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     

Magmatic processes and mixing origin of andesite: Miocene Karamağara volcanics,Central Anatolia,Turkey

The Miocene Karamağara volcanics (KMV) crop out in the Saraykent region (Yozgat) of Central Anatolia. The KMV include four principal magmatic components based on their petrography and compositional features: basaltic andesites (KMB); enclaves (KME); andesites (KMA); and dacites (KMD). Rounded and ellipsoidal enclaves occur in the andesites, ranging in diameter from a few millimetres to ten centimetres. A non‐cognate origin for the enclaves is suggested due to their mineralogical dissimilarity to the enclosing andesites. The enclaves range in composition from basaltic andesite to andesite. Major and trace element data and primitive mantle‐normalized rare‐earth element (REE) patterns of the KMV exhibit the effects of fractional crystallization on the evolution of the KME which are the product of mantle‐derived magma. The KMA contain a wide variety of phenocrysts, including plagioclase, clinopyroxene, orthopyroxene, hornblende and opaque minerals. Comparison of textures indicates that many of the hornblende phenocrysts within the KMA were derived from basaltic andesites (KMB) and are not primary crystallization products of the KMA. Evidence of disequilibrium in the hybrid andesite includes the presence of reacted hornblendes, clinopyroxene mantled by orthopyroxene and vice versa, and sieve‐texture and inclusion zones within plagioclase. The KMV exhibit a complex history, including fractional crystallization, magma mixing and mingling processes between mantle and crust‐derived melts. Textural and geochemical characteristics of the enclaves and their hosts require that mantle‐derived basic magma intruded the deep continental crust followed by fractional crystallization and generation of silicic melts from the continental material. Hybridization between basic and silicic melts subsequently occurred in a shallow magma chamber. Modelling of major element geochemistry suggests that the hybrid andesite represents a 62:38 mix of dacite and basaltic andesite. The implication of this process is that calc‐alkaline intermediate volcanic rocks in the Saraykent region represent hybrids resulting from mixing between basic magma derived from the mantle and silicic magma derived from the continental crust. Copyright © 2005 John Wiley & Sons, Ltd.     

Fractional crystallization and mantle-melting controls on calc-alkaline differentiation trends

The phase relations of primitive magnesian andesites and basaltic andesites from the Mt. Shasta region, N California have been determined over a range of pressure and temperature conditions and H₂O contents. The experimental results are used to explore the influence of H₂O and pressure on fractional crystallization and mantle melting behavior in subduction zone environments. At 200-MPa H₂O-saturated conditions the experimentally determined liquid line of descent reproduces the compositional variation found in the Mt. Shasta region lavas. This calc-alkaline differentiation trend begins at the lowest values of FeO*/MgO and the highest SiO₂ contents found in any arc magma system and exhibits only a modest increase in FeO*/MgO with increasing SiO₂. We propose a two-stage process for the origin of these lavas. (1) Extensive hydrous mantle melting produces H₂O-rich (>4.5--6 wt% H₂O) melts that are in equilibrium with a refractory harzburgite (olivine + orthopyroxene) residue. Trace elements and H₂O are contributed from a slab-derived fluid and/or melt. (2) This mantle melt ascends into the overlying crust and undergoes fractional crystallization. Crustal-level differentiation occurs under near-H₂O saturated conditions producing the distinctive high SiO₂ and low FeO*/MgO characteristics of these calc-alkaline andesite and dacite lavas. In a subset of Mt. Shasta region lavas, magnesian pargasitic amphibole provides evidence of high pre-eruptive H₂O contents (>10 wt% H₂O) and lower crustal crystallization pressures (800 MPa). Igneous rocks that possess major and trace element characteristics similar to those of the Mt. Shasta region lavas are found at Adak, Aleutians, Setouchi Belt, Japan, the Mexican Volcanic Belt, Cook Island, Andes and in Archean trondhjemite--tonalite--granodiorite suites (TTG suites). We propose that these magmas also form by hydrous mantle melting.Editorial responsibility: J. Hoefs     

