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IPCC Fourth Assessment Report: Climate Change 2007 |
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Climate Change 2007: Working Group I: The Physical Science Basis 2.4.5.2 Estimates of the Radiative Forcing from Models General Circulation Models constitute an important and useful tool to estimate the global mean RF associated with the cloud albedo effect of anthropogenic aerosols. The model estimates of the changes in cloud reflectance are based on forward calculations, considering emissions of anthropogenic primary particles and secondary particle production from anthropogenic gases. Since the TAR, the cloud albedo effect has been estimated in a more systematic and rigorous way (allowing, for example, for the relaxation of the fixed LWC criterion), and more modelling results are now available. Most climate models use parametrizations to relate the cloud droplet number concentration to aerosol concentration; these vary in complexity from simple empirical fits to more physically based relationships. Some models are run under an increasing greenhouse gas concentration scenario and include estimates of present-day aerosol loadings (including primary and secondary aerosol production from anthropogenic sources). These global modelling studies (Table 2.7) have a limitation arising from the underlying uncertainties in aerosol emissions (e.g., emission rates of primary particles and of secondary particle precursors). Another limitation is the inability to perform a meaningful comparison between the various model results owing to differing formulations of relationships between aerosol particle concentrations and cloud droplet or ice crystal populations; this, in turn, yields differences in the impact of microphysical changes on the optical properties of clouds. Further, even when the relationships used in different models are similar, there are noticeable differences in the spatial distributions of the simulated low-level clouds. Individual models’ physics have undergone considerable evolution, and it is difficult to clearly identify all the changes in the models as they have evolved. While GCMs have other well-known limitations, such as coarse spatial resolution, inaccurate representation of convection and hence updraft velocities leading to aerosol activation and cloud formation processes, and microphysical parametrizations, they nevertheless remain an essential tool for quantifying the global cloud albedo effect. In Table 2.7, differences in the treatment of the aerosol mixtures (internal or external, with the latter being the more frequently employed method) are noted. Case studies of droplet activation indicate a clear sensitivity to the aerosol composition (McFiggans et al., 2006); additionally, radiative transfer is sensitive to the aerosol composition and the insoluble fraction present in the cloud droplets. Table 2.7. Published model studies of the RF due to cloud albedo effect, in the context of liquid water clouds, with a listing of the relevant modelling details. Model | Model typea | Aerosol speciesb | Aerosol mixturesc | Cloud types included | Microphysics | Radiative Forcing(W m–2)d |
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Lohmann et al. (2000) | AGCM + sulphur cycle (ECHAM4) | S, OC, BC, SS, D | I | warm and mixed phase | Droplet number concentration and LWC, Beheng (1994); Sundqvist et al. (1989). Also, mass and number from field observations | –1.1 (total) –0.45 (albedo) | E | –1.5 (total) | Jones et al. (2001) | AGCM + sulphur cycle, fixed SST (Hadley) | S, SS, D (a crude attempt for D over land, no radiation) | E | stratiform and shallow cumulus | Droplet number concentration and LWC, Wilson and Ballard (1999); Smith (1990); Tripoli and Cotton (1980); Bower et al. (1994). Warm and mixed phase, radiativetreatment of anvil cirrus, non-spherical ice particles | –1.89 (total) –1.34 (albedo) | Williams et al. (2001b) | GCM with slab ocean + sulphur cycle (Hadley) | S, SS | E | stratiform and shallow cumulus | Jones et al. (2001) | –1.69 (total) –1.37 (albedo) | AGCM, fixed SST | –1.62 (total) –1.43(albedo) | Rotstayn and Penner (2001) | AGCM (CSIRO), fixed SST and sulphur loading | S | n.a. | warm and mixed phase | Rotstayn (1997); Rotstayn et al. (2000) | –1.39 (albedo) | Rotstayn and Liu (2003) value decreased) | Interactive sulphur cycle | Inclusion of dispersion | 12 to 35% decrease –1.12 (albedo, mid value decreased) | Ghan et