Crystal fractionation,magma step ascent,and syn-eruptive mingling: the Averno 2 eruption (Phlegraean Fields,Italy)

The 3.7 ka year-old Averno 2 eruption is one of the rare eruptions to have occurred in the northwest sector of the Phlegraean Fields caldera (PFc) over the past 5 ka. We focus here on the fallout deposits of the pyroclastic succession emplaced during this eruption. We present major and trace element data on the bulk pumices, along with major and volatile element data on clinopyroxene-hosted melt inclusions, in order to assess the conditions of storage, ascent, and eruption of the feeding trachytic magma. Crystal fractionation accounts for the evolution from trachyte to alkali-trachyte magmas; these were intimately mingled (at the micrometer scale) during the climactic phase of the eruption. The Averno 2 alkali trachyte represents one of the most evolved magmas erupted within the Phlegraean Fields area and belongs to the series of differentiated trachytic magmas erupted at different locations 5 ka ago. Melt inclusions record significant variations in H₂O (from 0.4 to 5 wt%), S (from 0.01 to 0.06 wt%), Cl (from 0.75 up to 1 wt%), and F (from 0.20 to >0.50 wt%) during both magma crystallization and degassing. Unlike the eruptions occurring in the central part of the PFc, deep-derived input(s) of gas and/or magma are not required to explain the composition of melt inclusions and the mineralogy of Averno 2 pumices. Compositional data on bulk pumices, glassy matrices, and melt inclusions suggest that the Averno 2 eruption mainly resulted from successive extrusions of independent magma batches probably emplaced at depths of 2–4 km along regional fractures bordering the Neapolitan Yellow Tuff caldera.     

Geochemical and isotopic insights into the assembly,evolution and disruption of a magmatic plumbing system before and after a cataclysmic caldera-collapse eruption at Ischia volcano (Italy)

New geochemical and isotopic data on volcanic rocks spanning the period ~75–50 ka BP on Ischia volcano, Italy, shed light on the evolution of the magmatic system before and after the catastrophic, caldera-forming Monte Epomeo Green Tuff (MEGT) eruption. Volcanic activity during this period was influenced by a large, composite and differentiating magmatic system, replenished several times with isotopically distinct magmas of deep provenance. Chemical and isotopic variations highlight that the pre-MEGT eruptions were fed by trachytic/phonolitic magmas from an isotopically zoned reservoir that were poorly enriched in radiogenic Sr and became progressively less radiogenic with time. Just prior to the MEGT eruption, the magmatic system was recharged by an isotopically distinct magma, relatively more enriched in radiogenic Sr with respect to the previously erupted magmas. This second magma initially fed several SubPlinian explosive eruptions and later supplied the climactic, phonolitic-to-trachytic MEGT eruption(s). Isotopic data, together with erupted volume estimations obtained for MEGT eruption(s), indicate that >5–10 km³ of this relatively enriched magma had accumulated in the Ischia plumbing system. Geochemical modelling indicates that it accumulated at shallow depths (4–6 km), over a period of ca. 20 ka. After the MEGT eruption, volcanic activity was fed by a new batch of less differentiated (trachyte-latite) magma that was slightly less enriched in radiogenic Sr. The geochemical and Sr–Nd-isotopic variations through time reflect the upward flux of isotopically distinct magma batches, variably contaminated by Hercynian crust at 8–12 km depth. The deep-sourced latitic to trachytic magmas stalled at shallow depths (4–6 km depth), differentiated to phonolite through crystal fractionation and assimilation of a feldspar-rich mush, or ascended directly to the surface and erupted.     

Pre- and syn-eruptive degassing and crystallisation processes of the 2010 and 2006 eruptions of Merapi volcano,Indonesia

