Shortwave Direct Radiative Effect Research Articles

Satellite-based analysis of top of atmosphere shortwave radiative forcing trend induced by biomass burning aerosols over South-Eastern Atlantic

This study investigates long-term changes in the shortwave direct aerosol radiative effect (DARE) at the top of the atmosphere (TOA) induced by biomass burning aerosol (BBA) transported from southern Africa to the south-eastern Atlantic (SEA) stratocumulus region during extended fire seasons. The evolution since 2002 of aerosol, cloud properties, and TOA shortwave outgoing radiation from advanced passive satellite sensors are presented, as well as the observational trend in clear-sky DAREclr and the retrieval trend in all-sky DAREall. Supplemented by chemical transport model simulations, we estimate that DAREclr has become more negative (−0.09 ± 0.06 W m−2 yr−1) due to increased aerosol presence in SEA. Meanwhile, DAREall has become more positive ( + 0.04 ± 0.15 W m−2 yr−1) due to aerosols in cloudy sky regions. This study reveals satellite capabilities in capturing complex BBA-cloud-solar radiation interactions for accurate radiative forcing estimates and projections.

Assessing Lidar Ratio Impact on CALIPSO Retrievals Utilized for the Estimation of Aerosol SW Radiative Effects across North Africa, the Middle East, and Europe

North Africa, the Middle East, and Europe (NAMEE domain) host a variety of suspended particles characterized by different optical and microphysical properties. In the current study, we investigate the importance of the lidar ratio (LR) on Cloud-Aerosol Lidar with Orthogonal Polarization–Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observations (CALIOP-CALIPSO) aerosol retrievals towards assessing aerosols’ impact on the Earth-atmosphere radiation budget. A holistic approach has been adopted involving collocated Aerosol Robotic Network (AERONET) observations, Radiative Transfer Model (RTM) simulations, as well as reference radiation measurements acquired using spaceborne (Clouds and the Earth’s Radiant Energy System-CERES) and ground-based (Baseline Surface Radiation Network-BSRN) instruments. We are assessing the clear-sky shortwave (SW) direct radiative effects (DREs) on 550 atmospheric scenes, identified within the 2007–2020 period, in which the primary tropospheric aerosol species (dust, marine, polluted continental/smoke, elevated smoke, and clean continental) are probed using CALIPSO. RTM runs have been performed relying on CALIOP retrievals in which the default and the DeLiAn (Depolarization ratio, Lidar ratio, and Ångström exponent)-based aerosol-speciated LRs are considered. The simulated fields from both configurations are compared against those produced when AERONET AODs are applied. Overall, the DeLiAn LRs leads to better results mainly when mineral particles are either solely recorded or coexist with other aerosol species (e.g., sea-salt). In quantitative terms, the errors in DREs are reduced by ~26–27% at the surface (from 5.3 to 3.9 W/m2) and within the atmosphere (from −3.3 to −2.4 W/m2). The improvements become more significant (reaching up to ~35%) for moderate-to-high aerosol loads (AOD ≥ 0.2).

Sensitivity of global direct aerosol shortwave radiative forcing to uncertainties in aerosol optical properties

Abstract. New satellite missions promise global reductions in the uncertainties in aerosol optical properties, but it is unclear how those reductions will propagate to uncertainties in the shortwave (SW) direct aerosol radiative effect (DARE) and direct aerosol radiative forcing (DARF), which are currently large, on the order of at least 20 %. In this work, we build a Monte Carlo framework to calculate the impact of uncertainties in aerosol optical depth (AOD), single scattering albedo (SSA), and the asymmetry parameter on the uncertainty in shortwave DARE and DARF. This framework uses the results of over 2.3 million radiative transfer simulations to calculate global clear-sky DARE and DARF based on a range of uncertainties in present-day and pre-industrial aerosol optical properties, representative of existing and future global observing systems. We find the 1σ uncertainty varies between ±0.23 and ±1.91 W m−2 (5 % and 42 %) for the top-of-atmosphere (TOA) clear-sky DARE and between ±0.08 and ±0.47 W m−2 (9 % and 52 %) for the TOA DARF. At the TOA, AOD uncertainty is the main contributor to overall uncertainty except over bright surfaces where SSA uncertainty contributes most. We apply regionally varying uncertainties to represent current measurement uncertainties and find that aerosol optical property uncertainties represent 24 % of TOA DARE and DARF. Reducing regionally varying optical property uncertainties by a factor of 2 would reduce their contributions to TOA DARE and DARF uncertainty proportionally. Applying a simple scaling to all-sky conditions, aerosol optical property uncertainty contributes to about 25 % total uncertainty in TOA, all-sky SW DARE, and DARF. Compared to previous studies which considered uncertainties in non-aerosol variables, our results suggest that the aerosol optical property uncertainty accounts for one-third to half of the total direct SW uncertainty. Recent and future progress in constraining aerosol optical properties using ground-based or satellite retrievals could be translated into DARE and DARF uncertainty using our freely available framework.

