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Desert dust accounts for a large fraction of shortwave radiation absorbed by aerosols, which adds to the climate warming produced by greenhouse gases. However, it remains uncertain exactly how much shortwave radiation dust absorbs. Here, we leverage in-situ measurements of dust single-scattering albedo to constrain absorption at mid-visible wavelength by North African dust, which accounts for approximately half of the global dust. We find that climate and chemical transport models overestimate North African dust absorption aerosol optical depth (AAOD) by up to a factor of two. This occurs primarily because models overestimate the dust imaginary refractive index, the effect of which is partially masked by an underestimation of large dust particles. Similar factors might contribute to an overestimation of AAOD retrieved by the Aerosol Robotic Network, which is commonly used to evaluate climate and chemical transport models. The overestimation of dust absorption by models could lead to substantial biases in simulated dust impacts on the Earth system, including warm biases in dust radiative effects.

Recent analyses show the importance of methane shortwave absorption, which many climate models lack. In particular, Allen et al. (2023) used idealized climate model simulations to show that methane shortwave absorption mutes up to 30 % of the surface warming and 60 % of the precipitation increase associated with its longwave radiative effects. Here, we explicitly quantify the radiative and climate impacts due to shortwave absorption of the present-day methane perturbation. Our results corroborate the hypothesis that present-day methane shortwave absorption mutes the warming effects of longwave absorption. For example, the global mean cooling in response to the present-day methane shortwave absorption is -0.10±0.07 K, which offsets 28 % (7 %–55 %) of the surface warming associated with present-day methane longwave radiative effects. The precipitation increase associated with the longwave radiative effects of the present-day methane perturbation (0.012±0.006 mm d -1) is also muted by shortwave absorption but not significantly so (-0.008±0.009 mm d -1). The unique responses to methane shortwave absorption are related to its negative top-of-the-atmosphere effective radiative forcing but positive atmospheric heating and in part to methane's distinctive vertical atmospheric solar heating profile. We also find that the present-day methane shortwave radiative effects, relative to its longwave radiative effects, are about 5 times larger than those under idealized carbon dioxide perturbations. Additional analyses show consistent but non-significant differences between the longwave versus shortwave radiative effects for both methane and carbon dioxide, including a stronger (negative) climate feedback when shortwave radiative effects are included (particularly for methane). We conclude by reiterating that methane remains a potent greenhouse gas. [ABSTRACT FROM AUTHOR]

Over the past few decades, the geographical distribution of emissions of substances that alter the atmospheric energy balance has changed due to economic growth and air pollution regulations. Here, we show the resulting changes to aerosol and ozone abundances and their radiative forcing using recently updated emission data for the period 1990-2015, as simulated by seven global atmospheric composition models. The models broadly reproduce large-scale changes in surface aerosol and ozone based on observations (e.g.-1 to-3%yr-1 in aerosols over the USA and Europe). The global mean radiative forcing due to ozone and aerosol changes over the 1990-2015 period increased by +0.17±0.08Wm-2, with approximately one-third due to ozone. This increase is more strongly positive than that reported in IPCC AR5. The main reasons for the increased positive radiative forcing of aerosols over this period are the substantial reduction of global mean SO2 emissions, which is stronger in the new emission inventory compared to that used in the IPCC analysis, and higher black carbon emissions.

As global warming progresses, weather conditions like daily temperature and precipitation are changing due to changes in their means and distributions of day-to-day variability. In this study, we show that changes in variability have a stronger influence on the number of extreme precipitation days than the change in the mean state in many locations. We analyze daily precipitation and maximum temperatures at four levels of global warming and under different emission scenarios for the Northern Hemisphere (NH) summer (June - August). Our analysis is based on initial condition large ensemble simulations from three fully coupled Earth System Models (MPI-ESM1-2-LR, CanESM5, and ACCESS-ESM1-5) contributing to the Climate Model Inter-comparison Project phase 6 (CMIP6). We also use information from the Precipitation Driver Response Model Intercomparison Project (PDRMIP) to discern the influence of different climate drivers (notably aerosols and greenhouse gases). We decompose the total changes in daily NH summer precipitation and daily maximum temperature into mean and variability components (standard deviation and skewness). Our results show that in many locations, variability exerts a stronger influence than mean changes on daily precipitation. Changes in the widths and shapes of precipitation distributions are especially dominating over mean changes in Asia, the Arctic and Sub-Saharan Africa. In contrast, temperature changes are primarily driven by changes in the mean state. For the near future (2020-2040), we find that reductions in aerosol emissions would increase the likelihood of extreme summertime precipitation only over Asia. This study emphasizes the importance of incorporating daily variability changes into climate change impact assessments and advocates that future emulator and impact model development should focus on improving the representation of daily variability. [ABSTRACT FROM AUTHOR]

Considerable interest exists in understanding how climate change affects wildfire activity. Here, we use the Community Earth System Model version 2 to show that future anthropogenic aerosol mitigation yields larger increases in fire activity in the Northern Hemisphere boreal forests, relative to a base simulation that lacks climate policy and has large increases in greenhouse gases. The enhanced fire response is related to a deeper layer of summertime soil drying, consistent with increased downwelling surface shortwave radiation and enhanced surface evapotranspiration. In contrast, soil column drying is muted under increasing greenhouse gases due to plant physiological responses to increased carbon dioxide and by enhanced melting of soil ice at a depth that increases soil liquid water. Although considerable uncertainty remains in the representation of fire processes in models, our results suggest that boreal forest fires may be more sensitive to future aerosol mitigation than to greenhouse gas-driven warming. [ABSTRACT FROM AUTHOR]

