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Title: Particulate Matter, Ozone, and Nitrogen Species in Aged Wildfire Plumes Observed at the Mount Bachelor Observatory

Journal Article · · Aerosol and Air Quality Research
 [1];  [2];  [3];  [3];  [2];  [4];  [4];  [4];  [5];  [6]
  1. Gradient, Seattle, WA (United States); Univ. of Washington, Seattle, WA (United States). Dept. of Atmospheric Sciences
  2. Univ. of Washington, Bothell, WA (United States). School of Science, Technology, Engineering and Mathematics; Univ. of Washington, Seattle, WA (United States). Dept. of Atmospheric Sciences
  3. Univ. of Washington, Bothell, WA (United States). School of Science, Technology, Engineering and Mathematics
  4. Univ. of California, Davis, CA (United States). Dept. of Environmental Toxicology
  5. Univ. of Washington, Seattle, WA (United States). Dept. of Statistics
  6. Sunset Lab., Inc., Tigard, OR (United States)

During the summer of 2012 and 2013, we measured carbon monoxide (CO), carbon dioxide (CO2), ozone (O3), nitrogen oxides (NOx), reactive nitrogen (NOy), peroxyacetyl nitrate (PAN), aerosol scattering (σsp) and absorption, elemental and organic carbon (EC and OC), and aerosol chemistry at the Mount Bachelor Observatory (2.8 km above sea level, Oregon, US). Here we analyze 23 of the individual plumes from regional wildfires to better understand production and loss of aerosols and gaseous species. We also developed a new method to calculate enhancement ratios and Modified Combustion Efficiency (MCE), which takes into account possible changes in background concentrations during transport. We compared this new method to existing methods for calculating enhancement ratios. The MCE values ranged from 0.79– 0.98, ΔO3/ΔCO ranged from 0.01–0.07 ppbv ppbv–1, Δσsp/ΔCO ranged from 0.23–1.32 Mm–1 (at STP) ppbv–1, ΔNOy/ΔCO ranged from 2.89–12.82 pptv ppbv–1, and ΔPAN/ΔCO ranged from 1.46–6.25 pptv ppbv–1. A comparison of three different methods to calculate enhancement ratios (ER) showed that the methods generally resulted in similar Δσsp/ΔCO, ΔNOy/ΔCO, and ΔPAN/ΔCO; however, there was a significant bias between the methods when calculating ΔO3/ΔCO due to the small absolute enhancement of O3 in the plumes. The ΔO3/ΔCO ERs calculated using two common methods were biased low (~20–30%) when compared to the new proposed method. Two pieces of evidence suggest moderate secondary particulate formation in many of the plumes studied: 1) mean observed ΔOC/ΔCO2 was 0.028 g particulate-C gC–1 (as CO2)—27% higher than the midpoint of the biomass burning emission ratio range reported by a recent review—and 2) single scattering albedo (ω) was relatively constant at all MCE values, in contrast with results for fresh plumes. Lastly, the observed NOx, PAN, and aerosol nitrate represented 6–48%, 25–57%, and 20–69% of the observed NOy in the aged plumes, respectively, and other species represented on average 11% of the observed NOy.

Research Organization:
Univ. of California, Davis, CA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Biological and Environmental Research (BER)
Grant/Contract Number:
SC0014620
OSTI ID:
1425944
Journal Information:
Aerosol and Air Quality Research, Vol. 16, Issue 12; ISSN 1680-8584
Publisher:
Chinese Association for Aerosol Research in TaiwanCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 44 works
Citation information provided by
Web of Science

Cited By (7)

Impact of Biomass Burning Plumes on Photolysis Rates and Ozone Formation at the Mount Bachelor Observatory journal February 2018
Physical and optical properties of aged biomass burning aerosol from wildfires in Siberia and the Western USA at the Mt. Bachelor Observatory journal January 2016
Regional influence of wildfires on aerosol chemistry in the western US and insights into atmospheric aging of biomass burning organic aerosol journal January 2017
Formation and evolution of tar balls from northwestern US wildfires journal January 2018
Using TES retrievals to investigate PAN in North American biomass burning plumes journal January 2018
Free tropospheric aerosols at the Mt. Bachelor Observatory: more oxidized and higher sulfate content compared to boundary layer aerosols journal January 2019
Free Tropospheric Aerosols at the Mt. Bachelor Observatory: More Oxidized and Higher Sulfate Content Compared to Boundary Layer Aerosols journal September 2018

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