Reaction textures in calc-silicate granulites from the Bolingen Islands, Prydz Bay, East Antarctica: implications for the retrograde P–T path

Calc-silicate granulites from the Bolingen Islands, Prydz Bay, East Antarctica, exhibit a sequence of reaction textures that have been used to elucidate their retrograde P–T path. The highest temperature recorded in the calc-silicates is represented by the wollastonite- and scapolite-bearing assemblages which yield at least 760°C at 6 kbar based on experimental results. The calc-silicates have partially re-equilibrated at lower temperatures (down to 450°C) as evidenced by the successive reactions: (1) wollastonite + scapolite + calcite = garnet + CO₂, (2) wollastonite + CO₂= calcite + quartz, (3) wollastonite + plagioclase = garnet + quartz, (4) scapolite = plagioclase + calcite + quartz, (5) garnet + CO₂+ H₂O = epidote + calcite + quartz, and (6) clinopyroxene + CO₂+ H₂O = tremolite + calcite + quartz.
The reaction sequence observed indicates that a CO₂ was relatively low in the wollastonite-bearing rocks during peak metamorphic conditions, and may have been further lowered by local infiltration of H₂O from the surrounding migmatitic gneisses on cooling. Fluid activities in the Bolingen calc-silicates were probably locally variable during the granulite facies metamorphism, and large-scale CO₂ advection did not occur.
A retrograde P–T path, from the sillimanite stability field ( c. 760°C at 6 kbar) into the andalusite stability field ( c. 450°C at <3 kbar), is suggested by the occurrence of secondary andalusite in an adjacent cordierite–sillimanite gneiss in which sillimanite occurs as inclusions in cordierite.     

Proterozoic low-pressure/high-temperature metamorphism and an anticlockwise P–T–t path for the Hazeldene area, Mount Isa Inlier, Queensland, Australia

In the Hazeldene area, situated in the Mount Isa Inlier, Queensland, the metamorphic grade changes from chlorite zone, through biotite and cordierite zones, to sillimanite/K-feldspar zone.
Microstructural studies of rocks near the sillimanite isograd demonstrate that cordierite grew early during the development of a steep foliation (S2), was replaced by biotite, andalusite and sillimanite at the metamorphic peak late in S2, and in turn by kyanite + chlorite adjacent to localized small post-D2 shear zones. Although the anticlockwise P–T–t path is well defined, the precise P–T conditions are uncertain because of problems with experimental and thermodynamic data. The best estimate for the metamorphic peak for rocks close to the sillimanite isograd is around 600° C at 4 kbar.
The metamorphism has been dated at 1544 Ma, and was synchronous with a major crustal shortening event. Because proposed extensional events occurred more than 60 Ma earlier, their contribution to the peak metamorphic thermal perturbation would have been insignificant. The syn-metamorphic Mica Creek Pegmatites, the abundance of high heat-producing elements in the nearby pre-D2 Sybella Granite, and advective heat by fluids which caused considerable metasomatism in the Hazeldene area, may have each contributed to the thermal budget. However, the metamorphic thermal gradient may be 80°C km^-1 or higher, strongly suggesting a local magmatic control. As none are known in the area, such syn-metamorphic plutons would have to lie beneath the exposed high-grade rocks.     

Two-stage decompression in orthopyroxene–sillimanite granulites from Forefinger Point, Enderby Land, Antarctica: implications for the evolution of the Archaean Napier Complex

Magnesian metapelites of probable Archaean age from Forefinger Point, SW Enderby Land, East Antarctica, contain very-high-temperature granulite facies mineral assemblages, which include orthopyroxene (8–9.5 wt% Al₂O₃)–sillimanite ± garnet ± quartz ± K-feldspar, that formed at 10 ± 1.5 kbar and 950 ± 50°C. These assemblages are overprinted by symplectite and corona reaction textures involving sapphirine, orthopyroxene (6–7 wt% Al₂O₃), cordierite and sometimes spinel at the expense of porphyroblastic garnet or earlier orthopyroxene–sillimanite. These textures mainly pre-date the development of coarse biotite at the expense of initial mesoperthite, and the subsequent formation of orthopyroxene (4–6 wt% Al₂O₃)–cordierite–plagioclase rinds on late biotite.
The early reaction textures indicate a period of near-isothermal decompression at temperatures above 900°C. Decompression from 10 ± 1.5 kbar to 7–8 kbar was succeeded by biotite formation at significantly lower temperatures (800–850°C) and further decompression to 4.5 ± 1 kbar at 700–800°C.
The later parts of this P–T evolution can be ascribed to the overprinting and reworking of the Forefinger Point granulites by the Late-Proterozoic ( c . 1000 Ma) Rayner Complex metamorphism, but the age and timing of the early high-temperature decompression is not known. It is speculated that this initial decompression is of Archaean age and therefore records thinning of the crust of the Napier Complex following crustal thickening by tectonic or magmatic mechanisms and preceding the generally wellpreserved post-deformational near-isobaric cooling history of this terrain.     

