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     

Ultramafic Xenoliths in Plio-Pleistocene Alkali Basalts from the Eastern Transylvanian Basin: Depleted Mantle Enriched by Vein Metasomatism

Ultramafic xenoliths from alkali basalts in the Perjani Mountainsin the Eastern Transylvanian Basin (ETB) of Romania are mainlyspinel Iherzolites, although spinel harzburgites, websterites,clinopyroxenites and amphibole pyroxenites are also present.Amphibole veins cut some spinel peridotite samples. All arederived from the shallow lithospheric upper mantle. In general,textural variations are restricted to protogranular and porphyroclastictypes, compared with the more varied textures found in mantlexenoliths from the alkali basalts of the neighbouring PannonianBasin. Also, ETB peridotites are richer in amphibole. Thus,the mantle beneath the edge of the ETB is less deformed butmore strongly metasomatized than the mantle closer to the centreof the Pannonian Basin.Mineralogical and bulk-rock geochemicalvariations resemble those of spinel Iherzolites from other sub-continentalshallow mantle xenolith suites. There is no apparent correlationbetween deformation and geochemistry, and much of the majorand trace element variation is due to variable extraction ofpicritic melts. The REE patterns of separated clinopyroxenesfrom the peridotite xenoliths are mostly LREE depleted, althoughclinopyroxenes from regions adjacent to amphibole veins haveexperienced an enrichment in La and Ce and a change in theirSr and Nd isotopic values towards those of the vein, while stillretaining an overall LREE depletion. Clinopyroxenes from thewebsterites and clinopyroxenites are more variable. Amphibolein the hydrous pyroxenites and amphibole veins is strongly LREEenriched and is considered to be metasomatic in origin. ⁸⁷Sr/⁸⁶Srand ¹⁴³Nd/^l44Nd isotopic ratios of the xenoliths vary between07018 and 07044, and 051355 and 0 51275, respectively. Thesevalue are more depleted than those obtained for xenoliths fromthe Pannonian Basin. The lower ^l43Nd/^l44Nd and higher ⁸⁷Sr/Sr⁸⁶values are found in anhydrous pyroxenites, metasomatic amphibolesin veins and amphibole pyroxenites, and in the only exampleof an equigranular spinel Iherzolite in the suite.The ETB xenolithswere brought to the surface in alkaline vokanism which post-dateda period of Miocene to Pliocene subduction-related cak-alkalinevolcanism. However, the effects of the passage of either slab-derivedfluids or cak-alkaline magmas through the ETB lithospheric mantlecannot be discerned in the chemistry of the xenoliths. The metasomaticamphibole has ⁸⁷Sr/Sr⁸⁶ and ¹⁴³Sr/Sr¹⁴⁴ ratios similar to thehost alkali basalts, but the least evoked cak-alkaline magmasalso have similar Sr and Nd isotope compositions. The REE patternsof the amphibole resembk those of amphiboles considered to havecrystallized from alkaline melts. No preferential enrichmentin elements typically associated with slab-derivedfluids (K,Rb and Sr) relative to elements typically depleted in cak-alkalinemagmas (Ti, 2jr and Nb) has been observed in the vein amphiboles,although some interstitial amphibole is depleted in all incompatibletrace elements, including LREE. Thus, despite its position closeto the calc-alkaline volcanic arc of the Eastern Carpathians,we cannot readily detect any interaction between the lithosphericupper mantle beneath the ETB and subduction-related magmas orfluids. Metasomatism in the lithospheric mantle is instead largelyrelated to the passage of a primitive alkaline magma similarto the host alkali basal ^*corresponding author     

Constraints on the Source Components of Lavas Forming the Hawaiian North Arch and Honolulu Volcanics

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     

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 Early-Orogenic Diorites, Tonalites and Post-Orogenic Trondhjemites in the Nubian Shield

