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1.
Palaeogene basalts from the margins of the North Atlantic oftenshow geochemical variations that are consistent with their parentalmagmas having interacted with the lithosphere en route to theEarth’s surface. These geochemical trends vary dependingon the nature of the local lithospheric contaminants. Usingexamples from the British Tertiary Igneous Province and SE Greenland,we construct coherent contamination trends, which converge ona restricted Pb isotope composition, apparently indicating acommon uncontaminated asthenospheric mantle component. Significantly,this composition is also suitable as one end-member of the Pbisotope arrays recorded in Recent Icelandic basalts. We concludethat this composition has been a persistent component of theIceland plume over 60 my, dominating the mantle contributionto the Palaeocene phase of flood basalt magmatism but constitutingonly one end-member on Iceland. The Pb isotope composition ofthis ‘North Atlantic end-member’ is consistent with,but not necessarily demanding of, a primordial source. Recentevidence suggesting a lower-mantle origin for mantle plumesencourages investigation of whether the geochemical evidencesupports that hypothesis. Helium isotope data from PalaeogeneNorth Atlantic basalts support a lower-mantle contribution.However, mixing models suggest that it is unlikely that thelower-mantle contribution is large enough to dominate the Sr–Nd–Pbisotope compositions and lithophile trace element signaturesof any plume-derived basalts. KEY WORDS: North Atlantic; Iceland; lower mantle; mantle plumes; flood basalts; isotopes  相似文献   

2.
Two apparently distinct, sub-parallel, paleo-subduction zonescan be recognized along the northern margin of the Tibetan Plateau:the North Qilian Suture Zone (oceanic-type) with ophioliticmélanges and high-pressure eclogites and blueschistsin the north, and the North Qaidam Belt (continental-type) inthe south, an ultrahigh-pressure (UHP) metamorphic terrane comprisingpelitic and granitic gneisses, eclogites and garnet peridotites.Eclogites from both belts have protoliths broadly similar tomid-ocean ridge basalts (MORB) or oceanic island basalts (OIB)in composition with overlapping metamorphic ages (480–440Ma, with weighted mean ages of 464 ± 6 Ma for North Qilianand 457 ± 7 Ma for North Qaidam), determined by zirconU–Pb sensitive high-resolution ion microprobe dating.Coesite-bearing zircon grains in pelitic gneisses from the NorthQaidam UHP Belt yield a peak metamorphic age of 423 ±6 Ma, 40 Myr younger than the age of eclogite formation, anda retrograde age of 403 ± 9 Ma. These data, combinedwith regional relationships, allow us to infer that these twoparallel belts may represent an evolutionary sequence from oceanicsubduction to continental collision, and continental underthrusting,to final exhumation. The Qilian–Qaidam Craton was probablya fragment of the Rodinia supercontinent with a passive marginand extended oceanic lithosphere in the north, which was subductedbeneath the North China Craton to depths >100 km at c. 423Ma and exhumed at c. 403 Ma (zircon rim ages in pelitic gneiss). KEY WORDS: HP and UHP rocks; subduction belts; zircon SHRIMP ages; Northern Tibetan Plateau  相似文献   

3.
Site 1201D of Ocean Drilling Program Leg 195 recovered basalticand volcaniclastic units from the West Philippine Basin thatdocument the earliest history of the Izu–Bonin–Marianaconvergent margin. The stratigraphic section recovered at Site1201D includes 90 m of pillow basalts, representing the WestPhilippine Basin basement, overlain by 459 m of volcaniclasticturbidites that formed from detritus shed from the Eocene–Oligoceneproto-Izu–Bonin–Mariana island arc. Basement basaltsare normal mid-ocean ridge basalt (N-MORB), based on their abundancesof immobile trace elements, although fluid-mobile elements areenriched, similar to back-arc basin basalts (BABB). Sr, Nd,Pb and Hf isotopic compositions of the basement basalts aresimilar to those of basalts from other West Philippine Basinlocations, and show an overall Indian Ocean MORB signature,marked by high 208Pb/204Pb for a given 206Pb/204Pb and high176Hf/177Hf for a given 143Nd/144Nd. Trace element and isotopicdifferences between the basement and overlying arc-derived volcaniclasticsare best explained by the addition of subducted sediment orsediment melt, together with hydrous fluids from subducted oceaniccrust, into the mantle source of the arc lavas. In contrastto tectonic models suggesting that a mantle hotspot was a sourceof heat for the early Izu–Bonin–Mariana arc magmatism,the geochemical data do not support an enriched, ocean islandbasalt (OIB)-like source for either the basement basalts orthe arc volcanic section. KEY WORDS: back-arc basalts; Izu–Bonin–Marianas; Philippine Sea; subduction initiation; Ocean Drilling Program Leg 195  相似文献   

