Rare Earth Element Behaviour in the Wunugetushan Copper – Molybdenum Deposit,Inner Mongolia,and Its Implications1

Abstract Considering porphyry and wall rocks as a whole system, the behaviour of rare earth elements (REE) in hydro thermal alteration and mineralization of the exceedingly large Wunugetushan porphyry Cu-Mo deposit of Inner Mongolia has been studied. It has been found for the first time that there exists complementary REE variation in hydrothermal alteration between porphyry and wall rocks, and Eu depletion has certain significance in indicating mineralization. Based on an analysis of the variation in REE contents of relevant minerals during the hydrothermal alteration, the ore-forming fluids are inferred to be depleted in ∑REE, comparatively enriched in ∑Y and strongly depleted in Eu. In the intermediate-strong alteration zones, porphyry and wall rock took part in hydrothermal metasomatism and alteration almost in equal ratio mass. Furthermore, studies of REE and hydrogen and oxygen isotopes and fluid inclusions confirm the existence of hydrothermal convection and the possibility of supplying part of ore materials by the wall rock and indicate that the application of REE geochemistry in mineral prospecting is promising.     

Numerical Simulation of Fluid Migration during Ore Formation of Carboniferous Exhalation-Sedimentary Massive Sulfide Deposits in the Tongling District, Anhui Province

Numerical simulation of fluid migration during the ore-forming process of the Carboniferous exhalationsedimentary (Sedex) massive sulfide deposits in the Tongling district shows that fluid and thermal activities in lying-wall rocks were limited to a small area around the main draining passage, which led to weak mineralization and alteration in the lying-wall rock. Temperature and fluid fields indicate that mineralization and alteration in the lying-wall rock of the Sedex-type deposits are usually weaker than those of volcano-hosted massive sulfide deposits. Fluid migration involves the following processes: seawater penetrating and leaching the lying-wall rocks, then mixing with ascending hydrothermal fluids in the main draining passage, and finally jetting into seafloor. Although fluid activity-influenced area is rather small,the content of metals leached out from the lying-wall rocks is high enough to form large-scale ore deposits. Tensional contemporaneous faults accompanied with strong heat flows controlled the formation and distribution of Sedex deposits.The tensional tectonic regime on the northern margin of the Yangtze block during the Hercynian provided Sedex deposits with a prerequisite geodynamic condition.     

相山铀矿田成矿流体特征:来自微量、稀土元素地球化学证据

相山铀矿田的成矿流体性质和来源存在争议,为进一步探讨相山铀矿田成矿流体的性质和来源,本文对相山铀矿田西部的居隆庵铀矿床和北部的沙洲铀矿床中的新鲜围岩、蚀变围岩及矿石的微量、稀土元素含量及其变化进行了研究。结果显示:在含较多热液成因萤石的居隆庵铀矿床中,从新鲜围岩到蚀变围岩到矿石,Zr、Hf含量先降低再升高;而在含少量热液萤石的沙洲铀矿床中,新鲜围岩、蚀变围岩和矿石的Zr、Hf含量基本一致。鉴于富F流体易汲取岩石中的Zr、Hf,因此,这两个矿床中不同类型样品Zr、Hf含量的不同变化趋势,可能与居隆庵铀矿床的成矿流体富F、而沙洲铀矿床的成矿流体相对贫F有关。这两个铀矿床中矿石的稀土配分曲线与其各自的新鲜及蚀变围岩的稀土配分曲线形态相似但又存在差异,说明每个矿床的新鲜围岩、蚀变围岩和矿石之间的稀土元素既具有继承性、又受到不同性质的流体的影响。居隆庵铀矿床中矿石显示Eu负异常,可能主要是继承了围岩的Eu负异常;沙洲铀矿床中矿石Eu显示弱负异常至弱正异常的特征,可能与围岩中斜长石因热液蚀变作用而释放出的Eu的进入流体有关。基于新鲜围岩、蚀变围岩及矿石的U和REE研究,推断居隆庵铀矿床成矿流体中U和REE均以F的络合物形式迁移;但沙洲铀矿床中铀矿石品位较低,可能是与流体中相对贫F有关。     

