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

Author:

Balathandayuthabani S.12ORCID,Panneer Selvam B.2,Gålfalk M.2,Saetre P.3,Peura S.3,Kautsky U.3,Klemedtsson L.4ORCID,Arunachalam L.1,Vellingiri G.1,Bastviken D.2ORCID

Affiliation:

1. Tamil Nadu Agricultural University Coimbatore India

2. Department of Thematic Studies – Environmental Change Linköping University Linköping Sweden

3. Swedish Nuclear Fuel and Waste Management Company Solna Sweden

4. Department of Earth Sciences University of Gothenburg Gothenburg Sweden

Abstract

AbstractStreams are important sources of methane (CH4) to the atmosphere but magnitudes and regulation of stream CH4 fluxes remain uncertain. Stream CH4 can come from groundwater and/or produced in anoxic sediments. A fraction can be microbially oxidized to carbon dioxide (CO2) when passing redox gradients in soil, sediment, or water, while the fraction escaping oxidation is emitted to the atmosphere. The relative importance of the CH4 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 CH4 from below‐stream soils to the stream water surface and to the atmosphere using a combination of CH4 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 CH4 concentration, CH4 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 CH4 input into the streams, roughly half of it was estimated to come from groundwater CH4 in both catchments (39% and 57%; the rest from sediment production), and most of the CH4 was oxidized (97%–99%) before emission to the atmosphere. Our results indicate that CH4 oxidation is a major sink for CH4 in the studied streams.

Funder

Svensk Kärnbränslehantering

Svenska Forskningsrådet Formas

Vetenskapsrådet

European Research Council

Publisher

American Geophysical Union (AGU)

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