Mineralogical and geochemical evidence for multi-stage origin of mineral veins hosted by teschenites at Tichá, Outer Western Carpathians,Czech Republic     

Zdeněk Dolníček  Kamil Kropáč  Pavel Uher  Martin Polách 《Chemie der Erde / Geochemistry》2010,70(3):267-282

Numerous mineral veins are hosted in a body of teschenite which is situated within the Lower Cretaceous flysch siliciclastics of the Silesian Unit at Tichá. Mineralogy, fluid inclusions, stable isotopes and trace elements have been studied in order to assess the origin of this mineralization. Three stages of vein cementation have been recognized, each of them being characterized by distinct mineral composition and genetic conditions. The first stage is composed of titanite, aegirine-augite to aegirine, annite, analcime and strontian apatite. These minerals originated from NaCl-rich, CaCl₂-poor magmatic brine (total fluid salinities range between 47 and 57 wt%), leaving after crystallization of host teschenite in low-pressure (<1 kbar) environment. Crystallization temperatures reached ～390–510 °C for early phases, titanite and aegirine-augite. The second stage is formed by calcite, chlorite, dolomite, siderite, strontianite, quartz, pyrite and sphalerite. The parent fluids were low-salinity (0.5–4.5 wt% NaCl eq.) aqueous solutions with low content of strong REE-complexing ligands, that were progressively cooled during mineral precipitation (up to ～190 °C at the beginning, ～90 °C at the end of crystallization). These fluids are interpreted to be predominantly of external origin, derived from surrounding sedimentary sequences during diagenetic dewatering of clay minerals. The highly positive δ¹⁸O and near-zero δ¹³C values indicate an interaction of fluids with sedimentary carbonates. The third stage is formed by a dense net of calcite veinlets, which probably originated during tectonic deformations connected with orogenetic movements during the Tertiary. The source of strontium for first stage mineralization was probably related to the special conditions of magmatic evolution of the host teschenite, whereas strontium for second stage minerals could have been remobilized during hydrothermal alteration from earlier teschenite-hosted mineral phases and/or limestone.  相似文献   

Geochemical characteristics of the high- and low-Ti basaltic rocks from the uplifted shoulder of the Ohře (Eger) Rift,Western Bohemia     

Jaromír Ulrych  Emil Jelínek  Zdeněk Řanda  Felicity E. Lloyd  Kadosa Balogh  Ernst Hegner  Jiří K. Novák 《Chemie der Erde / Geochemistry》2010,70(4):319-333

High-Ti melanephelinite (3.8–5.9 wt% TiO₂), medium-Ti (phono)tephrite (2.7–3.1 wt% TiO₂), and low-Ti olivine melanephelinite/basanite (1.9–2.3 wt.% TiO₂) are subordinate rock types in the central European Cenozoic Volcanic Province. A contrasting melanephelinite to (phono)tephrite series occurs in the Lou?ná–Oberwiesenthal Volcanic Centre (37–28 Ma) and also as satellite volcanic bodies (26–12 Ma) together with olivine melanephelinite/basanite (17–20 Ma) on the southwestern periphery of the Kru?né hory mountains (Erzgebirge). The volcanic rocks intrude the Variscan basement of the uplifted shoulder of the Oh?e/Eger Rift in the Kru?né hory mountains of the Bohemian Massif. Low Mg# (44–59) and Cr, Ni contents and enrichment of LILE, Zr, Hf, Nb, Ta, U, Th and LREE in the high-Ti melanephelinites contrast with the composition of primitive low-Ti olivine melanephelinites/basanites displaying high Mg# (63–74) and high contents of compatible elements. The high-Ti melanephelinites reveal a wide range in initial ⁸⁷Sr/⁸⁶Sr of ca. 0.7034–0.7038 and ε_Nd of 2.4–4.9. The low-Ti melanephelinites show an overlapping range of initial ⁸⁷Sr/⁸⁶Sr of ca. 0.7035–0.7036 and ε_Nd of 4.3–5.5. The large variation in initial ⁸⁷Sr/⁸⁶Sr ratios at similar ε_Nd values in those rock types is interpreted as evidence for melting of metasomatized lithospheric mantle sources comprising K-bearing phases with radiogenic Sr. Modification of the olivine-free alkali basaltic magmas by differentiation or crustal contamination could give rise to the medium-Ti (phono) tephrites. The initial isotope ratios of all samples are consistent with HIMU-mantle sources and contributions from lithospheric mantle. The olivine-free melanephelinitic rocks often contain alkali pyroxenite–ijolite xenoliths with initial ⁸⁷Sr/⁸⁶Sr ratios of ca. 0.7036 and ε_Nd of 3.0. We interpret these xenoliths as samples of an intra-crustal alkali complex derived from similar mantle sources as those for the basaltic volcanic rocks.  相似文献   

Formation of the Vysoká–Zlatno Cu–Au skarn–porphyry deposit, Slovakia     

Peter Koděra  Jaroslav Lexa  Anthony E. Fallick 《Mineralium Deposita》2010,45(8):817-843

The central zone of the Miocene Štiavnica stratovolcano hosts several occurrences of Cu–Au skarn–porphyry mineralisation, related to granodiorite/quartz–diorite porphyry dyke clusters and stocks. Vysoká–Zlatno is the largest deposit (13.4 Mt at 0.52% Cu), with mineralised Mg–Ca exo- and endoskarns, developed at the prevolcanic basement level. The alteration pattern includes an internal K- and Na–Ca silicate zone, surrounded by phyllic and argillic zones, laterally grading into a propylitic zone. Fluid inclusions in quartz veinlets in the internal zone contain mostly saline brines with 31–70 wt.% NaCl eq. and temperatures of liquid–vapour homogenization (Th) of 186–575°C, indicating fluid heterogenisation. Garnet contains inclusions of variable salinity with 1–31 wt.% NaCl eq. and Th of 320–360°C. Quartz–chalcopyrite veinlets host mostly low-salinity fluid inclusions with 0–3 wt.% NaCl eq. and Th of 323–364°C. Data from sphalerite from the margin of the system indicate mixing with dilute and cooler fluids. The isotopic composition of fluids in equilibrium with K-alteration and most skarn minerals (both prograde and retrograde) indicates predominantly a magmatic origin (δ¹⁸O_fluid 2.5–12.3‰) with a minor meteoric component. Corresponding low δD_fluid values are probably related to isotopic fractionation during exsolution of the fluid from crystallising magma in an open system. The data suggest the general pattern of a distant source of magmatic fluids that ascended above a zone of hydraulic fracturing below the temperature of ductile–brittle transition. The magma chamber at ∼5–6 km depth exsolved single-phase fluids, whose properties were controlled by changing PT conditions along their fluid paths. During early stages, ascending fluids display liquid–vapour immiscibility, followed by physical separation of both phases. Low-salinity liquid associated with ore veinlets probably represents a single-phase magmatic fluid/magmatic vapour which contracted into liquid upon its ascent.  相似文献