scholarly journals The sensitivity of stratospheric ozone changes through the 21st century to N<sub>2</sub>O and CH<sub>4</sub>

2012 ◽  
Vol 12 (23) ◽  
pp. 11309-11317 ◽  
Author(s):  
L. E. Revell ◽  
G. E. Bodeker ◽  
P. E. Huck ◽  
B. E. Williamson ◽  
E. Rozanov

Abstract. Through the 21st century, anthropogenic emissions of the greenhouse gases N2O and CH4 are projected to increase, thus increasing their atmospheric concentrations. Consequently, reactive nitrogen species produced from N2O and reactive hydrogen species produced from CH4 are expected to play an increasingly important role in determining stratospheric ozone concentrations. Eight chemistry-climate model simulations were performed to assess the sensitivity of stratospheric ozone to different emissions scenarios for N2O and CH4. Global-mean total column ozone increases through the 21st century in all eight simulations as a result of CO2-induced stratospheric cooling and decreasing stratospheric halogen concentrations. Larger N2O concentrations were associated with smaller ozone increases, due to reactive nitrogen-mediated ozone destruction. In the simulation with the largest N2O increase, global-mean total column ozone increased by 4.3 DU through the 21st century, compared with 10.0 DU in the simulation with the smallest N2O increase. In contrast, larger CH4 concentrations were associated with larger ozone increases; global-mean total column ozone increased by 16.7 DU through the 21st century in the simulation with the largest CH4 concentrations and by 4.4 DU in the simulation with the lowest CH4 concentrations. CH4 leads to ozone loss in the upper and lower stratosphere by increasing the rate of reactive hydrogen-mediated ozone loss cycles, however in the lower stratosphere and troposphere, CH4 leads to ozone increases due to photochemical smog-type chemistry. In addition to this mechanism, total column ozone increases due to H2O-induced cooling of the stratosphere, and slowing of the chlorine-catalyzed ozone loss cycles due to an increased rate of the CH4 + Cl reaction. Stratospheric column ozone through the 21st century exhibits a near-linear response to changes in N2O and CH4 surface concentrations, which provides a simple parameterization for the ozone response to changes in these gases.

2012 ◽  
Vol 12 (7) ◽  
pp. 17583-17605 ◽  
Author(s):  
L. E. Revell ◽  
G. E. Bodeker ◽  
P. E. Huck ◽  
B. E. Williamson ◽  
E. Rozanov

Abstract. Through the 21st century, anthropogenic emissions of the greenhouse gases N2O and CH4 are projected to increase, thus increasing their atmospheric concentrations. Consequently, reactive nitrogen species produced from N2O and reactive hydrogen species produced from CH4 are expected to play an increasingly important role in determining stratospheric ozone concentrations. Eight chemistry-climate model simulations were performed to assess the sensitivity of stratospheric ozone to different emissions scenarios for N2O and CH4. Increases in reactive nitrogen-mediated ozone loss resulting from increasing N2O concentrations lead to a decrease in global-mean total column ozone. Increasing CH4 concentrations increase the rate of reactive hydrogen-mediated ozone loss in the upper stratosphere. Overall however, increasing CH4 concentrations lead to an increase in global-mean total column ozone. Stratospheric column ozone over the 21st century exhibits a near-linear response to changes in N2O and CH4 surface concentrations, which provides a simple parameterization for the ozone response to changes in these gases.


2010 ◽  
Vol 10 (19) ◽  
pp. 9451-9472 ◽  
Author(s):  
V. Eyring ◽  
I. Cionni ◽  
G. E. Bodeker ◽  
A. J. Charlton-Perez ◽  
D. E. Kinnison ◽  
...  

