The andesite aqueduct: perspectives on the evolution of intermediate magmatism in west-central (105–99°W) Mexico

Intermediate calc-alkaline magma (52-65% SiO₂) in western-central Mexico is the focus of this paper, and the typically porphyritic andesites (57-65% SiO₂) form large central volcanoes, whereas basaltic andesites (52-57% SiO₂) are less porphyritic, and they are found as cones and flows but are absent from central volcanoes. Several studies of experimental phase equilibria on these lavas relate water concentration to the phenocryst assemblages and to the degree of crystallinity, so that the abundance, composition and variety of phenocrysts can be used to constrain the amount of water dissolved in the magmas. Thus, the plagioclase-rich andesites of Volcan Colima, Mexico, become so as a result of decompressional crystallisation at ~950 °C (the pyroxene phenocryst temperature), and lose their dissolved water (2.5 to 4.5 wt% H₂O) which is inversely proportional to the modal abundance of plagioclase. The feeding magma to V. Colima, North America's most productive central volcano, is represented by hornblende lamprophyre, a lava type without plagioclase phenocrysts which requires at least 6 wt% water to reproduce the phenocryst assemblage. Thus, degassing of the V. Colima magmas, and of those of the other central volcanoes in the western-central Mexican volcanic belt, contributes essentially all their dissolved water to the conduit or to the atmosphere. The source of this magmatic water is related to the source of the intermediate magmas. For some this must lie in the mantle, as the incorporation of hornblende-lherzolite nodules in a hydrous andesite with hornblende phenocrysts could only have occurred while ascending through the mantle. Consistent with a mantle source is the composition of the olivine phenocrysts in Mexican lavas with 10 to 5% MgO, which is in the mantle range of Fo_88-92. Accordingly, basaltic andesites and andesites with >5% MgO are candidates for a mantle source. The equilibration of intermediate magmas with the mantle, as illustrated by the experiments of various workers, requires that the magmas be hydrous at pressure. An additional constraint is that the activity of silica in the mantle must be equal to that in the hydrous magma at equilibrium. Using published and new experiments to define RTln%_SiO2 in hydrous liquids, this quantity is shown to vary as a function of liquid composition (H₂O, MgO, Na₂O+K₂O), and it approaches zero for quartz-saturated hydrous liquids. Using appropriate values of RTln%_SiO2 for three intermediate lavas, the amount of water required to equilibrate with an olivine-orthopyroxene mantle source is calculated, and within error indicates that only the most silica-rich magma is at water saturation in the mantle, in agreement with published experimental work. Hydrous intermediate magmas, ascending from their hornblende-lherzolite source regions (~1 to 1.5 GPa) along the hydrous adiabat, may not encounter any phase boundaries until 0.2-0.4 GPa because of the increase in the thermal stability of hornblende in water-undersaturated magmas. Therefore, the phenocryst assemblages of hornblende-free andesites equilibrate at low pressures. The virtual absence of basalt in west-central Mexico (<4 Ma) is considered to be related to the large increase in crystallinity found in isobaric hydrous experiments crystallising hornblende at pressures close to those at the base of the crust. As a large proportion of the ferromagnesian components of basalt is acceptable to hornblende, it does not take a significant cooling interval (~40-50 °C) below the liquidus for hydrous basaltic magma to acquire >50% crystallinity, evidently also an eruptible limit for V. Colima andesitic lavas. If the lower limit of water dissolved in Mexican intermediate magmas is accepted as that required for phenocryst equilibration (~6 wt% water), and the upper limit as saturation in the mantle source at 1 GPa (~16 wt%) then, with an estimate of the volcanic and plutonic magma delivery rate (km³/10⁶ year) per km of volcanic arc, the flux of water returned from the mantle along the 35,000-km, global subduction-related arc system can be estimated. Measurements of the volcanic flux are woefully few, and estimates from Mexico, the Lesser Antilles and central America show a range from 4 to 20 km³/10⁶ year2km which, if subtracted from the isotopically constrained continental growth rate, gives the plutonic flux rate. This suggests that, of the magma flux ascending to the continental crust, only about a fifth reaches the surface. If the dissolved magmatic water limits are coupled with the volcanic and plutonic emplacement rates, then the amount of water returned by magmatism to the crust is crudely in balance with that subducted.     

Manam Island, Papua New Guinea: Petrology and Geochemistry of a Low-TiO2 Basaltic Island-Arc Volcano

Manam volcano consists of relatively mafic and compositionallysimilar tholeiitic basalts and low-SiO₂ andesites that are characterizedby notably low (mainly 0?3–0?35 weight per cent) TiO₂contents. These rocks provide an ideal opportunity to investigateboth the extent of depletion in their peridotite magma-sourceregions (which are evidently similar in many respects to thehighly depleted sources of boninitic magmas), and the interplayof the high-level processes of magma mixing, crystal fractionation,and upper crustal contamination, in an island-are volcano. Manamrocks have pronounced enrichments in Rb, Ba, K, and Sr relativeto the light rare-earth elements and, especially, to the high-field-strengthelements (Sr/Ti values are exceptionally high). However, thereis no compelling evidence that these enrichments were causedby addition of a hydrous, slab-derived component to the peridotitesource region. Nd and Sr-isotope ratios plot within the oceanicmantle array; ²⁰⁷Pb/²⁰⁴Pb values are only slightly higher thanthose for oceanic rocks; and the absence of hydrous minerals,the early crystallization and modal preponderance of plagioclaseover pyroxene, high estimated quenching temperatures, and lowwater contents in the Manam rocks, are all evidence that themagmas crystallized under markedly water-undersaturated conditions.Unusually anorthite-rich plagioclase phenoerysts in the morediffrentiated rocks may correspond to crystallization underhigher water-vapour pressures, possibly caused by influxes ofgroundwater, or they may be accidental xenocrysts. Fractionationof olivine, clinopyroxene, and spinel (early chromite followedby magnetite) has dominated the evolution of the magma series.However, clear correlations between incompatible trace-elementratios, ⁸⁷Sr/⁸⁶Sr, and 100 Mg/(Mg ? Fe^2?) values are convincingevidence for an accompanying mixing process—either of(1) two basaltic magma types (one more fractionated and lowerin ⁸⁷Sr/⁸⁶Sr than the other), or (2) pristine magmas and contaminantfrom basaltic conduit and reservoir wall rocks. Wall-rock contaminationis the less likely process, and is the more difficult one toidentify, particularly if it accompanied magma mixing.     

