Petrology of Fe-Mg-carpholite-bearing metasediments from NE Oman

Abstract Fe-Mg carpholite occurs in metasediments of tectonically disrupted basement, shelf and foreland basin units that structurally underlie the Semail ophiolite in NE Oman. In the lower grade, structurally higher units, Fe-rich carpholite coexists with paragonite, quartz, illite, kaolinite and chlorite, whereas in deeper units, Fe-Mg carpholite occurs with pyrophyllite, sudoite, phengite and/or chloritoid. Mineral compositions in these units indicate that chlorite is more magnesian than coexisting Fe-Mg carpholite at low temperatures and pressures but, at higher metamorphic grades, X_Mg decreases in the order sudoite > carpholite > chlorite > chloritoid. This suggests a reversal in Fe-Mg partitioning between Fe-Mg carpholite and chlorite at temperatures below or close to those of the breakdown of kaolinite + quartz to pyrophyllite and at X_Mg= 0.35.
Phase relations and mineral equilibria indicate that the P-T conditions of formation of the Fe-Mg-carpholite-bearing rocks of NE Oman range from 280–315° C, 3–6 kbar for the structurally highest units to 325–440° C, 6–9.5 kbar for the deepest units, indicating a systematic down-section increase in metamorphic grade. Textural relations in these rocks, interpreted in the context of pertinent equilibria, are consistent with the clockwise P-T paths previously constrained for these units from petrological studies of interlayered isofacial mafic rocks.     

Chemographic analysis of assemblages involving pyrophyllite, chloritoid, chlorite, kaolinite, kyanite, quartz: application to metapelites in the Witwatersrand goldfields, South Africa

The Witwatersrand goldfields contain abundant assemblages that include pyrophyllite, chloritoid, chlorite, kaolinite and/or kyanite, with quartz. A chemographic analysis of the system Fe(Mg)-Al-Si-O-H involving these minerals yields 22 potential phase diagrams. Using orientation criteria and thermodynamic calculations as further constraints, this list has been reduced to three possible diagrams. New thermodynamic data favour one of these in particular.
This chemographic analysis demonstrates that formation of chloritoid is not restricted to the breakdown reaction of kaolinite plus chlorite in the F(M)ASH system, as stated by previous studies, but could be from pyrophyllite + chlorite → chloritoid + quartz + H₂O.
The metamorphic temperature variation between Witwatersrand goldfields exceeded 65 C, based on chlorite and chloritoid compositions. The lower and upper pressure limits are constrained by the andalusite to kyanite, and the sudoite/chlorite to carpholite boundaries, i.e. 1.5–2.8, and 7 kbar, respectively. The widespread pyrophyllite, chlorite and Fe-chloritoid in all the Witwatersrand goldfields, and the local occurrence of sudoite indicate a consistent low-pressure environment in which Mg-chloritoid would not be stable.     

Metastable growth of corundum adjacent to quartz in a spinel-bearing quartzite from the Archaean Napier Complex, Antarctica

In a granulite-facies spinel-bearing quartzite, corundum, orthopyroxene and sapphirine (and rarely cordierite and sillimanite) form partial rims separating spinel from quartz. Textures indicate the reactions:
spinel + quartz = orthopyroxene + corundum, and
spinel + quartz = orthopyroxene + sapphirine.
Thus, corundum and sapphirine are produced by reactions involving quartz. The low Al-content of the orthopyroxene (0.5–2.8 wt %) and low values for Mg–Fe distribution coefficient for spinel–sapphirine and spinel–orthopyroxene reflect low-temperature conditions during formation of the reaction products. Absence of zoning in spinel and a constant Mg–Fe distribution coefficient for spinel–sapphirine and spinel–orthopyroxene, over a compositional range, indicate Mg–Fe equilibration. It is suggested that stable reactions such as spinel + quartz = cordierite or spinel + quartz = garnet + sillimanite were over-stepped and that metastable reactions give rise to the anomalous juxtaposition of corundum + quartz.     

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.     

