Crystal-Melt Separation and the Development of Isotopic Heterogeneities in Hybrid Magmas

If a magma is a hybrid of two (or more) isotopically distinctend-members, at least one of which is partially crystalline,separation of melt and crystals after hybridization will leadto the development of isotopic heterogeneities in the magmaas long as some of the pre-existing crystalline material (antecrysts)retains any of its original isotopic composition. This holdstrue whether the hybridization event is magma mixing as traditionallyconstrued, bulk assimilation, or melt assimilation. Once a magma-scaleisotopic heterogeneity is formed by crystal–melt separation,it is essentially permanent, persisting regardless of subsequentcrystallization, mixing, or equilibration events. The magnitudeof the isotopic variability resulting from crystal–meltseparation can be as large as that resulting from differentialcontamination, multiple isotopically distinct sources, or insitu isotopic evolution. In one model, a redistribution of one-thirdof the antecryst cargo yielded a crystal-enriched sample with⁸⁷Sr/⁸⁶Sr of 0·7058, whereas the complementary crystal-poorsample has ⁸⁷Sr/⁸⁶Sr of 0·7068. In other models, crystal-richsamples are enriched in radiogenic Sr. Isotopic heterogeneitiescan be either continuous (controlled by the modal distributionof crystals and melt) or discontinuous (when there is completeseparation of crystals and liquid). The first case may be exemplifiedby some isotopically zoned large-volume rhyolites, formed bythe eruptive inversion of a modally zoned magma chamber. Inthe latter case, the isotopic composition of any (for example)interstitial liquid will be distinct from the isotopic compositionof the bulk crystal fraction. The separation of such an interstitialliquid may explain the presence of isotopically distinct late-stageaplites in plutons. Crystal–melt separation provides anadditional option for the interpretation of isotopically zonedor heterogeneous magmas. This option is particularly attractivefor systems whose chemical variation is otherwise explicableby fractionation-dominated processes. Non-isotopic chemicalheterogeneities can also develop in this fashion. KEY WORDS: isotopic heterogeneity; zoning; hybrid magma; crystal separation; Sr isotopes; aplite; rhyolite     

Assimilation and diffusion during xenolith-magma interaction: a case study of the Variscan Karkonosze Granite, Bohemian Massif

Magmatic enclaves from the Rudolfov quarry near Liberec (Czech Republic) are interpreted to represent remnants of lamprophyric melt that intruded the Karkonosze granite at a stage at which the granite was not fully solidified. Based on the observation that larger enclaves are generally more circular than the smaller ones, we conclude that bigger blobs of mafic magma became more spherical during flow in the gravity field (sink or float). This flow is also interpreted to be responsible for the incorporation of mineral grains into the enclaves and may have facilitated the assimilation of granitic melt. Linear mixing trends on Harker diagrams for most network-forming and mainly slow-diffusing or fluid-immobile elements indicate such an assimilation process between granite and lamprophyre. In contrast, all fast-diffusing or fluid-mobile elements display scattered element distributions, implying that chemical diffusion also played a role. Pressure and temperature for this late magmatic stage are estimated at around 1 kbar and 500°C. These results suggest that two processes modified the composition of the enclaves in the Karkonosze granite: (1) assimilation (mechanical mixing) of granitic melt during the injection of the lamprophyric melt and the subsequent flow of the forming enclaves in the gravity field (responsible for the linear mixing trends) and (2) diffusion-controlled redistribution of elements between both solidifying rock types at the magmatic stage and/or due to late-stage magmatic fluids (responsible for the scattering and deviation from the linear mixing trends).     

Petrogenesis of granitoids from the Lachlan Fold Belt,southeastern Australia: The role of disequilibrium melting

