Three-dimensional Modeling of Ore-forming Elements and Mineralization Prognosis for the Yechangping Mo Deposit,Henan Province,China

Three-dimensional geochemical modeling of ore-forming elements is crucial for predicting deep mineralization.This approach provides key information for the quantitative prediction of deep mineral localization,three-dimensional fine interpolation,analysis of spatial distribution patterns,and extraction of quantitative mineral-seeking markers.The Yechangping molybdenum(Mo)deposit is a significant and extensive porphyry-skarn deposit in the East Qinling-Dabie Mo polymetallic metallogenic belt at the southern margin of the North China Block.Abundant borehole data on oreforming elements underpin deep geochemical predictions.The methodology includes the following steps:(1)Threedimensional geological modeling of the deposit was established.(2)Correlation,cluster,and factor analyses post delineation of mineralization stages and determination of mineral generation sequence to identify(Cu,Pb,Zn,Ag)and(Mo,W,mfe)assemblages.(3)A three-dimensional geochemical block model was constructed for Mo,W,mfe,Cu,Zn,Pb,and Ag using the ordinary kriging method,and the variational function was developed.(4)Spatial distribution and enrichment characteristics analysis of ore-forming elements are performed to extract geological information,employing the variogram and w(Cu+Pb+Zn+Ag)/w(Mo+W)as predictive indicators.(5)Identifying the western,northwestern,and southwestern areas of the mine with limited mineralization potential,contrasted by the northeastern and southeastern areas favorable for mineral exploration.

Unveil the Redox Evolution of Ore-forming Fluids using Sulfur Isotope:A Case Study of the Zhengguang Intermediate Sulfidation Epithermal Au-Zn Deposit,NE China

Oxygen fugacity(fO_(2))is a key intensity variable during the entire magmatic-hydrothermal mineralization courses.The redox state and its variations between different stages of the ore-forming fluids of intermediate sulfidation epithermal deposits are rarely deciphered due to the lack of appropriate approaches to determine fO_(2)of the fluids.Here,we reported theδ^(34)S of the sulfides from three different stages(stageⅠ,Ⅱ,Ⅲ)of Zhengguang,an Early Ordovician Au-rich intermediate sulfidation(IS)epithermal deposit,to decipher the redox evolution of the ore-forming fluids.The increasingδ^(34)S values from stageⅠpyrite(pyl,average-2.6‰)through py2(average-1.9‰)to py3(average-0.2‰)indicates a decrease of the oxygen fugacity of the ore-forming fluids.A compilation ofδ^(34)S values of sulfides from two subtypes of IS deposits(Au-rich and Ag-rich)from NE China shows that theδ^(34)S values of sulfides from Au-rich IS deposits are systematically lighter than those of Ag-rich IS Ag-Pb-Zn deposit,indicating the ore-forming fluids of the former are more oxidized than the latter.We highlight that sulfur isotopic composition of hypogene sulfides is an efficacious proxy to fingerprint the oxygen fugacity fluctuations of epithermal deposits and could potentially be used to distinguish the subtypes of IS deposits.

Metallogenic Age and Ore-forming Material Sources of the Dahongshan Fe-Cu Deposit,Yunnan Province:Insights from Molybdenite Re-Os Dating and H-O-S-Pb Isotopes

