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1.
Summary ?The Yunlong tin deposit is located in the northern part of the Lancangjiang metamorphic zone of the Sanjiang Tethys orogen series in western Yunan province of China. It consists of vein-type cassiterite ores, which are mainly hosted in migmatites of Caledonian age. Abundant tourmaline is associated with the ores, quartz–tourmaline veins and barren migmatized gneiss and migmatites. A detailed electron microprobe study has been carried out to document the chemical compositions of tourmaline from this deposit. The results exhibit a systematic compositional change that might be used as tracer for ore genesis and in prospecting for tin mineralization. Tourmalines from the ore bodies are dravite with Fe/(Fe + Mg) ratios of 0.09 ∼ 0.31 and Ca/(Ca + Na) ratios of 0.03 ∼ 0.40. These tourmalines are also rich in chromium (up to 0.74 wt% Cr2O3) and tin (up to 0.42 wt% Sn). In contrast, tourmalines from the barren migmatites are mostly schorl with Fe/(Fe + Mg) ratios of 0.38 ∼ 0.94 and Ca/(Ca + Na) ratios of 0.00 ∼ 0.14. Tourmalines from quartz–tourmaline veins that occur between ore bodies and the migmatites show intermediate compositions, i.e., Fe/(Fe + Mg) = 0.09 ∼ 0.59, Ca/(Ca + Na) = 0.01 ∼ 0.22. It is suggested that the Mg-rich nature of the tourmaline can be used as an exploration tool in this region to target tin mineralization, because the tourmalines show increasing Mg contents and are more dravitic when approaching the ore bodies. It is likely that the formation of the Yunlong tin deposit was related to migmatitic-hydrothermal processes. The high Mg and Cr contents in tourmalines from the ore bodies were probably derived from the local meta-sedimentary and meta-volcanic rocks of the Precambian Chongshan Group rather than from the granites in the region. Received December 28, 2000; revised version accepted January 25, 2002  相似文献   

2.
Zoned tourmaline（schorl-dravite） in the matrix of hydrothermal explosive breccia and ore veins in gold deposits,Chita region.Eastern Transbaikalia.Russia,are associated with Na- and K-rich porphyry-type subvolcanic intrusives.δ18O values of tourmaline from three gold deposits（Darasun. Talatui,Teremkinskoye） are +8.3‰,+7.6‰,and +6.0‰and calculatedδ18O values of fluids responsible for the tourmalinization are +7.3‰,+7.7‰,and +4.2‰,respectively.These data imply an igneous fluid source,except at the Teremkin deposit where mixing with meteoric water is indicated.Wide ranges of Fe3+/Fetot,and the presence of vacancies characterize the Darasun deposit tourmaline indicating wide ranges of f（O2） and pH of mineralizing fluids.Initial stage tourmalines from the gold deposits of the Darasun ore district are dravite or high mg schorl.Second stage tourmaline is characterized by oscillatory zoning but with Fe generally increasing towards crystal rims indicating decreasing temperature.Third stage tourmaline formed unzoned crystals with xMg（mole fraction of Mg） close to that of the hrst stage tourmaline,due to a close association with pyrite and arsenopyrite.From Fe3+/Fetot values,chemical composition and crystallization temperatures.logf（O2） of mineralizing fluids ranged from ca.—25 to—20. much higher than for the gold-bearing beresite—listvenite association,indicating that tourmalinization was not related to gold mineralization.  相似文献   

