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Vol 27, No 4 (2019)

Article

Early Cambrian Syenite and Monzonite Magmatism in the Southeast of the East European Platform: Petrogenesis and Tectonic Setting

Nosova A.A., Voznyak A.A., Bogdanova S.V., Savko K.A., Lebedeva N.M., Travin A.V., Yudin D.S., Page L., Larionov A.N., Postnikov A.V.

Abstract

Abstract—The paper reports new geochronological, petrological, and isotope-geochemical data on the syenites and alkali syenites of the Artyushki massif, and the monzonites of the Gusikha massif. These massifs are located along the southwestern and northeastern margins of the Pachelma aulacogen, in the southeastern part of the East European Platform (EEP). They have Early Cambrian ages of 524 ± 3 (Artyushki) and 514 ± 2 Ma (Gusikha) obtained by the U-Pb zircon method and similar ages of amphibole and K-feldspar by the 40Ar/39Ar method. This time period has previously been regarded as amagmatic in the EEP evolution. The Artyushki massif is made up of Amp–Cpx syenite porphyries and Grt–Cpx alkali syenite porphyries and their fenitized varieties. As compared to the Amp–Cpx varieties the Grt–Cpx rocks are more peralkaline (A/NK > 0.9) and have higher LREE and HFSE, and fractionated HREE patterns. The metasomatized (fenitized) varieties are more potassic and bear geochemical evidence of fluid reworking (high Y/Ho ratios, significant Zn variations, and etc.). Bulk samples have weakly radiogenic Sr isotopic compositions: (87Sr/86Sr)520 are within 0.703066–0.703615. The values of εNd(520) vary from –0.69 to +1.64. The Grt–Cpx syenite porphyries have the positive εNd(520), while the Amp–Cpx and fenitized syenite porphyries feature negative εNd. The Gusikha massif consists of biotite–amphibole and biotite monzonites. Similar to the Artyushki syenites in SiO2 contents, the Gusikha monzonites have higher Mg# (0.22–0.54 and 0.34–0.71 for the Artyushki and Gusikha massifs, respectively). They are also characterized by a negative Nb–Ta anomaly (Nb/Nb* = 0.5), high Ва/Sr ratio, and highly radiogenic (87Sr/86Sr)520 = 0.705204 and 0.705320. Their Nd-isotopic compositions correspond to εNd(520) = –6.7 and ‒7.0. Two melts contributed to the formation of the Artyushki massif. One was a strongly contaminated melt (Amp–Cpx syenite porphyries, the other was weakly contaminated (Grt–Cpx syenite porphyries). The main contribution was phonolitic melt derived from the melting of a moderately metasomatized (carbonate- and amphibole-bearing) shallow lithospheric mantle. The earliest and deepest melt portions were carbonate–silicate in composition. The geochemical, as well as the Sr and Nd isotopic compositions of the Gusikha monzonites indicate a predominant crustal contribution and pervasive reworking of the lithospheric mantle beneath southeastern Volgo–Uralia of the EEP in the Mesoproterozoic. Both massifs feature the geochemistry of within-plate and supra-subduction derivatives, which suggests a postorogenic tectonic setting of the magmatism. The presence of the Early Cambrian postorogenic magmatism within the East European Platform/Baltica is direct evidence for the involvement of Baltica in the collisional and/or accretionary events during the terminal Neoproterozoic–the beginning of the Paleozoic. This suggests reworking of the lithospheric mantle of Baltica during its collision with Timanian and East Avalonian/Cadomian terranes, including Scythia.

Petrology. 2019;27(4):329-369
pages 329-369 views

X-Ray Computed Tomography as a Method for Reproducing 3D Characteristics of Sulfides and Spinel Disseminated in Plagiodunites from the Yoko-Dovyren Intrusion

Korost D.V., Ariskin A.A., Pshenitsyn I.V., Khomyak A.N.

