Revell L.E.,NIWA - National Institute of Water and Atmospheric Research |
Revell L.E.,University of Canterbury |
Bodeker G.E.,Bodeker Scientific |
Huck P.E.,Bodeker Scientific |
And 3 more authors.
Atmospheric Chemistry and Physics | Year: 2012
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 CH 4 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 Author(s).
Garny H.,German Aerospace Center |
Grewe V.,German Aerospace Center |
Dameris M.,German Aerospace Center |
Bodeker G.E.,Bodeker Scientific |
Stenke A.,ETH Zurich
Geoscientific Model Development | Year: 2011
Chemistry-climate models (CCMs) are commonly used to simulate the past andfuture development of Earth's ozone layer. The fully coupled chemistryschemes calculate the chemical production and destruction of ozoneinteractively and ozone is transported by the simulated atmospheric flow. Dueto the complexity of the processes acting on ozone it is not straightforwardto disentangle the influence of individual processes on the temporaldevelopment of ozone concentrations. A method is introduced here thatquantifies the influence of chemistry and transport on ozone concentrationchanges and that is easily implemented in CCMs and chemistry-transport models(CTMs). In this method, ozone tendencies (i.e. the time rate of change ofozone) are partitioned into a contribution from ozone production anddestruction (chemistry) and a contribution from transport of ozone(dynamics). The influence of transport on ozone in a specific region isfurther divided into export of ozone out of that region and import of ozonefrom elsewhere into that region. For this purpose, a diagnostic is used thatdisaggregates the ozone mixing ratio field into 9 separate fields accordingto in which of 9 predefined regions of the atmosphere the ozone originated.With this diagnostic the ozone mass fluxes between these regions areobtained. Furthermore, this method is used here to attribute long-termchanges in ozone to chemistry and transport. The relative change in ozonefrom one period to another that is due to changes in production ordestruction rates, or due to changes in import or export of ozone, arequantified. As such, the diagnostics introduced here can be used to attributechanges in ozone on monthly, interannual and long-term time-scales to theresponsible mechanisms. Results from a CCM simulation are shown here asexamples, with the main focus of the paper being on introducing the method. © Author(s) 2011.
Kuttippurath J.,University Pierre and Marie Curie |
Bodeker G.E.,Bodeker Scientific |
Roscoe H.K.,British Antarctic Survey |
Nair P.J.,Center for Earth Science Studies
Geophysical Research Letters | Year: 2015
Equivalent effective stratospheric chlorine (EESC) construct of ozone regression models attributes ozone changes to EESC changes using a single value of the sensitivity of ozone to EESC over the whole period. Using space-based total column ozone (TCO) measurements, and a synthetic TCO time series constructed such that EESC does not fall below its late 1990s maximum, we demonstrate that the EESC-based estimates of ozone changes in the polar regions (70-90°) after 2000 may, falsely, suggest an EESC-driven increase in ozone over this period. An EESC-based regression of our synthetic "failed Montreal Protocol with constant EESC" time series suggests a positive TCO trend that is statistically significantly different from zero over 2001-2012 when, in fact, no recovery has taken place. Our analysis demonstrates that caution needs to be exercised when using explanatory variables, with a single fit coefficient, fitted to the entire data record, to interpret changes in only part of the record. Key Points Presents a thorough analysis on the EESC-based regression The EESC-based regression is inappropriate for estimating ozone trends Recommends a reinterpretation of the previous EESC-based trend estimates ©2014. American Geophysical Union. All Rights Reserved.
Cionni I.,German Aerospace Center |
Eyring V.,German Aerospace Center |
Lamarque J.F.,U.S. National Center for Atmospheric Research |
Randel W.J.,U.S. National Center for Atmospheric Research |
And 7 more authors.