The Tatara-San Pedro Volcano, 36 S, Chile: A Chemically Variable, Dominantly Mafic Magmatic System

The Tatara shield volcano and subsequent San Pedro cone arethe youngest edifices of the San Pedro-Pellado volcanic complexat 36S in the Chilean Andes. There are multiple basaltic andesitecompositional types present in the Tatara volcano, which couldresult from either contrasting source regions or interactionof primitive liquids with heterogeneous crust. The eruptivestratigraphy of the magma types implies concurrent, isolatedmagma chambers beneath Tatara-San Pedro. Open-system processesand multiple crustal endmembers were involved in calcalkalinedifferentiation series, whereas a tholeitiic series evolvedmainly by fractional crystallization. The glaciated Tatara shield comprises two cycles of compositionallydiverse basaltic andesite lavas, each of which is capped byvolumetrically minor andesite to dacite lavas. Four types (I-IV)of basaltic andesite are defined on the basis of chemical criteria,two in each cycle. The early cycle consists of calcalkalinetype I basaltic andesites, and tholeiitic type II basaltic andesitesand andesites; it culminated in the eruption of a dacite dome.The later cycle comprises intercalated calcalkaline type IIIand IV basaltic andesites, and they are overlain by San Pedroandesites and dacites which appear to be the differentiationproducts of type IV magmas. Tatara lavas were erupted from acommon vent situated beneath the modern San Pedro cone. Althoughthey overlap temporally and spatially, there is little evidenceof chemical interaction among the different lava types, indicatingthat there were two or more magma reservoirs beneath Tatara-SanPedro. Chemical differences among the basaltic andesite types precludederivation of any one from any of the others by fractional crystallization,assimilation-fractional crystallization (AFC), or magma mixing.The differences seem to reflect chemically different parentmagmas. The type I and IV parent liquids were relatively highin MgO, low in CaO and AI₂O₃, and had high incompatible andcompatible element abundances. The type II and III parents werelower in MgO, higher in A1₂O₃ and CaO, and had lower compatibleand incompatible element abundances. Tholeiitic type II lavasappear to have evolved mainly by fractional crystallization,whereas there is evidence of open-system processes such as AFCand magma mixing in the evolution of the calcalkaline I, III,and IV suites. The chemical evolution of the type III and type IV-San Pedromagma suites has been simulated by assimilation and mixing modelsusing local granites and xenoliths as assimilants. The xenolithsprobably represent portions of a sub-caldera pluton associatedwith the Quebrada Turbia Tuff, which erupted from the Rio Coloradocaldera within the San Pedro-Pellado complex at 0–487Ma. Chemical and textural variations in type III lavas correlatewith stratigraphic position and appear to represent mixing betweena parental type III magma and remnant, evolved type I magmathat was progressively flushed from its chamber concurrent withmixing. The youngest San Pedro flow is chemically zoned fromdacite to basaltic andesite and may have formed by mixing withina conduit during eruption.     

Petrological and experimental evidence for differentiation of water-rich magmas beneath St. Kitts,Lesser Antilles

