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1.
Variations in chemistry and related physical properties of sheet silicates in the Ouégoa district with metamorphic grade are investigated. Weakly metamorphosed rocks prior to the crystallization of lawsonite contain phengite (d 006=3.317–3.323 Å), chlorite and occasionally paragonite while interstratified basaltic sills contain chlorite, minor phengite and stilpnomelane. Pyrophyllite crystallizes before lawsonite in some metamorphosed acid tuffs and is also stable in the lawsonite zone. Paragonite, phengite and chlorite appear to be stable through the sequence from weakly metamorphosed rocks into high-grade “eclogitic” schists and gneisses. Optical, chemical and some X-ray diffraction data is given for representative sheet silicates. Electron probe analyses of 55 phengites, 21 paragonites, 57 chlorites, 12 vermiculites, 2 stilpnomelanes, and 2 chloritoids are presented in graphical form. All K-micas analysed are consistently phengitic (3.29–3.55 Siiv ions per formula unit) and show limited solid solution with paragonite (4 to 13% Pa). The K∶Na ratio of the phengite is strongly dependant on the assemblage in which it occurs; the amount of phengite component and its Fe∶Mg ratio depends on bulk-rock composition. Phengites from acid volcanics have the highest Fe∶Mg ratio, highest phengite component and β refractive indices. Phengites from basic volcanics and metasediments of the epidote zone have the lowest Fe∶Mg ratio. Phengites from lawsonite-zone metasediments have intermediate Fe∶Mg ratios. The phengites show a small decrease in phengite component with increasing metamorphic grade. d 006 for phengites varied from 3.302 to 3.323 Å but at least in the lawsonite and epidote zones appears to reflect composition and had little systematic variation with metamorphic grade; phengites from very low-grade rocks showed the longest values of d 006. Paragonite shows almost no phengite-type substitution and only limited solid solution (4–12%) with muscovite. All paragonites (6) and most phengites (20) which have been examined are 2M1 polymorphs; one Fe2+-phengite appears to be a 1M polymorph. The chemistry of chlorites closely reflects parent-rock chemistry. Chlorites from metasediments have distinctly higher Fe/(Fe+Mg) ratios than chlorites from basic igneous rocks; chlorites from the lawsonite and lawsonite-epidote transitional zone metasediments have the highest Fe/(Fe+Mg) ratios. In metabasalts Fe/(Fe+Mg) ratios appear to reflect individual variations in bulk-rock chemistry and show no direct correlation with metamorphic grade. There is little difference in Al/(Si+Al) ratio between chlorites from sediments and basic igneous rocks although in both lithologies the chlorites from the epidote zone appear to be slightly more aluminous. Fe-rich chlorites of the lawsonite zone metasediments have been altered by a process involving leaching of Fe and Mg and introduction of alkalies to a brown pleochroic Fe-vermiculite. Chemical and physical data for this vermiculite are given. The decrease in Fe/(Fe+Mg) ratio in chlorites and phengites on passing from the lawsonite to the epidote zone can be correlated with the crystallization of Fe-rich epidote and almandine in the epidote zone. Elemental partitioning between coexisting minerals has shown Ti to be partitioned into phengite, while Fe and Mn are strongly partitioned into chlorite. When either stilpnomelane or chloritoid coexists with phengite or chlorite, Fe and Mn are slightly enriched in the stilpnomelane or chloritoid relative to the chlorite.  相似文献   

2.
Moderately manganiferous siliceous pelagites near Meyers Pass, Torlesse Terrane, South Canterbury, New Zealand, have been metamorphosed in the prehnite–pumpellyite facies. A conodont colour index measurement suggests T max in the range 190–300 °C. Porphyroblastic manganaxinite, manganoan pumpellyite, manganoan chlorite and trace spessartine-rich garnet and sphalerite have formed in an extremely fine-grained quartz–albite–berthierine–phengite–titanite groundmass. Porphyroblastic manganaxinite semischists and schists are distinctive rocks in prehnite–pumpellyite to lower-grade greenschist and blueschist facies of New Zealand and Japan. Mn in the manganoan pumpellyites substitutes for Ca in W sites. Total Fe/(Fe+Mg) ratios in chlorite are dependent on oxidation state, being ≤0.22 in red hematitic hemipelagites, and ≥0.61 in low-f O2 grey metapelagites. In the low-f O2 metapelagites, manganoan berthierine with little or no chlorite is inferred in the groundmass and iron-rich chlorite occurs as porphyroblasts and veinlets, whereas in the red rocks, Mg-rich chlorite occurs both in groundmasses and veinlets. Variably high Si in the manganoan chlorites correlates with evidence for contaminant phases. The Mn content of chlorite contributing to garnet growth is dependent on metamorphic grade; incipient spessartine indicates a saturation value of 6–8% MnO in chlorite in low-f O2 rocks at Meyers Pass. Lower MnO contents are recorded for otherwise analogous rocks with increasing metamorphic grade, but at a given grade coexisting chlorite and garnet are richer in Mn where f O2 is high. Manganaxinite and manganoan pumpellyite also contributed to reactions forming grossular–spessartine solid solutions. Formation of garnet in siliceous pelagites is dependent on both Mn and Ca content. The spessartine component increases with grade into the greenschist facies. Partial recrystallization of berthierine to chlorite and the growth of porphyroblastic patches of other minerals was facilitated by brittle fracture and access of fluids to an otherwise impermeable matrix; to this extent the very low-grade metamorphism was episodic.  相似文献   

