Quantifying the Summertime Response of the Austral Jet Stream and Hadley Cell to Stratospheric Ozone and Greenhouse Gases

2014 ◽  
Vol 27 (14) ◽  
pp. 5538-5559 ◽  
Author(s):  
Edwin P. Gerber ◽  
Seok-Woo Son
Keyword(s):  
Greenhouse Gases ◽  
Climate Sensitivity ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Coupled Model ◽  
Hadley Cell ◽  
Dynamical Response ◽  
Jet Stream ◽  
Temperature Trends ◽  
The Impact

Abstract The impact of anthropogenic forcing on the summertime austral circulation is assessed across three climate model datasets: the Chemistry–Climate Model Validation activity 2 and phases 3 and 5 of the Coupled Model Intercomparison Project. Changes in stratospheric ozone and greenhouse gases impact the Southern Hemisphere in this season, and a simple framework based on temperature trends in the lower polar stratosphere and upper tropical troposphere is developed to separate their effects. It suggests that shifts in the jet stream and Hadley cell are driven by changes in the upper-troposphere–lower-stratosphere temperature gradient. The mean response is comparable in the three datasets; ozone has chiefly caused the poleward shift observed in recent decades, while ozone and greenhouse gases largely offset each other in the future. The multimodel mean perspective, however, masks considerable spread in individual models’ circulation projections. Spread resulting from differences in temperature trends is separated from differences in the circulation response to a given temperature change; both contribute equally to uncertainty in future circulation trends. Spread in temperature trends is most associated with differences in polar stratospheric temperatures, and could be narrowed by reducing uncertainty in future ozone changes. Differences in tropical temperatures are also important, and arise from both uncertainty in future emissions and differences in models’ climate sensitivity. Differences in climate sensitivity, however, only matter significantly in a high emissions future. Even if temperature trends were known, however, differences in the dynamical response to temperature changes must be addressed to substantially narrow spread in circulation projections.

scholarly journals Constraining Future Summer Austral Jet Stream Positions in the CMIP5 Ensemble by Process-Oriented Multiple Diagnostic Regression*

2016 ◽  
Vol 29 (2) ◽  
pp. 673-687 ◽  
Author(s):  
Sabrina Wenzel ◽  
Veronika Eyring ◽  
Edwin P. Gerber ◽  
Alexey Yu. Karpechko
Keyword(s):  
Stratospheric Ozone ◽  
Coupled Model ◽  
Jet Stream ◽  
Rcp Scenarios ◽  
Future Projections ◽  
Stratospheric Temperature ◽  
Temperature Trends ◽  
Wide Range ◽  
Ensemble Mean ◽  
Process Oriented

Abstract Stratospheric ozone recovery and increasing greenhouse gases are anticipated to have a large impact on the Southern Hemisphere extratropical circulation, shifting the jet stream and associated storm tracks. Models participating in phase 5 of the Coupled Model Intercomparison Project poorly simulate the austral jet, with a mean equatorward bias and 10° latitude spread in their historical climatologies, and project a wide range of future trends in response to anthropogenic forcing in the representative concentration pathway (RCP) scenarios. Here, the question is addressed whether the unweighted multimodel mean (uMMM) austral jet projection of the RCP4.5 scenario can be improved by applying a process-oriented multiple diagnostic ensemble regression (MDER). MDER links future projections of the jet position to processes relevant to its simulation under present-day conditions. MDER is first targeted to constrain near-term (2015–34) projections of the austral jet position and selects the historical jet position as the most important of 20 diagnostics. The method essentially recognizes the equatorward bias in the past jet position and provides a bias correction of about 1.5° latitude southward to future projections. When the target horizon is extended to midcentury (2040–59), the method also recognizes that lower-stratospheric temperature trends over Antarctica, a proxy for the intensity of ozone depletion, provide additional information that can be used to reduce uncertainty in the ensemble mean projection. MDER does not substantially alter the uMMM long-term position in jet position but reduces the uncertainty in the ensemble mean projection. This result suggests that accurate observational constraints on upper-tropospheric and lower-stratospheric temperature trends are needed to constrain projections of the austral jet position.

scholarly journals The impact of volcanic aerosols on stratospheric ozone and the Northern Hemisphere polar vortex: separating radiative from chemical effects under different climate conditions

