2020, Laj, Paolo, Bigi, Alessandro, Rose, Clémence, Andrews, Elisabeth, Lund Myhre, Cathrine, Collaud Coen, Martine, Lin, Yong, Wiedensohler, Alfred, Schulz, Michael, Ogren, John A., Fiebig, Markus, Prenni, Anthony, Reisen, Fabienne, Romano, Salvatore, Sellegri, Karine, Sharma, Sangeeta, Schauer, Gerhard, Sheridan, Patrick, Sherman, James Patrick, Schütze, Maik, Schwerin, Andreas, Tuch, Thomas, Sohmer, Ralf, Sorribas, Mar, Steinbacher, Martin, Sun, Junying, Titos, Gloria, Toczko, Barbara, Tulet, Pierre, Tunved, Peter, Vakkari, Ville, Velarde, Fernando, Velasquez, Patricio, Villani, Paolo, Vratolis, Sterios, Wang, Sheng-Hsiang, Weinhold, Kay, Gliß, Jonas, Weller, Rolf, Yela, Margarita, Yus-Diez, Jesus, Zdimal, Vladimir, Zieger, Paul, Zikova, Nadezda, Mortier, Augustin, Pandolfi, Marco, Petäja, Tuukka, Kim, Sang-Woo, Aas, Wenche, Putaud, Jean-Philippe, Mayol-Bracero, Olga, Keywood, Melita, Labrador, Lorenzo, Aalto, Pasi, Ahlberg, Erik, Alados Arboledas, Lucas, Alastuey, Andrés, Andrade, Marcos, Artíñano, Begoña, Ausmeel, Stina, Arsov, Todor, Asmi, Eija, Backman, John, Baltensperger, Urs, Bastian, Susanne, Bath, Olaf, Beukes, Johan Paul, Brem, Benjamin T., Bukowiecki, Nicolas, Conil, Sébastien, Couret, Cedric, Day, Derek, Dayantolis, Wan, Degorska, Anna, Eleftheriadis, Konstantinos, Fetfatzis, Prodromos, Favez, Olivier, Flentje, Harald, Gini, Maria I., Gregorič, Asta, Gysel-Beer, Martin, Hallar, A. Gannet, Hand, Jenny, Hoffer, Andras, Hueglin, Christoph, Hooda, Rakesh K., Hyvärinen, Antti, Kalapov, Ivo, Kalivitis, Nikos, Kasper-Giebl, Anne, Kim, Jeong Eun, Kouvarakis, Giorgos, Kranjc, Irena, Krejci, Radovan, Kulmala, Markku, Labuschagne, Casper, Lee, Hae-Jung, Lihavainen, Heikki, Lin, Neng-Huei, Löschau, Gunter, Luoma, Krista, Marinoni, Angela, Martins Dos Santos, Sebastiao, Meinhardt, Frank, Merkel, Maik, Metzger, Jean-Marc, Mihalopoulos, Nikolaos, Nguyen, Nhat Anh, Ondracek, Jakub, Pérez, Noemi, Perrone, Maria Rita, Petit, Jean-Eudes, Picard, David, Pichon, Jean-Marc, Pont, Veronique, Prats, Natalia

Aerosol particles are essential constituents of the Earth's atmosphere, impacting the earth radiation balance directly by scattering and absorbing solar radiation, and indirectly by acting as cloud condensation nuclei. In contrast to most greenhouse gases, aerosol particles have short atmospheric residence times, resulting in a highly heterogeneous distribution in space and time. There is a clear need to document this variability at regional scale through observations involving, in particular, the in situ near-surface segment of the atmospheric observation system. This paper will provide the widest effort so far to document variability of climate-relevant in situ aerosol properties (namely wavelength dependent particle light scattering and absorption coefficients, particle number concentration and particle number size distribution) from all sites connected to the Global Atmosphere Watch network. High-quality data from almost 90 stations worldwide have been collected and controlled for quality and are reported for a reference year in 2017, providing a very extended and robust view of the variability of these variables worldwide. The range of variability observed worldwide for light scattering and absorption coefficients, single-scattering albedo, and particle number concentration are presented together with preliminary information on their long-term trends and comparison with model simulation for the different stations. The scope of the present paper is also to provide the necessary suite of information, including data provision procedures, quality control and analysis, data policy, and usage of the ground-based aerosol measurement network. It delivers to users of the World Data Centre on Aerosol, the required confidence in data products in the form of a fully characterized value chain, including uncertainty estimation and requirements for contributing to the global climate monitoring system.

