变质流体作用的元素地球化学研究

变质流体作用是变质岩－流体体系的重要地质作用过程，可以通过有效的地质地球化学方法揭示，综述了变质流体作用的地球化学研究进展，主要包括：流体包裹体，同位素和元素地球化学等方面，强调了元素地球化学研究对于示踪变质流体作用过程的重要性。     

变质流体研究新进展

变质流体是变质过程的主要动力学因素之一。目前变质流体研究主要集中在下部地壳麻粒岩相变质流体，俯冲带高压－超高压变质流体和接触变质流体等方面。研究的主要问题是流体流动机制和元素迁移，流体－岩石相互作用和流体来源。下部地壳麻粒岩相变质流体以ＣＯ２为主，具有较低的ａＨ２Ｏ。δ１３Ｃ研究表明大约２／３ＣＯ２是深成的。富ＣＯ２流体流动是紫苏花岗岩形成和热扰动的原因之一，也是麻粒岩形成和大离子亲石元素亏损的主要因素。俯冲带是高压、超高压变质作用发生和流体活动最活跃的场所。流体富含Ｈ２Ｏ、ＣＨ４和ＣＯ２，可以诱导部分熔融反应和岛弧岩浆作用。高压变质条件下的矿物稳定性也与流体有关。同位素研究表明，在超高压变质期间没有化学上完全相同的流体大规模循环。流体－熔体系统模式能更有效地解释下插板片的元素再循环。接触变质流体研究主要集中在含有易于发生流体－岩石反应的不纯碳酸盐岩地区。硅灰石带中流体／岩石比率高达４０∶１，表明接触变质岩石中有大量流体存在。接触变质过程流体成分有较大差异，主要取决于流体来源、原岩性质和侵入体特征。流体流动和循环模式受控于构造变形，岩浆作用和变质过程的动力学条件及流体成分。     

区域变质作用中的流体

区域变质条件下流体的流动有 4种标志 :( 1)细脉 ;( 2 )岩石学 ;( 3 )稳定同位素 ;( 4 )常量元素的交代作用。不同级别的区域变质作用中 ,流体影响着岩石的变质反应和变形 ;在高级变质的情况下甚至有熔体出现。在超高压变质条件下 ,流体量比地壳范围区域变质要少得多 ,从大别山超高压变质带的资料可知 ,流体的演化有明显的阶段性 ,局部曾发现熔融包裹体。水流体的介入 ,引起岩石的退变质和元素地球化学变异 ,是超高压变质岩抬升、进入中下地壳的产物。新近的实验岩石学成果说明 ,多硅白云母、角闪石等含羟基的矿物 ,在俯冲达 10 0km以下依然稳定 ,而一些花岗岩体系在超高压的条件下产生的超临界流体 ,乃是花岗岩、片麻岩只能部分保留超高压矿物组合的原因。     

近70年中国变质岩石学-变质地质学的研究进展

为总结我国变质地质学的历史经验,回顾了我国从变质岩石学到变质地质学近70年的发展历程.依据大量文献,分3个阶段和8个方面总结了变质岩石学和变质地质学取得的进展.我国在超高压变质地质学、早前寒武纪变质地质学、变质作用年代学、变质作用相平衡模拟等领域处于国际先进行列,蓝片岩、变质流体和变质岩化学动力学方面与世界研究基本处于同步水平,极低级变质作用研究等领域与国际先进水平尚有较大差距.通过历史的回顾,表明变质岩的研究已经从变质岩石学转变为变质地质学,已经从单一的岩石学研究转变为以变质岩为基础,变质矿物、地球化学、同位素地质、构造地质等多学科的综合研究.在变质岩和变质地质领域我国有一些区位优势,但是只有坚持自主创新才能把区位优势转变为学科优势.各种分析实验技术的发展促进了变质地质学的发展,随着新技术的不断涌现和大数据时代的来临,变质地质学会有更大的发展.      

