Atmos. Chem. Phys. Discuss., 11, 18853-18899, 2011
www.atmos-chem-phys-discuss.net/11/18853/2011/
doi:10.5194/acpd-11-18853-2011
© Author(s) 2011. This work is distributed
under the Creative Commons Attribution 3.0 License.
Review Status
This discussion paper has been under review for the journal Atmospheric Chemistry and Physics (ACP). Please refer to the corresponding final paper in ACP.
Global distribution and climate forcing of marine organic aerosol – Part 1: Model improvements and evaluation
N. Meskhidze1, J. Xu1,2, B. Gantt1, Y. Zhang1, A. Nenes3,4, S. J. Ghan5, X. Liu5, R. Easter5, and R. Zaveri5
1Department of Marine, Earth, and Atmospheric Sciences, North Carolina State University, Raleigh, NC, USA
2Chinese Research Academy of Environment Sciences, No. 8 Dayangfang, Beiyuan, Chaoyang District, Beijing 100012, China
3School of Earth and Atmospheric Sciences, Georgia Institute of Technology, Atlanta, GA, USA
4School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, USA
5Atmospheric Sciences & Global Change Division, Pacific Northwest National Laboratory, Richland, WA, USA

Abstract. Marine organic aerosol emissions have been implemented and evaluated within the National Center of Atmospheric Research (NCAR)'s Community Atmosphere Model (CAM5) with the Pacific Northwest National Laboratory's 7-mode Modal Aerosol Module (MAM-7). Emissions of marine primary organic aerosols (POA), phytoplankton-produced isoprene- and monoterpenes-derived secondary organic aerosols (SOA) and methane sulfonate (MS) are shown to affect surface concentrations of organic aerosols in remote marine regions. Global emissions of submicron marine POA is estimated to be 7.9 and 9.4 Tg yr−1, for the Gantt et al. (2011) and Vignati et al. (2010) emission parameterizations, respectively. Marine sources of SOA and particulate MS (containing both sulfur and carbon atoms) contribute an additional 0.2 and 5.1 Tg yr−1, respectively. Widespread areas over productive waters of the Northern Atlantic, Northern Pacific, and the Southern Ocean show marine-source submicron organic aerosol surface concentrations of 100 ng m−3, with values up to 400 ng m−3 over biologically productive areas. Comparison of long-term surface observations of water insoluble organic matter (WIOM) with POA concentrations from the two emission parameterizations shows that both Gantt et al. (2011) and Vignati et al. (2010) formulations are able to capture the magnitude of marine organic aerosol concentrations, with the Gantt et al. (2011) parameterization attaining better seasonality. Model simulations show that the mixing state of the marine POA can impact the surface number concentration of cloud condensation nuclei (CCN). The largest increases (up to 20 %) in CCN (at a supersaturation (S) of 0.2 %) number concentration are obtained over biologically productive ocean waters when marine organic aerosol is assumed to be externally mixed with sea-salt. Assuming marine organics are internally-mixed with sea-salt provides diverse results with increase and decrease in the concentration of CCN over different parts of the ocean. The sign of the CCN change due to the addition of marine organics to sea-salt aerosol is determined by the relative significance of the increase in mean modal diameter due to addition of mass, and the decrease in particle hygroscopicity due to compositional changes in marine aerosol. Based on emerging evidence for increased CCN concentration over biologically active surface ocean areas/periods, our study suggests that treatment of sea spray in global climate models (GCMs) as an internal mixture of marine organic aerosols and sea-salt will likely lead to an underestimation in CCN number concentration.

Citation: Meskhidze, N., Xu, J., Gantt, B., Zhang, Y., Nenes, A., Ghan, S. J., Liu, X., Easter, R., and Zaveri, R.: Global distribution and climate forcing of marine organic aerosol – Part 1: Model improvements and evaluation, Atmos. Chem. Phys. Discuss., 11, 18853-18899, doi:10.5194/acpd-11-18853-2011, 2011.
 
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