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     

Spatial and temporal geochemical variability in lacustrine sedimentation in the East African Rift System: Evidence from the Kenya Rift and regional analyses

Many previous studies on lacustrine basins in the East African Rift System have directed their attention to climatic controls on contemporary sedimentation or climate change as part of palaeoenvironmental reconstruction. In contrast, this research focuses on the impact of tectonism and volcanism on rift deposition and develops models that help to explain their roles and relative importance. The study focuses on the spatial and temporal variability in bulk sediment geochemistry from a diverse range of modern and ancient rift sediments through an analysis of 519 samples and 50 major and trace elements. The basins examined variously include, or have contained, wetlands and/or shallow to deep, fresh to hypersaline lakes. Substantial spatial variability is documented for Holocene to modern deposits in lakes Turkana, Baringo, Bogoria, Magadi and Malawi. Mio‐Pleistocene sediments in the Central Kenya Rift and Quaternary deposits of the southern Kenya Rift illustrate temporal variability. Tectonic and volcanic controls on geochemical variability are explained in terms of: (i) primary controlling factors (faulting, subsidence, uplift, volcanism, magma evolution and antecedent lithologies and landscapes); (ii) secondary controls (bedrock types, rift shoulder and axis elevations, accommodation space, meteoric and hydrothermal fluids and mantle CO ₂); and (iii) response factors (catchment area size, orographic rains, rain shadows, vegetation densities, erosion and weathering rates, and spring/runoff ratios). The models developed have, in turn, important implications for palaeoenvironmental interpretation in other depositional basins.     

Isotope Compositions of Submarine Hana Ridge Lavas, Haleakala Volcano, Hawaii: Implications for Source Compositions, Melting Process and the Structure of the Hawaiian Plume

We report Sr, Nd, and Pb isotope compositions for 17 bulk-rocksamples from the submarine Hana Ridge, Haleakala volcano, Hawaii,collected by three dives by ROV Kaiko during a joint Japan–USHawaiian cruise in 2001. The Sr, Nd, and Pb isotope ratios forthe submarine Hana Ridge lavas are similar to those of Kilauealavas. This contrasts with the isotope ratios from the subaerialHonomanu lavas of the Haleakala shield, which are similar toMauna Loa lavas or intermediate between the Kilauea and MaunaLoa fields. The observation that both the Kea and Loa componentscoexist in individual shields is inconsistent with the interpretationthat the location of volcanoes within the Hawaiian chain controlsthe geographical distribution of the Loa and Kea trend geochemicalcharacteristics. Isotopic and trace element ratios in Haleakalashield lavas suggest that a recycled oceanic crustal gabbroiccomponent is present in the mantle source. The geochemical characteristicsof the lavas combined with petrological modeling calculationsusing trace element inversion and pMELTS suggest that the meltingdepth progressively decreases in the mantle source during shieldgrowth, and that the proportion of the recycled oceanic gabbroiccomponent sampled by the melt is higher in the later stagesof Hawaiian shields as the volcanoes migrate away from the centralaxis of the plume. KEY WORDS: submarine Hana Ridge; isotope composition; melting depth; Hawaiian mantle plume     

Mafic Pegmatites Intruding Oceanic Plateau Gabbros and Ultramafic Cumulates from Bolivar, Colombia: Evidence for a 'Wet' Mantle Plume?

The fault-bounded Bolívar Ultramafic Complex (BUC) onthe eastern fringes of the Western Cordillera of Colombia wastectonically accreted onto the western coast of South Americain the late Cretaceous–early Tertiary, along with pillowbasalts of the Caribbean–Colombian Oceanic Plateau (CCOP).The complex consists of a lower sequence of ultramafic cumulates,successively overlain by layered and isotropic gabbroic rocks.The gabbros grade into, and are intruded by, mafic pegmatitesthat consist of large magnesiohornblende and plagioclase crystals.These pegmatites yield a weighted mean ⁴⁰Ar–³⁹Ar step-heatingage of 90·5 ± 0·9 Ma and thus coincidewith the timing of peak CCOP volcanism. The chemistry of theBUC is not consistent with a subduction-related origin. However,the similarity in Sr–Nd–Pb–Hf isotopes betweenthe CCOP and the BUC, in conjunction with their indistinguishableages, suggests that the BUC is an integral part of the plume-derivedCCOP. The parental magmas of the Bolívar complex wereprobably hydrous picrites that underwent 20–30% crystallization.The residual magmas from this fractionation contained     

