Significance
Large methane point sources exist across multiple source sectors (e.g., oil, gas, coal, livestock, waste). Lacking is a robust assessment of the relative contribution of strong methane point sources against total or regional budgets, which is needed for prioritizing mitigation. In this study, we flew airborne imaging spectrometers repeatedly over multiple basins in the United States to quantify large methane point sources across multiple sectors. We compared these point sources to satellite-based regional flux inversions and found that methane super-emitters consistently make up a sizable contribution to total the total flux in a basin. These results show that a significant climate benefit can be realized by specific isolation and remediation of relatively few sources.
Keywords: methane, fossil fuel, imaging spectroscopy, inversion, livestock
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 (2–5), 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 (6–8). 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.
Results and Discussion
Point and Regional CH4 Budgets across Multiple Basins.
Fig. 1A shows the results from the multibasin surveys, including persistence-adjusted point source emissions (see Materials and Methods) compared against 1) total CH4 fluxes we derived simultaneously from a regularized inversion of TROPOMI XCH4 column concentrations (methods described in SI Appendix, Section S2.1) (18), and 2) bottom-up gridded emission inventories for oil and gas (O&G), other anthropogenic, and natural sources (19–21). Our CH4 flux inversion approach has been validated using independent flux estimates from multiple basins (SI Appendix, Section S2.2), and the gridded results for each inversion are shown in SI Appendix, Figs. S2–S4. All emission estimates are normalized to the area covered by each survey (Table 1). We find that across all basin and time periods, point sources make up on average 40% of each basin’s total flux. This occurs both in O&G-dominant basins (Permian, Uinta), but also in basins with more differentiated sources (Marcellus, DJ, SJV). In particular, in the surveyed area of the Marcellus basin, we ascribe 58% of the regional flux to point sources, which is driven primarily by persistent coal mine venting that makes up 65% of the point source budget. Venting is an expected and permitted operation, but is a major contributor to regional and national greenhouse gas emissions. The coal venting operations we quantified just in the southwestern portion of Pennsylvania together represent 0.36 ± 0.13 Tg a−1. This constitutes 1.3% of the US Environmental Protection Agency (EPA)’s national CH4 bottom-up inventory for 2019 (26.9 Tg) and 3.4% of the national energy sector emission estimates (10.7 Tg), which includes all fossil-fuel CH4 sources (22).
Table 1.
Basin | Dates surveyed | Area surveyed (km2) | No. of detected plumes | Total airborne CH4 emissions (t h−1)* |
Sector contribution to point source total (%)† | Average no. of overpasses per source | Average source persistence (unitless) | Total area CH4 flux (t h−1)‡ |
Contribution of point sources to area flux (%) |
---|---|---|---|---|---|---|---|---|---|
San Joaquin Valley | July 8 to September 24, 2020 | 5,600 | 284 | 10.6 ± 3.3 | O: 65 W: 2 M: 33 C: 0 |
8.2 | 0.29 | 22.5 ± 3.3 | 47 |
San Joaquin Valley | November 9–23, 2020 | 5,600 | 111 | 5.56 ± 2.0 | O: 100 W: 0 M: 0 C: 0 |
6.2 | 0.28 | 22.2 ± 4.5 | 25 |
San Joaquin Valley | November 5–13, 2021 | 5,600 | 68 | 2.34 ± 3.3 | O: 93 W: 0 M: 7 C: 0 |
3.1 | 0.41 | 17.6 ± 2.4 | 13 |
Permian | September 22 to November 4, 2019 | 54,000 | 3025 | 246 ± 79 | O: 100 W: 0 M: 0 C: 0 |
7.7 | 0.26 | 415 ± 110 | 59 |
Permian | July 13–24, 2020 | 8,400 | 595 | 72.3 ± 20 | O: 100 W: 0 M: 0 C: 0% |
3.2 | 0.45 | 177 ± 59 | 41 |
Permian | July 26 to August 10, 2021 | 8,900 | 901 | 67.7 ± 19 | O: 100 W: 0 M: 0 C: 0 |
3.9 | 0.39 | 181 ± 40 | 38 |
Permian | October 3–17, 2021 | 8,900 | 765 | 74.1 ± 27 | O: 100 W: 0 M: 0 C: 0 |
4.0 | 0.38 | 111 ± 28 | 67 |
Uinta | July 26 to August 7, 2020 | 6,200 | 123 | 6.13 ± 2.8 | O: 100 W: 0 M: 0 C: 0 |
3.6 | 0.44 | 33.9 ± 5.5 | 18 |
Denver-Julesburg | July 12–22, 2021 | 4,800 | 92 | 4.98 ± 2.1 | O: 50 W: 6 M: 44 C: 0 |
4.5 | 0.34 | 21.1 ± 4.1 | 24 |
Denver-Julesburg | September 19–29, 2021 | 4,800 | 94 | 5.37 ± 1.7 | O: 79 W: 5 M: 16 C: 0 |
4.8 | 0.28 | 25.2 ± 6.8 | 21 |
Southwest Pennsylvania | May 13–21, 2021 | 10,300 | 136 | 63.8 ± 24 | O: 33 W: 1 M: 0 C: 66 |
3.1 | 0.60 | 109 ± 39 | 59 |
*Total airborne emissions calculated by aggregated persistence-averaged source emissions within each observing domain.
