Pb,Hf and Nd isotope compositions of the two Réunion volcanoes (Indian Ocean): A tale of two small-scale mantle “blobs”?

Pb, Hf, Nd and Sr isotopes of basaltic lavas from the two Réunion Island volcanoes are reported in order to examine the origin of the sources feeding these volcanoes and to detect possible changes through time. Samples, chosen to cover the whole lifetime of the two volcanoes (from 2 Ma to present), yield a chemically restricted (compared to OIB lavas) but complex distribution. Réunion plume isotopic characteristics have been defined on the basis of the composition of uncontaminated shield-building lavas from the Piton de la Fournaise volcano. The average ?_Nd, ?_Hf, ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb isotope ratios calculated for this component are + 4.4, + 9.1, 0.70411, 18.97, 15.59 and 39.03, respectively. In Pb–Pb isotope space, each volcano defines a distinct linear trend but slight variations are also detected within the various volcanic sequences. The Piton des Neiges volcano yields a distinct and significantly more scattered isotopic distribution than Piton de la Fournaise for both Pb, Hf and Nd isotope tracers. A principal component analysis of the Pb isotope data from Piton de la Fournaise reveals a major contribution of the C and EM-1 components (with a clear Dupal flavor) as main components for the modern Réunion plume. The same components have been identified for Piton des Neiges but with a stronger participation of a depleted mantle component and a weaker EM-1 contribution. The compositional change of the lavas erupted by the Piton des Neiges and Piton de la Fournaise volcanoes is attributed to the impingement of two small-scale blobs of plume material at the base of the Réunion lithosphere. Compared to other hot-spots worldwide, in particular Hawaii and Kerguelen, magmas beneath Réunion are generated from a considerably more homogeneous, compositionally more primitive plume higher in ²⁰⁶Pb. Although shallow-level contamination processes have been locally detected they did not alter significantly the composition of the plume magmas. This is tentatively attributed to mantle dynamics producing small, high-velocity blobs that ascend rapidly through the lithosphere, and to the lack of a well-developed magma chamber at depth in the lithosphere.     

<Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar dating of the eruptive history of Mount Erebus,Antarctica: volcano evolution

Mt. Erebus, a 3,794-meter-high active polygenetic stratovolcano, is composed of voluminous anorthoclase-phyric tephriphonolite and phonolite lavas overlying unknown volumes of poorly exposed, less differentiated lavas. The older basanite to phonotephrite lavas crop out on Fang Ridge, an eroded remnant of a proto-Erebus volcano and at other isolated locations on the flanks of the Mt. Erebus edifice. Anorthoclase feldspars in the phonolitic lavas are large (~10 cm), abundant (~30–40%) and contain numerous melt inclusions. Although excess argon is known to exist within the melt inclusions, rigorous sample preparation was used to remove the majority of the contaminant. Twenty-five sample sites were dated by the ⁴⁰Ar/³⁹Ar method (using 20 anorthoclase, 5 plagioclase and 9 groundmass concentrates) to examine the eruptive history of the volcano. Cape Barne, the oldest site, is 1,311±16 ka and represents the first of three stages of eruptive activity on the Mt. Erebus edifice. It shows a transition from sub-aqueous to sub-aerial volcanism that may mark the initiation of proto-Erebus eruptive activity. It is inferred that a further ~300 ky of basanitic/phonotephritic volcanism built a low, broad platform shield volcano. Cessation of the shield-building phase is marked by eruptions at Fang Ridge at ~1,000 ka. The termination of proto-Erebus eruptive activity is marked by the stratigraphically highest flow at Fang Ridge (758±20 ka). Younger lavas (~550–250 ka) on a modern-Erebus edifice are characterized by phonotephrites, tephriphonolites and trachytes. Plagioclase-phyric phonotephrite from coastal and flank flows yield ages between 531±38 and 368±18 ka. The initiation of anorthoclase tephriphonolite occurred in the southwest sector of the volcano at and around Turks Head (243±10 ka). A short pulse of effusive activity marked by crustal contamination occurred ~160 ka as indicated by at least two trachytic flows (157±6 and 166±10 ka). Most anorthoclase-phyric lavas, characteristic of Mt. Erebus, are less than 250 ka. All Mt. Erebus flows between about 250 and 90 ka are anorthoclase tephriphonolite in composition.Editorial responsibility: J. Donelly-Nolan     

