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1.
We report carbonate- and silicate-rich globules and andradite from the Wajilitage kimberlitic rocks in the northwestern Tarim large igneous province, NW China. The carbonate-rich globules vary in size from 1 to 3 mm, and most have ellipsoidal or round shape, and are composed of nearly pure calcite. The silicate-rich globules are elliptical to round in shape and are typically larger than the carbonate-rich globules ranging from 2 to several centimeters in diameter. They are characterized by clear reaction rims and contain several silicate minerals such as garnet, diopside and phlogopite. The silicate-rich globules, reported here for the first time, are suggested to be related to the origin of andradite within the kimberlitic rocks. Our results show that calcite in the carbonate-rich globules has a high XCa (>0.97) and is characterized by extremely high concentrations of the total rare earth elements (up to 1500 ppm), enrichment in Sr (8521–10,645 ppm) and LREE, and remarkable depletion in Nd, Ta, Zr, Hf and Ti. The calcite in the silicate-rich globules is geochemically similar to those in the carbonate-rich globules except the lower trace element contents. Garnet is dominantly andradite (And59.56–92.32Grs5.67–36.03Pyr0.36–4.61Spe0–0.33) and is enriched in light rare earth elements (LREEs) and relatively depleted in Rb, Ba, Th, Pb, Sr, Zr and Hf. Phlogopite in the silicate-rich globules has a high Mg# ranging from 0.93 to 0.97. The composition of the diopside is Wo45.82–51.39En39.81–49.09Fs0.88–0.95 with a high Mg# ranging from 0.88 to 0.95. Diopside in the silicate-rich globules has low total rare earth element (REE) contents (14–31 ppm) and shows middle REE- (Eu to Gd), slight light REE- and heavy REE-enrichment with elevated Zr, Hf and Sr contents and a negative Nb anomaly in the normalized diagram. The matrix of the kimberlitic rocks are silica undersaturated (27.92–29.31 wt.% SiO2) with low Al2O3 (4.51–5.15 wt.%) and high CaO (17.29–17.77 wt.%) contents. The samples are characterized by incompatible element enrichment with high (La/Yb)N values (41–58) and remarkable negative anomalies in HFSEs (e.g. Ta, Zr, Hf). Our new data suggest that the carbonate-rich globule most likely crystallized at high-temperature and does not represent immiscible liquids, whereas the silicate-rich globules are related to carbonate-rich deuteric hydrothermal fluids during the later-stage of melt evolution. The fluids reacted with the surrounding silicate melts resulting in the formation of skarn minerals such as phlogopite, diopside and andradite. The presence of the carbonate-bearing globules indicates that the Wajilitage kimberlitic rocks are carbonate-rich and most likely derived from an enriched mantle with abundant carbonate. We correlate the carbonated mantle to metasomatism by the migration of deep-seated fluids (carbonate-rich) in response to the impingement of the early Permian mantle plume.  相似文献   

2.
In the Neoarchean (~ 2.7 Ga) contact metamorphosed charnockitic footwall of the Mesoproterosoic (1.1 Ga) South Kawishiwi intrusion of the Duluth Complex, the primary metamorphic mineral assemblage and Cu–Ni–PGE sulfide mineralization is overprinted by an actinolite + chlorite + cummingtonite + prehnite + pumpellyite + quartz + calcite hydrothermal mineral assemblage along 2–3 cm thick veins. In calcite, hosted by the hydrothermal alteration zones and in a single recrystallized quartz porphyroblast, four different fluid inclusion assemblages are documented; the composition of these fluid inclusions provide p–T conditions of the fluid flow, and helps to define the origin of the fluids and evaluate their role in the remobilization and reprecipitation of the primary metamorphic sulfide assemblage.Pure CO2 fluid inclusions were found as early inclusions in recrystallized quartz porphyroblast. These inclusions may have been trapped during the recrystallization of the quartz during the contact metamorphism of the footwall charnockite in the footwall of the SKI. The estimated trapping pressure (1.6–2.0 kbar) and temperature (810–920 °C) conditions correspond to estimates based on felsic veins in the basal zones of the South Kawishiwi intrusion.Fluid inclusion assemblages with CO2–H2O–NaCl and CH4–N2–H2O–NaCl compositions found in this study along healed microfractures in the recrystallized quartz porphyroblast establish the heterogeneous state of the fluids during entrapment. The estimated trapping pressure and temperature conditions (240–650 bar and 120–150 °C for CO2–H2O–NaCl inclusions and 315–360 bar and 145–165 °C for CH4–N2–H2O–NaCl inclusions) are significantly lower than the p–T conditions (> 700 °C and 1.6–2 kbar) during the contact metamorphism, indicating that this fluid flow might not be related to the cooling of the Duluth Complex and its contact aureole. The presence of chalcopyrite inclusions in these fluid inclusions and in the trails of these fluid inclusion assemblages confirms that at least on local scale these fluids played a role in base metal remobilization. No evidences have been observed for PGE remobilization and transport in the samples. The source of the carbonic phase in the carbonic assemblages (CO2; CH4) could be the graphite, present in the metasedimentary hornfelsed inclusions in the basal zones of the South Kawishiwi intrusion.The hydrothermal veins in the charnockite can be characterized by an actinolite + cummingtonite + chlorite + prehnite + pumpellyite + calcite (I–II) + quartz mineral assemblage. Chlorite thermometry yields temperatures around 276–308 °C during the earliest phase of the fluid flow. In the late calcite (II) phase, high salinity (21.6–28.8 NaCl + CaCl2 equiv. wt.%), low temperature (90–160 °C), primary aqueous inclusions were found. Chalcopyrite (± sphalerite ± millerite), replacing and intersecting the early hydrothermal phases, are associated to the late calcite (II) phase. The composition of the formational fluids in the Canadian Shield is comparable with the composition of the studied fluid inclusions. This suggests that the composition of the fluids did not change in the past 2 Ga and base metal remobilization by formational fluids could have taken place any time after the formation of the South Kawishiwi intrusion.Sulfur isotope studies carried out on the primary metamorphic (δ34S = 7.4–8.9‰) and the hydrothermal sulfide mineral assemblage (δ34S = 5.5–5.7‰) proves, that during the hydrothermal fluid flow the primary metamorphic ores were remobilized.  相似文献   

