scholarly journals The Horizontal Ice Nucleation Chamber (HINC): INP measurements at conditions relevant for mixed-phase clouds at the High Altitude Research Station Jungfraujoch

2017 ◽  
Vol 17 (24) ◽  
pp. 15199-15224 ◽  
Author(s):  
Larissa Lacher ◽  
Ulrike Lohmann ◽  
Yvonne Boose ◽  
Assaf Zipori ◽  
Erik Herrmann ◽  
...  
Keyword(s):  
High Altitude ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
Saharan Dust ◽  
Research Station ◽  
Minimum Detectable Concentration ◽  
The North ◽  
New Instrument ◽  
Marine Air ◽  
Mixed Phase Clouds

Abstract. In this work we describe the Horizontal Ice Nucleation Chamber (HINC) as a new instrument to measure ambient ice-nucleating particle (INP) concentrations for conditions relevant to mixed-phase clouds. Laboratory verification and validation experiments confirm the accuracy of the thermodynamic conditions of temperature (T) and relative humidity (RH) in HINC with uncertainties in T of ±0.4 K and in RH with respect to water (RHw) of ±1.5 %, which translates into an uncertainty in RH with respect to ice (RHi) of ±3.0 % at T > 235 K. For further validation of HINC as a field instrument, two measurement campaigns were conducted in winters 2015 and 2016 at the High Altitude Research Station Jungfraujoch (JFJ; Switzerland, 3580 m a. s. l. ) to sample ambient INPs. During winters 2015 and 2016 the site encountered free-tropospheric conditions 92 and 79 % of the time, respectively. We measured INP concentrations at 242 K at water-subsaturated conditions (RHw = 94 %), relevant for the formation of ice clouds, and in the water-supersaturated regime (RHw = 104 %) to represent ice formation occurring under mixed-phase cloud conditions. In winters 2015 and 2016 the median INP concentrations at RHw = 94 % was below the minimum detectable concentration. At RHw = 104 %, INP concentrations were an order of magnitude higher, with median concentrations in winter 2015 of 2.8 per standard liter (std L−1; normalized to standard T of 273 K and pressure, p, of 1013 hPa) and 4.7 std L−1 in winter 2016. The measurements are in agreement with previous winter measurements obtained with the Portable Ice Nucleation Chamber (PINC) of 2.2 std L−1 at the same location. During winter 2015, two events caused the INP concentrations at RHw = 104 % to significantly increase above the campaign average. First, an increase to 72.1 std L−1 was measured during an event influenced by marine air, arriving at the JFJ from the North Sea and the Norwegian Sea. The contribution from anthropogenic or other sources can thereby not be ruled out. Second, INP concentrations up to 146.2 std L−1 were observed during a Saharan dust event. To our knowledge this is the first time that a clear enrichment in ambient INP concentration in remote regions of the atmosphere is observed during a time of marine air mass influence, suggesting the importance of marine particles on ice nucleation in the free troposphere.

scholarly journals The Horizontal Ice Nucleation Chamber HINC: INP measurements at Conditions Relevant for Mixed-Phase Clouds at the High Altitude Research Station Jungfraujoch

2017 ◽  
Author(s):  
Larissa Lacher ◽  
Ulrike Lohmann ◽  
Yvonne Boose ◽  
Assaf Zipori ◽  
Erik Herrmann ◽  
...  
Keyword(s):  
High Altitude ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
Saharan Dust ◽  
Research Station ◽  
Minimum Detectable Concentration ◽  
New Instrument ◽  
Order Of Magnitude ◽  
Marine Air ◽  
Mixed Phase Clouds