A petrological study of the younger Tongan andesites and dacites,and the olivine tholeiites of Niua Fo'ou Island,S. W. Pacific

Basaltic andesites are the dominant Tongan magma type, and are characterized by phenocrysts of augite, orthopyroxene (or rarely pigeonite), and calcic plagioclase (modally most abundant phase, and interpreted as the liquidus phase). The plagioclase phenocrysts exhibit slight oscillatory reverse zoning except for abrupt and thin more sodic rims, which are interpreted to develop during eruptive quenching. These rim compositions overlap those of the groundmass plagioclase. The pyroxene phenocrysts also exhibit only slight compositional zoning except for the outermost rim zones; the compositions of these rims, together with the groundmass pyroxenes, vary throughout the compositional range of subcalcic augite to ferroaugite through pigeonite to ferropigeonite, and are interpreted in terms of quench-controlled crystallization. This is supported, for example, by the random distribution of Al solid solution in the groundmass pyroxenes, compared to the more regular behaviour of Al in the phenocryst pyroxenes. The analysed Niua Fo'ou olivine tholeiites are aphyric; groundmass phases are plagioclase (An_17–88), olivine (Fa_18–63), titanomagnetite (usp. _59–73), and augite-ferroaugite which does not extend to subcalcic compositions; this is interpreted to be due to higher quenching temperatures and lower viscosities of these tholeiites compared to the basaltic andesites.Application of various geothermometers to the basaltic andesites suggest initial eruptive quenching temperatures of 1,008–1,124 ° C, plagioclase liquidus temperatures (1 bar) of 1,210–1,277 ° C, and orthopyroxene-clinopyroxene equilibration of 990–1,150 ° C. These calculated temperatures, together with supporting evidence (e.g. absence of olivine and amphibole, liquidus plagioclase, and plagioclase zoning patterns) are interpreted in terms of phenocryst crystallization from magmas that were either strongly water undersaturated, nearly anhydrous, or at best, water saturated at very low pressures (< 0.5 kb). This interpretation implies that these Tongan basaltic andesites did not originate by any of the currently proposed mechanisms involving hydrous melting within or above the Benioff zone.     

Ascent-driven crystallisation of dacite magmas at Mount St Helens, 1980–1986

We introduce a novel scheme that enables natural silicic glasses to be projected into the synthetic system Qz-Ab-Or-H₂O in order to relate variations in volcanic glass chemistry to changing pressure (P) and temperature (T) conditions in the sub-volcanic magma system. By this means an important distinction can be made between ascent-driven and cooling-driven crystallisation under water-saturated or undersaturated conditions. In samples containing feldspar and a silica phase (quartz or tridymite), quantitative P-T estimates of the conditions of last equilibrium between crystals and melt can be made. Formation of highly silicic melts (i.e. >77 wt% SiO₂) is a simple consequence of the contraction of the silica phase volume with decreasing pressure, such that high silica glasses can only form by crystallisation at low pressure. Resorption of quartz crystals appears to be a further diagnostic feature of decompression crystallisation. Groundmass and inclusion glasses in dacites from the 1980-1986 eruption of Mount St Helens volcano (WA) span a wide range in SiO₂ (68-80 wt%, anhydrous). The compositions of the least evolved (SiO₂-poor) inclusions in amphibole phenocrysts record entrapment of silicic liquids with Е.4 wt% water, corresponding to a water saturation pressure of ~200 MPa at 900 °C. The compositions of more evolved (higher SiO₂) plagioclase-hosted inclusions and groundmass glasses are consistent with extensive ascent-driven fractional crystallisation of plagioclase, oxide and orthopyroxene phenocrysts and microlites to low pressures. During this polybaric crystallisation, plagioclase phenocrysts trapped melts with a wide range of dissolved water contents (3.5-5.7 wt%). Magmas erupted during the Plinian phase of the 18 May 1980 eruption were derived from a large reservoir at depths of ̈́ km. Subsequent magmas ascended to varying depths within the sub-volcanic system prior to extraction. From glass chemistry and groundmass texture two arrest levels have been identified, at depths of 0.5-1 and 2-4 km. A single dome sample from February 1983 contains groundmass plagioclase, tridymite and quartz, testifying to temperatures of at least 885 °C at 11 MPa. These shallow storage conditions are comparable to those in the cryptodome formed during spring 1980. The corresponding thermal gradient, А.2 °C MPa^-1, is consistent with near-adiabatic magma ascent from ~8 km. We argue that the crystallisation history of Mount St Helens dacite magma was largely a consequence of decompression crystallisation of hot magma beyond the point of water saturation. This challenges the conventional view that phenocryst crystallisation occurred by cooling in a large magma chamber prior to the 1980-1986 eruption. Because the crystallisation process is both polybaric and fractional, it cannot be simulated directly using isobaric equilibrium crystallisation experiments. However, calculation of the phase proportions in water-saturated 910ᆣ °C experiments by Rutherford et al. (1985) over the pressure range 220-125 MPa reproduces the crystallisation sequence and phenocryst modes of Mount St Helens dacites from 18 May 1980. By allowing for the effects of fractional versus equilibrium crystallisation, entrained residual source material, and small temperature differences between nature and experiment, phase compositions can also be matched to the natural samples. We conclude that decompression of water-saturated magma may be the dominant driving force for crystallisation at many other silicic volcanic centres.     

