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The direct and indirect radiation forcing of aerosol particles deeply affect the energy budget and the atmospheric chemical and physical processes. To retrieve the vertical aerosol mass fluxes and to investigate the vertical transport process of aerosol by a coherent Doppler lidar (CDL), a practical method for instrumental calibration and aerosol optical properties retrieval based on CDL and sun photometer synchronization observations has been developed. A conversion of aerosol optical properties to aerosol microphysical properties is achieved by applying a well-developed algorithm. Furthermore, combining the vertical velocity measured simultaneously with a CDL, we use the eddy covariance (EC) method to retrieve the vertical turbulent aerosol mass fluxes by a CDL and sun photometer with a spatial resolution of 15 m and a temporal resolution of 1 s throughout the planetary boundary layer (PBL). In this paper, we present a measurement case of 24-h continuous fluxes observations and analyze the diurnal variation of the vertical velocity, the aerosol backscatter coefficient at 1550 nm, the mean aerosol mass concentration, and the vertical aerosol mass fluxes on 13 April 2020. Finally, the main relative errors in aerosol mass flux retrieval, including sample error σF,S, aerosol optical properties retrieval error σF,R, and error introduced from aerosol microphysical properties retrieval algorithm σF,I, are evaluated. The sample error σF,S is the dominating error which increases with height except during 12:00–13:12 LST. The aerosol optical properties retrieval error σF,R is 21% and the error introduced from the aerosol microphysical properties retrieval algorithm σF,I is less than 50%.

Pollution haze is a frequent phenomenon in the North China Plain (NCP) appearing during winter when the aerosol is affected by various pollutant sources and has complex distribution of the aerosol properties, while different aerosol components may have various critical effects on air quality, human health and radiative balance. Therefore, large-scale and accurate aerosol components characterization is urgently and highly desirable but hardly achievable at the regional scale. In this respect, directional and polarimetric remote sensing observations have great potential for providing information about the aerosol components. In this study, a state-of-the-art GRASP/Component approach was employed for attempting to characterize aerosol components in the NCP using POLDER/PARASOL satellite observations. The analysis was done for January 2012 in Beijing (BJ) and Shanxi (SX). The results indicate a peak of the BC mass concentration in an atmospheric column of 82.8 mg/m2 in the SX region, with a mean of 29.2 mg/m2 that is about four times higher than one in BJ (8.9 mg/m2). The mean BrC mass concentrations are, however, higher in BJ (up to ca. 271 mg/m2) than that in SX, which can be attributed to a higher anthropogenic emission. The mean amount of fine ammonium sulfate-like particles observed in the BJ region was three times lower than in SX (131 mg/m2). The study also analyzes meteorological and air quality data for characterizing the pollution event in BJ. During the haze episode, the results suggest a rapid increase in the fine mode aerosol volume concentration associated with a decrease of a scale height of aerosol down to 1500 m. As expected, the values of aerosol optical depth (AOD), absorbing aerosol optical depth (AAOD) and fine mode aerosol optical depth (AODf) are much higher on hazy days. The mass fraction of ammonium sulfate-like aerosol increases from about 13% to 29% and mass concentration increases from 300 mg/m2 to 500 mg/m2. The daily mean PM2.5 concentration and RH independently measured during these reported pollution episodes reach up to 425 g/m3 and 80% correspondingly. The monthly mean mass concentrations of other aerosol components in the BJ are found to be in agreement with the results of previous research works. Finally, a preliminary comparison of these remote sensing derived results with literature and in situ PM2.5 measurements is also presented.

The impact of aerosol spatio-temporal variability on the Arctic radiative budget is not fully constrained. This case study focuses on the intra-Arctic modification of long-range transported aerosol and its direct aerosol radiative effect (ARE). Different types of air-borne and ground-based remote sensing observations (from Lidar and sun-photometer) revealed a high tropospheric aerosol transport episode over two parts of the European Arctic in April 2018. By incorporating the derived aerosol optical and microphysical properties into a radiative transfer model, we assessed the ARE over the two locations. Our study displayed that even in neighboring Arctic upper tropospheric levels, aged aerosol was transformed due to the interplay of removal processes (nucleation scavenging and dry deposition) and alteration of the aerosol source regions (northeast Asia and north Europe). Along the intra-Arctic transport, the coarse aerosol mode was depleted and the visible wavelength Lidar ratio (LR) increased significantly (from 15 to 64–82 sr). However, the aerosol modifications were not reflected on the ARE. More specifically, the short-wave (SW) atmospheric column ARE amounted to +4.4 - +4.9 W m−2 over the ice-covered Fram Strait and +4.5 W m−2 over the snow-covered Ny-Ålesund. Over both locations, top-of-atmosphere (TOA) warming was accompanied by surface cooling. These similarities can be attributed to the predominant accumulation mode, which drives the SW radiative budget, as well as to the similar layer altitude, solar geometry, and surface albedo conditions over both locations. However, in the context of retreating sea ice, the ARE may change even along individual transport episodes due to the ice albedo feedback.

This work evaluates the Lidar-Radiometer Inversion Code (LIRIC) using sun-sky photometers located at different altitudes in the same atmospheric column. Measurements were acquired during an intensive observational period in summer 2012 at Aerosols, Clouds, and Trace gases Research InfraStructure Network (ACTRIS)/Aerosol Robotic Network (AERONET) Granada (GRA; 37.16°N, 3.61°W, 680 m above sea level (a.s.l.)) and Cerro Poyos (CP; 37.11°N, 3.49°W, 1820 m a.s.l.) sites. Both stations operated AERONET sun-photometry, with an additional lidar system operating at Granada station. The extended database of simultaneous lidar and sun-photometry measurements from this study allowed the statistical analysis of vertically resolved microphysical properties retrieved with LIRIC, with 70% of the analyzed cases corresponding to mineral dust. Consequently, volume concentration values were 46 μm3/cm3 on average, with a value of ~30 μm3/cm3 corresponding to the coarse spheroid mode and concentrations below 10 μm3/cm3 for the fine and coarse spherical modes. According to the microphysical properties’ profiles, aerosol particles reached altitudes up to 6000 m a.s.l., as observed in previous studies over the same region. Results obtained from comparing the LIRIC retrievals from GRA and from CP revealed good agreement between both stations with differences within the expected uncertainties associated with LIRIC (15%). However, larger discrepancies were found for 10% of the cases, mostly due to the incomplete overlap of the lidar signal and/or to the influence of different aerosol layers advected from the local origin located between both stations, which is particularly important in cases of low aerosol loads. Nevertheless, the results presented here demonstrate the robustness and self-consistency of LIRIC and consequently its applicability to large databases such as those derived from ACTRIS-European Aerosol Research Lidar Network (EARLINET) observations.