1. Introduction
In the Fourth Assessment Report of the Intergovernmental Panel on Climate Change (IPCC AR4), the best guess and likely range (66% probability) of global temperature warming by 2100 were 1.8 (1.1–2.9), 2.4 (1.4–3.8), 2.4 (1.4–3.8), 2.8 (1.7–4.4), 3.4 (2.0–5.4), and 4.0 (2.4–6.4) for the B1, B2, A1T, A1B, A2, and A1FI illustrative Special Report on Emissions Scenarios (SRES), respectively (Meehl et al. 2007). One can easily note that the best guess is not centered in the likely range interval; the distribution is asymmetrical with a −40/+60% distribution around the best estimate (i.e., the average of the likely range is 10% above the best estimate). This asymmetrical “−40/+60%” distribution was based on several lines of evidence as described in detail in Knutti et al. (2008). It was argued that the projected warming as simulated by 23 atmosphere–ocean general circulation models (AOGCMs) at that time, as part of the World Climate Research Programme’s phase 3 of the Coupled Model Intercomparison Project (WCRP CMIP3) (Meehl et al. 2007), did not explore the full range of possible warming for a given scenario. Although estimating such a full range is virtually impossible, one can use other lines of evidence to estimate whether the full uncertainty ranges are offset (i.e., to correct a potential bias), are wider (i.e., to reflect additional uncertainties), and/or are more or less skewed (i.e., to reflect additional skewed uncertainties).
When providing best-estimate projections and uncertainty ranges for emission scenarios, there are two major sources of uncertainty that need to be taken into account. The first relates to physical processes and feedbacks, and the uncertainty they induce on climate response for a given greenhouse gas (GHG) concentration and aerosol forcing in terms of the global-mean temperature response, and regional climate change; while the second relates to carbon cycle processes and feedbacks, with the associated uncertainty on the relationship between CO2 emissions and CO2 concentration.
A lack of understanding and observations of physical feedbacks reflected in model spread is indeed the main source of uncertainty in long-term climate projections (e.g., Hawkins and Sutton 2009). While the initial Planck response to an increase in atmospheric CO2 is known, the cascade of feedbacks arising from the warming-induced changes in water vapor, lapse rate, clouds, snow, and ice is far from being completely understood (Bony et al. 2006). The equilibrium climate sensitivity (ECS), defined as the equilibrium global mean surface warming for a doubling of atmospheric CO2, was estimated to be 3.3° ± 0.7°C (1σ,) for the slab ocean versions of CMIP3 climate models included in the IPCC AR4 (Meehl et al. 2007). A lower mean ECS was found for the coupled model versions and estimated to be 2.8°C by Forster and Taylor (2006) and 2.9°C by Meinshausen et al. (2011a). Taking into account multiple lines of evidence, the IPCC AR4 concluded: “The equilibrium climate sensitivity is likely to be in the range 2°C to 4.5°C with a best estimate of about 3°C, and is very unlikely to be less than 1.5°C. Values substantially higher than 4.5°C cannot be excluded, but agreement of models with observations is not as good for those values” (Solomon et al. 2007, p. 12). ECS being outside the CMIP3 range was possible—and in particular, no very likely statement was given for the upper end of the range.
The second major cause for uncertainties relates to the global carbon cycle. CMIP3 models were driven by CO2 concentrations along with non-CO2 GHG and aerosol forcing for each SRES scenario (Nakicenovic et al. 2000) provided by a former version of the Bern carbon cycle–climate model (Bern-CC). In the real world, changes in atmospheric CO2 concentration result from the imbalance between CO2 emissions from fossil fuel burning and deforestation (Friedlingstein et al. 2010; Peters et al. 2012) and CO2 uptake by the oceans and the terrestrial biosphere (Le Quéré et al. 2009; Denman et al. 2007). Processes controlling these uptakes as well as their response to change in atmospheric composition (mainly CO2) and climate are far from being well understood. For about two decades now, land and ocean carbon cycle models have been attempting to simulate the historical and/or future evolution of the carbon cycle with very modest improvement in terms of uncertainty reduction (e.g., VEMAP 1995; Cramer et al. 2001; Orr et al. 2001; Friedlingstein et al. 2006; Sitch et al. 2008). At the time of AR4, the Coupled Carbon Cycle Climate Model Intercomparison Project (C4MIP) highlighted the large uncertainty in future projections of the carbon cycle (Friedlingstein et al. 2006). Starting from the same historical and twenty-first-century anthropogenic emissions of CO2, 11 carbon cycle climate models (hereafter C4MIP models; model names listed in Table 1) simulated atmospheric CO2 ranging between 700 and 1000 ppm by 2100 for the SRES A2 emission scenario. Reasons for this large range were mainly due to the large uncertainty in the response of land carbon cycle to increasing CO2 (carbon–concentration feedback) and climate change (carbon–climate feedback) (Friedlingstein et al. 2006; Gregory et al. 2009). Ocean carbon cycle models showed a more consistent picture. However, two models [L’Institut Pierre-Simon Laplace Coupled Model, version 2C (IPSL-CM2C) and University of Maryland (UMD)] showed a substantial deviation from the bulk of the C4MIP models, featuring substantially higher ocean carbon uptake. Nevertheless, it was found that on average, the C4MIP models were simulating a larger atmospheric CO2 than the one prescribed to the standard CMIP3 climate models used in AR4 for climate projections, at that time based on a reference simulation with the Bern-CC. As a result, the C4MIP warming range was higher than the CMIP3 models’ warming range, and critically important, it was found that the upper end of the C4MIP models’ warming was significantly larger than the one simulated by the CMIP3 models (Meehl et al. 2007).
CMIP5 ESMs used in the study.
The combined uncertainty in climate response and carbon cycle response led to a decision, based on expert judgment, to expand the range of global temperature projections (Meehl et al. 2007; Knutti et al. 2008). The CMIP3 multimodel average was used, but the range was calculated using a −40%/+60% scaling factor as discussed above. The choice of those particular values was also based on a number of different quantitative methods using a variety of models and statistical methods, considering uncertainties in radiative forcing, climate feedbacks, ocean heat uptake, and the carbon cycle derived from models and observations (see Knutti et al. 2008, and references therein).
