The Role of Advective Fluid Flow and Diffusion during Localized, Solid-State Dehydration: Sondrum Stenhuggeriet, Halmstad, SW Sweden

A localized dehydration zone, Söndrum stone quarry, Halmstad,SW Sweden, consists of a central, 1 m wide granitic pegmatoiddyke, on either side of which extends a 2·5–3 mwide dehydration zone (650–700°C; 800 MPa; orthopyroxene–clinopyroxene–biotite–amphibole–garnet)overprinting a local migmatized granitic gneiss (amphibole–biotite–garnet).Whole-rock chemistry indicates that dehydration of the graniticgneiss was predominantly isochemical. Exceptions include [Y+ heavy rare earth elements (HREE)], Ba, Sr, and F, which aremarkedly depleted throughout the dehydration zone. Systematictrends in the silicate and fluorapatite mineral chemistry acrossthe dehydration zone include depletion in Fe, (Y + HREE), Na,K, F, and Cl, and enrichment in Mg, Mn, Ca, and Ti. Fluid inclusionchemistry is similar in all three zones and indicates the presenceof a fluid containing CO₂, NaCl, and H₂O components. Water activitiesin the dehydration zone average 0·36, or X_H2O = 0·25.All lines of evidence suggest that the formation of the dehydrationzone was due to advective transport of a CO₂-rich fluid witha minor NaCl brine component originating from a tectonic fracture.Fluid infiltration resulted in the localized partial breakdownof biotite and amphiboles to pyroxenes releasing Ti and Ca,which were partitioned into the remaining biotite and amphibole,as well as uniform depletion in (Y + HREE), Ba, Sr, Cl, andF. At some later stage, H₂O-rich fluids (H₂O activity >0·8)gave rise to localized partial melting and the probable injectionof a granitic melt into the tectonic fracture, which resultedin the biotite and amphibole recording a diffusion profile forF across the dehydration zone into the granitic gneiss as wellas a diffusion profile in Fe, Mn, and Mg for all Fe–Mgsilicate minerals within 100 cm of the pegmatoid dyke. KEY WORDS: charnockite; fluids; CO₂; brines; localized dehydration; Söndrum     

One dimensional diffusion of radiogenic 87Sr and fluid transport of volatile elements across the margin of a metamorphosed Archaean basic dyke from Saglek,Labrador

An example of diffusion in a natural solid rock is described using ⁸⁷Sr as a tracer. The distribution of excess radiogenic ⁸⁷Sr across the contact of a metamorphosed basic dyke in a granodioritic gneiss is shown to fit closely to a mathematically modelled theoretical diffusion curve. It is suggested that the excess radiogenic Sr was generated by the breakdown of older Rb-rich biotite in the country rock to form chlorite during a late-stage greenschist facies metamorphism, and then taken up into a fluid phase migrating along the country rock — dyke interface. This fluid introduced silica, alkalies, light REE, H₂O, CO₂, N and Cl into the marginal zone of the dyke, probably during fluid migration along grain boundaries. The present irregular distribution of the volatile constituents across the contact and in the dyke excludes a diffusion controlled distribution. The distribution of volatiles probably reflects the influence of the existing mineralogy on the geochemical anomaly actually recorded from a post magmatic process. Evidence is presented that the diffusivity of radiogenic Sr was enhanced by the presence of a volatile phase.     

Coexistence of a Fluid Phase with Granitic Magma: Geochemical Characteristics of REE and Cu in Miyako Granite and in Scheelite-bearing Aplitic Veins at the Yamaguchi Cu-W Skarn Deposit, Iwate, Japan

