Bringing the ocean into the laboratory to probe the chemical complexity of sea spray aerosol

Kimberly A. Prather(Scripps Institution of Oceanography), Timothy H. Bertram(University of California San Diego), Vicki H. Grassian(University of Iowa), Grant B. Deane(Scripps Institution of Oceanography), M. Dale Stokes(Scripps Institution of Oceanography), Paul J. DeMott(Colorado State University), Lihini I. Aluwihare(Scripps Institution of Oceanography), Brian Palenik(Scripps Institution of Oceanography), Farooq Azam(Scripps Institution of Oceanography), John H. Seinfeld(California Institute of Technology), Ryan C. Moffet(University of the Pacific), Mario J. Molina(Scripps Institution of Oceanography), Christopher D. Cappa(University of California, Davis), Franz M. Geiger(Northwestern University), Greg Roberts(Scripps Institution of Oceanography), Lynn M. Russell(Scripps Institution of Oceanography), Andrew P. Ault(University of Iowa), Jonas Baltrušaitis(University of Iowa), Douglas B. Collins(University of California San Diego), C. Corrigan(Scripps Institution of Oceanography), Luis A. Cuadra‐Rodriguez(University of California San Diego), C. J. Ebben(Northwestern University), Sara D. Forestieri(University of California, Davis), Timothy L. Guasco(University of California San Diego), S. P. Hersey(California Institute of Technology), Michelle Kim(Scripps Institution of Oceanography), William Franklin Lambert(Scripps Institution of Oceanography), Robin L. Modini(Scripps Institution of Oceanography), Wilton Mui(California Institute of Technology), Byron E. Pedler(Scripps Institution of Oceanography), Matthew J. Ruppel(University of California San Diego), O. S. Ryder(University of California San Diego), Nathan G. Schoepp(University of California San Diego), Ryan C. Sullivan(Carnegie Mellon University), Defeng Zhao
Proceedings of the National Academy of Sciences
April 25, 2013
Cited by 660Open Access
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Abstract

The production, size, and chemical composition of sea spray aerosol (SSA) particles strongly depend on seawater chemistry, which is controlled by physical, chemical, and biological processes. Despite decades of studies in marine environments, a direct relationship has yet to be established between ocean biology and the physicochemical properties of SSA. The ability to establish such relationships is hindered by the fact that SSA measurements are typically dominated by overwhelming background aerosol concentrations even in remote marine environments. Herein, we describe a newly developed approach for reproducing the chemical complexity of SSA in a laboratory setting, comprising a unique ocean-atmosphere facility equipped with actual breaking waves. A mesocosm experiment was performed in natural seawater, using controlled phytoplankton and heterotrophic bacteria concentrations, which showed SSA size and chemical mixing state are acutely sensitive to the aerosol production mechanism, as well as to the type of biological species present. The largest reduction in the hygroscopicity of SSA occurred as heterotrophic bacteria concentrations increased, whereas phytoplankton and chlorophyll-a concentrations decreased, directly corresponding to a change in mixing state in the smallest (60-180 nm) size range. Using this newly developed approach to generate realistic SSA, systematic studies can now be performed to advance our fundamental understanding of the impact of ocean biology on SSA chemical mixing state, heterogeneous reactivity, and the resulting climate-relevant properties.


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