The World Climate Research Programme’s phase 5 of the CMIP (CMIP5) is the main resource for the IPCC AR5 assessment of climate projection. Even if the models perform well, there is no a priori reason that an ensemble of opportunity, in which the sampling of the models is not designed in any particular way, should cover all the relevant uncertainties (Tebaldi and Knutti 2007). We investigate whether a potential offset is necessary, by comparing the earth system models’ (ESMs) results of the emission-driven CMIP5 runs to the prescribed CO2 concentrations, and put that in the context of the findings at the time of the IPCC AR4. The aim of this paper is to describe the CMIP5 simulations driven by CO2 emissions and to analyze their results in terms of the carbon cycle response, thereby assessing whether the standard CMIP5 climate simulations (with prescribed atmospheric CO2) might have resulted in significantly different climate projection ranges if they were emission-driven—not concentration driven—experiments. The assessment of CMIP5 models’ transient climate response and whether it does explore the possible range, as well as an assessment of potential bias in non-CO2 forcing (e.g., aerosols), are not in the scope of this paper. Hence, this paper will not give a definitive answer on what scaling would have to be used if the CMIP5 results should be transformed to estimated climate projections for emission-driven runs. We will only attempt to quantify the additional uncertainty arising from the carbon cycle.
Section 2 below describes the CMIP5 experiments used here; section 3 presents the historical simulations and their evaluation against observations; sections 4 and 5 analyze the twenty-first-century changes in CO2, temperature, and the global carbon cycle.
2. CMIP5 experiments, emission-driven protocol, and model implementations
Despite the importance of the carbon cycle and its feedback on the climate system, the CMIP5 experiment protocol was designed to allow participation of groups having a climate model without an interactive carbon cycle as well as groups having an ESM including the global carbon cycle (Hibbard et al. 2007; Taylor et al. 2012). Most of the proposed experiments are performed using prescribed globally averaged CO2 concentration, not CO2 emissions, allowing participation of both AOGCMs and ESMs. For a given model, the projected climate change is then independent of the strength of its feedbacks associated with the carbon cycle. Concentration–carbon and climate–carbon feedbacks would affect the carbon fluxes between the atmosphere and the underlying land and ocean simulated by an ESM, but these would not affect the atmospheric CO2 concentration as it is prescribed. With an ESM, from the prescribed atmospheric CO2 growth rate and the simulated land and ocean carbon fluxes, one can diagnose the CO2 emissions compatible with the prescribed CO2 concentrations (Matthews 2005, 2006; Jones et al. 2006, 2013). The magnitude of the emissions compatible with the RCP concentrations would be affected by the carbon cycle feedbacks; a model with a large negative climate–carbon cycle feedback would have lower sinks, and hence lower compatible emissions (Jones et al. 2013). Four concentration-driven (C driven) scenarios were proposed for the twenty-first century and beyond, the representative concentration pathways (RCPs) 2.6, 4.5, 6.0, and 8.5 (Moss et al. 2010; van Vuuren et al. 2011; Meinshausen et al. 2011c). Integrated assessment models (IAM) simulated the greenhouse gas and aerosol emissions for these four RCPs scenarios (van Vuuren et al. 2011). These emissions were harmonized with historical estimates and then translated into concentrations using the Model for the Assessment of Greenhouse Gas Induced Climate Change, version 6 (MAGICC6) (Meinshausen et al. 2011a,b,c). MAGICC6 is a simple climate model that also includes a representation of the global carbon cycle and atmospheric chemistry. The carbon cycle is composed of three land carbon pools, an ocean carbon component, and multiple temperature-dependent terrestrial and oceanic carbon fluxes, as well as a parameterization for the CO2 fertilization effect. Through the optimization of several parameters, MAGICC6 can closely reproduce the temporal behavior of higher-complexity physical climate and climate–carbon cycle models [see Meinshausen et al. (2011a) for details on the optimization method]. For the CMIP5 experiments, MAGICC6 used a multimodel average setup of parameters for climate sensitivity, combined with the carbon cycle emulation of the Bern-CC (Joos et al. 2001) taken as the “best estimate” for the carbon cycle behavior. This is essentially because the Bern-CC and its earlier versions have been used for the consolidated concentrations of IPCC SRES scenarios presented in the Third Assessment Report (Prentice et al. 2001; see also appendix II in Houghton et al. 2001).
The CMIP5 protocol recommended that only one scenario, the RCP8.5, be run twice, with CO2 concentration as well as with CO2 emissions as a forcing (Taylor et al. 2012). For these emission-driven simulations, historical CO2 emissions of fossil fuel (Andres et al. 2011) and land use change emissions (Houghton 2010, and updates) as well as twenty-first-century emissions for RCP8.5 (https://tntcat.iiasa.ac.at:8743/RcpDb . This allows a formal comparison between their simulated climate when atmospheric CO2 concentration is prescribed (C-driven runs) and when atmospheric CO2 concentration is calculated from the balance between prescribed CO2 emissions and the simulated atmosphere–land and atmosphere–ocean CO2 fluxes [emission (E)-driven run]. Several modeling groups have performed these two RCP8.5 simulations. Results from 11 ESMs are analyzed here and their main characteristics are listed in Table 1.
Although conceptually simple, the implementation of the E-driven runs was not identical for all models—in particular, with respect to the treatment of the land use change (LUC). Land cover change (LCC) was provided as a standard CMIP5 forcing for all models for the historical period and for each RCP scenario (Hurtt et al. 2006; cmip-pcmdi.llnl.gov/cmip5/forcing.html). This allows ESMs to calculate CO2 emissions that result from the imposed changes in land cover, taking into account that deforestation leads to a direct emission of CO2 as well as indirect emissions due to soil degradation and the later decay of wood products (e.g., McGuire et al. 2001). Conversely, reforestation leads to an initial increase in simulated wood biomass followed by an increase in soil carbon, as the rate of litter fall in forests is higher than for croplands. In addition, tillage in croplands implies that litter and soil decomposition rates are higher over croplands than in forests. Not all models simulate all the LUC-related processes that affect CO2 emissions. Models that do not explicitly calculate LUC emissions can adopt an alternative approach, where LUC CO2 emissions are prescribed as an external forcing in a manner similar to CO2 fossil fuel emissions.
