Systematic Variation of Sr-, Nd- and Pb-Isotopes with Time in Lavas of Mauritius, Reunion Hotspot

We report Sr-, Nd- and Pb-isotopic compositions for the lavasof Mauritius, the second youngest volcanic island in the Réunionhotspot. The lavas of the Older Series (7·8–5·5Ma) have identical isotopic compositions (⁸⁷Sr/⁸⁶Sr = 0·70411to 0·70422,¹⁴³Nd/¹⁴⁴Nd = 0·512865 to 0·512854,and ²⁰⁶Pb/²⁰⁴Pb = 19·016 to 19·041) to those ofRéunion, where the center of volcanic activity is currentlylocated. The lavas of the Intermediate Series (3·5–1·9Ma) and Younger Series (0·70–0·17 Ma) areshifted to lower Sr-isotopic compositions (0·70364–0·70394,with ¹⁴³Nd/¹⁴⁴Nd = 0·512813 to 0·512948 and ²⁰⁶Pb/²⁰⁴Pb= 18·794 to 18·984). The Intermediate Series lavashave similar trace-element characteristics (e.g. Zr–Nb,Ba–Y) to those of Rodrigues, in both cases requiring theinvolvement of an enriched mantle-like component in the mantlesource. During the volcanic history of Mauritius, the magmaslost the principal isotopic characteristics of the Réunionhotspot with time, and became gradually imprinted with the isotopicsignature of a shallower mantle source that produced the CentralIndian Ridge basalts. KEY WORDS: hotspot; isotopes; Mauritius; Réunion; trace element     

Mantle Processes and Sources of Neogene Slab Window Magmas from Southern Patagonia, Argentina

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     

Sr, Nd, Pb and O Isotopes of Minettes from Schirmacher Oasis, East Antarctica: a Case of Mantle Metasomatism involving Subducted Continental Material

Numerous minette dykes intersect the Precambrian crystallinebasement of Schirmacher Oasis, East Antarctica. This study presentsnew Sr, Nd, Pb and O isotope data for 11 minette samples fromfour different dykes. The samples are characterized by relativelyhigh ⁸⁷Sr/⁸⁶Sr (0·7077–0·7134), ²⁰⁷Pb/²⁰⁴Pb(15·45–15·55) and ²⁰⁸Pb/²⁰⁴Pb (37·8–39·8),combined with low ¹⁴³Nd/¹⁴⁴Nd (     

The Origin of HIMU in the SW Pacific: Evidence from Intraplate Volcanism in Southern New Zealand and Subantarctic Islands

This paper presents field, geochemical and isotopic (Sr, Nd,Pb) results on basalts from the Antipodes, Campbell and ChathamIslands, New Zealand. New ⁴⁰Ar/³⁹Ar age determinations alongwith previous K–Ar dates reveal three major episodes ofvolcanic activity on Chatham Island (85–82, 41–35,5 Ma). Chatham and Antipodes samples comprise basanite, alkaliand transitional basalts that have HIMU-like isotopic (²⁰⁶Pb/²⁰⁴Pb>20·3–20·8, ⁸⁷Sr/⁸⁶Sr <0·7033,¹⁴³Nd/¹⁴⁴Nd >0·5128) and trace element affinities(Ce/Pb 28–36, Nb/U 34–66, Ba/Nb 4–7). Thegeochemistry of transitional to Q-normative samples from CampbellIsland is explained by interaction with continental crust. Thevolcanism is part of a long-lived (100 Myr), low-volume, diffusealkaline magmatic province that includes deposits on the Northand South Islands of New Zealand as well as portions of WestAntarctica and SE Australia. All of these continental areaswere juxtaposed on the eastern margin of Gondwanaland at >83Ma. A ubiquitous feature of mafic alkaline rocks from this regionis their depletion in K and Pb relative to other highly incompatibleelements when normalized to primitive mantle values. The inversionof trace element data indicates enriched mantle sources thatcontain variable proportions of hydrous minerals. We proposethat the mantle sources represent continental lithosphere thathost amphibole/phlogopite-rich veins formed by plume- and/orsubduction-related metasomatism between 500 and 100 Ma. Thestrong HIMU signature (²⁰⁶Pb/²⁰⁴Pb >20·5) is consideredto be an in-grown feature generated by partial dehydration andloss of hydrophile elements (Pb, Rb, K) relative to more magmaphileelements (Th, U, Sr) during short-term storage at the base ofthe lithosphere. KEY WORDS: continental alkaline basalts; lithospheric mantle, mantle metasomatism; New Zealand; OIB, HIMU; Sr, Nd and Pb isotopes; West Antarctica     