The gabbro-diorite-quartz diorite-tonalite (GDT) suite representsthe oldest crustal component in northeastern Egypt; it was emplacedat 881?58 Ma during the early stage of the Pan-African orogeny.Renewed tectono-magmatic processes at the post-orogenic stageproduced the 516?7 Ma trondhjemite (TR) suite that was emplacedinto GDT host rocks. The GDT suite is compositionally broad,with a wide range of SiO₂ contents (50–64 wt.%), and isdepleted in K, Rb, Y, Nb, Hf, and REE. The suite shows a smoothvariation in both major and trace elements from gabbro to tonaliteand has a very low Rb/Sr ratio (0?05) and a low initial ⁸⁷Sr/⁸⁶Srratio (0?7042). It is calc-alkaline and shows the petrologicalcharacteristics of M-type granites and the trace-element characteristicsof arc-lavas. The GDT suite exhibits REE profiles typical ofisland-arc basalt (IAB), with an (La/Yb)_N ratio of 5?5. The trondhjemite is a relatively homogeneous felsic unit (71–75wt. % SiO₂) and belongs to the high- Al₂O₃ continental trondhjemitetype. The TR has a low Rb/Sr ratio (0?16), a low Sr-initialratio (0?7047) and trace-element characteristics of volcanic-arcgranites. It is relatively enriched in Al, Sr, and Ba, depletedin K and Rb, and highly depleted in Y, Nb, Zr, Hf, Ta, and REE,with LREE-depleted, less fractionated patterns [(La/Yb)_N=5?3].These features suggest that the TR was derived from a geochemicallyprimitive source. The GDT suite resulted first by the emplacement of a gabbroicmagma, derived possibly from a mantle wedge above an early Pan-Africansubduction zone, and fractionated (48?8% plagioclase, 12?4%augite, 22% amphibole, and 2?9% magnetite, as documented byfractionation modelling) to give the more felsic varieties.Petrogenetic modelling, combined with petrographic and geochemicalfeatures, suggests that the TR magma was produced by non-modalpartial melting of GDT rocks at depth; fractional crystallizationof plagioclase and amphibole controlled the evolution of thisTR magma. This and other studies suggest that post-Archean trondhjemitesare similar to Archean trondhjemites in that they were mostlyproduced via multi-stage development and crustal recycling whichinvolved partial melting of a mafic crustal source.     

The Cretaceous Igneous Province of Madagascar: Geochemistry and Petrogenesis of Lavas and Dykes from the Central-Western Sector

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     

Petrogenesis of Tertiary Continental Intra-plate Lavas from the Westerwald Region, Germany

Tertiary volcanic rocks from the Westerwald region range frombasanites and alkali basalts to trachytes, whereas lavas fromthe margin of the Vogelsberg volcanic field consist of morealkaline basanites and alkali basalts. Heavy rare earth elementfractionation indicates that the primitive Westerwald magmasprobably represent melts of garnet peridotite. The Vogelsbergmelts formed in the spinel–garnet peridotite transitionregion with residual amphibole for some magmas suggesting meltingof relatively cold mantle. Assimilation of lower-crustal rocksand fractional crystallization altered the composition of lavasfrom the Westerwald and Vogelsberg region significantly. Thecontaminating lower crust beneath the Rhenish Massif has a differentisotopic composition from the lower continental crust beneaththe Hessian Depression and Vogelsberg, implying a compositionalboundary between the two crustal domains. The mantle sourceof the lavas from the Rhenish Massif has higher ²⁰⁶Pb/²⁰⁴Pband ⁸⁷Sr/⁸⁶Sr than the mantle source beneath the Vogelsbergand Hessian Depression. The 30–20 Ma volcanism of theWesterwald apparently had the same mantle source as the QuaternaryEifel lavas, suggesting that the magmas probably formed in apulsing mantle plume with a maximum excess temperature of 100°Cbeneath the Rhenish Massif. The relatively shallow melting ofamphibole-bearing peridotite beneath the Vogelsberg and HessianDepression may indicate an origin from a metasomatized portionof the thermal boundary layer. KEY WORDS: continental rift volcanism; basanites; trachytes; assimilation; fractional crystallization; partial melting     

Tertiary Mafic Lavas of Turkana, Kenya: Constraints on East African Plume Structure and the Occurrence of High-{micro} Volcanism in Africa

