scholarly journals Estimation of Antarctic ozone loss from ground-based total column measurements

2010 ◽  
Vol 10 (14) ◽  
pp. 6569-6581 ◽  
Author(s):  
J. Kuttippurath ◽  
F. Goutail ◽  
J.-P. Pommereau ◽  
F. Lefèvre ◽  
H. K. Roscoe ◽  
...  

Abstract. The passive tracer method is used to estimate ozone loss from ground-based measurements in the Antarctic. A sensitivity study shows that the ozone depletion can be estimated within an accuracy of ~4%. The method is then applied to the ground-based observations from Arrival Heights, Belgrano, Concordia, Dumont d'Urville, Faraday, Halley, Marambio, Neumayer, Rothera, South Pole, Syowa, and Zhongshan for the diagnosis of ozone loss in the Antarctic. On average, the ten-day boxcar average of the vortex mean ozone column loss deduced from the ground-based stations was about 55±5% in 2005–2009. The ozone loss computed from the ground-based measurements is in very good agreement with those derived from satellite measurements (OMI and SCIAMACHY) and model simulations (REPROBUS and SLIMCAT), where the differences are within ±3–5%. The historical ground-based total ozone observations in October show that the depletion started in the late 1970s, reached a maximum in the early 1990s and stabilised afterwards due to saturation. There is no indication of ozone recovery yet. At southern mid-latitudes, a reduction of 20–50% is observed for a few days in October–November at the newly installed Rio Gallegos station. Similar depletion of ozone is also observed episodically during the vortex overpasses at Kerguelen in October–November and at Macquarie Island in July–August of the recent winters. This illustrates the significance of measurements at the edges of Antarctica.

2010 ◽  
Vol 10 (3) ◽  
pp. 7641-7674
Author(s):  
J. Kuttippurath ◽  
F. Goutail ◽  
J.-P. Pommereau ◽  
F. Lefèvre ◽  
H. K. Roscoe ◽  
...  

Abstract. The passive ozone method is used to estimate ozone loss from ground-based measurements in the Antarctic. A sensitivity study shows that the O3 loss can be estimated within an accuracy of ~4%. The method is then applied to the observations from Amundsen-Scott/South Pole, Arrival Heights, Belgrano, Concordia, Dumont d'Urville, Faraday, Halley, Marambio, Neumayer, Rothera, Syowa and Zhongshan for the diagnosis of ozone loss in the Antarctic. On average, the five-day running mean of the vortex averaged ozone column loss deduced from the ground-based stations shows about 53% in 2009, 59% in 2008, 55% in 2007, 56% in 2006 and 61% in 2005. The observed O3 loss and loss rates are in very good agreement with the satellite observations (Ozone Monitoring Instrument and Sciamachy) and are well reproduced by the model (Reprobus and SLIMCAT) calculations. The historical ground-based total ozone measurements show that the depletion started in the late 1970s, reached a maximum in the early 1990s, stabilising afterwards at this level until present, with the exception of 2002, the year of an early vortex break-up. There is no indication of significant recovery yet. At southern mid-latitudes, a total ozone reduction of 40–50% is observed at the newly installed station Rio Gallegos and 25–35% at Kerguelen in October–November of 2008–2009 and 2005–2009 (except 2008) respectively, and of 10–20% at Macquarie Island in July–August of 2006–2009. This illustrates the significance of measurements at the edges of Antarctica.


2016 ◽  
Vol 16 (24) ◽  
pp. 15619-15627 ◽  
Author(s):  
Ulrike Langematz ◽  
Franziska Schmidt ◽  
Markus Kunze ◽  
Gregory E. Bodeker ◽  
Peter Braesicke

Abstract. The year 1980 has often been used as a benchmark for the return of Antarctic ozone to conditions assumed to be unaffected by emissions of ozone-depleting substances (ODSs), implying that anthropogenic ozone depletion in Antarctica started around 1980. Here, the extent of anthropogenically driven Antarctic ozone depletion prior to 1980 is examined using output from transient chemistry–climate model (CCM) simulations from 1960 to 2000 with prescribed changes of ozone-depleting substance concentrations in conjunction with observations. A regression model is used to attribute CCM modelled and observed changes in Antarctic total column ozone to halogen-driven chemistry prior to 1980. Wintertime Antarctic ozone is strongly affected by dynamical processes that vary in amplitude from year to year and from model to model. However, when the dynamical and chemical impacts on ozone are separated, all models consistently show a long-term, halogen-induced negative trend in Antarctic ozone from 1960 to 1980. The anthropogenically driven ozone loss from 1960 to 1980 ranges between 26.4 ± 3.4 and 49.8 ± 6.2 % of the total anthropogenic ozone depletion from 1960 to 2000. An even stronger ozone decline of 56.4 ± 6.8 % was estimated from ozone observations. This analysis of the observations and simulations from 17 CCMs clarifies that while the return of Antarctic ozone to 1980 values remains a valid milestone, achieving that milestone is not indicative of full recovery of the Antarctic ozone layer from the effects of ODSs.


