6th Workshop – Microphysics of ice clouds
Vienna- Austria 7th of April 2018
Book of Abstracts
Preface
Dear Workshop Participant, It is my pleasure to welcome you to Vienna at our 6th workshop 'Microphysics of Ice Clouds'. We will bring together three communities of atmospheric ice research: field measurements, laboratory studies and modellers. The joint topic is the ice nucleation in clouds. We will focus on recent observations, and open questions concerning ice formation and development in the atmosphere discussing experimental and theoretical methods including chemistry and microphysics. A particular focus will be heterogeneous ice nucleation. The development of a detailed understanding of ice clouds in the atmosphere relies on the combined use of field studies, modelling at a multitude of scales, and laboratory studies that provide the necessary fundamentals. Atmospheric ice is studied by remote sensing methods from the ground, from airplanes and satellites, or in situ from airborne platforms such as aircraft and balloons. While such observations are essential, the various methods often lack sufficient access to fundamental physic-chemical parameters of ice particles and the involved nucleation process. On the other hand, laboratory studies are usually aimed at understanding the fundamentals of the underlying processes such as the details of the nucleation process, because they can be performed under well controlled conditions. Hence, under these controlled conditions the impact of individual parameters on the ice formation process can be determined. Theoretical and numerical models are then required to transfer the knowledge of laboratory and field studies into small and large-scale models using sensible parameterizations. Moreover, the influence and impact of the nature of pre-existing aerosol particles on ice nucleation efficiency, ice microstructure and ice cloud dynamics are one of the least understood parameters in cloud microphysics. The knowledge of chemists, biologists and crystallographers about the aerosol composition has to be combined with the ice dynamic models of physicists, meteorologists and computational modellers to gain a better understanding of the whole process. For these reasons it seems viable for progress in this area to bring together scientists from various (sub-) disciplines and foster discussions between them. Given the importance of understanding the atmospheric ice nucleation process for various atmospheric applications, e.g. the modelling precipitation and for a representation of clouds in climate models, we believe the topic of the workshop “Microphysics of Ice Clouds” is of high scientific interest for scientists from various disciplines such as meteorology, chemistry, physics, and biology. A workshop provides an ideal platform for more detailed and, thus, deeper interaction between the different communities and provides the opportunity to bring together scientists from the different fields of ice research. Moreover, in contrast to a regular session at the EGU General Assembly with a rapid sequence of contributed talks (typically 12min + 3min of questions), the workshop will provide more time for discussion. This may help abolishing uncertainties and prejudices existing between scientists from different disciplines, in particular for PhD students and postdocs who represent the next generation of scientists. Vienna 7th April 2018 Hinrich Grothe
Local Organizer Prof. Dr. Hinrich Grothe TU Wien Institute of Materials Chemistry www.imc.tuwien.ac.at Email: [email protected] Tel.: +43-664-605886522
Location
Italian Culture Institute
The workshop is held in the "Italian Culture Institute - Istituto Italiano di Cultura" at Ungargasse 43, 1030 Vienna, which is easily accessible by public transport.
Istituto Italiano di Cultura
Map:
Rochusgasse to Ungargasse
Transportation
Sessions Saturday 7th April
12:00 - 13:00 Registration and Buffet
13:00 - 13:10 Opening of the workshop
Hinrich Grothe (Vienna University of Technology)
Ernst Kanitz (Italian Culture Institute, Vienna)
Mixed Session
13:10 - 13:25 1st Talk Philipp Baloh Spectroscopic investigations on organic compounds in desert dust particles
13:25 - 13:30 Discussion
13:30 - 13:45 2nd Talk Ruihao Zhu A Laboratory Study on Immersion Freezing Behavior of Aerosols in Beijing
13:45 - 13:50 Discussion
13:50 - 14:05 3rd Talk Max Port Observations of ice-clouds from deep convective outflow during the Asian monsoon
14:05 - 14:10 Discussion
14:10 - 14:25 4th Talk Jie Chen Freezing activity of droplets containing Humic-acid like substances (HULIS)
14:25 - 14:30 Discussion 14:30 - 14: 45 Break Out Discussion (Coffee &Cakes)
Laboratory Measurements I
14:45 - 15:00 1st Talk Shizuo Fu The Efficiency Spectrum of Ice-Nucleating
Particles and Its Application to the Parameterization of Ice Formation
15:00 - 15:05 Discussion