3.
广西大厂地区笼箱盖黑云母花岗岩与区内晚白垩世锡多金属成矿作用在时空上密切相关。岩相学特征表明,笼箱盖黑云母花岗岩中的电气石可以分为三类:1)浸染状电气石; 2)石英-电气石囊; 3)电气石-石英脉。本文利用电子探针和激光剥蚀等离子体质谱系统测定三种不同产状电气石的化学组成。分析结果显示,三种产状的电气石均具有高的Fe/(Fe+Mg)和Na/(Na+Ca)比值,主体属于碱基亚类铁电气石。浸染状电气石为岩浆晚期结晶,其Fe/(Fe+Mg)比值变化于0. 85～0. 94,随着岩浆分异,电气石逐渐富集Li、F、Fe和Sn等元素。与浸染状电气石相比,石英-电气石囊中早阶段电气石具有低的Fe/(Fe+Mg)比值,高的V、Co和Sr含量,可能反映了岩浆演化晚期出现的不混溶富硼熔/流体对早期黑云母和长石的交代作用,从而使囊中早阶段电气石继承部分被交代矿物的化学组成特征;石英-电气石囊中晚阶段电气石的化学组成变化较大(如Li、F、Mg、Al、V、Fe和Zn),与热液成因电气石的推论一致。与浸染状和囊状电气石相比,石英脉中的电气石具有高的Fe/(Fe+Mg)和Na/(Na+Ca)比值;微量元素组成与囊状电气石相似。就成矿元素锡而言,三种产状的电气石均具有相对高的锡含量,与其他地区锡成矿花岗岩中电气石的成分特征相似。但是,从岩浆晚期到热液阶段,大厂地区电气石的锡含量并没有显著升高,可能反映了早期岩浆热液流体对熔体锡有限的萃取作用。  相似文献   

4.
Tourmaline in Proterozoic Massive Sulfide Deposits from Rajasthan, India   总被引：1，自引：0，他引：1  
We have analyzed the chemical composition and boron isotope composition of tourmaline from tourmalinites, granite and a quartz-tourmaline vein from the Deri ore zone and from a pegmatitic band in the Rampura-Agucha ore body. These two Proterozoic massive sulfide deposits occur in the Aravalli-Delhi orogenic belt, Rajasthan, northwest India. Tourmaline from stratiform tourmalinites closely associated with the massive sulfides in the Deri deposit have preserved their original chemical compositions despite regional and thermal metamorphism in the area. These tourmalines have low Fe/(Fe + Mg) ratios (0.19–0.30; mean 0.26) that suggest formation close to the sediment-sea water interface. The δ11B values (−15.5 and −16.4‰) are compatible with boron derived from leaching of argillaceous sediments and/or felsic volcanics underlying the original massive sulfide deposit during its formation. Boron isotope compositions measured in tourmaline from a post-ore granite and quartz-tourmaline vein in the Deri deposit indicate that boron in these tourmalines was derived from the tourmalinites produced during ore formation. The boron isotope systematics of a coarse brown tourmaline crystal from a pegmatitic band on the hanging wall contact of the Rampura-Agucha deposit indicate that 45 ± 25% of the boron within the original tourmaline was lost during upper amphibolite facies regional metamorphism. Received: 3 April 1996 / Accepted: 11 April 1996  相似文献   

5.
《Chemical Geology》1992,94(3):215-227
Tourmaline is a ubiquitous mineral in the Mid-Proterozoic, peraluminous, syn- to post-tectonic granites and aplites and the related hydrothermal rocks of the Karagwe-Ankolean belt in northwest Tanzania. Electron microprobe analysis indicates that tourmalines from all of the intrusive and hydrothermal lithologies: (1) belong to the schorl-dravite solid-solution series; and (2) plot within the field occupied by tourmaline from Li-poor granitoids on the Fe-Al-Mg classification diagram. Oxygen isotope compositions range from +12.2 to +11.6‰ (SMOW) for magmatic tourmalines and from +10.8 to +9.8‰ for those of hydrothermal origin. Hydrogen isotope compositions vary from −79 to − 65‰ (SMOW) for magmatic tourmalines and from −99 to −84‰ for hydrothermal tourmalines. Water contents measured by manometry are constant at 3.0–3.2 wt.%. Within the broad grouping there arc systematic variations in both chemical [particularly Fetot/(Fetot + Mg ratio)] and isotopic composition that relate to evolving magmatic and hydrothermal conditions. Igneous differentiation [increasing Fetot/(Fetot + Mg) in magmatic tourmaline] has produced trends with higher δ18O in quartz, lower δ18O in tourmaline, and larger ΔQTZ.−TOUR.-values, that reflect a combination of a reduction of crystallization temperature and an increase of Fetot/ (Fetot + Mg) in the residual melt. Subsequent cooling and interaction of an exsolved, B-rich magmatic fluid with the pelitic country rocks, resulted in the deposition of hydrothermal tourmaline with increasing Fetot/(Fetot + Mg) ratios, and progressively lower δ18O and δD -values.  相似文献   

