Three mechanisms of ore re-mobilisation during amphibolite facies metamorphism at the Montauban Zn–Pb–Au–Ag deposit

The relative importance of mechanical re-mobilisation, hydrothermal dissolution and re-precipitation, and sulphide melting in controlling redistribution of metals during concurrent metamorphism and deformation is evaluated at the middle amphibolite facies Montauban deposit in Canada. As at many other deposits, ductile deformation was important in driving mechanical re-mobilisation of massive sulphides from limb regions into hinge regions of large-scale folds and is thus the most important for controlling the economics of Pb and Zn distribution. Two possible stages of hydrothermally driven re-mobilisation are discussed, each of which produces characteristically different alteration assemblages. Prograde hydrothermal re-mobilisation is driven by pyrite de-sulphidation and concurrent chlorite dehydration and is thus an internally driven process. At Montauban, the H₂S-rich fluid generated through this process allowed re-mobilisation of gold into the wall rock, where it was deposited in response to sulphidation of Fe Mg silicates. Retrograde hydrothermal re-mobilisation is an externally driven process, whereby large volumes of fluids from outside the deposit may dissolve and re-precipitate metals, and cause hydration of silicate minerals. This second hydrothermally driven process is not recognised at Montauban. Sulphide melting occurred as temperatures neared the peak metamorphic conditions. Melting initiated in the massive sulphides through arsenopyrite breakdown, and a small volume of melt was subsequently re-mobilised into the wall rock. Trace element partitioning and fractional crystallisation of this melt generated a precious metal-rich fractionate, which remained mobile until well after peak metamorphism. Thus, prograde hydrothermal re-mobilisation and sulphide melting were the most important mechanisms for controlling the distribution of Au and Ag.     

华南加里东期造山型金矿中金的来源—来自浙江诸暨陈蔡杂岩的证据

造山型金矿中金的来源是目前广泛争论的问题,尽管变质成因模式受到了较多的关注,但研究实例还不多。加里东期是华南地区重要的金矿成矿期,浙江诸暨陈蔡杂岩发育了从绿片岩相到角闪岩相的岩石组合,变质时代为加里东期,同时,其变质温度和压力等都已经得到精确厘定,为研究华南加里东期金矿形成与变质作用的关系提供理想的研究剖面对象。通过系统采集陈蔡杂岩岩石样品,在详细的岩相学研究的基础上对其中的黄铁矿中的金及亲硫元素进行了激光剥蚀-电感耦合-等离子体质谱（LA-ICP-MS）原位微区微量元素分析。研究结果表明：陈蔡杂岩角闪岩相岩石岩相学特征中有绿泥石,角闪石退变质为黑云母,反映退变质作用中有变质流体的回流。华南加里东期变质过程中,从绿片岩相到角闪岩相的相变过程中金及其他亲硫元素从主要赋存矿物黄铁矿中释放出来,进入变质流体,为江南造山带造山型金矿提供了金属来源。利用硫化物单矿物进行金的含量原位分析是解决变质过程中金活化迁移的重要手段。并提出华南加里东期变质过程中金的来源模式图。     

Texturally-early fluid inclusions in garnets: evidence of the prograde metamorphic path?

Well-formed, texturally-early fluid inclusions in garnets from the Archean Pikwitonei granulite domain, Manitoba, Canada, have been analyzed using microthermometric methods. The mean CO₂ homogenization temperature (to liquid) for inclusions in 12 of 13 samples from the Cauchon Lake-Nelson River area is +15.2° C (n=125, 2σ=8.2° C), corresponding to a CO₂ density of 0.82 g/cm³. Inclusions in the remaining sample have somewhat lower CO₂ homogenization temperatures (mean=+5.4° C, n=24). The studied inclusions contain an estimated 10 to 20 vol. percent H₂O, with minor amounts of other fluid species such as CH₄, N₂, and/or H₂S. The fluid inclusions were probably trapped during early garnet growth at relatively low pressures (≤5 kbar if at 750° C), and appear to have undergone only limited or possibly no subsequent re-equilibration. This interpretation is consistent with the “anti-clock-wise” P-T-t path (heating before loading) determined for the Pikwitonei region by other workers. For such a prograde path, inclusions entrapped early, at high temperatures but at relatively low pressures, would experience internal underpressures during most of the subsequent prograde and retrograde phases of metamorphism. The texturally-early fluid inclusions in garnets from the Pikwitonei region therefore cannot be used to provide direct information about the highest metamorphic temperature and pressure conditions (750° C and 7 kbar). However, the results obtained in this study suggest that texturally-early fluid inclusions in garnets may, in some cases, retain evidence of the prograde metamorphic path.     