The East African Rift System is important to understanding plume-initiatedrifting as manifest in the geochemistry of mafic lavas eruptedalong the rift throughout its evolution. We present new datafrom high-MgO Tertiary lavas from Turkana, northern Kenya, toinvestigate regional melt source components, to identify thedepths and degrees of melting, and to characterize spatiallyand temporally the chemical structure of the underlying mantle.The Turkana area is a region of high lithospheric extensionthat sits between two topographic uplifts thought to be surfaceexpressions of one or more upwelling mantle plumes. Thinningof local crust is believed to be accompanied by widespread removalof the mantle lithosphere, causing the asthenosphere to be inclose contact with the overlying crust. New geochemical dataon basanites, picrites and basalts (MgO >7 wt %) tightlyconstrain the primary melt source regions of Tertiary volcanism.Initial isotopic signatures (¹⁴³Nd/¹⁴⁴Nd = 0·51267–0·51283,⁸⁷Sr/⁸⁶Sr = 0·7031–0·7036) and trace elementabundances (Ce/Pb 30, La/Nb = 0·6–0·8 andBa/Nb = 3–10) in these lavas are consistent with derivationfrom sub-lithospheric sources. Basalts and picrites eruptedbetween 23 and 20 Ma have Sr–Nd–Pb–He isotopiccharacteristics indicative of high-µ influence, recordhigh depths and degrees of partial melting, and are associatedwith rift propagation to the north and south. Accordingly, theselavas sample a source region that is geochemically distinctfrom that reflected both in Oligocene Ethiopian flood basaltsand in the modern Afar region. The geochemical data supportnumerical and theoretical models as well as tomographic resultsproviding for a complex thermal structure in the mantle beneathEast Africa and are interpreted to reflect isotopically distinctplume heads beneath Tanzania and Afar that are derived fromthe chemically heterogeneous South African superplume. KEY WORDS: East African Rift System; mantle plumes; HIMU; geochemistry; Afar     

Source of the Quaternary Alkalic Basalts, Picrites and Basanites of the Potrillo Volcanic Field, New Mexico, USA: Lithosphere or Convecting Mantle?

The <80 ka basalts–basanites of the Potrillo VolcanicField (PVF) form scattered scoria cones, lava flows and maarsadjacent to the New Mexico–Mexico border. MgO ranges upto 12·5%; lavas with MgO < 10·7% have fractionatedboth olivine and clinopyroxene. Cumulate fragments are commonin the lavas, as are subhedral megacrysts of aluminous clinopyroxene(with pleonaste inclusions) and kaersutitic amphibole. REE modellingindicates that these megacrysts could be in equilibrium withthe PVF melts at 1·6–1·7 GPa pressure. Thelavas fall into two geochemical groups: the Main Series (85%of lavas) have major- and trace-element abundances and ratiosclosely resembling those of worldwide ocean-island alkali basaltsand basanites (OIB); the Low-K Series (15%) differ principallyby having relatively low K₂O and Rb contents. Otherwise, theyare chemically indistinguishable from the Main Series lavas.Sr- and Nd-isotopic ratios in the two series are identical andvary by scarcely more than analytical error, averaging ⁸⁷Sr/⁸⁶Sr= 0·70308 (SD = 0·00004) and ¹⁴³Nd/¹⁴⁴Nd = 0·512952(SD=0·000025). Such compositions would be expected ifboth series originated from the same mantle source, with Low-Kmelts generated when amphibole remained in the residuum. ThreePVF lavas have very low Os contents (<14 ppt) and appearto have become contaminated by crustal Os. One Main Series picritehas 209 ppt Os and has a _Os value of +13·6, typical forOIB. This contrasts with published ¹⁸⁷Os/¹⁸⁸Os ratios for KilbourneHole peridotite mantle xenoliths, which give mostly negative_Os values and show that Proterozoic lithospheric mantle formsa thick Mechanical Boundary Layer (MBL) that extends to 70 kmdepth beneath the PVF area. The calculated mean primary magma,in equilibrium with Fo₈₉, has Na₂O and FeO contents that givea lherzolite decompression melting trajectory from 2·8GPa (95 km depth) to 2·2 GPa (70 km depth). Inverse modellingof REE abundances in Main Series Mg-rich lavas is successfulfor a model invoking decompression melting of convecting sub-lithosphericlherzolite mantle (Nd = 6·4; T_p 1400°C) between90 and 70 km. Nevertheless, such a one-stage model cannot accountfor the genesis of the Low-K Series because amphibole wouldnot be stable within convecting mantle at T_f 1400°C. Thesemagmas can only be accommodated by a three-stage model thatenvisages a Thermal Boundary Layer (TBL) freezing conductivelyonto the 70 km base of the Proterozoic MBL during the 20 Myrtectonomagmatic quiescence before PVF eruptions. As it grew,this was veined by hydrous small-fraction melts from below.The geologically recent arrival of hotter-than-ambient (T_p 1400°C) convecting mantle beneath the Potrillo area re-meltedthe TBL and caused the magmatism. KEY WORDS: western USA; picrites; Sr–Nd–Os isotopes; petrogenetic modelling; thermal boundary layer     

