C33F-01
Methane release from the East Siberian Arctic Shelf: The role of subsea permafrost and other controlling factors as inferred from decadal observational and modeling efforts
Wednesday, 16 December 2015: 13:40
3007 (Moscone West)
Natalia E Shakhova, University of Alaska Fairbanks, Fairbanks, AK, United States; Tomsk Polytechnic University, Institute of Natural Resources, Tomsk, Russia and International Siberian Shelf Studies Team
Abstract:
Sustained methane (CH4) release from thawing Arctic permafrost to atmosphere may be a positive, major feedback to climate warming. East Siberian Arctic Shelf (ESAS) atmospheric CH4 venting was reported as on par with flux from Arctic tundra. Unlike release when ancient carbon in thawed on-land permafrost is mobilized, ESAS CH4 release is not determined by modern methanogenesis. Pre-formed CH4 largely stems from seabed deposits. Our investigation, including observational studies using hydrological, biogeochemical, geophysical, geo-electrical, microbiological, and isotopic methods, and modeling efforts to assess current subsea permafrost state and the ESAS’ contribution to the regional CH4 budget, have clarified processes driving ESAS CH4 emissions. Subsea permafrost state is a major emission determinant; rates vary by 3-5 orders of magnitude. Outer ESAS CH4 emission rates, where subsea permafrost is predicted to be degraded due to long submergence by seawater, in places are similar to near-shore rates, where deep/open taliks can form due to combined heating effects of seawater, river runoff, geothermal flux, and pre-existing thermokarst. Progressive subsea permafrost thawing and decreasing ice extent could significantly increase ESAS CH4 emissions. Subsea permafrost drilling results reveal modern recently submerged subsea permafrost degradation rates, contradicting previous hypotheses that thousands of years required to form escape paths for permafrost-preserved gas. We used a decadal observational ESAS water column and atmospheric boundary layer (ABL) data set to define the minimum source strength required to explain observed seasonally-increased ABL CH4 concentration. Modeling results agree with estimates from in-situ sonar data. In <10 m shallow water ≤72% of CH4 remains in surfacing bubbles. Dissolved CH4 fate largely depends on 3 factors: dissolved CH4 water column turnover time, water column stability against vertical mixing, and turbulent diffusion and lateral advection rates. Dissolved outer ESAS CH4 takes ≤1000 days to be oxidized because oxidation rates are low. Storms could release some aqueous CH4 to atmosphere; dissolved CH4, captured beneath ice in winter, can spread via currents and escape to atmosphere through breaks in the ice.