Contrasting mineral parageneses in high-temperature calc-silicate granulites: examples from the Eastern Ghats, India

Abstract Three types of mineral associations are described from calc-silicate granulites from the Eastern Ghats, India, where geothermobarometry in associated rocks suggests extremely high P–T conditions of metamorphism ( c . 9 ± 1 kbar, 950° C). These mineral associations are: (i) calcite + quartz + scapolite + plagioclase, (ii) calcite + scapolite + wollastonite + porphyroblastic garnet + coronal garnet and (iii) calcite + quartz + wollastonite + scapolite + porphyroblastic garnet + coronal garnet, all coexisting with K-feldspar, titanite and clinopyroxene. The first two associations evolved through nearly isobaric cooling retrograde paths, whereas the third evolved through a nearly isothermal decompression path followed by an isobaric cooling retrograde path. Textural and compositional characteristics suggest the following mineral reactions in the calc-silicate granulites: calcite + quartz = wollastonite + CO₂, calcite + plagioclase = scapolite, calcite + scapolite + wollastonite = porphyroblastic garnet ± quartz + CO₂, CaTs + wollastonite = coronal garnet (association ii) and wollastonite + scapolite = coronal garnet (association iii) + quartz + CO₂. Andradite content in garnet was buffered by the redox equilibria wollastonite + hedenbergite + O₂= andradite + quartz (association iii) and wollastonite + andradite + CaTs + scapolite = hedenbergite + calcite + grossular + O₂ (association ii). The contrasting mineral parageneses have been ascribed to interplay of variables such as X _CO2, f _O2, f _HCl in the fluid, bulk Na content and the nature of the retrograde P–T–X _CO2 paths through which the rocks evolved.     

The muscovite-melt bathograd and low-P isograd suites in north-central Wopmay Orogen, Northwest Territories, Canada

In north-central Wopmay Orogen, syntectonic low-P(Buchan-type) suites of mineral isograds outline regional metamorphic temperature culminations that are associated, at the higher structural levels, with emplacement of early Proterozoic plutons in the west part of a deformed and eastward transported continental margin prism. The mapped isograds mark the first occurrence of biotite, staurolite, andalusite, sillimanite, sillimanite-K feldspar and K feldspar-plagioclase-quartz ± muscovite (granitic) pods in metapelites, with increasing proximity to the plutons.
Microprobe analyses and field observations have resulted in the formulation of reactions for the 'ideal'pelitic system K₂O-Na₂O-FeO-MgO-Al₂O₃-SiO₂-H₂O-Al₂O₃-SiO₂-H₂O, to account for the various mineral assemblages of each metamorphic zone. A P-T petrogenetic grid showing erosion surface P-T curves for the northern Wopmay Orogen pelites, compiled on the basis of the mapped isograds and the inferred reaction(s) for each metamorphic zone, documents a variation in exposed metamorphic pressure ranging between 2 and 4 kbar.
The configuration of a new bathograd, based on the invariant model reaction sillimanite + K feldspar + plagioclase + biotite + quartz + vapor ± muscovite + liquid and interpolated across three metamorphic suites, is consistent with a major regional structure culmination and with independently determined pressures obtained from anorthite-grossular-quartz-Al₂SiO₅ geobarometry. The positive correlation between the configuration of the bathograd and the structural and pressure culmination points to the pressure-dependence of anatectic-granitic-pod mineral associations.     

