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1.
Abstract. The Onsen site is an active submarine hydrothermal system hosted by the Desmos caldera in the Eastern Manus Basin, Papua New Guinea. The hydrothermal fluid is very acidic (pH=1.5) and abundant native sulfur is deposited around the vent. The δ34 S values of native sulfur range from -6.5 to -9.3 %o. δ34 S values of H2 S and SO4 in the hydrothermal fluid are -4.3 to -9.9 %o and +18.6 to +20.0 %o, respectively. These δ34 S values are significantly lower than those of the other hydrothermal systems so far reported. These low δ34 S values and the acidic nature of the vent fluids suggest that volcanic SO2 gas plays an important role on the sulfur isotope systematic of the Onsen hydrothermal system. Relationship among the δ34 S values of S-bearing species can be successively explained by the model based on the disproportionation reaction starting from the volcanic SO2 gas. The predicted δ34 S values of SO2 agree with the measured whole rock δ34 S values. δD and δ18 O values of clay minerals separated from the altered rock samples also suggest the contribution of the magmatic fluid to the hydrothermal system. Present stable isotopic study strongly suggests that the Onsen hydrothermal site in the Desmos caldera is a magmatic submarine hydrothermal system. 相似文献
2.
Sulfur Isotope Geochemistry of the Supergiant Xikuangshan Sb Deposit, Central Hunan, China: Constraints on Sources of Ore Constituents 总被引：2，自引：0，他引：2
Dong-sheng Yang Masaaki Shimizu Hidehiko Shimazaki Xian-hua Li Qing-lin Xie 《Resource Geology》2006,56(4):385-396
Abstract. The supergiant Xikuangshan Sb deposit is located in the Middle to Upper Devonian limestone of central Hunan, China. Primary ores are composed of early-stage stibnite and calcite with rare pyrite, early main-stage stibnite and quartz, and late main-stage stibnite and calcite. New sulfur isotope data reveal the clustering of δ34 S values (+5 ∼ +8 %) for both early and late main-stage stibnite; a single early-stage stibnite exhibits δ34 S value (+7.5 %) identical to its main ore-stage counterparts and the coexisting calcite has almost unmodified carbon isotope composition (-4.4 %). The data suggest a probable common source of sulfur for stibnite that was deposited at different paragenetic stages. A much wider variation in δ34 S values for early main-stage stibnite (+3.5 to +16.3 %, av. +7.5 %) compared to that for late main-stage stibnite (+5.3 to +8.1 %, av. +6.2 %) can be interpreted to be due to local interaction of earlier ore fluid with Devonian host rocks. The previous studies show that the Precambrian basement contains elevated Sb concentrations, and two distinctive sulfur reservoirs with δ34 Spyrite values at ca. +11 ∼ +24 % and -7.0 ∼-11 %. The homogenizing effect for sulfur hydrothermally leached from the two reservoirs might have provided ore constituents for the Xikuangshan fluids. 相似文献
3.
Abstract: Carbonate rocks of Cambrian (18 samples) and lower-middle Ordovician (11 samples) ages from South Korea were analyzed for sulfur contents of structurally substituted sulfate (SSS) and sulfides and their δ34 S values. The δ34 S values of SSS ranging from +25.9 to +45.2 permil, are averaged as +33.6 and +33.5 permil for the Cambrian and Ordovician rocks, respectively, which indicate high δ34 S values of the Cambro-Ordovician seawater. The SSS contents in the carbonate rocks are low being 2.9 to 17.3 ppm S (averaged as 7.0 ppm S). Sulfide sulfur, on the contrary, is much abundant containing 3 to 1,880 ppm S and the δ34 S values range widely between –17.6 and +31.1 permil. Sulfide sulfur of the studied rocks excluding impure carbonates has an average content of 187 ppm S and δ34 S value of +12.8 permil (n=24). The estimated δ34 S (sulfate–sulfide) values, which range from 13.8 to 25.4 permil in general with a few exceptions from 36.5 up to 52.3 permil for some impure carbonates, may provide evidence for the persistent oceanic anoxia with its temporary recovery during the Cambro-Ordovician time.
The SSS and sulfide sulfurs have often higher δ34 S values than the Mesozoic-Cenozoic ore sulfur (Ishihara et al., 2000). Since carbonate rocks are very reactive with circulating hydrothermal ore solution, high δ34 S values of the Korean ore deposits might be caused to some extent by 34 S enrichment from the host carbonates, resulting in the low SSS contents observed. 相似文献
The SSS and sulfide sulfurs have often higher δ
4.
