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1.
铁元素是岩浆-热液成矿系统中参与成矿的重要金属元素之一,岩浆-热液矿床中富铁矿物(黄铁矿、磁铁矿、黄铜矿、磁黄铁矿、斑铜矿、毒砂、菱铁矿)的δ56Fe值变化较大(-2.07‰～+1.58‰),指示铁同位素在岩浆演化、流体出溶和热液演化过程中均存在明显的分馏,因此,在约束岩浆-热液成矿系统中成矿金属的迁移-富集-沉淀过程和示踪成矿物质来源方面具有巨大的应用潜力。通过整理和分析前人研究资料,文章总结了岩浆-热液成矿系统岩浆演化、流体出溶和热液演化过程中铁同位素地球化学行为的研究现状。岩浆演化过程中铁同位素会发生显著分馏,如部分熔融过程中,熔体相比残余固相富集重铁同位素;矿物分离结晶会引起残余熔体铁同位素组成的变化,主要受含Fe2+或Fe3+矿物结晶的影响,如磁铁矿分离结晶会导致残余熔体铁同位素组成变轻,总体反映岩浆氧化还原状态对铁同位素分馏的主要控制作用,因此,含矿岩体铁同位素组成及其变化可用于确定岩浆的氧化还原状态。流体出溶是含矿岩浆演化成为岩浆热液矿床的关键过程,出溶流体相对于母岩富集轻铁同位素,但实验研究表明出溶流体铁... 相似文献
2.
地质流体是一定地质作用的产物，而矿床的形成过程与特定地质构造背景下地质流体的产生、运移和聚集有着密切联系。不同成矿流体的成矿机制各有差异。岩浆热液因温度降低、压力减小等因素使热液中成矿物质达到过饱和，从而产生矿质沉淀；沉积盆地含矿热卤水流体在热对流、沉积压实等作用下运移、充填、聚集；与海底基性火山活动有关的现代大洋海底热液形成硫化物矿床；地幔流体的碱交代作用形成大型一超大型中高温热液矿床。在具体的成矿过程中，各种构造环境又对流体中的成矿元素的分配、集中起到至关重要的控制作用。 相似文献
3.
传统地质学理论认为花岗岩是由异地深熔的花岗岩浆沿构造侵入至地壳浅部冷凝结晶形成的,"原地重熔-壳内对流"理论认为熔融的花岗岩浆并没有离开源区,而是原地重熔,熔融岩浆层内的热能对流形成大规模层状或似层状花岗岩浆,岩浆层冷凝结晶形成花岗岩,花岗岩体是岩浆层界面(MI)凸起形成的。燕山晚期花岗闪长斑岩是紫金山矿集区成矿母岩,在温度差和压力差作用下,成矿元素和挥发分在MI凸起界面上部富集形成含矿流体,在沿构造裂隙向上向外逃逸过程中与围岩产生水岩反应,形成从高温到低温热液蚀变分带,而不同成矿元素则在不同温度、压力(深度)和Eh、pH区间沉淀成矿,形成罗卜岭斑岩型铜钼矿、紫金山高硫化中低温热液型铜金矿和悦洋低硫化低温热液型银多金属矿,它们是同一斑岩-浅成热液成矿体系的产物。 相似文献
4.
云南墨江金矿床的同位素地球化学及成因探讨 总被引：4，自引：1，他引：3
墨江金矿的同位素地球化学特征,成矿元素组合和包裹体成分表明：成矿物质主要来源于金厂蚀变超基性岩体,成矿热液是深源流体,岩浆水和大气降水混合的产物。成矿期深部富矿化剂流体沿断裂上升并与地下水混合,从侵入体及围岩中淋滤出了成矿物质。在迁移过程中,随着地球化学条件的改变,金在有利部位沉淀富集形成矿床。墨江金矿床属混合热液改造型矿床。 相似文献
5.
桂东南金银矿床成矿规律与成矿模式 总被引：3，自引：0，他引：3
根据桂东南金银矿床成矿地质条件，典型金银矿床的硫、氢、氧、铅同位素、稀土元素、矿物包裹体流体组份和成矿物理化学条件，提出了桂东南金银矿床的混合岩化－岩浆热液型和变质－岩浆热液型的成因类型，并建立了桂东南金银矿床的成矿模式。即地槽发展时期形成矿源层；变质－混合岩化作用促进金银组份活化迁移与初始富集；剥离作用使金银组份再次迁移富集；燕山期构造－岩浆作用成矿。 相似文献
6.
