Genesis of the Jinding Zn-Pb deposit,northwest Yunnan Province,China: Constraints from rare earth elements and noble gas isotopes

The giant sediment-hosted Jinding zinc-lead deposit is located in the Lanping Basin, northwestern Yunnan Province, China. The genesis of the deposit has long been debated and the sources of the ore-forming fluids and metals are controversial. This study presents rare earth element (REE) and noble gas isotope data that constrain the origins of the ore fluids and the heat source driving the hydrothermal circulation. The early-stage sulfides are enriched in light REEs and have high ∑REE values (30.8–94.8 ppm) and weakly negative Eu (δEu 0.85–0.89) and Ce anomalies (δCe 0.84–0.95), suggesting that the fluids were likely derived from dissolution of Upper Triassic marine carbonates with input of REEs from aluminosilicate rocks in the basin. In contrast, the late-stage sulfides have irregular REE patterns, generally low ∑REE values (0.24–10.8 ppm) and positive Eu (δEu 1.22–10.9) and weakly negative Ce anomalies (δCe 0.53–0.90), which suggest that the ore-forming fluids interacted with evaporite minerals. The ³He/⁴He (0.01–0.04 R_a) and ⁴⁰Ar/³⁶Ar values (301–340) of the ore-forming fluids indicate crustal and atmospheric origins for these noble gases. These findings are in agreement with the published fluid inclusion microthermometry data and the results of H, O, C, S, Pb and Sr isotope studies. Our data, in combination with published results, support a two-stage hydrothermal mineralization model, involving early-stage basinal brines and late-stage meteoric water that acquired metals and heat from crustal sources.     

塔里木盆地下奥陶统白云岩化流体来源的地球化学分析

塔里木盆地是中国重要的含油气盆地,其中奥陶系白云岩是主要储层之一,然而有关白云岩成因的问题众说纷纭,其中的关键是对于白云岩化流体性质的认识不一。元素地球化学和同位素测试分析表明,白云岩的稀土元素来源大部分继承原始灰岩,具有与海水类似的配分特征,只不过稀土元素的含量明显增高了;Sr、Ti含量和Sr/Ba比值较高,且Sr和Mn都具典型的埋藏演化特征;碳、氧同位素分布于正常海相范围内,与典型的埋藏白云岩特征类似;在局部发育一些与断裂相关的铁(锰)白云岩和鞍状白云岩,显示明显的Eu正异常,具相对较高的Fe-Mn-Ba-Si(-Zn-Pb)元素含量及Sr/Ba比值。分析结果说明塔中和塔北下奥陶统的白云岩化流体主要为正常或浓缩了的海水,白云岩形成于准同生和/或埋藏环境,局部发育与断裂相关的热液白云岩,而前人强调的大气淡水或混合水作用对白云岩的形成并不重要。     

Geochemistry of Platinum Group and Rare Earth Elements of the Polymetallic Layer in the Lower Cambrian, Weng’an, Guizhou Province

Abstract: The black shales of the Lower Cambrian Niutitang Formation in Weng’an, on the Yangtze platform of south China, contain voluminous polymetallic sulfide deposits. A comprehensive geochemical investigation of trace, rare earth, and platinum group elements (PGE) has been undertaken in order to discuss its ore genesis and correlation with the tectono-depositional setting. The ore-bearing layers enrich molybdenum (Mo), nickel (Ni), vanadium (V), lead (Pb), strontium (Sr), barium (Ba) , uranium (U) , arsenic (As), and rare earth elements (REE) in abundance. High uranium/thorium (U/Th) ratios (U/Th>1) indicated that mineralization was mainly influenced by the hydrothermal process. The dU value was above 1.9, showing a reducing sedimentary condition. The REE patterns showed high enrichment in light rare earth elements (LREE) (heavy rare earth elements (HREE) (LREE/HREE=5–17), slightly negative europium (Eu) and cerium (Ce) anomalies (dEu=0.81–0.93), and positive Ce anomalies (dCe=0.76–1.12). PGE abundance was characterized by the PGE-type distribution patterns, enriching platinum (Pt), palladium (Pd), ruthenium (Ru) and osmium (Os). The Pt/Pd ratio was 0.8, which is close to the ratios of seawater and ultramafic rocks. All of these geochemical features suggest that the mineralization was triggered by hydrothermal activity in an extensional setting in the context of break-up of the Rodinian supercontinent.     

