Vol 55, No 12 (2017)

Hainan Island lies at the southern tip of the South China block that was affected by the opening and closure of the paleo-Tethys from Paleozoic to Mesozoic and subsequently by the subduction of the paleo- Pacific plate beneath the Euroasian plate since the late Mesozoic era. This study presents zircon U-Pb ages and geochemistry of granites and basic diabase veins in Dazhou Island located 5 km southeast of Hainan Island. The age for granites is 237.2 Ma (MSWD = 0.14, n = 14), suggesting that they were emplaced in the late middle Triassic and are products of magmatic-tectonic episodes during the closure of paleo-Tethys. The granites belong to the shoshonitic magmatic series and are metaluminous I-type granites. They are systematically depleted in Ba, Nb, Sr, P, and Ti, and have variable ranges of initial ⁸⁷Sr/⁸⁶Sr ratios (0.71005 ~ 0.71110), but relatively constant εNd(t) values (–6.4~–6.8). The two-stage depleted mantle Nd model ages (T_DM2 = 1531–1562 Ma) for these granites suggest that they may have originated from partial melting of the lower crust with a crustal residence age of early Middle Proterozoic Era. The zircon U-Pb ages for diabase veins can be divided into three groups. The age for Group I is 236.8 Ma (n = 4), which represents the crystallization age of the veins and somewhat younger than the accompanying granites. The ages for Group II and III are 1767 Ma (n = 6) and 2432 Ma (n = 3), respectively. These suggest that the veins have inherited some old zircons that possibly represent old geological events in the Hainan Islands. The diabase also belongs to the shoshonitic magmatic series and has arc-like trace element characteristics. The veins have high 87Sr/86Sr and low 143Nd/144Nd ratios, which suggest that they may have originated from an enriched mantle II type source or a mantle source metasomatized by aqueous fluids released from previously subducted slab. The new ages obtained for the Dazhou igneous rocks in the present study are similar to those for the Qiongzhong batholith in the Hainan Island, which implies that the Hainan Island had also regionally experienced a middle Triassic extension event after the Indosinian Orogeny.

The paper presents chromatographic–mass spectrometric data on the individual composition of organic compounds in sapropel-like deposits of lakes in the steppe, forest–steppe, and three taiga natural climatic zones (NCZ) in Khakassia and western Siberia. Data on the individual composition of n-alkanes, carboxylic acids and their esters, thiophenes, phytol, phytone, steroids, and di- and triterpenoids and on their distribution in the sediments show systematic variations in the composition of the organic matter (OM) with increasing ambient temperature and the aridity of the climate. The concentrations of all groups of the compounds in lacustrine sediments decrease southward, and simultaneously esters with long (up to С₂₀) alkyl substituents appear. The concentrations of oxygen-bearing compounds increase among the acyclic structures and triterpenoids, as also do the concentrations of structures ketonic substituents among the steroids. The dominance of the carboxylic acids and their esters by high molecular weight homologues gives way to the dominance of palmic acid and its derivatives. Among n-alkanes, the dominance of С₂₇ and С₂₉ hydrocarbons typical of terrestrial plants gives way to a higher percentage of homologues С₂₁–С₂₅ (macrophytes) and С₃₁ (herbaceous plants). Among the tocopheroles, the concentration of the oxidized form of α-tocopherol (acetate) increases.

Thermodynamic numerical simulations were carried out to determine the principal simple and complex migration species of Ca, Mg, Na, K, Al, B, Mn, Mo, Sr, and U with Cl^–, OH^–, SO₄⁻², HCO₃⁻, and CO₃²⁻ in waters at the Lomonosov diamond deposit and to estimate the saturation indexes with respect to kaolinite, Na- and Mg-montmorillonite, Mg- and Na-saponite, muscovite and paragonite, biotite, phlogopite, chromite, pyrite, plagioclase (anorthite, labradorite, and andesine), olivine (forsterite and fayalite), diopside, pyrope, gypsum, anhydrite, barite, magnesite, calcite, dolomite, talc, chrysotile, chlorite, goethite, quartz, microcline, and albite. The waters are proved not to be saturated with respect to the primary (hydrothermal) minerals. The saturation of certain water samples with uranophane suggests that this mineral is of secondary genesis. The ascent of highly mineralized deep waters shall result in the dissolution of minerals whose concentrations are near the saturation ones. To maintain the ecological standards of the discharged waters, they should be diluted and/or purified by adsorbing dissolved U on a reducing reactive barrier.

