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1.
Implication of Apatite and Anhydrite for Formation of an Iron‐Oxide‐Apatite (IOA) Rare Earth Element Prospect,Benjamin River,Canada 
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下载免费PDF全文 The Benjamin River apatite prospect in northern New Brunswick, Canada, is hosted by the Late Silurian Dickie Brook plutonic complex, which is made up of intrusive units represented by monzogranite, diorite and gabbro. The IOA ores, composed mainly of apatite, augite, and magnetite at Benjamin River form pegmatitic pods and lenses in the host igneous rocks, the largest of which is 100 m long and 10–20 m wide in the diorite and gabbro units. In this study, 28 IOA ore and rock samples were collected from the diorite and gabbro units. Mineralogical observations show that the apatite–augite–magnetite ores are variable in the amounts of apatite, augite, and magnetite and are associated with minor amounts of epidote‐group minerals (allanite, REE‐rich epidote and epidte) and trace amounts of albite, titanite, ilmenite, titanomagnetite, pyrite, chlorite, calcite, and quartz. Apatite and augite grains contain small anhydrite inclusions. This suggests that the magma that crystallized apatite and augite had high oxygen fugacity. In back scattered electron (BSE) images, apatite grains in the ores have two zones of different appearance: (i) primary REE‐rich zone; and (ii) porous REE‐poor zone. The porous REE‐poor zones mainly appear in rims and/or inside of the apatite grains, in addition to the presence of apatite grains which totally consist of a porous REE‐poor apatite. This porous REE‐poor apatite is characterized by low REE (<0.84 wt%), Si (<0.28 wt%), and Cl (<0.17 wt%) contents. Epidote‐group minerals mainly occur in grain boundary between the porous REE‐poor apatite and augite. These indicate that REE leached from primary REE‐rich apatite crystallized as allanite and REE‐rich epidote. Magnetite in the ores often occurs as veinlets that cut apatite grains or as anhedral grains that replace a part of augite. These textures suggest that magnetite crystallized in the late stage. Pyrite veins occur in the ores, including a large amount of quartz and calcite veins. Pyrite veins mainly occur with quartz veins in augite. These textures indicate pyrite veins are the latest phase. Apatite–augite–magnetite ore, gabbro–quartz diorite and feldspar dike collected from the Benjamin River prospect contain dirty pure albite (Ab98Or2–Ab100) under the microscope. The feldspar dikes mainly consist of dirty pure albite. Occurrences of the dirty pure albite suggest remarkable albitization (sodic alteration) of original plagioclase (An25.3–An60 in Pilote et al., 2012) associating with intrusion of monzogranite into gabbro and diorite. SO42? bearing magma crystallized primary REE‐rich apatite, augite and anhydrite reacted with Fe in the sodic fluids, which result in oxidation of Fe2+ and release of S2? into the sodic fluids. REE, Ca and Fe from primary REE‐rich apatite, augite and plagioclase altered by the sodic fluids were released into the fluids. Then Fe3+ in the sodic fluids precipitated as Fe oxides and epidote‐group minerals in apatite–augite–magnetite ores. Finally, residual S2? in sodic fluids crystallized as latest pyrite veins. In conclusion, mineralization in Benjamin River IOA prospect are divided into four stages: (1) oxidized magmatic stage that crystallized apatite, augite and anhydrite; (2) sodic metasomatic stage accompanying alteration of magmatic minerals; (3) oxidized fluid stage (magnetite–epidote group minerals mineralization); and (4) reduced fluid stage (pyrite mineralization). 相似文献
2.
E. H. Brown 《Contributions to Mineralogy and Petrology》1977,64(2):123-136
Phase relations of pumpellyite, epidote, lawsonite, CaCO3, paragonite, actinolite, crossite and iron oxide are analysed on an Al-Ca-Fe3+ diagram in which all minerals are projected from quartz, albite or Jadeite, chlorite and fluid. Fe2+ and Mg are treated as a single component because variation in Fe2+/Mg has little effect on the stability of phases on the diagram. Comparison of assemblages in the Franciscan, Shuksan, Sanbagawa, New Caledonia, Southern Italian, and Otago metamorphic terranes reveals several reactions, useful for construction of a petrogenetic grid:
- lawsonite+crossite + paragonite = epidote+chlorite + albite + quartz + H2O
- lawsonite + crossite = pumpellyite + epidote + chlorite + albite+ quartz + H2O
- crossite + pumpellyite + quartz = epidote + actinolite + albite + chlorite + H2O
- crossite + epidote + quartz = actinolite + hematite + albite + chlorite + H2O
- calcite + epidote + chlorite + quartz = pumpellyite + actinolite + H2O + CO2
- pumpellyite + chlorite + quartz = epidote + actinolite + H2O
3.
