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     

Silicic magma entering a basaltic magma chamber: eruptive dynamics and magma mixing — an example from Salina (Aeolian islands,Southern Tyrrhenian Sea)

The Pollara tuff-ring resulted from two explosive eruptions whose deposits are separated by a paleosol 13 Ka old. The oldest deposits (LPP, about 0.2 km³) consist of three main fall units (A, B, C) deposited from a subplinian column whose height (7–14 km) increased with time from A to C, as a consequence of the increased magma discharge rate during the eruption (1–8x10⁶ kg/s). A highly variable juvenile population characterizes the eruption. Black, dense, highly porphyritic, mafic ejecta (SiO₂=50–55%) almost exclusively form A deposits, whereas grey, mildly vesiculated, mildly porphyritic pumice (SiO₂=56–67%) and white, highly vesiculated, nearly aphyric pumice (SiO₂=66–71%) predominate in B and C respectively. Mafic cumulates are abundant in A, while crystalline lithic ejecta first appear in B and increase upward. The LPP result from the emptying of an unusual and unstable, compositionally zoned, shallow magma chamber in which high density mafic melts capped low density salic ones. Evidence of the existence of a short crystal fractionation series is found in the mafic rocks; the andesitic pumice results from complete blending between rhyolitic and variously fractionated mafic melts (salic component up to 60 wt%), whereas bulk dacitic compositions mainly result from the presence of mafic xenocrysts within rhyolitic glasses. Viscosity and composition-mixing diagrams show that blended liquids formed when the visosities of the two end members had close values. The following model is suggested: 1. A rhyolitic magma rising through the metamorphic basement enterrd a mafic magma chamber whose souter portions were occupied by a highly viscous, mafic crystal mush. 2. Under the pressure of the rhyolitic body the nearly rigid mush was pushed upwards and mafic melts were squeezed against the walls of the chamber, beginning roof fracturing and mingling with silicic melts. 3. When the equilibrium temperature was reached between mafic and silicic melts, blended liquids rapidly formed. 4. When fractures reached the surface, the eruption began by the ejection of the mafic melts and crystal mush (A), followed by the emission of variously mingled and blended magmas (B) and ended by the ejection of nearly unmixed rhyolitic magma (C).     

Experimental constraints on pre-eruptive water contents and changing magma storage prior to explosive eruptions of Mount St Helens volcano

Compositionally diverse dacitic magmas have erupted from Mount St Helens over the last 4000 years. Phase assemblages and their compositions in these dacites provide information about the composition of the pre-eruptive melt, the phases in equilibrium with that melt and the magmatic temperature. From this information pre-eruptive pressures and water fugacities of many of the dacites have been inferred. This was done by conducting hydrothermal experiments at 850°C and a range of pressures and water fugacities and combining the results with those from experiments at temperatures of 780 and 920°C, to cover the likely range in equilibration conditions of the dacites. Natural phase assemblages and compositions were compared with the experimental results to infer the most likely conditions for the magmas prior to eruption. Water contents disolved in the melts of the dacites were then estimated from the inferred conditions. Water contents in the dacites have varied greatly, from 3.7 to 6.5 wt.%, in the last 4000 years. Between 4000 and about 3000 years ago the dacites tended to be water saturated and contained 5.5 to 6.5 wt.% water. Since then, however, the dacites have been significantly water-undersaturated and contained less than 5.0 wt.% water. These dacites have tended to be hotter and more mafic, and andesitic and basaltic magmas have erupted. These changes can be explained by variable amounts of mixing between felsic dacite and basalt, to produce hotter, drier and more mafic dacites and andesites. The magma storage region of the dacitic magmas has also varied significantly during the 4000 years, with shifts to shallower levels in the crust occurring within very short time periods, possibly even two years. These shifts may be related to fracturing of overlying roof rock as a result of magma with-drawal during larger volume eruptions.     

Petrology of lavas from episodes 2–47 of the Puu Oo eruption of Kilauea Volcano,Hawaii: Evaluation of magmatic processes

The Puu Oo eruption of Kilauea Volcano in Hawaii is one of its largest and most compositionally varied historical eruptions. The mineral and whole-rock compositions of the Puu Oo lavas indicate that there were three compositionally distinct magmas involved in the eruption. Two of these magmas were differentiated (<6.8 wt% MgO) and were apparently stored in the rift zone prior to the eruption. A third, more mafic magma (9–10 wt% MgO) was probably intruded as a dike from Kilauea's summit reservoir just before the start of the eruption. Its intrusion forced the other two magmas to mix, forming a hybrid that erupted during the first three eruptive episodes from a fissure system of vents. A new hybrid was erupted during episode 3 from the vent where Puu Oo later formed. The composition of the lava erupted from this vent became progressively more mafic over the next 21 months, although significant compositional variation occurred within some eruptive episodes. The intra-episode compositional variation was probably due to crystal fractionation in the shallow (0.0–2.9 km), dike-shaped (i.e. high surface area/volume ratio) and open-topped Puu Oo magma reservoir. The long-term compositional variation was controlled largely by mixing the early hybrid with the later, more mafic magma. The percentage of mafic magma in the erupted lava increased progressively to 100% by episode 30 (about two years after the eruption started). Three separate magma reservoirs were involved in the Puu Oo eruption. The two deeper reservoirs (3–4 km) recharged the shallow (0.4–2.9 km) Puu Oo reservoir. Recharge of the shallow reservoir occurred rapidly during an eruption indicating that these reservoirs were well connected. The connection with the early hybrid magma body was cut off before episode 30. Subsequently, only mafic magma from the summit reservoir has recharged the Puu Oo reservoir.     

