The Proterozoic P-T-t Evolution of the Kemp Land Coast, East Antarctica; Constraints from Si-saturated and Si-undersaturated Metapelites

Integrated metamorphic and geochronological data place new constraintson the metamorphic evolution of a Neoproterozoic orogen in eastAntarctica. Granulite-facies rocks from a 150 km stretch ofthe Kemp Land coast reflect peak conditions involving T 870–990°Cat P 7·4–10 kbar, with pressure increasing westwardtowards an Archaean craton. Electron microprobe-derived (Th+ U)–Pb monazite ages from metapelitic assemblages indicatethat the major mineral textures in these rocks developed duringthe c. 940 Ma Rayner Orogeny. Complex compositional zoning inmonazite suggests high-T recrystallization over c. 25 Myr. Diversityin metapelitic reaction textures reflects silica and ferromagnesiancontent: Si-saturated Fe-rich metapelites contain garnet thatis partially pseudomorphed by biotite and sillimanite, whereasSi-saturated Mg-rich metapelites and Si-undersaturated metapeliticpods have reaction microstructures involving cordierite enclosingorthopyroxene, garnet and/or sapphirine, cordierite + sapphirinesymplectites around sillimanite and coarse-grained orthopyroxene+ corundum separated by sapphirine coronae. Interpretationsbased on P–T pseudosections provide integrated bulk-rockconstraints and indicate a clockwise P–T–t pathcharacterized by a post-peak P–T trajectory with dP/dT 15–20 bar/ °C. This moderately sloped decompressive-coolingP–T path is in contrast to near-isothermal decompressionP–T paths commonly cited for this region of the RaynerComplex, with implications for the post-collisional tectonicresponse of the mid- to lower crust within this orogenic belt. KEY WORDS: electron microprobe monazite dating; granulite facies; Rayner Complex; sapphirine; THERMOCALCMinerals abbreviations: q, quartz; g, garnet; sill, sillimanite; ky, kyanite; opx, orthopyroxene; cd, cordierite; ksp, alkali feldspar; pl, plagioclase; bi, biotite; sp, spinel; ilm, ilmenite; mt, magnetite; ru, rutile; sa, sapphirine; cor, corundum; osm, osumilite; liq, silicate melt; mnz, monazite     

Metamorphism of Calcic Pelitic Schists, Strafford Dome, Vermont: Compositional Zoning and Reaction History

Four assemblages from calcic pelitic schists from South Strafford,Vermont, have been studied in detail to determine the relationshipbetween reaction history and compositional zoning of minerals.The lowest-grade assemblage is garnet + biotite + chlorite +plagioclase + epidote + quartz + muscovite + graphite + fluid.Along a path of isobaric heating, the net reaction is Chl +Ms + Ep + Gr = Grt + Bt + Pl + fluid. Garnet grows with decreasingFe/(Fe + Mg) and X_Spa, (from 0•2 to 0•05), X_Gra staysnearly constant between 0•20 and 0•25, and plagioclasegrows with X_An increasing from peristerite to 0•2–0•5. The subsequent evolution depends on whether chlorite or epidotereacts out first. If chlorite is removed from the assemblagefirst, the net reaction along an isobaric heating path becomesGrt + Ms + Ep + Qtz + Gr = Bt + Pl + fluid. X_An of plagioclaseincreases to 0•20–0•70, depending on the bulk-rockcomposition and changes in pressure and temperature. If epidoteis removed first, the assemblage becomes a simple pelite andthe net reaction becomes Chl + Pl + Ms + Qtz = Grt + Bt + H₂O.Plagioclase is consumed to provide Ca for growing garnet, andX_An, Fe/(Fe + Mg) of garnet, X_Gra, and X_Spa all decrease. Afterboth chlorite and epidote are removed, continued heating upto the metamorphic peak of {small tilde}600C produces littleprogress of the reaction Grt + Ms = Bt + Pl; and X_An increases. The four assemblages have been numerically modeled using theGibbs method starting with measured compositions. The modelssuccessfully predict the observed compositional zoning and trendsof mineral growth and consumption along the computed P–Tpaths. The models also predict the compositional mineral zoningthat would have resulted from other P–T paths. ^* Present address: Department of Geology, University of Alabama, Tuscaloosa, Alabama 35487     

Contrasting P-T Paths in the Eastern Himalaya, Nepal: Inverted Isograds in a Paired Metamorphic Mountain Belt

