STRATOSPHERIC ICE NUCLEI

1961 ◽  
Vol 18 (6) ◽  
pp. 804-806 ◽  
Author(s):  
E. K. Bigg ◽  
G. T. Miles ◽  
K. J. Heffernan
Keyword(s):  
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Slobodan Nickovic ◽  
Bojan Cvetkovic ◽  
Slavko Petković ◽  
Vassilis Amiridis ◽  
Goran Pejanović ◽  
...  

AbstractIce particles in high-altitude cold clouds can obstruct aircraft functioning. Over the last 20 years, there have been more than 150 recorded cases with engine power-loss and damage caused by tiny cloud ice crystals, which are difficult to detect with aircraft radars. Herein, we examine two aircraft accidents for which icing linked to convective weather conditions has been officially reported as the most likely reason for catastrophic consequences. We analyze whether desert mineral dust, known to be very efficient ice nuclei and present along both aircraft routes, could further augment the icing process. Using numerical simulations performed by a coupled atmosphere-dust model with an included parameterization for ice nucleation triggered by dust aerosols, we show that the predicted ice particle number sharply increases at approximate locations and times of accidents where desert dust was brought by convective circulation to the upper troposphere. We propose a new icing parameter which, unlike existing icing indices, for the first time includes in its calculation the predicted dust concentration. This study opens up the opportunity to use integrated atmospheric-dust forecasts as warnings for ice formation enhanced by mineral dust presence.


1969 ◽  
Vol 26 (6) ◽  
pp. 1342-1343 ◽  
Author(s):  
A. H. Auer ◽  
D. L. Veal ◽  
J. D. Marwitz
Keyword(s):  

Nature ◽  
1966 ◽  
Vol 212 (5060) ◽  
pp. 384-385 ◽  
Author(s):  
GABOR VALI
Keyword(s):  

2013 ◽  
Vol 71 (1) ◽  
pp. 89-97 ◽  
Author(s):  
Gianni Santachiara ◽  
Franco Belosi ◽  
Franco Prodi

Abstract This paper addresses the problem of the large discrepancies between ice crystal concentrations in clouds and the number of ice nuclei in nearby clear air reported in published papers. Such discrepancies cannot always be explained, even by taking into account both primary and secondary ice formation processes. A laboratory experiment was performed in a cylindrical column placed in a cold room at atmospheric pressure and temperature in the −12° to −14°C range. Supercooled droplets were nucleated in the column, in the absence of aerosol ice nuclei, by injecting ice crystals generated outside in a small syringe. A rapid increase in the ice crystal concentration was observed in the absence of any known ice multiplication. The ratio between the mean number of ice crystals in the column, after complete droplet vaporization, and the number of ice crystals introduced in the column was about 10:1. The presence of small ice crystals (introduced at the top of the column) in the unstable system (supercooled droplets) appears to trigger the transformation in the whole supercooled liquid cloud. A possible explanation could be that the rapidly evaporating droplets cool sufficiently to determine a homogeneous nucleation.


2017 ◽  
Vol 200 ◽  
pp. 165-194 ◽  
Author(s):  
Joseph C. Charnawskas ◽  
Peter A. Alpert ◽  
Andrew T. Lambe ◽  
Thomas Berkemeier ◽  
Rachel E. O’Brien ◽  
...  

Anthropogenic and biogenic gas emissions contribute to the formation of secondary organic aerosol (SOA). When present, soot particles from fossil fuel combustion can acquire a coating of SOA. We investigate SOA–soot biogenic–anthropogenic interactions and their impact on ice nucleation in relation to the particles’ organic phase state. SOA particles were generated from the OH oxidation of naphthalene, α-pinene, longifolene, or isoprene, with or without the presence of sulfate or soot particles. Corresponding particle glass transition (Tg) and full deliquescence relative humidity (FDRH) were estimated using a numerical diffusion model. Longifolene SOA particles are solid-like and all biogenic SOA sulfate mixtures exhibit a core–shell configuration (i.e.a sulfate-rich core coated with SOA). Biogenic SOA with or without sulfate formed ice at conditions expected for homogeneous ice nucleation, in agreement with respectiveTgand FDRH. α-pinene SOA coated soot particles nucleated ice above the homogeneous freezing temperature with soot acting as ice nuclei (IN). At lower temperatures the α-pinene SOA coating can be semisolid, inducing ice nucleation. Naphthalene SOA coated soot particles acted as ice nuclei above and below the homogeneous freezing limit, which can be explained by the presence of a highly viscous SOA phase. Our results suggest that biogenic SOA does not play a significant role in mixed-phase cloud formation and the presence of sulfate renders this even less likely. However, anthropogenic SOA may have an enhancing effect on cloud glaciation under mixed-phase and cirrus cloud conditions compared to biogenic SOA that dominate during pre-industrial times or in pristine areas.