†O, O&G; W, waste management; M, wet manure management; C, coal.
‡Total area flux estimated through inversion of TROPOMI XCH4 (methods described in SI Appendix, Section S2).
Fig. 1A shows that the bottom-up inventory generally underestimates the total CH4 flux derived from TROPOMI, a result consistent with previous top-down analyses (23). This discrepancy is due to several factors, including the age of the inventory (2012 to 2016) which may underestimate current activity information and emission factors, especially for O&G basins with increasing production (e.g., the Permian). Geospatial information included in the inventory may also be inaccurate or outdated, which biases comparisons to surveys that only look at subregions of full basins. However, Fig. 1C shows the relative contribution of O&G, waste, manure management, and coal emissions in each region, as quantified by our airborne surveys and the bottom-up inventory. Here, relative contributions are more consistent with the bottom-up inventory across campaigns. A few caveats apply, especially in regard to manure management. For example, during the July 2021 DJ survey, the contributions from point source manure emissions (44%; 2,200 ± 970 kg h−1) were nearly equal to O&G emissions (50%; 2,490 ± 1,100 kg h−1). When the basin was resurveyed in September to October 2021, the contribution from manure was only 875 ± 280 kg h−1 or 16% of the total (5,370 ± 1,700 kg h−1), due to both a reduction in manure emissions and an increase in O&G emissions (79%; 4,250 ± 1,400 kg h−1). The bottom-up inventory estimates only 6.5% of emissions from manure in this same region, an underestimate compared to either airborne DJ survey. According to measurements from the Greely Airport (24), the average local noontime temperature dropped 5°C between summer and fall campaigns. More study is needed to verify if seasonal variability can explain the apparent discrepancy with the bottom-up inventory or if manure management is a much larger relative emitter than expected.
Table 2 lists observed O&G point sources by upstream and midstream supply-chain segments, including production site (well site or tank battery at well site), pipeline (mostly gathering with some transmission), compression (gathering and transmission), processing plants, and other or unidentifiable O&G infrastructure. For every survey, production makes up the majority of the O&G emission budget, although its contribution is highly variable, ranging from 39 to 82%. Compression and processing make up a smaller percentage of the budget (7.1 to 35% and 0 to 11%, respectively), which is consistent with top-down studies (23). One discrepancy is in the Permian Basin, where compression and processing represent 19 to 35% and 6 to 11% of the O&G budget, respectively. The higher concentration of emissions in the midstream sector in the Permian is a result observed previously and is likely the result of insufficient haul-away capacity to match the fast increase in production in the basin (5, 25).
Table 2.
Basin | Dates surveyed | O&G point source total (t h−1) |
Production (%) | Compression (%) | Gathering pipelines (%) | Processing (%) | Other (%) |
---|---|---|---|---|---|---|---|
San Joaquin Valley | July 8 to September 24, 2020 | 6.92 ± 2.1 | 43 | 7 | 45 | 0 | 5 |
San Joaquin Valley | November 9–23, 2020 | 5.56 ± 2.0 | 39 | 16 | 41 | 2 | 2 |
San Joaquin Valley | November 5–13, 2021 | 2.17 ± 1.0 | 66 | 11 | 23 | 0 | 0 |
Permian | September 22 to November 4, 2019 | 246 ± 79 | 50 | 19 | 23 | 9 | 0 |
Permian | July 13–24, 2020 | 72.3 ± 20 | 39 | 35 | 20 | 6 | 0 |
Permian | July 26 to August 10, 2021 | 67.7 ± 19 | 43 | 31 | 19 | 7 | 0 |
Permian | October 3–17, 2021 | 74.1 ± 27 | 47 | 33 | 9 | 11 | 1 |
Uinta | July 26 to August 7, 2020 | 6.13 ± 2.8 | 59 | 2 | 34 | 5 | 0 |
Denver-Julesburg | July 12–22, 2021 | 2.54 ± 1.1 | 71 | 12 | 7 | 9 | |
Denver-Julesburg | September 19–29, 2021 | 4.25 ± 1.4 | 51 | 13 | 28 | 9 | 0 |
Southwest Pennsylvania | May 13–21, 2021 | 20.9 ± 7.8 | 82 | 15 | 3 | 0 | 0 |
Average across campaigns | 53 | 18 | 23 | 5 | 1 |
Timescales of Short- and Long-Lasting Emission Sources.
