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1.
Experimental Constraints on the Role of Garnet Pyroxenite in the Genesis of High-Fe Mantle Plume Derived Melts 总被引:10,自引:1,他引:9
The anhydrous phase relations of an uncontaminated (primitive),ferropicrite lava from the base of the Early Cretaceous ParanáEtendekacontinental 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 olivineclinopyroxene residue, or at 5 GPawith a garnetclinopyroxene 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
2.
Petrology and Petrogenesis of Cumulate Peridotites and Gabbros from the Marum Ophiolite Complex, Northern Papua New Guinea 总被引:1,自引:0,他引:1
The Marum ophiolite complex in northern Papua New Guinea includesa thick (34 km) sequence of ultramafic and mafic cumulates,which are layered on a gross scale from dunite at the base upwardsthrough wehrlite, lherzolite, plagioclase lherzolite, pyroxenite,olivine norite-gabbro and norite-gabbro to anorthositic gabbroand ferrogabbro at the top. Igneous layering and structures,and cumulus textures indicate an origin by magmatic crystallizationin a large magma chamber(s) from magma(s) of evolving composition.Most rocks however show textural and mineralogical evidenceof subsolidus re-equilibration. The cumulate sequence is olivine and chrome spinel followedby clinopyroxene, orthopyroxene and plagioclase, and the layeredsequence is similar to that of the Troodos and Papuan ophiolites.These sequences differ from ophiolites such as Vourinos by thepresence of cumulus magnesian orthopyroxene, and are not consistentwith accumulation of low pressure liquidus phases of mid-oceanridge-type olivine tholeiite basalts. The cumulus phases show cryptic variation from Mg- and Ca-richearly cumulates to lower temperature end-members, e.g. olivineMg9378, plagioclase An9463. Co-existing pyroxenesdefine a high temperature solidus with a narrower miscibilitygap than that of pyroxenes from stratiform intrusions. Re-equilibratedpyroxene pairs define a low-temperature, subsolidus solvus.Various geothermometers and geobarometers, together with thermodynamiccalculations involving silica buffers, suggest the pyroxene-bearingcumulates crystallized at 1200 °C and 12 kb pressureunder low fO2. The underlying dunites and chromitites crystallizedat higher temperature, 13001350 °C. The bulk of thecumulates have re-equilibrated under subsolidus conditions:co-existing pyroxenes record equilibration temperatures of 850900°C whereas olivine-spinel and magnetite-ilmenite pairs indicatefinal equilibration at very low temperatures (600 °C). Magmas parental to the cumulate sequence are considered to havebeen of magnesian olivine-poor tholeiite composition (>50per cent SiO2, 15 per cent MgO, 100 Mg/(Mg + Fe2+) 78) richin Ni and Cr, and poor in TiO2 and alkalies. Fractionated examplesof this magma type occur at a number of other ophiolites withsimilar cumulate sequences. Experimental studies show that suchlavas may result from ial melting of depleted mantle lherzoliteat shallow depth. The tectonic environment in which the complexformed might have been either a mid-ocean ridge or a back-arebasin. 相似文献
3.
THOMPSON R. N.; OTTLEY C. J.; SMITH P. M.; PEARSON D. G.; DICKIN A. P.; MORRISON M. A.; LEAT P. T.; GIBSON S. A. 《Journal of Petrology》2005,46(8):1603-1643
The <80 ka basaltsbasanites of the Potrillo VolcanicField (PVF) form scattered scoria cones, lava flows and maarsadjacent to the New MexicoMexico border. MgO ranges upto 12·5%; lavas with MgO < 10·7% have fractionatedboth olivine and clinopyroxene. Cumulate fragments are commonin the lavas, as are subhedral megacrysts of aluminous clinopyroxene(with pleonaste inclusions) and kaersutitic amphibole. REE modellingindicates that these megacrysts could be in equilibrium withthe PVF melts at 1·61·7 GPa pressure. Thelavas fall into two geochemical groups: the Main Series (85%of lavas) have major- and trace-element abundances and ratiosclosely resembling those of worldwide ocean-island alkali basaltsand basanites (OIB); the Low-K Series (15%) differ principallyby having relatively low K2O and Rb contents. Otherwise, theyare chemically indistinguishable from the Main Series lavas.Sr- and Nd-isotopic ratios in the two series are identical andvary by scarcely more than analytical error, averaging 87Sr/86Sr= 0·70308 (SD = 0·00004) and 143Nd/144Nd = 0·512952(SD=0·000025). Such compositions would be expected ifboth series originated from the same mantle source, with Low-Kmelts generated when amphibole remained in the residuum. ThreePVF lavas have very low Os contents (<14 ppt) and appearto have become contaminated by crustal Os. One Main Series picritehas 209 ppt Os and has a Os value of +13·6, typical forOIB. This contrasts with published 187Os/188Os ratios for KilbourneHole peridotite mantle xenoliths, which give mostly negativeOs values and show that Proterozoic lithospheric mantle formsa thick Mechanical Boundary Layer (MBL) that extends to 70 kmdepth beneath the PVF area. The calculated mean primary magma,in equilibrium with Fo89, has Na2O and FeO contents that givea lherzolite decompression melting trajectory from 2·8GPa (95 km depth) to 2·2 GPa (70 km depth). Inverse modellingof REE abundances in Main Series Mg-rich lavas is successfulfor a model invoking decompression melting of convecting sub-lithosphericlherzolite mantle (Nd = 6·4; Tp 1400°C) between90 and 70 km. Nevertheless, such a one-stage model cannot accountfor the genesis of the Low-K Series because amphibole wouldnot be stable within convecting mantle at Tf 1400°C. Thesemagmas can only be accommodated by a three-stage model thatenvisages a Thermal Boundary Layer (TBL) freezing conductivelyonto the 70 km base of the Proterozoic MBL during the 20 Myrtectonomagmatic quiescence before PVF eruptions. As it grew,this was veined by hydrous small-fraction melts from below.The geologically recent arrival of hotter-than-ambient (Tp 1400°C) convecting mantle beneath the Potrillo area re-meltedthe TBL and caused the magmatism. KEY WORDS: western USA; picrites; SrNdOs isotopes; petrogenetic modelling; thermal boundary layer 相似文献
4.
