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1.
The major element composition of plagioclase, pyroxene, olivine,and magnetite, and whole-rock 87Sr/86Sr data are presented forthe uppermost 2·1 km of the layered mafic rocks (upperMain Zone and Upper Zone) at Bierkraal in the western BushveldComplex. Initial 87Sr/86Sr ratios are near-constant (0·7073± 0·0001) for 24 samples and imply crystallizationfrom a homogeneous magma sheet without major magma rechargeor assimilation. The 2125 m thick section investigated in drillcore comprises 26 magnetitite and six nelsonite (magnetite–ilmenite–apatite)layers and changes up-section from gabbronorite (An72 plagioclase;Mg# 74 clinopyroxene) to magnetite–ilmenite–apatite–fayaliteferrodiorite (An43; Mg# 5 clinopyroxene; Fo1 olivine). The overallfractionation trend is, however, interrupted by reversals characterizedby higher An% of plagioclase, higher Mg# of pyroxene and olivine,and higher V2O5 of magnetite. In the upper half of the successionthere is also the intermittent presence of cumulus olivine andapatite. These reversals in normal fractionation trends definethe bases of at least nine major cycles. We have calculateda plausible composition for the magma from which this entiresuccession formed. Forward fractional crystallization modelingof this composition predicts an initial increase in total iron,near-constant SiO2 and an increasing density of the residualmagma before magnetite crystallizes. After magnetite beginsto crystallize the residual magma shows a near-constant totaliron, an increase in SiO2 and decrease in density. We explainthe observed cyclicity by bottom crystallization. Initiallymagma stratification developed during crystallization of thebasal gabbronorites. Once magnetite began to crystallize, periodicdensity inversion led to mixing with the overlying magma layer,producing mineralogical breaks between fractionation cycles.The magnetitite and nelsonite layers mainly occur within fractionationcycles, not at their bases. In at least two cases, crystallizationof thick magnetitite layers may have lowered the density ofthe basal layer of melt dramatically, and triggered the proposeddensity inversion, resulting in close, but not perfect, coincidenceof mineralogical breaks and packages of magnetitite layers. KEY WORDS: layered intrusion; mineral chemistry; isotopes; magma; convection; differentiation  相似文献   

2.
The Kap Edvard Holm Layered Gabbro Complex is a large layeredgabbro intrusion (>300 km2) situated on the opposite sideof the Kangerdlugssuaq fjord from the Skaergaard Intrusion.It was emplaced in a continental margin ophiolite setting duringearly Tertiary rifting of the North Atlantic. Gabbroic cumulates, covering a total stratigraphic thicknessof >5 km, have a typical four-phase tholeiitic cumulus mineralogy:plagioclase, clinopyroxene, olivine, and Fe–Ti oxides.The cryptic variation is restricted (plagioclase An81–51,olivine Fo85–66, clinopyroxene Wo43–41 En46–37Fs20–11) and there are several reversals in mineral chemistry.Crystallization took place in a low-pressure, continuously fractionatingmagma chamber system which was periodically replenished andtapped. Fine-grained (0•2–0•4 mm) equigranular, thin(0•5–3 m), laterally continuous basaltic zones occurwithin an {small tilde}1000 m thick layered sequence in theTaco Point area. Twelve such zones define the bases of individualmacrorhythmic units with an average thickness of {small tilde}80m. The fine-grained basaltic zones grade upwards, over a fewmetres, into medium-grained (>1 mm) poikilitic, olivine gabbrowith smallscale modal layering. Each fine-grained basaltic zoneis interpreted as an intraplutonic quench zone in which magmachilled against the underlying layered gabbros during influxalong the chamber floor. Supercooling by {small tilde}50C isbelieved to have caused nucleation of plagioclase, olivine,and clinopyroxene in the quench zone. The nucleation rate isbelieved to have been enhanced as the result of in situ crystallizationin a continuously flowing magma. The transition to the overlyingpoikilitic olivine gabbro reflects a decreasing degree of supercooling. Compositional variation in the Taco Point sequence is typicalfor an open magma chamber system: olivine (Fo77–68 5)and plagioclase cores (An80–72) show a zig-zag crypticvariation pattern with no overall systematic trend. Olivinehas the most primitive compositions in the quench zones andmore evolved compositions in the olivine gabbro; plagioclasecores show the opposite trend. Although plagioclase cores arebelieved to retain their original compositions, olivines re-equilibratedby reaction with trapped liquid. Some plagioclase cores containrelatively sodic patches which retain quench compositions. Whole-rock compositions of nine different quench zones varyover a range from 10 to 18% MgO although the mg-number remainsconstant at {small tilde}0•78. The average composition(47•7% SiO2, 13•3%MgO, 1•57% Na2O+K2O) is takenas a best estimate of the parental magma composition, and isequivalent to a high-magnesian olivine tholeiite. The compositionalvariation of the quench zones is believed to reflect burstsof nucleation and growth of olivine and plagioclase during quenching. Magma emplacement is believed to have taken place by separatetranquil influxes which flowed along the interface between alargely consolidated cumulus pile and the residual magma. Theresident magma was elevated with little or no mixing. At certainlevels in the layered sequence the magma drained back into thefeeder system; such a mechanism is referred to as a surge-typemagma chamber system.  相似文献   

