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Visualizing Methane-Cycling Microbial Dynamics in Coastal Wetlands
Published on: January 31, 2025
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Microbial contributions to subterranean methane sinks
J T Lennon1, D Nguyễn-Thùy2, T M Phạm3
1Department of Biology, Indiana University, Bloomington, IN, USA.
Geobiology
|September 28, 2016
Summary
Cave ecosystems may act as methane sinks due to microbial oxidation, not radiolysis. Methanotrophic bacteria consume methane in caves at significant rates, impacting global methane cycles.
Area of Science:
- Biogeochemistry
- Microbial Ecology
- Environmental Science
Background:
- Methane (CH4) sources and sinks are crucial for global biogeochemical cycles and climate change.
- Cave ecosystems often show depleted CH4 concentrations, suggesting they may be CH4 sinks.
- Two hypotheses explain this depletion: abiotic radiolysis and biotic oxidation by methanotrophic bacteria.
Purpose of the Study:
- To investigate the cause of methane depletion in cave ecosystems.
- To evaluate the radiolysis hypothesis for methane loss.
- To assess the role of microbial methanotrophy in subterranean methane cycling.
Main Methods:
- Theoretical kinetic analysis of the radiolysis hypothesis.
- Laboratory experiments to validate radiolysis constraints.
- Mesocosm experiments in Vietnamese caves to quantify microbial methane oxidation.
Main Results:
- Radiolysis is a kinetically constrained process unlikely to cause rapid methane loss in caves.
- Methanotrophic bacteria in cave rocks consume methane at rates of 1.3-2.7 mg CH4 · m-2 · d-1.
- Observed methane oxidation rates in caves are comparable to or exceed those in other terrestrial ecosystems.
Conclusions:
- Microbial oxidation by methanotrophic bacteria is the primary driver of methane depletion in caves.
- Subterranean microbial methanotrophy can significantly impact atmospheric methane concentrations.
- Further research is needed to understand the broader implications of subterranean methane oxidation on global methane budgets.
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