Observations show a significant increase in Australian summer monsoon (AUSM) rainfall since the mid-twentieth century. Yet the drivers of this trend, including the role of anthropogenic aerosols, remain uncertain. We addressed this knowledge gap using historical simulations from a suite of Coupled Model Intercomparison Project phase 6 (CMIP6) models, the CESM2 Large Ensemble, and idealized single-forcing simulations from the Precipitation Driver Response Model Intercomparison Project (PDRMIP). Our results suggest that Asian anthropogenic aerosol emissions played a key role in the observed increase in AUSM rainfall from 1930 to 2014, alongside the influence of internal variability. Sulfate aerosol emissions over Asia led to regional surface cooling and strengthening of the climatological Siberian high over eastern China, which altered the meridional temperature and sea level pressure gradients across the Indian Ocean. This caused an intensification and southward shift of the Australian monsoonal westerlies (and the local Hadley cell) and resulted in a precipitation increase over northern Australia. Conversely, the influence of increased greenhouse gas concentrations on AUSM rainfall was minimal due to the compensation between thermodynamically induced wettening and transient eddy-induced drying trends. At a larger scale, aerosol and greenhouse gas forcing played a key role in the climate response over the Indo-Pacific sector and eastern equatorial Pacific, respectively (coined the "tropical Pacific east–west divide"). These findings contribute to an improved understanding of the drivers of the multidecadal trend in AUSM rainfall and highlight the need to reduce uncertainties in future projections under different aerosol emission trajectories, which is particularly important for northern Australia's agriculture. Significance Statement: Australian summer monsoon (AUSM) rainfall plays a vital role in sustaining northern Australia's unique biodiversity and extensive agricultural industry. While observations show a significant increase in AUSM rainfall since the mid-twentieth century, the causes remain uncertain. We find that anthropogenic aerosol emissions from Asia played a key role in driving this multidecadal AUSM rainfall trend by inducing dynamic adjustments over the Indo-Pacific sector. These findings highlight the need to consider different aerosol emission trajectories when assessing future projections of AUSM rainfall. [ABSTRACT FROM AUTHOR]

Changes in anthropogenic aerosol emissions have strongly contributed to global and regional trends in temperature, precipitation, and other climate characteristics and have been one of the dominant drivers of decadal trends in Asian and African precipitation. These and other influences on regional climate from changes in aerosol emissions are expected to continue and potentially strengthen in the coming decades. However, a combination of large uncertainties in emission pathways, radiative forcing, and the dynamical response to forcing makes anthropogenic aerosol a key factor in the spread of near-term climate projections, particularly on regional scales, and therefore an important one to constrain. For example, in terms of future emission pathways, the uncertainty in future global aerosol and precursor gas emissions by 2050 is as large as the total increase in emissions since 1850. In terms of aerosol effective radiative forcing, which remains the largest source of uncertainty in future climate change projections, CMIP6 models span a factor of 5, from - 0.3 to - 1.5 W m -2. Both of these sources of uncertainty are exacerbated on regional scales. The Regional Aerosol Model Intercomparison Project (RAMIP) will deliver experiments designed to quantify the role of regional aerosol emissions changes in near-term projections. This is unlike any prior MIP, where the focus has been on changes in global emissions and/or very idealised aerosol experiments. Perturbing regional emissions makes RAMIP novel from a scientific standpoint and links the intended analyses more directly to mitigation and adaptation policy issues. From a science perspective, there is limited information on how realistic regional aerosol emissions impact local as well as remote climate conditions. Here, RAMIP will enable an evaluation of the full range of potential influences of realistic and regionally varied aerosol emission changes on near-future climate. From the policy perspective, RAMIP addresses the burning question of how local and remote decisions affecting emissions of aerosols influence climate change in any given region. Here, RAMIP will provide the information needed to make direct links between regional climate policies and regional climate change. RAMIP experiments are designed to explore sensitivities to aerosol type and location and provide improved constraints on uncertainties driven by aerosol radiative forcing and the dynamical response to aerosol changes. The core experiments will assess the effects of differences in future global and regional (Africa and the Middle East, East Asia, North America and Europe, and South Asia) aerosol emission trajectories through 2051, while optional experiments will test the nonlinear effects of varying emission locations and aerosol types along this future trajectory. All experiments are based on the shared socioeconomic pathways and are intended to be performed with 6th Climate Model Intercomparison Project (CMIP6) generation models, initialised from the CMIP6 historical experiments, to facilitate comparisons with existing projections. Requested outputs will enable the analysis of the role of aerosol in near-future changes in, for example, temperature and precipitation means and extremes, storms, and air quality. [ABSTRACT FROM AUTHOR]

The climate system responds to changes in the amount of atmospheric greenhouse gases or aerosols through rapid processes, triggered within hours and days, and through slower processes, where the full response may only be seen after centuries. In this paper, we aim to elucidate the mechanisms operating on time scales of hours to years to better understand the response of key climate quantities such as energy fluxes, temperature, and precipitation after a sudden increase in either carbon dioxide (CO2), black carbon (BC), or sulfate (SO4) aerosols. The results are based on idealized simulations from six global climate models. We find that the effect of changing ocean temperatures kicks in after a couple of months. Rapid precipitation reductions start occurring instantly and are established after just a few days. For BC, they constitute most of the equilibrium response. For CO2 and SO4, the magnitude of the precipitation response gradually increases as surface warming/cooling evolves, and for CO2, the sign of the response changes from negative to positive after 2 years. Rapid cloud adjustments are typically established within the first 24 h, and while the magnitude of cloud feedbacks for CO2 and SO4 increases over time, the geographical pattern of the equilibrium cloud change is present already after the first year. While there are model differences, our work underscores the overall similarity of the major time-varying processes and responses simulated by current global models and hence the robustness of key features of simulated responses to historical and future anthropogenic forcing. Significance Statement: How does the climate system respond to a change in the amount of atmospheric greenhouse gases or aerosols? Some processes are rapid, responding within hours and days. Others are slow, and the full response to a forcing of the climate may only be seen after centuries. In this paper, we use six global climate models to investigate the time scales of climate responses to carbon dioxide, black carbon, and sulfate, focusing on key climate quantities, such as temperature, precipitation, and clouds. While there are ample model differences, our work underscores the overall similarity of the major time-varying processes and responses simulated by current global models and hence the robustness of key features of simulated responses to historical and future anthropogenic forcing. [ABSTRACT FROM AUTHOR]

