Sr-Nd-Pb isotope ratios, geochemical compositions, and 40Ar/39Ar data of lavas from San Felix Island (Southeast Pacific): Implications for magma genesis and sources

We present the first trace element and age data combined with new Sr, Nd, and Pb isotope ratios on lavas from San Felix Island in the Southeast Pacific. A ⁴⁰Ar/³⁹Ar plateau age of 421 ± 18 ka implies young intraplate volcanic activity in this region relative to the ∼22 Ma old volcanism on the neighbouring Easter seamount chain (ESC). The incompatible element compositions of the San Felix magmas are similar to those of EM1-type basalts from Gough, although the isotopic compositions differ. San Felix formed some 20 Ma after the ESC plume affected the plate in this region but no chemical signature of the ESC material is observed in the young volcanic rocks. The composition of the San Felix basalts indicates a mantle source containing old continental lithospheric material from either metasomatized mantle or recycled sediments, which ascends in a weak mantle plume.     

Temporal evolution of the kerguelen plume: Geochemical evidence from 38 to 82 ma lavas forming the Ninetyeast ridge

Abstract Basaltic basement has been recovered by deep-sea drilling at seven sites on the linear Ninetyeast Ridge in the eastern Indian Ocean. Studies of the recovered lavas show that this ridge formed from ~ 82 to 38 Ma as a series of subaerial volcanoes that were created by the northward migration of the Indian Plate over a fixed magma source in the mantle. The Sr, Nd and Pb isotopic ratios of lavas from the Ninetyeast Ridge range widely, but they largely overlap with those of lavas from the Kerguelen Archipelago, thereby confirming previous inferences that the Kerguelen plume was an important magma source for the Ninetyeast Ridge. Particularly important are the ~ 81 Ma Ninetyeast Ridge lavas from DSDP Site 216 which has an anomalous subsidence history (Coffin 1992). These lavas are FeTi-rich tholeiitic basalts with isotopic ratios that overlap with those of highly alkalic, Upper Miocene lavas in the Kerguelen Archipelago. The isotopic characteristics of the latter which erupted in an intraplate setting have been proposed to be the purest expression of the Kerguelen plume (Weis et al. 1993a,b). Despite the overlap in isotopic ratios, there are important compositional differences between lavas erupted on the Ninetyeast Ridge and in the Kerguelen Archipelago. The Ninetyeast Ridge lavas are dominantly tholeiitic basalts with incompatible element abundance ratios, such as La/Yb and Zr/Nb, which are intermediate between those of Indian Ocean MORB (mid-ocean ridge basalt) and the transitional to alkalic basalts erupted in the Kerguelen Archipelago. These compositional differences reflect a much larger extent of melting for the Ninetyeast Ridge lavas, and the proximity of the plume to a spreading ridge axis. This tectonic setting contrasts with that of the recent alkalic lavas in the Kerguelen Archipelago which formed beneath the thick lithosphere of the Kerguelen Plateau. From ~ 82 to 38 Ma there was no simple, systematic temporal variation of Sr, Nd and Pb isotopic ratios in Ninetyeast Ridge lavas. Therefore all of the isotopic variability cannot be explained by aging of a compositionally uniform plume. Although Class et al. (1993) propose that some of the isotopic variations reflect such aging, we infer that most of the isotopic heterogeneity in lavas from the Ninetyeast Ridge and Kerguelen Archipelago can be explained by mixing of the Kerguelen plume with a depleted MORB-like mantle component. However, with this interpretation some of the youngest, 42–44 Ma, lavas from the southern Ninetyeast Ridge which have²⁰⁶pb/²⁰⁴Pb ratios exceeding those in Indian Ocean MORB and Kerguelen Archipelago lavas require a component with higher²⁰⁶Pb/²⁰⁴Pb, such as that expressed in lavas from St. Paul Island.     

Petrology and geochemistry of Camiguin Island, southern Philippines: insights to the source of adakites and other lavas in a complex arc setting

Camiguin is a small volcanic island located 12 km north of Mindanao Island in southern Philippines. The island consists of four volcanic centers which have erupted basaltic to rhyolitic calcalkaline lavas during the last ∼400 ka. Major element, trace element and Sr, Nd and Pb isotopic data indicate that the volcanic centers have produced a single lava series from a common mantle source. Modeling results indicate that Camiguin lavas were produced by periodic injection of a parental magma into shallow magma chambers allowing assimilation and fractional crystallization (AFC) processes to take place. The chemical and isotopic composition of Camiguin lavas bears strong resemblance to the majority of lavas from the central Mindanao volcanic field confirming that Camiguin is an extension of the tectonically complex Central Mindanao Arc (CMA). The most likely source of Camiguin and most CMA magmas is the mantle wedge metasomatized by fluids dehydrated from a subducted slab. Some Camiguin high-silica lavas are similar to high-silica lavas from Mindanao, which have been identified as “adakites” derived from direct melting of a subducted basaltic crust. More detailed comparison of Camiguin and Mindanao adakites with silicic slab-derived melts and magnesian andesites from the western Aleutians, southernmost Chile and Batan Island in northern Philippines indicates that the Mindanao adakites are not pure slab melts. Rather, the CMA adakites are similar to Camiguin high-silica lavas which are products of an AFC process and have negligible connection to melting of subducted basaltic crust. Received: 27 February 1998 / Accepted: 27 August 1998     