3.
Blue Mountain is a central-type alkali ultrabasic-gabbro ringcomplex (lxl7middot;5 km) introducing Upper Jurassic sediments,Marlborough, New Zealand. The ultrabasic-gabbroic rocks containlenses of kaersutite pegmatite and sodic syenite pegmatite andare intruded by ring dykes of titanaugite-ilmenite gabbro andlamprophyre. The margin of the intrusion is defined by a ringdyke of alkali gabbro. The plutonic rocks are cut by a swarmof hornblendebiotite-rich lamprophyre dykes. Thermal metamorphismhas converted the sediments to a hornfels ranging in grade fromthe albite-epidote hornfels facies to the upper limit of thehornblende hornfels facies. The rocks are nepheline normative and consist of olivine (Fo82–74),endiopside (Ca45Mg48Fe7–Ca36Mg55Fe9), titanaugite (Ca40Mg50Fe10–Ca44Mg39Fe17),plagioclase (An73–18), and ilmenitetitaniferous magnetite,with various amounts of titaniferous hornblende and titanbiotite.There is a complete gradation between endiopside and titanaugitewith the coupled substitution Ry+2+Si;;(Ti+4+Fe+3+Al+3 and asympathetic increase in CaAl2SiO6 (0·2–10·2percent) and CaTiAl2O6 (2·1–8·1 per cent)with fractionation. Endiopside shows a small, progressive Mgenrichment along a trend subparallel to the CaMgSi2O6–Mg2Si2O6boundary, and titanaugite is enriched in Ca and Fe+2+Fe+3 withdifferentiation. Oscillatory zoning between endiopside and titanaugiteis common. Exsolved ilmenite needles occur in the most Fe-richtitanaugites. The amphiboles show the trend: titaniferous hornblende(1·0–57middot;7 per cent TiO2) kaersutite (6·4per cent TiO2) Fe-rich hastingsite (18·0–19·1per cent FeO as total Fe). Biotite is high in TiO2 (6·6–7·8per cent). Ilmenite and titaniferous magnetite (3·5–10·6per cent TiO2) are typically homogeneous grains; their compositioncan be expressed in terms of R+2RO3:R+2O:R2+3O4. The intrusion of igneous rocks was probably controlled by subterraneanring fracturing. Subsidence of the country rock within the ringfracture provided space for periodic injections of magma froma lower reservoir up the initial ring fracture to form the BlueMountain rocks at a higher level. Downward movement of the floorof the intrusion during crystallization caused inward slumpingof the cumulates which affected the textural, mineralogical,and chemical evolution of the rocks in different parts of theintrusion. The order of mineral fractionation is reflected by the chemicalvariation in the in situ ultrabasic-gabbroic rocks and the successiveintrusions of titanaugite-ilmenite gabbro and lamprophyre ringdykes, marginal alkali gabbro and lamprophyre dyke swarm. Aninitial decrease, then increase in SiO2; a steady decrease inMgO, CaO, Ni, and Cr: an initial increase, then decrease inFeO+Fe2O3, TiO2, MnO, and V; almost linear increase in A12O3and late stage increase in alkalis and P2O3, implies fractionationof olivine and endiopside, followed by titanaugite and Fe-Tioxides, followed by plagioclase, hornblende, biotite, and apatite.Reversals in the composition of cumulus olivine and endiopsideand Solidification Index, indicate that the ultrabasic-gabbroicsequence is composed of four main injections of magma. The ultrabasic rocks crystallized under conditions of high PH2Oand fairly high, constant  相似文献   

4.
The early augite syenite unit in the 1·13-Ga-old Ilímaussaqintrusive complex, South Greenland, consists of a magmatic assemblageof ternary alkali feldspar + fayalitic olivine + augite + titanomagnetite+ apatite + baddeleyite ± nepheline ± quartz ±ilmenite ± zircon. Feldspar, nepheline and QUILF thermometryyield T = 1000–700°C, at P = 1 kbar, which is derivedfrom fluid inclusion data from other parts of the complex. Ternaryfeldspar was the first major liquidus phase. It crystallizedat temperatures between 950 and 1000°C from a homogeneousmagma with aSiO2 = 0·8 and fO2 about 1·5–2log units below the fayalite–magnetite–quartz (FMQ)buffer. Later, closed system fractionation produced nepheline-bearingassemblages with aSiO2 = 0·4 and log fO2 = FMQ –3 to FMQ – 5. Assimilation of wall rocks produced localvariations of melt composition. Four traverses through the unitwere sampled parallel to the assumed direction of crystallization.They exhibit significant differences in their mineral assemblagesand compositions. The chemical zoning and calculated intensiveparameters of four sample suites reflect both closed systemfractional crystallization and local assimilation of wall rocks. KEY WORDS: alkaline magmatism; assimilation; fractionation; redox equilibria; QUILF  相似文献   

5.
The alpine-type peridotite at Burro Mountain is a partiallyserpentinized harzburgite-dunite body approximately 2 km indiameter. It lies in a chaotic mélange derived from theFranciscan Formation (Upper Jurassic to Upper Cretaceous) ofthe southern Coast Ranges of California. The peridotite is boundedon the east by a vertical fault in the Nacimiento fault zonethat brings sedimentary rocks of Taliaferro's (1943b) AsuncionGroup (Upper Cretaceous) into contact with the peridotite. Theperidotite appears to be one of a number of tectonic lenses,having a wide range in size, that make up the mélange.These lenses include metagraywacke, metachert, greenstone, amphibolite,and blueschist, as well as ultramafic rocks, and represent awide range of pressure-temperature environments. The outer shell of the peridotite is a sheared serpentinitezone 10–15 m thick. The peridotite was tectonically emplacedat its present level as a cold solid mass and had little effecton the mineral assemblages of the Franciscan Formation. Localdevelopment of lawsonite and aragonite in shear zones may berelated to the peridotite emplacement. Foliated harzburgite forms approximately 60 per cent of theperidotite. It is a lithologically uniform rock that has anolivine: orthopyroxene ratio of approximately 75:25. Accessoryclinopyroxene and chromian spinel generally make up less than5 per cent of the harzburgite. Dunite, composed of olivine,accessory chromian spinel (< 5 per cent), and trace amountsof pyroxene, makes up approximately 40 per cent of the peridotiteand occurs as dikes, sills, and irregular bodies in the harzburgite. Olivine and pyroxene show small but significant compositionalvariations and chromian spinel shows a large range in the cationratio Cr/(Cr+Al+ Fe3+). The compositional variations in theseminerals are related to original differences in bulk chemicalcomposition. The following compositional ranges were determinedfor minerals in the harzburgite: olivine, Fo91.1–Fo91.4;orthopyroxene, En89.8–En91.1; clinopyroxene, Ca47.0Mg50.0Fe3.0–Ca48.7Mg48.2Fe3.1;chromian spinel, Cr/(Cr+Al+Fe3+) 0.37–0.55. The pyroxeneshave a range in A12O3 content of 1.3–3.0 wt per cent.Olivine from dunite ranges from Fo91 to Fo92 7 and the chromianspinel has a range in the Cr/(Cr+Al+Fe3+) ratio of 0.30–0.75.Although all the dunites are lithologically similar, three distincttypes are recognized on the basis of composition of coexistingolivine and chromian spinel. Structural relations between thethree types of dunite suggest three periods of emplacement (possiblyoverlapping) of dunite into harzburgite. The evidence indicatesthat the dunite, and probably also the harzburgite crystallizedfrom an ultramafic magma, probably in the upper mantle. After the magmatic episode and crystallization, the peridotitewas subjected to a deep-seated plastic deformation and recrystallization.The first phase of the deformation produced a pervasive, planarstructural element (S1) that crosscuts many harzburgite-dunitecontacts. It is probable that some of the dunite sills wereemplaced during this deformation. The foliation, S1, is definedby layers of different orthopyroxene content in harzburgite,and by discontinuous layers of chromian spinel in dunite. Flowor slip along S1 produced slip folds in harzburgite—dunitecontacts with axial planes parallel to S1. At a later stage,isoclinal folds developed in S1, and the present olivine microfabricwas probably formed by recrystallization in the stress fieldthat produced the isoclinal folding. In the olivine microfabric,X tends to be perpendicular to the axial planes (S2) of theisoclinal folds and Y and Z tend to form double maxima in S2approximately 90° apart. Mg–Fe2+ distribution betweencoexisting mineral pairs yields a calculated temperature offormation of approximately 1200 °C. Although this temperatureis only a nominal value, it indicates that the mineral pairsequilibrated at a significantly high temperature. In view ofthe deformation and recrystallization, the calculated temperaturepossibly represents subsolidus re-equilibration of the mineralsduring this event. The deformation and recrystallization probablyoccurred shortly after crystallization while the peridotitewas still at a high temperature. A later deep-seated deformation produced small scattered kinkfolds in S1 that tend to disrupt the major olivine microfabric.The kink folding was accompanied or followed by the developmentof kink bands in olivine that reflect intragranular glidingon the system T = [Okl], t = [100]. The kink bands probablyformed at a minimum temperature of 1000 °C. Following the deep-seated deformation, which probably took placein the mantle, the peridotite mass was tectonically detachedand moved upward to its present level in the crust. Cleavages,joints, and faults provided channels for water to pervade theperidotite and allow alteration of the primary minerals.  相似文献   

