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1.
A fluid inclusion investigation of the polymetallic mineralization at Yinshan from the Le–De metallogenic belt in Jiangxi Province of China has been carried out using petrographic and microthermometric techniques. The data obtained here indicate that three major types of fluids were involved during the formation of the deposit. They are type I vapor-rich, type II liquid-rich and type III halite-bearing inclusions within the H2O–NaCl system. The high salinity fluids represented by type III inclusions, being unusual to the distal part of an intrusion-centered ore-forming system such as Yinshan, have been interpreted as the product of direct exsolution of a crystallizing magma, rather than a result of fluid immiscibility from a low salinity fluid. Evidence used to support such an interpretation includes the mode of homogenization of type III inclusions exclusively via halite dissolution, spatial separation of type I and type III inclusions on microscopic scale, the consistent phase ratios within the inclusions concerned, and considerable deviation in homogenization temperature for both type I and type III inclusions. Trapping conditions for type I inclusions were estimated to be around 440 °C and 260 bars, while type III inclusions were constrained to be trapped at least above 900 bars and > 500 °C. The formation temperatures for type II inclusions range from 270 to 390 °C if a lithostatic pressure of 260 bars is assumed. Pressure fluctuation determined by this fluid inclusion study coupled with decreases in salinity and temperature as result of the potential fluid mixing are supposed to have played an important role in triggering the precipitation of ore minerals from the hydrothermal solution.  相似文献   

2.
The Chalukou giant Mo deposit in the Heilongjiang Province, northeastern China, is a porphyry deposit hosted in an intermediate‐felsic complex surrounded by Mesozoic volcano–sedimentary rocks. The mineralization process is composed of four stages, including quartz + K‐feldspar (Stage I), quartz + molybdenite (Stage II), pyrite + chalcopyrite + quartz ± other sulphides (Stage III) and carbonate ± fluorite ± quartz (Stage IV). The mineralization is generally associated with intense K‐feldspar‐, fluorite‐, phyllic‐ and propylitic alteration. Primary fluid inclusions (FIs) in quartz include four compositional types, i.e. pure carbonic (PC‐type), aqueous‐carbonic (C‐type), daughter mineral‐bearing (S‐type) and aqueous (W‐type) inclusions. Halite, sylvite and hematite are recognized as the daughter minerals in Stage I S‐type FIs, whereas molybdenite and chalcopyrite occur as daughter minerals in Stage II S‐type FIs. High‐salinity and high pressure (>220 MPa) FIs exist in Stage I quartz veins, characterized by homogenization through halite dissolution at temperatures of 324 to 517 °C. The paucity of coexisting vapour‐rich FIs with similar homogenization temperatures at this stage indicates that the initial S‐type inclusions have directly exsolved from the magma rather than boiling off of a low‐salinity vapour. Stage I quartz has captured the C‐ and W‐type FIs, which have totally homogenized at 270–530 °C with salinities of 1.6–17.0 wt.% NaCl equiv. At Stage II, the coexistence of all FI types were only observed at pressures of 150–218 MPa and temperatures of 352–375 °C, with two salinity clusters of 0.9–16.6 wt.% NaCl equiv. and 37–56 wt.% NaCl equiv. Stage III quartz contains W‐type FIs with homogenization temperatures of 158–365 °C, salinities of 0.5–9.0 wt.% NaCl equiv., and minimum pressures of 12–116 MPa; whilst Stage IV fluorite or calcite only contains W‐type FIs with homogenization temperatures of 121–287 °C, salinities of 0.5–5.3 wt.% NaCl equiv., and minimum pressures of 10–98 MPa. The estimated trapping pressure from Stages II to III suggests an alternating lithostatic–hydrostatic fluid‐system caused by fluid boiling. Ore fluids at the Chalukou Mo deposit may have been evolved from a CO2‐rich, high‐salinity, and high‐oxygen fugacity (fO2) magma system, to a CO2‐poor, low‐salinity, and low‐fO2 epithermal system. Two key points may have contributed to the formation of the Chalukou giant Mo deposit: The magmatic origin and fluid boiling that has resulted in decompression and rapid precipitation of metals. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

3.
The Cobre–Babilonia vein system formed during a single major hydrothermal stage and is part of the Taxco district in Guerrero, southern Mexico. Homogenization and ice melting temperatures range from 160 to 290 °C and from − 11.6 to − 0.5 °C, respectively. We determined an approximate thermal gradient of 17 to 20 °C per 100 m using fluid inclusions. A thermal peak marked by the 290 °C isotherm is interpreted as a major feeder channel to the veins. The highest content of Zn + Pb in ore coincides with the 220 and 240 °C isotherms. Salinities of mineralizing fluids range from 0.8 to 15.6 wt.% NaCl equiv, and are distributed in two populations that can be related with barren or ore-bearing vein sections, with 0.8 to 6 wt.% NaCl equiv and 7 to 15.6 wt.% NaCl equiv, respectively. δ13C and δ18O water values from calcite from the Cobre–Babilonia vein system and the Esperanza Vieja and Guadalupe mantos range − 5.4‰ to − 10.4‰ and 9.9‰ to 13.4‰, respectively. δ34S values range from 0‰ to 3.2‰ and − 0.7‰ to − 4.3‰ in sphalerite, − 4‰ to 0.9‰ in pyrite, and − 1.4‰ to − 5.5‰ in galena. Both fluid inclusion and stable isotope data are compatible with magmatic and meteoric sources for mineralizing fluids. Also, sulfur isotope compositions suggest both magmatic and sedimentary sources for sulfur.  相似文献   

