Atmos. Chem. Phys. Discuss., 11, 12849-12887, 2011
www.atmos-chem-phys-discuss.net/11/12849/2011/
doi:10.5194/acpd-11-12849-2011
© Author(s) 2011. This work is distributed
under the Creative Commons Attribution 3.0 License.
Review Status
This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Impact of a large wildfire on water-soluble organic aerosol in a major urban area: the 2009 Station Fire in Los Angeles County
A. Wonaschütz1, S. P. Hersey2, A. Sorooshian1,3, J. S. Craven2, A. R. Metcalf2, R. C. Flagan2, and J. H. Seinfeld2
1Department of Atmospheric Sciences, University of Arizona, P.O. Box 210081, Tucson, AZ 85721, USA
2Departments of Environmental Science and Engineering and Chemical Engineering, California Institute of Technology, 1200 E. California Blvd., Pasadena, CA 91125, USA
3Department of Chemical and Environmental Engineering, University of Arizona, P.O. Box 210011, Tucson, AZ 85721, USA

Abstract. Water-soluble organic carbon is a major component of aerosol particles globally. This study examines a field dataset of water-soluble organic aerosol in the Los Angeles Basin, a classic urban setting, under typical conditions and under the influence of a large wildfire (the 2009 Station Fire). The measurements took place between July and September in Pasadena as part of the 2009 Pasadena Aerosol Characterization Observatory (PACO) field campaign. Large differences in the nature of water-soluble organic carbon (WSOC) were observed between periods with and without the influence of the fire. During non-fire periods, WSOC variability was driven most likely by a combination of photochemical production processes and subsequent sea breeze transport, resulting in an average diurnal cycle with a maximum at 15:00 LT (up to 4.9 μg C m−3). During the Station Fire, smoke plumes advected to the site in the morning hours were characterized by high concentrations of WSOC (up to 41 μg C m−3) in tight correlation with nitrate and chloride, and with Aerodyne Aerosol Mass Spectrometer (AMS) organic metrics such as the biomass burning tracer m/z 60, and total non-refractory organic mass. These concentrations and correlations and the proximity of the measurement site to the fire suggest that primary production was a key formation mechanism for WSOC. During the afternoons, the sea breeze transported urban pollution and processed residual smoke back to the measurement site, leading to higher afternoon WSOC levels than on non-fire days. Parameters representing higher degrees of oxidation of organics, including the ratios m/z 44 : m/z 57 and m/z 44 : m/z 43, were increased in those air masses. Intercomparisons of relative amounts of WSOC, AMS organic, m/z 44, and m/z 43 are used to examine how the relative abundance of different classes of WSOC species changed as a result of photochemical aging. The fraction of WSOC comprised of acid-oxygenates increased as a of photochemical aging owing to the conversion of aliphatic and non-acid oxygenated organics to more acid-like organics. Assuming a factor of 1.8 to convert WSOC concentrations to organic mass-equivalent concentrations, the contribution of water-soluble organic species to the organic mass budget (10th–90th percentile values) ranged between 27–72% and 27–68% during fire and non-fire periods, respectively. Therefore, WSOC is a significant contributor to the organic aerosol budget in this urban area. The influence of fires in this basin greatly enhances the importance of this class of organics, which has implications for the radiative and hygroscopic properties of the regional aerosol.

Citation: Wonaschütz, A., Hersey, S. P., Sorooshian, A., Craven, J. S., Metcalf, A. R., Flagan, R. C., and Seinfeld, J. H.: Impact of a large wildfire on water-soluble organic aerosol in a major urban area: the 2009 Station Fire in Los Angeles County, Atmos. Chem. Phys. Discuss., 11, 12849-12887, doi:10.5194/acpd-11-12849-2011, 2011.
 
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