3.
The Igarapé Bahia gold deposit has developed from weathering of a near-vertical hydrothermal Cu (Au) mineralization zone. The unweathered bedrock composed of chlorite schists is mainly metamorphosed basalts, pyroclastic and clastic sedimentary rocks and iron formation. Contents and Fe/(Fe + Mg) ratios of chlorites increase from distal country rock towards the mineralization zone, which can be attributed to different water/rock ratios and locations in a hydrothermal system. In the hydrothermal system high salinity fluids convected through basin-floor rocks, stripping metals from the recharge zones with precipitation in discharge zones. The chlorite with lower Fe/(Fe + Mg) ratios indicates alteration by relatively unreacted Mg-rich fluids, occurring within recharge zones. By contrast, the chlorite with higher Fe/(Fe + Mg) ratios in the mineralization zone formed from solutions rich in Fe, Mn, Au, Cu, H2S and SiO2 within a discharge zone. The iron formation could also be formed within the discharge zone or on the basin floor from the Fe-rich fluids. The distal country rock with less chlorite content is a hydrothermal product at low water/rock ratios whereas the proximal country rock and the host rock with more chlorite content formed at high water/rock ratio conditions. The Al(IV) contents of chlorites indicate that the formation temperatures of these rocks range from 204 to 266 °C, with temperatures slightly increasing from distal country rock towards the mineralization zone.  相似文献   

4.
In this study, we applied chemical geothermometers to the estimation of formation temperatures of chlorites from various types of hydrothermally altered rocks in the Toyoha geothermal field, using core samples from six drill holes (TH-2 to TH-7) together with wasted ore samples from Toyoha vein-type ore deposit. Based on the preliminary examination of mineral assemblages by X-ray powder diffraction and optical microscopy, hydrothermal alteration observed through the drill holes was classified into four types of alteration zones: propylitic, mixed-layer minerals, kaolin minerals, and ore mineralized zones. The mineral assemblage of the ore mineralized zone observed through TH-2, TH-4, and TH-6 is similar to those of Toyoha ore veins reported previously. The Fe3+/ΣFe ratios of chlorites were determined by X-ray photoelectron spectroscopy (XPS), in addition to the usual microprobe analyses. The ratios ranged from 0.20–0.26 for chlorites from the propylitic alteration zone and from 0.13 to 0.17 for those from the ore mineralized zone associated with sulfide minerals. After correcting the Fe3+ contents in the octahedral sites of chlorite structures, we obtained acceptable temperatures of the chlorite formation by application of geothermometers, for instance, a similar range of 150–300°C for chlorites from either the propylitic zone or the ore mineralized zone developed through TH-2, TH-4, and TH-6. Chlorites from the ore mineralized zone proximal to the Toyoha deposit are characterized by high Fe and Mn contents compared to the propylitic chlorites, which is similar to the Toyoha vein-filling chlorites; the formation temperatures were close to both the homogenization temperatures of fluid inclusions and the present subsurface temperatures measured through drill holes. Chlorites from the Toyoha ore veins, however, gave slightly higher formation temperatures (180–350°C) than those of chlorites from the ore mineralized zone in the drill cores. This suggests that several types of hydrothermal alteration occurred at different stages in the Toyoha geothermal field and the composition of product chlorite was controlled not only by the temperature but also the composition of fluid related to the formation. Reliable estimation of temperature for the chlorite formation provides basic information on evaluating correctly other physicochemical conditions prevalent at the formation.  相似文献   