Kentaro Nakamura 《Geochimica et cosmochimica acta》2004,68(22):4595-4618
Early Archean (3.46 Ga) hydrothermally altered basaltic rocks exposed near Marble Bar, eastern Pilbara Craton, have been studied in order to reveal geological and geochemical natures of seafloor hydrothermal carbonatization and to estimate the CO2 flux sunk into the altered oceanic crust by the carbonatization. The basaltic rocks are divided into basalt and dolerite, and the basalt is further subdivided into type I, having original igneous rock textures, and type II, lacking these textures due to strong hydrothermal alteration. Primary clinopyroxene phenocrysts are preserved in some part of the dolerite samples, and the alteration mineral assemblage of dolerite (chlorite + epidote + albite + quartz ± actinolite) indicates that the alteration condition was typical greenschist facies. In other samples, all primary minerals were completely replaced by secondary minerals, and the alteration mineral assemblage of the type I and type II basalts (chlorite + K-mica + quartz + carbonate minerals ± albite) is characterized by the presence of K-mica and carbonate minerals and the absence of Ca-Al silicate minerals such as epidote and actinolite, suggesting the alteration condition of high CO2 fugacity. The difference of the alteration mineral assemblages between basalt and dolerite is probably attributed to the difference of water/rock ratio that, in turn, depends on their porosity.Carbonate minerals in the carbonatized basalt include calcite, ankerite, and siderite, but calcite is quite dominant. The δ13C values of the carbonate minerals are −0.3 ± 1.2‰ and mostly within the range of marine carbonate, indicating that the carbonate minerals were formed by seafloor hydrothermal alteration and that carbonate carbon in the altered basalt was derived from seawater. Whole-rock chemical composition of the basaltic rocks is essentially similar to that of modern mid-ocean ridge basalt (MORB) except for highly mobile elements such as K2O, Rb, Sr, and Ba. Compared to the least altered dolerite, all altered basalt samples are enriched in K2O, Rb, and Ba, and are depleted in Na2O, reflecting the presence of K-mica replacing primary plagioclase. In addition, noticeable CO2 enrichment is recognized in the basalt due to the ubiquitous presence of carbonate minerals, but there was essentially neither gain nor loss of CaO. This suggests that the CO2 in the hydrothermal fluid (seawater) was trapped by using Ca originally contained in the basalt. The CaO/CO2 ratios of the basalt are generally the same as that of pure calcite, indicating that Ca in the basalt was almost completely converted to calcite during the carbonatization, although Mg and Fe were mainly redistributed into noncarbonate minerals such as chlorite.The carbon flux into the Early Archean oceanic crust by the seafloor hydrothermal carbonatization is estimated to be 3.8 × 1013 mol/yr, based on the average carbon content of altered oceanic crust of 1.4 × 10-3 mol/g, the alteration depth of 500 m, and the spreading rate of 1.8 × 1011 cm2/yr. This flux is equivalent to or greater than the present-day total carbon flux. It is most likely that the seafloor hydrothermal carbonatization played an important role as a sink of atmospheric and oceanic CO2 in the Early Archean. 相似文献
4.
5.
Rosia Poieni copper deposit,Apuseni Mountains,Romania: advanced argillic overprint of a porphyry system 总被引：2，自引：0，他引：2
The Rosia Poieni deposit is the largest porphyry copper deposit in the Apuseni Mountains, Romania. Hydrothermal alteration and mineralization are related to the Middle Miocene emplacement of a subvolcanic body, the Fundoaia microdiorite. Zonation of the alteration associated with the porphyry copper deposit is recognized from the deep and central part of the porphyritic intrusion towards shallower and outer portions. Four alteration types have been distinguished: potassic, phyllic, advanced argillic, and propylitic. Potassic alteration affects mainly the Fundoaia subvolcanic body. The andesitic host rocks are altered only in the immediate contact zone with the Fundoaia intrusion. Mg-biotite and K-feldspar are the main alteration minerals of the potassic assemblage, accompanied by ubiquitous quartz; chlorite, and anhydrite are also present. Magnetite, pyrite, chalcopyrite and minor bornite, are associated with this alteration. Phyllic alteration has overprinted the margin of the potassic zone, and formed peripheral to it. It is characterized by the replacement of almost all early minerals by abundant quartz, phengite, illite, variable amounts of illite-smectite mixed-layer minerals, minor smectite, and kaolinite. Pyrite is abundant and represents the main sulfide in this alteration zone. Advanced argillic alteration affects the upper part of the volcanic structure. The mineral assemblage comprises alunite, kaolinite, dickite, pyrophyllite, diaspore, aluminium-phosphate-sulphate minerals (woodhouseite-svanbergite series), zunyite, minamyite, pyrite, and enargite (luzonite). Alunite forms well-developed crystals. Veins with enargite (luzonite) and pyrite in a gangue of quartz, pyrophyllite and diaspore, are present within and around the subvolcanic intrusion. This alteration type is partially controlled by fractures. A zonal distribution of alteration minerals is observed from the centre of fractures outwards with: (1) vuggy quartz; (2) quartz + alunite; (3) quartz + kaolinite ± alunite and, in the deeper part of the argillic zone, quartz + pyrophyllite + diaspore; (4) illite + illite-smectite mixed-layer minerals ± kaolinite ± alunite, and e) chlorite + albite + epidote. Propylitic alteration is present distal to all other alteration types and consists of chlorite, epidote, albite, and carbonates. Mineral parageneses, mineral stability fields, and alteration mineral geothermometers indicate that the different alteration assemblages are the result of changes in both fluid composition and temperature of the system. The alteration minerals reflect cooling of the hydrothermal system from >400 °C (biotite), to 300–200 °C (chlorite and illite in veinlets) and to lower temperatures of kaolinite, illite-smectite mixed layers, and smectite crystallization. Hydrothermal alteration started with an extensive potassic zone in the central part of the system that passed laterally to the propylitic zone. It was followed by phyllic overprint of the early-altered rocks. Nearly barren advanced argillic alteration subsequently superimposed the upper levels of the porphyry copper alteration zones. The close spatial association between porphyry mineralization and advanced argillic alteration suggests that they are genetically part of the same magmatic-hydrothermal system that includes a porphyry intrusion at depth and an epithermal environment of the advanced argillic type near the surface.Editorial handling: B. Lehmann 相似文献
6.
Spencer J. Cotkin 《Contributions to Mineralogy and Petrology》1987,96(2):192-200
The Late Ordovician schist of Skookum Gulch, northern California, is one of only a few pre-Mesozoic blueschist localities in North America. Among these, the Skookum Gulch occurrence is noteworthy because it contains lawsonite and has had a relatively simple metamorphic and structural history.Numerous assemblages and a wide variation in the modal proportion of minerals are present due to a spectrum of bulk compositions. This is reflected in the composition of Na-amphibole, which varies from ferro-glaucophane, glaucophane, and crossite (±magnetite) to magnesio-riebeckite (+hematite). Application of the available experiments and empirically calibrated equilibria to the assemblages glaucophane+lawsonite+chlorite+quartz+albite and glaucophane+actinolite+epidote+chlorite+quartz+albite yield estimates of temperature and pressure near T= 275° C and P=7.0 kbar. Estimates of uncertainty are difficult to assess, but are no more than ±100° C and ±3.0 kbar, and are probably considerably smaller. Calcite +quartz+sphene and calcite+quartz+actinolite indicate an extremely H2O-rich fluid (X(CO2)<0.003).The absence of a greenschist facies overprint indicates that the schist of Skookum Gulch was uplifted soon after metamorphism. However, it was not exposed until the recent geologic past, having resided at shallow crustal levels for approximately 400 Ma. 相似文献
7.
Characteristic Features of REE and Pb–Zn–Ag Mineralizations in the Na Son Deposit,Northeastern Vietnam 下载免费PDF全文
下载免费PDF全文 Can Pham‐Ngoc Daizo Ishiyama Tuan Anh Tran Mihoko Hoshino Sachihiro Taguchi 《Resource Geology》2016,66(4):404-418
The Na Son deposit is a small‐scale Pb–ZnPb–Zn–Ag deposit in northeast Vietnam and consists of biotite–chlorite schist, reddish altered rocks, quartz veins and syenite. The biotite–chlorite schist is intruded by syenite. Reddish altered rocks occur as an alteration halo between the biotite–allanite‐bearing quartz veins and the biotite–chlorite schist. Allanite occurs in the biotite–allanite‐bearing quartz veins and in the proximal reddish altered rocks. Rare earth element (REE) fluorocarbonate minerals occur along fractures or at rim of allanite crystals. The later horizontal aggregates of sulfide veins and veinlets cut the earlier reddish altered rocks. The earlier Pb–Zn veins consist of a large amount of galena and lesser amounts of sphalerite, pyrite and molybdenite. The later Cu veins cutting the Pb–Zn veins include chalcopyrite and lesser amounts of tetrahedrite and pyrite. The occurrences of two‐phase H2O–CO2 fluid inclusions in quartz from biotite–allanite‐bearing quartz veins and REE‐bearing fluorocarbonate minerals in allanite suggest the presence of CO2 and F in the hydrothermal fluid. The oxygen isotopic ratios of the reddish altered rocks, biotite–chlorite schist, and syenite range from +13.9 to +14.9 ‰, +11.5 to +13.3 ‰, and +10.1 to +11.6 ‰, respectively. Assuming an isotopic equilibrium between quartz (+14.6 to +15.8 ‰) and biotite (+8.6 ‰) in the biotite–allanite‐bearing quartz vein, formation temperature was estimated to be 400°C. At 400°C, δ18O values of the hydrothermal fluid in equilibrium with quartz and biotite range from +10.5 to +11.7 ‰. These δ18O values are consistent with fluid that is derived from metamorphism. Assuming an isotopic equilibrium between galena (+1.5 to +1.7 ‰) and chalcopyrite (+3.4 ‰), the formation temperature was estimated to be approximately 300°C. The formation temperature of the Na Son deposit decreased with the progress of mineralization. Based on the geological data, occurrence of REE‐bearing minerals and oxygen isotopic ratios, the REE mineralization is thought to result from interaction between biotite–chlorite schist and REE‐, CO2‐ and F‐bearing metamorphic fluid at 400°C under a rock‐dominant condition. 相似文献
8.
