Trace-element compositions of single fluid inclusions in the Kofu granite, Japan: Implications for compositions of granite-derived fluids

Fluid inclusions in quartz from miarolitic cavities, pegmatites, and quartz veins in Miocene biotite-granite plutons, Kofu, Japan, were analyzed by particle-induced X-ray emission to examine chemistries and behaviors of granite-derived fluids in island-arc granite. Most inclusions are aqueous two-phase inclusions, and halite-bearing polyphase inclusions are also observed in quartz veins in the upper part of the plutons. From element contents of fluid inclusions in the miarolitic cavities, the original fluid released from the granite plutons during solidification is inferred to have concentrations of Mn, Fe, Cu, Zn, Ge, Br, Rb, Pb, and Ba of several tens to hundreds of parts per million by weight (ppm) and a salinity of about 10 wt% NaCl equivalent. We estimated the formation conditions of the fluid to have been at about 1.3–1.9 kb and 530–600°C on the basis of the homogenization temperatures of the inclusions and the solidification conditions of the plutons. The polyphase inclusions probably originated from hypersaline fluid by boiling of part of the released fluid during its ascent in the plutons. The polyphase inclusions contain several hundreds to tens of thousands of ppm of Fe and Mn, and tens to several hundreds of ppm of Cu, Zn, Br, Rb, and Pb. The salinities are about 35 wt% NaCl equivalent. Compositional variations in two-phase inclusions from the miarolitic cavities and quartz veins are primarily explained by mineral precipitation with dilution by surface water exerting a secondary influence. Thus, chemistries and behaviors of the granite-derived fluids in the plutons can be explained by mineral precipitation, boiling, and dilution of the originally released fluid.     

Fluid inclusion from drill hole DW-5, Hohi geothermal area, Japan: Evidence of boiling and procedure for estimating CO2 content

Fluid inclusion studies have been used to derive a model for fluid evolution in the Hohi geothermal area, Japan. Six types of fluid inclusions are found in quartz obtained from the drill core of DW-5 hole. They are: (I) primary liquid-rich with evidence of boiling; (II) primary liquid-rich without evidence of boiling; (III) primary vapor-rich (assumed to have been formed by boiling); (IV) secondary liquid-rich with evidence of boiling; (V) secondary liquid-rich without evidence of boiling; (VI) secondary vapor-rich (assumed to have been formed by boiling). Homogenization temperatures (T_h) range between 196 and 347°C and the final melting point of ice (T_m) between −0.2 and −4.3°C. The CO₂ content was estimated semiquantitatively to be between 0 and 0.39 wt. % based on the bubble behavior on crushing. NaCl equivalent solid solute salinity of fluid inclusions was determined as being between 0 and 6.8 wt. % after minor correction for CO₂ content.Fluid inclusions in quartz provide a record of geothermal activity of early boiling and later cooling. The CO₂ contents and homogenization temperatures of fluid inclusions with evidence of boiling generally increase with depth; these changes, and NaCl equivalent solid solute salinity of the fluid can be explained by an adiabatic boiling model for a CO₂-bearing low-salinity fluid. Some high-salinity inclusions without CO₂ are presumed to have formed by a local boiling process due to a temperature increase or a pressure decrease. The liquid-rich primary and secondary inclusions without evidence of boiling formed during the cooling process. The salinity and CO₂ content of these inclusions are lower than those in the boiling fluid at the early stage, probably as a result of admixture with groundwater.     

Ore-forming fluid and mineralization of Caijiaying and Dajing polymetallic ore deposits

Fluid inclusions from the Dajing and Caijiaying deposits have nearly the same ho-mogenization temperature. Correlation between temperature and salinity shows that both Sn-and Cu-bearing fluids Sn and Cu were present in the Dajing deposit but only one kind of fluids continuously evolved in the Caijiaying deposit. Study on rare earth elements (REE) in ancient fluid from the inclusions indicates that the fluid of Sn mineralizing stage in Dajing was derived from remelting magma of the continental crust, and the fluid of Cu-Pb-Zn mineralizing stage in the Dajing deposit and the fluid of Cu-Pb-Zn mineralization in the Caijiaying deposit were derived from the mantle. It is concluded that the Cu-Pb-Zn mineralizations in the Dajing and Caijiaying deposits resulted from the identical tectono-thermal event of magma-fluids induced by Mesozoic tectonic transition and extension in the eastern part of North China Craton.     

