The influence of crystallography and kinetics on phengite breakdown reactions in a low-pressure metamorphic aureole

A natural example of phengite that had undergone partial thermal decomposition at a pressure of about 0.5 kbar and a temperature of about 680° C in a contact aureole was exmined in the transmission electron microscope (TEM). Partially pseudomorphed phengites were found to consist of combinations of phengite, biotite, K-feldspar, mullite, sillimanite, spinel and cordierite. Different areas within individual, partially pseudomorphed, phengite grains show various degrees of reaction and different reaction products; the cores are the least reacted and the margins have reacted most. In the cores the assemblage Al-, Mg-enriched phengite+biotite +K-feldspar+mullite±spinel has formed, whereas the assemblage K-feldspar+mullite+sillimanite+spinel +biotite+cordierite has formed at the edges. According to our thermodynamic calculations, the breakdown of phengite should have produced cordierite+spinel +corundum+K-feldspar in regions isolated from the influx of SiO₂ and cordierite+andalusite+quartz+K-feldspar in regions near the edge of the grains that were essentially saturated with SiO₂. Chemical equilibrium was not achieved in any part of the partially pseudomorphed phengites on a micron scale or larger. Breakdown theoretically should have been complete by about 550° C; the reaction temperature was overstepped by at least 130° C for 20–25 years. The variations in the degree and type of reaction are probably due partly to the availability of suitable nucleation sites in different regions, partly to the need to remove H₂O from reaction sites and partly to the influence of SiO₂, which diffused into the grains during metamorphism. The presence of SiO₂ lowers the equilibrium temperatures. Thus there is a higher driving force for breakdown near the grain boundaries than in the cores. Most of the products show an orientation relationship with the parent phengite and have consistent habit planes; they have their closest-packed planes and closest-packed directions parallel to one another and to those of phengite. Such relationships minimize the strain and surface energies at nucleation and favour most rapid nucleation and growth of the reaction products. The great structural similarity of biotite to phengite resulted in its having the highest rate of nucleation and growth of any product and it occurred in all areas of the phengite pseudomorphs studied. Mullite and sillimanite were produced metastably. Mullite has more rapid nucleation kinetics than other aluminosilicates because it is structurally disordered. Sillimanite formed rather than andalusite in regions of the partially pseudomorphed phengites where the reaction reached an advanced stage, because the reaction from phengite to andalusite requires an energetically unfavourable change in aluminium co-ordination state.     

Si+4 Content of natural phengites

The chemical compositions of white micas separated from adjacent rocks of glaucophane and greenschist facies are compared with respect to their Si⁺⁴ content. The micas are predominantly phengitic, i.e. between muscovite, K[Al₂Si₃AlO₁₀(OH)₂] and celadonite, K[(R⁺²R⁺³)Si₄O₁₀(OH)₂] in composition. Constancy of Si content in micas coming from rocks of different bulk chemical composition but closely similar physical conditions indicates that the silica content of a potassic dioctahedral mica can be used to indicate the pressure and temperature conditions of its formation. This conclusion is in part based upon previous experimental data obtained for synthetic phengites.     

Jadeitites, albitites and related rocks from the Motagua Fault Zone, Guatemala

Jadeitites from Guatemala are found as weathered blocks in tectonized serpentinite in a 15-km zone north of the Motagua Fault Zone. Rock types found with jadeitite include albitites, albite-mica rocks, omphacite/taramitic amphibole-bearing metabasites, chlorite-actinolite schists, talc-carbonate rocks and antigorite schists. In addition to the predominant jadeitic (Jd₉₃_₁₀₀) pyroxene, common phases in jadeitite include micas (paragonite and/or phengite ± rarer phlogopite), omphacite, albite, titanite /Pm zircon, apatite and graphite. Conditions of jadeitite formation are 100-400d? C, 5-11 kbar with 0.0 > log₁₀a_sio2≥= 0.7. Fluid inclusions, coarse textures, vein structures, and rhythmic zoning of pyroxene indicate an aqueuos fluid was involved. Jadeitites are either (1) metasomatic modifications of former felsic-to-pelitic inclusions that have undergone silica depletion plus efficient soda exchange and enrichment, or (2) solution precipitations derived from such a source. The close spatial relationship of faults and shear zones, serpentinites, and jadeitites suggests jadeitites form in a relatively high-P/T setting with substantial flow of sodic fluid in a tectonized zone. Most Guatemalan jadeitites are extensively altered to analcime, albite, taramitic amphibole, (clino)zoisite ± nepheline and preiswerkite. This alteration reflects depressurization /Pm heating to below the jadeite + fluid = analcime reaction at high a_Na. With progressive alteration, analcime and nepheline are replaced by albite; the increase in silica content may result from fluid flowing up a tectonized zone reaching saturation with an albite assemblage. Albitite phases, albite, actinolite, zoisite, /Pm chlorite, phengite, K-feldspar and quartz, record conditions of c. 3-8 kbar at T < 400d? C, indicating a clockwise P-T trajectory of the blocks. Barium aluminosilicates—banalsite, celsian, cymrite and hyalophane—are common minor late-stage phases in jadeitites and albite-rich rocks. Barian phengite is common in albite-mica rocks.     

