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1.
The Baikal Rift is a zone of active lithospheric extension adjacentto the Siberian Craton. The 6–16 Myr old Vitim VolcanicField (VVF) lies approximately 200 km east of the rift axisand consists of 5000 km3 of melanephelinites, basanites, alkaliand tholeiitic basalts, and minor nephelinites. In the volcanicpile, 142 drill core samples were used to study temporal andspatial variations. Variations in major element abundances (e.g.MgO = 3·3–14·6 wt %) reflect polybaric fractionalcrystallization of olivine, clinopyroxene and plagioclase. 87Sr/86Sri(0·7039–0·7049), 143Nd/144Ndi (0·5127–0·5129)and 176Hf/177Hfi (0·2829–0·2830) ratiosare similar to those for ocean island basalts and suggest thatthe magmas have not assimilated significant amounts of continentalcrust. Variable degrees of partial melting appear to be responsiblefor differences in Na2O, P2O5, K2O and incompatible trace elementabundances in the most primitive (high-MgO) magmas. Fractionatedheavy rare earth element (HREE) ratios (e.g. [Gd/Lu]n > 2·5)indicate that the parental magmas of the Vitim lavas were predominantlygenerated within the garnet stability field. Forward major elementand REE inversion models suggest that the tholeiitic and alkalibasalts were generated by decompression melting of a fertileperidotite source within the convecting mantle beneath Vitim.Ba/Sr ratios and negative K anomalies in normalized multi-elementplots suggest that phlogopite was a residual mantle phase duringthe genesis of the nephelinites and basanites. Relatively highlight REE (LREE) abundances in the silica-undersaturated meltsrequire a metasomatically enriched lithospheric mantle source.Results of forward major element modelling suggest that meltingof phlogopite-bearing pyroxenite veins could explain the majorelement composition of these melts. In support of this, pyroxenitexenoliths have been found in the VVF. High Cenozoic mantle potentialtemperatures (1450°C) predicted from geochemical modellingsuggest the presence of a mantle plume beneath the Baikal RiftZone. KEY WORDS: Baikal Rift; mafic magmatism; mantle plume; metasomatism; partial melting  相似文献   

2.
Major and trace element, Sr–Nd–Pb isotope and mineralchemical data are presented for newly discovered ultrapotassiclavas in the Tangra Yumco–Xuruco graben in southern Tibet.The ultrapotassic lavas are characterized by high MgO, K2O andTiO2, low Al2O3 and Na2O contents, and also have high molarK2O/Al2O3, molar (K2O + Na2O)/Al2O3 and K2O/Na2O ratios. Theirhigh abundances of incompatible trace elements such as largeion lithophile elements (LILE) and light rare earth elements(LREE) reach the extreme levels typical of lamproites. The lamproitesshow highly radiogenic 87Sr/86Sr (0· 7166–0·7363) and unradiogenic 143Nd/144Nd (0· 511796–0·511962), low 206Pb/204Pb (18· 459–18· 931),and elevated radiogenic 207Pb/204Pb (15· 6732–15·841) and 208Pb/204Pb (39· 557–40· 058) ratios.On the basis of their geochemical and isotopic systematics,the lamproites in south Tibet have a distinct magma source thatcan be differentiated from the sources of potassic lavas inthe east Lhasa and Qiangtang blocks. Their high Nb/Ta ratios(17· 10–19· 84), extremely high Th/U ratios(5· 70–13· 74) and distinctive isotope compositionsare compatible with a veined mantle source consisting of partialmelts of subducted Tethyan oceanic sediments and sub-continentallithospheric depleted mantle. Identification of the lamproitesand the delineation of their mantle source provide new evidencerelevant for models of the uplift and extension of the Tibetanplateau following the Indo-Asia collision. Metasomatism by partialmelts from isotopically evolved, old sediment subducted on theyoung Tethyan slab is an alternative explanation for PrecambrianNd and Pb model ages. In this model, differences in isotopiccomposition along-strike are attributed to differences in thetype of sediment being subducted, thus obviating the need formultiple metasomatic events over hundreds of million years.The distribution of lamproites, restricted within a north–south-trendinggraben, indicates that the initiation of east–west extensionin south Tibet started at 25 Ma. KEY WORDS: lamproites; subducted oceanic sediment; Tibetan active continental collision belt  相似文献   