变质过程中流体作用的实验研究

人们对变质过程中流体的认识是逐步深入的。最早的变质岩的研究者不认为变质过程中有流体存在。后来发现有H_2O的存在,然后又发现了CO_2。现在的研究认为变质过程中流体的成分可以非常复杂,除了H_2O和CO_2外,还有各种盐类。变质过程单独流体相存在的间接证据是通过变质岩的地球化学和岩石学研究,根据原岩与变质岩或低级变质岩与高级变质岩岩石成分的不同,经质量平衡计算得出的。足以证明变质过程中独立流体相存在的最直接的证据是各种成分的气液包裹体的存在。这些气液包裹体不仅能给出变质过程中某一点所存在流体的成分,而且有可能给出这时的温度和压力。     

高压超高压变质作用中的流体

文章强调了高压和超高压变质岩中流体包裹体的研究意义，重点论述了几个问题：（１）高压和超高压变质岩中流体包裹体的成分以含Ｎ２量高为特点，在大别山含柯石英榴辉岩中找到的高压榴辉岩阶段捕获的原生包裹体，其中气相组分含ＣＯ（摩尔分数）为１４％，表明流体来源于深部。原生流体包裹体的保存，要求在ｐ－Ｔ区间内的抬升轨迹与等容线近于平行。（２）在大别山高压和超高压榴辉岩中首次确认熔融包裹体的存在，由硅酸盐玻相和以ＣＯ２为主要成分的气相组成，并发现熔融包裹体中的玻相成分与主矿物相近。（３）高压和超高压变质期间的局部流体迁移可由榴辉岩中流体包裹体和矿物同位素成分（Ｈ－Ｃ－Ｏ）来显示。（４）高压和超高压变质中流体－熔体－岩石（矿物）相互作用是一个非常复杂的过程，并证实在榴辉岩相ｐ－Ｔ条件下岩石的部分熔融。（５）变质流体的成分与变质级之间存在着相关关系。     

绿帘石记录俯冲带变质流体活动

俯冲带是连接地球表生圈层和深部圈层的关键纽带,深刻影响着地球内部的运行方式和人类宜居环境。俯冲板片脱水释放的高压-超高压变质流体控制着俯冲带诸多重要地质过程,如地幔楔交代和部分熔融、岛弧岩浆活动、中/深源地震以及地球内部的元素迁移和分异等等。深入了解这些流体的源区、运移、成分和物理化学条件是理解这些流体性质和行为的前提和关键。绿帘石是俯冲带变质岩中一个常见的含水造岩矿物,具有较宽广的稳定温压范围(绿片岩相-榴辉岩相)、较高的微量元素含量和缓慢的体扩散行为(如Sr、Pb、Th、U、Cr、V和LREE),能够指示俯冲带(多期)变质流体活动和地球化学效应。本文总结了近年来俯冲带变质绿帘石研究的主要进展及其在揭示俯冲带流体活动方面的重要应用,包括探究俯冲带流体的起源、成分特征、运移方式、氧逸度条件、交代效应和多期次结晶行为。这些研究表明绿帘石是一个极好的变质流体活动记录器,能够为理解俯冲带流体活动和深部元素迁移提供关键信息。     

超高压变质作用不同阶段的流体变化：碧溪岭榴辉岩的氢、硼同位素分析

大别山碧溪岭榴辉岩中有三种含水矿物:多硅白云母、角闪石和黑云母,它们分别是超高压(UHP)阶段(即柯石英榴辉岩相阶段)或者石英榴辉岩相阶段、退变质后成合晶阶段和角闪岩相退变质阶段的产物,本文利用离子探针技术对它们进行了氢同位素和硼同位素的分析。三种矿物内部的同位素组成都是均一的,多硅白云母的δD为-105‰±9‰,δ~(11)B为-25.9‰±2.0‰;角闪石的δD为-100‰±9‰,δ~(11)B为-24.4‰±0.9‰;黑云母的δD为-65‰±4‰,δ~(11)B为-19.3‰±1.3‰。多硅白云母和角闪石的氢-硼同位素组成在误差范围内是相同的,而和黑云母则有明显的差别,这表明,从UHP阶段或者石英榴辉岩相阶段到随后的后成合晶阶段,变质流体是内部缓冲的,而在角闪岩相变质阶段,则有了外来流体的加入,这个流体是相对富集D和~(11)B的。碧溪岭榴辉岩矿物相对于其地壳原岩表现出低δ~(11)B的特征,说明俯冲过程中板块经历了强烈的脱硼。     

