Studies of colloids and suspended particles,Cigar Lake uranium deposit,Saskatchewan, Canada

The Cigar Lake U deposit is located in northern Saskatchewan in the eastern part of the Athabasca Sandstone Basin, and consists of a high-grade ore body (up to 55% U) located at a depth of ∼430 m. As part of a study to evaluate the analog features of this deposit with respect to a disposal vault for waste nuclear fuel, colloids (1–450 nm) and suspended particles (450nm) in groundwater have been investigated to evaluate their effect on element transport through the U deposit. Tangential-flow ultrafiltration was used to concentrate particles from 501 groundwater samples in order to characterize the size distribution, concentration, composition and natural radionuclide content of particles in representative parts of the U deposit. Although Cigar Lake groundwaters contain particles in all sizes ranging from 10 nm to slightly larger than 20 μm, most samples contained a relatively high concentration of colloids in the 100–400 nm size range. Particle compositions are similar to the composition of minerals in the sandstones and ore body, suggesting that particles in groundwater are generated by the erosion of fracture-lining minerals. As a result, particle concentrations in groundwater are affected by the integrity of the host rock. In some piezometers the high initial concentrations of suspended particles, which may have been drilling artifacts, decreased during the collection of the first 350 1. Although colloid concentrations fluctuated during sampling, there are no indications that these concentrations will be permanently reduced by continued groundwater pumping. The observed colloid and suspended particle concentrations in the deep groundwaters are too low to have a significant impact on radionuclide migration, provided that radionuclide sorption is reversible. If radionuclides are irreversibly sorbed to particles they cannot sorb to the host rock and their migration can only be evaluated with an understanding of particle mobility. The data for dissolved and particulate U, Th and Ra were used to calculate field-derived distribution ratios (R_d) between particles and groundwater. The wide range of observed R_d values indicates that these radionuclides in particulate form are not in equilibrium with groundwater. U-series isotope data indicated that most of the U and Ra on particles was derived from groundwater. Some particles could have retained their U for as long as 8000 a. The U and Ra contents of particles in the ore and surrounding clay zones are significantly higher than in particles from sandstone, suggesting that the clay has been an effective barrier to particle migration.     

桂北沙子江铀矿床沥青铀矿原位微区年代学和元素分析:对铀成矿作用的启示

微区原位分析是地球科学研究的重要手段,但这些分析技术在华南热液铀矿床中的应用相对较少,限制了对铀矿床成矿机理的深入认识。沙子江铀矿床是华南著名的花岗岩型热液铀矿床。本文利用电子探针(EMPA)、激光电感耦合等离子体质谱(LA-ICPMS)以及二次离子探针(SIMS)等微区原位分析技术,对沙子江铀矿床中的沥青铀矿开展了U-Pb同位素年代学及元素组成研究,确定了沥青铀矿的形成时代及成分特征,并探讨了蚀变作用对沥青铀矿成分及其表面年龄或化学年龄的影响。电子探针分析结果显示,该沥青铀矿以富铀和钙、极低含量的ThO_2和稀土元素为特征,揭示其为低温热液成因,成矿热液富含Ca。LA-ICP-MS分析结果显示,沥青铀矿的稀土元素总量较低,其配分模式呈轻稀土富集型,具有明显的负Eu异常,与赋矿围岩豆乍山花岗岩的稀土元素组成相似,暗示其铀源可能与豆乍山岩体有密切的关系。蚀变和未蚀变沥青铀矿成分的对比研究显示,蚀变作用会导致硅元素大量进入沥青铀矿晶格,造成铀和铅的丢失,从而影响沥青铀矿的表观年龄或化学年龄,但沥青铀矿的稀土元素配分模式不会受到蚀变的影响。未蚀变沥青铀矿的SIMS微区原位分析获得的U-Pb年龄为101. 3±4. 5Ma,表明沙子江铀矿床存在100Ma左右的铀成矿事件。受岩石圈伸展控制形成的富CO流体与富铀花岗岩相互作用浸取出花岗岩中的铀,并在合适的构造部位沉淀形成了沙子江铀矿床。     

Geochemical,isotopic, and geochronlologic constraints on the formation of the Eagle Point basement-hosted uranium deposit,Athabasca Basin,Saskatchewan, Canada and recent remobilization of primary uraninite in secondary structures