Partial Melting Experiments of Peridotite + CO2 at 3 GPa and Genesis of Alkalic Ocean Island Basalts
We document compositions of minerals and melts from 3 GPa partialmelting experiments on two carbonate-bearing natural lherzolitebulk compositions (PERC: MixKLB-1 + 2·5 wt% CO2; PERC3:MixKLB-1 + 1 wt% CO2) and discuss the compositions of partialmelts in relation to the genesis of alkalic to highly alkalicocean island basalts (OIB). Near-solidus (PERC: 1075–1105°C;PERC3: 1050°C) carbonatitic partial melts with <10 wt%SiO2 and 40 wt% CO2 evolve continuously to carbonated silicatemelts with >25 wt% SiO2 and <25 wt% CO2 between 1325 and1350°C in the presence of residual olivine, orthopyroxene,clinopyroxene, and garnet. The first appearance of CO2-bearingsilicate melt at 3 GPa is 150°C cooler than the solidusof CO2-free peridotite. The compositions of carbonated silicatepartial melts between 1350 and 1600°C vary in the rangeof 28–46 wt% SiO2, 1·6–0·5 wt% TiO2,12–10 wt% FeO*, and 19–29 wt% MgO for PERC, and42–48 wt% SiO2, 1·9–0·5 wt% TiO2,10·5–8·4 wt% FeO*, and 15–26 wt% MgOfor PERC3. The CaO/Al2O3 weight ratio of silicate melts rangesfrom 2·7 to 1·1 for PERC and from 1·7 to1·0 for PERC3. The SiO2 contents of carbonated silicatemelts in equilibrium with residual peridotite diminish significantlywith increasing dissolved CO2 in the melt, whereas the CaO contentsincrease markedly. Equilibrium constants for Fe*–Mg exchangebetween carbonated silicate liquid and olivine span a rangesimilar to those for CO2-free liquids at 3 GPa, but diminishslightly with increasing dissolved CO2 in the melt. The carbonatedsilicate partial melts of PERC3 at <20% melting and partialmelts of PERC at 15–33% melting have SiO2 and Al2O3 contents,and CaO/Al2O3 values, similar to those of melilititic to basaniticalkali OIB, but compared with the natural lavas they are moreenriched in CaO and they lack the strong enrichments in TiO2characteristic of highly alkalic OIB. If a primitive mantlesource is assumed, the TiO2 contents of alkalic OIB, combinedwith bulk peridotite/melt partition coefficients of TiO2 determinedin this study and in volatile-free studies of peridotite partialmelting, can be used to estimate that melilitites, nephelinites,and basanites from oceanic islands are produced from 0–6%partial melting. The SiO2 and CaO contents of such small-degreepartial melts of peridotite with small amounts of total CO2can be estimated from the SiO2–CO2 and CaO–CO2 correlationsobserved in our higher-degree partial melting experiments. Thesesuggest that many compositional features of highly alkalic OIBmay be produced by 1–5% partial melting of a fertile peridotitesource with 0·1–0·25 wt% CO2. Owing to verydeep solidi of carbonated mantle lithologies, generation ofcarbonated silicate melts in OIB source regions probably happensby reaction between peridotite and/or eclogite and migratingcarbonatitic melts produced at greater depths. KEY WORDS: alkali basalts; carbonated peridotite; experimental petrology; ocean island basalts; partial melting 相似文献
5.
