scholarly journals Anthropogenic aerosol forcing under the Shared Socioeconomic Pathways

2019 ◽  
Author(s):  
Marianne T. Lund ◽  
Gunnar Myhre ◽  
Bjørn H. Samset

Abstract. 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 different levels of air pollution control: strong (SSP1), medium (SSP2) and weak (SSP3). 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 W m−2 in SSP1-1.9 to −0.51 W m−2 in SSP3-7.0. Compared to our 1750–2015 estimate of −0.61 W m−2, this shows that depending on the success of air pollution policies over the coming decades, aerosol radiative forcing may weaken by nearly 95 % or remain close to the pre-industrial to present-day level. In all three scenarios there is a positive forcing in 2100 relative to 2015, from 0.51 W m−2 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 either case, the resulting impacts on regional and global climate can be significant.

2019 ◽  
Vol 19 (22) ◽  
pp. 13827-13839 ◽  
Author(s):  
Marianne T. Lund ◽  
Gunnar Myhre ◽  
Bjørn H. Samset

Abstract. 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.


2008 ◽  
Vol 8 (21) ◽  
pp. 6405-6437 ◽  
Author(s):  
S. Kloster ◽  
F. Dentener ◽  
J. Feichter ◽  
F. Raes ◽  
J. van Aardenne ◽  
...  

Abstract. We apply different aerosol and aerosol precursor emission scenarios reflecting possible future control strategies for air pollution in the ECHAM5-HAM model, and simulate the resulting effect on the Earth's radiation budget. We use two opposing future mitigation strategies for the year 2030: one in which emission reduction legislation decided in countries throughout the world are effectively implemented (current legislation; CLE 2030) and one in which all technical options for emission reductions are being implemented independent of their cost (maximum feasible reduction; MFR 2030). We consider the direct, semi-direct and indirect radiative effects of aerosols. The total anthropogenic aerosol radiative forcing defined as the difference in the top-of-the-atmosphere radiation between 2000 and pre-industrial times amounts to −2.00 W/m2. In the future this negative global annual mean aerosol radiative forcing will only slightly change (+0.02 W/m2) under the "current legislation" scenario. Regionally, the effects are much larger: e.g. over Eastern Europe radiative forcing would increase by +1.50 W/m2 because of successful aerosol reduction policies, whereas over South Asia it would decrease by −1.10 W/m2 because of further growth of emissions. A "maximum feasible reduction" of aerosols and their precursors would lead to an increase of the global annual mean aerosol radiative forcing by +1.13 W/m2. Hence, in the latter case, the present day negative anthropogenic aerosol forcing could be more than halved by 2030 because of aerosol reduction policies and climate change thereafter will be to a larger extent be controlled by greenhouse gas emissions. We combined these two opposing future mitigation strategies for a number of experiments focusing on different sectors and regions. In addition, we performed sensitivity studies to estimate the importance of future changes in oxidant concentrations and the importance of the aerosol microphysical coupling within the range of expected future changes. For changes in oxidant concentrations caused by future air pollution mitigation, we do not find a significant effect for the global annual mean radiative aerosol forcing. In the extreme case of only abating SO2 or carbonaceous emissions to a maximum feasible extent, we find deviations from additivity for the radiative forcing over anthropogenic source regions up to 10% compared to an experiment abating both at the same time.


2014 ◽  
Vol 14 (11) ◽  
pp. 5513-5527 ◽  
Author(s):  
C. L. Heald ◽  
D. A. Ridley ◽  
J. H. Kroll ◽  
S. R. H. Barrett ◽  
K. E. Cady-Pereira ◽  
...  

