Contributions of Slab Fluid, Mantle Wedge and Crust to the Origin of Quaternary Lavas in the NE Japan Arc

Quaternary lavas from the NE Japan arc show geochemical evidenceof mixing between mantle-derived basalts and crustal melts atthe magmatic front, whereas significant crustal signals arenot detected in the rear-arc lavas. The along-arc chemical variationsin lavas from the magmatic front are attributable almost entirelyto geochemical variations in the crustal melts that were mixedwith a common mantle-derived basalt. The mantle-derived basaltshave slightly enriched Sr–Pb and depleted Nd isotopiccompositions relative to the rear-arc lavas, but the variationis less pronounced if crustal contributions are eliminated.Therefore, the source mantle compositions and slab-derived fluxesare relatively uniform, both across and along the arc. Despitethis, incompatible element concentrations are significantlyhigher in the rear-arc basalts. We examine an open-system, fluid-fluxedmelting model, assuming that depleted mid-ocean ridge basalt(MORB)-source mantle melted by the addition of fluids derivedfrom subducted oceanic crust (MORB) and sediment (SED) hybridsat mixing proportions of 7% and 3% SED in the frontal- and rear-arcsources, respectively. The results reproduce the chemical variationsfound across the NE Japan arc with the conditions: 0·2%fluid flux with degree of melting F = 3% at 2 GPa in the garnetperidotite field for the rear arc, and 0·7% fluid fluxwith F = 20% at 1 GPa in the spinel peridotite field beneaththe magmatic front. The chemical process operating in the mantlewedge requires: (1) various SED–MORB hybrid slab fluidsources; (2) variable amounts of fluid; (3) a common depletedmantle source; (4) different melting parameters to explain across-arcchemical variations. KEY WORDS: arc magma; crustal melt; depleted mantle; NE Japan; Quaternary; slab fluid     

Calc-alkaline, Shoshonitic, and Primitive Tholeiitic Lavas from Monogenetic Volcanoes near Crater Lake, Oregon

Quaternary monogenetic volcanism in the High Cascades of Oregonis manifested by cinder cones, lava fields, and small shields.Near Crater Lake caldera, monogenetic lava compositions include:low-K (as low as 0?09% K₂O) high-alumina olivine tholeiite (HAOT);medium-K. calc-alkaline basalt, basaltic andesite, and andesite;and shoshonitic basaltic andesite (2?1% K₂O, 1750 ppm Sr at54% SiO₂). Tholeiites have MORB-like trace element abundancesexcept for elevated Sr, Ba, and Th and low high field strengthelements (HFSE), and they represent near-primary liquids. Theyare similar to HAOTs from the Cascades and adjacent Basin andRange, and to many primitive basalts from intraoceanic arcs.Calc-alkaline lavas show a well-developed arc signature of highlarge-ion lithophile elements (LILE) and low HFSE. Their Zrand Hf concentrations are at least partly decoupled from thoseof Nb and Ta; HREE are low relative to HAOT. Incompatible elementabundances and ratios vary widely among basaltic andesites.Some calc-alkaline lavas vented near Mount Mazama contain abundantgabbroic microxcnoliths, and are basaltic andesitic magmas contaminatedwith olivine gabbro. A calc-alkaline basalt and a few basaltic andesites have MgOand compatible trace element contents that suggest only minorfractionation. There appears to be a compositional continuumbetween primitive tholeiitic and calc-alkaline lavas. Compositionalvariation within suites of comagmatic primitive lavas, boththoleiitic and calc-alkaline, mainly results from differentdegrees of partial melting. Sources of calc-alkaline primarymagmas were enriched in LILE and LREE by a subduction componentand contained residual garnet, whereas sources of HAOTs hadlower LILE and LREE concentrations and contained residual clinopyroxene.High and variable LILE and LREE contents of calc-alkaline lavasreflect variations in fluid-transported subduction componentadded to the mantle wedge, degree of partial melting, and possiblyalso interaction with rocks or partial melts in the lower crust. Andesites were derived from calc-alkaline basaltic andesitesby fractionation of plagioclase+augite+magnetite+apatite ? orthopyroxeneor olivine, commonly accompanied by assimilation. Many andesitesare mixtures of andesitic or dacitic magma and a basaltic orbasaltic andesitic component, or are contaminated with gabbroicmaterial. Mingled basalt, andesite, and dacite of Williams Craterformed by multi-component, multi-stage mixing of basaltic andesiticmagma, gabbro, and dacitic magma. The wide range of compositionsvented from monogenetic volcanoes near Crater Lake is a resultof the thick crust coupled with mild tectonic extension superimposedon a subduction-related magmatic arc.     

