Cargando…

Molecular evidence for an active endogenous microbiome beneath glacial ice

Geologic, chemical and isotopic evidence indicate that Earth has experienced numerous intervals of widespread glaciation throughout its history, with roughly 11% of present day Earth's land surface covered in ice. Despite the pervasive nature of glacial ice both today and in Earth's past a...

Descripción completa

Detalles Bibliográficos
Autores principales: Hamilton, Trinity L, Peters, John W, Skidmore, Mark L, Boyd, Eric S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695297/
https://www.ncbi.nlm.nih.gov/pubmed/23486249
http://dx.doi.org/10.1038/ismej.2013.31
_version_ 1782274953884729344
author Hamilton, Trinity L
Peters, John W
Skidmore, Mark L
Boyd, Eric S
author_facet Hamilton, Trinity L
Peters, John W
Skidmore, Mark L
Boyd, Eric S
author_sort Hamilton, Trinity L
collection PubMed
description Geologic, chemical and isotopic evidence indicate that Earth has experienced numerous intervals of widespread glaciation throughout its history, with roughly 11% of present day Earth's land surface covered in ice. Despite the pervasive nature of glacial ice both today and in Earth's past and the potential contribution of these systems to global biogeochemical cycles, the composition and phylogenetic structure of an active microbial community in subglacial systems has yet to be described. Here, using RNA-based approaches, we demonstrate the presence of active and endogenous archaeal, bacterial and eukaryal assemblages in cold (0–1 °C) subglacial sediments sampled from Robertson Glacier, Alberta, Canada. Patterns in the phylogenetic structure and composition of subglacial sediment small subunit (SSU) ribosomal RNA (rRNA) assemblages indicate greater diversity and evenness than in glacial surface environments, possibly due to facilitative or competitive interactions among populations in the subglacial environment. The combination of phylogenetically more even and more diverse assemblages in the subglacial environment suggests minimal niche overlap and optimization to capture a wider spectrum of the limited nutrients and chemical energy made available from weathering of bedrock minerals. The prevalence of SSU rRNA affiliated with lithoautotrophic bacteria, autotrophic methane producing archaea and heterotrophic eukarya in the subglacial environment is consistent with this hypothesis and suggests an active contribution to the global carbon cycle. Collectively, our findings demonstrate that subglacial environments harbor endogenous active ecosystems that have the potential to impact global biogeochemical cycles over extended periods of time.
format Online
Article
Text
id pubmed-3695297
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-36952972013-07-01 Molecular evidence for an active endogenous microbiome beneath glacial ice Hamilton, Trinity L Peters, John W Skidmore, Mark L Boyd, Eric S ISME J Original Article Geologic, chemical and isotopic evidence indicate that Earth has experienced numerous intervals of widespread glaciation throughout its history, with roughly 11% of present day Earth's land surface covered in ice. Despite the pervasive nature of glacial ice both today and in Earth's past and the potential contribution of these systems to global biogeochemical cycles, the composition and phylogenetic structure of an active microbial community in subglacial systems has yet to be described. Here, using RNA-based approaches, we demonstrate the presence of active and endogenous archaeal, bacterial and eukaryal assemblages in cold (0–1 °C) subglacial sediments sampled from Robertson Glacier, Alberta, Canada. Patterns in the phylogenetic structure and composition of subglacial sediment small subunit (SSU) ribosomal RNA (rRNA) assemblages indicate greater diversity and evenness than in glacial surface environments, possibly due to facilitative or competitive interactions among populations in the subglacial environment. The combination of phylogenetically more even and more diverse assemblages in the subglacial environment suggests minimal niche overlap and optimization to capture a wider spectrum of the limited nutrients and chemical energy made available from weathering of bedrock minerals. The prevalence of SSU rRNA affiliated with lithoautotrophic bacteria, autotrophic methane producing archaea and heterotrophic eukarya in the subglacial environment is consistent with this hypothesis and suggests an active contribution to the global carbon cycle. Collectively, our findings demonstrate that subglacial environments harbor endogenous active ecosystems that have the potential to impact global biogeochemical cycles over extended periods of time. Nature Publishing Group 2013-07 2013-03-14 /pmc/articles/PMC3695297/ /pubmed/23486249 http://dx.doi.org/10.1038/ismej.2013.31 Text en Copyright © 2013 International Society for Microbial Ecology http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Hamilton, Trinity L
Peters, John W
Skidmore, Mark L
Boyd, Eric S
Molecular evidence for an active endogenous microbiome beneath glacial ice
title Molecular evidence for an active endogenous microbiome beneath glacial ice
title_full Molecular evidence for an active endogenous microbiome beneath glacial ice
title_fullStr Molecular evidence for an active endogenous microbiome beneath glacial ice
title_full_unstemmed Molecular evidence for an active endogenous microbiome beneath glacial ice
title_short Molecular evidence for an active endogenous microbiome beneath glacial ice
title_sort molecular evidence for an active endogenous microbiome beneath glacial ice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3695297/
https://www.ncbi.nlm.nih.gov/pubmed/23486249
http://dx.doi.org/10.1038/ismej.2013.31
work_keys_str_mv AT hamiltontrinityl molecularevidenceforanactiveendogenousmicrobiomebeneathglacialice
AT petersjohnw molecularevidenceforanactiveendogenousmicrobiomebeneathglacialice
AT skidmoremarkl molecularevidenceforanactiveendogenousmicrobiomebeneathglacialice
AT boyderics molecularevidenceforanactiveendogenousmicrobiomebeneathglacialice