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search.filters.applied.f.access: openAccess × Author: Wiedensohler, Alfred × Publisher: Milton Park : Taylor & Francis × Subject: size distribution ×

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Now showing 1 - 6 of 6
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    Cloud condensation nuclei spectra derived from size distributions and hygroscopic properties of the aerosol in coastal south-west Portugal during ACE-2
    (Milton Park : Taylor & Francis, 2016) Dusek, Ulrike; Covert, David S.; Wiedensohler, Alfred; Neusüss, Christian; Weise, Diana; Cantrell, Will
    In this work we propose and test a method to calculate cloud condensation nuclei (CCN) spectra basedon aerosol number size distributions and hygroscopic growth factors. Sensitivity studies show thatthis method can be used in a wide variety of conditions except when the aerosol consist mainly oforganic compounds. One crucial step in the calculations, estimating soluble ions in an aerosol particlebased on hygroscopic growth factors, is tested in an internal hygroscopic consistency study. The resultsshow that during the second Aerosol Characterization Experiment (ACE-2) the number concentrationof inorganic ions analyzed in impactor samples could be reproduced from measured growth factorswithin the measurement uncertainties at the measurement site in Sagres, Portugal. CCN spectra were calculated based on data from the ACE-2 field experiment at the Sagres site.The calculations overestimate measured CCN spectra on average by approximately 30%, which iscomparable to the uncertainties in measurements and calculations at supersaturations below 0.5%. Thecalculated CCN spectra were averaged over time periods when Sagres received clean air masses and airmasses influenced by aged and recent pollution. Pollution outbreaks enhance the CCN concentrationsat supersaturations near 0.2% by a factor of 3 (aged pollution) to 5 (recent pollution) compared to theclean marine background concentrations. In polluted air masses, the shape of the CCN spectra changes.The clean spectra can be approximated by a power function, whereas the polluted spectra are betterapproximated by an error function.
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    In situ aerosol characterization at Cape Verde, Part 1: Particle number size distributions, hygroscopic growth and state of mixing of the marine and Saharan dust aerosol
    (Milton Park : Taylor & Francis, 2017) Schladitz, Alexander; Müller, Thomas; Nowak, Andreas; Kandler, Konrad; Lieke, Kirsten; Massling, Andreas; Wiedensohler, Alfred
    Particle number size distributions and hygroscopic properties of marine and Saharan dust aerosol were investigated during the SAMUM-2 field study at Cape Verde in winter 2008. Aitken and accumulation mode particles were mainly assigned to the marine aerosol, whereas coarse mode particles were composed of sea-salt and a variable fraction of Saharan mineral dust. A new methodical approach was used to derive hygroscopic growth and state of mixing for a particle size range (volume equivalent) from dpve = 26 nm to 10 μm. For hygroscopic particles with dpve < 100 nm, the median hygroscopicity parameter κ is 0.35. From 100 nm < dpve < 350 nm, κ increases to 0.65. For larger particles, κ at dpve = 350 nm was used. For nearly hydrophobic particles, κ is between 0 and 0.1 for dpve < 250 nm and decreases to 0 for dpve > 250 nm. The mixing state of Saharan dust in terms of the number fraction of nearly hydrophobic particles showed the highest variation and ranges from 0.3 to almost 1. This study was used to perform a successful mass closure at ambient conditions and demonstrates the important role of hygroscopic growth of large sea-salt particles.
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    Regional Saharan dust modelling during the SAMUM 2006 campaign
    (Milton Park : Taylor & Francis, 2017) Heinold, Bernd; Tegen, Ina; Esselborn, Michael; Kandler, Konrad; Knippertz, Peter; Müller, Detlef; Schladitz, Alexander; Tesche, Matthias; Weinzierl, Bernadett; Ansmann, Albert; Althausen, Dietrich; Laurent, Benoit; Massling, Andreas; Müller, Thomas; Petzold, Andreas; Schepanski, Kerstin; Wiedensohler, Alfred
    The regional dust model system LM-MUSCAT-DES was developed in the framework of the SAMUM project. Using the unique comprehensive data set of near-source dust properties during the 2006SAMUMfield campaign, the performance of the model system is evaluated for two time periods in May and June 2006. Dust optical thicknesses, number size distributions and the position of the maximum dust extinction in the vertical profiles agree well with the observations. However, the spatio-temporal evolution of the dust plumes is not always reproduced due to inaccuracies in the dust source placement by the model. While simulated winds and dust distributions are well matched for dust events caused by dry synoptic-scale dynamics, they are often misrepresented when dust emissions are caused by moist convection or influenced by small-scale topography that is not resolved by the model. In contrast to long-range dust transport, in the vicinity of source regions the model performance strongly depends on the correct prediction of the exact location of sources. Insufficiently resolved vertical grid spacing causes the absence of inversions in the model vertical profiles and likely explains the absence of the observed sharply defined dust layers.
