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1.
Basalt–basaltic andesite (<55 wt % SiO2) and dacite–rhyolite(66–74 wt % SiO2) are the predominant eruptive productsin the Sumisu caldera volcano, Izu–Bonin arc, Japan. Themost magnesian basalt (8·5% MgO), as well as some ofthe other basalts, has a low Zr content (20–25 ppm), andcannot yield basalts with higher Zr contents (29–40 ppm)through fractionation and/or assimilation. The high- and low-Zrbasalts have different phenocryst assemblages, olivine, plagioclaseand pyroxene phenocryst chemistries, REE (rare earth element)patterns, and fluid-mobile element/immobile element ratios.Estimated primary olivine compositions are more magnesian (>Fo91)in the low-Zr basalts compared with those in high-Zr basalts(<Fo89). The low-Zr basalts contain up to 11 vol. % augite,but many high-Zr basalts are free of augite, which appears onlyin their more differentiated products. The low-Zr basalts areconsidered to be hydrous magmas in which olivine crystallizesfirst followed by augite and plagioclase, whereas the high-Zrbasalts are dry. The low-Zr basalts have higher U/Th ratiosthan the high-Zr basalts. We suggest that both dry and wet primarybasalts existed in the Sumisu magmatic system, each having differenttrace element concentrations, mineral assemblages and mineralchemistry. The lower contents of Zr and light REE and magnesianprimary olivines in the wet basalts could have resulted froma higher degree of partial melting (20%) of a hydrous sourcemantle compared with 10% melting of a dry source mantle. TheSr, Nd and Pb isotope compositions of the wet and dry basaltsare similar and are limited in range. These lines of evidenceindicate that a mantle diapir model might be applicable to satisfythe configuration of such a mantle source region beneath a singlevolcanic system such as Sumisu. KEY WORDS: degree of melting; hot fingers; isotopes; mantle diapir; mantle wedge  相似文献   

2.
Komatiites from the 2 Ga Jeesiörova area in Finnish Laplandhave subchondritic Al2O3/TiO2 ratios like those in Al-depletedkomatiites from Barberton, South Africa. They are distinct inthat their Al abundances are higher than those of the Al-depletedrocks and similar to levels in Al-undepleted komatiites. Moderatelyincompatible elements such as Ti, Zr, Eu, and Gd are enriched.Neither majorite fractionation nor hydrous melting in a supra-subductionzone setting could have produced these komatiites. Their highconcentrations of moderately incompatible elements may haveresulted from contamination of their parental melt through interactionwith metasomatic assemblages in the lithospheric mantle or enrichmentof their mantle source in basaltic melt components. Re–Osisotope data for chromite from the Jeesiörova rocks yieldan average initial 187Os/188Os of 0·1131 ± 0·0006(2), Os(I) = 0·1 ± 0·5. These data, coupledwith an initial Nd of +4, indicate that melt parental to thekomatiites interacted minimally with ancient lithospheric mantle.If their mantle source was enriched in a basaltic component,the combined Os–Nd isotopic data limit the enrichmentprocess to within 200 Myr prior to the formation of the komatiites.Their Os–Nd isotopic composition is consistent with derivationfrom the contemporaneous convecting upper mantle. KEY WORDS: Finnish Lapland; Jeesiörova; komatiites; mantle geochemistry; petrogenesis; redox state; Re/Os isotopes; Ti enrichment  相似文献   

3.
The anhydrous phase relations of an uncontaminated (primitive),ferropicrite lava from the base of the Early Cretaceous Paraná–Etendekacontinental flood basalt province have been determined between1 atm and 7 GPa. The sample has high contents of MgO (14·9wt %), FeO* (14·9 wt %) and Ni (660 ppm). Olivine phenocrystshave maximum Fo contents of 85 and are in equilibrium with thebulk rock, assuming a of 0·32. A comparison of our results with previous experimental studiesof high-Mg rocks shows that the high FeO content of the ferropicritecauses an expansion of the liquidus crystallization field ofgarnet and clinopyroxene relative to olivine; orthopyroxenewas not observed in any of our experiments. The high FeO contentalso decreases solidus temperatures. Phase relations indicatethat the ferropicrite melt last equilibrated either at 2·2GPa with an olivine–clinopyroxene residue, or at 5 GPawith a garnet–clinopyroxene residue. The low bulk-rockAl2O3 content (9 wt %) and high [Gd/Yb]n ratio (3·1)are consistent with the presence of residual garnet in the ferropicritemelt source and favour high-pressure melting of a garnet pyroxenitesource. The garnet pyroxenite may represent subducted oceaniclithosphere entrained by the upwelling Tristan starting mantleplume head. During adiabatic decompression, intersection ofthe garnet pyroxenite solidus at 5 GPa would occur at a mantlepotential temperature of 1550°C and yield a ferropicriteprimary magma. Subsequent melting of the surrounding peridotiteat 4·5 GPa may be restricted by the thickness of theoverlying sub-continental lithosphere, such that dilution ofthe garnet pyroxenite melt component would be significantlyless than in intra-oceanic plate settings (where the lithosphereis thinner). This model may explain the limited occurrence offerropicrites at the base of continental flood basalt sequencesand their apparent absence in ocean-island basalt successions. KEY WORDS: continental flood basalt; ferropicrite; mantle heterogeneity; mantle melting; phase relations; pyroxenite  相似文献   