青海茫崖石棉矿区变质超基性岩的蚀变演化序列：岩石化学及矿物学证据

青海茫崖石棉矿区超基性岩体是由原岩以纯橄岩、辉橄岩和橄辉岩为主体组成的富镁质超基性岩体,经历自变质和后期多期热液的叠加变质蚀变作用,经蛇纹石化后形成蚀变完全的蛇纹岩岩体,其中部分蛇纹岩又进一步发生滑石化及碳酸盐化蚀变为滑石菱镁片岩、菱镁滑石片岩、滑石片岩和菱镁岩等。本文在野外地质调查基础上,在室内通过镜下岩矿综合鉴定、全岩化学成分分析以及电子探针成分分析等手段进行了岩石化学特征、矿物学特征及其蚀变演化过程研究。结果表明,该变质超基性岩体蛇纹岩主要特征组合矿物为蛇纹石(利蛇纹石、叶蛇纹石、纤蛇纹石)、磁铁矿、菱镁矿、滑石、水镁石、铬铁矿,变余矿物有斜方辉石、单斜辉石和铬铁矿,滑石菱镁片岩类主要组成矿物为菱镁矿、滑石、蛇纹石及磁铁矿,局部可见石英脉。该地区变质超基性岩体较完整地记录了橄榄岩水化、滑石化及碳酸盐化作用过程的各个阶段,超基性岩蚀变演化过程主要有两个作用阶段:(Ⅰ)橄榄石、辉石类矿物的蛇纹石化作用及蛇纹石绿泥石化作用;(Ⅱ)富Ca、CO2流体交代蛇纹石、滑石及水镁石的碳酸盐化作用。蛇纹石化等变质蚀变作用促进了Si、Mg及Fe元素化学活动性,使元素发生富集与迁移,对于次生矿物的形成与演化起到了一定的催化作用。多期不同组成流体热液的交代作用过程,清晰地展示了利蛇纹石、纤蛇纹石和叶蛇纹石的演化序列,以及滑石、水镁石、铬铁矿和磁铁矿的形成过程及标形特征。     

内蒙古喀喇沁旗安家营子金矿蚀变及其分布研究

位于华北克拉通北缘的安家营子金矿是一赋存在花岗岩中的复合型金矿,既有石英脉型矿化,也有蚀变岩型矿化,矿区发育广泛的热液蚀变。本文在详细的矿床地质特征研究基础上,通过系统采样、镜下鉴定,详细研究了安家营子金矿蚀变岩的类型、矿物组合、空间分布以及地球化学特征,探讨了蚀变岩的分带性、成矿流体的演化等。结果表明,安家营子金矿主要受NNE向脆性断裂的控制,蚀变岩即分布在断裂的影响范围内。主要的蚀变类型有钠长石化、绢云母化、绿泥石化、硅化和黄铁绢英岩化等,其中钠长石化在整个矿区均有分布,其余蚀变则分散在不同的独立区域。热动力学数据表明,安家营子金矿早期成矿流体K^+含量不高,可能相对富Na^+,因此钠长石化大量出现;随着钠长石的大量形成,流体成分演化至绢云母和钾长石的稳定范围,并出现绢云母化,但钾长石保持稳定。随着流体进一步演化至绢云母的稳定范围,绢英岩化开始大量出现,并且斜长石和钾长石基本消失,形成矿区主要的蚀变岩型矿体。安家营子金矿形成于喀喇沁变质核杂岩快速隆升期,因此控矿的次级脆性断裂构造的性质在拉张和剪切之间波动,导致蚀变分带不明显,也使得脉状矿化和蚀变岩型矿化叠加在一起。     

The mineral chemistry of hydrothermally altered and metamorphosed wall-rocks at the Stollberg Fe-Pb-Zn-Mn(-Ag) deposit,Bergslagen, Sweden