Chemical Diversity of the Ueno Basalts, Central Japan: Identification of Mantle and Crustal Contributions to Arc Basalts

The Ueno Basalts of central Japan comprise a monogenetic volcaniccone complex that was active between 2·76 and 1·34Ma. Basalts were erupted at more than 14 centers scattered overa region 40 km in diameter. Alkali basalt was erupted first,followed by sub-alkaline basalt. Quasi-concentric expansionof eruption centers coinciding with uplift and with decreasingalkalinity of the lavas suggests that Ueno magmatism originatedfrom a mantle diapir as it mushroomed at the base of the lithosphere.Depleted asthenospheric mantle (alkali basalt), enriched lithosphericmantle (sub-alkaline basalt), and crustal components are identifiedas chemical end-members in the petrogenesis of the Ueno Basalts.Incompatible trace element abundances indicate that the Uenoalkali basalts are typical within-plate basalts, whereas thesub-alkaline basalts show strong affinities with normal arclavas. Sr–Nd–Pb isotopic compositions indicate thatthe mantle source of the alkali basalts was more depleted thanthat of the sub-alkaline basalts. About 7% melting of asthenosphericmantle in the garnet-lherzolite stability field produced theprimitive alkali basalts and 12% melting of spinel lherzolitewithin the subcontinental lithosphere produced the primitivesub-alkaline basalts. Isotopic compositions and fluid mobile/immobileelement ratios broadly covary with SiO₂ contents in the sub-alkalinesuite, and increasing silica content is associated with strongerEMII (Enriched Mantle II) isotope affinities and fluid mobileelement abundances. A progressive AFC (assimilation–fractionalcrystallization) model assuming assimilation of a low-K silicicmelt reproduces the chemical variations observed in the sub-alkalinesuite. Melting of a flattening mantle diapir at the base ofthe lithosphere is the dominant cause of Ueno magmatism, accompaniedby the assimilation of older arc crust. KEY WORDS: arc basalt; crustal assimilation; mantle heterogeneity; Ueno Basalts     

Petrogenesis of Tertiary Continental Intra-plate Lavas from the Westerwald Region, Germany

Tertiary volcanic rocks from the Westerwald region range frombasanites and alkali basalts to trachytes, whereas lavas fromthe margin of the Vogelsberg volcanic field consist of morealkaline basanites and alkali basalts. Heavy rare earth elementfractionation indicates that the primitive Westerwald magmasprobably represent melts of garnet peridotite. The Vogelsbergmelts formed in the spinel–garnet peridotite transitionregion with residual amphibole for some magmas suggesting meltingof relatively cold mantle. Assimilation of lower-crustal rocksand fractional crystallization altered the composition of lavasfrom the Westerwald and Vogelsberg region significantly. Thecontaminating lower crust beneath the Rhenish Massif has a differentisotopic composition from the lower continental crust beneaththe Hessian Depression and Vogelsberg, implying a compositionalboundary between the two crustal domains. The mantle sourceof the lavas from the Rhenish Massif has higher ²⁰⁶Pb/²⁰⁴Pband ⁸⁷Sr/⁸⁶Sr than the mantle source beneath the Vogelsbergand Hessian Depression. The 30–20 Ma volcanism of theWesterwald apparently had the same mantle source as the QuaternaryEifel lavas, suggesting that the magmas probably formed in apulsing mantle plume with a maximum excess temperature of 100°Cbeneath the Rhenish Massif. The relatively shallow melting ofamphibole-bearing peridotite beneath the Vogelsberg and HessianDepression may indicate an origin from a metasomatized portionof the thermal boundary layer. KEY WORDS: continental rift volcanism; basanites; trachytes; assimilation; fractional crystallization; partial melting     

