Introduction
Since the early 1980s significant losses in stratospheric ozone have been observed in the Antarctic spring . The low temperatures (below 195 ) in the polar winter induce the formation of polar stratospheric clouds in the 15–21 altitude region, on which chlorine and bromine are activated; when the sun returns over the region, the chlorine- and bromine-induced catalytic ozone loss takes place. Since the 1970s, anthropogenic activities have gradually increased the concentrations of ozone-depleting substances (ODSs) in the atmosphere, including chlorine- and bromine-containing compounds, until they peaked around 2000 in the polar regions. The springtime ozone loss, therefore, has correspondingly increased since the late 1980s and was saturated by the early 1990s . In the Southern Hemisphere, the land and ocean contrast is smaller than in the Northern Hemisphere, and, hence, the generation and propagation of large-amplitude planetary waves are not very effective. Therefore, the polar vortex that forms in fall and winter in the stratosphere is relatively undisturbed and stable, and typically lasts for more than 7 (May–November) months. These dynamical conditions further aggravate the ozone loss in the southern polar vortex region. Because of the suppressed wave and dynamical disturbances, and the concomitant stability of the polar vortex, the interannual variation in Antarctic ozone loss since the 1990s has been small.
Large variability in Antarctic ozone loss has been seen in the last few years (2004–2013) relative to other winters since 1992 (e.g., ). For instance, the winters of 2004, 2010, and 2012 were relatively warm, with minor warmings and, hence, limited ozone loss . The first fortnight of August 2005 was unusually cold and showed a high rate of ozone loss and an unprecedented ozone hole . The winter of 2006 was one of the coldest and, hence, the Antarctic vortex experienced the largest ozone hole to date . The winters of 2007, 2009, and 2013 were characterized by average temperatures and, hence, ozone holes of a moderate size . However, the winters of 2008 and 2011 were again very cold and characterized by large ozone holes . Here, we provide a detailed view of these 10 winters in relation to polar processing and the chemistry of ozone loss. In this study, we discuss (i) the interannual variability in ozone loss and chlorine activation and (ii) horizontal, vertical, and seasonal variability in ozone loss in the Antarctic stratosphere during these (2004–2013) winters. We use high-resolution simulations for analyzing the polar processing and interannual changes in ozone loss in detail. Note that the simulations are highly resolved in the lower stratosphere (about 0.5 between 425 and 550 ) too, to closely study the ozone loss features in those peak ozone loss altitude layers. Additionally, the past 10 winters offer a good opportunity to test the chemical and dynamical processes in numerical models. Furthermore, observations from the Aura microwave limb sounder (MLS) , one of the best satellite instruments currently available for sampling polar vortices, are compared to the model results. Therefore, for the first time ozone loss and chlorine activation can be studied with high-resolution measurements that have very good spatial and temporal coverage inside the Antarctic vortex. Previous satellite measurements were relatively limited to a small temporal and spatial area as far as high-latitude observations are concerned (e.g., ). While the Upper Atmosphere Research Satellite MLS had a similar latitudinal coverage, the frequency of its polar measurements was lower than that of Aura MLS (e.g., ). Therefore, the study with high-resolution simulations (both horizontally and vertically) together with the high-resolution measurements offers some new insights into the polar processing and ozone loss features of the Antarctic stratosphere.
In this article, the MIMOSA–CHIM (Modèle Isentrope du transport Méso-échelle de l'Ozone Stratosphérique par Advection avec CHEMie) chemical transport model (CTM) (e.g., ) is used to simulate the chemical constituents for the period 2004–2013. The simulated results are then compared to the Aura MLS measurements. We first look at the ozone loss evolution within different equivalent latitudes (EqLs) averaged over 10 winters in Sect. . The assessment of the interannual variability in the ozone loss, chlorine activation, and ozone loss rates during the 10 (2004–2013) winters is presented in Sect. . Finally, Sect. concludes with our main findings.