斑岩型矿床具有十分广泛和明显的热液蚀变带,青磐岩化通常位于中心钾化带外侧,可分为三个亚带,绿帘石是青磐岩化带最重要的蚀变矿物之一,但目前对青磐岩化带内各亚带之中的绿帘石的特征研究较为薄弱。近年来,短波红外光谱技术(SWIR)已经广泛应用于热液蚀变矿物的识别,但由于短波红外光谱通过识别特定的基团进而识别含此基团的矿物,难以识别斑岩中部分关键蚀变矿物,如钾长石、钠长石和硬石膏。X射线衍射技术(XRD)能识别大部分蚀变矿物,可对红外光谱技术在斑岩矿床中的应用进行补充。本文以江西省德兴地区富家坞矿区为研究对象,提出应用SWIR和XRD分析辅助蚀变填图。富家坞矿区发育了十分广泛的绿帘石化,根据其共生矿物组合及空间分布,划分了三种绿帘石类型。第Ⅰ类:矿物组合为绿帘石-钠长石-石英-方解石,绿帘石和钠长石以脉状形式产出于钾化花岗闪长斑岩体内,穿切钾长石斑晶;第Ⅱ类:矿物组合为绿帘石±绿泥石-石英-方解石,绿帘石和绿泥石以集合体形式交代早期岩体内黑云母、斜长石的方式产出,并保留有原生矿物晶型,伴有方解石、石英等矿物;第Ⅲ类绿帘石共生矿物主要为石英、方解石、沸石等,含少量高岭石,主要呈不规则脉状,分布于蚀变花岗闪长斑岩外侧。通过对以上三类绿帘石进行系统SWIR和XRD分析,发现类型Ⅰ绿帘石大部分表现出较大的Fe-OH吸收峰位值(Pos2252 2255),类型Ⅱ和类型Ⅲ绿帘石大部分表现为较小的Fe-OH吸收峰位值(Pos2252 2255)。XRD结果显示绿帘石晶体特征更为明显,特征衍射峰位值{■13}晶面表现出相对集中的特征,但是次峰{022}晶面表现出一定的差异性,且绿帘石{022}晶面2. 40?衍射峰半高宽(FWHM-2)与绿帘石Dep2334/Dep2252值呈现负相关的关系。故本文认为绿帘石的次峰{022}晶面2. 40?衍射峰值及其半高宽(FWHM-2)可以作为讨论斑岩矿床围岩蚀变矿物绿帘石的结晶度的主要参数。三种绿帘石结晶指数的差异可能是热液流体演化过程中温度降低和距离岩体中心的远近造成的。 相似文献
9.
A very coarse grained graywacke from Strassberg in the Lower Harz Mountains (Germany) consists of rock-fragments, feldspars, quartz, chlorites, micas, accessories and ores. Low grade metamorphic mineral reactions are indicated by the formation of 2M-muscovite +chlorite+sphene+albite in the matrix of the graywacke, by prehnite+chlorite+ sphene+calcite+sericite+albite (±quartz) in volcanic rock-fragments, and by prehnite +calcite+quartz along fine fissures. The newly formed minerals in the coarse grained graywacke belong to the laumontite-prehnite-quartz-facies of the burial metmorphism. However, the formation of the low grade minerals is caused by thermal metamorphism in outer contact zones of the Ramberg granite intrusion in the Strassberg area. 相似文献
10.