Abstract: The North granitic body of the Miyako pluton is located in the Northern Kitakami belt, Northeast Japan. The formation of the scheelite–chalcopyrite–magnetite–bearing aplitic veins and scheelite–chalcopyrite–magnetite–bearing Yamaguchi skarn deposit was closely associated with the formation of the Miyako plutons. Petrographic facies of the North granitic body vary from quartz diorite in marginal zone (zone A), to tonalite and granodiorite (zone B), and to granite (zone C) in the central. The large numbers of aplitic veins distributed around the Yamaguchi mining area are divided into two groups: barren and scheelite–mag–netite–chalcopyrite–bearing aplitic veins. The latter cut massive clinopyroxene skarns of the Yamaguchi deposit, and are composed of plagioclase, K‐feldspar and titanite. Some plagioclase crystals have dusty cores with irregularly shaped K‐feldspar flakes, and clear rims of albite. Textures of plagioclase in the mineralized aplitic veins are different from the idiomorphic textures with sharp plagioclase crystal boundaries that occur in the North granitic body and barren aplitic veins. These textural data suggest that the mineralized aplitic veins were formed from hydrothermal fluid. Changes in the contents of major and minor (Rb, Sr, Sc, Co, Th, U) elements in the North Miyako granitic body are similar to those of zoned plutons formed by typical magmatic differentiation processes. On the other hand, concentrations of REE, especially middle to heavy REE, of granitic rocks in zone C and barren aplitic veins are significantly lower than those of granitic rocks in zones A and B. The hypothetical chondrite‐normalized REE patterns, calculated assuming fractional crystallization from zone B granitic melt, suggest that REE concentrations of the residual melt increased with the degree of fractional crystallization, and changed into a pattern with enriched LREE and strongly negative Eu anomaly. However, the REE patterns of granitic rocks in zone C are different from the hypothetical patterns. Moreover, the REE patterns of magnetite–scheelite–chalcopyrite aplitic veins are quite different from those of granitic rocks. The Cu contents of granitic rocks in the North Miyako body increase from zone A (5–26 ppm) to zone B (10–26 ppm), and then clearly decrease to zone C (5–7 ppm) and drastically increase to the barren aplitic veins (39–235 ppm). Concentrations of Cu in the mineralized aplitic veins are also higher than those of the granitic rocks in zone C. The decrease in REE and Cu contents of granitic rocks from zone B to zone C is not a result of simple magmatic fractional differentiation. Fluid inclusions in quartz from mineralized aplitic veins contain 3.3 wt% NaCl equivalent and 5.8 wt% CO₂. It was also demonstrated experimentally that the removal of MREE and HREE by fluid from melt enabled the formation of complexes of REE and ligands of OH^‐ and CO₃^2‐. Based on the possibility that the melt of the granitic rocks of zone C and the mineralized aplitic veins coexisted with CO₂‐bearing fluid, it is thought that REE were extracted from the melt to the CO₂‐bearing fluid, and that the REE in the mineralized aplitic veins were transported by the CO₂‐bearing fluid. It is likely that the low HREE and Cu contents of the granitic rocks in zone C could have been caused by the removal of those elements from the granitic melt by the fluid coexisting with the melt. The expelled materials could have been the sources of scheelite–magnetite–chalcopyrite–bearing aplitic veins and copper mineralization of the Yamaguchi Cu‐W skarn deposit.     

Geochemistry of the Archean low- to high-grade transition zone,Southern India

The transition zone between Archean low- and high-grade rocks in southern India represents eroded crustal levels representative of 15–20 km. It is comprised chiefly of tonalitic gneisses with some varieties showing incipient charnockitization and of minor amounts of granitic gneiss and charnockite, both of which appear to have developed from the tonalitic gneisses.Tonalitic gneisses and charnockites are similar in major and trace elements composition while granitic gneisses are relatively enriched in Rb, K, Th, Ba and light rare earth element (REE) and depleted in Cr and Sc. All three rock types exhibit enriched light REE patterns with variable positive Eu anomalies. Total REE content decreases with increasing Eu/Eu and SiO₂ and with decreasing Fe₂O_3T and MgO in the tonalitic gneisses and charnockites.An internally consistent model for the production of the tonalitic gneisses involves partial melting of an enriched mafic source with variable ratios of hornblende to clinopyroxene. This source, in turn, is derived from an ultramafic mantle relatively enriched in incompatible elements. Granitic gneisses form from tonalitic gneisses by alkali metasomatism from chloride-bearing fluids with high H₂O/CO₂ ratios purged from the lower crust by CO₂, and charnockites are produced from tonalitic gneisses (and granitic gneisses) by ischochemical CO₂ metamorphism following the alkali metasomatism.     

Rare earth elements in metarhyolite dyke constraints on processes in a dynamic hydrothermal system,Um Ghannam,South Eastern Desert,Egypt