5.
Microprobe analyses are performed on micas (biotite, muscovite and phlogopite) and chlorite from 1.9–1.8 Ga acid K- or Na-rich metavolcanics, cordierit-emica schists and manganiferous rocks from the Hästefält area in central Sweden. The results indicate that Fe-rich biotites and muscovites containing 10 to 25% celadonite and/or pyrophyllite are common in the K- and Na-rich metavolcanics. In the cordierite-mica schists the biotites are Mg-rich and the muscovites contain less than 10% celadonite and/or pyrophyllite. The predominant mica in the manganiferous rocks are phlogopite and less frequent rather pure muscovite. The chlorites show a wide range in composition, but principally those occurring in the K- and Na-rich metavolcanics are brunsvigite and diabantite and those in the cordierite-mica schists and the manganiferous rocks are mainly sheridanite and clinochlore. The chlorites of the manganiferous rocks show enrichment in Mn compared to those in other rock types. In general the compositional variations in the micas and less commonly chlorites are strongly controlled by rock type and fluid chemistry, particularly with respect to the ratio of FeO/(FeO+MgO). Estimates of maximum prograde metamorphic temperature, based on phyllosilicates and co-existing cordierite and garnets, indicate a value of up to 500° C.  相似文献   

6.
201、325和706铀矿床蚀变带绿泥石研究   总被引：3，自引：0，他引：3  
以岩矿鉴定结果和电子探针绿泥石分析数据为依据,将325、706花岗岩型铀矿床蚀变带绿泥石分为假象绿泥石和鳞片状绿泥石。后者由前者转变而成,转变过程中存在着铁的迁出与镁的加入,迁出的铁形成赤铁矿,可能是造成碱性蚀变带呈红色的原因之一。201、325铀矿床蚀变带绿泥石为铁镁绿泥石和蠕绿泥石,706铀矿床蚀变带绿泥石主要属密绿泥石和铁斜绿泥石,少数属铁镁绿泥石。研究发现绿泥石变种由蚀变带原岩的∑FeO与MgO比值大小决定,与铀矿蚀变带是否为酸性和碱性没有必然的对应关系;绿泥石晶胞中镁羟基和铝羟基相对比例大小不同,是导致其吸收位置在2259-2262nm和2348-2359nm的诊断性吸收峰发育程度存在差别的原因。  相似文献   

7.
The Southern Vanoise is localized in the internal part of the Western Alps, in the Briançonnais zone. In Vanoise the following units can be distinguished (Fig. 1): a pre-hercynian basement (micaschists, glaucophanites, basic rocks), a permian cover (micaschists) and a mesozoic-paleocene cover (carbonate rocks). This area has been affected by the alpine metamorphic event characterized here by high and intermediate pressure facies. The rocks paragenesis are often unbalanced.The paleozoic rocks (Table 1) contain mainly: quartz, albite, paragonite, phengite, blue amphibole, chlorite, green biotite, garnet (Table 2). These minerals were analysed by an electron microprobe (Tables 3, 4 and 5). Mineral composition is highly variable: glaucophane is zoned (Table 5), white micas are more or less substituted with phengite (3.22O3/FeO + MgO)<0.53] whereas the Al rich chlorites [(Al2O3/FeO + MgO)>0.6] are associated with the less substituted white micas (Si=3.2) (Tables 3 and 4). The phengites with a Si content 3.2 occur in rocks where the retromorphic evolution is the most pronounced and penetrative. A metamorphic evolution is characterized by the disappearance of glaucophane which corresponds to the appearance of Al rich chlorite and to the decrease of phengitic substitution.The samples analysis are plotted in the tetraedric diagram: K2O-Al2O3-Na2O, Al2O3-FeO, MgO, on which a special mathematical treatment was applied. This method calculates the location of rocks composition in the four minerals space. This location is internal when the per cent amounts of all four relevant minerals are positive, if any of them is negative, the point is external (Tables 6–9).In Southern Vanoise micaschists, 2 subfacies are successively present (Fig. 3):Subfacies I: glaucophane-chlorite-phengite (Si4+ 3.5)-paragonite. Then subfacies II: chlorite-albite-phengite (Si4+ 3.2)-paragonite.In basic rocks is found essentially: Subfacies III: glaucophane-garnet-phengite-paragonite or IV: glaucophane-garnet-phengite-albite. Then subfacies V: green biotite-chlorite-albite-paragonite.The assemblages I and II proceed through reaction: 2 glaucophane +1 paragonite+2 H2O4.2 albite + 1 chlorite.The assemblage V appears with reactions: 1.8 glaucophane +2 phengite0.4 chlorite+2 green biotite + 3.6 albite +0.4 H2O or 2 glaucophane +2 phengite +0.5 garnet+ 6 H2O2 green biotite +1 chlorite+4 albiteThese reactions are controlled by hydratation: the composition variation of phengite and associated chlorite during the metamorphic evolution determines the stability of some minerals (particularly the glaucophane in Na2O poor rocks).In same rocks the results of mathematical treatment is not consistent with the data (Tables 2, 6–9). This discrepancy corresponds to a desequilibrium between chlorite and phengite.These results imply a continuous metamorphic evolution between two stages (Fig. 6): a first stage (1) at 8 kb, 350 ° C; a second stage (2) at 2 to 3 kb, 400–450 ° C.  相似文献   