3.
Pegmatitic and other felsic rock pockets and dike-like intrusions are abundant in the South Kawishiwi Intrusion of the Duluth Complex, including the basal, Cu–Ni–PGE mineralized units. These occurrences are found as pockets, pods or as veins and contain abundant accessory apatite and quartz. Quartz hosts primary fluid inclusions as well as silicate melt inclusions. Combined microthermometry and Raman spectroscopy helped to determine the bulk composition of primary fluid inclusions that are CO2-rich (95 mol%) and contain small amounts of H2O (4.5 mol%), CH4 (0.4 mol%) and trace N2, respectively. This combined technique also made it possible to measure total homogenization temperatures of the inclusions (Thtot = ~ 225 ± 10 °C), otherwise not detectable during microthermometry. Silicate melt inclusions have been quenched to produce homogeneous glasses corresponding to the original melt. Composition of the entrapped melt is granitoid, peraluminous and is very poor in mafic components. We interpret the melt as a product of partial melting of the footwall rocks due to the contact effect of the South Kawishiwi Intrusion. The presence of CO2 in the vapor bubbles of the quenched melt inclusions and petrographic evidence suggest that the fluid and melt inclusion assemblages are coeval. The composition of the fluid and melt phase implies that the fluid originates from the mafic magma of the South Kawishiwi Intrusion and the fluid and melt phases coexisted as a heterogeneous melt–fluid system until entrapment of the inclusions.Coexistence of primary fluid and melt inclusions makes it possible to calculate a minimum entrapment pressure (~ 1.7 kbar) and thus estimate formation depth (~ 5.8 km) for the inclusions. Chlorine is suggested to behave compatibly in the silicate melt phase in the fluid–melt system represented by the inclusions, indicated by the high (up to 0.3%) Cl-concentrations of the silicate melt and CO2-rich nature of the fluid.Apatite halogen-contents provide further details on the behavior of Cl. Apatite in pegmatitic pockets often has elevated Cl-concentrations compared to troctolitic rocks, suggesting enrichment of Cl with progressive crystallization. Systematic trends of Cl-loss at some differentiated melt pockets suggest that in some places Cl exsolved into a fluid phase and migrated away from its source. The segregation of Cl from the melt is probably inhibited by the presence of CO2-rich fluids until the last stages of crystallization, increasing the potential for the development of late-stage saline brines.Platinum-group minerals are often present in microcracks in silicate minerals, in late-stage differentiated sulfide veinlets and in association with chlorapatite, indicating the potential role of Cl-bearing fluids in the final distribution of PGEs.  相似文献   

4.
The main effect of magma–carbonate interaction on magma differentiation is the formation of a silica-undersaturated, alkali-rich residual melt. Such a desilication process was explained as the progressive dissolution of CaCO3 in melt by consumption of SiO2 and MgO to form diopside sensu stricto. Magma chambers emplaced in carbonate substrata, however, are generally associated with magmatic skarns containing clinopyroxene with a high Ca-Tschermak activity in their paragenesis. Data are presented from magma–carbonate interaction experiments, demonstrating that carbonate assimilation is a complex process involving more components than so far assumed. Experimental results show that, during carbonate assimilation, a diopside–hedenbergite–Ca-Tschermak clinopyroxene solid solution is formed and that Ca-Tschermak/diopside and hedenbergite/diopside ratios increase as a function of the progressive carbonate assimilation. Accordingly, carbonate assimilation reaction should be written as follows, taking into account all the involved magmatic components:CaCO3solid + SiO2melt + MgOmelt + FeOmelt + Al2O3melt → (Di–Hd–CaTs)sssolid + CO2fluidThe texture of experimental products demonstrates that carbonate assimilation produces three-phases (solid, melt, and fluid) whose main products are: i) diopside–hedenbergite–Ca-Tschermak clinopyroxene solid solution; ii) silica-undersaturated CaO-rich melt; and iii) C–O–H fluid phase. The silica undersaturation of the melt and, more importantly, the occurrence of a CO2-rich fluid phase, must be taken into account as they significantly affect partition coefficients and the redox state of carbonated systems, respectively.  相似文献   

