Polar ozone depletion: Current status

1991 ◽  
Vol 69 (8-9) ◽  
pp. 1110-1122 ◽  
Author(s):  
G. S. Henderson ◽  
J. C. McConnell ◽  
S. R. Beagley ◽  
W. F. J. Evans
Keyword(s):  
High Latitude ◽  
Ozone Depletion ◽  
Stratospheric Ozone ◽  
Montreal Protocol ◽  
Chemical Mechanism ◽  
The Arctic ◽  
Current Status ◽  
Austral Spring ◽  
The Antarctic ◽  
Polar Ozone

Rapid springtime depletion of column ozone (O3) is observed over the Antarctic during the austral spring. A much weaker springtime depletion is observed in the Arctic region. This depletion results from a complex chemical mechanism that involves the catalytic destruction of stratospheric ozone by chlorine. The chemical mechanism appears to operate between ~12–25 km in the colder regions of the polar winter vortices. During the polar night heterogeneous chemical reactions occur on the surface of polar stratospheric clouds that convert relatively inert reservoir Cl species such as HCl to active Cl species. These clouds form when temperatures drop below about 197 K and are ubiquitous throughout the polar winter region. At polar sunrise the reactive Cl species are photolysed, liberating large quantities of free Cl that subsequently catalytically destroys O3 with a mechanism involving the formation of the Cl2O2 dimer. The magnitude of the spring depletion is much greater in the Antarctic relative to the Arctic owing to the greater stability and longer duration of the southern polar vortex. Breakup of the intense high-latitude vortices in late (Antarctic) or early (Arctic) spring results in infilling of the ozone holes but adversely affects midlatitude ozone levels by diluting them with O3-depleted, ClO-rich high-latitude air. The magnitude of the Antarctic ozone depletion has been increasing since 1979 and its current depletion in October 1990 amounts to 60%. The increase in the size of the depletion is anticorrelated with increasing anthropogenic chlorofluorocarbon (CFCs) release. Adherence to the revised Montréal Protocol should result in a reduction of stratospheric halogen levels with subsequent amelioration of polar ozone depletion but the time constant for the atmosphere to return to pre-CFC levels is ~60–100 years.

scholarly journals Reconciliation of essential process parameters for an enhanced predictability of Arctic stratospheric ozone loss and its climate interactions

2012 ◽  
Vol 12 (11) ◽  
pp. 30661-30754 ◽  
Author(s):  
M. von Hobe ◽  
S. Bekki ◽  
S. Borrmann ◽  
F. Cairo ◽  
F. D'Amato ◽  
...  
Keyword(s):  
Climate Change ◽  
Ozone Depletion ◽  
Stratospheric Ozone ◽  
Polar Vortex ◽  
The Arctic ◽  
Synoptic Scale ◽  
Ice Clouds ◽  
Ozone Loss ◽  
Process Studies ◽  
Polar Ozone

Abstract. Significant reductions in stratospheric ozone occur inside the polar vortices each spring when chlorine radicals produced by heterogeneous reactions on cold particle surfaces in winter destroy ozone mainly in two catalytic cycles, the ClO dimer cycle and the ClO/BrO cycle. Chlorofluorocarbons (CFCs), which are responsible for most of the chlorine currently present in the stratosphere, have been banned by the Montreal Protocol and its amendments, and the ozone layer is predicted to recover to 1980 levels within the next few decades. During the same period, however, climate change is expected to alter the temperature, circulation patterns and chemical composition in the stratosphere, and possible geo-engineering ventures to mitigate climate change may lead to additional changes. To realistically predict the response of the ozone layer to such influences requires the correct representation of all relevant processes. The European project RECONCILE has comprehensively addressed remaining questions in the context of polar ozone depletion, with the objective to quantify the rates of some of the most relevant, yet still uncertain physical and chemical processes. To this end RECONCILE used a broad approach of laboratory experiments, two field missions in the Arctic winter 2009/10 employing the high altitude research aircraft M55-Geophysica and an extensive match ozone sonde campaign, as well as microphysical and chemical transport modelling and data assimilation. Some of the main outcomes of RECONCILE are as follows: (1) vortex meteorology: the 2009/10 Arctic winter was unusually cold at stratospheric levels during the six-week period from mid-December 2009 until the end of January 2010, with reduced transport and mixing across the polar vortex edge; polar vortex stability and how it is influenced by dynamic processes in the troposphere has led to unprecedented, synoptic-scale stratospheric regions with temperatures below the frost point; in these regions stratospheric ice clouds have been observed, extending over >106km2 during more than 3 weeks. (2) Particle microphysics: heterogeneous nucleation of nitric acid trihydrate (NAT) particles in the absence of ice has been unambiguously demonstrated; conversely, the synoptic scale ice clouds also appear to nucleate heterogeneously; a variety of possible heterogeneous nuclei has been characterised by chemical analysis of the non-volatile fraction of the background aerosol; substantial formation of solid particles and denitrification via their sedimentation has been observed and model parameterizations have been improved. (3) Chemistry: strong evidence has been found for significant chlorine activation not only on polar stratospheric clouds (PSCs) but also on cold binary aerosol; laboratory experiments and field data on the ClOOCl photolysis rate and other kinetic parameters have been shown to be consistent with an adequate degree of certainty; no evidence has been found that would support the existence of yet unknown chemical mechanisms making a significant contribution to polar ozone loss. (4) Global modelling: results from process studies have been implemented in a prognostic chemistry climate model (CCM); simulations with improved parameterisations of processes relevant for polar ozone depletion are evaluated against satellite data and other long term records using data assimilation and detrended fluctuation analysis. Finally, measurements and process studies within RECONCILE were also applied to the winter 2010/11, when special meteorological conditions led to the highest chemical ozone loss ever observed in the Arctic. In addition to quantifying the 2010/11 ozone loss and to understand its causes including possible connections to climate change, its impacts were addressed, such as changes in surface ultraviolet (UV) radiation in the densely populated northern mid-latitudes.

