L. Schütz

Size distribution, mass concentration, chemical and mineralogical composition and derived optical parameters of the boundary layer aerosol at Tinfou, Morocco, during SAMUM 2006

During the SAMUM 2006 field campaign in southern Morocco, physical and chemical properties of desert aerosols were measured. Mass concentrations ranging from 30μgm−3 for PM2.5 under desert background conditions up to 300 000μgm−3 for total suspended particles (TSP) during moderate dust storms were measured. TSP dust concentrations are correlated with the local wind speed, whereasPM10 andPM2.5 concentrations are determined by advection from distant sources. Size distributions were measured for particles with diameter between 20 nm and 500μm (parametrizations are given). Two major regimes of the size spectrum can be distinguished. For particles smaller than 500 nm diameter, the distributions show maxima around 80 nm, widely unaffected of varying meteorological and dust emission conditions. For particles larger than 500 nm, the range of variation may be up to one order of magnitude and up to three orders of magnitude for particles larger than 10μm. The mineralogical composition of aerosol bulk samples was measured by X-ray powder diffraction. Major constituents of the aerosol are quartz, potassium feldspar, plagioclase, calcite, hematite and the clay minerals illite, kaolinite and chlorite. A small temporal variability of the bulk mineralogical composition was encountered. The chemical composition of approximately 74 000 particles was determined by electron microscopic single particle analysis. Three size regimes are identified: for smaller than 500 nm in diameter, the aerosol consists of sulphates and mineral dust. For larger than 500 nm up to 50μm, mineral dust dominates, consisting mainly of silicates, and—to a lesser extent—carbonates and quartz. For diameters larger than 50μm, approximately half of the particles consist of quartz. Time series of the elemental composition show a moderate temporal variability of the major compounds. Calcium-dominated particles are enhanced during advection from a prominent dust source in Northern Africa (Chott El Djerid and surroundings). The particle aspect ratio was measured for all analysed particles. Its size dependence reflects that of the chemical composition. For larger than 500 nm particle diameter, a median aspect ratio of 1.6 is measured. Towards smaller particles, it decreases to about 1.3 (parametrizations are given). From the chemical/mineralogical composition, the aerosol complex refractive index was determined for several wavelengths from ultraviolet to near-infrared. Both real and imaginary parts show lower values for particles smaller than 500 nm in diameter (1.55–2.8 × 10−3i at 530 nm) and slightly higher values for larger particles (1.57–3.7 × 10−3i at 530 nm).

Trace-element concentrations in erodible soils

Abstract Concentrations of 40 elements in 11 desert soils from Africa and North America have been determined as a function of particle size by neutron activation. Concentrations generally increase with decreasing particle size down to radius 10–20 μm, below which they remain nearly constant. This increase is greatest in highly weathered and wind-eroded soils and is negligible in cultivated soils. In the plateau region below 10–20 μm, most elements were within a factor of 2–3 of crustal rock proportions, suggesting that bulk crustal rock is an acceptable reference material for calculating aerosol-crust enrichment factors. The coincidence of the plateau region with the aerosol size range implies that the composition of mineral aerosol should not change markedly during long-range transport; this is borne out by observation. Elements associated with highly resistive minerals such as zircon and rutile can sometimes become unusually enriched in the radius range 10–30 μm.

Mineral aerosols and source identification

Abstract Saharan aerosol and fractionated soil samples have been analysed with X-ray diffraction in order to compare the aerosol mineral composition with its source material. The soil samples used for this study contained only particles with radii r ⩽ 5 μ m generated by a dry fractionation procedure. This soil size fraction can be expected as most relevant for atmospheric processes such as long-range transport, radiation balance, formation and composition of precipitation. The mineral constituents of both types of samples turned out to be rather similar in composition. Even the aerosol samples from the interior of the desert did not show any significant differences which can be attributed to different or typical source regions. The homogeneity of the aerosol composition is obviously due to the fact that the aerosol over the desert itself is already well mixed as a product of continuous deposition and uptake of material from the ground. The composition of the individual soil samples reflects the major petrography. High contents of calcite and palygorskite in samples of the northern desert are the only significant deviations from the average composition. Therefore, calcite and polygorskite can be considered as tracers for atmospheric mineral dust derived from the northern Sahara.