2015 ◽  
Vol 15 (10) ◽  
pp. 14275-14314 ◽  
Author(s):  
S. Muthers ◽  
F. Arfeuille ◽  
C. C. Raible ◽  
E. Rozanov
Keyword(s):  
Northern Hemisphere ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Polar Vortex ◽  
Volcanic Eruptions ◽  
Radiative Heating ◽  
Dynamical Response ◽  
Climate Conditions ◽  
Column Ozone ◽  
The Impact

Abstract. After strong volcanic eruptions stratospheric ozone changes are modulated by heterogeneous chemical reactions (HET) and dynamical perturbations related to the radiative heating in the lower stratosphere (RAD). Here, we assess the relative importance of both processes as well as the effect of the resulting ozone changes on the dynamics using ensemble simulations with the atmosphere–ocean–chemistry–climate model (AOCCM) SOCOL-MPIOM forced by eruptions with different strength. The simulations are performed under present day and preindustrial conditions to investigate changes in the response behaviour. The results show that the HET effect is only relevant under present day conditions and causes a pronounced global reduction of column ozone. These ozone changes further lead to a slight weakening of the Northern Hemisphere (NH) polar vortex during mid-winter. Independent from the climate state the RAD mechanism changes the column ozone pattern with negative anomalies in the tropics and positive anomalies in the mid-latitudes. The influence of the climate state on the RAD mechanism significantly differs in the polar latitudes, where an amplified ozone depletion during the winter months is simulated under present day conditions. This is in contrast to the preindustrial state showing a positive column ozone response also in the polar area. The dynamical response of the stratosphere is clearly dominated by the RAD mechanism showing an intensification of the NH polar vortex in winter. Still under present day conditions ozone changes due to the RAD mechanism slightly reduce the response of the polar vortex after the eruption.

scholarly journals Stratospheric lifetime ratio of CFC-11 and CFC-12 from satellite and model climatologies

2014 ◽  
Vol 14 (11) ◽  
pp. 16865-16906 ◽  
Author(s):  
L. Hoffmann ◽  
C. M. Hoppe ◽  
R. Müller ◽  
G. S. Dutton ◽  
J. C. Gille ◽  
...  
Keyword(s):  
Global Warming ◽  
Atmospheric Chemistry ◽  
Climate Model ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Michelson Interferometer ◽  
Coupled Model ◽  
Model System ◽  
Satellite Observations ◽  
The Impact

Abstract. Chlorofluorocarbons (CFCs) play a key role in stratospheric ozone loss and are strong infrared absorbers that contribute to global warming. The stratospheric lifetimes of CFCs are a measure of their global loss rates that are needed to determine global warming and ozone depletion potentials. We applied the tracer-tracer correlation approach to zonal mean climatologies from satellite measurements and model data to assess the lifetimes of CFCl3 (CFC-11) and CF2Cl2 (CFC-12). We present estimates of the CFC-11/CFC-12 lifetime ratio and the absolute lifetime of CFC-12, based on a reference lifetime of 52 yr for CFC-11. We analyzed climatologies from three satellite missions, the Atmospheric Chemistry Experiment-Fourier Transform Spectrometer (ACE-FTS), the HIgh Resolution Dynamics Limb Sounder (HIRDLS), and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS). We found a CFC-11/CFC-12 lifetime ratio of 0.47±0.08 and a CFC-12 lifetime of 111(96–132) yr for ACE-FTS, a ratio of 0.46±0.07 and a lifetime of 112(97–133) yr for HIRDLS, and a ratio of 0.46±0.08 and a lifetime of 112(96–135) yr for MIPAS. The error-weighted, combined CFC-11/CFC-12 lifetime ratio is 0.47±0.04 and the CFC-12 lifetime estimate is 112(102–123) yr. These results agree with the recent Stratosphere-troposphere Processes And their Role in Climate (SPARC) reassessment, which recommends lifetimes of 52(43–67) yr and 102(88–122) yr, respectively. Having smaller uncertainties than the results from other recent studies, our estimates can help to better constrain CFC-11 and CFC-12 lifetime recommendations in future scientific studies and assessments. Furthermore, the satellite observations were used to validate first simulation results from a new coupled model system, which integrates a Lagrangian chemistry transport model into a climate model. For the coupled model we found a CFC-11/CFC-12 lifetime ratio of 0.48±0.07 and a CFC-12 lifetime of 110(95–129) yr, based on a ten-year perpetual run. Closely reproducing the satellite observations, the new model system will likely become a useful tool to assess the impact of advective transport, mixing, and photochemistry as well as climatological variability on the stratospheric lifetimes of long-lived tracers.

