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1.
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   

2.
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   

3.
许虹  彭齐鸣  Martin  R.  Palmer 《中国地质》2004,31(3):240-253
辽宁东部古元古界底部地层(南辽河群)中赋存着大型的硼酸盐矿床，含矿层位中广泛分布含电气石的变粒岩和电英岩。空间上这些含电气石的岩石与硼酸盐有着密切的联系，电气石可以作为区域硼矿找矿的标志。已有研究结果表明，该地区的硼酸盐矿床是变质蒸发岩成因。本研究对该区不同产状的电气石和硼酸盐的地质特征，全岩和矿物成分、硼同位素组成进行了分析。本区的电气石包括层状和脉状两大类，而电气石的富集与硼酸盐关系密切，电英岩往往分布在硼酸盐矿体的上盘。而矿体的下盘一般不产出富电气石的岩石。当长英质脉体穿过硼酸盐矿体时，脉体中往往会富集电气石。含电气石岩石的全岩地球化学分析表明，它们的REE及其他微量元素特征以及相关性关系与周围不含电气石的同类岩石十分相似，反映出一种成因上的联系。本区电气石主要属于镁电气石一铁电气石系列，靠近硼矿体的电气石比远离硼矿体的电气石更加富镁，有着更高的Mg／Fe比值。电气石和硼酸盐的硼同位素成分分析显示出二者在同位素组成上的相似性，前者比后者的δ^11B稍低，这可能是由于热液活动过程中同位素分馏的结果。电气石的硼同位素组成在空间上显示出变化规律：远离硼酸盐矿体的电气石的δ^11B值(-5．2‰- 3．6‰)比矿体附近的电气石低(平均 10．5‰)。以上空间和成分上的关系表明硼酸盐可能是形成电气石主要的硼来源，电气石是在热液过程中通过淋滤下伏含硼蒸发岩中的硼形成含硼热液，在与上覆沉积物交代过程中形成含电气石岩石。电气石的条带是热液顺层选择交代的结果。本区电气石与硼酸盐的关系表明，层状电气石可以通过含硼热液交代的方式形成。变质地体中的层状电气石岩石的出现可能与变质蒸发岩有关。这一认识对区域硼矿勘查工作和变质地体的沉积环境分析有借鉴意义。  相似文献   

4.
Boron isotope ratios (11B/10B) have been measured on 60 tourmaline separates from over 40 massive sulfide deposits and tourmalinites from a variety of geologic and tectonic settings. The coverage of these localities is global (5 continents) and includes the giant ore bodies at Kidd Creek and Sullivan (Canada), Broken Hill (Australia), and Ducktown (USA). Overall, the tourmalines display a wide range in 11B values from –22.8 to +18.3 Possible controls over the boron isotopic composition of the tourmalines include: 1) composition of the boron source, 2) regional metamorphism, 3) water/rock ratios, 4) seawater entrainment, 5) temperature of formation, and 6) secular variations in seawater 11B. The most significant control appears to be the composition of the boron source, particularly the nature of footwall lithologies; variations in water/ rock ratios and seawater entrainment are of secondary importance. The boron isotope values seem especially sensitive to the presence of evaporites (marine and non-marine) and carbonates in source rocks to the massive sulfide deposits and tourmalinites.  相似文献   

5.
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   

6.
Tourmalinite from northern Guangxi,China   总被引：1，自引：0，他引：1  
The extensive development of tourmalinite is a feature that distinguishes the northern Guangxi polymetallic tin province of China from similar metallogenic provinces elsewhere. Two types of tourmalinite occur in the province. The first type, in the lower part of the Early Proterozoic Sibao Group, is bedded, stratiform or lenticular tourmalinite that shows well-developed laminated, gel, and degelatinized structures. Its mineral assemblage is very simple and the grain size ranges from 2 to 8 m. This tourmaline is relatively rich in Mg, with an Fe/(Fe + Mg) ratio of 0.25–0.50.The second type of tourmalinite occurs as lodes distributed in the exocontact zone of Late Proterozoic biotite-granite intrusions. Its mineral assemblage is relatively complex; the tourmaline is present as euhedral or subhedral crystals ranging from 0.1 to 3.5 mm, mostly from 0.5 to 1 mm. This tourmaline commonly exhibits a radiating, zoned structure with Fe/(Fe + Mg) ratios of 0.64–0.79. It is suggested that the bedded tourmalinite formed by exhalation in an Early Proterozoic spreading-ridge environment, whereas the vein tourmalinite formed in a plate-convergence setting genetically associated with emplacement of Late Proterozoic biotite granite. As the tourmalinites themselves are related to mineralized rocks and orebodies, their origin and the related boron cycle of the region reflect to some extent the formation and evolution of the associated polymetallic tin deposits of the region.  相似文献   

