A 5 million year record of compositional variations in mantle sources to magmatism on Santiago, southern Cape Verde archipelago

High-precision Pb isotope data and Sr–Nd–Hf isotope data are presented together with major and trace element data for samples spanning the 4.6 Ma history of volcanism at Santiago, in the southern Cape Verde islands. Pb isotope data confirm the positive Δ8/4 signature of the southern islands indicating that the north–south compositional heterogeneity in the Cape Verde archipelago has persisted for at least 4.6 Ma. The Santiago volcanics show distinct compositional differences between the old, intermediate and young volcanics, and suggest greater involvement of an enriched mantle (EM1)-like source over time. Isotopic variations in the Santiago volcanics indicate convergence towards a homogeneous EM1-like end-member and distinct temporal variations in the FOZO-like end-member. Santiago and Santo Antão (a northern island, Holm et al. 2006), show a simultaneous decrease in ²⁰⁸Pb/²⁰⁴Pb of the high ²⁰⁶Pb/²⁰⁴Pb FOZO-like source with time. Such systematic archipelago-wide variations in the FOZO-like component suggest that this component is more likely to be present as a coherent package of recycled ocean crust rather than as multiple small heterogeneities dispersed in the upwelling mantle. The temporal variations in ²⁰⁸Pb/²⁰⁴Pb reflect minor lateral variations in Th/U of this recycled ocean crust package entering the melting zone beneath the islands. The location of the EM1-like component is more equivocal. A shallow lithospheric location is possible, but this would require a coincidence between spatial compositional variations in the lithosphere (EM1 is spatially restricted to the southern islands) and flow lines in the upwelling mantle revealed by seismic anisotropy. Therefore, we favour a deeper asthenospheric mantle source for the EM1-like source.     

Origin of submarine volcanism at the eastern margin of the central atlantic: Investigation of the alkaline volcanic rocks of the carter seamount (Grimaldi Seamounts)

This paper addresses the composition, geochemistry, isotopic characteristics, and age of rocks from the Carter Seamount of the Grimaldi seamount group at the eastern margin of the Central Atlantic. The age of the seamount was estimated as 57–58 Ma. Together with other seamounts of the Grimaldi system and the Nadir Seamount, it forms a “hot line” related to the Guinea Fracture Zone, which was formed during the late Paleocene pulse of volcanism. The Carter Seamount is made up of olivine melilitites, ankaramites, and analcime-bearing nepheline tephrites, which are differentiated products of the fractional crystallization of melts similar to an alkaline ultramafic magma. The volcanics contain xenoliths entrained by melt at different depths from the mantle, layer 3 of the oceanic crust, which was formed at 113–115 Ma, and earlier magma chambers. The rocks were altered by low-temperature hydrothermal solutions. The parental melts of the volcanics of the Carter Seamount were derived at very low degrees of mantle melting in the stability field of garnet lherzolite at depths of no less than 105 km. Anomalously high Th, Nb, Ta, and La contents in the volcanics indicate that a metasomatized mantle reservoir contributed to the formation of their primary melts. The Sr, Pb, and Nd isotopic systematics of the rocks show that the composition of the mantle source lies on the mixing line between two mantle components. One of them is a mixture of prevailing HIMU and the depleted mantle, and the other is an enriched EM2-type mantle reservoir. These data suggest that the formation of the Carter Seamount volcanics was caused by extension-related decompression melting in the Guinea Fracture Zone of either (1) hot mantle plume material (HIMU component) affected by carbonate metasomatism or (2) carbonated basic enclaves (eclogites) ubiquitous in the asthenosphere, whose isotopic characteristics corresponded to the HIMU and EM2 components. In the former case, it is assumed that the melt assimilated during ascent the material of the metasomatized subcontinental mantle (EM2 component), which was incorporated into the oceanic lithospheric mantle during rifting and the breakup of Pangea.     

Pb-Sr-He isotope and trace element geochemistry of the Cape Verde Archipelago

New lead, strontium and helium isotopic data, together with trace element concentrations, have been determined for basalts from the Cape Verde archipelago (Central Atlantic). Isotopic and chemical variations are observed at the scale of the archipelago and lead to the definition of two distinct groupings, in keeping with earlier studies. The Northern Islands (Santo Antão, São Vicente, São Nicolau and Sal) present Pb isotopic compositions below the Northern Hemisphere Reference Line (NHRL) (cf. Hart, 1984), unradiogenic Sr and relatively primitive ⁴He/³He ratios. In contrast, the Southern Islands (Fogo and Santiago) display Pb isotopes above the NHRL, moderately radiogenic Sr and MORB-like helium signatures. We propose that the dichotomy between the Northern and Southern Islands results from the presence of three isotopically distinct components in the source of the Cape Verde basalts: (1) recycled ∼1.6-Ga oceanic crust (high ²⁰⁶Pb/²⁰⁴Pb, low ⁸⁷Sr/⁸⁶Sr and high ⁴He/³He); (2) lower mantle material (high ³He); and (3) subcontinental lithosphere (low ²⁰⁶Pb/²⁰⁴Pb, high ⁸⁷Sr/⁸⁶Sr and moderately radiogenic ⁴He/³He ratios). The signature of the Northern Islands reflects mixing between recycled oceanic crust and lower mantle, to which small proportions of entrained depleted material from the local upper mantle are added. Basalts from the Southern Islands, however, require the addition of an enriched component thought to be subcontinental lithospheric material instead of depleted mantle. The subcontinental lithosphere may stem from delamination and subsequent incorporation into the Cape Verde plume, or may be remnant from delamination just before the opening of the Central Atlantic. Basalts from São Nicolau reflect the interaction with an additional component, which is identified as oceanic crustal material.     

