Error in depth determination from resistivity soundings due to non-identification of suppressed layers

The magnitude of errors in the determination of depth to bedrock from Wenner and Schlumberger resistivity sounding curves, caused by the non-identification of a suppressed layer, has been investigated. The principal objective is to evaluate how the layer thicknesses and resistivities affect the accuracy of depth estimates. In the computations, the intermediate layer in a 3-layer model, in which the resistivity increases with depth, is removed and the 2-layer sounding curve that is electrically equivalent to the 3-layer curve is generated. The results indicate that there is a possibility for large depth underestimations when the resistivity contrast between layers 1 and 2 is very large. This is manifested in a steeply rising terminal branch on the sounding curve. There is a slight decrease in the depth underestimation as the resistivity contrast between layers 2 and 3 increases. Conversely, if the intermediate layer is fairly thick and the resistivity contrasts are not too large, the best-fit 2-layer curve shows large deviations from the 3-layer curve. In such cases, the intermediate layer can be identified, resulting in reliable depth estimates. A field example from Nigeria is presented in which the sounding data has been interpreted so as to account for a prebasement layer of intermediate resistivity, indicative of a fractured granite.     

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.     

A field comparison of indicators of sublethal stress in the salt-marsh grassSpartina patens

There is a need for research into bioindicators of stress in threatened plant communities such as coastal wetlands. Land subsidence, diversion of sediment, and salt-water intrusion produce stresses associated with waterlogging, elevated salinity, and nutrient depletion. Temporal and spatial environmental variation (soil redox potential, interstitial water salinity, pH, ammonium and phosphorus, and cation and trace metal concentrations) was analyzed near Lake de Cade, Louisiana, in a brackish marsh which is a mosaic of healthy plant communities interspersed with areas where wetland loss is occurring. Environmental variation was related to indicators of stress inSpartina patens, which included variables derived from the adenine nucleotide levels in plants, leaf spectral reflectance, leaf proline concentrations, and shoot elongation. In a comparison of burned and unburned sites, streamside and inland marsh, and along a salinity gradient, among-site differences were found in spectral reflectance and adenine-nucleotide-related indicators. Although it was difficult to relate a single causal environmental variable to the response of a specific indicator, spectral reflectance in the visible light range responded to salinity or to elements borne in seawater, and adenine-nucleotide indices were sensitive to nutrient availability. The ability of indicators to detect plant responses changed during the growing season, suggesting that they were responding to the changing importance of different environmental factors. In addition, some reflectance indicator responses occurred along salinity gradients when salinity differences were less than those that were found to have ecologically meaningful effects in greenhouse experiments. A multivariate numerical approach was used to relate environmental variation with indicator responses. We concluded that factors which in combination cause the degradation and loss of Louisiana wetlands produce environmental conditions that are only subtly different from those in vigorously growing marsh communities.     

Disequilibrium for Ca during growth of pelitic garnet

Compositional zoning in hundreds of almandine-rich garnets in amphibolite by facies micaceous quartzites from the Picuris Range, north-central New Mexico USA, indicates that although Mn, Mg and Fe achieve chemical equilibrium at hand-sample scale during garnet growth, Ca does not. Instead, Ca concentrations at the surface of growing garnets appear to depend strongly on kinetic factors that govern the local chemical environment, yielding disequilibrium for Ca at scales larger than the region immediately surrounding an individual porphyroblast. Detailed zoning profiles were obtained for 371 garnet crystals in a small volume of a single sample of garnetiferous quartzite, and core analyses were made of 97 additional crystals. Each analysis was made on a section that passed precisely through the morphological centre of the crystal, located by means of 3-D imagery from computed X-ray tomography. The data reveal strong correlations between crystal size and concentrations of Mn, Mg and Fe (but not Ca) in garnet cores; a relationship between crystal size and isolation; rigorous cross-correlations among concentrations of Mn, Mg and Fe (but not Ca); and systematic variations in Ca concentrations as a function of crystal size and core composition that are anomalous in comparison to the behaviour of the other divalent cations. We interpret these observations as the result of thermally accelerated diffusion-controlled garnet growth, in circumstances that promoted rapid intergranular diffusion and thus rock-wide equilibration of Mn, Mg and Fe, but that prevented equilibration at similar scale for Ca because of its more sluggish intergranular diffusion. The anomalous behaviour of Ca is made evident in these garnets by the presence of sharp spikes in Ca concentration, which are demonstrably not a consequence of any simultaneous rock-wide event, such as a change in pressure, temperature, or some other intensive parameter. Instead, Ca concentrations probably reflect the local extent of reaction in the immediate vicinity of each porphyroblast. To the degree that such kinetic factors introduce departures from chemical equilibrium for Ca, thermobarometric estimates that involve grossular contents of pelitic garnet will be in error.     

