Search Results (7)

We present a data set of calcite twinning strain results (n = 209 samples; 9919 measured calcite twins) from the internal Alpine nappes northwestward across the Alps and Alpine foreland to the older extensional margin along the Atlantic coast in Ireland. Along the coast of Northern Ireland, Cretaceous chalks and Tertiary basalts are cross-cut by calcite veins and offset by calcite-filled normal and strike-slip faults. Both Irish sample suites (n = 16 with four U-Pb vein calcite ages between 70–42 Ma) record a sub-horizontal SW-NE shortening strain with vertical extension and no strain overprint. This sub-horizontal shortening is parallel to the margin of the opening of the Atlantic Ocean (~58 Ma), and this penetrative fabric is only observed ~100 km inboard of the margin to the southeast. The younger, collisional Alpine orogen (~40 Ma) imparted a stress–strain regime dominated by SE-NW sub-horizontal shortening ~1200 km northwest from the Alps preserved in Mesozoic limestones and calcite veins (n = 32) in France, Germany and Britain. This layer-parallel shortening strain (−3.4%, 5% negative expected values) is preserved across the foreland in the plane of Alpine thrust shortening (SE-NW) along with numerous outcrop-scale contractional structures (i.e., folds, thrust faults). Calcite veins were observed in the Alpine foreland in numerous orientations and include both a SE-NW layer-parallel shortening fabric (n = 11) and a sub-vertical NE-SW vein-parallel shortening fabric (n = 4). Alpine foreland strains are compared with twinning strains from the frontal Jura Mountains (n = 9; layer-parallel shortening), the Molasse basin (n = 26; layer-parallel and layer-normal shortening), Pre-Alp nappes (n = 39; layer-parallel and layer-normal shortening), Helvetic and Penninic nappes (Penninic klippe; n = 46; layer-parallel and layer-normal shortening plus four striated U-Pb calcite vein ages ~24 Ma) and calcsilicates from the internal Tauern window (n = 4; layer-normal shortening). We provide a chronology of the stress–strain history of the European plate from 58 Ma through the Alpine orogen. Full article

Silicocarbonate pegmatites from the southern Grenville Province have provided exceptionally large crystal specimens for more than a century. Their mineral parageneses include euhedral calc–silicate minerals such as amphibole, clinopyroxene, and scapolite within a calcite matrix. Crystals can reach a meter or more in long dimension. Minor and locally abundant phases reflect local bedrock compositions and include albite, apatite, perthitic microcline, phlogopite, zircon, tourmaline, titanite, danburite, uraninite, sulfides, and many other minerals. Across the Adirondack Region, individual exposures are of limited aerial extent (<10,000 m²), crosscut metasedimentary rocks, especially calc–silicate gneisses and marbles, are undeformed and are spatially and temporally associated with granitic pegmatites. Zircon U–Pb results include both Shawinigan (circa 1165 Ma) and Ottawan (circa 1050 Ma) intrusion ages, separated by the Carthage-Colton shear zone. Those of Shawinigan age (Lowlands) correspond with the timing of voluminous A-type granitic magmatism, whereas Ottawan ages (Highlands) are temporally related to orogenic collapse, voluminous leucogranite and granitic pegmatite intrusion, iron and garnet ore development, and pervasive localized hydrothermal alteration. Inherited zircon, where present, reflects the broad range of igneous and detrital ages of surrounding rocks. Carbon and oxygen isotopic ratios from calcite plot within a restricted field away from igneous carbonatite values to those of typical sedimentary carbonates and local marbles. Collectively, these exposures represent a continuum between vein-dyke and skarn occurrences involving the anatexis of metasedimentary country rocks. Those of Ottawan age can be tied to movement and fluid flow along structures accommodating orogenic collapse, particularly the Carthage-Colton shear zone. Full article