3.
We present the results of a comprehensive major element, traceelement and Sr–Nd–Pb–O isotopic study of post-glacialvolcanic rocks from the Neovolcanic zones on Iceland. The rocksstudied range in composition from picrites and tholeiites, whichdominate in the main rift systems, to transitional and alkalicbasalts confined to the off-rift and propagating rift systems.There are good correlations of rock types with geochemical enrichmentparameters, such as La/Sm and La/Yb ratios, and with long-termradiogenic tracers, such as Sr–Nd–Pb isotope ratios,indicating a long-lived enrichment/depletion history of thesource region. 87Sr/86Sr vs 143Nd/144Nd defines a negative array.Pb isotopes define well-correlated positive arrays on both 206Pb/204Pbvs 207Pb/204Pb and 208Pb/204Pb diagrams, indicating mixing ofat least two major components: an enriched component representedby the alkali basalts and a depleted component represented bythe picrites. In combined Sr–Nd–Pb isotopic spacethe individual rift systems define coherent mixing arrays withslightly different compositions. The enriched component hasradiogenic Pb (206Pb/204Pb > 19·3) and very similargeochemistry to HIMU-type ocean island basalts (OIB). We ascribethis endmember to recycling of hydrothermally altered upperbasaltic oceanic crust. The depleted component that is sampledby the picrites has unradiogenic Pb (206Pb/204Pb < 17·8),but geochemical signatures distinct from that of normal mid-oceanridge basalt (N-MORB). Highly depleted tholeiites and picriteshave positive anomalies in mantle-normalized trace element diagramsfor Ba, Sr, and Eu (and in some cases also for K, Ti and P),negative anomalies for Hf and Zr, and low 18Oolivine values(4·6–5·0) below the normal mantle range.All of these features are internally correlated, and we, therefore,interpret them to reflect source characteristics and attributethem to recycled lower gabbroic oceanic crust. Regional compositionaldifferences exist for the depleted component. In SW Icelandit has distinctly higher Nb/U (68) and more radiogenic 206Pb/204Pbratios (18·28–18·88) compared with the NErift (Nb/U 47; 206Pb/204Pb = 18·07–18·47).These geochemical differences suggest that different packagesof recycled oceanic lithosphere exist beneath each rift. A thirdand minor component with relatively high 87Sr/86Sr and 207Pb/204Pbis found in a single volcano in SE Iceland (Öræfajökullvolcano), indicating the involvement of recycled sediments inthe source locally. The three plume components form an integralpart of ancient recycled oceanic lithosphere. The slope in theuranogenic Pb diagram indicates a recycling age of about 1·5Ga with time-integrated Th/U ratios of 3·01. Surprisingly,there is little evidence for the involvement of North AtlanticN-MORB source mantle, as would be expected from the interactionof the Iceland plume and the surrounding asthenosphere in formof plume–ridge interaction. The preferential samplingof the enriched and depleted components in the off-rift andmain rift systems, respectively, can be explained by differencesin the geometry of the melting regions. In the off-rift areas,melting columns are truncated deeper and thus are shorter, whichleads to preferential melting of the enriched component, asthis starts melting deeper than the depleted component. In contrast,melting proceeds to shallower depths beneath the main rifts.The longer melting columns also produce significant amountsof melt from the more refractory (lower crustal/lithospheric)component. KEY WORDS: basalts; trace element and Sr, Nd, Pb, O isotope geochemistry; Iceland plume; isotope ratios; oceanic crustal recycling; partial melting; plume–ridge interaction  相似文献   