Crustal Trace Element and Isotopic Signatures in Garnet Pyroxenites from Garnet Peridotite Massifs from Lower Austria

Gamet-bearing high-temperature peridotite massifs in lower Austriawere exhumed during Carboniferous plate convergence in the Bohemianmassif. The peridotite massifs contain garnet pyroxenite layers,most of which are high-pressure cumulates that crystallizedin the deep lithosphere during ascent and cooling of hot asthenosphericmelts. Many of the pyroxenites have negative Eu anomalies andhigh LREE abundances in pyroxenes and bulk rocks, ⁸⁷Sr/⁸⁶Sr(335 Ma) as high as 0.7089, and Nd (335 Ma) as low as –4.8(leached clinopyroxenes and garnets). These pyroxenites alsoshow strong depletions in Rb, K, Ta, P and Ti compared withthe REE Equilibrium melt compositions calculated from the cumulatecompositions have very high LREE abundances (La_n = 300–600)and show strong LREEfractionation [(La/Sm)_n = 7–47)].Trace element abundances, the Ca–Al-rich composition ofthe cumulates and possible Ti saturation in the melts suggestthat these melts were of primitive carbonatitic–meliliticor lamprophyrt-like composition. Other garnet pyroxenites suchas Al-rich garnet-kyanite clinopyroxemtes with positive Eu anomaliesprobably represent metamorphosed crustal rocks which were subductedand accreted to the lithospheric mantle. The high ⁸⁷Sr/⁸⁶Sr,low Nd (335 Ma) and negative Eu anomalies of the high-pressurecumulates can be explained if their equilibrium melts containeda component derived from subducted upper-crustal rocks. Thehigh equilibration pressures of the host peridotites (3–3.5GPa) and the high equilibration temperatures of the pyroxenites(1100–1400C) indicate that these melts are likely tobe derived from the sub-lithospheric mantle. There, meltingmay have been triggered by small amounts of melt or fluids derivedfrom a subducting slab at greater depth. KEY WORDS: garnet pyroxenites; geochemistry; lower Austria; ultramafic massifs; subduction     

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     

Volcanism in the Vitim Volcanic Field, Siberia: Geochemical Evidence for a Mantle Plume Beneath the Baikal Rift Zone

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/⁸⁶Sr_i(0·7039–0·7049), ¹⁴³Nd/¹⁴⁴Nd_i (0·5127–0·5129)and ¹⁷⁶Hf/¹⁷⁷Hf_i (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     

Upper-Mantle Fragments from Beneath the Sierra Nevada Batholith: Partial Fusion, Fractional Crystallization, and Metasomatism in a Subduction Related Ancient Lithosphere