The Dahongshan Fe-Cu(-Au)deposit is a superlarge deposit in the Kangdian metallogenic belt,southwestern China,comprising approximately 458 Mt of Fe ores(40%Fe)and 1.35 Mt Cu.Two main types of Fe-Cu(-Au)mineralization are present in the Dahongshan deposit:(1)early submarine volcanic exhalation and sedimentary mineralization characterized by strata-bound fine-grained magnetite and banded Fe-Cu sulfide(pyrite and chalcopyrite)hosted in the Na-rich metavolcanic rocks;(2)late hydrothermal(-vein)type mineralization characterized by Fe-Cu sulfide veins in the hosted strata or massive coarse-grained magnetite orebodies controlled by faults.While previous studies have focused primarily on the early submarine volcanic and sedimentary mineralization of the deposit,data related to late hydrothermal mineralization is lacking.In order to establish the metallogenic age and ore-forming material source of the late hydrothermal(-vein)type mineralization,this paper reports the Re-Os dating of molybdenite from the late hydrothermal vein Fe-Cu orebody and H,O,S,and Pb isotopic compositions of the hydrothermal quartz-sulfide veins.The primary aim of this study was to establish the metallogenic age and ore-forming material source of the hydrothermal type orebody.Results show that the molybdenite separated from quartz-sulfide veins has a Re-Os isochron age of 831±11 Ma,indicating that the Dahongshan Fe-Cu deposit experienced hydrothermal superimposed mineralization in Neoproterozoic.The molybdenite has a Re concentration of 99.7-382.4 ppm,indicating that the Re of the hydrothermal vein ores were primarily derived from the mantle.The δ^(34)S values of sulfides from the hydrothermal ores are 2‰-8‰ showing multi-peak tower distribution,suggesting that S in the ore-forming period was primarily derived from magma and partially from calcareous sedimentary rock.Furthermore,the abundance of radioactive Pb increased significantly from ore-bearing strata to layered and hydrothermal vein ores,which may be related to the later hydrothermal transformation.The composition of H and O isotopes within the hydrothermal quartz indicates that the ore-forming fluid is a mixture of magmatic water and a small quantity of water.These results further indicate that the late hydrothermal orebodies were formed by the Neoproterozoic magmatic hydrothermal event,which might be related to the breakup of the Rodinia supercontinent.Mantle derived magmatic hydrothermal fluid extracted ore-forming materials from the metavolcanic rocks of Dahongshan Group and formed the hydrothermal(-vein)type Fe-Cu orebodies by filling and metasomatism.

In, Sn, Pb and Zn Contents and Their Relationships in Ore-forming Fluids from Some In-rich and In-poor Deposits in China

All the indium-rich deposits with indium contents in ores more than 100×10^-6 seems to be of cassiterite-sulfide deposits or Sn-bearing Pb-Zn deposits, e.g., in the Dachang Sn deposit in Guangxi, the Dulong Sn-Zn deposit in Yunnan, and the Meng＇entaolegai Ag-Pb-Zn deposit in Inner Mongolia, the indium contents in ores range from 98×10^-6 to 236×10^-6 and show a good positive correlation with contents of zinc and tin, and their correlation coefficients are 0.8781 and 0.7430, respectively. The indium contents from such Sn-poor deposits as the Fozichong Pb-Zn deposit in Guangxi and the Huanren Pb-Zn deposit in Liaoning are generally lower than 10×10^-6, i.e., whether tin is present or not in a deposit implies the enrichment extent of indium in ores. Whether the In enrichment itself in the ore -forming fluids or the ore-forming conditions has actually caused the enrichment/depletion of indium in the deposits？ After studying the fluid inclusions in quartz crystallized at the main stage of mineralization of several In-rich and In-poor deposits in China, this paper analyzed the contents and studied the variation trend of In, Sn, Pb and Zn in the ore-forming fluids. The results show that the contents of lead and zinc in the ore-forming fluids of In-rich and -poor deposits are at the same level, and the lead contents range from 22×10^-6 to 81×10^-6 and zinc from 164×10^-6 to 309×10^-6, while the contents of indium and tin in the ore-forming fluids of In-rich deposits are far higher than those of Inpoor deposits, with a difference of 1-2 orders of magnitude. Indium and tin contents in ore-forming fluid of In-rich deposits are 1.9×10^-6-4.1×10^-6 and 7×10^-6-55×10^-6, and there is a very good positive correlation between the two elements, with a correlation coefficient of 0.9552. Indium and tin contents in ore-forming fluid of In-poor deposits are 0.03×10^-6-0.09×10^-6 and 0.4×10^-6-2.0×10^-6, respectively, and there is no apparent correlation between them. This indicates, on one hand, that In-rich oreforming fluids are the material basis for the formation of In-rich deposits, and, on the other hand, tin probably played a very important role in the transport and enrichment of indium.