Abstract. In this work we describe the Horizontal Ice Nucleation Chamber, HINC as a new instrument to measure ambient ice nucleating particle (INP) concentrations for conditions relevant to mixed-phase clouds. Laboratory verification and validation experiments confirm accuracy of the thermodynamic conditions of temperature (T) and relative humidity (RH) in HINC with uncertainties in temperature of ±0.4 K and in RH with respect to water (RHw) of ±1.5 %, which translates to an uncertainty in RH with respect to ice (RHi) of ±3.0 % at T > 235 K. For further validation of HINC as a field instrument, two measurement campaigns were conducted in winters 2015 and 2016 at the High Altitude Research Station Jungfraujoch (JFJ; Switzerland, 3580 m a.s.l.) to sample ambient INPs. During winters 2015 and 2016 the site encountered free tropospheric conditions 92 % and 79 % of the time respectively. We measured INP concentrations at 242 K at water sub-saturated conditions (RHw = 94 %), relevant for the formation of ice clouds, and in the water supersaturated regime (RHw = 103–104 %) to represent ice formation occurring under mixed-phase cloud conditions. In winter 2015 and 2016 the median INP concentrations at RHw = 94 % was below the minimum detectable concentration. At RHw = 104 %, INP concentrations were an order of magnitude higher, with median concentrations in winter 2015 of 2.8 per standard liter (stdL−1; normalized to standard temperature T = 273 K and pressure p = 1013 hPa) and 4.7 stdL−1 in winter 2016. The measurements are in agreement with previous winter measurements obtained with the Portable Ice Nucleation Chamber, PINC, of 2.2 stdL−1 at the same location. During winter 2015, two events caused the INP concentrations at RHw = 103–104 % to significantly increase above the campaign average. First, an increase to 72.1 stdL−1 was measured during an event influenced by marine air, coming from the Northern Sea and the Norwegian Sea. Second, INP concentrations up to 146.2 stdL−1 were observed during a Saharan dust event. To our knowledge this is the first time that a clear enrichment in ambient INP concentration is observed during a time of marine air mass influence, indicating the importance of marine particles on ice nucleation in the free troposphere.

scholarly journals Impact of Air Mass Conditions and Aerosol Properties on Ice Nucleating Particle Concentrations at the High Altitude Research Station Jungfraujoch

Atmosphere ◽  
2018 ◽  
Vol 9 (9) ◽  
pp. 363 ◽  
Author(s):  
Larissa Lacher ◽  
Martin Steinbacher ◽  
Nicolas Bukowiecki ◽  
Erik Herrmann ◽  
Assaf Zipori ◽  
...  
Keyword(s):  
High Altitude ◽  
Correlation Coefficients ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
High Time Resolution ◽  
Research Station ◽  
Free Troposphere ◽  
Long Term Study ◽  
Mixed Phase Clouds ◽  
Aerosol Properties

Ice nucleation is the source of primary ice crystals in mixed-phase clouds. Only a small fraction of aerosols called ice nucleating particles (INPs) catalyze ice formation, with their nature and origin remaining unclear. In this study, we investigate potential predictor parameters of meteorological conditions and aerosol properties for INP concentrations at mixed-phase cloud condition at 242 K. Measurements were conducted at the High Altitude Research Station Jungfraujoch (Switzerland, 3580 m a.s.l.), which is located predominantly in the free troposphere (FT) but can occasionally receive injections from the boundary layer (BLI). Measurements are taken during a long-term study of eight field campaigns, allowing for the first time an interannual (2014–2017) and seasonal (spring, summer, and winter) distinction of high-time-resolution INP measurements. We investigate ranked correlation coefficients between INP concentrations and meteorological parameters and aerosol properties. While a commonly used parameterization lacks in predicting the observed INP concentrations, the best INP predictor is the total available surface area of the aerosol particles, with no obvious seasonal trend in the relationship. Nevertheless, the predicting capability is less pronounced in the FT, which might be caused by ageing effects. Furthermore, there is some evidence of anthropogenic influence on INP concentrations during BLI. Our study contributes to an improved understanding of ice nucleation in the free troposphere, however, it also underlines that a knowledge gap of ice nucleation in such an environment exists.

scholarly journals The effects of hygroscopicity on ice nucleation of fossil fuel combustion aerosols in mixed-phase clouds

2013 ◽  
Vol 13 (8) ◽  
pp. 4339-4348 ◽  
Author(s):  
Y. Yun ◽  
J. E. Penner ◽  
O. Popovicheva
Keyword(s):  
Fossil Fuel ◽  
Laboratory Data ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
Liquid Water Path ◽  
Anthropogenic Forcing ◽  
Soot Particles ◽  
Model Studies ◽  
Ability To Act ◽  
Mixed Phase Clouds