The Um Ghannam area lies within the core of Hafafit Complex, South Eastern Desert. This area is occupied mainly by granitic gneiss (orthogneiss). However, the granitic gneiss is extruded by swarm metarhyolite dykes and quartz veins. The studied metarhyolite dyke is classified into two distinctive zones. However, the intense degree of hydrothermal alteration can partition this dyke into weakly and extremely altered zones. According to the extraordinary diversity in color, this dyke is distinguished into gray to dark gray (weakly altered) and greenish (extremely altered) metarhyolite. Petrographical, mineralogical, and geochemical characteristics of the two distinctive zones are detected in a representative sample. Petrographically, the weakly altered zone is mainly represented by chloritization of primary biotite, garnet, and epidote, and argillitization of primary plagioclase. Although the extremely altered zone contains intensely altered remnants of the original rock, the extremely altered zone is distinguished by intense oxidation products (carbonate minerals and quartz, with significant amounts of secondary Cr-muscovite and hematite). The mineralogical studies are imposed on the millimeter and the micrometer scale in this important hydrogeothermal system. Except for Ca and Mg, most of the major elements are depleted at the extremely altered zone. However, the extremely altered zone is enriched in trace elements (Cr, Mn, Co, and Ni). The major elements of the extremely altered zone reflect the significant alterations (desilication, muscovitization, and carbonatization). These alteration processes have taken place in the hydrogeothermal system in the extremely altered zone. The geothermal fluid is responsible for these hydrothermal alterations. High fO₂ and high temperature are characteristic features of this fluid. Then, the high-field-strength elements such as Zr, Ti, and P are depleted as a significant hydrothermal alteration. Also, nuclear elements with the anion of (CO₃)^2? can travel as molecular complexes (carbonates), as long as the chemical and structural conditions are suitable for the movement of these elements from the metarhyolite dyke to redeposit and accumulate in another geologic formation. The rare earth elements La and Ce, as well as Yb and Lu, are partially mobilized during intensity alterations. The rare earth elements (REEs) are depleted in abundance with enrichment of CO₂ from the weakly altered zone to the extremely altered zone. The REE budget is decreased from the weakly altered zone to the extremely altered zone as 121.17 to (27.38???16.52), respectively. The significant depletion of ∑REEs is controlled by dissolution of monazite. Monazite breakdown and even apatite formation can be caused by alkaline fluid. This fluid is related to event and thermal stage. However, the negative anomaly of Eu can be noticed in all studied samples. Then, Eu anomaly may be formed from plagioclase fractionation. The weakly altered metarhyolite zone and orthogneiss have lower HREE/LREE (0.07–0.11), respectively, relative to the extremely altered metarhyolite zone (0.17???0.2). Even all studied samples at two significant zones are characterized by the enrichment of ∑LREEs relative to ∑HREEs.     

Evolution of gold-bearing veins in dykes of the Woods Point dyke swarm,Victoria

The Woods Point dyke swarm comprises hundreds of narrow, subparallel igneous dykes and dozens of pipe-shaped dyke bulges within strongly deformed early Palaeozoic turbidites of the Melbourne trough. Porpylitic alteration accompanied dyke emplacement and was followed by microfracturing induced by high fluid pressures, involving CO₂ of magmatic origin, as the dykes solidified. Further stress caused through-going faults having ladder and other patterns. Isotopic studies suggest that metamorphically or geothermally-derived solutions filled the faults and other fractures with quartz and carbonate and altered immediately adjacent dyke rock. However earlier-formed vein and wall rock carbonates retained their magmatic isotopic composition. Fluid inclusions indicate vein deposition began at approximately 400°C with salinities up to 9 weight percent NaCl. Nine sulfide minerals and gold were deposited in the veins after ankerite, sericite and albite, while quartz deposition continued through all stages. Sulfur isotopic determinations indicate the vein sulfur could not have been derived from adjacent sedimentary rocks, nor exclusively from the dykes. Metamorphic waters of marine origin is a viable source for sulfur. Saline and CO₂-rich alkaline solutions reacted with the dyke wall rocks and probably evolved chemically prior to deposition of gold. Vug carbonates deposited by meteoric water that leached vein carbonates mark the end of vein formation.Present Adress: 631 Station Street, North Carlton 3054, Victoria, Australia     

Fluid Characteristics and Evolution of the Zhawulong Granitic Pegmatite Lithium Deposit in the Ganzi‐Songpan Region,Southwestern China

The Zhawulong granitic pegmatite lithium deposit is located in the Ganzi-Songpan orogenic belt. Fluid inclusions in spodumene and coexisting quartz were studied to understand the cooling path and evolution of fluid within albite–spodumene pegmatite. There are three distinguishable types of fluid inclusions: crystal-rich, CO2–NaCl–H2O, and NaCl–H2O. At more than 500°C and 350~480 MPa, crystal-rich fluid inclusions were captured during the pegmatitic magma-hydrothermal transition stage, characterized by a dense hydrous alkali borosilicate fluid with a carbonate component. Between 412°C and 278°C, CO2–NaCl–H2Ofluid inclusions developed in spodumene (I) and quartz (II) with a low salinity (3.3–11.9 wt%NaCl equivalent) and a high volatile content, which represent the boundary between the transition stage and the hydrothermal stage. The subsequentNaCl–H2Ofluid inclusions from the hydrothermal stage, between 189°C and 302°C, have a low salinity (1.1–13.9 wt%NaCl equivalent). The various types of fluid inclusions reveal the P–T conditions of pegmatite formation, which marks the transition process from magmatic to hydrothermal. The ore-forming fluids from the Zhawulong deposit have many of the same characteristics as those from the Jiajika lithium deposit. The ore-forming fluid provided not only materials for crystallization of rare metal minerals, such as spodumene and beryl, but also the ideal conditions forthe growth of ore minerals. Therefore, this area has favorable conditions for lithium enrichment and excellent prospecting potential.     