The 2010 eruption of Merapi (VEI 4) was the volcano’s largest since 1872. In contrast to the prolonged and effusive dome-forming eruptions typical of Merapi’s recent activity, the 2010 eruption began explosively, before a new dome was rapidly emplaced. This new dome was subsequently destroyed by explosions, generating pyroclastic density currents (PDCs), predominantly consisting of dark coloured, dense blocks of basaltic andesite dome lava. A shift towards open-vent conditions in the later stages of the eruption culminated in multiple explosions and the generation of PDCs with conspicuous grey scoria and white pumice clasts resulting from sub-plinian convective column collapse. This paper presents geochemical data for melt inclusions and their clinopyroxene hosts extracted from dense dome lava, grey scoria and white pumice generated during the peak of the 2010 eruption. These are compared with clinopyroxene-hosted melt inclusions from scoriaceous dome fragments from the prolonged dome-forming 2006 eruption, to elucidate any relationship between pre-eruptive degassing and crystallisation processes and eruptive style. Secondary ion mass spectrometry analysis of volatiles (H₂O, CO₂) and light lithophile elements (Li, B, Be) is augmented by electron microprobe analysis of major elements and volatiles (Cl, S, F) in melt inclusions and groundmass glass. Geobarometric analysis shows that the clinopyroxene phenocrysts crystallised at depths of up to 20 km, with the greatest calculated depths associated with phenocrysts from the white pumice. Based on their volatile contents, melt inclusions have re-equilibrated during shallower storage and/or ascent, at depths of ~0.6–9.7 km, where the Merapi magma system is interpreted to be highly interconnected and not formed of discrete magma reservoirs. Melt inclusions enriched in Li show uniform “buffered” Cl concentrations, indicating the presence of an exsolved brine phase. Boron-enriched inclusions also support the presence of a brine phase, which helped to stabilise B in the melt. Calculations based on S concentrations in melt inclusions and groundmass glass require a degassing melt volume of 0.36 km³ in order to produce the mass of SO₂ emitted during the 2010 eruption. This volume is approximately an order of magnitude higher than the erupted magma (DRE) volume. The transition between the contrasting eruptive styles in 2010 and 2006 is linked to changes in magmatic flux and changes in degassing style, with the explosive activity in 2010 driven by an influx of deep magma, which overwhelmed the shallower magma system and ascended rapidly, accompanied by closed-system degassing.     

Modeling the multi-level plumbing system of the Changbaishan caldera from geochemical,mineralogical, Sr-Nd isotopic and integrated geophysical data

Changbaishan, an intraplate volcano, is characterized by an approximately 6 km wide summit caldera and last erupted in 1903. Changbaishan experienced a period of unrest between 2002 and 2006. The activity developed in three main stages, including shield volcano(basalts), cone-construction(trachyandesites to trachytes with minor basalts), and caldera-forming stages(trachytes to comendites). This last stage is associated with one of the more energetic eruptions of the last millennium on Earth, the 946 CE, VEI 7 Millennium Eruption(ME),which emitted over 100 km3 of pyroclastics. Compared to other active calderas, the plumbing system of Changbaishan and its evolution mechanisms remain poorly constrained. Here, we merge new whole-rock,glass, mineral, isotopic, and geobarometry data with geophysical data and present a model of the plumbing system. The results show that the volcano is characterized by at least three main magma reservoirs at different depths: a basaltic reservoir at the Moho/lower crust depth, an intermediate reservoir at 10–15 km depth, and a shallower reservoir at 0.5–3 km depth. The shallower reservoir was involved in the ME eruption, which was triggered by a fresh trachytic melt entering a shallower reservoir where a comenditic magma was stored. The trachytes and comendites originate from fractional crystallization processes and minor assimilation of upper crust material, while the less evolved melts assimilate lower crust material. Syn-eruptive magma mingling occurred during the ME eruption phase. The magma reservoirs of the caldera-forming stage partly reactivate those of the cone-construction stage. The depth of the magma storage zones is controlled by the layering of the crust.The plumbing system of Changbaishan is vertically extensive, with crystal mush reservoirs renewed by the replenishment of new trachytic to trachyandesitic magma from depth. Unlike other volcanoes, evidence of a basaltic recharge is lacking. The interpretation of the signals preceding possible future eruptions should consider the multi-level nature of the Changbaishan plumbing system. A new arrival of magma may destabilize a part of or the entire system, thus triggering eruptions of different sizes and styles. The reference model proposed here for Changbaishan represents a prerequisite to properly understand periods of unrest to potentially anticipate future volcanic eruptions and to identify the mechanisms controlling the evolution of the crust below volcanoes.     

