Magma Genesis and Mantle Dynamics at the Harrat Ash Shamah Volcanic Field (Southern Syria)

A geochemical and petrological study of Miocene to recent alkalibasalts, basanites, hawaiites, mugearites, trachytes, and phonoliteserupted within the Harrat Ash Shamah volcanic field was performedto reconstruct the magmatic evolution of southern Syria. Themajor element composition of the investigated lavas is mainlycontrolled by fractional crystallization of olivine, clinopyroxene,± Fe–Ti oxides and ± apatite; feldspar fractionationis restricted to the most evolved lavas. Na₂O and SiO₂ variationswithin uncontaminated, primitive lavas as well as variably fractionatedheavy rare earth element ratios suggest a formation by variabledegrees of partial melting of different garnet peridotite sourcestriggered, probably, by changes in mantle temperature. The isotopicrange as well as the variable trace element enrichment observedin the lavas imply derivation from both a volatile- and incompatibleelement-enriched asthenosphere and from a plume component. Inaddition, some lavas have been affected by crustal contamination.This effect is most prominent in evolved lavas older than 3·5Ma, which assimilated 30–40% of crustal material. In general,the periodicity of volcanism in conjunction with temporal changesin lava composition and melting regime suggest that the Syrianvolcanism was triggered by a pulsing mantle plume located underneathnorthwestern Arabia. KEY WORDS: ⁴⁰Ar/³⁹Ar ages; intraplate volcanism; mantle plume; partial melting; Syria     

Petrogenesis of Volcanic Rocks from Saipan and Rota, Mariana Islands, and Implications for the Evolution of Nascent Island Arcs

An ⁴⁰Ar/³⁹Ar age of 45·1 Ma determined for lavas fromnorthern Saipan confirms that these high-silica rhyolites eruptedduring the ‘proto-arc’ stage of volcanism in theIzu–Bonin–Mariana system, which is characterizedelsewhere by eruption of boninitic lavas. Incompatible traceelement concentrations and Sr, Hf, Nd, and Pb isotope ratiosfor these rhyolites are transitional between those of c. 48Ma boninitic lavas and post-38 Ma ‘first-arc’ andesitesand dacites from Saipan and Rota that have typical subduction-relatedcompositions. These transitional compositions are modeled bycrystal fractionation of parental tholeiitic basalt combinedwith assimilation of young boninitic crust. A second stage ofRayleigh fractionation in the upper crust is required by SiO₂concentrations that exceed 77 wt % and near-zero compatibleelement concentrations. First-arc magma compositions are consistentwith fractionation of basalt and assimilation of crust similarin composition to the first-arc magmas themselves. The mantlesources of the proto-arc and first-arc lavas from Saipan andRota are similar to those of Philippine back-arc basin basaltsbased on Nd and Hf isotopic compositions. The Pb isotope compositionsof these lavas are between those of Pacific sea-floor basaltsand Jurassic and younger cherty and clay-rich sediments. Thiscontrasts with the boninitic proto-arc volcanic rocks from Guamand Deep Sea Drilling Project Sites 458 and 459 that have Pbisotope compositions similar to Pacific basin basalts and volcaniclasticsediments. The preferred explanation for the difference in thenature of proto-arc volcanism between Saipan and other fore-arclocations is that the crust ceased extending 3–4 Myr earlierbeneath Saipan. This was caused by a change from mantle upwelling,fore-arc extension, and shallow melting to an environment dominatedby more normal mantle wedge convection, stable crust, and deepermelting. KEY WORDS: rhyolite; andesite; Mariana arc; isotope ratios; trace elements     

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     

Geochemistry of the Active Azufre--Planchon--Peteroa Volcanic Complex, Chile (3515'S): Evidence for Multiple Sources and Processes in a Cordilleran Arc Magmatic System