Trace element and REE geochemistry of Sanshenjiang gold deposit, southeastern Guizhou Province, China

The Sanshenjiang gold deposit in southeastern Guizhou Province, China, is hosted by the Neoproterozoic metasedimentary rocks which experienced low-grade greenschist facies metamorphism. Gold mineralization occurs mainly in the ribbon chiltern slate of the first member of the Longli Formation and is controlled by both strata and faults. Ore bodies are characterized by abundant quartz-arsenopyrite-gold-pyrite-bedding veins, veinlets and small lenses within the shear zone. In this study, trace element and REE geochemistry was analyzed to constrain the origin and genesis of this deposit. The trace element signatures of wall rocks and veins display a basically similar tendency in the spider diagram, showing the genetic relationship. The values of Co/Ni, Y/Ho, Hf/Sm, Nb/La and Th/La reflect that the hydrothermal fluids of this deposit were derived from the mixture of multiple sources with marked enrichment of Cl and moderate to high temperature. There is a broad similarity in the chondrite-normalized patterns and REE fractionation between wall rocks and ore bodies, possibly reflecting their similar origin. Based on the difference in δCe and δEu, quartz veins and lenses can be subdivided into weakly negative Ce-anomalies (δCe=0.81 to 1.06) with slight Eu anomalies (δEu=0.81 to 1.06) type and the significant positive Ce-anomalies (δCe=1.13 to 1.97) with moderate negative Eu-anomalies type, probably suggesting physical-chemical changes in the evolution process of ore-forming fluids from the early to late stage. It can be concluded that the ore-forming process may have experienced three stages: formation of the original ore source bed, regional metamorphism and gold mineralization, on the basis of trace element and REE analysis and field observation.     

Rare earth element and strontium isotope geochemistry in Dujiali Lake,central Qinghai-Tibet Plateau,China: Implications for the origin of hydromagnesite deposits

Rare earth element (REE) and strontium isotope data (⁸⁷Sr/⁸⁶Sr) are presented for hydromagnesite and surface waters that were collected from Dujiali Lake in central Qinghai-Tibet Plateau (QTP), China. The goal of this study is to constrain the solute sources of hydromagnesite deposits in Dujiali Lake. All lake waters from the area exhibit a slight LREE enrichment (average [La/Sm]_PAAS = 1.36), clear Eu anomalies (average [Eu/Eu*]_PAAS = 1.31), and nearly no Ce anomalies. The recharge waters show a flat pattern (average [La/Sm]_PAAS = 1.007), clear Eu anomalies (average [Eu/Eu*] _PAAS = 1.83), and nearly no Ce anomalies (average [Ce/Ce*]_PAAS = 1.016). The REE+Y data of the surface waters indicate the dissolution of ultramafic rock at depth and change in the hydrogeochemical characteristics through fluid-rock interaction. These data also indicate a significant contribution of paleo-groundwater to the formation of hydromagnesite, which most likely acquired REE and Sr signatures from the interaction with ultramafic rocks. The ⁸⁷Sr/⁸⁶Sr data provide additional insight into the geochemical evolution of waters of the Dujiali Lake indicating that the source of Sr in the hydromagnesite does not directly derive from surface water and may have been influenced by both Mg-rich hydrothermal fluids and meteoric water. Additionally, speciation modeling predicts that carbonate complexes are the most abundant dissolved REE species in surface water. This study provides new insights into the origins of hydromagnesite deposits in Dujiali Lake, and contributes to the understanding of hydromagnesite formation in similar modern and ancient environments on Earth.     

Seawater contribution to polymetallic Ni–Mo–PGE–Au mineralization in Early Cambrian black shales of South China: Evidence from Mo isotope,PGE, trace element,and REE geochemistry

The Early Cambrian black shale sequence of the Niutitang Formation in South China hosts a synsedimentary, organic carbon-rich, polymetallic sulfide layer with extreme metal concentrations, locally mined as polymetallic Ni–Mo–PGE–Au ore. In combination with previously reported data, we present Mo isotope, platinum-group element (PGE), and trace and rare-earth element (REE) data for the polymetallic sulfide ores and host black shales from four mine sites (Dazhuliushui and Maluhe in Guizhou Province, and Sancha and Cili in Hunan Province, respectively), several hundred kilometers apart. The polymetallic sulfide ores have consistently heavy δ^98/95Mo values of 0.94 to 1.38‰ (avg. 1.13 ± 0.14‰, 1σ, n = 11), and the host black shale and phosphorite have slightly more variable δ^98/95Mo values of 0.81‰ to 1.70‰ (n = 14). This latter variation is due to variable paleoenvironmental conditions from suboxic to euxinic, and partly closed-system fractionation in isolated marine sedimentary basins. Both the polymetallic sulfides and host black shales show PGE distribution patterns similar to that of present-day seawater, but different from those of ancient submarine-hydrothermal deposits and modern submarine hydrothermal fluids. The polymetallic sulfide bed has a generally consistent metal enrichment by a factor of 10⁷ compared to present-day seawater. PAAS-normalized REE + Y patterns of the polymetallic sulfide bed are characterized by a remarkably positive Y anomaly, consistent with an origin of the REE predominantly from seawater. Small positive Eu anomalies in some of the sulfide ores could reflect minor hydrothermal components involved. The Mo isotope, PGE, and trace and rare-earth element geochemical data suggest that metals in the polymetallic Ni–Mo–PGE–Au sulfide ore layer were scavenged mostly from Early Cambrian seawater, by both in-situ precipitation and local re-deposition of sulfide clasts.     

