Search Results (5)

The stibnite mineralization at Rizana (Kilkis ore district; Serbo-Macedonian metallogenic province; northern Greece) occurs along a NE–SW-trending brittle shear-zone, which transects a two-mica and an augen-gneiss of the Vertiskos Unit. Barren Triassic A-type granites and satellite pegmatites and aplites, as well as Oligocene-Miocene plutonic, subvolcanic and volcanic rocks that are variably hydrothermally altered and mineralized, outcrop in the broader region. The mineralization appears as veins, discordant lodes and disseminations. Veins and discordant lodes exhibit massive and brecciated textures. Historic underground mining (1930s–1950s) produced 9000 t of stibnite ore, grading 40% Sb on average. The main ore mineral assemblage includes stibnite + berthierite + sphalerite + pyrite + chalcopyrite + native antimony and traces of wolframite, galena, tetrahedrite, marcasite, pyrrhotite, arsenopyrite, realgar, native arsenic and native gold. Quartz, minor barite and ankerite are the gangue minerals. Sericitization and silicification developed along the shear-zone, forming hydrothermal halos of moderate intensity in the two-mica gneiss. Locally, valentinite, goethite and claudetite are present due to the supergene oxidation of the stibnite mineralization. Bulk ore geochemistry shows enrichments in specific elements including As, Au, Cd, Se, Tl and W. Fluid inclusion microthermometry showed that the mineralization was formed under a limited range of temperatures and salinities. The fluids had low to slightly moderate salinities (6.6–8.1 wt% equiv. NaCl) with low homogenization temperatures (217–254 °C, with a maximum at 220 °C). Full article

The Gerakario Cu-Au porphyry deposit in the Kilkis ore district, northern Greece, contains epithermal quartz-stibnite veins on the eastern side of the deposit, which crosscut a two-mica gneiss. Metallic mineralization in these veins consists of stibnite + berthierite + native antimony + pyrite + arsenopyrite, and minor marcasite, pyrrhotite, chalcopyrite, löllingite, and native gold. Bulk geochemical analyses of the ore reveal an enrichment in critical and rare metals, including Ag, Au, Bi, Ce, Co, Ga, La, and Sb. Analysis of stibnite with LA-ICP-MS showed an enrichment in base metals (As, Cu, Pb), as well as weak to moderate contents of critical and rare metals (Ag, Bi, Ce, La, Re, Sm, Th, Ti, Tl). A statistical analysis of the trace elements show a positive correlation for the elemental pairs Ce-La, Ce-Sb, and La-Sb, and a negative correlation for the pair Bi-Sb. Fluid inclusions in the A-type veins of the porphyry-style mineralization show the presence of fluid boiling, resulting in a highly saline aqueous fluid phase (35.7 to 45.6 wt.% NaCl equiv.) and a moderately saline gas phase (14 to 22 wt.% NaCl equiv.) in the system H₂O-NaCl-KCl at temperatures varying between 380° and 460 °C and pressures from 100 to 580 bar. Mixing of the moderate saline fluid with meteoric water produced less saline fluids (8 to 10 wt.% NaCl equiv.), which are associated with the epithermal quartz-stibnite vein mineralization. This process took place under hydrostatic pressures ranging from 65 to 116 bar at a depth between 600 and 1000 m, and at temperatures mainly from 280° to 320 °C. Full article

The Vathi porphyry Cu-Au±Mo deposit is located in the Kilkis ore district, northern Greece. Hydrothermally altered and mineralized samples of latite and quartz monzonite are enriched with numerous rare and critical metals. The present study focuses on the bulk geochemistry and the mineral chemistry of pyrite, chalcopyrite, magnetite, and titanite. Pyrite and chalcopyrite are the most abundant ore minerals at Vathi and are related to potassic, propylitic, and sericitic hydrothermal alterations (A- and D-veins), as well as to the late-stage epithermal overprint (E-veins). Magnetite and titanite are found mainly in M-type veins and as disseminations in the potassic-calcic alteration of quartz monzonite. Disseminated magnetite is also present in the potassic alteration in latite, which is overprinted by sericitic alteration. Scanning electron microscopy and laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses of pyrite and chalcopyrite reveal the presence of pyrrhotite, galena, and Bi-telluride inclusions in pyrite and enrichments of Ag, Co, Sb, Se, and Ti. Chalcopyrite hosts bornite, sphalerite, galena, and Bi-sulfosalt inclusions and is enriched with Ag, In, and Ti. Inclusions of wittichenite, tetradymite, and cuprobismutite reflect enrichments of Te and Bi in the mineralizing fluids. Native gold is related to A- and D-type veins and is found as nano-inclusions in pyrite. Titanite inclusions characterize magnetite, whereas titanite is a major host of Ce, Gd, La, Nd, Sm, Th, and W. Full article

The Vathi porphyry Cu-Au ± Mo mineralization is located in the Serbo-Macedonian metallogenic province of the Western Tethyan Metallogenic Belt. It is mainly hosted by a latite and is genetically associated with a quartz monzonite intrusion, which intruded the basement rocks of the Vertiskos Unit and the latite, 18 to 17 Ma ago. A phreatic breccia crosscuts the latite. The quartz monzonite was affected by potassic alteration, whereas the latite was subjected to local propylitic alteration. Both styles of alteration were subsequently overprinted by intense sericitic alteration. M-type and A-type veins are spatially associated with potassic alteration, whereas D-type veins are related to the sericitic alteration. Three ore assemblages are associated with the porphyry stage: (1) pyrite + chalcopyrite + bornite + molybdenite + magnetite associated with potassic alteration; (2) pyrite + chalcopyrite related to propylitic alteration; and (3) pyrite + chalcopyrite + native gold ± tetradymite associated with sericitic alteration. A fourth assemblage consisting of sphalerite + galena + arsenopyrite + pyrrhotite + pyrite ± stibnite ± tennantite is related to an epithermal overprint. Fluid inclusion data indicate that the A-type veins and related porphyry-style mineralization formed at 390–540 °C and pressures of up to 646 bars (<2.6 km depth) from boiling hydrothermal fluids. A later condensation of vapor-rich inclusions resulted in a moderately saline fluid (8.4–11.2 wt % NaCl equiv) at temperatures between 311 and 392 °C, which were related to sericitic alteration, D-type veins, and associated metallic mineralization. Subsequent dilution of the moderately saline fluid at lower temperatures (205–259 °C) produced a less saline (1.4–2.9 wt % NaCl equiv.) fluid, which is likely associated with the late epithermal overprint. Full article

The European Union (EU) is highly dependent on critical and rare metals which are very important for a sustainable development. However, European industry is not able to cover its demands from native sources and it imports commodities from third countries. Greece is one of the EU countries with the most potential for supplying these strategic metallic raw materials in the future, since it hosts a large number of ore deposits. The epithermal- and porphyry-type deposits and the reduced intrusion related systems of the Serbomacedonian and the Rhodope metallogenic provinces in Northeastern Greece are promising targets for a future exploitation and exploration in Sb, Te, Mo, Re, Ga, In, REE and PGE. Greece is the leading producer of Ni and Al in the EU from laterites and bauxites of central and northern Greece. These deposits also contain significant amounts of Co or REE which should be considered in the future plans of the processing industries. REE are found in high contents at the placer deposits between Chalkidiki and Kavala (North Greece) and elevated PGE concentrations are associated with the chromitites of northwestern Greece. Therefore, the mineral wealth of Greece can contribute significantly to a sustainable and a competitive economy of Europe. Full article