While the Intergovernmental Panel on Climate Change (IPCC) physical science reports usually assess a handful of future scenarios, the Working Group III contribution on climate mitigation to the IPCC's Sixth Assessment Report (AR6 WGIII) assesses hundreds to thousands of future emissions scenarios. A key task in WGIII is to assess the global mean temperature outcomes of these scenarios in a consistent manner, given the challenge that the emissions scenarios from different integrated assessment models (IAMs) come with different sectoral and gas-to-gas coverage and cannot all be assessed consistently by complex Earth system models. In this work, we describe the "climate-assessment" workflow and its methods, including infilling of missing emissions and emissions harmonisation as applied to 1202 mitigation scenarios in AR6 WGIII. We evaluate the global mean temperature projections and effective radiative forcing (ERF) characteristics of climate emulators FaIRv1.6.2 and MAGICCv7.5.3 and use the CICERO simple climate model (CICERO-SCM) for sensitivity analysis. We discuss the implied overshoot severity of the mitigation pathways using overshoot degree years and look at emissions and temperature characteristics of scenarios compatible with one possible interpretation of the Paris Agreement. We find that the lowest class of emissions scenarios that limit global warming to "1.5 ∘ C (with a probability of greater than 50 %) with no or limited overshoot" includes 97 scenarios for MAGICCv7.5.3 and 203 for FaIRv1.6.2. For the MAGICCv7.5.3 results, "limited overshoot" typically implies exceedance of median temperature projections of up to about 0.1 ∘ C for up to a few decades before returning to below 1.5 ∘ C by or before the year 2100. For more than half of the scenarios in this category that comply with three criteria for being "Paris-compatible", including net-zero or net-negative greenhouse gas (GHG) emissions, median temperatures decline by about 0.3–0.4 ∘ C after peaking at 1.5–1.6 ∘ C in 2035–2055. We compare the methods applied in AR6 with the methods used for SR1.5 and discuss their implications. This article also introduces a "climate-assessment" Python package which allows for fully reproducing the IPCC AR6 WGIII temperature assessment. This work provides a community tool for assessing the temperature outcomes of emissions pathways and provides a basis for further work such as extending the workflow to include downscaling of climate characteristics to a regional level and calculating impacts. [ABSTRACT FROM AUTHOR]

Changes in anthropogenic aerosol emissions have strongly contributed to global and regional trends in temperature, precipitation, and other climate characteristics, and have been one of the dominant drivers of decadal trends in Asian and African precipitation. These, and other, influences on regional climate from changes in aerosol emissions are expected to continue, and potentially strengthen, in the coming decades. However, a combination of large uncertainties in emissions pathways, radiative forcing, and the dynamical response to forcing makes anthropogenic aerosol a key factor in the spread in near-term climate projections, particularly on regional scales, and therefore an important one to constrain. For example, in terms of future emissions pathways, the uncertainty in future global aerosol and precursor gas emissions by 2050 is as large as the total increase in emissions since 1850. In terms of aerosol effective radiative forcing, which remains the largest source of uncertainty in future climate change projections, CMIP6 models span a factor of five, from -0.3 to -1.5 W m-2. Both of these sources of uncertainty are exacerbated on regional scales. The Regional Aerosol Model Intercomparison Project (RAMIP) will deliver experiments designed to quantify the role of regional aerosol emissions changes in near-term projections. This is unlike any prior MIP, where the focus has been on changes in global emissions and/or very idealized aerosol experiments. Perturbing regional emissions makes RAMIP novel from a scientific standpoint, and links the intended analyses more directly to mitigation and adaptation policy issues. From a science perspective, there is limited information on how realistic regional aerosol emissions impact local as well as remote climate conditions. Here, RAMIP will enable an evaluation of the full range of potential influences of realistic and regionally varied aerosol emission changes on near-future climate. From the policy perspective, RAMIP addresses the burning question of how local and remote decisions affecting emissions of aerosols influence climate change in any given region. Here, RAMIP will provide the information needed to make direct links between regional climate policies and regional climate change. RAMIP experiments are designed to explore sensitivities to aerosol type and location, and provide improved constraints on uncertainties driven by aerosol radiative forcing and the dynamical response to aerosol changes. The core experiments will assess the effects of differences in future global and regional (East Asia, South Asia, Africa and the Middle East) aerosol emission trajectories through 2051, while optional experiments will test the nonlinear effects of varying emission location and aerosol types along this future trajectory. All experiments are based on the Shared Socioeconomic Pathways, and are intended to be performed with sixth Climate Model Intercomparison Project (CMIP6) generation models, initialised from the CMIP6 historical experiments, to facilitate comparisons with existing projections. Requested outputs will enable analysis of the role of aerosol in near-future changes in, for example, temperature and precipitation means and extremes, storms, and air quality. [ABSTRACT FROM AUTHOR]

This study focuses on implications of differences between recent global emissions inventories for simulated trends in anthropogenic aerosol abundances and radiative forcing (RF) over the 1990-2019 period. We use the ECLIPSE version 6 (ECLv6) and Community Emission Data System year 2021 release (CEDS21) as input to the chemical transport model OsloCTM3 and compare the resulting aerosol evolution to corresponding results derived with the first CEDS release, as well as to observed trends in regional and global aerosol optical depth (AOD). Using CEDS21 and ECLv6 results in 3% and 6% lower global mean AOD compared to CEDS in 2014, primarily driven by differences over China and India, where the area average AOD is up to 30% lower. These differences are considerably larger than the satellite-derived interannual variability in AOD. A negative linear trend (over 2005-2017) in global AOD following changes in anthropogenic emissions is found with all three inventories but is markedly stronger with CEDS21 and ECLv6. Furthermore, we confirm that the model better captures the sign and strength of the observed AOD trend over China with CEDS21 and ECLv6 compared to using CEDS. We estimate a net, global mean aerosol-induced RF in 2014 relative to 1990 of 0.08 W m-2 for CEDS21, and 0.12 W m-2 for ECLv6, compared to 0.03 W m-2 with CEDS. Using CEDS21, we also estimate the RF in 2019 relative to 1990 to be 0.10 W m-2, reflecting the continuing decreasing trend in aerosol loads post 2014. Our results facilitate more rigorous comparison between existing and upcoming studies of climate and health effects of aerosols using different emission inventories. [ABSTRACT FROM AUTHOR]

