Mineralogy of New Caledonian metamorphic rocks

The chemistry and phase relations of calcic and sodic amphiboles in the Ouégoa blueschists are investigated. The first appearance of sodic amphiboles is controlled by bulkrock chemistry. Sodic amphibole appears first in weakly-metamorphosed pumpellyite metabasalts prior to the crystallization of lawsonite but does not crystallize in pelitic schists until the middle of the lawsonite zone; sodic amphibole continues as an apparently stable phase in rocks of all bulk compositions into, and throughout, the highest-grade rocks in the district. Calcic amphibole is widespread in metabasalts of the lawsonite and epidote zones and also occurs in metasediments of appropriate composition. Coexisting pairs of calcic and sodic amphiboles are common in metabasalts but they have also been found in some metasediments. A grunerite-riebeckite pair is described.Electron-probe analyses of 120 amphiboles from representative rock-types are presented in graphical form. Sodic amphiboles show an increased Mg/(Mg+Fe) ratio with increasing metamorphic grade. Sodic amphiboles in pelitic schists are ferroglaucophane in the lawsonite zone and crossite and glaucophane in the epidote zone. Sodic amphiboles in metabasalts are iron-rich crossites in weakly-metamorphosed rocks and more-magnesian crossites and glaucophanes in the lawsonite and epidote zones. The abrupt increase in Mg/(Mg+Fe) ratio in sodic amphiboles at the epidote isograd is attributed to the crystallization of epidote and almandine which take the place of lawsonite and spessartine of the lawsonite zone. Calcic amphiboles are fibrous actinolites in the lawsonite zone and grade with increasing Al and Na/Ca ratio into prismatic blue-green hornblendes (barroisites) in the upper epidote zone. In calcic amphiboles, increasing metamorphic grade effects the coupled substitution of (Na+Al) for (Ca+Mg) and a small increases in Fe/Mg ratio; octahedrally and tetrahedrally coordinated Al increases in an approximately 11 ratio. Both the calcic and the sodic amphiboles show an increase in A-site occupancy with increasing metamorphic grade. In two-amphibole assemblages Ti, Mn and K are concentrated in the calcic amphibole.The textural and chemical relations between coexisting calcic and sodic amphiboles are discussed. If the calcic and sodic amphiboles are an equilibrium pair then the data collected from the Ouégoa amphiboles gives a picture of a very asymmetric solvus in the system glaucophane-actinolite-hornblende, i.e. steep-sided to glaucophane and with a gentle slope to the calcic amphibole field; there is no indication of any termination of the solvus under the pressure-temperature conditions of crystallization of the Ouégoa schists.     

Mineralogy of New Caledonian metamorphic rocks

Variations in chemistry and related physical properties of sheet silicates in the Ouégoa district with metamorphic grade are investigated. Weakly metamorphosed rocks prior to the crystallization of lawsonite contain phengite (d ₀₀₆=3.317–3.323 Å), chlorite and occasionally paragonite while interstratified basaltic sills contain chlorite, minor phengite and stilpnomelane. Pyrophyllite crystallizes before lawsonite in some metamorphosed acid tuffs and is also stable in the lawsonite zone. Paragonite, phengite and chlorite appear to be stable through the sequence from weakly metamorphosed rocks into high-grade “eclogitic” schists and gneisses. Optical, chemical and some X-ray diffraction data is given for representative sheet silicates. Electron probe analyses of 55 phengites, 21 paragonites, 57 chlorites, 12 vermiculites, 2 stilpnomelanes, and 2 chloritoids are presented in graphical form. All K-micas analysed are consistently phengitic (3.29–3.55 Si^iv ions per formula unit) and show limited solid solution with paragonite (4 to 13% Pa). The K∶Na ratio of the phengite is strongly dependant on the assemblage in which it occurs; the amount of phengite component and its Fe∶Mg ratio depends on bulk-rock composition. Phengites from acid volcanics have the highest Fe∶Mg ratio, highest phengite component and β refractive indices. Phengites from basic volcanics and metasediments of the epidote zone have the lowest Fe∶Mg ratio. Phengites from lawsonite-zone metasediments have intermediate Fe∶Mg ratios. The phengites show a small decrease in phengite component with increasing metamorphic grade. d ₀₀₆ for phengites varied from 3.302 to 3.323 Å but at least in the lawsonite and epidote zones appears to reflect composition and had little systematic variation with metamorphic grade; phengites from very low-grade rocks showed the longest values of d ₀₀₆. Paragonite shows almost no phengite-type substitution and only limited solid solution (4–12%) with muscovite. All paragonites (6) and most phengites (20) which have been examined are 2M₁ polymorphs; one Fe²⁺-phengite appears to be a 1M polymorph. The chemistry of chlorites closely reflects parent-rock chemistry. Chlorites from metasediments have distinctly higher Fe/(Fe+Mg) ratios than chlorites from basic igneous rocks; chlorites from the lawsonite and lawsonite-epidote transitional zone metasediments have the highest Fe/(Fe+Mg) ratios. In metabasalts Fe/(Fe+Mg) ratios appear to reflect individual variations in bulk-rock chemistry and show no direct correlation with metamorphic grade. There is little difference in Al/(Si+Al) ratio between chlorites from sediments and basic igneous rocks although in both lithologies the chlorites from the epidote zone appear to be slightly more aluminous. Fe-rich chlorites of the lawsonite zone metasediments have been altered by a process involving leaching of Fe and Mg and introduction of alkalies to a brown pleochroic Fe-vermiculite. Chemical and physical data for this vermiculite are given. The decrease in Fe/(Fe+Mg) ratio in chlorites and phengites on passing from the lawsonite to the epidote zone can be correlated with the crystallization of Fe-rich epidote and almandine in the epidote zone. Elemental partitioning between coexisting minerals has shown Ti to be partitioned into phengite, while Fe and Mn are strongly partitioned into chlorite. When either stilpnomelane or chloritoid coexists with phengite or chlorite, Fe and Mn are slightly enriched in the stilpnomelane or chloritoid relative to the chlorite.     

