Intracrustal origin of Arenal basaltic andesite in the light of solid–melt interactions and related compositional buffering

The origin of Arenal basaltic andesite can be explained in terms of fractional crystallization of a parental high-alumina basalt (HAB), which assimilates crustal rocks during its storage, ascent and evolution. Contamination of this melt by Tertiary calc-alkalic intrusives (quartz–diorite and granite, with ⁸⁷Sr/⁸⁶Sr ratios ranging 0.70381–0.70397, nearly identical with those of the Arenal lavas) occurs at upper crustal levels, following the interaction of ascending basaltic magma masses with gabbroic–anorthositic layers. Fragments of these layers are found as inclusions within Arenal lavas and tephra and may show reaction rims (1–5 mm thick, consisting of augite, hypersthene, bytownitic–anorthitic plagioclase, and granular titanomagnetite) at the gabbro–lava interface. These reaction rims indicate that complete `assimilation' was prevented since the temperature of the host basaltic magma was not high enough to melt the gabbroic materials (whose mineral phases are nearly identical to the early formed liquidus phases in the differentiating HAB). Olivine gabbros crystallized at pressure of about 5–6 kbar and equilibrated with the parental HAB at pressures of 3–6 kbar (both under anhydrous and hydrous conditions), and temperatures ranging 1000–1100°C. In particular, `deeper' interactions between the mafic inclusions and the hydrous basaltic melt (i.e., with about 3.5 wt.% H₂O) are likely to occur at 5.4 (±0.4) kbar and temperatures approaching 1100°C. The olivine gabbros are thus interpreted as cumulates which represent crystallized portions of earlier Arenal-type basalts. Some of the gabbros have been `mildly' tectonized and recrystallized to give mafic granulites that may exhibit a distinct foliation. Below Arenal volcano a zoned magma chamber evolved prior the last eruptive cycle: three distinct andesitic magma layers were produced by simple AFC of a high-alumina basalt (HAB) with assimilation of Tertiary quartz–dioritic and granitic rocks. Early erupted 1968 tephra and 1969 lavas (which represent the first two layers of the upper part of a zoned magma chamber) were produced by simple AFC, with fractionation of plagioclase, pyroxene and magnetite and concomitant assimilation of quartz–dioritic rocks. Assimilation rates were constant (r<sub>1</sub>=0.33) for a relative mass of magma remaining of 0.77–0.80, respectively. Lavas erupted around 1974 are less differentiated and represent the `primitive andesitic magma type' residing within the middle–lower part of the chamber. These lavas were also produced by simple AFC: assimilation rates and the relative mass of magma remaining increased of about 10%, respectively (r₁=0.36, and F=0.89). Ba enrichment of the above lavas is related to selective assimilation of Ba from Tertiary granitic rocks. Lava eruption occurred as a dynamic response to the intrusion of a new magma into the old reservoir. This process caused the instability of the zoned magma column inducing syneruptive mixing between portions of two contiguous magma layers (both within the column itself and at lower levels where the new basalt was intruded into the reservoir). Syneruptive mixing (mingling) within the middle–upper part of the chamber involved fractions of earlier gabbroic cumulitic materials (lavas erupted around 1970). On the contrary, within the lower part of the chamber, mixing between the intruded HAB and the residing andesitic melt was followed by simple fractional crystallization (FC) of the hybrid magma layer (lavas erupted in 1978–1980). By that time the original magma chamber was completely evacuated. Lavas erupted in 1982/1984 were thus modelled by means of `open system' AFCRE (i.e., AFC with continuous recharge of a fractionating magma batch during eruption): in this case assimilation rates were r₁=0.33 and F=0.86. Recharge rates are slightly higher than extrusion rates and may reflect differences in density (between extruded and injected magmas), together with dynamic fluctuations of these parameters during eruption. Ba and LREE (La, Ce) enrichments of these lavas can be related to selective assimilation of Tertiary granitic and quartz–dioritic rocks. Calculated contents for Zr, Y and other REE are in acceptable agreement with the observed values. It is concluded that simple AFC occurs between two distinct eruption cycles and is typical of a period of repose or mild and decreasing volcanic activity. On the contrary, magma mixing, eventually followed by fractional crystallization (FC) of the hybrid magma layer, occurs during an ongoing eruption. Open-system AFCRE is only operative when the original magma chamber has been totally replenished by the new basaltic magma, and seems a prelude to the progressive ceasing of a major eruptive cycle.     