Simulations and measurements
We use the high-resolution MIMOSA–CHIM CTM for the simulations of chemical constituents (e.g., ). The model extends horizontally from 10 N to 90 S with resolution, and there are 25 isentropic vertical levels between 350 and 950 with a resolution of about 0.5–2 , depending on altitude. The model is forced by European Centre for Medium-Range Weather Forecasts (ECMWF) operational analyses. The vertical levels of this data set have been changed from 60 to 91 levels from February 2006 to May 2013 and then to 137 levels from June 2013 onward. The chemical fields used to initialize MIMOSA–CHIM each year are obtained from a long-term simulation of the REPROBUS (Reactive Processes Ruling the Ozone Budget in the Stratosphere) CTM driven by the same ECMWF analyses. The REPROBUS model is equivalent to a lower-resolution version of the MIMOSA–CHIM model, with its resolution being 22. The chemical tendencies are calculated every 15 and the output is written for every 6 . The passive tracer is initialized only once at the beginning of the simulation, and thus the ozone loss is the cumulative loss in ppmv since the beginning of the simulation. The MIMOSA–CHIM CTM uses the Middle Atmosphere Radiation Scheme (MIDRAD) . Climatological HO and CO, but interactive O fields are used for the calculation of heating rates. The kinetics data are taken from but the ClO photolysis cross sections from , with a log-linear extrapolation up to 450 . These cross sections are in good agreement with the recent ClO measurements by , which form the basis for the JPL 2011 recommendations (i.e., ). For each Antarctic winter the model was run from 1 May to 31 October.
The 10-year (2004–2013) average monthly mean ozone loss estimated at different equivalent latitude (EqL) bins (of 2) from 65 to 83 S EqL from the MIMOSA–CHIM simulations and MLS measurements. The model results are interpolated with respect to the time and location of the MLS measurements inside the vortex and then averaged for the corresponding day. The axis represents potential temperature in K. The black dotted lines represent 0 .
[Figure omitted. See PDF]
The model has detailed polar stratospheric cloud (PSC) formation and growth and sedimentation schemes. The saturation vapor pressure provided by and is used to assume the existence of nitric acid trihydrate (NAT) and ice particles, respectively. Liquid supercooled sulfuric acid aerosols, NAT, and ice particles are considered to be in equilibrium with the gas phase . Equilibrium composition and volume of binary (HSO–HO) and ternary (HNO–HSO–HO) droplets are calculated using an analytic expression given by . For NAT and ice particles, the number density is set to , and the particle diameter is calculated within the scheme from the available volume of HNO and HSO. A denitrification scheme is also incorporated to diagnose the sedimentation of HNO-containing particles. In this scheme, the NAT particles are assumed to be in equilibrium with gas phase HNO. All three types of NAT, ice, and liquid-aerosol particles are considered, and the sedimentation speed of the particles is calculated according to .
We use the Aura MLS measurements version (v) 3.3 for a comparison with simulations. The ozone measurements have a vertical resolution of 2.5–3 over 215–0.02 , and the vertical resolution of ClO measurements is about 3–3.5 over 100–1 . The time resolution of the measurements is about 3500 profiles per day. The estimated uncertainty of typical ozone and ClO retrievals is about 5–10 and 10–20 , respectively . For a comparison with the measurements, the model results (6 output) are interpolated to the measurement locations.
Results and discussion
The passive tracer method is applied to compute the ozone loss from the simulations and measurements. This requires the simulation of passive ozone (or a passive model tracer), i.e., ozone simulations without interactive chemistry. The ozone loss is computed as the difference between the modeled passive odd-oxygen tracer (defined as the sum of O, O(1D) and O3(P)) and measured or simulated ozone. To derive the ozone loss inside the vortex, we use a vortex edge criterion of 65 EqL. The following equation is used to derive the vortex-averaged ozone loss rates and production rates from the model results. where is the ozone loss or production averaged within EqL () 65 for each model vertical level () and day (). is the instantaneous ozone loss or production calculated by the model for each grid point defined by latitude () and longitude () for each and . is the sunlit hour, which is calculated with respect to solar zenith angle 95 and which varies between 0 and 1 for complete darkness to full illumination. The is computed for each model grid point (,,) and for each day using potential-vorticity (PV) data.
