14 research outputs found

    The unprecedented 2017-2018 stratospheric smoke event : Decay phase and aerosol properties observed with the EARLINET

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    © Author(s) 2019. This open access work is distributed under the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/).Six months of stratospheric aerosol observations with the European Aerosol Research Lidar Network (EARLINET) from August 2017 to January 2018 are presented. The decay phase of an unprecedented, record-breaking stratospheric perturbation caused by wildfire smoke is reported and discussed in terms of geometrical, optical, and microphysical aerosol properties. Enormous amounts of smoke were injected into the upper troposphere and lower stratosphere over fire areas in western Canada on 12 August 2017 during strong thunderstorm-pyrocumulonimbus activity. The stratospheric fire plumes spread over the entire Northern Hemisphere in the following weeks and months. Twenty-eight European lidar stations from northern Norway to southern Portugal and the eastern Mediterranean monitored the strong stratospheric perturbation on a continental scale. The main smoke layer (over central, western, southern, and eastern Europe) was found at heights between 15 and 20 km since September 2017 (about 2 weeks after entering the stratosphere). Thin layers of smoke were detected at heights of up to 22-23 km. The stratospheric aerosol optical thickness at 532 nm decreased from values > 0.25 on 21-23 August 2017 to 0.005-0.03 until 5-10 September and was mainly 0.003-0.004 from October to December 2017 and thus was still significantly above the stratospheric background (0.001-0.002). Stratospheric particle extinction coefficients (532 nm) were as high as 50-200 Mm-1 until the beginning of September and on the order of 1 Mm-1 (0.5- 5 Mm-1) from October 2017 until the end of January 2018. The corresponding layer mean particle mass concentration was on the order of 0.05-0.5 Όg m-3 over these months. Soot particles (light-absorbing carbonaceous particles) are efficient ice-nucleating particles (INPs) at upper tropospheric (cirrus) temperatures and available to influence cirrus formation when entering the tropopause from above. We estimated INP concentrations of 50-500 L-1 until the first days in September and afterwards 5-50 L-1 until the end of the year 2017 in the lower stratosphere for typical cirrus formation temperatures of -55 ?C and an ice supersaturation level of 1.15. The measured profiles of the particle linear depolarization ratio indicated a predominance of nonspherical smoke particles. The 532 nm depolarization ratio decreased slowly with time in the main smoke layer from values of 0.15-0.25 (August-September) to values of 0.05-0.10 (October-November) and < 0.05 (December-January). The decrease of the depolarization ratio is consistent with aging of the smoke particles, growing of a coating around the solid black carbon core (aggregates), and thus change of the shape towards a spherical form. We found ascending aerosol layer features over the most southern European stations, especially over the eastern Mediterranean at 32-35? N, that ascended from heights of about 18-19 to 22-23 km from the beginning of October to the beginning of December 2017 (about 2 km per month). We discuss several transport and lifting mechanisms that may have had an impact on the found aerosol layering structures.Peer reviewe

    EARLINET evaluation of the CATS Level 2 aerosol backscatter coefficient product

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    We present the evaluation activity of the European Aerosol Research Lidar Network (EARLINET) for the quantitative assessment of the Level 2 aerosol backscatter coefficient product derived by the Cloud-Aerosol Transport System (CATS) aboard the International Space Station (ISS; Rodier et al., 2015). The study employs correlative CATS EARLINET backscatter measurements within a 50 km distance between the ground station and the ISS overpass and as close in time as possible, typically with the starting time or stopping time of the EARLINET performed asurement time window within 90 min of the ISS overpass, for the period from February 2015 to September 2016

    Towards a Multi-Instrumental Approach to Closing Aerosol Optical Extinction Profiles