Occurrence of calcite in Sanbagawa pelitic schists: implications for the formation of garnet, rutile, oligoclase, biotite and hornblende 总被引：2，自引：0，他引：2
The frequency of occurrence of minerals in 1876 samples of Sanbagawa pelitic schist in central Shikoku is summarized on the basis of microscopic observation accompanied, in part, by use of an electron microprobe. All samples contain quartz, plagioclase, phengite, chlorite and graphite. More than 90% of samples contain clinozoisite, titanite and apatite. Garnet is present in 95% of samples from the garnet zone, and biotite is present in 64% of samples from the albite‐biotite zone. Calcite is found in about 40% of samples of the pelitic schist collected from outcrop, but occurs in 95% of the pelitic schist from drill cores. Calcite was apparently ubiquitous in the pelitic schist during the Sanbagawa metamorphism, but must have been dissolved recently by the action of surface or ground water. The mineral assemblages of the Sanbagawa pelitic schist have to be analyzed in the system with excess calcite, quartz, albite (or oligoclase), clinozoisite, graphite and fluid that is composed mainly of H2O, CO2 and CH4. In the presence of calcite, reactions that produce garnet, rutile, oligoclase, biotite and hornblende, some of which define isograds of the metamorphic belt, should be written as mixed volatile equilibria that tend to take place at lower temperature than the dehydration reactions that have been proposed. The presence of calcite in pelitic schist suggests that fluid composition is a variable as important in determining mineral assemblages as pressure and temperature. Thus Ca‐bearing phases must be taken into account to analyze the phase relations of calcite‐bearing pelitic schist, even if CaO content of Sanbagawa pelitic schist is low. As calcite is a common phase, the mineral assemblages of the biotite zone pelitic schist may contravene the mineralogical phase rule and warrant further study. 相似文献
11.
Despite a great interest in Brazilian Equatorial Margin exploration, very little was published on the diagenesis of sandstones from that area. A wide recognition petrographic study was performed to identify the major diagenetic processes that impacted the porosity of Lower Cretaceous sandstones of the Pará-Maranhão, São Luís, Bragança-Viseu and Barreirinhas basins. Arkoses from the Pará-Maranhão Basin show neoformed or infiltrated clay coatings, mica replacement and expansion by kaolinite and vermiculite, and precipitation of grain-replacive and pore-filling quartz, kaolinite, albite, chlorite, calcite, dolomite, siderite, pyrite and titanium oxides. Compaction, quartz and calcite cementation were the main porosity-reducing processes. Barreirinhas Basin lithic arkoses and subarkoses display clay coatings, compaction of metamorphic fragments into pseudomatrix, and precipitation of grain-replacive and pore-filling kaolinite, quartz, albite, chlorite, calcite, dolomite, TiO2 and pyrite. The main porosity-reducing processes were calcite cementation in the subarkoses, and compaction and quartz cementation in lithic arkoses. Quartzarenites from this basin were early- and pervasively cemented by dolomite. Arkoses and lithic arkoses of the São Luís and Bragança-Viseu basins show clay coatings, pseudomatrix from mud intraclasts compaction, and precipitation of pore-filling and grain-replacive kaolinite, vermiculite, smectite, quartz, albite, chlorite, illite, calcite, dolomite, hematite, TiO2 and pyrite. Compaction of mud intraclasts and dissolution of feldspars and heavy minerals were the main porosity-modification processes. These preliminary results may contribute to the understanding of the spatial and temporal distribution of the diagenetic processes and their impacts on the porosity of the sandstones from these basins. 相似文献
12.
Mineral paragenescs in the prehnite-pumpellyite to greenschistfades transition of the Karmutsen metabasites are markedly differentbetween amygdule and matrix, indicating that the size of equilibriumdomain is very small. Characteristic amygdule assemblages (+chlorite + quartz) vary from: (1) prehnite + pumpeUyite + epidote,prehnite + pumpellyite + calcite, and pumpellyite + epidote+ calcite for the prehnite-pumpellyite facies; through (2) calcite+ epidote + prehnite or pumpellyite for the transition zone;to (3) actinolite + epidote + calrite for the greenschist facies.Actinolite first appears in the matrix of the transition zone.Na-rich wairakites containing rare analcime inclusions coexistwith epidote or Al-rich pumpellyite in one prehnite-pumpellyitefacies sample. Phase relations and compositions of these wairakite-bearingassemblages further suggest that pumpellyite may have a compositionalgap between 0.10 and 0.15 XFe?. Although the facies boundaries are gradational due to the multi-varianceof the assemblages, several transition equilibria are establishedin the amygdule assemblages. At low Xco2, pumpellyite disappearsprior to prehnite by a discontinuous-type reaction, pumpellyite+ quartz + CO2 = prehnite + epidote + calcite + chlorite + H2O,whereas prehnite disappears by a continuous-type reaction, prehnite+ CO2 = calcite + epidote + quartz-l-H2O. On the other hand,at higher XCO2 a prehnite-out reaction, prehnite + chlorite+ H2O + CO2 = calcite + pumpellyite + quartz, precedes a pumpellyiteoutreaction, pumpellyite + CO2 = calcite + epidote + chlorite +quartz + H2O. The first appearance of the greenschist faciesassemblages is defined at both low and high XCOj by a reaction,calcite + chlorite + quartz = epidote + actinolite+ H2O + CO2.Thus, these transition equilibria are highly dependent on bothXFe3+ + of Ca-Al silicates and XH20 of the fluid phase. Phaseequilibria together with the compositional data of Ca-Al silicatesindicate that the prehnite-pumpellyite to greenschist faciestransition for the Karmutsen metabasites occurred at approximately1.7 kb and 300?C, and at very low Xco2, probably far less than0.1. 相似文献
13.