Interlayer and Si content of phengite in HP–LT carpholite-bearing metapelites

Phengite occurring along with carpholite±lawsonite and/or chloritoid in HP–LT domains shows not only variable Si–(Mg+Fe) contents, but also variable interlayer contents (IC). To determine whether these chemical variations are coherently related to variation in P–T conditions on a regional scale, c. 100 rock samples were sampled in metapelites metamorphosed at conditions varying from 350 °C, 8 to 12 kbar to 450–500 °C, 18 to 20 kbar (Schistes Lustrés complex, franco‐italian Western Alps). Based on microstructural and habit criteria, four types of phengite were differentiated that are related either to the rock mineralogy (carpholite vs chloritoid bearing samples) or correspond to various generations of phengite occurring in the same rock sample or thin section. Microprobe analyses reveal that each type of phengite is characterized by a specific composition and that phengite associated with carpholite has a lower interlayer content than phengite associated with chloritoid. The successive generations of retrograde phengite overgrowing carpholite point to a large decrease of interlayer content (c. 0.9–0.7 pfu) and (Fe+Mg) content (c. 0.25–0 pfu) with decreasing P–T conditions. This change is best accounted for by a gradual increase of the pyrophyllite component. In contrast, phengite from higher‐temperature, chloritoid‐bearing rock samples shows an almost constant interlayer content (c. 0.9–0.95 pfu) but a larger decrease of (Fe+Mg) content (c. 0.6–0.1 pfu). Hence, (1) the composition of the different phengite generations occurring (metastably) in the same rock sample may be used to retrieve points in P–T loops and (2) the pyrophyllitic substitution in phengite is large at low‐temperature conditions and cannot be ignored. Thermobarometric estimates based on the Si‐content alone will therefore result in pressure over‐estimates. We propose a tentative location of the phengite Si and IC isopleths in P–T space which could allow a direct determination of the P–T conditions in carpholite‐bearing rocks. Especially in some carpholite‐bearing rocks, new thermodynamic models accounting for tschermak and pyrophyllitic substitution are also required prior to making reliable thermobarometric estimates in HP‐LT metapelites.     

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.     

Petrology of pelitic schists in the oligoclase-biotite zone of the Sanbagawa metamorphic terrain, Japan: phase equilibria in the highest grade zone of a high-pressure intermediate type of metamorphic belt

The oligoclase-biotite zone of the Bessi area, central Shikoku is characterized by sodic plagioclase (X_Ca= 0.10–0.28)-bearing assemblages in pelitic schists, and represents the highest-grade zone of the Sanbagawa metamorphic terrain. Mineral assemblages in pelitic schists of this zone, all with quartz, sodic plagioclase, muscovite and clinozoisite (or zoisite), are garnet + biotite + chlorite + paragonite, garnet + biotite + hornblende + chlorite, and partial assemblages of these two types. Correlations between mineral compositions, mineral assemblages and mineral stability data assuming PH₂O = P_solid suggests that metamorphic conditions of this zone are about 610 ± 25°C and 10 ± 1 kbar.
Based upon a comparative study of mineralogy and chemistry of pelitic schists in the oligoclase-biotite zone of the Sanbagawa terrain with those in the New Caledonia omphacite zone as an example of a typical high-pressure type of metamorphic belt and with those in a generalized'upper staurolite zone'as an example of a medium-pressure type of metamorphic belt, progressive assemblages within these three zones can be related by reactions such as:     

Cordierite-bearing schists and gneisses from Timor, eastern Indonesia: P-T conditions of metamorphism and tectonic implications

In the Boi Massif of Western Timor the Mutis Complex, which is equivalent to the Lolotoi Complex of East Timor, is composed of two lithostratigraphical components: various basement schists and gneisses; and the dismembered remnants of an ophiolite. Cordierite-bearing pelitic schists and gneisses carry an early mineral assemblage of biotite + garnet + plagioclase + Al-silicate, but contain no prograde muscovite; sillimanite occurs in a textural mode which suggests that it replaced and pseudomorphed kyanite at an early stage and some specimens of pelitic schist contain tiny kyanite relics in plagioclase. Textural relations between, and mineral chemistries of, ferro-magnesian phases in these pelitic chists and gneisses suggest that two discontinuous reactions and additional continuous compositional changes have been overstepped, possibly with concomitant anatexis, as a result of decrease in P_load during high temperature metamorphism. The simplified reactions are: garnet and/or biotite + sillimanite + quartz + cordierite + hercynite + ilmenite + excess components. P-T conditions during the development of the early mineral assemblage in the pelitic gneisses are estimated to have been P + 10 kbar and T > 750°C, based upon the plagioclase-garnet-Al-silicate-quartz geobarometer and the garnet-biotite geothermometer. P-T conditions during the subsequent development of cordierite-bearing mineral assemblages in the pelitic gneisses are estimated to have been P + 5 kbar and T + 700°C with X_H2O < 0.5, based upon the Fe content of cordierite occurring in the assemblage quartz + plagioclase + sillimanite + biotite + garnet + cordierite coexisting with melt. Final equilibration between some of the phases suggests that conditions dropped to P > 2.3 kbar and T > 600°C. A similar exhumation P-T path is suggested for the pelitic schists with early metamorphic conditions of P > 6.2 kbar and T > 745°C and subsequent development of cordierite under conditions in the range P = 3-4 kbar and T = 600-700°C. The tectonic implications of these P-T estimates are discussed and it is concluded that the P-T path followed by these rocks was caused by decompression during rifting and synmetamorphic ophiolite emplacement resulting from processes during the initiation and development of a convergent plate junction located in Southeast Asia during late Jurassic to Cretaceous time.     