Precursory activity of the 161 ka Kos Plateau Tuff eruption, Aegean Sea (Greece)

The Kos Plateau Tuff (KPT) eruption of 161 ka was the largest explosive Quaternary eruption in the eastern Mediterranean. We have discovered an uplifted beach deposit of abraded pumice cobbles, directly overlain by the KPT. The pumice cobbles resemble pumice from the KPT in petrography and composition and differ from Plio-Pleistocene rhyolites on the nearby Kefalos Peninsula. The pumice contains enclaves of basaltic andesite showing chilled lobate margins, suggesting co-existence of two magmas. The deposit provides evidence that the precursory phase of the KPT eruption produced pumice rafts, and defines the paleoshoreline for the KPT, which elsewhere was deposited on land. The beach deposit has been uplifted about 120 m since the KPT eruption, whereas the present marine area south of Kos has subsided several hundred metres, as a result of regional neotectonics. The basaltic andesite is more primitive than other mafic rocks known from the Kos–Nisyros volcanic centre and contains phenocrysts of Fo₈₉ olivine, bytownite, enstatite and diopside. Groundmass amphibole suggests availability of water in the final stages of magma evolution. Geochemical and mineralogical variation in the mafic products of the KPT eruption indicate that fractionation of basaltic magma in a base-of-crust magma chamber was followed by mixing with rhyolitic magma during eruption. Low eruption rates during the precursory activity may have minimised the extent of mixing and preserved the end-member magma types.     

Petrology of lavas from the Puu Oo eruption of Kilauea Volcano: III. The Kupaianaha episode (1986–1992)

 The Puu Oo eruption has been remarkable in the historical record of Kilauea Volcano for its duration (over 13 years), volume (>1 km³) and compositional variation (5.7–10 wt.% MgO). During the summer of 1986, the main vent for lava production moved 3 km down the east rift zone and the eruption style changed from episodic geyser-like fountaining at Puu Oo to virtually continuous, relatively quiescent effusion at the Kupaianaha vent. This paper examines this next chapter in the Puu Oo eruption, episodes 48 and 49, and presents new ICP-MS trace element and Pb-, Sr-, and Nd-isotope data for the entire eruption (1983–1994). Nearly aphyric to weakly olivine-phyric lavas were erupted during episodes 48 and 49. The variation in MgO content of Kupaianaha lavas erupted before 1990 correlates with changes in tilt at the summit of Kilauea, both of which probably were controlled by variations in Kilauea's magma supply rate. These lavas contain euhedral olivines which generally are in equilibrium with whole-rock compositions, although some of the more mafic lavas which erupted during 1990, a period of frequent pauses in the eruption, accumulated 2–4 vol.% olivine. The highest forsterite content of olivines (∼85%) in Kupaianaha lavas indicates that the parental magmas for these lavas had MgO contents of ∼10 wt.%, which equals the highest observed value for lavas during this eruption. The composition of the Puu Oo lavas has progressively changed during the eruption. Since early 1985 (episode 30), when mixing between an evolved rift zone magma and a more mafic summit reservoir-derived magma ended, the normalized (to 10 wt.% MgO) abundances of highly incompatible elements and CaO have systematically decreased with time, whereas ratios of these trace elements and Pb, Sr, and Nd isotopes, and the abundances of Y and Yb, have remained relatively unchanged. These results indicate that the Hawaiian plume source for Puu Oo magmas must be relatively homogeneous on a scale of 10–20 km³ (assuming 5–10% partial melting), and that localized melting within the plume has apparently progressively depleted its incompatible elements and clinopyroxene component as the eruption continued. The rate of variation of highly incompatible elements in Puu Oo lavas is much greater than that observed for Kilauea historical summit lavas (e.g., Ba/Y 0.09 a^–1 vs ∼0.03 a^–1). This rapid change indicates that Puu Oo magmas did not mix thoroughly with magma in the summit reservoir. Thus, except for variable amounts of olivine fractionation, the geochemical variation in these lavas is predominantly controlled by mantle processes. Received: 8 March 1996 / Accepted: 30 April 1996     

