2009, Zeller, O., Bremer, J.

The dependence of mesospheric VHF radar echoes during summer months on geomagnetic activity has been investigated with observation data of the OSWIN radar in Kühlungsborn (54° N) and of the ALWIN radar in Andenes (69° N). Using daily mean values of VHF radar echoes and of geomagnetic activity indices in superimposed epoch analyses, the comparison of both data sets shows in general stronger radar echoes on the day of the maximum geomagnetic activity, the maximum value one day after the geomagnetic disturbance, and enhanced radar echoes also on the following 2–3 days. This phenomenon is observed at middle and polar latitudes and can be explained by precipitating particle fluxes during the ionospheric post storm effect. At polar latitudes, the radar echoes decrease however during and one day after very strong geomagnetic disturbances. The possible reason of this surprising effect is discussed.

2006, Boy, M., Hellmuth, O., Korhonen, H., Nilsson, E.D., ReVelle, D., Turnipseed, A., Arnold, F., Kulmala, M.

The manuscript presents a detailed description of the meteorological and chemical code of Malte – a model to predict new aerosol formation in the lower troposphere. The aerosol dynamics are achieved by the new developed UHMA (University of Helsinki Multicomponent Aerosol Model) code with kinetic limited nucleation as responsible mechanism to form new clusters. First results indicate that the model is able to predict the on- and offset of new particle formation as well as the total aerosol number concentrations that were in good agreement with the observations. Further, comparison of predicted and measured H2SO4 concentrations showed a satisfactory agreement. The simulation results indicated that at a certain transitional particle diameter (2–7 nm), organic molecules can begin to contribute significantly to the growth rate compared to sulphuric acid. At even larger particle sizes, organic molecules can dominate the growth rate on days with significant monoterpene concentrations. The intraday vertical evolution of newly formed clusters and particles in two different size ranges resulted in two maxima at the ground. These particles grow around noon to the detectable size range and agree well with measured vertical profiles.

2015, Crenn, V., Sciare, J., Croteau, P.L., Verlhac, S., Fröhlich, R., Belis, C.A., Aas, W., Äijälä, M., Alastuey, A., Artiñano, B., Baisnée, D., Bonnaire, N., Bressi, M., Canagaratna, M., Canonaco, F., Carbone, C., Cavalli, F., Coz, E., Cubison, M.J., Esser-Gietl, J.K., Green, D.C., Gros, V., Heikkinen, L., Herrmann, H., Lunder, C., Minguillón, M.C., Močnik, G., O'Dowd, C.D., Ovadnevaite, J., Petit, J.-E., Petralia, E., Poulain, L., Priestman, M., Riffault, V., Ripoll, A., Sarda-Estève, R., Slowik, J.G., Setyan, A., Wiedensohler, A., Baltensperger, U., Prévôt, A.S.H., Jayne, J.T., Favez, O.

As part of the European ACTRIS project, the first large Quadrupole Aerosol Chemical Speciation Monitor (Q-ACSM) intercomparison study was conducted in the region of Paris for 3 weeks during the late-fall – early-winter period (November–December 2013). The first week was dedicated to the tuning and calibration of each instrument, whereas the second and third were dedicated to side-by-side comparison in ambient conditions with co-located instruments providing independent information on submicron aerosol optical, physical, and chemical properties. Near real-time measurements of the major chemical species (organic matter, sulfate, nitrate, ammonium, and chloride) in the non-refractory submicron aerosols (NR-PM1) were obtained here from 13 Q-ACSM. The results show that these instruments can produce highly comparable and robust measurements of the NR-PM1 total mass and its major components. Taking the median of the 13 Q-ACSM as a reference for this study, strong correlations (r2 > 0.9) were observed systematically for each individual Q-ACSM across all chemical families except for chloride for which three Q-ACSMs showing weak correlations partly due to the very low concentrations during the study. Reproducibility expanded uncertainties of Q-ACSM concentration measurements were determined using appropriate methodologies defined by the International Standard Organization (ISO 17025, 1999) and were found to be 9, 15, 19, 28, and 36 % for NR-PM1, nitrate, organic matter, sulfate, and ammonium, respectively. However, discrepancies were observed in the relative concentrations of the constituent mass fragments for each chemical component. In particular, significant differences were observed for the organic fragment at mass-to-charge ratio 44, which is a key parameter describing the oxidation state of organic aerosol. Following this first major intercomparison exercise of a large number of Q-ACSMs, detailed intercomparison results are presented, along with a discussion of some recommendations about best calibration practices, standardized data processing, and data treatment.

2021, Córdoba-Jabonero, Carmen, Ansmann, Albert, Jiménez, Cristofer, Baars, Holger, López-Cayuela, María-Ángeles, Engelmann, Ronny

Simultaneous observations of a polarized micro-pulse lidar (P-MPL) system and two reference European Aerosol Research Lidar Network lidars running at the Leipzig site Germany, 51.4g gN, 12.4g gE; 125gmga.s.l.) were performed during a comprehensive 2-month field intercomparison campaign in summer 2019. An experimental assessment regarding both the overlap (OVP) correction of the P-MPL signal profiles and the volume linear depolarization ratio (VLDR) analysis, together with its impact on the retrieval of the aerosol optical properties, is achieved; the experimental procedure used is also described. The optimal lidar-specific OVP function is experimentally determined, highlighting that the one delivered by the P-MPL manufacturer cannot be used long. Among the OVP functions examined, the averaged function between those obtained from the comparison of the P-MPL observations with those of the other two reference lidars seems to be the best proxy at both near- and far-field ranges. In addition, the impact of the OVP function on the accuracy of the retrieved profiles of the total particle backscatter coefficient (PBC) and the particle linear depolarization ratio (PLDR) is examined. The VLDR profile is obtained and compared with that derived from the reference lidar, showing that it needs to be corrected by a small offset value with good accuracy. Once P-MPL measurements are optimally (OVP, VLDR) corrected, both the PBC and PLDR profiles can be accurately derived and are in good agreement with reference aerosol retrievals. Overall, as a systematic requirement for lidar systems, an adequate OVP function determination and VLDR testing analysis needs to be performed on a regular basis to correct the P-MPL measurements in order to derive suitable aerosol products. A dust event observed in Leipzig in June 2019 is used for illustration.

2016, Wandinger, Ulla, Freudenthaler, Volker, Baars, Holger, Amodeo, Aldo, Engelmann, Ronny, Mattis, Ina, Groß, Silke, Pappalardo, Gelsomina, Giunta, Aldo, D'Amico, Giuseppe, Chaikovsky, Anatoli, Osipenko, Fiodor, Slesar, Alexander, Nicolae, Doina, Belegante, Livio, Talianu, Camelia, Serikov, Ilya, Linné, Holger, Jansen, Friedhelm, Apituley, Arnoud, Wilson, Keith M., de Graaf, Martin, Trickl, Thomas, Giehl, Helmut, Adam, Mariana, Comerón, Adolfo, Muñoz-Porcar, Constantino, Rocadenbosch, Francesc, Sicard, Michaël, Tomás, Sergio, Lange, Diego, Kumar, Dhiraj, Pujadas, Manuel, Molero, Francisco, Fernández, Alfonso J., Alados-Arboledas, Lucas, Bravo-Aranda, Juan Antonio, Navas-Guzmán, Francisco, Guerrero-Rascado, Juan Luis, Granados-Muñoz, María José, Preißler, Jana, Wagner, Frank, Gausa, Michael, Grigorov, Ivan, Stoyanov, Dimitar, Iarlori, Marco, Rizi, Vincenco, Spinelli, Nicola, Boselli, Antonella, Wang, Xuan, Feudo, Teresa Lo, Perrone, Maria Rita, De Tomas, Ferdinando, Burlizzi, Pasquale

This paper introduces the recent European Aerosol Research Lidar Network (EARLINET) quality-assurance efforts at instrument level. Within two dedicated campaigns and five single-site intercomparison activities, 21 EARLINET systems from 18 EARLINET stations were intercompared between 2009 and 2013. A comprehensive strategy for campaign setup and data evaluation has been established. Eleven systems from nine EARLINET stations participated in the EARLINET Lidar Intercomparison 2009 (EARLI09). In this campaign, three reference systems were qualified which served as traveling standards thereafter. EARLINET systems from nine other stations have been compared against these reference systems since 2009. We present and discuss comparisons at signal and at product level from all campaigns for more than 100 individual measurement channels at the wavelengths of 355, 387, 532, and 607 nm. It is shown that in most cases, a very good agreement of the compared systems with the respective reference is obtained. Mean signal deviations in predefined height ranges are typically below ±2 %. Particle backscatter and extinction coefficients agree within ±2  ×  10−4 km−1 sr−1 and ± 0.01 km−1, respectively, in most cases. For systems or channels that showed larger discrepancies, an in-depth analysis of deficiencies was performed and technical solutions and upgrades were proposed and realized. The intercomparisons have reinforced confidence in the EARLINET data quality and allowed us to draw conclusions on necessary system improvements for some instruments and to identify major challenges that need to be tackled in the future.

2010, Thonicke, K., Spessa, A., Prentice, I.C., Harrison, S.P., Dong, L., Carmona-Moreno, C.

A process-based fire regime model (SPITFIRE) has been developed, coupled with ecosystem dynamics in the LPJ Dynamic Global Vegetation Model, and used to explore fire regimes and the current impact of fire on the terrestrial carbon cycle and associated emissions of trace atmospheric constituents. The model estimates an average release of 2.24 Pg C yr−1 as CO2 from biomass burning during the 1980s and 1990s. Comparison with observed active fire counts shows that the model reproduces where fire occurs and can mimic broad geographic patterns in the peak fire season, although the predicted peak is 1–2 months late in some regions. Modelled fire season length is generally overestimated by about one month, but shows a realistic pattern of differences among biomes. Comparisons with remotely sensed burnt-area products indicate that the model reproduces broad geographic patterns of annual fractional burnt area over most regions, including the boreal forest, although interannual variability in the boreal zone is underestimated.

2021, Cuesta-Mosquera, Andrea, Močnik, Griša, Drinovec, Luka, Müller, Thomas, Pfeifer, Sascha, Minguillón, María Cruz, Briel, Björn, Buckley, Paul, Dudoitis, Vadimas, Fernández-García, Javier, Fernández-Amado, María, Ferreira De Brito, Joel, Riffault, Veronique, Flentje, Harald, Heffernan, Eimear, Kalivitis, Nikolaos, Kalogridis, Athina-Cerise, Keernik, Hannes, Marmureanu, Luminita, Luoma, Krista, Marinoni, Angela, Pikridas, Michael, Schauer, Gerhard, Serfozo, Norbert, Servomaa, Henri, Titos, Gloria, Yus-Díez, Jesús, Zioła, Natalia, Wiedensohler, Alfred

Aerosolized black carbon is monitored worldwide to quantify its impact on air quality and climate. Given its importance, measurements of black carbon mass concentrations must be conducted with instruments operating in qualitychecked and ensured conditions to generate data which are reliable and comparable temporally and geographically. In this study, we report the results from the largest characterization and intercomparison of filter-based absorption photometers, the Aethalometer model AE33, belonging to several European monitoring networks. Under controlled laboratory conditions, a total of 23 instruments measured mass concentrations of black carbon from three wellcharacterized aerosol sources: synthetic soot, nigrosin particles, and ambient air from the urban background of Leipzig, Germany. The objective was to investigate the individual performance of the instruments and their comparability; we analyzed the response of the instruments to the different aerosol sources and the impact caused by the use of obsolete filter materials and the application of maintenance activities. Differences in the instrument-to-instrument variabilities from equivalent black carbon (eBC) concentrations reported at 880 nm were determined before maintenance activities (for soot measurements, average deviation from total least square regression was-2.0% and the range-16% to 7 %; for nigrosin measurements, average deviation was 0.4% and the range-15% to 17 %), and after they were carried out (for soot measurements, average deviation was-1.0% and the range-14% to 8 %; for nigrosin measurements, the average deviation was 0.5%and the range-12%to 15 %). The deviations are in most of the cases explained by the type of filter material employed by the instruments, the total particle load on the filter, and the flow calibration. The results of this intercomparison activity show that relatively small unit-to-unit variability of AE33-based particle light absorbing measurements is possible with wellmaintained instruments. It is crucial to follow the guidelines for maintenance activities and the use of the proper filter tape in the AE33 to ensure high quality and comparable black carbon (BC) measurements among international observational networks. © 2021 Author(s). This work is distributed under the Creative Commons Attribution 4.0 License.

2017, Nichman, Leonid, Järvinen, Emma, Dorsey, James, Connolly, Paul, Duplissy, Jonathan, Fuchs, Claudia, Ignatius, Karoliina, Sengupta, Kamalika, Stratmann, Frank, Möhler, Ottmar, Schnaiter, Martin, Gallagher, Martin

Optical probes are frequently used for the detection of microphysical cloud particle properties such as liquid and ice phase, size and morphology. These properties can eventually influence the angular light scattering properties of cirrus clouds as well as the growth and accretion mechanisms of single cloud particles. In this study we compare four commonly used optical probes to examine their response to small cloud particles of different phase and asphericity. Cloud simulation experiments were conducted at the Cosmics Leaving OUtdoor Droplets (CLOUD) chamber at European Organisation for Nuclear Research (CERN). The chamber was operated in a series of multi-step adiabatic expansions to produce growth and sublimation of ice particles at super- and subsaturated ice conditions and for initial temperatures of -30, -40 and -50°C. The experiments were performed for ice cloud formation via homogeneous ice nucleation. We report the optical observations of small ice particles in deep convection and in situ cirrus simulations. Ice crystal asphericity deduced from measurements of spatially resolved single particle light scattering patterns by the Particle Phase Discriminator mark 2 (PPD-2K, Karlsruhe edition) were compared with Cloud and Aerosol Spectrometer with Polarisation (CASPOL) measurements and image roundness captured by the 3View Cloud Particle Imager (3V-CPI). Averaged path light scattering properties of the simulated ice clouds were measured using the Scattering Intensity Measurements for the Optical detectioN of icE (SIMONE) and single particle scattering properties were measured by the CASPOL. We show the ambiguity of several optical measurements in ice fraction determination of homogeneously frozen ice in the case where sublimating quasi-spherical ice particles are present. Moreover, most of the instruments have difficulties of producing reliable ice fraction if small aspherical ice particles are present, and all of the instruments cannot separate perfectly spherical ice particles from supercooled droplets. Correlation analysis of bulk averaged path depolarisation measurements and single particle measurements of these clouds showed higher R2 values at high concentrations and small diameters, but these results require further confirmation. We find that none of these instruments were able to determine unambiguously the phase of the small particles. These results have implications for the interpretation of atmospheric measurements and parametrisations for modelling, particularly for low particle number concentration clouds.

2015, Gabler, Carolin, Zietz, Carmen, Bieck, Richard, Göhler, Rebecca, Lindner, Tobias, Haenle, Maximilian, Finke, Birgit, Meichsner, Jürgen, Testrich, Holger, Nowottnick, Mathias, Frerich, Bernhard, Bader, Rainer

A common method to derive both qualitative and quantitative data to evaluate osseointegration of implants is histomorphometry. The present study describes a new image reconstruction algorithm comparing the results of bone-to-implant contact (BIC) evaluated by means of µCT with histomorphometry data. Custom-made conical titanium alloyed (Ti6Al4V) implants were inserted in the distal tibial bone of female Sprague-Dawley rats. Different surface configurations were examined: Ti6Al4V implants with plasma-polymerized allylamine (PPAAm) coating and plasma-polymerized ethylenediamine (PPEDA) coating as well as implants without surface coating. After six weeks postoperatively, tibiae were explanted and BIC was determined by µCT (3D) and afterwards by histomorphometry (2D). In comparison to uncoated Ti6Al4V implants demonstrating low BIC of 32.4% (histomorphometry) and 51.3% (µCT), PPAAm and PPEDA coated implants showed a nonsignificant increase in BIC (histomorphometry: 45.7% and 53.5% and µCT: 51.8% and 62.0%, resp.). Mean BIC calculated by µCT was higher for all surface configurations compared to BIC detected by histomorphometry. Overall, a high correlation coefficient of 0.70 () was found between 3D and 2D quantification of BIC. The μCT analysis seems to be suitable as a nondestructive and accurate 3D imaging method for the evaluation of the bone-implant interface.

2011, Gagné, S., Lehtipalo, K., Manninen, H.E., Nieminen, T., Schobesberger, S., Franchin, A., Yli-Juuti, T., Boulon, J., Sonntag, A., Mirme, S., Mirme, A., Hõrrak, U., Petäjä, T., Asmi, E., Kulmala, M.

We evaluated 11 air ion spectrometers from Airel Ltd. after they had spent one year in field measurements as a part of the EUCAARI project: 5 Air Ion Spectrometers (AIS), 5 Neutral cluster and Air Ion Spectrometers (NAIS) and one Airborne NAIS (ANAIS). This is the first time that an ANAIS is evaluated and compared so extensively. The ion spectrometers' mobility and concentration accuracy was evaluated. Their measurements of ambient air were compared between themselves and to reference instruments: a Differential Mobility Particle Sizer (DMPS), a Balanced Scanning Mobility Analyzer (BSMA), and an Ion-DMPS. We report on the simultaneous measurement of a new particle formation (NPF) event by all 11 instruments and the 3 reference instruments. To our knowledge, it is the first time that the size distribution of ions and particles is measured by so many ion spectrometers during a NPF event. The new particle formation rates (~0.2 cm−3 s−1 for ions and ~2 cm−3 s−1 for particles) and growth rates (~25 nm h−1 in the 3–7 nm size range) were calculated for all the instruments. The NAISs and the ANAIS gave higher concentrations and formation rates than the AISs. For example, the AISs agreed with the BSMA within 11 % and 28 % for negative and positive ion concentration respectively, whereas the NAISs agreed within 23 % and 29 %. Finally, based on the results presented here, we give guidelines for data evaluation, when data from different individual ion spectrometers are compared.