur cycling between groundwater and sediments was implicated in affecting As mobilization. Sediment-sourced active microorganisms were potentially involved in anaerobic pyrite oxidation (driven by denitrification), while groundwater-sourced organisms were associated with sulfur disproportionation and sulfate reduction. This study provides an extended whole-picture concept model of active As–N–S–Fe biogeochemical processes affecting As mobilization in high dissolved As and sulfate aquifers. |
doi_str_mv | 10.1021/acs.est.1c04117 |
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To address this issue, the groundwater-sediment geochemistry, total and active microbial communities, and their potential functions in the groundwater-sediment microbiota from the western Hetao basin were determined using 16S rRNA gene (rDNA) and associated 16S rRNA (rRNA) sequencing. The relative abundances of either sediment or groundwater total and active microbial communities were positively correlated. Interestingly, groundwater active microbial communities were mainly associated with ammonium and sulfide, while sediment active communities were highly related to water-extractable nitrate. Both sediment-sourced and groundwater-sourced active microorganisms (rRNA/rDNA ratios > 1) noted Fe(III)-reducers (induced by ammonium oxidation) and As(V)-reducers, emphasizing the As mobilization via Fe(III) and/or As(V) reduction. Moreover, active cryptic sulfur cycling between groundwater and sediments was implicated in affecting As mobilization. Sediment-sourced active microorganisms were potentially involved in anaerobic pyrite oxidation (driven by denitrification), while groundwater-sourced organisms were associated with sulfur disproportionation and sulfate reduction. This study provides an extended whole-picture concept model of active As–N–S–Fe biogeochemical processes affecting As mobilization in high dissolved As and sulfate aquifers.</description><identifier>ISSN: 0013-936X</identifier><identifier>EISSN: 1520-5851</identifier><identifier>DOI: 10.1021/acs.est.1c04117</identifier><language>eng</language><publisher>Easton: American Chemical Society</publisher><subject>Ammonium ; Anaerobic microorganisms ; Aquifers ; Arsenic ; Biogeochemistry ; Contaminants in Aquatic and Terrestrial Environments ; Denitrification ; Disproportionation ; Geochemistry ; Groundwater ; Iron ; Microbial activity ; Microbiota ; Microorganisms ; Oxidation ; Pyrite ; rRNA 16S ; Sediments ; Sulfate reduction ; Sulfates ; Sulfur</subject><ispartof>Environmental science & technology, 2021-11, Vol.55 (22), p.15181-15195</ispartof><rights>2021 American Chemical Society</rights><rights>Copyright American Chemical Society Nov 16, 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a338t-d78916c2394e1934e563b48564062a234c1e935d618a97de486311292cfd820b3</citedby><cites>FETCH-LOGICAL-a338t-d78916c2394e1934e563b48564062a234c1e935d618a97de486311292cfd820b3</cites><orcidid>0000-0002-4408-8775 ; 0000-0003-4065-5725 ; 0000-0002-4169-0912</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.est.1c04117$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.est.1c04117$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids></links><search><creatorcontrib>Xiu, Wei</creatorcontrib><creatorcontrib>Ke, Tiantian</creatorcontrib><creatorcontrib>Lloyd, Jonathan R</creatorcontrib><creatorcontrib>Shen, Jiaxing</creatorcontrib><creatorcontrib>Bassil, Naji M</creatorcontrib><creatorcontrib>Song, Hokyung</creatorcontrib><creatorcontrib>Polya, David A</creatorcontrib><creatorcontrib>Zhao, Yi</creatorcontrib><creatorcontrib>Guo, Huaming</creatorcontrib><title>Understanding Microbial Arsenic-Mobilization in Multiple Aquifers: Insight from DNA and RNA Analyses</title><title>Environmental science & technology</title><addtitle>Environ. Sci. Technol</addtitle><description>Biogeochemical processes critically control the groundwater arsenic (As) enrichment; however, the key active As-mobilizing biogeochemical processes and associated microbes in high dissolved As and sulfate aquifers are poorly understood. To address this issue, the groundwater-sediment geochemistry, total and active microbial communities, and their potential functions in the groundwater-sediment microbiota from the western Hetao basin were determined using 16S rRNA gene (rDNA) and associated 16S rRNA (rRNA) sequencing. The relative abundances of either sediment or groundwater total and active microbial communities were positively correlated. Interestingly, groundwater active microbial communities were mainly associated with ammonium and sulfide, while sediment active communities were highly related to water-extractable nitrate. Both sediment-sourced and groundwater-sourced active microorganisms (rRNA/rDNA ratios > 1) noted Fe(III)-reducers (induced by ammonium oxidation) and As(V)-reducers, emphasizing the As mobilization via Fe(III) and/or As(V) reduction. Moreover, active cryptic sulfur cycling between groundwater and sediments was implicated in affecting As mobilization. Sediment-sourced active microorganisms were potentially involved in anaerobic pyrite oxidation (driven by denitrification), while groundwater-sourced organisms were associated with sulfur disproportionation and sulfate reduction. This study provides an extended whole-picture concept model of active As–N–S–Fe biogeochemical processes affecting As mobilization in high dissolved As and sulfate aquifers.</description><subject>Ammonium</subject><subject>Anaerobic microorganisms</subject><subject>Aquifers</subject><subject>Arsenic</subject><subject>Biogeochemistry</subject><subject>Contaminants in Aquatic and Terrestrial Environments</subject><subject>Denitrification</subject><subject>Disproportionation</subject><subject>Geochemistry</subject><subject>Groundwater</subject><subject>Iron</subject><subject>Microbial activity</subject><subject>Microbiota</subject><subject>Microorganisms</subject><subject>Oxidation</subject><subject>Pyrite</subject><subject>rRNA 16S</subject><subject>Sediments</subject><subject>Sulfate reduction</subject><subject>Sulfates</subject><subject>Sulfur</subject><issn>0013-936X</issn><issn>1520-5851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kM9LwzAUx4MoOKdnrwEvgnTmJU2aeCvz12BTEAVvJWtTzejSLWkP8683ZeJB8PR4vM_3y-OD0DmQCRAK17oMExO6CZQkBcgO0Ag4JQmXHA7RiBBgiWLi_RidhLAihFBG5AhVb64yPnTaVdZ94IUtfbu0usG5D8bZMlnEtbFfurOtw9bhRd90dtMYnG97W8foDZ65YD8-O1z7do1vn3Icy_BLnLnTzS6YcIqOat0Ec_Yzx-jt_u51-pjMnx9m03yeaMZkl1SZVCBKylRqQLHUcMGWqeQiJYJqytISjGK8EiC1yiqTSsEAqKJlXUlKlmyMLve9G99u-yijWNtQmqbRzrR9KCiXWSY4pyKiF3_QVdv7-O9AKSUYB64idb2nopUQvKmLjbdr7XcFkGKwXkTrxZD-sR4TV_vEcPit_I_-BnXEgzc</recordid><startdate>20211116</startdate><enddate>20211116</enddate><creator>Xiu, Wei</creator><creator>Ke, Tiantian</creator><creator>Lloyd, Jonathan R</creator><creator>Shen, Jiaxing</creator><creator>Bassil, Naji M</creator><creator>Song, Hokyung</creator><creator>Polya, David A</creator><creator>Zhao, Yi</creator><creator>Guo, Huaming</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4408-8775</orcidid><orcidid>https://orcid.org/0000-0003-4065-5725</orcidid><orcidid>https://orcid.org/0000-0002-4169-0912</orcidid></search><sort><creationdate>20211116</creationdate><title>Understanding Microbial Arsenic-Mobilization in Multiple Aquifers: Insight from DNA and RNA Analyses</title><author>Xiu, Wei ; Ke, Tiantian ; Lloyd, Jonathan R ; Shen, Jiaxing ; Bassil, Naji M ; Song, Hokyung ; Polya, David A ; Zhao, Yi ; Guo, Huaming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a338t-d78916c2394e1934e563b48564062a234c1e935d618a97de486311292cfd820b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Ammonium</topic><topic>Anaerobic