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- ItemSensitivity of polar stratospheric ozone loss to uncertainties in chemical reaction kinetics(Göttingen : Copernicus GmbH, 2009) Kawa, S.R.; Stolarski, R.S.; Newman, P.A.; Douglass, A.R.; Rex, M.; Hofmann, D.J.; Santee, M.L.; Frieler, K.The impact and significance of uncertainties in model calculations of stratospheric ozone loss resulting from known uncertainty in chemical kinetics parameters is evaluated in trajectory chemistry simulations for the Antarctic and Arctic polar vortices. The uncertainty in modeled ozone loss is derived from Monte Carlo scenario simulations varying the kinetic (reaction and photolysis rate) parameters within their estimated uncertainty bounds. Simulations of a typical winter/spring Antarctic vortex scenario and Match scenarios in the Arctic produce large uncertainty in ozone loss rates and integrated seasonal loss. The simulations clearly indicate that the dominant source of model uncertainty in polar ozone loss is uncertainty in the Cl2O 2 photolysis reaction, which arises from uncertainty in laboratory-measured molecular cross sections at atmospherically important wavelengths. This estimated uncertainty in JCl 2O2 from laboratory measurements seriously hinders our ability to model polar ozone loss within useful quantitative error limits. Atmospheric observations, however, suggest that the Cl2O2 photolysis uncertainty may be less than that derived from the lab data. Comparisons to Match, South Pole ozonesonde, and Aura Microwave Limb Sounder (MLS) data all show that the nominal recommended rate simulations agree with data within uncertainties when the Cl2O2 photolysis error is reduced by a factor of two, in line with previous in situ ClOx measurements. Comparisons to simulations using recent cross sections from Pope et al. (2007) are outside the constrained error bounds in each case. Other reactions producing significant sensitivity in polar ozone loss include BrO + ClO and its branching ratios. These uncertainties challenge our confidence in modeling polar ozone depletion and projecting future changes in response to changing halogen emissions and climate. Further laboratory, theoretical, and possibly atmospheric studies are needed.
- ItemConstructing proxy records from age models (COPRA)(München : European Geopyhsical Union, 2012) Breitenbach, S.F.M.; Rehfeld, K.; Goswami, B.; Baldin, J.U.L.; Ridley, H.E.; Kennett, D.J.; Prufer, K.M.; Aquino, V.V.; Asmerom, Y.; Polyak, V.J.; Cheng, H.; Kurths, J.; Marwan, N.Reliable age models are fundamental for any palaeoclimate reconstruction. Available interpolation procedures between age control points are often inadequately reported, and very few translate age uncertainties to proxy uncertainties. Most available modeling algorithms do not allow incorporation of layer counted intervals to improve the confidence limits of the age model in question. We present a framework that allows detection and interactive handling of age reversals and hiatuses, depth-age modeling, and proxy-record reconstruction. Monte Carlo simulation and a translation procedure are used to assign a precise time scale to climate proxies and to translate dating uncertainties to uncertainties in the proxy values. The presented framework allows integration of incremental relative dating information to improve the final age model. The free software package COPRA1.0 facilitates easy interactive usage.
- ItemEvaluation of biospheric components in earth system models using modern and palaeo-observations: The state-of-the-art(München : European Geopyhsical Union, 2013) Foley, A.M.; Dalmonech, D.; Friend, A.D.; Aires, F.; Archibald, A.T.; Bartlein, P.; Bopp, L.; Chappellaz, J.; Cox, P.; Edwards, N.R.; Feulner, G.; Friedlingstein, P.; Harrison, S.P.; Hopcroft, P.O.; Jones, C.D.; Kolassa, J.; Levine, J.G.; Prentice, I.C.; Pyle, J.; Vázquez Riveiros, N.; Wolff, E.W.; Zaehle, S.Earth system models (ESMs) are increasing in complexity by incorporating more processes than their predecessors, making them potentially important tools for studying the evolution of climate and associated biogeochemical cycles. However, their coupled behaviour has only recently been examined in any detail, and has yielded a very wide range of outcomes. For example, coupled climate–carbon cycle models that represent land-use change simulate total land carbon stores at 2100 that vary by as much as 600 Pg C, given the same emissions scenario. This large uncertainty is associated with differences in how key processes are simulated in different models, and illustrates the necessity of determining which models are most realistic using rigorous methods of model evaluation. Here we assess the state-of-the-art in evaluation of ESMs, with a particular emphasis on the simulation of the carbon cycle and associated biospheric processes. We examine some of the new advances and remaining uncertainties relating to (i) modern and palaeodata and (ii) metrics for evaluation. We note that the practice of averaging results from many models is unreliable and no substitute for proper evaluation of individual models. We discuss a range of strategies, such as the inclusion of pre-calibration, combined process- and system-level evaluation, and the use of emergent constraints, that can contribute to the development of more robust evaluation schemes. An increasingly data-rich environment offers more opportunities for model evaluation, but also presents a challenge. Improved knowledge of data uncertainties is still necessary to move the field of ESM evaluation away from a "beauty contest" towards the development of useful constraints on model outcomes.