Number, Mass and Volume Distributions of Mineral Aerosol and Soils of the Sahara

Abstract A direct method will be described to determine the complete mineral size distribution in aerosol (xylene-insoluble component) and soils (water-insoluble component) covering a size range from 0.01 up to 100 μm and 1000 μm radius, respectively, by using a combination of a scanning electron microscope, optical microscope and sieving. Aerosol and soil samples from the Sahara have been investigated. All mineral aerosol size distributions indicate a maximum between 0.06 and 0.08 μm radius and mineral particles have been found in the Aitken size range down to 0.02 μm radius. The concentration decrease toward larger particles is not uniform and shows considerable variations below 0.5 μm and above 5 μm radius. Volume distributions show a fairly stable mode around 3 μm and a highly variable mode around 30 μm radius. Particles below 5 μm radius can be considered as a well mixed mineral background aerosol, traveling long distances, whereas larger particles seem to be of local origin, activated under strong w...

Airborne measurements of dust layer properties, particle size distribution and mixing state of Saharan dust during SAMUM 2006

The Saharan Mineral Dust Experiment (SAMUM) was conducted in May/June 2006 in southern Morocco. As part of SAMUM, airborne in situ measurements of the particle size distribution in the diameter range 4 nm < Dp < 100 μm were conducted. The aerosol mixing state was determined below Dp < 2.5 μm. Furthermore, the vertical structure of the dust layers was investigated with a nadir-looking high spectral resolution lidar (HSRL). The desert dust aerosol exhibited two size regimes of different mixing states: below 0.5 μm, the particles had a non-volatile core and a volatile coating; larger particles above 0.5 μm consisted of non-volatile components and contained light absorbing material. In all cases, particles larger than 10 μm were present, and in 80% of the measurements no particles larger than 40 μm were present. The abundance of large particles showed almost no height dependence. The effective diameter Deff in the dust plumes investigated showed two main ranges: the first range of Deff peaked around 5 μm and the second range of Deff around 8 μm. The two ranges of Deff suggest that it may be inadequate to use one average effective diameter or one parametrization for a typical dust size distribution.

Saharan dust absorption and refractive index from aircraft-based observations during SAMUM 2006

During the Saharan Mineral Dust Experiment (SAMUM) conducted in summer 2006 in southeast Morocco, the complex refractive index of desert dust was determined from airborne measurements of particle size distributions and aerosol absorption coefficients at three different wavelengths in the blue (467 nm), green (530 nm) and red (660 nm) spectral regions. The vertical structure of the dust layers was analysed by an airborne high spectral resolution lidar (HSRL). The origin of the investigated dust layers was estimated from trajectory analyses, combined with Meteosat 2nd Generation (MSG) scenes and wind field data analyses. The real part n of the dust refractive index was found almost constant with values between 1.55 and 1.56, independent of the wavelength. The values of the imaginary part k varied between the blue and red spectral regions by a factor of three to ten depending on the dust source region. Absolute values of k ranged from 3.1 × 10−3 to 5.2 × 10−3 at 450 nm and from 0.3 × 10−3 to 2.5 × 10−3 at 700 nm. Groupings of k values could be attributed to different source regions.

Dust mobilization and transport in the northern Sahara during SAMUM 2006 – a meteorological overview

The SAMUM field campaign in southern Morocco in May/June 2006 provides valuable data to study the emission, and the horizontal and vertical transports of mineral dust in the Northern Sahara. Radiosonde and lidar observations show differential advection of air masses with different characteristics during stable nighttime conditions and up to 5-km deep vertical mixing in the strongly convective boundary layer during the day. Lagrangian and synoptic analyses of selected dust periods point to a topographic channel from western Tunisia to central Algeria as a dust source region. Significant emission events are related to cold surges from the Mediterranean in association with eastward passing upper-level waves and lee cyclogeneses south of the Atlas Mountains. Other relevant events are local emissions under a distinct cut-off low over northwestern Africa and gust fronts associated with dry thunderstorms over the Malian and Algerian Sahara. The latter are badly represented in analyses from the European Centre for Medium–Range Weather Forecasts and in a regional dust model, most likely due to problems with moist convective dynamics and a lack of observations in this region. This aspect needs further study. The meteorological source identification is consistent with estimates of optical and mineralogical properties of dust samples.

