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- ItemHistorical greenhouse gas concentrations for climate modelling (CMIP6)(München : European Geopyhsical Union, 2017) Meinshausen, Malte; Vogel, Elisabeth; Nauels, Alexander; Lorbacher, Katja; Meinshausen, Nicolai; Etheridge, David M.; Fraser, Paul J.; Montzka, Stephen A.; Rayner, Peter J.; Trudinger, Cathy M.; Krummel, Paul B.; Beyerle, Urs; Canadell, Josep G.; Daniel, John S.; Enting, Ian G.; Law, Rachel M. Law; Lunder, Chris R.; O'Doherty, Simon; Prinn, Ron G.; Reimann, Stefan; Rubino, Mauro; Velders, Guus J.M.; Vollmer, Martin K.; Wang, Ray H.J.; Weiss, RayAtmospheric greenhouse gas (GHG) concentrations are at unprecedented, record-high levels compared to the last 800000 years. Those elevated GHG concentrations warm the planet and – partially offset by net cooling effects by aerosols – are largely responsible for the observed warming over the past 150 years. An accurate representation of GHG concentrations is hence important to understand and model recent climate change. So far, community efforts to create composite datasets of GHG concentrations with seasonal and latitudinal information have focused on marine boundary layer conditions and recent trends since the 1980s. Here, we provide consolidated datasets of historical atmospheric concentrations (mole fractions) of 43 GHGs to be used in the Climate Model Intercomparison Project – Phase 6 (CMIP6) experiments. The presented datasets are based on AGAGE and NOAA networks, firn and ice core data, and archived air data, and a large set of published studies. In contrast to previous intercomparisons, the new datasets are latitudinally resolved and include seasonality. We focus on the period 1850–2014 for historical CMIP6 runs, but data are also provided for the last 2000 years. We provide consolidated datasets in various spatiotemporal resolutions for carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O), as well as 40 other GHGs, namely 17 ozone-depleting substances, 11 hydrofluorocarbons (HFCs), 9 perfluorocarbons (PFCs), sulfur hexafluoride (SF6), nitrogen trifluoride (NF3) and sulfuryl fluoride (SO2F2). In addition, we provide three equivalence species that aggregate concentrations of GHGs other than CO2, CH4 and N2O, weighted by their radiative forcing efficiencies. For the year 1850, which is used for pre-industrial control runs, we estimate annual global-mean surface concentrations of CO2 at 284.3ppm, CH4 at 808.2ppb and N2O at 273.0ppb. The data are available at https://esgf-node.llnl.gov/search/input4mips/ and http://www.climatecollege.unimelb.edu.au/cmip6. While the minimum CMIP6 recommendation is to use the global- and annual-mean time series, modelling groups can also choose our monthly and latitudinally resolved concentrations, which imply a stronger radiative forcing in the Northern Hemisphere winter (due to the latitudinal gradient and seasonality).
- ItemThe role of orbital forcing, carbon dioxide and regolith in 100 kyr glacial cycles(München : European Geopyhsical Union, 2011) Ganopolski, A.; Calov, R.The origin of the 100 kyr cyclicity, which dominates ice volume variations and other climate records over the past million years, remains debatable. Here, using a comprehensive Earth system model of intermediate complexity, we demonstrate that both strong 100 kyr periodicity in the ice volume variations and the timing of glacial terminations during past 800 kyr can be successfully simulated as direct, strongly nonlinear responses of the climate-cryosphere system to orbital forcing alone, if the atmospheric CO2 concentration stays below its typical interglacial value. The existence of long glacial cycles is primarily attributed to the North American ice sheet and requires the presence of a large continental area with exposed rocks. We show that the sharp, 100 kyr peak in the power spectrum of ice volume results from the long glacial cycles being synchronized with the Earth's orbital eccentricity. Although 100 kyr cyclicity can be simulated with a constant CO2 concentration, temporal variability in the CO2 concentration plays an important role in the amplification of the 100 kyr cycles.
- ItemA model-based constraint on CO2 fertilisation(München : European Geopyhsical Union, 2013) Holden, P.B.; Edwards, N.R.; Gerten, D.; Schaphoff, S.We derive a constraint on the strength of CO2 fertilisation of the terrestrial biosphere through a "top-down" approach, calibrating Earth system model parameters constrained by the post-industrial increase of atmospheric CO2 concentration. We derive a probabilistic prediction for the globally averaged strength of CO2 fertilisation in nature, for the period 1850 to 2000 AD, implicitly net of other limiting factors such as nutrient availability. The approach yields an estimate that is independent of CO2 enrichment experiments. To achieve this, an essential requirement was the incorporation of a land use change (LUC) scheme into the GENIE Earth system model. Using output from a 671-member ensemble of transient GENIE simulations, we build an emulator of the change in atmospheric CO2 concentration change since the preindustrial period. We use this emulator to sample the 28-dimensional input parameter space. A Bayesian calibration of the emulator output suggests that the increase in gross primary productivity (GPP) in response to a doubling of CO2 from preindustrial values is very likely (90% confidence) to exceed 20%, with a most likely value of 40–60%. It is important to note that we do not represent all of the possible contributing mechanisms to the terrestrial sink. The missing processes are subsumed into our calibration of CO2 fertilisation, which therefore represents the combined effect of CO2 fertilisation and additional missing processes. If the missing processes are a net sink then our estimate represents an upper bound. We derive calibrated estimates of carbon fluxes that are consistent with existing estimates. The present-day land–atmosphere flux (1990–2000) is estimated at −0.7 GTC yr−1 (likely, 66% confidence, in the range 0.4 to −1.7 GTC yr−1). The present-day ocean–atmosphere flux (1990–2000) is estimated to be −2.3 GTC yr−1 (likely in the range −1.8 to −2.7 GTC yr−1). We estimate cumulative net land emissions over the post-industrial period (land use change emissions net of the CO2 fertilisation and climate sinks) to be 66 GTC, likely to lie in the range 0 to 128 GTC.