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Mineral dust significantly influences the Earth's climate system by affecting the radiative balance through the emission, absorption and scattering of solar and terrestrial radiation. Estimating the dust radiative effect remains challenging due to the lack of detailed information on the physical and chemical properties of dust. High-spectral-resolution instruments in the infrared (IR) spectrum, such as the Infrared Atmospheric Sounding Instrument (IASI), have demonstrated the ability to quantify these aerosol properties. A crucial parameter for characterizing mineral dust from space is the complex refractive index (CRI), as it links the dust's physical and chemical properties to its optical properties. This paper examines the impact of six prior laboratory CRI datasets to improve the characterization of dust microphysical properties using IASI. The CRIs include older measurements obtained through the classical pellet method, commonly employed in mineral dust applications, as well as newer datasets that incorporate the latest advancements in laboratory measurement techniques for aerosol generation. These datasets are tested on IASI measurements during a dust storm event over the Gobi Desert in May 2017. We evaluate the sensitivity of IASI to different CRI datasets using the Atmospheric Radiation Algorithm for High-Spectral Resolution Measurements from Infrared Spectrometer (ARAHMIS) radiative transfer algorithm and explore the datasets' impact on retrieving size distribution parameters by mapping their spatial distributions. The results indicate that the laboratory CRI datasets decrease the total error in the covariance matrix by 30 %. In addition, we assess the ability to accurately reconstruct IASI detections and the extent to which we can retrieve the microphysical properties of dust particles. The choice of CRI significantly impacts the accuracy of dust detection and characterization from satellite observations. Notably, datasets that incorporate recent aerosol generation techniques with higher spectral resolution and samples from the case study region show improved compatibility with IASI observations. The outcomes of this research emphasize two key points: the crucial link between chemical composition of dust and its optical properties and the importance of considering the specific composition of the CRI dataset for improved retrieval of the microphysical parameters. Furthermore, this study highlights the critical role of ongoing enhancements in CRI measurement approaches, as well as the potential of high-spectral-resolution infrared sounders for aerosol atmospheric investigation and for understanding the radiative impacts of sounders. [ABSTRACT FROM AUTHOR]

This study focuses on the characterization of aerosol hygroscopicity using remote sensing techniques. We employ a Mie–Raman–fluorescence lidar (Lille Lidar for Atmospheric Study, LILAS), developed at the ATOLL platform, Laboratoire d'Optique Atmosphérique, Lille, France, in combination with the RPG-HATPRO-G5 microwave radiometer to enable continuous aerosol and water vapor monitoring. We identify hygroscopic growth cases when an aerosol layer exhibits an increase in both aerosol backscattering coefficient and relative humidity. By examining the fluorescence backscattering coefficient, which remains unaffected by the presence of water vapor, the potential temperature, and the absolute humidity, we verify the homogeneity of the aerosol layer. Consequently, the change in the backscattering coefficient is solely attributed to water uptake. The Hänel theory is employed to describe the evolution of the backscattering coefficient with relative humidity and introduces a hygroscopic coefficient, γ , which depends on the aerosol type. The particularity of this method revolves around the use of the fluorescence which is employed to take into account and correct the aerosol concentration variations in the layer. Case studies conducted on 29 July and 9 March 2021 examine, respectively, an urban and a smoke aerosol layer. For the urban case, γ is estimated as 0.47 ± 0.03 at 532 nm; as for the smoke case, the estimation of γ is 0.5 ± 0.3. These values align with those reported in the literature for urban and smoke particles. Our findings highlight the efficiency of the Mie–Raman–fluorescence lidar and microwave radiometer synergy in characterizing aerosol hygroscopicity. The results contribute to advance our understanding of atmospheric processes, aerosol–cloud interactions, and climate modeling. [ABSTRACT FROM AUTHOR]