5.
Dikes of biotitic shonkinites and minettes of the complex Ryabinovyi alkaline massif (Central Aldan) have been studied. The dikes are localized in a neck of K-picrites in the northeast of the massif, which intrudes gold-bearing microcline–muscovite metasomatites (Muscovitovyi site). The obtained data on the chemical and trace-element compositions of the rocks and minerals and study of melt inclusions in clinopyroxenes indicate that the biotitic shonkinites and minettes crystallized from the same deep-seated high-pressure alkaline ultrabasic magma during its evolution. Apparently, at the early stage of crystallization of diopside in the biotitic shonkinites, homogeneous carbonate–silicate melt was separated into immiscible fractions of silicate, carbonate–salt, and carbonate melts. The temperature of melt immiscibility was > 1120–1190 °C, i.e., higher than the homogenization temperature of silicate inclusions in the diopside. The contents of trace elements in the biotitic shonkinites and rock-forming clinopyroxenes were one or two orders of magnitude higher than the mantle values. The Eu/Eu* ratios of both the considered rocks and the clinopyroxenes were close to those of chondrites, which testifies to their crystallization from mantle magma. The HREE/LREE ratio indicates that the magma source was localized at the depths where garnet-spinel assemblages existed. The negative Nb and Ti anomalies in the trace-element spectra and the high (> 5) La/Nb ratios in the rocks and clinopyroxenes point to the influence of crustal material on the parental magma. Crystallization of magma took place in reducing conditions, which is evidenced by the low (4–7) Ti/V ratios in clinopyroxenes and the presence of chloride–sulfate inclusions in them. Since gold in the Ryabinovyi massif is associated with late sulfate–chloride and sulfate–carbonate fluids, it might have been transported by alkaline chloride–sulfate and carbonate (carbonatite) melts, found as inclusions in clinopyroxenes of the biotitic shonkinites, at the early stages of Mesozoic magmatism.  相似文献   

6.
The Huijiabao gold district is one of the major producers for Carlin-type gold deposits in southwestern Guizhou Province, China, including Taipingdong, Zimudang, Shuiyindong, Bojitian and other gold deposits/occurrences. Petrographic observation, microthermometric study and Laser Raman spectroscopy were carried out on the fluid inclusions within representative minerals in various mineralization stages from these four gold deposits. Five types of fluid inclusions have been recognized in hydrothermal minerals of different ore-forming stages: aqueous inclusions, CO2 inclusions, CO2–H2O inclusions, hydrocarbon inclusions, and hydrocarbon–H2O inclusions. The ore-forming fluids are characterized by a H2O + CO2 + CH4 ± N2 system with medium to low temperature and low salinity. From early mineralization stage to later ones, the compositions of the ore-forming fluids experienced an evolution of H2O + NaCl → H2O + NaCl + CO2 + CH4 ± N2 → H2O + NaCl ± CH4 ± CO2 with a slight decrease in homogenization temperature and salinity. The δ18O values of the main-stage quartz vary from 15.2‰ to 24.1‰, while the δDH2O and calculated δ18OH2O values of the ore-forming fluids range from −56.9 to −116.3‰ and from 2.12‰ to 12.7‰, respectively. The δ13CPDB and δ18OSMOW values of hydrothermal calcite change in the range of −9.1‰ to −0.5‰ and 11.1–23.2‰, respectively. Stable isotopic characteristics indicate that the ore-forming fluid was mainly composed of ore- and hydrocarbon-bearing basinal fluid. The dynamic fractionation of the sulfur in the diagenetic pyrite is controlled by bacterial reduction of marine sulfates. The hydrothermal sulfides and the diagenetic pyrite from the host rocks are very similar in their sulfur isotopic composition, suggesting that the sulfur in the ore-forming fluids was mainly derived from dissolution of diagenetic pyrite. The study of fluid inclusions indicates that immiscibility of H2O–NaCl–CO2 fluids took place during the main mineralization stage and caused the precipitation and enrichment of gold.  相似文献   

7.
Granitic leucosome and pegmatite are widely distributed within biotite-bearing orthogneiss in the northern part of the Sulu ultrahigh-pressure (UHP) metamorphic terrane, eastern China. A combined study of mineral inclusions, cathodoluminescence (CL) images, U–Pb SHRIMP dates, and in situ trace element and Lu–Hf isotope analyses of zircons provided insight into the nature and timing of partial melting in these rocks. Zircon grains separated from biotite-bearing orthogneiss typically have three distinct domains: (1) pre-metamorphic (magmatic) cores with Qtz + Kfs + Pl + Ap inclusions, which record a Neoproterozoic protolith age of ～ 790 Ma, (2) mantles with Coe + Phe + Ap inclusions that record Triassic UHP age at 227 ± 3 Ma, and (3) narrow rims with quartz inclusions that record HP granulite-facies retrograde metamorphism at ～ 210 ± 3 Ma. In contrast, zircons separated from granitic leucosome have only two distinct domains: (1) the central UHP areas with Coe + Phe + Ap inclusions record Triassic UHP age of 227 ± 3 Ma, and (2) outer magmatic areas with Qtz + Kfs + Ab + Ap inclusions that record partial melting time of 212 ± 2 Ma. Zircons separated from pegmatite contain mineral inclusions of Qtz + Kfs + Ap and show regular magmatic zoning from centre to edge. The centres record partial melting time of 212 ± 2 Ma in line with the outer domains of granitic leucosome, whereas the edges give a younger age of 201 ± 2 Ma related to Pb loss and partial recrystallization during late Triassic regional amphibolite-facies retrogression. These data indicate that partial melting in the north Sulu UHP gneissic rocks took place during post-UHP, retrograde HP granulite-facies metamorphism.Pre-metamorphic (magmatic) zircon cores from biotite-bearing orthogneiss give uniform 176Hf/177Hf of 0.28187 ± 0.00003 (2 SD; standard deviation) corresponding to εHf(790) and Hf model ages (TDM2) of about ? 16.3 and 2.41 Ga, respectively. This is consistent with the generation of its protolith by reworking of Paleoproterozoic to late Archean crust. In contrast, UHP zircon domains from biotite-bearing orthogneiss and granitic leucosome are characterized by distinct trace element composition with low Lu/Hf (< 0.006), low Th/U (< 0.1) and considerably higher, 176Hf/177Hf (0.28233 ± 0.00002; 2 SD) than the pre-metamorphic cores. The uniform but significantly different Hf isotope composition between the UHP (εHf(227) = ? 14.6 ± 0.8; 2 SD) and pre-metamorphic (εHf(227) = ? 27.7) domains indicates equilibration of the Lu–Hf isotope system only within the UHP metamorphic mineral assemblage. The disequilibrium between whole rock and UHP zircon suggests that about two thirds of the whole rock Hf retained in the pre-metamorphic zircon domains. Zircon domains crystallized during partial melting at 212 Ma in granitic leucosome and pegmatites have a Hf isotope composition indistinguishable from that of the UHP zircon domains. This suggests that only Hf (and Zr) equilibrated during UHP metamorphism was remobilized during partial melting while pre-metamorphic zircon remained stable or was not accessible. In contrast, the magmatic zircon edges from pegmatite have somewhat lower 176Hf/177Hf (～ 0.28216) and εHf(t) (? 17.6 ± 1.2; 2 SD) indicating some release of less radiogenic Hf for instance by dissolution of pre-metamorphic zircon during late regional amphibolite-facies retrogression.  相似文献   

