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     

Evolution and Genesis of Magmas from Vico Volcano, Central Italy: Multiple Differentiation Pathways and Variable Parental Magmas

Vico volcano has erupted potassic and ultrapotassic magmas,ranging from silica-saturated to silica-undersaturated types,in three distinct volcanic periods over the past 0·5Myr. During Period I magma compositions changed from latiteto trachyte and rhyolite, with minor phono-tephrite; duringPeriods II and III the erupted magmas were primarly phono-tephriteto tephri-phonolite and phonolite; however, magmatic episodesinvolving leucite-free eruptives with latitic, trachytic andolivine latitic compositions also occurred. In Period II, leucite-bearingmagmas (⁸⁷Sr/⁸⁶Sr_initial = 0·71037–0·71115)were derived from a primitive tephrite parental magma. Modellingof phonolites with different modal plagioclase and Sr contentsindicates that low-Sr phonolitic lavas differentiated from tephri-phonoliteby fractional crystallization of 7% olivine + 27% clinopyroxene+ 54% plagioclase + 10% Fe–Ti oxides + 4% apatite at lowpressure, whereas high-Sr phonolitic lavas were generated byfractional crystallization at higher pressure. More differentiatedphonolites were generated from the parental magma of the high-Srphonolitic tephra by fractional crystallization of 10–29%clinopyroxene + 12–15% plagioclase + 44–67% sanidine+ 2–4% phlogopite + 1–3% apatite + 7–10% Fe–Tioxides. In contrast, leucite-bearing rocks of Period III (⁸⁷Sr/⁸⁶Sr_initial= 0·70812–0·70948) were derived from a potassictrachybasalt by assimilation–fractional crystallizationwith 20–40% of solid removed and r = 0·4–0·5(where r is assimilation rate/crystallization rate) at differentpressures. Silica-saturated magmas of Period II (⁸⁷Sr/⁸⁶Sr_initial= 0·71044–0·71052) appear to have been generatedfrom an olivine latite similar to some of the youngest eruptedproducts. A primitive tephrite, a potassic trachybasalt andan olivine latite are inferred to be the parental magmas atVico. These magmas were generated by partial melting of a veinedlithospheric mantle sources with different vein–peridotite/wall-rockproportions, amount of residual apatite and distinct isolationtimes for the veins. KEY WORDS: isotope and trace element geochemistry; polybaric differentiation; veined mantle; potassic and ultrapotassic rocks; Vico volcano; central Italy     

Quantification of Crustal Contamination in Open Magmatic Systems

The DePaolo (1981a, Earth Planet. Sci. Lett. 53, 189–202)equations for assimilation with fractional crystallization (AFC)are extended and solved to yield directly the fraction of crustassimilated during AFC with or without magma replenishment orrecharge. Errors in the computed crust/magma ratio are alsopresented. Using graphical methods and a sufficient number ofelements no assumptions need be made about the value of theratios r (= rate of assimilation/rate of fractional crystallization)and ß (= rate of recharge/rate of assimilation); infact, the method yields independent estimates of these ratiosin addition to the crust/magma ratio. Thus the average relativesizes of the fluxes of wall-rock melt, replenishing magma, andfractionating phases are known and can be incorporated in abudget for the whole magma-crust system. The method for calculatingthe crust/magma ratio is extended to encompass variable valuesof r, ß, and bulk distribution coefficient (D). Simple(bulk) mixing is effectively a special case of AFC where ßor r and/or D = 0. Only for highly incompatible elements (D<01)do bulk mixing calculations approximate the true crust/magmaratio if AFC processes operated. For more compatible elements(e.g., oxygen) bulk mixing calculations considerably overestimatethe crust/magma ratio if r and ß are constant. Thecomplications of compositional stratification and diffusionin magma chambers are considered qualitatively. Two examples illustrate the application of the methods developedhere. For the upper zone of the Lille Kufjord instrusion innorthern Norway, an example of mid-crustal AFC without magmarecharge, either r = 0.04 and the crust/magma ratio is 0.04,or r = 0.08 and the crust/magma ratio is 0.06. For lavas ofthe Andean Central Volcanic Zone, an example of deep AFC withpossible recharge, r = 0.15, ß = 3.2, and the crust/magmaratio is 0.16.     

