This mineralogical and fluid inclusion study was conducted on an Au-bearing quartz–sulfide vein encountered in the deep parts of the Bytíz deposit in the Příbram uranium and base-metal district, Bohemian Massif, Czech Republic. The samples were taken where the Au-bearing vein is crosscut by the common base-metal Zn-Pb ore vein Bt23C. The early mineralization of the Au-bearing vein is composed mainly of quartz (Q-1 to Q-3), illite–muscovite, Fe-Mg chlorite, arsenopyrite, and Au-Ag alloys, showing a wide range of compositions (4–69 at. % Ag) and a decrease in Au/(Au + Ag) ratios during vein evolution. Younger hydrothermal processes led to the crystallization of nests and veinlets composed of late quartz (Q-4), carbonates (siderite, dolomite–ankerite and calcite), base-metal sulfides (galena, sphalerite, chalcopyrite, and tetrahedrite), a suite of Ag and Bi-tellurides, and acanthite. The input of Sb is manifested by the partial to complete replacement of some gold grains by aurostibite and an unnamed (Ag,Au)-Sb oxide with a composition close to AuSbO₃. The fluid inclusion study, combined with chlorite thermometry and arsenopyrite thermometry, showed that the early mineralization crystallized from progressively cooled (from 300 to 400 °C down to ca. 180 °C), diluted (1.2–7.0 wt. % NaCl eq.) aqueous solutions. The late portion of the mineralization formed from aqueous fluids with highly variable salinity (0.2–23.4 wt. % NaCl eq.) and homogenization temperatures decreasing from ca. 250 °C to < 50 °C, which compare well with the base-metal mineralization of the vein Bt23C and other base-metal veins of the Příbram ore area. Our study illustrates the nature and intensity of the processes of the reworking of the early gold mineralization mediated by the younger Ag,Sb-rich base-metal fluids, giving rise to Příbram’s typical late-Variscan vein Zn-Pb mineralization.

The paragenesis and composition of bavenite–bohseite were investigated in fifteen granitic pegmatites from the Bohemian Massif, Czech Republic. Three types distinct in their relation to primary Be precursors, mineral assemblages, morphology and origin were recognised: (1) primary hydrothermal bavenite–bohseite crystallised in miarolitic pockets from residual pegmatite fluids; and secondary bavenite–bohseite in two distinct types: (2) a proximal type restricted spatially to pseudomorphs after a primary Be mineral (beryl > phenakite, helvine–danalite); and (3) a distal type on brittle fractures and fissures of host pegmatite. The mineral assemblages are highly variable: (1) axinite-(Mn), smectite, calcite and pyrite; (2) bertrandite, milarite, secondary beryl, bazzite, K-feldspar, muscovite–illite, scolecite, gismondine-Ca, analcime, chlorite; and (3) muscovite, albite, quartz, epidote, pumpellyite-(Mg), pumpellyite-(Fe³⁺), titanite and chlorite. Electron microprobe analyses showed, in addition to major constituents (Si, Ca and Al), minor concentrations (in apfu) of Na (≤0.24), Fe (≤0.10), Mn (≤0.10) and F (≤0.36). The type 1 hydrothermal miarolitic bavenite–bohseite is mostly Al-rich (2.00–0.67 apfu) relative to type 2 proximal bavenite–bohseite and bohseite after beryl, phenakite and helvine–danalite (1.56–0.46, 0.70–0.05, 1.02–0.35 apfu, respectively); and type 3 distal bavenite–bohseite typically after beryl (1.63–0.09 apfu). Raman spectroscopy revealed that the distance between the OH^–vibrational modes decreases with increasing bohseite component. The Al content of secondary type 2 proximal bavenite–bohseite is controlled by the composition of the Be precursor whereas type 3 distal bavenite–bohseite with beryl as the Be precursor is more variable and the composition is governed mainly by the composition of fluids. Calcium, a crucial component for bavenite–bohseite origins, was derived from residual pegmatite fluids (Vlastějovice, Vepice IV or Třebíč Plutons) or external sources (e.g. Drahonín IV, Věžná I or Maršíkov). Primary type 1 hydrothermal bavenite–bohseite from miarolitic pockets might have crystallised atT≈ 300–400°C andP≈ 200 MPa, whereas the secondary type 2 and 3 bavenite–bohseite formed atT≈ 300–100°C andP≈ 200–20 MPa.

The aim of this study was to characterize historical slags which originated during silver production from the Jihlava ore district, Czech Republic. The area was among the head producers of silver within the Lands of the Czech Crown in 13th–14th centuries. The mined ores had complex composition, being formed mostly by pyrite, sphalerite, galena, chalcopyrite, and accessory silver-rich minerals such as silver-bearing tetrahedrite (freibergite) or pyrargyrite, with gangue represented by quartz and Mn-rich carbonates or baryte. Large volumes of slags with contrasting composition were generated during the Pb-Ag production. Altogether, two main types of slags were identified in the district. The first type is characterized by high BaO contents (up to 34.5 wt.%) and dominancy of glass, minor quartz, and accessory amounts of Ba-rich feldspar (up to 93 mol.% of Cls), metal-rich inclusions, Ba-Pb sulphates and only rare pyroxene, wollastonite and melilite. The composition of the second group belongs to fayalitic slags containing glass, Fe-rich olivine, accessory pyroxene, feldspar, quartz, and inclusions of various metallic phases. Fluxes were derived from gangue (quartz, carbonates, baryte) or local host rocks for both types of slag. The calculated viscosity indexes reflect (with minor exceptions) medium-to-high effectivity of metal separation. Smelting temperatures were estimated from a series of ternary plots; however, more reliable estimates for both types of slags were obtained only from experimental determination of melting temperature and calculations using bulk/glass compositions (~1100–1200 °C).

