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  • 1
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 19, No. 2 ( 2019-01-22), p. 767-783
    Abstract: Abstract. Despite the recently reported beginning of a recovery in global stratospheric ozone (O3), an unexpected O3 decline in the tropical mid-stratosphere (around 30–35 km altitude) was observed in satellite measurements during the first decade of the 21st century. We use SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) measurements for the period 2004–2012 to confirm the significant O3 decline. The SCIAMACHY observations show that the decrease in O3 is accompanied by an increase in NO2. To reveal the causes of these observed O3 and NO2 changes, we performed simulations with the TOMCAT 3-D chemistry-transport model (CTM) using different chemical and dynamical forcings. For the 2004–2012 time period, the TOMCAT simulations reproduce the SCIAMACHY-observed O3 decrease and NO2 increase in the tropical mid-stratosphere. The simulations suggest that the positive changes in NO2 (around 7 % decade−1) are due to similar positive changes in reactive odd nitrogen (NOy), which are a result of a longer residence time of the source gas N2O and increased production via N2O + O(1D). The model simulations show a negative change of 10 % decade−1 in N2O that is most likely due to variations in the deep branch of the Brewer–Dobson Circulation (BDC). Interestingly, modelled annual mean “age of air” (AoA) does not show any significant changes in transport in the tropical mid-stratosphere during 2004–2012. However, further analysis of model results demonstrates significant seasonal variations. During the autumn months (September–October) there are positive AoA changes that imply transport slowdown and a longer residence time of N2O allowing for more conversion to NOy, which enhances O3 loss. During winter months (January–February) there are negative AoA changes, indicating faster N2O transport and less NOy production. Although the variations in AoA over a year result in a statistically insignificant linear change, non-linearities in the chemistry–transport interactions lead to a statistically significant negative N2O change.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2019
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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  • 2
    In: AIP Advances, AIP Publishing, Vol. 12, No. 12 ( 2022-12-01)
    Type of Medium: Online Resource
    ISSN: 2158-3226
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2022
    detail.hit.zdb_id: 2583909-3
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  • 3
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 22, No. 2 ( 2022-01-19), p. 903-916
    Abstract: Abstract. Until now our understanding of the 11-year solar cycle signal (SCS) in stratospheric ozone has been largely based on high-quality but sparse ozone profiles from the Stratospheric Aerosol and Gas Experiment (SAGE) II or coarsely resolved ozone profiles from the nadir-viewing Solar Backscatter Ultraviolet Radiometer (SBUV) satellite instruments. Here, we analyse 16 years (2005–2020) of ozone profile measurements from the Microwave Limb Sounder (MLS) instrument on the Aura satellite to estimate the 11-year SCS in stratospheric ozone. Our analysis of Aura-MLS data suggests a single-peak-structured SCS profile (about 3 % near 4 hPa or 40 km) in tropical stratospheric ozone, which is significantly different to the SAGE II and SBUV-based double-peak-structured SCS. We also find that MLS-observed ozone variations are more consistent with ozone from our control model simulation that uses Naval Research Laboratory (NRL) v2 solar fluxes. However, in the lowermost stratosphere modelled ozone shows a negligible SCS compared to about 1 % in Aura-MLS data. An ensemble of ordinary least squares (OLS) and three regularised (lasso, ridge and elastic net) linear regression models confirms the robustness of the estimated SCS. In addition, our analysis of MLS and model simulations shows a large SCS in the Antarctic lower stratosphere that was not seen in earlier studies. We also analyse chemical transport model simulations with alternative solar flux data. We find that in the upper (and middle) stratosphere the model simulation with Solar Radiation and Climate Experiment (SORCE) satellite solar fluxes is also consistent with the MLS-derived SCS and agrees well with the control simulation and one which uses Spectral and Total Irradiance Reconstructions (SATIRE) solar fluxes. Hence, our model simulation suggests that with recent adjustments and corrections, SORCE data can be used to analyse effects of solar flux variations. Furthermore, analysis of a simulation with fixed solar fluxes and one with fixed (annually repeating) meteorology confirms that the implicit dynamical SCS in the (re)analysis data used to force the model is not enough to simulate the observed SCS in the middle and upper stratospheric ozone. Finally, we argue that the overall significantly different SCS compared to previous estimates might be due to a combination of different factors such as much denser MLS measurements, almost linear stratospheric chlorine loading changes over the analysis period, variations in the stratospheric dynamics as well as relatively unperturbed stratospheric aerosol layer that might have influenced earlier analyses.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2022
