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- Title
Emissions of Reactive Nitrogen From Western U.S. Wildfires During Summer 2018.
- Authors
Lindaas, Jakob; Pollack, Ilana B.; Garofalo, Lauren A.; Pothier, Matson A.; Farmer, Delphine K.; Kreidenweis, Sonia M.; Campos, Teresa L.; Flocke, Frank; Weinheimer, Andrew J.; Montzka, Denise D.; Tyndall, Geoffrey S.; Palm, Brett B.; Peng, Qiaoyun; Thornton, Joel A.; Permar, Wade; Wielgasz, Catherine; Hu, Lu; Ottmar, Roger D.; Restaino, Joseph C.; Hudak, Andrew T.
- Abstract
Reactive nitrogen (Nr) within smoke plumes plays important roles in the production of ozone, the formation of secondary aerosols, and deposition of fixed N to ecosystems. The Western Wildfire Experiment for Cloud Chemistry, Aerosol Absorption, and Nitrogen (WE‐CAN) field campaign sampled smoke from 23 wildfires throughout the western U.S. during summer 2018 using the NSF/NCAR C‐130 research aircraft. We empirically estimate Nr normalized excess mixing ratios and emission factors from fires sampled within 80 min of estimated emission and explore variability in the dominant forms of Nr between these fires. We find that reduced N compounds comprise a majority (39%–80%; median = 66%) of total measured reactive nitrogen (ΣNr) emissions. The smoke plumes sampled during WE‐CAN feature rapid chemical transformations after emission. As a result, within minutes after emission total measured oxidized nitrogen (ΣNOy) and measured total ΣNHx (NH3 + pNH4) are more robustly correlated with modified combustion efficiency (MCE) than NOx and NH3 by themselves. The ratio of ΣNHx/ΣNOy displays a negative relationship with MCE, consistent with previous studies. A positive relationship with total measured ΣNr suggests that both burn conditions and fuel N content/volatilization differences contribute to the observed variability in the distribution of reduced and oxidized Nr. Additionally, we compare our in situ field estimates of Nr EFs to previous lab and field studies. For similar fuel types, we find ΣNHx EFs are of the same magnitude or larger than lab‐based NH3 EF estimates, and ΣNOy EFs are smaller than lab NOx EFs. Plain Language Summary: Smoke from large wildfires in the western U.S. degrades air quality across the whole U.S. Smoke contains a mixture of many different gases and particles, including carbon compounds like carbon dioxide and carbon monoxide, as well as nitrogen compounds such as ammonia and nitrogen oxides. Gases containing nitrogen are important for the production of ozone and the formation of more or larger particles as the smoke moves downwind. During the summer of 2018, we used the National Science Foundation/National Center for Atmospheric Research C130 research aircraft to fly through smoke across the western U.S. and measure many of the most abundant nitrogen compounds. We find that the smoke plumes we sampled emitted more nitrogen in a reduced form than in an oxidized form, and chemical reactions change the form and phase of nitrogen very quickly in the smoke. We compare our field measurements with laboratory measurements with the goal of using them together to improve our forecasts of how and where wildfire smoke will impact air quality. Key Points: Normalized excess mixing ratios of nitrogen species are reported for western U.S. wildfires; median of 66% of emissions are in reduced formWithin minutes after emission, rapid chemistry changes the distribution (species/amount/phase) of reactive nitrogen in fresh smoke plumesFor similar fuel types, NHx emissions factors are similar to or higher than lab‐based estimates; NOy emission factors are smaller
- Subjects
UNITED States; WILDFIRES &; the environment; NITROGEN &; the environment; WILDFIRES; EMISSIONS (Air pollution); SMOKE plumes; OZONE
- Publication
Journal of Geophysical Research. Atmospheres, 2021, Vol 126, Issue 2, p1
- ISSN
2169-897X
- Publication type
Article
- DOI
10.1029/2020JD032657