S. Balathandayuthabani, B. Panneer Selvam, M. Gålfalk, P. Saetre, S. Peura, U. Kautsky, L. Klemedtsson, L. Arunachalam, G. Vellingiri, D. Bastviken
{"title":"两个溪流网络中的甲烷:地下水和当地沉积物对甲烷的贡献相似,而氧化作用是控制大气排放的一大吸收池","authors":"S. Balathandayuthabani, B. Panneer Selvam, M. Gålfalk, P. Saetre, S. Peura, U. Kautsky, L. Klemedtsson, L. Arunachalam, G. Vellingiri, D. Bastviken","doi":"10.1029/2023JG007836","DOIUrl":null,"url":null,"abstract":"<p>Streams are important sources of methane (CH<sub>4</sub>) to the atmosphere but magnitudes and regulation of stream CH<sub>4</sub> fluxes remain uncertain. Stream CH<sub>4</sub> can come from groundwater and/or produced in anoxic sediments. A fraction can be microbially oxidized to carbon dioxide (CO<sub>2</sub>) 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<sub>4</sub> 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<sub>4</sub> from below-stream soils to the stream water surface and to the atmosphere using a combination of CH<sub>4</sub> 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<sub>4</sub> concentration, CH<sub>4</sub> 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<sub>4</sub> input into the streams, roughly half of it was estimated to come from groundwater CH<sub>4</sub> in both catchments (39% and 57%; the rest from sediment production), and most of the CH<sub>4</sub> was oxidized (97%–99%) before emission to the atmosphere. Our results indicate that CH<sub>4</sub> oxidation is a major sink for CH<sub>4</sub> in the studied streams.</p>","PeriodicalId":16003,"journal":{"name":"Journal of Geophysical Research: Biogeosciences","volume":"129 8","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1029/2023JG007836","citationCount":"0","resultStr":"{\"title\":\"Methane in Two Stream Networks: Similar Contributions From Groundwater and Local Sediments While Oxidation Was a Large Sink Controlling Atmospheric Emissions\",\"authors\":\"S. Balathandayuthabani, B. Panneer Selvam, M. Gålfalk, P. Saetre, S. Peura, U. Kautsky, L. Klemedtsson, L. Arunachalam, G. Vellingiri, D. Bastviken\",\"doi\":\"10.1029/2023JG007836\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Streams are important sources of methane (CH<sub>4</sub>) to the atmosphere but magnitudes and regulation of stream CH<sub>4</sub> fluxes remain uncertain. Stream CH<sub>4</sub> can come from groundwater and/or produced in anoxic sediments. A fraction can be microbially oxidized to carbon dioxide (CO<sub>2</sub>) 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<sub>4</sub> 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<sub>4</sub> from below-stream soils to the stream water surface and to the atmosphere using a combination of CH<sub>4</sub> 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<sub>4</sub> concentration, CH<sub>4</sub> 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<sub>4</sub> input into the streams, roughly half of it was estimated to come from groundwater CH<sub>4</sub> in both catchments (39% and 57%; the rest from sediment production), and most of the CH<sub>4</sub> was oxidized (97%–99%) before emission to the atmosphere. 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Methane in Two Stream Networks: Similar Contributions From Groundwater and Local Sediments While Oxidation Was a Large Sink Controlling Atmospheric Emissions
Streams 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.
期刊介绍:
JGR-Biogeosciences focuses on biogeosciences of the Earth system in the past, present, and future and the extension of this research to planetary studies. The emerging field of biogeosciences spans the intellectual interface between biology and the geosciences and attempts to understand the functions of the Earth system across multiple spatial and temporal scales. Studies in biogeosciences may use multiple lines of evidence drawn from diverse fields to gain a holistic understanding of terrestrial, freshwater, and marine ecosystems and extreme environments. Specific topics within the scope of the section include process-based theoretical, experimental, and field studies of biogeochemistry, biogeophysics, atmosphere-, land-, and ocean-ecosystem interactions, biomineralization, life in extreme environments, astrobiology, microbial processes, geomicrobiology, and evolutionary geobiology