Calcic schists in the andalusite-type regional metamorphic terrainin the Panamint Mountains, California, contain the low-varianceassemblage quartz+epidote+muscovite+biotite+calcic amphibole+chlorite+plagioclase+spheneat low grade. Near the sillimanite isograd, chlorite in thisassemblage is replaced by garnet. The low variance in many calcicschists allows the determination of the nature of the reactionthat resulted in the coexistence of garnet+hornblende. A graphicalanalysis of the mineral assemblages shows that the reactioncan not be of the form biotite+epidote+chlorite+plagioclase+quartz=garnet+hornblende+muscovite+sphene+H2Obecause garnet+chlorite never coexisted during metamorphismand the chlorite-bearing and garnet-bearing phase volumes donot overlap. The compositions of the minerals show that withincreasing grade amphibole changed from actinolite to pargasitichornblende with no apparent miscibility gap, the partitioningof Fe and Mg between chlorite and hornblende changed from KD(Mg/Fe, chl&) < 1 to KD > 1, the partitioning betweenbiotite and hornblende changed from KD (Mg/Fe, bio/amp) <1 in chlorite-zone samples to KD > 1 in garnet + hornblende-zonesamples, and the transition to the garnet-bearing assemblageoccurred when the composition of plagioclase was between An55and An80. Both the graphical analysis and an analytical analysisof the compositions of the minerals using simplified componentsderived from the natural mineral compositions indicate thatat the garnet+hornblende isograd the composition of hornblendewas colinear with that of plagioclase and biotite, as projectedfrom quartz, epidote, muscovite, and H2O. During progressivemetamorphism, chlorite+biotite+epidote+quartz continuously brokedown to form hornblende+muscovite+sphene until the degeneracywas reached. At that point, tie lines from hornblende couldextend to garnet without allowing garnet to coexist with chlorite.Thus, the garnet+hornblende isograd was established throughcontinuous reactions within the chlorite-grade assemblage ratherthan through a discontinuous reaction. In this type of isograd,the low-grade diagnostic assemblage occurs only in Mg-rich rocks;whereas the high-grade assemblage occurs only in Fe-rich rocks.This relation accounts for the restricted occurrence of garnet+hornblendeassemblage in low-pressure terrains. In Barrovian terrains,garnet+chlorite commonly occurs, and the first appearana ofgarnet+hornblende can simply result from the continuous shiftof the garnet+chlorite tie line to Mg-rich compositions. 相似文献
14.
Drilling through the Palaeoproterozoic bedrock at Forsmark, central Sweden, during the site investigation for a potential geological repository of highly radioactive nuclear waste has provided high quality drill-core material from the upper 1 km of the Fennoscandian Shield. Analyses of stable isotopes (δ13C, δ18O, δ34S, 87Sr/86Sr), rare earth elements and fluid inclusions in fracture filling calcite and pyrite from these drill cores have resulted in the discrimination of several episodes of fracture mineralisations. These events represent migration of fluids during a wide range of conditions, ranging from high-temperature hydrothermal to present-day groundwater circulation. Four major events have been distinguished: 1) Precipitation of epidote, chlorite and quartz under hydrothermal conditions (T > 150–200 °C) during the Proterozoic, sometime between 1.8 and 1.1 Ga. 2) Hydrothermal circulation at temperatures close to 200 °C with precipitation of adularia, albite, prehnite, laumontite, calcite and chlorite. Most of these minerals precipitated during a tectonothermal event between 1.1 and 1.0 Ga, possibly in response to far-field effects of the Sveconorwegian orogeny. 3) Precipitation of mainly quartz, calcite, pyrite and asphaltite occurred during the Palaeozoic, at temperatures between 60 and 190 °C (mainly at < 100 °C). Mixing of a fluid emanating from an organic rich overlying sedimentary cover and a deep basinal fluid from the crystalline bedrock is suggested to have caused this precipitation, possibly as a far-field response to the Caledonian orogeny and/or the development of the Caledonian foreland basin. 4) The youngest generation of fracture minerals is associated with formation of clay minerals and calcite with minor occurrences of pyrite and goethite. These minerals have probably precipitated episodically during a long time period (possibly from the Late Palaeozoic to the present) from various fluids at low temperature conditions (< 50 °C). Few calcites in equilibrium with the present groundwater suggest that the ongoing precipitation of calcite is very limited. 相似文献
15.