8.
The large Yueyang Ag-Au-Cu deposit is commonly regarded as a low-sulfidation epithermal deposit in the Zijinshan orefield, Fujian Province, southeastern China. The Ag-Ag-Cu orebodies hosted in the Zijinshan granitic batholith are mainly stratoid and lens in shape, and controlled by a series of NW-trending listric faults with shallow dip angles. Four mineralization stages are recognized on the basis of mineral assemblage, ore fabrics, and crosscutting relationships of the ore veins, namely: pre-ore (pyrite + sericite + quartz ± chlorite), main Cu (chalcopyrite + pyrite + sericite + quartz ± bornite), main Ag-Au (Ag and Au minerals + pyrite + quartz + adularia ± calcite ± apatite ± chalcopyrite ± galena ± sphalerite) and post-ore (quartz ± chalcedony ± calcite) stages. Fluid inclusions (FIs) in the deposit include aqueous liquid-rich (WL-), aqueous vapor-rich (WV-), and minor carbonic (C-) and daughter mineral-bearing (S-) type ones. WL-subtype is the main inclusion type in the Yueyang deposit, accounting for more than 90% in proportion in each stage. Minor WV-subtype inclusions occur in both the main Cu and Ag stages, while the C-type and S-type ones are only observed in the main Cu stage. Fluid inclusion and H-O isotope study indicated that the ore-forming fluid of the main Cu stage is primarily magmatic vapor, which further underwent fluid boiling and mixing with meteoric water, while the ore-forming fluid of the main Ag stage is meteoric water-dominated, and the precipitation of silver and gold was mainly resulted from fluid boiling and the precipitation of other sulfides. On the basis of the aforementioned geological, fluid inclusion and stable isotope studies, we proposed a two-stage model for the Yueyang deposit, including a magmatic vapor-related porphyry type Cu mineralization and meteoric water-related low-sulfidation epithermal Ag-Au-Cu mineralization, although the porphyry Cu mineralization is very limited in scale. The mineralization and exhumation depths of the Yueyang deposit are estimated to be 448‒527 m and 18‒97 m, respectively. By comparison with the exhumation depths of other deposits in the Zijinshan orefield, it is suggested that more epithermal deposits could be found in the southwest of the orefield due to less uplift and exhumation therein.  相似文献   

9.
《Lithos》2007,93(1-2):68-88
In the Eclogite Zone of the Tauern Window, a layer of strongly retrogressed leucocratic jadeite-bearing gneiss is intercalated between mafic kyanite-eclogites. The jadeite-gneiss consists of garnet + quartz + paragonite ± phengite ± zoisite + zircon + rutile + apatite + pyrite. Kyanite, jadeite or omphacite are exclusively present as inclusions in garnet. Retrogressive hydration during exhumation led to a breakdown of matrix jadeite to form pseudomorphs of calcic amphibole + albite. Peak metamorphic conditions derived from the primary gneiss assemblage are 2.0–2.4 GPa at approximately 640 °C. Major, trace element and isotopic compositions of the jadeite-gneiss are consistent with a siliciclastic sedimentary protolith. Zircon morphology and zonation patterns reveal a complex history. The presence of fracture-truncated zircons suggests a detrital origin, whereas most internal structures and Th/U ratios are characteristic of zircons from magmatic rocks. In situ LA-ICP-MS and SHRIMP U–Pb geochronology and zircon geochemisty provide evidence of at least three magmatic events in the provenance area. These were dated at 466 ± 2 Ma, 437 ± 2 Ma and 288 ± 9 Ma. Older ages ranging from 503 to 691 Ma are preserved in the cores of some zircon grains, suggesting derivation from peri-Gondwanan sources. Surprisingly, no firm evidence of the Tertiary high-pressure metamorphic event and subsequent retrograde overprint was seen in any of the studied zircons. However, some zircons show resorbed surfaces suggesting corrosion by a superficial fluid phase undersaturated in zirconium and one extensively altered porous zircon yielded highly discordant 206Pb/238U ages in the range 325–109 Ma documenting partial recrystallization by dissolution–reprecipitation of a highly reactive grain.  相似文献   