15:05 - 15:20 2nd Talk Huan Yu Yang Towards the surface science of ice nucleation
on aqueous organic solutions and solid substrates
15:20 - 15:25 Discussion
15:25 - 15:40 3rd Talk Willi Pose Raman investigations on several classes of ice nucleation active aerosols
15:40 - 15:45 Discussion 15:45 - 16:00 Break Out Discussion (Coffee &Cakes)
Laboratory Measurements II
16:00 - 16:15 1st Talk Dominik Heger Looking for the relevance of laboratory experiment to ice clouds
16:15 - 16:20 Discussion
16:20 - 16:35 2nd Talk Jan Voráč Spectroscopy of electrical discharges in contact with water/ice
16:35 - 16:40 Discussion
16:40 - 16:55 3rd Talk Jan Voráč Measurement of reactive radical species in discharges in contact with water/ice
16:55 - 17:00 Discussion 17:00 - 17:15 Break Out Discussion (Coffee &Cakes)
Field Measurements I
17:15 - 17:30 1st Talk Claudia Mignani
A case study of biological ice nucleating particles in the Arctic
17:30 - 17:35 Discussion
17:35 - 17:50 2nd Talk Bruce Moffett Significance of Fresh Water Ice Nucleating
Particles in USA, UK and Mainland European Rivers
17:50 - 17:55 Discussion
17:55 - 18:10 3rd Talk Jessie Creamean
Using spectra characteristics to define ice nucleating particle populations from north and
south of the Alps 18:10 - 18:15 Discussion 18:15 - 18:30 Break Out Discussion (Coffee &Cakes)
Field Measurements II
18:30 - 18:45 1st Talk Veronika Wolf Two totally different Arctic cirrus clouds in February - A case study
18:45 - 18:50 Discussion
18:50 - 19:05 2nd Talk Vaughan Phillips
Raindrop-freezing fragmentation in natural clouds
19:05 - 19:10 Discussion
19:10 - 19:25 3rd Talk Durgesh Nandan Piyush
Diurnal variation of cloud ice water path as observed from SAPHIR onboard Megha-
Tropiques 19:25 - 19:30 Discussion
19:30 - 19:45 4th Talk David Delene Research Aircraft Observations of the Micro-physics of Ice Clouds
19:45 - 19:50 Discussion 19:50 - 20:00 General Discussion 20:00 – 22:00 Dinner & After-Dinner Workshop (optional)
Spectroscopic investigations on organic compounds in desert dust particles
Philipp Baloh1*, Yvonne Boose2,3*, Michael Plötze4, Ulrike Lohmann2, Zamin Kanji2, and Hinrich Grothe1
1Institute of Materials Chemistry, TU Wien, Vienna, Austria;
2ETH Zürich, Institute for Atmospheric and Climate Science, Zürich, Switzerland;
3German Aerospace Center (DLR), Institute for Atmospheric Physics, Oberpfaffenhofen;
4ETH Zürich, Institute for Geotechnical Engineering, Zürich.
* Email: [email protected], [email protected] Mineral dust particles are the most abundant ice nucleating particles (INPs) found in the
atmosphere. Their mineralogical composition in part dictates if they can act as strong INPs or
not. Certain minerals such as microcline show an exceptionally strong ice nucleating
potential, yet its presence in a desert dust particle alone does not seem to be the determining
factor for ice nucleation. In a mixed phase particle, strong ice nucleating minerals may not
come to their full potential due to chemical and mechanical aging that can inactivate their
nucleation sites or due to an interference with compounds that coat the particles, yet only
contribute very little to its overall mass. Carbonic acids, for example, are well known to
hinder ice nucleation to a certain extent and other compounds may simply be able to shield, or
react with the surface in a way that antagonizes the nucleation active sites. What kind of
surface chemicals could be present on dust particles can vary highly depending on the source
of the particle but also on the atmospheric conditions it encounters during transport.
In this study, we investigate how mineralogy, crystal water, and heat labile organic
compounds on dust particles affect the ice nucleating behavior of desert dust collected from
the soil or after atmospheric transport. Before and after heating three dust samples to 573 K,
we measured their ice active surface site density (ns) in the deposition and condensation mode
and used X-ray diffraction (XRD), and Raman- and Infrared- spectroscopy to search for the
cause of observed differences in ns. Infrared spectroscopy was conducted on the bulk material
and Raman spectroscopy on single particles by means of micro-Raman mapping of impacted
dust. Indications for heat labile organic compounds were found in two samples as well as
indications for soot. However, also the inorganic composition in the form of crystal water –
and its subsequent change in mineralogic composition due to its loss – seems to play a role for
one sample. While the ns of this sample increased after heating, in a second sample the
release of heat labile organic compounds led to suppression of the ice nucleation ability. Our
study shows that apart from mineralogy, other factors such as organics and crystal water can
alter the ice nucleation behavior of desert dust during atmospheric transport in various ways.
