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Significant enhancements of nitrogen oxides, black carbon, and ozone in the North Atlantic lower free troposphere resulting from North American boreal wildfires

Identifieur interne : 000143 ( PascalFrancis/Corpus ); précédent : 000142; suivant : 000144

Significant enhancements of nitrogen oxides, black carbon, and ozone in the North Atlantic lower free troposphere resulting from North American boreal wildfires

Auteurs : M. Val Martin ; R. E. Honrath ; R. C. Owen ; G. Pfister ; P. Fialho ; F. Barata

Source :

RBID : Pascal:07-0066720

Descripteurs français

English descriptors

Abstract

[1] Extensive wildfires burned in northern North America during summer 2004, releasing large amounts of trace gases and aerosols into the atmosphere. Emissions from these wildfires frequently impacted the PICO-NARE station, a mountaintop site situated 6-15 days downwind from the fires in the Azores Islands. To assess the impacts of the boreal wildfire emissions on the levels of aerosol black carbon (BC), nitrogen oxides and O3 downwind from North America, we analyzed measurements of CO, BC, total reactive nitrogen oxides (NOy), NOx (NO + NO2) and O3 made from June to September 2004 in combination with MOZART chemical transport model simulations. Long-range transport of boreal wildfire emissions resulted in large enhancements of CO, BC, NOy and NOx, with levels up to 250 ppbv, 665 ng m-3, 1100 pptv and 135 pptv, respectively. Enhancement ratios relative to CO were variable in the plumes sampled, most likely because of variations in wildfire emissions and removal processes during transport. Analyses of ABC/ACO, ΔNOy/ΔCO and ΔNOx/ΔCO ratios indicate that NOy and BC were on average efficiently exported in these plumes and suggest that decomposition of PAN to NOx was a significant source of NOx. High levels of NOx suggest continuing formation of O3 in these well-aged plumes. O3 levels were also significantly enhanced in the plumes, reaching up to 75 ppbv. Analysis of ΔO3/ΔCO ratios showed distinct behaviors of O3 in the plumes, which varied from significant to lower O3 production. We identify several potential reasons for the complex effects of boreal wildfire emissions on O3 and conclude that this behavior needs to be explored further in the future. These observations demonstrate that boreal wildfire emissions significantly contributed to the NOx and O3 budgets in the central North Atlantic lower free troposphere during summer 2004 and imply large-scale impacts on direct radiative forcing of the atmosphere and on tropospheric NOx and O3.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