The Athabasca Basin hosts many world-class unconformity-related uranium deposits. Recently, uranium reserves for the Eagle Point basement-hosted deposit have increased with the discovery of new mineralized zones within secondary structures. A paragenetic study of Eagle Point reveals the presence of three temporally distinct alteration stages: a pre-Athabasca alteration, a main alteration and mineralization comprised of three substages, and a post-main alteration and mineralization stage that culminated in remobilization of uraninite from primary to secondary structures. The pre-Athabasca alteration stage consists of minor amounts of clinochlore, followed by dolomite and calcite alteration in the hanging wall of major fault zones and kaolinitization of plagioclase and K-feldspar caused by surface weathering. The main alteration and uranium mineralization stage is related to three temporally distinct substages, all of which were produced by isotopically similar fluids. A major early alteration substage characterized by muscovite alteration and by precipitation Ca–Sr–LREE-rich aluminum phosphate-sulfate minerals, both from basinal fluids at temperatures around 240°C prior to 1,600 Ma. The mineralization substage involved uraninite and hematite precipitated in primary structures. The late alteration substage consists of dravite, uranophane-beta veins, calcite veins, and sudoite alteration from Mg–Ca-rich chemically modified basinal fluids with temperatures around 180°C. The post-main alteration and mineralization stage is characterized by remobilization of main stage uraninite from primary to secondary structures at a minimum age of ca. 535 Ma. U–Pb resetting events recorded on primary and remobilized uraninites are coincident with fluid flow induced by distal orogenies, remobilizing radiogenic Pb to a distance of at least 225 m above the mineralized zones.     

Depositional characteristics of uranium tailings from Saskatchewan,Canada

The management of uranium tailings, generated as a by-product of ore processing, is particularly important to minimize the environmental footprint of the industry. A clear understanding of tailings slurry behavior is required at the time of deposition to help evaluate the storage capacity and life span of the containment facilities. The main purpose of this study was to investigate the segregation and self-weight settling properties of uranium tailings. Detailed laboratory investigations were conducted on tailings from 4, 5, and 6 % nominal mill feeds (high-grade McArthur River ores blended with special wastes on site) from the Cameco Key Lake operation. The results indicate that the three uranium tailings can be characterized as a sandy silt material with a negligible amount of clay. Their depositional behavior is governed by the initial solids content of the slurry. The investigated tailings showed insignificant segregation between 25 and 40 % initial solids content. The initial hydraulic conductivity during settling was about 10^?4 m/s at a void ratio of 4 and was increased by half an order of magnitude for the 4 % mill feed, and by almost two orders of magnitude for the 5 and 6 % mill feeds at a void ratio of 8. Over the same range of initial void ratio, the settling potential increased threefold: from 8 to 24 % for the 4 % mill feed and from 12 to 36 % for the 5 and 6 % mill feeds. The better rate and amount of dewatering of future high mill feed tailings as compared to the current low mill feed tailings means that the onsite containment facility can store more tailings thereby supporting a longer life span of the mill.     

Evaluation of the 210Po method at the Midwest uranium deposit,Northern Saskatchewan,Canada

Vertical profiles of ²¹⁰Po in soils near the Midwest uranium deposit and an associated surficial radioactive sandstone boulder train in northern Saskatchewan show a high ²¹⁰Po background in air-dried forest litter (24 pCi/g) and Ah horizon soil (11 pCi/g) relative to lower soil horizons (<1 pCi/g). These high levels mask the ²¹⁰Po signal from the radioactive boulders in the near-surface soil horizons. Only in the Bf and C horizons can the existence of the radioactive boulders be inferred from ²¹⁰Po determinations. For comparative purposes profiles for ²²⁶Ra, U, Ni, and other trace elements are also presented.Escape of most of the Rn from near surface soils into the atmosphere, homogenization and decay of Rn, and precipitation of decay products back onto surface soils satisfactorily explain the field observations discussed here.Compared to the highly anomalous ²²²Rn signal in soil gases over this boulder train the ²¹⁰Po contrast is very weak and is of little use for prospecting for this type of boulder train. The relatively high ²¹⁰Po background in surficial materials relative to lower soil horizons dictates that great care be taken with the ²¹⁰Po method; the deepest possible horizons should be sampled.     