40Ar/39Ar dating of white micas from an Alpine high-pressure metamorphic belt on Naxos (Greece): the resetting of the argon isotopic system

Overprinting of white micas from high pressure, low to medium temperature (M ₁) metamorphic assemblages in pelitic schists on Naxos during subsequent thermal dome (M ₂) metamorphism ranges from minor in the southeast of the island to complete recrystallization in the amphibolite facies rocks near the migmatites in the centre of the dome. The original (M ₁) minerals are phengites (Si⁴⁺=6.7–7.0) and the overprinting minerals are muscovites (Si⁴⁺=6.0–6.45). ⁴⁰Ar/³⁹Ar step heating analyses of white mica separates from rocks in the area where phengite and muscovite occur together yield complex age spectra, characterized by low apparent ages in the first and the last stages of gas release and high apparent ages in between. These upward-convex age spectra are shown to be caused by mixing of two generations of micas, each of which has a different age spectrum and argon release pattern. Seemingly good plateaus in some age spectra from white micas of the area must be interpreted as providing meaningless intermediate ages. Further, the upward-convex age spectra have been used to trace the isotopic signature of phengites toward increasing M ₂ metamorphic grade, and suggest that as long as phengites can be observed in the rocks upward-convex age spectra occur. On Naxos, crystallization of muscovite at the expense of phengite appears to be the main mechanism of resetting argon isotopic ages in white micas. However, there is also good evidence for argon loss by volume diffusion from phengites. Simple diffusion calculations suggest that the M ₂ metamorphism was caused by a shortlived heat source.Now at Department of Geology, University of Alberta, Edmonton T6G 2E3, Canada     

The mineral chemistry,near-infrared,and mid-infrared reflectance spectroscopy of phengite from the Olympic Dam IOCG deposit,South Australia

Phengite is the main potassic dioctahedral mica identified at the Olympic Dam iron oxide–copper–gold (IOCG) deposit, South Australia, where its mineral chemistry is quite variable. These differences can be explained by contrasting degrees of hydrothermal alteration. In the heavily-sericitized, ore-bearing rocks, the phengites display a lower-Si content, a higher-Al content, and a lower Mg-number than the phengites from the weakly-sericitized alteration halo that surrounds the deposit. Variations are also observed in the near- and mid-infrared reflectance spectra collected from phengite-bearing rocks. In the near-infrared, high-Al phengite produces a spectral absorption feature at 2.206 μm, and this feature is displaced to 2.213 μm for low-Al phengite. In the mid-infrared, high-Al phengite produces a strong reflectance peak at 9.59 μm, whereas this peak is observed at 9.57 μm in the spectra from low-Al phengite. Additional peaks were also identified at 10.98, 12.22, and 13.33 μm. These were most intense in the spectra from high-Al phengite. A drill core profile was produced using the results of the spectral analysis that shows the change in phengite mineral chemistry and phengite abundance as a function of depth. In general, near- and mid-infrared reflectance spectroscopy can be used to characterize the aluminum content of potassic dioctahedral micas like phengite, and this information can be used to infer the degree of sericitic alteration that has occurred as a result of hydrothermal fluid flow.     

Application of K-feldspar–jadeite–quartz barometry to eclogite facies metagranites and metapelites in the Sesia Lanzo Zone (Western Alps, Italy)*

The eclogite facies assemblage K-feldspar–jadeite–quartz in metagranites and metapelites from the Sesia-Lanzo Zone (Western Alps, Italy) records the equilibration pressure by dilution of the reaction jadeite+quartz=albite. The metapelites show partial transformation from a pre-Alpine assemblage of garnet (Alm₆₃Prp₂₆Grs₁₀)–K-feldspar–plagioclase–biotite±sillimanite to the Eo-Alpine high-pressure assemblage garnet (Alm₅₀Prp₁₄Grs₃₅)–jadeite (Jd_80–97Di_0–4Hd_0–8Acm_0–7)–zoisite–phengite. Plagioclase is replaced by jadeite–zoisite–kyanite–K-feldspar–quartz, and biotite is replaced by garnet–phengite or omphacite–kyanite–phengite. Equilibrium was attained only in local domains in the metapelites and therefore the K-feldspar–jadeite–quartz (KJQ) barometer was applied only to the plagioclase pseudomorphs and K-feldspar domains. The albite content of K-feldspar ranges from 4 to 11 mol% in less equilibrated assemblages from Val Savenca and from 4 to 7 mol% in the partially equilibrated samples from Monte Mucrone and the equilibrated samples from Montestrutto and Tavagnasco. Thermodynamic calculations on the stability of the assemblage K-feldspar–jadeite–quartz using available mixing data for K-feldspar and pyroxene indicate pressures of 15–21 kbar (±1.6–1.9 kbar) at 550±50 °C. This barometer yields direct pressure estimates in high-pressure rocks where pressures are seldom otherwise fixed, although it is sensitive to analytical precision and the choice of thermodynamic mixing model for K-feldspar. Moreover, the KJQ barometer is independent of the ratio PH2O/P_T. The inferred limiting a(H₂O) for the assemblage jadeite–kyanite in the metapelites from Val Savenca is low and varies from 0.2 to 0.6.     

