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Microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of New Caledonia
The southeastern part of New Caledonia main island (Grande Terre) is the location of a large ophiolitic formation that hosts several hyperalkaline springs discharging high pH (∼11) and warm (<40°C) fluids enriched in methane (CH(4)) and hydrogen (H(2)). These waters are produced by the serpentini...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359428/ https://www.ncbi.nlm.nih.gov/pubmed/37485525 http://dx.doi.org/10.3389/fmicb.2023.1196516 |
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author | Quéméneur, Marianne Mei, Nan Monnin, Christophe Postec, Anne Guasco, Sophie Jeanpert, Julie Maurizot, Pierre Pelletier, Bernard Erauso, Gaël |
author_facet | Quéméneur, Marianne Mei, Nan Monnin, Christophe Postec, Anne Guasco, Sophie Jeanpert, Julie Maurizot, Pierre Pelletier, Bernard Erauso, Gaël |
author_sort | Quéméneur, Marianne |
collection | PubMed |
description | The southeastern part of New Caledonia main island (Grande Terre) is the location of a large ophiolitic formation that hosts several hyperalkaline springs discharging high pH (∼11) and warm (<40°C) fluids enriched in methane (CH(4)) and hydrogen (H(2)). These waters are produced by the serpentinization of the ultrabasic rock formations. Molecular surveys had previously revealed the prokaryotic diversity of some of these New Caledonian springs, especially from the submarine chimneys of Prony Bay hydrothermal field. Here we investigate the microbial community of hyperalkaline waters from on-land springs and their relationships with elevated concentrations of dissolved H(2) (21.1–721.3 μmol/L) and CH(4) (153.0–376.6 μmol/L). 16S rRNA gene analyses (metabarcoding and qPCR) provided evidence of abundant and diverse prokaryotic communities inhabiting hyperalkaline fluids at all the collected springs. The abundance of prokaryotes was positively correlated to the H(2)/CH(4) ratio. Prokaryotes consisted mainly of bacteria that use H(2) as an energy source, such as microaerophilic Hydrogenophaga/Serpentinimonas (detected in all sources on land) or anaerobic sulfate-reducing Desulfonatronum, which were exclusively found in the most reducing (E(h) ref H(2) ∼ -700 mV) and the most H(2)-enriched waters discharging at the intertidal spring of the Bain des Japonais. The relative abundance of a specific group of uncultured Methanosarcinales that thrive in serpentinization-driven ecosystems emitting H(2), considered potential H(2)-consuming methanogens, was positively correlated with CH(4) concentrations, and negatively correlated to the relative abundance of methylotrophic Gammaproteobacteria. Firmicutes were also numerous in hyperalkaline waters, and their relative abundance (e.g., Gracilibacter or Dethiobacter) was proportional to the dissolved H(2) concentrations, but their role in the H(2) budget remains to be assessed. The prokaryotic communities thriving in New Caledonia hyperalkaline waters are similar to those found in other serpentinite-hosted high-pH waters worldwide, such as Lost City (North Atlantic) and The Cedars (California). |
format | Online Article Text |
id | pubmed-10359428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103594282023-07-22 Microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of New Caledonia Quéméneur, Marianne Mei, Nan Monnin, Christophe Postec, Anne Guasco, Sophie Jeanpert, Julie Maurizot, Pierre Pelletier, Bernard Erauso, Gaël Front Microbiol Microbiology The southeastern part of New Caledonia main island (Grande Terre) is the location of a large ophiolitic formation that hosts several hyperalkaline springs discharging high pH (∼11) and warm (<40°C) fluids enriched in methane (CH(4)) and hydrogen (H(2)). These waters are produced by the serpentinization of the ultrabasic rock formations. Molecular surveys had previously revealed the prokaryotic diversity of some of these New Caledonian springs, especially from the submarine chimneys of Prony Bay hydrothermal field. Here we investigate the microbial community of hyperalkaline waters from on-land springs and their relationships with elevated concentrations of dissolved H(2) (21.1–721.3 μmol/L) and CH(4) (153.0–376.6 μmol/L). 16S rRNA gene analyses (metabarcoding and qPCR) provided evidence of abundant and diverse prokaryotic communities inhabiting hyperalkaline fluids at all the collected springs. The abundance of prokaryotes was positively correlated to the H(2)/CH(4) ratio. Prokaryotes consisted mainly of bacteria that use H(2) as an energy source, such as microaerophilic Hydrogenophaga/Serpentinimonas (detected in all sources on land) or anaerobic sulfate-reducing Desulfonatronum, which were exclusively found in the most reducing (E(h) ref H(2) ∼ -700 mV) and the most H(2)-enriched waters discharging at the intertidal spring of the Bain des Japonais. The relative abundance of a specific group of uncultured Methanosarcinales that thrive in serpentinization-driven ecosystems emitting H(2), considered potential H(2)-consuming methanogens, was positively correlated with CH(4) concentrations, and negatively correlated to the relative abundance of methylotrophic Gammaproteobacteria. Firmicutes were also numerous in hyperalkaline waters, and their relative abundance (e.g., Gracilibacter or Dethiobacter) was proportional to the dissolved H(2) concentrations, but their role in the H(2) budget remains to be assessed. The prokaryotic communities thriving in New Caledonia hyperalkaline waters are similar to those found in other serpentinite-hosted high-pH waters worldwide, such as Lost City (North Atlantic) and The Cedars (California). Frontiers Media S.A. 2023-07-06 /pmc/articles/PMC10359428/ /pubmed/37485525 http://dx.doi.org/10.3389/fmicb.2023.1196516 Text en Copyright © 2023 Quéméneur, Mei, Monnin, Postec, Guasco, Jeanpert, Maurizot, Pelletier and Erauso. https://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 Quéméneur, Marianne Mei, Nan Monnin, Christophe Postec, Anne Guasco, Sophie Jeanpert, Julie Maurizot, Pierre Pelletier, Bernard Erauso, Gaël Microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of New Caledonia |
title | Microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of New Caledonia |
title_full | Microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of New Caledonia |
title_fullStr | Microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of New Caledonia |
title_full_unstemmed | Microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of New Caledonia |
title_short | Microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of New Caledonia |
title_sort | microbial taxa related to natural hydrogen and methane emissions in serpentinite-hosted hyperalkaline springs of new caledonia |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10359428/ https://www.ncbi.nlm.nih.gov/pubmed/37485525 http://dx.doi.org/10.3389/fmicb.2023.1196516 |
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