This paper focuses on optical and microphysical properties of long‐range transported biomass burning (BB) aerosols and their variation with atmospheric evolution (ageing), as observed by a multiwavelength Raman lidar, part of EARLINET (European Aerosol LIdar NETwork). Chemical analysis of the atmospheric aerosol was done using a colocated aerosol mass spectrometer (AMS). One relevant optical parameter for the ageing process is the Ångström exponent. In our study, we find that it decreases from 2 for fresh to 1.4–0.5 for aged smoke particles. The ratio of lidar (extinction‐to‐backscatter) ratios (LR₅₃₂/LR₃₅₅) changes rapidly from values 1 for aged particles. The imaginary part of the refractive index is the most sensitive microphysical parameter. It decreases sharply from 0.05 to less than 0.01 for fresh and aged smoke particles, respectively. Single‐scattering albedo (SSA) varies from 0.74 to 0.98 depending on aerosol age and source. The AMS was used to measure the marker ions of wood‐burning particles during 2 days of measurements when the meteorological conditions favored the downward mixing of aerosols from lofted layers. Particle size distribution and particle effective radius from both AMS and lidar are similar, i.e., particle effective radii were approximately 0.27 µm for fresh BB aerosol particles. Microphysical aerosol properties from inversion of the lidar data agree with similar studies carried out in different regions on the globe. Our study shows that the Ångström exponent LR₅₃₂/LR₃₅₅ and the imaginary part of the refractive index can be used to clearly distinguish between fresh and aged smoke particles.

Multi-wavelength depolarization Raman lidar measurements from Magurele, Romania are used in this study along with simulated mass-extinction efficiencies to calculate the mass concentration profiles of different atmospheric components, due to their different depolarization contribution to the 532 nm backscatter coefficient. Linear particle depolarization ratio (δ^part) was computed using the relative amplification factor and the system-dependent molecular depolarization. The low depolarizing component was considered as urban/smoke, with a mean δ^part of 3%, while for the high depolarizing component (mineral dust) a mean δ^part of 35% was assumed. For this study 11 months of lidar measurements were analysed. Two study cases are presented in details: one for a typical Saharan dust aerosol intrusion, 10 June 2012 and one for 12 July 2012 when a lofted layer consisting of biomass burning smoke extended from 3 to 4.5 km height. Optical Properties of Aerosols and Clouds software package (OPAC) classification and conversion factors were used to calculate mass concentrations. We found that calibrated depolarization measurements are critical in distinguishing between smoke-reach aerosol during the winter and dust-reach aerosol during the summer, as well as between elevated aerosol layers having different origins. Good agreement was found between lidar retrievals and DREAM- Dust REgional Atmospheric Model forecasts in cases of Saharan dust. Our method was also compared against LIRIC (The Lidar/Radiometer Inversion Code) and very small differences were observed.

Particle depolarization ratio retrieved from lidar measurements are commonly used for aerosol-typing studies, microphysical inversion, or mass concentration retrievals. The particle depolarization ratio is one of the primary parameters that can differentiate several major aerosol components but only if the measurements are accurate enough. The accuracy related to the retrieval of particle depolarization ratios is the driving factor for assessing and improving the uncertainties of the depolarization products. This paper presents different depolarization calibration procedures used to improve the quality of the depolarization data. The results illustrate a significant improvement of the depolarization lidar products for all the selected lidar stations that have implemented depolarization calibration procedures. The calibrated volume and particle depolarization profiles at 532 nm show values that fall within a range that is generally accepted in the literature.

