Local and regional differences in the chemical potential of water in amphibolite facies pelitic schists

Abstract Mineral assemblages in different samples of amphibolite facies pelitic schists collected from two separate outcrops in the Moosilauke area, NH, record differences in the chemical potential of water during metamorphism. Mineralogical, petrological, and field relations indicate that mineral assemblages at both outcrops equilibrated at 520°C and 3.5–4.0 kbar. Thermodynamic analysis of the mineral assemblages demonstrates that maximum chemical potential differences at each outcrop were of the order of 150 calories, over distances of 10–20 m.
The differences in the chemical potential of water recorded in both bed-to-bed and outcrop-to-outcrop relations are consistent with the following conclusions: (1) mineral assemblages on a specific outcrop did not equilibrate with an external reservoir of fluid of fixed composition, (2) the relatively small magnitude of the chemical potential differences suggests little or no infiltration of externally derived fluid, (3) these differences on the outcrop scale are probably related to initial compositional variations and the buffer capacity of the mineral assemblage, and (4) the different values of the chemical potential of water exhibited by the various mineral assemblages permits an understanding of the effects of variable μ_H2O for amphibolite facies pelitic schists.     

Evidence from mineral assemblages for infiltration of pelitic schists by aqueous fluids during metamorphism

Prograde mineral assemblages and compositions have been predicted for pelitic schist in the 10 component system Na₂O–K₂O–CaO–MnO–FeO–MgO–Al₂O₃–SiO₂–CO₂–H₂O for three cases of prograde metamorphism and fluid-rock interaction: (1) increasing temperature (T) at constant pressure (P) and constant pore fluid volume (1%) without infiltration (no-infiltration case); (2) increasing T at constant P accompanied by sufficient fluid infiltration that fluid composition is at all times constant (large-flux case); and (3) increasing T at constantP accompanied by a timeintegrated fluid flux f 10⁴ cm^{3 cm 2} (intermediate-flux case). Stable mineral assemblages and compositions were calculated by solving a system of non-linear equations that specify mass balance and chemical equilibrium between minerals and fluid. The model pelitic system includes quartz, muscovite, plagioclasc, chlorite, ankerite, siderite, biotite, garnet, staurolite, andalusite, kyanite, sillimanite, K-feldspar, and a coexisting, binary H₂O–CO₂ fluid. Specifically, prograde thermal metamorphism was modelled for Shaw's (1956) average low-grade pelite and for a moderate range of bulk rock compositions at P=3, 5, and 7 kb and initial fluids with Xco ₂ ^o =0.02–0.40. The model predicts a carbonate-bearing mineral assemblage for average pelite under chlorite zone conditions composed of quartz, muscovite, albite, chlorite, ankerite, and siderite. The mineral assemblages predicted for the noinfiltration case are unlike those typically observed in regional metamorphic terranes. Simulations of metamorphism for the large-flux and intermediate-flux cases, however, reproduce the sequence of mineral assemblages observed in normal Barrovian regional metamorphic terranes. These results suggest that regional metamorphism of pelitic schists is typically associated with infiltration of significant quantities of aqueous fluid.     

A model for garnet and plagioclase growth in pelitic schists: implications for thermobarometry and P-T path determinations