Geological and geochemical characteristics of the Baogudi Carlintype gold district(Southwest Guizhou,China) and their geological implications

The newly discovered Baogudi gold district is located in the southwestern Guizhou Province,China,where there are numerous Carlin-type gold deposits.To better understand the geological and geochemical characteristics of the Baogudi gold district,we carried out petrographic observations,elemental analyses,and fluid inclusion and isotopic composition studies.We also compared the results with those of typical Carlin-type gold deposits in southwestern Guizhou.Three mineralization stages,namely,the sedimentation diagenesis,hydrothermal(main-ore and late-ore substages),and supergene stages,were identified based on field and petrographic observations.The main-ore and late-ore stages correspond to Au and Sb mineralization,respectively,which are similar to typical Carlin-type mineralization.The mass transfer associated with alteration and mineralization shows that a significant amount of Au,As,Sb,Hg,Tl,Mo,and S were added to mineralized rocks during the main-ore stage.Remarkably,arsenic,Sb,and S were added to the mineralized rocks during the late-ore stage.Element migration indicates that the sulfidation process was responsible for ore formation.Four types of fluid inclusions were identified in ore-related quartz and fluorite.The main-ore stage fluids are characterized by an H2O–NaCl–CO2–CH4±N2system,with medium to low temperatures(180–260℃)and low salinity(0–9.08%NaCl equivalent).The late-ore stage fluids featured H2O–NaCl±CO2±CH4,with low temperature(120–200℃)and low salinity(0–7.48%Na Cl equivalent).The temperature,salinity,and CO2and CH4concentrations of ore-forming fluids decreased from the main-ore stage to the late-ore stage.The calculated δ^13C,d D,and δ^18O values of the ore-forming fluids range from-14.3 to-7.0%,-76 to-55.7%,and 4.5–15.0%,respectively.Late-ore-stage stibnite had δ^34S values ranging from-0.6 to 1.9%.These stable isotopic compositions indicate that the ore-forming fluids originated mainly from deep magmatic hydrothermal fluids,with minor contributions from strata.Collectively,the Baogudi metallogenic district has geological and geochemical characteristics that are typical of Carlin-type gold deposits in southwest Guizhou.It is likely that the Baogudi gold district,together with other Carlin-type gold deposits in southwestern Guizhou,was formed in response to a single widespread metallogenic event.     

Multi-episode fluid boiling in the Shizishan copper-gold deposit at Tongling, Anhui Province: its bearing on ore formation

The Shizishan copper-gold deposit at Tongling, Anhui Province consists of two magmato-hydrothermal mineralization types: the crypto-explosive breccia type and the skarn type. At least four episodes of boiling occurred to the ore-forming fluids in this deposit. The first episode took place in accompany with the formation of the crypto-explosive breccias. The melt-fluid inclusions giving temperatures above 600℃ and salinities higher than 42% NaCl equiv represent a residual magma related to this episode. The second episode occurred during skarnization, giving fluid temperatures of 422℃-472℃, averaging 458℃, and salinities of 10.2%-45.1% NaCl equiv. The third episode corresponds to the main mineralization stage, i.e., the quartz-sulphide stage. Fluid temperatures of this episode vary in a range of 337℃-439℃ with an average of 390℃, and salinities in a range of 3%-30% NaCl equiv. The forth episode happened at the waning stage of mineralization, giving fluid temperatures below 350℃ with an average of 265℃ and salinities of 2.1%-40.4% NaCl equiv.     