While the IPCC's physical science report usually assesses a handful of future scenarios, the IPCC Sixth Assessment Working Group III report (AR6 WGIII) on climate mitigation assesses hundreds to thousands of future emissions scenarios. A key task is to assess the global-mean temperature outcomes of these scenarios in a consistent manner, given the challenge that the emission scenarios from different integrated assessment models come with different sectoral and gas-to-gas coverage and cannot all be assessed consistently by complex Earth System Models. In this work, we describe the "climate assessment" workflow and its methods, including infilling of missing emissions and emissions harmonisation as applied to 1,202 mitigation scenarios in AR6 WGIII. We evaluate the global-mean temperature projections and effective radiative forcing characteristics (ERF) of climate emulators FaIRv1.6.2, MAGICCv7.5.3, and CICERO-SCM, discuss overshoot severity of the mitigation pathways using overshoot degree years, and look at an interpretation of compatibility with the Paris Agreement. We find that the lowest class of emission scenarios that limit global warming to "1.5 °C (with a probability of greater than 50 %) with no or limited overshoot" includes 90 scenarios for MAGICCv7.5.3, and 196 for FaIRv1.6.2. For the MAGICCv7.5.3 results, "limited overshoot" typically implies exceedance of median temperature projections of up to about 0.1 °C for up to a few decades, before returning to below 1.5 °C by or before the year 2100. For more than half of the scenarios of this category that comply with three criteria for being "Paris-compatible", including net-zero or net-negative greenhouse gas (GHG) emissions, are projected to see median temperatures decline by about 0.3–0.4 °C after peaking at 1.5–1.6 °C in 2035–2055. We compare the methods applied in AR6 with the methods used for SR1.5 and discuss the implications. This article also introduces a 'climate-assessment' Python package which allows for fully reproducing the IPCC AR6 WGIII temperature assessment. This work can be the start of a community tool for assessing the temperature outcomes related to emissions pathways, and potential further work extending the workflow from emissions to global climate by downscaling climate characteristics to a regional level and calculating impacts. [ABSTRACT FROM AUTHOR]

Understanding the regional surface temperature responses to different anthropogenic climate forcing agents, such as greenhouse gases and aerosols, is crucial for understanding past and future regional climate changes. In modern climate models, the regional temperature responses vary greatly for all major forcing agents, but the causes of this variability are poorly understood. Here, we analyze how changes in atmospheric and oceanic energy fluxes due to perturbations in different anthropogenic climate forcing agents lead to changes in global and regional surface temperatures. We use climate model data on idealized perturbations in four major anthropogenic climate forcing agents (CO 2 , CH 4 , sulfate, and black carbon aerosols) from Precipitation Driver Response Model Intercomparison Project (PDRMIP) climate experiments for six climate models (CanESM2, HadGEM2-ES, NCAR-CESM1-CAM4, NorESM1, MIROC-SPRINTARS, GISS-E2). Particularly, we decompose the regional energy budget contributions to the surface temperature responses due to changes in longwave and shortwave fluxes under clear-sky and cloudy conditions, surface albedo changes, and oceanic and atmospheric energy transport. We also analyze the regional model-to-model temperature response spread due to each of these components. The global surface temperature response stems from changes in longwave emissivity for greenhouse gases (CO 2 and CH 4) and mainly from changes in shortwave clear-sky fluxes for aerosols (sulfate and black carbon). The global surface temperature response normalized by effective radiative forcing is nearly the same for all forcing agents (0.63, 0.54, 0.57, 0.61 K W -1 m 2). While the main physical processes driving global temperature responses vary between forcing agents, for all forcing agents the model-to-model spread in temperature responses is dominated by differences in modeled changes in longwave clear-sky emissivity. Furthermore, in polar regions for all forcing agents the differences in surface albedo change is a key contributor to temperature responses and its spread. For black carbon, the modeled differences in temperature response due to shortwave clear-sky radiation are also important in the Arctic. Regional model-to-model differences due to changes in shortwave and longwave cloud radiative effect strongly modulate each other. For aerosols, clouds play a major role in the model spread of regional surface temperature responses. In regions with strong aerosol forcing, the model-to-model differences arise from shortwave clear-sky responses and are strongly modulated by combined temperature responses to oceanic and atmospheric heat transport in the models. [ABSTRACT FROM AUTHOR]

For the radiative impact of individual climate forcings, most previous studies focused on the global mean values at the top of the atmosphere (TOA), and less attention has been paid to surface processes, especially for black carbon (BC) aerosols. In this study, the surface radiative responses to five different forcing agents were analyzed by using idealized model simulations. Our analyses reveal that for greenhouse gases, solar irradiance, and scattering aerosols, the surface temperature changes are mainly dictated by the changes of surface radiative heating, but for BC, surface energy redistribution between different components plays a more crucial role. Globally, when a unit BC forcing is imposed at TOA, the net shortwave radiation at the surface decreases by -5.87±0.67 W m -2 (W m -2) -1 (averaged over global land without Antarctica), which is partially offset by increased downward longwave radiation (2.32±0.38 W m -2 (W m -2) -1 from the warmer atmosphere, causing a net decrease in the incoming downward surface radiation of -3.56±0.60 W m -2 (W m -2) -1. Despite a reduction in the downward radiation energy, the surface air temperature still increases by 0.25±0.08 K because of less efficient energy dissipation, manifested by reduced surface sensible (-2.88±0.43 W m -2 (W m -2) -1) and latent heat flux (-1.54±0.27 W m -2 (W m -2) -1), as well as a decrease in Bowen ratio (-0.20±0.07 (W m -2) -1). Such reductions of turbulent fluxes can be largely explained by enhanced air stability (0.07±0.02 K (W m -2) -1), measured as the difference of the potential temperature between 925 hPa and surface, and reduced surface wind speed (-0.05±0.01 m s -1 (W m -2) -1). The enhanced stability is due to the faster atmospheric warming relative to the surface, whereas the reduced wind speed can be partially explained by enhanced stability and reduced Equator-to-pole atmospheric temperature gradient. These rapid adjustments under BC forcing occur in the lower atmosphere and propagate downward to influence the surface energy redistribution and thus surface temperature response, which is not observed under greenhouse gases or scattering aerosols. Our study provides new insights into the impact of absorbing aerosols on surface energy balance and surface temperature response. [ABSTRACT FROM AUTHOR]

