Groundmass pargasite in the 1991–1995 dacite of Unzen volcano: phase stability experiments and volcanological implications

Pargasite commonly occurs in the dacitic groundmass of the 1991–1995 eruption products of Unzen volcano. We described the occurrence and chemical compositions of amphibole in the dacite, and also carried out melting experiments to determine the low-pressure stability limit of amphibole in the dacite. The 1991–1995 ejecta of the Unzen volcano show petrographic evidence of magma mixing, such as reverse compositional zoning of plagioclase and amphibole phenocrysts, and we used a groundmass separate as a starting material for the experiments. Reversed experiments show that the maximum temperature for the crystallization of amphibole is 930°C at 196 MPa, 900°C at 98 MPa, and 820°C at 49 MPa. Compared with the experimental results on the Mount St. Helens dacite, present experiments on the Unzen dacitic groundmass show that amphibole is stable to pressures ca. 50 MPa lower at 850°C. Available Fe–Ti oxide thermometry indicates the crystallization temperature of the groundmass of the Unzen dacite to be 880±30°C, suggesting that the groundmass pargasite crystallized at >70 MPa, corresponding to a depth of more than 3 km in the conduit. The chlorine content of the groundmass pargasite is much lower than that of phenocrystic magnesiohornblende in the 1991–1995 dacite of Unzen volcano, indicating that vesiculation/degassing of magma took place before the crystallization of the groundmass pargasite. The present study shows that the magma was water oversaturated and that the degassing of magma along with magma mixing caused crystallization of the groundmass amphibole at depths of more than 3 km in the conduit.     

Evidence for magma hybridization for the voluminous 29.5 Ma Wah Wah Springs Formation, Utah and Nevada, U.S.A.

The 29.5 Ma Wah Wah Springs Formation which erupted from the Indian Peak Caldera has an estimated volume of > 3900 km³ making it one of the largest ignimbrites on earth. The magma was calc-alkaline, dacitic (68 wt. % SiO₂) and phenocryst-rich (38 vol.%). Phenocrysts include plagioclase (An 47), magnesio-hornblende, Mg-biotite, quartz, Fe-Ti oxides, diopsidic-augite, and rare Ca-poor pyroxene, in order of decreasing abundance. Apatite, zircon and pyrrhotite occurs as inclusions within phenocrysts. Atmospheric glass losses (1040 km³) account for bulk-rock compositions that have SiO₂ contents ranging from 63 to 67 wt.%. Glass compositions are high-silica rhyolite.Phenocrysts equilibrated at temperatures ranging from about 790 to 850°C and oxygen fugacities approximately 2.6 log units above the QFM buffer. Confining pressure estimates using the aluminum-in-hornblende geobarometer calibrated for calc-alkaline volcanic rocks suggest a mean pressure of 230±50 MPa corresponding to 7.5±1.5 km depth. These estimates are consistent with caldera formation accompanying emplacement.Crystal compositions for phenocrysts and mineral inclusions within phenocrysts are remarkably homogeneous throughout the outflow tuff, although minor zoning does occur. Given the dacitic composition of the magma, the weakly zoned phenocryst population cannot be modeled to produce the observed high-silica glass (melt) indicating open-system behavior for the magma. The high-silica rhyolite glass is interpreted to be an artifact of efficient magma mixing accompanying addition of highly evolved magma, or melt to intermediate composition magma. Mixing was followed by magma hybridization. Additional support for this hybridization model includes: (1) physically and chemically distinct populations of augite; (2) minor but unbiquitous resorbed plagioclase, biotite and hornblende phenocrysts; and (3) reverse zoning in some of the plagioclase euhedra within pumice lapilli.     

The petrology and geochemistry of the Handkerchief Mesa mixed magma complex, San Juan Mountains, Colorado

The Handkerchief Mesa mixed magma complex is one of several late Cenozoic volcanic complexes in the southeastern San Juan Mountains characterized by mingling and limited mixing of basalt and rhyodacite. Stratigraphy in the dissected vent complex at Handkerchief Mesa records three phases of volcanism, the first and third displaying evidence for coeruption of mafic and silicic magmas. Phases 1 and 2 erupted silicic pyroclastics and basaltic lava flows, respectively. Phase-3 eruptions were dominated by rhyodacite lava flows, rhyodacite dikes, and abundant mingled and mixed hybrid lavas.Pre- and syneruptive basalt-rhyodacite mixing of phase-3 eruptions is shown by: (1) inclusions of quenched basalt in rhyodacite; (2) partially disaggregated basalt inclusions in mixed hybrids and rhyodacites; (3) interfingering lenses of mixed hybrid lavas and rhyodacite. Whole-rock major- and trace-element analyses support a two-component mixing model whereby intermediate hybrids are produced by mixing of basalt and rhyodacite (up to 30% basalt: 70% rhyodacite). Disequilibrium phenocryst textures and mineral compositions are consistent with multistage mixing culminating in an eruptive mixing event. Protracted mixing along a boundary zone at the base of a rhyodacite magma chamber may be responsible for stabilizing Fe-rich olivine phenocrysts in some hybrids.Basalt-rhyodacite mixing is inhibited by rapid crystallization in the basalt shortly after inclusion within the lower temperature melt. The degree to which mechanical dispersion and blending ensues is a critical function of the initial temperature contrast (ΔT_i) between the two magmas. Thermal models, simulating the conductive cooling histories for basalt spheres in rhyodacite reservoirs, suggest that at large ΔT_i's (> 200°) rapid cooling of the inclusion leads to disequilibrium crystallization with concomitant depression of equilibrium solidi, grain boundary wetting by residual liquids, and limited disaggregation of the inclusion imposed by movement of the host. For small ΔT_i's (< 100°) temperatures within the inclusion can be maintained above the solidus for prolonged time periods, enhancing the possibility of producing homogeneous mixed hybrids through mechanical blending and diffusion. Both mechanisms operated at Handkerchief Mesa and contributed to the range of observed textures and compositions.     