Upper-mantle xenoliths in volcanic pipes cutting the axis ofthe Sierra Nevada batholith contain predominantly spinel-bearingperidotites (with sporadic garnet) and garnet websterites. Inspite of the enormous thickness of the Sierran crust, the Sierranupper mantle has not attained the garnet peridotite stabilityfield. The peridotites have forsteritic (Fo_88–92) olivines,Cr-diopsides, Cr-spinels, and magnesian orthopyroxenes (En_88–92).Their texture and compositional characteristics of the coexistingphases indicate that these are fragments of the upper mantlethat had undergone various degrees of partial fusion. The Pconditions of reequilibration and mineralogical characteristicssuggest that the partial fusion was accompanied by diapiricuprise. The REE distribution patterns are nearly chondritic.Garnet websterite xenoliths also contain magnesian and Cr-richphases. Their bulk chemical compositions are like pyroxenitecumulates. The garnet websterites from Big Creek differ fromthose occurring at Pick and Shovel in having more Fe-rich phasesand occasional hydrous minerals. The Pick and Shovel garnetwebsterites are interpreted to be pyroxene-rich, garnet-freecumulates formed by fractional crystallization of melts generatedby partial melting of subcontinental lithosphere at depth 60km. The REE abundance of these xenoliths is consistent withthis mode of origin. Presence of jadeitic clinopyroxenes andF-rich phlogopites, and the LREE- and ⁸⁷Sr/⁸⁶Sr-enriched characterof the garnet websterites from Big Creek may suggest their originas metasomatized upper-mantle garnet peridotites. The latestP-T conditions of equilibration of all garnet-bearing samplesshow that they lie along a nearly adiabatic gradient in therange of 900–1000 C and 18–32 kbar. An isotopically heterogeneous, old (1 b.y.) subcontinental lithosphere,characterized by high ⁸⁷Sr/⁸⁶Sr (0.7044–0.7082), radiogenic²⁰⁶Pb/²⁰⁴Pb (18.86–20.04), ²⁰⁷Pb/²⁰⁴Pb (15.64–15.69)and ²⁰⁸Pb/²⁰⁴Pb (38.69–39.11), and moderate ¹⁴³Nd/¹⁴⁴Nd(0.51234–0.51260; E_Nd–0.35 to –5.8) is consideredto be the source of these rocks. There was a fluid influx froma subducted slab carrying Ba, K, Rb, U, Th, and radiogenic Pbinto the overlying ancient lithosphere.     

Petrology and Trace Element Geochemistry of the Honolulu Volcanics, Oahu: Implications for the Oceanic Mantle below Hawaii

The Honolulu Volcanics comprises small volume, late-stage (post-erosional)vents along rifts cutting the older massive Koolau tholeüticshield on Oahu, Hawaii. Most of these lavas and tuff of theHonolulu Volcanics have geochemical features expected of near-primarymagmas derived from a peridotite source containing Fo_87–89olivine; e. g. 100 Mg/(Mg + Fe²⁺) >65, >250 p. p. m. Ni,and presence of ultramafic mantle xenoliths at 18 of the 37vents. Consequently, the geochemistry of the alkali olivinebasalt, basanite, nephelinite and nepheline melilitite lavasand tuff of the Honolulu Volcanics have been used to deducethe composition of their mantle source and the conditions underwhich they were generated by partial melting in the mantle. Compositional trends in 30 samples establish that the magmaswere derived by partial melting of a garnet (<10 per cent)Iherzolite source, which we infer to have been carbon-bearing,from analogy with experimental results. This source was isotopicallyhomogeneous (Sr, Lanphere & Dalrymple, 1980; Pb, Sun, 1980;Nd, Roden et al., 1981), and we infer that the source was compositionallyuniform in all major-element oxides except TiO₂, in compatibletrace elements (Sc, V, Cr, Mn, Co and Ni), and in highly incompatibletrace elements (P, Th, La, Ce). However, the source appearsto have been heterogeneous in TiO₂, Zr, Hf, Nb, and Ta, elementsthat were not strongly incompatible during partial melting.Some nepheline melilitite samples may be derived from a sourcewith distinct Sc and heavy-rare-earth-elements (REE) abundances,or which had a phase or phases controlling the distributionof these elements. The relatively limited abundance range for several elements,such as Ti, Zr, Nb, is partly a consequence of the low degreesof melting inferred for the series (2 per cent for nephelinemelilitite, 11 per cent for alkali olivine basalt), which failedto exhaust the source in minor residual phases. We infer thatthese residual phases probably included phlogopite, amphibole,and another Ti-rich phase (an oxide?), but not apatite. In comparison with estimates of a primordial mantle compositionand the mantle source of mid-oceanic-ridge basalt the garnetperidotite source of the Honolulu Volcanics was increasinglyenriched in the sequence heavy REEs, Y, Tb, Ti, Sm, Zr, andHf all <P <Nd <Sr Ce <La <Nb Ta. A multi-stagehistory for the source of the Honolulu Volcanics is requiredbecause this enrichment was superimposed on a mantle that hadbeen previously depleted in incompatible elements, as indicatedby the relatively low ⁸⁷Sr/⁸⁶Sr ratio, high ¹⁴³Nd/¹⁴⁴Nd ratioand low contents of K, Rb, Ba, and Th. The composition of thesource of the Honolulu Volcanics differs from the source ofthe previously erupted tholeiitic shield. The modal mineralogyof the source of the Honolulu Volcanics is not represented inthe upper-mantle xenoliths, e. g. the garnet pyroxenite andolivine-poor garnet Iherzolite included within the lavas andtuff of the unit.     