Chemographic relationships of biotite and cordierite in the McGerrigle thermal aureole, Gaspé, Quebec

Abstract Biotite and cordierite occur in a 1-km wide zone of pelitic hornfelses around the McGerrigle pluton. These phases display systematic changes in X _Fe that can be attributed to continuous reactions involving chlorite or andalusite in the system KFMASH. Through much of the zone biotite and cordierite were products of the 'breakdown'of chlorite. Close to the pluton this continuous reaction was terminated by a discontinuous reaction that introduced andalusite. Pelites which interdigitate with apophyses of the intrusive at the pluton margin contain assemblages that record a continuous reaction between biotite, cordierite, andalusite, muscovite, and quartz or, alternatively, the discontinuous breakdown of muscovite and quartz to K-feldspar and andalusite.
The mole fraction of Fe in biotite and cordierite increased significantly with the progress of the first continuous reaction and apparently decreased during the second continuous reaction. The K _D of Fe-Mg between the minerals decreased and apparently increased, respectively, during the two reactions.
Biotite-cordierite-chlorite assemblages are interpreted to have been stable at temperatures between 525° C and 615° C and biotite-cordierite-andalusite assemblages stable at temperatures between 615° C and 635° C. The confining pressure was estimated to have been < 2 kbar.
The results of this study suggest that the K _D of Fe-Mg between biotite and cordierite is a function of temperature, the Fe-Mg exchange characteristics of the controlling continuous reaction and non-ideal mixing of Fe and Mg.     

Petrology of spinel granulites from Araku, Eastern Ghats, India, and a petrogenetic grid for sapphirine-free rocks in the system FMAS

Abstract Spinel-quartz-cordierite and spinel-quartz are found as relic prograde assemblages in Fe-rich granulites from the Araku area, Eastern Ghats belt, India. Subsequent reactions produced orthopyroxene + sillimanite in the former association and garnet + sillimanite in the latter. The first reaction is univariant in the FMAS system, but is trivariant in the present case because of the presence of Zn and Fe³⁺ in spinel. The second reaction also has high variance because of Zn and Fe³⁺, but also because of the presence of Ca in garnet. Thermobarometry shows that the metamorphic conditions were approximately 950° C and 8.5 kbar and the fo ₂ was near the NNO buffer. In Fe-rich bulk compositions and low- P -high- T conditions of metamorphism, two of the univariant reactions around the invariant point [Sa], namely (Sa, Hy) and (Sa, Cd), change topology due to reverse partitioning of Fe-Mg between coexisting garnet and spinel. An alternative partial petrogenetic grid in the system FMAS is constructed for such conditions and is applied satisfactorily to several sapphirine-free spinel granulites. It is shown that bulk composition ( X _Fe and Zn) exerts greater control on the stability of spinel + quartz than fo ₂. The effect of the presence of Zn and Fe³⁺ in spinel on the proposed grid is evaluated. Reaction textures in the Araku spinel granulites can be explained from the petrogenetic grid as due to near-isobaric cooling.     