Abstract: In order to know the cause of the high δ34 S values of the Korean ore deposits (Ishihara et al., 2000), Geumseong molybdenum skarn deposit and related Jurassic granitoids and Cambro-Ordovician carbonates were selected for the δ34 S analyses. Two sulfide samples occurring in hydrothermal veins in fresh granitoids quarry at Songhaksan yielded δ34 S values of +6.9 and +8.8 permil. These are slightly higher than +5.3 permil δ34 S of the averaged rock sulfides for the Jurassic Daebo granitoids. Pyrite and molybdenite from the Geumseong deposit vary from +8.6 to +11.5 permil (average + 10.7 permil). The intruded carbonates contain very low amount of SSS (structurally substituted sulfate) as 2.9 to 8.1 ppm with high δ34 S values between +28.8 and + 40.0 permil, and sulfides sulfur of 52 to 779 ppm with variable δ34 S values between +3.2 and +22.5 per–mil. It is concluded that sulfur of the host carbonates was extracted and migrated into the skarn deposit at the time of the granitoid intrusion and the related hydrothermal convection, on the basis of the location of the skarn deposit occurring between the carbonates and Jurassic granitoids, and of very low contents of SSS sulfur in the carbonates. A part of SSS possibly contaminated into the Jurassic granite. 相似文献
5.
Abstract. Isotope composition of whole rock sulfur has been measured on 14 schists, 10 gneisses, 7 gabbroids, 7 granitoids and 2 sedimentary rocks, with of 9 sulfide (pyrite) sulfurs in gabbros and granitoids, from the southwestern part of the Ryeongnam Massif, Korea. The δ34 S values of schists range from -4.6 to +6.1 % (average +0.9 %), those of gneisses from -4.0 to +0.8 % (-1.9%), those of gabbroids from -2.3 to +3.7 % (+1.0 %), and those of granitoids from -5.9 to +3.2 % (-1.9 %). The δ34 S values of pyrite separated from gabbros and granitoids show rather heavier values ranging from +3.1 to +9.4 % with an average of+5.8%.
Though the δ34 S values of whole rock sulfur give wide range of -5.9 to +6.1 %, the average of about -0.5 % is close to the mantle value. The granitoids sampled at the central parts of intrusive bodies or at the contacts with other plutonic rocks tend to show positive values, while those sampled near the boundary with basement rocks such as granitic gneiss and por-phyroblastic gneiss show negative values. Though the reason of this tendency is not clear at present, the δ34 S values of some granitoids in this area seem to represent possible influence by the assimilation of country rocks, particularly of gneisses.
Average isotopic compositions of ore sulfur from individual metal deposits in the studied area are summarized to have a range of+1.0 to +7.8 % with an average value of+3.2 %. The values are consistent with the previous finding that the ore sulfur isotopic values of the Ryeongnam Massif are the lowest among the four tectonic belts in Korea; Gyeonggi Massif, Ogcheon Belt, Ryeongnam Massif, and Gyeongsang Basin. This feature may reflect the isotopic compositions of plutonic rocks and basements in this area, which are characterized by relatively low values around zero permil. 相似文献
Though the δ
Average isotopic compositions of ore sulfur from individual metal deposits in the studied area are summarized to have a range of+1.0 to +7.8 % with an average value of+3.2 %. The values are consistent with the previous finding that the ore sulfur isotopic values of the Ryeongnam Massif are the lowest among the four tectonic belts in Korea; Gyeonggi Massif, Ogcheon Belt, Ryeongnam Massif, and Gyeongsang Basin. This feature may reflect the isotopic compositions of plutonic rocks and basements in this area, which are characterized by relatively low values around zero permil. 相似文献
6.
Polymetallic Mineralization at the Nakakoshi Copper Deposits, Central Hokkaido, Japan 总被引：6，自引：0，他引：6
Abstract: Polymetallic mineralization at the Nakakoshi deposits, Kamikawa town, central Hokkaido, occur as fracture-filling veins in Cretaceous slate of the Hidaka Supergroup. Ten veins have been recognized in NE-SW and E-W directions. Sericite in altered slate which is the host of the deposits, was dated at 31. 1 Ma, Oligocene in age.
