Search Results (11)

The Evevpenta gold–silver epithermal deposit, belonging to an adularia–sericite or low-sulfidation type, is in the northern part of the Kamchatka Peninsula within the Oligocene–Quaternary Central Kamchatka volcanic belt. Variously native gold, silver, and Au–Ag chalcogenides, including calaverite, petzite, hessite, acanthite, uytenbogaardtite-petrovskaite, and naumannite, constitute its Au–Ag mineralization. Extensive fluid inclusion studies, involving fluid inclusion petrography, Raman spectroscopy, and microthermometry, revealed that quartz from gold-bearing adularia–quartz veins crystallized from low-salinity fluids (T ice melting from −0.1 to −3.3 °C) at moderate to low temperatures (140 to 364 °C). The mineralizing fluids consisted of Na, K, and Mg sulfate and bicarbonate-bearing aqueous solutions and low-density CO₂. The gold-bearing mineral assemblages were formed within narrower temperature ranges. The gold–telluride–quartz assemblage was deposited between 325 and 175 °C, while the telluride–sulfide–quartz formed between 219 and 258 °C. Possible influx of meteoric waters led to progressive cooling and a decrease in salinity from the early to late fluid generations during mineral deposition. Overall data on ore and associated with metasomatic alteration mineralogy indicate that the ore formation occurred under relatively reduced or neutral conditions from weakly acidic to near-neutral aqueous solutions, possessing relatively high sulfur and tellurium fugacity. Full article

A number of Cd-, Pb-, Ag- and Sb(±As)-bearing minerals are found in the Zn-rich smoker chimneys of the Irinovskoe hydrothermal sulfide field, 13°20′ N, Mid-Atlantic Ridge. Sulfide samples were studied using optical microscopy, SEM/EDS, XRD, EBDS, ICP-MS and thermodynamic approaches. The chimneys consist of major sphalerite (including Cd-bearing type with up to 41.38 wt% Cd) and wurtzite, subordinate opal, pyrite, chalcopyrite and Fe-oxyhydroxides, as well as accessory native sulfur, baryte, secondary copper sulfides, galena, CdS phase (most likely hawleyite), pyrrhotite, isocubanite, acanthite, Ag–Cu–Sb(±As)-bearing minerals, native gold, anglesite, gypsum, smectites, naumannite and lollingite. The main source of metals for the formation of Zn-rich sulfides was mafic rocks, with a subordinate role from ultramafic rocks. Crystallization of most accessory minerals at low temperatures (<120 °C) under acidic/reducing conditions and low S activity could be initiated by a magmatic input, which is supported by a negative S isotopic composition of bulk sulfide samples. The finding of Cd-rich sphalerite and a CdS phase in low-temperature mineral assemblage significantly expands the temperature limits of their possible formation. The high Cd contents of easily soluble sphalerite and the presence of the CdS phase should be taken into account in possible future mining and processing of seafloor hydrothermal sulfide fields. Full article

Gold-silver mineralization in the Rodnikovoe LS epithermal deposit is characterized by selenium speciation. Two main alternating ore assemblages have been identified: silver-aguilarite-acanthite and gold-uytenbogaardtite-acanthite. The former mineral association is intergrown with secondary silver (Ag_0.77–0.91), whereas the latter assemblage is closely associated with high-grade gold (Au_0.63–0.67). However, both are dominated by Ag_0.49–0.56Au_0.44–0.51 alloys. The geochemical evolution of the ore-forming system developed in the direction: Fe → Cu; Ag → Au; S → Se; As → Sb. Organic compounds (1 relative %) of both biogenic and thermogenic origin were found in fluid inclusions. These molecules participated in the formation of Ag,Au-complexes and transported noble metals along with selenium. Hydrothermal fluids are characterized by fSe₂/fS₂ ratios < 1, conditions such that the deposition of selenide minerals is inhibited, except for the naumannite and acanthite series. These conditions allow active entry of selenium into sulfosalts (the selenium substitutes for sulfur). Full article