Petrology and phase equilibria of rocks from two profiles inEastern Nepal from the Lesser Himalayan Sequences, across theMain Central Thrust Zone and into the Greater Himalayan Sequencesreveal a Paired Metamorphic Mountain Belt (PMMB) composed oftwo thrust-bound metamorphic terranes of contrasting metamorphicstyle. At the higher structural level, the Greater HimalayanSequences experienced high-T/moderate-P metamorphism, with ananticlockwise P–T path. Low-P inclusion assemblages ofquartz + hercynitic spinel + sillimanite have been overgrownby peak metamorphic garnet + cordierite + sillimanite assemblagesthat equilibrated at 837 ± 59°C and 6·7 ±1·0 kbar. Matrix minerals are overprinted by numerousmetamorphic reaction textures that document isobaric coolingand re-equilibrated samples preserve evidence of cooling to600 ± 45°C at 5·7 ±1·1 kbar.Below the Main Central Thrust, the Lesser Himalayan Sequencesare a continuous (though inverted) Barrovian sequence of high-P/moderate-Tmetamorphic rocks. Metamorphic zones upwards from the loweststructural levels in the south are: Zone A: albite + chlorite + muscovite ± biotite; Zone B: albite + chlorite + muscovite + biotite + garnet; Zone C: albite + muscovite + biotite + garnet ± chlorite; Zone D: oligoclase + muscovite + biotite + garnet ± kyanite; Zone E: oligoclase + muscovite + biotite + garnet + staurolite+ kyanite; Zone F: bytownite + biotite + garnet + K-feldspar + kyanite± muscovite; Zone G: bytownite + biotite + garnet + K-feldspar + sillimanite+ melt ± kyanite. The Lesser Himalayan Sequences show evidence for a clockwiseP–T path. Peak-P conditions from mineral cores average10·0 ± 1·2 kbar and 557 ± 39°C,and peak-metamorphic conditions from rims average 8·8± 1·1 kbar and 609 ± 42°C in ZonesD–F. Matrix assemblages are overprinted by decompressionreaction textures, and in Zones F and G progress into the sillimanitefield. The two terranes were brought into juxtaposition duringformation of sillimanite–biotite ± gedrite foliationseams (S₃) formed at conditions of 674 ± 33°C and5·7 ± 1·1 kbar. The contrasting averagegeothermal gradients and P–T paths of these two metamorphicterranes suggest they make up a PMMB. The upper-plate positionof the Greater Himalayan Sequences produced an anticlockwiseP–T path, with the high average geothermal gradient beingpossibly due to high radiogenic element content in this terrane.In contrast, the lower-plate Lesser Himalayan Sequences weredeeply buried, metamorphosed in a clockwise P–T path anddisplay inverted isograds as a result of progressive ductileoverthrusting of the hot Greater Himalayan Sequences duringprograde metamorphism. KEY WORDS: thermobarometry; P–T paths; Himalaya; metamorphism; inverted isograds; paired metamorphic belts     

Petrology of Biotite-Cordierite-Garnet Gneiss of the McCullough Range, Nevada I. Evidence for Proterozoic Low-Pressure Fluid-Absent Granulite Grade Metamorphism in the Southern Cordillera

Proterozoic migmatitic paragneisses exposed in the McCulloughRange, southern Nevada, consist of cordierite+almanditic garnet+biotite+sillimanite+plagioclase+K-feldspar+quartz+ilmenite+hercynite.This assemblage is indicative of a low-pressure fades seriesat hornblende-granulite grade. Textures record a single metamorphicevent involving crystallization of cordierite at the expenseof biotite and sillimanite. Thermobarometry utilizing cation exchange between garnet, biotite,cordierite, hercynite, and plagioclase yields a preferred temperaturerange of 590–750?C and a pressure range of 3–4 kb.Equilibrium among biotite, sillimanite, quartz, garnet, andK-feldspar records a_H2O between 0?03 and 0?26. The low a_H2Otogetherwith low f_O2 (QFM) and optical properties of cordierite indicatemetamorphism under fluid-absent conditions. Preserved mineralcompositions are not consistent with equilibrium with a meltphase. Earlier limited partial melting was apparently extensiveenough to cause desiccation of the pelitic assemblage. The relatively low pressures attending high-grade metamorphismof the McCullough Range paragneisses allies this terrane withbiotite-cordierite-garnet granulites in other orogenic belts.aosure pressures and temperatures require a transient apparentthermal gradient ofat least 50?C/km during part of this Proterozoicevent in the southern Cordillera. ^*Present address: Institute of Geophysics and Planetary Physics, University of California, Los Angeles, CA 90024-1567     

Monazite-Xenotime Thermochronometry and Al2SiO5 Reaction Textures in the Picuris Range, Northern New Mexico, USA: New Evidence for a 1450-1400 Ma Orogenic Event

Al₂SiO₅ reaction textures in aluminous schist and quartziteof the northern Picuris range, north-central New Mexico, recorda paragenetic sequence of kyanite to sillimanite to andalusite,consistent with a clockwise P–T loop, with minor decompressionnear the Al₂SiO₅ triple-point. Peak metamorphic temperaturesare estimated at 510–525°C, at 4·0–4·2kbar. Kyanite and fibrolite are strongly deformed; some prismaticsillimanite, and all andalusite are relatively undeformed. Monaziteoccurs as inclusions within kyanite, mats of sillimanite andcentimetre-scale porphyroblasts of andalusite, and is typicallyaligned subparallel to the dominant regional foliation (S₀/S₁or S₂) and extension lineation (L₁). Back-scatter electron imagesand X-ray maps of monazite reveal distinct core, intermediateand rim compositional domains. Monazite–xenotime thermometryfrom the intermediate and rim domains yields temperatures of405–470°C (±50°C) and 500–520°C(±50°C), respectively, consistent with the progradeto peak metamorphic growth of monazite. In situ, ion microprobeanalyses from five monazites yield an upper intercept age of1417 ± 9 Ma. Near-concordant to concordant analyses yield²⁰⁷Pb–²⁰⁶Pb ages from 1434 ± 12 Ma (core) to 1390± 20 Ma (rim). We find no evidence of older regionalmetamorphism related to the 1650 Ma Mazatzal Orogeny. KEY WORDS: Al₂SiO₅; metamorphism; monazite; thermochronometry; triple-point     

Reaction Textures in a Suite of Spinel Granulites from the Eastern Ghats Belt, India: Evidence for Polymetamorphism, a Partial Petrogenetic Grid in the System KFMASH and the Roles of ZnO and Fe2O3