GANGOPADHYAY AMITAVA; WALKER RICHARD J.; HANSKI EERO; SOLHEID PETER A. 《Journal of Petrology》2006,47(4):773-789
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. ReOsisotope 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 OsNd isotopic data limit the enrichmentprocess to within 200 Myr prior to the formation of the komatiites.Their OsNd 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
6.
TAPPE SEBASTIAN; FOLEY STEPHEN F.; JENNER GEORGE A.; HEAMAN LARRY M.; KJARSGAARD BRUCE A.; ROMER ROLF L.; STRACKE ANDREAS; JOYCE NANCY; HOEFS JOCHEN 《Journal of Petrology》2006,47(7):1261-1315
Numerous dykes of ultramafic lamprophyre (aillikite, mela-aillikite,damtjernite) and subordinate dolomite-bearing carbonatite withUPb perovskite emplacement ages of 590555 Ma occurin the vicinity of Aillik Bay, coastal Labrador. The ultramaficlamprophyres principally consist of olivine and phlogopite phenocrystsin a carbonate- or clinopyroxene-dominated groundmass. Ti-richprimary garnet (kimzeyite and Ti-andradite) typically occursat the aillikite type locality and is considered diagnosticfor ultramafic lamprophyrecarbonatite suites. Titanianaluminous phlogopite and clinopyroxene, as well as comparativelyAl-enriched but CrMg-poor spinel (Cr-number < 0.85),are compositionally distinct from analogous minerals in kimberlites,orangeites and olivine lamproites, indicating different magmageneses. The Aillik Bay ultramafic lamprophyres and carbonatiteshave variable but overlapping 87Sr/86Sri ratios (0·703690·70662)and show a narrow range in initial Nd (+0·1 to +1·9)implying that they are related to a common type of parentalmagma with variable isotopic characteristics. Aillikite is closestto this primary magma composition in terms of MgO (1520wt %) and Ni (200574 ppm) content; the abundant groundmasscarbonate has 13CPDB between 5·7 and 5,similar to primary mantle-derived carbonates, and 18OSMOW from9·4 to 11·6. Extensive melting of a garnet peridotitesource region containing carbonate- and phlogopite-rich veinsat 47 GPa triggered by enhanced lithospheric extensioncan account for the volatile-bearing, potassic, incompatibleelement enriched and MgO-rich nature of the proto-aillikitemagma. It is argued that low-degree potassic silicate to carbonatiticmelts from upwelling asthenosphere infiltrated the cold baseof the stretched lithosphere and solidified as veins, therebycrystallizing calcite and phlogopite that were not in equilibriumwith peridotite. Continued Late Neoproterozoic lithosphericthinning, with progressive upwelling of the asthenosphere beneatha developing rift branch in this part of the North Atlanticcraton, caused further veining and successive remelting of veinsplus volatile-fluxed melting of the host fertile garnet peridotite,giving rise to long-lasting hybrid ultramafic lamprophyre magmaproduction in conjunction with the break-up of the Rodinia supercontinent.Proto-aillikite magma reached the surface only after coatingthe uppermost mantle conduits with glimmeritic material, whichcaused minor alkali loss. At intrusion level, carbonate separationfrom this aillikite magma resulted in fractionated dolomite-bearingcarbonatites (13CPDB 3·7 to 2·7)and carbonate-poor mela-aillikite residues. Damtjernites maybe explained by liquid exsolution from alkali-rich proto-aillikitemagma batches that moved through previously reaction-lined conduitsat uppermost mantle depths. KEY WORDS: liquid immiscibility; mantle-derived magmas; metasomatism, SrNd isotopes; UPb geochronology 相似文献
7.
RILEY TEAL R.; LEAT PHILIP T.; CURTIS MICHAEL L.; MILLAR IAN. L.; DUNCAN ROBERT A.; FAZEL ADELA 《Journal of Petrology》2005,46(7):1489-1524
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 MgFe 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 TiO2Zr contents and are the most enriched magmagroup of the KarooAntarctic province, with ocean-islandbasalt (OIB)-like chemistry. Dykes of Group 1 and Group 3 aresub-parallel (ENEWSW) 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 NNESSW strike. KEY WORDS: flood basalt; depleted mantle; enriched mantle; Ahlmannryggen; Karoo dyke 相似文献
8.
