Detection and Attribution of Wildfire Pollution in the Arctic

• Main Authors: Strong, K., Lutsch, E., Conway, S., Jones, D.B.A., Fisher, J.A., Ortega, I., Hannigan, J.W., Makarova, M., Palm, M., Notholt, J., Blumenstock, T., Sussmann, R., Mahieu, Emmanuel, Nagahama, T., Morino, I., Kasai, Y., Morris, E., Murphy, K., Evans, M.J.
• Format: Conference Object
• Language: English
• Published: 2019
• Subjects: remote-sensing; Polar atmosphere; Physical; chemical; mathematical & earth Sciences; Earth sciences & physical geography; Physique; chimie; mathématiques & sciences de la terre; Sciences de la terre & géographie physique; Arctic; Kiruna; Eureka
• Online Access: https://orbi.uliege.be/handle/2268/267530

The Arctic experiences poor air quality due to transport of pollutants from mid-latitudes, with wildfires providing an episodic source of trace gases and particulates. We present a multi-year time series of the total columns of CO, HCN, and C2H6 measured using Fourier transform infrared spectrometers at ten sites affiliated with the Network for Detection of Atmospheric Composition Change (NDACC). Six are high-latitude sites: Eureka, Ny Alesund, Thule, Kiruna, Poker Flat, and St. Petersburg, and four are mid-latitude sites: Zugspitze, Jungfraujoch, Toronto, and Rikubetsu. For each site, the inter-annual trends and seasonal variabilities of the CO total column time series are accounted for, allowing ambient concentrations to be determined. Enhancements above ambient levels are then used to identify possible wildfire pollution events. Since the abundance of each trace gas emitted in a wildfire event is specific to the type of vegetation burned and the burning phase, correlations of CO to the long-lived wildfire tracers HCN and C2H6 allow for further confirmation of the detection of wildfire pollution, while complementary measurements of aerosol optical depth from nearby AERONET sites confirms the presence of wildfire smoke. GEOS-Chem tagged CO simulations with Global Fire Assimilation System (GFAS) biomass burning emissions were used to determine the source attribution of CO concentrations at each site from 2003-2017. The influence of the various wildfire sources is found to differ between sites; however, North American and Eurasian boreal wildfires fires are found to be the greatest contributors to episodic CO enhancements in the summertime at all sites.