Evaluation of the method of collecting suspended sediment from large rivers by discharge-weighted pumping and separation by continuous-flow centrifugation

A method for collecting suspended sediment samples has been developed that pumps a discharge-weighted volume of water from fixed depths at four to 40 locations across a river and separates the suspended sediment in the sample using a continuous-flow centrifuge. The efficacy of the method is evaluated by comparing the particle size distributions of sediment collected by the discharge-weighted pumping method with the particle size distributions of sediment collected by depth integration and separated by gravitational settling. The pumping method was found to undersample the suspended sand sized particles (> 63 μm) but to collect a representative sample of the suspended silt and clay sized particles (< 63 μm). The centrifuge separated the silt and clay sized particles (< 63 μm) into three fractions. Based on the average results of processing 17 samples from the Mississippi River and several of its large tributaries in 1990, about 10% of the silt and clay sized material was trapped in a centrifuge bowl-bottom sealing unit containing the nozzle and consisted of mostly medium and coarse silt from 16 to 63 μm. About 74% was retained on a Teflon liner in the centrifuge bowl and consisted of sizes from 0–1 to 63 μm. About 9% was discharged from the centrifuge in the effluent and was finer than 0–1 μm. About 7% was lost during the processes of removing the wet sediment fractions from the centrifuge, drying and weighing. The success of the discharge-weighted pumping method depends on how homogeneously the silt and clay sized particles (< 63 μm) are distributed in the vertical direction in the river. The degree of homogeneity depends on the composition and degree of aggregation of the suspended sediment particles.     

MELIMEX,an experimental heavy metal pollution study: Particle size distributions in limno-corrals

The particle size distributions in three limno-corrals, located in Baldeggersee, Switzerland, have been determined by means of a Zeiss Micro-Videomat image analyzer as a function of depth and time. The distributions were measured biweekly over a period of 1 year at depths of 0 m, 2.5 m, 5 m, 7.5 m and 10 m (=above bottom). Two of the limno-corrals were charged with heavy metals, whereas the third was uncharged and served as a reference. The shape of the distributions as well as the particle concentrations in the uncharged container did not differ from the ones in the charged limno-corrals. The distributions were found to be self-preserving and independent on heavy metal load, time, depth and particle concentrations. As an average, the dependence of the distributions on the particle diameter was found to be ?1.5 to ?2.5.     

Effects of continuous flow centrifugation on measurements of trace elements in river water: intrinsic contamination and particle fragmentation

Continuous flow centrifugation (CFC) is a well‐established technique used in natural surface water studies to collect large amounts of suspended solids, thus allowing a broad spectrum of measurements. However, a potential contamination or changes in the particle size distribution during the centrifugation may restrain the use of CFC effluents for element analysis in the colloidal and dissolved fractions. In this paper we evaluate the possibility of using the effluent of a Westfalia centrifuge (type KA2‐06‐075, 9700 rpm) for such analysis. This evaluation is based on two laboratory experiments with deionized and tap water and two field experiments in rivers. Elemental concentration changes across the CFC were assessed from the CFC influent and effluent after a filtration at 0·45 µm. Significant increases were found, mainly in the field experiments at a high suspended solids level and a slightly acid pH. A hypothesis was made on the origin of these increases as a superposition of a centrifuge intrinsic contamination and a particle fragmentation effect. A numerical model based on elemental concentration measurements (inductively coupled plasma mass spectrometry) gave a particle fragmentation level of 0·55% (mass percentage of particles broken up into smaller fragments during centrifugation). In another experiment, a direct particle counting (single particle counter) shows an excess of particles smaller than 500 nm in the CFC effluent, corresponding to a fragmentation level of 0·11%. In consequence, the use of CFC effluent for element analysis is possible in low‐turbidity river or lake waters, but should be carefully considered in waters with high suspended matter contents. Copyright © 2006 John Wiley & Sons, Ltd.     