Polybaric Evolution of Calc-alkaline Magmas from Nisyros, Southeastern Hellenic Arc, Greece

The lavas of Nisyros were erupted between about 0?2 m.y B.P.and 1422 A.D., and range in composition from basaltic andesiteto rhyodacite. Most were erupted prior to caldera collapse (exactdate unknown), and the post-caldera lavas are petrographically(presence of strongly resorbed phenocrysts) and chemically (lowerTiO₂ K₂O, P₂O₅, and LIL elements) distinct from the pre-calderalavas. The pre-caldera lavas do not form a continuous seriessince lavas with SiO₂ contents between 60 and 66 wt.% are absent.Nevertheless, major element variations demonstrate that fractionalcrystalliz ation (involving removal of olivine, dinopyroxene,plagioclase, and Fe-Ti oxide from the basaltic andesites andandesites and plagioclase, clinopyroxene, hypersthene, Ti-magnetite,ilmenite, apatite, and zircon from the dacites and rhyodacites)played a major role in the evolution of the pre-caldera lavas.Several lines of evidence indicate that other processes werealso important in magma evolution: (1) Quantitative modelingof major element data shows that phenocryst phases of unlikelycomposi tion or unrealistic assemblages of phenocryst phasesare required to relate the dacites and rhyodacites to the basalticandesites and andesites; (2) The proportions of olivine andclinopyroxene required in quantitative models for the initialstages of evolution differ from those observed petrographicallyand this is not likely to reflect either differential ratesof crystal settling or the curvature of cotectics along whichliquids of basaltic andesite to andesite composition lie; (3)The concentrations of Rb, Cs, Ba, La, Sm, Eu, and Th in therhyod.acites are too high for these lavas to be related to thedacites by fractional crystallization alone; and (4) ⁸⁷Sr/⁸⁶Srratios for the andesites and rhyodacites are higher than thosefor the basaltic andesites and dacites, respectively. It isshown that fractional crystallization was accompanied by assimilation,and that magma mixing played a minor role (if any) in the evolutionof the pre-caldera lavas. Trace element and isotopic data indicatethat the andesites evolved from the basaltic andesites by AFCinvolving average crust or upper crust, whereas the rhyodacitesevolved from the dacites by AFC involving lower crust. Additionalevidence for polybaric evolution is provided by the occurrenceof distinct Ab-rich cores of plagioclase phenocrysts in thedacites and rhyodacites, which record a period of high pressurecrystallization, and by the occurrence of both normal and reverse-zonedphenocrysts in the basaltic andesites and andesites. Furthermore,calculated pressures of crystallization are {small tilde}8 kbfor the dacites and rhyodacites and 3?5–4 kb for the basalticandesites and andesites. It is concluded that the dacites andrhyodacites evolved via AFC from basaltic andesites and andesiteslargely in chambers sited near the base of the crust whereasthe basaltic andesites and andesites mostly evolved in chamberssited at mid-crustal levels. Eruption from different chambersexplains the compositional gap in the chemistry of the pre-calderalavas since eruptive products represent a more or less randomsampling of residual liquids which separate (via filter pressing)from bodies of crystallizing magma at various depths. Magmamixing was important in the evolution of the post-caldera lavas,but geochemical data require that these magmas evolved fromparental magmas which were derived from a more refractory sourcethan the parental magmas to the pre-caldera lavas. ^*Present address: Netherlands Energy Research Foundation (ECN), P.O. Box 1, 1755 ZG Petten, The Netherlands     

Rates of Thermal and Chemical Evolution of Magmas in a Cooling Magma Chamber: a Chronological and Theoretical Study on Basaltic and Andesitic Lavas from Rishiri Volcano, Japan

Rates of magmatic processes in a cooling magma chamber wereinvestigated for alkali basalt and trachytic andesite lavaserupted sequentially from Rishiri Volcano, northern Japan, bydating of these lavas using ²³⁸U–²³⁰Th radioactive disequilibriumand ¹⁴C dating methods, in combination with theoretical analyses.We obtained the eruption age of the basaltic lavas to be 29·3± 0·6 ka by ¹⁴C dating of charcoals. The eruptionage of the andesitic lavas was estimated to be 20·2 ±3·1 ka, utilizing a whole-rock isochron formed by U–Thfractionation as a result of degassing after lava emplacement.Because these two lavas represent a series of magmas producedby assimilation and fractional crystallization in the same magmachamber, the difference of the ages (i.e. 9 kyr) is a timescaleof magmatic evolution. The thermal and chemical evolution ofthe Rishiri magma chamber was modeled using mass and energybalance constraints, as well as quantitative information obtainedfrom petrological and geochemical observations on the lavas.Using the timescale of 9 kyr, the thickness of the magma chamberis estimated to have been about 1·7 km. The model calculationsshow that, in the early stage of the evolution, the magma cooledat a relatively high rate (>0·1°C/year), and thecooling rate decreased with time. Convective heat flux fromthe main magma body exceeded 2 W/m² when the magma was basaltic,and the intensity diminished exponentially with magmatic evolution.Volume flux of crustal materials to the magma chamber and rateof convective melt exchange (compositional convection) betweenthe main magma and mush melt also decreased with time, from 0·1 m/year to 10^–3 m/year, and from 1 m/yearto 10^–2 m/year, respectively, as the magmas evolved frombasaltic to andesitic compositions. Although the mechanism ofthe cooling (i.e. thermal convection and/or compositional convection)of the main magma could not be constrained uniquely by the model,it is suggested that compositional convection was not effectivein cooling the main magma, and the magma chamber is consideredto have been cooled by thermal convection, in addition to heatconduction. KEY WORDS: convection; magma chamber; heat and mass transport; timescale; U-series disequilibria     

