scholarly journals Modelled and observed changes in aerosols and surface solar radiation over Europe between 1960 and 2009

2015 ◽  
Vol 15 (9) ◽  
pp. 13457-13513 ◽  
Author(s):  
S. T. Turnock ◽  
D. V. Spracklen ◽  
K. S. Carslaw ◽  
G. W. Mann ◽  
M. T. Woodhouse ◽  
...  
Keyword(s):  
Solar Radiation ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Radiative Forcing ◽  
Sulfate Aerosol ◽  
Anthropogenic Aerosols ◽  
Surface Solar Radiation ◽  
Aerosol Mass ◽  
The Impact ◽  
Aerosol Radiative

Abstract. Substantial changes in anthropogenic aerosols and precursor gas emissions have occurred over recent decades due to the implementation of air pollution control legislation and economic growth. The response of atmospheric aerosols to these changes and the impact on climate are poorly constrained, particularly in studies using detailed aerosol chemistry climate models. Here we compare the HadGEM3-UKCA coupled chemistry-climate model for the period 1960 to 2009 against extensive ground based observations of sulfate aerosol mass (1978–2009), total suspended particle matter (SPM, 1978–1998), PM10 (1997–2009), aerosol optical depth (AOD, 2000–2009) and surface solar radiation (SSR, 1960–2009) over Europe. The model underestimates observed sulfate aerosol mass (normalised mean bias factor (NMBF) = −0.4), SPM (NMBF = −0.9), PM10 (NMBF = −0.2) and aerosol optical depth (AOD, NMBF = −0.01) but slightly overpredicts SSR (NMBF = 0.02). Trends in aerosol over the observational period are well simulated by the model, with observed (simulated) changes in sulfate of −68% (−78%), SPM of −42% (−20%), PM10 of −9% (−8%) and AOD of −11% (−14%). Discrepancies in the magnitude of simulated aerosol mass do not affect the ability of the model to reproduce the observed SSR trends. The positive change in observed European SSR (5%) during 1990–2009 ("brightening") is better reproduced by the model when aerosol radiative effects (ARE) are included (3%), compared to simulations where ARE are excluded (0.2%). The simulated top-of-the-atmosphere aerosol radiative forcing over Europe under all-sky conditions increased by 3 W m−2 during the period 1970–2009 in response to changes in anthropogenic emissions and aerosol concentrations.

scholarly journals Modelled and observed changes in aerosols and surface solar radiation over Europe between 1960 and 2009

2015 ◽  
Vol 15 (16) ◽  
pp. 9477-9500 ◽  
Author(s):  
S. T. Turnock ◽  
D. V. Spracklen ◽  
K. S. Carslaw ◽  
G. W. Mann ◽  
M. T. Woodhouse ◽  
...  
Keyword(s):  
Solar Radiation ◽  
Radiative Forcing ◽  
Climate Model ◽  
Suspended Particle ◽  
Sulfate Aerosol ◽  
Anthropogenic Aerosols ◽  
Surface Solar Radiation ◽  
Aerosol Mass ◽  
The Impact ◽  
Aerosol Radiative

Abstract. Substantial changes in anthropogenic aerosols and precursor gas emissions have occurred over recent decades due to the implementation of air pollution control legislation and economic growth. The response of atmospheric aerosols to these changes and the impact on climate are poorly constrained, particularly in studies using detailed aerosol chemistry–climate models. Here we compare the HadGEM3-UKCA (Hadley Centre Global Environment Model-United Kingdom Chemistry and Aerosols) coupled chemistry–climate model for the period 1960–2009 against extensive ground-based observations of sulfate aerosol mass (1978–2009), total suspended particle matter (SPM, 1978–1998), PM10 (1997–2009), aerosol optical depth (AOD, 2000–2009), aerosol size distributions (2008–2009) and surface solar radiation (SSR, 1960–2009) over Europe. The model underestimates observed sulfate aerosol mass (normalised mean bias factor (NMBF) = −0.4), SPM (NMBF = −0.9), PM10 (NMBF = −0.2), aerosol number concentrations (N30 NMBF = −0.85; N50 NMBF = −0.65; and N100 NMBF = −0.96) and AOD (NMBF = −0.01) but slightly overpredicts SSR (NMBF = 0.02). Trends in aerosol over the observational period are well simulated by the model, with observed (simulated) changes in sulfate of −68 % (−78 %), SPM of −42 % (−20 %), PM10 of −9 % (−8 %) and AOD of −11 % (−14 %). Discrepancies in the magnitude of simulated aerosol mass do not affect the ability of the model to reproduce the observed SSR trends. The positive change in observed European SSR (5 %) during 1990–2009 ("brightening") is better reproduced by the model when aerosol radiative effects (ARE) are included (3 %), compared to simulations where ARE are excluded (0.2 %). The simulated top-of-the-atmosphere aerosol radiative forcing over Europe under all-sky conditions increased by > 3.0 W m−2 during the period 1970–2009 in response to changes in anthropogenic emissions and aerosol concentrations.

