Atmos. Chem. Phys., 11, 8847-8860, 2011
www.atmos-chem-phys.net/11/8847/2011/
doi:10.5194/acp-11-8847-2011
© Author(s) 2011. This work is distributed
under the Creative Commons Attribution 3.0 License.
Investigating organic aerosol loading in the remote marine environment
K. Lapina1, C. L. Heald1, D. V. Spracklen2, S. R. Arnold2, J. D. Allan3, H. Coe3, G. McFiggans3, S. R. Zorn4,*, F. Drewnick4, T. S. Bates5, L. N. Hawkins6, L. M. Russell6, A. Smirnov7, C. D. O'Dowd8, and A. J. Hind9
1Dept. of Atmospheric Science, Colorado State University, Fort Collins, CO, USA
2University of Leeds, Leeds, UK
3The University of Manchester, Manchester, UK
4Max Planck Institute for Chemistry, Mainz, Germany
5Pacific Marine Environmental Laboratory, NOAA, Seattle, WA, USA
6Scripps Institution of Oceanography, University of California at San Diego, La Jolla, CA, USA
7NASA/Goddard Space Flight Center, Greenbelt, MD, USA
8School of Physics and Centre for Climate and Air Pollution Studies, National University of Ireland Galway, Galway, Ireland
9Bigelow Laboratory for Ocean Sciences, West Boothbay Harbor, ME, USA
*now at: Harvard University, Cambridge, MA, USA

Abstract. Aerosol loading in the marine environment is investigated using aerosol composition measurements from several research ship campaigns (ICEALOT, MAP, RHaMBLe, VOCALS and OOMPH), observations of total AOD column from satellite (MODIS) and ship-based instruments (Maritime Aerosol Network, MAN), and a global chemical transport model (GEOS-Chem). This work represents the most comprehensive evaluation of oceanic OM emission inventories to date, by employing aerosol composition measurements obtained from campaigns with wide spatial and temporal coverage. The model underestimates AOD over the remote ocean on average by 0.02 (21 %), compared to satellite observations, but provides an unbiased simulation of ground-based Maritime Aerosol Network (MAN) observations. Comparison with cruise data demonstrates that the GEOS-Chem simulation of marine sulfate, with the mean observed values ranging between 0.22 μg m−3 and 1.34 μg m−3, is generally unbiased, however surface organic matter (OM) concentrations, with the mean observed concentrations between 0.07 μg m−3 and 0.77 μg m−3, are underestimated by a factor of 2–5 for the standard model run. Addition of a sub-micron marine OM source of approximately 9 TgC yr−1 brings the model into agreement with the ship-based measurements, however this additional OM source does not explain the model underestimate of marine AOD. The model underestimate of marine AOD is therefore likely the result of a combination of satellite retrieval bias and a missing marine aerosol source (which exhibits a different spatial pattern than existing aerosol in the model).

Citation: Lapina, K., Heald, C. L., Spracklen, D. V., Arnold, S. R., Allan, J. D., Coe, H., McFiggans, G., Zorn, S. R., Drewnick, F., Bates, T. S., Hawkins, L. N., Russell, L. M., Smirnov, A., O'Dowd, C. D., and Hind, A. J.: Investigating organic aerosol loading in the remote marine environment, Atmos. Chem. Phys., 11, 8847-8860, doi:10.5194/acp-11-8847-2011, 2011.
 
Search ACP
Final Revised Paper
PDF XML
Citation
Discussion Paper
Share