Nd-Sr systematics of the Setouchi volcanic rocks,southwest Japan: a clue to the origin of orogenic andesite

Twenty-three volcanic rocks from the Setouchi volcanic belt, southwest Japan, were analyzed for Nd and Sr isotopic compositions for the purpose of examining the genetic relationships among the basalt, high-magnesium andesite (HMA) and evolved porphyritic andesite. The andesites have higher⁸⁷Sr/⁸⁶Sr (0.70487–0.70537) and lower¹⁴³Nd/¹⁴⁴Nd (0.512509–0.512731) than the basalts, i.e., 0.70408–0.70468 and 0.512691–0.512830, respectively. This result confirms earlier conclusions obtained from petrologic study that the andesites cannot be fractionation products of basaltic magma but that the andesitic and basaltic magmas were generated independently. On the basis of melting experiments for HMA and basalt, it is inferred that there is an isotopically stratified mantle beneath southwest Japan. Evolved porphyritic andesites have essentially identical Sr and Nd isotopic ratios to HMA and can be derived by fractionation of primary andesitic magma. A model to produce orogenic andesite is proposed on petrologic, experimental and isotopic bases.     

Rare earth and strontium isotope evidence concerning the petrogenesis of North Chilean ignimbrites

New rare earth element (REE) data, Rb and Sr analyses and Sr isotope measurements are presented for pumice clasts collected from some North Chilean ignimbrites of dacite and rhyolite composition. The samples are light-REE enriched with chondrite-normalised Ce (Ce_N) of 17–98, Yb_N of 4–14 and Ce_N/Yb_N of 2.6–15. While some samples have no Eu anomalies, others do have anomalies with inferred Eu/Eu^* values of down to ca. 0.4. Eleven samples have present-day⁸⁷Sr/⁸⁶Sr ratios between 0.7053 and 0.7100, and noting that some samples are up to 12 Ma old, initial⁸⁷Sr/⁸⁶Sr ratios are below ca. 0.709. These trace element and Sr isotope characteristics resemble those of contemporaneous andesite and dacite lavas, suggesting a common origin for all these rock types. The higher Rb/Sr ratios and larger Eu anomalies in most of the dacitic and rhyolitic ignimbrites are consistent with an origin by plagioclase-dominated fractional crystallization of mantle-derived andesite magma.     

Compositional characteristics and geodynamic significance of late Miocene volcanic rocks associated with the Chah Zard epithermal gold–silver deposit,southwest Yazd,Iran

Whole‐rock geochemical and Sr–Nd isotopic data are presented for late Miocene volcanic rocks associated with the Chah Zard epithermal Au–Ag deposit in the Urumieh‐Dokhtar Magmatic Arc (UDMA), Iran, to investigate the magma source, petrogenesis and the geodynamic evolution of the study area. The Chah Zard andesitic to rhyolitic volcanic rocks are characterized by significant Large Ion Lithophile Element (LILE) and Light Rare Earth Element (LREE) enrichment coupled with High Field Strength Element (HFSE) depletion. Our geochemical data indicate an adakitic‐like signature for the volcanic rocks (e.g. SiO₂ > 62 wt%, Al₂O₃ > 15 wt%, MgO < 1.5 wt%, Sr/Y > 70, La/Yb > 35, Yb < 1 ppm, and Y < 18 ppm, and no significant Eu anomalies), distinguishing them from the other volcanic rocks of the UDMA. The Chah Zard volcanic rocks have similar Sr and Nd isotopic compositions; the ⁸⁷Sr/⁸⁶Sr(i) ratios range from 0.704 902 to 0.705 093 and the ε_Nd(i) values are from +2.33 to +2.70. However, the rhyolite porphyry represents the final stage of magmatism in the area and has a relatively high ⁸⁷Sr/⁸⁶Sr ratio (0.705 811). Our data suggest that the andesitic magmas are from a heterogeneous source and likely to result from partial melting of a metasomatized mantle wedge associated with a mixture of subducted oceanic crust and sediment. These melts subsequently underwent fractional crystallization along with minor amounts of crustal assimilation. Our study is consistent with the model that the volcanic host rocks to epithermal gold mineralization in the UDMA are genetically related to late Miocene Neo‐Tethyan slab break‐off beneath Central Iran.     

