Melting and phase relations in the plane tholeiite-lherzolite-nepheline basanite to 40 kilobars with geological implications

Six crystalline mixtures, picrite, olivine-rich tholeiite, nepheline basanite, alkali picrite, olivine-rich basanite, and olivine-rich alkali basalt were recrystallized at pressures to 40 kb, and the phase equilibria and sequences of phases in natural basaltic and peridotitic rocks were investigated.The picrite was recrystallized along the solidus to the assemblages (1) olivine+orthopyroxene+ clinopyroxene +plagioclase+spinel below 13 kb, (2) olivine+orthopyroxene+clinopyroxene+spinel between 13 kb and 18 kb, (3) olivine+orthopyroxene+clinopyroxene+ garnet+spinel between 18 kb and 26 kb, and (4) olivine+clinopyroxene+garnet above 26 kb. The solidus temperature at 1 atm is slightly below 1,100° and rises to 1,320° at 20 kb and 1,570° at 40 kb. Olivine is the primary phase crystallizing from the melt at all pressures to 40 kb.The olivine-rich tholeiite was recrystallized along the solidus into the assemblages (1) olivine+ clinopyroxene+plagioclase+spinel below 13 kb, (2) clinopyroxene+orthopyroxene+ spinel between 13 kb and 18 kb, (3) clinopyroxene+garnet+spinel above 18 kb. The solidus temperature is slightly below 1,100° at 1 atm, 1,370° at 20 kb, and 1,590° at 40 kb. The primary phase is olivine below 20 kb but is orthopyroxene at 40 kb.In the nepheline basanite, olivine is the primary phase below 14 kb, but clinopyroxene is the first phase to appear above 14 kb. In the alkali-picrite the primary phase is olivine to 40 kb. In the olivine-rich basanite, olivine is the primary phase below 35 kb and garnet is the primary phase above 35 kb. In the olivine-rich alkali basalt the primary phase is olivine below 20 kb and is garnet at 40 kb.Mineral assemblages in a granite-basalt-peridotite join are summarized according to reported experimental data on natural rocks. The solidus of mafic rock is approximately given by T=12.5 P _Kb+1,050°. With increasing pressure along the solidus, olivine disappears by reaction with plagioclase at 9 kb in mafic rocks and plagioclase disappears by reaction with olivine at 13 kb in ultramafic rocks. Plagioclase disappears at around 22 kb in mafic rocks, but it persists to higher pressure in acidic rocks. Garnet appears at somewhat above 18 kb in acidic rocks, at 17 kb in mafic rocks, and at 22 kb in ultramafic rocks.The subsolidus equilibrium curves of the reactions are extrapolated according to equilibrium curves of related reactions in simple systems. The pyroxene-hornfels and sanidinite facies is the lowest pressure mineral facies. The pyroxene-granulite facies is an intermediate low pressure mineral facies in which olivine and plagioclase are incompatible and garnet is absent in mafic rocks. The low pressure boundary is at 7.5 kb at 750° C and at 9.5 kb at 1,150° C. The high pressure boundary is 8.0 kb at 750° C and 15.0 kb at 1,150° C. The garnet-granulite facies is an intermediate high pressure facies and is characterized by coexisting garnet and plagioclase in mafic rocks. The upper boundary is at 10.3 kb at 750° C and 18.0 kb at 1,150° C. The eclogite facies is the highest pressure mineral facies, in which jadeite-rich clinopyroxene is stable.Compositions of minerals in natural rocks of the granulite facies and the eclogite facies are considered. Clinopyroxenes in the granulite-facies rocks have smaller jadeite-Tschermak's molecule ratios and higher amounts of Tschermak's molecule than clinopyroxenes in the eclogite-facies rocks. The distribution coefficients of Mg between orthopyroxene and clinopyroxene are normally in the range of 0.5–0.6 in metamorphic rocks in the granulite facies. The distribution coefficients of Mg between garnet and clinopyroxene suggest increasing crystallization temperature of the rocks in the following order: eclogite in glaucophane schist, eclogite and granulite in gneissic terrain, garnet peridotite, and peridotite nodules in kimberlite.Temperatures near the bottom of the crust in orogenic zones characterized by kyanitesillimanite metamorpbism are estimated from the mineral assemblages of metamorphic rocks in Precambrian shields to be about 700° C at 7 kb and 800° C at 9 kb, although heat-flow data suggest that the bottom of Precambrian shield areas is about 400° C and the eclogite facies is stable.The composition of liquid which is in equilibrium with peridotite is estimated to be close to tholeiite basalt at the surface pressure and to be picrite at around 30 kb. The liquid composition becomes poorer in normative olivine with decreasing pressure and temperature.During crystallization at high pressure, olivine and orthopyroxene react with liquid to form clinopyroxene, and a discontinuous reaction series, olivine orthopyroxene clinopyroxene is suggested. By fractional crystallization of pyroxenes the liquid will become poorer in SiO₂. Therefore, if liquid formed by partial melting of peridotite in the mantle slowly rises maintaining equilibrium with the surrounding peridotite, the liquid will become poorer in MgO by crystallization of olivine, and tholeiite basalt magma will arrive at the surface. On the other hand, if the liquid undergoes fractional crystallization in the mantle, the liquid may change in composition to alkali-basalt magma and alkali-basalt volcanism may be seen at a late stage of volcanic activity.Publication No. 681, Institute of Geophysics and Planetary Physics, University of California, Los Angeles.     