4.
The Katanga Copperbelt is the Congolese part of the well-known Central African Copperbelt, the largest sediment-hosted stratiform Cu–Co province on Earth. Petrographic examination of borehole samples from the Kamoto and Luiswishi mines in the Katanga Copperbelt recognized two generations of hypogene Cu–Co sulfides and associated gangue minerals (dolomite and quartz). The first generation is characterized by fine-grained Cu–Co sulfides and quartz replacing dolomite. The second generation is paragenetically later and characterized by coarse-grained Cu–Co sulfides and quartz overgrown and partly replaced by dolomite. Fluid inclusion microthermometric data were collected from two different types of fluid inclusions: type-I fluid inclusions (liquid + vapor) in the quartz of the first generation and type-II fluid inclusions (liquid + vapor + halite) in the quartz of the second generation. The microthermometric analyses indicate that the fluids represented by type-I and type-II fluid inclusions had very different temperatures and salinities and were not in thermal equilibrium with the host rock.Petrographic and microthermometric data indicate the presence of at least two main hypogene Cu–Co sulfide phases in the Katanga Copperbelt. The first is an early diagenetic typical stratiform phase, which produced fine-grained sulfides that are disseminated in the host rock and frequently concentrated in nodules and lenticular layers. This phase is related to a hydrothermal fluid with a moderate temperature (115 to 220 °C, or less if reequilibration of inclusions has occurred) and salinity (11.3 to 20.9 wt.% NaCl equiv.). The second hypogene Cu–Co phase produced syn-orogenic coarse-grained sulfides, which also occur disseminated in the host rock but mainly concentrated in a distinct type of stratiform nodules and layers and in stratabound veins and tectonic breccia cement. This second phase is related to a hydrothermal fluid with high temperature (270 to 385 °C) and salinity (35 to 45.5 wt.% NaCl equiv.).A review of available microthermometric and ore geochronological data of the Copperbelt in both the Democratic Republic of Congo and Zambia supports the regional presence of the two Cu–Co phases proposed in our study. Future geochemical analyses in the Copperbelt should take into account the presence of, at least, these two Cu–Co phases, their contrasting fluid systems and the possible overprint of the first phase by the second one.  相似文献   

5.
Mineralizing fluids at the San Martín skarn show an evolution characterized by prograde and retrograde associations. The prograde mineral associations consist of (1) a massive garnet zone, (2) a tremolite ± garnet zone, and (3) a late association of quartz, sphalerite, calcite and fluorite lining the vugs in the garnet zone. The fluids of the prograde associations exhibit decreasing temperatures of homogenization (Th) and variable salinities. The fluids of the massive garnet zone have salinities of 36 wt.% NaCl equiv. and Th of 645 to 570 °C, corresponding to pressures of 1055 bar. At the tremolite ± garnet zone, Th range from 438 to 354 °C. In the late association at the endoskarn, the following evolution can be drawn: (a) salinities of 50 to 42 wt.% NaCl equiv., and Th of 455 to 346 °C in quartz, (b) salinities of 46 wt.% NaCl equiv., and Th of 415 to 410 °C in sphalerite, (c) salinities of 50 to 37 wt.% NaCl equiv., and Th of 479 to 310 °C in calcite, (d) salinities of 33 to 28 wt.% NaCl equiv. and of 24 to 22 wt.% KCl in fluorite, and (e) two types of fluids with salinities of 2 and 39 wt.% NaCl equiv. and Th 344 and 300 °C, respectively, in later saccharoidal quartz segregations. The retrograde mineral associations comprise pervasive propylitic alteration to carbonization, and mantos with sulfides. Fluids in epidote have salinities of 7.6 wt.% NaCl equiv. and Th of 287 to 252 °C, and in calcite have salinities of 9.2 to 1 wt.% NaCl equiv. and Th of 188 to 112 °C. Fluids in the sulfide assemblages in the mantos have salinities of 8 to 3 wt.% NaCl equiv. and Th 300 °C, with corresponding pressures of 94 bar. Fluids in late epithermal veins close to the intrusive body have salinities of 10 to 5 wt.% NaCl equiv. and Th of 275 to 200 °C, and distal veins show salinities of 2 to 1 wt.% NaCl equiv. and Th of 160 °C.  相似文献   