大陆板块俯冲和折返过程中的流体活动：稳定同位素证据

对大别-苏鲁造山带超高压变质岩矿物稳定同位素的系统研究发现，超高压变质过程中存在少量含水流体，但是流体的活动性很小，在不同岩相界面之间缺乏明显的流体渗透；超高压榴辉岩中的石英脉是蜂期变质后含水矿物降压分解和羟基出溶引起的流体流动结果，不是板块俯冲过程中进变质作用的产物；超高压变质岩经历了广泛的角闪岩相退变质作用，退变质流体主要来源于板块折返过程中超高压矿物中溶解经基的降压出溶。     

变质流体的内部缓冲作用和外部渗透作用

变质流体的内部缓冲作用和外部渗透作用研究是近年来变质作用研究所取得的重要进展之一．在变质作用过程中．如果变质岩石没有和外部流体源发生相互作用，变质矿物共生组合就有缓冲变质流体组成的能允这就是变质流体的内部缓冲作用；如果变质岩石受到大量的外部流体源的渗透，变质矿物组合不仅失去控制变质流体组成的能力，而且要调整自身组成．以便与外部流体组成保持化学平衡，这就是流体的外部渗透作用．变质流体的内部缓冲和外都渗透代表了自然所发生的两种极端现象．变质作用过程中更为普遍现象是变质流体既受内部经冲控制又受外部渗透控制．     

滇西北铜厂沟Mo-Cu矿床成矿流体和成矿物质来源:矽卡岩矿物学与稳定同位素证据

义敦地体位于三江特提斯成矿域中北段,晚三叠世和晚白垩世斑岩-矽卡岩型Mo-Cu多金属成矿作用强烈。铜厂沟Mo-Cu矿床位于义敦地体最南端,是近年来该区新探明的Mo-Cu矿床之一,已探明资源量142.5Mt。矽卡岩在铜厂沟矿区广泛出露,是该矿区最主要的赋矿岩石。根据矿物组合及共生关系,可将矽卡岩划分为石榴子石矽卡岩、透辉石矽卡岩和透闪石矽卡岩三种类型。通过详细的地质填图和钻孔岩心编录,发现铜厂沟矿区矽卡岩矿物组合受花岗闪长斑岩体与大理岩空间分布的控制:(1)由大理岩向外依次发育透辉石矽卡岩→透闪石矽卡岩→石榴子石矽卡岩;(2)由浅至深,石榴子石粒度逐渐变大;③矿化与透闪石、绿帘石等退化蚀变矿物密切相关,矿体多形成于外接触带。矽卡岩中最主要的矿物是石榴子石,多呈自形粒状或粒状集合体产出,颜色较深,均质性,以钙铝榴石为主(62.2%~78.3%),其次为钙铁榴石(16.7%~34.2%),少量锰铝榴石、铁铝榴石和镁铝榴石,属于钙铝榴石-钙铁榴石固溶体系列(Gro62-78And17-34Spe+Pyr+Alm2-6)。石榴子石Fe~(2+)/Fe~(3+)比值变化范围为0.00~0.20,平均值为0.06,指示石榴子石形成于酸性的氧化环境。石榴子石的δ~(18)OSMOW变化范围为5.2‰~9.5‰,反映矽卡岩可能直接继承斑岩体的氧同位素组成;金属硫化物具有较为均一的S-Pb同位素范围(δ~(34)S(CDT)=-0.7‰~1.4‰;~(206)Pb/~(204)Pb=18.332~18.694,~(208)Pb/~(204)Pb=38.454~39.088,~(207)Pb/~(204)Pb=15.588~15.663),表明成矿流体和成矿物质均来源于壳源的长英质岩浆。     