Iron-Titanium Oxide Geothermometry and Petrogenesis of Lava Flows and Dykes from Mandla Lobe of the Eastern Deccan Volcanic Province, India

Compositional studies on different forms of magnetite, ulvospinel, ilmenite and hematite mineral phases occurring in 37 lava flows and 6 dykes of the Mandla lobe are presented in this paper. Ilmenite (0001) in equilibrium with titanomanetite show high values of temperature of equilibration, ranging from 1172–974°C, for high alumina quartz normative tholeiitic lava flows of Chemical Type - A; 1129–1229°C for low alumina quartz normative tholeiitic lava flows of Chemical Type - B; 1283–1124°C for tholeiitic lava flows of Chemical Type - F and 1243°C and 99O°C for two diopside olivine normative tholeiite flows of Chemical Type D. High olivine normative flows of Chemical Type - G and H show 1095°C and 1092°C respectively. Whereas, high hypersthene normative tholeiite flow of Chemical me C shows temperature of 1187°C. Data plots disposition over iron-titanium oxide equilibration temperature vs – logfo₂, diagram for Mandla lava flows and other parts of the Deccan (Igatpuri, Mahabaleshwer, Nagpur and Sagar areas) revealed that tholeiitic (evolved) basalt of the eastern Deccan volcanic province formed at high temperatures whereas, picritic (primitive) lavas of Igatpuri and tholeiitic basalt of Mahabaleshwar areas were formed at low temperatures. Mahabaleshwer basalts follow FMQ (fayalite-magnetite-quartz) buffer curve but, plots of the Mandla basalts lie above this curve indicating higher temperatures of crystallisation of ilmenite-titanomagnetite than that of the lava flows from other parts of Deccan 'Raps. The eastern Deccan Traps are most evolved types of lava as characterised by its low Mg-number and Ni content whereas, Igatpuri lava flows are picritic (primitive), having high Mg-number and Ni contents. Temperature vs FeO + Fe₂O₃ / FeO + Fe₂O₃ + MgO ratio data plots for Mandla and other Deccan lava flows and liquidus data for Hawaiian tholeiites, indicated that Igatpuri basalts lie parallel to the liquidus line of Hawaiian tholeiite but at lower temperatures. Large data plots of Mandla lava flows lie along the liquidus line of the Hawaiian lava. The highly vesicular nature of compound lava flows having large amount of volatile is responsible for low temperature values whereas, lava flows represented by high temperatures show high modal values of glass and opaque minerals.     

The Cold Bay Volcanic Center,Aleutian Volcanic arc

The widespread abundance of Hi-Alumina Basalt (HAB) lavas in most volcanic arcs has been suggested by some as evidence for a primary, parental HAB magma generated by the high pressure melting of subducted oceanic crust (quartz eclogite). Others suggest a parental, mantle-derived olivine tholeiite magma which produces HAB magmas through fractionation of olivine, clinopyroxene, chrome-spinel +/– plagioclase. The petrology and geochemistry of seven HAB lavas from the Aleutian Cold Bay Volcanic Center have been studied in order to specifically address these two possibilities. All lavas show mineralogical and compositional features typical of most Aleutian HAB lavas. Coexisting opx and cpx in a closely associated basaltic-andesite indicate a minimum pre-eruption temperature of 1,110° C. A comparison of the observed (plag-tmag-olivcpx) and experimentally determined crystallization sequences yields a minimum pre-eruption pressure estimate of 7 kb and estimated H₂O contents of 0.7 wt.%. Maximum pre-eruption f _{o 2} values have been estimated at NNO+0.6 log units.Mass balance calculations demonstrate that the HAB compositions are satisfied by the fractionation of olivine, clinopyroxene +/– plagioclase from a primitive (Mg-# > 65) parental tholeiite. Plagioclase accumulation does not play a significant role in their origin. Many of the same compositional characteristics are also satisfied by high pressure melting of altered ocean ridge tholeiite +5 v.% pelagic sediment (quartz eclogite). The available HAB phase equilibria data do not support a fractionation origin but do support an origin involving high pressure melting of quartz eclogite. The lack of compositional zonation in the HAB phenocrysts, and the complete absence of disequilibrium MgO-rich mafic phenocrysts further argue against a tholeiite fractionation origin.Consideration of all these features indicates that the geochemical data are permissive in their interpretation. A process involving tholeiite fractionation successfully predicts the compositions of the HAB lavas but is at odds with the mineralogical and phase equilibria evidence. With some exceptions (notably Ni, Cr and Sr abundances), a process of high pressure quartz eclogite melting is consistent with the compositional, mineralogical and phase equilibria characteristics of these HAB lavas. When the relative merits of both origins are weighed it is apparent that a quartz eclogite source satisfies more of important features of these HAB lavas.Extrusive rocks have been grouped on a basis of SiO₂ content into basalt (<52 wt.%), basaltic-andesite (52–56 wt.%) and andesite (>56 wt.%) after Ewart (1982)     

