Perthite microstructure in magmatic alkali feldspar with oscillatory zoning; Weinsberg Granite, Upper Austria

Feldspar megacrysts from the Weinsberg granite (Moldanubian Zone) show oscillatory zoning with respect to the albite- and orthoclase components. All growth zones show perthitic exsolutions which take the form of bleb- and lens shaped albite-rich precipitates in an orthoclase-rich host. The average sizes and shapes of the precipitates show systematic variation with the integrated bulk compositions of the respective growth zones. The precipitates are abundant and relatively small in growth zones with intermediate bulk composition (Or50Ab41An09 - Or80Ab18An02), and they are less abundant and larger in more orthoclase-rich zones (Or88Ab11An01). Small precipitates have a relatively high aspect ratio, whereas the large precipitates in the potassium-rich zones are more spherical. The relation between microstructure and integrated bulk composition suggests that exsolution and subsequent growth and coarsening occurred by different mechanisms in the respective growth zones. Numerical modeling shows that rapid growth of precipitates over extended periods of time and attainment of relatively large final size is favored, if only few nuclei are formed in an oversaturated host. In contrast, precipitates can grow rapidly only over limited time intervals and remain relatively small, if abundant nuclei are present. During cooling of the oscillatorily zoned alkali-feldspar, exsolution started at relatively high temperatures in growth zones of intermediate integrated bulk composition as compared to exsolution in the more orthoclase-rich growth zones. Irrespective of whether exsolution occurred by spinodal decomposition or by nucleation at relatively high temperatures in the growth zones of intermediate integrated bulk composition, it produced abundant nuclei and resulted in relatively small precipitates. In contrast, comparatively few nuclei were formed in the orthoclase-rich growth zones resulting in large precipitates. The Na/K partitioning between precipitates and the host is independent of the integrated bulk composition of the respective growth zone reflecting re-equilibration during cooling down to relatively low temperatures (<?400°C). The shape of the precipitates probably has evolved from an initially lamellar or spindle-like geometry with high aspect ratio to more isometric, spheroidal shapes during precipitate growth and coarsening. Host/precipitate interfaces served as fluid pathways during late stage deuteric alteration.     

Partial melting due to breakdown of an epidote‐group mineral during exhumation of ultrahigh‐pressure eclogite: An example from the North‐East Greenland Caledonides

In the North‐East Greenland Caledonides, P–T conditions and textures are consistent with partial melting of ultrahigh‐pressure (UHP) eclogite during exhumation. The eclogite contains a peak assemblage of garnet, omphacite, kyanite, coesite, rutile, and clinozoisite; in addition, phengite is inferred to have been present at peak conditions. An isochemical phase equilibrium diagram, along with garnet isopleths, constrains peak P–T conditions to be subsolidus at 3.4 GPa and 940°C. Zr‐in‐rutile thermometry on inclusions in garnet yields values of ~820°C at 3.4 GPa. In the eclogite, plagioclase may exhibit cuspate textures against surrounding omphacite and has low dihedral angles in plagioclase–clinopyroxene–garnet aggregates, features that are consistent with former melt–solid–solid boundaries and crystallized melt pockets. Graphic intergrowths of plagioclase and amphibole are present in the matrix. Small euhedral neoblasts of garnet against plagioclase are interpreted as formed from a peritectic reaction during partial melting. Polymineralic inclusions of albite+K‐feldspar and clinopyroxene+quartz±kyanite±plagioclase in large anhedral garnet display plagioclase cusps pointing into the host, which are interpreted as crystallized melt pockets. These textures, along with the mineral composition, suggest partial melting of the eclogite by reactions involving phengite and, to a large extent, an epidote‐group mineral. Calculated and experimentally determined phase relations from the literature reveal that partial melting occurred on the exhumation path, at pressures below the coesite to quartz transition. A calculated P–T phase diagram for a former melt‐bearing domain shows that the formation of the peritectic garnet rim occurred at 1.4 GPa and 900°C, with an assemblage of clinopyroxene, amphibole, and plagioclase equilibrated at 1.3 GPa and 720°C. Isochemical phase equilibrium modelling of a symplectite of clinopyroxene, plagioclase, and amphibole after omphacite, combined with the mineral composition, yields a P–T range at 1.0–1. 6 GPa, 680–1,000°C. The assemblage of amphibole and plagioclase is estimated to reach equilibrium at 717–732°C, calculated by amphibole–plagioclase thermometry for the former melt‐bearing domain and symplectite respectively. The results of this study demonstrate that partial melt formed in the UHP eclogite through breakdown of an epidote‐group mineral with minor involvement of phengite during exhumation from peak pressure; melt was subsequently crystallized on the cooling path.     

