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
2010 ◽  
Vol 10 (18) ◽  
pp. 8649-8667 ◽  
Author(s):  
A. Wiacek ◽  
T. Peter ◽  
U. Lohmann

Abstract. This modelling study explores the availability of mineral dust particles as ice nuclei for interactions with ice, mixed-phase and liquid water clouds, also tracking the particles' history of cloud-processing. We performed 61 320 one-week forward trajectory calculations originating near the surface of major dust emitting regions in Africa and Asia using high-resolution meteorological analysis fields for the year 2007. Dust-bearing trajectories were assumed to be those coinciding with known dust emission seasons, without explicitly modelling dust emission and deposition processes. We found that dust emissions from Asian deserts lead to a higher potential for interactions with high ice clouds, despite being the climatologically much smaller dust emission source. This is due to Asian regions experiencing significantly more ascent than African regions, with strongest ascent in the Asian Taklimakan desert at ~25%, ~40% and 10% of trajectories ascending to 300 hPa in spring, summer and fall, respectively. The specific humidity at each trajectory's starting point was transported in a Lagrangian manner and relative humidities with respect to water and ice were calculated in 6-h steps downstream, allowing us to estimate the formation of liquid, mixed-phase and ice clouds. Downstream of the investigated dust sources, practically none of the simulated air parcels reached conditions of homogeneous ice nucleation (T≲−40 °C) along trajectories that have not experienced water saturation first. By far the largest fraction of cloud forming trajectories entered conditions of mixed-phase clouds, where mineral dust will potentially exert the biggest influence. The majority of trajectories also passed through atmospheric regions supersaturated with respect to ice but subsaturated with respect to water, where so-called "warm ice clouds" (T≳−40 °C) theoretically may form prior to supercooled water or mixed-phase clouds. The importance of "warm ice clouds" and the general influence of dust in the mixed-phase cloud region are highly uncertain due to both a considerable scatter in recent laboratory data from ice nucleation experiments, which we briefly review in this work, and due to uncertainties in sub-grid scale vertical transport processes unresolved by the present trajectory analysis. For "classical" cirrus-forming temperatures (T≲−40 °C), our results show that only mineral dust ice nuclei that underwent mixed-phase cloud-processing, most likely acquiring coatings of organic or inorganic material, are likely to be relevant. While the potential paucity of deposition ice nuclei shown in this work dimishes the possibility of deposition nucleation, the absence of liquid water droplets at T≲−40 °C makes the less explored contact freezing mechanism (involving droplet collisions with bare ice nuclei) highly inefficient. These factors together indicate the necessity of further systematic studies of immersion mode ice nucleation on mineral dust suspended in atmospherically relevant coatings.


2012 ◽  
Vol 12 (8) ◽  
pp. 19987-20006
Author(s):  
Y. Yun ◽  
J. E. Penner ◽  
O. Popovicheva

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 show that the hygroscopicity of soot particles can modulate their ice nucleation ability. To address this, we implemented a scheme that uses 3 levels of soot hygroscopicity (hydrophobic, hydrophilic and hygroscopic) and used laboratory data to specify their ice nuclei abilities. The new scheme results in significant changes to anthropogenic forcing in mixed-phase clouds. The net forcing in off-line 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 is 0.06 W m−2 and −2.45 W m−2, respectively, but could be more positive if hygroscopic soot particles are allowed to nucleate ice particles. The change in liquid water path dominates the anthropogenic forcing in mixed-phase clouds.


2014 ◽  
Vol 14 (4) ◽  
pp. 5013-5059 ◽  
Author(s):  
D. I. Haga ◽  
S. M. Burrows ◽  
R. Iannone ◽  
M. J. Wheeler ◽  
R. Mason ◽  
...  