Petrology of Fe-Mg-carpholite-bearing metasediments from NE Oman

Abstract Fe-Mg carpholite occurs in metasediments of tectonically disrupted basement, shelf and foreland basin units that structurally underlie the Semail ophiolite in NE Oman. In the lower grade, structurally higher units, Fe-rich carpholite coexists with paragonite, quartz, illite, kaolinite and chlorite, whereas in deeper units, Fe-Mg carpholite occurs with pyrophyllite, sudoite, phengite and/or chloritoid. Mineral compositions in these units indicate that chlorite is more magnesian than coexisting Fe-Mg carpholite at low temperatures and pressures but, at higher metamorphic grades, X_Mg decreases in the order sudoite > carpholite > chlorite > chloritoid. This suggests a reversal in Fe-Mg partitioning between Fe-Mg carpholite and chlorite at temperatures below or close to those of the breakdown of kaolinite + quartz to pyrophyllite and at X_Mg= 0.35.
Phase relations and mineral equilibria indicate that the P-T conditions of formation of the Fe-Mg-carpholite-bearing rocks of NE Oman range from 280–315° C, 3–6 kbar for the structurally highest units to 325–440° C, 6–9.5 kbar for the deepest units, indicating a systematic down-section increase in metamorphic grade. Textural relations in these rocks, interpreted in the context of pertinent equilibria, are consistent with the clockwise P-T paths previously constrained for these units from petrological studies of interlayered isofacial mafic rocks.     

浙西南八都杂岩早中生代泥质麻粒岩变质作用及构造意义

遂昌-大柘泥质麻粒岩出露于华夏地块东北部的浙西南八都杂岩中,该岩石保留了典型的减压反应结构.但其变质演化特点、变质作用时代及构造意义目前尚不明确.通过系统的岩相学、矿物化学和同位素年代学分析,结果表明遂昌-大柘泥质麻粒岩记录了4个阶段的变质矿物组合,其中早期进变质阶段M₁的矿物组合为石榴石+黑云母+石英;压力峰期变质阶段M₂的矿物组合为石榴石+铝绿泥石+金红石+蓝晶石+刚玉+黑云母+石英±十字石,该矿物组合可能预示着岩石曾经历了超高压变质作用过程;峰期变质阶段M₃的矿物组合为石榴石+黑云母+夕线石+石英±钾长石±斜长石±钛铁矿;峰后近等温降压M_4-1阶段的矿物组合为石榴石+黑云母+夕线石+堇青石+石英+钛铁矿±尖晶石±斜长石±钾长石;M_4-2阶段的矿物组合为石榴石+堇青石+夕线石+斜长石+黑云母+石英±钾长石.相平衡模拟结合传统地质温压计限定其峰期变质阶段的温压条件为T=780~810 ℃、P=8.0~9.2 kbar;峰期后近等温降压的M_4-1阶段的温压条件为T=780~860 ℃和P=5.7~6.0 kbar,M_4-2阶段的温压条件为T=~700 ℃和P=~4.4 kbar,具有典型的顺时针近等温减压型P-T轨迹特征.LA-ICP-MS U-Pb定年结果表明其麻粒岩相变质作用时代为233.5~238.9 Ma.变质作用历史说明浙西南地体可能卷入了古特提斯洋域内印支-华南-华北板块之间的俯冲-碰撞过程,并经历了早中生代的麻粒岩相变质作用后快速折返至地表.      

蚌埠隆起区石榴辉石岩变质P-T轨迹的构建

蚌埠隆起区位于华北克拉通东南缘,胶—辽—吉造山带的最南端,主体由五河杂岩组成。前人对该地区的研究主要集中于同位素年代学和变质温压条件研究,其中变质P-T条件研究结果差异较大,以压力变化最为显著,对峰期变质P-T条件缺乏统一认识。本文对蚌埠隆起区石榴辉石岩进行了大量的岩相学、矿物化学成分分析,表明该岩石记录了3期变质作用,其中S_-M1和S_-M2的矿物组合类似为Grt+Cpx+Opx+Amp+Pl+Ilm,S_-M3的矿物组合为Cpx+Amp+Pl+Grt （极边窄带）。结合变质温压条件分析和锆石U-Pb年代学分析,本次主要取得以下几点认识：1）石榴辉石岩WS047-1中记录的3期变质作用,温压条件分别为T_-M1 = 616 ℃～647 ℃、P_-M1 = 1.03～1.08 GPa,T_-M2 = 721 ℃～837 ℃、P_-M2 = 1.11～1.29 GPa和T_-M3 = 531 ℃～607 ℃、P_-M3 = 0.81～0.91 GPa,经历了由较高压力的角闪岩相→中-低麻粒岩相→角闪岩相的变质过程;2）据变质温压条件分析知,蚌埠隆起区具有顺时针的P-T轨迹特征,S_-M1→S_-M2和S_-M2→S_-M3分别为近等压升温和近等压降温的缓慢过程;3）石榴辉石岩锆石U-Pb年代学结果主要分为4组：1 839±13 Ma、1 925±31 Ma、2 041±55 Ma和2 762±14 Ma,其中峰值变质年代为1.93～1.84 Ga;4）结合温压条件和锆石U-Pb年代学分析结果,本文认为蚌埠隆起区的P-T轨迹与弗朗西斯科型俯冲或大陆碰撞环境的P-T轨迹较为类似,其应与1.93～1.84 Ga华北克拉通东、西陆块的碰撞拼合及胶—辽—吉造山带形成时限基本吻合。本次研究为深入理解华北克拉通的构造演化特征和蚌埠隆起区的变质作用及演化,提供了大量可靠的科学资料。     