Origin of ultramafic xenoliths containing exsolved pyroxenes from Hualalai Volcano,Hawaii

Hualalai Volcano, Hawaii, is best known for the abundant and varied xenoliths included in the historic 1800 Kaupulehu alkalic basalt flow. Xenoliths, which range in composition from dunite to anorthosite, are concentrated at 915-m elevation in the flow. Rare cumulate ultramafic xenoliths, which include websterite, olivine websterite, wehrlite, and clinopyroxenite, display complex pyroxene exsolution textures that indicate slow cooling. Websterite, olivine websterite, and one wehrlite are spinel-bearing orthopyroxene +olivine cumulates with intercumulus clinopyroxene +plagioclase. Two wehrlite samples and clinopyroxenite are spinel-bearing olivine cumulates with intercumulus clinopyroxene+orthopyroxene + plagioclase. Two-pyroxene geothermometry calculations, based on reconstructed pyroxene compositions, indicate that crystallization temperatures range from 1225° to 1350° C. Migration or unmixing of clinopyroxene and orthopyroxene stopped between 1045° and 1090° C. Comparisons of the abundance of K₂O in plagioclase and the abundances of TiO₂ and Fe₂O₃in spinel of xenoliths and mid-ocean ridge basalt, and a single ⁸⁷Sr/ ⁸⁶Sr determination, indicate that these Hualalai xenoliths are unrelated to mid-ocean ridge basalt. Similarity between the crystallization sequence of these xenoliths and the experimental crystallization sequence of a Hawaiian olivine tholeiite suggest that the parental magma of the xenoliths is Hualalai tholeiitic basalt. Xenoliths probably crystallized between about 4.5 and 9 kb. The 155°–230° C of cooling which took place over about 120 ka — the age of the youngest Hualalai tholeiitic basalt — yield maximum cooling rates of 1.3×10^–3–1.91×10^–3 °C/yr. Hualalai ultramafic xenoliths with exsolved pyroxenes crystallized from Hualalai tholeiitic basalt and accumulated in a magma reservoir located between 13 and 28 km below sealevel. We suspect that this reservoir occurs just below the base of the oceanic crust at about 19 km below sealevel.     

Experimental studies to constrain parental magma of Malangtoli volcanics from Singhbhum craton of the eastern Indian shield

Malangtoli volcanics of the Singhbhum craton of the eastern Indian shield is one of the important Proterozoic lava suites. Experimental studies on 1 atmosphere pressure constrain the parental magma type and temperature range of crystallization of the parent magma (deduced to be in the range of 1500°C to 1200°C). The experimental studies show that at 1500°C, plagioclase is the first phase to crystallize, followed by few opaques which join along with plagioclase at 1450°C. At subsequent lower temperature (1400°C-1300°C), plagioclase and opaque continue to crystallize. At 1250°C plagioclase and opaque still persist while pyroxene appears first and liquid (glass) still remains. Appearance of opaque minerals (magnetite and illmenite) at both ~1400°C and ~1300°C indicate oscillation of oxygen fugacity in the parent magma, petrographically documented by coarser phenocrysts as well as finer or peripheral tiny grains. Use of tectonic discrimination diagrams (based on discrimination factors F₁-F₂ and FeO^t/MgO vs. TiO₂) shows an island arc tholeiitic affinity for Malangtoli volcanic, suggests that the role of proto-plate convergence in Singhbhum architecture played an important role to build up Malangtoli volcanics during Proterozoic.     