Rare Earth Elements Geochemistry of Laowan Gold Deposit in Henan Province: Trace to Source of Ore-Forming Materials

The compositions of REE in quartz and pyrite from the main stage of the Laowan gold deposit in Henan Province and that in quartz from Laowan granite were determined by inductively coupled plasma-mass-spectrometry （ICP-MS） to trace the source of ore-forming materials. Meanwhile, the REE compositions of the deposit ore, granite and metamorphic wall rock were also considered for comparative studies in detail. The range of ∑REE of quartz and pyrite from the deposit ores is 4.18 × 10^-6- 30.91 × 10^-6, the average of ∑REE is 13.39 × 10^-6, and the average of ∑REE of quartz in the Laowan granite is 6.68 × 10^-6. There is no distinct difference of REE parameters between the deposit ore quartz and granite quartz. The quartz in gold deposit has the same REE particular parameters as quartzes from Laowan granite, such as δEu, δCe, （La/Yb）N and （La/Sm）N, partition degree of LREE to HREE, especially, the chondrite-normalized REE patterns, but no similarity to those from metamorphic wall rock, which shows that ore-forming hydrothermal fluid is mainly the fluid coming from the Laowan granite magma, rather than metamorphic fluid. Meanwhile, comparison studies on REE features between minerals from the deposit ores and related geological bodies in the deposit show that REE characteristics of minerals can serve as an indicator of ore-forming fluid properties and sources, while the REE characteristics of the bulk samples （such as deposit ores, granites and wall rocks） can not trace the source of the ore-forming materials exactly.

REE Geochemistry of Sulfides from the Huize Zn-Pb Ore Field, Yunnan Province: Implication for the Sources of Ore-forming Metals

REE abundances in sulfides from the Huize Zn-Pb ore field were determined with the ICPMS after preconcentration. The REE abundances in 26 sulfide samples （including pyrite, galena and sphalerite） are very low, with the ~REE ranging from 1.6×10^-9 to 166.8×10^-9. Their LREE/HREE ratios range from 7.6 to 98, showing LREE enrichment relatively. The JEu values are below 1, indicating that they were deposited from an Eu-depleted and reducing fluid-system. Similar to the ore-hosting carbonate strata, calcite separates from carbonate veinlets filling in the fractures or faults crosscutting the carbonate strata also show clear Eu-depletion. This indicates that the carbonate veinlets and their parent fluid was possibly sourced from the strata and inherited the REE geochemical features of the strata. Therefore, REE-geochemical characteristics of both the sulfides and calcites, which were deposited from an ore-forming hydrothermal system, are similar to those of carbonate strata, and strongly suggest that the ore metals were mainly sourced from carbonate strata.

Numerical Modelling of Ore-forming Dynamics of Fractal Dispersive Fluid Systems

Based on an analysis of the fractal structures and mass transport mechanism of typical shear-fluid-ore formation system, the fractal dispersion theory of the fluid system was used in the dynamic study of the ore formation system. The model of point-source diffusive illuviation of the shear-fluid-ore formation system was constructed, and the numerical simulation of dynamics of the ore formation system was finished. The result shows that: (1) The metallogenic system have nested fractal structure. Different fractal dimension values in different systems show unbalance and inhomogeneity of ore-forming processes in the geohistory. It is an important parameter to symbolize the process of remobilization and accumulation of ore-forming materials. Also it can indicate the dynamics of the metallogenic system quantitatively to some extent. (2) In essence, the fractal dispersive ore-forming dynamics is a combination of multi-processes dominated by fluid dynamics and supplemented by molecule dispersion in fluids and fluid-rock interaction. It changes components and physico-chemical properties of primary rocks and fluids, favouring deposition and mineralization of ore-forming materials. (3) Gold ore-forming processes in different types of shear zones are quite different. (1) In a metallogenic system with inhomogeneous volumetric change and inhomogeneous shear, mineralization occurs in structural barriers in the centre of a shear zone and in geochemical barriers in the shear zone near its boundaries. But there is little possibility of mineralization out of the shear zone. (2) As to a metallogenic system with inhomogeneous volumetric change and simple shear, mineralization may occur only in structural barriers near the centre of the shear zone. (3) In a metallogenic system with homogeneous volumetric change and inhomogeneous shear, mineralization may occur in geochemical barriers both within and out of the shear zone.