The origin of Samoa: new evidence from Sr, Nd, and Pb isotopes

We report Sr, Nd and Pb isotope ratios and parent and daughter element concentrations in 34 volcanic rocks from Samoa. The highly undersaturated post-erosional volcanics, which have erupted in Recent to Historic time along a 250-km-long fissure, have isotopic compositions that define fields distinct from those of the tholeiitic to alkalic lavas of the older Samoan shield volcanoes. Most shield lavas have²⁰⁶Pb/²⁰⁴Pb of 18.9–19.4,⁸⁷Sr/⁸⁶Sr of 0.7045–0.7055 and⁸⁷Sr/⁸⁶Sr (to 0.7075). In general, isotopic compositions of the shield lavas are similar to those of the Marquesas and Society Islands. Post-erosional samples have lower²⁰⁶Pb/²⁰⁴Pb and¹⁴³Nd/¹⁴⁴Nd and higher⁸⁷Sr/⁸⁶Sr than most shield lavas. The most striking feature of the post-erosional data is a negative correlation between²⁰⁷Pb/²⁰⁴Pb and²⁰⁶Pb/²⁰⁴Pb. This suggests that post-erosional lavas are derived from mixtures of the shield source and a high-²⁰⁷Pb/²⁰⁴Pb,⁸⁷Sr/⁸⁶Sr, low-²⁰⁶Pb/²⁰⁴Pb and¹⁴³Nd/¹⁴⁴Nd post-erosional source which may contain recycled ancient sediment. This enriched mantle domain may also underlie the Ontong-Java and Manihiki Plateaus to the north and west. Although both the Samoan shield and post-erosional lavas show chemical characteristics often associated with mantle plumes, only the shield volcanism can plausibly be related to a plume. The post-erosional eruptions appear to be the result of flexure and rifting due to plate bending at the northern termination of the Tonga Trench.     

Geochemistry and Sr–Nd–Pb isotopic constraints on the petrogenesis of Cenozoic lavas from the Pali Aike and Morro Chico area (52°S), southern Patagonia,South America

Geochemical and isotopic analyses (Sr–Nd–Pb) of late Miocene to Quaternary plateau lavas from the Pali Aike and Morro Chico areas (52°S) were undertaken to constrain the melting processes and mantle sources that contributed to magma generation and the geodynamic evolution of southernmost Patagonia, South America. The Pali Aike and Morro Chico lavas are alkaline (Pali Aike, 45–49 wt.% SiO₂; 4.3–5.9 wt.% Na₂O+K₂O) and subalkaline (Morro Chico, 50.5–50.8 wt.% SiO₂; 4.0–4.4 wt.% Na₂O+K₂O), relatively primitive (Pali Aike, 9.5–13.7 wt.% MgO; Morro Chico, 7.6–8.8 wt.% MgO) mafic volcanic rocks that have typical intraplate ocean island basalt‐like signatures. Incompatible trace element ratios and isotopic ratios of the Pali Aike and Morro Chico lavas differ from those of the majority of Neogene southern Patagonian slab window lavas in showing more enriched characteristics and are similar to high‐μ (HIMU)‐like basalts. The rare earth element (REE) modeling to constrain mantle melting percentages suggests that these lavas were produced by low degrees of partial melting (1.0–2.0% for Pali Aike lavas and about 2.6–2.7% for Morro Chico lavas) of a garnet lherzolite mantle source. The major systematic variations of Sr–Nd–Pb isotopes in southern Patagonian lavas are related to geographic location. The Pali Aike and Morro Chico lavas from the southernmost part of Patagonia have lower ⁸⁷Sr/⁸⁶Sr and higher ¹⁴³Nd/¹⁴⁴Nd and ²⁰⁶Pb/²⁰⁴Pb ratios, relative to most of the southern Patagonian lavas erupted north of 49.5°S, pointing to a HIMU‐like signature. An isotopically depleted and HIMU‐like asthenospheric domain may have been the main source of magmas in the southernmost part of Patagonia (e.g. Pali Aike, Morro Chico, and Camusu Aike volcanic field), suggesting the presence of a major discontinuity in the isotopic composition of the asthenosphere in southern Patagonia. On the basis of geochemical and isotope data and the available geological and geotectonic reconstructions, a link between the HIMU asthenospheric mantle domain beneath southernmost Patagonia and the HIMU mega‐province of the southwestern Pacific Ocean is proposed.     

Petrogenesis of the late Cretaceous K‐rich volcanic rocks from the Central Pontide orogenic belt,North Turkey

Subduction‐related volcanic rocks are widespread in the Central Pontides of Turkey, and represented by the Hamsaros volcanic succession in the Sinop area to the north. The volcanic rocks display high‐K calc‐alkaline, shoshonitic and ultra‐K affinities. ⁴⁰Ar/³⁹Ar age data indicate that the rocks occurred during the Late Cretaceous (ca 82 Ma), and the volcanic suites were coeval. Primitive mantle‐normalized trace element patterns of all the lavas are characterized by strong enrichments in large ion lithophile elements (LILE) (Rb, Ba, K, and Sr), Th, U, Pb, and light rare earth elements (LREE; La, Ce) and prominent negative Nb, Ta, and Ti anomalies, all typical of subduction‐related lavas. There is a systematic increase in the enrichment of incompatible trace elements from the high‐K calc‐alkaline lavas through the shoshonitic to the ultra‐K lavas. In addition, the shoshonitic and ultra‐K lavas have significantly higher ⁸⁷Sr/⁸⁶Sr (0.70666–0.70834) and lower ¹⁴³Nd/¹⁴⁴Nd (0.51227–0.51236) initial ratios than coexisting high‐K calc‐alkaline lavas (⁸⁷Sr/⁸⁶Sr 0.70576–0.70613, ¹⁴³Nd/¹⁴⁴Nd 0.51245–0.51253). Geochemical and isotopic data show that the shoshonitic and ultra‐K rocks cannot be derived from the high‐K calc‐alkaline suite by any shallow level differentiation process, and point to a derivation from distinct mantle sources. The shoshonitic and ultra‐K rocks were derived from metasomatic veins related to melting of recycled subducted sediments, but the high‐K calc‐alkaline rocks from a lithospheric source metasomatized by fluids from subduction zone.     