The Influence of Sodium and Potassium Chlorides on Phase Ratios in the Eclogite–CaCO3–H2O + CO2 System at 4 GPa and 1200–1300°C

To characterize the influence of alkaline metal chlorides on the phase ratios under melting of upper mantle eclogites, the eclogite–CaCO₃–NaCl–KCl system with Н₂О + СО₂-fluid was studied in the experiments under 4 GPa and 1200–1300°C. A low difference in temperatures (<100°C) was registered between the eclogite solidus and liquidus (>1200 and <1300°C, respectively), which is characteristic for the near-eutectic compositions. The phase proportions were peculiar for the absence of any silicate melt over the entire temperature range considered. The carbonate melt coexisted with clinopyroxene and garnet within 1200–1250°C, whereas a carbonate melt exclusively occurred under above-liquidus conditions at 1300°C. The melt quenching resulted in the formation of a multiphase fine-grained mixture of Ca, Na, and K carbonates and chlorides containing microinclusions of clinopyroxene and garnet. The occurrence of a high-calcium carbonate melt in Cl-containing eclogite systems might play a significant role in the mantle metasomatism of subduction zones characterized by the water–alkaline–chloride type of fluids.

     

Fe-rich tholeiitic liquids and their cumulate products in the Pleasant Bay layered intrusion, coastal Maine

Fe-rich tholeiitic liquids are preserved as chilled pillows and as the chilled base of a 27 meter thick macrorhythmic layer in the Pleasant Bay mafic-silicic layered intrusion. The compositions of olivine (Fo₁) and plagioclase (An₁₃₋₈) in these extremely fine grained rocks suggest that they represent nearly end stage liquids that formed by fractionation of tholeiitic basalt. Their major element compositions (∼17.5 wt% FeO_T and 54 wt%SiO₂) closely resemble highly evolved glasses in the Loch Ba ring dike and some recent estimates of end-stage liquids related to the Skaergaard layered intrusion, and are consistent with recent experimental studies of tholeiite fractionation. Their trace element compositions are consistent with extensive earlier fractionation of plagioclase, olivine, clinopyroxene, ilmenite, magnetite and apatite. The mineral assemblage of the chilled rocks (olivine, clinopyroxene, quartz, ilmenite and magnetite), apatite saturation temperatures, and very low Fe³⁺/Fe²⁺indicate conditions of crystallization at temperatures of about 950 °C and f _{O 2} about two log units below FMQ. Cumulates that lie about 3 meters above the chilled base of the macrorhythmic layer contain cumulus plagioclase, olivine, clinopyroxene, ilmenite, apatite and zircon. This mineral assemblage and the Fe-Mg ratio in clinopyroxene cores suggest that this cumulate was in equilibrium with a liquid having a composition identical to that of the chilled margin which lies directly beneath it. The high FeO_T and low SiO₂ concentrations of this cumulate (23.3 and 45.8 wt%, respectively) are comparable to those in late stage cumulates of the Skaergaard and Kiglapait intrusions. This association of a chilled liquid and cumulate in the Pleasant Bay intrusion suggests that late stage liquids in tholeiitic layered intrusions may have been more SiO₂-rich than field-based models suggest and lends support to recent experimental studies of tholeiite fractionation at low f _O2 which indicate that saturation of an Fe-Ti oxide phase should cause FeO_T to decrease in the remaining liquid. Received: 17 January 1997 / Accepted: 10 June 1997     

Partial transformation of gabbro to coesite-bearing eclogite from Yangkou, the Sulu terrane, eastern China

An ultra-high-pressure (UHP) metamorphic slab at Yangkou Beach near Qingdao in the Sulu region of China consists of blocks of eclogite facies metagabbro, metagranitoid, ultramafic rock and mylonitic orthogneisses enclosed in granitic gneiss. A gradational sequence from incipiently metamorphosed gabbro to completely recrystallized coesite eclogite formed at ultra-high-pressures was identified in a single 30 m block; metagabbro is preserved in the core whereas coesite eclogite occurs along the block margins. The metagabbro contains an igneous assemblage of Pl+Aug+Opx+Qtz+Bt+Ilm/Ti-Mag; it shows relict magmatic textures and reaction coronas. Fine-grained garnet developed along boundaries between plagioclase and other phases; primary plagioclase broke down to Ab+Ky+Ms+Zo±Grt±Amp. Augite is rimmed by sodic augite or omphacite, whereas orthopyroxene is rimmed by a corona of Cum±Act and Omp+Qtz layers or only Omp+Qtz. In transitional rocks, augite and orthopyroxene are totally replaced by omphacite, and the lower-pressure assemblage Ab+Ky+Phn+Zo+Grt coexists with domains of Omp (Jd_70–73)+Ky±Phn in pseudomorphs after plagioclase. Both massive and weakly deformed coesite-bearing eclogites contain Omp+Ky+Grt+Phn+Coe/Qtz+Rt, and preserve a faint gabbroic texture. Coesite inclusions in garnet and omphacite exhibit limited conversion to palisade quartz; some intergranular coesite and quartz pseudomorphs after coesite also occur. Assemblages of the coronal stage, transitional and UHP peak occurred at about 540±50 °C at c. 13 kbar, 600–800 °C at ≥15–25 kbar and 800–850 °C at >30 kbar, respectively. Garnet from the coronal- through the transitional- to the eclogite-stage rocks show a decrease in almandine and an increase in grossular±pyrope components; garnet in low-grade rocks contains higher MnO and lower pyrope components. The growth textures of garnet within pseudomorphs after plagioclase or along grain boundaries between plagioclase and other phases are complex; the application of garnet zoning to estimate P–T should be carried out with caution. Some garnet enclosing quartz aggregates as inclusions shows radial growth boundaries; these quartz aggregates, as well as other primary and low-P phases, persisted metastably at UHP conditions due to sluggish reactions resulting from the lack of fluid during prograde and retrograde P–T evolution.     