Seasonal variations of helium,radon, and uranium in lake waters near the Key Lake uranium deposit,Saskatchewan

To test the usefulness of the He method for the detection of buried U ore, a lake-water survey of the Key Lake area was carried out during March 1977 and repeated in June 1977. A set of 87 lake-water samples from 37 sites in eight different lakes were collected from the same sites in each survey. These samples were analyzed for He, Rn, O₂, Eh, pH, conductivity, alkalinity, and U.In the lakes the highest He concentrations, of nearly four times atmospheric equilibrium concentrations, were obtained during the winter survey. This was under the ice in two bottom lake samples where the sandy overburden extends for some 50 m directly to the ore zone. Radon and U values at these sites were also anomalous, but the highest values of Rn and U were obtained in a shallow lake about 2 km south of the ore zone where concentrations of radioactive boulders occur.The average net He and Rn contents dropped from 21 standard nanolitres/litre (nl/l) and 25 picocuries/litre (pCi/l) in the winter under the ice to 3 nl/l and 8 pCi/l in the summer, respectively. Average U and conductivity dropped from 2.3 ppb and 15 μmho/cm to 1.5 ppb and 11 μmho/cm, respectively, in the same suites of samples. The drop in the ionic species probably reflects the effect of snow and ice meltwater dilution and the much larger drop in the dissolved He and Rn reflects the combined effects of meltwater dilution, wind turbulence over ice-free lakes, and change in thermal gradients.The He results must be viewed with guarded optimism until a detailed investigation is completed to ascertain what fraction of the detected He is from the ore, what fraction from basement He that may have found its way into the lakes via the fracture zone in which the ore is located, and what effect drilling has had on the He flow into the lakes from the ore zone.     

Distribution of arsenic and nickel in uranium mill tailings,Rabbit Lake,Saskatchewan, Canada

The Rabbit Lake U mine in-pit tailings management facility (TMF) is located in northern Saskatchewan, Canada. The tailings body is approximately 425 m long×300 m wide and 91 m thick at its centre. An investigation of the TMF was performed to collect tailings samples from depth to quantify the distribution of As and Ni in the tailings with respect to ore type and assess the distribution of As and Ni with respect to tailings mineralogy. The tailings body consists of alternating layers of ice, frozen tailings and unfrozen tailings which varied in texture from a slurry to a firm silty sand. The tailings solids are predominately composed of quartz (16–36%), calcium sulphate (0.3–54%) and illite (3 and 14%). Arsenic and Ni concentrations in the tailings show similar patterns with depth which were strongly related to historical changes in As and Ni concentrations in the mill feed. Mineralogy of the ore bodies indicated that As and Ni in the mill feed occurred primarily as 1:1 molar ratio arsenides such as niccolite and gersdorffite. Arsenic and Ni concentrations in the tailings were also measured at a near 1:1 molar ratio. Mill process records showed that an average of 71% of the As in the mill feed was solubilized during leaching. SEM analysis suggested that solubilized As is precipitated as Ca²⁺, Fe³⁺ and Ni²⁺ arsenates during the neutralization process. Mill records indicated that 17,000 tonnes of As were discharged to the TMF of which approximately 88% was as arsenates and 12% as primary arsenides.     

Controls on Ra during raffinate neutralization at the Key Lake uranium mill, Saskatchewan, Canada

This study was conducted to define the geochemical controls on ²²⁶Ra during raffinate (pH = 1.2) neutralization to pH 10 at the Key Lake U mill in northern Saskatchewan, Canada. High activities (120–150 Bq/L) of aqueous phase ²²⁶Ra are present in raffinate produced during milling of U ore. The solubility control of ²²⁶Ra in the SO₄-rich, hydrometallurgical raffinate solutions often involves the addition of BaCl₂ to form a radium-barite co-precipitate (Ba(Ra)SO₄). As such, neutralization experiments were conducted with samples of mill raffinate using Ca(OH)₂ or NaOH with and without the addition of BaCl₂. Radium-226 activity decreased from 150 to <4 Bq/L for all combinations of neutralizing agents with Ca(OH)₂ + BaCl₂ being the most effective combination (final activity ∼1.0 Bq/L; ∼99.3% removal). In the absence of BaCl₂, Ca(OH)₂ more efficiently removed ²²⁶Ra than NaOH between pH 4 and 8, due to the co-precipitation of ²²⁶Ra with gypsum. Overall, neutralization with the addition of BaCl₂ reduced ²²⁶Ra activities at lower pH values (by pH 4.5), due to co-precipitation of ²²⁶Ra with BaSO₄. At varying concentrations of BaCl₂, aqueous phase activities of ²²⁶Ra converged, but did not attain steady-state values during neutralization and would continue to decrease with time. Sequential extractions indicated that ²²⁶Ra in precipitates formed during neutralization of the mill raffinate is dominated by amorphous and crystalline Fe hydroxide phases, consistent with raffinate neutralization experiments that showed that adsorption onto ferrihydrite can remove most ²²⁶Ra in the raffinate. Data generated in this study are being used to define the long-term geochemical controls on ²²⁶Ra in U mill processes and tailings.     