Abstract. Fossil fuel black carbon and organic matter (ffBC/OM) are often emitted together with sulfate, which coats the surface of these particles and changes their hygroscopicity. Observational studies at cirrus temperatures (≈−40 °C) show that the hygroscopicity of soot particles can modulate their ice nucleation ability. Here, we implement a scheme for 3 categories of soot (hydrophobic, hydrophilic and hygroscopic) on the basis of laboratory data and specify their ability to act as ice nuclei at mixed-phase temperatures by extrapolating the observations using a published deposition/condensation/immersion freezing parameterization. The new scheme results in significant changes to anthropogenic forcing in mixed-phase clouds. The net forcing in our offline model studies varies from 0.111 to 1.059 W m−2 depending on the ice nucleation capability of hygroscopic soot particles. The total anthropogenic cloud forcing and whole-sky forcing with the new scheme are 0.06 W m−2 and −2.45 W m−2, respectively, but could be more positive (by about 1.17 W m−2) if hygroscopic soot particles are allowed to nucleate ice particles. The change in liquid water path dominates the anthropogenic forcing in mixed-phase clouds.

Source identification of aerosol chemical composition in the Atlas region of North Africa.

2021 ◽  
Author(s):  
Nabil Deabji ◽  
Khanneh Wadinga Fomba ◽  
Eduardo José dos Santos Souza ◽  
Hartmut Herrmann
Keyword(s):  
High Altitude ◽  
Complex Mixture ◽  
Saharan Dust ◽  
Atmospheric Composition ◽  
Urban Site ◽  
Chemical Components ◽  
Research Station ◽  
African Region ◽  
Aerosol Composition ◽  
The Impact

<p>Aerosol particles are important constituents of the atmosphere due to their role in controlling climate-related processes. In addition, their impacts on air quality and human health make it essential to study. However, the characterization and the identification of natural and anthropogenic atmospheric particles can be challenging due to the complex mixture occurring during atmospheric transport. Background locations such as high-altitude sites provide valuable infrastructure for obtaining representative data for understanding various pathways for aerosol interactions useful in assessing atmospheric composition. However, information about aerosol characteristics at high-altitude in the African regions and their relation to urban aerosol composition is still not well understood. In the present study, PM<sub>10</sub> and PM<sub>2.5</sub> particulate matter was characterized at two different sites in the North African region of Morocco. A background site located at the newly established AM5 research station in the Middle Atlas region at an altitude of 2100 m and an urban site situated in a polluted city, Fez. The goal was to determine chemical components, evaluate Saharan dust’s role on the PM10 concentrations between the sites, and assess the impact of urban pollution on background aerosol composition. The results indicate that the background aerosol composition is influenced by both regional and trans-regional transport. Despite the site's proximity to the Sahara Desert, the deserts influence on the atmospheric composition was observed for only 22% of the time and this was mainly seasonal. Marine air masses were more dominant with a mixture of sea salt and polluted aerosol from the coastal regions especially during wintertime. Furthermore, high concentrations of mineral dust were observed during the daytime due to the resuspension of road dust. At the same time, an increase of PAHs and anthropogenic metals such as Pb, Ni, and Cu were found during the nighttime because of the boundary layer variation. The Fez's urban site is characterized by a high contribution of elemental carbon (6%) and organic biomass tracers (3%) such as Levoglucosane and 4-nitrophenol.</p>

Towards a molecular-based parameterization of the ice nucleation activity of biological macromolecules and its implications for aerosol-cloud interactions

2021 ◽  
Author(s):  
Minghui Zhang ◽  
Amina Khaled ◽  
Pierre Amato ◽  
Anne-Marie Delort ◽  
Barbara Ervens
Keyword(s):  
Fungal Spores ◽  
Chemical Properties ◽  
Active Surface ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
Biological Macromolecules ◽  
Cloud Properties ◽  
Nucleation Activity ◽  
Mixed Phase Clouds ◽  
Ice Nucleation Activity