Origin of felsic volcanism in the Izu arc intra-arc rift

An intra-arc rift (IAR) is developed behind the volcanic front in the Izu arc, Japan. Bimodal volcanism, represented by basalt and rhyolite lavas and hydrothermal activity, is active in the IAR. The constituent minerals in the rhyolite lavas are mainly plagioclase and quartz, whereas mafic minerals are rare and are mainly orthopyroxene without any hydrous minerals such as amphibole and biotite. Both the phenocryst and groundmass minerals have felsic affinities with a narrow compositional range. The petrological and bulk chemical characteristics are similar to those of melts from some partial melting experiments that also yield dry rhyolite melts. The hydrous mineral-free narrow mineral compositions and low-Al₂O₃ affinities of the IAR rhyolites are produced from basaltic middle crust under anhydrous low-temperature melting conditions. The IAR basalt lavas display prominent across-arc variation, with depleted elemental compositions in the volcanic front side and enriched compositions in the rear-arc side. The across-arc variation reflects gradual change in the slab-derived components, as demonstrated by decreasing Ba/Zr and Th/Zr values to the rear-arc side. Rhyolite lavas exhibit different across-arc variations in either the fluid-mobile elements or the immobile elements, such as Nb/Zr, La/Yb, and chondrite-normalized rare earth element patterns, reflecting that the felsic magmas had different source. The preexisting arc crust formed during an earlier stage of arc evolution, most probably during the Oligocene prior to spreading of the Shikoku back-arc basin. The lack of systematic across-arc variation in the IAR rhyolites and their dry/shallow crustal melting origin combines to suggest re-melting of preexisting Oligocene middle crust by heat from the young basaltic magmatism.     

Geochemistry of basaltic lavas from the southern Lau Basin: input of compositionally variable subduction components

We present new major element, trace element, and Sr–Nd–Pb isotope data for 18 basaltic lavas and six glasses collected in situ from the Eastern Lau Spreading Centre (ELSC) and the Valu Fa Ridge (VFR). All lava samples are aphanitic and contain rare plagioclase and clinopyroxene microlites and microphenocrysts. The rocks are sub-alkaline and range from basalt and basaltic andesite to more differentiated andesite. In terms of trace element compositions, the samples are transitional between typical normal mid-ocean ridge basalt (MORB) and island arc basalt. Samples from the VFR have higher large ion lithophile element/high field strength element ratios (e.g. Ba/Nb) than the ELSC samples. VFR and ELSC Sr–Nd isotopic compositions plot between Indian MORB and Tonga arc lavas, but VFR samples have higher ⁸⁷Sr/⁸⁶Sr for a given ¹⁴³Nd/¹⁴⁴Nd ratio than ELSC analogues. The Pb isotopic composition of ELSC lavas is more Indian MORB-like, whereas that of VFR lavas is more Pacific MORB-like. Our new data, combined with literature data for the Central Lau Spreading Centre, indicate that the mantle beneath the ELSC and VFR spreading centres was originally of Pacific type in composition, but was displaced by Indian-type mantle as rifting propagated to the south. The mantle beneath the spreading centres also was variably affected by subduction-induced metasomatism, mainly by fluids released from the altered, subducting oceanic crust; the influence of these components is best seen in VFR lavas. To a first approximation, the effects of underflow on the composition and degree of partial melting of the mantle source of Lau spreading centre lavas inversely correlate with distance of the spreading centres from the Tonga arc. Superimposed on this general process, however, are the effects of the local geographic contrasts in the composition of subduction components. The latter have been transferred mainly by dehydration-generated fluids into the mantle beneath the Tonga supra-subduction zone.     

Subduction Influence on Oxygen Fugacity and Trace and Volatile Elements in Basalts Across the Cascade Volcanic Arc

