Abstract

Abstract. Chlorine activation in the Arctic is investigated by examining different parameterizations for uptake coefficients on stratospheric aerosols, high-resolution in-situ measurements and vortex-wide satellite observations. The parameterizations for heterogeneous chemistry on liquid aerosols are most sensitive to temperature with the reaction rates doubling for every 1 K increase in temperature. However, differences between the currently available parameterizations are negligible. For Nitric Acid Trihydrate particles (NAT) the major factors of uncertainty are the number density of nucleated particles and different parameterizations for heterogeneous chemistry. These two factors induce an uncertainty that covers several orders of magnitude on the reaction rate. Nonetheless, since predicted reaction rates on liquid aerosols always exceed those on NAT, the overall uncertainty for chlorine activation is small. In-situ observations of ClOx from Arctic winters in 2005 and 2010 are used to evaluate the heterogeneous chemistry parameterizations. The conditions for these measurements proved to be very different between those two winters with HCl being the limiting reacting partner for the 2005 measurements and ClONO2 for the 2010 measurements. Modeled levels of chlorine activation are in very good agreement with the in-situ observations and the surface area provided by Polar Stratospheric Clouds (PSCs) has only a limited impact on modeled chlorine activation. This indicates that the parameterizations give a good representation of the processes in the atmosphere. Back-trajectories started on the location of the observations in 2005 indicate temperatures on the threshold for PSC formation, hence the surface area is mainly provided by the background aerosol. Still, the model shows additional chlorine activation during this time-frame, providing cautionary evidence for chlorine activation even in the absence of PSCs. Vortex-averaged satellite observations by the MLS instrument also show no definite connection between chlorine activation and PSC formation. The inter -and intra-annual variability of vortex-average HCl and HNO3 based on MLS observations is examined for the Arctic winters 2004/2005 to 2010/2011. These observations show that removal of HCl and HNO3 from the gas-phase are not correlated. HNO3 loss exhibits great inter-annual variability depending on prevailing temperatures while HCl loss is continuous through December without considerable inter- or intra-annual variability. Only the recovery of HCl in late winter depends on the level of denitrification. Hence, the occurrence of HNO3 containing PSC particles does not seem to have a significant effect on the speed of initial chlorine activation on a vortex-wide scale.

Highlights

  • During polar night in the stratosphere the main chlorine reservoir species HCl and ClONO2 are converted to photolabile species through heterogeneous reactions on liquid and solid particles (Solomon et al, 1986), a process known as chlorine activation

  • We have examined the importance of the stratospheric background aerosol for chlorine activation

  • Even though Nitric Acid Trihydrate (NAT) and Supercooled Ternary Solution (STS) could form under the prevailing conditions the additional surface area provided by Polar Stratospheric Clouds (PSCs) does not significantly enhance chlorine activation. 90% of activated chlorine during this time-frame originate from heterogeneous chemistry on a surface area provided by the background aerosol

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Summary

Introduction

During polar night in the stratosphere the main chlorine reservoir species HCl and ClONO2 are converted to photolabile species through heterogeneous reactions on liquid and solid particles (Solomon et al, 1986), a process known as chlorine activation. The liquid and solid particles acting as reactions sites for heterogeneous chemistry are provided by Polar Stratospheric Clouds (PSCs) and the ubiquitous background sulfate aerosol layer. Kawa et al (1997) reported in-situ measurements of active chlorine from the Antarctic during the ASHOE/MAESA campaign in 1994 where backtrajectories indicated that during the ten days prior to the measurements, temperatures had been too high for PSC formation and concluded that the observed chlorine activation must have occurred on the background aerosol. The following sections will discuss the existing parameterizations for heterogeneous chemistry on the various aerosol types and their uncertainty These parameterizations are validated with in-situ measurements and the role of the background aerosol is constrained with model simulations and satellite observations

Chlorine Activation
In situ observations
Binary only
Vortex average
Findings
Conclusions
Full Text
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