Über die Synthese von Albiten bei Temperaturen von 250 bis 700° C

A glass of composition NaAlSi₃O₈ with small contents of Fe has been crystallized in the presence of water vapor under 1000 bars, at temperatures in the range of 250 to 700° C for varying periods of time. The synthetic crystals were investigated microscopically and by x-ray powder diffraction methods. Most of the crystals are twinned according to the albite law, but other twins are found too. Size and form of the crystals seem to depend on the temperature of crystallization. The optic axial angles (2V _x ) of the albites being measurable on the universal stage are in the range of 50 to 100 degrees. There seems to exist a linear relation between the 2₁₃₁–2_1¯31 values (used as an indicator for the degree of ordering) and the 2V _x values. The change of the lattice parameters from albite (D) to albite (O) is suggested to deviate slightly from linearity.In contrast to previous investigations the steady value of 2₁₃₁–2_1¯31 which is characteristic of the temperature of crystallization was reached more rapidly. These results suggest that small content of Fe in the glass had a catalytic effect on the Al/Si ordering.

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Herrn Dr. F. Seifert (Ruhruniversität Bochum) danken wir herzlich für die Einweisung in die experimentellen Untersuchungsmethoden sowie für manchen kritischen Hinweis. Danken möchten wir auch Herrn Dr. P. K. Hörmann für die Kontrolle der chemischen Zusammensetzung des Albitglases sowie Herrn Dr. C. W. Burnham (Harvard University) für die Bereitstellung des Rechenprogramms. Nicht zuletzt danken wir Herrn Prof. Dr. F. Karl für die kritische Durchsicht des Manuskriptes.     

Towards an operational aqueous phase chemistry mechanism for regional chemistry-transport models: CAPRAM-RED and its application to the COSMO-MUSCAT model

Mechanism reductions of the detailed aqueous phase chemistry mechanism CAPRAM 3.0i are performed. Manual methods and automatic techniques are both applied in order to provide a less computationally intensive mechanism which is operational in regional chemistry transport models (CTMs). The finally reduced mechanism contains less than 200 reactions (4 times smaller than the detailed CAPRAM 3.0i) and describes the main characteristics of inorganic and organic aqueous phase processes occurring in tropospheric warm clouds. Most of the chemical reduction potential is realized in the CAPRAM 3.0i organic chemistry. The number of aqueous phase species decreases from 380 in the full mechanism to 130 in the final reduced version. The calculated percentage deviations between the full and reduced mechanism are on average below 5% for the most important organic and inorganic target compounds such as oxidants, inorganic and organic acids, carbonyls and alcohols. Comparisons of the required CPU times between the full and reduced mechanisms show reductions of approximately 40%. 2-D test simulations with the CTM MUSCAT were performed using prescribed meteorological conditions in order to examine the applicability of the reduced mechanism at regional scale. Simulations with the reduced CAPRAM 3.0i mechanism and a much less complex mechanism with only limited inorganic chemistry (INORG) were compared to evaluate the effects of more detailed chemistry. The model results show large differences in the level of oxidants and the inorganic and organic mass processing. Prospectively, the reduced mechanism represents the basis for studying aerosol cloud processing effects at regional scale with future CTMs and will allow more adequate interpretation of field data.     

Tantalite-(Mn) from the Borborema Pegmatite Province,northeastern Brazil: conditions of formation and melt- and fluid-inclusion constraints on experimental studies

Carbon dioxide-rich fluid and carbonate-rich aluminosilicate melt inclusions in tantalite-(Mn) from the Alto do Giz pegmatite in the Borborema Pegmatite Province, northeastern Brazil were investigated to constrain the formation of the host crystals. The results demonstrate that in the Alto do Giz pegmatite, water- and alkaline carbonate-rich fluids and melts are responsible for the transport and deposition of tantalite-(Mn) at temperatures around 600°C and about 4 kbar. Moreover, evidence is presented to show that during crystallization of the tantalite-(Mn), three different components coexisted, which are now trapped as separate inclusions: two immiscible silicate melts (types A and B melt inclusions) and a CO₂-rich aqueous fluid. We hypothesize that immiscible fluid separation may have been a critical factor in producing the water- and alkaline carbonate-rich fluids and melts necessary for Ta and Nb transport. Since the tantalite-(Mn) crystallized during pegmatite formation, this mechanism must also have implications for pegmatite genesis in general.     

Nitrate reduction potential of a fractured Middle Triassic carbonate aquifer in Southwest Germany

Hydrogeology Journal - Nitrate reduction constitutes an important natural mechanism to mitigate the widespread and persistent nitrate contamination of groundwater resources. In fractured aquifers,...     

Speciation of Trace Elements in Acidic PoreWaters from Waste Rock Dumps by Ultrafiltration andIon Exchange Combined with ICPMS and ICPOES

A speciation procedure developed on reactive acidicpore water samples from mining areas is presented.Methods with low consumption of solution are requiredthat allow rapid sample preparation to avoid equilibriumchanges as far as possible. The entire procedure includesonly three parallel separation steps. One aliquot is filteredthrough an 1 kd ultrafiltration membrane to separate traceelements adsorbed or complexed by colloids. One cationand one anion exchange are performed with two additionalaliquots to determine simple hydrated ions and smallinorganic complex ions. Commonly used procedures ofion exchange seem to be problematic. This new techniqueis based on a novel ion exchanger. Subsequently the threefractions obtained from the separation procedures and theoriginal pore water sample are analysed by ICPMS, ICPOES,ET-AAS, Flame-AAS, FES and IC to determine the concentrationsof the major ions and additionally up to 50 trace elements. Theinfluence of pH-values and several dissolved compounds iscontrolled in experiment series with synthetically preparedsolutions to reveal potential artifacts.     

