Origin of epithermal Ag–Au–Cu–Pb–Zn mineralization in Guanajuato, Mexico     

Helen Mango  Greg Arehart  Naomi Oreskes  Half Zantop 《Mineralium Deposita》2014,49(1):119-143

The Guanajuato epithermal district is one of the largest silver producers in Mexico. Mineralization occurs along three main vein systems trending dominantly northwest–southeast: the central Veta Madre, the La Luz system to the northwest, and the Sierra system to the east. Mineralization consists dominantly of silver sulfides and sulfosalts, base metal sulfides (mostly chalcopyrite, galena, sphalerite, and pyrite), and electrum. There is a broad zonation of metal distribution, with up to 10 % Cu+Pb+Zn in the deeper mines along the northern and central portions of the Veta Madre. Ore occurs in banded veins and breccias and as stockworks, with gangue composed dominantly of quartz and calcite. Host rocks are Mesozoic sedimentary and intrusive igneous rocks and Tertiary volcanic rocks. Most fluid inclusion homogenization temperatures are between 200 and 300 °C, with salinities below 4 wt.% NaCl equivalent. Fluid temperature and salinity decreased with time, from 290 to 240 °C and from 2.5 to 1.1 wt.% NaCl equivalent. Relatively constant fluid inclusion liquid-to-vapor ratios and a trend of decreasing salinity with decreasing temperature and with increasing time suggest dilution of the hydrothermal solutions. However, evidence of boiling (such as quartz and calcite textures and the presence of adularia) is noted along the Veta Madre, particularly at higher elevations. Fluid inclusion and mineralogical evidence for boiling of metal-bearing solutions is found in gold-rich portions of the eastern Sierra system; this part of the system is interpreted as the least eroded part of the district. Oxygen, carbon, and sulfur isotope analysis of host rocks, ore, and gangue minerals and fluid inclusion contents indicate a hydrothermal fluid, with an initial magmatic component that mixed over time with infiltrating meteoric water and underwent exchange with host rocks. Mineral deposition was a result of decreasing activities of sulfur and oxygen, decreasing temperature, increasing pH, and, in places, boiling.  相似文献   

Origin of the Yinshan epithermal-porphyry Cu–Au–Pb–Zn–Ag deposit,southeastern China: insights from geochemistry,Sr–Nd and zircon U–Pb–Hf–O isotopes     

《International Geology Review》2012,54(15):1835-1864

The Yinshan deposit is a large epithermal-porphyry polymetallic deposit, and the timing and petrogenesis of ore-hosting porphyries have been hotly debated. We present new results from geochemical, whole-rock Sr–Nd and zircon U–Pb–Hf–O isotopic investigations. Zircon U–Pb data demonstrate that the quartz porphyry, dacitic porphyry, and quartz dioritic porphyry formed at ?172.2 ± 0.4 Ma, ?171.7 ± 0.5 Ma, and ?170.9 ± 0.3 Ma, respectively. Inherited zircon cores show significant age spreads from ?730 to ?1390 Ma. Geochemically, they are high-K calc-alkaline or shoshonitic rocks with arc-like trace element patterns. They have similar whole-rock Nd and zircon Hf isotopic compositions, yet an increasing trend in ?_Nd(t) and ?_Hf(t) values typifies the suite. Older (inherited) zircons of the three porphyries display Hf compositions comparable to those of the Jiangnan Orogen basement rocks. In situ zircon oxygen isotopic analyses reveal that they have similar oxygen isotopic compositions, which are close to those of mantle zircons. Moreover, a decreasing trend of δ¹⁸O values is present. We propose that the ore-related porphyries of the Yinshan deposit were emplaced contemporaneously and derived from partial melting of Neoproterozoic arc-derived mafic (or ultra-mafic) rocks. Modelling suggests that the quartz porphyries, dacitic porphyries, and quartz dioritic porphyries experienced ?25%, ?10%, and ?10% crustal contaminations by Shuangqiaoshan rocks. Our study provides important constraints on mantle–crust interaction in the genesis of polymetallic mineralization associated with Mesozoic magmatism in southeastern China.  相似文献   

水泥–粉煤灰–煤渣–吹填粉细砂混合料强度试验     

温亮  阎长虹  张政  许宝田  张顺井  张东萍  周殷康 《煤田地质与勘探》2019,47(1):149

针对大型堆填场基层结构工程，本着就地取材节约成本的原则，利用吹填砂作为骨料，添加粉煤灰、煤渣和水泥，采用正交试验方法，编制正交设计表，配制不同比例的混合料进行无侧限抗压强度试验。采用方差对不同龄期的混合料抗压强度进行分析，并对混合料加固机理进行研究，给出了混合料最佳质量配比，即水泥20%，粉煤灰15%，煤渣10%，此时混合料的强度最大；其水泥掺量对混合料强度起着关键作用，随着龄期的增长粉煤灰与煤渣对混合料强度影响程度逐渐增强，不过煤渣对混合料初期强度影响不及粉煤灰。   相似文献   

