Evolution of the palaeolake at Ruszkówek (central Poland) during the Eemian Interglacial based on isotope,cladoceran and diatom data

We present isotope, cladoceran and diatom results from investigations of Eemian sediments of the palaeolake at Ruszkówek, central Poland. Our analyses of the 15-m-thick sediments indicate that sandy silts occur on the bottom, followed by calcareous gyttja, interbedded with lake marl. The upper part of the sequence contains peat and peaty sands. Values of δ¹⁸O change from −9.4‰ to −3.3‰ and δ¹³C values oscillate between −3.2‰ and +7.0‰. Nine isotope zones (Is) were defined and characterized using stable isotope analysis of carbonates. Fifteen species of subfossil Cladocera were found and six faunal zones were distinguished (Cladocera zones). One hundred and twenty-three diatom taxa, representing 31 genera were identified, enabling us to discern six Diatom Assemblage Zones. The isotope, cladoceran, and diatom data correlate well with pollen data that define seven phases of evolution of the palaeolake at Ruszkówek. The palaeolake began during the final phase of the Wartanian (Late Saalian Glaciation). During the early Eemian, the palaeolake reached its maximum depth. During the Early Vistulian glaciation, the palaeolake declined. Changes in the cladoceran and diatom communities indicate initial oligotrophic conditions in the lake, then an increase to mesotrophy, and finally eutrophic conditions.     

Spectroscopic studies of synthetic and natural ringwoodite, γ-(Mg,Fe)<Subscript>2</Subscript>SiO<Subscript>4</Subscript>

Synthetic ringwoodite γ-(Mg_1?x Fe _x )₂SiO₄ of 0.4 ≤ x ≤ 1.0 compositions and variously colored micro-grains of natural ringwoodite in shock metamorphism veins of thin sections of two S6-type chondrites were studied by means of microprobe analysis, TEM and optical absorption spectroscopy. Three synthetic samples were studied in addition with Mössbauer spectroscopy. The Mössbauer spectra consist of two doublets caused by ^VIFe²⁺ and ^VIFe³⁺, with IS and QS parameters close to those established elsewhere (e.g., O’Neill et al. in Am Mineral 78:456–460, 1993). The Fe³⁺/Fe_total ratio evaluated by curve resolution of the spectra, ranges from 0.04 to 0.1. Optical absorption spectra of all synthetic samples studied are qualitatively very similar as they are directly related to the iron content. They differ mostly in the intensity of the observed absorption features. The spectra consist of a very strong high-energy absorption edge and a series of absorption bands of different width and intensity. The three strongest and broadest absorptions of them are attributed to splitting of electronic spin-allowed ⁵ T _2g → ⁵ E _g transitions of ^VIFe²⁺ and intervalence charge-transfer (IVCT) transition between ferrous and ferric ions in adjacent octahedral sites of the ringwoodite structure. The spin-allowed bands at ca. 8,000 and 11,500 cm^?1 weakly depend on temperature, whilst the Fe²⁺/Fe³⁺ IVCT band at ~16,400 cm^?1 displays very strong temperature dependence: i.e., with increasing temperature it decreases and practically disappears at about 497 K, a behavior typical for bands of this type. With increasing pressure the absorption edge shifts to lower energies while the spin-allowed bands shift to higher energy and strongly decreases in intensity. The IVCT band also strongly weakens and vanishes at about 9 GPa. We assigned this effect to pressure-induced reduction of Fe³⁺ in ringwoodite. By analogy with synthetic samples three broad bands in spectra of natural (meteoritic) blue ringwoodite are assigned to electronic spin-allowed transitions of ^VIFe²⁺ (the bands at ~8,600 and ~12,700 cm^?1) and Fe²⁺/Fe³⁺ IVCT transition (~18,100 cm^?1), respectively. Spectra of colorless ringwoodite of the same composition consist of a single broad band at ca. 12,000 cm^?1. It is assumed that such ringwoodite grains are inverse (Fe, Mg)₂SiO₄-spinels and that the single band is caused by the split spin-allowed ⁵ E → ⁵ T ₂ transition of ^IVFe²⁺. Ringwoodite of intermediate color variations between dark-blue and colorless are assumed to be partly inversed ringwoodite. No glassy material between the grain boundaries in the natural colored ringwoodite aggregates was found in our samples and disprove the cause of the coloration to be due to light scattering effect (Lingemann and Stöffler in Lunar Planet Sci 29(1308), 1998).     