Geochemical Characteristics and Sources of Ore-forming Fluids of the Mayuan Pb-Zn Deposit,Nanzheng,Shaanxi,China

The Mayuan stratabound Pb-Zn deposit in Nanzheng,Shaanxi Province,is located in the northern margin of the Yangtze Plate,in the southern margin of the Beiba Arch.The orebodies are stratiform and hosted in breciated dolostone of the Sinian Dengying Formation.The ore minerals are primarily sphalerite and galena,and the gangue minerals comprise of dolomite,quartz,barite,calcite and solid bitumen.Fluid inclusions from ore-stage quartz and calcite have homogenization tempreatures from 98 to 337℃ and salinities from 7.7 wt%to 22.2 wt%（NaCl equiv.）.The vapor phase of the inclusions is mainly composed of CH_4 with minor CO_2 and H_2S.The δD_（fluid） values of fluid inclusions in quartz and calcite display a range from-68‰ to-113‰（SMOW）,and the δ^（18）O_（fluid）values calculated from δ^（18）O_（quartz） and δ^（18）O_（calcite） values range from 4.5‰ to 16.7‰（SMOW）.These data suggest that the ore-forming fluids may have been derived from evaporitic sea water that had reacted with organic matter.The δ^（13）C_（CH4） values of CH_4 in fluid inclusions range from-37.2‰ to-21.0‰（PDB）,suggesting that the CH_4 in the ore-forming fluids was mainly derived from organic matter.This,together with the abundance of solid bitumen in the ores,suggest that organic matter played an important role in mineralization,and that the thermochemical sulfate reduction（TSR） was the main mechanism of sulfide precipitation.The Mayuan Pb-Zn deposit is a carbonate-hosted epigenetic deposit that may be classified as a Mississippi Valley type（MVT） deposit.

REE Geochemistry of Fluorite from the Maoniuping REE Deposit,Sichuan Province,China:Implications for the Source of Ore-forming Fluids

Fluorite is one of the main gangue minerals in the Maoniuping REE deposit, Sichuan Province, China. Fluorite with different colors occurs not only within various orebodies, but also in wallrocks of the orefield. Based on REE geochemistry, fluorite in the orefleld can be classified as the LREE-rich, LREE-flat and LREE-depleted types. The three types of fluorite formed at different stages from the same hydrothermal fluid source, with the LREE-rich fluorite forming at the relatively early stage, the LREE-flat fluorite in the middle, and the LREE-depleted fluorite at the latest stage. Various lines of evidence demonstrate that the variation of the REE contents of fluorite shows no relation to the color. The mineralization of the Maouiuping REE deposit is associated spatially and temporally with carbonatite-syenite magmatism and the ore-forming fluids are mainly derived from carbonatite and syenite melts.

Ore-forming Fluid Systems and Mineralization in the Eastern Jiangnan Uplift in the Border Area of Anhui and Jiangxi Provinces, China

Obvious differences in mineralization characteristics exist between the southern and northern parts of the eastern part of the Jiangnan Uplift in northern Jiangxi Province and southern Anhui Province. The regional metallogeny is discussed, and the ore-forming fluid systems are classified in this article. It is proposed that the fluid ore-forming activities in the Jiangnan Uplift both in northern Jiangxi and southern Anhui have close relationships with the crust-mantle interaction and magmatic-tectonic activities. The types and scales of the mineralization on the both sides of the eastern Jiangnan Uplift were determined by fluid ore-forming systems and geological backgrounds.

Characteristics of Pegmatite-Related Fluids and Significance to Ore-Forming Processes in the Zhaxikang Pb-Zn-Sb Polymetallic Deposit,Tibet,China

The Zhaxikang Pb-Zn-Sb polymetallic deposit is one of the most important deposits in the newly recognized southern Tibet antimony-gold metallogenic belt.Compared to the porphyry deposits in the Gangdese belt,much less researches have addressed these deposits,and the genesis of the Zhaxikang deposit is still controversial.Based on field investigation,petrographic,microthermometric,Laser Raman Microprobe（LRM） and SEM/EDS analyses of fluid,melt-fluid,melt and solid inclusions in quartz and beryl from pegmatite,this paper documents the characteristics and the evolution of primary magmatic fluid which was genetically related to greisenization,pegmatitization,and silification in the area.The results show that the primary magmatic fluids were derived from unmixing between melt and fluid and underwent a phase separation process soon after the exsolution.The primary magmatic fluids are of low salinity,high temperature,and can be approximated by the H_2O-NaCl-CO_2 system.The presence of Mn-Fe carbonate in melt-fluid inclusions and a Zn-bearing mineral（gahnite） trapped in beryl and in inclusions from pegmatite indicates high Mn,Fe,and Zn concentrations in the parent magma and magmatic fluids,and implies a genetic link between pegmatite and Pb-Zn-Sb mineralization.High B and F concentrations in the parent magma largely lower the solidus of the magma and lead to late fluid exsolution,thus the primary magmatic fluids related to pegmatite have much lower temperature than those in most porphyry systems.Boiling of the primary magmatic fluids leads to high-salinity and high-temperature fluids which have high capacity to transport Pb,Zn and Sb.The decrease in temperature and mixing with fluids from other sources may have caused the precipitation of Pb-Zn-Sn（Au） minerals in the distal fault systems surrounding the causative intrusion.