4.
Within the Zitácuaro–Valle de Bravo (ZVB) regionof the central Mexican Volcanic Belt (MVB), three lava serieshave erupted during the Quaternary: (1) high-K2O basaltic andesitesand andesites; (2) medium-K2O basaltic andesites, andesitesand dacites; (3) high-TiO2 basalts and basaltic andesites. Thedominant feature of the first two groups is the lack of plagioclaseaccompanying the various ferromagnesian phenocrysts (olivine,orthopyroxene, augite, and hornblende) in all but the dacites.This absence of plagioclase in the phenocryst assemblages ofthe high-K2O and medium-K2O intermediate lavas is significantbecause it indicates high water contents during the stage ofphenocryst equilibration. In contrast, the high-TiO2 group ischaracterized by phenocrysts of plagioclase and olivine. Thespatial distribution of these three lava series is systematic.The southern section of the ZVB transect, 280–330 km fromthe Middle America Trench (MAT), is characterized by high-K2Omelts that are relatively enriched in fluid-mobile elementsand have the highest 87Sr/86Sr ratios. Medium-K2O basaltic andesiteand andesite lavas are present throughout the transect, butthose closest to the MAT are MgO-rich (3·5–9·4wt %) and have phenocryst assemblages indicative of high magmaticwater contents (3·5–6·5 wt % water) andrelatively low temperatures (950–1000°C). In markedcontrast, the northern section of the ZVB transect (380–480km from the MAT) has high-TiO2, high field strength element(HFSE)-enriched magmas that have comparatively dry (< 1·5wt % magmatic water) and hot (1100–1200°C) phenocrystequilibration conditions. The central section of the ZVB transect(330–380 km from the MAT) is a transition zone and producesmoderately light rare earth element (LREE) and large ion lithophileelement (LILE)-enriched, medium-K2O lavas with phenocryst assemblagesindicative of intermediate (1·5–3·5 wt %)water contents and temperatures. The high-K2O series compositionsare the most enriched in LILE and LREE, with a narrow rangeof radiogenic 87Sr/86Sr from 0·704245 to 0·704507,143Nd/144Nd values ranging from 0·512857 to 0·512927(Nd = 4·27–5·63), and 208Pb/204Pb valuesfrom 38·248 to 38·442, 207Pb/204Pb values from15·563 to 15·585, and 206Pb/204Pb values from18·598 to 18·688. The medium-K2O series compositionsare only moderately enriched in the LILE and LREE, with a broaderrange of 87Sr/86Sr, but similar 143Nd/144Nd and 208Pb/204Pbvalues to those of the high-K2O series. In contrast, the high-TiO2series compositions have little enrichment in LILE or LREE andinstead are enriched in the HFSE and heavy rare earth elements(HREE). The high-TiO2 lavas are isotopically distinct in theirlower and narrower range of 143Nd/144Nd. The isotopic variationsare believed to reflect the upper mantle magma source regionsas the low content of phenocrysts in most lavas precludes significantupper crustal assimilation or magma mixing, other than thatrepresented by the presence of quartz xenocrysts (< 2 vol.%) with rhyolitic glass inclusions, which are found in manyof these lavas. The systematic spatial variation in compositionof the three lava series is a reflection of the underlying subduction-modifiedmantle and its evolution. KEY WORDS: central Mexico; geochemistry; isotopes; Quaternary volcanism; hydrous lavas  相似文献   

5.
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   

6.
The effects of source composition and source evolution duringprogressive partial melting on the chemistry of mantle-derivedmid-ocean ridge basalt (MORB) melts were tested using a comprehensivegeochemical and Sr–Nd–Pb isotopic dataset for fresh,magnesian basaltic glasses from the Miocene Macquarie Islandophiolite, SW Pacific. These glasses: (1) exhibit clear parent–daughterrelationships; (2) allow simple reconstruction of primary meltcompositions; (3) show exceptional compositional diversity (e.g.K2O/TiO2 0·09–0·9; La/Yb 1·5–22;206Pb/204Pb 18·70–19·52); (4) preserve changesin major element and isotope compositions, which are correlatedwith the degree of trace element enrichment (e.g. La/Sm). Conventionalmodels for MORB genesis invoke melting of mantle that is heterogeneouson a small scale, followed by binary mixing of variably lithophileelement-enriched melt batches. This type of model fails to explainthe compositions of the Macquarie Island glasses, principallybecause incompatible element ratios (e.g. Nb/U, Sr/Nd) and Pbisotope ratios vary non-systematically with the degree of enrichment.We propose that individual melt batches are produced from instantaneous‘parental’ mantle parageneses, which change continuouslyas melting and melt extraction proceeds. This concept of a ‘dynamicsource’ combines the models of small-scale mantle heterogeneitiesand fractional melting. A dynamic source is an assemblage oflocally equilibrated mantle solids and a related melt fraction.Common MORB magmas that integrate the characteristics of numerousmelt batches therefore tend to conceal the chemical and isotopicidentity of a dynamic source. This study shows that isotoperatios of poorly mixed MORB melts are a complex function ofthe dynamic source evolution, and that the range in isotoperatios within a single MORB suite does not necessarily requiremixing of diverse components. KEY WORDS: mid-ocean ridge basalt; Macquarie Island; radiogenic isotopes; mantle; geochemistry  相似文献   