Geochemistry of the Ilesha granite gneiss in the basement complex of southwestern Nigeria

The Ilesha granite gneiss comprises a varied series ranging from porphyroblastic alkali gneiss and granitic gneiss to banded and strongly foliated melanocratic rocks. Deformation is intense and the dominant structural trend is approximately N-S.Chemical data show essentially a systematic variation reflecting the differences in the petrographic character of the outcrops. SiO₂, Na₂O, K₂O and related trace elements, particularly Rb, are higher in the alkali and granitic varieties, whereas the melanocratic types have lower contents of these elements. The basic rocks are likewise significantly enhanced in TiO₂, Fe, MgO, CaO, Cr and Ni concentrations, with some values being comparable to those of basaltic rocks.     

Assimilation of the mafic‐ultramafic magma: a case study of diabase dyke at the Beidaihe,North China Craton

Assimilation serves as a significant part in magma's evolution. Because of rapid cooling of ultramafic‐mafic magma, assimilation between mantle‐derived magma and crustal rocks (wall‐rocks) is often neglected. The Beidaihe diabase dikes in North China Craton suggest that assimilation of the rapidly cooled mantle‐derived magma can not be ignored. The diabase dikes are very thin (0.5 to 2 m in width) and discordantly intrude into Ordovician limestone. Center of dyke is porphyritic texture while chilled margin of it is aphanitic texture, suggesting a rapid crystallization process. Moreover, limestone close to the dyke was transformed into marble because of contact‐thermal metamorphism. From the center to margin of the dykes, contents of SiO₂ (48.9→ 41.6 wt.%) and MgO (8.3 → 4.0 wt.%) are obviously decreased, but contents of CaO (6.4→8.3 wt.%) and CO₂ (0.8 → 5.2 wt.%) are distinctly increased. Meanwhile, calcites in the wall rocks adjacent to and far from the dykes are also greatly different. The calcites close to the dykes have high MgO and FeO contents but low CaO and CO₂ contents. All these suggest an assimilation process of the mantle‐derived magma with wall‐rock limestone. Calculating CO₂ contents in the dyke and wall rock suggest that the extent of assimilation is thought to reach up to 8 ‐ 12 %. Therefore, when the wall rocks of the mantle‐derived magma are carbonate rocks, its components are obviously influenced by assimilation, although it often rapidly chilled. Simultaneously, this study provides possible explanation for some mantle‐derived rocks in carbonate areas with high LOI.     

Dissolution and precipitation processes in deformed amphibolites: an example from the ductile shear zone of the Ryoke metamorphic belt, SW Japan

The granitic mylonite zone in the Cretaceous Ryoke metamorphic belt contains deformed amphibolites as thin layers. The amphibolite layers do not exhibit pinch‐and‐swell or boudinage structures, even when contained in a high‐strain granitic mylonite. This mode of occurrence suggests that they were deformed as much as the surrounding granite mylonite. In the highly deformed zone, strongly foliated amphibolites contain Ti‐rich brown amphibole porphyroclasts rimmed by Ti‐poor green amphibole, titanite and chlorite. These porphyroclasts are elongated, forming shear surfaces defined by preferential distribution of the chlorite and titanite. Porphyroclastic plagioclase in the strongly foliated amphibolites consists of two components: an anorthite‐rich core and an anorthite‐poor rim. Based on these observations, the mass‐balanced reaction occurring during deformation is defined as As the reaction products form a weak interconnected matrix, the strain rate of the amphibolites may be controlled by the rate of dissolution–precipitation through fluids. Weakly foliated amphibolites in the low‐strain zone exhibit cataclastic microstructures, whereas the strongly foliated amphibolites do not exhibit such features. These microstructural and chemical changes suggest that high‐strain amphibolites were initially deformed by cataclasis, followed by deformation through metamorphic reactions. During the metamorphism/deformation, old plagioclase grains with high X_an were not stable and dissolved, and new plagioclase grains with low X_an crystallized at the old plagioclase rim. Dissolution of old plagioclase and precipitation of new plagioclase occurred normal to and parallel to the foliation, respectively, reflecting incongruent pressure solution due to differential stress and changes in P–T–H₂O conditions. The development of incongruent pressure solution is attributed to increased fluid flux in the strongly foliated amphibolites, as evidenced by the greater abundance of hydration‐reaction products in the strongly foliated amphibolites than in the weakly foliated ones.     