7.
Integrated studies of seven Proterozoic sediment-hosted, Pb-Zn-Ag sulfide deposits of Brazil, permit the estimation of the age of the hosting sequence and the mineralization, the nature of the sulfur and metal sources, the temperature range of sulfide formation and the environment of deposition. These deposits can be classified into three groups, according to their ages. (a) Archean to Paleoproterozoic: the Boquira deposit, in Bahia state, consists of stratiform massive and disseminated sulfides hosted by parametamorphic sequences of grunnerite-cummingtonite+magnetite that represent a silicate facies of the Boquira Formation (BF). Lead isotope data of galena samples indicate a time span between 2.7 and 2.5 Ga for ore formation, in agreement with the stratigraphic position of the BF. The relatively heavy sulfur isotope compositions for the disseminated and stratiform sulfides (+8.3 to +12.8 ‰ CDT)suggest a sedimentary source for the sulfur. (b) Paleo to Mesoproterozoic: stratiform and stratabound sulfides in association with growth faults are present in the Canoas mine (Ribeira, in Paraná state) and in the Caboclo mineralization (Bahia state). They are hosted by calcsilicates and amphibolites in the Canoas deposit, whereas in the Caboclo area the mineralization is associated with hydrothermally altered dolarenites at the base of the 1.2 Ga Caboclo Formation. The interpreted Pb-Pb age of the Canoas mineralization is coeval with the 1.7 Ga host rocks. Sulfur isotopic data for Canoas sulfides (+1.2 to +16 ‰ CDT) suggest a sea water source for the sulfur. The range between −21.1 and +8.8 ‰ CDT for the Caboclo sulfides could suggest the action of bacterial reduction of seawater sulfates, but this interpretation is not conclusive. (c) Neoproterozoic: stratiform and stratabound sulfide deposits formed during the complex diagenetic history of the host carbonate rocks from the Morro Agudo (Bambui Group), Irecê and Nova Redenção (Una Group), yield heavy sulfur isotope values (+18.9 to +39.4 ‰ CDT). The uniform heavy isotope composition of the barites from these deposits (+25.1 to +40.9 ‰) reflect their origin from Neoproterozoic seawater sulfates. The late-stage, and most important, metallic concentrations represent sulfur scavenged from pre-existing sulfides or from direct reduction of evaporitic sulfate minerals. Lead isotope data from the Bambui Group suggest focused fluid circulation from diverse Proterozoic sediment sources, that probably was responsible for metal transport to the site of sulfide precipitation. (d) Late Proterozoic to Early Paleozoic: lead-zinc sulfides (+pyrite and chalcopyrite) of Santa Maria deposits, in Rio Grande do Sul, form the matrix of arkosic sandstones and conglomerates, and are closely associated with regional faults forming graben structures. Intermediate volcanic rocks are intercalated with the basal siliciclastic members. Lead isotope age of the mineralization (0.59 Ga) is coeval with the host rocks. Sulfur isotopic values between −3.6 and +4.1 are compatible with a deep source for the sulfur.Geological, petrographic and isotopic data of the deposits studied suggest that they were formed during periods of extensional tectonics. Growth faults or reactivated basement structures probably were responsible for localized circulation of metal-bearing fluids within the sedimentary sequences. Sulfides were formed by the reduction of sedimentary sulfates in most cases. Linear structures are important controls for sulfide concentration in these Proterozoic basins.  相似文献   

