[1] Simulations of the stratosphere from thirteen coupled chemistry-climate models (CCMs) are evaluated to provide guidance for the interpretation of ozone predictions made by the same CCMs. The focus of the evaluation is on how well the fields and processes that are important for determining the ozone distribution are represented in the simulations of the recent past. The core period of the evaluation is from 1980 to 1999 but long-term trends are compared for an extended period . Comparisons of polar high-latitude temperatures show that most CCMs have only small biases in the Northern Hemisphere in winter and spring, but still have cold biases in the Southern Hemisphere spring below 10 hPa. Most CCMs display the correct stratospheric response of polar temperatures to wave forcing in the Northern, but not in the Southern Hemisphere. Global long-term stratospheric temperature trends are in reasonable agreement with satellite and radiosonde observations. Comparisons of simulations of methane, mean age of air, and propagation of the annual cycle in water vapor show a wide spread in the results, indicating differences in transport. However, for around half the models there is reasonable agreement with observations. In these models the mean age of air and the water vapor tape recorder signal are generally better than reported in previous model intercomparisons. Comparisons of the water vapor and inorganic chlorine (Cl y ) fields also show a large intermodel spread. Differences in tropical water vapor mixing ratios in the lower stratosphere are primarily related to biases in the simulated tropical tropopause temperatures and not transport. The spread in Cl y , which is largest in the polar lower stratosphere, appears to be primarily related to transport differences. In general the amplitude and phase of the annual cycle in total ozone is well simulated apart from the southern high latitudes. Most CCMs show reasonable agreement with observed total D223081 of 29 ozone trends and variability on a global scale, but a greater spread in the ozone trends in polar regions in spring, especially in the Arctic. In conclusion, despite the wide range of skills in representing different processes assessed here, there is sufficient agreement between the majority of the CCMs and the observations that some confidence can be placed in their predictions. Citation: Eyring, V., et al. (2006), Assessment of temperature, trace species, and ozone in chemistry-climate model simulations of the recent past,

Abstract. We present an overview of state-of-the-art chemistry-climate and chemistry transport models that are used within phase 1 of the Chemistry-Climate Model Initiative (CCMI-1). The CCMI aims to conduct a detailed evaluation of participating models using process-oriented diagnostics derived from observations in order to gain confidence in the models' projections of the stratospheric ozone layer, tropospheric composition, air quality, where applicable global climate change, and the interactions between them. Interpretation of these diagnostics requires detailed knowledge of the radiative, chemical, dynamical, and physical processes incorporated in the models. Also an understanding of the degree to which CCMI-1 recommendations for simulations have been followed is necessary to understand model responses to anthropogenic and natural forcing and also to explain intermodel differences. This becomes even more important given the ongoing development and the ever-growing complexity of these models. This paper also provides an overview of the available CCMI-1 simulations with the aim of informing CCMI data users.

Simulations from eleven coupled chemistry‐climate models (CCMs) employing nearly identical forcings have been used to project the evolution of stratospheric ozone throughout the 21st century. The model‐to‐model agreement in projected temperature trends is good, and all CCMs predict continued, global mean cooling of the stratosphere over the next 5 decades, increasing from around 0.25 K/decade at 50 hPa to around 1 K/decade at 1 hPa under the Intergovernmental Panel on Climate Change (IPCC) Special Report on Emissions Scenarios (SRES) A1B scenario. In general, the simulated ozone evolution is mainly determined by decreases in halogen concentrations and continued cooling of the global stratosphere due to increases in greenhouse gases (GHGs). Column ozone is projected to increase as stratospheric halogen concentrations return to 1980s levels. Because of ozone increases in the middle and upper stratosphere due to GHG‐induced cooling, total ozone averaged over midlatitudes, outside the polar regions, and globally, is projected to increase to 1980 values between 2035 and 2050 and before lower‐stratospheric halogen amounts decrease to 1980 values. In the polar regions the CCMs simulate small temperature trends in the first and second half of the 21st century in midwinter. Differences in stratospheric inorganic chlorine (Cly) among the CCMs are key to diagnosing the intermodel differences in simulated ozone recovery, in particular in the Antarctic. It is found that there are substantial quantitative differences in the simulated Cly, with the October mean Antarctic Cly peak value varying from less than 2 ppb to over 3.5 ppb in the CCMs, and the date at which the Cly returns to 1980 values varying from before 2030 to after 2050. There is a similar variation in the timing of recovery of Antarctic springtime column ozone back to 1980 values. As most models underestimate peak Cly near 2000, ozone recovery in the Antarctic could occur even later, between 2060 and 2070. In the Arctic the column ozone increase in spring does not follow halogen decreases as closely as in the Antarctic, reaching 1980 values before Arctic halogen amounts decrease to 1980 values and before the Antarctic. None of the CCMs predict future large decreases in the Arctic column ozone. By 2100, total column ozone is projected to be substantially above 1980 values in all regions except in the tropics.