scholarly journals Dynamical Mechanisms for the Recent Ozone Depletion in the Arctic Stratosphere Linked to the North Pacific Sea Surface Temperatures

2021 ◽  
Author(s):  
Dingzhu Hu ◽  
Zhaoyong Guan ◽  
Meichen Liu ◽  
Wuhu Feng
Keyword(s):  
North Pacific ◽  
Ozone Depletion ◽  
Lower Stratosphere ◽  
Stratospheric Ozone ◽  
Montreal Protocol ◽  
Sea Surface ◽  
The Arctic ◽  
The North ◽  
The Impact ◽  
The North Pacific

Abstract The ozone layer, which prevents solar ultraviolet radiation from reaching the surface and thereby protects life on earth, is expected to recover from past depletion during this century due to the impact of the Montreal Protocol. However, how the ozone column over the Arctic will evolve over the next few decades is still under debate. In this study, we found that the ozone level in the Arctic stratosphere during the period of 1998–2018 exhibits a decreasing trend of –0.12±0.07 ppmv decade–1 from MERRA2, suggesting a continued depletion during this century. This ozone depletion is contributed by the second leading mode of North Pacific sea surface temperature anomalies (SSTAs) with one month leading and therefore dynamical in origin. The North Pacific SSTAs associated with this mode tend to result in a weakened Aleutian low, a strengthened Western Pacific pattern and a weakened Pacific–North American pattern, which impede the upward propagation of planetary wavenumber-1 waves into the lower stratosphere. The changes in the stratospheric wave activity tend to result in decreased ozone in the Arctic lower stratosphere through weakening the Brewer-Dobson circulation. Our findings will provide new understanding of how dynamical processes control Arctic stratospheric ozone and will help to improve prediction of how Arctic ozone will evolve in the future.

scholarly journals A study of polar ozone depletion based on sequential assimilation of satellite data from the ENVISAT/MIPAS and Odin/SMR instruments

2007 ◽  
Vol 7 (3) ◽  
pp. 899-911 ◽  
Author(s):  
J. D. Rösevall ◽  
D. P. Murtagh ◽  
J. Urban ◽  
A. K. Jones
Keyword(s):  
Satellite Data ◽  
Ozone Depletion ◽  
Transport Model ◽  
Potential Temperature ◽  
Polar Vortex ◽  
Solar Irradiation ◽  
The Arctic ◽  
Ozone Data ◽  
The Antarctic ◽  
Polar Ozone

