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We analyze present-day and future carbon monoxide (CO) simulations in 26 state-of-the-art atmospheric chemistry models run to study future air quality and climate change. In comparison with near-global satellite observations from the MOPITT instrument and local surface measurements, the models show large underestimates of Northern Hemisphere (NH) extratropical CO, while typically performing reasonably well elsewhere. The results suggest that year-round emissions, probably from fossil fuel burning in east Asia and seasonal biomass burning emissions in south-central Africa, are greatly underestimated in current inventories such as IIASA and EDGAR3.2. Variability among models is large, likely resulting primarily from intermodel differences in representations and emissions of nonmethane volatile organic compounds (NMVOCs) and in hydrologic cycles, which affect OH and soluble hydrocarbon intermediates. Global mean projections of the 2030 CO response to emissions changes are quite robust. Global mean midtropospheric (500 hPa) CO increases by 12.6 ± 3.5 ppbv (16%) for the high-emissions (A2) scenario, by 1.7 ± 1.8 ppbv (2%) for the midrange (CLE) scenario, and decreases by 8.1 ± 2.3 ppbv (11%) for the low-emissions (MFR) scenario. Projected 2030 climate changes decrease global 500 hPa CO by 1.4 ± 1.4 ppbv. Local changes can be much larger. In response to climate change, substantial effects are seen in the tropics, but intermodel variability is quite large. The regional CO responses to emissions changes are robust across models, however. These range from decreases of 10–20 ppbv over much of the industrialized NH for the CLE scenario to CO increases worldwide and year-round under A2, with the largest changes over central Africa (20–30 ppbv), southern Brazil (20–35 ppbv) and south and east Asia (30–70 ppbv). The trajectory of future emissions thus has the potential to profoundly affect air quality over most of the world's populated areas.

We present a systematic comparison of tropospheric NO2 from 17 global atmospheric chemistry models with three state-of-the-art retrievals from the Global Ozone Monitoring Experiment (GOME) for the year 2000. The models used constant anthropogenic emissions from IIASA/EDGAR3.2 and monthly emissions from biomass burning based on the 1997–2002 average carbon emissions from the Global Fire Emissions Database (GFED). Model output is analyzed at 10:30 local time, close to the overpass time of the ERS-2 satellite, and collocated with the measurements to account for sampling biases due to incomplete spatiotemporal coverage of the instrument. We assessed the importance of different contributions to the sampling bias: correlations on seasonal time scale give rise to a positive bias of 30–50% in the retrieved annual means over regions dominated by emissions from biomass burning. Over the industrial regions of the eastern United States, Europe and eastern China the retrieved annual means have a negative bias with significant contributions (between –25% and +10% of the NO2 column) resulting from correlations on time scales from a day to a month. We present global maps of modeled and retrieved annual mean NO2 column densities, together with the corresponding ensemble means and standard deviations for models and retrievals. The spatial correlation between the individual models and retrievals are high, typically in the range 0.81–0.93 after smoothing the data to a common resolution. On average the models underestimate the retrievals in industrial regions, especially over eastern China and over the Highveld region of South Africa, and overestimate the retrievals in regions dominated by biomass burning during the dry season. The discrepancy over South America south of the Amazon disappears when we use the GFED emissions specific to the year 2000. The seasonal cycle is analyzed in detail for eight different continental regions. Over regions dominated by biomass burning, the timing of the seasonal cycle is generally well reproduced by the models. However, over Central Africa south of the Equator the models peak one to two months earlier than the retrievals. We further evaluate a recent proposal to reduce the NOx emission factors for savanna fires by 40% and find that this leads to an improvement of the amplitude of the seasonal cycle over the biomass burning regions of Northern and Central Africa. In these regions the models tend to underestimate the retrievals during the wet season, suggesting that the soil emissions are higher than assumed in the models. In general, the discrepancies between models and retrievals cannot be explained by a priori profile assumptions made in the retrievals, neither by diurnal variations in anthropogenic emissions, which lead to a marginal reduction of the NO2 abundance at 10:30 local time (by 2.5–4.1% over Europe). Overall, there are significant differences among the various models and, in particular, among the three retrievals. The discrepancies among the retrievals (10–50% in the annual mean over polluted regions) indicate that the previously estimated retrieval uncertainties have a large systematic component. Our findings imply that top-down estimations of NOx emissions from satellite retrievals of tropospheric NO2 are strongly dependent on the choice of model and retrieval.

