爆裂法作为快速测定流体包裹体中二氧化碳（和其它气体）含量的手段及其在勘探中的使用：以中国山东和河北省金矿为例

The acoustic decrepitation method heats a small monomineralic sample and counts pressure impulses as the inclusions burst when they develop high internal pressures.For aqueous fluids,the decrepitation temperature is correlated with the homogenisation temperature,but gas rich fluids give a distinct and characteristic low temperature decrepitation peak which can be used to recognize gas rich fluid inclusions.This information is useful in exploration for Au deposits,which are frequently associated with CO_2 rich and sometimes CH_4 rich fluids. This distinctive decrepitation occurs because the CO_2 rich inclusion fluids expand according to the gas law and develop internal pressures high enough to burst the host mineral grain at temperatures well below their homogenisation temperatures.In contrast,aqueous fluids condense to a liquid and vapour phase during post-entrapment cooling.Upon subsequent heating their internal pressures do not increase significantly until after homogenisation to a single phase occurs and hence they do not decrepitate"prematurely"as gas rich inclusions do. This behaviour is usually regarded as an annoyance in conventional microthermometric homogenisation studies,but can readily be used as an exploration aid to find mineralisation deposited from such gas rich fluids.Decrepitation results on samples from Cowra Ck, NSW,Australia,which have also been microthermometrically measured for CO_2 content,show that amounts of less than 5 mole % CO_2 are easily distinguished by decrepitation and amounts as low as 1 mole % CO_2 may be determinable. Examples of the use of acoustic decrepitation in the study of 6 gold mines in the Shandong and Hebei provinces of China are discussed.     

A Textural and Mineralogical Study of the Shanzhuang Banded Iron Formation, Southeastern Margin of the North China Craton: Implications for the Overprint History of Hydrothermal Alteration and Supergenesis after Mineralization

The newly discovered Shanzhuang BIF is hosted in the Shancaoyu Formation of the Taishan Group within the Eastern Block, southeastern margin of the North China Craton. The ores can be subdivided into three types in terms of mineral assemblages, corresponding to three types (I, II, III). The element concentration of the type I magnetite is similar to that of the type II magnetite, while the type III magnetite is similar to that of the schist. In general, magnetite and hematite grains from the ores show high concentrations of Mn (1317, 1162 ppm), Co (787, 1023 ppm), Al (2224, 2435 ppm) and Ti (540, 300 ppm), Whereas magnetite is depleted in Si (420 ppm) and hematite enriched in Si (1690 ppm). Detailed petrographic and mineral chemical analysis of magnetite, hematite, amphibole/hornblende and pyroxene, reveals that almost all the minerals occur as subhedral-anhedral grains with pits and fractures, and the BIF is recrystallized to metamorphic assemblages of high amphibolite facies. Hornblende is highly enriched in Fe, Mg and Ca, but depleted in K and Na, mostly belonging to magnesiohornblende. In addition, the ratios of Mg/(Mg+Fe2+), Fe3+/(Fe3++Fe2+), Si/(Si+Ti+Al) and Al/Si are 0.48–0.64, 0.17–0.36, 0.79–0.88 and 0.14–0.27, respectively. It is suggested that hornblende is neither a typical magmatic origin nor a typical metamorphic. Pyroxene has the characteristics of high Ca and Fe, but low Ti and Al, with end-member components En, Wo and Fs in the ranges of 25.22–28.64 wt%, 43.71–46.40 wt% and 24.51–27.62 wt%, respectively, belonging to clinopyroxene, and mostly diopside, might be formed during the prograde metamorphism in the absence of H2O. The carbonate such as dolomite-ankerite series is probably a precursor mineral of the BIF deposit. Mass mineral chemical and structural characteristics indicate that the Shanzhuang iron deposit has been subjected to varying degrees of oxidized hydrothermal superimposed reformation, metamorphism, and supergenesis after mineralization, during which some elements have been migrated in some degree.     