6.
The Darreh‐Zereshk (DZ) and Ali‐Abad (AB) porphyry copper deposits are located in southwest of the Yazd city, central Iran. These deposits occur in granitoid intrusions, ranging in composition from quartz monzodiorite through granodiorite to granite. The ore‐hosting intrusions exhibit intense hydrofracturing that lead to the formation of quartz‐sulfide veinlets. Fluid inclusions in hydrothermal quartz in these deposits are classified as a mono‐phase vapor type (Type I), liquid‐rich two phase (liquid + vapor) type (Type IIA), vapor‐rich two phase (vapor + liquid) type (Type IIB), and multi‐phase (liquid + vapor + halite + sylvite + hematite + chalcopyrite and pyrite) type (Types III). Homogenization temperatures (Th) and salinity data are presented for fluid inclusions from hydrothermal quartz veinlets associated with potassic alteration and other varieties of hypogene mineralization. Ore precipitation occurred between 150° to >600°C from low to very high salinity (1.1–73.9 wt% NaCl equivalent) aqueous fluids. Two stages of hydrothermal activity characterized are recognized; one which shows relatively high Th and lower salinity fluid (Type IIIa; Th(L‐V) > Tm(NaCl)); and one which shows lower Th and higher salinity (Type IIIb; Th(L‐V) < Tm(NaCl)). The high Th(L‐V) and salinities of Type IIIa inclusions are interpreted to represent the initial existence of a dense fluid of magmatic origin. The coexistence of Type IIIb, Type I and Type IIB fluid inclusions suggest that these inclusions resulted either from trapping of boiling fluids and/or represent two immiscible fluids. These processes probably occurred as the result of pressure fluctuations from lithostatic to hydrostatic conditions under a pressure of 200 to 300 bar. Dilution of these early fluids by meteoritic water resulted in lower temperatures and low to moderate salinity (<20 wt% NaCl equiv.) fluids (Type IIA). Fluid inclusion analysis reveals that the hydrothermal fluid, which formed mineralized quartz veinlets in the rocks with potassic alteration, had temperatures of ~500°C and salinity ~50 wt% NaCl equiv. Cryogenic SEM‐EDS analyses of frozen and decrepitated ore‐bearing fluids trapped in the inclusions indicate the fluids were dominated with NaCl, and KCl with minor CaCl2.  相似文献   

7.
Tin-polymetallic greisen-type deposits in the Itu Rapakivi Province and Rondônia Tin Province, Brazil are associated with late-stage rapakivi fluorine-rich peraluminous alkali-feldspar granites. These granites contain topaz and/or muscovite or zinnwaldite and have geochemical characteristics comparable to the low-P sub-type topaz-bearing granites. Stockworks and veins are common in Oriente Novo (Rondônia Tin Province) and Correas (Itu Rapakivi Province) deposits, but in the Santa Bárbara deposit (Rondônia Tin Province) a preserved cupola with associated bed-like greisen is predominant. The contrasting mineralization styles reflect different depths of formation, spatial relationship to tin granites, and different wall rock/fluid proportions. The deposits contain a similar rare-metal suite that includes Sn (±W, ±Ta, ±Nb), and base-metal suite (Zn–Cu–Pb) is present only in Correas deposit. The early fluid inclusions of the Correas and Oriente Novo deposits are (1) low to moderate-salinity (0–19 wt.% NaCl eq.) CO2-bearing aqueous fluids homogenizing at 245–450 °C, and (2) aqueous solutions with low CO2, low to moderate salinity (0–14 wt.% NaCl eq.), which homogenize between 100 and 340 °C. In the Santa Bárbara deposit, the early inclusions are represented by (1) low-salinity (5–12 wt.% NaCl eq.) aqueous fluids with variable CO2 contents, homogenizing at 340 to 390 °C, and (2) low-salinity (0–3 wt.% NaCl eq.) aqueous fluid inclusions, which homogenize at 320–380 °C. Cassiterite, wolframite, columbite–tantalite, scheelite, and sulfide assemblages accompany these fluids. The late fluid in the Oriente Novo and Correas deposit was a low-salinity (0–6 wt.% NaCl eq.) CO2-free aqueous solution, which homogenizes at (100–260 °C) and characterizes the sulfide–fluorite–sericite association in the Correas deposit. The late fluid in the Santa Bárbara deposit has lower salinity (0–3 wt.% NaCl eq.) and characterizes the late-barren-quartz, muscovite and kaolinite veins. Oxygen isotope thermometry coupled with fluid inclusion data suggest hydrothermal activity at 240–450 °C, and 1.0–2.6 kbar fluid pressure at Correas and Oriente Novo. The hydrogen isotope composition of breccia-greisen, stockwork, and vein fluids (δ18Oquartz from 9.9‰ to 10.9‰, δDH2O from 4.13‰ to 6.95‰) is consistent with a fluid that was in equilibrium with granite at temperatures from 450 to 240 °C. In the Santa Bárbara deposit, the inferred temperatures for quartz-pods and bed-like greisens are much higher (570 and 500 °C, respectively), and that for the cassiterite-quartz-veins is 415 °C. The oxygen and hydrogen isotope composition of greisen and quartz-pods fluids (δ18Oqtz-H2O=5.5–6.1‰) indicate that the fluid equilibrated with the albite granite, consistent with a magmatic origin. The values for mica (δ18Omica-H2O=3.3–9.8‰) suggest mixing with meteoric water. Late muscovite veins (δ18Oqtz-H2O=−6.4‰) and late quartz (δ18Omica-H2O=−3.8‰) indicate involvement of a meteoric fluid. Overall, the stable isotope and fluid inclusion data imply three fluid types: (1) an early orthomagmatic fluid, which equilibrated with granite; (2) a mixed orthomagmatic-meteoric fluid; and (3) a late hydrothermal meteoric fluid. The first two were responsible for cassiterite, wolframite, and minor columbite–tantalite precipitation. Change in the redox conditions related to mixing of magmatic and meteoric fluids favored important sulfide mineralization in the Correas deposit.  相似文献   

