Back to Search Start Over

Airborne Observations Constrain Heterogeneous Nitrogen and Halogen Chemistry on Tropospheric and Stratospheric Biomass Burning Aerosol

Authors :
Decker, Zachary C. J.
Novak, Gordon A.
Aikin, Kenneth
Veres, Patrick R.
Neuman, J. Andrew
Bourgeois, Ilann
Bui, T. Paul
Campuzano‐Jost, Pedro
Coggon, Matthew M.
Day, Douglas A.
DiGangi, Joshua P.
Diskin, Glenn S.
Dollner, Maximilian
Franchin, Alessandro
Fredrickson, Carley D.
Froyd, Karl D.
Gkatzelis, Georgios I.
Guo, Hongyu
Hall, Samuel R.
Halliday, Hannah
Hayden, Katherine
Holmes, Christopher D.
Jimenez, Jose L.
Kupc, Agnieszka
Lindaas, Jakob
Middlebrook, Ann M.
Moore, Richard H.
Nault, Benjamin A.
Nowak, John B.
Pagonis, Demetrios
Palm, Brett B.
Peischl, Jeff
Piel, Felix M.
Rickly, Pamela S.
Robinson, Michael A.
Rollins, Andrew W.
Ryerson, Thomas B.
Schill, Gregory P.
Sekimoto, Kanako
Thompson, Chelsea R.
Thornhill, Kenneth L.
Thornton, Joel A.
Ullmann, Kirk
Warneke, Carsten
Washenfelder, Rebecca A.
Weinzierl, Bernadett
Wiggins, Elizabeth B.
Williamson, Christina J.
Winstead, Edward L.
Wisthaler, Armin
Womack, Caroline C.
Brown, Steven S.
Source :
Geophysical Research Letters; February 2024, Vol. 51 Issue: 4
Publication Year :
2024

Abstract

Heterogeneous chemical cycles of pyrogenic nitrogen and halides influence tropospheric ozone and affect the stratosphere during extreme Pyrocumulonimbus (PyroCB) events. We report field‐derived N2O5uptake coefficients, γ(N2O5), and ClNO2yields, φ(ClNO2), from two aircraft campaigns observing fresh smoke in the lower and mid troposphere and processed/aged smoke in the upper troposphere and lower stratosphere (UTLS). Derived φ(ClNO2) varied across the full 0–1 range but was typically <0.5 and smallest in a PyroCB (<0.05). Derived γ(N2O5) was low in agricultural smoke (0.2–3.6 × 10−3), extremely low in mid‐tropospheric wildfire smoke (0.1 × 10−3), but larger in PyroCB processed smoke (0.7–5.0 × 10−3). Aged biomass burning aerosol in the UTLS had a higher γ(N2O5) of 17 × 10−3that increased with sulfate and liquid water, but that was 1–2 orders of magnitude lower than values for aqueous sulfuric aerosol used in stratospheric models. The injection of reactive material into Earth's atmosphere from fires affects atmospheric composition at regional and hemispheric scales. Reported stratospheric ozone depletion during extreme events, such as the 2020 Australian wildfires, illustrates one example of fire impacts and the role of heterogeneous (gas‐particle) processes. We report field quantification of rates and product yields from airborne observations of smoke. Extremely slow heterogeneous reaction rates on young smoke increase with transport and aging, but upper atmospheric values are still a factor of 10 slower than parameterizations used in stratospheric models. Heterogeneous production of ClNO2, a major lower atmospheric chlorine activation pathway, may be active on biomass burning aerosol in the upper atmosphere. ClNO2formation is active on biomass burning (BB) particles but decreases with transport to the upper troposphere and lower stratosphere (UTLS)N2O5uptake coefficients are low on young BB smoke and increase with transport through a PyroCB and UTLS agingN2O5uptake coefficients on aged BB particles in the UTLS are significantly lower than those used in model parameterizations ClNO2formation is active on biomass burning (BB) particles but decreases with transport to the upper troposphere and lower stratosphere (UTLS) N2O5uptake coefficients are low on young BB smoke and increase with transport through a PyroCB and UTLS aging N2O5uptake coefficients on aged BB particles in the UTLS are significantly lower than those used in model parameterizations

Details

Language :
English
ISSN :
00948276
Volume :
51
Issue :
4
Database :
Supplemental Index
Journal :
Geophysical Research Letters
Publication Type :
Periodical
Accession number :
ejs65576062
Full Text :
https://doi.org/10.1029/2023GL107273