Mineral chemistry and chemical zoning in tourmalines, Pampa del Tamboreo, San Luis, Argentina

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.     

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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⁺/Fe_tot,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 x_Mg（mole fraction of Mg） close to that of the hrst stage tourmaline,due to a close association with pyrite and arsenopyrite.From Fe³⁺/Fe_tot 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.     

Stable isotope compositions of tourmalines from granites and related hydrothermal rocks of the Karagwe-Ankolean belt,northwest Tanzania

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 Fe_tot/(Fe_tot + Mg ratio)] and isotopic composition that relate to evolving magmatic and hydrothermal conditions. Igneous differentiation [increasing Fe_tot/(Fe_tot + Mg) in magmatic tourmaline] has produced trends with higher δ¹⁸O in quartz, lower δ¹⁸O in tourmaline, and larger Δ_QTZ.−TOUR.-values, that reflect a combination of a reduction of crystallization temperature and an increase of Fe_tot/ (Fe_tot + 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 Fe_tot/(Fe_tot + Mg) ratios, and progressively lower δ¹⁸O and δD -values.     

Tourmalinites from the Eastern Sierras Pampeanas, Argentina

In the eastern Sierras Pampeanas, Central Argentina, tourmalinites and coticules are found in close association with stratabound scheelite deposits in metamorphic terranes. In Sierra Grande (Agua de Ramón and Ambul districts) and Sierra de Altautina, tourmalinites are associated with stratabound scheelite deposits related to orthoamphibolites. In the Pampa del Tamboreo area, tourmalinites are located in biotite schists stratigraphically related to acid to intermediate metavolcanic rocks and scheelite-bearing quartzites.The mineral chemistry and boron isotopic compositions of tourmalinite-hosted and vein-hosted tourmalines are investigated. Overall, the tourmalines belong to the dravite-schorl series and are generally aluminous; Fe/(Fe+Mg) ranges from 0.33 to 0.85, Al/(Al+Fe+Mg) from 0.66 to 0.76 and the amount of X-site vacancy (0.12–0.48) indicates significant foitite components. Their boron isotopic compositions (δ¹¹B) are from −24.0‰ to−15.0‰.Similar mineral chemistries and boron isotopic values for tourmaline in tourmalinites related to stratabound scheelite mineralisation and in tungsten-bearing quartz veins suggest a common source for the boron and probably the tungsten. The field, chemical and isotopic relationships are consistent with tungsten and boron in quartz-vein deposits being remobilised from stratabound scheelite and tourmalinite, dominantly by liquid-state transfer associated with regional shear zones. Tungsten and boron in the original sedimentary sequence (now meta-exhalites) are ascribed to volcanogenic exhalations.     

Protomylonite evolution potentially revealed by the 3D depiction and fractal analysis of chemical data from a feldspar