Abstract. Projections of stratospheric ozone from a suite of chemistry-climate models (CCMs) have been analyzed. In addition to a reference simulation where anthropogenic halogenated ozone depleting substances (ODSs) and greenhouse gases (GHGs) vary with time, sensitivity simulations with either ODS or GHG concentrations fixed at 1960 levels were performed to disaggregate the drivers of projected ozone changes. These simulations were also used to assess the two distinct milestones of ozone returning to historical values (ozone return dates) and ozone no longer being influenced by ODSs (full ozone recovery). The date of ozone returning to historical values does not indicate complete recovery from ODSs in most cases, because GHG-induced changes accelerate or decelerate ozone changes in many regions. In the upper stratosphere where CO2-induced stratospheric cooling increases ozone, full ozone recovery is projected to not likely have occurred by 2100 even though ozone returns to its 1980 or even 1960 levels well before (~2025 and 2040, respectively). In contrast, in the tropical lower stratosphere ozone decreases continuously from 1960 to 2100 due to projected increases in tropical upwelling, while by around 2040 it is already very likely that full recovery from the effects of ODSs has occurred, although ODS concentrations are still elevated by this date. In the midlatitude lower stratosphere the evolution differs from that in the tropics, and rather than a steady decrease in ozone, first a decrease in ozone is simulated from 1960 to 2000, which is then followed by a steady increase through the 21st century. Ozone in the midlatitude lower stratosphere returns to 1980 levels by ~2045 in the Northern Hemisphere (NH) and by ~2055 in the Southern Hemisphere (SH), and full ozone recovery is likely reached by 2100 in both hemispheres. Overall, in all regions except the tropical lower stratosphere, full ozone recovery from ODSs occurs significantly later than the return of total column ozone to its 1980 level. The latest return of total column ozone is projected to occur over Antarctica (~2045–2060) whereas it is not likely that full ozone recovery is reached by the end of the 21st century in this region. Arctic total column ozone is projected to return to 1980 levels well before polar stratospheric halogen loading does so (~2025–2030 for total column ozone, cf. 2050–2070 for Cly+60×Bry) and it is likely that full recovery of total column ozone from the effects of ODSs has occurred by ~2035. In contrast to the Antarctic, by 2100 Arctic total column ozone is projected to be above 1960 levels, but not in the fixed GHG simulation, indicating that climate change plays a significant role.


2010 ◽  
Vol 10 (5) ◽  
pp. 11659-11710 ◽  
Author(s):  
V. Eyring ◽  
I. Cionni ◽  
G. E. Bodeker ◽  
A. J. Charlton-Perez ◽  
D. E. Kinnison ◽  
...  

Abstract. Projections of stratospheric ozone from a suite of chemistry-climate models (CCMs) have been analyzed. In addition to a reference simulation where anthropogenic halogenated ozone depleting substances (ODSs) and greenhouse gases (GHGs) vary with time, sensitivity simulations with either ODSs or GHGs concentrations fixed at 1960 levels were performed to disaggregate the drivers of projected ozone changes. These simulations were also used to assess the two distinct milestones of ozone returning to historical values (ozone return dates) and ozone no longer being influenced by ODSs (full ozone recovery). These two milestones are different. The date of ozone returning to historical values does not indicate complete recovery from ODSs in most cases, because GHG induced changes accelerate or decelerate ozone changes in many regions. In the upper stratosphere where GHG induced stratospheric cooling increases ozone, full ozone recovery has not likely occurred by 2100 while ozone returns to its 1980 or even 1960 levels well before (~2025 and 2040, respectively). In contrast, in the tropical lower stratosphere ozone decreases continuously from 1960 to 2100 due to projected increases in tropical upwelling, while by around 2040 it is already very likely that full recovery from the effects of ODSs has occurred, although ODS concentrations are still elevated by this date. In the lower midlatitude stratosphere the evolution differs from that in the tropics, and rather than a steady decrease of ozone, first a decrease of ozone is simulated between 1960 and 2000, which is then followed by a steady increase throughout the 21st century. Ozone in the lower stratosphere midlatitudes returns to its 1980 levels ${\\sim}$2045 in the NH and ~2055 in the SH, and full ozone recovery is likely reached by 2100 in both hemispheres. Overall, in all regions except the tropical lower stratosphere, full ozone recovery from ODSs occurs significantly later than the return of total column ozone to its 1980 level. The latest return of total column ozone is projected to occur over Antarctica (~2050–2060) whereas it is not likely that full ozone recovery is reached by the end of the 21st century in this region. Arctic total column ozone is projected to return to 1980 levels well before Cly does so (~2020–2030) and while it is likely that full recovery of ozone from the effects of ODSs has occurred by ~2035, at no time before 2100 is it very likely that full recovery has occurred. In contrast to the Antarctic, by 2100 Arctic total column ozone is projected to be above 1960 levels, but not in the fixed GHG simulation, indicating that climate change plays a significant role.