Zoning and recrystallization of phengitic micas: implications for metamorphic equilibration

White micas (phengites) in the metasediments of the Scottish Dalradian display a large range of compositions within single samples. The variations in the composition of these phengites are strongly controlled by their structural age, with early fabrics containing a paragonite-poor, celadonite-rich phengite whereas in later fabrics the micas are generally paragonite-rich and celadonite-poor. Retrograde phengite growth, identified using back scattered electron imaging, occurs as celadonite-rich rims on micas within all existing fabrics and appears to be preferentially developed along existing white mica-plagioclase grain boundaries. The presence of these chemically distinct phengite populations within single samples implies that chemical exchange between the individual micas was inefficient. It is proposed that diffusion-controlled exchange reactions in phengites have relatively high closure temperatures below which major element exchange is effectively impossible. This closed system behaviour of micas questions the ease with which phengites may equilibrate with other phases during prograde greenschist and lower amphibolite facies metamorphism. Many of the chemical variations preserved in phengites from such metamorphic rocks may reflect deformation/recrystallization controlled equilibria.     

K-rich fluid metasomatism at high-pressure metamorphic conditions: Lawsonite decomposition in rodingitized ultramafite of the Maksyutovo Complex, Southern Urals (Russia)

Fine grained rodingite‐like rocks containing epidote, clinozoisite, garnet, chlorite, phengite and titanite occur within antigorite serpentinite boudins from the high‐pressure metamorphic Maksyutovo Complex in the Southern Urals. Pseudomorphs after lawsonite, resorption of garnet by chlorite and phengite and stoichiometry suggest the reaction lawsonite + garnet + K‐bearing fluid → clinozoisite + chlorite + phengite, and define a relic assemblage of lawsonite + garnet + chlorite + titanite ± epidote as well as a later post‐lawsonite assemblage of clinozoisite + phengite + chlorite + titanite. The reaction lawsonite + titanite → clinozoisite + rutile + pyrophyllite + H₂O delimits the maximum stability of former lawsonite + titanite to pressures >13 kbar. P–T conditions of 18–21 kbar/520–540 °C result, if the average chlorite, Mg‐rich garnet rim and average epidote compositions are used as equilibrium compositions of the former lawsonite assemblage. These estimates indicate a similar depth of formation but lower temperatures to those recorded in nearby eclogites. The metamorphic conditions of the lawsonite assemblage are considerably higher than previously suggested and, together with published structural data, support a model in which a normal fault within the Maksyutovo complex acted as the major transport plane of eclogite exhumation. The maximum Si content of phengite and minimum Fe content in clinozoisite constrain the metamorphic conditions of the later pseudomorph assemblage to be >4.5 kbar and <440 °C. Rb–Sr isotopic dating of the pseudomorph assemblage results in a formation age of 339 ± 6 and 338 ± 5 Ma, respectively. These results support the recent exhumation models for this complex.     

Succession de subfacies métamorphiques en Vanoise méridionale (Savoie)