造山型金矿研究进展:兼论中国造山型金成矿作用

造山型金矿指与大洋板块俯冲和陆块拼贴有关、产在汇聚板块边界变质地体内部或者边缘受韧-脆性断裂构造控制的,成矿流体以低盐度H2O-CO2-CH4为主要特征的,成矿深度(2~20 km)和温度(200~650℃)及其相应的蚀变矿化组合有较大变化的系列金矿床.造山型金矿形成与超大陆聚合时限具有一致性.由于围岩类型和控矿构造多样性、地球化学特征具有多解性、金属源区和演化的不确定性以及成矿就位和物质起源的空间差距,造山型金矿成因模式有以下两个主要观点.第一种为大陆地壳变质流体成因模式,认为造山型金矿形成于造山作用同变质阶段,并随岩石圈演化矿床的物质来源发生变化;富金流体的释放由上地壳岩石绿片岩相到角闪岩相的进变质作用导致,该过程中的黄铁矿向磁黄铁矿转变释放了大量的金,这种模式被广泛运用于赋存在绿片岩相中的显生宙造山型金矿.然而越来越多的实例证实造山型金矿主要形成于峰期变质的退变质阶段或者与区域变质没有任何关系,变质流体成因模式受到了强烈质疑;与大陆地壳变质模式相对立的是幔源流体模式,其认为流体起源于俯冲洋壳脱水或富集地幔再活化,不同时代和地区的成矿流体具有一致性;尽管该模式不符合传统的平衡条件下的相变原理,但是基于幔源流体的存在及其浅部运移的大量观测,初步认为成矿流体是在超临界和非平衡条件下完成了金属的幔→壳迁移.中国造山型金矿分布于江南造山带志留纪、天山-阿尔泰二叠纪、华北克拉通北缘三叠-侏罗纪、特提斯造山带二叠-侏罗纪、华南板块晚三叠世-侏罗纪、华北克拉通东南缘白垩纪、青藏高原及周缘古近纪等七大成矿带,主要受到了显生宙不同时代造山作用的控制,成矿时代晚于变质峰期,重要成矿带大型矿集区(胶东、哀牢山、扬子西缘)的实例解剖均支持幔源流体成因模式.     

Thermal and baric evolution of garnet granulites from Sri Lanka

Abstract Garnet granulites from Sri Lanka preserve textural and chemical evidence for prograde equilibration at temperatures of at least 700–750°C and pressures in the vicinity of 6–8 kbar. Associated strain patterns suggest prograde metamorphism occurred during and immediately following an episode of crustal thickening, with the prograde P–T conditions probably reflecting a combination of the conductive and advective transport of heat at the mid-levels of tectonically thickened crust. The occurrence of prograde wollastonite provides evidence for internally buffered fluid compositions, or fluid absent conditions, during peak metamorphism and precludes pervasive advection of a CO₂-rich fluid. The advective heat component is therefore likely to have been provided by the transport of silicate melt. Intricate symplectitic textures record partial re-equilibration of the garnet granulites to lower pressures (˜ 4–6 kbar) at high temperatures (600–750°C), and testify either to the erosional denudation of the overthick crust prior to significant cooling (i.e. quasi-isothermal decompression) or to a subsequent static heating possibly of early Palaeozoic age (Pan-African). The metamorphic history of the Sri Lankan granulites is compared with high grade terrains in the neighbouring fragments of Gondwana, with the emphasis on similarities with Proterozoic granulites of the East Antarctic craton.     

Evidence from mineral assemblages for infiltration of pelitic schists by aqueous fluids during metamorphism

