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1.
Geochemical data from back-arc volcanic zones in the Manus Basinare used to define five magma types. Closest to the New Britainarc are medium-K lavas of the island arc association and back-arcbasin basalts (BABB). Mid-ocean ridge basalts (MORB), BABB andmildly enriched T-MORB (transitional MORB) occur along the ManusSpreading Center (MSC) and Extensional Transform Zone (ETZ).The MSC also erupted extreme back-arc basin basalts (XBABB),enriched in light rare earth elements, P, and Zr. Compared withnormal MORB, Manus MORB are even more depleted in high fieldstrength elements and slightly enriched in fluid-mobile elements,indicating slight, prior enrichment of their source with subduction-relatedcomponents. Chemical variations and modeling suggest systematic,coupled relationships between extent of mantle melting, priordepletion of the mantle source, and enrichment in subduction-relatedcomponents. Closest to the arc, the greatest addition of subduction-relatedcomponents has occurred in the mantle with the greatest amountof prior depletion, which has melted the most. Variations inK2O/H2O indicate that the subduction-related component is bestdescribed as a phlogopite and/or K-amphibole-bearing hybridizedperidotite. Magmas from the East Manus Rifts are enriched inNa and Zr with radiogenic 87Sr/86Sr, possibly indicating crustalinteraction in a zone of incipient rifting. The source for XBABBand lavas from the Witu Islands requires a mantle componentsimilar to carbonatite melt. KEY WORDS: Manus back-arc basin, mantle metasomatism, magma generation  相似文献   

2.
The compatibility of vanadium (V) during mantle melting is a function of oxygen fugacity (fO2): at high fO2’s, V becomes more incompatible. The prospects and limitations of using the V content of peridotites as a proxy for paleo-fO2 at the time of melt extraction were investigated here by assessing the uncertainties in V measurements and the sensitivity of V as a function of degree of melt extracted and fO2. V-MgO and V-Al2O3 systematics were found to be sensitive to fO2 variations, but consideration of the uncertainties in measurements and model parameters indicates that V is sensitive only to relative fO2 differences greater than ∼2 log units. Post-Archean oceanic mantle peridotites, as represented by abyssal peridotites and obducted massif peridotites, have V-MgO and -Al2O3 systematics that can be modeled by 1.5 GPa melting between FMQ − 3 and FMQ − 1. This is consistent with fO2’s of the mantle source for mid-ocean ridge basalts (MORBs) as determined by the Fe3+ activity of peridotitic minerals and basaltic glasses. Some arc-related peridotites have slightly lower V for a given degree of melting than oceanic mantle peridotites, and can be modeled by 1.5 GPa melting at fO2’s as high as FMQ. However, the majority of arc-related peridotites have V-MgO systematics overlapping that of oceanic mantle peridotites, suggesting that although some arc mantle may melt under slightly oxidizing conditions, most arc mantle does not. The fact that thermobarometrically determined fO2’s in arc peridotites and lavas can be significantly higher than that inferred from V systematics, suggests that V retains a record of the fO2 during partial melting, whereas the activity of Fe3+ in arc peridotitic minerals and lavas reflect subsequent metasomatic overprints and magmatic differentiation/emplacement processes, respectively.Peridotites associated with middle to late Archean cratonic mantle are characterized by highly variable V-MgO systematics. Tanzanian cratonic peridotites have V systematics indistinguishable from post-Archean oceanic mantle and can be modeled by 3 GPa partial melting at ∼FMQ − 3. In contrast, many South African and Siberian cratonic peridotites have much lower V contents for a given degree of melting, suggesting at first glance that partial melting occurred at high fO2’s. More likely, however, their unusually low V contents for a given degree of melting may be artifacts of excess orthopyroxene, a feature that pervades many South African and Siberian peridotites but not the Tanzanian peridotites. This is indicated by the fact that the V contents of South African and Siberian peridotites are correlated with increases in SiO2 content, generating data arrays that cannot be modeled by partial melting but can instead be generated by the addition of orthopyroxene through processes unrelated to primary melt depletion. Correction for orthopyroxene addition suggests that the South African and Siberian peridotites have V-MgO systematics similar to those of Tanzanian peridotites. Thus, if the Tanzanian peridotites represent the original partial melting residues, and if the South African and Siberian peridotites have been modified by orthopyroxene addition, then there is no indication that Archean cratonic mantle formed under fO2’s significantly greater than that of modern oceanic mantle. Instead, the fO2’s inferred from the V systematics in these three cratonic peridotite suites are within range of modern oceanic mantle. This also suggests that the transition from a highly reducing mantle in equilibrium with a metallic core to the present oxidized state must have occurred by late Archean times.  相似文献   