The 1783 Lakagigar eruption in Iceland: geochemistry,CO2 and sulfur degassing

About 12.3 km³ of basaltic magma were erupted from the Lakagigar fissure in Iceland in 1783, which may have been derived from the high-level reservoir of Grimsvotn central volcano, by lateral flow within the rifted crust. We have studied the petrology of quenched, glassy tephra from sections through pyroclastic cones along the fissure. The chemical composition of matrix glass of the 1783 tephra is heterogeneous and ranges from olivine tholeiite to Fe–Ti rich basalt, but the most common magma erupted is quartz tholeiite (Mg#43.6 to 37.2). The tephra are characterized by low crystal content (5 to 9 vol%). Glass inclusions trapped in plagioclase and Fo₈₆ to Fo₇₅ olivine phenocrysts show a large range of compositions, from primitive olivine tholeiite (Mg#64.3), quartz tholeiite (Mg#43–37), to Fe–Ti basalts (Mg#33.5) which represent the most differentiated liquids and are trapped as rare melt inclusions in clinopyroxene. Both matrix glass and melt inclusion data indicate a chemically heterogeneous magma reservoir, with quartz tholeiite dominant. LREE-depleted olivine-tholeiite melt-inclusions in Mg-rich olivine and anorthitic-plagioclase phenocrysts may represent primitive magma batches ascending into the reservoir at the time of the eruption. Vesicularity of matrix glasses correlates with differentiation, ranging from 10 to 60 vol.% in evolved quartz-tholeiite glasses, whereas olivine-tholeiite glasses contain less than 10 vol.% vesicles. FTIR analyses of olivine-tholeiite melt-inclusions indicate concentrations of 0.47 wt% H₂O and 430 to 510 ppm for CO₂. Chlorine in glass inclusions and matrix glasses increases from 50 ppm in primitive tholeiite to 230 ppm in Fe–Ti basalts, without clear evidence of degassing. Melt inclusion analyses show that sulfur varies from 915 ppm to 1970 ppm, as total FeO^* increases from 9 to 13.5 wt%. Sulfur degassing correlates both with vesicularity and magma composition. Thus sulfur in matrix glasses decreases from 1490 ppm to 500 ppm, as Mg # decreases from 47 to 37 and vesicularity of the magma strongly increases. These results indicate loss of at least 75% of sulfur during the eruption. The correlation of low sulfur content in matrix glasses with high vesicularity is regarded as evidence of the control of a major exsolving volatile phase on the degassing efficiency of the magma. Our model is consistent a quasi-permanent CO₂ flux through the shallow-level magmatic reservoir of Grimsvotn. Following magma withdrawal from the reservoir and during eruption from the Lakagigar fissure, sulfur degassing was controlled by inherent CO₂-induced vesicularity of the magma.     

Small volume andesite magmas and melt–mush interactions at Ruapehu, New Zealand: evidence from melt inclusions

Historical eruptions from Mt. Ruapehu (New Zealand) have been small (<0.001 km³ of juvenile magma) and have often occurred without significant warning. Developing better modelling tools requires an improved understanding of the magma storage and transport system beneath the volcano. Towards that end, we have analysed the volatile content and major element chemistry of groundmass glass and phenocryst-hosted melt inclusions in erupted samples from 1945 to 1996. We find that during this time period, magma has been stored at depths of ~2–9 km, consistent with inferences from geophysical data. Our data also show that Ruapehu magmas are relatively H₂O-poor (<2 wt%) and CO₂-rich (≤1,000 ppm) compared to typical arc andesites. Surprisingly, we find that melt inclusions are often more evolved than their transporting melt (as inferred from groundmass glass compositions). Furthermore, even eruptions that are separated by less than 2 years exhibit distinct major element chemistry, which suggests that each eruption involved magma with a unique ascent history. From these data, we infer that individual melt batches rise through, and interact with, crystal mush zones formed by antecedent magmas. From this perspective, we envision the magmatic system at Ruapehu as frequently recharged by small magma inputs that, in turn, cool and crystallise to varying degrees. Melts that are able to erupt through this network of crystal mush entrain (to a greater or lesser extent) exotic crystals. In the extreme case (such as the 1996 eruption), the resulting scoria contain melt inclusion-bearing crystals that are exotic to the transporting magma. Finally, we suggest that complex interactions between recharge and antecedent magmas are probably common, but that the small volumes and short time scales of recharge at Ruapehu provide a unique window into these processes.     

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.     

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.     