Erosion of lithospheric mantle beneath the East African Rift system: geochemical evidence from the Kivu volcanic province

This study presents new major and trace element and Sr–Nd isotopic results for a suite of Miocene–Recent mafic lavas from the Kivu volcanic province in the western branch of the East African Rift. These lavas exhibit a very wide range in chemical and isotopic characteristics, due to a lithospheric mantle source region that is heterogeneous on a small scale, probably <1 km. The chemical and isotopic variations are mostly geographically controlled: lavas from Tshibinda volcano, which lies on a rift border fault on the northwestern margin of the province, have higher values of ⁸⁷Sr/⁸⁶Sr, (La/Sm)_n, Ba/Nb, and Zr/Hf than the majority of Kivu (Bukavu) samples. The range of ⁸⁷Sr/⁸⁶Sr at Tshibinda (0.70511–0.70514) overlaps some compositions found in the neighboring Virunga province, while Bukavu group lavas include the lowest ⁸⁷Sr/⁸⁶Sr (0.70314) and highest _Nd (+7.6) yet measured in western rift lavas. The Tshibinda compositions trend towards a convergence for Sr–Nd–Pb isotopic values among western rift lavas. Among Kivu lavas, variations in ¹⁴³Nd/¹⁴⁴Nd correlate with those for certain incompatible trace element ratios (e.g., Th/Nb, Zr/Hf, La/Nb, Ba/Rb), with Tshibinda samples defining one compositional extreme. There are covariations of isotopic and trace element ratios in mafic lavas of the East African Rift system that vary systematically with geographic location. The lavas represent a magmatic sampling of variations in the underlying continental lithospheric mantle, and it appears that a common lithospheric mantle (CLM) source is present beneath much of the East African Rift system. This source contains minor amphibole and phlogopite, probably due to widespread metasomatic events between 500 and 1000 Ma. Lava suites which do not show a strong component of the CLM source, and for which the chemical constraints also suggest the shallowest magma formation depths, are the Bukavu group lavas from Kivu and basanites from Huri Hills, Kenya. The inferred extent of lithospheric erosion therefore appears to be significant only beneath these two areas, which is generally consistent with lithospheric thickness variations estimated from gravity and seismic studies.     

Petrology and Geochemistry of Early Cretaceous Bimodal Continental Flood Volcanism of the NW Etendeka, Namibia. Part 1: Introduction, Mafic Lavas and Re-evaluation of Mantle Source Components

The bimodal NW Etendeka province is located at the continentalend of the Tristan plume trace in coastal Namibia. It comprisesa high-Ti (Khumib type) and three low-Ti basalt (Tafelberg,Kuidas and Esmeralda types) suites, with, at stratigraphicallyhigher level, interstratified high-Ti latites (three units)and quartz latites (five units), and one low-Ti quartz latite.Khumib basalts are enriched in high field strength elementsand light rare earth elements relative to low-Ti types and exhibittrace element affinities with Tristan da Cunha lavas. The unradiogenic²⁰⁶Pb/²⁰⁴Pb ratios of Khumib basalts are distinctive, most plottingto the left of the 132 Ma Geochron, together with elevated ²⁰⁷Pb/²⁰⁴Pbratios, and Sr–Nd isotopic compositions plotting in thelower ¹⁴³Nd/¹⁴⁴Nd part of mantle array (EM1-like). The low-Tibasalts have less coherent trace element patterns and variable,radiogenic initial Sr (     

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     

Petrogenesis of Mafic Inclusions in Rhyolitic Lavas from Narugo Volcano, Northeastern Japan

Mafic inclusions present in the rhyolitic lavas of Narugo volcano,Japan, are vesiculated andesites with diktytaxitic texturesmainly composed of quenched acicular plagioclase, pyroxenes,and interstitial glass. When the mafic magma was incorporatedinto the silica-rich host magma, the cores of pyroxenes andplagioclase began to crystallize (>1000°C) in a boundarylayer between the mafic and felsic magmas. Phenocryst rim compositionsand interstitial glass compositions (average 78 wt % SiO₂) inthe mafic inclusions are the same as those of the phenocrystsand groundmass glass in the host rhyolite. This suggests thatthe host felsic melt infiltrated into the incompletely solidifiedmafic inclusion, and that the interstitial melt compositionin the inclusions became close to that of the host melt (c.850°C). Infiltration was enhanced by the vesiculation ofthe mafic magma. Finally, hybridized and density-reduced portionsof the mafic magma floated up from the boundary layer into thehost rhyolite. We conclude that the ascent of mafic magma triggeredthe eruption of the host rhyolitic magma. KEY WORDS: mafic inclusion; stratified magma chamber; magma mixing; mingling; Narugo volcano; Japan     