Partial melting models for the petrogenesis of Reykjanes Peninsula basalts,Iceland Implications for the use of trace elements and strontium and neodymium isotope ratios to record inhomogeneities in the upper mantle

The mixing of magmas derived from two major compositional layers in a vertically stratified mantle has been favoured by Zindler et al. [1] in their interpretation of the REE and Sr and Nd isotope data for basalts from the Reykjanes Peninsula. However, a model involving the dynamic partial melting of a regionally homogeneous, veined mantle can also explain the major and trace element data and be reconciled with an alternative interpretation of the time relationships of the lavas to that presented by Jakobsson et al. [2]. Moreover, it is possible to explain the constant⁸⁷Sr/⁸⁶Sr but variable¹⁴³Nd/¹⁴⁴Nd ratios of the lavas by this model if the vein and wall rock components of the mantle source have equilibrated for Sr but not for Nd isotopes — a state that has been interpreted for some veined mantle nodules [13]. The model presented also involves more realistic degrees of partial melting than the alternative magma mixing models and satisfactorily explains the erupted volumes of the different magma types found in the area. Interpreting the basalt geochemistry in these terms suggests that Sr isotope ratios of the lavas monitor different scales of heterogeneity in the precursor mantle sources than Nd isotope ratios.     

Lead,uranium, strontium,potassium and rubidium in inclusion-bearing diamonds and mantle-derived xenoliths from Southern Africa

Measurements are reported of K, Rb and Sr levels and Sr isotopic compositions in silicate inclusions in diamonds, and of U, Th and Pb levels and Pb isotopic compositions in sulphide inclusions in diamonds. Samples are from the Premier Mine (Transvaal), the Finsch Mine (northern Cape Province) and the Kimberley mines (northern Cape Province). The isotopic composition of Pb in sulphide inclusions indicates that the diamonds containing these inclusions are xenocrysts in the host kimberlite. Model Pb ages for the sulphide inclusions in the diamonds from Finsch and Kimberley are in excess of 2 b.y., although the host kimberlites are Cretaceous. The sulphide inclusions from Premier, however, have a model age similar to the emplacement age of the Premier kimberlites (approximately 1.2 b.y.).In addition, K, Rb, Sr, U and Pb concentrations and Sr and Pb isotopic compositions in clinopyroxenes from 14 mantle-derived xenoliths were measured. Samples were eclogites from the Roberts Victor Mine (Orange Free State), peridotites from the Matsoku Pipe (Lesotho) and diopside megacrysts from the four mines in Kimberley. The samples from the Roberts Victor Mine define a large spread in Sr and Pb isotopic composition. The slope of a regression line through the Pb data in the 207/204 vs. 206/204 plot defines an age of roughly 2.5 b.y. The Matsoku samples have⁸⁷Sr/⁸⁶Sr ratios around 0.704. One group of samples (“fertile peridotites”) shows uniform, anomalously radiogenic Pb isotopic compositions, and bears evidence of a young event involving isotopic homogenisation. Lead isotopic heterogeneity, indicating an old age, has persisted in another group (“common peridotites”). The megacrysts from the four Kimberley mines have⁸⁷Sr/⁸⁶Sr ratios around 0.704 and uniform, anomalously radiogenic Pb isotopic compositions, indicating a young age. Their Pb isotopic uniformity contrasts with the spread shown by kimberlites in Kimberley, and shows that the megacrysts did not crystallise in equilibrium with their host kimberlites.The similarity between the Pb isotopic data obtained on clinopyroxenes from xenoliths and the data obtained on sulphide inclusions in diamonds from Finsch and Kimberley suggests that these diamonds might be cogenetic with old rock provinces in the subcontinental mantle.     

Pb, Nd, and Sr isotopic constraints on the origin of Miocene basaltic rocks from northeast Hokkaido, Japan: Implications for opening of the Kurile back-arc basin

Late Miocene (7–9 Ma) basaltic rocks from the Monbetsu‐Kamishihoro graben in northeast Hokkaido have chemical affinities to certain back‐arc basin basalts (referred to herein as Hokkaido BABB). Pb‐, Nd‐ and Sr‐isotopic compositions of the Hokkaido BABB and arc‐type volcanic rocks (11–13 Ma and 4–4.5 Ma) from the nearby region indicate mixing between the depleted mantle and an EM II‐like enriched component (e.g. subducted pelagic sediment) in the magma generation. At a given ⁸⁷Sr/⁸⁶Sr, Hokkaido BABB have slightly lower ¹⁴³Nd/¹⁴⁴Nd and slightly less radiogenic ²⁰⁶Pb/²⁰⁴Pb compared with associated arc‐type lavas, but both these suites are difficult to distinguish solely on the basis of isotopic compositions. These isotopic data indicate that while generation of the Hokkaido BABB involves smaller amounts of the EM II‐like enriched component than do associated arc lavas, Hokkaido BABB are isotopically distinct from basalts produced at normal back‐arc basin spreading centers. Instead, northeast Hokkaido BABB are more similar to basalts erupted during the initial rifting stage of back‐arc basins. The Monbetsu‐Kamishihoro graben may have developed in association with extension that formed the Kurile Basin, suggesting that opening of the basin continued until late Miocene (7–9 Ma).     