Magma storage and ascent during the 1995 eruption of Fogo,Cape Verde Archipelago

The 1995 eruption of Fogo (Cape Verde Islands) differed from previous eruptions by the occurrence of evolved lavas, the SW-orientation of vents, and pre-eruptive seismicity between Fogo and the adjacent (~20 km) island of Brava. We have conducted a thermobarometric and chemical study of this eruption in order to reconstruct its magma plumbing system and to test for possible connections to Brava. The bimodal eruption produced basanites (5.2–6.7 wt% MgO) and phonotephrites (2.4–2.8 wt% MgO) that are related by fractional crystallization. Clinopyroxene-melt-barometry of phenocrysts yields pressure ranges of 460–680 MPa for the basanites and 460–520 MPa for the phonotephrites. Microthermometry of CO₂-dominated fluid inclusions in olivine and clinopyroxene phenocrysts yields systematically lower pressure ranges of 200–310 MPa for basanites and 270–470 MPa for phonotephrites. The combined data indicate pre-eruptive storage of the 1995 magmas within the lithospheric mantle between 16 and 24 km depth. During eruption, the ascending magmas stalled temporarily at 8–11 km depth, within the lower crust, before they ascended to the surface in a few hours as indicated by zonations of olivine phenocrysts. Our data provide no evidence for magma storage at shallow levels (<200 MPa) or lateral magma movements beneath the Fogo-Brava platform. Sr–Nd–Pb isotope ratios of samples from Brava differ significantly from those of the 1995 and older Fogo lavas, which rules out contamination of the 1995 magmas by Brava material and indicates different mantle sources and magma plumbing systems for both islands.     

Geochemical constraints on depth of origin of oceanic carbonatites: The Cape Verde case

We present new Sr-Nd isotope compositions together with major- and trace element concentrations measured for whole rocks and mineral separate phases (apatite, biotite and calcite) from fifteen Cape Verde oceanic carbonatites (Atlantic Ocean). Trace element patterns of calcio- and magnesio-carbonatites present a strong depletion in K, Hf, Zr and Ti and an overall enrichment in Sr and REE relative to Cape Verde basalts, arguing for distinct source components between carbonatites and basalts. Sr and Nd isotopic ratios show small, but significant variations defining a binary mixing between a depleted end-member with unradiogenic Sr and radiogenic Nd values and a ‘‘enriched’’ end-member compatible with old marine carbonates. We interpret the depleted end-member as the Cape Verde oceanic lithosphere by comparison with previous studies on Cape Verde basalts. We thus propose that oceanic carbonatites are resulting from the interaction of a deep rooted mantle plume carrying a lower ⁴He/³He signature from the lower mantle and a carbonated metasomatized lithosphere, which by low degree melting produced carbonatite magmas. Sr-Nd compositions and trace element patterns of carbonatites argue in favor of a metasomatic agent originating from partial melting of recycled, carbonated oceanic crust. We have successfully reproduced the main geochemical features of this model using a Monte-Carlo-type simulation.     

Geochemistry of oceanic carbonatites compared with continental carbonatites: mantle recycling of oceanic crustal carbonate

Major and trace element and Sr-Nd-Pb-O-C isotopic compositions are presented for carbonatites from the Cape Verde (Brava, Fogo, Sáo Tiago, Maio and Sáo Vicente) and Canary (Fuerteventura) Islands. Carbonatites show pronounced enrichment in Ba, Th, REE, Sr and Pb in comparison to most silicate volcanic rocks and relative depletion in Ti, Zr, Hf, K and Rb. Calcio (calcitic)-carbonatites have primary (mantle-like) stable isotopic compositions and radiogenic isotopic compositions similar to HIMU-type ocean island basalts. Cape Verde carbonatites, however, have more radiogenic Pb isotope ratios (e.g. ²⁰⁶Pb/²⁰⁴Pb=19.3-20.4) than reported for silicate volcanic rocks from these islands (18.7-19.9; Gerlach et al. 1988; Kokfelt 1998). We interpret calcio-carbonatites to be derived from the melting of recycled carbonated oceanic crust (eclogite) with a recycling age of ~1.6 Ga. Because of the degree of recrystallization, replacement of calcite by secondary dolomite and elevated ‘¹³C and ‘¹⁸O, the major and trace element compositions of the magnesio (dolomitic)-carbonatites are likely to reflect secondary processes. Compared with Cape Verde calcio-carbonatites, the less radiogenic Nd and Pb isotopic ratios and the negative Ɨ/4 of the magnesio-carbonatites (also observed in silicate volcanic rocks from the Canary and Cape Verde Islands) cannot be explained through secondary processes or through the assimilation of Cape Verde crust. These isotopic characteristics require the involvement of a mantle component that has thus far only been found in the Smoky Butte lamproites from Montana, which are believed to be derived from subcontinental lithospheric sources. Continental carbonatites show much greater variation in radiogenic isotopic composition than oceanic carbonatites, requiring a HIMU-like component similar to that observed in the oceanic carbonatites and enriched components. We interpret the enriched components to be Phanerozoic through Proterozoic marine carbonate (e.g. limestone) recycled through shallow, subcontinental-lithospheric-mantle and deep, lower-mantle sources.     

