The impact of aircraft nitrogen oxide emissions on tropospheric ozone studied with a 3D Lagrangian model including fully diurnal chemistry

被引:41
作者
Stevenson, DS
Collins, WJ
Johnson, CE
Derwent, RG
机构
[1] Atmospheric Processes Research, Meteorological Office, Bracknell, RG12 2SZ, London Rd.
[2] Hadley Ctr. Climate Prediction Res., Meteorological Office, Bracknell, RG12 2SY, London Rd.
关键词
3D model; tropospheric chemistry; NOx; aircraft emissions; ozone; climate change; TRANSPORT; CLIMATE; EXHAUST;
D O I
10.1016/S1352-2310(96)00333-0
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A three-dimensional Lagrangian tropospheric chemistry-transport model is used to investigate the impact of aircraft NOx emissions upon the concentrations of ozone and hydroxyl radicals. The model has a five minute chemistry time-step, and a three-hour advection time step, and hence resolves diurnal variations in chemistry,The model contains a representation of tropospheric inorganic chemistry, as well as that of methane and nine emitted hydrocarbons. Aircraft NOx emissions were found to contribute up to 20-60% towards background upper troposphere NOx levels, and to be responsible for up to 5-10% of upper tropospheric O-3, with a maximum contribution in April. The magnitude of the peak ozone change in July is 13 ppb and 8.5 ppb in January, and its location shifts with incident solar radiation. Calculated globally averaged radiative forcing exerted by the extra ozone is 0.05 W m(-2), mainly concentrated in the Northern hemisphere. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1837 / 1850
页数:14
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