The Impact of Dust Storms on Aerosol Optical Depth and Radiative Forcing

2020 ◽  
Vol 16 (1) ◽  
pp. 1-14
Author(s):  
Monim Jiboori ◽  
Nadia Abed ◽  
Mohamed Abdel Wahab
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Radiative Forcing ◽  
Dust Storms ◽  
The Impact

scholarly journals Radiative forcing estimates of sulfate aerosol in coupled climate-chemistry models with emphasis on the role of the temporal variability

2012 ◽  
Vol 12 (12) ◽  
pp. 5583-5602 ◽  
Author(s):  
C. Déandreis ◽  
Y. Balkanski ◽  
J. L. Dufresne ◽  
A. Cozic
Keyword(s):  
Temporal Variability ◽  
Radiative Forcing ◽  
Climate Model ◽  
Circulation Model ◽  
Reference Method ◽  
Sulfate Aerosol ◽  
The Impact ◽  
Net Fluxes ◽  
Indirect Radiative Forcing ◽  
Aerosol Radiative

Abstract. This paper describes the impact on the sulfate aerosol radiative effects of coupling the radiative code of a global circulation model with a chemistry-aerosol module. With this coupling, temporal variations of sulfate aerosol concentrations influence the estimate of aerosol radiative impacts. Effects of this coupling have been assessed on net fluxes, radiative forcing and temperature for the direct and first indirect effects of sulfate. The direct effect respond almost linearly to rapid changes in concentrations whereas the first indirect effect shows a strong non-linearity. In particular, sulfate temporal variability causes a modification of the short wave net fluxes at the top of the atmosphere of +0.24 and +0.22 W m−2 for the present and preindustrial periods, respectively. This change is small compared to the value of the net flux at the top of the atmosphere (about 240 W m−2). The effect is more important in regions with low-level clouds and intermediate sulfate aerosol concentrations (from 0.1 to 0.8 μg (SO4) m−3 in our model). The computation of the aerosol direct radiative forcing is quite straightforward and the temporal variability has little effect on its mean value. In contrast, quantifying the first indirect radiative forcing requires tackling technical issues first. We show that the preindustrial sulfate concentrations have to be calculated with the same meteorological trajectory used for computing the present ones. If this condition is not satisfied, it introduces an error on the estimation of the first indirect radiative forcing. Solutions are proposed to assess radiative forcing properly. In the reference method, the coupling between chemistry and climate results in a global average increase of 8% in the first indirect radiative forcing. This change reaches 50% in the most sensitive regions. However, the reference method is not suited to run long climate simulations. We present other methods that are simpler to implement in a coupled chemistry/climate model and that offer the possibility to assess radiative forcing.

Aerosol Radiative Forcing and Forcing Efficiency in the UVB for Regions Affected by Saharan and Asian Mineral Dust

2009 ◽  
Vol 66 (4) ◽  
pp. 1033-1040 ◽  
Author(s):  
O. E. García ◽  
A. M. Díaz ◽  
F. J. Expósito ◽  
J. P. Díaz ◽  
A. Redondas ◽  
...  
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Radiative Forcing ◽  
Climate Model ◽  
Mineral Dust ◽  
Global Climate ◽  
Global Climate Model ◽  
Aerosol Radiative Forcing ◽  
Benchmark Database ◽  
Aerosol Radiative