Potassium-rich volcanic rocks of the Muriah complex, Java, Indonesia: Products of multiple magma sources?

The extinct Pleistocene volcano Muriah, situated behind the main Pleistocene—Recent Sunda magmatic arc in north-central Java, has erupted at least two contrasted groups of lavas. One group forms a well-defined compositional series (Anhydrous Series) from leucite basanite to tephritic phonolite, with olivine and tschermakitic clinopyroxene the main phenocrysts. The other group, the “Hydrous Series”, includes compositionally variable tephrites and high-K andesites with common plagioclase, biotite and amphibole. Lavas of the Anhydrous Series are much richer in LIL trace elements than the most potassic lavas of neighbouring active volcanoes, but relative HFS element enrichment is less pronounced. REE patterns have almost constant slopes from La (250–600 times chondrites) to Yb (5–10 times chondrites), while those of lavas of active centres are less light-enriched, and show flattening in the heavy REE. Anhydrous Series initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043–0.7046) are lower than those of active centres (0.7047–0.7053). Hydrous Series lavas are intermediate in all these geochemical characteristics.The most mafic A-series leucite basanite, with Mg/(Mg + Fe²⁺) 0.69, 140 ppm Ni and 620 ppm Cr was probably derived from the primary magma for the series by fractionation of only 5 wt.% olivine. Its REE pattern suggests derivation from a garnet-bearing source. Experiments on this basanite, with up to 10% olivine and 20% orthopyroxene added, and in the presence of H₂O and H₂O/CO₂ mixtures, have shown that for all but very high magma water contents, the olivine and garnet liquidus fields are widely separated by fields of phlogopite and clinopyroxene. There is no liquidus field of orthopyroxene. Hence, if magma production involved an equilibrium melting process alone, the most probable sources are of garnet-bearing phlogopite clinopyroxenite type. Alternatively, this magma may represent the end-product of interaction between a low-K basanite magma from a garnet lherzolite source in the asthenosphere and a phlogopite-bearing lherzolite zone in the lower lithosphere. Its production was probably related to crustal doming and extension superimposed on the dominant subduction regime. Hydrous Series magmas may have resulted from mixing between Anhydrous Series magmas and high-K calc-alkaline basaltic to andesitic magmas more directly related to subduction processes.     

Assessment of a shallow magmatic system: the 1888–90 eruption,Vulcano Island,Italy

The magmatic system feeding the last eruption of the volcano La Fossa, Vulcano Island, Italy was studied. The petrogenetic mechanisms controlling the differentiation of erupted rocks were investigated through petrography, mineral chemistry, major, trace and rare earth element and Sr, Nd and Pb isotopic geochemistry. In addition, melt inclusion and fluid inclusion data were collected on both juvenile material and xenolithic partially melted metamorphic clasts to quantify the P-T conditions of the magma chamber feeding the eruption. A regular and continuous chemical zoning has been highlighted: rhyolites are the first erupted products, followed by trachytes and latites, whereas rhyolitic compositions were also found in the upper part of the sequence. The chemical and isotopic composition of the rhyolites indicates that they originated by fractional crystallization from latitic magmas plus the assimilation of crustal material; the trachytes represent hybrid magmas resulting from the mixing of latites and rhyolites, contaminated in the shallow magmatic system. The erupted products, primarily compositionally zoned from latites to rhyolites, are heterogeneous due to syn-eruptive mingling. The occurrence of magmacrust interaction processes, evidenced by isotopic variations (⁸⁷Sr/⁸⁶Sr=0.70474±3 to 0.70511±3; ¹⁴³Nd/¹⁴⁴Nd=0.512550±6 to 0.512614±8; ²⁰⁶Pb/²⁰⁴Pb=19.318–19.489; ²⁰⁷Pb/²⁰⁴Pb=15.642–15.782; ²⁰⁸Pb/²⁰⁴Pb=39.175–39.613), is confirmed by the presence of partially melted metamorphic xenoliths, with ⁸⁷Sr/⁸⁶Sr=0.71633±6 to 0.72505±2 and ¹⁴³Nd/¹⁴⁴Nd=0.51229±7, in rhyolites and trachytes. AFC calculations indicate a few percentage contribution of crustal material to the differentiating magmas. Thermometric measurements on melt inclusions indicate that the crystallization temperatures of the latites and trachytes were in the range of 1050–1100° C, whereas the temperature of the rhyolites appears to have been around 1000°C at the time of the eruption. Compositional data on melt inclusions reveal that the magmas involved in the eruption contained about 1–1.5 wt.% dissolved H₂O in pre-eruptive conditions. Secondary fluid inclusions found in metamorphic xenoliths give low equilibration pressure data (30–60 MPa), giving the location of the higher portions of the chamber at around 1500–2000 m of depth.     

