Attribution of the accelerating increase in atmospheric methane during 2010–2018 by inverse analysis of GOSAT observations

Author(s):  
Yuzhong Zhang ◽  
Daneil J. Jacob ◽  
Xiao Lu ◽  
Joannes D. Maasakkers ◽  
Tia R. Scarpelli ◽  
...  

<p>We conduct a global inverse analysis of 2010–2018 GOSAT satellite 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 4º×5º 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/gas), and too low for Venezuela (oil/gas) and the U.S. (oil/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 large production or use of fossil methane, including the U.S., 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.</p>

2021 ◽  
Vol 21 (5) ◽  
pp. 3643-3666 ◽  
Author(s):  
Yuzhong Zhang ◽  
Daniel J. Jacob ◽  
Xiao Lu ◽  
Joannes D. Maasakkers ◽  
Tia R. Scarpelli ◽  
...  

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.


2020 ◽  
Author(s):  
Yuzhong Zhang ◽  
Daniel J. Jacob ◽  
Xiao Lu ◽  
Joannes D. Maasakkers ◽  
Tia R. Scarpelli ◽  
...  

Abstract. We conduct a global inverse analysis of 2010–2018 GOSAT satellite observations to better understand the factors controlling atmospheric methane and its accelerating increase over the 2010–2018 period. The inversion optimizes 2010–2018 anthropogenic methane emissions and their trends on a 4º × 5º grid, monthly regional wetland emissions, and annual hemispheric concentrations of tropospheric OH (the main sink of methane) also for individual years. We use an analytical solution to the Bayesian optimization problem that provides closed-form estimates of error covariances and information content for the solution. Our inversion successfully reduces the errors against the independent methane observations from the TCCON network and 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/gas), and too low for Venezuela (oil/gas) and the U.S. (oil/gas). We show that the 2010–2018 increase in global methane emissions is mainly driven by tropical wetlands (Amazon and tropical Africa), boreal wetlands (Eurasia), and tropical livestock (South Asia, Africa, Brazil), with no significant trend in oil/gas emissions. While the rise in tropical livestock emissions is consistent with bottom-up estimates of rapidly growing cattle populations, the rise in wetland emissions needs to be better understood. The sustained acceleration of growth rates in 2016–2018 relative to 2010–2013 is mostly from wetlands, while the peak methane growth rates in 2014–2015 are also contributed by low OH concentrations (2014) and high fire emissions (2015). 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.


2019 ◽  
Author(s):  
Joannes D. Maasakkers ◽  
Daniel J. Jacob ◽  
Melissa P. Sulprizio ◽  
Tia R. Scarpelli ◽  
Hannah Nesser ◽  
...  

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 log-normal. Inversion results show large overestimates of Chinese coal emissions and Middle East oil/gas emissions in the EDGAR v4.3.2 inventory, but little error in the US where we use a new gridded version of the EPA national greenhouse gas inventory as prior estimate. Oil/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.


2020 ◽  
Author(s):  
Joannes D. Maasakkers ◽  
Daniel J. Jacob ◽  
Melissa P. Sulprizio ◽  
Tia R. Scarpelli ◽  
Hannah Nesser ◽  
...  

Abstract. We use 2010–2015 GOSAT satellite observations of atmospheric methane columns over North America in a high- resolution inversion of methane emissions, including contributions from different sectors and long-term trends. The inversion involves analytical solution to the Bayesian optimization problem for a Gaussian mixture model (GMM) of the emission field with up to 0.5° × 0.625° resolution in concentrated source regions. Analytical solution provides a closed-form characterization of the information content from the inversion and facilitates the construction of a large ensemble of solutions exploring the effect of different uncertainties and assumptions. Prior estimates for the inversion include a gridded version of the EPA Inventory of U.S. Greenhouse Gas Emissions and Sinks (GHGI) and the WetCHARTS model ensemble for wetlands. Our best estimate for mean 2010–2015 US anthropogenic emissions is 30.6 (range: 29.4–31.3) Tg a-1, slightly higher than the gridded EPA inventory (28.7 (26.4–36.2) Tg a-1). The main discrepancy is for the oil and gas production sectors where we find higher emissions than the GHGI by 35 % and 22 % respectively. The most recent version of the EPA GHGI revises downward its estimate of emissions from oil production and we find that these are a factor 2 lower than our estimate. Our best estimate of US wetland emissions is 10.2 (5.6–11.1) Tg a-1, on the low end of the prior WetCHARTS inventory uncertainty range (14.2 (3.3–32.4) Tg a-1) and calling for better understanding of these emissions. We find an increasing trend in US anthropogenic emissions over 2010–2015 of 0.4 % a-1, lower than previous GOSAT-based estimates but opposite to the decrease reported by the EPA GHGI. Most of this increase appears driven by unconventional oil/gas production in the eastern US. We also find that oil/gas production emissions in Mexico are higher than in the nationally reported inventory, though there is evidence for a 2010–2015 decrease in emissions from offshore oil production.