Along strike of the Quaternary magmatic arc in the SouthernVolcanic Zone of the Andes, there is a south to north increasein crustal thickness, and the lavas define systematic geochemicaltrends which have been attributed to variations in the proportionsand compositions of mantle-and crustal-derived components. Realisticinterpretations of these regional geochemical trends requiresan understanding of the sources and processes that control lavacompositions at individual volcanoes. Because it is in an importantgeophysical and geochemical transition zone, we studied theAzufre—Planchon—Peteroa volcanic complex, a nestedgroup of three volcanoes <055 m.y. in age located at 3515'Sin the Southern Volcanic Zone of the Andes. North of this complexat 33–35S the continental crust is thick, basalts areabsent, and there is abundant evidence for crustal componentsin the evolved lavas, but south of 37S, where the crust isrelatively thin, basaltic lavas are abundant and the contributionof continental crust to the lavas is less obvious. In additionto its location, this volcanic complex is important becausethere is a diversity of lava compositions, and it is the northernmostexposure of recent basaltic volcanism on the volcanic front.Therefore, the lavas of this complex can be used to identifythe relative roles of mantle, lower-crustal and upper-crustalsources and processes at a single location. Volcan Azufre is the oldest and largest volcano of the complex;it is a multi-cycle, bimodal, basaltic andesite–dacitestratovolcano. Volcan Planchon is the northernmost basalt-bearingvolcano along the volcanic front of the Southern Andes, andVolcan Peteroa, the youngest volcano of the complex, has eruptedmixed magmas of andesitic and dacitic composition. Most basalticandesite lavas at Azufre and Planchon are related by a plagioclase-poor,anhydrous mineral fractionating assemblage. High-alumina basaltis produced from a tholeiitic parent by an 4–8 kbar fractionatingassemblage. During this moderatepressure crystallization, themagmas also incorporated a crustal component with high La/Yband high abundances of Rb, Cs and Th. Based on the chemicalcharacteristics of the added component and the inferred depthof crystallization, the crustal source may have been garnetgranulite derived from solidified arc magmas in the lower tomiddle continental crust. At Planchon, the role of crustal assimilationhas increased with decreasing eruption age probably becausecrustal temperatures have increased during continued volcanism.Azufre dacite lavas formed at low pressures by fractionationof a plagioclase-rich assemblage. These dacite lavas containan upper-crustal component, probably derived in part from limestone,with high values of ⁸⁷Sr/⁸⁶Sr and ¹⁸O/¹⁶O. Thus two depths (upperand lower crust) of crystallization and associated crustal assimilationare evident in Planchon–Azufre lavas. Peteroa, the focusof recent volcanism, consists of calc-alkaline andesite anddacite eruptive products whose textures and compositions indicatean important role for magma mixing. Therefore, the volcanismevolved from a tholeiitic system of basalt and subordinate dacite(Planchon–Azufre) to a calc-alkaline system with abundantmixed lavas of intermediate composition (Peteroa). In additionto crustal thickness, two important parameters which controlledthe diversity of lava composition in this complex are magmasupply rate from the mantle and crustal temperature. Both parametersvaried with time, and they must be considered in broader interpretationsof along-strike geochemical trends. KEY WORDS: arc magmas; Andes; Peteroa; Planchan; geochemistry ^*Corresponding author. Present address: ENTRIX, Inc., 4II North Central Avenue, Glendale, CA 91203, USA     

Cenozoic alkali basaltic magmas of western Germany and their products of differentiation

Analytical data on major elements and 31 trace elements in olivine nephelinites, nepheline basanites, basanitic alkali olivine basalts and their differentiates (tephrites, hawaiites, mugearites, benmoreites, latites, phonolites and trachytes) from Hegau, Kaiserstuhl, Rhön, Hessian Depression, Vogelsberg, Westerwald, Siebengebirge, E Eifel and Hocheifel are evaluated. They were based on 400 samples with new or unpublished data on about one third of the rocks. The Sr–Nd isotopic compositions for 78 rocks are included. The alkali basaltic volcanism is caused by adiabatic decompression of asthenospheric mantle updomed to a minimum depth of 50 km in connection with the Alpine continent collision. The chemical compositions of the primary basaltic melts from the different areas are similar containing about one hundred-fold enrichment of highly incompatible elements relative to the primitive mantle from partial melting of depleted and secondarily enriched peridotite. The elements Cs, K, Pb and Ti are specifically depleted in the basalts partly because of phlogopite being residual at partial melting. The Tertiary alkali basalts range in Nd-isotopic composition from 0.51288 to 0.51273 and in Sr-isotopic ratios from 0.7032 to 0.7042. These ranges indicate mixtures of HIMU, depleted and enriched mantle components in the metasomatically altered peridotite source which resembles that of certain ocean islands. The Nd-Sr-isotopic compositions of the Quaternary E Eifel are close to bulk Earth ratios. East and W Eifel plots differ distinctly from the Tertiary Hocheifel which is geographically intermediate. This isotopic difference, beside specific K/Na ratios, is probably caused by separate metasomatic pulses that immediately preceded the respective periods of volcanism. The metasomatically altered mantle had partly primitive mantle signatures (Nb/Ta, Zr/Sm and Th/U ratios) and partly ocean island (or MORB) source properties (Rb/Cs). A MORB source can be excluded because of the low K/Rb and high Th/U ratios. A correlation of D with ⁸⁷Sr/⁸⁶Sr in amphibole and phlogopite and a slightly larger ¹⁸O than in MORB is conformable with a seawater and crustal impact on the source of alkali basalts. Slightly higher than average water concentrations in the source of certain primary basaltic melts (indicated by amphibole phenocrysts in their basalts) are required for differentiation of these basalts in magma chambers of the upper crust. Model calculations are presented to explain compositions of differentiates which range from about 60% to about 20% residual melt. The latter are represented by phonolites and trachytes. The Nd- and Sr-isotopic signatures of the majority of differentiates indicate contamination by a granitic partial melt from the wall rocks of magma chambers. Olivine nephelinite magma was the common source of contaminated differentiates.     