St. Kitts lies in the northern Lesser Antilles, a subduction-related intraoceanic volcanic arc known for its magmatic diversity and unusually abundant cognate xenoliths. We combine the geochemistry of xenoliths, melt inclusions and lavas with high pressure–temperature experiments to explore magma differentiation processes beneath St. Kitts. Lavas range from basalt to rhyolite, with predominant andesites and basaltic andesites. Xenoliths, dominated by calcic plagioclase and amphibole, typically in reaction relationship with pyroxenes and olivine, can be divided into plutonic and cumulate varieties based on mineral textures and compositions. Cumulate varieties, formed primarily by the accumulation of liquidus phases, comprise ensembles that represent instantaneous solid compositions from one or more magma batches; plutonic varieties have mineralogy and textures consistent with protracted solidification of magmatic mush. Mineral chemistry in lavas and xenoliths is subtly different. For example, plagioclase with unusually high anorthite content (An_≤100) occurs in some plutonic xenoliths, whereas the most calcic plagioclase in cumulate xenoliths and lavas are An₉₇ and An₉₅, respectively. Fluid-saturated, equilibrium crystallisation experiments were performed on a St. Kitts basaltic andesite, with three different fluid compositions (XH₂O = 1.0, 0.66 and 0.33) at 2.4 kbar, 950–1025 °C, and fO₂ = NNO ? 0.6 to NNO + 1.2 log units. Experiments reproduce lava liquid lines of descent and many xenolith assemblages, but fail to match xenolith and lava phenocryst mineral compositions, notably the very An-rich plagioclase. The strong positive correlation between experimentally determined plagioclase-melt Kd_Ca–Na and dissolved H₂O in the melt, together with the occurrence of Al-rich mafic lavas, suggests that parental magmas were water-rich (> 9 wt% H₂O) basaltic andesites that crystallised over a wide pressure range (1.5–6 kbar). Comparison of experimental and natural (lava, xenolith) mafic mineral composition reveals that whereas olivine in lavas is predominantly primocrysts precipitated at low-pressure, pyroxenes and spinel are predominantly xenocrysts formed by disaggregation of plutonic mushes. Overall, St. Kitts xenoliths and lavas testify to mid-crustal differentiation of low-MgO basalt and basaltic andesite magmas within a trans-crustal, magmatic mush system. Lower crustal ultramafic cumulates that relate parental low-MgO basalts to primary, mantle -derived melts are absent on St. Kitts.     

Magnesian andesite and dacite lavas from Mt. Shasta,northern California: products of fractional crystallization of H<Subscript>2</Subscript>O-rich mantle melts

Mt. Shasta andesite and dacite lavas contain high MgO (3.5–5 wt.%), very low FeO*/MgO (1–1.5) and 60–66 wt.% SiO₂. The range of major and trace element compositions of the Shasta lavas can be explained through fractional crystallization (~50–60 wt.%) with subsequent magma mixing of a parent magma that had the major element composition of an H₂O-rich primitive magnesian andesite (PMA). Isotopic and trace element characteristics of the Mt. Shasta stratocone lavas are highly variable and span the same range of compositions that is found in the parental basaltic andesite and PMA lavas. This variability is inherited from compositional variations in the input contributed from melting of mantle wedge peridotite that was fluxed by a slab-derived, fluid-rich component. Evidence preserved in phenocryst assemblages indicates mixing of magmas that experienced variable amounts of fractional crystallization over a range of crustal depths from ~25 to ~4 km beneath Mt. Shasta. Major and trace element evidence is also consistent with magma mixing. Pre-eruptive crystallization extended from shallow crustal levels under degassed conditions (~4 wt.% H₂O) to lower crustal depths with magmatic H₂O contents of ~10–15 wt.%. Oxygen fugacity varied over 2 log units from one above to one below the Nickel-Nickel Oxide buffer. The input of buoyant H₂O-rich magmas containing 10–15 wt.% H₂O may have triggered magma mixing and facilitated eruption. Alternatively, vesiculation of oversaturated H₂O-rich melts could also play an important role in mixing and eruption.     

Geochemistry of Neogene quartz andesites from the Oaş and Gutâi Mountains,Eastern Carpathians (Romania): a complex magma genesis

The Neogene quartz andesites from the Oa? and Gutâi Mountains (Romania) are mid-K calc-alkaline rocks and contain plagioclase-orthopyroxene-clinopyroxene-amphibole-magnetite phenocrysts as well as quartz crystals. They are associated with a volcanic sequence ranging from basalts and basaltic andesites to dacites and rhyolites, but form a separate magma group, mostly in respect to the trace elements. Based on the geochemical data combined with inferences from complex zoning patterns in plagioclase and pyroxene, the evolution of quartz andesites is interpreted in terms of fractional crystallization, AFC and magma mixing. A parental magma deriving from a MORB- or OIB-type source modified by fluids and melts originating from sediments is envisaged.     