The role of fluids in faulting deformation:a case study from the Dead Sea Transform (Jordan)

The geochemistry of carbonate fault rocks has been examined in two areas of the Arava Fault segment, which forms the major branch of the Dead Sea Transform between the Dead Sea and the Gulf of Aquaba. The role of fluids in faulting deformation in the selected fault segment is remarkably different from observations at other major fault zones. Our data suggest reduced fluid rock interactions in both areas and limited fluid flow. The fault did not act as an important fluid conduit. There are no indications that hydrothermal reactions (cementation, dissolution) did change the strength and behavior of the fault zone, although the two areas show considerable differences with respect to fluid sources and fluid flow. In one area, the investigated calcite mineralization reveals an open fluid system with fluids originating from a variety of sources. Stable isotopes (¹³C, ¹⁸O), strontium isotopes, and trace elements indicate both infiltration of descending (meteoric and/or sea water) and ascending hydrothermal fluids. In the other area, all geochemical data indicate only local (small scale) fluid redistribution. These fluids were derived from the adjacent limestones under nearly closed-system conditions.     

Boron isotopic composition of subduction-zone metamorphic rocks

Many arc lavas contain material derived from subducted oceanic crust and sediments, but it remains unresolved whether this distinctive geochemical signature is transferred from the subducting slab by aqueous fluids, silicate melts, or both. Boron isotopic measurements have the potential to distinguish between slab transfer mechanisms because ¹¹B fractionates preferentially into aqueous fluids whereas little fractionation may occur during partial melting. Previous studies have shown that δ¹¹B values of island arc lavas (−6 to +7) overlap the range of δ¹¹B values for altered oceanic crust (−5 to +25) and pelagic sediments and turbidites (−7 to +11). Secondary ion mass spectrometry (SIMS) analyses of minerals in subduction-zone metamorphic rocks yield δ¹¹B=−11 to −3 suggesting that slab dehydration reactions significantly lower the δ¹¹B values of subducted oceanic crust and sediments. In order to explain the higher δ¹¹B values reported for arc lavas as compared to subduction-zone metamorphic rocks, the B-bearing component derived from the metamorphosed slab must be enriched in ¹¹B relative to the slab, favoring an aqueous fluid as the slab transfer mechanism.     

Evolution of fluids associated with metasedimentary sequences from Chaves (North Portugal)

In order to identify and characterise fluids associated with metamorphic rocks from the Chaves region (North Portugal), fluid inclusions were studied in quartz veinlets, concordant with the main foliation, in graphitic-rich and nongraphitic-rich lithologies from areas with distinct metamorphic grade. The study indicates multiple fluid circulation events with a variety of compositions, broadly within the C–H–O–N–salt system. Primary fluid inclusions in quartz contain low salinity aqueous–carbonic, H₂O–CH₄–N₂–NaCl fluids that were trapped near the peak of regional metamorphism, which occurred during or immediately after D2. The calculated P–T conditions for the western area of Chaves (CW) is P=300–350 MPa and T500 °C, and for the eastern area (CE), P=200–250 MPa and T=400–450 °C. A first generation of secondary fluid inclusions is restricted to discrete cracks at the grain boundaries of quartz and consists of low salinity aqueous–carbonic, H₂O–CO₂–CH₄–N₂–NaCl fluids. P–T conditions from the fluid inclusions indicate that they were trapped during a thermal event, probably related with the emplacement of the two-mica granites.

A second generation of secondary inclusions occurs in intergranular fractures and is characterised by two types of aqueous inclusions. One type is a low salinity, H₂O–NaCl fluid and the second consists of a high salinity, H₂O–NaCl–CaCl₂ fluid. These fluid inclusions are not related to the metamorphic process and have been trapped after D3 at relatively low P (hydrostatic)–T conditions (P<100 MPa and T<300 °C).