We present the capabilities of a compact dual-wavelength depolarization lidar to assess the spatiotemporal variations in aerosol properties aboard moving vectors. Our approach involves coupling the lightweight Cimel CE376 lidar, which provides measurements at 532 and 808 nm and depolarization at 532 nm , with a photometer to monitor aerosol properties. The assessments, both algorithmic and instrumental, were conducted at ATOLL (ATmospheric Observatory of LiLle) platform operated by the Laboratoire d'Optique Atmosphérique (LOA), in Lille, France. An early version of the CE376 lidar co-located with the CE318-T photometer and with a multi-wavelength Raman lidar were considered for comparisons and validation. We developed a modified Klett inversion method for simultaneous two-wavelength elastic lidar and photometer measurements. Using this setup, we characterized aerosols during two distinct events of Saharan dust and dust smoke aerosols transported over Lille in spring 2021 and summer 2022. For validation purposes, comparisons against the Raman lidar were performed, demonstrating good agreement in aerosol properties with relative differences of up to 12 % in the depolarization measurements. Moreover, a first dataset of CE376 lidar and photometer performing on-road measurements was obtained during the FIREX-AQ (Fire Influence on Regional to Global Environments and Air Quality) field campaign deployed in summer 2019 over the northwestern USA. By lidar and photometer mapping in 3D, we investigated the transport of released smoke from active fire spots at William Flats (northeast WA, USA). Despite extreme environmental conditions, our study enabled the investigation of aerosol optical properties near the fire source, distinguishing the influence of diffuse, convective, and residual smoke. Backscatter, extinction profiles, and column-integrated lidar ratios at 532 and 808 nm were derived for a quality-assured dataset. Additionally, the extinction Ångström exponent (EAE), color ratio (CR), attenuated color ratio (ACR), and particle linear depolarization ratio (PLDR) were derived. In this study, we discuss the capabilities (and limitations) of the CE376 lidar in bridging observational gaps in aerosol monitoring, providing valuable insights for future research in this field. [ABSTRACT FROM AUTHOR]

A mobile laboratory integrating lidar, sun photometer and in situ instruments has been deployed to observe the aerosol spatial variability in North China Plain in May 2017. Results from the campaign are presented.

The mobile system described in this paper integrates a commercial eye-safe lidar (CIMEL), a sunphotometer and in situ instruments. The system is distinguished by other transportable platforms through its capabilities to perform onroad measurements. The potential of a commercial lidar to provide reliable information on aerosol properties is investigated through comparison with a multi-wavelength Raman lidar. First results from observation campaigns in northern France are presented.

The study presents a climatology of aerosol composition concentration obtained by a recently developed GRASP/Component (GRASP stands for the Generalized Retrieval of Atmosphere and Surface Properties algorithm) approach applied to the whole archive of POLDER-3 observations. The conceptual specific of the GRASP/Component approach is in direct retrieval of aerosol speciation (component fraction) without an intermediate retrievals of aerosol optical characteristics. Despite a global validation of the derived aerosol component product is challenging, the results obtained are in line with general knowledge about aerosol types in different regions. In addition, we compare the GRASP derived black carbon and dust components with those of the MERRA-2 (Modern-Era Retrospective Analysis for Research and Applications, version 2) product. Quite reasonable general agreement in spatial and temporal distribution of the species provided by GRASP and MERRA-2 was found, the differences however appeared in regions known for strong biomass burning and dust emissions; the reasons for the discrepancies are discussed. The other derived components, such as concentration of absorbing (black carbon, brown carbon, iron oxides content in mineral dust) and scattering (ammonium sulphate and nitrate, organic carbon, non-absorbing dust) aerosol, represent scarce but imperative information for validation and potential adjustment of chemical transport models. The aerosol optical properties derived by GRASP/Component were found to agree well with the AERONET ground reference data and fully consistent with the previous GRASP Optimized, High Precision and Models retrieval versions applied to POLDER-3 data. Thus, the presented extensive climatology product provides an opportunity for understanding variabilities and trends in global and regional distributions of aerosol species. The climatology of the aerosol components obtained in addition to the aerosol optical properties provides additional valuable, qualitatively new inside about aerosol distributions and, therefore, demonstrates advantages of multi-angular polarimetric satellite observations as the next frontier for aerosol inversion from advanced satellite observations. [ABSTRACT FROM AUTHOR]