4.
The Wrangellia terrane of North America contains a large volumeof Middle to Late Triassic oceanic flood basalts which wereemplaced on top of a preexisting island arc. Nd-, Sr-, and Pb-isotopiccompositions reflect derivation from a plume source with Nd(T)+6 to + 7, 87Sr/86Sri0•7034, and 206Pb/204Pbi19•0.Major and trace element compositions suggest the Wrangelliaflood basalts (WFB) formed through relatively small degreesof partial melting at greater depths than estimated for otheroceanic plateaux such as Ontong Java. It appears that the WFBdid not form in a rifting environment, and that preexistingarc lithosphere limited the ascent and decompression meltingof the source plume. Rocks from the preexisting arc are stronglydepleted in high field strength elements (HFSEs) relative tolarge ion lithophile elements (LILEs), but the WFB are not.Assimilation of arc lithospheric mantle or crust was thereforegenerally minor. However, some contamination by arc componentsis evident, particularly in basalts erupted in the early stagesof volcanism. Minor isotopic shifts, to lower Nd(T) and 206Pb/204Pbiand higher 87Sr/86Sri, are accompanied by shifts in trace elementratios towards more arclike signatures, e.g. low Nb/Th and Nb/La.Arc contamination is greatest in the most evolved basalts, indicatingthat assimilation was coupled with fractional crystallization.A comparison of the WFB with other continental and oceanic floodbasalts reveals that continental flood basalts generally formthrough smaller degrees of melting than oceanic flood basaltsand that the contribution of material from the crust and litho-sphericmantle is significantly greater. KEY WORDS: oceanic flood basalts; Wrangellia terrane; petrogenesis; Sr-Nd-Pb isotopes *Corroponding author  相似文献   

5.
The Tertiary to Recent basalts of Victoria and Tasmania havemineralogical and major element characteristics of magmas encompassingthe range from quartz tholeiites to olivine melilitites. Abundancesof trace elements such as incompatible elements, including therare earth elements (REE), and the compatible elements Ni, Coand Sc, vary systematically through this compositional spectrum.On the basis of included mantle xenoliths, appropriate 100 Mg/Mg+ Fe+2 (68–72) and high Ni contents many of these basaltsrepresent primary magmas (i.e., unmodified partial melts ofmantle peridotite). For fractionated basalts we have derivedmodel primary magma compositions by estimating the compositionalchanges caused by fractional crystallization of olivine andpyroxene at low or moderate pressure. A pyrolite model mantlecomposition has been used to establish and evaluate partialmelting models for these primary magmas. By definition and experimentaltesting the specific pyrolite composition yields parental olivinetholeiite magma similar to that of KilaeauIki, Hawaii (1959–60)and residual harzburgite by 33 per cent melting. It is shownthat a source pyrolite composition differing only in having0.3–0.4 per cent TiO2 rather than 0.7 per cent TiO2, isable to yield the spectrum of primary basalts for the Victorian-Tasmanianprovince by 4 per cent to 25 per cent partial melting. The mineralogiesof residual peridotites are consistent with known liquidus phaserelationships of the primary magmas at high pressures and thechemical compositions of residual peridotite are similar tonatural depleted or refractory lherzolites and harzburgites.For low degrees of melting the nature of the liquid and of theresidual peridotite are sensitively dependent on the contentof H2O, CO2 and the CO2/H2O in the source pyrolite. The melting models have been tested for their ability to accountfor the minor and trace element, particularly the distinctivelyfractionated REE, contents of the primary magmas. A single sourcepyrolite composition can yield the observed minor and traceelement abundances (within at most a factor of 2 and commonlymuch closer) for olivine melilitite (4–6 per cent melt),olivine nephelinite, basanite (5–7 per cent melt), alkaliolivine basalt (11–15 per cent melt), olivine basalt andolivine tholeiite (20–25 per cent melt) provided thatthe source pyrolite was already enriched in strongly incompatibleelements (Ba, Sr, Th, U, LREE) at 6–9 x chondritic abundancesand less enriched (2.5–3 x chondrites) in moderately incompatible(Ti, Zr, Hf, Y, HREE) prior to the partial melting event. Thesources regions for S.E. Australian basalts are similar to thosefor oceanic island basalts (Hawaii, Comores, Iceland, Azores)or for continental and rift-valley basaltic provinces and verydifferent in trace element abundances from the model sourceregions for most mid-ocean ridge basalts. We infer that thismantle heterogeneity has resulted from migration within theupper mantle (LVZ or below the LVZ) of a melt or fluid (H2O,CO2-enriched) with incompatible element concentrations similarto those of olivine melilitite, kimberlite or carbonatite. Asa result of this migration, some mantle regions are enrichedin incompatible elements and other areas are depleted. Although it is possible, within the general framework of a lherzolitesource composition, to derive the basanites, olivine nephelinitesand olivine melilitites from a source rock with chondritic relativeREE abundances at 2–5 x chondritic levels, these modelsrequire extremely small degrees of melting (0.4 per cent forolivine melilitite to 1 per cent for basanite). Furthermore,it is not possible to derive the olivine tholeiite magmas fromsource regions with chondritic relative REE abundances withoutconflicting with major element and experimental petrology argumentsrequiring high degrees (15 per cent) of melting and the absenceof residual garnet. If these arguments are disregarded, andpartial melting models are constrained to source regions withchondritic relative REE abundances, then magmas from olivinemelilitites to olivine tholeiites can be modelled if degreesof melting are sufficiently small, e.g., 7 per cent meltingfor olivine tholeiite. However, the source regions must be heterogenousfrom 1 to 5 x chondritic in absolute REE abundances and heterogerieousin other trace elements as well. This model is rejected in favorof the model requiring variation in degree of melting from 4per cent to 25 per cent and mantle source regions ranging fromLREE-enriched to LREE-depleted relative to chondritic REE abundances.  相似文献   

