On the present habitats and ecology of Vertigo pseudosubstriata Ložek, 1954 (Mollusca,Gastropoda, Vertiginidea) in Central Asia and its distribution history in Central and Eastern Europe

The small terrestrial gastropod Vertigo pseudosubstriata Ložek, 1954 is one of the rarest glacial indicator species in the Pleistocene of Central and Eastern Europe. In all, this species has been found at only about 15 sites in Europe. V. pseudosubstriata was initially described as a fossil in Central Europe and was discovered only later alive in Central Asia. With regard to its modern distribution, 25 habitats with V. pseudosubstriata have been examined in Tien Shan and in the central and southern Altai. These findings seem to capture the contemporary distribution of the species and provide information on the boundaries of its ecological requirements. These data are of great significance for the interpretation of the fossil assemblages. Since the few fossil specimens in Europe date from very different glacial periods in the Elsterian, Saalian Complex and Weichselian, it can be concluded that V. pseudosubstriata apparently immigrated in at least three distinct waves. Most of the Pleistocene specimens in eastern Central Europe and Eastern Europe are reported from archaeological sites of the Upper Middle Weichselian (Gravettian), roughly between 33 and 29 ka cal bp. In this paper, we review all reported modern and fossil occurrences and discuss the species' ecological range.     

Molecular characterization of uranium(VI) sorption complexes on iron(III)-rich acid mine water colloids

A mixing of metal-loaded acid mine drainage with shallow groundwater or surface waters usually initiates oxidation and/or hydrolysis of dissolved metals such as iron (Fe) and aluminum (Al). Colloidal particles may appear and agglomerate with increasing pH. Likewise chemical conditions may occur while flooding abandoned uranium mines. Here, the risk assessment of hazards requires reliable knowledge on the mobility of uranium (U). A flooding process was simulated at mesocosm scale by mixing U-contaminated acid mine water with near-neutral groundwater under oxic conditions. The mechanism of U-uptake by fresh precipitates and the molecular structure of U bonding were determined to estimate the mobility of U(VI). Analytical and spectroscopic methods such as Extended X-ray Absorption Fine-Structure (EXAFS) spectroscopy at the Fe K-edge and the U L_III-edge, and Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) spectroscopy were employed. The freshly formed precipitate was identified as colloidal two-line ferrihydrite. It removed U(VI) from solution by sorption processes, while surface precipitation or structural incorporation of U was not observed. EXAFS data suggest a mononuclear inner-sphere, edge-sharing complex of U(VI) with ferrihydrite in the absence of dissolved carbonate. By employing a novel EXAFS analysis method, Monte Carlo Target Transformation Factor Analysis, we could for the first time ascertain a 3-D configuration of this sorption complex without the necessity to invoke formation of a ternary complex. The configuration suggests a slightly tilted position of the adsorbed unit relative to the edge-sharing Fe(O, OH)₆ octahedra. In the presence of dissolved carbonate and at pH ∼8.0, a distal carbonate O-atom at ∼4.3 Å supports formation of ternary U(VI)-carbonato surface complexes. The occurrence of these complexes was also confirmed by ATR-FTIR. However, in slightly acidic conditions (pH 5-6) in equilibrium with atmospheric CO₂, the U(VI) sorption on ferrihydrite was dominated by the binary complex species Fe(O)₂UO₂, whereas ternary U(VI)-carbonato surface complexes were of minor relevance. While sulfate and silicate were also present in the mine water, they had no detectable influence on U(VI) surface complexation. Our experiments demonstrate that U(VI) forms stable inner-sphere sorption complexes even in the presence of carbonate and at slightly alkaline pH, conditions which previously have been assumed to greatly accelerate the mobility of U(VI) in aqueous environments. Depending on the concentrations of U(VI) and carbonate, the type of surface complexes may change from binary uranyl-ferrihydrite to ternary carbonato-uranyl-ferrihydrite complexes. These different binding mechanisms are likely to influence the binding stability and retention of U(VI) at the macroscopic level.     

