Measurements To Determine The Mixing State Of Black Carbon Emitted From The 2017-2018 California Wildfires And Urban Los Angeles

The effects of atmospheric black carbon (BC) on climate and public health have been well established, but large uncertainties remain regarding the extent of the impacts of BC at different temporal and spatial scales. These uncertainties are largely due to the heterogeneous nature of BC in terms of its spatiotemporal distribution, mixing state, and coating composition. Here, we seek to further understand the size and mixing state of BC emitted from various sources and aged over different timescales using field measurements in the Los Angeles region. We measured refractory black carbon (rBC) with a single-particle soot photometer (SP2) on Catalina Island, California (similar to 70 km southwest of downtown Los Angeles) during three different time periods. During the first campaign (September 2017), westerly winds were dominant and measured air masses were representative of wellaged background over the Pacific Ocean. In the second and third campaigns (December 2017 and November 2018, respectively), atypical Santa Ana wind conditions allowed us to measure biomass burning rBC (BCbb) from air masses dominated by large biomass burning events in California and fossil fuel rBC (BCff) from the Los Angeles Basin. We observed that the emissions source type heavily influenced both the size distribution of the rBC cores and the rBC mixing state. BCbb had thicker coatings and larger core diameters than BBff. We observed a mean coating thickness (CTBc) of similar to 40-70 nm and a count mean diameter (CMD) of similar to 120 nm for BCbb. For BCff, we observed a CTBc of similar to 5-15 nm and a CMD of similar to 100 nm. Our observations also provided evidence that aging led to an increased CTBc for both BCbb and BCff . Aging timescales < similar to 1 d were insufficient to thickly coat freshly emitted BCff. However, CTBc for aged B-ff within aged background plumes was similar to 35 nm thicker than CTBc for fresh BCff. Likewise, we found that CTBc for aged BCbb was similar to 18 nm thicker than CTBc for fresh BCbb. The results presented in this study highlight the wide variability in the BC mixing state and provide additional evidence that the emissions source type and aging influence rBC microphysical properties.