Petrology and Geochemistry of West Philippine Basin Basalts and Early Palau-Kyushu Arc Volcanic Clasts from ODP Leg 195, Site 1201D: Implications for the Early History of the Izu-Bonin-Mariana Arc

Site 1201D of Ocean Drilling Program Leg 195 recovered basalticand volcaniclastic units from the West Philippine Basin thatdocument the earliest history of the Izu–Bonin–Marianaconvergent margin. The stratigraphic section recovered at Site1201D includes 90 m of pillow basalts, representing the WestPhilippine Basin basement, overlain by 459 m of volcaniclasticturbidites that formed from detritus shed from the Eocene–Oligoceneproto-Izu–Bonin–Mariana island arc. Basement basaltsare normal mid-ocean ridge basalt (N-MORB), based on their abundancesof immobile trace elements, although fluid-mobile elements areenriched, similar to back-arc basin basalts (BABB). Sr, Nd,Pb and Hf isotopic compositions of the basement basalts aresimilar to those of basalts from other West Philippine Basinlocations, and show an overall Indian Ocean MORB signature,marked by high ²⁰⁸Pb/²⁰⁴Pb for a given ²⁰⁶Pb/²⁰⁴Pb and high¹⁷⁶Hf/¹⁷⁷Hf for a given ¹⁴³Nd/¹⁴⁴Nd. Trace element and isotopicdifferences between the basement and overlying arc-derived volcaniclasticsare best explained by the addition of subducted sediment orsediment melt, together with hydrous fluids from subducted oceaniccrust, into the mantle source of the arc lavas. In contrastto tectonic models suggesting that a mantle hotspot was a sourceof heat for the early Izu–Bonin–Mariana arc magmatism,the geochemical data do not support an enriched, ocean islandbasalt (OIB)-like source for either the basement basalts orthe arc volcanic section. KEY WORDS: back-arc basalts; Izu–Bonin–Marianas; Philippine Sea; subduction initiation; Ocean Drilling Program Leg 195     

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

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

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).     

Combined Trace Element and Pb-Nd-Sr-O Isotope Evidence for Recycled Oceanic Crust (Upper and Lower) in the Iceland Mantle Plume

We present the results of a comprehensive major element, traceelement and Sr–Nd–Pb–O isotopic study of post-glacialvolcanic rocks from the Neovolcanic zones on Iceland. The rocksstudied range in composition from picrites and tholeiites, whichdominate in the main rift systems, to transitional and alkalicbasalts confined to the off-rift and propagating rift systems.There are good correlations of rock types with geochemical enrichmentparameters, such as La/Sm and La/Yb ratios, and with long-termradiogenic tracers, such as Sr–Nd–Pb isotope ratios,indicating a long-lived enrichment/depletion history of thesource region. ⁸⁷Sr/⁸⁶Sr vs ¹⁴³Nd/¹⁴⁴Nd defines a negative array.Pb isotopes define well-correlated positive arrays on both ²⁰⁶Pb/²⁰⁴Pbvs ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb diagrams, indicating mixing ofat least two major components: an enriched component representedby the alkali basalts and a depleted component represented bythe picrites. In combined Sr–Nd–Pb isotopic spacethe individual rift systems define coherent mixing arrays withslightly different compositions. The enriched component hasradiogenic Pb (²⁰⁶Pb/²⁰⁴Pb > 19·3) and very similargeochemistry to HIMU-type ocean island basalts (OIB). We ascribethis endmember to recycling of hydrothermally altered upperbasaltic oceanic crust. The depleted component that is sampledby the picrites has unradiogenic Pb (²⁰⁶Pb/²⁰⁴Pb < 17·8),but geochemical signatures distinct from that of normal mid-oceanridge basalt (N-MORB). Highly depleted tholeiites and picriteshave positive anomalies in mantle-normalized trace element diagramsfor Ba, Sr, and Eu (and in some cases also for K, Ti and P),negative anomalies for Hf and Zr, and low ¹⁸O_olivine values(4·6–5·0) below the normal mantle range.All of these features are internally correlated, and we, therefore,interpret them to reflect source characteristics and attributethem to recycled lower gabbroic oceanic crust. Regional compositionaldifferences exist for the depleted component. In SW Icelandit has distinctly higher Nb/U (68) and more radiogenic ²⁰⁶Pb/²⁰⁴Pbratios (18·28–18·88) compared with the NErift (Nb/U 47; ²⁰⁶Pb/²⁰⁴Pb = 18·07–18·47).These geochemical differences suggest that different packagesof recycled oceanic lithosphere exist beneath each rift. A thirdand minor component with relatively high ⁸⁷Sr/⁸⁶Sr and ²⁰⁷Pb/²⁰⁴Pbis found in a single volcano in SE Iceland (Öræfajökullvolcano), indicating the involvement of recycled sediments inthe source locally. The three plume components form an integralpart of ancient recycled oceanic lithosphere. The slope in theuranogenic Pb diagram indicates a recycling age of about 1·5Ga with time-integrated Th/U ratios of 3·01. Surprisingly,there is little evidence for the involvement of North AtlanticN-MORB source mantle, as would be expected from the interactionof the Iceland plume and the surrounding asthenosphere in formof plume–ridge interaction. The preferential samplingof the enriched and depleted components in the off-rift andmain rift systems, respectively, can be explained by differencesin the geometry of the melting regions. In the off-rift areas,melting columns are truncated deeper and thus are shorter, whichleads to preferential melting of the enriched component, asthis starts melting deeper than the depleted component. In contrast,melting proceeds to shallower depths beneath the main rifts.The longer melting columns also produce significant amountsof melt from the more refractory (lower crustal/lithospheric)component. KEY WORDS: basalts; trace element and Sr, Nd, Pb, O isotope geochemistry; Iceland plume; isotope ratios; oceanic crustal recycling; partial melting; plume–ridge interaction     