Abstract. The direct radiative effect (DRE) of aerosols, which is the instantaneous radiative impact of all atmospheric particles on the Earth's energy balance, is sometimes confused with the direct radiative forcing (DRF), which is the change in DRE from pre-industrial to present-day (not including climate feedbacks). In this study we couple a global chemical transport model (GEOS-Chem) with a radiative transfer model (RRTMG) to contrast these concepts. We estimate a global mean all-sky aerosol DRF of −0.36 Wm−2 and a DRE of −1.83 Wm−2 for 2010. Therefore, natural sources of aerosol (here including fire) affect the global energy balance over four times more than do present-day anthropogenic aerosols. If global anthropogenic emissions of aerosols and their precursors continue to decline as projected in recent scenarios due to effective pollution emission controls, the DRF will shrink (−0.22 Wm−2 for 2100). Secondary metrics, like DRE, that quantify temporal changes in both natural and anthropogenic aerosol burdens are therefore needed to quantify the total effect of aerosols on climate.


2017 ◽  
Vol 30 (16) ◽  
pp. 6585-6589 ◽  
Author(s):  
Bjorn Stevens ◽  
Stephanie Fiedler

Kretzschmar et al., in a comment in 2017, use the spread in the output of aerosol–climate models to argue that the models refute the hypothesis (presented in a paper by Stevens in 2015) that for the mid-twentieth-century warming to be consistent with observations, then the present-day aerosol forcing, [Formula: see text] must be less negative than −1 W m−2. The main point of contention is the nature of the relationship between global SO2 emissions and [Formula: see text] In contrast to the concave (log-linear) relationship used by Stevens and in earlier studies, whereby [Formula: see text] becomes progressively less sensitive to SO2 emissions, some models suggest a convex relationship, which would imply a less negative lower bound. The model that best exemplifies this difference, and that is most clearly in conflict with the hypothesis of Stevens, does so because of an implausible aerosol response to the initial rise in anthropogenic aerosol precursor emissions in East and South Asia—already in 1975 this model’s clear-sky reflectance from anthropogenic aerosol over the North Pacific exceeds present-day estimates of the clear-sky reflectance by the total aerosol. The authors perform experiments using a new (observationally constrained) climatology of anthropogenic aerosols to further show that the effects of changing patterns of aerosol and aerosol precursor emissions during the late twentieth century have, for the same global emissions, relatively little effect on [Formula: see text] These findings suggest that the behavior Kretzschmar et al. identify as being in conflict with the lower bound in Stevens arises from an implausible relationship between SO2 emissions and [Formula: see text] and thus provides little basis for revising this lower bound.


2012 ◽  
Vol 12 (1) ◽  
pp. 193-240 ◽  
Author(s):  
X. Ma ◽  
F. Yu ◽  
G. Luo

Abstract. Aerosol direct radiative forcing (DRF) plays an important role in global climate change but has a large uncertainty. Here we investigate aerosol DRF with GEOS-Chem-APM, a recently developed global aerosol microphysical model that is designed to capture key particle properties (size, composition, coating of primary particles by volatile species, etc.). The model, with comprehensive chemistry, microphysics and up-to-date emission inventories, is driven by assimilated meteorology, which is presumably more realistic compared to the model-predicted meteorology. For this study, the model is extended by incorporating a radiation transfer model. Optical properties are calculated using Mie theory, where the core-shell configuration could be treated with the refractive indices from the recently updated values available in the literature. The surface albedo is taken from MODIS satellite retrievals for the simulation year, in which the data set for the 8-day mean at 1 km resolution for 7 wavebands is provided. We derive the total and anthropogenic aerosol DRF, mainly focus on the results of anthropogenic aerosols, and then compare with those values reported in previous studies. In addition, we examine the anthropogenic aerosol DRF's dependence on several key factors, including the particle size of black carbon (BC) and primary organic carbon (POC), the density of BC and the mixing state. Our studies show that the anthropogenic aerosol DRF at top of atmosphere (TOA) for all sky is −0.41 W m−2. However, the sensitivity experiments suggest that the magnitude could vary from −0.08 W m−2 to −0.61 W m−2 depending on assumptions regarding the mixing state, size and density of particles.


2008 ◽  
Vol 8 (2) ◽  
pp. 5563-5627 ◽  
Author(s):  
S. Kloster ◽  
F. Dentener ◽  
J. Feichter ◽  
F. Raes ◽  
J. van Aardenne ◽  
...  