Abstract

The paper describes a methodology of applying X-ray computed tomography (CT) in studying textural–morphological characteristics of sulfide-bearing ultramafic rocks from the Yoko-Dovyren layered massif in the northern Baikal area, Buryatia, Russia. The dunites are used to illustrate the applicability of a reliable technique for distinguishing between grains of sulfides and spinel. The technique enables obtaining statistical characteristics of the 3D distribution and size of the mineral phases. The method of 3D reconstructions is demonstrated to be applicable at very low concentrations of sulfides: no less than 0.1–0.2 vol %. Differences between 3D models are determined for sulfide segregations of different size, in some instances with features of their orientation suggesting the direction of percolation and accumulation of the sulfide liquids. These data are consistent with the morphology of the largest sulfide segregations, whose concave parts adjoin the surface of the cumulus olivine and simultaneously grow into grains of the poikilitic plagioclase. Detailed information of these features is useful to identify fingerprints of infiltration and concentration of protosulfide liquids in highly crystallized cumulate systems.

Petrology. 2019;27(4):370-385
pages 370-385 views

First-Principles Determination of Oxygen and Silicon β-Factors for Zircon

Krylov D.P.

Abstract

The temperature dependence of the β-factors of zircon was determined for 18O/16O and 30Si/28Si isotopic substitutions. Calculations were performed on the basis of the density functional theory (DFT) using the frozen phonon approach. The obtained geometric parameters of the zircon crystal lattice and vibrational frequencies are in good agreement with experimental data. The results were approximated by the following cubic polynomials in x = 106/T(K)2: 1000 ln βzrn(18O/16O) = 9.83055x – 0.19499x2 + 0.00388x3 and 1000 ln βzrn(30Si/28Si) = 7.89907x – 0.17978x2 + 0.00377x3. The obtained relations can be used in combination with the β-factors of other phases for the construction of geothermometers. New calibrations of the quartz–zircon isotope geothermometer were proposed. The obtained 1000 ln βzrn values and isotope fractionation factors between quartz and zircon (1000 ln βqtz – 1000 ln βzrn) are significantly different from those obtained by previous experimental, empirical, and semiempirical calibrations of isotope equilibria.

Petrology. 2019;27(4):386-394
pages 386-394 views

Equation of State of the H2O–CO2–CaCl2 Fluid System and Properties of Fluid Phases at Р-Т Parameters of the Middle and Lower Crust

Ivanov M.V., Bushmin S.A.

Abstract

A numerical thermodynamic model is proposed for one of the most important geological fluid system, ternary H2O–CO2–CaCl2 system, at P-T conditions of the middle and lower crust and crust–mantle boundary. The model is based on the previously proposed equation for concentration dependence of the excess Gibbs free energy and on the first obtained P-T dependencies of the coefficients of the equation of state (EOS) expressed via molar volumes of the components. The EOS allows to predict the properties of the fluid participating in the majority of deep petrogenetic processes: its phase state (homogeneous or multi-phase), densities of fluid phases, concentrations of components in the co-existing phases, and the chemical activities of the components. The model precisely reproduces all available experimental data on the phase state of the ternary H2O–CO2–CaCl2 fluid system in the ranges of temperatures 773.15–1073.15 K and pressures 0.1–0.9 GPa and also allows the correct application of the EOS beyond the experimentally studied range of temperatures and pressures up to P = 2 GPa and T = 1673.15 K. The possibility of the correct extrapolation of our EOS is ensured by using the parametrization of P-T dependencies via the molar volume of water. The latter remains in the experimental domain of values or falls slightly beyond its boundaries, when increasing temperatures and pressures.

Petrology. 2019;27(4):395-406
pages 395-406 views

Behavior of the 238U, 235U, and 234U Isotopes at Weathering of Volcanic Rocks with U Mineralization: A Case Study at the Tulukuevskoe Deposit, Eastern Transbaikalia

Chernyshev I.V., Golubev V.N., Chugaev A.V., Mandzhieva G.V., Gareev B.I.