4.
The volcanic activity of Mts Bambouto and Oku (Western Highlands)and of the Ngaoundere Plateau, in the continental sector ofthe Cameroon Volcanic Line, Equatorial West Africa, ranges inage from Oligocene to Recent. It is characterized by basanitic,alkali basaltic and transitional basaltic series. Mineral chemistry,major and trace element bulk-rock compositions, and geochemicalmodelling suggest that the magmatic series evolved mainly atlow pressure (2–4 kbar) through fractional crystallizationof clinopyroxene and olivine ± magnetite, at moderatelyhydrated (H2O = 0·5–1 wt %) and QFM (quartz–fayalite–magnetite)to QFM + 1 fO2 conditions. Basalts from Ngaoundere (Mioceneto Quaternary) and from the early activity (31–14 Ma)of the Western Highlands have incompatible trace element andSr–Nd isotopic compositions similar to those of oceanicCameroon Line basalts, pointing to a similar asthenosphericmantle source. By contrast, the late (15–4 Ma) WesternHighlands basanites and alkali basalts have anomalously highconcentrations of Sr, Ba and P, and low concentrations of Zr,which are exclusive features of continental Cameroon basalts.The genesis of these latter magmas is consistent with derivationfrom an incompatible element enriched, amphibole-bearing lithosphericmantle source. Western Highlands basalts show a continuous spectrumfrom high to low Sr–Ba–P compositions, and may resultfrom variable amounts of mixing between melts derived from ananhydrous lherzolite source (asthenospheric component) and meltsfrom an amphibole-bearing peridotite source (lithospheric HSrcomponent). New 40Ar/39Ar ages for Mts Oku and Bambouto basalts,combined with previous 40Ar/39Ar and K/Ar ages of basaltic andsilicic volcanics, and with volcanic stratigraphy, suggest aNE–SW younging of the peak magmatic activity in the WesternHighlands. This SW younging trend, extending from the Oligocenevolcanism in northern Cameroon (e.g. Mt Oku) to the still activeMt Cameroon, suggests that the African plate is moving abovea deep-seated mantle thermal anomaly. However, the age and locationof the Ngaoundere volcanism does not conform to the NE–SWyounging trend, implying that the continental sector of theCameroon Volcanic Line cannot be easily interpreted as the surfaceexpression of a single hotspot system. KEY WORDS: Cameroon Line basalts;40Ar/39Ar geochronology; lithospheric and asthenospheric mantle source; hotspot  相似文献   