6.
Pelitic xenoliths derived from amphibolite grade basement rocksoccur within a Pleistocene, trachytic, pyroclastic unit of theWehr volcano, East Eifel, West Germany: With increasing temperatureand/or prolonged heating at high temperature, quartz-plagioclaseand micaceous layers of the xenoliths have undergone meltingto form buchites and thermal reconstitution by dehydration reactions,melting and crystallization to form restites respectively. Thexenoliths provide detailed evidence of melting, high temperaturedecomposition of minerals, nucleation and growth of new phasesand P-T-fo2 conditions of contact metamorphism of basement rocksby the Wehr magma. Melting begins at quartz-oligoclase (An17·3Ab82·3Or0·4-An20·0Ab78·1Or1·9)grain boundaries in quartz-plagioclase rich layers and the amountof melting is controlled by H2O and alkalis released duringdehydroxylation/oxidation of associated micas. Initially, glasscompositions are heterogeneous, but with increasing degreesof melting they become more homogeneous and are similar to S-typegranitic minimum melts with SiO2 between 71 and 77 wt. per cent;A/(CNK) ratios of 1·2–1·4; Na2O < 2·95and normative corundum contents of 1·9–4·0per cent. Near micas plagioclase melts by preferential dissolutionof the NaAlSi3O8 component accompanied by a simultaneous increasein CaAl2Si2O8 (up to 20 mol. per cent An higher than the bulkplagioclase composition) at the melting edge. With increasingtemperature the end product of fractional melting is the formationand persistence of refractory bytownite (An78–80) in thosexenoliths where extensive melting has taken place. Initial stage decomposition of muscovite involves dehydroxylation(H2O and alkali loss). At higher temperatures muscovite breaksdown to mullite, sillimanite, corundum, sanidine and a peraluminousmelt. Mullite (40–43 mol. per cent SiO2) and sillimanite(49 mol. per cent SiO2) are Fe2O3 and TiO2 rich (up to 6·1–0·84and 3·6–0·24 wt. per cent respectively).Al-rich mullite (up to 77 wt. per cent Al2O3) occurs with corundumwhich has high Fe2O3 and TiO2 (up to 6·9 and 2·1wt. per cent respectively). Annealing at high temperatures andreducing conditions results in the exsolution of mullite fromsillimanite and ilmenite from corundum. Glass resulting fromthe melting of muscovite in the presence of quartz is peraluminous(A/(CNK) = 1·3) with SiO2 contents of 66–69 percent and normative corundum of 4 per cent. Sanidine (An1·9Ab26·0Or72·1-An1·3Ab15·9Or82·9)crystallized from the melt. Dehydroxylation and oxidation of biotite results in a decreaseof K2O from 8·6 to less than 1 wt. per cent and oxidetotals (less H2O + contents) from 96·5 to 88·6,exsolution of Al-magnetite, and a decrease in the Fe/(Fe + Mg)ratio from 0·41 to 0·17. Partial melting of biotitein the presence of quartz/plagioclase to pleonaste, Al-Ti magnetite,sanidine(An2·0Ab34·9Or63·1) and melt takesplace at higher temperatures. Glass in the vicinity of meltedbiotite is pale brown and highly peraluminous (A/CNK = 2·1)with up to 6 wt. per cent MgO+FeO(total iroq) and up to 10 percent normative corundum. Near liquidus biotite with higher Al2O3and TiO2 than partially melted biotite crystallized from themelt. Ti-rich biotites (up to 6 wt. per cent TiO2) occur withinthe restite layers of thermally reconstituted xenoliths. Meltingof Ti-rich biotite and sillimanite in contact with the siliceousmelt of the buchite parts of xenoliths resulted in the formationof cordierite (100 Mg/(Mg+Fe+Mn) = 76·5–69·4),Al-Ti magnetite and sanidine, and development of cordierite/quartzintergrowths into the buchite melt. Growth of sanidine enclosedrelic Ca-plagioclase to form patchy intergrowths in the restitelayers. Cordierite (100 Mg/(Mg+Fe+Mn) = 64–69), quartz,sillimanite, mullite, magnetite and ilmenite, crystallized fromthe peraluminous buchite melt. Green-brown spinels of the pleonaste-magnetite series have awide compositional variation of (mol. per cent) FeAl2O4—66·6–45·0;MgAl2O4—53·0–18·7; Fe3O4—6·9–28·1;MnAl2O4—1·2–1·5; Fe2TiO4—0·6–6·2.Rims are generally enriched in the Fe3O4 component as a resultof oxidation. Compositions of ilmenite and magnetite (single,homogeneous and composite grains) are highly variable and resultfrom varying degrees of high temperature oxidation that is associatedwith dehydroxylation of micas and melting. Oxidation mainlyresults in increasing Fe3+, Al and decreasing Ti4+, Fe2+ inilmenite, and increasing Fe2+, Ti4+ and decreasing Fe3+ in associatedmagnetite. A higher degree of oxidation is reached with exsolutionof rutile from ilmenite and formation of titanhematite and withexsolution of pleonaste from magnetite. Ti-Al rich magnetite(5·1–7·5 and 8·5–13·5wt. per cent respectively) and ilmenite crystallized from meltsin buchitic parts of the xenoliths. Chemical and mineralogic evidence indicates that even with extensivemelting the primary compositions of individual layers in thexenoliths remained unmodified. Apparently the xenoliths didnot remain long enough at high temperatures for desilicationand enrichment in Al2O3, TiO2, FeO, Fe2O3, and MgO that resultsby removal of a ‘granitic’ melt, and/or by interactionwith the magma, to occur. T °C-fo2 values calculated from unoxidized magnetite/ilmenitegive temperatures ranging from 615–710°C for contactmetamorphism and the beginning of melting, and between 873 and1054°C for the crystallization of oxides and mullite/sillimanitefrom high temperature peraluminous melts. fo2 values of metamorphismand melting were between the Ni-NiO and Fe2O3-Fe3O4 buffer curves.The relative abundance of xenolith types, geophysical evidenceand contact metamorphic mineralogy indicates that the xenolithswere derived from depths corresponding to between 2–3kb Pload = Pfluid. The xenoliths were erupted during the latestphreatomagmatic eruption from the Wehr volcano which resultedin vesiculation of melts in partially molten xenoliths causingfragmentation and disorientation of solid restite layers.  相似文献   