Ozone loss: the 2004–2013 average
To elucidate various chemical ozone loss features, we analyze the vertical distribution of the average loss in 2004–2013 for different EqL bins estimated from the model and MLS data from May to October and shown in Fig. . The EqL-based analyses extend from 65 to 83 S in 2 increments as calculated for the MLS measurements. A detailed discussion on the calculation of EqLs and determination of the polar vortex edge can be found in and references therein. The simulations show that the chemical loss starts at lower EqLs of 65–67 S at the edge of the Antarctic vortex in May, above 600 , as also shown by , , and . It moves down to the lower altitudes by July, and the loss is largest at 65–67 S EqL. The loss continues to increase in August, with the EqLs of 65 and 83 S showing the largest and smallest loss, respectively, in accordance with the increase in incidence of sunlight over the region. A clear difference in the amount of ozone loss estimated at different EqLs is well simulated. At the edge of the vortex, a maximum modeled ozone loss of 2.1 (parts per million by volume) is found around 500–550 , while in the 70–80 S EqL range the peak loss is found above 600 .
The ozone loss continues through to September, when all EqLs show a large loss. The largest modeled loss is still found in the lower EqLs of 65–69 S, reaching about 3 at 500 . The higher EqLs (77–83 S) show the smallest ozone loss and it peaks in the middle stratosphere (600 ), while other EqLs show their peak loss below 575 . Above 600 , all EqLs show a similar ozone loss of about 1.4 . The maximum loss is about 3 over 65–70 S at 500 , 2.5 over 70–75 S at 550 , 1.7 over 75–80 S at 575 , and 1.3 over 80–83 S at 600 , and thus, the altitude of maximum loss increases with EqL up to September. As expected, the maximum ozone loss is found in October, and all EqLs show more or less the same loss (about 3 ) at the peak loss altitude of around 500 . In addition, all EqLs show a more or less similar amount of ozone loss with altitude below 500 in October. Above 500 , the ozone loss shows slight differences, with the largest loss occurring at the highest EqLs, unlike in months earlier than September. Note that the ozone loss presented here is the monthly mean ozone loss, not the instantaneous loss (see later analyses in Sect. and ), which explains the large ozone loss estimated for late September and October after the chlorine activation period (mid-June to mid-September). In addition, in October, the mixing processes affecting the air mass within the vortex when the ozone loss cycles are stopped also homogenize the ozone distributions.
Evolution of polar cap (50–90 S) minimum temperature derived from the ECMWF operational analyses for each winter from 2004 to 2013 at 500 ( 19 ) potential temperature. The and thresholds are also marked.
[Figure omitted. See PDF]
The analyses with model results below 500 are in good agreement with those of the MLS measurements. Nevertheless, the loss estimated from the observations is more compact with altitude in October, and the model–measurement differences are larger in September than in other months. The comparison of ozone loss above 550 shows that the model overestimates the ozone loss there. The ozone loss of about 0.05–0.08 that is derived from the measurements in May at 360–370 is within the estimated error bars of the measurements and therefore insignificant. The differences between measurements and simulations will be discussed further in Sect. .
Interannual variations
We have discussed the general features of the measured and modeled ozone loss evolution in the Antarctic stratosphere. Now we look into the details of the interannual variations in Antarctic ozone loss. It is well-known that low temperatures initiate PSC formation, enabling chlorine activation, which then triggers ozone loss. Therefore, we first analyze the minimum temperature and meteorological situation of each winter in 2004–2013. The link between the prevailing meteorology and chlorine activation of the winters is discussed in the following section, as the amount and extent of activated chlorine are a good indicator of the yearly changes in ozone loss. The year-to-year changes in ozone loss, i.e., the vertical profile of ozone loss, column ozone loss, and the instantaneous ozone loss are discussed in detail with respect to the aforementioned factors in the subsequent sections.
Vertical distribution of the vortex-averaged (defined by EqL) ClO estimated from the MIMOSA–CHIM model and MLS measurements for the Antarctic winters 2004–2013. The model results are interpolated with respect to the time and location of the MLS measurements inside the vortex and then averaged for the corresponding day. ClO data are not available for early May 2006 and late July and early August 2007. The measurements are selected for 10:00–16:00 local solar time and solar zenith angles below 89. Both model results and MLS data are smoothed for 7 days. The axis represents potential temperature in K. The white dotted lines represent 500 (19 ) and 675 (26 ).
