Tracing microbial carbon sources in hydrothermal sediments by C isotopic analysis of bacterial and archaeal ribosomal RNA.

Fuente: PubMed
Salvato in:
Dettagli Bibliografici
Autori principali: MacGregor, Barbara, Boschker, Henricus T S, Hoer, Daniel, Albert, Daniel B, Mendlovitz, Howard, Teske, Andreas
Natura: Artículo científico
Lingua:en
Pubblicazione: Frontiers in microbiology 2025
Accesso online:
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne!!
_version_ 1868266132930035713
author MacGregor, Barbara
Boschker, Henricus T S
Hoer, Daniel
Albert, Daniel B
Mendlovitz, Howard
Teske, Andreas
author_facet MacGregor, Barbara
Boschker, Henricus T S
Hoer, Daniel
Albert, Daniel B
Mendlovitz, Howard
Teske, Andreas
MacGregor, Barbara
Boschker, Henricus T S
Hoer, Daniel
Albert, Daniel B
Mendlovitz, Howard
Teske, Andreas
collection PubMed - marine biology
contents Tracing microbial carbon sources in hydrothermal sediments by C isotopic analysis of bacterial and archaeal ribosomal RNA. MacGregor, Barbara Boschker, Henricus T S Hoer, Daniel Albert, Daniel B Mendlovitz, Howard Teske, Andreas Microbial communities in hydrothermal sediments of Guaymas Basin assimilate a wide range of carbon sources, detrital organic matter, DIC of hydrothermal and water column origin, as well as methane, light alkanes and petroleum hydrocarbons. Here we analyze the abundances and C-isotopic values of these carbon pools, and assess the relative importance of these carbon sources by comparison with δC-isotopic composition of bacterial and archaeal rRNA. In almost all hydrothermal sediments, δC-rRNA values for bacterial and archaea are lighter (more C-depleted) than those of TOC and DIC, indicating that carbon from C-depleted methane permeates the microbial food web, with no systematic preference for bacteria or archaea. However, the omnipresence of detrital organic matter of photosynthetic origin means that any methane signal in bacterial and archaeal δC-rRNA values is diluted by the heterotrophic background. In non-hydrothermal background sediment where methane is lacking, the δC-rRNA values for bacterial and archaea are heavier (less C-depleted) and indicate the preferential utilization of detrital TOC of photosynthetic origin. The presence of petroleum in some methane-rich hydrothermal cores does not visibly change the δC-rRNA values for bacterial and archaea, since the δC-isotopic composition of hydrothermal petroleum in Guaymas Basin is similar to its source, detrital organic carbon, and thus does not separate fossil carbon utilizers from general heterotrophs. When δC-depleted methane competes with high concentrations of δC-repleted (heavier) short-chain alkanes, δC-rRNA values for bacteria and archaea are noticeably heavier than those in methane-rich but alkane-poor sediments, suggesting short-chain alkane incorporation. Under alkane-rich conditions, consistent differences between bacterial and archaea δC-rRNA were observed, suggesting the impact of distinct bacterial and archaeal alkane assimilation pathways. To summarize, we note that the availability of different sedimentary or hydrothermal carbon sources-in particular hydrothermal methane-is reflected in changing δC-rRNA values for bacteria and archaea.
format Artículo científico
id pubmed_41178965
institution PubMed
language en
publishDate 2025
publisher Frontiers in microbiology
record_format pubmed
spellingShingle Tracing microbial carbon sources in hydrothermal sediments by C isotopic analysis of bacterial and archaeal ribosomal RNA.
MacGregor, Barbara
Boschker, Henricus T S
Hoer, Daniel
Albert, Daniel B
Mendlovitz, Howard
Teske, Andreas
Tracing microbial carbon sources in hydrothermal sediments by C isotopic analysis of bacterial and archaeal ribosomal RNA. MacGregor, Barbara Boschker, Henricus T S Hoer, Daniel Albert, Daniel B Mendlovitz, Howard Teske, Andreas Microbial communities in hydrothermal sediments of Guaymas Basin assimilate a wide range of carbon sources, detrital organic matter, DIC of hydrothermal and water column origin, as well as methane, light alkanes and petroleum hydrocarbons. Here we analyze the abundances and C-isotopic values of these carbon pools, and assess the relative importance of these carbon sources by comparison with δC-isotopic composition of bacterial and archaeal rRNA. In almost all hydrothermal sediments, δC-rRNA values for bacterial and archaea are lighter (more C-depleted) than those of TOC and DIC, indicating that carbon from C-depleted methane permeates the microbial food web, with no systematic preference for bacteria or archaea. However, the omnipresence of detrital organic matter of photosynthetic origin means that any methane signal in bacterial and archaeal δC-rRNA values is diluted by the heterotrophic background. In non-hydrothermal background sediment where methane is lacking, the δC-rRNA values for bacterial and archaea are heavier (less C-depleted) and indicate the preferential utilization of detrital TOC of photosynthetic origin. The presence of petroleum in some methane-rich hydrothermal cores does not visibly change the δC-rRNA values for bacterial and archaea, since the δC-isotopic composition of hydrothermal petroleum in Guaymas Basin is similar to its source, detrital organic carbon, and thus does not separate fossil carbon utilizers from general heterotrophs. When δC-depleted methane competes with high concentrations of δC-repleted (heavier) short-chain alkanes, δC-rRNA values for bacteria and archaea are noticeably heavier than those in methane-rich but alkane-poor sediments, suggesting short-chain alkane incorporation. Under alkane-rich conditions, consistent differences between bacterial and archaea δC-rRNA were observed, suggesting the impact of distinct bacterial and archaeal alkane assimilation pathways. To summarize, we note that the availability of different sedimentary or hydrothermal carbon sources-in particular hydrothermal methane-is reflected in changing δC-rRNA values for bacteria and archaea.
title Tracing microbial carbon sources in hydrothermal sediments by C isotopic analysis of bacterial and archaeal ribosomal RNA.
url https://pubmed.ncbi.nlm.nih.gov/41178965/