6.
A suite of dolerite dykes from the Ahlmannryggen region of westernDronning Maud Land (Antarctica) forms part of the much moreextensive Karoo igneous province of southern Africa. The dykecompositions include both low- and high-Ti magma types, includingpicrites and ferropicrites. New 40Ar/39Ar age determinationsfor the Ahlmannryggen intrusions indicate two ages of emplacementat 178 and 190 Ma. Four geochemical groups of dykes have beenidentified in the Ahlmannryggen region based on analyses of60 dykes. The groups are defined on the basis of whole-rockTiO2 and Zr contents, and reinforced by rare earth element (REE),87Sr/86Sr and 143Nd/144Nd isotope data. Group 1 were intrudedat 190 Ma and have low TiO2 and Zr contents and a significantArchaean crustal component, but also evidence of hydrothermalalteration. Group 2 dykes were intruded at 178 Ma; they havelow to moderate TiO2 and Zr contents and are interpreted tobe the result of mixing of melts derived from an isotopicallydepleted source with small melt fractions of an enriched lithosphericmantle source. Group 3 dyke were intruded at 190 Ma and formthe most distinct magma group; these are largely picritic withsuperficially mid-ocean ridge basalt (MORB)-like chemistry (flatREE patterns, 87Sr/86Sri 0·7035, Ndi 9). However, theyhave very high TiO2 (4 wt %) and Zr (500 ppm) contents, whichis not consistent with melting of MORB-source mantle. The Group3 magmas are inferred to be derived by partial melting of astrongly depleted mantle source in the garnet stability field.This group includes several high Mg–Fe dykes (ferropicrites),which are interpreted as high-temperature melts. Some Group3 dykes also show evidence of contamination by continental crust.Group 4 dykes are low-K picrites intruded at 178 Ma; they havevery high TiO2–Zr contents and are the most enriched magmagroup of the Karoo–Antarctic province, with ocean-islandbasalt (OIB)-like chemistry. Dykes of Group 1 and Group 3 aresub-parallel (ENE–WSW) and both groups were emplaced at190 Ma in response to the same regional stress field, whichhad changed by 178 Ma, when Group 2 and Group 4 dykes were intrudedalong a dominantly NNE–SSW strike. KEY WORDS: flood basalt; depleted mantle; enriched mantle; Ahlmannryggen; Karoo dyke  相似文献   

7.
Early Cretaceous tholeiitic picrite-to-rhyolite dykes aroundSpitzkoppe, western Namibia, are part of the extensive HentiesBay–Outjo swarm, penecontemporaneous with 132 Ma Etendekalavas 100 km to the NW. Although only intermediate to rhyoliticdykes contain clinopyroxene phenocrysts, the behaviour of Ca,Al and Sc in the dyke suite shows that liquidus clinopyroxene—togetherwith olivine—was a fractionating phase when MgO fell to9 wt %. Both a plot of CIPW normative di–hy–ol–ne–Qand modelling using (p)MELTS show that a mid-crustal pressureof 0·6 GPa is consistent with this early clinopyroxenesaturation. Sr, Nd, Hf and Pb isotope variations all show trendsconsistent with AFC contamination (assimilation linked to fractionalcrystallization), involving Pan-African Damara belt continentalcrust. The geochemical variation, including isenthalpic AFCmodelling using (p)MELTS, suggests that the picrites (olivine-richcumulate suspensions) were interacting with granulite-faciesmetamorphic lower crust, the intermediate compositions withamphibolite-facies middle crust, and the rhyolitic dykes (anda few of the basalts) with the Pan-African granites of the uppercrust. The calculated densities of the magmas fall systematicallyfrom picrite to rhyolite and suggest a magmatic system resemblinga stack of sills throughout the crust beneath Spitzkoppe, withthe storage and fractionation depth of each magma fraction controlledby its density. Elemental and isotopic features of the 20 wt% MgO picrites (including Os isotopes) suggest that their parentalmelts probably originated by fusion of mid-ocean ridge basalt(MORB) source convecting mantle, followed by limited reactionwith sub-continental lithospheric mantle metasomatized justprior to the formation of the parental magmas. Many of the distinctivefeatures of large-volume picritic–basaltic magmas maynot be derived from their ultimate mantle sources, but may insteadbe the results of complex polybaric fractional crystallizationand multi-component crustal contamination. KEY WORDS: flood basalts; Spitzkoppe; picrite; trace elements; hafnium isotopes; Etendeka  相似文献   

8.
Different lithologies (impure marble, eclogite and graniticorthogneiss) sampled from a restricted area of the coesite-bearingBrossasco–Isasca Unit (Dora Maira Massif) have been investigatedto examine the behaviour of 40Ar–39Ar and Rb–Srsystems in phengites developed under ultrahigh-pressure (UHP)metamorphism. Mineralogical and petrological data indicate thatzoned phengites record distinct segments of the PT path:prograde, peak to early retrograde in the marble, peak to earlyretrograde in the eclogite, and late retrograde in the orthogneiss.Besides major element zoning, ion microprobe analysis of phengitein the marble also reveals a pronounced zoning of trace elements(including Rb and Sr). 40Ar–39Ar apparent ages (35–62Ma, marble; 89–170 Ma, eclogite; 35–52 Ma, orthogneiss),determined through Ar laserprobe data on phengites (step-heatingand in situ techniques), show wide intra-sample and inter-samplevariations closely linked to within-sample microchemical variations:apparent ages decrease with decreasing celadonite contents.These data confirm previous reports on excess Ar and, more significantly,highlight that phengite acted as a closed system in the differentlithologies and that chemical exchange, not volume diffusion,was the main factor controlling the rate of Ar transport. Conversely,a Rb–Sr internal isochron from the same eclogite yieldsan age of 36 Ma, overlapping with the time of the UHP metamorphicpeak determined through U–Pb data and thereby corroboratingthe previous conclusion that UHP metamorphism and early retrogressionoccurred in close succession. Different phengite fractions ofthe marble yield calcite–phengite isochron ages of 36to 60 Ma. Although this time interval matches Ar ages from thesame sample, Rb–Sr data from phengite are not entirelyconsistent with the whole dataset. According to trace elementvariations in phengite, only Rb–Sr data from two wet-groundphengite separates, yielding ages of 36 and 41 Ma, are internallyconsistent. The oldest age obtained from a millimetre-sizedgrain fraction enriched in prograde–peak phengites mayrepresent a minimum age estimate for the prograde phengite relics.Results highlight the potential of the in situ 40Ar–39Arlaser technique in resolving discrete PT stages experiencedby eclogite-facies rocks (provided that excess Ar is demonstrablya negligible factor), and confirm the potential of Rb–Srinternal mineral isochrons in providing precise crystallizationages for eclogite-facies mineral assemblages. KEY WORDS: 40Ar–39Ar dating; Rb–Sr dating; phengite; SIMS; UHP metamorphism  相似文献   