Proven by multiple theoretical and practical studies, multi-angular spectral polarimetry is ideal for comprehensive retrieval of properties of aerosols. Furthermore, a large number of advanced space polarimeters have been launched recently or planned to be deployed in the coming few years (Dubovik et al., 2019). Nevertheless, at present, practical utilization of aerosol products from polarimetry is rather limited, due to the relatively small amount of polarimetric observations compared to photometric observations, as well as challenges in making full use of the extensive information content available in these complex observations. Indeed, while in recent years several new algorithms have been developed to provide enhanced aerosol retrievals from satellite polarimetry, the practical value of available aerosol products from polarimeters yet remains to be proven. In this regard, this paper presents the analysis of aerosol products obtained by the Generalized Retrieval of Atmosphere and Surface Properties (GRASP) algorithm from POLDER/PARASOL observations. After about a decade of development, GRASP has been adapted for operational processing of polarimetric satellite observations and several aerosol products from POLDER/PARASOL observations have been released. These updated PARASOL/GRASP products are publicly available (e.g., http://www.icare.univ-lille.fr, www.grasp-open.com/products/), the dataset used in the current study is registered under: https://doi.org/10.5281/zenodo.3887265 (Chen et al., 2020). The objective of this study is to comprehensively evaluate the GRASP aerosol products obtained from POLDER/PARASOL observations. First, the validation of the entire 2005-2013 archive was conducted by comparing to ground-based Aerosol Robotic Network (AERONET) data. The subjects of the validation are spectral aerosol optical depth (AOD), aerosol absorption optical depth (AAOD) and single scattering albedo (SSA) at 6 wavelengths, as well as Ångström exponent (AE), fine mode AOD (AODF) and coarse mode AOD (AODC) interpolated to the reference wavelength 550 nm. Second, an inter-comparison of PARASOL/GRASP products with the PARASOL/Operational, MODIS Dark Target (DT), Deep Blue (DB) and Multi Angle Implementation of Atmospheric Correction (MAIAC) aerosol products for the year 2008 was performed. Over land both satellite data validations and inter-comparisons were conducted separately for different surface types, discriminated by bins of Normalized Difference Vegetation Index (NDVI): < 0.2, 0.2 ≤ and < 0.4, 0.4 ≤ and < 0.6, and ≥ 0.6. Three PARASOL/GRASP products were analyzed: GRASP/HP (High Precision), Optimized, and Models. These different products are consistent but were obtained using different assumptions in aerosol modeling with different accuracies of atmospheric radiative transfer (RT) calculations. Specifically, when using GRASP/HP or Optimized there is direct retrieval of the aerosol size distribution and spectral complex index of refraction. When using GRASP/Models, the aerosol is approximated by a mixture of several aerosol components, each with their own fixed size distribution and optical properties, and only the concentrations of those components are retrieved. GRASP/HP employs the most accurate RT calculations, while GRASP/Optimized and GRASP/Models are optimized to achieve the best trade-off between accuracy and speed. In all these options, the underlying surface reflectance is retrieved simultaneously with the aerosol properties and the radiative transfer calculations are performed on line during the retrieval. All validation results obtained for the full archive of PARASOL/GRASP products show solid quality of retrieved aerosol characteristics. The GRASP/Models retrievals, however, provided the most solid AOD products, e.g. AOD (550 nm) is unbiased, has the highest correlation (R~0.92) and the highest fraction of retrievals (~55.3%) satisfying the accuracy requirements of the Global Climate Observing System (GCOS) when compared to AERONET observations. GRASP/HP and GRASP/Optimized AOD products show a non-negligible positive bias (~0.07) when AOD is low (< 0.2). On the other hand, the detailed aerosol microphysical characteristics (AE, AODF, AODC and SSA, etc.) provided by GRASP/HP and GRASP/Optimized correlate generally better with AERONET than do the results of GRASP/Models. Overall, GRASP/HP processing demonstrates the high quality of microphysical characteristics retrieval versus AERONET. Evidently, GRASP/Models approach is more adapted for retrieval of total AOD, while the detailed aerosol microphysical properties are limited when a mixture of aerosol models with fixed optical properties are used. The results of a comparative analysis of PARASOL/GRASP and MODIS products showed that, based on validation against AERONET, the PARASOL/GRASP AOD (550 nm) product is of similar and sometimes of higher quality compared to the MODIS products. All AOD retrievals are more accurate and in good agreement over ocean. Over land, especially over bright surfaces, the retrieval quality degrades and the differences in total AOD products increase. The detailed aerosol characteristics, such as AE, AODF and AODC from PARASOL/GRASP are generally more reliable, especially over land. The global inter-comparisons of PARASOL/GRASP versus MODIS showed rather robust agreement, though some patterns and tendencies were observed. Over ocean, PARASOL/Models and MODIS/DT AOD agree well with the correlation coefficient of 0.92. Over land, the correlation between PARASOL/Models and the different MODIS products is lower, ranging from 0.76 to 0.85. There is no significant global offset; though over bright surfaces MODIS products tend to show higher values compared to PARASOL/Models when AOD is low, and smaller values for moderate and high AODs. Seasonal means suggest that PARASOL/GRASP products show more biomass burning aerosol loading in central Africa and dust over the Taklamakan Desert, but less AOD in the northern Sahara. It is noticeable also that the correlation for the data over AERONET sites is somewhat higher, suggesting that the retrieval assumptions generally work better over AERONET sites than over the rest of the globe. One of the potential reasons may be that MODIS retrievals, in general, rely more on AERONET climatology than GRASP retrievals. Overall, the analysis shows that the quality of AOD retrieval from multi-angular polarimetric observations like POLDER is at least comparable to those of single-viewing MODIS-like imagers. At the same time, the multi-angular polarimetric observations provide more information on other aerosol properties (e.g. spectral AODF, AODC, AE), as well as additional parameters such as AAOD and SSA. [ABSTRACT FROM AUTHOR]

