Paragenetic relations in gedrite — cordierite — staurolite — biotite sillimanite — kyanite gneisses at Ajitpura,Rajasthan, India

Aluminous parageneses containing gedrite, cordierite, garnet, staurolite, biotite, sillimanite, kyanite, quartz or spinel plus corundum are found as dark colored lenses in the polymetamorphic, multideformed Archean complex at Ajitpura in northwest peninsular India. Staurolite, like kyanite, is a relict phase of earlier metamorphism and is excluded as a paragenetic mineral in view of its incompatibility with quartz and gedrite and its lower X _Mg values than for garnet of the assemblage. Its stability here is attributed to zinc content of up to 3 wt%. The XMg in other ferromagnesian minerals decreases in the order: cordierite, biotite, gedrite, garnet, as found elsewhere in high grade rocks.The textural criteria and systematic partitioning of Fe and Mg in the ferromagnesian phases, excluding staurolite, indicate attainment of equilibrium during the second metamorphism. From tie line configurations in the phase diagrams, X _Mg ratios in the constituent minerals, and other petrographic criteria, it is suggested that gedrite — cordierite-garnet — sillimanite — biotite assemblage has been produced by the reactions: Biotite+Sillimanite+Quartz = Cordierite+Garnet+K-feldspar+Vapor (1) and Biotite+Sillimanite+Quartz = Cordierite +Gedrite+K-feldspar+Vapor (2) which occurred during partial melting of the rocks at fixed P and T conditions.By isothermal P-X(Fe-Mg) sections it has been demonstrated that release of FeO, SiO₂ and other components modified the composition of the reactant biotite presumably by the substitution FeSi2 Al, whereby reaction 1 was replaced by reaction 2. Cordierite with higher X _Mg was produced with gedrite instead of with garnet, whose X _Mg is less than X _Mg of gedrite. Reaction 2 has been tentatively located in T-P space from the intersection of some continuous loops in the P-X(Fe-Mg) diagram at 700°C and also by other constraints. The discontinuous reaction 2 is located about 1–2 kilobars higher than reaction 1, which implies that it is difficult to distinguish between effects of pressure and those of melting on the X _Mg ratios of the reaction phases.The P-T calibrations of garnet — cordierite, garnet — biotite and garnet — plagioclase equilibria and the calibrations from other dehydration curves give temperatures near 700°C and pressure (assuming ) about 6 kilobars.     

Phase Equilibria of Amphibolites from the Post Pond Volcanics, Mt. Cube Quadrangle, Vermont