Both the early H₂O–CH₄–N₂–NaCl fluids in quartz from the graphitic-rich lithologies and the later H₂O–CO₂–CH₄–N₂–NaCl carbonic fluid in quartz from graphitic-rich and nongraphitic-rich lithologies seem to have a common origin and evolution. They have low salinity, probably resulting from connate waters that were diluted by the water released from mineral dehydration during metamorphism. Their main component is water, but the early H₂O–CH₄–N₂–NaCl fluids are enriched in CH₄ due to interaction with the C-rich host rocks.

From the early H₂O–CH₄–N₂–NaCl to the later aqueous–carbonic H₂O–CO₂–CH₄–N₂–NaCl fluids, there is an enrichment in CO₂ that is more significant for the fluids associated with nongraphitic-rich lithologies.

The aqueous–carbonic fluids, enriched in H₂O and CH₄, are primarily associated with graphitic-rich lithologies. However, the aqueous–carbonic CO₂-rich fluids were found in both graphitic and nongraphitic-rich units from both the CW and CE studied areas, which are of medium and low metamorphic grade, respectively.     

3D numerical modelling of fluid flow in the Val-d’Or orogenic gold district: major crustal shear zones drain fluids from overpressured vein fields

Fluid flow patterns have been determined using oxygen isotope isopleths in the Val-d’Or orogenic gold district. 3D numerical modelling of fluid flow and oxygen isotope exchange in the vein field shows that the fluid flow patterns can be reproduced if the lower boundary of the model is permeable, which represents middle or lower crustal rocks that are infiltrated by a metamorphic fluid generated at deeper levels. This boundary condition implies that the major crustal faults so conspicuous in vein fields do not act as the only major channel for upward fluid flow. The upper model boundary is impermeable except along the trace of major crustal faults where fluids are allowed to drain out of the vein field. This upper impermeable boundary condition represents a low-permeability layer in the crust that separates the overpressured fluid from the overlying hydrostatic fluid pressure regime. We propose that the role of major crustal faults in overpressured vein fields, independent of tectonic setting, is to drain hydrothermal fluids out of the vein field along a breach across an impermeable layer higher in the crust and above the vein field. This breach is crucial to allow flow out of the vein field and accumulation of metals in the fractures, and this breach has major implications for exploration for mineral resources. We propose that tectonic events that cause episodic metamorphic dehydration create a short-lived pulse of metamorphic fluid to rise along zones of transient permeability. This results in a fluid wave that propagates upward carrying metals to the mineralized area. Earthquakes along crustal shear zones cause dilation near jogs that draw fluids and deposit metals in an interconnected network of subsidiary shear zones. Fluid flow is arrested by an impermeable barrier separating the hydrostatic and lithostatic fluid pressure regimes. Fluids flow through the evolving and interconnected network of shear zones and by advection through the rock matrix. Episodic breaches in the impermeable barrier along the crustal shear zones allow fluid flow out of the vein field.     

Compositionally zoned Cl-rich amphiboles from North Dabie Shan, China: monitor of high-pressure metamorphic fluid/rock interaction processes

Amphiboles containing up to 4.2 wt.% Cl are found in felsic granulites from Yanzihe within the North Dabie area of the Dabie–Sulu ultrahigh- and high-pressure metamorphic belt in eastern China. Most amphibole grains show considerable zonations with Cl contents ranging from 0 to 4.2 wt.%. Based on their textural features, amphiboles can be divided into four generations: (1) amphibole occurring as inclusions in orthopyroxene (Am-in) with Cl contents around 3.5 wt.%; (2) amphibole forming cores of grains in the matrix (AM-I) with Cl contents between 3.0 and 4.2 wt.%; (3) amphibole with Cl contents of 0.2 to 2.5 wt.% (Am-II) occurring as hydrothermally altered parts of the original amphibole; (4) Cl-free amphibole (Am-III) usually developed at the outermost rim of the grain. Major and rare earth elements show significant variations for Am-I, Am-II and Am-III.

