Size-Resolved Surface-Active Substances of Atmospheric Aerosol: Reconsideration of the Impact on Cloud Droplet Formation

2018 ◽  
Vol 52 (16) ◽  
pp. 9179-9187 ◽  
Author(s):  
Ana Kroflič ◽  
Sanja Frka ◽  
Martin Simmel ◽  
Heike Wex ◽  
Irena Grgić
2009 ◽  
Vol 6 (28) ◽  
pp. 282024
Author(s):  
Noenne Lvng Prisle ◽  
T Raatikainen ◽  
A Laaksonen ◽  
M Bilde

2020 ◽  
Author(s):  
Craig Poku ◽  
Andrew N. Ross ◽  
Adrian A. Hill ◽  
Alan M. Blyth ◽  
Ben Shipway

Abstract. Aerosols play a crucial role in the fog life cycle, as they determine the droplet number concentration, and hence droplet size, which in turn controls both the fog's optical thickness and life span. Detailed aerosol-microphysics schemes which accurately represent droplet formation and growth are unsuitable for weather forecasting and climate models, as the computational power required to calculate droplet formation would dominate the treatment of the rest of the physics in the model. A simple method to account for droplet formation is the use of an aerosol activation scheme, which parameterises the droplet number concentration based on a change in supersaturation at a given time. Traditionally, aerosol activation parameterisation schemes were designed for convective clouds and assume that supersaturation is reached through adiabatic lifting, with many imposing a minimum vertical velocity (e.g. 0.1 m/s) to account for unresolved sub-grid ascent. In radiation fog, the measured updrafts during initial formation are often insignificant, with radiative cooling being the dominant process leading to saturation. As a result, there is a risk that many aerosol activation schemes will overpredict the initial fog number concentration, which in turn may result in the fog transitioning to an optically thick layer too rapidly. This paper presents a more physically-based aerosol activation scheme that can account for a change in saturation due to non-adiabatic processes. Using an offline model, our results show that the minimum updraft velocity threshold assumption can overpredict the droplet number by up to 70 % in comparison to a cooling rate found in fog formation. The new scheme has been implemented in the Met Office Natural Environment Research Council (NERC) Cloud (MONC) LES model, and tested using observations of a radiation fog case study based in Cardington, UK. The results in this work show that using a more physically-based method of aerosol activation leads to the calculation of a more appropriate cloud droplet number. As a result, there is a slower transition to an optically thick (well-mixed) fog that is more in-line with observations. The results shown in this paper demonstrate the importance of aerosol activation representation in fog modelling, and the impact that the cloud droplet number has on processes linked to the formation and development of radiation fog. Unlike the previous parameterisation for aerosol activation, the revised scheme is suitable to simulate aerosol activation in both fog and convective cloud regimes.


2010 ◽  
Vol 10 (10) ◽  
pp. 23601-23625
Author(s):  
N. L. Prisle ◽  
M. Dal Maso ◽  
H. Kokkola

Abstract. Atmospheric aerosols often contain surface active organics. Surface activity can affect cloud droplet formation through both surface partitioning and surface tension reduction in activating droplets. However, a comprehensive thermodynamic account for these effects in Köhler modeling is computationally demanding and requires knowledge of both droplet composition and component molecular properties, which is generally unavailable. Here, a simple representation of activation properties for surface active organics is introduced and compared against detailed model predictions and laboratory measurements of CCN activity for mixed surfactant-salt particles from the literature. This simple organic representation is seen to work well for aerosol organic-inorganic composition ranges typically found in the atmosphere, and agreement with both experiments and detailed model predictions increases with surfactant strength. The simple representation does not require resolution of the organic aerosol composition and relies solely on properties of the organic fraction that can be measured directly with available techniques. Thus, it has high potential for application to complex and ambient aerosol. It is not computationally demanding, and therefore also has potential for implementation to atmospheric models accounting for cloud microphysics.