8.
The isotopic composition of Fe was determined in water, Fe-oxides and sulfides from the Tinto and Odiel Basins (South West Spain). As a consequence of sulfide oxidation in mine tailings both rivers are acidic (1.45 < pH < 3.85) and display high concentrations of dissolved Fe (up to 420 mmol l− 1) and sulphates (up to 1190 mmol l− 1).The δ56Fe of pyrite-rich samples from the Rio Tinto and from the Tharsis mine ranged from − 0.56 ± 0.08‰ to + 0.25 ± 0.1‰. δ56Fe values for Fe-oxides precipitates that currently form in the riverbed varied from − 1.98 ± 0.10‰ to 1.57 ± 0.08‰. Comparatively narrower ranges of values (− 0.18 ± 0.08‰ and + 0.21 ± 0.14‰) were observed in their fossil analogues from the Pliocene–Pleistocene and in samples from the Gossan (the oxidized layer that formed through exposure to oxygen of the massive sulfide deposits) (− 0.36 ± 0.12‰ to 0.82 ± 0.07‰). In water, δ56Fe values ranged from − 1.76 ± 0.10‰ to + 0.43 ± 0.05‰.At the source of the Tinto River, fractionation between aqueous Fe(III) and pyrite from the tailings was less than would be expected from a simple pyrite oxidation process. Similarly, the isotopic composition of Gossan oxides and that of pyrite was different from what would be expected from pyrite oxidation. In rivers, the precipitation of Fe-oxides (mainly jarosite and schwertmannite and lesser amounts of goethite) from water containing mainly (more than 99%) Fe(III) with concentrations up to 372 mmol l− 1 causes variable fractionation between the solid and the aqueous phase (− 0.98‰ < Δ56Fesolid–water < 2.25‰). The significant magnitude of the positive fractionation factor observed in several Fe(III) dominated water may be related to the precipitation of Fe(III) sulphates containing phases.  相似文献   

9.
辽东硼矿床中电气石的矿物学特征及成因意义   总被引：7，自引：0，他引：7  
辽东硼矿床产于早元古代的一套变质岩内，硼矿体赋存于镁质大理岩中。电气石就产在含电气石变（浅）粒岩、电英岩及硼矿体中。电气石的矿物学研究表明：电气石中有Ｍｇ－Ｆｅ和Ｎａ－Ｃａ两个系列；电气石以富镁和钙为特征，ＦｅＯ／（ＦｅＯ＋ＭｇＯ）和Ｎａ２Ｏ／（Ｎａ２Ｏ＋ＣａＯ）比值均小于０．５。不同岩石中的电气石，其矿物学特征明显不同，这些差异反映了它们形成环境的不同，这对成岩成矿有重要的指示意义。经成因分析，电气石是由角闪岩相区域变质作用形成的  相似文献   

10.
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   

11.
Summary In the Archaean Malene supracrustal rocks of West Greenland different types of stratiform tourmalinites have been found. The present article describes schistose anthophyllite-rich tourmalinites hosted in anthophyllite-cordierite schists. It is shown that the boron is of submarine exhalative origin and was absorbed from seaweater by clay minerals. Tourmaline was formed at an early stage of metamorphism up to staurolite grade. At higher metamorphic grades staurolite became unstable and porphyroblasts of cordierite and tourmaline were formed. The boron is suggested to be from the same brines which supplied tungsten for the extensive stratabound scheelite occurrences found in banded amphibolites and in some tourmalinites in the Malene supracrustal belt.
Stratiforme Turmalinite in der archaischen Wolfram-Provinz von West-Grönland
Zusammenfassung In den archaischen suprakrustalen Gesteinen Westgrönlands kommen verschiedene schichtgebundene Turmalinite vor. Schiefrige anthophyllitreiche Turmalinite, die in Anthophyllit-Cordierit-Schiefern auftreten, sind der Gegenstand dieser Untersuchung. Das Bor stammt aus submarinen Exhalationen und wurde an Tonmineralen absorbiert. Turmalin wurde bereits in einem frühen Stadium der Metamorphose bis hin zur Staurolith-Fazies gebildet. Mit steigender Metamorphose bildeten sich Cordierit- und Turmalin-Porphyroblasten auf Kosten von Staurolith. Es wird angenommen, daß das Wolfram in den weitverbreiteten schichtgebundenen Scheelitvorkommen der suprakrustalen Gesteine des Malene-Gürtels ebenso wie das Bor aus submarinen Exhalationen stammt.
  相似文献   

