山西省中条山铜矿田电气石与电气石岩的研究

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     

Tourmaline in a low grade clastic metasedimentary rock: an example of the petrogenetic potential of tourmaline

Detrital tourmaline grains and their associated tourmaline overgrowths provide a means to unravel the provenance and petrogenetic history of low grade clastic metasedimentary rocks. Evidence derives from tourmaline grains found in a lithic wacke metamorphosed to chlorite zone conditions. The detrital tourmaline cores are diagnostic indicators of the source rocks of the sediment whereas the overgrowths record both diagenetic and metamorphic reactions in the rock. Tourmaline grains consist of a detrital core surrounded by asymmetric overgrowths comprised of inner and outer rims. Abrupt chemical discontinuities between each of these zones implies that volume diffusion within tourmaline was minor under the conditions of formation. Compositions of the detrital cores vary widely, yet can be correlated with source rock types that are consistent with lithic fragments recognizable in the metawacke. At either the analogous or antilogous pole, inner rim compositions proximal to the detrital cores converge, despite the substrate tourmaline composition, indicating an approach to chemical equilibrium. However, significant dufferences in Al and X-site vacancies at the expense of Mg, Na and Ti between the analogous and antilogous poles of the inner rims demonstrate the presence of significant amounts of compositional polarity. Outer rim compositions at either pole also converge but compositional polarity between the analogous and antilogous poles persists. The presence of the inner and outer rims separated by a compositional discontinuity suggests punctuated evolution of the overgrowth. This implies that boron was sporadically available during diagenesis and metamorphism. Based on boron contents of minerals, this may correspond to a mechanism such as boron release due to polytypic change of illite or consumption of illite and/or muscovite. As such, tourmaline growth stages may serve as a monitor of chemical reactions in low grade metamorphic rocks.     

Hydrothermal gold mineralization at the Hira Buddini gold mine,India: constraints on fluid evolution and fluid sources from boron isotopic compositions of tourmaline

We determined the boron isotope and chemical compositions of tourmaline from the Hira Buddini gold deposit within the Archean Hutti-Maski greenstone belt in southern India to investigate the evolution of the hydrothermal system and to constrain its fluid sources. Tourmaline is a minor but widespread constituent in the inner and distal alteration zones of metabasaltic and metadacite host rocks associated with the hydrothermal gold mineralization. The Hira Buddini tourmaline belongs to the dravite–schorl series with variations in Al, Fe/(Fe+Mg), Ca, Ti, and Cr contents that can be related to their host lithology. The total range of δ¹¹B values determined is extreme, from −13.3‰ to +9.0‰, but 95% of the values are between −4 and +9‰. The boron isotope compositions of metabasalt-hosted tourmaline show a bimodal distribution with peak δ¹¹B values at about −2‰ and +6‰. The wide range and bimodal distribution of boron isotope ratios in tourmaline require an origin from at least two isotopically distinct fluid sources, which entered the hydrothermal system separately and were subsequently mixed. The estimated δ¹¹B values of the hydrothermal fluids, based on the peak tourmaline compositions and a mineralization temperature of 550°C, are around +1 and +10‰. The isotopically lighter of the two fluids is consistent with boron released by metamorphic devolatilization reactions from the greenstone lithologies, whereas the ¹¹B-rich fluid is attributed to degassing of I-type granitic magmas that intruded the greenstone sequence, providing heat and fluids to the hydrothermal system. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

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     

东秦岭花岗伟晶岩中电气石地球化学特征及成矿指示意义

东秦岭地区是我国重要的花岗伟晶岩区及稀有金属成矿区.电气石在东秦岭各类花岗伟晶岩中广泛发育,通常在无矿化伟晶岩、铍矿化及锂矿化伟晶岩中呈黑色-深蓝色.本文旨在通过各类伟晶岩中电气石的对比研究揭示电气石地球化学特征对东秦岭伟晶岩矿化类型的指示作用.本文所研究电气石为作为东秦岭各类伟晶岩贯通矿物的黑电气石系列.在双峰村、碾...     

