Shear Zone-hosted Migmatites (Eastern India): the Role of Dynamic Melting in the Generation of REE-depleted Felsic Melts, and Implications for Disequilibrium Melting

In the Ranmal migmatite complex, non-anatectic foliated graniteprotoliths can be traced to polyphase migmatites. Structural–microtexturalrelations and thermobarometry indicate that syn-deformationalsegregation–crystallization of in situ stromatic and diatexiteleucosomes occurred at 800°C and 8 kbar. The protolith,the neosome, and the mesosome comprise quartz, K-feldspar, plagioclase,hornblende, biotite, sphene, apatite, zircon, and ilmenite,but the modal mineralogy differs widely. The protolith compositionis straddled by element abundances in the leucosome and themesosome. The leucosomes are characterized by lower CaO, FeO+MgO,mg-number, TiO₂ , P₂O₅ , Rb, Zr and total rare earth elements(REE), and higher SiO₂ , K₂O, Ba and Sr than the protolith andthe mesosome, whereas Na₂O and Al₂O₃ abundances are similar.The protolith and the mesosome have negative Eu anomalies, butprotolith-normalized abundances of REE-depleted leucosomes showpositive Eu anomalies. The congruent melting reaction for leucosomeproduction is inferred to be 0·325 quartz+0·288K-feldspar+0·32 plagioclase+0·05 biotite+0·014hornblende+0·001 apatite+0·001 zircon+0·002sphene=melt. Based on the reaction, large ion lithophile element,REE and Zr abundances in model melts computed using dynamicmelting approached the measured element abundances in leucosomesfor >0·5 mass fraction of unsegregated melts withinthe mesosome. Disequilibrium-accommodated dynamic melting andequilibrium crystallization of melts led to uniform plagioclasecomposition in migmatites and REE depletion in leucosome. KEY WORDS: migmatite; REE; trace element; partial melting; P–T conditions     

Formation of Diatexite Migmatite and Granite Magma during Anatexis of Semi-pelitic Metasedimentary Rocks: an Example from St. Malo, France

Petrological and geochemical variations are used to investigatethe formation of granite magma from diatexite migmatites derivedfrom metasedimentary rocks of pelitic to greywacke compositionat St. Malo, France. Anatexis occurred at relatively low temperaturesand pressures (<800°C, 4–7 kbar), principally throughmuscovite dehydration melting. Biotite remained stable and servesas a tracer for the solid fraction during melt segregation.The degree of partial melting, calculated from modal mineralogyand reaction stoichiometry, was <40 vol. %. There is a continuousvariation in texture, mineralogy and chemical composition inthe diatexite migmatites. Mesocratic diatexite formed when metasedimentaryrocks melted sufficiently to undergo bulk flow or magma flow,but did not experience significant melt–residuum separation.Mesocratic diatexite that underwent melt segregation duringflow generated (1) melanocratic diatexites at the places wherethe melt fraction was removed, leaving behind a biotite andplagioclase residuum (enriched in TiO₂, FeO_T, MgO, CaO, Sc,Ni, Cr, V, Zr, Hf, Th, U and REE), and (2) a complementary leucocraticdiatexite (enriched in SiO₂, K₂O and Rb) where the melt fractionaccumulated. Leucocratic diatexite still contained 5–15vol. % residual biotite (mg-number 40–44) and 10–20vol. % residual plagioclase (An₂₂). Anatectic granite magmadeveloped from the leucodiatexite, first by further melt–residuumseparation, then through fractional crystallization. Most biotitein the anatectic granite is magmatic (mg-number 18–22). KEY WORDS: anatexis; diatexite; granite magma; melt segregation; migmatite     

Effects of P, f(O2) and Mg/Fe Ratio on Dehydration Melting of Model Metagreywackes

We present results of dehydration melting experiments [3–15kbar, 810–950C f(O₂) QFM (quartz-fayalite-magetite)and Ni-NiO] on two Fe-rich mixtures of biotite (37%), plagioclaseAn₃₈ (27%), quartz (34%) and ilmenite (2%), which differ onlyin their biotite compositions (mg-number 23 and 0.4). Dehydrationmelting of metagreywackes of constant modal composition generatesa wide range of melt fractions, melt compositions and residualassemblages, through the combined effects of pressure, Fe/Mgratio and f(O₂). Crystallization of garnet is the chief controlon melting behavior, and is limited by two reactions: (1) thebreakdown of garnet + quartz to orthopyroxene + plagioclaseat low P, and (2) the oxidation of garnet to magnetite + anorthite+ quartz (enstatite), which is sensitive to both f(O₂) andP. Because of these reactions, melting of Mg-rich metagreywackesis rather insensitive to f(O₂) but strongly sensitive to P;the converse is true for Fe-rich metagreywackes. Garnet crystallizationrequires that plagioclase break down incongruently, liberatingalbite. This increases the Na₂O content of the melts and enhancesmelt production. Thus, melting of metagreywacke in a reducingdeep-crustal environment (with garnet stable) would producemore, and more sodic, melt than would garnet-absent meltingof the same source material in a relatively oxidizing, shallow-crustalenvironment. KEY WORDS: anatexis; metasediments; gneisses; granites; garnet ^*Corresponding author. Telephone: 706-542-2394; fax: 706-542-2425; e-mail: alpatino{at}uga.cc.uga.edu     