6.
祖母绿是由微量Cr和/或V致色的绿色绿柱石。位于云南省麻栗坡县的大丫口祖母绿矿床是中国重要的祖母绿矿床,近年来取得了一系列的研究进展,但与祖母绿相关的电气石的研究工作还未展开。本文以大丫口矿床含祖母绿矿脉和非矿脉中的电气石为研究对象,在详细的野外调查和岩相学研究基础上,对电气石进行成分测试,旨在探讨电气石成因、查明物质来源和流体演化过程,进一步探究大丫口祖母绿矿床的成矿机制。结果显示:含矿脉电气石单位分子中Na含量为0.62~0.79 apfu,Al含量为5.36~6.17 apfu,Fe/(Fe+Mg)值为0.31~0.41;非矿脉电气石单位分子中Na含量为0.64~0.76 apfu,Al含量为5.66~6.38 apfu,Fe/(Fe+Mg)值为0.14~0.34。大丫口电气石具有富Mg、Y位(Y-site)上呈低Al或无Al的特征,属于碱族镁电气石,但是含矿脉电气石则显示更高的Fe/(Fe+Mg)值。电气石成分的差异可能主要与形成环境有关,电气石的成分差异具有指示祖母绿是否富集的潜力。大丫口电气石具有成分分带且V2O3含量为0.65%~4.76%,其形成与持续的热液流体交代围岩有关。大丫口矿床是一个岩浆起源的动态热液体系,流体通过碱交代作用参与水岩反应萃取围岩中的成矿物质。早期流体的物质组成以源于花岗质熔体的Si、Al、Be、F、P为主,而随着演化的进行,Ca、V等来自地层的成分逐渐增加。研究表明,铍的氟化物或氟铍络合物是大丫口成矿流体中Be的一种重要的迁移方式。萤石、氟磷灰石等含氟矿物的结晶促使铍的氟化物或氟铍络合物分解,流体中氟元素的减少可能是大丫口祖母绿成矿的重要机制之一。  相似文献   

7.
辽东裂谷带硫化物矿床内电气石系列矿物学与找矿关系   总被引：5，自引：0，他引：5  
本文通过辽东裂谷硫化物矿床中不同产状电气石的研究，提示了不同环境内形成电气石矿物的标型、光性、成分、同位素组成、红外光谱与Ｘ衍射特征方面存在一定差异。不同物化条件下形成的电气石其演化系列表现在由近矿围岩到硫化物矿层电气石由富镁由富铁－镁过渡从层状矿体到热液改造矿体电气石由铁镁向富钙－镁过渡。研究表明，电气石的形成与元古代早期底火山喷发作用后引起的富硼热泉活动有关。  相似文献   

8.
The Bamble sector of southern Norway comprises metagabbros and metasediments that were metasomatically altered to various extents during a late stage of the Sveconorwegian orogeny (~1.06 Ga). The infiltration of highly saline brines along veins led to penetrative scapolitization and albitization on a regional scale and the local deposition of Fe–Ti oxides. Typical secondary mineral assemblages include either scapolite + apatite + amphibole + phlogopite + tourmaline, or albite + epidote + calcite + chlorite + white mica, indicating that the fluids introduced large amounts of Na, Cl, Mg, Ca, K, P, and B to the system. Metasomatic tourmalines associated with different alteration stages as identified by variations in major-element composition and initial 87Sr/86Sr were analyzed for B isotopic compositions to constrain possible sources and the evolution of the hydrothermal fluid(s). Measured δ11B values range from ?5 to +27 ‰ relative to SRM-951, suggesting marine evaporites interlayered with various amounts of continental detritus and pelagic clay as a possible B source reservoir. The influence of a seawater-derived component is clearly indicated by the heavy B isotope signature of tourmaline related to Al–Mg-rich metapelites. In contrast, negative δ11B values can be explained by the influence of pneumatolytic fluids associated with granitic pegmatites. On a regional scale (i.e., several km), δ11B values in tourmaline vary widely, whereas variations within a single outcrop (tens of m) are typically small and can be ascribed to different generations of tourmaline related to several fluid pulses.  相似文献   