12.
The Houxianyu borate deposit in northeastern China is one of the largest boron sources of China, hosted mainly in the Paleoproterozoic meta-volcanic and sedimentary rocks (known as the Liaohe Group) that are characterized by high boron concentrations. The borate ore-body has intimate spatial relationship with the Mg-rich carbonates/silicates of the Group, with fine-grained gneisses (meta-felsic volcanic rocks) as main country rocks. The presence of abundant tourmalinites and tourmaline-rich quartz veins in the borate orebody provides an opportunity to study the origin of boron, the nature of ore-forming fluids, and possible mineralization mechanism. We report the chemical and boron isotopic compositions of tourmalines from the tourmaline-rich rocks in the borate deposit and from the tourmaline-bearing fine-grained gneisses.Tourmalines from the fine-grained gneisses are chemically homogeneous, showing relatively high Fe and Na and low Mg, with δ11B values in a narrow range from +1.22‰ to +2.63‰. Tourmalines from the tourmaline-rich rocks, however, commonly show compositional zoning, with an irregular detrital core and a euhedral overgrowth, and have significantly higher Mg, REE (and more pronounced positive Eu anomalies), V (229–1852 ppm) and Sr (208–1191 ppm) than those from the fine-grained gneisses. They show varied B isotope values ranging from +4.51‰ to +12.43‰, which plot intermediate between those of the terrigenous sediments and arc rocks with low boron isotope values (as represented by the δ11B = +1.22‰ to +2.63‰ of the fine-grained gneisses of this study) and those of marine carbonates and evaporates with high boron isotope values. In addition, the rim of the zoned tourmaline shows notably higher Mg, Ti, V, Sn, and Pb, and REE (particularly LREEs), but lower Fe, Co, Cr, Ni, Zn, Mn, and lower δ11B values than the core. These data suggest that (1) the sources of boron of the borate ore-body are mainly the Paleoproterozoic meta-volcanic and sedimentary rocks, and (2) the ore-forming fluids should be the high temperature metamorphic fluids related to the amphibolite-facies metamorphism of the Paleoproterozoic foldbelt, which leach boron from the boron-rich meta-volcanic and sedimentary rocks of the Liaohe Group, and the boron-rich metamorphic fluids subsequently interacted with the marine Mg-rich carbonates and evaporates, forming borate deposit, the tourmaline overgrowth in the rim and the tourmaline-rich rocks.  相似文献   

13.
We have measured the boron concentration and isotope composition of regionally expansive borate deposits and geothermal fluids from the Cenozoic geothermal system of the Argentine Puna Plateau in the central Andes. The borate minerals borax, colemanite, hydroboracite, inderite, inyoite, kernite, teruggite, tincalconite, and ulexite span a wide range of δ11B values from −29.5 to −0.3‰, whereas fluids cover a range from −18.3 to 0.7‰. The data from recent coexisting borate minerals and fluids allow for the calculation of the isotope composition of the ancient mineralizing fluids and thus for the constraint of the isotope composition of the source rocks sampled by the fluids. The boron isotope composition of ancient mineralizing fluids appears uniform throughout the section of precipitates at a given locality and similar to values obtained from recent thermal fluids. These findings support models that suggest uniform and stable climatic, magmatic, and tectonic conditions during the past 8 million years in this part of the central Andes. Boron in fluids is derived from different sources, depending on the drainage system and local country rocks. One significant boron source is the Paleozoic basement, which has a whole-rock isotopic composition of δ11B=−8.9±2.2‰ (1 SD); another important boron contribution comes from Neogene-Pleistocene ignimbrites (δ11B=−3.8±2.8‰, 1 SD). Cenozoic andesites and Mesozoic limestones (δ11B≤+8‰) provide a potential third boron source.  相似文献   

14.
Three types of tourmaline occurrence have been identified in the area of Bin Yauri, Nigeria, mesothermal lode-gold mineralization. These are: (1) stratabound tourmalinites in pelitic metasediments, (2) tourmaline in a hydrothermal alteration assemblage within hornfelsed wall rocks, (3) tourmaline in auriferous quartz and quartz-carbonate veins. Although the tourmaline occurrences are all within or close to the contact aureole of a granodiorite intrusion, geochemical characteristics of the tourmalines are broadly similar and reflect a common metasedimentary source. Two stages of tourmalinization are envisaged. The earlier (ca. 1100 Ma) involved syngenetic-diagenetic formation of tourmalinites, while the later (ca. 500 Ma) involved epigenetic (hydrothermal) tourmaline-gold mineralization, possibly derived by dehydration and devolatilization of metasedimentary sequences containing tourmaline-rich rocks or tourmalinites. Electron microprobe analyses indicate that the tourmalines are intermediate members of the schorl-dravite solid solution series. Plots involving FeO, MgO, and/or Al2O3 from these analyses are used to constrain the sources and processes of tourmalinization. Two metallogenic implications are derived from this study. One is that, although the tourmalinites are barren of gold and base metal mineralization, their occurrences nevertheless encourages exploration for syngenetic-exhalative massive sulphide deposits in the region. The other implication applies to the potential use of tourmaline in deciphering the physico-chemical conditions of gold-mineralizing fluids in the Bin Yauri area.  相似文献   