Formation of corundum megacrysts during H<Subscript>2</Subscript>O-saturated incongruent melting of feldspar: P–T pseudosection-based modelling from the Skattøra migmatite complex,North Norwegian Caledonides

Corundum megacryst-bearing rocks associated with the high-pressure migmatites of the Skattøra migmatite complex (SMC) belonging to the Nakkedal Nappe Complex, North Norwegian Caledonides, display a classical example of incongruent melting of plagioclase under water-saturated conditions. Petrography and micro-textures suggest that several centimetre long corundum megacrysts formed from the silicate melt along with amphibole (pargasite) and plagioclase (X_An ~ 0.47). The corundum-bearing leucosomes are rich in biotite compared to the other mafic units of SMC. Locally, margarite occurs in coronas around corundum megacrysts. Geochemically, the corundum-bearing rocks are enriched in Al, K, Rb and Ba and depleted in Fe, Mg and Ca compared to the leucogabbroic host rock. A P–T pseudosection of the leucogabbro indicates that feldspar breakdown and corundum formation occurred at temperatures >850 °C and pressure >1.2 GPa. The calculated equilibrium P–T of the corundum-bearing rock corresponds to 750–825 °C and 0.9–1.1 GPa. The P–T pseudosection of margarite indicates that margarite formed after cooling and decompression to P–T conditions corresponding to 600 °C at 0.5 GPa. Based on geochemical and mineral chemical analysis coupled with thermodynamic modelling, we suggest that formation of corundum occurred as a result of high-pressure incongruent melting of plagioclase in the presence of a K-, Rb- and Ba-rich external fluid. It is also suggested that the external fluid transported out portions of Ca, Fe and Mg, resulting in an increase of the peraluminousity of the melt and promoting further growth of corundum.     

Volcanic red-bed copper mineralisation related to submarine basalt alteration,Mont Alexandre,Quebec Appalachians,Canada

Two types of native copper occur in Upper Silurian basaltic rocks in the Mont Alexandre area, Quebec Appalachians: (1) type 1 forms micrometric inclusions in plagioclase and is possibly magmatic in origin, whereas (2) type 2 occurs as coarse-grained patches rimmed by cuprite in altered porphyritic basalt. Type 1 has higher contents of sulphur (2,000–20,263 ppm) and arsenic (146–6,017 ppm), and a broader range of silver abundances (<65–2,186 ppm Ag) than type 2 (149–1,288 ppm S, <90–146 As, <65–928 ppm Ag). No mineral inclusions of sulphide or arsenide in native copper were observed at the electron-microprobe scale. Primary igneous fabrics are preserved, but the basaltic flows are pervasively oxidised and plagioclase is albitised. Chlorite replaces plagioclase and forms interstitial aggregates in the groundmass and has Fe/(Fe+Mg) ratios ranging from 0.29 to 0.36 with calculated temperatures between 155°C and 182°C. Copper sulphides in vacuoles and veinlets are associated with malachite, fibro-radiating albite and yarrowite (Cu₉S₈ with up to 0.3 wt% Ag). Bulk-rock concentrations of thallium and lithium range from 70 to 310 ppb and 10 to 22 ppm, respectively, and thallium is positively correlated with Fe₂O₃. Such concentrations of thallium and lithium are typical of spilitisation during heated seawater–basalt interaction. Spilitisation is consistent with the regional geological setting of deepwater-facies sedimentation, but is different from current models for volcanic red-bed copper, which indicate subaerial oxidation of volcanic flows. The volcanic red-bed copper model should be re-examined to account for native copper mineralisation in basalts altered by warm seawater.     

Time–temperature evolution of microtextures and contained fluids in a plutonic alkali feldspar during heating

Microtextural changes brought about by heating alkali feldspar crystals from the Shap granite, northern England, at atmospheric pressure, have been studied using transmission and scanning electron microscopy. A typical unheated phenocryst from Shap is composed of about 70 vol% of tweed orthoclase with strain-controlled coherent or semicoherent micro- and crypto-perthitic albite lamellae, with maximum lamellar thicknesses <1 μm. Semicoherent lamellae are encircled by nanotunnel loops in two orientations and cut by pull-apart cracks. The average bulk composition of this microtexture is Ab_27.6Or_71.8An_0.6. The remaining 30 vol% is deuterically coarsened, microporous patch and vein perthite composed of incoherent subgrains of oligoclase, albite and irregular microcline. The largest subgrains are ~3 μm in diameter. Heating times in the laboratory were 12 to 6,792 h and T from 300°C into the melting interval at 1,100°C. Most samples were annealed at constant T but two were heated to simulate an ⁴⁰Ar/³⁹Ar step-heating schedule. Homogenisation of strain-controlled lamellae by Na↔K inter-diffusion was rapid, so that in all run products at >700°C, and after >48 h at 700°C, all such regions were essentially compositionally homogeneous, as indicated by X-ray analyses at fine scale in the transmission electron microscope. Changes in lamellar thickness with time at different T point to an activation energy of ~350 kJmol⁻¹. A lamella which homogenised after 6,800 h at 600°C, therefore, would have required only 0.6 s to do so in the melting interval at 1,100°C. Subgrains in patch perthite homogenised more slowly than coherent lamellae and chemical gradients in patches persisted for >5,000 h at 700°C. Homogenisation T is in agreement with experimentally determined solvi for coherent ordered intergrowths, when a 50–100°C increase in T for An₁ is applied. Homogenisation of lamellae appears to proceed in an unexpected manner: two smooth interfaces, microstructurally sharp, advance from the original interfaces toward the mid-line of each twinned, semicoherent lamella. In places, the homogenisation interfaces have shapes reflecting the local arrangements of nanotunnels or pull-aparts. Analyses confirm that the change in alkali composition is also relatively sharp at these interfaces. Si–Al disordering is far slower than alkali homogenisation so that tweed texture in orthoclase, tartan twinning in irregular microcline, and Albite twins in albite lamellae and patches persisted in all our experiments, including 5,478 h at 700°C, 148 h at 1,000°C and 5 h at 1,100°C, even though the ensemble in each case was chemically homogeneous. Nanotunnels and pull-aparts were modified after only 50 min at 500°C following the simulated ⁴⁰Ar/³⁹Ar step-heating schedule. New features called ‘slots’ developed away from albite lamellae, often with planar traces linking slots to the closest lamella. Slot arrays were often aligned along ghost-like regions of diffraction contrast which may mark the original edges of lamellae. We suggest that the slot arrays result from healing of pull-aparts containing fluid. At 700°C and above, the dominant defects were subspherical ‘bubbles’, which evolved from slots or from regions of deuteric coarsening. The small degree of partial melting observed after 5 h at 1,100°C was often in the vicinity of bubbles. Larger micropores, which formed at subgrain boundaries in patch perthite during deuteric coarsening, retain their shape up to the melting point, as do the subgrain boundaries themselves. It is clear that modification of defects providing potential fast pathways for diffusion in granitic alkali feldspars begins below 500°C and that defect character progressively changes up to, and beyond, the onset of melting.     