The Sr, Nd and O isotopic studies of the 1991–1995 eruption at Unzen, Japan

The magma generation at Unzen volcano may be considered as the product of crustal material mixed with mantle magma accompanied by fractional crystallization (AFC). The magma in the Unzen volcano is estimated to consist of about 50–80% of residual magma (F) and about 30–70% assimilated crustal material (A) relative to the original magma. Concerning the 1991–1995 eruption, it is estimated that the magma formed as the result of mixing of about 50–60% crustal material and about 55–65% of residual magma. An alternative magma eruption model for the 1991–1995 eruption is proposed here. In the early stage, the isotopic characteristics of 1991 eruption are defined by AFC process in the deeper magma chamber. Later, the magma ascended through the conduit and quiescently stayed for a long time in a shallow reservoir before eruption. The minerals continuously crystallized as phenocrysts especially at the chilled top and outer margin in the shallow chamber. The crystallized phenocryst mush was reworked into the central part of the magma chamber by means of magma convection and rapid magma ascent. Therefore, the reaction between phenocrysts and melt occurs only in internal chemical disequilibrium in the magma chamber. In contrast, the isotopic compositions of the original magma shall be little influenced by the above processes throughout its eruptive history. The 1991–1995 eruptive rocks of the Unzen volcano show their characteristics in Sr and Nd isotopic values independent of their two previous eruptions. However, the isotopic values of early eruptive product could represent the original magma value. This result also supports the previous work of Chen et al. (1993) [Chen, C.H., DePaolo, D.J., Nakada, S., Shieh, Y.N., 1993. Relationship between eruption volume and neodymium isotopic composition at Unzen volcano. Nature 362, 831–834], that suggested the Nd of early or precursory eruptive products could be a qualitative indicator of the maximum size of a continuing or impending eruption.     

Magma batches in the Timber Mountain magmatic system, Southwestern Nevada Volcanic Field, Nevada, USA

The common occurrence of compositionally and mineralogically zoned ash flow sheets, such as those of the Timber Mountain Group, provides evidence that the source magma bodies were chemically and thermally zoned. The Rainier Mesa and Ammonia Tanks tuffs of the Timber Mountain Group are both large volume (1200 and 900 km³, respectively) chemically zoned (57–78 wt.% SiO₂) ash flow sheets. Evidence of distinct magma batches in the Timber Mountain system are based on: (1) major- and trace-element variations of whole pumice fragments; (2) major-element variations in phenocrysts; (3) major-element variations in glass matrix; and (4) emplacement temperatures calculated from Fe-Ti oxides and feldspars. There are three distinct groups of pumice fragments in the Rainier Mesa Tuff: a low-silica group and two high-silica groups (a low-Th and a high-Th group). These groups cannot be related by crystal fractionation. The low-silica portion of the Rainier Mesa Tuff is distinct from the low-silica portion of the overlying Ammonia Tanks Tuff, even though the age difference is less than 200,000 years. Three distinct groups occur in the Ammonia Tanks Tuff: a low-silica, intermediate-silica and a high-silica group. Part of the high-silica group may be due to mixing of the two high-silica Rainier Mesa groups. The intermediate-silica group may be due to mixing of the low- and high-silica Ammonia Tanks groups. Three distinct emplacement temperatures occur in the Rainier Mesa Tuff (869, 804, 723 °C) that correspond to the low-silica, high-Th and low-Th magma batches, respectively. These temperature differences could not have been maintained for any length of time in the magma chamber (cf. Turner, J.S., Campbell, I.H., 1986. Convection and mixing in magma chambers. Earth-Sci. Rev. 23, 255–352; Martin, D., Griffiths, R.W., Campbell, I.H., 1987. Compositional and thermal convection in magma chambers. Contrib. Mineral. Petrol. 96, 465–475) and therefore eruption must have occurred soon after emplacement of the magma batches into the chamber. Emplacement temperatures of the pumice fragments from the Ammonia Tanks Tuff show a continuous gradient of temperatures with composition. This continuous temperature gradient is consistent with the model of storage of magma batches in the Ammonia Tanks group that have undergone both thermal and chemical diffusion.     