Amphibolites of the Post Pond Volcanics, south-west corner ofthe Mt. Cube Quadrangle, Vermont, are characterized by a greatdiversity of bulk rock types that give rise to a wide varietyof low-variance mineral assemblges. Original rock types arebelieved to have been intrusive and extrusive volcanics, hydrothermallyaltered volcanics and volcanogenic sediments with or withoutadmixtures of sedimentary detritus. Metamorphism was of staurolite-kyanitegrade. Geothermometry yields a temperature of 535 ± 20°C at pressures of 5–6 kb. Partitioning of Fe and Mg between coexisting phases is systematic,indicating a close approach to chemical equilibrium was attained.Relative enrichment of Fe/Mg is garnet > staurolite >gedrite > anthophyllite cummingtonite hornblende > biotite> chlorite > wonesite > cordierite dolomite > talc;relative enrichment in Mn/Mg is garnet > dolomite > gedrite> staurolite cummingtonite > hornblende > anthophyllite> cordierite > biotite > wonesite > chlorite >talc. between coexisting amphiboles varies as a function ofbulk Fe/Mg, which is inconsistent with an ideal molecular solutionmodel for amphiboles. Mineral assemblages are conveniently divided into carbonate+ hornblende-bearing, hornblende-bearing (carbonate-absent)and hornblende-absent. The carbonate-bearing assemblages allcontain hornblende + dolomite+ calcite + plagioclase (andesineand/or anorthite) + quartz with the additional phases garnetand epidote (in Fe-rich rocks) and chlorite ± cummingtonite(in magnesian rocks). Carbonate-bearing assemblages are restrictedto the most calcic bulk compositions. Hornblende-bearing (carbonate absent) assemblages occur in rocksof lower CaO content than the carbonate-bearing assemblages.All of these assemblages contain hornblende + andesine ±quartz + Fe-Ti oxide (rutile in magnesian rocks and ilmenitein Fe-rich rocks). In rocks of low Al content, cummingtoniteand two orthoamphiboles (gedrite and anthophyllite) are common.In addition, garnet is found in Fe-rich rocks and chlorite isfound in Mg-rich rocks. Several samples were found that containhornblende + cummingtonite + gedrite + anthophyllite ±garnet +chlorite + andesine + quartz + Fe-Ti oxide ±biotite. Aluminous assemblages contain hornblende + staurolite+ garnet ± anorthite/bytownite (coexisting with andesine)± gedrite ± biotite ± chlorite ±andesine ± quartz ± ilmenite. Hornblende-absentassemblages are restricted to Mg-rich, Ca-poor bulk compositions.These rocks contain chlorite ± cordierite ± staurolite± talc ± gedrite ± anthophyllite ±cummingtonite ± garnet ± biotite ± rutile± quartz ± andesine. The actual assemblage observeddepends strongly on Fe/Mg, Ca/Na and Al/Al + Fe + Mg. The chemistry of these rocks can be represented, to a firstapproximation, by the model system SiO₂–Al₂O₃–MgO–FeO–CaO–Na₂O–H₂O–CO₂;graphical representation is thus achieved by projection fromquartz, andesine, H₂O and CO₂ into the tetrahedron Fe–Ca–Mg–Al.The volumes defined by compositions of coexisting phases filla large portion of this tetrahedron. In general, the distributionof these phase volumes is quite regular, although in detailthere are a large number of phase volumes that overlap otherphase volumes, especially with respect to Fe/Mg ratios. Algebraicand graphical analysis of numerous different assemblages indicatethat every one of the phase volumes should shift to more magnesiancompositions with decreasing µ_H2O. It is therefore suggestedthat the overlapping phase volumes are the result of differentassemblages having crystallized in equilibrium with differentvalues of µ_H2O or µ_CO2 and that the different valuesmay have been inherited from the original H₂O and CO₂ contentof the volcanic prototype. If true, this implies that eithera fluid phase was not present during metamorphism, or that fluidflow between rocks was very restricted.     

Phase equilibria and the pressure-temperature path of the highest-grade Ryoke metamorphic rocks in the Yanai district, SW Japan

The garnet-cordierite zone, the highest-grade zone of the Ryoke metamorphic rocks in the Yanai district, SW Japan, is defined by the coexistence of garnet and cordierite in pelitic rocks. Three assemblages in this zone are studied in detail, i.e. spinel + cordierite + biotite, garnet + cordierite + biotite and garnet + biotite, all of which contain quartz, K-feldspar and plagioclase. The Mg/(Fe + Mg) in the coexisting minerals decreases in the following order: cordierite, biotite, garnet and spinel. Two facts described below are inconsistent with the paragenetic relation in the K₂OFeOMgOAl₂O₃SiO₂H₂O (KFMASH) system in terms of an isophysical variation. First, garnet and biotite in the last assemblage have Mg/(Fe + Mg) higher than those in the second. Second, the first two assemblages are described by the reaction,

Experimental study of the stability of cordierite and garnet in pelitic compositions at high pressures and temperatures

In pelitic rocks, under conditions of low f _{O 2} and low f _{H 2 O}, the stability of the mineral pair cordierite-garnet is limited by five univariant reactions. In sequence from high pressure and low temperature to high temperature and low pressure these are: cordierite+garnet hypersthene+sillimanite+quartz, cordierite+garnet hypersthene+sapphirine+quartz, cordierite+garnet hypersthene+spinel+quartz and cordierite+garnet olivine+spinel +quartz. In this sequence of reactions the Mg/Mg+Fe²⁺ ratio of all ferro-magnesian minerals involved decreases continuously from the first reaction to the fifth. The five univariant boundaries delimit a wide P-T range over which cordierite and garnet may coexist.Two divariant equilibria in which the Mg/Mg+ Fe²⁺ ratio of the coexisting phases are uniquely determined by pressure and temperature have been studied in detail. P-T-X grids for the reactions cordierite garnet+sillimanite+quartz and cordierite+hypersthene garnet+quartz are used to obtain pressure-temperature estimates for several high grade metamorphic areas. The results suggest temperatures of formation of 700–850° C and load pressures of 5–10 kb. In rare occasions temperatures of 950–1000° C appear to have been reached during granulite metamorphism.On the basis of melting experiments in pelitic compositions it is suggested that Ca-poor garnet xenocrysts found in calc-alkaline magmas derive from admixed pelitic rocks and did not equilibrate with the calc-alkaline magma.     