The mineral and chemical compositions of ores from the Corrida epithermal Au-Ag deposit (Chukchi Peninsula, Russia) were studied using the optical and scanning electron microscopy with X-ray energy-dispersion microanalysis. The deposit was formed at the time close to the period when the basic volume of acid magmas had been emplaced within the Okhotsk–Chukotka belt (84 to 80 Ma). The Au–Ag mineralization is distinguished with Au-Ag sulphides and selenides (uytenbogaardtite-fischesserite solid solution, Se-acanthite, S-naumannite) and Ag halides of the chlorargyrite-embolite-bromargyrite series. The ores were formed in two stages. Using microthermometric methods, it has been established that the ore-bearing quartz was formed in the medium-temperature environment (340–160 °C) with the participation of low-salt (3.55 to 0.18 wt.% NaCl eq.) hydrotherms, mostly of the NaCl composition with magnesium, iron and low-density СО₂. According to our results of thermodynamic modeling at temperatures from 300 to 25 °C and data on mineral metasomatic alterations of the host rocks, the Au-Ag-S-Se-Cl-Br mineralization was formed at decreasing temperature and fugacity of sulphur (logƒS₂ from −6 to −27), selenium (logƒSe₂ from −14 to −35), and oxygen (logƒО₂ from −36 to −62), with near-neutral solutions replaced by acid solutions. Analysis of the obtained data shows that the Corrida refers to the group of the LS-type epithermal deposits. This deposit is a new example of epithermal deposits with significant quantities of Au–Ag chalcogenides (acanthite, uytenbogaardtite, fischesserite, naumannite and others). Full article

Tilkerodeite, ideally Pd₂HgSe₃, is a new platinum-group selenide from the Eskaborner Stollen (Adit Eskaborn) at Tilkerode, Harz Mountains, Germany. Tilkerodeite crystals occur as euhedral inclusions in tiemannite or as extremely fine-grained lamellar aggregates (grain-size up to 3 μm) in a dolomite–ankerite matrix, together with clausthalite, tiemannite, jacutingaite, stibiopalladinite, and native gold. Neighbouring Se-bearing minerals include tischendorfite and chrisstanleyite. Tilkerodeite is opaque with a metallic luster, and is flexible in blade-like crystals, with perfect basal cleavage $\left\{001\right\}$. In plane-polarized light, tilkerodeite is brownish-grey. It is weakly bireflectant, and weakly pleochroic in shades of light-brown and grey. The anisotropy is weak, with rotation tints in weak shades of greenish-brown and grey-brown. The range of reflectance is estimated in comparison to clausthalite with 45–50%. Electron-microprobe analyses yield the mean composition (wt. %) Se 32.68, Hg 26.33, Pt 20.62, Pd 15.89, Pb 2.72, Cu 0.66, S 0.27, total 99.17 wt. %. The empirical formula (based on six atoms pfu) is (Pd_1.08Pt_0.76Pb_0.09Cu_0.07)_Σ2.00Hg_0.95(Se_2.98S_0.07)_Σ3.05. The ideal formula is Pd₂HgSe₃. Tilkerodeite is trigonal, with Pt₄Tl₂Te₆-type structure, space group P$\bar{3}$m1, a = 7.325(9) Å, c = 5.288(6) Å, V = 245.7(9) ų, and Z = 2. It is the Pd-analogue of jacutingaite. Tilkerodeite formed hydrothermally, possibly involving the alteration of tiemannite by low-temperature oxidizing fluids. The new species has been approved by the IMA-CNMNC (2019-111) and is named after the locality. Tilkerode is the most important selenide-bearing occurrence in Germany and type locality of naumannite, eskebornite, and tischendorfite. Full article

Significant selenium enrichment associated with selenides and previously unknown Ag-Pb-Sb, Ag-Sb and Pb-Sb sulfosalts has been discovered in hydrothermal ore veins in the Anthony of Padua mine near Poličany, Kutná Hora ore district, central Bohemia, Czech Republic. The ore mineralogy and crystal chemistry of more than twenty silver minerals are studied here. Selenium mineralization is evidenced by a) the occurrence of selenium minerals, and b) significantly increased selenium contents in sulfosalts. Identified selenium minerals include aguilarite and selenides naumannite and clausthalite. The previously unknown sulfosalts from Kutná Hora are identified: Ag-excess fizélyite, fizélyite, andorite IV, andorite VI, unnamed Ag-poor Ag-Pb-Sb sulfosalts, semseyite, stephanite, polybasite, unnamed Ag-Cu-S mineral phases and uytenbogaardtite. Among the newly identified sulfides is argyrodite; germanium is a new chemical element in geochemistry of Kutná Hora. Three types of ore were recognized in the vein assemblage: the Pb-rich black ore (i) in quartz; the Ag-rich red ore (ii) in kutnohorite-quartz gangue; and the Ag-rich ore (iii) in milky quartz without sulfides. The general succession scheme runs for the Pb-rich black ore (i) as follows: galena – boulangerite (– jamesonite) – owyheeite – fizélyite – Ag-exces fizélyite – andorite IV – andorite VI – freieslebenite – diaphorite – miargyrite – freibergite. For the Ag-rich red ore (ii) and ore (iii) the most prominent pattern is: galena – diaphorite – freibergite – miargyrite – pyragyrite – stephanite – polybasite – acanthite. The parallel succession scheme progresses from Se-poor to Se-rich phases, i.e., galena – members of galena – clausthalite solid solution – clausthalite; miargyrite – Se-rich miargyrite; acanthite – aguilarite – naumannite. A likely source of selenium is in the serpentinized ultrabasic bodies, known in the area of “silver” lodes in the South of the ore district, which may enable to pre-concentrate selenium, released into hydrothermal fluids during tectonic events. The origin of the studied ore mineralization is primarily bound to the youngest stage of mineralization of the whole ore district, corresponding to the Ag-Sb sequence of the ‘eb’ ore type of the Freiberg ore district in Saxony (Germany) and shows mineralogical and geochemical similarities to low-sulfidation epithermal-style Ag-Au mineralization. Full article