Fluids or melts derived from a subducting plate are often citedas a mechanism for the oxidation of arc magmas. What remainsunclear is the link between the fluid, oxygen fugacity, andother major and trace components, as well as the spatial distributionof the impact of those fluids. To test the potential effectsof addition of a subduction-derived fluid or melt to the sub-arcmantle, olivine-hosted melt inclusions from primitive basalticlavas sampled from across the central Oregon Cascades (43°–45°N)have been analyzed for major, trace and volatile elements andfO₂. Oxygen fugacity was determined in melt inclusions fromsulfur speciation determined by electron microprobe and fromolivine–chromite oxygen geobarometry. The overall rangein fO₂ based on sulfur speciation measurements is from <–0·25log units to + 1·9 log units (FMQ, where FMQ is fayalite–magnetite–quartzbuffer). Oxygen fugacity is positively correlated with fluid-mobiletrace element and light rare earth element contents in basaltsgenerated by relatively low-degree partial melting. Establishinga further correlation between fO₂ and fluid-mobile trace elementabundances with position along the arc requires the basaltsto be subdivided into shoshonitic, calc-alkaline, low-K tholeiiteand enriched intraplate basalt groups. Melt inclusions fromenriched intraplate and shoshonitic lavas show increasing fO₂and trace element abundances closer to the trench, whereas calc-alkalinemelt inclusions exhibit no significant across-arc variations.Low-K tholeiitic melt inclusions record an increase in incompatibletrace elements closer to the trench; however, there is no correlatedincrease in fO₂. The correlation observed in enriched intraplateand shoshonitic melt inclusions is interpreted to reflect aprogressively greater proportion of a fluid-rich, oxidized subductioncomponent in magmas generated nearer the subduction zone. Significantly,calc-alkaline melt inclusions with high ratios of large ionlithophile elements to high field strength elements, characteristicof ‘typical’ arc magmas, have oxidation states indistinguishablefrom low-K tholeiite and enriched intraplate basalt melt inclusions.The lack of across-arc geochemical variation in calc-alkalinemelt inclusions may suggest that these basalts are not necessarilythe most appropriate magmas for examining recent addition ofa subduction component to the sub-arc mantle. Flux and batchmelt model results produce a wide range of predicted amountsof melting and subduction component added to the mantle source;however, general trends characterized by increased melting andproportion of the subduction component from enriched intraplate,to low-K tholeiite, to calc-alkaline are robust. The model resultsdo not require enriched intraplate, low-K tholeiite and calc-alkalinemagmas to be produced from the same more fertile mantle source.However, enriched intraplate magmas, in contrast to calc-alkalineand low-K tholeiite magmas, cannot be generated from a depletedmantle source. Flux or batch melting of either the more fertileor depleted mantle sources used to generate the low-K tholeiite,calc-alkaline, and enriched intraplate magmas cannot reproduceshoshonitic compositions, which require a significantly depletedmantle source strongly metasomatized by a subduction component.The potential mantle source for shoshonitic basalts has a predictedfO₂ (after oxidation) from + 0·3 to + 2·4 logunits (FMQ) whereas the mantle source for low-K tholeiite, calc-alkaline,and enriched intraplate magmas may range from –1·1to + 0·7 log units (FMQ). KEY WORDS: basalt; Cascades; melt inclusions; oxidation state; volatiles     

Volatiles in Basaltic Glasses from Loihi Seamount, Hawaii: Evidence for a Relatively Dry Plume Component

New H₂O, CO₂ and S concentration data for basaltic glasses fromLoihi seamount, Hawaii, allow us to model degassing, assimilation,and the distribution of major volatiles within and around theHawaiian plume. Degassing and assimilation have affected CO₂and Cl but not H₂O concentrations in most Loihi glasses. Waterconcentrations relative to similarly incompatible elements inHawaiian submarine magmas are depleted (Loihi), equivalent (Kilauea,North Arch, Kauai–Oahu), or enriched (South Arch). H₂O/Ceratios are uncorrelated with major element composition or extentor depth of melting, but are related to position relative tothe Hawaiian plume and mantle source region composition, consistentwith a zoned plume model. In front of the plume core, overlyingmantle is metasomatized by hydrous partial melts derived fromthe Hawaiian plume. Downstream from the plume core, lavas tapa depleted source region with H₂O/Ce similar to enriched Pacificmid-ocean ridge basalt. Within the plume core, mantle components,thought to represent subducted oceanic lithosphere, have waterenrichments equivalent to (KEA) or less than (KOO) that of Ce.Lower H₂O/Ce in the KOO component may reflect efficient dehydrationof the subducting oceanic crust and sediments during recyclinginto the deep mantle. KEY WORDS: basalt; Hawaii; mantle; plumes; volatiles     

Rare earth element evidence concerning the origin of voluminous mid-Tertiary rhyolitic ignimbrites and related volcanic rocks,Sierra Madre Occidental,Chihuahua, Mexico

The mid-Tertiary volcanic sequence of the central Sierra Madre Occidental in Chihuahua, Mexico, is about one kilometer thick and is composed predominantly of rhyolitic ignimbrites. Basaltic andesite to dacitic lavas are interbedded with the rhyolites, but they are of minor volumetric importance. Rare earth element (REE) data are used to constrain a crustal anatexis model for the origin of the voluminous ignimbrites and to test a fractional crystallization model. The REE patterns indicate that if the rhyolites were formed by direct crustal anatexis, the residue from partial melting could contain no more than a few percent garnet or about 20% hornblende. This eliminates residues with the mineralogy of amphibolite, eclogite, or garnet granulite, but melting of a garnet-free granulite source is permitted. The crustal anatexis model is difficult to evaluate critically because of a lack of knowledge concerning the mid-Tertiary geothermal gradient and the composition of the crust beneath the Sierra Madre Occidental.In contrast, the fractional crystallization model can be tested rigorously. Rayleigh fractionation calculations are used to closely model REE patterns in the basaltic andesite to rhyolite series. The minerals involved are those occurring as phenocryst phases, and the mineral proportions were generated by leastsquares major element calculations. The results of the calculations are consistent with the hypothesis that the voluminous rhyolites originated by plagioclase-dominated crystal fractionation.     