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     

Flood and Shield Basalts from Ethiopia: Magmas from the African Superswell

The Ethiopian plateau is made up of several distinct volcaniccentres of different ages and magmatic affinities. In the NE,a thick sequence of 30 Ma flood basalts is overlain by the 30Ma Simien shield volcano. The flood basalts and most of thisshield volcano, except for a thin veneer of alkali basalt, aretholeiitic. In the centre of the province, a far thinner sequenceof flood basalt is overlain by the 22 Ma Choke and Guguftu shieldvolcanoes. Like the underlying flood basalts, these shieldsare composed of alkaline lavas. A third type of magma, whichalso erupted at 30 Ma, is more magnesian, alkaline and stronglyenriched in incompatible trace elements. Eruption of this magmawas confined to the NE of the province, a region where the lavaflows are steeply tilted as a result of deformation contemporaneouswith their emplacement. Younger shields (e.g. Mt Guna, 10·7Ma) are composed of Si-undersaturated lavas. The three maintypes of magma have very different major and trace element characteristicsranging from compositions low in incompatible elements in thetholeiites [e.g. 10 ppm La at 7 wt % MgO (=La₇), La/Yb = 4·2],moderate in the alkali basalts (La₇ = 24, La/Yb = 9·2),and very high in the magnesian alkaline magmas (La₇ = 43, La/Yb= 17). Although their Nd and Sr isotope compositions are similar,Pb isotopic compositions vary considerably; ²⁰⁶Pb/²⁰⁴Pb variesin the range of     

Distinguishing Melting of Heterogeneous Mantle Sources from Crustal Contamination: Insights from Sr Isotopes at the Phenocryst Scale, Pisgah Crater, California

Compositionally heterogeneous basaltic centers from a varietyof tectonic environments, including Pisgah Crater in the MojaveDesert region of California, exhibit secular changes in theirchemistry that might be explained by the sequential meltingof ultramafic to mafic mantle sources. We have analyzed phenocrystsfrom alkali basalts and hawaiites erupted at Pisgah Crater toinvestigate the effects of open-system modifications imposedon basaltic systems. We present ⁸⁷Sr/⁸⁶Sr data for individualphenocrysts of amphibole and clinopyroxene and the first publishedresults of single olivine grains, in addition to plagioclase.Each mineral phase exhibits a range in Sr isotope compositionthat may only partially overlap the isotopic composition ofthe other mineral phases, suggesting an interplay between twomagmatic end-members that continued up to the time of eruption.Limited ⁸⁷Sr/⁸⁶Sr variability in minerals from early and intermediatelavas indicates only moderate syn-crystallization open-systemmodification, whereas minerals in late-erupted lavas have muchhigher ⁸⁷Sr/⁸⁶Sr, consistent with extensive open-system modification.Rimward increases in ⁸⁷Sr/⁸⁶Sr of plagioclase confirm that thesechanges occurred within the stability field of plagioclase and,therefore, at crustal or near-crustal depths. The major elementcompositions of olivine-hosted melt inclusions indicate thatan Al-rich component of andesitic composition (⁸⁷Sr/⁸⁶Sr 0·7056),possibly derived from plagioclase-rich cumulates or pelites,was assimilated by magma generated from asthenosphere or younglithosphere with ⁸⁷Sr/⁸⁶Sr 0·7038. The results clearlydemonstrate the utility of measuring the ⁸⁷Sr/⁸⁶Sr of individualminerals and indicate that Pisgah Crater basalts probably acquiredisotopically enriched geochemical signatures from crustal contamination,rather than from mixing of heterogeneous mantle melts. KEY WORDS: assimilation; basalts; melt inclusions; minerals; Sr isotopes     

Rates and Timescales of Fractional Crystallization from 238U-230Th-226Ra Disequilibria in Trachyte Lavas from Longonot Volcano, Kenya

