B13G-0264:
Process-Level Measurements of Methane Production, Oxidation, and Efflux Across Geomorphic Gradients in Arctic Polygon Tundra
Monday, 15 December 2014
Lydia J Smith1,2, Mark E Conrad2, Margaret S Torn1,2, Markus Bill2, John Bryan Curtis2, Oriana Chafe2 and Melanie S Hahn1, (1)University of California Berkeley, Berkeley, CA, United States, (2)Lawrence Berkeley National Laboratory, Berkeley, CA, United States
Abstract:
Arctic wetlands are currently net sources of atmospheric CH4. CH4 emissions in Arctic tundra vary widely in space and time, with proximate controls—competing decomposition processes, substrate availability, CH4 oxidation, and CH4 transport—dependent on local climate, soil, hydrology, and biology. These complex controls and high spatial and temporal variability make it difficult to characterize current CH4 processes and predict their responses to climate change. We ask: (1) how do metabolic CH4 production pathways and oxidation rates vary across spatial and temporal gradients in the Arctic, and (2) how do these subsurface processes relate to surface greenhouse gas fluxes? In polygonal tundra in Barrow, Alaska, we sampled from a gradient of topographic features and subsurface ice properties, from areas with large, intact ice wedges and ice-rich permafrost (low polygons) and areas with smaller, degraded ice wedges and lower permafrost ice contents (flat/high polygons). 5 times in 2012 and 2013, we measured surface CH4 and CO2 fluxes, soil pore space concentrations of CH4, DIC, and N2O at 3 depths, stable isotope abundances of CH4 and DIC, and soil moisture and temperature. We find that surface greenhouse gas fluxes and CH4 production pathways vary between geomorphic features. Low polygons have high CH4 fluxes (~200 nm/m2s) and carbon isotope compositions typical of acetate cleavage, and flat/high polygons have low or negative CH4 fluxes and isotopic signatures typical of CO2 reduction. High dissolved CH4 concentrations at depth and 13C enrichment of shallow CH4 suggest CH4 oxidation controls surface efflux in upland features, while dual isotope measurements (D/H and 13C/ 12C) indicate shifting CH4 production pathways with depth, with acetate cleavage more important at shallower depths. Among distinct sub-features within each polygon type, we find that CH4 processes, relative oxidation rates, and surface emissions depend on subsurface ice properties in ways that cannot be explained by surface soil moisture and temperature measurements alone. As part of the Next Generation Ecosystem Experiment (NGEE-Arctic), this study’s results will be integrated with a broad range of measurements, with the goal of improving regional-scale models.