Seven out of the 11 ESMs analyzed here interactively simulated LUC CO2 emissions
Three ESMs (BCC-CSM-1, INM-CM4.0, and MRI-ESM1) prescribed both fossil fuel
3. Simulated atmospheric CO2 and carbon cycle over the historical period
The models simulate the historical changes in atmospheric CO2 and carbon cycle in response to the prescribed anthropogenic perturbation. Fossil fuel emissions combined with the LUC forcing lead to a rapid increase in atmospheric CO2, similar to the observations. However, while the observed atmospheric CO2 reached 379 ppm by 2005, the simulated atmospheric CO2 concentrations range between 358 (MRI-ESM1) and 403 ppm (HadGEM2-ES) for 2005, both underpredicting and overpredicting the historical atmospheric CO2 increase by more than 20% (Fig. 1a; Table 2). Only five models (BCC-CSM-1, CanESM2, INM-CM4.0, MPI-ESM-LR, and NorESM1-ME) are within 10% of the observed CO2 increase. HadGEM2-ES, CESM1-BGC, GFDL-ESM2G, and MIROC-ESM are substantially above the observed concentration by 2005, while IPSL-CM5A-LR and the MRI-ESM1 are significantly below.
Historical atmospheric CO2 (2005), cumulative land and ocean uptake (1850–2005) and average land and ocean uptake (1990–99) simulated by the 11 ESMs compared with the observation-based estimates (with ranges being 68% confidence intervals). Also shown are the multimodel mean and range (1σ).
A priori, reasons for departure from the observed CO2 have to be found in the simulation of the land and ocean CO2 net fluxes [FO and FL in Eq. (1)], assuming here that anthropogenic fossil fuel emissions provided in the CMIP5 protocol represents real-world historical emissions. A brief evaluation of the global atmosphere–land and atmosphere–ocean CO2 fluxes is presented here, and we refer to Anav et al. (2013) for a more in-depth analysis of the carbon cycle in ESMs. The best estimates of the ocean sinks come from both cumulative carbon inventories over the historical period (Sabine et al. 2004, and updates) and from combined oceanic (pCO2 measurements and oceanic inversions) and atmospheric estimates (atmospheric O2 measurements) for the recent decades (Le Quéré et al. 2012). Most ESMs simulate a (1850–2005) cumulative ocean sink ranging between 91 and 155 PgC compared to the observation-derived sink of 141 ± 27 PgC (Table 2). The exceptions are INM-CM4.0, which overestimates the ocean sink by more than a factor of 2 (360 PgC), and CanESM2, which underestimates the ocean sink by about 30%. The behavior of CanESM2 was already reported in Arora et al. (2011), where possible underestimation of the simulated sink was linked to the absence of marginal basins and continental shelves in the model. The large oceanic uptake simulated by INM-CM4.0 is not yet fully understood (E. M. Volodin 2013, personal communication). As shown in Anav et al. (2013), the main reason for discrepancy comes from the tropical ocean, where INMCM4 simulates a strong sink (~1 PgC yr−1) in clear contradiction with the large CO2 outgassing (−1 PgC yr−1) observed. When looking at the decadal mean ocean sink, as estimated in Le Quéré et al. (2012), ESMs generally agree remarkably well with the observation-based oceanic uptake for the last five decades (Fig. 1b), again with the exception of INM-CM4.0, which overestimates the sink from the 1970s onward. CanESM2’s lower-than-average oceanic uptake mainly occurs in the first half of the twentieth century.
The net atmosphere–land CO2 flux
Both NorESM1-ME and CESM1-BGC share the same land surface scheme, the Community Land Model (CLM), and therefore produce similar results in terms of land carbon fluxes. The lower-than-average land sink simulated by these two models is due to the limited response to increasing atmospheric CO2 concentration, as previously reported (Arora et al. 2013; Gillet et al. 2013). CLM accounts for a terrestrial nitrogen cycle (Thornton et al. 2009), a feature not included in any of the other ESMs. Inclusion of the nitrogen cycle generally leads to weaker land carbon uptake estimates (e.g., Zaehle et al. 2010), partly explaining the CLM model behavior. However, the main reason for failing to simulate a significant land sink is the very short residence time of litter and soil carbon in CLM, reducing the lag between the net primary productivity (NPP) increase and the heterotrophic respiration increase—that is, reducing the strength of the land sink (Taylor and Lloyd 1992; Friedlingstein et al. 1995; Thompson et al. 1996). The short soil carbon residence time of CLM was diagnosed through comparison against litterbag measurements (Bonan et al. 2013) as well as comparison of soil carbon spatial distribution against observations (Todd-Brown et al. 2013; Anav et al. 2013), leading to a weak land carbon sink (Keppel-Aleks et al. 2013). Globally, CLM total soil carbon content is less than half of the observations (Todd-Brown et al. 2013; Anav et al. 2013). GFDL-ESM2G also simulates a lower-than-observed
In summary, CESM1-BGC and to a lesser extend GFDL-ESM2G overestimate the atmospheric CO2 growth rate because of a lower-than-observed
4. Twenty-first-century atmospheric CO2 and global temperature change
When forced by CO2 emissions, the 11 ESMs simulate a CO2 concentration trajectory that does not necessarily follow the default CO2 concentration pathway, as provided for CMIP5 by MAGICC6 (Fig. 2a). This is expected since the response of the carbon cycle in CMIP5 ESMs to changes in CO2 and climate need not be same as the one simulated by MAGICC6 in its CMIP5 setting (median CMIP3 AOGCMs for its climate response and Bern-CC for its carbon cycle response) (Meinshausen et al. 2011c). Figure 2a shows the twenty-first-century time evolution of atmospheric CO2 for the 11 ESMs that performed the E-driven RCP8.5 simulations. By 2100, five CMIP5 ESMs (BCC-CSM-1, INM-CM4.0, IPSL-CM5A-LR, MPI-ESM-LR, and NorESM1-ME) simulate CO2 concentrations relatively close (within 5% of the change relative to preindustrial) to the default RCP concentrations that reach 941 ppm by 2100. Five models (CanESM2, CESM1-BGC, GFDL-ESM2G, HadGEM2-ES, MIROC-ESM) simulate much higher CO2 than the default RCP8.5 CO2 concentrations by 2100 and only one—MRI-ESM1—simulates a much lower atmospheric CO2 (Table 3). By 2100, the multimodel average CO2 concentration is 985 ± 97 ppm, with a median of about 970 ppm. Most of the CMIP5 ESMs simulate a larger CO2 when driven by CO2 emissions than the one provided for the concentration-driven scenarios.