Thermal History of the Horoman Peridotite Complex: A Record of Thermal Perturbation in the Lithospheric Mantle 总被引:1,自引:0,他引:1
The ascent history of the Horoman peridotite complex, Hokkaido,northern Japan, is revised on the basis of a detailed studyof large ortho- and clinopyroxene grains 1 cm in size (megacrysts)in the Upper Zone of the complex. The orthopyroxene megacrystsexhibit distinctive M-shaped Al zoning patterns, which werenot observed in porphyroclastic grains less than 5 mm in sizedescribed in previous studies. Moreover, the Al and Ca contentsof the cores of the orthopyroxene megacrysts are lower thanthose of the porphyroclasts. The Upper Zone is inferred to haveresided not only at a higher temperature than previously suggestedbut also at a higher pressure (1070°C, 2·3 GPa) thanthe Lower Zone (950°C, 1·9 GPa), in the garnet stabilityfield, before the ascent of the two zones. The Horoman complexprobably represents a 12 ± 5 km thick section of lithosphericmantle with an 10 ± 8°C/km vertical thermal gradient.The current thickness of the Horoman complex is 3 km, whichis a result of shortening of the lithospheric mantle by 0·25± 0·1 during its ascent. The Upper Zone appearsto have experienced a heating event during its ascent throughthe spinel stability field, with a peak temperature as highas 1200°C. The effect of heating decreases continuouslytowards the base of the complex, and the lowermost part of theLower Zone underwent very minor heating at a pressure higherthan 0·5 GPa. The uplift and associated deformation,as well as heating, was probably driven by the ascent of a hotasthenospheric upper-mantle diapir into the Horoman lithosphere. KEY WORDS: Horoman; PT trajectory; thermal history; Al diffusion in pyroxene; geothermobarometry 相似文献
9.
Phase Equilibria Constraints on the Chemical and Physical Evolution of the Campanian Ignimbrite 总被引:5,自引:1,他引:4
Fowler Sarah J.; Spera Frank J.; Bohrson Wendy A.; Belkin Harvey E.; De Vivo Benedetto 《Journal of Petrology》2007,48(3):459-493
The Campanian Ignimbrite is a > 200 km3 trachytephonolitepyroclastic deposit that erupted at 39·3 ± 0·1ka within the Campi Flegrei west of Naples, Italy. Here we testthe hypothesis that Campanian Ignimbrite magma was derived byisobaric crystal fractionation of a parental basaltic trachyandesiticmelt that reacted and came into local equilibrium with smallamounts (510 wt%) of crustal rock (skarns and foid-syenites)during crystallization. Comparison of observed crystal and magmacompositions with results of phase equilibria assimilationfractionationsimulations (MELTS) is generally very good. Oxygen fugacitywas approximately buffered along QFM + 1 (where QFM is the quartzfayalitemagnetitebuffer) during isobaric fractionation at 0·15 GPa ( 6km depth). The parental melt, reconstructed from melt inclusionand host clinopyroxene compositions, is found to be basaltictrachyandesite liquid (51·1 wt% SiO2, 9·3 wt%MgO, 3 wt% H2O). A significant feature of phase equilibria simulationsis the existence of a pseudo-invariant temperature, 883 °C,at which the fraction of melt remaining in the system decreasesabruptly from 0·5 to < 0·1. Crystallizationat the pseudo-invariant point leads to abrupt changes in thecomposition, properties (density, dissolved water content),and physical state (viscosity, volume fraction fluid) of meltand magma. A dramatic decrease in melt viscosity (from 1700Pa s to 200 Pa s), coupled with a change in the volume fractionof water in magma (from 0·1 to 0·8) and a dramaticdecrease in melt and magma density acted as a destabilizingeruption trigger. Thermal models suggest a timescale of 200kyr from the beginning of fractionation until eruption, leadingto an apparent rate of evolved magma generation of about 103km3/year. In situ crystallization and crystal settling in density-stratifiedregions, as well as in convectively mixed, less evolved subjacentmagma, operate rapidly enough to match this apparent volumetricrate of evolved magma production. KEY WORDS: assimilation; Campanian Ignimbrite; fractional crystallization; magma dynamics; phase equilibria 相似文献
10.