Magma mixing recorded in intermediate rocks associated with high-Mg andesites from the Setouchi volcanic belt, Japan: implications for Archean TTG formation

Calc-alkaline intermediate rocks are spatially and temporally associated with high-Mg andesites (HMAs, Mg#>60) in Middle Miocene Setouchi volcanic belt. The calc-alkaline rocks are characterized by higher Mg# (strongly calc-alkaline trend) than ordinary calc-alkaline rocks at equivalent silica contents. Phenocrysts in the intermediate rocks have petrographical features such as: (1) coexisting reversely and normally zoned orthopyroxene phenocrysts in single rock; (2) sieve type plagioclase in which cores are mantled by higher An%, melt inclusion-rich zone; and (3) reversely zoned amphibole phenocrysts with opacite cores. In addition, mingling textures and magmatic inclusions were observed in some rocks. These petrographic features and the mineral chemistry indicate that magma mixing was the most important process in producing the strongly calc-alkaline rocks. The core composition of normally zoned orthopyroxene phenocrysts and the mantle composition of reversely zoned orthopyroxene phenocrysts have relatively high Mg# (85–90) in maximum. Although basaltic and high-Mg andesitic magmas are candidate as possible mafic end-member magmas, basaltic magma is excluded in terms of phenocryst assemblage and bulk composition. HMA magmas are suitable mafic end-member magmas that precipitated high Mg# (90) orthopyroxene, whereas andesitic to dacitic magma are suitable felsic end-members. In contrast, it is difficult to produce the strongly calc-alkaline trend through fractional crystallization from a HMA magma, because it would require removal of plagioclase together with mafic minerals from the early stage of crystallization, whereas the precipitation of plagiolase is suppressed due to the high water content of HMA magmas. These results imply that Archean Mg#-rich TTGs (>45–55), which are an analog of the strongly calc-alkaline rocks in terms of chemistry and magma genesis, can be derived from magma mixing in which a HMA magma is the mafic end-member magma, rather than by fractional crystallization from a HMA magma.     

Petrologic investigations of the 1995 and 1996 eruptions of Ruapehu volcano, New Zealand: formation of discrete and small magma pockets and their intermittent discharge

 Ruapehu volcano erupted intermittently between September and November 1995, and June and July 1996, producing juvenile andesitic scoria and bombs. The volcanic activity was characterized by small, sequential phreatomagmatic and strombolian eruptions. The petrography and geochemistry of dated samples from 1995 (initial magmatic eruption of 18 September 1995, and two larger events on 23 September and 11 October), and from 1996 (initial and larger eruptions on 17–18 June) suggest that episodes of magma mixing occurred in separate magma pockets within the upper part of the magma plumbing system, producing juvenile andesitic magma by mixing between relatively high (1000–1200  °C)- and low (∼1000  °C)- temperature (T) end members. Oscillatory zoning in pyroxene phenocrysts suggests that repeated mixing events occurred prior to and during the 1995 and 1996 eruptions. Although the 1995 and 1996 andesitic magmas are products of similar mixing processes, they display chronological variations in phenocryst clinopyroxene, matrix glass, and whole-rock compositions. A comparison of the chemistry of magnesian clinopyroxene in the four tephras indicates that, from 18 September through June 1996, the tephras were derived from at least two discrete high-temperature (high-T) batches of magma. Crystals of magnesian clinopyroxene in the 23 September and 11 October tephras appear to be derived from different high-T magma batches. Whole-rock and matrix-glass compositions of all tephras are consistent with their derivation from distinct mixed melts. We propose that, prior to 1995 there was a shallow low-temperature (low-T) magma storage system comprising crystal-rich mush and remnant magma from preceding eruptive episodes. Crystal clots and gabbroic inclusions in the tephras attest to the existence of relict crystal mush. At least two discrete high-T magmas were then repeatedly injected into the mush zone, forming discrete and mixed magma pockets within the shallow system. The intermittent 1995 and 1996 eruptions sequentially tapped these magma pockets. Received: 1 April 1998 / Accepted: 22 December 1998     

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.     

Influence of pre-eruptive storage conditions and volatile contents on explosive Plinian style eruptions of basic magma

Sub-Plinian to Plinian eruptions of basic magma present a challenge to modeling volcanic behavior because many models rely on magma becoming viscous enough during ascent to behave brittlely and cause fragmentation. Such models are unable, however, to strain low viscosity magma fast enough for it to behave brittlely. That assumes that such magmas actually have low viscosities, but the rare Plinian eruptions of basic magma may in fact result from them being anomalously viscous. Here, we examine two such eruptions, the 122 B.C. eruption of hawaiitic basalt from Mt. Etna and the late Pleistocene eruption of basaltic andesite from Masaya Caldera, to test whether they were anomalously viscous. We carried out hydrothermal experiments on both magmas and analyzed glass inclusions in plagioclase phenocrysts from each to determine their most likely pre-eruptive temperatures and water contents. We find that the hawaiite was last stored at 1,000–1,020°C, whereas the basaltic andesite was last stored at 1,010–1,060°C, and that both were water saturated with ∼3.0 wt.% water dissolved in them. Such water contents are not high enough to trigger Plinian explosive behavior, as much more hydrous basic magmas erupt less violently. In addition, despite being relatively cool, the viscosities of both magmas would range from ∼10^2.2–2.5 Pa s before erupting to ∼10⁴ Pa s when essentially degassed, all of which are too fluid to cause brittle disruption. Without invoking special external forces to explain all such eruptions, one of the more plausible explanations is that when the bubble content reaches some critical value the fragile foam-like magma disrupts. The rarity of Plinian eruptions of basic magma may be because such magmas must ascend fast enough to retain their bubbles.     

