The diverse range of mechanisms driving the Arctic amplification are not completely understood and, moreover, the role of the greenhouse gas methane in Arctic warming remains unclear. Strong sources of methane at the ocean seabed in the Barents Sea and other polar regions are well documented. Nevertheless, those data suggest that negligible amounts of methane fluxed from the seabed enter the atmosphere, with roughly 90% of the methane consumed by bacteria. The observations are taken during summer, which is favorable for collecting data but also characterized by a strongly-stratified water column. In winter the stratification weakens and after a breakdown of the pycnocline, convection, storms, and turbulent diffusion can mix the full-depth water column in high latitudes.TheMixed Layer Depth (MLD) in the ice-free Central/Southern Barents Sea is deepening and the ocean-atmosphere methane exchange increases.. An additional barrier for the air-sea flux is seasonally and interannually variable sea-ice cover in partially ice-covered seas. We present Thermal IR space-based spectrometer data between 2002 and 2019 that shows increased methane concentration anomalies over the Barents and Kara seas in winter months. The seasonal methane cycle amplitude north of the Kara Sea has more than doubled since the beginning of the century; this may be interpreted as an effect of sea-ice decline and/or an evidence for growth of seabed emissions. A progressing degradation of Arctic sea-ice cover may lead to increased methane flux and, through a positive feedback loop, to further warming.

On decadal timescales, the greenhouse gas methane (CH4) is ~100 times more potent than carbon dioxide. Its abundance is increasing, many of its sources are temperature dependent. The Arctic is the site of the fastest warming globally. Feed-backs between Arctic temperature and CH4 emissions and concentrations need investigation. Unfortunately, available Arctic in situ data are extremely sparse with no marine observations outside summer. Satellite instruments measuring solar radiation reflected from the surface are ineffective in the Arctic. Thus, we leverage satellite data from AIRS, IASI-1, and IASI-2 Thermal Infrared (TIR) spectrometers, which provide year-round, day/night CH4 observations. Available in situ high latitude NOAA/ESRL surface coastal (50-85°N) flask atmospheric CH4 concentrations were compared with satellite data. We find: 1) remote sensing data revealed 150% (IASI-1, mid-upper troposphere) and 80% (surface data for Arctic stations) increases in atmospheric CH4 concentration growth rates between 2010-2014 and 2014-2017 time spans. Global NOAA/ESRL surface concentration rates increased by 90% for the same period; 2) maximum CH4 seasonal emission from the Arctic land occurs in boreal summer, while that from the Barents Kara Sea (BKS) occurs in boreal winter (Nov–Mar). Total annual Arctic Ocean CH4 emissions are preliminary estimated as ~40% of all land emissions North of 50°N; 3) marine emissions are concentrated in shelf areas within ~100 km of the coasts of major Arctic BKS lands; 4) CH4 anomalies over BKS, defined as surplus over its concentration at the North Atlantic area, grew after 2014; 5) the strongest SST increase was observed every year in the southeast Barents Sea in June due to strengthening of the warm Murman Currents and in the south Kara Sea in Sept. Direct in situ CH4 flux measurements during polar night over sea are necessary to test the satellite results.