<p>Primary biological aerosol particles (PBAPs) play an important role in mixed-phase clouds as they nucleate ice even at temperatures of T > -10 °C. Current parameterizations of PBAP ice nucleation are based on ice nucleation active surface site (INAS) densities that are derived from freezing experiments. However, only a small fraction of the PBAP surface is responsible for their ice nucleation activity, such as proteins of bacteria cells, fungal spores, pollen polysaccharides and other (unidentified) macromolecules. Based on literature data, we refine the INAS density parameterizations by further parameters:</p><p>1) We demonstrate that the ice nucleation activity of such individual macromolecules is much higher than that of PBAPs. It can be shown that INAS of PBAPs can be scaled by the surface fraction of these ice-nucleating molecules.</p><p>2) Previous studies suggested that ice nucleation activity tends to be higher for larger macromolecules and their aggregates. We show that these trends hold true for various groups of macromolecules that comprise PBAPs.</p><p>Based on these trends, we suggest a more refined parameterization for ice-nucleating macromolecules in different types of PBAPs and even for different species of bacteria, fungi, and pollen. This new parameterization can be considered a step towards a molecular-based approach to predict the ice nucleation activity of the macromolecules in PBAPs based on their biological and chemical properties.</p><p>We implement both the traditional INAS parameterization for complete PBAPs and our parameterization for individual molecules in an adiabatic cloud parcel model. The extent will be discussed to which the two parameterizations result in different cloud properties of mixed-phase clouds.</p>

scholarly journals Chemical composition and mixing-state of ice residuals sampled within mixed phase clouds

2011 ◽  
Vol 11 (6) ◽  
pp. 2805-2816 ◽  
Author(s):  
M. Ebert ◽  
A. Worringen ◽  
N. Benker ◽  
S. Mertes ◽  
E. Weingartner ◽  
...  
Keyword(s):  
Chemical Composition ◽  
Carbonaceous Material ◽  
Mixed Phase ◽  
Research Station ◽  
Mixing State ◽  
Anthropogenic Component ◽  
Significant Enrichment ◽  
Alpine Research ◽  
Main Component ◽  
Mixed Phase Clouds

Abstract. During an intensive campaign at the high alpine research station Jungfraujoch, Switzerland, in February/March 2006 ice particle residuals within mixed-phase clouds were sampled using the Ice-counterflow virtual impactor (Ice-CVI). Size, morphology, chemical composition, mineralogy and mixing state of the ice residual and the interstitial (i.e., non-activated) aerosol particles were analyzed by scanning and transmission electron microscopy. Ice nuclei (IN) were identified from the significant enrichment of particle groups in the ice residual (IR) samples relative to the interstitial aerosol. In terms of number lead-bearing particles are enriched by a factor of approximately 25, complex internal mixtures with silicates or metal oxides as major components by a factor of 11, and mixtures of secondary aerosol and carbonaceous material (C-O-S particles) by a factor of 2. Other particle groups (sulfates, sea salt, Ca-rich particles, external silicates) observed in the ice-residual samples cannot be assigned unambiguously as IN. Between 9 and 24% of all IR are Pb-bearing particles. Pb was found as major component in around 10% of these particles (PbO, PbCl2). In the other particles, Pb was found as some 100 nm sized agglomerates consisting of 3–8 nm sized primary particles (PbS, elemental Pb). C-O-S particles are present in the IR at an abundance of 17–27%. The soot component within these particles is strongly aged. Complex internal mixtures occur in the IR at an abundance of 9–15%. Most IN identified at the Jungfraujoch station are internal mixtures containing anthropogenic components (either as main or minor constituent), and it is concluded that admixture of the anthropogenic component is responsible for the increased IN efficiency within mixed phase clouds. The mixing state appears to be a key parameter for the ice nucleation behaviour that cannot be predicted from the sole knowledge of the main component of an individual particle.

scholarly journals Contribution of feldspar and marine organic aerosols to global ice nucleating particle concentrations

2017 ◽  
Vol 17 (5) ◽  
pp. 3637-3658 ◽  
Author(s):  
Jesús Vergara-Temprado ◽  
Benjamin J. Murray ◽  
Theodore W. Wilson ◽  
Daniel O'Sullivan ◽  
Jo Browse ◽  
...  
Keyword(s):  
Regional Distribution ◽  
Organic Aerosols ◽  
Field Measurements ◽  
Field Work ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
Aerosol Composition ◽  
Desert Dust ◽  
Concentration Changes ◽  
Mixed Phase Clouds