Study on the Electrical Conductivity of 0.025 mol NaCl Solution at 0.25-3.75 GPa and 20-370℃

The electrical conductance of 0.025 mol NaCl solution was measured at0.25-3.75 GPa and 20-370℃. As shown by the results, the conductance increases with temper-ature, and there is a liner relation between the reciprocal of temperature and the logarithm ofthe conductance but their slopes are different at different pressures. The relations between theconductance and pressure is rather complex and there are some discontinuities: in the range of2.25-3.75 GPa, the conductance increases with the pressure; in the range of 1.25-2.0 GPa, theconductance is not related to the pressure; and at a pressure of 0.75 GPa, the conductance ishigher than that at the pressures nearby. This reflects that the NaCl solution has rather differentproperties of electronic chemistry at various pressures, and probably is an important cause forthe existence of the layers with high electrical conductance and low velocity in the Earth's crustand mantle.     

Symplectite of Pyrite and Magnetite in the Massive Sulphide Ore of the Mashan Mine,Anhui Province

A symplectite of pyrite and magnetite in the massive sulphide ore of the Mashan mine,Anhui Province,is interpreted to have been formed by their replacing earlier pyrrhotite.The compositions of pyrrhotite,pyrite and magnetite related to this texture are given by electron microprobe analysis.Such a texture is likely to be formed when the ore-forming system reaches the three-phase point of pyrrhotite,pyrite and magnetite from the pyrrhotite stability field.The very small probability for the system to reach this point could be used to account for the rare occurrence of such symplectite in natural ores.     

Stability and band gap engineering of silica-confined lead halide perovskite nanocrystals under high pressure

SiO₂is the major mineral substance in the upper mantle of the earth.Therefore,studies of the silica-coated materials under high-pressure are essential to explore the physical and chemical properties of the upper mantle.The silica-confined CsPbBr₃nanocrystals(NCs)have recently attracted much attention because of the improved photoluminescence(PL)quantum yield,owing to the protection of silica shell.However,it remains considerable interest to further explore the relationship between optical properties and the structure of CsPbBr₃@SiO₂NCs.We systemically studied the structural and optical properties of the CsPbBr₃@SiO₂NCs under high pressure by using diamond anvil cell(DAC).The discontinuous changes of PL and absorption spectra occurred at~1.40 GPa.Synchrotron X-ray diffraction(XRD)studies of CsPbBr₃@SiO₂NCs under high pressure indicated an isostructural phase transformation at about 1.36 GPa,owing to the pressure-induced tilting of the Pb-Br octahedra.The isothermal bulk moduli for two phases are estimated about 60.0 GPa and 19.2 GPa by fitting the equation of state.Besides,the transition pressure point of CsPbBr₃@SiO₂NCs is slightly higher than that of pristine CsPbBr₃NCs,which attributed to the buffer effect of coating silica shell.The results indicate that silica shell is able to enhance the stabilization without changing the relationship between optical properties and structure of CsPbBr₃NCs.Our results were fascinated to model the rock metasomatism in the upper mantle and provided a new‘lithoprobe’for detecting the upper mantle.     

Experimental Study on Water‐rock Reactions with CO2 Fluid in a Deep Sandstone Formation under High Temperature and Pressure

