Highly Time-Resolved Apportionment of Carbonaceous Aerosols from Wildfire Using the TC–BC Method: Camp Fire 2018 Case Study

Abstract

The Camp Fire was one of California’s deadliest and most destructive wildfires, and its widespread smoke threatened human health over a large area in Northern California in November 2018. To analyze the Camp Fire influence on air quality on a 200 km distant site in Berkeley, highly time-resolved total carbon (TC), black carbon (BC), and organic carbon (OC) were measured using the Carbonaceous Aerosol Speciation System (CASS, Aerosol Magee Scientific), comprising two instruments, a Total Carbon Analyzer TCA08 in tandem with an Aethalometer AE33. During the period when the air quality was affected by wildfire smoke, the BC concentrations increased four times above the typical air pollution level presented in Berkeley before and after the event, and the OC increased approximately ten times. High-time-resolution measurements allow us to study the aging of OC and investigate how the characteristics of carbonaceous aerosols evolve over the course of the fire event. A higher fraction of secondary carbonaceous aerosols was observed in the later phase of the fire. At the same time, the amount of light-absorbing organic aerosol (brown carbon) declined with time.