Petrogenesis of Pre-caldera Mafic Lavas, Jemez Mountains Volcanic Field (New Mexico, USA)

The Miocene–Quaternary Jemez Mountains volcanic field(JMVF), the site of the Valles caldera, lies at the intersectionof the Jemez lineament, a Proterozoic suture, and the CenozoicRio Grande rift. Parental magmas are of two types: K-depletedsilica-undersaturated, derived from the partial melting of lithosphericmantle with residual amphibole, and tholeiitic, derived fromeither asthenospheric or lithospheric mantle. Variability insilica-undersaturated basalts reflects contributions of meltsderived from lherzolitic and pyroxenitic mantle, representingheterogeneous lithosphere associated with the suture. The Kdepletion is inherited by fractionated, crustally contaminatedderivatives (hawaiites and mugearites), leading to distinctiveincompatible trace element signatures, with Th/(Nb,Ta) and La/(Nb,Ta)greater than, but K/(Nb,Ta) similar to, Bulk Silicate Earth.These compositions dominate the mafic and intermediate lavas,and the JMVF is therefore derived largely, and perhaps entirely,from melting of fertile continental Jemez lineament lithosphereduring rift-related extension. Significant variations in Pband Nd isotope ratios (²⁰⁶Pb/²⁰⁴Pb = 17·20–18·93;¹⁴³Nd/¹⁴⁴Nd = 0·51244–0·51272) result fromcrustal contamination, whereas ⁸⁷Sr/⁸⁶Sr is low and relativelyuniform (0·7040–0·7048). We compare theeffects of contamination by low-⁸⁷Sr/⁸⁶Sr crust with assimilationof high-⁸⁷Sr/⁸⁶Sr granitoid by partial melting, with Sr retainedin a feldspathic residue. Both models satisfactorily reproducethe isotopic features of the rocks, but the lack of a measurableEu anomaly in most JMVF mafic lavas is difficult to reconcilewith a major role for residual plagioclase during petrogenesis. KEY WORDS: Jemez Mountains volcanic field; Rio Grande rift; lithospheric mantle; crustal contamination; trace elements; radiogenic isotopes     

Sampling the Cape Verde Mantle Plume: Evolution of Melt Compositions on Santo Antao, Cape Verde Islands

The volcanic history of Santo Antão, NW Cape Verde Islands,includes the eruption of basanite–phonolite series magmasbetween 7·5 and 0·3 Ma and (melilite) nephelinite–phonoliteseries magmas from 0·7 to 0·1 Ma. The most primitivevolcanic rocks are olivine ± clinopyroxene-phyric, whereasthe more evolved rocks have phenocrysts of clinopyroxene ±Fe–Tioxide ± kaersutite ± haüyne ± titanite± sanidine; plagioclase occurs in some intermediate rocks.The analysed samples span a range of 19–0·03% MgO;the most primitive have 37–46% SiO₂, 2·5–7%TiO₂ and are enriched 50–200 x primitive mantle in highlyincompatible elements; the basanitic series is less enrichedthan the nephelinitic series. Geochemical trends in each seriescan be modelled by fractional crystallization of phenocrystassemblages from basanitic and nephelinitic parental magmas.There is little evidence for mineral–melt disequilibrium,and thus magma mixing is not of major importance in controllingbulk-rock compositions. Mantle melting processes are modelledusing fractionation-corrected magma compositions; the modelssuggest 1–4% partial melting of a heterogeneous mantleperidotite source at depths of 90–125 km. Incompatibleelement enrichment among the most primitive magma types is typicalof HIMU OIB. The Sr, Nd and Pb isotopic compositions of theSanto Antão volcanic sequence and geochemical characterchange systematically with time. The older volcanic rocks (7·5–2Ma) vary between two main mantle source components, one of whichis a young HIMU type with ²⁰⁶Pb/²⁰⁴Pb = 19·88, 7/4 =–5, 8/4 0, ⁸⁷Sr/⁸⁶Sr = 0·7033 and ¹⁴³Nd/¹⁴⁴Nd= 0·51288, whereas the other has somewhat less radiogenicSr and Pb and more radiogenic Nd. The intermediate age volcanicrocks (2–0·3 Ma) show a change of sources to two-componentmixing between a carbonatite-related young HIMU-type source(²⁰⁶Pb/²⁰⁴Pb = 19·93, 7/4 = –5, 8/4 = –38,⁸⁷Sr/⁸⁶Sr = 0·70304) and a DM-like source. A more incompatibleelement-enriched component with 7/4 > 0 (old HIMU type) isprominent in the young volcanic rocks (0·3–0·1Ma). The EM1 component that is important in the southern CapeVerde Islands appears to have played no role in the petrogenesisof the Santo Antão magmas. The primary magmas are arguedto be derived by partial melting in the Cape Verde mantle plume;temporal changes in composition are suggested to reflect layeringin the plume conduit. KEY WORDS: radiogenic isotopes; geochemistry; mantle melting; Cape Verde     