[Figure omitted. See PDF]
Meteorological conditions
Figure shows the minimum polar cap (50–90 S) temperature extracted from the ECMWF operational analyses for each winter since 2004 at 500 (19 ) potential temperature. In general, the winters show a minimum temperature of about 179–186 from mid-June to mid-September. Among the winters, 2004 shows relatively higher minimum temperatures in the range of 184–200 from August onward, although some days can be excluded. In 2005, the temperatures are relatively low and remained around 182 in July–September, although a minor warming is evident in June. In 2006, the temperatures are higher (around 184 ) than in other winters in late June and July, but the September and October temperatures (183–199 ) are very low. In 2007, 2008 and 2009, the evolution of temperature is very similar, but there are minor differences in the details, such as a sudden increase of about 181–183 in July in 2007. In 2010, minor warmings are apparent in early August (182–186 ) and mid-September (185–190 ). The lowest mid-August to October temperatures at this level are found in 2011 as in the case of 2006, but the highest temperatures in October are found in 2012 with values of 194–212 . In addition, the winter of 2013 shows the lowest July–August temperatures, with about 177–179 . In brief, the winters of 2004, 2010 and 2012 can be termed warm winters and 2005, 2006, 2011, and 2013 cold or very cold winters . Since the temperature evolution is between these extremes, the other winters can be called moderately cold or moderately warm. Note that the winters are categorized with respect to the temperature evolution at this particular potential temperature, and hence the classification can be slightly different at other altitude levels. Further details about the temperature distribution and meteorology of the winters of 2010–2013 can be found in .
The vortex-averaged (defined by EqL) vertical and temporal evolution of ClO, HCl, HNO, NO, O and ozone loss from the MIMOSA–CHIM model and MLS measurements. The model results are interpolated with respect to the time and location of the MLS observations inside the vortex and then averaged for the corresponding time period. The data are the average of 10 Antarctic winters (2004–2013) and are smoothed for 7 . ClO data are not available for early May 2006 and late July and early August 2007. The ClO measurements are selected for 10:00–16:00 for local solar time and solar zenith angles below 89. The axis represents potential temperature in K and is on a logarithmic scale. The white dotted lines represent 500 (19 ) and 675 (26 ).
[Figure omitted. See PDF]
Activated chlorine
Figure compares the simulated and measured ClO at the MLS sampling points inside the vortex, defined here by the area within 65–90 S EqL and with a solar zenith angle (SZA) of less than 89, for the Antarctic winters of 2004–2013. In MIMOSA–CHIM, relatively high chlorine activation is found in 2005, when a maximum of 1.6–1.8 (parts per billion by volume) is simulated from June to late July and early August, consistent with the lower temperatures in that winter . The other winters show a more or less similar distribution of ClO and thus, chlorine activation, except in the warm winters of 2010 and 2012. The simulated ClO stands in contrast to the temperature structure and PSC observations in each winter , which showed the largest areas of PSCs in the coldest winters of 2005 and 2006. It should be noted that chlorine activation does not depend only on temperature and the occurrence of PSCs but also on the available chlorine reservoirs, which vary from one year to the next . However, when we examine the MLS measurements, they mostly follow the temperature history of each winter, as the observations show the strongest chlorine activation in 2005 and 2006 and the weakest in 2010 and 2012. The highest ClO values ( ) are found from July to the end of September over 450–600 in the colder winters but around 550 episodically in July–August in the warmer winters in the observations. Therefore, in contrast to the model results, the vortex-averaged MLS measurements display a clear interannual variation in the chlorine activation. These comparisons show that the model underestimates the observed ClO over the 450–600 range.
Vertical distribution of the vortex-averaged (defined by EqL) ozone loss estimated for the Antarctic winters in 2004–2013. The model results are interpolated with respect to the time and location of the MLS measurements inside the vortex and then averaged for the corresponding day. Left: the ozone loss derived from the difference between the passive ozone and the chemically integrated ozone by MIMOSA–CHIM. Right: the ozone loss derived from the difference between the MIMOSA–CHIM passive ozone and the ozone measured by MLS. Both model results and MLS data are smoothed for 7 days. The axis represents potential temperature in K. The white dotted lines represent 500 (19 ) and 675 (26 ).