Cordierite-Cummingtonite Facies Rocks from the Gold Brick District, Colorado

The unusual association of cordierite and cummingtonite (? gedrite+ chlorite + biotite + ilmenite + plagioclase + quartz) definesa metamorphic facies within aluminous, low-Ca amphibolites fromthe Proterozoic rocks of the Gold Brick District, east of Gunnison,Colorado. More Fe-rich bulk chemistries in the same facies arecharacterized by assemblages consisting of cordierite+-gedrite+ garnet + chlorite + biotite + ilmenite + plagioclase + quartz,whereas more Mg-rich compositions are characterized by cordierite+ anthophyllite + chlorite + biotite + ilmenite ? plagioclase+ quartz. The assemblage gedrite 4- cummingtonite + chlorite+ biotite + ilmenite + plagioclase + quartz was also observed.Coexisting cordierite+ anthophyllite + cummingtonite was notobserved in any rocks, apparently because this assemblage isstable over only a very narrow range of bulk compositions. Metamorphosedpelitic rocks are more iron rich than the assemblage cordierite+ gedrite + garnet + chlorite + biotite + ilmenite + plagioclase+ quartz and consist of garnet ?cordierite ?staurolite ? chlorite? andalusite + biotite + ilmenite + plagioclase + quartz? microclineor muscovite. Mineral rim compositions from cordierite-bearing amphibolitesand metapelites determined by electron microprobe analysis showsystematic Fe/Mg partitioning and define assemblages that occupynon-overlapping regions of the compositional system SiO₂-TiO₂-Al₂O₃-MnO-FeO-MgO-CaO-Na₂O-K₂O-H₂Oas determined by algebraic and statistical methods developedby Braun & Stout (1975) and Fisher (1989). Graphical methods(projections) produced spurious overlaps not confirmed by themore rigorous algebraic tests. The spurious overlaps were generatedbecause standard projective analysis was not able simultaneouslyto account for the important effects of the components Na₂O,CaO, and MnO on the AFM topologies. The results of algebraicand statistical analysis are consistent with an equilibriumorigin at constant values of temperature and pressure. The cordierite-cummingtonite facies encompasses the relativelylow-pressure and moderate-temperature conditions associatedwith the stability field of andalusite. Garnet-biotite geothermo-metry,and garnet, aluminosilicate, silica, plagioclase (GASP) geobarometrysuggest that temperatures and pressures were nearly constantacross the study area at 550( ? 70) ?C and 3 kb, respectively,near the peak of metamorphism. Other geothermometers and geobarometers,and independent pressure and temperature estimates, are compatiblewith garnet-biotite thermometry and GASP geo-barometry. Gradientsin fO₂ or H₂O are not required to explain the compatibilityof these assemblages at constant T and P. Cordierite + cummingtonite-bearingrocks can apparently be derived from anthophyllite +garnet-bearingrocks by increasing temperature or decreasing pressure.     

Kornerupine in Mg-Al-rich gneisses from Namaqualand,South Africa: mineralogy and evidence for late-metamorphic fluid activity

Three kornerupine occurrences are reported in distinctive SiO₂-poor, MgO- and Al₂O₃-rich paragneisses from the Namaqualand Metamorphic Complex in South Africa. Kornerupine coexists stably with phlogopite, cordierite, orthopyroxene, gedrite, sapphirine, sillimanite and plagioclase and, in sapphirine-free rocks, with spinel and corundum. Tourmaline of a texturally older generation than kornerupine is commonly present in the same samples.Ten analysed kornerupines show a variation in total Fe as FeO from 1.8 to 10.9 weight per cent. B₂O₃ contents are estimated from x-ray data and a few spectrochemical analyses to range from 0.9 to 3.5 weight per cent. There is a strong inverse correlation between B³⁺ and Al³⁺. Total iron content has a strong and systematic effect on refractive index, colour and dispersion. Fe and Mg are systematically partitioned with the other minerals, and Mg/(Mg+Fe) ratios increase as follows: spinel 相似文献   

A field and theoretical analysis of garnet+chlorite+chloritoid+biotite assemblages from the tri-state (MA,CT, NY) area,USA