Understanding the regional surface temperature responses to different anthropogenic climate forcing agents, such as greenhouse gases and aerosols, is crucial for understanding past and future regional climate changes. In modern climate models, the regional temperature responses vary greatly for all major forcing agents, but the causes of this variability are poorly understood. Here, we analyse how changes in atmospheric and oceanic energy fluxes due to perturbations in different anthropogenic climate forcing agents lead to changes in global and regional surface temperatures. We use climate model data on idealized perturbations in four major anthropogenic climate forcing agents (CO2, CH4, and sulfate and black carbon aerosols) from PDRMIP climate experiments for six climate models (CanESM2, HadGEM2-ES, NCAR-CESM1-CAM4, NorESM1, MIROC-SPRINTARS, GISS-E2). Particularly, we decompose the regional energy budget contributions to the surface temperature responses due to changes in longwave and shortwave fluxes under clear-sky and cloudy conditions, surface albedo changes, and oceanic and atmospheric energy transport. We also analyse the regional model-to-model temperature response spread due to each of these components. The global surface temperature response stems from changes in longwave emissivity for greenhouse gases (CO2 and CH4) and mainly from changes in shortwave clear-sky fluxes for aerosols (sulfate and black carbon). The global surface temperature response normalized by effective radiative forcing is nearly the same for all forcing agents (0.63, 0.54, 0.57, 0.61 KW-1m²). While the main physical processes driving global temperature responses vary between forcing agents, for all forcing agents the model-to-model spread in temperature responses is dominated by differences in modelled changes in longwave clear-sky emissivity. Furthermore, in polar regions for all forcing agents the differences in surface albedo change is a key contributor to temperature responses and its spread. For black carbon the modelled differences in temperature response due to shortwave clear-sky radiation are also important in the Arctic. Regional model-to-model differences due to changes in shortwave and longwave cloud radiative effect strongly modulate each other. For aerosols clouds play a major role in the model spread of regional surface temperature responses. In regions with strong aerosol forcing the model-to-model differences arise from shortwave clear-sky responses and are strongly modulated by combined temperature responses to oceanic and atmospheric heat transport in the models. [ABSTRACT FROM AUTHOR]

Lockdowns to avoid the spread of COVID-19 have created an unprecedented reduction in human emissions. While the country-level scale of emissions changes can be estimated in near real time, the more detailed, gridded emissions estimates that are required to run general circulation models (GCMs) of the climate will take longer to collect. In this paper we use recorded and projected country-and-sector activity levels to modify gridded predictions from the MESSAGE-GLOBIOM SSP2-4.5 scenario. We provide updated projections for concentrations of greenhouse gases, emissions fields for aerosols, and precursors and the ozone and optical properties that result from this. The code base to perform similar modifications to other scenarios is also provided. We outline the means by which these results may be used in a model intercomparison project (CovidMIP) to investigate the impact of national lockdown measures on climate, including regional temperature, precipitation, and circulation changes. This includes three strands: an assessment of short-term effects (5-year period) and of longer-term effects (30 years) and an investigation into the separate effects of changes in emissions of greenhouse gases and aerosols. This last strand supports the possible attribution of observed changes in the climate system; hence these simulations will also form part of the Detection and Attribution Model Intercomparison Project (DAMIP). [ABSTRACT FROM AUTHOR]

Lockdowns to avoid the spread of COVID-19 have created an unprecedented reduction in human emissions. While the country-level scale of emissions changes can be estimated in near-real-time, the more detailed, gridded emissions estimates that are required to run General Circulation Models (GCM) of the climate will take longer to collect. In this paper we use recorded and projected country-and-sector activity levels to modify gridded predictions from the MESSAGE-GLOBIOM SSP2-4.5 scenario. We provide updated projections for concentrations of greenhouse gases, emissions fields for aerosols and precursors, and the ozone and optical properties that result from this. The codebase to perform similar modifications to other scenarios is also provided. We outline the means by which these results may be used in a model intercomparison project (CovidMIP) to investigate the impact of national lockdown measures on climate. This includes three strands: an assessment of short-term effects (5-year period), of longer-term effects (30 years) and an investigation into the separate effects of changes in emissions of greenhouse gases and aerosols. This last strand supports possible attribution of observed changes in the climate system, hence these simulations will also form part of the Detection and Attribution Model Intercomparison Project (DAMIP). [ABSTRACT FROM AUTHOR]

The diurnal temperature range (DTR) (or difference between the maximum and minimum temperature within a day) is one of many climate parameters that affects health, agriculture and society. Understanding how DTR evolves under global warming is therefore crucial. Physically different drivers of climate change, such as greenhouse gases and aerosols, have distinct influences on global and regional climate. Therefore, predicting the future evolution of DTR requires knowledge of the effects of individual climate forcers, as well as of the future emissions mix, in particular in high-emission regions. Using global climate model simulations from the Precipitation Driver and Response Model Intercomparison Project (PDRMIP), we investigate how idealized changes in the atmospheric levels of a greenhouse gas (CO2) and aerosols (black carbon and sulfate) influence DTR (globally and in selected regions). We find broad geographical patterns of annual mean change that are similar between climate drivers, pointing to a generalized response to global warming which is not defined by the individual forcing agents. Seasonal and regional differences, however, are substantial, which highlights the potential importance of local background conditions and feedbacks. While differences in DTR responses among drivers are minor in Europe and North America, there are distinctly different DTR responses to aerosols and greenhouse gas perturbations over India and China, where present aerosol emissions are particularly high. BC induces substantial reductions in DTR, which we attribute to strong modeled BC-induced cloud responses in these regions. [ABSTRACT FROM AUTHOR]

There is a large range of future aerosol emissions scenarios explored in the Shared Socioeconomic Pathways (SSPs), with plausible pathways spanning a range of possibilities from large global reductions in emissions by 2050 to moderate global increases over the same period. Diversity in emissions across the pathways is particularly large over Asia. Rapid reductions in anthropogenic aerosol and precursor emissions between the present day and the 2050s lead to enhanced increases in global and Asian summer monsoon precipitation relative to scenarios with weak air quality policies. However, the effects of aerosol reductions do not persist to the end of the 21st century for precipitation, when instead the response to greenhouse gases dominates differences across the SSPs. The relative magnitude and spatial distribution of aerosol changes are particularly important for South Asian summer monsoon precipitation changes. Precipitation increases here are initially suppressed in SSPs 2-4.5, 3-7.0, and 5-8.5 relative to SSP1-1.9 when the impact of remote emission decreases is counteracted by continued increases in South Asian emissions. [ABSTRACT FROM AUTHOR]