Numerical models of the progressive evolution of pelitic schists in the NCMnKFMASH system with the assemblage garnet + biotite + chlorite ± staurolite + plagioclase + muscovite + quartz + H₂O are presented with the goal of predicting compositional changes in garnet and plagioclase along different P-T paths. The numerical models support several conclusions that should prove useful for interpreting the P-T paths of natural parageneses: (i) Garnet may grow along P-T vectors ranging from heating with decompression to cooling with compression. P-T paths deduced from garnet zoning that are inconsistent with these growth vectors are self-contradictory. (ii) There is a systematic relation between garnet and plagioclase composition and growth such that for most P-T paths, garnet growth requires plagioclase consumption. Furthermore, mass balance in a closed system requires that as plagioclase is consumed the remaining plagioclase becomes increasingly albitic. Inclusions of plagioclase in the core of garnet should be more anorthitic than those near the rim and zoned matrix plagioclase should have rims that are more albitic than the cores. Complex plagioclase textures may arise from the local variability of growth and precipitation kinetics. (iii) A decrease of Fe/(Fe + Mg) in a garnet zoning profile is a reliable indicator of increasing temperature for the assemblage modelled. However, there is no single reliable ΔP monitor and inferences about ΔP can only be made by considering plagioclase and garnet together. (iv) Consumption of garnet during the production of staurolite removes material from the outer shell of a garnet and may make recovery of peak metamorphic compositions and P-T conditions impossible. Low ‘peak’temperatures typically recorded by staurolite-bearing assemblages may reflect this phenomenon. (v) Diffusional homogenization of garnet affects the computed P-T path and results in a clockwise rotation of the computed P-T vector relative to the true P-T path.     

Monazite U-Pb dating of staurolite grade metamorphism in pelitic schists

A study of the occurrence of and relations between rare-earth element (REE) minerals in pelitic schists indicates that monazite forms at or near the P and T of the staurolite isograd. Samples at staurolite grade from the Silurian Perry Mountain Formation in the Rumford quadrangle of Maine yield monazite in sufficient quantities to permit accurate dating of the metamorphic events forming the monazites. The bulk chemistry of the metapelites, as seen in the major element abundances and REE patterns, does not vary significantly across the study area. Thus the appearance and disappearance of REE phases is assumed to reflect changes in metamorphic grade. In a sample from the biotite zone, scanning electron microscope and microprobe studies show allanite and monazite intimately associated on a 10 m scale. The texture suggest that metastable detrital monazite breaks down, distributing its REE components to allanite. From samples below staurolite grade in which monazite is not present, our observations suggest that REEs are partitioned into allanite. At or near the staurolite isograd monazite forms as a metamorphic mineral, initiating its role as a geochronometer. Garnet-biotite geothermometry on samples at this grade from this and other studies places constraints on the minimum temperature necessary to form monazite: 525° C±25°C at 3.1±0.25 kbar. A total of 15 separates from nine schist samples ranging up to sillimanite grade have been dated. Each date is remarkably concordant, even though petrologic and textural studies by previous workers have shown that the rocks in the area have been affected by at least three metamorphic episodes. Calculations indicate insignificant Th disequilibrium in these monazites. The conditions associated with the metamorphic events suggest that monazite remains closed to lead loss provided that subsequent metamorphisms are at or below sillimanite grade. Two distinct metamorphic events are resolved, one at around 400 Ma and one at about 370 Ma. The latter was due to thermal effects of a nearby pluton that yields concordant monazite ages of 363 Ma. This work suggests that in addition to dating plutonism and high-grade metamorphism, monazite should be viewed as a reliable geochronometer for moderate metamorphism of pelitic schists.     

A petrogenetic grid for pelitic schists in the system SiO2-Al2O3-FeO-MgO-K2O-H2O

A quantitative petrogenetic grid for pelitic schists in the system KFMASH that includes the phases garnet, chlorite, biotite, chloritoid, cordierite, staurolite, talc, kyanite, andalusite, sillimanite, and pyrophyllite (with quartz, H₂O and muscovite or K-feldspar in excess) is presented. The grid is based on thermodynamic data of Berman et al. (1985) and Berman (1988) for endmember KFASH and KMASH equilibria and natural Fe-Mg partitioning for the KFMASH system. Calculation of P-T slopes and the change in Fe/(Fe+Mg) along reactions in the KFMASH system were made using the Gibbs method. In addition, the effect on the grid of MnO and CaO is evaluated quantitatively. The resulting grid is consistent with typical Buchan and Barrovian parageneses at medium to high grades. At low grades, the grid predicts an extensive stability field for the paragenesis chloritoid+biotite which arises because of the unusual facing of the reaction chloritoid+biotite + quartz+H₂O = garnet+chlorite+muscovite, which proceeds to the right with increasing T in the KFMASH system. However, the reaction proceeds to the left with increasing T in the MnKFASH system so the assemblage chloritoid + biotite is restricted to bulk compositions with high Fe/(Fe+Mg+Mn). Typical metapelites will therefore contain garnet+chlorite at low grades rather than chloritoid + biotite.     

