Abstract. Fires emit a substantial amount of non-methane organic gases (NMOGs), theatmospheric oxidation of which can contribute to ozone and secondaryparticulate matter formation. However, the abundance and reactivity of thesefire NMOGs are uncertain and historically not well constrained. In thiswork, we expand the representation of fire NMOGs in a global chemicaltransport model, GEOS-Chem. We update emission factors to Andreae (2019) andthe chemical mechanism to include recent aromatic and ethene and ethyne modelimprovements(Bateset al., 2021; Kwon et al., 2021). We expand the representation of NMOGs byadding lumped furans to the model (including their fire emission andoxidation chemistry) and by adding fire emissions of nine species alreadyincluded in the model, prioritized for their reactivity using data from the Fire Influence on Regional to Global Environments (FIREX) laboratory studies. Based on quantified emissions factors, we estimatethat our improved representation captures 72 % of emitted, identified NMOGcarbon mass and 49 % of OH reactivity from savanna and temperate forestfires, a substantial increase from the standard model (49 % of mass,28 % of OH reactivity). We evaluate fire NMOGs in our model withobservations from the Amazon Tall Tower Observatory (ATTO) in Brazil, Fire Influence on Regional to Global Environments and Air Quality (FIREX-AQ) and DC3 in the US, and Arctic Research of the Composition of theTroposphere from Aircraft and Satellites (ARCTAS) in boreal Canada. We show that NMOGs,including furan, are well simulated in the eastern US with someunderestimates in the western US and that adding fire emissions improves ourability to simulate ethene in boreal Canada. We estimate that fires provide15 % of annual mean simulated surface OH reactivity globally, as well as morethan 75 % over fire source regions. Over continental regions about half ofthis simulated fire reactivity comes from NMOG species. We find that furansand ethene are important globally for reactivity, while phenol is moreimportant at a local level in the boreal regions. This is the first globalestimate of the impact of fire on atmospheric reactivity.
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Effects of Fire Diurnal Variation and Plume Rise on U.S. Air Quality During FIREX‐AQ and WE‐CAN Based on the Multi‐Scale Infrastructure for Chemistry and Aerosols (MUSICAv0)
We analyze the effects of the diurnal cycle of fire emissions (DCFE) and plume rise on U.S. air quality using the MUSICAv0 (Multi‐Scale Infrastructure for Chemistry and Aerosols Version 0) model during the FIREX‐AQ (Fire Influence on Regional to Global Environments and Air Quality) and WE‐CAN (Western wildfire Experiment for Cloud chemistry, Aerosol absorption and Nitrogen) field campaigns. To include DCFE in the model, we employ two approaches: a DCFE climatology and DCFE derived from a satellite fire radiative power product. We also implemented two sets of plume‐rise climatologies, and two plume‐rise parameterizations. We evaluate the model performance with airborne measurements, U.S. EPA Air Quality System surface measurements, and satellite products. Overall, including plume rise improves model agreement with observations such as aircraft observations of CO and NOxfor FIREX‐AQ and WE‐CAN. Applying DCFE also improves model performance, such as for surface PM2.5in fire‐impacted regions. The impact of plume rise is larger than the impact of DCFE. Plume rise can greatly enhance modeled long‐range transport of fire‐emitted pollutants. The simulations with plume‐rise parameterizations generally perform better than the simulations with plume‐rise climatologies during FIREX‐AQ, but not for WE‐CAN. The 2019 Williams Flats Fire case study demonstrates that DCFE and plume rise change fire impacts because fire emissions are subject to different meteorology and chemistry when emitted at different times of a day and altitudes. Moreover, DCFE and plume rise also impact local‐to‐regional meteorology and chemical reaction rates. DCFE and plume rise will be included in future MUSICA versions.
more » « less- PAR ID:
- 10372051
- Author(s) / Creator(s):
- ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; more »
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Journal of Geophysical Research: Atmospheres
- Volume:
- 127
- Issue:
- 16
- ISSN:
- 2169-897X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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