8.
Gold-copper-bismuth mineralization in the Tennant Creek goldfield of the Northern Territory occurs in pipe-like, ellipsoidal, or lensoidal lodes of magnetite ± hematite ironstones which are hosted in turbiditic sedimentary rocks of Proterozoic age. Fluid inclusion studies have revealed four major inclusion types in quartz associated with mineralized and barren ironstones at Ten nant Creek; (1) liquid-vapour inclusions with low liquid/vapour ratios (Type I), (2) liquid-vapour inclusions with high liquid/vapour ratios or high vapour/liquid ratios and characteristic dark bubbles (Type II), (3) liquid-vapour-halite inclusions (Type III), and (4) liquid-vapour inclusions with variable liquid/vapour ratios (Type V). Type I inclusions are present in the barren ironstones and the unmineralized portions of fertile ironstones, whereas Types II and III inclusions are recognized in fertile ironstones. Trails of Types II and III inclusions cut trails of Type I inclusions. Type I fluid inclusions have homogenization temperatures of 100° to 350 °C with a mode at 200° to 250 °C. Type II inclusions in mineralized ironstones (e.g. Juno, White Devil, Eldorado, TC8 and Gecko K-44 deposits) have homogenization temperatures of 250 °C to 600 °C with a mode of 350 °C. Type I fluid inclusions have a salinity range of 10 to 30 NaCl equiv. wt %. Salinity measurements on fluid inclusions in the mineralized zones gave a range of 10 to 50 NaCl equiv. wt % with a mode of 35 NaCl equiv. wt %. Fluid inclusion studies indicate that the Tennant Creek ironstones were formed from a relatively low temperature and moderately saline fluid, where as gold and copper mineralization was deposited from later hydrothermal fluids of higher temperature and salin ity. Gas analysis indicates the presence of N2 and CO2, with very minor CH4 in Types II inclusions but no N2 or CH4 gases in Type I inclusions. Microprobe analysis of the fluid inclusion decrepitates indicates that the inclusions from Tennant Creek contain sodium and calcium as dominant cations and potassium in a subordinate amount. The high temperatures ( 350 °C), high salinities ( 35 NaCl equiv. wt. %) and cation composition of the Tennant Creek ore fluids suggest that the ore fluids were derived from upward migrating heated basinal brines, although contribution from a magmatic source cannot be ruled out. Close association of vapour-rich Type IIb and salt-rich Type III inclusions in the mineralized ironstones (e.g. Juno, White Devil, Eldorado, TC8 and Gecko K-44) indicates heterogeneous trapping of ore fluids. This heterogeneous trapping is interpreted to be due to unmixing (exsolution) of a gas-rich (e.g. N2) fluid during the upward migration of the metal bearing brines and/or due to degassing caused by reaction of oxidized ore fluids and host ironstones. Fluid inclusion data have important implications regarding the deposition of gold in the ironstones, and may have application in discriminating fertile from barren ironstones.  相似文献   

9.
The Zaldívar porphyry copper deposit, Northern Chile, consists of two major intrusions, the 290 Ma Zaldívar, and the more recent Miocene (38.7 Ma) Llamo porphyry. Five types of inclusions have been identified in quartz phenocrysts from Llamo porphyry, including melt inclusions (M), and four types of fluid inclusions, called MS (multi solids), B (brines), G (vapor-rich) and W (aqueous), respectively.Melt remnants, well preserved as M-inclusions, homogenize around 1000 °C. They show a rhyolitic composition, comparable to the most evolved acidic rhyolitic end member found elsewhere in the regional magmatism and to worldwide volcanic rhyolitic glass. High silica content in some inclusions can, however, be due to partial remelting of the quartz host during the heating run. Copper content in the same inclusions ranges between 0.03 and 0.57 wt.%, with an average concentration of 0.10 wt.%, suggesting a major magmatic source for the copper (orthomagmatic model).MS inclusions, which contain a number of solids at room temperature, mostly H2O-bearing phases (system NaCl–KCl–((Fe, Mg, Cu)Cl)–H2O, average salinity 70 wt.% NaCl equiv.), homogenize at magmatic temperatures (around 1000 °C). They represent the first fluids to have exsolved from the magma at depth, at a pressure of about 2 kbar. Their high homogenization temperature, comparable to values measured for melt inclusions (1000 to 1050 °C), may indicate trapping of MS and M inclusions in host phenocrysts from an immiscible mixture of silicate melt and highly saline fluids expelled from the magma during the early stage of quartz crystallization.The data indicate a magmatic origin for copper, as well as extremely high melt temperatures. These features are interpreted by magmatic differentiation of mantle-derived primitive melts, corresponding to major changes in the tectonic regime of the Andean margin, which occurred in Miocene times.  相似文献   