Prograde mineral assemblages and compositions have been predicted for pelitic schist in the 10 component system Na₂O–K₂O–CaO–MnO–FeO–MgO–Al₂O₃–SiO₂–CO₂–H₂O for three cases of prograde metamorphism and fluid-rock interaction: (1) increasing temperature (T) at constant pressure (P) and constant pore fluid volume (1%) without infiltration (no-infiltration case); (2) increasing T at constant P accompanied by sufficient fluid infiltration that fluid composition is at all times constant (large-flux case); and (3) increasing T at constantP accompanied by a timeintegrated fluid flux f 10⁴ cm^{3 cm 2} (intermediate-flux case). Stable mineral assemblages and compositions were calculated by solving a system of non-linear equations that specify mass balance and chemical equilibrium between minerals and fluid. The model pelitic system includes quartz, muscovite, plagioclasc, chlorite, ankerite, siderite, biotite, garnet, staurolite, andalusite, kyanite, sillimanite, K-feldspar, and a coexisting, binary H₂O–CO₂ fluid. Specifically, prograde thermal metamorphism was modelled for Shaw's (1956) average low-grade pelite and for a moderate range of bulk rock compositions at P=3, 5, and 7 kb and initial fluids with Xco ₂ ^o =0.02–0.40. The model predicts a carbonate-bearing mineral assemblage for average pelite under chlorite zone conditions composed of quartz, muscovite, albite, chlorite, ankerite, and siderite. The mineral assemblages predicted for the noinfiltration case are unlike those typically observed in regional metamorphic terranes. Simulations of metamorphism for the large-flux and intermediate-flux cases, however, reproduce the sequence of mineral assemblages observed in normal Barrovian regional metamorphic terranes. These results suggest that regional metamorphism of pelitic schists is typically associated with infiltration of significant quantities of aqueous fluid.     

Effects of fluid production on fluid flow during regional and contact metamorphism

Numerical and analytical models of fluid flow that account for fluid production during prograde regional and contact metamorphism show that expulsion of metamorphic fluids dominates the convective flux when crustal permeabilities are less than 0.1–100 μD, depending primarily on the rate of fluid production. When this is the case, fluid circulation is limited or prevented, fluid pressures are elevated above hydrostatic values, and flow throughout most of the model is up and away from the region of maximum fluid production. Fluid circulation is predicted to occur where permeability is high, in dry rocks, or after rates of fluid production decrease as peak temperatures are reached. Large changes in the pattern of flow and influx of externally derived fluids may thus occur in metamorphic terranes when dehydration wanes or ceases and cooling begins. Inclusion of an impermeable horizon in the models further inhibits fluid circulation. Earlier, shallow hydrothermal models and interpretations based on the Rayleigh number may be inappropriate for characterizing fluid flow during prograde metamorphism at depth because they do not account for fluid production.     

辽宁红透山铜锌块状硫化物矿床的变质变形和成矿组分再活化

辽宁红透山铜-锌块状硫化物产在太古宙绿岩带中，矿床形成后经历了强烈的变形和变质，变质程度达高级角闪岩相。野外和显微镜研究表明，矿石在进变质过程中发生过强烈的机械再活化和重结晶，但各种进变质结构大部分已被变质峰期的全面重结晶所清除，目前保存着的结构主要是变质峰期和退变质过程的产物。退变质过程以黄铁矿变斑晶生长、矿石糜棱岩的形成、二次退火和化学再活化为特征。矿床中高度富集铜和金的矿石是韧性剪切形成的矿石糜棱岩受退变质流体叠加而成。磁黄铁矿主要是同生沉积后重结晶的产物，另有一部分由退变质热液形成，而黄铁矿变斑晶则有沉积一重结晶、磁黄铁矿退变质脱硫和热液叠加多种成因。世界各地块状硫化物矿床中的磁黄铁矿和黄铁矿各有三种成因类型。磁黄铁矿的类型有：同生沉积．变质重结晶、同生沉积黄铁矿变质和退变质热液充填或交代；黄铁矿的类型有：同生沉积-变质重结晶、磁黄铁矿退变质脱硫和退变质热液充填或交代。红透山矿区的退变质流体具有从早到晚氧逸度升高的趋势。     

Alpine metamorphism of calcareous metasediments in the Western Hohe Tauern,tyrol: mineral equilibria in COHS fluids

During Tertiary regional metamorphism in the Western Hohe Tauern, reaching maximum P, T conditions around 6 kb, 550° C in calcareous metasediments, reaction of pyrite to pyrrhotite is suggested by regional distribution and textural relations. In rocks without graphite pyrite is common at all metamorphic grades. In graphite bearing rocks, however, the dominant Fe-sulfide is pyrite at lower grade and pyrrhotite at higher grade. Furthermore, in graphite bearing high grade rocks, pyrite is restricted to assemblages with Mg-rich silicates. Several factors control pyrite-pyrrhotite relations. Increase of temperature is most effective by increase of pyrrhotite vs. pyrite stability field, shift of silicate-sulfide reactions toward the stability field of pyrrhotite, creation of sulfur free fluids from devolatilization reactions, and increase in the proportions of sulfur bearing fluid species. Presence of graphite also favours progress of pyrite to pyrrhotite reaction, as shown by different -stabilities and changes in the amount of minerals and fluid during metamorphic heating of graphite bearing and graphite free assemblages. An opposite effect is shown by assemblages with low Fe-contents in Fe-Mg silicates, due to the enlarged stability field of such minerals with increasing Mg (and F) content. Another inhibition of pyrite to pyrrhotite reaction is suggested to be due to relatively high sulfur contents of H₂O rich infiltrating fluids.     