Tourmalinization associated with peraluminous granitic intrusions in metapelitic host-rocks has been widely recorded in the Iberian Peninsula, given the importance of tourmaline as a tracer of granite magma evolution and potential indicator of Sn-W mineralizations. In the Penamacor-Monsanto granite pluton (Central Eastern Portugal, Central Iberian Zone), tourmaline occurs: (1) as accessory phase in two-mica granitic rocks, muscovite-granites and aplites, (2) in quartz (±mica)-tourmaline rocks (tourmalinites) in several exocontact locations, and (3) as a rare detrital phase in contact zone hornfels and metapelitic host-rocks. Electron microprobe and stable isotope (δ¹⁸O, δD, δ¹¹B) data provide clear distinctions between tourmaline populations from these different settings: (a) schorl–oxyschorl tourmalines from granitic rocks have variable foititic component (^X□ = 17–57 %) and Mg/(Mg + Fe) ratios (0.19–0.50 in two-mica granitic rocks, and 0.05–0.19 in the more differentiated muscovite-granite and aplites); granitic tourmalines have constant δ¹⁸O values (12.1 ± 0.1 ‰), with wider-ranging δD (?78.2 ± 4.7 ‰) and δ¹¹B (?10.7 to ?9.0 ‰) values; (b) vein/breccia oxyschorl [Mg/(Mg + Fe) = 0.31–0.44] results from late, B- and Fe-enriched magma-derived fluids and is characterized by δ¹⁸O = 12.4 ‰, δD = ?29.5 ‰, and δ¹¹B = ?9.3 ‰, while replacement tourmalines have more dravitic compositions [Mg/(Mg + Fe) = 0.26–0.64], close to that of detrital tourmaline in the surrounding metapelitic rocks, and yield relatively constant δ¹⁸O values (13.1–13.3 ‰), though wider-ranging δD (?58.5 to ?36.5 ‰) and δ¹¹B (?10.2 to ?8.8 ‰) values; and (c) detrital tourmaline in contact rocks and regional host metasediments is mainly dravite [Mg/(Mg + Fe) = 0.35–0.78] and oxydravite [Mg/(Mg + Fe) = 0.51–0.58], respectively. Boron contents of the granitic rocks are low (<650 ppm) compared to the minimum B contents normally required for tourmaline saturation in granitic melts, implying loss of B and other volatiles to the surrounding host-rocks during the late-magmatic stages. This process was responsible for tourmalinization at the exocontact of the Penamacor-Monsanto pluton, either as direct tourmaline precipitation in cavities and fractures crossing the pluton margin (vein/breccia tourmalinites), or as replacement of mafic minerals (chlorite or biotite) in the host-rocks (replacement tourmalinites) along the exocontact of the granite. Thermometry based on ¹⁸O equilibrium fractionation between tourmaline and fluid indicates that a late, B-enriched magmatic aqueous fluid (av. δ¹⁸O ~12.1 ‰, at ~600 °C) precipitated the vein/breccia tourmaline (δ¹⁸O ~12.4 ‰) at ~500–550 °C, and later interacted with the cooler surrounding host-rocks to produce tourmaline at lower temperatures (400–450 °C), and an average δ¹⁸O ~13.2 ‰, closer to the values for the host-rock. Although B-metasomatism associated with some granitic plutons in the Iberian Peninsula seems to be relatively confined in space, extending integrated studies such as this to a larger number of granitic plutons may afford us a better understanding of Variscan magmatism and related mineralizations.     

Tourmaline from the Archean G.R.Halli gold deposit,Chitradurga greenstone belt,Dharwar craton （India）： Implications for the gold metallogeny

Tourmaline occurs as a minor but important mineral in the alteration zc,ne of the Archean orogenic gold deposit of Guddadarangavanahalli （G.R.Halli） in the Chitradurga greenst~ne belt of the western Dharwar craton, southern India. It occurs in the distal alteration halo of the G.R.Halli golcl deposit as （a） clusters of very fine grained aggregates which form a minor constituent in the natrix of the altered metabasalt （AMB tourmaline） and （b） in quartz-carbonate veins （vein tourmaline）. ~[＇he vein tourmaline, based upon the association of specific carbonate minerals, is further grouped as （i） albite-tourmaline-ankerite-quartz veins （vein-1 tourmaline） and （ii） albite-tourmaline-calcite-quartz veins （vein-2 tourmaline）. Both the AMB tourmaline and the vein tourmalines （vein-I and vein-2） belong to the alkali group and are clas- sified under schorl-dravite series. Tourmalines occurring in the veins are zoned while the AMB tour- malines are unzoned. Mineral chemistry and discrimination diagrams 1eveal that cores and rims of the vein tourmalines are distinctly different. Core composition of the ve：n tourmalines is similar to the composition of the AMB tourmaline. The formation of the AMB tourmaline and cores of the vein tour- malines are proposed to be related to the regional D1 deformational event associated with the emplacement of the adjoining ca. 2.61 Ga Chitradurga granite whilst rims of the vein tourmalines vis-a- vis gold mineralization is spatially linked to the juvenile magmatic accretion （2.56-2.50 Ga） east of the studied area in the western part of the eastern Dharwar craton.     