Discriminating characters of ore-forming intrusions in the super-large Chalukou porphyry Mo deposit,NE China

The Chalukou porphyry Mo deposit, located in the Great Hinggan Range, is the largest Mo deposit in northeast China, although the age and genesis of the associated magmatic intrusions remain debated.Here we report zircon U-Pb ages and trace elements, whole rock geochemistry and Sre Nd isotope data with a view to understand the relationship between the magmatism and molybdenum mineralization.Zircon U-Pb analysis yield an age of 475 Ma for rhyolite in the older strata, 168 Ma for the premineralization monzogranite, and 154 Ma for the syn-mineralization granite porphyry. The granite porphyry and quartz porphyry are considered as the ore-forming intrusions. These rocks are peraluminous, alkali-calcic, and belong to high-K to shoshonitic series with a strong depletion of Eu. They also display characteristics of I-type granites. The rocks exhibit wide variations of(87 Sr/86 Sr)iin the range of 0.705426 -0.707363, and ε_(Nd)(t) of -3.7 to 0.93. Zircon REE distribution patterns show characteristics between crust and the mantle, implying magma genesis through crust-mantle interaction. The Fe_2O_3/FeO values(average 1) for the whole rock and EuN/Eu*Nvalues(average 0.45), Ce^(4+)/Ce^(3+) values(average 301)for zircon grains from the granite porphyry are higher than those from other lithologies. These features suggest that the ore-forming intrusions(syn-mineralization porphyry) had higher oxygen fugacity conditions than those of the pre-mineralization and post-mineralization rocks. The Chalukou Mo deposit formed in relation to the southward subduction of the Mongol-Okhotsk Ocean. Our study suggests that the subduction-related setting, crust-mantle interaction, and the large-scale magmatic intrusion were favorable factors to generate the super-large Mo deposits in this area.

Experimental Observation of the Ore-Forming Fluid NaCl-H_2O System in the Earth Interior

The NaCl-H_2O binary system is a major component of solutions coexisting with ores. Observation ofsaturated solutions of NaCl-H_2O by using the method of hydrothermal diamond anvil cell (HDAC) is a new approach tothe study of ore-forming fluids. The salinities of NaCl-H_2O solutions in experimental observation are in a range of 32-55%. The observed temperature range is 25℃-850℃, and the pressure range 1 atm-10 kb. In this temperature-pressure range, the supercritical single phase, two phases (L,V) close to the critical state and two-phased (L+V) immis-cible region were observed. And for the salinity of 35% the two phase L+V immiscible region of NaCl-H_2O solutionwas observed in a range of 253-720℃. Another temperature range, 400-817℃, was observed for the immiscible two-phased region of 50% salinity solution. In the high-temperature part of the two-phased immiscible region, the phase na-ture is very unstable. A "critical phenomenon" was observed when the heating path was very close to the critical state.It is possible to observe a 'critical phenomenon': an "explosion" occurred almost constantly at the interface between theliquid and vapour and the interface is rather obscure. A continuous transition between phases L and V could be foundin the immiscible L+V phase while heating continuously. Moreover, as the NaCl-H_2O solution was separated into liq-uid and vapour phases, static charges surrounding each vapour bubble could be seen, and these bubbles were attractedtogether by the static charges to form a special solution structure. Besides, critical states of different salinities of NaCl-H_2O were observed in order to study the properties of the fluids occurring in the rocks in the earth interior, the origin ofore-bearing fluids and the significance of supercritical fluid with respect to the ore formation. The comparison of the sa-linity data of the fluid inclusions in the minerals of ore deposits with observations of NaCl-H_2O under HDAC in theconditions of high temperatures and pressures, combined with further thermodynamic analysis of ore-formation condi-tions would explain in depth the factors determining the ore formation.