Evolution of Holocene Dacite and Compositionally Zoned Magma, Volcan San Pedro, Southern Volcanic Zone, Chile

Volcán San Pedro in the Andean Southern Volcanic Zone(SVZ) Chile, comprises Holocene basaltic to dacitic lavas withtrace element and strontium isotope ratios more variable thanthose of most Pleistocene lavas of the underlying Tatara–SanPedro complex. Older Holocene activity built a composite coneof basaltic andesitic and silicic andesitic lavas with traceelement ratios distinct from those of younger lavas. Collapseof the ancestral volcano triggered the Younger Holocene eruptivephase including a sequence of lava flows zoned from high-K calc-alkalinehornblende–biotite dacite to two-pyroxene andesite. Notably,hornblende–phlogopite gabbroic xenoliths in the daciticlava have relatively low ⁸⁷Sr/⁸⁶Sr ratios identical to theirhost, whereas abundant quenched basaltic inclusions are moreradiogenic than any silicic lava. The latest volcanism rebuiltthe modern 3621 m high summit cone from basaltic andesite thatis also more radiogenic than the dacitic lavas. We propose thefollowing model for the zoned magma: (1) generation of hornblende–biotitedacite by dehydration partial melting of phlogopite-bearingrock similar to the gabbroic xenoliths; (2) forceful intrusionof basaltic magma into the dacite, producing quenched basalticinclusions and dispersion of olivine and plagioclase xenocryststhroughout the dacite; (3) cooling and crystallization–differentiationof the basalt to basaltic andesite; (4) mixing of the basalticandesite with dacite to form a small volume of two-pyroxenehybrid andesite. The modern volcano comprises basaltic andesitethat developed independently from the zoned magma reservoir.Evolution of dacitic and andesitic magma during the Holoceneand over the past 350 kyr reflects the intrusion of multiplemafic magmas that on occasion partially melted or assimilatedhydrous gabbro within the shallow crust. The chemical and isotopiczoning of Holocene magma at Volcán San Pedro is paralleledby that of historically erupted magma at neighboring VolcánQuizapu. Consequently, the role of young, unradiogenic hydrousgabbro in generating dacite and contaminating basalt may beunderappreciated in the SVZ. KEY WORDS: Andes; dacite; gabbro; Holocene; strontium isotopes     

Rates and Timescales of Fractional Crystallization from 238U-230Th-226Ra Disequilibria in Trachyte Lavas from Longonot Volcano, Kenya

A suite of peralkaline trachytes from Longonot volcano, Kenya,which erupted during the last 6000 years, has been analysedfor major and trace elements, Pb and Nd isotopes, and U–Th–Radisequilibria. The lavas are divided into three stratigraphicgroups of trachytes (Lt²a, Lt²b and Lt³), and hybrid lavas,designated LMx¹ and LMx², which, respectively, pre-date andpost-date the Lt² lavas. Major and trace elements are consistent,with up to 37% within-group fractional crystallization of predominantlyalkali feldspar. The parental magma for the different trachytegroups had a more mafic composition—probably hawaiitic.Nd and Pb isotopes show minimal variation, both within and betweenmagma groups, and indicate that up to 10% comendite magma fromthe neighbouring Olkaria volcanic field may have intermixedwith the Longonot magma. (²³⁰Th/²³⁸U) disequilibria indicatethat limited U/Th fractionation occurred during the past 10kyr, whereas (²²⁶Ra/²³⁰Th) disequilibria reflect the effectof alkali feldspar fractionation >8 kyr ago in the Lt²a lavas,between 3 and 7 kyr ago in the Lt²b lavas and in the past 3kyr for the Lt³ lavas. (²²⁶Ra/²³⁰Th) disequilibria in the Lt²blavas are interpreted using a model that combines the equationsof radioactive decay and in-growth with Rayleigh crystallizationto give fractionation rates of about 0·2 x 10^–4/yearfor the evolution of hawaiite to trachyte, but more rapid ratesof up to 3 x 10^–4/year for fractionation within the trachytesequence. (²²⁶Ra/²³⁰Th) from two whole-rock–alkali feldsparpairs are interpreted to show the crystals formed at 5800 yearsBP (Lt²b) and 2800 years BP (Lt³), implying that phenocrystformation continued almost up to the time of eruption. The resultsstrongly indicate that fractionated magmas can be stored forperiods on the order of 1000–2500 years prior to eruption,whereas other magmas were erupted as fractionation was proceeding. KEY WORDS: trachyte; magma chambers; u-series; Kenya     