Manganiferous schists and their origin,Hidaka Mountains,Hokkaido, Japan

Manganiferous quartz-mica schists (4 m in stratigraphic thickness) overlie epidote amphibolite in the Chiroro River area, Hidaka Mountains, Hokkaido. The schist layers have a considerable range of A/F ratios and bulk oxidation ratios which vary from 21.5 to 100. Manganese contents are from 4 to 30 times higher than that of the average shale with 0.09% MnO. The schists are essentially quartz-white mica-biotite-Mn garnet-tourmaline-±epidote-magnetite assemblages. A highly oxidized layer (5–8 cm thick) 95 cm above the epidote amphibolite contact is characterized by viridine-piemontite-spessartine-Mn white mica-Mn tourmaline-Ti-Mn haematite indicative of both high initial manganese content and very high f _O2 conditions of recrystallization.Viridine contains up to 17 mol% Mn³⁺SiO₅ and coexists with piemontite with between 13.6 and 15.4 wt% Mn₂O₃. Mn-poor-Fe-rich (Ps₃₂) epidote occurs in the less oxidized schist enclosing the viridine-piemontite bearing seam. Garnets vary widely in composition with end member variations (mol%) of Spess_22.9–80.5; And_0.2–11.7; Alm_1.1–57.1; Pyr_2.0–12.2; Gross_7.0–49.0. The more manganiferous garnets occur in rocks with higher oxidation ratios while almandiferous varieties occur in schists with low oxidation ratios. Biotite ranges from green to red-brown varieties (increasing Ti and Fe) with Mg/ (Mg+Fe) ratios varying from 56 to 48. Ten to fifteen percent octahedral R²⁺ is replaced by Al indicating a trend towards eastonite-siderophyllite. The white micas deviate only slightly from dioctahedral stoichiometry but have up to 25% of octahedral sites occupied by Fe, Mg and to a lesser extent Mn and Ti as R²⁺ Si⁴⁺2Al³⁺ and in highly oxidized rocks as (Fe,Mn)³⁺Al³⁺. The white mica in the highly oxidized viridine-piemontite schist is pale pinkishorange, exhibits reverse pleochroism, and has between 0.30 and 0.43 wt% Mn₂O₃.There is a close comparison, both in terms of stratigraphic thickness and Fe-Mn variation, between the Chiroro schist sequence and many oceanic cores so that the bulk chemistry and mineralogy of the pelitic schists is largely an extension of the original Eh-pH conditions of hemipelagic sedimentation and post-depositional adjustments during diagenesis. The thin viridine-piemontite bearing schist is correlated with an oxidized, Fe-Mn rich layer commonly found in present day oceanic cores. The viridine presumably formed by reaction of original ferro-manganese microgranules and clay minerals. Halmrolytic alteration of the underlying metabasalt resulted in leaching of Mn and Fe (in particular) into the overlying sediments and the formation of concentrations of haematite — manganese oxide — Mn garnet along the schist-epidote amphibolite contact.Estimation of the P-T conditions of metamorphism from the phase relations and compositions in the epidote amphibolite associated with the manganiferous schist gives T °C = 530560 and a minimum P _fluid > 3 kb which corresponds to the epidote amphibolite facies of Barrovian-type terrains.This paper is dedicated to Professor Kenzo Yagi on the occasion of his retirement from the Chair of Mineralogy, Department of Geology and Mineralogy, Hokkaido University, Sapporo, Japan     