S- and I-type granites from the Lachlan Fold Belt, southeastern Australia, have been investigated to assess the role of disequilibrium melting in their petrogenesis. Differences between the median initial εHf compositions of magmatic zircon populations and the host bulk-rock (ΔεHf^blk-zrc) range from −0.6 to +2.5 ε units, providing evidence for intra-sample (and hence inter-phase) Hf-isotopic heterogeneity. Linear variations on Harker diagrams and O and Hf isotope compositions of magmatic zircon preserved in many I- and S-type granites are inconsistent with assimilation or simple mixing hypotheses. In contrast, isotopic disequilibrium between the melt and a restite assemblage can explain the bulk-rock versus zircon differences observed in these samples.Assuming that magmatic zircon records the melt composition, differences between the bulk-rock εHf and εHf of magmatic zircon (ΔεHf^blk-zrc values) measured for I-type granites (0.4–2.5) can largely be explained by disequilibrium amphibole dehydration melting of meta-igneous protoliths that were either isotopically heterogenous at the time they were formed, or perfectly homogeneous before being aged in the crust for 0.4–1.0 billion years prior to partial melting. The Currowong Suite exhibits petrographic features and preserves geochemical and isotopic compositions that do not lend themselves to simple restite model or magma mixing explanations; however, these observations could be explained by the restite unmixing of magma batches generated from a single source rock if, as modelling has suggested, separate batches contain different melt compositions.By investigating the application of disequilibrium melting to granite genesis, this study demonstrates that isotopic heterogeneity at various sampling scales should actually be expected for the production of granites from a single source, rather than necessitating the involvement of multiple sources and mixing processes. As a result great care should be taken in the interpretation of isotope data from granitic bulk-rocks or their zircons.     

Nature and origin of A-type granites with particular reference to southeastern Australia

In the Lachlan Fold Belt of southeastern Australia, Upper Devonian A-type granite suites were emplaced after the Lower Devonian I-type granites of the Bega Batholith. Individual plutons of two A-type suites are homogeneous and the granites are characterized by late interstitial annite. Chemically they are distinguished from I-type granites with similar SiO₂ contents of the Bega Batholith, by higher abundances of large highly charged cations such as Nb, Ga, Y, and the REE and lower Al, Mg and Ca: high Ga/Al is diagnostic. These A-type suites are metaluminous, but peralkaline and peraluminous A-type granites also occur in Australia and elsewhere. Partial melting of felsic granulite is the preferred genetic model. This source rock is the residue remaining in the lower crust after production of a previous granite. High temperature, vapour-absent melting of the granulitic source generates a low viscosity, relatively anhydrous melt containing F and possibly Cl. The framework structure of this melt is considerably distorted by the presence of these dissolved halides allowing the large highly charged cations to form stable high co-ordination structures. The high concentration of Zr and probably other elements such as the REE in peralkaline or near peralkaline A-type melts is a result of the counter ion effect where excess alkali cations stabilize structures in the melt such as alkali-zircono-silicates. The melt structure determines the trace element composition of the granite. Separation of a fluid phase from an A-type magma results in destabilization of co-ordination complexes and in the formation of rare-metal deposits commonly associated with fluorite. At this stage the role of Cl in metal transport is considered more important than F.     

The adaptation of Pearce element ratio diagrams to complex high silica systems

Pearce element ratios (PERs, of Pearce 1968) express geochemical data in a form where variations in absolute compositions of an igneous suite can be evaluated. Generally the denominator value in the ratio is taken as a major element abundance, but it is argued here that Zr provides a more suitable choice. Zr remains incompatible in magmatic systems up to 68 wt.% SiO₂ because zircon fractionation can be suppressed by high melt temperatures and increased volatile contents. The use of Zr thus permits PER modelling to be extended to much higher levels of silica than previously investigated. However, such systems are more complex than those just involving simple basaltic magmas. Besides fractionation, the processes of magma mixing, combined assimilation and fractional crystallization, and the initial degree of partial melting in the mantle source must also be considered. To distinguish and evaluate these processes a set of example suites are investigated from a complex synextensional calc-alkaline province in the western USA. Samples within most individual suites can be modelled by fractionation, however a significant trend orthogonal to the main fractionation vector is also apparent, and open system processes are inferred. Successful modelling is achieved on an inter-suite basis using diagrams with axis functions of ([4(Ca+Na)+0.5(Fe+Mg)]/Zr versus (Si+Al)/Zr). Potential open system evolution paths between mafic end members and crustal contaminants are also displayed and evaluated on these same diagrams. The encouraging results suggest that such PER diagrams may be employed as a versatile tool for investigating the systematics of related igneous suites over a wide area.     