Global 3-D distribution of aerosol composition by synergistic use of CALIOP and MODIS observations

Abstract. For the observation of the global three-dimensional distribution of aerosol composition and the evaluation of the shortwave direct radiative effect (SDRE) by aerosols, we developed a retrieval algorithm that uses observation data from the Cloud–Aerosol Lidar with Orthogonal Polarization (CALIOP) on board the Cloud–Aerosol Lidar Infrared Pathfinder Satellite Observations (CALIPSO) satellite and the Moderate Resolution Imaging Spectroradiometer (MODIS) on board Aqua. The CALIOP–MODIS retrieval optimizes the aerosol composition to both the CALIOP and MODIS observations in the daytime. Aerosols were assumed to be composed of four aerosol components: water-soluble (WS), light-absorbing (LA), dust (DS), and sea salt (SS) particles. The outputs of the CALIOP–MODIS retrieval are the vertical profiles of the extinction coefficient (αa), single-scattering albedo (ω0), asymmetry factor (g) of total aerosols (WS+LA+DS+SS), and αa of WS, LA, DS, and SS. Daytime observations of CALIOP and MODIS in 2010 were analyzed by the CALIOP–MODIS retrieval. The global means of the aerosol optical depth (τa) at 532 nm were 0.147±0.148 for total aerosols, 0.072±0.085 for WS, 0.027±0.035 for LA, 0.025±0.054 for DS, and 0.023±0.020 for SS. τa of the CALIOP–MODIS retrieval was between those of the CALIPSO and MODIS standard products and was close to the MODIS standard product. The global means of ω0 and g were 0.940±0.038 and 0.718±0.037; these values are in the range of those reported by previous studies. The horizontal distribution of each aerosol component was reasonable; for example, DS was large in desert regions, and LA was large in the major regions of biomass burning and anthropogenic aerosol emissions. The values of τa, ω0, g, and fine and coarse median radii of the CALIOP–MODIS retrieval were compared with those of the AERONET products. τa at 532 and 1064 nm of the CALIOP–MODIS retrieval agreed well with the AERONET products. The ω0, g, and fine and coarse median radii of the CALIOP–MODIS retrieval were not far from those of the AERONET products, but the variations were large, and the coefficients of determination for linear regression between them were small. In the retrieval results for 2010, the clear-sky SDRE values for total aerosols at the top and bottom of the atmosphere were -4.99±3.42 and -13.10±9.93 W m−2, respectively, and the impact of total aerosols on the heating rate was from 0.0 to 0.5 K d−1. These results are generally similar to those of previous studies, but the SDRE at the bottom of the atmosphere is larger than that reported previously. Consequently, comparison with previous studies showed that the CALIOP–MODIS retrieval results were reasonable with respect to aerosol composition, optical properties, and the SDRE.

A Method to Account for the Impact of Water Vapor on Observation‐Based Estimates of the Clear‐Sky Shortwave Direct Radiative Effect of Mineral Dust

AbstractThe shortwave direct radiative effect of dust, the difference between net shortwave radiative flux in a cloud free and cloud and aerosol free atmosphere, is typically estimated using forward calculations made with a radiative transfer model. However, estimates of the direct radiative effect made via this initial method can be highly uncertain due to difficultly in accurately describing the relevant optical and physical properties of dust used in these calculations. An alternative approach to estimate this effect is to determine the forcing efficiency, or the direct radiative effect normalized by aerosol optical depth. While this approach avoids the uncertainties associated with the initial method for calculating the direct effect, random errors and biases associated with this approach have not been thoroughly examined in literature. Here we explore biases in this observation‐based approach that are related to atmospheric water vapor. We use observations to show that over the Sahara Desert dust optical depth and column‐integrated atmospheric water vapor are positively correlated. We use three idealized radiative models of varying complexity to demonstrate that a positive correlation between dust and water vapor produces a positive bias in the dust forcing efficiency estimated via the observation‐based method. We describe a simple modification to the observation‐based method that correctly accounts for the correlation between dust and water vapor when estimating the forcing efficiency and use this method to estimate the instantaneous forcing efficiency of dust over the Sahara Desert using satellite data, obtaining −12.3 ± 6.68 to 20.9 ± 11.9 W m−2 per unit optical depth.