Generation of Palaeocene Adakitic Andesites by Magma Mixing; Yanji Area, NE China

Palaeocene (c. 55–58 Ma) adakitic andesites from the Yanjiarea, NE China, are typically clinopyroxene-bearing sodic andesitescontaining 60· 9–62· 2% SiO₂ and 4·02–4· 36% MgO, with high Mg-number [100 Mg/(Mg+ Fe) atomic ratio] from 65· 5 to 70· 1. Whole-rockgeochemical features include high Cr (128–161 ppm) andNi (86–117 ppm) concentrations, extremely high Sr (2013–2282ppm), low Y (10–11 ppm) and heavy rare earth elements(HREE; e.g. Yb = 0· 79–1· 01 ppm), and mid-oceanridge basalt (MORB)-like Sr–Nd–Pb isotopic compositions[e.g. ⁸⁷Sr/ ⁸⁶Sr(i) = 0· 70298–0· 70316,_Nd(t) = +3· 8 to +6· 3 and ²⁰⁶Pb/ ²⁰⁴Pb = 17·98 – 18· 06], analogous to high-Mg adakites occurringin modern subduction zones. However, mineralogical evidencefrom clinopyroxene phenocrysts and microcrystalline plagioclaseclearly points to magma mixing during magma evolution. Iron-richclinopyroxene (augite) cores with low Sr, high Y and heavy REEcontents, slightly fractionated REE patterns and large negativeEu anomalies probably crystallized along with low-Ca plagioclasefrom a lower crustal felsic magma. In contrast, high Mg-numberclinopyroxene (diopside and endiopside) mantles and rims havehigher Sr and lower HREE and Y concentrations, highly fractionatedREE patterns (high La/Yb) and negligible Eu anomalies, similarto those found in adakites from subduction zones. The Yanjiadakitic andesites can be interpreted as a mixture between acrust-derived magma having low Mg-number and Sr, and high Yand HREE, and a mantle-derived high Mg-number adakite havinghigh Sr and low Y and HREE concentrations. During storage and/orascent, the mixed magma experienced further crustal contaminationto capture zircons, of a range of ages, from the wall rocks.The absence of coeval arc magmatism and an extensional tectonicregime in the Yanji area and surrounding regions suggest thatthese Palaeocene adakitic andesites were formed during post-subductionextension that followed the late Cretaceous Izanagi–Farallonridge subduction. Generation of these adakitic andesites doesnot require contemporaneous subduction of a young, hot oceanicridge or delamination of eclogitic lower crust as suggestedby previous models. KEY WORDS: magma mixing; adakitic andesites; Palaeocene; NE China     

Petrology and Geochemistry of Intraplate Basalts in the South Auckland Volcanic Field, New Zealand: Evidence for Two Coeval Magma Suites from Distinct Sources

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     

Petrogenesis of the Largest Intraplate Volcanic Field on the Arabian Plate (Jordan): a Mixed Lithosphere-Asthenosphere Source Activated by Lithospheric Extension