microorganisms</topic><topic>Aquifers</topic><topic>Arsenic</topic><topic>Biogeochemistry</topic><topic>Contaminants in Aquatic and Terrestrial Environments</topic><topic>Denitrification</topic><topic>Disproportionation</topic><topic>Geochemistry</topic><topic>Groundwater</topic><topic>Iron</topic><topic>Microbial activity</topic><topic>Microbiota</topic><topic>Microorganisms</topic><topic>Oxidation</topic><topic>Pyrite</topic><topic>rRNA 16S</topic><topic>Sediments</topic><topic>Sulfate reduction</topic><topic>Sulfates</topic><topic>Sulfur</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiu, Wei</creatorcontrib><creatorcontrib>Ke, Tiantian</creatorcontrib><creatorcontrib>Lloyd, Jonathan R</creatorcontrib><creatorcontrib>Shen, Jiaxing</creatorcontrib><creatorcontrib>Bassil, Naji M</creatorcontrib><creatorcontrib>Song, Hokyung</creatorcontrib><creatorcontrib>Polya, David A</creatorcontrib><creatorcontrib>Zhao, Yi</creatorcontrib><creatorcontrib>Guo, Huaming</creatorcontrib><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental science & technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiu, Wei</au><au>Ke, Tiantian</au><au>Lloyd, Jonathan R</au><au>Shen, Jiaxing</au><au>Bassil, Naji M</au><au>Song, Hokyung</au><au>Polya, David A</au><au>Zhao, Yi</au><au>Guo, Huaming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Understanding Microbial Arsenic-Mobilization in Multiple Aquifers: Insight from DNA and RNA Analyses</atitle><jtitle>Environmental science & technology</jtitle><addtitle>Environ. Sci. Technol</addtitle><date>2021-11-16</date><risdate>2021</risdate><volume>55</volume><issue>22</issue><spage>15181</spage><epage>15195</epage><pages>15181-15195</pages><issn>0013-936X</issn><eissn>1520-5851</eissn><abstract>Biogeochemical processes critically control the groundwater arsenic (As) enrichment; however, the key active As-mobilizing biogeochemical processes and associated microbes in high dissolved As and sulfate aquifers are poorly understood. To address this issue, the groundwater-sediment geochemistry, total and active microbial communities, and their potential functions in the groundwater-sediment microbiota from the western Hetao basin were determined using 16S rRNA gene (rDNA) and associated 16S rRNA (rRNA) sequencing. The relative abundances of either sediment or groundwater total and active microbial communities were positively correlated. Interestingly, groundwater active microbial communities were mainly associated with ammonium and sulfide, while sediment active communities were highly related to water-extractable nitrate. Both sediment-sourced and groundwater-sourced active microorganisms (rRNA/rDNA ratios > 1) noted Fe(III)-reducers (induced by ammonium oxidation) and As(V)-reducers, emphasizing the As mobilization via Fe(III) and/or As(V) reduction. Moreover, active cryptic sulfur cycling between groundwater and sediments was implicated in affecting As mobilization. Sediment-sourced active microorganisms were potentially involved in anaerobic pyrite oxidation (driven by denitrification), while groundwater-sourced organisms were associated with sulfur disproportionation and sulfate reduction. 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subjects | Ammonium Anaerobic microorganisms Aquifers Arsenic Biogeochemistry Contaminants in Aquatic and Terrestrial Environments Denitrification Disproportionation Geochemistry Groundwater Iron Microbial activity Microbiota Microorganisms Oxidation Pyrite rRNA 16S Sediments Sulfate reduction Sulfates Sulfur |
title | Understanding Microbial Arsenic-Mobilization in Multiple Aquifers: Insight from DNA and RNA Analyses |
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