Petrology and sulfur and chlorine emissions of the 1963 eruption of Gunung Agung,Bali, Indonesia

 The 1963 eruption of Gunung Agung produced 0.95 km³ dense rock equivalent (DRE) of olivine±hornblende-bearing, weakly phyric, basaltic andesite tephra and lava. Evidence for magma mixing in the eruptive products includes whole-rock compatible and incompatible trace element trends, reverse and complex compositional zoning of mineral phases, disequilibrium mineral assemblages, sieve-textured plagioclase phenocrysts, and augite rims on reversely zoned orthopyroxene. Basalt magma mixed with pre-existing andesite magma shortly before eruption to yield basaltic andesite with a temperature of 1040–1100  °C at an assumed pressure of 2 kb, f O₂>NNO, and an average melt volatile content (H₂O±CO₂) of 4.3 wt.%. Magma-mixing end members may have provided some of the S and Cl emitted in the eruption. Glass inclusions in phenocrysts contain an average of 650 ppm S and 3130 ppm Cl as compared with 70 ppm and 2220 ppm, respectively, in the matrix glass. Maximum S and Cl contents of glass inclusions approach 1800 and 5000 ppm, respectively. Application of the petrologic method to products of the 1963 eruption for estimating volatile release yields of 2.5×10¹²g (Mt) of SO₂ and 3.4 Mt of Cl released from the 0.65 km³ of juvenile tephra which contributed to stratospheric injection of H₂SO₄ aerosols on 17 March and 16 May, when eruption column heights exceeded 20 km above sea level. An independent estimate of SO₂ release from atmospheric aerosol loading (11–12 Mt) suggests that approximately 7 Mt of SO₂ was injected into the stratosphere. The difference between the two estimates can be most readily accounted for by the partitioning of S, as well as some Cl, from the magma into a water-rich vapor phase which was released upon eruption. For other recent high-S-release eruptions of more evolved and oxidized magmas (El Chichón, Pinatubo), the petrologic method gives values two orders of magnitude less than independent estimates of SO₂ emissions. Results from this study of the Agung 1963 magma and its volatile emissions, and from related studies on eruptions of more mafic magmas, suggest that SO₂ emissions from eruptions of higher-S-solubility magma may be more reliably estimated by the petrologic method than may those from more-evolved magma eruptions. Received: 29 June 1994 / Accepted: 25 April 1996     

Temporal variations in magma composition at Merapi Volcano (Central Java, Indonesia): magmatic cycles during the past 2000 years of explosive activity

Merapi Volcano (Central Java, Indonesia) has been frequently active during Middle to Late Holocene time producing basalts and basaltic andesites of medium-K composition in earlier stages of activity and high-K magmas from 1900 ¹⁴C yr BP to the present. Radiocarbon dating of pyroclastic deposits indicates an almost continuous activity with periods of high eruption rates alternating with shorter time spans of distinctly reduced eruptive frequency since the first appearance of high-K volcanic rocks. Geochemical data of 28 well-dated, prehistoric pyroclastic flows of the Merapi high-K series indicate systematic cyclic variations. These medium-term compositional variations result from a complex interplay of several magmatic processes, which ultimately control the periodicity and frequency of eruptions at Merapi. Low eruption rates and the absence of new influxes of primitive magma from depth allow the generation of basaltic andesite magma (56–57 wt% SiO₂) in a small-volume magma reservoir through fractional crystallisation from parental mafic magma (52–53 wt% SiO₂) in periods of low eruptive frequency. Magmas of intermediate composition erupted during these stages provide evidence for periodic withdrawal of magma from a steadily fractionating magma chamber. Subsequent periods are characterised by high eruption rates that coincide with shifts of whole-rock compositions from basaltic andesite to basalt. This compositional variation is interpreted to originate from influxes of primitive magma into a continuously active magma chamber, triggering the eruption of evolved magma after periods of low eruptive frequency. Batches of primitive magma eventually mix with residual magma in the magmatic reservoir to decrease whole-rock SiO₂ contents. Supply of primitive magma at Merapi appears to be sufficiently frequent that andesites or more differentiated rock types were not generated during the past 2000 years of activity. Cyclic variations also occurred during the recent eruptive period since AD 1883. The most recent eruptive episode of Merapi is characterised by essentially uniform magma compositions that may imply the existence of a continuously active magma reservoir, maintained in a quasi-steady state by magma recharge. The whole-rock compositions at the upper limit of the total SiO₂ range of the Merapi suite could also indicate the beginning of another period of high eruption rates and shifts towards more mafic compositions.     