2018 ◽  
Vol 18 (2) ◽  
pp. 1379-1394 ◽  
Author(s):  
William T. Ball ◽  
Justin Alsing ◽  
Daniel J. Mortlock ◽  
Johannes Staehelin ◽  
Joanna D. Haigh ◽  
...  

Abstract. Ozone forms in the Earth's atmosphere from the photodissociation of molecular oxygen, primarily in the tropical stratosphere. It is then transported to the extratropics by the Brewer–Dobson circulation (BDC), forming a protective ozone layer around the globe. Human emissions of halogen-containing ozone-depleting substances (hODSs) led to a decline in stratospheric ozone until they were banned by the Montreal Protocol, and since 1998 ozone in the upper stratosphere is rising again, likely the recovery from halogen-induced losses. Total column measurements of ozone between the Earth's surface and the top of the atmosphere indicate that the ozone layer has stopped declining across the globe, but no clear increase has been observed at latitudes between 60° S and 60° N outside the polar regions (60–90°). Here we report evidence from multiple satellite measurements that ozone in the lower stratosphere between 60° S and 60° N has indeed continued to decline since 1998. We find that, even though upper stratospheric ozone is recovering, the continuing downward trend in the lower stratosphere prevails, resulting in a downward trend in stratospheric column ozone between 60° S and 60° N. We find that total column ozone between 60° S and 60° N appears not to have decreased only because of increases in tropospheric column ozone that compensate for the stratospheric decreases. The reasons for the continued reduction of lower stratospheric ozone are not clear; models do not reproduce these trends, and thus the causes now urgently need to be established.


2017 ◽  
Author(s):  
James Keeble ◽  
Ewa M. Bednarz ◽  
Antara Banerjee ◽  
N. Luke Abraham ◽  
Neil R. P. Harris ◽  
...  

Abstract. Chemical and dynamical drivers of trends in tropical total column ozone (TCO3) for the recent past and future periods are explored using the UM-UKCA chemistry-climate model. A transient 1960-2100 simulation is analysed which follows the representative concentration pathway 6.0 (RCP6.0) emissions scenario for the future. Tropical averaged (10° S–10° N) TCO3 values decrease from the 1970s, reaching a minimum around 2000, and return to their 1980 values around 2040, consistent with the use and emission of ozone depleting substances (ODS), and their later controls under the Montreal Protocol. However, when the ozone column is subdivided into three partial columns (PCO3) that cover the upper stratosphere (PCO3US), lower stratosphere (PCO3LS) and troposphere (PCO3T), significant differences to the behaviour of the total column are seen. Modelled PCO3T values increase from 1960–2000 before remaining steady under this particular emissions scenario throughout the 21st century. PCO3LS values decrease rapidly from 1960–2000, remain steady until around 2050, before gradually decreasing further to 2100, never recovering to their 1980s values. PCO3US values decrease from 1960–2000, before rapidly increasing throughout the 21st century, recovering to 1980s values by ~ 2020, and are significantly higher than 1980s values by 2100. Using a series of idealised UM-UKCA time-slice simulations with varying concentrations of well-mixed greenhouse gases (GHG) and ODS set to either year 2000 or 2100 levels, we examine the main processes that drive the PCO3 responses in the three regions, and assess how these processes change under different emission scenarios. Finally, we present a simple, linearised model to describe the future evolution of tropical stratospheric column ozone values based on terms representing time-dependent abundances of GHG and ODS.


