内蒙古苏莫查干敖包特大型萤石矿床地质特征及成因

苏莫查干敖包矿床是迄今为正在全球范围内找到的最大规模单一萤石矿床.萤石矿体大多呈层状、似层状和透镜状沿下二叠统碳泥质板岩(夹灰岩透镜体)与流纹质火山岩接触带分布,并且与中生代花岗岩类侵入岩体具有密切的空间分布关系.流纹质火山岩和花岗岩的锆石SHRIMP U-Pb年龄值分别为(276±10)Ma和(138±4)Ma,它们分别是海西晚期和燕山中期酸性岩浆活动的产物.萤石矿体主要由4种类型矿石所构成,即石英-萤石型、石英-硫化物-萤石型、萤石-石英型和方解石-石英-萤石型.矿物组分有萤石、石英(蛋白石、玉髓)、方解石、绢云母和绿泥石,个别样品中有磁铁矿、黄铁矿、磁黄铁矿、黄铜矿、闪锌矿、毒砂和锡石.围岩蚀变自矿体中心向外分别为绢云母化、硅化、碳酸盐化和高岭石化.钕、锶和铅同位素分析结果表明,萤石矿床是多期次和多阶段岩浆热液活动的产物,成矿作用分别发生在海西晚期和燕山中期,并以后者为主.海西晚期富碱质酸性岩浆喷发活动为层纹状和条带状矿体以及矿源层的形成创造了有利条件.相比之下,燕山中期花岗质岩浆侵入活动不仅为细晶质、伟晶质和角砾状矿体的形成提供了物质、动力和热力来源,而且是成矿流体对流循环的"发动机".苏莫查干敖包矿床属于与花岗岩类深成侵入岩体有关的热液型萤石矿床,成岩(矿)物质来自壳、幔混合源,其中壳源组分占有绝对优势.     

内蒙古敖包吐萤石矿床的Sr、Nd、Pb同位素地球化学特征

敖包吐萤石矿床是内蒙古北部苏莫查干地区单一萤石矿集区中的一个代表性矿床,产于早二叠世大石寨组火山-沉积岩与早白垩世敖包吐花岗岩的接触带上。文章通过分析该矿床岩、矿石的微量元素和稀土元素,揭示出萤石的成矿作用可分为2个阶段,即交代作用和充填作用。交代作用过程中大石寨组的结晶灰岩可能为萤石的形成提供了部分Ca来源,萤石矿石的稀土元素配分模式与海水基本类似,具有Ce负异常;成矿作用后期主要表现为充填作用,形成颗粒粗大的萤石,表现为重稀土元素富集的特征,并随着萤石的沉淀析出,稀土元素总量逐渐下降,反映出成矿流体经历了较长期的演化过程。各地层单元、花岗岩体和萤石矿石的Sr、Nd、Pb同位素研究表明,萤石的放射性同位素组成具有壳、幔源混合的特点,成矿物质来源具有多源性。早白垩世敖包吐花岗岩可能是萤石中F的主要来源,而大石寨组的结晶灰岩则可能提供了Ca。另外,Pb、Nd同位素的极大不均一性,有可能是成矿流体在运移过程中对艾力格庙群放射性组分的选择性吸收的结果。萤石成矿作用与钾玄岩的时空关系暗示了萤石的成矿过程可能是中国东部岩石圈减薄和下地壳的置换地质事件的结果。在构造转型的过程中,燕山中期富碱的酸性花岗岩浆的活动分异出富含F的成矿流体,与幔源流体混合,沿区域重新活化的深大断裂和大石寨组的层间破碎带上升,交代其间的灰岩透镜体,从而形成敖包吐中型萤石矿床。     

柴达木盆地北缘侏罗系不同沉积环境烃源岩生物标志物特征及其应用

柴达木盆地北缘地区侏罗系(中下侏罗统)的优质烃源岩主要发育于湖相与三角洲相环境。研究了不同时代、不同沉积环境中烃源岩的生物标志物组成特征,结果发现,有3类化合物的分布与组成差异显著,包括三环萜烷(C19、C20、C21)的分布型式、重排藿烷的丰度以及规则甾烷的相对组成。其中,不同时代的差异主要体现在规则甾烷组成上;而不同沉积环境的差异主要体现为三环萜烷(C19、C20、C21)的分布型式及重排藿烷的丰度。分析认为,这些差异与烃源岩的沉积环境及其生源组成有密切关系。据此,初步将这些参数应用于两方面研究,一是为划分地层沉积环境提供“生物标志物相标志”,二是研究油源对比,取得良好效果。因此,本文研究结果具有重要实用价值与参考意义。     