Abstract. The objective of this study is to demonstrate how polar ozone depletion can be mapped and quantified by assimilating ozone data from satellites into the wind driven transport model DIAMOND, (Dynamical Isentropic Assimilation Model for OdiN Data). By assimilating a large set of satellite data into a transport model, ozone fields can be built up that are less noisy than the individual satellite ozone profiles. The transported fields can subsequently be compared to later sets of incoming satellite data so that the rates and geographical distribution of ozone depletion can be determined. By tracing the amounts of solar irradiation received by different air parcels in a transport model it is furthermore possible to study the photolytic reactions that destroy ozone. In this study, destruction of ozone that took place in the Antarctic winter of 2003 and in the Arctic winter of 2002/2003 have been examined by assimilating ozone data from the ENVISAT/MIPAS and Odin/SMR satellite-instruments. Large scale depletion of ozone was observed in the Antarctic polar vortex of 2003 when sunlight returned after the polar night. By mid October ENVISAT/MIPAS data indicate vortex ozone depletion in the ranges 80–100% and 70–90% on the 425 and 475 K potential temperature levels respectively while the Odin/SMR data indicates depletion in the ranges 70–90% and 50–70%. The discrepancy between the two instruments has been attributed to systematic errors in the Odin/SMR data. Assimilated fields of ENVISAT/MIPAS data indicate ozone depletion in the range 10–20% on the 475 K potential temperature level, (~19 km altitude), in the central regions of the 2002/2003 Arctic polar vortex. Assimilated fields of Odin/SMR data on the other hand indicate ozone depletion in the range 20–30%.

scholarly journals Evaluating the Performance of Ozone Products Derived from CrIS/NOAA20, AIRS/Aqua and ERA5 Reanalysis in the Polar Regions in 2020 Using Ground-Based Observations

2021 ◽  
Vol 13 (21) ◽  
pp. 4375
Author(s):  
Hongmei Wang ◽  
Yapeng Wang ◽  
Kun Cai ◽  
Songyan Zhu ◽  
Xinxin Zhang ◽  
...  
Keyword(s):  
Ozone Depletion ◽  
Ozone Hole ◽  
Detection Sensitivity ◽  
The Arctic ◽  
Polar Regions ◽  
Loss Process ◽  
Ozone Loss ◽  
Ozone Profile ◽  
The Antarctic ◽  
Polar Ozone

Quantifying spatiotemporal polar ozone changes can promote our understanding of global stratospheric ozone depletion, polar ozone-related chemical processes, and atmospheric dynamics. By means of ground-level measurements, satellite observations, and re-analyzed meteorology, the global spatial and temporal distribution characteristics of the total column ozone (TCO) and ozone profile can be quantitatively described. In this study, we evaluated the ozone datasets from CrIS/NOAA20, AIRS/Aqua, and ERA5/ECWMF for their performance in polar regions in 2020, along with the in situ observations of the Dobson, Brewer, and ozonesonde instruments, which are regarded as benchmarks. The results showed that the ERA5 reanalysis ozone field had good consistency with the ground observations (R > 0.95) and indicated whether the TCO or ozone profile was less affected by the site location. In contrast, both CrIS and AIRS could capture the ozone loss process resulting from the Antarctic/Arctic ozone hole at a monthly scale, but their ability to characterize the Arctic ozone hole was weaker than in the Antarctic. Specifically, the TCO values derived from AIRS were apparently higher in March 2020 than those of ERA5, which made it difficult to assess the area and depth of the ozone hole during this period. Moreover, the pattern of CrIS TCO was abnormal and tended to deviate from the pattern that characterized ERA5 and AIRS at the Alert site during the Arctic ozone loss process in 2020, which demonstrates that CrIS ozone products have limited applicability at this ground site. Furthermore, the validation of the ozone profile shows that AIRS and CrIS do not have good vertical representation in the polar regions and are not able to characterize the location and depth of ozone depletion. Overall, the results reveal the shortcomings of the ozone profiles derived from AIRS and CrIS observations and the reliability of the ERA5 reanalysis ozone field in polar applications. A more suitable prior method and detection sensitivity improvement on CrIS and AIRS ozone products would improve their reliability and applicability in polar regions.

Rapid motion of the 1989 Arctic ozone crater as viewed with TOMS data

1991 ◽  
Vol 69 (8-9) ◽  
pp. 1087-1092 ◽  
Author(s):  
F. E. Bunn ◽  
F. W. Thirkettle ◽  
W. F. J. Evans
Keyword(s):  
Soviet Union ◽  
Ozone Depletion ◽  
Total Ozone ◽  
Stratospheric Ozone ◽  
Ozone Layer ◽  
The Arctic ◽  
Late Winter ◽  
Western Canada ◽  
Baffin Island ◽  
The Antarctic

The data from the NIMBUS-7 TOMS instrument were used to study the Arctic ozone layer in late winter and spring, 1989. This paper presents an analysis of TOMS total ozone values, to produce a picture of the morphology of the Arctic stratospheric ozone crater in winter–spring 1989. The Arctic crater formed in late January when the vortex moved off the pole to over Scandinavia. The TOMS data clearly show the Arctic ozone-crater feature over Scandinavia and the western Soviet Union, on February 2, 1989. It later moved south to Baffin Island and then, in March, down over Toronto, and eventually to western Canada, near Edmonton. A similar, unexpected, crater was present in the Antarctic fall, on March 15, 1989. This phenomenon is mainly produced by dynamic uplift, but there may be ozone depletion occurring as well owing to reduced temperatures.