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     

Lamproites from Gaussberg, Antarctica: Possible Transition Zone Melts of Archaean Subducted Sediments

Petrogenetic models for the origin of lamproites are evaluatedusing new major element, trace element, and Sr, Nd, and Pb isotopedata for Holocene lamproites from the Gaussberg volcano in theEast Antarctic Shield. Gaussberg lamproites exhibit very unusualPb isotope compositions (²⁰⁶Pb/²⁰⁴Pb = 17·44–17·55and ²⁰⁷Pb/²⁰⁴Pb = 15·56–15·63), which incommon Pb isotope space plot above mantle evolution lines andto the left of the meteorite isochron. Combined with very unradiogenicNd, such compositions are shown to be inconsistent with an originby melting of sub-continental lithospheric mantle. Instead,a model is proposed in which late Archaean continent-derivedsediment is subducted as K-hollandite and other ultra-high-pressurephases and sequestered in the Transition Zone (or lower mantle)where it is effectively isolated for 2–3 Gyr. The high²⁰⁷Pb/²⁰⁴Pb ratio is thus inherited from ancient continent-derivedsediment, and the relatively low ²⁰⁶Pb/²⁰⁴Pb ratio is the resultof a single stage of U/Pb fractionation by subduction-relatedU loss during slab dehydration. Sr and Nd isotope ratios, andtrace element characteristics (e.g. Nb/Ta ratios) are consistentwith sediment subduction and dehydration-related fractionation.Similar models that use variable time of isolation of subductedsediment can be derived for all lamproites. Our interpretationof lamproite sources has important implications for ocean islandbasalt petrogenesis as well as the preservation of geochemicallyanomalous reservoirs in the mantle. KEY WORDS: lamproites; Pb isotopes; mantle Transition Zone; subducted sediment; anomalous mantle reservoirs     

Carbonatite Magmatism and Plume Activity: Implications from the Nd, Pb and Sr Isotope Systematics of Oldoinyo Lengai