Mineralogy of New Caledonian metamorphic rocks

The compositions of metamorphic pyroxenes from blueschists in northern New Caledonia are investigated. Aegerine-augite occurs in siliceous metasediments and aegerine in some low-grade sodic basic schists. Calcic metamorphic pyroxene (omphacite and chloromelanite) appears first in metabasalts in higher grades of the lawsonite zone and is widespread in metamorphosed igneous rocks and quartzofeldspathic gneisses of the epidote zone. Omphacites in basic rocks have higher Mg∶Fe ratios and are less jadeitic than omphacites from adjacent interbedded quartzofeldspathic gneisses. With increasing metamorphic grade pyroxenes become more jadeitic and diopsidic at the expense of their acmite component. Elemental partitioning between coexisting pyroxenes, garnets and amphiboles from in situ regional metamorphic rocks is generally regular, suggesting equilibrium crystallization. Omphacite appears to be a stable phase within blueschist facies over a temperature range of at least 350° to 550° C. The “eclogitic” assemblage almandine-omphacite is stable within the earth's crust in metamorphosed sediments and igneous rocks over a temperature range of 400° to at least 550° C. No estimate of absolute pressures involved in metamorphism in the Ouégoa district can yet be made.     

Oxygen isotope study of metamorphic rocks from the Ouégoa district,New Caledonia

48 minerals from 18 in situ metamorphic rocks (mostly metasediments) from the Ouégoa district have been studied. Particular emphasis was placed on obtaining isotopic data for quartz, calcite and muscovite but some pyroxenes and amphiboles were also examined. Data for Ouégoa rocks show they have tended to be isotopically homogenized by metamorphism and that the effect of increasing metamorphism is to progressively deplete the rocks of heavy C and O isotopes. These results indicate that during metamorphism the rocks isotopically exchanged through the medium of a widespread oxygen-carrying fluid phase. Tentatively assigned temperatures obtained from isotopic data for quartz-calcite and quartz-muscovite pairs, using the calibration curves of Epstein and Taylor (1967), indicate lawsonite in the Ouégoa schists to be stable over a temperature range of 250 to 400° C and epidote from ca. 380° to at least 550° C. Temperatures for metamorphic zones in Ouégoa blueschists closely parallel those obtained for Type III and IV glaucophane-bearing rocks from Ward Creek, California (Taylor and Coleman, 1968). The measured tectonic thickness of lawsonite-bearing schists has been used to calculate a lithostatic pressure increment of 2 Kb and geothermal gradient of 20° C per km for the lawsonite zone. Comparison of lithostatic pressure increment with total pressure increment estimated from the stability relations of lawsonite over the temperature range 250–400° C (3.5 Kb Nitsch, 1972) suggest P _total ≠ P _lithostatic and that that the pressure of the fluid phase may have exceeded lithostatic pressure.     