Miocene to Recent volcanism in northwestern Arabia producedthe largest intraplate volcanic field on the Arabian plate (HarratAsh Shaam, Jordan). The chemically and isotopically diversevolcanic field comprises mafic alkali basalts and basanites.The magmas underwent limited fractional crystallization of ol± cpx ± plag and rare samples have assimilatedup to 20% of Late Proterozoic crust en route to the surface.However, there are subtle Sr–Nd–Pb isotopic variations(⁸⁷Sr/⁸⁶Sr = 0·70305–0·70377, ¹⁴³Nd/¹⁴⁴Nd= 0·51297–0·51285, ²⁰⁶Pb/²⁰⁴Pb = 18·8–19·2),which exhibit marked correlations with major elements, incompatibletrace element ratios and abundances in relatively primitivebasalts (MgO >8·5 wt %), and cannot be explained byfractional crystallization and crustal contamination alone.Instead, the data require polybaric melting of heterogeneoussources. Semi-quantitative melt modelling suggests that thisheterogeneity is the result of small degree melts (2–5%)from spinel- and garnet-facies mantle, inferred to be shallowArabian lithosphere, that mixed with smaller degree melts (<1%)from a predominantly deep garnet-bearing asthenospheric(?) sourcewith ocean island basalt characteristics. The latter may bea ubiquitous part of the asthenosphere but is preferentiallytapped at small degrees of partial melting. Volcanism in Jordanappears to be the result of melting lithospheric mantle in responseto lithospheric extension. With time, thinning of the lithosphereallowed progressively deeper mantle (asthenosphere?) to be activatedand melts from this to mix with the shallower lithospheric mantlemelts. Although Jordanian intraplate volcanism is isotopicallysimilar to examples of Late Cenozoic volcanism throughout theArabian peninsula (Israel, Saudi Arabia), subtle chemical andisotopic differences between Yemen and Jordan intraplate volcanismsuggest that the Afar plume has not been channelled northwestwardsbeneath the Arabian plate and played no role in producing thenorthern Saudi Arabian and Jordan intraplate volcanic fields. KEY WORDS: asthenosphere; intraplate volcanism; Jordan; lithospheric mantle; Sr–Nd–Pb isotopes     

Lamproitic Rocks from a Continental Collision Zone: Evidence for Recycling of Subducted Tethyan Oceanic Sediments in the Mantle Beneath Southern Tibet

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     

The Role of Continental Crust and Lithospheric Mantle in the Genesis of Cameroon Volcanic Line Lavas: Constraints from Isotopic Variations in Lavas and Megacrysts from the Biu and Jos Plateaux

We present a combined Sr, Nd, Pb and Os isotope study of lavasand associated genetically related megacrysts from the Biu andJos Plateaux, northern Cameroon Volcanic Line (CVL). Comparisonof lavas and megacrysts allows us to distinguish between twocontamination paths of the primary magmas. The first is characterizedby both increasing ²⁰⁶Pb/²⁰⁴Pb (19·82–20·33)and ⁸⁷Sr/⁸⁶Sr (0·70290–0·70310), and decreasing_Nd (7·0–6·0), and involves addition of anenriched sub-continental lithospheric mantle-derived melt. Thesecond contamination path is characterized by decreasing ²⁰⁶Pb/²⁰⁴Pb(19·82–19·03), but also increasing ⁸⁷Sr/⁸⁶Sr(0·70290–0·70359), increasing ¹⁸⁷Os/¹⁸⁸Os(0·130–0·245) and decreasing _Nd (7·0–4·6),and involves addition of up to 8% bulk continental crust. Isotopicsystematics of some lavas from the oceanic sector of the CVLalso imply the involvement of a continental crustal component.Assuming that the line as a whole shares a common source, wepropose that the continental signature seen in the oceanic sectorof the CVL is caused by shallow contamination, either by continent-derivedsediments or by rafted crustal blocks that became trapped inthe oceanic lithosphere during continental breakup in the Mesozoic. KEY WORDS: crustal contamination; CVL; megacrysts; ocean floor; osmium isotopes     

Tertiary Ultrapotassic Volcanism in Serbia: Constraints on Petrogenesis and Mantle Source Characteristics

