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Том 69, № 1 (2024)

Мұқаба

Бүкіл шығарылым

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Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Articles

Formation of oceanic crust within the Andrew Bain fault zone of the Southwest Indian ridge (Petrological and geochemical data)

Sushchevskya N., Scherbakov V., Peive A., Dubinin E., Belyatsky B., Zhilkina A.

Аннотация

A petrogeochemical study of basalts (lithophile elements and Sr-Nd-Pb isotopes, compositions of liquidus olivine and spinel) from the transition zone of the Southwest Indian Ridge in the area of the Du Toit and Andrew Bain faults revealed significant differences in their composition. Within the rift valley adjacent to the faults, tholeiites enriched in Na and depleted in Fe (Na-TOR genetic type) are typical. Deep-type basalts (TOR-1) are present in the western side of the Andrew Bain Fault. The outpouring of these types of magmas reflects a possible change in geodynamic regime during this zone formation: from deeper and higher temperature melting to shallower ones (Sushchevskaya et al., 2022).

Differences in the primary melts of tholeiites from the rift valley and the Andrew Bain Transform Fault are also traced in the liquidus olivine compositions. The rift valley olivines are similar to typical Na-TOR olivines with a Mg content of Fo88–87, low Ni and elevated Mn. On the contrary, tholeiite olivines of the Andrew Bain Fault are enriched in Ni and depleted in Mn, which may indicate pyroxenite included in the primary melt formation. This component is either oceanic lithosphere recycled through the deep mantle or fragments of previously formed oceanic crust, which are subsequently involved in melting during the spreading axes jumping. A similar process is typical for the region of the Bouvet Triple Junction, where a significant heterogeneity of the olivine composition in terms of trace-element contents was revealed.

The isotope characteristics of the Andrew Bain Fault tholeiites differ in Pb and Sr radiogenic composition and are similar to those of enriched magmas from such Indian Ocean rises as Crozet, Marion and Bouvet, but not from the Konrad and Af. Nikitin Rises. The source of such tholeiite melts is close in composition to the model HIMU type (with high U/Pb), possibly with an admixture of mantle material with EMII characteristics (with elevated Rb/Sr).

Geohimiâ. 2024;69(1):3-20
pages 3-20 views

Major, volatile, ore, and trace elements in magmatic melts from main geodynamic settings. II. Similarity and differences

Naumov V., Girnis A., Dorofeeva V.

Аннотация

Based on the mean contents of elements and their standard deviations estimated in the first part of this research project (Naumov et al, 2022), we compared in detail the distinguished geodynamic settings. In order to compare the compositions of mafic melts, a correction to take into account changes related to the fractionation of main minerals was introduced. The use of numerical criteria made it possible to determine the sequence of elements by the degree of coherence during melting and crystallization of the main magmatic melts. Within this sequence, a regular variation in elemental contents normalized to the average composition of oceanic island melts was established. The melts of mid-ocean ridges show a monotonous increase in normalized contents from the most incompatible (Cs, Ba, U, La, etc.) to compatible elements (Sc, Ni, Cr). The settings of convergent plate boundaries show relative enrichment in the most incompatible elements and significant negative Ta-Nb anomalies relative to neighboring elements. The magmas of continental rifts show the highest enrichment in the most incompatible elements, as well as Pb, Li, and some other elements. Indicator element ratios showing significant variations between the settings were distinguished for mafic melts. Some element ratios are almost identical (within observed variations) in mafic melts from all the settings. The mean element ratios in mafic, intermediate, and silicic magmas show three types of behavior. Some ratios (including the canonic ratios Nb/Ta, Zr/Hf, etc.) in intermediate and silicic magmas are inherited from the composition of mafic melts. Some ratios show irregular changes from mafic to silicic melts (Sr/Cr, F/Th, etc.). There are ratios that changes monotonously and significantly in the sequence from mafic to silicic melts (Ni/Yb, Lu/P, etc.). The variations of element ratios are related to the crystallization differentiation of melts and contributions of geochemically contrasting reservoirs.

