


Vol 57, No 2 (2019)
- Year: 2019
- Articles: 8
- URL: https://journals.rcsi.science/0016-7029/issue/view/9456
Article
Long-Lasting Influence of the Discovery Plume on Tholeiitic Magmatism in the South Atlantic: Data on Basalts Recovered by Hole 513a, DSDP Leg 71
Abstract
The paper presents the very first data on concentrations of major and trace elements; Sr, Nd, and Pb isotopic ratios of rocks; and the composition of olivine phenocrysts of 38-Ma basalts recovered by Hole 513a (DSDP Leg 71) in the South Atlantic. The bulk-rock samples and the chilled glasses are mildly magnesian (7–8 wt % MgO) and bear elevated FeO and low Na2O concentrations, as is typical of MORB of the TOR-1 type. Olivine phenocrysts (Fo84.5–88) in these rocks contain concentrations of trace elements (Ni, Mn, Cr, and Zn) that are typical of classic MORB, which are produced by partial melting of mantle peridotite. The rocks are strongly depleted in incompatible elements [(La/Sm)n ~ 0.6] but have elevated Ba/Nb, K/Nb, and Pb/Ce ratios and Cu, Ag, and Au concentrations that are 1.5–4 times higher than in typical depleted MORB (N-MORB) and in most rift basalts in the South Atlantic. Isotope compositions of the basalts (average ratios 206Pb/204Pb ~ 18.0; 207Pb/204Pb ~ 15.6, 208Pb/204Pb ~ 38.0, 143Nd/144Nd ~ 0.5130, and 87Sr/86Sr ~ 0.7040) are close to those in modern tholeiites from the southern MAR segment (SMAR) north of the Agulhas Fracture Zone. The data indicate that the magmas were derived from a strongly depleted mantle source that contained a minor (~3%) admixture of an enriched component, which is discernible in the magmas of the Discovery hotspot. The composition of the source, which is more depleted than DM, and the high degrees of melting of this source explain why the basalts from DSDP Hole 513a are enriched in chalcophile elements. It is believed that spreading magmatism at 45°–48° S in SMAR as far back as 40 Ma was already affected by the Discovery hotspot. This hotspot might be related to the Tristan plume system, and its origin and long-lasting influence on spreading magmatism in the South Atlantic are regarded as evidence of the extensive effect of the Tristan plume.



Genesis of Diamonds and Paragenetic Inclusions under Lower Mantle Conditions: The Liquidus Structure of the Parental System at 26 GPa
Abstract
The regularities of the joint genesis of diamonds and their paragenetic inclusions under lower mantle conditions are controlled by the melting relations at the liquidus of the multicomponent diamond-forming system. The boundary compositions of this system are evident from the generalized data on the analytical mineralogy of paragenetic inclusions in lower-mantle diamonds. The structure of the liquidus of the diamond-forming system was studied in a physicochemical experiment for P–T parameters typical of the depths of 670–800 km. The compositions of parental melts/solutions for diamonds and paragenetic inclusions correspond to the multicomponent system MgO–FeO–СаО–SiO2–MgCO3–FeCO3–CaCO3–Na2CO3–C. Its primary melting is controlled by the peritectic phase relations at the solidus, which was shown as a result of experimental studies of polythermal sections of the system during a study of their phase diagrams. Of key importance is the effect of the “stishovite paradox,” i.e., the peritectic reaction between the ultrabasic bridgmanite phase and melt with the formation of basic oxide associations of periclase–wustite solid solutions and stishovite. The peritectic reaction of bridgmanite is a fundamental feature of the diamond-forming system and determines the major peculiarity in its liquidus structure. Structure of the peritectic liquidus provides the physicochemical basis for the evolution of growth melts of diamonds and their paragenetic minerals. Based on the experimental data, we have constructed a fractional diagram of syngenesis of diamonds and inclusions clearly illustrating the solution–melt mechanism of diamond genesis and sequence of growth trapping of primary inclusions by diamonds under the lower-mantle conditions. The physicochemical factors of the genesis of diamonds and primary inclusions are agreed and generalized in a compositional diagram of lower-mantle diamond-forming media, and they provide a natural basis for the genetic classification of inclusions of rock-forming and accessory minerals in diamonds



Tendencies of REE Distribution in the Kivakka Olivinite–Gabbronorite Layered Intrusion (Northern Karelia)
Abstract
Abstract—This work is devoted to the examination of REE behavior in rocks of the Kivakka olivinite–gabbronorite layered intrusion (Northern Karelia). The paper reports detailed petrographic characteristics of mineral assemblages throughout the massif section. It is shown that the same minerals are present as both intercumulus and cumulus phases depending on the degree of melt fractionation. Their contents which determine the petrographic characteristics and rock name are not indicative of their presence in cumulate assemblage (cumulus phase). REE contents in rocks and rock-forming minerals are analyzed, including their variations in the vertical section as well as in the critical zones of contrasting intercalation. REE in the Kivakka massif behave as incompatible elements, are accumulated in a residual melt together with U, Th, Zr, and other incompatible elements, and can be used as indicator of the degree of melt fractionation. In some cases, they could reflect different structural–genetic features such as the cumulus density in the similar cumulus assemblages. Hydrothermal alteration strongly affects the Ce content. The similar shape of REE patterns indicates the close-system crystallization differentiation of the massif.



