ALBERT

Notes: Abstract A garnet–hornblende Fe–Mg exchange geothermometer has been calibrated against the garnet–clinopyroxene geothermometer of Ellis & Green (1979) using data on coexisting garnet + hornblende + clinopyroxene in amphibolite and granulite facies metamorphic assemblages. Data for the Fe–Mg exchange reaction between garnet and hornblende have been fitted to the equation. In KD=Δ (XCa,g) where KD is the Fe–Mg distribution coefficient, using a robust regression approach, giving a thermometer of the form: with very satisfactory agreement between garnet–hornblende and garnet–clinopyroxene temperatures. The thermometer is applicable below about 850°C to rocks with Mn-poor garnet and common hornblende of widely varying chemistry metamorphosed at low aO2.Application of the garnet–hornblende geothermometer to Dalradian garnet amphibolites gives temperatures in good agreement with those predicted by pelite petrogenetic grids, ranging from 520°C for the lower garnet zone to 565–610°C for the staurolite to kyanite zones. These results suggest that systematic errors introduced by closure temperature problems in the application of the garnet–clinopyroxene geothermometer to the ‘calibration’data set are not serious. Application to ‘eclogitic’garnet amphibolites suggests that garnet and hornblende seldom attain Fe–Mg exchange equilibrium in these rocks.Quartzo-feldspathic and mafic schists of the Pelona Schist on Sierra Pelona, Southern California, were metamorphosed under high pressure greenschist, epidote–amphibolite and (oligoclase) amphibolite facies beneath the Vincent Thrust at pressures deduced to be 10±1 kbar using the phengite geobarometer, and 8–9kbar using the jadeite content of clinopyroxene in equilibrium with oligoclase and quartz. Application of the garnet–hornblende thermometer gives temperatures ranging from about 480°C at the garnet isograd through 570°C at the oligoclase isograd to a maximum of 620–650°C near the thrust. Inverted thermal gradients beneath the Vincent Thrust were in the range 170 to 250°C per km close to the thrust.

Notes: Coexisting Ca-poor and Ca-rich pyroxenes in granulites at Cape Riche, in the Precambrian Albany-Fraser Province, Western Australia, are dominantly chemically homogeneous within individual samples, suggesting a major episode of equilibration. However, occasional grains in a few samples contain exsolved domains interpreted as relics of an earlier, higher-T assemblage. Pyroxene pairs in ten, presumably isothermal, samples from a restricted area are used to (i) assess the suitability of several versions of the two-pyroxene thermometer for application to metamorphic rocks, and (ii) determine the thermal history of the Cape Riche pyroxenes.The various versions of the two-pyroxene thermometer applied to the well-equilibrated homogeneous pyroxene grains show poor to good precision and yield mean temperatures varying widely from 683° to 893°C, in the following order of increasing T: Lindsley (1983; opx version), 683°± 11°C; Kretz (1982; KD version), 705°± 19°C; Ross & Huebner (1975), 709°± 30°C; Kretz (1982; solvus version), 735°± 24°C; Fonarev & Graphchikov (1982; opx version), 〈750°C; Lindsley (1983; cpx version), 784°± 40°C; Fonarev & Graphchikov (1982; cpx version), ~820°± 30°C; Wood & Banno (1973), 849°± 16°C; Powell (1978), 854°± 23°C; Wells (1977), 893°± 10°C. Independent T estimates, based on mafic assemblages and garnet-biotite thermometry, suggest that the major episode of metamorphism occurred at 700-800°C (P ~ 5 kbar). Therefore the Wells, Powell, Wood & Banno and Fonarev & Graphchikov (cpx) temperatures are almost certainly too high. In the absence of a more precise independent T estimate it is difficult to assess the relative merits of the results obtained from the remaining versions of the two-pyroxene thermometer, none of which can be unequivocally demonstrated to be seriously in error, though the Lindsley (opx) T is probably too low. Other significant shortcomings evident in the results include the relatively poor precision obtained from the three methods based on purely graphical representation of the augite limb of the solvus (i.e., the Ross & Huebner, Fonarev & Graphchikov (cpx) and Lindsley (cpx) versions), and the apparent dependence of derived T on Mg/Fe2+ ratio for the Powell, Wood & Banno and Lindsley (cpx) methods.For the bulk compositions of exsolved domains, the different versions of the two-pyroxene thermometer yield mean temperatures 23° to 82°C (overall mean, 65°C) higher than for homogeneous grains in the same samples. These exsolved domains are interpreted as relics of a higher-T (peak?) metamorphic assemblage, rather than an igneous precursor.

Notes: This work presents the results of a fluid inclusion study of an amphibolite-granulite facies transition in West Uusimaa, S.W. Finland. Early fluid-inclusions in the granulite facies area are characteristically carbonic (CO2), in contrast to predominantly aqueous early inclusions in the amphibolite facies area. These early inclusions can be related to peak metamorphic conditions (750-820°C and 3-5 kbar for peak granulite facies metamorphism). Relatively young CO2 inclusions with low densities (〈0.8g/cm3) indicate that the first part of the cooling history of the rocks was characterized by a near isothermal uplift.N2-CH4 inclusions, with compositions ranging between pure CH4 and pure N2 (Raman spectral analysis), were found in the whole area. They are probably syn- or even pre-early inclusions. Only nearly critical homogenizing inclusions have been found (low density). Pressure estimates, based on densities of early fluid inclusions, show that the rapid transition of amphibolite towards granulite facies metamorphism is virtually isobaric. Granulite facies metamorphism in West Uusimaa is a thermal event, probably induced by the influx of hot, CO2-bearing fluids.

