MELIMEX,an experimental heavy metal pollution study: Effects of increased heavy metal load on uptake of glucose by natural planctonic communities

Glucose uptake in lake water samples has been determined with short-time¹⁴C-experiments at different additions of the single heavy metals Cu⁺⁺, Zn⁺⁺, Cd⁺⁺, Pb⁺⁺, Hg⁺⁺ and at different additions of a combination of all metals. The degree of a metal induced inhibition of glucose uptake varied from lake to lake and from season to season, whereby the addition of legally tolerated concentrations of 10 μg Cu/l and 200 μg Zn/l inhibited glucose uptake in most samples significantly, as well as the simultaneous addition of all metals. The legally tolerated limit of 1 μg Hg/l inhibited glucose uptake in Lake Lucerne samples almost completely, showed however no effect in samples of Lake Baldegg. The equimolar toxicity sequence of heavy metals for heterotrophic microorganisms has been determined as: Hg>Cu>Cd>(Zn. Pb). Glucose uptake of plankton sampled from metal polluted limno-corrals was less inhibited than that of the control plankton, when heavy metals were added to the samples singly or in combination. It is assumed that this effect is due to the natural selection of more resistant plankton species.     

Natural shock behavior of almandite in metamorphic rocks from the ries crater,Germany

An extensive study of a big number of gneiss specimens with various shock features from the suevite allowed unravelling of the shock behavior of almandite garnets.Almandites in shocked metamorphic rocks show with increasing dynamic pressures strong irregular fracturing. differently oriented sets of planar fractures or elements, brown turbidity and nucleation of minute crystals of an unknown phase in solid garnets. At higher peak pressures garnet was found to break down to (1) orthopyroxene + spinel + glass, and to (2) spinel + glass due to fast shock-melting.Extensive quantitative electron microprobe studies of almandite garnets and their breakdown products were carried out. The breakdown products within the original grain boundaries of the garnets consist of an alumina-rich orthopyroxene (with up to 10 wt. % Al₂O₃), hercynite to pleonaste spinels and a silica and calcium-rich glass matrix. The chemical zonation of magnesium and manganese of the former garnets is inherited in the composition of the newly formed orthopyroxenes.Petrographic evidence and chemical composition suggest a fast breakdown of the almandite garnets after passing of shock waves at rapidly falling pressures and very high post-shock temperatures within the ejected gneissic rock material.     

The provenance of northern Kalahari Basin sediments and growth history of the southern Congo Craton reconstructed by U–Pb ages of zircons from recent river sands

The southern Congo Craton is widely overlain by Meso- to Cenozoic sediments of the northern Kalahari Basin, which hamper any correlation of basement units. The latter are represented by the Archaean Angola and Kasai Blocks, while the southern cratonic margin is framed by several Meso- to Neoproterozoic orogenic belts. For provenance analysis of the sedimentary cover and reconstruction of the main zircon-forming events, we studied zircons from recent sediments of the largest rivers at the southern margin of the Congo Craton. U–Pb zircon ages suggest a major amount of the sediments to originate from E Lufilian and Kibaran Belts, while input from the S Damara Belt seems to increase to the W. Ages related to the Angola Block were only noticed in the westernmost parts of the working area, which is not in accordance with the SE-trending drainage pattern, proposed to have been onset during the Cretaceous. Thus, it is assumed that the Meso- to Cenozoic sedimentary cover extended further west than today prior to the Mesozoic to Neogene uplift of the Angola Block and that subsequent erosion exhumed the basement stepwise from west to east. A recurrent destabilisation of the southern margin of the Congo Craton at ~2.7, 1.9, 1.0 and 0.6 Ga is supposed to be represented by major peaks in the age distribution pattern of the total amount of concordant zircons. This is in accordance with similar studies in adjacent areas. Additionally, the obtained data fit well to several hypothesised major events during the supercontinent cycle.     