Constraints on the timing and conditions of high‐grade metamorphism,charnockite formation and fluid–rock interaction in the Trivandrum Block,southern India

Incipient charnockites have been widely used as evidence for the infiltration of CO₂‐rich fluids driving dehydration of the lower crust. Rocks exposed at Kakkod quarry in the Trivandrum Block of southern India allow for a thorough investigation of the metamorphic evolution by preserving not only orthopyroxene‐bearing charnockite patches in a host garnet–biotite felsic gneiss, but also layers of garnet–sillimanite metapelite gneiss. Thermodynamic phase equilibria modelling of all three bulk compositions indicates consistent peak‐metamorphic conditions of 830–925 °C and 6–9 kbar with retrograde evolution involving suprasolidus decompression at high temperature. These models suggest that orthopyroxene was most likely stabilized close to the metamorphic peak as a result of small compositional heterogeneities in the host garnet–biotite gneiss. There is insufficient evidence to determine whether the heterogeneities were inherited from the protolith or introduced during syn‐metamorphic fluid flow. U–Pb geochronology of monazite and zircon from all three rock types constrains the peak of metamorphism and orthopyroxene growth to have occurred between the onset of high‐grade metamorphism at c. 590 Ma and the onset of melt crystallization at c. 540 Ma. The majority of metamorphic zircon growth occurred during protracted melt crystallization between c. 540 and 510 Ma. Melt crystallization was followed by the influx of aqueous, alkali‐rich fluids likely derived from melts crystallizing at depth. This late fluid flow led to retrogression of orthopyroxene, the observed outcrop pattern and to the textural and isotopic modification of monazite grains at c. 525–490 Ma.     

Production of metaluminous melt during fluid‐present anatexis: an example from the Maghrebian basement,La Galite Archipelago,central Mediterranean

Garnet brought to the surface by late Miocene granitoids at La Galite Archipelago (Central Mediterranean, Tunisia) contains abundant primary melt and fluid inclusions. Microstructural observations and mineral chemistry define the host garnet as a peritectic phase produced by biotite incongruent melting at ~800 °C and 0.5 GPa, under fluid‐present conditions. The trapped melt is leucogranitic with an unexpected metaluminous and almost peralkaline character. Fluid inclusions are one phase at room temperature, and contain a CO₂‐dominated fluid, with minor H₂O, N₂ and CH₄. Siderite and an OH‐bearing phase were identified by Raman and IR spectroscopy within every analysed inclusion, and are interpreted as products of a post‐entrapment carbonation/hydration reaction between the fluid and the host during cooling. The fluid present during anatexis is therefore inferred to have been originally richer in both H₂O and CO₂. The production of anatectic melt with a metaluminous signature can be explained as the result of partial melting of relatively Al‐poor protoliths assisted by CO₂‐rich fluids.     

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.     

The conditions of formation of sapphire and zircon in the areas of alkali-basaltoid volcanism in Central Vietnam

Study of the chemical composition of clinopyroxene and garnet megacrysts from the Dak Nong sapphire deposit and model calculations have shown that megacrysts originated from the crystallization of alkali basaltoid magma in a deep-seated intermediate chamber at 14–15 kbar, which is close to the Moho depth (50 km) in this part of southeastern Asia. The chamber was a source of heat and CO₂ fluids for the generation of crustal syenitic melts producing sapphires and zircons. The formation conditions of sapphires and zircons are significantly different. The presence of jadeite inclusions in placer zircons points to high pressures during their crystallization, which is confirmed by the ubiquitous decrepitation of CO₂-rich melt inclusions. Sapphires crystallized from iron-rich syenitic melt in the shallower Earth’s crust horizons with the participation of CO₂ and carbonate–H₂O–CO₂ fluids. The subsequent eruptions of alkali basalts favored the transportation of garnet and pyroxene megacrysts as well as sapphire and zircon xenocrysts to the surface. It is shown that sapphire deposits can be produced only during multistage basaltic volcanism with deep-seated intermediate chambers in the regions with thick continental crust. The widespread megacryst mineral assemblage (clinopyroxene, garnet, sanidine, ilmenite) and the presence of placer zircon megacrysts can be used as indicators for sapphire prospecting.     