Fluid Evolution and Ore-forming Processes of the Jiama Cu Deposit, Tibet： Evidence from Fluid Inclusions

The Jiama deposit is a large copper deposit in Tibet. Mineralization occurs in three different host rocks： skarn, hornfels and porphyry. A detailed fluid inclusion study was conducted for veins in the different host rocks to investigate the relationship between fluid evolution and ore-forming processes. Based on examination of cores from 36 drill holes, three types of veins （A, B and D） were identified in the porphyries, four types （I, II, III and IV） in the skarn, and three （a, b and c） in the hornfels. The crosscutting relationships of the veins and that of the host rocks suggest two hydrothermal stages, one early and one late stage. Fluid inclusions indicate that the Jiama hydrothermal fluid system underwent at least two episodes of fluid boiling. The first boiling event occurred during the early hydrothermal stage, as recorded by fluid inclusions hosted in type A veins in the porphyries, type a veins in the hornfels, and wollastonite in the skarns. This fluid boiling event was associated with relatively weak mineralization. The second boiling event occurred in the late hydrothermal stage, as determined from fluid inclusions hosted in type B and D veins in the porphyries, type I to IV veins in the skarns, and type b and c veins in the hornfels. This late boiling event, together with mixing with meteoric water, was responsible for more than 90% of the metal accumulation in the deposit. The first boiling only occurred in the central part of the deposit and the second boiling event took place across an entire interlayered structural zone between hornfels and marble. A spatial zoning of ore-elements is evident, and appears to be related to different migration pathways and precipitation temperatures of Cu, Mo, Pb, Zn, Au and Ag.

Ore-forming Conditions and Prospecting in the West Kunlun Area,Xinjiang, China

The West Kunlun ore-forming belt is located between the northwestern Qinghai-Tibet Plateau and southwestern Tarim Basin. It situated between the Paleo-Asian Tectonic Domain and Tethyan Tectonic Domain. It is an important component of the giant tectonic belt in central China (the Kunlun-Qilian-Qinling Tectonic Belt or the Central Orogenic Belt). Many known ore-forming belts such as the Kunlun-Qilian Qinling ore-forming zone, Sanjiang (or Three river) ore-forming zone, Central Asian ore-forming zone, etc. pass through the West Kunlun area. Three ore-forming zones and seven ore-forming subzones were classified, and eighteen mineralization areas were marked. It is indicated that the West Kunlun area is one of the most favorable region for finding out large and superlarge ore deposits.

Ore-forming Fluid Characteristics of the Saishitang Cu-polymetallic Deposit in Qinghai Province,China

