Corundum-bearing metasomatic rocks in the Central Pamirs

The Muzkol metamorphic complex in the Central Pamirs contains widespread occurrences of corundum mineralization, sometimes with gem-quality corundum. These occurrences are spatially related to zones of metasomatic alterations in calcite and dolomite marbles and crystalline schists. The calcite marbles contain corundum together with muscovite, scapolite, and biotite; the dolomite marbles contain corundum in association with biotite; and the schists bear this mineral coexisting with biotite and chlorite. All these rocks additionally contain tourmaline, apatite, rutile, and pyrite. The biotite is typically highly aluminous (up to 1.9 f.u. Al), and the scapolite is rich in the marialite end member (60–75 mol %). The crystallization parameters of corundum were estimated using mineral assemblages at T = 600–650°C, P = 4–6 kbar, X _{CO 2} = 0.2–0.5 at elevated alkalinity of the fluid. The Sr concentration in the calcite and dolomite marbles is low (345–460 and 62–110 ppm, respectively), as is typical of recrystallized sedimentary carbonates. The variations in the ⁸⁷Sr/⁸⁶Sr ratio in the calcite and dolomite marbles (0.70852–0.70999 and 0.70902–0.71021, respectively) were controlled by the introduction of radiogenic ⁸⁷Sr during the metasomatic transformations of the rocks. The isotopic-geochemical characteristics obtained for the rocks and the results of numerical simulations of the fluid-rock interactions indicate that the corundum-bearing metasomatic rocks developed after originally sedimentary Phanerozoic carbonate rocks, with the desilication of the terrigenous material contained in them. This process was a manifestation of regional alkaline metasomatism during the closing stages of Alpine metamorphism. In the course of transformations in the carbonate reservoir, the juvenile fluid flow became undersaturated with respect to silica, which was a necessary prerequisite for the formation of corundum.     

Mineralogy and metasomatic evolution of the Mianeh iron skarn deposit,Norduz-Agarak border,NW Iran

The Mianeh iron skarn deposit lies in the Arasbaran region within the Qaradagh metallogenic district, NW Iran. This high-grade massive magnetite skarn originated by the interaction of Upper Cretaceous limestone with metasomatic ore-bearing fluids associated with hypabyssal Oligo-Miocene quartz diorite. Mineral chemistry of the primary clinopyroxenes demonstrates the sub-alkaline, volcanic arc setting of magmatism. Two general stages of skarnification are recognized: (1) silicate skarn (stage I) is composed essentially of grossular and low-Fe diopside formed before the main mineralization and (2) magnetite-garnet skarn (stage II) composed of strongly anisotropic coarse-grained garnets with a narrow compositional zoning radially formed by addictive infiltrating of silica and iron-rich metasomatic fluids which overprint and/or crosscut the early stage silicate skarn. Anhydrous prograde calc-silicate assemblages were replaced by a series of hydrous calc-silicates (epidote, tremolite-actinolite) and/or quartz, calcite, magnetite, hematite, and pyrite. Magnetite (±hematite) is the dominant hypogene ore mineral that initially precipitated coincident with the late prograde to the early retrograde metasomatic stages. Mineralogical studies suggest that silicate skarn formation commenced at temperatures about 560 °C, X(CO₂)_fluid ≤ 0.15, αSiO₂～?1.0, and fluid pressure 1.0 kbar. The magnetite-garnet skarn formed from H₂O-rich fluids [X(CO₂)_fluid < 0.1] at a temperature of 525 to 450 °C and maximum log ?O₂ between ?20.2 and ?23. During the late stages of prograde skarn development, the stability field of andradite shifted to low ?O₂ and ?S₂ conditions resulting in main iron ore deposition (as magnetite). The andradite replacement temperature and presence of pyrite (instead of pyrrhotite) suggest that log?S₂ remained constant at about ?6 to ?7 during cooling of the system.     

Metasomatism and ore formation at contacts of dolerite with saliferous rocks in the sedimentary cover of the southern Siberian platform

