Reactive Nitrogen Partitioning Enhances the Contribution of Canadian Wildfire Plumes to US Ozone Air Quality
Meiyun Lin, Larry W. Horowitz, Lu Hu, Wade Permar
Abstract
Abstract Quantifying the variable impacts of wildfire smoke on ozone air quality is challenging. Here we use airborne measurements from the 2018 Western Wildfire Experiment for Cloud Chemistry, Aerosol Absorption, and Nitrogen (WE‐CAN) to parameterize emissions of reactive nitrogen (NO y ) from wildfires into peroxyacetyl nitrate (PAN; 37%), NO 3 − (27%), and NO (36%) in a global chemistry‐climate model with 13 km spatial resolution over the contiguous US. The NO y partitioning, compared with emitting all NO y as NO, reduces model ozone bias in near‐fire smoke plumes sampled by the aircraft and enhances ozone downwind by 5–10 ppbv when Canadian smoke plumes travel to Washington, Utah, Colorado, and Texas. Using multi‐platform observations, we identify the smoke‐influenced days with daily maximum 8‐hr average (MDA8) ozone of 70–88 ppbv in Kennewick, Salt Lake City, Denver and Dallas. On these days, wildfire smoke enhanced MDA8 ozone by 5–25 ppbv, through ozone produced remotely during plume transport and locally via interactions of smoke plume with urban emissions.