Characterization of colloidal and particulate matter transported by the magela creek system,Northern Australia

The composition and amount of colloidal and suspended participate matter transported during a small flood event in Magela Creek in tropical northern Australia was investigated. The flood studied constituted approximately 3 % of the total annual flow, most (90%) of which occurred between mid-January and mid-February of the study year. Three fractions were separated from water samples using a sequential method involving a continuous flow centrifuge to separate suspended particulate matter (SPM; nominally > 1 μm) followed by hollow fibre filtration, first using a 0.1 μm filter to separate course colloidal matter (CCM; nominal size 1–0.1 μm) and then a 0–015 μm filter to separate fine colloidal matter (FCM; nominal size 0.1–0.015 μm). The SPM was predominantly inorganic (organic matter 21 %), whereas the colloidal fractions were dominantly organic matter (CCM 60%; FCM 83%). Analysis of individual particles using electron microprobe and automated image analysis indicated that the mineral fractions in both the SPM and CCM were dominated by iron-enriched aluminosilicates (including kaolinite) (72–82%) and quartz (9–10%), indicative of a highly weathered and extensively laterized catchment. Surprisingly there was very little difference in the composition of the SPM or CCM fractions during the flood event studied, which may indicate either that sediment availability was restricted following the major run-off events in January and February, or that all the sediment sources within the catchment are geochemically similar. Approximately the same amounts of particulate (20 tonne), colloidal (21 tonne) and dissolved material (17 tonne) were transported during the 25 hour period of the main flood peak; over 90% of the colloidal matter was 0.1–1.0 μm in size. These data suggest that previous estimates of the amounts of particulate (and colloidal) matter transported by Magela Creek, which were based on suspended solids measurements, may have underestimated the particulate matter load by as much as 50%. It is possible that the relatively high proportion of colloidal matter is unique to Magela Creek because coagulation and aggregation of colloidal matter to particulate matter is slow due to the very low concentations of calcium and magnesium in these waters. However, if the result is more widespread, there are important implications for the global estimates of fluvially transported particulate and dissolved materials as many of the previous studies may have underestimated the particulate load and overestimated the dissolved load.     

Characterization of particle size and settling velocity of cohesive sediments affected by a neutral exopolymer

In natural waters,exopolymers or extracellular polymeric substances(EPS) exuded by microorganisms interact with clay particles,resulting in the flocculation of clays and hence alteration to the properties of suspended cohesive sediments.To investigate and further understand how neutral EPS affect cohesive sediment transport and the final sediment yield,an experimental study was conducted on laboratory-prepared clay and guar gum(used as an analog for neutral EPS) suspensions to characterize EPS-induced flocculation and the settling velocity of resultant floes.Four different clays consisting of kaolinite,illite,Ca-montmorillonite,and Na-montmorillonite were studied to examine the influence of different layer charges on clay flocculation induced by neutral EPS.Floc size was determined by a laser particle size analyzer,and settling velocity estimated by analyzing the time-series floc settling images captured by an optical microscope.Results indicate that neutral EPS promote clay-EPS flocculation for all four clays with the particle/floc size significantly increased from～0.1-60μm to as large as～600μm.Clays’ layer charge has a profound influence on the clay-EPS flocculation.With the same floc size,the settling velocity of clay-EPS flocs is typically smaller than that of pure clay flocs,which is attributed to the reduced density of flocs caused by the EPS. However,for flocs of the same composition(e.g.pure clay or hybrid clay-EPS mixture),the settling velocity increases with size.The fractal dimension of these clay-EPS flocs estimated from settling velocity ranges from 1.39 to 1.47,which are smaller than that of pure clay flocs,indicating that these flocs are less compacted than the pure clay flocs.     