Mineral chemistry and geochemistry of vanadian silicates in the Hemlo gold deposit,Ontario, Canada

Some of the most vanadium-rich silicate minerals known are present in green mica schist from the Hemlo gold deposit, Ontario, Canada. Vanadium-rich silicate minerals include green mica (up to 17.6 wt. % V₂O₃), phlogopite (10.1 wt. % V₂O₃), pumpellyite (25.7 wt. % V₂O₃), garnet (18.5 wt. % V₂O₃), epidote-group minerals (9.1 wt. % V₂O₃), antimonian vesuvianite (4.3 wt. % V₂O₃), and titanite (18.5 wt. % V₂O₅). In addition, minor amounts of V (<2 wt. % V₂O₃) are present in tourmaline, chlorite, talc and tremolite in other lithologies of the Hemlo deposit. The principal substitution that incorporates V into most of these silicate minerals is Al³⁺=V³⁺ in octahedral positions. Vanadium is incorporated into phlogopite mainly by the two substitutions: 3Mg²⁺ =2V³⁺+ and ^VIMg²⁺+^IVSi⁴⁺=^VIV³⁺ +^IVAl³⁺, and all of the three substitutions Ti⁴⁺+O^2- =V³⁺+(OH,F)^-, Ti⁴⁺=V⁴⁺, and 5Ti⁴⁺=4V⁵⁺ + may have operated in titanite.Vanadium-enriched green mica schist from the Hemlo gold deposit is characterized by uniform Ti/Zr ratios, systematically low Ti, Ni, Co and Sc abundances, and low levels of incompatible elements Th, U, Hf and Zr and is distinct in these respects from its Cr-enriched counterpart. These geochemical features, along with textural evidence (relict quartz and oligoclase phenocrysts), indicate that the V-enriched green mica schist from Hemlo was most likely derived mainly from quartz-oligoclase porphyry. However, its anomalously high V and Cr contents were probably introduced metasomatically from local maficultramafic sources and were fixed in green mica and oxides during the waning of a second regional metamorphism. Vanadium was further remobilized, and its concentration probably enhanced, during the late hydrothermal alteration, which resulted in the formation of the characteristic V-rich calc-silicate minerals.     

Aqueous alteration of the Bali CV3 chondrite: evidence from mineralogy, mineral chemistry, and oxygen isotopic compositions

A petrographic, geochemical, and oxygen isotopic study of the Bali CV3 carbonaceous chondrite revealed that the meteorite has undergone extensive deformation and aqueous alteration on its parent body. Deformation textures are common and include flattened chondrules, a well-developed foliation, and the presence of distinctive (100) planar defects in olivine. The occurrence of alteration products associated with the planar defects indicates that the deformation features formed prior to the episode of aqueous alteration. The secondary minerals produced during the alteration event include well-crystallized Mg-rich saponite, framboidal magnetite, and Ca-phosphates. The alteration products are not homogeneously distributed throughout the meteorite, but occur in regions adjacent to relatively unaltered material, such as veins of altered material following the foliation. The alteration assemblage formed under oxidizing conditions at relatively low temperatures (<100 degrees C). Altered regions in Bali have higher Na, Ca, and P contents than unaltered regions which suggests that the fluid phase carried significant dissolved solids. Oxygen isotopic compositions for unaltered regions in Bali fall within the field for other CV3 whole-rocks, however, the oxygen isotopic compositions of the heavily altered material lie in the region for the CM and CR chondrites. The heavy-isotope enrichment of the altered regions in Bali suggest alteration conditions similar to those for the petrographic type-2 carbonaceous chondrites.     