5.
The South Auckland Volcanic Field is a Pleistocene (1·59–0·51Ma) basaltic intraplate, monogenetic field situated south ofAuckland City, North Island, New Zealand. Two groups of basaltsare distinguished based on mineralogy and geochemical compositions,but no temporal or spatial patterns exist in the distributionof various lava types forming each group within the field: GroupA basalts are silica-undersaturated transitional to quartz-tholeiiticbasalts with relatively low total alkalis (3·0–4·6wt %), Nb (7–29 ppm), and (La/Yb)N (3·4–7·6);Group B basalts are strongly silica-undersaturated basanitesto nepheline-hawaiites with high total alkalis (3·3–7·9wt %), Nb (32–102 ppm), and (La/Yb)N (12–47). GroupA has slightly higher 87Sr/86Sr, similar Nd, and lower 206Pb/204Pbvalues compared with Group B. Contrasting geochemical trendsand incompatible element ratios (e.g. K/Nb, Zr/Nb, Ce/Pb) areconsistent with separate evolution of Groups A and B from dissimilarparental magmas derived from distinct sub-continental lithosphericmantle sources. Differentiation within each group was controlledby olivine and clinopyroxene fractionation. Group B magmas weregenerated by <8% melting of an ocean island basalt (OIB)-likegarnet peridotite source with high 238U/204Pb mantle (HIMU)and enriched mantle (EMII) characteristics possibly inheritedfrom recycled oceanic crust. Group A magmas were generated by<12% melting of a spinel peridotite source also with HIMUand EMII signatures. This source type may have resulted fromsubduction-related metasomatism of the sub-continental lithospheremodified by a HIMU plume. These events were associated withMesozoic or earlier subduction- and plume-related magmatismwhen New Zealand was at the eastern margin of the Gondwana supercontinent. KEY WORDS: continental intraplate basalts; geochemistry; HIMU, EMII; Sr, Nd, and Pb isotopes; South Auckland; sub-continental lithospheric sources  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.
A convergent margin magma series with characteristic low Nband Ta abundances and enrichments in alkalis and alkaline earthsis intercalated with typical intraplate alkalic basalts in aback-arc setting, 200–250 km above the Wadati-Benioffzone on the North Island, New Zealand. These two contrastingmagma types, together with late-stage K-rich maflc lavas, wereerupted over a short time period (1{dot}60–2{dot}74 Ma)and constitute the Alexandra Volcanics. Field relationshipsindicate that these diverse magma types were contemporaneous,and thus their mantle source regions coexisted, in a singletectonic environment. The convergent margin magma series forms a linear chain of stratovolcanoesaligned at right angles to the present subduction zone. Closed-systempolybaric fractional crystallization models can explain theevolution from ankaramites to transitional olivine basalts toolivine tholeiites to high-Al basalts to medium- and high-Kandesites. The most primitive lavas have geochemical (high LIL/LREEand LIL/HFS element ratios) and Sr, Nd, and Pb isotopic compositionstypical of convergent margin magmas. Calculated source compositionssuggest that three components are involved: a MORB component,a component derived from subducted oceanic crust, and a contributionfrom subducted sediments. The alkalic basalts occur as dispersed monogenetic volcanoesand are intercalated with the larger convergent margin stratovolcanocs.These basalts are enriched in LILE, LREE, Nb, and Ta, and havelow Ba/Nb and Ba/La ratios, all of which are characteristicof ocean island (intraplate) basalts (OIBs). Their relativelyhigh Nd (+5{dot}5 and low 87Sr/86Sr(0{dot}703l–0{dot}7036)are also typical of OIBs. These alkalic magmas were derivedfrom the underlying continental lithospheric mantle that hasbeen enriched by upward-migrating silica-undersaturated melts,probably including volatiles, from the low- velocity zone. Asubducted slab component is not required to account for theirincompatible element enriched character. The K-rich mafic lavas, basanites, and absarokites are volumetricallyminor and cap the largest of the stratovolcanoes, Pirongia.The basanites have geochemical and isotopic compositions whichsuggest they are mixtures of multiple source components, includingthe alkalic and convergent margin region.  相似文献   