The Oligocene Lund Tuff, Great Basin, USA: a very large volume monotonous intermediate

Unusual monotonous intermediate ignimbrites consist of phenocryst-rich dacite that occurs as very large volume (>1000 km³) deposits that lack systematic compositional zonation, comagmatic rhyolite precursors, and underlying plinian beds. They are distinct from countless, usually smaller volume, zoned rhyolite–dacite–andesite deposits that are conventionally believed to have erupted from magma chambers in which thermal and compositional gradients were established because of sidewall crystallization and associated convective fractionation. Despite their great volume, or because of it, monotonous intermediates have received little attention. Documentation of the stratigraphy, composition, and geologic setting of the Lund Tuff – one of four monotonous intermediate tuffs in the middle-Tertiary Great Basin ignimbrite province – provides insight into its unusual origin and, by implication, the origin of other similar monotonous intermediates.The Lund Tuff is a single cooling unit with normal magnetic polarity whose volume likely exceeded 3000 km³. It was emplaced 29.02±0.04 Ma in and around the coeval White Rock caldera which has an unextended north–south diameter of about 50 km. The tuff is monotonous in that its phenocryst assemblage is virtually uniform throughout the deposit: plagioclase>quartz≈hornblende>biotite>Fe–Ti oxides≈sanidine>titanite, zircon, and apatite. However, ratios of phenocrysts vary by as much as an order of magnitude in a manner consistent with progressive crystallization in the pre-eruption chamber. A significant range in whole-rock chemical composition (e.g., 63–71 wt% SiO₂) is poorly correlated with phenocryst abundance.These compositional attributes cannot have been caused wholly by winnowing of glass from phenocrysts during eruption, as has been suggested for the monotonous intermediate Fish Canyon Tuff. Pumice fragments are also crystal-rich, and chemically and mineralogically indistinguishable from bulk tuff. We postulate that convective mixing in a sill-like magma chamber precluded development of a zoned chamber with a rhyolitic top or of a zoned pyroclastic deposit. Chemical variations in the Lund Tuff are consistent with equilibrium crystallization of a parental dacitic magma followed by eruptive mixing of compositionally diverse crystals and high-silica rhyolite vitroclasts during evacuation and emplacement. This model contrasts with the more systematic withdrawal from a bottle-shaped chamber in which sidewall crystallization creates a marked vertical compositional gradient and a substantial volume of capping-evolved rhyolite magma. Eruption at exceptionally high discharge rates precluded development of an underlying plinian deposit.The generation of the monotonous intermediate Lund magma and others like it in the middle Tertiary of the western USA reflects an unusually high flux of mantle-derived mafic magma into unusually thick and warm crust above a subducting slab of oceanic lithosphere.     

Pre-eruptive and syn-eruptive conditions in the Black Butte, California dacite: Insight into crystallization kinetics in a silicic magma system

A series of experiments and petrographic analyses have been run to determine the pre-eruption phase equilibria and ascent dynamics of dacitic lavas composing Black Butte, a dome complex on the flank of Mount Shasta, California. Major and trace element analyses indicate that the Black Butte magma shared a common parent with contemporaneously erupted magmas at the Shasta summit. The Black Butte lava phenocryst phase assemblage (20 v.%) consists of amphibole, plagioclase (core An_77.5), and Fe–Ti oxides in a fine-grained (< 0.5 mm) groundmass of plagioclase, pyroxene, Fe–Ti oxides, amphibole, and cristobalite. The phenocryst assemblage and crystal compositions are reproduced experimentally between 890 °C and 910 °C, ≥ 300 MPa, X_H2O = 1, and oxygen fugacity = NNO + 1. This study has quantified the extent of three crystallization processes occurring in the Black Butte dacite that can be used to discern ascent processes. Magma ascent rate was quantified using the widths of amphibole breakdown rims in natural samples, using an experimental calibration of rim development in a similar magma at relevant conditions. The majority of rims are 34 ± 10 μm thick, suggesting a time-integrated magma ascent rate of 0.004–0.006 m/s among all four dome lobes. This is comparable to values for effusive samples from the 1980 Mount St. Helens eruption and slightly faster than those estimated at Montserrat. A gap between the compositions of plagioclase phenocryst cores and microlites suggests that while phenocryst growth was continuous throughout ascent, microlite formation did not occur until significantly into ascent. The duration of crystallization is estimated using the magma reservoir depth and ascent rate, as determined from phase equilibria and amphibole rim widths, respectively. Textural analysis of the natural plagioclase crystals yields maximum growth rates of plagioclase phenocryst rims and groundmass microlites of 8.7 × 10^− 8 and 2.5 × 10^− 8 mm/s, respectively. These rates are comparable to values determined from time-sequenced samples of dacite erupted effusively from Mount St. Helens during 1980 and indicate that syneruptive crystallization processes were important during the Black Butte eruptive cycle.     