We have analyzed Sentinel‐5 Precursor TROPOspheric Monitoring Instrument (TROPOMI) data over the Copperbelt mining region (Democratic Republic of Congo and Zambia). Despite high background values, annual 2019–2022 means of TROPOMI NO2 (nitrogen dioxide) show local enhancements consistent with six point sources (four copper/cobalt mines, two cities) where high‐emission industrial activities take place. We have quantified annual NOx (nitrogen oxides) emissions from these point sources, identified temporal trends in emissions, and found strong correlations with production data from colocated mines and one oil refinery. The Copernicus Atmosphere Monitoring Service Global Anthropogenic (CAMS‐GLOB‐ANT) version 5 inventory underpredicts TROPOMI‐derived emissions and lacks the temporal trends observed in TROPOMI and mine/refinery production. These results demonstrate the potential for satellite monitoring of mining and other industrial activities, often unreported or underestimated, which impact the air quality of local communities. This is particularly important for Africa, where mining is increasing aggressively. Plain Language Summary: We show for the first time that annual NOx gas pollution emitted by individual copper/cobalt mines can be measured with TROPOMI satellite data, even in the presence of high background pollution from biomass burning and other sources. This is important for monitoring the air quality of local communities, particularly when these industrial activities proliferate in close proximity to population centers (as is the case in the Copperbelt mining region and in other African regions) and without sufficient ground measurements of air pollution levels. Additionally, we show for the first time that the annual amount of NOx pollution emitted by these single point sources is strongly correlated with annual production from individual, colocated copper/cobalt mines and one oil refinery. Studies like this can be used to estimate mine/oil refinery production before companies release their annual reports or (for non‐publicly traded companies) in the absence of such reports. Insufficient emissions from mines claiming high production could indicate production from a different source. Joint analysis of satellite‐derived emissions and mine production reports could be useful in improving the traceability of minerals extracted in conflict areas. Key Points: We quantified annual TROPOspheric Monitoring Instrument (TROPOMI)‐derived NOx emissions from point sources corresponding to copper/cobalt mines, despite high background valuesAnnual emissions from individual point sources are strongly correlated with annual production from colocated single mines, one oil refineryTROPOMI is relevant to monitoring air quality and mining/industrial production in remote regions where these activities are growing rapidly [ABSTRACT FROM AUTHOR]

The Global and Regional Earth System Monitoring Using Satellite and In Situ Data (GEMS) project is combining the manifold expertise in atmospheric composition research and numerical weather prediction of 32 European institutes to build a comprehensive monitoring and forecasting system for greenhouse gases, reactive gases, aerosol, and regional air quality. The project is funded by the European Commission as part of the Global Monitoring of Environment and Security (GMES) framework. GEMS has extended the data assimilation system of the European Centre for Medium-Range Weather Forecasts (ECMWF) to include various tracers for which satellite observations exist. A chemical transport model has been coupled to this system to account for the atmospheric chemistry. The GEMS system provides lateral boundary conditions for a set of 10 regional air quality forecast models and global atmospheric fields for use in surface flux inversions for the greenhouse gases. Observations from both in situ and satellite sources are used as input, and the output products will serve users such as policy makers, environmental agencies, the science community, and providers of end-user services for air quality and health. This article provides an overview of GEMS and uses some recent results to illustrate the current status of the project. It is expected that GEMS will grow into a full operational service for the atmospheric component of GMES in the next decade. Part of this transition will be the merge with the Protocol Monitoring for the GMES Service Element: Atmosphere (PROMOTE) GMES project into the Monitoring of Atmospheric Composition and Climate (MACC) project.