The data on the mineral composition and crystallization conditions of magnesian skarn and magnetite ore at contacts of dolerite with rock salt and dolomite in ore-bearing volcanic—tectonic structures of the Angara—Ilim type have been integrated and systematized. Optical microscopy, scanning and transmission electron microscopy, electron microprobe analysis, electron paramagnetic resonance, Raman and IR spectroscopy, and methods of mineralogical thermometry were used for studying minerals and inclusions contained therein. The most diverse products of metasomatic reactions are found in the vicinity of a shallow-seated magma chamber that was formed in Lower Cambrian carbonate and saliferous rocks under a screen of terrigenous sequences. Conformable lodes of spinel-forsterite skarn and calciphyre impregnated with magnesian magnetite replaced dolomite near the central magma conduit and apical portions of igneous bodies. At the postmagmatic stage, the following mineral assemblages were formed at contacts of dolerite with dolomite: (1) spinel + fassaite + forsterite + magnetite (T = 820?740°C), (2) phlogopite + titanite + pargasite + magnetite (T = 600–500°C), And (3) clinochlore + serpentine + pyrrhotite (T = 450°C and lower). Rock salt is transformed at the contact into halitite as an analogue of calciphyre. The specific features of sedimentary, contact-metasomatic, and hydrothermal generations of halite have been established. The primary sedimentary halite contains solid inclusions of sylvite, carnallite, anhydrite, polyhalite, quartz, astrakhanite, and antarcticite; nitrogen, methane, and complex hydrocarbons have been detected in gas inclusions; and the liquid inclusions are largely aqueous, with local hydrocarbon films. The contact-metasomatic halite is distinguished by a fine-grained structure and the occurrence of anhydrous salt phases (CaCl₂ · KCl, CaCl₂, nMgCl₂ · mCaCl₂) and high-density gases (CO₂, H₂S, N₂, CH₄, etc.) as inclusions. The low-temperature hydrothermal halite, which occurs in skarnified and unaltered silicate rocks and in ore, is characterized by a low salinity of aqueous inclusions and the absence of solid inclusions. The composition and aggregative state of inclusions in halite and forsterite indicate that salt melt-solution as a product of melting and dissolution of salt was the main agent of high-temperature metasomatism. Its total salinity was not lower than 60%. The composition and microstructure of magnetite systematically change in different mineral assemblages. Magnetite is formed as a result of extraction of iron together with silicon and phosphorus from dolerite. The first generation of magnetite is represented by mixed crystals, products of exsolution in the Fe-Mg-Al-Ti-Mn-O system. The Ti content is higher at the contact of dolerite with rock salt, whereas, at the contact with dolomite, magnetite is enriched in Mg. The second generation of magnetite does not contain structural admixtures. The distribution of boron minerals and complex crystal hydrates shows that connate water of sedimentary rocks could have participated in hydrothermal metasomatic processes.     

Physicochemical model for the crystallization of rocks of the calc-alkaline series

The Al-rich region of the CaO-MgO-Al₂O₃-SiO₂ system was experimentally studied at pressures of 1.0–2.8 GPa and temperatures of 1300–1535°C. The slopes of the lines of the monovariant reactions An + Sp = Cpx + Cor + (Ga) and L = Cpx + Ga + Cor + Sp and the compositions of the phases involved in these reactions are determined. The results are utilized in the topological analysis of the aluminous region of the CaO-MgO-Al₂O₃-SiO₂ system. On this basis, the principal structure of the phase diagram is analyzed, and a phase diagram is constructed for the junction region of the quaternary system and the CaO-Al₂O₃-SiO₂ ternary system. A continuous series of the monovariant eutectic: L = Cpx + Opx + Fo + An, L = Cpx + Opx + An + Sp, L = Cpx + (Ga) + An + Sp, L = Cpx + Cor + (Ga) + An, L = An + Ga + Cpx + Ky and L = Ga + Cpx + Ky + Qz is examined within the pressure range from atmospheric to 3.0 GPa and higher. Analogous “telescoped” eutectic series are of fundamental character for interpreting the evolution of magmatic melts. A physicochemical model is suggested for the evolution of magmatic melts that produce rocks of the calc-alkaline series, with this model underlain by the fact that a change in the composition of magmatic melt at a pressure decrease should correspond to the minimum melting temperatures, i.e., to melts in the fundamental series of eutectic reactions. The comparison of our physicochemical model and rocks of the calc-alkaline series shows that the compositions of rocks of the calc-alkaline series are close to the compositions determined for the eutectic equilibria, and the mineralogical composition of xenoliths and megacrysts in volcanic and dike varieties of the rocks are similar to the subsolidus phases of the established fundamental eutectic system.     

Metasomatism of ferroan granites in the northern Aravalli orogen,NW India: geochemical and isotopic constraints,and its metallogenic significance

The late Palaeoproterozoic (1.72–1.70 Ga) ferroan granites of the Khetri complex, northern Aravalli orogen, NW India, were extensively metasomatised ~900 Ma after their emplacement, at around 850–830 Ma by low-temperature (ca. 400 °C) meteoric fluids that attained metamorphic character after exchanging oxygen with the surrounding metamorphic rocks. Albitisation is the dominant metasomatic process that was accompanied by Mg and Ca metasomatism. A two-stage metasomatic model is applicable to all the altered ferroan intrusives. The stage I is represented by a metasomatic reaction interface that developed as a result of transformation of the original microcline–oligoclase (An_12–14) granite to microcline–albite (An_1–3) granite, and this stage is rarely preserved. In contrast, the stage II metasomatic reaction front, where the microcline-bearing albite granite has been transformed to microcline-free albite granite, is readily recognisable in the field and present in most of the intrusives. Some of them lack an obvious reaction interface due to the presence of stage II albite granites only. When studied in isolation, these intrusives were incorrectly classified and their tectonic setting was misinterpreted. Furthermore, our results show that the mafic mineralogy of metasomatised granites has a significant impact on the characterisation of such rocks in the magmatic classification and discrimination diagrams. Nevertheless, the stage I metasomatised granites can be appropriately characterised in these diagrams, whereas the characterisation of the stage II granites will lead to erroneous interpretations. The close spatial association of these high heat producing ferroan granites with iron oxide–copper–gold (IOCG), U and REE mineralisation in the region indicates a genetic link between the metasomatism and the mineralisation. World-class IOCG, U and REE deposits are associated with metasomatised ferroan granites, suggesting that such a relationship may act as a critical first-order exploration target for undiscovered mineral deposits.     