Geochemistry of the Active Azufre--Planchon--Peteroa Volcanic Complex, Chile (3515'S): Evidence for Multiple Sources and Processes in a Cordilleran Arc Magmatic System

Along strike of the Quaternary magmatic arc in the SouthernVolcanic Zone of the Andes, there is a south to north increasein crustal thickness, and the lavas define systematic geochemicaltrends which have been attributed to variations in the proportionsand compositions of mantle-and crustal-derived components. Realisticinterpretations of these regional geochemical trends requiresan understanding of the sources and processes that control lavacompositions at individual volcanoes. Because it is in an importantgeophysical and geochemical transition zone, we studied theAzufre—Planchon—Peteroa volcanic complex, a nestedgroup of three volcanoes <055 m.y. in age located at 3515'Sin the Southern Volcanic Zone of the Andes. North of this complexat 33–35S the continental crust is thick, basalts areabsent, and there is abundant evidence for crustal componentsin the evolved lavas, but south of 37S, where the crust isrelatively thin, basaltic lavas are abundant and the contributionof continental crust to the lavas is less obvious. In additionto its location, this volcanic complex is important becausethere is a diversity of lava compositions, and it is the northernmostexposure of recent basaltic volcanism on the volcanic front.Therefore, the lavas of this complex can be used to identifythe relative roles of mantle, lower-crustal and upper-crustalsources and processes at a single location. Volcan Azufre is the oldest and largest volcano of the complex;it is a multi-cycle, bimodal, basaltic andesite–dacitestratovolcano. Volcan Planchon is the northernmost basalt-bearingvolcano along the volcanic front of the Southern Andes, andVolcan Peteroa, the youngest volcano of the complex, has eruptedmixed magmas of andesitic and dacitic composition. Most basalticandesite lavas at Azufre and Planchon are related by a plagioclase-poor,anhydrous mineral fractionating assemblage. High-alumina basaltis produced from a tholeiitic parent by an 4–8 kbar fractionatingassemblage. During this moderatepressure crystallization, themagmas also incorporated a crustal component with high La/Yband high abundances of Rb, Cs and Th. Based on the chemicalcharacteristics of the added component and the inferred depthof crystallization, the crustal source may have been garnetgranulite derived from solidified arc magmas in the lower tomiddle continental crust. At Planchon, the role of crustal assimilationhas increased with decreasing eruption age probably becausecrustal temperatures have increased during continued volcanism.Azufre dacite lavas formed at low pressures by fractionationof a plagioclase-rich assemblage. These dacite lavas containan upper-crustal component, probably derived in part from limestone,with high values of ⁸⁷Sr/⁸⁶Sr and ¹⁸O/¹⁶O. Thus two depths (upperand lower crust) of crystallization and associated crustal assimilationare evident in Planchon–Azufre lavas. Peteroa, the focusof recent volcanism, consists of calc-alkaline andesite anddacite eruptive products whose textures and compositions indicatean important role for magma mixing. Therefore, the volcanismevolved from a tholeiitic system of basalt and subordinate dacite(Planchon–Azufre) to a calc-alkaline system with abundantmixed lavas of intermediate composition (Peteroa). In additionto crustal thickness, two important parameters which controlledthe diversity of lava composition in this complex are magmasupply rate from the mantle and crustal temperature. Both parametersvaried with time, and they must be considered in broader interpretationsof along-strike geochemical trends. KEY WORDS: arc magmas; Andes; Peteroa; Planchan; geochemistry ^*Corresponding author. Present address: ENTRIX, Inc., 4II North Central Avenue, Glendale, CA 91203, USA     

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     

Crustal Evolution of Island-Arc Ultramafic Magma: Galmoenan Pyroxenite-Dunite Plutonic Complex, Koryak Highland (Far East Russia)

