Carbon dioxide and climate impulse response functions for the computation of greenhouse gas metrics: a multi-model analysis
Autor: | K. M. Strassmann, Katsumasa Tanaka, Thomas Kleinen, C. D. Jones, Axel Timmermann, Philip B. Holden, Gary Shaffer, Malte Meinshausen, Gian-Kasper Plattner, Michael Eby, Fortunat Joos, Marco Steinacher, Neil R. Edwards, Andy Reisinger, Jan S. Fuglestvedt, Andrew J. Weaver, Tobias Friedrich, W. von Bloh, Joachim Segschneider, Paul R. Halloran, Eleanor J. Burke, Thomas L. Frölicher, Raphael Roth, Glen P. Peters, Fred T. Mackenzie, Victor Brovkin, Katsumi Matsumoto, Ian G. Enting |
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Rok vydání: | 2013 |
Předmět: |
Atmospheric Science
Global temperature 010504 meteorology & atmospheric sciences 530 Physics Ocean acidification 010501 environmental sciences 01 natural sciences 7. Clean energy lcsh:QC1-999 lcsh:Chemistry Atmosphere chemistry.chemical_compound lcsh:QD1-999 chemistry 13. Climate action Climatology Greenhouse gas Carbon dioxide Environmental science Ocean heat content lcsh:Physics Sea level Impulse response 550 Earth sciences & geology 0105 earth and related environmental sciences |
Zdroj: | Atmospheric Chemistry and Physics Joos, Fortunat; Roth, Raphael; Fuglestvedt, J. S.; Peters, G. P.; Enting, I. G.; von Bloh, W.; Brovkin, V.; Burke, E. J.; Eby, M.; Edwards, N. R.; Friedrich, T.; Frölicher, Thomas; Halloran, P. R.; Holden, P. B.; Jones, C.; Kleinen, T.; Mackenzie, F. T.; Matsumoto, K.; Meinshausen, M.; Plattner, Gian-Kasper; ... (2013). Carbon dioxide and climate impulse response functions for the computation of greenhouse gas metrics: a multi-model analysis. Atmospheric chemistry and physics, 13(5), pp. 2793-2825. European Geosciences Union 10.5194/acp-13-2793-2013 Atmospheric Chemistry and Physics, 13 (5) Atmospheric Chemistry and Physics, 12 (8) Atmospheric Chemistry and Physics, Vol 13, Iss 5, Pp 2793-2825 (2013) Atmospheric Chemistry and Physics Discussions |
ISSN: | 1680-7324 |
DOI: | 10.5194/acp-13-2793-2013 |
Popis: | The responses of carbon dioxide (CO2) and other climate variables to an emission pulse of CO2 into the atmosphere are often used to compute the Global Warming Potential (GWP) and Global Temperature change Potential (GTP), to characterize the response timescales of Earth System models, and to build reduced-form models. In this carbon cycle-climate model intercomparison project, which spans the full model hierarchy, we quantify responses to emission pulses of different magnitudes injected under different conditions. The CO2 response shows the known rapid decline in the first few decades followed by a millennium-scale tail. For a 100 Gt-C emission pulse added to a constant CO2 concentration of 389 ppm, 25 ± 9% is still found in the atmosphere after 1000 yr; the ocean has absorbed 59 ± 12% and the land the remainder (16 ± 14%). The response in global mean surface air temperature is an increase by 0.20 ± 0.12 °C within the first twenty years; thereafter and until year 1000, temperature decreases only slightly, whereas ocean heat content and sea level continue to rise. Our best estimate for the Absolute Global Warming Potential, given by the time-integrated response in CO2 at year 100 multiplied by its radiative efficiency, is 92.5 × 10−15 yr W m−2 per kg-CO2. This value very likely (5 to 95% confidence) lies within the range of (68 to 117) × 10−15 yr W m−2 per kg-CO2. Estimates for time-integrated response in CO2 published in the IPCC First, Second, and Fourth Assessment and our multi-model best estimate all agree within 15% during the first 100 yr. The integrated CO2 response, normalized by the pulse size, is lower for pre-industrial conditions, compared to present day, and lower for smaller pulses than larger pulses. In contrast, the response in temperature, sea level and ocean heat content is less sensitive to these choices. Although, choices in pulse size, background concentration, and model lead to uncertainties, the most important and subjective choice to determine AGWP of CO2 and GWP is the time horizon. |
Databáze: | OpenAIRE |
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