Decreasing Aerosol Water Is Consistent with OC Trends in the Southeast U.S

• Published in: Environmental science & technology Vol. 49; no. 13; pp. 7843 - 7850
• Main Authors: Nguyen, Thien Khoi V, Capps, Shannon L, Carlton, Annmarie G
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 07.07.2015
• Subjects: Aerosols; Aerosols - chemistry; Atmospheric aerosols; Atmospheric chemistry; Light; Models, Theoretical; Organic Chemicals - chemistry; Particulate Matter - analysis; Regression Analysis; Scattering; Southeastern United States; Thermodynamics; Trends; Water; Water - chemistry; United States > US
• ISSN: 0013-936X; 1520-5851
• DOI: 10.1021/acs.est.5b00828

Water is a ubiquitous and abundant component of atmospheric aerosols. It influences light scattering, the hydrological cycle, atmospheric chemistry, and secondary particulate matter (PM) formation. Despite the critical importance of aerosol liquid water, mass concentrations are not well-known. Using speciated ion and meteorological data from the Southeastern Aerosol Research and Characterization network, we employ the thermodynamic model ISORROPIAv2.1 to estimate water mass concentrations and evaluate trends from 2001 to 2012 in urban and rural locations. The purpose of this study is to better understand the historical trends of aerosol liquid water in the southeast U.S. in the context of improved air quality and recently noted reductions in particulate organic carbon (OC). Aerosol water mass concentrations decrease by ∼79% from 2001 to 2012 in the region. Decreases are more prominent in rural than in urban areas. Fractional contribution of water to PM also decreases during the same time period, and this is consistent with recently noted improvements in visibility. These findings agree with the hypotheses that aerosol liquid water facilitates formation of biogenic secondary organic aerosol (SOA) and that biogenically derived SOA is modulated in the presence of anthropogenic perturbations.