Geology and petrology of the lava complex of Young Shiveluch Volcano, Kamchatka

Detailed geological and petrological-geochemical study of rocks of the lava complex of Young Shiveluch volcano made it possible to evaluate the lava volumes, the relative sequence in which the volcanic edifice was formed, and the minimum age of the onset of eruptive activity. The lavas of Young Shiveluch are predominantly magnesian andesites and basaltic andesites of a mildly potassic calc-alkaline series (SiO₂ = 55.0–63.5 wt %, Mg# = 55.5–68.9). Geologic relations and data on the mineralogy and geochemistry of rocks composing the lava complex led us to conclude that the magnesian andesites of Young Shiveluch volcano are of hybrid genesis and are a mixture of silicic derivatives and a highly magnesian magma that was periodically replenished in the shallow-depth magmatic chamber. The fractional crystallization of plagioclase and hornblende at the incomplete segregation of plagioclase crystals from the fractionating magmas resulted in adakitic geochemical parameters (Sr/Y = 50–71, Y < 18 ppm) of the most evolved rock varieties. Our results explain the genesis of the rock series of Young Shiveluch volcano without invoking a model of the melting of the subducting Pacific slab at its edge.     

The nature of scattered and concretion pyrite in the Upper Abalak Formation of the Salym oil field (Western Siberia)

Dispersed and concretionary pyrite in chert–clay–carbonate and carbonate rocks of the Abalak Formation (Salym oil field) have been studied. The study was conducted using Scanning Electron Microscopy (SEM), Electron Probe Microanalysis (EPMA), and high spatial resolution Secondary Ion Mass Spectrometry (Nano-SIMS). As a result, three morphological groups of pyrite have been distinguished: large cubic crystals, framboidal pyrite, and fine-crystal aggregates that replace organic remnants. The sulphur isotope ratio allows one to distinguish two genetic types of pyrite. The source of the sulphur for the first genetic group was H₂S produced by bacterial sulphate reduction, while the second group pyrite was formed with sulphur as a product of thermochemical sulphate reduction.     

Mesozoic age of granitoids from the Beket complex (Gonzha block within the Argun terrane of the Central-Asian Fold Belt)

U-Pb geochronological results confirm the Mesozoic age (124 ± 1 Ma) of the Beket granitoid complex, previously interpreted as being one of the markers amongst the Early Proterozoic magmatic complexes within the Amur superterrane (microcontinent) of the Central Asian Fold Belt. This implies that the structural and metamorphic amphibolite facies overprints documented either in the Beket granitoids or Gonzha host rocks are evidently Mesozoic rather than Early Proterozoic in age.     

Authigenic zeolites in the sedimentary mantle of the world ocean

The paper deals with results of general and systematic analysis of data from deep-sea drilling (360 stations) and a personal study carried out by the authors on the distribution and facies location of authigenic zeolites in the sedimentary mantle of the World Ocean.The scheme of zeolite distribution, compiled for the Holocene—Pleistocene, Miocene, Eocene and Cretaceous periods confirmed the previously established global stratification of zeolites. It showed that the main mass of phillipsite was formed during the Pleistocene—Holocene, while clinoptilolite was a predominant mineral in Eocene and Cretaceous rocks. Both zeolites were wide-spread in the Oligocene and Miocene. Facies location and paragenesis of associated minerals as well as the original material of their formation are different for phillipsite and clinoptilolite.The most probable reasons for vertical stratification of oceanic zeolites of global significance are changes of the character of volcanism in time and general evolution of sedimentation in the World Ocean.     

Rare earth elements in the clay fraction of coaliferous sediments of the Arkagalinskoe (Magadan district) and Dolinskoe (Sakhalin Island) coalfields

The study of REE distribution in the clay fraction of sedimentary rocks from two coalfields made it possible to distinguish several types of REE distribution, which correlate with their mineral composition. It is shown that the REE fractionation was related to the mineral reconstruction of the primary clay fraction and some detrital minerals in the course of postsedimentary transformations of rocks during diagenesis, early catagenesis, and beginning of late catagenesis. These transformations were governed by several factors, such as the composition of sediments; hydrochemical features of accumulation environment; the chemical composition, dynamics, and feeding sources of pore solutions; the porosity and permeability of sediments and rocks; and the content of organic matter and its reaction ability.     

