Auflistung nach Autor:in "Lohmann, Ulrike"

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A synthesis of cloud condensation nuclei counter (CCNC) measurements within the EUCAARI network
(Copernicus, 2015) Paramonov, Mikhail; Kerminen, Veli-Matti; Gysel, Martin; Aalto, Pasi Pekka; Andreae, Meinrat O.; Asmi, Eija; Baltensperger, Urs; Bougiatioti, Aikaterini; Brus, David; Frank, Göran; Good, Nicholas; Gunthe, Sachin S.; Hao, Liqing; Irwin, Martin; Jaatinen, Antti; Jurányi, Zsófia; King, S. M.; Kortelainen, Aki; Kristensson, Adam; Lihavainen, Heikki; Kulmala, Markku; Lohmann, Ulrike; Martin, Scot T.; McFiggans, Gordon; Mihalopoulos, Nikolaos; Nenes, Athanasios; O'Dowd, Colin D.; Ovadnevaite, Jurgita; Petäjä, Tuukka; Pöschl, Ulrich; Roberts, Greg; Rose, Diana; Svenningsson, Birgitta; Swietlicki, Erik; Weingartner, Ernest; Whitehead, James; Wiedensohler, Alfred; Wittbom, Cerina; Sierau, Berko
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.
01A - Beitrag in wissenschaftlicher Zeitschrift
Aerosol processing in mixed‐phase clouds in ECHAM5‐HAM. Model description and comparison to observations
(Wiley, 15.04.2008) Hoose, Corinna; Lohmann, Ulrike; Stier, Philip; Verheggen, Bart; Weingartner, Ernest
The global aerosol‐climate model ECHAM5‐HAM has been extended by an explicit treatment of cloud‐borne particles. Two additional modes for in‐droplet and in‐crystal particles are introduced, which are coupled to the number of cloud droplet and ice crystal concentrations simulated by the ECHAM5 double‐moment cloud microphysics scheme. Transfer, production, and removal of cloud‐borne aerosol number and mass by cloud droplet activation, collision scavenging, aqueous‐phase sulfate production, freezing, melting, evaporation, sublimation, and precipitation formation are taken into account. The model performance is demonstrated and validated with observations of the evolution of total and interstitial aerosol concentrations and size distributions during three different mixed‐phase cloud events at the alpine high‐altitude research station Jungfraujoch (Switzerland). Although the single‐column simulations cannot be compared one‐to‐one with the observations, the governing processes in the evolution of the cloud and aerosol parameters are captured qualitatively well. High scavenged fractions are found during the presence of liquid water, while the release of particles during the Bergeron‐Findeisen process results in low scavenged fractions after cloud glaciation. The observed coexistence of liquid and ice, which might be related to cloud heterogeneity at subgrid scales, can only be simulated in the model when assuming nonequilibrium conditions.
01A - Beitrag in wissenschaftlicher Zeitschrift
Effect of photochemical ageing on the ice nucleation properties of diesel and wood burning particles
(Copernicus, 2013) Chou, Cédric; Kanji, Zamin A.; Stetzer, Olaf; Tritscher, Torsten; Chirico, Roberto; Heringa, Maarten F.; Weingartner, Ernest; Prévôt, André; Baltensperger, Urs; Lohmann, Ulrike
A measurement campaign (IMBALANCE) conducted in 2009 was aimed at characterizing the physical and chemical properties of freshly emitted and photochemically aged combustion particles emitted from a log wood burner and diesel vehicles: a EURO3 Opel Astra with a diesel oxidation catalyst (DOC) but no particle filter and a EURO2 Volkswagen Transporter TDI Syncro without emission aftertreatment. Ice nucleation experiments in the deposition and condensation freezing modes were conducted with the Portable Ice Nucleation Chamber (PINC) at three nominal temperatures, −30 °C, −35 °C and −40 °C. Freshly emitted diesel particles showed ice formation only at −40 °C in the deposition mode at 137% relative humidity with respect to ice (RHi) and 92% relative humidity with respect to water (RHw), and photochemical ageing did not play a role in modifying their ice nucleation behaviour. Only one diesel experiment where α-pinene was added for the ageing process, showed an ice nucleation enhancement at −35 °C. Wood burning particles also act as ice nuclei (IN) at −40 °C in the deposition mode at the same conditions as for diesel particles and photochemical ageing also did not alter the ice formation properties of the wood burning particles. Unlike diesel particles, wood burning particles form ice via condensation freezing at −35 °C whereas no ice nucleation was observed at −30 °C. Photochemical ageing did not affect the ice nucleation ability of the diesel and wood burning particles at the three different temperatures investigated but a broader range of temperatures below −40 °C need to be investigated in order to draw an overall conclusion on the effect of photochemical ageing on deposition/condensation ice nucleation across the entire temperature range relevant to cold clouds.