The c. 1.9 Ga old Stollberg sulphide and Mnrich skarn iron ores and sulphide ores in Bergslagen, south-central Sweden are hosted by hydrothermally altered and metamorphosed felsic volcanic and volcaniclastic rocks. The ores are underlain by comformable alteration zones characterized by albite-gedrite-quartz and biotite-muscovite-plagioclase-K-feldspar-quartz +/– garnet assemblages. The present mineralogies are interpreted as medium-grade metamorphic equivalents to the original alteration mineral assemblages. PT-conditions during prograde regional metamorphism are semiquantatively determined to be 510 to 560 °C at approximately 3 kbar. With increasing modal content of gedrite and biotite in the alteration zones, the Mg/Fe ratios and X_Mg's in octahedral positions of these minerals also increase. In the gedrite-bearing strata, whole-rock Mg/Fe ratios remain constant, whereas in the biotite-rich unit the wholerock Mg/Fe trend is parallel to that of the biotites.The trends in the metamorphic mineral composition are interpreted to be a product of original changes in fluid composition during the evolution of a sub-seafloor hydrothermal system. During the initial stage of alteration, Fe-Mn-rich fluids altered the rocks, and during a later stage, the fluids became more Mg-rich, possibly due to entrainment of fresh seawater, and the alteration zones became relatively more Mg-rich. Sulphide precipitation was contemperaneous with Mg metasomatism, suggesting base metal precipitation was a function of the mixing of cool seawater with hydrothermal fluid. It is proposed that early hydrothermal alteration was associated with the deposition of areally extensive Fe-oxide formation, and that Mg metasomatism defines a second stage of hydrothermal activity during which sulphide mineralization overprinted the earlier formed Fe-oxide deposit.     

Hydrothermal alterations in the Echassières granitic cupola (Massif central,france)

Detailed petrographic and mineralogic investigations of an albite-lepidolite granite at Echassières (Massif Central, France; scientific deep drill program) shows the existence of hydrothermal stages which are closely related to the magmatic and structural history. According to fluid inclusion data, K-Ar datations and ¹⁸O/¹⁶O-D/H compositions of secondary minerals, two successive hydrothermal periods have been recognized. The early one (273–268 million years) produced a series of aluminous phyllosilicates: muscovite, pyrophyllite, donbassite, tosudite, kaolinite which are observed as vein deposits (<10 mm wide) and alteration products of primary minerals in wall-rocks. The vein system was sealed by monomineralic assemblages during a cooling period (400–150°C). This early hydrothermal alteration stage was controlled by interactions of rock with low salinity (1–10 wt% NaCl equivalent) fluids expelled from the granitic body during the cooling processes. The chemical properties of these fluids were the following: low pH, very low Mg and Fe and high Li, Na and K contents. Thermodynamic calculations show that the sequence pyrophyllite, Li-bearing donbassite, tosudite is mostly temperature dependent. From the chemical composition of secondary minerals and isotopic data it can be deduced that these fluids, which have a meteoric origin, have been expelled from the granite body during its cooling period and after interaction with it at high temperature. The late hydrothermal stage corresponds to deposits of fluorite and Fe-Mg rich illite (151 million years) in subvertical fractures. Temperature conditions did not exceed 250° C and fluids came through the surrounding metamorphic rocks into the granitic body. IIlite/smectite mixed-layer minerals have been identified in subvertical fractures which were opened during Tertiary periods. In the host micaschists, successive hydrothermal alterations took place during the cooling of the Beauvoir granite. Early magmatic fluids interacted with these micaschists. Locally, the metamorphic assemblage is replaced by a metasomatic one. Secondary topaz and (F, Li)-rich mica crystals were formed over a range of 450 of 150°C. Later hydrothermal fluids reacted with the country rocks to form phengite-biotite, chlorite-illite and kaolinite over a range of 300 to 150°C. Illite/smectite mixed-layer minerals crystallized in the roof micaschists and within the Beauvoir granite during the Tertiary alteration period. Meteoric water invaded open fractures producing supergene alteration mineral assemblages.     

Fluid elemental and stable isotope composition of the Nibelungen hydrothermal field (8°18′S,Mid-Atlantic Ridge): Constraints on fluid–rock interaction in heterogeneous lithosphere

