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- ItemSimultaneous observations of a Mesospheric Inversion Layer and turbulence during the ECOMA-2010 rocket campaign(Göttingen : Copernicus, 2013) Szewczyk, A.; Strelnikov, B.; Rapp, M.; Strelnikova, I.; Baumgarten, G.; Kaifler, N.; Dunker, T.; Hoppe, U.-P.From 19 November to 19 December 2010 the fourth and final ECOMA rocket campaign was conducted at Andøya Rocket Range (69 N, 16 E) in northern Norway. We present and discuss measurement results obtained during the last rocket launch labelled ECOMA09 when simultaneous and true common volume in situ measurements of temperature and turbulence supported by ground-based lidar observations reveal two Mesospheric Inversion Layers (MIL) at heights between 71 and 73 km and between 86 and 89 km. Strong turbulence was measured in the region of the upper inversion layer, with the turbulent energy dissipation rates maximising at 2 W kg-1. This upper MIL was observed by the ALOMAR Weber Na lidar over the period of several hours. The spatial extension of this MIL as observed by the MLS instrument onboard AURA satellite was found to be more than two thousand kilometres. Our analysis suggests that both observed MILs could possibly have been produced by neutral air turbulence.
- ItemLong-term trends in the ionospheric F2 region with different solar activity indices(Göttingen : Copernicus, 2013) Mielich, J.; Bremer, J.A new comprehensive data collection by Damboldt and Suessmann (2012a) with monthly foF2 and M(3000)F2 median values is an excellent basis for the derivation of long-term trends in the ionospheric F2 region. Ionospheric trends have been derived only for stations with data series of at least 22 years (124 stations with foF2 data and 113 stations with M(3000)F2 data) using a twofold regression analysis depending on solar and geomagnetic activity. Three main results have been derived: Firstly, it could be shown that the solar 10.7 cm radio flux F10.7 is a better index for the description of the solar activity than the relative solar sunspot number R as well as the solar EUV proxy E10.7. Secondly, the global mean foF2 and
- ItemExplicit modeling of volatile organic compounds partitioning in the atmospheric aqueous phase(München : European Geopyhsical Union, 2013) Mouchel-Vallon, C.; Bräuer, P.; Camredon, M.; Valorso, R.; Madronich, S.; Hermann, M.; Aumont, B.The gas phase oxidation of organic species is a multigenerational process involving a large number of secondary compounds. Most secondary organic species are water-soluble multifunctional oxygenated molecules. The fully explicit chemical mechanism GECKO-A (Generator of Explicit Chemistry and Kinetics of Organics in the Atmosphere) is used to describe the oxidation of organics in the gas phase and their mass transfer to the aqueous phase. The oxidation of three hydrocarbons of atmospheric interest (isoprene, octane and α-pinene) is investigated for various NOx conditions. The simulated oxidative trajectories are examined in a new two dimensional space defined by the mean oxidation state and the solubility. The amount of dissolved organic matter was found to be very low (yield less than 2% on carbon atom basis) under a water content typical of deliquescent aerosols. For cloud water content, 50% (isoprene oxidation) to 70% (octane oxidation) of the carbon atoms are found in the aqueous phase after the removal of the parent hydrocarbons for low NOx conditions. For high NOx conditions, this ratio is only 5% in the isoprene oxidation case, but remains large for α-pinene and octane oxidation cases (40% and 60%, respectively). Although the model does not yet include chemical reactions in the aqueous phase, much of this dissolved organic matter should be processed in cloud drops and modify both oxidation rates and the speciation of organic species.