Metamorphic P–T Paths from pelitic schists and greenstones from the south-west Tauern Window, Eastern Alps

Abstract Petrological data from intercalated pelitic schists and greenstones are used to construct a pressure–temperature path followed by the Upper Schieferhülle (USH) series during progressive metamorphism and uplift in the south-west Tauern Window, Italy. Pseudomorphs of Al–epidote + Fe-epidote + albite + oligoclase + chlorite after lawsonite and data on amphibole crystal chemistry indicate early metamorphism in the lawsonite-albite-chlorite subfacies of the blueschist facies at P ± 7–8 kbar. Geothermometry and geobarometry yield conditions of final equilibration of the matrix assemblage of 475±25°C, 5–6 kbar; calculations with plagioclase and phengite inclusions in garnet indicate early garnet growth at pressures of ∼ 7.5 kbar. Garnet zoning patterns are complex and reversals in zoning can be correlated between samples. Thermodynamic modelling of these zoning profiles implies garnet growth in response to four distinct phases of tectonic activity. Fluid inclusion data from coexisting immiscible H₂O–CO₂–NaCl fluids constrain the uplift path to have passed through temperatures of 380 + 30°C at 1.3 + 0.2 kbar.
There is no evidence for metamorphism of USH at pressures greater than ∼ 7.5 kbar in this area of the Tauern Window. This is in contrast to pressures of ± 10 kbar recorded in the Lower Schieferhülle only 2–3 km across strike. A history of differential uplift and thinning of the intervening section during metamorphism is necessary to reconcile the P–T data obtained from these adjacent tectonic units.     

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.     

Multistage growth of Fe–Mg–carpholite and Fe–Mg–chloritoid,from field evidence to thermodynamic modelling

We provide new insights into the prograde evolution of HP/LT metasedimentary rocks on the basis of detailed petrologic examination, element-partitioning analysis, and thermodynamic modelling of well-preserved Fe–Mg–carpholite- and Fe–Mg–chloritoid-bearing rocks from the Afyon Zone (Anatolia). We document continuous and discontinuous compositional (ferromagnesian substitution) zoning of carpholite (overall X _Mg = 0.27–0.73) and chloritoid (overall X _Mg = 0.07–0.30), as well as clear equilibrium and disequilibrium (i.e., reaction-related) textures involving carpholite and chloritoid, which consistently account for the consistent enrichment in Mg of both minerals through time, and the progressive replacement of carpholite by chloritoid. Mg/Fe distribution coefficients calculated between carpholite and chloritoid vary widely within samples (2.2–20.0). Among this range, only values of 7–11 correlate with equilibrium textures, in agreement with data from the literature. Equilibrium phase diagrams for metapelitic compositions are calculated using a newly modified thermodynamic dataset, including most recent data for carpholite, chloritoid, chlorite, and white mica, as well as further refinements for Fe–carpholite, and both chloritoid end-members, as required to reproduce accurately petrologic observations (phase relations, experimental constraints, Mg/Fe partitioning). Modelling reveals that Mg/Fe partitioning between carpholite and chloritoid is greatly sensitive to temperature and calls for a future evaluation of possible use as a thermometer. In addition, calculations show significant effective bulk composition changes during prograde metamorphism due to the fractionation of chloritoid formed at the expense of carpholite. We retrieve P–T conditions for several carpholite and chloritoid growth stages (1) during prograde stages using unfractionated, bulk-rock XRF analyses, and (2) at peak conditions using compositions fractionated for chloritoid. The P–T paths reconstructed for the Kütahya and Afyon areas shed light on contrasting temperature conditions for these areas during prograde and peak stages.     

Amphibole composition as an indicator of subtle grade variation in epidote-glaucophane schists