Abstract The influence of mineral dust on ultraviolet energy transfer is studied for two different mineralogical origins. The aerosol radiative forcing ΔF and the forcing efficiency at the surface ΔFeff in the range 290–325 nm were estimated in ground-based stations affected by the Saharan and Asian deserts during the dusty seasons. UVB solar measurements were taken from the World Ozone and Ultraviolet Data Center (WOUDC) for four Asian stations (2000–04) and from the Santa Cruz Observatory, Canary Islands (2002–03), under Gobi and Sahara Desert influences, respectively. The Moderate Resolution Imaging Spectroradiometer (MODIS) aerosol optical depth at 550 nm was used to characterize the aerosol load τ, whereas the aerosol index provided by the Total Ozone Mapping Spectrometer (TOMS) sensor was employed to identify the mineral dust events. The ΔF is strongly affected by the aerosol load, the values found being comparable in both regions during the dusty seasons. Under those conditions, ΔF values as large as −1.29 ± 0.53 W m−2 (τ550 = 0.48 ± 0.24) and −1.43 ± 0.38 W m−2 (τ550 = 0.54 ± 0.26) were reached under Saharan and Asian dust conditions, respectively. Nevertheless, significant differences have been observed in the aerosol radiative forcing per unit of aerosol optical depth in the slant path, τS. The maximum ΔFeff values associated with dust influences were −1.55 ± 0.20 W m−2 τS550−1 for the Saharan region and −0.95 ± 0.11 W m−2 τS550−1 in the Asian area. These results may be used as a benchmark database for establishing aerosol corrections in UV satellite products or in global climate model estimations.

Trends in sulfate and organic aerosol mass in the Southeast U.S.: Impact on aerosol optical depth and radiative forcing

2014 ◽  
Vol 41 (21) ◽  
pp. 7701-7709 ◽  
Author(s):  
A. R. Attwood ◽  
R. A. Washenfelder ◽  
C. A. Brock ◽  
W. Hu ◽  
K. Baumann ◽  
...  
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Radiative Forcing ◽  
Organic Aerosol ◽  
Aerosol Mass

scholarly journals Description and evaluation of aerosol in UKESM1 and HadGEM3-GC3.1 CMIP6 historical simulations

2020 ◽  
Vol 13 (12) ◽  
pp. 6383-6423
Author(s):  
Jane P. Mulcahy ◽  
Colin Johnson ◽  
Colin G. Jones ◽  
Adam C. Povey ◽  
Catherine E. Scott ◽  
...  
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Dimethyl Sulfide ◽  
Cloud Droplet ◽  
Organic Aerosol ◽  
Tropospheric Chemistry ◽  
Earth System ◽  
Aerosol Mass ◽  
The Impact ◽  
Aerosol Source

Abstract. We document and evaluate the aerosol schemes as implemented in the physical and Earth system models, the Global Coupled 3.1 configuration of the Hadley Centre Global Environment Model version 3 (HadGEM3-GC3.1) and the United Kingdom Earth System Model (UKESM1), which are contributing to the sixth Coupled Model Intercomparison Project (CMIP6). The simulation of aerosols in the present-day period of the historical ensemble of these models is evaluated against a range of observations. Updates to the aerosol microphysics scheme are documented as well as differences in the aerosol representation between the physical and Earth system configurations. The additional Earth system interactions included in UKESM1 lead to differences in the emissions of natural aerosol sources such as dimethyl sulfide, mineral dust and organic aerosol and subsequent evolution of these species in the model. UKESM1 also includes a stratospheric–tropospheric chemistry scheme which is fully coupled to the aerosol scheme, while GC3.1 employs a simplified aerosol chemistry mechanism driven by prescribed monthly climatologies of the relevant oxidants. Overall, the simulated speciated aerosol mass concentrations compare reasonably well with observations. Both models capture the negative trend in sulfate aerosol concentrations over Europe and the eastern United States of America (US) although the models tend to underestimate sulfate concentrations in both regions. Interactive emissions of biogenic volatile organic compounds in UKESM1 lead to an improved agreement of organic aerosol over the US. Simulated dust burdens are similar in both models despite a 2-fold difference in dust emissions. Aerosol optical depth is biased low in dust source and outflow regions but performs well in other regions compared to a number of satellite and ground-based retrievals of aerosol optical depth. Simulated aerosol number concentrations are generally within a factor of 2 of the observations, with both models tending to overestimate number concentrations over remote ocean regions, apart from at high latitudes, and underestimate over Northern Hemisphere continents. Finally, a new primary marine organic aerosol source is implemented in UKESM1 for the first time. The impact of this new aerosol source is evaluated. Over the pristine Southern Ocean, it is found to improve the seasonal cycle of organic aerosol mass and cloud droplet number concentrations relative to GC3.1 although underestimations in cloud droplet number concentrations remain. This paper provides a useful characterisation of the aerosol climatology in both models and will facilitate understanding in the numerous aerosol–climate interaction studies that will be conducted as part of CMIP6 and beyond.

scholarly journals Aerosol radiative forcings induced by substantial changes in anthropogenic emissions in China from 2008 to 2016

