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Glodowska, Martyna; Stopelli, Emiliano; Schneider, Magnus; Rathi, Bhasker; Straub, Daniel; Lightfoot, Alex; Kipfer, Rolf; Berg, Michael; Jetten, Mike S M; Kleindienst, Sara; Kappler, Andreas (2020): Arsenic mobilization by anaerobic iron-dependent methane oxidation [dataset bundled publication]. PANGAEA, https://doi.org/10.1594/PANGAEA.924771

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Abstract:
Arsenic groundwater contamination is threatening the health of millions of people worldwide, particularly in river deltas in South and Southeast Asia where geogenic arsenic is released from sediments1-5. In most cases, the release of arsenic (As) was shown to be caused by microbially catalyzed reductive dissolution of As-bearing Fe(III) (oxyhydr)oxide minerals with organic carbon being used as microbial electron and energy source6-8. Although in many As-contaminated aquifers high concentrations of methane (CH4) were observed9-11, the role of CH4 for As mobilization is unknown. Here we demonstrate that CH4 functions as electron donor for methanotrophic microorganisms and triggers the reductive dissolution of As-bearing Fe(III) (oxyhydr)oxide minerals leading to As mobilization. In microcosms with As-bearing sediments from the Red River Delta amended with environmentally relevant concentrations of CH4 we found that CH4 triggers Fe(III) mineral reduction, supports the growth and activity of type-1 aerobic methanotrophs and archaea affiliating with Candidatus Methanoperedens, increases the abundance of methane oxidation mcrA and pmoA genes, and ultimately mobilizes significant amount of As into the water. Our findings provide evidence for a methane-mediated mechanism for arsenic mobilization that is distinct from previously described pathways. Taking this together with the common presence of methane in arsenic-contaminated aquifers, we suggest that this methane-driven arsenic mobilization may contribute to arsenic contamination of groundwater on a global scale.
Keyword(s):
aquifers; arsenic; contamination; groundwater; iron; Methane; microorganisms
Supplement to:
Glodowska, Martyna; Stopelli, Emiliano; Schneider, Magnus; Rathi, Bhasker; Straub, Daniel; Lightfoot, Alex; Kipfer, Rolf; Berg, Michael; Jetten, Mike S M; Kleindienst, Sara; Kappler, Andreas; AdvectAs Team Members (2020): Arsenic mobilization by anaerobic iron-dependent methane oxidation. Communications Earth & Environment, 1, 42, https://doi.org/10.1038/s43247-020-00037-y
Coverage:
Latitude: 20.922167 * Longitude: 105.894000
Date/Time Start: 2018-11-06T10:34:42 * Date/Time End: 2018-11-26T11:38:52
Size:
10 datasets

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Datasets listed in this bundled publication

  1. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Ferrozine spectroscopy data corresponding to concentrations of Fe(II)/Fe(total) ratio. https://doi.org/10.1594/PANGAEA.924873
  2. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Ferrozine spectroscopy data corresponding to concentrations of Fe(II) in sediment. https://doi.org/10.1594/PANGAEA.924803
  3. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Ferrozine spectroscopy data corresponding to concentrations of Fe(II) in solution. https://doi.org/10.1594/PANGAEA.924906
  4. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Ferrozine spectroscopy data corresponding to concentrations of Fe(total) in sediment. https://doi.org/10.1594/PANGAEA.924807
  5. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Field gas measurements from wells in Van Phuc village, Hanoi, Vietnam. https://doi.org/10.1594/PANGAEA.924680
  6. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Hydrochemical data of samples from Van Phuc village, Hanoi, Vietnam. https://doi.org/10.1594/PANGAEA.924685
  7. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Quantitative PCR data corresponding to archaea 16S genes. https://doi.org/10.1594/PANGAEA.924773
  8. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Quantitative PCR data corresponding to bacteria 16S genes. https://doi.org/10.1594/PANGAEA.924777
  9. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Quantitative PCR data corresponding to methyl-coenzyme M reductase subunit alpha (mcrA) genes. https://doi.org/10.1594/PANGAEA.924778
  10. Glodowska, M; Stopelli, E; Schneider, M et al. (2020): Quantitative PCR data corresponding to particulate methane monooxygenase (pmoA) genes. https://doi.org/10.1594/PANGAEA.924779