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The Proterozoic Bamble Sector, South Norway, is one of the world＇s classic amphiboliteto granulite- facies transition zones. It is characterized by a well-developed isograd sequence, with isolated ＇granulite-facies islands＇ in the amphibolite-facies portion of the transition zone. The area is notable for the discovery of C02-dominated fluid inclusions in the granolite-facies rocks by Jacques Touter in the late 1960＇s, which triggered discussion of the role of carbonic fluids during granulite genesis. The aim of this review is to provide an overview of the current state of knowledge of the Bamble Sector, with an emphasis on the Arendal-Froland-Nelaug-Tvedestrand area and off shore islands （most prominantly Tromay and Hisoy） where the transition zone is best developed. After a brief overview of the history of geological research and mining in the area, aspects of sedimentary, metamorphic and magmatic petrology of the Bamble Sector are discussed, including the role of fluids. Issues relevant to current geotectonic models for SW Scandinavia, directly related to the Bamble Sector, are discussed at the end of the review. 相似文献
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通过钾盐矿床与晶间卤水分异特征及成因的分析对比，认为晶间卤水分异的过程也就是钾盐矿床形成的过程。胶结浸染状固体矿形成于晶间卤水分异初期的浓缩阶段，改造于分异后期的淡化阶段；晶间卤水矿和层状固体矿形成于淡化阶段。 相似文献
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本湖Ｓ３盐层晶间卤水（简称晶卤）分异的成因是一个与钾盐矿床的成因及最佳开发密切相关的基本理论问题。文献［１－２］提出了晶卤分异成因新观点（阶段性淡化说）的基本理论框架。继文献［３］之后，本文对晶卤分异的又一复杂地区进行了深入解剖，为阶段性淡化说再次提供大量事实依据，具有一定的理论和经济意义。 相似文献
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塔里木盆地下奥陶统蓬莱坝组白云岩成因及储层主控因素分析——以巴楚大班塔格剖面为例 总被引：1，自引：1，他引：0
寒武系-下奥陶统白云岩是塔里木盆地非常重要的勘探接替领域,但由于白云岩埋藏深度大,勘探和研究程度低,目前的认识程度无法满足勘探的需求,尤其是白云岩储层成因和分布的认识。本文以巴楚地区大班塔格剖面蓬莱组白云岩的精细解剖为例,测制解剖剖面9条,采集样品195块,系统的开展了岩石薄片、物性及地球化学特征分析,取得了两个方面的新的认识。1)是塔里木盆地蓬莱坝组发育粉晶、细晶、中晶和粗晶四种白云岩,主要形成于早-中埋藏期与海源流体有关的白云石化作用中,局部受到热液改造,其晶粒大小与原岩结构的粗细及孔隙空间的大小有关,原岩结构粗,形成的白云石晶粒就粗,原岩孔隙空间大,白云石晶粒就大。2)是白云岩储层的分布具成层性和旋回性,孔隙发育段总体位于向上变浅旋回的顶部,与高频旋回的暴露面有关,其载体以细-粗晶白云岩为主,孔隙主体来自原岩孔隙的继承和再调整,少量来自埋藏(热液)溶蚀作用,而并不是传统观点所认为的白云石化作用建造孔隙,这一认识对塔里木盆地深层白云岩有效储层预测具重要的指导意义。 相似文献
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Mechanical properties of high porosity chalks are strongly dependent on the type of fluid in the pores. Dry chalk is considerably stronger than water-saturated chalk, and this phenomenon is often referred to as the water-weakening effect. To address the problem of chalk–fluid interactions, several series of tests have been performed with glycol and high concentration brines as saturating fluids. Glycol is a fluid that in many aspects resembles oil, except that glycol is miscible with water. Glycol-saturated chalk turns out to have properties very similar to oil-saturated chalk. Compared to dry chalk, both oil and glycol make the chalk somewhat weaker, but this weakening effect is much less than with water. Several series of tests with brines with high concentrations of calcium chloride or sodium chloride show that the water-weakening effect is considerably reduced in high ionic strength solutions. Most tests were performed as quasi-hydrostatic tests, with a constant stress ratio of 0.9. In such tests, the yield point marks the onset of accelerated pore collapse, and the yield value is close to the hydrostatic yield stress. In addition to these compressive tests, a series of Brazilian tests were performed, revealing the same trend. The variations in mechanical strength have been correlated with the activity of water in the brines. Within the experimental accuracy of the compressive tests, there is a linear trend between reduction of water activity and the corresponding increase in strength. This leads to the hypothesis that the water activity may be a key parameter in the water-weakening mechanism. But this conclusion also indicates that water weakening may be a special case of general chalk–fluid interactions where the degree of weakening depends on the strength of adsorption of the fluid molecules to the calcite surfaces. 相似文献
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Karsten Michael Hans G. Machel Stefan Bachu 《Journal of Geochemical Exploration》2003,80(2-3):193-219
Analysis of hydraulic heads and chemical compositions of Devonian formation waters in the west central part of the Alberta Basin, Canada, characterizes the origin of formation waters and migration of brines. The Devonian succession in the study area lies 2000–5000 m below the ground surface, and has an approximate total thickness of 1000 m and an average slope of 15 m/km. Four Devonian aquifers are present in the study area, which form two aquifer systems [i.e., a Middle–Upper Devonian aquifer system (MUDAS) consisting of the Elk Point and Woodbend–Beaverhill Lake aquifers, and an Upper Devonian aquifer system (UDAS) consisting of the Winterburn and Wabamun aquifers]. The Ireton is an effective aquitard between these two systems in the eastern parts of the study area. The entire Devonian succession is confined below by efficient aquitards of the underlying Cambrian shales and/or the Precambrian basement, and above by overlying Carboniferous shales of the Exshaw and Lower Banff Formations.The formation water chemistry shows