Evolution of Calc-alkaline Magmas in Continental Arc Volcanoes: Evidence from Alicudi, Aeolian Arc (Southern Tyrrhenian Sea, Italy)

Major, trace element, and Sr isotopic data are reported forvolcanic rocks from the island of Alicudi, Aeolian Arc, SouthernTyrrhenian Sea. The island is constructed of basalt, basalticandesite to high-K andesite lavas, and pyroclastites, whichshow a continuum in the variation of many major and trace elements.Total iron, MgO, CaO, Ni, Co, Sc, and Cr decrease with increasingsilica, whereas incompatible elements Rb, Ba, Th, and LREE displaythe opposite tendency. Very significant positive correlationsare defined by incompatible elements on interelemental variationdiagrams. Sr isotopic ratios vary from 0–70352 to 0–70410.Overall, basalts (0–70352–O-70410) and basalticandesltes (0–70356–0–70409) are enriched in⁸⁷Sr compared with high-K andesites (O–70352–O–70367),which display the lowest Sr isotopic ratios within the entireAeolian archipelago. Overall negative relationships exist between⁸⁷Sr/⁸⁶Sr and several incompatible trace element abundancesand ratios, such as Th, U, LREE, Zr, La/Yb, and Th/Hf. Otherelemental ratios such as La/Rb, Ba/Rb, and Sr/Rb show more complexbehaviour, even though negative correlations with Sr isotopicratios are observed in the basalts. The observed compositional variations are best explained interms of a model in which primitive calc-alkaline magmas evolvedby crystal-liquid fractionation to give a series of variouslydifferentiated liquids, which underwent different degrees ofinteraction with crustal material. The more mafic and hotterbasaltic liquids appear to have assimilated higher amounts ofmetamorphic wall rocks than did the cooler late erupted andesiticmagmas. This process produced significant variations of Sr isotopicratios, Rb, Cs, Rb/Sr ratios, and LILE/Rb ratios in mafic magmas,but had only minor effects on the abundances and ratios of otherincompatible elements such as Th, LREE, La/Yb, and Th/Hf. When compared with mafic rocks from other Aeolian islands, theAlicudi basalts are more primitive geochemically and isotopically.Going eastward, there is a decrease in Ni and Cr abundances,mg-number and Nd isotopic ratios which parallels an increaseof Sr isotopic ratios in basaltic rocks along the arc. Thesecompositional variations are typical of volcanic series whichhave undergone interaction with upper-crustal material, andsuggest that this process may have contributed significantlyto the regional geochemical and isotopic trends observed inthe Aeolian arc.     

