Late Hercynian–Mesozoic thinning in the Alboran domain: metamorphic data from the northern Rif, Morocco

In the Alboran domain, two crustal-thickening late-orogenic extension cycles are superposed. The importance of the late Alpine thinning of the Alpujarride-Sebtide crustal section on top of the Beni Bousera peridotites is discussed here in metamorphic petrological terms. The Alpine metamorphism operated first under a HP–LT gradient, and reached the eclogite facies in the Permian–Triassic phyllites, before retrogression under a high geothermal gradient. A contrasting, higher temperature metamorphism characterizes the pre-Permian section, reaching the HP-granulite facies at the bottom of the crustal section. By reference to the western European setting, the granulites relate to the Hercynian orogeny, as supported by the isotopic ages of the enclosed, armoured monazite crystals. Thus, thinning of an overthickened crust might have occurred there during the late Hercynian extension and Tethyan opening, before being reactivated during the late Oligocene.     

Interstitial water chemistry of villefranche bay sediments: Trace metal diagenesis

Pore water aliquots were taken with an in situ close interval sampler: the “Peeper”.We report here the pore water concentration profiles of TCO₂, SO₄, TH₂S, Ca and the trace metals Mn, Cu, Pb, Cd and Cr from sediments of a relatively polluted area, the Villefranche Bay, on the French Riviera (close to Nice).We investigated the major ion concentrations in order to establish geochemical mass balances of organic matter oxidation. ΔTCO₂/ΔSO₄ was <−2.0, reflecting the precipitation of calcite as confirmed by the calcium profile. Reduction of sulfate led to increasing sulfide concentrations with depth.Trace metal interstitial water concentrations decreased from 63 to 5 nM, 18 to 4 nM and 6.6 to less than 2 nM for Cu, Pb and Cr, respectively. Cd showed a different pattern with top and deep values of 0.7 nM and a minimum of 0.27 nM.Thermodynamic calculations were performed which suggest the potential formation of mineral phases such as sulfides.     

Concentration du chrome dans deux profils de l'ocean pacifique

Determination of total chromium on two profiles and chromium III on four samples of equatorial Pacific Ocean water have been carried out using coprecipitation of chromium from sea water with hydrous iron oxides, followed by ion-exchange separation and isotope dilution mass spectrometry. Results for two Pacific profiles show increasing total chromium concentration from surface to 250 m. The Cr concentration appears to be different below 1,000 m, with nearly homogeneous concentrations for the first profile and regularly increasing Cr concentrations from 0.330 to 0.550 μg/l at 3,900 m for the second one. Results for Cr(III) show that trivalent species are dominant in these samples.     

Post‐Variscan exhumation of the Central Anti‐Atlas (Morocco) constrained by zircon and apatite fission‐track thermochronology

The origin of the Anti‐Atlas relief is one of the currently debated issues of Moroccan geology. To constrain the post‐Variscan evolution of the Central Anti‐Atlas, we collected nine samples from the Precambrian basement of the Bou Azzer‐El Graara inlier for zircon and apatite fission‐track thermochronology. Zircon ages cluster between 340 ± 20 and 306 ± 20 Ma, whereas apatite ages range from 171 ± 7 Ma to 133 ± 5 Ma. Zircon ages reflect the thermal effect of the Variscan orogeny (tectonic thickening of the ca. 7 km‐thick Paleozoic series), likely enhanced by fluid advection. Apatite ages record a complex Mesozoic–Cenozoic exhumation history. Track length modelling yields evidence that, (i) the Precambrian basement was still buried at ca. 5 km depth by Permian times, (ii) the Central Anti‐Atlas was subjected to (erosional) exhumation during the Triassic‐Early Cretaceous, then buried beneath ca. 1.5 km‐thick Cretaceous‐Paleogene deposits, (iii) final exhumation took place during the Neogene, contemporaneously with that of the High Atlas.     

The Ribeira fluorite district,southern Brazil

The origin and evolution of different ore deposits grouped in the same district are often complex and may involve inheritance from crustal or mantle geochemical anomalies, remobilization of former ore deposits and a polyphase hydrothermal history. Localized in a Proterozoic basement in the Parana state, the Ribeira fluorite district is such an example composed of three deposit types with distinct geological and geochemical characters. Emplaced at different periods from the late Proterozoic to the Cretaceous, they are roughly aligned along a belt nearly 10 km in width and 50 km in length, the southern boundary of which is a transcurrent fault. Two main ore facies are present: (1) microcrystalline ore (< 0.1 mm grains) and (2) macrocrystalline ore (with a grain size of several millimetres). The former results from the replacement of metalimestones or internal karstic sediments and the latter from microcrystalline ore dissolution and pore precipitation or recrystallization. At least two different groups of source rocks can be proposed for the trapped REE in CaF₂: (1) fluorite samples associated with the Mato Preto carbonatitic rocks display a slightly negative ɛNd compatible with a mantle source and a REE pattern with the higher ΣREE and La/Yb ratio in the district; (2) other fluorites have a strongly negative ɛNd (− 14 to − 20) which indicates a crustal source. That fluorine and REE have the same source is possible in strata-bound and fracture-filling deposits, but is doubtful at Mato Preto, the only economic fluorite deposit associated with carbonatite rocks in Brazil. This occurrence within a Precambrian fluorite belt suggests that remobilization of a former strata-bound deposit was a more significant metallogenic process than magmatic differentiation. Editorial handling: DR     

Comportement géochimique des éléments métalliques en milieu réducteur et diagrammes (log S,pH)

Résumé L'existence de relations entre les teneurs en carbonates et en sulfures dans les eaux des bassins réducteurs, ainsi que l'irreversibilité de la réaction sulfate-sulfure, conduisent à proposer le remplacement des diagrammes Eh. pH, par les diagrammes log S, pH (S désignant la concentration totale de S (-II)). Nous donnons ici le principe de construction, des exemples de diagrammes et quelques applications.

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The existence of relations between the amounts of carbonates and the sulfides in the water of anoxic basins and the irreversibility of the reaction sulphate-sulfide lead us to propose the substitution of diagrams Eh, pH by diagrams log S, pH (S being the total concentration of S (-II)). The principle of how diagrams should be drawn is outlined and some examples and applications are given.

     

Une méthode globale d'estimation des températures des réservoirs alimentant les sources thermales. Exemple du Massif Central Français

A chemical model based on the equilibrium of water with quartz, albite, adularia, calcite, kaolinite or illite, and chlorite can explain the chemical composition of the main groups of hot springs in Massif Central. Temperature is the principal variable for determining this composition. Model temperatures generally agree with those given by classical cation geothermometers (t ? 135–150° C for Vichy. La Bourboule. Evaux and Châteauneuf; t ? 175–180° C for Chaudes Aigues and Saint Nectaire). The model fails to represent the composition of Mont Dore waters: the high temperatures given by classical geothermometers are considered doubtful.     

Chimie du manganèse à l'interface eau sédiment

A manganese cycle at the oxidizing-reducing boundary is described as a concentration mechanism. The chemical properties of Mn can explain this cycle. A steady state model is used for quantitative estimation of the concentration efficiency.