根据金矿床中碲、硒赋存特点与富集程度,可将Au-(Ag)-Te-Se成矿系统的矿床成因类型划分为:(1) 浅成低温热液型金-银矿床;(2) 造山型金矿床;(3) 卡林-类卡林型金矿床;(4) 碱性-偏碱性侵入岩型金矿床;(5)斑岩型(铜)金矿床;(6) 夕卡岩型(铜)金矿床;(7) VMS型金多金属矿床。碲、硒都是亲地幔的元素,侵入岩与火山岩是Au-(Ag)-Te-Se成矿系统中碲、硒的重要来源,黑色岩系也是硒的重要来源。温度、pH、氧逸度等是控制Te、Se的迁移与富集的重要因素。Au-(Ag)-Te-Se成矿系统的成矿机制与岩浆脱气、流体-熔体分离、水-岩反应、流体沸腾与混合、有机作用密切相关。其中岩浆脱气、流体-熔体分离、流体沸腾与流体混合是碲化物型金矿床的重要成矿机制,而水-岩反应、流体混合、有机作用是硒化物型金矿床的重要成矿机制。在成矿过程中,先期形成一些亚稳定或不稳定的过渡态矿物易发生固溶体分离作用,或是不饱和流体与已形成的矿物发生溶解-再沉淀作用,导致矿石具有丰富的物质组成和结构特点。 相似文献
7.
为了解锡田钨锡多金属矿床的成矿流体演化过程和成矿元素迁移机制,深入揭示成矿机制,指导该地区的下一步找矿勘探工作,对黑钨矿、锡石及透明矿物的流体包裹体进行了岩相学观察、红外显微测温及LA-ICP-MS原位分析.显示锡田钨锡多金属矿床绿柱石、黑钨矿中发育流体-熔体包裹体,均一温度最高可达760℃.早成矿阶段流体均一温度为360~500℃,盐度主要为28.4%~41.5% NaCleqv,主成矿阶段均一温度为280~450℃,盐度主要为3.0%~20.0% NaCleqv.,晚成矿阶段均一温度为120~280℃,盐度为0.4%~6.6% NaCleqv..LA-ICP-MS分析表明,超临界流体开始出溶时,W、Cu、Mo等元素优先富集于富挥发分气相中,Pb、Zn、Sn、Fe、Mn等元素则更倾向富集于高盐度卤水相中.锡田钨锡多金属矿床成矿流体来源于燕山期浅源花岗岩,钨锡成矿作用始于岩浆-热液过渡阶段,成矿流体具有高温、高盐度和富CO2等特征.成矿流体来自岩浆流体的出溶,演化过程中经历了两次不混溶作用,不混溶相分离过程中,成矿元素选择性迁移,在各相中进行不均匀分配.流体不混溶、水岩反应、流体混合和流体冷却作用是导致该矿床钨锡矿物沉淀的原因. 相似文献
8.
安徽铜陵凤凰山铜矿床地球化学特征及其意义 总被引：12，自引：4，他引：8
通过对凤凰山铜矿床化探样品测试数据的系统分析研究,初步确定了本矿床在成矿作用过程中至少经历了两次大的热液流体活动:第一次是花岗闪长岩的侵入,不仅是岩浆热液使成矿元素迁移富集,而且在岩体侵入过程中强大热能的驱动下地层中的大气水参与流体的对流循环,使地层中的成矿元素被迁移;第二次是石英二长闪长岩的侵入,它在带来大量成矿物质的同时,也使地层中、特别是前期花岗闪长岩中的成矿元素在大气水的对流循环作用下被迁移并在岩体边缘及附近富集成矿. 相似文献
9.
世界上所有的铂族金属矿床都有热液流体活动的迹象。影响铂族元素(PGE)成矿的流体主要有两类:堆晶体后期流体(>500℃)和岩浆后期流体(<500℃)。低温热液(<500℃)中,PGE可能主要以氯络合物及氢硫基络合物的形式运移;高温热液(>500℃)中,PGE可能主要以氯络合物的形式运移。在详细论述不同温度、压力条件下的热液流体中PGE溶解性质的基础上,分析了PGE在流体中的溶解、迁移、富集及可能的沉淀机制,为探寻PGE矿床的成因提供一个突破口。 相似文献
10.