Abstract. We apply different aerosol and aerosol precursor emission scenarios reflecting possible future control strategies for air pollution in the ECHAM5-HAM model, and simulate the resulting effect on the Earth's radiation budget. We use two opposing future mitigation strategies for the year 2030: one in which emission reduction legislation decided in countries throughout the world are effectively implemented (current legislation; CLE 2030) and one in which all technical options for emission reductions are being implemented independent of their cost (maximum feasible reduction; MFR 2030). We consider the direct, semi-direct and indirect radiative effects of aerosols. The total anthropogenic aerosol radiative forcing defined as the difference in the top-of-the-atmosphere radiation between 2000 and pre-industrial times amounts to −2.05 W/m2. In the future this negative global annual mean aerosol radiative forcing will only slightly change (+0.02 W/m2) under the "current legislation" scenario. Regionally, the effects are much larger: e.g. over Eastern Europe radiative forcing would increase by +1.50 W/m2 because of successful aerosol reduction policies, whereas over South Asia it would decrease by −1.10 W/m2 because of further growth of emissions. A "maximum feasible reduction" of aerosols and their precursors would lead to an increase of the global annual mean aerosol radiative forcing by +1.13 W/m2. Hence, in the latter case, the present day negative anthropogenic aerosol forcing cloud be more than halved by 2030 because of aerosol reduction policies and climate change thereafter will be to a larger extend be controlled by greenhouse gas emissions. We combined these two opposing future mitigation strategies for a number of experiments focusing on different sectors and regions. In addition, we performed sensitivity studies to estimate the importance of future changes in oxidant concentrations and the importance of the aerosol microphysical coupling within the range of expected future changes. For changes in oxidant concentrations in the future within a realistic range, we do not find a significant effect for the global annual mean radiative aerosol forcing. In the extreme case of only abating SO2 or carbonaceous emissions to a maximum feasible extent, we find deviations from additivity for the radiative forcing over anthropogenic source regions up to 10% compared to an experiment abating both at the same time.


2012 ◽  
Vol 12 (12) ◽  
pp. 5563-5581 ◽  
Author(s):  
X. Ma ◽  
F. Yu ◽  
G. Luo

Abstract. Aerosol direct radiative forcing (DRF) plays an important role in global climate change but has a large uncertainty. Here we investigate aerosol DRF with GEOS-Chem-APM, a recently developed global aerosol microphysical model that is designed to capture key particle properties (size, composition, coating of primary particles by volatile species, etc.). The model, with comprehensive chemistry, microphysics and up-to-date emission inventories, is driven by assimilated meteorology, which is presumably more realistic compared to the model-predicted meteorology. For this study, the model is extended by incorporating a radiation transfer model. Optical properties are calculated using Mie theory, where the core-shell configuration could be treated with the refractive indices from the recently updated values available in the literature. The surface albedo is taken from MODIS satellite retrievals for the simulation year, in which the data set for the 8-day mean at 0.05° (5600 m) resolution for 7 wavebands is provided. We derive the total and anthropogenic aerosol DRF, mainly focus on the results of anthropogenic aerosols, and then compare with those values reported in previous studies. In addition, we examine the anthropogenic aerosol DRF's dependence on several key factors, including the particle size of black carbon (BC) and primary organic carbon (POC), the density of BC and the mixing state. Our studies show that the anthropogenic aerosol DRF at top of atmosphere (TOA) for all sky is −0.41 W m−2. However, the sensitivity experiments suggest that the magnitude could vary from −0.08 W m−2 to −0.61 W m−2, depending on assumptions regarding the mixing state, size and density of particles.


2013 ◽  
Vol 13 (12) ◽  
pp. 32925-32961 ◽  
Author(s):  
C. L. Heald ◽  
D. A. Ridley ◽  
J. H. Kroll ◽  
S. R. H. Barrett ◽  
K. E. Cady-Pereira ◽  
...  