Geohimiâ. 2024;69(1):21-35
pages 21-35 views

Peritectic reaction of olivine in the diamond-forming system carbonate-silicate-(C-O-H) at 6 GPa

Kuzyura A., Spivak A., Litvin Y.

Аннотация

Influence of the supercritical C-O-H-fluid (7.5 wt.%) onto melting phase relations of the multicomponent multiphase diamond-forming system olivine-jadeite-diopside-(Mg-Fe-Ca-Na-carbonates)-(C-O-H) in experiments at 6 GPa and 700–1200 °C (the upper mantle conditions) has been studied. The peritectic reaction of olivine and jadeite-bearing melt with garnet formation has been retained as a key mechanism of the ultrabasic-basic evolution of diamond-forming melts. The CO2-fluid and silicate components react forming carbonate phases. The H2O-fluid together with carbonates has essentially lowered temperatures of the liquidus and solidus boundaries. The phase of supercritical water fluid and water-bearing carbonate nesquehonite (Nes) MgCO3·3H2O were identified with the Raman-spectroscopy method after crystallization of the completely mixed silicate-carbonate-(C-O-H-fluid) melt.

Geohimiâ. 2024;69(1):36-50
pages 36-50 views

High precision determination of carbon isotope composition and concentration of dissolved inorganic carbon in seawaters

Dubinina E., Kossova S., Chizhova Y.

Аннотация

Determination of the isotopic composition and concentration of dissolved inorganic carbon (DIC) in sea water requires not only high measurement accuracy, but also the development of unified approaches to data standardization and material collection. In this work, we studied the effect of sampling methods (“in a container” and “in a vial with acid”, with and without the toxin) on the results of determining the values of δ13C(DIC) and the concentration of DIC in sea water. The analytical protocol was described in detail, based on many years of experience in the selection, measurement and standardization of data obtained for a large number of water samples of the Arctic seas. According to this protocol, the values of δ13C(DIC) and [DIC] can be determined with an error of less than 0.05 ‰ (1σ) and 4.5 rel.% respectively. It has been shown that sampling “in a vial with acid” with their storage for 4 months is accompanied by significant contamination by atmospheric carbon dioxide with an underestimation of δ13C(DIC) values by an average of 0.3–0.8 ‰ and an overestimation of [DIC] values by an average of two times. The absence of the toxin that stops biological activity does not lead to significant shifts in the DIC concentration, but it strongly affects the δ13C(DIC) values, which become underestimated by an average of 1 ‰. Using sampling “in a container”, with toxin addition, and following other recommendations, the samples retain the isotope and concentration parameters of DIC for at least year.

Geohimiâ. 2024;69(1):51-62
pages 51-62 views

Provenance changes of the holocene deposits of Oga and Tsivolki bays (Novaya Zemlya archipelago) according to SR, ND, PB isotope data

Vishnevskaya I., Kostitsyn Y., Okuneva T., Soloshenko N.

Аннотация

The paper is devoted to the Sr-, Nd-, Pb-isotope data obtained for two cores of bottom sediments taken in the Oga and Tsivolki bays of the Severny Island of the Novaya Zemlya archipelago. The studied sequence of sediments from Oga Bay has been accumulated over the last thousand years. The 87Sr/86Sr ratio decreases from top to bottom down the section from 0.72225 to 0.71995, the value of εNd varies from –6.1 to –5.5. The Pb isotopic composition varies within narrow limits: the 206Pb/204Pb ratio from 19.107 to 19.139, the 207Pb/204Pb ratio from 15.632 to 15.635, and the 208Pb/204Pb ratio from 38.568 to 38.635. A rapid decrease in the 87Sr/86Sr ratio at a relatively stable neodymium and lead isotope composition indicates a change in the source of the clastogenic material. This can be explained by the fact that the material of the destruction of Permian clay shales, and then the Devonian-Silurian sedimentary carbonates, first entered the area of glacier abrasion and further, respectively, into the sedimentation zone.

