scholarly journals Global fine-mode aerosol radiative effect, as constrained by comprehensive observations

2016 ◽  
Vol 16 (13) ◽  
pp. 8071-8080 ◽  
Author(s):  
Chul E. Chung ◽  
Jung-Eun Chu ◽  
Yunha Lee ◽  
Twan van Noije ◽  
Hwayoung Jeoung ◽  
...  

Abstract. Aerosols directly affect the radiative balance of the Earth through the absorption and scattering of solar radiation. Although the contributions of absorption (heating) and scattering (cooling) of sunlight have proved difficult to quantify, the consensus is that anthropogenic aerosols cool the climate, partially offsetting the warming by rising greenhouse gas concentrations. Recent estimates of global direct anthropogenic aerosol radiative forcing (i.e., global radiative forcing due to aerosol–radiation interactions) are −0.35 ± 0.5 W m−2, and these estimates depend heavily on aerosol simulation. Here, we integrate a comprehensive suite of satellite and ground-based observations to constrain total aerosol optical depth (AOD), its fine-mode fraction, the vertical distribution of aerosols and clouds, and the collocation of clouds and overlying aerosols. We find that the direct fine-mode aerosol radiative effect is −0.46 W m−2 (−0.54 to −0.39 W m−2). Fine-mode aerosols include sea salt and dust aerosols, and we find that these natural aerosols result in a very large cooling (−0.44 to −0.26 W m−2) when constrained by observations. When the contribution of these natural aerosols is subtracted from the fine-mode radiative effect, the net becomes −0.11 (−0.28 to +0.05) W m−2. This net arises from total (natural + anthropogenic) carbonaceous, sulfate and nitrate aerosols, which suggests that global direct anthropogenic aerosol radiative forcing is less negative than −0.35 W m−2.

2016 ◽  
Author(s):  
Chul E. Chung ◽  
Jung-Eun Chu ◽  
Yunha Lee ◽  
Twan van Noije ◽  
Hwayoung Jeoung ◽  
...  

Abstract. Aerosols directly affect the radiative balance of the Earth through absorption and scattering of solar radiation. Although the contributions of absorption (heating) and scattering (cooling) of sunlight have proved difficult to quantify, the consensus is that anthropogenic aerosols cool the climate, partially offsetting the warming by rising greenhouse gas concentrations. Recent estimates of global direct aerosol radiative forcing are −0.35 ± 0.5 Wm−2, and these estimates depend either entirely or heavily on aerosol simulation. Here, we integrate a comprehensive suite of satellite and ground-based observations to constrain total AOD, its fine-mode fraction, the vertical distribution of aerosols and clouds, and the co-location of clouds and overlying aerosols. We find that fine-mode forcing is −0.46 Wm−2 (−0.54 ~ −0.39 Wm−2). Fine-mode aerosols include sea salt and dust aerosols, and we find that these natural aerosols pose a very large cooling (−0.44 ~ −0.26 Wm−2) when constrained by observations. When the contribution of these natural aerosols is subtracted from the fine-mode forcing, the net becomes −0.10 (−0.28 ~ +0.05) Wm−2. The net forcing arises from carbonaceous, sulfate and nitrate aerosols. Despite uncertainties in the anthropogenic fraction of these aerosols, this −0.28 ~ +0.05 Wm−2 range compels the direct aerosol forcing to be near zero.


2016 ◽  
Vol 113 (43) ◽  
pp. 12053-12058 ◽  
Author(s):  
Hamish Gordon ◽  
Kamalika Sengupta ◽  
Alexandru Rap ◽  
Jonathan Duplissy ◽  
Carla Frege ◽  
...  

The magnitude of aerosol radiative forcing caused by anthropogenic emissions depends on the baseline state of the atmosphere under pristine preindustrial conditions. Measurements show that particle formation in atmospheric conditions can occur solely from biogenic vapors. Here, we evaluate the potential effect of this source of particles on preindustrial cloud condensation nuclei (CCN) concentrations and aerosol–cloud radiative forcing over the industrial period. Model simulations show that the pure biogenic particle formation mechanism has a much larger relative effect on CCN concentrations in the preindustrial atmosphere than in the present atmosphere because of the lower aerosol concentrations. Consequently, preindustrial cloud albedo is increased more than under present day conditions, and therefore the cooling forcing of anthropogenic aerosols is reduced. The mechanism increases CCN concentrations by 20–100% over a large fraction of the preindustrial lower atmosphere, and the magnitude of annual global mean radiative forcing caused by changes of cloud albedo since 1750 is reduced by 0.22 W m−2 (27%) to −0.60 W m−2. Model uncertainties, relatively slow formation rates, and limited available ambient measurements make it difficult to establish the significance of a mechanism that has its dominant effect under preindustrial conditions. Our simulations predict more particle formation in the Amazon than is observed. However, the first observation of pure organic nucleation has now been reported for the free troposphere. Given the potentially significant effect on anthropogenic forcing, effort should be made to better understand such naturally driven aerosol processes.


2013 ◽  
Vol 13 (11) ◽  
pp. 29685-29720 ◽  
Author(s):  
H. Che ◽  
X. Xia ◽  
J. Zhu ◽  
Z. Li ◽  
O. Dubovic ◽  
...  

