Articles | Volume 22, issue 18
https://doi.org/10.5194/acp-22-12093-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/acp-22-12093-2022
© Author(s) 2022. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Research article
| 
19 Sep 2022
Research article |
| 19 Sep 2022
| 19 Sep 2022
An improved representation of fire non-methane organic gases (NMOGs) in models: emissions to reactivity
Civil and Environmental Engineering Department, Massachusetts
Institute of Technology, Cambridge, MA 02139, USA
Civil and Environmental Engineering Department, Massachusetts
Institute of Technology, Cambridge, MA 02139, USA
Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of
Technology, Cambridge, MA 02139, USA
Jesse H. Kroll
Civil and Environmental Engineering Department, Massachusetts
Institute of Technology, Cambridge, MA 02139, USA
Eric C. Apel
Atmospheric Chemistry Observations & Modeling Laboratory, National
Center for Atmospheric Research, Boulder, CO 80301, USA
Donald Blake
Chemistry Department, University of California Irvine, Irvine, CA 92697, USA
Matthew Coggon
Chemical Sciences Laboratory, National Oceanic and Atmospheric Administration, Boulder, CO 80305, USA
Achim Edtbauer
Atmospheric Chemistry Department, Max Planck Institute for Chemistry,
55128 Mainz, Germany
Georgios Gkatzelis
Chemical Sciences Laboratory, National Oceanic and Atmospheric Administration, Boulder, CO 80305, USA
Cooperative Institute for Research in Environmental Sciences,
University of Colorado Boulder, Boulder, CO, USA
now at: Institute of Energy and Climate Research, IEK-8:
Troposphere, Forschungszentrum Jülich GmbH, Jülich, Germany
Rebecca S. Hornbrook
Atmospheric Chemistry Observations & Modeling Laboratory, National
Center for Atmospheric Research, Boulder, CO 80301, USA
Jeff Peischl
Chemical Sciences Laboratory, National Oceanic and Atmospheric Administration, Boulder, CO 80305, USA
Cooperative Institute for Research in Environmental Sciences,
University of Colorado Boulder, Boulder, CO, USA
Eva Y. Pfannerstill
Atmospheric Chemistry Department, Max Planck Institute for Chemistry,
55128 Mainz, Germany
now at: Department of Environmental Science, Policy, and
Management, University of California, Berkeley, CA 94720, USA
Felix Piel
IONICON Analytik GmbH, Innsbruck, Austria
Department of Chemistry, University of Oslo, Oslo, Norway
Nina G. Reijrink
Atmospheric Chemistry Department, Max Planck Institute for Chemistry,
55128 Mainz, Germany
IMT Nord Europe, Institut Mines-Télécom, Univ. Lille, Center
for Energy and Environment, 59000 Lille, France
Akima Ringsdorf
Atmospheric Chemistry Department, Max Planck Institute for Chemistry,
55128 Mainz, Germany
Carsten Warneke
Chemical Sciences Laboratory, National Oceanic and Atmospheric Administration, Boulder, CO 80305, USA
Jonathan Williams
Atmospheric Chemistry Department, Max Planck Institute for Chemistry,
55128 Mainz, Germany
Armin Wisthaler
Department of Chemistry, University of Oslo, Oslo, Norway
Institute for Ion Physics and Applied Physics, University of
Innsbruck, Innsbruck, Austria
Division of Geological and Planetary Sciences, California Institute
of Technology, Pasadena, CA 91125, USA
now at: Cooperative Institute for Research in Environmental Sciences,
University of Colorado Boulder, Boulder, CO, USA
now at: Chemical Sciences Laboratory, National Oceanic and Atmospheric Administration, Boulder, CO 80305, USA
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Cited
8 citations as recorded by crossref.
- Evolution of organic carbon in the laboratory oxidation of biomass-burning emissions K. Nihill et al. 10.5194/acp-23-7887-2023
- Constraining emissions of volatile organic compounds from western US wildfires with WE-CAN and FIREX-AQ airborne observations L. Jin et al. 10.5194/acp-23-5969-2023
- Emission Factors for Crop Residue and Prescribed Fires in the Eastern US During FIREX‐AQ K. Travis et al. 10.1029/2023JD039309
- Space-Based Observations of Ozone Precursors within California Wildfire Plumes and the Impacts on Ozone-NOx-VOC Chemistry X. Jin et al. 10.1021/acs.est.3c04411
- NEIVAv1.0: Next-generation Emissions InVentory expansion of Akagi et al. (2011) version 1.0 S. Binte Shahid et al. 10.5194/gmd-17-7679-2024
- Observational evidence reveals the significance of nocturnal chemistry in seasonal secondary organic aerosol formation L. Liu et al. 10.1038/s41612-024-00747-6
- Emissions and Atmospheric Chemistry of Furanoids from Biomass Burning: Insights from Laboratory to Atmospheric Observations M. Romanias et al. 10.1021/acsearthspacechem.3c00226
- Evolution of Reactive Organic Compounds and Their Potential Health Risk in Wildfire Smoke H. Pye et al. 10.1021/acs.est.4c06187
8 citations as recorded by crossref.
- Evolution of organic carbon in the laboratory oxidation of biomass-burning emissions K. Nihill et al. 10.5194/acp-23-7887-2023
- Constraining emissions of volatile organic compounds from western US wildfires with WE-CAN and FIREX-AQ airborne observations L. Jin et al. 10.5194/acp-23-5969-2023
- Emission Factors for Crop Residue and Prescribed Fires in the Eastern US During FIREX‐AQ K. Travis et al. 10.1029/2023JD039309
- Space-Based Observations of Ozone Precursors within California Wildfire Plumes and the Impacts on Ozone-NOx-VOC Chemistry X. Jin et al. 10.1021/acs.est.3c04411
- NEIVAv1.0: Next-generation Emissions InVentory expansion of Akagi et al. (2011) version 1.0 S. Binte Shahid et al. 10.5194/gmd-17-7679-2024
- Observational evidence reveals the significance of nocturnal chemistry in seasonal secondary organic aerosol formation L. Liu et al. 10.1038/s41612-024-00747-6
- Emissions and Atmospheric Chemistry of Furanoids from Biomass Burning: Insights from Laboratory to Atmospheric Observations M. Romanias et al. 10.1021/acsearthspacechem.3c00226
- Evolution of Reactive Organic Compounds and Their Potential Health Risk in Wildfire Smoke H. Pye et al. 10.1021/acs.est.4c06187
Latest update: 20 Nov 2024
Short summary
Fires emit many gases which can contribute to smog and air pollution. However, the amount and properties of these chemicals are not well understood, so this work updates and expands their representation in a global atmospheric model, including by adding new chemicals. We confirm that this updated representation generally matches measurements taken in several fire regions. We then show that fires provide ~15 % of atmospheric reactivity globally and more than 75 % over fire source regions.
Fires emit many gases which can contribute to smog and air pollution. However, the amount and...
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