Description: Cretaceous to Eocene plutonic and volcanic rocks of the Sabzevar zone have an adakite characteristic with high Sr/Y ratio, depleted HFSE and enriched LILE features. Most of the Sabzevar adakites are high silica adakites with low Ni, Cr and Co contents. LREE/HREE ratio is high, while K 2 O content is low to intermediate. Adakites in the Sabzevar zone are exposed in two areas, which are named southern and northern adakites here. The combination of Sr, Nd and Pb isotopic data with major and trace elements indicates that the adakitic rocks are formed by partial melting of the Sabzevar oceanic slab. Nb/Ta content of the samples indicates that the adakitic magmas were generated at different depth in the subduction system. Dy/Yb ratios of adakitic samples indicate positive, negative and roughly flat patterns for different samples, suggesting garnet and amphibole as residual phases during slab-derived adakitic magma formation. Sabzevar adakites emplaced during late to post-kinematic events. Sabzevar oceanic basin demised during a northward subduction by central Iranian micro-continents (CIM) and Eurasia plate convergence.

Description: The paper presents detailed isotope-geochronological, geological, and petrologic–mineralogical data on lavas of one of the greatest Quaternary magmatic area in the Greater Caucasus, the Kazbek neovolcanic center, including polygenetic Kazbek stratovolcano and a number of subordinate volcanic cones in its vicinities. The research was conducted based on a representative collection of more than 150 geological samples that characterize most of the volcanic cones and lava flows of different age, some of which were known previously, and other were discovered by the authors. The high-precision K–Ar data obtained on these materials make it possible to reproduce the evolutionary history of youngest magmatism at the Kazbek center and evaluate the total duration of this evolution at ~450 ka. The magmatic activity was subdivided into four phases (at 460–380, 310–200, 130–90, and 〈50 ka) with long-lasting interludes in between. Because the latest eruptions occurred in the Kazbek vicinity in the Holocene, this volcano is regarded as potentially active. The volcanic rocks of the Kazbek center make up a continuous compositional succession of basaltic (trachy)andesite–(trachy)andesite–dacite and mostly belong to the calc–alkaline series. The principal petrographic characteristics of the rocks and the composition of their phenocryst minerals are determined, mineral assemblages of these minerals are distinguished in the lavas of different type, and the temperature of the magmatic melts is evaluated. A principally important role in the petrogenesis of the Kazbek youngest magmas is proved to have been played by fractional crystallization and replenishment of mafic melts in the magmatic chambers beneath the volcano, which resulted in their mixing and mingling with the residual dacite melt and the origin of high-temperature hybrid andesite lavas. The comprehensive geological studies, involving interpretation of high-resolution satellite images, allowed the authors to compile the first detailed (1: 25 000) volcanologic map of the Kazbek center and a geochronologic chart supplemented with a stratigraphic column, which illustrate the origin sequence of the volcanic vents and their lava flows, geological relations between them, as seen in reference geological sections, and variations in the composition of the magmatic products with time.

Description: Experimental investigations in the system rare-metal granite–Na 2 O–SiO 2 –H 2 O with the addition of aqueous solutions containing Rb, Cs, Sn, W, Mo, and Zn at 600°C and 1.5 kbar showed that the typical elements of rare-metal granites (Li, Rb, Cs, Be, Nb, and Ta) are preferentially concentrated in hydrosilicate liquids coexisting with aqueous fluid. The same behavior is characteristic of Zn and Sn, the minerals of which are usually formed under hydrothermal conditions. In contrast, Mo and W are weakly extracted by hydrosilicate liquids and almost equally distributed between them and aqueous fluids. Liquids similar to those described in this paper are formed during the final stages of magmatic crystallization in granite and granitepegmatite systems. The formation of hydrosilicate liquids in late magmatic and postmagmatic processes will be an important factor controlling the redistribution of metal components between residual magmatic melts, minerals, and aqueous fluids and, consequently, the mobility of these components in fluid-saturated magmatic systems enriched in rare metals.