7.
Blue Mountain is a central-type alkali ultrabasic-gabbro ringcomplex (1?1?5 km) introducing Upper Jurassic sediments, Marlborough,New Zealand. The ultrabasic-gabbroic rocks contain lenses ofkaersutite pegmatite and sodic syenite pegmatite and are intrudedby ring dykes of titanaugite-ilmenite gabbro and lamprophyre.The margin of the intrusion is defined by a ring dyke of alkaligabbro. The plutonic rocks are cut by a swarm of hornblende-biotite-richlamprophyre dykes. Thermal metamorphism has converted the sedimentsto a hornfels ranging in grade from the albite-epidote hornfelsfacies to the upper limit of the hornblende hornfels facies. The rocks are nepheline normative and consist of olivine (Fo82-74),endiopside (Ca45Mg48Fe7-Ca36Mg55Fe9), titanaugite (Ca40Mg50Fe10-Ca44Mg39Fe17),plagioclase (An73-18), and ilmenitetitaniferous magnetite, withvarious amounts of titaniferous hornblende and titanbiotite.There is a complete gradation between end-iopside and titanaugitewith the coupled substitution Ry+z+Si(Ti+4+Fe+3)+Al+3 and asympathetic increase in CaAl2SiO6 (0?2-10?2 percent) and CaTiAl2O6(2?1-8?1 per cent) with fractionation. Endiopside shows a small,progressive Mg enrichment along a trend subparallel to the CaMgSi2O6-Mg2Si2O6boundary, and titanaugite is enriched in Ca and Fe+2+Fe+3 withdifferentiation. Oscillatory zoning between endiopside and titanaugiteis common. Exsolved ilmenite needles occur in the most Fe-richtitanaugites. The amphiboles show the trend: titaniferous hornblende(1?0–5?7 per cent TiO2)kaersutite (6?4 per cent TiO2)Fe-richhastingsite (18?0–19?1 per cent FeO as total Fe). Biotiteis high in TiO2 (6?6–7?8 per cent). Ilmenite and titaniferousmagnetite (3?5–10?6 per cent TiO2) are typically homogeneousgrains; their composition can be expressed in terms of R+2RO3:R+2O:R2+3O4. The intrusion of igneous rocks was probably controlled by subterraneanring fracturing. Subsidence of the country rock within the ringfracture provided space for periodic injections of magma froma lower reservoir up the initial ring fracture to form the BlueMountain rocks at a higher level. Downward movement of the floorof the intrusion during crystallization caused inward slumpingof the cumulates which affected the textural, mineralogical,and chemical evolution of the rocks in different parts of theintrusion. The order of mineral fractionation is reflected by the chemicalvariation in the in situ ultrabasic-gabbroic rocks and the successiveintrusions of titanaugite-ilmenite gabbro and lamprophyre ringdykes, marginal alkali gabbro and lamprophyre dyke swarm. Aninitial decrease, then increase in SiO2; a steady decrease inMgO, CaO, Ni, and Cr: an initial increase, then decrease inFeO+Fe2O3, TiO2, MnO, and V; almost linear increase in Al2O3and late stage increase in alkalis and P2O3, implies fractionationof olivine and endiopside, followed by titanaugite and Fe-Tioxides, followed by plagioclase, hornblende, biotite, and apatite.Reversals in the composition of cumulus olivine and endiopsideand Solidification Index, indicate that the ultrabasic-gabbroicsequence is composed of four main injections of magma. The ultrabasic rocks crystallized under conditions of high PH2Oand fairly high, constant PO2; PH2 and PO2 increased duringthe formation of the gabbroic rocks until fracturing of thechamber roof occurred. The abundance of euhedral amphibole inthe latter injection phases suggests that amphibole accumulatedfrom a hydrous SiO2 undersaturated magma when an increase inPO2, stabilized its crystallization. Plutonic complexes similar to Blue Mountain are found withinand beneath the volcanic piles of many oceanic islands, e.g.Canaries, Reunion, and Tahiti, and those intruding thick sedimentarysequences, as at Blue Mountain, e.g. the pipe-like intrusionsof the Monteregian Hills, Quebec.  相似文献   