9.
Potassic volcanism has been widespread and semi-continuous onthe Tibetan plateau since 13 Ma, post-dating the orogenic thickeningof the India-Asia collision. Volcanism may have commenced slightlyearlier (16–20 Ma) in the southern portion of the plateauand then ceased around 10 Ma. The dominant lavas are pyroxen-and plagioclase-phyric shoshonites with subordinate occurrencesof dacites and rhyolites. Their mineralogy reflects crystallizationfrom high-temperature (1100C) magmas which had elevated oxygenand water fugacities. Geochemically, they are characterizedby relatively low TiO2, Al2O3 and Fe2O3, and high Na2O, coupledwith variable abundances of compatible trace elements and veryhigh contents of incompatible trace elements. Normalized incompatibleelement patterns have marked negative Nb, Ta and Ti anomalieswhereas K2O appears to be buffered at 4% over a wide range ofSiO2. Isotope data show a relatively broad and enriched rangeof 87Sr/86 Sr (0.7076–0.7106) at more restricted ENd (–5.2to –8.1). Pb isotopes are characterized by a range of207Pb/204 Pb (15.51–15.72) and 208 Pb/204Pb (38.67–39.30) at very uniform 206Pb/204 Pb (18.39–18.83), leadingto vertical arrays. Volcanics from the southern parts of theplateau have more primitive isotopic compositions: 87Sr/86 Sr0.7048–0.7080, Nd 1.4 to –3.3, 206Pb/204 Pb 18.48–18.67,207Pb/204 Pb 15.59–15.68 and 208Pb/204 Pb 38. 73–38.98. In general, the geochemical and isotopic data most closely approximatepartial melting arrays, although fractionation processes haveclearly operated. The isotopic ratios and the enrichment ofincompatible elements and LREE/HREE cannot be derived from adepleted mantle source via a single-stage melting process. Instead,a metasomatized, garnet peridotite source containing 6% phlogopiteis required and this is inferred to lie within the lithosphericmantle. The enrichment in incompatible elements in this sourcemust have been sufficiently ancient to generate the observedisotopic ratios, and Nd depleted mantle model ages suggest thiswas Proterozoic in age (1.2 Ga), whereas Pb model ages recordan Archaean event, suggesting the source had a multi-stage enrichmenthistory. The negative Ta, Nb and Ti anomalies and low Rb/Basuggest that metasomatism may have occurred during an ancientsubduction episode. The high 208Pb/204Pb, 207Pb/204 Pb and lowNb/U, Ce/Pb of the Tibetan shoshonites are distinct from oceanisland basalts. Thus, if convectively removed lithospheric mantleprovides a source for ocean island basalts, it must differ significantlyfrom the source of the Tibetan shoshonites. A lithospheric mantle source for the volcanism places importantconstraints on geodynamic models for the evolution of the Tibetanplateau and the India-Asia collision. For likely thermal structuresbeneath the plateau, the temperatures required to trigger meltingwithin the lithospheric mantle can only be plausibly obtainedif the lower parts of the lithospheric mantle were removed byconvective thinning. This is consistent with recent models whichinvoke the same process to explain the current elevation andextensional deformation of the plateau. The age data suggestthis occurred at 13 Ma and the duration of volcanism may beexplained by continued conductive heating since that time. Poorlysampled but slightly older volcanics from the southern portionsof the plateau may indicate that convective thinning began inthe south and migrated northwards. Rapid uplift of the plateaumay have resulted in increased rates of chemical weathering,which led to global cooling, as indicated by oxygen isotopedata from Atlantic sediments. KEY WORDS: Climate; lithospheric mantle; OIB; Tibet; volcanism *Corresponding author.  相似文献   