Rare earth elements in Silurian pelitic schists from N.W. Maine

Thirty-two samples of a series of metamorphosed Silurian (?) pelitic schists in the greenschist and amphibolite facies from N.W. Maine have been analyzed for their rare-earth element (REE) content. The REE contents of these samples do not change as a function of metamorphic grade. Two different metasedimentary formations have been sampled, and they differ significantly in their light REE content. The absolute and relative distribution of the REE in the Bangeley Formation are quite similar to the composites of N. American, European and Russian shales that have been determined thus far (e.g. median La/Lu ratio of the Bangeley Formation normalized to chondrites = 8.7 ± 3.0). Samples from the Perry Mt. Formation show large depletions in the light REE compared to the Bangeley Formation and previously analyzed shale and metamorphosed shale samples, but heavy REE concentrations that are quite similar to the other samples (e.g. median La/Lu ratio of the Perry Mt. normalized to chondrites = 1.2 ± 0.6). These differences in light REE content between the Perry Mt. Formation and other sedimentary rocks are probably due to differences in the original clay mineral compositions as modified by weathering and/or depositional environments.     

Textural relations in melanosomes of selected specimens of migmatitic pelitic schists: Implications for leucosome-generating processes

Melanosome textures in several specimens of migmatitic pelitic schists are evaluated to test leucosome-generating reactions inferred independently on the basis of mineralogic and chemical relationships in the melanosomes. Systematic variations in grain numbers per unit volume, grain sizes, size distributions, and shapes, and grain contact frequencies within melanosomes can be attributed to leucosome generation. These variations support independent inferences of reactions based on modes and chemistry and, in one case, suggest a refinement of reactions inferred on these bases.In these specimens, at least, textures resulting from the leucosome-generating process have not been obliterated by later recrystallization and provide information regarding this process. These textures indicate that leucosome generation involved preferential reaction at mice-quartz and feldspar-quartz grain boundaries. This conclusion is in agreement with melting processes observed in short-term melting experiments.     

Alpine metamorphism of pelitic schists in the Nufenen Pass area, Lepontine Alps

Abstract The effects of Tertiary Alpine metamorphism on pelitic Mesozoic cover rocks have been studied along a cross-section in the central Lepontine Alps in the Nufenen Pass area, Switzerland. Greenschist facies to amphibolite facies conditions are indicated by the formation of the index minerals chloritoid, garnet, staurolite and kyanite in pelitic rocks. Regional metamorphism reached maximum conditions during the interkinematic period between a main Alpine penetrative (D2) and a late Alpine (D3) crenulation type deformation phase or synchronous with the late Alpine deformation. Based on AFM phase relationships four different metamorphic zones can be distinguished: (1) chloritoid zone; (2) staurolite + chlorite zone; (3) staurolite + biotite zone; and, (4) kyanite zone. The isograds that separate these zones can be modelled by univariant reactions in the KFMASH system. The conditions of metamorphism calculated from geological ther-mobarometers for the maximum post-D2 por-phyroblast stage are from North to South: 500° C at 5-6 kbar and 600° C at 7-8 kbar. Detailed thermobarometry of garnet por-phyroblasts with complex textures suggests that maximum temperature was reached later than maximum pressure. Early garnet growth occurred along a prograde P-T-path, post-D2 rims grew with increasing temperature but decreasing pressure, and finally post-D3 garnet formed along a retrograde P-T-path. It may be concluded from the calculated pressure and temperature difference over a short distance (3 km) across the mapped area that the isogradic surfaces of the post-D2 metamorphism are steeply oriented. The data also suggest that isobaric and isothermal surfaces are parallel. Much of the observed metamorphic pattern can be explained as the result of a significant post-D2 differential uplift of the hot Pennine area relative to the Helvetic area along a tectonic contact zone. The closely spaced isograds (isotherms) in the North may then be interpreted as a thermal effect owing to the emplacement of the hot Pennine rocks against the Got-thard massif with its cover. Whereas, in the Pennine metasediments, post-D2 porphyroblast formation can be related to the decompression path which was steep enough for dehydration reactions to proceed. It is also remarkable that late kyanite porphyroblasts probably formed with decreasing pressure. The interpretation given here for the Nufenen Pass area may also apply to the Luk-manier Pass area where similar metamorphic patterns have been reported by Fox (1975). The formation of the ‘Northern Steep Belt’;, as denned by Milnes (1974b), and the associated late Alpine fold zones may, therefore, have significantly modified the metamorphic pattern of the Helvetic-Penninic contact zone.     