Metallogeny of the northeastern Gangdese Pb–Zn–Ag–Fe–Mo–W polymetallic belt in the Lhasa terrane,southern Tibet     

《Ore Geology Reviews》2015

The northeastern Gangdese Pb–Zn–Ag–Fe–Mo–W polymetallic belt (NGPB), characterized by skarn and porphyry deposits, is one of the most important metallogenic belts in the Himalaya–Tibetan continental orogenic system. This belt extends for nearly four hundred kilometers along the Luobadui–Milashan Fault in the central Lhasa subterrane, and contains more than 10 large ore deposits with high potential for development. Three major types of mineralization system have been identified: skarn Fe systems, skarn/breccia Pb–Zn–Ag systems, and porphyry/skarn Mo–Cu–W systems. In this study, we conducted a whole-rock geochemical, U–Pb zircon geochronological, and in situ zircon Hf isotopic study of ore-forming rocks in the NGPB, specifically the Jiangga, Jiaduopule, and Rema skarn Fe deposits, and the Yaguila Pb–Zn–Ag deposit. Although some of these deposits (porphyry Mo systems) formed during the post-collisional stage (21–14 Ma), the majority (these three systems) developed during the main (‘soft collision’) stage of the India–Asia continental collision (65–50 Ma). The skarn Fe deposits are commonly associated with granodiorites, monzogranites, and granites, and formed between 65 and 50 Ma. The ore-forming intrusions of the Pb–Zn–Ag deposits are characterized by granite, quartz porphyry, and granite porphyry, which developed in the interval of 65–55 Ma. The ore-forming porphyries in the Sharang Mo deposit, formed at 53 Ma. The rocks from Fe deposits are metaluminous, and have relatively lower SiO₂, and higher CaO, MgO, FeO contents than the intrusions associated with Mo and Pb–Zn–Ag mineralization, while the Pb–Zn–Ag deposits are peraluminous, and have high SiO₂ and high total alkali concentrations. They all exhibit moderately fractionated REE patterns characterized by lower contents of heavy REE relative to light REE, and they are enriched in large-ion lithophile elements and relatively depleted in high-field-strength elements. Ore-forming granites from Fe deposits display ⁸⁷Sr/⁸⁶Sr_(i) = 0.7054–0.7074 and ε_Nd(t) = − 4.7 to + 1.3, whereas rocks from the Yaguila Pb–Zn–Ag deposit have ⁸⁷Sr/⁸⁶Sr_(i) = 0.7266–0.7281 and ε_Nd(t) = − 13.5 to − 13.3. In situ Lu–Hf isotopic analyses of zircons from Fe deposits show that ε_Hf(t) values range from − 7.3 to + 6.6, with T_DM(Hf)^C model ages of 712 to 1589 Ma, and Yaguila Pb–Zn–Ag deposit has ε_Hf(t) values from − 13.9 to − 1.3 with T_DM(Hf)^C model ages of 1216 to 2016 Ma. Combined with existing data from the Sharang Mo deposit, we conclude that the ore-forming intrusions associated with the skarn Fe and porphyry Mo deposits were derived from partial melting of metasomatized lithospheric mantle and rejuvenated lower crust beneath the central Lhasa subterrane, respectively. Melting of the ancient continental material was critical for the development of the Pb–Zn–Ag system. Therefore, it is likely that the source rocks play an important role in determining the metal endowment of intrusions formed during the initial stage of the India–Asia continental collision.  相似文献   

Formation of gold–silver sulfides and native gold in Fe–Ag–Au–S system     

G.A. Pal'yanova  K.A. Kokh  Yu.V. Seryotkin 《Russian Geology and Geophysics》2012,53(4):347-355