Mineralogical and geochemical evolution of the 1982–1983 Galunggung eruption (Indonesia)

Pyroclastic deposits from the 1982–1983 eruption of Galunggung volcano (Java, Indonesia) reflect preeruptive magmatic evolution which is of interest because of: (1) its duration of nine months, compared to a few hours or days for most historical eruptions; (2) the diversity of eruptive styles, from ash and scoria flows to phreatomagmatic explosions, and to the strombolian activity that marked the end of the eruption; and (3) the progressive variation in chemical composition with time, from andesite (58 wt.% SiO₂) to high-Mg basalt (47 wt.% SiO₂). The 1982–1983 Galunggung basalts are rather primitive: 10 to 12 wt% MgO, 180 to 200 ppm Ni and 550 to 700 ppm Cr. Despite the presence of about 40% phenocrysts, they may represent the most primitive basalts recognized in western Java. Basalts contain phenocrysts of olivine (Fo_90-80), diopside-salite, and plagioclase (An_95-75). Andesites contain plagioclase (An_80–60), augite, hypersthene (En_67-64), and titanomagnetite. The distribution of mineral compositions in each petrographic type is nearly unimodal, although scarce plagioclase and olivine xenocrysts have been observed. Abundance of gabbroic cumulates associated with the pyroclastic flows and evolution of mineral compositions from high-Mg basalts to andesites support crystal fractionation as the main differentiation mechanism, although magma mixing of basaltic andesite and andesite cannot be excluded. Major and trace element trends, which display rough decreases of MgO, CaO, Ni, Cr with increasing degree of differentiation and also linear positive correlations of hygromagmaphile elements, are compatible with both processes. However, some discrepancies are observed between major and trace element modelling, which may be explained to some extent by the influence of in situ crystallization and/or magma mixing. The constancy of ¹⁴³Nd/¹⁴⁴Nd (0.51286±3), ²³⁰Th/²³²Th (0.65±0.02), Th/U (4.08±0.07) ratios, and to a lesser extent ¹⁸O values (+5.8 to +6.4 % SMOW) and ⁸⁷Sr/⁸⁶Sr ratios (0.70440 to 0.70468) is compatible with a magmatic evolution through fractional crystallization without significant crustal contamination. Nevertheless low-¹⁸O and high ⁸⁷Sr/⁸⁶Sr values in basaltic andesites may be due to the introduction of meteoric fluids into the Galunggung magma.     

Comparative temperature measurements on mount etna lavas: problems and techniques

On the basis of investigations carried out since 1966 at Mount Etna, the temperatures of erupting magmas are shown to be determined within a few °C in the range 1000–1200°C, by using suitable techniques and apparatus. The best measurements are obtained from sheathed thermocouples that are briefly described. Particularly, a new continuously recording multithermocouple system has been designed, tested satisfactorily, and compared with the performances of other pyrometers. However, a certain standardization of measurements is necessary to obtain and discuss the results: measurements should be made at lava vents or a few meters away and at least 30–50 cm into the flows, the highest values only being considered as significant.The magmatic temperatures and petrological characters appear closely related to the volcanic activity. In the normal state of moderate persistent activity of Mount Etna, the alkaline basic magma extrudes at a nearly constant temperature of 1080°C (corresponding to about 50% crystalline phases), meanwhile during stronger paroxysmal eruptions the magma temperature is higher (1125°C and possibly more) with a lower observed content of phenocrysts.     

Melt inclusion analysis of the Unzen 1991–1995 dacite: implications for crystallization processes of dacite magma

Dacitic magma, a mixture of high-temperature (T) aphyric magma and low-T crystal-rich magma, was erupted during the 1991–1995 Mount Unzen eruptive cycle. Here, the crystallization processes of the low-T magma were examined on the basis of melt inclusion analysis and phase relationships. Variation in water content of the melt inclusions (5.1–7.2 wt% H₂O) reflected the degassing history of the low-T magma ascending from deeper levels (250 MPa) to a shallow magma chamber (140 MPa). The ascent rate of the low-T magma decreased markedly towards the emplacement level as crystal content increased. Cooling of magma as well as degassing-induced undercooling drove crystallization. With the decreasing ascent rate, degassing-induced undercooling decreased in importance, and cooling became more instrumental in crystallization, causing local and rapid crystallization along the margin of the magma body. Some crystals contain scores of melt inclusions, whereas there are some crystals without any inclusions. This heterogeneous distribution suggests the variation in the crystallization rate within the magma body; it also suggests that cooling was dominant cause for melt entrapment. Numerical calculations of the cooling magma body suggest that cooling caused rapid crystal growth and enhanced melt entrapment once the magma became a crystal-rich mush with evolved interstitial melt. The rhyolitic composition of melt inclusions is consistent with this model.Editorial responsibility: H Shinohara     

