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Strong methane point sources contribute a disproportionate fraction of total emissions across multiple basins in the United States
Authors:Daniel H. Cusworth  Andrew K. Thorpe  Alana K. Ayasse  David Stepp  Joseph Heckler  Gregory P. Asner  Charles E. Miller  Vineet Yadav  John W. Chapman  Michael L. Eastwood  Robert O. Green  Benjamin Hmiel  David R. Lyon  Riley M. Duren
Affiliation:aArizona Institutes for Resilience, University of Arizona, Tucson, AZ 85721;bCarbon Mapper, Pasadena, CA 91105;cJet Propulsion Laboratory, California Institute of Technology, Pasadena, CA 91109;dCenter for Global Discovery and Conservation Science, Arizona State University, Tempe, AZ 85281;eEnvironmental Defense Fund, Austin, TX 78701
Abstract:Understanding, prioritizing, and mitigating methane (CH4) emissions requires quantifying CH4 budgets from facility scales to regional scales with the ability to differentiate between source sectors. We deployed a tiered observing system for multiple basins in the United States (San Joaquin Valley, Uinta, Denver-Julesburg, Permian, Marcellus). We quantify strong point source emissions (>10 kg CH4 h−1) using airborne imaging spectrometers, attribute them to sectors, and assess their intermittency with multiple revisits. We compare these point source emissions to total basin CH4 fluxes derived from inversion of Sentinel-5p satellite CH4 observations. Across basins, point sources make up on average 40% of the regional flux. We sampled some basins several times across multiple months and years and find a distinct bimodal structure to emission timescales: the total point source budget is split nearly in half by short-lasting and long-lasting emission events. With the increasing airborne and satellite observing capabilities planned for the near future, tiered observing systems will more fully quantify and attribute CH4 emissions from facility to regional scales, which is needed to effectively and efficiently reduce methane emissions.

Due to its short atmospheric lifetime and strong contribution to global radiative forcing, methane (CH4) has been a focus for near-term climate mitigation efforts (1). Robust, unbiased accounting systems are requisite to prioritizing and validating CH4 mitigation, ideally from multiple independent data streams. Atmospheric observations of CH4 can be key for mitigation, as observed CH4 concentrations are used to quantify emission rates and attribute emissions to sources. Findings from many independent research efforts have shown that CH4 emissions across multiple sectors follow heavy-tailed distributions (25), meaning that a small fraction of emission sources emits at disproportionately higher rates than the full population of emitters. CH4 sources can be intermittent or persistent in duration, which may be associated with short-lasting process-driven releases or long-lasting emissions due to abnormal or otherwise avoidable operating conditions such as malfunctions or leaks (5). Isolating populations of large emitters at varying levels of intermittency while quantifying their contribution to regional budgets creates a clear direction for mitigation focus. This tiered observing system strategy can be deployed in data-rich regions where multiple independent layers of observations are jointly leveraged to quantify and isolate emissions, and then drive action.Advances in CH4 remote sensing have enabled quantification of emissions from global to facility scales. Generally, these observing systems operate by measuring solar backscattered radiance in shortwave infrared regions where CH4 is a known absorber. Global mapping satellite missions have been used to identify CH4 hotspots and infer global- to regional-scale CH4 emission fluxes (68). In particular, the TROPOspheric Monitoring Instrument [TROPOMI (9)] onboard the Sentinel-5p satellite has proven capable of quantifying fluxes at basin scales (10, 11). Due to the kilometer-scale resolution of measurements from these global mapping missions, further attribution to particular facilities or even emission sectors is often not feasible. Less precise, target-mode satellites [e.g., PRISMA (12), GHGSat (13)] have proven capable of quantifying very large emissions at an ∼30-m scale, allowing for direct emission attribution to facilities or even subfacility-level infrastructure. However, the current generation of CH4 plume imaging satellites lack the spatial and temporal coverage to provide quantification completeness across multiple basins. For global mapping, high–spatial resolution multispectral satellites such as Sentinel-2 and Landsat are capable of CH4 detection (14, 15), but only for large emission sources (e.g., 2+ t h−1) over very bright surfaces.Airborne imaging spectrometers with shortwave infrared sensitivities and sufficient instrument signal-to-noise ratios can also quantify column CH4 concentrations. These remote sensing platforms are capable of resolving CH4 concentrations at high spatial resolution (∼3 to 5 m) depending on flight altitude, and can quantify point source emissions as low as 5 to 10 kg h−1 (16, 17). These instruments are sensitive to concentrated point-source emissions, and less sensitive to diffuse emissions spread over large areas (e.g., wetlands). Given the heavy-tailed nature of anthropogenic emissions, point-source detections above an imaging spectrometer’s detection limit may constitute a sizable fraction of the total regional CH4 flux, but independent measurements are needed to provide that context. Therefore, in this study, we flew a combination of the Global Airborne Observatory (GAO) and next-generation Airborne Visible/Infrared Imaging Spectrometer (AVIRIS-NG) over multiple CH4 emitting regions between 2019 and 2021, including the southern San Joaquin Valley (SJV), the Permian, the Denver-Julesburg (DJ), the Unita, and the southwestern Pennsylvania portion of the Marcellus. We generally mapped each basin at least three times during each campaign to quantify persistence of emission sources. For the Permian, DJ, and SJV, we surveyed each region again after several months to assess trends and identify long-lasting emission sources. We also performed simultaneous regional CH4 flux inversions based on TROPOMI CH4 retrievals to quantify the total CH4 flux for each survey and compared against the quantified airborne point source budgets. With this tiered approach, we are able to quantify the contribution of unique point sources by sector on the regional budget, therefore highlighting specific points of action for mitigation.
Keywords:methane   fossil fuel   imaging spectroscopy   inversion   livestock
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