[Figure omitted. See PDF]
In order to find out the reasons for the differences between simulated and measured ClO, we compared the simulated HCl, NO, and HNO with the MLS observations. Figure illustrates the 10-year average of the vortex mean (defined by EqL) ClO, HCl, HNO, NO, O and ozone loss from the MIMOSA–CHIM simulations and MLS measurements. The NO comparisons show that the simulated values are higher than the measured ones, as illustrated by the 50 and 100 isopleths. This bias in the simulations implies that the vertical diabatic descent in the model is slower than that deduced from MLS observations in polar spring. Consequently, the Cl and thus ClO in the model are relatively smaller. Therefore, the available chlorine or HCl for conversion to activated ClO is smaller in the model. The HCl comparison corroborates this feature of the simulations, as HCl is smaller in the simulations than in the measurements in early and midwinter and in late spring in the lower stratosphere. The deficiency in the vertical descent in the model has clearly affected the ozone simulations. For instance, the statistics of the ozone comparison reveal that the differences in May are negligible at all altitudes. In June–August, the model underestimates the measured ozone by about 0.2–0.5 below 500 . In September–October, the model overestimates (0.2–0.4 ) the measured ozone below 450 , with a peak at around 400 . However, this overestimation is well below the peak ozone loss altitudes. Above 500 , the model consistently underestimates the measured ozone from about 0.2 in June to 0.5–1 in August–October. Hence the differences at these altitudes are also qualitatively consistent with the slower vertical descent of ozone in the model.
A simulation with a different ClO recombination rate constant ( instead of the JPL recommendation, as suggested by ), was performed to test the sensitivity of the simulations and to diagnose whether the new simulations reduce the model–measurement differences. However, the ClO results did not improve significantly and hence the original simulations are presented. The HNO comparisons also indicate that the denitrification in the model is overestimated, due to the equilibrium PSC scheme of the model, as it forms large NAT particles too readily, causing more sedimentation of PSCs and thus more denitrification.
Note that the relatively low model top could also influence the slower descent or vertical transport in the model. A detailed discussion of the differences in measured and modeled ClO and HCl, chlorine partitioning in the model, and the influence of the lower model top in the simulated results will be presented in a separate paper. Also, there can be small interannual differences in the diabatic descent, depending on the accuracy of the wind fields. These have to be kept in mind while interpreting the simulations. However, in a similar study, compared the MLS measurements to SLIMCAT (Single Layer Isentropic Model for Chemistry And Transport) model results and found that their simulations slightly overestimate the ClO measurements for the Antarctic winters of 2004 and 2005. They attributed these differences to the equilibrium PSC scheme of the model. In contrast, our model ClO results underestimate the observations, although using a very similar PSC scheme. It suggests that even if the models use similar PSC schemes, the difference in model dynamics can induce significant changes in the simulated results. Nevertheless, note that the model has performed better in northern hemispheric simulations, where the ClO simulations overestimate the MLS measurements in the 2011 winter but slightly underestimate them in 2005–2010 .
Ozone loss: vertical and temporal features
Figure shows the vortex-averaged ozone loss estimated from the model and MLS at the MLS sampling locations inside the vortex in 2004–2013. As discussed in Sect. , the ozone loss onset (i.e., ozone loss 0.5 ) in the model occurs in mid-June at altitudes above 550 and gradually moves down to the lower stratosphere by mid-August. The loss intensifies by mid-August, peaks by late September–early October and slows down thereafter as the ozone recovers through dynamical processes.
Vortex-averaged (defined by EqL) column ozone loss computed from the MIMOSA–CHIM model simulations and MLS measurements, during the maximum ozone loss period in the Antarctic, at 350–850 and 400–600 for the 2004–2013 period. The estimated uncertainty of the column loss computed from both simulations and measurements is about 10 (e.g., ).