Spinel granulites, with or without sapphirine, occur as lensesin garnetiferous quartzofeldspathic gneisses (leptynites) nearGokavaram in the Eastern Ghats Belt, India. Spinel granulitesare mineralogically heterogeneous and six mineral associationsoccur in closely spaced domains. These are (I) spinel–quartz–cordierite,(II) spinel–quartz–cordierite–garnet–orthopyroxene–sillimanite,(III) spinel–cordierite–orthopyroxene–sillimanite,(IV) spinel–quartz–sapphirine–sillimanite–garnet,(V) spinel–quartz-sapphirine–garnet and (IV) rhombohedral(Fe–Ti) oxide–cordierite–orthopyroxene–sillimanite.Common to all the associations are a porphyroblastic garnet(containing an internal schistosify defined by biotite, sillimaniteand quartz), perthite and plagioclase. Spinel contains variableamounts of exsolved magnetite and is distinctly Zn rich in thesapphirine-absent associations. X_Mg in the coexisting phasesdecreases in the order cordierite–biotite–sapphirine–orthopyroxene–spinel–garnet–(Fe–Ti)oxides. Textural criteria and compositional characteristicsof the phases document several retrograde mineral reactionswhich occurred subsequent to prograde dehydration melting reactionsinvolving biotite, sillimanite, quartz, plagioclase and spinel.The following retrograde mineral reactions are deduced: (1)spinel + quartz cordierite, (2) spinel + quartz garnet + sillimanite,(3) garnet + quartz cordierite + orthopyroxene, (4) garnet+ quartz + sillimanite cordierite, (5) spinel + cordierite orthopyroxene + sillimanite, (6) spinel + sillimanite + quartz sapphirine, (7) spinel + sapphirine + quartz garnet + sillimanite,and (8) spinel + quartz sapphirine + garnet. A partial petrogeneticgrid for the system FeO–MgO–Al₂O₃–SiO₂–K₂O–H₂Oat high fo₂, has been constructed and the effects of ZnO andFe₂O₃ on this grid have been explored Combining available experimentaland natural occurrence data, the high fo₂ invariant points inthe partial grid have been located in P–T space. Geothermobarometricdata and consideration of the deduced mineral reactions in thepetrogenetic grid show that the spinel granulites evolved throughan anticlockwise P–T trajectory reaching peak metamorphicconditions >9 kbar and 950C, followed by near-isobaric cooling(dT/dP = 150C/kbar). This was superimposed by an event of near-isothermaldecompression (dT/dP = 15C/kbar). The studied spinel granulites,therefore, preserve relic prograde mineral associations andreaction textures despite being metamorphosed at very high temperatures,and bear evidence of polymetamorphism. KEY WORDS: spinel granulite; Eastern Ghats; India; polymetamorphism; geothermometry; geobarometry Corresponding author     

Orthopyroxene-Corundum in Mg-Al-rich Granulites from the Oygarden Islands, East Antarctica

High-Mg–Al, silica-undersaturated metapelites from theOygarden Group of islands, East Antarctica, preserve clear evidencefor the stable coexistence of the assemblage orthopyroxene +corundum in natural rocks. The quartz-absent metapelite occursas pods and isolated layers within a high-strain zone relatedto deformation during the c. 0·93 Ga Rayner StructuralEpisode. Assemblages that include orthopyroxene, corundum, sapphirine,sillimanite, cordierite, garnet and kornerupine are developedacross a pre-existing compositional zoning, leading to contrastingmineral Fe–Mg ratios. The assemblage orthopyroxene–corundumis shown to exist in only a very restricted range of bulk compositionsand P–T histories. Simplified qualitative FMAS grids havebeen constructed for kornerupine-absent and -present systems,illustrating MAS terminations and divariant equilibria thathelp to describe the mineral assemblage and reaction history.Reaction textures that include coronas of sapphirine and sillimaniteseparating orthopyroxene and corundum, and symplectites of orthopyroxene+ sapphirine ± cordierite/plagioclase, orthopyroxene+ sillimanite ± cordierite/plagioclase and orthopyroxene+ sapphirine + sillimanite embaying garnet, imply a clockwiseP–T–t evolution. Conditions of P > 9–10kbar and T     

Mg-Al Sapphirine- and Ca-Al Hibonite-bearing Granulite Xenoliths from the Chyulu Hills Volcanic Field, Kenya

Basanites of the Chyulu Hills (Kenya Rift) contain mafic Mg–Aland Ca–Al granulite xenoliths. Their protoliths are interpretedas troctolitic cumulates; however, the original mineral assemblageswere almost completely transformed by subsolidus reactions.Mg–Al granulites contain the minerals spinel, sapphirine,sillimanite, plagioclase, corundum, clinopyroxene, orthopyroxeneand garnet, whereas Ca–Al granulites are characterizedby hibonite, spinel, sapphirine, mullite, sillimanite, plagioclase,quartz, clinopyroxene, corundum, and garnet. In the Mg–Algranulites, the first generation of orthopyroxene and some spinelmay be of igneous origin. In the Ca–Al granulites, hibonite(and possibly some spinel) are the earliest, possibly igneous,minerals in the crystallization sequence. Most pyroxene, spineland corundum in Mg–Al and Ca–Al granulites formedby subsolidus reactions. The qualitative P–T path derivedfrom metamorphic reactions corresponds to subsolidus cooling,probably accompanied, or followed by, compression. Final equilibrationwas achieved at T 600–740°C and P <8 kbar, inthe stability field of sillimanite. The early coexistence ofcorundum and pyroxenes (± spinel), as well as the associationof sillimanite and sapphirine with clinopyroxene and the presenceof hibonite, makes both types of granulite rare. The Ca–Alhibonite-bearing granulites are unique. Both types enlarge thespectrum of known Ca–Al–Mg-rich granulites worldwide. KEY WORDS: granulite xenoliths; corundum; sapphirine; hibonite; Kenya Rift     