Geology, petrochemistry, and genesis of the bimodal lavas of Osham Hill, Saurashtra, northwestern Deccan Traps

The Saurashtra region in the northwestern Deccan continental flood basalt province (India) is notable for compositionally diverse volcano-plutonic complexes and abundant rhyolites and granophyres. A lava flow sequence of rhyolite-pitchstone-basaltic andesite is exposed in Osham Hill in western Saurashtra. The Osham silicic lavas are Ba-poor and with intermediate Zr contents compared to other Deccan rhyolites. The Osham silicic lavas are enriched in the light rare earth elements, and have ε_Nd (t = 65 Ma) values between −3.1 and −6.5 and initial ⁸⁷Sr/⁸⁶Sr ratios of 0.70709-0.70927. The Osham basaltic andesites have initial ε_Nd values between +2.2 and −1.3, and initial ⁸⁷Sr/⁸⁶Sr ratios of 0.70729-0.70887. Large-ion-lithophile element concentrations and Sr isotopic ratios may have been affected somewhat by weathering; notably, the Sr isotopic ratios of the silicic and mafic rocks overlap. However, the Nd isotopic data indicate that the silicic lavas are significantly more contaminated by continental lithosphere than the mafic lavas. We suggest that the Osham basaltic andesites were derived by olivine gabbro fractionation from low-Ti picritic rocks of the type found throughout Saurashtra. The isotopic compositions, and the similar Al₂O₃ contents of the Osham silicic and mafic lavas, rule out an origin of the silicic lavas by fractional crystallization of mafic liquids, with or without crustal assimilation. As previously proposed for some Icelandic rhyolites, and supported here by MELTS modelling, the Osham silicic lavas may have been derived by partial melting of hot mafic intrusions emplaced at various crustal depths, due to heating by repetitively injected basalts. The absence of mixing or mingling between the rhyolitic and basaltic andesite lavas of Osham Hill suggests that they reached the surface via separate pathways.     

Crystal Accumulation and Magma Mixing in the Petrogenesis of Tholeiitic Andesites from Fukujin Seamount, Northern Mariana Island Arc

Fukujin Seamount is a large, active, submarine volcano on thevolcanic front in the northernseamount province (NSP) of theMariana island arc (MIA). Five dredge hauls from the summitand upper flanks of Fukujin recovered mainly highly porphyriticbasaltic andesites. A few nearly aphyric samples are medium-Ksiliceous andesites (SiO₂ = 62%, K₂O = 1•5%). Fukujin andmost other large arc-front volcanoes of the northern MIA havetholeiitic (iron-enrichment) fractionation trends. This contrastswith the calc-alkaline trends of many smaller seamounts. A negativecorrelation of modal plagioclase content with bulk-rock SiO₂,as well as bulk-rock major and trace element variation trends,and glass analyses, suggests that lavas with >30 vol.% phenocrystsand <55 wt.% SiO₂ are partial cumulates. The presence ofbimodal phenocryst populations along with reversed to normalzoning of phenocrysts is explained by magma mixing of andesiticand basaltic liquids. Hybrid basaltic andesites probably formedby the accumulation of plagioclase in a tholeiitic magma chamberundergoing replenishment and mixing at a shallow crustal level.A petrogenetic model is presented for the origin of basalticandesite by combined magma mixing and fractional crystallization.Aphyric siliceous andesites can be modelled by simple fractionationof basaltic andesite. The early fractionating assemblage consistedmainly of plagioclase and clinopyroxene, with lesser olivineand minor magnetite, but plagioclase remained suspended in themelt. The later fractionating assemblage was dominated by plagioclasewith orthopyroxene instead of olivine. ^*Present address: 2260 rue Panet, Montreal, Quebec, H2L 3A6, Canada.     