Disequilibrium Melting and the Rate of Melt-Residuum Separation During Migmatization of Mafic Rocks from the Grenville Front, Quebec

Migmatites are developed in Archaean metabasites south of theGrenville Front. Relative to equivalent greenschist facies metabasites,those hosting the migmatites have undergone some mobilizationof CaO, Na₂O, and Sr, and, in the case of sheared metabasites,the introduction of K₂O, Ba, Cs, and Rb, before migmatization.Three types of anatectic migmatite are recognized, based ontheir leucosome-melanosome relationships: (1) non-segregatedmigmatites in which new leucocratic and magic phases are intimatelymixed in patches up to 15 cm across, (2) segregated migmatitesin which the leucosomes are located in boudin necks and shearbands, and are separated from their associated mafic selvedgesby 5–100 cm, and (3) vein-type migmatites where discordantleucosomes lack mafic selvedges. The non-segregated and segregatedmigmatites have a local and essentially isochemical origin,whereas the vein-type represent injected melt. Leucosomes fromthe segregated and vein-type migmatites have similar tonaliticmajor oxide compositions, but they differ greatly in their trace-elementcharacteristics. The vein-type leucosomes are enriched in K₂O, Ba, Cs, Rb, LREE,Th, Hf, Zr, and P2O5 relative to their metabasite hosts, andhave greater La/Yb_N ratios (27 compared with 0?6–17).These veins may have formed by between 5 and 25%equilibriumbatch partial melting of Archaean metabasalt, leaving garnet+ hornblende in the residuum. In contrast, leucosomes from the segregated migmatites are depletedin REE, Sc, V, Cr, Ni, Co, Ti, Th, Hf, Zr, Nb, and P₂O₅ relativeto their source rocks; the associated mafic selvedges are enrichedin these elements. The leucosomes and mafic selvedges both haveLa/Yb_N ratios that are similar to those of the source metabasitesirrespective of whether the source is LREE depleted or LREEenriched. The abundances of many trace elements in the leucosomesappear to be controlled by the degree of contamination withresiduum material. Zr concentrations in the leucosomes are between10 and 52% of the estimated equilibrium concentrations in felsicmelts at the temperature (750–775 ?C) of migmatization.A numerical simulation of disequilibrium melting using bothLREE-depleted and LREE-enriched sources yields model melts withtrace element abundances that match those of the natural leucosomes.Mafic selvedge compositions indicate that the segregated migmatitesrepresent a range of between 12 and 36% partial melting of theirhost metamatization. Based upon calculated dissolution times for zircon in wet melts,the melt and residuum were separated in less than 23a, otherwisemelts would have become saturated in Zr. Rapid melt extractionis thought to be driven by pressure gradients developed duringnon-coaxial deformation of the anisotropic palaeosome duringmigmatization. The common occurrence, based on published work, of disequilibriumcompositions in migmatite leucosomes implies that during mid-crustalmelting the melt-segregation rates are greater than the rateof chemical equilibration between melt and the residual solid.In contrast, at the higher temperatures of granite formation,the rate of chemical equilibration exceeds that of melt-segregationand equilibrium melt compositions are reached before segregationcan occur. On the basis of their trace element characteristics,the melt which forms segregated migmatites cannot be the sameas that which forms the vein-like migmatites, or granitoid plutons.     

Formation, Crystallization, and Migration of Melt in the Mid-orogenic Crust: Muskoka Domain Migmatites, Grenville Province, Ontario

Migmatitic orthogneisses in the Muskoka domain, southwesternGrenville Province, Ontario, formed during the Ottawan stage(c. 1080–1050 Ma) of the Grenvillian orogeny. Stromaticmigmatites are volumetrically dominant, comprising granodioriticgneisses with 2–5 cm thick granitic leucosomes, locallyrimmed by thin melanosomes, that constitute 20–30 vol.%, and locally 40–50 vol. %, of the outcrops. Patch migmatitesin dioritic gneisses form large (>10 m) pinch-and-swell structureswithin the stromatic migmatites, and consist of decimetre-scale,irregular patches of granitic leucosome, surrounded by medium-grainedhornblende–plagioclase melanosomes interpreted as restite.The patches connect to larger networks of zoned pegmatite dykes.Petrographic and geochemical evidence suggests that the patchleucosomes formed by 20–40% fluid-present, equilibriummelting of the dioritic gneiss, followed by feldspar-dominatedcrystallization. The dyke networks may have resulted from hydraulicfracturing, probably when the melts reached water saturationduring crystallization. Field and geochemical data from thestromatic migmatites suggest a similar petrogenesis to the patchmigmatites, but with significant additions of externally derivedmelts, indicating that they acted as conduits for melts derivedfrom deeper structural levels within the orogen. We hypothesizethat the Muskoka domain represents a transfer zone for meltsmigrating to higher structural levels during Grenvillian deformation. KEY WORDS: migmatite geochemistry; partial melting; melt crystallization; melt transport; Grenville orogen     