Oxide and sulphide isograds along a Late Archean, deep-crustal profile in Tamil Nadu, south India

Oxide–sulphide–Fe–Mg–silicate and titanite–ilmenite textures as well as their mineral compositions have been studied in felsic and intermediate orthogneisses across an amphibolite (north) to granulite facies (south) traverse of lower Archean crust, Tamil Nadu, south India. Titanite is limited to the amphibolite facies terrane where it rims ilmenite or occurs as independent grains. Pyrite is widespread throughout the traverse increasing in abundance with increasing metamorphic grade. Pyrrhotite is confined to the high‐grade granulites. Ilmenite is widespread throughout the traverse increasing in abundance with increasing metamorphic grade and occurring primarily as hemo‐ilmenite in the high‐grade granulite facies rocks. Magnetite is widespread throughout the traverse and is commonly associated with ilmenite. It decreases in abundance with increasing metamorphic grade. In the granulite facies zone, reaction rims of magnetite + quartz occur along Fe–Mg silicate grain boundaries. Magnetite also commonly rims or is associated with pyrite. Both types of reaction rims represent an oxidation effect resulting from the partial subsolidus reduction of the hematite component in ilmenite to magnetite. This is confirmed by the presence of composite three oxide grains consisting of hematite, magnetite and ilmenite. Magnetite and magnetite–pyrite micro‐veins along silicate grain boundaries formed over a wide range of post‐peak metamorphic temperatures and pressures ranging from high‐grade SO₂ to low‐grade H₂S‐dominated conditions. Oxygen fugacities estimated from the orthopyroxene–magnetite–quartz, orthopyroxene–hematite–quartz, and magnetite–hematite buffers average 2.5 log units above QFM. It is proposed that the trends in mineral assemblages, textures and composition are the result of an external, infiltrating concentrated brine containing an oxidizing component such as CaSO₄ during high‐grade metamorphism later acted upon by prograde and retrograde mineral reactions that do not involve an externally derived fluid phase.     

Allochemical retrograde metamorphism in shear zones: an example in metapelites, Virginia, USA

Abstract Metapelites in the Altavista area, southwest Virginia Piedmont, USA, underwent allochemical hydrothermal retrograde metamorphism in synmetamorphic shear zones. The metapelites of the Evington Group were metamorphosed in a prograde sequence of chlorite, staurolite, and sillimanite zones. Garnet–biotite geothermometry and phase relations support eastward increasing metamorphic grade, ranging from 570° C in the staurolite zone to 650° C in the sillimanite zone at c. 5.8 kbar. Sillimanite-zone rocks later underwent progressive retrogression around shear zones which acted as fluid conduits. Retrograde assemblages are successively zoned around the shear zones with staurolite-, chloritoid- and kyanite-bearing assemblages. The shear zones commonly contain kyanite or tourmaline veins. Applicable phase equilibria indicate that retrogression occurred during isobaric cooling through c. 200–270° C. Rock compositional changes with retrogression occurred in steps: SiO₂ was gained in the early stages of the retrogression but lost in the late stages; Al₂O₃, K₂O, and H₂O were increasingly gained through the sequence; CaO was increasingly lost. Addition of H₂O and decreasing temperatures resulted in new ferromagnesian minerals (staurolite, chloritoid, chlorite) and changes in H₂O, SiO₂, Al₂O₃, K₂O, and CaO contents produced muscovite and sodic plagioclase. Subsequent to prograde metamorphism, deeply derived fluids migrated upwards along shear zones, providing fluid and energy for the retrograde reactions. The sheared rocks underwent fluid infiltration with fluid fluxes of 1.8 × 10⁷–4.3 × 10⁷ cm³/cm² corresponding to minimum estimated fluid-to-rock ratios of 7.5–21 as a function of position within the shear zone. Fluid flow was from high to low temperature early and low to high temperature later in the retrogression.     