The lower part of Shayi Member (Es1x Sub-Member) composed mainly of dark mudstones and shales is the dominant source rocks for the Lixian Slope. Based on organic petrology, organic and inorganic geochemistry analyses of several mudstone and shale samples selected from Es1x Sub-Member, this research provides an overview on type, origin and thermal maturity of organic matters, as well as depositional environment of Es1x Sub-Member. Kerogen microscopy observation shows that the macerals are dominated by sapropelinite with a significant mixture of vitrinite and inertinite, indicating that aquatic algal-bacterial organic matter inputs are dominate with a significant contribution of terrigenous organic matter inputs. This statement is supported by n-alkane patterns distribution characteristics, high (n-C₂₁ + n-C₂₂)/(n-C₂₈ + n-C₂₉) values (average = 1.77), the plot of high Ph/n-C₁₈ values (average = 4.15) versus low Pr/n-C₁₇ values (average = 1.13), and high proportion of C₂₇ sterane and C₂₉ sterane (average = 37.7 and 42.0%, respectively). In addition, the rather low Pr/Ph values (average = 0.38), high gammacerane index values (average = 0.30), high V/Ni and V/(V + Ni) values (average = 11.84 and 0.89, respectively), high Sr/Ba and Sr/Cu values (average = 8.54 and 108, respectively), indicative of a saline water condition and a anoxic depositional environment. The low C29 sterane ααα 20S/(20S + 20R), C₂₉ sterane αββ/(αββ + ααα), C₃₁ homohopane 22S/(22S + 22R), C₃₂ homohopane 22S/(22S + 22R), Ts/(Ts + Tm) values and relatively high moretane/hopane values show that the level of thermal maturity of organic matters in Es1x Sub-Member are low.

Hydrogeochemical background determined for an investigated environment, defines characteristic range of its hydrochemical characteristics. This allows to observe the temporal changes of the chemical water properties taking place in the studied environments, such as due to human impact. The paper presents the results of study on the present-day hydrogeochemical background in the Lubuskie Lakeland, the region repeatedly covered by the ice sheets during the Pleistocene and little affected by anthropogenic impact. The hydrogeochemical background was established on a basis of physicochemical analyses of spring waters sampled every 3 months between November 2011 and October 2013 from 20 springs. Present-day hydrogeochemical background was assumed to be represented by values ranging between 16 and 84 percentiles. The ranges of hydrogeochemical background for the studied ions on the Lubuskie Lakeland, were in the lower range of the background considered for useful waters in Poland. The obtained results indicated that the studied spring waters were poorly diversified in terms of composition of main cations and anions, as well as electrical conductivity and total water hardness. However, large variability was observed for Fe_tot, Mn²⁺ and NO₃⁻. Moreover, NO₃⁻ and SO₄²⁻ were noted in some cases to be in excess of national hydrogeochemical background values.

Major, trace and rare earth elements (REE) concentration of the Eocene limestones, Jaisalmer Basin, Rajasthan, India are analysed to reconstruct the depositional conditions and to identify sources of REEs. Among the major oxides, CaO is the dominant oxide followed by SiO₂ in the studied limestones. Trace element Ba dominates over the other trace elements and it shows negative correlation with CaO. The Sr, occurring in small concentration, shows positive correlation with CaO. Other trace elements such as V, Zr, Sc, Y, Rb, Ni, Pb Co, Cu, U occur in small concentrations. The studied limestones show a positive correlation of ΣREE with Fe₂O₃, Ni, Th, Sc, and Y. These limestones possess sea-water like shale-normalized REE + Y pattern with light REE depletion, slight Gd enrichment, slightly positive La anomaly, positive Y anomaly, positive Eu anomaly, negative Ce anomaly and superchondritic Y/Ho ratio from 23.12 to 28.57. The dominance of CaO and low percentage of MgO suggest that mineral phase is calcite and there is absence of dolomitization. The occurrence of SiO₂ and Al₂O₃ in appreciable percentages may be because of the siliciclastic input during the limestone precipiatetion. The low concentration of Uranium (0.4-3.7) and authigenic Uranium (Average Total U-Th/3 value = 0.74) indicate that the studied limestones were precipitated in oxic condition from seawater. The depletion of LREE suggests that the limestones were precipitated from the seawater. The positive correlation of ΣREE with Al₂O₃ Fe₂O₃, Ni, Th, Sc, and Y and negative correlation with CaO suggest an input of siliciclastic sediments from the land during limestone precipitation. The negative Ce anomaly, slightly positive La anomaly, slight Gd enrichment, positive Y anomaly, and positive Eu anomaly also suggest that the limestone was precipitated from the seawater with some siliciclastic input from continent. The low values of the Y/Ho ratio (23.12 to 28.57) in the studied limestones suggest some modification of the seawater by the input of freshwater in a coastal environment. The REEs of the studied limestones are correlable with the shallow sea water REEs with exception of a few elements. We envisage a coastal/shallow marine depositional environment where mixing of the continental material in sea water appears feasible.