Crystal retention,fractionation and crustal assimilation in a convecting magma chamber,Nisyros Volcano,Greece

Nisyros island is a calc-alkaline volcano, built up during the last 100 ka. The first cycle of its subaerial history includes the cone-building activity with three phases, each characterized by a similar sequence: (1) effusive and explosive activity fed by basaltic andesitic and andesitic magmas; and (2) effusive andextrusive activity fed by dacitic and rhyolitic magmas. The second eruptive cycle includes the caldera-forming explosive activity with two phases, each consisting of the sequence: (1) rhyolitic phreatomagmatic eruptions triggering a central caldera collapse; and (2) extrusion of dacitic-rhyolitic domes and lava flows. The rocks of this cycle are characteized by the presence of mafic enclaves with different petrographic and chemical features which testify to mixing-mingling processes between variously evolved magmas. Jumps in the degree of evolution are present in the stratigraphic series, accompanied by changes in the porphyritic index. This index ranges from 60% to about 5% and correlates with several teochemical parameters, including a negative correlation with Sr isotope ratios (0.703384–0.705120). The latter increase from basaltic andesites to intermediate rocks, but then slightly decrease in the most evolved volcanic rocks. The petrographic, geochemical and isotopic characteristics can be largely explained by processes occurring in a convecting, crystallizing and assimilating magma chamber, where crystal sorting, retention, resorption and accumulation take place. A group of crystal-rich basaltic andesites with high Sr and compatible element contents and low incompatible elements and Sr isotope ratios probably resulted from the accumulation of plagioclase and pyroxene in an andesitic liquid. Re-entrainment of plagioclase crystals in the crystallizing magma may have been responsible for the lower ⁸⁷Sr/⁸⁶Sr in the most evolved rocks. The gaps in the degree of evolution with time are interpreted as due to liquid segregation from a crystal mush once critical crystallinity was reached. At that stage convection halted, and a less dense, less porphyritic, more evolved magma separated from a denser crystal-rich magma portion. The differences in incompatible element enrichment of pre-and post-caldera dacites and the chemical variation in the post-caldera dome sequence are the result of hybridization of post-caldera dome magmas with more mafic magmas, as represented by the enclave compositions. The occurrence of the quenched, more mafic magmas in the two post-caldera units suggests that renewed intrusion of mafic magma took place after each collapse event.     

Bimodal volcanism at the Katla subglacial caldera,Iceland: insight into the geochemistry and petrogenesis of rhyolitic magmas

The Katla subglacial caldera is one of the most active and hazardous volcanic centres in Iceland as revealed by its historical volcanic activity and recent seismic unrest and magma accumulation. A petrologic and geochemical study was carried out on a suite of mid-Pleistocene to Recent lavas and pyroclastic rocks originated from the caldera. The whole series is characterised by a bimodal composition, including Fe-Ti transitional alkali basalts and mildly alkalic rhyolites. Variations in trace-element composition amongst the basalts and rhyolites show that their chemical differentiation was mainly controlled by fractional crystallisation and possible assimilation. The petrology and chemistry of the few intermediate extrusive rocks show that they were derived from magma mingling or hybridisation. The absence of extrusive rocks of true intermediate magmatic composition and the occurrence of amphibole-bearing felsic xenoliths support the hypothesis of partial melting of the hydrated basalt crust as the main process leading to the generation of rhyolites. The ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr values of Katla volcanic rocks fit the general isotopic array defined by late Quaternary to Recent lavas from Iceland. A few rock specimens are distinguished by low ¹⁴³Nd/¹⁴⁴Nd values suggesting assimilation and mixing of much older crustal material. Despite their similar whole-rock chemical compositions, the postglacial rhyolitic extrusives differ from the felsic xenoliths by their glass composition and the absence of amphibole. This, together with the general chemical trend of volcanic glasses, indicates that the postglacial rhyolitic extrusives were probably derived by a process involving late reheating and partial melting of crustal material by intrusion of basaltic magmas.     