Geochemistry and petrology of lavas from the submarine flanks of Réunion Island (western Indian Ocean): implications for magma genesis and the mantle source

Summary Major and trace element data as well as Sr and Nd isotope compositions for submarine lavas from the flanks of Réunion island are reported. The submarine basalts of the island have major and trace element compositions similar to those of the subaerial basaltic rocks. This implies that no compositional change occurs in the shield-building magmas of the two Réunion volcanoes. Fractional crystallization of lavas from both Piton de la Fournaise and Piton des Neiges begin well within the mantle at pressures up to 1 GPa which is significantly deeper than the crust-mantle boundary at about 12 km depth. The Réunion primary magmas form at an average depth of about 4 GPa in agreement with the thickness of the plate beneath the island. Lavas from both Réunion volcanoes have similar trace element compositions with the exception of lower Th/Ba for Piton des Neiges which implies a relatively homogeneous plume source during, at least, the last 2 Ma. The lack of any variation in the partial melting processes during this time span implies a thermal steady state of the plume centre. The Réunion lavas form either from a source that was enriched by partial melting or that contains recycled enriched MORB. Based on MORB- like Ce/Pb and Nb/U ratios an influence by fluid-metasomatized mantle, sediment or continental crustal material in the Réunion source appears unlikely. Received August 15, 2000; revised version accepted June 21, 2001     

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     

The Transition to Potassic Alkaline Volcanism in Island Arcs: The Ringgit--Beser Complex, East Java, Indonesia

The origin of potassic lavas with within-plate characteristicsin island are settings is unclear. The volcanic complex of Ringgit—Beser,situated in eastern Java, has erupted lavas of both normal islandare calc-alkaline type and atypical potassic lavas, includingsome highly magnesian lavas. The occurrence of these primitivelavas gives an unusual insight into the source characteristicsof the potassic lavas. The lavas from Ringgit—Beser have a wide range of K₂O(1.1–6.4 wt. %) and MgO contents (18.0–1.6 wt.%).The most magnesian lavas have high Ni and Cr contents. The calc-alkalinelavas have incompatible trace element patterns typical of islandare lavas with enrichments in large ion lithophile elements(LILE) and light rare earth elements (LREE) relative to highfield strength elements (HFSE) and heavy REE (HREE). The potassiclavas may be divided into two series on the basis of Ba andNb contents, with the enriched potassic (EK) series having higherBa and Nb contents for a given MgO content than the potassic(K) series. The EK and K series lavas have some incompatibletrace element ratios similar to within-plate lavas (e.g., highCe/Pb, low LILE/HFSE ratios, and low B/Be). However, both theEK series and K series lavas have negative Ti and Zr anomalies,and the EK series lavas have high Ba/La similar to are lavas.There is little distinction in Sr and Nd isotopes between theK and EK series, but the calc-alkaline lavas have lower ₈₇Sr/₈₆Srand higher ₁₄₃Nd/₁₄₄Nd ratios than the potassic lavas. The EKseries lavas have lower ₂₀₆Pb/₂₀₄Pb and higher ₂₀₈Pb/₂₀₄Pb thanthe K series lavas, but similar ₂₀₇Pb/₂₀₄Pb ratios. The K serieslavas define an almost horizontal trend in ₂₀₇Pb–₂₀₆Pbspace. The Pb isotopic ratios indicate that the EK series lavasare derived from a single mantle source, whereas the K seriesoriginate from a mixture of two mantle components. Calc-alkalinelavas have Pb isotope ratios similar to other calc-alkalineand tholeiitic lavas from Java, and plot on a mixing line betweenIndian Ocean mid-ocean ridge basalt (MORB) and Indian Oceansediment. Incompatible trace element and Pb isotope data for the calc-alkalinelavas indicate that these lavas have a similar source to othercalc-alkaline lavas erupted in Java, namely melts of the IndianOcean MORB mantle fluxed by fluids from the subducted slab.The potassic lavas originate from enriched mantle sources withinthe wedge which have not been affected by recent subductionprocesses. The EK series lavas are derived from a metasomatizedzone which has EMI-type characteristics. The K series lavasare derived from mixing of melts from Christmas Island-type(EMII) mantle and the metasomatized zone. The metasomatizedzone is probably situated at the base of the lithosphere andthe Indian Ocean MORB and Christmas Island-type mantle componentsare situated in the asthenosphere of the wedge. Isotopic datafor Ringgit—Beser lavas confirm that the mantle wedgeof the Sunda arc is extremely heterogeneous (Foden & Varne,1980; Varne, 1985; Wheller et al., 1987). The similarity in geochemistry between Indonesian potassic lavasand those erupted in continental settings indicates that themagma source is essentially the same, namely a metasomatizedphlogopite-rich layer generated by melts of recycled subductedlithosphere. The lack of negative Ti anomalies in the continentalpotassic lavas is ascribed to lower oxidation states in themantle in continental settings.     