New Nd (0.51261–0.51268), Pb (²⁰⁶Pb/²⁰⁴Pb: 19.24–19.26),and Sr (0.70437–0.70446) isotopic compositions from tennatrocarbonatite lavas, collected in June 1993 from OldoinyoLengai, the only known active carbonatite volcano, are relativelyuniform, and are similar to data from the 1960 and 1988 flows.Three of the samples contain silicate spheroids, one of whichhas Nd and Sr isotopic ratios similar to host natrocarbonatite,consistent with an origin by liquid immiscibility or the mixingof melts with similar isotopic compositions. Pb isotope datafor two samples of trona are inconsistent with its involvementin the genesis of natrocarbonatite. New Pb isotope data fromsilicate volcanic and plutonic blocks (ijolite, nephelinite,phonolite, syenite) from Oldoinyo Lengai are highly variable(²⁰⁶Pb/²⁰⁴Pb, 17.75–19.34; ²⁰⁷Pb/²⁰⁴Pb, 15.41–15.67;²⁰⁸Pb/²⁰⁴Pb, 37.79–39.67), and define near-linear arraysin Pb-Pb diagrams. The isotopic data for the silicate rocksfrom Oldoinyo Lengai are best explained by invoking discretepartial melting events which generate undersaturated alkalinesilicate magmas with distinct isotopic ratios. Pb isotope ratiosfrom most ijolites and phonolites are predominantly lower andmore variable than from the natrocarbonatites, and are attributedto interaction between silicate melts involving HIMU and EMIsource components and an additional component, such as lower-crustalgranulites, DMM or PREMA (prevalent mantle). Variations in Nd,Pb and Sr isotope ratios from Oldoinyo Lengai, among the largestyet documented from a single volcano, are attributed to mantlesource heterogeneity involving mainly the mixing of HIMU andEMI mantle components. Based on the new isotopic data from OldoinyoLengai and data from other East African carbonatites, and mantlexenoliths, we propose a two-stage model in an attempt to explainthe isotope variations shown by carbonatites in this area. Themodel involves (I) the release of metasomatizing agents withHIMU-like signatures from upwelling mantle (‘plume’)source, which in turn metasomatize the sub-continental (old,isotopically enriched, EMI-like) lithosphere, and (2) variabledegrees and discrete partial melting of the resulting heterogeneous,metasomatized lithosphere. KEY WORDS: carbonatite; isotopes; Oldoinyo Lengai; mantle plumes ^*Telephone: (613) 788–2660, ext. 4419. Fax: (613) 788–4490. e-mail: kbell{at}ccs.carleton.ca     

The Origin of HIMU in the SW Pacific: Evidence from Intraplate Volcanism in Southern New Zealand and Subantarctic Islands

This paper presents field, geochemical and isotopic (Sr, Nd,Pb) results on basalts from the Antipodes, Campbell and ChathamIslands, New Zealand. New ⁴⁰Ar/³⁹Ar age determinations alongwith previous K–Ar dates reveal three major episodes ofvolcanic activity on Chatham Island (85–82, 41–35,5 Ma). Chatham and Antipodes samples comprise basanite, alkaliand transitional basalts that have HIMU-like isotopic (²⁰⁶Pb/²⁰⁴Pb>20·3–20·8, ⁸⁷Sr/⁸⁶Sr <0·7033,¹⁴³Nd/¹⁴⁴Nd >0·5128) and trace element affinities(Ce/Pb 28–36, Nb/U 34–66, Ba/Nb 4–7). Thegeochemistry of transitional to Q-normative samples from CampbellIsland is explained by interaction with continental crust. Thevolcanism is part of a long-lived (100 Myr), low-volume, diffusealkaline magmatic province that includes deposits on the Northand South Islands of New Zealand as well as portions of WestAntarctica and SE Australia. All of these continental areaswere juxtaposed on the eastern margin of Gondwanaland at >83Ma. A ubiquitous feature of mafic alkaline rocks from this regionis their depletion in K and Pb relative to other highly incompatibleelements when normalized to primitive mantle values. The inversionof trace element data indicates enriched mantle sources thatcontain variable proportions of hydrous minerals. We proposethat the mantle sources represent continental lithosphere thathost amphibole/phlogopite-rich veins formed by plume- and/orsubduction-related metasomatism between 500 and 100 Ma. Thestrong HIMU signature (²⁰⁶Pb/²⁰⁴Pb >20·5) is consideredto be an in-grown feature generated by partial dehydration andloss of hydrophile elements (Pb, Rb, K) relative to more magmaphileelements (Th, U, Sr) during short-term storage at the base ofthe lithosphere. KEY WORDS: continental alkaline basalts; lithospheric mantle, mantle metasomatism; New Zealand; OIB, HIMU; Sr, Nd and Pb isotopes; West Antarctica     