We carried out experiments on crystallization of Fe-containing melts FeS₂Ag_0.1–0.1xAu_0.1x (x = 0.05, 0.2, 0.4, and 0.8) with Ag/Au weight ratios from 10 to 0.1. Mixtures prepared from elements in corresponding proportions were heated in evacuated quartz ampoules to 1050 ºC and kept at this temperature for 12 h; then they were cooled to 150 ºC, annealed for 30 days, and cooled to room temperature. The solid-phase products were studied by optical and electron microscopy and X-ray spectroscopy. The crystallization products were mainly from iron sulfides: monoclinic pyrrhotite (Fe_0.47S_0.53 or Fe₇S₈) and pyrite (Fe_0.99S_2.01). Gold–silver sulfides (low-temperature modifications) are present in all synthesized samples. Depending on Ag/Au, the following sulfides are produced: acanthite (Ag/Au = 10), solid solutions Ag_2–xAu_xS (Ag/Au = 10, 2), uytenbogaardtite (Ag/Au = 2, 0.75), and petrovskaite (Ag/Au = 0.75, 0.12). They contain iron impurities (up to 3.3 wt.%). Xenomorphic micro- (<1–5 μm) and macrograins (5–50 μm) of Au–Ag sulfides are localized in pyrite or between the grains of pyrite and pyrrhotite. High-fineness gold was detected in the samples with initial ratio Ag/Au ≤ 2. It is present as fine and large rounded microinclusions or as intergrowths with Au–Ag sulfides in pyrite or, more seldom, at the boundary of pyrite and pyrrhotite grains. This gold contains up to 5.7 wt.% Fe. Based on the sample textures and phase relations, a sequence of their crystallization was determined. At ~1050 ºC, there are probably iron sulfide melt L₁ (Fe,S ? Ag,Au), gold–silver sulfide melt L₂ (Au,Ag,S ? Fe), and liquid sulfur L_S. On cooling, melt L₁ produces pyrrhotite; further cooling leads to the crystallization of high-fineness gold (macrograins from L₁ and micrograins from L₂) and Au–Ag sulfides (micrograins from L₁ and macrograins from L₂). Pyrite crystallizes after gold–silver sulfides by the peritectic reaction FeS + L_S = FeS₂ at ~743 ºC. Elemental sulfur is the last to crystallize. Gold–silver sulfides are stable and dominate over native gold and silver, especially in pyrite-containing ores with high Ag/Au ratios.  相似文献   

The Fe–C–O–H–N system at 6.3–7.8 GPa and 1200–1400 °C: implications for deep carbon and nitrogen cycles     

Alexander?G.?SokolEmail authorView author&#;s OrcID profile  Anatoly?A.?Tomilenko  Taras?A.?Bul’bak  Alexey?N.?Kruk  Pavel?A.?Zaikin  Ivan?A.?Sokol  Yurii?V.?Seryotkin  Yury?N.?Palyanov 《Contributions to Mineralogy and Petrology》2018,173(6):47

Interactions in a Fe–C–O–H–N system that controls the mobility of siderophile nitrogen and carbon in the Fe⁰-saturated upper mantle are investigated in experiments at 6.3–7.8 GPa and 1200–1400 °C. The results show that the γ-Fe and metal melt phases equilibrated with the fluid in a system unsaturated with carbon and nitrogen are stable at 1300 °C. The interactions of Fe₃C with an N-rich fluid in a graphite-saturated system produce the ε-Fe₃N phase (space group P6₃/mmc or P6₃22) at subsolidus conditions of 1200–1300 °C, while N-rich melts form at 1400 °C. At IW- and MMO-buffered hydrogen fugacity (fH₂), fluids vary from NH₃- to H₂O-rich compositions (NH₃/N₂?>?1 in all cases) with relatively high contents of alkanes. The fluid derived from N-poor samples contains less H₂O and more carbon which mainly reside in oxygenated hydrocarbons, i.e., alcohols and esters at MMO-buffered fH₂ and carboxylic acids at unbuffered fH₂ conditions. In unbuffered conditions, N₂ is the principal nitrogen host (NH₃/N₂?≤?0.1) in the fluid equilibrated with the metal phase. Relatively C- and N-rich fluids in equilibrium with the metal phase (γ-Fe, melt, or Fe₃N) are stable at the upper mantle pressures and temperatures. According to our estimates, the metal/fluid partition coefficient of nitrogen is higher than that of carbon. Thus, nitrogen has a greater affinity for iron than carbon. The general inference is that reduced fluids can successfully transport volatiles from the metal-saturated mantle to metal-free shallow mantle domains. However, nitrogen has a higher affinity for iron and selectively accumulates in the metal phase, while highly mobile carbon resides in the fluid phase. This may be a controlling mechanism of the deep carbon and nitrogen cycles.  相似文献   