Sr–Nd isotopic and chemical characteristics of the silicic magma reservoir of the Aira pyroclastic eruption, southern Kyushu, Japan

Sr and Nd isotope and geochemical investigations were performed on a remarkably homogeneous, high-silica rhyolite magma reservoir of the Aira pyroclastic eruption (22,000 years ago), southern Kyushu, Japan. The Aira caldera was formed by this eruption with four flow units (Osumi pumice fall, Tsumaya pryoclastic flow, Kamewarizaka breccia and Ito pyroclastic flow). Quite narrow chemical compositions (e.g., 74.0–76.5 wt% of SiO₂) and Sr and Nd isotopic values (⁸⁷Sr/⁸⁶Sr=0.70584–0.70599 and _Nd=−5.62 to −4.10) were detected for silicic pumices from the four units, with the exception of minor amounts of dark pumices in the units. The high Sr isotope ratios (0.7065–0.7076) for the dark pumices clearly suggest a different origin from the silicic pumices. Andesite to basalt lavas in pre-caldera (0.37–0.93 Ma) and post-caldera (historical) eruptions show lower ⁸⁷Sr/⁸⁶Sr (0.70465–0.70540) and higher _Nd (−1.03 to +0.96) values than those of the Aira silicic and dark pumices. Both andesites of pre- and post-caldera stages are very similar in major- and trace-element characteristics and isotope ratios, suggesting that the both andesites had a same source and experienced the same process of magma generation (magma mixing between basaltic and dacitic magmas). Elemental and isotopic signatures deny direct genetic relationships between the Aira pumices and pre- and post-caldera lavas. Relatively upper levels of crust (middle–upper crust) are assumed to have been involved for magma generation for the Aira silicic and dark pumices. The Aira silicic magma was derived by partial melting of a separate crust which had homogeneous chemistry and limited isotope compositions, while the magma for the Aira dark pumice was generated by AFC mixing process between the basement sedimentary rocks and basaltic parental magma, or by partial melting of crustal materials which underlay the basement sediments. The silicic magma did not occupy an upper part of a large magma body with strong compositional zonation, but formed an independent magma body within the crust. The input and mixing of the magma for dark pumices to the base of the Aira silicic magma reservoir might trigger the eruptions in the upper part of the magma body and could produce a slight Sr isotope gradient in the reservoir. An extremely high thermal structure within the crust, which was caused by the uprise and accumulation of the basaltic magma, is presumed to have formed the large volume of silicic magma of the Aira stage.     

Eruptive history and petrology of Mount Drum volcano,Wrangell Mountains,Alaska

Mount Drum is one of the youngest volcanoes in the subduction-related Wrangell volcanic field (80×200 km) of southcentral Alaska. It lies at the northwest end of a series of large, andesite-dominated shield volcanoes that show a northwesterly progression of age from 26 Ma near the Alaska-Yukon border to about 0.2 Ma at Mount Drum. The volcano was constructed between 750 and 250 ka during at least two cycles of cone building and ring-dome emplacement and was partially destroyed by violent explosive activity probably after 250 ka. Cone lavas range from basaltic andesite to dacite in composition; ring-domes are dacite to rhyolite. The last constructional activity occurred in the vicinity of Snider Peak, on the south flank of the volcano, where extensive dacite flows and a dacite dome erupted at about 250 ka. The climactic explosive eruption, that destroyed the top and a part of the south flank of the volcano, produced more than 7 km³ of proximal hot and cold avalanche deposits and distal mudflows. The Mount Drum rocks have medium-K, calc-alkaline affinities and are generally plagioclase phyric. Silica contents range from 55.8 to 74.0 wt%, with a compositional gap between 66.8 and 72.8 wt%. All the rocks are enriched in alkali elements and depleted in Ta relative to the LREE, typical of volcanic arc rocks, but have higher MgO contents at a given SiO₂, than typical orogenic medium-K andesites. Strontium-isotope ratios vary from 0.70292 to 0.70353. The compositional range of Mount Drum lavas is best explained by a combination of diverse parental magmas, magma mixing, and fractionation. The small, but significant, range in ⁸⁷Sr/⁸⁶Sr ratios in the basaltic andesites and the wide range of incompatible-element ratios exhibited by the basaltic andesites and andesites suggests the presence of compositionally diverse parent magmas. The lavas show abundant petrographic evidence of magma mixing, such as bimodal phenocryst size, resorbed phenocrysts, reaction rims, and disequilibrium mineral assemblages. In addition, some dacites and andesites contain Mg and Ni-rich olivines and/or have high MgO, Cr, Ni, Co, and Sc contents that are not in equilibrium with the host rock and indicate mixing between basalt or cumulate material and more evolved magmas. Incompatible element variations suggest that fractionation is responsible for some of the compositional range between basaltic andesite and dacite, but the rhyolites have K, Ba, Th, and Rb contents that are too low for the magmas to be generated by fractionation of the intermediate rocks. Limited Sr-isotope data support the possibility that the rhyolites may be partial melts of underlying volcanic rocks. Received March 13, 1993/Accepted September 10, 1993     