3.
Fluids or melts derived from a subducting plate are often citedas a mechanism for the oxidation of arc magmas. What remainsunclear is the link between the fluid, oxygen fugacity, andother major and trace components, as well as the spatial distributionof the impact of those fluids. To test the potential effectsof addition of a subduction-derived fluid or melt to the sub-arcmantle, olivine-hosted melt inclusions from primitive basalticlavas sampled from across the central Oregon Cascades (43°–45°N)have been analyzed for major, trace and volatile elements andfO2. Oxygen fugacity was determined in melt inclusions fromsulfur speciation determined by electron microprobe and fromolivine–chromite oxygen geobarometry. The overall rangein fO2 based on sulfur speciation measurements is from <–0·25log units to + 1·9 log units (FMQ, where FMQ is fayalite–magnetite–quartzbuffer). Oxygen fugacity is positively correlated with fluid-mobiletrace element and light rare earth element contents in basaltsgenerated by relatively low-degree partial melting. Establishinga further correlation between fO2 and fluid-mobile trace elementabundances with position along the arc requires the basaltsto be subdivided into shoshonitic, calc-alkaline, low-K tholeiiteand enriched intraplate basalt groups. Melt inclusions fromenriched intraplate and shoshonitic lavas show increasing fO2and trace element abundances closer to the trench, whereas calc-alkalinemelt inclusions exhibit no significant across-arc variations.Low-K tholeiitic melt inclusions record an increase in incompatibletrace elements closer to the trench; however, there is no correlatedincrease in fO2. The correlation observed in enriched intraplateand shoshonitic melt inclusions is interpreted to reflect aprogressively greater proportion of a fluid-rich, oxidized subductioncomponent in magmas generated nearer the subduction zone. Significantly,calc-alkaline melt inclusions with high ratios of large ionlithophile elements to high field strength elements, characteristicof ‘typical’ arc magmas, have oxidation states indistinguishablefrom low-K tholeiite and enriched intraplate basalt melt inclusions.The lack of across-arc geochemical variation in calc-alkalinemelt inclusions may suggest that these basalts are not necessarilythe most appropriate magmas for examining recent addition ofa subduction component to the sub-arc mantle. Flux and batchmelt model results produce a wide range of predicted amountsof melting and subduction component added to the mantle source;however, general trends characterized by increased melting andproportion of the subduction component from enriched intraplate,to low-K tholeiite, to calc-alkaline are robust. The model resultsdo not require enriched intraplate, low-K tholeiite and calc-alkalinemagmas to be produced from the same more fertile mantle source.However, enriched intraplate magmas, in contrast to calc-alkalineand low-K tholeiite magmas, cannot be generated from a depletedmantle source. Flux or batch melting of either the more fertileor depleted mantle sources used to generate the low-K tholeiite,calc-alkaline, and enriched intraplate magmas cannot reproduceshoshonitic compositions, which require a significantly depletedmantle source strongly metasomatized by a subduction component.The potential mantle source for shoshonitic basalts has a predictedfO2 (after oxidation) from + 0·3 to + 2·4 logunits (FMQ) whereas the mantle source for low-K tholeiite, calc-alkaline,and enriched intraplate magmas may range from –1·1to + 0·7 log units (FMQ). KEY WORDS: basalt; Cascades; melt inclusions; oxidation state; volatiles  相似文献   

4.
Quaternary lavas from the NE Japan arc show geochemical evidenceof mixing between mantle-derived basalts and crustal melts atthe magmatic front, whereas significant crustal signals arenot detected in the rear-arc lavas. The along-arc chemical variationsin lavas from the magmatic front are attributable almost entirelyto geochemical variations in the crustal melts that were mixedwith a common mantle-derived basalt. The mantle-derived basaltshave slightly enriched Sr–Pb and depleted Nd isotopiccompositions relative to the rear-arc lavas, but the variationis less pronounced if crustal contributions are eliminated.Therefore, the source mantle compositions and slab-derived fluxesare relatively uniform, both across and along the arc. Despitethis, incompatible element concentrations are significantlyhigher in the rear-arc basalts. We examine an open-system, fluid-fluxedmelting model, assuming that depleted mid-ocean ridge basalt(MORB)-source mantle melted by the addition of fluids derivedfrom subducted oceanic crust (MORB) and sediment (SED) hybridsat mixing proportions of 7% and 3% SED in the frontal- and rear-arcsources, respectively. The results reproduce the chemical variationsfound across the NE Japan arc with the conditions: 0·2%fluid flux with degree of melting F = 3% at 2 GPa in the garnetperidotite field for the rear arc, and 0·7% fluid fluxwith F = 20% at 1 GPa in the spinel peridotite field beneaththe magmatic front. The chemical process operating in the mantlewedge requires: (1) various SED–MORB hybrid slab fluidsources; (2) variable amounts of fluid; (3) a common depletedmantle source; (4) different melting parameters to explain across-arcchemical variations. KEY WORDS: arc magma; crustal melt; depleted mantle; NE Japan; Quaternary; slab fluid  相似文献   

