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1.
The Connemara ophicalcites and associated marbles contain varyingproportions of calcite, dolomite, tremolitic amphibole, serpentinizedolivine, diopside, humite, phlogopite, clinochlore, and quartz.They formed from a chemically precipitated 'primary' dolomitewith a small amount of mica and clay minerals in which muchof the trace and minor element content of the rock, e.g. Al,Fe, Ti, Zn, Ni, Cr, Zr, K, Rb, and rare earths was concentrated.The rock was probably silicified after deposition, possiblyduring metamorphism, and was probably not deposited with majoradmixed detrital quartz or feldspar. The formation during metamorphismof complementary segregated layers rich in either olivine (Fo98±2)or calcite resulted from important chemical changes controlledby the composition of the stable metamorphic minerals, i.e.those for which solution concentrations exceeded the solubilityproduct for the pore fluid. The mineralogy influenced the localconcentrations of both major and trace elements and emphasizesthe importance of solutions and the stable metamorphic mineralogyin manipulating the composition of some metamorphic rocks. Somecriteria for recognizing segregated layers in metamorphic rocksare given. Serpentinization was probably by addition of water and silicaand not by movement of Fe or Mg. Chemical analyses of forty-threesamples each for twenty-six oxides and elements are given andthe first occurrence of humite in Connemara is reported.  相似文献   

2.
Marble occurs abundantly in a 31,000 km2 segment of the southernGrenville Province of the Canadian Precambrian Shield, whereit is associated with quartzite, biotite-garnet gneiss, andamphibolite to form the Grenville Group. An 1800 km2 area onthe western margin of this segment, north of the Ottawa river,displays a great variety of carbonate rocks, which may be dividedinto two groups: (I) major marble, with calcite, dolomite, graphite, phlogopite,Ca amphibole, Ca pyroxene, forsterite, humite group minerals, (II) minor marble, with pink calcite, phlogopite, Ca amphibole,Ca pyroxene, K feldspar, scapolite, sphene. Rocks of the first group are associated with plagioclase gneissand amphibolite, and are metamorphosed limestone, little affectedby metasomatism; rocks of the second group, which are less common,are associated with potassium feldspar gneiss and heterogeneousgranitic and syenitic rocks, and are inferred to be metasomaticrocks. Numerous mineral reactions have taken place in the carbonaterocks during metamorphism. The calcite-dolomite reaction, whichgoverns the Mg content of calcite, indicates a metamorphic temperatureof about 650 °C. Forsterite was possibly produced from low-Alamphibole, and forsterite + spinel from high-Al amphibole. Thecrystallization of some silicate minerals in the minor marbleunits, and the enrichment in the contained calcite in Fe andSr are attributed to metasomatic reactions. Metamorphic ion-exchangereactions involving carbonates produced the following distributioncoefficients: Sr in calcite/Sr in dolomite = 2.5 Mn in calcite/Mn in dolomite = 0.89 Fe in calcite/Fe in dolomite = 0.29 from which inferences may be drawn concerning the distributionof these elements between the Ca and Mg sites within dolomiteduring metamorphic crystallization. Ion-exchange reactions involvingsilicates produced the following distribution of Mn: humite group Ca pyroxene.Ca amphibole phlogopite where the numbers are distribution coefficients. An equilibriumdistribution of Fe between silicates and calcite in the minormarble was evidently not attained during metasomatic crystallization.Numerous retrograde reactions have taken place, including thealteration of pyroxene to amphibole, forsterite to serpentine,and the exsolution of dolomite from calcite. Forsterite in marble, and orthopyroxene in the associated gneissesand amphibolites crystallized sporadically in the Laurentianhighlands, but not in the lowlands of the Ottawa rift valley,where peak metamorphic temperatures may have been slightly lower.In the highlands, reactions to produce forsterite and orthopyroxenewere initiated in response to a local increase in temperature,local peculiarities in the chemical composition of amphibole,which produced these minerals, or a local decrease in the activityof CO2 and H2O in the grain-boundary phase.  相似文献   