The Arc Lavas of the Shirahama Group, Japan: Sr and Nd Isotopic Data Indicate Mantle-Derived Bimodal Magmatism

New Sr and Nd isotopic data are presented and integrated withprevious data for the Shirahama Group Mio-Pliocene medium-Kvolcanic are suite of south-central Honshu, Japan. Main resultsare: (1) The Shirahama lavas range in ⁸⁷Sr/⁸⁶Sr from 0.70315to 0.70337 and in ¹⁴³Nd/¹⁴⁴Nd from 0.51298 to 0.51306; the Srand Nd isotopic data cluster tightly within the mantle array,and all lie within an overlapping field of mid-ocean ridge basaltand ocean island basalt; (2) small differences exist among theShirahama tholeiitic series, calc-alkaline series and mixedlavas. The present isotopic data are consistent with a previouslypublished model, which proposes that chemical variations inmagmas of coexisting tholeiitic and calc-alkaline series areproduced through crystal fractionation from mantle-derived magmasof basalt and magnesian andesite, respectively. Moreover, thetholeiitic series and the calc-alkaline series are isotopicallyidentical. Thus, both magma series can be derived from a sourcemantle with the same isotopic composition, supporting the hypothesisof simultaneous generation of basalt and magnesian andesitemagmas from a single diapir rising through the mantle wedgeabove the subduction zone. The differences of water contentand temperature within the diapir are again thought to havebeen produced through dehydration and heating of an isotopicallyhomogeneous hydrous diapir. The isotopic data show that thehigh-SiO₂ lavas have the same isotopic compositions as moremafic lavas. These data and liquid lines of descent of the Shirahamamagmas suggest that even rhyolites can be produced by differentiationfrom mantle-derived magmas without crustal contamination. Analysesfrom 38 other arc volcanoes have been compiled to investigatethe intravolcano variability of ⁸⁷Sr/⁸⁶Sr. Twelve of these displayno intravolcano strontium isotopic variability, as is the casewith the Shirahama Group, but others show greater variationof ⁸⁷Sr/⁸⁶Sr from individual volcanic centers, presumably reflectingcrustal contamination. Most of the latter volcanoes are underlainby thick continental crust. It is noteworthy, however, thatthe greater variations of ⁸⁷Sr/⁸⁶Sr correlate with SiO₂ content;andesites or dacites, not basalts, from the same volcano havethe lowest ⁸⁷Sr/⁸⁶Sr, and these rocks are calc-alkaline in termsof FeO^*/MgO and SiO₂ Theoretically, assimilation of continentalcrust by the isotopically uniform Shirahama magmas could producethese relationships. Given that mantle-derived basalt and magnesianandesite both encounter continental crust on their ascent tothe surface, the hotter basalt magma would assimilate more crustalwallrocks than the cooler andesite, resulting in the basaltbeing more radiogenic. Fractional crystallization, magma mixing,and/or assimilation-fractional crystallization of these magmasin crustal magma chambers could produce large compositionalvariations, but the derivatives of the hotter basaltic magmas(tholeiitic series in the broad sense) would display greatercontamination than those derived from the cooler andesitic magmas(calc-alkaline series). ^*Telephone: 81-858-43-1215. Fax: 81-858-43-2184. e-mail: tamura{at}misasa.okayam-u.ac.jp     

Water content of primitive low-K tholeiitic basalt magma from Iwate Volcano,NE Japan arc: implications for differentiation mechanism of frontal-arc basalt magmas

The water content of low-K tholeiitic basalt magma from Iwate volcano, which is located on the volcanic front of the NE Japan arc, was estimated using multi-component thermodynamic models. The Iwate lavas are moderately porphyritic, consisting of ~8 vol.% olivine and ~20 vol.% plagioclase phenocrysts. The olivine and plagioclase phenocrysts show significant compositional variations, and the Mg# of olivine phenocrysts (Mg#78–85) correlates positively with the An content of coexisting plagioclase phenocrysts (An_85–92). The olivine phenocrysts with Mg# > ~82 do not form crystal aggregates with plagioclase phenocrysts. It is inferred from these observations that the phenocrysts with variable compositions were primarily derived from mushy boundary layers along the walls of a magma chamber. By using thermodynamic calculations with the observed petrological features of the lavas, the water content of the Iwate magma was estimated to be 4–5 wt.%. The high water content of the magma supports the recent consensus that frontal-arc magmas are remarkably hydrous. Using the estimated water content of the Iwate magma, the water content and temperature of the source mantle were estimated. Given that the Iwate magma was derived from a primary magma solely by olivine fractionation, the water content and temperature were estimated to be ~0.7 wt.% and ~1,310 °C, respectively. Differentiation mechanisms of low-K frontal-arc basalt magmas were also examined by application of a thermodynamics-based mass balance model to the Iwate magma. It is suggested that magmatic differentiation proceeds primarily through fractionation of crystals from the main molten part of a magma chamber when it is located at <~200 MPa, whereas magma evolves through a convective melt exchange between the main magma and mushy boundary layers when the magma body is located at >~200 MPa.     

