Petrology and geothermobarometry of granulite facies metapelites from the Hisøy-Torungen area, south Norway: new data on the Sveconorvegian P–T–t path of the Bamble sector

ABSTRACT The high-grade rocks (metapelite, quartzite, metagabbro) of the Hisøy-Torungen area represent the south-westernmost exposures of granulites in the Proterozoic Bamble sector, south Norway. The area is isoclinally folded and a metamorphic P–T–t path through four successive stages (M1-M4) is recognized. Petrological evidence for a prograde metamorphic event (M1) is obtained from relict staurolite + chlorite + albite, staurolite + hercynite + ilmenite, cordierite + sillimanite, fine-grained felsic material + quartz and hercynite + biotite ± sillimanite within metapelitic garnet. The phase relations are consistent with a pressure of 3.6 ± 0.5 kbar and temperatures up to 750–850°C. M1 is connected to the thermal effect of the gabbroic intrusions prior to the main (M2) Sveconorwegian granulite facies metamorphism. The main M2 granulite facies mineral assemblages (quartz+ plagioclase + K-feldspar + garnet + biotite ± sillimanite) are best preserved in the several-metre-wide Al-rich metapelites, which represent conditions of 5.9–9.1 kbar and 790–884°C. These P–T conditions are consistent with a temperature increase of 80–100°C relative to the adjacent amphibolite facies terranes. No accompanying pressure variations are recorded. Up to 1-mm-wide fine-grained felsic veinlets appear in several units and represent remnants of a former melt formed by the reaction: Bt + Sil + Qtz→Grt + lq. This dehydration reaction, together with the absence of large-scale migmatites in the area, suggests a very reduced water activity in the rocks and XH₂O = 0.25 in the C–O–H fluid system was calculated for a metapelitic unit. A low but variable water activity can best explain the presence or absence of fine-grained felsic material representing a former melt in the different granulitic metapelites. The strongly peraluminous composition of the felsic veinlets is due to the reaction: Grt +former melt ± Sil→Crd + Bt ± Qtz + H₂O, which has given poorly crystalline cordierite aggregates intergrown with well-crystalline biotite. The cordierite- and biotite-producing reaction constrains a steep first-stage retrograde (relative to M2) uplift path. Decimetre- to metre-wide, strongly banded metapelites (quartz + plagioclase + biotite + garnet ± sillimanite) inter-layered with quartzites are retrograded to (M3) amphibolite facies assemblages. A P–T estimate of 1.7–5.6 kbar, 516–581°C is obtained from geothermobarometry based on rim-rim analyses of garnet–biotite–plagioclase–sillimanite–quartz assemblages, and can be related to the isoclinal folding of the rocks. M4 greenschist facies conditions are most extensively developed in millimetre-wide chlorite-rich, calcite-bearing veins cutting the foliation.     

Petrological and Geochemical Evidence for Granitoid Formation: The Waldoboro Pluton Complex, Maine

The Acadian-age Waldoboro Pluton Complex (WPC), mid-coastalMaine, consists of seven granitoid units surrounded by migmatitic,peraluminous gneisses and schists (predominantly Bucksport orSebascodegan Formation). The complex (area >340 km²) cross-cutsthe westward-vergent St. George thrust fault, which may markthe boundary between the Avalon and Gander composite terranes.Field and petrologic data indicate in situ formation of theperaluminous, syntectonic granitoids: contacts with Bucksportparagneisses are transitional and concordant; abundant country-rockenclaves show evidence for melting; restitic garnet, biotite,and plagioclase in the granitoids are identical in compositionto garnet, biotite, and plagioclase in the country rock. Chemicalvariations among the main granitoid phases (gneissic granite,granite, and leucogranite) reflect varying degrees of melt-restiteunmixing. Major and trace elements define mixing trends betweenrefractory Bucksport lithologies and leucogranites which approximatemelt compositions. Petrographic and whole-rock chemical dataare consistent with restitic plagioclase, garnet, biotite, tourmaline,zircon, apatite, sphene, and an accessory phase such as monazite.Quantitative major-oxide mass-balance models indicate that gneissicgranite represents a mixture of 55% melt–45% restite whereasgranite represents a mixture of 76% melt–24% restite.Melt-restite proportions calculated from trace element dataagree with those calculated from major oxide data for the gneissicgranite, but are different (85% melt–15% restite) fromthose calculated from major oxide data for the granite. Thisis attributed to inhomogeneous distribution of minor phasesand the effects of metasomatism. High K₂O, Rb, Ba, Cs, Li, B,K/Rb, K/Ba, Rb/Sr, and Th/U along the eastern mylonitic marginand elsewhere within the WPC reflect post-solidification metasomaticprocesses. Intrusion of mafic magmas during uplift after crustal thickeningappears to have caused high-temperature metamorphism and anatexisof Bucksport country rocks at relatively low pressure (0.4 GPa).Dehydration melting of muscovite to produce magmas saturatedor nearly saturated with H₂O explains the formation of migmatitesin the vicinity of the WPC. Formation of granites by 50–60%fluid-absent melting of Bucksport source rocks containing 20%biotite requires that fusion occurred at T860C and consumedall of the biotite in the source rock. Phase equilibrium dataand estimated temperatures of formation provide evidence thatthe granitoids formed at T<860C, whereas petrographic dataindicate that not all biotite in the source rock was consumedduring anatexis. Therefore, the WPC granitoids could have formedby fluid-absent melting if the source rocks contained >20%biotite (the maximum amount observed). However, it is also possiblethat influx of aqueous fluid before or during anatexis allowedproduction of relatively large volumes of melt at T<860C.Available data do not allow these possibilities to be rigorouslytested. The WPC granitoids have many characteristics of S-type granitesand preserve a chemical and mineralogical record of their sourcerocks, indicating that granites can image their sources evenin tectonically complex regions.     

