The sensitivity of CO and aerosol transport to the temporal and vertical distribution of North American boreal fire emissions

Forest fires in Alaska and western Canada represent important sources of aerosols and trace gases in North America. Among the largest uncertainties when modeling forest fire effects are the timing and injection height of biomass burning emissions. Here we simulate CO and aerosols over North America...

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Published in:Atmospheric Chemistry and Physics
Main Authors: Chen, Y., Li, Q., Randerson, J. T., Lyons, E. A., Kahn, R. A., Nelson, D. L., Diner, D. J.
Format: Text
Language:English
Published: 2018
Subjects:
Online Access:https://doi.org/10.5194/acp-9-6559-2009
https://www.atmos-chem-phys.net/9/6559/2009/
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spelling ftcopernicus:oai:publications.copernicus.org:acp371 2023-05-15T16:35:31+02:00 The sensitivity of CO and aerosol transport to the temporal and vertical distribution of North American boreal fire emissions Chen, Y. Li, Q. Randerson, J. T. Lyons, E. A. Kahn, R. A. Nelson, D. L. Diner, D. J. 2018-01-15 application/pdf https://doi.org/10.5194/acp-9-6559-2009 https://www.atmos-chem-phys.net/9/6559/2009/ eng eng doi:10.5194/acp-9-6559-2009 https://www.atmos-chem-phys.net/9/6559/2009/ eISSN: 1680-7324 Text 2018 ftcopernicus https://doi.org/10.5194/acp-9-6559-2009 2019-12-24T09:57:45Z Forest fires in Alaska and western Canada represent important sources of aerosols and trace gases in North America. Among the largest uncertainties when modeling forest fire effects are the timing and injection height of biomass burning emissions. Here we simulate CO and aerosols over North America during the 2004 fire season, using the GEOS-Chem chemical transport model. We apply different temporal distributions and injection height profiles to the biomass burning emissions, and compare model results with satellite-, aircraft-, and ground-based measurements. We find that averaged over the fire season, the use of finer temporal resolved biomass burning emissions usually decreases CO and aerosol concentrations near the fire source region, and often enhances long-range transport. Among the individual temporal constraints, switching from monthly to 8-day time intervals for emissions has the largest effect on CO and aerosol distributions, and shows better agreement with measured day-to-day variability. Injection height substantially modifies the surface concentrations and vertical profiles of pollutants near the source region. Compared with CO, the simulation of black carbon aerosol is more sensitive to the temporal and injection height distribution of emissions. The use of MISR-derived injection heights improves agreement with surface aerosol measurements near the fire source. Our results indicate that the discrepancies between model simulations and MOPITT CO measurements near the Hudson Bay can not be attributed solely to the representation of injection height within the model. Frequent occurrence of strong convection in North America during summer tends to limit the influence of injection height parameterizations of fire emissions in Alaska and western Canada with respect to CO and aerosol distributions over eastern North America. Text Hudson Bay Alaska Copernicus Publications: E-Journals Canada Hudson Hudson Bay Atmospheric Chemistry and Physics 9 17 6559 6580
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collection Copernicus Publications: E-Journals
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language English
description Forest fires in Alaska and western Canada represent important sources of aerosols and trace gases in North America. Among the largest uncertainties when modeling forest fire effects are the timing and injection height of biomass burning emissions. Here we simulate CO and aerosols over North America during the 2004 fire season, using the GEOS-Chem chemical transport model. We apply different temporal distributions and injection height profiles to the biomass burning emissions, and compare model results with satellite-, aircraft-, and ground-based measurements. We find that averaged over the fire season, the use of finer temporal resolved biomass burning emissions usually decreases CO and aerosol concentrations near the fire source region, and often enhances long-range transport. Among the individual temporal constraints, switching from monthly to 8-day time intervals for emissions has the largest effect on CO and aerosol distributions, and shows better agreement with measured day-to-day variability. Injection height substantially modifies the surface concentrations and vertical profiles of pollutants near the source region. Compared with CO, the simulation of black carbon aerosol is more sensitive to the temporal and injection height distribution of emissions. The use of MISR-derived injection heights improves agreement with surface aerosol measurements near the fire source. Our results indicate that the discrepancies between model simulations and MOPITT CO measurements near the Hudson Bay can not be attributed solely to the representation of injection height within the model. Frequent occurrence of strong convection in North America during summer tends to limit the influence of injection height parameterizations of fire emissions in Alaska and western Canada with respect to CO and aerosol distributions over eastern North America.
format Text
author Chen, Y.
Li, Q.
Randerson, J. T.
Lyons, E. A.
Kahn, R. A.
Nelson, D. L.
Diner, D. J.
spellingShingle Chen, Y.
Li, Q.
Randerson, J. T.
Lyons, E. A.
Kahn, R. A.
Nelson, D. L.
Diner, D. J.
The sensitivity of CO and aerosol transport to the temporal and vertical distribution of North American boreal fire emissions
author_facet Chen, Y.
Li, Q.
Randerson, J. T.
Lyons, E. A.
Kahn, R. A.
Nelson, D. L.
Diner, D. J.
author_sort Chen, Y.
title The sensitivity of CO and aerosol transport to the temporal and vertical distribution of North American boreal fire emissions
title_short The sensitivity of CO and aerosol transport to the temporal and vertical distribution of North American boreal fire emissions
title_full The sensitivity of CO and aerosol transport to the temporal and vertical distribution of North American boreal fire emissions
title_fullStr The sensitivity of CO and aerosol transport to the temporal and vertical distribution of North American boreal fire emissions
title_full_unstemmed The sensitivity of CO and aerosol transport to the temporal and vertical distribution of North American boreal fire emissions
title_sort sensitivity of co and aerosol transport to the temporal and vertical distribution of north american boreal fire emissions
publishDate 2018
url https://doi.org/10.5194/acp-9-6559-2009
https://www.atmos-chem-phys.net/9/6559/2009/
geographic Canada
Hudson
Hudson Bay
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Hudson
Hudson Bay
genre Hudson Bay
Alaska
genre_facet Hudson Bay
Alaska
op_source eISSN: 1680-7324
op_relation doi:10.5194/acp-9-6559-2009
https://www.atmos-chem-phys.net/9/6559/2009/
op_doi https://doi.org/10.5194/acp-9-6559-2009
container_title Atmospheric Chemistry and Physics
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