8.
湘南白腊水锡矿床位于骑田岭燕山期黑云母花岗岩中。绿泥石化是这一含矿花岗岩中常见的热液蚀变现象,对采自
钻孔的岩石样品研究发现,花岗岩的绿泥石化程度变化较大。本文选择三组绿泥石化蚀变程度显著不同的花岗岩样品进行
研究,探讨了与锡成矿密切相关的含矿花岗岩的绿泥石化作用。研究表明,不同程度绿泥石化花岗岩中的绿泥石,在产出
形式与化学成分上均表现出一系列明显不同的特征。依据绿泥石产出形式、化学成分、绿泥石化花岗岩地球化学等特征认
为,绿泥石对花岗岩造岩矿物的交代顺序为：角闪石、黑云母→斜长石、钾长石→石英;绿泥石形态特征的变化一方面与
绿泥石成分有关,另一方面与被其交代的造岩矿物晶体结构有关;花岗岩绿泥石化越强烈,全岩的烧失量和Zn含量就越
高,原岩的Cl丢失到蚀变流体中去的量也越多。随着花岗岩绿泥石化程度的加强,其绿泥石的主要成分含量会呈现出规律
性的变化。绿泥石的Si含量在绿泥石化过程中逐渐减少;长石遭受破坏溶解后释放出的Al在厘米尺度范围内发生迁移与再
分配,引起绿泥石Al含量的升高;Fe从热液中带入,蚀变花岗岩中绿泥石矿物含量的多少与水-岩反应体系中Fe的多少有
关;形成绿泥石所需的Mg主要来源于花岗岩暗色矿物内Mg的释放与再分配;Mn则主要由外部流体带入。  相似文献   

9.
Abstract: Crystalline limestone of the Sako-nishi area in the Kamioka Zn-Pb mine, central Japan, is depleted in 18O and 13C toward the center of mineralization due to interaction with hydrothermal fluids with a dominant meteoric water component. The relationship between isotopic composition and mineral assemblage, texture, the chemical composition of the minerals, and the bulk chemical composition in the limestone was examined. A decrease in the δ18OSMOW value correlated with: (1) increase of fine-grained calcite which is enriched in Mn and exhibits a bright cathodoluminescence, (2) progressive hy-drothermal alteration of clinopyroxene in the original limestone into tremolite within the weakly-altered zone, and into chlorite and actinolite within the strongly-altered zone, (3) dominance of hydrothermal chlorite in altered limestone having δ18O values of less than 10%. This chlorite was enriched in Fe compared to mafic minerals in the unaltered limestone. The enrichment of Fe and Mn was more conspicuous in calcite and chlorite in skarn deposits. The occurrence and chemical composition of hydrothermal minerals in the limestone, skarn, and ore indicate that the 18O–depleted zones were formed in the later stage from fluids, which were responsible for mineralization and skarnization, and for Fe and Mn enrichment. The Al, Mn, and Fe contents, and the ratios of Mg/(Mg+Mn+Fe), Al/Mg, and Mn/Sr in the hydrochloric acid leachate of limestone varied with decreasing δ18O and δ13C values, reflecting increases in high-Mn calcite and high-Fe chlorite. These indexes were useful for the identification of hydrothermally altered limestone. Furthermore, the potential score weighted by each index was more effective and accurate means of detecting promising mineralization zones. An anomalous potential score due to the presence of hydrothermal minerals in the outcropping limestone occurred along the Atotsu–1GO fault. This structure indicates that the skarn deposits of the Sako-nishi area belong to Mozumi-type Zn–Pb skarn deposits, in which fissures and faults served as major passages for the hydrothermal fluid. High-Mn carbonate and high-Fe chlorite widely occur in base-metal vein deposits and Zn-Pb type skarn deposits. Leaching of altered rock with hydrochloric acid in addition to stable isotope composition and cathodoluminescence imaging is effective for geochemical exploration for hydrothermal deposits because it makes possible the detection of the elemental composition of hydrothermal minerals such as chlorite and carbonate and because of the rapidity and convenience of analysis.  相似文献   