Lower Crustal Magma Genesis and Preservation: a Stochastic Framework for the Evaluation of Basalt-Crust Interaction

We present a quantitative assessment of the thermal and dynamicresponse of an amphibolitic lower crust to the intrusion ofbasaltic dike swarms in an arc setting. We consider the effectof variable intrusion geometry, depth of intrusion, and basaltflux on the production, persistence, and interaction of basalticand crustal melt in a stochastic computational framework. Distinctmelting and mixing environments are predicted as a result ofthe crustal thickness and age of the arc system. Shallow crustal(30 km) environments and arc settings with low fluxes of mantle-derivedbasalt are likely repositories of isolated pods of mantle andcrustal melts in the lower crust, both converging on daciticto rhyodacitic composition. These may be preferentially rejuvenatedin subsequent intrusive episodes. Mature arc systems with thickercrust (50 km) produce higher crustal and residual basaltic meltfractions, reaching 0·4 for geologically reasonable basaltfluxes. The basaltic to basaltic andesite composition of bothcrustal and mantle melts will facilitate mixing as the networkof dikes collapses, and Reynolds numbers reach 10^–4–1·0in the interiors of dikes that have been breached by ascendingcrustal melts. This may provide one mechanism for melting, assimilation,storage and homogenization (MASH)-like processes. Residual mineralassemblages of crust thickened by repeated intrusion are predictedto be garnet pyroxenitic, which are denser than mantle peridotiteand also generate convective instabilities where some of thecrustal material is lost to the mantle. This reconciles thethinner than predicted crust in regions that have undergonea large flux of mantle basalt for a prolonged period of time,and helps explain the enrichment of incompatible elements suchas K₂O, typical of mature arc settings, without the associatedmass balance problem. KEY WORDS: crustal anatexis; delamination; lower crust; magma mixing; thermal model     

Remelting of an Andesitic Crust as a Possible Origin for Rhyolitic Magma in Oceanic Arcs: an Example from the Izu-Bonin Arc

The Izu–Bonin volcanic arc is an excellent example ofan intra-oceanic convergent margin. A total of 1011 chemicalanalyses of 17 Quaternary volcanoes of the arc are reviewedto estimate relative proportions of magmas erupted. Basalt andbasic andesite (SiO₂ < 57 wt %) are the predominant eruptiveproducts of the Izu–Bonin arc, and rhyolite (SiO₂ >70 wt %) forms another peak in volume. Such rhyolites possesscompositions identical to those of partial melts produced bydehydration-melting of calc-alkaline andesites at low pressure(<7 kbar). Meanwhile, the major element variation of theShirahama Group Mio-Pliocene volcanic arc suite, Izu Peninsula,completely overlaps that of the Quaternary Izu–Bonin arcvolcanoes, and groundmasses of Shirahama Group calc-alkalineandesites have compositions similar to those of Izu–Boninrhyolites. Moreover, phenocryst assemblages of calc-alkalineandesites of the Shirahama Group resemble restite phase assemblagesof dehydration-melting of calc-alkaline andesite. These linesof evidence suggest that the rhyolite magmas may have been producedby dehydration-melting of calc-alkaline andesite in the upperto middle crust. If so, then the presence of large amounts ofcalc-alkaline andesite (3–5 times more abundant than therhyolites) within the oceanic arc crust would be expected, whichis consistent with a recently proposed structural model acrossthe Izu–Bonin arc. The calc-alkaline andesite magmas maybe water saturated, and would crystallize extensively and solidifywithin the crust. The model proposed here suggests that rhyoliteeruptions could be triggered by an influx of hot basalt magmafrom depth, reheating and partially melting the calc-alkalineandesite component of the crust. KEY WORDS: bimodal magmatism; calc-alkaline andesite; oceanic arcs; rhyolite     

Carbonate Assimilation at Merapi Volcano, Java, Indonesia: Insights from Crystal Isotope Stratigraphy