Elemental and boron isotopic variations in tourmaline in two-mica granite from the Cuona area,Tibet: Insights into the evolution of leucogranitic melt

Two-mica granite is the most common magmatic rock type in the Himalayan leucogranite belt, which has close relationship with rare metal mineralization. Its genesis is generally attributed to magmatic differentiation. In recent years, the mineral geochemical compositions are increasingly used to study magmatic differentiation, which are significant for deciphering the melt evolution and element migration processes. In this study, in-situ major and trace element and boron isotope compositions for tourmalines from two-mica granites in the Cuona and Cuonadong leucogranites in the Cuona area are conducted to determine microscopic changes in mineral assemblages and geochemical compositions. Analytical results show that the tourmalines in the Cuonadong leucogranite were crystallized earlier relative to the tourmalines in the Cuona leucogranite during magmatic differentiation. The volatile contents have a genetic relationship with incompatible elements in tourmaline, which is possibly responsible for the formation of tourmaline zonation and the enrichment of Sr, Zn, and Pb during magmatic differentiation. The B isotopic composition of tourmaline in the Cuona area suggests that the granitic magma was dominantly derived from the partial melting of the metasedimentary source rocks. Their B isotope variations likely resulted from fluid exsolution during B-rich melt evolution. High rare metal contents in tourmalines indicate that the two-mica granites in the Cuona area may have great mineralization potential.     

Trace-element and Sr–Nd isotopic evidence for the origin of the Sardinian fluorite mineralization (Italy)

The fluorite-bearing hydrothermal mineralization in Sardinia mainly occurs within Paleozoic volcanic and metasedimentary rocks. Only 3 occurrences are located in volcanic and siliciclastic Cenozoic rocks. Most Sardinian fluorites exhibit relatively high rare earth and Y (REY) contents, strong positive Y anomalies, slightly negative Ce and generally positive Eu anomalies. These features indicate that the REY were mobilized mainly from non-carbonate rocks. Neither Sr nor Nd isotopes can be used to date radiometrically the Sardinian fluorites. However, the measured Sr-isotope ratios of the fluorites hosted by Paleozoic rocks fit mixing lines in the 1000/Sr versus ⁸⁷Sr/⁸⁶Sr plot once recalculated at 280 Ma, suggesting that the age inferred for the correction probably represents that of the formation of the fluorite mineralization. Mixing likely occurred between diluted surficial waters and brines circulating mainly through the Lower Paleozoic metasedimentary basement. The Cenozoic fluorites exhibit chemical and isotopic features similar to those of the Paleozoic fluorites, except the Nuraghe Onigu fluorite displaying a possible contribution of Sr from Cenozoic magmatic rocks. The initial ε_Nd values of the Paleozoic fluorites fit the age proposed for the formation of the deposits. Moreover, the values suggest that radiogenic Nd was provided to the fluids from the Ordovician siliciclastic basement, except for 3 deposits where the potential source rocks of Nd were mainly Ordovician acidic magmatic rocks. The initial ε_Nd values of the Cenozoic fluorites suggest a provenance of Nd essentially from the leaching of Variscan granitoids.     

Duality and genetic significance of REE speciation in tourmaline from tin deposits of the Far East

The distribution of REEs and some minor elements in tourmalines of different associations and deposits of the Russian Far East is studied by the methods of ICP-MS, ICP-MS with laser ablation and scanning electron microscopy. The duality of REE speciation in tourmaline is established: in high-temperature varieties, most REEs (mainly HREEs) are incorporated in rare minerals (monazite, xenotime, zircon, and F–Ce–Y carbonate), whereas hydrothermal ores are characterized by isomorphic incorporation of LREEs in the mineral structure, as well as by a fine admixture of zircon at the expense of detrital clasts in flyschoid rocks with the zones of tourmalinization.     

中条山铜矿区电气石特征及其对成岩成矿作用的示踪意义

中条山地区是我国著名的铜矿床集中区。在胡-篦型层控铜矿床容矿热液沉积岩建造和铜矿峪型铜矿床容矿钙碱性次火山-火山沉积岩系及其它地质环境内发现有大量电气石产出。电气石均属镁-铁系列,且以不含锂为主要特征。电气石由海底盆地热液沉积作用、火山热液喷气作用及热液交代作用形成。这些地质作用的产生均与中条山地区21亿年左右的岩浆活动有关。由于形成条件和形成方式不同,在不同地质环境产出的电气石具有明显不同的光性和标型特征。     

Boron,sulphur and copper isotope systematics in the orogenic gold deposits of the Archaean Hattu schist belt,eastern Finland

