Vertical assessment of the mineral dust optical and microphysical properties as retrieved from the synergy between polarized micro-pulse lidar and sun/sky photometer observations using GRASP code

2021 ◽  
pp. 105818
Author(s):  
María-Ángeles López-Cayuela ◽  
Marcos Herreras-Giralda ◽  
Carmen Córdoba-Jabonero ◽  
Anton Lopatin ◽  
Oleg Dubovik ◽  
...  
2021 ◽  
Author(s):  
María Ángeles López Cayuela ◽  
Carmen Córdoba-Jabonero ◽  
Daniel Pérez-Ramírez ◽  
Milagros Herrera ◽  
Juan Luís Guerrero-Rascado

2020 ◽  
Vol 12 (5) ◽  
pp. 785 ◽  
Author(s):  
Tong Wu ◽  
Zhanqing Li ◽  
Jun Chen ◽  
Yuying Wang ◽  
Hao Wu ◽  
...  

Water uptake by aerosol particles alters its light-scattering characteristics significantly. However, the hygroscopicities of different aerosol particles are not the same due to their different chemical and physical properties. Such differences are explored by making use of extensive measurements concerning aerosol optical and microphysical properties made during a field experiment from December 2018 to March 2019 in Beijing. The aerosol hygroscopic growth was captured by the aerosol optical characteristics obtained from micropulse lidar, aerosol chemical composition, and aerosol particle size distribution information from ground monitoring, together with conventional meteorological measurements. Aerosol hygroscopicity behaves rather distinctly for mineral dust coarse-mode aerosol (Case I) and non-dust fine-mode aerosol (Case II) in terms of the hygroscopic enhancement factor, f β ( R H , λ 532 ) , calculated for the same humidity range. The two types of aerosols were identified by applying the polarization lidar photometer networking method (POLIPHON). The hygroscopicity for non-dust aerosol was much higher than that for dust conditions with the f β ( R H , λ 532 ) being around 1.4 and 3.1, respectively, at the relative humidity of 86% for the two cases identified in this study. To study the effect of dust particles on the hygroscopicity of the overall atmospheric aerosol, the two types of aerosols were identified and separated by applying the polarization lidar photometer networking method in Case I. The hygroscopic enhancement factor of separated non-dust fine-mode particles in Case I had been significantly strengthened, getting closer to that of the total aerosol in Case II. These results were verified by the hygroscopicity parameter, κ (Case I non-dust particles: 0.357 ± 0.024; Case II total: 0.344 ± 0.026), based on the chemical components obtained by an aerosol chemical speciation instrument, both of which showed strong hygroscopicity. It was found that non-dust fine-mode aerosol contributes more during hygroscopic growth and that non-hygroscopic mineral dust aerosol may reduce the total hygroscopicity per unit volume in Beijing.


2018 ◽  
Vol 18 (3) ◽  
pp. 2119-2138 ◽  
Author(s):  
Xin Wang ◽  
Hui Wen ◽  
Jinsen Shi ◽  
Jianrong Bi ◽  
Zhongwei Huang ◽  
...  

Abstract. Mineral dust aerosols (MDs) not only influence the climate by scattering and absorbing solar radiation but also modify cloud properties and change the ecosystem. From 3 April to 16 May 2014, a ground-based mobile laboratory was deployed to measure the optical and microphysical properties of MDs near dust source regions in Wuwei, Zhangye, and Dunhuang (in chronological order) along the Hexi Corridor over northwestern China. Throughout this dust campaign, the hourly averaged (±standard deviation) aerosol scattering coefficients (σsp, 550 nm) of the particulates with aerodynamic diameters less than 2.5 µm (PM2.5) at these three sites were sequentially 101.5 ± 36.8, 182.2 ± 433.1, and 54.0 ± 32.0 Mm−1. Correspondingly, the absorption coefficients (σap, 637 nm) were 9.7 ± 6.1, 6.0 ± 4.6, and 2.3 ± 0.9 Mm−1; single-scattering albedos (ω, 637 nm) were 0.902 ± 0.025, 0.931 ± 0.037, and 0.949 ± 0.020; and scattering Ångström exponents (Åsp, 450–700 nm) of PM2.5 were 1.28 ± 0.27, 0.77 ± 0.51, and 0.52 ± 0.31. During a severe dust storm in Zhangye (i.e., from 23 to 25 April), the highest values of σsp2.5 (∼ 5074 Mm−1), backscattering coefficient (σbsp2.5, ∼ 522 Mm−1), and ω637 (∼ 0.993) and the lowest values of backscattering fraction (b2.5, ∼ 0.101) at 550 nm and Åsp2.5 (∼ −0.046) at 450–700 nm, with peak values of aerosol number size distribution (appearing at the particle diameter range of 1–3 µm), exhibited that the atmospheric aerosols were dominated by coarse-mode dust aerosols. It is hypothesized that the relatively higher values of mass scattering efficiency during floating dust episodes in Wuwei and Zhangye are attributed to the anthropogenic soil dust produced by agricultural cultivations.