The paper provides details of local geology and mineralogy of the Tazheran Massif, which was the sampling site of perovskite used as an external standard in perovskite U-Pb dating by sensitive high-resolution ion microprobe (SHRIMP) and laser ablation inductively-coupled plasma (LA–ICP–MS) mass spectrometry. The Tazheran Massif is a complex of igneous (mafic dikes, syenite, nepheline syenite), metamorphic (marble), and metasomatic (skarn, calc–silicate veins) rocks. Metasomatites are thin and restricted to the complex interior being absent from the margins. Perovskite has been studied at four sites of metasomatic rocks of three different types: forsterite–spinel calc–silicate veins in brucite marble (1); skarn at contacts between nepheline syenite and brucite marble (2), and skarn-related forsterite–spinel (Fo-Spl) calc–silicate veins (3). Pervoskite from Fo-Spl calc–silicate veins (type 1) is almost free from impurities (<1 wt.% in total: 0.06%–0.4% REE₂O₃, 0.10%–0.22% Nb₂O₅, ≤0.1% ThO₂). The U contents are from 0.1 to 1.9 wt.% UO₂ and are relatively uniform in perovskites from the same vein but differ from vein to vein of this type. Perovskite from the contact skarn (type 2) contains 1.5 to 4.5 wt.% REE₂O₃ but is poor in other impurities. Perovskite grains from skarn-related Fo-Spl calc–silicate rocks (type 3) belong to two generations that differ in REE, Nb, Th, Fe, and Na concentrations. Early-generation perovskites occurs as compositionally homogeneous octahedral or cubic-octahedral crystals with contents of impurities higher than in other varieties (3.6 wt.% REE₂O₃, 1.6 wt.% Fe₂O₃, 1.3 wt.% Nb₂O₅, 0.7 wt.% ThO₂, 0.6 wt.% UO₂, and 0.6 wt.% Na₂O) but the lowest is at the respective site. Late-generation varieties show highly variable impurity concentrations of 1.5 to 22.7 wt.% REE₂O₃, 0.4 to 8.4 wt.% Nb₂O₅, and 0.8 to 4.5% ThO₂, while the perovskite component may be as low as 65%. In addition to the lueshite and loparite, components, they contain REEFeO₃ and Th_0.5TiO₃ endmembers which have no natural analogs. Full article

The Trikorfo area (Thassos Island, Rhodope massif, Northern Greece) represents a unique mineralogical locality with Mn-rich minerals including kyanite, andalusite, garnet and epidote. Their vivid colors and large crystal size make them good indicators of gem-quality materials, although crystals found up to now are too fractured to be considered as marketable gems. The dominant lithology is represented by a garnet–kyanite–biotite–hematite–plagioclase ± staurolite ± sillimanite paragneiss. Thermodynamic Perple_X modeling indicates conditions of ca. 630–710 °C and 7.8–10.4 kbars. Post-metamorphic metasomatic silicate and calc-silicate (Mn-rich)-minerals are found within (i) green-red horizons with a mineralogical zonation from diopside, hornblende, epidote and grossular, (ii) mica schists containing spessartine, kyanite, andalusite and piemontite, and (iii) weakly deformed quartz-feldspar coarse-grained veins with kyanite at the interface with the metamorphic gneiss. The transition towards brittle conditions is shown by Alpine-type tension gashes, including spessartine–epidote–clinochlore–hornblende-quartz veins, cross-cutting the metamorphic foliation. Kyanite is of particular interest because it is present in the metamorphic paragenesis and locally in metasomatic assemblages with a large variety of colors (zoned blue to green/yellow-transparent and orange). Element analyses and UV-near infrared spectroscopy analyses indicate that the variation in color is due to a combination of Ti⁴⁺–Fe²⁺, Fe³⁺ and Mn³⁺ substitutions with Al³⁺. Structural and mineralogical observations point to a two-stage evolution of the Trikorfo area, where post-metamorphic hydrothermal fluid circulation lead locally to metasomatic reactions from ductile to brittle conditions during Miocene exhumation of the high-grade host-rocks. The large variety of mineral compositions and assemblages points to a local control of the mineralogy and fO₂ conditions during metasomatic reactions and interactions between hydrothermal active fluids and surrounding rocks. Full article

Epithermally altered volcanic rocks in Greece host amethyst-bearing veins in association with various silicates, carbonates, oxides and sulfides. Host rocks are Oligocene to Pleistocene calc-alkaline to shoshonitic lavas and pyroclastics of intermediate to acidic composition. The veins are integral parts of high to intermediate sulfidation epithermal mineralized centers in northern Greece (e.g., Kassiteres–Sapes, Kirki, Kornofolia/Soufli, Lesvos Island) and on Milos Island. Colloform–crustiform banding with alternations of amethyst, chalcedony and/or carbonates is a common characteristic of the studied amethyst-bearing veins. Hydrothermal alteration around the quartz veins includes sericitic, K-feldspar (adularia), propylitic and zeolitic types. Precipitation of amethyst took place from near-neutral to alkaline fluids, as indicated by the presence of various amounts of gangue adularia, calcite, zeolites, chlorite and smectite. Fluid inclusion data suggest that the studied amethyst was formed by hydrothermal fluids with relatively low temperatures (~200–250 °C) and low to moderate salinity (1–8 wt % NaCl equiv). A fluid cooling gradually from the external to the inner parts of the veins, possibly with subsequent boiling in an open system, is considered for the amethysts of Silver Hill in Sapes and Kassiteres. Amethysts from Kornofolia, Megala Therma, Kalogries and Chondro Vouno were formed by mixing of moderately saline hydrothermal fluids with low-salinity fluids at relatively lower temperatures indicating the presence of dilution processes and probably boiling in an open system. Stable isotope data point to mixing between magmatic and marine (and/or meteoric) waters and are consistent with the oxidizing conditions required for amethyst formation. Full article