The (Na–Ca)amphibole–albite–chlorite–epidote–quartz geothermobarometer in the system S–A–F–M–C–N–H2O. 1. An empirical calibration

The proposed geothermobarometer is based on an empirical calibration which takes account of two equilibria involving the tremolite, edenite, pargasite and hastingsite components in amphiboles. It has applications to assemblages found in metabasic rocks of widely different chemical compositions (magnesian to Fe-rich metabasalts), and for metamorphism ranging from lower greenschist to highest amphibolite facies. Knowing the Si_(T1), Al^iv, Al^vi, Fe³⁺, Fe²⁺, Mg, Ca, Na_M4, Na_A and A vacancy in an amphibole, and the Al³⁺ and X _Mg in coexisting epidote and chlorite, it is possible to calculate two values of In K _d for this assemblage. These equilibria involve edenite-tremolite and (pargasite/hastingsite)-tremolite end-members in amphibole (the calculation program is given). For these equilibria, the isopleths (iso-values of K _d) have been calculated for 0.27 < X _Mg < 0.75 and 0 < X _Fe3+= Fe³⁺/(Fe³⁺+ Al^vi) < 0.8. It is then possible to determine pressure and temperature directly when X _Mg, X _Fe3+, In K _d for tremoliteedenite and In K _d for (pargasite/hastingsite)-tremolite are known. Application of this geothermobarometer is limited to Ca-free plagioclase assemblages, and complete P–T paths can be drawn only if all the minerals are considered together. Phase relations at successive stages of crystallization can be constrained by studying the relationships between the coexisting minerals, their zoning and the metamorphic fabrics.     

Plagioclase relations in pelites, central Menderes Massif, Turkey. I. The peristerite gap with coexisting kyanite

Abstract In pelites of the central Menderes Massif, albite and oligoclase with only slight chemical zoning coexist in apparent textural equilibrium in the garnet zone, staurolite zone, and staurolite + kyanite transition zone. The metamorphic temperature range is estimated as approximately 440–550°C (from the Hodges-Spear calibration of the garnet-biotite geo-thermometer), or 440–500°C (Ganguly-Saxena calibration). While oligoclase composition at the peristerite gap changes from An₂₂ to An₁₄, albite also becomes more sodic (An_1,5–An_0.6). The slope of the albite limb is thus the reverse of that reported in other areas, and may not be a true equilibrium feature. Occurrence of kyanite, at temperatures below the crest of the gap, is due to low water activity in the presence of graphite: a H_2o is estimated at approximately 0.1–0.2 from the Na content of muscovite coexisting with albite + kyanite + quartz.     

On the origin of CO2-rich fluid inclusions in migmatites

Abstract Nearly pure CO₂ fluid inclusions are abundant in migmatites although H₂O-rich fluids are predicted from the phase equilibria. Processes which may play a role in this observation include (1) the effects of decompression on melt, (2) generation of a CO₂-bearing volatile phase by the reaction graphite + quartz + biotite + plagioclase = melt + orthopyroxene + CO₂-rich vapour, (3) selective leakage of H₂O from CO₂+ H₂O inclusions when the pressure in the inclusion exceeds the confining pressure during decompression, and (4) enrichment of grain-boundary vapour in CO₂ by subsolidus retrograde hydration reactions.     