9.
Tourmaline is widespread in metapelites and pegmatites from the Neoproterozoic Damara Belt, which form the basement and potential source rocks of the Cretaceous Erongo granite. This study traces the B-isotope variations in tourmalines from the basement, from the Erongo granite and from its hydrothermal stage. Tourmalines from the basement are alkali-deficient schorl-dravites, with B-isotope ratios typical for continental crust (δ11B average −8.4‰ ± 1.4, n = 11; one sample at −13‰, n = 2). Virtually all tourmaline in the Erongo granite occurs in distinctive tourmaline-quartz orbicules. This “main-stage” tourmaline is alkali-deficient schorl (20–30% X-site vacancy, Fe/(Fe + Mg) 0.8–1), with uniform B-isotope compositions (δ11B −8.7‰ ± 1.5, n = 49) that are indistinguishable from the basement average, suggesting that boron was derived from anatexis of the local basement rocks with no significant shift in isotopic composition. Secondary, hydrothermal tourmaline in the granite has a bimodal B-isotope distribution with one peak at about −9‰, like the main-stage tourmaline, and a second at −2‰. We propose that the tourmaline-rich orbicules formed late in the crystallization history from an immiscible Na–B–Fe-rich hydrous melt. The massive precipitation of orbicular tourmaline nearly exhausted the melt in boron and the shift of δ11B to −2‰ in secondary tourmaline can be explained by Rayleigh fractionation after about 90% B-depletion in the residual fluid. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

10.
The c. 1.9 Ga old Stollberg sulphide and Mnrich skarn iron ores and sulphide ores in Bergslagen, south-central Sweden are hosted by hydrothermally altered and metamorphosed felsic volcanic and volcaniclastic rocks. The ores are underlain by comformable alteration zones characterized by albite-gedrite-quartz and biotite-muscovite-plagioclase-K-feldspar-quartz +/– garnet assemblages. The present mineralogies are interpreted as medium-grade metamorphic equivalents to the original alteration mineral assemblages. PT-conditions during prograde regional metamorphism are semiquantatively determined to be 510 to 560 °C at approximately 3 kbar. With increasing modal content of gedrite and biotite in the alteration zones, the Mg/Fe ratios and XMg's in octahedral positions of these minerals also increase. In the gedrite-bearing strata, whole-rock Mg/Fe ratios remain constant, whereas in the biotite-rich unit the wholerock Mg/Fe trend is parallel to that of the biotites.The trends in the metamorphic mineral composition are interpreted to be a product of original changes in fluid composition during the evolution of a sub-seafloor hydrothermal system. During the initial stage of alteration, Fe-Mn-rich fluids altered the rocks, and during a later stage, the fluids became more Mg-rich, possibly due to entrainment of fresh seawater, and the alteration zones became relatively more Mg-rich. Sulphide precipitation was contemperaneous with Mg metasomatism, suggesting base metal precipitation was a function of the mixing of cool seawater with hydrothermal fluid. It is proposed that early hydrothermal alteration was associated with the deposition of areally extensive Fe-oxide formation, and that Mg metasomatism defines a second stage of hydrothermal activity during which sulphide mineralization overprinted the earlier formed Fe-oxide deposit.  相似文献   

11.
加拿大Sullivan矿床是世界上最典型的SEDEX型Pb-Zn-Ag矿床。对该矿床中产出的几个特征矿物,如硼矿物电气石,富氯的方柱石和黑云母,富钡的钾长石和白云母,及富锰的石榴子石、绿泥石、碳酸盐和钛铁矿进行了研究。指出这些矿物的存在反映了该矿床产出的物理化学环境。提出成矿流体可能淋滤了深部存在的非海相蒸发岩层,层状硫化物矿石可能形成于海底高盐度热卤水池中。  相似文献   

