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Tropospheric ozonesonde profiles at long-term U.S. monitoring sites: 2. Links between Trinidad Head CA profile clusters and inland surface ozone measurements

机译:美国长期监测站的对流层臭氧探空仪剖面图:2.特立尼达海德加利福尼亚剖面群与内陆表面臭氧测量之间的联系

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摘要

Much attention has been focused on the transport of ozone (O3) to the Western U.S., particularly given the latest revision of the National Ambient Air Quality Standard (NAAQS) to 70 parts per billion by volume (ppbv) of O3. This makes defining a “background” O3 amount essential so that the effects of stratosphere-to-troposphere exchange and pollution transport to this region can be quantified. To evaluate free-tropospheric and surface O3 in the Western U.S., we use self-organizing maps to cluster 18 years of ozonesonde profiles (940 samples) from Trinidad Head, CA. Two of nine O3 mixing ratio profile clusters exhibit thin laminae of high O3 above Trinidad Head. A third, consisting of background (~20 – 40 ppbv) O3, occurs in ~10% of profiles. The high O3 layers are located between 1 and 4 km amsl, and reside above a subsidence inversion associated with a northern location of the semi-permanent Pacific subtropical high. Several ancillary data sets are examined to identify the high O3 sources (reanalyses, trajectories, remotely-sensed carbon monoxide), but distinguishing chemical and stratospheric influences of the elevated O3 is difficult. There is marked and long-lasting impact of the elevated tropospheric O3 on high-altitude surface O3 monitors at Lassen Volcanic and Yosemite National Parks, and Truckee, CA. Days corresponding to the high O3 clusters exhibit hourly surface O3 anomalies of +5 – 10 ppbv compared to a climatology; the anomalies can last up to four days. The profile and surface O3 links demonstrate the importance of regular ozonesonde profiling at Trinidad Head.
机译:臭氧(O3)向美国西部的运输已经引起了很多关注,特别是考虑到国家环境空气质量标准(NAAQS)的最新修订为O3的体积百分含量(ppbv)70。这使得确定“本底” O3量至关重要,这样就可以量化平流层到对流层交换和污染向该区域的迁移的影响。为了评估美国西部的对流层和地面O3,我们使用自组织图对来自加利福尼亚特立尼达黑德的18年臭氧探空仪剖面(940个样本)进行聚类。九个O3混合比率剖面簇中的两个在特立尼达海德上方显示出薄薄的高O3薄片。第三个由背景(约20至40 ppbv)O3组成,约占分布的10%。较高的O3层位于1-4 km amsl之间,并位于与半永久性太平洋副热带高压的北部位置相关的沉降反演之上。检查了几个辅助数据集以识别高O3来源(重新分析,轨迹,遥感一氧化碳),但是很难区分升高的O3的化学和平流层影响。对流层O3升高对拉森火山和优胜美地国家公园以及加利福尼亚州特拉基的高海拔地面O3监测器产生了明显而持久的影响。与气候相比,与高O3簇相对应的天数小时表面O3异常为+5 ppbv。异常可能持续长达四天。剖面和表面O3链接显示了特立尼达海德定期进行臭氧探空仪剖析的重要性。

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