The Sn-W ore deposits in the Krupka surroundings are associated with greisens, which occur in the upper parts of Late Variscan granitoid intrusions. Fluid inclusions were studied in samples of quartz, cassiterite, apatite, fluorite, and topaz in greisenized granites, greisens, and hydrothermal veins with Sn-W mineralization. The greisenization process took place at temperatures 370–490 °C and pressures 155–371 bars, and associated fluids had predominantly low salinity and a low gas (CO₂, N₂ and CH₄) content. The post-greisenization stage was connected with the formation of (i) low-salinity (0–8 wt. % NaCl eq.) fluid inclusions with homogenization temperatures 35 wt. % NaCl eq.) fluid inclusions with homogenization temperatures 140–370 °C, often containing trapped crystals of quartz, topaz, and sulfides, or daughter crystals of salts and carbonates, which were identified by microthermometric measurements, electron microprobe analysis, and Raman spectroscopy. Analyses of fluid inclusion leachates have shown that Na and Ca chlorides predominate in fluids. According to hydrogen stable isotopes, the source of greisenizing and post-greisenizing fluids was not only magmatogenic but also meteoric water or fluids derived from sedimentary rocks.

Mineralogy and formation conditions were studied in a newly found vein wolframite mineralization, cutting migmatitized paragneisses in the exocontact of a small Carboniferous granite body in the Pohled quarry, Moldanubian Zone of the Bohemian Massif, Czech Republic. The early stage of the rich mineral assemblage (36 mineral species) involves wolframite, columbite-group minerals, molybdenite, and scheelite hosted by quartz–muscovite–chlorite gangue, which was followed by base-metal sulfides in a quartz gangue, whereas the last stage included calcite gangue with fluorite and minor sulfides. The mineral assemblage points to the mobility of usually hardly soluble elements, including W, Sn, Zr, Nb, Th, Ti, Sc, Y, and REEs. A fluid inclusion study indicates a significant decrease in homogenization temperatures from 350–370 °C to less than 100 °C during vein formation. Fluids were aqueous, with a low salinity (0–12 wt. % NaCl eq.) and traces of CO₂, N₂, CH₄, H₂, and C₂H₆. The δ¹⁸O values of the fluids giving rise to quartz and scheelite are positive (min. 4‰–6‰ V-SMOW). The Eh and pH of the fluid also changed during evolution of the vein. Both wolframite and columbite-group minerals are anomalously enriched in Mg. We suggest that the origin of this distinct mineralization was related to the mixing of Mo,W-bearing granite-derived magmatic fluids with external basinal waters derived from contemporaneous freshwater (but episodically evaporated) piedmont basins. The basinal waters infiltrated into the subsurface along fractures formed in the extensional tectonic regime, and their circulation continued even after the ending of the activity of magmatic fluids. The studied wolframite mineralization represents the most complete record of the ‘hydrothermal’ history of a site adjacent to a cooling granite body in the study area. Moreover, there are broad similarities in the mineral assemblages, textures, and chemical compositions of individual minerals from other occurrences of wolframite mineralization around the Central Moldanubian Plutonic Complex, pointing to the genetic similarities of the Variscan wolframite-bearing veins in this area.

The Václav vein (Březové Hory deposit, Příbram ore area, Czech Republic) is a base–metal vein containing minor Cu-Zn-Pb-Ag-Sb sulfidic mineralization in a usually hematitized gangue. A detailed mineralogical study using an electron microprobe revealed a complicated multistage evolution of the vein. Early siderite and Fe-rich dolomite were strongly replaced by assemblages of hematite+rhodochrosite and hematite+kutnohorite/Mn-rich dolomite, respectively. In addition, siderite also experienced strong silicification. These changes were associated with the dissolution of associated sulfides (sphalerite, galena). The following portion of the vein contains low-Mn dolomite and calcite gangue with Zn-rich chlorite, wittichenite, tetrahedrite-group minerals, chalcopyrite, bornite, and djurleite, again showing common replacement textures in case of sulfides. The latest stage was characterized by the input of Ag and Hg, giving rise to Ag-Cu sulfides, native silver (partly Hg-rich), balkanite, and (meta)cinnabar. We explain the formation of hematite-bearing oxidized assemblages at the expense of pre-existing “normal” Příbram mineralization due to repeated episodic infiltration of oxygenated surface waters during the vein evolution. Episodic mixing of ore fluids with surface waters was suggested from previous stable isotope and fluid inclusion studies in the Příbram ore area. Our mineralogical study thus strengthens this genetic scenario, illustrates the dynamics of fluid movement during the evolution of a distinct ore vein structure, and shows that the low content of ore minerals cannot be necessarily a primary feature of a vein.