本文主要介绍了当前热液成矿物理化学条件研究方面的某些进展。其中包括:从岩浆的聚合作用引伸到热液的聚合作用,并用实验证明热液中许多元素呈聚合物形式存在;重视羟基络合物在热液中的作用;从建立单一元素的迁移模式转向建立成矿元素和造岩元素的化合迁移模式;流体压力的改变可能是促使成矿元素沉淀的重要因素;从定性分析发展到建立含矿热液迁移的定量模式。 相似文献
11.
12.
Alexandro Scislewski 《Geochimica et cosmochimica acta》2010,74(24):6996-7007
Mineral dissolution and precipitation reactions actively participate to control fluid chemistry during water-rock interaction. However, it is difficult to estimate and normalize bulk reaction rates if the mineral surface area effectively participating in the reactions is unknown. In this study, we evaluated the changing of the reactive mineral surface area during the interaction between CO2-rich fluids and albitite rock reacting under flow-through conditions. Our methodology, adopting an inverse modelling approach, is based on the measured chemical fluid composition as raw data. We estimated the rates of dissolution and the reactive surface areas of the different minerals by reconstructing the chemical evolution of the interacting fluids. This was done by a reaction process schema that was defined by a fractional degree of advance of the irreversible mass-transfer process and by attaining the continuum limit during the water-rock interaction. Calculations were carried out for albite, microcline, biotite and calcite assuming that the ion activity of dissolved silica and aluminium ions was limited by the equilibrium with quartz and kaolinite.We found that the absolute dissolution rate of albite, microcline, biotite and calcite remains essentially constant as a function of time, and the calcite dissolution rate is orders of magnitude higher than silicate minerals. On the contrary, the reactive surface area of the parent minerals varied by more than two orders of magnitude during the observed reaction time, especially for albite. We propose that the reactive surface area depends mainly on the stability of the secondary mineral coating that may passivate the effective reactive surface area of the parent minerals. 相似文献
13.
Hydrothermal mixing,carbonate dissolution and sulfide precipitation in Mississippi Valley-type deposits 总被引：1，自引：0，他引：1
A large number of Mississippi Valley-Type (MVT) deposits are located within dissolution zones in carbonate host rocks. Some genetic models propose the existence of cavities generated by an earlier event such as a shallow karstification, that were subsequently filled with hydrothermal minerals. Alternative models propose carbonate dissolution caused by the simultaneous precipitation of sulfides. These models fail to explain either the deep geological setting of the cavities, or the observational features which suggest that the dissolution of carbonates and the precipitation of minerals filling the cavities are not strictly coeval. We present a genetic model inspired by the textural characteristics of MVT deposits that accounts for both the dissolution of carbonate and precipitation of sulfides and later carbonates in variable volumes. The model is based on the mixing of two hydrothermal fluids with a different chemistry. Depending on the proportion of the end members, the mixture dissolves and precipitates carbonates even though the two mixing solutions are both independently saturated in carbonates. We perform reactive transport simulations of mixing of a regional groundwater and brine ascending through a fracture, both saturated in calcite, but with different overall chemistries (Ca and carbonate concentrations, pH, etc). As a result of the intrinsic effects of chemical mixing, a carbonate dissolution zone, which is enhanced by acid brines, appears above the fracture, and another zone of calcite precipitation builds up between the cavity and the surrounding rock. Sulfide forms near the fracture and occupies a volume smaller than the cavity. A decline of the fluid flux in the fracture would cause the precipitation of calcite within the previously formed cavities. Therefore, dissolution of carbonate host rock, sulfide precipitation within the forming cavity, and later filling by carbonates may be part of the same overall process of mixing of fluids in the carbonate host rock.Editorial handling: C. Everett 相似文献
14.
为了探索高渗透性洋壳中高温热液循环系统的形成机制,以数值模拟为手段研究热液循环中的矿物沉淀过程及其对洋壳渗透率的反馈.在热液对流-矿物反应模型中考虑了硬石膏、黄铁矿和黄铜矿的沉淀和溶解反应,基于矿物的溶度积计算矿物的沉淀/溶解量,并将其转换为渗透率的变化.结果显示,黄铁矿和黄铜矿分布于350~380℃等温线范围内,并随着热液温度升高而逐渐向海底推移.海水被加热及与热液混合过程中沉淀出硬石膏,在热液上升通道两侧形成低渗透性的烟囱状结构,降低了海水-热液混合程度从而使热液温度升高.高温热液通道建立后,便会有更多的金属物质随着高温热液被运输至浅层洋壳或海底.模拟结果为理解海底高温热液喷口的形成机制提供了借鉴. 相似文献
15.