Qiongdongnan Basin has a tectonic geological background of high temperature and high pressure in a deep reservoir setting,with mantle-derived CO2.A water-rock reaction device was used under high temperature and high pressure conditions,in conjunction with scanning electron microscope(SEM)observations,to carry out an experimental study of the diagenetic reaction between sandstone at depth and CO2-rich fluid,which is of great significance for revealing the dissolution of deep clastic rock reservoirs and the developmental mechanism of secondary pores,promoting deep oil and gas exploration.In this study,the experimental scheme of the water-rock reaction system was designed according to the parameters of the diagenetic background of the deep sandstone reservoir in the Qiongdongnan Basin.Three groups of single mineral samples were prepared in this experiment,including K-feldspar samples,albite samples and calcite samples.Using CO2 as a reaction solution,a series of diagenetic reaction simulation experiments were carried out in a semi-closed high temperature and high pressure simulation system.A field emission scanning electron microscope(SEM)was used to observe the microscopic appearance of the mineral samples after the water-rock reaction,the characteristics of dissolution under high temperature and high pressure,as well as the development of secondary pores.The experimental results showed that the CO2-rich fluid has an obvious dissolution effect on K-feldspar,albite and calcite under high temperature and high pressure.For the three minerals,the main temperature and pressure window for dissolution ranged from 150℃to 300℃and 45 MPa to 60 MPa.Scanning electron microscope observations revealed that the dissolution effect of K-feldspar is most obvious under conditions of 150℃and 45 MPa,in contrast to conditions of200℃and 50 MPa for albite and calcite.Through the comparative analysis of experimental conditions and procedures,a coupling effect occurred between the temperature and pressure change and the dissolution strength and calcite.Under high temperature and high pressure,pressure changed the solubility of CO2,furthermore,the dissolution effect and strength of the sandstone components were also affected.The experiment revealed that high temperature and high pressure conditions with CO2-rich fluid has a significant dissolution effect on aluminosilicate minerals and is conducive to the formation of secondary pores and effective reservoirs.Going forward with the above understanding has important implications for the promotion of deep oil and gas exploration.     

Moessbauer and XRD characterization of contaminated sediments by coal mining drainage in Neath Canal, South Wales, UK

Sediment cores were collected from the upstream of the Neath Canal in South Wales and characterized for their mineral compositions and iron speciation in order to understand the influence of sedimentary properties on the contaminants of heavy metals. The sediments in the canal have been polluted by ocherous precipitate with heavy metals such as arsenic since a major mine water discharge in spring 1993. The sediment core was obtained just from the discharge point in the canal and distinguished into three layers in the field regarding to their physical properties including visible color, sediment particle composition and dryness. X-ray diffraction （XRD） and M6ssbauer spectroscopy revealed vertical variations of minerals and iron species in depth of the sediment profile. The upper layer, reddish-brown, is wet muddy precipitant and is very fine in particle size, consisting mainly of iron oxide and hydroxide. Arsenic is rich in this layer; probably the sorption on iron oxide surface is the main mechanism. The middle layer, 22.0-27.0 cm, is soft deposit in a yellow color and contains sheet silicate, calcite and goethite. The lower part below 27.0 cm is gray to dark gray in color and contains quartz, pyrite, coal particles that are much more similar to normal aquatic sediment. The upper two layers in brown and yellow colors as newly precipitated mud from AMD contain high concentrations of As, Ni under oxic conditions. The lower part as the old canal sediments under reducing conditions contains high Cu and Zn. Chromium is enriched in the limited part of the low layer, just beneath the boundary between the middle and low parts of the sedimentary column, where the redox conditions shifted from oxic to anoxic. It is clear that the distribution of these heavy metals is closely associated with the redox condition reflected in the iron speciation. Thus different treatments are necessary for each layer of the sediment since different mineral and geochemical properties of the sediment will give different impacts on the heavy metals.     

Seeing through the magnetite:Reassessing Eoarchean atmosphere composition from Isua(Greenland) ≥3.7 Ga banded iron formations