8.
Sikhote-Alin and Sakhalin are located in the Russian Far Eastflank of the northernmost part of the Sea of Japan. Magmatismin this region preceded, was concurrent with, and continuedafter the extension and sea-floor spreading (25–18 Ma)that formed the Sea of Japan. Among the Sikhote-Alin and Sakhalinvolcanic suites, Eocene–Oligocene (55–24 Ma) lavasare characterized by greater large ion lithophile element andrare earth element enrichments compared with Early–Mid-Miocene(23–15 Ma) tholeiites, and also show a depletion in highfield strength elements (HFSE). The geochemical characteristicsof the Eocene–Oligocene and Early–Mid-Miocene basaltsare consistent with migration of the locus of magma generationbeneath the Sikhote-Alin and Sakhalin areas from subduction-modifiedlithospheric mantle into mid-ocean ridge basalt (MORB)-sourceasthenosphere as spreading in the Sea of Japan progressed. Mid-Miocene–Pliocene(14–5 Ma) lavas, erupted following the opening of theSea of Japan, include alkaline and sub-alkaline basalts withwide ranges in trace-element abundances, varying between twodistinct end-members: (1) volumetrically minor alkaline basaltswith Zr–Nb and Sr–Nb–Pb isotope compositionssimilar to asthenosphere-derived, intra-plate–hotspotbasalts from eastern China; (2) more abundant, lithosphere-derived,low-alkali tholeiites depleted in HFSE. The similarity of isotopicsignatures coupled with systematically different rare earthelement (REE) abundances in the Mid-Miocene–Pliocene andChinese basalts are best modeled by similar extents of meltingof spinel lherzolite and garnet lherzolite, respectively. TheMid-Miocene–Pliocene alkali basalts were generated bysmall degrees of partial melting of hot asthenosphere beneatha thin lithospheric lid; the thin lithospheric mantle beneaththe Sikhote-Alin and Sakhalin region resulted from heating andextension associated with the opening of the Sea of Japan. KEY WORDS: north-eastern Eurasian margin; Sikhote-Alin–Sakhalin; Japan Sea opening; subcontinental lithosphere; asthenosphere  相似文献   

9.
The Ordovician Snowdon Volcanic Centre (SVC) of North Walescomprises a bimodal basalt–subalkaline/peralkaline associationemplaced around a caldera within a shallow marine environment.The tectonic setting was associated with closure of the LowerPalaeozoic Iapetus Ocean and cessation of ocean plate subduction.The SVC volcanic products include basaltic lavas and pyroclasticrocks, rhyolitic pyroclastic flow deposits, high-level intrusions,domes, and flows, together with reworked equivalents. A programmeof detailed field mapping, sampling, and chemical analysis hasbeen used to evaluate the structure and magmatic evolution ofthe SVC volcanic system. SVC basalts show a range in chemicalcharacteristics between volcanic arc type and within-plate,ocean island basalt (OIB) type. Subalkaline, silica-oversaturatedintermediate intrusions (icelandites) and five chemically distinctgroups of extrusive and intrusive subalkaline/peralkaline rhyolites(termed A1, A2, B1, B2, and B3) were emplaced during the evolutionof the SVC. This evolution was driven by material and thermalinput from basaltic magma. The SVC basaltic lavas were derivedas partial melts from a heterogeneous volcanic arc to OIB-typespinel lherzolite mantle and experienced up to 60% olivine gabbrofractionation during storage in sill networks in the sub-crustor lower crust. Some magma batches experienced further fractionalcrystallization ({small tilde}70%) and minor crustal contamination({small tilde}10%) to yield the icelandites. Trace element andNd isotope data do not favour an origin for the rhyolites bypartial or total fusion of likely crustal material, and thefive rhyolite groups are regarded as distinct homogeneous batchesof magma derived from varied basaltic magmas. The icelanditesand peralkaline rhyolites (group B3) result, respectively, from{small tilde}50% and {small tilde}80–90% zircon-free fractionalcrystallization of SVC basalts. The subalkaline rhyolites (groupsA1 and B1) result from {small tilde}80–90% fractionalcrystallization of subduction-related basalts similar to thoseof Ordovician basalts which pre-date the Lower Rhyolitic TuffFormation, and groups A2 and B2 were formed by mixing and homogenizationof A1, B1, and B3 magma batches. These data and interpretationsprovide the basis of a model for the complex evolution of asilicic magma system below the SVC caldera around the time ofcessation of Caledonian subduction in North Wales. Rhyolitemagma chambers were short lived and discontinuous; the largestwas probably disc shaped and was almost entirely evacuated duringa >60-km3 ash-flow eruption.  相似文献   