Metamorphism in Archaean greenstone belts: calculated fluid compositions and implications for gold mineralization

An inescapable consequence of the metamorphism of greenstone belt sequences is the release of a large volume of metamorphic fluid of low salinity with chemical characteristics controlled by the mineral assemblages involved in the devolatilization reactions. For mafic and ultramafic sequences, the composition of fluids released at upper greenschist to lower amphibolite facies conditions for the necessary relatively hot geotherm corresponds to those inferred for greenstone gold deposits (X_CO2= 0.2–0.3). This result follows from the calculation of mineral equilibria in the model system CaO–MgO–FeO–Al₂O₃–SiO₂–H₂O–CO₂, using a new, expanded, internally consistent dataset. Greenstone metamorphism cannot have involved much crustal over-thickening, because very shallow levels of greenstone belts are preserved. Such orogeny can be accounted for if compressive deformation of the crust is accompanied by thinning of the mantle lithosphere. In this case, the observed metamorphism, which was contemporaneous with deformation, is of the low-P high-T type. For this type of metamorphism, the metamorphic peak should have occurred earlier at deeper levels in the crust; i.e. the piezothermal array should be of the ‘deeper-earlier’type. However, at shallow crustal levels, the piezothermal array is likely to have been of ‘deeper-later’type, as a consequence of erosion. Thus, while the lower crust reached maximum temperatures, and partially melted to produce the observed granites, mid-crustal levels were releasing fluids prograde into shallow crustal levels that were already retrograde. We propose that these fluids are responsible for the gold mineralization. Thus, the contemporaneity of igneous activity and gold mineralization is a natural consequence of the thermal evolution, and does not mean that the mineralization has to be a consequence of igneous processes. Upward migration of metamorphic fluid, via appropriate structurally controlled pathways, will bring the fluid into contact with mineral assemblages that have equilibrated with a fluid with significantly lower X_CO2. These assemblages are therefore grossly out of equilibrium with the fluid. In the case of infiltrated metabasic rocks, intense carbonation and sulphidation is predicted. If, as seems reasonable, gold is mobilized by the fluid generated by devolatilization, then the combination of processes proposed, most of which are an inevitable consequence of the metamorphism, leads to the formation of greenstone gold deposits predominantly from metamorphic fluids.     

Redistribution of trace elements during prograde metamorphism from lawsonite blueschist to eclogite facies; implications for deep subduction-zone processes

The transfer of fluid and elements from subducting crust to the overlying mantle wedge is a fundamental process affecting arc magmatism and the chemical differentiation of the Earth. While the production of fluid by breakdown of hydrous minerals is well understood, the liberation of trace elements remains generally unconstrained. In this paper, we evaluate the behaviour of trace elements during prograde metamorphism and dehydration using samples of high-pressure, low-temperature metamorphic rocks from New Caledonia. Samples examined include mafic and pelitic rock-types that range in grade from lawsonite blueschist to eclogite facies, and represent typical lithologies of subducting crust. Under lawsonite blueschist facies conditions, the low temperatures of metamorphism inhibit equilibrium partitioning between metamorphic minerals and allow for the persistence of igneous and detrital minerals. Despite this, the most important hosts for trace-elements include lawsonite, (REE, Pb, Sr), titanite (REE, Nb, Ta), allanite (LREE, U, Th), phengite (LILE) and zircon (Zr, Hf). At epidote blueschist to eclogite facies conditions, trace-element equilibrium may be attained and epidote (REE, Sr, Th, U, Pb), garnet (HREE), rutile (Nb, Ta), phengite (LILE) and zircon (Zr, Hf) are the major trace-element hosts. Chlorite, albite, amphibole and omphacite contain very low concentrations of the investigated trace elements. The comparison of mineral trace-element data and bulk-rock data at different metamorphic grades indicates that trace elements are not liberated in significant quantities by prograde metamorphism up to eclogite facies. Combining our mineral trace-element data with established phase equilibria, we show that the trace elements considered are retained by newly-formed major and accessory minerals during mineral breakdown reactions to depths of up to 150 km. In contrast, significant volumes of fluid are released by dehydration reactions. Therefore, there is a decoupling of fluid release and trace element release in subducting slabs. We suggest that the flux of trace elements from the slab is not simply linked to mineral breakdown, but results from complex fluid-rock interactions and fluid-assisted partial melting in the slab.Electronic Supplementary Material Supplementary material is available in the online version of this article at http://dx.doi.org/10.1007/s00410-003-0495-5.Editorial responsibility: J. Hoefs     