Heterogeneous andesite–dacite ejecta in 26–16.6 ka pyroclastic deposits of Tongariro Volcano,New Zealand: the product of multiple magma-mixing events

The previously poorly documented 26–16.6 ka interval of pyroclastic volcanism from Tongariro Volcano is marked by three distal lapilli fall units (Rt1-3) exposed in ring-plain deposits. The distal Rt1-3 units are tentatively correlated to proximal scoria deposits on the upper slopes of North Crater based on their dispersal patterns, petrography and geochemistry. Lapilli in each of the Rt1-3 deposits are characterised by variable groundmass crystallinity, vesicularity and colour within individual clasts. Matrix glasses are mostly microlite-free, and compositionally diverse across the deposits (SiO₂ = 62–75 wt%), with wide composition ranges occurring within single clasts. The glasses represent different melts that were mingled and mixed shortly before eruption; a finding supported by widely variable Fe–Ti oxide equilibrium temperature estimates (∼830–1,200°C). Ranges of 30–160°C (typically 70°C) occur within individual clasts. Some clinopyroxene crystals display Mg-rich (∼Mg #88) rim zones around homogeneous low-Mg (∼Mg #68) cores, with abrupt transition zones. This zoning is interpreted as resulting from the injection of a more mafic melt into a stagnating, resident magma. Crystal-melt equilibria indicate that several episodes of mafic intrusion occurred, to produce hybrid melts with zoned crystals forming isolated ponds within the resident magma. Variable mixing from the percolation of melts and the coalescence of melt ponds would explain the wide range of melt compositions and equilibrium temperatures observed in the ejecta. The magma heterogeneity was preserved by quenching on prompt eruption, with much of the short-duration chaotic mixing of melts and crystals occurring in the conduit. The Rt1-3 eruptions were from an open magmatic system consisting of one or more long-lived stagnant crystal mush zones, from which eruptions were rapidly triggered by new injections of mafic magmas from greater depths. A similar pattern of magmatic dynamics was observed in the much smaller 1995 eruptions of the neighbouring Ruapehu Volcano.     

Large glass inclusions in plagioclase phenocrysts and their bearing on the origin of mixed andesitic lavas at Tolimán volcano,Guatemala

Irregularly shaped, large and clear (LAC) glass inclusions are present in plagioclase phenocrysts in several andesitic lavas erupted from Tolimán volcano, Guatemala. Their morphology is different from densely spaced, fine-grained glass inclusions that form concentric zones in dusty or cellular textured plagioclase phenocrysts. The large size of LAC inclusions make them suitable for microprobe analysis and average bulk compositions are presented for glasses in 30 phenocrysts from eight lava samples. Their compositions are rhyolitic and in disequilibrium, or out-range (Anderson 1976) with respect to whole-rock and groundmass glass compositions. LAC inclusions typically occur in large, tabular plagioclase phenocrysts with relatively uniform, sodic compositions (An 40–54). Compositions of feldspar phenocrysts not containing LAC inclusions range from An 41 to An 81. Petrographic and chemical data support a primary origin for LAC glasses, suggest mixing of mafic and silicic magmas, and also constrain a mechanism for magma mixing. Rapid growth of plagioclase and entrapment of LAC glass occurs during mixing in a vapor-rich silicic liquid under low degrees of undercooling. These conditions are possibly produced in a high-level magma body such as that envisioned by Huppert et al. (1982), where replenishment and subsequent crystallization of a hydrous magma induces density instability and mixing with the resident magma.     

Major changes in the post-glacial evolution of magmatic compositions and pre-eruptive conditions of Llaima Volcano,Andean Southern Volcanic Zone,Chile

