广西大厂超大型锡矿的形成条件与成矿模式

超大型矿床的形成条件有其特殊性.大厂超大型锡矿产出于南丹-昆仑关基底性深大断裂带上,经过多旋回构造-岩浆活动使矿质继承叠加,最后聚积于燕山晚期的岩浆热液中.大厂超大型锡矿床是各种成矿因素良好匹配,并经长时期的多重富集综合作用的结果.     

下庄矿田湖子地区铀矿找矿方向探讨

湖子地区位于NNE向诸广-新兴铀成矿带与近EW向大东山-漳州大断裂复合部位,是华南早、晚两期铀成矿热液活动叠加区、放射性高场区,既有"硅化带大脉"型铀矿产出,又有"交点"型铀矿存在,找矿前景良好.文章在论述下庄矿田铀成矿地质环境、铀成矿特征及铀矿定位条件基础上,分析了湖子地区铀成矿条件与找矿前景,指出该区今后铀矿找矿方向是:① 6009号硅化断裂带,在其北段找硅化带大脉型铀矿,在其南段找"交点"型铀矿;②新桥-下庄硅化断裂带和6009号带之间成矿部位,寻找硅化带型和"交点"型铀矿;③NW向、近EW向辉绿岩脉与NNE向、NE向构造交汇部位(交点),寻找"交点"型铀矿.     

粤东成矿地质背景及银-铜-铅-锌成矿物质来源探讨

通过对粤东地区地层和岩石中成矿元素含量和区域地质背景的分析,认为粤东地区铜铅-锌-银成矿作用与燕山期的构造-岩浆作用关系密切,成矿物质中银-铜-锌以下地壳来源为主,铅则以上地壳及沉积地层来源为主。     

利国矿区铜（金）成矿条件的研究

利国矿区是江苏省重要铁矿基地之一,矿区位于秦岭一昆仑纬向构造带东延的南侧与新华夏构造体系第三隆起带的交接复合部位。铁矿床主要产于燕山期闪长玢岩杂岩体与下奥陶统碳酸盐地层的接触带及其附近灰岩中,矿体呈似层状一透镜状等,产状与围岩一致,具层控矿床的特征。笔者主要从成矿地质特征着手,分析总结了该区铜、金矿化特征及主要成矿规律,指出了利国矿区铜（金）矿的找矿方向和有望靶区。     

岩石中的渗透率、流体流动及热液成矿作用

热液成因的固体金属矿床形成过程中都曾拥有一段流动的历史。成矿物质以溶液的形式从矿源地穿过孔隙或断裂达到了现在的栖身之所,在此过程中流体通过的路径决定了它们的走向,而溶液本身也改变了路径的特征。因此,对于此类矿床的研究不能仅仅囿于眼之所见,而应将古流体流动的观念融入其中,并考察它们的跋涉之路。文中总结了近年来国内外在岩石孔隙、断裂介质及与其相关渗透率对热液成矿作用的控制等领域的研究成果和最新进展,对岩石渗透率、渗透率的影响因素、岩石中流体流动的特征等问题进行了阐述,讨论了渗透率对于热液成矿作用深度、成矿规模、矿质沉淀机制等方面的重要影响,藉此在固体金属矿床研究中强化流"体运动"的观念,并促进构造地质学和成矿作用地球化学间一个新研究方向的发展。     

幔源CO_2释出机理、脱气模式及成藏机制研究进展

针对幔源CO2如何从地幔岩浆中脱出并进入沉积地层中形成CO2气藏聚集这一关键问题,总结了国内外研究进展和前缘方向。研究表明,地幔深部的碱性玄武岩浆和碱性岩浆才是深部流体和CO2等挥发份大量赋存、渗滤和释出的场所。浅成侵入岩、次火山岩和火山通道等是CO2释放和聚集的有利位置,岩浆期后和岩浆衰弱期的热液活动阶段是CO2大量释放和聚集的有利时期。幔源CO2进入沉积盆地中具有3种脱气模式,即沿岩石圈断裂直接脱气模式、热流底辟体脱气模式和壳内岩浆房-基底断裂组合脱气模式。CO2的固有物化性质决定其运移相态多样,具有运移和聚集过程同步的特征。只有在满足大量的化学消耗及地层水或原油的溶解和耗散之后才能形成CO2有效聚集。幔源CO2成藏和分布主要受岩浆气源体和气源断裂体系的控制。今后,在超临界CO2及其对油气运移聚集的作用、CO2与深大断裂及火山岩的关系、CO2脱气运移机制、CO与常规烃类油气的耦合差异成藏机制等方面仍需要进一步的研究和探索。     

热液成矿作用的地质地球化学动力学——以胶东牟平-乳山金矿带为例

通过对胶东牟平—乳山热液脉状金,铅锌矿床成矿动力学控制规律的研究,说明了建立热液成矿反应体系的方法,并得出以下认识:（1）区域断裂构造活动,通过影响成矿反应体系的热力学性质和条件,控制元素的富集和分散。（2）热液成矿过程中容矿断裂活动可划分为两种作用方式:脆性破裂和韧—脆性张开,构成热液成矿的两种构造动力学环境。（3）热液成矿反应体系是一种开放的动态的热力学体系。断裂的脆性破裂阶段,使体系处于强烈的过饱和状态,矿质在远离平衡状态下快速结晶,加剧物质分异;在脆—韧性张开阶段,矿质在接近平衡态体系中缓慢晶出。（4）热液演化晚期,金在残余溶液中富集;当断裂再次发生构造脉动震颤时,早期形成的块状黄铁矿矿石碎裂,富金溶液充填其中,形成含裂隙金和晶隙金的富矿石。成矿体系热力学演化与构造动力学条件有利的匹配控制着富矿石的形成。     