10.
The effect of fluorine on the solubilities of Mn-columbite (MnNb2O6), Mn-tantalite (MnTa2O6), zircon (ZrSiO4) and hafnon (HfSiO4) were determined in highly fluxed, water-saturated haplogranitic melts at 800 to 1000 °C and 2 kbar. The melt composition corresponds to the intersection of the granite minimum with the albite–orthoclase tieline (Ab72Or28) in the quartz–albite–orthoclase system (Q–Ab–Or), which is representative of a highly fluxed melt, from which high field strength element minerals may crystallize. The melt contains 1.7 wt.% P2O5, 1.05 wt.% Li2O and 1.83 wt.% B2O3. The main purpose of this study is to examine the effect of F on columbite, tantalite, zircon and hafnon solubility for a melt with this composition. Up to 6 wt.% fluorine was added as AgF in order to keep the aluminum saturation index (ASI, molar Al/[Na + K]) of the melt constant. In an additional experiment F was added as AlF3 to make a glass peraluminous. The nominal ASI of the melts are close to 1 for the minimum composition and approximately 1.32 in peraluminous glasses, but if Li is considered as an alkali, the molar ratio Al/[Na + K + Li] of the melts are alkaline (0.87) and subaluminous (1.09), respectively.The molar solubility products [MnO] 1 [Nb2O5] and [MnO] 1 [Ta2O5] are nearly independent of the F content of the melt, at approximately 18.19 ± 1.2 and 43.65 ± 2.5 × 10− 4 (mol2/kg2), respectively for the minimum composition. By contrast, there is a positive dependence of zircon and hafnon solubilities on the fluorine content in the minimum composition, which increases from 2.03 ± 0.03 × 10− 4 (mol/kg) ZrO2 and 4.04 ± 0.2 × 10− 4 (mol/kg) HfO2 for melts with 0 wt.% F to 3.81 ± 0.3 × 10− 4 (mol/kg) ZrO2 and 6.18 ± 0.04 × 10− 4 (mol/kg) HfO2 for melts with 8 wt.% F. Comparison of the data from this work and previous studies indicates that ASI of the melt seems to have a stronger effect than the contents of fluxing elements in the melt and the overall conclusion is that fluorine is less important (relative to melt compositions) than previously thought for the control on the behavior of high field strength elements in highly evolved granitic melts. Moreover, this study confirms that although Nb, Ta, Zr and Hf are all high field strength elements, Nb–Ta and Zr–Hf are complexed differently in the melt.  相似文献   

11.
Peridotite mantle xenoliths collected north of Gobernador Gregores, Patagonia, affected by cryptic and modal metasomatism bear melt pockets of unusually large size. Melt pockets consist of second generation olivine (ol2), clinopyroxene (cpx2) and spinel (sp2) ± relict amphibole (amph) immersed in a yellowish vesicular glass matrix. Amphibole breakdown was responsible for melt pocket generation as suggested by textural evidence and proved by consistent mass-balance calculations: amph → cpx2 + ol2 + sp2 + melt. Composition of calculated amphibole in amphibole-free melt pockets is very similar to that measured in amphibole-bearing melt pockets from the same xenolith, i.e. amphibole was consumed in the melt pocket generation process. In melt pockets devoid of relict amphibole, mass-balance calculations show remarkable differences between the calculated amphibole and the measured amphibole compositions in melt pockets from the same xenolith. The participation of minor proportions of a consumed reactant phase could be a reasonable explanation. In some samples the calculated phase proportion of glass is in excess compared to modal estimations based on backscattered electron images, probably because a portion of the generated melt was able to migrate out of the melt pockets. Compositional inhomogeneity of cpx2 and variable Ti Kd in cpx2 vs. glass in the same melt pocket reflect fast nucleation and growth and disequilibrium crystallisation, respectively. This and the difference between forsterite content in calculated equilibrium olivine and second generation olivine, suggest that mineral equilibrium was inhibited by rapid quenching of melt pockets.  相似文献   

12.
The Huangshannan Ni–Cu sulfide deposit at the southern margin of the Central Asian Orogenic Belt (CAOB) is an important recent discovery in the Eastern Tianshan Region, Northwestern China. The Huangshannan Intrusion is composed of mafic and ultramafic rocks, and its websterite and lherzolite sequences host the sulfide orebodies. Olivine is the dominant mineral in the Huangshannan Intrusion, occurring as olivine inclusions hosted by pyroxene oikocrysts, as olivine crystals in magmatic sulfides, and as poikilitic crystals in the lherzolite. Small olivine inclusions always coexist with large poikilitic olivine crystals in the same sample, resulting in a heterogeneous texture on the scale of the oikocrysts. The Ni abundance ranges from 1540 to 3772 ppm in poikilitic olivine grains, from 2114 to 3740 ppm in olivine grains hosted by sulfide minerals, and from 2043 to 4023 ppm in olivine inclusions hosted by pyroxene oikocrysts. For the three types of olivine, the ranges in forsterite (Fo) content are 78.97–84.92 mol.%, 81.57–84.79 mol.%, and 80.33–84.68 mol.%, respectively. The Ni content of olivine in the lherzolite is anomalously high relative to the range found in most within plate olivine-bearing mafic-ultramafic rocks. The composition of olivine is controlled mainly by that of the parental magma, fractional crystallization and reactions with interstitial silicate and sulfide melts. Both fractional crystallization and reaction with interstitial silicate may cause a decrease in the Ni content of olivine. The possibility that Ni–Fe exchange causes the anomalously high Ni contents in olivine can be excluded because the olivine grains contained in sulfide have similar or lower Ni content than the olivine grains hosted in the silicate rock. Most of the olivine grains are unzoned, and they have anomalously high Ni contents throughout the crystal. Assuming a partition coefficient of Ni between olivine and silicate magma to be 7, the measured Ni content of olivine in the lherzolite (1540–4023 ppm with a mean of 2907 ppm) indicates that the parental magma contains 220–575 ppm (average of 415 ppm) Ni. This value is higher than that found in basaltic magmas that crystallized olivine with similar Fo contents compared to the Huangshannan Intrusion. As mentioned above, the symmetric and reproducible variations in both Fo and Ni contents from core to margin in most of the olivine grains cannot be explained by fractional crystallization and reactions with interstitial silicate or sulfide melts but may reflect the equilibration of the olivine with new fluxes of magma as the chamber was replenished. The anomalously Ni-rich composition of the parental magmas of the Huangshannan Intrusion, relative to those of many other mineralized olivine-bearing mafic-ultramafic intrusions, may be produced by upgrading and scavenging of metals from a previously formed sulfide melts by a moderately Ni-rich magma. The mass-balance calculations of PGE data indicate that the parental magma that formed lherzolite contains 0.04 ppb Os, 0.02 ppb Ir and 0.4 ppb Pd, whereas the parental magma that formed websterite has 0.02 ppb Os, 0.009 ppb Ir and 0.75 ppb Pd. Rayleigh modeling using PGE tenors indicates that the massive sulfides may be produced by monosulfide solid solution (MSS)-sulfide liquid fractionation from the magma that formed the websterite. Rayleigh modeling of Fo and Ni contents of olivine shows that the parental magma that formed the lherzolite has experienced previous sulfide segregation and olivine crystallization.  相似文献   