The Role of Lithospheric Mantle Heterogeneity in the Generation of Plio-Pleistocene Alkali Basaltic Suites from NW Harrat Ash Shaam (Israel)

Plio-Pleistocene volcanism in the Golan and Galilee (northeasternIsrael) shows systematic variability with time and location:alkali basalts were erupted in the south during the Early Pliocene,whereas enriched basanitic lavas erupted in the north duringthe Late Pliocene (Galilee) and Pleistocene (Golan). The basaltsshow positive correlations in plots of ratios of highly to moderatelyincompatible elements versus the concentration of the highlyincompatible element (e.g. Nb/Zr vs Nb, La/Sm vs La) and indiagrams of REE/HFSE (rare earth elements/high field strengthelements) vs REE concentration (e.g. La/Nb vs La). Some of thesecorrelations are not linear but upward convex. ⁸⁷Sr/⁸⁶Sr ratiosvary between 0·7031 and 0·7034 and correlate negativelywith incompatible element concentrations and positively withRb/Sr ratios. We interpret these observations as an indicationthat the main control on magma composition is binary mixingof melts derived from two end-member mantle source components.Based on the high Sr/Ba ratios and negative Rb anomalies inprimitive mantle normalized trace element diagrams and the moderateslopes of MREE–HREE (middle REE–heavy REE) in chondrite-normalizeddiagrams, we suggest that the source for the alkali basalticend-member was a garnet-bearing amphibole peridotite that hadexperienced partial dehydration. The very high incompatibleelement concentrations, low K content, very low Rb contentsand steep MREE–HREE patterns in the basanites are attributedto derivation from amphibole- and garnet-bearing pyroxeniteveins. It is suggested that the veins were produced via partialmelting of amphibole peridotites, followed by complete solidificationand dehydration that effectively removed Rb and K. The requirementfor the presence of amphibole limits both sources to lithosphericdepths. The spatial geochemical variability of the basalts indicatesthat the lithosphere beneath the region is heterogeneous, composedof vein-rich and vein-poor domains. The relatively uniform ¹⁴³Nd/¹⁴⁴Nd(Nd = 4·0–5·2) suggests that the two mantlesources were formed by dehydration and partial melting of anoriginally isotopically uniform reservoir, probably as a resultof a Paleozoic thermal event. KEY WORDS: basanites; lithospheric heterogeneity; magma mixing; amphibole peridotite; pyroxenites     

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     

Strontium isotope studies on young volcanic rocks from Germany and Italy

⁸⁷Sr/⁸⁶Sr ratios of Tertiary tholeiitic, basalts alkali olivine basalts and olivine nephelinites from Lower Saxony and Hessia and Quaternary leucite-nepheline tephrites from the Laacher See area are similar to those obtained from Hawaii and range from 0.7031 to 0.7054. Three trachytes and one phonolite from the Westerwald and one phonolite from the Laacher See area have higher values (0.7063 to 0.7093). Three Vesuvian lavas, three Somma lavas and two trachytes of the Phlegraic Fields show substantially higher ratios than the comparable basaltic rocks from N.W. Germany (0.7071 to 0.7102). Three peridotite nodules vary between 0.7048 and 0.7081. Three limestone composites of Paleozoic and Mesozoic age show values between 0.7129 and 0.7174.The ⁸⁷Sr/⁸⁶Sr ratios of the trachytes and phonolites from the Westerwald and Laacher See area are probably influenced by crustal material. Assimilation processes of limestones producing the olivine-nephelinites from N.W. Germany seem to be unlikely. A discussion of the origin of the Sr ratios in Vesuvian rocks and of mantle homogeneity is included.     