2018 ◽  
Vol 18 (11) ◽  
pp. 8409-8438 ◽  
Author(s):  
Sandip S. Dhomse ◽  
Douglas Kinnison ◽  
Martyn P. Chipperfield ◽  
Ross J. Salawitch ◽  
Irene Cionni ◽  
...  

Abstract. >We analyse simulations performed for the Chemistry-Climate Model Initiative (CCMI) to estimate the return dates of the stratospheric ozone layer from depletion caused by anthropogenic stratospheric chlorine and bromine. We consider a total of 155 simulations from 20 models, including a range of sensitivity studies which examine the impact of climate change on ozone recovery. For the control simulations (unconstrained by nudging towards analysed meteorology) there is a large spread (±20 DU in the global average) in the predictions of the absolute ozone column. Therefore, the model results need to be adjusted for biases against historical data. Also, the interannual variability in the model results need to be smoothed in order to provide a reasonably narrow estimate of the range of ozone return dates. Consistent with previous studies, but here for a Representative Concentration Pathway (RCP) of 6.0, these new CCMI simulations project that global total column ozone will return to 1980 values in 2049 (with a 1σ uncertainty of 2043–2055). At Southern Hemisphere mid-latitudes column ozone is projected to return to 1980 values in 2045 (2039–2050), and at Northern Hemisphere mid-latitudes in 2032 (2020–2044). In the polar regions, the return dates are 2060 (2055–2066) in the Antarctic in October and 2034 (2025–2043) in the Arctic in March. The earlier return dates in the Northern Hemisphere reflect the larger sensitivity to dynamical changes. Our estimates of return dates are later than those presented in the 2014 Ozone Assessment by approximately 5–17 years, depending on the region, with the previous best estimates often falling outside of our uncertainty range. In the tropics only around half the models predict a return of ozone to 1980 values, around 2040, while the other half do not reach the 1980 value. All models show a negative trend in tropical total column ozone towards the end of the 21st century. The CCMI models generally agree in their simulation of the time evolution of stratospheric chlorine and bromine, which are the main drivers of ozone loss and recovery. However, there are a few outliers which show that the multi-model mean results for ozone recovery are not as tightly constrained as possible. Throughout the stratosphere the spread of ozone return dates to 1980 values between models tends to correlate with the spread of the return of inorganic chlorine to 1980 values. In the upper stratosphere, greenhouse gas-induced cooling speeds up the return by about 10–20 years. In the lower stratosphere, and for the column, there is a more direct link in the timing of the return dates of ozone and chlorine, especially for the large Antarctic depletion. Comparisons of total column ozone between the models is affected by different predictions of the evolution of tropospheric ozone within the same scenario, presumably due to differing treatment of tropospheric chemistry. Therefore, for many scenarios, clear conclusions can only be drawn for stratospheric ozone columns rather than the total column. As noted by previous studies, the timing of ozone recovery is affected by the evolution of N2O and CH4. However, quantifying the effect in the simulations analysed here is limited by the few realisations available for these experiments compared to internal model variability. The large increase in N2O given in RCP 6.0 extends the ozone return globally by ∼ 15 years relative to N2O fixed at 1960 abundances, mainly because it allows tropical column ozone to be depleted. The effect in extratropical latitudes is much smaller. The large increase in CH4 given in the RCP 8.5 scenario compared to RCP 6.0 also lengthens ozone return by ∼ 15 years, again mainly through its impact in the tropics. Overall, our estimates of ozone return dates are uncertain due to both uncertainties in future scenarios, in particular those of greenhouse gases, and uncertainties in models. The scenario uncertainty is small in the short term but increases with time, and becomes large by the end of the century. There are still some model–model differences related to well-known processes which affect ozone recovery. Efforts need to continue to ensure that models used for assessment purposes accurately represent stratospheric chemistry and the prescribed scenarios of ozone-depleting substances, and only those models are used to calculate return dates. For future assessments of single forcing or combined effects of CO2, CH4, and N2O on the stratospheric column ozone return dates, this work suggests that it is more important to have multi-member (at least three) ensembles for each scenario from every established participating model, rather than a large number of individual models.