Saishitang Cu-polymetallic deposit is located in the southeast section of Late Paleozoic arcfoid in the southeastern margin of Qaidam platform. Accoring to the geological process of the deposit, four mineralization episodes were identified： melt/fluid coexisting period （O）, skarn period （A）, first sulfide period （B） and second sulfide period （C）, and 10 stages were finally subdivided. Three types of inclusions were classified in seven stages, namely crystal bearing inclusions （type I）, aqueous inclusions （type Ⅱ） and pure liquid inclusions （type Ⅲ）. Type I and Ⅱ inclusions were observed in stage O1, having homogenization temperature from 252 to 431℃, and salinities ranging from 24.3% to 48.0%. Type I inclusion was present in stage A1, having homogenization temperature from 506 to 548℃, and salinities ranging from 39.4% to 44.6%. In stage B1, type Ⅱ and Ⅲ inclusions were observed, with homogenization temperature concentrating between 300-400℃, and salinities from 0.4% to 4.3%. Type II inclusions were present in stage B2, with homogenization temperature varying from 403 to 550℃. In stage C1, type I and II inclusion commonly coexisted, and constituted a boiling inclusion group, having homogenization temperatures at 187-463℃, and salinities in a range of 29.4%-46.8% and 2.2%-11.0%. Type II and III inclusions were developed in stage C2, having homogenization temperature at 124-350℃, and salinities ranging between 1.6% and 15.4%. In stage C3, type Ⅱ and Ⅲ inclusions were presented, with a homogenization temperature range of 164-360℃, and salinities varying from 4.0% to 11.0%. The results of micro-thermal analysis show that fluids are characterized by high temperature and high salinity in stage O1 and A1, and experienced slight decrease in temperature and dramatic decrease in salinity in stage B1 and B2. In stage C1, the salinity of fluid increased greatly and a further decrease of temperature and salinity occurred in stage C2 and C3. Fluids boiled in stage C1. With calculated pressure of 22 MPa from the trapping temperature of 284- 289℃, a mineralization depth of 2.2 km was inferred. Results of Laser Raman Spectroscopy show high density of H2_O, CH_4 and CO_2 were found as gas composition. H-O isotope study indicates the ore- forming fluids were the mixture of magmatic water and meteoric water. Physicochemical parameters of fluids show oxygen and sulfur fugacity experienced a decrease, and redox state is weakly reducing. Along with fluid evolution, oxidation has increased slightly. Comprehensive analysis shows that melt exsolution occurred during the formation of quartz diorite and that metal elements existed and migrated in the form of chlorine complex. Immiscible fluid separation and boiling widely occurred after addition of new fluids, bringing about dissociation of chlorine-complex, resulting in a great deal of copper precipitation. In conclusion, Saishitang deposit, controlled by regional tectonics, is formed by metasomatism between highly fractionated mineralization rock body and wall rock, and belongs to banded skarn Cu-polymetallic deposit.Abstract： Saishitang Cu-polymetallic deposit is located in the southeast section of Late Paleozoic arcfoid in the southeastern margin of Qaidam platform. Accoring to the geological process of the deposit, four mineralization episodes were identified： melt/fluid coexisting period （O）, skarn period （A）, first sulfide period （B） and second sulfide period （C）, and 10 stages were finally subdivided. Three types of inclusions were classified in seven stages, namely crystal bearing inclusions （type I）, aqueous inclusions （type Ⅱ） and pure liquid inclusions （type Ⅲ）. Type I and II inclusions were observed in stage O1, having homogenization temperature from 252 to 431℃, and salinities ranging from 24.3% to 48.0%. Type I inclusion was present in stage A1, having homogenization temperature from 506 to 548℃, and salinities ranging from 39.4% to 44.6%. In stage B1, type II and III inclusions were observed, with homogenization temperature concentrating between 300-400℃, and salinities from 0.4% to 4.3%. Type II inclusions were present in stage B2, with homogenization temperature varying from 403 to 550℃. In stage C1, type I and II inclusion commonly coexisted, and constituted a boiling inclusion group, having homogenization temperatures at 187-463℃, and salinities in a range of 29.4%-46.8% and 2.2%-11.0%. Type II and III inclusions were developed in stage C2, having homogenization temperature at 124-350℃, and salinities ranging between 1.6% and 15.4%. In stage C3, type II and Ⅲ inclusions were presented, with a homogenization temperature range of 164-360℃, and salinities varying from 4.0% to 11.0%. The results of micro-thermal analysis show that fluids are characterized by high temperature and high salinity in stage O1 and A1, and experienced slight decrease in temperature and dramatic decrease in salinity in stage B1 and B2. In stage C1, the salinity of fluid increased greatly and a further decrease of temperature and salinity occurred in stage C2 and C3. Fluids boiled in stage C1. With calculated pressure of 22 MPa from the trapping temperature of 284- 289℃, a mineralization depth of 2.2 km was inferred. Results of Laser Raman Spectroscopy show high density of H_2O, CH_4 and CO_2 were found as gas composition. H-O isotope study indicates the ore- forming fluids were the mixture of magmatic water and meteoric water. Physicochemical parameters of fluids show oxygen and sulfur fugacity experienced a decrease, and redox state is weakly reducing. Along with fluid evolution, oxidation has increased slightly. Comprehensive analysis shows that melt exsolution occurred during the formation of quartz diorite and that metal elements existed and migrated in the form of chlorine complex. Immiscible fluid separation and boiling widely occurred after addition of new fluids, bringing about dissociation of chlorine-complex, resulting in a great deal of copper precipitation. In conclusion, Saishitang deposit, controlled by regional tectonics, is formed by metasomatism between highly fractionated mineralization rock body and wall rock, and belongs to banded skarn Cu-polymetallic deposit.

A Study on the Ore-forming Effect of Mantle-derived Fluid

Based on summarizing of the effect of mantle-derived fluid on the formation of ores, especially on gold ore, and with the latest investigations, such as the formation of ore from the action of shallow-deep fluid, the transportation effect of the thermal energy by mantle-derived fluid, this paper mainly aims at the effect of mantle-derived fluid on the generation of hydrocarbons. With the proof from geochemistry and fluid inclusion, it was suggested that the mantle-derived fluid not only supplied source materials for hydrocarbons, but also supplied essential energy and matter necessary for the generation of hydrocarbons. The mantle-derived fluid had a good effect, but at the same time it had an adverse effect under specific conditions, on the formation of reservoirs. This paper also discusses the future direction and significance of studying mantle-derived fluid.