2016, Baars, Holger, Kanitz, Thomas, Engelmann, Ronny, Althausen, Dietrich, Heese, Birgit, Komppula, Mika, Preißler, Jana, Tesche, Matthias, Ansmann, Albert, Wandinger, Ulla, Lim, Jae-Hyun, Ahn, Joon Young, Stachlewska, Iwona S., Amiridis, Vassilis, Marinou, Eleni, Seifert, Patric, Hofer, Julian, Skupin, Annett, Schneider, Florian, Bohlmann, Stephanie, Foth, Andreas, Bley, Sebastian, Pfüller, Anne, Giannakaki, Eleni, Lihavainen, Heikki, Viisanen, Yrjö, Hooda, Rakesh Kumar, Pereira, Sérgio Nepomuceno, Bortol, Daniele, Wagner, Frank, Mattis, Ina, Janicka, Lucja, Markowicz, Krzysztof M., Achtert, Peggy, Artaxo, Paulo, Pauliquevis, Theotonio, Souza, Rodrigo A.F., Sharma, Ved Prakesh, van Zyl, Pieter Gideon, Beukes, Johan Paul, Sun, Junying, Rohwer, Erich G., Deng, Ruru, Mamouri, Rodanthi-Elisavet, Zamorano, Felix

A global vertically resolved aerosol data set covering more than 10 years of observations at more than 20 measurement sites distributed from 63° N to 52° S and 72° W to 124° E has been achieved within the Raman and polarization lidar network PollyNET. This network consists of portable, remote-controlled multiwavelength-polarization-Raman lidars (Polly) for automated and continuous 24/7 observations of clouds and aerosols. PollyNET is an independent, voluntary, and scientific network. All Polly lidars feature a standardized instrument design with different capabilities ranging from single wavelength to multiwavelength systems, and now apply unified calibration, quality control, and data analysis. The observations are processed in near-real time without manual intervention, and are presented online at http://polly.tropos.de/. The paper gives an overview of the observations on four continents and two research vessels obtained with eight Polly systems. The specific aerosol types at these locations (mineral dust, smoke, dust-smoke and other dusty mixtures, urban haze, and volcanic ash) are identified by their Ångström exponent, lidar ratio, and depolarization ratio. The vertical aerosol distribution at the PollyNET locations is discussed on the basis of more than 55 000 automatically retrieved 30 min particle backscatter coefficient profiles at 532 nm as this operating wavelength is available for all Polly lidar systems. A seasonal analysis of measurements at selected sites revealed typical and extraordinary aerosol conditions as well as seasonal differences. These studies show the potential of PollyNET to support the establishment of a global aerosol climatology that covers the entire troposphere.

2015, Kecorius, Simonas, Kivekäs, Niku, Kristensson, Adam, Tuch, Thomas, Covert, David S., Birmili, Wolfram, Lihavainen, Heikki, Hyvärinen, Antti-Pekka, Martinsson, Johan, Sporre, Moa K., Swietlicki, Erik, Wiedensohler, Alfred, Ulevicius, Vidmantas

In this study, we evaluated 10 months data (September 2009 to June 2010) of atmospheric aerosol particle number size distribution at three atmospheric observation stations along the Baltic Sea coast: Vavihill (upwind, Sweden), Utö (upwind, Finland), and Preila (downwind, Lithuania). Differences in aerosol particle number size distributions between the upwind and downwind stations during situations of connected atmospheric flow, when the air passed each station, were used to assess the contribution of ship emissions to the aerosol number concentration (diameter interval 50–400 nm) in the Lithuanian background coastal environment. A clear increase in particle number concentration could be noticed, by a factor of 1.9 from Utö to Preila (the average total number concentration at Utö was 791 cm−3), and by a factor of 1.6 from Vavihill to Preila (the average total number concentration at Vavihill was 998 cm−3). The simultaneous measurements of absorption Ångström exponents close to unity at Preila supported our conclusion that ship emissions in the Baltic Sea contributed to the increase in particle number concentration at Preila.