Selenium-rich Au–Ag mineralization has been discovered in the Kremnica ore district, central Slovakia. The mineralization is hosted by a single quartz–dolomite vein hosted by Neogene propyllitized andesites of the Kremnica stratovolcano. Ore mineralogy and crystal chemistry of individual ore minerals have been studied here. The early base-metal ore mineralization composed of pyrite, sphalerite, and chalcopyrite lacks selenium, whereas the superimposed Au–Ag paragenesis is Se-enriched. The Au–Ag alloys, uytenbogaardtite, minerals of the galena–clausthalite series, acanthite–naumannite series, diaphorite, miargyrite, pyrargyrite–proustite, polybasite group, minerals of the tetrahedrite group and andorite branch (andorite IV, andorite VI, Ag-excess fizélyite), freieslebenite, and rare Pb–Sb sulphosalts (scaiinite, robinsonite, plagionite) have been identified here. Besides selenides, the most Se-enriched phases are miargyrite, proustite–pyrargyrite, and polybasite–pearceite, whose Se contents are among the highest reported worldwide. In addition, one new phase has been found, corresponding to a Se-analogue of pearceite containing 2.08–3.54 apfu Se. The style of mineralization, paragenetic situation, and chemical trends observed in individual minerals are comparable to those of Au–Ag low-sulphidation epithermal Au–Ag mineralizations of the Kremnica and neighboring Štiavnica and Hodruša-Hámre ore districts. However, the pronounced enrichment in selenium is a specific feature of the studied vein only. Full article

Silica sinters forming at the Wairakei geothermal power plant in New Zealand are composed of noncrystalline opal-A that deposited rapidly from cooling geothermal liquids flashed to atmosphere. The sinter is laminated with alternating layers of variably compacted silicified filamentous microbes encased by chains of fused silica microspheres. Microscopic inspection of bonanza quartz vein samples from the Buckskin National low-sulfidation epithermal precious metal deposit in Nevada showed that colloform bands in these veins exhibit relic microsphere textures similar to those observed in the silica sinters from the Wairakei power plant. The textural similarity suggests that the colloform bands were originally composed of noncrystalline opal-A that subsequently recrystallized to quartz. The colloform bands contain dendrites of electrum and naumannite that must have grown in a yielding matrix of silica microspheres deposited at the same time as the ore minerals, implying that the noncrystalline silica exhibited a gel-like behavior. Quartz bands having other textural characteristics in the crustiform veins lack ore minerals. This suggests that ore deposition and the formation of the colloform bands originally composed of compacted microspheres of noncrystalline silica are genetically linked and that ore deposition within the bonanza veins was only episodic. Supersaturation of silica and precious metals leading to the formation of the colloform bands may have occurred in response to transient flashing of the hydrothermal liquids. Flashing of geothermal liquids may thus represent a key mechanism in the formation of bonanza precious metal grades in low-sulfidation epithermal deposits. Full article

