Geomorphological models as a tool for environmental studies

Relief is understood as a fundamental component of the environmental system. The structure of geomorphodynamic processes and of the relief sphere as the main energy transformation surface is a determining factor for environmental conditions of both sites and areas. Modelling is the instrument of the applied and systems analytic approach to geomorphology. Geomorphological tools are appropriate means of determining, structuring, assessing and predicting the geoecological potential of the environment. This is demonstrated by quantitative and multivariate models to describe spatial patterns of the environment (fluvial network analysis) and to evaluate and present environmentally relevant geomorphological disposition (slope stability analysis).     

Water in garnet of garnetite (metarodingite) and eclogite from the Erzgebirge and the Lepontine Alps

Little is known about water in nominally anhydrous minerals of orogenic garnet peridotite and enclosed metabasic rocks. This study is focused on peridotite-hosted eclogite and garnetite (metarodingite) from the Erzgebirge (EG), Germany, and the Lepontine Alps (LA), Switzerland. Newly discovered, peridotite-hosted eclogite in the Erzgebirge occurs in the same ultra-high pressure (UHP) unit as gneiss-hosted coesite eclogite, from which it is petrologically indistinguishable. Garnet is present in all mafic and ultramafic high pressure (HP) rocks providing for an ideal proxy to compare the H₂O content of the different rock types. Garnet composition is very similar in EG and LA samples and depends on the rock type. Garnet from garnetite, compared to eclogite, contains more CaO (garnetite: 10.5–16.5 wt%; eclogite: 5–11 wt%) and is also characterized by an anomalous REE distribution. In contrast, the infrared (IR) spectra of garnet from both rock types reveal the same OH absorption bands that are also identical to those of previously studied peridotitic garnet from the same locations. Two groups of IR bands, SW I (3,650 ± 10 cm⁻¹) and SW II (3,570–3,630 cm⁻¹) are ascribed to structural hydroxyl (colloquially ‘water’). A third, broad band is present in about half of the analysed garnet domains and related to molecular water (MW) in submicroscopic fluid inclusions. The primary content of structural H₂O, preserved in garnet domains without fluid inclusions (and MW bands), varies systematically—depending on both the location and the rock type. Garnet from EG rocks contains more water compared to LA samples, and garnet from garnetite (EG: 121–241 wt.ppm H₂O; LA: 23–46 wt.ppm) hosts more water than eclogitic garnet (EG: 84 wt.ppm; LA: 4–11 wt.ppm). Higher contents of structural water (SW) are observed in domains with molecular water, in which the SW II band (being not restricted to HP conditions) is simultaneously enhanced. This implies that fluid influx during decompression not only led to fluid inclusions but also favoured the uptake of secondary SW. The results signify that garnet from all EG and LA samples was originally H₂O-undersaturated. Combining the data from eclogite, garnetite and previously studied peridotite, H₂O and CaO are positively correlated, pointing to the same degree of H₂O-undersaturation at peak metamorphism in all rock types. This ubiquitous water-deficiency cannot be reconciled with the derivation of any of these rocks from the lowermost part of the mantle wedge that was in contact with the subducting plate. This agrees with the previously inferred abyssal origin for part of the rocks from the LA (Cima di Gagnone). A similar origin has to be invoked for the Erzgebirge UHP unit. We suggest that all mafic and ultramafic rocks of this unit not only shared the same metamorphic evolution but also a common protolith origin, most probably on the ocean floor. This inference is supported by the presence of peridotite-hosted garnetite, representing metamorphosed rodingite.     

Geochronology,stratigraphy and geochemistry of Cambro-Ordovician,Silurian and Devonian volcanic rocks of the Saxothuringian Zone in NE Bavaria (Germany)—new constraints for Gondwana break up and ocean–island magmatism

International Journal of Earth Sciences - Stratigraphically well-defined volcanic rocks in Palaeozoic volcano-sedimentary units of the Frankenwald area (Saxothuringian Zone, Variscan Orogen) were...     

