Abstract. We use 2010–2015 observations of atmospheric methane columns from the GOSAT satellite instrument in a global inverse analysis to improve estimates of methane emissions and their trends over the period, as well as the global concentration of tropospheric OH (the hydroxyl radical, methane's main sink) and its trend. Our inversion solves the Bayesian optimization problem analytically including closed-form characterization of errors. This allows us to (1) quantify the information content from the inversion towards optimizing methane emissions and its trends, (2) diagnose error correlations between constraints on emissions and OH concentrations, and (3) generate a large ensemble of solutions testing different assumptions in the inversion. We show how the analytical approach can be used, even when prior error standard deviation distributions are lognormal. Inversion results show large overestimates of Chinese coal emissions and Middle East oil and gas emissions in the EDGAR v4.3.2 inventory but little error in the United States where we use a new gridded version of the EPA national greenhouse gas inventory as prior estimate. Oil and gas emissions in the EDGAR v4.3.2 inventory show large differences with national totals reported to the United Nations Framework Convention on Climate Change (UNFCCC), and our inversion is generally more consistent with the UNFCCC data. The observed 2010–2015 growth in atmospheric methane is attributed mostly to an increase in emissions from India, China, and areas with large tropical wetlands. The contribution from OH trends is small in comparison. We find that the inversion provides strong independent constraints on global methane emissions (546 Tg a−1) and global mean OH concentrations (atmospheric methane lifetime against oxidation by tropospheric OH of 10.8±0.4 years), indicating that satellite observations of atmospheric methane could provide a proxy for OH concentrations in the future.

Rapid identification of anomalous methane sources in oil/gas fields could enable corrective action to fight climate change. The GHGSat‐D satellite instrument measuring atmospheric methane with 50‐meter spatial resolution was launched in 2016 to demonstrate space‐based monitoring of methane point sources. Here we report the GHGSat‐D discovery of an anomalously large, persistent methane source (10–43 metric tons per hour, detected in over 50% of observations) at a gas compressor station in Central Asia, together with additional sources (4–32 metric tons per hour) nearby. The TROPOMI satellite instrument confirms the magnitude of these large emissions going back to at least November 2017. We estimate that these sources released 142 ± 34 metric kilotons of methane to the atmosphere from February 2018 through January 2019, comparable to the 4‐month total emission from the well‐documented Aliso Canyon blowout.

Abstract. Individual countries report national emissions of methane, a potent greenhouse gas, in accordance with the United Nations Framework Convention on Climate Change (UNFCCC). We present a global inventory of methane emissions from oil, gas, and coal exploitation that spatially allocates the national emissions reported to the UNFCCC (Scarpelli et al., 2019). Our inventory is at 0.1∘×0.1∘ resolution and resolves the subsectors of oil and gas exploitation, from upstream to downstream, and the different emission processes (leakage, venting, flaring). Global emissions for 2016 are 41.5 Tg a−1 for oil, 24.4 Tg a−1 for gas, and 31.3 Tg a−1 for coal. An array of databases is used to spatially allocate national emissions to infrastructure, including wells, pipelines, oil refineries, gas processing plants, gas compressor stations, gas storage facilities, and coal mines. Gridded error estimates are provided in normal and lognormal forms based on emission factor uncertainties from the IPCC. Our inventory shows large differences with the EDGAR v4.3.2 global gridded inventory both at the national scale and in finer-scale spatial allocation. It shows good agreement with the gridded version of the United Kingdom's National Atmospheric Emissions Inventory (NAEI). There are significant errors on the 0.1∘×0.1∘ grid associated with the location and magnitude of large point sources, but these are smoothed out when averaging the inventory over a coarser grid. Use of our inventory as prior estimate in inverse analyses of atmospheric methane observations allows investigation of individual subsector contributions and can serve policy needs by evaluating the national emissions totals reported to the UNFCCC. Gridded data sets can be accessed at https://doi.org/10.7910/DVN/HH4EUM (Scarpelli et al., 2019).

Abstract. We conduct a global inverse analysis of 2010–2018 GOSAT observations to better understand the factors controlling atmospheric methane and its accelerating increase over the 2010–2018 period. The inversion optimizes anthropogenic methane emissions and their 2010–2018 trends on a 4∘×5∘ grid, monthly regional wetland emissions, and annual hemispheric concentrations of tropospheric OH (the main sink of methane). We use an analytical solution to the Bayesian optimization problem that provides closed-form estimates of error covariances and information content for the solution. We verify our inversion results with independent methane observations from the TCCON and NOAA networks. Our inversion successfully reproduces the interannual variability of the methane growth rate inferred from NOAA background sites. We find that prior estimates of fuel-related emissions reported by individual countries to the United Nations are too high for China (coal) and Russia (oil and gas) and too low for Venezuela (oil and gas) and the US (oil and gas). We show large 2010–2018 increases in anthropogenic methane emissions over South Asia, tropical Africa, and Brazil, coincident with rapidly growing livestock populations in these regions. We do not find a significant trend in anthropogenic emissions over regions with high rates of production or use of fossil methane, including the US, Russia, and Europe. Our results indicate that the peak methane growth rates in 2014–2015 are driven by low OH concentrations (2014) and high fire emissions (2015), while strong emissions from tropical (Amazon and tropical Africa) and boreal (Eurasia) wetlands combined with increasing anthropogenic emissions drive high growth rates in 2016–2018. Our best estimate is that OH did not contribute significantly to the 2010–2018 methane trend other than the 2014 spike, though error correlation with global anthropogenic emissions limits confidence in this result.