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    Structure, variability and persistence of the submicrometre marine aerosol
    (Milton Park : Taylor & Francis, 2017) Heintzenberg, Jost; Birmili, Wolfram; Wiedensohler, Alfred; Nowak, Andreas; Tuch, Thomas
    Submicrometre dry number size distributions from four marine and one continental aerosol experiment were evaluatedjointly in the present study. In the marine experiments only data with back trajectories of at least 120 h without landcontact were used to minimize continental contamination. Log-normal functions were fitted to the size distributions.Basic statistics of the marine aerosol indicate a closed character of the size distribution at the lower size limit as opposedto an open character for corresponding continental data. Together with the infrequent occurrences of marine particlesbelow20 nmthis finding supports hypotheses and model results suggesting lowprobabilities of homogeneous nucleationin the marine boundary layer. The variability of submicrometre marine number concentrations was parametrized witha bimodal log-normal function that quantifies the probability of finding different number concentrations about a givenmedian value. Together with a four-modal log-normal approximation of the submicrometre marine size distributionitself, this model allows a statistical representation of the marine aerosol that facilitates comparison of experiments andvalidation of aerosol models. Autocorrelation at the one fixed marine site with a minimum of interruptions in timesseriesrevealed a strong size dependency of persistence in particle number concentration with the shortest persistenceat the smallest sizes. Interestingly, in the marine aerosol (at Cape Grim) persistence exhibits a size dependency thatlargely matches the modes in dg0, i.e. near the most frequent geometric mean diameters number concentrations aremost persistent. Over the continent, persistence of particle numbers is strongly constrained by diurnal meteorologicalprocesses and aerosol dynamics. Thus, no strong modal structure appears in the size-dependent persistence at Melpitz.As with the aerosol variability, marine aerosol processes in models of aerosol dynamics can be tested with these findings.
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    Aerosol number to volume ratios in Southwest Portugal during ACE-2
    (Milton Park : Taylor & Francis, 2017) Dusek, Ulrike; Covert, David S.; Wiedensohler, Alfred; Neusúss, Christian; Weise, Diana
    Past studies have indicated that long-term averages of the aerosol number to volume ratios (defined as the number of particles larger than a certain diameter divided by the particle volume over some range less than 1 μm) show little variability over the Atlantic. This work presents number to volume ratios (R) measured during the ACE-2 experiment on the land-based Sagres field site located in Southwest Portugal. The values of R measured in Sagres compare reasonably well with previous measurements over the Atlantic. The main emphasis of this work is therefore to investigate more closely possible reasons for the observed stability of the number to volume ratio. Aerosol number size distributions measured in Sagres are parametrized by the sum of two log-normal distributions fitted to the accumulation and to the Aitken mode. The main factor that limits the variability of R is that the parameters of these log-normal distributions are not always independent but show some covariance. In polluted air mass types correlations between parameters of the Aitken and accumulation mode are mostly responsible for stabilizing R. In marine air mass types the variability of R is reduced by an inverse relationship between the accumulation-mode mean diameter and standard deviation, consistent with condensational processes and cloud processing working on the aerosol. However, despite this reduction, the variability of R in marine air mass types is still considerable and R is linearly dependent on the number concentration of particles larger than 90 nm. This partly due to a mil of Aitken-mode particles extending to sizes larger than 90 nm.
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    Aerosol number-size distributions during clear and fog periods in the summer high Arctic: 1991, 1996 and 2001
    (Milton Park : Taylor & Francis, 2017) Heintzenberg, Jost; Leck, Caroline; Birmili, Wolfram; Wehner, Birgit; Tjernström, Michael; Wiedensohler, Alfred
    The present study covers submicrometer aerosol size distribution data taken during three Arctic icebreaker expeditions in the summers of 1991, 1996 and 2001. The size distributions of all expeditions were compared in log-normally fitted form to the statistics of the marine number size distribution provided by Heintzenberg et al. (2004) yielding rather similar log-normal parameters of the modes. Statistics of the modal concentrations revealed strong concentration decreases of large accumulation mode particles with increasing length of time spent over the pack ice. The travel-time dependencies of both Aitken and ultrafine modes strongly indicate, as other studies did before, the occurrence of fine-particle sources in the inner Arctic. With two approaches evidence of fog-related aerosol source processeswas sought for in the data sets of 1996 and 2001 because they included fog drop size distributions. With increasing fog intensity modes in interstitial particle number concentrations appeared in particular in the size range around 80 nm that was nearly mode free in clear air. A second, dynamic approach revealed that Aitken mode concentrations increased strongly above their respective fog-period medians in both years before maximum drop numbers were reached in both years. We interpret the results of both approaches as strong indications of fog-related aerosol source processes as discussed in Leck and Bigg (1999) that need to be elucidated with further data from dedicated fog experiments in future Arctic expeditions in order to understand the life cycle of the aerosol over the high Arctic pack ice area.