No. 9 vein consists of massive chalcopyrite ore with various kinds of minerals such as pyrite, pyrrhotite, arsenopyrite, sphalerite, tetrahedrite, Ag-minerals and Cu–Zn–Fe–In–Sn–S minerals, quartz and sericite. Chalcopyrite and pyrite contain sphalerite star and sphalerite with chalcopyrite emulsions. Maximum indium contents of sphalerite and the Cu–Zn–Fe–In–Sn–S minerals are 1. 8 and 16. 3 wt%, respectively. The sulfur isotopic ratios, δ34 S of ore minerals, range from –12. 9 to –9. 6%. Formation temperatures of the sulfide minerals are estimated as 300–500°C, based on the paragenesis and chemical compositions of the minerals. 相似文献
No. 9 vein consists of massive chalcopyrite ore with various kinds of minerals such as pyrite, pyrrhotite, arsenopyrite, sphalerite, tetrahedrite, Ag-minerals and Cu–Zn–Fe–In–Sn–S minerals, quartz and sericite. Chalcopyrite and pyrite contain sphalerite star and sphalerite with chalcopyrite emulsions. Maximum indium contents of sphalerite and the Cu–Zn–Fe–In–Sn–S minerals are 1. 8 and 16. 3 wt%, respectively. The sulfur isotopic ratios, δ
7.
Kosei Komuro Hiroshi Kubota Tokiyuki Sato Yoshimichi Kajiwara Shojiro Tanimura 《Resource Geology》2004,54(4):425-436
Abstract. A comprehensive investigation was carried out on the distribution of both trace fossils and sulfur isotopes in mud-stones in the Hokuroku district, northeast Japan, in the hope of delineating the depositional environment of the mudstones in which the Kuroko deposits are embedded. The mudstones are generally massive in structure and usually contain large trace fossils, being indicative of an aerobic biofacies. On the other hand, some mudstones in and above the Kuroko ore horizon are partly laminated and usually contain smaller trace fossils, being assignable to an anaerobic or dysaerobic biofacies. The δ34 S values of sulfides in the mudstones above and below the ore horizon range from -40 to -12 %o, indicating mostly oxic depositional conditions in equilibrium with the inferred aerobic biofacies. In the mudstones in the ore horizon, the δ34 S values exhibit regionally discriminated variations: -44 to -12 %o in areas far (>1 km) from the known Kuroko deposits and -24 to +6 %o in areas closer to them. The latter high δ34 S group implies the temporal occurrence of local anoxic basins in the vicinity of the known Kuroko deposits. At the time of late Nishikurosawa Stage (i.e. the currently assumed Kuroko metallogenic epoch), an intense oceanic stagnation is suggested to have taken place to form the local anoxic basins responsible for the formation and preservation of Kuroko deposits. This oceanic environmental event is considered to be most likely due to increasing biological productivity primarily triggered and enhanced by upwelling of NADW in the paleo-Sea of Japan at that time. 相似文献
8.
ABSTRACT
The mineralogy and isotope geochemistry of carbonate minerals in the Coorong area are determined by the water chemistry of different depositional environments ranging from seawater to evaporitically modified continental water. The different isotopic compositions of coexisting calcite and dolomite suggest that each of the above two minerals was formed from water of composition and origin unique to that specific mineral. In addition, the dolomite was not formed by simple solid state cation exchange.
The occurrence of two types of dolomite was shown by isotope analysis and SEM observations. The dolomite, which is isotopically light (δ13 C = -1 to -2% 0 ; δ18 O=+3 to +5%0 ) and of fine grain size (˜ 0·5 μm) probably precipitated under the influence of evaporitically modified continental water. Coarser grained dolomite (up to 4 μm) is isotopically heavier (δ13 C=+3 to +4%0 ; δ18 O=+5 to + 6%0 ) contains Mg in excess of Ca and was formed in or close to equilibrium with atmospheric CO2 probably by the dolomitization of aragonite. 相似文献
The mineralogy and isotope geochemistry of carbonate minerals in the Coorong area are determined by the water chemistry of different depositional environments ranging from seawater to evaporitically modified continental water. The different isotopic compositions of coexisting calcite and dolomite suggest that each of the above two minerals was formed from water of composition and origin unique to that specific mineral. In addition, the dolomite was not formed by simple solid state cation exchange.
The occurrence of two types of dolomite was shown by isotope analysis and SEM observations. The dolomite, which is isotopically light (δ
9.
