Measurements of Saharan Dust in Convective Clouds over the Tropical Eastern Atlantic Ocean*

2015 ◽  
Vol 72 (1) ◽  
pp. 75-81 ◽  
Author(s):  
Cynthia H. Twohy

Abstract Mineral dust particles have been shown to act as cloud condensation nuclei, and they are known to interact with developing tropical storms over the Atlantic downwind of the Sahara. Once present within liquid droplets, they have the potential to act as freezing ice nuclei and further affect the microphysics, dynamics, and evolution of tropical storms. However, few measurements of mineral dust particles in tropical convective clouds exist. This study indicates that about one-third of droplets sampled in small convective clouds in the tropical eastern Atlantic contained dust particles, and dust was the dominant residual particle type sampled in ice crystals from anvil outflow. However, estimated number and mass concentrations of dust in anvil ice were small compared to the amount of dust available within the Saharan air layer itself.

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.


Author(s):  
Marion Greilinger ◽  
Anne Kasper-Giebl

Mineral dust is one of the main natural sources of atmospheric particulate matter, with the Sahara being one of the most important source regions for the occurrence and deposition of mineral dust in Europe. The occurrence of dust events in the European Alps is documented via measurements of airborne dust and its deposits onto the glaciers. Dust events occur mainly in spring, summer, and early autumn. Dust layers are investigated in ice cores spanning the last millennium as well as in annual snow packs. They strongly affect the overall flux of dust-related compounds (e.g., calcium and magnesium), provide an alkaline input to wet deposition chemistry, and change the microbial abundance and diversity of the snow pack. Still airborne mineral dust particles can act as ice nuclei and cloud condensation nuclei, influencing the formation of cloud droplets and hence cloud formation and precipitation. Dust deposits on the snow lead to a darkening of the surface, referred to as “surface albedo reduction,” which influences the timing of the snowmelt and reduces the annual mass balance of glaciers, showing a direct link to glacier retreat as observed presently in a warming climate.


2011 ◽  
Vol 11 (12) ◽  
pp. 32363-32390 ◽  
Author(s):  
L. Smoydzin ◽  
A. Teller ◽  
H. Tost ◽  
M. Fnais ◽  
J. Lelieveld

Abstract. We present a numerical modelling study investigating the impact of mineral dust on cloud formation over the Eastern Mediterranean for two case studies: (i) 25 September 2008 and (ii) 28/29 January 2003. On both days dust plumes crossed the Mediterranean and interacted with clouds forming along frontal systems. For our investigation we used the fully online coupled model WRF-chem. The results show that increased aerosol concentrations due to the presence of mineral dust can enhance the formation of ice crystals. This leads to slight shifts of the spatial and temporal precipitation patterns compared to scenarios where dust was not considered to act as ice nuclei. However, the total amount of precipitation did not change significantly. The only exception occurred when dust entered into an area of orographic ascent, causing glaciation of the clouds, leading to a local enhancement of rainfall. The impact of dust particles acting as giant cloud condensation nuclei on precipitation formation was found to be small. Based on our simulations the contribution of dust to the CCN population is potentially significant only for warm phase clouds. Nevertheless, the dust-induced differences in the microphysical structure of the clouds can contribute to a significant radiative forcing.


2011 ◽  
Vol 11 (3) ◽  
pp. 7235-7289 ◽  
Author(s):  
P. Reitz ◽  
C. Spindler ◽  
T. F. Mentel ◽  
L. Poulain ◽  
H. Wex ◽  
...  

Abstract. The ability of coated mineral dust particles to act as cloud condensation nuclei (CCN) and ice nuclei (IN) was investigated at LACIS (Leipzig Aerosol Cloud Interaction Simulator) during the FROST1- and FROST2-campaigns (Freezing of dust). Sulphuric acid was condensed on the particles which afterwards were optionally humidified, treated with ammonia vapour and/or heat. By means of aerosol mass spectrometry we found evidence that processing of mineral dust particles with sulphuric acid leads to surface modifications of the particles. These surface modifications are responsible for the observed reduction of the IN activation of the particles. The observed particle mass spectra suggest that different treatments lead to different chemical reactions on the particle surface. Possible chemical reaction pathways and products are suggested and the implications on IN and CCN efficiency of the treated dust particles are discussed.


2005 ◽  
Vol 5 (4) ◽  
pp. 7211-7245 ◽  
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.


