Loypishnyun Low-Sulfide Pt–Pd Deposit of the Monchetundra Basic Massif,Kola Peninsula,Russia

The geology of the basal-structural Loypishnyun low-sulfide Pt–Pd deposit is characterized, including its mineral composition and the peculiarities of its PGE and chalcophile-element distribution in ore. The deposit is situated in the northeastern part of the Monchetundra basic massif and is localized in its lower norite–orthopyroxenite zone, intensely injected with late gabbroic rocks. Two ore zones are distinguished within the deposit. Ore zone 1 has been traced by drilling for about 1.5 km at a thickness from 10–15 to 120 m and incorporates from two to nine separate lenticular–sheetlike orebodies 0.5–25 m in thickness. Ore zone 2 has been traced for 550 m and is represented by one orebody 5–35 m thick. The internal structure of the orebodies is characterized by alternation of low-grade (Pt + Pd = 0.5–0.9 gpt), ordinary (Pt + Pd = 1.0–1.9 gpt), and high-grade (Pt + Pd > 2 gpt) interlayers of various thickness. The ores are spatially and genetically related to sulfide mineralization (pentlandite–chalcopyrite–pyrrhotite) in an amount of 1–5 vol %. The PGE distribution in ores normalized to primitive mantle is characterized by fractionation of easily fusible platinoids with a positive Pd anomaly. The spectra of chalcophile elements normalized to primitive mantle are notable for elevated Te, Bi, As, and Se contents with respect to Sn, Hg, and Pb, which reflects the significant contribution of Te, Bi, and As in the formation of platinum group minerals (PGM), whereas Se, which is devoid of proper mineral phases, most likely is an admixture in the composition of sulfides. The S/Se value in ore of the Loypishnyun deposit varies from 31 to 814. The platinum group elements (PGE) in ore are represented by 45 noble metal minerals. Ore zone 1 is characterized by lateral mineral zoning, which is expressed as replacement of a bismuthotelluride–sulfide PGM assemblage by an assemblage of copper–PGE compounds and alloys. In ore zone 2, a mineral assemblage of tellurides, copper–PGE compounds and alloys predominates, with native gold, silver, and palladium, as well as sulfides and bismuthotellurides, playing a subordinate role. The formation of PGM ore proceeded under variable sulfur fugacity conditions, beginning with the late magmatic stage at temperatures of 900–700°C and ending with hydrothermal transformation at a temperature of <500°C.     

Mud Volcanic Fluids of the Kerch–Taman Region: Geochemical Reconstructions and Regional Trends. Communication 1: Geochemical Features and Genesis of Mud-Volcanic Waters

Lithology and Mineral Resources - The chemical and isotopic characteristics (δ18O and δ2H) of water from 42 mud volcanoes of the Kerch–Taman region (Crimean–Caucasus district)...     

Behavior of uranium under conditions of interaction of rocks and ores with subsurface water

The behavior of uranium during interaction of subsurface water with crystalline rocks and uranium ores is considered in connection with the problem of safe underground insulation of spent nuclear fuel (SNF). Since subsurface water interacts with crystalline rocks formed at a high temperature, the mineral composition of these rocks and uranium species therein are thermodynamically unstable. Therefore, reactions directed toward the establishment of equilibrium proceed in the water-rock system. At great depths that are characterized by hindered water exchange, where subsurface water acquires near-neutral and reducing properties, the interaction is extremely sluggish and is expressed in the formation of micro- and nanoparticles of secondary minerals. Under such conditions, the slow diffusion redistribution of uranium with enrichment in absorbed forms relative to all other uranium species is realized as well. The products of secondary alteration of Fe- and Ti-bearing minerals serve as the main sorbents of uranium. The rate of alteration of minerals and conversion of uranium species into absorbed forms is slow, and the results of these processes are insignificant, so that the rocks and uranium species therein may be regarded as unaltered. Under reducing conditions, subsurface water is always saturated with uranium. Whether water interacts with rock or uranium ore, the equilibrium uranium concentration in water is only ≤10^?8 mol/l. Uraninite ore under such conditions always remains stable irrespective of its age. The stability conditions of uranium ore are quite suitable for safe insulation of SNF, which consists of 95% uraninite (UO₂) and is a confinement matrix for all other radionuclides. The disposal of SNF in massifs of crystalline rocks at depths below 500 m, where reducing conditions are predominant, is a reliable guarantee of high SNF stability. Under oxidizing conditions of the upper hydrodynamic zone, the rate of interaction of rocks with subsurface water increases by orders of magnitude and subsurface water is commonly undersaturated with uranium. Uranium absorbed by secondary minerals, particularly by iron hydroxides and leucoxene, is its single stable species under oxidizing conditions. The impact of oxygen-bearing water leads to destruction of uranium ore. This process is realized simultaneously at different hypsometric levels even if the permeability of the medium is variable in both the lateral and vertical directions. As a result, intervals containing uranyl minerals and relics of primary uranium ore are combined in ore-bearing zones with intervals of completely dissolved uranium minerals. A wide halo of elevated uranium contents caused by sorption is always retained at the location of uranium ore entirely destroyed by weathering. Uranium ore commonly finds itself in the aeration zone due to technogenic subsidence of the groundwater table caused by open-pit mining or pumping out of water from underground mines. The capillary and film waters that interact with rocks and ores in this zone are supplemented by free water filtering along fractures when rain falls or snow is thawing. The interaction of uranium ore with capillary water results in oxidation of uraninite, accompanied by loosening of the mineral surface, formation of microfractures, and an increase in solubility with enrichment of capillary water in uranium up to 10^?4 mol/l. Secondary U(VI) minerals, first of all, uranyl hydroxides and silicates, replace uraninite, and uranium undergoes local diffusion redistribution with its sorption by secondary minerals of host rocks. The influx of free water facilitates the complete dissolution of primary and secondary uranium minerals, the removal of uranium at the sites of groundwater discharge, and its redeposition under reducing conditions at a greater depth. It is evident that the conditions of the upper hydrodynamic zone and the aeration zone are unfit for long-term insulation of SNF and high-level wastes because, after the failure of containers, the leakage of radionuclides into the environment becomes inevitable.     