Twenty-first-century atmospheric CO2 (2100), global surface warming (2081–99 relative to 1986–2005), cumulative land and ocean uptake (1850–2100) for the E-driven simulations and global surface warming (2081–99 relative to 1986–2005) for the C-driven simulations (where atmospheric CO2 reaches 941 ppm by 2100). Also shown are the multimodel mean and range (1σ) as well as the same quantities simulated by MAGICC6 in its reference setting.
It is worth noting that by 2005, these five models already overestimated the CO2 concentration, while MRI-ESM1 already severely underestimated it, thus potentially pointing to a persistent bias in these six ESMs.
By 2100, the largest CO2 concentration is obtained with MIROC-ESM, reaching 1149 ppmv by 2100—more than 200 ppm higher than the amount of CO2 from MAGICC6 used in the concentration-driven simulations (see Table 2). MRI-ESM1 simulates a CO2 of 794 ppm by 2100—150 ppm lower than the RCP8.5 default value. This model severely underestimates the present-day CO2, with a 2005 concentration of 358 ppm—more than 20 ppm below the observed value, potentially indicating an issue in the protocol followed by this model.
In general there is a clear correlation between the models’ bias in atmospheric CO2 by 2005 and the models’ departure from the MAGICC6 CO2 by 2100 (Fig. 3). However, it should be noted that a model match with the present-day atmospheric CO2 does not imply that the model correctly simulates the land and the ocean carbon uptake. Indeed, INM-CM4.0 perfectly simulates the atmospheric CO2 concentration by 2005, but because of a stronger-than-observed ocean sink combined with a weaker-than-observed land sink. The same applies to BCC-CSM-1 with, in that case, a weak ocean sink combined with a strong land sink.
The larger CO2 concentration simulated in the emission-driven simulations induces an additional radiative forcing (multimodel average is 0.25 ± 0.5 W m−2). The simulated warming in the E-driven run is therefore generally larger than the one simulated in the C-driven runs of the same ESMs (Fig. 2b). For the C-driven simulations, the global surface temperature change (2081–2100 average relative to the 1986–2005 average) ranges between 2.6° and 4.7°C, with a multimodel average of 3.7° ± 0.7°C (Table 2). The E-driven simulations give a range of 2.5°–5.6°C, with a multimodel average of 3.9° ± 0.9°C—that is, 0.2°C larger than for the concentration-driven simulations. Three models—CanESM2, CESM1-BGC, and MIROC-ESM—have a strong warming amplification in the E-driven simulations, with an additional warming of 0.5°, 0.5° and 0.9°C, respectively. HadGEM2-ES and MRI-ESM1 are the exceptions, both with a warming 0.4°C lower in the E-driven run than in the C-driven run. For MRI-ESM1, this is directly due to the lower simulated atmospheric CO2 in the emission-driven run. We note that HadGEM2-ES already overestimates present-day CO2 by about 25 ppm, partly explaining this unexpected behavior, as the warming shown here is only the increase above current warming levels (1986–2005), not since preindustrial times.
To put the CMIP5 model range into perspective of the IPCC AR4 range (Meehl et al. 2007), we used a large ensemble of MAGICC6 runs to emulate the CO2 and global temperature response one would get for the RCP8.5 scenario if generated by the IPCC AR4 models’ runs (Figs. 2c and 2d). MAGICC6 was run by a uniform sampling of the climate sensitivity uncertainty taken from 19 CMIP3 models and the carbon cycle feedbacks uncertainty taken from 10 C4MIP models, generating 190 model simulations (Meinshausen et al. 2011a). At first glance, the range of atmospheric CO2 from the CMIP5 ESMs and from the MAGICC6 emulation of the CMIP3/C4MIP models is quite similar (Figs. 2a and 2c)—in particular, both sets give a comparable upper estimate of the atmospheric CO2 concentration, about 1150 ppm by 2100. However, the comparison is not straightforward for the lower end of the projections. As already noted above, most ESMs simulate larger CO2 concentrations than the MAGICC baseline estimate (red line in Figs. 2a and 2c). For 2100, the range of CO2 concentrations is 794–1149 ppm for the 11 CMIP5 ESMs analyzed here, while the range (90% probability) for the CMIP3/C4MIP emulation with MAGICC6 is 811–1170 ppm. As discussed above, the lower range of the CMIP5 ESMs is due to one single model, MRI-ESM1, which already severely underestimates the present-day atmospheric CO2 concentration. Not including this model would mean that the lower end of the MAGICC6 range is significantly lower than the lower end of the CMIP5 ESMs.
The warming ranges simulated by the CMIP5 ESMs and by the CMIP3/C4MIP model emulations are quite similar (Figs. 2b and 2d). The first set of models displays a full range of 2.5°–5.6°C, while the latter set has a 90% probability range of 2.9°–5.9°C.
5. Twenty-first-century land and ocean carbon cycle
To further understand the difference in simulated atmospheric CO2 over the twenty-first century, we analyzed the carbon budget simulated by the models, as already done for the historical period. In the E-driven runs, the ESMs simulate the atmospheric CO2 concentration as the residual of the prescribed anthropogenic emissions minus the sum of the land and ocean carbon uptakes—these latter two fluxes being interactively computed by the land and ocean biogeochemical components of the ESMs. Figure 4 shows the cumulative land and ocean carbon uptakes simulated by the CMIP5 ESMs. Any difference in simulated atmospheric CO2 comes from differences in the land or ocean uptakes.
