Radiocarbon dating of small landslides on the slopes of the Mzymta River valley

This paper reports the results of the first study aimed at determination of the age of landslides on the southern slope of the Psekhako Ridge and northern slope of the Aibga Ridge (Western Caucasus) using radiocarbon dating of organic material incorporated into the landslide body.     

Application of thermodesorption mass spectrometry for studying proton water formation in the lunar regolith

In this paper, we report experimental data on the implantation of hydrogen ions of different energies into crystalline quartz samples. It was shown that irradiation with protons with an energy of 20 keV produces an amorphous film on the surface of a quartz sample, and irradiation with 90-keV protons results in the formation of a layer with interstitial defects and an increase in the unit-cell parameter of quartz with preservation of the crystal structure of the disturbed layer. The examination of the samples by thermodesorption mass spectrometry showed that high-energy irradiation resulted also in loosening of the surface layer and considerable expansion of high-potential adsorption sites, which was the reason for the observed peak desorption of gases. The existence of desorption peaks allowed us to calculate the activation energy of surface desorption of gas components. It was also found that an increase in irradiation energy tends to enhance the total degassing of samples.     

CrystalMom: a new model for the evolution of crystal size distributions in magmas with the quadrature-based method of moments

Nucleation and growth of crystals, and the resulting crystal size distribution, play a fundamental role in controlling the physical properties of magmas and consequently the dynamics of the eruptions. In the past decades, laboratory experiments demonstrated that size and shape of crystals strongly control the physical properties of magma and lava. Additionally, natural and experimental samples are usually characterized in terms of their crystal size distribution to link it with physical processes that are not directly observable, such as cooling or decompression mechanisms. In this paper, we present CrystalMoM, a new predictive model, based on the quadrature-based method of moments, developed for studying the kinetic of crystallization in volcanic systems. The quadrature-based method of moments, well established in the field of chemical engineering, represents a mesoscale modelling approach that rigorously simulates the space–time evolution of a distribution of particles, by considering its moments. The method is applied here, for the first time, for studying the equilibrium/disequilibrium crystallization in magma, modelling the temporal evolution of the moments of a crystal size distribution. The model, verified against numerical and experimental data, represents a valuable tool to infer the cooling and decompression rates from the crystal size distribution observed in natural samples.     

Thermodynamic controls on element partitioning between titanomagnetite and andesitic–dacitic silicate melts

Titanomagnetite–melt partitioning of Mg, Mn, Al, Ti, Sc, V, Co, Ni, Cu, Zn, Ga, Zr, Nb, Mo, Hf and Ta was investigated experimentally as a function of oxygen fugacity (fO₂) and temperature (T) in an andesitic–dacitic bulk-chemical compositional range. In these bulk systems, at constant T, there are strong increases in the titanomagnetite–melt partitioning of the divalent cations (Mg²⁺, Mn²⁺, Co²⁺, Ni²⁺, Zn²⁺) and Cu²⁺/Cu⁺ with increasing fO₂ between 0.2 and 3.7 log units above the fayalite–magnetite–quartz buffer. This is attributed to a coupling between magnetite crystallisation and melt composition. Although melt structure has been invoked to explain the patterns of mineral–melt partitioning of divalent cations, a more rigorous justification of magnetite–melt partitioning can be derived from thermodynamic principles, which accounts for much of the supposed influence ascribed to melt structure. The presence of magnetite-rich spinel in equilibrium with melt over a range of fO₂ implies a reciprocal relationship between a(Fe²⁺O) and a(Fe³⁺O_1.5) in the melt. We show that this relationship accounts for the observed dependence of titanomagnetite–melt partitioning of divalent cations with fO₂ in magnetite-rich spinel. As a result of this, titanomagnetite–melt partitioning of divalent cations is indirectly sensitive to changes in fO₂ in silicic, but less so in mafic bulk systems.     

Formation of N–С–О–Н molecules and complexes in the basalt–basaltic andesite melts at 1.5 Gpa and 1400°C in the presence of liquid iron alloys

The contents and speciation of nitrogen, carbon, and hydrogen were determined in basalt–basaltic andesite melts in equilibrium with liquid Fe alloys at 1.5 Gpa, 1400°C, and oxygen fugacity (fO₂) 1.4–1.9 log units below that of the Fe–FeO buffer (ΔlogfO₂(IW) =–1.4 …–1.9). Experiments were carried out on a piston- cylinder type apparatus using welded Pt capsules in the presence of excess С (graphite). Starting mixture consisted of natural ferrobasaltic glass and silicon nitride (Si₃N₄) as nitrogen source in the system. Experimental quench products representing glasses with spherical inclusions of iron alloy were analyzed using electron microprobe, Raman, and IR spectroscopy. With increase of Si₃N₄ in the starting mixture and, respectively, decrease of fO₂, silicate melt forming during experiments became depleted in FeO and enriched in SiO₂. It was established that the nitrogen content in the glasses increases from 0.13 to 0.44 wt % with decrease of ΔlogfO₂(IW) from–1.4 to–1.9, whereas C content in the first approximation remains constant within 1.18–1.13 wt %, while the total water content (ОН^– + Н₂О) determined by IR spectroscopy decreases from 4.91 to 1.20 wt %. The N (0.13–0.48 wt %) and C (0.75–2.26 wt %) contents determined in the Fe alloy show no clear correlation with fO₂. The IR and Raman spectroscopic study of the glasses indicates the formation of molecules and complexes with bonds N–H (NH₃, NH₂ ^?, NH₂ ⁺, NH₄ ⁺), Н–О (Н₂О, OH^–), С–Н (СН₄) as well as N₂ and Н₂ molecules in silicate melts. IR spectra also reveal the presence of complexes with С=О, С–N bonds and СО₂ molecules. Obtained data are compared with results of previous studies on the solubility and speciation of N, С, and Н in the model FeO–Na₂O–SiO₂–Al₂O₃ melts in equilibrium with liquid iron alloys at 1.5 GPa (1400°C) and 4 GPa (1550°C) (Kadik et al., 2011, 2015).     