[Figure omitted. See PDF]
In the simulations, as expected, the colder winters of 2005 and 2006 show the early onset of ozone loss, in mid-June. The estimated loss is less than 0.5 above 675 until mid-August, increases to 1–1.5 by mid-September in the lower stratosphere, and peaks at 2.5–3.6 over 450–600 by early October, consistent with the temporal and vertical extent of activated ClO in these winters. A maximum ozone loss of around 3.5 is derived around 550 in 2005–2006 and about 3 around 500 in 2007, 2008 and 2011. A smaller ozone loss is found in the warmer winters of 2004, 2010 and 2012, where the peak loss is about 2.6 , around 475 . A similar range of ozone loss, but in a slightly broader vertical extent of 450–600 , is simulated in 2009 and 2013. Therefore, the center of the peak ozone loss altitude (i.e., loss ) also shows corresponding variations in agreement with the meteorology of the winters, as it is located around 550 in very cold winters (e.g., 2005 and 2006), around 500 in moderately cold winters (e.g., 2007), and around 475 in warm winters (e.g., 2004 and 2012).
Vortex-averaged (defined by EqL) chemical ozone loss and production rates at 675 ( 26 ) and 500 (19 ) in ppbv per sunlit hour (ppbv ) for the Antarctic winters 2004–2013 estimated from the MIMOSA–CHIM model simulations.
[Figure omitted. See PDF]
In general, the timing and vertical range of ozone loss in the simulations are similar to those of the observations. The modeled ozone loss onset is in mid-June, except for the colder winters (when it is in mid-May), as discussed previously, and the loss strengthens by August–September and reaches a maximum in early to mid-October, consistent with the maxima of the observations. The large ozone losses observed above 550 in September–October in the colder winters (e.g., 2005, 2006, 2007, 2008, and 2011) are also reproduced by the model. In contrast to the observed loss, the simulated ozone loss in 2007 is slightly higher than that of 2005, consistent with the temperature during these years at 500 K. However, the model consistently overestimates the measured ozone loss in the middle stratosphere in all years by about 0.2–0.5 in spring, as the model underestimates the measured ozone by the same amount at these altitudes, primarily due to the slower descent in the model during the period as discussed before. Therefore, the interannual variations are more prominent in the measurements than in the model simulations. Note that since the same passive model tracer affected by the slower diabatic descent in spring is used to derive ozone loss from the measurements, the measured ozone loss is also overestimated. Both the simulations and measurements, however, provide consistent results for the peak ozone loss altitudes in each winter.
The ozone loss derived from the SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) ozone profiles using the vortex descent method shows comparable values to that of the simulations and MLS data for the Antarctic winters of 2004–2008 . There is also good agreement in peak ozone loss values (around 3–3.5 ) and the differences in the altitudes of maximum loss for various winters. In addition, the large loss above 500 found in the model and MLS data is also inferred from the SCIAMACHY measurements.
Partial column ozone loss
In order to gain further insights into the interannual variability in ozone loss, we now analyze the column ozone loss derived from simulations and measurements. Since there are also other published results available for comparisons, analyzing partial column loss will assist with the interpretation of interannual changes. We have calculated the column ozone loss from the simulations and observations at the MLS footprints inside the vortex for each winter for the complete altitude range of the model and for the altitude region over which peak loss occurs (400–600 ); results are given in Fig. . The ozone loss as computed are the average over the maximum loss period in the Antarctic; from late September to early October (25 September–5 October). The simulated results show the lowest ozone loss in 2004 and the highest in 2005 at 350–850 , depending on the meteorology and chlorine activation during the winters. However, note that the ozone hole in 2006 was record-breaking, but both the model simulations and measurements show only slightly lower total column ozone loss compared to 2005, due to the comparatively larger chlorine activation in early winter in 2005, as also illustrated in Fig. (see the difference in chlorine activation in 2006 and 2005). Large ozone loss of about 167 is also simulated in the winter of 2007 due to relatively strong chlorine activation in that winter (Fig. ). The other winters show a column ozone loss of about DU over the same altitude range. On the other hand, the ozone loss derived from MLS observations shows the highest column ozone loss of about 162–166 in the very cold winters of 2005 and 2006 and the lowest of around 127–134 in the moderately cold winter of 2013 and the warm winters of 2010 and 2012 at 350–850 ; these are in agreement with the meteorology of the winters. Despite the differences in the values, the ozone column loss computed for 400–600 also shows similar patterns as those discussed for the 350–850 range. Note that there was strong and prolonged chlorine activation in the coldest winter of 2006 (i.e., ClO was enhanced for slightly longer in this winter than in most other winters). Also, showed that there was unusually strong chlorine activation in the lowermost stratosphere (around 375 ) that contributed to the record-setting ozone hole and ozone loss in that winter. Therefore, the data exhibit a clear interannual variation of ozone column loss as discussed for the ozone loss profile comparisons in Sect. .