Aerosol radiative impact during the summer 2019 heatwave produced partly by an inter-continental Saharan dust outbreak – Part 1: Short-wave dust direct radiative effect

Abstract. The short-wave (SW) direct radiative effect (DRE) during the summer 2019 heatwave produced partly by a moderate, long-lasting Saharan dust outbreak over Europe is analysed in this study. Two European sites (periods) are considered: Barcelona, Spain (23–30 June), and Leipzig, Germany (29 and 30 June), 1350 km apart from each other. Major data are obtained from AERONET and polarised Micro-Pulse Lidar (P-MPL) observations. Modelling is used to describe the different dust pathways, as observed at both sites. The coarse dust (Dc) and fine dust (Df) components (with total dust, DD = Dc + Df) are identified in the profiles of the total particle backscatter coefficient using the POLIPHON (POlarisation LIdar PHOtometer Networking) method in synergy with P-MPL measurements. This information is used to calculate the relative mass loading and the centre-of-mass height, as well as the contribution of each dust mode to the total dust DRE. Several aspects of the ageing of dust are put forward. The mean dust optical depth and its Df/DD ratios are, respectively, 0.153 and 24 % in Barcelona and 0.039 and 38 % in Leipzig; this Df increase in Leipzig is attributed to a longer dust transport path in comparison to Barcelona. The dust produced a cooling effect on the surface with a mean daily DRE of −9.1 and −2.5 W m−2, respectively, in Barcelona and Leipzig, but the Df/DD DRE ratio is larger for Leipzig (52 %) than for Barcelona (37 %). Cooling is also observed at the top of the atmosphere (TOA), although less intense than on the surface. However, the Df/DD DRE ratio at the TOA is even higher (45 % and 60 %, respectively, in Barcelona and Leipzig) than on the surface. Despite the predominance of Dc particles under dusty conditions, the SW radiative impact of Df particles can be comparable to, even higher than, that induced by the Dc ones. In particular, the Df/DD DRE ratio in Barcelona increases by +2.4 % d−1 (surface) and +2.9 % d−1 (TOA) during the dusty period. This study is completed by a second paper about the long-wave and net radiative effects. These results are especially relevant for the next ESA EarthCARE mission (planned in 2022) as it is devoted to aerosol–cloud–radiation interaction research.

Unexpected Biomass Burning Aerosol Absorption Enhancement Explained by Black Carbon Mixing State

AbstractDirect and semi‐direct radiative effects of biomass burning aerosols (BBA) from southern and central African fires are still widely debated, in particular because climate models have been unsuccessful in reproducing the low single scattering albedo in BBA over the eastern Atlantic Ocean. Using state‐of‐the‐art airborne in situ measurements and Mie scattering simulations, we demonstrate that low single scattering albedo in well‐aged BBA plumes over southern West Africa results from the presence of strongly absorbing refractory black carbon (rBC), whereas the brown carbon contribution to the BBA absorption is negligible. Coatings enhance light absorption by rBC‐containing particles by up to 210%. Our results show that accounting for the diversity in black carbon mixing state by combining internal and external configurations is needed to accurately estimate the optical properties and henceforth the shortwave direct radiative effect and heating rate of BBA over southern West Africa.

Aerosol-radiation interaction in atmospheric models: Idealized sensitivity study of simulated short-wave direct radiative effects to particle microphysical properties

We assessed the impact of the microphysical parameterization of natural and anthropogenic aerosols on simulated short-wave radiative effects due to Aerosol-Radiation Interaction (ARI). Layer radiative properties (optical depth, single scattering albedo and asymmetry factor) of dry mineral dust, organic carbon and a black carbon-sulfate mixture have been calculated with a T-matrix code in the short-wave spectral region, after perturbing relevant particle microphysical properties (size distribution, refractive index, mixing state). For each aerosol species, an idealized atmospheric layer and three events of increasing intensity have been set. Then, short-wave direct radiative effects (clear-sky) have been simulated at the top-of-atmosphere (TOA) and at surface (SFC) using the radiative transfer model RRTMG_SW (widely used in atmospheric models), separately for each aerosol species. We observed considerably variable impacts of the particle microphysical perturbations on the layer radiative properties for mineral dust and organic carbon, mainly due to the different sizes of the two species. For the black carbon-sulfate mixture, the single scattering albedo has been found to be much lower in the internal mixing case. Regarding the direct radiative effects, we observed perturbation-induced variability ranges (evaluated against the base net fluxes in absence of aerosols) always within the perturbation range set for the particle microphysical properties (±20%→40%). This work, therefore, quantitatively demonstrates that small uncertainties on the aerosol microphysical parameterization propagate on the simulated direct radiative effects mainly with a loss of strength. Considerable perturbation-induced absolute variations of the direct radiative effects have been found (above all for large aerosol amounts), which could significantly affect the model assessments of the ARI radiative effects and therefore meteorological forecasts and climate predictions.