The vein-type barite mineralization of the Draïssa ore field,Ougarta; SW- Algeria: mineralogy,trace elements and halogens

The Draïssa barite vein system in the Ougarta district is located in southwestern Algeria. It is the principal mineral deposit of economic interest of the area. The mineralization is hosted by Cambrian sedimentary rocks that unconformably overlie Precambrian formations. The mineralized structures consist mostly of barite and quartz with minor sulfide minerals and trend dominantly NE-SW, NW-SE, and E-W. Siliceous alteration zones are associated with the vein system. Samples of barite ore are characterized by low total REE contents ranging from 9 to 50 ppm and positive Eu (2–2.15 ppm) and Y (1.2–11.1 ppm) anomalies, indicating hydrothermal activity during mineralization. Halogen data of the barite show that the Cl/Br molar ratio is 189:571 and the Na/Br ratio is 34:376, indicating that the sulfur was derived from seawater. The Ba-enrichment trend in the volcanic rocks of Draïssa is interpreted as possible probable source of the Ba (424–3039 ppm Ba). It appears that the barite-quartz deposits were formed in two stages. Endogenous fluids deposited the primary vein materials, consisting of quartz associated with copper sulfides. Exogenous fluids (cold seawater) became heated during ascendant fluid movement. Mineralization was governed by convective motions and the barite and galena fillings were deposited in openings created by normal faulting.     

Geochemical constraints on the modes of carbonate precipitation in peridotites from the Logatchev Hydrothermal Vent Field and Gakkel Ridge

The ultramafic-hosted Logatchev Hydrothermal Field (LHF) at 15°N on the Mid-Atlantic Ridge and the Arctic Gakkel Ridge (GR) feature carbonate precipitates (aragonite, calcite, and dolomite) in voids and fractures within different types of host rocks. We present chemical and Sr isotopic compositions of these different carbonates to examine the conditions that led to their formation. Our data reveal that different processes have led to the precipitation of carbonates in the various settings. Seawater-like ⁸⁷Sr/⁸⁶Sr ratios for aragonite in serpentinites (0.70909 to 0.70917) from the LHF are similar to those of aragonite from the GR (0.70912 to 0.70917) and indicate aragonite precipitation from seawater at ambient conditions at both sites. Aragonite veins in sulfide breccias from LHF also have seawater-like Sr isotope compositions (0.70909 to 0.70915), however, their rare earth element (REE) patterns show a clear positive europium (Eu) anomaly indicative of a small (< 1%) hydrothermal contribution. In contrast to aragonite, dolomite from the LHF has precipitated at much higher temperatures (~ 100 °C), and yet its ⁸⁷Sr/⁸⁶Sr ratios (0.70896 to 0.70907) are only slightly lower than those of aragonite. Even higher temperatures are calculated for the precipitation of deformed calcite veins in serpentine–talc fault schists form north of the LHF. These calcites show unradiogenic ⁸⁷Sr/⁸⁶Sr ratios (0.70460 to 0.70499) indicative of precipitation from evolved hydrothermal fluids. A simple mixing model based on Sr mass balance and enthalpy conservation indicates strongly variable conditions of fluid mixing and heat transfers involved in carbonate formation. Dolomite precipitated from a mixture of 97% seawater and 3% hydrothermal fluid that should have had a temperature of approximately 14 °C assuming that no heat was transferred. The much higher apparent precipitation temperatures based on oxygen isotopes (~ 100 °C) may be indicative of conductive heating, probably of seawater prior to mixing. The hydrothermal calcite in the fault schist has precipitated from a mixture of 67% hydrothermal fluid and 33% seawater, which should have had an isenthalpic mixing temperature of ~ 250 °C. The significantly lower temperatures calculated from oxygen isotopes are likely due to conductive cooling of hydrothermal fluid discharging along faults. Rare earth element patterns corroborate the results of the mixing model, since the hydrothermal calcite, which formed from waters with the greatest hydrothermal contribution, has REE patterns that closely resemble those of vent fluids from the LHF. Our results demonstrate, for the first time, that (1) precipitation from pure seawater, (2) conductive heating of seawater, and (3) conductive cooling of hydrothermal fluids in the sub-seafloor all can lead to carbonate precipitation within a single ultramafic-hosted hydrothermal system.     