In Fig. 1, we use frequency of plume detections (i.e., persistence) to calculate time-averaged emission rates at each source location. A related metric is the timescale of each emission source for sources where multiple plumes were detected across independent flight days. We define source timescale as the length of time between the first and the last plume detection for a given source. In order to compare across multiple campaigns, we normalize timescales by the length of their respective campaign or campaigns. For example, if the timescale of a source is 6 d for a 10-d campaign, then the normalized timescale is 0.6. Due to revisit feasibility during field campaigns, not every source can be flown on the first and last days of each campaign, so this normalization may artificially shorten timescales. However, this potential source of bias becomes negligible when looking at field campaigns across multiple months and years.
Fig. 2 shows the distribution of emission source timescales for individual campaigns. The distribution of timescales for individual campaigns (Fig. 2A) is nearly flat, but shows a slight decrease as timescales get longer, except for a small jump around 0.8, due to persistent coal venting emissions in the Marcellus (Table 1). This overall flat structure is likely due to sampling conditions during individual campaigns; uniform revisit frequency for sources within campaigns is often technically infeasible given weather and other logistical considerations. Therefore, we also calculate source timescales for multimonth (DJ summer/fall 2021; Permian summer/fall 2021; SJV summer/fall 2020) and multiyear campaigns (Permian 2019 to 2021; SJV 2020 to 2021) by reclustering plumes to emission sources across the longer multimonth or year temporal domain (Fig. 2 B and C). For multimonth campaigns, a clear bimodal structure appears centered around short timescales (0 to 0.2) and long timescales (0.7 to 1.0). The bimodal structure persists for multiyear campaigns (Permian 2019 to 2021; SJV 2020 to 2021), showing that some sources show sustained emission activity over long timescales.
Sources with both short and long timescales contribute significant fractions to total emissions. Fig. 2D shows the cumulative contribution of emissions from each normalized timescale bin to the total. For multimonth and year campaigns, sources with normalized timescales greater than 0.7 contribute 38 to 39% to the total. Short-lasting sources (0 to 0.3 normalized timescale) contribute 41 to 48% to the total. For effective mitigation, this means that within the point source population of emissions, top-down monitoring solutions need temporal sampling capability to capture both source timescales. Long-lasting sources may be indicative of leaks, malfunctions, or some known releases (e.g., permitted coal venting). Short-lasting sources may be indicative of expected releases (e.g., temporary maintenance) or malfunctions triggered by variable process conditions (e.g., pressure buildup). A revisit strategy with long revisit intervals (e.g., months) would not be able to easily distinguish between these timescale categories and could potentially miss a sizable contribution from short-lasting emission sources.
Emission Trends.
The multiyear campaigns in the Permian and SJV allow us to look at basin-scale trends. In the Permian, the spatial overflight domains across campaigns are not consistent. The fall 2019 campaign mapped a much wider area of the Permian, and subsequent campaigns in 2020 to 2021 focused on areas of large activity that were originally identified in 2019. We therefore look at just the overlapping regions flown among all campaigns. Within the region of overlap (SI Appendix, Fig. S5), the point-source aggregated emissions from 2019 are much higher (0.84 ± 0.27 Tg a−1) than in subsequent revisits in summer 2020, summer 2021, and fall 2021 (0.52 ± 0.15 Tg a−1, 0.41 ± 0.12 Tg a−1, and 0.48 ± 0.19 Tg a−1, respectively). Reduction from high fall 2019 CH4 emissions, quantified by both airborne and satellite data, may be due to multiple causes. COVID-19 and oil market impacts were previously observed to correlate with reduced flaring activity and fewer well completions, which can impact CH4 emissions (25). In addition, since 2019, aerial and ground-based data generated from this and other studies have been shared with operators on an ongoing basis (e.g., via PermianMap.org). Other operators have funded independent aerial measurements and have claimed emission reductions based on those results [e.g., ExxonMobil (26)]. Another cause could be the heterogeneity of operators, leases, and supply chain activity in the Permian contributing to general high variability in emissions. For example, fall 2019 aggregated Permian airborne point-source emissions were as much as a factor of 2 variable on daily to weekly timescales (5). More long-term trend and attribution analysis is needed to disentangle trends from general variability for the Permian.