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/⁸⁶Sr_i (0·70735–0·71299)and ¹⁴³Nd/¹⁴⁴Nd_i (0·51251–0·51216), whereasthe kamafugitic group is isotopically more homogeneous witha limited range of ⁸⁷Sr/⁸⁶Sr_i (0·70599–0·70674)and ¹⁴³Nd/¹⁴⁴Nd_i (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     

Combined Trace Element and Pb-Nd-Sr-O Isotope Evidence for Recycled Oceanic Crust (Upper and Lower) in the Iceland Mantle Plume

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 ¹⁸O_olivine 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     

Geochemical Evolution of Akagi Volcano, NE Japan: Implications for Interaction Between Island-arc Magma and Lower Crust, and Generation of Isotopically Various Magmas

Major and trace element, and Sr, Nd and Pb isotopic compositionswere determined for whole-rock samples from the ‘isotopicallyanomalous’ Akagi volcano in the volcanic front of theNE Japan arc. Sr and Nd isotopic compositions of phenocrystswere also analyzed together with their major and trace elementcompositions. Compared with the other volcanoes from the volcanicfront, the whole-rock isotope compositions of Akagi show highlyenriched characteristics; ⁸⁷Sr/⁸⁶Sr = 0·7060–0·7088,     

A North-South Transect across the Central Mexican Volcanic Belt at ~100{degrees}W: Spatial Distribution, Petrological, Geochemical, and Isotopic Characteristics of Quaternary Volcanism

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     

Kistufell: Primitive Melt from the Iceland Mantle Plume

This paper presents new geochemical data from Kistufell (64°48'N,17°13'W), a monogenetic table mountain situated directlyabove the inferred locus of the Iceland mantle plume. Kistufellis composed of the most primitive olivine tholeiitic glassesfound in central Iceland (MgO 10·56 wt %, olivine Fo_89·7).The glasses are interpreted as near-primary, high-degree plumemelts derived from a heterogeneous mantle source. Mineral, glassand bulk-rock (glass + minerals) chemistry indicates a low averagemelting pressure (15 kbar), high initial crystallization pressuresand temperatures (10–15 kbar and 1270°C), and eruptiontemperatures (1240°C) that are among the highest observedin Iceland. The glasses have trace element signatures (La_n/Yb_n<1, Ba_n/Zr_n 0·55–0·58) indicative ofa trace element depleted source, and the Sr–Nd–Pbisotopic ratios (⁸⁷Sr/⁸⁶Sr 0·70304–0·70308,¹⁴³Nd/¹⁴⁴Nd 0·513058–0·513099, ²⁰⁶Pb/²⁰⁴Pb18·343–18·361) further suggest a long-termtrace element depletion relative to primordial mantle. HighHe isotopic ratios (15·3–16·8 R/R_a) combinedwith low ²⁰⁷Pb/²⁰⁴Pb (15·42–15·43) suggestthat the mantle source of the magma is different from that ofNorth Atlantic mid-ocean ridge basalt. Negative Pb anomalies,and positive Nb and Ta anomalies indicate that the source includesa recycled, subducted oceanic crustal or mantle component. PositiveSr anomalies (Sr_n/Nd_n = 1·39–1·50) furthersuggest that this recycled source component involves lower oceaniccrustal gabbros. The     

Isotopic and Geochemical Investigation of the Chilwa Island Carbonatite Complex, Malawi: Evidence for a Depleted Mantle Source Region, Liquid Immiscibility, and Open-System Behaviour