A Laboratory Study on Immersion Freezing Behavior of Aerosols in Beijing
Ruihao Zhu, Yangze Ren, Shizuo Fu, and Huiwen Xue
Department of Atmospheric and Oceanic Sciences, School of Physics, Peking University, China ([email protected])
This study investigates the immersion freezing behavior of aerosols in Beijing. Three types of
local aerosols are considered in the experiments: dry deposition aerosols, pollen, and soil
particles. We also investigate the immersion freezing behavior of montmorillonite, to compare
with the local aerosols. The experimental data show that there exist different onset
temperatures for different types of aerosols, above which freezing does not occur. The
average onset temperatures for dry deposition aerosols, pollen, soil particles, and
montmorillonite are respectively -13.8℃, -13.1℃, -14.3℃, and -14.5℃. We then use a θ-pdf
scheme to parameterize the freezing process. This scheme assumes that the cosine of contact
angle follows a lognormal distribution. The calculated curves fit well with the data points.
The fitting parameters show that the nucleation efficiencies of different aerosols are quite
different. There is a 5000-10000 times difference in nucleation rate between dry deposition
aerosols and soil particles. Results of this study indicate that pollen and dry deposition
aerosols are more efficient than soil particles in immersion freezing mode.
Observations of ice-clouds from deep convective outflow during the Asian monsoon
Max Port1, Oliver Schlenczek1,6, Christoph Mahnke1, Ralf Weigel2, Silvia Viciani3, Francesco D'Amato3, Gennady Belyaev4, Fred Stroh5, Stephan Borrmann1,2
1Max-Planck lnstitute for Chemistry, Mainz, Germany
2University of Mainz, Germany
3lnstituto Nazionale di Ottica, Firenze, ltaly
4Myasishchev Design Bureau, Zhukovsky, Russia
5Forschungszentrum Juelich, Juelich, Germany
6Now at Max Planck lnstitute for Dynamics and Self-Organization, Goettingen, Germany
The StratoClim field campaign was carried out using the Russian high-altitude aircraft M-55
Geophysica and took place during the monsoon season during July and August 2017 in Nepal.
A total number of 8 flights (≈ 30 flight hours) were carried out within the Asian Monsoon
Anticyclone (AMA) over Nepal, lndia and Bangladesh, reaching up to altitudes of 20
kilometers thereby. A set of 5 different underwing cloud probes (including a holographic
device) covers a particle size diameter range from 2.5µm - 6400µm (time resolution: 1Hz,
uncertainty of number concentrations ≈ 10%). We present data of size distributions and
number densities for ice particles sampled during approximately 7 hours of cloud passes in
the sub-tropical UTLS region above 200hPa.
During Flight 8 on August 10th the aircraft encountered an outflow event of a large convective
system over northern India. As shown in the figure, combining results from the ice particle
instruments and the carbon monoxide measurements from COLD (time resolution: 1Hz,
sensitivity: 2 ppb, uncertainty: 6%), we see periods where increased cloud particle number
concentrations (up to 10 particles per cm3) and elevated CO mixing ratios (up to 100 ppb)
coincide. The observation of high CO mixing ratios is indicative for low level air carried aloft
by deep convection. ln the presentation the observed ice particle size distributions, their
number densities and their shapes at the cold point tropopause are shown for pressure levels
of around 85 hPa, and in particular from the region of the Asian Monsoon anticyclone.
Freezing activity of droplets containing Humic-acid like substances (HULIS)
Jie Chen1, Zhijun Wu1, Yao Bai1, Min Hu1, and Heike Wex2
1Peking University, Beijing, China, ([email protected]).
2Leibniz Institute for Tropospheric Research, 04318, Leipzig, Germany
Currently, the ice nucleation efficiency of organic materials is not well-recognized. HULIS are important surface- active components of water soluble organic carbon, its presence may depress the surface tension of droplets, therefore, impacting the cloud droplet formation and the subsequent ice crystallization. In the present study, a recently developed and well calibrated optical droplet cooling array was used to measure the ice nucleating efficiency of droplets containing HULIS derived from ambient particulate matters, in parallel with the determination of surface tension by a drop shape analyzer (DSA-30) and chemical composition by an ESI-Orbitrap mass spectrometry. The HULIS were extracted from particles collected in the atmosphere over Beijing using a well-established method (Lin et al., 2010), and then dissolved with Milli-Q water. The HULIS carbon content of each sample was quantified by a total organic carbon analyzer. The experiments showed that 1μl droplet containing HULIS (15.8 - 96.7 mg C/L) frozen in the temperature range from -9°C to -22°C, which was above the pure water background and the typical homogenous freezing temperature (below -38°C). Droplets with higher HULIS content (96.7 mg C/L, surface tension 66.3 mN/m) frozen at a lower temperature in contrast to those with lower HULIS carbon (15.8-37.8 mg C/L, surface tension 70.2-71.5 mN/m). The freezing activities of mixture of ammonium sulfate and HULIS and related to chemical composition of HULIS will also be presented.
