Ozone chemistry in western U.S. wildfire plumes.

Abstract

Wildfires are a substantial but poorly quantified source of tropospheric ozone (O₃). Here, to investigate the highly variable O₃ chemistry in wildfire plumes, we exploit the in situ chemical characterization of western wildfires during the FIREX-AQ flight campaign and show that O₃ production can be predicted as a function of experimentally constrained OH exposure, volatile organic compound (VOC) reactivity, and the fate of peroxy radicals. The O₃ chemistry exhibits rapid transition in chemical regimes. Within a few daylight hours, the O₃ formation substantially slows and is largely limited by the abundance of nitrogen oxides (NO<i>_x</i>). This finding supports previous observations that O₃ formation is enhanced when VOC-rich wildfire smoke mixes into NO<i>_x</i>-rich urban plumes, thereby deteriorating urban air quality. Last, we relate O₃ chemistry to the underlying fire characteristics, enabling a more accurate representation of wildfire chemistry in atmospheric models that are used to study air quality and predict climate.