A suite of peralkaline trachytes from Longonot volcano, Kenya,which erupted during the last 6000 years, has been analysedfor major and trace elements, Pb and Nd isotopes, and U–Th–Radisequilibria. The lavas are divided into three stratigraphicgroups of trachytes (Lt²a, Lt²b and Lt³), and hybrid lavas,designated LMx¹ and LMx², which, respectively, pre-date andpost-date the Lt² lavas. Major and trace elements are consistent,with up to 37% within-group fractional crystallization of predominantlyalkali feldspar. The parental magma for the different trachytegroups had a more mafic composition—probably hawaiitic.Nd and Pb isotopes show minimal variation, both within and betweenmagma groups, and indicate that up to 10% comendite magma fromthe neighbouring Olkaria volcanic field may have intermixedwith the Longonot magma. (²³⁰Th/²³⁸U) disequilibria indicatethat limited U/Th fractionation occurred during the past 10kyr, whereas (²²⁶Ra/²³⁰Th) disequilibria reflect the effectof alkali feldspar fractionation >8 kyr ago in the Lt²a lavas,between 3 and 7 kyr ago in the Lt²b lavas and in the past 3kyr for the Lt³ lavas. (²²⁶Ra/²³⁰Th) disequilibria in the Lt²blavas are interpreted using a model that combines the equationsof radioactive decay and in-growth with Rayleigh crystallizationto give fractionation rates of about 0·2 x 10^–4/yearfor the evolution of hawaiite to trachyte, but more rapid ratesof up to 3 x 10^–4/year for fractionation within the trachytesequence. (²²⁶Ra/²³⁰Th) from two whole-rock–alkali feldsparpairs are interpreted to show the crystals formed at 5800 yearsBP (Lt²b) and 2800 years BP (Lt³), implying that phenocrystformation continued almost up to the time of eruption. The resultsstrongly indicate that fractionated magmas can be stored forperiods on the order of 1000–2500 years prior to eruption,whereas other magmas were erupted as fractionation was proceeding. KEY WORDS: trachyte; magma chambers; u-series; Kenya     

Geochemistry of South African On- and Off-craton, Group I and Group II Kimberlites: Petrogenesis and Source Region Evolution

Bulk-rock geochemical compositions of hypabyssal kimberlites,emplaced through the Archaean Kaapvaal craton and ProterozoicNamaqua–Natal belt, are used to estimate close-to-primarymagma compositions of Group I kimberlites (Mg-number = 0·82–0·87;22–28 wt % MgO; 21–30 wt % SiO₂; 10–17 wt% CaO; 0·2–1·7 wt % K₂O) and Group II kimberlites(Mg-number = 0·86–0·89; 23–29 wt %MgO; 28–36 wt % SiO₂; 8–13 wt % CaO; 1·6–4·6wt % K₂O). Group I kimberlites are distinguished from GroupII by their lower Ba/Nb (<12), Th/Nb (<1·1) andLa/Nb (<1·1) but higher Ce/Pb (>22) ratios. Thedistinct rare earth element patterns of the two types of kimberlitesindicate a more highly metasomatized source for Group II kimberlites,with more residual clinopyroxene and less residual garnet. Thesimilarity of Sr and Nd isotope ratios and diagnostic traceelement ratios (Ce/Pb, Nb/U, La/Nb, Ba/Nb, Th/Nb) of Group Ikimberlites to ocean island basalts (OIB), but more refractoryMg-numbers and Ni contents, are consistent with derivation ofGroup I kimberlites from subcontinental lithospheric mantle(SCLM) that has been enriched by OIB-like melts or fluids. Sourceenrichment ages and plate reconstructions support a direct associationof these melts or fluids with Mesozoic upwelling beneath southernAfrica of a mantle plume(s), at present located beneath thesouthern South Atlantic Ocean. In contrast, the geochemicalcharacteristics of both on- and off-craton Group II kimberlitesshow strong similarity to calc-alkaline magmas, particularlyin their Nb and Ta depletion and Pb enrichment. It is suggestedthat Group II kimberlites are derived from both Archaean andProterozoic lithospheric mantle source regions metasomatizedby melts or fluids associated with ancient subduction events,unrelated to mantle plume upwelling. The upwelling of mantleplumes beneath southern Africa during the Mesozoic, at the timeof Gondwana break-up, may have acted as a heat source for partialmelting of the SCLM and the generation of both Group I and GroupII kimberlite magmas. KEY WORDS: kimberlite; geochemistry; petrogenesis; mantle plumes; South Africa     