Llaima is one of the most active volcanoes of the Chilean volcanic front with recent explosive eruptions in 2008 and 2009. Understanding how the volcano evolved to its present state is essential for predictions of its future behavior. The post-glacial succession of explosive volcanic eruptions of Llaima stratovolcano started with two caldera-forming eruptions at ～16 and ～15 ka, that emplaced two large-volume basaltic-andesitic ignimbrites (unit I). These are overlain by a series of fall deposits (unit II) changing from basaltic-andesitic to dacitic compositions with time. The prominent compositionally zoned, dacitic to andesitic Llaima pumice (unit III) was formed by a large Plinian eruption at ～10 ka that produced andesitic surge deposits (unit IV) in its terminal phase. The following unit V represents a time interval of ～8,000 years during which at least 30 basaltic to andesitic ash and lapilli fall deposits with intercalated volcaniclastic sediments and paleosols were emplaced. Bulk rock, mineral, and glass chemical data constrain stratigraphic changes in magma compositions and pre-eruptive conditions that we interpret in terms of four distinct evolutionary phases. Phase 1 (=unit I) magmas have lower large ion lithophile (LIL)/high field strength (HFS) element ratios compared to younger magmas and thus originated from a mantle source less affected by slab-derived fluids. They differentiated in a reservoir at mid-crustal level. During the post-caldera phase 2 (=units II–IV), relatively long residence times between eruptions allowed for increasingly differentiated magmas to form in a reservoir in the middle crust. Fractional crystallization led to volatile enrichment and oversaturation and is the driving force for the large Plinian eruption of the most evolved (unit III) dacite at Llaima, although replenishment by hot andesite probably triggered the eruption. During the subsequent phase 3 (=unit V >3 ka), frequent mafic replenishments at mid-crustal storage levels favored shorter residence times limiting erupted magma compositions to water-undersaturated basaltic andesites and andesites. At around 3 ka, the magma storage level for phase 4 (=unit V <3 ka to present) shifted to the uppermost crust where the hot magmas partly assimilated the granitic country rock. Although water contents of these basaltic andesites were low, the low-pressure storage facilitated water saturation before eruption. The change in magma storage level at 3 ka was responsible for the dramatic increase in eruption frequency compared to the older Llaima history. We suggest that the change from middle to upper crust magma storage is caused by a change in the stress regime below Llaima from transpression to tension.     

The Negra Muerta Volcanic Complex, southern Central Andes: geochemical characteristics and magmatic evolution of an episodically active volcanic centre

This petrologic analysis of the Negra Muerta Volcanic Complex (NMVC) contributes to understanding the magmatic evolution of eruptive centres associated with prominent NW-striking fault zones in the southern Central Andes. Specifically, the geochemical characteristics and magmatic evolution of the two eruptive episodes of this Complex are analysed. The first one occurred as an explosive eruption at 9 Ma and is represented by a strongly welded, fiamme-rich, andesitic to dacitic ignimbrite deposit. The second commenced with an eruption of a rhyolitic ignimbrite at 7.6 Ma followed by effusive discharge of hybrid lavas at 7.3 Ma and by emplacement of andesitic to rhyodacitic dykes and domes. Both explosive and effusive eruptions of the second episode occurred within a short time span, but geochemical interpretations permit consideration of the existence of different magmas interacting in the same magma chamber. Our model involves an andesitic recharge into a partially cooled rhyolitic magma chamber, pressurising the magmatic system and triggering explosive eruption of rhyolitic magma. Chemical or mechanical evidence for interaction between the rhyolitic and andesitic magma in the initial stages are not obvious because of their difference in composition, which could have been strong enough to inhibit the interaction between the two magmas. After the initial explosive stages of the eruption at 7.6 Ma, the magma chamber become more depressurised and the most mafic magma settled in compositional layers by fractional crystallisation. Restricted hybridisation occurred and was effective between adjacent and thermally equivalent layers close to the top of the magma chamber. At 7.3 Ma, increments of caldera formation were accompanied by effusive discharge of hybrid lavas through radially disposed dykes whereby andesitic magma gained in importance toward the end of this effusive episode in the central portion of the caldera. Assimilation during turbulent ascent (ATA) is invoked to explain a conspicuous reversed isotopic signature (⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd) in the entire volcanic series. Therefore, the 7.6 to 7.3 Ma volcanic rocks of the NMVC resulted from synchronous and mutually interacting petrological processes such as recharge, fractional crystallization, hybridisation, and Assimilation during Turbulent Ascent (ATA).Geochemical characteristics of both volcanic episodes show diverse type and/or depth in the sources and variable influence of upper crustal processes, and indicate a recurrence in the magma-forming conditions. Similarly, other minor volcanic centres in the transversal volcanic belts of the Central Andes repeated their geochemical signatures throughout the Miocene.     

Geochemical homogeneity of a long-lived,large silicic system; evidence from the Cerro Galán caldera,NW Argentina