Evaluation of trace element availability from secondary metallurgical slag generated in steelmaking by sequential chemical extraction

During carbon steel manufacture, slag residues are generated to remove material impurities from liquid metal and thus control the quality of carbon steel. As the utilization of secondary metallurgical slags is not as efficient as those of primary slags, a comprehensive characterization of steel ladle slag was performed. Pseudo-total concentrations of a wide range of elements were determined during a 6-week sampling period with relevant physical and chemical properties, sequential extraction of trace elements, and parallel mineralogical characterization of extraction residues from a representative combined sample. According to the results, only Cr and V occurred in elevated concentrations with respective 6-week mean values of 198 and 310 mg kg^?1 (d.w.). The residual standard deviation of the weekly pseudo-total concentration values of the aforementioned elements (24 and 31 %, respectively) indicated that significant variation in the concentration of trace elements can occur due to fluctuation in process conditions and/or slag characteristics. The sequential extraction procedure suggested potential phytoavailability of V (123 mg kg^?1, d.w., amounting to 41 % of the respective pseudo-total concentration) through, e.g., changes in prevailing redox conditions. Although the analytical approach was validated by the analysis of a certified reference material and the calculation of extraction recoveries, the mineralogical characterization of parallel extraction residues indicated non-selectivity of the procedure coupled with potential redistribution phenomena during extraction with hydrogen peroxide and ammonium acetate.     

Platinum-group element distribution in base-metal sulfides of the Merensky Reef from the eastern and western Bushveld Complex, South Africa

Base-metal sulfides in magmatic Ni-Cu-PGE deposits are important carriers of platinum-group elements (PGE). The distribution and concentrations of PGE in pentlandite, pyrrhotite, chalcopyrite, and pyrite were determined in samples from the mineralized portion of four Merensky Reef intersections from the eastern and western Bushveld Complex. Electron microprobe analysis was used for major elements, and in situ laser ablation inductively-coupled plasma mass spectrometry (LA-ICP-MS) for trace elements (PGE, Ag, and Au). Whole rock trace element analyses were performed on representative samples to obtain mineralogical balances. In Merensky Reef samples from the western Bushveld, both Pt and Pd are mainly concentrated in the upper chromitite stringer and its immediate vicinity. Samples from the eastern Bushveld reveal more complex distribution patterns. In situ LA-ICP-MS analyses of PGE in sulfides reveal that pentlandite carries distinctly elevated PGE contents, whereas pyrrhotite and chalcopyrite only contain very low PGE concentrations. Pentlandite is the principal host of Pd and Rh in the ores. Palladium and Rh concentrations in pentlandite reach up to 700 and 130 ppm, respectively, in the samples from the eastern Bushveld, and up to 1,750 ppm Pd and up to 1,000 ppm Rh in samples from the western Bushveld. Only traces of Pt are present in the base-metal sulfides (BMS). Pyrrhotite contains significant though generally low amounts of Ru, Os, and Ir, but hardly any Pd or Rh. Chalcopyrite contains most of the Ag but carries only extremely low PGE concentrations. Mass balance calculations performed on the Merensky Reef samples reveal that in general, pentlandite in the feldspathic pyroxenite and the pegmatoidal feldspathic pyroxenite hosts up to 100 % of the Pd and Rh and smaller amounts (10–40 %) of the Os, Ir, and Ru. Chalcopyrite and pyrrhotite usually contain less than 10 % of the whole rock PGE. The remaining PGE concentrations, and especially most of the Pt (up to 100 %), are present in the form of discrete platinum-group minerals such as cooperite/braggite, sperrylite, moncheite, and isoferroplatinum. Distribution patterns of whole rock Cu, Ni, and S versus whole rock Pd and Pt show commonly distinct offsets. The general sequence of “offset patterns” of PGE and BMS maxima, in the order from bottom to top, is Pd in pentlandite?→?Pd in whole rock?→?(Cu, Ni, and S). The relationship is not that straightforward in general; some of the reef sequences studied only partially show similar trends or are more complex. In general, however, the highest Pd concentrations in pentlandite appear to be related to the earliest, volumetrically rather small sulfide liquids at the base of the Merensky Reef sequence. A possible explanation for the offset patterns may be Rayleigh fractionation.