12.
山西省中条山铜矿田电气石与电气石岩的研究   总被引：4，自引：0，他引：4       下载免费PDF全文
本文通过对中条山铜矿田电气石和电气石岩地质产状、岩相学和矿物学、矿物化学等特征的研究，指出本区有三种成因类型的电气石：（１）北峪酸性侵入体岩浆期后热液成因电气石；（２）中条群地层中变质热液形成的电气石；（３）赋矿岩石和近矿围岩中热液蚀变电气石。第（３）类电气石具有特征的产状、矿物化学和矿物共生组合标型，是重要的找矿标志  相似文献   

13.
Tourmalinites that are distally associated with tungsten deposits of the Pampa del Tamboreo area, San Luis, Argentina, contain tourmalines retaining evidence for its origin and evolution. Tourmaline grains uncommonly contain small grains of detrital tourmaline. Analysis of a single detrital tourmaline grain reveals that it is a Ca-rich “oxy-dravite”. Proximal to the detrital cores there are inner domains of asymmetric tourmaline overgrowths that developed during low grade metamorphism. Volumetrically dominant tourmaline overgrowths in the outer domain are concentrically zoned aluminous dravite and “oxy-dravite” with Al/(Al + Fe + Mg) = 0.71–0.74 and Mg/(Mg + Fe) = 0.64–0.71. Variability of Al is primarily controlled by the deprotonation substitution R + OH− = Al + O2− (where R = Fe + Mg), and is a function of the activity of H2O. A likely evolutionary scenario is one in which volcanogenic material is altered by hydrothermal fluids in the sea floor resulting in an aluminous and magnesian residuum. With further hydrothermal circulation and incipient metamorphism, boron-rich fluids are expelled from metasedimentary and metavolcanic basement rocks and develop Mg-rich tourmalinites in the aluminous, magnesian host rocks. The tourmalinization process occurs over a range of metamorphic conditions and with fluids of variable activity of H2O.  相似文献   

14.
Petrographic and chemical criteria indicate that the overwhelming majority of olivines in kimberlites are probably cognate phenocrysts. The implied low volume of xenocryst olivines requires that primitive kimberlite magmas are highly ultrabasic liquids. Two chemically distinctive olivine populations are present in all of the kimberlites studied. The dominant olivine population, which includes large rounded olivines and smaller euhedral crystals, is Mg-rich relative to late-stage rim compositions. It is characterized by a range in 100 Mg/(Mg + Fe) and uniform Ni concentration, reflecting Rayleigh-type crystallization during magma evolution. The most Mg-rich of these olivines are considered to be similiar to those in the mantle source rocks. The second compositional population, generally very subordinate, though markedly more abundant in the megacrystrich Monastery kimberlite, is Fe-rich relative to rim compositions. This group of olivines crystallized from evolved liquids in equilibrium with iron-rich megacrysts, both entrained by the kimberlite magma during ascent. Differences between the chemical fields of Fe-rich olivines in Group I and Group II kimberlites point to relatively deeper derivation of the latter suite. Olivine chemistry can be used to characterize kimberlite magma sub-types, and may prove to be a useful tool for evaluating the diamond potential of kimberlites.  相似文献   