Estimates of early atmosphere compositions from metamorphosed banded iron formations(BIFs)including the well-studied ≥3.7 BIFs of the Isua supracrustal belt(Greenland)are dependent on knowledge of primary versus secondary Fe-mineralogical assemblages.Using new observations from locally well preserved domains,we interpret that a previously assumed primary redox indicator mineral,magnetite,is secondary after sedimentary Fe-clays(probably greenalite)±carbonates.Within ~3.7 Ga Isua BIF,pre-tectonic nodules of quartz+Fe-rich amphibole±calcite reside in a finegrained(≤100 μm)quartz+magnetite matrix.We interpret the Isua nodule amphibole as the metamorphosed equivalent of primary Fe-rich clays,armoured from diagenetic oxidative reactions by early silica concretion.Additionally,in another low strain lacunae,~3.76 Ga BIF layering is not solid magnetite but instead fine-grained magnetite+quartz aggregates.These magnetite+quartz aggregates are interpreted as the metamorphosed equivalent of Fe-clay-rich layers that were oxidised during diagenesis,because they were not armoured by early silicification.In almost all Isua BIF exposures,this evidence has been destroyed by strong ductile deformation.The Fe-clays likely formed by abiotic reactions between aqueous Fe~(2+)and silica.These clays along with silica±carbonate were deposited below an oceanic Fe-chemocline as the sedimentary precursors of BIF.Breakdown of the clays on the sea floor may have been by anaerobic oxidation of Fe~(2+),a mechanism compatible with iron isotopic data previously published on these rocks.The new determinations of the primary redoxsensitive Fe-mineralogy of BIF significantly revise estimates of early Earth atmospheric oxygen and CO_2 content,with formation of protolith Fe-rich clays and carbonates compatible with an anoxic Eoarchean atmosphere with much higher CO_2 levels than previously estimated for Isua and in the present-day atmosphere.     

Dynamics Analysis of the Baiyun Sag in the Pearl River Mouth Basin,North of the South China Sea

The Baiyun sag is a deep one developing on the slope of the Pearl River Mouth Basin. It occurs as a composite graben horizontally, and is composed of two sub-sags versus one low uplift. Vertically, the sedimentary architecture could be divided into three layers, i.e. the faulted layer on the bottom, the faulted-ductile stretching layer in the middle and the draping layer on the top. The main rifting stage of the sag is supposed to be characterized by ductile extension and thinning of the crust. The special deformation pattern is probably attributed to the fact that the Baiyun sag is located in the transfer zone of the pre-existing weak zone, which made the sag a strongly deformed area, characterized by the greatly thinned lithosphere and active magmatism. The highly rising mantle under the Baiyun sag should be an important mechanism responsible for the ductile deformation, which caused partial melting of the upper mantle. Upweiling to the upper crust and the sedimentary layers, the partial melting materials accommodated extensional strain and caused non-faulted vertical subsidence. Magma was collected under the transfer zone after the first stage of rifting, and transferred laterally in a direction perpendicular to the extension to the ENE and WSW parts of the sag and upwelled along the NW-trending basal faults, where WNW-trending shear faults developed in swarms. The faulting activity and sedimentation history of the Baiyun sag may have been affected by the ocean ridge jump around 24 Ma and the cessation of sea floor spreading around 16 Ma.     

On Deep Structures of the Xikang-Yunnan Axis

Through recent study, the author considers that the north-south-trending Kangding-Honghe tectonic belt is not a marginal uplift zone of the Yangtze Platform but a Tethyan-type collisional tectonic belt of which the crust-upper mantle can be structurally divided into three layers. The upper layer is the brittle upper crust, dominated by overthrusting and imbrication; the middle layer is the plastic lower crust and part of the upper mantle, represented by compression and shortening; and the lower layer is the upper mantle, probably belonging to the Yangtze Platform in light of the thickness of the lithosphere.     

Spatial Variations in Particle Size and Magnetite Concentration on Cedar Beach: Implications for Grain-Sorting Processes, Western Lake Erie, Canada