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

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

Lithospheric thickness beneath the southern Kenya Rift: implications from basalt geochemistry

Geochemical data are reported for samples from the flanks and floor of the southern Kenya Rift Valley in the Lake Magadi area, and from two central volcanoes located within the rift valley. Rift lavas include samples of Singaraini and Ol Tepesi basalts on the eastern flank, Kirikiti basalts from the western flank, and plateau trachytes from the rift valley floor. Central volcano samples are from Ol Esayeiti and Lenderut located on the eastern flank. The rift basalts are mildly ne-normative, moderately evolved (Mg#=0.39-0.62) alkali basalts and show an overall range in differentiation. Incompatible trace element abundances are moderately elevated (Nb=17-51; Zr=93-274; La=17-55 ppm) and show strongly coherent variations and constant inter-element ratios (e.g. Zr/Nb=4.2-5.5; Nb/Ta=17.5ǂ.4; (La/Sm)_n=7.3ǃ.1); isotope ratios are restricted in range (⁸⁷Sr/⁸⁶Sr=0.70393-0.70436; ¹⁴³Nd/¹⁴⁴Nd=0.51272-0.51280; ²⁰⁶Pb/²⁰⁴Pb=19.87-19.92; ²⁰⁷Pb/²⁰⁴Pb=15.68-15.70; ²⁰⁸Pb/²⁰⁴Pb=39.56-39.71). Central volcano lavas are more alkaline in character and include basanite (Ol Esayeiti; Mg# >60) and hawaiite to benmoreite (Lenderut; Mg#=0.48-0.38). Incompatible element ratio are similar to those of the rift basalts, although the chondrite normalised REE patterns are steeper (La/Sm)_n=17.4ǃ.2). ⁸⁷Sr/⁸⁶Sr (0.70358, 0.70391), ¹⁴³Nd/¹⁴⁴Nd (0.51280, 0.51267), ²⁰⁶Pb/²⁰⁴Pb (19.96,20.17), ²⁰⁷Pb/²⁰⁴Pb (15.66,15.76) and ²⁰⁸Pb/²⁰⁴Pb (39.80,40.00) ratios of Ol Esayeiti basanites are similar to the rift basalts, whereas the Lenderut lavas have unusually low¹⁴³Nd/¹⁴⁴Nd (0.512388-0.512453) ratios for their ⁸⁷Sr/⁸⁶Sr (0.70370-0.70481) ratios, and distinctly less radiogenic and variable Pb isotope compositions (²⁰⁶Pb/²⁰⁴Pb=17.93-19.01; ²⁰⁷Pb/²⁰⁴Pb=15.43-15.58; ²⁰⁸Pb/²⁰⁴Pb=37.91-39.14). An integrated model is developed in which the geochemical signature of the lavas is attributed to variable degrees of melting to depths within the garnet stability field, and in the presence of residual amphibole. The stability fields of these phases in P-T space indicates that the lavas must have formed within the sub-continental lithosphere rather than within the underlying ambient asthenosphere or a rising mantle plume. The subcontinental lithospheric mantle must therefore extend to a depth of at least 75 km beneath the Lake Magadi area, which contrasts with recent gravity models for the area, which infer that lithospheric mantle is absent beneath this section of the southern Kenya Rift.     