Melting of Biotite + Plagioclase + Quartz Gneisses: the Role of H2O in the Stability of Amphibole

Biotite + plagioclase + quartz (BPQ) is a common assemblagein gneisses, metasediments and metamorphosed granitic to granodioriticintrusions. Melting experiments on an assemblage consistingof 24 vol. % quartz, 25 vol. % biotite (XMg = 0·38–0·40),42 vol. % plagioclase (An_26–29), 9 vol. % alkali feldsparand minor apatite, titanite and epidote were conducted at 10,15 and 20 kbar between 800 and 900°C under fluid-absentconditions and with small amounts (2 and 4 wt %) of water addedto the system. At 10 kbar when 4 wt % of water was added tothe system the biotite melting reaction occurred below 800°Cand produced garnet + amphibole + melt. At 15 kbar the meltingreaction produced garnet + amphibole + melt with 2 wt % addedwater. At 20 kbar the amphibole occurred only at high temperature(900°C) and with 4 wt % added water. In this last case themelting reaction produced amphibole + clinopyroxene ±garnet + melt. Under fluid-absent conditions the melting reactionproduced garnet + plagioclase II + melt and left behind a plagioclaseI ± quartz residuum, with an increase in the modal amountof garnet with increasing pressure. The results show that itis not possible to generate hornblende in such compositionswithout the addition of at least 2–4 wt % H₂O. This reflectsthe fact that conditions of low aH₂O may prevent hornblendefrom being produced with peraluminous granitic liquids fromthe melting of biotite gneiss. Thus growth of hornblende inanatectic BPQ gneisses is an indication of addition of externalH₂O-rich fluids during the partial melting event. KEY WORDS: biotite; dehydration; gneisses; hornblende; melt     

Synthesis of Staurolite in Melting Experiments of a Natural Metapelite: Consequences for the Phase Relations in Low-Temperature Pelitic Migmatites

We document experiments on a natural metapelite in the range650–775°C, 6–14 kbar, 10 wt % of added water,and 700–850°C, 4–10 kbar, no added water. Staurolitesystematically formed in the fluid-present melting experimentsabove 675°C, but formed only sporadically in the fluid-absentmelting experiments. The analysis of textures, phase assemblages,and variation of phase composition and Fe–Mg partitioningwith P and T suggests that supersolidus staurolite formed at(near-) equilibrium during fluid-present melting reactions.The experimental results are used to work out the phase relationsin the system K₂O–Na₂O–FeO–MgO–Al₂O₃–SiO₂–H₂Oappropriate for initial melting of metapelites at the upperamphibolite facies. The P–T grid developed predicts theexistence of a stable P–T field for supersolidus staurolitethat should be encountered by aluminous Fe-rich metapelitesduring fluid-present melting at relatively low temperature andintermediate pressures (675–700°C, 6–10 kbarfor X_H2O = 1, in the KNFMASH system), but not during fluid-absentmelting. The implications of these findings for the scarcityof staurolite in migmatites are discussed. KEY WORDS: metapelites; migmatites; partial melting; P–T grid; staurolite     

Records of Crustal Metasomatism in the Garnet Peridotites of the Ulten Zone (Upper Austroalpine, Eastern Alps)

Peridotites in the Ulten Zone (Upper Austroalpine, Eastern Alps),occur as small bodies within lower-crustal rocks (gneisses andmigmatites) subducted at eclogite-facies conditions during theVariscan orogeny. They record a complex metamorphic and deformationevolution as indicated by the transition from coarse-grainedspinel-bearing peridotites to fine-grained garnet + amphibole-bearingperidotites, and are interpreted as portions of mantle wedgethat were incorporated in a downgoing slab of cold continentalcrust. The transition from spinel- to garnet-bearing assemblagewas accompanied by significant input of metasomatic agents,as shown by the crystallization of abundant amphibole. Herewe present trace-element mineral chemistry data for selectedUlten peridotites, with the aim of unravelling the nature ofthe metasomatic processes. Amphiboles display significant lightrare earth element (LREE) enrichment [Ce_N/Yb_N = 3·90–11·50;LREE up to (20–50) x C1], high Sr (150–250 ppm),K (1910–7280 ppm) and Ba (280–800 ppm) contents,and low concentrations of high field strength elements (HFSE)(Zr = 14–25 ppm, Y = 6·7–16 ppm, Ti = 1150–2500ppm, Nb = 2–7 ppm). On the basis of (1) the evidence formodal orthopyroxene decrease as a result of the garnet-formingreaction rather than abundant orthopyroxene crystallization,(2) the high modal amounts of amphibole (up to 23%) in the mostmetasomatized peridotites and (3) the strong large ion lithophileelement (LILE)/HFSE fractionation in amphiboles, we infer thatthe metasomatic agent was an H₂O–CO₂ fluid with a lowCO₂/H₂O ratio. Petrological investigations and geochronologicaldata indicate that the host metapelites experienced in situpartial melting and migmatization concomitantly with the garnet+ amphibole-facies recrystallization in the enclosed peridotites.We infer that the metasomatizing hydrous fluids could representthe residual fluids left after the crystallization of leucosomes,starting from water-undersaturated melts produced during migmatizationof the host gneisses. KEY WORDS: garnet peridotite; crustal metasomatism; amphibole; hydrous fluids     