Optical, physical and chemical properties of aerosols transported to a coastal site in the western Mediterranean: a focus on primary marine aerosols

Abstract. As part of the ChArMEx-ADRIMED campaign (summer 2013), ground-based in situ observations were conducted at the Ersa site (northern tip of Corsica; 533 m a.s.l.) to characterise the optical, physical and chemical properties of aerosols. During the observation period, a major influence of primary marine aerosols was detected (22–26 June), with a mass concentration reaching up to 6.5 µg m−3 and representing more than 40 % of the total PM10 mass concentration. Its relatively low ratio of chloride to sodium (average of 0.57) indicates a fairly aged sea salt aerosol at Ersa. In this work, an original data set, obtained from online real-time instruments (ATOFMS, PILS-IC) has been used to characterise the ageing of primary marine aerosols (PMAs). During this PMA period, the mixing of fresh and aged PMAs was found to originate from both local and regional (Gulf of Lion) emissions, according to local wind measurements and FLEXPART back trajectories. Two different aerosol regimes have been identified: a dust outbreak (dust) originating from Algeria/Tunisia, and a pollution period with aerosols originating from eastern Europe, which includes anthropogenic and biomass burning sources (BBP). The optical, physical and chemical properties of the observed aerosols, as well as their local shortwave (SW) direct radiative effect (DRE) in clear-sky conditions, are compared for these three periods in order to assess the importance of the direct radiative impact of PMAs compared to other sources above the western Mediterranean Basin. As expected, AERONET retrievals indicate a relatively low local SW DRF during the PMA period with mean values of −11 ± 4 at the surface and −8 ± 3 W m−2 at the top of the atmosphere (TOA). In comparison, our results indicate that the dust outbreak observed at our site during the campaign, although of moderate intensity (AOD of 0.3–0.4 at 440 nm and column-integrated SSA of 0.90–0.95), induced a local instantaneous SW DRF that is nearly 3 times the effect calculated during the PMA period, with maximum values up to −40 W m−2 at the surface. A similar range of values were found for the BBP period to those during the dust period (SW DRF at the surface and TOA of −23 ± 6 and −15 ± 4 W m−2 respectively). The multiple sources of measurements at Ersa allowed the detection of a PMA-dominant period and their characterisation in terms of ageing, origin, transport, optical and physical properties and direct climatic impact.

Direct radiative effect of aerosols based on PARASOL and OMI satellite observations

AbstractAccurate portrayal of the aerosol characteristics is crucial to determine aerosol contribution to the Earth's radiation budget. We employ novel satellite retrievals to make a new measurement‐based estimate of the shortwave direct radiative effect of aerosols (DREA), both over land and ocean. Global satellite measurements of aerosol optical depth, single‐scattering albedo (SSA), and phase function from PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Sciences coupled with Observations from a Lidar) are used in synergy with OMI (Ozone Monitoring Instrument) SSA. Aerosol information is combined with land‐surface bidirectional reflectance distribution function and cloud characteristics from MODIS (Moderate Resolution Imaging Spectroradiometer) satellite products. Eventual gaps in observations are filled with the state‐of‐the‐art global aerosol model ECHAM5‐HAM2. It is found that our estimate of DREA is largely insensitive to model choice. Radiative transfer calculations show that DREA at top‐of‐atmosphere is −4.6 ± 1.5 W/m2 for cloud‐free and −2.1 ± 0.7 W/m2 for all‐sky conditions, during year 2006. These fluxes are consistent with, albeit generally less negative over ocean than, former assessments. Unlike previous studies, our estimate is constrained by retrievals of global coverage SSA, which may justify different DREA values. Remarkable consistency is found in comparison with DREA based on CERES (Clouds and the Earth's Radiant Energy System) and MODIS observations.

