Institute for Climate and Atmospheric Science, School of Earth and Environment, University of Leeds, Leeds, LS2 9JT, UK
Received: 18 Apr 2011 – Published in Atmos. Chem. Phys. Discuss.: 01 Jun 2011
Abstract. HO2 is an important atmospheric trace gas, whose sink to aerosol is poorly understood yet significant. Previous parameterisations of the rate of uptake have been limited by the lack of laboratory studies. This paper creates a parameterisation for γHO2 based on the available laboratory studies. The calculated global mean γHO2 is 0.028, significantly lower than previous work (0.2). Modelled concentrations of HO2 show significant regional sensitivity to the value of γHO2 (up to +106% at the surface with the parameterisation of γHO2 in this work as compared with a value of 0.2), but global sensitivity is small (+3.2%). The modelled response in O3 is also highly regional, being up to +27% at the surface over China, and only +0.3% globally (with the parameterisation of γHO2 in this work as compared with a value of 0.2). The impact of γHO2 on sulfate is more complex, with up to +16% over China and −5% over high latitudes, resulting in a global change of +1.2% (with the parameterisation of γHO2 in this work as compared with a value of 0.2). Uncertainty in the reaction mechanism and hence products (previously assumed to be H2O2) impacts the processing of sulfur and hence aerosol loads. Further laboratory studies are desirable to constrain the rate of reaction and to elucidate the reaction mechanism and products.
Revised: 07 Oct 2011 – Accepted: 20 Oct 2011 – Published: 04 Nov 2011
Citation: Macintyre, H. L. and Evans, M. J.: Parameterisation and impact of aerosol uptake of HO2 on a global tropospheric model, Atmos. Chem. Phys., 11, 10965-10974, doi:10.5194/acp-11-10965-2011, 2011.