scholarly journals Stratospheric lifetime ratio of CFC-11 and CFC-12 from satellite and model climatologies

2014 ◽  
Vol 14 (22) ◽  
pp. 12479-12497 ◽  
Author(s):  
L. Hoffmann ◽  
C. M. Hoppe ◽  
R. Müller ◽  
G. S. Dutton ◽  
J. C. Gille ◽  
...  
Keyword(s):  
Global Warming ◽  
Atmospheric Chemistry ◽  
Climate Model ◽  
Transport Model ◽  
Stratospheric Ozone ◽  
Michelson Interferometer ◽  
Coupled Model ◽  
Model System ◽  
Satellite Observations ◽  
The Impact

Abstract. Chlorofluorocarbons (CFCs) play a key role in stratospheric ozone loss and are strong infrared absorbers that contribute to global warming. The stratospheric lifetimes of CFCs are a measure of their stratospheric loss rates that are needed to determine global warming and ozone depletion potentials. We applied the tracer–tracer correlation approach to zonal mean climatologies from satellite measurements and model data to assess the lifetimes of CFCl3 (CFC-11) and CF2Cl2 (CFC-12). We present estimates of the CFC-11/CFC-12 lifetime ratio and the absolute lifetime of CFC-12, based on a reference lifetime of 52 years for CFC-11. We analyzed climatologies from three satellite missions, the Atmospheric Chemistry Experiment-Fourier Transform Spectrometer (ACE-FTS), the HIgh Resolution Dynamics Limb Sounder (HIRDLS), and the Michelson Interferometer for Passive Atmospheric Sounding (MIPAS). We found a CFC-11/CFC-12 lifetime ratio of 0.47±0.08 and a CFC-12 lifetime of 112(96–133) years for ACE-FTS, a ratio of 0.46±0.07 and a lifetime of 113(97–134) years for HIRDLS, and a ratio of 0.46±0.08 and a lifetime of 114(98–136) years for MIPAS. The error-weighted, combined CFC-11/CFC-12 lifetime ratio is 0.46±0.04 and the CFC-12 lifetime estimate is 113(103–124) years. These results agree with the recent Stratosphere-troposphere Processes And their Role in Climate (SPARC) reassessment, which recommends lifetimes of 52(43–67) years and 102(88–122) years, respectively. Having smaller uncertainties than the results from other recent studies, our estimates can help to better constrain CFC-11 and CFC-12 lifetime recommendations in future scientific studies and assessments. Furthermore, the satellite observations were used to validate first simulation results from a new coupled model system, which integrates a Lagrangian chemistry transport model into a climate model. For the coupled model we found a CFC-11/CFC-12 lifetime ratio of 0.48±0.07 and a CFC-12 lifetime of 110(95–129) years, based on a 10-year perpetual run. Closely reproducing the satellite observations, the new model system will likely become a useful tool to assess the impact of advective transport, mixing, and photochemistry as well as climatological variability on the stratospheric lifetimes of long-lived tracers.

scholarly journals Nonlinear response of modeled stratospheric ozone to changes in greenhouse gases and ozone depleting substances in the recent past

2015 ◽  
Vol 15 (6) ◽  
pp. 9253-9291 ◽  
Author(s):  
S. Meul ◽  
S. Oberländer-Hayn ◽  
J. Abalichin ◽  
U. Langematz
Keyword(s):  
Greenhouse Gases ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Nonlinear Effects ◽  
Polar Regions ◽  
Recent Past ◽  
Residual Circulation ◽  
Nonlinear Processes ◽  
Ozone Depleting Substances ◽  
The Impact