Phase relationships in granulitic metapelites from the Ivrea-Verbano zone (Northern Italy)

Paragneisses of the Ivrea-Verbano zone exhibit over a horizontal distance of 5 km mineralogical changes indicative of the transition from amphibolite to granulite facies metamorphism. The most obvious change is the progressive replacement of biotite by garnet via the reaction: a $${\text{Biotite + sillimanite + quartz }} \to {\text{ Garnet + K - feldspar + H}}_{\text{2}} {\text{O}}$$ which results in a systematic increase in the modal ratio g = (garnet)/(garnet + biotite) with increasing grade. The systematic variations in garnet and biotite contents of metapelites are also reflected by the compositions of these phases, both of which become more magnesian with increasing metamorphic grade. The pressure of metamorphism has been estimated from the Ca₃Al₂Si₃O₁₂ contents of garnets coexisting with plagioclase, sillimanite and quartz. These phases are related by the equilibrium: b $$\begin{gathered} 3 CaAl_2 {\text{Si}}_{\text{2}} {\text{O}}_{\text{8}} \rightleftharpoons Ca_3 Al_2 {\text{Si}}_{\text{3}} {\text{O}}_{{\text{12}}} + 2 Al_2 {\text{SiO}}_{\text{5}} + {\text{SiO}}_{\text{2}} \hfill \\ plagioclase garnet sillimanite quartz \hfill \\ \end{gathered} $$ which has been applied to these rocks using the available data on the mixing properties of plagioclase and garnet solid solutions. Temperature and f _{H 2O} estimates have been made in a similar way using thermodynamic data on the biotite-garnet reaction (a) and the approximate solidus temperatures of paragneisses. Amphibolite to granulite facies metamorphism in the Ivrea-Verbano zone took place in the P-T ranges 9–11 kb and 700–820 °C. The differences in temperature and pressure of metamorphism between g= 0 and g = 1 (5 kms horizontal distance) were less than 50° C and approximately 1 kb. Retrogression and re-equilibration of garnets and biotites in the metapelites extended to temperatures more than 50° C below and pressures more than 1.5 kb below the peak of metamorphism, the degree of retrogression increasing with decreasing grade of the metamorphic “peak”. The pressure and temperature of the peak of metamorphism are not inconsistent with the hypothesis that the Ivrea-Verbano zone is a slice of upthrusted lower crust from the crust-mantle transition region, although it appears that the thermal gradient was too low for the zone to represent a near-vertical section through the crust. The most reasonable explanation of the granulite facies metamorphism is that it arose through intrusion of mafic rocks into a region already undergoing recrystallisation under amphibolite facies conditions.     

Dehydration Melting and Water-Saturated Melting of Basaltic and Andesitic Greenstones and Amphibolites at 1, 3, and 6. 9 kb