Depending on the geological setting, the interaction of submarine hydrothermal fluids with the host rock leads to distinct energy and mass transfers between the lithosphere and the hydrosphere. The Nibelungen hydrothermal field is located at 8°18′S, about 9 km off-axis of the Mid-Atlantic Ridge (MAR). At 3000 m water depth, 372 °C hot, acidic fluids emanate directly from the bottom, without visible sulfide chimney formation. Hydrothermal fluids obtained in 2009 are characterized by low H₂S concentrations (1.1 mM), a depletion of B (192 μM) relative to seawater, lower Si (13.7 mM) and Li (391 μM) concentrations relative to basaltic-hosted hydrothermal systems and a large positive Eu anomaly, and display a distinct stable isotope signature of hydrogen (?²H_H2O = 7.6–8.7‰) and of oxygen (?¹⁸O_H2O = 2.2–2.4‰).The heavy hydrogen isotopic signature of the Nibelungen fluids is a specific feature of ultramafic-hosted hydrothermal systems and is mainly controlled by the formation of OH-bearing alteration minerals like serpentine, brucite, and tremolite during pervasive serpentinization. New isotopic data obtained for the ultramafic-hosted Logatchev I field at 14°45′N, MAR (?²H_H2O = 3.8–4.2‰) display a similar trend, being clearly distinguished from other, mafic-hosted hydrothermal systems at the MAR.The fluid geochemistry at Nibelungen kept stable since the first sampling campaign in 2006 and is evident for a hybrid alteration of mafic and ultramafic rocks in the subseafloor. Whereas the ultramafic-fingerprint parameters Si, Li, B, Eu anomaly and ?²H_H2O distinguish the Nibelungen field from other hydrothermal systems venting in basaltic settings at similar physico-chemical conditions and are related to the interaction with mantle rocks, the relatively high concentrations of trace alkali elements, Pb, and Tl can only be attributed to the alteration of melt-derived gabbroic rocks. The elemental and isotopic composition of the fluid suggest a multi-step alteration sequence: (1) low- to medium-temperature alteration of gabbroic rocks, (2) pervasive serpentinization at moderate to high temperatures, and (3) limited high-temperature interaction with basaltic rocks during final ascent of the fluid. The integrated water/rock ratio for the Nibelungen hydrothermal system is about 0.5.The fluid compositional fingerprint at Nibelungen is similar to the ultramafic-hosted Logatchev I fluids with respect to key parameters. Some compositional differences can be ascribed to different alteration temperatures and other fluid pathways involving a variety of source rocks, higher water/rock ratios, and sulfide precipitation in the sub-seafloor at Logatchev I.     

Alteration of the oceanic crust: Implications for geochemical cycles of lithium and boron

Fresh tholeiitic basalt glass has been reacted with seawater at 150°C, (water/rock mass ratio of 10), and fresh diabase has been reacted with a Na-K-Ca-Cl fluid at 375°C (water/rock mass ratios of 1, 2, and 5) to understand better the role of temperature, basalt composition, and water/rock mass ratio on the direction and magnitude of B and Li exchange during basalt alteration. At 150°C, slight but nevertheless significant amounts of B and Li were removed from seawater and incorporated into a dominantly smectite alteration phase. At 375°C, however, B and Li were leached from basalt. B behaved as a “soluble” element and attained concentrations in solution limited only by the B concentration in basalt and the water/rock mass ratio. Li, however, was less mobile. For example, at water/rock mass ratios of 1, 2, and 5, the percent of Li leached from basalt was 58, 70, and 92% respectively. This suggests some mineralogic control on Li mobility during hydrothermal alteration of basalt, especially at low-water/rock mass ratios. In general, these results, as well as those for B, are consistent with the temperature-dependent chemistry of altered seafloor basalt and the chemistry of ridge crest hydrothermal fluids.Based on the distribution and chemistry of products of seafloor weathering, low (≤ 150°C) and high-temperature hydrothermal alteration of basalt, and the chemistry of ridge crest hydrothermal fluids, it was estimated that alteration of the oceanic crust is a Li source for seawater. This is not true for B, however, since the hot spring flux estimated for B is balanced by low-temperature basalt alteration. These data, coupled with B and Li flux estimates for other processes (e.g., continental weathering, clay mineral adsorption, authigenic silicate formation and formation of siliceous skeletal material) yield new insight into the B and Li geochemical cycles. Calculations performed here indicate relatively good agreement between the magnitude of B and Li sources and sinks. The geochemical cycle of B, however, may be affected by serpentinization of mantle derived peridotite in oceanic fracture zones. Serpentinites are conspicuously enriched in B and if the B source for these rocks is seawater, then an additional B sink exists which must be integrated into the B geochemical cycle. However, until more data are available in terms of areal extent of serpentinization, serpentite chemistry and isotopic composition, the importance of B in these rocks with respect to the B geochemical cycle remains speculative at best.     