Electron microscopy of particles collected at Praia, Cape Verde, during the Saharan Mineral Dust Experiment: particle chemistry, shape, mixing state and complex refractive index

A large field experiment of the Saharan Mineral Dust Experiment (SAMUM) was performed in Praia, Cape Verde, in January and February 2008. The aerosol at Praia is a superposition of mineral dust, sea-salt, sulphates and soot. Particles smaller than 500 nm are mainly mineral dust, mineral dust–sulphate mixtures, sulphates and soot–sulphate mixtures. Particles larger then 2.5μm consist of mineral dust, sea-salt and few mineral dust–sulphate mixtures. A transition range exists in between. The major internal mixtures are mineral dust–sulphate and soot–sulphate. Mineral dust–sea-salt mixtures occur occasionally, mineral dust–soot mixtures were not observed. The aspect ratio was 1.3–1.4 for dry particles smaller than 500 nm and 1.6–1.7 for larger ones. Parameterizations are given for dry and humid state. Although the real part of the refractive index showed low variation (1.55–1.58 at 532 nm), a multi-modal imaginary part was detected as function of particle size, reflecting the complex composition. Soot mainly influences the absorption for wavelengths longer than the haematite absorption edge, whereas for shorter wavelengths dust is dominating. The refractive index of the aerosol depends on the source region of the mineral dust and on the presence/absence of a marine component.

Particle Number and Mass Distributions above 10−4 cm Radius in Sand and Aerosol of the Sahara Desert

Abstract Measurements of the particle size distribution in surface air and bulk soil (soil surface and 10 cm depth) were performed in the Sahara desert. This desert is a very important source for mineral dust transported over the Atlantic Ocean. Measurement restrictions limited the size range under investigation to 10−4 to 10−1 cm radius. In that range the size distributions in aerosol (toluene-insoluble component) and soil material (water-insoluble component) are similar in shape, except for a secondary maximum in soil particle size distributions. The results indicate that the aerosol and the soil size distributions are influenced by the soil and wind conditions over large areas. Differences between the soil surface and at depths of 10 cm were not observed within the precision of the measurements. Changes in the shape of the size distribution in the soil or surface air during and after a heavy sandstorm were not observed either—an indication that the loss of sand during a sandstorm is small compared to t...

State of Mixing, Shape Factor, Number Size Distribution, and Hygroscopic Growth of the Saharan Anthropogenic and Mineral Dust Aerosol at Tinfou, Morocco

The Saharan Mineral Dust Experiment (SAMUM) was conducted in May and June 2006 in Tinfou, Morocco. A H-TDMA system and a H-DMA-APS system were used to obtain hygroscopic properties of mineral dust particles at 85% RH. Dynamic shape factors of 1.11, 1.19 and 1.25 were determined for the volume equivalent diameters 720, 840 and 960 nm, respectively. During a dust event, the hydrophobic number fraction of 250 and 350 nm particles increased significantly from 30 and 65% to 53 and 75%, respectively, indicating that mineral dust particles can be as small as 200 nm in diameter. Lognormal functions for mineral dust number size distributions were obtained from total particle number size distributions and fractions of hydrophobic particles. The geometric mean diameter for Saharan dust particles was 715 nm during the dust event and 570 nm for the Saharan background aerosol. Measurements of hygroscopic growth showed that the Saharan aerosol consists of an anthropogenic fraction (predominantly non natural sulphate and carbonaceous particles) and of mineral dust particles. Hygroscopic growth and hysteresis curve measurements of the ‘more’ hygroscopic particle fraction indicated ammonium sulphate as a main component of the anthropogenic aerosol. Particles larger than 720 nm in diameter were completely hydrophobic meaning that mineral dust particles are not hygroscopic.