01A - Beitrag in wissenschaftlicher Zeitschrift
Hygroscopic properties of fresh and aged wood burning particles
(Elsevier, 2013) Martin, Maria; Tritscher, Torsten; Jurányi, Zsófia; Heringa, Maarten F.; Sierau, Berko; Weingartner, Ernest; Chirico, Roberto; Gysel, Martin; Prévôt, André S.H.; Baltensperger, Urs; Lohmann, Ulrike
01A - Beitrag in wissenschaftlicher Zeitschrift
Ice nuclei properties within a Saharan dust event at the Jungfraujoch in the Swiss Alps
(Copernicus, 04.10.2011) Chou, Cédric; Stetzer, Olaf; Weingartner, Ernest; Jurányi, Zsófia; Kanji, Zamin A.; Lohmann, Ulrike
The new portable ice nucleation chamber (PINC) developed by the Institute for Atmospheric and Climate Sciences of ETH Zurich was operated during two measurement campaigns at the high alpine research station Jungfraujoch situated at 3580 m a.s.l, in March and June 2009. During this time of the year, a high probability of Saharan dust events (SDE) at the Jungfraujoch has been observed. We used an impactor with a cutoff size of 1 μm aerodynamic diameter and operated the system at −31 °C and relative humidities of 127 % and 91 % with respect to ice and water, respectively. Investigation of the ambient number concentration of ice nuclei (IN) in the deposition nucleation mode and during a SDE in the free troposphere is reported. The results discussed in this paper are the first continuous IN measurements over a period of several days at the Jungfraujoch. The average IN concentration found during the campaign in March was 8 particles per liter whereas during the campaign in June, the average number concentration was higher up to 14 particles per liter. Two SDEs were detected on 15 and 16 June 2009. Our measurements show that the SDEs had IN number concentration up to several hundred per liter. We found the best correlation between the number concentration of the larger particle fraction measured by an optical particle counter and the IN number concentration during a Saharan dust event. This correlation factor is higher for particles larger than 0.5 μm meaning that a higher concentration of larger particles induced higher IN number concentration. No correlation could be found between the black carbon mass concentration and the variations in IN number concentration.
01A - Beitrag in wissenschaftlicher Zeitschrift
In situ determination of atmospheric aerosol composition as a function of hygroscopic growth
(Wiley, 30.08.2008) Herich, Hanna; Kammermann, Lukas; Gysel, Martin; Weingartner, Ernest; Baltensperger, Urs; Lohmann, Ulrike; Cziczo, Daniel J.