Metamorphic P-T Paths from Cordillera Darwin, a Core Complex in Tierra del Fuego, Chile

P–T conditions and prograde P–T paths have beencalculated for amphibolite-grade pelites and amphibolites fromCordillera Darwin, Tierra del Fuego, Chile. Peak P–T conditionsare nearly all within the kyanite stability field; temperaturesgenerally show an increase with increasing grade, but pressureshave a less consistent trend, possibly increasing slightly fromgarnet to kyanite grade. P–T paths from pelites show heatingby 80–100C during loading of 0•2–3 kbar. Texturalanalysis and previous structural work indicate that this segmentof the path correlates with back-folding deformation. P–Tpaths from two Mg-rich garnet amphibolites suggest a decreasein pressure of as much as 3 kbar with 25–50C of heatingfrom the kyanite stability field to the sillimanite, and areconsistent with pervasive, minor development of fibrolitic sillimanitealong plagioclase grain boundaries. Together, the P–Tpath segments from pelites and amphibolites constitute a clockwiseP–T trajectory. The proposed clockwise P–T paths are consistent with theinterpretation that Cordillera Darwin represents an extensionallyexhumed metamorphic core complex, in which loading during garnetgrowth in the pelitic rocks was succeeded by differential upliftduring garnet growth in magnesian amphibolites. ^* Present address: Department of Geology and Geophysics, University of Wisconsin, Madison, Wisconsin 53706     

A Biotite Isograd in South-Central Maine, U.S.A.: Mineral Reactions, Fluid Transfer, and Heat Transfer

The biotite isograd in pelitic schists of the Waterville Formationinvolved reaction of muscovite + ankerite + rutile + pyrite+graphite + siderite or calcite to form biotite + plagioclase+ ilmenite. There was no single reaction in all pelites; eachrock experienced a unique reaction depending on the mineralogyand proportions of minerals in the chlorite-zone equivalentfrom which it evolved. Quartz, chlorite, and pyrrhotite werereactants in some rocks and products in others. All inferredbiotite-forming reactions involved decarbonation and desulfidation;some were dehydration reactions and others were hydration reactions.P-T conditions at the biotite isograd were near 3500 bars and400 °C. C-O-H-S fluids in equilibrium with the pelitic rockswere close to binary CO₂-H₂O mixtures with X_CO2 = 0.02–0.04.During the biotite-forming reaction, pelitic rocks (a) decreasedby 2–5 percent in volume, (b) performed – (4–11)kcal/liter P-V work on their surroundings, (c) absorbed 38–85kcal/liter heat from their surroundings, and (d) were infiltratedby at least 0.9–2.2 rock volumes H₂O fluid. The biotite isograd sharply marks the limit of a decarbonationfront that passed through the terrane during regional metamorphism.Decarbonation converted meta-shales with 6–10 per centcarbonate to carbonate-free pelitic schists. One essential causeof the decarbonation event was pervasive infiltration of theterrane by at least 1–2 rock volumes H₂O fluid early inthe metamorphic event under P-T conditions of the biotite isograd.Average shale contains 4–13 per cent siderite, ankerite,and/or calcite, but average pelitic schist is devoid of carbonateminerals. If the Waterville Formation serves as a general modelfor the metamorphism of pelitic rocks, it is likely that worldwidemany pelitic schists developed by decarbonation of shale caused,in part, by pervasive infiltration of metamorphic terranes byseveral rock volumes of aqueous fluid during an early stageof the metamorphic event.     

Mineral Chemistry and Metasomatic Growth of Aluminous Enclaves in Gedrite--Cordierite-Gneiss from Southwestern New Hampshire, USA