In the framework of the ESA-NASA Joint Aeolus Tropical Atlantic Campaign (JATAC), the ASKOS experiment was implemented during the summer and autumn of 2021 and 2022. ASKOS comprised roughly 9 weeks of measurements in the Saharan dust outflow towards the North Atlantic, with operations conducted from the Cabo Verde Islands. Through its unprecedented dataset of synergistic measurements in the region, ASKOS will allow for the calibration and validation of the aerosol/cloud product from Aeolus and the preparation of the terrain for EarthCARE cal/val activities. Moreover, ASKOS marks a turning point in our ability to study Saharan dust properties and the processes affecting its atmospheric transport, as well as the link to other components of the Earth’s system, such as the effect of dust particles on cloud formation over the Eastern Atlantic and the effect of large and giant particles on radiation. This is possible through the synergy of diverse observations acquired during the experiment, which include intense 24/7 ground-based aerosol, cloud, wind, and radiation remote sensing measurements, and UAV-based aerosol in situ measurements within the Saharan air layer, up to 5.3 km altitude, offering particle size-distributions up to 40 μm as well as sample collection for mineralogical analysis. We provide an outline of the novel measurements along with the main scientific objectives of ASKOS. The campaign data will be publicly available by September of 2023 through the EVDC portal (ESA Validation Data Center).

During August 2016, a quasi-stationary high-pressure system spreading over Central and North-Eastern Europe, caused weather conditions that allowed for 24/7 observations of aerosol optical properties by using a complex multi-wavelength PollyXT lidar system with Raman, polarization and water vapour capabilities, based at the European Aerosol Research Lidar Network (EARLINET network) urban site in Warsaw, Poland. During 24–30 August 2016, the lidar-derived products (boundary layer height, aerosol optical depth, Ångström exponent, lidar ratio, depolarization ratio) were analysed in terms of air mass transport (HYSPLIT model), aerosol load (CAMS data) and type (NAAPS model) and confronted with active and passive remote sensing at the ground level (PolandAOD, AERONET, WIOS-AQ networks) and aboard satellites (SEVIRI, MODIS, CATS sensors). Optical properties for less than a day-old fresh biomass burning aerosol, advected into Warsaw’s boundary layer from over Ukraine, were compared with the properties of long-range transported 3–5 day-old aged biomass burning aerosol detected in the free troposphere over Warsaw. Analyses of temporal changes of aerosol properties within the boundary layer, revealed an increase of aerosol optical depth and Ångström exponent accompanied by an increase of surface PM₁₀ and PM_2.5. Intrusions of advected biomass burning particles into the urban boundary layer seem to affect not only the optical properties observed but also the top height of the boundary layer, by moderating its increase.

The Airborne ROmanian Measurements of Aerosols and Trace gases (AROMAT) campaigns took place in Romania in September 2014 and August 2015. They focused on two sites: the Bucharest urban area and large power plants in the Jiu Valley. The main objectives of the campaigns were to test recently developed airborne observation systems dedicated to air quality studies and to verify their applicability for the validation of space-borne atmospheric missions such as the TROPOspheric Monitoring Instrument (TROPOMI)/Sentinel-5 Precursor (S5P). We present the AROMAT campaigns from the perspective of findings related to the validation of tropospheric NO₂, SO₂, and H₂CO. We also quantify the emissions of NO_x and SO₂ at both measurement sites. We show that tropospheric NO₂ vertical column density (VCD) measurements using airborne mapping instruments are well suited for satellite validation in principle. The signal-to-noise ratio of the airborne NO₂ measurements is an order of magnitude higher than its space-borne counterpart when the airborne measurements are averaged at the TROPOMI pixel scale. However, we show that the temporal variation of the NO₂ VCDs during a flight might be a significant source of comparison error. Considering the random error of the TROPOMI tropospheric NO₂ VCD (σ), the dynamic range of the NO₂ VCDs field extends from detection limit up to 37 σ (2.6×10¹⁶ molec. cm⁻²) and 29 σ (2×10¹⁶ molec. cm⁻²) for Bucharest and the Jiu Valley, respectively. For both areas, we simulate validation exercises applied to the TROPOMI tropospheric NO₂ product. These simulations indicate that a comparison error budget closely matching the TROPOMI optimal target accuracy of 25 % can be obtained by adding NO₂ and aerosol profile information to the airborne mapping observations, which constrains the investigated accuracy to within 28 %. In addition to NO₂, our study also addresses the measurements of SO₂ emissions from power plants in the Jiu Valley and an urban hotspot of H₂CO in the centre of Bucharest. For these two species, we conclude that the best validation strategy would consist of deploying ground-based measurement systems at well-identified locations.