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Transport of forest fire emissions from Alaska and the Yukon Territory to Nova Scotia during summer 2004
被引:51
作者:

Duck, Thomas J.
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Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

Firanski, Bernard J.
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机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

Millet, Dylan B.
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机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

Goldstein, Allen H.
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机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

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Holzinger, Rupert
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机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

Worsnop, Douglas R.
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机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

White, Allen B.
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机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

Stohl, Andreas
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h-index: 0
机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

Dickinson, Cameron S.
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h-index: 0
机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada

van Donkelaar, Aaron
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h-index: 0
机构: Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada
机构:
[1] Dalhousie Univ, Dept Phys & Atmospher Sci, Halifax, NS B3H 3J5, Canada
[2] Univ Calif Berkeley, Div Ecosyst Sci, Berkeley, CA 94720 USA
[3] Univ Manchester, Sch Earth Atmospher & Environm Sci, Manchester M60 1QD, Lancs, England
[4] Aerodyne Res Inc, Billerica, MA 01821 USA
[5] Univ Colorado, Earth Syst Res Lab, Boulder, CO 80305 USA
[6] Norwegian Inst Air Res, N-2027 Kjeller, Norway
基金:
英国自然环境研究理事会;
关键词:
D O I:
10.1029/2006JD007716
中图分类号:
P4 [大气科学(气象学)];
学科分类号:
0706 ;
070601 ;
摘要:
[1] Emissions from forest fires in Alaska and the Yukon Territory were observed at Chebogue Point, Nova Scotia (43.7 degrees N, 66.1 degrees W), between 11 and 13 July 2004. Smoke aerosols were first detected in the free troposphere by a Raman lidar and extended up to 8 km altitude. The plume was not evident at the surface until the second day, when increases in CO, acetonitrile (CH3CN), benzene, and aerosol mass concentrations were observed by in situ instrumentation. Enhancement ratios for each species relative to CO agreed with the range of values from other measurements of the same plume. The surface aerosols had an elevated black carbon fraction relative to both CO and organic matter, and the ratio of black to organic carbon was higher than what is typically observed in fresh smoke. The emissions were tracked back to Alaska and the Yukon Territory using aerosol optical depth measurements from the Aqua MODIS satellite instrument, and the transport was reconstructed using the GEOS-Chem and FLEXPART atmospheric models. The analysis suggests that aerosols were injected into the atmosphere in proportion to CO and that aerosol removal processes were weak during the 7 to 9 day transit time in the free troposphere. Transport of the tracers to the ground was strongly connected to synoptic-scale features in the surface meteorology.
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