Shallowly plunging and branching pipe systems in Lease and Bobbejaankop Granite at the Zaaiplaats mine are host to major tin mineralization. Detailed textural study of Maggs Pipe indicates that dissolution of the granite was a major process in the formation of open space which provided permeability for the passage of hydrothermal fluids, and sites for the precipitation of ore and gangue minerals. The pipe formation process initiates with the dissolution of granite quartz and subsequently extends to feldspar dissolution, particularly in the central portion of Maggs Pipe. Spaces created by mineral dissolution are filled by hydrothermal phases and the relict feldspar matrix becomes progressively more altered toward the centre of the pipe. The distribution of alteration and infill minerals defines a zoning pattern which, from the outer margin to the central core, includes calcite-quartz, chlorite (± cassiterite, albite, fluorite) and synchisite-calcite zones. It is postulated that quartz and feldspar dissolution resulted from interaction between the granite and hydrothermal fluids containing alkali-chloride, -fluoride or -carbonate complexes which had separated from the granite magma during crystallization. Preliminary observations on several other pipes at Zaaiplaats indicate that quartz and feldspar dissolution was a major procress in forming the pipe systems. 相似文献
16.
Kenichi HOSHINO Yuki YAMAMOTO Xiangping GU Su Young LEE Makoto WATANABE 《Resource Geology》2000,50(3):185-190
Abstract: Possible ore deposition by fluid mixing was preliminarily examined using MIX 99, a FORTRAN program developed for simulating water-rock interactions. We consider mixing of two fluids, the low fO2 and high temperature source fluid and the high fO2 and low temperature seawater. Oxygen fugacity of a mixed fluid formed by titration of seawater into the source fluid gradually decreases with decreasing temperature (model A). Sequential precipitation of ore-forming minerals was examined in this model. On the other hand, simultaneous precipitation of the minerals could be followed by simulation of instantaneous overall mixing of the two fluids (model B). Results of simulation of the both models revealed that a temporal sequence of mineralization observed in the Karuizawa mine, NE Japan, can be formed by model A, while model B is suitable for the mineralization of an active chimney found in the Rainbow hydrothermal area of the Mid-Atlantic Ridge. 相似文献
17.
Major minerals (sulfates, sulfides, quartz) are distributed in different parts of submarine hydrothermal ore deposits. For instance, the abundance of barite increases stratigraphically upwards in the massive orebodies of the Kuroko deposits (black and yellow ores), while quartz is abundant in the lower parts (siliceous ore). The different distribution of barite and quartz in the Kuroko deposits can not be accounted for by thermochemical equilibrium calculations based on the precipitation due to mixing of ascending hydrothermal solutions with ambient cold seawater. In the present study, a coupled fluid flow‐precipitation kinetics model was used to calculate the amounts of quartz, barite, and anhydrite precipitated from a hydrothermal solution mixed with seawater, assuming reasonable values for temperature, precipitation rate, fluid flow velocity, mineral surface area/fluid mass ratio (A/M), and initial concentrations of hydrothermal solution and seawater before mixing occurred. The results indicate that barite precipitates more efficiently than quartz from discharging fluids with relatively higher flow velocity, lower temperatures and under the condition of lower A/M ratios on the seafloor (black ore), whereas quartz precipitates more effectively from solutions with lower flow velocity, higher temperatures and higher A/M ratios beneath the seafloor (siliceous ore) and in the orebody (barite ore, ferruginous chert ore). Anhydrite precipitates in shallow sub‐seafloor environments with lower precipitation rates and higher A/M ratios than barite and higher precipitation rates and lower A/M ratios than quartz. These results explain the observed occurrences of barite, anhydrite, and quartz in the Kuroko deposits. Namely, barite is abundant in black ore and barite ore which formed above the seafloor, anhydrite formed in high‐permeability tuff breccias, and quartz formed in low permeability dacite intrusive bodies in the sub‐seafloor environment. 相似文献
18.