Magma plumbing system of the 2000 eruption of Miyakejima Volcano, Japan

During the 2000 eruption at Miyakejima Volcano, two magmas with different compositions erupted successively from different craters. Magma erupted as spatter from the submarine craters on 27 June is aphyric basaltic andesite (<5 vol% phenocrysts, 51.4–52.2 wt% SiO₂), whereas magma issued as volcanic bombs from the summit caldera on 18 August is plagioclase-phyric basalt (20 vol% phenocrysts, 50.8–51.3 wt% SiO₂). The submarine spatter contains two types of crystal-clots, A-type and A-type (andesitic type). The phenocryst assemblages (plagioclase, pyroxenes and magnetite) and compositions of clinopyroxene in these clots are nearly the same, but only A-type clots contain Ca-poor plagioclase (An < 70). We consider that the A-type clots could have crystallized from a more differentiated andesitic magma than the A-type clots, because FeO*/MgO is not strongly influenced during shallow andesitic differentiation. The summit bombs contain only B-type (basaltic type) crystal-clots of Ca-rich plagioclase, olivine and clinopyroxene. The A-type and B-type clots have often coexisted in Miyakejima lavas of the period 1469–1983, suggesting that the magma storage system consists of independent batches of andesitic and basaltic magmas. According to the temporal variations of mineral compositions in crystal-clots, the andesitic magma became less evolved, and the basaltic magma more evolved, over the past 500 years. We conclude that gradually differentiating basaltic magma has been repeatedly injected into the shallower andesitic magma over this period, causing the andesitic magma to become less evolved with time. The mineral chemistries in crystal-clots of the submarine spatter and 18 August summit bombs of the 2000 eruption fall on the evolution trends of the A-type and B-type clots respectively, suggesting that the shallow andesitic and deeper basaltic magmas existing since 1469 had successively erupted from different craters. The 2000 summit collapse occurred due to drainage of the andesitic magma from the shallower chamber; as the collapse occurred, it may have caused disruption of crustal cumulates which then contaminated the ascending, deeper basalt. Thus, porphyritic basaltic magma could erupt alone without mixing with the andesitic magma from the summit caldera. The historical magma plumbing system of Miyakejima was probably destroyed during the 2000 eruption, and a new one may now form.Editorial responsibility: S Nakada, T Druitt     

The magmatic feeding system of El Reventador volcano (Sub-Andean zone,Ecuador) constrained by texture,mineralogy and thermobarometry of the 2002 erupted products

After a 26 years long quiescence El Reventador, an active volcano of the rear-arc zone of Ecuador, entered a new eruptive cycle which lasted from 3 November to mid December 2002. The initial sub-Plinian activity (VEI 4 with andesite pyroclastic falls and flows) shifted on 6 and 21 November to an effusive stage characterized by the emission of two lava flows (andesite to low-silica andesite Lava-1 and basaltic andesite Lava-2) containing abundant gabbro cumulates. The erupted products are medium to high-K calc-alkaline and were investigated with respect to major element oxides, mineral chemistry, texture and thermobarometry. Inferred pre-eruptive magmatic processes are dominated by the intrusion of a high-T mafic magma (possibly up to 1165 ± 15 °C) into an andesite reservoir, acting as magma mixing and trigger for the eruption. Before this refilling, the andesite magma chamber was characterized by water content of 5.3 ± 1.0%, high oxygen fugacity (> NNO + 2) and temperatures, in the upper and lower part of the reservoir, of 850 and 952 ± 65 °C respectively. Accurate amphibole-based barometry constrains the magma chamber depth between 8.2 and 11.3 km (± 2.2 km). The 6 October 2002 seismic swarm (hypocenters from 10 to 11 km) preceding El Reventador eruption, supports the intrusion of magmas at these depths. The widespread occurrence of disequilibrium features in most of the andesites (e.g. complex mineral zoning and phase overgrowths) indicates that convective self-mixing have been operating together with fractional crystallization (inferred from the cognate gabbro cumulates) before the injection of the basic magma which then gave rise to basaltic andesite and low-silica andesite hybrid layers. Magma mixing in the shallow chamber is inferred from the anomalous SiO₂–Al₂O₃ whole-rock pattern and strong olivine disequilibria. Both lavas show three types of amphibole breakdown rims mainly due to heating (mixing processes) and/or relatively slow syn-eruptive ascent rate (decompression) of the magmas. The lack of any disequilibrium textures in the pumices of the 3 November fall deposit suggest that pre-eruptive mixing did not occur in the roof zone of the chamber. A model of the subvolcanic feeding system of El Reventador, consistent with the intrusion of a low-Al₂O₃ crystal-rich basic magma into an already self-mixed andesite shallow reservoir, is here proposed. It is also inferred that before entering the shallow chamber the “basaltic” magma underwent a polybaric crystallization at deeper crustal levels.     

Effusive eruption of viscous silicic magma triggered and driven by recharge: a case study of the Cerro Chascon-Runtu Jarita Dome Complex in Southwest Bolivia