pA  
A01 01  1    @0 0148-0227
A03   1    @0 J. geophys. res.
A05       @2 111
A06       @2 D23
A08 01  1  ENG  @1 Significant enhancements of nitrogen oxides, black carbon, and ozone in the North Atlantic lower free troposphere resulting from North American boreal wildfires
A11 01  1    @1 VAL MARTIN (M.)
A11 02  1    @1 HONRATH (R. E.)
A11 03  1    @1 OWEN (R. C.)
A11 04  1    @1 PFISTER (G.)
A11 05  1    @1 FIALHO (P.)
A11 06  1    @1 BARATA (F.)
A14 01      @1 Department of Civil and Environmental Engineering, Michigan Technological University @2 Houghton, Michigan @3 USA @Z 1 aut. @Z 2 aut. @Z 3 aut.
A14 02      @1 Atmospheric Chemistry Division, National Center for Atmospheric Research @2 Boulder, Colorado @3 USA @Z 4 aut.
A14 03      @1 Group of Chemistry and Physics of the Atmosphere, University of the Azores @2 Terra Cha @3 PRT @Z 5 aut. @Z 6 aut.
A20       @2 D23S60.1-D23S60.17
A21       @1 2006
A23 01      @0 ENG
A43 01      @1 INIST @2 3144 @5 354000145302170450
A44       @0 0000 @1 © 2007 INIST-CNRS. All rights reserved.
A45       @0 1 p.3/4
A47 01  1    @0 07-0066720
A60       @1 P
A61       @0 A
A64 01  1    @0 Journal of geophysical research
A66 01      @0 USA
C01 01    ENG  @0 [1] Extensive wildfires burned in northern North America during summer 2004, releasing large amounts of trace gases and aerosols into the atmosphere. Emissions from these wildfires frequently impacted the PICO-NARE station, a mountaintop site situated 6-15 days downwind from the fires in the Azores Islands. To assess the impacts of the boreal wildfire emissions on the levels of aerosol black carbon (BC), nitrogen oxides and O3 downwind from North America, we analyzed measurements of CO, BC, total reactive nitrogen oxides (NOy), NOx (NO + NO2) and O3 made from June to September 2004 in combination with MOZART chemical transport model simulations. Long-range transport of boreal wildfire emissions resulted in large enhancements of CO, BC, NOy and NOx, with levels up to 250 ppbv, 665 ng m-3, 1100 pptv and 135 pptv, respectively. Enhancement ratios relative to CO were variable in the plumes sampled, most likely because of variations in wildfire emissions and removal processes during transport. Analyses of ABC/ACO, ΔNOy/ΔCO and ΔNOx/ΔCO ratios indicate that NOy and BC were on average efficiently exported in these plumes and suggest that decomposition of PAN to NOx was a significant source of NOx. High levels of NOx suggest continuing formation of O3 in these well-aged plumes. O3 levels were also significantly enhanced in the plumes, reaching up to 75 ppbv. Analysis of ΔO3/ΔCO ratios showed distinct behaviors of O3 in the plumes, which varied from significant to lower O3 production. We identify several potential reasons for the complex effects of boreal wildfire emissions on O3 and conclude that this behavior needs to be explored further in the future. These observations demonstrate that boreal wildfire emissions significantly contributed to the NOx and O3 budgets in the central North Atlantic lower free troposphere during summer 2004 and imply large-scale impacts on direct radiative forcing of the atmosphere and on tropospheric NOx and O3.