3.
Scapolite and other halogen-rich minerals (phlogopite, amphibole,apatite, titanite and clinohumite) occur in some high-pressureamphibolite facies calc-silicates and orthopyroxene-bearingrocks at Sare Sang (Sar e Sang or Sar-e-Sang), NE Afghanistan.The calc-silicates are subdivided into two groups: garnet-bearingand garnet-free, phlogopite-bearing. Besides garnet and/or phlogopite,the amphibolite facies mineral assemblages in the calc-silicatesinclude clinopyroxene, calcite, quartz and one or more of theminerals scapolite, plagioclase, K-feldspar, titanite, apatiteand rarely olivine. Orthopyroxene-bearing rocks consist of clinopyroxene,garnet, plagioclase, scapolite, amphibole, quartz, calcite andaccessory dolomite and alumosilicate (kyanite?). Retrogradephases in the rocks are plagioclase, scapolite, calcite, amphibole,sodalite, haüyne, lazurite, biotite, apatite and dolomite.The clinopyroxene is mostly diopside and rarely also hedenbergite.Aegirine and omphacite with a maximum jadeite content of 29mol % were also found. Garnet from the calc-silicates is Grs45–95Py0–2and from the orthopyroxene-bearing rocks is Grs10–15Py36–43.Peak P–T metamorphic conditions, calculated using availableexchange thermobarometers and the TWQ program, are 750°Cand 1·3–1·4 GPa. Depending on the rock type,the scapolite exhibits a wide range of composition (from EqAn= 0·07, XCl =0·99 to EqAn = 0·61, XCl =0·07).Equilibria calculated for scapolite and coexisting phases atpeak metamorphic conditions yield XCO2 = 0·03–0·15.XNaCl (fluid), obtained for scapolite, ranges between 0·04and 0·99. Partitioning of F and Cl between coexistingphases was calculated for apatite–biotite and amphibole–biotite.Fluorapatite is present in calc-silicates, but orthopyroxene-bearingrocks contain chlorapatite. Cl preferentially partitions intoamphibole with respect to biotite. All these rocks have sufferedvarious degrees of retrogression, which resulted in removalof halogens, CO2 and S. Halogen- and S-bearing minerals formedduring retrogression and metasomatism are fluorapatite, sodalite,amphibole, scapolite, clinohumite, haüyne, pyrite, andlazurite, which either form veins or replace earlier formedphases. KEY WORDS: scapolite; fluid composition; high-pressure; amphibolite facies; Western Hindukush; Afghanistan  相似文献   

4.
FREY  MARTIN 《Journal of Petrology》1978,19(1):95-135
The unmetamorphosed equivalents of the regionally metamorphosedclays and marls that make up the Alpine Liassic black shaleformation consist of illite, irregular mixed-layer illite/montmorillonite,chlorite, kaolinite, quartz, calcite, and dolomite, with accessoryfeldspars and organic material. At higher grade, in the anchizonalslates, pyrophyllite is present and is thought to have formedat the expense of kaolinite; paragonite and a mixed-layer paragonite/muscovitepresumably formed from the mixed-layer illite/montmorillonite.Anchimetamorphic illite is poorer in Fe and Mg than at the diageneticstage, having lost these elements during the formation of chlorite.Detrital feldspar has disappeared. In epimetamorphic phyllites, chloritoid and margarite appearby the reactions pyrophyllite + chlorite = chloritoid + quartz+ H2O and pyrophyllite + calcite ± paragonite = margarite+ quartz + H2O + CO2, respectively. At the epi-mesozone transition,paragonite and chloritoid seem to become incompatible in thepresence of carbonates and yield the following breakdown products:plagioclase, margarite, clinozoisite (and minor zoisite), andbiotite. The maximum distribution of margarite is at the epizone-mesozoneboundary; at higher metamorphic grade margarite is consumedby a continuous reaction producing plagioclase. Most of the observed assemblages in the anchi-and epizone canbe treated in the two subsystems MgO (or FeO)-Na2O–CaO–Al2O3–(KAl3O5–SiO2–H2O–CO2).Chemographic analyses show that the variance of assemblagesdecreases with increasing metamorphic grade. Physical conditions are estimated from calibrated mineral reactionsand other petrographic data. The composition of the fluid phasewas low in XCO2 throughout the metamorphic profile, whereasXCH4 was very high, particularly in the anchizone where aH2Owas probably as low as 0.2. P-T conditions along the metamorphicprofile are 1–2 kb/200–300 °C in the anchizone(Glarus Alps), and 5 kb/500–550 °C at the epi-mesozonetransition (Lukmanier area). Calculated geothermal gradientsdecrease from 50 °C/km in the anchimetamorphic Glarus Alpsto 30 °C/km at the epi-mesozone transition of the Lukmanierarea.  相似文献   

5.
Upper Cretaceous phosphorite beds of the Duwi Formation, Upper Egypt, are intercalated with limestone, sandy limestone, marl, calcareous shales, and calcareous sandstone. Calcareous intercalations were subjected to field and detailed petrographic, mineralogical and geochemical investigations in order to constrain their rock composition and origin. Mineralogically, dolomite, calcite, quartz, francolite and feldspars are the non-clay minerals. Smectite, kaolinite and illite represent the clay minerals. Major and trace elements can be classified as the detrital and carbonate fractions based on their sources. The detrital fraction includes the elements that are derived from detrital sources, mainly clay minerals and quartz, such as Si, Al, Fe, Ti, K, Ba, V, Ni, Co, Cr, Zn, Cu, Zr, and Mo. The carbonate fraction includes the elements that are derived from carbonates, maily calcite and dolomite, such as Ca, Mg and Sr. Dolomite occurs as being dense, uniform, mosaic, very fine-to-fine, non-ferroan, and non-stoichiometrical, suggesting its early diagenetic formation in a near-shore oxidizing shallow marine environment. The close association and positive correlation between dolomite and smectite indicates the role of clay minerals in the formation of dolomite as a source of Mg^2＋ -rich solutions. Calcareous rocks were deposited in marine, oxidizing and weakly alkaline conditions, marking a semi-arid climatic period. The calcareous/argillaceous alternations are due to oscillations in clay/carbonate ratio.  相似文献   