Progressive sequence of reactions of the Ryoke metamorphism in the Yanai district, southwest Japan: the formation of cordierite

The compositions of biotite and muscovite were examined in terms of the paragenesis and the metamorphic grade in low- to medium-grade pelitic rocks of the Ryoke metamorphism in the Yanai district, southwest Japan. The biotite and muscovite that coexist with K-feldspar have a higher K component in an A'KF diagram than those in rocks lacking K-feldspar. This fact reflects an increase in the K₂O content in muscovite, but in biotite it reflects an increase of not only the K₂O content but also of the octahedral vacancy.
At higher metamorphic grade beyond the cordierite isograd, where cordierite coexists with neither chlorite nor K-feldspar, the biotite shows an increase in illite, K Aliv □xii−1 Si−1, and Tschermak components, Alvi Aliv R+−1 Si−1, where □xii and R+ denote the interlayer vacancy and (Fe+Mg+Mn), respectively. A reaction to define the cordierite isograd is proposed by treating this chemical change as being responsible for the first appearance of cordierite, i.e. K,Al-poor biotite+phengitic muscovite=K,Al-rich biotite+cordierite+quartz+water .By treating this as a key reaction in medium-grade metamorphism, a set of reaction in a progressive metamorphism is established for the Ryoke metamorphism, a typical low-pressure type metamorphism. Some textures in one of the high-grade areas, the K-feldspar-cordierite zone, suggest that a further two prograde reactions have taken place, i.e. andalusite+biotite+quartz=cordierite+K-feldspar+water
and   andalusite=sillimanite.quartz=cordierite+K-feldspar+water
This implies that this zone probably has a P–T  path involving isobaric heating.     

A second natural occurrence of yoderite

A second example of yoderite has been discovered in whiteschists from the Southern Chewore Hills of northern Zimbabwe. The mineral is pale green in colour and occurs in an equilibrium assemblage with talc+chlorite+kyanite+dravite+hematite. There is no quartz present. Recalculated microprobe analyses give a structural formula of Mg₂Al_5.7Fe_0.3Si₄O₁₈(OH)₂, similar to that obtained for the type locality at Mautia Hill, Tanzania, i.e. Mg₂Al_5.6Fe_0.4Si₄O₁₈(OH)₂. Textural relationships and relative proportions of minerals suggest that the yoderite was formed by reaction between talc, chlorite, kyanite and hematite. Experimental evidence suggests high-water-pressure metamorphic conditions at temperatures exceeding a reaction curve that extends between 13  kbar at 590  °C and 21  kbar at 650  °C. The yoderite-bearing whiteschist is associated with a 1.4  Ga dismembered ophiolite. It is proposed that this yoderite occurrence is associated with a relict subduction/suture zone.     

Continuous reactions between biotite, garnet, staurolite, kyanite-sillimanite-andalusite and P-T-time-deformation path in micaschists from the estuary of the river Vilaine, South Brittany, France

Abstract Microprobe analysis of the continuous chemical evolution of coexisting biotite-garnet and biotite-garnet-staurolite has been undertaken from interbedded micaschists of the volcanodetrital group of the Vilaine. A thermobarometric study using pertinent mineralogical equilibria reveals a complex P-T evolution, continuous throughout time, from high pressure, medium temperature (kyanite zone) to medium pressure, high temperature (sillimanite zone), then low pressure, medium temperature (andalusite zone). The T, P, f_H2o and X_H2o variations have been calculated from coexisting biotite-garnet pairs, and from the equilibria: paragonite (in white mica) + quartz ± albite (in plagioclase) + Al silicate + H₂O; and, 3 anorthite ± grossular + 2 Alsilicate + quartz. The P-T evolution is correlated with the continuous change in composition of minerals (using P–X_Mg and T–X_Mg diagrams) and with the evolution of assemblages. This continuous P-T-time evolution, correlated with the successive formation of S₁-S₂ foliations, allows us to propose a P-T-time-deformation path for the micaschists and to relate the growth of its mineral components to tectonic processes.     

TEM observations of several spinel-garnet assemblies: toward the rheology of the transition zone

In order to better identify the mineral phase which controls the rheology of the transition zone (between 410 and 660 km depth) transmission electron microscopy observations were made on several coexisting spinel-garnet assemblies: alkremite xenolith; pyrope-rich – MgO:1.1Al₂O₃ spinel assembly deformed at 1173K, 800 MPa in a Griggs apparatus; (Mg,Fe)₃(Al,Mg,Si)₂Si₃O₁₂ majorite – (Mg,Fe)₂SiO₄ spinel assembly synthesized in a laser heated diamond anvil cell. It was found that garnet crystals systematically remain undeformed while spinel crystals are plastically deformed. These results are in accord with the assumption that the rheology of majorite is stronger than the rheology of spinel, in the conditions of the transition zone.     