Petrogenesis of Tertiary Mafic Alkaline Magmas in the Hocheifel, Germany

Primitive nephelinites and basanites from the Tertiary Hocheifelarea of Germany (part of the Central European Volcanic Province;CEVP) have high Mg-number (>0·64), high Cr and Nicontents and strong light rare earth element enrichment butsystematic depletion in Rb, K and Ba relative to trace elementsof similar compatibility in anhydrous mantle. Alkali basaltsand more differentiated magmatic rocks have lower Mg-numberand lower abundances of Ni and Cr, and have undergone fractionationof mainly olivine, clinopyroxene, Fe–Ti oxide, amphiboleand plagioclase. Some nephelinites and basanites approach theSr–Nd–Pb isotope compositions inferred for the EAR(European Asthenospheric Reservoir) component. The Nd–Sr–Pbisotope composition of the differentiated rocks indicates thatassimilation of lower crustal material has modified the compositionof the primary mantle-derived magmas. Rare earth element meltingmodels can explain the petrogenesis of the most primitive maficmagmatic rocks in terms of mixing of melt fractions from anamphibole-bearing garnet peridotite source with melt fractionsfrom an amphibole-bearing spinel peridotite source, both sourcescontaining residual amphibole. It is inferred that amphibolewas precipitated in the asthenospheric mantle beneath the Hocheifel,close to the garnet peridotite–spinel peridotite boundary,by metasomatic fluids or melts from a rising mantle diapir orplume. Melt generation with amphibole present suggests relativelylow mantle potential temperatures (<1200°C); thus themantle plume is not thermally anomalous. A comparison of recentlypublished Ar/Ar ages for Hocheifel basanites with the geochemicaland isotopic composition of samples from this study collectedat the same sample sites indicates that eruption of earlierlavas with an EM signature was followed by the eruption of laterlavas derived from a source with EAR or HIMU characteristics,suggesting a contribution from the advancing plume. Thus, theHocheifel area represents an analogue for magmatism during continentalrift initiation, during which interaction of a mantle plumewith the overlying lithosphere may have led to the generationof partial melts from both the lower lithosphere and the asthenosphere. KEY WORDS: alkali basalts; continental volcanism; crustal contamination; partial melting; Eifel, Germany     

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     

Wolf Volcano, Galapagos Archipelago: Melting and Magmatic Evolution at the Margins of a Mantle Plume

Wolf volcano, an active shield volcano on northern Isabela Islandin the Galápagos Archipelago, has undergone two majorstages of caldera collapse, with a phase of partial calderarefilling between. Wolf is a typical Galápagos shieldvolcano, with circumferential vents on the steep upper carapaceand radial vents distributed in diffuse rift zones on the shallower-slopinglower flanks. The radial fissures continue into the submarineenvironment, where they form more tightly focused rift zones.Wolf's magmas are strikingly monotonous: estimated eruptivetemperatures of the majority of lavas span a total of only 22°C.This homogeneity is attributed to buffering of magmas as theyascend through a thick column of olivine gabbroic mush thathas been deposited from a thin, shallow (<2 km deep) subcalderasill that is in a thermochemical steady state. Wolf's lavashave the most depleted isotopic compositions of any historicallyactive intraplate ocean island volcano on the planet and haveisotopic compositions (except for ³He/⁴He) indistinguishablefrom mid-ocean ridge basalt erupted from the GalápagosSpreading Center (GSC) 250–410 km away from the peak ofinfluence of the Galápagos plume. Wolf's lavas are enrichedin incompatible trace elements and have systematic major elementdifferences relative to GSC lavas, however. Wolf's magmas resultfrom lower extents of melting, deeper melt extraction, and agreater influence of garnet compared with GSC magmas, but Wolfand the GSC share the same sources. These melt generation conditionsare attributed to melting in a thermal and mechanical boundarylayer of depleted asthenosphere at the margins of the Galápagosplume. The lower degrees of melting and extraction from deeperlevels result from a thicker lithospheric cap at Wolf than existsat the GSC. KEY WORDS: caldera; Galápagos; mush; partial melting; plume     

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     

The Geochemistry of Ultramafic to Mafic Volcanics from the Belingwe Greenstone Belt, Zimbabwe: Magmatism in an Archean Continental Large Igneous Province