Sr and Nd isotope geochemistry of coexisting alkaline magma series,Cantal, Massif Central,France

Sr and Nd isotope analyses are presented for Tertiary continental alkaline volcanics from Cantal, Massif Central, France. The volcanics belong to two main magma series, silica-saturated and silica-undersaturated (with rare nephelinites). Trace element and isotopic data indicate a common source for the basic parental magmas of both major series; the nephelinites in contrast must have been derived from a mantle source which is isotopically and chemically distinct from that which gave rise to the basalts and basanites.⁸⁷Sr/⁸⁶Sr initial ratios range from 0.7034 to 0.7056 in the main magma series (excluding rhyolites) and¹⁴³Nd/¹⁴⁴Nd ratios vary between 0.512927 and 0.512669; both are correlated with increasing SiO₂ in the lavas. The data can be explained by a model of crustal contamination linked with fractional crystallisation. This indicates that crustal magma chambers are the sites of differentiation since only rarely do evolved magmas not show a crustal isotopic signature and conversely basic magmas have primitive isotopic ratios unless they contain obvious crustal-derived xenocrysts. Potential contaminants include lower crustal granulites or partial melts of upper crustal units. Equal amounts of contamination are required for both magma series, refuting hypotheses of selective contamination of the silica-saturated series.The isotopic characteristics of the apparently primary nephelinite lavas demonstrates widespread heterogeneity in the mantle beneath Cantal. Some rhyolites, previously thought to be extremely contaminated or to be crustally derived, are shown to have undergone post-emplacement hydrothermal alteration.     

Geochemical and Sr–Nd–Pb isotopic investigation of Triassic granitoids and basement rocks in the northern Gyeongsang Basin, Korea: Implications for the young basement in the East Asian continental margin

Abstract We present chemical and Sr–Nd–Pb isotopic compositions of three Triassic (226–241 Ma) calc‐alkaline granitoids (the Yeongdeok granite, Yeonghae diorite and Cheongsong granodiorite) and basement rocks in the northern Gyeongsang basin, south‐eastern Korea. These plutons exhibit typical geochemical characteristics of I‐type granitoids generated in a continental magmatic arc. The Yeongdeok and Yeonghae plutons have similar initial Sr, Nd and Pb isotope ratios (⁸⁷Sr/⁸⁶Sr_initial = 0.7041 ~ 0.7050, ?_Nd(t) = 2.3 ~ 4.0, ²⁰⁶Pb/²⁰⁴Pb_feldspar = 18.22 ~ 18.34), but distinct rare earth element patterns, suggesting that the two plutons formed from partial melting of a similar source material at different depths. The Cheongsong pluton has slightly more enriched Sr–Nd–Pb isotopic compositions (⁸⁷Sr/⁸⁶Sr_initial = 0.7047 ~ 0.7065, ?_Nd(t) = 3.9 ~ 2.8, ²⁰⁶Pb/²⁰⁴Pb_feldspar = 18.24 ~ 18.37) than the other two plutons. The Nd model ages of the basement rocks (1.1 ~ 1.4 Ga) are slightly older than those of the plutons (0.6 ~ 1.0 Ga). The initial Sr and Nd isotopic ratios of the plutons can be modeled by the mixing between the mid‐oceanic ridge basalt‐like depleted mantle component and the crustal component represented by basement rocks, which is also supported by Pb isotope data. The Sr and Nd isotope data from granitoids and basement rocks suggest that the Gyeongsang basin, the Hida belt and the inner zone of south‐western Japan share relatively young basement histories (middle Proterozoic), compared with those (early Proterozoic to Archean) of the Gyeonggi and Yeongnam massifs and the Okcheon belt. The Nd isotope data of basement rocks suggest that the Hida belt might be better correlated with the basement of the Gyeongsang basin than the Gyeonggi massif, the Okcheon belt or the Yeongnam massif, although it may represent an older continental margin of East Asia than the Gyeongsang basin considering its slightly older Nd model ages.     

Petrogenesis of an 800 m lava sequence in eastern Uruguay: insights into magma chamber processes beneath the Paraná flood basalt province

Major and trace element along with representative Sr, Nd and Pb isotope data are presented for drill core samples which intersect an 800 m lava pile in eastern Uruguay. The lavas form part of the Paraná flood basalt province, are low-Ti in composition but distinct from the low-Ti Gramado magma type, and have been termed the Treinte Y Trés magma type. The lava pile overlies a large positive gravity anomaly inferred to reflect an east–west trending, mid-crustal mafic intrusive body with a calculated volume of 35,000 km³. Smooth up-section compositional variations in the basalts are interpreted to record magma evolution within this mid-crustal magma chamber. ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb increase throughout the sequence yet Mg remains relatively constant in the lower 200 m of the sequence, suggesting a role for magma chamber recharge. Above this the lavas show a regular, up-section decrease in Mg coupled with increasing ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb and this is interpreted to reflect crystal fractionation combined with crustal contamination. The data provide further evidence that contamination of flood basalt magmas in crustal magma chambers is a common phenomenon and calculations suggest that the amount of crustal addition may be as high as 60–70%. Nevertheless, the effects of this crustal contamination do not appear able to account for the discrepancy between key incompatible trace element ratios and isotope ratios of the lavas and those of any putative mantle plume. In fact, La/Ta decreases with decreasing Mg and increasing ⁸⁷Sr/⁸⁶Sr indicating that the effects of crustal contamination were actually to reduce La/Ta and implying that the parental magmas had very high La/Ta (90). These constraints are clearly inconsistent with an asthenospheric origin for the parental magmas and so, consistent with mass balance calculations, it is inferred that they were derived from the lithospheric mantle.     