Conditions of Archean granulite metamorphism in the Godthab-Fiskenaesset region, southern West Greenland

The Nordlandet peninsula (Akia terrane) and the Tasiusarsuaq terrane in southern West Greenland were metamorphosed to granulite facies at 3.0 and 2.8 Ga respectively. Temperatures of metamorphism are estimated using magnetite + ilmenite, garnet + orthopyroxene, garnet + clinopyroxene and garnet + biotite thermometers. Barometry has been carried out in the two terranes using eight different garnet barometers. A uniform set of activity models for all minerals, including the garnet activity model of Newton et al. (1986), is applied to each barometer in order to permit comparison. Pressure estimates using the different barometers are generally quite consistent (±1.5 kbar). Use of the Newton et al. (1986) garnet activity data results in pressures similar to those obtained using other garnet activity models.
Peak metamorphic conditions on the Nordlandet peninsula are estimated to have been 800 ± 50°C, 7.9 ± 1.0 kbar. Values of log f _O2 are estimated to have been 1.1 to 2.0 above the quartz + magnetite + fayalite buffer from assemblages of magnetite + ilmenite and quartz + magnetite + ferrosilite. Peak metamorphic conditions in the Tasiusarsuaq terrane are estimated to have been 780 ± 50°C, 8.9 ± 1.0 kbar. Estimates of f _H2O and f _CO2 using biotite, amphibile, grossular + anorthite and grossular + scapolite equilibria are low in both terranes. These results suggest that granulite metamorphism was fluid absent in both terranes, and that the metamorphism in the Akia terrane and possibly also in the Tasiusarsuaq terrane was initiated by the injection of large volumes of magma into the lower crust.     

P-T grids for silica-undersaturated granulites in the systems MAS (n+ 4) and FMAS (n+ 3)-tools for the derivation of P-T paths of metamorphism

Abstract Considering the minerals cordierite (Cd), sapphirine (Sa), hypersthene (Hy), garnet (Ga), spinel (Sp), sillimanite (Si) and corundum (Co) in the system FeO-MgO-Al₂O₃-SiO₂ (FMAS), the stable invariant points are [Co], [Ga], [Cd] and [Sa]. Constraints imposed by experimental data for the system MAS indicate that under low P _H2o conditions the invariant points occur at high temperature (> 900° C) and intermediate pressure (7-10 kbar). This temperature is higher than that commonly advocated for granulite facies metamorphism. In granulites Fe-Mg exchange geothermometers may yield temperatures of 100–150° C below peak metamorphic conditions and evidence for peak temperatures is best preserved by relict high-temperature assemblages and by Al-rich cores in orthopyroxene. Application of the FMAS grid to some well-documented granulite occurrences introduces important constraints on their P-T histories. Rocks of different bulk compositions, occurring in close proximity in the field, may record distinct segments of their P-T paths. This applies particularly to rocks with evidence for reaction in the form of coronas, symplectites and zoned minerals. Consideration of curved reaction boundaries and _XMs isopleths may explain apparently contradictory results for the stability of cordierite obtained from low-temperature experiments and thermochemical calculations on the one hand and hightemperature experimental data on the other.     

Bulk composition and mineral parageneses of sapphirine-bearing rocks along a gabbro-lherzolite contact at Finero, Ivrea Zone, N Italy

Sapphirine occurs in a 3-5 m wide zone between amphibole-lherzolite and garnetiferous metagabbro at Finero in the Ivrea Zone, NW Italian Alps. Layers consisting of plag + hb + sa + cpx + opx + sp + gt are interbanded with spinel pyroxenites, which may contain sapphirine replacing spinel. All minerals are very magnesian, with X_Mg between 0.78 and 0.92. Bulk rock analyses suggest that precursors to the sapphirine-bearing rocks were igneous cumulates of plagioclase + olivine + hornblende + spinel. Up to 16wt% CaO does not inhibit sapphirine formation and it is the unusually Mg-rich nature of the host rocks which allows sapphirine development. The early igneous assemblage was replaced by one of cpx + sa + hb +± plag at a pressure of 9 ± 1 kbar and temperatures of 900 ± 50°C. Subsequent rapid uplift caused the instability of gt, gt + hb, hb and sa + cpx to form opx + plag ± sp ± sa symplectites.     