Storm-related sea level variations along the North Sea coast as simulated by a high-resolution model 1958–2002

Storm-related sea level variations 1958–2002 along the North Sea coast from a high-resolution numerical hindcast are investigated and compared to the results of earlier studies. Considerable variations were found from year to year and over the entire period. The large-scale pattern of these variations is consistent with that derived from previous studies, while the magnitudes of the long-term trends differ. The latter is attributed to different analysis periods, improvements in the atmospheric forcing, and the enhanced spatial resolution of the numerical simulation. It is shown that the different analysis periods, in particular, represent an issue as the increase in storm-related sea levels was found to be weaker over the last few years that have not been included in earlier studies. These changes are consistent with observed changes of the storm climate over the North Sea. It is also shown that observed and hindcast trends may differ significantly. While the latter are in agreement with observed changes in the storm climate, it may be concluded that observed sea level changes along the North Sea coast comprise a considerable fraction that cannot be attributed to changes in the large-scale atmospheric circulation.

Ice crystal shape effects on solar radiative properties of Arctic mixed-phase clouds—Dependence on microphysical properties

Based on 1-year cloud measurements with radar and microwave radiometer broadband solar radiative transfer simulations were performed to quantify the impact of different ice crystal shapes of Arctic mixed-phase clouds on their radiative properties (reflectance, transmittance and absorptance). The ice crystal shape effects were investigated as a function of microphysical cloud properties (ice volume fraction f_i, ice and liquid water content IWC and LWC, mean particle diameter D_m^I and D_m^W of ice/water particle number size distributions, NSDs).The required NSDs were statistically derived from radar data. The NSD was composed of a liquid and a solid mode defined by LWC, D_m^W (water mode) and IWC, D_m^I (ice mode). It was found that the ratio of D_m^I and D_m^W determines the magnitude of the shape effect. For mixed-phase clouds with D_m^I ≤ 27 μm a significant shape effect was obtained. The shape effect was almost insensitive with regard to the solar zenith angle, but highly sensitive to the ice volume fraction of the mixed-phase cloud. For mixed-phase clouds containing small ice crystals (D_m^I ≤ 27 μm) and high ice volume fractions (f_i > 0.5) crystal shape is crucial. The largest shape effects were observed assuming aggregates and columns. If the IWC was conserved the shape effect reaches values up to 0.23 in cloud reflectance and transmittance. If the ice mode NSD was kept constant only a small shape effect was quantified (≤ 0.04).     

Theoretical considerations on the mass and energy consistent treatment of precipitation in cloudy atmospheres

The purpose of this paper is to present a rigorous derivation of a model equation system for the mass and energy open precipitating atmosphere. The derivation is based on the treatment of the atmosphere in terms of three open thermodynamic subsystems consisting of cloudy air, rain water and snow, respectively. Each of the three subsystems moves with a different velocity as caused by the different fall velocities of rain and snow in comparison to the cloudy air.A basic assumption of the model consists in the neglect of the inertia terms in the momentum equation of the falling hydrometeors. It will be shown that this simplification yields additional source terms in the budget equations of the total momentum and the total kinetic energy of the system. However, the prognostic equations for the atmospheric wind field and the corresponding kinetic energy equation remain free of these source terms. The model equations strictly conserve the total mass and energy of the system. It is concluded that the combination of the barycentric velocity of the cloudy air and the total density of the system is the best choice to describe the time evolution of the atmospheric wind field.     

On Reynolds Averaging of Turbulence Time Series

We show that validity of Reynolds averaging for estimating the (ensemble) mean of a turbulence time series requires that the series values be both stationary and uncorrelated. In strict statistical terminology, these two conditions are jointly designated as independent identically distributed (i.i.d.). Moreover, we show that when the series values are correlated, knowledge of the correlation between the values is needed to obtain a reliable estimate of the mean. Last, we contend that a viable averaging algorithm must be Reynolds number (Re) dependent, requiring one version for low Re (Gaussian) turbulence and another for high Re (non-Gaussian) turbulence. Alternatively the median (as opposed to the mean) is recommended as a measure of the central tendency of the turbulence probability density function.     

