Internal deformation of Sikhote Alin volcanic belt, far eastern Russia: Paleocene paleomagnetic results     

Yo-ichiro Otofuji  Takaaki Matsuda  Ryo Enami  Koji Uno  Katsuhiko Nishihama  Li Su  Ruslan G. Kulinich  Petr S. Zimin  Anatoly P. Matunin  Vladimir G. Sakhno 《Tectonophysics》2002,350(3)

We present paleomagnetic results of Paleocene welded tuffs of the 53–50 Ma Bogopol Group from the northern region (46°N, 137°E) of the Sikhote Alin volcanic belt. Characteristic paleomagnetic directions with high unblocking temperature components above 560 °C were isolated from all the sites. A tilt-corrected mean paleomagnetic direction from the northern region is D=345.8°, I=49.9°, α₉₅=14.6° (N=9). The reliability of the magnetization is ascertained through the presence of normal and reversed polarities. The mean paleomagnetic direction from the northern region of the Sikhote Alin volcanic belt reflects a counterclockwise rotation of 29° from the Paleocene mean paleomagnetic direction expected from its southern region. The counterclockwise rotation of 25° is suggested from the paleomagnetic data of the Kisin Group that underlies the Bogopol Group. These results establish that internal tectonic deformation occurred within the Sikhote Alin volcanic belt over the past 50 Ma. The northern region from 44.6° to 46.0°N in the Sikhote Alin volcanic belt was subjected to counterclockwise rotational motion through 29±17° with respect to the southern region. The tectonic rotation of the northern region is ascribable to relative motion between the Zhuravlevka terrane and the Olginsk–Taukhinsk terranes that compose the basements of the Sikhote Alin volcanic belt.  相似文献   

Crystal chemistry of titanite-structured compounds: the CaTi1-x Zr x OSiO4 (x≤0.5) series     

Ruslan P. Liferovich  Roger H. Mitchell 《Physics and Chemistry of Minerals》2005,32(1):40-51

Inhomogeneous aggregates of late-stage titanite enriched in Zr have been described recently from post-magmatic parageneses in silica-undersaturated rocks. In the natural samples, simple isovalent substitution of the large Zr (^[vi]R⁴⁺=0.72 Å) for Ti (^[vi]R⁴⁺=0.605 Å) is limited to an empirical maximum of 0.25 afu (15.3 wt.% ZrO₂). As the natural material is not suitable for crystallographic study, a series of CaTi_1-xZr_xOSiO₄ titanite samples have been synthesized by standard ceramic methods at ambient pressure in air, and their crystal structure determined by Rietveld refinement of laboratory powder X-ray diffraction patterns. All of the synthetic Zr-doped titanite varieties adopt space group A2/a and consist of distorted CaO₇ polyhedra together with less distorted (Ti_1-xZr_x)O₆ octahedra and SiO₄ tetrahedra. Cell dimensions and atomic coordinates together with volumes and distortion indices are given for all polyhedra. The empirical limit for Zr substitution in synthetic (F,OH)-free titanite is 0.5 afu (29.6 wt.% ZrO₂). The existence of a Zr analogue of titanite in nature is considered to be unlikely.  相似文献   

Micro‐PIXE Geochemical Fingerprinting of Nephrite Neolithic Artifacts from Southwest Bulgaria     

Ruslan I. Kostov  Christo Protochristov  Chavdar Stoyanov  Lszl Csedreki  Alíz Simon  Zita Szikszai  Imre Uzonyi  Bisserka Gaydarska  John Chapman 《Geoarchaeology》2012,27(5):457-469

Neolithic artifacts made of nephrite, □Ca₂(Fe,Mg)₅Si₈O₂₂(OH)_2, are found at prehistoric settlements in Bulgaria. This study investigates these objects based on particle induced X‐ray emission using a scanning nuclear microprobe (micro‐PIXE technique). Seven nephrite artifacts from the Neolithic sites of Kovachevo, Bulgarchevo and Galabnik in southwest Bulgaria were analyzed to quantify their composition and to establish if a correlation exists between the distribution of major and trace elements, color, impurities, and texture. The nephrite artifacts are tremolite in composition, with a proposed ultrabasic origin. Based on the geochemical data obtained by micro‐PIXE, we divide the artifacts into Group 1 objects from the Kovachevo site and Group 2 objects from the Galabnik and Bulgarchevo sites. The analytical data and microprobe analyses are compared with geochemical data of nephrite from across the globe. The results are in a good agreement with previous electron microprobe and electron paramagnetic resonance (EPR) spectroscopy data. Our study provides a better understanding of the mineralogy and geochemistry of nephrite artifacts and helps to address questions regarding origin and the distribution of such materials in Bulgaria and other Balkan countries.  相似文献   