5.
Mafic tholeiitic basalts from the Nejapa and Granada (NG) cindercone alignments provide new insights into the origin and evolutionof magmas at convergent plate margins. In comparison to otherbasalts from the Central American volcanic front, these marietholeiitic basalts are high in MgO and CaO and low in Al2Op,K2O1, Ba and Sr. They also differ from other Central Americanbasalts, in having clinopyroxene phenocrysts with higher MgO,CaO and Cr2O3 concentrations and olivine phenocrysts with higherMgO contents. Except for significantly higher concentrationsof Ba, Sr and 87Sr/86Sr, most of the tholeiites are indistinguishable in compositionfrom mid-ocean ridge basalts. In general, phenocryst mineralcompositions are also very similar between NG tholeiites andmid-ocean ridge basalts. The basalts as a whole can be dividedinto two groups based on relative TiO2-K2O concentrations. Thehigh-Ti basalts always have the lowest K2O and Ba and usuallyhave the highest Ni and Cr. All of the basalts have experienced some fractional crystallizationof olivine, plagioclase and clinopyroxene. Relative to otherCentral American basalts, the Nejapa-Granada basalts appearto have fractionated at low PT and PH2O. The source of primarymagmas for these basalts is the mantle wedge. Fluids and/ormelts may have been added to the mantle wedge from hydrothermally-altered,subducting oceanic crust in order to enrich the mantle in Sr,Ba and 87Sr/86Sr, but not in K and Rb. The role of lower crustaicontamination in causing the observed enrichments in Sr, Baand 87Sr/86Sr of NG basalts in comparison to mid-ocean ridgebasalts, however, is unclear. Rutile or a similar high-Ti accessoryphase may have been stable in the mantle source of the low-TiNG basalts, but not in that of the high-Ti basalts. Mafic tholeiiticbasalts, similar to those from Nejapa and Granada, may representmagmatic compositions parental to high-Al basalts, the mostmafic basalts at most Central American volcanoes. The characterof the residual high-Al basalts after this fractionation stepdepends critically on PH2O Both high and low-Ti andesites are also present at Nejapa. Likethe high-Ti basalts, the high-Ti andesites have lower K2O andBa and higher Ni and Cr in comparison to the low-Ti group. Thehigh-Ti andesites appear to be unrelated to any of the otherrocks and their exact origin is unknown. The low-Ti andesitesare the products of fractional crystallization of plagioclase,clinopyroxene, olivine (or orthopyroxene) and magnetite fromthe low-Ti basalts. The eruption that deposited a lapilli sectionat Cuesta del Plomo involved the explosive mixing of 3 components:high-Ti basaltic magma, low-Ti andesitic magma and high-Ti andesiticlava.  相似文献   

6.
The Antampombato–Ambatovy complex is the largest intrusionin the central–eastern part of the Cretaceous flood basaltprovince of Madagascar, with an exposed surface area of about80 km2. It has an 40Ar/39Ar incremental heating age of 89·9± 0·4 Ma and a U–Pb age of 90 ± 2Ma. The outcropping plutonic rocks range from dunite and wehrlite,through clinopyroxenite and gabbro, to sodic syenite. A dykeswarm cross-cutting some of the above lithologies (and the nearbyPrecambrian basement rocks) is formed of picritic basalts, alkalito transitional basalts, benmoreites and rhyolites; some ofthe latter are peralkaline. A few basaltic dykes have cumulateolivine textures, with up to 26 wt % MgO and 1200 ppm Ni, whereasothers have characteristics more akin to those of primitiveliquids (9 wt % MgO; Mg-number 0·61; 500 ppm Cr; 200ppm Ni). These basalts have relatively high TiO2 (2·2wt %) and total iron (14 wt % as Fe2O3), and moderate contentsof Nb (10–11 ppm) and Zr (c. 100 ppm). Initial (at 90Ma) Sr- and Nd-isotope ratios of the clinopyroxenites and basaltdykes are 0·7030–0·7037 and 0·51290–0·51283,respectively. Syenites and peralkaline rhyolites have Sr- andNd-isotope ratios of 0·7037–0·7039 and 0·51271–0·51274,respectively. The data suggest derivation of the parental magmasfrom a time-integrated depleted mantle source, combined withsmall amounts of crustal contamination in the petrogenesis ofthe more evolved magmas. The isotopic compositions of the mafic–ultramaficrocks are most similar to those of the mid-ocean ridge basalt(MORB)-like igneous rocks of eastern Madagascar, and suggestthe existence of an isotopically ‘depleted’ componentin the source of the entire Madagascar province, even thoughthe Antampombato basalts are chemically unlike the lavas anddykes with the same depleted isotopic signature found in westernMadagascar. If this depleted component is plume-related, thissuggests that the plume has a broadly MORB-source mantle composition.The existence of isotopically more enriched magma types in theMadagascan province has several possible petrogenetic explanations,one of which could be the interaction of plume-related meltswith the deep lithospheric mantle beneath the island. KEY WORDS: geochronology; flood basalts; Antampombato–Ambatovy intrusion; Cretaceous; Madagascar  相似文献   

7.
Mantle xenoliths from Tenerife show evidence of metasomatismand recrystallization overprinting the effects of extensivepartial melting. The evidence includes: recrystallization ofexsolved orthopyroxene porphyroclasts highly depleted in incompatibletrace elements into incompatible-trace-element-enriched, poikiliticorthopyroxene with no visible exsolution lamellae; formationof olivine and REE–Cr-rich, strongly Zr–Hf–Ti-depletedclinopyroxene at the expense of orthopyroxene; the presenceof phlogopite; whole-rock CaO/Al2O3 >> 1 (Ca metasomatism) inrecrystallized rocks; and enrichment in incompatible elementsin recrystallized rocks, relative to rocks showing little evidenceof recrystallization. The ‘higher-than-normal’ degreeof partial melting that preceded the metasomatism probably resultsfrom plume activity during the opening of the Central AtlanticOcean. Sr–Nd isotopic compositions are closely similarto those of Tenerife basalts, indicating resetting from theexpected original mid-ocean ridge basalt composition by themetasomatizing fluids. Metasomatism was caused by silicic carbonatitemelts, and involved open-system processes, such as trappingof elements compatible with newly formed acceptor minerals,leaving residual fluids moving to shallower levels. The compositionsof the metasomatizing fluids changed with time, probably asa result of changing compositions of the melts produced in theCanary Islands plume. Spinel dunites and wehrlites representrocks where all, or most, orthopyroxene has been consumed throughthe metasomatic reactions. KEY WORDS: Canary Islands; Tenerife; mantle xenoliths; geochemistry; Ca metasomatism; open-system processes; lithosphere; ocean islands  相似文献   