An in situ measurement setup to determine the chemical composition of aerosols as a function of hygroscopicity is presented. This has been done by connecting a custom‐built Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA) and an Aerosol Time‐of‐Flight Mass Spectrometer (ATOFMS), commercially available from TSI (Model 3800). Single particle bipolar mass spectra from aerosols leaving the HTDMA could thus be obtained as a function of the hygroscopic growth factor. For these studies the HTDMA was set at a relative humidity of 82% and particles with a dry diameter of 260 nm were selected. The setup was first laboratory tested, after which field experiments were performed. Two data sets were obtained during wintertime 2007 in Switzerland: the first in the urban Zurich environment and the other at the remote high alpine research station Jungfraujoch (JFJ). In Zurich, several thousand mass spectra were obtained in less than 2 days of sampling due to a high aerosol loading. At the JFJ, due to low particle concentrations in free tropospheric air masses, a longer sampling period was required. Both in Zurich and at the JFJ, two different growth factor modes were observed. Results from these two locations show that most aerosol particles were a mixture of several compounds. A large contribution of organics and combustion species was found in the less hygroscopic growth mode for both locations. Noncombustion refractory material (e.g., metals, mineral dust, and fly ash) was also highly enhanced in the nonhygroscopic particles. Sulfate, normally considered highly soluble, was found to be a constituent in almost all particles independent of their hygroscopic growth factor.
01A - Beitrag in wissenschaftlicher Zeitschrift
Sensitivity estimations for cloud droplet formation in the vicinity of the high-alpine research station Jungfraujoch (3580 m a.s.l.)
(Copernicus, 2015) Hammer, Emanuel; Bukowiecki, Nicolas; Luo, Beiping; Lohmann, Ulrike; Marcolli, Claudia; Weingartner, Ernest; Baltensperger, Urs; Hoyle, Christopher R.
Aerosol radiative forcing estimates suffer from large uncertainties as a result of insufficient understanding of aerosol–cloud interactions. The main source of these uncertainties is dynamical processes such as turbulence and entrainment but also key aerosol parameters such as aerosol number concentration and size distribution, and to a much lesser extent, the composition. From June to August 2011 a Cloud and Aerosol Characterization Experiment (CLACE2011) was performed at the high-alpine research station Jungfraujoch (Switzerland, 3580 m a.s.l.) focusing on the activation of aerosol to form liquid-phase clouds (in the cloud base temperature range of −8 to 5 °C). With a box model the sensitivity of the effective peak supersaturation (SSpeak), an important parameter for cloud activation, to key aerosol and dynamical parameters was investigated. The updraft velocity, which defines the cooling rate of an air parcel, was found to have the greatest influence on SSpeak. Small-scale variations in the cooling rate with large amplitudes can significantly alter CCN activation. Thus, an accurate knowledge of the air parcel history is required to estimate SSpeak. The results show that the cloud base updraft velocities estimated from the horizontal wind measurements made at the Jungfraujoch can be divided by a factor of approximately 4 to get the updraft velocity required for the model to reproduce the observed SSpeak. The aerosol number concentration and hygroscopic properties were found to be less important than the aerosol size in determining SSpeak. Furthermore turbulence is found to have a maximum influence when SSpeak is between approximately 0.2 and 0.4 %. Simulating the small-scale fluctuations with several amplitudes, frequencies and phases, revealed that independently of the amplitude, the effect of the frequency on SSpeak shows a maximum at 0.46 Hz (median over all phases) and at higher frequencies, the maximum SSpeak decreases again.
01A - Beitrag in wissenschaftlicher Zeitschrift
Subarctic atmospheric aerosol composition: 2. Hygroscopic growth properties
(Wiley, 10.07.2009) Herich, Hanna; Kammermann, Lukas; Friedman, Beth; Gross, Deborah S.; Weingartner, Ernest; Lohmann, Ulrike; Spichtinger, Peter; Gysel, Martin; Baltensperger, Urs; Cziczo, Daniel J.
Subarctic aerosols were sampled during July 2007 at the Abisko Scientific Research Station Stordalen site in northern Sweden with an instrument setup consisting of a custom‐built Hygroscopicity Tandem Differential Mobility Analyzer (HTDMA) connected in series to a single particle mass spectrometer. Aerosol chemical composition in the form of bipolar single particle mass spectra was determined as a function of hygroscopic growth both in situ and in real time. The HTDMA was deployed at a relative humidity of 82%, and particles with a dry mobility diameter of 260 nm were selected. Aerosols from two distinct air masses were analyzed during the sampling period. Sea salt aerosols were found to be the dominant particle group with the highest hygroscopicity. High intensities of sodium and related peaks in the mass spectra were identified as exclusive markers for large hygroscopic growth. Particles from biomass combustion were found to be the least hygroscopic aerosol category. Species normally considered soluble (e.g., sulfates and nitrates) were found in particles ranging from high to low hygroscopicity. Furthermore, the signal intensities of the peaks related to these species did not correlate with hygroscopicity.