Rayleigh scattering by aqueous colloidal silica as a cause for the blue color of hydrothermal water

Thermal waters in hydrothermal ponds, bathing pools and the brines of geothermal electric power plants commonly have a characteristic blue color. Although many researchers have assumed that the blue color is due to a colloidal suspension and/or absorption by dissolved ferrous iron or by water itself, there has been no specific effort to identify the physical nature of this phenomenon. We have tested, in synthetic and natural solutions, whether aqueous colloidal silica is responsible for the blue color. Aqueous colloidal silica is formed by silica polymerization in thermal waters of the neutral-chloride type which contain initially monomeric silica in concentrations up to three times above the solubilities of amorphous silica. The hue of the blue thermal waters in the pools tested agrees with that of a synthesized colloidal silica solution. Grain-size analyses of aqueous colloidal silica in the blue-colored thermal waters demonstrate that the color is caused by Rayleigh scattering from aqueous colloidal silica particles with diameters (0.1–0.45 μm) smaller than the wavelengths of visible radiation.     

Features of interaction between lake water and springs,and evaluation of hydrochemical composition of water in Ifni Lake (High Atlas Mountains,Morocco, north of Africa)

The National Park of Toubkal is located in the High Moroccan Atlas Mountains, one of the regions sheltering the highest summits of North Africa (Mount Toubkal with an elevation of 4167 m). The park is characterized by very important water resources, including Ifni Lake, which is the highest natural lake in Morocco (with an elevation of 2320 m). This lake is located on the southern side of Mt. Toubkal. This area has never been the object of an environmental or hydrological study. The objective of the current study was the characterization of Ifni Lake and the spring waters located in this area, as the basis of a framework to protect natural resources in northern Africa. The hydrochemical composition of water determines its origin and relationship with its catchment. Hydrochemical studies were carried out to assess the ions water composition, and processes governing the hydrochemistry of Ifni Lake water and the springs in the study area. A total of 20 water samples were collected in 2013 and analyzed for various parameters such as pH, electrical conductivity, and major ions. The physico-chemical analysis of the Ifni Lake water showed that this is the least mineralized water studied in this region, having a bicarbonate, calcium, and magnesium as dominate ions. Also there is a relationship between the hydrochemical composition of Ifni Lake and spring waters.     

Discrete suspended particles of barite and the barium cycle in the open ocean

Barite particles are a universal component of suspended matter in the Atlantic and Pacific Oceans. This is demonstrated by scanning electron microscope and electron microprobe analyses of samples collected during the GEOSECS program. These discrete particles, about 1 μm in diameter, account for by far the greatest part of the total particulate barium of most of the filters collected at different depths. Total particulate barium (mean value: 20 ng/kg seawater) was measured on the same filters by instrumental neutron activation analysis.Several observations indicate that biochemical, rather than purely chemical, processes are involved in the formation of the BaSO₄ mineral in the water column. Sr/Ba molar ratios among the individual barite grains, particularly from surface waters are extremely variable, which would not be anticipated for purely chemical interactions. Barite crystals occurring within fecal debris have been observed throughout the water column. Within such debris decomposition of the abundant organic matter may provide the micro-environment predicted as necessary for the precipitation of BaSO₄. Finally, a strong correlation between nutrient content and particulate barium is found in the upper 1000 m of the water column, which also suggests a control of barite formation by biota.Some of the barite dissolves at depth in the water column. Dissolution rates were calculable for two GEOSECS stations, from which a dissolved barium flux of 0.4 μg/cm² yr was deduced. This figure is of the same order as the dissolved barium flux calculable from the barium content and known dissolution rates of calcareous and siliceous tests: approximately 0.5 μg/cm² yr. These fluxes represent the largest source of dissolved barium in the water column, the other being river input (0.6 μg/cm² yr). This supports the contention that the barium in the water column is mostly recycled. The residual flux of barite-Ba reaching the sea floor is of about equal importance as the flux of barium associated with fast-settling fecal material. These two sources together are almost sufficient to account for the total sedimentation rate of barium.     