7.
Vico volcano has erupted potassic and ultrapotassic magmas,ranging from silica-saturated to silica-undersaturated types,in three distinct volcanic periods over the past 0·5Myr. During Period I magma compositions changed from latiteto trachyte and rhyolite, with minor phono-tephrite; duringPeriods II and III the erupted magmas were primarly phono-tephriteto tephri-phonolite and phonolite; however, magmatic episodesinvolving leucite-free eruptives with latitic, trachytic andolivine latitic compositions also occurred. In Period II, leucite-bearingmagmas (87Sr/86Srinitial = 0·71037–0·71115)were derived from a primitive tephrite parental magma. Modellingof phonolites with different modal plagioclase and Sr contentsindicates that low-Sr phonolitic lavas differentiated from tephri-phonoliteby fractional crystallization of 7% olivine + 27% clinopyroxene+ 54% plagioclase + 10% Fe–Ti oxides + 4% apatite at lowpressure, whereas high-Sr phonolitic lavas were generated byfractional crystallization at higher pressure. More differentiatedphonolites were generated from the parental magma of the high-Srphonolitic tephra by fractional crystallization of 10–29%clinopyroxene + 12–15% plagioclase + 44–67% sanidine+ 2–4% phlogopite + 1–3% apatite + 7–10% Fe–Tioxides. In contrast, leucite-bearing rocks of Period III (87Sr/86Srinitial= 0·70812–0·70948) were derived from a potassictrachybasalt by assimilation–fractional crystallizationwith 20–40% of solid removed and r = 0·4–0·5(where r is assimilation rate/crystallization rate) at differentpressures. Silica-saturated magmas of Period II (87Sr/86Srinitial= 0·71044–0·71052) appear to have been generatedfrom an olivine latite similar to some of the youngest eruptedproducts. A primitive tephrite, a potassic trachybasalt andan olivine latite are inferred to be the parental magmas atVico. These magmas were generated by partial melting of a veinedlithospheric mantle sources with different vein–peridotite/wall-rockproportions, amount of residual apatite and distinct isolationtimes for the veins. KEY WORDS: isotope and trace element geochemistry; polybaric differentiation; veined mantle; potassic and ultrapotassic rocks; Vico volcano; central Italy  相似文献   

8.
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   

9.
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   

10.
Petrographic and field data indicate the existence of four mainrock types within the allochthonous Cabo Ortegal ultramaficunits: (1) harzburgites; (2) dunites; (3) massive, occasionallygarnet-bearing, pyroxenites; (4) less abundant mafic rocks withvariable amounts of garnet-rich pyroxenite. The major and traceelement compositions of the analysed ultramafic rocks definewell-delimited fields in binary variation diagrams. Normalizedtrace element patterns, however, exhibit large ion lithophileelement (LILE) and light rare earth element (LREE) enrichmentthat do not correlate with the main rock types distinguished.NiO contents and fo-number of olivine in the harzburgites matchthose of the mantle olivine array, whereas a fractional crystallizationtrend is observed from dunites to pyroxenites. Spinel and olivinein the harzburgites have residual characteristics comparablewith those of abyssal peridotites or peridotites from arc settings,whereas in most of the dunites and pyroxenites the range offo-number and Cr/(Cr + Al) ratio suggests crystallization fromprimitive subduction-related magmas. Whole-rock major and traceelement and Pb–Sr–Nd isotope data suggest that regional-scalemassive pyroxenites from Cabo Ortegal originated from relativelyhomogeneous parental melts. Fractional crystallization processes,coeval with intense deformation, might result in the formationof cumulate layers (clinopyroxene, orthopyroxene, olivine, chromite,etc.). Some less abundant mafic rocks and associated pyroxenitesare also homogeneous but have different chemical and isotopicsignatures suggesting a different parental melt from that ofthe massive pyroxenites. Although some differences exist inthe major element and isotopic composition of the clinopyroxenes,their initial isotopic ratios (206Pb/204Pb = 17·845–18·305,207Pb/206Pb = 15·433–15·634; 87Sr/86Sr =0·70330–0·70476; 143Nd/144Nd = 0·512539–0·512916)suggest involvement of an enriched component in their mantlesource, which may be related to the subduction of terrigenoussediments (i.e. EMI). The new data obtained confirm that ultramaficunits of Cabo Ortegal experienced a complex tectonothermal historysimilar to that of other units of the same area and allow usto distinguish at least two different events. Sm–Nd whole-rock–clinopyroxeneages suggest formation of the ultramafic units at  相似文献   