<正>This study examined spatial variations in the concentration,grain size and heavy mineral assemblages on Cedar Beach(Lake Erie,Canada).Magnetic studies of heavy mineral-enriched,dark-reddish sands present on the beach showed that magnetite(～150μm) is the dominant magnetic mineral.Surficial magnetic susceptibility values defined three zones:a lakeward region close to the water line(Zone 1),the upper swash zone(Zone 2) and the region landwards of the upper swash zone (Zone 3).Zone 2 showed the highest bulk and mass susceptibility(κ,χ) and the highest mass percentage of smaller grain-size(250μm) fractions in the bulk sand sample.Susceptibility(i.e.κandχ) values decreased and grain size coarsened from Zone 2 lakewards(into Zone 1) and landwards (into Zone 3),and correlated with the distribution of the heavy mineral assemblage,most probably reflecting preferential separation of large,less dense particles by waves and currents both along and across the beach.The eroded western section of Cedar Beach showed much higher concentrations of heavy minerals including magnetite,and finer sand grain sizes than the accreting eastern section, suggesting that magnetic techniques could be used as a rapid,cost-effective way of examining erosion along sensitive coastline areas.     

Major and Trace Elements of Magnetite from the Qimantag Metallogenic Belt: Insights into Evolution of Ore–forming Fluids

Magnetite, as a genetic indicator of ores, has been studied in various deposits in the world. In this paper, we present textural and compositional data of magnetite from the Qimantag metallogenic belt of the Kunlun Orogenic Belt in China, to provide a better understanding of the formation mechanism and genesis of the metallogenic belt and to shed light on analytical protocols for the in situ chemical analysis of magnetite. Magnetite samples from various occurrences, including the ore–related granitoid pluton, mineralised endoskarn and vein–type iron ores hosted in marine carbonate intruded by the pluton, were examined using scanning electron microscopy and analysed for major and trace elements using electron microprobe and laser ablation–inductively coupled plasma–mass spectrometry. The field and microscope observation reveals that early–stage magnetite from the Hutouya and Kendekeke deposits occurs as massive or banded assemblages, whereas late–stage magnetite is disseminated or scattered in the ores. Early–stage magnetite contains high contents of Ti, V, Ga, Al and low in Mg and Mn. In contrast, late–stage magnetite is high in Mg, Mn and low in Ti, V, Ga, Al. Most magnetite grains from the Qimantag metallogenic belt deposits except the Kendekeke deposit plot in the " Skarn " field in the Ca+Al+Mn vs Ti+V diagram, far from typical magmatic Fe deposits such as the Damiao and Panzhihua deposits. According to the(Mg O+Mn O)–Ti O2–Al2O3 diagram, magnetite grains from the Kaerqueka and Galingge deposits and the No.7 ore body of the Hutouya deposit show typical characteristics of skarn magnetite, whereas magnetite grains from the Kendekeke deposit and the No.2 ore body of the Hutouya deposit show continuous elemental variation from magmatic type to skarn type. This compositional contrast indicates that chemical composition of magnetite is largely controlled by the compositions of magmatic fluids and host rocks of the ores that have reacted with the fluids. Moreover, a combination of petrography and magnetite geochemistry indicates that the formation of those ore deposits in the Qimantag metallogenic belt involved a magmatic–hydrothermal process.     

Hydrothermal H?gbomite Associated with Vanadiferous-Titaniferous (V-Ti) Bearing Magnetite Bands in Bhakatarhalli Chromite Mine, Nuggihalli Greenstone Belt, Western Dharwar Craton, Karnataka, India

Hogbomite,a rare exotic mineral,is found to be associated with the vanadiferous-titaniferous （V-Ti） bearing magnetite bands at Bhakatarhalli,Nuggihaifi greenstone belt,western Dharwar Craton,India.We report on a second occurrence of hogbomite from the Dharwar craton in Karnataka,which is the sixth documented occurrence of this mineral from India.We evaluate the chemical characteristics of hogbomite and associated Fe-Ti-minerals in an attempt to identify its formation as a primary hydrothermal mineral in a metamorphosed magnetite layer.We report here the presence of hogbomite as a complex oxide of Fe,Mg,Al and Ti with accessory of Zn,V and Sn.Petrographic studies suggest the （V-Ti） bearing magnetite （Mt） contain spinel,hogbomite,chlorite,martite,ilmenite （Ⅱ） and minor amounts of diaspore.The hogbomite displays euhedral to subhedral textures,and is up to 250 μm along the grain boundaries of magnetite and ilmenite.In the samples studied,hogbomite is prismatic,irregular and elongated in shape.The genesis of hogbomite in veins between magnetite and ilmenite implies its precipitation from fluids without involving complicated reactions.Several models were proposed for the formation of hogbomite; however,the subject is still debatable.     