10.
High-pressure (HP) metamorphic blocks enclosed in a mafic toultramafic matrix from a mélange on the island of Syrosare rimmed by tourmaline-bearing reaction zones (blackwalls).The B isotopic composition of dravitic tourmaline within theseblackwalls was investigated in situ by secondary ion mass spectrometry.Boron in these tourmalines is unusually heavy, with 11B valuesexceeding +18 in all investigated samples and reaching an extremevalue of +28·4 in one sample. Blackwalls formed duringexhumation of the HP mélange at a depth of 20–25km at temperatures of 400–430°C, by influx of externalhydrous fluids. The compositions of the fluids are estimatedto be in the range of 100–300 µg/g B with 11B valuesof +18 to +28. The high 11B values cannot be explained by tourmalineformation from unmodified slab-derived fluids. However, suchfluids could interact with the material in the exhumation channelon their way from the dehydrating slab to the site of tourmalineformation in the blackwalls. This could produce exceptionallyhigh 11B values in the fluids, a case that is modelled in thisstudy. The model demonstrates that subduction fluids may beeffectively modified in both trace element and isotopic compositionduring their migration through the material overlying the subductingslab. Blackwall tourmaline from Syros has a large grain size(several centimetres), high abundance, and an exceptionallyhigh 11B value. The formation of tourmaline at the contact betweenmafic or felsic HP blocks and their ultramafic matrix involvedfluids released during dehydration reactions in the subductingslab. It forms a heavy-boron reservoir in hybrid rocks overlyingthe subducting slab, and may, thus, have a significant impacton the geochemical cycle of B and its isotopes in subductionzones. KEY WORDS: boron isotopes; tourmaline; subduction zone; fluid, high pressure  相似文献   

11.
Hafnium isotope and incompatible trace element data are presentedfor a suite of mid-ocean ridge basalts (MORB) from 13 to 47°Eon the Southwest Indian Ridge (SWIR), one of the slowest spreadingand most isotopically heterogeneous mid-ocean ridges. Variationsin Nd–Hf isotope compositions and Lu/Hf ratios clearlydistinguish an Atlantic–Pacific-type MORB source, presentwest of 26°E, characterized by relatively low Hf valuesfor a given Nd relative to the regression line through all Nd–Hfisotope data for oceanic basalts (termed the ‘Nd–Hfmantle array line’; the deviation from this line is termedHf) and low Lu/Hf ratios, from an Indian Ocean-type MORB signature,present east of 32°E, characterized by relatively high Hfvalues and Lu/Hf ratios. Additionally, two localized, isotopicallyanomalous areas, at 13–15°E and 39–41°E,are characterized by distinctly low negative and high positiveHf values, respectively. The low Hf MORB from 13 to 15°Eappear to reflect contamination by HIMU-type mantle from thenearby Bouvet mantle plume, whereas the trace element and isotopiccompositions of MORB from 39 to 41°E are most consistentwith contamination by metasomatized Archean continental lithosphericmantle. Relatively small source-melt fractionation of Lu/Hfrelative to Sm/Nd, compared with MORB from faster-spreadingridges, argues against a significant role for garnet pyroxenitein the generation of most central SWIR MORB. Correlations betweenHf and Sr and Pb isotopic and trace element ratios clearly delineatea high-Hf ‘Indian Ocean mantle component’ that canexplain the isotope composition of most Indian Ocean MORB asmixtures between this component and a heterogeneous Atlantic–Pacific-typeMORB source. The Hf, Nd and Sr isotope compositions of IndianOcean MORB appear to be most consistent with the hypothesisthat this component represents fragments of subduction-modifiedlithospheric mantle beneath Proterozoic orogenic belts thatfoundered into the nascent Indian Ocean upper mantle duringthe Mesozoic breakup of Gondwana. KEY WORDS: mid-ocean ridge basalt; isotopes; incompatible elements; Indian Ocean  相似文献   

12.
We have determined the near-solidus melt compositions for peridotiteMM-3, a suitable composition for the production of mid-oceanridge basalt (MORB) by decompression partial melting, at 1 and1·5 GPa. At 1 GPa the MM-3 composition has a subsolidusplagioclase-bearing spinel lherzolite assemblage, and a solidusat 1270°C. At only 5°C above the solidus, 4% meltis present as a result of almost complete melting of plagioclase.This melting behaviour in plagioclase lherzolite is predictedfrom simple systems and previous experimental work. The persistenceof plagioclase to > 0·8 GPa is strongly dependenton bulk-rock CaO/Na2O and normative plagioclase content in theperidotite. At 1·5 GPa the MM-3 composition has a subsolidusspinel lherzolite assemblage, and a solidus at 1350°C.We have determined a near-solidus melt composition at 2% meltingwithin 10°C of the solidus. Near-solidus melts at both 1and 1·5 GPa are nepheline normative, and have low normativediopside contents; also they have the highest TiO2, Al2O3 andNa2O, and the lowest FeO and Cr2O3 contents compared with higherdegree partial melts. Comparison of these near-solidus meltswith primitive MORB glasses, which lie in the olivine-only fieldof crystallization at low pressure, indicate that petrogeneticmodels involving aggregation of near-fractional melts formedduring melting at pressures of 1·5 GPa or less are unlikelyto be correct. In this study we use an experimental approachthat utilizes sintered oxide mix starting materials and peridotitereaction experiments. We also examine some recent studies usingan alternative approach of melt migration into, and entrapmentwithin ‘melt traps’ (olivine, diamond, vitreouscarbon) and discuss optimal procedures for this method. KEY WORDS: experimental petrology; mantle melting; near-solidus; fertile peridotite; MORB  相似文献   