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

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

Subaqueous volcanism in the Paleo-Pacific Ocean based on Jurassic basaltic tuff and pillow basalt in the Raohe Complex,NE China

On-land records of subaqueous explosive volcanic eruptions are rarely reported.To understand this phenomenon and discuss its global significance,we studied the geochronology and geochemistry of basaltic tuff and pillow basalt in the Raohe Complex,NE China.The basaltic tuff consists of well-sorted vitreous,crystal(mostly clinopyroxene),and minor lithic fragments.It is characterized by a high Mg O(15.7–15.9%)content and zero Eu anomalies(Eu/Eu~*=99–102).The tuff erupted at 172±1 Ma based on SHRIMP zircon U-Pb dating,coeval with the previously reported age of the pillow basalt.The pillow basalt has intermediate Mg O content and weakly negative Eu anomalies(Eu/Eu~*=90–99).Based on immobile trace element discrimination,the basaltic tuff and pillow basalt belong to alkali basalt displaying an OIB-type trace element pattern,and consistent Nd isotope signatures ofε_(Nd)(t)=4.4–6.2,indicating an identical mantle source.The pillow basalt has coupled Sr-Nd isotopic values,whereas the basaltic tuff has significantly higher initial~(87)Sr/~(86)Sr values that are similar to synchronous seawater.This indicates that the elemental exchange between the mantle-derived material and seawater most likely occurred in a subaqueous explosive volcanic eruption,rather than in an effusive eruption.Detailed calculations suggest that the high efficiency of the Sr-isotope exchange between seawater and the mantle-derived material triggered by a subaqueous explosive volcanic eruption is likely one of the main reasons for the rapid decrease of the global seawater~(87)Sr/~(86)Sr value.     

Petrogenesis of orthopyroxene- and amphibole-bearing andesites, Mustique, Grenadine Islands, Lesser Antilles Arc: Isotope, trace element and physical constraints

Abstract On the island of Mustique, fresh and propylitized olivine–plagioclase–clinopyroxene basalt, plagioclase–clinopyroxene–orthopyroxene and plagioclase–clinopyroxene–amphibole andesite lavas and minor intrusions are interbedded with Oligocene pyroclastic and epiclastic rocks. Chemical data show that two isotopically identical, but chemically different, suites of lava are present: (i) the OPXS (⁸⁷Sr/⁸⁶Sr 0.70403–0.70454; ¹⁴³Nd/¹⁴⁴Nd 0.512952–0.512986; δ¹⁸O_cpx 5.49 and 5.61), comprising basalts and orthopyroxene‐bearing andesites; and (ii) the AMPHS (⁸⁷Sr/⁸⁶Sr 0.70401–0.70457; ¹⁴³Nd/¹⁴⁴Nd 0.512981–0.513037; δ¹⁸O_cpx 5.54), made up of basalts and amphibole‐bearing andesites. The OPXS has higher contents of TiO₂, P₂O₅, light rare earth elements, Sm, Pb, Th, U, Zr, Y and Nb, and higher La/Yb ratios than the AMPHS. The isotopic data suggest that both suites formed from melts derived from the same subduction‐modified depleted mantle source as the volcanic rocks of nearby St Vincent and Bequia, and the northern islands of the Lesser Antilles Arc. The immobile trace element contents, and La/Yb ratios, of the OPXS are indicative of ～10% partial melting of the source, whereas those of the AMPHS are indicative of ～25% partial melting. The within‐suite chemical variation of the OPXS is consistent with ～45% fractional crystallization of its intratelluric mineral assemblages, and that of the AMPHS is consistent with the removal of ～65% of its intratelluric assemblages. Experimental evidence suggests that both suites of basalt crystallized at pressures <8 kbar from melts containing 1–2 wt% water. After extensive fractional crystallization, the andesites crystallized at pressures between approximately 5 and 2 kbar. The OPXS magmas appear to have lost more of their water content than the AMPHS magmas. Thus, the OPXS andesites formed from melts with an estimated water content of 2–3 wt%, whereas the AMPHS andesites formed from melts containing at least 4.5 wt% water.     