The Hattu schist belt is located in the western part of the Archaean Karelian domain of the Fennoscandian Shield. The orogenic gold deposits with Au–Bi–Te geochemical signatures are hosted by NE–SW, N–S and NW–SE oriented shear zones that deform 2.76–2.73 Ga volcanic and sedimentary sequences, as well as 2.75–2.72 Ga tonalite–granodiorite intrusions and diverse felsic porphyry dykes. Mo–W mineralization is also present in some tonalite intrusions, both separate from, and associated with Au mineralization. Somewhat younger, unmineralized leucogranite intrusions (2.70 Ga) also intrude the belt. Lower amphibolite facies peak metamorphism at 3–5 kbar pressures and at 500–600 °C temperatures affected the belt at around 2.70 Ga and post-date hydrothermal alteration and ore formation. In this study, we investigated the potential influence of magmatic-hydrothermal processes on the formation of orogenic gold deposits on the basis of multiple stable isotope (B, S, Cu) studies of tourmaline and sulphide minerals by application of in situ SIMS and LA ICP MS analytical techniques.Crystal chemistry of tourmaline from a Mo–W mineralization hosted by a tonalite intrusion in the Hattu schist belt is characterized by Fe^3 +–Al^3 +-substitution indicating relatively oxidizing conditions of hydrothermal processes. The range of δ¹¹B data for this kind of tourmaline is from − 17.2‰ to − 12.2‰. The hydrothermal tourmaline from felsic porphyry dyke swith gold mineralization has similar crystal chemistry (e.g. dravite–povondraite compositional trend with Fe^3 +–Al^3 + substitution) and δ¹¹B values between − 19.0‰ and − 9.6‰. The uvite–foitite compositional trend and δ¹¹B ‰ values between − 24.1% and − 13.6% characterize metasomatic–hydrothermal tourmaline from the metasediment-hosted gold deposits. Composition of hydrothermal vein-filling and disseminated tourmaline from the gold-bearing shear zones in metavolcanic rocks is transitional between the felsic intrusion and metasedimentary rock hosted hydrothermal tourmaline but the range of average boron isotope data is essentially identical with that of the metasediment-hosted tourmaline. Rock-forming (magmatic) tourmaline from leucogranite has δ¹¹B values between − 14.5‰ and − 10.8‰ and the major element composition is similar to that of the metasediment-hosted tourmaline.The range of δ³⁴S_VCDT values measured in pyrite, chalcopyrite and pyrrhotite is from − 9.1 to + 8.5‰, which falls within the typical range of sulphur isotope data for Archaean orogenic gold deposits. In the Hattu schist belt, positive δ³⁴S_VCDT values characterize metasediment-hosted gold ores with sulphide parageneses dominated by pyrrhotite and arsenopyrite. The δ³⁴S_VCDT values are both positive and negative in ore mineral parageneses within felsic intrusive rocks in which variable amounts of pyrrhotite are associated with pyrite. Purely negative values were only recorded from the pyrite-dominated gold mineralization within metavolcanic units. Therefore the shift of δ³⁴S_VCDT values to the negative values reflects precipitation of sulphide minerals from relatively oxidizing fluids. The range of measured δ⁶⁵Cu_NBS978 values from chalcopyrite is from − 1.11 to 1.19‰. Positive values are common for mineralization in felsic intrusive rocks and negative values are more typical for deposits confined to metasedimentary rocks. Positive and negative δ⁶⁵Cu_NBS978 values occur in the ores hosted by metavolcanic rocks. There is no correlation between sulphur and copper isotope data obtained in the same chalcopyrite grains.Evaluation of sulphur and boron isotope data together and comparisons with other Archaean orogenic gold provinces supports the hypothesis that the metasedimentary rocks were the major sources of sulphur and boron in the orogenic gold deposits in the Hattu schist belt. Variations in major element and boron isotope compositions in tourmaline, as well as in the δ³⁴S_VCDT values in sulphide minerals are attributed to localized involvement of magmatic fluids in the hydrothermal processes. The results of copper isotope studies indicate that local sources of copper in orogenic gold deposits may potentially be recognized if the original, distinct signatures of the sources have not been homogenized by widespread interaction of fluids with a large variety of rocks and provided that local chemical variations have been too small to trigger changes in the oxidation state of copper during hydrothermal processes.     