C02 01  2    @0 220
C02 02  3    @0 001E
C02 03  2    @0 001E01
C03 01  2  FRE  @0 Oxyde azote @5 01
C03 01  2  ENG  @0 nitrogen oxide @5 01
C03 02  X  FRE  @0 Azote oxyde @5 02
C03 02  X  ENG  @0 Nitrogen oxide @5 02
C03 02  X  SPA  @0 Nitrógeno óxido @5 02
C03 03  X  FRE  @0 Suie @5 03
C03 03  X  ENG  @0 Soot @5 03
C03 03  X  SPA  @0 Hollín @5 03
C03 04  2  FRE  @0 Ozone @5 04
C03 04  2  ENG  @0 ozone @5 04
C03 04  2  SPA  @0 Ozono @5 04
C03 05  2  FRE  @0 Troposphère @5 05
C03 05  2  ENG  @0 troposphere @5 05
C03 06  2  FRE  @0 Boréal @5 06
C03 06  2  ENG  @0 Boreal @5 06
C03 06  2  SPA  @0 Boreal @5 06
C03 07  2  FRE  @0 Amérique du Nord @5 07
C03 07  2  ENG  @0 North America @5 07
C03 07  2  SPA  @0 America del norte @5 07
C03 08  X  FRE  @0 Eté @5 08
C03 08  X  ENG  @0 Summer @5 08
C03 08  X  SPA  @0 Verano @5 08
C03 09  X  FRE  @0 Composé trace @5 09
C03 09  X  ENG  @0 Trace compound @5 09
C03 09  X  SPA  @0 Compuesto huella @5 09
C03 10  2  FRE  @0 Aérosol @5 10
C03 10  2  ENG  @0 aerosols @5 10
C03 10  2  SPA  @0 Aerosol @5 10
C03 11  2  FRE  @0 Atmosphère @5 11
C03 11  2  ENG  @0 atmosphere @5 11
C03 11  2  SPA  @0 Atmósfera @5 11
C03 12  2  FRE  @0 Incendie @5 12
C03 12  2  ENG  @0 fires @5 12
C03 13  2  FRE  @0 Ile @5 13
C03 13  2  ENG  @0 islands @5 13
C03 13  2  SPA  @0 Isla @5 13
C03 14  3  FRE  @0 Transport grande distance @5 14
C03 14  3  ENG  @0 Long-range transport @5 14
C03 15  2  FRE  @0 Modèle @5 15
C03 15  2  ENG  @0 models @5 15
C03 15  2  SPA  @0 Modelo @5 15
C03 16  2  FRE  @0 Simulation @5 16
C03 16  2  ENG  @0 simulation @5 16
C03 16  2  SPA  @0 Simulación @5 16
C03 17  2  FRE  @0 Panache @5 17
C03 17  2  ENG  @0 plumes @5 17
C03 17  2  SPA  @0 Penacho @5 17
C03 18  2  FRE  @0 Exportation @5 18
C03 18  2  ENG  @0 export @5 18
C03 18  2  SPA  @0 Exportación @5 18
C03 19  X  FRE  @0 Transfert radiatif @5 19
C03 19  X  ENG  @0 Radiative transfer @5 19
C03 19  X  SPA  @0 Transferencia radiativa @5 19
C03 20  X  FRE  @0 Forçage @5 20
C03 20  X  ENG  @0 Forcing @5 20
C03 20  X  SPA  @0 Forzamiento @5 20
C03 21  2  FRE  @0 Océan Atlantique Nord @2 NG @5 61
C03 21  2  ENG  @0 North Atlantic @2 NG @5 61
C03 21  2  SPA  @0 Océano Atlántico Norte @2 NG @5 61
C03 22  2  FRE  @0 Açores @2 NG @5 62
C03 22  2  ENG  @0 Azores @2 NG @5 62
C03 22  2  SPA  @0 Azores @2 NG @5 62
C07 01  2  FRE  @0 Océan Atlantique
C07 01  2  ENG  @0 Atlantic Ocean
C07 01  2  SPA  @0 Océano Atlántico
C07 02  2  FRE  @0 Iles Océan Atlantique
C07 02  2  ENG  @0 Atlantic Ocean Islands
N21       @1 043
N44 01      @1 OTO
N82       @1 OTO