Comparison of key absorption and optical properties between pure and transported anthropogenic dust over East and Central Asia

Abstract. Asian dust particulate is one of the primary aerosol constituents in the Earth–atmosphere system that exerts profound influences on environmental quality, human health, the marine biogeochemical cycle, and Earth's climate. To date, the absorptive capacity of dust aerosol generated from the Asian desert region is still an open question. In this article, we compile columnar key absorption and optical properties of mineral dust over East and Central Asian areas by utilizing the multiyear quality-assured datasets observed at 13 sites of the Aerosol Robotic Network (AERONET). We identify two types of Asian dust according to threshold criteria from previously published literature. (1) The particles with high aerosol optical depth at 440 nm (AOD440 ≥ 0.4) and a low Ångström wavelength exponent at 440–870 nm (α < 0.2) are defined as Pure Dust (PDU), which decreases disturbance of other non-dust aerosols and keeps high accuracy of pure Asian dust. (2) The particles with AOD440 ≥ 0.4 and 0.2 < α < 0.6 are designated as Transported Anthropogenic Dust (TDU), which is mainly dominated by dust aerosol and might mix with other anthropogenic aerosol types. Our results reveal that the primary components of high AOD days are predominantly dust over East and Central Asian regions, even if their variations rely on different sources, distance from the source, emission mechanisms, and meteorological characteristics. The overall mean and standard deviation of single-scattering albedo, asymmetry factor, real part and imaginary part of complex refractive index at 550 nm for Asian PDU are 0.935 ± 0.014, 0.742 ± 0.008, 1.526 ± 0.029, and 0.00226 ± 0.00056, respectively, while corresponding values are 0.921 ± 0.021, 0.723 ± 0.009, 1.521 ± 0.025, and 0.00364 ± 0.0014 for Asian TDU. Aerosol shortwave direct radiative effects at the top of the atmosphere (TOA), at the surface (SFC), and in the atmospheric layer (ATM) for Asian PDU (α < 0.2) and TDU (0.2 < α < 0.6) computed in this study, are a factor of 2 smaller than the results of Optical Properties of Aerosols and Clouds (OPAC) mineral-accumulated (mineral-acc.) and mineral-transported (mineral-tran.) modes. Therefore, we are convinced that our results hold promise for updating and improving accuracies of Asian dust characteristics in present-day remote sensing applications and regional or global climate models.

Continental pollution in the Western Mediterranean basin: large variability of the aerosol single scattering albedo and influence on the direct shortwave radiative effect

Abstract. Pollution aerosols strongly influence the composition of the Western Mediterranean basin, but at present little is known on their optical properties. We report in this study in situ observations of the single scattering albedo (ω) of pollution aerosol plumes measured over the Western Mediterranean basin during the TRAQA (TRansport and Air QuAlity) airborne campaign in summer 2012. Cases of pollution export from different source regions around the basin and at different altitudes between ∼ 160 and 3500 m above sea level were sampled during the flights. Data from this study show a large variability of ω, with values between 0.84–0.98 at 370 nm and 0.70–0.99 at 950 nm. The single scattering albedo generally decreases with the wavelength, with some exception associated to the mixing of pollution with sea spray or dust particles over the sea surface. The lowest values of ω (0.84–0.70 between 370 and 950 nm) are measured in correspondence of a fresh plume possibly linked to ship emissions over the basin. The range of variability of ω observed in this study seems to be independent of the source region around the basin, as well as of the altitude and aging time of the plumes. The observed variability of ω reflects in a large variability for the complex refractive index of pollution aerosols, which is estimated to span in the large range 1.41–1.77 and 0.002–0.097 for the real and the imaginary parts, respectively, between 370 and 950 nm. Radiative calculations in clear-sky conditions were performed with the GAME radiative transfer model to test the sensitivity of the aerosol shortwave Direct Radiative Effect (DRE) to the variability of ω as observed in this study. Results from the calculations suggest up to a 50 and 30 % change of the forcing efficiency (FE), i.e. the DRE per unit of optical depth, at the surface (−160/−235 W m−2 τ−1 at 60° solar zenith angle) and at the Top-Of-Atmosphere (−137/−92 W m−2 τ−1) for ω varying between its maximum and minimum value. This induces a change of up to an order of magnitude (+23/+143 W m−2 τ−1) for the radiative effect within the atmosphere.

Shortwave direct radiative effects of above-cloud aerosols over global oceans derived from 8 years of CALIOP and MODIS observations