Nd,Pb, and Sr isotope composition of Late Mesozoic to Quaternary intra-plate magmatism in NE-Africa (Sudan,Egypt): high-μ signatures from the mantle lithosphere

The isotopic composition of mafic small-volume intra-plate magmatism constrains the compositions of the sub-continental mantle sources. The Nd, Pb, and Sr isotope signatures of widespread late Mesozoic to Quaternary intra-plate magmatism in NE Africa (Sudan, South Egypt) are surprisingly uniform and indicate the presence of a high-μ (μ = ²³⁸U/²⁰⁴Pb) source in the mantle. The rocks are characterized by small ranges in the initial isotopic composition of Nd, Pb, and Sr and most samples fall within ε Nd ca. 3–6, ²⁰⁶Pb/²⁰⁴Pb ca. 19.5–20.5, ²⁰⁷Pb/²⁰⁴Pb ca. 15.63–15.73, ²⁰⁸Pb/²⁰⁴Pb ca. 39–40 and ⁸⁷Sr/⁸⁶Sr ca. 0.7028–0.7034. We interpret this reservoir as lithospheric mantle that formed beneath the Pan-African orogens and magmatic arcs from asthenospheric mantle, which was enriched in trace elements (U, Th, and light REE). Combining our new data set with published data of intra-plate magmatic rocks from the Arabian plate indicates two compositionally different domains of lithospheric mantle in NE-Africa–Arabia. The two domains are spatially related to the subdivision of the Pan-African orogen into a western section dominated by reworked cratonic basement (NE-Africa; high-μ lithospheric mantle) and an eastern section dominated by juvenile Pan-African basement (easternmost NE-Africa and Arabia; moderate μ lithospheric mantle). The compositions of the Pan-African lithospheric mantle and the MORB-type mantle of the Red Sea and Gulf of Aden spreading centers could explain the Nd–Pb-Sr isotopic compositions of the most pristine Afar flood basalts in Yemen and Ethiopia by mixtures of the isotopic composition of regional lithospheric and asthenospheric sources. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Geochemical Stratigraphy of Submarine Lavas (3-5 Ma) from the Flamengos Valley, Santiago, Southern Cape Verde Islands

New high-precision Pb–Sr–Nd isotope, major and traceelement and mineral chemistry data are presented for the submarinestage of ocean island volcanism on Santiago, one of the southernislands of the Cape Verde archipelago. Pillow basalts and hyaloclastitesin the Flamengos Valley are divided into three petrographicand compositional groups; the Flamengos Formation lavas (4·6Ma) dominate the sequence, with the younger Low Si and Coastalgroups (2·8 Ma) found near the shoreline. Olivine andclinopyroxene compositions and isotopic data for minerals andtheir host melts indicate disequilibrium between some crystalsand the melt. Intra-sample disequilibrium suggests homogenisationof liquids but eruption before complete equilibration betweencrystals and melt preserves the heterogeneity. Pressures ofcrystallization for clinopyroxene (0·4–1·1GPa) indicate stalling and crystallization of the magmas overa range of depths in the lithosphere. Major element compositionsindicate melting of a carbonated eclogite source. Sr–Nd–Pbisotope data suggest the involvement of FOZO-like and EM1-likecomponents in the mantle source, which are simultaneously availableat all depths in the melting column. The Flamengos Valley lavasdisplay large compositional variations, often between stratigraphicallyadjacent flows; these frequent abrupt changes of magma compositionsuggest stalling and crystallization of discrete magma batcheson transport through the lithosphere. KEY WORDS: Cape Verde; crystal–melt disequilibrium; submarine volcanism; source heterogeneity; Pb–Sr–Nd isotopes     

Petrogenesis of the Neogene volcanic units in the NE–SW-trending basins in western Anatolia,Turkey

