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Abstract The Western Wildfire Experiment for Cloud Chemistry, Aerosol Absorption, and Nitrogen (WE‐CAN) deployed the NSF/NCAR C‐130 aircraft in summer 2018 across the western U.S. to sample wildfire smoke during its first days of atmospheric evolution. We present a summary of a subset of reactive oxidized nitrogen species (NOy) in plumes sampled in a pseudo‐Lagrangian fashion. Emissions of nitrogen oxides (NOx = NO + NO2) and nitrous acid (HONO) are rapidly converted to more oxidized forms. Within 4 h, ∼86% of the ΣNOyis in the form of peroxy acyl nitrates (PANs) (∼37%), particulate nitrate (pNO3) (∼27%), and gas‐phase organic nitrates (Org N(g)) (∼23%). The averagee‐folding time and distance for NOxare ∼90 min and ∼40 km, respectively. Nearly no enhancements in nitric acid (HNO3) were observed in plumes sampled in a pseudo‐Lagrangian fashion, implying HNO3‐limited ammonium nitrate (NH4NO3) formation, with one notable exception that we highlight as a case study. We also summarize the observed partitioning of NOyin all the smoke samples intercepted during WE‐CAN. In smoke samples intercepted above 3 km above sea level (ASL), the contributions of PANs andpNO3to ΣNOyincrease with altitude. WE‐CAN also sampled smoke from multiple fires mixed with anthropogenic emissions over the California Central Valley. We distinguish samples where anthropogenic NOxemissions appear to lead to an increase in NOxabundances by a factor of four and contribute to additional PAN formation.
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Unexpected Repartitioning of Stratospheric Inorganic Chlorine After the 2020 Australian Wildfires
Abstract The inorganic chlorine (Cly) and odd nitrogen (NOy) chemical families influence stratospheric O3. In January 2020 Australian wildfires injected record‐breaking amounts of smoke into the southern stratosphere. Within 1–2 months ground‐based and satellite observations showed Clyand NOywere repartitioned. By May, lower stratospheric HCl columns declined by ∼30% and ClONO2columns increased by 40%–50%. The Clyperturbations began and ended near the equinoxes, increased poleward, and peaked at the winter solstice. NO2decreased from February to April, consistent with sulfate aerosol reactions, but returned to typical values by June ‐ months before the Clyrecovery. Transport tracers show that dynamics not chemistry explains most of the observed O3decrease after April, with no significant transport earlier. Simulations assuming wildfire smoke behaves identically to sulfate aerosols couldn't reproduce observed Clychanges, suggesting they have different composition and chemistry. This undermines our ability to predict ozone in a changing climate.
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- PAR ID:
- 10370611
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Geophysical Research Letters
- Volume:
- 49
- Issue:
- 14
- ISSN:
- 0094-8276
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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