10.
在西湖凹陷花港组储层整体低渗的背景下,优质储层的发育往往伴随绿泥石的富集。通过薄片观察、X衍射分析和扫描电镜及能谱分析等研究,认为研究区绿泥石呈黏土包膜、孔隙衬里和孔隙充填3种产出状态。黏土包膜为同沉积期铁镁物质絮凝吸附形成,成分复杂。孔隙衬里是绿泥石最主要的产出状态：Ⅰ类孔隙衬里绿泥石在早压实期前后由黏土包膜重结晶形成,单晶呈半自形片状,铁镁质量分数较低,排列杂乱;Ⅱ类孔隙衬里绿泥石在早压实期后由孔隙流体在洁净的颗粒表面结晶而成,单晶呈相对自形六方片状,铁镁质量分数较高,多垂直颗粒表面有序排列。孔隙充填绿泥石可细分为分散片状、书页状和绒球状,与溶蚀作用密切相关,单晶自形程度和铁镁质量分数均最高。黏土包膜绿泥石对储层物性的影响较小,但有助于衬里绿泥石的形成;孔隙衬里绿泥石难以缓解压实作用,但能够在一定程度上抑制压溶作用和有效地抑制早期石英加大,其中Ⅰ类孔隙衬里绿泥石由于连续性较好、排列杂乱、结晶较差和晶间孔复杂,对硅质胶结抑制作用明显,而Ⅱ类孔隙衬里绿泥石则相反,对硅质胶结的抑制作用有限;孔隙充填绿泥石仅充填较大原生粒间孔和粒间溶孔,对渗透率影响较小,仅在一定程度上减小了孔隙度。现今储层物性更多受控于储层砂岩的原始沉积组构以及相应的压实和溶蚀强度的改造过程,绿泥石的富集对优质储层具指示作用。  相似文献   

11.
Ninety-seven mineral phases consisting of ten chloritoids, fifteen epidotes, sixteen garnets, four sphenes, seven rutiles, seven pyroxenes, thirteen blue amphiboles, two green amphiboles, eleven phengites, two paragonites, a mariposite, seven chlorites, and two specimens of albite were obtained from the metamorphic rocks of Île de Groix, and their chemical, physical, optical and X-ray properties determined. The chloritoids are all optically positive, monoclinic polymorphs with large 2V, moderate refractive indices and characterized by high densities. Their fluorine contents have been used to propose a new upper limit for OHF substitution in the chloritoid structure, suggesting that partial pressure of fluorine might modify the stability of chloritoids from that determined in pure H2O. The epidotes belong to the Al-Fe epidote series and are epidote sensu stricto. The almandine-rich garnets and the chloromelanites are metastable relics in the glaucophane schists. The grossular contents of the calcareous schist garnets are believed to have become depressed under high CO2 pressure and the low Tschermak's contents of the pyroxenes are to be explained by equilibria involving epidote at high and low temperature when the Tschermak's components will break down to epidote group minerals. The sphenes contain appreciable amounts of combined water, fluorine substituting for oxygen and aluminium substituting for silicon and titanium. The presence of H3O+ is suspected in a specimen of blue amphibole. The barroisite has a composition between glaucophane and hornblende. On account of its high Fe3+ content it is believed to have formed under higher P O 2 than the blue amphiboles. The paragonites which occur in the ohloritoid veins are unstable in the potassium-rich aluminous schists. The phengites show a tendency towards sericitic composition due to post-glaucophanisation readjustments under the lower pressure conditions of the greenschist facies. Some of the Fe3+ contents of the chlorites are interpreted as due to oxidation of ferrous iron, e.g. 2 [Fe(OH)2]2FeOOH + H2. The minerals show strong chemical control of the host rock and their Mn contents are directly related to those of the minerals from which they have evolved through retrogression.Chloritoids and epidotes that are not associated with garnets contain higher amounts of manganese; similarly, the two blue amphiboles with the highest FeMg ratios were obtained from rocks in which garnet has not appeared. It is therefore believed that ottrelite and piemontite would be stable only at the lowest subfacies of the greenschist facies. Also, the ironrich amphiboles must have evolved from low-grade iron-aluminium chlorites, since on the appearance of garnet in a schist iron-aluminium chlorites react with quartz to give almandine and Mg-rich chlorites. The Fe2+Mg ratios of the blue amphiboles therefore reflect the grade of the original schist in which the minerals formed.  相似文献   