Sedimentary infill in the equatorial Mid-Oceanic Canyon,Atlantic Ocean

Facts confirming the hypothesis of contourite sediment infill of the Equatorial Mid-Ocean Canyon (EMOC) are presented. We examined two cores recovered in Cruises 37 and 43 of the R/V Akademik Ioffe (2012, 2013). The cores recovered upper Quaternary miopelagic clays on the EMOC floor (AI-3149) and the adjacent abyssal plain (AI-2620). The study of these cores unraveled significant differences in their composition. In contrast to the lithologically homogeneous Core AI-2620, Core AI-3149 includes interlayers enriched in the biogenic CaCO₃, terrigenous silt, and authigenic ferromanganese micronodules. These peculiarities are attributed to activity of the Antarctic Bottom Water (AABW) contour currents along the EMOC.     

The Varre-Sai chondrite,a Brazilian fall: petrology and geochemistry

The Varre-Sai meteorite fell along the border of the states of Espirito Santo and Rio de Janeiro, Brazil; on 19 June 2010 at 5:40 pm. Petrography and X-ray powder diffraction (XRD) indicate that the rock is an L5 S4 chondrite, with blastoporphyritic texture that has not been previously described. Geochemical data based on major and rare-earth elements (REEs) show that Varre-Sai is highly similar to the other L chondrites. In Harker diagrams, Varre-Sai, L, and LL chondrites form a single group, suggesting no significant chemical differences between them and contributing to the long-standing debate of whether LL chondrites form a distinct group or whether they are a subset of the L group. Harker diagrams also define a trend from E to H and L/LL chondrites, similar to the cosmochemical trends suggested by other authors. The behaviour of Fe₂O_3t and NiO indicates a relationship with Fe-Ni alloys, and their trend in the diagram suggests some chemical differentiation in the ordinary chondrite parental bodies. The REE content in Varre-Sai, normalized to C chondrites, falls in the field of L chondrites and others, but with slight REE enrichment. The chemical differences in chondrites, mainly in REEs, Fe₂O_3t and NiO could be alternatively interpreted as variations in the inherited agglutinated materials as chondrules, Ca–Al-rich inclusions and Fe–Ni nodules.     

The upper Devonian Sargaevo regional stage in the Tsil’ma River basin,Middle Timan

The results of bio- and lithostratigraphic study of Sargaevo deposits in the Tsil’ma River basin are discussed. The palynological data used for biostratigraphic subdivision of the section provide grounds for defining the miospore assemblage corresponding to the regional miospore Cristatisporites pseudodeliquescens Zone. It is established that deposits of the Sargaevo regional stage are distributed almost through the entire Tsil’ma River basin. They are characterized by distinct lithological features and may serve as a stratigraphic reference unit in field investigations.     

Taxonomic composition and biostratigraphic value of the Early Riphean organic-walled microfossil association from the Ust’-Il’ya Formation of the Anabar Uplift,Northern Siberia

It is demonstrated on the basis of the first monographic study of multiple and taxonomically variable organic-walled microfossils from the Ust’-Il’ya Formation of the Anabar Uplift that both prokaryotic and eukaryotic forms are present in the composition of this microbiota. They are divided into four formal groups on the basis of the specifics of the morphological indicators of the identified taxa. The review of the data on the isotopic age of hosting deposits showed that the Ust’-Il’ya Formation is of the Early Riphean in age which are currently evaluated as 1750 ± 10–1400 Ma. Relatively large and morphologically complex eukaryotic forms present in the Ust’-Il’ya Formation served in due time as the basis for an erroneous conclusion on the Late Riphean age of the specified formation and the overlying Lower Kotuikan Subformation of the Anabar Uplift. The paper provides a global comparative analysis of the Early Riphean microbiotas, demonstrates the position of the Ust’-Il’ya and Kotuikan microbiotas amidst the microbiotas of the same age, and shows that the relatively large acanthomorphic acritarchs Tappania, Valeria, Dictiosphaera, Satka, and Shuiyousphaeridium appeared in the geological history already during the Early Riphean Erathem. Moreover, the paper discusses the recently published data on the distribution of aerobic and anaerobic conditions in the Early Riphean paleobasins and provides the conclusion on the impact of the lateral change of these conditions on the taxonomic composition of the microbiota.