The world-class Natalka gold deposit, northeast Russia: REE patterns, fluid inclusions, stable oxygen isotopes, and formation conditions of ore

REE patterns of hydrothermally altered rocks, fluid inclusions, and stable oxygen isotopes of quartz were studied at the Natalka gold deposit. Metasomatic rocks formed under decompression reveal gradual depletion in LREE and HREE relative to siltstone of the protolith. The HREE patterns of metasomatic rocks formed under decompression are uniform; an insignificant removal of LREE can be noted. The progressive extraction of REE with increasing alteration of rocks could have been due to the effect of magmatogenic or meteoric fluid. Because a Ce anomaly is absent, the participation of oxidized meteoric water was limited. The inverse correlation between the total REE content and the Eu anomaly value in altered rocks indicates a substantial role of magmatogenic fluid. The REE patterns of altered rocks formed under compression show that the role of metamorphic fluid was not great. All metasomatic rocks are enriched in LREE, so that the enrichment of fluid in LREE as well may be suggested. Three fluid compositions were captured as fluid inclusions: (1) H₂O-CO₂-NaCl-MgCl₂ with a salinity of 1.0–4.9 wt % NaCl equiv, (2) CO₂-CH₄, and (3) H₂O-NaCl-MgCl₂ with a salinity of 7.0–5.6 wt % NaCl equiv. Compositions (1) and (2) coexisted in the mineral-forming system at 250–350°C and 1.1–2.4 kbar as products of phase separation under conditions of decreasing P and T. The interaction of this fluid with host rocks resulted in the formation of extensive halos of beresitized rocks with sulfide disseminations. The precipitation of arsenopyrite and pyrite led to the substantial depletion of mineral-forming fluid in H₂S and destabilization of the Au(HS)^2? complex. The fluid with the third composition arose due to the boiling of the H₂O-CO₂-CH₄-NaCl-MgCl₂ liquid and was responsible for metasomatic alteration of host rocks. The late mineral assemblages were deposited from this fluid at the initial stage of ore formation. The high methane concentrations in the ore-forming fluid were likely caused by interaction of hydrothermal ore-bearing solutions with carbonaceous host rocks. The δ¹⁸O values of quartz from quartz-scheelite-pyrite-arsenopyrite and sulfide-sulfosalt mineral assemblages vary from +11.6 to +14.1‰ and +11.2 to +13.5‰, respectively. The parental fluids of the early and late mineral assemblages probably were derived from a magmatic source and were characterized by $ \delta ^{18} O_{H_2 O} REE patterns of hydrothermally altered rocks, fluid inclusions, and stable oxygen isotopes of quartz were studied at the Natalka gold deposit. Metasomatic rocks formed under decompression reveal gradual depletion in LREE and HREE relative to siltstone of the protolith. The HREE patterns of metasomatic rocks formed under decompression are uniform; an insignificant removal of LREE can be noted. The progressive extraction of REE with increasing alteration of rocks could have been due to the effect of magmatogenic or meteoric fluid. Because a Ce anomaly is absent, the participation of oxidized meteoric water was limited. The inverse correlation between the total REE content and the Eu anomaly value in altered rocks indicates a substantial role of magmatogenic fluid. The REE patterns of altered rocks formed under compression show that the role of metamorphic fluid was not great. All metasomatic rocks are enriched in LREE, so that the enrichment of fluid in LREE as well may be suggested. Three fluid compositions were captured as fluid inclusions: (1) H₂O-CO₂-NaCl-MgCl₂ with a salinity of 1.0–4.9 wt % NaCl equiv, (2) CO₂-CH₄, and (3) H₂O-NaCl-MgCl₂ with a salinity of 7.0–5.6 wt % NaCl equiv. Compositions (1) and (2) coexisted in the mineral-forming system at 250–350°C and 1.1–2.4 kbar as products of phase separation under conditions of decreasing P and T. The interaction of this fluid with host rocks resulted in the formation of extensive halos of beresitized rocks with sulfide disseminations. The precipitation of arsenopyrite and pyrite led to the substantial depletion of mineral-forming fluid in H₂S and destabilization of the Au(HS)²⁻ complex. The fluid with the third composition arose due to the boiling of the H₂O-CO₂-CH₄-NaCl-MgCl₂ liquid and was responsible for metasomatic alteration of host rocks. The late mineral assemblages were deposited from this fluid at the initial stage of ore formation. The high methane concentrations in the ore-forming fluid were likely caused by interaction of hydrothermal ore-bearing solutions with carbonaceous host rocks. The δ¹⁸O values of quartz from quartz-scheelite-pyrite-arsenopyrite and sulfide-sulfosalt mineral assemblages vary from +11.6 to +14.1‰ and +11.2 to +13.5‰, respectively. The parental fluids of the early and late mineral assemblages probably were derived from a magmatic source and were characterized by = +6.3 to +8.8‰ at 350°C and +3.6 to +5.9‰ at 280°C, respectively. The narrow interval of oxygen isotopic compositions shows that this source was homogeneous. The data obtained allow us to suggest that the deposit formation was related to magmatic activity, including the direct supply of ore components from a magma chamber and mobilization of these components in the processes of dehydration and decarbonation during contact and regional metamorphism. Original Russian Text ? N.A. Goryachev, O.V. Vikent’eva, N.S. Bortnikov, V.Yu. Prokof’ev, V.A. Alpatov, V.V. Golub, 2008, published in Geologiya Rudnykh Mestorozhdenii, 2008, Vol. 50, No. 5, pp. 414–444.     

