Nouvelle interprétation structurale de la « faille Nord- Pyrénéenne » en vallée d'Aspe (Pyrénées-Atlantiques). Remise en question d'un plutonisme ophitique danien dans le secteur de Bedous

In the Aspe Valley (western Pyrenees), the Europe/Iberia boundary corresponds to a complex fracturing zone, called the ‘Bielle–Accous Wrench-Faulting Corridor’, which represents the classical ‘North-Pyrenean Fault’. Located between the High Primary Range and the North-Pyrenean Zone, the BAWC shows different south-verging sheets mainly composed of Triassic materials. The Bedous ophite, associated with Muschelkalk and Keuper sediments, is also Triassic in age and involved in the same Pyrenean thrusting structures. So, contrary to a recent interpretation, this magmatic rock cannot be related to a supposed Danian plutonism inducing metamorphic processes in the surrounding Mesozoic formations. To cite this article: J. Canérot et al., C. R. Geoscience 336 (2004).     

Nickel, Copper, Zinc and Cadmium Cycling with Manganese in Lake Vanda (Wright Valley, Antarctica)

Lake Vanda is a closed-basin, permanently ice-covered lake located in the Wright Valley of Antarctica. The lakes more important geochemical features include the fact that it is fed by a single glacial melt water stream for only 6–8weeks out of the year; that it has remained stratified for more than a millennium; and that, like other lakes in the region, it is remote from anthropogenic influence. These, together with the fact that it is among the least biologically productive lakes in the world, make it an ideal system for examining the transport, cycling and fate of trace metals in the aquatic environment. Like others before us, we view this lake as a natural geochemical laboratory, a flask in the desert. This paper presents the first set of closely spaced, vertical, profiles for dissolved and particulate Mn, Fe, Ni, Cu, Zn and Cd in the water column. Despite the absence of an outflow, metals in the fresh upper waters of the lake have extremely low concentrations, in the pico-molar to nano-molar range, and are partitioned largely into dissolved rather than particulate phases. Efficient metal scavenging by particles from these oxygen-rich waters is indicated. Significant increases in metal concentrations begin to appear at depth, between 57 and 60m, and these increases coincide with the onset of manganese oxide dissolution in oxic, but lower pH waters. Vertical profiles suggest that the entire suite of trace metals (Ni, Cu, Zn, and Cd) is being released from manganese oxide carrier phases. Thermodynamic analysis indicates that Mn3O4 (i.e., the mineral hausmannite) may be important in metal sequestration and recycling in the deeper waters of Lake Vanda. Manganese-reducing organisms reported by Bratina etal. (1998) are active in the zone of metal release and these could also contribute to the observed cycling.     

A high-resolution TEM-AEM, pH titration, and modeling study of Zn coprecipitation with ferrihydrite

Experiments of Zn²⁺ and Fe³⁺ coprecipitation as a function of pH were conducted in the laboratory at ambient temperature and pressure. X-ray diffraction patterns of the coprecipitates show two broad peaks at 0.149 and 0.258 nm, which is consistent with published patterns for pure 2-line ferrihydrite. Zn²⁺ uptake occurred at pH ≥5 while Fe³⁺ precipitation occurred between pH 3 and 4, although both Zn²⁺ and Fe³⁺ were present in the same solution during the entire range of pH titration. High-resolution transmission electron microscopy shows that the coprecipitates are 2 to 6 nm sized single crystalline particles but aggregated to 50 to 400 nm sized clusters. Analytical electron microscopy indicated that the 5% atomic Zn with respect to Fe was homogeneously distributed. No segregated phases were found in the clusters or at single crystal edges, which is consistent with published extended X-ray absorption fine structure (EXAFS) results at similar Zn/(Zn + Fe) ratios. Hence, occlusion and surface precipitation may be excluded as possible coprecipitation mechanisms. The bulk solution Zn²⁺ sorption edge was fitted to both solid solution and generalized diffuse layer surface complexation models. However, a solid solution model is inconsistent with published EXAFS results that show tetrahedral polydentate Zn²⁺ complexes sharing apices with Fe³⁺octahedra.     