Format Inist (serveur)

NO : PASCAL 07-0066720 INIST
ET : Significant enhancements of nitrogen oxides, black carbon, and ozone in the North Atlantic lower free troposphere resulting from North American boreal wildfires
AU : VAL MARTIN (M.); HONRATH (R. E.); OWEN (R. C.); PFISTER (G.); FIALHO (P.); BARATA (F.)
AF : Department of Civil and Environmental Engineering, Michigan Technological University/Houghton, Michigan/Etats-Unis (1 aut., 2 aut., 3 aut.); Atmospheric Chemistry Division, National Center for Atmospheric Research/Boulder, Colorado/Etats-Unis (4 aut.); Group of Chemistry and Physics of the Atmosphere, University of the Azores/Terra Cha/Portugal (5 aut., 6 aut.)
DT : Publication en série; Niveau analytique
SO : Journal of geophysical research; ISSN 0148-0227; Etats-Unis; Da. 2006; Vol. 111; No. D23; D23S60.1-D23S60.17; Bibl. 1 p.3/4
LA : Anglais
EA : [1] Extensive wildfires burned in northern North America during summer 2004, releasing large amounts of trace gases and aerosols into the atmosphere. Emissions from these wildfires frequently impacted the PICO-NARE station, a mountaintop site situated 6-15 days downwind from the fires in the Azores Islands. To assess the impacts of the boreal wildfire emissions on the levels of aerosol black carbon (BC), nitrogen oxides and O3 downwind from North America, we analyzed measurements of CO, BC, total reactive nitrogen oxides (NOy), NOx (NO + NO2) and O3 made from June to September 2004 in combination with MOZART chemical transport model simulations. Long-range transport of boreal wildfire emissions resulted in large enhancements of CO, BC, NOy and NOx, with levels up to 250 ppbv, 665 ng m-3, 1100 pptv and 135 pptv, respectively. Enhancement ratios relative to CO were variable in the plumes sampled, most likely because of variations in wildfire emissions and removal processes during transport. Analyses of ABC/ACO, ΔNOy/ΔCO and ΔNOx/ΔCO ratios indicate that NOy and BC were on average efficiently exported in these plumes and suggest that decomposition of PAN to NOx was a significant source of NOx. High levels of NOx suggest continuing formation of O3 in these well-aged plumes. O3 levels were also significantly enhanced in the plumes, reaching up to 75 ppbv. Analysis of ΔO3/ΔCO ratios showed distinct behaviors of O3 in the plumes, which varied from significant to lower O3 production. We identify several potential reasons for the complex effects of boreal wildfire emissions on O3 and conclude that this behavior needs to be explored further in the future. These observations demonstrate that boreal wildfire emissions significantly contributed to the NOx and O3 budgets in the central North Atlantic lower free troposphere during summer 2004 and imply large-scale impacts on direct radiative forcing of the atmosphere and on tropospheric NOx and O3.
CC : 220; 001E; 001E01
FD : Oxyde azote; Azote oxyde; Suie; Ozone; Troposphère; Boréal; Amérique du Nord; Eté; Composé trace; Aérosol; Atmosphère; Incendie; Ile; Transport grande distance; Modèle; Simulation; Panache; Exportation; Transfert radiatif; Forçage; Océan Atlantique Nord; Açores
FG : Océan Atlantique; Iles Océan Atlantique
ED : nitrogen oxide; Nitrogen oxide; Soot; ozone; troposphere; Boreal; North America; Summer; Trace compound; aerosols; atmosphere; fires; islands; Long-range transport; models; simulation; plumes; export; Radiative transfer; Forcing; North Atlantic; Azores
EG : Atlantic Ocean; Atlantic Ocean Islands
SD : Nitrógeno óxido; Hollín; Ozono; Boreal; America del norte; Verano; Compuesto huella; Aerosol; Atmósfera; Isla; Modelo; Simulación; Penacho; Exportación; Transferencia radiativa; Forzamiento; Océano Atlántico Norte; Azores
LO : INIST-3144.354000145302170450
ID : 07-0066720