Abstract. In this paper, we studied the frequency of occurrence and shortwave direct radiative effects (DREs) of above-cloud aerosols (ACAs) over global oceans using 8 years (2007–2014) of collocated CALIOP and MODIS observations. Similar to previous work, we found high ACA occurrence in four regions: southeastern (SE) Atlantic region, where ACAs are mostly light-absorbing aerosols, i.e., smoke and polluted dust according to CALIOP classification, originating from biomass burning over the African Savanna; tropical northeastern (TNE) Atlantic and the Arabian Sea, where ACAs are predominantly windblown dust from the Sahara and Arabian deserts, respectively; and the northwestern (NW) Pacific, where ACAs are mostly transported smoke and polluted dusts from Asian. From radiative transfer simulations based on CALIOP–MODIS observations and a set of the preselected aerosol optical models, we found the DREs of ACAs at the top of atmosphere (TOA) to be positive (i.e., warming) in the SE Atlantic and NW Pacific regions, but negative (i.e., cooling) in the TNE Atlantic Ocean and the Arabian Sea. The cancellation of positive and negative regional DREs results in a global ocean annual mean diurnally averaged cloudy-sky DRE of 0.015 W m−2 (range of −0.03 to 0.06 W m−2) at TOA. The DREs at surface and within the atmosphere are −0.15 W m−2 (range of −0.09 to −0.21 W m−2), and 0.17 W m−2 (range of 0.11 to 0.24 W m−2), respectively. The regional and seasonal mean DREs are much stronger. For example, in the SE Atlantic region, the JJA (July–August) seasonal mean cloudy-sky DRE is about 0.7 W m−2 (range of 0.2 to 1.2 W m−2) at TOA. All our DRE computations are publicly available1. The uncertainty in our DRE computations is mainly caused by the uncertainties in the aerosol optical properties, in particular aerosol absorption, the uncertainties in the CALIOP operational aerosol optical thickness retrieval, and the ignorance of cloud and potential aerosol diurnal cycle. In situ and remotely sensed measurements of ACA from future field campaigns and satellite missions and improved lidar retrieval algorithm, in particular vertical feature masking, would help reduce the uncertainty. 1 https://drive.google.com/folderview?id=0B6gKx4dgNY0GMVYzcEd0bkZmRmc&usp=sharing

Absorption of aerosols above clouds from POLDER/PARASOL measurements and estimation of their direct radiative effect

Abstract. This study presents an original method to evaluate key parameters for the estimation of the direct radiative effect (DRE) of aerosol above clouds: the absorption of the the cloud albedo. It is based on multi-angle total and polarized radiances both provided by the A-train satellite instrument POLDER – Polarization and Directionality of Earth Reflectances. The sensitivities brought by each kind of measurements are used in a complementary way. Polarization mostly translates scattering processes and is thus used to estimate scattering aerosol optical thickness and aerosol size. On the other hand, total radiances, together with the scattering properties of aerosols, are used to evaluate the absorption optical thickness of aerosols and cloud optical thickness. The retrieval of aerosol and clouds properties (i.e., aerosol and cloud optical thickness, aerosol single scattering albedo and Ångström exponent) is restricted to homogeneous and optically thick clouds (cloud optical thickness larger than 3). In addition, a procedure has been developed to process the shortwave DRE of aerosols above clouds. Three case studies have been selected: a case of absorbing biomass burning aerosols above clouds over the southeast Atlantic Ocean, a Siberian biomass burning event and a layer of Saharan dust above clouds off the northwest coast of Africa. Besides these case studies, both algorithms have been applied to the southeast Atlantic Ocean and the results have been averaged during August 2006. The mean DRE is found to be 33.5 W m−2 (warming). Finally, the effect of the heterogeneity of clouds has been investigated and reveals that it affects mostly the retrieval of the cloud optical thickness and not greatly the aerosols properties. The homogenous cloud assumption used in both the properties retrieval and the DRE processing leads to a slight underestimation of the DRE.

Transport of anthropogenic and biomass burning aerosols from Europe to the Arctic during spring 2008

Abstract. During the POLARCAT-France airborne campaign in April 2008, pollution originating from anthropogenic and biomass burning emissions was measured in the European Arctic. We compare these aircraft measurements with simulations using the WRF-Chem model to investigate model representation of aerosols transported from Europe to the Arctic. Modeled PM2.5 is evaluated using European Monitoring and Evaluation Programme (EMEP) measurements in source regions and POLARCAT aircraft measurements in the Scandinavian Arctic. Total PM2.5 agrees well with the measurements, although the model overestimates nitrate and underestimates organic carbon in source regions. Using WRF-Chem in combination with the Lagrangian model FLEXPART-WRF, we find that during the campaign the research aircraft sampled two different types of European plumes: mixed anthropogenic and fire plumes from eastern Europe and Russia transported below 2 km, and anthropogenic plumes from central Europe uplifted by warm conveyor belt circulations to 5–6 km. Both modeled plume types had undergone significant wet scavenging (> 50% PM10) during transport. Modeled aerosol vertical distributions and optical properties below the aircraft are evaluated in the Arctic using airborne lidar measurements. Model results show that the pollution event transported aerosols into the Arctic (> 66.6° N) for a 4-day period. During this 4-day period, biomass burning emissions have the strongest influence on concentrations between 2.5 and 3 km altitudes, while European anthropogenic emissions influence aerosols at both lower (~ 1.5 km) and higher altitudes (~ 4.5 km). As a proportion of PM2.5, modeled black carbon and SO4= concentrations are more enhanced near the surface in anthropogenic plumes. The European plumes sampled during the POLARCAT-France campaign were transported over the region of springtime snow cover in northern Scandinavia, where they had a significant local atmospheric warming effect. We find that, during this transport event, the average modeled top-of-atmosphere (TOA) shortwave direct and semi-direct radiative effect (DSRE) north of 60° N over snow and ice-covered surfaces reaches +0.58 W m−2, peaking at +3.3 W m−2 at noon over Scandinavia and Finland.