15.
Summary This contribution demonstrates, for the first time, the close genetic relationship of concordant tourmaline rocks (tourmalinites) to stratabound tungsten mineralization and their wide regional distribution within the polymetamorphic Austroalpine Crystalline Complex of the Eastern Alps. The occurrences investigated are located in parts of the Austroalpine Crystalline Complex consisting of metavolcanoclastic and metacalcareous sequences of probable Lower Paleozoic age. Tourmalinites composed of tourmaline, quartz, plagioclase, ± almandine-rich garnet, ± muscovite, ± biotite, and minor ilmenite, rutile, graphite,- ± pyrite and, rarely, scheelite are of pre- to synmetamorphic origin. Tourmalines from the tourmalinites have been identified as intermediate members of the dravite-schorl solid solution series with minor amounts of other tourmaline end members. They can be compared to tourmalines from massive sulphide and stratabound tungsten deposits. Tourmalines from pegmatoids, on the contrary, plot close to the schorl end member. Tourmalinites are interpreted as metamorphosed products of elastic sedimentary material which has reacted with boronrich solutions of probable exhalative-hydrothermal origin. These exhalative processes are genetically connected to the transport of B and W and to the formation of syngenetic/syndiagenetic tungsten mineralization. Metamorphic mobilization of these primary concentrations led, during the Variscan and the Alpine metamorphic events, to the formation of scheelite-bearing quartz-tourmaline-, quartz-plagioclase-tourmaline mobilizates and pegmatoids.
Turmalingesteine und schichtgebundene Scheelitvererzungen im polymetamorphen Kristallin der Ostalpen, österreich
Zusammenfassung Erstmals konnte auch in den Ostalpen die enge genetische Beziehung und weite Verbreitung schichtiger Turmalingesteine (Turmalinite) zu schichtgebundenen Wolframvererzungen gezeigt werden. Die bearbeiteten Vorkommen liegen in Teilen des polymetamorphen ostalpinen Kristallins, eingeschaltet in eine bunte metavulkanoklastisch-, metakarbonatisehe Abfolge, wahrscheinlich altpaläozoischen Alters. Turmalinite setzen sich mineralogisch aus Turmalin, Quarz, Plagioklas, t almandinreichem Granat, ±Muskowit, ± Biotit, untergeordnet Ilmenit, Rutil, Graphit, ± Pyrit und selten Scheelit zusammen und sind prä- bis synmetamorph gebildet worden. Die Turmaline aus den Turmaliniten sind als intermediäre Glieder der Dravit-Schörl-Mischkristallreihe mit untergeordneter Beteiligung anderer Turmalinendglieder bestimmt worden, sie sind in ihrem Mineralchemismus vergleichbar mit Turmalinen aus massiven Sulfid-, und schichtgebundenen Wolframlagerstätten. Turmalin aus Pegmatoiden steht hingegen dem Schörlendglied nahe. Die Turmalinite werden als metamorphe Produkte klastischer Sedimente, die mit borreichen Lösungen, wahrscheinlich exhalativ-hydrothermaler Herkunft, reagiert haben, gedeutet. Diese exhalativen Prozesse stehen mit der Zufuhr von Bor und Wolfram und der Bildung syngenetischer/syndiagenetischer Wolframverer zungen in enger Verbindung. Im Zuge der variszischen und alpinen Orogenesen wurdendiese Ausgangsgesteine mehreren Metamorphosen unterworfen, während der es zur Bildung von scheelitführenden Quarz-Turmalin-, Quarz-Plagioklas-Turmalin-Mobilisaten und Pegmatoiden kam.