High-Pressure Dehydration Melting of Metapelites: Evidence from the Migmatites of Yaounde (Cameroon)

The migmatites of Yaound? consist essentially of anatectic metapelitickyanite-garnet gneisses characterized by granulite-facies mineralassemblages. Several types of migmatitic rocks have been recognized:(1) leucosomes associated with garnet-rich melanosomes, conformablewith the regional metamorphic layering; some leucosomes aregranitic in composition whereas some others are granodioriticand characterized by low K and Rb and by the lack of HREE fractionation;(2) quartzo-feldspathic differentiations without the relatedmelanosomes, occurring as veins conformable with or cross-cuttingthe regional metamorphic layering or along shear-zones, andcorresponding mineralogi-cally to granitic or quartz-rich v?ins;(3) garnet-rocks mainly composed of garnet with abundant accessories,occurring as intrusive bodies within the migmatitic series. Structural and petrographic data suggest that the migmatitesare not derived from the surrounding granulite-facies gneissesbut that both types of rock result from a single dehydrationmelting event. The formation of migmatites or gneisses, interpretedin terms either of absence of melt extraction or of shear-inducedmelt segregation, is ascribed to variations in strain distributionwithin the metamorphic pile. The chemical characteristics of the rocks and petrogenetic modellingsuggest that the migmatites of Yaounde arose from the superimpositionof the following events: (1) subsolidus differentiation of biotite-gneisses;(2) dehydration melting of biotite-gneisses at temperaturesaround 800?C (P=10–12 kbX leading to low amounts of melt(F<0?2), which was either tectonically segregated (migmatites)or not (granulite-facies gneisses); (3) injection of anatecticmaterial comprising both partial melts and garnet-rich residues,corresponding to high melt fractions (F>0?5) and probablyformed at higher temperatures (850?C) and at deeper structurallevels. The REE signature of equilibrium partial melts (9?3<Ce_N/Yb_N78;l?2<Yb_N<5?4) indicates that granitic magmas cannot bederived from dehydration melting of biotite-bearing metapelitesonly. Several other possibilities are discussed.     

Calculation of Phase Relations Involving Haplogranitic Melts Using an Internally Consistent Thermodynamic Dataset

A simple thermodynamic model is developed for silicate meltsin the system CaO–Na₂O–K₂O–Al₂O₃–SiO₂–H₂O(CNKASH). The Holland & Powell (Journal of Metamorphic Geology,16, 289–302, 1998) internally consistent thermodynamicdataset is extended via the incorporation of the experimentallydetermined melting relationships in unary and binary subsystemsof CNKASH. The predictive capability of the model is evaluatedvia the experimental data in ternary and quaternary subsystems.The resulting dataset, with the software THERMOCALC, is thenused to calculate melting relationships for haplogranitic compositions.Predictions of the P–T stabilities of assemblages in water-saturatedand -undersaturated bulk compositions are illustrated. It isnow possible to make useful calculations of the melting behaviourof appropriate composition rocks under crustal conditions. KEY WORDS: thermodynamics; melts; granite; dataset     

Melting Behaviour of Model Lherzolite in the System CaO-MgO-Al2O3-SiO2-FeO at 0{middle dot}7-2{middle dot}8 GPa

