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- ItemEUCAARI ion spectrometer measurements at 12 European sites – analysis of new particle formation events(München : European Geopyhsical Union, 2010) Manninen, H.E.; Nieminen, T.; Asmi, E.; Gagné, S.; Häkkinen, S.; Lehtipalo, K.; Aalto, P.; Vana, M.; Mirme, A.; Mirme, S.; Hõrrak, U.; Plass-Dülmer, C.; Stange, G.; Kiss, G.; Hoffer, A.; Törő, N.; Moerman, M.; Henzing, B.; de Leeuw, G.; Brinkenberg, M.; Kouvarakis, G.N.; Bougiatioti, A.; Mihalopoulos, N.; O'Dowd, C.; Ceburnis, D.; Arneth, A.; Svenningsson, B.; Swietlicki, E.; Tarozzi, L.; Decesari, S.; Facchini, M.C.; Birmili, W.; Sonntag, A.; Wiedensohler, A.; Boulon, J.; Sellegri, K.; Laj, P.; Gysel, M.; Bukowiecki, N.; Weingartner, E.; Wehrle, G.; Laaksonen, A.; Hamed, A.; Joutsensaari, J.; Petäjä, T.; Kerminen, V.-M.; Kulmala, M.We present comprehensive results on continuous atmospheric cluster and particle measurements in the size range ~1–42 nm within the European Integrated project on Aerosol Cloud Climate and Air Quality interactions (EUCAARI) project. We focused on characterizing the spatial and temporal variation of new particle formation events and relevant particle formation parameters across Europe. Different types of air ion and cluster mobility spectrometers were deployed at 12 field sites across Europe from March 2008 to May 2009. The measurements were conducted in a wide variety of environments, including coastal and continental locations as well as sites at different altitudes (both in the boundary layer and the free troposphere). New particle formation events were detected at all of the 12 field sites during the year-long measurement period. From the data, nucleation and growth rates of newly formed particles were determined for each environment. In a case of parallel ion and neutral cluster measurements, we could also estimate the relative contribution of ion-induced and neutral nucleation to the total particle formation. The formation rates of charged particles at 2 nm accounted for 1–30% of the corresponding total particle formation rates. As a significant new result, we found out that the total particle formation rate varied much more between the different sites than the formation rate of charged particles. This work presents, so far, the most comprehensive effort to experimentally characterize nucleation and growth of atmospheric molecular clusters and nanoparticles at ground-based observation sites on a continental scale.
- ItemA European aerosol phenomenology - 7: High-time resolution chemical characteristics of submicron particulate matter across Europe(Amsterdam : Elsevier, 2021) Bressi, M.; Cavalli, F.; Putaud, J.P.; Fröhlich, R.; Petit, J.-E.; Aas, W.; Äijälä, M.; Alastuey, A.; Allan, J.D.; Aurela, M.; Berico, M.; Bougiatioti, A.; Bukowiecki, N.; Canonaco, F.; Crenn, V.; Dusanter, S.; Ehn, M.; Elsasser, M.; Flentje, H.; Graf, P.; Green, D.C.; Heikkinen, L.; Hermann, H.; Holzinger, R.; Hueglin, C.; Keernik, H.; Kiendler-Scharr, A.; Kubelová, L.; Lunder, C.; Maasikmets, M.; Makeš, O.; Malaguti, A.; Mihalopoulos, N.; Nicolas, J.B.; O'Dowd, C.; Ovadnevaite, J.; Petralia, E.; Poulain, L.; Priestman, M.; Riffault, V.; Ripoll, A.; Schlag, P.; Schwarz, J.; Sciare, J.; Slowik, J.; Sosedova, Y.; Stavroulas, I.; Teinemaa, E.; Via, M.; Vodička, P.; Williams, P.I.; Wiedensohler, A.; Young, D.E.; Zhang, S.; Favez, O.; Minguillón, M.C.; Prevot, A.S.H.Similarities and differences in the submicron atmospheric aerosol chemical composition are analyzed from a unique set of measurements performed at 21 sites across Europe for at least one year. These sites are located between 35 and 62°N and 10° W – 26°E, and represent various types of settings (remote, coastal, rural, industrial, urban). Measurements were all carried out on-line with a 30-min time resolution using mass spectroscopy based instruments known as Aerosol Chemical Speciation Monitors (ACSM) and Aerosol Mass Spectrometers (AMS) and following common measurement guidelines. Data regarding organics, sulfate, nitrate and ammonium concentrations, as well as the sum of them called non-refractory submicron aerosol mass concentration ([NR-PM1]) are discussed. NR-PM1 concentrations generally increase from remote to urban sites. They are mostly larger in