Lin, P., Huang, X.-F., He, L.-Y., and Zhen Yu, J.: Abundance and size distribution of HULIS in ambient aerosols at a rural site in South China, J. Aerosol Sci., 41, 74-87, doi:10.1016/j.jaerosci.2009.09.001, 2010.
The Efficiency Spectrum of Ice-Nucleating Particles and Its Application to the Parameterization of Ice Formation
Shizuo Fu1 and Huiwen Xue2
1Peking University, Department of Atmospheric and Oceanic Sciences, China ([email protected]);
2Peking University, Department of Atmospheric and Oceanic Sciences, China ([email protected]);
Ice-nucleating particles (INPs) can heterogeneously nucleate ice crystals above 235 K. They
hence play a very important role in the evolution of mixed-phase clouds, and subsequently
exert a significant influence on the hydrological cycle and the radiative balance of the earth
system. However, due to its complexity, heterogeneous nucleation has not been well
understood, leading to remarkable differences in the parameterizations of heterogeneous
nucleation. These differences have been found to be responsible for the differences in cloud
fraction and therefore cloud radiative forcing among the models.
Based on the measurement performed with the continuous-flow diffusion chamber (CFDC),
this study derived an efficiency spectrum of INP. The spectrum shows that INP concentration
exponentially increases with decreasing efficiency. The efficiency spectrum was then
implemented into the classical nucleation theory (CNT) to compare the ice concentration
predicted by the CNT with that predicted by the deterministic theory (DT) at different cooling
rates. Results show that when the cooling rate decreases from the typical cooling rate for
convective clouds (~1 K min-1) to the typical cooling rate of stratiform clouds (~1 K day-1),
the ice concentration predicted by the CNT becomes progressively higher than that predicted
by the DT. This is because CNT allows the INPs that are not detected by the CFDC at the
current temperature to contribute to the ice formation while the DT does not. This study
suggests that the CNT, into which the efficiency spectrum of INP is incorporated, should be
used to parameterize ice formation.
Towards the surface science of ice nucleation on aqueous organic solutions and solid substrates
Huan Yu Yang1,2, Artiglia Luca1, Fabrizio Orlando1, ShuZhen Chen1,2, XiangRui Kong1, and Markus Ammann1
1Paul Scherrer Institut, Villigen, Switzerland,
2ETH Zürich, Zürich, Switzerland,
The nucleation of ice is an important process in chemistry, physics and atmospheric science. Although ice nucleation has been studied since long, our understanding of ice nucleation is still far from complete, particularly from a molecular point of view. The hydrogen bonding structure of H2O can be significantly different between liquid water to ice. This structure is responsible for most of the difference in physical and chemical properties between the different aggregation states of water. The difference between the hydrogen bonding structure of liquid water and ice can be experimentally observed by near edge X-ray absorption fine structure (NEXAFS) spectroscopy at the oxygen K-edge, because it involves resonant transitions into unoccupied molecular orbitals, which are very sensitive to the nearest neighbors of oxygen atoms. NEXAFS spectroscopy can be performed in electron yield mode, in which Auger electrons emitted upon initial core hole excitation are detected, which provides a surface sensitive NEXAFS spectrum. Experiments reported in this work were performed at the near ambient photoelectron spectroscopy endstation (NAPP) at the SIM and NANOXAS beamline at the Swiss Light Source (PSI, SLS). Since it has been suggested that some organic compounds have the potential to modify the structure of water that influences the nucleation of ice, we have measured electron yield NEXAFS spectra from a liquid jet of aqueous solution containing tetrabutylammonium bromide (TBAB). The O K-edge spectra exhibit a clear change in the relative features. These features represent hydrogen bonding at different level, indicating that the cationic head group of TBAB induces a significant variation of the hydrogen bonding network near the surface of the aqueous solution. On the other hand, the hydrogen bonding structure of adsorbed water on a solid substrate may control deposition nucleation, which is another pathway of heterogeneous ice nucleation. The hydrogen bonding structure may be affected by short and long range interactions between the substrate and the adsorbed water molecules. As a first approach, we have measured electron yield NEXAFS spectra of adsorbed water on graphite and titanium dioxide (TiO2) under subsaturated conditions with respect to ice. Under isobaric conditions and by varying the temperature of the sample, we can change the relative humidity, which leads to varying amounts of adsorbed water in equilibrium between the substrate and water vapor. Preliminary results show that, under different relative humidity, the weakly and strongly coordinated OH bond of adsorbed water on TiO2 and graphite show different contributions to the Auger electron yield NEXAFS spectrum, that is, the resonant transitions near the oxygen K-edge vary with relative humidity and temperature. We attribute this to the modification of the organization of water molecules in response to the interactions with the solid substrate. In view of the application of the NEXAFS technique, we believe it opens up a powerful tool to address the surface science of ice nucleation in the future.