Recent basaltic andesite lavas from Merapi volcano contain abundant,complexly zoned, plagioclase phenocrysts, analysed here fortheir petrographic textures, major element composition and Srisotope composition. Anorthite (An) content in individual crystalscan vary by as much as 55 mol% (An_40–95) across internalresorption surfaces with a negative correlation between highAn mol% (>70), MgO wt% and FeO wt%. In situ Sr isotope analysesof zoned plagioclase phenocrysts show that the ⁸⁷Sr/⁸⁶Sr ratiosof individual zones range from 0·70568 to 0·70627.The upper end of this range is notably more radiogenic thanthe host basaltic andesite whole-rocks (< 0·70574).Crystal zones with the highest An content have the highest ⁸⁷Sr/⁸⁶Srvalues, requiring a source or melt with elevated radiogenicSr, rich in Ca and with lower Mg and Fe. Recent Merapi eruptiverocks contain abundant xenoliths, including metamorphosed volcanoclasticsediment and carbonate country rock (calc-silicate skarns) analysedhere for petrographic textures, mineralogy, major element compositionand Sr isotope composition. The xenoliths contain extremelycalcic plagioclase (up to An₁₀₀) and have whole-rock ⁸⁷Sr/⁸⁶Srratios of 0·70584 to 0·70786. The presence ofthese xenoliths and their mineralogy and geochemistry, coupledwith the ⁸⁷Sr/⁸⁶Sr ratios observed in different zones of individualphenocrysts, indicate that magma–crust interaction atMerapi is potentially more significant than previously thought,as numerous crystal cores in the phenocrysts appear to be inheritedfrom a metamorphosed sedimentary crustal source. This has potentiallysignificant consequences for geochemical mass-balance calculations,volatile saturation and flux and eruptive behaviour at Merapiand similar island arc volcanic systems elsewhere. KEY WORDS: assimilation; isotopes; Merapi; xenolith; calc-silicate     

Silica-rich Melts in Quartz Xenoliths from Vulcano Island and their Bearing on Processes of Crustal Anatexis and Crust-Magma Interaction beneath the Aeolian Arc, Southern Italy

Quartz-rich xenoliths in lavas and pyroclastic rocks from VulcanoIsland, part of the Aeolian arc, Italy, contain silicic meltinclusions with high SiO₂ (73–80 wt %) and K₂O (3–6wt %) contents. Two types of inclusions can be distinguishedbased on their time of entrapment and incompatible trace element(ITE) concentrations. One type (late, ITE-enriched inclusions)has trace element characteristics that resemble those of themetamorphic rocks of the Calabro-Peloritano basement of theadjacent mainland. Other inclusions (early, ITE-depleted) havevariable Ba, Rb, Sr and Cs, and low Nb, Zr and rare earth element(REE) contents. Their REE patterns are unfractionated, witha marked positive Eu anomaly. Geochemical modelling suggeststhat the ITE-depleted inclusions cannot be derived from equilibriummelting of Calabro-Peloritano metamorphic rocks. ITE-enrichedinclusions can be modelled by large degrees (>80%) of meltingof basement gneisses and schists, leaving a quartz-rich residuerepresented by the quartz-rich xenoliths. Glass inclusions inquartz-rich xenoliths represent potential contaminants of Aeolianarc magmas. Interaction between calc-alkaline magmas and crustalanatectic melts with a composition similar to the analysed inclusionsmay generate significant enrichment in potassium in the magmas.However, ITE contents of the melt inclusions are comparablewith or lower than those of Vulcano calc-alkaline and potassicrocks. This precludes the possibility that potassic magmas inthe Aeolian arc may originate from calc-alkaline parents throughdifferent degrees of incorporation of crustal melts. KEY WORDS: melt inclusions; crustal anatexis; magma assimilation; xenoliths; Vulcano Island     

Mafic magmas from Mount Baker in the northern Cascade arc,Washington: probes into mantle and crustal processes