Subduction metamorphism of serpentinite‐hosted carbonates beyond antigorite‐serpentinite dehydration (Nevado‐Filábride Complex,Spain)

At sub‐arc depths, the release of carbon from subducting slab lithologies is mostly controlled by fluid released by devolatilization reactions such as dehydration of antigorite (Atg‐) serpentinite to prograde peridotite. Here we investigate carbonate–silicate rocks hosted in Atg‐serpentinite and prograde chlorite (Chl‐) harzburgite in the Milagrosa and Almirez ultramafic massifs of the palaeo‐subducted Nevado‐Filábride Complex (NFC, Betic Cordillera, S. Spain). These massifs provide a unique opportunity to study the stability of carbonate during subduction metamorphism at P–T conditions before and after the dehydration of Atg‐serpentinite in a warm subduction setting. In the Milagrosa massif, carbonate–silicate rocks occur as lenses of Ti‐clinohumite–diopside–calcite marbles, diopside–dolomite marbles and antigorite–diopside–dolomite rocks hosted in clinopyroxene‐bearing Atg‐serpentinite. In Almirez, carbonate–silicate rocks are hosted in Chl‐harzburgite and show a high‐grade assemblage composed of olivine, Ti‐clinohumite, diopside, chlorite, dolomite, calcite, Cr‐bearing magnetite, pentlandite and rare aragonite inclusions. These NFC carbonate–silicate rocks have variable CaO and CO₂ contents at nearly constant Mg/Si ratio and high Ni and Cr contents, indicating that their protoliths were variable mixtures of serpentine and Ca‐carbonate (i.e., ophicarbonates). Thermodynamic modelling shows that the carbonate–silicate rocks attained peak metamorphic conditions similar to those of their host serpentinite (Milagrosa massif; 550–600°C and 1.0–1.4 GPa) and Chl‐harzburgite (Almirez massif; 1.7–1.9 GPa and 680°C). Microstructures, mineral chemistry and phase relations indicate that the hybrid carbonate–silicate bulk rock compositions formed before prograde metamorphism, likely during seawater hydrothermal alteration, and subsequently underwent subduction metamorphism. In the CaO–MgO–SiO₂ ternary, these processes resulted in a compositional variability of NFC serpentinite‐hosted carbonate–silicate rocks along the serpentine‐calcite mixing trend, similar to that observed in serpentinite‐hosted carbonate‐rocks in other palaeo‐subducted metamorphic terranes. Thermodynamic modelling using classical models of binary H₂O–CO₂ fluids shows that the compositional variability along this binary determines the temperature of the main devolatilization reactions, the fluid composition and the mineral assemblages of reaction products during prograde subduction metamorphism. Thermodynamic modelling considering electrolytic fluids reveals that H₂O and molecular CO₂ are the main fluid species and charged carbon‐bearing species occur only in minor amounts in equilibrium with carbonate–silicate rocks in warm subduction settings. Consequently, accounting for electrolytic fluids at these conditions slightly increases the solubility of carbon in the fluids compared with predictions by classical binary H₂O–CO₂ fluids, but does not affect the topology of phase relations in serpentinite‐hosted carbonate‐rocks. Phase relations, mineral composition and assemblages of Milagrosa and Almirez (meta)‐serpentinite‐hosted carbonate–silicate rocks are consistent with local equilibrium between an infiltrating fluid and the bulk rock composition and indicate a limited role of infiltration‐driven decarbonation. Our study shows natural evidence for the preservation of carbonates in serpentinite‐hosted carbonate–silicate rocks beyond the Atg‐serpentinite breakdown at sub‐arc depths, demonstrating that carbon can be recycled into the deep mantle.     