Initial Nd, Pb, and Sr isotopic data from carbonatites and associatedintrusive silica-undersaturated rocks from the early Jurassic,Chilwa Island complex, located in southern Malawi, central Africa,suggest melt derivation from a Rb/Sr- and Nd/Sm-depleted butTh/Pb- and U/Pb-enriched mantle source. Initial ¹⁴³Nd/¹⁴⁴Nd(0.51265–0.51270) isotope ratios from the Chilwa Islandcarbonatites are relatively constant, but their initial ⁸⁷Sr/⁸⁶Sr(0.70319–0.70361) ratios are variable. The ¹⁸O_smow (9.53–14.15%0)and ¹³C_PDB (–3.27 to –1.50%0) isotope ratios ofthe carbonates are enriched relative to the range of mantlevalues, and there is a negative correlation between ¹⁸O andSr isotope ratios. The variations in Sr, C, and O isotopic ratiosfrom the carbonatites suggest secondary processes, such as interactionwith meteoric groundwater during late-stage carbonatite activity.The initial ¹⁴³Nd/¹⁴⁴Nd (0.51246 0.51269) and initial ⁸⁷Sr/⁸⁶Sr(0.70344–0.70383) isotope ratios from the intrusive silicaterocks are more variable, and the Sr more radiogenic than thosefrom the carbonatites. Most of the Pb isotope data from Chilwa Island plot to the rightof the geochron and close to the oceanic regression line definedby MORBs and OIBs. Initial Pb isotopic ratios from both carbonatites(²⁰⁷Pb/²⁰⁴Pb 15.63–15.71; ²⁰⁶Pb/²⁰⁴Pb 19.13–19.78)and silicate rocks (²⁰⁷Pb/²⁰⁴Pb 15.61–15.72; ²⁰⁶Pb/²⁰⁴Pb18.18–20.12) show pronounced variations, and form twogroups in Pb-Pb plots. The isotopic variations shown by Nd, Pb, and Sr for the ChilwaIsland carbonatites and intrusive silicates suggest that thesemelts underwent different evolutionary histories. The chemicaldata, including isotopic ratios, from the carbonatites and olivinenephelinites are consistent with magmatic differentiation ofa carbonated-nephelinite magma. A model is proposed in whichdifferentiation of the carbonatite magma was accompanied byfenitization (metasomatic alteration) of the country rocks bycarbonatite-derived fluids, and subsequent alteration of thecarbonatite by hydrothermal activity. The chemical and isotopicdata from the non-nephelinitic intrusive silicate rocks reveala more complex evolutionary history, involving either selectivebinary mixing of lower-crustal granulites and a nephelinitemagma, or incremental batch melting of a depleted source andsubsequent crustal contamination.     

Carbonatite Magmatism and Plume Activity: Implications from the Nd, Pb and Sr Isotope Systematics of Oldoinyo Lengai

New Nd (0.51261–0.51268), Pb (²⁰⁶Pb/²⁰⁴Pb: 19.24–19.26),and Sr (0.70437–0.70446) isotopic compositions from tennatrocarbonatite lavas, collected in June 1993 from OldoinyoLengai, the only known active carbonatite volcano, are relativelyuniform, and are similar to data from the 1960 and 1988 flows.Three of the samples contain silicate spheroids, one of whichhas Nd and Sr isotopic ratios similar to host natrocarbonatite,consistent with an origin by liquid immiscibility or the mixingof melts with similar isotopic compositions. Pb isotope datafor two samples of trona are inconsistent with its involvementin the genesis of natrocarbonatite. New Pb isotope data fromsilicate volcanic and plutonic blocks (ijolite, nephelinite,phonolite, syenite) from Oldoinyo Lengai are highly variable(²⁰⁶Pb/²⁰⁴Pb, 17.75–19.34; ²⁰⁷Pb/²⁰⁴Pb, 15.41–15.67;²⁰⁸Pb/²⁰⁴Pb, 37.79–39.67), and define near-linear arraysin Pb-Pb diagrams. The isotopic data for the silicate rocksfrom Oldoinyo Lengai are best explained by invoking discretepartial melting events which generate undersaturated alkalinesilicate magmas with distinct isotopic ratios. Pb isotope ratiosfrom most ijolites and phonolites are predominantly lower andmore variable than from the natrocarbonatites, and are attributedto interaction between silicate melts involving HIMU and EMIsource components and an additional component, such as lower-crustalgranulites, DMM or PREMA (prevalent mantle). Variations in Nd,Pb and Sr isotope ratios from Oldoinyo Lengai, among the largestyet documented from a single volcano, are attributed to mantlesource heterogeneity involving mainly the mixing of HIMU andEMI mantle components. Based on the new isotopic data from OldoinyoLengai and data from other East African carbonatites, and mantlexenoliths, we propose a two-stage model in an attempt to explainthe isotope variations shown by carbonatites in this area. Themodel involves (I) the release of metasomatizing agents withHIMU-like signatures from upwelling mantle (‘plume’)source, which in turn metasomatize the sub-continental (old,isotopically enriched, EMI-like) lithosphere, and (2) variabledegrees and discrete partial melting of the resulting heterogeneous,metasomatized lithosphere. KEY WORDS: carbonatite; isotopes; Oldoinyo Lengai; mantle plumes ^*Telephone: (613) 788–2660, ext. 4419. Fax: (613) 788–4490. e-mail: kbell{at}ccs.carleton.ca     