Compositional relations of coexisting orthopyroxene,pigeonite and augite in a tholeiitic andesite from Hakone Volcano

The compositions of five different coexisting pyroxenes hypersthene, pigeonite and augite in groundmass and bronzite and augite of phenocryst in a tholeiitic andesite from Hakone Volcano, Japan have been determined by the electron probe microanalyser. It is shown that there is a compositional gap of about 25 mole per cent CaSiO₃ between groundmass pigeonite and augite, compared with 35 per cent CaSiO₃ between phenocrystic augite and bronzite. Subcalcic augite or pigeonitic augite was not found. The groundmass augite, which occurs only as thin rims of pigeonite and hypersthene, is less calcic and more iron-rich than the phenocryst augite. It is also shown that the groundmass pigeonite is 3–4 mole per cent more CaSiO₃-rich than the coexisting groundmass hypersthene. The Fe/(Mg + Fe) ratios of these coexisting hypersthene and pigeonite are about 0.31 and 0.33, respectively. It is suggested from these results that a continuous solid solution does not exist between augite and pigeonite of the Fe/(Mg + Fe) ratio at least near 0.3 under the conditions of crystallization of groundmass of the tholeiitic andesite. It is suggested from the Mg-Fe partition and the textural relation that the groundmass augite crystallized from a liquid more iron-rich than that from which groundmass hypersthene and pigeonite crystallized.     

Effect of Water on the Composition of Magmas Formed at High Pressures

Portions of the system MgO-CaO-Na₂O-Al₂O₃-SiO₂-H₂O have beenstudied in the pressure range 13–35 kb at near-liquidustemperatures. The liquidus field of forsterite relative to thatof orthopyroxene is considerably wider under anhydrous thanunder anhydrous conditions and it covers part of the plane ofsilica-saturation in a wide pressure range. Partial meltingof simple garnet lherzolite (= forsterite+orthopyroxene+clinopyroxene+garnet)with water produces quartz-normative liquids at pressures upto at least 25 kb regardless of water content. Hydrous mineralsare not encountered at or near the solidus temperatures exceptin a Na-rich part of the system. Microprobe analysis of therun products in this synthetic system shows that the liquid(glass) in equilibrium with the lherzolite mineral assemblageis silica and alumina-rich at 20 kb under vapor-present conditions.With increasing degree of partial melting, the liquid changesits composition, passing into a ‘vapour-absent region’and becoming less silicic. Fractional crystallization of olivinetholeiitic magma under hydrous conditions also produces silica-richmagmas at high pressures. If the system is open to water, andwater pressure is less than total pressure, the compositionof the liquid varies from quartz-normative to olivine (±nepheline)-normativedepending on water pressure. It is suggested that in the presenceof water, silica-rich magmas such as those of calc-alkalic andesiteor dacite may be formed by direct partial melting of the peridotiticupper mantle at depths down to about 80 km. A large degree ofpartial melting of lherzolite under hydrous conditions wouldproduce SiO2 and MgO-rich magmas. The clinoenstatite rock fromCape Vogel, Papua, may have been formed by such a process. Peridotiteswith low CaAl2SiO5/jadeite ratios in the clinopyroxene couldproduce nepheline-normative magma by small degree of partialmelting and tholeiitic magma by large degree of partial meltingunder hydrous conditions.     

Klyuchevskoy Volcano, Kamchatka, Russia: The Role of High-Flux Recharged, Tapped, and Fractionated Magma Chamber(s) in the Genesis of High-Al2O3 from High-MgO Basalt

Mineral Chemistry, and major and trace element variations ofthe basalts from Klyuchevskoy, the world's most active islandare volcano, are most consistently explained by the persistenceof a non-steady state, erupting, recharging, and fractionatingmagma chamber in which fractionation of a parental high-MgObasalt melt produces high-Al₂O₃ basalt. Although fractionalcrystallization is the dominant controlling mechanism, periodicrecharge with a more primitive high-MgO basalt is also an importantprocess contributing to the chemical evolution of the magmas.Hybrid basalts are the mixed product of high-Al₂O₃ basalt rechargedwith high-MgO basalt. The lavas range in composition from high-MgO, low-Al₂O₃ ( 12wt. % MgO, 14 wt. % Al₂O₃) to high-Al₂O₃, low-MgO ( 18 wt. %Al₂O₃, 4 wt. % MgO). The high-MgO lavas are characterized byphenocrysts of olivine (cores FO_90–80 and rims FO_85–75)with chromite inclusions [Cr/(Cr + Al)0.7], clinopyroxene (Wo_46–42En_48–42Fs_15–7),and the rare occurrence of orthopyroxene (En_72–70). Allthe phenocrysts are normally zoned and set in a groundmass ofplagioclase, pigeonite, clinopyroxene, magnetite, orthopyroxene.The high-Al₂O₃ basalts contain plagioclase (An_85–55),olivine (Fo_80–65), clinopyroxene (Wo_45–30En_50–38Fs_23–11), orthopyroxene (En_72–70) phenocrysts, that preserve bothnormal and reverse zoning in a groundmass of plagioclase, pigeonite,olivine, clinopyroxene, magnetite, orthopyroxene. Hybrid basaltshave characteristics of both high-MgO basalts and high-Al₂O₃basalts and preserve complicated normal-to-reverse, reverse-to-normal,and normally zoned phenocrysts. No hydrous minerals are presentin any of the lavas. The varied basaltic magmas erupted from Klyuchevskoy are derivedfrom a magma chamber(s) located near the base of the Kamchatkacrust (pressures 0.5–0.9 GPa) and characterized by relativelyhigh crystallization temperatures, some in excess of 1150C.Under these conditions, the fractionation of a parental high-MgOmagma, produced principally from the melting of a fluid-fluxed,peridotitic mantle wedge, results in the production of a chemicallydiverse spectrum of basalts ranging from high-MgO, low-Al₂O₃to high-Al₂O₃, low-MgO basalt, traversing the relatively primitiveend of both the calc-alkalic and tholeiitic differentiationtrends.     