The aluminous enclaves occur in gedrite-cordierite-gneissesof the Middle Ordovician Ammonoosuc Volcanics, and are composedof combinations of the aluminous minerals sillimanite (Sill),kyanite, corundum (Cor), staurolite (St), sapphirine (Sa), andspinel (Sp), which are set in a matrix of cordierite (Crd) orplagioclase (Plag). Generally, where plagioclase is present,both it and the aluminous minerals are separated from gedrite(Ged) and rare hornblende (Hbl) by cordierite. The enclavesarc interpreted to have formed near the peak of Acadian (Devonian)metamorphism at sillimanite-staurolite-muscovite grade by reactionsthat were encountered during the pressure decrease which accompaniedthe rise of gneiss domes in the region. The enclaves are divided into two main types: (1) enclaves ofcordierite surrounding aluminous minerals; and (2) enclavesof cordierite and plagioclase surrounding aluminuous minerals.Sapphirine grains contain between 9?2 and 9?3 Al atoms per formulacalculated to 14 cations. Staurolites from the enclaves areMg-rich and have (Fe²⁺+ Mn)/(Fe²⁺+Mn+Mg) ratios of 0-59–0?64. The textures and mineralogy of the enclaves suggest that theserocks originally consisted of Ged+Sill?Qz?Hbl?Sp?Plag. Theseminerals reacted to form Crd+Aluminous Minerals?Plag. The mineralogyof both main types of enclaves can be explained by two analogoussets of continuous Fe-Mg reactions:The structure of the enclavessuggests that the mineral growth by the above reactions wasdiffusion controlled, which would have resulted from oversteppingthe above reactions (i.e. the P change exceeded the reactionrate). Therefore, chemical potential gradients (relative mobilityof diffusing components) between gedrite and sillimanite controlledthe location of mineral growth. The Fe-Mg ratio of the bulkcomposition and the proportions of non-Fe-Mg minerals (quartzand sillimanite) appear to determine which continuous Fe-Mgreactions were encountered. Examples of mineral sequences in the cordierite enclaves are:Sill (core)/St+Crd/Ged (matrix); Cor+Crd (core)/Ged (matrix),and Sill (core)/St+Crd/Sa+Crd/Ged (matrix). Examples of themineral sequences in the cordierite-plagioclase enclaves are:Sill (core)/St+Plag/Plag+Crd/Hbl+Ged (matrix); Cor+Plag (core)/St+Plag/Sa+Plag/Ged+ Hbl (matrix); and St+Plag (core)/Plag+Crd/Ged+Hbl (matrix). P–µ_FeMg–1 diagrams proved to be an importanttool for understanding and illustrating the development of theenclaves. These diagrams allow one to view simultaneously allthe discontinuous and continuous Fe-Mg reactions along a P–µ_H2O(or T) rock path. With this information it is possible to determinequalitatively which reactions and what sequence of reactionsmight be encountered by bulk compositions with variable Fe-Mgratios and modal proportions of phases.     

Fluid Flow During Contact Metamorphism of Ophicarbonate Rocks in the Bergell Aureole, Val Malenco, Italian Alps

Contact-mctamorphic assemblages in ophicarbonate from the Bergellaureole correspond either to model isobaric invariant T-XCO₂points [Atg-Cal-Di-Tr-Fo (6 samples) and Atg-Cal-Tr-Fo-Dol (2)]or to isobaric univariant T-XCO₂, curves [Tr-Cal-Di-Atg (18),Tr-Dol-Atg-Cal (1), Atg-Cal-Fo-Di (1), and Atg-Cal-Tr-Fo (1)].Calcite-dolomite thermometry and mineral-fluid equilibria inthe invariant assemblages record T=440–540C at P=3•5kbar. Equilibrium metamorphic fluids were very H₂O rich withX CO₂,=0•001–0•027. In the invariant assemblagesTr + Fo were produced by prograde decarbonation-dehydrationreactions. In contrast, measured modes and reaction texturesin samples with univariant assemblages indicate thai Tr wasproduced by carbonation reactions. The apparent paradox of simultaneousdecarbonation reactions in the model isobaric invariant assemblagesand carbonation reactions in univariant assemblages is resolvedby local mineral-fluid equilibrium and fluid flow through ophicarbohatesin the direction of decreasing temperature as the aureole heated.Time-integrated flux (q) was computed from measured reactionprogress in 28 samples for models of both horizontal and verticaldown-temperature flow. Results are similar, with q decreasingrapidly from (0•2–5•1) 10⁵ cm³ fluid/cm² rock1•3–1•7 km from the intrusion to 0–0•610⁵cm³/cm² at 1•8–4•0 km. The decrease in q ismore consistent with vertical than horizontal flow. Variationsin time-integrated flux of more than an order of magnitude arerecorded by samples from the same outcrop. The absence of carbonatein adjacent metaperidotite indicates that flow was confinedto the ophicarbonate. Channelized, spatially heterogeneous,vertical flow can be explained by the brecciation and strongvertical foliation of the ophicarbonate relative to surroundingmassive metaperidotite. Generation of metamorphicfluids by decarbonation-dehydrationreactions within the ophicarbonates explains larger averageflux 1–2 km from the intrusion compared with more distalpoints. KEY WORDS: Bergell; contact metamorphism; fluid flow; ophicarbonate ^*Telephone: (410) 516-8121. Fax: (410) 516-7933     

The Prinsen af Wales Bjerge Formation Lavas, East Greenland: the Transition from Tholeiitic to Alkalic Magmatism during Palaeogene Continental Break-up

We present elemental and isotopic (Sr–Nd–Pb–Hf–Os–He)data on primitive alkalic lavas from the Prinsen af Wales Bjerge,East Greenland. Stratigraphical, compositional and ⁴⁰Ar–³⁹Ardata indicate that this inland alkalic activity was contemporaneouswith the upper parts of the main tholeiitic plateau basaltsand also post-dated them. The alkalic rocks show a marked crustalinfluence, indicating establishment of new magmatic plumbingsystems distinct from the long-lived coastal systems that fedthe relatively uncontaminated plateau basalts. The least contaminatedlavas have high ³He/⁴He isotope ratios (R/R_A 12·4–18·5),sub-chondritic ¹⁸⁷Os/¹⁸⁸Os_i (0·120–0·126),low     

Melting and Thermal Reconstitution of Pelitic Xenoliths, Wehr Volcano, East Eifel, West Germany