Isotope geochemistry and origin of calc-alkaline lavas from a caledonian continental margin volcanic arc

Analyses for major and trace elements, including REE, and Sr, Nd and Pb isotopes are reported from a suite of Siluro-Devonian lavas from Fife, Scotland. The rocks form part of a major calc-alkaline igneous province developed on the Scottish continental margin above a WNW-dipping subduction zone. Within the small area (ca. 15 km²) considered, rock types range from primitive basalts and andesites (high Mg, Ni and Cr) to lavas more typical of modern calc-alkaline suites with less than 30 ppm Ni and Cr. There is a marked silica gap between these rocks (< 62%) and the rare rhyolites (> 74%), yet the latter can be generated by fractional crystallization from the more mafic lavas. In contrast, variation in incompatible element concentrations and ratios in the mafic lavas can not be generated by fractional crystallization processes. Increasing SiO₂ is accompanied by increasing Rb, K, Pb, U and Ba relative to Sr and high field strength elements, increasing LREE enrichment and increasing _Sr calculated at 410 Ma, and by decreasing HREE, Eu/Eu*, Sm/Nd and _Nd (410). _Nd and _Sr are roughly anticorrelated and have more radiogenic compositions than the mantle array, in common with data reported elsewhere from this part of the arc. The correlation extrapolates up to cross the mantle array within the composition field of the contemporary MORB source, and extrapolates down towards the probable compositional range of Lower Palaeozoic greywackes, which may form the uppermost 8 km of the crust, or may be supplied to the source by subduction. One sample, however, lies within the mantle array, and closely resembles lavas from northwestern parts of the arc, where a mantle source with mild time-integrated Rb/Sr and LREE enrichment has been inferred. The lavas have relatively high initial ²⁰⁷Pb/²⁰⁴Pb for their ²⁰⁶Pb/²⁰⁴Pb, a feature which has been interpreted elsewhere as the result of incorporation of a sediment component into arc magmas. The systematic changes with increasing SiO₂ in isotopic and chemical parameters can be explained by mixing of a greywacke-derived component with depleted mantle. The various possible mixing mechanisms are discussed, and it is considered most likely that mixing occurred in the mantle source through greywacke subduction. The bulk of the Rb, K, Ba and Pb in the lavas is probably recycled from the crust, whereas less than some 40% of the Sr and Nd is recycled. The calc-alkaline chemical trends are solely a function of mixing with the sediment component.     

Geochemistry of late Cenozoic lavas on Kunashir Island, Kurile Arc

Middle Miocene to Quaternary lavas on Kunashir Island in the southern zone of the Kurile Arc were examined for major, trace, and Sr–Nd–Pb isotope compositions. The lavas range from basalt through to rhyolite and the mafic lavas show typical oceanic island arc signatures without significant crustal or sub-continental lithosphere contamination. The lavas exhibit across-arc variation, with increasingly greater fluid-immobile incompatible element contents from the volcanic front to the rear-arc; this pattern, however, does not apply to some other incompatible elements such as B, Sb, and halogens. All Sr–Nd–Pb isotope compositions reflect a depleted source with Indian Ocean mantle domain characteristics. The Nd and Pb isotope ratios are radiogenic in the volcanic front, whereas Sr isotope ratios are less radiogenic. These Nd isotope ratios covary with incompatible element ratios such as Th/Nd and Nb/Zr, indicating involvement of a slab-derived sediment component by addition of melt or supercritical fluid capable of mobilizing these high field-strength elements and rare earth elements from the slab. Fluid mobile elements, such as Ba, are also elevated in all basalt suites, suggesting involvement of slab fluid derived from altered oceanic crust. The Kurile Arc lavas are thus affected both by slab sediment and altered basaltic crust components. This magma plumbing system has been continuously active from the Middle Miocene to the present.     

Geology and geochemistry of basaltic lava flows and dikes from the Trans-Koolau tunnel, Oahu, Hawaii