Five mafic lava flows located on the southern flank of Mount Baker are among the most primitive in the volcanic field. A comprehensive dataset of whole rock and mineral chemistry reveals the diversity of these mafic lavas that come from distinct sources and have been variably affected by ascent through the crust. Disequilibrium textures present in all of the lavas indicate that crustal processes have affected the magmas. Despite this evidence, mantle source characteristics have been retained and three primitive endmember lava types are represented. These include (1) modified low-K tholeiitic basalt (LKOT-like), (2) typical calc-alkaline (CA) lavas, and (3) high-Mg basaltic andesite and andesite (HMBA and HMA). The Type 1 endmember, the basalt of Park Butte (49.3–50.3 wt% SiO₂, Mg# 64–65), has major element chemistry similar to LKOT found elsewhere in the Cascades. Park Butte also has the lowest overall abundances of trace elements (with the exception of the HREE), indicating it is either derived from the most depleted mantle source or has undergone the largest degree of partial melting. The Type 2 endmember is represented by the basalts of Lake Shannon (50.7–52.6 wt% SiO₂, Mg# 58–62) and Sulphur Creek (51.2–54.6 wt% SiO₂, Mg# 56–57). These two lavas are comparable to calc-alkaline rocks found in arcs worldwide and have similar trace element patterns; however, they differ from each other in abundances of REE, indicating variation in degree of partial melting or fractionation. The Type 3 endmember is represented by the HMBA of Tarn Plateau (51.8–54.0 wt% SiO₂, Mg# 68–70) and the HMA of Glacier Creek (58.3–58.7 wt% SiO₂, Mg# 63–64). The strongly depleted HREE nature of these Type 3 units and their decreasing Mg# with increasing SiO₂ suggests fractionation from a high-Mg basaltic parent derived from a source with residual garnet. Another basaltic andesite unit, Cathedral Crag (52.2–52.6 wt% SiO₂, Mg# 55–58), is an Mg-poor differentiate of the Type 3 endmember. The calc-alkaline lavas are least enriched in a subduction component (lowest H₂O, Sr/P_N, and Ba/Nb), the LKOT-like lavas are intermediate (moderate Sr/P_N and Ba/Nb), and the HMBA are most enriched (highest H₂O, Sr/P_N and Ba/Nb). The generation of the LKOT-like and calc-alkaline lavas can be successfully modeled by partial melting of a spinel lherzolite with variability in composition of slab flux and/or mantle source depletion. The HMBA lavas can be successfully modeled by partial melting of a garnet lherzolite with slab flux compositionally similar to the other lava types, or less likely by partial melting of a spinel lherzolite with a distinctly different, HREE-depleted slab flux.     

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

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

Andesites from northeastern Kanaga Island,Aleutians

Kanaga island is located in the central Aleutian island arc. Northeastern Kanaga is a currently active late Tertiary to Recent calc-alkaline volcanic complex. Basaltic andesite to andesite lavas record three episodes (series) of volcanic activity. Series I and Series II lavas are all andesite while Series III lavas are basaltic andesite to andesite. Four Series II andesites contain abundant quenched magmatic inclusions ranging in composition from high-MgO low-alumina basalt to low-MgO highalumina basalt. The spectrum of lava compositions is due primarily to fractional crystallization of a parental low-MgO high-alumina basalt but with variable degrees of crustal contamination and magma mixing. The earliest Series I lavas represent mixing between high-alumina basalt and silicic andesite with maximum SiO₂ contents of 65–67 wt %. Later Series I and all Series II lavas are due to mixing of andesite magmas of similar composition. The maximum SiO₂ content of the pre-mixed andesites magmas is estimated at 60–63 wt %. The youngest lavas (Series III) are all non-mixed and have maximum estimated SiO₂ contents of 59 wt %. The earliest Series I lavas contain a significant crustal component while all later lavas do not. It is concluded that the maximum SiO₂ contents of silicic magmas, the contribution of crustal material to silicic magma generation, and the role of magma mixing all decrease with time. Furthermore, silicic magmas generated by fractional crystallization at this volcanic center have a maximum SiO₂ content of 63 wt %. All of these features have also been documented at the central Aleutian Cold Bay Volcanic Center (Brophy 1987). Based on data from these two centers a model of Aleutian calc-alkaline magma chamber development is proposed. The main features are: (1) a single low pressure magma chamber is continuously supplied by primitive low-alumina basalt; (2) non-primary high-alumina basalt is formed along the chamber margins by selective gravitational settling of olivine and clinopyroxene and retention of plagioclase; (3) sidewall crystallization accompanied by crustal melting produces buoyant silicic (>63 wt % SiO₂) liquids that pond at the top of the chamber, and; (4) continued sidewall crystallization, now isolated from the chamber wall, produces silicic liquids with 63 wt % SiO₂ that increase the thickness and lowers the overall SiO₂ content of the upper silicic zone. It is suggested that the maximum SiO₂ content of 63% imposed on fractionation-generated magmas is due to a rheological barrier that prohibits the extraction of more silicic liquids from a crystal-liquid mush along the chamber wall.     