With 6 Figures  相似文献   

16.
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   

17.
Chemical composition, unit cell parameters, and trace elements of tourmalines from Mesozoic gold-quartz-sulphide and gold-bearing copper-porphyry ore-magmatic systems of the Trans-Baikal area and Mongolia show that they belong to the specific schorl-dravite highly ferruginous oxytourmaline series. They are low in alumina (Al2O3 = 16–33%) and have MgO contents (up to 10%) and Fe2O3 (1%). There is a direct correlation of unit cell parameters (a,c,V) with total iron, which permits composition estimates from X-ray diffraction analyses. As a rule, these tourmalines contain high concentrations of Au, Pb and Cu, which are mainly hosted by inclusions of native gold and ore minerals. The highest As abundances are contained in the tourmalines of the copper-porphyry field.Two trends of isomorphic replacement are related to increasing Fe content of oxyferruginous tourmalines:(1) “Acid leaching” trend (less ferruginous part of the series) Mg + Fe2+ + 4Al + 40 4Fe3+ + 2 + 4(OH,F); and (2) “conjugate deposition” trend Mg + 1.5Fe2+ + 1.5Al + 4(OH,F) 4Fe3+ + 4O.These features distinguish tourmalines from gold-bearing systems from schorl-dravites of tin and rare-metal deposits. They may be used in metallogenic analyses, interpretation of the origin of primary and secondary anomalies, and assessment of the type and zonation of ore fields.  相似文献   

18.
高任  谢桂青  冯道水  纪云昊  钟浩  张磊 《矿床地质》2023,42(6):1139-1158
钨和铜有明显不同的地球化学性质,但钨、铜在矿床中可以共伴生,原因还不清楚。长江中下游成矿带发育典型的斑岩-矽卡岩-层状铜（钨）多金属成矿系统,其中层状铜（钨）矿体成矿时代数据相对较少。作者以该带九瑞矿集区武山铜矿区新发现的钨矿（化）体为研究对象,开展了矿相学、白钨矿原位U-Pb年代学和元素地球化学的研究。研究发现,武山矿床具有层状、矽卡岩型、斑岩型3类铜矿体均有白钨矿矿化,矿床整体由浅至深存在Cu→Cu-W的分带规律。3类矿石中的白钨矿产状类似,充填在粗粒黄铁矿晶体间隙,或呈浸染状分布,被黄铜矿、闪锌矿等交代,产于退化蚀变阶段;其中斑岩中还存在少量晚世代白钨矿,与石英、黄铁矿共生,形成细脉并穿切花岗闪长斑岩,为石英-硫化物阶段产物。通过对退化蚀变阶段白钨矿进行测年和地球化学研究,作者获得了层状矿体含钨黄铜矿矿石中的白钨矿原位LA-ICP-MS U-Pb同位素年龄为（140.6±1.5）Ma,代表层状铜钨矿体成矿时代,在误差范围内与前人获得的斑岩、矽卡岩型矿体的成矿时代基本一致。层状矿体中白钨矿的稀土元素特征和Sr/Mo值符合岩浆热液矿床特征,相比矽卡岩型、花岗岩型白钨矿,层状矿体中白钨矿具有明显较低Mo含量,反映了形成于相对低氧逸度条件;另外,层状矿体中白钨矿具有正Eu异常和与围岩相近的高Y/Ho值的特征,推测其是流体充分交代了含碳围岩地层导致流体性质的明显改变,并且有利于白钨矿和黄铁矿的沉淀,可从深部黄龙组层间部位形成钨品位更富的黄铁矿矿石得到佐证。文章从白钨矿角度证实层状矿体是斑岩-矽卡岩成矿系统的重要组成部分,提出在九瑞矿集区已知铜矿床的深部,尤其是燕山期中酸性侵入岩与含碳质碳酸盐岩的接触带及黄龙组层位,是寻找富钨矿体的新找矿方向。白钨矿的U-Pb同位素定年为长江中下游成矿带层状矿体的成矿时代提供了新的可靠依据。  相似文献   