Mitigation of non-CO 2 emissions plays a key role in meeting the Paris Agreement ambitions and sustainable development goals. Implementation of respective policies addressing these targets mainly occur at sectoral and regional levels, and designing efficient mitigation strategies therefore relies on detailed knowledge about the mix of emissions from individual sources and their subsequent climate impact. Here we present a comprehensive dataset of near- and long-term global temperature responses to emissions of CO 2 and individual short-lived climate forcers (SLCFs) from 7 sectors and 13 regions – for both present-day emissions and their continued evolution as projected under the Shared Socioeconomic Pathways (SSPs). We demonstrate the key role of CO 2 in driving both near- and long-term warming and highlight the importance of mitigating methane emissions from agriculture, waste management, and energy production as the primary strategy to further limit near-term warming. Due to high current emissions of cooling SLCFs, policies targeting end-of-pipe energy sector emissions may result in net added warming unless accompanied by simultaneous methane and/or CO 2 reductions. We find that SLCFs are projected to play a continued role in many regions, particularly those including low- to medium-income countries, under most of the SSPs considered here. East Asia, North America, and Europe will remain the largest contributors to total net warming until 2100, regardless of scenario, while South Asia and Africa south of the Sahara overtake Europe by the end of the century in SSP3-7.0 and SSP5-8.5. Our dataset is made available in an accessible format, aimed also at decision makers, to support further assessment of the implications of policy implementation at the sectoral and regional scales. [ABSTRACT FROM AUTHOR]

Shortwave cloud radiative effects (SWCREs), defined as the difference of the shortwave radiative flux between all-sky and clear-sky conditions at the surface, have been reported to play an important role in influencing the Earth's energy budget and temperature extremes. In this study, we employed a set of global climate models to examine the SWCRE responses to CO2, black carbon (BC) aerosols, and sulfate aerosols in boreal summer over the Northern Hemisphere. We found that CO2 causes positive SWCRE changes over most of the NH, and BC causes similar positive responses over North America, Europe, and eastern China but negative SWCRE over India and tropical Africa. When normalized by effective radiative forcing, the SWCRE from BC is roughly 3-5 times larger than that from CO2. SWCRE change is mainly due to cloud cover changes resulting from changes in relative humidity (RH) and, to a lesser extent, changes in cloud liquid water, circulation, dynamics, and stability. The SWCRE response to sulfate aerosols, however, is negligible compared to that for CO2 and BC because part of the radiation scattered by clouds under all-sky conditions will also be scattered by aerosols under clear-sky conditions. Using a multilinear regression model, it is found that mean daily maximum temperature (Tmax) increases by 0.15 and 0.13K per watt per square meter (Wm􀀀2) increase in local SWCRE under the CO2 and BC experiment, respectively. When domain-averaged, the contribution of SWCRE change to summer mean Tmax changes was 10%-30% under CO2 forcing and 30%-50% under BC forcing, varying by region, which can have important implications for extreme climatic events and socioeconomic activities. [ABSTRACT FROM AUTHOR]

The radiative forcing of the aerosol–radiation interaction can be decomposed into clear-sky and cloudy-sky portions. Two sets of multi-model simulations within Aerosol Comparisons between Observations and Models (AeroCom), combined with observational methods, and the time evolution of aerosol emissions over the industrial era show that the contribution from cloudy-sky regions is likely weak. A mean of the simulations considered is 0.01±0.1 W m -2. Multivariate data analysis of results from AeroCom Phase II shows that many factors influence the strength of the cloudy-sky contribution to the forcing of the aerosol–radiation interaction. Overall, single-scattering albedo of anthropogenic aerosols and the interaction of aerosols with the short-wave cloud radiative effects are found to be important factors. A more dedicated focus on the contribution from the cloud-free and cloud-covered sky fraction, respectively, to the aerosol–radiation interaction will benefit the quantification of the radiative forcing and its uncertainty range. [ABSTRACT FROM AUTHOR]

Shortwave cloud radiative effects (SWCRE), defined as the difference of shortwave radiative flux between all-sky and clear-sky conditions, have been reported to play an important role in influencing the Earth's energy budget and temperature extremes. In this study, we employed a set of global climate models to examine the SWCRE responses to CO2, black carbon (BC) aerosols and sulfate aerosols in boreal summer over the Northern Hemisphere. We found that CO2 causes positive SWCRE changes over most of the NH, and BC causes similar positive responses over North America, Europe and East China but negative SWCRE over India and tropical Africa. When normalized by effective radiative forcing, the SWCRE from BC is roughly 3-5 times larger than that from CO2. SWCRE change is mainly due to cloud cover changes resulting from the changes in relative humidity (RH) and, to a lesser extent, changes in circulation and stability. The SWCRE response to sulfate aerosols, however, is negligible compared to that for CO2 and BC. Using a multilinear regression model, it is found that mean daily maximum temperature (Tmax) increases by 0.15 K and 0.13 K per W m-2 increase in local SWCRE under the CO2 and BC experiment, respectively. When domain-averaged, the SWCRE change contribution to summer mean Tmax changes was 10-30 % under CO2 forcing and 30-50 % under BC forcing, varying by region, which can have important implications for extreme climatic events and socio-economic activities. [ABSTRACT FROM AUTHOR]

Here we present results from the first phase of the Reduced Complexity Model Intercomparison Project (RCMIP). RCMIP is a systematic examination of reduced complexity climate models (RCMs), which are used to complement and extend the insights from more complex Earth System Models (ESMs), in particular those participating in the Sixth Coupled Model Intercomparison Project (CMIP6). In Phase 1 of RCMIP, with 14 participating models namely ACC2, AR5IR (2 and 3 box versions), CICERO-SCM, ESCIMO, FaIR, GIR, GREB, Hector, Held et al. two layer model, MAGICC, MCE, OSCAR and WASP, we highlight the structural differences across various RCMs and show that RCMs are capable of reproducing global-mean surface air temperature (GSAT) changes of ESMs and historical observations. We find that some RCMs are capable of emulating the GSAT response of CMIP6 models to within a root-mean square error of 0.2°C (of the same order of magnitude as ESM internal variability) over a range of scenarios. Running the same model configurations for both RCP and SSP scenarios, we see that the SSPs exhibit higher effective radiative forcing throughout the second half of the 21st Century. Comparing our results to the difference between CMIP5 and CMIP6 output, we find that the change in scenario explains approximately 46% of the increase in higher end projected warming between CMIP5 and CMIP6. This suggests that changes in ESMs from CMIP5 to CMIP6 explain the rest of the increase, hence the higher climate sensitivities of available CMIP6 models may not be having as large an impact on GSAT projections as first anticipated. A second phase of RCMIP will complement RCMIP Phase 1 by exploring probabilistic results and emulation in more depth to provide results available for the IPCC's Sixth Assessment Report author teams. [ABSTRACT FROM AUTHOR]

