We have analyzed TROPOMI data over the Copperbelt mining region (Democratic Republic of Congo and Zambia). Despite high background values, we find that annual 2019-2022 means of TROPOMI NO2 show local enhancements consistent with six point sources (mines and cities) where high-emission industrial activities take place. We have quantified annual NO2 emissions for the six sources, identified temporal trends in these emissions, and found strong correlations with mine/refinery production data. CAMS-GLOB-ANT v5 inventory emissions are lower than TROPOMI-derived emissions by 61-96 % and lack the temporal trends observed in TROPOMI and mine/oil refinery production. Lack of TROPOMI SO2 enhancements over the point sources analyzed indicates SO2 capture and transformation into sulfuric acid, a profitable byproduct. These results demonstrate the potential for satellite monitoring of mining/oil refining activity which impacts the air quality of local communities. This is particularly important for Africa, where mining is increasing aggressively.

Modeling atmospheric chemistry across scales with the Multi-Scale Infrastructure for Chemistry and Aerosols (MUSICA) leverages a new regional refinement capability within the NCAR Community Earth System Model (CESM). This framework allows for simultaneous simulation at human-relevant and policy-relevant scales at the same time as hemispheric and global-scales. Here, we present the development of a regional refined grid over the Australian region and assess initial simulations for the 2019/2020 wildfire season. The Australian wildfire events of 2019/2020 saw large local emissions of pollution with wide-scale impacts across the southeast of the continent, where smoke and haze degraded air quality for many days for millions of people. Hemispheric transport of pollution at low and lofted altitudes also occurred, creating an atmospheric signature over New Zealand and South America, and had a direct influence on climate. These multiple-scale impacts from wildfire in the Australian region make it ideal for testing the new capability of multi-scale modeling.

Fire emissions are an important component of global models, which help to understand the influence of sources, transport and chemistry on atmospheric composition. Global fire emission inventories can vary substantially due to the assumptions made in the emission creation process, including the defined vegetation type, fire detection, fuel loading, fraction of vegetation burned and emissions factors. Here, we focus on the uncertainty in emission factors and the resulting impact on modeled composition. Our study uses the Community Atmosphere Model with chemistry (CAM-chem) to model atmospheric composition for 2014, a year chosen for the relatively quiet El Niño Southern Oscillation activity. We focus on carbon monoxide (CO), a trace gas emitted from incomplete combustion and also produced from secondary oxidation of volatile organic compounds (VOCs). Fire is a major source of atmospheric CO and VOCs. Modeled CO from four fire emission inventories (CMIP6/GFED4s, QFED2.5, GFAS1.2 and FINN1.5) are compared after being implemented in CAM-chem. Multiple sensitivity tests are performed based on CO and VOC emission factor uncertainties. We compare model output in the 14 basis regions defined by the Global Fire Emissions Database (GFED) team and evaluate against CO observations from the Measurements of Pollution in the Troposphere (MOPITT) satellite-based instrument. For some regions, emission factor uncertainty spans the results found by using different inventories. Finally, we use modeled ozone (O3) to briefly investigate how emission factor uncertainty influences the atmospheric oxidative environment. Overall, accounting for emission factor uncertainty when modeling atmospheric chemistry can lend a range of uncertainty to simulated results.

Atmospheric carbon monoxide (CO) has been decreasing globally for the last two decades. Recently, positive fire trends in Northern Hemisphere boreal regions may have impacted the decreasing CO. Additionally, time-varying air quality policies will have different impacts on atmospheric composition and related trends. Aerosols are co-emitted with CO from both fires and anthropogenic sources. Consequently, a combined trend analysis of CO and aerosol optical depth (AOD) measurements from space can help elucidate the drivers of regional differences in the CO trend. We use valuable long-term records from two instruments aboard the Terra satellite. Measurements of Pollution in the Troposphere (MOPITT) CO and AOD from the Moderate Resolution Imaging Spectroradiometer (MODIS) instrument are examined hemispherically and in sub-regions to determine trends between 2002 and 2018. The records are further split into two sub-periods in order to examine temporal stability in the trend values. We also assess the CO trends in monthly percentile values to use seasonal information when interpreting trend contributions. Our focus is on four major population centers: Southeast USA, Europe, Northeast China and North India, as well as biomass burning regions in both hemispheres. Our results show that globally, CO declines faster in the first half of the record compared to the second half. Both atmospheric species are important when interpreting trends in the smaller regions. Northern Hemisphere boreal fire regions show a regime-shift in their seasonality for both CO and AOD, which may counteract the downward trend in CO. Anthropogenic regions with minimal air quality management such as North India become more globally relevant as the global CO trend weakens. We also find clear evidence of the atmospheric impact of policy choices. Overall, we observe that local changes in biomass burning and air quality can counteract the global downward trend in CO.

Wildfire emissions can vary substantially between different inventories due to the assumptions made in the emission creation process, including the defined vegetation type, fire detection, fuel loading, fraction of vegetation burned and emissions factors. Here, we focus on the uncertainty in emission factors and the resulting impact on modeled composition. We use the Community Atmosphere Model with chemistry (CAM-chem) to simulate 2014 atmospheric composition and focus on carbon monoxide (CO), a trace gas emitted from incomplete combustion and also produced from secondary oxidation of volatile organic compounds (VOCs). Fire is a major source of atmospheric CO and VOCs. Multiple simulations are compared, from an ensemble using four fire emission inventories (CMIP6/GFED4s, QFED2.5, GFAS1.2 and FINN1.5) and a range of sensitivity tests based on CO and VOC emission factor uncertainties. We compare model output and evaluate against CO observations from the Measurements of Pollution in the Troposphere (MOPITT) satellite-based instrument. For some regions, emission factor uncertainty spans the results found by using different inventories. Finally, we use modeled ozone (O3) to investigate how emission factor uncertainty influences the atmospheric oxidative environment. Overall, accounting for emission factor uncertainty lends a range of uncertainty to simulated results.