The muscovite-melt bathograd and low-P isograd suites in north-central Wopmay Orogen, Northwest Territories, Canada

In north-central Wopmay Orogen, syntectonic low-P(Buchan-type) suites of mineral isograds outline regional metamorphic temperature culminations that are associated, at the higher structural levels, with emplacement of early Proterozoic plutons in the west part of a deformed and eastward transported continental margin prism. The mapped isograds mark the first occurrence of biotite, staurolite, andalusite, sillimanite, sillimanite-K feldspar and K feldspar-plagioclase-quartz ± muscovite (granitic) pods in metapelites, with increasing proximity to the plutons.
Microprobe analyses and field observations have resulted in the formulation of reactions for the 'ideal'pelitic system K₂O-Na₂O-FeO-MgO-Al₂O₃-SiO₂-H₂O-Al₂O₃-SiO₂-H₂O, to account for the various mineral assemblages of each metamorphic zone. A P-T petrogenetic grid showing erosion surface P-T curves for the northern Wopmay Orogen pelites, compiled on the basis of the mapped isograds and the inferred reaction(s) for each metamorphic zone, documents a variation in exposed metamorphic pressure ranging between 2 and 4 kbar.
The configuration of a new bathograd, based on the invariant model reaction sillimanite + K feldspar + plagioclase + biotite + quartz + vapor ± muscovite + liquid and interpolated across three metamorphic suites, is consistent with a major regional structure culmination and with independently determined pressures obtained from anorthite-grossular-quartz-Al₂SiO₅ geobarometry. The positive correlation between the configuration of the bathograd and the structural and pressure culmination points to the pressure-dependence of anatectic-granitic-pod mineral associations.     

Chloritoid-bearing rocks associated with blueschists and eclogites, northern New Caledonia

Abstract Chloritoid-bearing metasedimentary rocks occur in close proximity to blueschists and eclogites in the Tertiary high-pressure metamorphic belt of northern New Caledonia. The typical assemblage of chloritoid-bearing rocks in the epidote zone is quartzchlorite-muscovite-garnet-chloritoid. In the omphacite zone, epidote is an additional member of the chloritoid-bearing assemblage. Paragonite is rare, plagioclase was not detected, and rutile and ilmenite are the Fe-Ti oxide phases. Chloritoid-glaucophane is not a common assemblage. Chloritoid-bearing rocks have relatively low (Ca+K+Na)/Al ratios and the chloritoids are relatively Mg-rich with Mg/ (Mg+Fe) up to about 0.4. A comparison of the mineral assemblages and mineral chemistry with experimental and computed phase equilibria suggest an upper temperature limit near 560° C in the omphacite zone and a minimum temperature limit near 450° C at 10 kbar. An empirical garnet-chlorite Fe-Mg exchange thermometer does not yield consistent results for the higher-grade rocks, suggesting T s ranging from 390 to 535° C in the omphacite zone and 420–465° C in the epidote zone. The distribution coefficient K _D = (Fe/Mg)_ctd/(Fe/Mg)_chl for chloritoid and chlorite ranges from 3.9 to 6.4, values which are lower than those (=10) from lower greenschist facies rocks, but are near those of upper greenschist facies and albite-epidote amphibolite facies.     

Controls on the first appearance of jadeitic pyroxene, northern Diablo Range, California

A reaction producing jadeitic pyroxene in metagreywackes of the northern Diablo Range has been identified on the basis of mineral distribution, isograd patterns and composition of coexisting minerals. The appearance of jadeitic pyroxene (∼Jd₈₀) is closely followed by the disappearance of pumpellyite, which indicates that pumpellyite plays a major role in the pyroxene-producing reaction. A new projection from hematite, lawsonite, chlorite, quartz and H₂O on to the NaAlO₂-FeO-MgO ternary confirms the role of pumpellyite in pyroxene production and suggests a reaction of the form: 1.00 pumpellyite + 0.31 chlorite + 8.71 albite + 0.70 hematite + 2.00 H₂O = 8.54 jadeite + 0.57 glaucophane + 3.09 lawsonite + 5.26 quartz. Metagreywackes of the northern Diablo Range were metamorphosed under conditions of P _H2O= P _total at 200-300 °C and 7.5-10.0 kbar. Despite the low temperatures attained during metamorphism, the assumption of equilibrium yields results consistent with field observations and phase relations.     