Abstract. Sulfur isotope ratios are analyzed for a series of mudstones in a successive section in the Taiheizan area in the central Green Tuff region, northeast Japan. The δ34 S values for the Uyashinai Mudstone Member (Nishikurosawa stage), the Onnagawa Formation and the Funakawa Formation range from -45 to -14%, -20 to +4% and -30 to -10%, respectively. There is a marked positive shift in δ34 S values at the Nishikurosawa/Onnagawa boundary and an upward δ34 S-decreasing trend in the Onnagawa and Funakawa Formations. The present data provides evidence for environmental change in the form of stratification of the seawater, initiated at the Nishikurosawa/Onnagawa boundary and persisting during deposition of the Onnagawa Formation, followed by gradual oxygenation during deposition of the Funakawa Formation. 相似文献
10.
东川式铜矿的成矿作用及后期叠加改造:来自硫化物原位硫同位素的制约 总被引：2，自引：1，他引：1
沉积岩型层状铜矿床(SSC型)的成因争论聚焦在成矿作用主要集中在沉积成岩期并可能叠加有后期成矿作用,还是形成于成岩后盆地闭合过程和造山作用有关。产于扬子板块西缘的东川式铜矿是中国SSC型矿床的典型代表,这些矿床赋存在晚古元古界东川群岩石中,主要呈层状矿体产出,但也存在少量脉状矿体。文章选择东川铜矿田内因民、汤丹和滥泥坪3个典型矿床的层状和脉状矿体中硫化物(黄铁矿、黄铜矿、斑铜矿和辉铜矿)开展原位硫同位素组成的对比研究。实验结果表明,这些矿床的硫化物原位硫同位素组成分布范围较广:因民矿床层状硫化物的δ34S值分布于4.7‰~22.1‰,汤丹和滥泥坪矿床层状硫化物的δ34S值为-3.3‰~3.1‰;因民矿床脉状硫化物的δ34S值分布于21.0‰~30.7‰,汤丹和滥泥坪矿床脉状硫化物的δ34S值为-19.4‰~3.5‰。层状矿体和脉状矿体的硫化物硫同位素组成明显不同,表明形成2种产状矿体的硫来源不同。层状矿体较大的硫同位素组成差异指示了海相硫酸盐不同程度的热化学还原作用,表明初始成矿流体中的硫来源于循环盆地卤水中溶解的海相蒸发岩。脉状矿体的硫同位素组成则强烈受控于矿区的赋矿围岩,因民矿床硫化物中极高的硫同位素组成表明硫的来源为地层中的海相蒸发岩,而汤丹和滥泥坪矿床中亏损34S的特征则表明硫的来源为富含生物还原硫的碳质板岩。结合野外地质关系和前人研究成果,文章认为层状矿体和脉状矿体是2期独立成矿事件的产物,层状矿体形成于成岩作用时期,脉状矿体形成于后期独立的局部构造热成矿事件,也即SSC型矿床的成矿作用主要发生在成岩期,但普遍遭受后期热液活动的叠加,并且在不同的成矿期中可能存在着多阶段的成矿作用。 相似文献
11.
K-Ar Ages of Tin-Polymetallic Mineralization in the Oruro Mining District, Central Bolivian Tin Belt 总被引：2，自引：0，他引：2
Abstract. K-Ar age determinations were carried out on vein- and rock-forming minerals from five vein-type tin-polymetallic ore deposits of the Oruro mining district in the central part of the Bolivian tin belt. The sericite from vein selvedges and an altered host rock provides good estimates of the ages of hypogene mineralization, and supergene alunite and jarosite provide ages for erosional and weathering episodes. It is concluded that hypogene mineralization in the Oruro mining district took place during the early to middle Miocene: 15.8±0.8 Ma at San José, 20.1±l.l Ma at Morococala, 20.5±1.0 Ma at Avicaya, and 19.6±1.0 Ma at Llallagua. Fine grained supergene alunite (δ34 S = -10.1 960) and jarosite yield K-Ar ages of 6.7±0.7 Ma at Avicaya and 3.9±0.7 Ma at Bolivar, respectively, suggesting that erosion and chemical weathering were active at those times. 相似文献
12.