Description: The paper presents newly obtained original data on the morphology, internal structure (as seen in cathodoluminescence images, CL), and composition of more than 400 zircon grains separated from gabbroids and plagiogranites (OPG) sampled at the axial zone of the Mid-Atlantic Ridge (MAR). The zircons were analyzed for REE by LA-ICP-MS and for Hf, U, Th, Y, and P by EPMA. Magmatic zircon in the gabbroids crystallized from differentiating magmatic melt in a number of episodes, as follows from systematic rimward increase in the Hf concentration, and also often from the simultaneous increase in the (U + Th) and (Y + P) concentrations. These tendencies are also discernible (although much less clearly) in zircons from the OPG. Zircon in the OPG is depleted in REE compared to the least modified zircons in the gabbro, which suggests that the OPG were derived via partial melting of gabbro in the presence of seawater-derived concentrated aqueous salt fluid. Another reason for the REE depletion might be simultaneous crystallization of zircon and apatite. The CL-dark sectors, which are found in practically all of the magmatic zircon grains, have Y/P (a.p.f.u.) ≫ 1 which most likely resulted from OH accommodation in the zircon structure, a fact suggesting that the OPG parental melt contained water. High-temperature hydrothermal processes induced partial to complete recrystallization of zircon (via dissolution-reprecepitation), a process that was associated with ductile and brittle deformations of the zircon-hosting rocks. The morphology of the hydrothermal zircons varies depending on pH and silica activity in the fluid from weakly corroded subhedral crystals with typical vermicular microtopography of the crystal faces to completely modified grains of colloform structure. Geochemically, the earlier hydrothermal transformations of the zircons resulted in their enrichment in La and other LREE, except only Ce, whose concentration, conversely, decreases compared to that of the unmodified magmatic zircons. The hydrothermal zircon displays a reduced Ce anomaly and its most altered domains typically host minute inclusions of xenotime, U and Th oxides and silicates, and occasionally also baddeleyite, which suggests that the hydrothermal fluid was reduced and highly alkaline. These features were acquired by the seawater-derived fluid when it circulated within the axial MAR zone area due to phase separation in the H 2 O–NaCl system and particularly as a result of fluid interaction with the abyssal peridotites of oceanic core complexes. Our data demonstrate that zircon is a sensitive indicator of tectonic and physicochemical processes in the oceanic crust.

Description: New isotopic-geochemical data are reported on the Late Cretaceous–Paleocene ultrapotassic volcanic rocks of the alkaline–ultrabasic complex of the Valagin Ridge, Eastern Kamchatka. The high Mg, low Ca and Al contents at high K/Na ratios in these rocks make them similar to the Mediterranean-type lamproites and ultrapotassic rocks. The low contents of high-field strength (HFSE) and heavy rare-earth (HREE) elements relative to the MORB composition, and the low Sr and high Nd isotopic ratios indicate the formation of their primary melts from a depleted mantle source. The enrichment of the ultrapotassic rocks in the large-ion lithophile elements (LILE) can be explained by the fluid influx in melts during melting of subsided oceanic crust.

Description: Fragments of heterogeneous cosmonegic substance (nickelphosphide Ni 3 P and ZnAl 2 ) were found using high resolution analytical electron microscopic techniques, for the first time in samples from a large meteorite crater: the Zhamanshin astrobleme in Kazakstan. Inasmuch as such fragments cannot simultaneously occur in meteorite of any one type, we suggest that the impactor of the Zhamanshin crater was of comet nature.

Description: The Tuva–Mongolian terrane of the Central Asian Orogenic Belt is a composite structure with a Vendian–Cambrian terrigenous–carbonate cover. The Sangilen block in the southern part of the belt is a smaller composite structure, in which tectono–stratigraphic complexes of different age that were produced under various conditions were amalgamated in the course of Early Paleozoic tectonic cycle. The P–T parameters of the Early Paleozoic metamorphism in the western part of the Sangilen block corresponded to the amphibolite facies. The gneisses of the Erzin Complex contain relict granulite-facies mineral assemblages. The granulites are dominated by metasediments typical of deep-water basins on passive continental margins. The only exception is granulites of the Lower Erzin tectonic nappe of the Chinchlig thrust system: these rocks are metatholeiites, tonalites, and trondhjemites, whose REE patterns are similar to those of MORB. The composition of these granulites and their high Sm/Nd ratios indicate that the rocks were derived from juvenile crust that had been formed in an environment of a mature island arc or backarc basin. It is reasonable to believe that these rocks are fragments of the Late Riphean basement of the Sangilen block. The average 206 Pb/ 238 U zircon age of the garnet–hypersthene granulites is 494 ± 11 Ma. With regard for the zircon age of the postmetamorphic granitoids, the granulite-facies metamorphism occurred within the age range of 505–495 Ma. The peak metamorphic temperature reached 910–950°C, and the pressure was 3–4 kbar, which corresponds to ultrahigh-temperature/low-pressure (UHT–LP) metamorphism. The garnet–hypersthene orthogranulites were formed at a temperature that decreased to ~850°C and pressure that increased to ~5.5‒7 kbar. It can be hypothesized that the earlier UHT–LP granulites were produced at an elevated heat flux and were later (in the course of continuing collision) overlain by a relatively cold tectonic slab, and this leads to a certain temperature decrease and pressure increase. This relatively cold slab could consist of fragments of the Vendian elevated-pressure metamorphic belt whose development terminated at the Vendian–Cambrian boundary before the onset of the Early Paleozoic regional metamorphism.