Sequential growth of cordierite and andalusite porphyroblasts, Cooma Complex, Australia: microstructural evidence of a prograde reaction

Abstract Low-pressure prograde metamorphism of pelitic rocks in the Cooma Complex, south-east Australia, has produced cordierite-andalusite schists at intermediate grades. The first foliation (S₁) is preserved largely as inclusion trails in cordierite porphyroblasts. Microstructural evidence indicates that the cordierite porphyroblasts grew during the early stages of development of a crenulation-foliation (S₂) and that andalusite porphyroblasts grew during the development of a later crenulation-foliation (S₃). Microstructural evidence also indicates that the andalusite was a product of the prograde reaction: cordierite + muscovite ± andalusite + biotite + quartz. The occurrence of the products of this reaction in 'beard'structures between cordierite microboudins formed by extension in S₃ confirms that the andalusite grew during the development of S₃. The investigation shows that porphyroblast-matrix relationships can preserve the orientation of an early S-surface that has been largely obliterated from the matrix, as well as providing relatively direct evidence of sequential mineral growth and metamorphic reactions.     

Using estimated thermodynamic properties to model accessory phases: the case of tourmaline

Accessory phases and minor components in minerals are commonly ignored in thermodynamic modelling. Such an approach seems unwarranted, as accessory phases can represent a significant element reservoir and minor components can substantially change their host mineral's stability field. However, a lack of thermodynamic data prohibits assessment of these effects. In this contribution, the polyhedron method is used to estimate the thermodynamic properties of tourmaline, a common and widespread accessory phase, stable over a range of P–T–X conditions. The polyhedron method allows Δ H , S , V , C _P and V _m ( T , P ) properties to be estimated from a linear stoichiometric summation over the fractional properties of its polyhedron constituents. To allow for estimates of tourmaline, fractional thermodynamic properties for B^III and B^IV polyhedra were derived. Mixing contributions to molar volume were evaluated and symmetrical mixing parameters derived for Al-Mg, Al-Fe and Al-Li interaction on tourmaline's Y-site and T-site Al-Si interaction. Evaluation of the estimated properties using experimental and natural equilibria between tourmaline and melts, minerals and hydrothermal fluids, shows that reliable semi-quantitative results are obtained. The boron contents in fluids coexisting with tourmaline are calculated to within an order of magnitude of measured content, and where anchor-points are available, agreement improves to within a factor of 2. Including tourmaline in petrogenetic modelling of metamorphic rocks indicates that its presence leads to disappearance of staurolite and garnet, among others, and modifies the X _Mg of coexisting phases, in line with observations on natural rocks.     

Reaction relationships during retrograde metamorphism at Olary, South Australia

Abstract In metapelitic schists of the north-eastern Weekeroo Inliers, Olary Block, Willyama Supergroup, South Australia, syn-S1 and syn-S2 assemblages involving staurolite, garnet, biotite and another mineral, most probably cordierite, were overgrown by large syn-S3 andalusite porphyroblasts, owing to isobaric heating from metamorphic conditions that existed during the development of S2. Conditions during the development of S3 probably just reached the andalusite—sillimanite transition. During the development of S4, at somewhat lower temperatures than those that accompanied the development of S3, the following reaction occurred:
staurolite + chlorite + muscovite ± biotite + andalusite + quartz + H₂O.
The amount of retrogression is controlled primarily by the amount of H₂O added by infiltration. As the syn-S3 matrix assemblage was stable during the development of S4, but the andalusite porphyroblasts were no longer stable with the matrix when H₂O was added, the retrogression is focused in and around the porphyroblasts. With enough H₂O available, and if quartz was consumed before biotite in a porphyroblast, then the following reaction occurred:
staurolite + chlorite + muscovite + corundum ± biotite + andalusite + H₂O.
This reaction allowed corundum inclusions in the andalusite to grow, regardless of the presence of quartz in the matrix assemblage.     