Merapi (Java,Indonesia): anatomy of a killer volcano

Merapi is Indonesia's most dangerous volcano with a history of deadly eruptions. Over the past two centuries, the volcanic activity has been dominated by prolonged periods of lava dome growth and intermittent gravitational or explosive dome failures to produce pyroclastic flows every few years. Explosive eruptions, such as in 2010, have occurred occasionally during this period, but were more common in pre‐historical time, during which a collapse of the western sector of the volcano occurred at least once. Variations in magma supply from depth, magma ascent rates and the degassing behaviour during ascent are thought to be important factors that control whether Merapi erupts effusively or explosively. A combination of sub‐surface processes operating at relatively shallow depth inside the volcano, including complex conduit processes and the release of carbon dioxide into the magmatic system through assimilation of carbonate crustal rocks, may result in unpredictable explosive behaviour during periods of dome growth. Pyroclastic flows generated by gravitational or explosive lava dome collapses and subsequent lahars remain the most likely immediate hazards near the volcano, although the possibility of more violent eruptions that affect areas farther away from the volcano cannot be fully discounted. In order to improve hazard assessment during future volcanic crises at Merapi, we consider it crucial to improve our understanding of the processes operating in the volcano's plumbing system and their surface manifestations, to generate accurate hazard zonation maps that make use of numerical mass flow models on a realistic digital terrain model, and to utilize probabilistic information on eruption recurrence and inundation areas.     

A mineral and cumulate perspective to magma differentiation at Nisyros volcano,Aegean arc

Lavas and pyroclastic products of Nisyros volcano (Aegean arc, Greece) host a wide variety of phenocryst and cumulate assemblages that offer a unique window into the earliest stages of magma differentiation. This study presents a detailed petrographic study of lavas, enclaves and cumulates spanning the entire volcanic history of Nisyros to elucidate at which levels in the crust magmas stall and differentiate. We present a new division for the volcanic products into two suites based on field occurrence and petrographic features: a low-porphyricity andesite and a high-porphyricity (rhyo)dacite (HPRD) suite. Cumulate fragments are exclusively found in the HPRD suite and are predominantly derived from upper crustal reservoirs where they crystallised under hydrous conditions from melts that underwent prior differentiation. Rarer cumulate fragments range from (amphibole-)wehrlites to plagioclase-hornblendites and these appear to be derived from the lower crust (0.5–0.8 GPa). The suppressed stability of plagioclase and early saturation of amphibole in these cumulates are indicative of high-pressure crystallisation from primitive hydrous melts (≥ 3 wt% H₂O). Clinopyroxene in these cumulates has Al₂O₃ contents up to 9 wt% due to the absence of crystallising plagioclase, and is subsequently consumed in a peritectic reaction to form primitive, Al-rich amphibole (Mg# > 73, 12–15 wt% Al₂O₃). The composition of these peritectic amphiboles is distinct from trace element-enriched interstitial amphibole in shallower cumulates. Phenocryst compositions and assemblages in both suites differ markedly from the cumulates. Phenocrysts, therefore, reflect shallow crystallisation and do not record magma differentiation in the deep arc crust.     

Millennial timescale resolution of rhyolite magma recharge at Tarawera volcano: insights from quartz chemistry and melt inclusions

Most rhyolite eruption episodes of Tarawera volcano have emitted several physiochemically distinct magma batches (∼1–10 km³). These episodes were separated on a millennial timescale. The magma batches were relatively homogeneous in temperature and composition at pumice scale (>4 cm), but experienced isolated crystallisation histories. At the sub-cm scale, matrix glasses have trace element compositions (Sr, Ba, Rb) that vary by factors up to 2.5, indicating incomplete mixing of separate melts. Some quartz-hosted melt inclusions are depleted in compatible trace elements (Sr, Ti, Ba) compared to enclosing matrix glasses. This could reflect re-melting of felsic crystals deeper in the crystal pile. Individual quartz crystals display a variety of cathodoluminescence brightness and Ti zoning patterns including rapid changes in melt chemistry and/or temperature (∼50–100°C), and point to multi-cycle crystallisation histories. The Tarawera magma system consisted of a crystal-rich mass containing waxing and waning melt pockets that were periodically recharged by silicic melts driven by basaltic intrusion. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

The magma plumbing system for the 1971 Teneguía eruption on La Palma,Canary Islands