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.     

Temporal magmatic variation at Boqueron volcano,El Salvador

The relative ages of 21 lavas from Boqueron volcano in El Salvador were determined by superposition. The lavas are grey to black, porphyritic basalts, basaltic andesites and andesites with phenocrysts of plagioclase, augite, olivine, and magnetite. The andesitic lavas appear to have evolved from basaltic magma by fractionation of the observed phenocryst phases.The temporal variation in the chemical composition of the lavas at Boqueron is composed of three components. First, there is a crudely cyclical alternation of basalts and andesites. Second, these cycles are progressively shifted toward higher SiO₂ contents. Third, approximately in the middle of the stratigraphic section sampled, there is an abrupt change in chemical variation trends from an Al-rich and Fe-poor trend to an Fe-rich and Al-poor trend. This change is interpreted to have been caused by an increased proportion of plagioclase fractionation and a decreased porportion of augite fractionation. The crudely cyclical change in SiO₂ content with time is interpreted as a combination of crystal fractionation that increases SiO₂ content, followed by influxes of basaltic magma that mix with residual magma to decrease SiO₂ content. Successive cycles are shifted toward higher SiO₂ content because there is a significant volume of fractionated magma remaining in the chamber before each influx of basalt.     

Variations in andean andesite compositions and their petrogenetic significance

Three linear zones of active andesite volcanism are present in the Andes — a northern zone (5°N–2°S) in Colombia and Ecuador, a central zone (16°S–28°S) largely in south Peru and north Chile and a southern zone (33°S–52°S) largely in south Chile. The northern zone is characterized by basaltic andesites, the central zone by andesite—dacite lavas and ignimbrites and the southern zone by high-alumina basalts, basaltic andesites and andesites. Shoshonites and volcanic rocks of the alkali basalt—trachyte association occur at scattered localities east of the active volcanic chain,The northern and central volcanic zones are 140 km above an eastward-dipping Benioff zone, while the southern zone lies only 90 km above a Benioff zone. Continental crust is ca. 70 km in thickness below the central zone, but is 30–45 km thick below northern and southern volcanic zones. The correlation between volcanic products and their structural setting is supported by trace element and isotope data. The central zone andesite lavas have higher Si, K, Rb, Sr and Ba, and higher initial Sr isotope ratios than the northern or southern zone lavas. The southern zone high-alumina basalts have lower Ce/Yb ratios than volcanics from the other zones. In addition, the central zone andesite lavas show a well-defined eastward increase in K, Rb and Ba and a decrease in Sr.Andean andesite magmas are a result of a complex interplay of partial melting, fractional crystallization and “contamination” processes at mantle depths, and contamination and fractional crystallization in the crust. Variations in andesite composition across the central Andean chain reflect a diminishing degree of partial melting or an increase in fractional crystallization or an increase in “contamination” passing eastwards. Variations along the Andean chain indicate a significant crustal contribution for andesites in the central zone, and indicate that the high-alumina basalts and basaltic andesites of the southern zone are from a shallower mantle source region than other volcanic rocks. The dacite-rhyolite ignimbrites of the central zone share a common source with the andesites and might result from fractional crystallization of andesite magma during uprise through thick continental crust. The occurrence of shoshonites and alkali basalts eat of the active volcanic chain is attributed to partial melting of mantle peridotite distant from the subduction zone.     