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.     

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.     

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     

Genetic significance of chemical,isotopic, and petrographic features of some peralkaline salic rocks from the island of Pantelleria

An anorthoclase phenocryst separate from a pantellerite welded tuff and a slightly peralkaline nonhydrated sodatrachyte glass both have⁸⁷Sr/⁸⁶Sr ratios of0.7030 ± 0.0002. The sodatrachyte glass, withSiO₂ = 63,Al₂O₃ = 15.5,and CaO= 1.4wt%and Sr= 53ppm, is interpreted as an intermediate member in the differentiation sequence through which pantellerite melts were derived from primary mafic magmas. The very low⁸⁷Sr/⁸⁶Sr ratios, in conjunction with K/Rb ratios of 500 to 700 found for the sodatrachytes, show that the primary mafic magmas were derived from mantle material which had been depleted in incompatible elements by a much earlier episode of magma generation.     

Petrology of volcanic products younger than 42 ka on the Lipari–Vulcano complex (Aeolian Islands, Italy): an example of volcanism controlled by tectonics

Over the last 42 ka, volcanic activity at Lipari Island (Aeolian Arc, Italy) produced lava domes, flows and pyroclastic deposits with rhyolitic composition, showing in many cases evidence of magma mixing such as latitic enclaves and banding. In this same period, on nearby Vulcano Island, similar rhyolitic lava domes, pyroclastic products and lava flows, ranging in composition from shoshonite to rhyolite, were erupted. As a whole, the post-42 ka products of Lipari and Vulcano show geochemical variations with time, which are well correlated between the two islands and may correspond to a modification of the primary magmas. The rhyolitic products are similar to each other in their major elements composition, but differ in their trace element abundances (e.g. La ranging from 40 to 78 ppm for SiO₂ close to 75 wt%). Their isotopic composition is variable, too. The ⁸⁷Sr/⁸⁶Sr (0.704723–0.705992) and ¹⁴³Nd/¹⁴⁴Nd (0.512575–0.512526) ranges partially overlap those of the more mafic products (latites), having ⁸⁷Sr/⁸⁶Sr from 0.7044 to 0.7047 and ¹⁴³Nd/¹⁴⁴Nd from 0.512672 to 0.512615. ²⁰⁶Pb/²⁰⁴Pb is 19.390–19.450 in latites and 19.350–19.380 in rhyolites. Crystal fractionation and crustal assimilation processes of andesitic to latitic melts, showing an increasing content in incompatible elements in time, may explain the genesis of the different rhyolitic magmas. The rocks of the local crustal basement assimilated may correspond to lithotypes present in the Calabrian Arc. Mixing and mingling processes between latitic and rhyolitic magmas that are not genetically related occur during most of the eruptions. The alignment of vents related to the volcanic activity of the last 40 ka corresponds to the NNW–SSE Tindari–Letojanni strike-slip fault and to the correlated N–S extensional fault system. The mafic magmas erupted along these different directions display evidence of an evolution at different P_H2O conditions. This suggests that the Tindari–Letojanni fault played a relevant role in the ascent, storage and diversification of magmas during the recent volcanic activity.     

Geochemistry of Cenezoic volcanic rocks, Baja California, Mexico: Implications for the petrogenesis of post-subduction magmas