A Comparative geochemical study of pelitic schists and metamorphosed carbonate rocks from south-central Maine,USA

Whole-rock major element chemical analyses of progressively metamorphosed impure carbonate rocks and pelitic schists, collected from the same metamorphic terrain, reveal similarities and differences in the chemical response of these rock types to the metamorphic event. Relative to a constant aluminum reference frame, both schist and carbonate exhibit no detectable change in their contents of Fe, Mg, Ti, Si, and Ca with change in metamorphic grade. Carbonate rocks become progressively depleted in K and Na with increasing grade of metamorphism, while schists exhibit no statistically significant change in their contents of K and Na. Both rock types become depleted in volatiles (principally CO₂ and H₂O) with increasing grade.Whole-rock chemical data permit two mechanisms for migration of K and Na from the carbonate rocks during metamorphism: (a) diffusion of alkalis from carbonate to adjacent schist; (b) transport of alkalis by through-flowing metamorphic fluid (infiltration). Mineral equilibria in schist and metacarbonate rock from the same outcrops allow calculation of the affinity for cation exchange between the two rock types during metamorphism. Measured affinities indicate that if mass transport of K and Na occurred by diffusion, chemical potential gradients would have driven the alkalis from schist into carbonate rock. Because diffusion cannot produce the observed chemical trends in the metacarbonates, K and Na are believed to have been removed during metamorphism by infiltration.The disparity in chemical behavior between the pelitic schists and metacarbonate rocks may be a result of enhanced fluid flow through the carbonates. The carbonate rocks may have acted as metamorphic aquifers; the greater flow of fluid through them would then have had a correspondingly greater effect on their whole-rock chemistry.     

Carbonaceous material in pelitic schists of the Sanbagawa metamorphic belt in central Shikoku,Japan

Carbonaceous material in pelitic schists of the Sanbagawa metamorphic belt in central Shikoku, Japan, was separated from the host rocks and its X-ray diffraction and chemical composition were studied. Its crystal structure and chemistry change continously with increasing metamorphic grade and approach those of well-ordered graphite near the biotite isograd. As graphitization is a rate process, the temperature of complete graphitization differs from one metamorphic terrain to another as a function of the duration of metamorphism. In an individual metamorphic terraan, however, the degree of graphitization is a useful indicator of relative metamorphic temperature in lower-grade rocks.     

Morphology of intergranular pores and wetting angles in pelitic schists studied by transmission electron microscopy

In pelitic schists composed mainly of quartz and albite grains, the morphology of intergranular pores, which were filled with water, was studied by transmission electron microscopy (TEM). Although some pores are defined by crystallographic planes (F-face), most of their form has an ideal shape determined by interface tensions between grains and fluid. High-resolution TEM observations demonstrate that pore-free regions at grain boundaries are tight even at the nanometer scale, showing that the wetting angle is larger than 0° in this rock. The pore distribution in two-grain junctions can be compared to a "necklace microstructure" developed by instability of a fluid film along the boundary induced by microcracking. Wetting angles for pores located at grain edges of quartz and albite decrease in the order albite/albite, quartz/quartz, and quartz/albite. The quartz/quartz wetting angle in a calcite-free sample is smaller than that in a calcite-containing sample. This angle also changes due to grain misorientation. Our results confirm that solid-solid and solid-fluid interfacial energies control the geometry of intergranular fluid in natural rocks.     