01A - Beitrag in wissenschaftlicher Zeitschrift
The effect of physical and chemical aerosol properties on warm cloud droplet activation
(Copernicus, 2006) McFiggans, Gordon B.; Artaxo, Paulo; Baltensperger, Urs; Coe, Hugh; Facchini, Maria Cristina; Feingold, Graham; Fuzzi, Sandro; Gysel, Martin; Laaksonen, Ari; Lohmann, Ulrike; Mentel, Thomas F.; Murphy, Daniel M.; O'Dowd, Colin D.; Snider, Jefferson R.; Weingartner, Ernest
Abstract. The effects of atmospheric aerosol on climate forcing may be very substantial but are quantified poorly at present; in particular, the effects of aerosols on cloud radiative properties, or the "indirect effects" are credited with the greatest range of uncertainty amongst the known causes of radiative forcing. This manuscript explores the effects that the composition and properties of atmospheric aerosol can have on the activation of droplets in warm clouds, so potentially influencing the magnitude of the indirect effect. The effects of size, composition, mixing state and various derived properties are assessed and a range of these properties provided by atmospheric measurements in a variety of locations is briefly reviewed. The suitability of a range of process-level descriptions to capture these aerosol effects is investigated by assessment of their sensitivities to uncertainties in aerosol properties and by their performance in closure studies. The treatment of these effects within global models is reviewed and suggestions for future investigations are made.
01A - Beitrag in wissenschaftlicher Zeitschrift
Water uptake of clay and desert dust aerosol particles at sub- and supersaturated water vapor conditions
(Royal Society of Chemistry, 01.04.2009) Herich, Hanna; Tritscher, Torsten; Wiacek, Aldona; Gysel, Martin; Weingartner, Ernest; Lohmann, Ulrike; Baltensperger, Urs; Cziczo, Daniel J.
Airborne mineral dust particles serve as cloud condensation nuclei (CCN), thereby influencing the formation and properties of warm clouds. It is therefore of atmospheric interest how dust aerosols with different mineralogy behave when exposed to high relative humidity (RH) or supersaturation (SS) with respect to liquid water. In this study the subsaturated hygroscopic growth and the supersaturated cloud condensation nucleus activity of pure clays and real desert dust aerosols were determined using a hygroscopicity tandem differential mobility analyzer (HTDMA) and a cloud condensation nuclei counter (CCNC), respectively. Five different illite, montmorillonite and kaolinite clay samples as well as three desert dust samples (Saharan dust (SD), Chinese dust (CD) and Arizona test dust (ATD)) were investigated. Aerosols were generated both with a wet and a dry disperser. The water uptake was parameterized via the hygroscopicity parameter k. The hygroscopicity of dry generated dust aerosols was found to be negligible when compared to processed atmospheric aerosols, with CCNC derived k values between 0.00 and 0.02 (the latter corresponds to a particle consisting of 96.7% by volume insoluble material and B3.3% ammonium sulfate). Pure clay aerosols were generally found to be less hygroscopic than natural desert dust particles. The illite and montmorillonite samples had k B 0.003. The kaolinite samples were less hygroscopic and had k = 0.001. SD (k = 0.023) was found to be the most hygroscopic dry-generated desert dust followed by CD (k = 0.007) and ATD (k = 0.003). Wet-generated dust showed an increased water uptake when compared to dry-generated samples. This is considered to be an artifact introduced by redistribution of soluble material between the particles. Thus, the generation method is critically important when presenting such data. These results indicate any atmospheric processing of a fresh mineral dust particle which leads to the addition of more than B3% soluble material will significantly enhance its hygroscopicity and CCN activity.
01A - Beitrag in wissenschaftlicher Zeitschrift