Two-phase separation and fracturing in mid-ocean ridge gabbros at temperatures greater than 700°C

Microthermometric analyses of fluid inclusions on a suite of hydrothermally altered gabbros recovered just south of the eastern intersection of the Kane Fracture Zone and the Mid-Atlantic Ridge, record the highest homogenization temperatures yet reported for mid-ocean ridge hydrothermal systems. Fluid salinities in the high temperature inclusions are more than ten times that of seawater. Multiple generations of fluid inclusions entrapped along healed microfractures exhibit three distinct temperature-compositional groups. We interpret these populations as having been trapped during three separate fracturing events.The earliest episode of brittle failure in the gabbros is represented by coplanar, conjugate vapor-dominated and brine-dominated fluid inclusion arrays in primary apatite. Vapor-dominated inclusions exhibit apparent homogenization temperatures of 400°C and contain equivalent salinities of 1–2 wt.% NaCl. These inclusions are interspersed with liquid-dominated, sulfide-bearing inclusions containing salinities of 50 wt.% NaCl equivalent. These high salinity inclusions remain unhomogenized at temperatures greater than 700°C.Compositional and phase relationships of the fluid inclusions may be accounted for by two-phase separation of a fluid under 1000–1200 bars pressure. These pressures require that fluid entrapment occurred under a significant lithostatic component and indicate a minimum entrapmentdepth of 2 km below the axial valley floor. This depth corresponds to a minimum tectonic uplift of 3 km, in order to emplace the samples at the 3100 m recovery depth. The microfracture networks within magmatic apatites represent fluid flow paths for either highly modified, deeply penetrating seawater or a late stage magmatic aqueous fluid. The inclusions may have formed close to the brittle-ductile transition zone adjacent to an active magma chamber.Following collapse of the high temperature front, lower temperature fluids of definite seawater origin circulated through the open fracture networks, pervasively altering portions of the gabbros. This stage is represented by low-to-moderate (1–7 wt.% NaCl equivalent) salinity inclusions in plagioclase, apatite, epidote, and augite, which homogenize at temperatures of approximately 200–300°C and 400°C. Formation of hydrous mineral assemblages, under greenschist to lower amphibolite facies conditions, resulted in sealing of the vein system and may have resulted in modification of seawater salinities by as much as a factor of two. During or following these later stages of hydrothermal activity the gabbros were emplaced high on the axial walls by differential uplift attending formation of the flanking mountains.     

Multi-stage fluid circulation in a hydraulic fracture breccia of the Larderello geothermal field (Italy)

The deep well MV5A, drilled in the western part of the Larderello geothermal field, crossed a 20-cm-thick hydraulic fracture breccia unit at a depth of 1090 m below ground level (b.g.l.). This breccia occurs in a fine-grained Triassic metasandstone and consists of angular to subangular clasts of up to some centimeters in size. Pervasive alteration has affected the breccia clasts and wall rock around the breccia, with the formation of Mg–Fe chlorite. After such alteration, hydrothermal circulation caused the precipitation of two generations of calcite cement. Then, ankerite partially replaced these two calcite generations. Ankerite also precipitated in late veinlets with chlorite. Late hydrothermal activity led to the crystallization of albite, quartz and finally, anhydrite. The calcite contains vapor-rich inclusions and two populations of liquid-rich (L1 and L2) inclusions. L1 inclusions are characterized by homogenization temperatures between 304 and 361°C and salinities from 7.4 to 11.6 wt.% NaCl equivalent; L2 inclusions revealed homogenization temperatures in the range of 189–245°C and salinities from 2.6 to 6.3 wt.% NaCl equivalent. The fluids contained in L2 inclusions were probably trapped coevally with some vapor-rich inclusions under boiling conditions after the L1 inclusions formed. Some of the abundant vapor-rich inclusions in calcite may also represent early, low-temperature inclusions affected by decrepitation and/or stretching and/or leaking during L1 trapping. The liquid-rich (L) inclusions trapped at later stages in ankerite, albite and anhydrite display, respectively, homogenization temperature ranges of 189–198°C, 132–145°C, and 139–171°C, and salinities ranging from 1.6 to 1.7 wt.% NaCl equivalent, 1.4 to 2.1 wt.% NaCl equivalent and 3.7 to 6.2 wt.% NaCl equivalent. The inclusions studied record the evolution, over time, of the fluids flowing in the breccia level: L1 inclusions capture high-temperature fluid (about 300 to 350°C) of high salinity (around 10 wt.% NaCl equivalent) at above-hydrostatic pressures (up to about 150 bar). The L2 inclusions in calcite and liquid-rich inclusions in ankerite and albite represent subsequent hydrothermal fluid evolution toward lower temperatures (about 250 to 130°C), pressures (45 to a few bar) and salinities (6.3 to 1.4 wt.% NaCl equivalent). During this stage, boiling processes and infiltration of meteoric waters probably occurred. Finally, moderately saline fluids (around 5 wt.% NaCl equivalent) at a temperature (about 160°C) close to that of present-day in-hole measurements was trapped in the anhydrite inclusions. The liquids trapped in liquid-rich inclusions circulated at 41,000 years (maximum age of calcite) or later. This age represents an upper limit for the development of vapor-dominated condition, in this part of the geothermal system. The fluids circulating at the breccia level were probably meteoric and/or connate waters. These fluids may have interacted with the anhydrite and carbonate bearing formations present in the Larderello area. The occurrence of the hot and saline fluids, trapped in L1 inclusions at above-hydrostatic pressure, suggests that similar fluids but with higher pressure (≥167 bar) and temperature (≥360°C) may have been responsible for rock fracturing.     