11.
Establishing the petrogenesis of volcanic and plutonic rocksis a key issue in unraveling the evolution of distinct subduction-relatedtectonic phases occurring along the South American margin. Thisis particularly true for Cenozoic times when large volumes ofmagma were produced in the Andean belt. In this study we havefocused on Oligo-Miocene magmatism in central Chile at 33°S.Our data include field and petrographic observations, whole-rockmajor and trace element analyses, U–Pb zircon dating,and Pb, Sr, and Hf isotope analyses of plagioclase, clinopyroxene,and zircon mineral separates. Combined with earlier dating resultsthe new zircon ages define a 28·8–5·2 Maperiod of plutonic and volcanic activity that ceased as a consequenceof flattening subduction of the Nazca–Farallon plate.Rare earth elements patterns are variable, with up to 92 timeschondrite concentrations for light rare earth elements yielding(La/Yb)N between 3·6 and 7·0, and an absence ofEu anomalies. Initial Pb isotope signatures are in the rangeof 18·358–19·023 for 206Pb/ 204Pb, 15·567–15·700for 207Pb/ 204Pb and 38·249–39·084 for 208Pb/204Pb. Initial 87Sr/ 86Sr are mostly in the range of 0·70369–0·70505,with two more radiogenic values at 0·7066. Initial Hfisotopic compositions of zircons yield exclusively positiveHfi ranging between + 6·9 and + 9·6. The newlydetermined initial isotope characteristics of the Oligo-Miocenemagmas suggest that the mantle source lithologies are differentfrom both those of Pacific mid-ocean ridge basalt and oceanisland basalt, plotting in the field of reference values forsubcontinental lithospheric mantle, characterized by moderatelarge ion lithophile element–high field strengh elementdepletion and high 238U/ 204Pb. A Hf model age of 2 Ga is estimatedfor the formation of the subcontinental mantle–continentalcrust assemblage in the region, suggesting that the initialSr and Pb isotope ratios inferred for the source of the Oligo-Mioceneparental magmas are the result of later Rb and U enrichmentcaused by mantle metasomatism. A time-integrated model Rb/Srof 0·039 and µ 16 are estimated for the sourceof the parental magmas, consistent with ratios measured in peridotitexenoliths from continental areas. Evolution from predominant(>90%) basaltic–gabbroic to andesitic–dioriticmagmas seems to involve a combination of (1) original traceelement differences in the metasomatized subcontinental mantle,(2) different degrees of partial melting and (3) fractionalcrystallization in the garnet- and spinel-peridotite stabilityfields. The genesis of more differentiated magmas reaching rhyolitic–graniticcompositions most probably also includes additional crystalfractionation at both shallow mantle depths and within the crust,possibly leading to some very minor assimilation of crustalmaterial. KEY WORDS: calc-alkaline magmatism; Oligo-Miocene; U–Pb dating; Sr–Pb–Hf isotopes; central Chile  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.
Neogene plateau lavas in Patagonia, southern Argentina, eastof the volcanic gap between the Southern and Austral VolcanicZones at 46·5° and 49·5°S are linked withasthenospheric slab window processes associated with the collisionof a Chile Ridge segment with the Chile Trench at 12 Ma. Thestrong ocean-island basalt (OIB)-like geochemical signatures(La/Ta <20; Ba/La <20; 87Sr/86Sr = 0·7035–0·7046;143Nd/144Nd = 0·51290–0·51261; 206Pb/204Pb= 18·3–18·8; 207Pb/204Pb = 15·57–15·65;208Pb/204Pb = 38·4–38·7) of these Patagonianslab window lavas contrast with the mid-ocean ridge basalt (MORB)-like,depleted mantle signatures of slab window lavas elsewhere inthe Cordillera (e.g. Antarctic Peninsula; Baja California).The Patagonian lavas can be divided into a voluminous  相似文献   