At the Kingking porphyry copper-gold deposit, Compostela Valley, south-eastern Mindanao, Philippines, bornite pods occur in the brecciated parts in the biotite diorite porphyry, together with the volcanic rock and diorite fragments without associated stockworks of quartz veinlets. These pods are generally elongated in shape and measure several centimeters across their longest axes. They are composed of bornite and chalcopyrite with traces of calaverite. The δ34 S of bornite and subordinate chalcopyrite of bornite pods ranging from −2.2‰ to +0.1‰ are similar to the δ34 S of sulfides associated with quartz veinlets such as bornite and chalcopyrite ranging from −4.7‰ to ±0.0‰. This suggests that the ultimate source of sulfur is identical for bornite pods and sulfides associated with quartz veinlets. Bornite pods are associated with volcanic rock and dioritic fragments in the brecciated portion of the biotite diorite porphyry. It was observed that some dioritic fragments contain quartz veinlets, which may indicate an earlier episode of mineralization. Fragments of the earlier dioritic intrusive rocks and the volcanic rocks, together with the sulfides were incorporated into the biotite diorite porphyry magma. A molten sulfide is possible for the composition between bornite and intermediate solid solution at ∼800°C. The sulfides from the earlier dioritic intrusive rocks in the molten state were segregated and then eventually coalesce to form the bornite pods in the brecciated section of the biotite diorite porphyry. 相似文献
13.
ABSTRACT The Tripoli Formation (Lower Messinian) in Sicily includes diatomites irregularly alternating with marl and carbonate beds and lies, stratigraphically, between the Tortonian pelagic marls and the evaporitic Calcare di base. The relationships between mineralogy, textural features and oxygen-carbon isotopic compositions of carbonate components point to a wide variability of depositional conditions and suggest that Tripoli sedimentation occurred in small basins characterized by periodic and marked restriction from the open sea.
The isotopic values of calcite and dolomite in the diatomites suggest an evolution from normal marine towards more restricted environments. Evaporating conditions are also indicated by the occurrence of anhydrite, length-slow chalcedonic quartz and moulds of gypsum. In a more advanced stage, the precipitation of heavy δ18 0 dolomite in the interstitial pores of fossil-poor diatomites denotes an environment with highly evaporated water. Mixing of meteoric and marine waters, on the other hand, might have favoured the precipitation of a dolomite characterized by relatively low δ18 0 and δ13 C values.
The deposition of marl and carbonate beds alternating with or overlying the diatomites took place in an environment with highly evaporated marine waters on the basis of δl18 O values of dolomite (up to + 9.10‰) and aragonite (up to + 5.83‰), occurrence of evaporitic minerals and lack of fossils. The presence at these levels of calcite with extremely negative δ13 C values (down to - 38.40‰), filling gypsum moulds, suggests activity of sulphate-reducing bacteria. Some aragonitic marls, however, bear evidence of deposition in relatively normal marine conditions. 相似文献
The isotopic values of calcite and dolomite in the diatomites suggest an evolution from normal marine towards more restricted environments. Evaporating conditions are also indicated by the occurrence of anhydrite, length-slow chalcedonic quartz and moulds of gypsum. In a more advanced stage, the precipitation of heavy δ
The deposition of marl and carbonate beds alternating with or overlying the diatomites took place in an environment with highly evaporated marine waters on the basis of δl
14.
The Tianqiao Pb-Zn ore deposit of Guizhou Province, China, is located in the mid-east of the Si-chuan-Yunnan-Guizhou Pb-Zn-Ag multi-metallic mineralization area, which is representative of the Pb-Zn ore de-posits in this area. It consists of three main orebodies, whose Pb+Zn reserves are more than 0.2 million ton. This paper analyzes the sulfur isotopic composition of these orebodies. The data show that the ore minerals (galena, sphalerite, pyrite) in these orebodies are enriched in heavy sulfur, with δ34SV-CDT values varying between 8.35‰ and 14.44‰, i.e. the δ34SV-CDT values of pyrite are between 12.81‰ and 14.44‰, the mean value is 13.40‰; the δ34SV-CDT values of sphalerite are range from 10.87‰ to 14.00‰, the mean value is 12.53‰; the δ34SV-CDT values of galena are range from 8.35‰ to 9.83‰, the mean value is 8.84‰, and they have the feature of δ34Spyrite>δ34Ssphalerite>δ34Sgalena, which indicates the sulfur isotope in ore-forming fluids has attained equilibrium. The δ34S V-CDT values of the deposit are close to those of sulfates from carbonate strata of different ages in the ore-field (15‰), which suggests that the sulfur in the ore-forming fluids should be derived from the thermo-chemical sulfate reduction of sulfates from the sedimentary strata. 相似文献
15.