Regional metamorphism and hydrothermal alteration related to Miocene submarine volcanism ('green tuff') in the Yurihara oil and gas field, northwest Honshu Island, Japan

Abstract Alteration of reservoir rocks in the Yurihara Oil and Gas Field, hereafter referred to as the ‘Yurihara field’, have been examined by using samples from six wells. These rocks are basalts in the lowermost part of the basin-fills (‘green tuff’ Formation). These basalts were produced in many eruptions in a submarine environment during the early to middle Miocene, and they underwent continuous intensive alteration genetically associated with Miocene submarine volcanism. The alteration of the basalts is of two types: low grade metamorphism and hydrothermal. The former belongs to the type of ocean floor metamorphism and comprises two subgroups: zeolite (zone I) and prehnite-pumpellyite (zones IIa: vein and amygdule occurrence, and IIb: replacing plagioclase). The latter is characterized by potassic metasomatism accompanied by adularia, quartz and calcite veins (zones IIIa: center and IIIb: margin of the metasomatism). This overprints the low grade metamorphic alteration. The central zone of hydrothermal alteration coincides with a major estimated fault, so that fluids probably assent along the fault. The basalts erupted during 16.5-15.5 Ma, determined by planktonic foraminifera assemblages of inter-bedded shales, then underwent successive low grade metamorphism. In time, the hydrothermal alteration that overprints low grade metamorphism occurred. Adularia veins of the altered rocks located in the hydrothermal alteration zones (zone IIIa and IIIb) have been dated as 9 Ma determined by the K-Ar method. This fact indicates that the activity of low grade metamorphism had already crossed the peak before hydrothermal alteration occurred at 9 Ma. The shape of isotherms of fluid inclusion homogenization temperatures (Th) and that of isolines of apparent salinity (Tm) almost coincide with each other, and these also coincide with the distribution of hydrothermal alteration (zones IIIa and IIIb). This indicates that the fluid inclusions formed at the same time as ascending fluids produced the potassic metasomatism. The maximum Th of the fluid inclusions is 222°C and Tm indicates trapped fluids of up to 3.3 wt% equivalent NaCl (i.e. almost the same as seawater). A Th versus Tm plot indicates mixing occurred between hydrothermal fluids and formation water that has low salinity. Corrensite and chlorite form veins, and the temperatures of their formation, estimated by the extent of aluminium substitution into the tetrahedral site of chlorite, ranges between 165 and 245°C in the centre of the hydrothermal alteration zone (zone IIIa). This is consistent with the result of Th analyses. The deposition temperature of chlorite associated with prehnite in veins ranges between 190 and 215°C in zones IIa and IIb.     