10.
Major element variations in North Atlantic Tertiary Provinceprimitive, early erupted, alkaline-transitional-tholeiite basalts,recalculated to a restricted value of MgO, give insights intothe process of plume-related magmatism. Basalts primitive enoughto be crystallizing only olivine were recalculated to a proposedprimary magma composition of 15 wt % MgO. The recalculated datasetshows clear inter-element correlations including a strong, significant,negative correlation between Fe and Si indicating polybaricmelt segregation. Overlap between basalt compositions and experimentalmelts from a fertile, Fe-rich, low mg-number (85.5) peridotitesuggests that, relative to normal peridotite with mg-number> 89, the North Atlantic basalt source was Fe rich. Linearregression of the experimental data gives apparent pressuresof magma segregation of 17·5–37 kbar, with intra-regionvariability in the depth derivation from the melt column foreach sample, thus suggesting that lithospheric thickness ‘lid-effect’control on magma generation may have been overemphasized inrecent studies. Comparable source composition, magma segregationdepth and calculated mantle potential temperature (1440–1460°C)throughout the Province supports the previously suggested plumeimpact model, arriving below East Greenland, derived from avariably enriched and depleted lower-mantle source. Given thegood agreement between conclusions drawn from major elementdata and previously published results we suggest that restricted-MgOrecalculated datasets may be usefully applied to study otherlarge igneous provinces. KEY WORDS: basalt; Fe-rich mantle; large igneous provinces; North Atlantic Tertiary Province; restricted-MgO major element datasets  相似文献   

11.
Kimberlites from Southern Africa, along with their low-Cr megacrysts,have unusual Hf–Nd isotopic characteristics. Group I andTransitional kimberlites define arrays trending oblique to,and well below, the Nd–Hf isotope ‘mantle array’,defined by oceanic basalts, i.e. they have negative  相似文献   

12.
Oxygen isotope ratios determined by laser fluorination analysison olivine, clinopyroxene and plagioclase separated from 31Oligocene flood basalts and rhyolites from Yemen display smallbut significant variations (5·1–6·2  相似文献   

13.
The Paran continental flood basalt province is a voluminousbimodal volcanic sequence, with <5% silicic rocks (‘rhyolites’)lying on top of the basalts, concentrated towards the SouthAtlantic margin. Petrographically, the rhyolites have an anhydrousmineralogy (plagioclase, pyroxene, Fe–Ti oxides), and.two distinct groups are defined on the basis of phenocryst abundance.The Palmas group rhyolites are almost aphyric (<5% phenocrysts),in contrast to the plagioclase-rith Chapec group rhyolites(<25% phenocrysts). The plagioclase and clinopyroxene phenocrystsin the Palmas group rhyolites are rounded and poorly preserved,and are compositionally less evolved than those in the Chapecgroup. Calculated eruption temperatures are unusually high forsilicic magmas (950–1100C), and lie within the rangeof temperatures for the associated flood basalts. Chemically,the Palmas and Chapec group rhyolites are clearly distinguishable,with the most striking feature being the higher high field strengthelements, notably Ti, in the Chapec group. This mirrors thewell-documented low- and high-Ti division of the Paran basalts,and in addition there is a geographic correlation between thelow- and high- Ti basalt and rhyolite provinces, with high-Tivolcanics predominating in the north of the Paran Basin, andlow-Ti in the south. The Chapec group have Sr and Nd isotoperatios which overlap with those of the high-Ti basalts (87Sr/86Sr1300•705–0•708), whereas the Palmas group exhibita range towards high Sr isotope ratios (87Sr/86Sr130 0•714–0•727),continuing the trend of the low-Ti basalts to more radiogenicvalues. This suggests that assimilation of radiogenic materialhas occurred. Both rhyolite groups plot away from the isotopicfields for crustal basement types beneath the Paran, thus anorigin by simple crustal melting is discounted. Based on petrographic,chemical and isotopic data, petrogenetic models for the tworhyolite groups are developed, focusing on the clear geneticlink between the Palmas rhyolites and the low-Ti basalts, andthe Chapec rhyolites and the high-Ti basalts. The Chapec rhyolitesare modelled as partial melts ( 30%) of underplated high-Tibasalts, rather than fractionates, primarily because of thetime gap between eruption of the high-Ti basalts and Chapecrhyolites. However, the Palmas rhyolites are almost coeval withthe low-Ti basalts, and are modelled as the products of open-systemfractional crystallization from these low-Ti basaltic magmas.In addition, this low-Ti suite shows a continuous trend frombasalt to rhyolite in highly incompatible elements such as Zrand Hf consistent with a liquid line of descent, whereas thehigh-Ti magmas have a substantial gap in the concentration ofthese elements between the basalts and rhyolites. Experimentaldata support the derivation of both Paran rhyolite groups frombasaltic parents with moderately low water contents. Pressurecalculations suggest shallower ponding for the Palmas magmasthan for the Chapec magma (<5 kbar vs 5–15 kbar),and the style of eruption inferred for the two groups is explosive(rheoignimbritic) for the Palmas group, and effusive (lava flows)for the Chapec group. KEY WORDS: Paran; Brazil; rhyolits; petrogenesis; geochemistry *Corresponding author  相似文献   