14.
The Serbian province of Tertiary ultrapotassic volcanism isrelated to a post-collisional tectonic regime that followedthe closure of the Tethyan Vardar Ocean by Late Cretaceous subductionbeneath the southern European continental margin. Rocks of thisprovince form two ultrapotassic groups; one with affinitiesto lamproites, which is concentrated mostly in the central partsof the Vardar ophiolitic suture zone, and the other with affinitiesto kamafugites, which crops out in volcanoes restricted to thewestern part of Serbia. The lamproitic group is characterizedby a wide range of 87Sr/86Sri (0·70735–0·71299)and 143Nd/144Ndi (0·51251–0·51216), whereasthe kamafugitic group is isotopically more homogeneous witha limited range of 87Sr/86Sri (0·70599–0·70674)and 143Nd/144Ndi (0·51263–0·51256). ThePb isotope compositions of both groups are very similar (206Pb/204Pb18·58–18·83, 207Pb/204Pb 15·62–15·70and 208Pb/204Pb 38·74–38·99), falling withinthe pelagic sediment field and resembling Mesozoic flysch sedimentsfrom the Vardar suture zone. The Sr and Nd isotopic signaturesof the primitive lamproitic rocks correlate with rare earthelement fractionation and enrichment of most high field strengthelements (HFSE), and can be explained by melting of a heterogeneousmantle source consisting of metasomatic veins with phlogopite,clinopyroxene and F-apatite that are out of isotopic equilibriumwith the peridotite wall-rock. Decompression melting, with varyingcontributions from depleted peridotite and ultramafic veinsto the final melt, accounts for consistent HFSE enrichment andisotopic variations in the lamproitic group. Conversely, themost primitive kamafugitic rocks show relatively uniform Srand Nd isotopic compositions and trace element patterns, andsmall but regular variations of HFSE, indicating variable degreesof partial melting of a relatively homogeneously metasomatizedmantle source. Geochemical modelling supports a role for phlogopite,apatite and Ti-oxide in the source of the kamafugitic rocks.The presence of two contrasting ultrapotassic suites in a restrictedgeographical area is attributable to the complex geodynamicsituation involving recent collision of a number of microcontinentswith contrasting histories and metasomatic imprints in theirmantle lithosphere. The geochemistry of the Serbian ultrapotassicrocks suggests that the enrichment events that modified thesource of both lamproitic and kamafugitic groups were relatedto Mesozoic subduction events. The postcollisional environmentof the northern Balkan region with many extensional episodesis consistent at regional and local levels with the occurrenceof ultrapotassic rocks, providing a straightforward relationshipbetween geodynamics and volcanism. KEY WORDS: kamafugite; lamproite; Mediterranean; Serbia; mantle metasomatism; veined mantle; petrogenesis  相似文献   