The genesis of Zr–Nb–REE mineralisation at Khalzan Buregte (Western Mongolia) reconsidered

The sources and formation conditions of unconventional Zr–Nb–REE mineralisation (REE = rare earth elements) presently found in increasing number worldwide are still poorly constrained. One particular problem is the specific role of magmatic and hydrothermal processes active in various geological settings. Investigation of Zr–Nb–REE mineralisation at Khalzan Buregte and Tsakhir, Western Mongolia, enables to evaluate magmatic processes preceding economic mineralisation and, in a second step, to compare similar ore-forming processes developing in host rocks of contrasting rock composition (low- vs. high-silica rocks). The genesis of the Zr–Nb–REE mineralisation is re-assessed using field observations, whole rock analysis (chemical composition, quantitative modal analysis by X-ray diffraction) and by the application of various transmitted light and electron microscopic techniques. Coarse-grained intrusive bodies, dikes and volcanic rocks of alkaline, silica-saturated composition were found to be contemporarily emplaced at subvolcanic to volcanic levels forming four alkaline massifs within the Khalzan Buregte area. The whole rock composition of weakly altered magmatic rocks ranges from syenite to quartz monzonite and alkaline granite (alkali feldspar syenite to alkali feldspar granite according to their modal composition). Magmatic and at least two subsequent hydrothermal processes contributed significantly to the formation of economic concentrations of high field strength elements (HFSE) such as Zr, Hf, Nb, Ta, REE and Y in the Khalzan Buregte deposit and in the nearby Tsakhir prospect. Mixing of magma from at least three sources and the formation of potassium feldspar cumulates resulted in local enrichment of Zr, Nb and light rare earth elements (LREE) in the rocks up to sub-economic levels. There was no significant increase in Y and heavy rare earth elements (HREE) during magmatism.Multistage metasomatic alteration resulted in a pronounced chemical and mineralogical heterogeneity of associated alteration assemblages. The main hosts of Zr and Hf in the ores are zircon and other zirconium silicates (gittinsite, catapleiite-(Ca) and elpidite). The rare metals Nb and Ta are mainly contained in various types of pyrochlore (Khalzan Buregte) and, to a lesser extent, in fergusonite and other minerals (Tsakhir). A large variety of REE- and Y-bearing minerals have been identified, including oxides, fluorocarbonates and silicates. Early hydrothermal alteration by silica- and carbonate-rich fluids yielded extreme concentrations of Zr, Nb and LREE. Later alteration resulted in enrichment of Y and HREE. In the latter case, fluids were very rich in fluorine. Our preliminary genetic model assumes a carbonatite-related fluid system responsible for the early alteration that occurred late during or postdating the intrusion/extrusion of the silica-saturated magmas. A “Li-F granite-type” fluid system was active during the late alteration. The interplay of all these processes resulted in the formation of a complex, economic Zr–Nb–REE mineralisation at Khalzan Buregte.     

Fluid metasomatic genesis of stratiform skarn in the Suoerkuduke Cu-Mo deposit,East Junggar,NW China

Stratiform skarns associated with ore deposits are widespread in the north of East Junggar, particularly in the Suoerkuduke Cu-Mo deposit. The Suoerkuduke stratiform and stratoid skarns are hosted by Devonian intermediate-mafic volcanic and pyroclastic rocks, mainly andesite, andesitic porphyry and tuffaceous sandstone, without carbonate or calcareous rocks. The skarns consist of dominant andradite-grossular, epidote, diopside-hedenbergite and minor actinolite, quartz, magnetite and metallic sulfides. The garnet and epidote composition, especially Fe^3 + and Al contents, is largely a function of the bulk composition and physicochemical environment (particularly fO₂) during crystallization. Such mineralogy indicates a relatively oxidizing environment and medium acidity of solution during skarnization.The Suoerkuduke skarns are distinct from typical contact metasomatic skarn in wall rock, as no carbonate or calcareous rocks were found, and differ in the distribution patterns of skarn zonation in that gradually weakened skarn zones are not quite symmetrically distributed on both sides of the alteration center (a garnet skarn). Abundant remnants of andesite, andesitic porphyry and tuffaceous sandstone in the weakened skarn zone indicate that the protolith of the skarn is andesite, andesitic porphyry and tuffaceous sandstone. Magmatic water, meteoric and seawater are involved in skarn alteration. Moyite and granitic porphyry are not coeval with skarn, and their emplacement resulted in the hornfelization of wall rock instead of skarnization, and themselves keep away from skarn alteration. Therefore, there was probably a huge batholith supplying magmatic fluid for skarn formation. Mass balance estimates suggest that hydrothermal fluid must contribute a portion of Ca and Fe to ensure sufficient supply for skarn formation in the absence of local carbonate and calcareous rocks. In conclusion, the stratiform skarns in the Suoerkuduke are products of intermediate-mafic volcanic and pyroclastic rocks metasomatised by hydrothermal fluid that probably leached calcareous wall rock during ascent.     