The melting relations of five metamorphosed basalts and andesites(greenstones and amphibolites), collected from the late JurassicSmartville arc complex of California, were investigated experimentallyat 800–1000? C and 1, 3, and 6. 9 kb. Dehydration-melting(no water added) experiments contained only the water structurallybound in metamorphic minerals (largely amphiboles). They yieldedmildly peraluminous to metaluminous granodioritic to trondhjemiticmelts (Na/K is a function of starting composition) similar inmajor element composition to silicic rocks in modern oceanicarcs. The dehydration melts are water-undersaturated, with,and coexist with the anhydrous residual solid (restite) assemblageplagioclase + orthopyroxene + clinopyroxene + magnetite ? ilmen-ite,with plagioclase constituting 50% of the restite mode. In thedehydration-melting experiments at 3 kb the onset of meltingoccurred between 850 and 900 ? C, as amphibole and quartz brokedown to yield pyroxenes plus melt. Total pressure is greaterthan in the dehydration-melting experiments and has little effecton melt composition or phase relations. In the water-saturated (water added, so that experiments, meltsformed at 3 kb and above are strongly peraluminous, rich inCa and poor in Fe, Mg, Ti, and K. Their compositions are unlikethose of most silicic igneous rocks. These melts coexist withthe amphibole-rich, plagioclase-poor restite assemblage amphibole+ magnetite ? clinopyroxene ? plagioclase ? ilmenite. The highlyaluminous nature of the melts and the plagioclase-poor natureof the restite both reflect the substantial contribution ofplagioclase (along with quartz) to melts in high-pressure water-saturatedsystems. Water pressure equals P_toul in the water-saturatedexperiments and has a profound effect on both melt compositionand phase relations. At 1 kb, the water-saturated experimentsyielded melt and mineral products with some characteristicsof the dehydration-melting experiments (no amphibole at highT), and some characteristics of the 3-kb, water-saturated experiments(amphibole plus melt coexisting at lower T, elevated Al, loweredFe). As pressure is increased from 3 to 6. 9 kb, the stabilityfields of both plagioclase and clinopyroxene decrease relativeto amphibole and the Al contents of the melts increase. These experiments have important implications for the petrogenesisof low-K silicic rocks in arcs. First, dehydration melting isa viable mechanism for the formation of these rocks; water-saturatedmelting is not. Second, because of the influence of rock compositionon melt composition, low-grade metamorphic and hydrothermalprocesses that alter the alkali contents and Na/ K in arc basementterranes may have a direct impact on the petrogenesis of silicicmagmas in arcs, particularly the formation of extremely low-Ktrondhjemites. Third, the experiments predict that anhydrous,pyroxene- and plagioclase-rich ‘granulitic’ restiteassemblages should develop as a result of partial melting inarc terranes. Such assemblages occur in at least two deeplyeroded arc complexes.     

Monazite as a monitor of melting,garnet growth and feldspar recrystallization in continental lower crust

Monazite is a common accessory phase in felsic granulite ribbon mylonites exposed in the Upper Deck domain of the Athabasca granulite terrane, western Canadian Shield. Field relationships, bulk rock geochemistry and phase equilibria modelling in the Na₂O–CaO–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–Fe₂O₃ system are consistent with the garnet‐rich rocks representing the residual products of ultrahigh temperature melting of biotite‐bearing paragneisses driven by intraplating of mafic magma in continental lower crust. The c. 2.64–2.61 Ga Y‐rich resorbed monazite cores included in garnet are interpreted as relicts of detrital grains deposited on the Earth's surface after c. 2.61 Ga. Yttrium‐poor monazite domains in garnet are depleted in Sm and Gd and linked to fluid‐absent melting of biotite + plagioclase + quartz ± sillimanite during a prograde loading path from ≤0.8 to ≥1.4 GPa. The c. 2.61–2.55 Ga Y‐depleted, Th‐rich monazite domains crystallized in the presence of garnet + ternary feldspar ± orthopyroxene + peraluminous melt. The c. 2.58–2.52 Ga monazite rims depleted in Th + Ca and enriched in Eu are linked to localized melt extraction synchronous with growth of high‐pressure (HP) grossular‐rich garnet at the expense of plagioclase during crustal thickening, culminating at >950 °C. Re‐heating and dextral transpressive lower crustal reactivation at c. 1.9 Ga resulted in syn‐kinematic growth of (La + Ce)‐enriched monazite and a second generation of garnet, concurrent with recrystallization of feldspar and orthopyroxene at 1.0–1.2 GPa and 600–700 °C. Monazite grains in this study are marked by positive Eu‐anomalies relative to chondrite. A direct link is implied between Y, Sm, Eu and Gd in monazite and two major phases in continental lower crust: garnet and plagioclase. Positive Eu‐anomalies in lower crustal monazite associated with modally abundant garnet appear to be directly related to Eu‐enrichment and depletions of Y, Sm and Gd that are consequences of garnet growth and plagioclase breakdown during HP melting of peraluminous bulk compositions.     

Oxygen isotopic study of Late Mesozoic cooling of the Mount Barcroft area,central White Mountains,eastern California

