Les tholeiites a affinité alcaline du secteur ouest du Siroua (Anti-Atlas central, Maroc): temoins d'une distension au Néoproterozoïque

The Upper Proterozoic granitoids of the western part of the Siroua Massif (central Anti-Atlas, Morocco) are cut by doleritic dykes injected along submeridian and equatorial directions. These dykes were emplaced before deposition of late Neoproterozoic formations (PIII). According to and incompatible element ratios, these dolerites constitue two discrete chemical groups unrelated to orientation and thickness. They are both enriched in large ion lithophile elements, Zr, Th and light rare earth elements, and correspond to continental tholeiites displaying an alkaline affinity. This alkaline affinity is also confirmed by clinopyroxene and amphibole chemistry. Emplacement of these doleritic dykes occurred under an extensional regime active in the Anti-Atlas range during the Upper Proterozoic.     

Application of the Ti-in-quartz thermobarometer to rutile-free systems. Reply to: a comment on: ‘TitaniQ under pressure: the effect of pressure and temperature on the solubility of Ti in quartz’ by Thomas et al.

The premise of the Wilson et al. comment is that the Ti-in-quartz solubility calibration (Thomas et al. in Contrib Mineral Petrol 160:743–759, 2010) is fundamentally flawed. They reach this conclusion because P–T estimates using the Ti-in-quartz calibration differ from their previous interpretations for crystallization conditions of the Bishop and Oruanui rhyolites. If correct, this assertion has far-reaching implications, so a careful assessment of the Wilson et al. reasoning is warranted. Application of the Ti-in-quartz calibration as a thermobarometer in rutile-free rocks requires an estimation of TiO₂ activity in the liquid ( (liquid–rutile); referenced to rutile saturation) and an independent constraint on either P or T to obtain the crystallization temperature or pressure, respectively. The foundation of Wilson et al.’s argument is that temperature estimates obtained from Fe–Ti oxide thermometry accurately reflect crystallization conditions of quartz in the two rhyolites discussed. We maintain that our experimental approach is sound, the thermodynamic basis of the Ti-in-quartz calibration is fundamentally correct, and our experimental results are robust and reproducible. We suggest that the reason Wilson et al. obtain implausible pressure estimates is because estimates for T and they used as input values for the Ti-in-quartz calibration are demonstrably too high. Numerous studies show that Fe–Ti oxide temperature estimates of some rhyolites are substantially higher than those predicted by well-constrained phase equilibria. In this reply, we show that when reasonable input values for T and (liquid–rutile) are used, pressure estimates obtained from the Ti-in-quartz calibration are well aligned with phase equilibria and essentially identical to melt inclusion volatile saturation pressures.     

New Chronological,Paleontological, and Geochemical Data on the Formation of Glacier-Dammed Lakes in the Kurai Depression (Southeastern Russian Altai) at the End of the Late Pleistocene

Doklady Earth Sciences - One of the debated problems in Pleistocene paleogeography of the Altai region is the extent and time of existence of the last glacier-dammed lakes. For the first time...     

Patterns of Nd and Sr isotopic ratios produced by magmatic and post-magmatic processes in the Shiant Isles Main Sill, Scotland

The Shiant Isles Main Sill of the British Tertiary Igneous Province is a classic example of a differentiated, alkaline basic sill. Four separate intrusions, each emplaced internally in rapid succession, form a 165-m-thick sill hosted by Lower Jurassic sedimentary rocks. Extensive Nd and Sr isotopic studies were conducted on samples from a vertical section through the sill where the relationships of samples to one another are well defined. The results illuminate patterns of modification of isotopic ratios and clarify the petrogenesis (magma sources, crustal contamination), magmatic processes (bulk mixing, interstitial liquid mixing), and post-magmatic alteration (hydrothermal effects on Sr and Nd). Overall, the whole-rock initial ⁸⁷Sr/⁸⁶Sr ratios range from ∼0.7037 to 0.7061 while initial ¹⁴³Nd/¹⁴⁴Nd ratios vary from ∼0.51243 to 0.51286 (ɛ_Nd∼−0.7 to +5.7) – values that contrast markedly with those of the country rock. Acid leaching (HCl) of the whole-rock samples that removes analcime indicates that most of the scatter in the ⁸⁷Sr/⁸⁶Sr is caused by the ubiquitous sub-solidus, aqueous alteration during which more-radiogenic Sr was introduced into the sill, especially along the margins, and also reveals magmatic isotopic ratios. In contrast, Nd was immobile during fluid interaction so that the sill ¹⁴³Nd/¹⁴⁴Nd ratios were not affected, even <1 m from the country-rock contact. Using leached rock values, ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios are inversely correlated from magmatic processes. Magmas with two distinct isotopic compositions were involved: a more primitive one with ¹⁴³Nd/¹⁴⁴Nd ∼0.51285 and ⁸⁷Sr/⁸⁶Sr ∼0.7035 that produced the first two intrusions and a more evolved one (with 0.51252 and 0.7048) that produced the third intrusion. Mixing of the two magmas was very limited, restricted to near contacts between units, and apparently occurred by interstitial melt migration. The more evolved crinanitic magma was probably produced from a batch of the more primitive picritic melt by a small degree of crustal contamination and crystal fractionation during a short crustal residence prior to ascent and emplacement. Received: 20 December 1999 / Accepted: 5 May 2000     