 The Cerro Chascon-Runtu Jarita Complex is a group of ten Late Pleistocene (∼85 ka) lava domes located in the Andean Central Volcanic Zone of Bolivia. These domes display considerable macroscopic and microscopic evidence of magma mixing. Two groups of domes are defined chemically and geographically. A northern group, the Chascon, consists of four lava bodies of dominantly rhyodacite composition. These bodies contain 43–48% phenocrysts of plagioclase, quartz, sanidine, biotite, and amphibole in a microlite-poor, rhyolitic glass. Rare mafic enclaves and selvages are present. Mineral equilibria yield temperatures from 640 to 750  °C and log ƒO₂ of –16. Geochemical data indicate that the pre-eruption magma chamber was zoned from a dominant volume of 68% to minor amounts of 76% SiO₂. This zonation is best explained by fractional crystallization and some mixing between rhyodacite and more evolved compositions. The mafic enclaves represent magma that intruded but did not chemically interact much with the evolved magmas. A southern group, the Runtu Jarita, is a linear chain of six small domes (<1 km³ total volume) that probably is the surface expression of a dike. The five most northerly domes are composites of dacitic and rhyolitic compositions. The southernmost dome is dominantly rhyolite with rare mafic enclaves. The composite domes have lower flanks of porphyritic dacite with ∼35 vol.% phenocrysts of plagioclase, orthopyroxene, and hornblende in a microlite-rich, rhyodacitic glass. Sieve-textured plagioclase, mixed populations of disequilibrium plagioclase compositions, xenocrystic quartz, and sanidine with ternary composition reaction rims indicate that the dacite is a hybrid. The central cores of the composite domes are rhyolitic and contain up to 48 vol.% phenocrysts of plagioclase, quartz, sanidine, biotite, and amphibole. This is separated from the dacitic flanks by a banded zone of mingled lava. Macroscopic, microscopic, and petrologic evidence suggest scavenging of phenocrysts from the silicic lava. Mineral equilibria yield temperatures of 625–727  °C and log ƒO₂ of –16 for the rhyolite and 926–1000  °C and log ƒO₂ of –9.5 for the dacite. The rhyolite is zoned from 73 to 76% SiO₂, and fractionation within the rhyolite composition produced this variation. Most of the 63–73% SiO₂ compositional range of the lava in this group is the result of mixing between the hybrid dacite and the rhyolite. Eruption of both groups of lavas apparently was triggered by mafic recharge. A paucity of explosive activity suggests that volatile and thermal exchanges between reservoir and recharge magmas were less important than volume increase and the lubricating effects of recharge by mafic magmas. For the Runtu Jarita group, the eruption is best explained by intrusion of a dike of dacite into a chamber of crystal-rich rhyolite close to its solidus. The rhyolite was encapsulated and transported to the surface by the less-viscous dacite magma, which also acted as a lubricant. Simultaneous effusion of the lavas produced the composite domes, and their zonation reflects the subsurface zonation. The role of recharge by hotter, more fluid mafic magma appears to be critical to the eruption of some highly viscous silicic magmas. Received: 23 August 1998 / Accepted: 10 March 1999     

Hawaiian magma-reservoir processes as inferred from the petrology of gabbro xenoliths in basalt,Kahoolawe Island

Gabbro xenoliths in a tholeiitic lava of Kahoolawe Island, Hawaii, a 1.3–1.4 Ma shield volcano, are 1–3 cm in size and comprised of plagioclase, clinopyroxene, and orthopyroxene. Gabbro textures — while intergranular and in part subophitic-are open due to 28–48 vol.% of vesicular basalt occupying xenolith space. Vesicles in and around the xenoliths are lined or filled with rhyolitic glass (segregation vesicles). The host is evolved tholeiite (MgO 6.1 wt%) with phenocrysts, microphenocrysts, and glomerocrysts of olivine, clinopyroxene, orthopyroxene, and plagioclase, and megacrysts (1 cm) of plagioclase. The Sr-isotope ratio of one xenolith is 0.70489; the host basalt ratio is 0.70460. Xenolith isotope composition, grain resorption, and clinopyroxene (Fs_12.5–15Wo_38–35.5), orthopyroxene (Fs_19.5–24Wo_4.1), and plagioclase (An_68–65Or_0.8–1.2) compositions suggest that these gabbros crystallized from Kahoolawe tholeiitic magma of essentially the same composition as the host basalt, but pre-dating the magma represented by the host. Based on the absence of intergranular Fe–Ti oxide phases from the pl+cpx+opx assemblages, and the open, vuggy textures, we envision crystallization on a reservoir roof at temperatures >1100°C. Entrainment of gabbro assemblages and plagioclase megacrysts from a roof mush/suspension zone occurred during convection associated with replenishment of the magma reservoir. These open-textured gabbro xenoliths are therefore not fragments of preexisting coarse-grained bodies such as sills or segregation veins. Rhyolitic glass in vesicles represents a gas-effervescence filtration process that forced fractionated residual liquids from the groundmass into voids associated with the xenoliths.Sirrine Environmental Consultants, Fremont, CA 94538     

Role of precursory less-viscous mixed magma in the eruption of phenocryst-rich magma: evidence from the Hokkaido-Komagatake 1929 eruption

During the 1929 activity of Hokkaido-Komagatake volcano, the Plinian eruption of a phenocryst-rich andesite was preceded by a small eruption of more mafic magma formed by magma mixing. A similar eruption sequence has been reported for some other eruptions (Pallister et al. 1996; Venezky and Rutherford 1997), suggesting that eruption of a mixed magma is a precursor of phenocryst-rich magmas. For the purpose of understanding the tapping processes of the phenocryst-rich magma chamber, we investigated the temporal variation in the erupted magma and estimated the viscosity and density of the end-member and mixed magmas with constraints drawn from petrography. For the precursory mixed magma we estimate 33dž vol.% phenocrysts, andesitic-dacitic melt composition, 3 wt.% H₂O content, and temperature of 1040°C. In comparison, for the climactic, silicic end-member magma we estimate 48Dž vol.% phenocryst, high-silica rhyolitic melt, 3 wt.% H₂O, and temperature of 950°C, respectively. The mafic end-member magma, which was not erupted, is thought to be an almost aphyric basaltic-andesitic magma, based on mass balance calculation of the phenocryst content. The proportion of the mafic end-member magma component in the mixed magma was calculated to be 20-40 wt.%. On the basis of these data, we estimate magma viscosities of 10^3.9, 10^6.9, and 10^2.0 Pa s for the mixed, silicic end-member, and mafic end-member magmas, respectively. The calculated density differences among these magmas are inconsequential when possible errors are considered. We calculate the minimum excess pressure required for dike propagation to be 31 MPa for the silicic end-member magma and 8 MPa for the mixed magma, using the estimated viscosity and dike propagation model of Rubin (1995). If we assume that excess pressure is limited by the wall rock strength of the magma chamber, excess pressure retainable in the magma chamber is less than ca. 20 MPa. This suggests that the mixed magma was able to ascend to the surface without freezing, whereas the viscous silicic end-member magma could not. The formation and precursory eruption of the mixed magma are, therefore, effective and necessary initiation processes for the phenocryst-rich, viscous magma eruption.     