10.
The Phu Lon skarn Cu–Au deposit is located in the northern Loei Fold Belt (LFB), Thailand. It is hosted by Devonian volcano-sedimentary sequences intercalated with limestone and marble units, intruded by diorite and quartz monzonite porphyries. Phu Lon is a calcic skarn with both endoskarn and exoskarn facies. In both skarn facies, andradite and diopside comprise the main prograde skarn minerals, whereas epidote, chlorite, tremolite, actinolite and calcite are the principal retrograde skarn minerals.Four types of fluid inclusions in garnet were distinguished: (1) liquid-rich inclusions; (2) daughter mineral-bearing inclusions; (3) salt-saturated inclusions; and (4) vapor-rich inclusions. Epidote contains only one type of fluid inclusion: liquid-rich inclusions. Fluid inclusions associated with garnet (prograde skarn stage) display high homogenization temperatures and moderate salinities (421.6–468.5 °C; 17.4–23.1 wt% NaCl equiv.). By contrast, fluid inclusions associated with epidote (retrograde skarn stage) record lower homogenization temperatures and salinities (350.9–399.8 °C; 0.5–8 wt% NaCl equiv.). These data suggest a possible mixing of saline magmatic fluids with external, dilute fluid sources (e.g., meteoric fluids), as the system cooled. Some fluid inclusions in garnet contain hematite daughters, suggesting an oxidizing magmatic environment. Sulfur isotope determinations on sulfide minerals from both the prograde and retrograde stages show a uniform and narrow range of δ34S values (?2.6 to ?1.1 δ34S), suggesting that the ore-forming fluid contained sulfur of orthomagmatic origin. Overall, the Phu Lon deposit is interpreted as an oxidized Cu–Au skarn based on the mineralogy and fluid inclusion characteristics.  相似文献   

11.
Fluid inclusion data are presented for the successive stages of limestone, dolomite, magnesite and sulphide-bearing quartz veins in Proterozoic carbonate rocks of the Lesser Himalaya. Subsurface fluids were H2O–NaCl–KCl ± MgCl2 ± CaCl2 and showed successive increase in salinity and temperature. The salinity of the pore fluid during limestone diagenesis was in the range of 7.5–15 eq wt.% NaCl and the magnesite-forming fluids had a salinity of about 9 to 19 eq wt.% NaCl. This progressive rise in salinity is attributed to a more saline fluid in the deeper zones. The inverse relation between homogenization temperatures and final melting temperatures suggests mixing of the fluids during diagenesis, and highly depleted δ18O values rule out participation of magmatic fluid in the mixing. A late stage carbonic fluid is linked with talc formation. The low temperature of sulphide-forming epigenetic solutions, as obtained from fluid inclusions, is also substantiated by the chemical data from these sulphides. δ34S values in galena infer that magmatic sulphur was probably not involved, and the sulphur of the galena is derived from an isotopically heavy source.  相似文献   

12.
The Xihuashan tungsten deposit, Jiangxi province, China, is a world-class vein-type ore deposit hosted in Cambrian strata and Mesozoic granitic intrusions. There are two major sets of subparallel ore-bearing quartz veins. The ore mineral assemblage includes wolframite and molybdenite, with minor amounts of arsenopyrite, chalcopyrite, and pyrite. There are only two-phase aqueous-rich inclusions in wolframite but at least three major types of inclusions in quartz: two- or three-phase CO2-rich inclusions, two-phase pure CO2 inclusions and two-phase aqueous inclusions, indicating boiling. Fluid inclusions in wolframite have relatively higher homogenization temperatures and salinities (239–380°C, 3.8–13.7 wt.% NaCl equiv) compared with those in quartz (177–329°C, 0.9–8.1 wt.% NaCl equiv). These distinct differences suggest that those conventional microthermometric data from quartz are not adequate to explain the ore formation process. Enthalpy–salinity plot shows a linear relationship, implying mixing of different sources of fluids. Although boiling occurred during vein-type mineralization, it seems negligible for wolframite deposition. Mixing is the dominant mechanism of wolframite precipitation in Xihuashan. δ34S values of the sulfides range from −1.6 to +0.1‰, indicative of a magmatic source of sulfur. δ18O values of wolframite are relatively homogeneous, ranging from +4.8‰ to +6.3‰. Oxygen isotope modeling of boiling and mixing processes also indicates that mixing of two different fluids was an important mechanism in the precipitation of wolframite.  相似文献   

13.
Kyanite eclogites occur as part of the Münchberger nappe pile in NE-Bavaria, West Germany. Eclogites are overprinted by subsequent amphibolite facies metamorphism. The preservation of primary eclogitic textures as well as symplectitic textures are indicative of rapid decompression. Eclogite formation is estimated to have occurred under conditions of high H2O-activities at pressures between 20 and 26 kbar and temperatures ranging between 590 and 660° C, as is shown by the coexistence of omphacite (Jd 50), kyanite, zoisite and quartz. Minimum pressure estimates, independent of the water activity, range between 9 and 16 kbar at the relevant temperatures. Detailed studies of fluid inclusion reveal two predominant groups of aqueous-brine inclusions: high salinity (14–17 wt% NaCl equiv.) and low salinity (0–8 wt% NaCl equiv.) inclusions. Fluid compositions of both groups of inclusions yield isochores passing close to the estimated amphibolite facies PT-field. The compositions of these fluids are in good agreement with fluid compositions considered from mineral equilibria. None of the fluid inclusions has densities appropriate for eclogite facies metamorphism, but probably reflect later amphibolite facies metamorphism.  相似文献   