Alaskan-type platinum-bearing plutons and potassium-enrichedmafic to ultramafic volcanic rocks are temporally and spatiallyassociated within the Late Cretaceous–Paleocene Achaivayam–Valaginskiiintra-oceanic palaeo-arc system, allochthonously present inthe Koryak Highland and Kamchatka Peninsula (Far East Russia).The compositions of the parental magmas to the Alaskan-typecomplexes are estimated using the Galmoenan plutonic complexas an example. This complex, composed of dunites, pyroxenitesand minor gabbros, is the largest (20 km³) in the system andthe best studied owing to associated platinum placer deposits.The compositions of the principal mineral phases in the Galmoenanintrusive rocks [olivine (Fo_79–92), clinopyroxene (1–3·5wt % Al₂O₃, 0·1–0·5 wt % TiO₂), and Cr-spinel(5–15 wt % Al₂O₃ and 0·3–0·7 wt %TiO₂)] are typical of liquidus assemblages in primitive island-arcmagmas in intra-oceanic settings, and closely resemble the mineralcompositions in the Achaivayam–Valaginskii ultramaficvolcanic rocks. The temporal and spatial association of intrusiveand extrusive units, and the similarity of their mineral compositions,suggest that both suites were formed from similar parental magmas.The composition of the parental magma for the Galmoenan plutonicrocks is estimated using previously reported data for the Achaivayam–Valaginskiiultramafic volcanic rocks and phenocryst-hosted melt inclusions.Quantitative simulation of crystallization of the parental magmain the Galmoenan magma chamber shows that the compositions ofthe cumulate units are best modelled by fractional crystallizationwith periodic magma replenishment. The model calculations reproducewell the observed mineral assemblages and the trace elementabundances in clinopyroxene. Based upon the estimated compositionof the parental magmas and their mantle source, we considerthat fluxing of a highly refractory mantle wedge (similar tothe source of boninites) by chlorine-rich aqueous fluids isprimarily responsible for both high degrees of partial meltingand the geochemical characteristics of the magmas, includingtheir enrichment in platinum-group elements. KEY WORDS: subduction; platinum-group elements; clinopyroxene; trace elements; fractional crystallization; Alaskan-type plutons     

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.     

Magmatic Evolution of the La Pacana Caldera System, Central Andes, Chile: Compositional Variation of Two Cogenetic, Large-Volume Felsic Ignimbrites

La Pacana is one of the largest known calderas on Earth, andis the source of at least two major ignimbrite eruptions witha combined volume of some 2700 km³. These ignimbrites have stronglycontrasting compositions, raising the question of whether theyare genetically related. The Toconao ignimbrite is crystal poor,and contains rhyolitic (76–77 wt % SiO₂) tube pumices.The overlying Atana ignimbrite is a homogeneous tuff whose pumiceis dacitic (66–70 wt % SiO₂), dense (40–60% vesicularity)and crystal rich (30–40 % crystals). Phase equilibriaindicate that the Atana magma equilibrated at temperatures of770–790°C with melt water contents of 3·1–4·4wt %. The pre-eruptive Toconao magma was cooler (730–750°C)and its melt more water rich (6·3–6·8 wt% H₂O). A pressure of 200 MPa is inferred from mineral barometryfor the Atana magma chamber. Isotope compositions are variablebut overlapping for both units (⁸⁷Sr/⁸⁶Sr_i 0·7094–0·7131;¹⁴³Nd/¹⁴⁴Nd 0·51222–0·51230) and are consistentwith a dominantly crustal origin. Glass analyses from Atanapumices are similar in composition to those in Toconao tubepumices, demonstrating that the Toconao magma could representa differentiated melt of the Atana magma. Fractional crystallizationmodelling suggests that the Toconao magma can be produced by30% crystallization of the observed Atana mineral phases. Toconaomelt characteristics and intensive parameters are consistentwith a volatile oversaturation-driven eruption. However, thelow H₂O content, high viscosity and high crystal content ofthe Atana magma imply an external eruption trigger. KEY WORDS: Central Andes; crystal-rich dacite; eruption trigger; high-silica rhyolite; zoned magma chamber     

Mantle Preconditioning by Melt Extraction during Flow: Theory and Petrogenetic Implications