Genesis of high-magnesium andesites and associated basalts from Saga–Futagoyama, northwest Kyushu, southwest Japan

High-magnesium andesites associated with basalts erupted after the opening of the Sea of Japan are present at Saga–Futagoyama in northwest Kyushu, southwest Japan. High Mg/(Mg + Fe) [=0.84] of orthopyroxene phenocrysts and bulk rock Mg–Fe–Ni compositions suggest that these high-magnesium andesites were originally primitive melts insignificantly modified in crustal magma chambers. K_D^Ca–Na [= (Ca/Na)_pl/(Ca/Na)_{bulk rock}] ranges from 1.21 to 0.97 and suggests that the high-magnesium andesite magmas would originally have contained H₂O less than 1.8 wt.%. Nb/La does not show a negative correlation with respect to SiO₂. These lines of evidence indicate that hydrous components derived from the subducting slab would not have played a significant role in the genesis of the high-magnesium andesite magmas. Instead, the normative olivine − quartz − [CaTs + Jd] compositions and a negative correlation between Sr/Nd and SiO₂ indicate that the basalt-high-magnesium andesite association would have been formed by multi-stage partial melting of relatively anhydrous source at pressure ranging from 1.5 to 0.5 GPa.     

Differentiation and magma mixing on Kilauea's east rift zone

The lavas of the 1955 east rift eruption of Kilauea Volcano have been the object of considerable petrologic interest for two reasons. First, the early 1955 lavas are among the most differentiated ever erupted at Kilauea, and second, the petrographic character and chemical composition of the lava being erupted changed significantly during the eruption. This shift, from more differentiated (MgO=5.0–5.7%) to more magnesian (MgO=6.2–6.8%) lava, has been variously interpreted, as either due to systematic excavation of a zoned, differentiated magma body, or to invasion of the differentiated magma by more primitive magma, followed by rapid mixing and eruption of the resulting hybrid magmas. Petrologic examination of several nearvent spatter samples of the late 1955 lavas shows abundant evidence for magma mixing, including resorbed and/or reversely zoned crystals of olivine, augite and plagioclase. In addition, the compositional ranges of olivine, plagioclase and groundmass sulfide are very large, implying that the assemblages are hybrid. Core compositions of olivine phenocrysts range from Fo85 to Fo77. The most magnesian olivines in these samples must have originally crystallized from a melt containing 8.0–8.5% MgO, which is distinctly more magnesian than the bulk composition of the late 1955 lavas. The majorelement and trace-element data are either permissive or supportive of a hybrid origin for the late 1955 lavas. In particular, the compositional trends of the 1955 lavas on plots of CaO vs MgO, and the virtual invariance of Al₂O₃ and Sr in these plagioclase-phyric lavas are more easily explained by magma mixing than by fractionation. The pattern of internal disequilibrium/re-equilibration in the late 1955 spatter samples is consistent with reintrusion and mixing having occurred at least twice, during the latter part of the 1955 eruption. Plagioclase zonation preserves possible evidence for additional, earlier reintrusion events. Least-squares modelling the mixing of early 1955 bulk compositions with various summit lavas±olivine pick the 1952 summit lava as most like the primitive component. The results also indicate the primitive component had MgO=7.5–8.0%, corresponding to liquidus temperatures of 1165–1175°C. The absence of Fe-Ti oxide phenocrysts in the late 1955 lavas implies that the cooler component of the hybrid had T>1110°C. Thus the thermal contrast between the two components may have been as much as 55–65°C, sufficient to produce the conspicuous disequilibrium effects visible in the spatter samples.     