Bulk chemical control on metamorphic monazite growth in pelitic schists and implications for U–Pb age data

Several petrographic studies have linked accessory monazite growth in pelitic schist to metamorphic reactions involving major rock‐forming minerals, but little attention has been paid to the control that bulk composition might have on these reactions. In this study we use chemographic projections and pseudosections to argue that discrepant monazite ages from the Mount Barren Group of the Albany–Fraser Orogen, Western Australia, reflect differing bulk compositions. A new Sensitive High‐mass Resolution Ion Microprobe (SHRIMP) U–Pb monazite age of 1027 ± 8 Ma for pelitic schist from the Mount Barren Group contrasts markedly with previously published SHRIMP U–Pb monazite and xenotime ages of c. 1200 Ma for the same area. All dated samples experienced identical metamorphic conditions, but preserve different mineral assemblages due to variable bulk composition. Monazite grains dated at c. 1200 Ma are from relatively magnesian rocks dominated by biotite, kyanite and/or staurolite, whilst c. 1027 Ma grains are from a ferroan rock dominated by garnet and staurolite. The latter monazite population is likely to have grown when staurolite was produced at the expense of garnet and chlorite, but this reaction was not intersected by more magnesian compositions, which are instead dominated by monazite that grew during an earlier, greenschist facies metamorphic event. These results imply that monazite ages from pelitic schist can vary depending on the bulk composition of the host rock. Samples containing both garnet and staurolite are the most likely to yield monazite ages that approximate the timing of peak metamorphism in amphibolite facies terranes. Samples too magnesian to ever grow garnet, or too iron‐rich to undergo garnet breakdown, are likely to yield older monazite, and the age difference can be significant in terranes with a polymetamorphic history.     

Polymetamorphic evolution of pelitic schists and evidence for Permian low-pressure metamorphism in the Vepor Unit, West Carpathians

Phase equilibrium modelling and monazite microprobe dating were used to characterize the polymetamorphic evolution of metapelites from the northern part of the Vepor Unit, West Carpathians. Three generations of garnet and associated metamorphic assemblages found in these rocks correspond to three distinct metamorphic events related to the Variscan orogeny, a Permian phase of crustal extension and the Alpine orogeny. Variscan staurolite‐bearing and Alpine chloritoid‐bearing assemblages record medium‐temperature and medium‐pressure regional metamorphisms reaching 540–570 °C/5–7.5 kbar and 530–550 °C/5–6.5 kbar respectively. The Permian metamorphic assemblage involves garnet, andalusite, sillimanite, biotite, muscovite, plagioclase and corundum and locally forms silica‐undersaturated andalusite‐biotite‐spinel coronas around older staurolite. The transition from andalusite to sillimanite indicates a prograde low‐pressure and medium‐temperature metamorphism characterized by temperature increase from 500 to 650 °C at ～3 kbar. As accessory monazite is abundant in the rocks, an attempt was made to derive its age of formation by means of electron microprobe‐based Th‐U‐Pb chemical dating. Despite the polymetamorphic nature of the metapelites, the monazite yielded uniform Permian ages. Microstructures confirm that monazite was formed in relation to the low‐pressure and medium‐temperature paragenesis, and the weighted average ages obtained for two different samples are 278 ± 5 and 275 ± 12 Ma respectively. The virtual lack of Variscan and Alpine monazite populations points to interesting aspects concerning the growth systematics of monazite in metamorphic rocks.     