The prograde evolution of minerals in metapelites of a Barrovian sequence from the tri-state area (Massachusetts, Connecticut, New York) of the Taconic Range involves assemblages with garnet (Ga), chlorite (Ch), chloritoid (Ct), biotite (Bi) and staurolite (St). Detailed petrologic observations, mineral compositions and chemical zoning in garnet show: (1) garnet high in Mn and Fe but low in Mg is stable with chlorite at grades below those where chloritoid+biotite is found; (2) early formed garnet reacted partially to form Ct+Bi at intermediate grades; (3) at higher grades garnet (with low Mn)+chlorite is again produced, at the expense of chloritoid+biotite, suggesting a reversal in the continuous reaction involving the phases Ga, Ch, Ct and Bi. Thermodynamic modeling of the assemblage Ga+Ch+Ct+Bi±St in the MnKFMASH system reveals: (1) in the MnKFASH system the prograde reaction is Ga+Ch=Ct+Bi whereas in the KFMASH system the prograde reaction is the opposite: Ct+Bi=Ga+Ch; (2) the Ga–Ch–Ct–Bi–St invariant point in the KFMASH system occurs twice, at approximately 6.5 kbar, 545° C and 14.8 kbar, 580° C (although one of them may be metastable in a complex phase system); the appearance of the petrogenetic grid is markedly different from that of Albee, but similar to that of Spear and Cheney; (3) as a consequence, in the KFMASH system, chloritoid+biotite are stable over a wide range of P-T conditions whereas garnet+chlorite assemblages are restricted to a narrow band of P-T conditions; (4) MnO increases the stability field of Ga+Ch relative to both Ct+Bi at low temperatures, and St+Bi at high temperatures; (5) in natural samples the occurrence of Ct+Bi is controlled more by bulk Mg–Fe(-Mn) composition than P-T conditions. Specifically, Ct+Bi is restricted to bulk compositions with Fe/(Mg+Fe+Mn)>0.6. Rocks with Fe/(Mg+Fe+Mn)<0.5 are likely to display only chlorite+biotite at low grade. These observations are consistent with Wang and Spear and Spear and Cheney.     

Garnet in silicic liquids and its possible use as a P-T indicator

Melting experiments on a model pelitic composition yield low-spessartine garnet as an important residual phase at pressures above 7 kb. The K _D values for distribution of iron and magnesium between coexisting garnet and liquid in the pelitic composition are mainly sensitive to temperature, but also have a small pressure dependence. At temperatures above 950 ° C garnet has a higher value than coexisting liquid, but below 950 ° C the garnet value is lower than that of the coexisting liquid. Thus at temperatures below 950 ° C silicic magmas may fractionate garnet and produce more magnesian derivative liquids.Reconnaissance experiments with added MnO content in the model pelite demonstrate that spessartine-rich garnets are stable in silicic liquids to pressures as low as 3 kb. The MnO and CaO contents of the experimentally crystallized garnets show an antipathetic relation. Also, the grossular content of near-liquidus garnets crystallizing from a range of compositions increases with increasing pressure. The spessartine and grossular contents of most natural garnets in eastern Australian granitic rocks suggest that these garnets formed at pressures greater than 5 kb. Increased spessartine content allows crystallization of garnet in equilibrium with a silicic magma well within the pressure limit of stability of cordierite, provided the garnet contains 10 mol.% spessartine. Thus the depth range over which garnet and cordierite may coexist in a silicic melt is broadened, subject to the availability of MnO. The effect of increased Mn content on the low-pressure stability limit of garnet may also explain the lack of resorption of some garnets in granitic magmas, as these magmas rise to shallower levels. These euhedral garnets characteristically show zoning from an Mn-poor core (typically <4 % MnO) to an Mn-richer rim (typically >4 % MnO) and may reflect continued growth of the garnet in a low pressure regime, stabilized by Mn concentrated in the residual liquid fractions of the crystallizing magma.     

