scholarly journals The Importance of the Montreal Protocol in Mitigating the Potential Intensity of Tropical Cyclones

2016 ◽  
Vol 29 (6) ◽  
pp. 2275-2289 ◽  
Author(s):  
Lorenzo M. Polvani ◽  
Suzana J. Camargo ◽  
Rolando R. Garcia
Keyword(s):  
Tropical Cyclones ◽  
Climate Model ◽  
Atmospheric Model ◽  
Montreal Protocol ◽  
Discernible Effect ◽  
Major Player ◽  
The World ◽  
Standard Scenario ◽  
Ozone Depleting Substances ◽  
The Impact

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.

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>

Improved characterisation of the impact of chlorinated VSLSs on atmospheric chemistry and climate: past, present and future

2020 ◽  
Author(s):  
Ewa Bednarz ◽  
Ryan Hossaini ◽  
Luke Abraham ◽  
Martyn Chipperfield
Keyword(s):  
Atmospheric Chemistry ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Montreal Protocol ◽  
Recent Past ◽  
Substantial Impact ◽  
Emissions Scenarios ◽  
Ozone Depleting Substances ◽  
The Impact ◽  
Future Emissions

<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. 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. Employing novel estimates of Cl-VSLS emissions we show model results regarding the atmospheric impacts of chlorinated VSLSs over the recent past (2000-present), with a focus on stratospheric ozone and HCl trends. Finally, we introduce our plans regarding examining the impacts of chlorinated VSLSs under a range of potential future emissions scenarios; the results of which will be directly relevant for the next WMO/UNEP assessment.</p>

scholarly journals The Importance of the Montreal Protocol in Protecting Earth’s Hydroclimate

2013 ◽  
Vol 26 (12) ◽  
pp. 4049-4068 ◽  
Author(s):  
Yutian Wu ◽  
Lorenzo M. Polvani ◽  
Richard Seager
Keyword(s):  
Ozone Depletion ◽  
Radiative Forcing ◽  
Hydrological Cycle ◽  
Stratospheric Ozone ◽  
Atmospheric Model ◽  
Ultraviolet B ◽  
Montreal Protocol ◽  
Mixed Layer Ocean ◽  
The World ◽  
Ozone Depleting Substances

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.

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.

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 Changing trends and emissions of hydrochlorofluorocarbons and their hydrofluorocarbon replacements

2016 ◽  
Author(s):  
Peter G. Simmonds ◽  
Matthew Rigby ◽  
Archibold McCulloch ◽  
Simon O'Doherty ◽  
Dickon Young ◽  
...  
Keyword(s):  
Growth Rates ◽  
Montreal Protocol ◽  
Hfc 134A ◽  
Production And Consumption ◽  
Ozone Depleting Substances ◽  
Phase Out ◽  
Article 5 ◽  
The Impact ◽  
Global Emissions

Abstract. High frequency, in situ global observations of HCFC-22 (CHClF2), HCFC-141b (CH3CCl2F), HCFC-142b (CH3CClF2) and HCFC-124 (CHClFCF3) and their main HFC replacements HFC-134a (CH2FCF3), HFC-125 (CHF2CF3), HFC-143a (CH3CF3), and HFC-32 (CH2F2) have been used to determine their changing global growth rates and emissions in response to the Montreal Protocol and its recent amendments. The 2007 adjustment to the Montreal Protocol required the accelerated phase-out of HCFCs with global production and consumption capped in 2013, to mitigate their environmental impact as both ozone depleting substances and important greenhouse gases. We find that this change has coincided with a reduction in global emissions of the four HCFCs with aggregated global emissions in 2015 of 444 ± 75 Gg/yr, in CO2 equivalent units (CO2 e) 0.75 ± 0.1 Gt/yr, compared with 483 ± 70 Gg/yr (0.82 ± 0.1 Gt/yr CO2 e) in 2010. (All quoted uncertainties in this paper are 1 sigma). About 80 % of the total HCFC atmospheric burden in 2015 is HCFC-22, where global HCFC emissions appear to have been relatively constant in spite of the 2013 cap on global production and consumption. We attribute this to a probable increase in production and consumption of HCFC-22 in Montreal Protocol Article 5 (developing) countries and the continuing release of HCFC-22 from the large banks which dominate HCFC global emissions. Conversely, the four HFCs all show increasing annual growth rates with aggregated global HFCs emissions in 2015 of 329 ± 70 Gg/yr (0.65 ± 0.12 Gt/yr CO2 e) compared to 2010 with 240 ± 50 Gg/yr (0.47 ± 0.08 Gt/yr CO2 e). As HCFCs are replaced by HFCs we investigate the impact of the shift to refrigerant blends which have lower global warming potentials (GWPs). We also note that emissions of HFC-125 and HFC-32 appear to have increased more rapidly during the 2011–2015 5-yr period compared to 2006–2010.

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.

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.

Dust Aerosol Important for Snowball Earth Deglaciation

2010 ◽  
Vol 23 (15) ◽  
pp. 4121-4132 ◽  
Author(s):  
Dorian S. Abbot ◽  
Itay Halevy
Keyword(s):  
Climate Models ◽  
Climate Model ◽  
Global Climate ◽  
Global Climate Model ◽  
Atmospheric Model ◽  
Dust Aerosol ◽  
Snowball Earth ◽  
Dust Aerosols ◽  
Co2 Levels ◽  
The Impact

Abstract Most previous global climate model simulations could only produce the termination of Snowball Earth episodes at CO2 partial pressures of several tenths of a bar, which is roughly an order of magnitude higher than recent estimates of CO2 levels during and shortly after Snowball events. These simulations have neglected the impact of dust aerosols on radiative transfer, which is an assumption of potentially grave importance. In this paper it is argued, using the Dust Entrainment and Deposition (DEAD) box model driven by GCM results, that atmospheric dust aerosol concentrations may have been one to two orders of magnitude higher during a Snowball Earth event than today. It is furthermore asserted on the basis of calculations using NCAR’s Single Column Atmospheric Model (SCAM)—a radiative–convective model with sophisticated aerosol, cloud, and radiative parameterizations—that when the surface albedo is high, such increases in dust aerosol loading can produce several times more surface warming than an increase in the partial pressure of CO2 from 10−4 to 10−1 bar. Therefore the conclusion is reached that including dust aerosols in simulations may reconcile the CO2 levels required for Snowball termination in climate models with observations.

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