A 200-m section of Koolau basalt was sampled in the 1.6-km Trans-Koolau (T–K) tunnel. The section includes 126 aa and pahoehoe lava flows, five dikes and ten thin ash units. This volcanic section and the physical characteristics of the lava flows indicate derivation from the nearby northwest rift zone of the Koolau shield. The top of the section is inferred to be 500–600 m below the pre-erosional surface of the Koolau shield. Therefore, compared with previously studied Koolau lavas, this section provides a deeper, presumably older, sampling of the shield. Shield lavas from Koolau Volcano define a geochemical end-member for Hawaiian shields. Most of the tunnel lavas have the distinctive major and trace element abundance features (e.g. relatively high SiO₂ content and Zr/Nb abundance ratio) that characterize Koolau lavas. In addition, relative to the recent shield lavas erupted at Kilauea and Mauna Loa volcanoes, most Koolau lavas have lower abundances of Sc, Y and Yb at a given MgO content; this result is consistent with a more important role for residual garnet during the partial melting processes that created Koolau shield lavas. Koolau lavas with the strongest residual garnet signature have relatively high ⁸⁷Sr/⁸⁶Sr, ¹⁸⁷Os/¹⁸⁸Os, ¹⁸O/¹⁶O, and low ¹⁴³Nd/¹⁴⁴Nd. These isotopic characteristics have been previously interpreted to reflect a source component of recycled oceanic crust that was recrystallized to garnet pyroxenite. This component also has high La/Nb and relatively low ²⁰⁶Pb/²⁰⁴Pb, geochemical characteristics which are attributed to ancient pelagic sediment in the recycled crust. Although most Koolau lavas define a geochemical endmember for Hawaiian shield lavas, there is considerable intrashield geochemical variability that is inferred to reflect source characteristics. The oldest T–K tunnel lava flow is an example. It has the lowest ⁸⁷Sr/⁸⁶Sr, Zr/Nb and La/Nb, and the highest ¹⁴³Nd/¹⁴⁴Nd ratio found in Koolau lavas. In most respects it is similar to lavas from Kilauea Volcano. Therefore, the geochemical characteristics of the Koolau shield, which define an end member for Hawaiian shields, reflect an important role for recycled oceanic crust, but the proportion of this crust in the source varied during growth of the Koolau shield. Received: 1 June 1998 / Accepted: 30 August 1998     

Mantle plume heterogeneity versus shallow-level interactions: A case study,the São Nicolau Island,Cape Verde archipelago

We present new Sr–Nd–Pb isotopic data, as well as major- and trace-element concentrations, for 19 basaltic samples from São Nicolau Island, Cape Verde archipelago. Fine-scale study of the island argues in favor of mixing between four endmembers to explain isotopic variations of collected samples: 1) a radiogenic endmember (⁸⁷Sr/⁸⁶Sr ~ 0.7034; ¹⁴³Nd/¹⁴⁴Nd ~ 0.51285; ²⁰⁶Pb/²⁰⁴Pb ~ 20.0; ²⁰⁷Pb/²⁰⁴Pb ~ 15.65; ²⁰⁸Pb/²⁰⁴Pb ~ 39.8) representative of the Cape Verde plume deep source; 2) an unradiogenic endmember having isotopic compositions resembling those of Atlantic MORB dredged at the same latitude; 3) a low Sr–high Nd and Pb endmember identified as the Jurassic MORB basement of the archipelago; and 4) São Vicente-like Cape Verde carbonatites. Compositional and isotopic results show that most of the measured variations can be related to mixing of plume-derived melts with shallow-level reservoirs. Therefore the source heterogeneity of the Cape Verde plume is much smaller than the one sampled in basaltic samples. This observation illustrates how caution is required when interpreting global OIB data in terms of mantle topology without filtering from the contribution of shallow-level reservoirs.     

Enrichment of the continental lithosphere by OIB melts: Isotopic evidence from the volcanic province of northern Tanzania

Alkali basalts and nephelinites from the southern end of the East African Rift (EAR) in northern Tanzania have incompatible trace element compositions that are similar to those of ocean island basalts (OIB). They define a considerable range of Sr, Nd and Pb isotopic compositions (⁸⁷Sr/⁸⁶Sr= 0.7035−0.7058,ε_Nd = −5to+3, and²⁰⁶Pb/²⁰⁴Pb= 17.5−21.3), each of which partially overlaps the range found in OIB. However, they occupy a unique position in combined Nd, Sr and Pb isotopic compositional space. Nearly all of the lavas have radiogenic Pb, similar to HIMU with high time-integrated²³⁸U/²⁰⁴Pb coupled with unradiogenic Nd (+2 to −5) and radiogenic Sr (>0.704), similar to EMI. This combination has not been observed in OIB and provides evidence that these magmas predominantly acquired their Sr, Nd and Pb in the subcontinental lithospheric mantle rather than in the convecting asthenosphere. These data contrast with compositions for lavas from farther north in the EAR. The Pb isotopic compositions of basalts along the EAR are increasingly radiogenic from north to south, indicating a fundamental change to sources with higher time-integratedU/Pb, closer to the older cratons in the south. An ancient underplated OIB melt component, isolated for about 2 Ga as enriched lithospheric mantle and then remelted, could generate both the trace element and isotopic data measured in the Tanzanian samples. Whereas the radiogenic Pb in Tanzanian lavas requires a source with high time-integratedU/Pb, most continental basalts that are thought to have interacted with the continental lithospheric mantle have unradiogenic Pb, requiring a source with a history of lowU/Pb. Such lowU/Pb is readily accomplished with the addition of subduction-derived components, since the lower averageU/Pb of arc basalts (0.15) relative to OIB (0.36) probably reflects addition of Pb from subducted oceanic crust. If the subcontinental lithosphere is normally characterized by low time-integratedU/Pb it would appear that subduction magmatism is more important than OIB additions in supplying the Pb inventory of the lithospheric mantle. However,U/Pb ratios of xenoliths derived from the continental lithospheric mantle suggest that both processes may be important. This apparent discrepancy could be because xenoliths are not volumetrically representative of the subcontinental lithospheric mantle, or, more likely, that continental lithospheric mantle components in basalts are normally only identified as such when the isotopic ratios are dissimilar from MORB or OIB. Lithospheric enrichment from subaccreted OIB components appears to be more significant than generally recognized.     