Late Cenozoic volcanism in Baja California records the effects of cessation of subduction at a previously convergent, plate margin. Prior to 12.5 m.y., when subduction along the margin of Baja ceased, the predominant volcanic activity had a calc-alkaline signature, ranging in composition from basalt to rhyolite. Acidic pyroclastic activity was common, and possibly represented the westermost, distal edge of the Sierra Madre Occidental province. After 12.5 m.y., however, the style and composition of the magmatic products changed dramatically. The dominant rock type within the Jaraguay and San Borja volcanic fields is a magnesian andesite, with up to 8% MgO at 57% SiO₂, low Fe/Mg ratios, and high Na/K ratios. These rocks have unusual trace-element characteristics, with high abundances of Sr (up to 3000 ppm), low contents of Rb; K/Rb ratios are very high (usually over 1000, and up to 2500), and Rb/Sr ratios are low (less than 0.01). Furthermore, La_n/Yb_n ratios are high, consistent with derivation from a mantle source with fractionated REE patterns. ⁸⁷Sr/⁸⁶Sr ratios are less than 0.7048, and usually less than 0.7040, whereas the pre-12.5 m.y. lavas have ⁸⁷Sr/⁸⁶Sr ratios between 0.7038 and 0.7063. We have previously termed these rocks bajaites, in order to distinguish them from other magnesian andesites. Bajaites also occur in southernmost Chile and the Aleutian Islands, areas which also have histories of attempted or successful ridge subduction.It is proposed that the bajaite series is produced during the unusual physico-chemical conditions operating during the subduction of young oceanic lithosphere, or subduction of a spreading centre. During normal subduction, the oceanic crust dehydrates, releasing volatiles (water, Rb and other large-ion lithophile elements) into the overlying wedge. Subduction of younger crust will result in a progressive decrease, and eventual cessation of the transfer of volatiles when subduction stops. Thermal rebound of the mantle may cause the slab to melt, perhaps under eclogitestable conditions. The resulting melt will be heavy-REE-depleted, perhaps dacitic, but will otherwise inherit MORB-like Rb/Sr and K/Rb ratios. The ascending melt will react with the mantle to form the source of the bajaitic rocks. Furthermore, any amphibole in the mantle, stabilised during the higher PH₂O conditions of earlier subduction, will break down and contribute a high-K/Rb ratio component.The implications of this study are that firstly, the subducted slab does not contribute a highly fractionated REE component in most modern arcs (i.e. the slab does not melt); secondly, Rb has a very short residence time in the mantle, and its abundance in arc rocks is a direct reflection of the input from the dehydrating slab; and thirdly, bajaitelike rocks may provide recognition of attempted or successful ridge subduction in the geologic past.     

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.     

Strontium isotope evidence for crustal contamination of calc-alkaline volcanic rocks from Cerro Galan,northwest Argentina

The Pampean Ranges of northwest Argentina are a basin-and-range tectonic province with a late Precambrian to Paleozoic basement and extensive Miocene-Recent calc-alkaline volcanism. The volcanoes include the large resurgent Cerro Galan caldera, and Recent scoria cones and lava flows. Miocene-Recent volcanic rocks of basalt to dacite composition from the Cerro Galan area exhibit a range of Rb/Sr ratios of 0.043–1.092 and initial⁸⁷Sr/⁸⁶Sr ratios of 0.7057–0.7115 with a clear positive correlation between⁸⁷Sr/⁸⁶Sr and⁸⁷Rb/⁸⁶Sr, indicating an apparent age of ca. 130 Ma. This relationship is interpreted to indicate that the Sr isotope variation in the Cerro Galan volcanic rocks results from mixing of a mantle-derived component with low⁸⁷Sr/⁸⁶Sr (<0.7057) and high Sr (>700 ppm) with a crustal component characterized by higher⁸⁷Sr/⁸⁶Sr (>0.7115) and lower Sr (<240 ppm). It is concluded that the mixing is best explained as a result of a small degree of selective crustal Sr contamination (ca. 10%) of a range of subsequently erupted magmas produced largely by fractional crystallization within the continental crust. We propose that the mantle-derived end-member is derived by partial melting of sub-Andean mantle with an⁸⁷Sr/⁸⁶Sr ratio of ca. 0.704, and that such an Sr isotope ratio characterizes the source region for calc-alkaline volcanic rocks throughout the Andes.     

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.     