Comparison of source rock geochemistry of selected rocks from the Schei Point group and Ringnes formation, Sverdrup basin, arctic Canada

Organic-rich from the Schei Point group (middle to late Triassic in age) and the Ringnes formation (late Jurassic) from the Sverdrup basin of the Canadian arctic archipelago have been geochemically evaluated for source rock characterization. Most samples from the Schei Point group are organic-rich (> 2% TOC and are considered as immature to mature oil-prone source rocks [kerogen types I, I–II (IIA) and II (IIA)]. These kerogen types contain abundant AOM1, AOM2 and alginite (Tasmanales, Nostocopsis, Leiosphaeridia, acritarch and dinoflagellate) with variable amounts of vitrinite, inertinite and exinite. Samples from the Ringnes formation contain dominant vitrinite and inertinite with partially oxidized AOM2, alginite and exinite forming mostly immature to mature condensate- and gas-prone source rocks [kerogen type II–III (IIB), III and a few II (IIA)]. Schei Point samples contain higher bitumen extract, saturate hydrocarbons and saturate/ aromatic ratio than the Ringnes samples. Triterpane and sterane (dominant C₃₀) distribution patterns and stable carbon isotope of bitumen and kerogen suggest that the analyzed samples from the Schei Point group are at the onset of oil generation and contain a mixture of sapropelic (algal) and minor terrestrial humic organic matter. Sterane carbon number distributions in the Ringnes formation also suggest a mixed algal and terrestrial organic matter type. There are some variations in hopane carbon number distributions, but these are apparently a function of thermal maturity rather than significant genetic differences among samples. Pyrolysis-gas chromatography/mass spectrometry of the two samples with similar maturity shows that the Schei Point sample generates three times more pyrolyzate than the Ringnes sample. Both samples have a dominant aliphatic character, although the Ringnes sample contains phenol and an aromaticity that is higher than that of the Schei Point sample.     

Elasticity of tetragonal end-member majorite and solid solutions in the system Mg4Si4O12-Mg3Al2Si3O12

 The adiabatic elastic moduli of polycrystalline En₅₀Py₅₀ and En₈₀Py₂₀ majorite-garnet solid solutions (where En=4MgSiO₃, Py=Mg₃Al₂Si₃O₁₂) and the end-member En₁₀₀ tetragonal majorite were determined at ambient conditions using Brillouin spectroscopy. The adiabatic bulk modulus, K, and shear modulus, μ, of En₅₀Py₅₀ were found to be K=173.1 (20) and μ=92.3 (10) GPa, and are indistinguishable from those of the end-member pyrope, Py₁₀₀. The moduli of the more majorite-rich samples are significantly lower and are virtually identical to each other (K=162.6(11) and μ=85.7(7) for En₈₀Py₂₀; K=166(5) and μ=88(2) for En₁₀₀). In combination with previously reported moduli for this system, we conclude that both K and μ are constant over the compositional range from Py₁₀₀ to a majorite content of about 70–80%, whereupon the moduli decrease substantially. For compositions ranging from En₈₀Py₂₀ to the end-member majorite, the moduli are also approximately independent of composition, but at a lower value. An alternative model with a continuous decrease in moduli with increasing majorite content cannot be excluded, within the uncertainties of existing measurements. The contrast in moduli between aluminous pyrope garnet and Al-free majorite are small compared with the modulus changes accompanying the pyroxene – majorite phase transformation. Received August 16, 1995 /Revised, accepted January 12, 1996