Many different types of water and processes have been proposed for the formation of dolomites. The three phases of hydrothermal dolomites in the Middle Atlas Causse were investigated to elucidate their formation processes. The first two of these are associated with sphalerite and galena in stratiform and open space-filling deposits. These formed early in the history of the deposition of the Pb–Zn mineralization and commonly reveal a paragenetic overlap. A later phase, post-dating Pb–Zn mineralization, is reflected in saddle dolomite.
All three phases show a decrease in δ18 O and δ13 C values passing from sterile (unmineralized) to mineralized rocks, and isotopic signatures are independent of the carrier facies. However, early-formed dolomites can be separated into two distinct groups on the basis of δ18 O values. Type 1 dolomites host stratiform ore deposits, whereas type 2 dolomites host an open space-filling ore-body. Later saddle dolomites are more depleted in 18 O than either of these.
The early hydrothermal and saddle dolomites precipitated from similar fluids during three distinct events, but formed by two mechanisms: replacement (hydrothermal dolomite) and cement precipitation (saddle dolomite). They show different isotopic signatures and apparently formed at different temperatures. Field data, petrographic and stable isotope results suggest a continuum of replacement, during the Carixian for the early hydrothermal dolomite 1, and during the Toarcian for early hydrothermal dolomite 2, followed by a cement precipitation phase for saddle dolomite. 相似文献
All three phases show a decrease in δ
The early hydrothermal and saddle dolomites precipitated from similar fluids during three distinct events, but formed by two mechanisms: replacement (hydrothermal dolomite) and cement precipitation (saddle dolomite). They show different isotopic signatures and apparently formed at different temperatures. Field data, petrographic and stable isotope results suggest a continuum of replacement, during the Carixian for the early hydrothermal dolomite 1, and during the Toarcian for early hydrothermal dolomite 2, followed by a cement precipitation phase for saddle dolomite. 相似文献
16.
Abstract. Fluid inclusion and oxygen isotope studies are performed to obtain temperatures and oxygen isotopic compositions of hydrothermal fluids for the vein-type tungsten-copper deposit at Takatori in Ibaraki Prefecture, Japan. Temperatures of the hydrothermal fluids are calculated from fluid inclusion data. The calculation incorporates the effects of the salinity, gas concentration, and fluid pressure. The fluid temperatures range from 370 to 460C. For these calculations, this study obtains a density equation for H2 O-NaCl-CO2 solution at the vapor-liquid two-phase boundary. Then the present study combines the obtained equation with the equation of state by Bowers and Helgeson (1983).
The fluid temperatures determined in this study are applied to the calculation of oxygen isotopic compositions of the hydrothermal fluids. The calculation of the oxygen isotopic compositions is based on the oxygen isotope analyses of vein quartz. The oxygen isotopic compositions of vein quartz range from +13.5 to +14.4 % relative to SMOW. Then, the oxygen isotopic compositions of the hydrothermal fluids in equilibrium with the vein quartz are calculated to be from +9.7 to +10.5 %. These δ18 Ofluid values agree with those of magmatic fluids derived from the ilmenite-series granitic rock, which is related to the mineralization. Keywords: Takatori tungsten-copper deposit, fluid inclusion, oxygen isotope, vein quartz, H2 O-NaCl-CO2 solution, density 相似文献
The fluid temperatures determined in this study are applied to the calculation of oxygen isotopic compositions of the hydrothermal fluids. The calculation of the oxygen isotopic compositions is based on the oxygen isotope analyses of vein quartz. The oxygen isotopic compositions of vein quartz range from +13.5 to +14.4 % relative to SMOW. Then, the oxygen isotopic compositions of the hydrothermal fluids in equilibrium with the vein quartz are calculated to be from +9.7 to +10.5 %. These δ
17.