Isotope and Trace Element Geochemistry of Augustine Volcano, Alaska: Implications for Magmatic Evolution

Augustine Volcano, a Quaternary volcanic centre of the easternAleutian Arc, produces predominantly andesites and dacites oflow- to medium-K calc-alkaline composition. Mineralogical andmajor element characteristics of representative lavas suggestthat magmatic evolution has been influenced by both crystalfractionation and magma-mixing processes. However, incompatibletrace element variations (e.g. K/Rb) indicate that these evolvedlavas have been contaminated by the mafic arc crust of the underlyingTalkeetna accreted terrane. The limited range of isotope compositionsalso supports the assimilation of non-radiogenic mafic crust(e.g. ⁸⁷Sr/⁸⁶Sr = 0.7032–0.7034; ¹⁴³Nd/¹⁴⁴ Nd = 0.51301–0.5130).In addition, Pb-isotope compositions parallel the North Pacificmean oceanic trend (²⁰⁶Pb/²⁰⁴ Pb = 18.3–18.8; ²⁰⁷Pb/²⁰⁴Pb= 15.5–15.6; ²⁰⁸Pb/²⁰⁴Pb = 38.2–38.3) and do notrequire a subducted sediment component in the source. Relativelyhigh (Ba/La) N (0.79–18.10) and B/Be (14.5) ratios do,however, suggest a metasomatic fluid component derived fromthe dehydration of the subducting plate. The thickened continental crust (35 km) of the eastern AleutianArc prevents the ascent of basaltic melts, which fractionateand assimilate at various depths to produce andesitic magmas.These andesites evolve towards more silicic compositions byfractional crystallization. The absence of evidence for a largehigh-level crustal magma chamber implies that the magmatic systembeneath the volcano is young and at an immature stage of evolution. KEY WORDS: Augustine Volcano; Aleutians; assimilation; melasomatism; geochemistry ^*Corresponding author. Present address: Department of Geology and Geophysics, University of New Orleans, New Orleans, LA 70148, USA     

Open System Magmatic Evolution of the Taos Plateau Volcanic Field, Northern New Mexico: 3. Petrology and Geochemistry of Andesite and Dacite

Calc-alkaline olivine andesite and two-pyroxene dacite of theTaos Plateau volcanic field evolved in an open magmatic system.mg-numbers of spatially and temporally associated ServilletaBasalt (54–61) and ohvine andesite (49–59) are comparableand preclude fractional crystallization of ferromagnesian mineralsas the major differentiation process. If Servilleta olivinetholeiite is assumed to be the parental magma type, enrichmentsof highly incompatible trace elements (up to 17 ?) oVer concentrationsin the basalts require that andesitic and dacitic magmas containa substantial proportion of assimilated crust. Isotopic compositionsof andesite and dacite, which have slightly higher ⁸⁷Sr/⁸⁶Srratios than the basalts but lower ¹⁴³Nd/¹⁴⁴Nd, ²⁰⁶Pb/²⁰⁴Pb,²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios, are consistent with contaminationof parental basalt by old, low Rb/Sr, low U/Pb, and low Th/Pbcontinental crust. Concentrations of highly incompatible traceelements in andesite and dacite lavas are decoupled from majorelement compositions; the highest concentrat ions of these elementsoccur in andesitic, rather than dacitic compositions, and andesitelavas are more variable in trace element contents. Assimilationof heterogeneous crust concurrent with fractional crystallizationof varying mineral assemblages could cause this decoupled behavior.High mg-numbers in andesite and dacite, skeletal olivine phenocrysts,and reversely zoned pyroxene phenocrysts are manifestationsof mafic replenishment and magma mixing in the Taos Plateaumagmatic system. Taos Plateau volcanoes are monolithologic and are distributedin a semi-concentric zoned pattern that is a reflection of thecomplex subvolcanic magmatic system. A central focus of basaltshields developed above the main basaltic conduit system; thesemagmas contain 10–35% admixed andesitic and dacitic magma.Basalt shields are surrounded by a partial ring of olivine andesiteshield volcanoes, where replenishment of basaltic magma providedthe heat necessary for prolonged assimilation of crust, resultingin intermediate-composition lavas. Dacite shields are locatedaround the periphery of the more mafic volcanoes and reflecta decrease in mafic input on the fringes of the magmatic system.     