13.
Zoisite-bearing high-pressure pegmatites from the MünchbergMassif, Germany, provide an excellent example of the characteristicsof the onset of metabasite melting at eclogite-facies conditions.The pegmatites were derived by partial melting of a mid-oceanridge basalt (MORB)-like eclogite at T 680°C/2·3GPa to 750°C/3·1 GPa, which produced small amountsof tonalitic to trondhjemitic melt. The melt concentrated locallyin isolated, small melt pockets and crystallized primary zoisiteas liquidus phase at P 2·3 GPa/680°C to 2·1GPa/750°C. Compositional zoning of pegmatite zoisite recordsan ensuing multi-stage uplift history with successive, discretecrystallization events at 1·4 ± 0·2 GPa/650–700°Cand 1·0 ± 0·1 GPa/620–650°C.Resorption textures indicate reheating and thermal perturbationof the whole system prior to each successive crystallizationevent. Final solidification of zoisite-pegmatites occurred at0·9 ± 0·1 GPa/620–650°C. Thedata suggest that isolated melt + zoisite crystal mush pocketsformed an integral part of the eclogite throughout uplift frommelt formation at T 680°C/2·3 GPa to 750°C/3·1GPa to final solidification at 0·9 GPa/620–630°C;that is, over a depth range of 45–60 km. The entire pegmatite-formingprocess was probably fluid conserving: fluid present duringmelt formation was trapped by fully or nearly water-saturatedsiliceous melts, whereas fluid liberated during pegmatite crystallizationinteracted with dehydrated eclogite-facies assemblages to formamphibolite-facies hydrous minerals. A set of empirical Dmelt/eclogitevalues based on mean zoisite-pegmatite and eclogite compositionwere used to model the onset of partial high-pressure meltingof metabasites. KEY WORDS: adakite; high-pressure melting; pegmatite; trondhjemite; zoisite  相似文献   

14.
The digital image of airborne radiometric data across SouthAfrica reveals that the largest anomaly, 100 nGy/h, is causedby the granulite-facies rocks of the Namaquan metamorphic complex,whereas most of the country is <60 nGy/h. This observationis consistent with geochemical data that show that the 1900± 100 Ma greenschist-facies Richtersveld Terrane nearNamibia (max. U = 3·4 ppm; Th = 20·1 ppm) andthe adjacent, 1100 ± 100 Ma, amphibolite-facies Aggeneys/SteinkopfTerranes (max. U 10 ppm; Th 52 ppm) are the least enrichedin U, Th and K. In contrast, the lower-T granulite-facies OkiepTerrane near Springbok hosts more enriched granites (max. U 17 ppm; Th 66 ppm) and noritic intrusions (max. U = 14 ppm;Th = 83 ppm). The most enriched rocks are found in the 1030Ma higher-T granulite-facies core of the Namaquan belt and includequartzo-feldspathic gneisses (max. U = 46 ppm; Th = 90 ppm)and charnockites (max. U = 52 ppm; Th = 400 ppm). Our findingscontradict the notion that granulite-facies terrains are characteristicallydepleted in U and Th. In this study we modeled the heat productionin the core of the Namaquan complex, where the granulites havehad a very unusual metamorphic history, and show that ultra-high-T(1000°C, P 10 kbar) metamorphic conditions could have beenachieved by radiogenic heating without invoking external heatsources. However, monazite-rich veins of charnockite and patchesof granulites mark the passage of CO2-dominated melts and fluidsderived from fractionated noritic intrusions. KEY WORDS: charnockite; granulite; Namaqualand; thorium; uranium; radioactive heating; metamorphism  相似文献   

15.
The southeastern margin of the anorthositic Kunene IntrusiveComplex, NW Namibia, has been subsequently invaded by Mesoproterozoicsyenite, nepheline syenite and ferrocarbonatite dykes alongNE- and SE-trending faults. The first generation of carbonatiteintrusions frequently contains fenitized anorthositic wall-rockfragments set in a ferrocarbonatite matrix; later, subordinateveins of massive ferrocarbonatite are almost xenolith-free andcut through the main carbonatite dykes. A mantle source forboth carbonatite generations is constrained by their respectiveoxygen and carbon isotope compositions of ankerite (18OSMOW8·91–9·73; 13CPDB –6·98 to–6·76). Na-rich fluids, released from the meltparental to the ferrocarbonatites, caused the fenitization ofboth the incorporated anorthosite xenoliths and the borderinganorthosite, syenite and nepheline syenite. This process ismainly characterized by the progressive transformation of Ca-richplagioclase, K-feldspar and nepheline into albite and/or sodalite.The changing mineral modes indicate that the fenitizing fluidswere sodium-rich and strongly Si-deficient solutions, whichalso contained significant amounts of Sr, Ba, Nb and the lightrare earth elements. On the basis of mineral equilibria studies,it is possible to reconstruct the temperature conditions forcarbonatite emplacement (c. 830 ± 200°C) and recrystallization(c. 480 ± 130°C), and for the metasomatic formationof sodalite (c. 700 ± 70°C). KEY WORDS: anorthosite; fenitization; ferrocarbonatite; sodalite; stable isotopes  相似文献   