Abstract The paragenetic relations of epidote-glaucophane schists are described in terms of the system Al₂O₃-Fe₂O₃-Fe₂O₃-MgO-CaO with excess of quartz, albite and epidote. If alkali-amphibole is free from Ca and Al^IV, its composition when associated with epidote is invariant, univariant or divariant at a given pressure and temperature on Miyashiro's (1957) diagram of alkali-amphibole solid solution if it is also associated, respectively, with three, two or one additional minerals in the system.
Using a group of epidote-glaucophane schists from the Kotu area of the Sanbagawa metamor-phic belt in Shlkoku, Japan (isophysical compositional),univariant boundary lines were determined for the assemblages that, in addition to the ubiquitous quartz + albite + phengitic mica, contain hematite + chlorite, garnet + chlorite and actinolite + chlorite, respectively. The slopes of the univariant boundary lines obtained from petrographical data are in good agreement with those calculated in a model system.
The positions of isophysical univariant boundary lines on the amphibole compositional diagram serve to distinguish the grade of metamorphism among the rocks of the same mineral facies. The hematite-chlorite univariant boundary line can be used to divide the zone of epidote-glaucophane schists of the Sanbagawa metamorphic belt into three, and the garnet-chlorite-paragonite invariant equilibrium can be used to divide the epidote zone of New Caledonia into three.     

Chemistry of micas and chlorite in Proterozoic acid metavolcanics and associated rocks from the Hästefält area,Norberg ore district,central Sweden

Microprobe analyses are performed on micas (biotite, muscovite and phlogopite) and chlorite from 1.9–1.8 Ga acid K- or Na-rich metavolcanics, cordierit-emica schists and manganiferous rocks from the Hästefält area in central Sweden. The results indicate that Fe-rich biotites and muscovites containing 10 to 25% celadonite and/or pyrophyllite are common in the K- and Na-rich metavolcanics. In the cordierite-mica schists the biotites are Mg-rich and the muscovites contain less than 10% celadonite and/or pyrophyllite. The predominant mica in the manganiferous rocks are phlogopite and less frequent rather pure muscovite. The chlorites show a wide range in composition, but principally those occurring in the K- and Na-rich metavolcanics are brunsvigite and diabantite and those in the cordierite-mica schists and the manganiferous rocks are mainly sheridanite and clinochlore. The chlorites of the manganiferous rocks show enrichment in Mn compared to those in other rock types. In general the compositional variations in the micas and less commonly chlorites are strongly controlled by rock type and fluid chemistry, particularly with respect to the ratio of FeO/(FeO+MgO). Estimates of maximum prograde metamorphic temperature, based on phyllosilicates and co-existing cordierite and garnets, indicate a value of up to 500° C.     

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.     

Chloritoid from low-grade schists. Singhbhum,Eastern India

Chloritoid-sericite schists from the chlorite zone of the regionally metamorphosed Singhbhum anticlinorium in Eastern India are described with regard to the formation of chloritoid during prograde metamorphism — the main stage of its crystallisation was coeval with the movement. The movements accompanying metamorphism have had a marked effect on the lattice orientation of this mineral, so that its crystallographic axis is roughly parallel to the regional fold axis. In one case chloritoid appears to be in stable association with hematite, i.e. it persists beyond the magnetite-hematite equilibrium, which is probably a local effect due to a slight rise in oxygen partial pressure in the last stages of metamorphism. The occurrence of phengitic mica in these schists is suggestive of high total pressures and high water pressures.     

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.     

Fluid heterogeneities and hornblende stability in interlayered graphitic and nongraphitic schists (Tauern Window,Eastern Alps)

The assemblage hornblende+white mica occurs in graphite-free schists at two localities in the southwest corner of the Tauern Window, Eastern Alps. In interbedded graphitic layers (1 mm to 1 m thick), however, hornblende is typically replaced by pseudomorphs of biotite+plagioclase +epidote±chlorite+staurolite in the presence of white mica. Garnets adjacent to these pseudomorphs have pronounced growth discontinuities near their rims, in contrast to the continuously zoned garnets in nongraphitic layers. These observations imply that reactions of the type hbl+white micagar+bio+plag+epid±chl±staur +H₂O occurred in the graphitic samples, but that hbl+white mica remained stable in graphite-free layers.Calculation of the equilibrium constants for solid phases in five dehydration equilibria at locality 1 indicates thata(H₂O) in the nongraphitic layers was 6 to 11 times greater thana(H₂O) in the graphitic layers. Similar calculations involving six dehydration equilibria at locality 2 show no difference ina(H₂O) between layers at the conditions of final equilibration. Initial differences in fluid composition maintained between the graphitic and nongraphitic layers caused the hbl+white mica reaction to occur at differentP-T conditions in different horizons of the schists.These data indicate that systematic differences in fluid composition were generated during metamorphism of the interlayered graphitic and non-graphitic schists but were subsequently homogenized at locality 2. The heterogeneities could initially have been produced while the rocks were in theP-T field of CO₂-H₂O immiscibility. Development of a penetrative, layer-parallel shear foliation at this time would have prevented subsequent mixing of the fluids across layers after temperatures exceeded the consolute temperature in the CO₂-H₂O system. Late-stage homogenization of fluids at locality 2 is thought to reflect loss of the buffer capacity of the mineral assemblage in response to total consumption of hornblende.     