Tertiary basalts and peridotite xenoliths from the Hessian Depression (NW Germany), reflecting mantle compositions low in radiogenic Nd and Sr

A total of 17 alkali basalts (alkali olivine basalt, limburgite, olivine nephelinite) and quartz tholeiites, and of 10 peridotite xenoliths (or their clinopyroxenes) were analyzed for Nd and Sr isotopes. ¹⁴³Nd/¹⁴⁴Nd ratios and ⁸⁷Sr/⁸⁶Sr ratios of all basalts and of the majority of ultramafic xenoliths plot below the mantle array with a large variation in Nd isotopes and a smaller variation in Sr isotopes. The tholeiites were less radiogenic in Nd than the alkali basalts. Volcanics from the Eifel and Massif Central regions contain Nd and Sr, which is more radiogenic than that of the basalts from the Hessian Depression. Nd and Sr isotopic compositions of all rocks from the latter area, with the exception of one tholeiite and one peridotite plot in the same field of isotope ratios as the Ronda ultramafic tectonite (SW Spain), which ranges in composition from garnet to plagioclase peridotite. The alkali basaltic rocks are products of smaller degrees of partial melting of depleted peridotite, which has undergone a larger metasomatic alteration compared with the source rock of tholeiitic magmas. For the peridotite xenoliths such metasomatic alteration is indicated by the correlation of their K contents and isotopic compositions. We assume that the upper mantle locally can acquire isotopic signatures low in radiogenic Nd and Sr from the introduction of delaminated crust. Such granulites low in radiogenic Nd and Sr are products of early REE fractionation and granite (Rb) separation.     

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     

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     

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     

The Petrogenesis of Pliocene Alkaline Volcanic Rocks from the Pannonian Basin, Eastern Central Europe

Late Tertiary post-orogenic alkaline basalts erupted in theextensional Pannonian Basin following Eocene-Miocene subductionand its related calc-alkaline volcanism. The alkaline volcaniccentres, dated between 11•7 and 1•4 Ma, are concentratedin several regions of the Pannonian Basin. Some are near thewestern (Graz Basin, Burgenland), northern (Ngrd), and eastern(Transylvania) margins of the basin, but the majority are concentratednear the Central Range (Balaton area and Little Hungarian Plain).Fresh samples from 31 volcanic centres of the extension-relatedlavas range from slightly hy-normative transitional basaltsthrough alkali basalts and basanites to olivine nephelinites.No highly evolved compositions have been encountered. The presenceof peridotite xenoliths, mantle xenocrysts, and high-pressuremegacrysts, even in the slightly more evolved rocks, indicatesthat differentiation took place within the upper mantle. Rare earth elements (REE) and ⁸⁷Sr/⁸⁶Sr, ¹⁴³Nd/¹⁴⁴Nd, ¹⁸O, D,and Pb isotopic ratios have been determined on a subset of samples,and also on clinopyroxene and amphibole megacrysts. Sr and Ndisotope ratios span the range of Neogene alkali basalts fromwestern and central Europe, and suggest that the magmas of thePannonian Basin were dominantly derived from asthenosphericpartial melting, but Pb isotopes indicate that in most casesthey were modified by melt components from the enriched lithosphericmantle through which they have ascended. ¹⁸O values indicatethat the magmas have not been significantly contaminated withcrustal material during ascent, and isotopic and trace-elementratios therefore reflect mantle source characteristics. Incompatible-elementpatterns show that the basic lavas erupted in the Balaton areaand Little Hungarian Plain are relatively homogeneous and areenriched in K, Rb, Ba, Sr, and Pb with respect to average oceanisland basalt, and resemble alkali basalts of Gough Island.In addition, ²⁰⁷Pb/²⁰⁴Pb is enriched relative to ^2O6Pb/²⁰⁴Pb.In these respects, the lavas of the Balaton area and the LittleHungarian Plain differ from those of other regions of Neogenealkaline magmatism of Europe. This may be due to the introductionof marine sediments into the mantle during the earlier periodof subduction and metasomatism of the lithosphere by slab-derivedfluids rich in K, Rb, Ba, Pb, and Sr. Lavas erupted in the peripheralareas have incompatible-element patterns and isotopic characteristicsdifferent from those of the central areas of the basin, andmore closely resemble Neogene alkaline lavas from areas of westernEurope where recent subduction has not occurred.     