Some Thermal Constraints on Crustal Assimilation during Fractionation of Hydrous, Mantle-derived Magmas with Examples from Central Alpine Batholiths

We provide a model for the fractional crystallization of hydrousmantle-derived magma to form calc-alkaline plutons, based uponmass balance for geological examples of fractionation sequencesin the lower continental crust. This is complemented by a thermalmodel for the heat budget obtained from a projected phase diagramand thermodynamic data. Fractional crystallization (FC) andassimilation–fractional crystallization (AFC) paths havebeen calculated with these models and the mass ratio of assimilationto crystallization as a function of parent magma type and temperature,crustal rock fertility and temperature, and mechanism of assimilation,have been determined. When these results are combined with F(melt fraction) and r (ratio of mass assimilated/crystallized)values evaluated from geochemical data then new information,not available with the methods separately, can be deduced. Thisincludes when and at what depth and temperature in the crustthe assimilation took place, as well as the likely parent magmatype and temperature of the assimilant. Our results are presentedin simple graphical fashion to facilitate future studies thatexamine the evolution of individual calc-alkaline plutons andthe mechanisms of crustal contamination, and to improve meltmodels involving hydrous magma in volcanic arcs and in the lowercontinental crust KEY WORDS: assimilation; hydrous mantle magma; thermal models; fractional crystallization; magma mixing; Alpine batholiths; Adamello; Bergell     

Chemical versus Temporal Controls on the Evolution of Tholeiitic and Calc-alkaline Magmas at Two Volcanoes in the Alaska-Aleutian Arc

The Alaska–Aleutian island arc is well known for eruptingboth tholeiitic and calc-alkaline magmas. To investigate therelative roles of chemical and temporal controls in generatingthese contrasting liquid lines of descent we have undertakena detailed study of tholeiitic lavas from Akutan volcano inthe oceanic Aleutian arc and calc-alkaline products from Aniakchakvolcano on the continental Alaskan Peninsula. The differencesdo not appear to be linked to parental magma composition. TheAkutan lavas can be explained by closed-system magmatic evolution,whereas curvilinear trace element trends and a large range in⁸⁷Sr/⁸⁶Sr isotope ratios in the Aniakchak data appear to requirethe combined effects of fractional crystallization, assimilationand magma mixing. Both magmatic suites preserve a similar rangein ²²⁶Ra–²³⁰Th disequilibria, which suggests that thetime scale of crustal residence of magmas beneath both thesevolcanoes was similar, and of the order of several thousandyears. This is consistent with numerical estimates of the timescales for crystallization caused by cooling in convecting crustalmagma chambers. During that time interval the tholeiitic Akutanmagmas underwent restricted, closed-system, compositional evolution.In contrast, the calc-alkaline magmas beneath Aniakchak volcanounderwent significant open-system compositional evolution. Combiningthese results with data from other studies we suggest that differentiationis faster in calc-alkaline and potassic magma series than intholeiitic series, owing to a combination of greater extentsof assimilation, magma mixing and cooling. KEY WORDS: uranium-series; Aleutian arc; magma differentiation; time scales     

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     

Melt Inclusions in Primitive Olivine Phenocrysts: the Role of Localized Reaction Processes in the Origin of Anomalous Compositions

Melt inclusions are small portions of liquid trapped by growingcrystals during magma evolution. Recent studies of melt inclusionshave revealed a large range of unusual major and trace elementcompositions in phenocrysts from primitive mantle-derived magmaticrocks [e.g. in high-Fo olivine (Fo > 85 mol %), spinel, high-Anplagioclase]. Inclusions in phenocrysts crystallized from moreevolved magmas (e.g. olivine Fo < 85 mol %), are usuallycompositionally similar to the host lavas. This paper reviewsthe chemistry of melt inclusions in high-Fo olivine phenocrystsfocusing on those with anomalous major and trace element contentsfrom mid-ocean ridge and subduction-related basalts. We suggestthat a significant portion of the anomalous inclusion compositionsreflects localized, grain-scale dissolution–reaction–mixing(DRM) processes within the magmatic plumbing system. The DRMprocesses occur at the margins of primitive magma bodies, wheremagma is in contact with cooler wall rocks and/or pre-existingsemi-solidified crystal mush zones (depending on the specificenvironment). Injection of hotter, more primitive magma causespartial dissolution (incongruent melting) of the mush-zone phases,which are not in equilibrium with the primitive melt, and mixingof the reaction products with the primitive magma. Localizedrapid crystallization of high-Fo olivines from the primitivemagma may lead to entrapment of numerous large melt inclusions,which record the DRM processes in progress. In some magmaticsuites melt inclusions in primitive phenocrysts may be naturallybiased towards the anomalous compositions. The occurrence ofmelt inclusions with unusual compositions does not necessarilyimply the existence of new geologically significant magma typesand/or melt-generation processes, and caution should be exercisedin their interpretation. KEY WORDS: melt inclusions; olivine; geochemistry; mush zones; MORB; subduction-related magmas     