Heterogeneous pumice populations in the 2.08-Ma Cerro Gal��n Ignimbrite: implications for magma recharge and ascent preceding a large-volume silicic eruption

Triggering mechanisms of large silicic eruptions remain a critical unsolved problem. We address this question for the ~2.08-Ma caldera-forming eruption of Cerro Galán volcano, Argentina, which produced distinct pumice populations of two colors: grey (5%) and white (95%) that we believe may hold clues to the onset of eruptive activity. We demonstrate that the color variations correspond to both textural and compositional variations between the clast types. Both pumice types have bulk compositions of high-K, high-silica dacite to low-silica rhyolite, but there are sufficient compositional differences (e.g., ~150?ppm lower Ba at equivalent SiO₂ content and 0.03?wt.% higher TiO₂ in white pumice than grey) to suggest that the two pumice populations are not related by simple fractionation. Trace element concentrations in crystals mimic bulk variations between clast types, with grey pumice containing elevated Ba, Cu, Pb, and Zn concentrations in both bulk samples (average Cu, Pb, and Zn concentrations are 27, 35, and 82 in grey pumice vs. 11, 19, and 60 in white pumice) and biotite phenocrysts and white pumice showing elevated Li concentrations in biotite and plagioclase phenocrysts. White and grey clasts are also texturally distinct: White pumice clasts contain abundant phenocrysts (44?C57%), lack microlites, and have highly evolved groundmass glass compositions (76.4?C79.6?wt.% SiO₂), whereas grey pumice clasts contain a lower percentage of phenocrysts/microphenocrysts (35?C49%), have abundant microlites, and have less evolved groundmass glass compositions (69.4?C73.8?wt.% SiO₂). There is also evidence for crystal transfer between magma producing white and grey pumice. Thin highly evolved melt rims surround some fragmental crystals in grey pumice clasts and appear to have come from magma that produced white pumice. Furthermore, based on crystal compositions, white bands within banded pumice contain crystals originating in grey magma. Finally, only grey pumice clasts form breadcrusted surface textures. We interpret these compositional and textural variations to indicate distinct magma batches, where grey pumice originated from an originally deeper, more volatile-rich dacite recharge magma that ascended through and mingled with the volumetrically dominant, more highly crystalline chamber that produced white pumice. Shortly before eruption, the grey pumice magma stalled within shallow fractures, forming a vanguard magma phase whose ascent may have provided a trigger for eruption of the highly crystalline rhyodacite magma. We suggest that in the case of the Cerro Galán eruption, grey pumice provides evidence not only for cryptic silicic recharge in a large caldera system but also a probable trigger for the eruption.     

Composite titanomagnetite-ferrian ilmenite grains and correlative magnetic components in a dacite with self-reversed TRM

Electron microprobe and reflected light microscopic examinations confirm the presence of composite grains of ferrian ilmenite with X_ilm = 0.53 and titanomagnetite with X_usp = 0.13 in a dacite with self-reversed TRM. A parallel TRM component associated with titanomagnetite and a reversed component associated with self-reversing ferrian ilmenite are the principal NRM components. A subordinate, parallel component is associated with ferrian ilmenite which is not magnetically coupled to an “χ-phase”. The natural self-reversing properties are mainly a consequence of the dacite's high quenching temperature, calculated at 862–864°C using the Fe—Ti oxide geothermometer, and are most consistent with the self-reversal mechanism proposed by Lawson et al. [9].The conduction of thermal demagnetization and TRM induction tests in air had a much greater effect on the Fe—Ti oxides than did natural cooling, and resulted in significant oxidation with the consequent modification of some magnetic properties and the formation of another reversed TRM component. The subdivision of titanomagnetite grains by oxidation along fractures decreased its effective grain size and caused an apparent increase in its magnetic intensity, in addition to a slight increase in its resistance to alternating field demagnetization. The χ-phase associated with the reversed NRM component, with 0.42 > X_ilm 0.31, became Fe-enriched during the earlier stages of heat treatment. It is suggested that after heating at 600°C for two hours or more, this χ-phase exsolves as titanohematite with X_ilm < 0.33. The ferrian ilmenite host is consequently enriched in Ti, and another χ-phase much closer in composition to the host generates a reversed TRM component with T_b < 200°C.     

Chemical geothermometry and fluid–mineral equilibria for the Ömer–Gecek thermal waters, Afyon area, Turkey

Thermal waters of the Ömer–Gecek geothermal field, Turkey, with temperatures ranging from 32 to 92°C vary in chemical composition and TDS contents. They are generally enriched in Na–Cl–HCO₃ and suggest deep water circulation. Silica and cation geothermometers applied to the Ömer–Gecek thermal waters yield reservoir temperatures of 75–155°C. The enthalpy–chloride mixing model, which approximates a reservoir temperature of 125°C for the Ömer–Gecek field, accounts for the diversity in the chemical composition and temperature of the waters by a combination of processes including boiling and conductive cooling of deep thermal water and mixing of the deep thermal water with cold water. It is also determined that the solubility of silica in most of the waters is controlled by the chalcedony phase. Equilibrium states of the Ömer–Gecek thermal waters studied by means of the Na–K–Mg triangular diagram, Na–K–Mg–Ca diagram, K–Mg–Ca geoindicator diagram, activity diagrams in the systems composed of Na₂O–CaO–K₂O–Al₂O₃–SiO₂–CO₂–H₂O phases, log SI diagrams, and finally the alteration mineralogy indicate that most of the spring and low-temperature well waters in the area can be classified as shallow or mixed waters which are likely to be equilibrated with calcite, chalcedony and kaolinite at predicted temperature ranges similar to those calculated from the chemical geothermometers. It was also observed that mineral equilibrium in the Ömer–Gecek waters is largely controlled by CO₂ concentrations.