We simulated a scenario representing Northern California for a two-day period. The aerosol mixing state in the region varies spatially as well as temporally due to the spatial distribution of different emission sources, the transport of aerosols and trace gases and the aerosol aging resulting from coagulation and condensation. To quantify the impact of aerosol mixing state on optical properties, a composition-averaging technique was used, which simplifies the highly detailed per-particle composition to a level of detail that lower-detail sectional models are able to represent. The optical properties were calculated using a core-shell Mie code for both the reference simulation, which tracks the full mixing state, and the composition-averaged simulation, which assumes an internal mixture. We then compare absorption and scattering as well as single scattering albedo of the particle-resolved simulation to the composition-averaged simulation.
We present the spatial maps of error in simulated optical properties between the particle-resolved and composition-averaged calculations. We discuss how the differences between the two representations vary as a function of mixing state parameter chi, a metric where values range from 0 – reflecting a fully externally mixed particle population – to 1, reflecting a fully internally mixed particle population.