The western Anatolian volcanic province formed during Eocene to Recent times is one of the major volcanic belts in the Aegean–western Anatolian region. We present new chemical (whole-rock major and trace elements, and Sr, Nd, Pb and O isotopes) and new Ar/Ar age data from the Miocene volcanic rocks in the NE–SW-trending Neogene basins that formed on the northern part of the Menderes Massif during its exhumation as a core complex. The early-middle Miocene volcanic rocks are classified as high-K calc-alkaline (HKVR), shoshonitic (SHVR) and ultrapotassic (UKVR), with the Late Miocene basalts being transitional between the early-middle Miocene volcanics and the Na-alkaline Quaternary Kula volcanics (QKV). The early-middle Miocene volcanic rocks are strongly enriched in large ion lithophile elements (LILE), have high ⁸⁷Sr/⁸⁶Sr_(i) (0.70631–0.71001), low ¹⁴³Nd/¹⁴⁴Nd_(i) (0.512145–0.512488) and high Pb isotope ratios (²⁰⁶Pb/²⁰⁴Pb = 18.838–19.148; ²⁰⁷Pb/²⁰⁴Pb = 15.672–15.725; ²⁰⁸Pb/²⁰⁴Pb = 38.904–39.172). The high field strength element (HFSE) ratios of the most primitive early-middle Miocene volcanic rocks indicate that they were derived from a mantle source with a primitive mantle (PM)-like composition. The HFSE ratios of the late Miocene basalts and QKV, on the other hand, indicate an OIB-like mantle origin—a hypothesis that is supported by their trace element patterns and isotopic compositions. The HFSE ratios of the early-middle Miocene volcanic rocks also indicate that their mantle source was distinct from those of the Eocene volcanic rocks located further north, and of the other volcanic provinces in the region. The mantle source of the SHVR and UKVR was influenced by (1) trace element and isotopic enrichment by subduction-related metasomatic events and (2) trace element enrichment by “multi-stage melting and melt percolation” processes in the lithospheric mantle. The contemporaneous SHVR and UKVR show little effect of upper crustal contamination. Trace element ratios of the HKVR indicate that they were derived mainly from lower continental crustal melts which then mixed with mantle-derived lavas (~20–40%). The HKVR then underwent differentiation from andesites to rhyolites via nearly pure fractional crystallization processes in the upper crust, such that have undergone a two-stage petrogenetic evolution.     

Geochemistry of Lavas from the Emperor Seamounts, and the Geochemical Evolution of Hawaiian Magmatism from 85 to 42 Ma

The Hawaiian–Emperor Seamount Chain (ESC), in the northernPacific Ocean, was produced during the passage of the PacificPlate over the Hawaiian hotspot. Major and trace element concentrationsand Sr–Nd–Pb isotopic compositions of shield andpost-shield lavas from nine of the Emperor Seamounts providea 43 Myr record of the chemistry of the oldest preserved Hawaiianmagmatism during the Late Mesozoic and Early Cenozoic (from85 to 42 Ma). These data demonstrate that there were large variationsin the composition of Hawaiian magmatism over this period. Tholeiiticbasalts from Meiji Seamount (85 Ma), at the northernmost endof the ESC, have low concentrations of incompatible trace elements,and unradiogenic Sr isotopic compositions, compared with youngerlavas from the volcanoes of the Hawaiian Chain (<43 Ma).Lavas from Detroit Seamount (81 Ma) have highly depleted incompatibletrace element and Sr–Nd isotopic compositions, which aresimilar to those of Pacific mid-ocean ridge basalts. Lavas fromthe younger Emperor Seamounts (62–42 Ma) have trace elementcompositions similar to those of lavas from the Hawaiian Islands,but initial ⁸⁷Sr/⁸⁶Sr ratios extend to lower values. From 81to 42 Ma there was a systematic increase in ⁸⁷Sr/⁸⁶Sr of boththoleiitic and alkalic lavas. The age of the oceanic lithosphereat the time of seamount formation decreases northwards alongthe Emperor Seamount Chain, and the oldest Emperor Seamountswere built upon young, thin lithosphere close to a former spreadingcentre. However, the inferred distance of the Hawaiian plumefrom a former spreading centre, and the isotopic compositionsof the oldest Emperor lavas appear to rule out plume–ridgeinteraction as an explanation for their depleted compositions.We suggest that the observed temporal chemical and isotopicvariations may instead be due to variations in the degree ofmelting of a heterogeneous mantle, resulting from differencesin the thickness of the oceanic lithosphere upon which the EmperorSeamounts were constructed. During the Cretaceous, when theHawaiian plume was situated beneath young, thin lithosphere,the degree of melting within the plume was greater, and incompatibletrace element depleted, refractory mantle components contributedmore to melting. KEY WORDS: Emperor Seamounts; Hawaiian plume; lava geochemistry; lithosphere thickness; mantle heterogeneity     

U–Pb zircon dating, geochemical and Sr–Nd–Hf isotopic compositions of Early Indosinian intrusive rocks in West Qinling, central China: petrogenesis and tectonic implications

