Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008

We quantify source contributions to springtime (April 2008) surface black carbon (BC) in the Arctic by interpreting surface observations of BC at five receptor sites (Denali, Barrow, Alert, Zeppelin, and Summit) using a global chemical transport model (GEOS-Chem) and its adjoint. Contributions to...

Full description

Bibliographic Details
Main Authors: L. Qi, Q. Li, D. K. Henze, H.-L. Tseng, C. He
Format: Article
Language:English
Published: Copernicus Publications 2017-08-01
Series:Atmospheric Chemistry and Physics
Online Access:https://www.atmos-chem-phys.net/17/9697/2017/acp-17-9697-2017.pdf
id doaj-0ab50dc7671e4221a2614da063086cda
record_format Article
spelling doaj-0ab50dc7671e4221a2614da063086cda2020-11-25T00:35:01ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242017-08-01179697971610.5194/acp-17-9697-2017Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008L. Qi0L. Qi1Q. Li2Q. Li3D. K. Henze4H.-L. Tseng5H.-L. Tseng6C. He7C. He8Department of Atmospheric and Oceanic Sciences, University of California, Los Angeles, CA, USAJoint Institute for Regional Earth System Science and Engineering, University of California, Los Angeles, CA, USADepartment of Atmospheric and Oceanic Sciences, University of California, Los Angeles, CA, USAJoint Institute for Regional Earth System Science and Engineering, University of California, Los Angeles, CA, USADepartment of Mechanical Engineering, University of Colorado, Boulder, CO, USADepartment of Atmospheric and Oceanic Sciences, University of California, Los Angeles, CA, USAJoint Institute for Regional Earth System Science and Engineering, University of California, Los Angeles, CA, USADepartment of Atmospheric and Oceanic Sciences, University of California, Los Angeles, CA, USAJoint Institute for Regional Earth System Science and Engineering, University of California, Los Angeles, CA, USAWe quantify source contributions to springtime (April 2008) surface black carbon (BC) in the Arctic by interpreting surface observations of BC at five receptor sites (Denali, Barrow, Alert, Zeppelin, and Summit) using a global chemical transport model (GEOS-Chem) and its adjoint. Contributions to BC at Barrow, Alert, and Zeppelin are dominated by Asian anthropogenic sources (40–43 %) before 18 April and by Siberian open biomass burning emissions (29–41 %) afterward. In contrast, Summit, a mostly free tropospheric site, has predominantly an Asian anthropogenic source contribution (24–68 %, with an average of 45 %). We compute the adjoint sensitivity of BC concentrations at the five sites during a pollution episode (20–25 April) to global emissions from 1 March to 25 April. The associated contributions are the combined results of these sensitivities and BC emissions. Local and regional anthropogenic sources in Alaska are the largest anthropogenic sources of BC at Denali (63 % of total anthropogenic contributions), and natural gas flaring emissions in the western extreme north of Russia (WENR) are the largest anthropogenic sources of BC at Zeppelin (26 %) and Alert (13 %). We find that long-range transport of emissions from Beijing–Tianjin–Hebei (also known as Jing–Jin–Ji), the biggest urbanized region in northern China, contribute significantly (∼ 10 %)</span> to surface BC across the Arctic. On average, it takes ∼ 12 days for Asian anthropogenic emissions and Siberian biomass burning emissions to reach the Arctic lower troposphere, supporting earlier studies. Natural gas flaring emissions from the WENR reach Zeppelin in about a week. We find that episodic transport events dominate BC at Denali (87 %), a site outside the Arctic front, which is a strong transport barrier. The relative contribution of these events to surface BC within the polar dome is much smaller (∼ 50 % at Barrow and Zeppelin and ∼ 10 % at Alert). The large contributions from Asian anthropogenic sources are predominately in the form of <q>chronic</q> pollution (∼ 40 % at Barrow, 65 % at Alert, and 57 % at Zeppelin) on about a 1-month timescale. As such, it is likely that previous studies using 5- or 10-day trajectory analyses strongly underestimated the contribution from Asia to surface BC in the Arctic.https://www.atmos-chem-phys.net/17/9697/2017/acp-17-9697-2017.pdf
collection DOAJ
language English
format Article
sources DOAJ
author L. Qi
L. Qi
Q. Li
Q. Li
D. K. Henze
H.-L. Tseng
H.-L. Tseng
C. He
C. He
spellingShingle L. Qi
L. Qi
Q. Li
Q. Li
D. K. Henze
H.-L. Tseng
H.-L. Tseng
C. He
C. He
Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008
Atmospheric Chemistry and Physics
author_facet L. Qi
L. Qi
Q. Li
Q. Li
D. K. Henze
H.-L. Tseng
H.-L. Tseng
C. He
C. He
author_sort L. Qi
title Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008
title_short Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008
title_full Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008
title_fullStr Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008
title_full_unstemmed Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008
title_sort sources of springtime surface black carbon in the arctic: an adjoint analysis for april 2008
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2017-08-01
description We quantify source contributions to springtime (April 2008) surface black carbon (BC) in the Arctic by interpreting surface observations of BC at five receptor sites (Denali, Barrow, Alert, Zeppelin, and Summit) using a global chemical transport model (GEOS-Chem) and its adjoint. Contributions to BC at Barrow, Alert, and Zeppelin are dominated by Asian anthropogenic sources (40–43 %) before 18 April and by Siberian open biomass burning emissions (29–41 %) afterward. In contrast, Summit, a mostly free tropospheric site, has predominantly an Asian anthropogenic source contribution (24–68 %, with an average of 45 %). We compute the adjoint sensitivity of BC concentrations at the five sites during a pollution episode (20–25 April) to global emissions from 1 March to 25 April. The associated contributions are the combined results of these sensitivities and BC emissions. Local and regional anthropogenic sources in Alaska are the largest anthropogenic sources of BC at Denali (63 % of total anthropogenic contributions), and natural gas flaring emissions in the western extreme north of Russia (WENR) are the largest anthropogenic sources of BC at Zeppelin (26 %) and Alert (13 %). We find that long-range transport of emissions from Beijing–Tianjin–Hebei (also known as Jing–Jin–Ji), the biggest urbanized region in northern China, contribute significantly (∼ 10 %)</span> to surface BC across the Arctic. On average, it takes ∼ 12 days for Asian anthropogenic emissions and Siberian biomass burning emissions to reach the Arctic lower troposphere, supporting earlier studies. Natural gas flaring emissions from the WENR reach Zeppelin in about a week. We find that episodic transport events dominate BC at Denali (87 %), a site outside the Arctic front, which is a strong transport barrier. The relative contribution of these events to surface BC within the polar dome is much smaller (∼ 50 % at Barrow and Zeppelin and ∼ 10 % at Alert). The large contributions from Asian anthropogenic sources are predominately in the form of <q>chronic</q> pollution (∼ 40 % at Barrow, 65 % at Alert, and 57 % at Zeppelin) on about a 1-month timescale. As such, it is likely that previous studies using 5- or 10-day trajectory analyses strongly underestimated the contribution from Asia to surface BC in the Arctic.
url https://www.atmos-chem-phys.net/17/9697/2017/acp-17-9697-2017.pdf
work_keys_str_mv AT lqi sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
AT lqi sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
AT qli sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
AT qli sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
AT dkhenze sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
AT hltseng sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
AT hltseng sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
AT che sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
AT che sourcesofspringtimesurfaceblackcarboninthearcticanadjointanalysisforapril2008
_version_ 1725310831645687808