By applying a number of analytical techniques across a spectrum of spatial scales (centimeter to micrometer) in juvenile components, we show that the Cerro Galán volcanic system has repeatedly erupted magmas with nearly identical geochemistries over >3.5 Myr. The Cerro Galán system produced nine ignimbrites (∼5.6 to 2 Ma) with a cumulative volume of >1,200 km³ (DRE; dense rock equivalent) of calc-alkaline, high-K rhyodacitic magmas (68–71 wt.% SiO₂). The mineralogy is broadly constant throughout the eruptive sequence, comprising plagioclase, quartz, biotite, Fe–Ti oxides, apatite, and titanite. Early ignimbrite magmas also contained amphibole, while the final eruption, the most voluminous Cerro Galán ignimbrite (CGI; 2.08 ± 0.02 Ma) erupted a magma containing rare amphibole, but significant sanidine. Each ignimbrite contains two main juvenile clast types; dominant “white” pumice and ubiquitous but subordinate “grey” pumice. Fe–Ti oxide and amphibole-plagioclase thermometry coupled with amphibole barometry suggest that the grey pumice originated from potentially hotter and deeper magmas (800–840°C, 3–5 kbar) than the more voluminous white pumice (770–810°C, 1.5–2.5 kbar). The grey pumice is interpreted to represent the parental magmas to the Galán system emplaced into the upper crust from a deeper storage zone. Most inter-ignimbrite variations can be accounted for by differences in modal mineralogy and crystal contents that vary from 40 to 55 vol.% on a vesicle-free basis. Geochemical modeling shows that subtle bulk-rock variations in Ta, Y, Nb, Dy, and Yb between the Galán ignimbrites can be reconciled with differences in amounts of crystal fractionation from the “grey” parent magma. The amount of fractionation is inversely correlated with volume; the CGI (∼630 km³) and Real Grande Ignimbrite (∼390 km³) return higher F values (proportion of liquid remaining) than the older Toconquis Group ignimbrites (<50 km³), implying less crystal fractionation took place during the upper-crustal evolution of these larger volume magmas. We attribute this relationship to variations in magma chamber geometry; the younger, largest volume ignimbrites came from flat sill-like magma chambers, reducing the relative proportion of sidewall crystallization and fractionation compared to the older, smaller-volume ignimbrite eruptions. The grey pumice clasts also show evidence of silicic recharge throughout the history of the Cerro Galán system, and recharge days prior to eruption has previously been suggested based on reversely zoned (OH and Cl) apatite phenocrysts. A rare population of plagioclase phenocrysts with thin An-rich rims in juvenile clasts in many ignimbrites supports the importance of recharge in the evolution and potential triggering of eruptions. This study extends the notion that large volumes of nearly identical silicic magmas can be generated repeatedly, producing prolonged geochemical homogeneity from a long-lived magma source in a subduction zone volcanic setting. At Cerro Galán, we propose that there is a zone between mantle magma input and upper crustal chambers, where magmas are geochemically “buffered”, producing the underlying geochemical and isotopic signatures. This produces the same parental magmas that are delivered repeatedly to the upper crust. A lower-crustal MASH (melting, assimilation, storage, and homogenization) zone is proposed to act as this buffer zone. Subsequent upper crustal magmatic processes serve only to slightly modify the geochemistry of the magmas.     

The Pleistocene cinder cones surrounding Volcán Colima, Mexico re-visited: eruption ages and volumes, oxidation states, and sulfur content

Located at the volcanic front in the western Mexican arc, in the Colima Rift, is the active Volcán Colima, which lies on the southern end of the massive (∼450 km³) Colima-Nevado volcanic complex. Along the margins of this andesitic volcanic complex, is a group of 11 scoria cones and associated lavas, which have been dated by the ⁴⁰Ar/³⁹Ar method. Nine scoria cones erupted ∼1.3 km³ of alkaline magma (basanite, leucite-basanite, minette) between 450 and 60 ka, with >99% between 240 and 60 ka. Two additional cones (both the oldest and calc-alkaline) erupted <0.003 km³ of basalt (0.5 Ma) and <0.003 km³ of basaltic andesite (1.2 Ma), respectively. Cone and lava volumes were estimated with the aid of digital elevation models (DEMs). The eruption rate for these scoria cones and their associated lavas over the last 1.2 Myr is ∼1.2 km³/Myr, which is more than 400 times smaller than that from the andesitic Colima-Nevado edifice. In addition to these alkaline Colima cones, two other potassic basalts erupted at the volcanic front, but ∼200 km to the ESE (near the historically active Volcán Jorullo), and were dated at 1.06 and 0.10 Ma. These potassic suites reflect the tendency in the west-central Mexican arc for magmas close to the volcanic front to be enriched in K₂O relative to those farther from the trench.Ferric-ferrous analyses on pristine samples from the alkaline cones adjacent to V. Colima and V. Jorullo indicate that their oxygen fugacities relative to the nickel-nickel oxide buffer are significantly higher (ΔNN0=2–4) than those for the calc-alkaline magma types (0–1.5). These ΔNNO values correlate positively with Ba concentrations and likely reflect the influence of a slab-derived fluid. As a result of the high oxidation states, the solubility of sulfur in these potassic magmas is enhanced. Indeed the sulfur content of both the whole rock and the apatite phenocrysts (and in olivine melt inclusions reported in the literature) suggest that part of their pre-eruptive sulfur gas (SO₂) concentrations could have been discharged to the atmosphere in amounts comparable to the 1982 eruption of El Chichón, although over a prolonged period spanning thousands of years (not per eruption).Electronic Supplementary Material Supplementary material is available for this article at Editorial responsibility: J. Donnelly-Nolan     