Controls on magmatism in an island arc environment: study of lavas and sub-arc xenoliths from the Tabar–Lihir–Tanga–Feni island chain, Papua New Guinea

The Tabar–Lihir–Tanga–Feni (TLTF) islands of Papua New Guinea mainly comprise high-K calc-alkaline and silica undersaturated alkaline rocks that have geochemical features typical for subduction-related magmatism. Numerous sedimentary, mafic, and ultramafic xenoliths recovered from Tubaf seamount, located on the flank of Lihir Island, provide a unique opportunity to study the elemental and isotopic composition of the crust and mantle wedge beneath the arc and to evaluate their relationships to the arc magmatism in the region. The sedimentary and mafic xenoliths show that the crust under the islands is composed of sedimentary sequences and oceanic crust with Pacific affinity. A majority of the ultramafic xenoliths contain features indicating wide spread metasomatism in the mantle wedge under the TLTF arc. Leaching experiments reveal that the metasomatized ultramafic xenoliths contain discrete labile phases that can account for up to 50% or more of elements such as Cu, Zn, Rb, U, Pb, and light REE (rare-earth elements), most likely introduced in the xenoliths via hydrous fluids released from a subducted slab. The leaching experiments demonstrated that the light REE enrichment pattern can be more or less removed from the metasomatized xenoliths and the residual phases exhibit REE patterns that range from flat to light REE depleted. Sr–Nd isotopic data for the ultramafic residues show a coupled behavior of increasing ⁸⁷Sr/⁸⁶Sr with decreasing ¹⁴³Nd/¹⁴⁴Nd ratios. The labile phases in the ultramafic xenoliths, represented by the leachates, show decoupling between Sr and Nd with distinctly more radiogenic ⁸⁷Sr/⁸⁶Sr than the residues. Both leachates and residues exhibit very wide range in their Pb isotopic compositions, indicating the involvement of three components in the mantle wedge under the TLTF islands. Two of the components can be identified as Pacific Oceanic mantle and Pacific sediments. Some of the ultramafic samples and clinopyroxene separates, however, exhibit relatively low ²⁰⁶Pb/²⁰⁴Pb at elevated ²⁰⁷Pb/²⁰⁴Pb suggesting that the third component is either Indian Ocean-type mantle or Australian subcontinental lithospheric mantle. Geochemical data from the ultramafic xenoliths indicate that although the mantle wedge in the area was extensively metasomatized, it did not significantly contribute to the isotopic and incompatible trace element compositions of TLTF lavas. Compared to the mantle samples, the TLTF lavas have very restricted Pb isotopic compositions that lie within the Pacific MORB range, indicating that magma compositions were dominated by melts released from a stalled subducted slab with Pacific MORB affinity. Interaction of slab melts with depleted peridotitic component in the mantle wedge, followed by crystal fractionation most likely generated the geochemical characteristics of the lavas in the area. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Geochemistry and geochronology of the mafic lavas from the southeastern Ethiopian rift (the East African Rift System): assessment of models on magma sources,plume–lithosphere interaction and plume evolution

Major and trace element and isotopic ratios (Sr, Nd and Pb) are presented for mafic lavas (MgO > 4 wt%) from the southwestern Yabello region (southern Ethiopia) in the vicinity of the East African Rift System (EARS). New K/Ar dating results confirm three magmatic periods of activity in the region: (1) Miocene (12.3–10.5 Ma) alkali basalts and hawaiites, (2) Pliocene (4.7–3.6 Ma) tholeiitic basalts, and (3) Recent (1.9–0.3 Ma) basanite-dominant alkaline lavas. Trace element and isotopic characteristics of the Miocene and Quaternary lavas bear a close similarity to ocean island basalts that derived from HIMU-type sublithospheric source. The Pliocene basalts have higher Ba/Nb, La/Nb, Zr/Nb and ⁸⁷Sr/⁸⁶Sr (0.70395–0.70417) and less radiogenic Pb isotopic ratios (²⁰⁶Pb/²⁰⁴Pb = 18.12–18.27) relative to the Miocene and Quaternary lavas, indicative of significant contribution from enriched subcontinental lithospheric mantle in their sources. Intermittent upwelling of hot mantle plume in at least two cycles can explain the magmatic evolution in the southern Ethiopian region. Although plumes have been originated from a common and deeper superplume extending from the core–mantle boundary, the diversity of plume components during the Miocene and Quaternary reflects heterogeneity of secondary plumes at shallower levels connected to the African superplume, which have evolved to more homogeneous source.     

