ALBERT

Notes: Regionally metamorphosed metapelites from Rogaland, SW Norway, contain zircon formed during the decompression reaction garnet + sillimanite + quartz → cordierite. The zircon, which occurs as inclusions in cordierite coronas around garnet, is texturally, chemically and isotopically distinct from older zircon in other textural settings in the matrix. A SHRIMP U–Pb age of 955 ± 8 Ma based on analyses in thin section on the decompression zircon from the cordierite coronas, therefore dates a point on the retrograde path, estimated from garnet–cordierite equilibria to be 5.6 kbar, 710 °C. This population was under-represented in conventional SHRIMP analyses of individual zircon in a mono-mineralic grain mount and, in the absence of a textural context, its significance unknown. The dominant age identified from SHRIMP analyses of the grain mount, in combination with analyses from matrix zircon in thin section, was 1035 ± 9 Ma. Based on the lack of consistent textural relationships with any specific minerals in thin section, as well as rare earth element chemistry, the 1035-Ma population is interpreted to represent zircon growth during incipient migmatization of the rocks at 6–8 kbar and c. 700 °C. This is consistent with previous estimates for the age of regional M1 metamorphism during the Sveconorwegian Orogeny. The most important outcome of this study is the successful analysis of zircon grains in a specific, well-constrained reaction texture. Not only does this allow a precise point on the regional P–T path to be dated, but it also emphasizes the possibility of zircon formation during the retrograde component of a typical metamorphic cycle.

Notes: Geochronological data, combined with field and petrological evidence, constrain the timing and rate of near-isothermal decompression at granulite facies temperatures in rocks from the Lützow-Holm Complex of East Antarctica. Granulite facies gneisses from Rundvågshetta in Lützow-Holm Bay experienced a peak metamorphic temperature of over 900 °C at c. 11 kbar, as evidenced by primary orthopyroxene–sillimanite-bearing assemblages, and secondary cordierite–sapphirine-bearing assemblages in metapelites. Peak metamorphic assemblages show strong preferred mineral orientation, interpreted to have developed synchronously with pervasive ductile deformation. Zircon from a syndeformational leucosome has a U–Pb age of 517±9 Ma, which is interpreted as a melt crystallization age. This age provides the best estimate of the time of peak metamorphic conditions. The post-peak metamorphic history is characterized by near-isothermal decompression, recorded by mineral textures in a variety of rock compositions. Field and textural relations indicate that decompression post-dated pervasive ductile deformation. K/Ar and 40Ar/39Ar ages from hornblende and biotite represent closure ages during cooling subsequent to decompression, and indicate cooling to temperatures between c. 350 and 300 °C by c. 500 Ma, thus placing a lower time limit on the duration of the high-temperature isothermal decompression episode. The combination of the zircon age from a syndeformational melt with K/Ar and 40Ar/39Ar closure ages indicates that near-isothermal decompression from c. 11 to c. 4 kbar at granulite facies temperatures, followed by cooling to c. 300 °C, took place within a time interval of 20±10 Myr. Simple one-dimensional models for exhumation-controlled cooling indicate that these data require exhumation rates of the order of c. 3 km Myr−1 for several million years, then cessation of exhumation followed by relatively isobaric cooling during thermal re-equilibration.

Notes: The solid-state reaction magnesite (MgCO3) + calcite (aragonite) (CaCO3) = dolomite (CaMg(CO3)2) has been identified in metapelites from western Tianshan, China. Petrological studies show that two metamorphic stages are recorded in the metapelites: (1) the peak mineral assemblage of magnesite and calcite pseudomorphs after aragonite which is only preserved as inclusions within dolomite; and (2) the retrograde glaucophane-chloritoid facies mineral assemblage of glaucophane, chloritoid, dolomite, garnet, paragonite, chlorite and quartz. The peak metamorphic temperatures and pressures are calculated to be 560–600 °C, 4.95–5.07 GPa based on the calcite–dolomite geothermometer and the equilibrium calculation of the reaction dolomite = magnesite + aragonite, respectively. These give direct evidence in UHP metamorphic rocks from Tianshan, China, that carbonate sediments were subducted to greater than 150 km depth. This UHP metamorphism represents a geotherm lower than any previously estimated for subduction metamorphism (〈 3.7 °C km−1) and is within what was previously considered a ‘forbidden’ condition within Earth. In terms of the carbon cycle, this demonstrates that carbonate sediments can be subducted to at least 150 km depth without releasing significant CO2 to the overlying mantle wedge.