13.
We investigated several mineral phases and their replacement products which occur as inclusions in garnets from felsic and mafic granulites of the Gföhl Unit in the Moldanubian Zone. The most important mineral inclusions, Ti-rich muscovite and omphacite, were used for the reconstruction of the metamorphic history of granulites. Some inclusions were transformed during high-temperature granulite facies metamorphism, partial melting and decompression to other phases, and so the original mineral can only be deduced from the inclusion morphology and reaction products. These inclusions have columnar shapes and consist of K-feldspar + kaolinite, albite + Fe-oxide, plagioclase + Fe-oxide, or albite + K-feldspar, respectively. The pseudomorphs with albite/plagioclase occur in a Ca-rich garnet that shows prograde zoning. Pressure–temperature (PT) evolution, derived from mineral assemblages in granulite and based on the inclusions, suggests a prograde metamorphism from amphibolite through eclogite to granulite facies conditions with subsequent amphibolite facies overprint during exhumation. The estimated PT trajectory for the studied granulites, which also host lenses or boudins of eclogites and garnet peridotites, allows reconstruction of the complete clockwise metamorphic path that is consistent with subduction geotherm prior to the tectonic amalgamation within the continental collisional root.  相似文献   

14.
The Luoboling Cu–Mo deposit in the Zijinshan Orefield, Fujian province, southeastern China, is a large porphyry deposit hosted by the Sifang granodiorite and the Luoboling granodiorite porphyry. The largest Cu–Mo orebody is saddle-shaped with various types of hydrothermal veinlets. Intensive hydrothermal alteration in the deposit is characterized by outward zoning from potassic, overprinted by phyllic alteration, to phyllic and alunite–dickite alteration. Based on the mineral assemblages and crosscutting relationships of veins, the ore-forming process can be divided into three stages, namely: an early-stage K-feldspar + quartz ± magnetite ± molybdenite veins associated with potassic alteration; a middle-stage quartz + molybdenite + chalcopyrite + pyrite veins in phyllic zone; and a late-stage quartz ± gypsum veins in the phyllic and alunite–dickite alteration zones. Six molybdenite separates yield a Re−Os isochron age 104.6 ± 1.0 Ma, which is identical to the age of emplacement of the Sifang and Luoboling granodiorite porphyries. Three types of fluid inclusions (FIs) were observed at the Luoboling deposit: 1) NaCl–H2O (aqueous), 2) daughter mineral-bearing and 3) CO2–H2O fluid inclusions. FIs of the early and middle stages are predominantly vapor-rich aqueous and daughter mineral-bearing inclusions, together with minor CO2-rich and liquid-rich aqueous inclusions; whereas the late-stage minerals only contain liquid-rich aqueous inclusions. Homogenization temperatures and salinities of FIs trapped in the early-stage minerals range from 420 to 540 °C and 0.4 to 62.9 wt.% NaCl equiv., respectively. FIs of the middle-stage yield homogenization temperatures of 340 to 480 °C and salinities of 0.5 to 56.0 wt.% NaCl equiv. CO2 content and the oxygen fugacity (indicated by daughter minerals) of FIs trapped in middle-stage minerals are lower than those in the early stage. The liquid-rich aqueous inclusions of the late-stage homogenize at temperatures of 140 to 280 °C, yielding salinities of 0.4 to 8.4 wt.% NaCl equiv. The minimum estimated pressures of the three stages are 30–70 MPa, 10–40 MPa and 1–10 MPa, respectively, corresponding to minimum ore-forming depths of 1–2.8 km. Fluids trapped in early, middle and late stages yield δD values of − 67‰ to − 54‰, − 54‰ to − 70‰, and − 62‰, and δ18O values of 5.4‰ to 6.7‰, 2.8‰ to 4.2‰, and − 2.1‰, respectively. Fluid boiling, which resulted in the formation of stockworks and the precipitation of sulfides, occurred in the early and middle stages. The fluids subsequently evolved into a low temperature, low salinity system in the late stage, along with an input of meteoric water. The Luoboling porphyry Cu–Mo system was developed in a transition from continental arc to back-arc extension region, which was related to the westward subduction of the paleo-Pacific plate beneath the Huanan Orogen.  相似文献   