The Qinling–Dabie–Sulu orogenic belt is the junction between the North and South China blocks, which resulted from the final amalgamation of China continents during the Indosinian. Indosinian granitoids are widespread in the Qinling orogen, and their geneses can thus constrain the evolution of China continent. We carried out a combined U–Pb zircon dating and geochemical study for the Shuangpengxi granodiorite pluton and the Xiekeng diorite–granodiorite pluton in the middle part of the West Qinling orogen. U–Pb zircon dating shows that the magma crystallization ages of 242 ± 3 Ma for the Shuangpengxi pluton and ~244–242 Ma for the Xiekeng pluton. Geochemical and Sr–Nd–Hf isotopic compositions reveal that the magma of the Shuangpengxi granodiorite was derived from partial melting of crustal materials. The Xiekeng diorites can be divided into high-Al diorite and high-Mg diorite. Both of them resulted from partial melting of enriched lithospheric mantle, but their mantle source had been modified by previous slab-derived melt. The high-Al diorite was formed by fractional crystallization of olivine, pyroxene and/or preferential accumulation of plagioclase, and the high-Mg diorite was formed by fractional crystallization of olivine and/or preferential accumulation of pyroxene. The Xiekeng granodioritic porphyry was formed by mixing of crust-derived and mantle-derived melts. We propose that the Early Indosinian magmatism resulted from break-off of subducted oceanic slab after collision. The slab break-off model can well explain the linear distribution of the Early Indosinian plutons and rapid crustal uplift during the Middle Triassic in the West Qinling.     

Transition from calc-alkaline to potassium-rich magmatism in subduction environments: geochemical and Sr, Nd, Pb isotopic constraints from the island of Vulcano (Aeolian arc)

The problem of mantle metasomatism vs. crustal contamination in the genesis of arc magmas with different potassium contents has been investigated using new trace element and Sr–Nd–Pb isotopic data on the island of Vulcano, Aeolian arc. The analysed rocks range in age from 120 ka to the present day, and cover a compositional range from basalt to rhyolite of the high-K calc-alkaline (HKCA) to shoshonitic (SHO) and potassic (KS) series. Older Vulcano products (>30 ka) consist of HKCA–SHO rocks with SiO₂=48–56%. They show lower contents of K₂O, Rb and of several other incompatible trace element abundances and ratios than younger rocks with comparable degree of evolution. ⁸⁷Sr/⁸⁶Sr ranges from 0.70417 to 0.70504 and increases with decreasing MgO and compatible element contents. ²⁰⁶Pb/²⁰⁴Pb ratios display significant variations (19.31 to 19.76) and are positively correlated with MgO, ¹⁴³Nd/¹⁴⁴Nd (0.512532–0.512768), ²⁰⁷Pb/²⁰⁴Pb (15.66–15.71) and ²⁰⁸Pb/²⁰⁴Pb (39.21–39.49). Overall, geochemical and isotopic data suggest that the evolution of the older series was dominated by assimilation–fractional crystallisation (AFC) with an important role for continuous mixing with mafic liquids. Magmas erupted within the last 30 ka consist mostly of SHO and KS intermediate and acid rocks, with minor mafic products. Except for a few acid rocks, they display moderate isotopic variations (e.g. ⁸⁷Sr/⁸⁶Sr=0.70457–0.70484; ²⁰⁶Pb/²⁰⁴Pb=19.28–19.55, but ²⁰⁷Pb/²⁰⁴Pb=15.66–15.82), which suggest an evolution by fractional crystallisation, or in some cases by mixing, with little interaction with crustal material. The higher Sr isotopic ratios (⁸⁷Sr/⁸⁶Sr=0.70494–0.70587) of a few, low-volume, intermediate to acid rocks support differentiation by AFC at shallow depths for some magma batches. New radiogenic isotope data on the Aeolian islands of Alicudi and Stromboli, as well as new data for lamproites from central Italy, are also reported in order to discuss along-arc compositional variations and to evaluate the role of mantle metasomatism. Geochemical and petrological data demonstrate that the younger K-rich mafic magmas from Vulcano cannot be related to the older HKCA and SHO ones by intra-crustal evolutionary processes and point to a derivation from different mantle sources. The data from Alicudi and Stromboli suggest that, even though interaction between magma and wall rocks of the Calabrian basement during shallow level magma evolution was an important process locally, a similar interpretation can be extended to the entire Aeolian arc. Received: 27 September 1999 / Accepted: 24 May 2000     

Signatures of the source for the Emeishan flood basalts in the Ertan area： Pb isotope evidence

The Emeishan flood basalts can be divided into high-Ti (HT) basalt (Ti/Y>500) and low-Ti (LT) basalt (Ti/Y<500). Sr, Nd isotopic characteristics of the lavas indicate that the LT- and the HT-type magmas originated from distinct mantle sources and parental magmas. The LT-type magma was derived from a shallower lithospheric mantle, whereas the HT-type magma was derived from a deeper mantle source that may be possibly a mantle plume. However, few studies on the Emeishan flood basalts involved their Pb isotopes, especially the Ertan basalts. In this paper, the authors investigated basalt samples from the Ertan area in terms of Pb isotopes, in order to constrain the source of the Emeishan flood basalts. The ratios of 206Pb/204Pb (18.31–18.41), 207Pb/204Pb (15.55–15.56) and 208Pb/204Pb (38.81–38.94) are significantly higher than those of the depleted mantle, just lying between EM I and EM II. This indicates that the Emeishan HT basalts (in the Ertan area) are the result of mixing of EMI end-member and EMII end-member.     