the mid-latitude band than in southern and northern Europe. On average, organics account for the major part (36–64%) of NR-PM1 followed by sulfate (12–44%) and nitrate (6–35%). The annual mean chemical composition of NR-PM1 at rural (or regional background) sites and urban background sites are very similar. Considering rural and regional background sites only, nitrate contribution is higher and sulfate contribution is lower in mid-latitude Europe compared to northern and southern Europe. Large seasonal variations in concentrations (μg/m³) of one or more components of NR-PM1 can be observed at all sites, as well as in the chemical composition of NR-PM1 (%) at most sites. Significant diel cycles in the contribution to [NR-PM1] of organics, sulfate, and nitrate can be observed at a majority of sites both in winter and summer. Early morning minima in organics in concomitance with maxima in nitrate are common features at regional and urban background sites. Daily variations are much smaller at a number of coastal and rural sites. Looking at NR-PM1 chemical composition as a function of NR-PM1 mass concentration reveals that although organics account for the major fraction of NR-PM1 at all concentration levels at most sites, nitrate contribution generally increases with NR-PM1 mass concentration and predominates when NR-PM1 mass concentrations exceed 40 μg/m³ at half of the sites. © 2021 The Authors
- ItemInstrumentation and Measurement Strategy for the NOAA SENEX Aircraft Campaign as Part of the Southeast Atmosphere Study 2013(Katlenburg-Lindau : Copernicus, 2016) Warneke, C.; Trainer, M.; de Gouw, J.A.; Parrish, D.D.; Fahey, D.W.; Ravishankara, A.R.; Middlebrook, A.M.; Brock, C.A.; Roberts, J.M.; Brown, S.S.; Neuman, J.A.; Lerner, B.M.; Lack, D.; Law, D.; Hübler, G.; Pollack, I.; Sjostedt, S.; Ryerson, T.B.; Gilman, J B; Liao, J.; Holloway, J.; Peischl, J.; Nowak, J.B.; Aikin, K.; Min, K.-E.; Washenfelder, R.A.; Graus, M.G.; Richardson, M.; Markovic, M.Z.; Wagner, N.L.; Welti, A.; Veres, P.R.; Edwards, P.; Schwarz, J.P.; Gordon, T.; Dube, W.P.; McKeen, S.; Brioude, J.; Ahmadov, R.; Bougiatioti, A.; Lin, J.J.; Nenes, A.; Wolfe, G.M.; Hanisco, T.F.; Lee, B.H.; Lopez-Hilfiker, F.D.; Thornton, J.A.; Keutsch, F.N.; Kaiser, J.; Mao, J.; Hatch, C.Natural emissions of ozone-and-aerosol-precursor gases such as isoprene and monoterpenes are high in the southeast of the US. In addition, anthropogenic emissions are significant in the Southeast US and summertime photochemistry is rapid. The NOAA-led SENEX (Southeast Nexus) aircraft campaign was one of the major components of the Southeast Atmosphere Study (SAS) and was focused on studying the interactions between biogenic and anthropogenic emissions to form secondary pollutants. During SENEX, the NOAA WP-3D aircraft conducted 20 research flights between 27 May and 10 July 2013 based out of Smyrna, TN. Here we describe the experimental approach, the science goals and early results of the NOAA SENEX campaign. The aircraft, its capabilities and standard measurements are described. The instrument payload is summarized including detection limits, accuracy, precision and time resolutions for all gas-and-aerosol phase instruments. The inter-comparisons of compounds measured with multiple instruments on the NOAA WP-3D are presented and were all within the stated uncertainties, except two of the three NO2 measurements. The SENEX flights included day- and nighttime flights in the Southeast as well as flights over areas with intense shale gas extraction (Marcellus, Fayetteville and Haynesville shale). We present one example flight on 16 June 2013, which was a daytime flight over the Atlanta region, where several crosswind transects of plumes from the city and nearby point sources, such as power plants, paper mills and landfills, were flown. The area around Atlanta has large biogenic isoprene emissions, which provided an excellent case for studying the interactions between biogenic and anthropogenic emissions. In this example flight, chemistry in and outside the Atlanta plumes was observed for several hours after emission. The analysis of this flight showcases the strategies implemented to answer some of the main SENEX science questions.
- ItemA 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.