Geochemistry of southern Pagan Island lavas,Mariana arc: the role of subduction zone processes

New major and trace element abundances, and Pb, Sr, and Nd isotopic ratios of Quaternary lavas from two adjacent volcanoes (South Pagan and the Central Volcanic Region, or CVR) located on Pagan Island allow us to investigate the mantle source (i.e., slab components) and melting dynamics within the Mariana intra-oceanic arc. Geologic mapping reveals a pre-caldera (780–9.4 ka) and post-caldera (<9.4 ka) eruptive stage for South Pagan, whereas the eruptive history of the older CVR is poorly constrained. Crystal fractionation and magma mixing were important crustal processes for lavas from both volcanoes. Geochemical and isotopic variations indicate that South Pagan and CVR lavas, and lavas from the northern volcano on the island, Mt. Pagan, originated from compositionally distinct parental magmas due to variations in slab contributions (sediment and aqueous fluid) to the mantle wedge and the extent of mantle partial melting. A mixing model based on Pb and Nd isotopic ratios suggests that the average amount of sediment in the source of CVR (~2.1%) and South Pagan (~1.8%) lavas is slightly higher than Mt. Pagan (~1.4%) lavas. These estimates span the range of sediment-poor Guguan (~1.3%) and sediment-rich Agrigan (~2.0%) lavas for the Mariana arc. Melt modeling demonstrates that the saucer-shaped normalized rare earth element (REE) patterns observed in Pagan lavas can arise from partial melting of a mixed source of depleted mantle and enriched sediment, and do not require amphibole interaction or fractionation to depress the middle REE abundances of the lavas. The modeled degree of mantle partial melting for Agrigan (2–5%), Pagan (3–7%), and Guguan (9–15%) lavas correlates with indicators of fluid addition (e.g., Ba/Th). This relationship suggests that the fluid flux to the mantle wedge is the dominant control on the extent of partial melting beneath Mariana arc volcanoes. A decrease in the amount of fluid addition (lower Ba/Th) and extent of melting (higher Sm/Yb), and an increase in the sediment contribution (higher Th/Nb, La/Sm, and Pb isotopic ratios) from Mt. Pagan to South Pagan could reflect systematic cross-arc or irregular along-arc melting variations. These observations indicate that the length scale of compositional heterogeneity in the mantle wedge beneath Mariana arc volcanoes is small (~10 km).     

Osmium isotope systematics of historical lavas from Piton de la Fournaise (Réunion Island, Indian Ocean)

Re–Os isotope and elemental data have been obtained for 20 historical picrites and basalts (1931–2006) from the Piton de la Fournaise volcano on Réunion Island and two old (>0.78?Ma) cumulates from a drill hole in the eastern part of the volcano. The ¹⁸⁷Os/¹⁸⁸Os ratios of the historical lava samples, selected to cover the MgO concentration and Pb isotopic ranges of Piton de la Fournaise lavas, range from 0.1311 to 0.1374. This result, together with previous results on 66-Ma-old lavas from the Deccan Traps (Allègre et al. in. Earth Planet Sci Lett, 170:197–204, 1999), supports the idea that the Os isotopic signature of the Réunion plume is relatively uniform and is at the less radiogenic end of the ocean island basalt spectrum. In detail, lavas erupted before 1992 seem to have higher ¹⁸⁷Os/¹⁸⁸Os than the lavas erupted after the 1992–1998 period of quiescence. Comparison of ¹⁸⁷Os/¹⁸⁸Os ratios with Pb, Sr and Nd isotopic data on the same set of samples shows no correlation between Os and Sr–Nd isotopes, whereas a broad positive relationship with Pb isotopes is observed, which is interpreted to reflect coupled fractionation of Re/Os and U–Th/Pb in the mantle due to the partitioning of Pb and Os into sulphides. Lavas inferred to be recording the Os isotopic signature of the Réunion plume source have higher ¹⁸⁷Os/¹⁸⁸Os ratios than the primitive mantle values. While this might be ascribed to melting of a lithologically heterogeneous source comprising recycled oceanic crust and/or continental sediment, the expected coupled Os–Sr–Nd–Pb isotopic variations are not observed. It is thus proposed that the mantle source for Piton de la Fournaise has inherently slightly radiogenic ¹⁸⁷Os/¹⁸⁸Os values that could reflect a mantle domain almost isolated from recycling processes.     