Ore-forming fluid and metallization of the Huanggangliang skarn Fe-Sn deposit, Inner Mongolia

Two kinds of inclusions, fluid-melting inclusion and gas-liquid inclusion, are present in the Huanggangliang deposit in eastern Inner Mongolia. Temperature ranges from 1050°C of fluid-melting inclusion to 150°C of liquid inclusion. Away from intrusion, the inclusions of orebodies intend to be characterized by simpler type, lower temperature and lower salinity, as well as weakened relation to intrusion. The metallization of the Huanggangliang deposit is characterized by multiple activities of ore-forming fluid, multi-source, multi-stage accumulation of ore-forming material, F-rich environment, enrichment of F, organic gas, CO₂ and N₂, and involving of residual magma.     

The November 2002 eruption of Piton de la Fournaise,Réunion: tracking the pre-eruptive thermal evolution of magma using melt inclusions

The November 2002 eruption of Piton de la Fournaise in the Indian Ocean was typical of the activity of the volcano from 1999 to 2006 in terms of duration and volume of magma ejected. The first magma erupted was a basaltic liquid with a small proportion of olivine phenocrysts (Fo₈₁) that contain small numbers of melt inclusions. In subsequent flows, olivine crystals were more abundant and richer in Mg (Fo_83–84). These crystals contain numerous melt and fluid inclusions, healed fractures, and dislocation features such as kink bands. The major element composition of melt inclusions in this later olivine (Fo_83–84) is out of equilibrium with that of its host as a result of extensive post-entrapment crystallization and Fe²⁺ loss by diffusion during cooling. Melt inclusions in Fo₈₁ olivine are also chemically out of equilibrium with their hosts but to a lesser degree. Using olivine–melt geothermometry, we determined that melt inclusions in Fo₈₁ olivine were trapped at lower temperature (1,182 ± 1°C) than inclusions in Fo_83–84 olivine (1,199–1,227°C). This methodology was also used to estimate eruption temperatures. The November 2002 melt inclusion compositions suggest that they were at temperatures between 1,070°C and 1,133°C immediately before eruption and quenching. This relatively wide temperature range may reflect the fact that most of the melt inclusions were from olivine in lava samples and therefore likely underwent minor but variable amounts of post-eruptive crystallization and Fe²⁺ loss by diffusion due to their relatively slow cooling on the surface. In contrast, melt inclusions in tephra samples from past major eruptions yielded a narrower range of higher eruption temperatures (1,163–1,181°C). The melt inclusion data presented here and in earlier publications are consistent with a model of magma recharge from depth during major eruptions, followed by storage, cooling, and crystallization at shallow levels prior to expulsion during events similar in magnitude to the relatively small November 2002 eruption.     

Sources of ore-forming fluids and metallic materials in the Jinwozi lode gold deposit,eastern Tianshan Mountains of China

This paper presents gas compositions and H-, O-isotope compositions of sulfide- and quartz-hosted fluid inclusions, and S-, Pb-isotope compositions of sulfide separates collected from the principal Stage 2 ores in Veins 3 and 210 of the Jinwozi lode gold deposit, eastern Tianshan Mountains of China. Fluid inclusions trapped in quartz and sphalerite are dominantly primary. H-and O-isotopic compositions of pyrite-hosted fluid inclusions indicate two major contributions to the ore-forming fluid that include the degassed magma and the meteoric-derived but rock ¹⁸O-buffered groundwater. However, H- and O-isotopic compositions of quartz-hosted fluid inclusions essentially suggest the presence of groundwater. Sulfide-hosted fluid inclusions show considerably higher abundances of gaseous species CO₂, N₂, H₂S, etc. than quartz-hosted ones. The linear trends among inclusion gaseous species reflect the mixing tendency between the gas-rich magmatic fluid and the groundwater. The relative enrichment of gaseous species in sulfide-hosted fluid inclusions, coupled with the banded ore structure indicating alternate precipitation of quartz with sulfide minerals, suggests that the magmatic fluid has been inputted to the ore-forming fluid in pulsation. Sulfur and lead isotope compositions of pyrite and galena separates indicate an essential magma derivation for sulfur but the multiple sources for metallic materials from the mantle to the bulk crust.     