that the Devonian succession contains two distinct brine types: a ‘heavy brine,’ located updip, defined approximately by TDS >200 g/l, and a ‘light brine’ with TDS <200 g/l. Hydraulic head distributions suggest that, presently, the ‘light brine’ attempts to flow updip, thereby pushing the ‘heavy brine’ ahead. The interface between the two brines is lobate and forms large-scale tongues that are due to channeled flow along high-permeability pathways. Geological and hydrogeochemical data suggest that the following processes determined the present composition of the ‘light’ and ‘heavy’ brines: original seawater, evaporation beyond gypsum but below halite saturation, dolomitization, clay dehydration, gypsum dewatering, thermochemical sulfate reduction (TSR), and halite dissolution. The influx of meteoric (from the south) and metamorphic (from the west) waters can be recognized only in the ‘light brine.’ Albitization can be unequivocally identified only in the ‘heavy brine.’ The ‘heavy brine’ may be residual Middle Devonian evaporitic brine from the Williston Basin or the Elk Point Basin, or it may have originated from partial dissolution of thick, laterally extensive Middle Devonian evaporite deposits to the east of the study area. The ‘light brine’ most probably originated from dilution of ‘heavy brine’ in post-Laramide times. 相似文献
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The geochemistry of 5 salt springs in the southwestern Mamfe Basin was investigated in order to infer the mineral content of their source and to relate the genesis of the springs to the local geology. Field observations revealed that, they are cold springs (23–28 °C), and are composed of secondary brines that are neutral to alkaline with pH values ranging from 7 to 8.7. Results of chemical analysis show that the springs contain major ions that form evaporite minerals, as well as chalcophile elements. The dominant cation is Na+ (>96%), and the dominant anion is Cl− (>99%). Based on correlation coefficients between ions that form evaporites and field occurrence of efflorescences of halite, it is suggested that the ancient evaporites in the Mamfe Basin are composed entirely of carbonate and chloride salts. Meteoric and convective fluid flow processes are responsible for the dissolution of ancient evaporites and subsequent migration of brines to the surface from underground. The brines migrate through permeable strata with migration pathways resulting from a combination of fracture porosity created by post––Cretaceous tectonism and intergranular porosity enhanced by the chemically aggressive migrating brines. 相似文献
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Dynamic leaching tests are important studies that provide more insights into time-dependent leaching mechanisms of any given solid waste. Hydrogeochemical modeling using PHREEQC was applied for column modeling of two ash recipes and brines generated from South African coal utility plants, Sasol and Eskom. The modeling results were part of a larger ash–brine study aimed at acquiring knowledge on (i) quantification and characterization of the products formed when ash is in contact with water–brines in different scenarios, (ii) the mineralogical changes associated with water–brine–ash interactions over time, (iii) species concentration, and (iv) leaching and transport controlling factors. The column modeling was successfully identified and quantified as important reactive mineralogical phases controlling major, minor and trace elements’ release. The pH of the solution was found to be a very important controlling factor in leaching chemistry. The highest mineralogical transformation took place in the first 10 days of ash contact with either water or brines, and within 0.1 m from the column inflow. Many of the major and trace elements Ca, Mg, Na, K, Sr, S(VI), Fe, are leached easily into water systems and their concentration fronts were high at the beginning (within 0.1 m from the column inflow and within the first 10 days) upon contact with the liquid phase. However, their concentration decreased with time until a steady state was reached. Modeling results also revealed that geochemical reactions taking place during ash–water–brine interactions does affect the porosity of the ash, whereas the leaching processes lead to increased porosity. Besides supporting experimental data, modeling results gave predictive insights on leaching of elements which may directly impact on the environment, particularly ground water. These predictions will help develop scenarios and offer potential guide for future sustainable waste management practices as a way of addressing the co-disposal of brines within inland ash dams and heaps. 相似文献
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别勒滩位于察尔汗盐湖西部边缘地区,与东台吉乃尔盐湖接壤,同处柴达木盆地拗陷中心,在整个柴达木盆地盐湖中也是Li元素相对富集的地段之一。该地段在距北岸10 km的范围内,Li平均含量为0.594 g/L,最高可达1.225 g/L,与东台吉乃尔盐湖晶间卤水中Li含量很接近,但Mg/Li比值高出东台吉乃尔盐湖23倍。该地段Li的水平分布大致可划分为3个区域:Ⅰ区Li含量为1.03倍。该地段Li的水平分布大致可划分为3个区域:Ⅰ区Li含量为1.01.2 g/L;Ⅱ区Li含量为0.41.2 g/L;Ⅱ区Li含量为0.40.6 g/L;Ⅲ区Li含量为0.20.6 g/L;Ⅲ区Li含量为0.20.3 g/L,其变化趋势是由北向南逐渐降低。别勒滩干盐湖底部盐层形成于距今25 000 a,上部盐层成盐期大约距今15 000 a。别勒滩西部边缘的涩聂湖是在大约距今10 000 a左右形成的新的具有表面卤水的全新世盐湖,该湖也是别勒滩区段主要物质来源的汇集区和补给区。 相似文献