Fe–Mg exchange is the most important solid solution involvedin partial melting of spinel lherzolite, and the system CaO–MgO–Al₂O₃–SiO₂–FeO(CMASF) is ideally suited to explore this type of exchange duringmantle melting. Also, if primary mid-ocean ridge basalts arelargely generated in the spinel lherzolite stability field bynear-fractional fusion, then Na and other highly incompatibleelements will early on become depleted in the source, and themelting behaviour of mantle lherzolite should resemble the meltingbehaviour of simplified lherzolite in the CMASF system. We havedetermined the isobarically univariant melting relations ofthe lherzolite phase assemblage in the CMASF system in the 0·7–2·8GPa pressure range. Isobarically, for every 1 wt % increasein the FeO content of the melt in equilibrium with the lherzolitephase assemblage, the equilibrium temperature is lower by about3–5°C. Relative to the solidus of model lherzolitein the CaO–MgO–Al₂O₃–SiO₂ system, melt compositionsin the CMASF system are displaced slightly towards the alkalicside of the basalt tetrahedron. The transition on the solidusfrom spinel to plagioclase lherzolite has a positive Clapeyronslope with the spinel lherzolite assemblage on the high-temperatureside, and has an almost identical position in P–T spaceto the comparable transition in the CaO–MgO–Al₂O₃–SiO₂–Na₂O(CMASN) system. When the compositions of all phases are describedmathematically and used to model the generation of primary basalts,temperature and melt composition changes are small as percentmelting increases. More specifically, 10% melting takes placeover 1·5–2°C, melt compositions are relativelyinsensitive to the degree of melting and bulk composition, andequilibrium and near-fractional melting yield similar melt compositions.FeO and MgO are the oxides that exhibit the greatest changein the melt with degree of melting and bulk composition. Theamount of FeO decreases with increasing degree of melting, whereasthe amount of MgO increases. The coefficients for Fe–Mgexchange between the coexisting crystalline phases and melt,K_dFe–Mg^xl–liq, show a relatively simple and predictablebehaviour with pressure and temperature: the coefficients forolivine and spinel do not show significant dependence on temperature,whereas the coefficients for orthopyroxene and clinopyroxeneincrease with pressure and temperature. When melting of lherzoliteis modeled in the CMASF system, a strong linear correlationis observed between the mg-number of the lherzolite and themg-number of the near-solidus melts. Comparison with meltingin the CMASN system indicates that Na₂O has a strong effecton lherzolite melting behaviour only at small degrees of melting. KEY WORDS: CMASF; lherzolite solidus; mantle melting     

Volatiles in Basaltic Glasses from Loihi Seamount, Hawaii: Evidence for a Relatively Dry Plume Component

New H₂O, CO₂ and S concentration data for basaltic glasses fromLoihi seamount, Hawaii, allow us to model degassing, assimilation,and the distribution of major volatiles within and around theHawaiian plume. Degassing and assimilation have affected CO₂and Cl but not H₂O concentrations in most Loihi glasses. Waterconcentrations relative to similarly incompatible elements inHawaiian submarine magmas are depleted (Loihi), equivalent (Kilauea,North Arch, Kauai–Oahu), or enriched (South Arch). H₂O/Ceratios are uncorrelated with major element composition or extentor depth of melting, but are related to position relative tothe Hawaiian plume and mantle source region composition, consistentwith a zoned plume model. In front of the plume core, overlyingmantle is metasomatized by hydrous partial melts derived fromthe Hawaiian plume. Downstream from the plume core, lavas tapa depleted source region with H₂O/Ce similar to enriched Pacificmid-ocean ridge basalt. Within the plume core, mantle components,thought to represent subducted oceanic lithosphere, have waterenrichments equivalent to (KEA) or less than (KOO) that of Ce.Lower H₂O/Ce in the KOO component may reflect efficient dehydrationof the subducting oceanic crust and sediments during recyclinginto the deep mantle. KEY WORDS: basalt; Hawaii; mantle; plumes; volatiles     

Geochemical Constraints on Leucogranite Magmatism in the Langtang Valley, Nepal Himalaya

A complex of crustally derived leucogranitic sills emplacedinto sillimanite-grade psammites in the upper Langtang Valleyof northern Nepal forms part of the Miocene High Himalayan graniteassociation. A series of post-tectonic, subvertical leucograniticdykes intrude the underlying migmatites, providing possiblefeeders to the main granite sills. The leucogranite is peraluminous and alkali-rich, and can besubdivided into a muscovite–biotite and a tourmaline–muscovitefacies. Phase relations suggest that the tourmaline leucogranitescrystallized from a water-undersaturated magma of minimum-meltcomposition at pressures around 3–4 kbar. Potential metasedimentaryprotoliths include a substantial anatectic migmatite complexand a lower-grade mica schist sequence. Isotopic constraintspreclude the migmatites as a source of the granitic melts, whereastrace-element modelling of LILEs (Rb, Sr, and Ba), togetherwith the Nd and Sr isotopic signatures of potential protoliths,strongly suggest that the tourmaline-bearing leucogranites havebeen generated by fluid-absent partial melting of the muscovite-richschists. However, REE and HFSE distributions cannot be reconciledwith equilibrium melting from such a source. Systematic covariationsbetween Rb, Sr, and Ba can be explained by variations in protolithmineralogy and P–T–a_H2O. Tourmaline leucogranites with high Rb/Sr ratios represent low-fraction-melts(F{small tilde} 12%) efficiently extracted from their protolithsunder conditions of low water activity, whereas the heterogeneoustwo-mica granites may result from melting under somewhat highera_H2O conditions. The segregation of low-degree melts from sourcewas probably by deformation-enhanced intergranular flow andmagma fracturing, with the mechanisms of migration and emplacementcontrolled by variations in the uppercrustal stress regime duringlate–orogenic extensional collapse of the thickened crust.     

