scholarly journals A Combined EPMA and LA-ICP-MS Investigation on Bi-Cu-Au Mineralization from the Kizhnica Ore Field (Vardar Zone, Kosovo)

Minerals ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1223
Author(s):  
Sławomir Mederski ◽  
Jaroslav Pršek ◽  
Dimitrina Dimitrova ◽  
Bahri Hyseni

This paper describes a newly discovered Bi-Cu ± Au mineralization co-occurring with Pb-Zn-Ag hydrothermal mineralization within the Kizhnica-Hajvalia-Badovc ore field, central Kosovo, Vardar Zone. The mineralogy of two styles of Bi-Cu ± Au mineralization was described using EPMA in combination with reflected and transmitted light microscopy. Hydrothermal Cu-Bi veinlets in the Kizhnica andesite quarry consist of Bi sulfosalts (bismuthinite, cosalite, aikinite, and krupkaite), pyrite, hematite, chalcopyrite, galena, sphalerite, and tetrahedrite group minerals. Disseminated Bi-Au-Cu-Te mineralization from the contact type of mineralization (hornfels) consists of Bi sulfosalts (cannizzarite, bismuthinite, galenobismutite, cosalite), associated with sulfarsenides (arsenopyrite, gersdorffite, and cobaltite), base metal sulfides (chalcopyrite, pyrite, sphalerite, pyrrhotite, and galena), native gold, native bismuth, and tetradymite. LA-ICP-MS analyses of sphalerite, chalcopyrite, and tetrahedrite indicate increased content of In and Sn in the Kizhnica Bi-Cu-Au mineralizing system, while LA-ICP-MS analyses in pyrites show the presence of many elements, e.g., Au, As, Co, Sb, Tl, Hg, Pb, Bi related to the structure of pyrite or controlled by nano-inclusions. The results suggest a connection between Bi-Cu±Au mineralization and the proximity to intrusive rocks, which may be helpful for Au exploration in Kosovo.

2021 ◽  
Author(s):  
Elena-Luisa Iatan

<p>Voia deposit belongs to the Săcărâmb-Cetraș-Cordurea Miocene volcano-tectonic alignment of the South Apuseni Mountains, Romania. This large volcanic complex represents a Sarmatian-Pannonian magmatic-hydrothemal mega-system of around 5 km<sup>2</sup> with an estimated 3–4 Ma time-space evolution, consisting of seven andesitic volcanic structures grouped in a circle, three subvolcanic andesite-quartz porphyry microdiorite and associated porphyry Cu-Au(Mo), pyrite Ca-Mg skarns and epithermal Au-Ag-Pb-Zn-Cu mineralizations.</p><p>The mineral assemblages of alteration and mineralization processes belong to several mineralized zones on a vertical scale, according to sampling evidence and laboratory studies. HS products are found in the upper part of the structure (300-500 m), with dominant advanced and intermediate argillic alterations and sulfide-sulfate gold-poor veins (pyrite, marcasite, base metal sulfides, Fe-Ti oxides, vuggy quartz, alunite, gypsum, anhydrite). Within the 500-1200 m depth, the HS mineral assemblages gradually decrease in favor of IS and LS products. It is characterized by the coexistence of gold-rich LS assemblage (native gold, base metal sulfide, adularia, sericite-illite, chlorite, carbonates ± anhydrite veins), with the IS assemblage (iron oxides, chalcopyrite, pyrite, quartz, anhydrite). These assemblages overprint the HS mineral associations, resulting in a transition zone characterized by gold - pyrite - chalcopyrite - iron oxides - quartz - anhydrite mineral assemblage characteristic for HS and native gold - pyrite - base metal sulfides - carbonates - quartz mineral assemblage corresponding to IS+LS type.</p><p>Gold is present in all of the identified mineralization forms: porphyry-epithermal Cu-Au, epi-mesothermal carbonate veins with gold - base metal sulfides, quartz veins with pyrite - chalcopyrite - magnetite ± hematite ± anhydrite, anhydrite veins with base metal sulfides and sulfosalts, anhydrite veins with pyrite - anhydrite ± quartz, vuggy quartz (silica residue) with gold-poor pyrite veins and impregnations in porphyry systems.</p><p>Drilling core samples revealed that in Voia deposit, gold is concentrated in chalcopyrite (drills no. 7, 19, 37) along with pyrite - magnetite - hematite - quartz assemblage from the late potassic stage. The major amount of gold associated with chalcopyrite tends to be mainly submicroscopic. Pyrite from anhydrite veins of the early potassic stage ± phyllic alteration is relatively poor in gold (drills no. 1-6, 8-14). However, the highest gold contents are present in pentagonal dodecahedron pyrites (drills no. 33, 38, 39) of pyrite-chalcopyrite-magnetite ± hematite-quartz assemblage from late potassic stage ± phyllic alteration. Pyrite associated with magnetite from anhydrite veins tends to be poor in gold (drills no. 8, 11, 15, 28, 29). A carbonate vein containing gold-bearing base metal sulfides that was intercepted at 960,00-960,30m depth by drill no. 17 is one of the richest in gold.</p><p>Native gold occurs as fine inclusions in ore minerals (5-20 μm). Large irregular grains of native gold (>50 μm) appear at mineral boundaries and along the fissures. The gold color is bright yellow and has a measured Au:Ag ratio of 5:1, suggesting that native gold has been formed at a relatively high temperature.</p><p>Acknowledgments: This work was supported by two Romanian Ministry of Research and Innovation grants: PN-III-P4-ID-PCCF-2016-4-0014 and PN-III-P1-1.2-PCCDI-2017-0346/29.</p>