The thermal structure of a shallow lake in early winter

The thermal structure of a shallow lake in the first month of its freeze up is shown to vary widely from year to year. The rate of temperature increase at different horizons of the water mass in early winter is evaluated, and warming of shallow and deep-water areas in the lake are shown to be uneven. The distribution of near-bed temperature as a function of water depth in the first weeks of freeze up features wide variations, though this relationship becomes more regular over time. Estimates of the effective thermal diffusivity are given for different seasons. The main periods in the variations in the heat content of water column in early winter are estimated.     

Diurnal atmospheric forcing and temporal variations of the nutation amplitudes

A 29-year time-series of four-times-daily atmospheric effective angular momentum (EAM) estimates is used to study the atmospheric influence on nutation. The most important atmospheric contributions are found for the prograde annual (77 μas), retrograde annual (53 as), prograde semiannual (45 as), and for the constant offset of the pole (δψsinɛ₀=−86 as, δɛ=77 as). Among them only the prograde semiannual component is driven mostly by the wind term of the EAM function, while in all other cases the pressure term is dominant. These are nonnegligible quantities which should be taken into account in the new theory of nutation. Comparison with the VLBI corrections to the IAU 1980 nutation model taking into account the ocean tide contribution yields good agreement for the prograde annual and semiannual nutations. We also investigated time variability of the atmospheric contribution to the nutation amplitudes by performing the sliding-window least-squares analysis of both the atmospheric excitation and VLBI nutation data. Almost all detected variations of atmospheric origin can be attributed to the pressure term, the biggest being the in-phase annual prograde component (about 30 as) and the retrograde one (as much as 100200 as). These variations, if physical, limit the precision of classical modeling of nutation to the level of 0.1 mas. Comparison with the VLBI data shows significant correlation for the retrograde annual nutation after 1989, while for the prograde annual term there is a high correlation in shape but the size of the atmospherically driven variations is about three times less than deduced from the VLBI data. This discrepancy in size can be attributed either to inaccuracy of the theoretical transfer function or the frequency-dependent ocean response to the pressure variations. Our comparison also yields a considerably better agreement with the VLBI nutation data when using the EAM function without the IB correction for ocean response, which indicates that this correction is not adequate for nearly diurnal variations. Received: 10 September 1997 / Accepted: 5 March 1998     

Rock salt mass in the Paleoproterozoic sequence of the Onega trough in Karelia (from the Onega parametric well data)

A thick (200 m) rock salt mass covering Late Archean granitoids was exposed for the first time in the Early Proterozoic volcanogenic-sedimentary formations in the Onega trough of the east Baltic Shield by the Onega parametric well. The mineral composition of salts, their geochemical features, and the isotopic composition of carbonate carbon and oxygen have been studied. After fluid inclusions present in salts, their metamorphism temperature and isotopic composition of helium and argon were determined. The obtained results give evidence of the fact that rock salts and magnesites associated with them were formed in an evaporate basin with participation of deep crustal processes. The age of the underlying granitoids (2.716 ± 9 Ma) is determined using the Pb—Pb method.