Li-bearing, disordered Mg-rich tourmaline from a pegmatite-marble contact in the Austroalpine basement units (Styria, Austria)

Pale-blue to pale-green tourmalines from the contact zone of Permian pegmatites to mica schists and marbles from different localities of the Austroalpine basement units (Rappold Complex) in Styria, Austria, are characterized. All these Mg-rich tourmalines have small but significant Li contents, up to 0.29 wt% Li₂O, and can be characterized as dravite, with FeO contents of ?~?0.9–2.7 wt%. Their chemical composition varies from ^X (Na_0.67Ca_0.19?K_0.02?_0.12) ^Y (Mg_1.26Al_0.97Fe²⁺ _0.36Li_0.19Ti⁴⁺ _0.06Zn_0.01?_0.15) ^Z (Al_5.31?Mg_0.69) (BO₃)₃ Si₆O₁₈ ^V (OH)₃? ^W [F_0.66(OH)_0.34], with a?=?15.9220(3), c?=?7.1732(2) Å to ^X (Na_0.67Ca_0.24?K_0.02?_0.07) ^Y (Mg_1.83Al_0.88Fe²⁺ _0.20Li_0.08Zn_0.01Ti⁴⁺ _0.01?_0.09) ^Z (Al_5.25?Mg_0.75) (BO₃)₃ Si₆O₁₈ ^V (OH)₃? ^W [F_0.87(OH)_0.13], with a?=?15.9354(4), c?=?7.1934(4) Å, and they show a significant Al-Mg disorder between the Y and the Z sites (R1?=?0.013–0.015). There is a positive correlation between the Ca content and?<?Y-O?>?distance for all investigated tourmalines (r?≈?1.00), which may reflect short-range order configurations including Ca and Fe²⁺, Mg, and Li. The tourmalines have X_Mg (X_Mg?=?Mg/Mg?+?Fe_total) values in the range 0.84–0.95. The REE patterns show more or less pronounced negative Eu and positive Yb anomalies. In comparison to tourmalines from highly-evolved pegmatites, the tourmaline samples from the border zone of the pegmatites of the Rappold Complex contain relatively low amounts of total REE (~8–36 ppm) and Th (0.1–1.8 ppm) and have low La_N/Yb_N ratios. There is a positive correlation (r?≈?0.91) between MgO of the tourmalines and the MgO contents of the surrounding mica schists. We conclude that the pegmatites formed by anatectic melting of mica schists and paragneisses in Permian time. The tourmalines crystallized from the pegmatitic melt, influenced by the metacarbonate and metapelitic host rocks.     

Zircon texture and chemical composition as a guide to magmatic processes and mixing in a granitic environment and coeval volcanic system

This study documents the chemical and textural responses of zircon in the Elba igneous complex, with particular reference to the 7- to 7.8-Ma-old Monte Capanne pluton in relation to its coeval volcanic counterpart (Capraia), using BSE imaging and quantitative electron microprobe analyses. The Monte Capanne pluton displays multiple field and geochemical evidence for magma mixing. The samples we have investigated (including monzogranitic, mafic enclave and dyke samples) display similar zircon textures and are associated with an extremely large range of trace and minor element (Hf, Y, HREE, Th, U) compositions, which contrast with relatively simple textures and zoning patterns in zircons from a Capraia dacite. We have used a relatively simple textural classification (patchy zoning, homogenous cores, oscillatory zoning and unzoned zircon) as the basis for discussing the chemical composition and chemical variation within zircons from the Monte Capanne pluton. Based on these data and other works (Dini et al. 2004 in Lithos 78:101–118, 2004) , it is inferred that mixing between metaluminous and peraluminous melts occurred early in the evolution of the Monte Capanne magma chamber. In particular, mixing was responsible for the development of the patchy-zoning texture in the zircon cores, which was associated with reactions between other accessory phases (including monazite, apatite, allanite), which we infer to have significantly affected the Th distribution in zircon. Zircons from the MC pluton displaying “homogeneous cores” have chemical affinities with zircons in the coeval Capraia volcanic system, consistent with the participation of a Capraia-like mantle end-member during mixing. Further zircon growth in the MC pluton produced the oscillatory zoning texture, which records both long-term (crystal fractionation) and transient (recharge with both silicic and mafic magmas) events in a hybrid magma chamber. It is inferred that Hf and the Th/U ratio cannot be used alone to infer magmatic processes due to their dependency on temperature, nor are they a diagnostic feature of xenocrystic grains. This study shows that zircon chemistry coupled with detailed textural analysis can provide a powerful tool to elucidate the complex evolution of a magma system.     