8.
The Southwest Indian Ridge (SWIR) at 9–16°E and 52–53°Sis characterized by ultra-slow, oblique spreading and containsone of the few documented occurrences of pyroxenite veins associatedwith abyssal peridotites. The origin of these uncommon lithologiesis still debated. We present a detailed study (including electronmicroprobe and laser ablation inductively coupled plasma massspectrometry) of spinel websterites collected during Cruise162, Leg 9, of the R.V. Knorr. Rare earth element patterns inclinopyroxenes (Cpx) lead us to discard a possible origin ofthe pyroxenites as residues from partial melting of garnet pyroxenites(i.e. relics of a layered mantle protolith). Their compositionand cumulate texture (when not obscured by mylonitization relatedto emplacement on the seafloor) are better interpreted in termsof fractional crystallization from a basaltic melt at relativelyhigh pressure. Evidence for a high pressure of crystallizationincludes the lack of plagioclase in the cumulate assemblageand the high Al2O3 contents of the pyroxenes: up to 5 wt % inorthopyroxene (Opx) and up to 7 wt % in Cpx. These values areamong the highest reported for pyroxenes in a mid-ocean ridgesetting. Sub-solidus breakdown of spinel to plagioclase (nowaltered) is observed in one sample, providing a rough estimateof the final equilibration pressure of these cumulates, around0· 6–0· 7 GPa (plagioclase–spineltransition for a bulk pyroxenite composition). The inferredpyroxenite parent melts were close to equilibrium with the associatedresidual peridotites; some samples have a slightly evolved compositionin terms of the Mg-number [Mg/(Mg + total Fe)]. These parentalmelts had major and trace element compositions consistent witha mid-ocean ridge basalt (MORB) affinity, although they werenot rigorously identical to MORB. Among other characteristics,these melts were relatively depleted in highly incompatibleelements. We propose that they correspond to the latest, shallowest,incremental melt fractions produced during fractional decompressionmelting of a normal MORB (N-MORB) mantle source. These meltsexperienced fractional crystallization as soon as they segregatedfrom the peridotite matrix, moved upward, and crossed the lithosphere–asthenosphereboundary (defined here as the base of the conductive lid). Asa consequence, these shallow melt fractions produced beneathmid-ocean ridges did not fully mix with melt fractions producedand extracted at greater depths. Our study provides concreteevidence for the actuality of pyroxene crystallization in meltchannels beneath mid-ocean ridges at relatively high pressures,a process frequently invoked to account for the ‘pyroxeneparadox’ in MORB petrogenesis. KEY WORDS: abyssal pyroxenites; cumulates; lithospheric mantle; melt migration; Southwest Indian Ridge  相似文献   

9.
Mantle preconditioning may be defined as the extraction of smallmelt fractions from mantle asthenosphere during its flow tothe site of magma generation. Equations may be written for mantlepreconditioning, assuming that the mantle comprises enriched‘plums’ in a depleted matrix. The equations takeinto account variations in mass fraction of plums, the relativerate of melting of plums and matrix, the temperature and pressureof melt extraction, the mass fraction of melt extracted, theextent of chemical exchange between plums and matrix, and theefficiency of melt extraction. Monitoring mineralogical changesand variations in partition coefficients along the inferredP–T–t path of the mantle asthenosphere allows theequations to be correctly applied to the conditions under whichmelt extraction takes place. Numerical experiments demonstratethe influence of petrogenetic variables on the shape of meltextraction trajectories and provide new criteria for distinguishingbetween melt extraction and mixing as the cause of regionalgeochemical gradients. Representative examples of arc–back-arcsystems (Scotia), continental break-up (Afar) and plume–ridgeinteraction (Azores) indicate that the compositions of the mantlesources of mid-ocean ridge basalts and island arc basalts maybe determined, at least in part, by the melt extraction historiesof their asthenospheric sources. KEY WORDS: geochemical modelling; mantle flow; isotope ratios; trace elements  相似文献   

10.
Geological and geophysical evidence indicates that at least100 km of Archaean to Proterozoic lithospheric mantle has beenremoved from beneath large areas of eastern and southeasternChina during late Mesozoic to Cenozoic time. Mantle-derivedxenoliths in Tertiary basalts from several localities acrossthis region have been studied by X-ray fluorescence, electronmicroprobe and laser ablation microprobe–inductively coupledplasma-mass spectrometry to characterize this thinner lithosphere.Trace element patterns of clinopyroxenes in the peridotitesfrom southeastern China can be divided into four groups: fertilegarnet lherzolites, fertile spinel (± garnet) lherzolites,and depleted and enriched peridotites. The addition of Nb, Sr,light rare earth elements, but not of Ti and Zr, suggests ametasomatizing agent containing both H2O and CO2. This studyalso demonstrates that the negative Ti anomaly commonly observedin clinopyroxene from mantle peridotites cannot be balancedby the Ti in coexisting orthopyroxene, but can be explainedby small degrees of partial melting, using appropriate distributioncoefficients. Most of the peridotites from southeastern China,whether spinel or garnet facies, are highly fertile in termsof Al2O3 and CaO contents and mg-number; many resemble commonlyused primitive mantle compositions. Modelling of trace elementpatterns in clinopyroxene indicates that most spinel and garnetperidotites from the Nushan, Mingxi and Niutoushan localitiesexperienced less than 5%, and many less than 2%, partial melting.A few depleted spinel peridotites from Nushan, and all spinelperidotites from Mingxi, require 10–25% fractional partialmelting; almost all spinel peridotites from the Qilin localityshow evidence of higher degrees (6–25%) of fractionalpartial melting. At both Nushan and Mingxi, the more depletedcompositions occur in the upper part of the lithospheric mantle,which now is  相似文献   

