Traces of structural H2O molecules in baryte

The infrared (IR) spectra of gem-quality baryte crystals from different occurrences are characterized by relatively weak but strongly pleochroic absorption bands at 3,280, 3,220, 3,155, and 3,115 cm⁻¹. These bands are assigned to anti-symmetric and symmetric OH stretching vibrations of two types of H₂O molecules localized on vacant Ba sites. The H–H axis of the H₂O I molecule is slightly tilted from the a-axis direction, its twofold axis being nearly parallel to the b-axis, thus defining the plane of the H₂O molecule practically parallel to (001). The H₂O II molecule has its H–H axis parallel to the b-axis direction, with its plane lying approximately parallel to (101). The values of the total water contents of the baryte crystals, calculated on the basis of IR spectroscopic data, are ranging from about 1.7–3.8 wt.ppm. The possible presence of H₃O⁺ ions is also discussed.     

Trace-element study and uranium-lead dating of perovskite from the Afrikanda plutonic complex, Kola Peninsula (Russia) using LA-ICP-MS

The U-Pb geochronology of perovskite is a powerful tool in constraining the emplacement age of silica-undersaturated rocks. The trace-element and U-Pb isotopic compositions of perovskite from clinopyroxenite and silicocarbonatite from the Afrikanda plutonic complex (Kola, Russia) were determined by laser-ablation inductively-coupled mass-spectrometry (LA-ICP-MS). In addition, the Sr isotopic composition of perovskite was measured by isotope-dilution mass-spectrometry to better constrain the relations between its host rocks. Perovskite from the two rock types shows a different degree of enrichment in Na, Mg, Mn, Pb, Fe, Al, V, rare-earth elements, Zr, Hf, Th, U and Ta. The perovskite ⁸⁷Sr/⁸⁶Sr values are within analytical uncertainty of one another and fall within the range of mantle values. The ²⁰⁶Pb/²³⁸U ages (corrected for common lead using ²⁰⁷Pb-method) of perovskite from silicocarbonatite statistically yield a single population with a weighted mean of 371?±?8 Ma (2σ; MSWD?=?0.071). This age is indistinguishable, within uncertainty, to the clinopyroxenite weighted mean ²⁰⁶Pb/²³⁸U age of 374?±?10 Ma (2σ; MSWD?=?0.18). Our data are in good agreement with the previous geochronological study of the Afrikanda complex. The observed variations in trace-element composition of perovskite from silicocarbonatite and clinopyroxenite indicate that these rocks are not related by crystal fractionation. The Sr isotopic ratios and the fact that the two rocks are coeval suggest that they were either produced from a single parental melt by liquid immiscibility, or from two separate magmas derived at different degrees of partial melting from an isotopically equilibrated, but modally complex mantle source.     

岩性油藏地震描述技术在准噶尔盆地春光油田的应用

准噶尔盆地春光油田新近系沙湾组岩性油藏埋藏浅、厚度薄、成岩作用差,勘探效果不理想。利用层拉平切片技术确定有利储集相带、分频技术雕刻砂体、"类亮点"特征检测流体、进一步采用拟声波+电阻率反演两步法鉴别流体,这一技术方法系列在春光油田的实际应用效果良好。用拟声波+电阻率反演两步法可以检测出无亮点特征的含油砂体或含水砂体。对于不具备"类亮点"特征的滩坝砂油藏的勘探,可由原来的应用"类亮点"特征直接找油转为寻找有效圈闭,并在此基础上应用合适的流体检测技术,这同样可以发现有利的滩坝砂油藏。     

Contamination levels assessment of potential toxic metals in road dust deposited in different types of urban environment

A total of 42 samples of road dust were collected along ring road, city centre, city side, and freeway in Urumqi, China. Total concentrations of Cd, Cr, Cu, Ni, Pb, Mn, Be, Co, Zn, and U were determined by using the inductively coupled plasma-mass spectrometry in order to assess and to compare road dust contamination levels of metals among the four roads. The results show that, among the four categories of roads, mean concentrations of Co and U vary little. City centre locations show strong enrichments of Cd, Cu, Pb, and Be. Along the ring road, the highest mean concentrations were found for Cr, Ni, Mn, and Co. However, the highest concentrations of Zn and U were found along the freeway. The cluster analysis shows that three main groups can be distinguished. Every group may be associated with different main sources and concentrations of the metals. The results of contamination assessment reveal that, among all of the potential toxic metals, Cd, Cu, and Zn pollution were obviously heavier with moderate or high contamination indices for most road dust samples, while Cr, Ni, and Pb contamination were lower along the four categories of roads. Compared with the city side, Cd, Cu, Pb, Ni, and Zn contamination were heavier along the ring road, the city centre, and the freeway with high traffic density. Low Pb contamination or no contamination in all the road dust samples may be related to the increasing usage of lead-free petrol.     