陕西省铧厂沟金矿床位于勉略缝合带以南,矿体受控于近东西向逆冲断层和韧脆性剪切带。本文以细碧岩矿带为例,系统研究了围岩蚀变分带及蚀变矿物组合,总结了矿床的蚀变分带模式。围岩蚀变以穿切细碧岩透镜体的剪切带为中心向外依次可划分为黄铁绢英岩化带、绢云碳酸盐化带和绿泥赤铁矿化带。蚀变矿物组合分别为黄铁矿＋铁白云石＋铬云母＋绢云母＋钠长石＋石英＋方解石、铁白云石＋绢云母＋钠长石＋石英±黄铁矿、（铁）绿泥石＋钠长石＋铁白云石＋赤铁矿＋钛铁氧化物＋石英±绿帘石。蚀变岩石组分迁移分析表明,在围岩蚀变过程中, SiO2、Na2O、Fe2O3T、MgO与Y等组分发生不同程度的迁出, K2O、CaO、Ba、Rb、Sr、Cr、Cu、Pb和挥发组分等迁入,并以黄铁绢英岩化带最为显著。金在成矿流体中以Au（HS）–2络合物迁移,成矿流体与富铁细碧岩之间的反应是金沉淀重要机制。 相似文献
16.
Basalt in the Furutobe District of the Kuroko mine area in Japan is characterized by abundant chlorite and epidote. Fluid inclusion studies indicate that chlorite is formed at lower temperatures (230–250°C) than epidote (250–280°C). The seawater/basalt mass ratio for the early chlorite-rich alteration was high (max. 40), but that for the later alteration was low (0.1–1.8). The CaO, Na2O and SiO2 of the bulk rock correlate negatively with MgO, while FeO and Σ Fe correlate positively with MgO. These changes in the characteristic features of hydrothermal alteration from early to late are generally similar to those for a mid-ocean ridge geothermal system accompanying basalt alteration.The MgO/FeO ratios of chlorite and actinolite and the Fe2O3 concentration of epidote from the basalt are greater than those of mid-ocean ridge basalt probably owing to the differences in the Fe2O3/FeO and MgO/FeO ratios of the parent rocks. The lower CaO concentration and the higher Na2O concentration of the bulk rock compared with altered mid-ocean ridge basalt can be interpreted in terms of the difference in original bulk rock compositions.The Furutobe basalt, as well as other submarine back arc basalts, contains more vesicles filled with hydrothermal minerals (epidote, calcite, quartz, chlorite, pyrite) than do the mid-ocean ridge basalts. The abundance of vesicles plays an important role in controlling the secondary mineralogy and geochemistry of hydrothermally altered submarine back arc basin basalts. 相似文献
17.
In the Raposos orogenic gold deposit, hosted by banded iron-formation (BIF) of the Archean Rio das Velhas greenstone belt, the hanging wall rocks to BIF are hydrothermally-altered ultramafic schists, whereas metamafic rocks and their hydrothermal schistose products represent the footwall. Planar and linear structures at the Raposos deposit define three ductile to brittle deformational events (D1, D2 and D3). A fourth group of structures involve spaced cleavages that are considered to be a brittle phase of D3. The orebodies constitute sulfide-bearing D1-related shear zones of BIF in association with quartz veins, and result from the sulfidation of magnetite and/or siderite. Pyrrhotite is the main sulfide mineral, followed by lesser arsenopyrite and pyrite. At level 28, the hydrothermal alteration of the mafic and ultramafic wall rocks enveloping BIF define a gross zonal pattern surrounding the ore zones. Metabasalt comprises albite, epidote, actinolite and lesser Mg/Fe–chlorite, calcite and quartz. The incipient stage includes the chlorite and chlorite-muscovite alteration zone. The least-altered ultramafic schist contains Cr-bearing Mg-chlorite, actinolite and talc, with subordinate calcite. The incipient alteration stage is subdivided into the talc–chlorite and chlorite–carbonate zone. For both mafic and ultramafic wall rocks, the carbonate–albite and carbonate–muscovite zones represent the advanced alteration stage.Rare earth and trace element analyses of metabasalt and its alteration products suggest a tholeiitic protolith for this wall rock. In the case of the ultramafic schists, the precursor may have been peridotitic komatiite. The Eu anomaly of the Raposos BIF suggests that it was formed proximal to an exhalative hydrothermal source on the ocean floor. The ore fluid composition is inferred by hydrothermal alteration reactions, indicating it to having been H2O-rich containing CO2 + Na+ and S. Since the distal alteration halos are dominated by hydrated silicate phases (mainly chlorite), with minor carbonates, fixation of H2O is indicated. The CO2 is consumed to form carbonates in the intermediate alteration stage, in halos around the chlorite-dominated zones. These characteristics suggest variations in the H2O to CO2-ratio of the sulfur-bearing, aqueous-carbonic ore fluid, which interacted at varying fluid to rock ratios with progression of the hydrothermal alteration. 相似文献
18.