Origin of dacites of Taupo Volcanic Zone, New Zealand

Dacites form a relatively small proportion of lavas in the Taupo Volcanic Zone, New Zealand (5km³), and occur mainly on the eastern side. In this paper their origin is considered in terms of three processes: (a) partial melting of crustal rocks; (b) fractional crystallisation of basalt and andesite; and (c) sub-surface mixing of basic and acid magma. Modelling techniques are used to calculate the most acceptable degree of fractional crystallisation and magma mixing to fit major-element data, and these values are used to compare calculated and observed trace-element values. The success or failure of the model is determined by the closeness of the two sets of values. For partial-melt models, trace-element values alone are calculated by the batch-melting equation.Results indicate that White Island dacite can best be modelled by fractional crystallisation; Manawahe by fractional crystallisation plus limited crustal contamination; Maungaongaonga by partial melting of Western Basement greywacke, and Tauhara by partial melting of this greywacke together with minor mixing with a more basic magma. Results from Parekauau and Horohoro indicate that these lavas are unlikely to have formed by any of the processes examined.     

Petrology,geochemistry, and age of the Spurr volcanic complex,eastern Aleutian arc

The Spurr volcanic complex (SVC) is a calc-alkaline, medium-K, sequence of andesites erupted over the last 250000 years by the eastern-most currently active volcanic center in the Aleutian arc. The ancestral Mt. Spurr was built mostly of andesites of uniform composition (58%–60% SiO₂), although andesite production was episodically interrupted by the introduction of new batches of more mafic magma. Near the end of the Pleistocene the ancestral Mt. Spurr underwent avalanche caldera formation, resulting in the production of a volcanic debris avalanche with overlying ashflows. Immediately afterward, a large dome (the present Mt. Spurr) formed in the caldera. Both the ash flows and dome are made of acid andesite more silicic (60%–63% SiO₂) than any analyzed lavas from the ancestral Mt. Spurr, yet contain olivine and amphibole xenocrysts derived from more mafic magma. The mafic magma (53%–57% SiO₂) erupted during and after dome emplacement from a separate vent only 3 km away. Hybrid block-and-ash flows and lavas were also produced. The vents for the silicic and mafic lavas are in the center and in the breach of the 5-by-6-km horseshoe-shaped caldera, respectively, and are less than 4 km apart. Late Holocene eruptive activity is restricted to Crater Peak, and magmas continue to be relatively mafic. SVC lavas are plag ±ol+cpx±opx+mt bearing. All postcaldera units contain small amounts of high-Al₂O₃, high-alkali amphibole, and proto-Crater Peak and Crater Peak lavas contain abundant pyroxenite and anorthosite clots presumably derived from an immediately preexisting magma chamber. Ranges of mineral chemistries within individual samples are often nearly as large as ranges of mineral chemistries throughout the SVC suite, suggesting that magma mixing is common. Elevated Sr, Pb, and O isotope ratios and trace-element systematics incompatible with fractional crystallization suggest that a significant amount of continental crust from the upper plate has been assimilated by SVC magmas during their evolution.     

Magma plumbing system beneath Ontake Volcano, central Japan

Ontake Volcano in central Japan was last active from ~ 100–35 Ka. The eruptions contained rhyodacite pumice and lavas in the first stage (stage O1, > 33 km³), followed by eruptions of andesite lavas and pyroclastics (stages O2 and O3, > 16 km³). Modeling of major and incompatible elements with Sr isotope ratios suggests that the primary magma was a high-alumina basalt. One andesite magma type appears to have evolved from the basalt in a closed system magma chamber, in part by fractional crystallization, and its generation included crustal assimilation. The other andesite magma type is considered to have evolved in an open system magma chamber in which repeated input of primary magma occurred together with wall-rock assimilation and fractional crystallization. The rhyodacite is inferred to have evolved in a closed system magma chamber by fractional crystallization of the second type of andesite. These genetic relationships require that the magma chamber functioned alternately as an open and a closed system. Geobarometry indicates that there may have been multiple magma chambers, located in the upper crust for the rhyodacite, near the upper–lower crust interface for the andesite and in the mid-lower crust for the basalt. These chambers were stacked to form the magma plumbing system of Ontake. Incompatible element compositions of the basalt are considered to have changed during the eruptions, suggesting that two different plumbing systems for stage O1 magma and for stages O2, O3 magmas existed during the 65 Ka of activity. Evolutionary history of the systems implies that the primary magma was introduced into the magma plumbing system each for ~ 17 500 years and that the life span of a magma plumbing system was shorter than 40 Ka.     