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     

Petrogenesis of Basanitic to Tholeiitic Volcanic Rocks from the Miocene Vogelsberg, Central Germany

The Miocene Vogelsberg volcano in Central Germany produced maficmagmas ranging in composition from basanite to quartz tholeiiteand limited amounts of evolved magmas. Trace element and Nd,Sr and Pb isotopic compositions reveal the presence of threedistinct mantle sources: (1) a trace element enriched, asthenosphericplume-type source, similar to the European Asthenospheric Reservoircomposition inferred for many other Tertiary volcanic provincesin Central Europe; (2) a depleted mantle source, located inthe lithospheric mantle or uppermost asthenosphere; (3) a veinedlithospheric mantle source. The oldest basanites of the Vogelsbergvolcano have distinctly higher Ti, Al, Sc and V contents thanyounger basanites. These high-Ti basanites may have been producedby partial melting of a veined lithospheric mantle source, formedduring the earliest stages of uplift of the Rhenish Shield,     

The Cameroon Volcanic Line Revisited: Petrogenesis of Continental Basaltic Magmas from Lithospheric and Asthenospheric Mantle Sources

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

Contemporaneous Convergent Margin and Intraplate Magmatism, North Island, New Zealand

A convergent margin magma series with characteristic low Nband Ta abundances and enrichments in alkalis and alkaline earthsis intercalated with typical intraplate alkalic basalts in aback-arc setting, 200–250 km above the Wadati-Benioffzone on the North Island, New Zealand. These two contrastingmagma types, together with late-stage K-rich maflc lavas, wereerupted over a short time period (1{dot}60–2{dot}74 Ma)and constitute the Alexandra Volcanics. Field relationshipsindicate that these diverse magma types were contemporaneous,and thus their mantle source regions coexisted, in a singletectonic environment. The convergent margin magma series forms a linear chain of stratovolcanoesaligned at right angles to the present subduction zone. Closed-systempolybaric fractional crystallization models can explain theevolution from ankaramites to transitional olivine basalts toolivine tholeiites to high-Al basalts to medium- and high-Kandesites. The most primitive lavas have geochemical (high LIL/LREEand LIL/HFS element ratios) and Sr, Nd, and Pb isotopic compositionstypical of convergent margin magmas. Calculated source compositionssuggest that three components are involved: a MORB component,a component derived from subducted oceanic crust, and a contributionfrom subducted sediments. The alkalic basalts occur as dispersed monogenetic volcanoesand are intercalated with the larger convergent margin stratovolcanocs.These basalts are enriched in LILE, LREE, Nb, and Ta, and havelow Ba/Nb and Ba/La ratios, all of which are characteristicof ocean island (intraplate) basalts (OIBs). Their relativelyhigh _Nd (+5{dot}5 and low ⁸⁷Sr/⁸⁶Sr(0{dot}703l–0{dot}7036)are also typical of OIBs. These alkalic magmas were derivedfrom the underlying continental lithospheric mantle that hasbeen enriched by upward-migrating silica-undersaturated melts,probably including volatiles, from the low- velocity zone. Asubducted slab component is not required to account for theirincompatible element enriched character. The K-rich mafic lavas, basanites, and absarokites are volumetricallyminor and cap the largest of the stratovolcanoes, Pirongia.The basanites have geochemical and isotopic compositions whichsuggest they are mixtures of multiple source components, includingthe alkalic and convergent margin region.     