Petrogenesis of isotopically unusual Pliocene olivine leucitites from Deep Springs Valley, California

High-K mafic alkalic lavas (5.4 to 3.2 wt% K₂O) from Deep Springs Valley, California define good correlations of increasing incompatible element (e.g., Sr, Zr, Ba, LREE) and compatible element contents (e.g., Ni, Cr) with increasing MgO. Strontium and Nd isotope compositions are also correlated with MgO; ⁸⁷Sr/⁸⁶Sr ratios decrease and ɛ_Nd values increase with decreasing MgO. The Sr and Nd isotope compositions of these lavas are extreme compared to most other continental and oceanic rocks; ⁸⁷Sr/⁸⁶Sr ratios range from 0.7121 to 0.7105 and ɛ_Nd values range from −16.9 to −15.4. Lead isotope ratios are relatively constant, ²⁰⁶Pb/²⁰⁴Pb ∼17.2, ²⁰⁷Pb/²⁰⁴Pb ∼15.5, and ²⁰⁸Pb/²⁰⁴Pb ∼38.6. Depleted mantle model ages calculated using Sr and Nd isotopes imply that the reservoir these lavas were derived from has been distinct from the depleted mantle reservoir since the early Proterozoic. The Sr-Nd-Pb isotope variations of the Deep Springs Valley lavas are unique because they do not plot along either the EM I or EM II arrays. For example, most basalts that have low ɛ_Nd values and unradiogenic ²⁰⁶Pb/²⁰⁴Pb ratios have relatively low ⁸⁷Sr/⁸⁶Sr ratios (the EM I array), whereas basalts with low ɛ_Nd values and high ⁸⁷Sr/⁸⁶Sr ratios have radiogenic ²⁰⁶Pb/²⁰⁴Pb ratios (the EM II array). High-K lavas from Deep Springs Valley have EM II-like Sr and Nd isotope compositions, but EM I-like Pb isotope compositions. A simple method for producing the range of isotopic and major- and trace-element variations in the Deep Springs Valley lavas is by two-component mixing between this unusual K-rich mantle source and a more typical depleted mantle basalt. We favor passage of MORB-like magmas that partially fused and were contaminated by potassic magmas derived from melting high-K mantle veins that were stored in the lithospheric mantle. The origin of the anomalously high ⁸⁷Sr/⁸⁶Sr and ²⁰⁸Pb/²⁰⁴Pb ratios and low ɛ_Nd values and ²⁰⁶Pb/²⁰⁴Pb ratios requires addition of an old component with high Rb/Sr and Th/Pb ratios but low Sm/Nd and U/Pb ratios into the mantle source region from which these basalts were derived. This old component may be sediments that were introduced into the mantle, either during Proterozoic subduction, or by foundering of Proterozoic age crust into the mantle at some time prior to eruption of the lavas. Received: 28 February 1997 / Accepted: 9 July 1998     

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     

Geochemistry of Heard Island (Southern Indian Ocean): Characterization of an Enriched Mantle Component and Implications for Enrichment of the Sub-Indian Ocean Mantle