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.     

Le magmatisme sursaturé infrabréchique du centre du Cantal (Massif Central français)

Silica oversaturated lavas and pyroclastic flows, 9 to 7,5 M.Y. old, have been emplaced during the sinking of the central volcanotectonic caldera of alkalic stratovolcano Cantal. They can be grouped in a non linear fractional crystallisation series ranging from mugearites to rhyolitic trachytes, comenditic trachytes and comendites through benmoreites. Their evolution results mainly from plagioclase fractionation, alkali feldspar and ferromagnesian minerals playing only a restricted role. We consider this oversaturated group, which follows primordial basanitic lavas in the history of the stratovolcano, as the most evolved liquids resulting from differentiation under high water pressures and oxygen fugacities of alkali basic magmas in a great magma chamber. The less evolved liquids (intermediate and basic) would have been emplaced later, building the greatest part of the volcanic pile.     

Geochemical trends of sequential lava flows from Meseta volcano, Guatemala

The Meseta and Fuego volcanoes closely overlap and collectively are known as the Fuego Volcanic Complex. Historic activity occurs exclusively at Fuego, the southern center, and consists of high-Al basalts. Meseta, the inactive northern center, is predominantly composed of basaltic andesites with minor basalt and andesite. A thick sequence of lava flows and dikes is exposed by a steep collapse escarpment on the east flank of Meseta. The upper 75% of the sequence was sampled from three interfingering stratigraphic sections consisting of 27, 10 and 4 lavas, respectively. Temporal geochemical trends of each section indicates a complex evolutionary history. A major trend toward more evolved compositions upward in the section is consistent with crystal fractionation. This trend is sharply interrupted by the youngest lavas which become distinctly more mafic in composition. Magma mixing is apparently the dominant magmatic evolution process that generated these lavas. The two trends have distinct Sr signatures that suggest a change in parental magma compositions. This abrupt change in composition is interpreted to signal high input rates of mafic magma into the subvolcanic magma chamber. These changes eventually led to sector collapse of Meseta volcano and deposition of the Escuintla debris avalanche. Eruptive activity then migrated to the Fuego volcano where historic activity is similar to that of Meseta immediately prior to its collapse.     

Replenishment of a mafic magma in a zoned felsic magma chamber beneath Rishiri Volcano, Japan

The trachytic Tanetomi lava from Rishiri Volcano, northern Japan, provides useful information concerning how a replenished mafic magma mixes with a compositionally zoned felsic magma in a magma chamber. The Tanetomi lava was erupted in the order of Lower lava 1 (LL1, 59.2-59.8 wt.% in SiO₂), Lower lava 2 (LL2, 58.4-59.1 wt.%), and Upper lava (UL, 59.9-65.1 wt.%). Evidence for mixing with a mafic magma is observed only in the LL2, in which a greater amount of crystals derived from the mafic magma occurs in rocks with higher SiO₂ content. The whole-rock compositional trend of the Tanetomi lavas is fairly smooth except for the LL2 lava composition, which scatter along the main composition trend. There is no reasonable composition of basaltic magma on the extrapolation of the LL2 composition trend, and the trend cannot be explained by a simple two-component magma mixing. Before the replenishment, the felsic magma was zoned in composition (58-65 wt.% in SiO₂) and temperature (1030-920°C) in the magma chamber located at the pressure of ~2 kbar. The compositional variation of the main felsic magma was produced by extraction of a fractionated interstitial melt from mush zones along the chamber walls and its subsequent mixing with the main magma (boundary layer fractionation). The LL1 magma tapped the magma chamber soon after the replenishment, before the mafic magma mixed with the overall felsic magma. Then the basalt magma mixed heterogeneously with the upper part of the felsic magma by forced convection as a fountain during injection. The mixing of the basalt magma with compositionally zoned felsic magma resulted in the characteristic composition trend of the LL2. The fraction of basaltic magma in the LL2 magma is estimated to be at most 10%. Despite such a small proportion, the basalt magma was mixed completely with the felsic magma, probably because the crystallinity of undercooled basalt magma was low enough to behave as a liquid.     