Record springtime stratospheric ozone depletion at 80°N in 2020

2021 ◽  
Author(s):  
Ramina Alwarda ◽  
Kristof Bognar ◽  
Kimberly Strong ◽  
Martyn Chipperfield ◽  
Sandip Dhomse ◽  
...  
Keyword(s):  
Ozone Depletion ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Polar Vortex ◽  
The Arctic ◽  
Optical Absorption Spectroscopy ◽  
Chemical Transport Model ◽  
Polar Stratospheric Clouds ◽  
Ozone Loss ◽  
Stratospheric Clouds

<p>The Arctic winter of 2019-2020 was characterized by an unusually persistent polar vortex and temperatures in the lower stratosphere that were consistently below the threshold for the formation of polar stratospheric clouds (PSCs). These conditions led to ozone loss that is comparable to the Antarctic ozone hole. Ground-based measurements from a suite of instruments at the Polar Environment Atmospheric Research Laboratory (PEARL) in Eureka, Canada (80.05°N, 86.42°W) were used to investigate chemical ozone depletion. The vortex was located above Eureka longer than in any previous year in the 20-year dataset and lidar measurements provided evidence of polar stratospheric clouds (PSCs) above Eureka. Additionally, UV-visible zenith-sky Differential Optical Absorption Spectroscopy (DOAS) measurements showed record ozone loss in the 20-year dataset, evidence of denitrification along with the slowest increase of NO<sub>2</sub> during spring, as well as enhanced reactive halogen species (OClO and BrO). Complementary measurements of HCl and ClONO<sub>2</sub> (chlorine reservoir species) from a Fourier transform infrared (FTIR) spectrometer showed unusually low columns that were comparable to 2011, the previous year with significant chemical ozone depletion. Record low values of HNO<sub>3</sub> in the FTIR dataset are in accordance with the evidence of PSCs and a denitrified atmosphere. Estimates of chemical ozone loss were derived using passive ozone from the SLIMCAT offline chemical transport model to account for dynamical contributions to the stratospheric ozone budget.</p>

scholarly journals How sensitive is the recovery of stratospheric ozone to changes in concentrations of very short-lived bromocarbons?

2014 ◽  
Vol 14 (19) ◽  
pp. 10431-10438 ◽  
Author(s):  
X. Yang ◽  
N. L. Abraham ◽  
A. T. Archibald ◽  
P. Braesicke ◽  
J. Keeble ◽  
...  
Keyword(s):  
Climate Model ◽  
Stratospheric Ozone ◽  
Montreal Protocol ◽  
Background Concentrations ◽  
Future Situation ◽  
Antarctic Ozone ◽  
The Antarctic ◽  
The Impact ◽  
Ozone Column ◽  
Policy Question

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.

The Influence of Ozone Feedbacks on Surface Climate following Spring Arctic Ozone Depletion

2021 ◽  
Author(s):  
Marina Friedel ◽  
Gabriel Chiodo ◽  
Andrea Stenke ◽  
Daniela Domeisen ◽  
Stefan Muthers ◽  
...  
Keyword(s):  
Ozone Depletion ◽  
Arctic Oscillation ◽  
Stratospheric Ozone ◽  
The Arctic ◽  
Model Simulations ◽  
Temperature Anomalies ◽  
Surface Climate ◽  
Anomalous Surface ◽  
Surface Weather ◽  
Surface Patterns