14.
Numerous gold deposits and occurrences were recognized in the regions of tectonomagmatic activation in the southeastern Siberian Platform. They are located in four metallogenic zones: the Ket-Kap (skarns, quartz veins, and stockworks; gold-bearing lodes in silicitolites; and argillisite-sericite metasomatites), Ulkan (clayey-micaceous metasomatites, quartz veins), Preddzhugdzhur (quartz veins, skarns, and sericite-hydromicaceous metasomatites), and Uda (sericite-hydromicaceous metasomatites). The skarn mineralization is of Meosozoic age, while the mineralization in the quartz veins, quartz-hydromicaceous metasomatites, and quartz-sulfide veins may have a Meosozoic, Paleozoic, or Late Paleozoic age. The highest temperatures were determined for the ore formation in the Preddzhugdzhur skarns (500–715 °C) and the hydrothermal-metasomatic rocks of the Ket-Kap zone (510–530 °C). The composition of gas-liquid inclusions in the minerals of these rocks is dominated by aqueous Na, K, and Ca chloride solutions with salinity up to 40 wt % NaCl equiv; fluid contains CO2. Quartz veins and stockworks of the Ket-Kap zone were formed under high (up to 465°C) and moderate temperatures and salinity up to 32 wt % NaCl equiv. Sometimes, the minerals in these rocks contain inclusions of low-density CO2. The gold-bearing veins of the Preddzhugdzhur zone formed at 225–230°C and salinity of 1–2 wt % NaCl equiv. The ore-bearing solutions in the gold-bearing veins of the Ulkan zone are characterized by a potassium-sodium-chlorine composition and salinity of 2–10 wt % NaCl equiv., and the temperature of their formation was 220–280 °C.  相似文献   

15.
The newly discovered Handagai skarn Fe–Cu deposit is located in the northern Great Xing'an Range of NE China and is hosted by the Ordovician Luohe Formation. The orebodies that form the deposit are generally concordant with the bedding within these sediments, and are spatially related to areas of skarn development. The Fe–Cu mineralization in this area records four stages of paragenesis, namely prograde skarn, retrograde skarn, quartz–sulfide, and quartz–carbonate stages. The Handagai deposit is a calcic skarn that is dominated by an andradite–diopside–epidote–actinolite assemblage. The mineralogy and geochemistry of the skarn indicate that it formed from a hydrothermal fluid that altered the carbonate units in this area to a garnet (And42–95Grs4–53) and pyroxene (Di71–78Hd22–29Jo0–2) bearing skarn. The epidote within the skarn has an epidote end-member composition, with the chlorite in the skarn dominantly Fe-rich, indicating that these minerals formed in an Fe-rich environment. The petrographic, microthermometric, and Raman spectroscopic analysis of fluid inclusions within garnet, epidote, actinolite, quartz, and calcite precipitated at different stages of formation of the Handagai deposit indicate that mineralization-related fluid inclusions are either liquid-rich two-phase H2O–NaCl (type I), gas-rich two-phase H2O–NaCl (type II), three-phase (liquid + vapor + solid) H2O–NaCl (type III), or CO2–H2O–NaCl inclusions (type IV). The early stages of mineralization are associated with all four types of inclusion, whereas the later stages of mineralization are only associated with type I and II inclusions. Inclusion homogenization temperatures vary between the four stages of mineralization (370 °C–530 °C and > 600 °C, 210 °C–290 °C, 190 °C–270 °C, and 150 °C–230 °C, from early to late, respectively), with salinities also varying between the earlier and later stages of mineralization (11–18 and > 45, 7–15, 6–9, and 3–7 wt.% NaCl equivalent (equiv.), respectively). The majority of the inclusions within the Handagai deposit have homogenization temperatures and salinities of 200 °C–350 °C and 4–14 wt.% NaCl equiv., respectively, indicating that this is a medium–high temperature and medium–low salinity type deposit. The fluid inclusions were trapped at pressures of 11 to 72 MPa, corresponding to depths of 0.4 to 2.9 km. The geology, mineralogy, geochemistry, and fluid inclusions microthermometry indicate that the Handagai deposit formed as a result of contact infiltration metasomatism, with the deposition of ore minerals resulting from a combination of factors that include boiling as a result of reduced pressure, cooling, and fluid mixing.  相似文献   

16.
甲玛铜多金属矿床位于西藏冈底斯斑岩铜矿带东段,是近年来勘探发现的超大型斑岩-矽卡岩型铜多金属矿床。通过冷热台显微观察与测温、扫描电镜、激光拉曼探针测试,对甲玛矿床各成矿阶段典型矿物的流体包裹体研究表明,成矿流体富含挥发分,临界相均一的流体来自岩浆超临界流体出溶,主成矿阶段具有沸腾包裹体组合特征,有机质包裹体荧光效应显著。显微测温结果显示,岩浆-热液阶段斑岩中石英斑晶的流体包裹体均一温度范围为250~540℃,含石盐子晶高盐度包裹体盐度范围为35~61(wt%)NaCl.eq,中等盐度的临界均一的气液包裹体盐度范围为3~29(wt%)NaCl.eq,岩浆期后热液阶段斑岩、角岩中石英脉的流体包裹体均一温度范围为210~410℃,盐度范围为33~41(wt%)NaCl.eq,与其不混溶共生的中低盐度气液两相流体包裹体盐度范围为5~25(wt%)NaCl.eq。矽卡岩阶段矿物均一温度范围为130~360℃,盐度范围为3~41(wt%)NaCl.eq,从岩浆热液过渡阶段到石英-硫化物阶段均一温度与盐度呈阶梯式降低趋势。斑岩体石英的流体包裹体中含有较多黄铜矿子矿物,岩浆结晶分异过程中已经具成矿元素的富集。激光拉曼探针测试结果显示,成矿早期至主成矿期矿物流体包裹体气相成分主要为CO2、CH4和N2,各阶段矿物流体包裹体气相成分具有继承性。成矿流体为高温度高盐度,富含CO2、CH4的流体。成矿流体主要源于岩浆,后期混有大气降水。当岩浆热液上升时因压力的突然释放造成高温含矿热流体发生减压沸腾,CO2和CH4等气体大量逃逸,导致成矿物质快速沉淀。矿床在成因上与岩浆-热液成矿作用密切相关。  相似文献   