Large-scale melt-depletion in granulite terranes: an example from the Archean Ashuanipi Subprovince of Quebec

This study uses field, petrographic and geochemical methods to estimate how much granitic melt was formed and extracted from a granulite facies terrane, and to determine what the grain‐ and outcrop‐scale melt‐flow paths were during the melt segregation process. The Ashuanipi subprovince, located in the north‐eastern Superior Province of Quebec, is a large (90 000 km²) metasedimentary terrane, in which > 85% of the metasediments are of metagreywacke composition, that was metamorphosed at mid‐crustal conditions (820–900 °C and 6–7 kbar) in a late Archean dextral, transpressive orogen. Decrease in modal biotite and quartz as orthopyroxene and plagioclase contents increase, together with preserved former melt textures indicate that anatexis was by the biotite dehydration reaction: biotite + quartz + plagioclase = melt + orthopyroxene + oxides. Using melt/orthopyroxene ratios for this reaction derived from experimental studies, the modal orthopyroxene contents indicate that the metagreywacke rocks underwent an average of 31 vol% partial melting. The metagreywackes are enriched in MgO, CaO and FeO_t and depleted in SiO₂, K₂O, Rb, Cs, and U, have lower Rb/Sr, higher Rb/Cs and Th/U ratios and positive Eu anomalies compared to their likely protolith. These compositions are modelled by the extraction of between 20 and 40 wt %, granitic melt from typical Archean low‐grade metagreywackes. A simple mass balance indicates that about 640 000 km³ of granitic melt was extracted from the depleted granulites. The distribution of relict melt at thin section‐ and outcrop‐scales indicates that in layers without leucosomes melt extraction occurred by a pervasive grain boundary (porous) flow from the site of melting, across the layers and into bedding planes between adjacent layers. In other rocks pervasive grain boundary flow of melt occurred along the layers for a few, to tens of centimetres followed by channelled flow of melt in a network of short interconnected and structurally controlled conduits, visible as the net‐like array of leucosomes in some outcrops. The leucosomes contain very little residual material (< 5% biotite + orthopyroxene) indicating that the melt fraction was well separated from the residuum left in situ as melt‐depleted granulite. Only 1–3 vol percentage melt remained in the melt‐depleted granulites, hence, the extraction of melt generated by biotite dehydration melting in these granulites, was virtually complete under conditions of natural melting and strain rates in a contractional orogen.     

Volatile Components, Magmas, and Critical Fluids in Upwelling Mantle

The phase diagram for lherzolite–CO₂–H₂O providesa framework for interpreting the distribution of phase assemblagesin the upper mantle with various thermal structures, in differenttectonic settings. Experiments show that at depths >80 km,the near-solidus partial melts from lherzolite–CO₂–H₂Oare dolomitic, changing through carbonate–silicate liquidswith rising temperatures to mafic liquids; vapor, if it coexists,is aqueous. Experimental data from simple systems suggest thata critical end-point (K) occurs on the mantle solidus at anundetermined depth. Isobaric (T–X) phase diagrams forvolatile-bearing systems with K elucidate the contrasting phaserelationships for lherzolite–CO₂–H₂O at depths belowand above a critical end-point, arbitrarily placed at 250 km.At levels deeper than K, lherzolite can exist with dolomiticmelt, aqueous vapor, or with critical fluids varying continuouslybetween these end-members. Analyses of fluids in microinclusionsof fibrous diamonds reveal this same range of compositions,supporting the occurrence of a critical end-point. Other evidencefrom diamonds indicates that the minimum depth for this end-pointis 125 km; maximum depth is not constrained. Constructed cross-sectionsshowing diagrammatically the phase fields intersected by upwellingmantle indicate how rising trace melts may influence trace elementconcentrations within a mantle plume. KEY WORDS: mantle solidus; critical end-point; dolomitic magma; diamond inclusions; critical fluids     

Mantle Xenoliths from Tenerife (Canary Islands): Evidence for Reactions between Mantle Peridotites and Silicic Carbonatite Melts inducing Ca Metasomatism

Mantle xenoliths from Tenerife show evidence of metasomatismand recrystallization overprinting the effects of extensivepartial melting. The evidence includes: recrystallization ofexsolved orthopyroxene porphyroclasts highly depleted in incompatibletrace elements into incompatible-trace-element-enriched, poikiliticorthopyroxene with no visible exsolution lamellae; formationof olivine and REE–Cr-rich, strongly Zr–Hf–Ti-depletedclinopyroxene at the expense of orthopyroxene; the presenceof phlogopite; whole-rock CaO/Al₂O₃ >> 1 (Ca metasomatism) inrecrystallized rocks; and enrichment in incompatible elementsin recrystallized rocks, relative to rocks showing little evidenceof recrystallization. The ‘higher-than-normal’ degreeof partial melting that preceded the metasomatism probably resultsfrom plume activity during the opening of the Central AtlanticOcean. Sr–Nd isotopic compositions are closely similarto those of Tenerife basalts, indicating resetting from theexpected original mid-ocean ridge basalt composition by themetasomatizing fluids. Metasomatism was caused by silicic carbonatitemelts, and involved open-system processes, such as trappingof elements compatible with newly formed acceptor minerals,leaving residual fluids moving to shallower levels. The compositionsof the metasomatizing fluids changed with time, probably asa result of changing compositions of the melts produced in theCanary Islands plume. Spinel dunites and wehrlites representrocks where all, or most, orthopyroxene has been consumed throughthe metasomatic reactions. KEY WORDS: Canary Islands; Tenerife; mantle xenoliths; geochemistry; Ca metasomatism; open-system processes; lithosphere; ocean islands     