2018 ◽  
Author(s):  
Sandip Dhomse ◽  
Douglas Kinnison ◽  
Martyn P. Chipperfield ◽  
Irene Cionni ◽  
Michaela Hegglin ◽  
...  

Abstract. We analyse simulations performed for the Chemistry-Climate Model Initiative (CCMI) to estimate the return dates of the stratospheric ozone layer from depletion caused by anthropogenic stratospheric chlorine and bromine. We consider a total of 155 simulations from 20 models, including a range of sensitivity studies which examine the impact of climate change on ozone recovery. For the control simulations (unconstrained by nudging towards analysed meteorology) there is a large spread (±20 DU in the global average) in the predictions of the absolute ozone column. Therefore, the model results need to be adjusted for biases against historical data. Also, the interannual variability in the model results need to be smoothed in order to provide a reasonably narrow estimate of the range of ozone return dates. Consistent with previous studies, but here for a Representative Concentration Pathway (RCP) of 6.0, these new CCMI simulations project that global total column ozone will return to 1980 values in 2047 (with a 1-σ uncertainty of 2042–2052). At Southern Hemisphere mid-latitudes column ozone is projected to return to 1980 values in 2046 (2042–2050), and at Northern Hemisphere mid-latitudes in 2034 (2024–2044). In the polar regions, the return dates are 2062 (2055–2066) in the Antarctic in October and 2035 (2025–2040) in the Arctic in March. The earlier return dates in the NH reflect the larger sensitivity to dynamical changes. Our estimates of return dates are later than those presented in the 2014 Ozone Assessment by approximately 5–15 years, depending on the region. In the tropics only around half the models predict a return to 1980 values, at around 2040, while the other half do not reach this value. All models show a negative trend in tropical total column ozone towards the end of the 21st century. The CCMI models generally agree in their simulation of the time evolution of stratospheric chlorine, which is the main driver of ozone loss and recovery. However, there are a few outliers which show that the multi-model mean results for ozone recovery are not as tightly constrained as possible. Throughout the stratosphere the spread of ozone return dates to 1980 values between models tends to correlate with the spread of the return of inorganic chlorine to 1980 values. In the upper stratosphere, greenhouse gas-induced cooling speeds up the return by about 10–20 years. In the lower stratosphere, and for the column, there is a more direct link in the timing of the return dates, especially for the large Antarctic depletion. Comparisons of total column ozone between the models is affected by different predictions of the evolution of tropospheric ozone within the same scenario, presumably due to differing treatment of tropospheric chemistry. Therefore, for many scenarios, clear conclusions can only be drawn for stratospheric ozone columns rather than the total column. As noted by previous studies, the timing of ozone recovery is affected by the evolution of N2O and CH4. However, the effect in the simulations analysed here is small and at the limit of detectability from the few realisations available for these experiments compared to internal model variability. The large increase in N2O given in RCP 6.0 extends the ozone return globally by ~ 15 years relative to N2O fixed at 1960 abundances, mainly because it allows tropical column ozone to be depleted. The effect in extratropical latitudes is much smaller. The large increase in CH4 given in the RCP 8.5 scenario compared to RCP 6.0 also changes ozone return by ~ 15 years, again mainly through its impact in the tropics. For future assessments of single forcing or combined effects of CO2, CH4, and N2O on the stratospheric column ozone return dates, this work suggests that is more important to have multi-member (at least 3) ensembles for each scenario from each established participating model, rather than a large number of individual models.