陕西华阳川铀铌矿床中铀矿物的年代学与矿物化学研究及其对铀成矿的启示

本文在详细的野外地质工作基础上,利用场发射扫描电镜(FE SEM)结合能谱分析(EDS)与电子探针分析(EMPA)等手段对华阳川铀铌矿床中主要铀矿物的种类、共生组合关系及铀矿物的矿物化学与年代学开展了详细的研究工作。研究成果显示,铀主要以铌钛铀矿的形式产出,其次为晶质铀矿。晶质铀矿的矿物学研究和电子探针年代学研究结果显示,矿床中存在两期晶质铀矿年龄,早期晶质铀矿的化学年龄为~201 Ma(印支期 燕山期之交),形成于岩浆 高温热液体系,并伴随大量早期蚀变的铌钛铀矿产出,为矿床形成的主要成矿期;晚期晶质铀矿的化学年龄为~129 Ma(燕山期),形成于高温热液体系,与少量未蚀变的铌钛铀矿产出,仅占次要地位,可能是区域内强烈的燕山期岩浆热液交代早期铌钛铀矿后,淋滤出的铀再次沉淀的结果。结合区域地质关系,认为早期的铀成矿可能主要与(霓辉石)黑云母方解石碳酸岩脉有成因联系,是矿床形成的重要时期;晚期的铀矿物可能只是区域内燕山期的岩浆热液交代早期铌钛铀矿后,铀被淋滤带出后再次在有利部位沉淀的结果。因此,华阳川铀铌矿床可能是一个主要形成于印支期 燕山期之交,并被燕山期岩浆活动(叠加)改造的与碳酸岩脉有关的铀铌矿床。     

加拿大萨斯喀彻温省索西(Southey)钾盐矿床特征及成因

加拿大萨斯喀彻温省索西(Southey)钾盐矿床,主要赋存于中泥盆统的Elk Point(埃尔克波因特)群上部Prairie Evaporite(草原蒸发岩)组。钾盐矿层稳定,似水平状展布,埋深约1250~1550 m;钾盐矿物主要有钾石盐(KCl)和光卤石(KCl·Mg Cl2·6H2O),矿石品位高,w(K2O)可达11.17%~21.85%,是世界少有的高品质钾盐矿床。文章分别从构造位置、古地理条件、物源补给、沉积韵律和成矿过程等多个方面综合分析了索西钾盐矿床的成因。     

Bromine and stable isotopic profiles of formation waters from potash mine-shafts, Saskatchewan, Canada

Sixty-five inflow samples from access shafts were collected at three separate potash mines in order to construct three 1000 m deep hydrochemical profiles. Bromine concentrations, and δD and δ¹⁸O stable isotopic compositions, increase with depth in each case. Measured isotopic ratios have not changed in 15+ years since the mine-inflows were first sampled, implying little change in the hydraulic regimes at the mines over time. However, the bromine concentrations are typically a factor of five lower than previously reported. Newer analytical techniques have improved the accuracy, precision and resolution of the hydrochemical profiles. Results indicate that the salinity of the inflow waters originated as mixtures of evaporatively concentrated seawater, meteoric water, and brine derived from halite dissolution. Extremely concentrated brines (TDS > 525 g/L) were found at the Cory and Allan potash mines some 55 km apart, but their role in the paleohydrogeology of the basin remains uncertain.     

The mineralogy of arsenic in uranium mine tailings at the Rabbit Lake In-pit Facility, northern Saskatchewan, Canada

 A detailed investigation of the mineralogy of As in the tailings of the Rabbit Lake uranium ore processing facility was conducted. The milling/ore extraction process was sampled at three different locations to obtain information about when, where and under what condition secondary As phases form. These samples were compared with four samples of varying As content from the Rabbit Lake in-pit tailings management facility (TMF). Up to 20% As in the tailings are present in primary minerals that reach the tailings directly because they are not dissolved during the uranium extraction. The remaining 80% constitute As that was dissolved during ore extraction and then re-precipitated before being discharged into the tailings pond. It was not possible to conclusively identify any individual re-precipitated (secondary) As minerals in the Rabbit Lake TMF. Indirect evidence from sequential extraction analyses suggests the presence of an amorphous Ca-As phase and a possible, but unlikely, minor amount of an amorphous Fe-As phase. However, the close association between hydrous ferric oxide (HFO) and As could be clearly demonstrated. HFO was identified to be 2-line ferrihydrite and its XRD pattern geometry indicates a substantial amount of adsorbed As. This is in good agreement with SEM, TEM and sequential extraction analyses that all showed the close association of HFO and As. Received: 14 February 2000 · Accepted: 9 May 2000     