Fluorine and boron geochemistry of an ensialic marginal basin volcano: Deception Island, Bransfield Strait, Antarctica

We present the initial results of a quantitative investigation of the volatile geochemistry of Deception Island, an active volcano situated near the spreading axis of a Quaternary ensialic marginal basin (Bransfield Strait, northern Antarctic Peninsula). Fluorine contents in Deception Island magmas (112–461 ppm) are comparable with lavas from a range of tectonic environments but F-K₂O relationships most closely compare with continental flood basalts and lavas from island arcs and some marginal basins. Boron contents are high (4.3–16.3 ppm) and the values overlap with those of arc lavas; they provide strong support for the presence of a mantle source component derived from the slab subducted at the coeval trench (by melting at the slab/wedge interface and/or during slab dehydration). Both F and B acted incompatibly in Deception Island magmas but there is significant variation in incompatible-element ratios such as K/F, K/B, P/F, P/B, which strongly suggests that the magmatic system was open to some or all of these elements during differentation. The variations in these ratios also provide evidence for the presence of at least two stages in the magmatic evolution of the volcano. During pre-caldera times, mafic magma was emplaced into the upper crust where it evolved and may have reacted with the crustal envelope, thus changing the contents of some or all of the elements F, B, K and P and their inter-element ratios. A later, large influx of hot, mafic magma into the chamber may have been responsible for a major eruption that ultimately led to the formation of the caldera. K/F, K/B, etc, ratios in the magma chamber were “reset” and subsequently continued to change, possibly by further crustal interaction during melt evolution in post-caldera times.     

Petrogenesis of an 800 m lava sequence in eastern Uruguay: insights into magma chamber processes beneath the Paraná flood basalt province

Major and trace element along with representative Sr, Nd and Pb isotope data are presented for drill core samples which intersect an 800 m lava pile in eastern Uruguay. The lavas form part of the Paraná flood basalt province, are low-Ti in composition but distinct from the low-Ti Gramado magma type, and have been termed the Treinte Y Trés magma type. The lava pile overlies a large positive gravity anomaly inferred to reflect an east–west trending, mid-crustal mafic intrusive body with a calculated volume of 35,000 km³. Smooth up-section compositional variations in the basalts are interpreted to record magma evolution within this mid-crustal magma chamber. ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb increase throughout the sequence yet Mg remains relatively constant in the lower 200 m of the sequence, suggesting a role for magma chamber recharge. Above this the lavas show a regular, up-section decrease in Mg coupled with increasing ⁸⁷Sr/⁸⁶Sr and ²⁰⁶Pb/²⁰⁴Pb and this is interpreted to reflect crystal fractionation combined with crustal contamination. The data provide further evidence that contamination of flood basalt magmas in crustal magma chambers is a common phenomenon and calculations suggest that the amount of crustal addition may be as high as 60–70%. Nevertheless, the effects of this crustal contamination do not appear able to account for the discrepancy between key incompatible trace element ratios and isotope ratios of the lavas and those of any putative mantle plume. In fact, La/Ta decreases with decreasing Mg and increasing ⁸⁷Sr/⁸⁶Sr indicating that the effects of crustal contamination were actually to reduce La/Ta and implying that the parental magmas had very high La/Ta (90). These constraints are clearly inconsistent with an asthenospheric origin for the parental magmas and so, consistent with mass balance calculations, it is inferred that they were derived from the lithospheric mantle.     

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.     