The Southern Vanoise is localized in the internal part of the Western Alps, in the Briançonnais zone. In Vanoise the following units can be distinguished (Fig. 1): a pre-hercynian basement (micaschists, glaucophanites, basic rocks), a permian cover (micaschists) and a mesozoic-paleocene cover (carbonate rocks). This area has been affected by the alpine metamorphic event characterized here by high and intermediate pressure facies. The rocks paragenesis are often unbalanced.The paleozoic rocks (Table 1) contain mainly: quartz, albite, paragonite, phengite, blue amphibole, chlorite, green biotite, garnet (Table 2). These minerals were analysed by an electron microprobe (Tables 3, 4 and 5). Mineral composition is highly variable: glaucophane is zoned (Table 5), white micas are more or less substituted with phengite (3.22O₃/FeO + MgO)<0.53] whereas the Al rich chlorites [(Al₂O₃/FeO + MgO)>0.6] are associated with the less substituted white micas (Si=3.2) (Tables 3 and 4). The phengites with a Si content 3.2 occur in rocks where the retromorphic evolution is the most pronounced and penetrative. A metamorphic evolution is characterized by the disappearance of glaucophane which corresponds to the appearance of Al rich chlorite and to the decrease of phengitic substitution.The samples analysis are plotted in the tetraedric diagram: K₂O-Al₂O₃-Na₂O, Al₂O₃-FeO, MgO, on which a special mathematical treatment was applied. This method calculates the location of rocks composition in the four minerals space. This location is internal when the per cent amounts of all four relevant minerals are positive, if any of them is negative, the point is external (Tables 6–9).In Southern Vanoise micaschists, 2 subfacies are successively present (Fig. 3):Subfacies I: glaucophane-chlorite-phengite (Si⁴⁺ 3.5)-paragonite. Then subfacies II: chlorite-albite-phengite (Si⁴⁺ 3.2)-paragonite.In basic rocks is found essentially: Subfacies III: glaucophane-garnet-phengite-paragonite or IV: glaucophane-garnet-phengite-albite. Then subfacies V: green biotite-chlorite-albite-paragonite.The assemblages I and II proceed through reaction: 2 glaucophane +1 paragonite+2 H₂O4.2 albite + 1 chlorite.The assemblage V appears with reactions: 1.8 glaucophane +2 phengite0.4 chlorite+2 green biotite + 3.6 albite +0.4 H₂O or 2 glaucophane +2 phengite +0.5 garnet+ 6 H₂O2 green biotite +1 chlorite+4 albiteThese reactions are controlled by hydratation: the composition variation of phengite and associated chlorite during the metamorphic evolution determines the stability of some minerals (particularly the glaucophane in Na₂O poor rocks).In same rocks the results of mathematical treatment is not consistent with the data (Tables 2, 6–9). This discrepancy corresponds to a desequilibrium between chlorite and phengite.These results imply a continuous metamorphic evolution between two stages (Fig. 6): a first stage (1) at 8 kb, 350 ° C; a second stage (2) at 2 to 3 kb, 400–450 ° C.     

Metamorphic evolution of medium‐temperature ultra‐high pressure (MT‐UHP) eclogites from the South Dabie orogen,Central China: an insight from phase equilibria modelling

Medium‐temperature ultrahigh pressure (MT‐UHP) eclogites from the south Dabie orogen, as represented by samples from the Jinheqiao, Shuanghe and Bixiling areas, consist of garnet, omphacite, phengite, epidote, hornblendic amphibole, quartz/coesite and rutile with or without kyanite and talc. Garnet is mostly anhedral and unzoned, but a few porphyroblasts are weakly zoned with core–mantle increasing grossular (X_gr) and decreasing pyrope (X_py) contents. Garnet compositions are closely correlated with the bulk compositions. For instance, the X_py and X_gr contents are positively correlated with the bulk MgO and CaO contents. Phengite is occasionally zoned with core–rim deceasing Si content, and phengite grains as inclusions in garnet show higher Si than in the matrix, suggesting differently resetting during post‐peak stages. The maximum Si contents are mostly 3.60–3.63 p.f.u. for the three areas. Pseudosections calculated using THERMOCALC suggest that the MT‐UHP eclogites should have a peak assemblage of garnet + omphacite + lawsonite + phengite + coesite in most rocks of higher MgO content. In this assemblage, the X_py in garnet mostly depends on bulk compositions, whereas the X_gr in garnet and the Si contents in phengite regularly increase, respectively, as temperature and as pressure rise, and thus, can provide robust thermobarometric constraints. Using the X_gr and Si isopleths in pseudosections, the peak P–T conditions were estimated to be 40 kbar/730 °C for the Jinheqiao, 41 kbar/726 °C for the Shuanghe, and 37–52 kbar and 700–830 °C for the Bixiling eclogites. Some eclogites with higher FeO are predicted to have a peak assemblage of garnet + omphacite + coesite ± phengite without lawsonite, where the garnet and phengite compositions highly depend on bulk compositions and generally cannot give available thermobarometric constraints. Decompression of the eclogites with lawsonite in the peak stage is inferred to be accompanied with cooling and involves two stages: an early‐stage decompression is dominated by lawsonite dehydration, resulting in increase in the mode of anhydrous minerals, or further eclogitization, and formation of epidote porphyroblasts and kyanite‐bearing quartz veins in eclogite. As lawsonite dehydration can facilitate evolution of assemblages under fluid‐present conditions, it is difficult to recover real peak P–T conditions for UHP eclogites with lawsonite. This may be a reason why the P–T conditions estimated for eclogites using thermobarometers are mostly lower than those estimated for the coherent ultramafic rocks, and lower than those suggested from the inclusion assemblages in zircon from marble. A late‐stage decompression is dominated by formation of hornblendic amphibole and plagioclase with fluid infiltration. The lawsonite‐absent MT‐UHP eclogites have only experienced a decompression metamorphism corresponding to the later stage and generally lack the epidote overprinting.     