High-pressure metamorphism in gneisses and pelitic schists in the East Rhodope zone (N. Greece)

Summary The high-alumina metapelites and the orthogneisses of the lower tectonic unit of East Rhodope underwent high P/T metamorphism followed by partial reequilibration during decompression under epidote-amphibolite/amphibolite facies to greenschist facies conditions. The high P/T mineral paragenesis in the orthogneisses is: quartz + albite + microcline + phengite (Si_max = 7 atoms p.f.u.) + biotite and in the high alumina metapelites: garnet + chloritoid + chlorite + phengite (Si_max. = 6.85 atoms p.f u.) + paragonite + quartz. Pressures between 14 and 15.5 kbar, for T_min = 550°C, are estimated for the high P/T metamorphism. During continuing uplift, staurolite + chlorite, staurolite + biotite and finally andalusite + Fe-ripidolite are grown at the expense of chloritoid in metapelites, while in the orthogneisses oligoclase, still coexisting with albite, is formed; in both rock types the Si content of white K-mica decreases considerably from almost pure phengite to pure muscovite.

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Hochdruck-Metamorphose in Gneisen und pelitischen Schiefern der östlichen RhodopeZone, Nord-Griechenland

Zusammenfassung Die Aluminium-reichen Metapelite und die Orthogneise der unteren tektonischen Einheit der östlichen Rhodope-Zone wurde unter hohen Drucken und Temperaturen metamorphosiert. Darauf folgte eine teilweise Reequilibration unter Druck-Entlastung bei Bedingungen der Epidot-Amphibolit/Amphibolit bis Grünschiefer Fazies. Die Hoch-P/T Mineral-Assoziation in den Orthogneisen besteht aus: Quarz + Albit + Mikroklin + Phengit (Si_max = 7 atoms p.f.u.) + Biotit und in den Aluminium-reichen Metapeliten: Granat + Chloritoid + Chlorit + Phengit (Si_max = 6.85 atoms p.f.u.) + Paragonit + Quarz. Drucke zwischen 14 and 15.5 kbar für T_min = 550°C wurden für die Hoch- P/T Metamorphose berechnet. Während andauernder Anhebung bildeten sich Staurolit + Chlorit, Staurolit + Biotit und schließlich Andalusit + Fe-Ripidolit auf Kosten von Chloritoid in den Metapeliten, während in den Orthogneisen Oligoklas der noch mit Albit koexistiert, gebildet wurde; in beiden Gesteinstypen nimmt der Si-Gehalt heller Kaliglimmer von fast reinem Phengit bis zu reinem Muskowit ab.

     

Step-wise growth of biotite porphyroblasts in pelitic schists of the western Lys-Caillaouas massif (Pyrenees)

Detailed optical and electron microscope (SEM and TEM) examination of biotite blasts from pelitic schists of the western Lys-Caillaouas massif in the Pyrenees reveals a variety of microstructures suggesting growth of the blasts before and after a thermal peak during the D₂ deformation. In the early stages of growth the biotites had (001) at high angles to S₁, and they appear to have existed as thin (001) parallel plates. In many cases blastesis is suggested to have involved growth of the biotites into their own continuously dilating pressure shadows. Inclusions with dentate grain boundaries, banded structures, and ‘radiator-fin’ intergrowths suggest a mechanism analogous to the Ramsay crack seal model for vein formation, but here involving step-wise dilation of a pressure-shadow cavity into which the adjacent blast itself was growing.     

Occurrence of lawsonite in pelitic schists from the Sanbagawa metamorphic belt, central Shikoku, Japan

The occurrence of lawsonite is described from pelitic schists of the lower-grade part of the pumpellyite-bearing subzone of the chlorite zone in the Asemi River area of central Shikoku. The lawsonite-bearing parageneses are consistent with the generally accepted view that the Sanbagawa facies series represents higher pressures than the lawsonite-bearing facies series in New Zealand.     