Tellus B ◽  
2012 ◽  
Vol 64 (1) ◽  
pp. 18490 ◽  
Author(s):  
S. Frka ◽  
J. Dautović ◽  
Z. Kozarac ◽  
B. Ćosović ◽  
A. Hoffer ◽  
...  

2011 ◽  
Vol 11 (9) ◽  
pp. 4073-4083 ◽  
Author(s):  
N. L. Prisle ◽  
M. Dal Maso ◽  
H. Kokkola

Abstract. Atmospheric aerosols often contain surface active organics. Surface activity can affect cloud droplet formation through both surface partitioning and surface tension reduction in activating droplets. However, a comprehensive thermodynamic account for these effects in Köhler modeling is computationally demanding and requires knowledge of both droplet composition and component molecular properties, which is generally unavailable. Here, a simple representation of activation properties for surface active organics is introduced and compared against detailed model predictions and laboratory measurements of CCN activity for mixed surfactant-salt particles from the literature. This simple organic representation is seen to work well for aerosol organic-inorganic composition ranges typically found in the atmosphere, and agreement with both experiments and detailed model predictions increases with surfactant strength. The simple representation does not require resolution of the organic aerosol composition and relies solely on properties of the organic fraction that can be measured directly with available techniques. It can thus potentially be applied to complex and ambient surface active aerosols. It is not computationally demanding, and therefore has high potential for implementation to atmospheric models accounting for cloud microphysics.


2016 ◽  
Author(s):  
Vlassis A. Karydis ◽  
Alexandra P. Tsimpidi ◽  
Sara Bacer ◽  
Andrea Pozzer ◽  
Athanasios Nenes ◽  
...  

Abstract. The importance of wind-blown mineral dust for cloud droplet formation is studied by considering i) the adsorption of water on the surface of insoluble particles, ii) the particle coating by soluble material (due to atmospheric aging) which augments cloud condensation nuclei (CCN) activity, and iii) the effect of dust on inorganic aerosol concentrations through thermodynamic interactions with mineral cations. The ECHAM5/MESSy Atmospheric Chemistry (EMAC) model is used to simulate the composition of global atmospheric aerosol; the ISORROPIA-II thermodynamic equilibrium model treats the interactions of K+-Ca2+-Mg2+-NH4+-Na+-SO42−-NO3−-Cl−-H2O aerosol with gas-phase inorganic constituents. Dust is considered a mixture of inert material with reactive minerals; emissions are calculated online by taking into account the soil particle size distribution and chemical composition of different deserts worldwide. The impact of dust on droplet formation is treated through the "unified dust activation parameterization" that considers the inherent hydrophilicity from adsorption and acquired hygroscopicity from soluble salts during aging. Our simulations suggest that the presence of dust increases cloud droplet number concentrations (CDNC) over major deserts (e.g., up to 20 % over the Sahara and Taklimakan Deserts) and decreases CDNC over polluted areas (e.g., up to 10 % over southern Europe and 20 % over northeastern Asia). This leads to a global net decrease of CDNC by 11 %. The adsorption activation of insoluble aerosols and the mineral dust chemistry are shown to be equally important for the cloud droplet formation over the main desserts, e.g., by considering these effects CDNC increases by 20 % over the Sahara. Remote from deserts the application of adsorption theory is critically important since the increased water uptake by the large aged dust particles (i.e., due to the added hydrophilicity by the soluble coating) reduce the maximum supersaturation and thus the cloud droplet formation from the smaller anthropogenic particles (e.g., CDNC decreases by 10 % over southern Europe and 20 % over northeastern Asia by applying adsorption theory). The global average CDNC decreases by 10 % by considering adsorption activation, while changes are negligible when accounting for the mineral dust chemistry. Sensitivity simulations indicate that CDNC is also sensitive to the mineral dust mass and inherent hydrophilicity, and not to the chemical composition of the emitted dust.


Author(s):  
Suleiman G. O Gakhramanov ◽  
◽  
Olga N. Torgashkova ◽  
Alexander. S. Belikov ◽  
Eugenia N. Nikiforova ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document