scholarly journals Montreal Protocol benefits simulated with CCM SOCOL

2012 ◽  
Vol 12 (7) ◽  
pp. 17001-17030 ◽  
Author(s):  
T. Egorova ◽  
E. Rozanov ◽  
J. Gröbner ◽  
M. Hauser ◽  
W. Schmutz

Abstract. Ozone depletion is caused by the anthropogenic increase of halogen containing species in the atmosphere, which results in the enhancement of the concentration of reactive chlorine and bromine in the stratosphere. To reduce the influence of anthropogenic ozone-depleting substances (ODS), the Montreal Protocol was agreed by Governments in 1987, with several Amendments adopted later. In order to assess the benefits of the Montreal Protocol and its Amendments (MPA) on ozone and UV radiation, two different runs of the chemistry-climate model (CCM) SOCOL have been carried out. The first run was driven by the emission of ozone depleting substances (ODS) prescribed according to the restrictions of the Montreal Protocol and all its Amendments. For the second run we allow the ODS to grow by 3% annually. We find that the MPA would have saved up to 80% of the global annual total ozone by the end of the 21st century. Our calculations also show substantial changes in surface temperature and precipitations that could occur in the world without MPA implementations. To illustrate the changes in UV radiation at the surface and to emphasize certain features which can only be seen for some particular regions if the influence of the cloud cover changes is accounted for, we calculate geographical distribution of the erythemally weighted irradiance (Eery). For the no Montreal Protocol simulation Eery increases by factor of 4 to 16 between the 1970s and 2100. For the scenario including the Montreal Protocol it is found that UV radiation starts to decrease in 2000, with continuous decline of 5% to 10% at middle latitudes in the Northern and Southern hemispheres.

2013 ◽  
Vol 13 (7) ◽  
pp. 3811-3823 ◽  
Author(s):  
T. Egorova ◽  
E. Rozanov ◽  
J. Gröbner ◽  
M. Hauser ◽  
W. Schmutz

Abstract. Ozone depletion is caused by the anthropogenic increase of halogen-containing species in the atmosphere, which results in the enhancement of the concentration of reactive chlorine and bromine in the stratosphere. To reduce the influence of anthropogenic ozone-depleting substances (ODS), the Montreal Protocol was agreed by Governments in 1987, with several Amendments and Adjustments adopted later. In order to assess the benefits of the Montreal Protocol and its Amendments and Adjustments (MPA) on ozone and UV radiation, two different runs of the chemistry-climate model (CCM) SOCOL have been carried out. The first run was driven by the emission of ozone depleting substances (ODS) prescribed according to the restrictions of the MPA. For the second run we allow the ODS to grow by 3% annually. We find that the MPA would have saved up to 80% of the global annual total ozone by the end of the 21st century. Our calculations also show substantial changes of the stratospheric circulation pattern as well as in surface temperature and precipitations that could occur in the world without MPA implementations. To illustrate the changes in UV radiation at the surface and to emphasise certain features, which can only be seen for some particular regions if the influence of the cloud cover changes is accounted for, we calculate geographical distribution of the erythemally weighted irradiance (Eery). For the no Montreal Protocol simulation Eery increases by factor of 4 to 16 between the 1970s and 2100. For the scenario including the Montreal Protocol it is found that UV radiation starts to decrease in 2000, with continuous decline of 5% to 10% at middle latitudes in the both Northern and Southern Hemispheres.


2022 ◽  
Author(s):  
Mark Weber ◽  
Carlo Arosio ◽  
Melanie Coldewey-Egbers ◽  
Vitali Fioletov ◽  
Stacey M. Frith ◽  
...  

Abstract. We report on updated trends using different merged zonal mean total ozone datasets from satellite and ground-based observations for the period from 1979 to 2020. This work is an update from the trends reported in Weber et al. (2018) using the same datasets up to 2016. Merged datasets used in this study include NASA MOD v8.7 and NOAA Cohesive Data (COH) v8.6, both based on data from the series of Solar Backscatter UltraViolet (SBUV), SBUV-2, and Ozone Mapping and Profiler Suite (OMPS) satellite instruments (1978–present) as well as the Global Ozone Monitoring Experiment (GOME)-type Total Ozone (GTO-ECV) and GOME-SCIAMACHY-GOME-2 (GSG) merged datasets (both 1995–present), mainly comprising satellite data from GOME, SCIAMACHY, OMI, GOME-2A, -2B, and TROPOMI. The fifth dataset consists of the annual mean zonal mean data from ground-based measurements collected at the World Ozone and UV Radiation Data Center (WOUDC). Trends were determined by applying a multiple linear regression (MLR) to annual mean zonal mean data. The addition of four more years consolidated the fact that total ozone is indeed on slowly recovering in both hemispheres as a result of phasing out ozone depleting substances (ODS) as mandated by the Montreal Protocol. The near global ozone trend of the median of all datasets after 1996 was 0.5 ± 0.2 (2σ) %/decade, which is in absolute numbers roughly a third of the decreasing rate of 1.4 ± 0.6 %/decade from 1978 until 1996. The ratio of decline and increase is nearly identical to that of the EESC (equivalent effective stratospheric chlorine or stratospheric halogen) change rates before and after 1996 which confirms the success of the Montreal Protocol. The observed trends are also in very good agreement with the median of 17 chemistry climate models from CCMI (Chemistry Climate Model Initiative) with current ODS and GHG (greenhouse gas) scenarios. The positive ODS related trends in the NH after 1996 are only obtained with a sufficient number of terms in the MLR accounting properly for dynamical ozone changes (Brewer-Dobson circulation, AO, AAO). A standard MLR (limited to solar, QBO, volcanic, and ENSO) leads to zero trends showing that the small positive ODS related trends have been balanced by negative trend contributions from atmospheric dynamics resulting in nearly constant total ozone levels since 2000.


2013 ◽  
Vol 26 (12) ◽  
pp. 4049-4068 ◽  
Author(s):  
Yutian Wu ◽  
Lorenzo M. Polvani ◽  
Richard Seager

Abstract The 1987 Montreal Protocol regulating emissions of chlorofluorocarbons (CFCs) and other ozone-depleting substances (ODSs) was motivated primarily by the harm to human health and ecosystems arising from increased exposure to ultraviolet-B (UV-B) radiation associated with depletion of the ozone layer. It is now known that the Montreal Protocol has helped reduce radiative forcing of the climate system since CFCs are greenhouse gases (GHGs), and that ozone depletion (which is now on the verge of reversing) has been the dominant driver of atmospheric circulation changes in the Southern Hemisphere in the last half century. This paper demonstrates that the Montreal Protocol also significantly protects Earth’s hydroclimate. Using the Community Atmospheric Model, version 3 (CAM3), coupled to a simple mixed layer ocean, it is shown that in the “world avoided” (i.e., with CFC emissions not regulated), the subtropical dry zones would be substantially drier, and the middle- and high-latitude regions considerably wetter in the coming decade (2020–29) than in a world without ozone depletion. Surprisingly, these changes are very similar, in both pattern and magnitude, to those caused by projected increases in GHG concentrations over the same period. It is further shown that, by dynamical and thermodynamical mechanisms, both the stratospheric ozone depletion and increased CFCs contribute to these changes. The results herein imply that, as a consequence of the Montreal Protocol, changes in the hydrological cycle in the coming decade will be only half as strong as what they otherwise would be.


2016 ◽  
Vol 29 (6) ◽  
pp. 2275-2289 ◽  
Author(s):  
Lorenzo M. Polvani ◽  
Suzana J. Camargo ◽  
Rolando R. Garcia

Abstract The impact of the Montreal Protocol on the potential intensity of tropical cyclones over the next 50 years is investigated with the Whole Atmosphere Community Climate Model (WACCM), a state-of-the-art, stratosphere-resolving atmospheric model, coupled to land, ocean, and sea ice components, with interactive stratospheric chemistry. An ensemble of WACCM runs from 2006 to 2065 forced with a standard future scenario is compared to a second ensemble in which ozone-depleting substances (ODS) are not regulated (the so-called World Avoided). It is found that by the year 2065, changes in the potential intensity of tropical cyclones in the World Avoided are nearly 3 times as large as for the standard scenario. The Montreal Protocol thus provides a strong mitigation of the adverse effects of intensifying tropical cyclones. The relative importance of warmer sea surface temperatures (ozone-depleting substances are important greenhouse gases) and cooler lower-stratospheric temperatures (accompanying the massive destruction of the ozone layer) is carefully examined. It is found that the former are largely responsible for the increase in potential intensity in the World Avoided, whereas temperatures above the 70-hPa level—which plunge by nearly 15 K in 2065 in the World Avoided—have no discernible effect on potential intensity. This finding suggests that the modest (compared to the World Avoided) tropical ozone depletion of recent decades has not been a major player in determining the intensity of tropical cyclones, and neither will ozone recovery be in the coming half century.


Author(s):  
A. S. Pastukhova ◽  
N. E. Chubarova ◽  
Ye. Yu. Zhdanova ◽  
V. Ya. Galin ◽  
S. P. Smyshlyaev

In this work, the impact of various factors on the total ozone column and erythemal UV radiation (Qery) in the territory of Northern Eurasia for the period from 1979 to 2059 based on the calculations of the chemical-climate model INM-RHSU is analyzed. The sensitivity of ozone recovery to the setting of different input data on sea surface temperature (SST) is estimated. Depending on the SST datasets, there are significant differences in ozone trends. A possible mechanism that explains the reasons for these differences is examined. The numerical experiment with the only change in ozone depleting substances according to Montreal protocol showed the ozone recovery and, as a result, Qery reduction, but this recovery is not linear. During the 2016-2020 period we estimated the 2-5% increase in Qery values relative to the baseline period (1979-1983) with about 6% maximum over Russian polar region. During the 2035-2039 period the Qery change against 1979-1983 period is about zero, during the 2055-2059 period we obtained the decrease of about 4-6% over Northern Asia and 6-8% over Northern Europe These changes corresponded to the noticeable boundary location shift of UV resources, which determine UV radiation impact on human health. The most significant changes will be observed in spring and summer: the UV deficiency zone will be expanded in the north and the UV excess zone over northern seas will be reduced in the south.


2021 ◽  
Author(s):  
Ewa Bednarz ◽  
Ryan Hossaini ◽  
Luke Abraham ◽  
Peter Braesicke ◽  
Martyn Chipperfield

<p>The emissions of most long-lived halogenated ozone-depleting substances (ODSs) are now decreasing, owing to controls on their production introduced by Montreal Protocol and its amendments. However, short-lived halogenated compounds can also have substantial impact on atmospheric chemistry, including stratospheric ozone, particularly if emitted near climatological uplift regions. It has recently become evident that emissions of some chlorinated very short-lived species (VSLSs), such as chloroform (CHCl<sub>3</sub>) and dichloromethane (CH<sub>2</sub>Cl<sub>2</sub>), could be larger than previously believed and increasing, particularly in Asia. While these may exert a significant influence on atmospheric chemistry and climate, their impacts remain poorly characterised. </p><p> </p><p>We address this issue using the UM-UKCA chemistry-climate model (CCM). While not only the first, to our knowledge, model study addressing this problem using a CCM, it is also the first such study employing a whole atmosphere model, thereby simulating the tropospheric Cl-VSLSs emissions and the resulting stratospheric impacts in a fully consistent manner. We use a newly developed Double-Extended Stratospheric-Tropospheric (DEST) chemistry scheme, which includes emissions of all major chlorinated and brominated VSLSs alongside an extended treatment of long-lived ODSs.</p><p> </p><p>We examine the impacts of rising Cl-VSLSs emissions on atmospheric chlorine tracers and ozone, including their long-term trends. We pay particular attention to the role of ‘nudging’, as opposed to the free-running model set up, for the simulated Cl-VSLSs impacts, thereby demostrating the role of atmospheric dynamics in modulating the atmospheric responses to Cl-VSLSs. In addition, we employ novel estimates of Cl-VSLS emissions over the recent past and compare the results with the simulations that prescribe Cl-VSLSs using simple lower boundary conditions. This allows us to demonstrate the impact such choice has on the dominant location and seasonality of the Cl-VSLSs transport into the stratosphere.</p>


2019 ◽  
Vol 19 (19) ◽  
pp. 12309-12324 ◽  
Author(s):  
Maxime Prignon ◽  
Simon Chabrillat ◽  
Daniele Minganti ◽  
Simon O'Doherty ◽  
Christian Servais ◽  
...  

Abstract. Hydrochlorofluorocarbons (HCFCs) are the first, but temporary, substitution products for the strong ozone-depleting chlorofluorocarbons (CFCs). HCFC consumption and production are currently regulated under the Montreal Protocol on Substances that Deplete the Ozone Layer and their emissions have started to stabilize or even decrease. As HCFC-22 (CHClF2) is by far the most abundant HCFC in today's atmosphere, it is crucial to continue to monitor the evolution of its atmospheric concentration. In this study, we describe an improved HCFC-22 retrieval strategy from ground-based high-resolution Fourier transform infrared (FTIR) solar spectra recorded at the high-altitude scientific station of Jungfraujoch, the Swiss Alps, 3580 m a.m.s.l. (above mean sea level). This new strategy distinguishes tropospheric and lower-stratospheric partial columns. Comparisons with independent datasets, such as the Advanced Global Atmospheric Gases Experiment (AGAGE) and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS), supported by models, such as the Belgian Assimilation System for Chemical ObErvation (BASCOE) and the Whole Atmosphere Community Climate Model (WACCM), demonstrate the validity of our tropospheric and lower-stratospheric long-term time series. A trend analysis on the datasets used here, now spanning 30 years, confirms the last decade's decline in the HCFC-22 growth rate. This updated retrieval strategy can be adapted for other ozone-depleting substances (ODSs), such as CFC-12. Measuring or retrieving ODS atmospheric concentrations is essential for scrutinizing the fulfilment of the globally ratified Montreal Protocol.


2010 ◽  
Vol 10 (16) ◽  
pp. 7697-7707 ◽  
Author(s):  
J. S. Daniel ◽  
E. L. Fleming ◽  
R. W. Portmann ◽  
G. J. M. Velders ◽  
C. H. Jackman ◽  
...  

Abstract. Hypothetical reductions in future emissions of ozone-depleting substances (ODSs) and N2O are evaluated in terms of effects on equivalent effective stratospheric chlorine (EESC), globally-averaged total column ozone, and radiative forcing through 2100. Due to the established success of the Montreal Protocol, these actions can have only a fraction of the impact on ozone depletion that regulations already in force have had. If all anthropogenic ODS and N2O emissions were halted beginning in 2011, ozone is calculated to be higher by about 1–2% during the period 2030–2100 compared to a case of no additional restrictions. Direct radiative forcing by 2100 would be about 0.23 W/m2 lower from the elimination of anthropogenic N2O emissions and about 0.005 W/m2 lower from the destruction of the chlorofluorocarbon (CFC) bank. Due to the potential impact of N2O on future ozone levels, we provide an approach to incorporate it into the EESC formulation, which is used extensively in ozone depletion analyses. The ability of EESC to describe total ozone changes arising from additional ODS and N2O controls is also quantified.


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.


2012 ◽  
Vol 4 (1) ◽  
pp. 91-100 ◽  
Author(s):  
K. Vaníček ◽  
L. Metelka ◽  
P. Skřivánková ◽  
M. Staněk

Abstract. Homogenized data series of total ozone measurements taken by the regularly and well calibrated Dobson and Brewer spectrophotometers at Hradec Králové (Czech) and the data from the re-analyses ERA-40 and ERA-Interim were merged and compared to investigate differences between the particular data sets originated in Central Europe, the Northern Hemisphere (NH) mid-latitudes. The Dobson-to-Brewer transfer function and the algorithm for approximation of the data from the re-analyses were developed, tested and applied for creation of instrumentally consistent and completed total ozone data series of the 50-yr period 1961–2010 of observations. This correction has reduced the well-known seasonal differences between Dobson and Brewer data below the 1% calibration limit of the spectrophotometers. Incorporation of the ERA-40 and ERA-Interim total ozone data on days with missing measurements significantly improved completeness and reliability of the data series mainly in the first two decades of the period concerned. Consistent behaviour of the original and corrected/merged data sets was found in the pre-ozone-hole period (1961–1985). In the post-Pinatubo (1994–2010) era the data series show seasonal differences that can introduce uncertainty in estimation of ozone recovery mainly in the winter-spring season when the effect of the Montreal Protocol and its Amendments is expected. All the data sets confirm substantial depletion of ozone also in the summer months that gives rise to the question about its origin. The merged and completed data series of total ozone will be further analyzed to quantify chemical ozone losses and contribution of natural atmospheric processes to the ozone depletion over the region. This case study points out the importance of selection and evaluation of the quality and consistency of the input data sets used in estimation of long-term ozone changes including recovery of the ozone layer over the selected areas. Data are available from the PANGAEA database at doi:10.1594/PANGAEA.779819.


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