Chongbin Zhao Lynn B. Reid Klaus Regenauer-Lieb Thomas Poulet 《Computational Geosciences》2012,16(3):735-755
In dealing with chemical-dissolution-front propagation problems in fluid-saturated porous media, the chemical dissolution front represented by the porosity of the medium may have a very steep slope (i.e., a very large porosity gradient) at the dissolution front, depending on the mineral dissolution ratio that is defined as the equilibrium concentration of the dissolved minerals in the pore-fluid to the solid molar density of the dissolvable minerals in the solid matrix. When the mineral dissolution ratio approaches zero, the theoretical value of the porosity gradient tends to infinity at the chemical dissolution front. Even for a very small value of the mineral dissolution ratio, which is very common in geochemical systems, the porosity gradient can be large enough to cause the solution hard to converge when the conventional finite element method is used to solve a chemical dissolution problem in a fluid-saturated porous medium where the pore-fluid is compressible. To improve the convergent speed of solution, a porosity-gradient replacement approach, in which the term involving porosity-gradient computation is replaced by a new term consisting of pore-fluid density-gradient and pressure-gradient computation, is first proposed and then incorporated into the finite element method in this study. Through comparing the numerical results obtained from the proposed approach with the theoretical solutions for a benchmark problem, it has been demonstrated that not only can the solution divergence be avoid, but also the accurate simulation results can be obtained when the proposed porosity-gradient replacement approach is used to solve chemical-dissolution-front propagation problems in fluid-saturated porous media including pore-fluid compressibility. 相似文献
19.
This paper explores how dissolution and precipitation reactions are coupled in batch reactor experimental systems at elevated temperatures. This is the fourth paper in our series of “Coupled Alkali Feldspar Dissolution and Secondary Mineral Precipitation in Batch Systems”. In our third paper, we demonstrated via speciation-solubility modeling that partial equilibrium between secondary minerals and aqueous solutions was not attained in feldspar hydrolysis batch reactors at 90-300 °C and that a strong coupling between dissolution and precipitation reactions follows as a consequence of the slower precipitation of secondary minerals (Zhu and Lu, 2009). Here, we develop this concept further by using numerical reaction path models to elucidate how the dissolution and precipitation reactions are coupled. Modeling results show that a quasi-steady state was reached. At the quasi-steady state, dissolution reactions proceeded at rates that are orders of magnitude slower than the rates measured at far from equilibrium. The quasi-steady state is determined by the relative rate constants, and strongly influenced by the function of Gibbs free energy of reaction (ΔGr) in the rate laws.To explore the potential effects of fluid flow rates on the coupling of reactions, we extrapolate a batch system (Ganor et al., 2007) to open systems and simulated one-dimensional reactive mass transport for oligoclase dissolution and kaolinite precipitation in homogeneous porous media. Different steady states were achieved at different locations along the one-dimensional domain. The time-space distribution and saturation indices (SI) at the steady states were a function of flow rates for a given kinetic model. Regardless of the differences in SI, the ratio between oligoclase dissolution rates and kaolinite precipitation rates remained 1.626, as in the batch system case (Ganor et al., 2007). Therefore, our simulation results demonstrated coupling among dissolution, precipitation, and flow rates.Results reported in this communication lend support to our hypothesis that slow secondary mineral precipitation explains part of the well-known apparent discrepancy between lab measured and field estimated feldspar dissolution rates (Zhu et al., 2004). Here we show how the slow secondary mineral precipitation provides a regulator to explain why the systems are held close to equilibrium and show how the most often-quoted “near equilibrium” explanation for an apparent field-lab discrepancy can work quantitatively. The substantiated hypothesis now offers the promise of reconciling part of the apparent field-lab discrepancy. 相似文献
20.
Homogenization temperatures and salinity data are presented for fluid inclusions from hydrothermal gangue minerals (quartz and fluorite) associated with porphyry wolframite-molybdenite-arsenopyrite-sphaleritebismuth-chalcopyrite-cassiterite mineralization within the Fire Tower ore zone, Mt Pleasant, New Brunswick. The data indicate that ore mineral precipitation occurred within a temperature range of 260° to 490°C from moderate to high salinity (10–42 wt% NaCl equivalent) aqueous fluids. Two stages of hydrothermal activity characterized by high (>30 wt% NaCl equivalent) salinity fluids are recognized; one which occurred at relatively high temperature (350°–490°C); and one which took place at lower temperature (180°–250°C). The high salinity, high temperature stage is interpreted to be the result of resurgent boiling. Dilution of these early fluids by convecting meteoric water resulted in low to moderate salinity fluids, which dominate the inclusion population. The low temperature, high salinity fluid inclusions are interpreted to represent late residual fluids derived from boiling which occurred as a result of a change in the pressure regime from dominantly lithostatic to hydrostatic conditions. 相似文献