Petrology and Petrogenesis of Cumulate Peridotites and Gabbros from the Marum Ophiolite Complex, Northern Papua New Guinea

The Marum ophiolite complex in northern Papua New Guinea includesa thick (3–4 km) sequence of ultramafic and mafic cumulates,which are layered on a gross scale from dunite at the base upwardsthrough wehrlite, lherzolite, plagioclase lherzolite, pyroxenite,olivine norite-gabbro and norite-gabbro to anorthositic gabbroand ferrogabbro at the top. Igneous layering and structures,and cumulus textures indicate an origin by magmatic crystallizationin a large magma chamber(s) from magma(s) of evolving composition.Most rocks however show textural and mineralogical evidenceof subsolidus re-equilibration. The cumulate sequence is olivine and chrome spinel followedby clinopyroxene, orthopyroxene and plagioclase, and the layeredsequence is similar to that of the Troodos and Papuan ophiolites.These sequences differ from ophiolites such as Vourinos by thepresence of cumulus magnesian orthopyroxene, and are not consistentwith accumulation of low pressure liquidus phases of mid-oceanridge-type olivine tholeiite basalts. The cumulus phases show cryptic variation from Mg- and Ca-richearly cumulates to lower temperature end-members, e.g. olivineMg_93–78, plagioclase An_94–63. Co-existing pyroxenesdefine a high temperature solidus with a narrower miscibilitygap than that of pyroxenes from stratiform intrusions. Re-equilibratedpyroxene pairs define a low-temperature, subsolidus solvus.Various geothermometers and geobarometers, together with thermodynamiccalculations involving silica buffers, suggest the pyroxene-bearingcumulates crystallized at 1200 °C and 1–2 kb pressureunder low f_O2. The underlying dunites and chromitites crystallizedat higher temperature, 1300–1350 °C. The bulk of thecumulates have re-equilibrated under subsolidus conditions:co-existing pyroxenes record equilibration temperatures of 850–900°C whereas olivine-spinel and magnetite-ilmenite pairs indicatefinal equilibration at very low temperatures (600 °C). Magmas parental to the cumulate sequence are considered to havebeen of magnesian olivine-poor tholeiite composition (>50per cent SiO₂, 15 per cent MgO, 100 Mg/(Mg + Fe²⁺) 78) richin Ni and Cr, and poor in TiO₂ and alkalies. Fractionated examplesof this magma type occur at a number of other ophiolites withsimilar cumulate sequences. Experimental studies show that suchlavas may result from ial melting of depleted mantle lherzoliteat shallow depth. The tectonic environment in which the complexformed might have been either a mid-ocean ridge or a back-arebasin.     

Petrological implications of some corona structures

Reactions between olivine and plagioclase, and between pyroxenes and plagioclase, commonly produce corona assemblages of lower volume and entropy. These coronas imply that assemblages representative of intermediate-and high-pressure granulite facies, and of eclogite facies (emphacite + garnet), can be produced by the cooling of dry olivine + plagioclase and pyroxene + plagioclase assemblages from igneous temperatures within the continental crust. They further imply that eclogite is a stable assemblage within the deeper parts of the continental crust; this in turn requires that dP/dT > 0 for the equilibrium curves for the relevant reactions. The general relations between T and rates of nucleation, growth and diffusion suggest that these coronas will only be formed in relatively deep-seated rocks (P > 6 kb ?). The formation of such coronasby regional or contact metamorphism, or by metasomatism, is unlikely; they are best regarded as retrograde features.     

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.     