Systematic Variation of Sr-, Nd- and Pb-Isotopes with Time in Lavas of Mauritius, Reunion Hotspot

We report Sr-, Nd- and Pb-isotopic compositions for the lavasof Mauritius, the second youngest volcanic island in the Réunionhotspot. The lavas of the Older Series (7·8–5·5Ma) have identical isotopic compositions (⁸⁷Sr/⁸⁶Sr = 0·70411to 0·70422,¹⁴³Nd/¹⁴⁴Nd = 0·512865 to 0·512854,and ²⁰⁶Pb/²⁰⁴Pb = 19·016 to 19·041) to those ofRéunion, where the center of volcanic activity is currentlylocated. The lavas of the Intermediate Series (3·5–1·9Ma) and Younger Series (0·70–0·17 Ma) areshifted to lower Sr-isotopic compositions (0·70364–0·70394,with ¹⁴³Nd/¹⁴⁴Nd = 0·512813 to 0·512948 and ²⁰⁶Pb/²⁰⁴Pb= 18·794 to 18·984). The Intermediate Series lavashave similar trace-element characteristics (e.g. Zr–Nb,Ba–Y) to those of Rodrigues, in both cases requiring theinvolvement of an enriched mantle-like component in the mantlesource. During the volcanic history of Mauritius, the magmaslost the principal isotopic characteristics of the Réunionhotspot with time, and became gradually imprinted with the isotopicsignature of a shallower mantle source that produced the CentralIndian Ridge basalts. KEY WORDS: hotspot; isotopes; Mauritius; Réunion; trace element     

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     

Geochemical Evolution of Akagi Volcano, NE Japan: Implications for Interaction Between Island-arc Magma and Lower Crust, and Generation of Isotopically Various Magmas

Major and trace element, and Sr, Nd and Pb isotopic compositionswere determined for whole-rock samples from the ‘isotopicallyanomalous’ Akagi volcano in the volcanic front of theNE Japan arc. Sr and Nd isotopic compositions of phenocrystswere also analyzed together with their major and trace elementcompositions. Compared with the other volcanoes from the volcanicfront, the whole-rock isotope compositions of Akagi show highlyenriched characteristics; ⁸⁷Sr/⁸⁶Sr = 0·7060–0·7088,     

Petrogenesis of Pre-caldera Mafic Lavas, Jemez Mountains Volcanic Field (New Mexico, USA)

The Miocene–Quaternary Jemez Mountains volcanic field(JMVF), the site of the Valles caldera, lies at the intersectionof the Jemez lineament, a Proterozoic suture, and the CenozoicRio Grande rift. Parental magmas are of two types: K-depletedsilica-undersaturated, derived from the partial melting of lithosphericmantle with residual amphibole, and tholeiitic, derived fromeither asthenospheric or lithospheric mantle. Variability insilica-undersaturated basalts reflects contributions of meltsderived from lherzolitic and pyroxenitic mantle, representingheterogeneous lithosphere associated with the suture. The Kdepletion is inherited by fractionated, crustally contaminatedderivatives (hawaiites and mugearites), leading to distinctiveincompatible trace element signatures, with Th/(Nb,Ta) and La/(Nb,Ta)greater than, but K/(Nb,Ta) similar to, Bulk Silicate Earth.These compositions dominate the mafic and intermediate lavas,and the JMVF is therefore derived largely, and perhaps entirely,from melting of fertile continental Jemez lineament lithosphereduring rift-related extension. Significant variations in Pband Nd isotope ratios (²⁰⁶Pb/²⁰⁴Pb = 17·20–18·93;¹⁴³Nd/¹⁴⁴Nd = 0·51244–0·51272) result fromcrustal contamination, whereas ⁸⁷Sr/⁸⁶Sr is low and relativelyuniform (0·7040–0·7048). We compare theeffects of contamination by low-⁸⁷Sr/⁸⁶Sr crust with assimilationof high-⁸⁷Sr/⁸⁶Sr granitoid by partial melting, with Sr retainedin a feldspathic residue. Both models satisfactorily reproducethe isotopic features of the rocks, but the lack of a measurableEu anomaly in most JMVF mafic lavas is difficult to reconcilewith a major role for residual plagioclase during petrogenesis. KEY WORDS: Jemez Mountains volcanic field; Rio Grande rift; lithospheric mantle; crustal contamination; trace elements; radiogenic isotopes     