Evolution of the Kap Edvard Holm Complex: a Mafic Intrusion at a Rifted Continental Margin

The Kap Edvard Holm Layered Series forms part of the East GreenlandTertiary Province, and was emplaced at shallow crustal level(at depths corresponding to a pressure of 1–2 kbar) duringcontinental break-up. It consists of two suites: a gabbro suitecomprising olivine and oxide gabbros, leucocratic olivine gabbrosand anorthosites, and a suite of wehrlites that formed fromthe intrusion of the gabbros during their solidification bya hydrous, high-MgO magma. Ion microprobe analyses of clinopyroxenereveal chemical contrasts between the parental melt of the wehrlitesuite and that of the gabbro suite. Thin sills (1–2 mthick) of the wehrlite suite, however, have clinopyroxene compositionssimilar to the gabbro suite, and were formed by interactionwith interstitial melts from the host layered gabbros. All evolvedmembers of the gabbro suite have elevated Nd, Zr and Sr concentrationsand Nd/Yb ratios, relative to the melt parental to the gabbrosuite. These characteristics are attributed to establishmentof a magma chamber at depths corresponding to a pressure of10 kbar, where melts evolved before injection into the low-pressuremagma chamber. Anorthosites of the gabbro suite are believedto have crystallized from such injections. The melts becamesupersaturated in plagioclase by the pressure release that followedtransportation to the low-pressure magma chamber after initialfractionation at 10 kbar. The most evolved gabbros formed bysubsequent fractionation within the low-pressure magma chamber.Our results indicate that high-pressure fractionation may beimportant in generating some of the lithological variationsin layered intrusions. KEY WORDS: fractionation; ion microprobe; layered intrusions; rift processes; trace elements ^*Corresponding author.     

Magma mixing in the San Francisco Volcanic Field,AZ

A wide variety of rock types are present in the O'Leary Peak and Strawberry Crater volcanics of the Pliocene to Recent San Francisco Volcanic Field (SFVF), AZ. The O'Leary Peak flows range from andesite to rhyolite (56–72 wt % SiO₂) and the Strawberry Crater flows range from basalt to dacite (49–64 wt % SiO₂). Our interpretation of the chemical data is that both magma mixing and crustal melting are important in the genesis of the intermediate composition lavas of both suites. Observed chemical variations in major and trace elements can be modeled as binary mixtures between a crustal melt similar to the O'Leary dome rhyolite and two different mafic end-members. The mafic end-member of the Strawberry suite may be a primary mantle-derived melt. Similar basalts have also been erupted from many other vents in the SFVF. In the O'Leary Peak suite, the mafic end-member is an evolved (low Mg/(Mg+ Fe)) basalt that is chemically distinct from the Strawberry Crater and other vent basalts as it is richer in total Fe, TiO₂, Al₂O₃, MnO, Na₂O, K₂O, and Zr and poorer in MgO, CaO, P₂O₅, Ni, Sc, Cr, and V. The derivative basalt probably results from fractional crystallization of the more primitive, vent basalt type of magma. This evolved basalt occurs as xenolithic (but originally magmatic) inclusions in the O'Leary domes and andesite porphyry flow. The most mafic xenolith may represent melt that mixed with the O'Leary dome rhyolite resulting in andesite preserved as other xenoliths, a pyroclastic unit (Qoap), porphyry flow (Qoaf) and dacite (Darton Dome) magmas. Thermal constraints on the capacity of a melt to assimilate (and melt) a volume of solid material require that melt mixing and not assimilation has produced the observed intermediate lavas at both Strawberry Crater and O'Leary Peak. Textures, petrography, and mineral chemistry support the magma mixing model. Some of the inclusions have quenched rims where in contact with the host. The intermediate rocks, including the andesite xenoliths, contain xenocrysts of quartz, olivine and oligoclase, together with reversely zoned plagioclase and pyroxene phenocrysts. The abundance of intermediate volcanic rocks in the SFVF, as observed in detail at O'Leary Peak and Strawberry Crater, is due in part to crustal recycling, the result of basalt-driven crustal melting and the subsequent mixing of the silicic melts with basalts and derivative magmas.     