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 approach to magmatic evolution of Mt. Erciyes stratovolcano Central Anatolia, Turkey

Erciyes stratovolcano, culminating at 3917 m, is located in the Cappadocian region of central Anatolia. During its evolution, this Quaternary volcano produced pyroclastic deposits and lava flows. The great majority of these products are calc-alkaline in character and they constitute Kocdag and Erciyes sequences by repeated activities. Alkaline activity is mainly observed in the first stages of Kocdag and approximately first-middle stages of Erciyes sequences. Generally, Kocdag and Erciyes stages terminate by pyroclastic activities. The composition of lavas ranges from basalt to rhyolite (48.4–70.5 wt.% SiO₂). Calc-alkaline rocks are represented mostly by andesites and dacites. Some compositional differences between alkaline basaltic, basaltic and andesitic rocks were found; while the composition of dacites remain unchanged. All these volcanics are generally enriched in LIL and HFS elements relative to the orogenic values except Rb, Ba, Nb depleted alkaline basalt. ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd isotopic composition of the volcanics range between 0.703344–0.703964, 0.512920–0.512780 for alkaline basalts and change between 0.704322–0.705088, 0.512731–0.512630 for alkaline basaltic rocks whereas calc-alkaline rocks have relatively high Sr and Nd isotopic ratios (0.703434–0.705468, 0.512942–0.512600). Low Rb, Ba, Nb content with high Zr/Nb, low Ba/Nb, La/Yb ratio and low Sr isotopic composition suggest an depleted source component, while high Ba, Rb, Nb content with high La/Yb, Ba/Nb, low Zr/Nb and low ⁸⁷Sr/⁸⁶Sr ratios indicate an OIB-like mantle source for the generation of Erciyes alkaline magma. These elemental and ratio variations also indicate that the different mantle sources have undergone different degree of partial melting episodes. The depletion in Ba, Rb, Nb content may be explained by the removal of these elements from the source by slab-derived fluids which were released from pre-collisional subduction, modified the asthenospheric mantle. The chemically different mantle sources interacted with crustal materials to produce calc-alkaline magma. The Ba/Nb increase of calc-alkaline samples indicates the increasing input of crustal components to Erciyes volcanics. Sr and Nd isotopic compositions and elevated LIL and HFS element content imply that calc-alkaline magma may be derived from mixing of an OIB-like mantle melts with a subduction-modified asthenospheric mantle and involvement of crustal materials in intraplate environments.     

Genesis of lavas of the Taupo Volcanic Zone, North Island, New Zealand

The Taupo Volcanic Zone forms part of the Taupo-Hikurangi subduction system, and comprises five volcanic centres: Tongariro, Taupo, Maroa, Okataina and Rotorua. Tongariro Volcanic Centre is formed almost entirely of andesite while the other four centres contain predominantly rhyolitic volcanics and later fissure eruptions of high-Al basalt. Estimated total volume of each lava type are as follows: 2 km³ of high-Al basalt (< 0.1%); 260 km³ of andesite (< 2.5%); 5 km³ of dacite (< 0.1%); > 10,000 km³ of rhyolite and ignimbrite (> 97.4%).The location of the andesites and vent alignments suggest a source from a subduction zone underlying the area. However, the lavas differ chemically from island-arc andesites such as those of Tonga; in particular by having higher contents of the alkali elements, light REE and Sr and Pb isotopes. This suggests some crustal contamination, and it is considered that this may occur beneath the wide accretionary prism of the subduction system. Amphibolite of the subduction zone will break down between 80 and 100 km and a partial melt will rise. A multi-stage process of magma genesis is then likely to occur. High-Al basalts are thought to be derived from partial melting of a garnet-free peridotite near the top of the mantle wedge overlying the subduction zone, locations of the vents controlled largely by faults within the crust. Rhyolites and ignimbrites were probably derived from partial melting of Mesozoic greywacke and argillite under the Taupo Volcanic Zone. Initial partial melting may have been due to hydration of the base of the crust; the “water” having come from dehydration of the downgoing slab. The partial melts would rise to form granodiorite plutons and final release of the magma to form rhyolites and ignimbrites was allowed because of extension within the Taupo graben.Dacites of the Bay of Plenty probably resulted from mixing of andesitic magma with small amounts of rhyolitic magma, but those on the eastern side of the Rotorua-Taupo area were more likely formed by a higher degree of partial melting of the Mesozoic greywacke-argillite basement. This may be due to intrusion of andesite magma on this side of the Taupo volcanic zone.     