Trace Element and Isotope Geochemistry of the Volcanic Rocks of Bequia, Grenadine Islands, Lesser Antilles Arc: a Study of Subduction Enrichment and Intra-crustal Contamination

Pliocene volcanics on the island of Bequia comprise two interbeddedsuites of basalts and andesites. The isotopically homogeneoussuite (IHS) has a limited range of Sr—Nd—Pb isotopes(⁸⁷Sr/⁸⁶Sr 0.7040–0.7046, ¹⁴³ Nd/¹⁴⁴ Nd 0.5130 and ²⁰⁶Pb/²⁰⁴Pb 19.36–19.51), and mantle-like ¹⁸O values (5.5in clinopyroxene). The isotopically diverse suite (IDS) is characterizedby much wider ranges of radiogenic isotopes (⁸⁷ Sr/⁸⁶Sr 0.7048–0.7077,¹⁴³ Nd/¹⁴⁴ Nd 0.5128–0.5123 and ²⁰⁶ Pb/²⁰⁴ Pb 19.7–20.2),in which all of the Sr and Pb ratios are higher and Nd ratiosare lower than those of the IHS. The IDS is also characterizedby high ¹⁸ O values, up to 7.6 in clinopyroxene. The Sr andPb isotope ratios are too high, and the Nd isotope ratios aretoo low in the IDS for any of these lavas to be derived fromunmodified depleted mantle. Both suites are petrologically very similar and their majorelement compositions and phenocryst contents suggest that theywere formed largely by fractional crystallization of a hydroustholeiitic melt at pressures <3 kbar. The isotopic ratiosand enrichments in large ion lithophile elements (LILE), andto some extent light rare earth elements (LREE), as comparedwith mid-ocean ridge basalts (MORB), of the IHS lavas suggestthat they were derived from a depleted mantle source which hadbeen re-enriched by the addition of 1–4% of a subductioncomponent. This component probably comprised a mixture of dehydrationfluids, and perhaps minor siliceous melts, released from subductingsediments and mafic crust. The extreme isotopic ranges, largeenrichments in incompatible elements, more fractionated LREEpatterns and higher ¹⁸ O values of the IDS lavas are interpretedas resulting from 10–55% assimilation—fractionalcrystallization of sediments, derived from the Guyana Shield,which are present in the arc crust, by IHS type melts. KEY WORDS: trace elements; radiogenic isotopes; arc lavas; Lesser Antilles ^*Corresponding author.     

A Chemical and Multi-Isotope Study of the Western Cape Olivine Melilitite Province, South Africa: Implications for the Sources of Kimberlites and the Origin of the HIMU Signature in Africa

We present major and trace element and Sr–Nd–Pb–Hf–Osisotopic data for the 76–58 Ma Western Cape melilititeprovince, an age-progressive magmatic lineation in which primitiveolivine melilitite intrusives and alkali basalt lavas have beenemplaced on the southwestern margin of South Africa. The magmasrange from alkali basalts with strong HIMU isotopic and traceelement affinities on the continental shelf to melilitites withkimberlite-like incompatible element compositions and EM 1 isotopicaffinities on thick Proterozoic lithosphere (i.e. ⁸⁷Sr/⁸⁶Sr_i= 0·7029–0·7043,     

Petrology and Geochemistry of Eclogite Xenoliths from the Colorado Plateau: Implications for the Evolution of Subducted Oceanic Crust