6.
An extensive humite‐bearing marble horizon within a supracrustal sequence at Ambasamudram, southern India, was studied using petrological and stable isotopic techniques to define its metamorphic history and fluid characteristics. At peak metamorphic temperatures of 775±73°C, based on calcite‐graphite carbon isotope thermometry, the mineral assemblages suggest layer‐by‐layer control of fluid compositions. Clinohumite + calcite‐bearing assemblages suggest XCO2 < 0.4 (at 700°C and 5 kbar), calcite + forsterite + K‐feldspar‐bearing assemblages suggest XCO2>0.9 (at 790°C); and local wollastonite + scapolite + grossular‐bearing zones formed at XCO2 of c. 0.3. Retrograde reaction textures such as scapolite + quartz symplectites after feldspar and calcite and replacement of dolomite + diopside or tremolite+dolomite after calcite+forsterite or calcite+clinohumite are indicative of retrogression under high XCO2 conditions. Calcite preserves late Proterozoic carbon and oxygen isotopic signatures and the marble lacks evidence for extensive retrograde fluid infiltration, while during prograde metamorphism the possible infiltration of aqueous fluids did not produce significant isotopic resetting. Isotopic zonation of calcite and graphite grains was likely produced by localized CO2 fluid infiltration during retrogression. Contrary to the widespread occurrence of humite‐marbles related to retrograde aqueous fluid infiltration, the Ambasamudram humite‐marbles record a prograde‐to‐peak metamorphic humite formation and retrogression under conditions of low XH2O.  相似文献   

7.
The terrane in the Panamint Mountains, California, was regionallymetamorphosed under low-pressure conditions and subsequentlyunderwent retrograde metamorphism. Prograde metamorphic isogradsthat mark the stability of tremolite + calcite, diopside, andsillimanite indicate a westward increase in grade. The studywas undertaken to determine the effects of the addition of Caon the types of assemblages that may occur in pelitic schists,to contribute to the understanding of the stability limits inP – T – aH2O – XFe of the pelitic assemblagechlorite + muscovite + quartz, and to estimate the change inenvironment from prograde to retrograde metamorphism. Peliticassemblages are characterized by andalusite + biotite + stauroliteand andalusite + biotite + cordierite. Within a small changein grade, chlorite breaks down over nearly the entire rangein Mg/(Mg + Fe) to biotite + aluminous mineral. Chlorite withMg/(Mg + Fe) = 0.55 is stable to the highest grade, and thegeneralized terminal reaction is chlorite + muscovite + quartz= andalusite + biotite + cordierite + H2O. Calcic schists arecharacterized by the assemblage epidote + muscovite + quartz+ chlorite + actinolite + biotite + calcite + plagioclase atlow grades and by epidote + muscovite + quartz + garnet + hornblende+ biotite + calcite + plagioclase at high grades. Epidote doesnot coexist with any AFM phase that is more aluminous than garnetor chlorite. Lithostatic pressure ranged from 2.3 kb to 3.0kb. During prograde-metamorphism temperatures ranged from lessthan 400° to nearly 700°C, and XH2O (assuming PH2O +PCO3 = Ptotal) is estimated to be 0.25 in siliceous dolomite,0.8 in pelitic schist, and 1.0 in calcic schist. Temperatureduring retrograde metamorphism was 450° ± 50°C,and all fluid were H2O-rich. A flux of H2O-rich fluid duringfolding is believed to have caused retrograde metamorphism.The petrogenetic grid of Albee (1965b) is modified to positionthe (A, Cd) invariant point relative to the aluminosilicatetriple point, which allows the comparison of facies series thatinvolve different chloritoid-reactions.  相似文献   