Relations of cinder cones to the magmatic evolution of Mount Mazama,Crater Lake National Park,Oregon

Cinder cones at Crater Lake are composed of high-alumina basaltic to andesitic scoria and lavas. The Williams Crater Complex, a basaltic cinder cone with andesitic to dacitic lava flows, stands on the western edge of the caldera, against an andesite flow from Mount Mazama. Bombs erupted from Williams Crater contain cores of banded andesite and dacite, similar to those erupted during the climatic eruption of Mount Mazama.Major- and trace-element variations exhibit an increase in incompatible elements and a decrease in compatible elements, consistent with crystal fractionation of olivine, plagioclase, clinopyroxene, orthopyroxene, and magnetite. LREE patterns in the rocks are irregular; each successive basalt is enriched in LREE relative to the preceding andesite.Compositional variations in the magmas of the cinder cones suggest that three magmatic processes were involved, partial melting, fractional crystallization, and magma mixing. Partial melting of more than one source produced primary basaltic magma(s). Subsequent mixing and fractional crystallization produced the more differentiated basaltic to andesitic magmas.     

Setouchi high-Mg andesites revisited: geochemical evidence for melting of subducting sediments

In order to evaluate the mechanism of production of unusual high-Mg andesite (HMA) magmas, Pb–Nd–Sr isotopic compositions were determined for HMAs and basalts from the Miocene Setouchi volcanic belt in the SW Japan arc. The isotopic compositions of Setouchi rocks form mixing lines between local oceanic sediments and Japan Sea backarc basin basalts, suggesting a significant contribution of the subducting sediment component to the HMA magma generation. Mixing calculations using compositions of an inferred original mantle and local oceanic sediments suggest that a sediment-derived melt, neither an H₂O-rich fluid nor an amphibolite/eclogite-derived melt, could have been produced first and served as a plausible metasomatic agent for the HMA magma source. The unusual tectonic setting, including subduction of a newly-borne hence hot plate, may be responsible for melting of subducting sediments.     

Evolution and geodynamic significance of the tertiary orogenic volcanism in Northeastern Greece

The Tertiary volcanism of Eastern Macedonia and Western Thrace (Greece) developed in association with the sedimentary basin which formed, from Eocene to Oligocene, along the southern margin of the Rhodope Massif.The volcanic products, ranging in composition from basaltic andesites to rhyolites, show an overall calc-alkaline orogenic affinity, while chemical characteristics identify different groups of rocks, probably reflecting minor differences among parent magmas. The observed evolution within any group of rocks is compatible with fractional crystallization processes acting on relatively shallow magma bodies.The Sr isotopic composition of rhyolitic member shows an initial⁸⁷Sr/⁸⁶Sr ratio comparable with that of basaltic andesites, reinforcing the hypothesis of a crystal/liquid line of descent.Geochemical and petrographic evidence, on the whole, suggests that the investigated orogenic association developed on an active continental margin characterized by a relatively thick crust, acting as a density filter for the basic magmas and facilitating their storage and fractionation within the crust itself. Minor contamination by interaction with host materials may also have occurred.Stratigraphic and K/Ar geochronological data indicate that the volcanic activity started in Upper Eocene and reached its maximum development in Upper Oligocene. From Lower Miocene, the volcanism shifted southward in the Central Aegean area and in part of Western Anatolia, coming to an end by Middle Miocene.The southward migration of the volcanic front has been interpreted as a consequence of the increase in the dipping of the Benioff zone, due to the decrease of penetrative strength after the main phase of continental collision.     

Geochemistry, strontium isotope data, and potassium-argon ages of the andesite-rhyolite association in the Padang area, West Sumatra