- ItemAsymmetry and uncertainties in biogeophysical climate-vegetation feedback over a range of CO2 forcings(München : European Geopyhsical Union, 2014) Willeit, M.; Ganopolski, A.; Feulner, G.Climate–vegetation feedback has the potential to significantly contribute to climate change, but little is known about its range of uncertainties. Here, using an Earth system model of intermediate complexity we address possible uncertainties in the strength of the biogeophysical climate–vegetation feedback using a single-model multi-physics ensemble. Equilibrium experiments with halving (140 ppm) and doubling (560 ppm) of CO2 give a contribution of the vegetation–climate feedback to global temperature change in the range −0.3 to −0.1 °C and −0.1 to 0.2 °C, respectively. There is an asymmetry between warming and cooling, with a larger, positive vegetation–climate feedback in the lower CO2 climate. Hotspots of climate–vegetation feedback are the boreal zone, the Amazon rainforest and the Sahara. Albedo parameterization is the dominant source of uncertainty in the subtropics and at high northern latitudes, while uncertainties in evapotranspiration are more relevant in the tropics. We analyse the separate impact of changes in stomatal conductance, leaf area index and vegetation dynamics on climate and we find that different processes are dominant in lower and higher CO2 worlds. The reduction in stomatal conductance gives the main contribution to temperature increase for a doubling of CO2, while dynamic vegetation is the dominant process in the CO2 halving experiments. Globally the climate–vegetation feedback is rather small compared to the sum of the fast climate feedbacks. However, it is comparable to the amplitude of the fast feedbacks at high northern latitudes where it can contribute considerably to polar amplification. The uncertainties in the climate–vegetation feedback are comparable to the multi-model spread of the fast climate feedbacks.
- ItemCharacterization of organic aerosol across the global remote troposphere: A comparison of ATom measurements and global chemistry models(Katlenburg-Lindau : EGU, 2020) Hodzic, Alma; Campuzano-Jost, Pedro; Bian, Huisheng; Chin, Mian; Colarco, Peter R.; Day, Douglas A.; Froyd, Karl D.; Heinold, Bernd; Katich, Joseph M.; Jo, Duseong S.; Kodros, John K.; Nault, Benjamin A.; Pierce, Jeffrey R.; Ray, Eric; Schacht, Jacob; Schill, Gregory P.; Schroder, Jason C.; Schwarz, Joshua P.; Sueper, Donna T.; Tegen, Ina; Tilmes, Simone; Tsigaridis, Kostas; Yu, Pengfei; Jimenez, Jose L.The spatial distribution and properties of submicron organic aerosol (OA) are among the key sources of uncertainty in our understanding of aerosol effects on climate. Uncertainties are particularly large over remote regions of the free troposphere and Southern Ocean, where very few data have been available and where OA predictions from AeroCom Phase II global models span 2 to 3 orders of magnitude, greatly exceeding the model spread over source regions. The (nearly) pole-to-pole vertical distribution of nonrefractory aerosols was measured with an aerosol mass spectrometer onboard the NASA DC-8 aircraft as part of the Atmospheric Tomography (ATom) mission during the Northern Hemisphere summer (August 2016) and winter (February 2017). This study presents the first extensive characterization of OA mass concentrations and their level of oxidation in the remote atmosphere. OA and sulfate are the major contributors by mass to submicron aerosols in the remote troposphere, together with sea salt in the marine boundary layer. Sulfate was dominant in the lower stratosphere. OA concentrations have a strong seasonal and zonal variability, with the highest levels measured in the lower troposphere in the summer and over the regions influenced by biomass burning from Africa (up to 10 μgsm-3). Lower concentrations (~ 0:1 0.3 μgsm-3) are observed in the northern middle and high latitudes and very low concentrations (< 0:1 μgsm-3) in the southern middle and high latitudes. The ATom dataset is used to evaluate predictions of eight current global chemistry models that implement a variety of commonly used representations of OA sources and chemistry, as well as of the AeroCom-II ensemble. The current model ensemble captures the average vertical and spatial distribution of measured OA concentrations, and the spread of the individual models remains within a factor of 5. These results are significantly improved over the AeroCom-II model ensemble, which shows large overestimations over these regions. However, some of the improved agreement with observations occurs for the wrong reasons, as models have the tendency to greatly overestimate the primary OA fraction and underestimate the sec-ondary fraction. Measured OA in the remote free troposphere is highly oxygenated, with organic aerosol to organic carbon (OA= OC) ratios of ~ 2.2 2.8, and is 30 % 60% more oxygenated than in current models, which can lead to significant errors in OA concentrations. The model measurement comparisons presented here support the concept of a more dynamic OA system as proposed by Hodzic et al. (2016), with enhanced removal of primary OA and a stronger production of secondary OA in global models needed to provide better agreement with observations. © 2020 IEEE Computer Society. All rights reserved.