Rapid Change of Lava Composition from 1998 to 2002 at Piton de la Fournaise (Reunion) Inferred from Pb Isotopes and Trace Elements: Evidence for Variable Crustal Contamination

After an unusually long quiet period of nearly 6 years, in 1998the Piton de la Fournaise volcano started a new cycle of intensevolcanic activity. We report geochemical data on the first nineevents (53 samples), from the long-lived initial eruption (sixand a half months) of 1998 to the high-flux picritic eruptionof January 2002. Pb isotopes and trace elements display systematic,coupled variations, which are mostly confined to the beginningand the end of the period. Two well-defined binary mixing trendsare shown by Pb–Pb and Pb–trace element relationships.These trends indicate a change of end-member components betweenMarch and June 2001 that coincides with the transition fromsteady-state basalts to picrites. A three-component mixing modelinvolving a homogeneous plume and two contaminants successfullyexplains the data. The Pb–Pb relationship requires thattwo mixing processes occur successively: plume-derived magmainteracts first with altered oceanic crust, and the resultinghybrid product then interacts at shallower level with the oldlavas constituting the base of the volcanic edifice. Assimilationof edifice material decreased continuously from 1998 to 2002,whereas assimilation of oceanic crust drastically increasedduring the late-stage picritic eruption. These results suggestthat picrites may have resided for an unusually long time atan oceanic crustal level before ascending rapidly through thevolcanic edifice with little interaction with channel walls. KEY WORDS: assimilation; lead isotopes; picrites; Piton de la Fournaise; trace elements     

Assimilation and Fractional Crystallization Controlled by Transport Process of Crustal Melt: Implications from an Alkali Basalt-Dacite Suite from Rishiri Volcano, Japan

Mechanisms of fractional crystallization with simultaneous crustalassimilation (AFC) are examined for the Kutsugata and Tanetomilavas, an alkali basalt–dacite suite erupted sequentiallyfrom Rishiri Volcano, northern Japan. The major element variationswithin the suite can be explained by boundary layer fractionation;that is, mixing of a magma in the main part of the magma bodywith a fractionated interstitial melt transported from the mushyboundary layer at the floor. Systematic variations in SiO₂ correlatewith variations in the Pb, Sr and Nd isotopic compositions ofthe lavas. The geochemical variations of the lavas are explainedby a constant and relatively low ratio of assimilated mass tocrystallized mass (‘r value’). In the magma chamberin which the Kutsugata and Tanetomi magmas evolved, a strongthermal gradient was present and it is suggested that the marginalpart of the reservoir was completely solidified. The assimilantwas transported by crack flow from the partially fused floorcrust to the partially crystallized floor mush zone throughfractures in the solidified margin, formed mainly by thermalstresses resulting from cooling of the solidified margin andheating of the crust. The crustal melt was then mixed with thefractionated interstitial melt in the mushy zone, and the mixedmelt was further transported by compositional convection tothe main magma, causing its geochemical evolution to be characteristicof AFC. The volume flux of the assimilant from the crust tothe magma chamber is suggested to have decreased progressivelywith time (proportional to t^–1/2), and was about 3 x 10^–2m/year at t = 10 years and 1 x 10^–2 m/year at t = 100years. It has been commonly considered that the heat balancebetween magmas and the surrounding crust controls the couplingof assimilation and fractional crystallization processes (i.e.absolute value of r). However, it is inferred from this studythat the ratio of assimilated mass to crystallized mass canbe controlled by the transport process of the assimilant fromthe crust to magma chambers. KEY WORDS: assimilation and fractional crystallization; mass balance model; magma chamber; melt transport; Pb isotope     