Mass Transfer, Oxygen Isotopic Variation and Gold Precipitation in Epithermal System: A Case Study of the Hishikari Deposit, Southern Kyushu, Japan

Abstract: Transportation of various kinds of elements occurred in wall rocks (Quaternary andesites) during the hydrothermal alteration accompanied by the Hishikari epithermal gold mineralization. For example, K₂O and MgO contents of wall rocks decrease away from the gold-quartz veins, while (CaO+Na₂O) content increases, and SiO₂ content is variable near the veins. Hydrothermal alteration zoning and bulk compositional variations in wall rocks suggest that the mixing of hydrothermal solution and acidic groundwater took place an important role as the cause for the hydrothermal alteration and bulk compositional variations. The relationship between dissolved silica concentration and temperature of hydrothermal solution mixed with groundwater is obtained based on precipitation kinetics-fluid flow–mixing model, and the computed results are compared with the distribution of SiO₂ minerals (quartz and cristobalite) in the hydrothermal alteration zones. This comparison suggests that the most reasonable flow rate of fluids migrating through hydrothermal alteration zones, and A/M (A: surface area of rocks interacting with fluid, M: mass of fluid) are estimated to be ca. 10^-4.2 m/sec, and ca. 0.10 m²/kg, respectively. The mixing of two fluids (hydrothermal solution and acidic groundwater) can also explain δ¹⁸O zoning in the altered country rocks, hydrothermal alteration zoning from K-feldspar through K-mica to kaolinite from the center (veins) to margin, and deposition of gold.     

西南天山中新生代盆地成矿流体运移规律

乌拉根铅锌矿床和萨热克铜矿床是西南天山中新生代盆地最有代表性的两个层控砂砾岩型矿床,乌拉根铅锌矿床产于下白垩统克孜勒苏群第五岩性段(K1 kz5)的粗砂质细砾岩中,后期经历了弱的构造改造作用;萨热克铜矿床产于上侏罗统库孜贡苏组上段(J3 k2)杂砾岩中,其北矿段后期经历了强烈的构造改造作用,南矿段可见岩浆热液蚀变作用后...     

Fluid fluxes during low-temperature alteration: implications of multi-style alteration assemblages from the Welsh Borderland,UK

Localized (domainal) low-temperature alteration may indicate variations in the chemistry of alteration fluids and/or discrete fluid flow paths during metamorphism. Occurrences of epidote- and pumpellyite-dominated domains are often used as evidence for large fluxes of Ca-rich fluids. However, comparative studies of two domainal alteration styles from basaltic to andesitic lavas and volcaniclastic rocks at Builth Wells, Wales, UK suggest that such interpretations cannot be applied universally. Here, only one set of domains can be attributed to large fluxes of Ca-rich fluids. In contrast, the second set of domains formed where the host rock supplied the necessary Ca, and fluid/rock ratios were relatively low. These domains are hosted by rocks which show a Caledonian regional metamorphic imprint, characterized by the alteration assemblage albite+chlorite+titanite±prehnite±pumpellyite±calcite±muscovite±quartz (considered to have formed at c. 200°C and ≤2.5 kbar). Type 1 domains lie along fluid channelways, such as veins. Pumpellyite is the dominant secondary mineral, but the alteration assemblage is variable with pumpellyite±prehnite±calcite±titanite±chlorite (±quartz). The domains formed at temperatures of 130–230°C during Ordovician hydrothermal activity, before the peak of regional metamorphism. In contrast, Type 2 domains are not associated with obvious fluid channelways. A central prehnite-dominated zone typically has a rim with the assemblage pumpellyite+calcite±prehnite±chlorite±titanite±K-rich phyllosilicate. These domains probably formed from pelitic xenoliths which contained a volcaniclastic component at temperatures of 130–230°C and at relatively low fluid/rock ratios. However, the timing of domain formation is uncertain. Pyrobitumen, in veins and disseminated throughout the rock, may have influenced the formation of both types of domain by stabilizing pumpellyite in preference to epidote and causing metamorphic calcite formation through the release of CO₂ to the alteration fluids. © 1996 John Wiley & Sons, Ltd.     