Origin of Skarns at Migmatization on Ol’khon Island, Lake Baikal, Russia
Abstract
Migmatites on the western shore of Ol’khon Island host unusual rocks: zoned lenses of hedenbergite–garnet–epidote–anorthite metasomatites coupled with the migmatites. No intrusive granites were found nearby. The skarn-forming process operated at the interface of the granite gneiss and skarn protolith (perhaps, carbonate rocks). The composition of the metasomatites is analogous to that of calcic skarns with high Al2O3, FeO, and CaO concentrations. The compositions and relations of the minerals provide evidence of the successive development of the hedenbergite–anorthite outer zone, dominantly anorthite–garnet main zone, and quartz-enriched inner zone, with all of the zones parallel to contact with the granite gneiss. The granite gneiss itself is also likely of metasomatic nature, as follows from its supraeutectic concentration of potassic feldspar in the leucosome and low crystallization temperatures. A minimum of the Gibbs free energy (calculated with the SELECTOR-C program package) was reached at 8 kbar and temperatures of 600–625°C. These parameters are lower than the melting temperature of the granite eutectic, and the absence of melt is confirmed by the absence of melt inclusions in minerals of the granite gneisses. This indicate that the driving force of the process was migmatizing silicic–potassic solutions. The P–T parameters of the skarns are close to the foregoing values. The very high Sr and Ca and low Mg concentrations suggest that the protolith of the skarns was calcite marble. The enrichment of the skarns in the granitophile elements suggests that the skarns were produced simultaneously with and in genetic relation to the migmatization processes. The metasomatites were formed before the partial melts were derived, early in the course of the granite-forming processes and provide important information for better understanding the metasomatic process responsible for the exchange of chemical elements between the rocks.



Authigenic Titanium and Zirconium Minerals at the Verkhnekamskoe Salt Deposit
Abstract
The salt-bearing and suprasalt units at the Verkhnekamskoe salt deposit contain newly formed Ti oxides and zircon. The minerals may have been produced at the decomposition of clay material and release of colloid Ti and Zr hydroxides during diagenesis, catagenesis, and supergenesis because of sulfate reduction and an acidic environment caused by Fe2+ oxidation in the sylvite and carnallite. Anatase was found in both the suprasalt units and the salt-bearing ones, whereas rutile occurs exclusively in the bottom part of the salt-bearing unit. The possible reasons for this distribution may have been intensification of the catagenetic transformations with depth and the composition of the coexisting sulfate or chloride brines, respectively. The anatase typically forms pinacoidal crystals, which give way to dipyramidal ones in the carnallite zone (whose solutions are the most acidic). The rutile shows twins of three types, whose origin was caused by the growth of the mineral in the fine-grained material of dehydrated Ti hydroxide colloid. The Ti oxides contain V, Cr, Zr, and (Al, Si, and Fe) admixtures, which reflect the geochemistry of the erosion regions which provided the aluminosilicate material.



Geochemistry of Suspended Matter in the Amazon River Waters
Abstract
Abstract—The duplicate samples of the Amazon River suspended matter (SM) collected during the 9th cruise of R/V Professor Shtokman were studied using modern analytical techniques. Waters of the Amazon basin are subdivided into three main types differing in SM content and chemical composition: white (turbid yellow waters of the Amazon River and Madeira tributary), clear (transparent waters of the large Xingu, Tapajós, Trombetas, and Tocantins tributaries) and black (waters with strong coffee color, high content of dissolved organics, and elevated acidity, Riu Negro). The specific features of SM from different parts of the river basin have been established. The contents and relationships of major and trace elements in the SM vary within wide ranges, but in general the bulk composition of the SM is close to the average composition of river SM and clay rocks, except for some samples from clear waters. The SM of the white and clear waters (blackwater samples unfortunately have not been preserved) are enriched in mercury. Literature data indicate that artisanal gold mining with the use of mercury (amalgamation method) has been carried out for many years in the Amazon Basin, i.e., the SM enrichment in mercury is related to the anthropogenic factor. At the same time, significant (up to two orders of magnitude) enrichment of SM of the clear water Xingu and Tokantins rivers, the Amazon tributaries, in tin, zink, lead, and to lesser extent, in copper, cadmium, silver, and some other metals give grounds to suggest ore mineralization in these regions.



Division and Correlation of the Upper-Middle Cambrian Evaporate Platform Facies Dolomite Formation in Tarim Basin
Abstract
The Cambrian strata in Tarim basin is mainly evaporate platform facies dolomite. Due to the lack of trilobite fossils, it is hardly to achieve isochronous stratigraphic division and correlation. The Xiaoerbulake outcrop and Fang 1 well are typical surface and subsurface Cambrian sections in Tarim Basin respectively. Shayilike, Awatage and Xiaqiulitage Groups were regarded as the complete Upper -Middle Cambrian previously which composed of dolomite. The carbon isotope values range from –15.5 to 2‰, and three negative excursions are found (N1, N2 and N3). Comparing with the Global Standard Chronostratigraphic Scale for the Middle and Upper Cambrian System, the fifth stage and the Drumian of the third Series, the ninth and the tenth Stage of Furongian Series can be recognized, while the Guzhangian and Paibian are lost. As a result, the Cambrian Formation in Tarim Basin can be divided accurate to stage scale.



Short Communications
Diagenesis of Organic Matter in Peat: Rock–Eval Pyrolysis Data
Abstract
Rock–Eval pyrolysis data were obtained on a collection of peat samples at various diagenesis stages (from depths of 0–350 cm) from the Gurskoe deposit, lower Amur area, and on producers of organic matter (OM). The pyrograms of the peat OM are superpositions of three peaks: (1) a low-temperature one, with temperatures of hydrocarbon release lower than 300°C, (2) an intermediate-temperature peak, with hydrocarbons released at 300–400°C, and (3) a high-temperature one, corresponding to hydrocarbon release at temperatures above 400°C. The peaks correspond to the lipid, labile, and kerogen OM components, respectively. The diagenetic transformation of OM is associated with a gradual decrease in the contents of the lipid and labile components and an increase in the content of the kerogen component. The process is the most intense in the upper part of the vertical section.