Petrology and isotope-geochemistry of San Vincenzo rhyolites (Tuscany,Italy)

Two groups of rhyolites have been recognized at San Vincenzo (Tuscany, Italy). Group A rhyolites are characterized by plagioclase, quartz, biotite, sanidine and cordierite mineral assemblages. They show constant MgO and variable CaO and Na₂O contents. Initial⁸⁷Sr/⁸⁶Sr ratios in group A samples range between 0.71950 and 0.72535, whereas the Nd isotopic compositions are relatively constant (0.51215–0.51222). Group B rhyolites are characterized by orthopyroxene and clinopyroxene as additional minerals, and show textural, mineralogical and chemical evidence of interaction with more mafic magmas. The Sr and Nd isotopic ratios range between 0.71283–0.71542 and 0.51224–0.51227 respectively. Magmatic inclusions of variable size (1 mm to 10 cm) were found in groups B rhyolites. These inclusions consist mainly of diopsidic clinopyroxene and minor olivine and biotite. They are latitic in composition and represent blobs of hybrid intermediate magmas entrained in the rhyolitic melts. These magmatic inclusions have relatively high Sr contents (996–1529 ppm) and Sr and Nd isotope-ratios of 0.70807–0.70830 and 0.51245–0.51252 respectively.⁸⁷Sr/⁸⁷Sr data on minerals separated from both group A and B rhyolites and magmatic inclusions reveal strong isotopic disequilibria due to the presence of both restitic and newly crystallized phases in group A rhyolites and due to interaction of rhyolites with a mantle-de-rived magma in group B rhyolites. Isotopic data on whole rocks and minerals allow us to interpret the group A rhyolites as representative of different degrees of melting of an isotopically fairly homogeneous pelitic source; conversely, group B rhyolites underwent interactions with a mantle-derived magma. The crustal source as inferred from isotopic systematics would be characterized by⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd ratios close to 0.7194 and 0.51216 respectively. The sub-crustal magma would have Sr isotopic composition close to 0.7077 and a¹⁴³Nd/¹⁴⁴Nd ratio greater than or equal to 0.51252. These isotopic features are different from those reported for the parental magmas postulated for Vulsini and Alban Hills in the nearby Roman Magmatic Province, and are similar to those of the Vesuvius and Ischia magmas.     

The volcanic and magmatic evolution of Volcán Ollagüe, a high-K, late quaternary stratovolcano in the Andean Central Volcanic Zone

Volcán Ollagüe is a high-K, calc-alkaline composite volcano constructed upon extremely thick crust in the Andean Central Volcanic Zone. Volcanic activity commenced with the construction of an andesitic to dacitic composite cone composed of numerous lava flows and pyroclastic deposits of the Vinta Loma series and an overlying coalescing dome and coulée sequence of the Chasca Orkho series. Following cone construction, the upper western flank of Ollagüe collapsed toward the west leaving a collapse-amphitheater about 3.5 km in diameter and a debris avalanche deposit on the lower western flank of the volcano. The deposit is similar to the debris avalanche deposit produced during the May 18, 1980 eruption of Mount St. Helens, U.S.A., and was probably formed in a similar manner. It presently covers an area of 100 km² and extends 16 km from the summit. Subsequent to the collapse event, the upper western flank was reformed via eruption of several small andesitic lava flows from vents located near the western summit and growth of an andesitic dome within the collapse-amphitheater. Additional post-collapse activity included construction of a dacitic dome and coulée of the La Celosa series on the northwest flank. Field relations indicate that vents for the Vinta Loma and post-collapse series were located at or near the summit of the cone. The Vinta Loma series is characterized by an anhydrous, two-pyroxene assemblage. Vents for the La Celosa and Chasca Orkho series are located on the flanks and strike N55 W, radial to the volcano. The pattern of flank eruptions coincides with the distribution in the abundance of amphibole and biotite as the main mafic phenocryst phases in the rocks. A possible explanation for this coincidence is that an unexposed fracture or fault beneath the volcano served as a conduit for both magma ascent and groundwater circulation. In addition to the lava flows at Ollagüe, magmas are also present as blobs of vesiculated basaltic andesite and mafic andesite that occur as inclusions in nearly all of the lavas. All eruptive activity at Ollagüe predates the last glacial episode ( 11.000 a B.P.), because post-collapse lava flows are overlain by moraine and are incised by glacial valleys. Present activity is restricted to emission of a persistent, 100-m-high fumarolic steam plume from a vent located within the summit andesite dome.Sr and Nd isotope ratios for the basaltic andesite and mafic andesite inclusions and lavas suggest that they have assimilated large amounts of crust during crystal fractionation. In contrast, narrow ranges in ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr in the andesitic and dacitic lavas are enigmatic with respect to crustal contamination.