Quantifying Stratospheric Ozone in the Upper Troposphere with in Situ Measurements of HCl

Author:

Marcy T. P.12345,Fahey D. W.12345,Gao R. S.12345,Popp P. J.12345,Richard E. C.12345,Thompson T. L.12345,Rosenlof K. H.12345,Ray E. A.12345,Salawitch R. J.12345,Atherton C. S.12345,Bergmann D. J.12345,Ridley B. A.12345,Weinheimer A. J.12345,Loewenstein M.12345,Weinstock E. M.12345,Mahoney M. J.12345

Affiliation:

1. Aeronomy Laboratory, National Oceanic and Atmospheric Administration, Boulder, CO 80305, USA.

2. Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, CO 80309, USA.

3. Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA 91109, USA.

4. Atmospheric Science Division, Lawrence Livermore National Laboratory (LLNL), Livermore, CA 94550, USA.

5. National Center for Atmospheric Research, Boulder, CO 80307, USA.

Abstract

We have developed a chemical ionization mass spectrometry technique for precise in situ measurements of hydrochloric acid (HCl) from a high-altitude aircraft. In measurements at subtropical latitudes, minimum HCl values found in the upper troposphere (UT) were often near or below the detection limit of the measurements (0.005 parts per billion by volume), indicating that background HCl values are much lower than a global mean estimate. However, significant abundances of HCl were observed in many UT air parcels, as a result of stratosphere-to-troposphere transport events. We developed a method for diagnosing the amount of stratospheric ozone in these UT parcels using the compact linear correlation of HCl with ozone found throughout the lower stratosphere (LS). Expanded use of this method will lead to improved quantification of cross-tropopause transport events and validation of global chemical transport models.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference43 articles.

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4. F. C. Fehsenfeld, S. C. Liu, in Global Atmospheric Chemical Change, C. N. Hewitt, W. T. Sturges, Eds. (Elsevier, New York, 1993), pp. 169–231.

5. J. Geophys. Res. 2003 108

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