2006 ◽  
Vol 6 (1) ◽  
pp. 67-80 ◽  
Author(s):  
A. Teller ◽  
Z. Levin

Abstract. Numerical experiments were carried out using the Tel-Aviv University 2-D cloud model to investigate the effects of increased concentrations of Cloud Condensation Nuclei (CCN), giant CCN (GCCN) and Ice Nuclei (IN) on the development of precipitation and cloud structure in mixed-phase sub-tropical convective clouds. In order to differentiate between the contribution of the aerosols and the meteorology, all simulations were conducted with the same meteorological conditions. The results show that under the same meteorological conditions, polluted clouds (with high CCN concentrations) produce less precipitation than clean clouds (with low CCN concentrations), the initiation of precipitation is delayed and the lifetimes of the clouds are longer. GCCN enhance the total precipitation on the ground in polluted clouds but they have no noticeable effect on cleaner clouds. The increased rainfall due to GCCN is mainly a result of the increased graupel mass in the cloud, but it only partially offsets the decrease in rainfall due to pollution (increased CCN). The addition of more effective IN, such as mineral dust particles, reduces the total amount of precipitation on the ground. This reduction is more pronounced in clean clouds than in polluted ones. Polluted clouds reach higher altitudes and are wider than clean clouds and both produce wider clouds (anvils) when more IN are introduced. Since under the same vertical sounding the polluted clouds produce less rain, more water vapor is left aloft after the rain stops. In our simulations about 3.5 times more water evaporates after the rain stops from the polluted cloud as compared to the clean cloud. The implication is that much more water vapor is transported from lower levels to the mid troposphere under polluted conditions, something that should be considered in climate models.


1994 ◽  
Vol 98 (15) ◽  
pp. 4087-4093 ◽  
Author(s):  
J. Majewski ◽  
R. Popovitz-Biro ◽  
K. Kjaer ◽  
J. Als-Nielsen ◽  
M. Lahav ◽  
...  

2017 ◽  
Author(s):  
Federico Carotenuto ◽  
Teodoro Georgiadis ◽  
Beniamino Gioli ◽  
Christel Leyronas ◽  
Cindy E. Morris ◽  
...  

Abstract. Microbial aerosols (mainly composed by bacterial and fungal cells), may constitute up to 74 % of the total aerosol volume. These biological aerosols are relevant not only from the point of view of the dispersion of pathogenic species, but also due to the potential geochemical implications. Some bacteria and fungi may, in fact, serve as cloud condensation or ice nuclei, potentially affecting cloud formation and precipitation and are active at higher temperatures compared to their, much more intensively studied, inorganic counterparts. Simulations of the impact of microbial aerosols on climate are still hindered by the lack of information regarding their emissions from ground sources. This work tackles this knowledge gap by (i) applying a rigorous micrometeorological approach to the estimation of microbial net fluxes above a Mediterranean grassland and (ii) developing a deterministic model to estimate these emissions on the basis of a few easily recovered meteorological parameters (the PLAnET model). The grassland itself is characterized by an abundance of positive net microbial fluxes and the model proves to be a promising tool capable of capturing the day-to-day variability in microbial fluxes with a relatively small bias and sufficient accuracy. PLAnET is still in its infancy and will benefit from future campaigns extending the available training dataset as well as the inclusion of ever more complex and critical phenomena affecting the release of microbial aerosol (such as rainfall). The model itself is also adaptable as an emission module for dispersion and chemical transport models, allowing to further explore the impact of microbial aerosols on the atmosphere and climate.


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