Sr and Nd isotope geochemistry of coexisting alkaline magma series,Cantal, Massif Central,France

Sr and Nd isotope analyses are presented for Tertiary continental alkaline volcanics from Cantal, Massif Central, France. The volcanics belong to two main magma series, silica-saturated and silica-undersaturated (with rare nephelinites). Trace element and isotopic data indicate a common source for the basic parental magmas of both major series; the nephelinites in contrast must have been derived from a mantle source which is isotopically and chemically distinct from that which gave rise to the basalts and basanites.⁸⁷Sr/⁸⁶Sr initial ratios range from 0.7034 to 0.7056 in the main magma series (excluding rhyolites) and¹⁴³Nd/¹⁴⁴Nd ratios vary between 0.512927 and 0.512669; both are correlated with increasing SiO₂ in the lavas. The data can be explained by a model of crustal contamination linked with fractional crystallisation. This indicates that crustal magma chambers are the sites of differentiation since only rarely do evolved magmas not show a crustal isotopic signature and conversely basic magmas have primitive isotopic ratios unless they contain obvious crustal-derived xenocrysts. Potential contaminants include lower crustal granulites or partial melts of upper crustal units. Equal amounts of contamination are required for both magma series, refuting hypotheses of selective contamination of the silica-saturated series.The isotopic characteristics of the apparently primary nephelinite lavas demonstrates widespread heterogeneity in the mantle beneath Cantal. Some rhyolites, previously thought to be extremely contaminated or to be crustally derived, are shown to have undergone post-emplacement hydrothermal alteration.     

The origin of intermediate and evolved lavas in the Marquesas archipelago: an example from Nuku Hiva island (French Polynesia)

The Nuku Hiva Pliocene island (Marquesas, French Polynesia) is composed of a large half-collapsed tholeiitic shield volcano (the Tekao edifice), the caldera of which is filled up by the younger Taiohae volcano. The latter edifice is characterised by a complex magmatic association including minor mafic lavas (olivine tholeiites, alkali basalts and basanites), abundant intermediate lavas (hawaiites with subsidiary mugearites, both covering 47% of the surface of the volcano) and lesser amount of evolved lavas (K-rich and Na-rich trachytes and minor benmoreites, covering 25% of the edifice). Most intermediate and evolved Taiohae lavas are amphibole-rich and crystallised under high oxygen fugacities. The mafic Taiohae lavas originated from lower degree of melting of mantle sources more enriched than that of the shield volcano tholeiites. We show that closed-system fractional crystallisation of the Taiohae basaltic magmas can account for the origin of Taiohae hawaiites and mugearites, provided that separation of substantial amount of amphibole and/or apatite occurred during this process. Similarly, fractionation of benmoreitic magmas involving large amounts of amphibole and mica may account for the genesis of K-rich and Na-rich trachytes, respectively. However, fractional crystallisation cannot account for the derivation of benmoreitic magmas from mugearitic ones: since, this process fails to explain the abrupt increase in K₂O from the latter to the former. In addition, the isotopic signature of trachytes and benmoreites is clearly distinct (more EM II-rich) from that of Taiohae basalts, hawaiites and mugearites. Three hypotheses could account for the genesis of benmoreitic magmas: assimilation of oceanic material with a strong EM II signature, differentiation of non-sampled mafic magmas derived from a mantle source having a EM II-rich signature and partial melting at depth of mafic material with a strong EM II signature. The oxidised character of Nuku Hiva lavas, uncommon in oceanic island settings, suggests interaction with water and/or the contribution of an oxidised (altered?) source material to their genesis.     

Volcanological and magmatological evolution of Stromboli volcano (Aeolian Islands): The roles of fractional crystallization,magma mixing,crustal contamination and source heterogeneity