Raman investigations on several classes of ice nucleation active aerosols
Willi Pose
University of Innsbruck, Institute of Physical Chemistry, Innrain 52c, A-6020 Innsbruck, Austria
Heterogeneous ice nucleation is the major cause for solid and liquid precipitation via ice
cloud and mixed phase cloud formation. Aerosol particles in suitable size and composition
trigger thereby the phase change of supercooled liquid water to hexagonal ice. Several classes
of ice active aerosols (IN) are known which nucleate ice at different temperatures.
Quantitatively, IN are well described though the heterogeneous freezing path understanding
lacks micro physical findings. The class of organic IN acts on the warmer temperature range.
Some amino acids are active for temperatures up to 267 K. With Alanine, Serine and Tyrosine
in immersion mode (respectively) is a Raman-microscopy observation performed to learn of
how those IN transform liquid water structure to ice. Therefore the changes on the Raman
shift spectra of the translational and OH vibrations within a water droplet are evaluated.
Additionally the influences by some insoluble IN are investigated. The soluble amino acids in
pure water at 268 K raise the shoulder of the OH-peak and the translational peak. This
happens in pure water at 12 K (present experiment) lower temperature, which indicates the
step before freezing. Comparing the translation peak and the OH-Peak it is a mirrored
behaviour found. The insoluble materials do not stimulate the vibrational modes of water like
the amino acids what suggests a different freezing mechanism or is a difference in freezing
mode.
Looking for the relevance of laboratory experiment to ice clouds
Dominik Heger
Department of Chemistry and RECETOX, Faculty of Science, Masaryk University, Kamenice 5/A8, 625 00 Brno, Czech Republic;
[email protected], http://hegerd.sci.muni.cz/
I wish to share our spectroscopic and microscopic observations if ice impurities and to
question their relevance to ice clouds chemistry and physics. We apply UV-Vis and
fluorescence spectroscopies to learn about the ice surface acidities1-3 and compounds
aggregation.4,5 In recent environmental scanning electron microscopy studies details of the
evaporation of water from the salty ice (frost-flowers) showed the presence of microscopic
crystals of salt.6
(1) Vetráková, Ľ.; Vykoukal, V.; Heger, D. International Journal of Pharmaceutics 2017,
530, 316.
(2) Heger, D.; Klanova, J.; Klan, P. Journal of Physical Chemistry B 2006, 110, 1277.
(3) Krausko, J.; Runštuk, J.; Neděla, V.; Klán, P.; Heger, D. Langmuir 2014, 30, 5441.
(4) Krausko, J.; Malongwe, J. K. E.; Bičanová, G.; Klán, P.; Nachtigallová, D.; Heger, D.
The Journal of Physical Chemistry A 2015, 119, 8565.
(5) Heger, D.; Jirkovsky, J.; Klan, P. Journal of Physical Chemistry A 2005, 109, 6702.
(6) Yang, X.; Neděla, V.; Runštuk, J.; Ondrušková, G.; Krausko, J.; Vetráková, Ľ.; Heger,
D. Atmos. Chem. Phys. 2017, 17, 6291.
Spectroscopy of electrical discharges in contact with water/ice
Jan Voráč, Pavel Dvořák, Martina Mrkvičková
Department of Physical Electronics, Faculty of Science, Masaryk University Kotlářská 2, Brno 611 37, Czech Republic
Figure 1. An overview spectrum of a streamer discharge ignited in ambient air in contact with
ice surface. Note the different axes scales.
Plasma in the form of electrical discharge is readily formed during various occasions in
everyday life, including thunderstorms or corona discharges on high-voltage conductors.
Plasma is also often a source of radiation which can be spectroscopically analysed and
provide useful information about the processes taking place. In [1] we have analysed
spectrum of microdischarges formed in contact with liquid water and observed strongly
inequilibiral distribution of quantum states, caused mainly by violent dissociation of water
molecules.
In Figure 1 a preliminary measurement of emission of microdischarges ignited in ambient air
and propagating along an ice surface is presented. The spectrum is absolutely dominated by
nitrogen second positive system, or N2 (C 3Πu → B 3Πg) electronic transition in the range 290 -
450 nm. Between 500 and 1100, much weaker emission of N2 (B 3Πg → A 3Σu+), or first positive
system, was observed. According to the first analyses, the vibrational distribution of nitrogen
molecules can be vaguely described by vibrational temperature around 4000 K, but deviations
from Boltzmann distribution were present
[1] Voráč, J., Synek, P., Procházka, V., & Hoder, T. (2017). State-by-state emission spectra
fitting for non- equilibrium plasmas: OH spectra of surface barrier discharge at argon/water
interface. Journal of Physics D: Applied Physics, 50(29), 294002.
