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From a passive satellite remote sensing point of view, the richest set of information on aerosol properties can be obtained from instruments that measure both intensity and polarization of backscattered sunlight at multiple wavelengths and multiple viewing angles for one ground pixel. However, it is challenging to exploit this information at a global scale because complex algorithms are needed with many fit parameters (aerosol and land/ocean reflection), based on online radiative transfer models. So far, two such algorithms have demonstrated this capability at a global scale: the Generalized Retrieval of Atmosphere and Surface Properties (GRASP) algorithm and the Remote sensing of Trace gas and Aerosol Products (RemoTAP) algorithm. In this paper, we present a detailed comparison of the most recent versions of RemoTAP and GRASP. We evaluate both algorithms for synthetic observations, for real PARASOL (Polarization and Anisotropy of Reflectances for Atmospheric Science coupled with Observations from a Lidar) observations against AERONET (Aerosol Robotic Network) for common pixels, and for global PARASOL retrievals for the year 2008. For the aerosol optical depth (AOD) over land, both algorithms show a root mean square error (RMSE) of 0.10 (at 550 nm). For single scattering albedo (SSA), both algorithms show a good performance in terms of RMSE (0.04), but RemoTAP has a smaller bias (0.002) compared to GRASP (0.021). For the Ångström exponent (AE), GRASP has a smaller RMSE (0.367) than RemoTAP (0.387), mainly caused by a small overestimate of AE at low values (large particles). Over ocean both algorithms perform very well. For AOD, RemoTAP has an RMSE of 0.057 and GRASP an even smaller RMSE of 0.047. For AE, the RMSEs of RemoTAP and GRASP are 0.285 and 0.224, respectively. Based on the AERONET comparison, we conclude that both algorithms show very similar overall performance, where both algorithms have stronger and weaker points. For the global data products, we find a root mean square difference (RMSD) between RemoTAP and GRASP AOD of 0.12 and 0.038 over land and ocean, respectively. The largest differences occur over the biomass burning region in equatorial Africa. The global mean values are virtually unbiased with respect to each other. For AE the RMSD between RemoTAP and GRASP is 0.33 over land and 0.23 over ocean. For SSA, we find much better agreement over land (bias = - 0.01, RMSD = 0.043 for retrievals with AOD > 0.2) than over ocean (bias = 0.053, RMSD = 0.074). As expected, the differences increase towards low AOD, over both land and ocean. We also compared the GRASP and RemoTAP AOD and AE products against MODIS. For AOD over land, the agreement of either GRASP or RemoTAP with MODIS is worse than the agreement between the two PARASOL algorithms themselves. Over ocean, the agreement is very similar among the three products for AOD. For AE, the agreement between GRASP and RemoTAP is much better than the agreement of both products with MODIS. The agreement of the latest product versions with each other and with AERONET improved significantly compared to the previous version of the global products of GRASP and RemoTAP. The results demonstrate that the dedicated effort in algorithm development for multi-angle polarimetric (MAP) aerosol retrievals still leads to substantial improvement of the resulting aerosol products, and this is still an ongoing process. [ABSTRACT FROM AUTHOR]

The Directional Polarization Camera (DPC) onboard the Chinese Gaofen-5 satellite, launched in May 2018, has similar specifications as the POLDER-3 instrument. The SRON Remote Sensing of Trace gas and Aerosol Products (RemoTAP) full retrieval algorithm is applied to DPC measurements to retrieve aerosol properties including the total Aerosol Optical Depth (AOD), the fine/coarse mode AOD and the SSA (Single Scattering Albedo). Measurements of the global ground-based AERONET network between December 2019 and April 2020 have been used for the validation of the DPC retrievals. According to the average Fine Mode Fraction (FMF) of the selected AERONET stations, the stations are divided into urban stations (FMF ≥ 0.5) and dust stations (FMF < 0.5). For the total AOD validation, DPC retrievals show better performance over urban stations than over dust stations, with average biases of 0.055 and 0.106, and RMSEs of 0.151 and 0.228, respectively. Regarding the fine mode AOD, the retrieval also performs better over urban stations. Compared with the total AOD validation, both the relatively lower bias (0.021 and 0.065) and the higher Gfrac (Fraction of Good retrieval, 63.8% and 47.3%, respectively) further indicate that DPC performs better when fine mode aerosols dominate. For the land SSA validation, most of our SSA retrievals (~71%) show differences with AERONET SSA retrievals lower than 0.05. Case studies over fire spots and dust over northern China demonstrate the encouraging application potential of DPC aerosol products. The difference between fine and coarse AOD can provide more aerosol source information compared with the total AOD alone. Since the SSA retrievals are particularly sensitive to absorbing fine particles, they can be easily used in the tracking of biomass burning aerosol. [ABSTRACT FROM AUTHOR]