Crystallization of melilite from CMAS-liquids and the formation of the melilite mantle of Type B1 CAIs: Experimental simulations     

Ruslan A. Mendybaev  Frank M. Richter  Andrew M. Davis 《Geochimica et cosmochimica acta》2006,70(10):2622-2642

Type B CAIs are subdivided into B1s, with well-developed melilite mantles, and B2s, with randomly distributed melilite. Despite intensive study, the origin of the characteristic melilite mantle of the B1s remains unclear. Recently, we proposed that formation of the melilite mantle is caused by depletion of the droplet surface in volatile magnesium and silicon due to higher evaporation rates of volatile species compared to their slow diffusion rates in the melt, thus making possible crystallization of melilite at the edge of the CAI first, followed by its crystallization in the central parts at lower temperatures. Here, we present the results of an experimental study that aimed to reproduce the texture observed in natural Type B CAIs. First, we experimentally determined crystallization temperatures of melilite for three melt compositions, which, combined with literature data, allowed us to find a simple relationship between the melt composition, crystallization temperature, and composition of first crystallizing melilite. Second, we conducted a series of evaporation and cooling experiments exposing CAI-like melts to gas mixtures with different oxygen fugacities (f_O2). Cooling of the molten droplets in gases with logf_O2?IW-4 resulted in crystallization of randomly distributed melilite, while under more reducing conditions, melilite mantles have been formed. Chemical profiles through samples quenched right before melilite started to crystallize showed no chemical gradients in samples exposed to relatively oxidizing gases (logf_O2?IW-4), while the near-surface parts of the samples exposed to very reducing gases (logf_O2?IW-7) were depleted in volatile MgO and SiO₂, and enriched in refractory Al₂O₃. Using these experimental results and the fact that the evaporation rate of magnesium and silicon from CAI-like melts is proportional to , we estimate that Type B1 CAIs could be formed by evaporation of a partially molten precursor in a gas of solar composition with . Type B2 CAIs could form by slower evaporation of the same precursors in the same gas with .  相似文献   

Kinetic isotopic fractionation during diffusion of ionic species in water     

Frank M. Richter  Ruslan A. Mendybaev  Ian D. Hutcheon  Neil C. Sturchio 《Geochimica et cosmochimica acta》2006,70(2):277-289

Experiments specifically designed to measure the ratio of the diffusivities of ions dissolved in water were used to determine . The measured ratio of the diffusion coefficients for Li and K in water (D_Li/D_K = 0.6) is in good agreement with published data, providing evidence that the experimental design being used resolves the relative mobility of ions with adequate precision to also be used for determining the fractionation of isotopes by diffusion in water. In the case of Li, we found measurable isotopic fractionation associated with the diffusion of dissolved LiCl (D_⁷Li/D_⁶Li=0.99772±0.00026). This difference in the diffusion coefficient of ⁷Li compared to ⁶Li is significantly less than that reported in an earlier study, a difference we attribute to the fact that in the earlier study Li diffused through a membrane separating the water reservoirs. Our experiments involving Mg diffusing in water found no measurable isotopic fractionation (D_²⁵Mg/D_²⁴Mg=1.00003±0.00006). Cl isotopes were fractionated during diffusion in water (D_³⁷Cl/D_³⁵Cl=0.99857±0.00080) whether or not the co-diffuser (Li or Mg) was isotopically fractionated. The isotopic fractionation associated with the diffusion of ions in water is much smaller than values we found previously for the isotopic fractionation of Li and Ca isotopes by diffusion in molten silicate liquids. A major distinction between water and silicate liquids is that water surrounds dissolved ions with hydration shells, which very likely play an important but still poorly understood role in limiting the isotopic fractionation associated with diffusion.  相似文献   

Rhombohedral ilmenite group nickel titanates with Zn, Mg, and Mn: synthesis and crystal structures     

Ruslan P. Liferovich  Roger H. Mitchell 《Physics and Chemistry of Minerals》2005,32(5-6):442-449