15.
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   

16.
《Lithos》2007,93(1-2):107-125
Sapphirine, spinel, orthoamphibole ± quartz and kyanite are included in porphyroblastic garnet in biotitic gneiss enclosed in a lens of metamorphosed ultramafic rocks in the Cambrian granulite-facies metamorphic complex of the eastern Sør Rondane Mountains, Queen Maud Land, East Antarctica. A bulk analysis of the biotitic gneiss reveals features characteristic both of ultramafic rocks, e.g., high contents of Cr and Ni, and of metasomatism associated with fluids having a crustal source, e.g., relatively elevated contents of Li, Rb, Mo, Cs, Ba, Tl, and Pb. This trace element signature is consistent with the biotitic gneiss being a slice of blackwall skarn that developed between harzburgite and the enclosing biotite–hornblende ± garnet ± orthopyroxene ± clinopyroxene gneiss and was subsequently infolded or inserted by faulting. The matrix assemblage of the biotitic gneiss is garnet + corundum + hercynite + biotite +plagioclase +allanite + zircon. The included associations (all with biotite and rutile) are (1) sapphirine + kyanite, (2) spinel + kyanite, (3) sapphirine +spinel, (4) kyanite, and (5) orthoamphibole + plagioclase ± quartz. The garnet porphyroblasts are compositionally zoned with broad pyropic cores (XMg(=Mg / (total Fe + Mg)) = 0.45–0.55) surrounded by Fe-richer rims (XMg ≈ 0.3 at the outermost part). The garnet cores preserve compositions homogenized under peak conditions of the granulite-facies metamorphism (760–800 °C and 7–8 kb), whereas the Fe-enriched rims are attributed to an amphibolite-facies overprint at 500–600 °C. Theoretical calculations of garnet + corundum + spinel ± sapphirine + kyanite equilibria in the FMAS system constrain possible P–T conditions for a sapphirine + spinel + kyanite + garnet (XMg ≈ 0.55) assemblage to form near 450 °C and 4 kb on the prograde path. In contrast, a modified calibration of the Das et al. (Das, K., Fujino, K., Tomioka, N., Miura, H., 2006. Experimental data on Fe and Mg partitioning between coexisting sapphirine and spinel: an empirical geothermometer and its application. Eur. J. Mineral., 18, 49–58). sapphirine–spinel thermometer gives 860–895 °C for the included associations; pressures would have to be at least 12 kb to stabilize kyanite at these temperatures. Neither estimate is satisfactory and the stability range of kyanite + spinel–hercynite ± sapphirine assemblages remains an unresolved question. The Sør Rondane Mountains constitute the third region for kyanite, sapphirine and spinel–hercynite inclusions in garnet in granulite-facies rocks of the Neoproterozoic–Cambrian orogen extending from the Sør Rondane Mountains to Lützow–Holm Bay and onward to Sri Lanka, southern India and southern Madagascar, and thus determining the stability range of kyanite + spinel–hercynite ± sapphirine is critical for deducing the tectonic evolution of this orogen.  相似文献   

17.
The Jiama deposit, located in the eastern part of the well-known Gangdese Metallogenic Belt on the Tibetan Plateau, is the largest porphyry Cu–polymetallic system in the region, with the largest exploration budget, and is economically viable in the Gangdese Belt to undergo large-scale development. The deposit is well preserved and has experienced little erosion. The proven resources of the deposit are 7.4 Mt Cu, 0.6 Mt Mo, 1.8 Mt Pb + Zn, 6.65 Moz Au, and 360.32 Moz Ag. The results presented in this paper are based on geological and tectonic mapping, geological logging, and other exploration work performed by members of the Jiama Exploration Project Team over a period of 6 years. We propose that the Jiama porphyry Cu–polymetallic system is composed of skarn Cu–polymetallic, hornfels Cu–Mo, porphyry Mo ± Cu, and distal Au mineralization. The development of skarn Cu–polymetallic orebodies at the Jiama deposit was controlled mainly by the contact zone between porphyries and marbles, an interlayer detachment zone, and the front zone of a gliding nappe structure. The hornfels Cu–Mo and porphyry Mo ± Cu orebodies were controlled mainly by a fracture system related to intrusions, and the distal Au mineralization resulted from late-stage hydrothermal alteration.On the basis of field geological logging, optical microscopy, and chemical analysis, we verify that the alteration zones in the Jiama deposit include potassic, phyllic, propylitic, and argillic alteration, with a local lithocap, as well as endoskarn and exoskarn zones. The endoskarn occurs mainly as epidote alteration in quartz diorite porphyry and granite porphyry, and is cut by massive andradite veins. The exoskarn includes garnet–pyroxene and wollastonite skarn, in which the mineralogy and mineral chemical compositions display an outward zonation with respect to the source porphyry. From the proximal skarn to the intermediate skarn to the distal skarn, the garnet/pyroxene ratio varies from > 20:1 to ~ 10:1 to ~ 5:1, the garnet color varies from red-brown to brown-green to green-yellow, and the average composition of garnet varies from Ad80.1Gr18.9(Sp + Py)1.0 to Ad76.3Gr23(Sp + Py)0.7 to Ad59.5Gr39.5(Sp + Py)1.0, respectively. The pyroxene is not as variable in composition as the garnet, and is primarily light green to white diopside with a maximum hedenbergite content of ~ 20% and an average composition of Di88.6Hd8.9Jo2.5. From the proximal skarn to the intermediate skarn to the distal skarn, the mineralization changes from Cu–Mo to Cu ± Mo to Pb–Zn ± Cu ± Au ores, respectively. The wollastonite skarn displays no zonation and hosts mainly bornite mineralization. The Cu and Mo mineralization is closely related to the potassic and phyllic zones in the porphyry–hornfels.Zircons from four mineralized porphyries yield U–Pb ages of 15.96 ± 0.5 Ma, 15.72 ± 0.14 Ma, 15.59 ± 0.09 Ma, and 15.48 ± 0.08 Ma. The Re–Os ages of molybdenite from the skarn, hornfels, and porphyry are 15.37 ± 0.15 Ma, 14.67 ± 0.37 Ma, and 14.66 ± 0.27 Ma, respectively. The present results are consistent with the findings of previous research on fluid inclusions, isotopes, and other such aspects. On the basis of the combined evidence, we propose a porphyry Cu–polymetallic system model for the Jiama deposit and suggest a regional exploration strategy that can be applied to prospecting for porphyry-skarn mineralization in the Lhasa area.  相似文献   