- ItemQuantitative determination of carbonaceous particle mixing state in Paris using single-particle mass spectrometer and aerosol mass spectrometer measurements(München : European Geopyhsical Union, 2013) Healy, R.M.; Sciare, J.; Poulain, L.; Crippa, M.; Wiedensohler, A.; Prévôt, A.S.H.; Baltensperger, U.; Sarda-Estève, R.; McGuire, M.L.; Jeong, C.-H.; McGillicuddy, E.; O'Connor, I.P.; Sodeau, J.R.; Evans, G.J.; Wenger, J.C.Single-particle mixing state information can be a powerful tool for assessing the relative impact of local and regional sources of ambient particulate matter in urban environments. However, quantitative mixing state data are challenging to obtain using single-particle mass spectrometers. In this study, the quantitative chemical composition of carbonaceous single particles has been determined using an aerosol time-of-flight mass spectrometer (ATOFMS) as part of the MEGAPOLI 2010 winter campaign in Paris, France. Relative peak areas of marker ions for elemental carbon (EC), organic aerosol (OA), ammonium, nitrate, sulfate and potassium were compared with concurrent measurements from an Aerodyne high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS), a thermal–optical OCEC analyser and a particle into liquid sampler coupled with ion chromatography (PILS-IC). ATOFMS-derived estimated mass concentrations reproduced the variability of these species well (R2 = 0.67–0.78), and 10 discrete mixing states for carbonaceous particles were identified and quantified. The chemical mixing state of HR-ToF-AMS organic aerosol factors, resolved using positive matrix factorisation, was also investigated through comparison with the ATOFMS dataset. The results indicate that hydrocarbon-like OA (HOA) detected in Paris is associated with two EC-rich mixing states which differ in their relative sulfate content, while fresh biomass burning OA (BBOA) is associated with two mixing states which differ significantly in their OA / EC ratios. Aged biomass burning OA (OOA2-BBOA) was found to be significantly internally mixed with nitrate, while secondary, oxidised OA (OOA) was associated with five particle mixing states, each exhibiting different relative secondary inorganic ion content. Externally mixed secondary organic aerosol was not observed. These findings demonstrate the range of primary and secondary organic aerosol mixing states in Paris. Examination of the temporal behaviour and chemical composition of the ATOFMS classes also enabled estimation of the relative contribution of transported emissions of each chemical species and total particle mass in the size range investigated. Only 22% of the total ATOFMS-derived particle mass was apportioned to fresh, local emissions, with 78% apportioned to regional/continental-scale emissions.
- ItemEvolution of particle composition in CLOUD nucleation experiments(München : European Geopyhsical Union, 2013) Keskinen, H.; Virtanen, A.; Joutsensaari, J.; Tsagkogeorgas, G.; Duplissy, J.; Schobesberger, S.; Gysel, M.; Riccobono, F.; Slowik, J.G.; Bianchi, F.; Yli-Juuti, T.; Lehtipalo, K.; Rondo, L.; Breitenlechner, M.; Kupc, A.; Almeida, J.; Amorim, A.; Dunne, E.M.; Downard, A.J.; Ehrhart, S.; Franchin, A.; Kajos, M.K.; Kirkby, J.; Kürten, A.; Nieminen, T.; Makhmutov, V.; Mathot, S.; Miettinen, P.; Onnela, A.; Petäjä, T.; Praplan, A.; Santos, F.D.; Schallhart, S.; Sipilä, M.; Stozhkov, Y.; Tomé, A.; Vaattovaara, P.; Wimmer, D.; Prevot, A.; Dommen, J.; Donahue, N.M.; Flagan, R.C.; Weingartner, E.; Viisanen, Y.; Riipinen, I.; Hansel, A.; Curtius, J.; Kulmala, M.; Worsnop, D.R.; Baltensperger, U.; Wex, H.; Stratmann, F.; Laaksonen, A.Sulphuric acid, ammonia, amines, and oxidised organics play a crucial role in nanoparticle formation in the atmosphere. In this study, we investigate the composition of nucleated nanoparticles formed from these compounds in the CLOUD (Cosmics Leaving Outdoor Droplets) chamber experiments at CERN (Centre européen pour la recherche nucléaire). The investigation was carried out via analysis of the particle hygroscopicity, ethanol affinity, oxidation state, and ion composition. Hygroscopicity was studied by a hygroscopic tandem differential mobility analyser and a cloud condensation nuclei counter, ethanol affinity by an organic differential mobility analyser and particle oxidation level by a high-resolution time-of-flight aerosol mass spectrometer. The ion composition was studied by an atmospheric pressure interface time-of-flight mass spectrometer. The volume fraction of the organics in the particles during their growth from sizes of a few nanometers to tens of nanometers was derived from measured hygroscopicity assuming the Zdanovskii–Stokes–Robinson relationship, and compared to values gained from the spectrometers. The ZSR-relationship was also applied to obtain the measured ethanol affinities during the particle growth, which were used to derive the volume fractions of sulphuric acid and the other inorganics (e.g. ammonium salts). In the presence of sulphuric acid and ammonia, particles with a mobility diameter of 150 nm were chemically neutralised to ammonium sulphate. In the presence of oxidation products of pinanediol, the organic volume fraction of freshly nucleated particles increased from 0.4 to ~0.9, with an increase in diameter from 2 to 63 nm. Conversely, the sulphuric acid volume fraction decreased from 0.6 to 0.1 when the particle diameter increased from 2 to 50 nm. The results provide information on the composition of nucleated aerosol particles during their growth in the presence of various combinations of sulphuric acid, ammonia, dimethylamine and organic oxidation products.
