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ORIGINAL RESEARCH article

Front. Microbiol.

Sec. Terrestrial Microbiology

Volume 16 - 2025 | doi: 10.3389/fmicb.2025.1657143

This article is part of the Research TopicUnveiling Microbiome Interactions and Functions in Soil HotspotsView all 13 articles

Microbial and Chemical Predictors of Methane Release from a Stratified Thermokarst Permafrost Hotspot Authors

Provisionally accepted
Kevin  S RozmiarekKevin S Rozmiarek1,2Jihoon  YangJihoon Yang3Jenna  SchambachJenna Schambach4Haley  BennettHaley Bennett4Tristan  A CaroTristan A Caro1Jason  SammonJason Sammon4Joshua  J WhitingJoshua J Whiting4Philip  R MillerPhilip R Miller4J.  Bryce RickenJ. Bryce Ricken4Lisa  BiglerLisa Bigler4Richard  S JayneRichard S Jayne4David  FukuyamaDavid Fukuyama4Tyler  JonesTyler Jones2Chuck  Randall SmallwoodChuck Randall Smallwood5*
  • 1University of Colorado Boulder, Boulder, United States
  • 2University of Colorado Boulder Institute of Arctic and Alpine Research, Boulder, United States
  • 3Sandia National Laboratories California, Livermore, United States
  • 4Sandia National Laboratories, Albuquerque, United States
  • 5Sandia National Laboratories (DOE), Albuquerque, United States

The final, formatted version of the article will be published soon.

Soils are dynamic interfaces that can act as both sources and sinks of methane (CH₄), yet the microbial processes underlying these fluxes remain poorly constrained in current Earth system models—particularly in thawing permafrost regions. Accurately quantifying subsurface microbial activity and its response to environmental variation is essential for improving predictions of CH₄ emissions under shifting temperature regimes. Here, we explore the potential of volatile organic compounds (VOCs) as early chemical indicators of microbial processes driving CH₄ production within a thermokarst-associated CH₄ hotspot. Field surveys at Big Trail Lake, a young thermokarst feature in central Alaska, identified localized CH₄ emission zones. Anaerobic soil laboratory microcosms from 50, 200, and 400 cm depths were incubated at -4°C, 5°C, and 12°C to simulate freeze–thaw transitions. Methane flux increased markedly with temperature, and microbial community shifts revealed Methanosarcina spp. as the dominant methanogen, particularly at 200 cm. VOC profiling showed strong depth- and temperature-dependent patterns, with the 50 cm layer exhibiting the greatest chemical diversity. Notably, 200 cm soils produced VOC signatures overlapping with those from pure Methanosarcina acetivorans C2A cultures, supporting the identification of shared metabolites linked to active methanogenesis. Extended 60-day incubations confirmed temperature-sensitive CH₄ production. Carbon isotopic enrichment in CH₄ was unexpectedly strong with warming, and metagenomic detection of ANME-associated markers–including multiheme cytochromes and formate dehydrogenases–supports temperature-sensitive anaerobic oxidation of methane as a significant control on isotopic signatures. Calculated Q₁₀ values for methanogenesis exceeded typical values for boreal soils, highlighting an underappreciated temperature responsiveness of Arctic methanogens. Together, these results demonstrate that VOCs can serve as informative biomarkers of subsurface microbial activation and offer a novel diagnostic tool for detecting early-stage CH₄ hotspot formation. Incorporating such chemically and biologically resolved metrics into process-based models will be critical for improving forecasts of CH₄ release from thawing permafrost landscapes.

Keywords: methane hotspot, Thermokarst soils, methanotrophy, Microbial VOCs, Permafrost thaw, Biogeochemical modeling, Methane isotopes, carbon cycling

Received: 01 Jul 2025; Accepted: 26 Aug 2025.

Copyright: © 2025 Rozmiarek, Yang, Schambach, Bennett, Caro, Sammon, Whiting, Miller, Ricken, Bigler, Jayne, Fukuyama, Jones and Smallwood. 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) or licensor 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.

* Correspondence: Chuck Randall Smallwood, Sandia National Laboratories (DOE), Albuquerque, United States

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