15.
The spinel–garnet transition in Cr/Al-enriched peridotiticbulk compositions is known from experimental investigationsto occur at 20–70 kbar, within the pressure range sampledby kimberlites. We show that the Cr2O3–CaO compositionsof concentrate garnets from kimberlite have maximum Cr/Ca arrayscharacterized by Cr2O3/CaO 0·96–0·81, andinterpret the arrays as primary evidence of chromite–garnetcoexistence in Cr-rich harzburgitic or lherzolitic bulk compositionsderived from depth within the lithosphere. Under Cr-saturatedconditions on a known geotherm, each Cr/Ca array implicitlydelineates an isobar inside a garnet Cr2O3–CaO diagram.This simplification invites a graphical approach to calibratean empirical Cr/Ca-in-pyrope barometer. Carbonaceous chromite–garnetharzburgite xenoliths from the Roberts Victor kimberlite tightlybracket a graphite–diamond constraint (GDC) located atCr2O3 = 0·94CaO + 5·0 (wt %), representing a pivotalcalibration corresponding to 43 kbar on a 38 mW/m2 conductivegeotherm. Additional calibration points are established at 14,17·4 and 59·1 kbar by judiciously projecting garnetcompositions from simple-system experiments onto the same geotherm.The garnet Cr/Ca barometer is then simply formulated as follows(in wt %):
if Cr2O3 0·94CaO + 5, then P38 (kbar) = 26·9+ 3·22Cr2O3 – 3·03CaO, or
if Cr2O3 <0·94CaO + 5, then P38 (kbar) = 9·2+ 36[(Cr2O3+ 1·6)/(CaO + 7·02)].
A small correction to P38 values, applicable for 35–48mW/m2 conductive geotherms, is derived empirically by requiringconventional thermobarometry results and garnet concentratecompositions to be consistent with the presence of diamondsin the Kyle Lake kimberlite and their absence in the Zero kimberlite.We discuss application of the P38 barometer to estimate (1)real pressures in the special case where chromite–garnetcoexistence is known, (2) minimum pressures in the general casewhere Cr saturation is unknown, and (3) the maximum depth ofdepleted lithospheres, particularly those underlying Archaeancratons. A comparison with the PCr barometer of Ryan et al.(1996, Journal of Geophysical Research 101, 5611–5625)shows agreement with P38 at 55 ± 2 kbar, and 6–12%higher PCr values at lower P38. Because the PCr formulationsystematically overestimates the 43 kbar value of the GDC by2–6 kbar, we conclude that the empirical Cr/Ca-in-garnetbarometer is preferred for all situations where conductive geothermsintersect the graphite–diamond equilibrium. KEY WORDS: Cr-pyrope; chromite; P38 barometer; mantle petrology; lithosphere thickness  相似文献   

16.
Petrogenetic models for the origin of lamproites are evaluatedusing new major element, trace element, and Sr, Nd, and Pb isotopedata for Holocene lamproites from the Gaussberg volcano in theEast Antarctic Shield. Gaussberg lamproites exhibit very unusualPb isotope compositions (206Pb/204Pb = 17·44–17·55and 207Pb/204Pb = 15·56–15·63), which incommon Pb isotope space plot above mantle evolution lines andto the left of the meteorite isochron. Combined with very unradiogenicNd, such compositions are shown to be inconsistent with an originby melting of sub-continental lithospheric mantle. Instead,a model is proposed in which late Archaean continent-derivedsediment is subducted as K-hollandite and other ultra-high-pressurephases and sequestered in the Transition Zone (or lower mantle)where it is effectively isolated for 2–3 Gyr. The high207Pb/204Pb ratio is thus inherited from ancient continent-derivedsediment, and the relatively low 206Pb/204Pb ratio is the resultof a single stage of U/Pb fractionation by subduction-relatedU loss during slab dehydration. Sr and Nd isotope ratios, andtrace element characteristics (e.g. Nb/Ta ratios) are consistentwith sediment subduction and dehydration-related fractionation.Similar models that use variable time of isolation of subductedsediment can be derived for all lamproites. Our interpretationof lamproite sources has important implications for ocean islandbasalt petrogenesis as well as the preservation of geochemicallyanomalous reservoirs in the mantle. KEY WORDS: lamproites; Pb isotopes; mantle Transition Zone; subducted sediment; anomalous mantle reservoirs  相似文献   

17.
The Cretaceous lava sequence and associated mafic dyke swarmin central–western Madagascar (Mailaka and Bemaraha areas)range in composition from picrite basalts to cordierite–orthopyroxene-bearingrhyodacites (MgO from 14 to 0·6 wt %). Petrographic andchemical data indicate the presence of both tholeiitic and transitionalmagma series, with variable degree of rare earth element enrichment[(La/Nd)n = 1–1·4 for tholeiites vs (La/Nd)n =0·65–1 for transitional rocks]. Initial (at 88Ma) 87Sr/86Sr and  相似文献   