P-T-X-controlled element transport through granulite-facies ternary feldspar from Lofoten,Norway

Fluid transport on the grain-scale controls many rock properties and governs chemical exchange. Charnockites from Lofoten indicate fluid penetration into ternary alkali feldspars controlled by their microtextures. In a process of fluid infiltration at granulite-facies conditions (∼600°C and 8–11 kbar), tiny pyroxenes enclosed in alkali feldspar reacted to amphiboles, which are always spatially connected to perthitic albite. Investigation of these microtextures by TEM imaging of Focused Ion Beam (FIB) prepared foils revealed that pyroxenes in contact with albite lamellae show dissolution features. An amorphous Fe- and Cl-bearing material interpreted to be a residuum of the percolating fluid was found within albite lamellae. Textures and mineral compositions indicate that a Cl-rich aqueous fluid attacked the lamellae, which then provided pathways for further fluid flow. A correspondence was found between feldspar compositions, their microtexture and their degree of alteration as a result of their permeability for fluids at specific temperatures. Hence, in addition to pressure and temperature, small variations of feldspar composition can strongly influence the fluid permeability of feldspathic rocks under lower crustal conditions.     

The replacement of plagioclase feldspars by albite: observations from hydrothermal experiments

Oligoclase and labradorite crystals have been experimentally replaced by albite in an aqueous sodium silicate solution at 600°C and 2 kbars. The replacement is pseudomorphic and is characterised by a sharp chemical interface which progresses through the feldspar while preserving the crystallographic orientation. Reaction rims of albite, up to 50 μm thick, can be readily achieved within 14 days. Re-equilibration of plagioclase in an ¹⁸O-enriched sodium- and silica-bearing solution results in oxygen isotope redistribution within the feldspar framework structure. The observed characteristics of the reaction products are similar to naturally albitised plagioclase and are indicative of an interface-coupled dissolution–reprecipitation mechanism. Chemical analyses demonstrate that the albitisation is accompanied by the mobilisation of major, minor and trace elements also including elements such as Al and Ti which are commonly regarded as immobile during hydrothermal alteration. The results contribute to developing our understanding of the close association between large-scale albitisation and secondary ore mineralisation which is common in nature.     

Fluid evolution of rare-element and muscovite granitic pegmatites from central Galicia, NW Spain

Fluid inclusions have been studied in three pegmatite fields in Galicia, NW Iberian Peninsula. Based on microthermometry and Raman spectroscopy, eight fluid systems have been recognized. The first fluid may be considered to be a pegmatitic fluid which is represented by daughter mineral (silicates)-rich aqueous inclusions. These inclusions are primary and formed above 500 °C (dissolution of daughter minerals). During pegmatite crystallization, this fluid evolved to a low-density, volatile-rich aqueous fluid with low salinity (93% H₂O; 5% CO₂; 0.5% CH₄; 0.2% N₂; 1.3% NaCl) at minimum P–T conditions around 3 ± 0.5 kbar and 420 °C. This fluid is related to rare-metal mineralization. The volatile enrichment may be due to mixing of magmatic fluids and fluids equilibrated with the host rock. A drop in pressure from 3 ± 0.5 to 1 kbar at a temperature above 420 °C, which may be due to the transition from predominantly lithostatic to hydrostatic pressure, is recorded by two-phase, water-rich inclusions with a low-density vapour phase (CO₂, CH₄ and N₂). Another inclusion type is represented by two-phase, vapour-rich inclusions with a low-density vapour phase (CO₂, CH₄ and N₂), indicating a last stage of decreasing temperature (360 °C) and pressure (around 0.5 kbar), probably due to progressive exhumation. Finally, volatile (CO₂)-rich aqueous inclusions, aqueous inclusions (H₂O-NaCl) and mixed-salt aqueous inclusions with low Th, are secondary in charac- ter and represent independent episodes of hydrothermal fluid circulation below 310 °C and 0.5 kbar. Received: 14 October 1999 / Accepted: 5 October 1999     

