This study examines the nature of water-soluble organic aerosol measured in Pasadena, CA, under typical conditions and under the influence of a large wildfire (the 2009 Station Fire). During non-fire periods, water-soluble organic carbon (WSOC) variability was driven by photochemical production processes and sea breeze transport, resulting in an average diurnal cycle with a maximum at 15:00 local time (up to 4.9 μg C m^(−3)). During the Station Fire, primary production was a key formation mechanism for WSOC. High concentrations of WSOC (up to 41 μg C m^(−3)) in smoke plumes advected to the site in the morning hours were tightly correlated with nitrate and chloride, numerous aerosol mass spectrometer (AMS) organic mass spectral markers, and total non-refractory organic mass. Processed residual smoke was transported to the measurement site by the sea breeze later in the day, leading to higher afternoon WSOC levels than on non-fire days. Parameters representing higher degrees of oxidation of organics, including the ratios of the organic metrics m/z 44:m/z 57 and m/z 44:m/z 43, were elevated in those air masses. Intercomparisons of relative amounts of WSOC, organics, m/z 44, and m/z 43 show that the fraction of WSOC comprising acid-oxygenates increased as a function of photochemical aging owing to the conversion of aliphatic and non-acid oxygenated organics to more acid-like organics. 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. The seasonal incidence of wildfires in the Los Angeles Basin greatly enhances the importance of water-soluble organics, which has implications for the radiative and hygroscopic properties of the regional aerosol