This study reports oxygen isotope ratios determined by laserfluorination of mineral separates (mainly plagioclase) frombasaltic andesitic to rhyolitic composition volcanic rocks eruptedfrom the Lassen Volcanic Center (LVC), northern California.Plagioclase separates from nearly all rocks have 18O values(6·1–8·4) higher than expected for productionof the magmas by partial melting of little evolved basalticlavas erupted in the arc front and back-arc regions of the southernmostCascades during the late Cenozoic. Most LVC magmas must thereforecontain high 18O crustal material. In this regard, the 18O valuesof the volcanic rocks show strong spatial patterns, particularlyfor young rhyodacitic rocks that best represent unmodified partialmelts of the continental crust. Rhyodacitic magmas erupted fromvents located within 3·5 km of the inferred center ofthe LVC have consistently lower 18O values (average 6·3± 0·1) at given SiO2 contents relative to rockserupted from distal vents (>7·0 km; average 7·1± 0.1). Further, magmas erupted from vents situated attransitional distances have intermediate values and span a largerrange (average 6·8 ± 0·2). Basaltic andesiticto andesitic composition rocks show similar spatial variations,although as a group the 18O values of these rocks are more variableand extend to higher values than the rhyodacitic rocks. Thesefeatures are interpreted to reflect assimilation of heterogeneouslower continental crust by mafic magmas, followed by mixingor mingling with silicic magmas formed by partial melting ofinitially high 18O continental crust (9·0) increasinglyhybridized by lower 18O (6·0) mantle-derived basalticmagmas toward the center of the system. Mixing calculationsusing estimated endmember source 18O values imply that LVC magmascontain on a molar oxygen basis approximately 42 to 4% isotopicallyheavy continental crust, with proportions declining in a broadlyregular fashion toward the center of the LVC. Conversely, the18O values of the rhyodacitic rocks suggest that the continentalcrust in the melt generation zones beneath the LVC has beensubstantially modified by intrusion of mantle-derived basalticmagmas, with the degree of hybridization ranging on a molaroxygen basis from approximately 60% at distances up to 12 kmfrom the center of the system to 97% directly beneath the focusregion. These results demonstrate on a relatively small scalethe strong influence that intrusion of mantle-derived maficmagmas can have on modifying the composition of pre-existingcontinental crust in regions of melt production. Given thisresult, similar, but larger-scale, regional trends in magmacompositions may reflect an analogous but more extensive processwherein the continental crust becomes progressively hybridizedbeneath frontal arc localities as a result of protracted intrusionof subduction-related basaltic magmas. KEY WORDS: oxygen isotopes; phenocrysts; continental arc magmatism; Cascades; Lassen 相似文献
11.
Liquidus relations in the four-component system Na2OAl2O3SiO2F2O1were studied at 0· 1 and 100 MPa to define the locationof fluoridesilicate liquid immiscibility and outlinedifferentiation paths of fluorine-bearing silicic magmas. Thefluoridesilicate liquid immiscibility spans the silicaalbitecryoliteand silicatopazcryolite ternaries and the haplogranite-cryolitebinary at greater than 960°C and 0· 1100 MPa.With increasing Al2O3 in the system and increasing aluminum/alkalication ratio, the two-liquid gap contracts and migrates fromthe silica liquidus to the cryolite liquidus. The gap does notextend to subaluminous and peraluminous melt compositions. Forall alkali feldsparquartz-bearing systems, the miscibilitygap remains located on the cryolite liquidus and is thus inaccessibleto differentiating granitic and rhyolitic melts. In peralkalinesystems, the magmatic differentiation is terminated at the albitequartzcryoliteeutectic at 770°C, 100 MPa, 5 wt % F and cation Al/Na =0· 75. The addition of topaz, however, significantlylowers melting temperatures and allows strong fluorine enrichmentin subaluminous compositions. At 100 MPa, the binary topazcryoliteeutectic is located at 770°C, 39 wt % F, cation Al/Na 0·95, and the ternary quartztopazcryolite eutecticis found at 740°C, 32 wt % F, 30 wt % SiO2 and cation Al/Na 0· 95. Such location of both eutectics enables fractionationpaths of subaluminous quartz-saturated systems to produce fluorine-rich,SiO2-depleted and nepheline-normative residual liquids. KEY WORDS: silicate melt; granite; rhyolite; fluorine; liquid immiscibility 相似文献
12.
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/650700°Cand 1·0 ± 0·1 GPa/620650°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/620650°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/620630°C;that is, over a depth range of 4560 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
13.
Marbles and metapelites from the Reynolds Range Group (centralAustralia) were regionally metamorphosed at low pressure duringM2 at 1.6 Ga, M2 ranged in grade from greenschist to granulitefacies along the length of the Reynolds Range, and overprinted1.78 Ga granites and their contact aureoles in the ReynoldsRange Group metasediments. At all M2 grades the marbles andmetapelites have highly variable oxygen isotope ratios [marbles:18O(carb) 1420%; metapelites: 18O 614%). Similarly, 1.78 Ga granites have highly variable oxygen isotope ratios(18O 513%), with the lowest values occurring at thegranite margins. In all rock types, the lowest oxygen isotopevalues are consistent with the infiltration of channelled magmaticand/or meteoric fluids. The variable lowering of oxygen isotopevalues resulted from pre-M2 contact metamorphism and fluidrockinteraction around the 1.78 Ga granites. In contrast, mineralassemblages in the marbles define a trend of increasing XCO2with increasing grade from <0.05 (greenschist facies) to0.71.0 (granulite facies). This, together with the lackof regionally systematic resetting of oxygen isotope ratios,implies that there was little fluidrock interaction duringprograde regional metamorphism. KEY WORDS: low pressure; polymetamorphism; fluids; stable isotopes; petrology
*Corresponding author Fax: 61394791272. e-mail: geoisb{at}lure.latrobe.edu.au 相似文献
14.