17.
The Haobugao deposit, located in the southern segment of the Great Xing'an Range, is a famous skarn‐related Pb‐Zn‐(Cu)‐(Fe) deposit in northern China. The results of our fluid inclusion research indicate that garnets of the early stage (I skarn stage) contain three types of fluid inclusions (consistent with the Mesozoic granites): vapor‐rich inclusions (type LV, with VH2O/(VH2O + LH2O) < 50 vol %, and the majority are 5–25 vol %), liquid‐rich two‐phase aqueous inclusions (type VL, with VH2O/(VH2O + LH2O) > 50 vol %, the majority are 60–80 vol %), and halite‐bearing multiphase inclusions (type SL). These different types of fluid inclusions are totally homogenized at similar temperatures (around 320–420°C), indicating that the ore‐forming fluids of the early mineralization stage may belong to a boiling fluid system. The hydrothermal fluids of the middle mineralization stage (II, magnetite‐quartz) are characterized by liquid‐rich two‐phase aqueous inclusions (type VL, homogenization temperatures of 309–439°C and salinities of 9.5–14.9 wt % NaCl eqv.) that coexist with vapor‐rich inclusions (type LV, homogenization temperatures of 284–365°C and salinities of 5.2–10.4 wt % NaCl eqv.). Minerals of the late mineralization stage (III sulfide‐quartz stage and IV sulfide‐calcite stage) only contain liquid‐rich aqueous inclusions (type VL). These inclusions are totally homogenized at temperatures of 145–240°C, and the calculated salinities range from 2.0 to 12.6 wt % NaCl eqv. Therefore, the ore‐forming fluids of the late stage are NaCl‐H2O‐type hydrothermal solutions of low to medium temperature and low salinity. The δD values and calculated δ18OSMOW values of ore‐forming fluids of the deposit are in the range of ?4.8 to 2.65‰ and ?127.3‰ to ?144.1‰, respectively, indicating that ore‐forming fluids of the Haobugao deposit originated from the mixing of magmatic fluid and meteoric water. The S‐Pb isotopic compositions of sulfides indicate that the ore‐forming materials are mainly derived from underlying magma. Zircon grains from the mineralization‐related granite in the mining area yield a weighted 206Pb/238U mean age of 144.8 ±0.8 Ma, which is consistent with a molybdenite Re‐Os model age (140.3 ±3.4 Ma). Therefore, the Haobugao deposit formed in the Early Cretaceous, and it is the product of a magmatic hydrothermal system.  相似文献   

18.
Fluid inclusion microthermometry and structural data are presented for quartz vein systems of a major dextral transcurrent shear zone of Neoproterozoic–Cambrian age in the Ribeira River Valley area, southeastern Brazil. Geometric and microstructural constraints indicate that foliation–parallel and extensional veins were formed during dextral strike–slip faulting. Both vein systems are formed essentially by quartz and lesser contents of sulfides and carbonates, and were crystallized in the presence of CO2–CH4 and H2O–CO2–CH4–NaCl immiscible fluids following unmixing from a homogeneous parental fluid. Contrasting fluid entrapment conditions indicate that the two vein systems were formed in different structural levels. Foliation–parallel veins were precipitated beneath the seismogenic zone under pressure fluctuating from moderately sublithostatic to moderately subhydrostatic values (319–397 °C and 47–215 MPa), which is compatible with predicted fluid pressure cycle curves derived from fault–valve action. Growth of extensional veins occurred in shallower structural levels, under pressure fluctuating from near hydrostatic to moderately subhydrostatic values (207–218 °C and 18–74 MPa), which indicate that precipitation occurred within the near surface hydrostatically pressured seismogenic zone. Fluid immiscibility and precipitation of quartz in foliation–parallel veins resulted from fluid pressure drop immediately after earthquake rupture. Fluid immiscibility following a local pressure drop during extensional veining occurred in pre-seismic stages in response to the development of fracture porosity in the dilatant zone. Late stages of fluid circulation within the fault zone are represented dominantly by low to high salinity (0.2 to 44 wt.% equivalent NaCl) H2O–NaCl–CaCl2 fluid inclusions trapped in healed fractures mainly in foliation–parallel veins, which also exhibit subordinate H2O–NaCl–CaCl2, CO2–(CH4) and H2O–CO2–(CH4)–NaCl fluid inclusions trapped under subsolvus conditions in single healed microcracks. Recurrent circulation of aqueous–carbonic fluids and aqueous fluids of highly contrasting salinities during veining and post-veining stages suggests that fluids of different reservoirs were pumped to the ruptured fault zone during faulting episodes. A fluid evolution trending toward CH4 depletion for CO2–CH4–bearing fluids and salinity depletion and dilution (approximation of the system H2O–NaCl) for aqueous–saline fluids occurred concomitantly with decrease in temperature and pressure related to fluid entrapment in progressively shallower structural levels reflecting the shear zone exhumation history.  相似文献   