2018, Nieminen, Tuomo, Kerminen, Veli-Matti, Petäjä, Tuukka, Aalto, Pasi P., Arshinov, Mikhail, Asmi, Eija, Baltensperger, Urs, Beddows, David C. S., Beukes, Johan Paul, Collins, Don, Ding, Aijun, Harrison, Roy M., Henzing, Bas, Hooda, Rakesh, Hu, Min, Hõrrak, Urmas, Kivekäs, Niku, Komsaare, Kaupo, Krejci, Radovan, Kristensson, Adam, Laakso, Lauri, Laaksonen, Ari, Leaitch, W. Richard, Lihavainen, Heikki, Mihalopoulos, Nikolaos, Németh, Zoltán, Nie, Wei, O'Dowd, Colin, Salma, Imre, Sellegri, Karine, Svenningsson, Birgitta, Swietlicki, Erik, Tunved, Peter, Ulevicius, Vidmantas, Vakkari, Ville, Vana, Marko, Wiedensohler, Alfred, Wu, Zhijun, Virtanen, Annele, Kulmala, Markku

Atmospheric new particle formation (NPF) is an important phenomenon in terms of global particle number concentrations. Here we investigated the frequency of NPF, formation rates of 10 nm particles, and growth rates in the size range of 10–25 nm using at least 1 year of aerosol number size-distribution observations at 36 different locations around the world. The majority of these measurement sites are in the Northern Hemisphere. We found that the NPF frequency has a strong seasonal variability. At the measurement sites analyzed in this study, NPF occurs most frequently in March–May (on about 30 % of the days) and least frequently in December-February (about 10 % of the days). The median formation rate of 10 nm particles varies by about 3 orders of magnitude (0.01–10 cm−3 s−1) and the growth rate by about an order of magnitude (1–10 nm h−1). The smallest values of both formation and growth rates were observed at polar sites and the largest ones in urban environments or anthropogenically influenced rural sites. The correlation between the NPF event frequency and the particle formation and growth rate was at best moderate among the different measurement sites, as well as among the sites belonging to a certain environmental regime. For a better understanding of atmospheric NPF and its regional importance, we would need more observational data from different urban areas in practically all parts of the world, from additional remote and rural locations in North America, Asia, and most of the Southern Hemisphere (especially Australia), from polar areas, and from at least a few locations over the oceans.

2020, Filioglou, Maria, Giannakaki, Elina, Backman, John, Kesti, Jutta, Hirsikko, Anne, Engelmann, Ronny, O’Connor, Ewan, Leskinen, Jari T.T., Shang, Xiaoxia, Korhonen, Hannele, Lihavainen, Heikki, Romakkaniemi, Sami, Komppula, Mika

One year of ground-based night-time Raman lidar observations has been analysed under the Optimization of Aerosol Seeding In rain enhancement Strategies (OASIS) project, in order to characterize the aerosol particle properties over a rural site in the United Arab Emirates. In total, 1130 aerosol particle layers were detected during the 1-year measurement campaign which took place between March 2018 and February 2019. Several subsequent aerosol layers could be observed simultaneously in the atmosphere up to 11 km. The observations indicate that the measurement site is a receptor of frequent dust events, but predominantly the dust is mixed with aerosols of anthropogenic and/or marine origin. The mean aerosol optical depth over the measurement site ranged at 0.37±0.12 and 0.21±0.11 for 355 and 532 nm, respectively. Moreover, mean lidar ratios of 43±11 sr at a wavelength of 355 nm and 39±10 sr at 532 nm were found. The average linear particle depolarization ratio measured over the course of the campaign was 15±6% and 19±7% at the 355 and 532 nm wavelengths, respectively. Since the region is both a source and a receptor of mineral dust, we have also explored the properties of Arabian mineral dust of the greater area of the United Arab of Emirates and the Arabian Peninsula. The observed Arabian dust particle properties were 45±5 (42±5) sr at 355 (532) nm for the lidar ratio, 25±2% (31±2 %) for the linear particle depolarization ratio at 355 (532) nm, and 0.3±0.2 (0.2±0.2) for the extinction-related Angstrom exponent (backscatterrelated Angstrom exponent) between 355 and 532 nm. This study is the first to report comprehensive optical properties of the Arabian dust particles based on 1-year long observations, using to their fullest the capabilities of a multi-wavelength Raman lidar instrument. The results suggest that the mineral dust properties over the Middle East and western Asia, including the observation site, are comparable to those of African mineral dust with regard to the particle depolarization ratios, but not for lidar ratios. The smaller lidar ratio values in this study compared to the reference studies are attributed to the difference in the geochemical characteristics of the soil originating in the study region compared to northern Africa. © 2020 Royal Society of Chemistry. All rights reserved.

2016, Elina, Giannakaki, Pfüller, Anne, Korhonen, Kimmo, Mielonen, Tero, Laakso, Lauri, Vakkari, Ville, Baars, Holger, Engelmann, Ronny, Beukes, Johan P., Van Zyl, Pieter G., Josipovic, Miroslav, Tiitta, Petri, Chiloane, Kgaugelo, Piketh, Stuart, Lihavainen, Heikki, Lehtinen, Kari

Raman lidar data of one year was been analyzed to obtain information relating aerosol layers in the free troposphere over South Africa, Elandsfontein. In total, 375 layers were observed above the boundary layer during the period 30th January 2010 – 31st January 2011. The seasonal behavior of aerosol layer geometrical characteristics as well as intensive and extensive optical properties were studied. In general, layers were observed at higher altitudes during spring (2520 ± 970 m) while the geometrical layer depth did not show any significant seasonal dependence. The variations of most of the intensive and extensive optical properties analyzed were high during all seasons. Layers were observed at mean altitude of 2100 m ± 1000 m with lidar ratio at 355 nm of 67 ± 25 and extinction-related Ångström exponent between 355 and 532 nm of 1.9 ± 0.8.

2018, Pandolfi, Marco, Alados-Arboledas, Lucas, Alastuey, Andrés, Andrade, Marcos, Angelov, Christo, Artiñano, Begoña, Backman, John, Baltensperger, Urs, Bonasoni, Paolo, Bukowiecki, Nicolas, Collaud Coen, Martine, Conil, Sébastien, Coz, Esther, Crenn, Vincent, Dudoitis, Vadimas, Ealo, Marina, Eleftheriadis, Kostas, Favez, Olivier, Fetfatzis, Prodromos, Fiebig, Markus, Flentje, Harald, Ginot, Patrick, Gysel, Martin, Henzing, Bas, Hoffer, Andras, Holubova Smejkalova, Adela, Kalapov, Ivo, Kalivitis, Nikos, Kouvarakis, Giorgos, Kristensson, Adam, Kulmala, Markku, Lihavainen, Heikki, Lunder, Chris, Luoma, Krista, Lyamani, Hassan, Marinoni, Angela, Mihalopoulos, Nikos, Moerman, Marcel, Nicolas, José, O'Dowd, Colin, Petäjä, Tuukka, Petit, Jean-Eudes, Pichon, Jean Marc, Prokopciuk, Nina, Putaud, Jean-Philippe, Rodríguez, Sergio, Sciare, Jean, Sellegri, Karine, Swietlicki, Erik, Titos, Gloria, Tuch, Thomas, Tunved, Peter, Ulevicius, Vidmantas, Vaishya, Aditya, Vana, Milan, Virkkula, Aki, Vratolis, Stergios, Weingartner, Ernest, Wiedensohler, Alfred, Laj, Paolo

This paper presents the light-scattering properties of atmospheric aerosol particles measured over the past decade at 28 ACTRIS observatories, which are located mainly in Europe. The data include particle light scattering (σsp) and hemispheric backscattering (σbsp) coefficients, scattering Ångström exponent (SAE), backscatter fraction (BF) and asymmetry parameter (g). An increasing gradient of σsp is observed when moving from remote environments (arctic/mountain) to regional and to urban environments. At a regional level in Europe, σsp also increases when moving from Nordic and Baltic countries and from western Europe to central/eastern Europe, whereas no clear spatial gradient is observed for other station environments. The SAE does not show a clear gradient as a function of the placement of the station. However, a west-to-east-increasing gradient is observed for both regional and mountain placements, suggesting a lower fraction of fine-mode particle in western/south-western Europe compared to central and eastern Europe, where the fine-mode particles dominate the scattering. The g does not show any clear gradient by station placement or geographical location reflecting the complex relationship of this parameter with the physical properties of the aerosol particles. Both the station placement and the geographical location are important factors affecting the intraannual variability. At mountain sites, higher σsp and SAE values are measured in the summer due to the enhanced boundary layer influence and/or new particle-formation episodes. Conversely, the lower horizontal and vertical dispersion during winter leads to higher σsp values at all low-altitude sites in central and eastern Europe compared to summer. These sites also show SAE maxima in the summer (with corresponding g minima). At all sites, both SAE and g show a strong variation with aerosol particle loading. The lowest values of g are always observed together with low σsp values, indicating a larger contribution from particles in the smaller accumulation mode. During periods of high σsp values, the variation of g is less pronounced, whereas the SAE increases or decreases, suggesting changes mostly in the coarse aerosol particle mode rather than in the fine mode. Statistically significant decreasing trends of σsp are observed at 5 out of the 13 stations included in the trend analyses. The total reductions of σsp are consistent with those reported for PM2.5 and PM10 mass concentrations over similar periods across Europe.