The models show a large range of future carbon uptake, both for the land and for the ocean (Figs. 4a and 4b). However, for the ocean, 10 out of the 11 models have a cumulative oceanic uptake ranging between 412 and 649 PgC by 2100, the exception being INM-CM4.0 with an oceanic uptake of 861 PgC. As discussed in the historical section, the reasons for this large simulated uptake are unknown. The simulated land carbon fluxes show a much larger range, from a cumulative source of 165 PgC to a cumulative sink of 758 PgC. Eight models simulate that the land acts as a carbon sink over the full period. Land is simulated to be a carbon source by two models, CESM1-BGC and NorESM1-ME, both sharing the same land carbon cycle model, and by MIROC-ESM. The large uncertainty in the atmosphere–land CO2 fluxes is partly due to not all models including land use changes in their calculations of their net land–atmosphere carbon flux. Indeed, MRI-ESM1 and to a lesser extent BCC-CSM1 do not include land use change. Hence, these models only simulate
The MAGICC6 emulations of the wide range of CMIP3 and C4MIP model simulations show a similar response, with a much larger spread for the land carbon fluxes than for the ocean carbon fluxes, with a 90% probability range of 446–897 PgC for the ocean carbon sink and −373 to 657 for the land carbon sink. In the MAGICC6 simulations, land use change fluxes are always accounted for, in a consistent manner across all models, further indicating that the large spread of the land carbon cycle is due to the representation of the natural biogeochemical cycle, not the implementation of the land use perturbation.
Annual fluxes obviously show a similar behavior (Figs. 4c and 4d), with CMIP5 ESMs simulating the land being by the end of the twenty-first century either a net sink of up to 4 PgC yr−1 (although of decreasing amplitude for all models) or a net source of 6 PgC yr−1 for the MIROC-ESM model. On the ocean side, all models simulate a continuous sink across the twenty-first century, reaching 4.5–6 PgC yr−1 by the end of the century.
6. Discussion
CMIP5 earth system models still simulate a large uncertainty in CO2 projection, with more than 350-ppm uncertainty of projected CO2 concentrations by 2100 for the RCP8.5 scenario. This large range is mainly due to the uncertainty in the land carbon cycle projections, where models do not even agree on the sign of the atmosphere–land CO2 flux by the end of the century. Whether the land would be a source or a sink of carbon by 2100 under the RCP8.5 is unclear. A similar conclusion was reached in the C4MIP analysis at the time of the IPCC AR4, with different models and a different emissions scenario (Friedlingstein et al. 2006).
However, here we are able to attribute some of the large spread to differences in model setup and their complexity. First, we show that out of the 11 models considered, 8 include the impact of land cover changes on simulated atmosphere–land CO2 fluxes, while the remaining 3 use prescribed LUC emissions as an external forcing. This artificially creates a large spread in the simulated atmosphere–land CO2 flux. Leaving out the models that prescribe LUC emissions externally, such that the effect of land use changes is neglected in their modeled atmosphere–land CO2 flux, the range is reduced from [−173 to 758] to [−173 to 352]. Further, two of the three models that simulate a land source—CESM1-BGC and NorESM1-ME—share the same land surface scheme (CLM). As mentioned before, CLM has a very weak land response to CO2, because of a too-fast litter and soil carbon turnover time, combined with a nitrogen cycle that dampens the response to CO2 (Thornton et al. 2009; Zaehle et al. 2010). Hence, carbon loss from LUC and warming are expected to be larger than carbon gains because of CO2 fertilization for CESM1-BGC and NorESM1-ME. MIROC-ESM, the third model that simulates a land source by 2100, has a relatively weak land carbon cycle response to CO2, but a very large land carbon cycle response to climate as reported before (Hajima et al. 2012; Arora et al. 2013). Arora et al. (2013) found that in the 1% yr−1 increasing CO2 simulations, MIROC-ESM has the strongest land carbon–climate feedback among the nine ESMs compared in that study.
It is worth noting that as every ESM simulates its own climate, the model spread in land carbon response to climate is also partly due to the model-specific spatial patterns of changes in key climate drivers such as temperature and precipitation (Knutti and Sedláček 2012).
We analyzed the performance of the CMIP5 ESMs over the historical period in terms of simulated atmospheric CO2, land, and carbon uptakes (Table 2). Although this cannot directly be used as a constraint, there is a clear correlation between CO2 simulated by 2005 and by 2100. The models with a lower-than-observed present-day CO2 have a lower-than-average CO2 by 2100, and likewise, the models with higher-than-observed CO2 by 2005 have high CO2 by 2100, indicating that present-day observations are key constraints for the carbon cycle of ESMs. However, the models’ order within these two groups is not conserved across time. Furthermore, when looking at the present-day carbon budget as simulated by the ESMs (Table 2), there is no clear relationship between the realism of the present-day land or ocean global uptake and the twenty-first-century projections, meaning that the correlation observed for CO2 might be accidental (e.g., compensation of errors between land and ocean sinks). Several model evaluation activities have been initiated over the last couple of years (e.g., Randerson et al. 2009; Cadule et al. 2010; Blyth et al. 2011; Anav et al. 2013; Cox et al. 2013), helping to gain confidence in some aspects of the simulated carbon cycle, but not yet leading to a significant reduction in uncertainty for the CMIP5 exercise. From the analysis here, it seems clear that most of the ESMs were not fully evaluated in terms of their carbon cycle response before performing and submitting the CMIP5 simulations. This might also be a side effect of the CMIP5 protocol (Taylor et al. 2012), where the core of the simulations was with prescribed CO2 concentration, leaving the carbon cycle as a nonessential element for climate simulations.
Our analyses suggest that, for the RCP8.5 scenario, the CMIP5 ESMs produce, on average, a slightly higher CO2 concentration compared to the default RCP8.5 CO2 concentrations and hence a slightly larger warming. This is similar to the outcome of the CMIP3 exercise where the Bern-CC CO2 concentrations were chosen as a default for most CMIP3 models in the concentration-driven runs, but the C4MIP intercomparison suggested that this choice was producing slightly below-average CO2 concentrations. This is somewhat replicated this time for CMIP5, given that the carbon cycle of MAGICC6 was calibrated to BERN-CC in order to produce the GHG concentrations of the RCPs (Meinshausen et al. 2011c). In other words, the default dataset implied again slightly lower CO2 concentrations for the concentration-driven runs than what CMIP5 ESMs suggest for emission-driven runs.