We invert global black carbon (BC), organic carbon (OC) and desert dust (DD) aerosol emissions from POLDER/PARASOL spectral aerosol optical depth (AOD) and aerosol absorption optical depth (AAOD) using the GEOS-Chem inverse modelling framework. Our inverse modeling framework uses standard a priori emissions to provide a posteriori emissions that are constrained by POLDER/PARASOL AODs and AAODs. The following global emission values were retrieved for the three aerosol components: 18.4 Tg/yr for BC, 109.9 Tg/yr for OC, and 731.6 Tg/yr for DD for the year 2010. These values show a difference of +166.7 %, +184.0 %, and -42.4 % with respect to the a priori values of emission inventories used in "standard" GEOS-Chem runs. The model simulations using a posteriori emissions (i.e. retrieved emissions) provide values of 0.119 for global mean AOD and 0.0071 for AAOD at 550 nm, which are +13.3 % and +82.1 % higher than the AOD and AAOD obtained using the a priori values of emissions. Additionally, the a posteriori model simulation of AOD, AAOD, single scattering albedo, Ångström exponent, and absorption Ångström exponent show better agreement with independent AERONET, MODIS, and OMI measurements than the a priori simulation. Thus, this study suggests that using satellite-constrained global aerosol emissions in aerosol transport models can improve the accuracy of simulated global aerosol properties. [ABSTRACT FROM AUTHOR]

This study presents a novel methodology for remote monitoring of aerosol composition over large spatial and temporal domains. The concept is realized within the GRASP (Generalized Retrieval of Aerosol and Surface Properties) algorithm to directly infer aerosol composition from the measured radiances. This approach is different from the conventional methods that use post-processing of the retrieved aerosol optical properties for aerosol typing. The proposed method assumes observed aerosols as mixtures of particles composed of black carbon, brown carbon, absorbing insoluble, non-absorbing insoluble embedded in a soluble host. The algorithm then derives size distribution and the fractions of these components. The complex refractive index of each component is fixed a priori and the complex refractive index of mixture is computed using mixing rules. The approach is first tested with synthetic data and the uncertainties are estimated. Then, it is applied to the real ground-based AERONET and space-borne POLDER/PARASOL observations, known to be sensitive to aerosol complex refractive index. The study presents a first attempt to derive aerosol composition from satellites. The obtained aerosol optical characteristics are highly consistent with the standard products (R of ~ 0.9 for aerosol optical thickness). The approach also presented an ability to separate between aerosol properties in fine and coarse size fractions, in case of POLDER/PARASOL and AERONET. Examples of application to POLDER/PARASOL on the global scale are presented. The obtained spatial and temporal patterns of the aerosol composition agree well with our knowledge on aerosol sources and transport features. Finally, limitations and perspectives are discussed. [ABSTRACT FROM AUTHOR]