Abstract. The direct radiative effect (DRE) of aerosols, which is the instantaneous radiative impact of all atmospheric particles on the Earth's energy balance, is often confused with the direct radiative forcing (DRF), which is the change in DRE from pre-industrial to present-day (not including climate feedbacks). We use here a coupled global chemical transport model (GEOS-Chem) and radiative transfer model (RRTMG) to contrast these concepts. We estimate a global mean all-sky aerosol DRF of −0.36 Wm−2 and a DRE of −1.83 Wm−2 for 2010. Therefore, natural sources of aerosol (here including fire) affect the global energy balance over four times more than do present-day anthropogenic aerosols. If global anthropogenic emissions of aerosols and their precursors continue to decline as projected in recent scenarios due to effective pollution emission controls, the DRF will shrink (−0.22 Wm−2 for 2100), while the climate feedbacks on aerosols under rising global temperatures will likely amplify. Secondary metrics, like DRE, that quantify temporal changes in both natural and anthropogenic aerosol burdens are therefore needed to quantify the total effect of aerosols on climate.


2011 ◽  
Vol 11 (9) ◽  
pp. 25991-26007 ◽  
Author(s):  
R. Makkonen ◽  
A. Asmi ◽  
V.-M. Kerminen ◽  
M. Boy ◽  
A. Arneth ◽  
...  

Abstract. The number of cloud droplets determines several climatically relevant cloud properties. A major cause for the high uncertainty in the indirect aerosol forcing is the availability of cloud condensation nuclei (CCN), which in turn is highly sensitive to atmospheric new particle formation. Here we present the effect of new particle formation on anthropogenic aerosol forcing in present-day (year 2000) and future (year 2100) conditions. The total aerosol forcing (−1.61 W m−2 in year 2000) is simulated to be greatly reduced in the future, to −0.23 W m−2, mainly due to decrease in SO2 emissions and resulting decrease in new particle formation. With the total aerosol forcing decreasing in response to air pollution control measures taking effect, warming from increased greenhouse gas concentrations can potentially increase at a very rapid rate.


2019 ◽  
Author(s):  
Stefan Kinne

Abstract. onthly global maps for aerosol properties of the MACv2 climatology are applied in an off-line radiative transfer model to determine aerosol radiative effects. For details beyond global averages in most cases global maps are presented to visualize regional and seasonal details. Aside from the direct radiative (aerosol presence) effect, including those for aerosol components as extracted from MACv2 aerosol optics, also the major aerosol indirect radiative effect is covered. Hereby, the impact of smaller drops in water clouds due to added anthropogenic aerosol was simulated by applying a satellite retrieval based fit from locally associations between aerosol and drop concentrations over oceans. Present-day anthropogenic aerosols of MACv2 – on a global average basis – reduce the radiative net-fluxes at the top of the atmosphere (TOA) by −1.0 W/m2 and at the surface by −2.1 W/m2. Direct cooling contributions are only about half of indirect contributions (−.35 vs −.65) at TOA, but about twice at the surface (−1.45 vs −.65), as solar absorption of the direct effect warms the atmosphere by +1.1 W/m2. Natural aerosols are on average less absorbing (for a relatively larger solar TOA cooling) and larger in size (now contributing with IR greenhouse warming). Thus, average TOA direct forcing efficiencies for total and anthropogenic aerosol happen to be similar: −11 W/m2/AOD at all-sky and −24 W/m2/AOD at clear-sky conditions. The present-day direct impact by all soot (BC) is globally averaged +0.55W/m2 and at least half of it should be attributed to anthropogenic sources. Hereby any accuracy of anthropogenic impacts, not just for soot, suffers from the limited access to a pre-industrial reference. Anthropogenic uncertainty has a particular strong impact on aerosol indirect effects, which dominate the (TOA) forcing. Accounting for uncertainties in the anthropogenic definition, present-day aerosol forcing is estimated to stay within the −0.7 to −1.6 W/m2 range, with a best estimate at −1 W/m2. Calculations with model predicted temporal changes to anthropogenic AOD indicate that qualitatively the anthropogenic aerosol forcing has not changed much over the last decades and is not likely to increase over the next decades, despite strong regional shifts. These regional shifts explain most solar insolation (brightening or dimming) trends that have been observed by ground-based radiation data.


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