An experimental study of the grain-scale processes of peridotite melting: implications for major and trace element distribution during equilibrium and disequilibrium melting

The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar P–T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Simple models for dynamic melting in an upwelling heterogeneous mantle column: Analytical solutions

Several lines of evidence suggest that the melt generation and segregation regions of the mantle are heterogeneous, consisting of chemically and lithologically distinct domains of variable size and dimension. Partial melting of such heterogeneous mantle source regions gives rise to a diverse range of basaltic magmas. In order to better assess the role of source heterogeneity during mantle melting, we have undertaken a theoretical study of trace element distribution and fractionation during concurrent melting and melt migration in an upwelling, chemically heterogeneous, two-porosity double lithology melting column. Analytical solutions for the abundance of a trace element in the matrix and channel were obtained under the assumptions that the porosity, melt and solid velocities, and solid-melt partition coefficients are constant and uniform. For simplicity, we neglected diffusion and dispersion in the melt. Chemical source heterogeneities of arbitrary size and shape were integrated into the simple melting models by allowing trace element abundance in the source region to vary as a function of time and space. Concurrent melting and melt migration in an upwelling heterogeneous mantle may be approximated as a quasi-steady state problem in which time-dependent concentration patterns produced by melting of heterogeneous source regions are superimposed on a reference steady-state concentration distribution established by melting of the ambient or background mantle. Chromatographic fractionation is especially important for the matrix melt and solid when chemical heterogeneities are involved during melting and melt migration in the mantle, giving rise to significant phase-shift between two incompatible trace elements in the matrix melt and scattered correlations among incompatible trace elements in residual peridotites. Mixing is the chief mass transfer process in the dunite channel where the chromatographic effect is negligible for most of the incompatible trace elements. The lack of chromatographic fractionation among incompatible trace elements and isotopic ratios in MORB suggests either most MORB are channel melts or mixing in magma conduit and chamber is very efficient such that the phase-shift is averaged out during magma transport and storage processes. Advection brings melt produced by smaller-degree of melting in the deeper part of the melting column to the overlying melting region, increasing the incompatible trace element abundance in the matrix and the channel. This advection-induced self-enrichment is especially important when heterogeneous sources are involved and may account for some of the enriched incompatible trace element patterns observed in residual peridotite that were previously interpreted to be a result of mantle metasomatism. Systematic studies of high-resolution spatially correlated mantle samples may help to constrain the melting history and the size and nature of chemical heterogeneities in the mantle.     

Considerations for conducting incubations to study the mechanisms of As release in reducing groundwater aquifers

Microbial Fe reduction is widely believed to be the primary mechanism of As release from aquifer sands in Bangladesh, but alternative explanations have been proposed. Long-term incubation studies using natural aquifer material are one way to address such divergent views. This study addresses two issues related to this approach: (1) the need for suitable abiotic controls and (2) the spatial variability of the composition of aquifer sands. Four sterilization techniques were examined using orange-colored Pleistocene sediment from Bangladesh and artificial groundwater over 8 months. Acetate (10 mM) was added to sacrificial vials before sterilization using either (1) 25 kGy of gamma irradiation, (2) three 1-h autoclave cycles, (3) a single addition of an antibiotic mixture at 1× or (4) 10× the typical dose, and (5) a 10 mM addition of azide. The effectiveness of sterilization was evaluated using two indicators of microbial Fe reduction, changes in diffuse spectral reflectance and leachable Fe(II)/Fe ratios, as well as changes in P-extractable As concentrations in the solid phase. A low dose of antibiotics was ineffective after 70 days, whereas autoclaving significantly altered groundwater composition. Gamma irradiation, a high dose of antibiotics, and azide were effective for the duration of the experiment.     

树木年轮重建阿勒泰西部1481-2004年6-9月降水量序列

根据采自阿勒泰西部地区5个采点的树木年轮样本, 建立了该地区的树轮年表. 通过相关普查发现, 其差值年表序列与该地区当年6-9月的降水量存在明显的负相关关系, 且具有明确的树木生理学意义. 用沙勒哈(t, t 1)两个树轮差值年表序列可较好地重建该地区1481-2004年524 a来的当年6-9月的降水量, 且经过交叉检验表明重建方程稳定可靠. 分析发现, 阿勒泰西部地区524 a来的重建降水量序列具有9个偏干阶段和9个偏湿阶段, 并且具有34.8 a、 5.0～5.1 a、 4.3～4.4 a、 3.9～4.0 a、 3.7 a和3.4 a的显著干湿变化准周期. 重建降水量序列在1518年、 1548年、 1634年、 1765年、 1856年前后发生过突变.     