Pelitic xenoliths derived from amphibolite grade basement rocksoccur within a Pleistocene, trachytic, pyroclastic unit of theWehr volcano, East Eifel, West Germany: With increasing temperatureand/or prolonged heating at high temperature, quartz-plagioclaseand micaceous layers of the xenoliths have undergone meltingto form buchites and thermal reconstitution by dehydration reactions,melting and crystallization to form restites respectively. Thexenoliths provide detailed evidence of melting, high temperaturedecomposition of minerals, nucleation and growth of new phasesand P-T-f_o2 conditions of contact metamorphism of basement rocksby the Wehr magma. Melting begins at quartz-oligoclase (An_17·3Ab_82·3Or_0·4-An_20·0Ab_78·1Or_1·9)grain boundaries in quartz-plagioclase rich layers and the amountof melting is controlled by H₂O and alkalis released duringdehydroxylation/oxidation of associated micas. Initially, glasscompositions are heterogeneous, but with increasing degreesof melting they become more homogeneous and are similar to S-typegranitic minimum melts with SiO₂ between 71 and 77 wt. per cent;A/(CNK) ratios of 1·2–1·4; Na₂O < 2·95and normative corundum contents of 1·9–4·0per cent. Near micas plagioclase melts by preferential dissolutionof the NaAlSi₃O₈ component accompanied by a simultaneous increasein CaAl²Si²O⁸ (up to 20 mol. per cent An higher than the bulkplagioclase composition) at the melting edge. With increasingtemperature the end product of fractional melting is the formationand persistence of refractory bytownite (An_78–80) in thosexenoliths where extensive melting has taken place. Initial stage decomposition of muscovite involves dehydroxylation(H₂O and alkali loss). At higher temperatures muscovite breaksdown to mullite, sillimanite, corundum, sanidine and a peraluminousmelt. Mullite (40–43 mol. per cent SiO₂) and sillimanite(49 mol. per cent SiO₂) are Fe₂O₃ and TiO₂ rich (up to 6·1–0·84and 3·6–0·24 wt. per cent respectively).Al-rich mullite (up to 77 wt. per cent Al₂O₃) occurs with corundumwhich has high Fe₂O₃ and TiO₂ (up to 6·9 and 2·1wt. per cent respectively). Annealing at high temperatures andreducing conditions results in the exsolution of mullite fromsillimanite and ilmenite from corundum. Glass resulting fromthe melting of muscovite in the presence of quartz is peraluminous(A/(CNK) = 1·3) with SiO² contents of 66–69 percent and normative corundum of 4 per cent. Sanidine (An_1·9Ab_26·0Or_72·1-An_1·3Ab_15·9Or_82·9)crystallized from the melt. Dehydroxylation and oxidation of biotite results in a decreaseof K₂O from 8·6 to less than 1 wt. per cent and oxidetotals (less H₂O + contents) from 96·5 to 88·6,exsolution of Al-magnetite, and a decrease in the Fe/(Fe + Mg)ratio from 0·41 to 0·17. Partial melting of biotitein the presence of quartz/plagioclase to pleonaste, Al-Ti magnetite,sanidine(An_2·0Ab_34·9Or63·1) and melt takesplace at higher temperatures. Glass in the vicinity of meltedbiotite is pale brown and highly peraluminous (A/CNK = 2·1)with up to 6 wt. per cent MgO+FeO_{(total iroq)} and up to 10 percent normative corundum. Near liquidus biotite with higher Al₂O₃and TiO₂ than partially melted biotite crystallized from themelt. Ti-rich biotites (up to 6 wt. per cent TiO₂) occur withinthe restite layers of thermally reconstituted xenoliths. Meltingof Ti-rich biotite and sillimanite in contact with the siliceousmelt of the buchite parts of xenoliths resulted in the formationof cordierite (100 Mg/(Mg+Fe+Mn) = 76·5–69·4),Al-Ti magnetite and sanidine, and development of cordierite/quartzintergrowths into the buchite melt. Growth of sanidine enclosedrelic Ca-plagioclase to form patchy intergrowths in the restitelayers. Cordierite (100 Mg/(Mg+Fe+Mn) = 64–69), quartz,sillimanite, mullite, magnetite and ilmenite, crystallized fromthe peraluminous buchite melt. Green-brown spinels of the pleonaste-magnetite series have awide compositional variation of (mol. per cent) FeAl₂O₄—66·6–45·0;MgAl₂O₄—53·0–18·7; Fe₃O₄—6·9–28·1;MnAl₂O₄—1·2–1·5; Fe₂TiO₄—0·6–6·2.Rims are generally enriched in the Fe₃O₄ component as a resultof oxidation. Compositions of ilmenite and magnetite (single,homogeneous and composite grains) are highly variable and resultfrom varying degrees of high temperature oxidation that is associatedwith dehydroxylation of micas and melting. Oxidation mainlyresults in increasing Fe³⁺, Al and decreasing Ti⁴⁺, Fe²⁺ inilmenite, and increasing Fe²⁺, Ti⁴⁺ and decreasing Fe³⁺ in associatedmagnetite. A higher degree of oxidation is reached with exsolutionof rutile from ilmenite and formation of titanhematite and withexsolution of pleonaste from magnetite. Ti-Al rich magnetite(5·1–7·5 and 8·5–13·5wt. per cent respectively) and ilmenite crystallized from meltsin buchitic parts of the xenoliths. Chemical and mineralogic evidence indicates that even with extensivemelting the primary compositions of individual layers in thexenoliths remained unmodified. Apparently the xenoliths didnot remain long enough at high temperatures for desilicationand enrichment in Al₂O₃, TiO₂, FeO, Fe₂O₃, and MgO that resultsby removal of a ‘granitic’ melt, and/or by interactionwith the magma, to occur. T °C-f_o2 values calculated from unoxidized magnetite/ilmenitegive temperatures ranging from 615–710°C for contactmetamorphism and the beginning of melting, and between 873 and1054°C for the crystallization of oxides and mullite/sillimanitefrom high temperature peraluminous melts. f_o2 values of metamorphismand melting were between the Ni-NiO and Fe₂O₃-Fe₃O₄ buffer curves.The relative abundance of xenolith types, geophysical evidenceand contact metamorphic mineralogy indicates that the xenolithswere derived from depths corresponding to between 2–3kb P_load = P_fluid. The xenoliths were erupted during the latestphreatomagmatic eruption from the Wehr volcano which resultedin vesiculation of melts in partially molten xenoliths causingfragmentation and disorientation of solid restite layers.     