Mantle preconditioning may be defined as the extraction of smallmelt fractions from mantle asthenosphere during its flow tothe site of magma generation. Equations may be written for mantlepreconditioning, assuming that the mantle comprises enriched‘plums’ in a depleted matrix. The equations takeinto account variations in mass fraction of plums, the relativerate of melting of plums and matrix, the temperature and pressureof melt extraction, the mass fraction of melt extracted, theextent of chemical exchange between plums and matrix, and theefficiency of melt extraction. Monitoring mineralogical changesand variations in partition coefficients along the inferredP–T–t path of the mantle asthenosphere allows theequations to be correctly applied to the conditions under whichmelt extraction takes place. Numerical experiments demonstratethe influence of petrogenetic variables on the shape of meltextraction trajectories and provide new criteria for distinguishingbetween melt extraction and mixing as the cause of regionalgeochemical gradients. Representative examples of arc–back-arcsystems (Scotia), continental break-up (Afar) and plume–ridgeinteraction (Azores) indicate that the compositions of the mantlesources of mid-ocean ridge basalts and island arc basalts maybe determined, at least in part, by the melt extraction historiesof their asthenospheric sources. KEY WORDS: geochemical modelling; mantle flow; isotope ratios; trace elements     

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     

Melting of Amphibole-bearing Wehrlites: an Experimental Study on the Origin of Ultra-calcic Nepheline-normative Melts

Olivine + clinopyroxene ± amphibole cumulates have beenwidely documented in island arc settings and may constitutea significant portion of the lowermost arc crust. Because ofthe low melting temperature of amphibole (1100°C), suchcumulates could melt during intrusion of primary mantle magmas.We have experimentally (piston-cylinder, 0·5–1·0GPa, 1200–1350°C, Pt–graphite capsules) investigatedthe melting behaviour of a model amphibole–olivine–clinopyroxenerock, to assess the possible role of such cumulates in islandarc magma genesis. Initial melts are controlled by pargasiticamphibole breakdown, are strongly nepheline-normative and areAl₂O₃-rich. With increasing melt fraction (T > 1190°Cat 1·0 GPa), the melts become ultra-calcic while remainingstrongly nepheline-normative, and are saturated with olivineand clinopyroxene. The experimental melts have strong compositionalsimilarities to natural nepheline-normative ultra-calcic meltinclusions and lavas exclusively found in arc settings. Theexperimentally derived phase relations show that such naturalmelt compositions originate by melting according to the reactionamphibole + clinopyroxene = melt + olivine in the arc crust.Pargasitic amphibole is the key phase in this process, as itlowers melting temperatures and imposes the nepheline-normativesignature. Ultra-calcic nepheline-normative melt inclusionsare tracers of magma–rock interaction (assimilative recycling)in the arc crust. KEY WORDS: experimental melting; subduction zone; ultra-calcic melts; wehrlite     

Petrogenesis of the Largest Intraplate Volcanic Field on the Arabian Plate (Jordan): a Mixed Lithosphere-Asthenosphere Source Activated by Lithospheric Extension

Miocene to Recent volcanism in northwestern Arabia producedthe largest intraplate volcanic field on the Arabian plate (HarratAsh Shaam, Jordan). The chemically and isotopically diversevolcanic field comprises mafic alkali basalts and basanites.The magmas underwent limited fractional crystallization of ol± cpx ± plag and rare samples have assimilatedup to 20% of Late Proterozoic crust en route to the surface.However, there are subtle Sr–Nd–Pb isotopic variations(⁸⁷Sr/⁸⁶Sr = 0·70305–0·70377, ¹⁴³Nd/¹⁴⁴Nd= 0·51297–0·51285, ²⁰⁶Pb/²⁰⁴Pb = 18·8–19·2),which exhibit marked correlations with major elements, incompatibletrace element ratios and abundances in relatively primitivebasalts (MgO >8·5 wt %), and cannot be explained byfractional crystallization and crustal contamination alone.Instead, the data require polybaric melting of heterogeneoussources. Semi-quantitative melt modelling suggests that thisheterogeneity is the result of small degree melts (2–5%)from spinel- and garnet-facies mantle, inferred to be shallowArabian lithosphere, that mixed with smaller degree melts (<1%)from a predominantly deep garnet-bearing asthenospheric(?) sourcewith ocean island basalt characteristics. The latter may bea ubiquitous part of the asthenosphere but is preferentiallytapped at small degrees of partial melting. Volcanism in Jordanappears to be the result of melting lithospheric mantle in responseto lithospheric extension. With time, thinning of the lithosphereallowed progressively deeper mantle (asthenosphere?) to be activatedand melts from this to mix with the shallower lithospheric mantlemelts. Although Jordanian intraplate volcanism is isotopicallysimilar to examples of Late Cenozoic volcanism throughout theArabian peninsula (Israel, Saudi Arabia), subtle chemical andisotopic differences between Yemen and Jordan intraplate volcanismsuggest that the Afar plume has not been channelled northwestwardsbeneath the Arabian plate and played no role in producing thenorthern Saudi Arabian and Jordan intraplate volcanic fields. KEY WORDS: asthenosphere; intraplate volcanism; Jordan; lithospheric mantle; Sr–Nd–Pb isotopes     