- ItemPrimary and secondary organic aerosol origin by combined gas-particle phase source apportionment(München : European Geopyhsical Union, 2013) Crippa, M.; Canonaco, F.; Slowik, J.G.; El Haddad, I.; DeCarlo, P.F.; Mohr, C.; Heringa, M.F.; Chirico, R.; Marchand, N.; Temime-Roussel, B.; Abidi, E.; Poulain, L.; Wiedensohler, A.; Baltensperger, U.; Prévôt, A.S.H.Secondary organic aerosol (SOA), a prominent fraction of particulate organic mass (OA), remains poorly constrained. Its formation involves several unknown precursors, formation and evolution pathways and multiple natural and anthropogenic sources. Here a combined gas-particle phase source apportionment is applied to wintertime and summertime data collected in the megacity of Paris in order to investigate SOA origin during both seasons. This was possible by combining the information provided by an aerosol mass spectrometer (AMS) and a proton transfer reaction mass spectrometer (PTR-MS). A better constrained apportionment of primary OA (POA) sources is also achieved using this methodology, making use of gas-phase tracers. These tracers made possible the discrimination between biogenic and continental/anthropogenic sources of SOA. We found that continental SOA was dominant during both seasons (24–50% of total OA), while contributions from photochemistry-driven SOA (9% of total OA) and marine emissions (13% of total OA) were also observed during summertime. A semi-volatile nighttime component was also identified (up to 18% of total OA during wintertime). This approach was successfully applied here and implemented in a new source apportionment toolkit.
- ItemOptimizing CALIPSO Saharan dust retrievals(München : European Geopyhsical Union, 2013) Amiridis, V.; Wandinger, U.; Marinou, E.; Giannakaki, E.; Tsekeri, A.; Basart, S.; Kazadzis, S.; Gkikas, A.; Taylor, M.; Baldasano, J.; Ansmann, A.We demonstrate improvements in CALIPSO (Cloud–Aerosol Lidar and Infrared Pathfinder Satellite Observations) dust extinction retrievals over northern Africa and Europe when corrections are applied regarding the Saharan dust lidar ratio assumption, the separation of the dust portion in detected dust mixtures, and the averaging scheme introduced in the Level 3 CALIPSO product. First, a universal, spatially constant lidar ratio of 58 sr instead of 40 sr is applied to individual Level 2 dust-related backscatter products. The resulting aerosol optical depths show an improvement compared with synchronous and collocated AERONET (Aerosol Robotic Network) measurements. An absolute bias of the order of −0.03 has been found, improving on the statistically significant biases of the order of −0.10 reported in the literature for the original CALIPSO product. When compared with the MODIS (Moderate-Resolution Imaging Spectroradiometer) collocated aerosol optical depth (AOD) product, the CALIPSO negative bias is even less for the lidar ratio of 58 sr. After introducing the new lidar ratio for the domain studied, we examine potential improvements to the climatological CALIPSO Level 3 extinction product: (1) by introducing a new methodology for the calculation of pure dust extinction from dust mixtures and (2) by applying an averaging scheme that includes zero extinction values for the nondust aerosol types detected. The scheme is applied at a horizontal spatial resolution of 1° × 1° for ease of comparison with the instantaneous and collocated dust extinction profiles simulated by the BSC-DREAM8b dust model. Comparisons show that the extinction profiles retrieved with the proposed methodology reproduce the well-known model biases per subregion examined. The very good agreement of the proposed CALIPSO extinction product with respect to AERONET, MODIS and the BSC-DREAM8b dust model makes this dataset an ideal candidate for the provision of an accurate and robust multiyear dust climatology over northern Africa and Europe.
- ItemGlyoxal and methylglyoxal in Atlantic seawater and marine aerosol particles: Method development and first application during the polarstern cruise ANT XXVII/4(München : European Geopyhsical Union, 2013) van Pinxteren, M.; Herrmann, H.An analytical method for the determination of the alpha dicarbonyls glyoxal (GLY) and methylglyoxal (MGLY) from seawater and marine aerosol particles is presented. The method is based on derivatization with o-(2,3,4,5,6-Pentafluorobenzyl)-hydroxylamine (PFBHA) reagent, solvent extraction and GC-MS (SIM) analysis. The method showed good precision (RSD < 10%), sensitivity (detection limits in the low ng L−1 range), and accuracy (good agreement between external calibration and standard addition). The method was applied to determine GLY and MGLY in oceanic water sampled during the Polarstern cruise ANT XXVII/4 from Capetown to Bremerhaven in spring 2011. GLY and MGLY were determined in the sea surface microlayer (SML) of the ocean and corresponding bulk water (BW) with average concentrations of 228 ng L−1 (GLY) and 196 ng L−1 (MGLY). The results show a significant enrichment (factor of 4) of GLY and MGLY in the SML. Furthermore, marine aerosol particles (PM1) were sampled during the cruise and analyzed for GLY (average concentration 0.19 ng m−3) and MGLY (average concentration 0.15 ng m−3). On aerosol particles, both carbonyls show a very good correlation with oxalate, supporting the idea of a secondary formation of oxalic acid via GLY and MGLY. Concentrations of GLY and MGLY in seawater and on aerosol particles were correlated to environmental parameters such as global radiation, temperature, distance to the coastline and biological activity. There are slight hints for a photochemical production of GLY and MGLY in the SML (significant enrichment in the SML, higher enrichment at higher temperature). However, a clear connection of GLY and MGLY to global radiation as well as to biological activity cannot be concluded from the data. A slight correlation between GLY and MGLY in the SML and in aerosol particles could be a hint for interactions, in particular of GLY, between seawater and the atmosphere.