Impact of four‐stream radiative transfer algorithm on aerosol direct radiative effect and forcing

AbstractLarge uncertainties remain in the estimation of aerosol direct radiative effect (DRE) and forcing (DRF). In this work, using an aerosol‐climate model with two‐ and four‐stream radiation schemes, we show that the radiative transfer algorithms contribute to the uncertainties. Aerosol shortwave DREs and heating rate are underestimated significantly by the two‐stream algorithm. For present‐day conditions, the four‐stream algorithms are found to enhance global annual mean aerosol shortwave DREs by more than 8% (14%) at the top of the atmosphere (TOA), 15% (18%) in the atmosphere, and 12% (15%) at the surface for all‐sky (clear‐sky) case. The regional‐averaged relative differences in aerosol shortwave DREs between the two‐ and four‐stream algorithms increase as latitude increases, exceeding 25% at the TOA and 30% at the surface in the high latitudes of the Southern Hemisphere. The DRE differences due to the four‐stream algorithms are negative, except for the Arctic, Tibetan Plateau, Arabia, and Sahara, at the TOA, are positive in the atmosphere, and are negative at the surface, with the maximum exceeding 4.0 W m−2. Increases in aerosol shortwave heating rates due to the four‐stream algorithms are generally more than 10% and may even exceed 100%. Our results also show that the two‐stream algorithm underestimates the DRFs due to anthropogenic aerosols. Significant underestimation appears in the middle latitudes of the Northern Hemisphere, with the maximum being close to the quantity of 0.6 W m−2 for clear‐sky case. This study indicates that a multi‐stream radiative transfer algorithm is necessary to reduce the uncertainties of aerosol DREs and DRFs estimated by global climate models.

A novel method for estimating shortwave direct radiative effect of above-cloud aerosols using CALIOP and MODIS data

Abstract. This paper describes an efficient and unique method for computing the shortwave direct radiative effect (DRE) of aerosol residing above low-level liquid-phase clouds using CALIOP (Cloud-Aerosol Lidar with Orthogonal Polarization) and MODIS (Moderate Resolution Imaging Spectroradiometer) data. It addresses the overlap of aerosol and cloud rigorously by utilizing the joint histogram of cloud optical depth and cloud top pressure while also accounting for subgrid-scale variations of aerosols. The method is computationally efficient because of its use of grid-level cloud and aerosol statistics, instead of pixel-level products, and a precomputed look-up table based on radiative transfer calculations. We verify that for smoke and polluted dust over the southeastern Atlantic Ocean the method yields a seasonal mean instantaneous (approximately 13:30 local time) shortwave DRE of above-cloud aerosol (ACA) that generally agrees with a more rigorous pixel-level computation within 4%. We also estimate the impact of potential CALIOP aerosol optical depth (AOD) retrieval bias of ACA on DRE. We find that the regional and seasonal mean instantaneous DRE of ACA over southeastern Atlantic Ocean would increase, from the original value of 6.4 W m−2 based on operational CALIOP AOD to 9.6 W m−2 if CALIOP AOD retrievals are biased low by a factor of 1.5 (Meyer et al., 2013) and further to 30.9 W m−2 if CALIOP AOD retrievals are biased low by a factor of 5 as suggested in Jethva et al. (2014). In contrast, the instantaneous ACA radiative forcing efficiency (RFE) remains relatively invariant in all cases at about 53 W m−2 AOD−1, suggesting a near-linear relation between the instantaneous RFE and AOD. We also compute the annual mean instantaneous shortwave DRE of light-absorbing aerosols (i.e., smoke and polluted dust) over global oceans based on 4 years of CALIOP and MODIS data. We find that given an above-cloud aerosol type the optical depth of the underlying clouds plays a larger role than above-cloud AOD in the variability of the annual mean shortwave DRE of above-cloud light-absorbing aerosol. While we demonstrate our method using CALIOP and MODIS data, it can also be extended to other satellite data sets.