The evolution of the late Archean Belingwe greenstone belt,Zimbabwe, is discussed in relation to the geochemistry of theultramafic to mafic volcanic rocks. Four volcanic types (komatiite,komatiitic basalt, D-basalt and E-basalt) are distinguishedin the 2·7 Ga Ngezi volcanic sequence using a combinationof petrography and geochemistry. The komatiites and D-basaltsare rocks in which isotopic systems and trace elements are depleted.Chemical variations in komatiites and D-basalts can be explainedby fractional crystallization from the parental komatiite. Incontrast, komatiitic basalts and E-basalts are siliceous anddisplay enriched isotopic and trace element compositions. Theirchemical trends are best explained by assimilation with fractionalcrystallization (AFC) from the primary komatiite. AFC calculationsindicate that the komatiitic basalts and E-basalts are derivedfrom komatiites contaminated with 20% and 30% crustal material,respectively. The volcanic stratigraphy of the Ngezi sequence,which is based on field relationships and the trace elementcompositions of relict clinopyroxenes, shows that the leastcontaminated komatiite lies between highly contaminated komatiiticbasalt flows, and has limited exposure near the base of thesuccession. Above these flows, D- and E-basalts alternate. Thekomatiite appears to have erupted on the surface only in theearly stages, when plume activity was high. As activity decreasedwith time, komatiite magmas may have stagnated to form magmachambers within the continental crust. Subsequent komatiiticmagmas underwent fractional crystallization and were contaminatedwith crust to form D-basalts or E-basalts. KEY WORDS: komatiite; crustal assimilation; Belingwe greenstone belt; continental flood basalt; plume magmatism     

Evolution of the Lithospheric Mantle beneath the Marsabit Volcanic Field (Northern Kenya): Constraints from Textural, P-T and Geochemical Studies on Xenoliths

Xenoliths hosted by Quaternary basanites and alkali basaltsfrom Marsabit (northern Kenya) represent fragments of Proterozoiclithospheric mantle thinned and chemically modified during riftingin the Mesozoic (Anza Graben) and in the Tertiary–Quaternary(Kenya rift). Four types of peridotite xenoliths were investigatedto constrain the thermal and chemical evolution of the lithosphericmantle. Group I, III and IV peridotites provide evidence ofa cold, highly deformed and heterogeneous upper mantle. Textures,thermobarometry and trace element characteristics of mineralsindicate that low temperatures in the spinel stability field(750–800°C at <1·5 GPa) were attained bydecompression and cooling from initially high pressures andtemperatures in the garnet stability field (970–1080°Cat 2·3–2·9 GPa). Cooling, decompressionand penetrative deformation are consistent with lithosphericthinning, probably related to the development of the Mesozoicto Paleogene Anza Graben. Re-equilibrated and recrystallizedperidotite xenoliths (Group II) record heating (from 800°Cto 1100°C). Mineral trace element signatures indicate enrichmentby mafic silicate melts, parental to the Quaternary host basanitesand alkali basalts. Relationships between mineral textures,P–T conditions of equilibration, and geochemistry canbe explained by metasomatism and heating of the lithosphererelated to the formation of the Kenya rift, above a zone ofhot upwelling mantle. KEY WORDS: East African Rift System; Anza Graben; in situ LA-ICPMS; peridotite xenoliths; thermobarometry     

The Petrology and Geochemistry of Volcanic Rocks on Jeju Island: Plume Magmatism along the Asian Continental Margin

The incompatible element signatures of volcanic rocks formingJeju Island, located at the eastern margin of the Asian continent,are identical to those of typical intraplate magmas. The sourceof these volcanic rocks may be a mantle plume, located immediatelybehind the SW Japan arc. Jeju plume magmas can be divided intothree series, based on major and trace element abundances: high-aluminaalkalic, low-alumina alkalic, and sub-alkalic. Mass-balancecalculations indicate that the compositional variations withineach magma series are largely governed by fractional crystallizationof three chemically distinct parental magmas. The compositionsof primary magmas for these series, using inferred residualmantle olivine compositions, suggest that the low-alumina alkalicand sub-alkalic magmas are generated at the deepest and shallowestdepths by lowest and highest degrees of melting, respectively.These estimates, together with systematic differences in traceelement and isotopic compositions, indicate that the upper mantlebeneath Jeju Island is characterized by an increased degreeof metasomatism and a change in major metasomatic hydrous mineralsfrom amphibole to phlogopite with decreasing depth. The originalplume material, having rather depleted geochemical characteristics,entrained shallower metasomatized uppermost mantle material,and segregated least-enriched low-alumina alkalic, moderatelyenriched high-alumina alkalic, and highly enriched sub-alkalicmagmas, with decreasing depth. KEY WORDS: Jeju Island; magma genesis; mantle plume; subcontinental mantle