Links to Exploration step

Pascal:07-0066720

Le document en format XML

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<term>Nitrogen oxide</term>
<term>North America</term>
<term>North Atlantic</term>
<term>Radiative transfer</term>
<term>Soot</term>
<term>Summer</term>
<term>Trace compound</term>
<term>aerosols</term>
<term>atmosphere</term>
<term>export</term>
<term>fires</term>
<term>islands</term>
<term>models</term>
<term>nitrogen oxide</term>
<term>ozone</term>
<term>plumes</term>
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<term>Oxyde azote</term>
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<term>Incendie</term>
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<term>Transport grande distance</term>
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<term>Panache</term>
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<div type="abstract" xml:lang="en">[1] Extensive wildfires burned in northern North America during summer 2004, releasing large amounts of trace gases and aerosols into the atmosphere. Emissions from these wildfires frequently impacted the PICO-NARE station, a mountaintop site situated 6-15 days downwind from the fires in the Azores Islands. To assess the impacts of the boreal wildfire emissions on the levels of aerosol black carbon (BC), nitrogen oxides and O
<sub>3</sub>
downwind from North America, we analyzed measurements of CO, BC, total reactive nitrogen oxides (NOy), NO
<sub>x</sub>
(NO + NO
<sub>2</sub>
) and O
<sub>3</sub>
made from June to September 2004 in combination with MOZART chemical transport model simulations. Long-range transport of boreal wildfire emissions resulted in large enhancements of CO, BC, NO
<sub>y</sub>
and NO
<sub>x</sub>
, with levels up to 250 ppbv, 665 ng m
<sup>-3</sup>
, 1100 pptv and 135 pptv, respectively. Enhancement ratios relative to CO were variable in the plumes sampled, most likely because of variations in wildfire emissions and removal processes during transport. Analyses of ABC/ACO, ΔNO
<sub>y</sub>
/ΔCO and ΔNO
<sub>x</sub>
/ΔCO ratios indicate that NO
<sub>y</sub>
and BC were on average efficiently exported in these plumes and suggest that decomposition of PAN to NO
<sub>x</sub>
was a significant source of NO
<sub>x</sub>
. High levels of NO
<sub>x</sub>
suggest continuing formation of O
<sub>3</sub>
in these well-aged plumes. O
<sub>3</sub>
levels were also significantly enhanced in the plumes, reaching up to 75 ppbv. Analysis of ΔO
<sub>3</sub>
/ΔCO ratios showed distinct behaviors of O
<sub>3</sub>
in the plumes, which varied from significant to lower O
<sub>3</sub>
production. We identify several potential reasons for the complex effects of boreal wildfire emissions on O
<sub>3</sub>
and conclude that this behavior needs to be explored further in the future. These observations demonstrate that boreal wildfire emissions significantly contributed to the NO
<sub>x</sub>
and O
<sub>3</sub>
budgets in the central North Atlantic lower free troposphere during summer 2004 and imply large-scale impacts on direct radiative forcing of the atmosphere and on tropospheric NO
<sub>x</sub>
and O
<sub>3</sub>
.</div>
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</fA06>
<fA08 i1="01" i2="1" l="ENG">
<s1>Significant enhancements of nitrogen oxides, black carbon, and ozone in the North Atlantic lower free troposphere resulting from North American boreal wildfires</s1>
</fA08>
<fA11 i1="01" i2="1">
<s1>VAL MARTIN (M.)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>HONRATH (R. E.)</s1>
</fA11>
<fA11 i1="03" i2="1">
<s1>OWEN (R. C.)</s1>
</fA11>
<fA11 i1="04" i2="1">
<s1>PFISTER (G.)</s1>
</fA11>
<fA11 i1="05" i2="1">
<s1>FIALHO (P.)</s1>
</fA11>
<fA11 i1="06" i2="1">
<s1>BARATA (F.)</s1>
</fA11>
<fA14 i1="01">
<s1>Department of Civil and Environmental Engineering, Michigan Technological University</s1>
<s2>Houghton, Michigan</s2>
<s3>USA</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Atmospheric Chemistry Division, National Center for Atmospheric Research</s1>
<s2>Boulder, Colorado</s2>
<s3>USA</s3>
<sZ>4 aut.</sZ>
</fA14>
<fA14 i1="03">
