Geochemistry of suspended matter from the Baltic Sea 2. Results of bulk trace metal analysis by AAS

In 1984, on a transect covering the whole Baltic Sea and parts of the adjacent North Sea, 160 water samples were taken and analysed for their concentrations of particulate and dissolved metals. In addition, the suspended materials were investigated for their elemental bulk composition.The particulate fractions represented from about 5% (Cd, Cu and Ni) to 50% (Fe and Pb) of the total (particulate plus dissolved) concentrations. For some elements (Ba, Cd, Cu, Pb and Zn), the particulate matter from the surface microlayer was enriched with respect to those suspended materials taken from 0.2 m depth. This could reflect the atmospheric input of metal-rich aerosols. In anoxic deep waters, maximum contents of Zn (6400 μg g⁻¹), Cu (1330 μg g⁻¹) and Cd (12 μg g⁻¹) were observed in the particulate matter, indicating sulphidic forms. On the other hand, under oxic conditions the distribution coefficients (K_d) decreased with the water depth (Cd, Fe and Pb).Relative to global background levels, the particulate matter contained metal “excesses” amounting to more than 90% of the total contents (Cd, Mn, Pb and Zn). Automated electron probe X-ray microanalysis (EPXMA) revealed that the elemental composition of sediments is mainly governed by post-depositional processes of early diagenesis and is only weakly related to the composition of suspended matter in the overlying water body. For instance, in relation to surface mud sediments of the central Baltic net-sedimentation basins, Zn, Cd, Cu and Mn had 30–100% higher levels in the suspended materials. The general pattern of metal contents of particulate matter taken from 10 m depth on a transect between the Bothnian Bay and the North Sea were—possibly as a result of anthropogenic inputs—rather similar for Pb, Zn and Cu. For Fe and Mn, the distribution patterns along the transect were probably governed by the natural loading characteristics and by the biogeochemistry of those elements.     

Zircon M257 ‐ a Homogeneous Natural Reference Material for the Ion Microprobe U‐Pb Analysis of Zircon

We introduce and propose zircon M257 as a future reference material for the determination of zircon U‐Pb ages by means of secondary ion mass spectrometry. This light brownish, flawless, cut gemstone specimen from Sri Lanka weighed 5.14 g (25.7 carats). Zircon M257 has TIMS‐determined, mean isotopic ratios (2s uncertainties) of 0.09100 ± 0.00003 for ²⁰⁶pb/²³⁸U and 0.7392 ± 0.0003 for ²⁰⁷pb/²³⁵U. Its ²⁰⁶pb/²³⁸U age is 561.3 ± 0.3 Ma (unweighted mean, uncertainty quoted at the 95% confidence level); the U‐Pb system is concordant within uncertainty of decay constants. Zircon M257 contains ～ 840 μg g^?1 U (Th/U ～ 0.27). The material exhibits remarkably low heterogeneity, with a virtual absence of any internal textures even in cathodoluminescence images. The uniform, moderate degree of radiation damage (estimated from the expansion of unit‐cell parameters, broadening of Raman spectral parameters and density) corresponds well, within the “Sri Lankan trends”, with actinide concentrations, U‐Pb age, and the calculated alpha fluence of 1.66 × 10¹⁸ g^?1. This, and a (U+Th)/He age of 419 ± 9 Ma (2s), enables us to exclude any unusual thermal history or heat treatment, which could potentially have affected the retention of radiogenic Pb. The oxygen isotope ratio of this zircon is 13.9%o VSMOW suggesting a metamorphic genesis in a marble or calc‐silicate skarn.     

A spectrophotometric measurement of soil cation exchange capacity based on cobaltihexamine chloride absorbance

Among numerous methods for cation exchange capacity (CEC) determination for soils and sediments, the cobaltihexamine chloride method is frequently used due to its ability to measure CEC at soil pH. After exchange with Co(NH₃)₆³⁺ ions, CEC is estimated via the measurement of the Co remaining in solution. The modified method proposed allows a more rapid determination of CEC based on the measurement of the absorbance at 472 nm of the cobaltihexamine chloride solution before and after exchange. This method has been applied to various soil's horizons from four sites, selected to cover a wide range of CEC and pH values. The model obtained allows one to calculate CEC from absorbance at 472 nm with 95% confidence intervals. As CEC is of relevant meaning in agronomical and environmental purposes, and more recently in ecotoxicological studies, this modified method can be proposed as a rapid test for CEC evaluation.     

Tracing the exhumation of the Eclogite Zone (Tauern Window,Eastern Alps) by <Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar dating of white mica in eclogites

New radiometric ages from the Subpenninic nappes (Eclogite Zone and Rote Wand – Modereck Nappe, Tauern Window) show that phengites formed under eclogite-facies metamorphic conditions retain their initial isotopic signature, even when associated lithologies were overprinted by greenschist- to amphibolite-facies metamorphism. Different stages of the eclogite-facies evolution can be dated provided ⁴⁰Ar/³⁹Ar dating is combined with micro-structural analyses. An age of 39 Ma from the Rote Wand – Modereck Nappe is interpreted to be close to the burial age of this unit. Eclogite deformation within the Eclogite Zone started at the pressure peak along distinct shear zones, and prevailed along the exhumation path. An age of ca. 38 Ma is only observed for eclogites not affected by subsequent deformation and is interpreted as maximum age due to the possible influence of homogenously distributed excess argon. During exhumation deformation was localised along distinct mylonitic shear zones. This stage is mainly characterised by the formation of dynamically recrystallized omphacite2 and phengite. Deformation resulted in the resetting of the Ar isotopic system within the recrystallized white mica. Flat argon release spectra showing ages of 32 Ma within mylonites record the timing of cooling along the exhumation path, and the emplacement onto the Venediger Nappe. Ar-release patterns and ³⁶Ar/⁴⁰Ar vs.³⁹Ar/⁴⁰Ar isotope correlation analyses indicate no significant ⁴⁰Ar-loss after initial closure, and only a negligible incorporation of excess argon. From the pressure peak onwards, eclogitic conditions prevailed for almost 8–10 Ma.     

Continuous injection model for hard X-ray correlated microwave bursts

Asymmetric magnetic field configurations in solar active regions hinder mildly relativistic electrons with magnetic moments suitable to produce microwave radiation from being trapped. Therefore the duration of stay of electrons in the microwave source region is much shorter (<0.2 s) than in the usually assumed trapping models. On this basis we construct a consistent model of hard X-ray correlated microwave bursts due to continuous injection of electrons into a pole field of an asymmetric magnetic loop (Figures 1 and 2). This resolves the discrepancy of the numbers of electrons needed to produce X-ray and radio emission.We compute gyrosynchrotron spectra with the assumption of conservation of the magnetic moment M in the microwave source. The consequence is an anticorrelation between the low frequency power index a of the microwave spectrum and the power index of the hard X-ray spectrum. In fact during the flare of May 18, 1972 increases with time while a is decreasing, so that +a= constant. Furthermore, it is shown that electrons with energies below 100 keV contribute significantly to the microwave radiation; they determine the low frequency spectrum completely.The model is able to explain the most often observed type C-spectra (Guidice and Castelli, 1975), but also flat spectra over one frequency decade.On leave from University of Berne, Institute of Applied Physics.