Oxygen Isotopic Characteristics of Granitic Intrusions Related to Haobugao Zn-Pb-Cu-Sn Skarn Deposit, East Inner Mongolia, China 总被引：2，自引：0，他引：2
Jingbin Wang Lijuan Wang Yuwang Wang Tiejun Li Hidehiko Shimazaki 《Resource Geology》2004,54(2):205-208
Abstract. Granitic rocks related to the formation of Haobugao Zn-Pb-Cu-Sn skarn deposit, Inner Mongolia, China, show unusual low whole-rock δ18 O values down to -8.8 % (V-SMOW), whereas separated quartz crystals from those rocks give positive δ18 O values of+4.1 to +9.9 %. Chemical analyses and microscopic observation of those granitic rocks confirm that they suffered hydrothermal alteration. Some skarn specimens and quartz from the Haobugao deposit also show negative δ18 O values. The isotopic evidence indicates that intensive meteoric water circulation occurred at the time of granitic intrusion, and caused the pervasive hydrothermal alteration of granitic rocks and the precipitation of skarn deposit in this area. 相似文献
18.
为了研究柞水—山阳矿集区夏家店金矿床成因,采用LA-ICP-MS和LA-MC-ICP-MS技术分析夏家店金矿床矿体及围岩样品中黄铁矿原位微量元素及氢、氧、硫同位素组成特征。结果表明,该矿床黄铁矿的Co/Ni 比值为0.11~0.76,说明其与沉积作用有关。矿石中黄铁矿的δ34S值(-9.40‰~7.16‰)与围岩碳质板岩的δ34S值(-8.84‰~10.64‰)接近,黄铁矿的δ34S均值(2.47‰)基本落在岩浆硫的范围内,指示矿石硫可能由地层硫和岩浆硫混合而成。氢、氧同位素测试结果表明,夏家店矿床成矿流体可能主要来自岩浆水,成矿后期有大气降水的加入。综合矿床地质特征、成矿温度、金赋存状态等特征和黄铁矿微量元素、硫同位素组成可知,夏家店金矿床属于卡林型金矿,其成矿流体主要来自岩浆水,成矿后期有大气降水加入;其成矿物质是由深部岩浆与地层混合而成。 相似文献
19.
陕西旬阳泗人沟铅锌矿床位于南秦岭褶皱系之大羊山复向斜南翼,赋存在上志留统水洞沟组第二岩性段的粉砂质千枚岩中。矿体受控于层间破碎带和劈理带,呈层状、似层状、透镜状产出。矿石矿物以闪锌矿、方铅矿、黄铁矿、磁黄铁矿和黄铜矿为主;矿石结构主要为它形-半自形粒状集合体结构、交代结构和固溶体分离结构;矿石构造主要为块状、条带状、浸染状和细脉状。激光剥蚀多接收等离子体质谱原位S同位素组成分析结果显示,矿石硫化物的硫同位素组成比较稳定,样品的δ34S值主要介于0.17‰~2.03‰之间,具有塔式分布特征,反映硫主要源于地幔和深部地壳,也有少量地层硫参与。9件矿石硫化物样品的206Pb/204Pb值为17.198~18.213,平均17.845;207Pb/204Pb值为15.564~15.627,平均15.610; 208Pb/204Pb值为37.982~38.471,平均38.206;反映铅同位素总体较稳定,变化范围较小,铅同位素主要源于上地壳,也有少量地幔铅参与。综合矿床地质、地球化学特征,认为泗人沟铅锌矿床成因类型属于后生热液充填交代型。 相似文献
20.
Stable Isotope Study of the Langshan Polymetallic Mineral District, Inner Mongolia, China 总被引：3，自引：0，他引：3
Abstract: A comprehensive stable isotope investigation was carried out to clarify the geneses of the ore deposits in the Langshan Pb-Zn mineral district. The lead isotope study shows that these deposits were probably formed from 2. 0 to 1. 5 Ga, and were deformed and metamorphosed 1. 45 Ga. Ore lead could be a mixture of mantle lead and crustal lead. The C and S isotope results indicate that these deposits were precipitated in closed or semi-closed rift basins, and the source of sulfur might be Proterozoic ocean sulfate. The H and O isotope results indicate that the δD and δ18 O values of rocks were changed by water-rock interaction during metamorphism and hydrothermal alteration. The scale of δD and δ18 O shift of rocks reflects the grade of metamorphism and alteration as well as the water-rock ratios. However, the water-rock ratios in the metamorphic processes of Langshan mineral district were relatively low, and the source of water during metamorphism is suggested to be ancient meteoric water. Based on isotopic results and the geological background, it is concluded that these deposits may belong to Proterozoic sedimentary exhalative (SEDEX) type. 相似文献