The present paper reports the results of a detailed stratigraphical, petrological and geochemical investigation on the island of Stromboli, Aeolian arc, Southern Tyrrhenian sea. Major and trace element data determined on a large quantity of samples from well-established stratigraphic positions indicate that the magmatological evolution of the island through time was more complex than previously known. The activity of the exposed part of Stromboli, which occurred over a time span of about 100 000 years, started with the emission of high-K calc-alkaline (HKCA) volcanics, which were covered by calc-alkaline (CA), shoshonitic (SHO), high-K calc-alkaline (HKCA) and potassic (KS) products. The most recent activity consists of HKCA lavas and the present-day SHO-basaltic volcanics emitted by mildly explosive “strombolian” activity. Most of the products are lavas, with minor amounts of pyroclastic rocks emplaced mainly during the early stages of activity. The transition from the SHO to the KS cycle was associated with the collapse of the upper part of the volcanic apparatus; the transition from KS to the present-day SHO activity has been found to have occurred at the time of the sliding of the western portion of the volcano that generated the “Sciara del Fuoco” depression. The rock series cropping out at Stromboli show variable enrichment in potassium, incompatible trace elements and radiogenic Sr which increase from CA through HKCA, and SHO up to KS rocks. Major, trace element and Sr-isotopic data agree in indicating that the HKCA and SHO series evolved by crystal/liquid fractionation starting from different parental liquids, whereas crustal assimilation appears to have been the leading process during the evolution of KS volcanics. Mixing processes also played a role although they can be well documented only when they occurred between magmas with different isotopic and geochemical characteristics. Geochemical modelling based on trace element and isotopic data indicates that the mafic magmas of the different volcanic series may be generated by melting of an upper mantle heterogeneously enriched in incompatible elements and radiogenic Sr by addition, via subduction, of different amounts of crustal material. Geochemical data, however, are also in agreement with the alternative hypothesis that the most mafic magmas of the different series have been generated by combined processes of fractional crystallization, assimilation and mixing of a CA magma in a deep-sited magma chamber; the mafic magmas formed by these complex processes were successively emplaced in a shallow reservoir where they evolved by simple fractional crystallization (HKCA and SHO series) and by assimilation of crustal material (KS). The occurrence of changes in the geochemical signatures of the magmas at the time of the structural modification of the volcano is believed to favour the hypothesis that the variable composition observed in the volcanic rocks of Stromboli is the result of processes occurring within the volcanic system.     

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 ascent and eruptive processes from textural and compositional features of Monte Nuovo pyroclastic products, Campi Flegrei, Italy

Geochemical and textural studies were carried out on alkaline products of the AD 1538 Monte Nuovo eruption. Due to the integration of the volcanological study with eyewitness reports, the dynamics and timing of each phase of the eruption and the volume of emitted magmas are known in detail. On this basis, unique in Campi Flegrei, the relations between magma chamber mechanisms, eruptive styles, magma ascent dynamics and volatile exsolution processes have been explored. Glass and phenocryst compositions indicate that the erupted magma has a homogeneous phono-trachytic composition. Textures and compositions of phenocrysts indicate that they crystallised at equilibrium with the melt in the magma chamber, likely as a mushy boundary layer along the chamber wall, where the temperature was below the liquidus temperature of the crystal free-chamber core. The estimated crystallisation temperature is 850±40°C. The magma phase relations in Petrogenys Residua System suggest that phenocryst crystallisation occurred at between 100 and 200 MPa, corresponding to depths ranging from 3 to 8 km. The microlite composition and their close genetic relations with vesicles indicate that groundmass crystallisation occurred during the eruption as a consequence of magma degassing and vesiculation induced by decompression during its ascent toward the surface. Crystal size distributions reveal that microlites grew in two stages of undercooling that we define as: (1) magma migration onset upward from the chamber and (2) magma rising through the conduit to the surface, possibly lasting tens of days and few days, respectively. These results provide information on the physical conditions that characterise pre- and syn-eruptive processes, which may be useful in order to define eruptive scenarios and to evaluate short-term precursors. Furthermore, the collected data provide for the first time information on degassing-induced crystallisation during the eruption of a highly evolved alkaline magma.Editorial responsibility: M. Carroll     

Magma evolution of Quaternary minor volcanic centres in southern Peru,Central Andes