Fluid sources for the La Guitarra epithermal deposit (Temascaltepec district, Mexico): Volatile and helium isotope analyses in fluid inclusions

The La Guitarra deposit (Temascaltepec district, South-Central Mexico), belongs to the low/intermediate sulfidation epithermal type, has a polymetallic character although it is currently being mined for Ag and Au. The mineralization shows a polyphasic character and formed through several stages and sub-stages (named I, IIA, IIB, IIC, IID, and III). The previous structural, mineralogical, fluid inclusion and stable isotope studies were used to constrain the selection of samples for volatile and helium isotope analyses portrayed in this study. The N₂/Ar overall range obtained from analytical runs on fluid inclusion volatiles, by means of Quadrupole Mass Spectrometry (QMS), is 0 to 2526, and it ranges 0 to 2526 for stage I, 0 to 1264 for stage IIA, 0 to 1369 for stage IIB, 11 to 2401 for stage IIC, 19 to 324 for stage IID, and 0 to 2526 for stage III. These values, combined with the CO₂/CH₄ ratios, and N₂-He-Ar and N₂-CH₄-Ar relationships, suggest the occurrence of fluids from magmatic, crustal, and shallow meteoric sources in the forming epithermal vein deposit. The helium isotope analyses, obtained by means of Noble Gas Mass Spectrometry, display R/Ra average values between 0.5 and 2, pointing to the occurrence of mantle-derived helium that was relatively diluted or “contaminated” by crustal helium. These volatile analyses, when correlated with the stable isotope data from previous works and He isotope data, show the same distribution of data concerning sources for mineralizing fluids, especially those corresponding to magmatic and crustal sources. Thus, the overall geochemical data from mineralizing fluids are revealed as intrinsically consistent when compared to each other.The three main sources for mineralizing fluids (magmatic, and both deep and shallow meteoric fluids) are accountable at any scale, from stages of mineralization down to specific mineral associations. The volatile and helium isotope data obtained in this paper suggest that the precious metal-bearing mineral associations formed after hydrothermal pulses of predominantly oxidized magmatic fluids, and thus it is likely that precious metals were carried by fluids with such origin. Minerals from base-metal sulfide associations record both crustal and magmatic sources for mineralizing fluids, thus suggesting that base metals could be derived from deep leaching of crustal rocks. At the La Guitarra epithermal deposit there is no evidence for an evolution of mineralizing fluids towards any dominant source. Rather than that, volatile analyses in fluid inclusions suggest that this deposit formed as a pulsing hydrothermal system where each pulse or set of pulses accounts for different compositions of mineralizing fluids.The positive correlation between the relative content of magmatic fluids (high N₂/Ar ratios) and H₂S suggests that the necessary sulfur to carry mostly gold as bisulfide complexes came essentially from magmatic sources. Chlorine necessary to carry silver and base metals was found to be abundant in inclusion fluids and although there is no evidence about its source, it is plausible that it may come from magmatic sources as well.     

Albite vein formation during exhumation of high-pressure terranes: a case study from alpine Corsica

The formation of late‐stage veins can yield valuable information about the movement and composition of fluids during uplift and exhumation of high‐pressure terranes. Albite veins are especially suited to this purpose because they are ubiquitously associated with the greenschist facies overprint in high‐pressure rocks. Albite veins in retrogressed metabasic rocks from high‐pressure ophiolitic units of Alpine Corsica (France) are nearly monomineralic, and have distinct alteration haloes composed of actinolite + epidote + chlorite + albite. Estimated P–T conditions of albite vein formation are 478 ± 31 °C and 0.37 ± 0.14 GPa. The P–T estimates and petrographic constraints indicate that the albite veins formed after the regional greenschist facies retrogression, in response to continued decompression and exhumation of the terrane. Stable isotope geochemistry of the albite veins, their associated alteration haloes and unaltered hostrocks indicates that the vein‐forming fluid was derived from the ophiolite units and probably from the metabasalts within each ophiolite slice. That the vein‐forming fluid was locally derived means that a viable source of fluid to form the veins was retained in the rocks during high‐pressure metamorphism, indicating that the rocks did not completely dehydrate. This conclusion is supported by the observation of abundant lawsonite at the highest metamorphic grades. Fluids were liberated during retrogression via decompression dehydration reactions such as those that break down hydrous high‐pressure minerals like lawsonite. Albite precipitation into veins is sensitive to the solubility and speciation of Al, which is more pressure sensitive than other factors which might influence albite vein formation such as silica saturation or Na:K fluid ratios. Hydraulic fracturing in response to fluid generation during decompression was probably the main mechanism of vein formation. The associated pressure decrease with fracturing and fluid decompression may also have been sufficient to change the solubility of Al and drive albite precipitation in fracture systems.     

Computer simulation studies of Crystallization under confinement conditions

Crystallization under confinement conditions is a very important process in geochemistry and geophysics. Computer simulations of fluids in nanometer scale pore spaces can provide a unique microscopic insight into the structure, dynamics and forces arising from the crystallization process. We discuss in this paper molecular dynamics computer simulations of crystallization in pores of nanometer dimensions. The crystallization pressure due to the freezing of a model of Argon in a nanopore is computed using molecular dynamics simulations. We also investigate the influence of pore geometry in determining the dynamics of confined fluids, as well as mass separation in binary mixtures. It turns out that the pore geometry reveals itself as an important variable, leading to 1) new mechanisms for fast diffusion in confined spaces, and 2) accumulation of solute in specific regions inside the pore.