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  • Environment Pollution; Earth Resources and Remote Sensing  (1)
  • water vapor profiles  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 30 (1998), S. 11-23 
    ISSN: 1573-0662
    Keywords: Polar stratospheric clouds ; stratospheric aerosol ; water vapor profiles ; decay of Pinatubo aerosol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Vertical profiles of aerosol were measured in February 1993, and January - March 1995 using balloon-borne particle counters released from Kiruna, Sweden. Condensation nuclei (CN) and aerosol with radii ≥ 0.15 - 10.0 µm were measured in 8-12 size classes. The three flights in 1993 were within the polar vortex. Temperatures were below polar stratospheric cloud (PSC) threshold temperatures on one flight and a thin PSC was observed. The volcanic aerosol in the 1993 vortex was similar to that in 1992. In 1993, surface areas were 10 - 20 µm2 cm-3 and volumes 1 - 3 µm3 cm-3. In 1995 three of five flights were within the polar vortex. The volcanic aerosol had decreased to 3 - 7 µm2 cm-3 and 0.1 - 0.4 µm3 cm-3. The top of the volcanic aerosol layer in both years was near 500 K potential temperature (~20 km). A thick nitric acid and water PSC was observed in January 1995. In the thickest region of this PSC nearly all CN were observed to be activated, and surface areas of 5 - 10 µm2 cm-3 were calculated. The volumes observed in this PSC were closer to what would be expected for particles composed of nitric acid trihydrate than for ternary solution droplets. In 1993 the opposite was observed, the volumes in the thin PSC were closer to what would be expected for ternary solution droplets.
    Type of Medium: Electronic Resource
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  • 2
    Publication Date: 2019-08-26
    Description: 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 (approximately 20 - 40 ppbv) O3, occurs in approximately 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.
    Keywords: Environment Pollution; Earth Resources and Remote Sensing
    Type: GSFC-E-DAA-TN34907 , Journal of Geophysical Research: Atmospheres (ISSN 2169-897X) (e-ISSN 2169-8996); 122; 2; 1261-1280
    Format: application/pdf
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