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100 CHAPTER 2. ATMOSPHERE AND REMOTE SENSING<br />

2.6.2 Ozone Depletion Events in the Polar Boundary Layer in Spring: A<br />

Model Study<br />

Participating scientists Matthias Piot and Roland von Glasow<br />

Abstract For more than 20 years, events with almost complete loss of ozone have been observed<br />

in the Arctic in spring. The importance of several species and meteorological parameters for these<br />

depletions have been investigated with sensitivity studies using a numerical box model.<br />

Figure 2.56: Schematic depiction of the most important processes included in the MISTRA model, applied<br />

for Arctic conditions. Fluxes over ice and sea salt production are switched ON/OFF, depending<br />

on the air composition we study.<br />

Background Reactive halogens play a major<br />

role in polar ozone depletion events (ODE): the<br />

reaction of bromine atoms with ozone, followed<br />

by the self-reaction of bromine oxides (BrO) represents<br />

a catalytic loss mechanism for ozone in the<br />

polar boundary layer (PBL). However, the triggering<br />

of the so-called ”bromine explosion” remains<br />

unclear. I present model results where prescribed<br />

bromine or chlorine fluxes are used to reproduce<br />

ODEs. I investigated the importance of several<br />

compounds for the chemistry of the PBL as well as<br />

meteorological parameters and focused on species<br />

which influence the occurrence of an ODE. This<br />

study allows us to better understand which species<br />

are important in the process of depleting ozone.<br />

Funding DFG: Emmy Noether Junior Research<br />

Group MarHal GL 353/1-1<br />

Methods and results I used the chemical and<br />

microphysical model MISTRA in the lagrangian<br />

box-model mode to study the mechanisms influencing<br />

these observed depletions in the polar<br />

boundary layer. My sensitivity studies consisted<br />

of a set of four-day runs where I changed initial<br />

mixing ratios or fluxes (or both) of 19 different<br />

species (including halogens, NOx, NOy,<br />

DMS, H2O2, HCHO...) and compared the results<br />

with base runs. The influence of temperature<br />

and humidity have also been examined. High<br />

HCHO concentrations result via increases in HO2<br />

in a redistribution of bromine species involving<br />

the aerosol phase, slowing ODEs down. Elevated<br />

DMS leads to an increase in HCHO, therefore also<br />

slowing ODEs down. By a similar production of<br />

HOx, hydrogen peroxyde (H2O2) also oxidizes Brx<br />

compounds inducing an ODE slow down. The<br />

presence of both Cl2 and Br2 in the air may lead<br />

to an unexpected decrease in the destruction process,<br />

depending on their relative mixing ratios. Increasing<br />

the mixing ratio of ethane by a factor of<br />

2 reduces the ozone mixing ratio from a partial<br />

ODE to a major ODE. For cases with low Br,<br />

ethene emphasizes the ozone loss. With high Br,<br />

it reduces the destruction process. An increase in<br />

HONO led to different eventual ozone mixing ratios,<br />

depending on its use by Brx-Clx compounds.<br />

A change in temperature or humidity modifies the<br />

liquid water content of aerosols and therefore the<br />

uptake coefficients. The recycling of halogens via<br />

the liquid phase is modified.<br />

Outlook/Future work This sensitivity study<br />

will help us investigate the potential triggers like<br />

frost flowers for the bromine explosion, using MIS-<br />

TRA in the lagrangian 1D mode.<br />

Main publication Piot and von Glasow, presentations<br />

at EGU, Vienna, 2005 and OASIS<br />

workshop, Toronto, 2005

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