18.
Peridotites associated with pyroxenites (with rare olivine andspinel) are exposed on the islands of San Jorge and Santa Isabelin the Solomon Islands. Orthopyroxenite occurs in large outcrops(100 m2) whereas websterite and clinopyroxenite occur as layersand veins/dykes in peridotites. The bulk compositions of thepyroxenites are characterized by high Mg2+/(Mg2+ + Fe2+) (0·78–0·91)and low Al2O3 (<2·7 wt %). Low rare earth elementabundances are coupled with large ion lithophile element enrichmentsand positive Sr and Pb anomalies (primitive mantle-normalized)relative to adjacent rare earths. Temperatures of equilibrationfor the pyroxenites are between 950 and 1050°C. These relativelylow temperatures, combined with the occurrence of primary fluidinclusions, suggest that the pyroxenites formed by interactionof peridotite protoliths with an aqueous fluid. Bulk-rock andmineral compositions of the orthopyroxenites are similar tothose of mantle-derived pyroxenites, whereas the websteriteshave closer chemical affinity with crustal arc cumulates. Nevertheless,field relationships plus petrological, textural and geochemicalevidence are consistent with formation of all pyroxenite typesin supra-subduction zone mantle, resulting from metasomatismof peridotite by subducted Pacific Plate-derived fluid. Sucha setting for pyroxenite has not previously been reported indetail. We propose that these processes produce mantle pyroxenitewith compositions similar to crustal pyroxenite. KEY WORDS: mantle metasomatism; pyroxenite; supra-subduction zone  相似文献   

19.
Experimental studies were carried out to evaluate phase relationsinvolving titanite–F–Al-titanite solid solutionin the system CaSiO3–Al2SiO5–TiO2–CaF2. Theexperiments were conducted at 900–1000°C and 1·1–4·0GPa. The average F/Al ratio in titanite solid solution in theexperimental run products is 1·01 ± 0·06,and XAl ranges from 0·33 ± 0·02 to 0·91± 0·05, consistent with the substitution [TiO2+]–1[AlF2+]1.Analysis of the phase relations indicates that titanite solidsolutions coexisting with rutile are always low in XAl, whereasthe maximum XAl of titanite solid solution occurs with fluoriteand either anorthite or Al2SiO5. Reaction displacement experimentswere performed by adding fluorite to the assemblage anorthite+ rutile = titanite + kyanite. The reaction shifts from 1·60GPa to 1·15 ± 0·05 GPa at 900°C, from1·79 GPa to 1·375 ± 0·025 GPa at1000°C, and from 1·98 GPa to 1·575 ±0·025 GPa at 1100°C. The data show that the activityof CaTiSiO4O is very close to the ideal molecular activity model(XTi) at 1100°C, but shows a negative deviation at 1000°Cand 900°C. The results constrain  相似文献   

20.
Al2SiO5 reaction textures in aluminous schist and quartziteof the northern Picuris range, north-central New Mexico, recorda paragenetic sequence of kyanite to sillimanite to andalusite,consistent with a clockwise P–T loop, with minor decompressionnear the Al2SiO5 triple-point. Peak metamorphic temperaturesare estimated at 510–525°C, at 4·0–4·2kbar. Kyanite and fibrolite are strongly deformed; some prismaticsillimanite, and all andalusite are relatively undeformed. Monaziteoccurs as inclusions within kyanite, mats of sillimanite andcentimetre-scale porphyroblasts of andalusite, and is typicallyaligned subparallel to the dominant regional foliation (S0/S1or S2) and extension lineation (L1). Back-scatter electron imagesand X-ray maps of monazite reveal distinct core, intermediateand rim compositional domains. Monazite–xenotime thermometryfrom the intermediate and rim domains yields temperatures of405–470°C (±50°C) and 500–520°C(±50°C), respectively, consistent with the progradeto peak metamorphic growth of monazite. In situ, ion microprobeanalyses from five monazites yield an upper intercept age of1417 ± 9 Ma. Near-concordant to concordant analyses yield207Pb–206Pb ages from 1434 ± 12 Ma (core) to 1390± 20 Ma (rim). We find no evidence of older regionalmetamorphism related to the 1650 Ma Mazatzal Orogeny. KEY WORDS: Al2SiO5; metamorphism; monazite; thermochronometry; triple-point  相似文献   

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