The Mesozoic to Early Cenozoic Magmatism of the Benue Trough (Nigeria); Geochemical Evidence for the Involvement of the St Helena Plume

The Benue Trough is a continental rift related to the openingof the equatorial domain of the South Atlantic which was initiatedin Late Jurassic-Early Cretaceous times. Highly diversifiedand volumetrically restricted Mesozoic to Cenozoic magmaticproducts are scattered throughout the rift. Three periods ofmagmatic activity have been recognized on the basis of ⁴⁰ Ar-³⁹Ar ages: 147–106 Ma, 97–81 Ma and 68–49 Ma.Trace element and Sr, Nd and Pb isotope determinations, performedon selected basaltic samples, allow two groups of basaltic rocksto be identified: (1) a group with a tholeiitic affinity, withZr/Nb=7–11.1; La/Nb = 0.77–1; ⁸⁷Sr/⁸⁶Sr; =0.7042–0.7065¹⁴³Nd/¹⁴⁴Nd;_i = 0.5125–0.5127; ²⁰⁶Pb/²⁰⁴Pb_i = 17.59–18.48;(2) a group with an alkaline affinity, with Zr/Nb = 3.6–6.8;La/Nb=0.53–0.66; ⁸⁷Sr/⁸⁶ Sr_i=0.7029–0.7037; ¹⁴³Nd/¹⁴⁴Nd_i=0.5126–0.5129;²⁰⁶Pb/²⁰⁴Pb_i = 18.54–20.42. The geochemical data leadto the conclusion that three types of mantle sources were involvedin the genesis of the Mesozoic to Cenozoic basaltic rocks ofthe Benue, without significant crustal contamination: (1) anenriched subcontinental lithospheric mantle from which the tholeiiticbasalts were derived; (2) a HIMU-type (plume) component fromwhich the alkaline basalticrocks originated; (3) a depletedasthenospheric mantle (N-MORB-type source), which was involvedin the genesis of the alkaline basaltic magmas. According to(1) the postulated location of the St Helena hot spot in theEquatorial Atlantic at about 130 Ma and (2) the isotopic compositionof the alkaline basaltic rocks of the Benue Trough and theirgeochemical similarity with the basalts of St Helena, we concludethat the St Helena plume was involved in the genesis of thealkaline magmatism of the Benue at the time of opening of theEquatorial Atlantic. Moreover, the geochemical similarity betweenthe alkaline magmatism of the Benue Trough and that of the CameroonLine suggests that both magmatic provinces were related to theSt Helena plume. Finally, the temporal change of the mantlesources observed in the Benue Trough can be accounted for bythe recent models of plume dynamics, in the general frameworkof opening of the Equatorial Atlantic. KEY WORDS: Benue Trough; Mesozoic to Cenozoic magmatism; Equatorial Atlantic; mantle sources; St Helena plume ^*;Corresponding author.     

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     

Archean Shoshonitic Lamprophyres of the Abitibi Subprovince, Canada: Petrogenesis, Age, and Tectonic Setting