14.
Hawaiian volcanoes, dominantly shields of tholeiitic basalt,form as the Pacific Plate migrates over a hotspot in the mantle.As these shields migrate away from the hotspot, highly alkaliclavas, forming the rejuvenated stage of volcanism, may eruptafter an interval of erosion lasting for 0·25–2·5Myr. Alkalic lavas with geochemical characteristics similarto rejuvenated- stage lavas erupted on the sea floor north ofOahu along the Hawaiian Arch. The variable Tb/Yb, Sr/Ce, K/Ce,Rb/La, Ba/La, Ti/Eu and Zr/Sm ratios in lavas forming the NorthArch and the rejuvenated-stage Honolulu Volcanics were controlledduring partial melting by residual garnet, clinopyroxene, Fe–Tioxides and phlogopite. However, the distinctively high Ba/Thand Sr/Nd ratios of lava forming the North Arch and HonoluluVolcanics reflect source characteristics. These characteristicsare also associated with shield tholeiitic basalt; hence theyarise from the Hawaiian hotspot, which is interpreted to bea mantle plume. Inversion of the batch melting equation usingabundances of highly incompatible elements, such as Th and La,requires enriched sources with 10–55% clinopyroxene and5–25% garnet for North Arch lavas. The 87Sr/86Sr and 143Nd/144Ndratios in lavas forming the North Arch and Honolulu Volcanicsare consistent with mixing between the Hawaiian plume and adepleted component related to mid-ocean ridge basalts. Specifically,the enrichment of incompatible elements coupled with low 87Sr/86Srand high 143Nd/144Nd relative to bulk Earth ratios is best explainedby derivation from depleted lithosphere recently metasomatizedby incipient melt (<2% melting) from the Hawaiian plume.In this metasomatized source, the incompatible element abundances,as well as Sr and Nd isotopic ratios, are controlled by incipientmelts. In contrast, the large range of published 187Os/188Osdata (0·134–0·176) reflects heterogeneitycaused by various proportions of pyroxenite veins residing ina depleted peridotite matrix. KEY WORDS: Hawaiian plume; Honolulu Volcanics; North Arch; plume–lithosphere interaction; rejuvenated stage; trace element geochemistry; alkalic lavas  相似文献   