Pan-African high-grade metamorphism in the Kerala KhondaliteBelt (South India) led to the in situ formation of garnet-bearingleucosomes (L1) in sodic quartzalkali feldsparbiotitegneisses. Microtextures, mineralogy and the geochemical characteristicsof in situ leucosomes (L1) and gneiss domains (GnD) indicatethat the development of leucosomes was mainly controlled bythe growth of garnet at the expense of biotite. This is documentedby the selective transfer of FeO, MgO, , Sm and the heavy rareearth elements into the L1 domains. P-T constraints (T>800C,P>6kbar, aH2O0.3) suggest that the leucosomes were formedthrough complete melting of biotite in fluid-absent conditions,following the model reaction Biotite+Alkali feldspar+QuartzlGarnet+Ilmenite+Melt.The fraction of melt generated during this process was low (<10vol.%). The identical size of the leucosomes as well as theirhomogeneous and isotropic distribution at outcrop scale, whichlacks any evidence for melt segregation, suggest that the migmatiteremained a closed system. Subsequent to migmatization, the leptyniticgneisses were intruded by garnet-bearing leucogranitic melts(L2), forming veins parallel and subperpendicular to the foliation.The leucogranites are rich in potassium (K2O5.5 wt%), (Ba400p.p.m.) and Sr (300 p.p.m.), and exhibit low concentrationsof Zr (40 p.p.m.), Th (<1 p.p.m.) and (<10 p.p.m.). Thechondrite-normalized REE spectra show low abundances (LaN20,LuN3) and are moderately fractionated (LaN/LuN7). An Eu anomalyis absent or weakly negative. The higher 87Sr/86Sr ratio at550 Ma (0.7345) compared with the migmatite (0.7164) precludesa direct genetic relationship between leptynitic gneisses andleucogranites at Manali.Nevertheless, the chemical and mineralogicalcompositions of the leuocogranites strongly favour a derivationthrough fluid-absent biotite melting of isotopically distinctbut chemically comparable Manali-type gneisses. The undersaturationof Zr, Th and REE, a typical feature of leucogranitic meltsgenerated during granulite facies anatexis of psammo-peliticlithologies and attributed to disequilibrium melting with incompletedissolution of accessory phases (zircon, monazite), is weaklydeveloped in the leucogranites of Manali.It is concluded thatthis is mainly due to the sluggish migration of the melts instatic conditions, which facilitated equilibration with therestitic gneisses.
*Fax: 0228-732763; e-mail: ingo.braun{at}uni-bonn.de 相似文献
15.
We explore the partial melting behavior of a carbonated silica-deficienteclogite (SLEC1; 5 wt % CO2) from experiments at 3 GPa and comparethe compositions of partial melts with those of alkalic andhighly alkalic oceanic island basalts (OIBs). The solidus islocated at 10501075 °C and the liquidus at 1415 °C.The sub-solidus assemblage consists of clinopyroxene, garnet,ilmenite, and calcio-dolomitic solid solution and the near solidusmelt is carbonatitic (<2 wt % SiO2, <1 wt % Al2O3, and<0·1 wt % TiO2). Beginning at 1225 °C, a stronglysilica-undersaturated silicate melt (3443 wt % SiO2)with high TiO2 (up to 19 wt %) coexists with carbonate-richmelt (<5 wt % SiO2). The first appearance of carbonated silicatemelt is 100 °C cooler than the expected solidus of CO2-freeeclogite. In contrast to the continuous transition from carbonateto silicate melts observed experimentally in peridotite + CO2systems, carbonate and silicate melt coexist over a wide temperatureinterval for partial melting of SLEC1 carbonated eclogite at3 GPa. Silicate melts generated from SLEC1, especially at highmelt fraction (>20 wt %), may be plausible sources or contributingcomponents to melilitites and melilititic nephelinites fromoceanic provinces, as they have strong compositional similaritiesincluding their SiO2, FeO*, MgO, CaO, TiO2 and Na2O contents,and CaO/Al2O3 ratios. Carbonated silicate partial melts fromeclogite may also contribute to less extreme alkalic OIB, asthese lavas have a number of compositional attributes, suchas high TiO2 and FeO* and low Al2O3, that have not been observedfrom partial melting of peridotite ± CO2. In upwellingmantle, formation of carbonatite and silicate melts from eclogiteand peridotite source lithologies occurs over a wide range ofdepths, producing significant opportunities for metasomatictransfer and implantation of melts. KEY WORDS: carbonated eclogite; experimental phase equilibria; partial melting; liquid immiscibility; ocean island basalts 相似文献
16.