Archean shoshonitic lamprophyre dikes are prevalent along majortranslithospheric structures that demark tectonostratigraphicterranes in the Abitibi greenstone belt of the Superior Province.The lamprophyres post-date volcanism, tonalitic batholiths,deformation, and metamorphism of the terranes, and are mostprominently developed in trans-tensional graben, where theyare associated with molasse sediments and an alkaline suiteof plutons, stocks, and trachytes. Mineralogically, the dikesare characterized by zoned phiogopite or hornblende phenocrystsand/or diopsidic pyroxene, restriction of feldspar to the groundmass,globular segregations of K-feldspar and calcite, olivine ‘pilite’,and accessory Ti-magnetite, Cr-spinel, apatite, titanite, andSr-rich calcite; crustal xenoliths are sporadically present. Compositionally, weakly altered primititive dikes have contentsof SiO₂ (41–48 wt.%), TiO₂ (06–11 wt.%), P₂O₅(041–076 wt.%), Cr (258–915 ppm), Co (36–84ppm), Ni (159–368 ppm), and Sc (15–32 ppm), mg-numbers(72–79), and K₂O/Na₂O ratios (10–43) similar tothose of Phanerozoic shoshonitic lamprophyres. The primitivedikes are also characterized by extreme enrichments of K, Rb,Ba, Cs, U, and Th, enhanced light rare earth elements (REE),and fractionated REE patterns [La_n=33–274; (La/Yb)_n=16–87].On mid-ocean ridge basalt (MORB) normalized plots the dikesshow coherent patterns, with (1)enrichment of K, Rb, and Barelative to Sr and LREE, (2) variable enrichments of Rb andBa relative to K, (3) troughs at Ta–Nb and Ti, and (4)variable negative P and positive Sm anomalies. Compositionalvariations of lamprophyre suites within restricted areas areinterpreted to reflect melting of compositionally heterogeneoussources, variable degrees of assimilation–fractional crystallization,and mixing of distinct batches of lamprophyric magmas. Primary¹⁸O values of the magmas are close to 63 as given by resistantpyroxene; these are ¹⁸O-relative to MORB, but comparable withPhanerozoic alkali basalts and lamprophyres. Mica, clinopyroxene,hornblende, and feldspar do not retain magmatic equilibriumfractionations for oxygen isotopes. A concordant U–Pbage of 26742 Ma was obtained from titanite, similar to theages of shoshonitic plutons in the same area. The lamprophyredikes possess a total range of _Nd between 041 and 211(1),and define a distinct field in common with other late Archeanshoshonites on an f^(Sm/Nd) vs. _Nd plot. Pyroxenes yield a low⁸⁷Sr/⁸⁶Sr(0701102), whereas whole-rock Rb-Sr isotope systematicsare disturbed. Lamprophyres are not known from pre-27-Ga terranes. Their compositionand inferred geodynamic setting is consistent with an originin a depleted mantle wedge, enriched in large ion lithophileelements (LILE) and LREE during subduction by slab and sediment(low Sr/Nd) dehydration. Partial melting may have been triggeredby rebound and decompression that followed accretional collisionof two allochthonous greenstone terranes at a plate margin.The onset of shoshonitic magmatism at 27 Ga coincides withthe transition from tonalite–trondhjemite–granodiorite(TTG) dominated magmatism with high (La/Yb)_n and low Yb (slabmelting) to mantle-wedge derived granites featuring lower (La/Yb)_nand higher Yb (slab dehydration), owing to decreasing heat flow.Accretion of greenstone belts, and their buoyant harzburgiticroots, consolidated a thick subcontinental mantle lithosphereby 27 Ga, which was subsequently the source of Jurassic kimberlitesthat intruded the persistently reactivated Archean translithosphericstructures.     

Sr-Nd-Pb Isotopic Compositions of Peridotite Xenoliths from Spitsbergen: Numerical Modelling Indicates Sr-Nd Decoupling in the Mantle by Melt Percolation Metasomatism

Several spinel peridotite xenoliths from Spitsbergen have Sr–Ndisotopic compositions that plot to the right of the ‘mantlearray’ defined by oceanic basalts and the DM end-member(depleted mantle, with low ⁸⁷Sr/⁸⁶Sr and high ¹⁴³Nd/¹⁴⁴Nd).These xenoliths also show strong fractionation of elements withsimilar compatibility (e.g. high La/Ce), which cannot be producedby simple mixing of light rare earth element-depleted peridotiteswith ocean island basalt-type or other enriched mantle melts.Numerical simulations of porous melt flow in spinel peridotitesapplied to Sr–Nd isotope compositions indicate that thesefeatures of the Spitsbergen peridotites can be explained bychemical fractionation during metasomatism in the mantle. ‘Chromatographic’effects of melt percolation create a transient zone where thehost depleted peridotites have experienced enrichment in Sr(with a radiogenic isotope composition) but not in Nd, thusproducing Sr–Nd decoupling mainly controlled by partitioncoefficients and abundances of Sr and Nd in the melt and theperidotite. Therefore, Sr–Nd isotope decoupling, earlierreported for some other mantle peridotites worldwide, may bea signature of metasomatic processes rather than a source-relatedcharacteristic, contrary to models that invoke mixing with hypotheticalSr-rich fluids derived from subducted oceanic lithosphere. Pbisotope compositions of the Spitsbergen xenoliths do not appearto be consistently affected by the metasomatism. KEY WORDS: Spitsbergen; lithospheric mantle; metasomatism; radiogenic isotopes; theoretical modelling