11.
Crystallization of Chromite and Chromium Solubility in Basaltic Melts   总被引：6，自引：3，他引：6  
The equilibrium between chromite and melt has been determinedon four basalts at temperatures of 1200–1400?C over arange of oxygen fugacity (fo2) and pressures of 1 atm and 10kb. The Cr content of chromite-saturated melts at 1300?C and1 atm ranges from 0?05 wt.% Cr2O3 at a log fo2= –3 to1?4 wt.% at a log fo2=–12?8. The Cr2+/Cr3+ of melt increaseswith decreasing fo2 and is estimated by assuming a constantpartitioning of Cr3+ between chromite and melt at constant temperature.The estimated values of Cr2+/Cr3+ in the melt are at fo2 valuesof 4–5 orders of magnitude lower than the equivalent Fe2+/Fe3+values. The Cr/(Cr+Al) of chromite coexisting with melt at constanttemperature changes little with variation of fo2 below log fo2=–6.Five experiments at 10 kb indicate that Cr2O3 dissolved in themelt is slightly higher and the Cr/(Cr + Al) of coexisting chromiteis slightly lower than experiments at 1 atm pressure. Thus variationin total pressure cannot explain the large variations of Cr/(Cr+ Al) that are common to mid-ocean ridge basalt (MORB) chromite. Experiments on a MORB at 1 atm at fo2 values close to fayalite-magnetite-quartz(FMQ) buffer showed that the Al2O3 content of melt is highlysensitive to the crystallization or melting of plagioclase,and consequently coexisting chromite shows a large change inCr/(Cr + Al). It would appear, therefore, that mixing of a MORBmagma containing plagioclase with a hotter MORB magma undersaturatedin plagioclase may give rise to the large range of Cr/(Cr +Al) observed in some MORB chromite.  相似文献   

12.
Macquarie Island is an exposure above sea-level of part of thecrest of the Macquarie Ridge. The ridge marks the Australia–Pacificplate boundary south of New Zealand, where the plate boundaryhas evolved progressively since Eocene times from an oceanicspreading system into a system of long transform faults linkedby short spreading segments, and currently into a right-lateralstrike-slip plate boundary. The rocks of Macquarie Island wereformed during spreading at this plate boundary in Miocene times,and include intrusive rocks (mantle and cumulate peridotites,gabbros, sheeted dolerite dyke complexes), volcanic rocks (N-to E-MORB pillow lavas, picrites, breccias, hyaloclastites),and associated sediments. A set of Macquarie Island basalticglasses has been analysed by electron microprobe for major elements,S, Cl and F; by Fourier transform infrared spectroscopy forH2O; by laser ablation–inductively coupled plasma massspectrometry for trace elements; and by secondary ion mass spectrometryfor Sr, Nd and Pb isotopes. An outstanding compositional featureof the data set (47·4–51·1 wt % SiO2, 5·65–8·75wt % MgO) is the broad range of K2O (0·1–1·8wt %) and the strong positive covariation of K2O with otherincompatible minor and trace elements (e.g. TiO2 0·97–2·1%;Na2O 2·4–4·3%; P2O5 0·08–0·7%;H2O 0·25–1·5%; La 4·3–46·6ppm). The extent of enrichment in incompatible elements in glassescorrelates positively with isotopic ratios of Sr (87Sr/86Sr= 0·70255–0·70275) and Pb (206Pb/204Pb =18·951–19·493; 207Pb/204Pb = 15·528–15·589;208Pb/204Pb = 38·523–38·979), and negativelywith Nd (143Nd/144Nd = 0·51310–0·51304).Macquarie Island basaltic glasses are divided into two compositionalgroups according to their mg-number–K2O relationships.Near-primitive basaltic glasses (Group I) have the highest mg-number(63–69), and high Al2O3 and CaO contents at a given K2Ocontent, and carry microphenocrysts of primitive olivine (Fo86–89·5).Their bulk compositions are used to calculate primary melt compositionsin equilibrium with the most magnesian Macquarie Island olivines(Fo90·5). Fractionated, Group II, basaltic glasses aresaturated with olivine + plagioclase ± clinopyroxene,and have lower mg-number (57–67), and relatively low Al2O3and CaO contents. Group I glasses define a seriate variationwithin the compositional spectrum of MORB, and extend the compositionalrange from N-MORB compositions to enriched compositions thatrepresent a new primitive enriched MORB end-member. Comparedwith N-MORB, this new end-member is characterized by relativelylow contents of MgO, FeO, SiO2 and CaO, coupled with high contentsof Al2O3, TiO2, Na2O, P2O5, K2O and incompatible trace elements,and has the most radiogenic Sr and Pb regional isotope composition.These unusual melt compositions could have been generated bylow-degree partial melting of an enriched mantle peridotitesource, and were erupted without significant mixing with commonN-MORB magmas. The mantle in the Macquarie Island region musthave been enriched and heterogeneous on a very fine scale. Wesuggest that the mantle enrichment implicated in this studyis more likely to be a regional signature that is shared bythe Balleny Islands magmatism than directly related to the hypotheticalBalleny plume itself. KEY WORDS: mid-ocean ridge basalts; Macquarie Island; glass; petrology; geochemistry  相似文献   