Abstract. Ice nucleation on fungal spores may affect the frequency and properties of ice and mixed-phase clouds. We studied the ice nucleation properties of 12 different species of fungal spores chosen from three classes: Agaricomycetes, Ustilaginomycetes, and Eurotiomycetes. Agaricomycetes include many types of mushroom species and are cosmopolitan. Ustilaginomycetes are agricultural pathogens and have caused widespread damage to crops. Eurotiomycetes are found on all types of decaying material and include important human allergens. We focused on these classes since they are thought to be abundant in the atmosphere and because there is very little information on the ice nucleation ability of these classes of spores in the literature. All of the fungal spores investigated were found to cause freezing of water droplets at temperatures warmer than homogeneous freezing. The cumulative number of ice nuclei per spore was 0.001 at temperatures between −19 °C and −29 °C, 0.01 between −25.5 °C and −31 °C, and 0.1 between −26 °C and −36 °C. On average, the order of ice nucleating ability for these spores is Ustilaginomycetes > Agaricomycetes ≃ Eurotiomycetes. We show that at temperatures below −20 °C, all of the fungal spores studied here are less efficient ice nuclei compared to Asian mineral dust on a per surface area basis. We used our new freezing results together with data in the literature to compare the freezing temperatures of spores from the phyla Basidiomycota and Ascomycota, which together make up 98% of known fungal species found on Earth. The data show that within both phyla (Ascomycota and Basidiomycota) there is a wide range of freezing properties, and also that the variation within a phylum is greater than the variation between the average freezing properties of the phyla. Using a global chemistry–climate transport model, we investigated whether ice nucleation on the studied spores, followed by precipitation, can influence the atmospheric transport and global distributions of these spores in the atmosphere. Simulations show that inclusion of ice nucleation scavenging of these fungal spores in mixed-phase clouds can decrease the annual mean concentrations of fungal spores in near-surface air over the oceans and polar regions and decrease annual mean mixing ratios in the upper troposphere.


Author(s):  
Jaakko Ahola ◽  
Hannele Korhonen ◽  
Juha Tonttila ◽  
Sami Romakkaniemi ◽  
Harri Kokkola ◽  
...  

<p>We have extended the large-eddy model UCLALES-SALSA (Tonttila et al., 2017) to include formation of ice and mixed-phase clouds. The model has exceptionally detailed aerosol description for both aerosol number and chemical composition. We confirmed the accuracy of newly implemented ice microphysics with a comparison to a previous mixed-phase cloud model intercomparison study.</p><p>In a further simulation the model captured the typical layered structure of Arctic mixed-phase clouds: a liquid layer near cloud top and ice within and below the liquid layer. The simulation also demonstrated how larger droplets froze first. Moreover, the simulation showed realistic freezing rates of droplets within the vertical cloud structure. These characteristics were possible to capture with a heterogeneous ice nucleation scheme, where also ice nucleating particles (INP) are prognosed. Here, dust containing particles acted as INPs.</p><p>The prognostic simulation showed the importance of the self-adjustment of ice nucleation active particles. This is in good agreement with an observational study where resilient mixed-phase clouds are seen together with relatively high ice nuclei concentrations.</p><p>The implemented detailed sectional ice microphysics with prognostic aerosols is essentially important in reproducing the characteristics of mixed-phase clouds. The manuscript of this study is submitted for publication.</p>


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.


2013 ◽  
Vol 13 (8) ◽  
pp. 4339-4348 ◽  
Author(s):  
Y. Yun ◽  
J. E. Penner ◽  
O. Popovicheva

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.


2021 ◽  
Author(s):  
Minghui Zhang ◽  
Amina Khaled ◽  
Pierre Amato ◽  
Anne-Marie Delort ◽  
Barbara Ervens

<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>


2017 ◽  
Vol 17 (24) ◽  
pp. 15199-15224 ◽  
Author(s):  
Larissa Lacher ◽  
Ulrike Lohmann ◽  
Yvonne Boose ◽  
Assaf Zipori ◽  
Erik Herrmann ◽  
...  

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.


2017 ◽  
Vol 17 (5) ◽  
pp. 3637-3658 ◽  
Author(s):  
Jesús Vergara-Temprado ◽  
Benjamin J. Murray ◽  
Theodore W. Wilson ◽  
Daniel O'Sullivan ◽  
Jo Browse ◽  
...  

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.


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