Boron isotopic variations in tourmaline from metacarbonates and associated calc-silicate rocks from the Bohemian Massif: Constraints on boron recycling in the Variscan orogen

Various metacarbonate and associated calc-silicate rocks form minor but genetically significant components of the lithological units in the Bohemian Massif of the Variscan orogen in Central Europe.These rocks vary in terms of their lithostratigraphy,chemical composition and mineral assemblage(dolomite/calcite ratio,silicate abundance).Tourmaline is present in five paragenetic settings within the metacarbonate and calc-silicate units.TypeⅠcomprises individual,euhedral,prismatic grains and grain aggregates in a carbonate-dominant(calcite±dolomite)matrix poor in silicates.TypeⅡis characterized by euhedral to subhedral grains and coarse-to fine-grained aggregates in silicate-rich layers/nests within metacarbonate bodies whereas typeⅢoccurs as prismatic grains and aggregates at the contact zones between carbonate and associated silicate host rocks.TypeⅣis in veins crosscutting metacarbonate bodies,and typeⅣtourmaline occurs at the exocontacts of elbaite-subtype granitic pegmatite.Tourmaline from the different settings shows distinctive compositional features.Typical for typeⅠare Mg-rich compositions,with fluor-uvite>dravite>>magnesio-lucchesiite.Tourmalines from typeⅡsilicate-rich layers/nests are highly variable,corresponding to oxy-schorl,magnesio-foitite,Al-rich dravite and fluor-uvite.Typical for typeⅢtourmalines are Ca,Ti-bearing oxy-dravite compositions.The typeⅣveins feature dravite and fluor-uvite tourmaline compositions whereas typeⅤtourmaline is Li,F-rich dravite.Tourmaline is the only Bbearing phase in paragenetic typesⅠ-Ⅳ,where it is characterised by two principal ranges of B-isotope composition(δ^11B=-13‰to-9‰and-18‰to-14‰).These ranges correspond to regionally different units of the Moldanubian Zone.Thus,the Svratka Unit(Moldanubian Zone s.l.)contains only isotopically lighter tourmaline(δ^11B=-18‰to-14‰),whereas metacarbonates in the Poli?ka unit(Teplá-Barrandian Zone)and Olesnice unit(Moravicum of the Moravo-Silesian Zone)has exclusively isotopically heavier tourmaline(δ^11B=-9‰to-13‰).Tourmalines from metacarbonates in the Variegated Unit cover both ranges of isotope composition.The isotopically light end of the B isotope range may indicate the presence of continental evaporites within individual investigated areas.On the other hand,variations in the range of~8δ-units is consistent with the reported shift in B isotopic composition of metasedimentary rocks of the Bohemian Massif due to the prograde metamorphism from very-low grade to eclogite facies.In contrast to the metacarbonate-hosted settings,tourmaline of paragenetic type V from the exocontact of granitic pegmatites displays a significantly heavier range ofδ^11B(as low as-7.7‰to-0.6‰),which is attributed to partitioning of 10 B to cogenetic axinite and/or different B-signature of the source pegmatite containing tourmaline with heavyδ^11B signature.     

Provenance of late Palaeozoic metasediments of the Patagonian proto-Pacific margin (southernmost Chile and Argentina)

In this provenance study of late Palaeozoic metasediments of the Eastern Andean Metamorphic Complex (EAMC) along the south Patagonian proto-Pacific margin of Gondwana, the palaeogeological setting of the continental margin in Devonian–Carboniferous and Permian times is reconstructed. The study is based on detrital heavy mineral contents, chemical compositions of tourmaline grains, and whole rock element and Nd-Sr isotopic compositions. Element and isotopic compositions reveal that Devonian–Carboniferous metaturbidites deposited before the development of a Late Carboniferous–Permian magmatic arc along the margin were mainly fed from felsic, recycled, old continental rocks. The last recycling phase involved erosion of metasediments that were exposed in Patagonia. Feeder systems to the basin cut either through epidote-rich or garnet-rich metasediments. In Permian time, EAMC metaturbidites were deposited next to the evolving magmatic arc and were derived from felsic, crustal rocks. Two provenance domains are recognised. The metasediments of the northern one are chemically similar to those of the Devonian–Carboniferous metasediments. This domain was fed from the metasedimentary host rocks of the magmatic arc. The southern domain probably was fed from the arc proper, as indicated mainly by the dominance of metaplutonic lithic fragments, abundant detrital biotite, and the major element composition of the metasediments.     

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.     