A Study of Ore-forming Fluids in the Shimensi Tungsten Deposit, Dahutang Tungsten Polymetallic Ore Field, Jiangxi Province, China

The Dahutang tungsten polymetallic ore field is located north of the Nanling W-Sn polymetallic metallogenic belt and south of the Middle—Lower Yangtze River Valley Cu-Mo-Au-Fe porphyry-skarn belt.It is a newly discovered ore field,and probably represents the largest tungsten mineralization district in the world.The Shimensi deposit is one of the mineral deposits in the Dahutang ore field,and is associated with Yanshanian granites intruding into a Neoproterozoic granodiorite batholith.On the basis of geologic studies,this paper presents new petrographic,microthermometric,laser Raman spectroscopic and hydrogen and oxygen isotopic studies of fluid inclusions from the Shimensi deposit.The results show that there are three types of fluid inclusions in quartz from various mineralization stages:liquid-rich two-phase fluid inclusions,vapor-rich two-phase fluid inclusions,and three-phase fluid inclusions containing a solid crystal,with the vast majority being liquid-rich two-phase fluid inclusions.In addition,melt and melt-fluid inclusions were also found in quartz from pegmatoid bodies in the margin of the Yanshanian intrusion.The homogenization temperatures of liquid-rich two-phase fluid inclusions in quartz range from 162 to 363℃ and salinities are 0.5wt%-9.5wt%NaCI equivalent.From the early to late mineralization stages,with the decreasing of the homogenization temperature,the salinity also shows a decreasing trend.The ore-forming fluids can be approximated by a NaCl-H_2O fluid system,with small amounts of volatile components including CO_2,CH_4 and N_2,as suggested by Laser Raman spectroscopic analyses.The hydrogen and oxygen isotope data show that δ5D_(V-smow) values of bulk fluid inclusions in quartz from various mineralization stages vary from-63.8‰ to-108.4‰,and the δ~(18)O_(H2O) values calculated from the δ~(18)O_(V-)smow values of quartz vary from-2.28‰ to 7.21‰.These H-O isotopic data are interpreted to indicate that the ore-forming fluids are mainly composed of magmatic water in the early stage,and meteoric water was added and participated in mineralization in the late stage.Integrating the geological characteristics and analytical data,we propose that the ore-forming fluids of the Shimensi deposit were mainly derived from Yanshanian granitic magma,the evolution of which resulted in highly differentiated melt,as recorded by melt and melt-fluid inclusions in pegmatoid quartz,and high concentrations of metals in the fluids.Cooling of the ore-forming fluids and mixing with meteoric water may be the key factors that led to mineralization in the Dahutang tungsten polymetallic ore field.     

Ore‐Forming Fluids as Sampled by Sulfide‐ and Quartz‐Hosted Fluid Inclusions in the Jinwozi Lode Gold Deposit,Eastern Tianshan Mountains of China

The Jinwozi lode gold deposit in the eastern Tianshan Mountains of China includes auriferous quartz veins and network quartz veins that are exemplified by the Veins 3 and 210, respectively. This paper presents H‐, O‐isotope compositions and gas compositions of fluid inclusions hosted in sulfides and quartz, and S‐, Pb‐isotope compositions of sulfide separates collected from the principal Stage 2 ores in Veins 3 and 210. Fluid inclusions trapped in quartz and sphalerite are pseudo‐secondary and primary. They were trapped from the fluids during the successive or alternate precipitation of quartz with sulfides. H‐ and O‐isotope compositions of fluid inclusion of three pyrite and one quartz separates from Vein 210 plot within the field of degassed melt, which is evidence for the incorporation of magmatic fluid as well with some possibility of contribution of metamorphic water to the hydrothermal system since the two datasets show a higher oxygen isotopic ratio than those of degassed melt. However, δD and δ¹⁸O values of fluid inclusions hosted in sulfides and quartz from Vein 3 are distinctly lower than those from Vein 210. In addition, salinities of fluid inclusion from Vein 3, approximately 3 to 6 wt% NaCl equivalent, are considerably lower than those from Vein 210, which are approximately 8 to 14 wt% NaCl equivalent. Ore‐forming fluids of Veins 3 and 210 have migrated through the relatively high and low levels in the imbricate‐thrust column where rock deformation is characterized by dilatancy or ductile–brittle transition, respectively. Therefore, the ore‐forming fluid of Vein 3 is interpreted to have mixed with greater amounts of meteoric‐derived groundwater than that of Vein 210. Fluid inclusions hosted in sulfides contain considerably higher abundances of gaseous species of CO₂, N₂, H₂S, and so on, than those hosted in quartz. Many of these gaseous species exhibit linear correlations with H₂O. These linear trends are interpreted in terms of mixing between magmatic fluid and groundwater. The relative enrichment of gaseous species in fluid inclusions hosted in sulfides, coupled with the banded ore structure, suggests that the magmatic fluid was involved with the ore‐forming fluid in pulsation. Lead isotope compositions of 21 pyrite and galena separates form a linear trend, suggesting mixing of metallic materials from diverse reservoirs. The δ³⁴S values of pyrite and galena range from +5.6‰ to +7.9‰ and from +3.1‰ to +6.3‰, respectively, indicating sulfur of the Jinwozi deposit has been leached mainly from the granodiorite and partly from the Jinwozi Formation by the circulating ore‐forming fluid.     