The genesis of garnet and cordierite in acid volcanic rocks: Evidence from the Cerberean Cauldron,Central Victoria,Australia

In the acid volcanic rocks of the Cerberean Cauldron of Central Victoria, four almandine garnet types can be distinguished. Types 1 and 2 are the most important. Type 1 garnets, about 1 mm across, euhedral and free of inclusions, occur mainly in the Rubicon Rhyolite. Type 2 garnets, up to 1 cm across, often irregular and always with inclusions, are most abundant in the Lake Mountain Rhyodacite. Type 1 garnets are enriched in Fe and Mn and depleted in Mg and Ca with respect to Type 2 garnets. Zoning patterns in Type 1 garnets show enrichment of Fe and Mn in the cores. Conversely Type 2 garnets have Fe and Mn enriched rims, although the zoning is frequently less regular. Fe rich cordierite occurs, mainly in the Rubicon Rhyolite, as nearly euhedral sixlings, without inclusions. They are frequently altered but where fresh show zoning patterns like those of the Type 1 garnets.These characteristics are best explained if the Type 2 garnets and cordierite are residuals of high grade metamorphic assemblages in granitic liquids produced by partial melting of pelitic rocks. Type 1 garnets and biotite subsequently crystallized from the liquid and the zoning patterns of Type 2 garnets and cordierite were modified near their rims by reaction.     

Garnet Types from the Cazadero Area, California

This is the third in a series of papers on glaucophane schistsfrom the Franciscan Formation near Cazadero, California. Previouspapers describe three distinct types of glaucophane-bearingFranciscan metamorphic rocks near Cazadero. The purpose of this study is to investigate the garnets presentin metamorphic types III (bedrock schists) and IV (tectonicblocks) as defined by Coleman & Lee (1963). Twenty-fourgarnet analyses are presented. Sixteen of these are from (aragonite-bearing)type III glaucophane schists, and eight are from type IV glaucophaneschists. Type IV rocks include California eclogites. Type III rocks include metabasalt, metachert, metashale, meta-ironstone,and metacarbonate that were formed under high pressure and relativelylow temperature. These rocks contain garnets that display awide range of composition, but the dominant molecules representedare consistently almandine, spessartine, and grossular. Type IV rocks are mainly metabasalts that were probably formedunder higher temperatures and pressures than type III rocks.There is a distinct difference between garnets from type IIIrocks and those from type IV (including eclogites); the lattercontainless spessartine and more pyrope, and the dominant moleculesare almandine and grossular. The four analyses of garnets fromCalifornia eclogites have an average pyrope content of aboutten molecular per cent, and they extend the range of compositionreported for eclogite garnets. Quantitative spectrographic determinations of minor elementsare listed for each of the garnets described. The values determinedfor some of the minor elements have a wide range and a capriciousdistribution over a few feet of outcrop area. As a group, both the garnets from type III rocks and those fromtype IV are pyralspites with large contents (as much as 35 molecularper cent) of ugrandite. This unusual admixture of the pyralspiteand ugrandite garnet series may have resulted in part from theconditions (high pressures and relatively low temperatures)under which the enclosing rocks were recrystallized.     

Regional progressive high-pressure metamorphism, Seward Peninsula, Alaska

Abstract Blueschist-facies rocks on the Seward Peninsula constitute a structurally coherent terrane measuring at least 100 × 150 km. Radiometric age data indicate that high-pressure metamorphism probably occurred in Jurassic rather than in Palaeozoic or Precambrian time, as previously suggested. Protolith sediments (Nome Group) are of intracontinental basin or continental margin type, and of lower Palaeozoic and possibly late Precambrian age, thus predating the high pressure metamorphism by more than 200 m.y. Blueschist-facies mineral assemblages were developed in almost all lithologies of the Nome Group, and are best preserved in FeTi-rich metabasites (glaucophane + almandine + epidote) and pelites (glaucophane + chloritoid + phengite). A lawsonite–crossite subfacies was developed in possible Nome Group rocks on the east flank of the Darby Mountains. Albite–epidote–amphibolite facies assemblages characterize Nome Group rocks in the southwestern part of the Peninsula. Metamorphism in the central zone of the terrane passed from early lawsonitic to subsequent epidote–almandine–glaucophane schist subfacies with the local development (east of the Nome River) of eclogitic assemblages. The high pressure metamorphic minerals were synkinematic with the development of mesoscopic-scale intrafolial isoclinal folds and a flattening foliation of consistent orientation. Initiation of uplift probably corresponded to the growth of barroisite rims on earlier sodic and actinolitic amphiboles, and partial post-kinematic greenschist facies replacements record later stages of decompression. Ophiolites and melange are not associated with the Seward Peninsula blueschists. The high-pressure metamorphism was caused by tectonic loading of a continental plate by an allochthon of indeterminate origin. The PT conditions of high pressure metamorphism were approximately 9–11 kbar, 400–450°C, thus falling between the PT paths of the Shuksan and Franciscan terranes.     