The Middle Jurassic Barcroft mafic granodiorite and Late Cretaceous, ternary-minimum McAfee Creek Granite are important components of the igneous arc sited along the SW North American margin. Bulk-rock analyses of 11 samples of the metaluminous, I-type Barcroft comagmatic suite have an average δ¹⁸O value of 7.4±0.6‰ (all values±1σ). Four Barcroft specimens average ε_Nd=?3.6±1.8, ⁸⁷Sr/⁸⁶Sr=0.707±0.001. The pluton consists of petrochemically gradational, Ca-amphibole-rich gabbro/diorite, granodiorite, metadiorite, and rare alaskite–aplite; for most of the pluton, oxygen isotope exchange of quartz, feldspar(s), biotite, and Ca-amphibole accompanied local deuteric alteration. Eight specimens of slightly peraluminous granitic rocks of the muscovite-bearing McAfee Creek series have an average δ¹⁸O of 8.6±0.5‰. Four McAfee-type samples average ε_Nd=?7.8±1.7, ⁸⁷Sr/⁸⁶Sr=0.711±0.004. For both plutons, bulk-rock evidence of exchange with near-surface water is lacking, suggesting ~5–10 km cooling depths. Barcroft minerals exhibit regular oxygen isotopic partitioning from high to low δ¹⁸O in the sequence quartz>plagioclase>K-feldspar>>amphibole≥biotite. Along the SE margin of the pluton, quartz and biotite in Lower Cambrian quartzites are higher in δ¹⁸O, and show slightly larger fractionations than igneous analogues. Exchange with fluids derived from these heated, contact-metamorphosed country rocks increased bulk ¹⁸O/¹⁶O ratios of Barcroft border rocks (and constituent plagioclase+subsolidus tremolite–actinolite), especially of granitic dikes transecting the wall rocks. Oxygen isotope thermometry for seven Barcroft pluton quartz–amphibole and six quartz–biotite pairs indicate apparent subsolidus temperatures averaging 519±49 °C. Quartz–plagioclase pairs from two Barcroft granodiorites yield values of 519 and 515 °C. A quartz–biotite pair from a quartzite adjacent to the Barcroft pluton yields an apparent temperature of 511 °C, in agreement with estimates based on contact metamorphic parageneses. Except for its SE margin, Barcroft pluton silicates evidently exchanged oxygen isotopes under local deuteric conditions. Compatible with Ca-amphibole thermobarometric analyses, areal distributions for quartz–plagioclase, quartz–amphibole, and quartz–biotite pairs reveal that putative annealing temperatures are lowest in NE-trending axial portions of the Barcroft body, so it simply cooled inwards. Intrusion ~70 million years later by the McAfee Creek Granite had no discernable effect on δ¹⁸O values of Barcroft minerals and bulk rocks.     

Pressure-temperature Evolution of the Metapelites in the Motuo Area,the Eastern Himalayan Syntaxis

The Motuo area is located in the east of the Eastern Himalayan Syntaxis. There outcrops a sequence of high-grade metamorphic rocks, such as metapelites. Petrology and mineralogy data suggest that these rocks have experienced three stages of metamorphism. The prograde metamorphic mineral assemblages(M1) are mineral inclusions(biotite + plagioclase + quartz ± sillimanite ± Fe-Ti oxides) preserved in garnet porphyroblasts, and the peak metamorphic assemblages(M2) are represented by garnet with the lowest XSps values and the lowest XFe# ratios and the matrix minerals(plagioclase + quartz ± Kfeldspar + biotite + muscovite + kyanite ± sillimanite), whereas the retrograde assemblages(M3) are composed of biotite + plagioclase + quartz symplectites rimming the garnet porphyroblasts. Thermobarometric computation shows that the metamorphic conditions are 562–714°C at 7.3–7.4 kbar for the M1 stage, 661–800°C at 9.4–11.6 kbar for the M2 stage, and 579–713°C at 5.5–6.6 kbar for the M3 stage. These rocks are deciphered to have undergone metamorphism characterized by clockwise P-T paths involving nearly isothermal decompression(ITD) segments, which is inferred to be related to the collision of the India and Eurasia plates.     

Distribution of REE,LILE, and HFSE between biotite,feldspar, and the melt in the granulite facies migmatite,nimnyr block,Aldan shield

The behavior of trace elements under conditions of partial melting of granitoid rocks has been studied. The element’s partition coefficients between minerals and the melt D_i^min/melt depends, in the first place, on the composition of the primary melt. In biotite the HREE D_i are a little below 1, while those of LREE, especially D_i for Ce, are 1–3 orders of magnitude less. This leads to an efficient differentiation of REEs in anatexic melts especially when biotite is the main mineral phase of restite. On the contrary, there are feldspars, the D_i of which cannot provide such a magnitude of differentiation. Unlike garnets and pyroxenes, whose stability in restite permits enrichment of anatexic melts produced in migmatization zones with Nb, Ti, and Cr, the presence of biotite in restite causes depletion of melts with those elements as well as with Rb. Feldspars, under conditions of their fractional crystallization or during differentiation of an anatexic melt, deplete the latter with Sr, Ba, and Rb, but enrich it with Nb, Ti, Cr, Y, Zr, and V.     