Metamorphic P-T paths from calcic pelitic schists from the Strafford Dome, Vermont, USA

Metamorphism of the Gile Mountain Formation and Waits River Formation in the Strafford Dome and Townshend-Brownington Syncline in east-central Vermont records two nappe-style events, D1 and D2, followed by doming. D1 formed a muscovite + biotite ± ilmenite schistosity subparallel to compositional layering, SO, and was followed by heating to garnet grade. The temperature and pressure at the end of D1 are estimated to be c . 450 C and 6-8 kbar. D2 variably crenulated and folded S1 during a nearly isothermal pressure increase of 1-2 kbar, calculated from compositions of garnet, which have inclusions trails with progressive crenulation and rotation of the S1 fabric. Similar P-T paths are computed for most of the area, suggesting that the later schistosity developed during emplacement of a regional nappe 3-6 km thick. There is a general lack of D3 (dome-stage) microstructures.
Near the Strafford-Willoughby Arch, staurolite and kyanite overgrew S2 in pelites, and plagioclase with increasing X _An overgrew S2 in calcic pelites, reflecting post-D2 heating to a maximum of 550-600 C. Metamorphic pressures at the end of D2 are fairly constant on the west side of the dome, indicating minor dome-stage uplift. In contrast, pressures at the thermal peak of metamorphism decrease by more than 4 kbar east of the dome. The observed pattern of isotherms and isobars is mainly the result of post-metamorphic, differential uplift and unroofing.
Finally, a minor, retrograde metamorphism produced the assemblage albite + epidote + K-feldspar + muscovite + chlorite, with grade increasing east toward the Connecticut River.     

The effect of whole-rock MnO content on the stability of garnet in pelitic schists during metamorphism

Garnet-bearing mineral assemblages are commonly observed in pelitic schists regionally metamorphosed to upper greenschist and amphibolite facies conditions. Modelling of thermodynamic data for minerals in the system Na₂O–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O, however, predicts that garnet should be observed only in rocks of a narrow range of very high Fe/Mg bulk compositions. Traditionally, the nearly ubiquitous presence of garnet in medium- to high-grade pelitic schists is attributed qualitatively to the stabilizing effect of MnO, based on the observed strong partitioning of MnO into garnet relative to other minerals. In order to quantify the dependence of garnet stability on whole-rock MnO content, we have calculated mineral stabilities for pelitic rocks in the system MnO–Na₂O–K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O for a moderate range of MnO contents from a set of non-linear equations that specify mass balance and chemical equilibrium among minerals and fluid. The model pelitic system includes quartz, muscovite. albite, pyrophyllite, chlorite, chloritoid, biotite, garnet, staurolite, cordierite, andalusite, kyanite. sillimanite, K-feldspar and H₂O fluid. In the MnO-free system, garnet is restricted to high Fe/Mg bulk compositions, and commonly observed mineral assemblages such as garnet–chlorite and garnet–kyanite are not predicted at any pressure and temperature. In bulk compositions with X_Mn= Mn/(Fe + Mg + Mn) > 0.01, however, the predicted garnet-bearing mineral assemblages are the same as the sequence of prograde mineral assemblages typically observed in regional metamorphic terranes. Temperatures predicted for the first appearance of garnet in model pelitic schist are also strongly dependent on whole-rock MnO content. The small MnO contents of normal pelitic schists (X_Mn= 0.01–0.04) are both sufficient and necessary to account for the observed stability of garnet.     

A model for phase equilibria in the prehnite-pumpellyite facies

Using the method of Schreinemakers, along with other thermodynamic considerations, a phase diagram for the system CaO-MgO-Al₂O₃-SiO₂-CO₂-H₂O was constructed. The phases prehnite, pumpellyite, calcite, chlorite, dolomite, quartz, tremolite, talc, zoisite, grossularite and vapor were considered in this construction. The results indicate that prehnite-pumpellyite facies mineral assemblages will only exist in equilibrium with a vapor phase in which the mole fraction of CO₂ is less than 0.2 at 1 kb, and less than 0.15 at 2 kb. Although talc could theoretically be a stable phase under these conditions, its common absence from rocks of this facies probably results from the existence of an enantiomorphic point which makes tremolite-calcite-CO₂ the stable assemblage at low X _{CO 2}, and the compositionally equivalent talc-calcite-CO₂ assemblage stable at moderate X _{CO 2}.