001     22111
005     20240712100909.0
024 7 _ |2 DOI
|a 10.5194/angeo-30-1055-2012
024 7 _ |2 WOS
|a WOS:000306975300003
024 7 _ |2 Handle
|a 2128/7505
037 _ _ |a PreJuSER-22111
041 _ _ |a eng
082 _ _ |a 550
084 _ _ |2 WoS
|a Astronomy & Astrophysics
084 _ _ |2 WoS
|a Geosciences, Multidisciplinary
084 _ _ |2 WoS
|a Meteorology & Atmospheric Sciences
100 1 _ |0 P:(DE-HGF)0
|a Drdla, K.
|b 0
245 _ _ |a Temperature thresholds for chlorine activation and ozone loss in the polar stratosphere
260 _ _ |a Kaltenburg, Lindau
|b Copernicus
|c 2012
300 _ _ |a 1055 - 1073
336 7 _ |a Journal Article
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336 7 _ |a article
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440 _ 0 |0 419
|a Annales Geophysicae-Atmospheres, Hydrospheres and Space Sciences
|v 30
|x 0992-7689
500 _ _ |3 POF3_Assignment on 2016-02-29
500 _ _ |a We are grateful to Dave Fahey, Jens-Uwe Grooss, Thomas Peter, Bob Portmann, Ross Salawitch, Susan Solomon, Simone Tilmes, and Tobias Wegner for very helpful discussions and for constructive critical comments. We thank Thomas Peter, Ross Salawitch, Susan Solomon and a number of anonymous referees for their thoughtful reviews. We also thank Tobias Wegner very much for providing Figs. 1 and 2. This research was supported in part by NASA's Earth Science Enterprise through the Atmospheric Chemistry and Modeling Analysis Program, NRA-02-OES-02 and by the European Union EU-FP7-226365-RECONCILE grant. We are grateful to the United Kingdom Met Office for providing meteorological analyses.
520 _ _ |a Low stratospheric temperatures are known to be responsible for heterogeneous chlorine activation that leads to polar ozone depletion. Here, we discuss the temperature threshold below which substantial chlorine activation occurs. We suggest that the onset of chlorine activation is dominated by reactions on cold binary aerosol particles, without the formation of polar stratospheric clouds (PSCs), i.e. without any significant uptake of HNO3 from the gas phase. Using reaction rates on cold binary aerosol in a model of stratospheric chemistry, a chlorine activation threshold temperature, T-ACL, is derived. At typical stratospheric conditions, T-ACL is similar in value to T-NAT (within 1-2 K), the highest temperature at which nitric acid trihydrate (NAT) can exist. T-NAT is still in use to parameterise the threshold temperature for the onset of chlorine activation. However, perturbations can cause T-ACL to differ from T-NAT: T-ACL is dependent upon H2O and potential temperature, but unlike T-NAT is not dependent upon HNO3. Furthermore, in contrast to T-NAT, T-ACL is dependent upon the stratospheric sulfate aerosol loading and thus provides a means to estimate the impact on polar ozone of strong volcanic eruptions and some geo-engineering options, which are discussed. A parameterisation of T-ACL is provided here, allowing it to be calculated for low solar elevation (or high solar zenith angle) over a comprehensive range of stratospheric conditions. Considering T-ACL as a proxy for chlorine activation cannot replace a detailed model calculation, and polar ozone loss is influenced by other factors apart from the initial chlorine activation. However, T-ACL provides a more accurate description of the temperature conditions necessary for chlorine activation and ozone loss in the polar stratosphere than T-NAT.
536 _ _ |a Atmosphäre und Klima
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536 _ _ |a RECONCILE - Reconciliation of essential process parameters for an enhanced predictability of arctic stratospheric ozone loss and its climate interactions. (226365)
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|f FP7-ENV-2008-1
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653 2 0 |2 Author
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653 2 0 |2 Author
|a composition and chemistry
700 1 _ |0 P:(DE-Juel1)129138
|a Müller, R.
|b 1
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773 _ _ |0 PERI:(DE-600)1458425-6
|a 10.5194/angeo-30-1055-2012
|g Vol. 30, p. 1055 - 1073
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856 7 _ |u http://dx.doi.org/10.5194/angeo-30-1055-2012
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