Abstract. Instruments dedicated to aerosol monitoring are recently available and the POLDER (POLarization and Directionality of the Earth's Reflectances) instrument on board the PARASOL (Polarization & Anisotropy of Reflectances for Atmospheric Sciences coupled with Observations from a Lidar) mission is one of them. By measuring the spectral, angular and polarization properties of the radiance at the top of the atmosphere, in coordination with the other A-Train instruments, PARASOL provides the aerosol optical depths (AOD) as well as several optical and microphysical aerosol properties. The instrument, the inversion schemes and the list of aerosol parameters are described. Examples of retrieved aerosol parameters are provided as well as innovative approaches and further inversion techniques.
[1] We present a new approach to retrieve the aerosol properties over land that uses accurate polarization measurements over a broad spectral (410-2250 nm) and angular (±60°from nadir) ranges. The approach uses longer wavelength observations to accurately estimate the surface effects, and it is incorporated into an optimal estimation framework for retrieving the particle number density and a detailed aerosol microphysical model: effective radius, variance, and complex refractive index. A sensitivity analysis shows that the uncertainties in aerosol optical thickness (AOT) increase with AOT while the uncertainties in the microphysical model decrease. The uncertainty in the single scattering albedo (SSA) is notably less than 0.05 by the time the AOT is greater than 0.2. We find that calibration is the major source of uncertainty and that perfect angular and spectral correlation of calibration errors reduces the uncertainties in retrieved quantities. Finally, we observe that shorter wavelength (<500 nm) observations are crucial for determining the aerosols vertical extent and imaginary refractive index from polarization measurements. The retrieval approach is tested under pristine and polluted conditions using observations made by the Research Scanning Polarimeter during the Aerosol Lidar Validation experiment and over California Southern wild fires. In both cases we find that the retrievals are within the combined uncertainties of the retrieval and the Aerosol Robotic Network Cimel products and Total Ozone Mapping Spectrometer Aerosol Index. This demonstrates the unique capability of polarization measurements to accurately retrieve AOTs under pristine conditions and provide estimation of the SSA at higher AOTs.
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.
The detection of aerosol above clouds is critical for the estimate of both the aerosol and cloud radiative impacts. In this study, the authors present a new method to retrieve the aerosol properties over clouds that uses the multiangle polarization measurements of the Polarization and Directionality of Earth Reflectances (POLDER)–Polarization and Anisotropy of Reflectances for Atmospheric Sciences Coupled with Observations from a Lidar (PARASOL) instrument. The method is illustrated and applied to a case study exploiting the coincident observations from other passive and active sensors of the NASA A-Train satellite constellation. The case study is relative to an elevated biomass burning aerosol layer that originates from southern Africa and is then transported over low-level clouds extending over the Atlantic Ocean. It is shown that the comparison between the cloud-top heights retrieved with the different passive techniques developed for the A-Train sensors can be used to detect the presence of aerosols above clouds. The analysis of the PARASOL observations showed that the aerosols significantly affect the polarized light reflected by the clouds over the 80°–120° scattering angle range and in the rainbow region. A single scattering model permitted the reproduction of the polarization observations and the retrieval of an estimate of the aerosol layer optical thickness of 0.225 at 0.865 μm. The retrieved aerosol optical thicknesses over clouds agree quantitatively with the closest ones retrieved over clear-sky ocean (±0.04 as a maximum departure), demonstrating the value of the method. This innovative technique based solely on passive measurements is expected to provide a better understanding of aerosol properties in regions where significant cloud cover usually prevents the retrieval of aerosol optical thickness. As such, this new retrieval method can provide significant and valuable information about the radiative impact of clouds and aerosols, especially where they can potentially interact strongly with each other.
The Aerosol, Radiation and Clouds in southern Africa (AEROCLO-sA) project investigates the role of aerosols on the regional climate of southern Africa. This is a unique environment where natural and anthropogenic aerosols and a semipermanent and widespread stratocumulus (Sc) cloud deck are found. The project aims to understand the dynamical, chemical, and radiative processes involved in aerosol–cloud–radiation interactions over land and ocean and under various meteorological conditions. The AEROCLO-sA field campaign was conducted in August and September of 2017 over Namibia. An aircraft equipped with active and passive remote sensors and aerosol in situ probes performed a total of 30 research flight hours. In parallel, a ground-based mobile station with state-of-the-art in situ aerosol probes and remote sensing instrumentation was implemented over coastal Namibia, and complemented by ground-based and balloonborne observations of the dynamical, thermodynamical, and physical properties of the lower troposphere. The focus laid on mineral dust emitted from salty pans and ephemeral riverbeds in northern Namibia, the advection of biomass-burning aerosol plumes from Angola subsequently transported over the Atlantic Ocean, and aerosols in the marine boundary layer at the ocean–atmosphere interface. This article presents an overview of the AEROCLO-sA field campaign with results from the airborne and surface measurements. These observations provide new knowledge of the interactions of aerosols and radiation in cloudy and clear skies in connection with the atmospheric dynamics over southern Africa. They will foster new advanced climate simulations and enhance the capability of spaceborne sensors, ultimately allowing a better prediction of future climate and weather in southern Africa.