阿尔泰大东沟铅锌矿的碳质流体及其成因

大东沟铅锌矿是阿尔泰南缘泥盆纪克朗火山-沉积盆地的块状硫化物矿床之一,在石炭—二叠纪同造山的区域变质过程中,受到热液叠加改造作用,层状铅锌矿体发育脉状石英和矿化。本文对阿勒泰大东沟铅锌矿区石英脉中的包裹体进行了详细的岩相学和显微测温研究,估算出包裹体形成时的物理化学条件,并采用激光拉曼、同步辐射X射线荧光(SRXRF)对流体包裹体进行了成分测试。结果显示,石英脉中的包裹体主要为碳质流体包裹体,多以面状、带状分布,最低捕获温度在209～459℃之间,密度为0.75～1.15g/cm3,最低捕获压力在110～540MPa之间。初步研究表明碳质流体的来源与同造山的变质作用有关,而与海底喷流沉积无关。激光拉曼测试结果表明包裹体气液主要成分为CO2和N2。SRXRF测试碳质包裹体中金属微量元素显示低Cu、Zn、Pb,而富集Au。     

http://www.sciencedirect.com/science/article/pii/S1674987115000900

The Chertovo Koryto gold deposit(80 t Au at 1.84 g/t) in the Lena world-class province,Siberia,is hosted in a metamorphosed sequence of the Paleoproterozoic Mikhailovsk Formation that comprises the oldest black shale strata of the Baikal-Patom region.The mineralisation is confined to the thrust zone complicated with a conjugate anticline fold,zones of shearing and dislocation.The struaural position of the mineralisation is similar to that at the giant Sukhoi Log deposit in the neighbouring Mama-Bodaibo zone.In the latter,the isotope age data suggest that Khomolkho black shales,hosts to Sukhoi Log mineralisation,are of Ediacaran age and underwent prograde metamorphism during early Paleozoic.The geochemical composition of the terrigenous rocks that host Sukhoi Log,Chertovo Koryto,and a number of other deposits at the various stratigraphic levels throughout the Proterozoic sequence have much in common.They do not show elevated metal contents above the common black shale abundances,except for Au and As,which is at variance with the accepted view on diagenetic enrichment of black shales in the Lena province.The occurrence of sagenitic rutile in quartz and chlorite pseudomorphs after biotite and other petrographic observations provide evidence on a retrograde nature of the metamorphic mineral assemblages in the Mikhailovsk rocks.The sulphides are pyrrhotite and arsenopyrite with very minor pyrite at Chertovo Koryto,whereas pyrite is the predominant sulphide in the Sukhoi Log ore.Fluid inclusion data on both deposits emphasise a high-temperature nature of the mineralisation albeit revealing great contrast in the fluid composition.Sukhoi Log mineralisation was formed at mixing between low-salinity aqueous solutions and dense gaseous carbonic fluids,which facilitated effective gold scavenging and precipitation,as demonstrated by thermodynamic simulation.The precursory devolatilisation of the Mikhailovsk sediments at the prograde stage results in the paucity of gaseous carbonic fluid during retrograde metamorphism and mineralisation.The similarity in the styles and chemical parameters of mineralisation,and the predominant structural control of ore localisation within the same Precambrian regional tectonic unit support an idea that orogenic gold mineralisation in the Lena province was produced during a single early Paleozoic event.     

Diagenesis and very low grade metamorphism in a 7,012?m-deep well Hongcan 1, eastern Tibetan plateau

This study uses clay mineral assemblages, illite ??crystallinity?? (IC), chlorite ??crystallinity?? (CC), illite polytypes, the b cell-dimension of K-white mica, mineral geothermo-geobarometers and homogenization temperatures of fluid inclusions to investigate the transition from diagenesis to metamorphism in a 7?km thick Triassic flysch sequence in the well Hongcan 1, eastern Tibetan plateau. The 7,012.8?m deep borehole penetrated flysch of Upper to the Middle Triassic age and represents a unique chance to characterize low temperature metamorphic processes in an unusually thick sedimentary sequence developed on thickened continental crust. Mineral assemblage analysis reveals a burial metamorphic pattern with kaolinite and chlorite/smectite mix-layer phases present in the upper 1,500?m, and illite/smectite mixed-layer phases extending to a depth of 3,000?m. The metamorphic index mineral, graphite, was detected in sedimentary rock below 5,000?m using Raman spectroscopy. There exists a good correlation between IC and CC within the prograde burial sequence; with CC anchizonal boundaries of 0.242 and 0.314°2?? (upper and lower boundaries, respectively) corresponding to Kübler??s IC limits at 0.25 and 0.42°2??. Illite polytypism also shows an increase in the 2M ₁ polytype with increasing depth, with ca. 60?% 2M ₁ abundance compared to the 1M type at the surface, to 100?% 2M ₁ at the bottom of the borehole. Fluid inclusion analysis show HHC-rich bearing fluids correspond to the diagenetic zone, CH₄-rich bearing fluids appear at transitional zone from diagenetic to low anchizone and H₂O-rich bearing fluids mark the high anchizone to epizone. Based on chlorite chemical geothermometer, calcite?Cdolomite geothermo-barometers as well as homogenization temperature of fluid inclusions, a paleotemperature range of 118?C348?°C is estimated for the well with a pressure facies of low to intermediate type.     