Description: Titanium contents of quartz have been analyzed in samples of granulites from various metamorphic complexes of eastern Siberia (Sutam, Chogar, and Sharyzhalgai) that contain mineral assemblages conventionally regarded as indicative of “ultrahigh-temperature” metamorphism. The related TitaniQ temperature estimates (Wark and Watson, 2006) are consistent with those of other mineralogical geothermometers and are commonly much lower than “ultrahigh-temperature”.

Description: Reactions and partial melting of peraluminous rocks in the presence of H 2 O-CO 2 –salt fluids under parameters of granulite-facies metamorphism were modeled in experiments on interaction between orthopyroxene–cordierite–biotite–plagioclase–quartz metapelite with H 2 O, H 2 O-CO 2 , H 2 O-CO 2 -NaCl, and H 2 O-CO 2 -KCl fluids at 600 MPa and 850°C. Rock melting in the presence of H 2 O and equimolar H 2 O-CO 2 fluids generates peraluminous (A/CNK 1 〉 1.1) melts whose composition corresponds to magnesian calcic or calc–alkaline S-type granitoids. The melts are associated with peritectic phases: magnesian spinel and orthopyroxene containing up to 9 wt % Al 2 O 3 . In the presence of H 2 O-CO 2 -NaCl fluid, cordierite and orthopyroxene are replaced by the association of K-Na biotite, Na-bearing gedrite, spinel, and albite. The Na 2 O concentrations in the biotite and gedrite are functions of the NaCl concentrations in the starting fluid. Fluids of the composition H 2 O-CO 2 -KCl induce cordierite replacement by biotite with corundum and spinel and by these phases in association with potassium feldspar at X KCl = 0.02 in the fluid. When replaced by these phases, cordierite is excluded from the melting reactions, and the overall melting of the metapelite is controlled by peritectic reactions of biotite and orthopyroxene with plagioclase and quartz. These reactions produce such minerals atypical of metapelites as Ca-Na amphibole and clinopyroxene. The compositions of melts derived in the presence of salt-bearing fluids are shifted toward the region with A/CNK 〈 1.1, as is typical of so-called peraluminous granites of type I. An increase in the concentrations of salts in the fluids leads to depletion of the melts in Al 2 O 3 and CaO and enrichment in alkalis. These relations suggest that the protoliths of I-type peraluminous granites might have been metapelites that were melted when interacting with H 2 O-CO 2 -salt fluids. The compositions of the melts can evolve from those with A/CNK 〉 1.1 (typical of S-type granites) toward those with A/CNK = 1.0–1.1 in response to an increase in the concentrations of alkali salts in the fluids within a few mole percent. Our experiments demonstrate that the origin of new mineral assemblages in metapelite in equilibrium with H 2 O-CO 2 -salt fluids is controlled by the activities of alkaline components, while the H 2 O and CO 2 activities play subordinate roles. This conclusion is consistent with the results obtained by simulating metapelite mineral assemblages by Gibbs free energy minimization (using the PERPE_X software), as shown in log( \({a_{{H_2}O}}\) )–log( \({a_{N{a_2}O}}\) ) and log( \({a_{{H_2}O}}\) )–log( \({a_{{K_2}O}}\) ) diagrams.

Description: The paper discusses petrological effects related to interaction between rocks and concentrated aqueous salt fluids (brines) at lower crustal metamorphism. These effects arise mainly from the low H 2 O activity typical of brines, while preserving and even increasing transport properties relative to pure H 2 O or H 2 O–nonpolar gas fluids. The paper presents thermodynamic properties of the halogen-bearing end members of the biotite solid solution based on experimental data, and examples illustrating how they can be employed to calculate the activities (concentrations) of alkali halides in the fluid. Action of brines significantly changes conventional views on the solubility of several minerals and on the distribution of elements (including trace elements) between minerals, melts, and fluids. The specific role of brines is also in bringing to interaction zones not only water but also alkali metals and Ca, which results in numerous metasomatic net-transfer reactions involving mafic minerals and/or exchange reactions with feldspars that produce new mineral assemblages with lower melting temperature, i.e., cause granitization of rocks as defined by D.S. Korzhinskii. Brines also exert fine “tuning” of metasomatic and melting processes: even at equal pressure, temperature, and water activity values metasomatism may or may not trigger melting depending on the Na/K/Ca ratio in the fluid phase.