2021 ◽  
Vol 21 (8) ◽  
pp. 5965-5982
Author(s):  
Mingxu Liu ◽  
Hitoshi Matsui
Keyword(s):  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Radiative Forcing ◽  
Eastern China ◽  
Radiation Budget ◽  
Anthropogenic Emissions ◽  
Radiative Forcings ◽  
The Past ◽  
Positive Direct ◽  
Aerosol Radiative

Abstract. Anthropogenic emissions in China play an important role in altering the global radiation budget. Over the past decade, the strong clean-air policies in China have resulted in substantial reductions of anthropogenic emissions of sulfur dioxide (SO2) and primary particulate matter, and air quality in China has consequently improved. However, the resultant aerosol radiative forcings have been poorly understood. In this study, we used an advanced global climate model integrated with the latest localized emission inventory to quantify the aerosol radiative forcings by the changes of anthropogenic emissions in China between 2008 and 2016. By comparing with multiple observation datasets, our simulations reproduced the considerable reductions of sulfate and black carbon (BC) mass loadings reasonably well over eastern China (the key region subject to stringent emission controls) during the period and accordingly showed a clear decline in both aerosol optical depth and absorption aerosol optical depth. The results revealed a regional annual mean positive direct radiative forcing (DRF) of +0.29 W m−2 at the top of the atmosphere (TOA) due to the reduction of SO2 emissions. This positive aerosol radiative forcing was comprised of diminished sulfate scattering (+0.58 W m−2), enhanced nitrate radiative effects (−0.29 W m−2), and could be completely offset by the concurrent reduction of BC emissions that induced a negative BC DRF of −0.33 W m−2. Despite the small net aerosol DRF (−0.05 W m−2) at the TOA, aerosol–radiation interactions could explain the surface brightening in China over the past decade. The overall reductions in aerosol burdens and associated optical effects mainly from BC and sulfate enhanced the regional annual mean downward solar radiation flux at the surface by +1.0 W m−2 between 2008 and 2016. The enhancement was in general agreement with a long-term observational record of surface energy fluxes in China. We also estimated that aerosol effects on cloud radiative forcings may have played a dominant role in the net aerosol radiative forcings at the TOA in China and over the northern Pacific Ocean during the study period. This study will facilitate more informed assessment of climate responses to projected emissions in the future as well as to sudden changes in human activities (e.g., the COVID-19 lockdown).

scholarly journals Analysis on the impact of aerosol optical depth on surface solar radiation in the Shanghai megacity, China

2011 ◽  
Vol 11 (7) ◽  
pp. 3281-3289 ◽  
Author(s):  
J. Xu ◽  
C. Li ◽  
H. Shi ◽  
Q. He ◽  
L. Pan
Keyword(s):  
Solar Radiation ◽  
Aerosol Optical Depth ◽  
Optical Depth ◽  
Decadal Variation ◽  
Surface Solar Radiation ◽  
Atmospheric Transparency ◽  
Clear Sky ◽  
Term Variation ◽  
Sky Conditions

Abstract. This study investigated the decadal variation of the direct surface solar radiation (DiSR) and the diffuse surface solar radiation (DfSR) during 1961–2008 in the Shanghai megacity as well as their relationships to Aerosol Optical Depth (AOD) under clear-sky conditions. Three successive periods with unique features of long term variation of DiSR were identified for both clear-sky and all-sky conditions: a "dimming" period from the late 1960s to the mid 1980s, a "stabilization"/"slight brightening" period from the mid 1980s to the mid 1990s, and a "renewed dimming" period thereafter. During the two dimming periods of DiSR, DfSR brightened significantly under clear-sky conditions, indicating that change in atmospheric transparency resulting from aerosol emission has an important role on decadal variation of surface solar radiation (SSR) over this area. The analysis on the relationship between the Moderate-resolution Imaging Spectroradiometer (MODIS) retrieved AOD and the corresponding hourly measurements of DiSR and DfSR under clear-sky conditions clearly revealed that AOD is significantly correlated and anti-correlated with DfSR and DiSR, respectively, both above 99% confidence in all seasons, indicating the great impact of aerosols on SSR through absorption and/or scattering in the atmosphere. In addition, both AOD and the corresponding DiSR and DfSR measured during the satellite passage over Shanghai show obvious weekly cycles. On weekends, AOD is lower than the weekly average, corresponding to higher DiSR and lower DfSR, while the opposite pattern was true for weekdays. Less AOD on weekends due to the reduction of transportation and industrial activities results in enhancement of atmospheric transparency under cloud free conditions so as to increase DiSR and decrease DfSR simultaneously. Results show that aerosol loading from the anthropogenic emissions is an important modulator for the long term variation of SSR in Shanghai.

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