15.
Abstract: The Gejiu tin polymetallic deposits are located in the southeastern part of Yunnan Province in China. A detailed electronic microprobe study has been carried out to document geochemical compositions of tourmalines from the deposits. The results indicate a systematic change of mineral geochemical compositions, which might be used as a mineral geochemical tracer for post-magmatic hydrothermal fluid, basin fluid and their mixture. The tourmalines from granite are schorl with Fe/(Fe+Mg) ratios of 0.912-1.00 and Na/(Na+Ca) ratios of 0.892-0.981. Tourmalines as an inclusion in quartz from the ore bodies are dravite with Fe/(Fe+Mg) ratios of 0.212-0.519 and Na/ (Na+Ca) ratios of 0.786-0.997. Tourmalines from the country rocks are dravite with Fe/(Fe+Mg) ratios of 0.313-0.337 and Na/(Na+Ca) ratio of 0.599-0.723. Tourmalines from cassiterite-tourmaline veins that occur in crannies within the country rocks show distinct optical zoning with alternate occurrence of dravite and schorl, Fe/(Fe+Mg)=0.374-0.843, Na/(Na+Ca)=0.538-0.987. It suggests that schorl in granite and dravite in carbonatite are related to magmatic fluid and basin fluid respectively. When magmatic fluid rose up and entered into crannies of the country rocks, consisting mainly of carbonatite, basin fluid would be constantly added to the magmatic fluid. The two types of fluid were mixed in structural crannies of the sedimentary basin accompanied with periodic geochemical oscillations to form material records in chemical composition zonings of tourmalines.  相似文献   

16.
Tourmaline-rich rocks associated with clastic metasedimentary rocks of Carboniferous age occur in the Cinco Villas massif, western Pyrenees. Three types of tourmaline-rich rocks were distinguished: (1) Fine-grained stratiform tourmaline-rich rocks, which are associated with carbonaceous metapelites (TR1); (2) stratabound tourmaline-rich rocks, associated with metapelites in the contact aureole of the Aya granitoid pluton (TR2); (3) stratabound to massive tourmaline-rich rocks, associated with psammopelites in contact with granites and pegmatites (TR3). Tourmalines belong to the schorl–dravite solid solution series and have a wide compositional range, from nearly end-member dravite for TR1 tourmalines to schorl for TR3 tourmalines; TR2 tourmalines have intermediate compositions. The Fe/(Fe+Mg) typically varies between 0.02 and ≈0.55, increasing from TR1 to TR3. The TR1 tourmalines commonly display a discontinuous chemical zoning with Fe-rich green cores (8–8.5% FeO) and Mg-rich colorless rims (10–11% MgO). In contrast, crystals that exhibit fine growth lamellae appear to lack significant chemical zoning. Oxygen and hydrogen isotope compositions also reveal major differences between TR1 and TR3 tourmalines, the former displaying heavier δ18O values (17.7–19‰) and δD values (−35 to −42‰) than TR3 tourmalines 11 to 13‰ and −47 to −76‰, respectively. The TR2 tourmalines show intermediate values of 11.3 to 14.6‰ for δ18O and −40 to −55‰ for δD. Linear and continuous chemical variations obtained for major and trace elements of the whole rocks reflect mixing between clay-rich and quartz-rich end-members, indicative that some tourmaline-rich rocks contain a significant detrital component. Chondrite normalized REE (rare earth element) patterns of tourmaline-rich rocks are similar to those of surrounding unaltered clastic metasediments, except for some TR1 rocks which are characterized by low contents of ΣREE. Mass-balance calculations show that tourmaline-forming processes plus metamorphism led to mass and volume changes at mesoscopic scales (≈10% for the TR1 tourmalinites). Silicon, Fe, Mn, and REE elements were partially lost from sedimentary rocks, whereas Mg and particularly B were added to pelitic sediments. Available data, nevertheless, do not allow an assessment of the boron source. Formation of the TR1 tourmaline-rich rocks probably was the net result of several processes, including direct precipitation from B-rich hydrothermal fluids or colloids, early diagenetic reactions of carbonaceous pelitic sediments with these fluids, and subsequent recrystallization during regional metamorphism. The TR2 tourmaline-rich rocks mainly developed by metamorphic recrystallization of TR1. Tourmaline-rich rocks and veins adjacent to pegmatites and granitic rocks (TR3) are the result of boron metasomatism; the primary boron having been recycled from stratiform tourmalinites during regional metamorphism and magmatism. Received: 18 November 1996 / Accepted: 25 April 1997  相似文献   