2016 ◽  
Author(s):  
Asen Grytsai ◽  
Gennadi Milinevsky ◽  
Andrew Klekociuk ◽  
Oleksandr Evtushevsky

Abstract. The quasi-stationary pattern of the Antarctic total ozone has changed during the last four decades, demonstrating an eastward shift in the zonal ozone minimum. In this work, the association between the longitudinal shift of the zonal ozone minimum and changes in meteorological fields in austral spring (September–November) for 1979–2014 is analyzed. Regressive, correlative and anomaly composite analyses are applied to reanalysis data. Patterns of the Southern Annular Mode and quasi-stationary zonal waves 1 and 3 in the meteorological fields show relationships with interannual variability in the longitude of the zonal ozone minimum. On decadal time scales, consistent longitudinal shifts of the zonal ozone minimum and zonal wave 3 pattern in the middle troposphere temperature at the southern mid-latitudes are shown. As known, Antarctic ozone depletion in spring is strongly projected on the Southern Annular Mode in summer and impacts tropospheric climate. The results of this study suggest that changes in zonal ozone asymmetry accompanying the ozone depletion could be associated with regional climate changes in the Southern Hemisphere in spring.


2012 ◽  
Vol 18 (5(78)) ◽  
pp. 48-58
Author(s):  
V.O. Kravchenko ◽  
O.M. Yevtushevskyi ◽  
H.P. Milinevskyi

2021 ◽  
Vol 13 (8) ◽  
pp. 1594
Author(s):  
Songkang Kim ◽  
Sang-Jong Park ◽  
Hana Lee ◽  
Dha Hyun Ahn ◽  
Yeonjin Jung ◽  
...  

The ground-based ozone observation instrument, Brewer spectrophotometer (Brewer), was used to evaluate the quality of the total ozone column (TOC) produced by multiple polar-orbit satellite measurements at three stations in Antarctica (King Sejong, Jang Bogo, and Zhongshan stations). While all satellite TOCs showed high correlations with Brewer TOCs (R = ~0.8 to 0.9), there are some TOC differences among satellite data in austral spring, which is mainly attributed to the bias of Atmospheric Infrared Sounder (AIRS) TOC. The quality of satellite TOCs is consistent between Level 2 and 3 data, implying that “which satellite TOC is used” can induce larger uncertainty than “which spatial resolution is used” for the investigation of the Antarctic TOC pattern. Additionally, the quality of satellite TOC is regionally different (e.g., OMI TOC is a little higher at the King Sejong station, but lower at the Zhongshan station than the Brewer TOC). Thus, it seems necessary to consider the difference of multiple satellite data for better assessing the spatiotemporal pattern of Antarctic TOC.


2014 ◽  
Vol 14 (19) ◽  
pp. 10431-10438 ◽  
Author(s):  
X. Yang ◽  
N. L. Abraham ◽  
A. T. Archibald ◽  
P. Braesicke ◽  
J. Keeble ◽  
...  

Abstract. Naturally produced very short-lived substances (VSLS) account for almost a quarter of the current stratospheric inorganic bromine, Bry. Following VSLS oxidation, bromine radicals (Br and BrO) can catalytically destroy ozone. The extent to which possible increases in surface emissions or transport of these VSLS bromocarbons to the stratosphere could counteract the effect of halogen reductions under the Montreal Protocol is an important policy question. Here, by using a chemistry–climate model, UM-UKCA, we investigate the impact of a hypothetical doubling (an increase of 5 ppt Bry) of VSLS bromocarbons on ozone and how the resulting ozone changes depend on the background concentrations of chlorine and bromine. Our model experiments indicate that for the 5 ppt increase in Bry from VSLS, the ozone decrease in the lowermost stratosphere of the Southern Hemisphere (SH) may reach up to 10% in the annual mean; the ozone decrease in the Northern Hemisphere (NH) is smaller (4–6%). The largest impact on the ozone column is found in the Antarctic spring. There is a significantly larger ozone decrease following the doubling of the VSLS burden under a high stratospheric chlorine background than under a low chlorine background, indicating the importance of the inter-halogen reactions. For example, the decline in the high-latitude, lower-stratospheric ozone concentration as a function of Bry is higher by about 30–40% when stratospheric Cly is ~ 3 ppb (present day), compared with Cly of ~ 0.8 ppb (a pre-industrial or projected future situation). Bromine will play an important role in the future ozone layer. However, even if bromine levels from natural VSLS were to increase significantly later this century, changes in the concentration of ozone will likely be dominated by the decrease in anthropogenic chlorine. Our calculation suggests that for a 5 ppt increase in Bry from VSLS, the Antarctic ozone hole recovery date could be delayed by approximately 6–8 years, depending on Cly levels.