2021 ◽  
Author(s):  
Xiao Lu ◽  
Daniel J. Jacob ◽  
Haolin Wang ◽  
Joannes D. Maasakkers ◽  
Yuzhong Zhang ◽  
...  

Abstract. We quantify methane emissions and their 2010–2017 trends by sector in the contiguous United States (CONUS), Canada, and Mexico by inverse analysis of in situ (GLOBALVIEWplus CH4 ObsPack) and satellite (GOSAT) atmospheric methane observations. The inversion uses as prior estimate the national anthropogenic emission inventories for the three countries reported by the US Environmental Protection Agency (EPA), Environment and Climate Change Canada (ECCC), and the Instituto Nacional de Ecologia y Cambio Climatico (INECC) in Mexico to the United Nations Framework Convention on Climate Change (UNFCCC), and thus serves as an evaluation of these inventories in terms of their magnitudes and trends. Emissions are optimized with a Gaussian mixture model (GMM) at 0.5° × 0.625° resolution and for individual years. Optimization is done analytically using log-normal error forms. This yields closed-form statistics of error estimates and information content on the posterior (optimized) estimates, allows better representation of the high tail of the emission distribution, and enables construction of a large ensemble of inverse solutions using different observations and assumptions. We find that GOSAT and in situ observations are largely consistent and complementary in the optimization of methane emissions for North America. Mean 2010–2017 anthropogenic emissions from our base GOSAT + in situ inversion, with ranges from the inversion ensemble, are 36.9 (32.5–37.8) Tg a−1 for CONUS, 5.3 (3.6–5.7) Tg a−1 for Canada, and 6.0 (4.7–6.1) Tg a−1 for Mexico. These are higher than the most recent reported national inventories of 26.0 Tg a−1 for the US (EPA), 4.0 Tg a−1 for Canada (ECCC), and 5.0 Tg a−1 for Mexico (INECC). The correction in all three countries is largely driven by a factor of 2 underestimate in emissions from the oil sector with major contributions from the south-central US, western Canada, and southeast Mexico. Total CONUS anthropogenic emissions in our inversion peak in 2014, in contrast to the EPA report of a steady decreasing trend over 2010–2017. This reflects combined effects of increases in emissions from the oil and landfill sectors, decrease from the gas, and flat emissions from the livestock and coal sectors. We find decreasing trends in Canadian and Mexican anthropogenic methane emissions over the 2010–2017 period, mainly driven by oil and gas emissions. Our best estimates of mean 2010–2017 wetland emissions are 8.4 (6.4–10.6) Tg a−1 for CONUS, 9.9 (7.8–12.0) Tg a−1 for Canada, and 0.6 (0.4–0.6) Tg a−1 for Mexico. Wetland emissions in CONUS show an increasing trend of 2.6 (1.7–3.8) % a−1 over 2010–2017 correlated with precipitation.


2021 ◽  
Author(s):  
Tia R. Scarpelli ◽  
Daniel J. Jacob ◽  
Shayna Grossman ◽  
Xiao Lu ◽  
Zhen Qu ◽  
...  