Petrogenesis of Ore‐Related Granodiorite Porphyry in the Jiande Copper Deposit,SE China: Implications for the Tectonic Setting and Mineralization

Adakitic rocks and related Cu–Au mineralization are widespread along eastern Jiangnan Orogen in South China. Previous studies have mainly concentrated on those in the Dexing area in northeastern Jiangxi Province, but information is lacking on the genesis and setting of those in northwestern Zhejiang Province. The Jiande copper deposit is located in the suture zone between the Yangtze and Cathaysia blocks of South China. This paper presents systematic LA–ICP–MS zircon U–Pb dating and element and Sr–Nd–Hf isotopic data of the Jiande granodiorite porphyry. Zircon dating showed that the Jiande granodiorite porphyry was produced during the Middle Jurassic (ca. 161 Ma). The Jiande granodiorite porphyry is characterized by adakitic geochemical affinities with high Sr/Y and La_N/Yb_N ratios but low Y and Yb contents. The absence of a negative Eu anomaly, extreme depletion in Y and Yb, relatively low MgO contents, and relatively high ²⁰⁷Pb/²⁰⁴Pb ratios, indicated that the Jiande granodiorite porphyry was likely derived from partial melting of the thickened lower continental crust. In addition, the Jiande granodiorite porphyry shows arc magma geochemical features (e.g., Nb, Ta and Ti depletion), with bulk Earth‐like ε_Nd (t) values (?2.89 to ?1.92), ε_Hf (t) values (?0.6 to +2.8), and initial ⁸⁷Sr/⁸⁶Sr (0.7078 to 0.7105). However, a non‐arc setting in the Middle Jurassic is indicated by the absence of arc rocks and the presence of rifting‐related igneous rock associations in the interior of South China. Combined with the regional Neoproterozoic Jiangnan Orogeny, it indicates that these arc magma geochemical features are possibly inherited from the Neoproterozoic juvenile continental crust formed by the ancient oceanic crust subduction along the Jiangnan Orogen. The geodynamic environment that is responsible for the development of the Middle Jurassic Jiande granodiorite porphyry is likely a localized intra‐continental extensional environment along the NE‐trending Jiangshan‐Shaoxing Deep Fault as a tectonic response to far‐field stress at the margins of the rigid South China Plate during the early stage of the paleo‐Pacific plate subduction. In terms of Cu mineralization, we suggest that the metal Cu was released from the subducted oceanic slab and reserved in the juvenile crust during Neoproterozoic subduction along the eastern Jiangnan Orogen region. Partial melting of the Cu rich Neoproterozoic juvenile crust during the Middle Jurassic time in the Jiande area caused the formation of adakitic rocks and the Cu deposit.     

贵州渣拉沟剖面下寒武统黑色硅质岩微量元素富集机制

华南早寒武世发育了一套富有机质黑色硅质岩,其成因尚有较大争议。选择贵州省三都县渣拉沟剖面早寒武世牛蹄塘组底部硅质岩段进行研究,发现该硅质岩具有微量元素富集的特征。其可能的原因包括,静海环境、上升流和热液活动。Ce/Ce*比值显示硅质岩沉积时水体为次氧化条件,不支持静海环境;而Ba、Zn、Cu、Ni、Cd、P与有机碳含量不存在相关关系,也不支持上升流为微量元素富集的主要原因。Al-Fe-Mn三角图、Al2O3/(Fe2O3+Al2O3)、REY配分模式等指标则表明存在热液活动。上述认识与现代上升流、静海环境的微量元素富集系数对比结果相吻合。与华南地区早寒武世初期不同沉积环境硅质岩对比,发现:深海环境并不富集Ba、Zn、Cu、Ni等氧化还原敏感元素,而沿着斜坡相带同沉积断层分布的热液活动,更有可能造成这些微量元素的富集。     

Tracing element sources of hydrothermal mineral deposits: REE and Y distribution and Sr-Nd-Pb isotopes in fluorite from MVT deposits in the Pennine Orefield,England