Borosilicate- and phengite-bearing veins from the Grenville Province of Labrador: evidence for rapid uplift

Quartzo‐feldspathic veins emplaced within a migmatite terrane near Wilson Lake in the Grenville Province of central Labrador record a metamorphic event not evident in the host rocks. The discordant veins are undeformed and have undisturbed primary igneous/hydrothermal textures. Most of the veins contain euhedral kyanite, as well as aggregates of kyanite, K‐feldspar, phlogopite and minor dumortierite which are likely pseudomorphs after primary phengite. The reconstructed phengite compositions range from 3.1 to 3.2 Si per 11 oxygen formula unit. The pseudomorph assemblage is interpreted as the product of phengite + quartz melting under H₂O‐undersaturated conditions, which brackets P–T conditions of formation to about 9–16 kbar and 775–875 °C. A parallel vein that is likely of the same generation contains the borosilicate phases, dumortierite, prismatine and grandidierite, but no kyanite. The borosilicate assemblages constrain the P–T conditions of vein crystallization to ≥10 kbar and c. 750–850 °C. Vein emplacement is constrained to T ≤ 875 °C at the same pressures, which is well within the kyanite zone. Because the host rocks and veins must have experienced the same P–T history following vein emplacement, the presence of unreacted sillimanite in the host migmatites implies insufficient time for host rock equilibration. Slow reaction rates because of anhydrous conditions are not a likely explanation given the abundance of biotite and hornblende in the host rocks. The ductility implied by the breakdown of a hydrous phase (phengite) and the production of an H₂O‐undersaturated melt in the veins contrasts with the apparently brittle behaviour of the host rocks. The absence of deformation since the time of vein emplacement, even at temperatures above 750 °C, suggests that the deep crust in this part of Labrador had a very short residence time under conditions of the kyanite zone. Rapid decompression from those conditions is consistent with quartz + phengite melting and accounts for the relatively brittle behaviour of the terrane as it was uplifted.     

Partial melting of a phlogopite-clinopyroxenite nodule from south-west Uganda: an experimental study bearing on the origin of highly potassic continental rift volcanics

Melting experiments on a mantle-derived nodule assemblage consisting of clinopyroxene, phlogopite and minor titanomagnetite, sphene and apatite have been done at 20 and 30 kbar between 1,175 and 1,300° C. The nodule composition was selected on the basis of modal and chemical analyses of 84 mantle derived nodules with metasomatic textures from the Katwe-Kikorongo and Bunyaruguru volcanic fields of south-west Uganda. At 30 kbar, 1,225 and 1,250° C, representing 20–30% partial melting, the compositions of glasses compare favourably to those of the average composition of 26 high potassic mafic lavas from the same region. Glasses produced by sufficiently low degrees of partial melting at 20 kbar could not be analysed. Glass compositions obtained for 20–30% melting at 30 kbar have high K₂O (3.07–5.05 wt.%), low SiO₂ (35.0–39.2 wt.%), high K/K + Na (0.54–0.71), K + Na/Al (0.99–1.08) and Mg/ Mg + Fe_T of 0.59–0.62. These results support the suggestion of Lloyd and Bailey (1975) that the nodules represent the source material for the high K-rich lavas of south-west Uganda. If this conclusion is correct it implies that anomalous mantle source of phlogopite clinopyroxenite composition could produced the Ugandan lavas by relatively higher degrees of partial melting than that normally considered for highly alkaline mafic magmas derived from a pyrolitic mantle source. Higher degrees of melting are considered likely from such a different source region, rich in alkalis, water and radioactive elements. Steeper geotherms and increased fluxing of sub-rift mantle by degassing would also produce higher degrees of partial melting.     

