Methane in Two Stream Networks: Similar Contributions From Groundwater and Local Sediments While Oxidation Was a Large Sink Controlling Atmospheric Emissions

Abstract Streams are important sources of methane (CH 4 ) to the atmosphere but magnitudes and regulation of stream CH 4 fluxes remain uncertain. Stream CH 4 can come from groundwater and/or produced in anoxic sediments. A fraction can be microbially oxidized to carbon dioxide (CO 2 ) when passing redox gradients in soil, sediment, or water, while the fraction escaping oxidation is emitted to the atmosphere. The relative importance of the CH 4 sources (groundwater inputs vs. sediment production) and the fraction oxidized is typically unknown, yet key for the regulation and magnitude of stream emissions. In this study, we followed the transport of CH 4 from below‐stream soils to the stream water surface and to the atmosphere using a combination of CH 4 concentration and stable carbon isotope gradient measurements, high resolution stream flux and discharge assessments, and inverse mass‐balance modeling. Sampling was done in multiple locations in the stream network of two independent catchments in Sweden to consider spatial variability. We show that the surface water, sub‐surface, and groundwater CH 4 concentration, CH 4 oxidation, and emission were highly variable in space. Our results indicate that the variability could be related to stream morphology and soil characteristics. Of the total CH 4 input into the streams, roughly half of it was estimated to come from groundwater CH 4 in both catchments (39% and 57%; the rest from sediment production), and most of the CH 4 was oxidized (97%–99%) before emission to the atmosphere. Our results indicate that CH 4 oxidation is a major sink for CH 4 in the studied streams.

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Publication Details

Journal
Journal of Geophysical Research Biogeosciences
Published
2024-08-01
DOI
https://doi.org/10.1029/2023jg007836
Citations
4
Primary Topic
Atmospheric and Environmental Gas Dynamics
Type
article
Field-Weighted Citation Impact
1.13

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article

Methane in Two Stream Networks: Similar Contributions From Groundwater and Local Sediments While Oxidation Was a Large Sink Controlling Atmospheric Emissions

Lakshmanan Arunachalam, Leif Klemedtsson, Magnus Gålfalk, V. Geethalakshmi et al.
4 citations
Journal of Geophysical Research Biogeosciences
Atmospheric and Environmental Gas Dynamics
1.13
article

Methane in Two Stream Networks: Similar Contributions From Groundwater and Local Sediments While Oxidation Was a Large Sink Controlling Atmospheric Emissions

Lakshmanan Arunachalam, Leif Klemedtsson, Magnus Gålfalk, V. Geethalakshmi, Balathandayuthabani Panneer Selvam, Sari Peura, David Bastviken, Peter Saetre, Ulrik Kautsky
article en
4 citations

Abstract

Abstract Streams are important sources of methane (CH 4 ) to the atmosphere but magnitudes and regulation of stream CH 4 fluxes remain uncertain. Stream CH 4 can come from groundwater and/or produced in anoxic sediments. A fraction can be microbially oxidized to carbon dioxide (CO 2 ) when passing redox gradients in soil, sediment, or water, while the fraction escaping oxidation is emitted to the atmosphere. The relative importance of the CH 4 sources (groundwater inputs vs. sediment production) and the fraction oxidized is typically unknown, yet key for the regulation and magnitude of stream emissions. In this study, we followed the transport of CH 4 from below‐stream soils to the stream water surface and to the atmosphere using a combination of CH 4 concentration and stable carbon isotope gradient measurements, high resolution stream flux and discharge assessments, and inverse mass‐balance modeling. Sampling was done in multiple locations in the stream network of two independent catchments in Sweden to consider spatial variability. We show that the surface water, sub‐surface, and groundwater CH 4 concentration, CH 4 oxidation, and emission were highly variable in space. Our results indicate that the variability could be related to stream morphology and soil characteristics. Of the total CH 4 input into the streams, roughly half of it was estimated to come from groundwater CH 4 in both catchments (39% and 57%; the rest from sediment production), and most of the CH 4 was oxidized (97%–99%) before emission to the atmosphere. Our results indicate that CH 4 oxidation is a major sink for CH 4 in the studied streams.

Journal of Geophysical Research BiogeosciencesVol. 129(8)
Linköping University (SE), Tamil Nadu Agricultural University (IN), University of Gothenburg (SE), Swedish Nuclear Fuel and Waste Management (Sweden) (SE)
Svenska Forskningsrådet Formas, Svensk Kärnbränslehantering, Vetenskapsrådet, European Research Council
Openalex Percentile: Top 23%
Atmospheric and Environmental Gas Dynamics
1.13
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