Genesis of monazite and Y zoning in garnet from the Black Hills, South Dakota

The paragenesis of monazite in metapelitic rocks from the contact aureole of the Harney Peak Granite, Black Hills, South Dakota, was investigated using zoning patterns of monazite and garnet, electron microprobe dating of monazite, bulk-rock compositions, and major phase mineral equilibria. The area is characterized by low-pressure and high-temperature metamorphism with metamorphic zones ranging from garnet to sillimanite zones. Garnet porphyroblasts containing euhedral Y annuli are observed from the garnet to sillimanite zones. Although major phase mineral equilibria predict resorption of garnet at the staurolite isograd and regrowth at the andalusite isograd, textural and mass balance analyses suggest that the formation of the Y annuli is not related to the resorption-and-regrowth of garnet having formed instead during garnet growth in the garnet zone. Monazite grains in Black Hills pelites were divided into two generations on the basis of zoning patterns of Y and U: monazite 1 with low-Y and -U and monazite 2 with high-Y and -U. Monazite 1 occurs in the garnet zone and persists into the sillimanite zone as cores shielded by monazite 2 which starts to form in the andalusite zone. Pelites containing garnet porphyroblasts with Y annuli and monazite 1 with patchy Th zoning are more calcic than those with garnet with no Y annuli and monazite with concentric Th zoning. Monazite 1 is attributed to breakdown of allanite in the garnet zone, additionally giving rise to the Y annuli observed in garnet. Monazite 2 grows in the andalusite zone, probably at the expense of garnet and monazite 1 in the andalusite and sillimanite zones. The ages of the two different generations of monazite are within the precision of chemical dating of electron microprobe. The electron microprobe ages of all monazites from the Black Hills show a single ca. 1713 Ma population, close to the intrusion age of the Harney Peak Granite (1715 Ma). This study demonstrates that Y zoning in garnet and monazite are critical to the interpretation of monazite petrogenesis and therefore monazite ages.     

Exhumation during oblique transpression: The Feiran–Solaf region, Egypt

The Feiran–Solaf metamorphic complex of Sinai, Egypt, is one of the highest grade metamorphic complexes of a series of basement domes that crop out throughout the Arabian-Nubian Shield. In the Eastern Desert of Egypt these basement domes have been interpreted as metamorphic core complexes exhumed in extensional settings. For the Feiran–Solaf complex an interpretation of the exhumation mechanism is difficult to obtain with structural arguments as all of its margins are obliterated by post-tectonic granites. Here, metamorphic methods are used to investigate its tectonic history and show that the complex was characterized by a single metamorphic cycle experiencing peak metamorphism at ∼700–750 °C and 7–8 kbar and subsequent isothermal decompression to ∼4–5 kbar, followed by near isobaric cooling to 450 °C. Correlation of this metamorphic evolution with the deformation history shows that peak metamorphism occurred prior to the compressive deformation phase D ₂, while the compressive D ₂ and D ₃ deformation occurred during the near isothermal decompression phase of the P–T loop. We interpret the concurrence of decompression of the P–T path and compression by structural shortening as evidence for the Najd fault system exhuming the complex in an oblique transpressive regime. However, final exhumation from ∼15 km depth must have occurred due to an unrelated mechanism.     

Phase relations in andalusite-sillimanite type Fe-rich metapelites: Tono contact metamorphic aureole, northeast Japan

Mineral assemblages in metapelites of the contact aureole of the Tono granodiorite mass, northeast Japan, change systematically during progressive metamorphism along an isobaric path at 2-3 kbar. The bulk rock compositions of metapelites are aluminous with A' values on an AFM projection larger than that of the chlorite join. The metapelites commonly contain paragonite in the low-grade zone. With increasing temperatures, andalusite is formed by the breakdown of paragonite. The importance of pyrophyllite as a source of Al₂SiO₅ polymorphs is limited in typical pelitic rocks.
The most common type of metapelite in the study area has FeO/(FeO + MgO) = 0.5–0.6, and develops assemblages involving chlorite, andalusite, biotite, cordierite, K-feldspar, sillimanite and almandine, with paragenetic changes similar to other andalusite-sillimanite type aureoles. Rocks with FeO/(FeO + MgO) > 0.8 progressively develop chloritoid-bearing assemblages from Bt-Chl-Cld, And-Bt-Cld, to And-Bt at temperatures between the breakdown of paragonite and the appearance of cordierite in the more common pelitic rocks in the aureole. The paragenetic relations are explained by a KFMASH univariant reaction of Chl + Cld = And + Bt located to the low-temperature side of the formation of cordierite by the terminal equilibrium of chlorite. A P-T model depicting the relative stability of chloritoid and staurolite at low- and medium-pressure conditions, respectively, is proposed, based on the derived location of the Chl + Cld = And + Bt reaction combined with the theoretical phase relations among biotite, chlorite, chloritoid, garnet and staurolite.     