LA–ICP–MS U–Pb定年技术相关问题探讨     

李艳广  靳梦琪  汪双双  吕鹏瑞 《西北地质》2023,(4):274-282

LA–ICP–MS U–Pb定年技术是地质科学中被广泛应用的重要手段。发展至今，该技术已相对成熟，但在实际工作中仍需要注意一些关键问题。笔者就该技术的样品准备、定年结果的取舍、铅丢失问题、普通铅问题和定年结果投图与解释等5个方面进行简要探讨。研究认为，对于复杂矿物进行U–Pb定年研究建议不分选出单矿物，而是采用矿物识别定位手段和LA–ICP–MS仪器相结合的技术手段，直接在岩石光片或探针片上进行原地原位微区定年分析，但要注意样品准备过程中可能存在的铅污染问题。在碎屑矿物定年结果选择方面，对于大于1.5Ga的定年测点，笔者建议采用₂₀₇Pb/₂₀₆Pb年龄代表该颗粒的结晶年龄，而对于小于1.5 Ga的定年测点则应采用₂₀₆Pb/₂₃₈U年龄。对沉积岩最大沉积年龄的判断和选择主要依靠统计学方法，必要时需要结合地球化学数据和地质背景信息作为辅助判断依据。对于连续分布在谐和线上的年轻样品要提高警惕，需要采用谐和图、加权平均图、CL图像和元素含量等多种手段识别是否存在铅丢失不一致线。针对普通铅校正问题，笔者重...  相似文献   

Melting of Fe–Ni–Si and Fe–Ni–S alloys at megabar pressures: implications for the core–mantle boundary temperature     

Guillaume Morard  Denis Andrault  Nicolas Guignot  Julien Siebert  Gaston Garbarino  Daniele Antonangeli 《Physics and Chemistry of Minerals》2011,38(10):767-776

High pressure melting behavior of three Fe-alloys containing 5 wt% Ni and (1) 10 wt% Si, (2) 15 wt% Si or (3) 12 wt% S was investigated up to megabar pressures by in situ X-ray diffraction and laser-heated diamond anvil cell techniques. We observe a decrease in melting temperature with increasing Si content over the entire investigated pressure range. This trend is used to discuss the melting curve of pure Fe. Moreover, our measurements of eutectic melting in the Fe–Fe₃S system show a change in slope around 50 GPa concomitant with the fcc–hcp phase transition in pure solid iron. Extrapolations of our melting curve up to the core–mantle boundary pressure yield values of 3,600–3,750 K for the freezing temperature of plausible outer core compositions.  相似文献   

Nd–Sr–Hf–O isotope provinciality in the northernmost Arabian–Nubian Shield: implications for crustal evolution     

Y. Be’eri-Shlevin  Y. Katzir  J. Blichert-Toft  I. C. Kleinhanns  M. J. Whitehouse 《Contributions to Mineralogy and Petrology》2010,160(2):181-201

Multi-isotope study including whole-rock Nd–Sr, single zircon Hf, and SIMS δ¹⁸O analyses of zircons sheds light on magma sources in the northernmost Arabian–Nubian Shield (ANS) during ~820–570 Ma. Reconnaissance initial Nd and Sr isotope data for the older rocks (~820–740 Ma) reaffirms previous estimates that early crustal evolution in this part of the shield involved some crustal contamination by pre-ANS material. Prominent isotope provinciality is displayed by post-collisional calc-alkaline and alkaline igneous rocks of ~635–570 Ma across a NW-SE transect across basement of the Sinai Peninsula (Egypt) and southern Israel. Silicic rocks of the NW-region are characterized by lower εNd(T)–εHf(T) and higher Sr_i and δ¹⁸O compared with rocks of the SE-region, and the transition between the regions is gradual. Within each region isotope ratios are independent of the extent of magma fractionation, and zircon cores and rims yield similar δ¹⁸O values. Comparison with southern segments of the ANS shows that the source for most ~635–570 Ma rocks can be modeled as the isotopically aged lower-intermediate crust in the ANS core (SE-region) and its northern, more contaminated ANS margins (NW-region). Nevertheless, Nd–Sr isotope enrichment of the lithospheric mantle is indicated by some basic magmas of the NW-region displaying the most enriched Nd–Sr isotope compositions. Comparison of Nd and Hf depleted mantle model ages for rocks of the SE-region may indicate that crustal formation events in the ANS geographical core took place at 1.1–1.2 Ga and were followed by crustal differentiation starting at ~0.9 Ga.  相似文献   

The molar volume of FeO–MgO–Fe2O3–Cr2O3–Al2O3–TiO2 spinels     

Emily A. Hamecher  Paula M. Antoshechkina  Mark S. Ghiorso  Paul D. Asimow 《Contributions to Mineralogy and Petrology》2013,165(1):25-43