15.
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   

16.
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   

17.
Continental flood basalts from the Parana plateau are of LowerCretaceous age and are represented by abundant (c. 45 per centby volume) two-pyroxene tholeiites characterized by relativelylow-TiO2 (< 2 wt. percent) and incompatible (e.g., P, Ba,Sr, La, Ce, Zr) element contents. Low-Ti basalts are distributedthroughout the Parana Basin and predominate in the southernregions, where they represent over 90 per cent by volume ofthe basic activity. Major and trace elements and Sr-Nd isotope ratios were analysedin 43 low-Ti basalts selected so as to cover the entire Paranabasin. In general, low-Ti basalts with initial 87Sr86Sr ratios (R0)lower than O7060 may be divided into two groups: (A) those relativelyenriched in incompatible elements (e.g., average K2O = O.85and P2O5 = 0.27 wt. per cent, and Ba = 346, Sr =289, Rb=16;La =18; Zr=132 p.p.m.) and SiO2 (average 51.1 wt. per cent);and (B) depleted in incompatible elements (e.g., average K2O= 0.31, P2O5 =0.17 wt. per cent, and Ba=178, Sr= 179, Rb= 11,La = 9, Zr = 93 p.p.m.) and SiO2 (average 49.7 wt. per cent).Low-Ti basalts of Group A are typical of northern Paran? {Ro= O70550–O70596), but a few are also present in centralParan? (Ro = 070577–0–70591), while those of GroupB are exclusive to central Paran– {Ro = 070463–0–70580) Low-Ti basalts with R0> O7060 are typical of southern Paran?(R0 = O7O639 –O71137), but are also present in centralParana (Ro = 070620–070890). These low-Ti basalts havechemical similarity (e.g., Ti, P, Sr) with low-Ti basalts depletedin incompatible elements (Group B) from which, however, theydiffer-in possessing significantly higher concentrations ofSiO2, K2O, Rb, and Ba. Such chemical diversity, accompaniedby important Ro variations (070463–071137) suggests thatthe low-Ti basalts from southern and part of central Paranamay result from crustal contamination. On the contrary, low-Ti basalts from northern, and part of central, Parana (GroupA) may be considered virtually uncontaminated. Results indicate that crustal contamination by granitic material(s)may be in the range 7–17 per cent. Such contaminationin central Paran? appears compatible with an assimilation-fractionalcrystallization process (AFC), while in southern Parana, othercontamination processes (e.g., mixing of magmasfrom crustaland mantle sources, assimilation of wall rock while magmas flowthrough dykes, etc.) were probably superimposed on AFC. Thedegree of crustal contamination generally decreases from southernto northern Parana. Sr and Nd isotope ratios suggest that mantle source materialfor low-Ti basalts depleted in incompatible elements (GroupB: southern and part of central Parana) had a lower R0 value(c. O.7046) and a higher l43Nd/144Nd ratio (Nd + c. 0.51274)than that for low-Ti basalts enriched in incompatible elements(Group A: northern and part of central Parana), namely R0 c.O.7059 and Nd+ c. 0.51242. These Sr-isotopic differences alsoapply to the northern (incompatible-element rich, R0 c. O.7053)and southern (incompatible-element poor R0 c. 0.7046) basaltprovinces of Karoo, suggesting that both Parana and Karoo basaltmagmas, differing by about 70 m.y. in age, probably originatedin a similar batch of subcontinental lithospheric mantle inpredrift times (cf. Cox, 1986). The extension of the Dupal Sr-anomaly (i.e. Rio Grande Rise+ Wai vis Ridge + Gough and Tristan da Cunha islands: Sr = 46=53;Hart, 1984) inside the Brazilian continent (Sr = 46–59)suggests that the lithospheric mantle of the Parana (and Karoo)provinces was possibly also the local source of oceanic volcanismup to advanced stages of the opening of the South Atlantic. *Reprint requests to E. M. Piccirillo.  相似文献   

18.
Island arc volcanism in the Greater Antilles persisted for >70m.y. from Middle Cretaceous to Late Eocene time. During theinitial 50 m.y., lavas in central Puerto Rico shifted from predominantlyisland arc tholeiites (volcanic phase I, Aptian to Early Albian,120–105 Ma), to calc-alkaline basalts (phase II, LateAlbian, 105–97 Ma), and finally to high-K, incompatible-element-enrichedbasalts (phases III and IV, Cenomanian–Maastrichtian,97–70 Ma). Following an island-wide eruptive hiatus, geochemicaltrends were reversed in the Eocene with renewed eruption ofcalc-alkaline basalts (phase V, 60–45 Ma). Progressiveincreases in large-ion lithophile elements (LILE)/light rareearth elements (LREE), LILE/high field strength elements (HFSE),LREE/HFSE, and HFSE/heavy rare earth elements (HREE) characterizethe compositional evolution of the first four volcanic phases.The shift in trace element compositions is mirrored by increasingradiogenic content of the lavas. Pb  相似文献   