Nature and source of the ore-forming fluids associated with orogenic gold deposits in the Dharwar Craton

Neoarchean orogenic gold deposits, associated with the greenstone-granite milieus in the Dharwar Craton include(1) the famous Kolar mine and the world class Hutti deposit;(2) small mines at HiraBuddini, Uti, Ajjanahalli, and Guddadarangavanahalli;(3) prospects at Jonnagiri; and(4) old mining camps in the Gadag and Ramagiri-Penakacherla belts. The existing diametric views on the source of ore fluid for formation of these deposits include fluids exsolved from granitic melts and extracted by metamorphic devolatilization of the greenstone sequences. Lode gold mineralization occurs in structurally controlled higher order splays in variety of host rocks such as mafic/felsic greenstones, banded iron formations, volcaniclastic rocks and granitoids. Estimated metamorphic conditions of the greenstones vary from lower greenschist facies to mid-amphibolite facies and mineralizations in all the camps are associated with distinct hydrothermal alterations. Fluid inclusion microthermometric and Raman spectroscopic studies document low salinity aqueous-gaseous(H_2O + CO_2 ± CH_4 + NaCl) ore fluids,which precipitated gold and altered the host rocks in a narrow P-T window of 0.7-2.5 kbar and 215-320℃. While the calculated fluid O-and C-isotopic values are ambiguous, S-isotopic compositions of pyrite-precipitating fluid show distinct craton-scale uniformity in terms of its reduced nature and a suggested crustal sulfur source.Available ages on greenstone metamorphism, granitoid plutonism and mineralization in the Hutti Belt are tantamount, making a geochronology-based resolution of the existing debate on the metamorphic vs.magmatic fluid source impossible. In contrast, tourmaline geochemistry suggests involvement of single fluid in formation of gold mineralization, primarily derived by metamorphic devolatilization of mafic greenstones and interlayered sedimentary rocks, with minor magmatic contributions. Similarly, compositions of scheelite, pyrite and arsenopyrite point toward operation of fault-valves that caused pressure fluctuation-induced fluid phase separation, which acted as the dominant process of gold precipitation,apart from fluid-rock sulfidation reactions. Therefore, results from geochemistry of hydrothermal minerals and those from fluid inclusion microthermometry corroborate in constraining source of ore fluid,nature of gold transport(by Au-bisulfide complex) and mechanism of gold ore formation in the Dharwar Craton.     

Multiple hydro‐fracturing by boron‐rich fluids in the Late Miocene contact aureole of eastern Elba Island (Tuscany,Italy)

In eastern Elba Island (Tuscany, Italy), a shallow crustal level felsic, tourmaline‐bearing, dyke‐sill swarm of Late Miocene age is associated with abundant tourmaline‐quartz hydrothermal veins and metasomatic masses. Development of these veins and masses in the host rocks demonstrates multiple hydro‐fracturing by magmatic, boron‐rich saline fluid. Tourmalines in felsic dykes are schorl, whereas in veins and metasomatic masses, tourmaline composition ranges from schorl‐dravite through dravite to uvite. This compositional shift is evidence for an increasing contribution to the magmatic boron‐rich fluids by a Mg‐Ca‐Ti‐rich external component represented by biotite‐rich and amphibolite host rocks. This system can be envisaged as an exposed proxy of the high temperature hydrothermal system presently active in the deepest part of the Larderello‐Travale geothermal field (Tuscany).     

Mineralogical and geochemical studies of boron-rich bauxite ore deposits in the Songqi region,SW Henan,China

The Songqi region, SW Henan, is an important bauxite province in China. The bauxite ore deposits occur unconformably on the top of Middle Ordovician argillaceous carbonates. The bauxite ores from the Songqi region are characterized by unusually high boron contents. In this paper, we report the mineralogical and chemical compositions of selected bauxite ores from the region. These new data, together with existing geochemical data of soils in the region, are used to evaluate the origin of boron enrichment in the bauxite ores. The compositional characteristics of tourmaline in the bauxite ores suggests that this mineral was likely derived from a meta-sedimentary protolith. Mass balance calculation reveals that tourmaline only accounts for a small portion of boron in the bauxite ores; the majority of boron in the ores must occur in other forms, possibly by ion absorption on the surfaces of diaspore and clay minerals. In the Songqi region, the Precambrian meta-sedimentary rocks are known to contain abundant tourmalines whereas the Cambrian–Ordovician argillaceous carbonates and the Upper Proterozoic shales are all enriched in boron in free ion state. We suggest that these rocks provided tourmaline and boron ion to the bauxite deposits in the region. Most known bauxite deposits in the Songqi region occur at the margins of boron-rich soil domains, suggesting that boron in soils is a potential exploration indicator for unknown bauxite deposits in this region.     