A strong relative reduction (69 to 76%) in point-source emissions occurred in SJV between summer 2020 and fall 2021, along with a 20% reduction in the total flux (Table 1). This also corresponds to an 81% emission reduction for point sources in SJV observed with AVIRIS-NG during the California Methane Survey (12,600 ± 3,700 kg h−1) (4). The decrease in emissions is driven by reductions in both the O&G and livestock sectors. Since 2016, many digesters (impermeable liners) were placed over manure lagoons across multiple dairies in southern Kern County (27). This appears to have had a sizable impact, as emissions from this sector reduced in summer 2021 from 3,500 ± 1,100 kg h−1 to 166 ± 77 kg h−1 in 2021. There was not complete overlap in these regions across campaigns, and dairies were not sampled during the fall 2020 campaign. However, almost all manure CH4 sources detected in summer 2020 were reflown in fall 2021. This indicates that the trend is not biased from sampling, although there could be a contribution from seasonality of emissions, which may also be driving manure emission variability in the DJ basin. O&G emissions dropped from 6,920 to 5,560 kg h−1 between summer and fall 2020 campaigns to 2,170 ± 1,000 kg h−1 in 2021. During the fall 2020 campaign, researchers from the California Air Resources Board, Carbon Mapper, and NASA JPL shared CH4 plume detections with individual operators and solicited feedback regarding causes of emissions and any mitigation efforts. Reductions in emissions between 2020 and 2021 could be driven by this outreach effort, although sustained monitoring is needed to confirm that sources remain low or nonemitting into the future.
Conclusions
No single instrument, measurement platform, or network is capable of full characterization of CH4 emissions within a basin or region. Therefore, tiered observing systems are needed to adequately constrain emission budgets and prioritize areas and infrastructure for mitigation. We demonstrated an application of this system using remote sensing platforms across multiple basins in the United States during 2019 to 2021. The results from this multibasin tiered analysis show that point sources make up around 40% of the total CH4 flux (13 to 67% range) and highlight the heavy-tailed nature of point sources across many regions and sectors. It is likely that if a basin is known to be made of up of any combination of emission sectors that are characteristically heavy tailed (e.g., O&G, coal, manure management, waste), there is a strong likelihood that point sources will make up a significant fraction of the entire region’s emissions.
We show that sources that emit over short and long timescales equally contribute to point source budgets, which has implications for designing monitoring strategies. Therefore, the global scalability of tiered observing systems depends on the completeness of atmospheric observations, which entails sensitivity to emissions, temporal revisit, and spatial completeness (28). In addition to aircraft campaigns, point-source quantification will rapidly expand with emerging satellite missions (e.g., Carbon Mapper; 2023 launch). Total basin flux estimation will also improve with wide-swath mapping missions (e.g., MethaneSat; 2023 launch). Where available, ground-based networks are also critical for quantifying regional emissions (29) and for validation of remote-sensing platforms. As these data products are refined and made freely available to the public in easily interpretable formats, there exists great potential in handing off atmospherically informed datasets to appropriate operators and agencies to ultimately reduce CH4 emissions.
Materials and Methods
Detailed descriptions of plume-level quality control protocols and TROPOMI flux algorithms and validation are described in the SI Appendix. Survey design and plume aggregation methods are described below.
Survey Design.