The Shah-Ali-Beiglou epithermal base metal-silver deposit is located in the Tarom-Hashjin metallogenic province (THMP) in northwestern Iran. This deposit is hosted by quartz monzonite dikes of Oligocene age and surrounded by andesite to trachyandesite volcanic and volcaniclastic rocks of Eocene age. The subvolcanic rocks in the study area vary in composition from quartz-monzonite to monzonite and have metaluminous, calc-alkaline to shoshonitic affinity. These rocks have I-type geochemical characteristic and are related to post-collisional tectonic setting. The mineralization occurs as NE-SW and E-W-trending brecciated veins controlled by strike-slip and normal faults, which are associated to the Late Oligocene compressional regime. The mineral paragenesis of the vein mineralization is subdivided into pre-ore stage, ore stage, post-ore stage, and supergene stage. Pre-ore stage is dominated by quartz, sericite, and subhedral to anhedral pyrite as disseminated form. Ore-stage is represented by quartz, sphalerite (from 0.1 mol % to 4 mol % FeS), galena, chalcopyrite, tetrahedrite-tennantite, minor seligmannite and enargite, as vein-veinlet, cement and clast breccias. Post-ore stage is defined by deposition of quartz and carbonate along with minor barite, and supergene stage is characterized by bornite, chalcocite, covellite, hematite, goethite, and jarosite. The ore mineralization is associated with the silicic alteration. The styles of alteration are silicic, carbonate, sericitic, chloritic, and propylitic. Fluid inclusions in sphalerite have a wide range of salinities between 0.35 wt % and 21.4 wt % NaCl equivalent and homogenization temperatures range from 123 to 320 °C. The isotopic values of sulfides vary from 2.8‰ to 6.7‰ suggesting a magmatic source for the sulfur. In the present study, based on geological setting, alteration style of the host and wall rocks, main textures, mineral assemblages, composition of ore minerals, and structural features, it is suggested that the mineralization in the Shah-Ali-Beiglou is similar to intermediate-sulfidation style of epithermal deposits. Full article

The Peräpohja belt comprises a greenschist to amphibolite facies; multiply-folded supracrustal sequence of quartzites; mafic volcanics; carbonate rocks; black shales; mica schists and greywackes deposited from ca. 2.44 Ga to 1.92 Ga; during protracted rifting of the Archaean basement. Metamorphism and multiple folding of the basin fill occurred during the Svecofennian orogeny (1.92–1.80 Ga). The Rompas Au–U mineralization is hosted within deformed and metamorphosed calcsilicate veins in mafic volcanics. Textural evidence suggests that deposition and periods of uraninite re-mobilization were followed by localized hydrocarbon-bearing fluid flow which produced pyrobitumen crusts around grains of uraninite. Gold precipitated during the latest hydrothermal event at around 1.75 Ga. In situ U–Pb dating of uraninite by laser ablation inductively coupled mass spectroscopy (LA-ICP-MS), and Re–Os dating of molybdenite, indicate that primary hydrothermal uranium mineralization forms two age clusters; about 2.03–2.01 and 1.95–1.94 Ga. Resetting of the U–Pb system and precipitation of new generations of uraninite are associated with major deformation and metamorphic stages of the Svecofennian orogeny at 1.91–1.89 Ga, 1.85 Ga, and 1.80 Ga. Gold deposition was synchronous with the emplacement of the 1.75–1.78 Ga late/post-orogenic granitoids. The gold-producing hydrothermal event is also recorded by Re–Os dating of molybdenite from the gold-bearing Mg-metasomatized metasedimentary and metavolcanic units at the Palokas prospect; a few kilometres from Rompas. Results of this study confirm that some domains in the structure of uraninite may preserve the original crystallization age, despite an overprinting amphibolite facies metamorphic and other hydrothermal events. The study supports the utility of in situ U–Pb dating of uraninite and the ability of Re–Os dating to assist in sorting out different hydrothermal events in areas with complex tectonic; magmatic and metamorphic histories. Full article