Palaeoproterozoic A-type felsic magmatism in the Khetri Copper Belt, Rajasthan, northwestern India: petrologic and tectonic implications

Summary A number of small Palaeoproterozoic granitoid plutons were emplaced in the Khetri Copper Belt, which is an important Proterozoic metallogenic terrane in the northeastern part of Aravalli mountain range. Contiguous Biharipur and Dabla plutons are located about 15 km southeast of Khetri, close to a 170 km long intracontinental rift zone. The plutons are composed of amphibole-bearing alkali-feldspar granites, comprising microcline-albite granite, albite granite and late-stage microgranite. The albite granite in Biharipur is confined to the margins of the pluton, and shows extensive commingling with the synchronous mafic plutonics. Geochemically, the albite granites are characterised by low K₂O (∼0.5 wt.%) and elevated Na₂O (∼7.0 wt.%) abundances. By contrast, the microcline-albite granite does not show any significant mafic-granite interactions and shows normal concentrations of alkali elements. The granitoids display high concentrations of the rare earth (except Eu) and high field strength elements, high values of Ga/Al (>2.5), agpaitic index and Fe^*-number. These features together with their alkaline metaluminous and ferroan nature classify the rocks as typical A-type within-plate granites. All the granitoid facies display similar REE and incompatible element profiles indicating their cogenetic nature. These granitoids were emplaced in a shallow crustal chamber under relatively low pressures, high temperature (≥850 °C) and relatively oxidising conditions. The oxidised nature, HFSE concentrations and Nd isotope data (ɛNd = −1.3 to −2.9) favour derivation of these granitoid rocks from crustal protoliths. The generation of albite granite is attributed to the replacement of alkali feldspar and plagioclase of the original granite by pure albite as a consequence of pervasive infiltration of a high Na/(Na + K) fluid at the late-magmatic stage. This model may have wider significance for the generation of albite granites/low-K granites or albitites in other areas. The A-type plutonism under consideration seems to be an outcome of ensialic rifting of the Bhilwara aulacogen.     

P–T–t evolution of spinel–cordierite–garnet gneisses from the Sauwald Zone (Southern Bohemian Massif, Upper Austria): is there evidence for two independent late-Variscan low-P/high-T events in the Moldanubian Unit?

The Sauwald Zone, located at the southern rim of the Bohemian Massif in Upper Austria, belongs to the Moldanubian Unit. It exposes uniform biotite + plagioclase ± cordierite paragneisses that formed during the post-collisional high-T/low-P stage of the Variscan orogeny. Rare metapelitic inlayers contain the mineral assemblage garnet + cordierite + green spinel + sillimanite + K-feldspar + plagioclase + biotite + quartz. Mineral chemical and textural data indicate four stages of mineral growth: (1) peak assemblage as inclusions in garnet (stage 1): garnet core + cordierite + green spinel + sillimanite + plagioclase (An_35–65); (2) post-peak assemblages in the matrix (stages 2, 3): cordierite + spinel (brown-green and brown) ± sillimanite ± garnet rim + plagioclase (An_10–45); and (3) late-stage growth of fibrolite, muscovite and albite (An_0–15) during stage 4. Calculation of the P–T conditions of the peak assemblage (stage 1) yields 750–840°C, 0.29–0.53 GPa and for the stage 2 matrix assemblage garnet + cordierite + green spinel + sillimanite + plagioclase 620–730°C, 0.27–0.36 GPa. The observed phase relations indicate a clockwise P–T path, which terminates below 0.38 GPa. The P–T evolution of the Sauwald Zone and the Monotonous Unit are very similar, however, monazite ages of the former are younger (321 ± 9 Ma vs. 334 ± 1 Ma). This indicates that high-T/low-P metamorphism in the Sauwald Zone was either of longer duration or there were two independent phases of late-Variscan low-P/high-T metamorphism in the Moldanubian Unit.     

Enigmatic diamonds in Archean calc-alkaline lamprophyres of Wawa, southern Ontario, Canada

A suite of 80 macrodiamonds recovered from volcaniclastic breccia of Wawa (southern Ontario) was characterized on the basis of morphology, nitrogen content and aggregation, cathodoluminescence (CL), and mineral inclusions. The host calc-alkaline lamprophyric breccias were emplaced at 2.68–2.74 Ga, contemporaneously with voluminous bimodal volcanism of the Michipicoten greenstone belt. The studied suite of diamonds differs from the vast majority of diamond suites found worldwide. First, the suite is hosted by calc-alkaline lamprophyric volcanics rather than by kimberlite or lamproite. Second, the host volcanic rock is amongst the oldest known diamondiferous rocks on Earth, and has experienced regional metamorphism and deformation. Finally, most diamonds show yellow-orange-red CL and contain mineral inclusions not in equilibrium with each other or their host diamond. The majority of the diamonds in the Wawa suite are colorless, weakly resorbed, octahedral single crystals and aggregates. The diamonds contain 0–740 ppm N and show two modes of N aggregation at 0–30 and 60–95% B-centers suggesting mantle storage at 1,100–1,170°C. Cathodoluminescence and FTIR spectroscopy shows that emission peaks present in orange CL stones do not likely result from irradiation or single substitutional N, in contrast to other diamonds with red CL. The diamonds contain primary inclusions of olivine (Fo₉₂ and Fo₈₉), omphacite, orthopyroxene (En₉₃), pentlandite, albite, and An-rich plagioclase. These peridotitic and eclogitic minerals are commonly found within single diamonds in a mixed paragenesis which also combines shallow and deep phases. This apparent disequilibrium can be explained by effective small-scale mixing of subducted oceanic crust and mantle rocks in fast “cold” plumes ascending from the top of the slabs in convergent margins. Alternatively, the diamonds could have formed in the pre-2.7–2.9 Ga cratonic mantle and experienced subsequent alteration of syngenetic inclusions related to host magmatism and ensuing metamorphism. Neither orogenic nor cratonic model of the diamond origin fully explains all of the observed characteristics of the diamonds and their host rocks. Electronic Supplementary Material Supplementary material is available for this article at and is accessible for authorized users.     