Central European Cenozoic plume volcanism with OIB characteristics and indications of a lower mantle source

Average concentrations of incompatible elements and isotopes of radiogenic Sr, Nd and Pb in a 350 km long belt of Central European volcanics (CECV) resemble those in OIB in general and in OIB from the N Atlantic in particular. This similarity allows to infer comparable sources for CECV and OIB which might have been located in the lower mantle according to seismic tomography and chemistry, with the latter unlike a MORB source. The incompatible element contribution of lower mantle origin can be modelled from primitive mantle minus continental crust and upper mantle inventories. Alkali basaltic magmas from the modelled source are close in composition to CECV and OIB. The continental crust contains almost half of the silicate Earth's content of Rb, K, Pb, Ba, Th and U, which were mobilized to a major extent through dehydration of subducted ocean crust. Related losses from the lower mantle had to be replaced by deep subductions of oceanic lithosphere recognized from their isotopic imprint. From a balance based on Nd isotopes it can be concluded that average CECV contains 60% matter from residual primitive mantle and 40% from deeply subducted lithosphere (including some young upper mantle materials). Plume products from separate CECV regions developed, within 45 Ma, from rather depleted to more primitive isotopic signatures. Four periods of volcanism from Eocene to late Quaternary time are explained as four pulses of an almost stationary ultrafast plume uprise as modelled by Larsen and Yuen (1997). Magma production has increased from the first to the third pulse with the peak during Miocene time in the Vogelsberg region. The final pulse produced the Quaternary Eifel volcanoes. Tectonism from the Alpine orogen has probably triggered the synchronous volcanism of CECV, Massif Central etc. The European lithospheric plate has moved under the control of the opening Atlantic almost in an eastern direction with a velocity of 1 cm per year and has shifted extinct volcanoes off their source channels. Received: 10 July 1998 / Accepted: 10 February 1999     

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     

The Geochemistry of the Arabian Lithospheric Mantle--a Source for Intraplate Volcanism?

We present trace element and Sr–Nd–Hf–Pb isotopecompositions for clinopyroxenes from anhydrous spinel peridotiteand garnet ± spinel pyroxenite xenoliths of Pan-Africanlithospheric mantle from Jordan, including the first high-precisiondouble-spike Pb isotope measurements of mantle clinopyroxene.Clinopyroxenes from the peridotites are variably Th–U–LILE–LREEenriched and display prominent negative Nb, Zr and Ti anomalies.MREE–HREE abundances can generally be modelled as partialmelting residues of spinel lherzolite with primitive-mantle-likecomposition after extraction of 5–10% melt, whereas theenrichments in Th–U–LILE–LREE require a Pan-Africanor later metasomatic event. The large range of Nd, Sr, Pb andHf isotope ratios in both peridotites and pyroxenites (e.g.Nd 1·4–17·5; ²⁰⁶Pb/²⁰⁴Pb 17·2–20·4;Hf 0·6–164·6) encompasses compositionsmore radiogenic than mid-ocean ridge basalt (MORB), and Pb isotopescover almost the entire range of oceanic basalt values. Hf valuesare some of the highest ever recorded in mantle samples andare decoupled from Nd in the same samples. Marked correlationsbetween Sr–Nd–Pb isotopes, LILE–LREE enrichmentsand HFSE depletion suggest that the metasomatizing agent wasa carbonatitic-rich melt and isotopic data suggest that metasomatismmay have been related to Pan-African subduction. The metasomaticmelt permeated depleted upper mantle (<16 kbar) during Pan-Africansubduction at 600–900 Ma, and the variably metasomatizedmaterial was then incorporated into the Arabian lithosphericmantle. There is no evidence for recent metasomatism (<30Ma) related to the Afar plume like that postulated to have affectedsouthern Arabian lithospheric mantle. Hf isotopes in the mantleclinopyroxenes are unaffected by metasomatism, and even somestrongly overprinted lithologies record ancient (>1·2Ga) pre-metasomatic Lu–Hf signatures of the depleted uppermantle that was the protolith of the Arabian lithospheric mantle.The ‘resistance’ of the Lu–Hf isotopic systemto later metasomatic events resulted in the development of extremelyheterogeneous Hf isotopic signatures over time that are decoupledfrom other isotopic systems. No mantle sample in this studyexactly matches the chemical and isotopic signature of the sourceof Jordanian intraplate basalts. However, the xenolith compositionsare broadly similar to those of the source of Arabian intraplatebasalts, suggesting that the numerous Cenozoic intraplate volcanicfields throughout Arabia may be the product of melting uppermantle wedge material fertilized during Pan-African subductionand incorporated into the Arabian lithospheric mantle. We proposea model whereby the proto-Arabian lithospheric mantle underwenta major melting event in early Proterozoic–late Archeantimes (at the earliest at 1·2 Ga). Island-arc volcanismand major crust formation occurred during the Pan-African orogeny,which liberated fluids and possibly small-degree melts thatmigrated through the mantle creating zones of enrichment forcertain elements depending upon their compatibility. Immobileelements, such as Nb, were concentrated near the base of themantle wedge providing the source of the Nb-rich Jordanian volcanicrocks. More mobile elements, such as LILE and LREE, were transportedup through the mantle and fertilized the shallow mantle sourceof the Jordanian xenoliths. Following subduction, the mantlewedge became fossilized and preserved distinct enriched anddepleted zones. Lithospheric rifting in the Miocene triggeredpartial melting of spinel-facies mantle in the lower lithosphere,which mixed with deeper asthenospheric garnet-facies melts asrifting evolved. These melts entrained segments of variablycarbonatite-metasomatized shallow lithospheric mantle en routeto the surface. KEY WORDS: Arabian lithospheric mantle; Jordan; mantle xenoliths; Sr–Nd–Hf–Pb isotopes     