8.
The ejected blocks of the Soufrière volcano consist ofthe mineral phases anorthite (An96-An89; average An93), olivine(Fo79-Fo67; most frequent interval Fo74-71), salite con taining5–6 per cent Al2, O3, hastingsitic amphibole, and magnetitecontaining 6 per cent A12O3, 4 per cent MgO, 7 per cent TiO2.The minerals occur in various proportions and textures. Theyare virtually unzoned and represent material which has beenejected at, and quenched from, a high temperature. The interstitialscoria present among the mineral grains in the blocks has thecomposition of a saturated sub-alkaline aluminous basalt, andis believed to represent the liquid phase with which the mineralswere in equilibrium at depth. The high-temperature mineralogy,the textures and structures of the rocks support the view thatthe blocks represent crystal cumulates which have crystallizedunder high water-vapor pressures from a fractionating basaltmagma at a depth approximating 6 km. The bulk composition ofthe blocks is such that the resultant liquid fractions are enrichedin silica. Fractional crystallization may be an important factorin the evolution of some calc-alkaline suites.  相似文献   

9.
Using experimental results at 1·0 GPa for the systemsCaO–SiO2, MgO–SiO2, CaMgSi2O6–SiO2 and CaMgSi2O6–Mg2SiO4,and all the currently available phase equilibria and thermodynamicdata at 1 bar, we have optimized the thermodynamic propertiesof the liquid phase at 1·0 GPa. The new optimized thermodynamicparameters indicate that pressure has little effect on the topologyof the CaO–SiO2, CaMgSi2O6–SiO2, and CaMgSi2O6–Mg2SiO4systems but a pronounced one on the MgO–SiO2 binary. Themost striking change concerns passage of the MgSiO3 phase fromperitectic melting at 1 bar to eutectic melting at 1·0GPa. This transition is estimated to occur at 0·41 GPa.For the CaMgSi2O6–SiO2 and CaMgSi2O6–Mg2SiO4 pseudo-binaries,the size of the field clinopyroxene + liquid increases withincreasing pressure. This change is related to the shift ofthe piercing points clinopyroxene + silica + liquid (from 0·375mol fraction SiO2 at 1 bar to 0·414 at 1·0 GPa)and clinopyroxene + olivine + liquid (from 0·191 molfraction SiO2 at 1 bar to 0·331 at 1·0 GPa) thatbound the clinopyroxene + liquid field in the CaMgSi2O6·SiO2and CaMgSi2O6·Mg2SiO4 pseudo-binaries, respectively. KEY WORDS: CaO–SiO2; CaMgSi2O6–Mg2SiO4; CaMgSi2O6–SiO2; experiments; MgO–SiO2  相似文献   

10.
A 525-m-long drill core (DDH-221) through the Partridge Riverintrusion has been divided into four zones on the basis of changesin mineral abundances, compositions and grain size. The igneousrocks in the core consist of cumulate gabbro, troctolite andolivine gabbronorite, in which the original cumulate frameworkof plagioclase and olivine contained varying amounts of trappedintercumulus (pore) liquid. The compositions of the unzoned olivine (Fo31–71) havebeen modified by reaction with Fe-rich in situ intercumulusliquid, but the plagioclase cores (An59–73) have not.The compositions of postcumulus Ca-rich pyroxene, restrictedto En36–44, and the more variable Ca-poor pyroxene (En45–74),follow a downward Fe-enrichment trend similar to the Fe-enrichmentin the olivine. The cumulus olivine expected to be in equilibriumwith plausible parental magmas to these rocks was not preservedin the drill core, nor is the chilled margin to the intrusionsufficiently primitive to account for all the olivine. Revisedmass balance estimates of the primary magmatic compositionsof olivine are Fo67–85. The new limiting value for theprimary olivine is similar to the Fo83–85 olivine expectedto crystallize from the chilled margin to the nearby PigeonPoint olivine diabase sill under equilibrium conditions. Thechanges in the mineral compositions in core DDH-221 do not adequatelydescribe the behavior of parental melts on an equilibrium coolingpath, implying that the cumulus plagioclase and olivine crystallizedelsewhere, and were mixed with varying amounts of intercumulusliquid before introduction to the present crustal site of thePartridge River intrusion. Rock density increases with depth from 2?76 to 3?21, with amean of 2?98 g/cm3. Estimated trapped liquid densities rangefrom 2?56 to 2?92 g/cm3 at high temperatures. This is interpretedto mean that the intercumulus liquid could not have been expelledupward by compaction of the cumulate pile. The dense intercumulusliquid increased downward in abundance to form a series of rocksthat range continuously from variously packed framework cumulatesto chilled non-cumulate rocks in the basal zone. In situ crystallizationis concluded to be the dominant mode of solidification of thePartridge River intrusion, in which infiltration metasomatismis precluded by the high liquid density.  相似文献   

11.
Experimental Melting of Carbonated Peridotite at 6-10 GPa   总被引：2，自引：0，他引：2  
Partial melting of magnesite-bearing peridotites was studiedat 6–10 GPa and 1300–1700°C. Experiments wereperformed in a multianvil apparatus using natural mineral mixesas starting material placed into olivine containers and sealedin Pt capsules. Partial melts originated within the peridotitelayer, migrated outside the olivine container and formed poolsof quenched melts along the wall of the Pt capsule. This allowedthe analysis of even small melt fractions. Iron loss was nota problem, because the platinum near the olivine container becamesaturated in Fe as a result of the reaction Fe2SiO4Ol = FeFe–Ptalloy + FeSiO3Opx + O2. This reaction led to a gradual increasein oxygen fugacity within the capsules as expressed, for example,in high Fe3+ in garnet. Carbonatitic to kimberlite-like meltswere obtained that coexist with olivine + orthopyroxene + garnet± clinopyroxene ± magnesite depending on P–Tconditions. Kinetic experiments and a comparison of the chemistryof phases occasionally grown within the melt pools with thosein the residual peridotite allowed us to conclude that the meltshad approached equilibrium with peridotite. Melts in equilibriumwith a magnesite-bearing garnet lherzolite are rich in CaO (20–25wt %) at all pressures and show rather low MgO and SiO2 contents(20 and 10 wt %, respectively). Melts in equilibrium with amagnesite-bearing garnet harzburgite are richer in SiO2 andMgO. The contents of these oxides increase with temperature,whereas the CaO content becomes lower. Melts from magnesite-freeexperiments are richer in SiO2, but remain silicocarbonatitic.Partitioning of trace elements between melt and garnet was studiedin several experiments at 6 and 10 GPa. The melts are very richin incompatible elements, including large ion lithophile elements(LILE), Nb, Ta and light rare earth elements. Relative to theresidual peridotite, the melts show no significant depletionin high field strength elements over LILE. We conclude fromthe major and trace element characteristics of our experimentalmelts that primitive kimberlites cannot be a direct productof single-stage melting of an asthenospheric mantle. They rathermust be derived from a previously depleted and re-enriched mantleperidotite. KEY WORDS: multianvil; carbonatite melt; peridotite; kimberlite; element partitioning  相似文献   