12.
The Cipoeiro gold deposit, located in the Gurupi Belt, northern Brazil, is hosted by tonalites of 2148 Ma. The deposit is controlled by splays related to the major strike-slip Tentugal shear zone, and at the deposit scale, the mineralization is confined to ductile–brittle shear zones. Mineralization style comprises thick quartz veins and narrow and discontinuous quartz-carbonate veinlets associated with disseminations in altered host rocks. The postmetamorphic hydrothermal paragenesis is composed of quartz, calcite, chlorite, white mica (phengite), pyrite, and minor albite. Electron microprobe analysis of chlorites reveals a relatively uniform chemical composition at depths of more than 100 m. The chlorites are characterized by (Fe + Mg) ratios between 0.37 and 0.47 and AlIV ranging between 2.22 and 2.59 a.p.f.u. and are classified as Fe-chlinochlore. Temperatures calculated by applying the AlIV contents of chlorites yield a relatively narrow interval of 305 ± 15°C. Stable isotope (O, H, C, S) compositions have been determined in silicate, carbonate, and sulfide minerals. The δ18O and δD values of the mineralizing fluid range from +2.4 to +5.7 and from −43‰ to −20‰, respectively, and are interpreted as having a metamorphic origin. The δ13C values of fluid CO2 are in the range −10.7‰ to −3.9‰, whereas the fluid δ34S is around 0‰. Carbon and sulfur compositions are not diagnostic of their sources, compatible as they are with mantle, magmatic, or average crustal reservoirs. The hydrothermal paragenesis, chlorite–pyrite coexistence, temperature of ore formation, and sulfur isotope evidence indicate relatively reduced fO2 conditions for the mineralizing fluid. Geologic, chemical, and isotopic characteristics of the Cipoeiro deposit are compatible with the class of orogenic gold deposits.  相似文献   

13.
Five chlorite samples have been studied by 57Fe Mössbauer spectroscopy at different temperatures. The spectra are consistently described by a superposition of one ferric and three ferrous quadrupole doublets. All hyperfine data exhibit only minor variations from sample to sample, meaning that the structural and electronic properties of chlorite are rather insensitive to compositional changes and local cation disorder. Two of the ferrous doublets are ascribed to cis and trans co-ordinations in the T-O-T layers. The third ferrous doublet is interpreted as being due to ferrous ions in the hydroxide sheets. Its hyperfine parameters are close to those of the former doublets and the observed deviations from the parameter values found for pure brucite are discussed. Approximately 20 to 25 percent of the total iron is situated in the hydroxide sheets. All five chlorites contain about 10 percent Fe3+ which is most probably located on octahedral sites. The temperature dependence of the ferrous quadrupole splittings for two chlorites has been interpreted on the basis of the thermal populations of the two lowest electronic states of the Fe2+ ions. From this, the deformations of the different octahedral co-ordinations could be estimated.  相似文献   

14.
Mn-rich members of the pyrosmalite-family [(Mn, Fe)8Si6O15(OH, Cl)10], friedelite and schallerite have been identified as rock-forming minerals together with caryopilite, in several metamorphosed carbonate Mn-deposits. The phase assemblages and mineral compositions are described for eight of these localities each of which represents a distinct geologic situation. Friedelite is always Cl-bearing and occurs both as a prograde phase in low-grade metamorphic rocks (Pyrenees, Haute-Maurienne) and as a secondary phase formed by retrogressive replacement of primary anhydrous phases in higher-grade rocks. Schallerite, an Asbearing relative of friedelite, occurs in the greenschist metamorphic deposit of the Ködnitztal (Austria) together with other As-minerals. In these deposits, caryopilite is typically formed during retrograde metamorphism by alteration of, generally anhydrous, Mn-silicates. Based upon these occurrences, a qualitative petrogenetic grid for the system MnO-SiO2-CO2-H2O with the phases friedelite, caryopilite, pyroxmangite/rhodonite, tephroite, rhodochrosite, quartz, CO2, and H2O is proposed. The phase relations imply that Cl- (or As-) free friedelite is not stable in hydrous systems with respect to caryopilite. From the mineral assemblages containing hydrous Mn silicates, waterrich fluids are inferred during the retrograde metamorphic evolution of the investigated deposits. Chemical data for Mn-rich chlorites, which are basically members of the clinochlore-pennantite series which coexist with the pyrosmalite minerals, show the absence of intermediate Mn/Mg ratios. This supports the existence of a miscibility gap as previously hypothesized by other authors.  相似文献   