Fluid characteristics of retrogressed eclogites and mafic granulites from the Cambrian Gondwana suture zone in southern India

Eclogite-facies rocks and high-pressure granulites provide windows to the deeper parts of subduction zones and the root of mountain chains, carrying potential records of fluids associated with subduction-accretion-collision tectonics. Here, we report petrological and fluid inclusion data on retrogressed eclogite and high-pressure granulite samples from Sittampundi, Kanji Malai and Perundarai in southern India. These rocks occur within the trace of the Cambrian collisional suture which marks the final phase of amalgamation of the Gondwana supercontinent. The garnet–clinopyroxene assemblage in the eclogites preserves relict omphacite, whereas the high-pressure granulites are characterized by an assemblage of garnet and clinopyroxene in the absence of omphacite and with minor plagioclase, orthopyroxene, and quartz. Phase relations computed for the eclogite assemblage yield peak P–T conditions of 19 kbar and 1,010°C. The mafic granulites also preserve the memory of high to ultrahigh-temperature metamorphism followed by an isothermal decompression. Systematic fluid inclusion optical, microthermometric and laser Raman spectroscopic studies were conducted in garnet and plagioclase from the eclogite–high pressure granulite suite. The results suggest that the early fluids were a mixture of CO₂, CH₄ and N₂ probably derived from decarbonation and devolatilization reactions in a subduction setting during the prograde stage. The later generation inclusions, which constitute the dominant category in all the samples studied, are characterized by a near-pure CO₂ composition with moderate to high densities (up to 1.154 g/cm³). The highest density fluid inclusions recorded in this study occur within the mafic granulites from Sittampundi (0.968–1.154 g/cm³) and Kanji Malai (1.092–1.116 g/cm³). In some cases, carbonate minerals such as dolomite and calcite are associated with the CO₂-rich fluid inclusions. The composition and densities of the later generation fluids closely match with those of the CO₂-bearing fluid inclusions reported from ultrahigh-temperature granulites occurring proximal to the eclogite–high pressure granulite suite within this suture zone, and suggest a common tectonic link for the fluid regime. We evaluate the fluid characteristics associated with convergent plate margin processes and propose that the early aqueous fluids probably associated with the eclogites were consumed during the formation of the retrograde hydrous mineral assemblages, whereas the fluid regime of the high-pressure and ultrahigh-temperature granulites was mostly CO₂-dominated. The tectonic setting of the rocks along a collisional suture marking the trace along which crustal blocks were welded through subduction–collision process is in favor of a model involving the derivation of CO₂ from sub-lithospheric sources such as a carbonated tectosphere invaded by hot asthenosphere, or underplated mafic magmas.     

K-feldspar–quartz and K-feldspar–plagioclase phase boundary interactions in garnet–orthopyroxene gneiss's from the Val Strona di Omegna, Ivrea–Verbano Zone, northern Italy

