The Oktyabrsk PGE-Cu-Ni deposit is one of the largest resources in the Norilsk–Talnakh ore district, Russia, and it is viewed as an ore giant on a global scale. It contains three types of ores: massive, disseminated and veinlet-disseminated. The two former ore types were formed by a liquation process, whereas the latter was associated with fluid-induced selective metasomatic replacement of metamorphosed wall rocks. One of the major ore minerals in all ore types is chalcopyrite. In this study, we determined concentrations of trace elements in this mineral using laser ablation inductively coupled plasma mass spectrometry. It appeared that standard geochemical tools, such as plotting the data in the form of diagrams of normalized concentrations, binary and ternary plots, do not allow one to distinguish chalcopyrite from visually and genetically different ore types. In contrast, more advanced statistical methods such as cluster analysis show different groupings of elements for each ore type. Based on the element clustering, a classification tree was suggested, which allowed for the differentiation of massive, disseminated and veinlet-disseminated ore types of the Oktyabrsk deposit by Se, Te, Cd and Pb concentrations in chalcopyrite with a success rate of 86%. The general feature is that chalcopyrite of veinlet-disseminated ore is poorer in these elements compared to chalcopyrite of the two other ore types. Chalcopyrite of massive ore is poorer in Se and Te when compared to chalcopyrite of disseminated ore.

This study considers the features of the chemical composition, internal structure, and oscillatory zoning of sulfosalts and sulfates in the epithermal high–intermediate-sulfidation-type Au-Ag-Te Emmy deposit (Khabarovsk Territory, Russia). In Emmy deposit, sulfosalts primarily represent goldfieldite, probably corresponding to a high-sulfidation (HS) mineral association replaced bytennantite–tetrahedrite group minerals. The latter is associated with tellurides and native tellurium, corresponding to an intermediate-sulfidation (IS)-type ore assemblage and suggesting an increasing influx of Te, Sb, and As in the system. Goldfieldite is replaced by native tellurium and tellurides along its growth zones, and is characterized by oscillatory zoning. The replacement of goldfieldite by mercury, nickel, lead, and copper tellurides indicate a new influx of native gold, native tellurium, and gold–silver tellurides into the open mineral-forming system. At deeper levels of the Emmy deposit, an advanced argillic alteration assemblage includes aluminum phosphate–sulfate (APS) minerals, represented by members of the svanbergite–woodhouseite series. Element mapping of the studied APS mineral grains indicated three distinct areas recording the evolution of the hydrothermal system in the Emmy: an oscillatory-zoned margin enriched in sulfur, lead, and barium, corresponding to the late influx of IS state fluids related to gold and tellurides; an intermediate part, which is leached and corresponds to the HS mineralization stage; and the central part of the grains, which is enriched in cerium, calcium, and strontium, resulting from a replacement of magmatic apatite in the pre-ore alteration stage. The leached zone between the core and rim of the APS grains is related to a change in crystallization conditions, possibly due to the mixing processes of the fluids with meteoric water. Barite, found in the upper level of the advanced argillic hypogene alteration assemblage, is also characterized by oscillatory zoning, associated with the enrichment of individual zones in lead. Micron gold particles associated with barite are confined to their lead-enriched zones. The study of fluid inclusions in quartz within the Emmy deposit showed the hydrothermal ore process at a temperature of 236–337 °C. Homogenization temperatures for quartz–pyrite–goldfieldite mineral association vary within 337–310 °C and salinity varies within 0–0.18 wt.%NaCl equivalent, and for gold–silver–telluride–polymetallic mineral association, they decrease and vary within 275–236 °C and salinity slightly increases from 0.18 to 0.35 wt.%NaCl equivalent. This study demonstrates that the nature of oscillatory zoning in sulfosalts and sulfates in the Emmy deposit results from an external process. Such a process is of fundamental importance from a genetic point of view.

Strizhkovskoe barite-polymetallic deposit is a typical medium-low-temperature hydrothermal-metasomatic deposit. It’s located within north-west part of Zmeinogorsk-Bystrushinskiy downfold; host rocks are volcano-terrigenous Devonian rocks. Ore bodies are related to sublatitudinal and submeridional faults intercrossing. Wallrock quartz-chlorite-sericite metasomatites formed prior to ores formation. Ore mineralization process began in Middle Devonian. Main ore minerals are sphalerite, galena, and chalcopyrite. Also there are gold and silver occurring as electrum, acanthite; silver is present in fahlores as an isomorphous admixture. Formation of the deposit subdivides into two main stages and five phases; according to obtained results of isotope study of the sulfides, it’s possible to conclude that there was a mixed source of ore matter (mantle source replacing with crust source). The temperature of main ore formation stage varied form 230 to 180 degrees. Solutions salinity varied from 9 to 15 % wt of NaCl equiv. According to fluid inclusions study results, the solutions consisted of water and following compounds CO₂, NH₃, SO₂, HCO₃.

This study considers the features of the chemical composition, internal structure, and oscillatory zoning of sulfides, sulfosalts and sulfates in the epithermal high-intermediate sulfidation type Au-Ag-Te Emmy deposit (Khabarovsk Territory), Russia. In this deposit the most widespread sulfide is pyrite occurring in two generations: pre-ore pure pyrite (I) with cubic crystal habit and dimensions from 20 μm to 0.5 mm from the early barren pre-ore hydrothermal stage, and pyrite (II) of the ore stage, which is represented by (a) colloform aggregates (IIa) formed as a result of rapid precipitation from the solution, and (b) crystalline pyrite (IIb), which is precipitated due to continuous decrease in temperature. Both pyrite (II) morphological varieties contain copper (0.06-6.03 wt.%). The crystalline variety of pyrite is associated with goldfieldite, hemusite and kawazulite which were deposited during the early mineralizing event in the deposit.

Zmeinogorsky ore district is located in the northwest part of Ore Altai megatrough, which has long-lasting history of its development and complicated geological structure. Within the ore district, which is the northwest part of the devonian Zmeinogorsk-Bystrushinsky trough, ore mineralization is associated with the system of northwest border faults and cross branch faults. There were four main stages and five phases of minerogenesis. The first stage is the stage of oregenesis beginning and quartz-chlorite-sericite wall-rock alteration rocks formation. Ore deposition and intense tectonics took place during the second stage. The third stage is the most longstanding and productive ore formation stage. There are five distinct minerogenesis phases within this stage. The fourth stage expressed in erosion development and supergene alteration of already formed ore bodies with oxidation zone formation. Main ore minerals are pyrite, chalcopyrite, sphalerite and galena. Minor minerals are tetrahedrite, bornite, tennantite and chalcocite. Precious metals minerals are acanthite, gold, electrum, gold and silver amalgams. Barren minerals are barite, quartz, calcite, gypsum. According to obtained data average isotopic composition of third stage sulphides is: pyrite -0,2‰, chalcopyrite 0‰, galena +0,5‰, sphalerite -1,2‰ for the first complex; chalcopyrite -1,9‰, galena -3,4‰, sphalerite -2,3‰, tetrahedrite -3,7‰ for the second complex; tennantite -12,8‰, bornite -8,9‰ for the third complex. Sulfur isotopic compoisiton variations indicate source inhomogeneity. Thus, there was dominant source change from mantle one in the beginning to crustal one in the end. Main oregenesis stages took place in the range of temperatures between 170 and 210°С and in the mineral-forming solutions salinity range between 3 and 10 wt % NaCl equiv.