On the interpretation of peak metamorphic temperatures in light of garnet diffusion during cooling

Abstract Finite difference models of Fe-Mg diffusion in garnet undergoing cooling from metamorphic peak conditions are used to infer the significance of temperatures calculated using garnet-biotite Fe-Mg exchange thermometry. For rocks cooled from high grades where the garnet was initially homogeneous, the calculated temperature (T_calc) using garnet core and matrix biotite depends on the size of the garnet, the ratio of garnet to biotite in the rock (V_garnet/V_biotite) and the cooling rate. For garnets with radii of 1 mm and V_garnet/V_biotite<1, T_calc is 633, 700 and 777°C for cooling rates of 1, 10 and 100°C/Ma. For V_garnet/V_biotite= 1 and 4 and a cooling rate of 10° C/Ma, T_calc is approximately 660 and 610° C, respectively. Smaller and larger garnets have lower and higher T_calc, respectively. These results suggest that peak metamorphic temperatures may be reliably attained from rocks crystallized at conditions below T_calc of the garnet core, provided that V_garnet/V_biotite is sufficiently small (<0.1) and that the composition of the biotite at the metamorphic peak has not been altered during cooling. Numerical experiments on amphibolite facies garnets with nominal peak temperatures of 550–600° C generate a ‘well’in Fe/(Fe + Mg) near the rim during cooling. Maximum calculated temperatures for the assemblage garnet + chlorite + biotite + muscovite + plagioclase + quartz using the Fe/(Fe + Mg) at the bottom of the ‘well’with matrix biotite range from 23–43° C to 5–12° C below the peak metamorphic temperature for cooling rates of 1 and 100° C/Ma, respectively. Maximum calculated temperatures for the assemblage garnet + staurolite + biotite + muscovite + plagioclase + quartz are approximately 70° C below the peak metamorphic temperature and are not strongly dependent on cooling rate. The results of this study indicate that it may be very difficult to calculate peak metamorphic temperatures using garnet-biotite Fe-Mg exchange thermometry on amphibolite facies rocks (T_max > 550° C) because the rim composition of the garnet, which is required to calculate the peak temperature, is that most easily destroyed by diffusion.     

Calcic amphibole equilibria and a new amphibole-plagioclase geothermometer

There is currently a dearth of reliable thermobarometers for many hornblende and plagioclase-bearing rocks such as granitoids and amphibolites. A semi-empirical thermodynamic evaluation of the available experimental data on amphibole+plagioclase assemblages leads to a new thermometer based on the Al^iv content of amphibole coexisting with plagioclase in silica saturated rocks. The principal exchange vector in amphiboles as a function of temperature in both the natural and experimental studies is \(\left( {Na\square _{ - 1} } \right)^A \left( {AlSi_{ - 1} } \right)^{T1}\) . We have analysed the data using 3 different amphibole activity models to calibrate the thermometer reactions 1. $$1. Edenite + 4 Quartz = Tremolite + Albite$$ 2. $$2. Pargasite + 4 Quartz = Hornblende + Albite.$$ The equilibrium relation for both (1) and (2) leads to the proposed new thermometer $$T = \frac{{0.677P - 48.98 + Y}}{{ - 0.0429 - 0.008314 ln K}} and K = \left( {\frac{{Si - 4}}{{8 - Si}}} \right)X_{Ab}^{Plag} ,$$ where Si is the number of atoms per formula unit in amphiboles, with P in kbar and T in K; the term Y represents plagioclase non-ideality, RTlnγ_ab, from Darken's Quadratic formalism (DQF) with Y=0 for X _ab>0.5 and Y=-8.06+25.5(1-X _ab)² for X _ab<0.5. The best fits to the data were obtained by assuming complete coupling between Al on the T1 site and Na in the A site of amphibole, and the standard deviation of residuals in the fit is ±38°C. The thermometer is robust to ferric iron recalculation procedures from electron probe data and should yield temperatures of equilibration for hornblende-plagioclase assemblages with uncertainties of around ±75° C for rocks equilibrated at temperatures in the range 500°–1100° C. The thermometer should only be used in this temperature range and for assemblages with plagioclase less calcic than An₉₂ and with amphiboles containing less than 7.8 Si atoms pfu. Good results have been attained on natural examples from greenschist to granulite facies metamorphic rocks as well as from a variety of mafic to acid intrusive and extrusive igneous rocks. Our analysis shows that the pressure dependence is poorly constrained and the equilibria are not suitable for barometry.     

Genesis of the Katugin rare-metal ore deposit: Magmatism versus metasomatism

Arguments in favor of magmatic or metasomatic genesis of the Katugin rare-metal ore deposit are discussed. The geological and mineralogical features of the deposit confirm its magmatic origin: (1) the shape of the ore-bearing massif and location of various types of granites (biotite, biotite–amphibole, amphibole, and amphibole–aegirine); (2) the geochemical properties of the massif rocks corresponding to A type granite (high alkali content (up to 12.3% Na₂O + K₂O), extremely high FeO/MgO ratio (f = 0.96–1.00), very high content of the most incoherent elements (Rb, Li, Y, Zr, Hf, Ta, Nb, Th, U, Zn, Ga, and REE) and F, and low concentrations of Ca, Mg, Al, P, Ba, and Sr); (3) Fe–F-rich rock-forming minerals; (4) no previously proposed metasomatic zoning and regular replacement of rock-forming minerals corresponding to infiltration fronts of metasomatism. The similar ages of the barren (2066 ± 6 Ma) and ore-bearing (2055 ± 7 Ma) granites along with the features of the ore mineralization speak in favor of the origin of the ore at the magmatic stage of the massif’s evolution. The nature of the ore occurrence and the relationships between the ore minerals support their crystallization from F-rich aluminosilicate melt and also under melt liquation into aluminosilicate and fluoride (and/or aluminofluoride) fractions.     