2012 ◽  
Vol 12 (23) ◽  
pp. 11383-11393 ◽  
Author(s):  
L. Smoydzin ◽  
A. Teller ◽  
H. Tost ◽  
M. Fnais ◽  
J. Lelieveld

Abstract. We present a numerical modelling study investigating the impact of mineral dust on cloud formation over the Eastern Mediterranean for two case studies: (i) 25 September 2008 and (ii) 28/29 January 2003. In both cases dust plumes crossed the Mediterranean and interacted with clouds forming along frontal systems. For our investigation we used the fully online coupled model WRF-chem. The results show that increased aerosol concentrations due to the presence of mineral dust can enhance the formation of ice crystals. This leads to slight shifts of the spatial and temporal precipitation patterns compared to scenarios where dust was not considered to act as ice nuclei. However, the total amount of precipitation did not change significantly. The only exception occurred when dust entered into an area of orographic ascent, causing glaciation of the clouds, leading to a local enhancement of rainfall. The impact of dust particles acting as giant cloud condensation nuclei on precipitation formation was found to be small. Based on our simulations the contribution of dust to the CCN population is potentially significant only for warm phase clouds. Nevertheless, the dust-induced differences in the microphysical structure of the clouds can contribute to a significant radiative forcing, which is important from a climate perspective.


2017 ◽  
Author(s):  
Zechen Yu ◽  
Myoseon Jang ◽  
Jiyeon Park

Abstract. The photocatalytic ability of airborne mineral dust particles is known to heterogeneously promote SO2 oxidation, but prediction of this phenomenon is not fully taken into account by current models. In this study, the Atmospheric Mineral Aerosol Reaction (AMAR) model was developed to capture the influence of air-suspended mineral dust particles on sulfate formation in various environments. In the model, SO2 oxidation proceeds in three phases including the gas phase, the inorganic-salted aqueous phase (non-dust phase), and the dust phase. Dust chemistry is described as the adsorption-desorption kinetics (gas-particle partitioning) of SO2 and NOx. The reaction of adsorbed SO2 on dust particles occurs via two major paths: autoxidation of SO2 in open air and photocatalytic mechanisms under UV light. The kinetic mechanism of autoxidation was first leveraged using controlled indoor chamber data in the presence of Arizona Test Dust (ATD) particles without UV light, and then extended to photochemistry. With UV light, SO2 photooxidation was promoted by surface oxidants (OH radicals) that are generated via the photocatalysis of semiconducting metal oxides (electron–hole theory) of ATD particles. This photocatalytic rate constant was derived from the integration of the combinational product of the dust absorbance spectrum and wave-dependent actinic flux for the full range of wavelengths of the light source. The predicted concentrations of sulfate and nitrate using the AMAR model agreed well with outdoor chamber data that were produced under natural sunlight. For seven consecutive hours of photooxidation of SO2 in an outdoor chamber, dust chemistry at the low NOx level was attributed to 70 % of total sulfate (60 ppb SO2, 290 μg m−3 ATD, and NOx less than 5 ppb). At high NOx (> 50 ppb of NOx with low hydrocarbons), sulfate formation was also greatly promoted by dust chemistry, but it was significantly suppressed by the competition between NO2 and SO2 that both consume the dust-surface oxidants (OH radicals or ozone). The AMAR model, derived in this study with ATD particles, will provide a platform for predicting sulfate formation in the presence of authentic dust particles (e.g. Gobi and Saharan dust).


2008 ◽  
Vol 8 (3) ◽  
pp. 11967-11996 ◽  
Author(s):  
C. Mitsakou ◽  
G. Kallos ◽  
N. Papantoniou ◽  
C. Spyrou ◽  
S. Solomos ◽  
...  