Lavas from Heard Island, located on the Kerguelen Plateau inthe southern Indian Ocean, exhibit the largest range (e.g.,⁸⁷Sr/⁸⁶Sr=0.7047–0.7079) of isotopic compositions yetobserved on a single oceanic island. Isotopic compositions arewell correlated and are accompanied by systematic changes inincompatible trace element ratios, particularly those involvingNb. These variations are interpreted as resulting from mixingbetween two components. One is characterized by high ⁸⁷Sr/⁸⁶Sr,low ²⁰⁶Pb/²⁰⁴Pb and ¹⁴³Nd/¹⁴⁴Nd ratios, and negative Nb andEu anomalies, and is derived ultimately from the upper continentalcrust. The other has lower ⁸⁷Sr/⁸⁶Sr, and higher ²⁰⁶Pb/²⁰⁴Pband ¹⁴³Nd/¹⁴⁴Nd ratios, and lacks the depletions in Nb and Eu.Two possible compositions are considered for the low-⁸⁷Sr/⁸⁶Srcomponent of the source. The first is at the low-⁸⁷Sr/⁸⁶Sr endof the Heard Island data array, represented most closely bylavas from the Laurens Peninsula. However, trace element variationssuggest that these lavas might not be representive of the Heardplume. The second is close to the low-⁸⁷Sr/⁸⁶Sr end of the isotopicarray for lavas from the main volcano. In this case a lithosphericmantle origin is suggested for the Laurens Peninsula lavas.The relationships between isotopic data, major element compositions,and incompatible trace element ratios indicate that the continent-derivedmaterial is probably present in the mantle source, where itmakes a maximum contribution of <4 wt.% for all but one HeardIsland sample. However, if the Kerguelen Plateau is a submergedcontinental block, shallow-level contamination cannot be ruledout. The binary mixing model developed to explain the Heard Islandgeochemical variations is extended to include other Indian Oceanoceanic island and mid-ocean ridge basalts (OIB and MORB). Weshow that isotopic compositions of Indian Ocean OIB are consistentwith sampling of a regional reservoir in which the same twocomponents exist in variable proportions (generally 1–5wt.% of the continent-derived component). The distinctive isotopiccompositions of Indian Ocean MORB are consistent with mixingof a similar component into an Atlantic-or Pacific-like MORBmantle source. The relatively unradiogenic ²⁰⁶Pb/²⁰⁴Pb isotopiccompositions of these ‘enriched’ Indian Ocean mantlecomponents are unlike any present-day marine sediments and indicatethat their source has had ²³⁸U/²⁰⁴Pb ratios (µ) much lowerthan typical upper continental crust for > 1 Ga. These agespre-date the formation of Gondwana (600-130 Ma) and thereforedo not support sediment subduction beneath Gondwana as the causeof enrichment in the sub-Indian Ocean mantle. We propose thatthe enrichment of Indian Ocean OIB sources was due to subductionof upper-crustal material beneath a Proterozoic precursor ofGondwana at 1–2 Ga. The enrichment of the Indian OceanMORB sources could have had a similar origin, or could havebeen derived from sub-continental lithospheric mantle returnedto the asthenospheric mantle, perhaps during the break-up ofGondwana (200–130 Ma).     

A Pb isotope investigation of the Guli massif, Maymecha-Kotuy alkaline-ultramafic complex, Siberian flood basalt province, Polar Siberia

Summary Covering a vast area of the northern Siberian platform are the Siberian flood basalts (SFB), which make up one of the world’s largest magmatic provinces. Along the northeastern margin of the SFB province lies the Maymecha-Kotuy alkaline-ultramafic complex, consisting of a large volume of alkaline lavas, numerous dykes, and the Guli massif together with numerous other, smaller alkaline plutons. The genetic link between the SFB and the Maymecha-Kotuy complex continues to be a subject of active debate. Although the rocks in both units have essentially the same age close to the Permian-Triassic boundary, questions remain as to the relative order of emplacement and the contributing source materials of each lithology. This study builds upon earlier petrologic, geochemical, and isotopic work to further an understanding of the relationship between SFB and alkaline rocks. A whole-rock U-Pb age of 250 ± 9 Ma was determined for the Guli massif, which lies within the range of ages previously reported for the SFB. The Pb isotopic composition of the Guli rocks plot mainly in the lower portion of the OIB field, and dunite and carbonatite extend downward into the MORB field suggesting for them a more depleted source than the one that produced the SFB. The combined Pb, Sr, and Nd isotopic systematics of the SFB and the Guli alkaline rocks enable the identification of several discrete source components. The first component dominates many of the Guli rocks and is characterized by low ⁸⁷Sr/⁸⁶Sr (0.7031 to 0.7038), high ε_Nd (+5.35 to +3.97), and relatively unradiogenic Pb (²⁰⁶Pb/²⁰⁴Pb = 17.88–18.31; ²⁰⁷Pb/²⁰⁴Pb = 15.38–15.46; ²⁰⁸Pb/²⁰⁴Pb = 37.33–37.70), which we associate with the depleted (MORB source) mantle. The second component representing most of the SFB demonstrates a notable chemical and isotopic uniformity with ⁸⁷Sr/⁸⁶Sr values of 0.7046 to 0.7052, ε_Nd values of 0 to +2.5, and an average Pb isotopic composition of ²⁰⁶Pb/²⁰⁴Pb = 18.3, ²⁰⁷Pb/²⁰⁴Pb = 15.5, and ²⁰⁸Pb/²⁰⁴Pb = 38.0. This component, making up the majority of SFB, is speculated to be a relatively primitive lower mantle plume with a near-chondritic signature. Contamination by upper and lower continental crustal material, designated as components 3 and 4, is postulated to explain the isotopic characteristics of some of the higher SiO₂ Guli rocks and SFB. Finally, metasomatic processes associated with the invasion of the Siberian super-plume add a fifth component responsible for the extreme enrichment in rare-earth and related elements found in some Guli rocks and SFB.     