A detailed study based on textural observations combined with microanalysis [back scattered electron imaging (BSE) and electron microprobe analysis (EMPA)] and microstructural data transmission electron microscopy (TEM) has been made of K-feldspar micro-veins along quartz–plagioclase phase and plagioclase–plagioclase grain boundaries in granulite facies, orthopyroxene–garnet-bearing gneiss's (700–825 °C, 6–8 kbar) from the Val Strona di Omegna, Ivrea–Verbano Zone, northern Italy. The K-feldspar micro-veins are commonly associated with quartz and plagioclase and are not found in quartz absent regions of the thin section. This association appears to represent a localised reaction texture resulting from a common high grade dehydration reaction, namely: amphibole + quartz = orthopyroxene + clinopyroxene + plagioclase + K-feldspar + H₂O, which occurred during the granulite facies metamorphism of these rocks. There are a number of lines of evidence for this. These include abundant Ti-rich biotite, which was apparently stable during granulite facies metamorphism, and total lack of amphibole, which apparently was not. Disorder between Al and Si in the K-feldspar indicates crystallisation at temperatures >500 °C. Myrmekite and albitic rim intergrowths in the K-feldspar along the K-feldspar–plagioclase interface could only have formed at temperatures >500–600 °C. Symplectic intergrowths of albite and Ca-rich plagioclase between these albitic rim intergrowths and plagioclase suggest a high temperature grain boundary reaction, which most likely occurred at the start of decompression in conjunction with a fluid phase. Relatively high dislocation densities (>2 × 10⁹ to 3 × 10⁹/cm²) in the K-feldspar suggest plastic deformation at temperatures >500 °C. We propose that this plastic deformation is linked with the extensional tectonic environment present during the mafic underplating event responsible for the granulite facies metamorphism in these rocks. Lastly, apparently active garnet grain rims associated with side inclusions of K-feldspar and quartz and an exterior K-feldspar micro-vein indicate equilibrium temperatures within 20–30 °C of the peak metamorphic temperatures estimated for the sample (770 °C). Contact between these K-feldspar micro-veins and Fe-Mg silicate minerals, such as garnet, orthopyroxene, clinopyroxene or biotite along the interface, is observed to be very clean with no signs of melt textures or alteration to sheet silicates. This lends support to the idea that these micro-veins did not originate from a melt and, if fluid induced, that the water activity of these fluids must have been relatively low. All of these lines of evidence point to a high grade origin for the K-feldspar micro-veins and support the hypothesis that they formed during the granulite facies metamorphism of the metabasite layers in an extensional tectonic environment as the consequence of localised dehydration reactions involving the breakdown of amphibole in the presence of quartz to orthopyroxene, clinopyroxene, plagioclase, K-feldspar and H₂O. It is proposed that the dehydration of the metabasite layers to an orthopyroxene–garnet-bearing gneiss over a 4-km traverse in the upper Val Strona during granulite facies metamorphism was a metasomatic event initiated by the presence of a high-grade, low H₂O activity fluid (most likely a NaCl–KCl supercritical brine), related to the magmatic underplating event responsible for the Mafic Formation; and that this dehydration event did not involve partial melting. Received: 15 February 2000 / Accepted: 26 June 2000     

Cathodoluminescence,fluid inclusion and stable C–O isotope study of tectonic breccias from thrusting plane of a thin-skinned calcareous nappe

Basal hydraulic breccias of alpine thin-skinned Muráň nappe were investigated by means of cathodoluminescence petrography, stable isotope geochemistry and fluid inclusions analysis. Our study reveals an unusual dynamic fluid regime along basal thrust plane during final episode of the nappe emplacement over its metamorphic substratum. Basal thrusting fluids enriched in ¹⁸O, silica, alumina, alkalies and phosphates were generated in the underlying metamorphosed basement at epizonal conditions corresponding to the temperatures of 400–450°C. The fluids fluxed the tectonized nappe base, leached evaporite-bearing formations in hangingwall, whereby becoming oversaturated with sulphates and chlorides. The fluids further modified their composition by dedolomitization and isotopic exchange with the host carbonatic cataclasites. Newly formed mineral assemblage of quartz, phlogopite, albite, potassium feldspar, apatite, dravite tourmaline and anhydrite precipitated from these fluids on cooling down to 180–200°C. Finally, the cataclastic mush was cemented by calcite at ambient anchizonal conditions. Recurrent fluid injections as described above probably enhanced the final motion of the Muráň nappe.     

Constraints from monazite and xenotime growth modelling in the MnCKFMASH‐PYCe system on the P–T path of a metapelite from Shillong‐Meghalaya Plateau: implications for the Indian shield assembly

The Palaeo‐Mesoproterozoic metapelite granulites from northern Garo Hills, western Shillong‐Meghalaya Gneissic Complex (SMGC), northeast India, consist of resorbed garnet, cordierite and K‐feldspar porphyroblasts in a matrix comprising shape‐preferred aggregates of biotite±sillimanite+quartz that define the penetrative gneissic fabric. An earlier assemblage including biotite and sillimanite occurs as inclusions within the garnet and cordierite porphyroblasts. Staurolite within cordierite in samples without matrix sillimanite is interpreted to have formed by a reaction between the sillimanite inclusion and the host cordierite during retrogression. Accessory monazite occurs as inclusions within garnet as well as in the matrix, whereas accessory xenotime occurs only in the matrix. The monazite inclusions in garnet contain higher Ca, and lower Y and Th/U than the matrix monazite outside resorbed garnet rims. On the other hand, matrix monazite away from garnet contains low Ca and Y, and shows very high Th/U ratios. The low Th/U ratios (<10) of the Y‐poor garnet‐hosted monazite indicate subsolidus formation during an early stage of prograde metamorphism. A calculated P–T pseudosection in the MnCKFMASH‐PYCe system indicates that the garnet‐hosted monazite formed at <3 kbar/600 °C (Stage A). These P–T estimates extend backward the previously inferred prograde P–T path from peak anatectic conditions of 7–8 kbar/850 °C based on major mineral equilibria. Furthermore, the calculated P–T pseudosections indicate that cordierite–staurolite equilibrated at ~5.5 kbar/630 °C during retrograde metamorphism. Thus, the P–T path was counterclockwise. The Y‐rich matrix monazite outside garnet rims formed between ~3.2 kbar/650 °C and ~5 kbar/775 °C (Stage B) during prograde metamorphism. If the effect of bulk composition change due to open system behaviour during anatexis is considered, the P–T conditions may be lower for Stage A (<2 kbar/525 °C) and Stage B (~3 kbar/600 °C to ~3.5 kbar/660 °C). Prograde garnet growth occurred over the entire temperature range (550–850 °C), and Stage‐B monazite was perhaps initially entrapped in garnet. During post‐peak cooling, the Stage‐B monazite grains were released in the matrix by garnet dissolution. Furthermore, new matrix monazite (low Y and very high Th/U ≤80, ~8 kbar/850–800 °C, Stage C), some monazite outside garnet rims (high Y and intermediate Th/U ≤30, ~8 kbar/800–785 °C, Stage D), and matrix xenotime (<785 °C) formed through post‐peak crystallization of melt. Regardless of textural setting, all monazite populations show identical chemical ages (1630–1578 Ma, ±43 Ma). The lithological association (metapelite and mafic granulites), and metamorphic age and P–T path of the northern Garo Hills metapelites and those from the southern domain of the Central Indian Tectonic Zone (CITZ) are similar. The SMGC was initially aligned with the southern parts of CITZ and Chotanagpur Gneissic Complex of central/eastern India in an ENE direction, but was displaced ~350 km northward by sinistral movement along the north‐trending Eastern Indian Tectonic Zone in Neoproterozoic. The southern CITZ metapelites supposedly originated in a back‐arc associated with subducting oceanic lithosphere below the Southern Indian Block at c. 1.6 Ga during the initial stage of Indian shield assembly. It is inferred that the SMGC metapelites may also have originated contemporaneously with the southern CITZ metapelites in a similar back‐arc setting.     