<s1>Group of Chemistry and Physics of the Atmosphere, University of the Azores</s1>
<s2>Terra Cha</s2>
<s3>PRT</s3>
<sZ>5 aut.</sZ>
<sZ>6 aut.</sZ>
</fA14>
<fA20>
<s2>D23S60.1-D23S60.17</s2>
</fA20>
<fA21>
<s1>2006</s1>
</fA21>
<fA23 i1="01">
<s0>ENG</s0>
</fA23>
<fA43 i1="01">
<s1>INIST</s1>
<s2>3144</s2>
<s5>354000145302170450</s5>
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<fA44>
<s0>0000</s0>
<s1>© 2007 INIST-CNRS. All rights reserved.</s1>
</fA44>
<fA45>
<s0>1 p.3/4</s0>
</fA45>
<fA47 i1="01" i2="1">
<s0>07-0066720</s0>
</fA47>
<fA60>
<s1>P</s1>
</fA60>
<fA61>
<s0>A</s0>
</fA61>
<fA64 i1="01" i2="1">
<s0>Journal of geophysical research</s0>
</fA64>
<fA66 i1="01">
<s0>USA</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>[1] Extensive wildfires burned in northern North America during summer 2004, releasing large amounts of trace gases and aerosols into the atmosphere. Emissions from these wildfires frequently impacted the PICO-NARE station, a mountaintop site situated 6-15 days downwind from the fires in the Azores Islands. To assess the impacts of the boreal wildfire emissions on the levels of aerosol black carbon (BC), nitrogen oxides and O
<sub>3</sub>
downwind from North America, we analyzed measurements of CO, BC, total reactive nitrogen oxides (NOy), NO
<sub>x</sub>
(NO + NO
<sub>2</sub>
) and O
<sub>3</sub>
made from June to September 2004 in combination with MOZART chemical transport model simulations. Long-range transport of boreal wildfire emissions resulted in large enhancements of CO, BC, NO
<sub>y</sub>
and NO
<sub>x</sub>
, with levels up to 250 ppbv, 665 ng m
<sup>-3</sup>
, 1100 pptv and 135 pptv, respectively. Enhancement ratios relative to CO were variable in the plumes sampled, most likely because of variations in wildfire emissions and removal processes during transport. Analyses of ABC/ACO, ΔNO
<sub>y</sub>
/ΔCO and ΔNO
<sub>x</sub>
/ΔCO ratios indicate that NO
<sub>y</sub>
and BC were on average efficiently exported in these plumes and suggest that decomposition of PAN to NO
<sub>x</sub>
was a significant source of NO
<sub>x</sub>
. High levels of NO
<sub>x</sub>
suggest continuing formation of O
<sub>3</sub>
in these well-aged plumes. O
<sub>3</sub>
levels were also significantly enhanced in the plumes, reaching up to 75 ppbv. Analysis of ΔO
<sub>3</sub>
/ΔCO ratios showed distinct behaviors of O
<sub>3</sub>
in the plumes, which varied from significant to lower O
<sub>3</sub>
production. We identify several potential reasons for the complex effects of boreal wildfire emissions on O
<sub>3</sub>
and conclude that this behavior needs to be explored further in the future. These observations demonstrate that boreal wildfire emissions significantly contributed to the NO
<sub>x</sub>
and O
<sub>3</sub>
budgets in the central North Atlantic lower free troposphere during summer 2004 and imply large-scale impacts on direct radiative forcing of the atmosphere and on tropospheric NO
<sub>x</sub>
and O
<sub>3</sub>
.</s0>
</fC01>
<fC02 i1="01" i2="2">
<s0>220</s0>
</fC02>
<fC02 i1="02" i2="3">
<s0>001E</s0>
</fC02>
<fC02 i1="03" i2="2">
<s0>001E01</s0>
</fC02>
<fC03 i1="01" i2="2" l="FRE">
<s0>Oxyde azote</s0>
<s5>01</s5>
</fC03>
<fC03 i1="01" i2="2" l="ENG">
<s0>nitrogen oxide</s0>
<s5>01</s5>
</fC03>
<fC03 i1="02" i2="X" l="FRE">
<s0>Azote oxyde</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="ENG">
<s0>Nitrogen oxide</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="X" l="SPA">
<s0>Nitrógeno óxido</s0>
<s5>02</s5>
</fC03>
<fC03 i1="03" i2="X" l="FRE">
<s0>Suie</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="ENG">
<s0>Soot</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="X" l="SPA">
<s0>Hollín</s0>
<s5>03</s5>
</fC03>
<fC03 i1="04" i2="2" l="FRE">
<s0>Ozone</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="2" l="ENG">
<s0>ozone</s0>
<s5>04</s5>
</fC03>
<fC03 i1="04" i2="2" l="SPA">
<s0>Ozono</s0>
<s5>04</s5>
</fC03>
<fC03 i1="05" i2="2" l="FRE">
<s0>Troposphère</s0>
<s5>05</s5>
</fC03>
<fC03 i1="05" i2="2" l="ENG">
<s0>troposphere</s0>
<s5>05</s5>
</fC03>
<fC03 i1="06" i2="2" l="FRE">