Abstract. The desert of Sahara is one of the major sources of mineral dust on Earth, producing around 2×108 tons/yr. Under certain weather conditions, dust particles from Saharan desert get transported over the Mediterranean Sea and most of Europe. The limiting values set by the directive EC/30/1999 of European Union can easily be exceeded by the transport of desert dust particles in all south European areas and especially urban. In this study, the effects of dust transport on air quality in several Greek urban areas are quantified. PM10 concentration values from stationary monitoring stations are compared to dust concentrations for the 4-year period 2003–2006. The dust concentration values in the Greek areas were estimated by the SKIRON modelling system coupled with embedded algorithms describing the dust cycle. The mean annual dust contribution to daily-averaged PM10 concentration values was found to be around or even greater than 10% in the urban areas throughout the years examined. Natural dust transport may contribute by much more than 20% to the annual number of exceedances – PM10 values greater than EU limits – depending on the specific monitoring location. In a second stage of the study, the inhaled lung dose received by the residents in various Greek locations is calculated. The particle deposition efficiency of mineral dust at the different parts of the human respiratory tract is determined by applying a lung dosimetry numerical model, which incorporates inhalation dynamics and aerosol physical processes. The inhalation dose from mineral dust particles was greater in the upper respiratory system (extrathoracic region) and less significant in the lungs, especially in the sensitive alveolar region. However, in cases of dust episodes, the amounts of mineral dust deposited along the human lung are comparable to those received during exposure in heavily polluted urban or smoking areas.


2021 ◽  
Author(s):  
Manuel Gutleben ◽  
Silke Groß ◽  
Martin Wirth

<p>Aeolian Saharan mineral dust particles can be transported over long distances. Great amounts of Saharan mineral dust particles are transported westwards over the Atlantic Ocean towards the Caribbean islands especially during the boreal summer months. During the transport they can either have a direct environmental effect by absorbing, emitting and scattering radiation or an indirect effect by changing cloud micro-physical properties and by modifying cloud lifetime or formation.</p><p>Our recent studies indicate that elevated transported Saharan dust layers, so-called Saharan Air Layers (SALs), come along with enhanced concentrations of water vapor compared to the surrounding atmosphere. Radiative transfer simulations reveal that not the dust particles inside the SALs but the enhanced concentrations of water vapor play the dominant role for atmospheric heating in dust-laden subtropical regions. In this way water vapor has the potential to impact both atmospheric stability and turbulent properties not only inside the SALs but also at lower atmospheric levels.  To study the effects of water vapor on atmospheric turbulence and stability in SAL-regions, we performed wavelet analyses as well as calculations of power spectra on the basis of airborne lidar backscatter and water vapor measurements by the DLR lidar system WALES during the NARVAL-II research campaign. For an in-depth investigation of SAL-properties, several research flights during NARVAL-II were designed to lead over dust-laden regions upstream the Caribbean island of Barbados. Our analysis shows that water vapor heating does not only have an effect on the stability and turbulence of SALs by maintaining their confining inversions and promoting vertical mixing in their interior, but also hinders the development of shallow marine convection below.</p><p>In our presentation we will give an overview of the performed measurements and radiative transfer simulations as well as of the conducted stability and turbulence analyses by means of calculated power spectra and wavelet analyses.</p>


2015 ◽  
Vol 15 (6) ◽  
pp. 3497-3516 ◽  
Author(s):  
N. Bègue ◽  
P. Tulet ◽  
J. Pelon ◽  
B. Aouizerats ◽  
A. Berger ◽  
...  

Abstract. Atmospheric processing and CCN formation of Saharan dust is illustrated through the analysis of a case of dust transport over northern Europe. This spread of dust is investigated by combining satellite, airborne and ground-based observations and the non-hydrostatic meso-scale model Meso-NH. The altitude of the dust plume during its transport to northwestern Europe was assessed using the CALIPSO observations and our model results. The major dust plume was transported toward Mediterranean and European regions between 2 and 5 km above sea level (a.s.l.). This is confirmed by an average particle depolarization ratio equal to 30%. Due to transport, this layer split into two layers over northern Europe, and we analyzed in this paper possible mixing of the European pollution aerosol with dust particles in the lower layer. The simulations have shown that the lower dust layer has interacted with the anthropogenic aerosol mainly over Belgium and the Netherlands. The analyses of numerical simulation results show that mineral dust particles accumulated soluble material through internal mixing over the Netherlands. The value of the CCN0.2 / CN ratio obtained over the Netherlands (~ 70%) is much greater than those observed over the Saharan region. In addition over the Netherlands, the CCN measurement reached 14 000 particles cm−3 at 0.63% supersaturation level on 30 May. Our model results reveal that more than 70% of the CCN concentration observed on 30 May can be explained by the presence of Saharan aged dust. The study reveals that heterogeneous reactions with inorganic salts converted this Saharan mineral dust into compounds that were sufficiently soluble to impact hygroscopic growth and cloud droplet activation over the Netherlands.


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