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Volume 13, issue 2 | Copyright

Special issue: Quantifying the impact of Boreal fires on tropospheric oxidants...

Atmos. Chem. Phys., 13, 851-867, 2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 22 Jan 2013

Research article | 22 Jan 2013

The influence of biomass burning on the global distribution of selected non-methane organic compounds

A. C. Lewis1, M. J. Evans1,2, J. R. Hopkins1, S. Punjabi2, K. A. Read1, R. M. Purvis1, S. J. Andrews2, S. J. Moller1, L. J. Carpenter2, J. D. Lee1, A. R. Rickard1, P. I. Palmer3, and M. Parrington3 A. C. Lewis et al.
  • 1National Centre for Atmospheric Science (NCAS), University of York, Heslington, York YO10 5DD, UK
  • 2Department of Chemistry, University of York, Heslington, York YO10 5DD, UK
  • 3School of Geosciences, University of Edinburgh, The King's Buildings, Edinburgh EH9 3JN, UK

Abstract. Forests fires are a significant source of chemicals to the atmosphere including numerous non-methane organic compounds (NMOCs). We report airborne measurement of hydrocarbons, acetone and methanol from >500 whole air samples collected over Eastern Canada, including interceptions of several different boreal biomass burning plumes. From these and concurrent measurements of carbon monoxide (CO) we derive fire emission ratios for 29 different organic species relative to the emission of CO. These range from 8.9 ± 3.2 ppt ppb−1 CO for methanol to 0.007 ± 0.004 ppt ppb−1 CO for cyclopentane. The ratios are in good to excellent agreement with literature values. Using the GEOS-Chem global 3-D chemical transport model (CTM) we show the influence of biomass burning on the global distributions of benzene, toluene, ethene and propene (species which are controlled for air quality purposes and sometimes used as indicative tracers of anthropogenic activity). Using our observationally derived emission ratios and the GEOS-Chem CTM, we show that biomass burning can be the largest fractional contributor to observed benzene, toluene, ethene and propene levels in many global locations. The widespread biomass burning contribution to atmospheric benzene, a heavily regulated air pollutant, suggests that pragmatic approaches are needed when setting air quality targets as tailpipe and solvent emissions decline in developed countries. We subsequently determine the extent to which the 28 global-status World Meteorological Organisation – Global Atmosphere Watch stations worldwide are influenced by biomass burning sourced benzene, toluene, ethene and propene as compared to their exposure to anthropogenic emissions.

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