Changing compositions in the Iceland plume; Isotopic and elemental constraints from the Paleogene Faroe flood basalts

Elemental and Sr, Nd, Hf and high precision Pb isotopic data are presented from 59 low-Ti and high-Ti lavas from the syn-break up part of the Faroe Flood Basalt Province. The depleted MORB-like low-Ti lavas erupted in the rift zone between the Faroe Islands and central East Greenland around the time of break up of the North Atlantic have isotopic end-member compositions different from the depleted Iceland lavas. We suggest that the main low-Ti mantle component is NAEM (North Atlantic End-Member (Ellam and Stuart, 2000, J. Petrol. 41, 919) and that the ²⁰⁷Pb/²⁰⁴Pb value of the component should be 15.35 and ε_Hf = + 16.5. NAEM is the main depleted component in the early Iceland plume. This is supported by high mantle potential temperatures (up to 1550 °C) calculated for the source of the low-Ti basalts. The unique mantle isotopic composition of NAEM with low ²⁰⁶Pb/²⁰⁴Pb (17.5) and Δ7/4Pb (? 3.8) precludes a derivation from recycled MORB lithosphere. Instead we suggest that NAEM represents a plume component of recycled depleted Archean lithospheric mantle that was further depleted ~ 500 Ma ago, possibly in connection with the recycling process. Two other isotopic end-members are required to explain the variation of the Faroe low-Ti basalts: (1) The Faroe depleted component (FDC), with ⁸⁷Sr/⁸⁶Sr = 0.7025, ε_Nd = + 11, ε_Hf = + 19.5, ²⁰⁶Pb/²⁰⁴Pb = 18.2, ²⁰⁷Pb/²⁰⁴Pb = 15.454 and ²⁰⁸Pb/²⁰⁴Pb = 37.75, which is similar in composition to some Atlantic MORB and is regarded as a local upper mantle source. (2) An enriched EM-type component similar in geochemistry to the Icelandic Öræfajökull lavas. This component is believed to be recycled pelagic sediments in the plume but it can alternatively be a local crustal or lithospheric mantle component. The enriched Faroe high-Ti lavas erupted inland from the rift have isotopic compositions very similar to the enriched Icelandic neo-volcanics and these lava suites apparently share the two enriched plume end-members IE1 and IE2 (Geochim. Cosmochim. Acta 68, 2, 2004). The lack of mixing between high and low-Ti melts at the time of break up, is explained by a zoned plume where only low-Ti sources were present beneath the rift zone surrounded by high-Ti sources on both sides of the rift. The enriched plume components in the high-Ti lava sequences on the Faroe Islands and central East Greenland changed rapidly on a ka-scale which implies, from geophysical modelling, that this area was positioned above the center of the plume, and that the Iceland plume was centered under the Atlantic ridge already from the Paleocene.     

Petrology and geochemistry of South Mid-Atlantic Ridge (19°S) lava flows: Implications for magmatic processes and possible plume-ridge interactions

The South Mid-Atlantic Ridge (SMAR) 19°S segment, approximately located along the line of Saint Helena volcanic chain (created by Saint Helena mantle plume), is an ideal place to investigate the issue whether the ridge-hotpot interaction process affected the whole MAR. In this study, we present major and trace elemental compositions and Sr-Nd-Pb isotopic ratios of twenty fresh lava samples concentrated in a relatively small area in the SMAR 19°S segment. Major oxides compositions show that all samples are tholeiite. Low contents of compatible trace elements (e.g., Ni ​= ​239–594 ​ppm and Cr ​= ​456–1010 ​ppm) and low Fe/Mn (54–67) and Ce/Yb (0.65–1.5) ratios of these lavas show that their parental magmas are partially melted by a spinel lherzolite mantle source. Using software PRIMELT3, this study obtained mantle potential temperatures (T_p) beneath the segment of 1321–1348 ​°C, which is lower relative to those ridges influenced by mantle plumes. The asthenospheric mantle beneath the SMAR 19°S segment starts melting at a depth of ~63 ​km and ceases melting at ~43 ​km with a final melting temperature of ~1265 ​°C. The extent of partial melting is up to 16%–17.6% with an average adiabatic decompression value of 2.6%/kbar. The correlations of major oxides (CaO/Al₂O₃) and trace elements (Cr, Co, V) with MgO and Zr show that the parental magma experienced olivine and plagioclase fractional crystallization during its ascent to the surface.⁸⁷Sr/⁸⁶Sr (0.702398–0.702996), ¹⁴³Nd/¹⁴⁴Nd (0.513017–0.513177) and ²⁰⁶Pb/²⁰⁴Pb (18.444–19.477) ratios of these lavas indicate the mantle source beneath the SMAR 19°S segment is composed of a three-component mixture of depleted MORB mantle, PREMA mantle, and HIMU mantle materials. The simple, binary mixing results among components from plume-free SMAR MORB, Saint Helena plume and Tristan plume show that asthenospheric mantle beneath the SMAR 19°S segment may be polluted by both Saint Helena and Tristan plume enriched materials. The abovementioned mantle potential temperatures, together with the low Saint Helena (<10%) and Tristan (<5%) components remaining in the asthenospheric mantle at present, show that the physically ridge-hotspot interactions at SMAR 19°S segment may have ceased. However, the trace element and Sr-Nd-Pb isotopically binary mixing calculation results imply that these lavas tapped some enriched pockets left when Saint Helena and/or Tristan plume were once on the SMAR during earlier Atlantic rifted history.     