The 1971 Teneguía eruption is the most recent volcanic event of the Cumbre Vieja rift zone on La Palma. The eruption produced basanite lavas that host xenoliths, which we investigate to provide insight into the processes of differentiation, assimilation and magma storage beneath La Palma. We compare our results to the older volcano magmatic systems of the island with the aim to reconstruct the temporal development of the magma plumbing system beneath La Palma. The 1971 lavas are clinopyroxene-olivine-phyric basanites that contain augite, sodic-augite and aluminium augite. Kaersutite cumulate xenoliths host olivine, clinopyroxene including sodic-diopside, and calcic-amphibole, whereas an analysed leucogabbro xenolith hosts plagioclase, sodic-augite-diopside, calcic-amphibole and hauyne. Mineral thermobarometry and mineral-melt thermobarometry indicate that clinopyroxene and plagioclase in the 1971 Teneguía lavas crystallised at 20–45 km depth, coinciding with clinopyroxene and calcic-amphibole crystallisation in the kaersutite cumulate xenoliths at 25–45 km and clinopyroxene, calcic-amphibole and plagioclase crystallisation in the leucogabbro xenolith at 30–50 km. Combined mineral chemistry and thermobarometry suggest that the magmas had already crystallised, differentiated and formed multiple crystal populations in the oceanic lithospheric mantle. Notably, the magmas that supplied the 1949 and 1971 events appear to have crystallised deeper than the earlier Cumbre Vieja magmas, which suggests progressive underplating beneath the Cumbre Vieja rift zone. In addition, the lavas and xenoliths of the 1971 event crystallised at a common depth, indicating a reused plumbing system and progressive recycling of Ocean Island plutonic complexes during subsequent magmatic activity.     

The Timescales of Magma Mixing in the Plumbing System of Bezymianny Volcano (Kamchatka): Insights from Diffusion Chronometry

Intrusion of magma of contrasting composition into a magma chamber often triggers eruptions of arc volcanoes. Application of the diffusion chronometry method allowed us to determine the time when fresh magma was supplied to the shallow chamber of Bezymianny volcano in the case of six eruptions in 2006–2012 and to compare them to the recorded seismic activity of this volcano. Two types of eruptions of Bezymianny volcano were distinguished, with a contrasting orthopyroxene rim being formed in the respective magmas (a) up to 3 years and (b) up to 2 months before the beginning of an eruption. It was shown that these differences are caused by two different paths of magma supply to the shallow chamber of Bezymianny volcano.     

Petrology of the 1979 eruption of Soufriere volcano,St. Vincent,Lesser Antilles

Major element, trace element, and Sr isotope data are used to study the temporal variation in the chemistry of the ejecta from the 1979 eruption of Soufriere volcano, St. Vincent, and to compare the compositions of the 1979 and 1971/2 magmas. Both the 1971/2 and 1979 products were basaltic andesites almost identical in petrography. A small temporal variation in chemistry is apparent in the 1979 samples but these cannot be related to the 1971/2 lava by fractional crystallisation of phenocryst phases, and the two eruptions may therefore have sampled different batches of magma. ⁸⁷Sr/⁸⁶Sr ratios of the two magmas were identical within analytical error.Microprobe analyses of phenocryst phases and glasses from the 1979 ejecta are presented. Clinopyroxene phenocryst cores with very high Mg/Fe ratios indicate that the basaltic andesites are products of fractionation of magnesian parents. Such magmas are represented by lavas on St. Vincent similar to the microphyric alkali picrites found to the south in Grenada. A common origin for the basaltic andesites of both islands by fractional crystallisation of picritic magmas is suggested. Dacitic glass is abundant in the groundmass of scoria blocks from the eruption. It does not represent the liquid originally in equilibrium with the phenocryst phases, but rather this liquid modified by quench crystallisation. Published interpretations suggesting that dacitic glass compositions in tephra from eruptions of the Soufriere are evidence of mixed-magma eruptions are therefore rejected.     