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     

Rapid Temporal Changes in Ocean Island Basalt Composition: Evidence from an 800 m Deep Drill Hole in Eiao Shield (Marquesas)

The Dominique drill hole has penetrated the volcanic shieldof Eiao island (Marquesas) down to a depth of 800 m below thesurface and 691•5 m below sea-level with a percentage ofrecovery close to 100%. All the lavas encountered were emplacedunder subaerial conditions. From the bottom to the top are distinguished:quartz and olivine tholeiites (800–686 m), hawaiites,mugearites and trachyte (686–415 m), picritic basalts,olivine tholeiites and alkali basalts (415–0 m). The coredvolcanic pile was emplaced between 5•560•07 Ma and5•220•06 Ma. Important chemical changes occurred during this rather shorttime span (0•34 0•13 Ma). In particular, the lowerbasalts differ from the upper ones in their lower concentrationsof incompatible trace elements and their Sr, Nd and Pb isotopicsignature being closer to the HIMU end-member, whereas the upperbasalts are EM II enriched. The chemical differences betweenthe two basalt groups are consistent with a time-related decreasein the degree of partial melting of isotopically heterogeneoussources. It seems unlikely that these isotopic differences reflectchanges in plume dynamics occurring in such a short time span,and we tentatively suggest that they result from a decreasingdegree of partial melting of a heterogeneous EM II–HIMUmantle plume. Some of the intermediate magmas (the uppermost hawaiites andmugearites) are likely to be derived from parent magmas similarto the associated upper basalts through simple fractionationprocesses. Hawaiites, mugearites and a trachyte from the middlepart of the volcanic sequence have Sr–Nd isotopic signaturessimilar to those of the lower basalts but they differ from themin their lower ²⁰⁶Pb/²⁰⁴Pb ratios, resulting in an increasedDMM signature. Some of the hawaiites-mugearites also displayspecific enrichments in P₂O₅, Sr and REE which are unlikelyto result from simple fractionation processes. The isotopicand incompatible element compositions of the intermediate rocksare consistent with the assimilation of MORB-derived wall rocksduring fractional crystallization. The likely contaminant correspondsto Pacific oceanic crust, locally containing apatite-rich veinsand hydrothermal sulphides. We conclude that a possible explanationfor the DMM signature in ocean island basalts is a chemicalcontribution from the underlying oceanic crust and that studiesof intermediate rocks may be important to document the originof the isotopic features of plume-derived magmas. KEY WORDS: alkali basalt; assimilation; mantle heterogeneity; Marquesas; tholeiile ^*Corresponding author     

Geochemistry, Petrogenesis and Geodynamic Relationships of Miocene Calc-alkaline Volcanic Rocks in the Western Carpathian Arc, Eastern Central Europe

We report major and trace element abundances and Sr, Nd andPb isotopic data for Miocene (16·5–11 Ma) calc-alkalinevolcanic rocks from the western segment of the Carpathian arc.This volcanic suite consists mostly of andesites and dacites;basalts and basaltic andesites as well as rhyolites are rareand occur only at a late stage. Amphibole fractionation bothat high and low pressure played a significant role in magmaticdifferentiation, accompanied by high-pressure garnet fractionationduring the early stages. Sr–Nd–Pb isotopic dataindicate a major role for crustal materials in the petrogenesisof the magmas. The parental mafic magmas could have been generatedfrom an enriched mid-ocean ridge basalt (E-MORB)-type mantlesource, previously metasomatized by fluids derived from subductedsediment. Initially, the mafic magmas ponded beneath the thickcontinental crust and initiated melting in the lower crust.Mixing of mafic magmas with silicic melts from metasedimentarylower crust resulted in relatively Al-rich hybrid dacitic magmas,from which almandine could crystallize at high pressure. Theamount of crustal involvement in the petrogenesis of the magmasdecreased with time as the continental crust thinned. A strikingchange of mantle source occurred at about 13 Ma. The basalticmagmas generated during the later stages of the calc-alkalinemagmatism were derived from a more enriched mantle source, akinto FOZO. An upwelling mantle plume is unlikely to be presentin this area; therefore this mantle component probably residesin the heterogeneous upper mantle. Following the calc-alkalinemagmatism, alkaline mafic magmas erupted that were also generatedfrom an enriched asthenospheric source. We propose that bothtypes of magmatism were related in some way to lithosphericextension of the Pannonian Basin and that subduction playedonly an indirect role in generation of the calc-alkaline magmatism.The calc-alkaline magmas were formed during the peak phase ofextension by melting of metasomatized, enriched lithosphericmantle and were contaminated by various crustal materials, whereasthe alkaline mafic magmas were generated during the post-extensionalstage by low-degree melting of the shallow asthenosphere. Thewestern Carpathian volcanic areas provide an example of long-lastingmagmatism in which magma compositions changed continuously inresponse to changing geodynamic setting. KEY WORDS: Carpathian–Pannonian region; calc-alkaline magmatism; Sr, Nd and Pb isotopes; subduction; lithospheric extension