Том 56, № 6 (2018)

This paper reports Rb–Sr and Sm–Nd isotope data on the gabbro–diorite–tonalite rock association of the Reft massif (eastern margin of the Middle Urals) and Lu–Hf isotope data on zircon populations from these rocks. In terms of Nd and Hf isotope composition, the rocks of the studied association are subdivided into two distinctly different groups. The first group consists of gabbros and diorites, as well as plagioclase granites from thin dikes and veins cutting across the gabbros. In terms of ⁴³Nd/¹⁴⁴Nd_i = 0.512518–0.512573 (ε_Nd(T) = +8.6...+9.7) and ¹⁷⁶Hf/¹⁷⁷Hf_i = 0.282961–0.283019 (ε_Hf(T) = +15.9...+17.9), these rocks are practically identical to depleted mantle. Their Nd and Hf model ages show wide variations, but in general are close to their crystallization time. The second group is represented by tonalites and quartz diorites, which compose a large body occupying over half of the massif area. These rocks are characterized by the lower values of ¹⁴³Nd/¹⁴⁴Nd_i = 0.512265–0.512388 (ε_Nd(T) = +3.7...+6.0) and ¹⁷⁶Hf/¹⁷⁷Hf_i = 0.282826–0.282870 (ε_Hf(T) = +11.1...+12.7). The T_DM values of the second group are much (two–three times) higher than their geological age (crystallization time), which indicates sufficiently long crustal residence time of their source. The initial ⁸⁷Sr/⁸⁶Sr in the rocks of both the groups varies from 0.70348 to 0.70495. This is likely explained by the different saturation of melts with fluid enriched in radiogenic Sr. The source of this fluid could be seawater that was buried in a subduction zone with oceanic sediments and released during slab dehydration. Obtained data make it possible to conclude that the formation of the studied gabbro–diorite–tonalite association is a result of spatially and temporally close magma formation processes in the crust and mantle, with insignificant contribution of differentiation of mantle basite magma.

Fluoro-sodalite was synthesized for the first time at temperatures of 400–800°C and H₂O pressures of 1–2 kbar in the Si–Al–Na–H–O–F system. X-ray diffraction and infrared spectroscopic investigations showed that fluorine is incorporated in the sodalite structure as anionic octahedral groups, [AlF₆]^3–, the number of which can vary from 0 to 1. Correspondingly, the end-members of the F-sodalite series are Na₇(H₂O)₈[Si₅Al₇O₂₄] and Na₈(AlF₆)(H₂O)₄[Si₇Al₅O₂₄]. Depending on the composition of the system, F-sodalite associates at 500–650°C with nepheline, albite, cryolite, and villiaumite, which are joined by analcime below 500°C and aluminosilicate melt above 650°C. Fluorine-bearing sulfate–chlorine-sodalite was found for the first time in a pegmatite sample from the Lovozero massif. The highest fraction of the fluorine end-member in natural sodalite is 0.2. The incorporation of F into the sodalite structure requires much more energy compared with Cl^– and SO₄^2-, because it is accompanied by a structural rearrangement and a transition from tetrahedral Al to octahedral Al.

This paper analyzes differences in the history of hydrocarbon (HC) generation by the rocks of the Bremer 1–6 formations in adjacent areas of the nonvolcanic passive continental margins of Australia and Antarctica. The problem is examined by the example of the numerical reconstruction of the burial and thermal history of two sedimentary sequences of approximately equal thicknesses: the section of well 19–2012 in the Bremer sub-basin of the southwestern margin of Australia and the section of pseudowell 2 in the adjacent area of the passive margin of Antarctica on seismic profile 5909 across the Mawson Sea. The asymmetry of Gondwana rifting in the region of interest resulted in asymmetry in the tectonic structure and development of adjacent areas of passive margins and, as a consequence, significantly different histories of HC generation by the rocks of the Bremer 1–6 formations in these areas. Modeling indicates that the rocks of the Bremer 1 and 2 formations are mainly gas-prone in the Bremer basin and can become oil-prone in the Mawson Sea region of the Antarctic margin. In contrast, according to modeling, the rocks of the Bremer 4 and 5 formations generate a minor amount of HC in the well 19–2012 area of the Bremer sub-basin and considerable amounts of heavy and light oil in the adjacent Antarctic margin area at pseudowell 2 in the Mawson Sea.

This study defines the source area, sub-aerial weathering, and sedimentary cycle level, as well as heavy metal content and origin, of the Çoruh River bed sediments. The studied sediments are geochemically classified as litharenite based on the ratio of the major element contents. Relative to the Upper Continental Crust (UCC), trace elements Rb, Sr, Ba, Th, U, Zr, Hf, Y, Nb, and Pb are generally depleted; Co, Ni, Cu, Sc, and V are generally enriched; and Au is depleted in some places and enriched in other places. The rare earth element (REE) distributions of the samples exhibit a trend similar to that of the upper continental crust (UCC); however, low to moderate depletion occurs in the bed sediments in UCC. The analyzed samples exhibit low Chemical Index of Alteration (CIA) values, Plagioclase Index of Alteration (PIA) values (<50), CIA/WIP (Weathering Index ratios <1), and substantially high Index of Compositional Variability values (ICV) (>1). Thus, the samples are not chemically mature and are mainly derived from non-altered sources and were exposed the simple cycling history. REEs are depleted in the river bed sediments, unlike the world river average silt, world river average clay, and suspended sediment in world rivers. Minor enrichment of Zn, Sn, and Sc contents, low-to-moderate enrichment of Cu content, very severe enrichment of as content, and extremely severe enrichment of Ni content of the analyzed samples are observed. Consequently, stream bed sediments are derived from intermediate sources close to mid-continental crust rather than felsic sources Low-to-moderate degrees of chemical weathering of these sediments indicate increased tectonic activity, increased erosion, and rapid sedimentation in semiarid to arid conditions in the source regions over time. Thus, the sediments are chemically immature. These sediments are exposed to lithogenic and anthropogenic contamination.

The distribution of ions of organic carboxylic acids (formic, acetic, and oxalic) was investigated in the snowpack of permafrost landscapes of the boreal zone of Eastern Siberia. The contents of formate-, acetate-, and oxalate-ions were determined in permafrost landscapes of different zones of latitudinal and mountain- belt types. The maximum contents of organic carboxylic acid ions were observed in the snow cover of middle-taiga landscapes. The input rate of the ions into the snow cover of middle-taiga and mountain landscapes is controlled by altitudinal zonation and correlates with the total mass of plant organisms, which are the main source of organic carboxylic acids in the atmosphere. The obtained data suggest that organic carboxyl acid ions were supplied mainly by the atmosphere (74–90%), whereas the contribution of soil respiration was minor. The upward migration of organic carboxylic acid ions from the substrate to the snow cover depends on soil and snow temperature. Cooling of the soil surface below–5°C results in a considerable decrease in the migration of organic carboxylic acid ions from soil to snow.