4.7 Article

A sea-state based source function for size- and composition-resolved marine aerosol production

Journal

ATMOSPHERIC CHEMISTRY AND PHYSICS
Volume 11, Issue 3, Pages 1203-1216

Publisher

COPERNICUS GESELLSCHAFT MBH
DOI: 10.5194/acp-11-1203-2011

Keywords

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Funding

  1. U.S. Department of Energy's Office of Science through the Office of Biological and Environmental Research [DE-FG02-07ER64442]
  2. Global Change Education Program Graduate Research Environmental Fellowship
  3. National Center for Computational Sciences at Oak Ridge National Laboratory (ONRL) [DE-AC05-00OR22725]
  4. National Science Foundation [ATM-0343146, ATM-0638741, ATM 0343199]

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A parameterization for the size- and composition-resolved production fluxes of nascent marine aerosol was developed from prior experimental observations and extrapolated to ambient conditions based on estimates of air entrainment by the breaking of wind-driven ocean waves. Production of particulate organic carbon (OCaer) was parameterized based on Langmuir equilibrium-type association of organic matter to bubble plumes in seawater and resulting aerosol as constrained by measurements of aerosol produced from productive and oligotrophic seawater. This novel approach is the first to parameterize size- and composition-resolved aerosol production based on explicit evaluation of wind-driven air entrainment/detrainment fluxes and chlorophyll-a as a proxy for surfactants in surface seawater. Production fluxes were simulated globally with an eight aerosol-size-bin version of the NCAR Community Atmosphere Model (CAM v3.5.07). Simulated production fluxes fell within the range of published estimates based on observationally constrained parameterizations. Because the parameterization does not consider contributions from spume drops, the simulated global mass flux (1.5 x 10(3) Tg y(-1)) is near the lower end of published estimates. The simulated production of aerosol number (1.4 x 10(6) m(-2) s(-1)) and OCaer (29 Tg C y(-1)) fall near the upper end of published estimates and suggest that primary marine aerosols may have greater influences on the physicochemical evolution of the troposphere, radiative transfer and climate, and associated feedbacks on the surface ocean than suggested by previous model studies.

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