粤北地区302矿床沥青铀矿的形成时代、地球化学特征及其成因研究

302铀矿床位于诸广山岩体东南部,是中国花岗岩型铀矿床中规模较大、埋藏较深的矿床。研究表明,沥青铀矿的U-Pb和Sm-Nd等时线年龄分别为(68.7±2.7)Ma和(70±11)Ma,与华南花岗岩型铀矿床的主成矿期一致。沥青铀矿低的εNd(t)值(-11.3～-13.1)、古老的Nd模式年龄(1.76～1.88Ga)以及它们的微量元素和稀土元素组成都与赋矿围岩油洞岩体,尤其与长江岩体十分相似,表明铀源可能主要来源于赋矿花岗岩体,尤其是长江岩体。     

Nd,Sr, Pb,Ar, and 0 isotopic systematics of Sturgeon Lake kimberlite,Saskatchewan, Canada: constraints on emplacement age,alteration, and source composition

Rb-Sr isotopic dating of phlogopite megacryst samples separated from Sturgeon Lake kimberlite, Saskatchewan, yields a crystallization age of 98±1 Ma (2 , MSWD=1.2; ⁸⁷Sr/⁸⁶Sr(t)=0.7059). The ⁴⁰Ar/³⁹Ar analyses of a phlogopite megacryst sample indicate the presence of large amounts of excess ⁴⁰Ar and yield an excessively old age of 410 Ma. Assessment of the Ar data using isotope correlation plots indicates clustering of the data points about a mixing line between the radiogenic ⁴⁰Ar component at 98 Ma and a trapped component with uniform ³⁶Ar/⁴⁰Ar and Cl/⁴⁰Ar. Values of {ie212-1} as high as +20%. (VSMOW) for calcite from the groundmass and a whole-rock sample indicate pervasive lowtemperature alteration. The {ie212-2} of matrix carbonate is-11.3%. (PDB), slightly lighter than typical values from the literature. The {ie212-3} values of about +5%. (VSMOW) for brown phlogopite megacrysts may be primary, green phlogopites are interpreted to be an alteration product of the brown variety and are 2%. heavier. Initial Nd-Sr-Pb isotopic ratios for a whole-rock sample {ie212-4}; ⁸⁷Sr/⁸⁶Sr=0.7063, ²⁰⁶Pb/²⁰⁴Pb=18.67, ²⁰⁷Pb/²⁰⁴Pb=15.54, ²⁰⁸Pb/²⁰⁴Pb=38.97) suggest an affinity with group I kimberlites. Initial {ie212-5} values of +1.7 and +0.5 (⁸⁷Sr/ ⁸⁶Sr(t)=0.7053 and 0.7050) for eclogitic and lherzolitic garnet megacryst samples, and values of 0.0 for two phlogopite megacryst samples reflect an origin from an isotopically evolving melt due to assimilation of heterogeneous mantle. Lilac high-Cr lherzolitic garnet megacrysts give an unusually high {ie212-6} of +28.6 (⁸⁷Sr/⁸⁶Sr=0.7046) indicating a xenocrystic origin probably from the lithospheric mantle. The very radiogenic ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb ratios of the kimberlite are consistent with melting of EM II (enriched) mantle components.     

Petrology of the Hara Lake paragneisses,northeastern Saskatchewan,Canada

Precambrian aluminous paragneisses in the Hara Lake area of northeastern Saskatchewan are characterized by the stable association of cordierite and garnet with either sillimanite or biotite; alkali feldspar is an important mineral of this association. The aluminous gneisses are interlayered with pyroxene-plagioclase gneisses that contain orthopyroxene, clinopyroxene, hornblende, and biotite. The gneisses in the study area and in the adjacent Charcoal Lake area were metamorphosed under conditions of the granulite facies. The petrologic evidence is consistent with a first metamorphic event during which the association sillimanite-biotite was stable, followed by a second event during which cordierite-garnet was stable. Consideration of mineral assemblages and mineral chemistries of the aluminous gneisses in terms of experimentally established or thermodynamically derived reactions suggests that recrystallization from the sillimanite-biotite association to cordierite-garnet took place at 680 °–750 °C and 3.2–4.4 kb.     