13.
Fe–Mg exchange is the most important solid solution involvedin partial melting of spinel lherzolite, and the system CaO–MgO–Al2O3–SiO2–FeO(CMASF) is ideally suited to explore this type of exchange duringmantle melting. Also, if primary mid-ocean ridge basalts arelargely generated in the spinel lherzolite stability field bynear-fractional fusion, then Na and other highly incompatibleelements will early on become depleted in the source, and themelting behaviour of mantle lherzolite should resemble the meltingbehaviour of simplified lherzolite in the CMASF system. We havedetermined the isobarically univariant melting relations ofthe lherzolite phase assemblage in the CMASF system in the 0·7–2·8GPa pressure range. Isobarically, for every 1 wt % increasein the FeO content of the melt in equilibrium with the lherzolitephase assemblage, the equilibrium temperature is lower by about3–5°C. Relative to the solidus of model lherzolitein the CaO–MgO–Al2O3–SiO2 system, melt compositionsin the CMASF system are displaced slightly towards the alkalicside of the basalt tetrahedron. The transition on the solidusfrom spinel to plagioclase lherzolite has a positive Clapeyronslope with the spinel lherzolite assemblage on the high-temperatureside, and has an almost identical position in P–T spaceto the comparable transition in the CaO–MgO–Al2O3–SiO2–Na2O(CMASN) system. When the compositions of all phases are describedmathematically and used to model the generation of primary basalts,temperature and melt composition changes are small as percentmelting increases. More specifically, 10% melting takes placeover 1·5–2°C, melt compositions are relativelyinsensitive to the degree of melting and bulk composition, andequilibrium and near-fractional melting yield similar melt compositions.FeO and MgO are the oxides that exhibit the greatest changein the melt with degree of melting and bulk composition. Theamount of FeO decreases with increasing degree of melting, whereasthe amount of MgO increases. The coefficients for Fe–Mgexchange between the coexisting crystalline phases and melt,KdFe–Mgxl–liq, show a relatively simple and predictablebehaviour with pressure and temperature: the coefficients forolivine and spinel do not show significant dependence on temperature,whereas the coefficients for orthopyroxene and clinopyroxeneincrease with pressure and temperature. When melting of lherzoliteis modeled in the CMASF system, a strong linear correlationis observed between the mg-number of the lherzolite and themg-number of the near-solidus melts. Comparison with meltingin the CMASN system indicates that Na2O has a strong effecton lherzolite melting behaviour only at small degrees of melting. KEY WORDS: CMASF; lherzolite solidus; mantle melting  相似文献   

14.
Ultra-calcic ankaramitic magmas or melt inclusions are ubiquitousin arc, ocean-island and mid-ocean ridge settings. They areprimitive in character (XMg > 0·65) and have highCaO contents (>14 wt %) and CaO/Al2O3 (>1·1). Experimentson an ankaramite from Epi, Vanuatu arc, demonstrate that itsliquidus surface has only clinopyroxene at pressures of 15 and20 kbar, with XCO2 in the volatile component from 0 to 0·86.The parental Epi ankaramite is thus not an unfractionated magma.However, forcing the ankaramite experimentally into saturationwith olivine, orthopyroxene and spinel results in more magnesian,ultra-calcic melts with CaO/Al2O3 of 1·21–1·58.The experimental melts are not extremely Ca-rich but high inCaO/Al2O3 and in MgO (up to 18.5 wt %), and would evolve tohigh-CaO melts through olivine fractionation. Fractionationmodels show that the Epi parent magma can be derived from suchultra-calcic experimental melts through mainly olivine fractionation.We show that the experimental ultra-calcic melts could formthrough low-degree melting of somewhat refractory mantle. Thelatter would have been depleted by previous melt extraction,which increases the CaO/Al2O3 in the residue as long as someclinopyroxene remains residual. This finding corrects the commonassumption that ultra-calcic magmas must come from a Ca-richpyroxenite-type source. The temperatures necessary for the generationof ultra-calcic magmas are  相似文献   

15.
The Ueno Basalts of central Japan comprise a monogenetic volcaniccone complex that was active between 2·76 and 1·34Ma. Basalts were erupted at more than 14 centers scattered overa region 40 km in diameter. Alkali basalt was erupted first,followed by sub-alkaline basalt. Quasi-concentric expansionof eruption centers coinciding with uplift and with decreasingalkalinity of the lavas suggests that Ueno magmatism originatedfrom a mantle diapir as it mushroomed at the base of the lithosphere.Depleted asthenospheric mantle (alkali basalt), enriched lithosphericmantle (sub-alkaline basalt), and crustal components are identifiedas chemical end-members in the petrogenesis of the Ueno Basalts.Incompatible trace element abundances indicate that the Uenoalkali basalts are typical within-plate basalts, whereas thesub-alkaline basalts show strong affinities with normal arclavas. Sr–Nd–Pb isotopic compositions indicate thatthe mantle source of the alkali basalts was more depleted thanthat of the sub-alkaline basalts. About 7% melting of asthenosphericmantle in the garnet-lherzolite stability field produced theprimitive alkali basalts and 12% melting of spinel lherzolitewithin the subcontinental lithosphere produced the primitivesub-alkaline basalts. Isotopic compositions and fluid mobile/immobileelement ratios broadly covary with SiO2 contents in the sub-alkalinesuite, and increasing silica content is associated with strongerEMII (Enriched Mantle II) isotope affinities and fluid mobileelement abundances. A progressive AFC (assimilation–fractionalcrystallization) model assuming assimilation of a low-K silicicmelt reproduces the chemical variations observed in the sub-alkalinesuite. Melting of a flattening mantle diapir at the base ofthe lithosphere is the dominant cause of Ueno magmatism, accompaniedby the assimilation of older arc crust. KEY WORDS: arc basalt; crustal assimilation; mantle heterogeneity; Ueno Basalts  相似文献   