Origin and evolution of mid-Cretaceous, garnet-bearing, intermediate and silicic volcanics from Canterbury, New Zealand

The Mt Somers Volcanics are part of a suite of mid-Cretaceous (89 ± 2 Ma) intermediate to silicic volcanics, erupted onto an eroded surface of Torlesse sediments. Rock types vary from basaltic andesite to high-silica rhyolite. Andesites are medium- to high-K with phenocrysts of plagioclase, orthopyroxene and pigeonite. Dacites are peraluminous and commonly contain granulite facies xenoliths and garnet xenocrysts. Equilibrium mineral assemblages indicate metamorphic pressures of close to 6 kbar at 800°C. Rhyolites are peraluminous with phenocrysts of quartz, sanidine, plagioclase, biotite, garnet and orthopyroxene. The ferromagnesian phases show textural evidence of magmatic crystallization and are chemically distinct from xenocryst phases in dacites. Equilibrium assemblages indicate that early magmatic crystallization occurred at close to 7 kbar (20 km depth) at above 850°C, with melt-water contents of less than 3.5%. Major-element contents, trace-element contents and an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.7085 indicate that the rhyolites formed by partial melting of dominantly quartzo-feldspathic Torlesse sediments, leaving a granulite-facies residue. The chemical variation displayed by the rhyolites is best explained by fractional crystallization of the observed high-pressure phenocryst assemblage. Most elements show a compositional gap between rhyolite and dacite. The major-element, trace-element and Sr isotope compositions of the intermediate lavas are best explained by assimilation of lower crustal material combined with fractional crystallization in mantle-derived tholeiitic magmas. Magmatism was the result of heat and magma flux from the mantle, during the change from compressive to extensional tectonics after the culmination of the Rangitata Orogeny.     

143Nd/144Nd,87Sr/86Sr and trace element constraints on the petrogenesis of Aleutian island arc magmas

¹⁴³Nd/¹⁴⁴Nd,⁸⁷Sr/⁸⁶Sr and trace element results are reported for volcanic and plutonic rocks of the Aleutian island arc. The Nd and Sr isotopic compositions plot within the mantle array with ε_Nd values of from 6.5 to 9.1 and⁸⁷Sr/⁸⁶Sr ratios of from 0.70289 to 0.70342. Basalts have mildly enriched light REE abundances but essentially unfractionated heavy REE abundances, while andesites exhibit a greater degree of light to heavy REE fractionation. Both the basalts and andesites have significant large ion lithophile element to light rare earth element (LILE/LREE) enrichments. Variations in the isotopic compositions of Nd and Sr are not related to the spatial distribution of volcanoes in the arc, nor are they related to temporal differences. ε_Nd and⁸⁷Sr/⁸⁶Sr do not correlate with major element compositions but do, however, correlate with certain LILE/LREE ratios (e.g. Ba_N/La_N). Plutonic rocks have isotropic and trace element characteristics identical to some of the volcanic rocks. Rocks that make up the tholeiitic, calc-alkaline and alkaline series in the Aleutians do not come from isotopically distinct sources, but do exhibit some differing LILE characteristics.Given these elemental and isotopic constraints it is shown that the Aleutian arc magmas could not have been derived directly from homogeneous MORB-type mantle, or fresh or altered MORB subducted beneath the arc. Mixtures of partially altered MORB with deep-sea sediment can in principle account for the isotopic characteristics and most of the observed LILE/LREE enrichments. However, some samples have exceedingly high LILE/LREE enrichments which cannot be accounted for by sediment contamination alone. For these samples a more complex scenario is considered whereby dehydration and partial melting of the subducted slab, containing less than 8% sediment, produces a LILE-enriched (relative to REE) metasomatic fluid which interacts with the overlying depleted mantle wedge. The isotopic and LILE characteristics of the mantle are extremely sensitive to metasomatism by small percentages of added fluid, whereas major elements are not substantially effected, Major element compositions of Aleutian magmas are dominantly controlled by the partial melting of this mantle and subsequent crystal fractionation; whereas isotopic and LILE characteristics are determined by localized mantle heterogeneities.     