An Experimental Determination of Iron Biotite-Alkali Feldspar Equilibria

Experiments in the system KAlSi0₄-NaAlSi0₄-SiOj-Fe-0-H indicatethat approximately 20 mole per cent of sodium annite [NaFe₃AlSiO₁₀(OH)₂]can enter into solid solution with potassium annite. This substitutionreduces the biotite stability field. With excess alkali feldsparand no free quartz, the following reactions limit the biotitestability: Feldspar(s)+biotite feldspar(s)+magnetite+vapor. (1) Feldspar+biotite feldspar+fayalite+leucite+vapor. (2) Feldspar+biotite feldspar+fayalite+liquid+vapor. (3) Biotite feldspar+fayalite+nepheline+vapor. (4) On the QFM buffer (P_Total = 2 Kb), reaction 1 occurs at 685°C in the sodium free system and at 625 °C when twofeldspars are present; on NNO, it occurs at 630 and 590 °C.On the G-CH buffer, reaction 2 is stable at high temperatures(795–830 °Q and potassic compositions (), reaction3 at intermediate conditions (T = 740–95 °C; ) andreaction 4 at lower temperatures (710–40 °C) and sodiccompositions (). In the presence of excess quartz, reaction1 remains stable below the QFM buffer, but the reaction Feldspars)+biotite+quartz feldspars)+fayalite+vapor (5) is stable at higher hydrogenfugacities. On the G-CH buffer, reaction 5 occurs at 610 °Cin the sodium free system and at 595 °C when two alkalifeldspars are present. On the MW buffer, the temperatures are585 and 515 °C (M.I.). The experimental data presented suggest that biotite will notbe stable in the presence of granitic liquids at total pressuresbelow 4 kb, providing the fluorine and titanium content of thebiotite is low. They also suggest that gradients in the a£1S,l0 in a rock could produce variations in the biotite Fe/Fe+Mgratio and in extreme cases could result in the complete breakdown(decreased ) of biotite or its crystallization (increased )where previously there was none.     

Geochemical types of Volkhovites and possible diamond resource potential of areas occupied by Holocene fluidisites

Volkhovites—tektite-like glasses—have been detected in the Holocene glacial drift along the right bank of the Volkhov River. A cryptomagmatic model of their formation and pre-Holocene age of volkhovite melts, cinder, and frothed glasses has been suggested (Skublov et al., 2007). Four geochemical types of volkhovites are distinguished: (1) manganous (Mn, Fe, Cr, V, Si, Nb, Pb, H), (2) magnesian (Mg, Al, Ti, F, B), (3) potassic (K, Rb, Cs), and (4) calcic (Ca, REEs, Ba, U, Th, Ta, Hf, Y, Sc, Cl). In light of the geochemical data, volkhovites are regarded as natural silicate glasses of kimberlite-carbonatite composition. Their types are called kimberlitic (Mn type), kimberlitic-carbonatitic (Mg type), lamproitic-carbonatitic (K type), and carbonatitic (Ca type). Volkhovites are suggested to be indicators of undiscovered diamond mineralization of kimberlite or carbonatite (Chagatai) types.     

Stability of a stationary Rossby wave embedded in barotropic monsoon zonal flow

Barotropic stability of a stationary Rossby wave of wavelength 30° longitude superposed on the uniform monsoon zonal flow has been examined. The wave is unstable to perturbations and the growth rate depends on the meridional scale. These perturbations grow by drawing on the kinetic energy of the stationary Rossby wave.     

Copper(II) humate mobility in kaolinite soil

An investigation of the influence of humate on the mobility of copper(II) ions in a kaolinite soil using leaching tests and electrokinetic experiments is reported. The data are interpreted in terms of humate–copper–clay interactions and humate electrical charge. Humate is mostly immobile below pH8 but is more mobile in alkaline conditions (sorption to kaolinite reduces its mobility in neutral conditions). Copper humate complexes are mobile in both acidic and alkaline conditions, but not in neutral conditions where they are sorbed. The dissolved copper humate complexes that form in acidic conditions are positively charged. The net effect of humate is to increase cupric ion mobility in kaolinite soil, especially in alkaline conditions.     

Geochemistry and geochronology of proterozoic tholeiite dykes of east antarctica: evidence for mantle metasomatism

Two episodes of tholeiite dyke emplacement have been identified in Archaean high-grade metamorphics of the Napier Complex in Enderby Land. Middle Proterozoic Amundsen dykes are typical continental tholeiites and most of the chemical variation in individual suites can be explained in terms of different degrees of partial melting and low-pressure crystal fractionation. Group I Amundsen tholeiites were derived from a relatively homogeneous source region 1,190±200 m.y. ago, whereas that of the group II Amundsen tholeiites was chemically and isotopically heterogeneous. Group II dykes have various degrees of enrichment in incompatible elements, and commonly show normalised trace element abundance patterns with negative Nb anomalies. These features imply variable metasomatism of the source region by a volatile-rich fluid phase (rather than a melt of any observed igneous composition) enriched in K, Rb, Ba, Th, and possibly La and Ce.Early Proterozoic (2,350±48 m.y.) tholeiites were emplaced at considerable depths in the crust during the waning stages of granulite-facies metamorphism and include a high-Mg suite of possible komatiitic affinity, ranging in composition from hypersthene-rich tholeiite (norite) to quartz-rich tholeiite. They tend to have higher ratios of highly to moderately incompatible elements (e.g., K/Zr, K/Ce), and larger Nb anomalies (i.e., higher K/Nb) compared with middle Proterozoic tholeiites, suggesting derivation from more enriched source regions. Isotopic data are not compatible with significant crustal contamination, but constrain source metasomatism to a time immediately before emplacement. Metasomatism of the source region of the much younger group I tholeiites may have been contemporaneous with that of the high-Mg suite.