Shock-induced amorphous textures in plagioclase,Manicouagan, Quebec,Canada

The textural relationships and structural states of optically isotropic labradorite from the Manicouagan, Quebec, impact structure have been examined by light (optical) and transmission electron (TEM) microscopy. Two distinct diaplectic glasses have been recognized based on their contrasting morphology, timing and the inferred modes of formation. The earliest isotropic bands and grain-scale isotropism (maskelynite) optically exhibit a gradational,in situ transformation from crystalline plagioclase with preservation of relict textures (twins, grain boundaries). The same transformation from crystalline to amorphous structure is observed in TEM to occur heterogeneously at scales on the order of the unit cell. The progressive transformation of optical properties reflects an increase in the volume fraction and eventual coalescence of these amorphous units. This maskelynite-type diaplectic glass is interpreted to form in the solid-state directly from crystalline material during the compressional phase of the shock wave. The other isotropic material occurs in spatially discrete tensiongashes and planar deformation features (PDFs) that overprint the maskelynite-type glass. This second type of diaplectic glass (PDF-type) is developed homogeneously within a given glass band and exhibits sharp crystal-glass boundaries, in contrast to the gradational boundaries of the maskelynite-type glass. PDF-type glass is interpreted to form by melting in tensional release zones during passage of the rarefaction wave. These observations emphasize the ability of naturally shocked rocks to preserve subtle evidence of variations in the shock process from highly transient events.     

Correlation between petrography,NAA, and ICP analyses: Application to early bronze Egyptian pottery from Canaan

Under favorable circumstances petrographic studies supported by chemical analysis using inductively coupled plasma (ICP) suffice to establish the provenience of pottery. A case in point is Egyptian-style pottery of Early Bronze Age found in Canaan. The pottery was divided into three groups according to four criteria determined by thin section analysis supplemented by X-ray diffraction: sorting and volume of silt-sized quartz, heavy minerals, the amount of carbonates in the matrix, and the firing temperature. Chemical analyses confirmed the classification. The source materials inferred for the three groups are Nile muds, Egyptian marly sediments, and local loess. Although the chemical analyses obtained by ICP and neutron activation analysis (NAA) were compatible, the existing database for NAA cannot be used indiscriminately. However, for provenience studies based on mineralogical and petrographic data, knowledge of the geology of the potential source areas can replace an extensive database.     

The thermal evolution of Corsica as recorded by zircon fission-tracks

New zircon fission-track (ZFT) ages from Corsica record multiple thermal events that can be tied to the structural evolution of the western Mediterranean region. The Corsican zircons have a wide scatter of ZFT grain ages (243–14 Ma), which together define several age domains. Western Corsica consists largely of stable Hercynian basement characterized by ZFT ages in the range 161–114 Ma. We interpret these ages (Late Jurassic–Early Cretaceous) as the product of a long-lived Tethyan thermal event related to continental rifting and subsequent drifting during the separation of the European and African plates and the formation of the Liguro–Piemontese ocean basin. In contrast to Hercynian Corsica, Alpine Corsica (northeast Corsica) experienced widespread deformation and metamorphism in Late Cretaceous(?)–Tertiary time. Dated samples from Alpine Corsica range in age from 112 to 19 Ma and all are reset or partially reset by one or more Alpine thermal events. The youngest ZFT grain ages are from the northernmost Alpine Corsica and define an age population at  24 Ma that indicates cooling after Tertiary thermal events associated with the Alpine metamorphism and the opening of the Liguro–Provençal basin. A less well-defined ZFT age population at  72 Ma is present in both Alpine Corsica and Hercynian basement rocks. The thermal history of these rocks is not clear. One interpretation is that the ZFT population at  72 Ma reflects resetting during a Late Cretaceous event broadly synchronous with the early Alpine metamorphism. Another interpretation is that this peak is related to variable fission-track annealing and partial resetting during the Tertiary Alpine metamorphic event across central to north-eastern Corsica. This partial age resetting supports the presence of a fossil ZFT partial annealing zone and limits the peak temperature in this area below 300 °C, for both the affected pre-Alpine and Alpine units.     

Geochemistry and petrogenesis of the Proterozoic dykes in Tamil nadu, southern India: another example of the Archaean lithospheric mantle source

Approximately 1650-Ma-old NW/SE and NE/SW-trending dolerite dykes in the Tiruvannamalai (TNM) area and approximately 1800-Ma-old NW/SE-trending dolerite dykes in the Dharmapuri (DP) area constitute major Proterozoic dyke swarms in the high-grade granulite region of Tamil nadu, southern India. The NW- and NE-trending TNM dykes are compositionally very similar and can be regarded as having been formed during a single magmatic episode. The DP dykes may relate to an earlier similar magmatic episode. The dolerites are Fe-rich tholeiites and most of the elemental variations can be explained in terms of fractional crystallisation. Clinopyroxene and olivine are the inferred ferromagnesian fractionation phases followed by plagioclase during the late fractionation stages. All the studied dykes have, similar to many continental flood basalts (CFB), large-ion lithophile element (LILE) and light rare-earth element (LREE) enrichment and Nb and Ta depletion. The incompatible element abundance patterns are comparable to the patterns of many other Proterozoic dykes in India and Antarctica, to the late Archaean (～2.72 Ga) Dominion volcanics in South Africa and to the early Proterozoic (～2.0 Ga) Scourie dykes of Scotland. The geochemical characteristics of the TNM and DP dykes cannot be explained by crustal contamination alone. Instead, they are consistent with derivation from an enriched lithospheric mantle source which appears to have been developed much earlier than the dyke intrusions during a major crustal building event in the Archaean. The dyke magmas may have been formed by dehydration melting induced by decompression and lithospheric attenuation or plume impingement at the base of the lithosphere. These magmas, compared with CFB, appear to be the minor partial melts from plume heads of smaller diameter and of shallow origin (650 km). Therefore, the Proterozoic thermal events could induce crustal attenuation and dyke intrusions in contrast to the extensive CFB volcanism and continental rifting generally associated with the Phanerozoic plumes of larger head diameter (>1000 km) and of deeper origin (at crust mantle boundary).     

