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  A growing threat to the ozone layer from short-lived anthropogenic chlorocarbons

Oram, D. E., Ashfold, M. J., Laube, J. C., Gooch, L. J., Humphrey, S., Sturges, W. T., et al. (2017). A growing threat to the ozone layer from short-lived anthropogenic chlorocarbons. Atmospheric Chemistry and Physics, 17(19), 11929-11941. doi:10.5194/acp-17-11929-2017.

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Oram, David E.1, Autor
Ashfold, Matthew J.1, Autor
Laube, Johannes C.1, Autor
Gooch, Lauren J.1, Autor
Humphrey, Stephen1, Autor
Sturges, William T.1, Autor
Leedham-Elvidge, Emma1, Autor
Forster, Grant L.1, Autor
Harris, Neil R. P.1, Autor
Mead, Mohammed Iqbal1, Autor
Abu Samah, Azizan1, Autor
Phang, Siew Moi1, Autor
Ou-Yang, Chang-Feng1, Autor
Lin, Neng-Huei1, Autor
Wang, Jia-Lin1, Autor
Baker, Angela K.2, Autor           
Brenninkmeijer, Carl A. M.2, Autor           
Sherry, David1, Autor
Affiliations:
1external, ou_persistent22              
2Atmospheric Chemistry, Max Planck Institute for Chemistry, Max Planck Society, ou_1826285              

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 Zusammenfassung: Large and effective reductions in emissions of long-lived ozone-depleting substance (ODS) are being achieved through the Montreal Protocol, the effectiveness of which can be seen in the declining atmospheric abundances of many ODSs. An important remaining uncertainty concerns the role of very short-lived substances (VSLSs) which, owing to their relatively short atmospheric lifetimes (less than 6 months), are not regulated under the Montreal Protocol. Recent studies have found an unexplained increase in the global tropospheric abundance of one VSLS, dichloromethane (CH2Cl2), which has increased by around 60 % over the past decade. Here we report dramatic enhancements of several chlorine-containing VSLSs (Cl-VSLSs), including CH2Cl2 and CH2ClCH2Cl (1,2-dichloroethane), observed in surface and upper-tropospheric air in East and South East Asia. Surface observations were, on occasion, an order of magnitude higher than previously reported in the marine boundary layer, whilst upper-tropospheric data were up to 3 times higher than expected. In addition, we provide further evidence of an atmospheric transport mechanism whereby substantial amounts of industrial pollution from East Asia, including these chlorinated VSLSs, can rapidly, and regularly, be transported to tropical regions of the western Pacific and subsequently uplifted to the tropical upper troposphere. This latter region is a major provider of air entering the stratosphere, and so this mechanism, in conjunction with increasing emissions of Cl-VSLSs from East Asia, could potentially slow the expected recovery of stratospheric ozone.

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Sprache(n): eng - English
 Datum: 2017
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: ISI: 000412845500001
DOI: 10.5194/acp-17-11929-2017
 Art des Abschluß: -

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Titel: Atmospheric Chemistry and Physics
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: Katlenburg-Lindau, Germany : European Geosciences Union
Seiten: - Band / Heft: 17 (19) Artikelnummer: - Start- / Endseite: 11929 - 11941 Identifikator: ISSN: 1680-7316
CoNE: https://pure.mpg.de/cone/journals/resource/111030403014016