Abstract. In January 2013, North China Plain experienced several serious haze events. Cimel sunphotometer measurements at seven sites over rural, suburban and urban regions of North China Plain from 1 to 30 January 2013 were used to further our understanding of spatial-temporal variation of aerosol optical parameters and aerosol radiative forcing (ARF). It was found that Aerosol Optical Depth at 500 nm (AOD500 nm) during non-pollution periods at all stations was lower than 0.30 and increased significantly to greater than 1.00 as pollution events developed. The Angstrom exponent (Alpha) was larger than 0.80 for all stations most of the time. AOD500 nm averages increased from north to south during both polluted and non-polluted periods on the three urban sites in Beijing. The fine mode AOD during pollution periods is about a factor of 2.5 times larger than that during the non-pollution period at urban sites but a factor of 5.0 at suburban and rural sites. The fine mode fraction of AOD675 nm was higher than 80% for all sites during January 2013. The absorption AOD675 nm at rural sites was only about 0.01 during pollution periods, while ~0.03–0.07 and 0.01–0.03 during pollution and non-pollution periods at other sites, respectively. Single scattering albedo varied between 0.87 and 0.95 during January 2013 over North China Plain. The size distribution showed an obvious tri-peak pattern during the most serious period. The fine mode effective radius in the pollution period was about 0.01–0.08 μm larger than during non-pollution periods, while the coarse mode radius in pollution periods was about 0.06–0.38 μm less than that during non-pollution periods. The total, fine and coarse mode particle volumes varied by about 0.06–0.34 μm3, 0.03–0.23 μm3, and 0.03–0.10 μm3, respectively, throughout January 2013. During the most intense period (1–16 January), aerosol radiative forcing (ARF) at the surface exceeded −50 W m−2, −180 W m−2, and −200 W m−2 at rural, suburban, and urban sites, respectively. The ARF readings at the top of the atmosphere were approximately −30 W m−2 in rural and −40–60 W m−2 in urban areas. Positive ARF at the top of the atmosphere at the Huimin suburban site was found to be different from others as a result of the high surface albedo due to snow cover.


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.


2017 ◽  
Vol 10 (1) ◽  
pp. 433-452 ◽  
Author(s):  
Bjorn Stevens ◽  
Stephanie Fiedler ◽  
Stefan Kinne ◽  
Karsten Peters ◽  
Sebastian Rast ◽  
...  

Abstract. A simple plume implementation of the second version (v2) of the Max Planck Institute Aerosol Climatology, MACv2-SP, is described. MACv2-SP provides a prescription of anthropogenic aerosol optical properties and an associated Twomey effect. It was created to provide a harmonized description of post-1850 anthropogenic aerosol radiative forcing for climate modeling studies. MACv2-SP has been designed to be easy to implement, change and use, and thereby enable studies exploring the climatic effects of different patterns of aerosol radiative forcing, including a Twomey effect. MACv2-SP is formulated in terms of nine spatial plumes associated with different major anthropogenic source regions. The shape of the plumes is fit to the Max Planck Institute Aerosol Climatology, version 2, whose present-day (2005) distribution is anchored by surface-based observations. Two types of plumes are considered: one predominantly associated with biomass burning, the other with industrial emissions. These differ in the prescription of their annual cycle and in their optical properties, thereby implicitly accounting for different contributions of absorbing aerosol to the different plumes. A Twomey effect for each plume is prescribed as a change in the host model's background cloud-droplet population density using relationships derived from satellite data. Year-to-year variations in the amplitude of the plumes over the historical period (1850–2016) are derived by scaling the plumes with associated national emission sources of SO2 and NH3. Experiments using MACv2-SP are performed with the Max Planck Institute Earth System Model. The globally and annually averaged instantaneous and effective aerosol radiative forcings are estimated to be −0.6 and −0.5 W m−2, respectively. Forcing from aerosol–cloud interactions (the Twomey effect) offsets the reduction of clear-sky forcing by clouds, so that the net effect of clouds on the aerosol forcing is small; hence, the clear-sky forcing, which is more readily measurable, provides a good estimate of the total aerosol forcing.


2014 ◽  
Vol 92 ◽  
pp. 250-266 ◽  
Author(s):  
Yi Gao ◽  
Chun Zhao ◽  
Xiaohong Liu ◽  
Meigen Zhang ◽  
L. Ruby Leung

2021 ◽  
Author(s):  
Matthew Christensen ◽  
Andrew Gettelman ◽  
Jan Cermak ◽  
Guy Dagan ◽  
Michael Diamond ◽  
...  

Abstract. Aerosol-cloud interactions (ACI) are considered to be the most uncertain driver of present-day radiative forcing due to human activities. The non-linearity of cloud-state changes to aerosol perturbations make it challenging to attribute causality in observed relationships of aerosol radiative forcing. Using correlations to infer causality can also be challenging when meteorological variability also drives both aerosol and cloud changes independently. Natural and anthropogenic aerosol perturbations from well defined sources provide “opportunistic experiments” (also known as natural experiments) to investigate ACI in cases where causality may be more confidently inferred. These perturbations cover a wide range of locations and spatio-temporal scales, including point sources such as volcanic eruptions or industrial sources, plumes from biomass burning or forest fires, and tracks from individual ships or shipping corridors. We review the different experimental conditions and conduct a synthesis of the available satellite data sets and field campaigns to place these opportunistic experiments on a common footing, facilitating new insights and a clearer understanding of key uncertainties in aerosol radiative forcing. Strong liquid water path increases due to aerosol perturbations are largely ruled out by averaging across experiments. Cloud albedo perturbations are strongly sensitive to background meteorological conditions. Opportunistic experiments have significantly improved process level understanding of ACI, but it remains unclear how reliably the relationships found can be scaled to the global level, thus, demonstrating a need for deeper investigation in order to improve assessments of aerosol radiative forcing and climate change.


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.


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