8.
This study investigates marbles and calcsilicates in Central Dronning Maud Land (CDML), East Antarctica. The paleogeographic positioning of CDML as part of Gondwana is still unclear; however, rock types, mineral assemblages, textures and P–T conditions observed in this study are remarkably similar to the Kerala Khondalite Belt in India. The CDML marbles and calcsilicates experienced a Pan-African granulite facies metamorphism at c. 570 Ma and an amphibolite facies retrogression at c. 520 Ma. The highest grade assemblage in marbles is forsterite+spinel+calcite+dolomite, in calcsilicates the assemblages are diopside+spinel, diopside+garnet, scapolite+wollastonite+clinopyroxene±quartz, scapolite±anorthite±calcite+clinopyroxene+wollastonite. These assemblages constrain the peak metamorphic conditions to 830±20 °C, 6.8±0.5 kbar and X CO2>0.46. During retrogression, highly fluoric humite-group minerals (humite, clinohumite, chondrodite) replaced forsterite, and garnet rims formed at the expense of scapolite during reactions with wollastonite, calcite or clinopyroxene but without involvement of anorthite. Metamorphic conditions were about 650 °C, 4.5±0.7 kbar, 0.2< X CO2fluid<0.36, and the co-existence of garnet, clinopyroxene, wollastonite and quartz constrains fO2 to FMQ-1.5 log units. Mineral textures indicate a very limited influx of H2O-rich fluid during amphibolite facies retrogression and point to significant variations of fluid composition in mm-sized areas of the rock. Gypsum was observed in two samples; it probably replaced metamorphic anhydrite which appears to have formed under amphibolite facies conditions. The observed extensive anorogenic magmatism (anorthosites, A-type granitoids) and the character of metamorphism between 610 and 510 Ma suggest that the crustal thermal structure was characterized by a long-lived (50–100 Ma) rise of the crustal geotherm probably caused by magmatic underplating.  相似文献   

9.
The biotite isograd in pelitic schists of the Waterville Formationinvolved reaction of muscovite + ankerite + rutile + pyrite+graphite + siderite or calcite to form biotite + plagioclase+ ilmenite. There was no single reaction in all pelites; eachrock experienced a unique reaction depending on the mineralogyand proportions of minerals in the chlorite-zone equivalentfrom which it evolved. Quartz, chlorite, and pyrrhotite werereactants in some rocks and products in others. All inferredbiotite-forming reactions involved decarbonation and desulfidation;some were dehydration reactions and others were hydration reactions.P-T conditions at the biotite isograd were near 3500 bars and400 °C. C-O-H-S fluids in equilibrium with the pelitic rockswere close to binary CO2-H2O mixtures with XCO2 = 0.02–0.04.During the biotite-forming reaction, pelitic rocks (a) decreasedby 2–5 percent in volume, (b) performed – (4–11)kcal/liter P-V work on their surroundings, (c) absorbed 38–85kcal/liter heat from their surroundings, and (d) were infiltratedby at least 0.9–2.2 rock volumes H2O fluid. The biotite isograd sharply marks the limit of a decarbonationfront that passed through the terrane during regional metamorphism.Decarbonation converted meta-shales with 6–10 per centcarbonate to carbonate-free pelitic schists. One essential causeof the decarbonation event was pervasive infiltration of theterrane by at least 1–2 rock volumes H2O fluid early inthe metamorphic event under P-T conditions of the biotite isograd.Average shale contains 4–13 per cent siderite, ankerite,and/or calcite, but average pelitic schist is devoid of carbonateminerals. If the Waterville Formation serves as a general modelfor the metamorphism of pelitic rocks, it is likely that worldwidemany pelitic schists developed by decarbonation of shale caused,in part, by pervasive infiltration of metamorphic terranes byseveral rock volumes of aqueous fluid during an early stageof the metamorphic event.  相似文献   

10.
The mineralogy and geochemistry data are presented for thirty-seven shales,four concretions,two carbonate sediments and seven lignites from the Marathousa coal field of the Megalopolis Basin in Greece.The argillaceous rocks consist of chlorite,illite,kaolinte,albite,quartz.opal-A,calcite and dolomite;the concretions of aragonite,gypsum and pyrite;and the carbonate rocks of calcite,quartz and illite.The mineral matter in the lignites consists of gypsum,quartz,albite,chlorite,illite,opal-A,dolomite,pyrite,and rarely calcite and kaolinite Athree-factor model explains the total variaition of major and trace elements in the argillaceous sediments.The first factor is an aluminosilicate factor and involves the following elements:Al,Si,Mg,Na,K,Ti,Mn,Nb,Y,Rb,Zn,Cu,Ni,Cr,Nband V,associated with chlorite,albite and illite.The second factor involves the elements Ca,Sr,Ba,Znand Sc and is related to carbonate lithology and mainly the carbonate concretions with gypsum.The third factor involves Fe and Ce with a weak association with Mn.The diagenesis of the Marathousa sediments and lignites was not very advanced as indicated by (a) the total thickness of the sequence (500m),(b) the presence of biogenic silica(opal-A) and (c) the age of the deposit(Pleistocene).FOr these reasons the rpresence of chlorite,illite and kaolinite in the sediments and lignite is due not to diagenetic reactions but to weathering of the flysch and metamorphic rocks at the edges of the Megalopolis Basin and transport of the weathering products(illite,chlorite,kaolinite)into the basin of deposition.The diagenetic minerals of the Marathousa sequence include pyrite,gypsum,dolomite and aragonite.  相似文献   