Petrology and Geochemistry of the Bandas del Sur Formation, Las Canadas Edifice, Tenerife (Canary Islands)

The Bandas del Sur Formation preserves a Quaternary extra-calderarecord of central phonolitic explosive volcanism of the LasCañadas volcano at Tenerife. Volcanic rocks are bimodalin composition, being predominantly phonolitic pyroclastic deposits,several eruptions of which resulted in summit caldera collapse,alkali basaltic lavas erupted from many fissures around theflanks. For the pyroclastic deposits, there is a broad rangeof pumice glass compositions from phonotephrite to phonolite.The phonolite pyroclastic deposits are also characterized bya diverse, 7–8-phase phenocryst assemblage (alkali feldspar+ biotite + sodian diopside + titanomagnetite + ilmenite + nosean–haüyne+ titanite + apatite) with alkali feldspar dominant, in contrastto interbedded phonolite lavas that typically have lower phenocrystcontents and lack hydrous phases. Petrological and geochemicaldata are consistent with fractional crystallization (involvingthe observed phenocryst assemblages) as the dominant processin the development of phonolite magmas. New stratigraphicallyconstrained data indicate that petrological and geochemicaldifferences exist between pyroclastic deposits of the last twoexplosive cycles of phonolitic volcanism. Cycle 2 (0·85–0·57Ma) pyroclastic fall deposits commonly show a cryptic compositionalzonation indicating that several eruptions tapped chemically,and probably thermally stratified magma systems. Evidence formagma mixing is most widespread in the pyroclastic depositsof Cycle 3 (0·37–0·17 Ma), which includesthe presence of reversely and normally zoned phenocrysts, quenchedmafic glass blebs in pumice, banded pumice, and bimodal to polymodalphenocryst compositional populations. Syn-eruptive mixing eventsinvolved mostly phonolite and tephriphonolite magmas, whereasa pre-eruptive mixing event involving basaltic magma is recordedin several banded pumice-bearing ignimbrites of Cycle 3. Theperiodic addition and mixing of basaltic magma ultimately mayhave triggered several eruptions. Recharge and underplatingby basaltic magma is interpreted to have elevated sulphur contents(occurring as an exsolved gas phase) in the capping phonoliticmagma reservoir. This promoted nosean–haüyne crystallizationover nepheline, elevated SO₃ contents in apatite, and possiblyresulted in large, climatologically important SO₂ emissions. KEY WORDS: Tenerife; phonolite; crystal fractionation; magma mixing; sulphur-rich explosive eruptions     

A Complex Petrogenesis for an Arc Magmatic Suite, St Kitts, Lesser Antilles

St Kitts forms one of the northern group of volcanic islandsin the Lesser Antilles arc. Eruptive products from the Mt Liamuigacentre are predominantly olivine + hypersthene-normative, low-Kbasalts through basaltic andesites to quartz-normative, low-Kandesites. Higher-Al and lower-Al groups can be distinguishedin the suite. Mineral assemblages include olivine, clinopyroxene,orthopyroxene, plagioclase and titanomagnetite with rarer amphibole,ilmenite and apatite. Eruptive temperatures of the andesitesare estimated as 963–950°C at fO₂ NNO + 1 (whereNNO is the nickel–nickel oxide buffer). Field and mineralchemical data provide evidence for magma mixing. Glass (melt)inclusions in the phenocrysts range in composition from andesiteto high-silica rhyolite. Compositional variations are broadlyconsistent with the evolution of more evolved magmas by crystalfractionation of basaltic parental magmas. The absence of anycovariation between ⁸⁷Sr/⁸⁶Sr or ¹⁴³Nd/¹⁴⁴Nd and SiO₂ rulesout assimilation of older silicic crust. However, positive correlationsbetween Ba/La, La/Sm and ²⁰⁸Pb/²⁰⁴Pb and between ²⁰⁸Pb/²⁰⁴Pband SiO₂ are consistent with assimilation of small amounts (<10%)of biogenic sediments. Trace element and Sr–Nd–Pbisotope data suggest derivation from a normal mid-ocean ridgebasalt (N-MORB)-type mantle source metasomatized by subductedsediment or sediment melt and fluid. The eruptive rocks arecharacterized by ²³⁸U excesses that indicate that fluid additionof U occurred <350 kyr ago; U–Th isotope data for mineralseparates are dominated by melt inclusions but would allow crystallizationages of 13–68 ka. However, plagioclase is consistentlydisplaced above these ‘isochrons’, with apparentages of 39–236 ka, and plagioclase crystal size distributionsare concave-upwards. These observations suggest that mixingprocesses are important. The presence of ²²⁶Ra excesses in twosamples indicates some fluid addition <8 kyr ago and thatthe magma residence times must also have been less than 8 kyr. KEY WORDS: Sr–Nd–Pb isotopes; U-series isotopes; crystal size distribution; petrogenesis     