Compositional and Dynamic Controls on Mafic--Silicic Magma Interactions at Continental Arc Volcanoes: Evidence from Cordn El Guadal, Tatara-San Pedro Complex, Chile

Heterogeneous andesitic and dacitic lavas on Cordn El Guadalbear on the general problem of how magmas of differing compositionsand physical properties interact in shallow reservoirs beneathcontinental arc volcanoes. Some of the lavas contain an exceptionallylarge proportion (<40%) of undercooled basaltic andesiticmagma in various states of disaggregation. Under-cooled maficmagma occurs in the silicic lavas as large (<40 cm) basalticandesitic magmatic inclusions, as millimeter-sized crystal-clotsof Mg-rich olivine phenocrysts plus adhering Carich plagioclasemicrophenocrysts (An_50–70), and as uniformly distributed,isolated phenocrysts and microphenocrysts. Compositions andtextures of plagioclase phenocrysts indicate that inclusion-formingmagmas are hybrids formed by mixing basaltic and dacitic melts,whereas textural features and compositions of groundmass phasesindicate that the andesitic and dacitic lavas are largely mechanicalmixtures of dacitic magma and crystallized basaltic andesiticmagma. This latter observation is significant because it indicatesthat mechanical blending of undercooled mafic magma and partiallycrystallized silicic magma is a possible mechanism for producingthe common porphyritic texture of many calc-alkaline volcanicrocks. The style of mafic-silicic magma interaction at CordonEl Guadal was strongly dependent upon the relative proportionsof the endmembers. Equally important in the Guadal system, however,was the manner in which the contrasting magmas were juxtaposed.Textural evidence preserved in the plagioclase phenocrysts indicatesthat the transition from liquid-liquid to solid-liquid mixingwas not continuous, but was partitioned into periods of magmachamber recharge and eruption, respectively. Evidently, duringperiods of recharge, basaltic magmas rapidly entrained smallamounts of dacitic magma along the margins of a turbulent injectionfountain. Conversely, during periods of eruption, dacitic magmagradually incorporated small parcels of basaltic andesitic magma.Thus, the coupled physical-chemical transition from mixed inclusionsto commingled lavas is presumably not coincidental. More likely,it probably provides a partial record of the dynamic processesoccurring in shallow magma chambers beneath continental arevolcanoes. KEY WORDS: Chile; commingling; magma mixing; magmatic inclusions ^*Present address: Department of Earth Sciences, Montana State University, Bozeman, MT 59717, USA     

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     

Liquid Lines of Descent of Island Arc Magmas and Genesis of Rhyolites: Evidence from the Shirahama Group, Japan

The Mio-Pliocene Shirahama Group, Izu Peninsula, Central Japan,a well-exposed submarine volcanic arc complex of lava flows,pyroclastic rocks and associated shallow intrusives, is characterizedby a tholeiitic series (basalt to dacite) and a calc-alkalineseries (andesite to dacite). Chemical variations in the tholeiiticseries and calc-alkaline series are consistent with crystalfractionation from basalt and magnesian andesite (boninite),respectively. Crystal–liquid phase relations of thesemagmas have been investigated by study of sample suites fromthese two series. Compositions of liquids in equilibrium withphenocrysts were determined by microprobe grid analyses, inwhich 49 points were averaged in 03 mm 03 mm groundmassareas. The liquid compositions, coupled with the phenocrystmineralogy of the same samples, define the liquid lines of descentof these volcanic arc magmas. Major findings include the following:(1) Crystallization of the tholeiitic series magma is consistentwith early stage crystallization in the simple system Fo–Di–Silica–H₂O,with olivine having a reaction relation to augite and the tholeiiticliquid. (2) The later stage products of the tholeiitic seriesmagma are, however, crystal-poor (<10%) dacites with no maficminerals, suggesting that tholeiitic liquids, hypersthene andaugite were no longer on the cotectic (3) A characteristic ofthe calc-alkaline series magmas is the development of rhyoliticliquids. Hypersthene, augite, plagioclase and Fe–Ti oxideoccur in most calc-alkaline rocks studied, and hornblende andquartz can be found in about half of these. However, their differentiationpaths show that the cotectic relation between quartz and liquidended at a later stage, resulting in the resorption of quartzphenocrysts and ultimately in the formation of quartz-free magmas.(4) The late-stage liquids of both the tholeiitic and calc-alkalineseries have deviated from their cotectics, which cannot be explainedby fractional crystallization alone. The addition of H₂O froman outside system is probably required to explain the differentiationpaths. (5) The formation of chilled margins, the in situ crystallizationof a magma chamber in the solidification zone, and/or the migrationof groundwater into the magma chamber are thought to be likelyprocesses affecting magmas during their migration and intrusioninto the crust. An extreme effect of H₂O addition would be tolower the liquidus temperatures of all precipitating silicatephases far below their restorable range before eruption, resultingin the production of aphyric magmas. Even when a temperaturedecrease in the magma chamber causes a liquid to intersect theliquidus of a pre-existing phase, the addition of H₂O shiftsthe cotectic toward SiO₂, resulting in quartz being the lastphase to crystallize. The resorption of quartz is interpretedto be the result of a liquidus boundary shift caused by theaddition of H₂O. The genesis of aphyric rhyolites is thereforeinferred to result from fractional crystallization followingaddition of H₂0. KEY WORDS: Shirahama Group; Japan; island arc; rhyolite; magma series     