New data on the metamorphic petrology of rocks from the Kuekvun uplift (Northern Chukchi Peninsula)

The metamorphic rocks of the Kuekvun uplift are gneisses and schists that developed after Mid-Paleozoic sedimentary sequences, which consist mostly of terrigenous rocks with minor amounts of intermediate to mafic igneous rocks and subordinate carbonates. Two plagiogneiss samples that were selected for detailed analysis were taken from the axial part and flanks of the uplift. The mineral paragenesis and composition of coexisting garnet, biotite, and staurolite indicate a metamorphic temperature of 560–600°C and pressure of 2.5–4 kbar, corresponding to a depth of 8–12 km. These conditions suggest a relatively high geothermal gradient (about 60°C/km), approaching that for contact metamorphic aureoles. Garnets from the axial zone and flanks of the uplift display a similar zoning pattern. The difference is the presence of compositionally contrasting Ca-rich rims in garnets from the axial zone. These rims may be either the result of zoning within the entire metamorphic complex or a late local overprint, e.g., crystallization of granitic plutons, which are common within the study area.     

Lawsonite growth in the epidote blueschists from the Ile de Groix (Armorican Massif, France): a potential geobarometer

Abstract The garnet blueschists from the Ile de Groix (Armorican Massif, France) contain millimetre‐ to centimetre‐sized pseudomorphs consisting of an aggregate of chlorite, epidote and paragonite. The pseudomorphed phase developed at a late stage of the deformation history, because it overgrows a glaucophane–epidote–titanite foliation. Garnet growth occurred earlier than the beginning of the ductile deformation, and thus garnet is also included in the pseudomorphs. Microprobe analyses show that garnet is strongly zoned, with decreasing spessartine and increasing almandine and pyrope contents from core to rim. Grossular content is higher in garnet cores (about 35 mole%) compared to garnet rims (about 30 mole%). Blue amphibole has glaucophane compositions with a low Fe³⁺ content and become more magnesian when inclusions in garnet (X_Mg = 0.62–0.65) are compared with matrix grains (X_Mg = 0.67–0.70). Matrix epidote has a pistacite content of about 50 mole%. On the basis of their shape and the nature of the breakdown products, the pseudomorphs are attributed to lawsonite. A numerical model (using Thermocalc ) has been developed in order to understand the reactions controlling both the growth and the breakdown of lawsonite. Lawsonite growth could have taken place through the continuous hydration reaction Chl + Ep + Pg + Qtz + Vap = Gln + Lws, followed by the fluid‐absent reaction Chl + Ep + Pg = Grt + Gln + Lws. Peak P–T conditions are estimated at about 18–20 kbar, 450 °C. This indicates that lawsonite growth took place at increasing P and T, hence can be used as a geobarometer in the buffering assemblage garnet–glaucophane–epidote. The final part of the history is recorded by lawsonite breakdown, after cessation of the ductile deformation, and recording the earliest stages of the exhumation.     

Garnet compositions and their use as indicators of peraluminous granitoid petrogenesis — southeastern Arabian Shield

Garnet, an uncommon accessory mineral in igneous rocks, occurs in seven small peraluminous granitoid plutons in the southeastern Arabian Shield; textural equilibrium between garnet and other host granitoid minerals indicates that the garnets crystallized from their host magmas. Compositions of the garnets form three groups that reflect host-granitoid compositions, which in turn reflect source compositions and tectonic regimes in which the host magmas were generated. Garnets from the seven plutons have almandine-rich cores and spessartine-rich rims. This reverse zoning depicts host magma compositional evolution; i.e. rimward spessartine enrichment resulted from progressive, host-magma manganese enrichment. The garnets are heavy rare-earth element enriched; (Lu/La) _N ranges from 13 to 355 and one of the garnets contains spectacularly elevated abundances of Y, Ta, Th, U, Zn, Zr, Hf, Sn, and Nb. Involvement of garnets with these trace element characteristics in magma genesis or evolution can have dramatic effects on trace element signatures of the resulting magmas. Other researchers suggest that Mn-enriched magmas are most conducive to garnet nucleation. Although the garnetiferous granitoids discussed here are slightly Mn enriched, other genetically similar peraluminous Arabian granitoids lack garnet; Mn enrichment alone does not guarantee garnet nucleation. The presence of excess alumina in the magma may be a prerequisite for garnet nucleation.     