Inclusions in Three S-Type Granites from Southeastern Australia

The Jillamatong Granodiorite is one of the most mafic S-typegranites in the Kosciusko regidn and is typical of widely distributed,cordierite-bearing S-type granites in the Lachlan Fold Beltof southeastern Australia. The Koetong and Granya Adamellitesbelong to the Koetong Suite of the Corryong Batholith and arerare examples in the Lachlan Fold Belt of granites that containprimary muscovite. Although subtle differences can be found,inclusions within the Jillamatong Granodiorite and the KoetongSuite are broadly similar despite the fact that the JillamatongGranodiorite belongs to a different and distinct suite (theBullenbalong Suite). Mica-rich schistose and micTogranular inclusionsdominate but other types occur, including foliated quartzofeldspathicvarieties, calcsilicates, quartzites, and pure quartz types.The total abundance of all inclusion types in each granite studiedis less than 5.1% although abundance varies from one graniteto another. All inclusions are believed to have been derived from metasedimentaryor modified metasedimentary lithologies and all inclusions,except some quartzites, were entrained at depth where the hostgranite magmas were generated by partial melting of heterogeneoussedimentary sources. The inclusions are restite but most arenot complementary to the melt component of the magma now representedby the host granite. They represent fragments from differentrefractory lithologies of a complex metasedimentary source andbecause their compositions and mineral assemblages were unsuitablefor the generation of large quantities of granite melt, theydid not melt or were melted only to small and variable extents(less than the rheological critical melt percentage of Arzi,1978). Such lithologies remained physically coherent and retainedtheir separation from the host granite magma during ascent.Lithologies that did melt extensively were physically disaggregatedand are not represented among the inclusions. Since the inclusions do not represent complementary restitecontrolling compositional variation among the host granites,their compositions cannot be used to precisely estimate thebulk compositions of the source rocks. However, the different,source-rock derived, inclusion types collectively provide informationregarding the lithologies present in the source and hence thegeneral character of the source terranes. The dominance of schistoseand microgranular inclusions in the Jillamatong Granodioriteand the Koetong Suite indicates that pelitic and quartzofeldspathiccompositions are the two dominant components in the source terranes. Inclusions of the same type from the two suites are broadlysimilar but different in detail. Inclusions reflect the mineralogicaland geochemical characteristics of their host granites and thereare textural differences between microgranular inclusions ofthe two suites examined. The differences reflect subtle butsignificant contrasts in source materials, the conditions prevailingduring partial melting and the history of emplacement and crystallizationof the host magmas.     

Formation and Modification of the Shallow Sub-continental Lithospheric Mantle: a Review of Geochemical Evidence from Ultramafic Xenolith Suites and Tectonically Emplaced Ultramafic Massifs of Western and Central Europe

The petrology and geochemistry of shallow continental lithosphericmantle (SCLM) can be studied via (1) tectonically emplaced ultramaficmassifs and (2) mantle xenoliths entrained in alkaline magmas.Data from these two separate sources are used to identify processesthat have formed and modified the SCLM. In western and centralEurope where the continental crust consolidated in Phanerozoictimes, both sources of information are available for study.Rock types found in ultramafic massifs in Europe are generallysimilar to those found in ultramafic xenolith suites. The mostfrequent lithology is anhydrous spinel lherzolite, grading towardsharzburgite. Massifs reveal pyroxenite layering, harzburgitebands and cross-cutting mafic and ultramafic dykes. The PhanerozoicEuropean SCLM xenoliths and massifs show broad mineralogicaland chemical similarities to Phanerozoic continental spinelperidotites world-wide. The main process that controls the geochemistryof the SCLM is depletion by removal of basaltic melt. Differencesfrom this norm reflect significantly different processes inthe SCLM, such as interaction with melts and fluids. Such processesprobably gave rise to hornblendite veins and pyroxenite layers,although the latter have also been interpreted as recycled oceaniccrust. Rare earth element data for whole-rock peridotites andtheir constituent clinopyroxenes show a variety of patterns,including light rare earth element (LREE) depletion as a resultof removal of basaltic melt, LREE enrichment caused by metasomatism,and U-shaped REE patterns that are probably due to interactionwith carbonatite melts. Extended mantle-normalized incompatibletrace element patterns for whole rocks show enrichment in Rband Ba in peridotites considered to have been subduction-metasomatized,whereas those considered to be carbonate-metasomatized havestrong negative anomalies in Zr, Nb and Hf. Mantle amphibolesare strongly enriched in LREE when found in veins, but can beLREE depleted if they are interstitial. Radiogenic isotope ratiosfor xenoliths and massifs largely overlap, although the xenolithsshow a significant clustering around a ‘plume-component’identical to the Neogene alkaline magmatism of Europe. Thiscomponent is lacking in the massifs, most of which were emplacedinto the crust before the onset of Neogene plume activity. Infiltrationof carbonatite melts is observed petrographically in some xenolithsand evidenced by low Ti/Eu ratios in bulk rocks, but is veryrare. The effect of passage of hydrous fluids from subductingslabs is also seen in some suites and massifs, being exhibitedmainly as unusual Sr and Pb isotope ratios, although enrichmentin K, Rb and Ba, and the presence of modal phlogopite, may alsopoint to subduction-metasomatism. KEY WORDS: peridotites; xenoliths; orogenic massifs; Europe     