We define and calibrate a new model of molar volume as a function of pressure, temperature, ordering state, and composition for spinels in the supersystem (Mg, Fe²⁺)(Al, Cr, Fe³⁺)₂O₄ ? (Mg, Fe²⁺)₂TiO₄. We use 832 X-ray and neutron diffraction measurements performed on spinels at ambient and in situ high-P, T conditions to calibrate end-member equations of state and an excess volume model for this system. The effect on molar volume of cation ordering over the octahedral and tetrahedral sites is captured with linear dependence on Mg²⁺, Al³⁺, and Fe³⁺ site occupancy terms. We allow standard-state volumes and coefficients of thermal expansion of the end members to vary within their uncertainties during extraction of the mixing properties, in order to achieve the best fit. Published equations of state of the various spinel end members are analyzed to obtain optimal values of the bulk modulus and its pressure derivative, for each explicit end member. For any spinel composition in the supersystem, the model molar volume is obtained by adding excess volume and cation order-dependent terms to a linear combination of the five end-member volumes, estimated at pressure and temperature using the high-T Vinet equation of state. The preferred model has a total of 9 excess volume and order-dependent parameters and fits nearly all experiments to within 0.02 J/bar/mol, or better than 0.5 % in volume. The model is compared to the current MELTS spinel model with a demonstration of the impact of the model difference on the estimated spinel-garnet lherzolite transition pressure.  相似文献   

Fluid entrapment and reequilibration during subduction and exhumation: A case study from the high-grade Nestos shear zone, Central Rhodope, Greece     

Kurt Krenn  Christoph Bauer  Alexander Proyer  Evripidis Mposkos  Georg Hoinkes 《Lithos》2008,104(1-4):33-53

A fluid inclusion study on metamorphic minerals of successive growth stages was performed on highly deformed paragneisses from the Nestos Shear Zone at Xanthi (Central Rhodope), in which microdiamonds provide unequivocal evidence for ultrahigh-pressure (UHP) metamorphism. The correlation of fluid inclusion density isochores and fluid inclusion reequilibration textures with geothermobarometric data and the relative chronology of micro- and macro-scale deformation stages allow a better understanding of both the fluid and metamorphic evolution along the P–T–d path. Textural evidence for subduction towards the NE is recorded by the orientation of intragranular NE-oriented fluid inclusion planes and the presence of single, annular fluid inclusion decrepitation textures. These textures occur within quartz “foam” structures enclosed in an earlier generation of garnets with prolate geometries and rarely within recrystallized matrix quartz, and reequilibrated both in composition and density during later stages of exhumation. No fluid inclusions pertaining to the postulated ultrahigh-pressure stage for microdiamond-bearing garnet–kyanite–gneisses have yet been found. The prolate shape of garnets developed during the earliest stages of exhumation that is recorded structurally by (L  S) tectonites, which subsequently accommodated progressive ductile SW shearing and folding up to shallow crustal levels. The majority of matrix kyanite and a later generation of garnet were formed during SW-directed shear under plane-strain conditions. Fluid inclusions entrapped in quartz during this stage of deformation underwent density loss and transformed to almost pure CO₂ inclusions by preferential loss of H₂O. Those inclusions armoured within garnet retained their primary 3-phase H₂O–CO₂ compositions. Reequilibration of fluid inclusions in quartz aggregates is most likely the result of recrystallization along with stress-induced, preferential H₂O leakage along dislocations and planar lattice defects which results in the predominance of CO₂ inclusions with supercritical densities. Carbonic fluid inclusions from adjacent kyanite–corundum-bearing pegmatoids and, the presence of shear-plane-parallel fluid inclusion planes within late quartz boudin structures consisting of pure CO₂-fluid inclusions with negative crystal shapes, bear witness of the latest stage of deformation by NE-directed extensional shear.This study shows that the textures of early fluid inclusions that formed already during the prograde metamorphic path can be preserved and used to derive information about the kinematics of subduction that is difficult to obtain from other sources. The textures of early inclusions, together with later generations of unaltered primary and secondary inclusions in metamorphic index minerals that can be linked to specific deformation stages and even P–T conditions, are a welcome supplement for the reconstruction of a rather detailed P–T–d path.  相似文献   

Research on fluid inclusions of the Yinshan polymetallic deposit, Jiangxi Province, China   总被引：1，自引：0，他引：1  

