Stratospheric air intrusions promote global-scale new particle formation

Author:

Zhang Jiaoshi1ORCID,Gong Xianda1ORCID,Crosbie Ewan23ORCID,Diskin Glenn2ORCID,Froyd Karl45ORCID,Hall Samuel6ORCID,Kupc Agnieszka457ORCID,Moore Richard2ORCID,Peischl Jeff45ORCID,Rollins Andrew5ORCID,Schwarz Joshua5ORCID,Shook Michael2ORCID,Thompson Chelsea45ORCID,Ullmann Kirk6ORCID,Williamson Christina4589ORCID,Wisthaler Armin1011ORCID,Xu Lu1ORCID,Ziemba Luke2ORCID,Brock Charles A.5ORCID,Wang Jian1ORCID

Affiliation:

1. Center for Aerosol Science and Engineering, Department of Energy, Environmental and Chemical Engineering, Washington University in St. Louis, St. Louis, MO, USA.

2. NASA Langley Research Center, Hampton, VA, USA.

3. Science Systems and Applications, Inc., Hampton, VA, USA.

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

5. Chemical Sciences Laboratory, National Oceanic and Atmospheric Administration, Boulder, CO, USA.

6. Atmospheric Chemistry Observations and Modeling Laboratory, National Center for Atmospheric Research, Boulder, CO, USA.

7. Faculty of Physics, Aerosol Physics and Environmental Physics, University of Vienna, Vienna, Austria.

8. Climate Research Programme, Finnish Meteorological Institute, Helsinki, Finland.

9. Institute for Atmospheric and Earth System Research/Physics, Faculty of Science, University of Helsinki, Helsinki, Finland.

10. Institute for Ion Physics and Applied Physics, University of Innsbruck, Innsbruck, Austria.

11. Department of Chemistry, University of Oslo, Oslo, Norway.

Abstract

New particle formation in the free troposphere is a major source of cloud condensation nuclei globally. The prevailing view is that in the free troposphere, new particles are formed predominantly in convective cloud outflows. We present another mechanism using global observations. We find that during stratospheric air intrusion events, the mixing of descending ozone-rich stratospheric air with more moist free tropospheric background results in elevated hydroxyl radical (OH) concentrations. Such mixing is most prevalent near the tropopause where the sulfur dioxide (SO 2 ) mixing ratios are high. The combination of elevated SO 2 and OH levels leads to enhanced sulfuric acid concentrations, promoting particle formation. Such new particle formation occurs frequently and over large geographic regions, representing an important particle source in the midlatitude free troposphere.

Publisher

American Association for the Advancement of Science (AAAS)

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