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Original Articles

A meridional profile of the chemical composition of submicrometre particles over the East Atlantic Ocean: regional and hemispheric variabilities

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Pages 377-394 | Received 18 May 2001, Accepted 18 Apr 2002, Published online: 15 Dec 2016

References

  • Artaxo, P., Gerab, F., Yamasoe, M. A. and Martins, J. V. 1994. Fine mode aerosol composition at three long-term atmospheric monitoring sites in the amazon basin. J. Geophys. Res. 99, D11, 22,857-22,868.
  • Ayers, G. P., Ivey, J. P. and Gillett, R. W. 1991. Coher-ence between seasonal cycles of dimethyl sulphide, methanesulphonate and sulphate in marine air. Nature 349, 404–406.
  • Ayers, G. P., Cainey, J. M., Granek, H. and Leck, C. 1996. Dimethylsulfide oxidation and the ratio of meth-anesulfonate to non sea-salt sulfate in the marine aero-sol. J. Atmos. Chem. 25, 307–325.
  • Bates, T. S., Calhoun, J. A. and Quinn, P. K. 1992. Variations in the methanesulfonate to sulfate molar ratio in submicrometer marine aerosol particles over the South Pacific Ocean. J. Geophys. Res. 97, D9, 9859–9865.
  • Bilrgermeister, S., Zimmermann, R. L., Georgii, H.-W., Bingemer, H. G., Kirst, G. O., Janssen, M. and Ernst, W. 1990. On the biogenic origin of dimethylsul-fide: relation between chlorophyll, ATP, organismic DMSP, phytoplankton species, and DMS distribution in Atlantic surface water and atmosphere. J. Great Lakes Res. 95, 20,607-20,615.
  • Charlson, R. J., Langner, J., Rodhe, H., Leovy, C. B. and Warren, S. G. 1991. Perturbation of the northern hemi-sphere radiative balance by backscattering of anthro-pogenic sulfate aerosols. Tellus 43AB, 152-163.
  • Covert, D. S. 1988. North Pacific marine background aerosol: average ammonium to sulfate molar ratio equals 1. J. Geophys. Res. 93, D7, 8455–8458.
  • Davison, B., Hewitt, C. N., O'Dowd, C. D., Lowe, J. A., Smith, M. H., et al. 1996a. Dimethyl sulfide, methane sulfonic acid and physicochemical aerosol properties in Atlantic air from the United Kingdom to Halley Bay. J. Geophys. Res. 101, D17, 22,855-22,867.
  • Davison, B., O'Dowd, C., Hewitt, C. N., Smith, M. H., Harrison, R. M., et al. 1996b. Dimethyl sulfide and its oxidation products in the atmosphere of the Atlantic and Southern Oceans. Atmos. Environ. 30, 1895–1906.
  • Engardt, M. and Rodhe, H. 1993. A comparison between patterns of temperature trends and sulfate aerosol pollution. Geophys. Res. Lett. 20, 117–120.
  • Gillespie, J. B. and Lindberg, J. D. 1992. Ultraviolet and visible imaginary refractive index of strongly absorb-ing atmospheric particulate matter. Appl. Opt. 31, 2112–2115.
  • Hansson, H.-C., Martinsson, B. G., Swietlicki, E., Asking, L., Heintzenberg, J. and Ogren, J. A. 1986. PIXE in complex analytical systems for atmospheric chemistry. Nucl. Instr. Meth. 22B, 235-240.
  • Heintzenberg, J. 1982. Size-segregated measurements of particulate elemental carbon and aerosol light absorp-tion at remote Arctic locations. Atmos. Environ. 16, 2461–2469.
  • Heintzenberg, J. 1988. A processor-controlled multisam-ple soot photometer. Aerosol Sci. Technol. 8, 227–233.
  • Heintzenberg, J., Covert, D. S. and Van Dingenen, R. 2000. Size distribution and chemical composition of marine aerosols: compilation and review. Tellus 52B, 1104–1122.
  • Herman, J. R., Bhartia, P. K., Torres, O., Hsu, C., Seftor, C. and Celarier, E. 1997. Global distribution of UV-absorbing aerosols from Nimbus 7/TOMS data, 1997. J. Geophys. Res. 102, D14, 16,911-16,922.
  • Johansson, T. B., Akselsson, R. and Johansson, S. A. E. 1970. X-ray analysis: elemental trace analysis at the 10' g level. Nucl. Instr. Meth. 84, 141–143.
  • Junge, C. and Jaenicke, R. 1971. New results in back-ground aerosols studied from the Atlantic expedition of the R.V. Meteor, spring 1969. J. Aerosol Sci. 2, 305–314.