11.
INUI  M.; TORIUMI  M. 《Journal of Petrology》2004,45(7):1369-1392
Chemical zoning of garnet is often used to deduce P–Tpaths of rocks by inverse calculation. To validate the derivedP–T paths, it is desired to establish a method to predictthe chemical compositions of garnet theoretically. This studyproposes a new forward calculation of the formation of Mg–Fe–Mngarnet from chlorite, which solves the non-linear simultaneousequations using nested iterative calculations. Growth of garnetconsuming chlorite and quartz was modelled in a MnO–FeO–MgO–Al2O3–SiO2–H2Osystem, using the most recent thermodynamic data for the minerals.The prograde P–T history of the Sambagawa metamorphicbelt, SW Japan, was modelled. To reproduce growth zoning, crystallizedgarnet was removed step by step from the system; perfect diffusionwas assumed for chlorite. The proposed model derived the evolutionof molar amounts and chemical compositions of Mg–Fe–Mnchlorite and garnet. It successfully reproduced the shape ofthe observed chemical profile of garnet, although the temperaturecondition was higher than general observations. The Mn contentof the garnet core was generally high, and Mg/Fe ratio alwaysstarted rising rapidly after Mn was depleted. Thermodynamicproperties of minerals, initial chlorite composition, P–Tpath, H2O partial pressure, and Ca content in garnet were variedto test the behaviour of the system. The properties of Mn phasesinfluenced only the chemical composition of the garnet core.The temperature range in which garnet grew depended on the H2Opartial pressure or the Ca content in garnet. KEY WORDS: chemical equilibrium; chemical zoning; garnet; forward modelling; Sambagawa metamorphic belt  相似文献   

12.
WATERS  D. J. 《Journal of Petrology》1986,27(2):541-565
Sapphirine occurs with cordierite, phlogopite, spinel, sillimanite,corundum, orthopyroxene, and gedrite in granulite facies Mg-and Al-rich paragneisses within the low P, high T NamaqualandMetamorphic Complex. The gneisses reveal a three-stage texturalhistory. Sapphirine appeared during a second stage of progrademineral growth which produced nodular structures and intergrowthsinvolving spinel, corundum, and sillimanite, pseudomorphingan earlier generation of coarse, amphibolite facies minerals.A third generation of coarse, cross-cutting, mainly hydrousminerals (gedrite, kornerupine, phlogopite) is sporadicallydeveloped. The wide variety of cofacial mineral assemblages allows thedelineation of the stable mineral associations of sapphirinein the system K2O-MgO-FeO-Al2O3-SiO2-H2O under P-T conditionsindependently estimated at about 5 kb, 750–800 °C.The natural assemblages provide constraints which, taken togetherwith existing thermodynamic and experimental data, allow theestimation of P-T slopes of sapphirine equilibria. The mineraltextures thus indicate sapphirine growth under increasing T,decreasing a(H2O), and constant or slightly increasing P. The preservation of prograde reaction textures during fine-grainedmineral growth probably results from the reduced importanceand/or more CO2-rich composition of the metamorphic fluid undergranulite facies conditions in these refractory rocks. Aqueousfluids were locally reintroduced after the metamorphic peak.  相似文献   

13.
Peak metamorphism (800–850°C, 8–10 kbar) inthe Harts Range Meta-Igneous Complex (Harts Range, central Australia)was associated with localized partial melting by the reactionhornblende + plagioclase + quartz + H2O = garnet + clinopyroxene+ titanite + melt. In situ trace-element determinations of prograde,peak and retrograde minerals in migmatitic metabasites and associatedtonalitic melts using laser-ablation ICP–MS has allowedmonitoring of a range of partial-melting processes (melting,melt segregation and back-reaction between crystallizing meltand restitic minerals). Mass balance calculations indicate thattitanite is a major carrier of trace elements such as Ti, Nb,Ta, Sm, U and Th, and therefore may be an important accessoryphase to control the redistribution of these elements duringthe partial melting of amphibolites. Titanite preferentiallyincorporates Ta over Nb and, hence, residual titanite mightassist in the formation of melts with high Nb/Ta. The fact thatsingle minerals record different rare earth element (REE) patterns,from prograde to peak to retrograde conditions, demonstratesthat REE diffusion is not significant up to 800°C. Therefore,trace-element analysis in minerals can be a powerful tool toinvestigate high-grade metamorphic processes beyond the limitsgiven by major elements. KEY WORDS: Harts Range; laser-ablation ICP–MS; metabasites; partial melting; trace elements  相似文献   

