Orthogneisses of the Spessart crystalline complex,Northwest Bavaria: Indicators of the geotectonic environment?

The orthogneisses of the Spessart crystalline complex are derived from a granitic to granodioritic magma of S-type character which must have formed by anatexis of continental crust. It intruded into a relatively shallow crustal level, 410–420 Ma ago, at the Silurian. Trace element characteristics are consistent with a post-collision geotectonic environment testifying to extensional tectonics at the end of the Caledonian era.

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Zusammenfassung Die Orthogneise des Spessartkristallins lassen sich von einem granitischen bis granodioritischen Magma von S-Typ-Charakter ableiten, das durch Anatexis kontinentaler Kruste entstanden sein mu\ und in ein relativ oberflächennahes Krustenniveau intrudierte. Die Platznahme erfolgte vor 410–420 Ma, d. h. im Silur. Die Spurenelement-Muster der Orthogneise entsprechen denen von Post-Kollisions-Granitoiden, was als Hinweis auf eine Phase der Dehnungstektonik am Ende der kaledonischen ära bewertet werden kann.

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Résumé Les orthogneiss du Spessart sont dérivés d'un magma granitique à granodioritique de type S qui doit s'Être formé par anatexie de la croûte continentale. Ce magma a été intrudé dans un niveau peu profond de la croûte il y a 410–420 Ma c'est-à-dire au Silurien. La distribution des éléments en traces est en accord avec celle des granitoÏdes formés dans un contexte géodynamique de post-collision. Cette observation est en faveur d'une phase d'extension tectonique à la fin du cycle calédonien.

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Isotopic and hydrochemical studies of groundwater flow and salinity in the Southern Upper Rhine Graben

In order to determine the origin and the propagation mechanisms of highly concentrated chloride brines within the Quaternary aquifer system in the southern part of the Upper Rhine Graben, a combined isotope (H, O, C) and hydrochemical analysis was carried out. Groundwater recharge in this area is a complex system, consisting of local precipitation, river bank filtration, lateral flow from the Graben borders and, to a minor extent, an old Pleistocene component. In some areas, groundwater consists of up to 90% of recent bank filtrate, reaching depths down to at least 100 m. The isotopic and hydrochemical results show, that the elevated chloride concentrations in the Quaternary aquifer mainly result from leaky settling basins charged by the French potash mines until the mid 1970s. Input of natural brines coming from tertiary salt diapirs is of only minor importance. While infiltrating, the anthropogenic brines were strongly diluted by local river bank filtrate of the Rhine. Nevertheless, maximum chloride concentrations nowadays still reach some 10,000 mg/l at the base of the aquifer at a depth of more than 100 m below surface. The main volume of the brines is stored in the less permeable lower part of the quaternary sediments (Breisgau-Formation) whereas only a minor part is transported northwards with the rapid convective groundwater flow. Brines undergoing only dilution preserve their hydrochemical characteristics (NaCl-type). In contrast, brines recirculated from the Breisgau-Formation show a northwards increasing alteration through ion exchange processes. Potassium and sodium may be fixed in the fine grained aquifer material while calcium is set free into the groundwater. After a flow distance of about 12 km, complex hydraulic interactions between groundwater and surface waters lead to the rise of strongly diluted and hydrochemically altered brines with chloride contents up to maximum 700 mg/l. The presented case study is an example for a detailed analysis of a multi-component groundwater mixing system using combined isotope and hydrochemical methods. Furthermore, cation exchange is shown as a major process affecting the hydrochemical evolution of the young groundwater in the southern Upper Rhine Graben which is locally strongly polluted by chloride as a consequence of former potash mining.     

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Changes of cloud microphysical properties during the transition from supercooled to mixed-phase conditions during CIME

A ground-based seeding experiment using carbon dioxide and propane sprayed from pressurized bottles was carried out under supercooled cloud conditions on a small spatial and short time scale. Water vapor deposition on the artificially generated dry ice and propane ice germs as the main ice formation process (nucleation and growth) is consistent with the experimental results. After nucleation, diffusional growth of the ice particles, partly at the expense of evaporating small droplets, was identified during the mixing of the seeding line with the ambient supercooled cloud. Within the seeding plume, ice water contents up to 80% of the total condensed water are observed, although the size of the formed ice particles did not exceed 25 μm. From the changes of the ice and supercooled liquid phase with time under mixed-phase conditions, liquid water content (LWC) evaporation, ice water content (IWC) formation, and ice crystal growth rates are estimated, which are not affected by the artificial nucleation process. Thus, these rates are assessed to be applicable for a growing ice phase of small ice particles in a young mixed-phase cloud, where other growth mechanisms, like riming or aggregation, are negligible.     

