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Stratospheric impact on tropospheric ozone variability and trends: 1990–2009

机译:对流层臭氧变异性和趋势的平流层影响:1990-2009

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摘要

The influence of stratospheric ozone on the interannual variability and trends in tropospheric ozone is evaluated between 30 and 90° N from 1990–2009 using ozone measurements and a global chemical transport model, the Community Atmospheric Model with chemistry (CAM-chem). Long-term measurements from ozonesondes, at 150 and 500 hPa, and the Measurements of OZone and water vapour by in-service Airbus aircraft programme (MOZAIC), at 500 hPa, are analyzed over Japan, Canada, the Eastern US and Northern and Central Europe. The measurements generally emphasize northern latitudes, although the simulation suggests that measurements over the Canadian, Northern and Central European regions are representative of the large-scale interannual ozone variability from 30 to 90° N at 500 hPa. CAM-chem is run with input meteorology from the National Center for Environmental Prediction; a tagging methodology is used to identify the stratospheric contribution to tropospheric ozone concentrations. A variant of the synthetic ozone tracer (synoz) is used to represent stratospheric ozone. Both the model and measurements indicate that on large spatial scales stratospheric interannual ozone variability drives significant tropospheric variability at 500 hPa and the surface. In particular, the simulation and the measurements suggest large stratospheric influence at the surface sites of Mace Head (Ireland) and Jungfraujoch (Switzerland) as well as many 500 hPa measurement locations. Both the measurements and simulation suggest the stratosphere has contributed to tropospheric ozone trends. In many locations between 30–90° N 500 hPa ozone significantly increased from 1990–2000, but has leveled off since (from 2000–2009). The simulated global ozone budget suggests global stratosphere-troposphere exchange increased in 1998–1999 in association with a global ozone anomaly. Discrepancies between the simulated and measured ozone budget include a large underestimation of measured ozone variability and discrepancies in long-term stratospheric ozone trends. This suggests the need for more sophisticated simulations including better representations of stratospheric chemistry and circulation.
机译:利用臭氧测量和全球化学传输模型,与化学(CAM-Chem)的社区大气模型,评估了分流层臭氧对对流层臭氧的续变性和趋势的影响。从日本,加拿大,东美国东部和北部和中央,从150和500 HPA,150和500 HPA,150和500 HPA的臭氧和水蒸气测量臭氧和水蒸气的测量值欧洲。测量通常会强调北纬,尽管模拟表明,在加拿大,北部和中央欧洲地区的测量表明,在500hPa下的30至90°N的大规模持续臭氧可变性。 Cam-Chem与国家环境预测中心的输入气象运行;标记方法用于识别对流层臭氧浓度的平流层贡献。合成臭氧示踪剂(Synoz)的变型用于表示平坦散臭型臭氧。模型和测量都表明,在大型空间尺度上,平流层续臭氧可变性在500 HPA和表面下驱动显着的对流层变异性。特别地,模拟和测量表明了MACE Head(爱尔兰)和Jungfraujoch(瑞士)以及许多500 HPA测量位置的大型平流层影响。测量和仿真都表明平流层有助于对流层臭氧趋势。在30-90°N 500 HPA臭氧之间的许多位置,从1990 - 2000年显着增加,但自以来(从2000-2009)以来已经升级。模拟全球臭氧预算表明​​,全球平流层 - 对流层交流与全球臭氧异常相关联的1998-1999。模拟和测量的臭氧预算之间的差异包括大量低估测量的臭氧变异性和长期平流层臭氧趋势的差异。这表明需要更复杂的模拟,包括平流层化学和循环的更好表示。

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