al. (2001) | AGCM (PNNL) + chemistry (MIRAGE), fixed SST | S, OC, BC, SS, N, D | E (for different modes); I (within modes) | warm and mixed phase | Droplet number concentration and LWC, crystal concentration and ice water content. Different processes affecting the various modes | –1.7 (total) –0.85 (albedo) | Chuang et al. (2002) | CCM1 (NCAR) + chemistry (GRANTOUR), fixed SST | S, OC, BC, SS, D | E (for emitted particles); I: when growingby condensation | warm and mixed phase | Modified from Chuang and Penner (1995), no collision/coalescence | –1.85 (albedo) | Menon et al. (2002a) | GCM (GISS) + sulphur cycle, fixed SST | S,OC, SS | E | warm | Droplet number concentration and LWC, Del Genio et al. (1996), Sundqvist et al. (1989). Warm and mixed phase, improved vertical distribution of clouds (but only ninelayers).Global aerosol burdens poorly constrained | –2.41 (total) –1.55 (albedo) | Kristjansson (2002) | CCM3 (NCAR) fixed SST | S, OC, BC, SS, D | E (for nucleation mode and fossil fuel BC); I (foraccumulationmode) | warm and mixed phase | Rasch and Kristjánsson (1998). Stratiform and detraining convective clouds | –1.82 (total) –1.35 (albedo) | Suzuki et al. (2004) | AGCM (Japan), fixed SST | S, OC, BC, SS | E | stratiform | Berry(1967), Sundqvist(1978) | Errata
-0.54 (albedo) | Quaas et al. (2004) | AGCM (LMDZ) + interactive sulphur cycle, fixed SST | S | n.a. | warm and mixed phase | Aerosol mass and cloud droplet number concentration, Boucher and Lohmann (1995); Boucher et al. (1995) | –1.3 (albedo) | Hansen et al. (2005) shallow (below | GCM (GISS) + 3 different ocean parametrizations | S, OC, BC, SS, N, D (D not included in clouds) | E | warm and 720hPa) | Schmidt et al. (2005), 20 vertical layers. Droplet number concentration (Menon and Del Genio, 2007) | –0.77 (albedo) | Kristjansson et al. (2005) | CCM3 (NCAR) + sulphur and carbon cycles slab ocean | S, OC, BC, SS, D | E (for nucleation mode and fossil fuel BC); I (foraccumulationmode) | warm and mixed phase | Kristjansson (2002). Stratiform and detraining convective clouds | –1.15 (total,at the surface) | Quaas and Boucher (2005) | AGCM (LMDZ) + interactive sulphur cycle, fixed SST | S, OC, BC, SS, D | E | warm and mixed phase | Aerosol mass and cloud droplet number concentration, Boucher and Lohmann (1995); Boucher et al. (1995)control run | –0.9 (albedo) | fit to POLDER data fit to MODIS data | –0.5 (albedo)e –0.3 (albedo)e | Quaas et al. (2005) | AGCM (LMDZ and ECHAM4) | S, OC, BC, SS, D | E | warm and mixed phase | Aerosol mass and cloud droplet number concentration, Boucher and Lohmann, (1995), control runs (ctl) | –0.84 (total LMDZ-ctl) –1.54 (total(ECHAM4-ctl) | Aerosol mass and cloud droplet number concentration fitted to MODIS data | –0.53 (total LMDZ)e –0.29 (total(ECHAM4)e | Dufresne et al. (2005) | AGCM (LMDZ) + interactive sulphur cycle, fixed SST | S | n.a. | warm | Aerosol mass and cloud droplet number concentration, Boucher and Lohmann, (1995), fitted to POLDER data | –0.22 (albedo)e | Takemura et al. (2005) | AGCM (SPRINTARS) + slab ocean | S, OC, BC, SS, D | E (50% BC from fossil fuel); I (for OC and BC) | warm | Activation based on Kohler theory and updraft velocity | –0.94 (total) –0.52 (albedo) | Chen and Penner (2005) | AGCM (UM) + fixed SST | S, SS, D, OC, BC | I | warm and mixed phase | Aerosol mass and cloud droplet number concentration(lognormal)Control (Abdul-Razzak and Ghan, 2002) | –1.30 (albedo,UM_ctrl)f | Relationship between droplet concentration and dispersion coefficient: High | –0.75 (albedo,UM_1)f | Relationship between droplet concentration and dispersion coefficient: Medium Updraft velocity | –0.86 (albedo,UM_2)f –1.07 (albedo,UM_3)f | Relationship between droplet concentration and dispersion coefficient: Low Chuang et al. (1997) | –1.10 (albedo, UM_4)f –1.29 (albedo,UM_5)f | Nenes and Seinfeld (2003) | –1.79 (albedo,UM_6)f | Ming et al. (2005b) | AGCM (GFDL), fixed SST and sulphur loading | S | n.a. | warm | Rotstayn et al. (2000), Khainroutdinov and Kogan (2000). Aerosols off-line | –2.3 (total) –1.4 (albedo) | Penner et al. (2006) results from experiment 1 | LMDZ, Oslo and CCSR | S, SS, D, OC, BC | E | warm and mixed phase | Aerosol mass and cloud droplet number concentration; Boucher and Lohmann, (1995); Chen and Penner (2005); Sundqvist (1978) | –0.65 (albedo Oslo) –0.68 (albedo LMDZ) –0.74 (albedo CCSR) |