Different generations of amphiboles are related to different metamorphic stages of the granulite in Yanzihe, and provide a monitor for fluid/rock interactions and P–T evolution during the high-pressure metamorphism of Dabie Shan. Pressure and temperature estimates suggest that Am-in was formed during prograde metamorphism of 10 kbar and 700–800 °C; Am-I was formed under peak metamorphic conditions (20 kbar, 800–960 °C), whereas Am-II and Am-III were formed during retrograde metamorphic stages (560–770 °C and 5–7 kbar, and 520–670 °C and <5 kbar, respectively). In contrast to most previous studies, in which the earliest amphiboles to form are typically Cl-poor and later amphiboles become progressively Cl-rich, we show that the earliest amphiboles in the investigated rock are Cl-rich and later formed amphiboles are Cl-poor. The present study also demonstrates that the fluid system of the granulites in North Dabie Shan did not evolve in a simple way: while it behaved as a closed system during prograde and peak metamorphism, after the metamorphic peak it probably acted as an open system in which new fluids were introduced. The varying magnitude of Cl contents in amphiboles stresses the very local fluid control during metamorphism.     

胶东石城金矿床成矿流体特征及成矿作用

石城金矿位于胶东牟平-乳山成矿带南端,为多金属硫化物型金矿床。其成矿流体阶段可分为3个,相应的流体包裹体特征为:(1)成矿早期(第1阶段)富CO2包裹体;(2)主成矿期(第2阶段)H2O包裹体和含CO2包裹体;(3)成矿后期(第3阶段)H2O包裹体。第1阶段均一温度为256～360℃,盐度3.71%～6.88%NaCl,第2阶段均一温度为168～270℃,盐度4.49%～10.24%NaCl,第3阶段均一温度为123～178℃,盐度0.35%～7.59%NaCl。其中主成矿期为中低温、低盐度的CO2-H2O-NaCl流体体系。H、O同位素表明石城金矿成矿流体为岩浆水与大气水形成的混合热液,C、O同位素则反映了地幔富CO2流体参与了成矿作用,而S同位素进一步揭示了金矿的成矿物质来源为壳幔相互作用的结果。石城金矿的出现表明研究区至少存在两期成矿事件,早期成矿时代约120Ma,主要为石英+黄铁矿型矿石,晚期成矿时代小于111Ma,主要为多金属硫化物型矿石,以石城金矿为代表。     

The Paleoproterozoic carbonate-hosted Pering Zn–Pb deposit, South Africa. II: fluid inclusion, fluid chemistry and stable isotope constraints