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    A novel methodology is formulated and investigated on test cases for the reconstruction of complete vertical aerosol extinction profiles in which a synergy of remote, in-situ, and airborne measurements is utilized. The GRASP Open aerosol retrieval algorithm is supplied with remote LIDAR and sunphotometer data to obtain aerosol extinction profiles within the LIDAR&rsquo;s operation range for coarse and fine aerosol modes separately. These are supplemented with ground-based in-situ measurements of particle size distribution that are translated to coarse and fine aerosol extinction coefficients with the use of Mie theory. UAV-based observations with optical particle counters are included to add information on vertical aerosol variability in the near-surface region. The profiles are closed with an analytical interpolation that is fine-tuned to produce continuous and smooth extinction profiles throughout the whole troposphere that are in agreement with columnar aerosol optical depth measurements. We present the possibility of reconstructing a complete and calibrated aerosol extinction profile, based on the case studies at a Central European background station. We include data-denial experiments to show that the inclusion of UAV-based measurements improves such reconstructions by providing crucial information on aerosol profiles near the ground. The proposed methodology can prove to be a potent tool for studies of aerosol concentration and evolution, especially when the majority of the pollution resides near the surface. Such conditions are prevalent in many highly industrialized regions, including central and southern Poland

    Impact of Vertical Profiles of Aerosols on the Photolysis Rates in the Lower Troposphere from the Synergy of Photometer and Ceilometer Measurements in Raciborz, Poland, for the Period 2015&ndash;2020

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    The effect of the aerosol vertical distribution on photolysis frequencies of O3 and NO2 is studied. Aerosol measurements in Raciborz (50.08&deg; N, 18.19&deg; E), Poland, made using the CIMEL Sun photometer and collocated CHM-15k &ldquo;Nimbus&rdquo; ceilometer are analyzed for the period 2015&ndash;2020. Vertical profiles of the aerosol extinction are derived from the Generalized Retrieval of Atmosphere and Surface Properties (GRASP) algorithm combining the ceilometer measurements of the aerosol backscattering coefficient with the collocated CIMEL measurements of the columnar characteristics of aerosols. The photolysis frequencies are calculated at the three levels in the lower troposphere (the surface and 0.5 and 2 km above the surface) using a radiative transfer model, Tropospheric Ultraviolet and Visible (TUV), for various settings of aerosol optical properties in the model input. The importance of the aerosol vertical distribution on photolysis frequencies is inferred by analyzing statistics of the differences between the output of the model, including the extinction profile from the GRASP algorithm, and the default TUV model (based on columnar aerosol characteristics by the CIMEL Sun photometer and Elterman&rsquo;s extinction profile). For model levels above the surface, standard deviation, 2.5th percentile, 97.5th percentile, and the extremes, calculated from relative differences between these input settings, are comparable with the pertaining statistical values for the input pair providing changes of photolysis frequencies only due to the variability of the columnar aerosol characteristics. This indicates that the vertical properties of aerosols affect the distribution of the photolysis frequencies in the lower troposphere on a similar scale to that due to variations in columnar aerosol characteristics

    Ozone Formation during Photocatalytic Oxidation of Nitric Oxides under UV Irradiation with the Use of Commercial TiO2 Photocatalytic Powders

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    The application of photocatalytic materials has been intensively researched in recent decades. The process of nitric oxide (NO) oxidation during photocatalysis has been observed to result in the formation of nitric dioxide (NO2). This is a significant factor of the photocatalysis process, as NO2 is more toxic than NO. However, it has been reported that ozone (O3) is also formed during the photocatalytic reaction. This study analyzed the formation and oxidationof O3 during the photocatalytic oxidation of NO under ultraviolet irradiation using commercial photocatalytic powders: AEROXIDE&reg; TiO2 P25 by Evonik, KRONOClean&reg; 7050 by KRONOS&reg;, and KRONOClean&reg; 7000 by KRONOS&reg;. An NO concentration of 100 ppb was assumed in laboratory tests based on the average nitric oxide concentrations recorded by the monitoring station in Warsaw. A mix flow-type reactor was applied in the study, and the appropriateness of its application was verified using a numerical model. The developed model assumed an empty reactor without a photocatalytic material, as well as a reactor with a photocatalytic material at its bottom to verify the gas flow in the chamber. The analysis of the air purification performance of photocatalytic powders indicated a significant reduction of NO and NOx and typical NO2 formation. However, no significant formation of O3 was observed. This observation was verified by the oxidation of pure ozone in the process of photocatalysis. The results indicated the oxidation of ozone concentration during the photocatalytic reaction, but self-decomposition of a significant amount of the gas

    Modification of Local Urban Aerosol Properties by Long-Range Transport of Biomass Burning Aerosol

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    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 PM2.5. 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

    Modification of Local Urban Aerosol Properties by Long-Range Transport of Biomass Burning Aerosol

    Get PDF
    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 PM2.5. 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
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