Origin of Ore-forming Fluids Responsible for Gold Mineralization of the Pongkor Au-Ag Deposit, West Java, Indonesia: Evidence from Mineralogic, Fluid Inclusion Microthermometry and Stable Isotope Study of the Ciurug–Cikoret Veins

The Pongkor gold–silver mine is situated at the northeastern flank of the Bayah dome, which is a product of volcanism in the Sunda–Banda Arc. The hydrothermal alteration minerals in the Ciurug–Cikoret area are typical of those formed from acid to near‐neutral pH thermal waters. On the surface, illite/smectite mixed layer mineral (I/Sm), smectite and kaolinite, and spotting illite, I/Sm and K‐feldspar alteration occur at the top of the mineralized zone. Silicification, K‐feldspar and I/Sm zones are commonly formed in the wall rock, and gradually grade outwards into a propylitic zone. The mineralization of precious metal ore zone is constrained by fluid temperatures between 180 and 220°C, and with low salinity (<0.2 wt% NaCl equivalent) and boiling condition. The minimum depth of vein formation below the paleo‐water table is approximately 90–130 m for the hydrostatic column. Hydrogen and oxygen isotope data for quartz and calcite show relatively homogeneous fluid composition (?53 to ?68‰δD and ?5.7 to +0.3‰δ¹⁸O H₂O). There is no specific trend in the data with respect to the mineralization stages and elevation, which suggests that the ore‐forming fluids did not significantly change spatially during the vein formation. The stable isotope data indicate mixing between the hydrothermal fluids and meteoric water and interaction between the hydrothermal fluids and the host rock.     

Characteristics of rare-earth elements （REE）, strontium and neodymium isotopes in hydrothermal fluorites from the Bailashui tin deposit in the Furong ore field,southern Hunan Province,China

In this paper the authors present the REE concentrations and Sr and Nd isotopic compositions of fluorites from the Bailashui tin deposit of the Furong ore field, southern Hunan Province. The results showed that the total amount of REE in fluorites is usually low, ranging from 0.705 to 8.785 μg/g with the chondrite-normalized REE distribution patterns similar to those of the Qitianling granites in the study area, characterized by LREE-enrichment patterns with pronounced negative Eu anomalies. The fluorites vary in Sr isotopic composition within the range of 0.7083-0.7091, the values are lower than those of the granites and higher than those of the host carbonate rocks in this area. The εNd（t） values of fluorites vary between -9.4 and ＋10.3, revealing that both the crust- and mantle-source materials were involved in the ore-forming hydrothermal fluids. Combined with previous studies on this ore deposit, the Bailashui tin deposit is temporally and spatially closely related with granitic magmatism in this area. The hydrothermal fluorites are the product of fluid/rock interactions between granitic magmatic hydrothermal fluid and marine carbonate rocks. The REE and F in the ore-forming fluid were derived from the granites, whereas Sr in the ore-forming fluid came mainly from the granitic magmatic hydrothermal fluid and marine carbonate rocks, although variations in Sr isotopic composition cannot be explained by a simple mixture of these two end-members. Evidence demonstrated that the ore-forming fluids are of crustal-mantle mixing origin, but that the fluids were probably incompletely homogenized and this may be caused by inhomogeneous mixing of the fluids of different sources.     

Trace element and isotopic fingerprints in HP–LT metamorphic rocks as a result of fluid–rock interactions (Ile de Groix,France)