Diagnosing southeast tropical Atlantic SST and ocean circulation biases in the CMIP5 ensemble

Warm sea-surface temperature (SST) biases in the southeastern tropical Atlantic (SETA), which is defined by a region from 5°E to the west coast of southern Africa and from 10°S to 30°S, are a common problem in many current and previous generation climate models. The Coupled Model Intercomparison Project Phase 5 (CMIP5) ensemble provides a useful framework to tackle the complex issues concerning causes of the SST bias. In this study, we tested a number of previously proposed mechanisms responsible for the SETA SST bias and found the following results. First, the multi-model ensemble mean shows a positive shortwave radiation bias of ~20 W m^?2, consistent with models’ deficiency in simulating low-level clouds. This shortwave radiation error, however, is overwhelmed by larger errors in the simulated surface turbulent heat and longwave radiation fluxes, resulting in excessive heat loss from the ocean. The result holds for atmosphere-only model simulations from the same multi-model ensemble, where the effect of SST biases on surface heat fluxes is removed, and is not sensitive to whether the analysis region is chosen to coincide with the maximum warm SST bias along the coast or with the main SETA stratocumulus deck away from the coast. This combined with the fact that there is no statistically significant relationship between simulated SST biases and surface heat flux biases among CMIP5 models suggests that the shortwave radiation bias caused by poorly simulated low-level clouds is not the leading cause of the warm SST bias. Second, the majority of CMIP5 models underestimate upwelling strength along the Benguela coast, which is linked to the unrealistically weak alongshore wind stress simulated by the models. However, a correlation analysis between the model simulated vertical velocities and SST biases does not reveal a statistically significant relationship between the two, suggesting that the deficient coastal upwelling in the models is not simply related to the warm SST bias via vertical heat advection. Third, SETA SST biases in CMIP5 models are correlated with surface and subsurface ocean temperature biases in the equatorial region, suggesting that the equatorial temperature bias remotely contributes to the SETA SST bias. Finally, we found that all CMIP5 models simulate a southward displaced Angola–Benguela front (ABF), which in many models is more than 10° south of its observed location. Furthermore, SETA SST biases are most significantly correlated with ABF latitude, which suggests that the inability of CMIP5 models to accurately simulate the ABF is a leading cause of the SETA SST bias. This is supported by simulations with the oceanic component of one of the CMIP5 models, which is forced with observationally derived surface fluxes. The results show that even with the observationally derived surface atmospheric forcing, the ocean model generates a significant warm SST bias near the ABF, underlining the important role of ocean dynamics in SETA SST bias problem. Further model simulations were conducted to address the impact of the SETA SST biases. The results indicate a significant remote influence of the SETA SST bias on global model simulations of tropical climate, underscoring the importance and urgency to reduce the SETA SST bias in global climate models.     

Compressional and shear wave velocities at high temperature and confining pressure in basalts from the Faeroe Islands

Compressional (V_P) and shear (V_S) wave velocities and the dependent elastic constants have been determined by the pulse transmission technique to 6 kb confining pressure at room temperature and to 700° C at 6 kb confining pressure for eleven basalts from the Faeroe Islands. The Faeroe basalts investigated are tholeiitic, they clearly lie within the tholeiitic area, and display a pronounced trend of iron enrichment from rocks with an M/M + F ratio of 0.5 to rocks with an M/M + F ratio of about 0.25. The mean V_P and V_S for eleven specimens are 5.57 km/sec and 3.18 km/sec, respectively. Velocity—density relations for the basalts might be more appropriately described by non-linear solutions than by linear relations commonly used for basalts. In general, V_P and V_S remain unaffected by temperature up to 300° C. At higher temperature the changes in wave velocities are influenced by metamorphic processes and are, therefore, somewhat erratic. In zeolite-bearing specimens an abrupt velocity decrease around 350°C is observed, which correlates well with a drastic compaction of bulk volume. Additional experiments on cold-pressed zeolite powder clearly indicate that the sharp velocity decrease in the basalts is related to dehydration of zeolite minerals. Partial-melting processes, which occur within vesicules and pore-spaces at distinctly higher temperatures have no additional effect on wave velocity. Comparison with field data reveals that, without exception, the velocities at 0.5 kb confining pressure display the same range that has been commonly noted in refraction data for Layer 2. There are no significant differences in wave velocities and the pressure—temperature dependence in samples recovered from the upper, middle, and lower basalt series in the Faeroe Islands.     