- ItemComparing two years of Saharan dust source activation obtained by regional modelling and satellite observations(München : European Geopyhsical Union, 2013) Tegen, I.; Schepanski, K.; Heinold, B.A regional-scale dust model is used to simulate Saharan dust emissions and atmospheric distributions in the years 2007 and 2008. The model results are compared to dust source activation events compiled from infrared dust index imagery from the geostationary Meteosat Second Generation (MSG) satellite. The observed morning maximum in dust source activation frequencies indicates that the breakdown of nocturnal low level jets is an important mechanism for dust source activation in the Sahara. The comparison shows that the time of the day of the onset of dust emission is delayed in the model compared to the observations. Also, the simulated number of dust emission events associated with nocturnal low level jets in mountainous regions is underestimated in the model. The MSG dust index observations indicate a strong increase in dust source activation frequencies in the year 2008 compared to 2007. The difference between the two years is less pronounced in the model. Observations of dust optical thickness, e.g. at stations of the sunphotometer network AERONET, do not show such increase, in agreement with the model results. This indicates that the number of observed dust activation events is only of limited use for estimating actual dust emission fluxes in the Sahara. The ability to reproduce interannual variability of Saharan dust with models remains an important challenge for understanding the controls of the atmospheric dust load.
- ItemAerosol particle measurements at three stationary sites in the megacity of Paris during summer 2009: Meteorology and air mass origin dominate aerosol particle composition and size distribution(München : European Geopyhsical Union, 2013) Freutel, F.; Schneider, J.; Drewnick, F.; Weiden-Reinmüller, S.-L.; Crippa, M.; Prévôt, A.S.H.; Baltensperger, U.; Poulain, L.; Wiedensohler, R.A.; Sciare, J.; Sarda-Estève, R.; Burkhart, J.F.; Eckhardt, S.; Stohl, A.; Gros, V.; Colomb, A.; Michoud, V.; Doussin, J.F.; Borbon, A.; Haeffelin, M.; Morille, Y.; Beekmann, M.; Borrmann, S.During July 2009, a one-month measurement campaign was performed in the megacity of Paris. Amongst other measurement platforms, three stationary sites distributed over an area of 40 km in diameter in the greater Paris region enabled a detailed characterization of the aerosol particle and gas phase. Simulation results from the FLEXPART dispersion model were used to distinguish between different types of air masses sampled. It was found that the origin of air masses had a large influence on measured mass concentrations of the secondary species particulate sulphate, nitrate, ammonium, and oxygenated organic aerosol measured with the Aerodyne aerosol mass spectrometer in the submicron particle size range: particularly high concentrations of these species (about 4 μg m−3, 2 μg m−3, 2 μg m−3, and 7 μg m−3, respectively) were measured when aged material was advected from continental Europe, while for air masses originating from the Atlantic, much lower mass concentrations of these species were observed (about 1 μg m−3, 0.2 μg m−3, 0.4 μg m−3, and 1–3 μg m−3, respectively). For the primary emission tracers hydrocarbon-like organic aerosol, black carbon, and NOx it was found that apart from diurnal source strength variations and proximity to emission sources, local meteorology had the largest influence on measured concentrations, with higher wind speeds leading to larger dilution and therefore smaller measured concentrations. Also the shape of particle size distributions was affected by wind speed and air mass origin. Quasi-Lagrangian measurements performed under connected flow conditions between the three stationary sites were used to estimate the influence of the Paris emission plume onto its surroundings, which was found to be rather small. Rough estimates for the impact of the Paris emission plume on the suburban areas can be inferred from these measurements: Volume mixing ratios of 1–14 ppb of NOx, and upper limits for mass concentrations of about 1.5 μg m−3 of black carbon and of about 3 μg m−3 of hydrocarbon-like organic aerosol can be deduced which originate from both, local emissions and the overall Paris emission plume. The secondary aerosol particle phase species were found to be not significantly influenced by the Paris megacity, indicating their regional origin. The submicron aerosol mass concentrations of particulate sulphate, nitrate, and ammonium measured during time periods when air masses were advected from eastern central Europe were found to be similar to what has been found from other measurement campaigns in Paris and south-central France for this type of air mass origin, indicating that the results presented here are also more generally valid.