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Volume 14, issue 10
Atmos. Chem. Phys., 14, 5057-5072, 2014
https://doi.org/10.5194/acp-14-5057-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.

Special issue: VAMOS Ocean-Cloud-Atmosphere-Land Study (VOCALS) (ACP/OS inter-journal...

Atmos. Chem. Phys., 14, 5057-5072, 2014
https://doi.org/10.5194/acp-14-5057-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 23 May 2014

Research article | 23 May 2014

Chemical composition and sources of coastal marine aerosol particles during the 2008 VOCALS-REx campaign

Y.-N. Lee1, S. Springston1, J. Jayne2, J. Wang1, J. Hubbe3, G. Senum1, L. Kleinman1, and P. H. Daum1 Y.-N. Lee et al.
  • 1Atmospheric Sciences Division, Brookhaven National Laboratory, Upton, NY 11973, USA
  • 2Aerodyne Research Inc., Bellerica, MA 01821, USA
  • 3Pacific Northwest National Laboratory, P.O. Box 999, K8-88, Richland, WA 99352, USA

Abstract. The chemical composition of aerosol particles (Dp ≤ 1.5 μm) was measured over the southeast Pacific Ocean during the VAMOS (Variability of the American Monsoon Systems) Ocean-Cloud-Atmosphere-Land Study Regional Experiment (VOCALS-Rex) between 16 October and 15 November 2008 using the US Department of Energy (DOE) G-1 aircraft. The objective of these flights was to gain an understanding of the sources and evolution of these aerosols, and of how they interact with the marine stratus cloud layer that prevails in this region of the globe. Our measurements showed that the marine boundary layer (MBL) aerosol mass was dominated by non-sea-salt SO42−, followed by Na+, Cl, Org (total organics), NH4+, and NO3, in decreasing order of importance; CH3SO3 (MSA), Ca2+, and K+ rarely exceeded their limits of detection. Aerosols were strongly acidic with a NH4+ to SO42− equivalents ratio typically < 0.3. Sea-salt aerosol (SSA) particles, represented by NaCl, exhibited Cl deficits caused by both HNO3 and H2SO4, but for the most part were externally mixed with particles, mainly SO42−. SSA contributed only a small fraction of the total accumulation mode particle number concentration. It was inferred that all aerosol species (except SSA) were of predominantly continental origin because of their strong land-to-sea concentration gradient. Comparison of relative changes in median values suggests that (1) an oceanic source of NH3 is present between 72° W and 76° W, (2) additional organic aerosols from biomass burns or biogenic precursors were emitted from coastal regions south of 31° S, with possible cloud processing, and (3) free tropospheric (FT) contributions to MBL gas and aerosol concentrations were negligible. The very low levels of CH3SO3 observed as well as the correlation between SO42− and NO3 (which is thought primarily anthropogenic) suggest a limited contribution of DMS to SO42− aerosol production during VOCALS.

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