Abstract

Abstract. The indirect effect of aerosols on climate is highly uncertain and limits our ability to assess anthropogenic climate change. The foundation of this uncertainty is uncertainty in the number of cloud condensation nuclei (CCN), which itself stems from uncertainty in aerosol nucleation, primary emission and growth rates. In this paper, we use a global general circulation model with aerosol microphysics to assess how the uncertainties in aerosol nucleation, emission and growth rates affect our prediction of CCN(0.2%) concentrations. Using several nucleation rate parameterizations that span six orders of magnitude of globally averaged nucleation rates, the tropospheric average CCN(0.2%) concentrations vary by 17% and the boundary layer average vary by 12%. This sensitivity of tropospheric average CCN(0.2%) to the nucleation parameterizations increases to 33% and 20% when the total primary emissions are reduced by a factor of 3 and the SOA condensation rates are increased by a factor of 3.5, respectively. These results show that it is necessary to better understand global nucleation rates when determining CCN concentrations. When primary emissions rates are varied by a factor of 3 while using a binary nucleation parameterization, tropospheric average CCN(0.2%) concentrations also vary by 17%, but boundary layer average vary by 40%. Using the fastest nucleation rate parameterization, these changes drop to 3% and 22%, respectively. These results show the importance of reducing uncertainties in primary emissions, which appear from these results to be somewhat more important for CCN than the much larger uncertainties in nucleation. These results also show that uncertainties in nucleation and primary emissions are more important when sufficient condensable material is available to grow them to CCN sizes. The percent change in CCN(0.2%) concentration between pre-industrial times and present day does not depend greatly on the nucleation rate parameterization used for our base case scenarios; however, because other factors, such as primary emissions and SOA, are uncertain in both time periods, this may be a coincidence.

Highlights

  • Atmospheric aerosols are important to climate because they scatter and absorb radiation and affect the radiative properties of clouds

  • This suggests that the anthropogenic indirect forcing may not be sensitive to the nucleation mechanism; as shown in the previous sections, the effect of nucleation rate on present day cloud condensation nuclei (CCN) depends on primary emissions and secondary organic aerosol (SOA), which are both uncertain, so this insensitivity may be a coincidence

  • We evaluated the uncertainty in CCN(0.2%) concentrations due to uncertainty in the nucleation and primary emission rates in a general circulation model with online size-resolved aerosol microphysics

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Summary

Introduction

Atmospheric aerosols are important to climate because they scatter and absorb radiation and affect the radiative properties of clouds. Global atmospheric models with online aerosol microphysics have been used to predict the time and location dependent aerosol size distributions (Ghan et al, 2001; Wilson et al, 2001; Adams and Seinfeld, 2002; Adams and Seinfeld, 2003; Easter et al, 2004; Rodriguez and Dabdub, 2004; Spracklen et al, 2005b; Spracklen et al, 2005a; Stier et al, 2005; Pierce and Adams, 2006; Spracklen et al, 2006; Stier et al, 2006; Pierce et al, 2007; Spracklen et al, 2008) These models provide a tool for evaluating the connection between nucleation/emissions and the concentrations of CCN in the global atmosphere.

Overview
Changes to previous version of model
Nucleation mechanisms
Present-day emissions
Pre-industrial emissions
Simulations
Aerosol number budgets
Comparison of aerosol number to observations
A B OECD
Nucleation with base-case present-day emissions
Contribution of primary emissions to CCN
Sensitivity to SOA production rates
Pre-industrial simulations
Conclusions
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