Fluorite from Mississippi Valley Type (MVT) deposits in the South Pennine Orefield, England, displays significantly different distributions of rare earths and yttrium (REY) compared to fluorite from similar MVT deposits in the North Pennine Orefield. Samples from the South Pennine Orefield display negative Ce and positive Gd and Y anomalies but lack any Eu anomaly, indicating that the REY were mobilized from relatively pure marine sedimentary carbonates. In marked contrast, fluorite from the North Pennine Orefield lacks any Ce and Gd anomalies but shows a pronounced positive Eu anomaly, suggesting that the REY were provided by different source rock(s), that the mineralizing hydrothermal fluid had experienced higher temperatures prior to fluorite precipitation, and that it was derived from deeper crustal levels in the north compared to the south. The isotopic composition of Sr in Blue John fluorite from the South Pennine Orefield suggests that Sr was mobilized from Lower Carboniferous (Tournaisian) limestones, whereas Pb isotopes suggest that in contrast to REY and Sr, Pb was derived from aluminosilicate rocks. Neither Nd nor Sr or Pb isotopes can be used to radiometrically date the formation of Blue John fluorite. All isotope systems studied indicate that the limestone host rock of this fluorite mineralization did not contribute to the trace element budget of the hydrothermal fluid. Our results show that different solutes in a natural water (hydrothermal fluid, groundwater, etc.) may be derived from different sources, and that the study of a small set of elements or isotope ratios may not provide full insight into the genesis or history of a mineralization or a hydrothermal fluid. Our data provide evidence for the uncoupling of Sr, Nd and Pb during fluid-rock interaction and fluid migration, and show that the use of plots such as ⁸⁷Sr/⁸⁶Sr vs. _Nd. to learn about mixing relationships (as is commonly done in igneous geochemistry) is unreliable when applied to natural waters and their precipitates.Editorial handling: B. Lehmann     

Formation and age of sphalerite mineralization in carbonate rocks of Bajocian age in the Swiss Jura Mountains: evidence of Mesozoic hydrothermal activity

A combination of petrographic and geochemical techniques was applied to better constrain the origin and evolution of the fluid systems responsible for the formation of disseminated, Cd-rich (up to 0.6 wt%), sphalerite (ZnS) mineralization in the northeastern part of the Jura Mountains, Switzerland. The Rb–Sr ages of sphalerite samples indicate that a main phase of sphalerite formation occurred near the boundary between the late Middle and early Late Jurassic, at around 162 Ma. The negative δ³⁴S values (?22.3 to ?5.3 ‰) suggest that biogenic sulfide sulfur was involved in ZnS precipitation. The strontium isotope composition is more radiogenic than that of contemporaneous seawater, reflecting the interaction of mineralizing fluids with silicate rocks. Lead isotope signatures are very uniform (²⁰⁶Pb^/204Pb = 18.63–18.67, ²⁰⁷Pb^/204Pb = 15.63–15.64, ²⁰⁸Pb^/204Pb = 38.51–38.63), indicating an isotopically well-homogenized fluid system. The basement rocks underlying the Jurassic strata are considered to be the main source of metals for the sphalerite mineralization. The migration of deep-sourced hydrothermal saline metal-bearing fluids into the Bajocian host carbonates containing sedimentary reduced sulfur resulted in the precipitation of sulfides. The period of sphalerite formation near the Middle–Late Jurassic boundary is characterized by enhanced tectonic and hydrothermal activity in Europe, related to the opening of the Central Atlantic and tectonic/thermal subsidence during spreading of the Alpine Tethys. Our study provides evidence that the Bajocian carbonate rocks in the Jura Mountains area were affected by the circulation of deep-sourced metal-bearing hydrothermal fluids in response to these continent-wide tectonothermal events. The presence of sphalerite mineralization and associated geochemical anomalies in Zn and Cd contents in carbonate rocks may also be used to trace basement features.     

铀的地球化学性质与成矿——以华南铀成矿省为例

铀是强不相容元素,随着岩浆演化而不断富集,在岩浆演化末期受结构氧增加影响进入独居石、磷钇矿等副矿物中。岩浆演化通常无法直接形成达到工业品位的铀矿床。铀是对氧逸度敏感的变价元素。在表生风化过程中岩体(层)中的铀被氧化为UO_2~(2+)而极易溶解进入水体中,并可在还原环境沉淀而富集成矿,氧化还原界面是找矿的理想选区。大气水可通过断裂构造系统进入一定深度,并受热源作用形成高氧逸度的热液而萃取出岩体(层)中的铀在还原位置沉淀富集形成矿床。新元古代氧化事件以及Marinoan冰期结束使得表生风化过程中更多的U进入水体;而寒武纪生命大爆发,易在沉积盆地底部形成还原环境,有利于U的沉淀富集。受上述三方面因素控制,在华南形成了广泛分布的富铀黑色页岩层,并被之后的沉积物覆盖,成为华南各型铀矿床的铀源层。印支期构造运动使部分富铀黑色页岩层发生部分熔融形成了富铀的S型花岗岩,该类岩石亦是之后铀成矿作用的铀源岩。燕山运动后期华南发生伸展构造背景下的岩浆热事件为以大气水为主的高氧逸度热液的形成并作用于铀源岩(层)提供了有利条件,促使华南各类型铀矿床开始在白垩纪集中形成。     