Source components of the Gran Canaria (Canary Islands) shield stage magmas: evidence from olivine composition and Sr–Nd–Pb isotopes

The Canary Island primitive basaltic magmas are thought to be derived from an HIMU-type upwelling mantle containing isotopically depleted (NMORB)-type component having interacted with an enriched (EM)-type component, the origin of which is still a subject of debate. We studied the relationships between Ni, Mn and Ca concentrations in olivine phenocrysts (85.6–90.0 mol.% Fo, 1,722–3,915 ppm Ni, 1,085–1,552 ppm Mn, 1,222–3,002 ppm Ca) from the most primitive subaerial and ODP Leg 157 high-silica (picritic to olivine basaltic) lavas with their bulk rock Sr–Nd–Pb isotope compositions (⁸⁷Sr/⁸⁶Sr = 0.70315–0.70331, ¹⁴³Nd/¹⁴⁴Nd = 0.51288–0.51292, ²⁰⁶Pb/²⁰⁴Pb = 19.55–19.93, ²⁰⁷Pb/²⁰⁴Pb = 15.60–15.63, ²⁰⁸Pb/²⁰⁴Pb = 39.31–39.69). Our data point toward the presence of both a peridotitic and a pyroxenitic component in the magma source. Using the model (Sobolev et al. in: Science 316:412–417, 2007) in which the reaction of Si-rich melts originated during partial melting of eclogite (a high pressure product of subducted oceanic crust) with ambient peridotitic mantle forms olivine-free reaction pyroxenite, we obtain an end member composition for peridotite with ⁸⁷Sr/⁸⁶Sr = 0.70337, ¹⁴³Nd/¹⁴⁴Nd = 0.51291, ²⁰⁶Pb/²⁰⁴Pb = 19.36, ²⁰⁷Pb/²⁰⁴Pb = 15.61 and ²⁰⁸Pb/²⁰⁴Pb = 39.07 (EM-type end member), and pyroxenite with ⁸⁷Sr/⁸⁶Sr = 0.70309, ¹⁴³Nd/¹⁴⁴Nd = 0.51289, ²⁰⁶Pb/²⁰⁴Pb = 20.03, ²⁰⁷Pb/²⁰⁴Pb = 15.62 and ²⁰⁸Pb/²⁰⁴Pb = 39.84 (HIMU-type end member). Mixing of melts from these end members in proportions ranging from 70% peridotite and 30% pyroxenite to 28% peridotite and 72% pyroxenite derived melt fractions can generate the compositions of the most primitive Gran Canaria shield stage lavas. Combining our results with those from the low-silica rocks from the western Canary Islands (Gurenko et al. EPSL 277:514–524, 2009), at least four distinct components are required. We propose that they are (1) HIMU-type pyroxenitic component (representing recycled ocean crust of intermediate age) from the plume center, (2) HIMU-type peridotitic component (ancient recycled ocean crust stirred into the ambient mantle) from the plume margin, (3) depleted, MORB-type pyroxenitic component (young recycled oceanic crust) in the upper mantle entrained by the plume, and (4) EM-type peridotitic component from the asthenosphere or lithosphere above the plume center.     