Sources of ore-forming fluids and metallic materials in the Jinwozi lode gold deposit,eastern Tianshan Mountains of China

This paper presents gas compositions and H-, O-isotope compositions of sulfide- and quartz-hosted fluid inclusions, and S-, Pb-isotope compositions of sulfide separates collected from the principal Stage 2 ores in Veins 3 and 210 of the Jinwozi lode gold deposit, eastern Tianshan Mountains of China. Fluid inclusions trapped in quartz and sphalerite are dominantly primary. H-and O-isotopic compositions of pyrite-hosted fluid inclusions indicate two major contributions to the ore-forming fluid that include the degassed magma and the meteoric-derived but rock ¹⁸O-buffered groundwater. However, H- and O-isotopic compositions of quartz-hosted fluid inclusions essentially suggest the presence of groundwater. Sulfide-hosted fluid inclusions show considerably higher abundances of gaseous species CO₂, N₂, H₂S, etc. than quartz-hosted ones. The linear trends among inclusion gaseous species reflect the mixing tendency between the gas-rich magmatic fluid and the groundwater. The relative enrichment of gaseous species in sulfide-hosted fluid inclusions, coupled with the banded ore structure indicating alternate precipitation of quartz with sulfide minerals, suggests that the magmatic fluid has been inputted to the ore-forming fluid in pulsation. Sulfur and lead isotope compositions of pyrite and galena separates indicate an essential magma derivation for sulfur but the multiple sources for metallic materials from the mantle to the bulk crust.

     

The ClBrI composition of 3.23 Ga modified seawater: implications for the geological evolution of ocean halide chemistry

Fluid inclusion leachates obtained from vug and vein quartz samples from an Archean (3.23 Ga) Fe-oxide hydrothermal deposit in the west-central part of the Barberton greenstone belt, South Africa, were analyzed by ion chromatography for chloride, bromide, and iodide. The deposit, known as the ironstone pods, formed by seafloor hydrothermal activity and fluid discharge. Quartz is dominated by type I liquid-vapor, aqueous inclusions with a bimodal salinity distribution (0–0.25 M_Cl⁻ and 0.9–1.8 M_Cl⁻). Bulk analytical salinities range from 0.45 to 0.99 M_Cl⁻ represent averages of type I inclusions. Bulk fluid inclusion bromide and iodide concentrations are 1.44–3.32 mM and 0.01–0.12 mM, respectively. For comparison, modern seawater has halogen contents of 590 mM chloride, 0.9 mM bromide, and 0.5 μM total iodine. In the fluids from the ironstone pods, bromide and iodide are enriched relative to chloride, when compared with modern seawater.Approximate Br⁻Cl⁻ and I⁻Cl⁻ ratios of 3.2 Ga Barberton seawater are 2.5 × 10⁻³ and 40 × 10⁻⁶, respectively. Dispersion to higher values was caused principally by reaction with organic sediments whose trends are similar to those seen for modern vent fluids at unsedimented and sedimented ridges, relative to modern seawater. These halide ratios are greater than those of modern seawater, suggesting a change in the halide ratios of seawater over geological time. The analytical data are consistent with a model in which marine organic sedimentation has fractionated bromine and iodine out of seawater relative to chloride, thereby causing the halide ratios of seawater to decrease from high early and mid-Archean values towards their present day values.     

Characteristics of melt inclusions in skarn minerals from Fe,Cu(Au) and Au(Cu) ore deposits in the region from Daye to Jiujiang

The skarns and skarn deposits are widely distributed at home and abroad. The skarn deposits include many kinds of ores and higher ore grade. Some of them are broad in scale. Scientists of ore deposits from different countries have paid and are paying grea…     

Hydrogen and oxygen isotope studies of metamorphic fluid-rock interactions in the Dabie Mountains

