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Auteurs principaux: Leung, Pok Man, Jeffrey, Luke C, Bay, Sean K, Gomez-Alvarez, Paula, Hall, Montgomery, Johnston, Scott G, Dittmann, Johannes, Deschaseaux, Elisabeth, Hopkins, Billie, Haskell, Jasmine, Jirapanjawat, Thanavit, Hutchinson, Tess F, Coleman, Nicholas V, Dong, Xiyang, Maher, Damien T, Greening, Chris
Format: Artículo científico
Langue:en
Publié: Science (New York, N.Y.) 2026
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Accès en ligne:https://pubmed.ncbi.nlm.nih.gov/41505541/
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author Leung, Pok Man
Jeffrey, Luke C
Bay, Sean K
Gomez-Alvarez, Paula
Hall, Montgomery
Johnston, Scott G
Dittmann, Johannes
Deschaseaux, Elisabeth
Hopkins, Billie
Haskell, Jasmine
Jirapanjawat, Thanavit
Hutchinson, Tess F
Coleman, Nicholas V
Dong, Xiyang
Maher, Damien T
Greening, Chris
author_facet Leung, Pok Man
Jeffrey, Luke C
Bay, Sean K
Gomez-Alvarez, Paula
Hall, Montgomery
Johnston, Scott G
Dittmann, Johannes
Deschaseaux, Elisabeth
Hopkins, Billie
Haskell, Jasmine
Jirapanjawat, Thanavit
Hutchinson, Tess F
Coleman, Nicholas V
Dong, Xiyang
Maher, Damien T
Greening, Chris
Leung, Pok Man
Jeffrey, Luke C
Bay, Sean K
Gomez-Alvarez, Paula
Hall, Montgomery
Johnston, Scott G
Dittmann, Johannes
Deschaseaux, Elisabeth
Hopkins, Billie
Haskell, Jasmine
Jirapanjawat, Thanavit
Hutchinson, Tess F
Coleman, Nicholas V
Dong, Xiyang
Maher, Damien T
Greening, Chris
collection PubMed - marine biology
contents Bark microbiota modulate climate-active gas fluxes in Australian forests. Leung, Pok Man Jeffrey, Luke C Bay, Sean K Gomez-Alvarez, Paula Hall, Montgomery Johnston, Scott G Dittmann, Johannes Deschaseaux, Elisabeth Hopkins, Billie Haskell, Jasmine Jirapanjawat, Thanavit Hutchinson, Tess F Coleman, Nicholas V Dong, Xiyang Maher, Damien T Greening, Chris Methane Plant Bark Australia Microbiota Forests Hydrogen Carbon Monoxide Metagenomics Trees Bacteria Anaerobiosis Recent studies suggest that microbes inhabit tree bark, yet little is known about their identities, functions, and environmental roles. Here we reveal, through gene-centric and genome-resolved metagenomics, that the bark of eight common Australian tree species hosts abundant and specialized microbial communities. The predominant bacteria are hydrogen-cycling facultative anaerobes adapted to dynamic redox and substrate conditions. Furthermore, bark-associated methanotrophs are abundant and can coexist with hydrogenotrophic methanogens. Microcosm experiments showed that bark microorganisms aerobically consume methane, hydrogen, and carbon monoxide at in planta concentrations and produce these gases under anoxia. Combined with in situ field measurements, we show that tree-dwelling microbiota metabolize multiple climate-active gases at marked rates within tree stems, highlighting a potentially substantial role in global atmospheric cycles.
format Artículo científico
id pubmed_41505541
institution PubMed
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publishDate 2026
publisher Science (New York, N.Y.)
record_format pubmed
spellingShingle Bark microbiota modulate climate-active gas fluxes in Australian forests.
Leung, Pok Man
Jeffrey, Luke C
Bay, Sean K
Gomez-Alvarez, Paula
Hall, Montgomery
Johnston, Scott G
Dittmann, Johannes
Deschaseaux, Elisabeth
Hopkins, Billie
Haskell, Jasmine
Jirapanjawat, Thanavit
Hutchinson, Tess F
Coleman, Nicholas V
Dong, Xiyang
Maher, Damien T
Greening, Chris
Methane
Plant Bark
Australia
Microbiota
Forests
Hydrogen
Carbon Monoxide
Metagenomics
Trees
Bacteria
Anaerobiosis
Bark microbiota modulate climate-active gas fluxes in Australian forests. Leung, Pok Man Jeffrey, Luke C Bay, Sean K Gomez-Alvarez, Paula Hall, Montgomery Johnston, Scott G Dittmann, Johannes Deschaseaux, Elisabeth Hopkins, Billie Haskell, Jasmine Jirapanjawat, Thanavit Hutchinson, Tess F Coleman, Nicholas V Dong, Xiyang Maher, Damien T Greening, Chris Methane Plant Bark Australia Microbiota Forests Hydrogen Carbon Monoxide Metagenomics Trees Bacteria Anaerobiosis Recent studies suggest that microbes inhabit tree bark, yet little is known about their identities, functions, and environmental roles. Here we reveal, through gene-centric and genome-resolved metagenomics, that the bark of eight common Australian tree species hosts abundant and specialized microbial communities. The predominant bacteria are hydrogen-cycling facultative anaerobes adapted to dynamic redox and substrate conditions. Furthermore, bark-associated methanotrophs are abundant and can coexist with hydrogenotrophic methanogens. Microcosm experiments showed that bark microorganisms aerobically consume methane, hydrogen, and carbon monoxide at in planta concentrations and produce these gases under anoxia. Combined with in situ field measurements, we show that tree-dwelling microbiota metabolize multiple climate-active gases at marked rates within tree stems, highlighting a potentially substantial role in global atmospheric cycles.
title Bark microbiota modulate climate-active gas fluxes in Australian forests.
topic Methane
Plant Bark
Australia
Microbiota
Forests
Hydrogen
Carbon Monoxide
Metagenomics
Trees
Bacteria
Anaerobiosis
url https://pubmed.ncbi.nlm.nih.gov/41505541/