Chemical composition,isotopic U–Pb age,and source of zircon from polymineralic ichet’yu occurrence,Mobile Timan

This study focuses on the morphological features, color cathodoluminescence, chemical composition, age, and source of zircons from the Ichet’yu occurrence. The isotopic U–Pb age of Paleo–Mezoproterozoic zircon grains varies within an interval of ~700 Ma from 2247 to 1478 Ma. The average roundness and well-preserved integrity of zircon grains allow us to suggest their proximal source. The available data show that the basement of the Middle Timan, composed of continental Paleo–Mezoproterozoic igneous rocks, is the most probable source of zircon in the Ichet’yu occurrence. These rocks are apparently a continuation of the Archean–Proterozoic Arkhangel’sk Mobile Belt.     

Abnormal composition of carbon isotopes in underground alkaline waters of Kuzbass

The first data on abnormally high δ¹³С values in hydrocarbonates (НСО ₃^-) dissolved in underground waters of coal deposits of Kuzbass (up to +30.9‰) are reported. It is shown that such an unusual isotope composition of waters results from the long, strictly directed interaction in the water–rock–gas–organic material system occurring under the conditions of hindered water exchange. Extensive fractionation of C isotopes is the result of the evolution of the water–rock–gas–coal system after penetration of infiltration waters into the coal deposits and their long interaction with all these components, rather than metamorphism of organic material upon its transformation into coal. With respect to such an approach, the isotope composition of dissolved C may indicate the duration of the evolution in the water–rock–gas–organic material system.     

Influence of long-period oscillations on the development of droughts in Northern Eurasia

Doklady Earth Sciences - Estimates of the influence of the Atlantic long-period oscillation (ALO) on the formation of droughts in Northern Eurasia were obtained using the results of numerical...     

Disseminated gold–sulfide mineralization at the Zhaima deposit,eastern Kazakhstan

The Zhaima gold–sulfide deposit is located in the northwestern part of the West Kalba gold belt in eastern Kazakhstan. The mineralization is hosted in Lower Carboniferous volcanic and carbonate rocks formed under conditions of marginal-sea and island-arc volcanic activity. The paper considers the mineralogy and geochemistry of primary gold–sulfide ore and Au-bearing weathering crusts. Au-bearing arsenopyrite–pyrite mineralization formed during only one productive stage. Disseminated, stringer–disseminated, and massive rocks are enriched in Ti, Cr, V, Cu, and Ni, which correspond to the mafic profile of basement. The main ores minerals are represented by finely acicular arsenopyrite containing Au (up to few tens of ppm) and cubic and pentagonal dodecahedral pyrite with sporadic submicroscopic inclusions of native gold. The sulfur isotopic composition of sulfides is close to that of the meteoritic standard (δ³⁴S =–0.2 to +0.2). The ⁴⁰Ar/³⁹Ar age of three sericite samples from ore veinlets corresponds to the Early Permian: 279 ± 3.3, 275.6 ± 2.9, and 272.2 ± 2.9 Ma. The mantle source of sulfur, ore geochemistry, and spatial compatibility of mineralization with basic dikes allow us to speak about the existence of deep fluid–magmatic systems apparently conjugate with the Tarim plume.     

Deposition conditions and distribution features of native gold individuals in the veins of the Tokur mesothermal deposit,Russia

The paper discusses factors in the deposition and concentration of native gold and the spatial distribution of its individuals within the sufide-poor gold–quartz veins at the mesoabyssal Tokur deposit. The major factors in deposition of gold were sealing of the hydrothermal system, a sudden drop in fluid pressure, and repeated immiscibility in the fluid. Native gold was deposited in relation to initial acts of prolonged and discrete opening and preopening of cavities in three mineral assemblages of the productive association II. Most native gold individuals with a visible size of 0.1–1.5 mm were together with the early generation of quartz 2 on cavity walls adjacent to altered rocks. This is caused by the high content of Au complexes in initial hydrothermal solutions favoring rapid oversaturation during cavity formation. Gold fills interstices between grains of quartz 2 throughout the deposit and mineral assemblages. The vertical-flow distribution of gold has been established in economic veins; the upper and middle levels are enriched in gold, and samples with the greatest gold grade of 100–500 g/t or higher are concentrated there. This is caused both by the predominance of mineral association II at these levels and probable natural flotation of gold grains contained in the gold–gas associate for immiscibility of the hydrothermal fluid at the second stage of the ore-forming process.     