2013 ◽  
Vol 6 (4) ◽  
pp. 991-1016 ◽  
Author(s):  
F. Waquet ◽  
C. Cornet ◽  
J.-L. Deuzé ◽  
O. Dubovik ◽  
F. Ducos ◽  
...  

Abstract. 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-mode particle size cannot be accurately retrieved with the present polarization measurements. Our complete and accurate algorithm cannot be applied to process large amounts of data, so a simpler algorithm was developed to retrieve the AOT and the Ångström exponent above clouds in an operational way. Illustrations are provided for July–August 2008 near the African coast. Large mean AOTs above clouds at 0.865 μm (>0.3) are retrieved for oceanic regions near the coasts of South Africa that correspond to biomass-burning aerosols, whereas even larger mean AOTs above clouds for mineral dust particles (>0.6) are also retrieved near the coasts of Senegal. For these regions and time period, the direct AAC radiative forcing is likely to be significant. The final aim of this work is the global monitoring of the AAC properties and the estimation of the direct aerosol radiative forcing in cloudy scenes.


2015 ◽  
Vol 8 (9) ◽  
pp. 9289-9338 ◽  
Author(s):  
M. J. Granados-Muñoz ◽  
J. A. Bravo-Aranda ◽  
D. Baumgardner ◽  
J. L. Guerrero-Rascado ◽  
D. Pérez-Ramírez ◽  
...  

Abstract. In this work we present an analysis of mineral dust optical and microphysical properties obtained from different retrieval techniques applied to active and passive remote sensing measurements, including a comparison with simultaneous in-situ aircraft measurements. Data were collected in a field campaign performed during a mineral dust outbreak a Granada, Spain, experimental site (37.16° N, 3.61° W, 680 m a.s.l.) on the 27 June 2011. Column-integrated properties are provided by sun- and star-photometry which allows a continuous evaluation of the mineral dust optical properties during both day and night-time. Both the Linear Estimation and AERONET (Aerosol Robotic Network) inversion algorithms are applied for the retrieval of the column-integrated microphysical particle properties. In addition, vertically-resolved microphysical properties are obtained from a multi-wavelength Raman lidar system included in EARLINET (European Aerosol Research Lidar Network), by using both LIRIC (Lidar Radiometer Inversion Code) algorithm during daytime and an algorithm applied to the Raman measurements based on the regularization technique during night-time. LIRIC retrievals reveal several dust layers between 3 and 5 km a.s.l. with volume concentrations of the coarse spheroid mode up to 60 μm3 cm−3. The combined use of the regularization and LIRIC methods reveals the night-to-day evolution of the vertical structure of the mineral dust microphysical properties and offers complementary information to that from column-integrated variables retrieved from passive remote sensing. Additionally, lidar depolarization profiles and LIRIC retrieved volume concentration are compared with aircraft in-situ measurements. This study presents for the first time a comparison of both volume concentration and dust particle polarization ratios measured with in-situ and remote sensing techniques. Results for the depolarization measurements in the dust layer indicate reasonable agreement within the estimated uncertainties. The differences in the volume concentration profiles, although somewhat larger, are still within the expected uncertainties.


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