We mapped five distinct basins using GAO and/or AVIRIS-NG from 2019 to 2021 (Fig. 3). AVIRIS-NG and GAO are similarly built instruments that measure solar backscatter between 380 and 2,500 nm at 5-nm spectral resolution. CH4 concentrations were retrieved in the 2,200 to 2,400 nm CH4-absorbing region using a column-wise matched filter algorithm (5). Plumes were identified by visual inspection, whose protocols are described in the SI Appendix, Section S1. Emission rates and uncertainties were quantified using an integrated methane enhancement (IME) algorithm that has been validated against multiple controlled release experiments and independent in situ measurement (4, 16, 17). Fig. 3 shows example plumes that were detected across multiple basins and across unique sectors. Emission sectors with point source plume characteristics detectable by AVIRIS-NG/GAO include O&G, wet manure management from animal feedlots, waste management from high-capacity landfills, and coal mine seepage/venting. Other diffuse emissions, including enteric fermentation, dry manure management, and wetlands, are not easily detectable with this type of imaging spectrometer. Table 1 provides summary information for each basin, including dates and area flown, number of detected plumes, and estimated emissions. SI Appendix, Fig. S1 shows each domain and the specific flight line outlines for each survey.
Source Aggregation and Persistence Calculations.
To generate aggregate statistics for plumes that originate from the same facilities, each quantified plume is clustered in space and time with any other detection within 150 m, a typical lateral distance of a well site that is also within the geolocation uncertainty of the instrument (6 to 10 m). This process clusters plumes into sources, which can be attributed to facilities or infrastructure. GAO has a boresighted high-resolution (∼0.6 m) digital airborne camera that we use to attribute sources to specific sectors. For AVIRIS-NG, we use a combination of 3- to 5-m RGB (red, green, blue) channels from the imaging spectrometer and Google Earth base imagery for source attribution. For sources with at least three overflights, we apply persistence weighting to estimate average emissions. This weighting scales the average emission rate by persistence (f), or by the number of detections (M) divided by N, the number of overflights (f = M/N). We consider three overflights to be the minimum needed to detect a characteristically intermittent source; previous work found that the average intermittency of O&G emissions in California was f = 0.23 (4). Therefore, to have a greater than 50% probability of detecting emissions at that characteristic source, at least three overpasses are needed: p = 1 − (1 − 0.23)3 > 0.5. When aggregating emissions for a survey, we sum persistence-weighted source emissions. If there exist sources with less than three overflights in a survey, we sample the distribution of f values for that sector for that survey and assign it to that under-flown source before aggregating. To account for variability in sampling on aggregate emissions, we generate 1,000 Monte Carlo samples for each under-flown source for each survey.
Supplementary Material
Acknowledgments
Funding for flight operations and/or data analysis referenced in this paper was supported by NASA’s Carbon Monitoring System and Advanced Information System Technology programs as well as Rocky Mountain Institute, Environmental Defense Fund (EDF), California Air Resources Board (CARB), and the University of Arizona. Funding for Colorado overflights was provided by the Mark Martinez and Joey Irwin Memorial Public Projects Fund with the support of the Colorado Oil and Gas Conservation Commission and the Colorado Department of Public Health and Environment (CDPHE). The Carbon Mapper team also acknowledges the support of their sponsors including the High Tide Foundation, Bloomberg Philanthropies, Grantham Foundation, and other philanthropic donors. We thank colleagues at CARB, CDPHE, Colorado State University, University of Utah, EDF, and Pennsylvania Department of Environmental Protection for input on survey design and analysis for the California, Colorado, Utah, Permian, and Pennsylvania studies, respectively. Portions of this work were carried out at the Jet Propulsion Laboratory, California Institute of Technology, under a contract with the National Aeronautics and Space Administration (80NM0018D0004). We thank Dan Zimmerle for on-the-ground insights during the Denver-Julesburg flights. We thank Daniel Varon for conversations regarding inversion frameworks and validation. The Global Airborne Observatory (GAO) is managed by the Center for Global Discovery and Conservation Science at Arizona State University. The GAO is made possible by support from private foundations, visionary individuals, and Arizona State University.
Footnotes
The authors declare no competing interest.
This article is a PNAS Direct Submission. V.R. is a Guest Editor invited by the Editorial Board.
This article contains supporting information online at https://www.pnas.org/lookup/suppl/doi:10.1073/pnas.2202338119/-/DCSupplemental.
Data, Materials, and Software Availability
Emissions data have been deposited in Zenodo (https://doi.org/10.5281/zenodo.5606120) (30, 31). Emission data and plume images can also be visualized and downloaded via the Carbon Mapper open data portal at https://data.carbonmapper.org.
Change History
October 12, 2022: The term “Denver-Julesburg” has been updated in Figure 3 and the SI Appendix to correct a typographical error.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
Emissions data have been deposited in Zenodo (https://doi.org/10.5281/zenodo.5606120) (30, 31). Emission data and plume images can also be visualized and downloaded via the Carbon Mapper open data portal at https://data.carbonmapper.org.