中国东部全新世火山的镭-钍同位素年代学

活火山是指1万年来有过喷发历史的全新世火山。火山的高分辨年代学对火山灾害评估和火山分类具有重要意义。对于缺乏历史记载的全新世火山,直接对火山岩进行同位素定年很困难。本文利用具有高时间分辨率的镭-钍-铀非平衡确定中国东部年轻火山的年龄。根据镭-钍-铀同位素,海南岛的马鞍岭和雷虎岭是全新世火山(马鞍岭:4.3ka;雷虎岭:4.7ka);镜泊湖火山(4.9ka)也是全新世火山;龙岗火山存在晚更新世和全新世活动(7.0ka,15.0ka);大兴安岭阿尔山和诺敏河Ra/Th非平衡消失但~(230)Th/~(238)U非平衡显著,属于晚更新世喷发(阿尔山:63ka;诺敏河:71ka)。海南岛的马鞍岭火山、雷虎岭火山和东北地区的龙岗火山、镜泊湖火山,是4座活火山。至于东北地区的阿尔山和诺敏河火山是否是活火山,有待测试更多样品的Ra/Th同位素。五大连池老黑山和火烧山有历史喷发记录,这与它们都存在显著Ra/Th非平衡一致。五大连池老黑山和火烧山的岩浆滞留年龄分别小于4.2ka和3.2ka,岩浆上升速率 18～23m/y。     

Mechanisms driving polymagmatic activity at a monogenetic volcano, Udo, Jeju Island, South Korea

High-resolution, stratigraphically ordered samples of the Udo tuff cone and lava shield offshore of Jeju Island, South Korea, show complex geochemical variation in the basaltic magmas that fed the eruption sequence. The eruption began explosively, producing phreatomagmatic deposits with relatively evolved alkali magma. The magma became more primitive over the course of the eruption, but the last magma to be explosively erupted had shifted back to a relatively evolved composition. A separate sub-alkali magma batch was subsequently effusively erupted to form a lava shield. Absence of weathering and only minor reworking between the tuff and overlying lava implies that there was no significant time break between the eruptions of the two magma batches. Modelling of the alkali magma suggests that it was generated from a parent melt in garnet peridotite at c. 3 to 3.5 GPa and underwent mainly clinopyroxene + olivine ± spinel fractionation at c. 1.5 to 2 GPa. The sub-alkali magma was, by contrast, generated from a chemically different peridotite with residual garnet at c. 2.5 GPa and evolved through olivine fractionation at a shallower level compared to its alkali contemporary. The continuous chemostratigraphic trend in the tuff cone, from relatively evolved to primitive and back to evolved, is interpreted to have resulted from a magma batch having risen through a single dyke and erupted the batch’s head, core and margins, respectively. The alkali magma acted as a path-opener for the sub-alkali magma. The occurrence of the two distinct batches suggests that different magmatic systems in the Jeju Island Volcanic Field have interacted throughout its history. The polymagmatic nature of this monogenetic eruption has important implications for hazard forecasting and for our understanding of basaltic field volcanism.     

From mush to eruption in centuries: assembly of the super-sized Oruanui magma body

The magmatic systems that give rise to voluminous crystal-poor rhyolite magma bodies can be considered to operate on two contrasting timescales: Those governed by longer-term processes by which a magma acquires its chemical and isotopic characteristics (e.g., fractional crystallisation and assimilation), and those operating at shorter timescales during the physical accumulation of the melt-dominant magma body that finally erupts. We explore the compositional and textural relationships between amphibole and orthopyroxene crystals from the 25.4 ka, 530 km³ (magma) Oruanui eruption products (Taupo volcano, New Zealand) to investigate how processes related to the physical assembly of the pre-eruptive magma body are represented in the crystal record. Over 90 % of orthopyroxenes from the volumetrically dominant high-SiO₂ (>74 wt%) rhyolite pumices record textural evidence for a significant disequilibrium event (partial dissolution ± resorption of cores and interiors) prior to the growth of 40–500 μm thick rim zones. This dissolution/regrowth history of orthopyroxene is recorded in the chemistry of co-crystallising amphiboles as a prominent inflection in the concentrations of Mn and Zn, two elements notably enriched in orthopyroxene relative to amphibole. Textural and chemical features, linked with in situ thermobarometric estimates, indicate that a major decompression event preceded the formation of the melt-dominant body. The decompression event is inferred to represent the extraction of large volumes of melt plus crystals from the Oruanui crystal mush/source zone at pressures of 140–300 MPa (~6–12 km depth). Orthopyroxene underwent partial dissolution during ascent before reestablishing in the melt-dominant magma body at pressures of 90–140 MPa (~3.5–6 km). We model Fe–Mg diffusion across the core-rim boundaries along the crystallographic a or b-axes to constrain the timing of this decompression event, which marked establishment of the melt-dominant magma body. Maximum modelled ages indicate that this event did not begin until ~1,600 years before eruption, consistent with constraints from zircon model-age spectra. Once extraction began, it underwent runaway acceleration with a peak extraction age of ~230 years, followed by an apparent period of stasis of ~60 years prior to eruption. The rapidity of the extraction and accumulation processes implies the involvement of a dynamic driving force which, in the rifted continental arc setting of the Taupo Volcanic Zone, seems likely to be represented by magma-assisted extensional tectonic processes.     