张德会  刘伟 《中国地球化学学报》1999,18(2):104-114

In this paper some new advances in the study of fluid inclusions of the Yinshan deposit in Jiangxi Province,China,are presented.The fluid inclusions of the deposit can be divided into four types:1) gas-rich inclusions;2)liquid-rich inclusions;3)salt-saturated H2O inclusions;and 4)single-phase or multiphase CO2-rich inclusions.Homogenization temperatures of the fluid inclusions range from 100 to 520℃,aminly in the range 120-400℃.The daughter crystal-bearing multiphase inclusions present in quartz porphyries(including Nos.13 and 4 dikes)have been observed.In ore veins,some daughter crystal-bearing multiphase inclusions have been observed.too.On the basis of the results of fluid inclusion research,the authors suggest that the ore-forming fluid must have a close genetic relation to magmatic hydrothermal solution.The ore-forming fluid was dominantly originated from the depth and the mixing of magmatic solution with meteoric water was enhanced during ascending of the fluid,accompanying immiscibility and boiling of fluid.Teher may be a conceales igneous body at the depth of the Yinshan deposity,which furnishes the scientific basis for metallogenic prognosis at th depth of the Yinshan deposit.  相似文献   

Fluid inclusions as microchemical systems: evidence and modelling of fluid–host interactions in plagioclase     

B. Kleinefeld  R. J. Bakker 《Journal of Metamorphic Geology》2002,20(9):845-858

Dense, CO₂‐rich fluid inclusions hosted by plagioclases, An₄₅ to An₅₄, of the O.‐v.‐Gruber‐ Anorthosite body, central Dronning Maud Land, East Antarctica, contain varying amounts of small calcite, paragonite and pyrophyllite crystals detected by Raman microspectroscopy. These crystals are reaction products that have formed during cooling of the host and the original CO₂‐rich H₂O‐bearing enclosed fluid. Variable amounts of these reaction products illustrates that the reaction did not take place uniformly in all fluid inclusions, possibly due to differences in kinetics as caused by differences in shape and size, or due to compositional variation in the originally trapped fluid. The reaction albite + 2anorthite + 2H₂O + 2CO₂ = pyrophyllite + paragonite + 2calcite was thermodynamically modelled with consideration of different original fluid compositions. Although free H₂O is not detectable in most fluid inclusions, the occurrence of OH‐bearing sheet silicates indicates that the original fluid was not pure CO₂, but contained significant amounts of H₂O. Compared to an actual fluid inclusion it is obvious, that volume estimations of solid phases can be used as a starting point to reverse the retrograde reaction and recalculate the compositional and volumetrical properties of the original fluid. Isochores for an unmodified inclusion can thus be reconstructed, leading to a more realistic estimation of P–T conditions during earlier metamorphic stages or fluid capturing.  相似文献   

Geochemical Evolution of Hydrothermal Fluids at the Daejang Cu–Zn–Pb Vein Deposit, Korea     

Sang Hoon CHOI 《Resource Geology》1998,48(3):171-182

Abstract: The Daejang mine is located within the Cretaceous Gyeongsang basin. Mineral paragenesis can be divided into four stages (stages I, II, III and IV) by major tectonic fracturing. Stages I, III and IV are economically barren. Stage II, at which the precipitation of major ore minerals occurred, is further divided into three substages with paragenetic time based on minor fractures and discernible mineral assemblages: substage IIa, marked by deposition of quartz and Fe–sulfides; substage IIb, by introduction of base-metal sulfides within carbonates and some quartz; substage IIc, by quartz and carbonates with various sulfosalts. Fluid inclusion data indicate a complex geochemical evolution of hydrothermal fluids. Both CO₂–rich and H₂O–rich fluids were trapped in fluid inclusions at stage I and substage IIa. It is suggested that a compositionally heterogeneous fluid was formed by fluid boiling and CO₂ immiscibility at temperatures of about 400° to 300°C. Composite lodes of base-metal sul–fides, carbonates and quartz at substage IIb were deposited in open spaces created by fracturing. The fracturing event prompted rapid decreases in pressure and temperature of residual fluids and resulted in retrograde fluid boiling at about 200 bars and 300°–250°C during substage IIb. The progressive loss of CO₂ by CO₂ effervescence and retrograde boiling from substage IIa and IIb fluids resulted in pH increase and related increase in carbonate activity, causing deposition of abundant carbonates. The change in pH also caused the decrease of stability of hydrogen sulfide with Cu, Zn and Pb chloride complexes (as main transporting agents at Daejang) and resulted in the pricipitation of base-metal minerals. Deposition of Ag– and Sb-bearing sul–fides and sulfosalts of substage IIc occurred at temperatures of about 250° to 150°C from a dominantly aqueous fluid with low salinity (down to 3. 0 equiv. wt % NaCl). At this substage, aqueous fluid formed by mixing with cooler and less saline meteoric groundwater. There is a systematic decrease in caculated δ¹⁸O_water values with the mineralization stage (and decreasing temperature) in the Daejang hydrothermal system, from values of about 11% for stage I, through about 4% for stages II and III, to about –3 per mil for stage IV. The result of stable isotope and fluid inclusion studies are interpreted to indicate progressive less evolved and/or unexchanged meteoric water influx of an early hydrothermal system formed by highly evolved meteoric waters.  相似文献   