Experimental investigation of the metamorphism of siliceous dolomites

For the reaction: 1 diopside+3 dolomite ?2 forsterite+4 calcite+2 CO₂ (14) the following P _total?T-brackets have been determined experimentally in the presence of a gasphase consisting of 90 mole%CO₂ and 10 mole%H₂O∶1 kb, 544°±20° C; 3kb, 638°±15° C; 5kb, 708°±10° C; 10kb, 861°±10° C. The determination was carried out with well defined synthetic minerals in the starting mixture. The MgCO₃-contents of the magnesian calcites formed by the reaction in equilibrium with dolomite agree very well with the calcite-dolomite miscibility gap, which can be recalculated from the activities and the activity coefficients of MgCO₃ as given by Gordon and Greenwood (1970). The equilibrium constant K _14b was calculated with respect to the reference pressure P ₀=1 bar using the experimentally determined \(P_{total} TX_{CO_2 }\) brackets, the activities of MgCO₃ and CaCO₃ (Gordon and Greenwood 1970; Skippen 1974) and the fugacities of CO₂ Holloway (1977) considering the correction of Flowers (1979). Results are plotted as function of the absolute reciprocal temperature in Fig. 1. For the temperature range of 530° to 750° C the following linear expression can be given for the natural logarithm of K_14b: (g) $$[ln K_{14b} ]_T^P = - \frac{{18064.43}}{{T\left( {^\circ K} \right)}} + 38.58 + \frac{{0.308(P - 1 bar)}}{{T\left( {^\circ K} \right)}}$$ where P is the total pressure in bars and T the temperature in degrees Kelvin. Combining Equation (g) with the activities of MgCO₃ and CaCO₃ gives the equilibrium fugacity \(f_{CO_2 }\) : (i) $$[ln f_{CO_2 } ]_T^P = - \frac{{11635.44}}{{T\left( {^\circ K} \right)}} + 21.09 + \frac{{0.154(P - 1 bar)}}{{T\left( {^\circ K} \right)}}$$ Equation (i) and the fugacities of CO₂ permit to calculate the equilibrium data in terms of \(P_{CO_2 }\) and T (see Fig. 3) or P _total, T and \(X_{CO_2 }\) (see Fig. 5). Combining the \(P_{total} TX_{CO_2 }\) equilibrium data of the above reaction with those of the previously investigated reaction (Metz 1976): 1 tremolite+11 dolomite ?8 forsterite+13 calcite+9 CO₂+1 H₂O yields the stability conditions of the four-mineral assemblage: diopside+calcian dolomite+forsterite +magnesian calcite and the stability conditions of the five-mineral assemblage: tremolite+calcian dolomite+forsterite +magnesian calcite+diopside both shown in Fig. 6. Since these assemblages are by no means rare in metamorphic siliceous dolomites (Trommsdorff 1972; Suzuki 1977; Puhan 1979) the data of Fig. 6 can be used to determine the pressure of metamorphism and to estimate the composition of the CO₂-H₂O fluid provided the temperature of the metamorphic event was determined using the calcite-dolomite geothermometer.     

Late Pleistocene fluvial dynamics in the Hochrhein Valley and in the Upper Rhine Graben: chronological frame

During the Pleistocene, the Rhine glacier system acted as a major south–north erosion and transport medium from the Swiss Alps into the Upper Rhine Graben, which has been the main sediment sink forming low angle debris fans. Only some aggradation resulted in the formation of terraces. Optically stimulated luminescence (OSL) and radiocarbon dating have been applied to set up a more reliable chronological frame of Late Pleistocene and Holocene fluvial activity in the western Hochrhein Valley and in the southern part of the Upper Rhine Graben. The stratigraphically oldest deposits exposed, a braided-river facies, yielded OSL age estimates ranging from 59.6 ± 6.2 to 33.1 ± 3.0 ka. The data set does not enable to distinguish between a linear age increase triggered by a continuous autocyclical aggradation or two (or more) age clusters, for example around 35 ka and around 55 ka, triggered by climate change, including stadial and interstadial periods (sensu Dansgaard–Oeschger cycles). The braided river facies is discontinuously (hiatus) covered by coarse-grained gravel-rich sediments deposited most likely during a single event or short-time period of major melt water discharge postdating the Last Glacial Maximum. OSL age estimates of fluvial and aeolian sediments from the above coarse-grained sediment layer are between 16.4 ± 0.8 and 10.6 ± 0.5 ka, and make a correlation with the Late Glacial period very likely. The youngest fluvial aggradation period correlates to the beginning of the Little Ice Age, as confirmed by OSL and radiocarbon ages.     