Abstract. In the recent past, the evolution of stratospheric ozone (O3) was affected by both increasing ozone depleting substances (ODSs) and greenhouse gases (GHGs). The impact of the single forcings on O3 is well known. Interactions between the simultaneously increased GHG and ODS concentrations, however, can occur and lead to nonlinear O3 changes. In this study, we investigate if nonlinear processes have affected O3 changes between 1960 and 2000. This is done with an idealized set of timeslice simulations with the chemistry–climate model (CCM) EMAC. Nonlinearity leads to a net reduction of ozone decrease throughout the stratosphere, with a maximum of 1.2% at 3 hPa. The total ozone column loss between 1960 and 2000 that is mainly attributed to the ODS increase is mitigated in the extra-polar regions by up to 1.1% due to nonlinear processes. A separation of the O3 changes into the contribution from chemistry and transport shows that nonlinear interactions occur in both. In the upper stratosphere a reduced efficiency of the ClOx-catalysed O3 loss chiefly causes the nonlinear O3 increase. An enhanced formation of halogen reservoir species through the reaction with methane (CH4) reduces the abundance of halogen radicals significantly. The temperature induced deceleration of the O3 loss reaction rate in the Chapman cycle is reduced, which leads to a nonlinear O3 decrease and counteracts the increase due to ClOx. Nonlinear effects on the NOx abundance cause hemispheric asymmetric nonlinear changes of the O3 loss. Nonlinear changes in O3 transport occur in particular in the Southern Hemisphere (SH) during the months September to November. Here, the residual circulation is weakened in the lower stratosphere, which goes along with a reduced O3 transport from the tropics to high latitudes. Thus, O3 decreases in the SH polar region, but increases in the SH midlatitudes.

scholarly journals Nonlinear response of modelled stratospheric ozone to changes in greenhouse gases and ozone depleting substances in the recent past

2015 ◽  
Vol 15 (12) ◽  
pp. 6897-6911 ◽  
Author(s):  
S. Meul ◽  
S. Oberländer-Hayn ◽  
J. Abalichin ◽  
U. Langematz
Keyword(s):  
Greenhouse Gases ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Polar Regions ◽  
Recent Past ◽  
Residual Circulation ◽  
Nonlinear Processes ◽  
The Past ◽  
Ozone Depleting Substances ◽  
The Impact

Abstract. In the recent past, the evolution of stratospheric ozone (O3) was affected by both increasing ozone depleting substances (ODSs) and greenhouse gases (GHGs). The impact of the single forcings on O3 is well known. Interactions between the simultaneously increased GHG and ODS concentrations, however, can occur and lead to nonlinear O3 changes. In this study, we investigate if nonlinear processes have affected O3 changes between 1960 and 2000. This is done with an idealised set of time slice simulations with the chemistry-climate model EMAC. Due to nonlinearity the past ozone loss is diminished throughout the stratosphere, with a maximum reduction of 1.2 % at 3 hPa. The total ozone column loss between 1960 and 2000 that is mainly attributed to the ODS increase is mitigated in the extra-polar regions by up to 1.1 % due to nonlinear processes. A separation of the O3 changes into the contribution from chemistry and transport shows that nonlinear interactions occur in both. In the upper stratosphere a reduced efficiency of the ClOx-catalysed O3 loss chiefly causes the nonlinear O3 increase. An enhanced formation of halogen reservoir species through the reaction with methane (CH4) reduces the abundance of halogen radicals significantly. The temperature-induced deceleration of the O3 loss reaction rate in the Chapman cycle is reduced, which leads to a nonlinear O3 decrease and counteracts the increase due to ClOx. Nonlinear effects on the NOx abundance cause hemispheric asymmetric nonlinear changes of the O3 loss. Nonlinear changes in O3 transport occur in particular in the Southern Hemisphere (SH) during the months September to November. Here, the residual circulation is weakened in the lower stratosphere, which goes along with a reduced O3 transport from the tropics to high latitudes. Thus, O3 decreases in the SH polar region but increases in the SH midlatitudes. The existence of nonlinearities implies that future ozone change due to ODS decline slightly depends on the prevailing GHG concentrations. Therefore the future ozone evolution will not simply be a reversal of the past.

scholarly journals The representation of solar cycle signals in stratospheric ozone. Part II: Analysis of global models

2017 ◽  
Author(s):  
Amanda C. Maycock ◽  
Katja Matthes ◽  
Susann Tegtmeier ◽  
Hauke Schmidt ◽  
Rémi Thiéblemont ◽  
...  
Keyword(s):  
Solar Cycle ◽  
Solar Irradiance ◽  
Climate Models ◽  
Climate Model ◽  
Stratospheric Ozone ◽  
Temperature Response ◽  
Solar Variability ◽  
High Latitudes ◽  
Stratospheric Temperature ◽  
The Impact