Origin of peraluminous minerals (corundum,spinel, and sapphirine) in a highly calcic anorthosite from the Sittampundi Layered Complex,Tamil Nadu,India

The highly calcic anorthosite (An_>95) from the Sittampundi Layered Complex (SLC) develops corundum, spinel and sapphirine that are hitherto not reported from any anorthositic rocks in the world. Petrological observations indicate the following sequence of mineral growth: plagioclase_matrix → corundum; clinopyroxene → amphibole; corundum + amphibole → plagioclase_corona + spinel; and spinel + corundum → coronitic sapphirine. Phase relations in the CaO–Na₂O–Al₂O₃–SiO₂–H₂O (CNASH) system suggest that corundum was presumably developed through vapour present incongruent melting of the highly calcic plagioclase during ultra-high temperature (UHT) metamorphism (T ≥ 1000 °C, P ≥ 9 kbar). Topological constraints in parts of the Na₂O–CaO–MgO–Al₂O₃–SiO₂–H₂O (NCMASH) system suggest that subsequent to the UHT metamorphism, aqueous fluid(s) permeated the rock and the assemblage corundum + amphibole + anorthite + clinozoisite was stabilized during high-pressure (HP) metamorphism (11 ± 2 kbar, 750 ± 50 °C). Constraints of the NCMASH topology and thermodynamic and textural modeling study suggest that coronitic plagioclase and spinel formed at the expense of corundum + amphibole during a steeply decompressive retrograde P–T path (7–8 kbar and 700–800 °C) in an open system. Textural modeling studies combined with chemical potential diagrams (μSiO₂–μMgO) in the MASH system support the view that sapphirine also formed from due to silica and Mg metasomatism of the precursor spinel ± corundum, on the steeply decompressive retrograde P–T path, prior to onset of significant cooling of the SLC. Extremely channelized fluid flow and large positive solid volume change of the stoichiometrically balanced sapphirine forming reaction explains the localized growth of sapphirine.     

Genesis of garnet-bearing rocks at the Berezitovoe deposit,Upper Amur Region,Russia

The geological position, composition of mineral assemblages, and typomorphism of major minerals from garnet-bearing rocks at the Berezitovoe gold-base-metal deposit in the Upper Amur Region have been studied in detail. These are ore-bearing metasomatic rocks and metamorphosed porphyritic dikes. The garnet-bearing metasomatic rocks reveal zoning, which is caused by various degrees of metasomatic transformation of the Paleozoic porphyritic granodiorite that hosts the ore zone. The metasomatic replacement of granodiorite was accompanied by loss of Na, Ca, Ba, Sr and gain of K, Mn, and Rb. Garnet-bearing metamorphosed intermediate dikes occur within the metasomatic zone. The PT conditions of metamorphism and metasomatism are similar and estimated at 3.9 kbar and 500°C from various mineral equilibria. The results of physicochemical simulation of garnet-bearing mineral assemblages carried out by minimizing the Gibbs free energy and the geological data show that garnet-bearing mineral assemblages arose at the Berezitovoe deposit as a result of local high-temperature thermal metamorphism of previously formed low-temperature metasomatic rocks close in composition to classic beresite. In this connection, we propose considering garnet-bearing metasomatic rocks as high-temperature metamorphosed beresites.     

Lithological subdivision and petrology of the Great Himalayan Vaikrita Group in Kumaun,India