- ItemEvaluation of a three-dimensional chemical transport model (PMCAMx) in the European domain during the EUCAARI May 2008 campaign(München : European Geopyhsical Union, 2011) Fountoukis, C.; Racherla, P.N.; Denier van der Gon, H.A.C.; Polymeneas, P.; Charalampidis, P.E.; Pilinis, C.; Wiedensohler, A.; Dall'Osto, M.; O'Dowd, C.; Pandis, S.N.Sea salt aerosol can significantly affect the air quality. Sea salt can cause enhanced concentrations of particulate matter and change particle chemical composition, in particular in coastal areas, and therefore should be accounted for in air quality modelling. We have used an EMEP Unified model to calculate sea salt concentrations and depositions over Europe, focusing on studying the effects of uncertainties in sea salt production and lifetime on calculation results. Model calculations of sea salt have been compared with EMEP observations of sodium concentrations in air and precipitation for a four year period, from 2004 to 2007, including size (fine/coarse) resolved EMEP intensive measurements in 2006 and 2007. In the presented calculations, sodium air concentrations are between 8% and 46% overestimated, whereas concentrations in precipitation are systematically underestimated by 65–70% for years 2004–2007. A series of model tests have been performed to investigate the reasons for this underestimation, but further studies are needed. The model is found to reproduce the spatial distribution of Na+ in air and precipitation over Europe fairly well, and to capture most of sea salt episodes. The paper presents the main findings from a series of tests in which we compare several different sea spray source functions and also look at the effects of meteorological input and the efficiency of removal processes on calculated sea salt concentrations. Finally, sea salt calculations with the EMEP model have been compared with results from the SILAM model and observations for 2007. While the models produce quite close results for Na+ at the majority of 26 measurement sites, discrepancies in terms of bias and temporal correlation are also found. Those differences are believed to occur due to differences in the representation of source function and size distribution of sea salt aerosol, different meteorology used for model runs and the different models' resolution. This study contributes to getting a better insight on uncertainties associated with sea salt calculations and thus facilitates further improvement of aerosol modelling on both regional and global scales.
- ItemEmulating atmosphere-ocean and carbon cycle models with a simpler model, MAGICC6 - Part 2: Applications(München : European Geopyhsical Union, 2011) Meinshausen, M.; Raper, S.C.B.; Wigley, T.M.L.Intercomparisons of coupled atmosphere-ocean general circulation models (AOGCMs) and carbon cycle models are important for galvanizing our current scientific knowledge to project future climate. Interpreting such intercomparisons faces major challenges, not least because different models have been forced with different sets of forcing agents. Here, we show how an emulation approach with MAGICC6 can address such problems. In a companion paper (Meinshausen et al., 2011a), we show how the lower complexity carbon cycle-climate model MAGICC6 can be calibrated to emulate, with considerable accuracy, globally aggregated characteristics of these more complex models. Building on that, we examine here the Coupled Model Intercomparison Project's Phase 3 results (CMIP3). If forcing agents missed by individual AOGCMs in CMIP3 are considered, this reduces ensemble average temperature change from pre-industrial times to 2100 under SRES A1B by 0.4 °C. Differences in the results from the 1980 to 1999 base period (as reported in IPCC AR4) to 2100 are negligible, however, although there are some differences in the trajectories over the 21st century. In a second part of this study, we consider the new RCP scenarios that are to be investigated under the forthcoming CMIP5 intercomparison for the IPCC Fifth Assessment Report. For the highest scenario, RCP8.5, relative to pre-industrial levels, we project a median warming of around 4.6 °C by 2100 and more than 7 °C by 2300. For the lowest RCP scenario, RCP3-PD, the corresponding warming is around 1.5 °C by 2100, decreasing to around 1.1 °C by 2300 based on our AOGCM and carbon cycle model emulations. Implied cumulative CO2 emissions over the 21st century for RCP8.5 and RCP3-PD are 1881 GtC (1697 to 2034 GtC, 80% uncertainty range) and 381 GtC (334 to 488 GtC), when prescribing CO2 concentrations and accounting for uncertainty in the carbon cycle. Lastly, we assess the reasons why a previous MAGICC version (4.2) used in IPCC AR4 gave roughly 10% larger warmings over the 21st century compared to the CMIP3 average. We find that forcing differences and the use of slightly too high climate sensitivities inferred from idealized high-forcing runs were the major reasons for this difference.