Compositional characteristics of garnets and pyroxenes in contact-metasomatic skarn deposits and their relationship with metallization

The compositions of more than 300 granets and pyroxenes from 14 contact-metasomatic calcic skarn deposits and calcic-magnesia skarn skarn deposits in China have been examined using electron microprobe technique. The compositions of garnets and pyroxenes from a wide variety of ore types represent ten major classes of calcic skarn deposits (Fe, Fe-Cu, Pb-Zn,W, Sn, Sn-Mo-Bi-W, W-Bi-Cu-Mo, Cu-Zn and W-Zn-Cu) and three major classes of calcic-magnesia skarn deposits (Fe-Cu, Mo, Pb-Zn). Garnets and pyroxenes show a wide range of variation in composition, but the majority of garnets are grossular-andradite solid solutions containing less than 15 mol% (spessartine + almandine + pyrope), whereas most pyroxenes are diopside-hedenbergite solid solutions containing less than 5 mol% johannesenile. Some pyroxenes from a Pb-Zn calcic-magnesia skarn deposit display an increase in Mn content. Only Sn-W calcic skarn deposits and Pb-Zn calcic-magnesia skarn deposits contain garnets with more than 15 mol% (spessartine + almandine + pyrope). Some relationships have been established between the compositions of garnets and pyroxenes and the metallization types of economically important metals in skarn deposits.     

The genetic significance of almandine-pyrope phenocrysts in the calc-alkaline Borrowdale Volcanic Group,Northern England

A suite of garnet-bearing andesites and dacites from the Ordovician of N. W. England is described and major- and trace-element analyses of the garnet phenocrysts are presented. The garnets are of almandine-pyrope composition, with minor amounts of spessartine and grossular, and often show marked reversed zoning; the crystal becoming progressively enriched in pyrope towards the margin. Garnets from the dacites are consistently richer in almandine and spessartine than are those from the andesites.From a consideration of the chemistry of the garnet phenocrysts and host rocks, especially La and Y abundances, it is shown that garnet could not have been removed from the magma in quantities sufficient to affect the liquid composition. Consequently the magma must have evolved by some process other than crystal fractionation. It is proposed that the magma was generated by the partial melting of oceanic crust along an ancient Benioff zone, stored at depth (possibly at the crust/mantle interface) long enough for garnet to nucleate, and then transferred rapidly to the surface. Isobaric crystallisation of the garnet phenocrysts at depth could explain the reversed zoning observed.     

Die Glaukophangesteine,ihre stofflichen Äquivalente und Uniwandlungsprodukte in Nordcalabrien (Süditalien)

In the southern Apennin (= northern part of the region dealt with) and the Coasta Chain (= southern part) there are metabasalts wich are classified in the northern part as:

1. Glaucophane rocks of the albite-lawsonite-glaucophane-subfacies with the assemblage glaucophane + pumpellyite + lawsonite ±albite ±aragonite ±muscovite (7 rock analyses, 8 mineral analyses). These rocks are conceived as relics of an older burial metamorphism.
2. Rocks with pumpellyite and chlorite or also chlorite alone, that are interpreted as reaction rims between the metastable glaucophane rocks and the country rock (phyllites, quartzites). The assemblages pumpellyite + chlorite and chlorite alone are to be found (2 rock analyses and 2 mineral analyses).
3. Rocks with lawsonite and/or epidote belong to the same mineral facies as the country rock: a facies similar to the greenschist facies (called “lawsonite-albite-chlorite-subfacies”) which is characterized by the assemblages lawsonite + albite + chlorite ±calcite and also epidote ±lawsonite + albite + chlorite ± muscovite. These types are attributed to a younger dynamo-metamorphism (2 rock analyses).