<p>Links between springtime Arctic stratospheric ozone anomalies and anomalous surface weather in the Northern Hemisphere have been found recently. Stratospheric ozone thus provides valuable information which may help to improve seasonal predictability. However, the extent and causality of the ozone-surface climate coupling remain unclear and many state-of-the-art forecast models lack any representation of ozone feedbacks on planetary circulation.</p><p>We investigate the importance of the ozone-surface climate coupling with two Chemistry Climate Models, contrasting simulations with fully interactive ozone against prescribed zonally averaged climatological ozone under fixed present-day boundary conditions. We focus on springtime Arctic ozone minima and compare subsequent surface patterns in runs with and without interactive ozone, thus rendering a detailed and physically-based quantification of the stratospheric ozone impact on surface climate possible.  </p><p>All model simulations show a connection between Arctic ozone minima and a positive phase of the Arctic Oscillation in the month after the depletion in spring. Runs with interactive ozone chemistry show an amplified surface response and a 40% stronger Arctic Oscillation index after ozone depletion. This amplified Arctic Oscillation goes along with enhanced positive surface temperature anomalies over Eurasia. Moreover, composite surface patterns after spring ozone minima in model simulations with interactive ozone show a better agreement with composites in reanalysis data compared to runs with prescribed ozone.</p><p>Mechanisms whereby stratospheric ozone affects both the stratospheric and tropospheric circulation are explored. These include the reduction of short-wave heating over the pole due to ozone loss, thus amplifying stratospheric temperature anomalies and allowing for an intensification of the polar vortex with subsequent impacts on wave propagation and the stratospheric meridional circulation. This suggests that ozone is not only passively responding to stratospheric dynamics, but actively feeds back into the circulation. Following these results, stratospheric ozone anomalies actively contribute to anomalous surface weather in spring, emphasizing the potential importance of interactive ozone chemistry for seasonal predictions.</p>

The effects of ultraviolet-B radiation on freshwater ecosystems of the Arctic: Influence from stratospheric ozone depletion and climate change

2004 ◽  
Vol 12 (1) ◽  
pp. 1-70 ◽  
Author(s):  
S Perin ◽  
D RS Lean
Keyword(s):  
Climate Change ◽  
Uv Radiation ◽  
Climate Warming ◽  
Ozone Depletion ◽  
Aquatic Ecosystems ◽  
Stratospheric Ozone ◽  
Aquatic Organisms ◽  
Ultraviolet B ◽  
The Arctic ◽  
Uvb Radiation

Depletion of stratospheric ozone, the principal atmospheric attenuator of ultraviolet-B (UVB) radiation, by man-made chemicals has raised scientific and public concern regarding the biological effects of increased UVB radiation on Earth. There is an increased awareness that existing levels of solar UV radiation have an important influence on biological and chemical processes in aquatic ecosystems. For aquatic organisms, numerous studies have shown direct detrimental effects of UVB radiation at each trophic level. Fortunately, many aquatic organisms also possess a range of photoprotective mechanisms against UV radiation toxicity. In addition to its direct impact, harmful effects of UVB radiation at a single-trophic level can cascade through the food web and indirectly affect organisms from other trophic levels. Because UV radiation photochemically reacts with humic substances and other photosensitive agents in the water, increases in solar UVB can also indirectly affect aquatic organisms through the production and (or) release of different photoproducts like biologically available nutrients and harmful reactive oxygen species. Polar aquatic ecosystems have been of particular concern, since stratospheric ozone-related UVB increases have been the greatest in these regions. With the influences of climate warming and the possibility of future volcanic eruptions, ozone losses are expected to get worse in the Arctic stratosphere, and the ozone layer recovery may not follow the slow decline of industrial ozone-depleting compounds in the atmosphere. Climate warming is also expected to bring important changes in underwater ultraviolet radiation (UVR) penetration in Arctic freshwaters that would be more significant to the aquatic biota than stratospheric ozone depletion.Key words: Arctic, UV radiation, UVB, ozone depletion, climate change, aquatic ecosystems.

scholarly journals Possible Effects of Ozone Depletion on the Global Carbon Cycle

Radiocarbon ◽  
1992 ◽  
Vol 34 (3) ◽  
pp. 772-779 ◽  
Author(s):  
Tsung-Hung Peng
Keyword(s):  
Ozone Depletion ◽  
Stratospheric Ozone ◽  
Maximum Effect ◽  
Antarctic Ocean ◽  
Box Models ◽  
Marine Productivity ◽  
Business As Usual ◽  
The Antarctic ◽  
Global Oceans ◽  
Global Carbon

The increase of UV-B radiation resulting from ozone depletion is considered to have damaging effects on marine ecosystems. A cutback of marine productivity would tend to reduce the oceanic uptake of atmospheric CO2. Box models of the global oceans based on the distribution of bomb-produced 14C are used to evaluate the possible effects of ozone depletion on the atmospheric CO2 concentration. The maximum effect presumably takes place if the ozone hole reduces the marine productivity to zero in the Antarctic Ocean. In a business-as-usual scenario of future CO2 emissions, the atmospheric CO2 partial pressure (pCO2) would increase by an additional 37 μatm over the course of the next century. This increase corresponds to 4.6% of the projected atmospheric pCO2 in the year 2090. However, if the damaging effect caused by the destruction of the stratospheric ozone layer is assumed to lower the productivity over the Antarctic Ocean by 10%, the atmospheric pCO2 would rise by less than 3 μatm over the expected atmospheric level in the next century.

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