Petrology and geochemistry of Camiguin Island, southern Philippines: insights to the source of adakites and other lavas in a complex arc setting

Camiguin is a small volcanic island located 12 km north of Mindanao Island in southern Philippines. The island consists of four volcanic centers which have erupted basaltic to rhyolitic calcalkaline lavas during the last ∼400 ka. Major element, trace element and Sr, Nd and Pb isotopic data indicate that the volcanic centers have produced a single lava series from a common mantle source. Modeling results indicate that Camiguin lavas were produced by periodic injection of a parental magma into shallow magma chambers allowing assimilation and fractional crystallization (AFC) processes to take place. The chemical and isotopic composition of Camiguin lavas bears strong resemblance to the majority of lavas from the central Mindanao volcanic field confirming that Camiguin is an extension of the tectonically complex Central Mindanao Arc (CMA). The most likely source of Camiguin and most CMA magmas is the mantle wedge metasomatized by fluids dehydrated from a subducted slab. Some Camiguin high-silica lavas are similar to high-silica lavas from Mindanao, which have been identified as “adakites” derived from direct melting of a subducted basaltic crust. More detailed comparison of Camiguin and Mindanao adakites with silicic slab-derived melts and magnesian andesites from the western Aleutians, southernmost Chile and Batan Island in northern Philippines indicates that the Mindanao adakites are not pure slab melts. Rather, the CMA adakites are similar to Camiguin high-silica lavas which are products of an AFC process and have negligible connection to melting of subducted basaltic crust. Received: 27 February 1998 / Accepted: 27 August 1998     

Assimilation and fractionation in adjacent parts of the same magme chamber: Vandfaldsdalen macrodike,East Greenland

The Vandfaldsdalen macrodike, which lies in the Skaergaard region of East Greenland, is a remarkably zoned fossil magma chamber, with a granophyric cap overlying cumulate gabboros. The intrusion is distinctly bimodal, with a large compositional discontinuity at the contact between the gabbro and granophyre. Although the exposed part of the macrodike is in contact with Tertiary basalts and sediments, the granophyre originated by assimilation of xenoliths derived from the underlying Archean basement. Sr and Nd isotopic ratios throughout the cumulate sequence are remarkably similar, indicating insignificant contamination of the gabbro by the granophyre. Modelling of the compositional effects of cooling and crystallization indicate that the cumulate pile resulted from fractional crystallization, with the complicating effects of trapped liquid and post-cumulus fractionation. The uppermost rocks in the mafic part, of the chamber (SiO₂=62%; FeO^*=12.4%) resulted from about 85% fractional crystallization. A transgressive sill of strongly fractionated magma (SiO₂=67%; FeO^*=8.8%) formed from extracted intercumulus liquid that was the result of 90% fractional crystallization of the original magma. Mass-balance indicates that typical granophyre is made up of about 75% dissolved xenoliths, by weight, and 25% mantle-derived basaltic magma. The magmas were not measurably affected by material exchange across the interface between the gabbro and granophyre. This magma chamber evolved by both assimilation and fractional crystallization, but the residual liquids formed by fractional crystallization were unaffected by assimilation. Heat exchange between were unaffected by assimilation. Heat exchange between the two parts of the chamber was obviously important, but there was insignificant material exchange. The inability of fractional crystallization and assimilation to affect the same liquid is related to the dynamic behavior of this particular magma chamber, particularly the buoyancy of granophyre relative to evolving tholeiitic magma.     

Origin of calc-alkaline series lavas at Medicine Lake Volcano by fractionation,assimilation and mixing

The results of experimental studies and examination of variations in major elements, trace elements and Sr isotopes indicate that fractionation, assimilation and magma mixing combined to produce the lavas at Medicine Lake Highland. Some characteristics of the compositional differences among the members of the calc-alkalic association (basalt-andesite-dacite-rhyolite) can be produced by fractional crystallization, and a fractionation model reproduces the major element trends. Other variations are inconsistent with a fractionation origin. Elevated incompatible element abundances (K and Rb) observed in lavas intermediate between basalt and rhyolite can be produced through assimilation of a crustal component. An accompanying increase in ⁸⁷Sr/⁸⁶Sr from ∼ 0.07030 in basalt to ∼0.7040 in rhyolite is also consistent with crustal assimilation. The compatible trace element contents (Ni and Sr) of intermediate lavas can not be produced by fractional crystallization, and suggest a magma-mixing origin for some lavas. Unusual phenocryst assemblages and textural criteria in these lavas provide additional evidence for magma mixing. A phase diagram constructed from the low pressure melting experiments identifies a distributary reaction point, where olivine+augite react to pigeonite. Parental basalts reach this point at low pressures and undergo iron-enrichment at constant SiO₂ content. The resulting liquid line of descent is characteristic of the tholeiitic trend. Calc-alkalic differentiation trends circumvent the distributary reaction point by three processes: fractionation at elevated pH₂O, assimilation and magma mixing.     