19.
The Pliocene—Pleistocene magmatic activity of the Zamboangaare is linked to the southward subduction of the Oligocene—Mio-ceneSulu Sea back-are basin along the Sulu Trench. The magmaticproducts include small amounts of adakites dated from 3.8 to0.7 Ma, abundant Nb-enriched basalts and basaltic andesites(NEB) dated from 2 to 1 Ma and a lone calc-alkaline potassicbasaltic andesite dated at 0.4 Ma. Three kinds of NEB are distinguished:nearly primitive Mg-rich (MG) basalts displaying positive orno Nb anomalies with respect to adjacent incompatible elementsand more evolved low-K (LK) and calc-alkaline (CA) lavas which,despite their Nb enrichment, display negative Nb anomalies.Although the role of OIB-type mantle components has been advocatedto explain the HFSE enrichment of NEB, the spatial and temporalassociation of these rocks with adakites suggests a petrogeneticlink between them. Trace element characteristics of the NEBimply that amphibole and ilmenite might be present in theirsource. We suggest that these minerals could be added metasomaticallyto the mantle through hybridization by percolating slab melts,during which Nb and Ti are preferentially extracted from theadakitic melts. In an early stage (4–3 Ma) of the subductionof the young and hot Sulu Sea basin crust beneath the Zamboangapeninsula, adakitic liquids formed at depths of 75–85km. A few of them were emplaced at the surface but most wereconsumed through slab melt-mantle metasomatic reactions. Adakiteproduction and emplacement continued later (<2 Ma), whilethe Nb-enriched mantle was brought by convection to depths thatallowed its melting and the subsequent emplacement of NEB behindthe adakitic front of the Zamboanga are. KEY WORDS: adakite; metasomatism; Mindanao; Nb-enriched basalts; subduction *Corresponding author. Present address: Mines and Geosciences Bureau, North Avenue, Diliman, 1100 Quezon City, Philippines  相似文献   

20.
We report major and trace element X-ray fluorescence (XRF) datafor mafic volcanics covering the 15-Ma evolution of Gran Canaria,Canary Islands. The Miocene (12–15 Ma) and Pliocene-Quaternary(0–6 Ma) mafic volcanics on Gran Canaria include picrites,tholeiites, alkali basalts, basanites, nephelinites, and melilitenephelinites. Olivineclinopyroxene are the major fractionatingor accumulating phases in the basalts. Plagioclase, Fe–Tioxide, and apatite fractionation or accumulation may play aminor role in the derivation of the most evolved mafic volcanics.The crystallization of clinopyroxene after olivine and the absenceof phenocrystic plagioclase in the Miocene tholeiites and inthe Pliocene and Quaternary alkali basalts and basanites withMgO>6 suggests that fractionation occurred at moderate pressure,probably within the upper mantle. The presence of plagioclasephenocrysts and chemical evidence for plagioclase fractionationin the Miocene basalts with MgO<6 and in the Pliocene tholeiitesis consistent with cooling and fractionation at shallow depth,probably during storage in lower-crustal reservoirs. Magma generationat pressures in excess of 3•0–3•5 GPa is suggestedby (a) the inferred presence of residual garnet and phlogopiteand (b) comparison of FeO1 cation mole percentages and the CIPWnormative compositions of the mafic volcanics with results fromhigh-pressure melting experiments. The Gran Canaria mafic magmaswere probably formed by decompression melting in an upwellingcolumn of asthenospheric material, which encountered a mechanicalboundary layer at {small tilde}100-km depth.  相似文献   

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