However, we also find that most of the models that simulate high-end CO2 in 2100 overestimate the present-day CO2 concentration, suggesting that either these models underestimate the land and/or ocean carbon sinks or that the emissions used to drive the ESMs are slightly overestimated, casting some doubts on the added realism of emission-driven simulations when compared to concentration-driven simulations.
Temperature projected by the 11 ESMs driven by CO2 emissions is on the average higher than when driven by CO2 concentration (Fig. 5). When compared to the temperature change simulated by all RCP8.5 C-driven simulations available (not just the ones from the 11 ESMs used here), we find that the C-driven runs from the ESMs analyzed here produce a very similar warming than the full CMIP5 database (Knutti and Sedláček 2012). When attempting to estimate the projected warming and uncertainty, from a given emission pathway, our study suggests that, for the RCP8.5 emission scenario, the best estimates of warming could be about 0.2°C higher than the estimate based solely on CMIP5 concentration-driven simulations. Whether this would also apply to the other RCP scenarios is unclear. Jones et al. (2013) found that, for both the RCP6.0 and RCP8.5, the ESMs derived compatible emissions were, on the average, lower than the one estimated by the integrated assessment models, consistent with our estimate that the ESMs simulate larger CO2 when using these prescribed emissions. However, this was not the case for the RCP2.6 and RCP4.5, where Jones et al. (2013) found no significant difference in terms of derived emissions.
Finally, while for the SRES scenarios the concentration-driven experimental setup was often seen as a compromise (as most models could then, as today, not be driven by CO2 emissions), the CMIP5 exercise embraced the philosophy of concentrations-driven runs more consistently, starting with representative “concentration” pathways. Thus, as long as the CMIP5 climate projections are clearly communicated as referring to a specific evolution of atmospheric CO2 concentrations, non-CO2 concentrations, and aerosol abundances, there is no necessity to apply any adjustments because of more developed insights in regard to concentration–carbon cycle or climate–carbon cycle feedbacks. There is, however, the new opportunity arising from these CMIP5 ESM simulations to quantify the “allowable” carbon space—that is, the cumulative emissions that are in line with one or the other concentration pathway.
Acknowledgments
We acknowledge the World Climate Research Programme’s Working Group on Coupled Modelling, which is responsible for CMIP, and we thank the climate modeling groups (listed in Table 1 of this paper) for producing and making available their model output. For CMIP, the U.S. Department of Energy’s Program for Climate Model Diagnosis and Intercomparison provides coordinating support and led development of software infrastructure in partnership with the Global Organization for Earth System Science Portals. PF and AA acknowledge the GREENCYCLESII, COMBINE, and EMBRACE EU/FP7 projects. CDJ and SKL were supported by the Joint DECC/Defra Met Office Hadley Centre Climate Programme (GA01101).
REFERENCES
Adachi, Y., and Coauthors, 2013: Basic performance of a new Earth System Model of the Meteorological Research Institute (MRI-ESM1). Pap. Meteor. Geophys., in press.
Anav, A., and Coauthors, 2013: Evaluating the land and ocean components of the global carbon cycle in the CMIP5 earth system models. J. Climate, 26, 6801–6843.
Andres, R. J., J. S. Gregg, L. Losey, G. Marland, and T. A. Boden, 2011: Monthly, global emissions of carbon dioxide from fossil fuel consumption. Tellus,63B, 309–327, doi:10.1111/j.1600-0889.2011.00530.x.
Arora, V. K., and G. J. Boer, 2010: Uncertainties in the 20th century carbon budget associated with land use change. Global Change Biol., 16, 3327–3348.
Arora, V. K., and Coauthors, 2011: Carbon emission limits required to satisfy future representative concentration pathways of greenhouse gases. Geophys. Res. Lett., 38, L05805, doi:10.1029/2010GL046270.
Arora, V. K., and Coauthors, 2013: Carbon–concentration and carbon–climate feedbacks in CMIP5 earth system models. J. Climate, 26, 5289–5314.
Blyth, E., D. B. Clark, R. Ellis, C. Huntingford, S. Los, M. Pryor, M. Best, and S. Sitch, 2011: A comprehensive set of benchmark tests for a land surface model of simultaneous fluxes of water and carbon at both the global and seasonal scale. Geosci. Model Dev., 4, 255–269.
Bonan, G. B., M. D. Hartman, W. J. Parton, and W. R. Wieder, 2013: Evaluating litter decomposition in earth system models with long-term litterbag experiments: An example using the Community Land Model version 4 (CLM4). Global Change Biol., 19, 957–974, doi:10.1111/gcb.12031.
Bony, S., and Coauthors, 2006: How well do we understand and evaluate climate change feedback processes? J. Climate, 19, 3445–3482.
Cadule, P., P. Friedlingstein, L. Bopp, S. Sitch, C. D. Jones, P. Ciais, S. L. Piao, and P. Peylin, 2010: Benchmarking coupled climate-carbon models against long-term atmospheric CO2 measurements. Global Biogeochem. Cycles, 24, GB2016, doi:10.1029/2009GB003556.
Collins, W. J., and Coauthors, 2011: Development and evaluation of an earth-system model—HadGEM2. Geosci. Model Dev., 4, 1051–1075.
Cox, P. M., D. Pearson, B. B. Booth, P. Friedlingstein, C. Huntingford, C. D. Jones, and C. M. Luke, 2013: Sensitivity of tropical carbon to climate change constrained by carbon dioxide variability. Nature, 494, 341–344, doi:10.1038/nature11882.
Cramer, W., and Coauthors, 2001: Global response of terrestrial ecosystem structure and function to CO2 and climate change: Results from six dynamic global vegetation models. Global Change Biol., 7, 357–373.
Denman, K. L., and Coauthors, 2007: Coupling between changes in the climate system and biogeochemistry. Climate Change 2007: The Physical Science Basis, S. Solomon et al., Eds., Cambridge University Press, 499–587.
Dufresne, J.-L., and Coauthors, 2013: Climate change projections using the IPSL-CM5 earth system model: From CMIP3 to CMIP5. Climate Dyn., 40, 2123–2165.
Dunne, J., and Coauthors, 2013: GFDL’s ESM2 global coupled climate–carbon earth system models. Part II: Carbon system formulation and baseline simulation characteristics. J. Climate,26, 2247–2267.
