Journal of Geophysical Research Atmospheres · 2019 · 58 citations · 116 references
Natural SciencesEarth SciencesEnvironmental SciencesAtmospheric ChemistryAtmospheric ScienceClimatologyData AssimilationFire DynamicsFire WeatherRegional ClimatologyWildfire EcologyCarbon Monoxide DetectionFire Weather AssessmentFire-climate InteractionsSpectroscopic CharacterizationSpectroscopic DetectionWildfire DetectionWildfire EmissionsWildfire Monitoring
Abstract From 17–22 August 2017 simultaneous enhancements of ammonia (NH 3 ), carbon monoxide (CO), hydrogen cyanide (HCN), and ethane (C 2 H 6 ) were detected from ground‐based solar absorption Fourier transform infrared (FTIR) spectroscopic measurements at two high‐Arctic sites: Eureka (80.05°N, 86.42°W) Nunavut, Canada, and Thule (76.53°N, 68.74°W), Greenland. These enhancements were attributed to wildfires in British Columbia and the Northwest Territories of Canada using FLEXPART back‐trajectories and fire locations from Moderate Resolution Imaging Spectroradiometer (MODIS) and found to be the greatest observed enhancements in more than a decade of measurements at Eureka (2006–2017) and Thule (1999–2017). Observations of gas‐phase NH 3 from these wildfires illustrate that boreal wildfires may be a considerable episodic source of NH 3 in the summertime high Arctic. Comparisons of GEOS‐Chem model simulations using the Global Fire Assimilation System (GFASv1.2) biomass burning emissions to FTIR measurements and Infrared Atmospheric Sounding Interferometer (IASI) measurements showed that the transport of wildfire emissions to the Arctic was underestimated in GEOS‐Chem. However, GEOS‐Chem simulations showed that these wildfires contributed to surface layer NH 3 and NH enhancements of 0.01–0.11 ppbv and 0.05–1.07 ppbv, respectively, over the Canadian Archipelago from 15–23 August 2017.
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