Abstract. The impact of changes in incoming solar irradiance on stratospheric ozone abundances should be included in climate model simulations to fully capture the atmospheric response to solar variability. This study presents the first systematic comparison of the solar-ozone response (SOR) during the 11 year solar cycle amongst different chemistry-climate models (CCMs) and ozone databases specified in climate models that do not include chemistry. We analyse the SOR in eight CCMs from the WCRP/SPARC Chemistry-Climate Model Initiative (CCMI-1) and compare these with three ozone databases: the Bodeker Scientific database, the SPARC/AC&C database for CMIP5, and the SPARC/CCMI database for CMIP6. The results reveal substantial differences in the representation of the SOR between the CMIP5 and CMIP6 ozone databases. The peak amplitude of theSOR in the upper stratosphere (1–5 hPa) decreases from 5 % to 2 % between the CMIP5 and CMIP6 databases. This difference is because the CMIP5 database was constructed from a regression model fit to satellite observations, whereas the CMIP6 database is constructed from CCM simulations, which use a spectral solar irradiance (SSI) dataset with relatively weak UV forcing. The SOR in the CMIP6 ozone database is therefore implicitly more similar to the SOR in the CCMI-1 models than to the CMIP5 ozone database, which shows a greater resemblance in amplitude and structure to the SOR in the Bodeker database. The latitudinal structure of the annual mean SOR in the CMIP6 ozone database and CCMI-1 models is considerably smoother than in the CMIP5 database, which shows strong gradients in the SOR across the midlatitudes owing to the paucity of observations at high latitudes. The SORs in the CMIP6 ozone database and in the CCMI-1 models show a strong seasonal dependence, including large meridional gradients at mid to high latitudes during winter; such seasonal variations in the SOR are not included in the CMIP5 ozone database. Sensitivity experiments with a global atmospheric model without chemistry (ECHAM6.3) are performed to assess the impact of changes in the representation of the SOR and SSI forcing between CMIP5 and CMIP6. The experiments show that the smaller amplitude of the SOR in the CMIP6 ozone database compared to CMIP5 causes a decrease in the modelled tropical stratospheric temperature response over the solar cycle of up to 0.6 K, or around 50 % of the total amplitude. The changes in the SOR explain most of the difference in the amplitude of the tropical stratospheric temperature response in the case with combined changes in SOR and SSI between CMIP5 and CMIP6. The results emphasise the importance of adequately representing the SOR in climate models to capture the impact of solar variability on the atmosphere. Since a number of limitations in the representation of the SOR in the CMIP5 ozone database have been identified, CMIP6 models without chemistry are encouraged to use the CMIP6 ozone database to capture the climate impacts of solar variability.

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.

Influence of Ocean and Atmosphere Components on Simulated Climate Sensitivities

2013 ◽  
Vol 26 (1) ◽  
pp. 231-245 ◽  
Author(s):  
Michael Winton ◽  
Alistair Adcroft ◽  
Stephen M. Griffies ◽  
Robert W. Hallberg ◽  
Larry W. Horowitz ◽  
...  
Keyword(s):  
Sea Ice ◽  
Climate Models ◽  
Climate Model ◽  
Model Simulation ◽  
Coupled Model ◽  
Ocean Model ◽  
Historical Simulation ◽  
Model Version ◽  
Salinity Response ◽  
The Impact

Abstract The influence of alternative ocean and atmosphere subcomponents on climate model simulation of transient sensitivities is examined by comparing three GFDL climate models used for phase 5 of the Coupled Model Intercomparison Project (CMIP5). The base model ESM2M is closely related to GFDL’s CMIP3 climate model version 2.1 (CM2.1), and makes use of a depth coordinate ocean component. The second model, ESM2G, is identical to ESM2M but makes use of an isopycnal coordinate ocean model. The authors compare the impact of this “ocean swap” with an “atmosphere swap” that produces the GFDL Climate Model version 3 (CM3) by replacing the AM2 atmospheric component with AM3 while retaining a depth coordinate ocean model. The atmosphere swap is found to have much larger influence on sensitivities of global surface temperature and Northern Hemisphere sea ice cover. The atmosphere swap also introduces a multidecadal response time scale through its indirect influence on heat uptake. Despite significant differences in their interior ocean mean states, the ESM2M and ESM2G simulations of these metrics of climate change are very similar, except for an enhanced high-latitude salinity response accompanied by temporarily advancing sea ice in ESM2G. In the ESM2G historical simulation this behavior results in the establishment of a strong halocline in the subpolar North Atlantic during the early twentieth century and an associated cooling, which are counter to observations in that region. The Atlantic meridional overturning declines comparably in all three models.

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>

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