Granulite Metamorphism, Fluid Buffering, and Dehydration Melting in the Madras Charnockites and Metapelites

Interlayered and cofolded charnockites and metapelites of thetype charnockite area near Madras were metamorphosed under granulitefades conditions. Fe-Mg partitioning between orthopyroxene,garnet, and biotite indicates that chemical equilibrium wasapproached under similar P-T conditions in the two rock suites.Several geothennometers and geobarometers give P-T values whichconverge at 750–800?C and 6.5–7.5 kb. Computations utilizing data from high pressure phase equilibriumexperiments of Bohlen et al. (1983a) and Wones & Dodge (1977)point to several significant relations regarding the behaviourof H₂O during the granulite metamorphism. a_H2O values, computedfrom Bohlen et al.'s (1983a) reversal data and the a-X modelfor phlogopite after Bohlen et al. (1980), show distinctly lowermagnitudes in metapelites (0.10–0.16) than in charnockites(0.23–0.34). No systematic spatial gradients exist withinthe charnockites or metapelites, and a_H2O has similar valuesin metapelite exposures widely separated in the field. Theseimply an internal, rather than an external (e.g., by CO2 influx),control of the fluids. Applying the algebraic method developed by Rumble (1976), Gibbsanalysis in the system K₂O-MgO-FeO-Fe₂O₃-Al₂O₃-SiO₂-TiO₂-H₂Oshows that the chemical potentials of H₂O and to O₂, as monitoredagainst biotite composition and , exhibit gradients with respect to X_Mg in the two rock suites under isothermal-isobaricconditions. µ_H2O was found to decrease with X_Mg^bt in both,while µ_O2 increases with decreasing X_Mg^bt in metapelitesbut increases sympathetically with X_Mg^bt in charnockites. Thesefindings point out again that µ_H2O and µ_O2 wereinternally buffered. The absence of graphite in the metapelites,at an estimated f_O2 = 10^–14.7 b, also argues against anexternal influx of CO₂ and, inter alia, supports internal buffering.A complementary enquiry into variations of a_TIO2 reveals aninverse relation between a_TIO2 and a_H2O, suggesting a similarcontrol for a_TIO2. The inferences from biotite dehydration equilibria, when combinedwith the P-T data and with several field and chemical featuresof these rocks noted earlier (Sen, 1974), make dehydration meltinga distinct possibility for the Madras rocks. It is argued thatthe low a_H2O and high a_TIO2 ({small tilde} 0.9) observed inthe metapelites have been caused by a greater extent of meltingin the precursors of metapelites, which were more hydrous thanthose of charnockites, coupled with preferential partitioningof Ti into the residual rocks—thus strengthening the casefor dehydration melting.     

Water-Saturated and -Undersaturated Melting of Metaluminous and Peraluminous Crustal Compositions at 10 kb: Evidence for the Origin of Silicic Magmas in the Taupo Volcanic Zone, New Zealand, and Other Occurrences