The Pering deposit is the prime example of Zn–Pb mineralisation hosted by stromatolitic dolostones of the Neoarchean to Paleoproterozoic Transvaal Supergroup. The hydrothermal deposit centers on subvertical breccia pipes that crosscut stromatolitic dolostones of the Reivilo Formation, the lowermost portion of the Campbellrand Subgroup. Four distinct stages of hydrothermal mineralisation are recognised. Early pyritic rock matrix brecciation is followed by collomorphous sphalerite mineralisation with replacive character, which, in turn, is succeeded by coarse grained open-space-infill of sphalerite, galena, sparry dolomite, and quartz. Together, the latter two stages account for ore-grade Zn–Pb mineralisation. The fourth and final paragenetic stage is characterised by open-space-infill by coarse sparry calcite. The present study documents the results of a detailed geochemical study of the Pering deposit, including fluid inclusion microthermometry, fluid chemistry and stable isotope geochemistry of sulphides (δ³⁴S) and carbonate gangue (δ¹³C and δ¹⁸O). Microthermometric fluid inclusion studies carried out on a series of coarsely grained crystalline quartz and sphalerite samples of the latter, open-space-infill stage of the main mineralisation event reveal the presence of three major fluid types: (1) a halite–saturated aqueous fluid H₂O–NaCl–CaCl₂ (>33 wt% NaCl equivalent) brine, (2) low-salinity meteoric fluid (<7 wt% NaCl) and (3) a carbonic CH₄–CO₂–HS⁻ fluid that may be derived from organic material present within the host dolostone. Mixing of these fluids have given rise to variable mixtures (H₂O–CaCl₂–NaCl ±(CH₄–CO₂–HS⁻), 2 to 25 wt% NaCl+CaCl₂). Heterogeneous trapping of the aqueous and carbonic fluids occurred under conditions of immiscibility. Fluid temperature and pressure conditions during mineralisation are determined to be 200–210°C and 1.1–1.4 kbar, corresponding to a depth of mineralisation of 4.1–5.2 km. Chemical analyses of the brine inclusions show them to be dominated by Na and Cl with lesser amounts of Ca, K and SO₄. Fluid ratios of Cl/Br indicate that they originated as halite saturated seawater brines that mixed with lower salinity fluids. Analyses of individual brine inclusions document high concentrations of Zn and Pb (∼1,500 and ∼200 ppm respectively) and identify the brine as responsible for the introduction of base metals. Stable isotope data were acquired for host rock and hydrothermal carbonates (dolomite, calcite) and sulphides (pyrite, sphalerite, galena and chalcopyrite). The ore-forming sulphides show a trend to ³⁴S enrichment from pyrite nodules in the pyritic rock matrix breccia (δ³⁴S = −9.9 to +3.7‰) to paragenetically late chalcopyrite of the main mineralisation event (δ³⁴S = +30.0‰). The observed trend is attributed to Rayleigh fractionation during the complete reduction of sulphate in a restricted reservoir by thermochemical sulphate reduction, and incremental precipitation of the generated sulphide. The initial sulphate reservoir is expected to have had an isotopic signature around 0‰, and may well represent magmatic sulphur, oxidised and leached by the metal-bearing brine. The δ¹⁸O values of successive generations of dolomite, from host dolostone to paragenetically late saddle dolomite follow a consistent trend that yields convincing evidence for extensive water rock interaction at variable fluid–rock ratios. Values of δ¹³C remain virtually unchanged and similar to the host dolostone, thus suggesting insignificant influx of CO₂ during the early and main stages of mineralisation. On the other hand, δ¹³C and δ¹⁸O of post-ore calcite define two distinct clusters that may be attributed to changes in the relative abundance in CH₄ and CO₂ during waning stages of hydrothermal fluid flow.     

高盐变质流体对我国绿岩带金矿的制约

高盐变质流体为绿岩带原岩在变质 -混合岩化过程中产生的液体 ,其含盐度高达 30～ 40 wt% Na Cl,富含 K、Na、Ca、Mg碱金属离子 ,K/ Na≈ 1,呈强碱性 ,有利于绿岩中 Au的活化和迁移 ,使绿岩带起到金的矿源层作用 ,并且间接地控制了变质期后绿岩型金矿的形成和分布 ,控制了绿岩型金矿的规模大小     

Fluid venting activity on the Costa Rica margin: new results from authigenic carbonates

Carbonate precipitates on mounds and along tectonic scarps off the Costa Rica margin are manifestations of subduction-induced dewatering. The long-term dewatering history is recorded in mineralogical, petrological and isotope signals of carbonates recovered from these sites. The carbonates are strongly depleted in ¹³C (–11 to –53 PDB) and enriched in ¹⁸O (+4 to +8 PDB). Thermogenic methane and biogenic methane were identified as sources of the carbon. Chemoherm carbonates and seepage-associated carbonates formed in a focused flow regime have lighter ¹³C values, while others formed in a more diffusive flow regime have slightly enriched C isotope values. Three fluid components were inferred based on the calculation of equilibrium ¹⁸O: clay dehydration water, gas hydrate water and seawater. Calculated equilibrium ¹⁸O values of carbonates from different down-core depths as well as from different precipitation stages show that the ¹⁸O of the precipitating fluid is progressively depleted with time. Dolostones showing a methane-C source and a well constrained O-isotope signature are thought to have formed at depth in the sediment and subsequently became exhumed. Glauconitic sandstones cemented by methane-derived carbonate provide evidence that fluid and solid material have been expelled by the mud volcano.