粤北棉花坑(302)铀矿床围岩蚀变分带的铀矿物研究

粤北棉花坑(302)铀矿床是华南最大的花岗岩型铀矿床。本文以该铀矿床的一个代表性钻孔岩心为研究对象,利用电子探针对该钻孔中的铀矿物进行系统研究。该钻孔岩心具有明显的垂直围岩蚀变分带现象:从上到下可分为四个带,分别为:正常花岗岩或弱蚀变带(Ⅰ带);高岭石化、绢云母化带(Ⅱ带);强绢云母化、绿泥石化带(Ⅲ带);矿化带(Ⅳ带)。铀矿物类型也具有分带现象:Ⅰ带、Ⅱ带、Ⅲ带的铀矿物主要是晶质铀矿和铀钍石;矿化带Ⅳ带的铀矿物主要有沥青铀矿、铀石、钛铀矿、铀钍石四种类型。运用电子探针测年方法对不同蚀变带的晶质铀矿和沥青铀矿进行定年,获得晶质铀矿的化学年龄为165±3.1Ma,代表长江岩体的形成年龄;沥青铀矿的化学年龄可分为四组:~120Ma、~102Ma、~92Ma和~68Ma,代表矿区多期次的热液活动时间,也可代表粤北地区多期次铀成矿作用年龄,前三组可能代表早期铀成矿事件,第四组为主成矿期。广泛发育的热液蚀变促使U发生活化、转移,进而在有利空间富集成矿。对典型铀矿床作深入细致的蚀变分带研究工作,有助于提高对成岩成矿过程的认识。     

Platinum-group minerals in fluid inclusions from the Marathon deposit,Coldwell Complex,Canada

Summary Platinum-group minerals (PGM) project into fluid inclusions that occur in chalcopyrite and cubanite from the Marathon deposit, Two Duck Lake gabbro, Coldwell Complex, Ontario. Semi-quantitative analyses of the micron-sized PGM were made by SEM-EDS; they reveal Ag-bearing intermetallic compounds of Pd₃Sn-Pd₃Pb-Pd₃Te (i.e., atokitezvyagintsevite-keithconnite) and telargpalite (Pd₂AgTe) on broken, irregular surfaces of the Cu-Fe-S minerals. Halite daughter minerals, and quenched brine occur in and around some opened fluid inclusions. These data confirm the hypothesis based on petrography and mineral compositions that saline fluids remobilized PGE, Cu, and other elements and precipitated them well after crystallization of sulfide and silicate magmas in the Marathon deposit.

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Platin-Gruppenminerale in Flüssigkeitseinschlüssen aus der Marathon Lagerstdtte, Coldwall Komplex, Kanada

Zusammenfassung Platin-Gruppenminerale (PGM) ragen in Flüzssigkeiteinschliisse, die im Kupferkies und Cubanit der Marathon Lagerstätte, Two Duke Lake Gabbro, Coldwell Komplex, Ontario, vorkommen, hinein. Semiqantitative Analysen der mikrongroßen PGM wurden mit einem SEM-EDS durchgeführt. Sie ergaben Ag-führende, intermetallische Verbindungen von Pd₃Sn-Pd₃Pb-Pd₃Te (Atokit-Zvyagintsevit-Keithconnit) und Telargpalit (Pd₂AgTe) auf zerbrochenen, irregulären Oberflächen der Cu-Fe-SMinerale. Steinsalz-Tochterkristalle und abgeschreckte Salzlösungen treten innerhalb und in der unmittelbaren Umgebung geöffneter Flüssigkeitseinschlüsse auf. Diese Daten bestätigen die Hypothese, basierend auf der Petrographie und der Mineralzusammensetzung, daß saline Fluida PGE, Cu und andere Elemente remobilisieren können, und daß d iese nach der Kristallisation der Sulfide und des Silikatmagmas in der Marathon Lagerstätte zur Ablagerung gekommen sind.

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With 3 Figures