The distribution of particulate matter in the Atlantic Ocean

We have determined the dry weight of suspended particulate matter in seawater in a section through the western Atlantic Ocean from 75°N to 52°S. The concentrations, operationally defined as that weight retained on 0.6-μm and 0.4-μm pore size Nuclepore filters, contained in 1 kg of seawater, range from 5 to 300 μg/kg and show readily explainable regional features. High concentrations are found in surface waters and in association with radpidly moving bottom waters in the Denmark Straits overflow and in Antarctic bottom waters to 15°S. Low concentrations, <12 μg/kg, characterize the mid-water regions of the sub-tropical gyres. High concentrations are seen in sinking Labrador Sea water and in a plume extending at least a kilometer off the bottom at 35°N–40°N where the cruise track intersects the North Atlantic gyre. It is doubtful whether this important phenomenon could be observed by any means other than through particulate observations, either optical or gravimetric, and this provides a unique insight into the scale of vertical turbulent processes.     

The Concentrations of Cadmium,Lead and Copper in Filtrated Baltic Sea Water Samples Collected at Two Seasons in 1969

Two research cruises on the Baltic Sea, in July and November of 1979, were made for investigating the Baltic Sea water for its contents of dissolved cadmium, lead and copper. Atomic absorption spectrophotometry and voltammetry were used as methods of investigation, the latter method having supplied slightly lower results. In the water layer of 0 … 50 m the cadmium concentrations were 0.03 … 0.05 μg/l and the lead concentrations were 0.1 … 0.2 μg/l, seasonal changes did not have any effect on them. The copper concentrations, on the other hand, were 0.4 … 1.2 μg/l in summer and 0.1 … 0.7 μg/l in autumn. Compared with ocean waters, the lead content is remarkably high. In anoxic deep waters of the Baltic Sea the concentrations of the three metals, especially that of cadmium, are very low (< 0.01 μg/l).     

Removal of Selenium Species from Waters Using Various Surface‐Modified Natural Particles and Waste Materials

Waste red mud and natural pumice/volcanic slag particles were surface modified and their selenium adsorption from waters was investigated. Acid activation/heat treatment of original red mud (ORM) particles significantly increased their micropore and external surface area and cumulative volume of pores. Iron oxide coating of pumice/slags and acid activation of ORM decreased their pH_pzc values and increased surface acidity. Selenite/selenate adsorption on iron oxide surfaces and acid activated red mud (AARM) was very fast with approximately first‐order adsorption kinetics. Iron oxide coating of pumice/slag and acid activation of ORM particles significantly enhanced their selenite and selenate uptakes. Maximum Se adsorption capacities as high as 6.3 (mg Se/g adsorbent) were obtained by AARM. The extent of selenate uptakes by the surface modified particles was generally lower than those of selenite. Due to competition among Se species and other background water matrix for iron oxide adsorption sites, reduced selenite/selenate uptakes were found in natural water compared to single solute tests. Higher Se uptakes by iron oxide surfaces were found at pH 7.5 compared to pH 8.9, due to increased electrostatic repulsion among iron oxides and Se species at higher pH. The most effective adsorbents among the tested 17 different particles for Se uptake were AARM and iron oxide coated pumice. Se concentrations less than drinking water standards (5–10 µg/L) can be achieved by these particles. These low‐cost, natural, or recyclable waste particles appear to be promising adsorbents for Se removal after their surface modification.     

Disequilibria between ~(210)Po and ~(210)Pb in surface waters of the southern South China Sea and their implications

Naturally occurring 210Po (half-life 138.4d) is the granddaughter of 210Pb (half-life 22.3a), both are members of 238U decay series and have been inten-sively utilized to study kinetic aspects of material cy-cling in the ocean[1]. Based on radioactive disequilibria in the 226Ra-210Pb-210Po system, oceanographical processes with different timescales have been widely studied. Rama et al.[2] first detected excess 210Pb rela-tive to its precursor 226Ra in surface waters, and considered this exc…     

Use of a single-bowl continuous-flow centrifuge for dewatering suspended sediments: Effect on sediment physical and chemical characteristics