Binary, ternary, and quaternary rhombohedral ordered titanates, Ni_1/2Mn_1/2TiO₃, Ni_1/2Mg_1/2TiO₃, Ni_1/3Zn_1/3Mg_1/3TiO₃, and Ni_1/4Zn_1/4Mg_1/4Mn_1/4TiO₃, were obtained by solid-state synthesis at 1095°C at ambient pressure in a nitrogen atmosphere. All of the compounds adopt ATiO₃ (A = Ni, Mn, Zn, and Mg) stoichiometry. Crystal structures were refined by the Rietveld method from powder X-ray diffraction data. Unit cell parameters and unit cell volumes decrease with decreasing average radius of the ^vi A ²⁺ cation. All the synthetic titanates adopt the space group and the ilmenite structure consisting of distorted AO₆ and TiO₆ octahedra. The divalent cations and Ti⁴⁺ are distributed in layers of octahedra alternating along c with no evidence for disorder. In common with pyrophanite, NiTiO₃, and ilmenite sensu stricto, the distortion of the AO₆ octahedra is less than that of the TiO₆ octahedra. The Ti⁴⁺ and A-site cations in the titanates are off-centred within the coordination polyhedra. Deviation of the z positional parameters from their theoretical values for the A and Ti atoms indicate that in the titanates with the larger A ²⁺ cations and Goldschmidt tolerance factors, t ≥ 0.745, the AO₆ octahedral layer is more “puckered” above and below planes parallel to (001) than that of the TiO₆ octahedra, and vice versa in the titanates with smaller R _A ²⁺ for which t≤0.745. Data are given for the volumes and distortion indices of all the coordination polyhedra. This study confirms the existence and stability of complex solid solutions between ordered rhombohedral titanates of Ni and first-row transition metals at ambient conditions over a range of t from 0.786 to 0.737. These experimental data suggest that the formation of ilmenite-type titanates enriched in Ni is possible in exotic mineral-forming systems at low pressure and/or in extraterrestrial rocks.  相似文献   

A relationship between tensile strength and loading stress governing the onset of mode I crack propagation obtained via numerical investigations using a bonded particle model          下载免费PDF全文

Zhenyu Han  Dion Weatherley  Ruslan Puscasu 《国际地质力学数值与分析法杂志》2017,41(18):1979-1991

Numerical models based on the discrete element method are used to study the fracturing process in brittle rock‐like materials under direct and indirect tension. The results demonstrate the capacity of the model to capture the essential characteristics of fracture including the onset of crack propagation, stable and unstable crack growth, arrest and reinitiation of fracturing, and crack branching. Simulations of Brazilian indirect tension tests serve to calibrate the numerical model, relating macroscopic tensile strength of specimens to their micromechanical breakage parameters. A second suite of simulations reveals a linear relationship between the tensile strength of specimens and the loading stress for which mode I tensile crack propagation ensues. Based on these results, a crack initiation criterion for brittle materials is proposed, prescribing the stressing conditions required to induce tensile failure. Such a criterion, if broadly applicable, provides a practical means to rapidly assess the failure potential of brittle materials under tensile loads.  相似文献   

Elemental and isotopic fractionation of Type B CAI-like liquids by evaporation     

Frank M. Richter  Philip E. Janney  Ruslan A. Mendybaev  Andrew M. Davis  Meenakshi Wadhwa 《Geochimica et cosmochimica acta》2007,71(22):5544-5564

Vacuum evaporation experiments with Type B CAI-like starting compositions were carried out at temperatures of 1600, 1700, 1800, and 1900 °C to determine the evaporation kinetics and evaporation coefficients of silicon and magnesium as a function of temperature as well as the kinetic isotope fractionation factor for magnesium. The vacuum evaporation kinetics of silicon and magnesium are well characterized by a relation of the form J = J_oe^−E/RT with J_o = 4.17 × 10⁷ mol cm⁻² s⁻¹, E = 576 ± 36 kJ mol⁻¹ for magnesium, J_o = 3.81 × 10⁶ mol cm⁻² s⁻¹, E = 551 ± 63 kJ mol⁻¹ for silicon. These rates only apply to evaporation into vacuum whereas the actual Type B CAIs were almost certainly surrounded by a finite pressure of a hydrogen-dominated gas. A more general formulation for the evaporation kinetics of silicon and magnesium from a Type B CAI-like liquid that applies equally to vacuum and conditions of finite hydrogen pressure involves combining our determinations of the evaporation coefficients for these elements as a function of temperature (γ = γ₀e^−E/RT with γ₀ = 25.3, E = 92 ± 37 kJ mol⁻¹ for γ_Si; γ₀ = 143, E = 121 ± 53 kJ mol⁻¹ for γ_Mg) with a thermodynamic model for the saturation vapor pressures of Mg and SiO over the condensed phase. High-precision determinations of the magnesium isotopic composition of the evaporation residues from samples of different size and different evaporation temperature were made using a multicollector inductively coupled plasma mass spectrometer. The kinetic isotopic fractionation factors derived from this data set show that there is a distinct temperature effect, such that the isotopic fractionation for a given amount of magnesium evaporated is smaller at lower temperature. We did not find any significant change in the isotope fractionation factor related to sample size, which we interpret to mean that recondensation and finite chemical diffusion in the melt did not affect the isotopic fractionations. Extrapolating the magnesium kinetic isotope fractionations factors from the temperature range of our experiments to temperatures corresponding to partially molten Type B CAI compositions (1250-1400 °C) results in a value of α_Mg ≈ 0.991, which is significantly different from the commonly used value of .  相似文献   