Atmospheric Chemistry and Physics | Year: 2011
A continuous tropospheric and stratospheric vertically resolved ozone time series, from 1850 to 2099, has been generated to be used as forcing in global climate models that do not include interactive chemistry. A multiple linear regression analysis of SAGE I+II satellite observations and polar ozonesonde measurements is used for the stratospheric zonal mean dataset during the well-observed period from 1979 to 2009. In addition to terms describing the mean annual cycle, the regression includes terms representing equivalent effective stratospheric chlorine (EESC) and the 11-yr solar cycle variability. The EESC regression fit coefficients, together with pre-1979 EESC values, are used to extrapolate the stratospheric ozone time series backward to 1850. While a similar procedure could be used to extrapolate into the future, coupled chemistry climate model (CCM) simulations indicate that future stratospheric ozone abundances are likely to be significantly affected by climate change, and capturing such effects through a regression model approach is not feasible. Therefore, the stratospheric ozone dataset is extended into the future (merged in 2009) with multi-model mean projections from 13 CCMs that performed a simulation until 2099 under the SRES (Special Report on Emission Scenarios) A1B greenhouse gas scenario and the A1 adjusted halogen scenario in the second round of the Chemistry-Climate Model Validation (CCMVal-2) Activity. The stratospheric zonal mean ozone time series is merged with a three-dimensional tropospheric data set extracted from simulations of the past by two CCMs (CAM3.5 and GISS-PUCCINI) and of the future by one CCM (CAM3.5). The future tropospheric ozone time series continues the historical CAM3.5 simulation until 2099 following the four different Representative Concentration Pathways (RCPs). Generally good agreement is found between the historical segment of the ozone database and satellite observations, although it should be noted that total column ozone is overestimated in the southern polar latitudes during spring and tropospheric column ozone is slightly underestimated. Vertical profiles of tropospheric ozone are broadly consistent with ozonesondes and in-situ measurements, with some deviations in regions of biomass burning. The tropospheric ozone radiative forcing (RF) from the 1850s to the 2000s is 0.23 W m-2, lower than previous results. The lower value is mainly due to (i) a smaller increase in biomass burning emissions; (ii) a larger influence of stratospheric ozone depletion on upper tropospheric ozone at high southern latitudes; and possibly (iii) a larger influence of clouds (which act to reduce the net forcing) compared to previous radiative forcing calculations. Over the same period, decreases in stratospheric ozone, mainly at high latitudes, produce a RF of g-0.08 W m-2, which is more negative than the central Intergovernmental Panel on Climate Change (IPCC) Fourth Assessment Report (AR4) value of-0.05 W m-2, but which is within the stated range of-0.15 to +0.05 W m-2. The more negative value is explained by the fact that the regression model simulates significant ozone depletion prior to 1979, in line with the increase in EESC and as confirmed by CCMs, while the AR4 assumed no change in stratospheric RF prior to 1979. A negative RF of similar magnitude persists into the future, although its location shifts from high latitudes to the tropics. This shift is due to increases in polar stratospheric ozone, but decreases in tropical lower stratospheric ozone, related to a strengthening of the Brewer-Dobson circulation, particularly through the latter half of the 21st century. Differences in trends in tropospheric ozone among the four RCPs are mainly driven by different methane concentrations, resulting in a range of tropospheric ozone RFs between 0.4 and 0.1 W m-2 by 2100. The ozone dataset described here has been released for the Coupled Model Intercomparison Project (CMIP5) model simulations in netCDF Climate and Forecast (CF) Metadata Convention at the PCMDI website (http://cmip-pcmdi.llnl.gov/). © 2011 Author(s).
Hassler B.,University of Colorado at Boulder |
Hassler B.,National Oceanic and Atmospheric Administration |
Young P.J.,University of Colorado at Boulder |
Young P.J.,National Oceanic and Atmospheric Administration |
And 6 more authors.
Atmospheric Chemistry and Physics | Year: 2013
Climate models that do not simulate changes in stratospheric ozone concentrations require the prescription of ozone fields to accurately calculate UV fluxes and stratospheric heating rates. In this study, three different global ozone time series that are available for this purpose are compared: the data set of Randel and Wu (2007) (RW07), Cionni et al. (2011) (SPARC), and Bodeker et al. (2013) (BDBP). All three data sets represent multiple-linear regression fits to vertically resolved ozone observations, resulting in a spatially and temporally continuous stratospheric ozone field covering at least the period from 1979 to 2005. The main differences among the data sets result from regression models, which use different observations and include different basis functions. The data sets are compared against ozonesonde and satellite observations to assess how the data sets represent concentrations, trends and interannual variability. In the Southern Hemisphere polar region, RW07 and SPARC underestimate the ozone depletion in spring ozonesonde measurements. A piecewise linear trend regression is performed to estimate the 1979-1996 ozone decrease globally, covering a period of extreme depletion in most regions. BDBP overestimates Arctic and tropical ozone depletion over this period relative to the available measurements, whereas the depletion is underestimated in RW07 and SPARC. While the three data sets yield ozone concentrations that are within a range of different observations, there is a large spread in their respective ozone trends. One consequence of this is differences of almost a factor of four in the calculated stratospheric ozone radiative forcing between the data sets (RW07: -0.038 Wm-2, SPARC: -0.033 Wm-2, BDBP: -0.119 Wm-2), important in assessing the contribution of stratospheric ozone depletion to the total anthropogenic radiative forcing. © 2013 Author(s).