18.
The precise constraints on the timing of metamorphism of the Changhai metamorphic complex is of great importance considering the prolonged controversial issue of the north margin and the extension of the Sulu–Dabie HP–UHP Belt. While the monazite U–Th–Pb and muscovite 40Ar/39Ar techniques are widely accepted as two of the most powerful dating tools for revealing the thermal histories of medium–low grade metamorphic rocks and precisely constraining the timing of metamorphism. The Changhai metamorphic complex at the SE Jiao–Liao–Ji Belt, North China Craton consists of a variety of pelitic schist and Grt–Ky-bearing paragneiss, and minor quartzite and marble. Analyses of mineral inclusions and back-scattered electric (BSE) images of monazites, combined with LA–ICP–MS U–Th–Pb ages for monazites and 40Ar/39Ar ages for muscovites, provide evidence of the origin and metamorphic age of the Changhai metamorphic complex. Monazites separates from various Grt–Mus schists and Grt–Ky–St–Mus paragneisses exhibit homogeneous BSE images from cores to rims, and contain inclusion assemblages of Grt + Mus + Qtz ± Ctd ± Ky in schist, and Grt + Ky + St + Mus + Pl + Kfs + Qtz inclusions in paragneiss. These inclusion assemblages are very similar to matrix minerals of host rocks, indicating they are metamorphic rather than inherited or detrital in origin. LA–ICP–MS U–Th–Pb dating reveals that monazites of schist and paragneiss have consistent 206Pb/238U ages ranging from 228.1 ± 3.8 to 218.2 ± 3.7 Ma. In contrast, muscovites from various schists show slightly older 40Ar/39Ar plateau ages of 236.1 ± 1.5 to 230.2 ± 1.2 Ma. These geochronological and petrological data conclude that the pelitic sediments have experienced a metamorphic event at the Mid–Late Triassic (236.1–218.2 Ma) rather than the Paleoproterozoic (1950–1850 Ma), commonly regarded as the Precambrian basement for the Jiao–Liao–Ji Belt. Hence, the Changhai metamorphic complex should be considered as a discrete lithotectonic group.This newly recognized Mid–Late Triassic metamorphic event (236.1–218.2 Ma) for the Changhai metamorphic complex is coeval with the HP–UHP metamorphic event (235–220 Ma) for Sulu–Dabie rocks. This leads us to speculate that the metamorphism of the Changhai complex belt along the SE margin of the North China Craton was genetically related to the Mid–Late Triassic collision of the North China and South China cratons. By the same token, the Sulu–Dabie HP–UHP Belt may have extended through Yantai, and the southern Yellow Sea, and to the southern side of the Changhai metamorphic complex.  相似文献   

19.
《Lithos》2007,93(1-2):175-198
The Neoproterozoic (∼ 820 Ma) Aries micaceous kimberlite intrudes the central Kimberley Basin, northern Western Australia, and has yielded a suite of 27 serpentinised ultramafic xenoliths, including spinel-bearing and rare, metasomatised, phlogopite–biotite and rutile-bearing types, along with minor granite xenoliths. Proton-microprobe trace-element analysis of pyrope and chromian spinel grains derived from heavy mineral concentrates from the kimberlite has been used to define a ∼ 35–40 mW/m2 Proterozoic geotherm for the central Kimberley Craton. Lherzolitic chromian pyrope highly depleted in Zr and Y, and Cr-rich magnesiochromite xenocrysts (class 1), probably were derived from depleted garnet peridotite mantle at ∼ 150 km depth. Sampling of shallower levels of the lithospheric mantle by kimberlite magmas in the north and north-extension lobes entrained high-Fe chromite xenocrysts (class 2), and aluminous spinel-bearing xenoliths, where both spinel compositions are anomalously Fe-rich for spinels from mantle xenoliths. This Fe-enrichment may have resulted from Fe–Mg exchange with olivine during slow cooling of the peridotite host rocks. Fine exsolution rods of aluminous spinel in diopside and zircon in rutile grains in spinel- and rutile-bearing serpentinised ultramafic xenoliths, respectively, suggest nearly isobaric cooling of host rocks in the lithospheric mantle, and indicate that at least some aluminous spinel in spinel-facies peridotites formed through exsolution from chromian diopside. Fe–Ti-rich metasomatism in the spinel-facies Kimberley mantle probably produced high-Ti phlogopite–biotite + rutile and Ti, V, Zn, Ni-enriched aluminous spinel ± ilmenite associations in several ultramafic xenoliths. U–Pb SHRIMP 207Pb/206Pb zircon ages for one granite (1851 ± 10 Ma) and two serpentinised ultramafic xenoliths (1845 ± 30 Ma; 1861 ± 31 Ma) indicate that the granitic basement and lower crust beneath the central Kimberley Basin are at least Palaeoproterozoic in age. However, Hf-isotope analyses of the zircons in the ultramafic xenoliths suggest that the underlying lithospheric mantle is at least late Archean in age.  相似文献   

20.
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   

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