We report data on the geology, mineralogy, petrography, and chemistry of 733 Ma gabbro-peridotite sills from the Late Riphean Dovyren plutonic complex. Thick sills were differentiated into plagiolherzolite to olivine gabbronorite compositions by fractional crystallization of the K–Na series high-Mg low-alkali low-Ti picritic parental magma. The magma already contained up to 5% of intratelluric olivine crystals when entering the reservoir. The sills emplaced before the whole complex, judging by the presence of their fragments as plagiolherzolite xenoliths in the gabbro zone of the Yoko-Dovyren layered pluton. The gabbro-peridotite sills are products of high-temperature within-plate magmatism. High heat flow during the generation of the magma, evident from its high-Mg composition, was likely maintained by the activity of a mantle plume associated with the Neoproterozoic Franklin large igneous province.

New data are presented on the geologic structure, age, petrogeochemical composition, and conditions of formation of the Late Proterozoic Meteshikha ultramafic–mafic pluton of the Ikat complex. Mafic rocks are the main rocks of the massif, whereas ultramafic rocks are secondary; both of them correspond to two intrusive phases. The first phase includes a layered rock series enriched in intercumulus amphibole, which varies in composition from olivine gabbro to leucocratic gabbro-anorthosite; the second is composed of wehrlite, plagiowehrlite, and olivine clinopyroxenite. Mineralogical, petrographic, geochemical, and isotope studies show that the rocks of both phases crystallized from the same mantle melt; note that the PT-conditions of their formation were considerably different. We suppose that they were separated in the intermediate chamber during fractional crystallization and the accumulation of early minerals (olivine and, probably, clinopyroxene) in the lower part of the chamber. Using the COMAGMAT software, we have found the composition of the parental melt for the rocks of the first phase—normal tholeiitic basalt with 0.2–0.5 wt.% water, which might have crystallized at 3.0–3.5 kbar and the oxygen activity controlled by the QFM buffer. The differentiated series is characterized by gradual depletion with Cr and Ni and enrichment with Sr, Ti, Cu, and REE during the evolution of melt. The REE patterns for the massif rocks have a similar low-fractionation trend with domination of light lanthanides over heavy ones and (La/Yb)N = 1.25–2.75. Multielement spectra are characterized by negative anomalies of K, Th, Nb, and Zr and positive anomalies of Ba, U, Sm, and Sr. The geochemical characteristics of the rocks are similar to those of the tholeiitic basalts of present-day island arcs. Studies show that the Meteshikha massif formed in the subduction setting of the active margin of the Siberian continent in the Late Riphean (809 Ma). © 2015, V.S. Sobolev IGM, Siberian Branch of the RAS. Published by Elsevier B.V. All rights reserved.

Pyroxenite and nepheline-pyroxene rocks coexist with dolomite-bearing calcite marbles in Tazheran Massif in the area of Lake Baikal, Siberia, Russia. Pyroxenites occur in a continuous elongate zone between marbles and beerbachites (metamorphosed gabbro dolerites) and in 5 cm to 20 m fragments among the marbles. Pyroxene in pyroxenite is rich in calcium and alumina (5–12 wt% Al2O3) and has a fassaite composition. The Tazheran pyroxenite may originate from a mafic subvolcanic source indicated by the presence of remnant dolerite found in one pyroxenite body. This origin can be explained in terms of interaction between mafic and crust-derived carbonatitic melts, judging by the mineralogy of pyroxenite bodies and their geological relations with marbles. According to this model, the intrusion of mantle mafic melts into thick lower crust saturated with fluids caused partial melting of silicate-carbonate material and produced carbonate and carbonate-silicate melts. The fassaite-bearing pyroxenite crystallized from a silicate-carbonate melt mixture which was produced by roughly synchronous injections of mafic, pyroxenitic, and carbonate melt batches. The ascending hydrous carbonate melts entrained fragments of pyroxenite that crystallized previously at a temperature exceeding the crystallization point of carbonates. Subsequently, while the whole magmatic system was cooling down, pyroxenite became metasomatized by circulating fluids, which led to the formation of assemblages with garnet, melilite, and scapolite.