Measurement of reactive radical species in discharges in contact with water/ice
Pavel Dvořák, Jan Voráč, Vojtěch Procházka, Martina Mrkvičková
Department of Physical Electronics, Faculty of Science, Masaryk University, Kotlářská 2, Brno 611 37, Czech Republic
Plasma generated by means of electric discharges produces number of reactive radical species
that can interact with surfaces of solid or liquid objects that are in contact with plasma and
initiate number of chemical and physical reactions at the surfaces or inside liquid
environments. Plasma ignited in air with contact with aqueous solutions presents an actual
topic of research that is motivated by research in the field of plasma medicine and by
questions related to the processes occurring in the plasma at the gas-liquid interface. Logical
extension of this field is the research of plasma that is in contact with ice, i.e. research of field
that is connected with problematics of both hydrometeors in thunderstorms and removal of
toxic agents from water solutions.
Since radical species usually play the key-role in plasma-surface interactions, we apply the
fluorescence method for their detection. Whereas single-photon excitation is used for
detection of most molecular species (including the OH radical), two-photon excitation is
required for detection of most atomic species (including atomic radicals H, N and O).
Actually, we deal with fluorescence measurements in plasma that is in contact with liquid
water or with high concentration of water vapour and our plan is to continue with
measurements in plasma ignited at ice surface. The interaction of the excitation laser beam
with the ice surface produces number of parasitic signals. Fortunately, we have solved this
problematic in analogical discharges that were in contact with various solid or liquid surfaces
[1]. We observed e.g. generation of both OH and H radicals in plasma above water surface.
Concentration of atomic H radicals in plasma with water vapour decreased strongly with an
increase of water vapour content due to the reaction H + H2O <-> OH + H2 [2].
[1] M. Mrkvičková, J. Ráheľ, P. Dvořák, D. Trunec, T. Morávek: Plasma Sources, Science
and Technology, 25 (2016), 055015.
[2] V. Procházka, Z. Tučeková, P. Dvořák, D. Kováčik, P. Slavíček, A. Zahoranová, J. Voráč:
Plasma Sources, Science and Technology, 27 (2018), 015001.
A case study of biological ice nucleating particles in the Arctic
Claudia Mignani1, Daniel Weber2, Jann Schrod2, Lukas Zimmermann1, Heinz Bingemer2, Franz Conen1, Christine Alewell1
1 Department of Environmental Sciences, University of Basel, 4056 Basel, Switzerland ([email protected])
2 Institute for Atmospheric and Environmental Sciences, Goethe University, 60438 Frankfurt/Main, Germany
The formation of ice in clouds impacts Earth’s water and energy budget1. A prerequisite for initial
phase transition from liquid water to ice in mixed-phase clouds is the presence of ice nucleating
particles (INPs)2. At temperatures above - 15°C, biological INPs are likely the dominant particles
initiating the liquid-ice phase transition in clouds3. However, the sensitivity of cloud glaciation to
biological INPs is still not fully understood. Here, we present preliminary results of INP
concentrations and characteristics derived from atmospheric aerosols sampled during a 7-day field
campaign at two different sites in northern Norway (approx. 70°N and 23°E) in September 2017.
We combine offline ice nucleation experiments using the isostatic diffusion chamber FRankfurt
Ice Deposition FreezinG Experiment (FRIDGE) with offline single-particle electron microscopy
analysis for INP composition. We focus on INPs active at moderate subzero temperatures (>-
20°C) and differentiate between characteristics of INPs active above and below - 15°C. Most
particles that were analysed were of biological origin including particles lying in areas on the
sampling surface where ice was formed at - 20°C. This study can provide insight into typical
characteristics of biological INPs and helps to attribute sources of INPs active at relatively warm
temperatures.
REFERENCES 1 Pruppacher and Klett (1997), Microphysics of Clouds and Precipitation, 2nd ed., Kluwer Acad.,
Dordrecht, Netherlands. 2 Field et al. (2017), Chapter 7. Secondary Ice Production: Current state of the science and
recommendations for the future. Meteorol. Monogr., AMS MONOGRAPHS-D-16-0014.1. 3 Murray et al. (2012) Ice nucleation by particles immersed in supercooled cloud droplets.
Chemical Society Reviews 41, 6519-6554.