Nature of graphitization and noble metal mineralization in metamorphic rocks of the northern Khanka Terrane, Primorye     

A. I. Khanchuk  L. P. Plyusnina  A. V. Ruslan  G. G. Likhoidov  N. N. Barinov 《Geology of Ore Deposits》2013,55(4):225-244

Elevated contents of noble metals (NM) have been established in the Riphean-Cambrian graphite-bearing complexes of the northern Khanka Terrane, which metamorphosed under conditions of greenschist to granulite facies. At the previously known graphite deposits of the Turgenevo-Tamga group, NM comprise (ppm): Pt (0.04–62.13), Au (0.021–26), Ag (0.56–4.41), Pd (0.003–5.67), Ru (0.007–0.2), Rh (0.001–0.74), Ir (0.002–0.55), and Os (0.011–0.09). Analyses of graphitized rocks carried out with various methods (IMS, INAA, AAS, AES, fire assay) reveal a wide scatter of the results related to the specifics of sample preparation, in particular, due to a significant loss of NM by thermal oxidation decomposition. Analysis of a low-soluble graphite residue obtained by treatment of graphitized rocks allowed us to establish genetic links between NM mineralization and carbonic alteration of various igneous, granulite- and amphibolitefacies metamorphic rocks, which occur over a vast area. The nonuniform distribution of graphite and NM in rocks, their fine dispersivity, and compositional variability of NM indicate that their origin is related largely to endogenic processes with the participation of deep reduced fluids. In greenschist-facies rocks, fluorine, bromine, and iodine are associated both with ore minerals and graphite, providing evidence for transport of NM by halogene- and carbon-bearing fluids. The inhomogeneous distribution of metals in graphite, microglobular structure, and carbon isotopic composition are the guides for its gas-condensate crystallization. At the same time, thermal analysis and Raman spectroscopy show that graphite formed by metamorphism of carbonaceous matter contained in sedimentary rocks also occurs. It is concluded that the predominant mass of NM is of fluid-magmatic origin with the participation of exogenic and metamorphic sources of metals.  相似文献   

Fission–track Ages and Magnetic Susceptibility of Cretaceous to Paleogene Volcanic Rocks in Southeastern Sikhote Alin, Far East Russia     

Takaaki MaTSUDA  Tohru SAKIYAMA  Ryo ENAMI  Yo–ichiro OTOFUJI  Vladimir G. SAKHNO  Anatoly P. MATUNIN  Ruslan G. KULINICH  Petr S. ZIMIN 《Resource Geology》1998,48(4):285-290

Abstract: Seven zircon fission-track ages and 30 magnetic susceptibilities were measured on welded pyroclastic rocks from the Bogopol and Sijanov Groups of the Cretaceous to Paleogene volcanic rocks in the southeastern part of the eastern Sikhote Alin volcano-plutonic belt, Far East Russia. The fission-track ages range from 42. 7 Ma to 64. O Ma which indicate that both the groups are of Early Paleogene time. Two thirds of the samples from the Bogopol Group have high magnetic susceptibility values, more than 3 A- 10^-3 SI unit, which imply that they are of the magnetite–series, whereas the samples from the Sijanov Group show 3 A- 10^-3 to 8 A- 10^-5 SI unit which suggest this group of probably the ilmenite-series.
The Paleogene age and high magnetic susceptibility of the Bogopol Group are quite similar to the Paleogene igneous rocks of the San'in belt, Southwest Japan. This suggests, taking accounts of the opening of the Japan Sea, that the eastern Sikhote Alin volcano-plutonic belt continued to the San'in Belt, and that the Paleogene igneous rocks along the Japan Sea coast of Northeast Japan were situated along the volcanic front of the eastern Sikhote Alin volcano-plutonic belt.  相似文献