16.
Major and trace element and Sr–Nd–Pb isotopic variationsin mafic volcanic rocks hve been studied in a 220 km transectacross the Kamchatka arc from the Eastern Volcanic Front, overthe Central Kamchatka Depression to the Sredinny Ridge in theback-arc. Thirteen volcanoes and lava fields, from 110 to 400km above the subducted slab, were sampled. This allows us tocharacterize spatial variations and the relative amount andcomposition of the slab fluid involved in magma genesis. TypicalKamchatka arc basalts, normalized for fractionation to 6% MgO,display a strong increase in large ion lithophile, light rareearth and high field strength elements from the arc front tothe back-arc. Ba/Zr and Ce/Pb ratios, however, are nearly constantacross the arc, which suggests a similar fluid input for Baand Pb. La/Yb and Nb/Zr increase from the arc front to the back-arc.Rocks from the Central Kamchatka Depression range in 87Sr/86Srfrom 0·70334 to 0·70366, but have almost constantNd isotopic compositions (143Nd/144Nd 0·51307–0·51312).This correlates with the highest U/Th ratios in these rocks.Pb-isotopic ratios are mid-ocean ridge basalt (MORB)-like butdecrease slightly from the volcanic front to the back-arc. Theinitial mantle source ranged from N-MORB-like in the volcanicfront and Central Kamchatka Depression to more enriched in theback-arc. This enriched component is similar to an ocean-islandbasalt (OIB) source. Variations in (CaO)6·0–(Na2O)6·0show that degree of melting decreases from the arc front tothe Central Kamchatka Depression and remains constant from thereto the Sredinny Ridge. Calculated fluid compositions have asimilar trace element pattern across the arc, although minordifferences are implied. A model is presented that quantifiesthe various mantle components (variably depleted N-MORB-mantleand enriched OIB-mantle) and the fluid compositions added tothis mantle wedge. The amount of fluid added ranges from 0·7to 2·1%. The degree of melting changes from  相似文献   

17.
New H2O, CO2 and S concentration data for basaltic glasses fromLoihi seamount, Hawaii, allow us to model degassing, assimilation,and the distribution of major volatiles within and around theHawaiian plume. Degassing and assimilation have affected CO2and Cl but not H2O concentrations in most Loihi glasses. Waterconcentrations relative to similarly incompatible elements inHawaiian submarine magmas are depleted (Loihi), equivalent (Kilauea,North Arch, Kauai–Oahu), or enriched (South Arch). H2O/Ceratios are uncorrelated with major element composition or extentor depth of melting, but are related to position relative tothe Hawaiian plume and mantle source region composition, consistentwith a zoned plume model. In front of the plume core, overlyingmantle is metasomatized by hydrous partial melts derived fromthe Hawaiian plume. Downstream from the plume core, lavas tapa depleted source region with H2O/Ce similar to enriched Pacificmid-ocean ridge basalt. Within the plume core, mantle components,thought to represent subducted oceanic lithosphere, have waterenrichments equivalent to (KEA) or less than (KOO) that of Ce.Lower H2O/Ce in the KOO component may reflect efficient dehydrationof the subducting oceanic crust and sediments during recyclinginto the deep mantle. KEY WORDS: basalt; Hawaii; mantle; plumes; volatiles  相似文献   

18.
Jurassic age volcanic rocks of the Stonyford volcanic complex(SFVC) comprise three distinct petrological groups based ontheir whole-rock geochemistry: (1) oceanic tholeiites; (2) transitionalalkali basalts and glasses; (3) high-Al, low-Ti tholeiites.Major and trace element, and Sr–Nd–Pb isotopic dataindicate that the oceanic tholeiites formed as low-degree partialmelts of normal mid-ocean ridge basalt (N-MORB)-source asthenospheresimilar in isotope composition to the East Pacific Rise today;the alkalic lavas were derived from an enriched source similarto that of E-MORB. The high-Al, low-Ti lavas resemble second-stagemelts of a depleted MORB-source asthenosphere that formed bymelting spinel lherzolite at low pressures. Trace element systematicsof the high-Al, low-Ti basalts show the influence of an enrichedcomponent, which overprints generally depleted trace elementcharacteristics. Tectonic discrimination diagrams show thatthe oceanic tholeiite and alkali suites are similar to present-daybasalts generated at mid-oceanic ridges. The high-Al, low-Tisuite resembles primitive arc basalts with an enriched, alkalibasalt-like overprint. Isotopic data show the influence of recycledcomponents in all three suites. The SFVC was constructed ona substrate of normal Coast Range ophiolite in an extensionalforearc setting. The close juxtaposition of the MORB-like olivinetholeiites with alkali and high-Al, low-Ti basalts suggestsderivation from a hybrid mantle source region that includedMORB-source asthenosphere, enriched oceanic asthenosphere, andthe depleted supra-subduction zone mantle wedge. We proposethat the SFVC formed in response to collision of a mid-oceanridge spreading center with the Coast Range ophiolite subductionzone. Formation of a slab window beneath the forearc duringcollision allowed the influx of ridge-derived magmas or themantle source of these magmas. Continued melting of the previouslydepleted mantle wedge above the now defunct subduction zoneproduced strongly depleted high-Al, low-Ti basalts that werepartially fertilized with enriched, alkali basalt-type meltsand slab-derived fluids. KEY WORDS: CRO; oceanic basalts; California  相似文献   