19.
The Kozbudaklar scheelite skarn deposit in the Tavşanlı Zone, located approximately 22 km southeast of Bursa, is hosted by the Triassic calcic İnönü Marble and Eocene Topuk Pluton. At least four stages have been recognized through skarn evolution. Scheelite skarn distributed close to the Topuk Pluton occurred during the early (stage 1) and late (stage 2) prograde substages. The early prograde endo and exoskarn are composed of hedenbergite (Hd96Joh4)–plagioclase (An55–64) and hedenbergite (Hd61–94Joh4–7), accompanied by calcic garnet (Grs38–94Sps1–5Alm0) and scheelite (Pow1–6). The second stage represents a relatively oxidized mineralogy dominated by diopside (Hd16–48Joh0–9), subcalcic garnet (Grs24–92Sps0–11Alm0–31) and scheelite (Pow7–32). The stage 3 and 4 mineral assemblages are characterized by few hydrous minerals in the retrograde stage and intense fracturing.Fluid inclusions from skarn rocks are indicative of multiple fluid events: (1) low-moderate salinity (5–16 wt.%NaCl equiv.) inclusions homogenized dominantly by a high-temperature (308 °C to > 600 °C) liquid phase in stage 1. Fluid inclusions in an early garnet homogenized over a similar temperature range (440 °C and 459 °C) into both liquid and vapor phases. Eutectic temperatures ranging from − 61.7 °C to − 35.0 °C that indicate the presence of H2O–NaCl–(± MgCl2 ± CaCl2)–CO2 solutions; (2) coexisting daughter mineral-bearing high salinity (29.5  70 wt.%NaCl equiv.) and vapor-rich moderate salinity (11.5–16.7 wt.%NaCl equiv.) inclusions that homogenized in the liquid phase by the disappearance of the vapor phase at a similar temperature range (308 °C to > 600 °C) in stage 2. Eutectic temperatures range from − 67.9°C to − 51.8°C that shows the presence of H2O–NaCl–CO2–(± CH4/N2) solutions; (3) low-moderate salinity (12.5–7.6 wt.%NaCl equiv.) and temperature (320 °C to 215 °C) inclusions homogenized by the liquid phase in stage 3. Eutectic temperatures range from − 59.5 °C to − 44.2 °C indicating the presence of H2O–NaCl–(± MgCl2 ± CaCl2)–CO2 solutions; (4) inclusions of low salinity (9.9–0.9 wt.%NaCl equiv.) and homogenization temperature (183 °C to 101 °C) in stage 4.These data show that the Kozbudaklar skarn deposit was formed in a magmatic–hydrothermal system. In this model, carbonaceous fluids may have been exsolved from the plutonic rock during its emplacement and crystallization. Fluid inclusion data indicate that fluid boiling and immiscibility occurred at temperatures between 440 °C and 459 °C and pressures ranging from 50 MPa to 60 MPa based on hydrostatic considerations. Early scheelite was precipitated with relatively reduced mineral compositions. As a result of depressurization, Mo-rich scheelite with oxidized minerals formed via high salinity and vapor-rich inclusions. The second scheelite mineralization occurred in a normal hydrothermal system by an infiltration mechanism at pressures between approximately 40 and 1.5 MPa. At shallow depths (< 1.5 MPa) with increasing permeability, sulfide and oxide minerals were deposited in the retrograde stage, greatly assisted by meteoric water. Finally, as a result of the diminishing of ore-forming fluids, post-depositional barren quartz and calcite veins were formed.  相似文献   

20.
Fluid inclusions that bear halite daughter minerals were discovered in volcanic rocks at Pingnan area in the Dongying sag. The samples of the fluid inclusions collected from the BGX-15 well drill cores are hosted in quartz of diorite-porphyrite. The daughter minerals are identified as NaCl crystals after being observed under a microscope and analyzed by in situ Raman spectroscopy at −185°C. The results of micro-thermal analysis show that the homogenization temperatures of primary fluid inclusions are between 359 and 496°C, and the salinities of fluid inclusions are from 43.26 to 54.51 wt-%. All fluid inclusions in the studied samples can be divided into five types including primary fluid inclusions and secondary fluid inclusions. The fact that five types of fluid inclusions were symbiotic in the same quartz grain implies that immiscibility happened in magma. Due to the decrease in temperature and pressure during the ascent of magma, the fluids became intensively immiscible. This process accelerates the degassing of CO2 from magma, but the remnant fluids with high salinity are preserved in fluid inclusions. Thus, the primary fluid inclusions are mainly in NaCl-H2O fluids and poor in CO2. The results of our study indicate that the degassing of magma and accumulation of CO2 gas at the Pingnan area are relative to the immiscibility of high salinity fluids. This discovery is important because it can help us have a further understanding of the mechanism of magma degassing and accumulation of the inorganic CO2 in eastern China. Translated from Acta Geologica Sinica, 2006, 80(11): 1699–1705 [译自: 地质学报]  相似文献   

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