Atmospheric aerosols play an important role in the global climate system via modification of the radiation budget directly, by scattering and absorption, as well as indirectly, by modifying cloud properties (Boucher et al., 2013). Near-surface observations over the USA in the latter part of the twentieth century and early twenty-first century indicated PM 2.5 mass was typically dominated by sulphate ( 2 4 SO ) and nitrate ( 3 NO ) in combination with ammonium ( 4NH ), followed by organic carbon (OC) and then black (elemental) carbon (BC) Shah et al., 2018). An analysis of data at rural and urban stations over the eastern USA during 2005-2008 found ammonium sulphate contributed an average of 40% of the annual mean and up to 60% of PM 2.5 mass in the summer. Ammonium nitrate comprised a much lower fraction of total PM 2.5 but was considerably more prevalent in urban than rural locations, in winter than in summer and in the MidWest (MW) than other parts of the eastern USA. Organics comprised 20%-30% of mean near-surface PM 2.5 mass, were highest in the southeastern USA, and demonstrate modest seasonality but a summer maximum. Elemental carbon was highest in urban areas but typically comprises only a few percent of total near-surface PM 2.5 mass . Model-based analyses of summertime aerosol optical depth (AOD) over the eastern USA indicate sulphate also dominates summertime total AOD and direct aerosol radiative forcing followed by OC, BC, and dust with nitrate playing only a minor role (Paulot et al., 2018).According to annual U.S. National Emissions Inventories (NEIs), emission control measures implemented under the Clean Air Act have preferentially reduced emissions of sulfur dioxide (SO 2 ) relative to emissions