The Vaikrita Group made up of coarse mica-garnet-kyanite and sillimanite-bearing psammitic metamorphics constituting the bulk of the Great Himalaya in Kumaun is divisible into four formations, namely theJoshimath comprising streaky, banded psammitic gneisses and schists, the Pandukeshwar consisting predominantly of quartzite with intercalations of schists, thePindari made up of gneisses and schists with lenses of calc-silicate rocks and overwhelmingly injected by Tertiary pegmatites and granites (Badrinath Granite) leading to development of migmatites, and theBudhi Schist comprising biotite-rich calc-schists. The Vaikrita has been thrust along the Main Central Thrust over the Lesser Himalayan Munsiari Formation made up of highly mylonitized low-to meso-grade metamorphics, augen gneisses and phyllonites. Petrological studies demonstrate contrasting nature of metamorphism experienced by the Vaikrita and the Munsiari rocks. Sillimanite-kyanite-garnet-biotite-muscovite (±K-feldspar and ± plagioclase).—quartz metapelites and interbanded calc-schists and calc-gneisses with mineral assemblages of calcite-hornblende-grossular garnet, labradorite (An₅₀?An₆₅), (± K-feldspar)-quartz (± biotite), and hornblende-diopside ± labradorite ± quartz, suggest medium to high grade of metamorphism or indicate upper amphibolite facies experienced by the rocks of the Vaikrita Group. The associated migmatites, granite-gneisses and granites of the Pindari Formation were formed largely as a result of anatexis of metapelites and metapsammites. While, the sericite-chlorite-quartz and muscovite-chlorite-chloritoid-garnet-quartz, assemblages in metapelites and epidote-actinolite-oligoclase (An₂₀)-quartz and epidote-hornblende-andesine (An₂₉) ± quartz in the metabasites suggest a low-grade metamorphism (greenschist facies) for the Munsiari Formation, locally attaining the lower limit of medium-grade (epidote-amphibolite) facies. The inferred P-T conditions obtained from textural relations of various mineral phases and the stability relationship of different coexisting phases in equilibrium, suggest that the temperature ranged between 600° and 650° C and pressure was over 5 kb for the Vaikrita rocks. The mineral assemblages of the Munsiari Formation indicate comparatively lower P-T conditions, where the temperature reached approximately 450° C and pressure was near 4 kb. The rocks of the two groups were later subjected to intense shearing, cataclasis and attendant retrograde metamorphism within the zone of the Main Central (=Vaikrita) Thrust.     

Mineralogy and geochemistry of granitoids from Kinnaur region,Himachal Higher Himalaya,India: Implication on the nature of felsic magmatism in the collision tectonics

Felsic magmatism in the southern part of Himachal Higher Himalaya is constituted by Neoproterozoic granite gneiss (GGn), Early Palaeozoic granitoids (EPG) and Tertiary tourmaline-bearing leucogranite (TLg). Magnetic susceptibility values (<3 ×10^?3 SI), molar Al₂ O ₃/(CaO + Na₂ O + K ₂O) (≥1.1), mineral assemblage (bt–ms–pl–kf–qtz ± tur ± ap), and the presence of normative corundum relate these granitoids to peraluminous S-type, ilmenite series (reduced type) granites formed in a syncollisional tectonic setting. Plagioclase from GGn (An₁₀–An₃₁) and EPG (An₁₅–An₃₃) represents oligoclase to andesine and TLg (An₂–An₁₅) represents albite to oligoclase, whereas compositional ranges of K-feldspar are more-or-less similar (Or₈₈ to Or₉₅ in GGn, Or₈₆ to Or₉₇ in EPG and Or₈₇ to Or₉₄ in TLg). Biotites in GGn (Mg/Mg + Fe^t= 0.34–0.45), EPG (Mg/Mg + Fe^t= 0.27–0.47), and TLg (Mg/Mg + Fe^t= 0.25–0.30) are ferribiotites enriched in siderophyllite, which stabilised between FMQ and HM buffers and are characterised by dominant 3Fe\(\rightleftharpoons \)2Al, 3Mg\(\rightleftharpoons \)2Al substitutions typical of peraluminous (S-type), reducing felsic melts. Muscovite in GGn (Mg/Mg + Fe^t=0.58–0.66), EPG (Mg/Mg + Fe^t=0.31?0.59), and TLg (Mg/Mg + Fe^t=0.29–0.42) represent celadonite and paragonite solid solutions, and the tourmaline from EPG and TLg belongs to the schorl-elbaite series, which are characteristics of peraluminous, Li-poor, biotite-tourmaline granites. Geochemical features reveal that the GGn and EPG precursor melts were most likely derived from melting of biotite-rich metapelite and metagraywacke sources, whereas TLg melt appears to have formed from biotite-muscovite rich metapelite and metagraywacke sources. Major and trace elements modelling suggest that the GGn, EPG and TLg parental melts have experienced low degrees (～13, ～17 and ～13%, respectively) of kf–pl–bt fractionation, respectively, subsequent to partial melting. The GGn and EPG melts are the results of a pre-Himalayan, syn-collisional Pan-African felsic magmatic event, whereas the TLg is a magmatic product of Himalayan collision tectonics.     

Assemblages and genesis of platinum-group minerals in low-sulfide ores of the monchetundra deposit,Kola Peninsula,Russia