The variation in garnet,biotite and chlorite composition in medium grade pelitic rocks from the Dalradian,Scotland, with particular reference to the zonation in garnet

Garnet, biotite and host rock have been analysed along a traverse from the garnet isograd to the kyanite zone in the Dalradian of Central Perthshire, Scotland. FeO and MgO increase and MnO and CaO decrease in the garnet with increasing grade. Microprobe analyses of the garnets reveal zoning, which indicates that a garnet crystal as a whole does not equilibrate with the matrix during growth. Coexisting biotite varies in composition as a result of the abstraction of MnO, FeO etc. from the rook by the growing garnet, i.e. the mg/mg + fe ratio increases with grade. The microprobe analyses also reveal the size of the system from which garnet abstracted material varied from 0.100 to 2.000 g and the nucleation was frequently instantaneous. It also reveals the equilibrium or non-equilibrium nature of the assemblage, and explains the variation in garnet composition with grade in terms of a segregation model with a changing distribution coefficient. Primary chlorite was analysed from rocks near to the garnet isograd containing garnet and biotite. It has a similar mg/mg + fe value to the coexisting biotite. The results show that the three phase field defining the garnet isograd moves towards the mg corner with increasing grade. The higher grade fields lie to the mg rich side of the three phase field so that the sequence of mineral assemblages across the Barrovian zones in Perthshire, from the garnet isograd to the kyanite zone, can be summarized and displayed on a phase diagram.     

The assemblage quartz — Sillimanite — Garnet — Cordierite as an indicator of metamorphic conditions in the Daly Bay Complex,N.W.T.

If cordierite is treated as an anhydrous mineral, the composition of garnet and cordierite, coexisting with quartz and silliminate, depends on total pressure and temperature. Phase relations may be deduced by combining some available experimental work with several approximations. Assuming ideal ionic solution in garnet and cordierite, analyses of coexisting garnet and cordierite permit the determination of total pressure and temperature. Five rocks from the Daly Bay Complex, N. W. T., collected from locations up to 35 miles apart, indicate a range of 610–760 and 5.3–6.6 kb.     

Osumilite-sapphirine-quartz granulites from Enderby Land Antarctica — Mineral assemblages and reactions

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 OsCd+En+Kfeld+Qtz, OsSa+En+Kfeld+Qtz, OsSill+En+Kfeld+Qtz. In iron-bearing systems an important reaction involving osumilite is Os+GtCd+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.Published with the permission of the Director, Bureau of Mineral Resources     

Iron- and manganese-rich minor intrusions emplaced under late-orogenic conditions in the proterozoic of South Greenland

Three small intrusions in Ketilidian gneisses near Julianehaab comprise sheets and veins of olivine-magnetite-grunerite or magnetite-amphibole rocks partly surrounded by garnetiferous hornblende-biotite granitoid rock. The latter skin locally widens out into diffuse bodies of fayalite-orthopyroxene-quartz syenite or monzonite and biotite granite, which show layering similar to that resulting from gravity settling of crystals. Near the intrusions the country rocks lose their foliation and have been partially melted. Intrusion probably occurred at the close of regional metamorphism 1,750–1,780 m.y. ago, just prior to emplacement of the rapakivi granite suite of South Greenland. The mafic minerals of the intrusions are markedly enriched in iron and, in the case of olivine, orthopyroxene, grunerite and garnet, in manganese as well: olivine Fa₉₀Te₅Fo₅; orthopyroxene (inverted pigeonite) Ca₂Fe₇₇Mn₆Mg₁₅; calciferous amphiboles are typically hastingsitic; biotites generally have Fe/Fe+Mg ratios of 0.8; garnets are almandine-grossularite-spessartine mixtures; essentially pure magnetite is the dominant oxide mineral and ilmenite is only moderately manganiferous. Crystallization of the mafic rocks appears to have followed the trend of the quartz-fayalite-magnetite buffer curve from perhaps 800°C to <550°C at pressures, calculated from thermodynamic considerations, of 4 to 5 kb. However, the presence of Mn makes estimates of pressure and temperature uncertain. Comparison with other late- to post-orogenic intrusions—the South Greenland and Finnish rapakivi granite suites, the Labrador adamellite complex and the Pikes Peak batholith of Colorado—reveals both similarities and differences, particularly with respect to mineral parageneses, depth of emplacement and manganese enrichment.     