Metamorphic evolution of mineral assemblages in the layered unit and its host rocks of the eastern part of the Pana Massif,Kola Peninsula

The paper presents data on the mineral assemblages and chemical composition of minerals in rocks from the eastern part of the Pana Massif, Kola Peninsula, and the results obtained by studying the amphibolization of rocks of this massif genetically related to metamorphism. The rocks contain four amphibole populations, which can be used as good indicators for metamorphic facies. The amphiboles show broad compositional variability. Their evaluated P-T crystallization conditions indicate that the prograde stage of the overprinted metamorphic processes occurred at temperatures increasing from 382 to 473°C and pressures from 1.7 to 4.3 kbar. The retrograde stage (biotitization, chloritization, silification, and carbonatization) took place at temperatures of about 370°C and pressures of approximately 1 kbar. The fluid regime of the metamorphic transforms was also controlled by the temperature: the fluids were oxidizing early in the course of the process and gradually became more reducing with decreasing temperature.     

P-T-X parameters of metamorphogene and hydrothermal fluids,isotopy and age of the Bogunai gold deposit,southern Yenisei Ridge (Russia)

Fluid inclusions in quartz, sulfides from quartz veins, and quartz, garnet, plagioclase, and orthoclase from granulites of the Bogunai gold deposit located in the granulites of the Angara-Kan block of the Yenisei Ridge were studied by thermobarometry, gas chromatography, chromato-mass-spectrometry, Raman spectroscopy, and mass spectrometry with inductively coupled plasma. The formation temperatures (850-950 °C) and pressures (8.5-9.0 kbar) of minerals of the granulite metamorphic facies are much higher than the crystallization temperatures (220-420 °C) and pressures (0.1-1.6 kbar) of gold-quartz veins of the Bogunai deposit. These veins formed with the participation of H₂O-CO₂-hydrocarbon fluids with a salt (predominantly MgCl₂) concentration of 2-19 wt.% NaCl equiv. The gas phase of fluid inclusions from quartz, pyrite, chalcopyrite, galena, and sphalerite contains not only H₂O, CO₂, CH₄, and N₂ but also the first found compounds of sulfur (CS₂, O₂S, COS, C₂H6S₂) and nitrogen (C3H₇N, C3H₇NO, C₄H8N₂O) and numerous hydrocarbons of different classes (paraffins, arenes, naphthenes, alcohols, aldehydes, ketones, carbonic acids, and furans). The age of the Krasnoyarsk mineralized zone, one of the sites of the Bogunai deposit, is 466 ± 3.2-461.6 ± 3.1 Ma, which is almost 1400 Ma younger than the age of granulite metamorphism and 255 Ma younger than the age of diaphthoresis but is close to the age of the Lower Kan granitoid pluton (455.7 ± 3.4 Ma). The sulfur isotope ratios (5³⁴S) of sulfides (pyrite, chalcopyrite, sphalerite, and galena) are close to the mantle values, 0.8 to 3.5%c, and are in the range of the granitoid values, which indicates the crustal source of the fluid sulfur. Gold of the Bogunai deposit accumulated with the participation of H₂O-CO₂-hydrocarbon fluids generated both in deep-fault zones and in granitoid intrusions.     

Evolution of perthite composition and microstructure during progressive metamorphism of hypersolvus granite,Rhode Island,USA

The Scituate Granite in central Rhode Island, USA contains very coarse alkali feldspar mesoperthite and has been subjected to prograde metamorphism subsequent to original igneous cooling. The modal abundance and grain size of relics of alkali feldspar mesoperthite decrease systematically as metamorphic grade increases. The composition and microstructures of coexisting phases in the relict perthite grains also vary systematically with increasing metamorphic grade. Microstructures coarsen and become more complex, and compositions record increasing metamorphic temperatures.We suggest that the microstructures and compositions have been produced by exsolution, either during post-igneous cooling or early metamorphism, followed by partial homogenization during prograde metamorphism. The principal control on the evolution of the microstructures and compositions was probably the maximum temperature achieved during prograde metamorphism, with the abundance and size of perthite relics determined by recrystallization during deformation.