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The impact of the 2016 Fort McMurray Horse River Wildfire on ambient air pollution levels in the Athabasca Oil Sands Region, Alberta, Canada.

Authors :
Landis MS
Edgerton ES
White EM
Wentworth GR
Sullivan AP
Dillner AM
Source :
The Science of the total environment [Sci Total Environ] 2018 Mar 15; Vol. 618, pp. 1665-1676. Date of Electronic Publication: 2017 Nov 04.
Publication Year :
2018

Abstract

An unprecedented wildfire impacted the northern Alberta city of Fort McMurray in May 2016 causing a mandatory city wide evacuation and the loss of 2,400 homes and commercial structures. A two-hectare wildfire was discovered on May 1, grew to ~157,000ha by May 5, and continued to burn an estimated ~590,000ha by June 13. A comprehensive air monitoring network operated by the Wood Buffalo Environmental Association (WBEA) in and around Fort McMurray provided essential health-related real-time air quality data to firefighters during the emergency, and provided a rare opportunity to elucidate the impact of gaseous and particulate matter emissions on near-field communities and regional air pollution concentrations. The WBEA network recorded 188 fire-related exceedances of 1-hr and 24-hr Alberta Ambient Air Quality Objectives. Two air monitoring sites within Fort McMurray recorded mean/maximum 1-hr PM <subscript>2.5</subscript> concentrations of 291/5229μgm <superscript>-3</superscript> (AMS-6) and 293/3259μgm <superscript>-3</superscript> (AMS-7) during fire impact periods. High correlations (r <superscript>2</superscript> =0.83-0.97) between biomass combustion related gases (carbon monoxide (CO), non-methane hydrocarbons (NMHC), total hydrocarbons (THC), total reduced sulfur (TRS), ammonia) and PM <subscript>2.5</subscript> were observed at the sites. Filter-based 24-hr integrated PM <subscript>2.5</subscript> samples collected every 6 days showed maximum concentrations of 267μgm <superscript>-3</superscript> (AMS-6) and 394μgm <superscript>-3</superscript> (AMS-7). Normalized excess emission ratios relative to CO were 149.87±3.37μgm <superscript>-3</superscript> ppm <superscript>-1</superscript> (PM <subscript>2.5</subscript> ), 0.274±0.002ppmppm <superscript>-1</superscript> (THC), 0.169±0.001ppmppm <superscript>-1</superscript> (NMHC), 0.104±0.001ppmppm <superscript>-1</superscript> (CH <subscript>4</subscript> ), 0.694±0.007ppbppm <superscript>-1</superscript> (TRS), 0.519±0.040ppbppm <superscript>-1</superscript> (SO <subscript>2</subscript> ), 0.412±0.045ppbppm <superscript>-1</superscript> (NO), 1.968±0.053ppbppm <superscript>-1</superscript> (NO <subscript>2</subscript> ), and 2.337±0.077ppbppm <superscript>-1</superscript> (NO <subscript>X</subscript> ). A subset of PM <subscript>2.5</subscript> filter samples was analyzed for trace elements, major ions, organic carbon, elemental carbon, and carbohydrates. Sample mass reconstruction and fire specific emission profiles are presented and discussed. Potential fire-related photometric ozone instrument positive interferences were observed and were positively correlated with NO and NMHC.<br /> (Published by Elsevier B.V.)

Details

Language :
English
ISSN :
1879-1026
Volume :
618
Database :
MEDLINE
Journal :
The Science of the total environment
Publication Type :
Academic Journal
Accession number :
29102183
Full Text :
https://doi.org/10.1016/j.scitotenv.2017.10.008