The average partial column ozone depletion above the 550 level computed from the model and data for the 10 winters is about DU. This column ozone loss has to be considered when deriving partial column loss from profiles. This is slightly different from the Arctic, where significant ozone loss occurs mostly in the lower stratosphere over 350–550 in colder winters and where the depletion above 550 is limited to DU . The larger Antarctic ozone column loss contribution from higher altitudes (above 550 ) is consistent with the loss estimated above these altitudes, as shown by the ozone profiles in this study for 2004–2013 and in and for a range of Antarctic winters prior to 2004. It is also evident from the maximum ozone loss altitudes, as most Antarctic winters have their peak loss altitudes around 525 as opposed to 475 in the Arctic (e.g., ).
The partial column loss estimated from the Halogen Occultation Experiment ozone measurements ( DU) over 350–600 is larger than our results for 2004. Our loss estimates over 350–850 for 2004–2010 are in reasonable agreement with those derived from ground-based and other satellite total ozone observations in the Antarctic . The ozone loss computed from a bias-corrected satellite data set using a parameterized tracer by for the winter of 2004 also shows a similar estimate. The slight differences amongst various ozone loss values can be due to the differences in the altitude of ozone loss estimates, vortex definition, vortex sampling, and the method used to quantify the loss by the respective studies.
Ozone loss and production rates
The interannual variability in ozone loss is further analyzed with the ozone loss and production rates in the model simulations. Figure shows the instantaneous loss and production rates at 675 and 500 . In general, at 500 , the loss rates are about 2–3 (ppbv/sunlit hour) in mid-June during the onset of ozone loss, about 3–4 in July as the loss advances to the vortex core (i.e., inside the vortex at higher EqLs) and about 4–5 from August to mid-September during the peak loss period. The loss rates decrease from late September onward and reach 0 by mid-October and stay at near-zero values thereafter. Since the loss rate during the mid-September to October period depends on photochemical ozone production and loss, interannual variability is small in that period, and most winters show loss rates of about 2–5 . However, significant year-to-year variations are noted from mid-June to mid-August, as the loss rate depends on the chlorine activation and, hence, on the meteorology of the winters.
The very cold winter of 2006 exhibits an extended period of loss rates of about 4 until early October, while the winter of 2009 shows the shortest span of high loss rates, only until mid-August. The colder winter of 2008 also exhibits high loss rates in most months, May–August in particular. In some winters (e.g., 2004 and 2008) the loss rates in August are also higher than those in September. The lidar measurements of in the Antarctic winters of 1992–1998, and model studies of and in the Antarctic winter of 2003, also show comparable loss rates at 475 . Our analyses are consistent with the loss rates found in the very cold Arctic winters (1994/1995, 1999/2000, 2004/2005, and 2010/2011) during the peak loss rate period in January–February, for which loss rates of about 5–8 around 450–500 are estimated . No significant ozone production is found at this altitude level.
At 675 , large interannual variability is found in the ozone loss rates from June to August, which are about 2–5 , depending on the day of year and winter. The loss rates are typically about 2 in September and then increase rapidly to 4–6 thereafter. For instance: in 2005, the largest ozone loss rates of 3–5 are simulated in early winter, whereas about 3 is calculated in 2008. The lowest loss rates (about 1–2 ) among the 10 winters during the ozone hole period (June–September) are found in the warm winters of 2010 and 2012. Note that a similar range of loss rates of 2–7 is also calculated for the colder Arctic winters in late March and mid- to late April in 2010/2011, February–March in 2008/2009 and March in 2004/2005, depending on the day of year .
The production rates at 675 show large variations from one year to the next, from 0 in mid-August to 7 in late October. These substantial production rates in the September–October period offset the large loss rates during the same period. The high production rates at the end of winter are expected as small disturbances (toward the final warming) shift the polar vortices to sunlit parts of the midlatitudes. The analyses of the ozone production and loss rates at 675 imply that the ozone loss in the middle stratosphere also depends on the position of the polar vortex in sunlight and the dynamics of the winter.