A thermodynamic model for Fe–Mg dioctahedral K white micas using data from phase-equilibrium experiments and natural pelitic assemblages

The purpose of this study is to derive a solid-solution model for potassic white micas (KWM) encountered in rocks of various bulk compositions, over a wide range of P-T conditions. A compilation of phengite compositions lead us to propose a seven-thermodynamic-component (muscovite, Fe²⁺-Al-celadonite, Mg-Al-celadonite, annite, phlogopite, pyrophyllite and paragonite) ionic solid-solution model which accounts for the Tschermak, Fe-Mg, di/trioctahedral, pyrophyllitic and paragonitic substitutions observed in nature. A four-site mixing model with symmetric Margules parameters to model the Tschermak substitutions, asymmetric Margules parameters to model the other substitutions, and ideal intersite interaction has been adopted. In contrast to previous models, the relevant thermodynamic data and solid-solution properties are calibrated with independent sets of published experiments conducted for the KMASH, KFASH, KFMASH, and KNASH systems, as well as about 200 natural data involving KWM assemblages. The constraints span a wide range of pressure and temperature conditions (150 to 750 °C, 0.5 to 30 kbar), so that our model does not need to be extrapolated outside the calibration range to be used for P-T thermobarometric purposes. The calculated thermodynamic data are interconsistent with the TWQ thermodynamic database and solid-solution models, including that recently published for chlorites.     

Phase relations in high-pressure metapelites in the system KFMASH (K2O–FeO–MgO–Al2O3–SiO2–H2O) with application to natural rocks

Using a previously published, internally consistent thermodynamic dataset and updated models of activity–composition relations for solid solutions, petrogenetic grids in the model system KFMASH (K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O) and the subsystems KMASH and KFASH have been calculated with the software THERMOCALC 3.1 in the P–T range 5–36 kbar and 400–810 °C, involving garnet, chloritoid, biotite, carpholite, talc, chlorite, staurolite and kyanite/sillimanite with phengite, quartz/coesite and H₂O in excess. These grids, together with calculated AFM compatibility diagrams and pseudosections, are shown to be powerful tools for delineating the phase equilibria and P–T conditions of pelitic high-P assemblages for a variety of bulk compositions. The calculated equilibria and mineral compositions are in good agreement with petrological observation. The calculation indicates that the typical whiteschist assemblage kyanite–talc is restricted to the rocks with extremely high X_Mg values, decreasing X_Mg in a bulk composition favoring the stability of chloritoid and garnet. Also, the chloritoid–talc paragenesis is stable over 19–20 kbar in a temperature range of ca. 520–620 °C, being more petrologically important than the previously highlighted assemblage talc–phengite. Moreover, contours of the calculated Si isopleths in phengite in P–T and P–X pseudosections for different bulk compositions extend the experimentally derived phengite geobarometers to various KFMASH assemblages.     

The pyrope-coesite rocks and their country rocks at Parigi,Dora Maira Massif,Western Alps: detailed petrography,mineral chemistry and PT-path

Both the coarse- and fine-grained varieties of the partly coesite-bearing pyrope-quartzites, their interlayered jadeite-kyanite rocks, and the biotite-phengite gneiss country rock common to all of them were subjected to detailed petrographic and textural studies in order to determine the sequence of crystallisation of their mineral constituents, which were also studied analytically by microprobe. Prior to pyrope and coesite growth, the Mg-rich metapelites were talc-kyanite-chlorite-rutile-ellenbergerite schists which — upon continued prograde metamorphism — developed first pyrope megacrysts in silica-deficient local environments at the expense of chlorite + talc + kyanite, and subsequently the smaller pyrope crystals with coesite inclusions from reacting talc + kyanite. Based on geobarometrically useful mineral inclusions as well as on experimentally determined phase relations, a prograde PT-path — simplified for water activity = 1 — is constructed which passes through the approximate PT-conditions 16 kbar and 560° C, 29 kbar and 720° C, and finally up to 37 kbar at about 800° C, where the Mg-rich metapelite was a pyrope-coesite rock with phengite, kyanite, and talc still present. During the retrograde path, pyrope was altered metasomatically either into phlogopite + kyanite + quartz or, at a later stage, to chlorite + muscovite + quartz. Both assemblages yield PT-constraints, the latter about 7–9 kbar, 500–600° C. The country rock gneisses have also endured high-pressures of at least 15 kbar, but they provide mostly constraints on the lowest portion of the uplift conditions within the greenschist facies (about 5 kbar, 450° C). Microprobe data are presented for the following minerals: pyrope, ellenbergerite, dumortierite (unusually MgTi-rich), jadeite, vermiculite (formed after Na-phlogopite?), paragonite, and for several generations of phengite, chlorite, talc, phlogopite, dravite, and glaucophane in the high-pressure rocks, as well as for biotite, chlorite, phengites, epidote, garnet, albite, and K-feldspar in the country rock gneisses. An outstanding open problem identified in this study is the preservation of minerals as inclusions within kyanite and pyrope beyond their PT-stability limits.     