The application of P–T–X(CO2) modelling in constraining metamorphism and hydrothermal alteration at the Damang gold deposit,Ghana

Orogenic gold mineralization at the Damang deposit, Ghana, is associated with hydrothermal alteration haloes around gold‐bearing quartz veins, produced by the infiltration of a H₂O–CO₂–K₂O–H₂S fluid following regional metamorphism. Alteration assemblages are controlled by the protoliths with sedimentary rocks developing a typical assemblage of muscovite, ankerite and pyrite, while intrusive dolerite bodies contain biotite, ankerite and pyrrhotite, accompanied by the destruction of hornblende. Mineral equilibria modelling was undertaken with the computer program thermocalc , in subsets of the model system MnO–Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–CO₂–H₂O–TiO₂–Fe₂O₃, to constrain conditions of regional metamorphism and the subsequent gold mineralization event. Metapelites with well‐developed amphibolite facies assemblages reliably constrain peak regional metamorphism at ~595 °C and 5.5 kbar. Observed hydrothermal alteration assemblages associated with gold mineralization in a wide compositional range of lithologies are typically calculated to be stable within P–T–X(CO₂) arrays that trend towards lower temperatures and pressures with increasing equilibrium fluid X(CO₂). These independent P–T–X(CO₂) arrays converge and the region of overlap at ~375–425 °C and 1–2 kbar is taken to represent the conditions of alteration approaching equilibrium with a common infiltrating fluid with an X(CO₂) of ~0.7. Fluid‐rock interaction calculations with M–X(CO₂) diagrams indicate that the observed alteration assemblages are consistent with the addition of a single fluid phase requiring minimum fluid/rock ratios on the order of 1.     

The P–T–X(fluid) evolution of meta‐anorthosites in the Eastern Granulites,Tanzania

Meta‐anorthosite bodies are typical constituents of the Neoproterozoic Eastern Granulites in Tanzania. The mineral assemblage (and accessory components) is made up of clinopyroxene, garnet, amphibole; scapolite, epidote, biotite, rutile, titanite, ilmenite and quartz. Within the feldspar‐rich matrix (70–90% plagioclase), mafic domains with metamorphic corona textures were used for P–T calculations. Central parts of these textures constitute high‐Al clinopyroxene – which is a common magmatic mineral in anorthosites – and is therefore assumed to be a magmatic relict. The clinopyroxene rims have a diopsidic composition and are surrounded by a garnet corona. Locally the pyroxene is surrounded by amphibole and scapolite suggesting that a mixed CO₂–H₂O fluid was present during their formation. Thermobarometric calculations give the following conditions for the metamorphic peak of the individual meta‐anorthosite bodies: Mwega: 11–13 kbar, 850–900 °C; Pare Mountains: 12–14 kbar, 850–900 °C; Uluguru Mountains: 12–14 kbar, 850–900 °C. The P–T evolution of these bodies was modelled using pseudosections. The amount and composition of the metamorphic fluid and <0.5 mol.% fluid in the bulk composition is sufficient to produce fluid‐saturated assemblages at 10 kbar and 800 °C. Pseudosection analysis shows that the corona textures most likely formed under fluid undersaturated conditions or close to the boundary of fluid saturation. The stabilities of garnet and amphibole are dependent on the amount of fluid present during their formation. Mode isopleths of these minerals change their geometry drastically between fluid‐saturated and fluid‐undersaturated assemblages. The garnet coronae developed during isobaric cooling following the metamorphic peak. The cooling segment is followed by decompression as indicated by the growth of amphibole and plagioclase. The estimated of the metamorphic fluid is ～0.3–0.5. Although the meta‐anorthosites have different formation ages (Archean and Proterozoic) they experienced the same Pan‐African metamorphic overprint with a retrograde isobaric cooling path. Similar P–T evolutionary paths are known from the hosting granulites. The presented data are best explained by a tectonic model of hot fold nappes that brought the different aged anorthosites and surrounding rocks together in the deep crust followed by an isobaric cooling history.     