Petrogenesis of cordierite-orthoamphibole assemblages from the Springton region,South Australia

Textural evidence for the partial breakdown of staurolite-biotite and andalusite-biotite assemblages to cordierite-orthoamphibole implies high temperature metasomatic depletion of K₂O in semi-pelitic rocks from Springton, South Australia. The origin of the reaction textures is discussed with reference to K₂O-T diagrams derived from the topologically equivalent K₂O–(-H₂O) diagram showing both discontinuous and Fe–Mg continuous reactions. The involvement of fluids in the metasomatic process is implied by the scale of K₂O removal and suggests that the outcrop pattern of cordierite-gedrite rocks reflects, at least in part, a heterogeneous distribution of advecting fluids in the metamorphic pile at high temperatures.Mineral abbreviations used in text and figures ab albite - alm almandine - als aluminosilicate - and andalusite - anth anthophyllite - bt biotite - cd cordierite - fe-bt Fe-rich biotite - fe-cd Fe-rich cordierite - fe-oa Fe-rich orthoamphibole - fe-st Fe-staurolite - gt garnet - ksp potassium feldspar - ky kyanite - mg-cd Mg-rich cordierite - mg-oa Mg-rich orthoamphibole - mg-st Mg-rich staurolite - mu muscovite - oa orthoamphibole - phl phlogopite - plag plagioclase - py pyrope - sill sillimanite - st staurolite - v vapour     

Ca distribution between almandine-rich garnet and plagioclase in pelitic and psammitic schists from the metamorphic basement of North-Eastern Sardinia

Garnet and plagioclase pairs from fourteen selected samples, from garnet to sillimanite zones, collected along a NS traverse throughout the metamorphic basement of NE Sardinia, have been analyzed by microprobe.Beyond the garnet isograd, plagioclase has albitic composition and the garnet (a Ca-rich almandine) shows Ca/ Ca+Mg+Fe ratios of about 0.35–0.30, fairly constant from core to rim.Towards the North, still in the garnet zone, when on the large albitic core of plagioclase a thin and discontinuous oligoclasic rim (An₂₂–An₁₈) formed, we observe in the garnet edge an abrupt decrease of the Ca/Ca+Mg+Fe ratio (0.27–0.16).In the staurolite and sillimanite zones garnet does not show significant Ca-zoning and it is characterized by low Ca content (Ca/Ca+Mg+Fe<0.1); the coexisting plagioclase has oligoclasic (An₁₆–An₂₇) composition.The chemical data and the microstructural evidence on growth time indicate that the garnet and plagioclase had a strong mutual interference in determining the relative Ca distribution.The most relevant reactions are discussed and, in particular, the antipathetical Ca-zoning, recorded by garnet and plagioclase in the garnet zone, is considered as the evidence of temperature increase during growth of the two minerals. It is also suggested that the sharp variation of Ca content at the garnet edge was controlled by the discontinuous nature of plagioclase solid solution in the peristeritic range.The order of appearance of garnet and oligoclase in the basement of NE Sardinia is also discussed in comparison with other well known metamorphic sequence (Vermont, New Zealand and Dalradian). It is concluded that the different order of appearance is controlled other than the different nature of the calcic phases in the lower grade zones also by the in the fluid phase.     

Recalibration of mutually consistent garnet–biotite and garnet–cordierite geothermometers

Garnet–biotite and garnet–cordierite geothermometers have been consistently calibrated, using the results of Fe²⁺–Mg cation exchange experiments and utilizing recently evaluated nonideal mixing properties of garnet. Nonideal mixing parameters of biotite (including Fe, Mg, Al^VI, and Ti) and of cordierite (involving Fe and Mg) are evaluated in terms of iterative multiple least-square regressions of the experimental results. Assuming the presence of ferric Fe in biotite in relation to the coexisting Fe-oxide phases (Case A), and assuming the absence of ferric Fe in biotite (Case B), two formulae of garnet–biotite thermometer have been derived. The garnet–cordierite geothermometer was constructed using Margules parameters of garnet adopted in the garnet–biotite geothermometers. The newly calibrated garnet–biotite and garnet–cordierite thermometers clearly show improved conformity in the calculated temperatures. The thermometers give temperatures that are consistent with each other using natural garnet–biotite–cordierite assemblages within ±50 °C. The effects of ferric Fe in biotite on garnet–biotite thermometry have been evaluated comparing the two calibrations of the thermometer. The effects are significant; it is clarified that taking ferric Fe content in biotite into account leads to less dispersion of thermometric results.     