Metamorphism, geochemistry and origin of magnesian volcanic rocks, Klamath Mountains, California

Metabasaltic rocks in the Klamath Mountains of California with ‘komatiitic’ major element concentrations were investigated in order to elucidate the origin of the magnesian signature. Trace-element concentrations preserve relict igneous trends and suggest that the rocks are not komatitic basalts, but immature arc rocks and within-plate alkalic lavas. Correlation of ‘excess’ MgO with the volume per cent hornblende (±clinopyroxene) suggests that the presence of cumulus phases contributes to the MgO-rich compositions. Early submarine alteration produced regional δ¹⁸O values of +10±1.5%_° and shifts in Al₂O₃, Na₂O, and K₂O concentrations. Regional metamorphic grade in the study area varies from biotite-zone greenschist facies (350–550°C, c. 3 kbar) southward to prehnite–actinolite facies (200–400°C, ≤3 kbar), but little isotopic or elemental change occurred during the regional recrystallization. The greenschist facies assemblage is actinolitic hornblende + phengite + epidote + sodic plagioclase + microcline + chlorite + titanite + hematite + quartz in Ti-poor metabasaltic rocks; in addition to these phases biotite is present in Ti-rich analogues. Lower grade greenstones contain prehnite and more nearly stoichiometric actinolite. The moderate to low pressures of regional metamorphism are compatible with P–T conditions in a magmatic arc. Later contact metamorphism at 2–2.9±0.5 kbar and at peak temperatures approaching 600° C around the English Peak and Russian Peak granodiorites produced 3–4–km-wide aureoles typified by gradual, systematic increases in the pargasite content of amphibole, muscovite content of potassic white mica, and anorthite content of plagioclase compositions. Metasomatism during contact metamorphism produced further increases in bulk-rock δ¹⁸O_SMOW of as much as +6%_°. Thus, the unusually MgO-rich nature of the Sawyers Bar rocks may be attributed at least partly to metasomatism and the presence of magnesian cumulus phases.     

Vesuvianite-wollastonite-grossular-bearing calc-silicate rock near Tatapani,Surguja district,Chhattisgarh

This paper reports the occurrence of vesvianite + wollastonite + grossular + diopside + microcline + quartz assemblage in an enclave of calc-silicate rocks occurring within quartzofeldspathic gneiss near Tatapani in the western part of Chhotanagpur Gneissic Complex. The enclave contains phlogopite-absent and phlogopite-bearing calc-silicate rocks, the latter being much more abundant than the former. The above assemblage occurs in the phlogopite-absent rock. Phlogopite-bearing rock contains the assemblage phlogopite + salite + microcline + plagioclase + quartz. A strong schistosity is developed in both the calc-silicate rocks and the minerals are syntectonic with the major foliation-forming event in the area. The vesuvianite-bearing assemblage is formed by amphibolite facies regional metamorphism of a calcareous protolith at pressure < 4 kbar and X_{CO 2} (fluid) < 0.15.     

On the origin of some mica-lamprophyres: experimental evidence from a mafic minette

Experimental melting relationships for a mafic minette (mica-lamprophyre) from Buell Park, Arizona were determined under fO₂ conditions equivalent to the ironwüstite-graphite and quartz-fayalite-magnetite buffers, at pressures of 10–20 kbar. A comparison between experimental products and phenocrysts in the most primitive minettes indicates that those lavas preserve a near-liquidus assemblage of olivine, diopside and Ti-rich phlogopite crystallized in the upper mantle under fO₂QFM and in the presence of an H₂O-bearing fluid phase. It is suggested that micalamprophyric (minette) magmas may originate from a metasomatized, garnet-bearing peridotitic source at deeper levels in the mantle (P20 kbar) but can also be in equilibrium with a phlogopite-bearing wehrlite (±opx) source at pressures of 17–20 kbar, under reducing or oxidizing mantle conditions. Owing to their rapid crystallization rate and high liquidus temperatures, a series of potassic daughter melts (potassic latites and felsic minettes) can be formed by segregation from mafic minette parents during their ascent through the cooler continental crust. The preservation of olivine in equilibrium with phlogopite phenocrysts in primitive minettes precludes a petrogenetic process dominated by assimilation/fractional crystallization in a shallow magma chamber and supports a model by which some lamprophyric magmas are brought to near surface conditions at temperatures in the range of 1,000–1,200° C and chilled rapidly.     