15.
粘土矿物组合和绿泥石成分常被用来讨论盆地沉积物的成岩作用和埋藏古温度。许多沉积盆地的研究结果显示,泥 岩和页岩中的粘土矿物组合和绿泥石的成分与埋藏深度/温度有关。但也见有例外的现象存在。文中主要探讨了新疆塔北隆 起泥岩中的粘土矿物组合和绿泥石成分的特征,以及与盆地古盐度的关系。研究结果表明：（1）在塔北隆起泥岩中,埋藏 深度2777.37~4604.41m,地层单位为J1-N2的粘土矿物组合为I+Chl和I+Chl+Ka; 埋藏深度5071.52~5299.37m,地层单位为 T1的粘土矿物组合为R0I/S+I+Chl和R0I/S+Chl。（2）研究区的成岩绿泥石为Ⅱb型铁镁绿泥石,其成分特征主要表现为： ①配位八面体中阳离子的占位数为11.532(总平均值);②ⅥAl含量明显大于ⅣAl含量;③（Fe+Mg）为4.016（总平均值）;④ Si/Al比值>1。（3）根据研究区盐类矿物的分布范围以及古盐度的数据,讨论了古盐度对该区粘土矿物组合和绿泥石成分的 影响,指出古盐度是影响本区粘土矿物组合和绿泥石成分变化的主要因素。用古盐度解释了<5000m深度的粘土矿物组合 中不含无序伊/蒙混层（R0I/S）矿物,而>5000m深度粘土矿物组合中含有无序伊/蒙混层（R0I/S）矿物的异常现象。揭示了 在一定的深度范围（2777.37~4405.27m）,一定的古盐度条件下（Sr/Ba比值≥0.4,并有盐类矿物出现）,绿泥石成分受到 古盐度的制约,并且随着古盐度的增高,绿泥石成分中的Al、ⅣAl、Na、Na2O、Al/Si随之增高,而Si/Al则随之降低。由 绿泥石成分温度计获得的温度值也伴随着古盐度的增高而增高。因此,由绿泥石成分温度计所计算的温度不能代表本区实 际埋藏的古温度。（4）研究区内绿泥石成分中的SiO2和FeO与母岩的对应成分之间有一定的相关性,其SiO2绿泥石与SiO2岩石、 FeO绿泥石与FeO岩石呈负相关的线性关系,并且这种关系在古盐度的干扰下也未受到影响。  相似文献   

16.
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&amp) < 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   

17.
Harzburgite and lherzolite tectonites from the Horoman peridotite complex, Hokkaido, northern Japan, contain variable amounts of secondary phlogopite and amphibole. Phlogopite-rich veinlets parallel to the foliation planes usually cut olivine-rich parts of the rocks; single-grained interstitial phlogopites are usually associated with orthopyroxene grains. Amphiboles are disseminated in rocks or sometimes occur in the phlogopite-rich veinlets. Within individual veinlets, phlogopites show extensive inter-grain variations in K/(K + Na) ratio (0.96–0.75), generally decreasing from the central (usually the thickest) part towards the marginal parts of veinlets. In contrast, Ti contents are nearly constant in Ti-poor veins or decrease slightly with decreasing K/(K + Na) in T-rich veins. Variation of Ti in phlogopites is very large (0.1–6.8 wt%) and is inversely correlated with Mg/(Mg + Fe*) (Fe*, total iron) atomic ratios, which vary from 0.96 to 0.88. Intra-vein variation of phlogopite chemistry (especially K/(K + Na) ratio) could be achieved by in situ fractional crystallization of trapped fluids; variation of Ti, however, cannot be explained by in situ fractionation of the fluids, indicating various Ti contents of the parent fluids. It is suggested that fluids responsible for the formation of the Horoman phlogopites and amphiboles were magmatic volatiles successively released from evolving alkali basaltic magmas. Individual fluids trapped within peridotites were fractionated, precipitating phlogopites successively poorer in K. When the fluids became rich enough in Na, amphiboles co-precipitated with phlogopites. Similar fractional crystallization of phlogopites and amphiboles is expected in the upper mantle on a larger scale if fluids move upwards. This process may control, at least partly, a lateral K/Na distribution in the upper mantle; K and Na may be concentrated in deeper and shallower parts, respectively.  相似文献   

