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Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
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Volume 13, issue 13
Atmos. Chem. Phys., 13, 6429-6430, 2013
https://doi.org/10.5194/acp-13-6429-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.
Atmos. Chem. Phys., 13, 6429-6430, 2013
https://doi.org/10.5194/acp-13-6429-2013
© Author(s) 2013. This work is distributed under
the Creative Commons Attribution 3.0 License.

Research article 08 Jul 2013

Research article | 08 Jul 2013

Corrigendum to "Aerosol indirect effects from shipping emissions: sensitivity studies with the global aerosol-climate model ECHAM-HAM" published in Atmos. Chem. Phys., 12, 5985–6007, 2012

K. Peters1,2,*, P. Stier3, J. Quaas4, and H. Graßl1 K. Peters et al.
  • 1Max Planck Institute for Meteorology, Hamburg, Germany
  • 2International Max Planck Research School on Earth System Modelling, Hamburg, Germany
  • 3Department of Physics, University of Oxford, UK
  • 4Institute for Meteorology, University of Leipzig, Leipzig, Germany
  • *now at: ARC Centre of Excellence for Climate System Science, Monash University, School of Mathematical Sciences,Clayton, VIC 3800, Australia

Abstract. An error in the calculation of the emitted number of primary sulfate particles for a given mass of emitted elementary sulfur has recently been identified in HAM, i.e. the aerosol module utilised in the ECHAM-HAM aerosol climate model. Correcting for this error substantially alters the estimates of top-of-atmosphere radiative forcing due to aerosol indirect effects from global shipping emissions (year 2000) as presented in Peters et al. (2012). Here, we shortly present these new results.

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