Late‐stage orogenic loading revealed by contact metamorphism in the northern Appalachians,New York

Pelitic schists from contact aureoles surrounding mafic–ultramafic plutons in Westchester County, NY record a high‐P (~0.8 GPa) high‐T (~790 °C) contact overprint on a Taconic regional metamorphic assemblage (~0.5 GPa). The contact metamorphic assemblage of a pelitic sample in the innermost aureole of the Croton Falls pluton, a small (<10 km²) gabbroic body, consists of quartz–plagioclase–biotite–garnet–sillimanite–ilmenite–graphite–Zn‐rich Al‐spinel. Both K‐feldspar and muscovite are absent, and abundant biotite, plagioclase, sillimanite, quartz and ilmenite inclusions are found within subhedral garnet crystals. Unusually low bulk‐rock Na and K contents imply depletion of alkalic components and silica through anatexis and melt extraction during contact heating relative to typical metapelites outside the aureole. Thermobarometry on nearby samples lacking a contact overprint yields 620–640 °C and 0.5–0.6 GPa. In the aureole sample, WDS X‐ray chemical maps show distinct Ca‐enriched rims on both garnet and matrix plagioclase. Furthermore, biotite inclusions within garnet have significantly higher Mg concentration than matrix biotite. Thermobarometry using GASP and garnet–biotite Mg–Fe exchange equilibria on inclusions and adjacent garnet host interior to the high‐Ca rim zone yield ~0.5 ± 0.1 GPa and ~620 ± 50 °C. Pairs in the modified garnet rim zone yield ~0.9 ± 0.1 GPa and ~790 ± 50 °C. Thermocalc average P–T calculations yield similar results for core (~0.5 ± ~0.1 GPa, ~640 ± ~80 °C) and rim (~0.9 ± ~0.1 GPa, ~800 ± ~90 °C) equilibria. The core assemblages are interpreted to record the P–T conditions of peak metamorphism during the Taconic regional event whereas the rim compositions and matrix assemblages are interpreted to record the P–T conditions during the contact event. The high pressures deduced for this later event are interpreted to reflect loading due to the emplacement of Taconic allochthons in the northern Appalachians during the waning stages of regional metamorphism (after c. 465 Ma) and before contact metamorphism (c. 435 Ma). In the absence of contact metamorphism‐induced recrystallization, it is likely that this regional‐scale loading would remain cryptic or unrecorded.     

ON THE REACTION OF OLIGOCLASE WITH WATER UNDER CONDITIONS OF HIGH TEMPERATURE AND PRESSURE

Feldspar group minerals reacting with water at depth determine, by their reaction with environment, the character of newly formed minerals. Although plagioclase is the most abundant member of this group experimental data are very limited on the nature of its reactions under high pressure and temperature conditions. The author experimented on acid plagioclase with analytical data and physical constants corresponding to those of oligoclase. The reaction between oligoclase and water was studied under various pressures and temperatures, using a diffusion autoclave (previously described by the author [1]). Silicon, sodium, and aluminum in significant amounts went into solution; and, smaller amounts of calcium and potassium were observed. With increased temperature, larger amounts of material constituting oligoclase went into solution: The maximum occurred at 350 to 400° C; and, a marked decrease, at 500 to 600° C. Quantitative ratios of material in the condensate were found to correspond to albite indices. Increased pressure does not alter this behavior, there is only increased passage of separate components of the mineral into solution. At 350°, newly formed material was not observed microscopically; at higher temperatures, kaolinite and chalcedony appeared at sucessively higher temperatures. Experimentation by Morey and Chen on albite indicate that transfer of the albite component of oligoclase into solution is predominant. By comparison of its stability with that of two other minerals, albite is the most reactive with water. At 350° Centigrade and under pressure of 350 kilograms per square centimeter, the transfer into solution (in milligrams per liter) is for albite, 318; for microcline, 268; and, for oligoclase, 220. Labradorite was studied under analogous conditions; in that the transfer of labradorite predominates over that of the anorthite molecule, its behavior corresponds to albite. It was found that basic plagioclase shows less stability than is evident from microscopic examination of plagioclase in rocks. Data from these and previous experiments indicate possible types of solutions that can form within intragranular spaces in rocks by reaction between acid plagioclase and water. It is evident from the data that leaching of the albite component predominates by variation in composition of the solution throughout a wide range of temperature and pressure conditions. --D. D.Fisher     