Conclusions
The interannual variability in the Antarctic winter meteorology was relatively large in the last decade (2004–2013), which included an extremely cold winter (2006), three moderately cold winters (2005, 2008, and 2011), and three warm winters (2004, 2010, and 2012). As analyzed from the average of the 10 winter simulations, ozone loss in the Antarctic starts at the edge of the vortex at low EqLs (65–67 EqL) by mid-June, consistent with the findings of . Ozone loss progresses with time and advances to higher EqLs (69–83 EqL), with the largest loss at lower EqLs (65–69 EqL) in June–August in agreement with the exposure of the vortex to sunlight. The maximum ozone loss is attained in the mid-September to mid-October period. The peak ozone loss ( ) is found over a broad altitude range of 475–550 . The maximum modeled ozone loss is about 3.5 around 550 in 2005 and 2006, the coldest winters with the largest loss. In contrast, the maximum loss in the warmer winters of 2004, 2010 and 2012 was restricted to 2.6 . The modeled column loss shows the largest value of 173 in 2005 and the lowest of 110 in 2004 over 350–850 , consistent with the meteorology of the winters. The comparison between simulated and observed trace gas evolution during the winters suggests that the diabatic descent during spring is slower in the model. Therefore, the amount of chlorine available to be activated in spring is lower and hence, the simulated ClO is smaller than the measurements in the lower stratosphere below 550 , leading to less simulated chemical ozone loss. However, the slower descent also leads to less ozone-rich air being brought down from above. Simulated ozone values reflect a balance between these two effects.
In the lower stratosphere at 500 , the ozone loss rates have a comparable distribution in all winters, with about 2–3 in July and 4–5 from August to late September. However, as expected, the very cold winters are characterized by slightly larger and extended periods of high loss rates. In the middle stratosphere at 675 , a loss rate of about 2–5 in July–September, and a production rate of about 4–9 in September–October, are simulated. Therefore, these higher production rates largely outweigh the loss rates during the same period.
Our study finds large interannual variability in Antarctic ozone loss in the recent decade with a number of winters showing shallow ozone holes but also with the year with the maximum ozone hole in the last decades. These smaller ozone holes or ozone losses are mainly related to the year-to-year changes in dynamical processes rather than the variations in anthropogenic ODSs, as the change in ODS levels during the study period was very small.
Acknowledgements
The authors would like to thank Cathy Boonne of IPSL/CNRS for the REPROBUS model data. Work at the Jet Propulsion Laboratory, California Institute of Technology, was done under contract to NASA. The ECMWF data are obtained from the NADIR database of NILU and we greatly appreciate access to them. The work is supported by funds from the ANR/ORACLE–O France, the EU SCOUT–O and the FP7 RECONCILE project under the grant number: RECONCILE-226365-FP7-ENV-2008-1. Edited by: F. Khosrawi
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2015. This work is published under http://creativecommons.org/licenses/by/3.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
A detailed analysis of the polar ozone loss processes during 10 recent Antarctic winters is presented with high-resolution MIMOSA–CHIM (Modèle Isentrope du transport Méso-échelle de l'Ozone Stratosphérique par Advection avec CHIMie) model simulations and high-frequency polar vortex observations from the Aura microwave limb sounder (MLS) instrument. The high-frequency measurements and simulations help to characterize the winters and assist the interpretation of interannual variability better than either data or simulations alone. Our model results for the Antarctic winters of 2004–2013 show that chemical ozone loss starts in the edge region of the vortex at equivalent latitudes (EqLs) of 65–67
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details
; Godin-Beekmann, S 2 ; Lefèvre, F 2
; Santee, M L 3 ; Froidevaux, L 3 ; Hauchecorne, A 2
1 UPMC Université de Paris 06, UMR 8190 LATMOS-IPSL, CNRS/INSU, 75005 Paris, France; CORAL, Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India
2 UPMC Université de Paris 06, UMR 8190 LATMOS-IPSL, CNRS/INSU, 75005 Paris, France
3 JPL/NASA, California Institute of Technology, Pasadena, California, USA