Atmospheric aerosols have been known to be a major source of uncertainties in CO2 concentrations retrieved from space. In this study, we investigate the added value of multi-angle polarimeter (MAP) measurements in the context of the Copernicus candidate mission for anthropogenic CO2 monitoring (CO2M). To this end, we compare aerosol-induced XCO2 errors from standard retrievals using spectrometer only (without MAP) with those from retrievals using both MAP and spectrometer. MAP observations are expected to provide information about aerosols that is useful for improving XCO2 accuracy. For the purpose of this work, we generate synthetic measurements for different atmospheric and geophysical scenes over land, based on which XCO2 retrieval errors are assessed. We show that the standard XCO2 retrieval approach that makes no use of auxiliary aerosol observations returns XCO2 errors with an overall bias of 1.12 ppm, and a spread (defined as half of the 15.9th to the 84.1th percentile range) of 2.07 ppm. The latter is far higher than the required XCO2 accuracy (0.5 ppm) and precision (0.7 ppm) of the CO2M mission. Moreover, these XCO2 errors exhibit a significantly larger bias and scatter at high aerosol optical depth, high aerosol altitude, and low solar zenith angle, which could lead to a worse performance in retrieving XCO2 from polluted areas where CO2 and aerosols are co-emitted. We proceed to determine MAP instrument specifications in terms of wavelength range, number of viewing angles, and measurement uncertainties that are required to achieve XCO2 accuracy and precision targets of the mission. Two different MAP instrument concepts are considered in this analysis. We find that for either concept, MAP measurement uncertainties on radiance and degree of linear polarization should be no more than 3 % and 0.003, respectively. Adopting the derived MAP requirements, a retrieval exercise using both MAP and spectrometer measurements of the synthetic scenes delivers XCO2 errors with an overall bias of −0.004 ppm and a spread of 0.54 ppm, implying compliance with the CO2M mission requirements; the very low bias is especially important for proper emission estimates. For the test ensemble, we find effectively no dependence of the XCO2 errors on aerosol optical depth, altitude of the aerosol layer, and solar zenith angle. These results indicate a major improvement in the retrieved XCO2 accuracy with respect to the standard retrieval approach, which could lead to a higher data yield, better global coverage, and a more comprehensive determination of CO2 sinks and sources. As such, this outcome underlines the contribution of, and therefore the need for, a MAP instrument onboard the CO2M mission. [ABSTRACT FROM AUTHOR]

For aerosol retrieval from multi-angle polarimetric (MAP) measurements over the ocean it is important to accurately account for the contribution of the ocean-body to the top-of-atmosphere signal, especially for wavelengths <500 nm. Performing online radiative transfer calculations in the coupled atmosphere ocean system is too time consuming for operational retrieval algorithms. Therefore, mostly lookup-tables of the ocean body reflection matrix are used to represent the lower boundary in an atmospheric radiative transfer model. For hyperspectral measurements such as those from Spectro-Polarimeter for Planetary Exploration (SPEXone) on the NASA Plankton, Aerosol, Cloud and ocean Ecosystem (PACE) mission, also the use of look-up tables is unfeasible because they will become too big. In this paper, we propose a new method for aerosol retrieval over ocean from MAP measurements using a neural network (NN) to model the ocean body reflection matrix. We apply the NN approach to synthetic SPEXone measurements and also to real data collected by SPEX airborne during the Aerosol Characterization from Polarimeter and Lidar (ACEPOL) campaign. We conclude that the NN approach is well capable for aerosol retrievals over ocean, introducing no significant error on the retrieved aerosol properties [ABSTRACT FROM AUTHOR]

• PCF suite is the first dedicated satellite sensor for PM 2.5 remote sensing. • The principle of PCF composed by DPC and POSP are described. • Retrievals of aerosols and PM 2.5 by PMRS model are investigated. • The errors propagation from aerosols to PM 2.5 retrievals are discussed. Focusing on satellite remote sensing of fine particulate matter PM 2.5 from space, the polarization crossfire (PCF) strategy has been developed, which includes the PCF satellite suite and the particulate matter remote sensing (PMRS) model. Expected to be the first dedicated satellite sensor for PM 2.5 remote sensing globally, the PCF suite is composed by the Particulate Observing Scanning Polarimeter (POSP) and the Directional Polarimetric Camera (DPC) together, and will be launched on board the Chinese GaoFen-5(02) satellite in 2021. Since the cross-track polarimetric measurements of POSP fully cover the multi-viewing swath of DPC, the sophisticated joint measurements could be obtained from the PCF suite in the range of 380–2250 nm including intensity and polarization, by the means of pixel matching and the cross calibration from POSP to DPC. Based on the optimal estimation inversion framework and synthetic data of PCF, the retrieval performances of key aerosol parameters are systematically investigated and assessed for the PM 2.5 estimation by the PMRS model. For the design of inversion strategy for PCF, we firstly test the retrievals of aerosol optical depth (AOD), fine mode fraction (FMF), aerosol layer height (H) and the fine-mode real part of complex refractive index (m r f) simultaneously with surface parameters from the synthetic PCF data, and then the columnar volume-to-extinction ratio of fine particulates (VE f), the aerosol effective density (ρ f) and the hygroscopic growth factor of fine-mode particles (f (RH)) are further obtained by the corresponding empirical relationship. The propagation errors from aerosol parameters to PM 2.5 retrieval are investigated with the key procedures of PMRS model. In addition, the influences of improving calibration accuracy of PCF on PM 2.5 retrievals are discussed, as well as the retrieval feasibility of PM 10 by PCF strategy. [ABSTRACT FROM AUTHOR]