Geochemistry,mineralogy, and zircon U–Pb–Hf isotopes in peraluminous A-type granite xenoliths in Pliocene–Pleistocene basalts of northern Pannonian Basin (Slovakia)

Anorogenic granite xenoliths occur in alkali basalts coeval with the Pliocene–Pleistocene continental rifting of the Pannonian Basin. Observed granite varieties include peraluminous, calcic to peralkalic, magnesian to ferroan types. Quartz and feldspars are dominant rock-forming minerals, accompanied by minor early ilmenite and late magnetite–ulvöspinel. Zircon and Nb–U–REE minerals (oxycalciopyrochlore, fergusonite, columbite) are locally abundant accessory phases in calc-alkalic types. Absence of OH-bearing Fe, Mg-silicates and presence of single homogeneous feldspars (plagioclase in calcic types, anorthoclase in calc-alkalic types, ferrian Na-sanidine to anorthoclase in alkalic types) indicate water-deficient, hypersolvus crystallization conditions. Variable volumes of interstitial glass, absence of exsolutions, and lacking deuteric hydrothermal alteration and/or metamorphic/metasomatic overprint are diagnostic of rapid quenching from hypersolidus temperatures. U–Pb zircon ages determined in calcic and calc-alkalic granite xenoliths correspond to a time interval between 5.7 and 5.2 Ma. Positive εHf values (14.2 ± 3.9) in zircons from a 5.2-Ma-old calc-alkalic granite xenolith indicate mantle-derived magmas largely unaffected by the assimilation of crustal material. This is in accordance with abundances of diagnostic trace elements (Rb, Y, Nb, Ta), indicating A₁-type, OIB-like source magmas. Increased accumulations of Nb–U–REE minerals in these granites indicate higher degree of the magmatic differentiation reflected in Rb-enrichment, contrasting with Ba-enrichment in barren xenoliths. Incipient charnockitization, i.e. orthopyroxene and ilmenite crystallization from interstitial silicate melt, was observed in many granite xenoliths. Thermodynamic modeling using pseudosections showed that the orthopyroxene growth may have been triggered by water exsolution from the melt during ascent of xenoliths in basaltic magma. Euhedral-to-skeletal orthopyroxene growth probably reflects contrasting ascent rates of basaltic magma with xenoliths, intermitted by the stagnation in various crustal levels at a <3 kbar pressure. The Tertiary suite of intra-plate, mantle-derived A₁-type granites and syenites is geochemically distinct from pre-Tertiary, post-orogenic A₂-type granites of the Carpatho–Pannonian region, which exhibit geochemical features diagnostic of crustal melting along continental margins.     

Festkontaktierte potentiometrische Elektroden für Sulfatbestimmungen in wässrigen Lösungen

Solid‐contacted Potentiometric Electrodes for Measurements of Sulfate Ions in Aqueous Solutions A solid‐contact electrode for potentiometric measurement of sulfate ions in aqueous solutions was developed and examined. The electrode is based on a PVC membrane which contains the ionophore 3‐decyl‐1,5,8‐triazacyclodecan‐2,4‐dione (DTADD). Instead of the usual inner fluid junction, a polypyrrole layer applied on the inner side of the PVC membrane was employed as inner solid contact. The performance of this electrode was compared to solid‐state sulfate‐selective electrodes with the ionophore α,α′‐bis(N′‐phenylthioureylene)‐m‐xylene (BTH) and to electrodes in the coated‐wire configuration. For the parameters sensitivity, selectivity, and long‐term stability, electrodes with the DTADD ionophore show improved properties. In the sulfate concentration range of 5·10^–5...10^–2 mol L^–1 the slope of the response is –(26.8 ± 0.5) mV/decade. The new solid contact sulfate electrodes showed a very low drift of the electrode potential within a period of 150 days when the electrode was stored in 10^–2 M Na₂SO₄. In Na2SO4 solutions of the pH range of 4...9 the electrode potentials were constant. The 95% response time was about 10 s when the sulfate concentration was changed from 10^–4 mol L^–1 to 10^–3 mol L^–1. The selectivity with DTADD ionophore relating to the nitrate ions is higher than the selectivity with BTH. Improvements are also made in comparison with sulfate‐selective electrodes described in the literature which contain other ionophores with fluid inner reference electrolytes.     

High-resolution seabed imagery as a tool for biodiversity conservation planning on continental margins

Submarine canyons increase seascape diversity on continental margins and harbour diverse and abundant biota vulnerable to fishing. Because many canyons are fished, there is an increasing emphasis on including them in conservation areas on continental margins. Here we report on sponge diversity and bottom cover in three canyons of South-eastern Australia, test the performance of biological and abiotic surrogates, and evaluate how biological data from detailed seabed surveys can be used in conservation planning in these habitats. The biological data on sponge assemblage structure and species richness were obtained from 576 seafloor images taken between 148 and 472 m depth, yielding 65 morphospecies. Seafloor characteristics were similar within and between canyons, being almost exclusively composed of sediments with very few rocky substrates of higher relief. This environmental homogeneity did not, however, translate into biological uniformity of the megabenthos, and environmental factors were consequently poor predictors of biological features. By contrast, total bottom cover of sponges was highly correlated with species richness and served as a good proxy for species-level data in this situation. Design strategies that employ information on cover or richness of sponges provided a large dividend in conservation effort by dramatically reducing the number of spatial units required to achieve a specified conservation target of 50–90% of species to be included in reserves. This demonstrates that image-derived data are useful for the design of reserves in the deep sea, particularly where extractive sampling is not warranted. Using biological data on the sponge megabenthos to identify conservation units can also minimise socio-economic costs to fisheries because of a smaller geographic and bathymetric ambit of conservation areas.     