Abstract. We present an updated version of the Global Fuel Exploitation Inventory (GFEI) for methane emissions and evaluate it with results from global inversions of atmospheric methane observations from satellite (GOSAT) and in situ platforms (GLOBALVIEWplus). GFEI allocates methane emissions from oil, gas, and coal sectors and subsectors to a 0.1° × 0.1° grid by using the national emissions reported by individual countries to the United Nations Framework Convention on Climate Change (UNFCCC) and mapping them to infrastructure locations. Our updated GFEI v2 gives annual emissions for 2010–2019 that incorporate the most recent UNFCCC national reports, new oil/gas well locations, and improved spatial distribution of emissions for Canada, Mexico, and China. Russia's oil/gas emissions decrease by 83 % in its latest UNFCCC report while Nigerian emissions increase sevenfold, reflecting changes in assumed emission factors. Global gas emissions in GFEI v2 show little net change from 2010 to 2019 while oil emissions decrease and coal emissions slightly increase. Global emissions in GFEI v2 are lower than the EDGAR v6 and IEA inventories for all sectors though there is considerable variability in the comparison for individual countries. GFEI v2 estimates higher emissions by country than the Climate TRACE inventory with notable exceptions in Russia, the US, and the Middle East. Inversion results using GFEI as a prior estimate confirm the lower Russian emissions in the latest UNFCCC report but Nigerian emissions are too high. Oil/gas emissions are generally underestimated by the national inventories for the highest emitting countries including the US, Venezuela, Uzbekistan, Canada, and Turkmenistan. Offshore emissions in GFEI tend to be overestimated. Our updated GFEI v2 provides a platform for future evaluation of national emission inventories reported to the UNFCCC using the newer generation of satellite instruments such as TROPOMI with improved coverage and spatial resolution. It responds to recent aspirations of the Intergovernmental Panel on Climate Change (IPCC) to integrate top-down and bottom-up information into the construction of national emission inventories.


2019 ◽  
Author(s):  
Jian He ◽  
Vaishali Naik ◽  
Larry W. Horowitz ◽  
Ed Dlugokencky ◽  
Kirk Thoning

Abstract. Changes in atmospheric methane abundance have implications for both chemistry and climate as methane is both a strong greenhouse gas and an important precursor for tropospheric ozone. A better understanding of the drivers of trends and variability in methane abundance over the recent past is therefore critical for building confidence in projections of future methane levels. In this work, the representation of methane in the atmospheric chemistry model AM4.1 is improved by optimizing total methane emissions (to an annual mean of 576 ± 32 Tg yr−1) to match surface observations over 1980–2017. The simulations with optimized global emissions are in general able to capture the observed global trend, variability, seasonal cycle, and latitudinal gradient of methane. Simulations with different emission adjustments suggest that increases in methane sources (mainly from energy and waste sectors) balanced by increases in methane sinks (mainly due to increases in OH levels) lead to methane stabilization (with an imbalance of 5 Tg yr−1) during 1999–2006, and that increases in methane sources combined with little change in sinks (despite small decreases in OH levels) during 2007–2012 lead to renewed methane growth (with an imbalance of 14 Tg yr−1 for 2007–2017). Compared to 1999–2006, both methane emissions and sinks are greater (by 31 Tg yr−1 and 22 Tg yr−1, respectively) during 2007–2017. Our results also indicate that the energy sector is more likely a major contributor to the methane renewed growth after 2006 than wetland, as increases in wetland emissions alone are not able to explain the renewed methane growth with constant anthropogenic emissions. In addition, a significant increase in wetland emissions would be required starting in 2006, if anthropogenic emissions declined, for wetland emissions to drive renewed growth in methane, which is a less likely scenario. Simulations with varying OH levels indicate that 1 % change in OH levels could lead to an annual mean of ~ 4 Tg yr−1 difference in the optimized emissions and 0.08 year difference in the estimated tropospheric methane lifetime. Continued increases in methane emissions along with decreases in tropospheric OH concentrations during 2008–2015 prolong methane lifetime and therefore amplify the response of methane concentrations to emission changes. Uncertainties still exist in the partitioning of emissions among individual sources and regions.


2021 ◽  
Author(s):  
Mengyao Liu ◽  
Ronald Van der A ◽  
Michiel Van Weele ◽  
Henk Eskes ◽  
Xiao Lu ◽  
...  