The chemistry of lava-seawater interactions II: the elemental signature

The flow of lava into the ocean at the shoreline of Kilauea Volcano during the ongoing Pu’u O’o eruption has allowed a detailed study of the geochemical interaction between lava and seawater. This paper focuses on the chemistry of the major and minor elements in the fluids that resulted from this interaction. The elemental enrichments in these fluids are dominated by three processes: (1) evaporation of water from seawater, which creates solutions enriched in the major elements found in seawater, (2) congruent dissolution of the basalt glass matrix, which is limited by the solubility of some of the elements in seawater, and (3) removal of volatile phases from the lava on contact with seawater.Using a simple model of volatile emanation (using published emanation coefficients) and congruent dissolution, we are able to explain the concentrations observed for the majority of elements in precipitation from the steam plume at the shoreline lava entry and in water allowed to interact with molten lava in controlled experiments. Fe, Al, Ti, and some of the rare earth elements (REEs) in precipitation samples from the steam plume at the lava entry were > 10,000-times enriched over their ambient seawater concentrations, suggesting that these elements may be useful for identifying submarine eruptions. The flux of elements from the Kilauea ocean lava entry is greater than that from a typical midocean ridge hydrothermal vent field for Al, Cd, Co, and the REEs, whereas the opposite is true for the remainder of the elements studied.     

Basement-controlled faulting of Paleozoic strata in southern Ontario, Canada: new evidence from geophysical lineament mapping

Basement fault reactivation is now recognized as an important control on sedimentation and fault propagation in intracratonic basins. In southern Ontario, the basement consists of complexly structured mid-Proterozoic (ca. 1.2 Ga) crystalline rocks and metasedimentary rocks that are overlain by up to 1500 m of Paleozoic sedimentary strata. Reactivation of basement structures is suspected to control the location of Paleozoic fault and fracture systems, but evaluation has been hindered by a limited understanding of the regional structural characteristics of the buried basement. New aeromagnetic- and gravimetric-lineament mapping presented in this paper better resolves the location of basement discontinuities and provides further evidence for basement controls on the distribution of Paleozoic fault and fracture systems. Lineament mapping was facilitated by reprocessing and digital image enhancement (micro-levelling, regional residual separation, derivative filtering) of existing regional gravity and aeromagnetic datasets. Reprocessed images identify new details of the structural fabric of the basement below southern Ontario and delineate several previously unrecognized aeromagnetic and gravity lineaments and linear zones. Linear zones parallel the projected trends of mid-Proterozoic terrane boundaries identified by field mapping on the exposed shield to the north of the study area, and are interpreted as zones of shearing and basement faulting. Mapped aeromagnetic and gravity lineaments show similar trends to Paleozoic faults and fracture networks and broad zones of seismicity in southern Ontario. These new data support an ‘inheritance model’ for Paleozoic faulting, involving repeated reactivation and upward propagation of basement faults and fractures into overlying cover strata.     

Radiocarbon Ages and Environments of Deposition of the Wono and Trego Hot Springs Tephra Layers in the Pyramid Lake Subbasin, Nevada

Uncalibrated radiocarbon data from core PLC92B taken from Wizards Cove in the Pyramid Lake subbasin indicate that the Trego Hot Springs and Wono tephra layers were deposited 23,200 ± 300 and 27,300 ± 300¹⁴C yr B.P. (uncorrected for reservoir effect). Sedimentological data from sites in the Pyramid Lake and Smoke Creek–Black Rock Desert subbasins indicate that the Trego Hot Springs tephra layer was deposited during a relatively dry period when Pyramid Lake was at or below its spill point (1177 m) to the Winnemucca Lake subbasin. The Wono tephra layer was deposited when lake depth was controlled by spill across Emerson Pass sill (1207 m) to the Smoke Creek–Black Rock Desert subbasin.¹⁸O data from core PLC92B also support the concept that the Trego Hot Springs tephra fell into a relatively shallow Pyramid Lake and that the Wono tephra fell into a deeper spilling lake.