18.
Chlorite constitutes a major hydrothermal alteration product of metamorphism of andesites, in the active geothermal system of Los Azufres (Mexico). Electron microprobe analyses performed on a set of crystals from each sample show wide variations in composition. Correlation coefficients among chemical constituents were calculated. It is shown that the tetrahedral charge is positively correlated with the octahedral vacancy and negatively with the iron content, and there is almost no correlation with the octahedral aluminium and magnesium content. A procedure is proposed to select end-members and substitution vectors, and to give a general formula for these chlorites.Their formation temperatures are estimated with great accuracy, combining results of microthermometric data on fluid inclusions from gangue minerals of chlorites (quartz, calcite), direct measurements in wells (Kuster equipment), and chemical geothermometers. Correlations between chlorite compositions, range and nature of site occupancy, and temperature are good. Formation temperatures of chlorites range from 130° C to 300° C. As no other thermodynamic parameter varies significantly in the studied field (composition of the host rocks, nature of the geothermal fluids, pressure, ...), these variations of site occupancy (mainly Al(IV) and the octahedral occupancy (6-Al(VI)-(Mg+Fe(2+)) = VAC) are considered mainly as temperature dependent.Molar fractions of each end-member show very different variations with increasing temperature: X-kaolinite decreases, and X-chamosite increases, while X-talc-3 brucite does not show significant change. From these data, activity coefficients and standard state chemical potential of major components, and molar free energy formation of chlorite have been calculated for each temperature of crystallisation.  相似文献   

19.
Nickel mineralisation occurs in shears in Archaean serpentinised peridotite near Nullagine, Western Australia. The principal nickel minerals are millerite, polydymite and pecoraite, which occur chiefly as concentrations of nodular grains, mostly between 1 and 5 mm in diameter. The polydymite represents a replacement of millerite, and is in turn partly replaced by gaspéite. The pecoraite grains generally contain several percent chromium, and are frequently rimmed by millerite‐containing magnetite. A similar type of nodule consists of nullaginite (Ni2(OH)2CO3). Other major minerals in the shears include various types of serpentine and magnesite, coarse chlorite, and apatite. The assemblage is cut by late veinlets of gaspéite, pecoraite, otwayite (Ni2(OH)2CO3.H2O), and nullaginite. Trace amounts of barite, cinnabar, parkerite, shandite, breithauptite, and nickeloan greenockite are also present.

The bulk of the mineralisation is attributed to the effects of hydrothermal and/or metasomatic activity along shears in the serpentine. Concretionary magnesite in some of the shears is believed to be the result of Tertiary weathering. The late veinlets of nickel minerals and the replacement of millerite and polydymite are attributed to supergene effects.  相似文献   

20.
The composition of minerals of the titanite-malayaite series and their mineral assemblages and genesis were examined at the Bol’shoi Kan’on deposit in Magadan oblast and at other deposits. These minerals were demonstrated to be typomorphic Sn-bearing silicates in postmagmatic bimetasomatic hypabyssal calc skarns and skarnoids in tin-bearing provinces. The series of these minerals with similar crystal structures has a miscibility gap, and the minerals are characterized by notably different Sn concentrations. Moreover, titanite may contain Al, Fe, F, and OH, whose concentrations decrease in the Sn-bearing members of the series (malayaite). These silicates were formed at many deposits after the successive transforms of skarn mineral assemblages. The early assemblages include wollastonite in calcic carbonate rocks and diopside and salite in skarnoids. The latter minerals are replaced first by hedenbergite with subordinate amounts of vesuvianite and garnet first of grossular and then andradite composition. This process was syngenetic with the formation of borosilicates (danburite, axinite, and tourmaline). Ti thereby may be accommodated in grossular and Sn in Fe-bearing silicates, mostly, in andradite. Skarns often contain both titanite and malayaite, which were produced in these rocks earlier than cassiterite. The isomorphic series of these minerals has a miscibility gap. The oreforming processes ended with the crystallization of quartz, fluorite, and rare sulfides, including stannite. The late Sn-bearing minerals at some deposits are stokesite and Mg, Fe, and Ca stannates, which crystallized during malayaite replacement by newly formed calcite-quartz aggregates. The Sn-bearing sulfides are replaced by varlamoffite during supergene processes.  相似文献   

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