青藏高原中、东部局地因素对地温的双重影响(Ⅰ): 植被和雪盖

青藏高原冻土区地温既受海拔、纬度和经度(干燥度)区域地带性规律控制, 同时它又受植被、雪盖、砂层、 水被和地质构造等局地因素的显著影响. 局地因素对地温的影响具有双重性: 在不同域值条件下, 它可增高或降低地温. 地温随植被覆盖度减小而逐渐增高, 但覆盖度减到0～20%时, 地温反而降低. 在青藏高原东部、南部和腹部的高山区, 冷季降雪多, 很多地段为稳定积雪区, 雪盖厚, 持续时间长, 对浅层地温起保温作用;而高原腹部的高平原、河谷和盆地冷季降雪较少, 雪盖薄, 持续时间较短, 一般保温作用微弱. 当雪盖厚度超过20 cm以后, 保温作用即开始增强;在暖季因积雪存在时间短, 雪盖薄, 短期内对浅层地温起冷却作用. 总之, 每种局地因素迫使地温向相反方向转化阶段是一个区间值, 为渐变过程. 随时空尺度变化, 局地因素的影响变化很大. 有些地段, 几种局地因素共同作用, 加上活动构造和地形、地貌等的影响, 使地温的时空分布和局地因素对其影响或控制变得错综复杂. 因此, 研究和预测地温特征和变化趋势, 需要在监测植被和积雪作用的基础上进行参数选择、 验证和优化.     

东北多年冻土区埋地输油管道周围温度场特征非线性分析

为解决冻土区输油管道周围土壤的温度计算问题,根据考虑相变瞬态温度场的控制微分方程,应用Galerkin法推导出了二维温度场的有限元计算公式.以东北多年冻土区中俄原油管道工程为背景,根据该工程区的冻土条件和气候条件,应用该方法对温热型输油管道土壤温度场进行了计算预报与对比分析.结果表明:对于输送油温为15 ℃、直径为0.914 m以及管顶埋深为2.0 m的管道,在没有铺设保温材料情况下,管顶之上的土壤在管道运行的第1年就达到热平衡状态,同时土壤融化速率在第1年达到最大,随后4a时间里迅速减小,第5年后融化速率变化趋于稳定;管道运行一段时间后,管道周围的融化圈随冷暖季节的变化呈交替式的扩展;在管道运行30 a后,融深＞10 m,即管底下的融化层厚＞7 m,而在铺设5～8 cm的聚氨酯保温材料后,融深控制在3.08～3.88 m,即管底下融化层厚为0.2～1.0 m.因此,合理使用保温方法能有效防止冻土区管道冻害的发生,同时达到保护冻土环境的目的.     

中国-俄罗斯原油管道工程(漠河-大庆段)冻土工程地质考察与研究进展

在2005-2007年期间,先后3次对中国-俄罗斯原油管道漠河-大庆段沿线的冻土工程地质条件等进行科学考察,开展了冻土工程地质条件及其在气候变化和人类活动作用下的评价和预测研究.考察研究结果表明:管道沿线多年冻土在各类融区、季节冻土和水系等分隔作用下呈片状或岛状分布,沿线岛状、稀疏岛状及零星岛状占多年冻土区段的40%左右;管道沿线多年冻土随着气候的转暖和人类活动的影响不断退化.地形地貌单元、植被分布、地表水分条件的变化等局部因素对多年冻土的分布和地下冰的赋存产生重要的影响,管道沿线大约分布有50 km左右的沼泽湿地,其表层为腐殖质土及泥炭层,泥炭层下面分布着含土冰层或地下冰,是管道沿线最差的冻土工程地质地段;由于中俄原油管道沿线水系发育多,冻胀丘、冰椎和冰幔等不良冻土现象广泛分布.科学考察的成果为管道沿线冻土工程地质条件评价和预测、管道的稳定性影响分析以及后期的长期检测系统设置等研究奠定坚实的基础,进一步为即将开工的中俄原油管道漠河-大庆段工程的设计、施工提供科学依据.