Significance of Fresh Water Ice Nucleating Particles in USA, UK and Mainland European Rivers
Moffett, B.F.1, DeMott2, P.J., Schmale3, D.G., Scheel4, J.F., Fröhlich-Nowoisky, J.4, McKay, R.M.5 and Hill,T.C.J.6
1Ocean Lab, Fishguard Harbour, Goodwick, Pembrokeshire SA64 0DE, United Kingdom 2Department of Atmospheric Science, Colorado State University, Fort Collins, CO 80523-
1371 3VirginiaTech, Department of Plant Pathology, Physiology, and Weed Science, 413 Price
Hall (0331), 170 Drillfield Drive, Blacksburg VA 24061-0331 4Max-Planck-Institut für Chemie, Hahn-Meitner-Weg 1, D-55128 Mainz, Germany
5Department of Biological Sciences, Bowling Green State University, Bowling Green, OH 43403
6Department of Atmospheric Science, Colorado State University, Fort Collins, CO 80523-1371
The nature of the ice nucleating particles (INP), which initiate precipitation, is still a matter of
debate. Most work on INPs has concentrated on bacteria such as Pseudomonas syringae and
other microbes including the fungus Mortierella alpine. Fresh water INP are now beginning
to be assessed as a potential source of atmospheric ice nuclei. Currently there are few
publications in this area. In this presentation I will demonstrate that INP are a ubiquitous
feature of all rivers analysed in Europe, UK and North America. The INP occur at numbers at
least 1000 times greater than in ocean water and the great majority are biogenic. As in the
oceans these INP are likely to be aerosolized by bubble bursting. Taking into account the
relative surface area of rivers compared to that of the oceans, the high numbers of INP in
fresh water may be more important to atmospheric processes than previously thought.
Using spectra characteristics to define ice nucleating particle populations from north and south of the Alps
Jessie M. Creamean1,2, Claudia Mignani3, Franz Conen3
1Cooperative Institute for Research in Environmental Sciences, University of Colorado, Boulder, CO, USA
2Physical Sciences Division, National Oceanic and Atmospheric Administration, Boulder, CO, USA
3Department of Environmental Sciences, University of Basel, Switzerland One of the least understood cloud processes is modulation of their microphysics by aerosols,
specifically of cloud ice by ice nucleating particles (INPs). To directly assess INP impacts on
cloud ice and subsequent precipitation formation, measurements in cloud environments are
necessary but difficult given the logistical challenges associated with airborne measurements
and separating interstitial aerosol from cloud residues. One solution is measurements at
mountaintop research stations which are commonly exposed to cloudy conditions. Here, we
present preliminary results from a comparison of INP spectral characteristics in air, cloud
rime, and fresh fallen snow for two winter storm cases at the High Altitude Research Station
Jungfraujoch. The goal of the study was two-fold: (1) to assess variability in wintertime INPs
based on storm direction and magnitude and (2) to evaluate INPs between different sampling
substances using normalized differential INP spectra. Both storms days were subject to strong
winds (average of 9 and up to 18 m s-1), in-cloud conditions, and snowfall. However,
temperatures were much warmer (−8 °C on average) as winds originated from the north
during the first storm day (15 Feb 2018) as compared to the southerly winds and colder
temperatures (−15°C on average) of the second storm day (23 Feb 2018). Such contrasting
meteorological conditions and aerosol sources led to disparate INP spectra from north to south
of Jungfraujoch and when comparing aerosol to cloud rime and snow samples. Evaluating
normalized differential INP spectra exhibited variable modality and shape—depending on the
types of INPs present—and may serve as a benchmark for comparing different sampling
substances.
Two totally different Arctic cirrus clouds in February - A case study
Veronika Wolf
Department of Computer Science, Electrical and Space Engineering, Lulea University of Technology, Kiruna, Sweden
[email protected] Cirrus clouds consist of ice crystals, which can have different shapes and sizes and vary in
number concentration. These diverse characteristics can lead to varying net cloud radiation.
For better weather and climate models and remote sensing retrieval, precise knowledge of
particle properties is required. For this purpose, balloon-borne in-situ measurements are
carried out in Kiruna, Sweden. The images obtained from the in-situ imager can be used to
determine particle properties such as size, shape, and number concentration.
Here two measurements are presented which reveal very different properties. On 20.2.2013 a
cirrus with many and very small particles has been measured. But on 12.2.2016 there was a
cirrus with very large and rather few particles. The shapes of the particles on the two days
were also totally different. On 20.2.2013 almost all particles were compact, but on 12.2.2016
most particles were irregular, rosettes or columns. That the particle properties of the two
clouds were so diverse was due to their origin. The particles on 20.2.2013 were formed
directly from the gas phase to the ice phase. By contrast, the particles have been generated via
the liquid phase on 12.2.2016.
Raindrop-freezing fragmentation in natural clouds
Vaughan Phillips
Lund University, Dept of Physical Geography and Ecosystem Science, Sölvegatan 12, S-223 62 Lund, Sweden
A numerical formulation is provided for secondary ice production during fragmentation of
freezing drops. This is obtained by pooling laboratory observations from past published
studies and by theoretically considering energy conservation of collisions. There are two
modes of the scheme: fragmentation of spherical freezing of raindrops, and that caused by
freezing in collisions with larger ice particles.