Exhumation History of a Garnet Pyroxenite-bearing Mantle Section from a Continent-Ocean Transition (Northern Apennine Ophiolites, Italy) 总被引:3,自引:0,他引:3
Garnet clinopyroxenite and garnet websterite layers occur locallywithin mantle peridotite bodies from the External Liguride Jurassicophiolites (Northern Apennines, Italy). These ophiolites werederived from an oceancontinent transition similar tothe present-day western Iberian margin. The garnet clinopyroxenitesare mafic rocks with a primary mineral assemblage of pyrope-richgarnet + sodic Al-augite (Na2O 2·5 wt %, Al2O3 12·5wt %), with accessory graphite, FeNi sulphides and rutile.Decompression caused Na-rich plagioclase (An5045) exsolutionin clinopyroxene porphyroclasts and extensive development ofsymplectites composed of secondary orthopyroxene + plagioclase(An8572) + Al-spinel ± clinopyroxene ±ilmenite at the interface between garnet and primary clinopyroxene.Further decompression is recorded by the development of an olivine+ plagioclase-bearing assemblage, locally under syn-kinematicconditions, at the expense of two-pyroxenes + Al-spinel. Mg-richgarnet has been also found in the websterite layers, which arecommonly characterized by the occurrence of symplectites madeof orthopyroxene + Al-spinel ± clinopyroxene. The enclosingperidotites are Ti-amphibole-bearing lherzolites with a fertilegeochemical signature and a widespread plagioclase-facies myloniticfoliation, which preserve in places a spinel tectonite fabric.LuHf and SmNd mineral isochrons (220 ±13 Ma and 186.0 ± 1·8 Ma, respectively) have beenobtained from a garnet clinopyroxenite layer and interpretedas cooling ages. Geothermobarometric estimates for the high-pressureequilibration have yielded T 1100°C and P 2·8 GPa.The early decompression was associated with moderate cooling,corresponding to T 950°, and development of a spinel tectonitefabric in the lherzolites. Further decompression associatedwith plagioclaseolivine growth in both peridotites andpyroxenites was nearly isothermal. The shallow evolution occurredunder a brittle regime and led to the superposition of hornblendeto serpentine veining stages. The garnet pyroxenite-bearingmantle from the External Liguride ophiolites represents a raretectonic sampling of deep levels of subcontinental lithosphereexhumed in an oceanic setting. The exhumation was probably accomplishedthrough a two-step process that started during Late Palaeozoiccontinental extension. The low-pressure portion of the exhumationpath, probably including also the plagioclase mylonitic shearzones, was related to the Mesozoic (Triassic to Jurassic) riftingthat led to continental break-up. In Jurassic times, the studiedmantle sequence became involved in an extensional detachmentprocess that resulted in sea-floor denudation. KEY WORDS: garnet pyroxenite; ophiolite; non-volcanic margin; mantle exhumation; SmNd and LuHf geochronology 相似文献
17.
Mount Galunggung is a historically active volcano in southwesternJava that has erupted four times in the last two centuries.During the most recent event, which occurred during a 9monthinterval in 1982 83, some 305 106 m3 of mediumK,calcalkaline magma was erupted. This eruption was unusualbecause of its duration, the diversity of eruption dynamicsand products, and the range of lava compositions produced. Thecomposition of juvenile material changed gradually during thecourse of the eruption from initial plagioclase (An6075)and twopyrozene bearing andesites with 58% SiO2 to finalplagioclase (An8590), diopside, and olivine (Fo8590)bearing primitive magnesium basalts with 47% SiO2 Mineralogicaland compositional relationships indicate a magmatic evolutioninvolving differentitation of highMg parental melt. Theeruptive volumes of 35 106 m3 andesite, 120 106 m3 maficandesite, and 150 106 m3 basalt are consistent with the ideathat the 1982 83 eruption progressively tapped and draineda magma chamber that had become chemically stratified throughextensive crystal fractionation. Separates of plagioclase and pyroxene have 18O( SMO W) rangesof + 5. 6 to + 6.0 and + 5.3 to + 5.6, respectively, with 18Oplagpxvalues of + 0.4 to + 0.6o, indicating internal Oisotopeequiliburium at temperature of 1100850 C. The magenesianbasalts have magmatic 18O/ 16O ratios similar to those of midoceanridge basalt, and the Oisotope ratios of compositionallyevolved derivative melts show no evidence for contaminationof the galunggung magmas by 18Orich crust during differentiation.Andesites and transitional mafic and sites have a more variableOisotope character, with laves and phenocrysts havingboth higher and lower 18O values than observed in the parentalmagnesium basalts. These features are interpreted to reflectintramagma chamber processes affecting the upper portions ofthe differentiating Galunggung magma body before the 198283eruption. 相似文献
18.