Zoned Poikiloblastic Garnets: P-T Paths and Syn-Metamorphic Uplift through 30 km of Structural Depth, Wopmay Orogen, Canada

In the early Proterozoic Wopmay Orogen (Northwest Territories,Canada), the occurrence of garnet-biotite-sillimanite/kyanite-plagioclase-quartzassemblages in pelitic schists at a variety of obliquely exposedstructural levels enables the use of calibrated geothermometersand geobarometers through 30 km of composite structural relief.Direct derivation of multipoint P-T paths from single garnetsis attained from core-to-rim microprobe analyses of zoned poikiloblasticgarnets, which contain biotite, plagioclase, quartz, and lesscommonly Al₂SiO₅ inclusions. The documented garnet zoning andthe entrapment of the mineral inclusions is compatible withpartial-equilibrium growth models. The lack of significant diffusionre-equilibration in the garnet interiors is favored by samplerestriction to medium-grade schists and is attested by the preservationof normal-zoning profiles, the lack of garnet diffusion babesaround biotite inclusions, the matching composition trends ofgarnet-core to -rim plagioclase inclusions with those of zonedmatrix plagioclase grains, and the systematic variation of thederived P-T data. Only the garnet rims, which are characterizedby a reversal of compositional trends and by textural resorption,are interpreted to indicate local post-thermal-peak re-equilibration. The calculated P-T paths quantify segments of uplift trajectoriescorresponding to pressure drops of 2?5–1?5 kb from maximaof 9?3–5?0 kb depending on structural level. This is concurrentwith initial increases of 25–75?C to peak-temperatureconditions and is followed by variable drops in temperatureduring continued decompression. Individual paths are consistentwith modelled variations of metamorphic conditions as a functionof loading, uplift, and erosion in overthrust terrains. Consideredwith U-Pb zircon geochronological data the P-T paths, studiedas a set, indicate an average uplift rate that varies spatiallyfrom 1?5–2?7 mm y^–1. This variation can be relatedto late cross folding of the orogenic internal zone, suggestingthat the syn-metamorphic uplift was structurally controlled.The distribution of peak-temperature conditions attained duringdecompression is independent of structural depth. This, andthe inverted metamorphism documented in the Wopmay Orogen, requirethat final variations in temperature result from thermal relaxationof isotherms in, and away from, a hot crustal allochthon composedin part of high-T rift-fill units and a syntectonic graniticbatholith.     

Petrogenesis of Early Neogene Magmatism in the Northern Puna; Implications for Magma Genesis and Crustal Processes in the Central Andean Plateau

New compositional data and petrogenetic models are presentedfor pre-Upper Miocene volcanism in the northern Puna of Argentina(22°S–24°S). Two phases of volcanism producedsmall dome complexes of mainly silicic andesite to low-SiO₂rhyolite. The Upper Oligocene–Lower Miocene phase (UOLM,20–17 Ma), produced two distinct groups of rocks. TheUOLM-1 group is metaluminous and mainly andesitic, with isotopiccompositions like those of the recent arc (⁸⁷Sr/⁸⁶Sr_T     

Ultrahigh-temperature Metamorphism (1150{degrees}C, 12 kbar) and Multistage Evolution of Mg-, Al-rich Granulites from the Central Highland Complex, Sri Lanka

Mg- and Al-rich granulites of the central Highland Complex,Sri Lanka preserve a range of reaction textures indicative ofa multistage P–T history following an ultrahigh-temperaturemetamorphic peak. The granulites contain a near-peak assemblageof sapphirine–garnet–orthopyroxene–sillimanite–quartz–K-feldspar,which was later overprinted by intergrowth, symplectite andcorona textures involving orthopyroxene, sapphirine, cordieriteand spinel. Biotite-rims, kornerupine and orthopyroxene-rimson biotite are considered to be late assemblages. Thermobarometriccalculations yield an estimated P–T of at least 1100°Cand 12 kbar for the near-peak metamorphism. Isopleths of Al₂O₃in orthopyroxene are consistent with a peak temperature above1150°C. The P–T path consists of four segments. Initialisobaric cooling after peak metamorphism (Segment A), whichproduced the garnet–sapphirine–quartz assemblage,was followed by near-isothermal decompression at ultrahigh temperature(Segment B), which produced the multiphase symplectites. Furtherisobaric cooling (Segment C) resulted in the formation of biotiteand kornerupine, and late isothermal decompression (SegmentD) formed orthopyroxene rims on biotite. This evolution canbe correlated with similar P–T paths elsewhere, but thereare not yet sufficient geochronological and structural dataavailable from the Highland Complex to allow the tectonic implicationsto be fully assessed. KEY WORDS: central Highland Complex; granulites; multistage evolution; Sri Lanka; UHT metamorphism     

Petro-tectonic Imprints in the Sapphirine Granulites from Anantagiri, Eastern Ghats Mobile Belt, India

Sapphirine granulite occurring as lenses in charnockite at Anantagiri,Eastern Ghat, India, displays an array of minerals which developedunder different P-T-X conditions. Reaction textures in conjunctionwith mineral chemical data attest to several Fe-Mg continuousreactions, such as

1. spinel+rutile+quartz+MgFe_–1=sapphirine+ilmenite
2. cordierite=sapphirine+quartz+MgFe_–1
3. sapphirine+quartz=orthopyroxene+sillimanite+MgFe_–1
4. orthopyroxene+sapphirine+quartz=garnet+MgFe_–1
5. orthopyroxene+sillimanite=garnet+quartz+MgFe_–1
6. orthopyroxene+sillimanite+quartz+MgFe_–1=cordierite.