Hydrothermal Hgbomite Associated with Vanadiferous-Titaniferous(V-Ti) Bearing Magnetite Bands in Bhakatarhalli Chromite Mine,Nuggihalli Greenstone Belt,Western Dharwar Craton,Karnataka, India

Hgbomite, a rare exotic mineral, is found to be associated with the vanadiferous–titaniferous(V-Ti) bearing magnetite bands at Bhakatarhalli, Nuggihalli greenstone belt, western Dharwar Craton, India. We report on a second occurrence of hgbomite from the Dharwar craton in Karnataka, which is the sixth documented occurrence of this mineral from India. We evaluate the chemical characteristics of hgbomite and associated Fe-Ti-minerals in an attempt to identify its formation as a primary hydrothermal mineral in a metamorphosed magnetite layer.We report here the presence of hgbomite as a complex oxide of Fe, Mg, Al and Ti with accessory of Zn, V and Sn. Petrographic studies suggest the(V–Ti) bearing magnetite(Mt) contain spinel, hgbomite, chlorite, martite, ilmenite(Il) and minor amounts of diaspore. The hgbomite displays euhedral to subhedral textures, and is up to 250 μm along the grain boundaries of magnetite and ilmenite. In the samples studied, hgbomite is prismatic, irregular and elongated in shape. The genesis of hgbomite in veins between magnetite and ilmenite implies its precipitation from fluids without involving complicated reactions. Several models were proposed for the formation of hgbomite; however, the subject is still debatable.     

Geochemistry and Genesis of Iron-apatite Ore in the Khanlogh Deposit, Eastern Cenozoic Quchan-Sabzevar Magmatic Arc, NE Iran

The Khanlogh deposit in the Cenozoic Quchan-Sabzevar magmatic belt, NE Iran, is hosted by Oligocene granodioritic rock. The Khanlogh intrusive body is I-type granitoid of the calc-alkaline series. The orebodies are vein, veinlet, massive, and breccia in shape and occur along the fault zones and fractures within the host rock. Ore minerals dominantly comprise magnetite and apatite associated with epidote, clinopyroxene, calcite, quartz, and chlorite. Apatites of the Khanlogh deposit have a high concentration of REE, and show a strong LREE/HREE ratio with a pronounced negative Eu anomaly. Magnetites have a high concentration of REE and show weak to moderate LREE/HREE fractionation. They are comparable to the REE patterns in Kiruna-type iron ores and show an affinity to calc-alkaline magmas. The Khanlogh deposit is similar in the aspects of host rock lithology, alteration, mineralogy, and mineral chemistry to the Kiruna-type deposits. Field observations, hydrothermal alteration halos, style of mineralization, and the geochemical characteristics of apatite, magnetite, and host rock indicate that these magnetite veins have hydrothermal origin similar to Cenozoic Kiruna-type deposits within the Tarom subzone, NW Iran, and are not related to silica-iron oxide immiscibility, as are the major Precambrian magnetite deposits in central Iran.     

Assessment of Geological Security and Integrated Assessment Geo‐environmental Suitability in Worst‐hit Areas in Wenchuan Quake