In the southern part, the metabasalts can be found only as rocks with epidote and/or lawsonite, a metamorphism with more than one event cannot be proved petrologically (3 rock analyses). Equations of the observed mineral reactions are given. The transitions of one facies into another are represented in the pseudo-quaternary system Al₂O₃-CaO-Na₂O · Al₂O₃-2 Fe₂O₃ + FeO + MnO + MgO-(H₂O). The pressure-temperature conditions are estimated on the basis of published experimental data (300° C and 6–7 kb for the glaucophane rocks; 400° C and about 6 kb for the rocks with lawsonite and/or epidote) and are compared with geologic facts.     

Mineralogy,petrology, and phase relations of glaucophane-lawsonite zone blueschists from the Tavşanli Region,Northwest Turkey

Glaucophane-lawsonite facies blueschists representing a metamorphosed sequence of basic igneous rocks, cherts and shales have been investigated northeast of the district of Tav?anli in Northwest Turkey. Sodic amphiboles are rich in magnesium reflecting the generally high oxidation states of the blueschists. Lawsonite has a very uniform composition with up to 2.5 wt.% Fe₂O₃. Sodic pyroxenes show an extensive range of compositions with all the end-members represented. Chlorites are uniform in their Al/(Al+Fe+Mg) ratio but show variable Fe/ (Fe+Mg) ratios. Garnets from metacherts are rich in spessartine (>50%) whereas those from metabasites are largely almandine. Pistacite rich epidote is found in metacherts coexisting with lawsonite. Phengites are distinctly higher in their Fe, Mg and Si contents than those from greenschist facies. Hematites with low TiO₂ are ubiquitous in metacherts. Fe²⁺/Mg partitioning between chlorite and sodic amphibole is strongly controlled by the calcium content of the sodic amphibole and ranges from 1.1 for low calcium substitution to 0.8 for higher calcium substitution. The Al/Fe³⁺ partition coefficient between sodic amphibole and sodic pyroxene is 2.1. A model system has been constructed involving projections from lawsonite, iron-oxide and quartz onto a tetrahedron with Na, Al, Fe²⁺ and Mg at its apices. Calcite is treated as an indifferent phase. The model system illustrates the incompatibility of the sodic pyroxene with chlorite in the glaucophanelawsonite facies; this assemblage is represented by sodic amphibole. Sodic amphibole compositions are plotted in terms of coexisting ferromagnesian minerals. Five major areas on the sodic amphibole compositional field are delineated, each associated with one of the following minerals: chlorite, stilpnomelane, talc, almandine, deerite.     

接触交代夕卡岩型矿床中石榴子石和辉石成分特点及其与矿化的关系

本文对中国十四个接触交代钙夕卡岩矿床和钙-镁夕卡岩矿床中的三百多个样品的石榴子石和辉石成分进行了电子探针分析。不同矿床类型的石榴子石和辉石成分代表着钙夕卡岩矿床的十个矿种(Fe、Fe-Cu、Pb-Zn、W、Sn、Sn-Mo-Bi-W、、W-Bi-Cu-Mo、Cu-Zn、Cu-Sn、W-Zn-Cu)和钙-镁夕卡岩矿床的三个矿种(Fe-Cu、Mo、Pb-Zn)。石榴子石和辉石成分变化范围大,大多数石榴子石是含锰铝榴石+铁铝榴石+镁铝榴石小于15％(摩尔百分数)的钙铝榴石-钙铁榴石固溶体;大多数辉石是含小于5％的锰钙辉石的透辉石-钙铁辉石固溶体。有些Pb-Zn钙-镁夕卡岩矿床中的辉石显示出Mn含量有所增加。只有Sn和W钙夕卡岩矿床及Pb-Zn钙-镁夕卡岩矿床含(Sps+Alm+Pyr)总量大于15％的石榴子石。石榴子石和辉石成分与夕卡岩矿床金属矿化类型之间有某些联系。     

<Emphasis Type="Italic">P-T</Emphasis> conditions of the Jandagh metapelitic schists,Northeastern Isfahan Province,Iran