Quaternary volcanoes in the Padang area on the west coast of Sumatra have produced two-pyroxene, calc-alkaline andesite and volumetrically subordinate rhyolitic and andesitic ash-flow tuffs. A sequence of andesite (pre-caldera), rhyolitic tuff and andesitic tuff, in decreasing order of age, is related to Maninjau caldera. Andesite compositions range from 55.0 to 61.2% SiO₂ and from 1.13 to 2.05% K₂O. Six K-Ar whole-rock age determinations on andesites show a range of 0.27 ± 0.12 to 0.83 ± 0.42 m.y.; a single determination on the rhyolitic ashflow tuff gave 0.28 ± 0.12 m.y.Eight ⁵⁷Sr/²⁶Sr ratios on andesites and rhyolite tuff west of the Semangko fault zone are in the range 0.7056 – 0.7066. These ratios are higher than those elsewhere in the Sunda arc but are comparable to the Taupo volcanic zone of New Zealand and calc-alkaline volcanics of continental margins. An ⁸⁷Sr/⁸⁶Sr ratio of 0.7048 on G. Sirabungan east of the Semangko fault is similar to an earlier determination on nearby G. Marapi (0.7047), and agrees with ⁸⁷Sr/⁸⁶Sr ratios in the rest of the Sunda arc. The reason for this distribution of ⁸⁷Sr/⁸⁶Sr ratios is unknown.The high ⁸⁷Sr/⁸⁶Sr ratios are tentatively regarded to reflect a crustal source for the andesites, while moderately fractionated REE patterns with pronounced negative Eu anomalies suggest a residue enriched in plagioclase with hornblende and/or pyroxenes. Generation of associated andesite and rhyolite could have been caused by hydrous fractional melting of andesite or volcanogenic sediments under adiabatic decompression.     

The volcanic and magmatic evolution of Volcán Ollagüe, a high-K, late quaternary stratovolcano in the Andean Central Volcanic Zone

Volcán Ollagüe is a high-K, calc-alkaline composite volcano constructed upon extremely thick crust in the Andean Central Volcanic Zone. Volcanic activity commenced with the construction of an andesitic to dacitic composite cone composed of numerous lava flows and pyroclastic deposits of the Vinta Loma series and an overlying coalescing dome and coulée sequence of the Chasca Orkho series. Following cone construction, the upper western flank of Ollagüe collapsed toward the west leaving a collapse-amphitheater about 3.5 km in diameter and a debris avalanche deposit on the lower western flank of the volcano. The deposit is similar to the debris avalanche deposit produced during the May 18, 1980 eruption of Mount St. Helens, U.S.A., and was probably formed in a similar manner. It presently covers an area of 100 km² and extends 16 km from the summit. Subsequent to the collapse event, the upper western flank was reformed via eruption of several small andesitic lava flows from vents located near the western summit and growth of an andesitic dome within the collapse-amphitheater. Additional post-collapse activity included construction of a dacitic dome and coulée of the La Celosa series on the northwest flank. Field relations indicate that vents for the Vinta Loma and post-collapse series were located at or near the summit of the cone. The Vinta Loma series is characterized by an anhydrous, two-pyroxene assemblage. Vents for the La Celosa and Chasca Orkho series are located on the flanks and strike N55 W, radial to the volcano. The pattern of flank eruptions coincides with the distribution in the abundance of amphibole and biotite as the main mafic phenocryst phases in the rocks. A possible explanation for this coincidence is that an unexposed fracture or fault beneath the volcano served as a conduit for both magma ascent and groundwater circulation. In addition to the lava flows at Ollagüe, magmas are also present as blobs of vesiculated basaltic andesite and mafic andesite that occur as inclusions in nearly all of the lavas. All eruptive activity at Ollagüe predates the last glacial episode ( 11.000 a B.P.), because post-collapse lava flows are overlain by moraine and are incised by glacial valleys. Present activity is restricted to emission of a persistent, 100-m-high fumarolic steam plume from a vent located within the summit andesite dome.Sr and Nd isotope ratios for the basaltic andesite and mafic andesite inclusions and lavas suggest that they have assimilated large amounts of crust during crystal fractionation. In contrast, narrow ranges in ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr in the andesitic and dacitic lavas are enigmatic with respect to crustal contamination.     

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

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

An outline of the geology and geochemistry,and the possible petrogenetic evolution of the volcanic rocks of the Tonga-Kermadec-New Zealand island arc

