Department of Atmospheric, Oceanic and Space Science, University of Michigan, Ann Arbor, Michigan, USA
Received: 26 Mar 2012 – Published in Atmos. Chem. Phys. Discuss.: 19 Apr 2012
Abstract. We examine the formation of nitrate and ammonium on five types of externally mixed pre-existing aerosols using the hybrid dynamic method in a global chemistry transport model. The model developed here predicts a similar spatial pattern of total aerosol nitrate and ammonium to that of several pioneering studies, but separates the effects of nitrate and ammonium on pure sulfate, biomass burning, fossil fuel, dust and sea salt aerosols. Nitrate and ammonium boost the scattering efficiency of sulfate and organic matter but lower the extinction of sea salt particles since the hygroscopicity of a mixed nitrate-ammonium-sea salt particle is less than that of pure sea salt. The direct anthropogenic forcing of particulate nitrate and ammonium at the top of the atmosphere (TOA) is estimated to be −0.12 W m−2. Nitrate, ammonium and nitric acid gas also affect aerosol activation and the reflectivity of clouds. The first aerosol indirect forcing by anthropogenic nitrate (gas plus aerosol) and ammonium is estimated to be −0.09 W m−2 at the TOA, almost all of which is due to condensation of nitric acid gas onto growing droplets (−0.08 W m−2).
Revised: 14 Sep 2012 – Accepted: 24 Sep 2012 – Published: 22 Oct 2012
Citation: Xu, L. and Penner, J. E.: Global simulations of nitrate and ammonium aerosols and their radiative effects, Atmos. Chem. Phys., 12, 9479-9504, doi:10.5194/acp-12-9479-2012, 2012.