Mineralogy and Petrogenesis of the Deccan Trap Lava Flows around Mahabaleshwar, India

Electron microprobe analyses of minerals of thirteen DeccanTrap lava flows at Mahabaleshwar have been carried out in thepresent study. All of these flows have tholeiitic bulk compositionsand all, except one (represented by MB-81-17 of Mahoney et al.,1982) contain olivine, plagioclase, two pyroxenes, and Fe-Tioxide minerals. Olivine and plagioclase appear as distinct phenocrystsin all but one flow, and Ca-rich pyroxene joins as a phenocrystphase in the younger flows. Pigeonite and Fe-Ti oxide minerals(titanomagnetite and ilmenite) occur in the groundmass. Olivineoccurs as both groundmass and phenocryst phase in MB-81-17 (whichis the only flow without low-Ca pyroxene phase); in all otherflows olivine appears only as phenocryst phase. In all but one(MB-81-17) flow olivine is completely altered. MB-81-17 olivinegrains are only partly altered, and in this rock the cores ofphenocrysts are rounded and have a composition of Fo₇₇ whereastheir euhedral rims have a composition around Fo₆₇. The groundmassolivine grains in MB-81-17 are Fo_41–32. Substantial Fe-enrichmentand zoning trends are shown by the pyroxenes in individual rocks.The cores of Ca-rich pyroxene phenocrysts of some of the flowshave as much as 4 wt. per cent A1₂O₃ and may have crystallizedat higher (crustal) pressures. Pigeonite thermometry (Ishii,1975) suggests an average of 1050?C for crystallization of thegroundmass pigeonite (eruption temperature?). Fe-Ti oxide mineralsare mostly altered in the older flows. In the younger flows,coexisting unaltered titanomagnetite and ilmenite yield maximumtemperature estimates for the crystallization of these phaseof about 1025?C and an oxygen fugacity of 10^–11.5 atm.The T-fo₂ path followed by these flows seems to have been consistentlysomewhat lower than that defined by the 1 atm. fayalite-magnetitequartz curve. All of the lavas examined have experienced extensivefractional crystallization of olivine and some clinopyroxeneat relatively higher pressures. These lavas were saturated orclose to being saturated with olivine+plagioclase+clinopyroxeneduring eruption. Plagioclase accumulation, although it appearsto have occurred, has not been significant. It is suggestedthat MB-81-17 magma was contaminated by a calcite-rich rock(limestone?) whereas the lower Group 1 magmas may have beenselectively contaminated by quartz-bearing contaminant. Alternately,parental magma of MB-81-1 (with the highest Mg-number and 8= -16) may have been produced in the upper mantle into whichminor masses of old crust was well mixed. Magma mixing, crystalfractionation, and contamination processes of Mahabaleshwarbasalts and possible genetic relationships with other DeccanTrap lavas are discussed.     

Petrological imaging of an active pluton beneath Cerro Uturuncu,Bolivia

Uturuncu is a dormant volcano in the Altiplano of SW Bolivia. A present day ~70 km diameter interferometric synthetic aperture radar (InSAR) anomaly roughly centred on Uturuncu’s edifice is believed to be a result of magma intrusion into an active crustal pluton. Past activity at the volcano, spanning 0.89 to 0.27 Ma, is exclusively effusive and almost all lavas and domes are dacitic with phenocrysts of plagioclase, orthopyroxene, biotite, ilmenite and Ti-magnetite plus or minus quartz, and microlites of plagioclase and orthopyroxene set in rhyolitic groundmass glass. Plagioclase-hosted melt inclusions (MI) are rhyolitic with major element compositions that are similar to groundmass glasses. H₂O concentrations plotted versus incompatible elements for individual samples describe a trend typical of near-isobaric, volatile-saturated crystallisation. At 870 °C, the average magma temperature calculated from Fe–Ti oxides, the average H₂O of 3.2 ± 0.7 wt% and CO₂ typically <160 ppm equate to MI trapping pressures of 50–120 MPa, approximately 2–4.5 km below surface. Such shallow storage precludes the role of dacite magma emplacement into pre-eruptive storage regions as being the cause of the observed InSAR anomaly. Storage pressures, whole-rock (WR) chemistry and phase assemblage are remarkably consistent across the eruptive history of the volcano, although magmatic temperatures calculated from Fe–Ti oxide geothermometry, zircon saturation thermometry using MI and orthopyroxene-melt thermometry range from 760 to 925 °C at NNO ± 1 log. This large temperature range is similar to that of saturation temperatures of observed phases in experimental data on Uturuncu dacites. The variation in calculated temperatures is attributed to piecemeal construction of the active pluton by successive inputs of new magma into a growing volume of plutonic mush. Fluctuating temperatures within the mush can account for sieve-textured cores and complex zoning in plagioclase phenocrysts, resorption of quartz and biotite phenocrysts and apatite microlites. That Fe–Ti oxide temperatures vary by ~50–100 °C in a single thin section indicates that magmas were not homogenised effectively prior to eruption. Phenocryst contents do not correlate with calculated magmatic temperatures, consistent with crystal entrainment from the mush during magma ascent and eruption. Microlites grew during ascent from the magma storage region. Variability in the proportion of microlites is attributed to differing ascent and effusion rates with faster rates in general for lavas >0.5 Ma compared to those <0.5 Ma. High microlite contents of domes indicate that effusion rates were probably slowest in dome-forming eruptions. Linear trends in WR major and trace element chemistries, highly variable, bimodal mineral compositions, and the presence of mafic enclaves in lavas demonstrate that intrusion of more mafic magmas into the evolving, shallow plutonic mush also occurred further amplifying local temperature fluctuations. Crystallisation and resorption of accessory phases, particularly ilmenite and apatite, can be detected in MI and groundmass glass trace element covariation trends, which are oblique to WRs. Marked variability of Ba, Sr and La in MI can be attributed to temperature-controlled, localised crystallisation of plagioclase, orthopyroxene and biotite within the evolving mush.     