<s0>Boréal</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="2" l="ENG">
<s0>Boreal</s0>
<s5>06</s5>
</fC03>
<fC03 i1="06" i2="2" l="SPA">
<s0>Boreal</s0>
<s5>06</s5>
</fC03>
<fC03 i1="07" i2="2" l="FRE">
<s0>Amérique du Nord</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="2" l="ENG">
<s0>North America</s0>
<s5>07</s5>
</fC03>
<fC03 i1="07" i2="2" l="SPA">
<s0>America del norte</s0>
<s5>07</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Eté</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Summer</s0>
<s5>08</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Verano</s0>
<s5>08</s5>
</fC03>
<fC03 i1="09" i2="X" l="FRE">
<s0>Composé trace</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="ENG">
<s0>Trace compound</s0>
<s5>09</s5>
</fC03>
<fC03 i1="09" i2="X" l="SPA">
<s0>Compuesto huella</s0>
<s5>09</s5>
</fC03>
<fC03 i1="10" i2="2" l="FRE">
<s0>Aérosol</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="2" l="ENG">
<s0>aerosols</s0>
<s5>10</s5>
</fC03>
<fC03 i1="10" i2="2" l="SPA">
<s0>Aerosol</s0>
<s5>10</s5>
</fC03>
<fC03 i1="11" i2="2" l="FRE">
<s0>Atmosphère</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="2" l="ENG">
<s0>atmosphere</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="2" l="SPA">
<s0>Atmósfera</s0>
<s5>11</s5>
</fC03>
<fC03 i1="12" i2="2" l="FRE">
<s0>Incendie</s0>
<s5>12</s5>
</fC03>
<fC03 i1="12" i2="2" l="ENG">
<s0>fires</s0>
<s5>12</s5>
</fC03>
<fC03 i1="13" i2="2" l="FRE">
<s0>Ile</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="2" l="ENG">
<s0>islands</s0>
<s5>13</s5>
</fC03>
<fC03 i1="13" i2="2" l="SPA">
<s0>Isla</s0>
<s5>13</s5>
</fC03>
<fC03 i1="14" i2="3" l="FRE">
<s0>Transport grande distance</s0>
<s5>14</s5>
</fC03>
<fC03 i1="14" i2="3" l="ENG">
<s0>Long-range transport</s0>
<s5>14</s5>
</fC03>
<fC03 i1="15" i2="2" l="FRE">
<s0>Modèle</s0>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="2" l="ENG">
<s0>models</s0>
<s5>15</s5>
</fC03>
<fC03 i1="15" i2="2" l="SPA">
<s0>Modelo</s0>
<s5>15</s5>
</fC03>
<fC03 i1="16" i2="2" l="FRE">
<s0>Simulation</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="2" l="ENG">
<s0>simulation</s0>
<s5>16</s5>
</fC03>
<fC03 i1="16" i2="2" l="SPA">
<s0>Simulación</s0>
<s5>16</s5>
</fC03>
<fC03 i1="17" i2="2" l="FRE">
<s0>Panache</s0>
<s5>17</s5>
</fC03>
<fC03 i1="17" i2="2" l="ENG">
<s0>plumes</s0>
<s5>17</s5>
</fC03>
<fC03 i1="17" i2="2" l="SPA">
<s0>Penacho</s0>
<s5>17</s5>
</fC03>
<fC03 i1="18" i2="2" l="FRE">
<s0>Exportation</s0>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="2" l="ENG">
<s0>export</s0>
<s5>18</s5>
</fC03>
<fC03 i1="18" i2="2" l="SPA">
<s0>Exportación</s0>
<s5>18</s5>
</fC03>
<fC03 i1="19" i2="X" l="FRE">
<s0>Transfert radiatif</s0>
<s5>19</s5>
</fC03>
<fC03 i1="19" i2="X" l="ENG">
<s0>Radiative transfer</s0>
<s5>19</s5>
</fC03>
<fC03 i1="19" i2="X" l="SPA">
<s0>Transferencia radiativa</s0>
<s5>19</s5>
</fC03>
<fC03 i1="20" i2="X" l="FRE">
<s0>Forçage</s0>
<s5>20</s5>
</fC03>
<fC03 i1="20" i2="X" l="ENG">
<s0>Forcing</s0>
<s5>20</s5>
</fC03>
<fC03 i1="20" i2="X" l="SPA">
<s0>Forzamiento</s0>
<s5>20</s5>
</fC03>
<fC03 i1="21" i2="2" l="FRE">
<s0>Océan Atlantique Nord</s0>
<s2>NG</s2>
<s5>61</s5>
</fC03>
<fC03 i1="21" i2="2" l="ENG">
<s0>North Atlantic</s0>
<s2>NG</s2>
<s5>61</s5>
</fC03>
<fC03 i1="21" i2="2" l="SPA">
<s0>Océano Atlántico Norte</s0>
<s2>NG</s2>
<s5>61</s5>
</fC03>
<fC03 i1="22" i2="2" l="FRE">
<s0>Açores</s0>
<s2>NG</s2>
<s5>62</s5>
</fC03>
<fC03 i1="22" i2="2" l="ENG">
<s0>Azores</s0>
<s2>NG</s2>
<s5>62</s5>
</fC03>
<fC03 i1="22" i2="2" l="SPA">
<s0>Azores</s0>
<s2>NG</s2>
<s5>62</s5>
</fC03>
<fC07 i1="01" i2="2" l="FRE">
<s0>Océan Atlantique</s0>
</fC07>
<fC07 i1="01" i2="2" l="ENG">
<s0>Atlantic Ocean</s0>
</fC07>
<fC07 i1="01" i2="2" l="SPA">
<s0>Océano Atlántico</s0>
</fC07>
<fC07 i1="02" i2="2" l="FRE">
<s0>Iles Océan Atlantique</s0>
</fC07>
<fC07 i1="02" i2="2" l="ENG">
<s0>Atlantic Ocean Islands</s0>
</fC07>
<fN21>
<s1>043</s1>
</fN21>
<fN44 i1="01">
<s1>OTO</s1>
</fN44>
<fN82>
<s1>OTO</s1>
</fN82>
</pA>
</standard>
<server>
<NO>PASCAL 07-0066720 INIST</NO>