CO2 sequestration and extreme Mg depletion in serpentinized peridotite clasts from the Devonian Solund basin, SW-Norway

The conglomerates of the Solund Devonian basin of SW-Norway contain numerous (locally up to 20 vol.%) peridotitic clasts with concentric mm- to 10-cm thick zones of varying red to black color. The peridotite clasts show a clear, alteration-related textural evolution. The least-altered rocks are partly serpentinized peridotites, showing a typical mesh texture with veins of serpentine, magnesite and Ni-rich magnetite surrounding olivine (Fo₉₁) relicts and its Mg-depleted, clay-like alteration product (deweylite assemblage). In the more advanced ophicarbonate stage, the mesh cells contain calcite, silica and are surrounded by talc. In the final stage, quartz, calcite, and hematite dominate the mineralogy and occur together with minor amounts of chromite, talc, Cr-chlorite, and Cr-hydroandradite. In tandem with this textural evolution is a decrease in MgO from 40 to 2.5 wt% and a CaO increase from 1 to 35 wt%. All peridotite clasts are characterized by high Cr and Ni concentrations. The chemistry and the textural evolution show that the clasts formed by an extreme Mg-mobilization from the peridotite, with development of secondary porosity and subsequent precipitation of calcite. MgO removed from the clasts after burial is in part consumed by replacement reactions in the sediment matrix around the clasts where Mg-free minerals (e.g., almandine) are replaced by Mg-bearing minerals (e.g., talc). Calculated apparent ⁸⁷Sr/⁸⁶Sr ratios of the clasts at 385 Ma (0.7124-0.7139), corresponding to the inferred age of sediment deposition and incipient clast alteration, indicate interaction with diagenetic basinal fluids. We explain the reaction history as a three stage process involving (a) partial serpentinization of olivine in an oceanic environment (b) breakdown of olivine relicts to the deweylite assemblage resulting in mobilization of MgO under (near-) surface conditions in a tropical Devonian climate and (c) further Mg-mobilization and replacement of the deweylite assemblage by calcite and quartz after diagenesis. Sedimentary basins with abundant weathered peridotite represent potential sites for a permanent CO₂ storage by formation of calcite in a low-temperature environment.     

Synthetic stellar and SSP libraries as templates for Gaia simulations

ESA’s Gaia mission will collect low resolution spectroscopy in the optical range for ～10⁹ objects. Complete and up-to-date libraries of synthetic stellar spectra are needed to built algorithms aimed to automatically derive the classification and the parametrization of this huge amount of data. In addition, libraries of stellar spectra are one of the main ingredients of stellar population synthesis models, aiming to derive the properties of unresolved stellar populations from their integrated light. We present (a) the newly computed libraries of synthetic spectra built by the Gaia community, covering the whole optical range (300–1100 nm) at medium-high resolution of (0.3 nm) for stars spanning the most different types, from M to O, from A-peculiar to Emission lines to White Dwarfs, and (b) the implementation of those libraries in our SSP code (Tantalo in The Initial Mass Function 50 Years Later, 327:235 2005), exploring different stellar evolution models.