Abstract

The trend fractionation of the 238U and 235U isotopes and the extent of this process at the oxidative weathering of uranium minerals were evaluated by studying the variations in the U isotope composition of rocks, minerals, and fracture waters sampled in the quarry of the broadly known Tulukuevskoe uranium deposit in the Streltsovskoe ore field, eastern Transbaikalia. In the rock block in question, fine uranium minerals disseminated in the rocks were weathered under the effect of oxidizing fracture waters. Uranium isotope composition was measured in 22 water samples, eleven samples of the mineralized rocks, and eight uranium minerals. High-precision (±0.07‰, 2SD) measurements of the 238U/235U were carried out by MC-ICP-MS, using a 233U–236U double spike. The results involve the 238U/235U and 234U/238U ratios and the overall range of the δ238U variations determined in the rocks and waters (from –0.13 to –1.0‰ and from –0.22 to –0.59‰, respectively). Interaction between the waters and rocks induces U(IV) → U(VI) oxidation, U(VI) transfer into the aqueous phase, and 0.15–0.28‰ enrichment of U dissolved in the water in the 235U isotope. When the pitchblende is replaced by U(VI) minerals, the 238U and 235U isotopes also fractionate with ~0.3‰ enrichment of the younger U(VI) mineral phases in the light 235U isotope. The 238U/235U and 234U/238U ratios are proved to correlate, and hence, the fractionation of the 238U and 235U isotopes and the enrichment of the aqueous phase in the light 235U isotope proceed simultaneously with the well known shift in equilibrium the 238U–234U system with the accumulation of excess amounts of the 234U in the aqueous phase. Uranium leaching from uranium minerals, which is associated with the enrichment of the aqueous phase in excess amounts of the 234U isotope, can be viewed as a process that controls isotope fractionation in the 238U–235U system. This should be taken into account in describing the fractionation mechanism of the 238U and 235U isotopes at U(IV) → U(VI) oxidation. The fractionation of the 238U and 235U isotopes, which results in the isotopic “lightening” of U in the aqueous phase, largely controlled the complicated distribution pattern of the 238U/235U ratio in the quarry. In addition to isotope fractionation, this distribution was likely also affected by isotope exchange between uranium dissolved in the water and uranium in the finely dispersed minerals. The isotopically light uranium of the water could participate in forming U(VI) minerals at lower levels of the quarry.

Petrology. 2019;27(4):407-424
pages 407-424 views

The Timing of the Paleo-Asian Oceanic Closure: Geochemical Constraints from the Jigede Gabbro in the Alxa Block

Zheng Liu ., Zhang X., Tan S., Sha X., He X., Zhou Q.

Abstract

This paper investigates the Jigede gabbros from the Shalazhashan tectonic belt, Alxa Block. Laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) zircon U-Pb dating reveals that they were emplaced in the Middle Permian (ca. 262 Ma). All the gabbro samples collected from the intrusion exhibit low contents of TiO2 (0.24–0.37 wt %) and \({\text{F}}{{{\text{e}}}_{{\text{2}}}}{\text{O}}_{{\text{3}}}^{{\text{T}}}\) (4.87–5.41 wt %), but high levels of MgO (11.15–12.15 wt %), CaO (11.45–12.75 wt %), Al2O3 (14.18–17.08 wt %) and high Mg# (0.81–0.83). Relative to HREEs and LILEs, the gabbros are enriched in LREEs and depleted in Th, Nb, Ce, Zr, Hf, and Ti, with positive Eu, Sr and U anomalies. In contrast to MORB, the Jigede intrusion has higher initial 87Sr/86Sr values of 0.7046 to 0.7054 and lower εNd(T) of + 1.8 to + 4.8. Elemental and isotopic data suggest that the intrusion was likely to have been produced by partial melting of a shallow lithospheric mantle source modified by slab-derived fluids, with subsequent cumulation of plagioclase. Thus, the Jigede intrusion was emplaced in a back-arc setting, in response to the Paleo-Asian oceanic subduction. In addition, the final closure of the Paleo-Asian Ocean did not occur prior to the Middle Permian.

Petrology. 2019;27(4):425-437
pages 425-437 views