    detail.hit.zdb_id: 2092549-9
    detail.hit.zdb_id: 2069847-1
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  • 4
    In: Earth System Science Data, Copernicus GmbH, Vol. 13, No. 12 ( 2021-12-10), p. 5711-5729
    Abstract: Abstract. High-quality stratospheric ozone profile data sets are a key requirement for accurate quantification and attribution of long-term ozone changes. Satellite instruments provide stratospheric ozone profile measurements over typical mission durations of 5–15 years. Various methodologies have then been applied to merge and homogenise the different satellite data in order to create long-term observation-based ozone profile data sets with minimal data gaps. However, individual satellite instruments use different measurement methods, sampling patterns and retrieval algorithms which complicate the merging of these different data sets. In contrast, atmospheric chemical models can produce chemically consistent long-term ozone simulations based on specified changes in external forcings, but they are subject to the deficiencies associated with incomplete understanding of complex atmospheric processes and uncertain photochemical parameters. Here, we use chemically self-consistent output from the TOMCAT 3-D chemical transport model (CTM) and a random-forest (RF) ensemble learning method to create a merged 42-year (1979–2020) stratospheric ozone profile data set (ML-TOMCAT V1.0). The underlying CTM simulation was forced by meteorological reanalyses, specified trends in long-lived source gases, solar flux and aerosol variations. The RF is trained using the Stratospheric Water and OzOne Satellite Homogenized (SWOOSH) data set over the time periods of the Microwave Limb Sounder (MLS) from the Upper Atmosphere Research Satellite (UARS) (1991–1998) and Aura (2005–2016) missions. We find that ML-TOMCAT shows excellent agreement with available independent satellite-based data sets which use pressure as a vertical coordinate (e.g. GOZCARDS, SWOOSH for non-MLS periods) but weaker agreement with the data sets which are altitude-based (e.g. SAGE-CCI-OMPS, SCIAMACHY-OMPS). We find that at almost all stratospheric levels ML-TOMCAT ozone concentrations are well within uncertainties of the observational data sets. The ML-TOMCAT (V1.0) data set is ideally suited for the evaluation of chemical model ozone profiles from the tropopause to 0.1 hPa and is freely available via https://doi.org/10.5281/zenodo.5651194 (Dhomse et al., 2021).
    Type of Medium: Online Resource
    ISSN: 1866-3516
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2021
    detail.hit.zdb_id: 2475469-9
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  • 5
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 2021
    In:  Geophysical Research Letters Vol. 48, No. 4 ( 2021-02-28)
    In: Geophysical Research Letters, American Geophysical Union (AGU), Vol. 48, No. 4 ( 2021-02-28)
    Abstract: Large mean Arctic ( 〉 63°N) chemical ozone destruction in 2019/20 of 78 DU, similar to other extreme cold winters in the past 2 decades Anomalously weak wintertime dynamical replenishment of only ∼60 DU contributed strongly to the very low observed ozone column in March Ozone recovery caused 20 DU less mean Arctic ozone loss in March 2020 than would have occurred with stratospheric halogens at 1995 levels
    Type of Medium: Online Resource
    ISSN: 0094-8276 , 1944-8007
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2021
    detail.hit.zdb_id: 2021599-X
    detail.hit.zdb_id: 7403-2
    SSG: 16,13
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  • 6
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 126, No. 6 ( 2021-03-27)
    Abstract: Very large OClO and very low NO 2 slant columns were observed by GOME‐2A during Arctic winter 2019/20 Chemical total column ozone loss of 88 DU and 106 DU was derived from TROPOMI satellite observations and the chemical transport model Chemical ozone loss derived from OMPS‐LP satellite data reached 2.1 ppmv (80%) near the 450 K potential temperature level (∼18 km)
    Type of Medium: Online Resource
    ISSN: 2169-897X , 2169-8996
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2021
    detail.hit.zdb_id: 710256-2
    detail.hit.zdb_id: 2016800-7
    detail.hit.zdb_id: 2969341-X
    SSG: 16,13
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