12.
The 150 m thick late Miocene Graveyard Point sill (GPS) is situated at the Idaho-Oregon border near the southwestern edge of the western Snake River Plain. It records from bottom to top continuous fractional crystallization of a tholeiitic parent magma (lower chilled border, FeO/(FeO+MgO) = 0.59, Ni = 90 ppm) towards granophyres (late pods and dikes, FeO/(FeO+MgO) = 0.98, 78 wt% SiO2 3.5 wt% K2O, <4 ppm Ni) showing a typical trend of Fe and P enrichment. Fractionating minerals are olivine (Fo79-Fo2), augite (X Fe = 0.18−0.95), feldspars (An80Or1-An1Or62), Fe-Ti oxides (Ti-rich magnetite and ilmenite), apatite and in two samples super-calcic pigeonite (Wo18–28 Fs41–54). The granophyres may bear some quartz. Compositionally zoned minerals record a large interval of the fractionation process in every single sample, but this interval changes with stratigraphic height. In super-calcic pigeonite-bearing samples, olivine is scarce or lacking and because super-calcic pigeonite occurs as characteristic overgrowths on augite, its formation is interpreted to be related to the schematic reaction: augite + olivine (component in melt) + SiO2 (in melt) = pigeonite, that defines the cotectic between augite and pigeonite in olivine-saturated basaltic systems. Line measurements with the electron microprobe reveal that the transition from augite to super-calcic pigeonite is continuous. However, some crystals show an abrupt “reversal” towards augite after super-calcic pigeonite growth. Two processes compete with each other in the GPS: fractional crystallization of the bulk liquid (the bulk melt separates from solids and interstitial liquids in the solidification front) and fractional crystallization of interstitial melt in the solidification front itself. Interplay between those two processes is proposed to account for the observed variations in mineral chemistry and mineral textures. Received: 25 November 1998 / Accepted: 14 June 1999  相似文献   

13.
Alaskan-type platinum-bearing plutons and potassium-enrichedmafic to ultramafic volcanic rocks are temporally and spatiallyassociated within the Late Cretaceous–Paleocene Achaivayam–Valaginskiiintra-oceanic palaeo-arc system, allochthonously present inthe Koryak Highland and Kamchatka Peninsula (Far East Russia).The compositions of the parental magmas to the Alaskan-typecomplexes are estimated using the Galmoenan plutonic complexas an example. This complex, composed of dunites, pyroxenitesand minor gabbros, is the largest (20 km3) in the system andthe best studied owing to associated platinum placer deposits.The compositions of the principal mineral phases in the Galmoenanintrusive rocks [olivine (Fo79–92), clinopyroxene (1–3·5wt % Al2O3, 0·1–0·5 wt % TiO2), and Cr-spinel(5–15 wt % Al2O3 and 0·3–0·7 wt %TiO2)] are typical of liquidus assemblages in primitive island-arcmagmas in intra-oceanic settings, and closely resemble the mineralcompositions in the Achaivayam–Valaginskii ultramaficvolcanic rocks. The temporal and spatial association of intrusiveand extrusive units, and the similarity of their mineral compositions,suggest that both suites were formed from similar parental magmas.The composition of the parental magma for the Galmoenan plutonicrocks is estimated using previously reported data for the Achaivayam–Valaginskiiultramafic volcanic rocks and phenocryst-hosted melt inclusions.Quantitative simulation of crystallization of the parental magmain the Galmoenan magma chamber shows that the compositions ofthe cumulate units are best modelled by fractional crystallizationwith periodic magma replenishment. The model calculations reproducewell the observed mineral assemblages and the trace elementabundances in clinopyroxene. Based upon the estimated compositionof the parental magmas and their mantle source, we considerthat fluxing of a highly refractory mantle wedge (similar tothe source of boninites) by chlorine-rich aqueous fluids isprimarily responsible for both high degrees of partial meltingand the geochemical characteristics of the magmas, includingtheir enrichment in platinum-group elements. KEY WORDS: subduction; platinum-group elements; clinopyroxene; trace elements; fractional crystallization; Alaskan-type plutons  相似文献   

14.
Vesicular interstitial glass in four kaersutite-bearing spinel–wehrlitexenoliths from Foster Crater, Antarctica has reacted with hostolivine (Fo75–79) and clinopyroxene (Ca47 Mg45 Fe8) andcontains a microphenocryst assemblage of spinel, olivine, andclinopyroxene together with later rhonite and plagioclase. Electronmicroprobe analyses of the glasses have low SiO2 (46–49wt. per cent) and MgO (2.2–3.7) contents and high contentsof alkalis, TiO2 (3.4–4.8), Al2O3 (18.1–20.6) andP2O5 (1.1–1.3). Olivine microphenocryst cores in glassare magnesian (up to Fo88) and must have precipitated from moreprimitive liquids; rim compositions are Fe-rich (Fo75) and inequilibrium with glass. Continuous core to rim zonation in theolivine microphenocrysts indicate that glass compositions havefractionated due to crystallization of the enclosed mineralassemblage. Mass balance addition calculations, using the compositionsand proportions of the crystals in glass, produce melt compositionsappropriate to primary alkali basaltic magmas. Glasses showlight rare earth element (REE) enrichment relative to chondrites(Ce/YbN = 10.5) and, together with Ba, Rb, Cr, Hf, Ta, and Thare similar to many of the basanites from the Erebus VolcanicProvince. Textural relationships of the kaersutite are complex owing tothe instability of kaersutite in the presence of melt. However,in the association with glass we observe textural evidence suchas olivine and clinopyroxene microphenocrysts, identical tothe liquidus phases of the glasses, enclosed by kaersutite crystals.We believe that relationships such as this link the crystallizationof kaersutite to mafic melt which infiltrated and reacted withthe host wehrlite. Thus, the melt did not form in situ withinthe xenolith but originated elsewhere in the upper mantle.  相似文献   