The sediment column from the Tsivolki Bay was formed over a little more than 10 thousand years. Based on the Sr, Nd, and Pb isotope ratios, these bottom sediments are divided into lower and upper parts: before and after 150 cm (or ~3500 years). In the lower part of the column, the 87Sr/86Sr ratio increases from 0.72055 to 0.72580, the value of εNd remains approximately the same and varies around –8.2. In the upper part, the 87Sr/86Sr ratio drops to 0.72049 in the near-surface layer; at the same time, the value of εNd increases to –6.4. At the boundary of these two units, the 206Pb/204Pb ratio abruptly changes from about 18.0 in the lower part to 19.3 in the upper part and 208Pb/204Pb from about 36.5 in the lower part to 38.7 in the upper part of the section. The change in the Sr, Nd, and Pb isotope characteristics is likely a reflection of changes in the composition of the rocks in the area where the basin was removed, which is now being eroded by the glacier.

Comparison with modern sources supplying clastic material to the Kara Sea showed that the material inputs the Oga and Tsivolki bays only from Novaya Zemlya.

Geohimiâ. 2024;69(1):63-76
pages 63-76 views

The role of biochemical processes in formation of waters and bottom sediments after reduction of anthropogenic pollution

Moiseenko T., Leummens E.

Аннотация

The article is devoted to anthropogenic and biogeochemical processes that affect the water and bottom sediment (BS) formation of the subarctic Lake Imandra. The data of long-term observations were presented, showing changes in the water chemical composition during the period of maximum pollution and after decrease in anthropogenic load within the last 30 years. It was found that the content of toxic metals in water decreased, but due to climate warming, the input of organic matter and nutrients increased, which stimulated an increase in the intensity of production processes. Enrichment of water during the period of intensive heavy metal pollution led to their accumulation in bottom sediments (BS); the highest metal concentrations detected in the surface layers, which belong to the modern period of sedimentation. The development of oxygen-free conditions in bottom horizons due to sedimentation and oxidation of organic matter, which leads to metal cycling that prevents their burial was shown. Physicochemical and biogeochemical processes are considered as explaining the diffusion of metals to the surface of bottom sediments and the formation anomalously high concentrations of metals in the surface layers of BS. The hypothesis of the appearance of the diagenesis initial stage in bottom sediments was proposed.

Geohimiâ. 2024;69(1):77-90
pages 77-90 views

Geochemical features of deluvial-lacustrine sedimentogenesis in the basin of lake Chistoye, Northern Priokhotsk area

Minyuk P., Pozhidaeva D., Sotskaya O., Burnatny S.

Аннотация

The results of the geochemical study of loose sediments of the catchment basin and bottom sediments of Lake Chistoye, located in the Northern Priokhotye, showed that the lake was formed at the beginning of the early Holocene about 11200 cal. years ago. Terrigenous sedimentation dominates in it, i. e. the geochemical characteristics of sediments are determined by the particle sizes. Thin grain size sediments have low SiO2, Na2O, K2O, CaO, and Sr contents; and are enriched with Al2O3, TiO2, MgO, Fe2O3, and V. Changes in the nature of sedimentation may be due to climatic reasons and may be associated with cold Bond events. In the Early Holocene, mostly thin silts were deposited in Lake Chistoye. The impulse of “coarse-grained” sediments (>140 microns) enriched with silica occurred (9760–9650) and 8810 cal. years ago. A noticeable accumulation of relatively coarse-grained sediments occurred at the very beginning of the Middle Holocene 8540–6920 cal. years ago, as well as 6140 and 4450 cal. years ago. For the Late Holocene, the input of detrital material with increased SiO2 contents was noted in the range of 3470–850 cal. years ago.

Geohimiâ. 2024;69(1):91-112
pages 91-112 views

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