16.
The subaerial part of the Stromboli stratovolcano was builtup in the last 100 kyr through six periods of activity; theerupted magmas record the largest compositional variation ofall the Aeolian arc volcanoes (calc-alkaline, shoshonitic, andpotassic alkaline magma series). The trace element characteristicsof the less evolved magmas of each period of activity are coherentlycorrelated with their radiogenic isotope (Sr, Nd, Pb) composition,and are typical of volcanic arc rocks. In terms of U-seriesisotopes, samples from the different magma series have both238U and 230Th excesses, and this distinctive feature providesadditional constraints on source enrichment processes withinthe mantle wedge and on the mechanism of partial melting. Overallthe complete set of data demonstrates that the genesis of thedifferent magma series at Stromboli can be accommodated in amantle source that experienced two distinct enrichment processesby different parts of the subducting oceanic crust of the Ionianslab. The first was caused by supercritical liquids originatingfrom the basaltic and sedimentary parts of the subducting slabat >5 GPa and 900°C. The second was induced by aqueousfluids, again originating from the basaltic and sedimentaryparts of the slab, released from a shallower part of the subductedIonian slab (< 5 GPa and 800°C). U–Th disequilibriaconstrain the timing of the first metasomatic event (Stage I:supercritical liquids) at >435 ka, whereas the second event(Stage II: aqueous fluids) occurred at 100 ka. The high-angledip of the Ionian slab (70°) caused the superimpositionof the metasomatizing agents of the two enrichment processesin the same volume of the mantle wedge, explaining the occurrenceof such different magma series in a single volcanic edifice.The U–Th disequilibria provide evidence for dynamic meltingof the metasomatized mantle wedge combined with an ageing effectresulting from the restoration of secular equilibrium afterthe perturbation caused by the U-rich aqueous fluids of StageII. The trace element and radiogenic isotope (U, Th, Sr, Nd,Pb) signature of the mantle source of the magmas at Stromboliis thus dependent upon the amount of supercritical liquids andaqueous fluids released by the two components of the subductedslab, whereas the distinctive 238U and 230Th excesses of themagmas result from a combination of mantle ageing and time-dependentdynamic melting. The geochemical and radiogenic isotope signatureof the mantle source beneath Stromboli places important constraintson the isotopic polarity from Southern Latium to the Aeolianarc attributed to the effect of a HIMU mantle component followingeither lateral inflow of foreland mantle material or upwellingof a mantle plume in the centre of the Tyrrhenian basin. Ourgeochemical model demonstrates that the high 206Pb/204Pb ofthe putative ‘HIMU’ mantle component could be equallyformed during metasomatism of the pre-existing mantle wedgeby either the supercritical liquid (Stage I) or aqueous fluid(Stage II) released by the subducted altered basalt of the Ionianplate. KEY WORDS: radiogenic isotopes; U–Th disequilibria; mantle metasomatism; supercritical liquid; aqueous fluid; Stromboli  相似文献   

17.
The paper presents U–Pb ages for zircon, titanite, andmonazite, and Hf isotopic data for zircon, from the rocks oftwo magmatic suites occurring mostly in the Archean Uchi Subprovinceand partly in the neighbouring Berens River and English Riversubprovinces of the northwestern Superior Province, Ontario.These data, together with observations on the morphologies and,where evident, the inheritance of the zircon crystals, constrainthe nature of the sources of the magmas and provide a recordof various crustal processes in their evolution. The older of the two magmatic suites formed at 2744–2740Ma along segments of a common arc system. The suite consistsof (1) several trondhjemitic to granodioritic plutons, withHf values of 6•1, intruded into older crust and possiblyformed from magma produced by partial melting of subducted,juvenile oceanic crust; (2) an assemblage of dacitic pyroclasticvolcanic rocks, with Hf values of 3•2–4•0, associatedwith tholeiitic basalts and probably derived from magma meltedfrom arc mantle; and (3) a bimodal assemblage of tholeiiticbasalts, rhyolites, and porphyries, also with Hf values of 6•1,associated with a volcanogenic massive sulphide deposit andapparently formed by differentiation of mantle-derived basalticmelts at shallow levels in an extensional back-arc setting. The second magmatic suite, formed between 2702 and 2693 Ma,comprises late orogenic plutons and batholiths of dioritic todominantly granodioritic composition. The characteristics ofthese intrusions are consistent with a process combining meltingof a metasomatized mantle source and subsequent fractional crystallizationof the derived magmas at shallow depths. However, most of thestudied occurrences show evidence of crustal contamination throughvarious combinations of assimilation of lower-crustal material,assimilation of underthrust sedimentary rocks, and contaminationby wall rock materials during the latest stages in the emplacementof the plutons. The involvement of crustal material is indicatedby the presence of zircon xenocrysts and by Hf values rangingfrom 1•4 to 4•4. Only one intrusion, with an Hf valueof 5•0 and no xenocrystic zircon, appears to have escapedwidespread contamination, perhaps because the ascent of itsmagma was facilitated by a crustal-scale fracture system.  相似文献   