Abstract: The Wenchuan earthquake in 2008 and geo-hazards triggered by the earthquake caused large injuries and deaths as well as destructive damage for infrastructures like construction, traffic and electricity. It is urgent to select relatively secure areas for townships and cities constructed in high mountainous regions with high magnitude earthquakes. This paper presents the basic thoughts, evaluation indices and evaluation methods of geological security evaluation, water and land resources security demonstration and integrated assessments of geo-environmental suitability for reconstruction in alp and ravine with high magnitude earthquakes, which are applied in the worst-hit areas (12 counties). The integrated assessment shows that: (1) located in the Longmenshan fault zone, the evaluated area is of poor regional crust stability, in which the unstable and second unstable areas account for 79% of the total; (2) the geo-hazards susceptibility is high in the evaluation area. The spots of geo-hazards triggered by earthquake are mainly distributed along the active fault zone with higher distribution in the moderate and high mountains area, in which the areas of high and moderate susceptibility zoning accounts for 40.1% of the total; (3) geological security is poor in the evaluated area, in which the area of the unsuitable construction occupies 73.1%, whereas in the suitable construction area, the areas of geological security, second security and insecurity zoning account for 8.3%, 9.3% and 9.3% of the evaluated area respectively; (4) geo-environmental suitability is poor in the evaluated area , in which the areas of suitability and basic suitability zoning account for 3.5% and 7.3% of the whole evaluation area.     

http://www.sciencedirect.com/science/article/pii/S1674987112000394

High-grade dehydration of amphibolite-facies rocks to granulite-facies is a process that can involve partial melting,fluid-aided solid-state dehydration,or varying degrees of both.On the localized meter scale,solid-state dehydration,due to CO₂-rich fluids traveling along some fissure or crack and subsequently outwards along the mineral grain boundaries of the surrounding rock,normally is the means by which the breakdown of biotite and amphibole to orthopyroxene and clinopyroxene occur.Various mineral textures and changes in mineral chemistry seen in these rocks are also seen in more regional orthopyroxene-clinopyroxene-bearing rocks which,along with accompanying amphibolite-facies rocks, form traverses of lower crust.This suggests that solid-state dehydration during high-grade metamorphism could occur on a more regional scale.The more prominent of these fluid-induced textures in the granulitefacies portion of the traverse take the form of micro-veins of K-feldspar along quartz grain boundaries and the formation of monazite inclusions in fluorapatite.The fluids believed responsible take the form of concentrated NaCl- and KC1- brines from a basement ultramafic magma heat source traveling upwards along grain boundaries.Additional experimental work involving CaSO₄ dissolution in NaCl-brines. coupled with natural observation of oxide and sulfide mineral associations in granulite-facies rocks,have demonstrated the possibility that NaCl-brines,with a CaSO₄ component,could impose the oxygen fugacity on these rocks as opposed to the oxygen fugacity being inherent in their protoliths.These results, taken together,lend credence to the idea that regional chemical modification of the lower crust is an evolutionary process controlled by fluids migrating upwards from the lithospheric mantle along grain boundaries into and through the lower crust where they both modify the rock and are modified by it. Their presence allows for rapid mass and heat transport and subsequent mineral genesis and mineral reequilibration in the rocks through which they pass.     

Geochronology and Geochemistry of the Mamupu Cu-Au Polymetallic Deposit, Eastern Tibet: Implications for Eocene Cu Metallogenesis in the Yulong Porphyry Copper Belt

The Mamupu skarn-type Cu-Au polymetallic deposit represents the first discovery of a medium deposit in the southern Yulong porphyry copper belt (YPCB), eastern Tibet. The Cu-Au mineralization mainly occurs as chalcopyrite in breccia, within the plate-like carbonate interlayer, being closely related to chloritization (e.g., chlorite, magnetite and epidote) and skarnization (e.g., diopside, tremolite and garnet). The ore-related quartz syenite porphyry (QSP) and granodiorite porphyry (GP) were emplaced at 40.1 ± 0.2 Ma and 39.9 ± 0.3 Ma, respectively. The QSP of Mamupu is an alkaline-rich intrusion, relatively enriched in LREE, LILE, depleted in HFSE, with no significant negative Eu and Ce anomalies, slightly high (87Sr/86Sr)i, low εNd(t), uniform (206Pb/204Pb)i and εHf(t) values, which indicates that the porphyry magma may be caused by both the mixing of metasomatized EM II enriched mantle and thickened juvenile lower crust. The QSP in the Mamupu deposit shares a similar genesis of petrology to other ore-related porphyries within the YPCB. High oxygen fugacity and water content of the magmas are essential for the formation of porphyry and skarn Cu deposits. The QSP has similar high magmatic oxidation states and water content to the Yulong deposit, which indicates that the Mamupu has a high prospecting potential. Differences in the geological characteristics and scale of mineralization between the Mamupu and other YPCB deposits may be due to the different emplacement depths of ore-related intrusions, as well as differences in the surrounding rocks.     