Controls on the first appearance of jadeitic pyroxene, northern Diablo Range, California

A reaction producing jadeitic pyroxene in metagreywackes of the northern Diablo Range has been identified on the basis of mineral distribution, isograd patterns and composition of coexisting minerals. The appearance of jadeitic pyroxene (∼Jd₈₀) is closely followed by the disappearance of pumpellyite, which indicates that pumpellyite plays a major role in the pyroxene-producing reaction. A new projection from hematite, lawsonite, chlorite, quartz and H₂O on to the NaAlO₂-FeO-MgO ternary confirms the role of pumpellyite in pyroxene production and suggests a reaction of the form: 1.00 pumpellyite + 0.31 chlorite + 8.71 albite + 0.70 hematite + 2.00 H₂O = 8.54 jadeite + 0.57 glaucophane + 3.09 lawsonite + 5.26 quartz. Metagreywackes of the northern Diablo Range were metamorphosed under conditions of P _H2O= P _total at 200-300 °C and 7.5-10.0 kbar. Despite the low temperatures attained during metamorphism, the assumption of equilibrium yields results consistent with field observations and phase relations.     

Petrology of pelitic schists in the oligoclase-biotite zone of the Sanbagawa metamorphic terrain, Japan: phase equilibria in the highest grade zone of a high-pressure intermediate type of metamorphic belt

The oligoclase-biotite zone of the Bessi area, central Shikoku is characterized by sodic plagioclase (X_Ca= 0.10–0.28)-bearing assemblages in pelitic schists, and represents the highest-grade zone of the Sanbagawa metamorphic terrain. Mineral assemblages in pelitic schists of this zone, all with quartz, sodic plagioclase, muscovite and clinozoisite (or zoisite), are garnet + biotite + chlorite + paragonite, garnet + biotite + hornblende + chlorite, and partial assemblages of these two types. Correlations between mineral compositions, mineral assemblages and mineral stability data assuming PH₂O = P_solid suggests that metamorphic conditions of this zone are about 610 ± 25°C and 10 ± 1 kbar.
Based upon a comparative study of mineralogy and chemistry of pelitic schists in the oligoclase-biotite zone of the Sanbagawa terrain with those in the New Caledonia omphacite zone as an example of a typical high-pressure type of metamorphic belt and with those in a generalized'upper staurolite zone'as an example of a medium-pressure type of metamorphic belt, progressive assemblages within these three zones can be related by reactions such as:     

Decompression-induced growth of albite porphyroblasts, Fleur de Lys Supergroup, western Newfoundland

Abstract Albite porphyroblasts are widely distributed in pelitic and semi-pelitic schists of the Fleur de Lys Supergroup, western Newfoundland. Textures and mineral assemblages indicate that albite grew during nearly isothermal decompression from P-T conditions of about 500° C, 9 kbar, to conditions of 550° C, 6.5 kbar. Three compositional varieties of albite-bearing schists, here termed PMAQ (paragonite-muscovite-albite-quartz), MMAQ (microcline-muscovite-albite-quartz), and PMMQ (paragonite-muscovite-margarite-quartz), can be distinguished on the basis of pre-porphyroblast mineral assemblages. Analysis of these assemblages in terms of the composition of the coexisting fluid [log a (Na⁺/H⁺) versus log a (K⁺/H⁺)] suggests that, as pressure and temperature changed, the stability field of albite expanded at the expense of coexisting matrix phyllosilicates. This promoted growth of albite on pre-existing or newly formed nuclei. Late oligoclase in PMAQ and PMMQ samples is associated with replacement of matrix garnet by plagioclase + mica ° Chlorite, particularly in strongly sheared samples.     