17.
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   

18.
Euhedral dissakisites from Trimouns dolomite mine, France, is compositionally zoned. Back-scattered electron (BSE) images reveal that each of the described dissakisite crystals has three distinct compositional zones: normal zoned core (Mg-rich), oscillatory zoned middle (Ca–Al-rich) and homogeneous rim (Fe–ΣREE-rich). The latter zone with Fe2+ > Mg corresponds to allanite-(Ce). Dissakisite-(Ce) also displays pronounced zoning in Fe/Mg which may suggest that the temperature of crystallization continuously decreased from core to rim. Despite a systematic increase in Fe/Mg of the dissakisite with an allanite rim, there is no monotonic decrease in the REE zoning: the normal zoned core and homogeneous rim are rich in La, Ce and Pr, but the relatively REE-poor oscillatory zoned middle is relatively abundant in Y, Sm and Gd. Discontinuous variation in REE content of the dissakisite, with the allanite rim may indicate a localized change in either the relative concentration of various ligands or pH of the crystallizing fluid. Observations under the polarizing microscope confirm that the different zones have simultaneous extinction. These chemical and optical observations suggest that epitaxial crystallization of dissakisite, from Trimouns, passes through three formation stages. The ternary Fe2+–Mg2+–(Al + Fe)3+ diagram illustrates that in general dissakisite can be classified into two groups, (Al + Fe)3+-rich and an Mg-rich; dissakisite from Trimouns belongs to the former group. Chondrite-normalized REE patterns of dissakisites from Trimouns are similar to those of allanites formed by hydrothermal fluids. In conclusion, it is clear from the above two geochemical characteristics that dissakisites from Trimouns are of (Al + Fe)3+-type, and were derived from hydrothermal fluids.  相似文献   

19.
Hydrothermal fluid evolution north of the St Austell granite,southwest England, has been studied through geochemical analysisof tourmaline from a fault breccia of <2 cm width withinmassive quartz–tourmaline rocks at Roche. Brecciated tourmalinegrains have overgrowths of <400 µm width [Fe/(Fe +Mg) = 0·31–0·99] with four chemically distinctzones (1–4, towards the margins). Variations in overgrowthcomposition were caused by episodic mixing between Mg-, Al-richmagmatic hydrothermal fluids (dominant in zone 1), with an increasingcomponent of more oxidizing, Fe-rich formation waters (zones2 and 4). More oxidizing conditions are supported by high Sncontents in zone 2 (<0·35 wt %), with Sn probablypresent as Sn4+ rather than Sn2+, the usual form in hydrothermalfluids. From X-ray maps, zones 1 and 3 occur exclusively asovergrowths on pre-existing grains, indicating that overgrowthformation was kinetically favoured over tourmaline nucleation.In zones 2 and 4, nucleation and growth occurred, possibly asa result of supersaturation with respect to tourmaline duringincreased mixing with formation waters. Tourmaline is associatedwith the main episode of mineralization in many important mineraldeposits, often unaffected by alteration. This method of studyinghydrothermal fluid evolution may therefore have uses in exploration,particularly for tourmaline-breccia-hosted ores in Cu-porphyrydeposits. KEY WORDS: breccia; Cornwall; hydrothermal; tin; tourmaline  相似文献   

20.
The San Jorge porphyry copper deposit in Mendoza, Argentina in some parts contains breccia pipes that are strongly enriched with tourmaline of the dravite–schorl solid solution series with some quartz, muscovite, orthoclase, kaolinite, Cu sulfides and arsenopyrite. The overall composition of tourmaline is rather homogeneous with an intracrystalline variation of the Fe/Mg ratio reflected by its texture, its core-rim zonation of tourmaline and by the statistical variation of the Fe/Mg ratio. The depth-related intracrystalline changes are best interpreted as a hydrothermal collapse breccia which formed as a result of the reaction of primary hydrothermal B–Fe-enriched fluids with the country rocks enriched in Mg. The chemical composition attests to only small-scale interaction of tourmaline with silicate fragments within the tourmaline breccia itself. Tourmaline as one of the ultrastable heavy minerals in stream sediment offers a potential tool to discriminate between Cu-bearing and barren breccia pipes, using the Fe/Mg ratio of the boron silicate for distinction. Fertile breccias reveal a significantly better correlation between Fe and Mg than barren tourmaline breccias.  相似文献   

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