1Department of Physics, University of Toronto, Toronto, ON, Canada
2National Center for Atmospheric Research, Boulder, CO, USA
3Department of Chemistry, University of Wollongong, Wollongong, New South Wales, Australia
4Department of Earth and Environmental Sciences, University of Waterloo, Waterloo, ON, Canada
5Department of Atmospheric Sciences, University of Utah, Salt Lake City, UT, USA
*now at: Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA, USA
**now at: School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA
Received: 09 Aug 2014 – Published in Atmos. Chem. Phys. Discuss.: 21 Oct 2014
Abstract. We investigate Arctic tropospheric composition using ground-based Fourier transform infrared (FTIR) solar absorption spectra, recorded at the Polar Environment Atmospheric Research Laboratory (PEARL, Eureka, Nunavut, Canada, 80°05' N, 86°42' W) and at Thule (Greenland, 76°53' N, −68°74' W) from 2008 to 2012. The target species, carbon monoxide (CO), hydrogen cyanide (HCN), ethane (C2H6), acetylene (C2H2), formic acid (HCOOH), and formaldehyde (H2CO) are emitted by biomass burning and can be transported from mid-latitudes to the Arctic.
Revised: 28 Jan 2015 – Accepted: 30 Jan 2015 – Published: 02 Mar 2015
By detecting simultaneous enhancements of three biomass burning tracers (HCN, CO, and C2H6), ten and eight fire events are identified at Eureka and Thule, respectively, within the 5-year FTIR time series. Analyses of Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT) model back-trajectories coupled with Moderate Resolution Imaging Spectroradiometer (MODIS) fire hotspot data, Stochastic Time-Inverted Lagrangian Transport (STILT) model footprints, and Ozone Monitoring Instrument (OMI) UV aerosol index maps, are used to attribute burning source regions and travel time durations of the plumes. By taking into account the effect of aging of the smoke plumes, measured FTIR enhancement ratios were corrected to obtain emission ratios and equivalent emission factors. The means of emission factors for extratropical forest estimated with the two FTIR data sets are 0.40 ± 0.21 g kg−1 for HCN, 1.24 ± 0.71 g kg−1 for C2H6, 0.34 ± 0.21 g kg−1 for C2H2, and 2.92 ± 1.30 g kg−1 for HCOOH. The emission factor for CH3OH estimated at Eureka is 3.44 ± 1.68 g kg−1.
To improve our knowledge concerning the dynamical and chemical processes associated with Arctic pollution from fires, the two sets of FTIR measurements were compared to the Model for OZone And Related chemical Tracers, version 4 (MOZART-4). Seasonal cycles and day-to-day variabilities were compared to assess the ability of the model to reproduce emissions from fires and their transport. Good agreement in winter confirms that transport is well implemented in the model. For C2H6, however, the lower wintertime concentration estimated by the model as compared to the FTIR observations highlights an underestimation of its emission. Results show that modeled and measured total columns are correlated (linear correlation coefficient r > 0.6 for all gases except for H2CO at Eureka and HCOOH at Thule), but suggest a general underestimation of the concentrations in the model for all seven tropospheric species in the high Arctic.
Viatte, C., Strong, K., Hannigan, J., Nussbaumer, E., Emmons, L. K., Conway, S., Paton-Walsh, C., Hartley, J., Benmergui, J., and Lin, J.: Identifying fire plumes in the Arctic with tropospheric FTIR measurements and transport models, Atmos. Chem. Phys., 15, 2227-2246, doi:10.5194/acp-15-2227-2015, 2015.