Microphysical simulations with a parcel model of fast ascent (8 m/sec) between -10° and -
20°C are validated against aircraft observations of tropical maritime deep convection. Ice
enhancement by an order of magnitude is predicted from inclusion of raindrop-freezing
fragmentation, as observed. The Hallett-Mossop (H-M) process was active too. Both
secondary ice mechanisms (H-M and raindrop-freezing) are accelerated by a positive
feedback with collisional raindrop-freezing.
An energy-based theory of the processes in a single drop is proposed explaining the lab
observations of fragment numbers depending on size and freezing temperature. To illustrate
the behaviour of the scheme, the glaciation of idealised monodisperse populations of drops is
elucidated with an analytical 0D theory treating the freezing in drop-ice collisions by a
positive feedback of fragmentation. When drops are too few or too small, especially at
temperatures far from -15°C, there is little ice multiplication on realistic time-scales of natural
clouds, but otherwise high ice enhancement (IE) ratios of up to 100-1000 are possible.
Theoretical formulae for glaciation times and growth rates and maximum IE ratios are
proposed.
Diurnal variation of cloud ice water path as observed from SAPHIR onboard Megha-Tropiques
Durgesh Piyush and Jayaraman Srinivasan
Divecha Centre for Climate Change, Indian Institute of Science, Bangalore, 560012, India [email protected]
Ice Water Path (IWP) plays a crucial role in determining the earth’s radiation budget. The
accurate measurement of ice water path is important in evaluating climate models. The
diurnal variations of ice water path are not known well due to inadequate temporal resolution
in polar orbiting satellites. SAPHIR (Sondeur Atmosphérique du Profil d’Humidité
Intertropicale par Radiométrie) onboard Megha-Tropiques (MT) with an inclination of 20
degree and swath of around 1700 km, provides observations 4 to 5 times a day for a given
location. In this study SAPHIR observations were used to find the diurnal variation of IWP. A
neural network based IWP retrieval algorithm was used to get the IWP from brightness
temperatures of SAPHIR. The diurnal amplitude, peak and mean of IWP for different regions
were calculated. Diurnal amplitude was found to be larger over land than over ocean. The
diurnal peak was observed in the evening over land, whereas it was in the morning over the
ocean. We have also used GPM-GMI derived IWP and SAPHIR derived deep convective
pixels to compare the diurnal variations. One year data of SAPHIR and GMI was used to
highlight the advantage to SAPHIR sampling in the diurnal variation study, the result shows
that average SAPHIR pixels per hour at any location is 5 to 7 times more than that of GMI.
Research Aircraft Observations of the Micro-physics of Ice Clouds
David J. Delene1, Nicholas J. Gapp1, Kurt Hibert2, and Dennis Afseth2
1University of North Dakota, Grand Forks, North Dakota, United States of America,
2Weather Modification International, Fargo, North Dakota, United States of America Research aircraft provide unique observations of the micro-physics of ice clouds. The
University of North Dakota (UND) has conducted airborne micro-physics research since the
1970’s using the Cessna Citation II twin-engine fanjet aircraft. The North Dakota Citation
Research Aircraft is now operated by Weather Modification International (WMI) of Fargo,
North Dakota. WMI and UND working together provide a platform capable of conducting a
wide range of field projects in a cost-effective manner, while providing a unique educational
experience for students. The Citation Research Aircraft has a number of design and
performance characteristics that make it an ideal platform for a wide range of atmospheric
studies, including sampling at high altitude (40,000 ft) which is critical for ice cloud
observations. WMI has the experience to install the custom scientific instrumentation required
for conducting in-situ observations of ice clouds, while UND provides the scientific
knowledge to obtain measurements that achieve the scientific objectives. Recent Citation
projects include the measurements of cirrus cloud particles in Florida thunderstorm anvils
during 2015 (CAPE2015 field project). During the CAPE2015 field project, ice particles were
sampled between an altitude of 29,000 ft and 40,000 ft on eight research flights. In-situ
observations were made using a Two-Dimensional Stereographic probe (2D-S) and a
Nevzorov Water Content Probe (Nevzorov). Remote sensing observations were made by the
United States Navy’s Mid-Course Radar (MCR). The MCR tracked the aircraft to obtain high
resolution radar reflectivity concurrent with in-situ probes. The concurrency of the
observations allows for examination of the variation of radar reflectivity that links cloud
micro-physics to the large-scale cloud structure and enables the understanding of cloud
evolution over time. A critical component to understanding cirrus clouds is robust software
that automates the processing of in-situ probe data. Correctly understanding and processing
two-dimensional cloud probe images to generate particle spectra is critical for comparison of
in-situ and remotely sensed data.
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