HFSE-rich picritic rocks from the Mino accretionary complex,southwestern Japan

Sills, pillow lavas and hyaloclastites of the HFSE-rich picrite and related rocks (ankaramite and basanite) occur in the Middle Permian cherts in the Mino Jurassic accretionary complex, southwestern Japan. These rocks show systematic trace element patterns enriched in incompatible elements, which indicate that the associated ankaramite and basanite are formed by the crystal fractionation from the picrite. The presence of the hyaloclastite in the chert sequence covering a large tholeiitic greenstone body indicates that the picrite was produced in an intraoceanic setting in the Middle Permian time subsequent to the extrusion of the voluminous oceanic island tholeiite. The Mino picrites resemble the Siberian meimechite and Polynesian picrites in its HFSE-rich chemical composition. The HFSE enrichment in these picrites cannot be explained by low degree of partial melting of primitive peridotite mantle only, and needs a source material involving recycled oceanic crust (eclogite). The differences in MgO content and in TiO₂/Al₂O₃ and Zr/Y ratios among the HFSE-rich picrites indicate that the melting pressure increases from the Polynesian picrite through Mino picrite to Siberian picrite. This may reflect the increasing thickness of the overlying lithosphere at the time and place of magmatism. The HFSE-rich picrites may be a product of a superplume event. The presence of HFSE-rich picrite in Mino and Siberia indicate that the superplume activities occur in both continental and oceanic settings in the Permian time.     

Neoproterozoic tholeiitic arc plutonism: petrology of gabbroic intrusions in the El-Aradiya area,Eastern Desert,Egypt

Gabbroic intrusions of the El-Aradiya area are a part of the Neoproterozoic basement cropping out in the central Eastern Desert of Egypt. They are composed mainly of gabbroic cumulates (diopside-plagioclase cumulate and plagioclase-augite cumulate) and fine-grained noncumulate gabbro. Mineral chemistry data indicate that the plagioclase core compositions of the gabbroic cumulates range between An₉₀ and An₆₀, whereas fine-grained noncumulate gabbro plagioclase core compositions are An₆₁₋₅₆ and rim compositions are An₅₄₋₄₂. The clinopyroxenes are diopside and augite in the gabbroic cumulate, and augite in the fine-grained noncumulate gabbro. Chemical re-equilibration between pyroxenes of gabbroic cumulates vary from 1150-900°C and for fine-grained noncumulate gabbro range from 1200-1100°C. The amphiboles are calcic, varying from tschermakite and tschermakitic hornblende, and Mg-hornblende in the gabbroic cumulate and only Mg-hornblende in the fine-grained noncumulate gabbro. They indicate an island-arc tholeiitic setting for gabbroic intrusions of the El-Aradiya area. Major and trace element data suggest arc tholeiite characters, a comagmatic suite and subduction-related magma with enrichment of LILE and depletion in HFSE relative to MORB. The estimated parent magma is similar to tholeiitic Aleutian arc primary magma. The gabbroic intrusions are analogous to intrusions emplaced in an immature island-arc setting in which the oceanic crust was thin.     

Prograde and retrograde history of eclogites from the Eastern Blue Ridge, North Carolina, USA

Abstract The prograde metamorphism of eclogites is typically obscured by chemical equilibration at peak conditions and by partial requilibration during retrograde metamorphism. Eclogites from the Eastern Blue Ridge of North Carolina retain evidence of their prograde path in the form of inclusions preserved in garnet. These eclogites, from the vicinity of Bakersville, North Carolina, USA are primarily comprised of garnet–clinopyroxene–rutile–hornblende–plagioclase–quartz. Quartz, clinopyroxene, hornblende, rutile, epidote, titanite and biotite are found as inclusions in garnet cores. Included hornblende and clinopyroxene are chemically distinct from their matrix counterparts. Thermobarometry of inclusion sets from different garnets record different conditions. Inclusions of clinozoisite, titanite, rutile and quartz (clinozoisite + titanite = grossular + rutile + quartz + H₂O) yield pressures (6–10 kbar, 400–600 °C and 8–12 kbar 450–680 °C) at or below the minimum peak conditions from matrix phases (10–13 kbar at 600–800 °C). Inclusions of hornblende, biotite and quartz give higher pressures (13–16 kbar and 630–660 °C). Early matrix pyroxene is partially or fully broken down to a diopside–plagioclase symplectite, and both garnet and pyroxene are rimmed with plagioclase and hornblende. Hypersthene is found as a minor phase in some diopside + plagioclase symplectites, which suggests retrogression through the granulite facies. Two‐pyroxene thermometry of this assemblage gives a temperature of c. 750 °C. Pairing the most Mg‐rich garnet composition with the assemblage plagioclase–diopside–hypersthene–quartz gives pressures of 14–16 kbar at this temperature. The hornblende–plagioclase–garnet rim–quartz assemblage yields 9–12 kbar and 500–550 °C. The combined P–T data show a clockwise loop from the amphibolite to eclogite to granulite facies, all of which are overprinted by a texturally late amphibolite facies assemblage. This loop provides an unusually complete P–T history of an eclogite, recording events during and following subduction and continental collision in the early Palaeozoic.     