Abstract. The Chemistry-Aerosol Mediterranean Experiment (ChArMEx; http://charmex.lsce.ipsl.fr) is a collaborative research program federating international activities to investigate Mediterranean regional chemistry-climate interactions. A special observing period (SOP-1a) including intensive airborne measurements was performed in the framework of the Aerosol Direct Radiative Impact on the regional climate in the MEDiterranean region (ADRIMED) project during the Mediterranean dry season over the western and central Mediterranean basins, with a focus on aerosol-radiation measurements and their modeling. The SOP-1a took place from 11 June to 5 July 2013. Airborne measurements were made by both the ATR-42 and F-20 French research aircraft operated from Sardinia (Italy) and instrumented for in situ and remote-sensing measurements, respectively, and by sounding and drifting balloons, launched in Minorca. The experimental setup also involved several ground-based measurement sites on islands including two ground-based reference stations in Corsica and Lampedusa and secondary monitoring sites in Minorca and Sicily. Additional measurements including lidar profiling were also performed on alert during aircraft operations at EARLINET/ACTRIS stations at Granada and Barcelona in Spain, and in southern Italy. Remote-sensing aerosol products from satellites (MSG/SEVIRI, MODIS) and from the AERONET/PHOTONS network were also used. Dedicated meso-scale and regional modeling experiments were performed in relation to this observational effort. We provide here an overview of the different surface and aircraft observations deployed during the ChArMEx/ADRIMED period and of associated modeling studies together with an analysis of the synoptic conditions that determined the aerosol emission and transport. Meteorological conditions observed during this campaign (moderate temperatures and southern flows) were not favorable to producing high levels of atmospheric pollutants or intense biomass burning events in the region. However, numerous mineral dust plumes were observed during the campaign, with the main sources located in Morocco, Algeria and Tunisia, leading to aerosol optical depth (AOD) values ranging between 0.2 and 0.6 (at 440 nm) over the western and central Mediterranean basins. One important point of this experiment concerns the direct observations of aerosol extinction onboard the ATR-42, using the CAPS system, showing local maxima reaching up to 150 M m −1 within the dust plume. Non-negligible aerosol extinction (about 50 M m −1 ) has also been observed within the marine boundary layer (MBL). By combining the ATR-42 extinction coefficient observations with absorption and scattering measurements, we performed a complete optical closure revealing excellent agreement with estimated optical properties. This additional information on extinction properties has allowed calculation of the dust single scattering albedo (SSA) with a high level of confidence over the western Mediterranean. Our results show a moderate variability from 0....
Most of the current aerosol retrievals from passive sensors are restricted to cloud-free scenes, which strongly reduces our ability to monitor the aerosol properties at a global scale and to estimate their radiative forcing. The presence of aerosol above clouds (AAC) affects the polarized light reflected by the cloud layer, as shown by the spaceborne measurements provided by the POlarization and Directionality of Earth Reflectances (POLDER) instrument on the PARASOL satellite. In a previous work, a first retrieval method was developed for AAC scenes and evaluated for biomass-burning aerosols transported over stratocumulus clouds. The method was restricted to the use of observations acquired at forward scattering angles (90–120°) where polarized measurements are highly sensitive to fine-mode particle scattering. Non-spherical particles in the coarse mode, such as mineral dust particles, do not much polarize light and cannot be handled with this method. In this paper, we present new developments that allow retrieving also the properties of mineral dust particles above clouds. These particles do not much polarize light but strongly reduce the polarized cloud bow generated by the liquid cloud layer beneath and observed for scattering angles around 140°. The spectral attenuation can be used to qualitatively identify the nature of the particles (i.e. accumulation mode versus coarse mode, i.e. mineral dust particles versus biomass-burning aerosols), whereas the magnitude of the attenuation is related to the optical thickness of the aerosol layer. We also use the polarized measurements acquired in the cloud bow to improve the retrieval of both the biomass-burning aerosol properties and the cloud microphysical properties. We provide accurate polarized radiance calculations for AAC scenes and evaluate the contribution of the POLDER polarization measurements for the simultaneous retrieval of the aerosol and cloud properties. We investigate various scenes with mineral dust particles and biomass-burning aerosols above clouds. For clouds, our results confirm that the droplet size distribution is narrow in high-latitude ocean regions and that the droplet effective radii retrieved from both polarization measurements and from total radiance measurements are generally close for AAC scenes (departures smaller than 2 μm). We found that the magnitude of the primary cloud bow cannot be accurately estimated with a plane parallel transfer radiative code. The errors for the modeling of the polarized cloud bow are between 4 and 8% for homogenous cloudy scenes, as shown by a 3-D radiative transfer code. These effects only weakly impact the retrieval of the Aerosol Optical Thickness (AOT) performed with a mineral dust particle model for which the microphysical properties are entirely known (relative error smaller than 6%). We show that the POLDER polarization measurements allow retrieving the AOT, the fine-mode particle size, the Ångström exponent and the fraction of spherical particles. However, the complex refractive index and the coarse-...
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