New data on the composition, assemblages, and formation conditions of platinum-group minerals (PGM) identified in platinum-group element (PGE) occurrences of the Monchetundra intrusion (2495 +- 13 to 2435 ± 11 Ma) are described. This intrusion is a part of the Paleoproterozoic pluton of the Monche-Chuna-Volch’i and Losevy tundras located in the Pechenga-Imandra-Varzuga Rift System. The rhythmically layered host rocks comprise multiple megarhythms juxtaposed to mylonite zones and magmatic breccia and injected by younger intrusive rocks in the process of intense and long magmatic and fluid activity in the Monchetundra Fault Zone. The primary PGM and later assemblages that formed as a result of replacement of the former have been identified in low-sulfide PGE occurrences. More than 50 minerals and unnamed PGE phases including alloys, Pt and Pd sulfides and bismuthotellurides, PGE sulfarsenides, and minerals of the Pd-As-Sb, Pd-Ni-As, and Pd-Ag-Te systems have been established. The unnamed PGE phases—Ni₆Pd₂As₃, Pd₆AgTe₄, Cu₃Pt, Pd₂NiTe₂, and (Pd, Cu)₉Pb(Te, S)₄—are described. The primary PGM were altered due to the effect of several mineral-forming processes that resulted in the formation of micro- and nanograins of Pt and Pd alloys, sulfides, and oxides, as well as in the complex distribution of PGE, Au, and Ag mineral assemblages. New types of complex Pt and Pd oxides with variable Cu and Fe contents were identified in the altered ores. Pt and Pd oxides as products of replacement of secondary Pt-Pd-Cu-Fe alloys occur as zonal and fibrous nanoscale Pt-Pd-Cu-Fe-(±S)-O aggregates.     

Petrological and experimental evidence for differentiation of water-rich magmas beneath St. Kitts,Lesser Antilles

St. Kitts lies in the northern Lesser Antilles, a subduction-related intraoceanic volcanic arc known for its magmatic diversity and unusually abundant cognate xenoliths. We combine the geochemistry of xenoliths, melt inclusions and lavas with high pressure–temperature experiments to explore magma differentiation processes beneath St. Kitts. Lavas range from basalt to rhyolite, with predominant andesites and basaltic andesites. Xenoliths, dominated by calcic plagioclase and amphibole, typically in reaction relationship with pyroxenes and olivine, can be divided into plutonic and cumulate varieties based on mineral textures and compositions. Cumulate varieties, formed primarily by the accumulation of liquidus phases, comprise ensembles that represent instantaneous solid compositions from one or more magma batches; plutonic varieties have mineralogy and textures consistent with protracted solidification of magmatic mush. Mineral chemistry in lavas and xenoliths is subtly different. For example, plagioclase with unusually high anorthite content (An_≤100) occurs in some plutonic xenoliths, whereas the most calcic plagioclase in cumulate xenoliths and lavas are An₉₇ and An₉₅, respectively. Fluid-saturated, equilibrium crystallisation experiments were performed on a St. Kitts basaltic andesite, with three different fluid compositions (XH₂O = 1.0, 0.66 and 0.33) at 2.4 kbar, 950–1025 °C, and fO₂ = NNO ? 0.6 to NNO + 1.2 log units. Experiments reproduce lava liquid lines of descent and many xenolith assemblages, but fail to match xenolith and lava phenocryst mineral compositions, notably the very An-rich plagioclase. The strong positive correlation between experimentally determined plagioclase-melt Kd_Ca–Na and dissolved H₂O in the melt, together with the occurrence of Al-rich mafic lavas, suggests that parental magmas were water-rich (> 9 wt% H₂O) basaltic andesites that crystallised over a wide pressure range (1.5–6 kbar). Comparison of experimental and natural (lava, xenolith) mafic mineral composition reveals that whereas olivine in lavas is predominantly primocrysts precipitated at low-pressure, pyroxenes and spinel are predominantly xenocrysts formed by disaggregation of plutonic mushes. Overall, St. Kitts xenoliths and lavas testify to mid-crustal differentiation of low-MgO basalt and basaltic andesite magmas within a trans-crustal, magmatic mush system. Lower crustal ultramafic cumulates that relate parental low-MgO basalts to primary, mantle -derived melts are absent on St. Kitts.     

Metaultramafic schists and dismembered ophiolites of the Ashe Metamorphic Suite of northwestern North Carolina,USA

ABSTRACT

Metaultramafic rocks (MUR) in the Ashe Metamorphic Suite (AMS) of northwestern North Carolina include quartz ± feldspar-bearing QF-amphibolites and quartz-deficient, locally talc-, chlorite-, and/or Mg-amphibole-bearing TC-amphibolites. Some workers divide TC-amphibolites into Todd and Edmonds types, based on mineral and geochemical differences, and we provisionally add a third type – olivine ± pyroxene-rich, Rich Mountain-type rocks. Regionally, MUR bodies range from equant, Rich Mountain- to highly elongate, Todd-TC-amphibolite-type bodies. The MURs exhibit three to five mineral associations containing assemblages with olivine, anthophyllitic amphibole, Mg-hornblende, Mg-actinolite, cummingtonite, and serpentine representing decreasing eclogite to greenschist facies grades of metamorphism over time. MUR protoliths are difficult to determine. Southwestern MUR bodies have remnant olivine ± pyroxene-rich assemblages representing ultrabasic-basic, dunite-peridotite-pyroxenite protoliths. Northeastern TC-amphibolite MURs contain hornblende and actinolitic amphiboles plus chlorites – aluminous and calcic assemblages suggesting to some that metasomatism of basic, QF-amphibolites yields all TC-amphibolites. Yet MgO-CaO-Al₂O₃ and trace element chemistries of many TC-amphibolites resemble compositions of plagioclase peridotites. We show that a few AMS TC-amphibolites had basaltic/gabbroic protoliths, while presenting arguments opposing application of the metasomatic hypothesis to all TC-amphibolites. We establish that MUR bodies are petrologically heterolithic and that TC-amphibolites are in contact with many rock types; that those with high Cr, Ni, and Mg have olivine- or pyroxene-dominated protoliths; that most exhibit three or more metamorphic mineral associations; and that contacts thought to be metasomatic are structural. Clearly, different MUR bodies have different chemistries representing various protoliths, and have different mineral assemblages, reflecting both chemical composition and metamorphic history. Spot sampling of heterolithic MUR bodies does not reveal MUR body character or history or allow ‘type’ designations. We recommend that the subdivision of MUR bodies into ‘types’ be abandoned and that the metasomatic hypothesis be carefully applied. AMS MURs and associated metamafic rocks likely represent fragments of dismembered ophiolites from various ophiolite types.     