<ET>Significant enhancements of nitrogen oxides, black carbon, and ozone in the North Atlantic lower free troposphere resulting from North American boreal wildfires</ET>
<AU>VAL MARTIN (M.); HONRATH (R. E.); OWEN (R. C.); PFISTER (G.); FIALHO (P.); BARATA (F.)</AU>
<AF>Department of Civil and Environmental Engineering, Michigan Technological University/Houghton, Michigan/Etats-Unis (1 aut., 2 aut., 3 aut.); Atmospheric Chemistry Division, National Center for Atmospheric Research/Boulder, Colorado/Etats-Unis (4 aut.); Group of Chemistry and Physics of the Atmosphere, University of the Azores/Terra Cha/Portugal (5 aut., 6 aut.)</AF>
<DT>Publication en série; Niveau analytique</DT>
<SO>Journal of geophysical research; ISSN 0148-0227; Etats-Unis; Da. 2006; Vol. 111; No. D23; D23S60.1-D23S60.17; Bibl. 1 p.3/4</SO>
<LA>Anglais</LA>
<EA>[1] Extensive wildfires burned in northern North America during summer 2004, releasing large amounts of trace gases and aerosols into the atmosphere. Emissions from these wildfires frequently impacted the PICO-NARE station, a mountaintop site situated 6-15 days downwind from the fires in the Azores Islands. To assess the impacts of the boreal wildfire emissions on the levels of aerosol black carbon (BC), nitrogen oxides and O
<sub>3</sub>
downwind from North America, we analyzed measurements of CO, BC, total reactive nitrogen oxides (NOy), NO
<sub>x</sub>
(NO + NO
<sub>2</sub>
) and O
<sub>3</sub>
made from June to September 2004 in combination with MOZART chemical transport model simulations. Long-range transport of boreal wildfire emissions resulted in large enhancements of CO, BC, NO
<sub>y</sub>
and NO
<sub>x</sub>
, with levels up to 250 ppbv, 665 ng m
<sup>-3</sup>
, 1100 pptv and 135 pptv, respectively. Enhancement ratios relative to CO were variable in the plumes sampled, most likely because of variations in wildfire emissions and removal processes during transport. Analyses of ABC/ACO, ΔNO
<sub>y</sub>
/ΔCO and ΔNO
<sub>x</sub>
/ΔCO ratios indicate that NO
<sub>y</sub>
and BC were on average efficiently exported in these plumes and suggest that decomposition of PAN to NO
<sub>x</sub>
was a significant source of NO
<sub>x</sub>
. High levels of NO
<sub>x</sub>
suggest continuing formation of O
<sub>3</sub>
in these well-aged plumes. O
<sub>3</sub>
levels were also significantly enhanced in the plumes, reaching up to 75 ppbv. Analysis of ΔO
<sub>3</sub>
/ΔCO ratios showed distinct behaviors of O
<sub>3</sub>
in the plumes, which varied from significant to lower O
<sub>3</sub>
production. We identify several potential reasons for the complex effects of boreal wildfire emissions on O
<sub>3</sub>
and conclude that this behavior needs to be explored further in the future. These observations demonstrate that boreal wildfire emissions significantly contributed to the NO
<sub>x</sub>
and O
<sub>3</sub>
budgets in the central North Atlantic lower free troposphere during summer 2004 and imply large-scale impacts on direct radiative forcing of the atmosphere and on tropospheric NO
<sub>x</sub>
and O
<sub>3</sub>
.</EA>
<CC>220; 001E; 001E01</CC>
<FD>Oxyde azote; Azote oxyde; Suie; Ozone; Troposphère; Boréal; Amérique du Nord; Eté; Composé trace; Aérosol; Atmosphère; Incendie; Ile; Transport grande distance; Modèle; Simulation; Panache; Exportation; Transfert radiatif; Forçage; Océan Atlantique Nord; Açores</FD>
<FG>Océan Atlantique; Iles Océan Atlantique</FG>
<ED>nitrogen oxide; Nitrogen oxide; Soot; ozone; troposphere; Boreal; North America; Summer; Trace compound; aerosols; atmosphere; fires; islands; Long-range transport; models; simulation; plumes; export; Radiative transfer; Forcing; North Atlantic; Azores</ED>
<EG>Atlantic Ocean; Atlantic Ocean Islands</EG>
<SD>Nitrógeno óxido; Hollín; Ozono; Boreal; America del norte; Verano; Compuesto huella; Aerosol; Atmósfera; Isla; Modelo; Simulación; Penacho; Exportación; Transferencia radiativa; Forzamiento; Océano Atlántico Norte; Azores</SD>
<LO>INIST-3144.354000145302170450</LO>
<ID>07-0066720</ID>
</server>
</inist>
</record>

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