Mobile sampling studies have revealed
enhanced levels of secondary
organic aerosol (SOA) in source-rich urban environments. While these
enhancements can be from rapidly reacting vehicular emissions, it
was recently hypothesized that nontraditional emissions (volatile
chemical products and upstream emissions) are emerging as important
sources of urban SOA. We tested this hypothesis by using gas and aerosol
mass spectrometry coupled with an oxidation flow reactor (OFR) to
characterize pollution levels and SOA potentials in environments influenced
by traditional emissions (vehicular, biogenic), and nontraditional
emissions (e.g., paint fumes). We used two SOA models to assess contributions
of vehicular and biogenic emissions to our observed SOA. The largest
gap between observed and modeled SOA potential occurs in the morning-time
urban street canyon environment, for which our model can only explain
half of our observation. Contributions from VCP emissions (e.g., personal
care products) are highest in this environment, suggesting that VCPs
are an important missing source of precursors that would close the
gap between modeled and observed SOA potential. Targeted OFR oxidation
of nontraditional emissions shows that these emissions have SOA potentials
that are similar, if not larger, compared to vehicular emissions.
Laboratory experiments reveal large differences in SOA potentials
of VCPs, implying the need for further characterization of these nontraditional
emissions.