Mineralogy of New Caledonian metamorphic rocks

Variations in chemistry and related physical properties of sheet silicates in the Ouégoa district with metamorphic grade are investigated. Weakly metamorphosed rocks prior to the crystallization of lawsonite contain phengite (d ₀₀₆=3.317–3.323 Å), chlorite and occasionally paragonite while interstratified basaltic sills contain chlorite, minor phengite and stilpnomelane. Pyrophyllite crystallizes before lawsonite in some metamorphosed acid tuffs and is also stable in the lawsonite zone. Paragonite, phengite and chlorite appear to be stable through the sequence from weakly metamorphosed rocks into high-grade “eclogitic” schists and gneisses. Optical, chemical and some X-ray diffraction data is given for representative sheet silicates. Electron probe analyses of 55 phengites, 21 paragonites, 57 chlorites, 12 vermiculites, 2 stilpnomelanes, and 2 chloritoids are presented in graphical form. All K-micas analysed are consistently phengitic (3.29–3.55 Si^iv ions per formula unit) and show limited solid solution with paragonite (4 to 13% Pa). The K∶Na ratio of the phengite is strongly dependant on the assemblage in which it occurs; the amount of phengite component and its Fe∶Mg ratio depends on bulk-rock composition. Phengites from acid volcanics have the highest Fe∶Mg ratio, highest phengite component and β refractive indices. Phengites from basic volcanics and metasediments of the epidote zone have the lowest Fe∶Mg ratio. Phengites from lawsonite-zone metasediments have intermediate Fe∶Mg ratios. The phengites show a small decrease in phengite component with increasing metamorphic grade. d ₀₀₆ for phengites varied from 3.302 to 3.323 Å but at least in the lawsonite and epidote zones appears to reflect composition and had little systematic variation with metamorphic grade; phengites from very low-grade rocks showed the longest values of d ₀₀₆. Paragonite shows almost no phengite-type substitution and only limited solid solution (4–12%) with muscovite. All paragonites (6) and most phengites (20) which have been examined are 2M₁ polymorphs; one Fe²⁺-phengite appears to be a 1M polymorph. The chemistry of chlorites closely reflects parent-rock chemistry. Chlorites from metasediments have distinctly higher Fe/(Fe+Mg) ratios than chlorites from basic igneous rocks; chlorites from the lawsonite and lawsonite-epidote transitional zone metasediments have the highest Fe/(Fe+Mg) ratios. In metabasalts Fe/(Fe+Mg) ratios appear to reflect individual variations in bulk-rock chemistry and show no direct correlation with metamorphic grade. There is little difference in Al/(Si+Al) ratio between chlorites from sediments and basic igneous rocks although in both lithologies the chlorites from the epidote zone appear to be slightly more aluminous. Fe-rich chlorites of the lawsonite zone metasediments have been altered by a process involving leaching of Fe and Mg and introduction of alkalies to a brown pleochroic Fe-vermiculite. Chemical and physical data for this vermiculite are given. The decrease in Fe/(Fe+Mg) ratio in chlorites and phengites on passing from the lawsonite to the epidote zone can be correlated with the crystallization of Fe-rich epidote and almandine in the epidote zone. Elemental partitioning between coexisting minerals has shown Ti to be partitioned into phengite, while Fe and Mn are strongly partitioned into chlorite. When either stilpnomelane or chloritoid coexists with phengite or chlorite, Fe and Mn are slightly enriched in the stilpnomelane or chloritoid relative to the chlorite.     

Phlogopite-biotite parageneses from the K-mafic-carbonatite effusive magmatic association of Katwe-Kikorongo, SW Uganda

Summary Ti-bearing phlogopite-biotite is dominant in Ugandan kamafugite-carbonatite effusives and their entrained alkali clinopyroxenite xenoliths. It occurs as xeno/phenocrysts, microphenocrysts and groundmass minerals and also as a major xenolith mineral. Xenocrystic micas in kamafugites and carbonatites are aluminous (> 12 wt% Al₂O₃), typically contain significant levels of Cr (up to 1.1 wt% Cr₂O₃), and are Ba-poor. Microphenocryst and groundmass micas in feldspathoidal rocks extend to Al-poor compositions, are depleted in Cr, and are generally enriched in Ba. In general, xenocrystic micas occupy the Al₂O₃ and TiO₂ compositional field of the xenolith mica, and on the basis of Mg#, and high P, T experimental evidence they probably crystallised at mantle pressures. Mica xenocryst Cr contents range from those in Cr-poor megacryst and MARID phlogopite to higher values found in primary and metasomatic phlogopites in kimberlite-hosted peridotite xenoliths. Such Cr contents in Ugandan mica xenocrysts are considered consistent with derivation from carbonate-bearing phlogopite wehrlite and phlogopite-clinopyroxenite mantle. Olivine melilitite xenocryst micas are distinguished by higher Mg# and Cr content than mica in clinopyroxenite xenoliths and mica in Katwe-Kikorongo mixed melilitite-carbonatite tephra. Higher Al₂O₃ distinguishes Fort Portal carbonatite xenocrysts and some contain high Cr. It is suggested that the genesis of Katwe-Kikorongo olivine melilitite and Fort Portal carbonatite involves a carbonate-bearing phlogopite wehrlite source while the source of the mixed carbonatite-melilitite rocks may be carbonate-bearing phlogopite clinopyroxenite. Received January 24, 2000; revised version accepted September 27, 2001