An automated full waveform logging system for high-resolution P-wave profiles in marine sediments

An automated, PC-based logging system has been developed to investigate marine sediment cores by full waveform transmission seismograms. High-resolution P-wave velocity and amplitude attenuation profiles are simultaneously derived from the transmission data to characterize the acoustic properties of the sediment column.A pair of ultrasonic, piezoelectric wheel probes is used to generate and record the transmission signals travelling radially through the sediment core. Both unsplit and split cores are allowed. Mounted in a carriage driven by a stepping motor via a shaft the probes automatically move along the core liner, stopping at equidistant spacings to provide a quasi-continuous inspection of the core by the transmission data. The axial travel distance and the core diameter are determined by digital measuring tools.First arrivals are picked automatically from the transmission seismograms using either a threshold in the seismogram's envelope or a cross-correlation algorithm taking the zero-offset signal of both wheel probes into account. Combined with the core diameter these first arrivals lead to a P-wave velocity profile with a relative precision of 1 to 2 m s^–1. Simultaneously, the maximum peak-to-peak amplitudes of the transmission seismograms are evaluated to get a first idea on the amplitude attenuation along the sediment core.Two examples of gravity cores taken during a recent cruise of R.V. METEOR in the Western Equatorial Atlantic are presented. They yield that the P-wave profiles can be used for locating strong and fine-scale lithological changes, e.g. turbidite layers and slight variations in the sand, silt or clay content. In addition, the transmission seismograms and their amplitude spectra obviously seem to reveal a correlation between the relative amount of low-frequency spectral components and the sediment grain size, and thus provide a tool for the determination of additional, related physical or sedimentological parameters in future investigations.     

17th International Cartographic Conference 10th General Assembly of ICA

Reports

17th International Cartographic Conference 10th General Assembly of ICA     

EPMA and PIXE dating of monazite in granulites from Stary Gierałtów, NE Bohemian Massif, Poland

Chemical Th–U–total Pb (CHIME) dating of monazite by electron probe microanalyzer (EPMA) and proton microprobe (PIXE) was carried out on felsic granulites from Stary Gierałtów, Poland, which represent part of the Orlica-Śnieżnik Dome in the NE Bohemian Massif. Analyzed monazite is characterized by mosaic zoning rather than simple core-to-rim growth, and strontium contents of up to 750ppm. An isochron age of 347 ± 13Ma represents timing of amphibolite-facies metamorphism, in agreement with previously published estimates.     

An Automated Iridium-Strip Heater for LA-ICP-MS Bulk Analysis of Geological Samples

In this paper we describe a flux‐free fusion technique for the highly precise LA‐ICP‐MS bulk analysis of geological samples. For this purpose we have developed an automated iridium‐strip heater with temperature and melt time control. To optimise the homogeneity of the fused glasses and to reduce possible depletion of volatile elements during melting, we undertook experiments with basaltic rock and glass powders using different melting temperatures (1300–1700 °C) and melting times (5‐80 s). Major and trace element microanalysis was performed using EPMA and LA‐ICP‐MS. Homogeneous glasses were obtained for temperatures ≥ 1500 °C and melting times ≥ 10 s. High loss (20‐90%) of highly volatile elements (e.g., Cs, Ge, Sn, Pb) was observed for high melting temperatures (≥ 1600 °C) and long melting times (80 s). Standard melting conditions (1600 °C, 10 s) represent a compromise, as the glasses were homogeneous with respect to major and trace elements and, at the same time, were not depleted in elements with condensation temperatures (at a pressure of 10^?4 bar) higher than about 900 K (e.g., Zr, Hf, Ba, Sr, REE, U, Mo, Ni, Rb, Ga). Several international geological reference materials with SiO₂ ranging between 47% m/m and 59% m/m were prepared using our standard melting conditions (1600 °C, 10 s) and subsequently analysed by LA‐ICP‐MS. These samples also include the new Brazilian basaltic reference material BRP‐1. Matrix‐matched calibration of the LA‐ICP‐MS data was performed using the basaltic reference glasses KL2‐G, ML3B‐G, BCR‐2G and BHVO‐2G. Most analytical data agreed within uncertainty at the 95% confidence level with the GeoReM preferred values published in the GeoReM database for reference materials of geological and environmental interest. To demonstrate routine bulk LA‐ICP‐MS analyses of geochemical and cosmochemical samples using the whole rock fusion technique, we also present trace element data for ocean island basalts from Lanai (Hawaii) and of Martian meteorites.