Whole rock trace element and isotopic compositions of different HP–LT metamorphic rocks of the Ile de Groix were analysed to characterise geochemical fingerprints during subduction and exhumation in a late Palaeozoic HP metamorphic terrain. Massive metabasites of hydrothermally altered enriched mid-ocean ridge basalt (E-MORB) origin are in association with banded metabasic rocks of volcano-sedimentary origin and metapelites. Fluid-rock interactions that likely occurred during seafloor hydrothermal alteration and early subduction metasomatism increased δ¹⁸O values, as well as K₂O, Na₂O, MgO, and LILE contents and decreased CaO contents of metabasites. Most metabasites have retained their early-subduction and pre-HP trace element and isotopic composition, even for rocks metamorphosed to lower eclogite-facies P–T conditions. Micaschists also preserved apparent pelitic protolith trace element values and oxygen isotopic compositions. During retrograde metamorphism related to the exhumation, metabasites were rehydrated by fluids in equilibrium with the host rock compositions, which were likely derived from the basic rocks. This style of fluid–rock interaction formed a greenschist facies mineral assemblage. Metabasites that underwent pervasive alteration by seafloor hydrothermal and metasomatism processes prior to peak metamorphism, show greater effects of retrogression and albitisation, probably because they were richer in H₂O and Na₂O. The variety of metamorphic assemblages on the Ile de Groix is thus directly related to the pre-HP rock composition. The extent of retrogression in the western part of the Ile de Groix primarily reflects stronger metasomatic intensities than in the eastern part.     

电子探针在蚀变矿物晕研究中的应用

本文选择3种成因的微晶岩石,用电子探针直接在光薄片上进行常规全岩成分分析的实验,并将实验结果与化学分析结果作对比,说明用电子探针粗束斑缓慢移动样品和用细束斑面积扫描两种方法,对某些岩石进行化学成分分析的可行性。作者还采用上述方法,对湘西沃溪Au-Sb-W矿床蚀变矿物晕进行矿物—地球化学微剖面研究,揭示了有关热液矿床围岩蚀变作用过程中元素迁移的规律、岩石退色的机理,提供了矿床成因的信息。     

Southern Alps Cu-Au hydrothermal system,Westland, New Zealand

The Southern Alps of New Zealand is an actively rising mountain belt which displays a thermal anomaly adjacent to the Alpine Fault, the Australian-Pacific plate boundary. Extensive fluid movement occurs in this uplift zone, resulting in metallic vein mineralization. Gold mineralization is confined to greenschist facies rocks, while younger veins in amphibolite facies rocks near the Alpine Fault are enriched in copper. Transport and deposition of metals in this complex hydrothermal system is governed by interaction between rising metamorphic fluids and downward-percolating meteoric fluid. Metamorphic fluids have equilibrated with graphitic schist country rock and are relatively reduced. Infiltration and mixing of meteoric water increases oxygen activity and decreases sulphur activity in the fluid. Oxidised meteoric water heats up and dissolves Cu during downward percolation. This Cu is deposited as the fluid becomes more reduced. Hence, there is a progressive increase in copper content in the middle portions of the hydrothermal system, especially in the more permeable highly fractured rocks near the Alpine Fault.     

The magmatic–hydrothermal transition—evidence from quartz phenocryst textures and endoskarn abundance in Cu–Zn skarns at the Empire Mine, Idaho, USA

Information about the magmatic to hydrothermal transition is preserved in late-stage features of quartz phenocrysts and endoskarn alteration in some Cu–Zn skarn deposits such as the Empire Mine in Idaho. Important features include: (1) quartz phenocrysts with strong resorption textures such as vermicular zones of igneous groundmass cutting primary quartz cathodoluminescence banding, (2) anomalous amounts of endoskarn (more than 50% of mineralized rock), (3) high F activities as evidenced by fluorite as an accessory mineral in igneous rocks, in alteration assemblages, and in fluid inclusions and by high F in hydroxyl sites in igneous biotite and amphibole, and (4) direct association of Zn, which normally is deposited distally at low temperature, with Cu in proximal locations and in endoskarn. These features are explained by the following model: (1) F lowers the solidus temperature of the magma, thus changing the timing, temperature, and duration of hydrothermal fluid exsolution. (2) Upon magmatic vapor saturation the F-rich hydrothermal fluids form bubbles that adhere to quartz phenocrysts and chemically corrode/tunnel into the quartz forming vermicular resorption textures. (3) F-rich hydrothermal fluids also promote the formation of endoskarn; silicic rocks are attacked by F-rich fluids in the same sense that carbonate wall rocks are dissolved by weakly to moderately acidic hydrothermal fluids. (4) Low fluid exsolution temperature facilitated by high F activity promotes high Zn/Cu ratios in proximal locations due to the solubility of Zn relative to Cu at lower temperatures. This model may be applicable at other localities such as the world-class Cu–Zn skarn Antamina mine, as well as some tin and rapakivi granites.