The metapelitic schists of Jandagh or simply Jandagh metapelites can be divided into four groups based on mineral assemblages: (1) quartz-muscovite schists, (2) quartz-muscovite-biotite schists, (3) garnet-muscovite-chlorite schists, and (4) garnet-muscovite-staurolite schists. The Jandagh garnet-muscovite-chlorite schists show the first appearance of garnets. These garnets contain 58–76% almandine, 1–18% spessartine, and 8–20% grossular. Microprobe analysing across the garnets demonstrates an increase in Mg# from core to rim. This is a feature of the prograde metamorphism of metapelites. Well-preserved garnet growth zoning is a sign that metapelites were rapidly cooled and later metamorphic phases had no effect here. The appearance of staurolite in garnet-muscovite-chlorite schists signifies a beginning of the amphibolite facies. The absence of zoning in staurolite suggests that its formation and growth during prograde metamorphism occurred at a widely spaced isograde. Thermobarometric investigations show that the Jandagh metapelites were formed within a temperature range of 400–670°C and pressures of 2.0–6.5 kbar. These results are in agreement with the mineral paragenetic evidence and show the development of greenschist and amphibolite facies in the area studied.     

Cold subduction of the Neotethys: the metamorphic record from finely banded lawsonite and epidote blueschists and associated metabasalts of the Nagaland Ophiolite Complex,India

In this study, we have deduced the thermal history of the subducting Neotethys from its eastern margin, using a suite of partially hydrated metabasalts from a segment of the Nagaland Ophiolite Complex (NOC), India. Located along the eastern extension of the Indus‐Tsangpo suture zone (ITSZ), the N–S‐trending NOC lies between the Indian and Burmese plates. The metabasalts, encased within a serpentinitic mélange, preserve a tectonically disturbed metamorphic sequence, which from west to east is greenschist (GS), pumpellyite–diopside (PD) and blueschist (BS) facies. Metabasalts in all the three metamorphic facies record prograde metamorphic overprints directly on primary igneous textures and igneous augite. In the BS facies unit, the metabasalts interbedded with marble show centimetre‐ to metre‐scale interlayering of lawsonite blueschist (LBS) and epidote blueschist (EBS). Prograde HP/LT metamorphism stabilized lawsonite + omphacite (X_Jd = 0.50–0.56 to 0.26–0.37) + jadeite (X_Jd = 0.67–0.79) + augite + ferroglaucophane + high‐Si phengite (Si = 3.6–3.65 atoms per formula unit, a.p.f.u.) + chlorite + titanite + quartz in LBS and lawsonite + glaucophane/ferroglaucophane ± epidote ± omphacite (X_Jd = 0.34) + chlorite + phengite (Si = 3.5 a.p.f.u.) + titanite + quartz in EBS at the metamorphic peak. Retrograde alteration, which was pervasive in the EBS, produced a sequence of mineral assemblages from omphacite and lawsonite‐absent, epidote + glaucophane/ferroglaucophane + chlorite + phengite + titanite + quartz through albite + chlorite + glaucophane to lawsonite + albite + high‐Si phengite (Si = 3.6–3.7 a.p.f.u.) + glaucophane + epidote + quartz. In the PD facies metabasalts, the peak mineral assemblage, pumpellyite + chlorite + titanite + phengitic white mica (Si = 3.4–3.5 a.p.f.u.) + diopside appeared in the basaltic groundmass from reacting titaniferous augite and low‐Si phengite, with prehnite additionally producing pumpellyite in early vein domains. In the GS facies metabasalts, incomplete hydration of augite produced albite + epidote + actinolite + chlorite + titanite + phengite + augite mineral assemblage. Based on calculated T–M(H₂O), T–M(O₂) (where M represents oxide mol.%) and P–T pseudosections, peak P–T conditions of LBS are estimated at ~11.5 kbar and ~340 °C, EBS at ~10 kbar, 325 °C and PD facies at ~6 kbar, 335 °C. Reconstructed metamorphic reaction pathways integrated with the results of P–T pseudosection modelling define a near‐complete, hairpin, clockwise P–T loop for the BS and a prograde P–T path with a steep dP/dT for the PD facies rocks. Apparent low thermal gradient of 8 °C km^?1 corresponding to a maximum burial depth of 40 km and the hairpin P–T trajectory together suggest a cold and mature stage of an intra‐oceanic subduction zone setting for the Nagaland blueschists. The metamorphic constraints established above when combined with petrological findings from the ophiolitic massifs along the whole ITSZ suggest that intra‐oceanic subduction systems within the Neotethys between India and the Lhasa terrane/the Karakoram microcontinent were also active towards east between Indian and Burmese plates.     

