Satellite observations of stratospheric carbonyl fluoride

The vast majority of emissions of fluorine-containing molecules are anthropogenic in nature, e.g. chlorofluorocarbons (CFCs), hydrochlorofluorocarbons (HCFCs), and hydrofluorocarbons (HFCs). These molecules slowly degrade in the atmosphere, leading to the formation of HF, COF2, and COClF, which are...

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Autors principals: Harrison, J, Chipperfield, M, Dudhia, A, Cai, S, Dhomse, S, Boone, C, Bernath, P
Format: Journal article
Idioma:English
Publicat: Copernicus GmbH 2014
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author Harrison, J
Chipperfield, M
Dudhia, A
Cai, S
Dhomse, S
Boone, C
Bernath, P
author_facet Harrison, J
Chipperfield, M
Dudhia, A
Cai, S
Dhomse, S
Boone, C
Bernath, P
author_sort Harrison, J
collection OXFORD
description The vast majority of emissions of fluorine-containing molecules are anthropogenic in nature, e.g. chlorofluorocarbons (CFCs), hydrochlorofluorocarbons (HCFCs), and hydrofluorocarbons (HFCs). These molecules slowly degrade in the atmosphere, leading to the formation of HF, COF2, and COClF, which are the main fluorine-containing species in the stratosphere. Ultimately both COF2 and COClF further degrade to form HF, an almost permanent reservoir of stratospheric fluorine due to its extreme stability. Carbonyl fluoride (COF2) is the second-most abundant stratospheric "inorganic" fluorine reservoir, with main sources being the atmospheric degradation of CFC-12 (CCl2F2), HCFC-22 (CHF2Cl), and CFC-113 (CF2ClCFCl2). This work reports the first global distributions of carbonyl fluoride in the Earth's atmosphere using infrared satellite remote-sensing measurements by the Atmospheric Chemistry Experiment Fourier transform spectrometer (ACE-FTS), which has been recording atmospheric spectra since 2004, and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) instrument, which recorded thermal emission atmospheric spectra between 2002 and 2012. The observations reveal a high degree of seasonal and latitudinal variability over the course of a year. These have been compared with the output of SLIMCAT, a state-of-the-art three-dimensional chemical transport model. In general the observations agree well with each other, although MIPAS is biased high by as much as ∼30%, and compare well with SLIMCAT. Between January 2004 and September 2010 COF2 grew most rapidly at altitudes above ∼25 km in the southern latitudes and at altitudes below ∼25 km in the northern latitudes, whereas it declined most rapidly in the tropics. These variations are attributed to changes in stratospheric dynamics over the observation period. The overall COF2 global trend over this period is calculated as 0.85 ± 0.34 (MIPAS), 0.30 ± 0.44 (ACE), and 0.88% year-1 (SLIMCAT).
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spelling oxford-uuid:8d917b48-e50b-432e-9450-0ef09c71cfe92022-03-26T22:52:01ZSatellite observations of stratospheric carbonyl fluorideJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:8d917b48-e50b-432e-9450-0ef09c71cfe9EnglishSymplectic Elements at OxfordCopernicus GmbH2014Harrison, JChipperfield, MDudhia, ACai, SDhomse, SBoone, CBernath, PThe vast majority of emissions of fluorine-containing molecules are anthropogenic in nature, e.g. chlorofluorocarbons (CFCs), hydrochlorofluorocarbons (HCFCs), and hydrofluorocarbons (HFCs). These molecules slowly degrade in the atmosphere, leading to the formation of HF, COF2, and COClF, which are the main fluorine-containing species in the stratosphere. Ultimately both COF2 and COClF further degrade to form HF, an almost permanent reservoir of stratospheric fluorine due to its extreme stability. Carbonyl fluoride (COF2) is the second-most abundant stratospheric "inorganic" fluorine reservoir, with main sources being the atmospheric degradation of CFC-12 (CCl2F2), HCFC-22 (CHF2Cl), and CFC-113 (CF2ClCFCl2). This work reports the first global distributions of carbonyl fluoride in the Earth's atmosphere using infrared satellite remote-sensing measurements by the Atmospheric Chemistry Experiment Fourier transform spectrometer (ACE-FTS), which has been recording atmospheric spectra since 2004, and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) instrument, which recorded thermal emission atmospheric spectra between 2002 and 2012. The observations reveal a high degree of seasonal and latitudinal variability over the course of a year. These have been compared with the output of SLIMCAT, a state-of-the-art three-dimensional chemical transport model. In general the observations agree well with each other, although MIPAS is biased high by as much as ∼30%, and compare well with SLIMCAT. Between January 2004 and September 2010 COF2 grew most rapidly at altitudes above ∼25 km in the southern latitudes and at altitudes below ∼25 km in the northern latitudes, whereas it declined most rapidly in the tropics. These variations are attributed to changes in stratospheric dynamics over the observation period. The overall COF2 global trend over this period is calculated as 0.85 ± 0.34 (MIPAS), 0.30 ± 0.44 (ACE), and 0.88% year-1 (SLIMCAT).
spellingShingle Harrison, J
Chipperfield, M
Dudhia, A
Cai, S
Dhomse, S
Boone, C
Bernath, P
Satellite observations of stratospheric carbonyl fluoride
title Satellite observations of stratospheric carbonyl fluoride
title_full Satellite observations of stratospheric carbonyl fluoride
title_fullStr Satellite observations of stratospheric carbonyl fluoride
title_full_unstemmed Satellite observations of stratospheric carbonyl fluoride
title_short Satellite observations of stratospheric carbonyl fluoride
title_sort satellite observations of stratospheric carbonyl fluoride
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