  • Karl, T. R., Knight, R. W., Kukla, G. and Gavin, J. 1995. Evidence for radiative effects of anthropogenic sulfate aerosols in the observed climate record. In: Aerosol forcing of climate (eds. R. J. Charlson and J. Heintzen-berg), John Wiley & Sons, New York, 363-384.
  • Kerker, M., Schemer, P., Cooke, D. D. and Kratohvil, J. P. 1979. Absorption index and color of colloidal hematite. J. Colloid Interface Sci. 71, 176–187.
  • Kiehl, J. T. and Rodhe, H. 1995. Modeling geographical and seasonal forcing due to aerosols. In: Aerosol forcing of climate (eds. R. J. Charlson and J. Heintzen-berg), John Wiley & Sons, New York, 281-296.
  • Kiehl, J. T., Schneider, T. L., Portmann, R. W. and Solomon, S. 1999. Climate forcing due to tropospheric and stratospheric ozone. J. Geophys. Res. 104, D24, 31,239-31,254.
  • Kiehl, J. T., Schneider, T. L., Rasch, P. J., Barth, M. C. and Portman, R. W. 2000. Radiative forcing due to sulfate aerosols from simulations with the NCAR com-munity climate model (CCM3). J. Geophys. Res. 105, 1441–1457.
  • Langner, J. and Rodhe, H. 1991. A global three-dimensional model of the tropospheric sulfur cycle. J. Atmos. Chem. 13, 225–264.
  • Leck, C., Norman, M., Bigg, E. K. and Hillamo, R. 2002. Chemical composition and sources of the high Arctic aerosol relevant for cloud formation. J. Geophys. Res., in press.
  • Leck, C. and Persson, C. 1996. Seasonal and short-term variability in dimethyl sulfide, sulfur dioxide and bio-genic sulfur and sea salt aerosol particles in the Arctic marine boundary layer during summer and autumn. Tellus 48B, 272–299.
  • Liousse, C., Penner, J. E., Chuang, C., Walton, J. J. and Eddleman, H. 1996. A global three-dimensional model study of carbonaceous aerosols. J. Geophys. Res. 101, D14, 19,411-19,432.
  • McGrath, R. 1989. Trajectory models and their use in the Irish Meteorological Service. 112/89, Irish Meteoro-logical Service, Dublin.
  • Neustllg, C., Weise, D., Birmili, W., Wex, H., Wieden-sohler, A. and Covert, D. S. 2000. Size-segregated chemical, gravimetric and number distribution-derived mass closure of the aerosol in Sagres, Portugal during ACE-2. Tellus 52B, 169-184.
  • Noone, K. J. and Hansson, H.-C. 1990. Calibration of the TSI-3760 condensation nucleus counter for non-standard operating conditions. Aerosol Sci. Technol. 13, 478–485.
  • Ogren, J. A. and Heintzenberg, J. 1990. Parametric aerosol sampling at low concentration levels. AA-1, Department of Meteorology, Stockholm University.
  • Penner, J. E. 1995. Carbonaceous aerosols influencing atmospheric radiation: black and organic carbon. In: Aerosol forcing of climate (eds. R. J. Charlson and J. Heintzenberg), John Wiley & Sons, New York, 91-108.
  • Penner, J. E., Dickinson, R. E. and O'Neill, C. A. 1992. Effects of aerosol from biomass burning on the global radiation budget. Science 256, 1432–1434.
  • Rahn, K. A. 1976. The chemical composition of the atmo-spheric aerosol. Graduate School of Oceanography, University of Rhode Island, Kingston, RI, USA. Roeckner, E., Siebert, T. and Feichter, J. 1995. Climatic response to anthropogenic sulfate forcing simulated with a general circulation model. In: Aerosol forcing of climate (eds. R. J. Charlson and J. Heintzenberg), John Wiley & Sons, New York, 349-362.
  • Saxena, V. K. 1983. Evidence of biogenic nuclei involve-ment in Antarctic coastal clouds. J. Phys. Chem. 87, 4130–4134.
  • Taylor, K. E. and Penner, J. E. 1994. Response of the climate system to atmospheric aerosols and green-house gases. Nature 369, 734–737.
  • Taylor, S. R. 1964. Abundance of chemical elements in the continental crust: a new table. Geochim. Cosmo-chim. Acta 28, 1273–1285.
  • Wilson, T. R. S. 1975. Salinity and major elements of seawater. In: Chemical oceanography (eds. J. P. Riley and G. Skirrow), 2nd edn. Academic Press, Orlando, FL, 365-413.