Forster, P. M. D., and K. E. Taylor, 2006: Climate forcings and climate sensitivities diagnosed from coupled climate model integrations. J. Climate, 19, 6181–6194.
Friedlingstein, P., I. Y. Fung, E. A. Holland, J. G. John, G. P. Brasseur, D. J. Erickson, and D. S. Schimel, 1995: On the contribution of CO2 fertilization to the missing biospheric sink. Global Biogeochem. Cycles, 9, 541–556.
Friedlingstein, P., and Coauthors, 2006: Climate–carbon cycle feedback analysis: Results from the C4MIP model intercomparison. J. Climate, 19, 3337–3353.
Friedlingstein, P., and Coauthors, 2010: Update on CO2 emissions. Nat. Geosci., 3, 811–812.
Gillet, N. P., V. K. Arora, D. Matthews, and M. R. Allen, 2013: Constraining the ratio of global warming to cumulative CO2 emissions using CMIP5 simulations. J. Climate, 26, 6844–6858.
Gregory, J. M., C. D. Jones, P. Cadule, and P. Friedlingstein, 2009: Quantifying carbon cycle feedbacks. J. Climate, 22, 5232–5250.
Hajima, T., T. Ise, K. Tachiiri, E. Kato, S. Watanabe, and M. Kawamiya, 2012: Climate change, allowable emission, and earth system response to representative concentration pathway scenarios. J. Meteor. Soc. Japan, 90, 417–433.
Hawkins, E., and R. Sutton, 2009: The potential to narrow uncertainty in regional climate predictions. Bull. Amer. Meteor. Soc., 90, 1095–1107.
Hibbard, K. A., G. A. Meehl, P. Cox, and P. Friedlingstein, 2007: A strategy for climate change stabilization experiments. Eos, Trans. Amer. Geophys. Union, 88, 217–221, doi:10.1029/2007EO200002.
Houghton, J. T., Y. Ding, D. J. Griggs, M. Noguer, P. J. van der Linden, X. Dai, K. Maskell, and C. A. Johnson, Eds., 2001: Climate Change 2001: The Scientific Basis. Cambridge University Press, 881 pp.
Houghton, R. A., 2010: How well do we know the flux of CO2 from land-use change? Tellus,62B, 337–351, doi:10.1111/j.1600-0889.2010.00473.x.
Hurtt, G. C., S. Frolking, M. G. Fearon, B. Moore, E. Shevliakova, S. Malyshev, S. W. Pacala, and R. A. Houghton, 2006: The underpinnings of land-use history: Three centuries of global gridded land-use transitions, wood-harvest activity, and resulting secondary lands. Global Change Biol., 12, 1208–1229, doi:10.1111/j.1365-2486.2006.01150.x.
Ilyina, T., K. D. Six, J. Segschneider, E. Maier-Reimer, H. Li, and I. Núñez-Riboni, 2013: Global ocean biogeochemistry model HAMOCC: Model architecture and performance as component of the MPI-Earth System Model in different CMIP5 experimental realizations. J. Adv. Model. Earth Syst., 5, 287–315, doi:10.1029/2012MS000178.
Jones, C. D., P. M. Cox, and C. Huntingford, 2006: Climate-carbon cycle feedbacks under stabilization: Uncertainty and observational constraints. Tellus, 58B, 603–613.
Jones, C. J., and Coauthors, 2013: Twenty-first-century compatible CO2 emissions and airborne fraction simulated by CMIP5 earth system models under four representative concentration pathways. J. Climate,26, 4398–4413.
Joos, F., I. C. Prentice, S. Sitch, R. Meyer, G. Hooss, G.-K. Plattner, S. Gerber, and K. Hasselmann, 2001: Global warming feedbacks on terrestrial carbon uptake under the Intergovernmental Panel on Climate Change (IPCC) emission scenarios. Global Biogeochem. Cycles, 15, 891–907.
Keppel-Aleks, G., and Coauthors, 2013: Atmospheric carbon dioxide variability in the Community Earth System Model: Evaluation and transient dynamics during the twentieth and twenty-first centuries. J. Climate,26, 4447–4475.
Knutti, R., and J. Sedláček, 2012: Robustness and uncertainties in the new CMIP5 climate model projections. Nat. Climate Change, 3, 369–373, doi:10.1038/nclimate1716.
Knutti, R., and Coauthors, 2008: A review of uncertainties in global temperature projections over the twenty‐first century. J. Climate, 21, 2651–2663.
Le Quéré, C., and Coauthors, 2009: Trends in the sources and sinks of carbon dioxide. Nat. Geosci., 2, 831–836, doi:10.1038/ngeo689.
Le Quéré, C., and Coauthors, 2012: The global carbon budget 1959–2011. Earth Syst. Sci. Data Discuss., 5, 1107–1157.
Long, M. C., K. Lindsay, S. Peacock, J. K. Moore, and S. C. Doney, 2013: Twentieth-century oceanic carbon uptake and storage in CESM1(BGC). J. Climate, 26, 6775–6800.
Matthews, H. D., 2005: Decrease of emissions required to stabilize atmospheric CO2 due to positive carbon cycle–climate feedbacks. Geophys. Res. Lett., 32, L21707, doi:10.1029/2005GL023435.
Matthews, H. D., 2006: Emissions targets for CO2 stabilization as modified by carbon cycle feedbacks. Tellus, 58B, 591–602.
McGuire, A. D., and Coauthors, 2001: Carbon balance of the terrestrial biosphere in the twentieth century: Analyses of CO2, climate and land use effects with four process-based ecosystem models. Global Biogeochem. Cycles, 15, 183–206.
Meehl, G. A., and Coauthors, 2007: Global climate projections. Climate Change 2007: The Physical Science Basis, S. Solomon et al., Eds., Cambridge University Press, 747–845.
Meinshausen, M., S. C. B. Raper, and T. M. L. Wigley, 2011a: Emulating coupled atmosphere-ocean and carbon cycle models with a simpler model, MAGICC6—Part 1: Model description and calibration. Atmos. Chem. Phys., 11, 1417–1456.