Geochemical Constraints on Possible Subduction Components in Lavas of Mayon and Taal Volcanoes, Southern Luzon, Philippines

Mayon is the most active volcano along the east margin of southernLuzon, Philippines. Petrographic and major element data indicatethat Mayon has produced a basaltic to andesitic lava seriesby fractional crystallization and magma mixing. Trace elementdata indicate that the parental basalts came from a heterogeneousmantle source. The unmodified composition of the mantle wedgeis similar to that beneath the Indian Ocean. To this mantlewas added a subduction component consisting of melt from subductedpelagic sediment and aqueous fluid dehydrated from the subductedbasaltic crust. Lavas from the highly active Taal Volcano onthe west margin of southern Luzon are compositionally more variablethan Mayon lavas. Taal lavas also originated from a mantle wedgemetasomatized by aqueous fluid dehydrated from the subductedbasaltic crust and melt plus fluid derived from the subductedterrigenous sediment. More sediment is involved in the generationof Taal lavas. Lead isotopes argue against crustal contamination.Some heterogeneity of the unmodified mantle wedge and differencesin whether the sediment signature is transferred into the lavasource through an aqueous fluid or melt phase are needed toexplain the regional compositional variation of Philippine arclavas. KEY WORDS: Mayon Volcano; Philippines; sediment melt; subduction component; Taal Volcano     

Partial Melting and Assimilation of Dolomitic Xenoliths by Mafic Magma: the Ioko-Dovyren Intrusion (North Baikal Region, Russia)

A petrological study was carried out on Mg-skarn-bearing dunitecumulates that are part of the Neo-Proterozoic Ioko-Dovyrenintrusion (North Baikal region, Russia). Skarn xenoliths containbrucite pseudomorphs after periclase, forsterite and Cr-poorspinel. Fine-grained forsterite–spinel skarns occur withthe brucite skarns or as isolated schlieren. Field relationshipsreveal that the Mg-skarns formed from silica-poor dolomiticxenoliths by interaction with the mafic magma of the Ioko-Dovyrenintrusion. Rapid heating of dolomitic xenoliths by the maficmagma caused the decomposition of dolomite into calcite + periclase,releasing much CO₂. Further heating quantitatively melted thecalcite. A periclase-rich restite was left behind after extractionof the low-density, low-viscosity calcite melt. The extractedcalcite melt mixed with the surrounding mafic melt. This resultedin crystallization of olivine with CaO contents up to 1·67wt %. A local decrease in the silica concentration stabilizedCaAl₂SiO₆-rich clinopyroxene. Brucite/periclase-free forsterite–spinelskarns probably originated by crystallization from the maficmelt close to the xenoliths at elevated fO₂. The high fO₂ wascaused by CO₂-rich fluids released during the decompositionof the xenoliths. The above case study provides the first evidencefor partial melting of dolomite xenoliths during incorporationby a mafic magma. KEY WORDS: dunite; dolomite assimilation; partial melting     

Trace Element Geochemical Effects of Integrated Melt Extraction and 'Shaped' Melting Regimes