18.
We present trace element and Sr–Nd–Hf–Pb isotopecompositions for clinopyroxenes from anhydrous spinel peridotiteand garnet ± spinel pyroxenite xenoliths of Pan-Africanlithospheric mantle from Jordan, including the first high-precisiondouble-spike Pb isotope measurements of mantle clinopyroxene.Clinopyroxenes from the peridotites are variably Th–U–LILE–LREEenriched and display prominent negative Nb, Zr and Ti anomalies.MREE–HREE abundances can generally be modelled as partialmelting residues of spinel lherzolite with primitive-mantle-likecomposition after extraction of 5–10% melt, whereas theenrichments in Th–U–LILE–LREE require a Pan-Africanor later metasomatic event. The large range of Nd, Sr, Pb andHf isotope ratios in both peridotites and pyroxenites (e.g.Nd 1·4–17·5; 206Pb/204Pb 17·2–20·4;Hf 0·6–164·6) encompasses compositionsmore radiogenic than mid-ocean ridge basalt (MORB), and Pb isotopescover almost the entire range of oceanic basalt values. Hf valuesare some of the highest ever recorded in mantle samples andare decoupled from Nd in the same samples. Marked correlationsbetween Sr–Nd–Pb isotopes, LILE–LREE enrichmentsand HFSE depletion suggest that the metasomatizing agent wasa carbonatitic-rich melt and isotopic data suggest that metasomatismmay have been related to Pan-African subduction. The metasomaticmelt permeated depleted upper mantle (<16 kbar) during Pan-Africansubduction at 600–900 Ma, and the variably metasomatizedmaterial was then incorporated into the Arabian lithosphericmantle. There is no evidence for recent metasomatism (<30Ma) related to the Afar plume like that postulated to have affectedsouthern Arabian lithospheric mantle. Hf isotopes in the mantleclinopyroxenes are unaffected by metasomatism, and even somestrongly overprinted lithologies record ancient (>1·2Ga) pre-metasomatic Lu–Hf signatures of the depleted uppermantle that was the protolith of the Arabian lithospheric mantle.The ‘resistance’ of the Lu–Hf isotopic systemto later metasomatic events resulted in the development of extremelyheterogeneous Hf isotopic signatures over time that are decoupledfrom other isotopic systems. No mantle sample in this studyexactly matches the chemical and isotopic signature of the sourceof Jordanian intraplate basalts. However, the xenolith compositionsare broadly similar to those of the source of Arabian intraplatebasalts, suggesting that the numerous Cenozoic intraplate volcanicfields throughout Arabia may be the product of melting uppermantle wedge material fertilized during Pan-African subductionand incorporated into the Arabian lithospheric mantle. We proposea model whereby the proto-Arabian lithospheric mantle underwenta major melting event in early Proterozoic–late Archeantimes (at the earliest at 1·2 Ga). Island-arc volcanismand major crust formation occurred during the Pan-African orogeny,which liberated fluids and possibly small-degree melts thatmigrated through the mantle creating zones of enrichment forcertain elements depending upon their compatibility. Immobileelements, such as Nb, were concentrated near the base of themantle wedge providing the source of the Nb-rich Jordanian volcanicrocks. More mobile elements, such as LILE and LREE, were transportedup through the mantle and fertilized the shallow mantle sourceof the Jordanian xenoliths. Following subduction, the mantlewedge became fossilized and preserved distinct enriched anddepleted zones. Lithospheric rifting in the Miocene triggeredpartial melting of spinel-facies mantle in the lower lithosphere,which mixed with deeper asthenospheric garnet-facies melts asrifting evolved. These melts entrained segments of variablycarbonatite-metasomatized shallow lithospheric mantle en routeto the surface. KEY WORDS: Arabian lithospheric mantle; Jordan; mantle xenoliths; Sr–Nd–Hf–Pb isotopes  相似文献   

19.
The voluminous, bimodal, Silurian Topsails igneous suite consistsmainly of ‘A-type’ peralkaline to slightly peraluminous,hypersohnis to subsolvus granites with subordinate syenite,onzonite and diabase, plus consanguineous basalts and highsilicarhyolites. Nd(T) values from the suite range from –1.5to +5.4; most granitoid components exhibit positive Nd(T) values(+1.1 to +3.9). Granitoid initial 87Sr/86Sr and most 18 O valuesare in the range expected for rocks derived from mantle-likeprotoliths (0.701–0.706 and +6 to +80/). Restricted 207Pb/204Pbvariation is accompanied by significant dispersion of 206Pb/204Pband 208Pb/204Pb. Superficially, petrogenesis by either direct(via fractionation from basalt) or indirect (via melting ofjuvenile crust) derivation from mantle sources appears plausible.Remelting of the granulitic protolith of Ordovician are-typegranitoids can be ruled out, because these rocks exhibit negativeNd(T) and a large range in 207Pb/204Pb. Geochemical and isotopicrelationships are most compatible with remelting of hybridizedlithospheric mantle generated during arc-continent collision.A genetic link is suggested among collision-related delaminationor slab break-off events and emplacement of ‘post-erogenic’granite suites. A-type granites may recycle previously subductedcontinental material, and help explain the mass balance notedfor modern arcs. However, they need not represent net, new,crustal growth. KEY WORDS: A-type granites; juvenile crust; isotopes; Newfoundland *Telephone: (613) 995-4972. Fax: (613) 995-7997. e-mail: jwhalen{at}gsc.emr.ca  相似文献   

20.
The Grønnedal-Ika complex is dominated by layered nephelinesyenites which were intruded by a xenolithic syenite and a centralplug of calcite to calcite–siderite carbonatite. Aegirine–augite,alkali feldspar and nepheline are the major mineral phases inthe syenites, along with rare calcite. Temperatures of 680–910°Cand silica activities of 0·28–0·43 weredetermined for the crystallization of the syenites on the basisof mineral equilibria. Oxygen fugacities, estimated using titanomagnetitecompositions, were between 2 and 5 log units above the fayalite–magnetite–quartzbuffer during the magmatic stage. Chondrite-normalized REE patternsof magmatic calcite in both carbonatites and syenites are characterizedby REE enrichment (LaCN–YbCN = 10–70). Calcite fromthe carbonatites has higher Ba (5490 ppm) and lower HREE concentrationsthan calcite from the syenites (54–106 ppm Ba). This isconsistent with the behavior of these elements during separationof immiscible silicate–carbonate liquid pairs. Nd(T =1·30 Ga) values of clinopyroxenes from the syenites varybetween +1·8 and +2·8, and Nd(T) values of whole-rockcarbonatites range from +2·4 to +2·8. Calcitefrom the carbonatites has 18O values of 7·8 to 8·6and 13C values of –3·9 to –4·6. 18Ovalues of clinopyroxene separates from the nepheline syenitesrange between 4·2 and 4·9. The average oxygenisotopic composition of the nepheline syenitic melt was calculatedbased on known rock–water and mineral–water isotopefractionation to be 5·7 ± 0·4. Nd and C–Oisotope compositions are typical for mantle-derived rocks anddo not indicate significant crustal assimilation for eithersyenite or carbonatite magmas. The difference in 18O betweencalculated syenitic melts and carbonatites, and the overlapin Nd values between carbonatites and syenites, are consistentwith derivation of the carbonatites from the syenites via liquidimmiscibility. KEY WORDS: alkaline magmatism; carbonatite; Gardar Province; liquid immiscibility; nepheline syenite  相似文献   

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