Primary melt from Sannome-gata volcano,NE Japan arc: constraints on generation conditions of rear-arc magmas

The conditions under which rear-arc magmas are generated were estimated using primary basalts from the Sannome-gata volcano, located in the rear of the NE Japan arc. Scoriae from the volcano occur with abundant crustal and mantle xenoliths, suggesting that the magma ascended rapidly from the upper mantle. The scoriae show significant variations in their whole-rock compositions (7.9–11.1 wt% MgO). High-MgO scoriae (MgO > ~9.5 wt%) have mostly homogeneous ⁸⁷Sr/⁸⁶Sr ratios (0.70318–0.70320), whereas low-MgO scoriae (MgO < ~9 wt%) have higher ⁸⁷Sr/⁸⁶Sr ratios (>0.70327); ratios tend to increase with decreasing MgO content. The high-MgO scoriae are aphyric, containing ~5 vol% olivine microphenocrysts with Mg# [100 × Mg/(Mg + Fe²⁺)] of up to 90. In contrast, the low-MgO scoriae have crustal xenocrysts of plagioclase, alkali feldspar, and quartz, and the mineralogic modes correlate negatively with whole-rock MgO content. On the basis of these observations, it is inferred that the high-MgO scoriae represent primary or near-primary melts, while the low-MgO scoriae underwent considerable interaction with the crust. Using thermodynamic analysis of the observed petrological features of the high-MgO scoriae, the eruption temperature of the magmas was constrained to 1,160–1,220 °C. Given that the source mantle was depleted MORB-source mantle, the primary magma was plausibly generated by ~7 % melting of a garnet-bearing spinel peridotite; taking this into consideration, and considering the constraints of multi-component thermodynamics, we estimated that the primary Sannome-gata magma was generated in the source mantle with 0.5–0.6 wt% H₂O at 1,220–1,230 °C and at ~1.8 GPa, and that the H₂O content of the primary magma was 6–7 wt%. The rear-arc Sannome-gata magma was generated by a lower degree of melting of the mantle at greater depths and lower temperatures than the frontal-arc magma from the Iwate volcano, which was also estimated to be generated by ~15 % melting of the source mantle with 0.6–0.7 wt% H₂O at ~1,250 °C and at ~1.3 GPa.     

Melt inclusion constraints on volatile systematics and degassing history of the 2014–2015 Holuhraun eruption,Iceland

The mass of volatiles emitted during volcanic eruptions is often estimated by comparing the volatile contents of undegassed melt inclusions, trapped in crystals at an early stage of magmatic evolution, with that of the degassed matrix glass. Here we present detailed characterisation of magmatic volatiles (H₂O, CO₂, S, Fl and Cl) of crystal-hosted melt and fluid inclusions from the 2014–2015 Holuhraun eruption of the Bárðarbunga volcanic system, Iceland. Based on the ratios of magmatic volatiles to similarly incompatible trace elements, the undegassed primary volatile contents of the Holuhraun parental melt are estimated at 1500–1700 ppm CO₂, 0.13–0.16 wt% H₂O, 60–80 ppm Cl, 130–240 ppm F and 500–800 ppm S. High-density fluid inclusions indicate onset of crystallisation at pressures?≥?0.4 GPa (~?12 km depth) promoting deep degassing of CO₂. Prior to the onset of degassing, the melt CO₂ content may have reached 3000–4000 ppm, with the total magmatic CO₂ budget estimated at  23–55 Mt. SO₂ release commenced at 0.12 GPa (~?3.6 km depth), eventually leading to entrapment of SO₂ vapour in low-density fluid inclusions. We calculate the syn-eruptive volatile release as 22.2 Mt of magmatic H₂O, 5.9–7.7 Mt CO₂, and 11.3 Mt of SO₂ over the course of the eruption; F and Cl release were insignificant. Melt inclusion constraints on syn-eruptive volatile release are similar to estimates made during in situ field monitoring, with the exception of H₂O, where field measurements may be heavily biased by the incorporation of meteoric water.