Long-term observational constraints of organic aerosol dependence on inorganic species in the southeast US Atmospheric Chemistry and Physics

Organic aerosol (OA), with a large biogenic fraction in the summertime southeast US, adversely impacts air quality and human health. Stringent air quality controls have recently reduced anthropogenic pollutants including sulfate, whose impact on OA remains unclear. Three filter measurement networks provide long-term constraints on the sensitivity of OA to changes in inorganic species, including sulfate and ammonia. The 2000–2013 summertime OA decreases by 1.7 % yr−1–1.9 % yr−1 with little month-to-month variability, while sulfate declines rapidly with significant monthly difference in the early 2000s. In contrast, modeled OA from a chemical-transport model (GEOS-Chem) decreases by 4.9 % yr−1 with much larger monthly variability, largely due to the predominant role of acid-catalyzed reactive uptake of epoxydiols (IEPOX) onto sulfate. The overestimated modeled OA dependence on sulfate can be improved by implementing a coating effect and assuming constant aerosol acidity, suggesting the needs to revisit IEPOX reactive uptake in current models. Our work highlights the importance of secondary OA formation pathways that are weakly dependent on inorganic aerosol in a region that is heavily influenced by both biogenic and anthropogenic emissions. Grant no. NA18OAR4310112 Grant no. NA18OAR4310114