Metamorphism of the Basement of the Qilian Fold Belt in the Minhe-Ledu Area, Qinghai Province, NW China

The basement of the central Qilian fold belt exposed along the Minhe-Ledu highway consists of psammitic schists, metabasitic rocks, and crystalline limestone. Migmatitic rocks occur sporadically among psammitic schist and metabasitic rocks. The mineral assemblage of psammitic schist is muscovite + biotite + feldspar + quartz ± tourmaline ± titanite ± sillimanite and that of metabasitic rocks is amphibole + plagioclase + biotite ± apatite ± magnetite ± pyroxene ± garnet ± quartz. The migmatitic rock consists of leucosome and restite of various volume proportions; the former consists of muscovite + alkaline feldspar + quartz ± garnet ± plagioclase while the latter is either fragments of psammitic schist or those of metabasitic rock. The crystalline limestone consists of calcite that has been partly replaced by olivine. The olivine was subsequently altered to serpentine. Weak deformations as indicated by cleavages and fractures were imposed prominently on the psammitic schists, occasionally on me     

Petrogenesis of the Kinsman Intrusive Suite: Peraluminous Granitoids of Western New Hampshire

The Kinsman Intrusive Suite occurs in six major plutons of westernNew Hampshire, covering a total area of 2240 km². It is an Acadian-agesyntectonic gneissic S-type peraluminous granitoid, rangingin composition from quartz diorite to granite. Much of the Kinsmanis characterized by very large (up to 120 mm in maximum dimension)megacrysts of alkali feldspar, but the bulk chemistry of therocks indicates that these cannot be phenocrysts crystallizedfrom initially homogeneous melts. Locally, there is abundant(20 per cent) almandine-rich garnet, and graphite is a commonaccessory.In contrast to the unannealed orthoclase in surroundingmetapelites, the alkali feldspar of the Kinsman has, for themost part, inverted to maximum microcline. The garnets havecore temperatures in the range of 800 to 900 ?C, and are pseudomorphedby, or show reaction rims to, biotite. Plagioclase commonlyshows zoning, some of it oscillatory. These features are magmaticin nature, and argue against the conclusions of previous investigatorsthat the mineralogy and textures of the rock are due to regionalmetamorphism of a previously-crystallized two-mica granitoidwhich has undergone prograde reactions such as:muse + bio +3 qtz 2 Kfs + gar + 2H₂O.The intrusives have also producedrecognizable contact-metamorphic features in the wallrocks andare probably coeval with the dominant M2 Acadian metamorphism.Majorelement analytical data for the Kinsman suite has been examinedby least squares mixing-model and extended Q-mode factor analysis.These calculations, supported by consideration of REE data,suggest that the most likely origin for the Kinsman magmas isby deep-crustal anatexis of slightly calcareous metapelites,and involves a reaction such as:bio + Al₂SiO₅ + qtz + feldspars gar + cord + Kfs + plag + melt.In non-calcareous pelites thisreaction produces a water-undersaturated peraluminous melt attemperatures above 700 ?C, and allows for the early crystallizationor recrystallization of K-feldspar, plagioclase, and garnetin a crystal-liquid mush or migma. Geochemically, garnet + plagioclaseare treated as restite, and a minimum-melt granite as the magmain the Q-mode and mixing-model calculations. The variabilityin chemistry of the Kinsman Intrusive Suite is best explainedon the basis of mixing of leucogranitic anatectic melts withgarnet-plagioclase restitic material and a quartz-feldspar-sillimanite-biotiterock, but only very slightly affected by crystal settling.     

Experimental investigation of the formation of cordierite-orthopyroxene parageneses in pelitic rocks

Cordierite and orthopyroxene (or orthoamphibole) are widespread in migmatitic terranes, and partial melting of pelitic rocks may be important in their production. In particular, the reaction quartz +albite+biotite+garnet+water vapor = cordierite +orthopyroxene or orthoamphibole+melt was among reactions discussed by Grant (1973) but poorly constrained in pressure-temperature space.This reaction involves too many phases to be readily studied experimentally. Therefore simpler melting and dehydration reactions involving quartzalbite-biotite-cordierite-orthopyroxene were investigated.In conjunction with the work of Hoffer (1976, 1978) these experiments place useful constraints on the above reaction and on the reaction quartz+albite+aluminosilicate+biotite+vapor = cordierite+garnet+melt. In pelitic rocks near the second illimanite isograd, cordierite and garnet may coexist with melt as low as 660° C and cordierite and orthopyroxene may coexist with melt at temperatures less than 675° C. In the absence of significant Mn or Ca, in pelitic rocks within the realm of melting, biotite+garnet assemblages are probably limited to pressures greater than 2kb and aluminosilicate+biotite assemblages to pressures greater than 3kb.     