Minerals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 18
Author(s):  
Nadezhda Tolstykh ◽  
Valeriya Brovchenko ◽  
Viktor Rad’ko ◽  
Maria Shapovalova ◽  
Vera Abramova ◽  
...  

Pyrrhotite (or Cu-poor) massive ores of the Skalisty mine located in Siberia, Russia, are unique in terms of their geochemical features. These ores are Ni-rich with Ni/Cu ratios in the range 1.3–1.9 and contain up to 12.25 ppm Ir + Rh + Ru in bulk composition, one of the highest IPGE contents for the Norilsk-Talnakh ore camp. The reasons behind such significant IPGE Contents cannot simply be explained by the influence of discrete platinum-group minerals on the final bulk composition of IPGE because only inclusions of Pd minerals such as menshikovite, majakite, and mertieite II in Pd-maucherite were observed. According to LA-ICP-MS data obtained, base metal sulfides such as pyrrhotite, pentlandite, and pyrite contain IPGE as the trace elements. The most significant IPGE concentrator being Py, which occurs only in the least fractionated ores, and contains Os up to 4.8 ppm, Ir about 6.9 ppm, Ru about 38.3 ppm, Rh about 36 ppm, and Pt about 62.6 ppm. High IPGE contents in the sulfide melt may be due to high degrees of partial melting of the mantle, interaction with several low-grade IPGE impulses of magma, and (or) fractionation of the sulfide melt in the magma chamber.


2021 ◽  
Vol 130 ◽  
pp. 103945
Author(s):  
Chen Wei ◽  
Lin Ye ◽  
Yusi Hu ◽  
Zhilong Huang ◽  
Leonid Danyushevsky ◽  
...  

2021 ◽  
Author(s):  
Ling Tan ◽  
Thomas Jones ◽  
Jianping Xie ◽  
Xinxing Liu ◽  
Gordon Southam

Abstract Weathering of the Merensky reef was enhanced under laboratory conditions by Fe- and S-oxidizing bacteria: Acidithiobacillus ferrooxidans, Acidithiobacillus thiooxidans, and Leptospirillum ferrooxidans. These bacteria preferentially colonized pyrrhotite and pyrite, versus pentlandite and chalcopyrite (all of which were common within the rock substrate), promoting weathering. Weathering of base metal sulfides resulted in the precipitation of Fe oxides, Fe phosphate, and elemental sulfur as secondary minerals. Fe pyroxene weathered readily under acidic conditions and resulted in mineral dissolution, while other silicates (orthopyroxene and plagio-clase) precipitated Fe phosphate spherules or coatings on their surface. The deterioration of the platinum group metal (PGM) matrix (base metal sulfides and silicates) and the occurrence of a platinum grain associated with platinum nanoparticles observed in the biotic thin sections demonstrate that biogeochemical acid weathering is an important step in the active release of intact PGM grains. A platinum grain embedded in secondary Fe oxides/phosphate that had settled by gravity within the weathering solution demonstrates that secondary minerals that formed during weathering of PGM-hosting minerals also represent targets in PGM exploration by trapping and potentially slowing PGM migration. Dispersion halos surrounding or occurring downstream from PGM occurrences will likely produce two physical target classes—i.e., grains and colloids—under surficial weathering conditions.