Tertiary--Quaternary Extension-Related Alkaline Magmatism in Western and Central Europe

Primitive mafic alkaline volcanic rocks from the Tertiary-Quaternaryextension-related magmatic province of western and central Europehave major and trace element and Sr–Nd–Pb isotopiccharacteristics which suggest the involvement of both lithosphericand asthenospheric mantle source components in their petrogenesis.Oxygen isotope data for the volcanic rocks, mantle xenoliths,and lower-crustal mafic xenoliths indicate that extensive crustalcontamination is not involved in the petrogenesis of these magmas. The geochemical characteristics of the lithospheric componentare in part constrained by those of spinel lherzolite and maficgranulite xenoliths entrained within the magmas. This componentappears to be the product of partial melting of phlogopite/amphibole-bearingmantle which was meta-somatized as a consequence of magmaticactivity during and preceding the Hercynian orogeny and duringphases of Permo-Carboniferous extension. Partial melting ofphlogopite is required to account for the generation, of potassicmagmas (leucitites and leucite nephelinites) with K₂O/Na₂O>1. This component appears to differ between the individual Hercynianterrane blocks of Europe, reflecting, in part, their previousmagmatic histories. The asthenospheric component has affinities with the sourceof St. Helena type (HIMU) OIB and may, in part, be 500–400 Ma recycled oceanic lithosphere subducted during the Hercynianorogeny. Alternatively, it could represent a zone of enrichedmantle at the base of the subcontinental lithosphere which ispreferentially partially melted during extension. There appearsto be no need to invoke the existence of deep mantle plumesto explain the HIMU characteristics, although the data do notpreclude them.     

Geochemistry and petrogenesis of volcanic rocks in the Kuril island arc

Newly obtained precise analytical data on trace elements and radiogenic Sr, Nd, and Pb isotopes testify to anomalous geochemical characteristics of mafic and intermediate Quaternary lavas in Paramushir (in the north of the Kuril arc), Kunashir and Iturup (in the south) islands, which are the largest three islands of the Kuril island arc. The high K and LREE concentrations in the volcanic products in Paramushir Island resulted from the southward expansion of the mantle thermal anomaly of the Kamchatka Peninsula and the involvement of melts related to the melting of oceanic sediments in magma generation. The depleted characteristics of the mafic volcanics are explained by the relatively young tectono-magmatic events during the opening of the Kuril backarc basin. The Kuril island-arc system developed on a heterogeneous basement. The northern islands are a continuation of the volcanic structures of southern Kamchatka, which were formed above an isotopically depleted and hot lithospheric mantle domain of composition close to that of the Pacific MORB type. The southern islands were produced above an isotopically enriched and cold lithospheric domain of the Indian-Ocean MORB type, which was modified in relation to relatively young backarc tectono-magmatic processes. Although issues related to the genesis of the transverse geochemical zoning were beyond the originally formulated scope of our research, the homogeneous enough isotopic composition of the rear-arc lavas in the absence of any mineralogical and geochemical lines of evidence of crustal contamination suggests an independent magmatic source.     

Petrogenesis of the Neogene alkaline volcanics with implications for post-collisional lithospheric thinning of the Eastern Pontides, NE Turkey

Whole-rock geochemistry, Sr–Nd–Pb isotopes and K–Ar data are reported for alkaline samples collected from the Neogene alkaline volcanics (NAVs) in the Eastern Pontides, northeastern Turkey, in order to investigate their source and petrogenesis and geodynamic evaluation of the region. The NAVs were made of three groups that comprise of basanite–tephrite (feldspar-free; Group A), tephrite–tephriphonolite (feldspar and feldspathoid-bearing; Group B) and alkaline basalt–rhyolite (feldspathoid-free; Group C) series. These rocks cover a broad compositional range from silica-undersaturated to silica-oversaturated types, almost all of which are potassic in character. They show enrichment of LREE and LILE and depletion of HFSE, without a Eu anomaly in most of the mafic samples. Textural features and calculated pressures based on the Cpx-barometer in each series indicate that the alkaline magma equilibrated at shallow crustal depths under a pressure of about 3–4.5 kbar and approximating a crystallization depth of 9–14 km. The NAVs are slightly depleted in isotopic composition, with respect to ⁸⁷Sr/⁸⁶Sr (ranging from 0.705018 to 0.705643) and ¹⁴³Nd/¹⁴⁴Nd (ranging from 0.512662 to 0.512714) that indicate young Nd model ages (0.51–059 Ga). This may indicate that the parent melts tapped a homogeneous and young lithospheric mantle source which was metasomatized by subduction-derived sediments during the Late Mesozoic. Pb isotopic compositions (²⁰⁶Pb/²⁰⁴Pb = 18.85–18.95; ²⁰⁷Pb/²⁰⁴Pb = 15.60–15.74; ²⁰⁸Pb/²⁰⁴Pb = 38.82–39.25) may also be consistent with a model for an enriched subcontinental lithospheric mantle source. Lithospheric thinning and resultant upwelling of asthenosphere induced by lithospheric delamination may have favoured partial melting of chemically enriched, young lithospheric mantle beneath the Eastern Pontides. Then, the melt subsequently underwent a fractional crystallization process along with or without minor amounts of crustal assimilation, generating a wide variety of rock types in a post-collision extensional regime in the Eastern Pontides during the Neogene.