Trace-element and Sr–Nd isotopic evidence for the origin of the Sardinian fluorite mineralization (Italy)

The fluorite-bearing hydrothermal mineralization in Sardinia mainly occurs within Paleozoic volcanic and metasedimentary rocks. Only 3 occurrences are located in volcanic and siliciclastic Cenozoic rocks. Most Sardinian fluorites exhibit relatively high rare earth and Y (REY) contents, strong positive Y anomalies, slightly negative Ce and generally positive Eu anomalies. These features indicate that the REY were mobilized mainly from non-carbonate rocks. Neither Sr nor Nd isotopes can be used to date radiometrically the Sardinian fluorites. However, the measured Sr-isotope ratios of the fluorites hosted by Paleozoic rocks fit mixing lines in the 1000/Sr versus ⁸⁷Sr/⁸⁶Sr plot once recalculated at 280 Ma, suggesting that the age inferred for the correction probably represents that of the formation of the fluorite mineralization. Mixing likely occurred between diluted surficial waters and brines circulating mainly through the Lower Paleozoic metasedimentary basement. The Cenozoic fluorites exhibit chemical and isotopic features similar to those of the Paleozoic fluorites, except the Nuraghe Onigu fluorite displaying a possible contribution of Sr from Cenozoic magmatic rocks. The initial ε_Nd values of the Paleozoic fluorites fit the age proposed for the formation of the deposits. Moreover, the values suggest that radiogenic Nd was provided to the fluids from the Ordovician siliciclastic basement, except for 3 deposits where the potential source rocks of Nd were mainly Ordovician acidic magmatic rocks. The initial ε_Nd values of the Cenozoic fluorites suggest a provenance of Nd essentially from the leaching of Variscan granitoids.     

长坑矿田金,银矿床地球化学特征及形成差异分析

长坑矿田金、银矿体主要产于下石炭统与上三叠统不整合面之下的硅质岩中,金、银矿体分离。金矿体主要为浸染状,富集As、Sb、Hg;银矿体主要为脉状,富集Cu、Pb、Zn。金矿体铅同位素组成与寒武纪—石炭纪地层及硅质岩的相同,银矿体铅同位素组成与金矿体的不同。金、银矿体的氢、氧、碳同位素组成也明显不同。银矿体Rb-Sr等时线年龄为70.4Ma。据上述特征,笔者认为长坑金、银矿床是不同成矿作用形成的,金矿主要是热水沉积形成,银矿主要是燕山期晚期改造形成。     

The composition of garnet in garnet-rich rocks in the southern Proterozoic Curnamona Province, Australia: an indicator of the premetamorphic physicochemical conditions of formation

Garnet-rich rocks occur throughout the Proterozoic southern Curnamona Province, Australia, where they are, in places, spatially related to Broken Hill-type Pb-Zn-Ag deposits. Fine-scale bedding in these rocks, their conformable relationship with enclosing metasedimentary rocks, and their enrichment in Mn and Fe suggest that they are metamorphosed chemical precipitates. They formed on the floor of a 1.69?Ga continental rift basin from hydrothermal fluids mixed with seawater and detritus. Garnet in garnet-quartz and garnet-amphibole rocks is generally light rare earth element (LREE) depleted, and has flat heavy REE (HREE) enriched chondrite-normalized REE patterns, and negative Eu anomalies (Eu/Eu*?<?1). Garnet in garnet-rich rocks from the giant Broken Hill deposit has similar REE patterns and either positive (Eu/Eu*?>?1) or negative Eu anomalies. Manganese- and Mn-Ca-rich, Fe-poor garnets in garnetite, garnet-hedenbergite, and garnet-cummingtonite rocks at Broken Hill have Eu/Eu*?>?1, whereas garnet in Mn-poor, Fe-rich quartz garnetite and quartz-garnet-gahnite rocks from Broken Hill, and quartz garnetite from other locations have Eu/Eu*?<?1. The REE patterns of garnet and its host rock and interelement correlations among REEs and major element contents in garnet and its host rock indicate that the Eu anomaly in garnet reflects that of its host rock and is related to the major element composition of garnet and its host rock. The value of Eu/Eu* in garnet is related to its Mn, Fe, and Ca content and that of its host rock, and the distribution of REEs among garnet and accessory phases (e.g., feldspar). Positive Eu anomalies reflect high amounts of Eu that was preferentially incorporated into Mn- and Mn-Ca-rich oxides and carbonates in the protolith. In contrast, Eu/Eu*?<?1 indicates the preferential discrimination against Eu by Fe-rich, Mn-poor precursor minerals. Precursors to Mn-rich garnets at Broken Hill formed by precipitation from cooler and more oxidized hydrothermal fluids compared to those that formed precursors to Mn-poor, Fe-rich garnet at Broken Hill and the other locations. Garnet from the Broken Hill deposit is enriched in Zn (> 400?ppm), Cr (> 140?ppm), and Eu (up to 6?ppm and positive Eu anomalies), and depleted in Co, Ti, and Y compared to garnet in garnet-rich rocks from other localities. These values, as well as MnO contents ?>?15 wt. % and Eu/Eu*?>?1 are only found at the Broken Hill deposit and are good indicators of the presence of Broken Hill-type mineralization.     