Stable isotope constraints on the Al2SiO5'triple-point' rocks from the Proterozoic Priest pluton contact aureole, New Mexico, USA

The Priest pluton contact aureole in the Manzano Mountains, central New Mexico preserves evidence for upper amphibolite contact metamorphism and localized retrograde hydrothermal alteration associated with intrusion of the 1.42 Ga Priest pluton. Quartz–garnet and quartz–sillimanite oxygen isotope fractionations in pelitic schist document an increase in the temperatures of metamorphism from 540 °C, at a distance of 1 km from the pluton, to 690 °C at the contact with the pluton. Comparison of calculated temperature estimates with one‐dimensional thermal modelling suggests that background temperatures between 300 and 350 °C existed at the time of intrusion of the Priest pluton. Fibrolite is found within 300 m of the Priest pluton in pelitic and aluminous schist metamorphosed at temperatures >580 °C. Coexisting fibrolite and garnet in pelitic schist are in oxygen isotope equilibrium, suggesting these minerals were stable reaction products during peak metamorphism. The fibrolite‐in isograd is coincident with the staurolite‐out isograd in pelitic schist, and K‐feldspar is not observed with the first occurrence of fibrolite. This suggests that the breakdown of staurolite and not the second sillimanite reaction controls fibrolite growth in staurolite‐bearing pelitic schist. Muscovite‐rich aluminous schist locally preserves the Al₂SiO₅ polymorph triple‐point assemblage – kyanite, andalusite and fibrolite. Andalusite and fibrolite, but not kyanite, are in isotopic equilibrium in the aluminous schist. Co‐nucleation of fibrolite and andalusite at 580 °C in the presence of muscovite and absence of K‐feldspar suggests that univariant growth of andalusite and fibrolite occurred. Kyanite growth occurred during an earlier regional metamorphic event at a temperature nearly 80 °C lower than andalusite and fibrolite growth. Quartz–muscovite fractionations in hydrothermally altered pelitic schist and quartzite are small or negative, suggesting that late isotopic exchange between externally derived fluids and muscovite, but not quartz, occurred after peak contact metamorphism and that hydrothermal alteration in pelitic schist and quartzite occurred below the closure temperature of oxygen self diffusion in quartz (<500 °C).     

Magmatic and hydrothermal processes in the Bouvet Triple Junction Region (South Atlantic)

Results of electron microprobe and microthermometric studies of samples collected from the Bouvet Triple Junction Region (BTJR) during a joint Russian-Italian geological expedition on the R/V Academician Nikolaj Strakhov (1994) have revealed new data on the composition of basaltic magmas and oceanic hydrothermal fluids connected with magmatic processes. Detailed analysis of basaltic glasses shows that the modem Mid-Atlantic Ridge (MAR) rift valley is composed of normal mid-ocean ridge basalts with low concentrations of K₂ O and TiO_z (N-MORB), while its flanks are more enriched with these components approaching E-MORB. A marked influence of the Bouvet hot spot volcanism on magma generation on the South-West Indian Ridge (SWIR) near Bouvet Island is observed. Basaltic melts in this area belong to alkalic and transitional series and have maximum contents of K₂O, TiO₂, H₂O.
Microthermometric analyses of fluid inclusions in the samples from the BTJR have revealed major differences in the oceanic hydrothermal fluid systems on the MAR and near SWIR, which depends on the peculiarities of magma. In the area of the MAR (with dry melts) only H₂O solution inclusions in quartz were found; thus, seawater is probably the only primary source of hydrothermal fluids (NaCl + MgCl₂+ H₂O; T = 170–200°C). In the SWIR area (with the high content of water in melts) syngenetic liquid CO₂ and H₂O solution inclusions in quartz indicate the influence of the magmatic fluid component on the ore-forming water/carbon dioxide solutions (NaCl + CaC1₂+ H₂O + CO₂; T = 200–310 °C; P = 900–1700 bar).