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    Relationship between temperature and apparent shape of pristine ice crystals derived from polarimetric cloud radar observations during the ACCEPT campaign
    (München : European Geopyhsical Union, 2016) Myagkov, Alexander; Seifert, Patric; Wandinger, Ulla; Bühl, Johannes; Engelmann, Ronny
    This paper presents first quantitative estimations of apparent ice particle shape at the top of liquid-topped clouds. Analyzed ice particles were formed under mixed-phase conditions in the presence of supercooled water and in the temperature range from −20 to −3 °C. The estimation is based on polarizability ratios of ice particles measured by a Ka-band cloud radar MIRA-35 with hybrid polarimetric configuration. Polarizability ratio is a function of the geometrical axis ratio and the dielectric properties of the observed hydrometeors. For this study, 22 cases observed during the ACCEPT (Analysis of the Composition of Clouds with Extended Polarization Techniques) field campaign were used. Polarizability ratios retrieved for cloud layers with the cloud-top temperatures of  ∼ −5,  ∼ −8,  ∼ −15, and  ∼ −20 °C were 1.6, 0.9, 0.6, and 0.9, respectively. Such values correspond to prolate, quasi-isotropic, oblate, and quasi-isotropic particles, respectively. Data from a free-fall chamber were used for the comparison. A good agreement of detected apparent shapes with well-known shape–temperature dependencies observed in laboratories was found. Polarizability ratios used for the analysis were estimated for areas located close to the cloud top, where aggregation and riming processes do not strongly affect ice particles. We concluded that, in microwave scattering models, ice particles detected in these areas can be assumed to have pristine shapes. It was also found that even slight variations of ambient conditions at the cloud top with temperatures warmer than  ∼ −5 °C can lead to rapid changes of ice crystal shape.
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    Phase transition observations and discrimination of small cloud particles by light polarization in expansion chamber experiments
    (München : European Geopyhsical Union, 2016) Nichman, Leonid; Fuchs, Claudia; Järvinen, Emma; Ignatius, Karoliina; Höppel, Niko Florian; Dias, Antonio; Heinritzi, Martin; Simon, Mario; Tröstl, Jasmin; Wagner, Andrea Christine; Wagner, Robert; Williamson, Christina; Yan, Chao; Connolly, Paul James; Dorsey, James Robert; Duplissy, Jonathan; Ehrhart, Sebastian; Frege, Carla; Gordon, Hamish; Hoyle, Christopher Robert; Kristensen, Thomas Bjerring; Steiner, Gerhard; McPherson Donahue, Neil; Flagan, Richard; Gallagher, Martin William; Kirkby, Jasper; Möhler, Ottmar; Saathoff, Harald; Schnaiter, Martin; Stratmann, Frank; Tomé, António
    Cloud microphysical processes involving the ice phase in tropospheric clouds are among the major uncertainties in cloud formation, weather, and general circulation models. The detection of aerosol particles, liquid droplets, and ice crystals, especially in the small cloud particle-size range below 50 μm, remains challenging in mixed phase, often unstable environments. The Cloud Aerosol Spectrometer with Polarization (CASPOL) is an airborne instrument that has the ability to detect such small cloud particles and measure the variability in polarization state of their backscattered light. Here we operate the versatile Cosmics Leaving OUtdoor Droplets (CLOUD) chamber facility at the European Organization for Nuclear Research (CERN) to produce controlled mixed phase and other clouds by adiabatic expansions in an ultraclean environment, and use the CASPOL to discriminate between different aerosols, water, and ice particles. In this paper, optical property measurements of mixed-phase clouds and viscous secondary organic aerosol (SOA) are presented. We report observations of significant liquid–viscous SOA particle polarization transitions under dry conditions using CASPOL. Cluster analysis techniques were subsequently used to classify different types of particles according to their polarization ratios during phase transition. A classification map is presented for water droplets, organic aerosol (e.g., SOA and oxalic acid), crystalline substances such as ammonium sulfate, and volcanic ash. Finally, we discuss the benefits and limitations of this classification approach for atmospherically relevant concentrations and mixtures with respect to the CLOUD 8–9 campaigns and its potential contribution to tropical troposphere layer analysis.