Hydrothermal Dolomite in the Upper Sinian (Upper Proterozoic) Dengying Formation,East Sichuan Basin,China

Hydrothermal Dolomite （HTD） is present in the Upper Sinian （Upper Proterozoic） Dengying Formation, east Sichuan Basin, China. The strata are comprised by primary dolomite. The HTD has various textures, including zebra dolomite, subhorizontal sheet-like cavities filled by saddle dolomite and breccias cemented by saddle dolomites as well occur as a fill of veins and fractures. Also co-occur MVT type lead-zinc ores in the study area. The δ13C and δ18O isotopes of HTD in the Upper Sinian Dengying Formation are lighter than those of the host rocks, while STSr/86Sr is higher. The apparent difference in carbon, oxygen and strontium isotopes, especially the large difference in S7Sr/S6Sr isotopes ratio indicate crystallization from hot basinal and/or hydrothermal fluids. Saddle dolomite was precipitated at temperatures of 270-320℃. The diagenetic parasequences of mineral assemblage deposited in the Dengying Formation are： （1） dolomite host rock →sphalerite-galena-barite-fluorite; （2） dolomite host rock →saddle dolomite →quartz; （3） dolomite host rock →saddle dolomite→bitumen; （4） dolomite host rock →saddle dolomite →barite. The mean chemical composition of the host dolomite matrix and HTD didn＇t change much during hydrothermal process. The fluids forming the HTDs in the Dengying Formation were mixtures of freshwater from the unconformity at the top of Sinian, fluids from diagenetic compaction and hydrocarbon generation ＆ expulsion from the Lower Cambrian Niutitang Formation mudstones or the Doushantuo Formation silty mudstones, and hydrothermal fluids from the basement. The hydrocarbon reservoirs associated with the HTD were mostly controlled by the basement faults and fractures and karsting processes at the unconformity separating Sinian and Cambrian strata. The hydrocarbon storage spaces of HTD included dissolved cavities and intercrystalline pores. Dissolution cavities are extensive at the top of Dengying Formation, up to about 46m below the unconformity between Sinian an     

Fe Isotope Compositions of Cyprus Umbers

Submarine metalliferous sedimentary rocks are chemical precipitates resulted from hydrothermal exhalation near mid‐ocean ridge or faults. They record the submarine hydrothermal activity between lithosphere and hydrosphere and are critical for understanding Fe cycling in marine environment. Fe was expelled from the hydrothermal vent systems and was oxidized and precipitated in the ambient seawater, where the precipitation of hydrothermal Fe is largely controlled by oxidation state of seawater and is potentially revealed by its Fe isotope compositions. This hydrothermal process in modern hydrothermal vent systems have been well observed, but that for the ancient ones are still not well known. Umbers, or ferromanganoan sediments, overlying Troodos ophiolite in Cyprus of Mid‐Cretaceous age thus provides an excellent example for understanding the Fe cycles in ancient submarine hydrothermal process. Samples were collected from Margi village in Troodos and are mostly amorphous Fe‐Mn oxy‐hydroxides with very minor quartz, goethite, smectite and silicates such as clinopyroxene derived from the volcanic rocks. There is no terrestrial, detrital component. Samples were analyzed for their whole‐rock element and Fe isotope compositions. The results show that samples are composed mainly of SiO₂ (13～80 wt%), Fe₂O₃ (9～54 wt%) and MnO (1.5～10.4 wt%), with minor Al₂O₃ (0.7～4.3 wt%). PAAS‐normalized REE patterns are near flat with significantly negative Ce anomalies (Ce/Ce* is from 0.2 to 0.5) and slightly positive Eu anomalies (Eu/Eu* is around 1.1), indicating a source from the oxidized seawater and the high‐temperature hydrothermal fluids. δ⁵⁶FeIRMM‐014 values of samples are ‐0.32‰ to ‐0.15‰, with an average of ‐0.20‰, which are consistent with those of the hydrothermal fluids previously reported. The narrow Fe isotope compositions of Cyprus umbers that are close to those of submarine hydrothermal fluids indicates near complete oxidation of hydrothermal Fe²⁺ during its expulsion from the hydrothermal vent.     

