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A global analysis of climate-relevant aerosol properties retrieved from the network of Global Atmosphere Watch (GAW) near-surface observatories
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.
Long-term cloud condensation nuclei number concentration, particle number size distribution and chemical composition measurements at regionally representative observatories
2018, Schmale, Julia, Henning, Silvia, Decesari, Stefano, Henzing, Bas, Keskinen, Helmi, Sellegri, Karine, Ovadnevaite, Jurgita, Pöhlker, Mira L., Brito, Joel, Bougiatioti, Aikaterini, Kristensson, Adam, Kalivitis, Nikos, Stavroulas, Iasonas, Carbone, Samara, Jefferson, Anne, Park, Minsu, Schlag, Patrick, Iwamoto, Yoko, Aalto, Pasi, Äijälä, Mikko, Bukowiecki, Nicolas, Ehn, Mikael, Frank, Göran, Fröhlich, Roman, Frumau, Arnoud, Herrmann, Erik, Herrmann, Hartmut, Holzinger, Rupert, Kos, Gerard, Kulmala, Markku, Mihalopoulos, Nikolaos, Nenes, Athanasios, O'Dowd, Colin, Petäjä, Tuukka, Picard, David, Pöhlker, Christopher, Pöschl, Ulrich, Poulain, Laurent, Prévôt, André Stephan Henry, Swietlicki, Erik, Andreae, Meinrat O., Artaxo, Paulo, Wiedensohler, Alfred, Ogren, John, Matsuki, Atsushi, Yum, Seong Soo, Stratmann, Frank, Baltensperger, Urs, Gysel, Martin
Aerosol-cloud interactions (ACI) constitute the single largest uncertainty in anthropogenic radiative forcing. To reduce the uncertainties and gain more confidence in the simulation of ACI, models need to be evaluated against observations, in particular against measurements of cloud condensation nuclei (CCN). Here we present a data set - ready to be used for model validation - of long-term observations of CCN number concentrations, particle number size distributions and chemical composition from 12 sites on 3 continents. Studied environments include coastal background, rural background, alpine sites, remote forests and an urban surrounding. Expectedly, CCN characteristics are highly variable across site categories. However, they also vary within them, most strongly in the coastal background group, where CCN number concentrations can vary by up to a factor of 30 within one season. In terms of particle activation behaviour, most continental stations exhibit very similar activation ratios (relative to particles 20nm) across the range of 0.1 to 1.0% supersaturation. At the coastal sites the transition from particles being CCN inactive to becoming CCN active occurs over a wider range of the supersaturation spectrum. Several stations show strong seasonal cycles of CCN number concentrations and particle number size distributions, e.g. at Barrow (Arctic haze in spring), at the alpine stations (stronger influence of polluted boundary layer air masses in summer), the rain forest (wet and dry season) or Finokalia (wildfire influence in autumn). The rural background and urban sites exhibit relatively little variability throughout the year, while short-term variability can be high especially at the urban site. The average hygroscopicity parameter, calculated from the chemical composition of submicron particles was highest at the coastal site of Mace Head (0.6) and lowest at the rain forest station ATTO (0.2-0.3). We performed closure studies based on -Köhler theory to predict CCN number concentrations. The ratio of predicted to measured CCN concentrations is between 0.87 and 1.4 for five different types of . The temporal variability is also well captured, with Pearson correlation coefficients exceeding 0.87. Information on CCN number concentrations at many locations is important to better characterise ACI and their radiative forcing. But long-term comprehensive aerosol particle characterisations are labour intensive and costly. Hence, we recommend operating migrating-CCNCs to conduct collocated CCN number concentration and particle number size distribution measurements at individual locations throughout one year at least to derive a seasonally resolved hygroscopicity parameter. This way, CCN number concentrations can only be calculated based on continued particle number size distribution information and greater spatial coverage of long-term measurements can be achieved.
Occurrence of an ultrafine particle mode less than 20 nm in diameter in the marine boundary layer during Arctic summer and autumn
2017, Wiedensohler, Alfred, Covert, David S., Swietlicki, Erik, Aalto, Pasi, Heintzenberg, Jost, Leck, Caroline
The International Arctic Ocean Expedition 1991 (IAOE-91) provided a platform to study the occurrence and size distributions of ultrafine particles in the marine boundary layer (MBL) during Arctic summer and autumn. Measurements of both aerosol physics, and gas/particulate chemistry were taken aboard the Swedish icebreaker Oden. Three separate submicron aerosol modes were found: an ultrafine mode (Dp < 20 nm), the Aitken mode (20 < Dp < 100 nm), and the accumulation mode (Dp > 100 nm). We evaluated correlations between ultrafine particle number concentrations and mean diameter with the entire measured physical, chemical, and meteorological data set. Multivariate statistical methods were then used to make these comparisons. A principal component (PC) analysis indicated that the observed variation in the data could be explained by the influence from several types of air masses. These were characterised by contributions from the open sea or sources from the surrounding continents and islands. A partial least square (PLS) regression of the ultrafine particle concentration was also used. These results implied that the ultrafine particles were produced above or in upper layers of the MBL and mixed downwards. There were also indications that the open sea acted as a source of the precursors for ultrafine particle production. No anti-correlation was found between the ultrafine and accumulation particle number concentrations, thus indicating that the sources were in separate air masses.