2008 ◽  
Vol 8 (6) ◽  
pp. 20223-20237 ◽  
Author(s):  
F. Li ◽  
R. S. Stolarski ◽  
P. A. Newman

Abstract. Vertical and latitudinal changes in the stratospheric ozone in the post-chlorofluorocarbon (CFC) era are investigated using simulations of the recent past and the 21st century with a coupled chemistry-climate model. Model results reveal that, in the 2060s when the stratospheric halogen loading is projected to return to its 1980 values, the extratropical column ozone is significantly higher than that in 1975–1984, but the tropical column ozone does not recover to 1980 values. Upper and lower stratospheric ozone changes in the post-CFC era have very different patterns. Above 15 hPa ozone increases almost latitudinally uniformly by 6 Dobson Unit (DU), whereas below 15 hPa ozone decreases in the tropics by 8 DU and increases in the extratropics by up to 16 DU. The upper stratospheric ozone increase is a photochemical response to greenhouse gas induced strong cooling, and the lower stratospheric ozone changes are consistent with enhanced mean advective transport due to a stronger Brewer-Dobson circulation. The model results suggest that the strengthening of the Brewer-Dobson circulation plays a crucial role in ozone recovery and ozone distributions in the post-CFC era.


2008 ◽  
Vol 8 (2) ◽  
pp. 251-264 ◽  
Author(s):  
R. Müller ◽  
J.-U. Grooß ◽  
C. Lemmen ◽  
D. Heinze ◽  
M. Dameris ◽  
...  

Abstract. We investigate the extent to which quantities that are based on total column ozone are applicable as measures of ozone loss in the polar vortices. Such quantities have been used frequently in ozone assessments by the World Meteorological Organization (WMO) and also to assess the performance of chemistry-climate models. The most commonly considered quantities are March and October mean column ozone poleward of geometric latitude 63° and the spring minimum of daily total ozone minima poleward of a given latitude. Particularly in the Arctic, the former measure is affected by vortex variability and vortex break-up in spring. The minimum of daily total ozone minima poleward of a particular latitude is debatable, insofar as it relies on one single measurement or model grid point. We find that, for Arctic conditions, this minimum value often occurs in air outside the polar vortex, both in the observations and in a chemistry-climate model. Neither of the two measures shows a good correlation with chemical ozone loss in the vortex deduced from observations. We recommend that the minimum of daily minima should no longer be used when comparing polar ozone loss in observations and models. As an alternative to the March and October mean column polar ozone we suggest considering the minimum of daily average total ozone poleward of 63° equivalent latitude in spring (except for winters with an early vortex break-up). Such a definition both obviates relying on one single data point and reduces the impact of year-to-year variability in the Arctic vortex break-up on ozone loss measures. Further, this measure shows a reasonable correlation (r=–0.75) with observed chemical ozone loss. Nonetheless, simple measures of polar ozone loss must be used with caution; if possible, it is preferable to use more sophisticated measures that include additional information to disentangle the impact of transport and chemistry on ozone.


2017 ◽  
Author(s):  
Olaf Morgenstern ◽  
Hideharu Akiyoshi ◽  
Yousuke Yamashita ◽  
Douglas E. Kinnison ◽  
Rolando R. Garcia ◽  
...  

Abstract. Ozone fields simulated for the Chemistry-Climate Model Initiative (CCMI) will be used as forcing data in the 6th Coupled Model Intercomparison Project (CMIP6). Here we assess, using reference and sensitivity simulations produced for phase 1 of CCMI, the suitability of CCMI-1 model results for this process, investigating the degree of consistency amongst models regarding their responses to variations in individual forcings. We consider the influences of methane, nitrous oxide, a combination of chlorinated or brominated ozone-depleting substances (ODSs), and a combination of carbon dioxide and other greenhouse gases (GHGs). We find varying degrees of consistency in the models' responses in ozone to these individual forcings, including some considerable disagreement. In particular, the response of total-column ozone to these forcings is less consistent across the multi-model ensemble than profile comparisons. The likely cause of this is lower-stratospheric transport and dynamical responses exhibiting substantial inter-model differences. The findings imply that the ozone fields derived from CCMI-1 are subject to considerable uncertainties regarding the impacts of these anthropogenic forcings.


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