Die lokale Beeinflussung eines stehenden Gewässers durch eine punktförmige Abwasserbelastung; ein direkter Nachweis der wachstumsbegrenzenden Wirkung des Phosphors im Vierwaldstättersee

Zusammenfassung Die Beeinflussung des Vierwaldst?ttersees (Horwer Bucht) durch den mit dem Abwasser von 10 000 Einwohnern belasteten Steinibach liess sich im Oberfl?chenwasser auf eine Distanz von mehr als 2 km verfolgen (Abb. 1a, 1b, 1c). Es zeigte sich, dass eine erh?hte Phosphorzufuhr eine verst?rkte biogene Nitratzehrung erm?glicht. Die Abh?ngigkeit der Pigmentkonzentration y von der Gesamtphosphorkonzentrationx liess sich durch die folgende Mitscherlich-Gleichung beschreiben: log(30-y)=log 30–0,012 (x−6) Damit wurde im Vierwaldst?ttersee erstmals unter v?llig natürlichen Bedingungen die Beeinflussung der Prim?rproduktion durch eine erh?hte Phosphorkonzentration nachgewiesen (Abb. 2). Die Erfolgsaussichten von Abwassersanierungsmassnahmen an Seen verschiedener Trophiegrade werden diskutiert.

---

Summary The influence of the ‘Steinibach” tributary, into which the wastewater of 10,000 inhabitants is discharged, on the Lake of Lucerne (Horwer Bucht) is detectable in the surface water over a distance of more than 2 km (Picture 1a, 1b, 1c). It was revealed that the increased phosphorus supply enables more intensive biological nitrate consumption. The dependence of the pigment concentration,y, on the total phosphorus concentration,x can be expressed by the following Mitscherlich equation: log (30−y)=log 30–0.012 (x−6). This was the first time that the influence of an increased phosphorus concentration on primary production was proved in the Lake of Lucerne under completely natural conditions (Picture 2). The possibilities of implementing successful water pollution control measures in lakes with various trophic levels are discussed.

     

Exhumed fault-bounded Alpine blocks along the Periadriatic lineament: the Eder unit (Carnic Alps, Austria)

The Eder unit in the Carnic Alps, which is situated immediately south of the Periadriatic lineament (PL), represents a fault-bounded block consisting of a low-grade (up to 400?°C, indicated by epizonal illite “crystallinity” values, recrystallized quartz, and non-recrystallized white mica) metamorphic Paleozoic metasedimentary sequence. Until now, it has been assumed to represent a separate Variscan nappe. The rocks of the Eder unit show a strong E- to W-oriented stretching lineation on steep foliation planes (D₁) subparallel to the PL. D₁ structures originated near the temperature peak of metamorphism, and shear sense indicators show dextral ductile shear parallel to the PL. Tight mesoscale D₂ folds formed on the cooling path. K–Ar and Ar–Ar ages from newly formed white mica cluster around 32–28 and 18–13 Ma and suggest a two-stage Tertiary history of the Eder unit. We interpret the Eder unit as a fault-bounded block formed during Oligocene large-scale dextral shearing along the PL (near T_max) and exhumed in mid-Miocene times during another phase of activity along the PL. Its nature as a separate Variscan nappe is questioned.     

Une approche innovante pour modéliser la biodégradation des composés organochlorés volatils en aquifères poreux

The goal of this study was to develop an innovative chloroethene biodegradation module based on biological, thermodynamical and mechanistic concepts. The biodegradation scheme was based on the postulate that in each part of an aquifer only one degradation mechanism is dominant: the one involving the most energetic electron acceptor. Thus, the selection of the active degradation mechanism was a function of the concentration of different electron acceptors. Modified Monod-type kinetics was used in order to take into account the possible influence of some compounds on the biodegradation of a given organic compound. The numerical model developed was applied to a simple test case, whose results are presented here. To cite this article: F. Nex et al., C. R. Geoscience 338 (2006).