<p>The high-resolution Tropospheric Monitoring Instrument (TROPOMI) satellite observations of atmospheric methane offer a powerful tool to identify emission hot spots and quantify regional emissions. The divergence of horizontal fluxes of NO<sub>2</sub> has already been proven to be an efficient way to resolve and quantify high sources on a global scale. Since the lifetime of CH<sub>4</sub> is in the order of 10 years, the sinks can be ignored at the synoptic time scale which makes the divergence method even more applicable to CH<sub>4 </sub>than to short-lived NO<sub>2</sub>. <br>Because plumes of newly emitted CH<sub>4 </sub>disperse within the Planetary Boundary Layer (PBL), we first convert the satellite observed total column average (XCH<sub>4</sub>) to a regional enhancement of methane in the PBL (∆XCH<sub>4_PBL</sub>) by using the CAMS global methane background reanalysis fields above the PBL. These model fields represent the transport- and chemically-modulated large-scale distribution of methane. Secondly, the divergence of ∆XCH<sub>4_PBL</sub> is derived by the use of the wind speeds halfway within the PBL. Based on the divergence, methane emissions are estimated on a 0.25°× 0.25° grid. We tested our new method for Texas in the United States and quantified methane emissions from the well-known oil-gas fields in the Permian Basin, as well as from – less well quantitatively established – oil-gas fields located in southern coastal areas. <br>Compared to traditional inverse methods, our method is not restricted by an a priori emission inventory and so far unidentified local sources (i.e. emissions from livestock in feed yards) may be found. Due to its computational efficiency, the method might be applied in the near future globally on the current spatial resolution.</p>


2017 ◽  
Author(s):  
Jian-Xiong Sheng ◽  
Daniel J. Jacob ◽  
Alexander J. Turner ◽  
Joannes D. Maasakkers ◽  
Melissa P. Sulprizio ◽  
...  

Abstract. We use observations of boundary layer methane from the SEAC4RS aircraft campaign over the Southeast US in August–September 2013 to estimate methane emissions in that region through an inverse analysis with up to 0.25 ° x 0.3125 ° (25 x 25 km2) resolution and with full error characterization. The Southeast US accounts for about half of total US anthropogenic emissions according to the gridded EPA national inventory and also has extensive wetlands. Our inversion uses state-of-science emission inventories as prior estimates, including a gridded version of the anthropogenic EPA Greenhouse Gas Inventory and the mean of the WetCHARTs ensemble for wetlands. Inversion results are independently verified by comparison with surface (NOAA/ESRL) and column (TCCON) methane observations. Our posterior estimates for the Southeast US are 12.8 ± 0.9 Tg a−1 for anthropogenic sources (no significant change from the gridded EPA inventory) and 9.4 ± 0.8 Tg a−1 for wetlands (27 % decrease from the mean in the WetCHARTs ensemble). The largest source of error in the WetCHARTs wetlands ensemble is the landcover map specification of wetland areal extent. We find no regional bias in the anthropogenic EPA inventory, including for different source sectors, in contrast with previous inverse analyses that found the EPA inventory to be too low at national scales. These previous inversions relied on prior anthropogenic source patterns from the EDGAR v4.2 inventory that have considerable error, and also assumed low wetland emissions. Despite the regional-scale consistency, we find significant local errors in the EPA inventory for oil/gas production fields, suggesting that emission factors are more variable than assumed in the inventory.


2016 ◽  
Author(s):  
Michael Buchwitz ◽  
Oliver Schneising ◽  
Maximilian Reuter ◽  
Jens Heymann ◽  
Sven Krautwurst ◽  
...  

Abstract. Methane is an important atmospheric greenhouse gas and an adequate understanding of its emission sources is needed for climate change assessments, predictions and the development and verification of emission mitigation strategies. Satellite retrievals of near-surface-sensitive column-averaged dry-air mole fractions of atmospheric methane, i.e., XCH4, can be used to quantify methane emissions. Here we present a simple and fast method to estimate emissions of methane hotspots from satellite-derived XCH4 maps. We apply this method to an ensemble of XCH4 data products consisting of two products from SCIAMACHY/ENVISAT and two products from TANSO-FTS/GOSAT covering the time period 2003–2014. We obtain annual emissions of the source areas Four Corners in the southwestern USA, for the southern part of Central Valley, California, and for Azerbaijan and Turkmenistan. We find that our estimated emissions are in good agreement with independently derived estimates for Four Corners and Azerbaijan. For the Central Valley and Turkmenistan our estimated annual emissions are higher compared to the EDGAR v4.2 anthropogenic emission inventory. For Turkmenistan we find on average about 50 % higher emissions with our annual emission uncertainty estimates overlapping with the EDGAR emissions. For the region around Bakersfield in the Central Valley we find a factor of 6–9 higher emissions compared to EDGAR albeit with large uncertainty. Major methane emission sources in this region are oil/gas and livestock. Our findings corroborate recently published studies based on aircraft and satellite measurements and new bottom-up estimates reporting significantly underestimated methane emissions of oil/gas and/or livestock in this area in inventories.


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