Pumpellyite–actinolite facies of the Sanbagawa metamorphism

The pumpellyite–actinolite facies proposed by Hashimoto is defined by the common occurrence of the pumpellyite–actinolite assemblage in basic schists. It can help characterize the paragenesis of basic and intermediate bulk compositions, which are common constituents of various low-grade metamorphic areas. The dataset of mutually consistent thermodynamic properties of minerals gives a positive slope for the boundary between the pumpellyite–actinolite and prehnite–pumpellyite facies in P–T space. In the Sanbagawa belt in Japan, the mineral parageneses of hematite-bearing and -free basic schists, as well as pelitic schists have been well documented. The higher temperature limit of this facies is defined by the disappearance of the pumpellyite+epidote+actinolite+chlorite assemblage in hematite-free basic schists with X_Fe3+ of epidote around 0.20–0.25 and the appearance of epidote+actinolite+chlorite assemblage with X^Ep_Fe3+≤0.20. In hematite-bearing basic schists, there is a continuous change of paragenesis to higher grade, epidote–glaucophane or epidote–blueschist facies. In pelitic schists, the albite+lawsonite+chlorite assemblage does occur but only rarely, and its assemblage cannot be used to determine the regional thermal structure. The lower temperature equivalence of the pumpellyite–actinolite assemblage is not observed in the field. The Mikabu Greenstone complex and the northern margin of the Chichibu complex, which are located to the south of the Sanbagawa belt, are characterized by clinopyroxene+chlorite or lawsonite+actinolite assemblages, which are lower temperature assemblages than the pumpellyite+actinolite assemblage. These three metamorphic complexes belong to the same subduction-metamorphic complex. The pumpellyite–actinolite facies or subfacies can be useful to help reveal the field thermal structure of metamorphic complexes     

Metamorphic evolution, mineral chemistry and thermobarometry of schists and orthogneisses hosting ultra-high pressure eclogites in the Dabieshan of central China

As is typical of ultra-high pressure (UHP) terrains, the regional extent of the UHP terrain in the Dabieshan of central China is highly speculative, since the volume of eclogites and paragneisses preserving unequivocal evidence of coesite and/or diamond stability is very small. By contrast, the common garnet (X_Mn=0.18–0.45)–phengite (Si=3.2–3.35)–zoned epidote (Ps_38–97)–biotite–titanite–two feldspars–quartz assemblages in the more extensive orthogneisses have been previously thought to have formed under low P–T conditions of ca. 400±50°C at 4 kbar. However, certain orthogneiss samples preserve garnets with X_Ca up to 0.50, rutile inclusions within titanite or epidote and relict phengite inclusions within epidote with Si contents p.f.u. of up to 3.49 — overlapping with the highest values (3.49–3.62) recorded for phengites in samples of undoubted UHP schists. These and other mineral composition features (such as A-site deficiencies in the highest Si phengites, Na in garnets linked to Y+Yb substitution and Al F Ti₋₁ O₋₁ substitution in titanites) are taken to be pointers towards the orthogneisses having experienced a similar metamorphic evolution to the associated UHP schists and eclogites. Re-evaluated garnet–phengite and garnet–biotite Fe/Mg exchange thermometry and calculated 5 rutile+3 grossular+2SiO₂+H₂O=5 titanite+2 zoisite equilibria indicate that the orthogneisses may indeed have followed a common subduction-related clockwise P–T path with the UHP paragneisses and eclogites through conditions of P_max at ca. 690°C–715°C and 36 kbar to T_max at ca. 710°C–755°C and 18 kbar, prior to extensive re-crystallisation and re-equilibration of these ductile orthogneisses at ca. 400°C–450°C and 6 kbar. The consequential conclusion, that it is no longer necessary to resort to models of tectonic juxtapositioning to explain the spatial association of these Dabieshan orthogneisses with undoubted UHP lithologies, has far-reaching implications for the interpretation of controversial gneiss–eclogite relationships in other UHP metamorphic terrains.