Retrograde formation of NaCl-scapolite in high pressure metaevaporites from the Cordilleras Béticas (Spain)

A Permo-Triassic pelite-carbonate rock series (with interacalated metabasitic rocks) in the Cordilleras Béticas, Spain, was metamorphosed during the Alpine metamorphism at high pressures (P _min near 18 kbar). The rocks show well preserved sedimentary features of evaporites such as pseudomorphs of talc, of kyanite-phengitetalc-biotite, and of quartz after sulfate minerals, and relicts of baryte, anhydrite, NaCl, and KCl, indicating a salt-clay mixture of illite, chlorite, talc, and halite as the original rock. The evaporitic metapelites have a whole rock composition characterized by high Mg/(Mg+Ca) ratios>0.7, variable alkaline and Sr, Ba, contents, but are mostly K₂O rich (<8.8 wt%). The F (<2600 ppm), Cl (<3600 ppm), and P₂O₅ (<0.24 wt%) contents are also high. The pelitic member of this series is a fine grained biotite rock. Kyanite-phengite-talc-biotite aggregates in pseudomorphs developed in the high pressure stage. Albite-rich plagioclase was formed when the rocks crossed the albite stability curve in the early stages of the uplift. Scapolite, rich in NaCl (Ca/(Ca+Na) mol% 24–40) and poor in SO₄, with Cl/(Cl+CO₃) ratios between 0.6 and 0.8, formed as porphyroblasts, sometimes replacing up to 60% of the rock in a late stage of metamorphism (between 10 and 5 kbar, near 600°C). No reaction with albite is observed, and the scapolite formed from biotite by: $$\begin{gathered} Al - biotite + CaCO_3 + NaCl + SiO_2 \hfill \\ = Al - poor biotite + scapolite + MgCO_3 + KCl \hfill \\ + MgCl_2 + H_2 O \hfill \\ \end{gathered}$$ Calculated fluid composition in equilibrium with scapolite indicates varying salt concentrations in the fluid. Distribution of Cl and F in biotite and apatite also indicates varying fluid compositions.     

Neoproterozoic magmatism in NW Sinai,Egypt: magma source and evolution of collision-related intracrustal anatectic leucogranite

The present study deals with tectonomagmatic evolution of the collision-related leucogranite located near the northwest corner of exposed basement in Sinai, Egypt. The area is composed of: (1) a gabbroic complex; (2) amphibolite; (3) post-orogenic leucogranite; (4) Feiran gneisses. The amphibolite and gabbroic suites, generated in an island arc environment, have a high Fe-tholeiitic affinity and were derived from two independent magmas. On the basis of rare earth element (REE) patterns, the gabbroic melts could have been generated from a garnet- and amphibole-bearing, enriched mantle, and were subsequently modified by fractional crystallization of pyroxene and amphibole with minor plagioclase, whereas the amphibolite melts could be derived from garnet-free depleted mantle.The leucogranite has high Al₂O₃ content (>13 wt%), alumina saturation index (ASI) mostly >1, and normative corundum, indicating a peraluminous nature. Chondrite-normalized REE patterns for the leucogranite show light REE enrichment (La/Sm_N=2.7–4.86), general flattening of the heavy REE (Gd/Lu_N=1.2–2), and negative europium (Eu) anomalies (Eu/Eu*=0.24–0.47). The peraluminous nature and enrichment of the incompatible elements (K, Rb, Ba and Th) in the leucogranite strongly suggest derivation from a crustal source. The most probable source for the leucogranite magmas is represented by the adjacent Feiran gneisses, which could have generated the leucogranite by dehydration melting under water-undersaturated conditions. It appears likely that the restite unmixing model is responsible for the chemical variations within the leucogranite. In accordance with this model, the chemical variation of the leucogranite can be attributed to varying degrees of separation of restitic material from the melt during its emplacement and solidification and fractional crystallization could have played a minor role during magma ascent through the crust.     

Origin of biotite-hornblende-garnet coronas between oxides and plagioclase in olivine metagabbros,Adirondack region,New York

Complex multivariant reactions involving Fe-Ti oxide minerals, plagioclase and olivine have produced coronas of biotite, hornblende and garnet between ilmenite and plagioclase in Adirondack olivine metagabbros. Both the biotite (6–10% TiO₂) and the hornblende (3–6% TiO₂) are exceptionally Titanium-rich. The garnet is nearly identical in composition to the garnet in coronas around olivine in the same rocks. The coronas form in two stages:

1. Plagioclase+Fe-Ti Oxides+Olivine+water =Hornblende+Spinel+Orthopyroxene±Biotite +more-sodic Plagioclase
2. Hornblende+Orthopyroxene±Spinel+Plagioclase =Garnet+Clinopyroxene+more-sodic Plagioclase

The Orthopyroxene and part of the clinopyroxene form adjacent to olivine. Both reactions are linked by exchange of Mg²⁺ and Fe²⁺ with the reactions forming pyroxene and garnet coronas around olivine in the same rocks. The reactions occur under granulite fades metamorphic conditions, either during isobaric cooling or with increasing pressure at high temperature.     