The mixing (integration) of liquids obtained as different massfractions of partial melting from source material of the samebulk composition, travelling along different mantle flow-linesthrough a melting regime, can result in deficiencies in therelative concentrations of those incompatible elements whosebulk distribution coefficients are numerically approximatelyequal to the average mass fraction of melt extracted from thetotal source material involved in the provision of the mixedmelts. These deficiencies can be very substantial, exceeding50% of the concentration which would have been expected to bepresent in the liquid if that same average mass fraction ofmelt had been extracted from the whole melting regime by simpleequilibrium or accumulated perfect fractional partial melting.The size of the deficit varies with the shape and plan-formof the melting region, and can be greatly reduced by subsequentperfect fractional crystallization of that liquid. Discriminationis increased between all elements whose distribution coefficientsare numerically smaller than the average mass fraction of partialmelt extracted from the whole region. These effects can leadto steepening of chondrite-normalized REE patterns and to apparentselective light rare earth enrichment in liquid and source. KEY WORDS: melt integration; shaped melting regimes; trace elements; numerical modelling     

Source component mixing controls the variability in Cu and Au endowment along the strike of the Eastern Andean Cordillera in Peru

Mississippian arc magmatic suites of the Au-rich Pataz and Cu-dominated Montañitas regions in Peru reveal distinct modes of magmatic-hydrothermal petro- and metallogenesis. The distinction is remarkable due to their broad contemporaneity (336–322 Ma), arc-parallel position, and close distance (<?50 km) to each other. In both arc regions, petrography, geochemistry, and the tectonic setting of magmatic suites suggest a rapid switch from syn-collisional/compressional to post-collisional/extensional (with ‘A₂-type’ signature) emplacement regime. Rocks of the Au-rich Pataz region originate from mixed sources with a contribution from the mantle (εHf?>?0 and δ¹⁸O of ~?5.3‰) and assimilated old crust (variously low εHf and δ¹⁸O >?5.3‰). The ultimate source of Au in the mineralised Pataz batholith was oxidised (fO₂ at FMQ buffer; based on zircon trace chemistry) and alkali-, LILE- and HFSE-enriched, most likely represented by the metasomatised mantle. The syn-extensional emplacement of the relatively reduced (ΔFMQ?<?0), but unmineralised, A₂-type suite involved assimilation of reduced crust. Associated, reduced, magmatic-hydrothermal fluids infiltrated the Au-bearing batholith suite and effectively mobilised and transported and concentrated Au. In the Montañitas region, rocks are oxidised (ΔFMQ?>?0) and dominantly mantle derived without significant incorporation of crustal material. Samples from the Cu-mineralised suites indicate the additional contribution of a δ¹⁸O <?5.3‰ source, potentially melted layer-2 gabbro. In addition, the elevated whole-rock La/Yb and Sr/Y ratios are compatible with minor addition of slab-derived material, which may have enhanced Cu endowment in this region. Late-magmatic, oxidised fluids derived from the younger A₂-type suite controlled Cu mobilisation and concentration, while Au behaved largely refractory. In general terms, it is postulated that source mixing in continental arcs is a first-order control of contrasting Cu and Au endowment and that sequential intrusion processes facilitate late-magmatic-hydrothermal mobilisation and concentration of specific metal assemblages.     

A zircon U-Pb study of metaluminous (I-type) granites of the Lachlan Fold Belt,southeastern Australia: implications for the high/low temperature classification and magma differentiation processes

Following seminal studies in the Lachlan Fold Belt (southeastern Australia), it has become almost axiomatic that metaluminous granites derive from infracrustal precursors, whereas strongly peraluminous plutons have metasedimentary or supracrustal sources, as reflected in the I- and S-type designation. Recently, zircon saturation thermometry has been used to further subdivide I-type granites into high- and low-temperature categories. That low-temperature I-type granites evolved by restite separation from magmas generated in the zircon stability field is implicit in this classification. To explore this hypothesis, we report an ion microprobe U-Pb (zircon) study into three hallmark ‘low-temperature’ Lachlan Fold Belt I-type suites. The combined patterns of zircon age inheritance and bulk rock Zr trends suggest that each suite formed from magmas that were initially zircon-undersaturated, and that fractional crystallisation, not restite unmixing, was the dominant differentiation process. The low temperature status presently applied to these rocks cannot therefore be justified. The inherited zircons in these I-type granites reflect melting and assimilation of metasedimentary rock, and testify to a supracrustal source component. Electronic Supplementary Material Supplementary material is available for this article at