长江河口沙坝全新统沉积特征和环境变迁

长江口崇明、长兴、横沙等岛屿是由全新世长江的河口沙坝孕育而成。晚更新世末长江门曾遭受了强烈的侵蚀,古河谷切割甚深。嗣后,在此地质背景上发育了河口沙坝,其全新世沉积相当完整。它们是研究长江河口三角洲形成史和沉积过程的有力证据。笔者着重探讨全新统的沉积环境变迁,旨在为研究长江三角洲发育及其经济区的开发提供地质依据。     

甘肃拾金坡金矿床成因:来自40Ar/39Ar定年、成矿流体及H-O-S同位素证据

甘肃拾金坡金矿床是北山造山带南部的一处重要中型金矿床。矿体以石英脉和蚀变岩形式产出,受东西向断裂控制,赋矿围岩为早泥盆世拾金坡二长花岗岩。矿石中主要金属硫化物为黄铁矿及少量方铅矿、闪锌矿和磁黄铁矿。石英脉两侧花岗岩发生强烈的硅化、黄铁绢英岩化和绿泥石化。热液蚀变绢云母40 Ar/39 Ar坪年龄为(364.6±3)Ma,表明成矿作用发生在晚泥盆世。矿石石英中流体包裹体可分为早晚两期:早期流体包裹体群包含不同气液比水溶液包裹体和含CO2包裹体,指示成矿过程存在流体沸腾作用,其均一温度集中在280～325℃,盐度(w(NaCl))为7.86%～9.21%;晚期流体包裹体群只发育水溶液包裹体,均一温度集中于160～230℃,盐度为9.47%～11.10%。成矿流体属中温低盐度、富CO2流体。流体从早阶段演化到晚阶段,温度降低约100℃,压力由约113 MPa骤减到约11 MPa。流体包裹体的δ18 OH2O值为1.39‰～3.39‰,δD值为-71‰～-99‰。氢氧投图中,石英脉和蚀变岩样品构成良好的线性关系,暗示初始成矿流体主要来自变质热液,晚期有强烈大气降水加入。矿石金属硫化物δ34S值变化范围为4.44‰～11.33‰,峰值为8‰～9‰,呈塔式分布。与区域S同位素资料对比分析表明,石英脉型矿石S主要来自前寒武系基底,蚀变岩型矿石S更多地继承了花岗岩围岩S。综合分析认为,拾金坡金矿床属于造山型金矿,形成于造山晚期挤压—伸展转换环境。     

特厚砂土层条件下的开采沉陷规律研究

在分析榆树湾煤矿地表移动观测资料的基础上,研究了特厚砂土层条件下的厚煤层开采的地表移动变形规律与特征。揭示了特厚砂土层、薄基岩及大采厚等特殊因素对地表沉陷规律的影响,获得了特厚砂土层开采条件下的地表移动变形特征,研究成果将对榆林煤矿后续的安全合理开采、保安煤柱的留设、环境治理与保护等具有重要的实际意义。     

Geochemical Characteristics of Different Kinds of Crude Oils in the Tarim Basin,Northwest China

Based on the compositions and distributions of biomarkers in thirty-five representative oil samples, oils from the Tarim Basin of northwestern China are mainly divided into two oil families. One oil family contains relatively low amounts of C₁₅-C₂₀ isoprenoid hydrocarbons and shows pristane predominance with Pr/Ph ratios ranging from 1.50 to 3.00. The GC/MS analytical data of these oils show the occurrence of abundant hopanes, and low concentrations of steranes and tricyclic terpanes with hopanes/steranes ratios from 6.25 to 12.24 and tricyclic terpanes/hopanes ratios from 0.03 to 0.24. These oils contain low drimane relative to homodrimane (C₁₅/C₁₆ < 1.0) and abundant rearranged bicyclanes in bicyclic sesquiterpanes. They are dominated by low carbon number (C₁₉-C₂₁) compounds in the tricyclic terpanes, and are rich in rearranged hopanes, C₂₉Ts and an unknown C₃₀ compound in pentacyclic triterpanes. These geochemical characteristics suggest that the oils were generated mainly from terrigenous organic matter. The other oil family shows remarkably different biomarker compositions and distributions. The oils revealed Pr/Ph ratios of about 1.0, high drimane/homodrimane ratios (>1.0), low hopanes/steranes ratios (0.65–2.50), high tricyclic terpanes/hopanes ratios (0.30–2.00) and a dominant peak at C₂₃ in tricyclic tepanes, suggesting a marine organic origin. Oil-source rock correlation indicates that these two oil families seem to have been derived from Mesozoic Jurassic-Triassic terrestrial source rocks (shales and coal seams) and Lower Paleozoic Ordovician-Cambrian marine source rocks, respectively.     