Hydrogen and oxygen isotope studies were carried out on mineral separates from high to ultrahigh pressure metamorphic rocks at Huangzhen and Shuanghe in the eastern Dabie Mountains, East China. The δ¹⁸O values of eclogites cover a wide range of −5‰ to+9‰, but the δD values of micas fall within a narrow range of −85% to −70‰. Both equilibrium and disequilibrium oxygen isotope fractionations were observed between quartz and the other minerals, with reversed fractionations between omphacite and garnet in some eclogite samples. The δ¹⁸ O values of −5‰ to −1‰ for some of the eclogites represent the oxygen isotope compositions of their protoliths which underwent meteoric water-rock interaction prior to plate subduction. The preservation of oxygen isotope heterogeneity in the eclogites implies a channelized flow of fluids during progressive metamorphism caused by rapid subduction. Retrograde metamorphism has caused oxygen and hydrogen isotope disequilibria between some of the minerals, but the fluid for retrograde reactions was internally buffered in the stable isotope compositions. Project supported by the Chinese Ministry of Science and Technology (Grant No. 95-Pre-39), the National Natural Science Foundation of China (Grant Nos. 49794042, 49473173 and 49453003) and the Chinese Academy of Sciences (Grant No. KZ951-A1-401-5)     

Evidence of fluid inclusion for thermal fluid-bearing hydrocarbon movements in Qiongdongnan Basin, South China Sea

Diagenetic research and inclusion observance indicate that there are seven types of inlcusion in the reservoirs in the Qiongdongnan Basin. Based on the fluorescence color, ratio of gas/liquid, formation temperature, salinity and organic component of fluid inclusions, three events of thermal fluid movement were found, and only the second and third events are relative to hydrocarbon migration and accumulation with the temperatures of 140–150°C and 170–190°C., respectively.The mechanism of gas migration in aqueous phase suggests that the discharging site of thermal fluid is the favourable location for natural gas accumulation. Project supported by the Natlonal Natural Science Foundation of China.     

Metallogenic geodynamic background of Mesozoic gold deposits in granite-greenstone terrains of North China Craton

The spatial distribution map of 65 mid-large gold-deposits hosted in the granite-greenstone terrains of the North China Craton is first drawn. These gold deposits mainly concentrate in the Mesozoic remobilized Yinshan-Yan-shan-Liaoning-Jilin intracontinental collisional orogenic belt, the northern Qinling and the Jiaodong Mesozoic collisional orogenic belts, and the Mesozoic intracontinental fault-magmatic belts developed along the Taihangshan and the Tan-Lu faults; their mineralizing time is predominantly Jurassic-Cretaceous, i. e. the Yanshanian. The metallogenic geodynamic background is exactly the compression-to-extension transition regime during continental collision. The results are partly from the project entitled “The main types of gold mineralizations in China and their metallogenic model” (89-El) supported by the Ministry of Metallurgical Industry of China, and projects “Geology and metallogenesis of the main type gold deposits in East Chinaⁿ” (Grant No. 9488010) and “Study on ore-forming fluids of the Wangfeng gold deposit, Xinjiang” supported by the National Natural Science Foundation of China (Grant No. 49672119).     

Origin of natural sulphur-bearing immiscible inclusions and H2S in oolite gas reservoir, Eastern Sichuan

Based on results of microscopic observation and laser Raman analysis about fluid inclusions, multiple special forms of immiscible inclusions that contain sulphur, liquid hydrocarbon, bitumen, etc. were discovered in samples collected from the H₂S gas reservoir-containing carbonates in the Lower Triassic Feixianguan Formation in the Jinzhu-Luojia area, Kai County, Sichuan Province. Based on the lithology and burial history of the strata involved as well as measurement results of homogenization temperature of fluid inclusions, bitumen reflectivity, etc., it is concluded that the H₂S in the gas reservoir resulted from the thermal reaction between hydrocarbons in reservoir and CaSO₄ in the gypsum-bearing dolostone section at the high temperature (140°C–17°C) oil-cracked gas formation stage in Late Cretaceous. Thereafter, research on a great number of immiscible inclusions in the reservoir reveals that elemental sulphur resulted from oxidation of part of the earlier-formed H₂S and further reaction between sulphates, hydrocarbons and H₂S in geological fluids in H₂S-bearing gas reservoir at a temperature of 86°C–89°C and a pressure of 340×10⁵Pa and during the regional uplift stage as characterized by temperature decrease and pressure decrease in Tertiary. Meanwhile, gypsum, anhydrite and calcite formed at this stage would trap particles like elemental sulphur and result in a variety of special forms of immiscible inclusions, and these inclusions would contain information concerning the complexity of the fluids in the reservoir and the origin of H₂S and natural sulphur in the gas reservoir.     