Copper mineralization around the Ahar batholith, north of Ahar (NW Iran): Evidence for fluid evolution and the origin of the skarn ore deposit     

Habib Mollai  Rajesh Sharma  Georgia Pe-Piper 《Ore Geology Reviews》2009,35(3-4):401-414

This investigation presents and interprets fluid inclusion data from different lithological units of the Cu skarn deposits at Mazraeh, north of Ahar, Azarbaijan, NW Iran. The results provide an assessment of the P–T conditions and mineral–fluid evolution and suggest new exploration parameters. Five types of inclusions are recognized from quartz and garnet. The temperature of homogenization of Type I inclusions with daughter minerals halite and sylvite ranges from 312° to 470 °C with total salinity of 52 to 63 wt.% NaCl equiv.; Type II and III inclusions with halite have homogenization temperatures of 230° to 520 °C and salinity of 31 to 50 wt.% NaCl equiv. The salinity of Types IV and V biphase (liquid + vapor) inclusions, based on their final ice melting temperature, varies between 10.2 to 20.8 wt.% NaCl equiv. T_h vs. salinity plots of inclusions show that the salinity of the fluids correlates positively with temperature. The inclusions formed at low pressure. Changes in the temperature and salinity of the fluids can be reconstructed from the inclusions. Highly saline, high-temperature fluids were most abundant during the main chalcopyrite ore-forming phase in the skarn and mineralized quartz veins. Low-salinity aqueous fluids were abundant in barren veins, in which there is no evidence for early hot high-salinity brine, and might have resulted from late-stage dilution and mixing of hydrothermal fluids with meteoric water. Based on petrographic features and fluid-inclusion data, early-stage magnetite deposition is related to boiling of fluid at temperatures of about 500 °C. At a later stage, boiling at temperatures of around 320° to 400 °C favored the deposition of sulfides and Fe mobility was decreased at these lower temperatures. The following inclusion characteristics may be used as exploration parameters in the Mazraeh area. (i) Presence of high-temperature, salt-bearing inclusions, with T_h between 300 and 500 °C; (ii) High-salinity fluid inclusions; and (iii) Inclusions showing evidence of boiling of the fluid. In addition, the presence of magnetite is an important exploration parameter.  相似文献   

Synthetic fluid inclusions in natural quartz. III. Determination of phase equilibrium properties in the system H₂O-NaCl to 1000°C and 1500 bars     

R.J. Bodnar  C.W. Burnham  S.M. Sterner 《Geochimica et cosmochimica acta》1985,49(9):1861-1873

Phase equilibria in the system H₂O-NaCl have been determined to 1000°C and 1500 bars using synthetic fluid inclusions formed by healing fractures in inclusion-free Brazilian quartz in the presence of the two coexisting, immiscible H₂O-NaCl fluids at various temperatures and pressures. Petrographic and microthermometric analyses indicate that the inclusions trapped one or the other of the two fluids present, or mixtures of the two. Salinities of the two coexisting phases were obtained from heating and freezing studies on those inclusions which trapped only a single, homogeneous fluid phase.Results of the present study are consistent with previously published data on the H₂O-NaCl system at lower temperatures and pressures, and indicate that the two-phase field extends well into the P-T range of most shallow magmatic-hydrothermal activity. As a consequence, chloride brines exsolved from many epizonal plutons during the process of “second-boiling” should immediately separate into a high-salinity liquid phase and a lower salinity vapor phase and produce coexisting halite-bearing and vapor-rich fluid inclusions. This observation is consistent with results of numerous fluid inclusion studies of ore deposits associated with shallow intrusions, particularly the porphyry copper deposits, in which halite-bearing and coexisting vapor-rich inclusions are commonly associated with the earliest stages of magmatic-hydrothermal activity.  相似文献   

An experimental study of phase equilibria in the system H2O-CO2-NaCl at 800 °C and 9 kbar     

Kirill I. Shmulovich  Colin M. Graham 《Contributions to Mineralogy and Petrology》1999,136(3):247-257