The Pleistocene-Recent volcanism of this arc extends nearly linearly NNE from northern New Zealand for some 2800 km. Along its western margin lies an active marginal basin (Lau Basin and Havre Trough) which has its southern termination in the Taupo volcanic zone (TVZ, New Zealand). The New Zealand arc segment is developed within a continental crust, whereas the Tonga-Kermadec segments are developed on a ridge system within the oceanic basin. Submarine morphology suggests that the Kermadec volcanoes represent a less advanced stage of evolution relative to those of Tonga.Magmas erupted within the TVZ are dominantly rhyolitic (≈16,000 km³) with subordinate andesites and rare high-alumina tholeiites and dacites. The Kermadec Islands are dominated by tholeiites and basaltic andesites, with subordinate andesites and dacites. The Tongan Islands are dominated by basaltic andesites, with locally developed andesites and dacites. These Tonga-Kermadec lavas are characterised by subcalcic groundmass clinopyroxenes, whereas the younger group of TVZ andesites contain groundmass hypersthene and augite.Geochemically, the TVZ andesites are systematically enriched (relative to those of Tonga-Kermadec) in “incompatible” elements (e.g. K, Rb, Cs, Ba, light REE, U, Th, Zr, Pb), are less Fe-enriched, and contain more radiogenic Sr and Pb (excepting certain ²⁰⁷Pb/²⁰⁴Pb compositions). The evidence points to crustal equilibration of the TVZ andesites prior to eruption.A complete overlap of major and trace element chemistry (including TiO₂) is observed between the Kermadec-TVZ tholeiites and basaltic andesites, and the ocean floor tholeiites of the Lau Basin. Compared to the Tongan lavas, those of the Kermadecs exhibit a greater degree of chemical variability, also reflected in the greater heterogeneity in their Pb isotopic compositions. Moreover, many of the Tonga-Kermadec basaltic andesites exhibit more depleted “incompatible” trace element abundances than the Kermadec and TVZ tholeiites.The “primary” magmas of this arc are interpreted to be of basaltic andesite type, derived from Benioff zone melting (essentially anhydrous), but extensively modified by low-pressure crystal fractionation processes. The Kermadec tholeiites are explained as products of relatively shallow upper mantle partial fusion induced during the earlier stages of diapiric rise of Benioff zone-derived magmas, which are sufficiently hot to intersect the peridotite solidus. This should result in the production and intermixing of a series of magmas extending from olivine tholeiite to basaltic andesite composition. The voluminous rhyolites of TVZ are interpreted as the products of crustal fusion involving Mesozoic sediments.     

Magmatic evolution of Pacaya and Cerro Chiquito volcanological complex,Guatemala

Four major phases are distinguished during the building of the Pacaya volcanological complex (Guatemala): (1) the ancestral volcano, now much eroded, covered by younger deposits and battered by faulting and landslides; (2) the initial cone made up of large lava flows and dated at about 0.5 Ma; (3) andesito-dacitic domes (Cerro Chiquito dome and others) emplaced during an extrusive phase at about 0.16 Ma; and (4) the active Pacaya volcano. Lavas of phases 2 and 4 are basalts and basaltic andesites with almost the same major and trace element compositions. Classical enrichment in LILE and depletion in HFSE are observed. Phase 3 domes show magma-mingling features. The dacitic host rock includes basaltic andestic enclaves, 20 to 30% in volume. According to geochemical and mineralogic data (Mg/Fe ratios of basic minerals higher in dacite, groundmass glasses sodic in dacite and potassic in basaltic andesite), the basaltic andesites and dacites of phase 3 cannot be related by a simple fractional crystallization process. The existence of such differences suggests that magma mingling/mixing processes were involved by a connection between the two magma chambers prior to the extrusion of the andesito-dacitic domes. However, some trace element data clearly suggest that fractional crystallization played a significant role in the differentiation of these lavas. Remelting of amphibole-bearing cumulates from the dacite may also have played a role in the basaltic andesitic liquid genesis. Thermodynamical parameters of each liquid are contrasted. The basaltic andesitic magma, at a high temperature (1037°C) and in relatively small amounts, is embayed in the cooler (905° C) dacitic magma. The former liquid, denser (2.72) and less viscous (10^3.31 poises for free crystal liquid) may crystallize while the latter, lighter (2.60) and more viscous (10^4.46 poises), remains still liquid. Isotopic data (0.70383<⁸⁷Sr/⁸⁶Sr <0.70400; 0.512785<¹⁴³Nd/¹⁴⁴Nd<0.512908; 18.61<²⁰⁶Pb/²⁰⁴Pb<18.66; 15.56<²⁰⁷Pb/²⁰⁴Pb <15.58; 38.30<²⁰⁸Pb/²⁰⁴Pb<38.40) indicate that all the lavas (from Pacaya as well as from Cerro Chiquito) are cogenetic and derive from the same mantle source. Sr, Nd and Pb isotope ratios are similar to those of OIBs. (²³⁰Th/²³²Th) activity ratios on two historical lavas are respectively 1.2 and 1.3. The Th excess is similar to that of other calcalkaline volcanoes emplaced on a continental crust. These lavas evolved, possibly in separate magma chambers, through processes of fractional crystallization and magma mixing.     