Ore-forming Fluid and Mineral Source of the Hongshi Copper Deposit in the Kalatage Area, East Tianshan, Xinjiang, NW China

The Hongshi copper deposit is located in the middle of the Kalatage ore district in the northern segment of the Dananhu-Tousuquan island-arc belt in East Tianshan, Xinjiang, NW China. This study analyses the fluid inclusions and H, O, and S stable isotopic compositions of the deposit. The fluid-inclusion data indicate that aqueous fluid inclusions were trapped in chalcopyrite-bearing quartz veins in the gangue minerals. The homogenization temperatures range from 108°C to 299°C, and the salinities range from 0.5% to 11.8%, indicating medium to low temperatures and salinities. The trapping pressures range from 34.5 MPa to 56.8 MPa. The δ^（18）O_（H_2O） values and δD values of the fluid range from -6.94‰ to -5.33‰ and from -95.31‰ to -48.20‰, respectively. The H and O isotopic data indicate that the ore-forming fluid derived from a mix of magmatic water and meteoric water and that meteoric water played a significant role. The S isotopic composition of pyrite ranges from 1.9‰ to 5.2‰, with an average value of 3.1‰, and the S isotopic composition of chalcopyrite ranges from -0.9‰ to 4‰, with an average value of 1.36‰, implying that the S in the ore-forming materials was derived from the mantle. The introduction of meteoric water decreased the temperature, volatile content, and pressure, resulting in immiscibility. These factors may have been the major causes of the mineralization of the Hongshi copper deposit. Based on all the geologic and fluid characteristics, we conclude that the Hongshi copper deposit is an epithermal deposit.

Rb-Sr Dating of Pyrite and Quartz Fluid Inclusions and Origin of Ore-forming Materials of the Jinshan Gold Deposit, Northeast Jiangxi Province, South China

The Jinshan gold deposit is located in the Northeast Jiangxi province,South China,which related to the ductile shear zone.It contains two ore types,i.e.the alteration-type ore and the goldbearing quartz vein ore.Rb-Sr age dating is applied to both gold-bearing pyrite in the alteration-type ore and fluid inclusion in the gold-bearing quartz vein to make clear the time of the gold mineralization of the Jinshan deposit.Analytical results of this study yielded that the age of the alteration-type ore bodies is about 838±110Ma,with an initial 87Sr/86Sr value of 0.7045±0.0020.However,the age of the gold-bearing quartz vein-type ore is about 379±49Ma,and the initial 87Sr/86Sr is 0.7138±0.0011.Based on the age data from this work and many previous studies,the authors consider that the Jinshan gold deposit is a product of multi-staged mineralization,which may include the Jinninian,Caledonian,Hercynian,and Yanshanian Periods.Among them,the Jinninian Period and the Hercynian Period might be the two most important ore-forming periods for Jinshan deposit.The Jinninian Period is the main stage for the formation of alteration-type ore bodies,while the Hercynian Period is the major time for ore bodies of gold-bearing quartz vein type.The initial values of the 87Sr/86Sr from this study,as well as the previous isotope and trace element studies,indicate that the ore-forming materials mainly derived from the metamorphic wall rocks,and the ore-forming fluids mainly originated from the deep metamorphic water.

Ore-Forming Mechanism of the Asikaerte Granitic Pegmagtite Beryllium Deposit in Xinjiang, China

Objective Granitic pegmatite has great significance for studying magmatic-hydrothermal evolution, which is the main formation mechanism of rare metal deposits. Conventionally, granitic pegmatite rare metal deposits are regarded as crystallization from H20-saturated granite magma that formed in the late fractional crystallization of granitic magma. However, some scholars recently believed that the liquid immiscibility of granitic magma promoted the formation of pegmatite deposits. The Asikaerte beryllium deposit in Xinjiang, China, bearing metallogenic belts from lower granite belt to upper pegmatite belt, could benefit us to understand the formation of pegmatite through analyzing fluid and melt inclusions data.