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Author: Baltensperger, U. × Author: Wiedensohler, A. × End date: 2019 × Start date: 2010 × Type: Article × Subject: air quality × Subject: concentration (composition) ×

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    Recommendations for reporting "black carbon" measurements
    (München : European Geopyhsical Union, 2013) Petzold, A.; Ogren, J.A.; Fiebig, M.; Laj, P.; Li, S.-M.; Baltensperger, U.; Holzer-Popp, T.; Kinne, S.; Pappalardo, G.; Sugimoto, N.; Wehrli, C.; Wiedensohler, A.; Zhang, X.-Y.
    Although black carbon (BC) is one of the key atmospheric particulate components driving climate change and air quality, there is no agreement on the terminology that considers all aspects of specific properties, definitions, measurement methods, and related uncertainties. As a result, there is much ambiguity in the scientific literature of measurements and numerical models that refer to BC with different names and based on different properties of the particles, with no clear definition of the terms. The authors present here a recommended terminology to clarify the terms used for BC in atmospheric research, with the goal of establishing unambiguous links between terms, targeted material properties and associated measurement techniques.
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    A synthesis of cloud condensation nuclei counter (CCNC) measurements within the EUCAARI network
    (München : European Geopyhsical Union, 2015) Paramonov, M.; Kerminen, V.-M.; Gysel, M.; Aalto, P.P.; Andreae, M.O.; Asmi, E.; Baltensperger, U.; Bougiatioti, A.; Brus, D.; Frank, G.P.; Good, N.; Gunthe, S.S.; Hao, L.; Irwin, M.; Jaatinen, A.; Jurányi, Z.; King, S.M.; Kortelainen, A.; Kristensson, A.; Lihavainen, H.; Kulmala, M.; Lohmann, U.; Martin, S.T.; McFiggans, G.; Mihalopoulos, N.; Nenes, A.; O'Dowd, C.D.; Ovadnevaite, J.; Petäjä, T.; Pöschl, U.; Roberts, G.C.; Rose, D.; Svenningsson, B.; Swietlicki, E.; Weingartner, E.; Whitehead, J.; Wiedensohler, A.; Wittbom, C.; Sierau, B.
    Cloud condensation nuclei counter (CCNC) measurements performed at 14 locations around the world within the European Integrated project on Aerosol Cloud Climate and Air Quality interactions (EUCAARI) framework have been analysed and discussed with respect to the cloud condensation nuclei (CCN) activation and hygroscopic properties of the atmospheric aerosol. The annual mean ratio of activated cloud condensation nuclei (NCCN) to the total number concentration of particles (NCN), known as the activated fraction A, shows a similar functional dependence on supersaturation S at many locations – exceptions to this being certain marine locations, a free troposphere site and background sites in south-west Germany and northern Finland. The use of total number concentration of particles above 50 and 100 nm diameter when calculating the activated fractions (A50 and A100, respectively) renders a much more stable dependence of A on S; A50 and A100 also reveal the effect of the size distribution on CCN activation. With respect to chemical composition, it was found that the hygroscopicity of aerosol particles as a function of size differs among locations. The hygroscopicity parameter κ decreased with an increasing size at a continental site in south-west Germany and fluctuated without any particular size dependence across the observed size range in the remote tropical North Atlantic and rural central Hungary. At all other locations κ increased with size. In fact, in Hyytiälä, Vavihill, Jungfraujoch and Pallas the difference in hygroscopicity between Aitken and accumulation mode aerosol was statistically significant at the 5 % significance level. In a boreal environment the assumption of a size-independent κ can lead to a potentially substantial overestimation of NCCN at S levels above 0.6 %. The same is true for other locations where κ was found to increase with size. While detailed information about aerosol hygroscopicity can significantly improve the prediction of NCCN, total aerosol number concentration and aerosol size distribution remain more important parameters. The seasonal and diurnal patterns of CCN activation and hygroscopic properties vary among three long-term locations, highlighting the spatial and temporal variability of potential aerosol–cloud interactions in various environments.