Evaluating new fault-controlled hydrothermal dolomitization models: Insights from the Cambrian Dolomite,Western Canadian Sedimentary Basin

Fault-controlled hydrothermal dolomitization in tectonically complex basins can occur at any depth and from different fluid compositions, including ‘deep-seated’, ‘crustal’ or ‘basinal’ brines. Nevertheless, many studies have failed to identify the actual source of these fluids, resulting in a gap in our knowledge on the likely source of magnesium of hydrothermal dolomitization. With development of new concepts in hydrothermal dolomitization, the study aims in particular to test the hypothesis that dolomitizing fluids were sourced from either seawater, ultramafic carbonation or a mixture between the two by utilizing the Cambrian Mount Whyte Formation as an example. Here, the large-scale dolostone bodies are fabric-destructive with a range of crystal fabrics, including euhedral replacement (RD1) and anhedral replacement (RD2). Since dolomite is cross-cut by low amplitude stylolites, dolomitization is interpreted to have occurred shortly after deposition, at a very shallow depth (<1 km). At this time, there would have been sufficient porosity in the mudstones for extensive dolomitization to occur, and the necessary high heat flows and faulting associated with Cambrian rifting to transfer hot brines into the near surface. While the δ¹⁸O_water and ⁸⁷Sr/⁸⁶Sr ratios values of RD1 are comparable with Cambrian seawater, RD2 shows higher values in both parameters. Therefore, although aspects of the fluid geochemistry are consistent with dolomitization from seawater, very high fluid temperature and salinity could be suggestive of mixing with another, hydrothermal fluid. The very hot temperature, positive Eu anomaly, enriched metal concentrations, and cogenetic relation with quartz could indicate that hot brines were at least partially sourced from ultramafic rocks, potentially as a result of interaction between the underlying Proterozoic serpentinites and CO₂-rich fluids. This study highlights that large-scale hydrothermal dolostone bodies can form at shallow burial depths via mixing during fluid pulses, providing a potential explanation for the mass balance problem often associated with their genesis.     

Role of basement in epithermal deposits: The Kushikino and Hishikari gold deposits,southwestern Japan

The magma–ore deposit relationship of most low-sulfidation epithermal ore deposits is still unclear, partly because many stable isotopic studies of such deposits have indicated the predominance of meteoric waters within hydrothermal fluids. However, it is certainly true that hydrothermal systems are ultimately driven by magmatic intrusions, and epithermal gold deposits might therefore be produced by magmatic activity even in deposits having has no obvious links to a magma. We re-examine the genesis of two typical low-sulfidation epithermal gold deposits, the Kushikino and Hishikari deposits, using structural simulations and isotope data.Many epithermal gold deposits including the Kushikino and Hishikari deposits have been discovered in Kyushu, southwestern Japan. The Kushikino deposit comprises fissure-filling veins within Neogene andesitic volcanics that overlie unconformably Cretaceous sedimentary basement. The veins consist of gold- and silver-bearing quartz and calcite with minor amounts of adularia, sericite and sulfides. Although carbon and oxygen isotopic data for the veins indicate a meteoric origin of the ore fluid, finite element simulations suggest that the vein system might have formed in direct response to magma intrusion. In particular, geophysical data suggest that intruding magma has uplifted the basement rocks, thereby producing fractures and veins and a positive Bouguer anomaly, and providing the heat necessary to drive an ore-forming hydrothermal system.The second component of this study has been to investigate the nature and evolution of the Kushikino and Hishikari epithermal systems. Isotope data document the geochemical evolution of the hydrothermal fluids. We conclude that the existence of sedimentary basement rocks at depth might have affected the strontium and carbon isotopic ratios of the Kushikino and Hishikari ore fluids. The ⁸⁷Sr/⁸⁶Sr ratios and δ¹³C–δ¹⁸O trend reveal that major ore veins in the Hishikari deposit can be distinguished from shallow barren veins. It was suggested isotopically that fluids responsible for the barren veins in nearby shallow and barren circulation systems were only controlled by the shallow host rocks. Such multi-isotope systematics provide a powerful tool with which to determine the center of hydrothermal activity and thereby document the evolution of hydrothermal fluids.