The radiative forcing of the aerosol-radiation interaction can be decomposed into clear sky and cloudy sky portions. Two sets of multi-model simulations within AeroCom, combined with observational methods, and the time evolution of aerosol emissions over the industrial era show that the contribution from cloudy sky regions is likely weak. A mean of the simulations considered is 0.01 ± 0.1 W m−2. Multivariate data analysis of results from AeroCom Phase II shows that many factors influence the strength of the cloudy sky contribution to the forcing of the aerosol-radiation interaction. Overall, single scattering albedo of anthropogenic aerosols and the interaction of aerosols with the shortwave cloud radiative effects are found to be important factors. A more dedicated focus on the contribution from the cloud free and cloud covered sky fraction respectively to the aerosol-radiation interaction will benefit the quantification of the radiative forcing and its uncertainty range. [ABSTRACT FROM AUTHOR]

Emissions of anthropogenic aerosols are expected to change drastically over the coming decades, with potentially significant climate implications. Using the most recent generation of harmonized emission scenarios, the Shared Socioeconomic Pathways (SSPs) as input to a global chemistry transport and radiative transfer model, we provide estimates of the projected future global and regional burdens and radiative forcing of anthropogenic aerosols under three contrasting pathways for air pollution levels: SSP1-1.9, SSP2-4.5 and SSP3-7.0. We find that the broader range of future air pollution emission trajectories spanned by the SSPs compared to previous scenarios translates into total aerosol forcing estimates in 2100 relative to 1750 ranging from -0.04 in SSP1-1.9 to -0.51 W m -2 in SSP3-7.0. Compared to our 1750–2015 estimate of -0.55 W m -2 , this shows that, depending on the success of air pollution policies and socioeconomic development over the coming decades, aerosol radiative forcing may weaken by nearly 95 % or remain close to the preindustrial to present-day level. In all three scenarios there is a positive forcing in 2100 relative to 2015, from 0.51 in SSP1-1.9 to 0.04 W m -2 in SSP3-7.0. Results also demonstrate significant differences across regions and scenarios, especially in South Asia and Africa. While rapid weakening of the negative aerosol forcing following effective air quality policies will unmask more of the greenhouse-gas-induced global warming, slow progress on mitigating air pollution will significantly enhance the atmospheric aerosol levels and risk to human health in these regions. In either case, the resulting impacts on regional and global climate can be significant. [ABSTRACT FROM AUTHOR]

Water vapour in the atmosphere is the source of a major climate feedback mechanism and potential increases in the availability of water vapour could have important consequences for mean and extreme precipitation. Future precipitation changes further depend on how the hydrological cycle responds to different drivers of climate change, such as greenhouse gases and aerosols. Currently, neither the total anthropogenic influence on the hydrological cycle nor that from individual drivers is constrained sufficiently to make solid projections. We investigate how integrated water vapour (IWV) responds to different drivers of climate change. Results from 11 global climate models have been used, based on simulations where CO2 , methane, solar irradiance, black carbon (BC), and sulfate have been perturbed separately. While the global-mean IWV is usually assumed to increase by ∼7 % per kelvin of surface temperature change, we find that the feedback response of IWV differs somewhat between drivers. Fast responses, which include the initial radiative effect and rapid adjustments to an external forcing, amplify these differences. The resulting net changes in IWV range from 6.4±0.9 % K -1 for sulfate to 9.8±2 % K -1 for BC. We further calculate the relationship between global changes in IWV and precipitation, which can be characterized by quantifying changes in atmospheric water vapour lifetime. Global climate models simulate a substantial increase in the lifetime, from 8.2±0.5 to 9.9±0.7 d between 1986–2005 and 2081–2100 under a high-emission scenario, and we discuss to what extent the water vapour lifetime provides additional information compared to analysis of IWV and precipitation separately. We conclude that water vapour lifetime changes are an important indicator of changes in precipitation patterns and that BC is particularly efficient in prolonging the mean time, and therefore likely the distance, between evaporation and precipitation. [ABSTRACT FROM AUTHOR]

Anthropogenic emissions of short-lived climate forcers (SLCFs) affect both air quality and climate. How much regional temperatures are affected by ambitious SLCF emission mitigation policies, is however still uncertain. We investigate the potential temperature implications of stringent air quality policies, by applying matrices of regional temperature responses to new pathways for future anthropogenic emissions of aerosols, methane (CH4) and other short-lived gases. These measures have only minor impact on CO2 emissions. Two main options are explored, one with climate optimal reductions (i.e. constructed to yield a maximum global cooling) and one with maximum technically feasible reductions. The temperature response is calculated for four latitude response bands (90-28° S, 28° S-28° N, 28-60° N, and 60-90° N) by using existing regional temperature change potential (ARTP) values for four emission regions: Europe, East Asia, shipping, and the rest of the world. By 2050, we find that global surface temperature can be reduced by -0.3 ± 0.08 °C with climate-optimal mitigation of SLCFs relative to a baseline scenario, and as much as -0.7 °C in the Arctic. Cutting CH4 and BC emissions contribute the most. This could offset warming equal to approximately 15 years of current global CO2 emissions. If SLCFs are mitigated heavily, we find a net warming of about 0.1 °C, but when uncertainties are included a slight cooling is also possible. In the climate optimal scenario, the largest contributions to cooling comes from the energy, domestic, waste, and transportation sectors. In the maximum technically feasible mitigation scenario, emission changes from the sectors industry, energy, and shipping will give warming. Some measures, such as in the sectors agriculture waste burning, domestic, transport, and industry, have outsized impact on the Arctic, especially by cutting BC emissions in winter in areas near the Arctic. [ABSTRACT FROM AUTHOR]