[1] The 11-year solar cycles in ozone and temperature are examined using new simulations of coupled chemistry climate models. The results show a secondary maximum in stratospheric tropical ozone, in agreement with satellite observations and in contrast with most previously published simulations. The mean model response varies by up to about 2.5% in ozone and 0.8 K in temperature during a typical solar cycle, at the lower end of the observed ranges of peak responses. Neither the upper atmospheric effects of energetic particles nor the presence of the quasi biennial oscillation is necessary to simulate the lower stratospheric response in the observed low latitude ozone concentration. Comparisons are also made between model simulations and observed total column ozone. As in previous studies, the model simulations agree well with observations. For those models which cover the full temporal range 1960-2005, the ozone solar signal below 50 hPa changes substantially from the first two solar cycles to the last two solar cycles. Further investigation suggests that this difference is due to an aliasing between the sea surface temperatures and the solar cycle during the first part of the period. The relationship between these results and the overall structure in the tropical solar ozone response is discussed. Further understanding of solar processes requires improvement in the observations of the vertically varying and column integrated ozone.

A new global climate model, MRI-CGCM3, has been developed at the Meteorological Research Institute (MRI). This model is an overall upgrade of MRI's former climate model MRI-CGCM2 series. MRI-CGCM3 is composed of atmosphere-land, aerosol, and ocean-ice models, and is a subset of the MRI's earth system model MRI-ESM1. Atmospheric component MRI-AGCM3 is interactively coupled with aerosol model to represent direct and indirect e¤ects of aerosols with a new cloud microphysics scheme. Basic experiments for pre-industrial control, historical and climate sensitivity are performed with MRI-CGCM3. In the pre-industrial control experiment, the model exhibits very stable behavior without climatic drifts, at least in the radiation budget, the temperature near the surface and the major indices of ocean circulations. The sea surface temperature (SST) drift is sufficiently small, while there is a 1 W m À2 heating imbalance at the surface. The model's climate sensitivity is estimated to be 2.11 K with Gregory's method. The transient climate response (TCR) to 1 % yr À1 increase of carbon dioxide (CO 2 ) concentration is 1.6 K with doubling of CO 2 concentration and 4.1 K with quadrupling of CO 2 concentration. The simulated present-day mean climate in the historical experiment is evaluated by comparison with observations, including reanalysis. The model reproduces the overall mean climate, including seasonal variation in various aspects in the atmosphere and the oceans. Variability in the simulated climate is also evaluated and is found to be realistic, including El Niñ o and Southern Oscillation and the Arctic and Antarctic oscillations. However, some important issues are identified. The simulated SST indicates generally cold bias in the Northern Hemisphere (NH) and warm bias in the Southern Hemisphere (SH), and the simulated sea ice expands excessively in the North Atlantic in winter. A double ITCZ also appears in the tropical Pacific, particularly in the austral summer.

The new Meteorological Research Institute Earth System Model version 2.0 (MRI-ESM2.0) has been developed based on previous models, MRI-CGCM3 and MRI-ESM1, which participated in the fifth phase of the Coupled Model Intercomparison Project (CMIP5). These models underwent numerous improvements meant for highly accurate climate reproducibility. This paper describes model formulation updates and evaluates basic performance of its physical components. The new model has nominal horizontal resolutions of 100 km for atmosphere and ocean components, similar to the previous models. The atmospheric vertical resolution is 80 layers, which is enhanced from the 48 layers of its predecessor. Accumulation of various improvements concerning clouds, such as a new stratocumulus cloud scheme, led to remarkable reduction in errors in shortwave, longwave, and net radiation at the top of the atmosphere. The resulting errors are sufficiently small compared with those in the CMIP5 models. The improved radiation distribution brings the accurate meridional heat transport required for the ocean and contributes to a reduced surface air temperature (SAT) bias. MRI-ESM2.0 displays realistic reproduction of both mean climate and interannual variability. For instance, the stratospheric quasi-biennial oscillation can now be realistically expressed through the enhanced vertical resolution and introduction of non-orographic gravity wave drag parameterization. For the historical experiment, MRI-ESM2.0 reasonably reproduces global SAT change

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.

Conceptual representation of interactive effects of changes in greenhouse gases and ozone-depleting substances on climate and stratospheric ozone, which together with changes in aerosols, clouds and surface reflectivity determine UV-B radiation at Earth's surface.