The Grayback Pluton: Magmatism in a Jurassic Back-Arc Environment, Klamath Mountains, Oregon

The Jurassic Grayback pluton was emplaced in a back-arc settingbehind a contemporaneous oceanic arc. Th\alphae main stage ofthe pluton consists of an early, reversely zoned tonalite togabbro that was intruded by synplutonic noritic and gabbroicmagmas. Late-stage activity was characterized by intrusion oftonalitic and granitic dikes, many of which contain mafic enclavesand hybrid zones. Most mafic rocks in the pluton are calc-alkaline,with characteristic magnesian clinopyroxene, calcic cores inplagioclase, and elemental abundances similar to H₂O-rich arcbasalts. However, some mafic rocks contain relatively Fe-richclinopyroxene, lack calcic cores in plagioclase, and are compositionallysimilar to evolved high-alumina tholeiite. Compositional variation in the main stage can be modeled inpart by fractional crystallization and crusted assimilationduring which parental calc-alkaline basalt evolved to graniticcompositions. Cumulates related to this process are representedby modally variable melagabbro and pyroxenite. Mixing of basalticand tonalitic magmas accounts for the compositions of most main-stageintermediate rocks, but mixing of basaltic and granitic magmaswas uncommon until late in the pluton's history. Oxygen, Sr and Nd isotopic data indicate that virtually allmain-stage magmas in the pluton contain a crustal component.Isotopic and trace element data further suggest that late-stagetonalitic dikes represent melts derived from older, metavolcanicarc crust Deep crustal contamination of main-stage rocks tookplace below the level of emplacement, probably in a magma-richzone where basalts ponded and mixed with crustal melts. The Grayback pluton illustrates the diversity of Jurassic back-arcmagmatism in the Klamath province and demonstrates that ancientmagmatism with arc-like features need not be situated in anarc setting. KEY WORDS: Grayback Pluton; Klamath Mountains; Oregon; back arc; crustal contamination ^*Corresponding author     

Melt Generation and Movement beneath Theistareykir, NE Iceland

A detailed study of the volume and composition of all the lavasfrom the Theistareykir segment of the Northern Volcanic Zoneof Iceland was designed to study basaltic melt generation andmovement beneath a spreading ridge. The trace element compositionsof the lavas are variable, and those of melt inclusions in olivine,clinopyroxene and plagioclase phenocrysts even more so. We showthat this variability can be produced by mixing instantaneousmelts produced by isentropic decompression of mantle whose initialpotential temperature is 1480°C, and that the calculatedvolume and composition of the average melt is consistent withgeophysical and petrological observations. Pressure and temperatureestimates suggest that the phenocrysts form in the upper mantle,at depths of 30–40 km, and trap melts formed at greaterdepths. Some mixing of the instantaneous melts occurs beforethe melt is trapped, and more mixing occurs before the lavasare erupted. A similar model can account for the compositionof melt inclusions from the FAMOUS area of the Mid-AtlanticRidge, and from the Gorda and Juan de Fuca Ridges. KEY WORDS: basalt; Iceland; melt inclusions; melting; ridges     

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

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

Trace element model studies of Nyanzian greenstone belts,western Kenya

The Archean greenstone belts of the Nyanzian System in western Kenya are composed principally of andesite with minor tholeiitic basalt and siliceous volcanics. The Nyanzian tholeiite is an intermediate-K tholeiite with a flat REE pattern. There are two chemically-distinct andesites: a low-K andesite (Andesite I) and a high-K andesite (Andesite II). The REE pattern of the Andesite II is enriched in light REE and depleted in heavy REE relative to Andesite I.Major and trace element calculations indicate an origin for the Nyanzian tholeiite by 35–40% equilibrium melting of a lherzolite source followed by 10% shallow fractional crystallization. Similar calculations best explain Andesite I and Andesite II by 20 and 5% melting, respectively, of an ecologite or garnet amphibolite source of Nyanzian tholeiite composition. The rhyolite may have formed either by 20–30% partial melting of a siliceous granulite or by 20–30% fractional crystallization of a granodiorite parent magma.With respect to total exposure areas, the Nyanzian volcanics have significantly less tholeiite and more Andesite and siliceous volcanics than other Archean greenstone belts. If these abundances are representative, two models are proposed to explain the anomalous abundances of Andesite and siliceous volcanics. The first model involves an Archaen upper mantle with a relatively low geothermal gradient beneath Kenya, while the second model involves a relatively cool mantle plume. Both models inhibit ascent of a significant amount of primary tholeiite to the surface and prevent formation of secondary tholeiite. Other Archean greenstone terranes with higher mantle geotherms or hotter mantle plumes would receive higher proportions of mafic and ultramafic magmas.