- ItemConstraining ocean diffusivity from the 8.2 ka event(Berlin : Springer Verlag, 2010) Lorenz, A.; Held, H.; Bauer, E.; von Deimling, T.S.Greenland ice-core data containing the 8.2 ka event are utilized by a model-data intercomparison within the Earth system model of intermediate complexity, CLIMBER-2.3 to investigate their potential for constraining the range of uncertain ocean diffusivity properties. Within a stochastic version of the model (Bauer et al. in Paleoceanography 19:PA3014, 2004) it has been possible to mimic the pronounced cooling of the 8.2 ka event with relatively good accuracy considering the timing of the event in comparison to other modelling exercises. When statistically inferring from the 8.2 ka event on diffusivity the technical difficulty arises to establish the related likelihood numerically per realisation of the uncertain model parameters: while mainstream uncertainty analyses can assume a quasi-Gaussian shape of likelihood, with weather fluctuating around a long term mean, the 8.2 ka event as a highly nonlinear effect precludes such an a priori assumption. As a result of this study the Bayesian Analysis leads to a sharp single-mode likelihood for ocean diffusivity parameters within CLIMBER-2.3. Depending on the prior distribution this likelihood leads to a reduction of uncertainty in ocean diffusivity parameters (e. g. for flat prior uncertainty in the vertical ocean diffusivity parameter is reduced by factor 2). These results highlight the potential of paleo data to constrain uncertain system properties and strongly suggest to make further steps with more complex models and richer data sets to harvest this potential. © The Author(s) 2009.
- ItemModelling of sea salt concentrations over Europe: Key uncertainties and comparison with observations(München : European Geopyhsical Union, 2011) Tsyro, S.; Aas, W.; Soares, J.; Sofiev, M.; Berge, H.; Spindler, G.Sea salt aerosol can significantly affect the air quality. Sea salt can cause enhanced concentrations of particulate matter and change particle chemical composition, in particular in coastal areas, and therefore should be accounted for in air quality modelling. We have used an EMEP Unified model to calculate sea salt concentrations and depositions over Europe, focusing on studying the effects of uncertainties in sea salt production and lifetime on calculation results. Model calculations of sea salt have been compared with EMEP observations of sodium concentrations in air and precipitation for a four year period, from 2004 to 2007, including size (fine/coarse) resolved EMEP intensive measurements in 2006 and 2007. In the presented calculations, sodium air concentrations are between 8% and 46% overestimated, whereas concentrations in precipitation are systematically underestimated by 65–70% for years 2004–2007. A series of model tests have been performed to investigate the reasons for this underestimation, but further studies are needed. The model is found to reproduce the spatial distribution of Na+ in air and precipitation over Europe fairly well, and to capture most of sea salt episodes. The paper presents the main findings from a series of tests in which we compare several different sea spray source functions and also look at the effects of meteorological input and the efficiency of removal processes on calculated sea salt concentrations. Finally, sea salt calculations with the EMEP model have been compared with results from the SILAM model and observations for 2007. While the models produce quite close results for Na+ at the majority of 26 measurement sites, discrepancies in terms of bias and temporal correlation are also found. Those differences are believed to occur due to differences in the representation of source function and size distribution of sea salt aerosol, different meteorology used for model runs and the different models' resolution. This study contributes to getting a better insight on uncertainties associated with sea salt calculations and thus facilitates further improvement of aerosol modelling on both regional and global scales.