Compositional fractionation of polyaromatic hydrocarbons in the karst soils, South China

This study aims to explore the condensation and fractionation trends of persistent organic pollutants (POPs) in the karst soils. The tiankeng is a karst surface expression that can act as a focal point for introduction of contaminants to a karst aquifer, which may serve both as condenser for vapor phase POPs and as barrier/sink for particulate associated less volatile POPs. The fractionation of POPs in soils from the upper rim and floor of tiankeng is of interest in understanding the role of tiankeng in the long-distance transport of POPs. In the present study, polycyclic aromatic hydrocarbons (PAHs) in the surface soils from the upper rim and floor of Dashiwei tiankeng in Southern China were analyzed. The total PAH concentrations in soils were 23.40–190 ng g⁻¹, with phenanthrene being the most abundant. The distribution patterns of PAH compounds in the soil samples matched well with their properties. It indicated the heavy PAHs were susceptible to retention by the floor soils of tiankeng than light PAHs. A plot of Cfloor/Crim against PAH molecular weight gave a good positive relationship in the molecular weight range of 152–276. It is suggested that the floor soils can be focal points of more concentrated PAH and deserve attention. The concentrations of total PAHs in the floor soils (43.40–190 ng g⁻¹, mean 87.76 ng g⁻¹) were higher than those in the upper rim (23.40–88.94 ng g⁻¹, mean 57.74 ng g⁻¹). In addition, there was a shift in compound pattern with an increase in the proportion of light PAHs (2–3 rings), a decrease in heavy PAHs (5–6 rings) and a relatively stable content of 4-ring PAHs. A combination of particulate scavenging and cold condensation is proposed as the major mechanism for the compositional fractionation of PAHs in the soils from the upper rim and floor of tiankeng.     

Gneiss-Water Interaction and Water Evolution During the Early Stages of Dissolution Experiments at Room Temperature

Gneiss-distilled water interaction at room temperature was investigated with batch-reactors to study water-rock reaction and geochemical evolution of the aqueous phase with time. The ion concentrations in water were controlled not only by the dissolution of primary minerals, but also by the precipitation of secondary minerals. The decreasing fraction sizes of gneiss could favor dissolution and precipitation simultaneously. Ca^2 and K^ were the major cations, and HCO3^- was the major anion in water. All the ions except Ca^2 increased in concentration with time. The Ca^2 release from the rock to the aqueous phase was initially much faster than the release of K^ , Na^2 and Mg^2 . But after about 5 - 24 hours, the Ca^2 concentrations in water decreased very slowly with time and became relatively stable. During the experiment, the water varied from the Ca-( K)-HCO3-type water to the K-Ca-HCO3-type water, and then to the K-(Ca, Na)-HCO3-type water. The water-gneiss interaction was dominated by the dissolution of Kfeldspar in the solution. The remaining secondary minerals were mainly kaolinite, illite and K (Mg) -mica.     

激发极化弛豫时间谱测井仪探测特性理论分析

大庆测井公司提出具有自主知识产权的激发极化弛豫时间谱测井方法,并研制出了仪器原理样机。这里利用数值分析技术计算了仪器的探测特性。对于仪器分辨率,以简化井眼模型为基础,利用格林函数得出了仪器层厚响应的计算公式,并将计算结果与自然电位测井层厚响应对比,给出仪器的定性分辨率为0．4m;对于仪器的探测深度,利用有限元数值模拟方法得到地层中电位分布,并与核磁共振仪器相类比,得出仪器探测深度为0．75m。     

从第二次土地调查看上海市地籍管理

本文分析了上海市第二次土地调查中地籍调查的技术方法,结合上海市地籍管理现状,根据实际工作需要,提出改进和完善地籍管理的几点思考。     

Erratum to: Iron isotope variations in spinel peridotite xenoliths from North China Craton: implications for mantle metasomatism

Iron isotopes, together with mineral elemental compositions of spinel peridotite xenoliths and clinopyroxenites from Hannuoba and Hebi Cenozoic alkaline basalts, were analyzed to investigate iron isotopic features of the lithospheric mantle beneath the North China Craton. The results show that the Hannuoba spinel peridotite xenoliths have small but distinguishable Fe isotopic variations. Overall variations in δ⁵⁷Fe are in a range of −0.25 to 0.14‰ for olivine, −0.17 to 0.17‰ for orthopyroxene, −0.21 to 0.27‰ for clinopyroxene, and −0.16 to 0.26‰ for spinel, respectively. Clinopyroxene has the heaviest iron isotopic ratio and olivine the lightest within individual sample. No clear linear relationships between the mineral pairs on “δ-δ” plot suggest that iron isotopes of mineral separates analyzed have been affected largely by some open system processes. The broadly negative correlations between mineral iron isotopes and metasomatic indexes such as spinel Cr#, (La/Yb)_N ratios of clinopyroxenes suggest that iron isotopic variations in different minerals and peridotites were probably produced by mantle metasomatism. The Hebi phlogopite-bearing lherzolite, which is significantly modified by metasomatic events, appears to be much heavier isotopically than clinopyroxene-poor lherzolite. This study further confirms previous conclusions that the lithospheric mantle has distinguishable and heterogeneous iron isotopic variations at the xenoliths scale. Mantle metasomatism is the most likely cause for the iron isotope variations in mantle peridotites.     

静电场轨道阱质谱在水中溶解性有机质表征中的应用进展

溶解性有机质(Dissolved Organic Matter,DOM)在水生生态环境中广泛存在,影响着水环境中多种物质的生物地球化学性质.分析其组成与含量具有重要的生态环境意义,是生态环境科学领域研究的热点.溶解性有机质组成非常复杂,其分子组成的解析一直是难题.近年来,具有高分辨率、高灵敏度、高通量、高扫描速率等特性...