Mineral Association and Mineralogical Criteria for the Formation Conditions of A B—F—Sn—Bi Skarn in Damoshan,Gejiu Tin Field,Sothwest China

The Damoshan deposit is a small B-F-Sn Bi exoskarn deposit and contains a distinctive mineral assemblage comprising andradite,vesuvianite,calcite,diopside,magnetite,hematite,nordenskioldine,cassiterite,varlamoffite,schenfliesite,native bismuth,eulytite,bismite and bismuthite,in which the occurrence of eulytite is the first reported in China.Textures of the mineral paragenses show that andradite,vesuvianite and diopside were the earliest phases formed during metasomatism,i.e.,the skarn forming stage.Then nordenskioldine,magnetite and native bismuth,perhaps together with eulytite,were precipitated at the stage of retrograde alteration.The minerals varlamoffite,schoenfliesite,hematite ,bismite and bismuthite were probably the product of supergene alteration.The minerals were analyzed by means of electron microprobe.The data on the ,coexisting phases and their compositons show that during the metasomatism reduced F-and Sn-rich primary mineralizing solutions reacted with highly oxidized carbonated of the Gejie Formation,producing a high Fe^2 /Fe^3 skarn(vesuvianite-fluorite skarn)near the contact of granite,and a low Fe^2 /Fe^3 skarn(vesuvianite-fluorite skarn)near the contact of granite,and a low Fe^2 /Fe^3 skarn(andradite skarn)in the outer zone of the skarn body in which andradite is extremely tin-bearing up to 5.14 wt% SnO2),In the retrograde alteration stage ,B-rich,but F-and Si-deficient mineralizing solutions replaced the tin-bearing andradite,forming an association of nordenskioldine and magnetite,No sulphides were deposited at this stage because of the oxidization ambient conditions in the andradite skarn.In the spergene oxidation zone,the nordenskioldine was dissolved into varlmoffite and calcite,the native bismuth was transformed into bismite or bismuthite ,and the magnetite was altered into hematite under the action of the CO2-rich supergene solutions.     

Mechanism and kinetics of hydrothermal replacement of magnetite by hematite

The replacement of magnetite by hematite was studied through a series of experiments under mild hydrothermal conditions(140 -220℃, vapour saturated pressures) to quantify the kinetics of the transformation and the relative effects of redox and non-redox processes on the transformation. The results indicate that oxygen is not an essential factor in the replacement reaction of magnetite by hematite, but the addition of excess oxidant does trigger the oxidation reaction, and increases the kinetics of the transformation. However, even under high O_2(aq) environments, some of the replacement still occurred via Fe²⁺ leaching from magnetite. The kinetics of the replacement reaction depends upon temperature and solution parameters such as pH and the concentrations of ligands, all of which are factors that control the solubility of magnetite and affect the transport of Fe²⁺ (and the oxidant) to and from the reaction front. Reaction rates are fast at ~200℃, and in nature transport properties of Fe and,in the case of the redox-controlled replacement, the oxidant will be the rate-limiting control on the reaction progress. Using an Avrami treatment of the kinetic data and the Arrhenius equation, the activation energy for the transformation under non-redox conditions was calculated to be 26 ± 6 kJ mol^-1.This value is in agreement with the reported activation energy for the dissolution of magnetite, which is the rate-limiting process for the transformation under non-redox conditions.