FEG-EPMA mapping and Fe-Ti oxide mineral chemistry of Brahmaputra River sediments in Bangladesh: provenance and petrogenetic implications

The present research deals with the FEG-EPMA mapping and Fe-Ti oxide mineral chemistry of Brahmaputra River sediments in Bangladesh. Major heavy minerals in the sediments consist of garnet (8.5–21.3%), kyanite (5.35–11.9%), monazite (2.3–5.3%), sillimanite (1.8–4.7%), zircon (3.6–9.1%), and a considerable amount of opaques mainly Fe-Ti oxide minerals (23.1–35.4%). The detrital Fe-Ti oxide minerals carry significant clues to the parent rocks or sources. In these contexts, detrital opaques (Fe-Ti oxides) have been analyzed with an electron probe microanalyzer (EPMA). These opaques (Fe-Ti oxide) display six types of textural patterns, dominantly seriate with granular, emulsion, and acicular sandwich structures and trellis type of textural patterns. These textural patterns belong to five intergrowths of Fe-Ti oxide minerals such as (1) ilmenite-hematite, (2) magnetite-ilmenite, (3) hematite-rutile, (4) ilmenite-hematite-rutile, and (5) ilmenite-rutile, where ilmenite-hematite intergrowth is common. Alteration is seen in both exsolved and unexsolved ilmenites. Textural patterns and mineral chemistry of the studied ilmenite minerals provide lines of evidence of low-temperature magmatic inheritance, later modified by diffusional processes. The estimated temperature and oxygen fugacity from the magnetite-ilmenite exsolution range from 547.6 to 558.2 °C and from 10^?21.4 to 10^?21.7, respectively. The data are also consistent with hematite-ilmenite temperature (between 537 and 540 °C) and oxygen fugacity (10^?21.7 to 10^?21.9) measurements in Cox’s Bazar beach placers. These temperatures and oxygen fugacities specify Fe-Ti oxide assemblages equilibrated in a T-fO₂ field very near to the FMQ buffer curve suggesting a crustal source (magmatic and/or metamorphic), which is modified significantly by metamorphic processes.     

P–T–fluid evolution in the Mahalapye Complex, Limpopo high-grade terrane, eastern Botswana

Metapelites, migmatites and granites from the c. 2 Ga Mahalapye Complex have been studied for determining the P–T–fluid influence on mineral assemblages and local equilibrium compositions in the rocks from the extreme southwestern part of the Central Zone of the Limpopo high‐grade terrane in Botswana. It was found that fluid infiltration played a leading role in the formation of the rocks. This conclusion is based on both well‐developed textures inferred to record metasomatic reactions, such as Bt ? And + Qtz + (K₂O) and Bt ± Qtz ? Sil + Kfs + Ms ± Pl, and zonation of Ms | Bt + Qtz | And + Qtz and Grt | Crd | Pl | Kfs + Qtz reflecting a perfect mobility (Korzhinskii terminology) of some chemical components. The conclusion is also supported by the results of a fluid inclusion study. CO₂ and H₂O ( = 0.6) are the major components of the fluid. The fluid has been trapped synchronously along the retrograde P–T path. The P–T path was derived using mineral thermobarometry and a combination of mineral thermometry and fluid inclusion density data. The Mahalapye Complex experienced low‐pressure granulite facies metamorphism with a retrograde evolution from 770 °C and 5.5 kbar to 560 °C and 2 kbar, presumably at c. 2 Ga.     

Orthopyroxene–sillimanite–quartz assemblages: distribution, petrology, quantitative P–T–X constraints and P–T paths

Granulite facies magnesian metapelites commonly preserve a wide array of mineral assemblages and reaction textures that are useful for deciphering the metamorphic evolution of a terrane. Quantitative pressure, temperature and bulk composition constraints on the development and preservation of characteristic peak granulite facies mineral assemblages such as orthopyroxene + sillimanite + quartz are assessed with reference to calculated phase diagrams. In NCKFMASH and its chemical subsystems, peak assemblages form mainly in high‐variance fields, and most mineral assemblage changes reflect multivariant equilibria. The rarity of orthopyroxene–sillimanite–quartz‐bearing assemblages in granulite facies rocks reflects the need for bulk rock X_Mg of greater than approximately 0.60–0.65, with pressures and temperatures exceeding c. 8 kbar and 850 °C, respectively. Cordierite coronas mantling peak minerals such as orthopyroxene, sillimanite and quartz have historically been used to infer isothermal decompression P–T paths in ultrahigh‐temperature granulite facies terranes. However, a potentially wide range of P–T paths from a given peak metamorphic condition facilitate retrograde cordierite growth after orthopyroxene + sillimanite + quartz, indicating that an individual mineral reaction texture is unable to uniquely define a P–T vector. Therefore, the interpretation of P–T paths in high‐grade rocks as isothermal decompression or isobaric cooling may be overly simplistic. Integration of quantitative data from different mineral reaction textures in rocks with varying bulk composition will provide the strongest constraints on a P–T path, and in turn on tectonic models derived from these paths.     