Late magmatic – hydrothermal tourmaline occurrences within leucogranites in NW Anatolia (Turkey): Mineral chemistry and genetic implications

Numerous Oligo-Miocene plutonic and associated aplite-pegmatite rocks occur in the Western Anatolian Magmatic Complex. However, only the plutons of Namazgah, Karadağ, Soğucak and Karadoru, in the Biga Peninsula, host three different types of tourmaline: disseminated, nodular, and vein-type. These all fall into the alkali subgroup and schorl-oxy-schorl-dravite-oxy-dravite solid solution series. This study shows they were formed during late magmatic to hydrothermal stages in the roof sections (at shallow crustal levels) of the granitoid intrusions. Tourmaline compositions remained fairly homogeneous during the formation and evolution of each stage.     

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     

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.     

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。     

Chemical and boron-isotope variations in tourmalines from an S-type granite and its source rocks: the Erongo granite and tourmalinites in the Damara Belt,Namibia

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.     

The low-pressure partial-melting behaviour of natural boron-bearing metapelites from the Mt. Stafford area,central Australia

This study has examined the ~300 MPa partial melting behaviour of four metapelites collected from the highest grade rocks occurring below the anatectic zone of the Mt. Stafford area, Arunta Inlier, central Australia. In this area, metasediments are interpreted to have undergone partial melting within the andalusite stability field; possibly as a result of a lowering of the metapelite solidus by the presence of boron in the rocks. Two of the samples were two mica metapelites (MTS70 and MTS71). These both contained significant quantities of tourmaline and were thus boron enriched. The other two samples are biotite metapelites. One of these rocks contains only a trace of tourmaline (MTS8) and the other is tourmaline free (MTS7). Despite expectations that muscovite in the two mica samples would break down via a subsolidus reaction, muscovite was stable to above 750°C due to the incorporation of Ti, phengitic and possibly F components into its structure. Between 750 and 800°C, muscovite melted out completely via a coupled muscovite + biotite fluid-absent incongruent reaction. Tourmaline was partially consumed in this reaction, with the elbaitic component being preferentially consumed. In the most mica-rich sample this reaction produced ~60% melt at 800°C. In the biotite metapelites, biotite melting began at a temperature below 800°C and was accompanied by very modest melt production at this low temperature. In contrast to the two mica metapelites, the main pulse of melt production in these samples occurred at a temperature between 850 and 950°C. In both these samples biotite + melt coexisted over a temperature range in excess of 150°C, and in MTS8, biotite was still in the run products at 950°C. The very refractory nature of these evolved biotite compositions is most likely a consequence of both the presence of a Ti buffering phase in the assemblage (ilmenite) and the essentially plagioclase-free nature of the starting compositions. Under the fluid-absent conditions of this study, tourmaline is clearly a reactant in the partial melting process, but does not appear to shift the fluid-absent incongruent melting reactions markedly. In the tourmaline-rich two mica metapelites, tourmaline only disappears from the run products at a temperature above 850°C, where it coexisted with a substantial melt proportion. This appears to coincide with the point of maximum boron concentration in the melts.

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Using estimated thermodynamic properties to model accessory phases: the case of tourmaline

Accessory phases and minor components in minerals are commonly ignored in thermodynamic modelling. Such an approach seems unwarranted, as accessory phases can represent a significant element reservoir and minor components can substantially change their host mineral's stability field. However, a lack of thermodynamic data prohibits assessment of these effects. In this contribution, the polyhedron method is used to estimate the thermodynamic properties of tourmaline, a common and widespread accessory phase, stable over a range of P–T–X conditions. The polyhedron method allows Δ H , S , V , C _P and V _m ( T , P ) properties to be estimated from a linear stoichiometric summation over the fractional properties of its polyhedron constituents. To allow for estimates of tourmaline, fractional thermodynamic properties for B^III and B^IV polyhedra were derived. Mixing contributions to molar volume were evaluated and symmetrical mixing parameters derived for Al-Mg, Al-Fe and Al-Li interaction on tourmaline's Y-site and T-site Al-Si interaction. Evaluation of the estimated properties using experimental and natural equilibria between tourmaline and melts, minerals and hydrothermal fluids, shows that reliable semi-quantitative results are obtained. The boron contents in fluids coexisting with tourmaline are calculated to within an order of magnitude of measured content, and where anchor-points are available, agreement improves to within a factor of 2. Including tourmaline in petrogenetic modelling of metamorphic rocks indicates that its presence leads to disappearance of staurolite and garnet, among others, and modifies the X _Mg of coexisting phases, in line with observations on natural rocks.     

辽东裂谷带硫化物矿床内电气石系列矿物学与找矿关系

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。     

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