Notes: Abstract The pre-Cambrian granulites of Enderby Land Antarctica, contain coexisting spinel-quartz, sapphirine-quartz, hypersthene-sillimanite-quartz and osumilite on a regional extent. Osumilite is present in a variety of mineral assemblages, most of which are documented in granulites for the first time. The mineral assemblages, reactions and compositional zoning in minerals are discussed in terms of continuous and discontinuous reactions in response to changing conditions of metamorphism. The development of many of the mineral coronas can be explained by continuous rather than discontinuous reactions, due to the effects of Mg-Fe and (Mg,Fe)-2Al exchange equilibria with decreasing temperature. The highest P-T conditions of metamorphism (8–10 kb, 900 °–980 ° C, Ellis, in preparation) were beyond the stability limit of coexisting garnet-cordierite. Secondary cordierite has developed through a large number of mineral reactions in response to cooling of these granulites. A theoretical analysis of the phase relations involving osumilite in the chemical systems K2O-MgO-Al2O3-SiO2 and K2O-MgO-FeO-Al2O3-SiO2 is presented. In the pure Mg-system the lower temperature stability limit of Mg-osumilite is inferred to be defined with increasing pressure by the reactions Os→Cd+En+Kfeld+Qtz, Os→Sa+En+Kfeld+Qtz, Os→Sill+En+Kfeld+Qtz. In iron-bearing systems an important reaction involving osumilite is Os+Gt→Cd+Hy+Kfeld+Qtz. At moderate temperatures and pressures, osumilite is limited to rocks which lie on the Mg-rich side of the Cd-Hy stable tie line on an AFM diagram. At higher pressures and temperatures osumilite occurs in a widerrange of rock compositions because of the stability of coexisting garnet and osumilite. Petrographic data, as well as chemographic relations indicate that for many common rock compositions, garnet, cordierite, hypersthene, sapphirine and sillimanite cannot coexist with both osumilite and K-feldspar.

Notes: Abstract Osumilite-sapphirine-quartz granulites from Enderby Land, Antarctica (Ellis et al. 1980) were metamorphosed at 8–10 kb pressure, 900°-980° C under very low $$P_{H_2 O} $$ conditions. Retrograde mineral coronas in these rocks record subsequent cooling from the peak of metamorphism at approximately constant pressure. The inferredP-T cooling-uplift path differs markedly from that evident in many other granulite terrains. Present garnet-cordierite geothermometers imply equilibration at temperatures of 500°–600° C, well within the kyanite stability field. These temperatures are inconsistent with the presence of sillimanite and the high temperature stability fields of the actual mineral assemblages. Examination of available garnetcordierite experimental data suggests a possible large increase in the Gt-Cd Fe-MgK D with increasingX Mg of the cordierite (and pressure). New experiments designed to test this possibility were inconclusive because of the failure to attain satisfactory equilibrium, even at 1,000° C. Possible reasons for the exposure of these unusual granulites in Enderby Land are considered. Although they formed at much higher temperatures than other granulites exposed on a regional scale, suchP-T conditions are not exceptional for the base of the crust. Instead, the unusual isobaric cooling to low temperatures followed by uplift to the surface which these granulites are inferred to have undergone is considered of importance. The unusual tectonic conditions are reflected in the disctinctive type of mineral reaction coronas found in these rocks. The common occurrence elsewhere of mineral reaction during uplift, and the role of anatexis during uplift in obliterating such high temperature assemblages elsewhere in the world are considered.