Calculated positions of the reaction curves in P-T space, togetherwith discrete P-T points obtained through geothermobarometryin sapphirine granulite and the closely associated charnockiteand mafic granulite, define an anticlockwise P-T trajectory.This comprises a high-T/P prograde metamorphic path which culminatedin a pressure regime of 8?3 kb above 950?C, a nearly isobariccooling (IBC) path (from 950?C, 8?3 kb, to 675?C, 7?5kb) anda terminal decompressive path (from 7?5 to 4?5 kb). Spinel,quartz, high-Mg cordierite, and sapphirine were stabilized duringthe prograde high-T/P metamorphism, followed by the developmentof orthopyroxene, sillimanite, and garnet during the IBC. Retrogradelow-Mg cordierite appeared as a consequence of decompressionin the sapphirine granulite. Deformational structures, reportedfrom the Eastern Ghat granulites, and the available geochronologicaldata indicate that prograde metamorphism could have occurredat 30001?00 and 2500?100 Ma during a compressive orogeny thatwas associated with high heat influx through mafic magmatism. IBC ensued from P_max and was thus a direct consequence of progrademetamorphism. However, in the absence of sufficient study onthe spatial variation in P-T paths and the strain historiesin relation to time, the linkage between IBC and isothermaldecompression (ITD) has remained obscure. A prolonged IBC followedby ITD could be the consequence of one extensional mechanismwhich had an insufficient acceleration at the early stage, orITD separately could be caused by an unrelated extensional tectonism.The complex cooled nearly isobarically from 2500 Ma. It sufferedrapid decompression accompanied by anorthosite and alkalinemagmatism at 1400–1000 Ma.     

Formation of Wollastonite by Chemically Reactive Fluid Flow During Contact Metamorphism, Mt. Morrison Pendant, Sierra Nevada, California, USA

Quartz–calcite sandstones experienced the reaction calcite+ quartz = wollastonite + CO₂ during prograde contact metamorphismat P = 1500 bars and T = 560°C. Rocks were in equilibriumduring reaction with a CO₂–H₂O fluid with XCO₂ = 0·14.The transition from calcite-bearing, wollastonite-free to wollastonite-bearing,calcite-free rocks across the wollastonite isograd is only severalmillimeters wide. The wollastonite-forming reaction was drivenby infiltration of quartz–calcite sandstone by chemicallyreactive H₂O-rich fluids, and the distribution of wollastonitedirectly images the flow paths of reactive fluids during metamorphism.The mapped distribution of wollastonite and modeling of an O-isotopeprofile across a lithologic contact indicate that the principaldirection of flow was layer-parallel, directed upward, withany cross-layer component of flow <0·1% of the layer-parallelcomponent. Fluid flow was channeled at a scale of 1–100m by pre-metamorphic dikes, thrust and strike-slip faults, foldhinges, bedding, and stratigraphic contacts. Limits on the amountof fluid, based on minimum and maximum estimates for the displacementof the wollastonite reaction front from the fluid source, are(0·7–1·9) x 10⁵ cm³ fluid/cm² rock. Thesharpness of the wollastonite isograd, the consistency of mineralthermobarometry, the uniform measured ¹⁸O–¹⁶O fractionationsbetween quartz and calcite, and model calculations all arguefor a close approach to local mineral–fluid equilibriumduring the wollastonite-forming reaction. KEY WORDS: contact metamorphism, fluid flow, wollastonite, oxygen isotopes, reaction front     

The Relationship between Tectono-metamorphic Evolution and Argon Isotope Records in White Mica: Constraints from in situ 40Ar-39Ar Laser Analysis of the Variscan Basement of Sardinia

The basement of Sardinia represents a nearly complete sectionof a segment of the Variscan belt that experienced a polyphasetectono-metamorphic evolution and Barrovian metamorphism. Thisbasement is well suited to investigate the relationship betweentectono-metamorphic evolution and argon isotope records in whitemica. Micaschists from the garnet zone (maximum T of up to 520–560°C)contain two texturally and chemically resolvable generationsof white mica: (1) deformed celadonite-rich flakes, defininga relict S₁ foliation preserved within the main S₂ foliationor enclosed in rotated albite porphyroblasts; (2) celadonite-poorwhite micas aligned along the main S₂ foliation. The S₁ foliationdeveloped earlier and at a deeper crustal level with respectto that at which the thermal peak was reached. From the staurolitezone (T of up to 590–625°C) to the sillimanite + K-feldsparzone, white mica is nearly uniform in composition (muscovite)and is predominantly aligned along the S₂ foliation or is oflater crystallization. In situ ⁴⁰Ar–³⁹Ar laser analysesof white mica yielded ages of