15.
WIEBE  R.A. 《Journal of Petrology》1986,27(6):1253-1275
Nodules and xenocrysts dominated by high-A1 orthopyroxene occurin Proterozoic basaltic dikes that cut the Nain anorthositecomplex, Labrador. This pyroxene (En73–68, Al2O3 = 6.5–4.5)lacks exsolution and occurs both as anhedral xenocrysts up to10 cm in diameter and with euhedral plagioclase (An55) in ophiticnodules. Rarely, olivine (Fo70) occurs with orthopyroxene andAl-spinel with plagioclase. Scarce, more Fe-rich nodules containtwo pyroxenes (orthopyroxene + pigeonite and pigeonite+augite)and coarse intergrowths of ilmenite and Ti-rich magnetite. Pyroxenepairs yield temperatures of 1250? to 1170 ?C; coexisting oxidelamellae yield temperatures between 1145? and 1120 ?C. The highsubsolidus temperatures of the nodules contrasts with the lowtemperature of the host anorthosite at the time of dike emplacementand indicates a deep source for the nodules. Coexisting olivine(Fo70) and plagioclase (An54) suggest a maximum pressure ofabout 11 kb.The dominant orthopyroxene in these nodules is nearlyidentical in composition to the high-Al orthopyroxene megacrystswith exsolved plagioclase (HAOM) found in most Proterozoic anorthosites,and the ophitic nodules have textures similar to ophitic occurrencesof HAOM in anorthosite. Rafting of cotectic nodules from thelower crust can explain occurrences of HAOM in shallow levelanorthosites.The nodules and xenocrysts have compositions consistentwith crystallization from magmas that were parental to the anorthosites.They lend support to models which derive anorthosites by fractionalcrystallization of basaltic magma near the base of the crust.  相似文献   

16.
The well-preserved ?lower Proterozoic McIntosh intrusion consistsof 96 macro-layers with a total stratigraphic thickness of about6 km. The lowermost rocks in this possible cone-shaped intrusionare hidden, and the roof and the upper layers were removed byerosion. The layered sequence is dominated by 40 bimodal cyclicunits of troctolite and olivine gabbro. Minor gabbronorite layersoccur throughout the sequence, and are more abundant and morefractionated higher in the sequence. Six imperfect megacycicunits are developed in the upper 2700 m, each unit consistingof several troctolite-olivine gabbro cyclic units followed bya Fe-Ti oxide-bearing gabbronorite. The overall cumulus crystallizationorder in each megacyclic unit was plagioclase first, closelyfollowed by olivine, then augite, orthopyroxene, and magnetitesuccessively. Cryptic composition data for troctolites and olivine gabbrosshow a slight overall decrease of 10 mol per cent An and Fofrom the base to the top of the layered sequence (approximateranges An80–70 and Fo78–68). Several major fluctuationsoccur however, and are generally associated with the oxide gabbronorites,which are significantly more fractionated than the adjacentlayers (plagioclase An53–60, orthopyroxene Mg52–69Each fluctuation comprises a marked progressive discontinuity(rapid normal fractionation) followed by a gradual to rapidregressive discontinuity (or reversal) in the overlying troctolitesand olivine gabbros. Apparently, such marked progressive discontinuitieshave not been described in layered intrusions. A chilled margin and the overall composition of the intrusionsuggest an olivine tholeiite parent magma, inferred to havecrystallized at P 6 kb, relatively low PH2O and high fO2 (>NNO buffer). The troctolite-olivine gabbro cyclic units areinferred to have formed by fractional crystallization of periodicadditions of new magma. However, the oxide gabbronorites seemtoo fractionated relative to the underlying layers to have formedby conventional crystal fractionation mechanisms, and they couldhave resulted from a ‘liquid fractionation’ processin which fractionated residual magma, instead of rising, periodicallybecame denser and ponded on the temporary floor (a density crossover).Gradual, reversed cryptic trends in the cyclic units above theoxide gabbronorite layers may reflect mixing of this fractionatedmagma with successive magma additions.  相似文献   

17.
Two series of anhydrous experiments have been performed in anend-loaded piston cylinder apparatus on a primitive, mantle-derivedtholeiitic basalt at 1·0 GPa pressure and temperaturesin the range 1060–1330°C. The experimental data provideconstraints on phase equilibria, and solid and liquid compositionsalong the liquid line of descent of primary basaltic magmasdifferentiating in storage reservoirs located at the base ofthe continental crust. The first series are equilibrium crystallizationexperiments on a single basaltic bulk composition; the secondseries are fractionation experiments where near-perfect fractionalcrystallization was approached in a stepwise manner using 30°Ctemperature steps and starting compositions corresponding tothe liquid composition of the previous, higher-temperature glasscomposition. Liquids in the fractional crystallization experimentsevolve with progressive SiO2 increase from basalts to dacites,whereas the liquids in the equilibrium crystallization experimentsremain basaltic and display only a moderate SiO2 increase accompaniedby more pronounced Al2O3 enrichment. The principal phase equilibriacontrols responsible for these contrasting trends are suppressionof the peritectic olivine + liquid = opx reaction and earlierplagioclase saturation in the fractionation experiments comparedwith the equilibrium experiments. Both crystallization processeslead to the formation of large volumes of ultramafic cumulatesrelated to the suppression of plagioclase crystallization relativeto pyroxenes at high pressures. This is in contrast to low-pressurefractionation of tholeiitic liquids, where early plagioclasesaturation leads to the production of troctolites followed by(olivine-) gabbros at an early stage of differentiation. KEY WORDS: liquid line of descent; tholeiitic magmas; equilibrium crystallization; fractional crystallization  相似文献   