Petrology and Geochemistry of Eclogite Xenoliths from the Colorado Plateau: Implications for the Evolution of Subducted Oceanic Crust

Eclogite xenoliths from the Colorado Plateau, interpreted asfragments of the subducted Farallon plate, are used to constrainthe trace element and Sr–Nd–Pb isotopic compositionsof oceanic crust subducted into the upper mantle. The xenolithsconsist of almandine-rich garnet, Na-clinopyroxene, lawsoniteand zoisite with minor amounts of phengite, rutile, pyrite andzircon. They have essentially basaltic bulk-rock major elementcompositions; their Na₂O contents are significantly elevated,but K₂O contents are similar to those of unaltered mid-oceanridge basalt (MORB). These alkali element characteristics areexplained by spilitization or albitization processes on thesea floor and during subduction-zone metasomatism in the fore-arcregion. The whole-rock trace element abundances of the xenolithsare variable relative to sea-floor-altered MORB, except forthe restricted Zr/Hf ratios (36·9–37·6).Whole-rock mass balances for two Colorado Plateau eclogite xenolithsare examined for 22 trace elements, Rb, Cs, Sr, Ba, Y, rareearth elements, Pb, Th and U. Mass balance considerations andmineralogical observations indicate that the whole-rock chemistriesof the xenoliths were modified by near-surface processes afteremplacement and limited interaction with their host rock, aserpentinized ultramafic microbreccia. To avoid these secondaryeffects, the Sr, Nd and Pb isotopic compositions of mineralsseparated from the xenoliths were measured, yielding 0·70453–0·70590for ⁸⁷Sr/⁸⁶Sr, –3·1 to 0·5 for Nd and 18·928–19·063for ²⁰⁶Pb/²⁰⁴Pb. These isotopic compositions are distinctlymore radiogenic for Sr and Pb and less radiogenic for Nd thanthose of altered MORB. Our results suggest that the MORB-likeprotolith of the xenoliths was metasomatized by a fluid equilibratedwith sediment in the fore-arc region of a subduction zone andthat this metasomatic fluid produced continental crust-likeisotopic compositions of the xenoliths. KEY WORDS: Colorado Plateau; eclogite xenolith; geochemistry; subducted oceanic crust     

Crustal Assimilation as a Major Petrogenetic Process in the East Carpathian Neogene and Quaternary Continental Margin Arc, Romania

Miocene to Pleistocene calc-alkaline volcanism in the East Carpathianarc of Romania was related to the subduction of a small oceanbasin beneath the continental Tisza–Dacia microlate. Volcanicproducts are predominantly andesitic to dadtic in composition,with rare basalts and rhyodacites (51–l71% SiO₂; mg-number0.65–0.26) and have medium- to high-K calcalkaline andshoshonitic affinities. Mg, Cr and Ni are low in all rock-types,indicating the absence of primary erupted compositions. Detailedtrace element and Sr, Nd, Pb and 0 isotope data suggest thatmagmas were strongly crustally contaminated. Assimilation andfractional crystallization (AFC) calculations predict the consumptionof 5–35% local upper-crustal metasediments or sedimentsfrom the palaeo-accretionary wedge. Variations in the isotopiccomposition of the contaminants and parental magmas caused variationsin the mixing trajectories in different parts of the arc Themost primitive isotopic compositions are found in low-K dacitesof the northern Cdlimani volcanic centre and are interpretedas largely mantle derived. A second possible mantle reservoirof lower ¹⁴⁹ Nd/¹⁴⁴ Nd and lower ²⁰⁶ Pb/²⁰⁴ Pb is identifiedfrom back-arc basic calc-alkaline rocks in the south of thearc Both magmatic reservoirs have elevated isotopic characteristics,owing either to source bulk mixing (between depleted or enrichedasthenosphere and <1% average subducted local sediment) orlower-crustal contamination. KEY WORDS: Carpathians; assimilation; calc-alkaline; Sr-Nd-Pb-0 isotopes; laser flurination