Notes: Multisystems of n+k (k 〉 3) phases are very complicated and knowledge of them has suffered as a result. The successful solution of the topological relationships in n+ 3 phase multisystems by Zen (1966, 1967) and Zen & Roseboom (1972) has aroused much interest regarding what will happen in a multisystem of more than n+ 3 phases. Since 1979, some important research results on this topic have been published. These results have expounded the substantial rules governing the appearance of phase relations in phase diagrams of n - k (k 〉 3) phase multisystems. The most significant conclusions include: (1) It is impossible to incorporate all the possible phase relations in an n+k (k 〉 3) phase multisystem in a single closed net. Therefore, it is no longer enough to use only a single closed net to depict the topological relations involved in these types of multisystems. Instead, one or more groups of closed nets, namely the complete system(s) of closed nets are necessary for this purpose. (2) A principle called the Combination Principle has been proposed and proved. It states: Any closed net of one n+k (k 〉 3) phase multisystem must be a combination of two or more distinct n+ 3 order submultisystem closed nets belonging to the given n+k phase multisystem, if it is not one of the n+ 3 order submultisystem closed nets itself. The combination principle provides both a theoretical basis and a practical method for the construction of closed nets and, hence, for the derivation of the real phase diagrams for any n+k (k 〉 3) phase multisystem. (3) A theorem on divariant-assemblage-characteristic-stability-polygons is also important to our understanding of the n+k (k± 3) phase multisystem closed nets. This theorem can be stated as follows: A divariant assemblage of an n+k (k± 3) phase multisystem will be stable in an l-polygon lacking diagonals in an appropriate set of closed-net-diagrams, and this l-polygon may be at least a triangle, and at most a k-polygon. In addition, the closed-net-diagrams of unary and binary n+ 4 phase multisystems derived respectively by Guo (1980b, 1980c, 1981a) and by Roseboom & Zen (1982) have also been summarized. The combination principle is applied to a practical petrological problem in this paper, dealing with 7 phases in the system FeO-Fe2O3-SiO2.

Notes: Abstract The stability of quartz-chloritoid-staurolite-almandine-cordierite and aluminium silicates is used to constrain both metamorphic conditions and pressure-temperature trajectories for two localities within the 2700 Ma Archaean Yilgarn Block in Western Australia. Available experimental data are used to calculate thermodynamic data for a self-consistent set of equilibria between these minerals. A lower amphibolite facies locality from the margin of a lower strain area contains assemblages including quartz-chloritoid-staurolite-garnet-biotite with altered cordierite replacing chloritoid, quartz-staurolite-andalusite, and quartz-cordierite-andalusite-biotite. This locality was heated to 530–560°C in the andalusite field, at 4.2 kbar. A sample from a mid- to upper-amphibolite facies, highly strained locality contains relict staurolite enclosed by andalusite, in turn replaced by cordierite and muscovite with biotite and sillimanite in the matrix. The assemblage was heated isobarically from conditions near the maximum experienced by the lower grade locality of 560°C at 4.2 kbar to temperatures in excess of the andalusite-sillimanite transition but within the quartz plus muscovite stability field (600–650°C). The higher grade locality is close to a granitoid dome and sections based on gravity profiles reveal that this locality is underlain by granitoid at shallow depths. The higher grade metamorphism apparently reflects superposition of the thermal aureole on regional metamorphic conditions similar to those in the lower grade areas.

Notes: Abstract A major system of steep Caledonian shear zones, of regional extent, has been identified in NE Scotland. The shear zones affect a wide range of lithologies, including Argyll and Southern Highland Group Dalradian, ‘Younger Basic’intrusives and their hornfelses, and also the earlier of the more acid intrusions. The observed fabrics and parageneses are consistent with low-pressure amphibolite facies metamorphism. These shear zones represent a phase of movement which occurred in the 490-465 Ma interval when ambient temperatures were still high, and it is concluded that this is the principal control on the metamorphic grade achieved within the shear zones, although local anomalies may exist.

Notes: Abstract An experimental study of the system CaCO3–MgCO3–FeCO3 was undertaken in order to calibrate the iron correction to the calcite–dolomite geothermometer, which is based on the solubility of magnesium in calcite in the assemblage calcite + dolomite. The experiments, at 450°C and lower temperatures, resulted in products with a very small grain size and incomplete equilibration. However, application of a carefully-devised automatic data processing algorithm to analyses of the phases in experimental charges, combined with a thermodynamic analysis, results in geothermometer diagrams which should be preferred to previous theoretical predictions.

Notes: Abstract Biotite, garnet, staurolite and kyanite isograds in pelitic metasedimentary rocks are developed as a result of thermal metamorphism around syntectonic granitoids in Eastern Rouergue (France). Temperature estimates range between 400°C and 650°C at about 6.5 kbar. Geothermobarometry shows a steep isobaric T gradient which is consistent with the interpretation that the metamorphic highs are thermal aureoles. High grade rocks show evidence of two staurolite forming reactions in the presence of plagioclase and the absence of chlorite that have not been described previously in the literature. The reaction that occurs in the middle staurolite zone, alm-rich ga + Ca-rich pla + Na-rich mu gro-rich ga + Na-rich pla + st + Na-poor mu, is considered to be prograde, whereas the reaction that occurs in the kyanite zone, alm-rich ga + Ca-rich pla + w st + Ca-rich ga + Na-rich pla + qz, is retrograde. The topology of these reactions is illustrated in terms of end member compositions for the systems KNaFASH and KCaFASH, respectively.