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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