Experimental calibration of the partitioning of Fe and Mg between biotite and garnet

The cation exchange reaction Fe₃Al₂Si₃O₁₂ +KMg₃AlSi₃O₁₀(OH)₂ = Mg₃Al₂Si₃O₁₂+KFe₃-AlSi₃ O₁₀(OH)₂ has been investigated by determining the partitioning of Fe and Mg between synthetic garnet, (Fe, Mg)₃Al₂Si₃O₁₂, and synthetic biotite, K(Fe, Mg)₃AlSi₃O₁₀(OH)₂. Experimental results at 2.07 kbar and 550 °–800 ° C are consistent with In [(Mg/Fe) garnet/(Mg/Fe) biotite] = -2109/T(°K) +0.782. The preferred estimates for ¯H and ¯S of the exchange reaction are 12,454 cal and 4.662 e.u., respectively. Mixtures of garnet and biotite in which the ratio garnet/biotite=49/1 were used in the cation exchange experiments. Consequently the composition of garnet-biotite pairs could approach equilibrium values in the experiments with minimal change in garnet composition (few tenths of a mole percent). Equilibrium was demonstrated at each temperature by reversal of the exchange reaction. Numerical analysis of the experimental data yields a geothermometer for rocks containing biotite and garnet that are close to binary Fe-Mg compounds.     

Experimental study of the stability of cordierite and garnet in pelitic compositions at high pressures and temperatures

The stability of cordierite and garnet relative to their anhydrous breakdown products, i.e. hypersthene, sapphirine, olivine, spinel, sillimanite and quartz, has been studied experimentally in model pelitic compositions (system MgO-FeO-Al₂O₃-CaO-K₂O-SiO₂). Below 1000° C cordierite breaks down according to the divariant reaction cordierite garnet+sillimanite+quartz (1) for most values of the MgO/MgO + FeO ratio (X). At very high values of X (ca. X0.9) garnet in reaction (1) is replaced by hypersthene. The position and width of the divariant field (in terms of pressure and temperature) in which cordierite and garnet coexist, is a function of the MgO/MgO + FeO ratio. If this ratio is increased then the stability field of garnet is reduced and that of cordierite extended towards higher pressure. Compositions of coexisting cordierite and garnet in divariant equilibrium have been analysed by electron probe micro-analyser. These compositions are unique functions of pressure and temperature. Above ca. 1000° C the breakdown of cordierite involves the phases sapphirine and hercynite-rich spinel in Mg-rich and Fe-rich compositions respectively.     

Sapphirine bearing granulites from the Sipiwesk Lake area of the late Archean Pikwitonei granulite terrain,Manitoba, Canada

Sapphirine occurs in the orthopyroxene-cordierite and feldspar-sillimanite granulites in the Sipiwesk Lake area of the Pikwitonei granulite terrain, Manitoba (97°40W, 55°05N). The orthopyroxene-cordierite granulites have extremely high Al₂O₃ (24.5 wt%) and MgO (24.6 wt%) contents and contain sapphirine (up to 69.2 wt% Al₂O₃), aluminous orthopyroxene (up to 8.93 wt% Al₂O₃), cordierite, spinel, phlogopite, and corundum. Sapphirine forms coronas mantling spinel and corundum. Corona sapphirine is zoned and its composition varies through the substitution (Mg, Fe, Mn) Si=2 Al as a function of the phases with which it is in contact. Textural and chemical relationships of sapphirine with coexisting phases indicate that spinel + cordierite reacted to form orthopyroxene + sapphirine under conditions of increasing pressure. Moreover, decreasing core to rim variation of Al₂O₃ in orthopyroxene porphyroblasts suggests decreasing temperature during sapphirine formation. On the basis of experimentally determined P-T stability of the assemblage enstatite + sapphirine + cordierite, and the Al content of hypothetical Fe²⁺-free orthopyroxene associated with sapphirine and cordierite, metamorphic temperatures and pressures are estimated to be 860–890° C and 3.0–11.2 kbar.In the feldspar-sillimanite granulites, sapphirine occurs as a relict phase mantled by sillimanite and/or by successive coronas of sillimanite and garnet. These textural relations suggest the reaction sapphirine + garnet + quartz = orthopyroxene + sillimanite with decreasing temperature. Compositions of minerals in the assemblage garnet-orthopyroxene-sillimanite-plagioclase-quartz, indicate metamorphic P-T conditions of 780–880° C and 9±1 kb.The metamorphic conditions estimated in this study suggest that the sapphirine bearing granulites in the Sipiwesk Lake area represent Archean lower crustal rocks. Their formation might be related to the crustal thickening processes in this area as suggested by Hubregtse (1980) and Weber (1983).     