Fluid history of UHP metamorphism in Dabie Shan, China: a fluid inclusion and oxygen isotope study on the coesite-bearing eclogite from Bixiling

This paper characterizes late Holocene basalts and basaltic andesites at Medicine Lake volcano that contain high pre-eruptive H₂O contents inherited from a subduction related hydrous component in the mantle. The basaltic andesite of Paint Pot Crater and the compositionally zoned basaltic to andesitic lavas of the Callahan flow erupted approximately 1000 ¹⁴C years Before Present (¹⁴C years b.p.). Petrologic, geochemical and isotopic evidence indicates that this late Holocene mafic magmatism was characterized by H₂O contents of 3 to 6 wt% H₂O and elevated abundances of large ion lithophile elements (LILE). These hydrous mafic inputs contrast with the preceding episodes of mafic magmatism (from 10,600 to ∼3000 ¹⁴C years b.p.) that was characterized by the eruption of primitive high alumina olivine tholeiite (HAOT) with low H₂O (<0.2 wt%), lower LILE abundance and different isotopic characteristics. Thus, the mantle-derived inputs into the Medicine Lake system have not always been low H₂O, primitive HAOT, but have alternated between HAOT and hydrous subduction related, calc-alkaline basalt. This influx of hydrous mafic magma coincides temporally and spatially with rhyolite eruption at Glass Mountain and Little Glass Mountain. The rhyolites contain quenched magmatic inclusions similar in character to the mafic lavas at Callahan and Paint Pot Crater. The influence of H₂O on fractional crystallization of hydrous mafic magma and melting of pre-existing granite crust beneath the volcano combined to produce the rhyolite. Fractionation under hydrous conditions at upper crustal pressures leads to the early crystallization of Fe-Mg silicates and the suppression of plagioclase as an early crystallizing phase. In addition, H₂O lowers the saturation temperature of Fe and Mg silicates, and brings the temperature of oxide crystallization closer to the liquidus. These combined effects generate SiO₂-enrichment that leads to rhyodacitic differentiated lavas. In contrast, low H₂O HAOT magmas at Medicine Lake differentiate to iron-rich basaltic liquids. When these Fe-enriched basalts mix with melted granitic crust, the result is an andesitic magma. Since mid-Holocene time, mafic volcanism has been dominated primarily by hydrous basaltic andesite and andesite at Medicine Lake Volcano. However, during the late Holocene, H₂O-poor mafic magmas continued to be erupted along with hydrous mafic magmas, although in significantly smaller volumes. Received: 4 January 1999 / Accepted: 30 August 1999     

Petrographic and Geochemical Evidence for Magma Mixing and Crustal Contamination in the Post-Collisional Calc-Alkaline Yozgat Volcanics,Central Anatolia,Turkey

Petrographic, major-oxide, and trace-element data are presented for the Yozgat volcanics. These rocks range in composition from basalts through basaltic andesites and andesites to dacites. Major-oxide variations are largely explicable in terms of fractional crystallization, involving removal of observed phenocrysts and microphenocrysts. However, complex zoning patterns and resorbtion phenomena shown by phenocrysts in these lavas, and observed epitaxitic pyroxene growth around quartz xenocrysts imply that they are hybrids formed by a mixing process. In addition, observed enrichments in crustal elements such as K, Rb, Ba, Sr, and P provide clear evidence for the crustal assimilation of granitoid and metasedimentary xenoliths. The following model is suggested for the evolution of the Yozgat volcanics. The primitive magma underwent fractionation in an intracrustal magma chamber to yield more evolved liquids. Influx of hot, primitive magma into the magma chamber promoted vigorous convection-crustal assimilation and eruption of the volcanic rocks in the study area.     

