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 : 000144Significant 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. BarataSource :
- Journal of geophysical research [ 0148-0227 ] ; 2006.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
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.
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Pour connaître la documentation sur le format Inist Standard.
pA |
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Format Inist (serveur)
NO : | PASCAL 07-0066720 INIST |
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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 |
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Pascal:07-0066720Le document en format XML
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Significant enhancements of nitrogen oxides, black carbon, and ozone in the North Atlantic lower free troposphere resulting from North American boreal wildfires</title>
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<series><title level="j" type="main">Journal of geophysical research</title>
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<term>Long-range transport</term>
<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>
<term>simulation</term>
<term>troposphere</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Oxyde azote</term>
<term>Azote oxyde</term>
<term>Suie</term>
<term>Ozone</term>
<term>Troposphère</term>
<term>Boréal</term>
<term>Amérique du Nord</term>
<term>Eté</term>
<term>Composé trace</term>
<term>Aérosol</term>
<term>Atmosphère</term>
<term>Incendie</term>
<term>Ile</term>
<term>Transport grande distance</term>
<term>Modèle</term>
<term>Simulation</term>
<term>Panache</term>
<term>Exportation</term>
<term>Transfert radiatif</term>
<term>Forçage</term>
<term>Océan Atlantique Nord</term>
<term>Açores</term>
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<front><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>
</front>
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<fA11 i1="01" i2="1"><s1>VAL MARTIN (M.)</s1>
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<fA14 i1="02"><s1>Atmospheric Chemistry Division, National Center for Atmospheric Research</s1>
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<fA14 i1="03"><s1>Group of Chemistry and Physics of the Atmosphere, University of the Azores</s1>
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<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>
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<fC02 i1="01" i2="2"><s0>220</s0>
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<s5>05</s5>
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<fC03 i1="06" i2="2" l="FRE"><s0>Boréal</s0>
<s5>06</s5>
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<fC03 i1="06" i2="2" l="ENG"><s0>Boreal</s0>
<s5>06</s5>
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<fC03 i1="06" i2="2" l="SPA"><s0>Boreal</s0>
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<fC03 i1="07" i2="2" l="ENG"><s0>North America</s0>
<s5>07</s5>
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<s5>07</s5>
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<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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