Tectonic implications of garnet-bearing mantle xenoliths exhumed by Quaternary magmatism in the Hangay dome, central Mongolia

Garnet-bearing mantle xenoliths have been recovered from Quaternary alkali basalts, both within and peripheral to the Hangay dome of central Mongolia. Microfabric analysis and thermobaromery, combining empirical thermobarometers and the self-consistent dataset of THERMOCALC, indicate that garnet websterites from the Shavaryn-Tsaram volcanic centre at the dome core were formed in the spinel-lherzolite upper mantle at pressures of 17–18 kbars and temperatures of 1,070–1,090°C, whereas garnet lherzolites were derived from greater depths (18–20 kbars). Garnet lherzolites from the Baga Togo Uul vents near the dome edge were formed at 18–22 kbars under significantly cooler conditions (960–1,000°C). These xenoliths reveal reaction coronas of (1) orthopyroxene, clinopyroxene, plagioclase and spinel mantling garnets; (2) spongy rims of olivine replacing orthopyroxene and (3) low-Na, low-Al clinopyroxene replacing primary clinopyroxene. Trace-element abundances indicate that clinopyroxene from these coronas is in chemical equilibrium with the host magma. The thermobarometric and textural data suggest that lherzolite xenoliths from both sites were derived from depths of 60–70 km and entrained in magma at 1,200–1,300°C. The average rate of ascent, as determined by olivine zoning, lies in the range 0.2–0.3 m s⁻¹. The contrast in thermal profiles of the upper mantle between the two sites is consistent with a mantle plume beneath the Hangay dome with elevated thermal conditions beneath the core of the dome being comparable to estimates of the Pleistocene geotherm beneath the Baikal rift.     

Petrologic and experimental evidence for the movement and heating of the pre-eruptive Minoan rhyodacite (Santorini, Greece)

Hydrothermal experiments combined with petrologic observations form the basis for a new two-stage model for the evolution of the pre-eruption Minoan magma chamber at Santorini, Greece. Ninety-nine percent of the erupted volume is two-pyroxene, rhyodacitic magma that had been stored at a temperature of ∼885 °C, based on magnetite-ilmenite and QUILF geothermometry. The rest of the volume is basaltic to andesitic magma, which occurs as <10 cm scoria clasts and as small inclusions in rhyodacite pumices. Petrologic observations show that these magmas mixed at different scales and at different times (i.e., multiple batches of mafic magma). Hydrothermal experiments were carried out on samples of rhyodacite and a mafic scoria in order to determine magma storage conditions and the mixing history of the two magmas. At 885 °C, the rhyodacite must have been stored at water-saturated pressures of ∼50 MPa, based on its phase assemblage, matrix-glass composition, and crystal content. However, glass inclusions inside rhyodacitic plagioclase phenocrysts contain more than 6 wt% H₂O, indicating they formed at pressures >200 MPa. In addition, the composition of the plagioclase hosts (An_{56 ± 6}) of the inclusions require temperatures of 825 ± 25 °C at pressures >200 MPa. This demonstrates that the Minoan rhyodacitic magma underwent a two-stage evolution, first crystallizing at ∼825^∘C and >200 MPa, and then rinsing to a shallow ∼50 MPa storage region with a concomitant rise in temperature to ∼885 °C. We suggest that the episodic intrusion of mafic magmas provided the necessary heat and perhaps contributed to the ascent of the magma to shallow crustal depths where it reequilibrated before the cataclysmic eruption. Phase equilibria suggest that much of the heating of the rhyodacite occurred in the shallow storage region. Thermal budget calculations suggest that the rhyodacite magma could have been heated by intrusions of basalt rising at reasonable upwelling rates and injected into the storage zone over several hundred years. Preservation of amphibole in the mafic scoria indicate that injection of mafic magma continued up until days before the cataclysmic eruption, perhaps triggering the event. Received: 30 September 1997 / Accepted: 5 October 1998     

Mantled feldspars from the Golden Horn batholith,Washington

Mantled feldspars that formed by resorption, development of skeletal plagioclase crystals, and filling with alkali feldspar are common in the Golden Horn batholith, Washington. Subhedral plagioclase mantles have weak normal zoning from An₁₇ to An₁₀. Plagioclase zoning and twinning are crosscut by resorption channels. Resorption cavities and channels are coated with albite (An₁₀). Anhedral, perthitic orthoclase within the plagioclase is optically continuous with orthoclase in channels and on the mantle exterior.This texture resulted from resorption of calcic cores of plagioclase as pressure decreased when water-undersaturated granite magma intruded to a shallow crustal level. At shallow level, only alkali feldspar and quartz crystallized and were available to fill the skeletal plagioclase.