1992 ◽  
Vol 338 (1285) ◽  
pp. 219-226 ◽  

Although stratospheric ozone loss had been predicted for m any years, the discovery of the Antarctic ozone hole was a surprise which necessitated a major rethink in theories of stratospheric chemistry. The new ideas advanced are discussed here. Global ozone loss has now also been reported after careful analysis of satellite and groundbased data sets. The possible causes of this loss are considered. Further advances require a careful coordination of field measurements and large-scale numerical modelling.


2021 ◽  
Author(s):  
Annika Seppälä ◽  
Emily Gordon ◽  
Bernd Funke ◽  
Johanna Tamminen ◽  
Kaley Walker

<p>We present the impact of the so-called energetic particle precipitation (EPP), part of natural solar forcing on the atmosphere, on polar stratospheric NO<sub>x</sub>, ozone, and chlorine chemistry in the Antarctic springtime, using multi-satellite observations covering the overall period of 2005–2017. We find consistent ozone increases when high solar activity occurs during years with easterly phase of the quasi biennial oscillation. These ozone enhancements are also present in total O<sub>3</sub> column observations. We find consistent decreases in springtime active chlorine following winters of elevated solar activity. Further analysis shows that this is accompanied by increase of chemically inactive chlorine reservoir species, explaining the observed ozone increase. This provides the first observational evidence supporting the previously proposed mechanism relating to EPP modulating chlorine driven ozone loss. Our findings suggest that solar activity via EPP has played an important role in modulating Antarctic ozone depletion in the last 15 years. As chlorine loading in the polar stratosphere continues to decrease in the future, this buffering mechanism will become less effective and catalytic ozone destruction by EPP produced NO<sub>x</sub> will likely become a major contributor to Antarctic ozone loss.</p>


2006 ◽  
Vol 6 (11) ◽  
pp. 3303-3314 ◽  
Author(s):  
H. K. Roscoe ◽  
J. Roscoe

Abstract. The Royal Society expedition to Antarctica established a base at Halley Bay, in support of the International Geophysical Year of 1957–1958. Surface ozone was measured during 1958 only, using a prototype Brewer-Mast sonde. The envelope of maximum ozone was an annual cycle from 10 ppbv in January to 22 ppbv in August. These values are 35% less at the start of the year and 15% less at the end than modern values from Neumayer, also a coastal site. This may reflect a general increase in surface ozone since 1958 and differences in summer at the less windy site of Halley, or it may reflect ozone loss on the inlet together with long-term conditioning. There were short periods in September when ozone values decreased rapidly to near-zero, and some in August when ozone values were rapidly halved. Such ozone-loss episodes, catalysed by bromine compounds, became well-known in the Artic in the 1980s, and were observed more recently in the Antarctic. In 1958, very small ozone values were recorded for a week in midwinter during clear weather with light winds. The absence of similar midwinter reductions at Neumayer, or at Halley in the few measurements during 1987, means we must remain suspicious of these small values, but we can find no obvious reason to discount them. The dark reaction of ozone and seawater ice observed in the laboratory may be fast enough to explain them if the salinity and surface area of the ice is sufficiently amplified by frost flowers.


2018 ◽  
Vol 11 (6) ◽  
pp. 3595-3610 ◽  
Author(s):  
Anna Vaskuri ◽  
Petri Kärhä ◽  
Luca Egli ◽  
Julian Gröbner ◽  
Erkki Ikonen

Abstract. We demonstrate the use of a Monte Carlo model to estimate the uncertainties in total ozone column (TOC) derived from ground-based direct solar spectral irradiance measurements. The model estimates the effects of possible systematic spectral deviations in the solar irradiance spectra on the uncertainties in retrieved TOC. The model is tested with spectral data measured with three different spectroradiometers at an intercomparison campaign of the research project “Traceability for atmospheric total column ozone” at Izaña, Tenerife on 17 September 2016. The TOC values derived at local noon have expanded uncertainties of 1.3 % (3.6 DU) for a high-end scanning spectroradiometer, 1.5 % (4.4 DU) for a high-end array spectroradiometer, and 4.7 % (13.3 DU) for a roughly adopted instrument based on commercially available components and an array spectroradiometer when correlations are taken into account. When neglecting the effects of systematic spectral deviations, the uncertainties reduce by a factor of 3. The TOC results of all devices have good agreement with each other, within the uncertainties, and with the reference values of the order of 282 DU during the analysed day, measured with Brewer spectrophotometer #183.


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