The melting relations of two proposed crustal source compositionsfor rhyolitic magmas of the Taupo Volcanic Zone (TVZ), New Zealand,have been studied in a piston-cylinder apparatus at 10 kb totalpressure and a range of water activities generated by H₂O-CO₂vapour. Starting materials were glasses of intermediate composition(65 wt.% Si0₂ representing a metaluminous ‘I-type’dacite and a peraluminous ‘S-type’ greywacke. Crystallizationexperiments were carried out over the temperature range 675to 975?C, with aH₂O values of approximately 1?0, 0?75, 0?5,and 0?25. Talc-pyrex furnace assemblies imposed oxygen fugacitiesclose to quartz-fayalite-magnetite buffer conditions. Assemblages in both compositions remain saturated with quartzand plagioclase through 675–700?C at high aH₂O, 725–750?Cat aH₂O0?5, and 800–875?C at aH₂O0?25, corresponding to<60–70% melting. Concentrations of refractory mineralcomponents (Fe, Mg, Mn, P, Ti) in liquids increase throughoutthis melting interval with increasing temperature and decreasingaH₂O. Biotite and hornblende are the only mafic phases presentnear the solidus in the dacite, compared with biotite, garnet,gedritic orthoamphibole, and tschermakitic clinoamphibole inthe greywacke. Near-solidus melting reactions are of the type:biotite + quartz + plagioclase = amphibole ? garnet, potentiallyreleasing H₂O for dehydration melting in the greywacke, butproducing larger amounts of hornblende and releasing littleH₂O in the dacite. At aH₂O0?25 and temperatures 825–850?C,amphibole dehydration produces anhydrous mineral phases typicalof granulite fades assemblages (clinopyroxene, orthopyroxene,plagioclase?quartz in the dacite; garnet, orthopyroxene, plagioclase?quartzin the greywacke) coexisting with melt proportions as low as40%. Hornblendce-saturated liquids in the dacite are weaklyperaluminous (0?3–1?6 wt.% normative C—within therange of peraluminous TVZ rhyolites), whereas, at aH₂O0?25 andtemperatures 925?C, metaluminous partial melt compositions (upto 1?8 wt.% normative Di) coexist with plagioclase, orthopyroxene,and clinopyroxene. At all water activities, partial melts ofthe greywacke are uniformly more peraluminous (1?5–2?6wt.% normative C), reflecting their saturation in the componentsof more aluminous mafic minerals, particularly garnet and Al-richorthopyroxene. A metaluminous source for the predominantly Di-normativeTVZ rhyolites is therefore indicated. With decreasing aH₂O the stability fields of plagioclase andquartz expand, whereas that of biotite contracts. These changesare reflected in the proportions of normative salic componentsin partial melts of both the dacite and greywacke. At high aH₂O,partial melts are rich in An and Ab and poor in Or (trondhjemitic-tonalitic);with decreasing aH₂O they become notably poorer in An and richerin Or (granodioritic-granitic). These systematic variationsin salic components observed in experimental metaluminous tostrongly peraluminous melts demonstrate that a wide varietyof granitoid magmas may be produced from similar source rocksdepending upon P-T-aH₂O conditions attending partial melting.Some peraluminous granitoids, notably trondhjemitic leucosomesin migmatites, and sodic granodiorites and granites emplacedat deep crustal levels, have bulk compositions similar to nearsolidus melt compositions in both the dacite and greywacke,indicating possible derivation by anatexis without the involvementof a significant restite component.     

Petrogenesis of a Stromatic Migmatite (Nelaug, Southern Norway)

The stromatic migmatites of Nelaug (Tvedestrand area, SouthernNorway) are investigated in detail. They show well developedlayers of leucosomes, mesosomes and melanosomes. It is establishedthat the mesosomes and leucosomes of these migmatites are differentfrom each other texturally, mineralogically, and chemically.Also combinations of leucosome plus adjacent melanosome portionsare chemically different from those of the mesosomes. Theseobservations do not agree with the findings of Mehnert (1971)and do not fit into his genetic model. The mesosome layers and the leucosome + melanosome combinationsare taken to represent the chemical compositions of the countryrock, a metagraywacke with relicts of primary rhythmic layering(Touret, 1965). The mineralogical composition of the layersvaries from granitic to tonalitic. Relict textures indicatethat the leucosome portions were initially occupied by layersof granitic composition relatively rich in K-feldspar, whereasthe mesosomes are the representatives of those metagraywackelayers which were relatively rich in plagioclase. An almostisochemical transformation of a paragneiss into the investigatedstromatic migmatite is established. Melting experiments performed at PH₂O= 5 Kb yielded solidustemperatures of 640±7 °C for all layers. The Composition of plagioclases present in the different layersis explained by isochemical partial melting and in situ crystallization.The chemical, mineralogical, and textural findings support themodel of almost isochemical transformation already establishedfor the Arvika migmatites (Johannes & Gupta, 1982).     

Melting of Amphibole-bearing Wehrlites: an Experimental Study on the Origin of Ultra-calcic Nepheline-normative Melts

Olivine + clinopyroxene ± amphibole cumulates have beenwidely documented in island arc settings and may constitutea significant portion of the lowermost arc crust. Because ofthe low melting temperature of amphibole (1100°C), suchcumulates could melt during intrusion of primary mantle magmas.We have experimentally (piston-cylinder, 0·5–1·0GPa, 1200–1350°C, Pt–graphite capsules) investigatedthe melting behaviour of a model amphibole–olivine–clinopyroxenerock, to assess the possible role of such cumulates in islandarc magma genesis. Initial melts are controlled by pargasiticamphibole breakdown, are strongly nepheline-normative and areAl₂O₃-rich. With increasing melt fraction (T > 1190°Cat 1·0 GPa), the melts become ultra-calcic while remainingstrongly nepheline-normative, and are saturated with olivineand clinopyroxene. The experimental melts have strong compositionalsimilarities to natural nepheline-normative ultra-calcic meltinclusions and lavas exclusively found in arc settings. Theexperimentally derived phase relations show that such naturalmelt compositions originate by melting according to the reactionamphibole + clinopyroxene = melt + olivine in the arc crust.Pargasitic amphibole is the key phase in this process, as itlowers melting temperatures and imposes the nepheline-normativesignature. Ultra-calcic nepheline-normative melt inclusionsare tracers of magma–rock interaction (assimilative recycling)in the arc crust. KEY WORDS: experimental melting; subduction zone; ultra-calcic melts; wehrlite