Phase equilibria in the ternary system H₂O-CO₂-NaCl were studied at 800 °C and 9 kbar in internally heated gas pressure vessels using a modified synthetic fluid inclusion technique. The low rate of quartz overgrowth along the `b' and `a' axes of quartz crystals was used to avoid fluid inclusion formation during heating, prior to attainment of equilibrium run conditions. The density of CO₂ in the synthetic fluid inclusions was calibrated using inclusions in the binary H₂O-CO₂ system synthesised by the same method and measured on the same heating-freezing stage. In the two-phase field, two types of fluid inclusions with different densities of CO₂ were observed. Using mass balance calculations, these inclusions are used to constrain the miscibility gap and the orientation of two-phase tie-lines in the H₂O-CO₂-NaCl system at 800 °C and 9 kbar. The equation of state of Duan et al. (1995) approximately describes the P-T section of the ternary system up to about 40 wt% of NaCl. At higher NaCl concentrations the measured solubility of CO₂ in the brine is much smaller than predicted by the EOS. A “salting out” effect must be added to the equation of state to include coulomb interaction in the model of Anderko and Pitzer (1993) and Pitzer and Jiang (1996). The new experimental data together with published data up to 5 kbar (Shmulovich et al. 1995) encompass practically all subsolidus crustal P-T conditions. A feature of the new experimental results is the large compositional range in the H₂O-CO₂-NaCl system occupied by the stability fields of halite + CO₂-rich fluid ± H₂O-NaCl brine. The prediction of halite stability in equilibrium with CO₂-rich fluid in deep-crustal rocks is supported by recent petrological and fluid inclusion studies of granulites. Received: 29 June 1998 / Accepted: 17 March 1999  相似文献   

C–O–H–N fluids in quartz segregations from a major ductile shear zone: the Berzosa fault, Spanish Central System     

C. CASQUET 《Journal of Metamorphic Geology》1986,4(2):117-130

Abstract The Berzosa fault is a major ductile shear zone, the Berzosa Shear Zone (BSZ), which separates the ‘Ollo de Sapo’anticline from the inner higher-grade crystalline axis of the Iberian Hercynian Belt. This shear zone is the site of abundant early kinematic quartz (± Al-silicates) segregations, rich in fluid inclusions. Host rocks are medium-grade staurolite schists and sillimanite gneisses. Fluid inclusions in selected quartz segregations across the Berzosa shear zone have been studied by microthermometric methods as well as, in some instances, by Raman analysis. The recorded fluid inclusion history begins at the end of an intense secondary recrystallization period during late-peak metamorphic conditions and lasts until late in the uplift history of the zone. Three types of inclusions have been found, which in a time sequence are: CO₂± H₂O; H₂O+salt (B-type); and, N₂+CH₄. Three types of B inclusion may be distinguished in turn, depending on whether they were trapped during an earlier dynamic-recovery phase (B₁-type), formed later as intergranular trails (B₂-type), or were trapped apparently along with N₂+CH₄ in clusions from a heterogeneous fluid (B₃-type). Considerations from isochores confirm that CO₂± H₂O inclusions were trapped during late-peak and high-T retrograde metamorphic conditions (in the range 650–500°C and 5–2 kbar), whilst N₂+CH₄ inclusions, along with the B₃-type of inclusions, formed at low-pressures (<1 kbar) and temperatures (± 300°C). B₂-type inclusions were trapped chronologically between these two in a period in which strong inverse lateral thermal gradients developed in the zone. Inferred P-T paths for the area are convex to the T-axis.  相似文献   

Synthetic fluid inclusions XVIII: Experimental determination of the PVTX properties of H₂O-CH₄ to 500 °C, 3 kbar and X_CH4 ?4 mol.%     

Fang Lin 《Geochimica et cosmochimica acta》2010,74(11):3260-5902

The pressure-volume-temperature-composition (PVTX) properties of H₂O-CH₄ were determined from the bubble point curve to 500 °C and 3 kbar for compositions ?4 mol.% CH₄ using the synthetic fluid inclusion technique. H₂O-CH₄ inclusions were produced by loading known amounts of Al₃C₄ and H₂O into platinum capsules along with pre-fractured and inclusion-free quartz cores. During heating the Al₃C₄ and H₂O react to produce CH₄, and the H₂O-CH₄ homogeneous mixture was trapped as inclusions during fracture healing at elevated temperature and pressure. The composition of the fluid in the inclusion was confirmed using the weight loss technique after the experiment and by Raman spectroscopic analysis of the inclusions.Homogenization temperatures of the inclusions were determined and the results were used to construct iso-T_h lines, defined as a line connecting the formation temperature and pressure with the homogenization temperature and pressure. The pressure in the inclusion at the homogenization temperature was calculated from the Duan equation of state (EOS). The slope (ΔP/ΔT) of each iso-T_h line was calculated and the results fitted to a polynomial equation using step-wise multiple regression analysis to estimate the slope of the iso-T_h line as a function of the homogenization temperature and composition according to: