scholarly journals Montreal Protocol Benefits simulated with CCM SOCOL

2013 ◽  
Vol 13 (7) ◽  
pp. 3811-3823 ◽  
Author(s):  
T. Egorova ◽  
E. Rozanov ◽  
J. Gröbner ◽  
M. Hauser ◽  
W. Schmutz
Keyword(s):  
Uv Radiation ◽  
Ozone Depletion ◽  
Climate Model ◽  
Circulation Pattern ◽  
Montreal Protocol ◽  
Middle Latitudes ◽  
Annual Total ◽  
Stratospheric Circulation ◽  
Ozone Depleting Substances ◽  
Northern And Southern Hemispheres

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.

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
Keyword(s):  
Uv Radiation ◽  
Ozone Depletion ◽  
Total Ozone ◽  
Climate Model ◽  
Montreal Protocol ◽  
Middle Latitudes ◽  
The World ◽  
Annual Total ◽  
Ozone Depleting Substances ◽  
Northern And Southern Hemispheres

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.

scholarly journals The forecast of erythemal UV irradiance over the territory of Northern Eurasia according to the INM-RSHU chemical-climate model

2019 ◽  
Vol 55 (3) ◽  
pp. 20-28
Author(s):  
A. S. Pastukhova ◽  
N. E. Chubarova ◽  
Ye. Yu. Zhdanova ◽  
V. Ya. Galin ◽  
S. P. Smyshlyaev
Keyword(s):  
Uv Radiation ◽  
Climate Model ◽  
Baseline Period ◽  
Montreal Protocol ◽  
Northern Eurasia ◽  
Northern Asia ◽  
The North ◽  
Chemical Climate ◽  
Ozone Depleting Substances ◽  
The Impact

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.

Atmospheric impacts of short-lived chlorinated species over the recent past: a chemistry-climate perspective

2021 ◽  
Author(s):  
Ewa Bednarz ◽  
Ryan Hossaini ◽  
Luke Abraham ◽  
Peter Braesicke ◽  
Martyn Chipperfield
Keyword(s):  
Atmospheric Chemistry ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Lower Boundary ◽  
Montreal Protocol ◽  
Recent Past ◽  
Substantial Impact ◽  
Ozone Depleting Substances ◽  
The Impact

<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>

scholarly journals Improved FTIR retrieval strategy for HCFC-22 (CHClF<sub>2</sub>), comparisons with in situ and satellite datasets with the support of models, and determination of its long-term trend above Jungfraujoch

2019 ◽  
Vol 19 (19) ◽  
pp. 12309-12324 ◽  
Author(s):  
Maxime Prignon ◽  
Simon Chabrillat ◽  
Daniele Minganti ◽  
Simon O'Doherty ◽  
Christian Servais ◽  
...  
Keyword(s):  
Climate Model ◽  
Michelson Interferometer ◽  
Montreal Protocol ◽  
Swiss Alps ◽  
Retrieval Strategy ◽  
Atmospheric Concentration ◽  
New Strategy ◽  
Scientific Station ◽  
Ozone Depleting Substances

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.

scholarly journals Options to accelerate ozone recovery: ozone and climate benefits

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 ◽  
...  
Keyword(s):  
Ozone Depletion ◽  
Radiative Forcing ◽  
Montreal Protocol ◽  
N2o Emissions ◽  
Total Column Ozone ◽  
Potential Impact ◽  
Ozone Depleting Substances ◽  
Column Ozone ◽  
The Impact ◽  
Total Column

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.

scholarly journals Antarctic ozone depletion between 1960 and 1980 in observations and chemistry–climate model simulations

2016 ◽  
Vol 16 (24) ◽  
pp. 15619-15627 ◽  
Author(s):  
Ulrike Langematz ◽  
Franziska Schmidt ◽  
Markus Kunze ◽  
Gregory E. Bodeker ◽  
Peter Braesicke
Keyword(s):  
Ozone Depletion ◽  
Climate Model ◽  
Total Column Ozone ◽  
Antarctic Ozone ◽  
Climate Model Simulations ◽  
Ozone Depleting Substances ◽  
Column Ozone ◽  
The Antarctic ◽  
Total Column

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.

scholarly journals Stronger Arctic amplification from ozone-depleting substances than from carbon dioxide

2022 ◽  
Author(s):  
Yu-Chiao Liang ◽  
Lorenzo M. Polvani ◽  
Michael Previdi ◽  
Karen Louise Smith ◽  
Mark R. England ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Sea Ice ◽  
Climate Model ◽  
Montreal Protocol ◽  
Lapse Rate ◽  
The Arctic ◽  
Arctic Amplification ◽  
Near Surface ◽  
Arctic Warming ◽  
Ozone Depleting Substances

Abstract Arctic amplification (AA) - the greater warming of the Arctic near-surface temperature relative to its global mean value - is a prominent feature of the climate response to increasing greenhouse gases. Recent work has revealed the importance of ozone-depleting substances (ODS) in contributing to Arctic warming and sea-ice loss. Here, using ensembles of climate model integrations, we expand on that work and directly contrast Arctic warming from ODS to that from carbon dioxide (CO$_2$), over the 1955-2005 period when ODS loading peaked. We find that the Arctic warming and sea-ice loss from ODS are slightly more than half (52-59\%) those from CO$_2$. We further show that the strength of AA for ODS is 1.44 times larger than that for CO$_2$, and that this mainly stems from more positive Planck, albedo, lapse-rate, and cloud feedbacks. Our results suggest that AA would be considerably stronger than presently observed had the Montreal Protocol not been signed.

scholarly journals Global total ozone recovery trends derived from five merged ozone datasets

2022 ◽  
Author(s):  
Mark Weber ◽  
Carlo Arosio ◽  
Melanie Coldewey-Egbers ◽  
Vitali Fioletov ◽  
Stacey M. Frith ◽  
...  
Keyword(s):  
Data Center ◽  
Total Ozone ◽  
Climate Models ◽  
Climate Model ◽  
Montreal Protocol ◽  
Before And After ◽  
Ozone Trend ◽  
Ozone Monitoring ◽  
Ozone Depleting Substances ◽  
Good Agreement

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.

Global Impact of the CFC Phaseout

1991 ◽  
Vol 34 (3) ◽  
pp. 17-22
Author(s):  
Stephen Andersen
Keyword(s):  
Ozone Depletion ◽  
Chemical Compounds ◽  
Cost Effective ◽  
Clean Air Act ◽  
Scientific Data ◽  
Montreal Protocol ◽  
Methyl Chloroform ◽  
Clean Air ◽  
Environmentally Sound ◽  
Ozone Depleting Substances

The amendments to the Montreal Protocol and the 1990 Clean Air Act call for the accelerated reduction of fully halogenated CFCs and halons. Recent scientific data indicate that these chemicals are more damaging to the earth's ozone layer than previously thought. This ozone depletion has serious consequences for the environment and human health. These chemical compounds are scheduled for phaseout under the Montreal Protocol and Clean Air Act. Because CFC-13 and methyl chloroform are used extensively in the electronics industry worldwide, the industry and the U.S. EPA have formed a partnership to develop technically feasible, cost-effective, and environmentally sound alternatives for ozone-depleting substances.

Emergence of Southern Hemisphere circulation changes in response to ozone recovery

2020 ◽  
Author(s):  
Brian Zambri ◽  
Susan Solomon ◽  
David Thompson ◽  
Qiang Fu
Keyword(s):  
Southern Hemisphere ◽  
Ozone Depletion ◽  
Stratospheric Ozone ◽  
Polar Vortex ◽  
Montreal Protocol ◽  
Stratospheric Polar Vortex ◽  
Surface Climate ◽  
Antarctic Ozone ◽  
Ozone Depleting Substances ◽  
Circulation Changes

&lt;p&gt;Ozone depletion in the Southern Hemisphere (SH) stratosphere in the late 20&lt;sup&gt;th&lt;/sup&gt; century cooled the air there, strengthening the SH stratospheric westerly winds near 60&amp;#186;S and altering SH surface climate. Since ~1999, trends in Antarctic ozone have begun to recover, exhibiting a flattening followed by a sign reversal in response to decreases in stratospheric chlorine concentration due to the Montreal Protocol, an international treaty banning the production and consumption of ozone-depleting substances. Here we show that the post&amp;#8211;1999 increase in ozone has resulted in thermal and circulation changes of opposite sign to those that resulted from stratospheric ozone losses, including a warming of the SH polar lower stratosphere and a weakening of the SH stratospheric polar vortex.&amp;#160; Further, these altered trends extend to the upper troposphere, albeit of smaller magnitudes. &amp;#160;Observed post&amp;#8211;1999 trends of temperature and circulation in the stratosphere are about 20&amp;#8211;25% the magnitude of those of the ozone depletion era, and are broadly consistent with expectations based on modeled depletion-era trends and variability of both ozone and reactive chlorine, thereby indicating the emergence of healing of dynamical impacts of the Antarctic ozone hole.&lt;/p&gt;

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