Notes: Abstract A series of basaltic compositions and compositions within the simple system CaO-MgO-FeO-Al2O3-SiO2 have been crystallized to garnetclinopyroxene bearing mineral assemblages in the range 24–30 kb pressure, 750°–1,300° C temperature. Microprobe analyses of coexisting garnet and clinopyroxene show that K D(Fe2+/MgG+/Fe2+/MgCpx) for the Fe-Mg exchange reaction between coexisting garnet and clinopyroxene is obviously dependent upon the Ca-content and apparently independent of the Mg/(Mg+Fe) content of the clinopyroxene and garnet. The Ca-effect is believed to be due to a combination of non-ideal Ca-Mg substitutions in the garnet and clinopyroxene. Our data and interpretation reconciles previous inconsistencies in the temperature dependence of K D − values determined in experimental studies of simple systems, complex basalt, grospydite and garnet peridotite compositions. Previous differences between the effect of pressure upon K Das predicted from simple system theory (Banno, 1970), and that observed in experiments on multicomponent natural rock compositions (Råheim and Green, 1974a) can now be resolved. We have determined K Das a function of P, T, and X Gt Ca (grossular) and derived the empirical relation $$T\left( {^\circ {\text{K}}} \right) = \frac{{3104X_{{\text{Ca}}}^{{\text{Gt}}} + 3030 + 10.86P\left( {{\text{kb}}} \right)}}{{\ln K_{\text{D}} + 1.9034}}$$ . This empirical relationship has been applied to garnet-clinopyroxene bearing rocks from a wide range of geological environments. The geothermometer yields similar estimates for garnet-clinopyroxene equilibration for neighbouring rocks of different composition and different K Dvalues. In addition, temperature estimates using the above relationship are more consistent with independent temperature estimates based on other geothermometers than previous estimates which did not correct for the Ca-effect. An alternative approach to the above empirical geothermometer was attempted using regular solution models to derive Margules parameters for various solid solutions in garnets and clinopyroxenes. The derived Margules parameters are broadly consistent with those determined from binary solution studies, but caution must be exercised in interpreting them in terms of actual thermodynamic properties of the relevant crystalline solid solutions because of the assumptions which necessarily have to be made in this approach.

Notes: Abstract We report here that some of the pelitic rocks from the Wanni and Highland Complexes of Sri Lanka reacted with CO2-rich fluids to produce a wide range of unusual secondary carbonate-silicate-oxide-sulphide assemblages. These enable the depth, temperature and fluid compositions of CO2 reactions to be calculated more rigorously than is generally possible for the patches of arrested charnockite that have been described from Sri Lanka. Magnesite-andalusite-quartz has partially replaced primary cordierite, and siderite-rutile replaced ilmenite. Paragenetic sequences involving primary pyrrhotite, ilmenite and magnetite and secondary pyrite-siderite-rutile-magnetite-(hematite) demonstrate the control which carbonate equilibria have upon evolving fluid compositions during cooling. Direct evidence for the role of graphite as a source of CO2 is found in the Highland Complex where primary graphite partially reacted with silicates to form secondary siderite assemblages. It is proposed that following peak metamorphism, continued uplift along a clockwise P-T-t path was accompanied by a series of devolatilization reactions involving breakdown of graphite and the continuous production of secondary CO2-rich fluids. The limited extent of disseminated secondary carbonate reflects the small amount of graphite inferred to have been present in the source rocks. These rocks demonstrate that CO2-rich fluids, as found in disseminated fluid inclusions, need not form during peak granulite metamorphism but may be an inevitable consequence of continued uplift along a clockwise P-T-t path. The arrested charnockite which overprinted some of the hornblende-bearing felsic-intermediate composition rocks in Sri Lanka most likely formed by the same process.

Notes: Abstract High pressure pyroxene- and amphibole-rich inclusions are found in a number of Victorian Newer Volcanics volcanoes. The host lavas range from nepheline basanite to nepheline hawaiite and nepheline mugearite. The wide variation in chemistry and mineralogy of the inclusions is explained by crystallization from basaltic magmas under varying P-T and PH2O conditions at depth. At moderate pressure wehrlite inclusions (ol+cpx) form, whereas at higher pressures pyroxenites (opx+cpx) and genetically related megacrysts form. Under relatively anhydrous conditions the clinopyroxene megacrysts show a trend of Ca enrichment whereas under hydrous conditions, when amphibole is also stable, the pyroxene shows a trend to greater iron enrichment. The trend nepheline basanite to nepheline mugearite has developed by extensive fractionation of amphibole at elevated pressures under hydrous conditions. Under less hydrous conditions where clinopyroxene assumes the dominant role during crystal fractionation, derivative liquids display a trend of increasing K2O/Na2O ratio, with little modification of their level of undersaturation. Olivine plays a decreasing role in crystal fractionation processes with increasing pressure. The available evidence indicates that the only magma which could have been parental to the observed basanites was a more picritic basanite.