Minor centres in the Central Volcanic Zone (CVZ) of the Andes occur in different places and are essential indicators of magmatic processes leading to formation of composite volcano. The Andahua–Orcopampa and Huambo monogenetic fields are located in a unique tectonic setting, in and along the margins of a deep valley. This valley, oblique to the NW–SE-trend of the CVZ, is located between two composite volcanoes (Nevado Coropuna to the east and Nevado Sabancaya to the west). Structural analysis of these volcanic fields, based on SPOT satellite images, indicates four main groups of faults. These faults may have controlled magma ascent and the distribution of most centres in this deep valley shaped by en-echelon faulting. Morphometric criteria and ¹⁴C age dating attest to four main periods of activity: Late Pleistocene, Early to Middle Holocene, Late Holocene and Historic. The two most interesting features of the cones are the wide compositional range of their lavas (52.1 to 68.1 wt.% SiO₂) and the unusual occurrence of mafic lavas (olivine-rich basaltic andesites and basaltic andesites). Occurrence of such minor volcanic centres and mafic magmas in the CVZ may provide clues about the magma source in southern Peru. Such information is otherwise difficult to obtain because lavas produced by composite volcanoes are affected by shallow processes that strongly mask source signatures. Major, trace, and rare earth elements, as well as Sr-, Nd-, Pb- and O-isotope data obtained on high-K calc-alkaline lavas of the Andahua–Orcopampa and Huambo volcanic province characterise their source and their evolution. These lavas display a range comparable to those of the CVZ composite volcanoes for radiogenic and stable isotopes (⁸⁷Sr/⁸⁶Sr: 0.70591–0.70694, ¹⁴³Nd/¹⁴⁴Nd: 0.512317–0.512509, ²⁰⁶Pb/²⁰⁴Pb: 18.30–18.63, ²⁰⁷Pb/²⁰⁴Pb: 15.57–15.60, ²⁰⁸Pb/²⁰⁴Pb: 38.49–38.64, and δ ¹⁸O: 7.1–10.0‰ SMOW), attesting to involvement of a crustal component. Sediment is absent from the Peru–Chile trench, and hence cannot be the source of such enrichment. Partial melts of the lowermost part of the thick Andean continental crust with a granulitic garnet-bearing residue added to mantle-derived arc magmas in a high-pressure MASH [melting, assimilation, storage and homogenisation] zone may play a major role in magma genesis. This may also explain the chemical characteristics of the Andahua–Orcopampa and Huambo magmas. Fractional crystallisation processes are the main governors of magma evolution for the Andahua–Orcopampa and Huambo volcanic province. An open-system evolution is, however, required to explain some O-isotopes and some major and trace elements values. Modelling of AFC processes suggests the Charcani gneisses and the local Andahua–Orcopampa and Huambo basement may be plausible contaminants.     

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.     

Transitional basalts from the eastern Australian tertiary province

Study of Tertiary volcanic rocks from Mt. Tamborine in S. E. Queensland, Australia, suggests that some basalts from the large Tweed vent are intermediate in character between true tholeiites and well documented alkaline basalts of the Australian Tertiary province. Geochemical evidence and comparison with synthetic systems suggests that the transitional lavas are derived by continuous fractional crystallization during the ascent of a parent magma produced by substantial partial melting of the upper mantle at moderate depths and pressures. Alkaline basalts that underlie the transitional basalts are the result of relatively rapid, intermittent extrusion of magma generated by a smaller degree of partial melting of the upper mantle. This interpretation resolves the difficulties posed by an apparent inversion of the usual stratigraphic relationship of tholeiites capped by alkali basalts, and is in accord with recent seismic studies of the continental margin of eastern Australia.     

Interaction of mantle-derived magma with island crust? Trace element and oxygen isotope data from the Diego Hernandez Formation, Las Cañadas, Tenerife

The Quaternary Diego Hernandez Formation consists of interbedded phonolitic pyroclastics and basanite lavas and scoria beds. Most of the phonolites are mingled-magma units that contain a minor mafic component. The phonolites fall into two stratigraphically bounded groups, based on major and trace element abundances. Nb contents are especially distinctive, due to a varying role for titanite during petrogenesis. Nepheline syenite xenoliths, which are plentiful in some of the phonolitic ignimbrites, fall into the same two compositional groupings but are typically more strongly differentiated. Major and trace element variations during evolution of the phonolites can be modelled by fractional crystallization, by melting of syenite, or by some combination of the two such as AFC. Trace element variations among the basanites require the addition of a highly fractionated felsic component, either phonolitic magma or nepheline syenite. δ¹⁸O values of phonolites vary across twice the range of the basanites, inconsistent with an origin by pure fractional crystallization of a basanitic parent. We conclude that recycling of differentiated rocks within the Tenerife island edifice has played a significant role in Quaternary magmatism on Tenerife.