14.
High-pressure metamorphic rocks form a coastal belt, 175 kmby 35 km, in northeastern New Caledonia. Metamorphic grade rangesfrom lawsonite-albite schists through glaucophane-epidote schiststo omphacite-garnet-quartz gneisses. In the eclogitic terrane,metabasites, locally containing relict pillow structure andigneous textures, with well-preserved eclogitic mineral assemblages,are intercalated with metasedimentary gneisses containing albite-epidote-garnet? glaucophane and barroisite. Omphacite is partly retrogressedto albite and ferromagnesian minerals in almost every paragneiss.The paragneisses show strong evidence of penetrative foldingand microfracturing and were more permeable to metamorphic fluidsthan were the metabasites. The metabasites are inferred to havebeen relatively ‘dry’ and free of penetrative deformationduring the latter stages of metamorphism and thus were preservedmetastably during uplift, erosion, and cooling. Fe-Mg exchange thermometry between omphacite and garnet suggeststemperatures between 520 and 600 ?C. Omphacite + quartz (molper cent jadeite = 37–43) does not coexist stably withalbite suggesting minimum pressures near 12 kb at 550 ?C. Remnantsof more jadeite-rich pyroxenes in paragneisses (jd50–60)suggest even higher pressure. The stable coexistence of chloritoidalmandine-quartz in paragneisses suggests relatively H2O-rich fluids werein equilibrium with this assemblage. The widespread stable occurrenceof sphene suggests relatively low fco2 during metamorphism.Late stage healed fractures in quartz contain H2O-rich fluidinclusions with relatively low density isochores. Limited geochronologicdata combined with these petrologic data suggest a fairly rapidinitial rate of uplift followed by a much slower rate of uplift  相似文献   

15.
Electron microprobe analyses are presented for new-formed mineralsfrom a small exposure of semi-schistose Taveyanne Formationof the pumpellyite-actinolite facies near Lo?che, Valais. Comparisonsare drawn with minerals of other low-grade metamorphic areas,especially in southern New Zealand. Sphene shows considerablesubstitution of Ca(Al,Fe)SiO4(OH) for CaTiSiO5. Epidotes aresharply divided into early pistacitic (Ps = 0.28–0.37)and later clinozoisitic varieties (Ps = 0.11–0.19). Pumpellyitesrange from pumpellyite-(Fe) to pumpellyite-(Al) and are generallyless Fe-rich than those of zeolite and prehnite-pumpellyitefacies. Pumpellyite inclusions in albitized plagioclase areparticularly low in Mg. Actinolites are low in A12O3, TiO2,and Na2O, essentially identical compositions being nucleatedon detrital augite, hornblende, and in the matrix. Phengitesare also extremely low in Na2O and TiO2. Chlorites are ripidolites.Albitized clastic plagioclase has the composition An0.7–1.6and albite in clinozoisite-calcite-albite-phengite-chloriteveins An2.1–2.3. Calcites carry minor Mn > Fe ? Mg.New-formed iron oxides are absent, whereas pyrrhotite and minorpyrite occur in one rock, buffering fs2 and indicating low fo2. Ratios Mg: Fe* (Fe* = total Fe) in coexisting chlorites andA1, Na-poor actinolites vary sympathetically both in the Lo?cheand southern New Zealand rocks here considered, giving KD =(Mg/Fe*) actlnolIte/(Mg/Fe*)chlorle = 1.72. Mg/Fe* ratios inpumpellyites tend to vary sympathetically with those of coexistingchlorites and actinolites but are more variable. Substitutionof (Fe, Mg)Si for A12 in phengitic micas and chlorites variessympathetically in the same suites between mafic volcanic andmore pelitic extremes. Various minor elements also behave ina consistent fashion, indicating an encouraging tendency towardsequilibrium. Variable (though small) A12O3 contents of actinolite,Fe: Al ratios in epidotes and pumpellyites, and Mg: Fe* ratiosin phengites, even within a single grain, are evidence of short-rangedisequilibrium; metamorphic equilibration is evidently easierbetween some crystal structures and structural sites than betweenothers. In phase rule analysis of assemblages in such rocks it is commonlynecessary to treat Fe2O3, FeO, and MgO as separate componentsand it may also be necessary to regard CO2 as an inert componentand/or to interpret observed assemblages as of low variance.The presence of the Ca-Al silicates and sphene indicates verylow Xco2 in the metamorphic fluids in all rocks examined exceptan albite-chlorite-calcite-quartz-anatase assemblage. But higherAn in albites than in isofacial and in greenschist facies rocksof southern New Zealand can be ascribed to significantly higherXco2 at Lo?che, especially in the veins, than in New Zealand. Pumpellyite and epidotes of the pumpellyite-actinolite faciestend to be lower in Fe and richer in Al than those of lowergrade facies. Important reactions include those of the formpumpellyite-(Fe3+)+chlorite+quartz+H2=pumpellyite-(Al)+actinolite,and pumpellyite+chlorite+quartz- ‘epidote’+actinolite+water.Careful selection of pumpellyite and chlorite compositions isrequired for experimental and chemographic analysis of pumpellyitestability. In the absence of critical data, temperatures ofabout 250–350? and pressures of several kilobars are provisionallysuggested for the Lo?che metamorphism.  相似文献   