Simultaneous retrieval of aerosol properties and clear-sky direct radiative effect over the global ocean from MODIS

A unified satellite algorithm is presented to simultaneously retrieve aerosol properties (aerosol optical depth; AOD and aerosol type) and clear-sky shortwave direct radiative effect (hereafter, DREA) over ocean. The algorithm is applied to Moderate Resolution Imaging spectroradiometer (MODIS) observations for a period from 2003 to 2010 to assess the DREA over the global ocean. The simultaneous retrieval utilizes lookup table (LUT) containing both spectral reflectances and solar irradiances calculated using a single radiative transfer model with the same aerosol input data. This study finds that aerosols cool the top-of-atmosphere (TOA) and bottom-of-atmosphere (BOA) by 5.2 ± 0.5 W/m2 and 8.3 W/m2, respectively, and correspondingly warm the atmosphere (hereafter, ATM) by 3.1 W/m2. These quantities, solely based on the MODIS observations, are consistent with those of previous studies incorporating chemical transport model simulations and satellite observations. However, the DREAs at BOA and ATM are expected to be less accurate compared to that of TOA due to low sensitivity in retrieving aerosol type information, which is related with the atmospheric heating by aerosols, particularly in low AOD conditions; consequently, the uncertainties could not be quantified. Despite the issue in the aerosol type information, the present method allows us to confine the DREA attributed only to fine-mode dominant aerosols, which are expected to be mostly anthropogenic origin, in the range from −1.1 W/m2 to −1.3 W/m2 at TOA. Improvements in size-resolved AOD and SSA retrievals from current and upcoming satellite instruments are suggested to better assess the DREA, particularly at BOA and ATM, where aerosol absorptivity induces substantial uncertainty.

Mineral dust aerosol net direct radiative effect during GERBILS field campaign period derived from SEVIRI and GERB

Colocated Spinning Enhanced Visible and Infrared Imager (SEVIRI) retrieved dust optical depths at 0.55 microns, τ055, and Geostationary Earth Radiation Budget (GERB) fluxes at the top of atmosphere are used to provide, for the first time, an observationally based estimate of the cloud‐free net direct radiative effect (DRE) of mineral dust aerosol from geostationary satellite observations, providing new insights into the influence of time of day on the magnitude and sign of the shortwave, longwave, and overall net effect during sunlit hours. Focusing on the Geostationary Earth Radiation Budget Intercomparison of Longwave and Shortwave radiation (GERBILS) campaign over North Africa during June 2007, the presence of mineral dust aerosol reduces the outgoing longwave radiation at all times of day with the peak reduction clearly following the diurnal cycle of surface temperature. The instantaneous shortwave DRE shows strong dependencies on pristine sky albedo and solar zenith angle such that the same dust loading can induce a positive or negative value dependent on time of day. However, the area mean net DRE over the GERBILS period is dominated by the longwave component at all sampled times of day, with mineral dust inducing a reduction in outgoing net flux of the order of 10W m−2. Hence, in the mean sense, Saharan dust is found to warm the Earth‐atmosphere system over northern Africa and the Middle East.

Aerosol shortwave direct radiative effect and forcing based on MODIS Level 2 data in the Eastern Mediterranean (Crete)

Abstract. The shortwave (SW) radiation budget was computed on a 10 km × 10 km resolution above FORTH-CRETE AERONET station in Crete, Greece, for the 11-year period from 2000 to 2010. The area is representative of the Eastern Mediterranean region, where air pollution and diminishing water resources are exacerbated by high aerosol loads and climate change. The present study aims to quantify the aerosol direct effect and forcing on the local surface and atmospheric energy budget. A radiative transfer model was used, with climatological data from the Moderate Resolution Imaging Spectroradiometer (MODIS), on board NASA's Terra and Aqua satellites. The instantaneous radiative fluxes were computed for satellite overpass times at the surface, within the atmosphere and at the top of atmosphere (TOA). Downward surface fluxes and aerosol input data were validated against ground measurements. Output fluxes reveal the direct radiative effects of dust events, with instantaneous values reaching up to −215, 139 and −46 Wm−2 at the surface (cooling), within the atmosphere (warming) and at TOA (cooling), respectively. Mean monthly values show a decreasing trend of the aerosol direct radiative effect, in agreement with a similar trend in AOT. The analysis of the contribution of anthropogenic and natural aerosol show major peaks of natural aerosol direct effect occurring mainly in spring, while a summer maximum is attributed to anthropogenic aerosol. During their peaks, anthropogenic aerosol forcing can reach values of −24 Wm−2 at the surface, 19 Wm−2 in the atmosphere and over −4 Wm−2 at TOA (monthly mean instantaneous values). The corresponding monthly peak values for natural aerosol are over −20 Wm−2, 12 Wm−2 and −9 Wm−2.