Petrographic Characteristics and Alteration Geochemistry of Granite-hosted Tungsten Mineralization at Degana, NW India

Abstract. Vein type tungsten mineralization at Degana is genetically and spatially associated with the Degana Granite. The deposit is characterized by pervasive wall rock alteration around the mineralized quartz veins. Laterally three different alteration zones, greisen, silicification and potassic zones, are marked based on the field features, mineral assemblages and geo-chemical characteristics. In the present paper, systematic mineralogical and chemical variation in these alteration zones is reported. Thick mono-mineralic (zinnwaldite) selvages around the veins characterize the deposit. Plagioclase and alkali feldspar are low in the greisen zones while K-feldspar shows more increase than plagioclase in the potassic zone. Quartz is uniformly high in all the alteration zones, but it shows an anomalous value in the silicification zone. Al₂O₃ concentration shows initial depletion in greisen zone with gradual increase away from the contact. MgO and FeO are higher in greisen zone than silicification and potassic zones. The potassic zone is characterized by the depletion of Na₂O and higher value of K₂O.
The common presence of topaz and fluorite as both primary and secondary minerals and fluorine-bearing micas suggest fluorine partitioning in substantial amount between granitic melt and coexisting aqueous fluid phase and higher HF activity during the evolution of hydrothermal fluid. The mutual relationship of the fluorine minerals (topaz and fluorite) in the different alteration zones suggests an increase in the Ca²⁺ activity and decrease of H+ activity during the fluid evolution from greisenization towards alkali-metasomatised granite and the fluid is assumed to change from low to high activity ratio of Ca²⁺/H+.     

Phase equilibria in the hornblende-bearing basic gneisses of the Uvete area, central Kenya

Abstract The hornblende-bearing basic gneisses in the Uvete area, central Kenya, were metamorphosed under a narrow range of P and T (6.5 ± 0.5kbar and 530 ± 40°C) of the staurolitekyanite zone in the Mozambique metamorphic belt. They show a wide variety of divariant and trivariant mineral assemblages consisting of hornblende, cumminatonite, gedrite, anthophyllite, chlorite, garnet, epidote, clinopyroxene, plagio-clase and quartz. The bulk and mineral chemistries and the graphical representation of phase relations show that each mineral assemblage approaches chemical equilibrium and defines a unique composition volume in the A'(Al + Fe³⁺− (13/7)Na)-F(Fe²⁺)-M'(Mg)-C'(Ca-(3/7)Na) tetrahedron. The composition volumes are distributed quite regularly and do not overlap each other.
The phase relations in the Uvete area are in contrast with those in the staurolite-kyanite zone amphibolites in the Mt. Cube quadrangle, Vermont. The amphibolites there contain low-variance mineral assemblages formed under different values of μ_H2O and μ_CO2. These assemblages define overlapping composition volumes in the A'-F'-M'-C'tetrahedron.
The mineral assemblages in the Uvete area are interpreted as having formed in equilibrium with fluid at a high and nearly constant μH₂O value. Such a fluid composition was externally controlled by the supply of H₂O-rich fluid expelled from the surrounding pelitic and psammitic rocks. The body size of the basic gneisses in the Uvete area (less than 400m in thickness) was small enough for the fluid to migrate completely.     

Aluminum silicates in the Mount Raleigh pendant, British Columbia

In regionally metamorphosed pelites of the Mount Raleigh pendant, the fibrolite isograd occurs 5km downgrade from the sillimanite isograd. Fibrolite formed from the decomposition of biotite, a reaction that probably resulted from the late-stage influx of acidic volatiles. In contrast, sillimanite formed by the direct,'volume-for-volume'replacement of andalusite. Andalusite and sillimanite coexist in a 3 km-wide zone above the sillimanite isograd. Electron probe analyses of these phases reveal low minor element contents and yield K _D [= X ] values close to unity; the low Fe₂O₃ contents are compatible with reducing conditions implied by the ubiquity of graphite. Because K _D → 1.0, the zone of coexisting andalusite + sillimanite cannot be attributed to multivariancy resulting from partitioning of minor elements between these phases. Rather, the metastable persistence of andalusite into the sillimanite P-T stability field is suggested. The modal proportions of sillimanite versus andalusite imply that minimal (<5%) and alusitesillimanite reaction occurred in a zone 1.5km above the sillimanite isograd; in contrast, there was a marked increase in reaction progress immediately above this zone. With an estimated thermal gradient (in the plane of exposure) of approximately 20°C/km, the 1.5 km-wide zone of nil reaction suggests that the andalusite-sillimanite equilibrium boundary was overstepped by about 30 °C before significant reaction occurred. Inclusion-rich areas in andalusite provided favourable sites for sillimanite nucleation ; however, the growth of sillimanite may have been impeded by'pinning'of sillimanite grain boundaries by inclusions.     

