Stauffer Ryan M, Thompson Anne M, Oltmans Samuel J, Johnson Bryan J
Earth System Science Interdisciplinary Center (ESSIC), University of Maryland - College Park, College Park, Maryland, USA.
Department of Meteorology, The Pennsylvania State University, University Park, Pennsylvania, USA.
J Geophys Res Atmos. 2017 Jan 27;122(2):1261-1280. doi: 10.1002/2016JD025254. Epub 2016 Dec 6.
Much attention has been focused on the transport of ozone (O) 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 O. This makes defining a "background" O 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 O 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 O mixing ratio profile clusters exhibit thin laminae of high O above Trinidad Head. A third, consisting of background (~20 - 40 ppbv) O, occurs in ~10% of profiles. The high O 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 O sources (reanalyses, trajectories, remotely-sensed carbon monoxide), but distinguishing chemical and stratospheric influences of the elevated O is difficult. There is marked and long-lasting impact of the elevated tropospheric O on high-altitude surface O monitors at Lassen Volcanic and Yosemite National Parks, and Truckee, CA. Days corresponding to the high O clusters exhibit hourly surface O anomalies of +5 - 10 ppbv compared to a climatology; the anomalies can last up to four days. The profile and surface O links demonstrate the importance of regular ozonesonde profiling at Trinidad Head.
人们一直非常关注臭氧(O₃)向美国西部的传输,特别是考虑到国家环境空气质量标准(NAAQS)最新修订为体积分数70 ppbv的O₃。这使得确定“背景”O₃量至关重要,以便能够量化平流层到对流层的交换以及向该地区的污染传输的影响。为了评估美国西部对流层和平流层的O₃,我们使用自组织映射对加利福尼亚州特立尼达角18年的臭氧探空仪剖面(940个样本)进行聚类。九个O₃混合比剖面聚类中的两个显示特立尼达角上方有高O₃的薄层。第三个聚类由背景(约20 - 40 ppbv)O₃组成,约占剖面的10%。高O₃层位于平均海平面以上1至4公里处,位于与半永久性太平洋副热带高压北部位置相关的下沉逆温层之上。我们检查了几个辅助数据集以确定高O₃的来源(再分析、轨迹、遥感一氧化碳),但区分升高的O₃的化学和平流层影响很困难。对流层O₃升高对拉森火山国家公园、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监测器有显著且持久的影响。与气候学相比,对应高O₃聚类的日子每小时地面O₃异常为 +5 - 10 ppbv;这些异常可持续长达四天。剖面和地面O₃的联系表明在特立尼达角定期进行臭氧探空仪剖面测量的重要性。