Abstract

Abstract. The eruption of Mount Pinatubo produced the largest loading of stratospheric sulphate aerosol in the twentieth century. This heated the tropical lower stratosphere, affecting stratospheric circulation, and provided enhanced surface area for heterogeneous chemistry. These factors combined to produce record low values of "global" total ozone column. Though well studied, there remains some uncertainty about the attribution of this low ozone, with contributions from both chemical and dynamical effects. We take a complementary approach to previous studies, nudging the potential temperature and horizontal winds in the new UKCA chemistry climate model to reproduce the atmospheric response and assess the impact on global total ozone. We then combine model runs and observations to distinguish between chemical and dynamical effects. To estimate the effects of increased heterogeneous chemistry on ozone we compare runs with volcanically enhanced and background surface aerosol density. The modelled depletion of global ozone peaks at about 7 DU in early 1993, in good agreement with values obtained from observations. We subtract the modelled aerosol induced ozone loss from the observed ozone record and attribute the remaining variability to `dynamical' effects. The remaining variability is dominated by the QBO. We also examine tropical and mid-latitude ozone, diagnosing contributions from El Niño in the tropics and identifying dynamically driven low ozone in northern mid-latitudes, which we interpret as possible evidence of changes in the QBO. We conclude that, on a global scale, the record lows of extra-polar ozone are produced by the increased heterogeneous chemistry, although there is evidence for dynamics produced low ozone in certain regions, including northern mid-latitudes.

Highlights

  • The eruption of Mount Pinatubo injected 20 Tg of SO2 into the stratosphere which was, on the time-scales of weeks, converted into sulphate aerosol

  • 3 Results anQalByOsibsadsaetdaoaznodneapsriomxpyl(e7 pmroesnctrhisp)tion of increased surface aerosol density used in Run A produces a good representation of global ozone variability

  • 3.1 Validation of UKCA-6global ozone column ozone data are used in the ERA-40 assimilation over this period (Dethof and Holm, 2004) this good correspondence may be expected even though we neglect other factors, such as changes in chlorine loading and solar UV flux

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Summary

Introduction

The eruption of Mount Pinatubo injected 20 Tg of SO2 into the stratosphere which was, on the time-scales of weeks, converted into sulphate aerosol. The direct chemical effect was a result of the aerosol surface acting as sites for heterogeneous chemical reactions (Solomon, 1999) This locked NOx into inactive HNO3, liberating chlorine from reservoirs to active species, enabling the catalytic destruction of ozone (Fahey et al, 1993; Solomon, 1999; Robock, 2000). The temperature increases in the lower and middle stratosphere were significant, with peak increases at 30 hPa of around 3.5 K (Labitzke and McCormick, 1992) This positive anomaly gradually decreased over the course of 1992 as the tropical aerosol was dispersed (McCormick et al, 1995). The associated subsidence at high latitudes brought ozone down, potentially masking some of the destruction by chemical processes (Robock, 2000)

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