Early Jurassic intra‐oceanic arc system of the Neotethys Ocean: Constraints from andesites in the Gangdese magmatic belt,south Tibet

The Gangdese magmatic belt is located in the southern margin of the Lhasa terrane, south Tibet. Here zircon U–Pb ages and Hf isotopic data, as well as whole‐rock geochemistry and Sr–Nd isotopes on andesites from the Bima Formation with a view to evaluating the history of the Gangdese magmatism and the evolution of the Neotethys Ocean. Zircon U–Pb dating yields an age of ca 170 Ma from six samples, representing the eruptive time of these volcanic rocks. Zircon Hf isotopes show highly positive ε_Hf(t) values of +13 to +16 with a mean of +15.2. Whole‐rock geochemical and Sr–Nd isotopic results suggest that the magma source of these andesites was controlled by partial melting of a depleted mantle source with addition of continental‐derived sediments, similar to those in the southern arcs of the Lesser Antilles arc belt. In combination with published data, the volcanic rocks of the Bima Formation are proposed to have been generated in an intra‐oceanic arc system, closely associated with northward subduction of the Neotethyan oceanic lithosphere.     

The eruptive history of the Tequila volcanic field, western Mexico: ages, volumes, and relative proportions of lava types

The eruptive history of the Tequila volcanic field (1600 km²) in the western Trans-Mexican Volcanic Belt is based on ⁴⁰Ar/³⁹Ar chronology and volume estimates for eruptive units younger than 1 Ma. Ages are reported for 49 volcanic units, including Volcán Tequila (an andesitic stratovolcano) and peripheral domes, flows, and scoria cones. Volumes of volcanic units 1 Ma were obtained with the aid of field mapping, ortho aerial photographs, digital elevation models (DEMs), and ArcGIS software. Between 1120 and 200 kyrs ago, a bimodal distribution of rhyolite (~35 km³) and high-Ti basalt (~39 km³) dominated the volcanic field. Between 685 and 225 kyrs ago, less than 3 km³ of andesite and dacite erupted from more than 15 isolated vents; these lavas are crystal-poor and show little evidence of storage in an upper crustal chamber. Approximately 200 kyr ago, ~31 km³ of andesite erupted to form the stratocone of Volcán Tequila. The phenocryst assemblage of these lavas suggests storage within a chamber at ~2–3 km depth. After a hiatus of ~110 kyrs, ~15 km³ of andesite erupted along the W and SE flanks of Volcán Tequila at ~90 ka, most likely from a second, discrete magma chamber located at ~5–6 km depth. The youngest volcanic feature (~60 ka) is the small andesitic volcano Cerro Tomasillo (~2 km³). Over the last 1 Myr, a total of 128±22 km³ of lava erupted in the Tequila volcanic field, leading to an average eruption rate of ~0.13 km³/kyr. This volume erupted over ~1600 km², leading to an average lava accumulation rate of ~8 cm/kyr. The relative proportions of lava types are ~22–43% basalt, ~0.4–1% basaltic andesite, ~29–54% andesite, ~2–3% dacite, and ~18–40% rhyolite. On the basis of eruptive sequence, proportions of lava types, phenocryst assemblages, textures, and chemical composition, the lavas do not reflect the differentiation of a single (or only a few) parental liquids in a long-lived magma chamber. The rhyolites are geochemically diverse and were likely formed by episodic partial melting of upper crustal rocks in response to emplacement of basalts. There are no examples of mingled rhyolitic and basaltic magmas. Whatever mechanism is invoked to explain the generation of andesite at the Tequila volcanic field, it must be consistent with a dominantly bimodal distribution of high-Ti basalt and rhyolite for an 800 kyr interval beginning ~1 Ma, which abruptly switched to punctuated bursts of predominantly andesitic volcanism over the last 200 kyrs.Electronic Supplementary Material Supplementary material is available in the online version of this article at Editorial responsility: J. Donnelly-NolanThis revised version was published online in January 2005 with corrections to Tables 1 and 3.An erratum to this article can be found at