The use of a single-bowl continuous-flow centrifuge (CFC, Sharples-Pennwalt Model AS-12) for dewatering suspended sediment from large volumes of river water is evaluated. Sediment-recovery efficiency of 86-91 per cent is comparable to that of other types of CFC units. The recovery efficiency is limited by the particle-size distribution of the feed water and by the limiting particle diameter that is retained in the centrifuge bowl. The limiting particle diameter, using the parameters for this study (bowl radius = 10.5cm; bowl length = 71.1 cm; rotational velocity = 16000 r min^?1; flow rate = 2 L min^?1, and an assumed hydrated particle density = 1.7 gm cm^?3), is 370 nm. There seems to be no particle-size fractionation within the centrifuge bowl—the median particle size was the same at the top as at the bottom. Particle electrophoretic mobility plays some role in fractionation of particles within the centrifuge. The mobility ranged from ?1.19 to ?2.01 × 10^?8 m² V^?1 s^?1, which is typical of clays coated with organic matter, the charge of which is partially neutralized by divalent cations and iron. Contamination by trace metals and organics is minimized by coating all surfaces that come in contact with the sample with either FEP or PFA Teflon and using a removable FEP Teflon liner in the centrifuge bowl. Because of the physical and chemical factors affecting particle fractionation within the centrifuge, care must be exercised in interpreting the environmental consequences of particles collected by continuous-flow centrifugation.     

Bakterienvermehrungsmessungen in aufbereiteten Wässern verschiedener Herkunft

Bacterial growth measurements in treated waters from different origins. Measuring growth curves of bacteria in a drinking water gives information on the regrowth potential of the water in the pipe system. The method which was developed by Werner was used for analyzing drinking waters from different origins. As a negative control high purity water and as positive control acetate were used. It is proposed to use acetate-C-equivalents for quantification because the biodegradable part of total dissolved organic carbon (DOC) is mostly below 0,1 mg/1 in treated waters. The analyses of treated surface waters showed results from 40–80 μg/1 acetate-C-equivalents, whereas in treated waters from ground water and bankfiltrates the concentration of easily biodegradable organic carbon was between 10 and 20 μg/1 acetate-C-equivalents. This is in the region of high purity water, where in average 9 μg/1 acetate-C-equivalents are detected, which therefore is the detection limit of the method. These waters normally do not show any regrowth problems.     

Micro- and macro-observations of liquefaction of saturated sand around buried structures in centrifuge shaking table tests

A novel experimental method was designed to study the micro-behavior of saturated sand around a buried structure in centrifuge shaking table tests under strong simulated earthquake loading, in addition to the traditional macro-measurements. One free field test was first carried out as a reference, followed by one test with a deep buried structure and one with a shallowly buried structure. During the tests with the buried structure, high quality pictures of moving sand around the structure were recorded by a newly developed image acquisition system. By analyzing the interesting pictures at reasonable intervals using an image analysis software, the evolutions of microstructural features were obtained such as the orientations of the long axes of particles, the orientations of contact normals between particles and the average contact number of the interesting group of particles. The results showed that the evolutions of the micro-features were consistent with those of the macro-measurements such as excess pore pressures and accelerations, which help illuminate the mechanism of sand liquefaction.     

Identifizierung ausgewählter Pestizide im Wasser mit Hilfe eines screening-Systems auf Grundlage der Dünnschichtchromatographie

After their extraction from water, 16 water pollutants of the families of triazines, urea herbicides, phenoxycarboxylic acids and organochlorine and organophosphorus insecticides are separated and identified by thin-layer chromatography. The method is suitable for routine analyses and was tested on model waters, inclusive of water from the Elbe river. The rate of redetection is up to 80%, the detection limit is at 0.5… 2 μg of the individual pollutants.     