Compositional Zoning in Pyroxenes from Lunar Rock 12021, Oceanus Procellarum

Electron probe study of the pyroxene phenocrysts in rock 12021of the Apollo 12 sample reveals an extraordinary variety ofzoning phenomena. These phenocrysts have cores of relativelyhomogeneous pigeonite which are mantled by Ca-rich pyroxenes;the mantles are zoned outward from about 20 mol per cent FeSiO₃at the core-mantle boundaries to 70 mol per cent FeSiO₃ at themargins of the phenocrysts. The character of the normal zoningdiffers in each growth sector. Four different trends characterizinggrowth on (110), (100), (010), and parallel to c are described.Pronounced but erratic oscillatory effects are impressed onthe normal zoning in all sectors. Normal zoning in lunar pyroxenes is generally more extensivethan in terrestrial pyroxenes, probably because the lunar lavaswere an order of magnitude more fluid than terrestrial basalts.Turbulent flow in lunar lavas may have caused some of the oscillatoryeffects. The cyclic nature of augite and pigeonite crystallizationin these pyroxenes is probably kinetic in origin; conceivablyit could reflect the presence of an augite-pigeonite peritectic.It is likely that further knowledge of the crystal structureof pigeonite at high temperatures will be required before astructural model can be formulated that will satisfactorilyexplain the details of the sector zoning. Coarse-grained pyroxferroite and subcalcic ferroaugite havecrystallized in apparent ‘equilibrium’ in the finalstages of formation of the groundmass in rock 12021. Nevertheless,the crystallization of the pyroxferroite was probably metastablerelative to the assemblage ferroaugite+ fayalite+ tridymite.Data on the effect of Mg substitution on the stability of pyroxferroitewill be needed to establish this point. We suggest that the pigeonite cores of the phenocrysts in rock12021 crystallized under quiescent conditions, probably in amagma chamber below the lunar surface, and that the stronglyzoned augite mantles crystallized during emplacement of thelava on the surface.     

Petrogenesis of Victorian Cambrian Tholeiites and Implications for the Origin of Associated Boninites

In Victoria, tholeiitic basalts and subvolcanic dolerites andgabbros in the Heatheote and Mount Wellington Greenstone Beltsoccur stratigraphically above boninites, and in the latter beltcontain interbedded arc-derived andesitic detritus. Intrusiverocks form concordant, sill-like bodies up to 1 km thick whichare often strongly differentiated, chemically and mineralogically.The volcanic section in both greenstone belts, between 1000and 1500m thick, is dominated by aphyric or sparsely augitephyrictholeiites which trend toward ferrotholeiite compositions andare comagmatic with underlying intrusives. The tholeiites are a low-K₂O suite with chondritic REE patterns,initial _Nd= +4?5 to +5?0, and trace element characteristicsmost like those shown by modern basalts erupted during the earlieststages of arc rifting and backarc basin opening. From virtuallyidentical parental magmas, the basalts in the Heathcote GreenstoneBelt show a very rapid increase in TiO₂, Zr, Y, and La withincreasing differentiation relative to those in the Mount WellingtonGreenstone Belt. This is explained using O'Hara's (1977) modelfor open system fractionation, in which magma supply and eruptionrate is significantly higher for the Heathcote belt magma chambers. The proposed petrogenetic model for the Victorian Cambrian tholeiitesinvolves subduction of an oceanic spreading centre beneath anearly Cambrian forearc region. Continued magma generation atthe subducted spreading centre resulted in diapirs of 1400?CMORB-source mantle piercing into the over-riding plate and providingheat to locally generate boninites from shallow, refractory,hydrous upper mantle beneath the forearc. Subsequent partialmelting of the MORB-source diapirs yielded tholeiitic magmas,which ascended to erupt upon the very slightly older boninites,and eventually split the arc and open a backarc basin as magmasupply became more voluminous. In this forearc setting, thesource-to-eruption crustal thickness through which the earliesterupted tholeiites had to traverse was notably greater thanat typical spreading centres, and basaltic magmas were ableto differentiate through to ferrobasaltic compositions. Theboninite-tholeiite sections of the Heathcote and Mount WellingtonGreenstone Belts are therefore considered to represent a recordof the earliest stages of magrnatism accompanying ridge subductionand splitting of an arc to form a backarc basin.     

