Atmospheric Chemistry and Physics (Apr 2019)

The distribution of sea-salt aerosol in the global troposphere

  • D. M. Murphy,
  • K. D. Froyd,
  • K. D. Froyd,
  • H. Bian,
  • H. Bian,
  • C. A. Brock,
  • J. E. Dibb,
  • J. P. DiGangi,
  • G. Diskin,
  • M. Dollner,
  • A. Kupc,
  • A. Kupc,
  • A. Kupc,
  • E. M. Scheuer,
  • G. P. Schill,
  • G. P. Schill,
  • B. Weinzierl,
  • B. Weinzierl,
  • C. J. Williamson,
  • C. J. Williamson,
  • P. Yu,
  • P. Yu,
  • P. Yu

DOI
https://doi.org/10.5194/acp-19-4093-2019
Journal volume & issue
Vol. 19
pp. 4093 – 4104

Abstract

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We present the first data on the concentration of sea-salt aerosol throughout most of the depth of the troposphere and over a wide range of latitudes, which were obtained during the Atmospheric Tomography (ATom) mission. Sea-salt concentrations in the upper troposphere are very small, usually less than 10 ng per standard m3 (about 10 parts per trillion by mass) and often less than 1 ng m−3. This puts stringent limits on the contribution of sea-salt aerosol to halogen and nitric acid chemistry in the upper troposphere. Within broad regions the concentration of sea-salt aerosol is roughly proportional to water vapor, supporting a dominant role for wet scavenging in removing sea-salt aerosol from the atmosphere. Concentrations of sea-salt aerosol in the winter upper troposphere are not as low as in the summer and the tropics. This is mostly a consequence of less wet scavenging in the drier, colder winter atmosphere. There is also a source of sea-salt aerosol over pack ice that is distinct from that over open water. With a well-studied and widely distributed source, sea-salt aerosol provides an excellent test of wet scavenging and vertical transport of aerosols in chemical transport models.