All models estimate a negative global mean RF associated with the cloud albedo effect, with the range of model results varying widely, from –0.22 to –1.85 W m–2. There are considerable differences in the treatment of aerosol, cloud processes and aerosol-cloud interaction processes in these models. Several models include an interactive sulphur cycle and anthropogenic aerosol particles composed of sulphate, as well as naturally produced sea salt, dust and continuously outgassing volcanic sulphate aerosols. Lohmann et al. (2000) and Chuang et al. (2002) included internally mixed sulphate, black and organic carbon, sea salt and dust aerosols, resulting in the most negative estimate of the cloud albedo indirect effect. Takemura et al. (2005) used a global aerosol transport-radiation model coupled to a GCM to estimate the direct and indirect effects of aerosols and their associated RF. The model includes a microphysical parametrization to diagnose the cloud droplet number concentration using Köhler theory, which depends on the aerosol particle number concentration, updraft velocity, size distributions and chemical properties of each aerosol species. The results indicate a global decrease in cloud droplet effective radius caused by anthropogenic aerosols, with the global mean RF calculated to be –0.52 W m–2; the land and oceanic contributions are –1.14 and –0.28 W m–2, respectively. Other modelling results also indicate that the mean RF due to the cloud albedo effect is on average somewhat larger over land than over oceans; over oceans there is a more consistent response from the different models, resulting in a smaller inter-model variability (Lohmann and Feichter, 2005). Chen and Penner (2005), by systematically varying parameters, obtained a less negative RF when the in-cloud updraft velocity was made to depend on the turbulent kinetic energy. Incorporating other cloud nucleation schemes, for example, changing from Abdul-Razzak and Ghan (2002) to the Chuang et al. (1997) parametrization resulted in no RF change, while changing to the Nenes and Seinfeld (2003) parametrization made the RF more negative. Rotstayn and Liu (2003) found a 12 to 35% decrease in the RF when the size dispersion effect was included in the case of sulphate particles. Chen and Penner (2005) further explored the range of parameters used in Rotstayn and Liu (2003) and found the RF to be generally less negative than in the standard integration. A model intercomparison study (Penner et al., 2006) examined the differences in cloud albedo effect between models through a series of controlled experiments that allowed examination of the uncertainties. This study presented results from three models, which were run with prescribed aerosol mass-number concentration (from Boucher and Lohmann, 1995), aerosol field (from Chen and Penner, 2005) and precipitation efficiency (from Sundqvist, 1978). The cloud albedo RFs in the three models do not vary widely: –0.65, –0.68 and –0.74 W m–2, respectively. Nevertheless, changes in the autoconversion scheme led to a differing response of the LWP between the models, and this is identified as an uncertainty. A closer inspection of the treatment of aerosol species in the models leads to a broad separation of the results into two groups: models with only a few aerosol species and those that include a more complex mixture of aerosols of different composition. Thus, in Figure 2.14, RF results are grouped according to the type of aerosol species included in the simulations. In the top panel of Figure 2.14, which shows estimates from models that mainly include anthropogenic sulphate, there is an indication that the results are converging, even though the range of models comes from studies published between 2001 and 2006. These studies show much less scatter than in the TAR, with a mean and standard deviation of –1.37 ± 0.14 W m–2. In contrast, in the bottom panel of Figure 2.14, which shows the studies that include more species, a much larger variability is found. These latter models (see Table 2.7) include ‘state of the art’ parametrizations of droplet activation for a variety of aerosols, and include both internal and external mixtures. Some studies have commented on inconsistencies between some of the earlier estimates of the cloud albedo RF from forward and inverse calculations (Anderson et al., 2003). Notwithstanding the fact that these two streams of calculations rely on very different formulations, the results here appear to be within range of the estimates from inverse calculations. |
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