Major Addition of Magma at the Pyroxenite Marker in the Western Bushveld Complex, South Africa

A major, but gradual, reversal in the cryptic variation patternof the plagioclase and pyroxenes, of 13 mol% anorthite and 10mol% Mg/ (Mg + Fe) respectively, is documented in the Main Zoneof the western Bush veld Complex. These changes are accompaniedby a decrease in initial ⁸⁷Sr/⁸⁶Sr ratio from > 0.708 to< 0.707. The Pyroxenite Marker, a distinctive orthopyroxenitelayer, occurs close to the top of this reversed differentiationsequence. This is attributed to addition of less differentiatedmagma. On the basis of a mass balance calculation of the initial⁸⁷Sr/ ⁸⁶Sr ratios, it is estimated that the volume of magmaadded was comparable to that of the resident magma. Increases in the Fe₂O₃, TiO₂, Al₂O₃, and Na₂O contents of thepyroxenes above the level of magma addition indicate that thenew magma had a lower silica activity and higher fO₂ than theresident magma. Quantification of the trace element and REEcontent of the two magmas is hampered by the very low proportionof trapped intercumulus component in these adcumulate rocks.However, semi-quantitative modelling indicates that the traceand REE signatures of the two magmas were similar, with moderateLREE enrichment and flat HREE profiles. The new magma had aslightly higher La/ Sm ratio than the resident magma, consistentwith its more alkaline nature. The new magma was probably added gradually, while 100–150m of cumulates formed. It probably intruded at an intermediatelevel within an existing stratified magma chamber, where itcooled and crystallized, and composite packets of liquid pluscrystals plunged to the base of the chamber. The cores of plagioclasegrains formed during this mixing interval show a wider rangeof compositions than in other sections, and plagioclase primocrystsfrom both magmas may be preserved within single samples. Therefore,although intimate physical mixing of packets of unknown sizeof the two magmas occurred, re-equilibration of the major oxidecomposition of the plagioclase primocrysts was not achieved.However, the data and calculations based on diffusion ratesindicate that partial Sr isotopic resetting of plagioclase mayhave occurred.     

Low-Pressure Experimental Constraints on the Evolution of Komatiites

Melting experiments were performed on a komatiitic basalt with17 wt% MgO from Munro Township, Ontario, at I-atm pressure andan oxygen fugacity controlled approximately to the fayalite-magnetite-quartzbuffer. The experiments showed that olivine appears at 1344±5°C,spinel at 1334±6°C plagioclase at 1185±5°C,augite at 1176±5°C and pigeonite at 1154±6°C.Compositionally, olivine varies from Fo₉₀ to Fo₇₄ and displaysan average K^Fe/Mg_D (ol/liq) of 0•32. The spinels are chromitesand chromian spinels with Mg/(Mg + Fe²⁺) ratios between 0•66and 0•;32, which show a marked correlation with meltingtemperature. The pyroxenes show an average K^Fe/Mg_D (px/liq)of 0•26, identical for augite and pigeonite. Plagiodaseranges compositionally between An₈₂ and An₇₂ Plotted in thepseudo-quaternary basalt phase diagram, the liquid line of descentis similar to that observed for quartz tholeiitic magmas. Therefore,the low-pressure, late-stage evolution products of komatiiteand basaltic komatiite parental magmas will chemically and mineralogicallybe ferrobasaltic quartz tholeiites. High-temperature and high-pressuremodeling suggests that the main observed compositional variationof Munro komatiites can be explained by low-pressure crystalfractionation and accumulation of olivine into komatiite liquidswith below 21•5–23•5 wt% MgO and eruptive temperaturesbelow 1435–1465°C for oxygen fugacities between thefayalite-magnetite quartz (FMQ) and iron-wiistite (IW) buffers.The maximum magnesium content of liquid komatiites, assumingequilibrium Fo₉₄ olivine, is 27–29 wt% MgO and eruptivetemperatures are between 1515 and 1540°C. KEY WORDS: komatiites; experimental petrology; Munro Township; Ontario     

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.     

The Occurrence of Forsterite and Highly Oxidizing Conditions in Basaltic Lavas from Stromboli Volcano, Italy

We report the occurrence of unusual, high-magnesium (Fo₉₆) olivinephenocrysts in a basaltic lava and an ejected lithic block fromthe Upper Vancori period (13 ka) and the recent activity (2002–2003)of Stromboli volcano, Italy. The samples that contain this distinctivemineral chemistry are a shoshonitic basalt and a basaltic andesitewith anomalous bulk-rock chemical characteristics in which theiron is highly oxidized (6–8 wt % Fe₂O₃ and <1 wt %FeO). In other respects these samples are similar to the majorityof Stromboli basalts, characterized by the coexistence of olivine,clinopyroxene, plagioclase and Fe–Ti oxides as phenocrysts,and clinopyroxene, plagioclase and Fe–Ti oxides in thegroundmass. In the high-magnesium olivine samples, Fe–Tioxides (pseudobrookite) typically occur as symplectitic intergrowthswith the olivine phenocrysts, indicating simultaneous growthof the two phases. We propose, as a paragenetic model, thatthe Fo₉₆ olivine phenocrysts crystallized from a highly oxidizedbasaltic magma in which most of the iron was in the ferric state;hence, only magnesium was available to form olivine. The highlyoxidized state of the magma reflects sudden degassing of volatilephases associated with instantaneous, irreversible, transientdegassing of the magma chamber; this is postulated to occurduring periods of sudden decompression induced by fracturingof the volcanic edifice associated with paroxysmic activityand edifice collapse. KEY WORDS: Stromboli; Mg-rich olivine; oxygen fugacity; redox state of magmas; irreversible processes