Distribution of Crenarchaeota tetraether membrane lipids in surface sediments from the Red Sea

The Red Sea represents an extreme marine environment, with high salinity, high temperature and low level of nutrients, complicating the application of standard geochemical palaeotemperature proxies. In order to investigate the applicability of the TEX₈₆ (TetraEther indeX of GDGTs with 86 carbons) proxy for sea surface temperature (SST) in the Red Sea, the distribution of glycerol dialkyl glycerol tetraether membrane lipids (GDGTs) in sediments from the Red Sea and the Gulf of Aden were examined. Against expectations, TEX₈₆ values for the Red Sea do not show a simple linear relationship with SST and deviate from the global core top calibration. In the northern Red Sea, at temperatures between 25 and 28 °C, the values increase linearly with SST, whereas in the southern Red Sea, at temperatures above 28 °C, TEX₈₆ decreases with increasing temperature. Factors like seasonality and depth of production, salinity and nutrient availability, as well as diagenetic overprint or influence of allochtonous terrestrial lipids, cannot explain this pattern. However, the observed TEX₈₆ relationship with SST could be explained by the presence of a hypothetical endemic Crenarchaeota population in the Red Sea with a specific TEX₈₆ vs. SST relationship. In the Southern Red Sea, a two-component mixing model implies an exponential decrease in the endemic population towards the Gulf of Aden. Thus, the application of the TEX₈₆ as a palaeotemperature proxy in the Red Sea is likely only possible for the northern Red Sea area with the specific SST vs. TEX₈₆ relationship determined in this study and potentially for the whole Red Sea basin during glacials, when water exchange with the Indian Ocean was more restricted than today and the endemic archaeal lipid distribution was not affected by transport from the Indian Ocean. Our results suggest that distinct populations of Crenarchaeota in extreme environments such as evaporitic basins may have different membrane composition, necessitating application of another calibration than the global core top calibration for TEX₈₆ palaeothermometry.     

Sample return of interstellar matter (SARIM)

The scientific community has expressed strong interest to re-fly Stardust-like missions with improved instrumentation. We propose a new mission concept, SARIM, that collects interstellar and interplanetary dust particles and returns them to Earth. SARIM is optimised for the collection and discrimination of interstellar dust grains. Improved active dust collectors on-board allow us to perform in-situ determination of individual dust impacts and their impact location. This will provide important constraints for subsequent laboratory analysis. The SARIM spacecraft will be placed at the L2 libration point of the Sun–Earth system, outside the Earth’s debris belts and inside the solar-wind charging environment. SARIM is three-axes stabilised and collects interstellar grains between July and October when the relative encounter speeds with interstellar dust grains are lowest (4 to 20 km/s). During a 3-year dust collection period several hundred interstellar and several thousand interplanetary grains will be collected by a total sensitive area of 1 m². At the end of the collection phase seven collector modules are stored and sealed in a MIRKA-type sample return capsule. SARIM will return the capsule containing the stardust to Earth to allow for an extraction and investigation of interstellar samples by latest laboratory technologies.     

A note on Stokes production of turbulence kinetic energy in the oceanic mixed layer: observations in the Baltic Sea

Shear- and convection-driven turbulence coexists with wind-generated surface gravity waves in the upper ocean. The turbulent Reynolds stresses in the oceanic mixed layer can therefore interact with the shear of the wave-generated Stokes drift velocity to extract energy from the surface waves and inject it into turbulence, thus augmenting the mean shear-driven turbulence. Stokes production of turbulence kinetic energy (TKE) is difficult to measure in the field, since it requires simultaneous measurement of the turbulent stress and the Stokes drift profiles in the water column. However, it is readily inferred using second moment closure models of the oceanic mixed layer provided: (1) wave properties are available, along with the usual water mass properties, and radiative and air–sea fluxes needed to drive the mixed layer model and (2) the model skill can be assessed by comparing the model results against the observed dissipation rates of TKE. Comprehensive measurements made during the Reynolds 2002 campaign in the Baltic Sea have made the estimation of Stokes production possible, and in this paper, we report on the effort and the conclusions reached. Measurements of air–sea exchange parameters and water mass properties during the campaign allowed a mixed layer model to be run and the turbulent stress in the water column to be inferred. Simultaneous wave spectrum measurements enabled Stokes drift profile to be deduced and wave breaking to be included in the model run, and the Stokes production of TKE in the water column estimated. Direct measurements of the TKE dissipation rate from an upward traversing microstructure profiler were used to assure that the model could reproduce the turbulent dissipation rate in the water column. The model results indicate that the Stokes production of TKE in the mixed layer is of the same order of magnitude as the shear production and must therefore be included in mixed layer models.