Eclogite xenoliths from the Colorado Plateau, interpreted asfragments of the subducted Farallon plate, are used to constrainthe trace element and Sr–Nd–Pb isotopic compositionsof oceanic crust subducted into the upper mantle. The xenolithsconsist of almandine-rich garnet, Na-clinopyroxene, lawsoniteand zoisite with minor amounts of phengite, rutile, pyrite andzircon. They have essentially basaltic bulk-rock major elementcompositions; their Na₂O contents are significantly elevated,but K₂O contents are similar to those of unaltered mid-oceanridge basalt (MORB). These alkali element characteristics areexplained by spilitization or albitization processes on thesea floor and during subduction-zone metasomatism in the fore-arcregion. The whole-rock trace element abundances of the xenolithsare variable relative to sea-floor-altered MORB, except forthe restricted Zr/Hf ratios (36·9–37·6).Whole-rock mass balances for two Colorado Plateau eclogite xenolithsare examined for 22 trace elements, Rb, Cs, Sr, Ba, Y, rareearth elements, Pb, Th and U. Mass balance considerations andmineralogical observations indicate that the whole-rock chemistriesof the xenoliths were modified by near-surface processes afteremplacement and limited interaction with their host rock, aserpentinized ultramafic microbreccia. To avoid these secondaryeffects, the Sr, Nd and Pb isotopic compositions of mineralsseparated from the xenoliths were measured, yielding 0·70453–0·70590for ⁸⁷Sr/⁸⁶Sr, –3·1 to 0·5 for Nd and 18·928–19·063for ²⁰⁶Pb/²⁰⁴Pb. These isotopic compositions are distinctlymore radiogenic for Sr and Pb and less radiogenic for Nd thanthose of altered MORB. Our results suggest that the MORB-likeprotolith of the xenoliths was metasomatized by a fluid equilibratedwith sediment in the fore-arc region of a subduction zone andthat this metasomatic fluid produced continental crust-likeisotopic compositions of the xenoliths. KEY WORDS: Colorado Plateau; eclogite xenolith; geochemistry; subducted oceanic crust     

Constraints on the Source Components of Lavas Forming the Hawaiian North Arch and Honolulu Volcanics

Hawaiian volcanoes, dominantly shields of tholeiitic basalt,form as the Pacific Plate migrates over a hotspot in the mantle.As these shields migrate away from the hotspot, highly alkaliclavas, forming the rejuvenated stage of volcanism, may eruptafter an interval of erosion lasting for 0·25–2·5Myr. Alkalic lavas with geochemical characteristics similarto rejuvenated- stage lavas erupted on the sea floor north ofOahu along the Hawaiian Arch. The variable Tb/Yb, Sr/Ce, K/Ce,Rb/La, Ba/La, Ti/Eu and Zr/Sm ratios in lavas forming the NorthArch and the rejuvenated-stage Honolulu Volcanics were controlledduring partial melting by residual garnet, clinopyroxene, Fe–Tioxides and phlogopite. However, the distinctively high Ba/Thand Sr/Nd ratios of lava forming the North Arch and HonoluluVolcanics reflect source characteristics. These characteristicsare also associated with shield tholeiitic basalt; hence theyarise from the Hawaiian hotspot, which is interpreted to bea mantle plume. Inversion of the batch melting equation usingabundances of highly incompatible elements, such as Th and La,requires enriched sources with 10–55% clinopyroxene and5–25% garnet for North Arch lavas. The ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Ndratios in lavas forming the North Arch and Honolulu Volcanicsare consistent with mixing between the Hawaiian plume and adepleted component related to mid-ocean ridge basalts. Specifically,the enrichment of incompatible elements coupled with low ⁸⁷Sr/⁸⁶Srand high ¹⁴³Nd/¹⁴⁴Nd relative to bulk Earth ratios is best explainedby derivation from depleted lithosphere recently metasomatizedby incipient melt (<2% melting) from the Hawaiian plume.In this metasomatized source, the incompatible element abundances,as well as Sr and Nd isotopic ratios, are controlled by incipientmelts. In contrast, the large range of published ¹⁸⁷Os/¹⁸⁸Osdata (0·134–0·176) reflects heterogeneitycaused by various proportions of pyroxenite veins residing ina depleted peridotite matrix. KEY WORDS: Hawaiian plume; Honolulu Volcanics; North Arch; plume–lithosphere interaction; rejuvenated stage; trace element geochemistry; alkalic lavas