辽宁古元古代地体中富电气石岩石的成因：蒸发岩硼源的证据

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。     

Tourmaline in Proterozoic Massive Sulfide Deposits from Rajasthan, India

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     

Boron isotopic composition of tourmaline from massive sulfide deposits and tourmalinites

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.     

Mineralogy, geochemistry and geological significance of tourmaline-rich rocks from the Paleozoic Cinco Villas massif (western Pyrenees, Spain)

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     

电气石——成岩成矿作用的灵敏示踪剂

本文详细论述了电气石的化学组成（主化学元素、微量元素和稀土元素）和同位素组成Ｈ、Ｏ、Ｂ、Ｓｉ、Ｒｂ／Ｓｒ、Ｓｍ／Ｎｄ、ｐｂ／ｐｂ和Ｋ／Ａｒ）特征,提出电气石可以作为研究成岩成矿作用的一个灵敏示踪剂。利用电气石的主化学元素和微量、稀土元素组成,可以有效指示其形成的物理化学环境,还可以作为一种有用的找矿标志,指标矿化的存在,并可能用于区分矿化类型和矿体规模。电气石的稳定同位素和放射性同位素研究,已经用     

Boron metasomatism and behaviour of rare earth elements during formation of tourmaline rocks in the eastern Arunta Inlier,central Australia

Tourmaline rocks of previously unclear genesis and spatially associated with W- (Cu)-bearing calc-silicate rocks occur in Palaeoproterozoic supracrustal and felsic intrusive rocks in the Bonya Hills in the eastern Arunta Inlier, central Australia. Tourmalinisation of metapelitic host rocks postdates the peak of regional low-pressure metamorphism (M₁/D₁, ~500 °C, ~0.2 GPa), and occurred synkinematically between the two main deformation events D₁ and D₂, coeval with emplacement of Late Strangways (~1.73 Ga) tourmaline-bearing leucogranites and pegmatites. Tourmaline is classified as schorl to dravite in tourmaline–quartz rocks and surrounding tourmaline-rich alteration zones, and as Fe-rich schorl to foitite in the leucogranites. Boron metasomatism resulted in systematic depletion of K, Li, Rb, Cs, Mn and enrichment of B, and in some samples of Na and Ca, in the tourmaline rocks compared to unaltered metasedimentary host rocks. Whole-rock REE concentrations and patterns of unaltered schist, tourmalinised schist and tourmaline–quartz veins—the latter were the zones of influx of the boron-rich hydrothermal fluid—are comparable to those of post-Archaean shales. Thus, the whole-rock REE patterns of these rocks are mostly controlled by the metapelitic precursor. In contrast, REE concentrations of leucogranitic rocks are low (10 times chondritic), and their flat REE patterns with pronounced negative Eu anomalies are typical for fractionated granitic melts coexisting with a fluid phase. REE patterns for tourmalines separated from metapelite-hosted tourmaline–quartz veins and tourmaline-bearing granites are very different from one another but each tourmaline pattern mirrors the REE distribution of its immediate host rock. Tourmalines occurring in tourmaline–quartz veins within tourmalinised metasediments have LREE-enriched (La_N/Yb_N=6.3–55), shale-like patterns with higher REE (54–108 ppm). In contrast, those formed in evolved leucogranites exhibit flat REE patterns (La_N/Yb_N=1.0–5.6) with pronounced negative Eu anomalies and are lower in REE (5.6–30 ppm). We therefore conclude that REE concentrations and patterns of tourmaline from the different tourmaline rocks studied are controlled by the host rock and not by the hydrothermal fluid causing boron metasomatism. From the similarity of the REE pattern of separated tourmaline with the host rock, we further conclude that incorporation of REEs in tourmaline is not intrinsically controlled (i.e. by crystal chemical factors). Tourmaline does not preferentially fractionate specific REEs or groups of REEs during crystallisation from evolved boron- and fluid-rich granitic melts or during alteration of clastic metasediments by boron-rich magmatic-hydrothermal fluids.Editorial responsibility: J. Hoefs     

Structural and geochronological studies on the Liba goldfield of the West Qinling Orogen, Central China