16.
The petrography and mineralogy of a coarse-grained eclogitelens from the La Rinconada Group of northeastern Margarita Island,Venezuela, reflect the metamorphic evolution of the rock. Omphacite+ garnet + paragonite + barroisite + epidote + rutile/ilmenite+ quartz + pyrite + apatite represents the stable assemblagemarking the culmination of a single metamorphic episode. Electronmicroprobe analyses of the major minerals indicate an affinitywith Smulikowski's low-temperature ‘ophiolitic’type. Schreinemakers relationships among the mineral phasesallow the observed complex reaction relations to be explainedas late-stage depressurization effects. The crystallizationof eclogite instead of amphibole gneiss, as in the chemicallyidentical country rock, must be related to a lower H2O in theaqueous fluid phase attending metamorphism. It is inferred frommineralogical stability data that the ‘culmination assemblage’was stable at approximately 450–525 °C and 11.5–13.5kb load pressure, and that depressurization to less than 5 kboccurred at slightly increasing metamorphic temperatures.  相似文献   

17.
O18/O16 and C12/C13 ratios have been determined for carbonaterocks and coexisting minerals from two contact metamorphic aureolesat Birch Creek, California and Marble Canyon, Texas. The peliticmetasediments and granitic intrusions of the Birth Creek localitywere also analyzed for their O18/16 and D/H ratios. Oxygen andcarbon isotope fractionations in coexisting dolomite and calciteare interrelated but show no obvious correlation with sampledistance from the intrusive contact. Small-scale oxygen isotopicexchange effects between rock units are observed within a fewfeet of the intrusive-country rock contacts and the marble-schistcontacts at Birch Creek. Oxygen isotopic temperatures obtainedfrom quartz—biotite fractionations in the biotite schistsof Birch Creek show a systematic decrease with increasing distanceaway from the intrusive contact; the isotopic contact temperatureis calculated to be 535–45°C. Low O18/16 and C13/12ratiosof the contact metamorphic marbles generally correlate wellwith presence of calc-silicate minerals, indicating that theCO2 liberated during metamorphic decarbonation reactions isenriched in both O18and C12 relative to the carbonates. Materialbalance calculations indicate that the liberated CO2 is about5 per mille richer in O18 and about 6 per mille richer in C13than coexisting calcite.  相似文献   

18.
The Puklen complex of the Mid-Proterozoic Gardar Province, SouthGreenland, consists of various silica-saturated to quartz-bearingsyenites, which are intruded by a peralkaline granite. The primarymafic minerals in the syenites are augite ± olivine +Fe–Ti oxide + amphibole. Ternary feldspar thermometryand phase equilibria among mafic silicates yield T = 950–750°C,aSiO2 = 0·7–1 and an fO2 of 1–3 log unitsbelow the fayalite–magnetite–quartz (FMQ) bufferat 1 kbar. In the granites, the primary mafic minerals are ilmeniteand Li-bearing arfvedsonite, which crystallized at temperaturesbelow 750°C and at fO2 values around the FMQ buffer. Inboth rock types, a secondary post-magmatic assemblage overprintsthe primary magmatic phases. In syenites, primary Ca-bearingminerals are replaced by Na-rich minerals such as aegirine–augiteand albite, resulting in the release of Ca. Accordingly, secondaryminerals include ferro-actinolite, (calcite–siderite)ss,titanite and andradite in equilibrium with the Na-rich minerals.Phase equilibria indicate that formation of these minerals tookplace over a long temperature interval from near-magmatic temperaturesdown to  相似文献   