Meinshausen, M., T. M. L. Wigley, and S. C. B. Raper, 2011b: Emulating atmosphere-ocean and carbon cycle models with a simpler model, MAGICC6—Part 2: Applications. Atmos. Chem. Phys., 11, 1457–1471.
Meinshausen, M., and Coauthors, 2011c: The RCP greenhouse gas concentrations and their extension from 1765 to 2300. Climatic Change, 109, 213–241, doi:10.1007/s10584-011-0156-z.
Moss, R. H., and Coauthors, 2010: The next generation of scenarios for climate change research and assessment. Nature, 463, 747–756.
Nakicenovic, N., and R. Swart, Eds., 2000: Special Report on Emissions Scenarios. Cambridge University Press, 599 pp.
Orr, J. C., and Coauthors, 2001: Estimates of anthropogenic carbon uptake from four three-dimensional global ocean models. Global Biogeochem. Cycles, 15, 43–60.
Peters, G. P., G. Marland, C. Le Quéré, T. Boden, J. G. Canadell, and M. R. Raupach, 2012: Rapid growth in CO2 emissions after the 2008–2009 global financial crisis. Nat. Climate Change,2, 2–4, doi:10.1038/nclimate1332.
Prentice, I. C., and Coauthors, 2001: The carbon cycle and atmospheric carbon dioxide. Climate Change 2001: The Scientific Basis, J. T. Houghton et al., Eds., Cambridge University Press, 183–238.
Randerson, J. T., and Coauthors, 2009: Systematic assessment of terrestrial biogeochemistry in coupled climate–carbon models. Global Change Biol., 15, 2462–2484, doi:10.1111/j.1365-2486.2009.01912.x.
Sabine, C. L., and Coauthors, 2004: The oceanic sink for anthropogenic CO2. Science, 305,367–371.
Shevliakova, E., and Coauthors, 2009: Carbon cycling under 300 years of land use change: Importance of the secondary vegetation sink. Global Biogeochem. Cycles, 23, GB2022, doi:10.1029/2007GB003176.
Sitch, S., and Coauthors, 2008: Evaluation of the terrestrial carbon cycle, future plant geography, and climate-carbon cycle feedbacks using five dynamic global vegetation models (DGVMs). Global Change Biol., 14, 2015–2039, doi:10.1111/j.1365-2486.2008.01626.x.
Solomon, S., D. Qin, M. Manning, Z. Chen, M. Marquis, K. Averyt, M. Tignor, and H. L. Miller Jr., Eds., 2007: Climate Change 2007: The Physical Science Basis. Cambridge University Press, 996 pp.
Taylor J. A., and J. Lloyd, 1992: Sources and sinks of atmospheric CO2. Aust. J. Bot.,40, 407–418.
Taylor, K. E., R. J. Stouffer, and G. A. Meehl, 2012: An overview of CMIP5 and the experiment design. Bull. Amer. Meteor. Soc., 93, 485–498.
Tebaldi, C., and R. Knutti, 2007: The use of the multi-model ensemble in probabilistic climate projections. Philos. Trans. Roy. Soc. London, A365, 2053–2075, doi:10.1098/rsta.2007.2076.
Thompson, M. V., J. T. Randerson, C. M. Malmström, and C. B. Field, 1996: Change in net primary production and heterotrophic respiration: How much is necessary to sustain the terrestrial carbon sink? Global Biogeochem. Cycles, 10, 711–726.
Thornton, P., and Coauthors, 2009: Carbon-nitrogen interactions regulate climate-carbon cycle feedbacks: Results from an atmosphere-ocean general circulation model. Biogeosciences, 6, 2099–2120, doi:10.5194/bg-6-2099-2009.
Tjiputra, J. F., C. Roelandt, M. Bentsen, D. M. Lawrence, T. Lorentzen, J. Schwinger, Ø. Seland, and C. Heinze, 2012: Evaluation of the carbon cycle components in the Norwegian Earth System Model (NorESM). Geosci. Model Dev. Discuss., 5, 3035–3087.
Todd-Brown, K. E. O., J. T. Randerson, W. M. Post, F. M. Hoffman, C. Tarnocai, E. A. G. Schuur, and S. D. Allison, 2013: Causes of variation in soil carbon predictions from CMIP5 earth system models and comparison with observations. Biogeosciences, 10, 1717–1736, doi:10.5194/bg-10-1717-2013.
van Vuuren, D. P., and Coauthors, 2011: The representative concentration pathways: An overview. Climatic Change, 109, 5–31, doi:10.1007/s10584-011-0148-z.
VEMAP members, 1995: Vegetation/Ecosystem Modeling and Analysis Project: Comparing biogeography and biogeochemistry models in a continental-scale study of terrestrial ecosystem responses to climate change and CO2 doubling. Global Biogeochem. Cycles, 9, 407–437.
Volodin, E. M., N. A. Dianskii, and A. V. Gusev, 2010: Simulating present-day climate with the INMCM4.0 coupled model of the atmospheric and oceanic general circulations. Izv. Atmos. Oceanic Phys., 46, 414–431.
Watanabe, S., and Coauthors, 2011: MIROC-ESM 2010: Model description and basic results of CMIP5-20c3m experiments. Geosci. Model Dev., 4, 845–872.
Wu, T., and Coauthors, 2010: The Beijing Climate Center atmospheric general circulation model: Description and its performance for the present-day climate. Climate Dyn., 34, 123–147, doi:10.1007/s00382-008-0487-2.
Xin, X., L. Zhang, J. Zhang, T. Wu, and Y. Fang, 2013a: Climate change projections over East Asia with BCC_CSM1.1 climate model under RCP scenarios. J. Meteor. Soc. Japan, 91, 413–429.
Xin, X.-G., T.-W. Wu, J.-L. Li, Z.-Z. Wang, W.-P. Li, and F.-H. Wu, 2013b: How well does BCC_CSM1.1 reproduce the 20th century climate change over China? Atmos. Oceanic Sci. Lett., 6, 21–26.
Zaehle, S., P. Friedlingstein, and A. D. Friend, 2010: Terrestrial nitrogen feedbacks may accelerate future climate change. Geophys. Res. Lett., 37, L01401, doi:10.1029/2009GL041345.