The Liba goldfield, located to the northeast of the Zhongchuan Granite in the West Qinling Orogen (WQO) of mainland China, contains the largest known gold resource of 2.8 Moz in the Zhongchuan area. Devonian metasedimentary rocks host the structurally controlled gold mineralization, which is associated with silica–sericite–chlorite–carbonate alteration. Two major styles of mineralization occurred at the goldfield, which are disseminated sediment-hosted and quartz vein hosted types. Pyrite, arsenopyrite, and arsenian pyrite are major gold carriers and gold also occurs as native gold grains and electrum spatially associated with the sulfides. Numerous felsic/intermediate dykes have a similar structural control as the mineralization, and their contacts with host rocks are recognized as favorable zones for mineralization. Detailed fieldwork in conjunction with geochronological studies has helped to define the deformation history and gold metallogenesis of the goldfield. Three major phases of deformation have been recognized in the Zhongchuan area. The first deformation (D₁) event was compressional in broadly a N–S orientation, the second (D₂) event was also compressional and orientated in a NE–SW direction, and the third (D₃) event was post-mineralization and was associated with the emplacement of barren calcite and anhydrite veins. Compression related to D₂ is the key process that controlled the distribution of igneous dykes and gold mineralization in the Liba goldfield. Both igneous and hydrothermal fluids preferentially focused along dilational jogs under local trans-extension, which took place during the late stage of D₂. Precise dating with high-resolution ion microprobe (SHRIMP) U–Pb on zircon and ⁴⁰Ar/³⁹Ar on muscovite, biotite, hornblende, and plagioclase of crosscutting pre-mineralization granitic porphyry and diorite dykes have constrained the mineralization age to after ca. 227 Ma. ⁴⁰Ar/³⁹Ar analysis of minerals formed in hydrothermal alteration zones associated with gold mineralization indicates that there was a widespread ca. 216 Ma hydrothermal event that affected almost all lithologies in the area. This detailed investigation is the first study to tightly constrain the timing of gold mineralization in the WQO. The broadly overlapping timing and similar structural control of the mineralization and igneous dykes show a promising correlation, which could be potentially used to map this Late Triassic gold mineralization event in the WQO.     

Geochemistry and petrography of gold-quartz-tourmaline veins of the Okote area, southern Ethiopia: implications for gold exploration

Summary Quartz-tourmaline vein-hosting rocks of the Okote area belong to the Neoproterozoic Adola Belt. Metasomatic auriferous quartz-tourmaline veins occur in ductile N–S trending, sinistral shear zones. These veins commonly contain quartz, carbonates, and tourmaline, with minor pyrite, and accessory chalcopyrite, pyrrhotite, and gold. Tourmaline forms isolated euhedral crystals in the fracture surfaces of quartz carbonate veins. Many of the tourmaline crystals are optically zoned with a bluish core and a bluish to brown rim. Electron microprobe analyses show that the tourmalines comprise an intermediate dravite-schorl solid solution with a mean FeO/(FeO + MgO) = 0.47. Abrupt transitions between the colour zones within single tourmaline crystals are accompanied by relative variations in the FeO/(FeO + MgO) ratios. The tourmaline separates indicate that the tourmalines contain highly variable average contents of trace elements. Chondrite-normalized rare earth element (REE) abundances of tourmaline separates from auriferous veins show LREE-enriched to LREE-depleted patterns with negative to positive Eu anomalies and a flat, near-chondritic HREE pattern. The auriferous quartz-tourmaline veins have LREE-enriched patterns without a Eu anomaly and a flat HREE pattern, but tourmaline-free gold-quartz veins have very low REE contents and LREE-depleted patterns also without Eu anomalies. The FeO/(FeO + MgO) ratios, major and trace element compositions, and the types of wall-rock alteration are used to suggest that the sources of boron are dominantly metamorphic (dehydration and devolatilization processes), but do not totally exclude the possibility of a magmatic source. The occurrences of high-grade gold associated with tourmaline make tourmaline a valuable prospecting guide for hydrothermal gold mineralization in the Adola Belt, southern Ethiopia. Received November 17, 1999; revised version accepted July 23, 2001     

加拿大Sullivan超大型Pb-Zn-Ag矿床中几个指示成矿环境的特征矿物研究

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。