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首页> 外文期刊>Journal of Geophysical Research, D. Atmospheres: JGR >Diagnosing the stratosphere-to-troposphere flux of ozone in a chemistry transport model
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Diagnosing the stratosphere-to-troposphere flux of ozone in a chemistry transport model

机译:诊断的stratosphere-to-troposphere通量臭氧在化学传输模式

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Events involving stratosphere-troposphere exchange (STE) of ozone, such as tropopause folds and westerly ducts, are readily identified in observations and models, but a quantitative flux specifying where and when stratospheric ozone is mixed into the troposphere is not readily discerned from either. This work presents a new diagnostic based on determining when stratospheric air is mixed and diluted down to tropospheric abundances (<100 ppb) and hence effectively participates in tropospheric chemistry. The method is applied to two years of high-resolution, global meteorological fields (1.9 degrees, 40 levels) from the ECMWF forecast model derived by U. Oslo for chemistry transport modeling and used in TRACE-P studies. The UCI CTM is run here with linearized stratospheric ozone chemistry (Linoz) and a parameterized tropospheric sink. In terms of events, the CTM accurately follows a March 2001 westerly duct stratospheric intrusion into the tropical eastern Pacific as observed by TOMS and calculates a 48-hour burst of STE O3 flux for that region. The influx associated with the event (0.3 Tg) is much less than the anomalous amount seen as an isolated island in column ozone (1.7 Tg). A climatology of monthly mean STE fluxes is similar for both years (January to December 1997 and May 2000 to April 2001), but the warm phase of ENSO December 1997 is distinctly different from the cold phase of ENSO month December 2000. Global ozone fluxes are about 515 Tg (year 1997) and 550 Tg (year 2000/2001) with an equal amount into each hemisphere, and larger springtime fluxes for both hemispheres. In terms of geographical distribution, Northern Hemisphere regions of high ozone flux follow the jet streams over the oceans in the winter and over the continents in the summer, in agreement with many previous studies. In contrast, we find the largest STE flux is located in the subtropics during late spring, particularly over the Tibetan Plateau in May. This hot spot of STE is not a numerical artifact, it occurs in both meteorological years, and it appears to be caused by the rapid erosion of the tropopause. Ozone fluxes in the Southern Hemisphere have less variability (either temporal or spatial), and they occur mainly in the subtropical region (25°S–35°S) regardless of season. The poles, throughout the year, show minimal STE O3 flux.
机译:事件涉及stratosphere-troposphere交换(STE)臭氧,比如对流层顶折叠西风导管,很容易识别观察和模型,但定量通量指定当平流层臭氧在哪里混合到对流层并不容易从。基于时确定诊断极高的空气混合,稀释对流层丰度(< 100磅),因此有效地参与对流层化学。高分辨率、全球气象领域(1.9度,40的水平)的ECMWF预报模型导出了奥斯陆化学运输建模和TRACE-P研究中使用。与线性化平流层臭氧运行吗化学(Linoz)和参数化对流层下沉。准确地遵循2001年3月西风导管平流层侵入热带东部太平洋汤姆斯观察到和计算48小时的STE O3通量的地区。流入相关事件(0.3 Tg)不到视为异常数量孤岛臭氧列(1.7 Tg)。气候学月度STE通量是相似的两年来(1997年1月至12月和5月2000年到2001年4月),但ENSO的温暖的阶段1997年12月是截然不同的2000年12月ENSO月冷阶段。臭氧流量约为515 Tg(1997年)和550年Tg(2000/2001)等量每个半球,春天大通量两个半球。分布,北半球地区高海洋上空的臭氧流量按照急流在冬天的大洲夏天,许多之前的研究结果相一致。相比之下,我们发现最大的STE通量在春末位于亚热带,尤其是在青藏高原。这个热点的STE不是一个数值的工件,它发生在气象年,似乎是由快速侵蚀引起的对流层顶。半球可变性(时间更少或空间),他们主要在发生亚热带地区(25°打进35°S)不管的季节。最小的STE O3通量。

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