18.
In Central Dronning Maud Land, East Antarctica, rare metre-sizedlenses of spinel peridotite are enclosed in high-grade metamorphicrocks. The rocks experienced a medium-P granulite-facies metamorphismat 575 Ma and a low-P amphibolite-facies overprint at 530 Ma.The latter is probably related to extensive granitoid magmatismbetween 530 and 500 Ma, which produced large volumes (abouthalf of the outcrops today) of granitic to syenitic rocks aswell as abundant K-feldspar–quartz pegmatites. One ofthe spinel peridotite lenses in the Schirmacher Oasis of CentralDronning Maud Land is crosscut by several small (up to 10 cmwide) veins with a characteristic zoned sequence of mineralassemblages, which was formed by reaction of a hydrous, SiO2-saturatedfluid or pegmatitic melt with the peridotite. The zoned sequenceconsists of the following mineral assemblages (from the centreof the vein towards the outer margin): zone 0, plagioclase +quartz; zone 1, green biotite intergrown with zircon + clinoamphibole;zone 2, cummingtonite + dark brown biotite intergrown with rutile+ clinoamphibole; zone 3, cummingtonite + light brown biotite+ spinel; zone 4, olivine + orthopyroxene + spinel ±clinopyroxene (unaltered peridotite). This sequence was investigatedwith respect to its conditions of formation, modal mineralogy,mineral chemistry, fluid inclusions, and oxygen and hydrogenisotope compositions of selected minerals. Based on the stabilityof cummingtonite and on equilibrium calculations in the MgO–SiO2–H2Osystem and on quartz–biotite oxygen isotope thermometry,the reaction vein formed at 650°C, which is in accord withtypical pegmatite crystallization temperatures. The pegmatiteof zone 0 is interpreted to have formed in an open fissure whereas,on textural grounds, zone 3 replaces former peridotite. On thebasis of mass balance constraints, the boundary between zones1 and 2 is interpreted to approximately represent the formerboundary between peridotite and the open fissure before reaction.Oxygen isotope systematics show that the infiltrating fluidhad an isotopic composition of 9–10 SMOW. All mineralsof the reaction vein with the exception of the inherited spineland olivine in the adjacent peridotite are in equilibrium withsuch a fluid. Spinel in the peridotite is depleted in 18O comparedwith coexisting olivine, which suggests isotopic disequilibrium.Spinel in zone 3 has a distinctly different isotopic compositioncompared with that in the peridotite, apparently approachingbut not reaching equilibrium. The combination of mineral chemistryand mass balance constraints of the modal mineralogy constrainsthe volume change during metasomatism and the direction of elementaldiffusion. It is indicated that Mg, Cr and Ni always diffusedtowards the vein, whereas Si, Al, K, Na, H2O and possibly Fediffused into the peridotite. KEY WORDS: peridotite; metasomatism; pegmatite; diffusion; reaction  相似文献   

19.
Four assemblages from calcic pelitic schists from South Strafford,Vermont, have been studied in detail to determine the relationshipbetween reaction history and compositional zoning of minerals.The lowest-grade assemblage is garnet + biotite + chlorite +plagioclase + epidote + quartz + muscovite + graphite + fluid.Along a path of isobaric heating, the net reaction is Chl +Ms + Ep + Gr = Grt + Bt + Pl + fluid. Garnet grows with decreasingFe/(Fe + Mg) and XSpa, (from 0•2 to 0•05), XGra staysnearly constant between 0•20 and 0•25, and plagioclasegrows with XAn increasing from peristerite to 0•2–0•5. The subsequent evolution depends on whether chlorite or epidotereacts out first. If chlorite is removed from the assemblagefirst, the net reaction along an isobaric heating path becomesGrt + Ms + Ep + Qtz + Gr = Bt + Pl + fluid. XAn of plagioclaseincreases to 0•20–0•70, depending on the bulk-rockcomposition and changes in pressure and temperature. If epidoteis removed first, the assemblage becomes a simple pelite andthe net reaction becomes Chl + Pl + Ms + Qtz = Grt + Bt + H2O.Plagioclase is consumed to provide Ca for growing garnet, andXAn, Fe/(Fe + Mg) of garnet, XGra, and XSpa all decrease. Afterboth chlorite and epidote are removed, continued heating upto the metamorphic peak of {small tilde}600C produces littleprogress of the reaction Grt + Ms = Bt + Pl; and XAn increases. The four assemblages have been numerically modeled using theGibbs method starting with measured compositions. The modelssuccessfully predict the observed compositional zoning and trendsof mineral growth and consumption along the computed P–Tpaths. The models also predict the compositional mineral zoningthat would have resulted from other P–T paths. * Present address: Department of Geology, University of Alabama, Tuscaloosa, Alabama 35487  相似文献   

20.
Disequilibrium phenocryst assemblages in the Younger Andesitesand Dacites of Iztacc?huatl, a major Quaternary volcano in theTrans-Mexican Volcanic Belt, provide an excellent record ofepisodic replenishment, magma mixing, and crystallization processesin calc-alkaline magma chambers. Phenocryst compositions andtextures in ‘mixed’ lavas, produced by binary mixingof primitive olivine-phyric basalt and evolved hornblende dacitemagmas, are used to evaluate the mineralogical and thermal characteristicsof end-members and the physical and chemical interactions thatattend mixing. Basaltic end-members crystallized olivine (FO90–88) andminor chrome spinel during ascent into crustal magma chambers.Resident dacite magma contained phenocrysts of andesine (An45–35),hypersthene (En67–61), edenitic-pargasitic hornblende,biotite, quartz, .titanomagnetite, and ilmenite. On reachinghigh-level reservoirs, basaltic magmas were near their liquidiat temperatures of about 1250–1200?C according to theolivine-liquid geothermometer. Application of the Fe-Ti-oxidegeothermometer-oxygen barometer indicates that hornblende dacitemagma, comprising phenocrysts (<30 vol. per cent) and coexistingrhyolitic liquid, had an ambient temperature between 940 and820?C at fO2s approximately 0?3 log units above the nickel-nickeloxide buffer assemblage. Mixing induced undercooling of hybridliquids and rapid crystallization of skeletal olivine (Fo88–73),strongly-zoned clinopyroxene (endiopside-augite), calcic plagioclase(An65–60); and orthopyroxene (bronzite), whereas low-temperaturephenocrysts derived from hornblende dacite were resorbed ordecomposed by hybrid melts. Quartz reacted to form coronas ofacicular augite and hydroxylated silicates were heated to temperaturesabove their thermal stability limit ({small tilde}940?C foramphibole, according to clinopyroxene-orthopyroxene geothermometry,and {small tilde}880?C for biotite). Calculations of phenocrystresidence times in hybrid liquids based on reaction rates suggestthat the time lapse between magma chamber recharge and eruptionwas extremely short (hours to days). It is inferred that mixing of magmas of diverse compositionis driven by convective turbulence generated by large differencesin temperature between end-members. The mixing mechanism involves:(1)rapid homogenization of contrasting residual liquid compositionsby thermal erosion and diffusive transfer (liquid blending);(2) assimilation of phenocrysts derived from the low-temperatureend-member; and (3) dynamic fractional crystallization of rapidlyevolving hybrid liquids in a turbulent boundary layer separatingbasaltic and dacitic magmas. The mixed lavas of lztacc?huatlrepresent samples of this boundary layer quenched by eruption.  相似文献   

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