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Biogeochemical Cycling by a Low-Diversity Microbial Community in Deep Groundwater
Olkiluoto, an island on the south-west coast of Finland, will host a deep geological repository for the storage of spent nuclear fuel. Microbially induced corrosion from the generation of sulphide is therefore a concern as it could potentially compromise the longevity of the copper waste canisters....
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137086/ https://www.ncbi.nlm.nih.gov/pubmed/30245678 http://dx.doi.org/10.3389/fmicb.2018.02129 |
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author | Bell, Emma Lamminmäki, Tiina Alneberg, Johannes Andersson, Anders F. Qian, Chen Xiong, Weili Hettich, Robert L. Balmer, Louise Frutschi, Manon Sommer, Guillaume Bernier-Latmani, Rizlan |
author_facet | Bell, Emma Lamminmäki, Tiina Alneberg, Johannes Andersson, Anders F. Qian, Chen Xiong, Weili Hettich, Robert L. Balmer, Louise Frutschi, Manon Sommer, Guillaume Bernier-Latmani, Rizlan |
author_sort | Bell, Emma |
collection | PubMed |
description | Olkiluoto, an island on the south-west coast of Finland, will host a deep geological repository for the storage of spent nuclear fuel. Microbially induced corrosion from the generation of sulphide is therefore a concern as it could potentially compromise the longevity of the copper waste canisters. Groundwater at Olkiluoto is geochemically stratified with depth and elevated concentrations of sulphide are observed when sulphate-rich and methane-rich groundwaters mix. Particularly high sulphide is observed in methane-rich groundwater from a fracture at 530.6 mbsl, where mixing with sulphate-rich groundwater occurred as the result of an open drill hole connecting two different fractures at different depths. To determine the electron donors fuelling sulphidogenesis, we combined geochemical, isotopic, metagenomic and metaproteomic analyses. This revealed a low diversity microbial community fuelled by hydrogen and organic carbon. Sulphur and carbon isotopes of sulphate and dissolved inorganic carbon, respectively, confirmed that sulphate reduction was ongoing and that CO(2) came from the degradation of organic matter. The results demonstrate the impact of introducing sulphate to a methane-rich groundwater with limited electron acceptors and provide insight into extant metabolisms in the terrestrial subsurface. |
format | Online Article Text |
id | pubmed-6137086 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61370862018-09-21 Biogeochemical Cycling by a Low-Diversity Microbial Community in Deep Groundwater Bell, Emma Lamminmäki, Tiina Alneberg, Johannes Andersson, Anders F. Qian, Chen Xiong, Weili Hettich, Robert L. Balmer, Louise Frutschi, Manon Sommer, Guillaume Bernier-Latmani, Rizlan Front Microbiol Microbiology Olkiluoto, an island on the south-west coast of Finland, will host a deep geological repository for the storage of spent nuclear fuel. Microbially induced corrosion from the generation of sulphide is therefore a concern as it could potentially compromise the longevity of the copper waste canisters. Groundwater at Olkiluoto is geochemically stratified with depth and elevated concentrations of sulphide are observed when sulphate-rich and methane-rich groundwaters mix. Particularly high sulphide is observed in methane-rich groundwater from a fracture at 530.6 mbsl, where mixing with sulphate-rich groundwater occurred as the result of an open drill hole connecting two different fractures at different depths. To determine the electron donors fuelling sulphidogenesis, we combined geochemical, isotopic, metagenomic and metaproteomic analyses. This revealed a low diversity microbial community fuelled by hydrogen and organic carbon. Sulphur and carbon isotopes of sulphate and dissolved inorganic carbon, respectively, confirmed that sulphate reduction was ongoing and that CO(2) came from the degradation of organic matter. The results demonstrate the impact of introducing sulphate to a methane-rich groundwater with limited electron acceptors and provide insight into extant metabolisms in the terrestrial subsurface. Frontiers Media S.A. 2018-09-07 /pmc/articles/PMC6137086/ /pubmed/30245678 http://dx.doi.org/10.3389/fmicb.2018.02129 Text en Copyright © 2018 Bell, Lamminmäki, Alneberg, Andersson, Qian, Xiong, Hettich, Balmer, Frutschi, Sommer and Bernier-Latmani. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Bell, Emma Lamminmäki, Tiina Alneberg, Johannes Andersson, Anders F. Qian, Chen Xiong, Weili Hettich, Robert L. Balmer, Louise Frutschi, Manon Sommer, Guillaume Bernier-Latmani, Rizlan Biogeochemical Cycling by a Low-Diversity Microbial Community in Deep Groundwater |
title | Biogeochemical Cycling by a Low-Diversity Microbial Community in Deep Groundwater |
title_full | Biogeochemical Cycling by a Low-Diversity Microbial Community in Deep Groundwater |
title_fullStr | Biogeochemical Cycling by a Low-Diversity Microbial Community in Deep Groundwater |
title_full_unstemmed | Biogeochemical Cycling by a Low-Diversity Microbial Community in Deep Groundwater |
title_short | Biogeochemical Cycling by a Low-Diversity Microbial Community in Deep Groundwater |
title_sort | biogeochemical cycling by a low-diversity microbial community in deep groundwater |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6137086/ https://www.ncbi.nlm.nih.gov/pubmed/30245678 http://dx.doi.org/10.3389/fmicb.2018.02129 |
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