XX核电厂附近海域生态环境及潜在致灾生物研究

为了了解XX核电厂周边海域的生态环境状况,筛选潜在威胁核电厂冷源安全的致灾生物,分析影响致灾生物时空分布的主要环境因素,本研究于2018年进行了四个季节的生态调查。结果表明,研究海域浮游植物密度秋季最高,春季优势种为东海原甲藻,其他季节优势种为中肋骨条藻等硅藻。浮游动物密度夏季最高,以桡足类为主,春、夏季优势种还包括球型侧腕水母和薮枝螅水母。底栖动物的密度和生物量在秋季最高,优势种主要为豆形短眼蟹、长吻沙蚕和丝异须虫。浮游植物、浮游动物和底栖动物群落均在夏季最为稳定,群落多样性水平和物种丰度较高,且分布较为均匀。浮游植物群落的细胞丰度与悬浮物和磷酸盐的浓度正相关性最高。浮游动物的密度受温度和盐度的影响较大。底栖动物的群落分布主要受悬浮物和无机营养盐的浓度影响。本研究共筛选出17种威胁XX核电厂冷源安全的潜在致灾生物。海地瓜、棘刺锚参、海葵和球型侧腕水母的风险等级较高,其分布主要受温度和盐度的影响。后续工作中,XX核电厂应根据潜在致灾生物与环境因子的关系加强暴发机制研究、提升监测预警能力,并优化驱赶消杀技术和干扰体系,为核电厂冷源安全提供理论和技术保障。     

Soil and vegetation seasonal changes in the grazing Andean Mountain grasslands

Andean grasslands ecosystems are fragile environments with rigorous climatologic conditions and low and variable food for the grazing. The Apolobamba area is located in the Bolivian Andean Mountains. Its high grasslands provide a natural habitat for wild and domestic camelids such as vicuna（Vicugna vicugna） and alpaca（Lama pacos）. The botanical diversity plays an essential role in maintaining vital ecosystem functions. The objectives of this research were to determine the seasonal changes in soil properties, to study the vegetation changes during the wet and dry seasons and the influence of soil properties and camelid densities on the vegetation in the Apolobamba grasslands. Four zones with different vicuna populations were selected to be studied. The following soil parameters were determined： total organic carbon, total nitrogen, available phosphorous, cation exchange capacity, exchangeable cations, pH and texture. The vegetation season changes were studied through botanical identification, above-ground biomass, plant cover and species richness. Results showed that some soil properties such as C/N ratio, CEC, silt and clay percentages kept stable against the seasonal changes. Generally, soil nutrients were relatively higher during the dry season in the surface and subsurface. The results did not point out the predominant vegetation growth during the wet season. The seasonal vegetation growth depended on each species. Thegood soil fertility corresponded to the highest plant cover. Soil fertility presented no influence on the above-ground biomass of the collected species. The negative influence of camelid grazing on soil properties could not be assessed. However, overgrazing could affect some plant species. Therefore, protection is needed in order to preserve the biodiversity in the Andean mountain grasslands.     

Dissolution–precipitation processes governing the carbonation and silicification of the serpentinite sole of the New Caledonia ophiolite

The weathering of mantle peridotite tectonically exposed to the atmosphere leads commonly to natural carbonation processes. Extensive cryptocrystalline magnesite veins and stock-work are widespread in the serpentinite sole of the New Caledonia ophiolite. Silica is systematically associated with magnesite. It is commonly admitted that Mg and Si are released during the laterization of overlying peridotites. Thus, the occurrence of these veins is generally attributed to a per descensum mechanism that involves the infiltration of meteoric waters enriched in dissolved atmospheric CO₂. In this study, we investigate serpentinite carbonation processes, and related silicification, based on a detailed petrographic and crystal chemical study of serpentinites. The relationships between serpentine and alteration products are described using an original method for the analysis of micro-X-ray fluorescence images performed at the centimeter scale. Our investigations highlight a carbonation mechanism, together with precipitation of amorphous silica and sepiolite, based on a dissolution–precipitation process. In contrast with the per descensum Mg/Si-enrichment model that is mainly concentrated in rock fractures, dissolution–precipitation process is much more pervasive. Thus, although the texture of rocks remains relatively preserved, this process extends more widely into the rock and may represent a major part of total carbonation of the ophiolite.     

Observations on the crystal structures of lueshite

Laboratory powder XRD patterns of the perovskite-group mineral lueshite from the type locality (Lueshe, Kivu, DRC) and pure NaNbO₃ demonstrate that lueshite does not adopt the same space group (Pbma; #57) as the synthetic compound. The crystal structures of lueshite (2 samples) from Lueshe, Mont Saint-Hilaire (Quebec, Canada) and Sallanlatvi (Kola, Russia) have been determined by single-crystal CCD X-ray diffraction. These room temperature X-ray data for all single-crystal samples can be satisfactorily refined in the orthorhombic space group Pbnm (#62). Cell dimensions, atomic coordinates of the atoms, bond lengths and octahedron tilt angles are given for four crystals. Conventional neutron diffraction patterns for Lueshe lueshite recorded over the temperature range 11–1,000 K confirm that lueshite does not adopt space group Pbma within these temperatures. Neutron diffraction indicates no phase changes on cooling from room temperature to 11 K. None of these neutron diffraction data give satisfactorily refinements but suggest that this is the space group Pbnm. Time-of-flight neutron diffraction patterns for Lueshe lueshite recorded from room temperature to 700 °C demonstrate phase transitions above 550 °C from Cmcm through P4/mbm to \(Pm\overline{3} m\) above 650 °C. Cell dimensions and atomic coordinates of the atoms are given for the three high-temperature phases. The room temperature to 400 °C structures cannot be satisfactorily resolved, and it is suggested that the lueshite at room temperature consists of domains of pinned metastable phases with orthorhombic and/or monoclinic structures. However, the sequence of high-temperature phase transitions observed is similar to those determined for synthetic NaTaO₃, suggesting that the equilibrated room temperature structure of lueshite is orthorhombic Pbnm.