Abstract. Ice-nucleating particles (INPs) are known to affect the amount of ice in mixed-phase clouds, thereby influencing many of their properties. The atmospheric INP concentration changes by orders of magnitude from terrestrial to marine environments, which typically contain much lower concentrations. Many modelling studies use parameterizations for heterogeneous ice nucleation and cloud ice processes that do not account for this difference because they were developed based on INP measurements made predominantly in terrestrial environments without considering the aerosol composition. Errors in the assumed INP concentration will influence the simulated amount of ice in mixed-phase clouds, leading to errors in top-of-atmosphere radiative flux and ultimately the climate sensitivity of the model. Here we develop a global model of INP concentrations relevant for mixed-phase clouds based on laboratory and field measurements of ice nucleation by K-feldspar (an ice-active component of desert dust) and marine organic aerosols (from sea spray). The simulated global distribution of INP concentrations based on these two species agrees much better with currently available ambient measurements than when INP concentrations are assumed to depend only on temperature or particle size. Underestimation of INP concentrations in some terrestrial locations may be due to the neglect of INPs from other terrestrial sources. Our model indicates that, on a monthly average basis, desert dusts dominate the contribution to the INP population over much of the world, but marine organics become increasingly important over remote oceans and they dominate over the Southern Ocean. However, day-to-day variability is important. Because desert dust aerosol tends to be sporadic, marine organic aerosols dominate the INP population on many days per month over much of the mid- and high-latitude Northern Hemisphere. This study advances our understanding of which aerosol species need to be included in order to adequately describe the global and regional distribution of INPs in models, which will guide ice nucleation researchers on where to focus future laboratory and field work.

scholarly journals Possible roles of ice nucleation mode and ice nuclei depletion in the extended lifetime of Arctic mixed-phase clouds

2005 ◽  
Vol 32 (18) ◽  
pp. n/a-n/a ◽  
Author(s):  
Hugh Morrison ◽  
Matthew D. Shupe ◽  
James O. Pinto ◽  
Judith A. Curry
Keyword(s):  
Ice Nucleation ◽  
Mixed Phase ◽  
Nucleation Mode ◽  
Ice Nuclei ◽  
Mixed Phase Clouds

scholarly journals The efficiency of secondary organic aerosol particles to act as ice nucleating particles at mixed-phase cloud conditions

2018 ◽  
Author(s):  
Wiebke Frey ◽  
Dawei Hu ◽  
James Dorsey ◽  
M. Rami Alfarra ◽  
Aki Pajunoja ◽  
...  
Keyword(s):  
Secondary Organic Aerosol ◽  
Aerosol Particles ◽  
Organic Aerosol ◽  
Ice Nucleation ◽  
Mixed Phase ◽  
Dust Particles ◽  
Ice Cloud ◽  
Liquid Saturation ◽  
Reference Experiment ◽  
Mixed Phase Clouds

Abstract. Secondary Organic Aerosol (SOA) particles have been found to be efficient ice nucleating particles under the cold conditions of (tropical) upper tropospheric cirrus clouds. Whether they also are efficient at initiating freezing at slightly warmer conditions as found in mixed phase clouds remains undetermined. Here, we study the ice nucleating ability of photo-chemically produced SOA particles with the combination of the Manchester Aerosol and Ice Cloud Chambers. Three SOA systems were tested resembling biogenic/anthropogenic particles and particles of different phase state. After the aerosol particles were formed, they were transferred into the cloud chamber where subsequent quasi-adiabatic cloud evacuations were performed. Additionally, the ice forming abilities of ammonium sulfate and kaolinite were investigated as a reference to test the experimental setup. Clouds were formed in the temperature range of −20 °C to −28.6 °C. Only the reference experiment using dust particles showed evidence of ice nucleation. No ice particles were observed in any other experiment. Thus, we conclude that SOA particles produced under the conditions of the reported experiments are not efficient ice nucleating particles starting at liquid saturation under mixed-phase cloud conditions.

Sign in / Sign up

Export Citation Format

Share Document