Chemistry, reaction mechanisms and micro-structures during retrograde metamorphism of gedrite-biotite-plagioclase bearing rocks from Bergslagen, south-central Sweden

The Proterozoic rhyolitic volcanics constituting the foot-wall rocks in the Stollberg ore-field, Bergslagen, south-central Sweden, locally contain gedrite altered to chlorite and serpentine, biotite altered to chlorite and plagioclase altered to epidote.

The intergrowths between the host gedrite and the chlorite/serpentine inclusions are oriented with the a^* of gedrite parallel to the c^* of serpentine and chlorite. The biotite has been altered to chlorite by brucitization of both the K-interlayer and talc-like layer. In both cases the net change in volume during chloritization is small.

The assumption that Al is conserved during alteration of gedrite and biotite agrees very well with the micro-structures and orientation relations observed by transmission electron microscopy. Normalizing the chlorite to 1.00 mole, the overall chemical change that took place during the retrograde metamorphism of the Stollberg rocks can be written as: 0.84Ged+0.14Bio+0.65Mg+4.76H₂O+0.42H=1.00Chl+0.57Alb+0.72Fe+0.01Na+0.12K+0.01Ti+0.05Mn+0.95H₄SiO₄ The reaction results in ca 9% increase in volume for the solid phases. Thus, a slightly acidic Mg-rich fluid started the reaction and, upon leaving the system, the metasomatic fluid was enriched in Na, Fe, K, and Si.     

A garnet-cordierite granite porphyry containing rapakivi feldspars in the Cabeza de Araya batholith (extremadura,spanish Hercynian belt)

Summary The garnet-cordierite granite porphyry is a large dyke associated with the Cabeza Araya batholith. The batholith shows S typology but with intermediate characteristics between the aluminous granite series, spatially and genetically related to the Hercynian regional metamorphism, and the calc-alkaline series of the Iberian massif. The granite porphyry is rich in megacrystic alkali feldspar often with rapakivi texture. Its mineralogy consists mainly of quartz + plagioclase + alkali feldspar + biotite I + cordierite I + garnet + biotite 11 + cordierite II ± muscovite + chlorite.Cordierite-garnet thermobarometry and stability relationships of ternary feldspars are used to estimate the T-P conditions of crystallization and the evolution of these rocks. The equilibrium temperature obtained from the cordierite-garnet pair is about 800°C (4 ± 0.5 Kb). This shows the xenocrystic origin of cordierite and garnet, in accordance with other geological and textural evidence. Garnet transformation, the genesis of Cordierite II and the formation of mantled textures are interpreted as the result of an isothermal decompression accompanying the emplacement of the porphyry.

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Eine Rapakivi-Feldspat führender Granat-Codierit-Granitporphyr aus dem Cabeza de Araya Batholith (Extremadura, Hereynischer Gürtel, Spanien)

Zusammenfassung Der Granat-Cordierit-Granit stellt einen mit dem Cabeza Araya Batholith assoziierten, mächtigen Gang dar. Der Batholith zeigt S-Typ Charakter, jedoch mit bergangsmerkmalen zu aluminösen Granitserien, und steht räumlich und genetisch im Zusammenhang mit der hercynischen Regionalmetamorphose und den Kalkalkaliserien des iberischen Massivs. Der Granitporphyr führt häufig Megakristalle von Alkalifeldspat, die oft Rapakivitextur zeigen. Die Mineralogie des Granitporphyr besteht aus Quarz + Plagioklas + Alkalifeldspat + Biotit 1 + Cordierit 1 + Granat + Biotit II + Cordierit II ± Muscovit ± Chlorit. Die P-T Bedingungen der Kristallisation und die magmatische Entwicklung dieserDie wurde, P-T Bedingungen der Kristallisation und die magmatische Entwicklung dieser Gesteine wurde, unter Anwendung der Cordierit-Granat Thermobarometrie und den Stabilitätsbeziehungen der Feldspäte, ermittelt. Die Gleichgewichtstemperatur aus Cordierit-Granat-Paaren beträgt um 800°C (4 ± 0.5 Kb). Dies zeigt die Bildung von Cordierit und Granat als Xenokristalle, in Übereinstimmung mit anderen geologischen und texturellen Merkmalen. Die Transformation des Granat. die Genese von Cordierit II und das Entstehen von mantled Texturen, kann als Resultat einer isothermalen Dekompression interpretiert werden, die die Platznahme des Porphyrs begleitet hat.

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With 5 Figures