Metamorphic Evolution of Iron-rich Mafic Cumulates from the Otztal-Stubai Crystalline Complex, Eastern Alps, Austria

Olivine-rich rocks containing olivine + orthopyroxene + spinel+ Ca-amphibole ± clinopyroxene ± garnet are presentin the central Ötztal–Stubai crystalline basementassociated with eclogites of tholeiitic affinity. These rockscontain centimetre-sized garnet layers and lenses with garnet+ clinopyroxene ± corundum. Protoliths of the olivine-richrocks are thought to be olivine + orthopyroxene + spinel dominatedcumulates generated from an already differentiated Fe-rich () tholeiitic magma that was emplaced into shallowcontinental crust. Protoliths of the garnet-rich rocks are interpretedas layers enriched in plagioclase and spinel intercalated ina cumulate rock sequence that is devoid of, or poor in, plagioclase.U–Pb sensitive high-resolution ion microprobe dating ofzircons from a garnet layer indicates that emplacement of thecumulates took place no later than 517 ± 7 Myr ago. Aftertheir emplacement, the cumulates were subjected to progressivemetamorphism, reaching eclogite-facies conditions around 800°Cand >2 GPa during a Variscan metamorphic event between 350and 360 Ma. Progressive high-P metamorphism induced breakdownof spinel to form garnet in the olivine-rich rocks and of plagioclase+ spinel to form garnet + clinopyroxene ± corundum inthe garnet layers. Retrogressive metamorphism at T 650–680°Cled to the formation of Ca-amphibole, chlorite and talc in theolivine-rich rocks. In the garnet layers, högbomite formedfrom corundum + spinel along with Al-rich spinel, Ca-amphibole,chlorite, aspidolite–preiswerkite, magnetite, ilmeniteand apatite at the interface between olivine-rich rocks andgarnet layers at P < 0·8 GPa. Progressive desiccationof retrogade fluids through crystallization of hydrous phasesled to a local formation of saline brines in the garnet layers.The presence of these brines resulted in a late-stage formationof Fe- and K-rich Ca-amphibole and Sr-rich apatite, both characterizedby extremely high Cl contents of up to 3·5 and 6·5wt % Cl, respectively. KEY WORDS: cumulates; Variscan metamorphism; SHRIMP dating; högbomite; saline brines     

Essexite occurrence in the Deccan volcanic province of Saurashtra,western India

The occurrence of essexite in the Deccan volcanic province of Saurashtra, India, is reported here for the first time. The essexite body occurs as a large stock-like intrusion in horizontal flow basalts. Petrographically it is characterized by the presence of titanaugite, labradorite, olivine, iron oxides and accessory amounts of alkali feldspar, analcite, biotite and apatite. Chemically it is characterized by enrichment in LILE, HFSE and REE as compared to the other tholeiitic and alkaline basalts of the area. It is therefore concluded that the essexite magma has not formed by differentiation out of the tholeiitic magma predominantly encountered in the Deccan volcanic province, but possibly represents a separate melt derived as a 5 to 10% partial melt at shallower depth (15 kb pressure) within the upper mantle.     

Fractional crystallization of primitive,hydrous arc magmas: an experimental study at 0.7 GPa

Differentiation of mantle-derived, hydrous, basaltic magmas is a fundamental process to produce evolved intermediate to SiO₂-rich magmas that form the bulk of the middle to shallow continental and island arc crust. This study reports the results of fractional crystallization experiments conducted in a piston cylinder apparatus at 0.7 GPa for hydrous, calc-alkaline to arc tholeiitic magmas. Fractional crystallization was approached by synthesis of starting materials representing the liquid composition of the previous, higher temperature experiment. Temperatures ranged from near-liquidus at 1,170 °C to near-solidus conditions at 700 °C. H₂O contents varied from 3.0 to more than 10 wt%. The liquid line of descent covers the entire compositional range from olivine–tholeiite (1,170 °C) to high-silica rhyolite (700 °C) and evolves from metaluminous to peraluminous compositions. The following crystallization sequence has been established: olivine → clinopyroxene → plagioclase, spinel → orthopyroxene, amphibole, titanomagnetite → apatite → quartz, biotite. Anorthite-rich plagioclase and spinel are responsible for a marked increase in SiO₂-content (from 51 to 53 wt%) at 1,040 °C. At lower temperatures, fractionation of amphibole, plagioclase and Fe–Ti oxide over a temperature interval of 280 °C drives the SiO₂ content continuously from 53 to 78 wt%. Largest crystallization steps were recorded around 1,040 °C and at 700 °C. About 40 % of ultramafic plutonic rocks have to crystallize to generate basaltic–andesitic liquids, and an additional 40 % of amphibole–gabbroic cumulate to produce granitic melts. Andesitic liquids with a liquidus temperature of 1,010 °C only crystallize 50 % over an 280 °C wide range to 730 °C implying that such liquids form mobile crystal mushes (<50 % crystals) in long-lived magmatic systems in the middle crust, allowing for extensive fractionation, assimilation and hybridization with periodic replenishment of more mafic magmas from deeper magma reservoirs.     