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.     

Recent Volcanism in the Puyehue--Cordon Caulle Region, Southern Andes, Chile (40?5?S): Petrogenesis of Evolved Lavas

Puyehue Volcano (40?5?S) in the southern volcanic zone (33?–46?)of the Andes is a largely basaltic stratovolcano constructedon a highly eroded, dominantly andesitic volcanic center. Duringgrowth of Puyehue Volcano there was a trend from basaltic tomore siliceous lavas, and the most recent eruptions (1921–22,1960) are Cordon Caulle rhyodacites and rhyolites erupted fromfissures northwest of the volcano. These basaltic through rhyoliticlavas define a medium-K₂O suite of tholeiitic affinity withtrace element and Pb-isotopic signatures typical of volcanicrocks associated with subduction zones. Most of the evolved lavas, ranging from andesite to rhyolite,formed by low to moderate pressure ( 5 kb) fractional crystallizationof a plagioclase-dominated anhydrous assemblage. Magma mixingproduced aphyric basaltic andesites with anomalously high incompatibleelement contents and latestage andesites with disequilibriumphenocryst assemblages. The age progression from abundant basaltto younger, less voluminous, more silicic lavas reflects increasinglygreater degrees of fractional crystallization which caused theapparent compositional gap between mixing end members to widen. There is no evidence in the silicic lavas for assimilation ofgeochemically distinctive continental crust. Puyehue basaltsare surprisingly more heterogeneous in ⁸⁷Sr/⁸⁶Sr (0?70378–0?70416)and incompatible element abundance ratios (e.g., La/Sm, Ba/Nb)than the more evolved lavas. This geochemical variability mayreflect subcrustal source heterogeneities or contamination bylower crust. The older basaltic andesites and andesites underlyingthe Puyehue edifice have Sr and Nd isotopic ratios and incompatibleelement abundance ratios within the range of Puyehue basalts.Apparently, similar sources and processes were involved in theirgenesis.     

Primitive andesites from the Taupo Volcanic Zone formed by magma mixing

Andesites with Mg# >45 erupted at subduction zones form either by partial melting of metasomatized mantle or by mixing and assimilation processes during melt ascent. Primitive whole rock basaltic andesites from the Pukeonake vent in the Tongariro Volcanic Centre in New Zealand’s Taupo Volcanic Zone contain olivine, clino- and orthopyroxene, and plagioclase xeno- and antecrysts in a partly glassy matrix. Glass pools interstitial between minerals and glass inclusions in clinopyroxene, orthopyroxene and plagioclase as well as matrix glasses are rhyolitic to dacitic indicating that the melts were more evolved than their andesitic bulk host rock analyses indicate. Olivine xenocrysts have high Fo contents up to 94%, δ¹⁸O_(SMOW) of +5.1‰, and contain Cr-spinel inclusions, all of which imply an origin in equilibrium with primitive mantle-derived melts. Mineral zoning in olivine, clinopyroxene and plagioclase suggest that fractional crystallization occurred. Elevated O isotope ratios in clinopyroxene and glass indicate that the lavas assimilated sedimentary rocks during stagnation in the crust. Thus, the Pukeonake andesites formed by a combination of fractional crystallization, assimilation of crustal rocks, and mixing of dacite liquid with mantle-derived minerals in a complex crustal magma system. The disequilibrium textures and O isotope compositions of the minerals indicate mixing processes on timescales of less than a year prior to eruption. Similar processes may occur in other subduction zones and require careful study of the lavas to determine the origin of andesite magmas in arc volcanoes situated on continental crust.