19.
BUTLER  P.  Jr. 《Journal of Petrology》1969,10(1):56-101
Forty-seven specimens of the Wabush Iron Formation were collectedfrom ten outcrop areas. Twenty-five specimens contain the assemblage(1), quartz+clinopyroxene+calcite with or without orthopyroxene,grunerite, magnetite, ankerite, and siderite. Five specimenscontain assemblage (2), quartz+clinopyroxene+actinolite+calcite+magnetite+hematite,and two contain assemblage (3), quartz+orthopyroxene+actinolite+magnetite+hematite.In three specimens of assemblage (1), graphite occurs in theabsence of magnetite; pyrrhotite and pyrite occur separatelyor together in specimens with assemblage (1). Thirty-nine clinopyroxenes, 38 orthopyroxenes, 18 grunerites,7 actinolites, 16 calcites, 1 ankerite, and 1 siderite wereanalyzed for iron, manganese, and calcium by X-ray emissionspectrography. Magnesium contents were estimated by assumingstoichiometric proportions. Minerals occurring with hematite show low Fe/(Fe+Mg) ratios,and those in the other assemblages show higher values with awide range of variation. In orthopyroxene, Fe/(Fe+ Mg) rangesfrom 0·17 (with hematite) to 0·77. Regularity in the distributions of Fe, Mn, and Ca between pairsof coexisting minerals shows that equilibrium was attained inmost of the rocks studied. This regularity is also accomplishedin the distribution of Mn between calcite and coexisting silicatesas well as between the silicates themselves. Small differencesin the distributions of Ca and Fe depend on both outcrop areaand mineral assemblage. Phase rule considerations suggest that the specimens with dolomite-ankeriteor magnesitesiderite do not represent equilibrium assemblages.Variations in orthopyroxene compositions in assemblages withpyrite or pyrrhotite, or both, and magnetite indicate non-equilibrationof sulfides with silicates. The presence of the oxygen buffer,magnetite+hematite, attests to the immobility of oxygen duringmetamorphism. Within each outcrop area, over which the temperature and pressureare assumed to have been uniform, variations in the compositionsof the silicates in the sub-assemblages quartz+ orthopyroxene+gruneriteand quartz+orthopyroxene+clinopyroxene+calcite indicate gradientsof µH2O µCO2 and respectively. As characterizedby the composition of orthopyroxene, both gradients are relativelylow along strike, and high across strike. The direction of gradientsacross strike is almost without reversals, which is consistentwith intergranular diffusion of H2O and CO2. Phase rule restrictionsfor a majority of assemblages are not in accord with the simultaneousimposition of µH2O and µCO2 gradients on the rocks,nor the formation of an H2O-CO2 fluid phase during metamorphism.  相似文献   

20.
X射线粉晶衍射仪在大理岩鉴定与分类中的应用   总被引：2，自引：2，他引：0  
大理岩主要有方解石大理岩、白云石大理岩和菱镁矿大理岩三种。以往大理岩是依据偏光显微镜下观察岩石结构构造及矿物成分进行分类定名,由于方解石、白云石、菱镁矿都属于三方晶系,具有闪突起、高级白干涉色、一轴晶负光性和菱形解理等相同晶体光学特征,偏光显微镜下区分十分困难。为了准确鉴定大理岩中碳酸盐矿物种类及其相对含量,本文利用岩石薄片偏光显微镜和X射线粉晶衍射技术对32件大理岩岩石样品进行分析测试。岩石薄片鉴定结果表明:大理岩造岩矿物主要有方解石、白云石、菱镁矿、石英、斜长石、白云母、黑云母、绿泥石、黏土和金属矿物。根据岩石结构构造及矿物组分特征,可把32件大理岩样品划分为方解石大理岩、长英质方解石大理岩、石英绿泥白云石大理岩、白云石大理岩、云英质白云石大理岩和菱镁矿大理岩等15个类型。X射线粉晶衍射分析表明:大理岩造岩矿物主要有方解石、白云石、菱镁矿、石英、斜长石、钾长石、云母、绿泥石、滑石和蒙脱石。综合分析认为:岩石薄片偏光显微镜鉴定技术很难区分方解石、白云石和菱镁矿等碳酸盐矿物,以及细小的石英、钾长石和斜长石、滑石和白云母等鳞片状硅酸盐矿物;X射线粉晶衍射分析技术不仅能准确检测出大理岩中方解石、白云石和菱镁矿等碳酸盐矿物种类及相对含量(方解石、白云石和菱镁矿的X射线衍射主峰有明显差异,d值分别为0.303 nm、0.288 nm和0.274 nm),而且能够有效鉴别岩石中粉砂级斜长石、钾长石与石英(三种矿物的X射线衍射主峰d值分别为0.319 nm、0.324 nm、0.334 nm);且能区分蒙脱石、绿泥石、云母和滑石等层状硅酸盐矿物(四种硅酸盐矿物的X射线衍射主峰d值分别为1.400 nm、0.705 nm、0.989 nm、0.938 nm)。综合岩石薄片偏光显微镜鉴定和X射线粉晶衍射分析结果,最终确定32件大理岩样品划分为22个岩石类型。研究认为:仅根据岩石薄片偏光显微镜鉴定或X射线粉晶衍射技术其中一种方法不能准确鉴定大理岩岩石,应将大理岩岩石野外观察、岩石薄片鉴定和X射线粉晶衍射技术结合起来,才能准确确定大理岩岩石类型。  相似文献   

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