Zircon Hf Isotopic Evidence for Mixing of Crustal and Silicic Mantle-derived Magmas in a Zoned Granite Pluton, Eastern Australia 总被引:3,自引:0,他引:3
Zircon Hf isotopic data from a zoned pluton of the Moonbi supersuite,New England batholith, eastern Australia, are consistent withmagma mixing between two silicic melts, each derived from isotopicallydistinct sources. Although zircons from three zones within theWalcha Road pluton give a U–Pb crystallization age of249 ± 3 Ma, zircon populations from each zone have arange in Hf. Zircons from the mafic hornblende–biotitemonzogranite pluton margin and intermediate zones have Hf +5to +11, whereas those from the more felsic centre of the plutonhave Hf +7 to +16, representing a total variation of 11 Hfunits. The Lu–Hf depleted mantle model ages range from650 to 250 Ma, with the younger zircons present only in thefelsic pluton centre. The variation in Hf indicates the involvementof silicic melts from at least two sources, one a crustal componentwith a Neoproterozoic model age and the other a primitive mantle-derivedcomponent with model ages similar to the U–Pb crystallizationage of the pluton. The zircons reflect the isotopic compositionsof the different proportions of crustal-derived silicic melt,relative to mantle-derived silicic melt, between melt generationand final pluton construction. The Walcha Road pluton is consideredto have formed by incremental assembly of progressively morefelsic melt batches resulting from mixing, replenishment andcrystal–melt separation, with final pluton constructioninvolving mechanical concentration as zones of crystal mush.The zoned pluton and, more broadly, the Moonbi supersuite provideexamples of magma mixing by which the more silicic units havemore juvenile isotopic compositions as a result of increasingproportions of residual melt from basalt fractionation, relativeto crustal partial melt. KEY WORDS: Australia; granite magma mixing; zircon; zoned pluton; Hf isotopes 相似文献
19.
The Gronnedal-Ika Carbonatite-Syenite Complex, South Greenland: Carbonatite Formation by Liquid Immiscibility 总被引:1,自引:0,他引:1
HALAMA RALF; VENNEMANN TORSTEN; SIEBEL WOLFGANG; MARKL GREGOR 《Journal of Petrology》2005,46(1):191-217
The Grønnedal-Ika complex is dominated by layered nephelinesyenites which were intruded by a xenolithic syenite and a centralplug of calcite to calcitesiderite carbonatite. Aegirineaugite,alkali feldspar and nepheline are the major mineral phases inthe syenites, along with rare calcite. Temperatures of 680910°Cand silica activities of 0·280·43 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 fayalitemagnetitequartzbuffer during the magmatic stage. Chondrite-normalized REE patternsof magmatic calcite in both carbonatites and syenites are characterizedby REE enrichment (LaCNYbCN = 1070). Calcite fromthe carbonatites has higher Ba (5490 ppm) and lower HREE concentrationsthan calcite from the syenites (54106 ppm Ba). This isconsistent with the behavior of these elements during separationof immiscible silicatecarbonate 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 rockwater and mineralwater isotopefractionation to be 5·7 ± 0·4. Nd and COisotope 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
20.
Simon Nina S. C.; Carlson Richard W.; Pearson D. Graham; Davies Gareth R. 《Journal of Petrology》2007,48(3):589-625
A detailed petrological and geochemical study of low-temperatureperidotite xenoliths from Kimberley and northern Lesotho ispresented to constrain the processes that led to the magmaphileelement depletion of the Kaapvaal cratonic lithospheric mantleand its subsequent re-enrichment in Si and incompatible traceelements. Whole-rocks and minerals have been characterized forReOs isotope compositions, and major and trace elementconcentrations, and garnet and clinopyroxene for LuHfand SmNd isotope compositions. Most samples are characterizedby Archaean Os model ages, low Al, Fe and Ca contents, highMg/Fe, low Re/Os, very low (< 0·1 x chondrite) heavyrare earth element (HREE) concentrations and a decoupling betweenNd and Hf isotope ratios. These features are most consistentwith initial melting at 3·2 Ga followed by metasomatismby hydrous fluids, which may have also caused additional meltingto produce a harzburgitic residue. The low HREE abundances ofthe peridotites require that extensive melting occurred in thespinel stability field, possibly preceded by some melting inthe presence of garnet. Fractional melting models suggest that30% melting in the spinel field or 20% melting in the garnetfield followed by 20% spinel-facies melting are required toexplain the most melt-depleted samples. Garnet NdHf isotopecharacteristics indicate metasomatic trace element enrichmentduring the Archaean. We therefore suggest a model includingshallow ridge melting, followed by metasomatism of the Kaapvaalupper mantle in subduction zones surrounding cratonic nuclei,probably during amalgamation of smaller pre-existing terranesin the Late Archaean (2·9 Ga). The fluid-metasomatizedresidua have subsequently undergone localized silicate meltinfiltration that led to clinopyroxene ± garnet enrichment.Calculated equilibrium liquids for clinopyroxene and their HfNdisotope compositions suggest that most diopside in the xenolithscrystallized from an infiltrating kimberlite-like melt, eitherduring Group II kimberlite magmatism at 200110 Ma (Kimberley),or shortly prior to eruption of the host kimberlite around 90Ma (northern Lesotho). KEY WORDS: Kaapvaal craton; lithospheric mantle; metasomatism; NdHf isotopes; ReOs isotopes 相似文献