Petrology and Fe–Ti oxide reequilibration of the 1991 Mount Unzen mixed magma

A dacitic magma (64.5 wt.% SiO₂), a mixture of phenocryst-rich rhyodacite and an aphyric mafic magma, was erupted during the recent 1991–1995 Mount Unzen eruptive cycle. The experimental and analytical results of this study reveal additional details about conditions in the premixing and postmixing magmas, and the nature of the mixing process. The preeruption rhyodacitic magma was at a temperature of 790±20°C according to Fe–Ti oxide phenocryst cores, and at a depth of 6 to 7 km (160 MPa) according to Al-in-hornblende geobarometry. The mafic magma that mixed with the rhyodacite is found as andesitic (54 to 62 wt.% SiO₂) enclaves in the erupted magma and was essentially aphyric when intruded. Phase equilibria indicate that an aphyric andesite at 160 MPa is >1030°C (H₂O-saturated) and possibly as high as 1130°C (2 wt.% H₂O). The composition of the rhyodacite which was mixed with the andesite is estimated to lie between 67 and 69 wt.% SiO₂. Using these compositions and temperatures, the temperature of the Unzen magma after mixing is estimated to be at least 850° to 870°C. The groundmass Fe–Ti oxide microphenocrysts and those in pargasite-bearing reaction zones around biotite phenocrysts both give 890±20°C temperatures; the oxide–oxide contacts give temperatures of 910±20°C. The 900±30°C postmixing temperatures are consistent with phase-equilibria experiments which show that the magma was not above 930°C at 160 MPa. Our Fe–Ti oxide reequilibration experiments suggest that the mixing of the two magmas began within a few weeks of the eruption, which is a shorter time than is calculated using available diffusion data. There is also evidence that some mixing took place much closer to the time of extrusion based on the presence of unrimmed biotite phenocrysts in the magma.     

Eruptive history and magmatic evolution of the 1.9 kyr Plinian dacitic Chiltepe Tephra from Apoyeque volcano in west-central Nicaragua

The youngest dacitic Plinian eruption in west-central Nicaragua, forming the 18 km³ Chiltepe Tephra (CT), occurred about nineteen hundred years ago at Apoyeque stratovolcano, which dominates the Chiltepe volcanic complex 15 km north of the capital Managua, where the CT is 2 m thick. We have traced the CT from its proximal facies at the crater rim, through the medial facies in the lowlands around Apoyeque, and to the distal facies up to 550 km offshore in the Pacific. While medial and distal facies consist of widespread Plinian fall deposits, the proximal facies reveals the complexity of this eruption, which we divide into four phases (I–IV). Interaction of rising magma with a pre-existing crater lake generated the phreatomagmatic opening phase I of the eruption, which produced ash fall with accretionary lapilli. Phase II marked a rapid change to persistent magmatic activity that yielded several large Plinian eruptions, declining through a period of unstable eruption conditions, followed by a short hiatus. Phase III began with unstable conditions, probably as a result of eastward migration and widening of the vent, leading to a second period of Plinian eruptions with three major events reaching magma discharge rates five times larger than those of phase II. Phase III again declined through unstable eruption conditions before magmatic activity terminated. Numerous explosions in the shallow hydrothermal system during the final phase IV resulted in the formation of a phreatic tuff ring on the rim of Apoyeque crater. The white, highly-vesicular, dacitic CT pumice contains plagioclase (An_45–68), orthopyroxene, clinopyroxene, and minor hornblende, apatite and titanomagnetite phenocrysts. A very subordinate fraction of gray pumice has the highest crystal content, the least evolved bulk-rock, but the most evolved matrix-glass composition. The CT dacite has two unusual compositional features: (1) all white dacite has the same melt (matrix-glass) composition such that variations in bulk-rock compositions (64–68 wt% SiO₂) simply reflect different phenocryst contents of 10–35%, interpreted as the result of gradual phenocryst settling in the magma chamber. (2) Abundant olivine crystals with a bimodal distribution in Mg# (modes at Mg# = 0.75 and Mg# = 0.8) are dispersed throughout the erupted dacite. These are clearly out of equilibrium with the dacitic melt and are interpreted as xenocrysts derived from the basaltic Nejapa-Miraflores volcanic lineament that intersects the Chiltepe volcanic complex and was contemporaneously active. Thermobarometric estimates place the dacitic CT magma reservoir in the upper crust (<250 MPa), with a temperature of about 890°C and about 5 wt% water dissolved in the melt. Comparing water and chlorine contents with respective solubility models suggests that volatile degassing began in the magma reservoir and triggered the CT eruption. From the vertical compositional variation pattern of the CT we deduce that the conduit tapped the magma chamber not at the top but from the side, at some deeper level, and that subsequent magma withdrawal was governed by both variations in discharge rate and possible upward migration and/or widening of the conduit entrance.