Chlorinated hydrocarbons in lower continental slope fish collected near the Farallon Islands,California

During December, 1985, Dover sole (Microstomus pacificus) were collected at water depths of 500 and 1000 m and sablefish (Anoplopoma fimbria) were collected at a water depth of 1000 m in the vicinity of former low-level radioactive and chemical munition disposal sites located near the Farallon Islands, California. Liver tissues were analysed for chlorinated hydrocarbons by gas chromatography with electron capture detection (GC/ECD). Chlorinated hydrocarbons (DDTs and PCBs) were detected in all fish. Concentrations of total DDTs and PCBs in livers of Dover sole and sablefish were as high as, or higher than, those recently reported for the same species collected in heavily contaminated coastal waters of Southern California. The presence of DDTs (up to 9 μg g⁻¹, wet wt) and PCBs (up to 7 μg g⁻¹, wet wt) in fish livers may indicate extensive contamination of the coastal waters or bottom sediments in the vicinity of the Farallon Islands. Even though the definitive sources of the chlorinated hydrocarbons detected in the Dover sole and sablefish are not known, the relative proximity of the former chemical munition disposal sites indicates that these areas may be a potential source of one or both of these contaminants.     

Occurrence and Distribution of Organic Contaminants in the Aquatic System in Berlin. Part III: Determination of Synthetic Musks in Berlin Surface Water Applying Solid-phase Microextraction (SPME) and Gas Chromatography-Mass Spectrometry (GC-MS)

Polycyclic musks and nitro musks were found as environmental pollutants in screening analyses of 30 representative surface water samples collected from rivers, lakes, and canals in Berlin. These synthetic musks, which are used as fragrances in cosmetics, detergents, and other products, are discharged by the municipal sewage treatment plants into Berlinπs surface waters. In particular, the polycyclic musks 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-(g)-2-benzopyrane (HHCB; Galaxolide®, Abbalide®) and 7-acetyl-1,1,3,4,4,6-hexamethyltetraline (AHTN; Tonalide®, Fixolide®) were found in the receiving surface waters at considerable concentrations up to the μg/L-level. In the Wuhle, a small brook almost totally consisting of sewage effluents, maximum concentrations were 12.5 μg/L for HHCB and 6.8 μg/L for AHTN. Additionally, the polycyclic musk 4-acetyl-1,1-dimethyl-6-tert-butylindane (ADBI; Celestolide®, Crysolide®) and 1-tert-butyl-3,5-dimethyl-2,6-dinitro-4-acetylbenzene (musk ketone) were detected at low concentrations in most of the samples. Two other nitro musks, namely 1,1,3,3,5-pentamethyl-4,6-dinitroindene (musk moskene) and 1-tert-butyl-3,5-dimethyl-2,4,6-trinitrobenzene (musk xylene), were only detected in a single surface water sample. Solid-phase microextraction (SPME) with detection by gas chromatography-mass spectrometry (GC-MS) has proven to be a rapid and reliable tool for the screening of synthetic musks in surface and sewage water samples. Internal calibration with a suitable internal standard enables reproducible quantitation of the analytes down to the low ng/L-level.     

Determination of arsenic(III) for the investigation of the microbial oxidation of arsenic(III) to arsenic(V)

Recent evaluations of acute and chronical toxicity of arsenic resulted in a reduction of the standard value for total arsenic from 40 μg/L to 10 μg/L in drinking water which will be valid in Germany after a transition period as from January 1996. Arsenic is well known as substance of deep groundwaters, mainly of geogenic origin and normally found as As(III) or As(V). As(V) is well removable by flocculation and filtration after adding iron salts. As(III), however, has to be oxidized first to As(V). Therefore, it is important for treatment techniques to be able to distinguish between As(III) and As(V). A modified determination of As(III) using flow injection analysis was installed and optimized in order to investigate whether As(III) may be oxidized to As(V) by bacteria in natural waters. The results showed that at 4°C, no As(III)-oxidation was observed within 14 days. At room temperature, however, in the bacteria-containing samples, an As(III)-oxidation was found starting after 3 to 7 days. After 14 days, no As(III) was left over. In contrast, in the sterile samples, no As(III)-oxidation could be observed within 14 days. These results demonstrated that microbial processes influence the oxidation of As(III) to As(V) in natural waters.