Petrogenesis of Mafic Inclusions in Rhyolitic Lavas from Narugo Volcano, Northeastern Japan

Mafic inclusions present in the rhyolitic lavas of Narugo volcano,Japan, are vesiculated andesites with diktytaxitic texturesmainly composed of quenched acicular plagioclase, pyroxenes,and interstitial glass. When the mafic magma was incorporatedinto the silica-rich host magma, the cores of pyroxenes andplagioclase began to crystallize (>1000°C) in a boundarylayer between the mafic and felsic magmas. Phenocryst rim compositionsand interstitial glass compositions (average 78 wt % SiO₂) inthe mafic inclusions are the same as those of the phenocrystsand groundmass glass in the host rhyolite. This suggests thatthe host felsic melt infiltrated into the incompletely solidifiedmafic inclusion, and that the interstitial melt compositionin the inclusions became close to that of the host melt (c.850°C). Infiltration was enhanced by the vesiculation ofthe mafic magma. Finally, hybridized and density-reduced portionsof the mafic magma floated up from the boundary layer into thehost rhyolite. We conclude that the ascent of mafic magma triggeredthe eruption of the host rhyolitic magma. KEY WORDS: mafic inclusion; stratified magma chamber; magma mixing; mingling; Narugo volcano; Japan     

Timescales of magma differentiation from basalt to andesite beneath Hekla Volcano, Iceland: Constraints from U-series disequilibria in lavas from the last quarter-millennium flows

Measurements of ²³⁸U-²³⁰Th-²²⁶Ra disequilibria, Sr-Nd-Pb-Hf isotopes and major-trace elements have been conducted for lavas erupted in the last quarter-millennium at Hekla volcano, Iceland. The volcanic rocks range from basalt to dacite. Most of the lavas (excluding dacitic samples) display limited compositional variations in radiogenic Sr-Nd-Pb-Hf isotopes (⁸⁷Sr/⁸⁶Sr = 0.70319-0.70322; ¹⁴³Nd/¹⁴⁴Nd = 0.51302-0.51305; ²⁰⁶Pb/²⁰⁴Pb = 19.04-19.06; ²⁰⁷Pb/²⁰⁴Pb = 15.53-15.54; ²⁰⁸Pb/²⁰⁴Pb = 38.61-38.65; ¹⁷⁶Hf/¹⁷⁷Hf = 0.28311-0.28312). All the samples possess (²³⁰Th/²³⁸U) disequilibrium with ²³⁰Th excesses, and they show systematic variations in (²³⁰Th/²³²Th) and (²³⁸U/²³²Th) ratios. The highest ²²⁶Ra excesses occur in the basalt and most differentiated andesite lavas, while some basaltic-andesite lavas have (²²⁶Ra/²³⁰Th) ratio that are close to equilibrium. The ²³⁸U-²³⁰Th-²²⁶Ra disequilibria variations cannot be produced by simple closed-system fractional crystallization with radioactive decay of ²³⁰Th and ²²⁶Ra in a magma chamber. A closed-system fractional crystallization model and assimilation and fractional crystallization (AFC) model indicate that the least differentiated basaltic andesites were derived from basalt by fractional crystallization with a differentiation age of ∼24 ± 11 kyr, whereas the andesites were formed by assimilation of crustal material and fractionation of the basaltic-andesites within 2 kyr. Apatite is inferred to play a key role in fractionating the parent-daughter nuclides in ²³⁰Th-²³⁸U and ²²⁶Ra-²³⁰Th to make the observed variations. Our proposed model is that several batches of basaltic-andesite magmas that formed by fractional crystallization of a basaltic melt from a deeper reservoir, were periodically injected into the shallow crust to form individual magma pockets, and subsequently modifying the original magma compositions via simultaneous assimilation and fractional crystallization. The assimilant is the dacitic melt, which formed by partial melting of the crust.