Petrology of some Glaucophane Schists and Related Rocks from Taiwan

Detailed laboratory study has been made on pre-Tertiary coarse-grainedglaucophane schist, garnet-epidote amphibolite, and epidoteamphibolite in the eastern slope of the Central Mountain Range,Taiwan. These petrotectonic assemblages are considered to beexotic tectonic blocks emplaced within the feebly metamorphosedin situ graphite and quartzose schists of the Yuli belt. Thinlenses of Mn-rich metamorphosed tuff are intercalated withinthe metabasaltic rocks. Such high MnO (2 wt. per cent) and lowMgO (3–4 wt. per cent) tuffaceous rocks are similar inbulk composition to some volcanic clays collected in deep oceanbasins. They consist of the characteristic assemblage Mn-bearinggarnet (5–7 wt. per cent MnO and 30 volume per cent inthe rock)+muscovite+epidote+hornblende+quartz+ albite+rutile?pyrite. Successive stages of conversion of garnet-epidote amphiboliteto blueschist assemblages were noticed. The most recrystallizedschists display abundant Mn-bearing garnet, zoned amphibole,phengite, zoned epidote, stilpnomelane, chlorite, quartz, minoralbite, magnetite, and sphene. The recrystallization processis nearly isochemical except the glaucophane schists appearto be more oxidized and contain more Na₂O than the relict amphibolites.Intimately associated amphibolites of basaltic composition,in contrast, contain the assemblage hornblende+paragonite+epidote+chlorite+quartz+albite+rutile. Microprobe analyses of the coexisting minerals in glaucophaneschists, garnet-epidote amphibolites and epidote amphibolitesyield the following results: (1) garnets, consisting of almandine,spessartine, and grossular components, are less Mn and Mg-richcompared to those in in situ metabasalts of the Franciscan;(2) rim epidotes of the glaucophane schists are more pistastic(X_Fe=0?27–0?30) than that of the garnet-epidote amphibolite(0?2–0?22) implying higher fO₂ values for the glaucophanization;(3) phengitic micas of the glaucophane schist have less Al₂O₃content (29 wt. per cent) than those of the garnet-epidote amphibolite(32 wt. per cent) whereas micas of epidote amphibolites areparagonites with K/(K+Na) ratio of 0?04; (4) the zoned amphibolesshow glaucophane occurring marginal to cores of calcic amphibole.Sodic amphiboles with Al₂O₃ of 6-? to 10?4 wt. per cent arecrossite-glaucophane whereas all calcic amphiboles analyzedare barroisite-pargasite (Al₂O₃ greater than 10 wt. per cent). The garnet-epidote-rutile bearing glaucophane schist of Taiwanprobably recrystallized at temperatures above 350 ?C (the epidotezone) whereas the lawsonite-sphene glaucophane schists of theFranciscan equilibrated below 350 ?C (the lawsonite zone). TheMn-rich basaltic tuffs and their associated flows appear tohave been metamorphosed at profound depths and at the relativelyhigh temperatures of the epidote amphibolite facies, succeededlater by glaucophane schist facies metamorphism at lower temperatures.     

高压-超高压变质岩石中不同成因的石榴石

石榴石是高压-超高压变质岩石中最重要的变质矿物之一,是研究俯冲带深部变质和熔融过程的理想研究对象.通过对俯冲带内不同条件下形成的石榴石进行详细研究,确定了岩浆成因、变质成因和转熔成因石榴石.岩浆石榴石是岩浆熔体在冷却过程中结晶形成,成分主要为锰铝榴石-铁铝榴石,通常含有石英、长石、磷灰石等晶体包裹体.变质石榴石是在亚固相条件下通过变质反应形成,包裹体为参与变质反应的矿物组合;进变质生长的石榴石通常显示核部到边部锰铝榴石降低的特征.转熔石榴石是在超固相条件下通过转熔反应形成,通常含有晶体包裹体,其中既有从转熔熔体结晶的矿物包裹体,也有转熔反应残留的矿物包裹体.对超高压变质岩石中转熔石榴石的识别,可以为深俯冲陆壳岩石的部分熔融提供重要的岩石学证据,是大陆俯冲带部分熔融研究的重要进展之一.      

Retrograde zoning in garnets of Elat-Wadi Magrish metamorphic rocks

Garnets of the progressively metamorphosed Elat-Wadi Watir metasediments show an inverse zonation; MnO concentration is relatively higher at the margins than in the center of the crystals while MgO shows the opposite trend. The zoning is probably caused by a retrograde metamorphism during which the garnet was partly replaced by chlorite. The control of the temperature from which garnets began to cool on zoning effectiveness is discussed.