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.     

Mantle-melt Evolution (Dynamic Source) in the Origin of a Single MORB Suite: a Perspective from Magnesian Glasses of Macquarie Island

The effects of source composition and source evolution duringprogressive partial melting on the chemistry of mantle-derivedmid-ocean ridge basalt (MORB) melts were tested using a comprehensivegeochemical and Sr–Nd–Pb isotopic dataset for fresh,magnesian basaltic glasses from the Miocene Macquarie Islandophiolite, SW Pacific. These glasses: (1) exhibit clear parent–daughterrelationships; (2) allow simple reconstruction of primary meltcompositions; (3) show exceptional compositional diversity (e.g.K₂O/TiO₂ 0·09–0·9; La/Yb 1·5–22;²⁰⁶Pb/²⁰⁴Pb 18·70–19·52); (4) preserve changesin major element and isotope compositions, which are correlatedwith the degree of trace element enrichment (e.g. La/Sm). Conventionalmodels for MORB genesis invoke melting of mantle that is heterogeneouson a small scale, followed by binary mixing of variably lithophileelement-enriched melt batches. This type of model fails to explainthe compositions of the Macquarie Island glasses, principallybecause incompatible element ratios (e.g. Nb/U, Sr/Nd) and Pbisotope ratios vary non-systematically with the degree of enrichment.We propose that individual melt batches are produced from instantaneous‘parental’ mantle parageneses, which change continuouslyas melting and melt extraction proceeds. This concept of a ‘dynamicsource’ combines the models of small-scale mantle heterogeneitiesand fractional melting. A dynamic source is an assemblage oflocally equilibrated mantle solids and a related melt fraction.Common MORB magmas that integrate the characteristics of numerousmelt batches therefore tend to conceal the chemical and isotopicidentity of a dynamic source. This study shows that isotoperatios of poorly mixed MORB melts are a complex function ofthe dynamic source evolution, and that the range in isotoperatios within a single MORB suite does not necessarily requiremixing of diverse components. KEY WORDS: mid-ocean ridge basalt; Macquarie Island; radiogenic isotopes; mantle; geochemistry     

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     

Isotopic and trace element constraints on the petrogenesis of lavas from the Mount Adams volcanic field,Washington

Strontium, Nd, Pb, Hf, Os, and O isotope compositions for 30 Quaternary lava flows from the Mount Adams stratovolcano and its basaltic periphery in the Cascade arc, southern Washington, USA indicate a major component from intraplate mantle sources, a relatively small subduction component, and interaction with young mafic crust at depth. Major- and trace-element patterns for Mount Adams lavas are distinct from the rear-arc Simcoe volcanic field and other nearby volcanic centers in the Cascade arc such as Mount St. Helens. Radiogenic isotope (Sr, Nd, Pb, and Hf) compositions do not correlate with geochemical indicators of slab-fluids such as (Sr/P) _n and Ba/Nb. Mass-balance modeling calculations, coupled with trace-element and isotopic data, indicate that although the mantle source for the calc-alkaline Adams basalts has been modified with a fluid derived from subducted sediment, the extent of modification is significantly less than what is documented in the southern Cascades. The isotopic and trace-element compositions of most Mount Adams lavas require the presence of enriched and depleted mantle sources, and based on volume-weighted chemical and isotopic compositions for Mount Adams lavas through time, an intraplate mantle source contributed the major magmatic mass of the system. Generation of basaltic andesites to dacites at Mount Adams occurred by assimilation and fractional crystallization in the lower crust, but wholesale crustal melting did not occur. Most lavas have Tb/Yb ratios that are significantly higher than those of MORB, which is consistent with partial melting of the mantle in the presence of residual garnet. δ ¹⁸O values for olivine phenocrysts in Mount Adams lavas are within the range of typical upper mantle peridotites, precluding involvement of upper crustal sedimentary material or accreted terrane during magma ascent. The restricted Nd and Hf isotope compositions of Mount Adams lavas indicate that these isotope systems are insensitive to crustal interaction in this juvenile arc, in stark contrast to Os isotopes, which are highly sensitive to interaction with young, mafic material in the lower crust.