Cargando…

Geological activity shapes the microbiome in deep-subsurface aquifers by advection

Subsurface environments host diverse microorganisms in fluid-filled fractures; however, little is known about how geological and hydrological processes shape the subterranean biosphere. Here, we sampled three flowing boreholes weekly for 10 mo in a 1478-m-deep fractured rock aquifer to study the rol...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Yuran, Horne, Roland N., Hawkins, Adam J., Primo, John Carlo, Gorbatenko, Oxana, Dekas, Anne E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231496/
https://www.ncbi.nlm.nih.gov/pubmed/35696589
http://dx.doi.org/10.1073/pnas.2113985119
_version_ 1784735355687141376
author Zhang, Yuran
Horne, Roland N.
Hawkins, Adam J.
Primo, John Carlo
Gorbatenko, Oxana
Dekas, Anne E.
author_facet Zhang, Yuran
Horne, Roland N.
Hawkins, Adam J.
Primo, John Carlo
Gorbatenko, Oxana
Dekas, Anne E.
author_sort Zhang, Yuran
collection PubMed
description Subsurface environments host diverse microorganisms in fluid-filled fractures; however, little is known about how geological and hydrological processes shape the subterranean biosphere. Here, we sampled three flowing boreholes weekly for 10 mo in a 1478-m-deep fractured rock aquifer to study the role of fracture activity (defined as seismically or aseismically induced fracture aperture change) and advection on fluid-associated microbial community composition. We found that despite a largely stable deep-subsurface fluid microbiome, drastic community-level shifts occurred after events signifying physical changes in the permeable fracture network. The community-level shifts include the emergence of microbial families from undetected to over 50% relative abundance, as well as the replacement of the community in one borehole by the earlier community from a different borehole. Null-model analysis indicates that the observed spatial and temporal community turnover was primarily driven by stochastic processes (as opposed to deterministic processes). We, therefore, conclude that the observed community-level shifts resulted from the physical transport of distinct microbial communities from other fracture(s) that outpaced environmental selection. Given that geological activity is a major cause of fracture activity and that geological activity is ubiquitous across space and time on Earth, our findings suggest that advection induced by geological activity is a general mechanism shaping the microbial biogeography and diversity in deep-subsurface habitats across the globe.
format Online
Article
Text
id pubmed-9231496
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher National Academy of Sciences
record_format MEDLINE/PubMed
spelling pubmed-92314962022-06-25 Geological activity shapes the microbiome in deep-subsurface aquifers by advection Zhang, Yuran Horne, Roland N. Hawkins, Adam J. Primo, John Carlo Gorbatenko, Oxana Dekas, Anne E. Proc Natl Acad Sci U S A Biological Sciences Subsurface environments host diverse microorganisms in fluid-filled fractures; however, little is known about how geological and hydrological processes shape the subterranean biosphere. Here, we sampled three flowing boreholes weekly for 10 mo in a 1478-m-deep fractured rock aquifer to study the role of fracture activity (defined as seismically or aseismically induced fracture aperture change) and advection on fluid-associated microbial community composition. We found that despite a largely stable deep-subsurface fluid microbiome, drastic community-level shifts occurred after events signifying physical changes in the permeable fracture network. The community-level shifts include the emergence of microbial families from undetected to over 50% relative abundance, as well as the replacement of the community in one borehole by the earlier community from a different borehole. Null-model analysis indicates that the observed spatial and temporal community turnover was primarily driven by stochastic processes (as opposed to deterministic processes). We, therefore, conclude that the observed community-level shifts resulted from the physical transport of distinct microbial communities from other fracture(s) that outpaced environmental selection. Given that geological activity is a major cause of fracture activity and that geological activity is ubiquitous across space and time on Earth, our findings suggest that advection induced by geological activity is a general mechanism shaping the microbial biogeography and diversity in deep-subsurface habitats across the globe. National Academy of Sciences 2022-06-13 2022-06-21 /pmc/articles/PMC9231496/ /pubmed/35696589 http://dx.doi.org/10.1073/pnas.2113985119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Zhang, Yuran
Horne, Roland N.
Hawkins, Adam J.
Primo, John Carlo
Gorbatenko, Oxana
Dekas, Anne E.
Geological activity shapes the microbiome in deep-subsurface aquifers by advection
title Geological activity shapes the microbiome in deep-subsurface aquifers by advection
title_full Geological activity shapes the microbiome in deep-subsurface aquifers by advection
title_fullStr Geological activity shapes the microbiome in deep-subsurface aquifers by advection
title_full_unstemmed Geological activity shapes the microbiome in deep-subsurface aquifers by advection
title_short Geological activity shapes the microbiome in deep-subsurface aquifers by advection
title_sort geological activity shapes the microbiome in deep-subsurface aquifers by advection
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9231496/
https://www.ncbi.nlm.nih.gov/pubmed/35696589
http://dx.doi.org/10.1073/pnas.2113985119
work_keys_str_mv AT zhangyuran geologicalactivityshapesthemicrobiomeindeepsubsurfaceaquifersbyadvection
AT hornerolandn geologicalactivityshapesthemicrobiomeindeepsubsurfaceaquifersbyadvection
AT hawkinsadamj geologicalactivityshapesthemicrobiomeindeepsubsurfaceaquifersbyadvection
AT primojohncarlo geologicalactivityshapesthemicrobiomeindeepsubsurfaceaquifersbyadvection
AT gorbatenkooxana geologicalactivityshapesthemicrobiomeindeepsubsurfaceaquifersbyadvection
AT dekasannee geologicalactivityshapesthemicrobiomeindeepsubsurfaceaquifersbyadvection