2008 ◽  
Vol 72 (4) ◽  
pp. 953-970 ◽  
Author(s):  
T. Oberthür ◽  
T. W. Weiser

AbstractGold mineralization at the Viceroy Mine is hosted in extensional veins in steep shear zones that transect metabasalts of the Archaean Arcturus Formation. The gold mineralization is generally made up of banded or massive quartz carrying abundant coarse arsenopyrite. However, most striking is a distinct suite of Au-Bi-Te-S minerals, namely joseite-A (Bi4TeS2), joseite-B (Bi4Te2S), hedleyite (Bi7Te3), ikunolite (Bi4S3), ‘protojoseite’ (Bi3TeS), an unnamed mineral (Bi6Te2S), bismuthinite (Bi2S3), native Bi, native gold, maldonite (Au2Bi), and jonassonite (AuBi5S4). The majority of the Bi-Te-S phases is characterized by Bi/(Se+Te) ratios of >1. Accordingly, this assemblage formed at reduced conditions at relatively low fS2 and fTe2. Fluid-inclusion thermometry indicates depositional temperatures of the main stage of mineralization of up to 342°C, in the normal range of mesothermal, orogenic gold deposits worldwide. However, melting temperatures of Au-Bi-Te phases down to at least 235°C (assemblage (Au2Bi + Bi + Bi7Te3)) imply that the Au-Bi-Te phases have been present as liquids or melt droplets. Furthermore, the close association of native gold, native bismuth and other Bi-Te-S phases suggests that gold was scavenged from the hydrothermal fluids by Bi-Te-S liquids or melts. It is concluded that a liquid/melt-collecting mechanism was probably active at Viceroy Mine, where the distinct Au-Bi-Te-S assemblage either formed late as part of the main, arsenopyrite-dominated mineralization, or it represents a different mineralization event, related to rejuvenation of the shear system. In either case, some of the gold may have been extracted from pre-existing, gold-bearing arsenopyrite by Bi-Te-S melts, thus leading to an upgrade of the gold ores at Viceroy. The Au-Bi-Te-S assemblage represents an epithermal-style mineralization overprinted on an otherwise mesothermal (orogenic) gold mineralization.


Author(s):  
John D. Greenough ◽  
Alejandro Velasquez ◽  
Mohamed Shaheen ◽  
Joel Gagnon ◽  
Brian J. Fryer ◽  
...  

Trace elements in native gold provide a “fingerprint” that tends to be unique to individual gold deposits. Fingerprinting can distinguish gold sources and potentially yield insights into geochemical processes operating during gold deposit formation. Native gold grains come from three historical gold ore deposits; Hollinger, McIntyre (quartz-vein ore), and Aunor near Timmins, Ontario, at the western end of the Porcupine gold camp and the south-western part of the Abitibi greenstone belt. Laser-ablation, inductively-coupled plasma mass spectrometry (LA ICP MS) trace element concentrations were determined on 20 to 25 µm wide, 300 µm long rastor trails in ~ 60 native gold grains. Analyses used Ag as an internal standard with Ag and Au determined by a scanning electron microscope with an energy dispersive spectrometer. The London Bullion Market AuRM2 reference material served as the external standard for 21 trace element analytes (Al, As, Bi, Ca, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Pd, Pt, Rh, Sb, Se, Si, Sn, Te, Ti, Zn; Se generally below detection in samples). Trace elements in native gold associate according to Goldschmidt’s classification of elements strongly suggesting that element behavior in native Au is not random. Such element behavior suggests that samples from each Timmins deposit formed under similar but slightly variable geochemical conditions. Chalcophile and siderophile elements provide the most compelling fingerprints of the three ore deposits and appear to be mostly in solid solution in Au. Lithophile elements are not very useful for distinguishing these deposits and element ABSTRACT CUT OFF BY SOFTWARE


2010 ◽  
pp. 115-135

Abstract Transmitted-light methods reveal more details of the morphology of fiber-reinforced polymeric composites than are observable using any other available microscopy techniques. This chapter describes the various aspects relating to the selection and preparation of ultrathin-section specimens of fiber-reinforced polymeric composites for examination by transmitted-light microscopy techniques. The preparation steps covered are a selection of the rough section, preparation of the rough section for preliminary mounting, grinding and polishing the primary-mount first surface, mounting the first surface on a glass slide, and preparing the second surface (top surface). The optimization of microscope conditions and analysis of specimens by microscopy techniques are also covered. In addition, examples of composite ultrathin sections that are analyzed using transmitted-light microscopy contrast methods are shown throughout.


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