B. Ronald Frost 《Contributions to Mineralogy and Petrology》1980,73(4):365-373
Using graphical analysis of the system CaO-Al2O3-SiO2-H2O-CO2, this paper derives a topology relating the minerals calcite, laumontite, wairakite, prehnite, quartz, and zoisite. Simple thermodynamic reasoning allows this system to be applied to natural rocks and indicates that the first appearance of the assemblage epidote-chlorite-quartz (±albite) should mark the upper boundary of zeolite facies. This assemblage forms at the expense of laumontite+prehnite, laumontite+calcite, or laumontite+pumpellyite, with wairakite likely to replace laumontite as the stable zeolite at low pressures. In natural systems this proposed facies boundary is multivariant and, hence, it is likely to be strongly sensitive to compositional variables. For example, Na-bearing wairakite will be more stable than pure Ca-wairakite and increasing abundance of Fe3+ will tend to stabilize epidote+quartz at the expense of the zeolites. Because of this, monitoring the composition of minerals such as epidote, prehnite, or wairakite from lowvariance assemblages may provide a more-sensitive indicator of metamorphic grade than the presence or absence of any particular mineral assemblage. 相似文献
19.
Tadao Nishiyama 《Contributions to Mineralogy and Petrology》1990,104(1):35-46
Local fluid migration through a serpentine melange caused successive carbonation of a metabasite block (about 80 meter in diameter) during the uplift stage of the glaucophanitic metamorphic rocks, the Nishisonogi metamorphics, southwest Japan. The block shows a zonal sequence as follows. Zone 1: original greenschist (Am+Ep+ Chl+Ab+Sph+Qtz). Zone 2: epidote disappears by the reaction Ep+Am+CO2+H2O=Chl+Cc+Qtz. Zone 3: balc appears by the reaction Am+CO2+H2O=Ta+Cc+ Qtz. Zone 4:sphene breakdowns by the reaction Sph+ CO2=Rt+Cc+Qtz. Zone 5: amphibole disappears by the two simultaneous reactions, Am+CO2=Do+Ta+Qtz and Ta+Cc+CO2=Do+Qtz+H2O. Zone 7: albite is replaced by chlorite, calcite, dolomite and quartz, and the assemblage of Do+Cc+Chl+Rt+Qtz is stable. Analyses of phase relations indicate an introduction of CO2-rich fluid into the greenschist body during regional metamorphism. The CO2-rich fluid may have formed by devolatilization reactions between serpentinite and graphite-bearing metasediments. The fluid migrated within the melange through a channelized pathway and into the greenschist body from a deeper part of the melange. 相似文献
20.
Thermodynamic numerical simulations were carried out to determine the principal simple and complex migration species of Ca, Mg, Na, K, Al, B, Mn, Mo, Sr, and U with Cl–, OH–, SO4?2, HCO3?, and CO32? in waters at the Lomonosov diamond deposit and to estimate the saturation indexes with respect to kaolinite, Na- and Mg-montmorillonite, Mg- and Na-saponite, muscovite and paragonite, biotite, phlogopite, chromite, pyrite, plagioclase (anorthite, labradorite, and andesine), olivine (forsterite and fayalite), diopside, pyrope, gypsum, anhydrite, barite, magnesite, calcite, dolomite, talc, chrysotile, chlorite, goethite, quartz, microcline, and albite. The waters are proved not to be saturated with respect to the primary (hydrothermal) minerals. The saturation of certain water samples with uranophane suggests that this mineral is of secondary genesis. The ascent of highly mineralized deep waters shall result in the dissolution of minerals whose concentrations are near the saturation ones. To maintain the ecological standards of the discharged waters, they should be diluted and/or purified by adsorbing dissolved U on a reducing reactive barrier. 相似文献