Yearly and seasonal variations of low albedo surfaces on Mars in the OMEGA/MEx dataset: Constraints on aerosols properties and dust deposits

The time variations of spectral properties of dark martian surface features are investigated using the OMEGA near-IR dataset. The analyzed period covers two Mars years, spanning from early 2004 to early 2008 (includes the 2007 global dust event). Radiative transfer modeling indicates that the apparent albedo variations of low to mid-latitude dark regions are consistent with those produced by the varying optical depth of atmospheric dust as measured simultaneously from the ground by the Mars Exploration Rovers. We observe only a few significant albedo changes that can be attributed to surface phenomena. They are small-scaled and located at the boundaries between bright and dark regions. We then investigate the variations of the mean particle size of aerosols using the evolution of the observed dark region spectra between 1 and 2.5 μm. Overall, we find that the observed changes in the spectral slope are consistent with a mean particle size of aerosols varying with time between 1 and 2 μm. Observations with different solar zenith angles make it possible to characterize the aerosol layer at different altitudes, revealing a decrease of the particle size of aerosols as altitude increases.     

An intercomparison of seawater filtration procedures

Filtration systems, used for the preparation of coastal seawater samples for trace analysis, have been intercompared to determine the extent of contamination arising during the filtration process. The results show that all the systems intercompared are able to provide uncontaminated filtrates for copper, nickel, cobalt and manganese and, with two exceptions, for cadmium and iron, at levels that would be encountered in uncontaminated coastal waters.     

SYN-SEDIMENTARY MARINE LITHIFICATION OF MIDDLE JURASSIC LIMESTONES IN THE PARIS BASIN

SUMMARY
Bored surfaces in Middle Jurassic limestones in northeastern France indicate syn-sedimentary lithification. The sedimentary structures and textures, and age relationships between the bored carbonates and the argillaceous sediments above them suggest that the lithification has occurred in both submarine and intertidal environments. The diagenetic fabrics which have resulted from this early marine lithification include three types of calcite druse, echinoderm overgrowths, and microcrystalline cements. Most of these cements are comparable with those forming today in inter- and subtidal environments of the Persian Gulf.
The localization of bored surfaces ("hard grounds") at the tops of regressive carbonate sequences is interpreted as being the result of slow carbonate sedimentation and lithification of the Jurassic sea-floor prior to the onset of argillaceous colder, or deeper-water sedimentation.     

Diffusion of tetravalent cations in zircon

Diffusion rates for the three tetravalent cations U, Th and Hf have been measured in synthetic zircon. Diffusant sources included oxide powders and ground pre-synthesized silicates. Rutherford backscattering spectrometry (RBS) was used to measure depth profiles. Over the temperature range 1400–1650 °C, the following Arrhenius relations were obtained (diffusion coefficients in m²sec⁻¹): log D _Th = (1.936 ± 0.9820) + (− 792 ± 34 kJ mol⁻¹ /2.303 RT) log D _U = (0.212 ± 2.440) + (− 726 ± 83 kJ mol⁻¹ /2.303 RT) log D _Hf = (3.206 ± 1.592) + (− 812 ± 54 kJ mol⁻¹ /2.303 RT) The data show a systematic increase in diffusivity with decreasing ionic radius (i.e., faster diffusion rates for Hf than for U or Th), a trend also observed in our earlier study of rare earth diffusion in zircon. Diffusive fractionation may be a factor in the Lu-Hf system given the much slower diffusion rates of tetravalent cations when compared with the trivalent rare earths. The very slow diffusion rates measured for these tetravalent cations suggest that they are essentially immobile under most geologic conditions, permitting the preservation of fine-scale chemical zoning and isotopic signatures of inherited cores. Received: 12 July 1996 / Accepted: 2 December 1996