Aureoles of Songshugou Alpine-type ultramafic massif

The Songshugou Alpine-type ultramafic massif intruded into the surrounding plagioclase-amphibole schists where high-temperature aureoles are found well exposed but not distroyed. From the outer part inwards, four aureoles are recognized: the oligoclase-hornblende zone, the andesine-hornblende zone, the garnet zone and the pyroxene zone. Toward the massif, systematic variations are noticed in the rocks from one zone to another, i.e., the rocks vary from fine-grained, fibrous, crystalloblastic texture to medium coarse-grained, granular, crystalloblastic texture and from schistose structure to massive structure; hornblende varies from blue-green to brofn; plagioclases vary in composition from An_12–17 to An₃₇, even to An₆₀ near the contact; garnet and pyroxene become more and more abundant; sphene is replaced progressively by titanomagnetite; and Na(K), Al and Ti in the hornblende tend to increase near the contact. Studies have shown that the typical rocks in the four contact metamorphic zones are generally similar in major and trace elements. But different mineral assemblages and mineral chemistry indicate that the rocks were formed under different physical conditions.     

Luna 20 soil: abundance and composition of phases in the 45–125 micron fraction

Glass compositions in the Luna 20 soil indicate a minor contribution of mare rocks and a major contribution of highly feldspathic highland material. Glasses with the composition of Highland basalt (anorthositic gabbro or norite) predominate in a range of highly aluminous glasses.The analyses of minerals in the soil show that the highland rocks have a unique assemblage of minerals that can readily be distinguished from the mineral assemblages of either mare or KREEP basalts. The soils are characterized by abundant anorthitic (An_92–99), low-Fe plagioclase. Highly magnesian orthopyroxenes, pigeonites and augites are the most prominent pyroxenes. Unlike mare basalt pyroxenes, clinopyroxenes with intermediate Ca values are not abundant, but extreme iron enrichment towards pyroxferroite does occur. Olivines are more abundant than at other sites and are Mg-rich, low in Ca and Cr. Spinels with compositions approaching MgAl₂O₄ predominate over pleonastes and chromites. Ilmenite and metal are present but not abundant.These data establish the unique nature of the minerals in the highland soils. The mineral compositions are consistent with derivation from a suite of highly feldspathic rocks in which Highland basalt compositions predominate. Some of the mineral data, particularly from the pyroxenes, are suggestive of surface or near-surface processes, rather than plutonic crystallization.     

Experimental study of the influence of water on elastic wave velocities in dunite and serpentinite (on the nature of the low-velocity zone in the upper mantle of the Earth)

Longitudinal wave velocities (V _P ) in rocks were measured experimentally in dunite (olivinite) and serpentinite at a water pressure of 300 MPa and temperatures of 20–850°C. It is shown that the strong decrease in V _P in dunite (by ~3 km/s) observed within the range of 400–800°C results from penetration of water into rock along microfractures and from the formation of hydrous minerals (mostly serpentine) along the boundaries of mineral grains as a result of water–olivine interaction. It is suggested that serpentinization or the formation of similar hydrous minerals in olivine-rich mantle rocks under the influence of deep fluids may result in the formation of zones of low-velocity elastic waves in the upper mantle at great depths (~100 km).     

The Sr,Nd, and Hf isotopic geochemistry of rocks of the gabbro–diorite–tonalite association from the Eastern Segment of the Middle Urals as an indicator of the age of the continental crust in this area

According to isotopic analysis of rocks of the Reft gabbro–diorite–tonalite complex (Middle Urals), gabbro and related diorite and dikes and vein-shaped bodies of plagiogranitoids, crosscutting gabbro, are similar to the depleted mantle substance in ε_Nd(T) = 8.6–9.7 and ε_Hf(T) = 15.9–17.9. Their model Hf ages are correlated with the time of crystallization. Here, the tonalites and quartz diorites constituting most of the Reft massif are characterized by lower values: ε_Nd(T) = 3.7–6.0, ε_Hf(T) = 11.1–12.7, and T _DM values significantly exceeding the age datings. This is evidence that Neoproterozoic crustal rocks were a source of parental magma for these rocks. The primary ⁸⁷Sr/⁸⁶Sr ratio in rocks of both groups is highly variable (0.70348–0.70495). The data obtained allow us to reach the conclusion that the Reft gabbro–diorite–tonalite complex was formed as a result of nearly synchronous processes occurring in the crust and the mantle within a limited area.