P-T-X (CO2) conditions in mafic and calc-silicate hornfelses from Oberon, New South Wales, Australia

Abstract The Rockley Volcanics from near Oberon, New South Wales occur within the aureole of the Carboniferous Bathurst Batholith and have been contact metamorphosed at P ∼ 100 ± 50MPa (10.5kbar) and a maximum T ∼ 565°C in the presence of a C–O–H fluid. Prior to contact metamorphism the volcanics were regionally metamorphosed and altered with the extensive development of actinolite, chlorite, plagioclase, quartz and calcite. The contact metamorphosed equivalents of these rocks have been subdivided into: Ca-poor (cordierite + gedrite), Mg-rich (amphibole + olivine + spinel), mafic (amphibole + plagioclase) and Ca-rich (amphibole + garnet + diopside; diopside + plagioclase; garnet + diopside + wollastonite) rocks.
The chemistry of the minerals in the hornfelses was controlled by the bulk rock chemistry and fluid composition. Pargasites and hastingsites as well as an unusual phlogopite with blue green pleochroism, are found in Ca-rich hornfelses. A comparison of the assemblages with experimentally derived equilibria suggests that the fluid phase associated with the Ca-rich hornfelses was water-rich (X_co2= 0.1 to 0.3) while that associated with the Mg-rich hornfelses was enriched in CO₂ (X_co2 > 0.7). The different hornfels types have reacted to contact metamorphism independently in both their solid and fluid chemistries.     

The pressure dependence of the zirconium-in-rutile thermometer

The solubility of ZrO₂ in rutile is strongly temperature-dependent and has been identified as a potentially powerful thermometer when the rutile coexists with an appropriate buffer assemblage, e.g. zircon + quartz. In combination with experimental data at 10 kbar, previous consideration of data on natural rutile has not identified a pressure dependence for the thermometer. However, the expected volume change as a result of substitution of the larger Zr⁴⁺ cation for Ti⁴⁺ suggests that the Zr content of rutile should decrease with increasing pressure. To investigate the pressure dependence of the thermometer, piston cylinder (at 10, 20 & 30 kbar) and 1 atm furnace experiments were performed in the system ZrO₂-TiO₂-SiO₂. The solubility of ZrO₂ in rutile, in the presence of zircon and quartz was reversed at each pressure value. From these experiments, the thermodynamics of the end-member reaction ZrSiO₄ = SiO₂ + ZrO₂ (in rutile) have been determined. There is a secondary pressure effect accompanying the primary temperature dependence of the Zr content of rutile. New thermometer equations are, in the α -quartz field: in the β -quartz field and in the coesite field in which φ is ppm Zr, P is in kbar and R is the gas constant, 0.0083144 kJ K⁻¹. Thermometric results using these equations are shown for a range of geological settings.     

A ternary solid solution model for omphacite and its application to geothermobarometry of eclogites from the Middle Adula nappe (Central Alps, Switzerland)

A ternary solid solution model for omphacite with the end-members jadeite (NaAlSi₂O₆), diopside (CaMgSi₂O₆) and hedenbergite (CaFeSi₂O₆) was derived from experimental data from the literature. The subregular solution model, fitted by linear programming, is best suited to omphacites with very little aegirine component in common eclogites. Applying this solution model to the calculation of equilibrium phase diagrams of eclogites from the Adula nappe (Central Alps, Switzerland) results in large stability fields for common eclogite assemblages (garnet+omphacite+quartz+H₂O±kyanite). Within this field the compositions of garnet and omphacite show very little variation. A precise determination of the peak-pressure and temperature is not possible. The occurrence of amphibole, overgrowing the peak-pressure assemblage in fresh eclogite, suggests retrograde re-equilibration, still under eclogite facies conditions. The computation of isopleths for garnet and pyroxene end-members allows the estimation of the pressure and temperature conditions of this re-equilibration event (19–21  kbar, c .  700 °C).