19.
Olivine + clinopyroxene ± amphibole cumulates have beenwidely documented in island arc settings and may constitutea significant portion of the lowermost arc crust. Because ofthe low melting temperature of amphibole (1100°C), suchcumulates could melt during intrusion of primary mantle magmas.We have experimentally (piston-cylinder, 0·5–1·0GPa, 1200–1350°C, Pt–graphite capsules) investigatedthe melting behaviour of a model amphibole–olivine–clinopyroxenerock, to assess the possible role of such cumulates in islandarc magma genesis. Initial melts are controlled by pargasiticamphibole breakdown, are strongly nepheline-normative and areAl2O3-rich. With increasing melt fraction (T > 1190°Cat 1·0 GPa), the melts become ultra-calcic while remainingstrongly nepheline-normative, and are saturated with olivineand clinopyroxene. The experimental melts have strong compositionalsimilarities to natural nepheline-normative ultra-calcic meltinclusions and lavas exclusively found in arc settings. Theexperimentally derived phase relations show that such naturalmelt compositions originate by melting according to the reactionamphibole + clinopyroxene = melt + olivine in the arc crust.Pargasitic amphibole is the key phase in this process, as itlowers melting temperatures and imposes the nepheline-normativesignature. Ultra-calcic nepheline-normative melt inclusionsare tracers of magma–rock interaction (assimilative recycling)in the arc crust. KEY WORDS: experimental melting; subduction zone; ultra-calcic melts; wehrlite  相似文献   

20.
The origin of potassic lavas with within-plate characteristicsin island are settings is unclear. The volcanic complex of Ringgit—Beser,situated in eastern Java, has erupted lavas of both normal islandare calc-alkaline type and atypical potassic lavas, includingsome highly magnesian lavas. The occurrence of these primitivelavas gives an unusual insight into the source characteristicsof the potassic lavas. The lavas from Ringgit—Beser have a wide range of K2O(1.1–6.4 wt. %) and MgO contents (18.0–1.6 wt.%).The most magnesian lavas have high Ni and Cr contents. The calc-alkalinelavas have incompatible trace element patterns typical of islandare lavas with enrichments in large ion lithophile elements(LILE) and light rare earth elements (LREE) relative to highfield strength elements (HFSE) and heavy REE (HREE). The potassiclavas may be divided into two series on the basis of Ba andNb contents, with the enriched potassic (EK) series having higherBa and Nb contents for a given MgO content than the potassic(K) series. The EK and K series lavas have some incompatibletrace element ratios similar to within-plate lavas (e.g., highCe/Pb, low LILE/HFSE ratios, and low B/Be). However, both theEK series and K series lavas have negative Ti and Zr anomalies,and the EK series lavas have high Ba/La similar to are lavas.There is little distinction in Sr and Nd isotopes between theK and EK series, but the calc-alkaline lavas have lower 87Sr/86Srand higher 143Nd/144Nd ratios than the potassic lavas. The EKseries lavas have lower 206Pb/204Pb and higher 208Pb/204Pb thanthe K series lavas, but similar 207Pb/204Pb ratios. The K serieslavas define an almost horizontal trend in 207Pb–206Pbspace. The Pb isotopic ratios indicate that the EK series lavasare derived from a single mantle source, whereas the K seriesoriginate from a mixture of two mantle components. Calc-alkalinelavas have Pb isotope ratios similar to other calc-alkalineand tholeiitic lavas from Java, and plot on a mixing line betweenIndian Ocean mid-ocean ridge basalt (MORB) and Indian Oceansediment. Incompatible trace element and Pb isotope data for the calc-alkalinelavas indicate that these lavas have a similar source to othercalc-alkaline lavas erupted in Java, namely melts of the IndianOcean MORB mantle fluxed by fluids from the subducted slab.The potassic lavas originate from enriched mantle sources withinthe wedge which have not been affected by recent subductionprocesses. The EK series lavas are derived from a metasomatizedzone which has EMI-type characteristics. The K series lavasare derived from mixing of melts from Christmas Island-type(EMII) mantle and the metasomatized zone. The metasomatizedzone is probably situated at the base of the lithosphere andthe Indian Ocean MORB and Christmas Island-type mantle componentsare situated in the asthenosphere of the wedge. Isotopic datafor Ringgit—Beser lavas confirm that the mantle wedgeof the Sunda arc is extremely heterogeneous (Foden & Varne,1980; Varne, 1985; Wheller et al., 1987). The similarity in geochemistry between Indonesian potassic lavasand those erupted in continental settings indicates that themagma source is essentially the same, namely a metasomatizedphlogopite-rich layer generated by melts of recycled subductedlithosphere. The lack of negative Ti anomalies in the continentalpotassic lavas is ascribed to lower oxidation states in themantle in continental settings.  相似文献   

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