Fluid inclusions and preliminary studies of hydrothermal alteration in core hole PLTG-1, Platanares geothermal area, Honduras

The Platanares geothermal area in western Honduras consists of more than 100 hot springs that issue from numerous hot-spring groups along the banks or within the streambed of the Quebrada de Agua Caliente (brook of hot water). Evaluation of this geothermal area included drilling a 650-m deep PLTG-1 drill hole which penetrated a surface mantling of stream terrace deposits, about 550 m of Tertiary andesitic lava flows, and Cretaceous to lower Tertiary sedimentary rocks in the lower 90 m of the drill core.Fractures and cavities in the drill core are partly to completely filled by hydrothermal minerals that include quartz, kaolinite, mixed-layer illite-smectite, barite, fluorite, chlorite, calcite, laumontite, biotite, hematite, marcasite, pyrite, arsenopyrite, stibnite, and sphalerite; the most common open-space fillings are calcite and quartz. Biotite from 138.9-m depth, dated at 37.41 Ma by replicate ⁴⁰Ar/³⁹ Ar analyses using a continuous laser system, is the earliest hydrothermal mineral deposited in the PLTG-1 drill core. This mid-Tertiary age indicates that at least some of the hydrothermal alteration encountered in the PLTG-1 drill core occured in the distant past and is unrelated to the present geothermal system. Furthermore, homogenization temperatures (T_h) and melting-point temperatures (T_m) for fluid inclusions in two of the later-formed hydrothermal minerals, calcite and barite, suggest that the temperatures and concentration of dissolved solids of the fluids present at the time these fluid inclusions formed were very different from the present temperatures and fluid chemistry measured in the drill hole.Liquid-rich secondary fluid inclusions in barite and caicite from drill hole PLTG-1 have T_h values that range from about 20°C less than the present measured temperature curve at 590.1-m depth to as much as 90°C higher than the temperature curve at 46.75-m depth. Many of the barite T_h measurements (ranging between 114° and 265°C) plot above the reference surface boiling-point curve for pure water assuming hydrostatic conditions; however, the absence of evidence for boiling in the fluid inclusions indicates that at the time the minerals formed, the ground surface must have been at least 80 m higher than at present and underwent stream erosion to the current elevation. Near-surface mixed-layer illite-smectite is closely associated with barite and appears to have formed at about the same temperature range (about 120° to 200°C) as the fluid-inclusion T_hvalues for barite. Fluid-inclusion T_h values for calcite range between about 136° and 213°C. Several of the calcite T_h values are significantly lower than the present measured temperature curve. The melting-point temperatures (T_m) of fluid-inclusion ice yield calculated salinities, ranging from near zero to as much as 5.4 wt. % NaCl equivalent, which suggest that much of the barite and calcite precipitated from fluids of significantly greater salinity than the present low salinity Platanares hot-spring water or water produced from the drill hole.     

Strontium isotope geochemistry of the Lemachang independent silver ore deposit, northeastern Yunnan, China

Sr isotope geochemical studies (the 87Sr/86Sr and ?18O-87Sr/86Sr systems) on the wall rocks and ores from the Lemachang independent Ag deposit in northeastern Yunnan provide strong evidence that the ore-forming fluids had flown through radiogenetically Sr-enriched rocks or strata prior to their entry into the locus of ore precipitation, and water-rock interaction is the main mechanism of Ag ore precipitation. The radiogenetically Sr-enriched source region may be the Proterozoic basement (the Kunyang and Hekou groups). Moreover, the theoretical modeling of the Sr isotopic system indicates that the ore-forming fluids contain as much as 3×10?6 Sr with isotopic composition of Sr being 0.750 and that of oxygen 7.0‰. The ore-forming temperatures were estimated at 150-250℃ for the carbonate rock-type ores and at 200-260℃ for the clastic rock-type.