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      Improved calculation of warming-equivalent emissions for short-lived climate pollutants

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          Abstract

          Anthropogenic global warming at a given time is largely determined by the cumulative total emissions (or stock) of long-lived climate pollutants (LLCPs), predominantly carbon dioxide (CO 2), and the emission rates (or flow) of short-lived climate pollutants (SLCPs) immediately prior to that time. Under the United Nations Framework Convention on Climate Change (UNFCCC), reporting of greenhouse gas emissions has been standardised in terms of CO 2-equivalent (CO 2-e) emissions using Global Warming Potentials (GWP) over 100-years, but the conventional usage of GWP does not adequately capture the different behaviours of LLCPs and SLCPs, or their impact on global mean surface temperature. An alternative usage of GWP, denoted GWP*, overcomes this problem by equating an increase in the emission rate of an SLCP with a one-off “pulse” emission of CO 2. We show that this approach, while an improvement on the conventional usage, slightly underestimates the impact of recent increases in SLCP emissions on current rates of warming because the climate does not respond instantaneously to radiative forcing. We resolve this with a modification of the GWP* definition, which incorporates a term for each of the short-timescale and long-timescale climate responses to changes in radiative forcing. The amended version allows “CO 2-warming-equivalent” (CO 2-we) emissions to be calculated directly from reported emissions. Thus SLCPs can be incorporated directly into carbon budgets consistent with long-term temperature goals, because every unit of CO 2-we emitted generates approximately the same amount of warming, whether it is emitted as a SLCP or a LLCP. This is not the case for conventionally derived CO 2-e.

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          Irreversible climate change due to carbon dioxide emissions.

          The severity of damaging human-induced climate change depends not only on the magnitude of the change but also on the potential for irreversibility. This paper shows that the climate change that takes place due to increases in carbon dioxide concentration is largely irreversible for 1,000 years after emissions stop. Following cessation of emissions, removal of atmospheric carbon dioxide decreases radiative forcing, but is largely compensated by slower loss of heat to the ocean, so that atmospheric temperatures do not drop significantly for at least 1,000 years. Among illustrative irreversible impacts that should be expected if atmospheric carbon dioxide concentrations increase from current levels near 385 parts per million by volume (ppmv) to a peak of 450-600 ppmv over the coming century are irreversible dry-season rainfall reductions in several regions comparable to those of the "dust bowl" era and inexorable sea level rise. Thermal expansion of the warming ocean provides a conservative lower limit to irreversible global average sea level rise of at least 0.4-1.0 m if 21st century CO(2) concentrations exceed 600 ppmv and 0.6-1.9 m for peak CO(2) concentrations exceeding approximately 1,000 ppmv. Additional contributions from glaciers and ice sheet contributions to future sea level rise are uncertain but may equal or exceed several meters over the next millennium or longer.
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            Emission budgets and pathways consistent with limiting warming to 1.5 °C

            If CO2 emissions after 2015 do not exceed 200 GtC, climate warming after 2015 will fall below 0.6 °C in 66% of CMIP5 models, according to an analysis based on combining a simple climate–carbon-cycle model with estimated ranges for key climate system properties.
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              Alternatives to the Global Warming Potential for Comparing Climate Impacts of Emissions of Greenhouse Gases

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                Author and article information

                Journal
                101749348
                NPJ Clim Atmos Sci
                NPJ Clim Atmos Sci
                NPJ climate and atmospheric science
                2397-3722
                15 October 2019
                04 September 2019
                25 October 2019
                : 2
                : 29
                Affiliations
                [1 ]Environmental Change Institute, School of Geography and the Environment, University of Oxford, South Parks Road, Oxford OX1 3QY, UK
                [2 ]Oxford Martin School, University of Oxford, 34 Broad Street, Oxford OX1 3BD, UK
                [3 ]Atmospheric Oceanic and Planetary Physics, Department of Physics, University of Oxford, Parks Road, Oxford OX1 3PU, UK
                [4 ]Center for International Climate and Environmental Research (CICERO), PO Box 1129 Blindern, 0318 Oslo, Norway
                [5 ]New Zealand Climate Change Research Institute, Victoria University of Wellington, PO Box 600, Wellington, New Zealand
                [6 ]Institute for Governance and Policy Studies, Victoria University of Wellington, PO Box 600, Wellington, New Zealand
                [7 ]Institut d’Etudes Avancées de Nantes, 5, Allée Jacques Berque, 44000 Nantes, France
                Author notes
                Correspondence: Michelle Cain ( michelle.cain@ 123456oxfordmartin.ox.ac.uk )
                Article
                EMS84644
                10.1038/s41612-019-0086-4
                6814445
                31656858
                4a36b1f4-b2c9-4812-879b-a66102aabf79

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