Quantifies contributions of semivolatile organic aerosols in coastal urban environments, suggesting significant impact on aerosol properties.
Organic components often contribute 50% or more of the submicron aerosol mass in coastal urban environments, but their partitioning between the gas and particle phases is controlled by a complex mixture of unidentified organic compounds that are poorly constrained by observations. This study compares daily filter organic functional groups (OFG) with online organic mass fragments from La Jolla, California, as part of the Eastern Pacific Cloud Aerosol Precipitation Experiment (EPCAPE), quantifying the contributions of four types of nonvolatile (NV) organic emission sources to the submicron composition. Daily filters retained only 0.79–0.98 µg/m3 NV submicron organic mass concentration, even though 1.8–1.9 µg/m3 non-refractory (NR) submicron organic mass concentration was measured online. The 62–64% of measured NR submicron organic mass concentration that exceeded what remained on the filters after 23-h sampling is interpreted as semi-volatile, consistent with the moderate correlation of the NR OM–NV OM difference to NR ammonium, NR nitrate, and biomass burning-related NV and NR organic factors. The association between semi-volatile organic components and ammonium nitrate likely results from both co-emission and co-evaporation. Size-resolved filter analysis showed that NV organic mass concentration accounts for 68% of NR organic mass concentration for 0.5–1 µm dry diameter, but account for 9.0% for 0.18–0.5 µm dry diameter, showing the differences in volatility between particle modes. Importantly, the volatility of organic components was size-dependent and associated with ammonium nitrate and biomass burning, providing guidance for constraining atmospheric aerosol properties in global models.
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Pelayo et al. (2026) studied this question.
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