Silicon isotopic fractionation of CAI-like vacuum evaporation residues

Calcium-, aluminum-rich inclusions (CAIs) are often enriched in the heavy isotopes of magnesium and silicon relative to bulk solar system materials. It is likely that these isotopic enrichments resulted from evaporative mass loss of magnesium and silicon from early solar system condensates while they were molten during one or more high-temperature reheating events. Quantitative interpretation of these enrichments requires laboratory determinations of the evaporation kinetics and associated isotopic fractionation effects for these elements. The experimental data for the kinetics of evaporation of magnesium and silicon and the evaporative isotopic fractionation of magnesium is reasonably complete for Type B CAI liquids (Richter F. M., Davis A. M., Ebel D. S., and Hashimoto A. (2002) Elemental and isotopic fractionation of Type B CAIs: experiments, theoretical considerations, and constraints on their thermal evolution. Geochim. Cosmochim. Acta66, 521-540; Richter F. M., Janney P. E., Mendybaev R. A., Davis A. M., and Wadhwa M. (2007a) Elemental and isotopic fractionation of Type B CAI-like liquids by evaporation. Geochim. Cosmochim. Acta71, 5544-5564.). However, the isotopic fractionation factor for silicon evaporating from such liquids has not been as extensively studied. Here we report new ion microprobe silicon isotopic measurements of residual glass from partial evaporation of Type B CAI liquids into vacuum. The silicon isotopic fractionation is reported as a kinetic fractionation factor, α_Si, corresponding to the ratio of the silicon isotopic composition of the evaporation flux to that of the residual silicate liquid. For CAI-like melts, we find that α_Si = 0.98985 ± 0.00044 (2σ) for ²⁹Si/²⁸Si with no resolvable variation with temperature over the temperature range of the experiments, 1600-1900 °C. This value is different from what has been reported for evaporation of liquid Mg₂SiO₄ (Davis A. M., Hashimoto A., Clayton R. N., and Mayeda T. K. (1990) Isotope mass fractionation during evaporation of Mg₂SiO₄. Nature347, 655-658.) and of a melt with CI chondritic proportions of the major elements (Wang J., Davis A. M., Clayton R. N., Mayeda T. K., and Hashimoto A. (2001) Chemical and isotopic fractionation during the evaporation of the FeO-MgO-SiO₂-CaO-Al₂O₃-TiO₂-REE melt system. Geochim. Cosmochim. Acta65, 479-494.). There appears to be some compositional control on α_Si, whereas no compositional effects have been reported for α_Mg. We use the values of α_Si and α_Mg, to calculate the chemical compositions of the unevaporated precursors of a number of isotopically fractionated CAIs from CV chondrites whose chemical compositions and magnesium and silicon isotopic compositions have been previously measured.     

Crystallization of melilite from CMAS-liquids and the formation of the melilite mantle of Type B1 CAIs: Experimental simulations

Type B CAIs are subdivided into B1s, with well-developed melilite mantles, and B2s, with randomly distributed melilite. Despite intensive study, the origin of the characteristic melilite mantle of the B1s remains unclear. Recently, we proposed that formation of the melilite mantle is caused by depletion of the droplet surface in volatile magnesium and silicon due to higher evaporation rates of volatile species compared to their slow diffusion rates in the melt, thus making possible crystallization of melilite at the edge of the CAI first, followed by its crystallization in the central parts at lower temperatures. Here, we present the results of an experimental study that aimed to reproduce the texture observed in natural Type B CAIs. First, we experimentally determined crystallization temperatures of melilite for three melt compositions, which, combined with literature data, allowed us to find a simple relationship between the melt composition, crystallization temperature, and composition of first crystallizing melilite. Second, we conducted a series of evaporation and cooling experiments exposing CAI-like melts to gas mixtures with different oxygen fugacities (f_O2). Cooling of the molten droplets in gases with logf_O2?IW-4 resulted in crystallization of randomly distributed melilite, while under more reducing conditions, melilite mantles have been formed. Chemical profiles through samples quenched right before melilite started to crystallize showed no chemical gradients in samples exposed to relatively oxidizing gases (logf_O2?IW-4), while the near-surface parts of the samples exposed to very reducing gases (logf_O2?IW-7) were depleted in volatile MgO and SiO₂, and enriched in refractory Al₂O₃. Using these experimental results and the fact that the evaporation rate of magnesium and silicon from CAI-like melts is proportional to , we estimate that Type B1 CAIs could be formed by evaporation of a partially molten precursor in a gas of solar composition with . Type B2 CAIs could form by slower evaporation of the same precursors in the same gas with .