河北滦平周台子条带状铁矿地质特征、围岩时代及其地质意义

河北滦平县周台子铁矿位于华北克拉通北缘,是产于前寒武纪单塔子群变质岩系中的鞍山式铁矿,具有条带状铁建造(BIF)特征。矿石主要呈条带状构造,有的呈条纹和致密块状构造。矿石类型主要以石英磁铁矿型为主,含铁介于30%~35%。前寒武纪变质岩是矿床的主要围岩,出露有黑云母(角闪)斜长片麻岩和斜长角闪岩,局部见花岗片麻岩。原岩恢复表明,黑云母(角闪)斜长片麻岩的原岩为英安岩-流纹岩,斜长角闪岩原岩为玄武岩。花岗片麻岩的SiO₂含量大于56%,MgO含量小于3%,Al₂O₃含量大于15%,Sr含量大于500×10^-6,Yb含量均小于1.9×10^-6,轻重稀土元素分异明显,重稀土元素强烈亏损,并且Eu负异常不明显,表明该片麻岩具埃达克质岩石的地球化学特征。锆石U-Pb定年结果显示出几组年龄,分别是2512±21Ma, 2452±9.6Ma,2394±55Ma。大体看,2512Ma代表了火山喷发和周台子铁矿BIF沉淀年龄,2452Ma左右的锆石年龄代表了TTG质花岗片麻岩的侵位结晶年龄,2394Ma锆石年龄代表了周台子铁矿经历了一次变质作用,并对原有的岩石和矿石进行了改造。锆石Hf同位素特征显示斜长角闪岩和TTG质片麻岩的岩浆源区受到过古老地壳物质的混染。周台子铁矿构造环境可能是与裂谷有关的张性环境。     

Genesis of the Xuebaoding W–Sn–Be Crystal Deposits in Southwest China: Evidence from Fluid Inclusions,Stable Isotopes and Ore Elements

The Xuebaoding crystal deposit, located in northern Longmenshan, Sichuan Province, China, is well known for producing coarse‐grained crystals of scheelite, beryl, cassiterite, fluorite and other minerals. The orebody occurs between the Pankou and Pukouling granites, and a typical ore vein is divided into three parts: muscovite and beryl within granite (Part I); beryl, cassiterite and muscovite in the host transition from granite to marble (Part II); and the main mineralization part, an assemblage of beryl, cassiterite, scheelite, fluorite, apatite and needle‐like tourmaline within marble (Part III). No evidence of crosscutting or overlapping of these ore veins by others suggests that the orebody was formed by single fluid activity. The contents of Be, W, Sn, Li, Cs, Rb, B, and F in the Pankou and Pukouling granites are similar to those of the granites that host Nanling W–Sn deposits. The calculated isotopic compositions of beryl, scheelite and cassiterite (δD, ?69.3‰ to ?107.2‰ and δ¹⁸O_H2O, 8.2‰ to 15.0‰) indicate that the ore‐forming fluids were mainly composed of magmatic water with minor meteoric water and CO₂ derived from decarbonation of marble. Primary fluid inclusions are CO₂? CH₄+ H₂O ± CO₂ (vapor), with or without clathrates and halites. We estimate the fluid trapping condition at T = 220 to 360°C and P > 0.9 kbar. Fluid inclusions are rich in H₂O, F^‐ and Cl^‐. Evidence for fluid‐phase immiscibility during mineralization includes variable L/V ratios in the inclusions and inclusions containing different phase proportions. Fluid immiscibility may have been induced by the pressure released by extension joints, thereby facilitating the mineralization found in Part III. Based on the geochemical data, geological occurrence, and fluid inclusion studies, we hypothesize that the coarse‐grained crystals were formed by: (i) the high content of ore elements and volatile elements such as F in ore‐forming fluids; (ii) occurrence of fluid immiscibility and Ca‐bearing minerals after wall rock transition from granite to marble making the ore elements deposit completely; (iii) pure host marble as host rock without impure elements such as Fe; and (iv) sufficient space in ore veins to allow growth.