19.
The lower valley of Changjiang, from Wuhan of the Hubei Province in the west to Zhenjiang of the Jiangsu Province in the east, contains more than 200 polymetallic (Cu–Fe–Au, Mo, Zn, Pb, Ag) deposits and is one of the most important metallogenic belts in China. This metallogenic belt, situated at the northern margin of the Yangzi craton and bordered by the Dabieshan ultrahigh pressure metamorphic belt to the north, consists mainly of Cambrian–Triassic marine clastic sedimentary rocks and carbonate and evaporite rocks, which overlay a Precambrian basement and are intruded by Yanshanian (205 to 64 Ma) granitoid intrusions and subvolcanic complexes. Repeated tectonism from Late Proterozoic to Triassic resulted in extensively developed networks of faults and folds involving the Cambrian–Triassic sedimentary strata and the Precambrian basement. The Yanshanian granitoid intrusions and subvolcanic complexes in the Lower Changjiang metallogenic belt are characterized by whole-rock δ18O of +8‰ to +10‰, initial 87Sr/86Sr of 0.704 to 0.708, and εNdt from −10 to −17 and have been interpreted to have originated from mixing between juvenile mantle and old crustal materials. Also, the Yanshanian granitoids exhibit eastward younging and increase in alkalinity (i.e., from older calc–alkaline in the west to younger subalkaline–alkaline in the east), which are related to oblique collision between the Yangzi and Sino-Korean cratons and tectonic evolution from early compressional to late extensional or rifting regimes. Most polymetallic deposits in the Lower Changjiang metallogenic belt are clustered in seven districts where the Yanshanian magmatism is particularly extensive: from west to east, Edong, Jiurui, Anqing–Guichi, Luzhong, Tongling, Ningwu and Ningzhen. Mineralization is characterized by the occurrence of three distinct types of orebodies in individual deposits: orebodies in Yanshanian granitoid intrusions, skarn orebodies at the contact zones between the Yanshanian intrusions and Late Paleozoic–Early Mesozoic sedimentary rocks, and stratabound massive sulfide orebodies in the Late Paleozoic–Early Mesozoic sedimentary strata. The most important host sedimentary strata are the Middle Carboniferous Huanglong Formation, Lower Permian and Lower–Middle Triassic carbonate and evaporite rocks. The intrusion-hosted and skarn orebodies exhibit well-developed zonation in alteration assemblages, metal contents, and isotopic compositions within individual deposits, and apparently formed from hydrothermal activities related to the Yanshanian magmatism. The stratabound massive sulfide orebodies in the Late Paleozoic–Early Mesozoic sedimentary strata have long been suggested to have formed from sedimentary or volcano-sedimentary exhalative processes in shallow marine environments. However, extensive research over the last 40 years failed to produce unequivocal evidence for syngenetic mineralization. On the basis of geological relationships and isotope geochemical characteristics, we propose a carbonate-hosted replacement deposit model for the genesis of these stratabound massive sulfide orebodies and associated skarn orebodies. This model suggests that epigenetic mineralization resulted from interactions between magmatic fluids evolved from the Yanshanian intrusions with carbonate and evaporite wall rocks. Mineralization was an integral but distal part of the larger hydrothermal systems that formed the proximal skarn orebodies at the contact zones and the intrusion-hosted orebodies. The stratabound massive sulfide deposits of the Lower Changjiang metallogenic belt share many features with the well-studied, high-temperature, carbonate-hosted replacement deposits of northern Mexico and western United States, particularly with respect to association with small, shallow granitoid complexes, structural and stratigraphic controls on mineralization, alteration assemblages, geometry of orebodies, metal association, metal zonation and isotopic systematics.  相似文献   

20.
Cl-37 in the Dead Sea system---preliminary results   总被引：1，自引：0，他引：1  
This study presents the first set of δ measurements in the Dead Sea environment. δ values for the meromictic (long term stratified) Dead Sea water column prior to its complete overturn in 1979 were −0.47‰ SMOC for the UWM (Upper Water Mass) and +0.55‰ SMOC for the LWM (Lower Water Mass). The δ values for the pre-overturn Dead Sea cannot be explained by the prevailing model on the evolution of the Dead Sea during the last few centuries and require corroboration by more measurements. The 1979 overturn wiped out almost completely the isotopic differences between the UWM and LWM. Even so, Cl isotope data could be used to decipher physical processes related to the overturn such as incomplete homogenization of the deep water mass. Inputs into the lake, comprising freshwaters (springs and the Jordan River) and saline springs gave a range of −0.37‰ to +1.0‰ with the freshwater sources being more enriched in δ . Based on the δ measurements of the End-Brine (the effluent from Dead Sea evaporation ponds) and of recent Dead Sea halite, the Cl isotopic composition of the originating brines have been estimated. They gave a narrow isotopic spread, +0.01‰ and +0.07‰ and fall within the same range with Dead Sea pore water (+0.13‰) and with the post-overturn Dead Sea (−0.03‰ and +0.16‰). Rock salt from Mount Sdom gave a value of −0.59‰ indicating its formation at the last stages of halite deposition from evaporating sea water. The hypersaline En Ashlag spring gave a depleted δ value of −0.32‰, corresponding to a residual brine formed in the very latest stages (including bishofite deposition) of seawater evaporation.  相似文献   

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