A tropospheric ozone maximum over the Middle East

被引:111
作者
Li, QB
Jacob, DJ
Logan, JA
Bey, I
Yantosca, RM
Liu, HY
Martin, RV
Fiore, AM
Field, BD
Duncan, BN
Thouret, V
机构
[1] Harvard Univ, Dept Earth & Planetary Sci, Cambridge, MA 02138 USA
[2] Harvard Univ, Div Engn & Appl Sci, Cambridge, MA 02138 USA
[3] CNRS, Lab Aerol, UMR 5560, Toulouse, France
关键词
D O I
10.1029/2001GL013134
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
The GEOS-CHEM global 3-D model of tropospheric chemistry predicts a summertime O-3 maximum over the Middle East, with mean mixing ratios in the middle and upper troposphere in excess of 80 ppbv. This model feature is consistent with the few observations from commercial aircraft in the region. Its origin in the model reflects a complex interplay of dynamical and chemical factors, and of anthropogenic and natural influences. The anticyclonic circulation in the middle and upper troposphere over the Middle East funnels northern midlatitude pollution transported in the westerly subtropical jet as well as lightning outflow from the Indian monsoon and pollution from eastern Asia transported in an easterly tropical jet. Large-scale subsidence over the region takes place with continued net production Of O-3 and little mid-level outflow. Transport from the stratosphere does not contribute significantly to the 03 maximum. Sensitivity simulations with anthropogenic or lightning emissions shut off indicate decreases of 20-30% and 10-15% respectively in the tropospheric O-3 column over the Middle East. More observations in this region are needed to confirm the presence of the O-3 maximum.
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收藏
页码:3235 / 3238
页数:4
相关论文
共 26 条
[1]   Global gridded inventories of anthropogenic emissions of sulfur and nitrogen [J].
Benkovitz, CM ;
Scholtz, MT ;
Pacyna, J ;
Tarrason, L ;
Dignon, J ;
Voldner, EC ;
Spiro, PA ;
Logan, JA ;
Graedel, TE .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D22) :29239-29253
[2]  
BEY I, 2001, IN PRESS J GEOPHYS R
[3]   Large-scale nitrogen oxide plumes in the tropopause region and implications for ozone [J].
Brunner, D ;
Staehelin, J ;
Jeker, D .
SCIENCE, 1998, 282 (5392) :1305-1309
[4]  
Christian HJ, 1998, Q J ROY METEOR SOC, V124, P1771, DOI 10.1002/qj.49712454919
[5]  
DAYAN U, 1986, J CLIM APPL METEOROL, V25, P591, DOI 10.1175/1520-0450(1986)025<0591:COBTFI>2.0.CO
[6]  
2
[7]   MOZART, a global chemical transport model for ozone and related chemical tracers 2. Model results and evaluation [J].
Hauglustaine, DA ;
Brasseur, GP ;
Walters, S ;
Rasch, PJ ;
Muller, JF ;
Emmons, LK ;
Carroll, CA .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D21) :28291-28335
[8]  
HOROWITZ LW, 2001, EOS T AGU, V82, pS39
[9]   Chemistry of HOx radicals in the upper troposphere [J].
Jaeglé, L ;
Jacob, DJ ;
Brune, WH ;
Wennberg, PO .
ATMOSPHERIC ENVIRONMENT, 2001, 35 (03) :469-489
[10]   Model calculations of present and future levels of ozone and ozone precursors with a global and a regional model [J].
Jonson, JE ;
Sundet, JK ;
Tarrasón, L .
ATMOSPHERIC ENVIRONMENT, 2001, 35 (03) :525-537