Magmatic Differentiation in the Uwekahuna Laccolith, Kilauea Caldera, Hawaii

Petrographic and chemicoal studies of a suite of rocks fromthe Uwekahuna laccolith of Kilauea Volcano show that the originalmafic tholeiitic magma differentiated into tholeiitic picrite,tholeiitic olivine gabbro, and an aphanitic rock approachingquartz-basalt in composition. Mechanisms involved were an initialgravity settling of olivine and a final filter pressing of theresidual liquid. The range of composition represented by therocks of the laccolith is as great as that found among all hithertoanalysed lavas of the volcano. ²Present address: U.S. Geological Survey, Menlo Park, California     

Metamorphic evolution of the coesite-bearing ultrahigh-pressure terrane in the North Qaidam, Northern Tibet, NW China

Widespread evidence for ultrahigh‐pressure (UHP) metamorphism is reported in the Dulan eclogite‐bearing terrane, the North Qaidam–Altun HP–UHP belt, northern Tibet. This includes: (1) coesite and associated UHP mineral inclusions in zircon separates from paragneiss and eclogite (identified by laser Raman spectroscopy); (2) inclusions of quartz pseudomorphs after coesite and polycrystalline K‐feldspar + quartz in eclogitic garnet and omphacite; and (3) densely oriented SiO₂ lamellae in omphacitic clinopyroxene. These lines of evidence demonstrate that the Dulan region is a UHP metamorphic terrane. In the North Dulan Belt (NDB), eclogites are characterized by the peak assemblage Grt + Omp + Rt + Phn + Coe (pseudomorph) and retrograde symplectites of Cpx + Ab and Hbl + Pl. The peak conditions of the NDB eclogites are P = 2.9–3.2 GPa, and T = 631–687 °C; the eclogite shows a near‐isothermal decompression P–T path suggesting a fast exhumation. In the South Dulan Belt (SDB), three metamorphic stages are recognized in eclogites: (1) a peak eclogite facies stage with the assemblage Grt + Omp + Ky + Rt + Phn at P = 2.9–3.3 GPa and T = 729–746 °C; (2) a high‐pressure granulite facies stage with Grt + Cpx (Jd < 30) + Pl (An24–29) + Scp at P = 1.9–2.0 GPa, T = 873–948 °C; and (3) an amphibolite facies stage with the assemblage Hbl + Pl + Ep/Czo at P = 0.7–0.9 GPa and T = 660–695 °C. The clockwise P–T path of the SDB eclogites is different from the near‐isothermal decompression P–T path from the NDB eclogites, which suggests that the SDB was exhumed to a stable crustal depth at a slower rate. In essence these two sub‐belts formed in different tectonic settings; they both subducted to mantle depths of around 100 km, but were exhumed to the Earth's surface separately along different paths. This UHP terrane plays an important role in understanding continental collision in north‐western China.     

Petrology of the Western Reykjanes Peninsula, Iceland

The active tholeiitic volcanic zone of the Reykjanes Peninsulaconsists of five volcanic fissure swarms, the two westernmostof which are the subject of this petrological study. The recent(less than 12,000 years) extrusives of the swarms group morphologicallyand petrographically into small picrite basalt lava shields,large olivine tholeiite lava shields and tholeiite fissure lavas;formed in that chronological succession. The picrite basalts exhibit a primitive mineralogy with chromite,olivine (Fo 89) and plagioclase (An 90) as phenocrysts and mayrepresent a primary liquid from the mantle. Simultaneous crystallizationof olivine, plagioclase and augite to form glomerocrysts inthe fissure lavas indicate low pressure cotectic crystallizationconditions. Twenty-eight new major element chemical analyses of the lavasare presented. They are generally characterized by a low contentof alkalies and high CaO. The lavas constitute two main suites,a lava shield suite and a fissure lava suite. There is a positivecorrelation between the volume of individual lavas and the contentof incompatible elements of the lavas within each group. Likewisethere is an overall chemical trend through time demonstrated,for example, by a rise in K₂O from about 0.02 per cent to 0.24per cent during the last, approximately, 12,000 years. There is an apparent chemical zoning within each volcanic swarmsuch that the most evolved and youngest lavas are found in thecentral axial area of the swarm. This central area is also characterizedby graben subsidence, high magnetic anomalies and high temperaturethermal areas, all indicative of shallow magma reservoir(s).In spite of indications of fractional crystallization in theevolution of the olivine tholeiites and tholeiites, some otherprocesses must be sought to explain the volume chemistry relations.Cyclic volcanic activity is tentatively suggested to explainthe observed regular temporal variations within the swarm, eachcycle starting with the formation of picrite basalts.