The Sierra de Cacheuta vein-type Se mineralization in the Mendoza Province predominantly consists of clausthalite, klockmannite, eskebornite, eucairite, and naumannite. These primary selenides formed in a fault zone, cutting through fine-grained trachytic host rock. Cross-sections perpendicular to the veinlets, polarized light microscopy, and scanning-electron microscopy, combined with electron-microprobe analysis, provide a record of the relationship between different crystallization and deformation events. Mineralization encompasses four episodes of fault formation (d1–d4): early zonal selenide crystallization (stage (I)); ductile deformation of the selenides (stage (II)); fault re-opening, fluid-mediated metal mobilization, metalliferous-fluid infiltration, and mineral precipitation (stage (III)); and subsequent alteration (stage (IV)). The Se vein originated from multiple injections of highly oxidized, metal-rich fluids. These low-T solutions (estimated max. temperature 100 °C, max. pressure 1 bar) possessed high to exceptionally high Se fugacities (log f_Se2 between −14.5 and −11.2) that prevailed for most of the evolution of the deposit. The source of the Se and the accompanying metals (Cu, Ag, Pb, and Fe) is probably the neighboring bituminous shale. The deposition of Se minerals occurred when the oxidized metal-bearing solutions came in contact with a reductant, which caused the reduction of mobile selenate to immobile selenide or elemental Se. We identified several features that permit us to safely distinguish samples from Cacheuta from Argentinian Se deposits in the Province of La Rioja: (I) trachytic host rock fragments containing bitumen and TiO₂ pseudomorphs after titanomagnetite; (II) early Co-rich and Ni-poor krut’aite (Co < 6.7 wt %, Ni < 1.2 wt %) partly replaced by clausthalite, umangite, klockmannite, eskebornite, Ni-poor tyrrellite (Ni < 2.7 wt %), Ni-poor trogtalite (Ni < 1.2 wt %), and end-member krut’aite and petříčekite; (III) lack of calcite gangue; and (VI) Se-bearing alteration minerals comprising chalcomenite, molybdomenite, cobaltomenite, an unnamed Cu selenide (for which the ideal formula may be either Cu₂Se₃ or Cu₅Se₈), and possibly mandarinoite, mereheadite, orlandiite, and scotlandite as new species for this occurrence. Full article

Selenium mineralization in the Příbram uranium and base-metal district (Central Bohemia, Czech Republic) bound to uraninite occurrences in calcite hydrothermal veins is extremely diverse. The selenides antimonselite, athabascaite, bellidoite, berzelianite, brodtkorbite, bukovite, bytízite, cadmoselite, chaméanite, clausthalite, crookesite, dzharkenite, eskebornite, eucairite, ferroselite, giraudite, hakite, klockmannite, naumannite, permingeatite, příbramite, sabatierite, tiemannite, and umangite were found here, including two new mineral phases: Hg-Cu-Sb and Cu-As selenides. Those selenides—and in some cases their sulphidic equivalents—are characterized using wavelength-dispersive spectroscopy, reflected light, powder X-ray diffraction, single crystal X-ray diffraction, Raman spectroscopy, and electron backscatter diffraction. The selenide mineralization in the Příbram uranium district is bound to the border of the carbonate-uraninite and subsequent carbonate-sulphidic stages. Selenides crystallized there at temperatures near 100 °C in the neutral-to-weakly-alkaline environment from solutions with high oxygen fugacity and a high Se₂/S₂ fugacity ratio. Full article

Tertiary low sulfidation (LS) epithermal deposits in the western USA often show evidence of the former presence of nanoparticle-sized precious-metal and silica phases in the highest grade (bonanza) ores. Here, nanoparticles are defined to have a size less than ~10⁻⁷ m. The ore-mineral textures that formed from aggregation of nanoparticles (or colloids) observed to date in these ores include electrum and naumannite (Ag₂Se). Here it is proposed that chalcopyrite also forms nanoparticles in these ores, but sulfide nanoparticles apparently have significantly different physical (surface) properties than the precious-metal phases, and thus exhibit different mineral textures (e.g., no textural evidence of previous chalcopyrite nanoparticles). Textures described here show that nanoparticles of precious-metal phases and silica were episodically and often repeatedly deposited to form the banded bonanza veins typical of many western USA epithermal deposits. Chalcopyrite is the most abundant metal-sulfide mineral in these bonanza ores, and it was also deposited episodically as well, and it appears to replace earlier formed naumannite dendrites. However, this apparent “replacement” texture may just be the result of naumannite dendrite limbs trapping chalcopyrite nanoparticles that later recrystallized to the apparent replacement texture. The episodic and repetitive nature of the metal-depositing events may record periodic “degassing” of magma chambers at depth, where metals are repeatedly delivered to the shallow epithermal environment by “vapor-phase” metal (loid) transport. Full article