Partial melting of metagreywackes, Part II. Compositions of minerals and melts

A series of experiments on the fluid-absent melting of a quartz-rich aluminous metagreywacke has been carried out. In this paper, we report the chemical composition of the phases present in the experimental charges as determined by electron microprobe. This analytical work includes biotite, plagioclase, orthopyroxene, garnet, cordierite, hercynite, staurolite, gedrite, oxide, and glass, over the range 100–1000 MPa, 780–1025 °C. Biotites are Na- and Mg-rich, with Ti contents increasing with temperature. The compositions of plagioclase range from An₁₇ to An₃₅, with a significant orthoclase component, and are always different from the starting minerals. At high temperature, plagioclase crystals correspond to ternary feldspars with Or contents in the range 11–20 mol%. Garnets are almandine pyrope grossular spessartine solid solutions, with a regular and significant increase of the grossular content with pressure. All glasses are silicic (SiO₂ = 67.6–74.4 wt%), peraluminous, and leucocratic (FeO + MgO = 0.9–2.9 wt%), with a bulk composition close to that of peraluminous leucogranites, even for degrees of melting as high as 60 vol.%. With increasing pressure, SiO₂ contents decrease while K₂O increases. At any pressure, the melt compositions are more potassic than the water-saturated granitic minima. The H₂O contents estimated by mass balance are in the range 2.5–5.6 wt%. These values are higher than those predicted by thermodynamic models. Modal compositions were estimated by mass balance calculations and by image processing of the SEM photographs. The positions of the 20 to 70% isotects (curves of equal proportion of melt) have been located in the pressure-temperature space between 100 MPa and 1000 MPa. With increasing pressure, the isotects shift toward lower temperature between 100 and 200 MPa, then bend back toward higher temperature. The melting interval increases with pressure; the difference in temperature between the 20% and the 70% isotects is 40 °C at 100 MPa, and 150 °C at 800 MPa. The position of the isotects is interpreted in terms of both the solubility of water in the melt and the nature of the reactions involved in the melting process. A comparison with other partial melting experiments suggests that pelites are the most fertile source rocks above 800 MPa. The difference in fertility between pelites and greywackes decreases with decreasing pressure. A review of the glass compositions obtained in experimental studies demonstrates that partial melting of fertile rock types in the crust (greywackes, pelites, or orthogneisses) produces only peraluminous leucogranites. More mafic granitic compositions such as the various types of calk-alkaline rocks, or mafic S-type rocks, have never been obtained during partial melting experiments. Thus, only peraluminous leucogranites may correspond to liquids directly formed by partial melting of metasediments. Other types of granites involve other components or processes, such as restite unmixing from the source region, and/or interaction with mafic mantle-derived materials. Received: 11 July 1995 / Accepted: 27 February 1997     

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.     

Solubility of excess alumina in hydrous granitic melts in equilibrium with peraluminous minerals at 700–800 °C and 200 MPa,and applications of the aluminum saturation index

We have studied the controls on the Aluminum Saturation Index (ASI = molec. Al₂O₃/[(CaO)+(Na₂O)+(K₂O)]) and the concentration of normative corundum of granitic liquids saturated in alumina by equilibrating peraluminous minerals with initially metaluminous haplogranitic minimum composition liquids at 700–800 °C and 200 MPa, at, and below H₂O saturation. The ASI and normative corundum increase with increasing H₂O concentration in the melt (0.04 to 0.10 moles excess Al₂O₃ per mole of H₂O), temperature, and with addition of the non-haplogranitic components Fe, Mg, and B. The ASI parameter and concentration of normative corundum cannot be used to monitor aAl₂O₃ between different mineral assemblages and melt because other components that affect the solubility of alumina, including H₂O, Fe, Mg, and B, do not appear in their formulations. ASI and normative corundum, however, provide petrogenetic information about magmas generated by partial melting of strongly peraluminous protoliths by virtue of their regular and predictable variation with melt composition (e.g., H₂O concentration) and temperature. For the application of these data to natural rocks it is necessary to choose as an analogue system the ASI-solubility or normative corundum-solubility relations of the most chemically complex peraluminous mineral present in the rock. Comparison of ASI values of anatectic leucosomes and allochthonous leucogranites with experimentally predicted values suggests low H₂O concentrations in melt during crustal partial melting. Rapid melt segregation before equilibration with restitic peraluminous phases is also suggested in some cases.Editorial responsibility: I. Carmichael