The relationship between changes in integrated water vapour (IWV) and precipitation can be characterized by quantifying changes in atmospheric water vapour lifetime. Precipitation isotope ratios correlate with this lifetime, a relationship that helps understand dynamical processes and may lead to improved climate projections. We investigate how water vapour and its lifetime respond to different drivers of climate change, such as greenhouse gases and aerosols. Results from 11 global climate models have been used, based on simulations where CO2, methane, solar irradiance, black carbon (BC), and sulphate have been perturbed separately. A lifetime increase from 8 to 10 days is projected between 1986–2005 and 2081–2100, under a business-as-usual pathway. By disentangling contributions from individual climate drivers, we present a physical understanding of how global warming slows down the hydrological cycle, due to longer lifetime, but still amplifies the cycle due to stronger precipitation/evaporation fluxes. The feedback response of IWV to surface temperature change differs somewhat between drivers. Fast responses amplify these differences and lead to net changes in IWV per degree surface warming ranging from 6.4±0.9 %/K for sulphate to 9.8±2 %/K for BC. While BC is the driver with the strongest increase in IWV per degree surface warming, it is also the only driver with a reduction in precipitation per degree surface warming. Consequently, increases in BC aerosol concentrations yield the strongest slowdown of the hydrological cycle among the climate drivers studied, with a change in water vapour lifetime per degree surface warming of 1.1±0.4 days/K, compared to less than 0.5 days/K for the other climate drivers (CO2, methane, solar irradiance, sulphate). [ABSTRACT FROM AUTHOR]

Atmospheric aerosols and greenhouse gases affect cloud properties, radiative balance and, thus, the hydrological cycle. Observations show that precipitation has decreased in the Mediterranean since the beginning of the 20th century, and many studies have investigated possible mechanisms. So far, however, the effects of aerosol forcing on Mediterranean precipitation remain largely unknown. Here we compare the modeled dynamical response of Mediterranean precipitation to individual forcing agents in a set of global climate models (GCMs). Our analyses show that both greenhouse gases and aerosols can cause drying in the Mediterranean and that precipitation is more sensitive to black carbon (BC) forcing than to well-mixed greenhouse gases (WMGHGs) or sulfate aerosol. In addition to local heating, BC appears to reduce precipitation by causing an enhanced positive sea level pressure (SLP) pattern similar to the North Atlantic Oscillation–Arctic Oscillation, characterized by higher SLP at midlatitudes and lower SLP at high latitudes. WMGHGs cause a similar SLP change, and both are associated with a northward diversion of the jet stream and storm tracks, reducing precipitation in the Mediterranean while increasing precipitation in northern Europe. Though the applied forcings were much larger, if forcings are scaled to those of the historical period of 1901–2010, roughly one-third (31±17 %) of the precipitation decrease would be attributable to global BC forcing with the remainder largely attributable to WMGHGs, whereas global scattering sulfate aerosols would have negligible impacts. Aerosol–cloud interactions appear to have minimal impacts on Mediterranean precipitation in these models, at least in part because many simulations did not fully include such processes; these merit further study. The findings from this study suggest that future BC and WMGHG emissions may significantly affect regional water resources, agricultural practices, ecosystems and the economy in the Mediterranean region. [ABSTRACT FROM AUTHOR]

Atmospheric aerosols and greenhouse gases affect cloud properties, radiative balance and thus, the hydrological cycle. Observations show that precipitation has decreased in the Mediterranean since the 20th century, and many studies have investigated possible mechanisms. So far, however, the effects of aerosol forcing on Mediterranean precipitation remain largely unknown. Here we compare Mediterranean precipitation responses to individual forcing agents in a set of state-of-the-art global climate models (GCMs). Our analyses show that both greenhouse gases and aerosols can cause drying in the Mediterranean, and that precipitation is more sensitive to black carbon (BC) forcing than to well-mixed greenhouse gases (WMGHGs) or sulfate aerosol. In addition to local heating, BC appears to reduce precipitation by causing an enhanced positive North Atlantic Oscillation (NAO)/Arctic Oscillation (AO)-like sea level pressure (SLP) pattern, characterized by higher SLP at mid-latitudes and lower SLP at high-latitudes. WMGHGs cause a similar SLP change, and both are associated with a northward diversion of the jet stream and storm tracks, reducing precipitation in the Mediterranean while increasing precipitation in Northern Europe. Though the applied forcings were much larger, if forcings are scaled to those of the historical period of 1901–2010, roughly one-third (31 ± 17 %) of the precipitation decrease would be attributable to global BC forcing with the remainder largely attributable to WMGHGs whereas global scattering sulfate aerosols have negligible impacts. The results from this study suggest that future BC emissions may significantly affect regional water resources, agricultural practices, ecosystems, and the economy in the Mediterranean region. [ABSTRACT FROM AUTHOR]

Atmospheric aerosols from anthropogenic and natural sources reach the polar regions through long-range transport and affect the local radiation balance. Such transport is, however, poorly constrained in present-day global climate models, and few multi-model evaluations of polar anthropogenic aerosol radiative forcing exist. Here we compare the aerosol optical depth (AOD) at 550 nm from simulations with 16 global aerosol models from the AeroCom Phase II model intercomparison project with available observations at both poles. We show that the annual mean multi-model median is representative of the observations in Arctic, but that the intermodel spread is large. We also document the geographical distribution and seasonal cycle of the AOD for the individual aerosol species: black carbon (BC) from fossil fuel and biomass burning, sulfate, organic aerosols (OAs), dust, and sea-salt. For a subset of models that represent nitrate and secondary organic aerosols (SOAs), we document the role of these aerosols at high latitudes. The seasonal dependence of natural and anthropogenic aerosols differs with natural aerosols peaking in winter (seasalt) and spring (dust), whereas AOD from anthropogenic aerosols peaks in late spring and summer. The models produce a median annual mean AOD of 0.07 in the Arctic (defined here as north of 60° N). The models also predict a noteworthy aerosol transport to the Antarctic (south of 70° S) with a resulting AOD varying between 0.01 and 0.02. The models have estimated the shortwave anthropogenic radiative forcing contributions to the direct aerosol effect (DAE) associated with BC and OA from fossil fuel and biofuel (FF), sulfate, SOAs, nitrate, and biomass burning from BC and OA emissions combined. The Arctic modelled annual mean DAE is slightly negative (-0.12 W m-2), dominated by a positive BC FF DAE in spring and a negative sulfate DAE in summer. The Antarctic DAE is governed by BC FF. We perform sensitivity experiments with one of the AeroCom models (GISS modelE) to investigate how regional emissions of BC and sulfate and the lifetime of BC influence the Arctic and Antarctic AOD. A doubling of emissions in eastern Asia results in a 33% increase in Arctic AOD of BC. A doubling of the BC lifetime results in a 39% increase in Arctic AOD of BC. However, these radical changes still fall within the AeroCom model range. [ABSTRACT FROM AUTHOR]