Geology and mineralogy of the Alakha spodumene granite porphyry deposit,Gorny Altai,Russia

The Alakha lithium–tantalum deposit in the southern Altai, Russia, is represented by a stock of spodumene-bearing granite porphyry localized in the Kalba–Narym–Koktogai lithium–tantalum rare-metal granitic belt, unique in extent (more than 1000 km). This belt is a part of the Altai accretionary–collisional system. Judging from forecasting, the Alakha deposit can be regarded as an uneroded proxy of a pegmatite body both in dimensions and mean Li₂O and Ta₂O₅ contents (0.98 wt % and 114 ppm, respectively); however, the oregenerating potential of this deposit remains insufficiently studied and had not yet been claimed. In this paper, we attempt to fill this gap with a detailed mineralogical study, which allows us to provide insights into the crystallization of Li-bearing high-silicic magma and redistribution of components during magmatic and postmagmatic processes. Accessory mineral assemblages in muscovite–spodumene–K-feldspar granite porphyry and muscovite albitite—the main petrographic rock varieties of the Alakha stock—turned out to be almost identical. A significant similarity in the chemistry of major rock-forming minerals is established for spodumene granite porphyry of the Alakha stock and spodumene pegmatites from large deposits, which makes it possible to suggest that they are close in the petrogenetic mechanism of their formation. The mineral assemblages of muscovite albitite in the apical portion of the Alakha stock are connected by gradual transition with those of spodumene granite porphyry. Such a transition is caused by postmagmatic metasomatic alteration of the latter.     

IR photometry and models for the dust envelopes of two carbon stars

The results of JHKLM photometry of two carbon stars are presented: the irregular variable NQ Cas and the Mira star BD Vul. Data on the mean fluxes supplemented with mid-IR observations with the IRAS, AKARI, andWISE satellites are used to compute spherically symmetrical model dust envelopes for the stars, consisting of particles of amorphous carbon and silicon carbide. The optical depth in the visible for the comparatively cool dust envelope of BD Vul, with a dust temperature at its inner boundary T₁ = 610 K, is fairly low: τ_V = 0.13. The dust envelope of NQ Cas is appreciably hotter (T₁ = 1550 K), and has τ_V = 0.32. The estimated mass-loss rates are 1.5 × 10^?7M_⊙/yr for NQ Cas and 5.9 × 10^?7M_⊙/yr for BD Vul.     

The Air-Coastal Sea Chemical Exchange: A Case Study on the New Jersey Coast

The coastal marine atmosphere adjacent to large urban and industrial centers is in general strongly impacted by pollution emissions, resulting in high loading of pollutants in the ambient air. Among the airborne substances are certain trace elements from a variety of emission sources that can serve as micronutrients to marine organisms in coastal waters. High concentrations of such elements in coastal air can result in enhanced air-to-sea deposition fluxes to coastal waters. They could also be transported over the open ocean, affecting the composition of the remote marine atmosphere and then ocean ecosystems. To provide better understanding of the extent of air-to-sea deposition processes on the New Jersey coast, a heavily polluted coastal region on the US East Coast, a synthesis of observation data was carried out for selected trace elements, including Fe, Cd, Cr and Cu, derived from measurements of both size-segregated and bulk aerosol particles, as well as precipitation around the New Jersey coast. The atmospheric input of Hg was also estimated based on measurement data. Results indicated that the total deposition fluxes of most trace elements were higher in Northern coastal NJ compared to Southern coastal NJ, reflecting the differences in the source strengths of these element emissions between the two coastal regions. Dry deposition processes were more significant for common dust-derived elements, particularly Fe and Al, compared with their wet deposition fluxes. However, the processes of precipitation scavenging appeared to be more important for the elements that were often enriched in fine particles including Zn, Cu, Pb and Ni. The removal of Hg from the ambient air was overwhelmingly dominated by atmospheric wet deposition. In the future, atmospheric measurements at more sites on the NJ coast should be performed simultaneously to reduce the spatial and temporal uncertainties associated with atmospheric deposition fluxes estimated in this study.     

Marine Chemistry in the Coastal Environment: Principles,Perspective and Prospectus

Marine chemistry of the coastal environment starts with principles of rock weathering that use carbonic acid to mobilize elements, only some of which comprise the majority of sea salt. The principle reason is reverse weathering, extensively represented in coastal waters, and returns most elements to newly formed colloids or minerals while recycling carbon dioxide to the atmosphere. This includes the deeper ocean expanse of sediment diagenesis, plus hydrothermal plumes and attendant low-temperature basalt alteration. Within the estuarine and extended shelf regimes, both conservative and non-conservative processes can be distinguished and modeled to determine proportions of weathered elements transmitted to the sea or consumed by reverse weathering. Conceptually, the steady-state processes that lead to the composition of seawater can be viewed as heterogeneous equilibria between dissolved constituents and solid mineral products taking hundreds of millennia. However, initial processes in the estuarine and coastal environment are characterized by shorter term scavenging associated with inorganic and organic colloids. These recycle both carbon and trace elements on timescales commensurate with estuarine flushing and coastal exchange with the ocean. The natural uranium and thorium decay series provide powerful tools for quantifying the rates of estuarine processes, including those within groundwater and the subterranean estuary. In the future, new mass spectrometric and nuclear magnetic resonance techniques will help to define the molecular nature of newly formed estuarine colloids as has been done for dissolved organic matter. As the coastal environment undergoes the forces of climate change in the form of warming and sea level rise, future research should address how these will impact chemistry of the coastal environment as a net source or sink of carbon dioxide and associated organic material.