Geochemistry of quaternary volcanism in the Sunda-Banda arc, Indonesia, and three-component genesis of island-arc basaltic magmas

Volcanic rocks of the Sunda and Banda arcs range from tholeiitic through calcalkaline and shoshonitic to leucititic, the widest compositional span of mafic magmatism known from an active arc setting.Mafic rocks in our data set, which includes 315 new analyses of volcanic rocks from twelve Quaternary volcanoes, including Batu Tara in the previously geochemically unknown Flores-Lembata arc sector, are generally similar to those from other island arcs: most contain <1.3 wt. % TiO₂ and 16–22 wt. % Al₂O₃, and have characteristically high K/Nb and La/Nb values. Abundances of P, Ba, Rb, Sr, La, Ce, Nd, Zr and Nb increase sympathetically with increasing K₂O contents of mafic rocks but those of Na, Ti, Y and Sc vary little throughout the geochemical continuum from low-K tholeiitic to high-K leucititic rocks.Excluding Sumatra and Wetar, which possess mainly dacitic and rhyolitic volcanics, the Sunda-Banda arc is divisible into four geochemical arc sectors with boundaries that correlate with major changes in regional tectonic setting and geological history. From west to east, the West Java, Bali and Flores arc sectors each comprise volcanoes which become progressively more K-rich eastwards, culminating in the leucitite volcanoes Muriah, Soromundi and Sangenges, and Batu Tara, respectively. In the most easterly Banda sector, the volcanics vary from high- to low-K eastwards around the arc.Correlations between geochemistry and ⁸⁷Sr/⁸⁶Sr values show separate trends for each of the four arc sectors, believed to be the result of involvement of at least three geochemically and isotopically distinct components in the source regions of the arc magmatism.A dominant source component with a low K content and a low ⁸⁷Sr/⁸⁶Sr value, and common to all sectors, is probably peridotitic mantle. A second component, with low K content but high ⁸⁷Sr/⁸⁶Sr value, appears to be crustal material. This component is most apparent in the Banda sector, in keeping with that sector's tectonic setting close to Precambrian Australian continental crust, but it is also present to lesser extents in the West Java and Flores sectors.However, the most marked geochemical and isotopic variations shown by the arc volcanics are primarily due to the involvement of a third component, which is rich in K-group elements but has relatively low ⁸⁷Sr/⁸⁶Sr values. This component appears to be mantle-derived and is least overprinted by crustal material in the Bali sector volcanics where the Pb, Be, U-Th and O isotope characteristics of the rocks support the suggestion that their genesis has not involved incorporation of recently subducted, continent-derived sialic material.The high, regionally persistent, Th/U value (about 4.3) of the Sunda subarc mantle, obtained from U-Th isotopic data, suggests a close association could exist between the K-rich component and the southern hemisphere ‘DUPAL’ mantle isotopic anomaly.     

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.     

Potassium-rich volcanic rocks of the Muriah complex, Java, Indonesia: Products of multiple magma sources?

The extinct Pleistocene volcano Muriah, situated behind the main Pleistocene—Recent Sunda magmatic arc in north-central Java, has erupted at least two contrasted groups of lavas. One group forms a well-defined compositional series (Anhydrous Series) from leucite basanite to tephritic phonolite, with olivine and tschermakitic clinopyroxene the main phenocrysts. The other group, the “Hydrous Series”, includes compositionally variable tephrites and high-K andesites with common plagioclase, biotite and amphibole. Lavas of the Anhydrous Series are much richer in LIL trace elements than the most potassic lavas of neighbouring active volcanoes, but relative HFS element enrichment is less pronounced. REE patterns have almost constant slopes from La (250–600 times chondrites) to Yb (5–10 times chondrites), while those of lavas of active centres are less light-enriched, and show flattening in the heavy REE. Anhydrous Series initial ⁸⁷Sr/⁸⁶Sr ratios (0.7043–0.7046) are lower than those of active centres (0.7047–0.7053). Hydrous Series lavas are intermediate in all these geochemical characteristics.The most mafic A-series leucite basanite, with Mg/(Mg + Fe²⁺) 0.69, 140 ppm Ni and 620 ppm Cr was probably derived from the primary magma for the series by fractionation of only 5 wt.% olivine. Its REE pattern suggests derivation from a garnet-bearing source. Experiments on this basanite, with up to 10% olivine and 20% orthopyroxene added, and in the presence of H₂O and H₂O/CO₂ mixtures, have shown that for all but very high magma water contents, the olivine and garnet liquidus fields are widely separated by fields of phlogopite and clinopyroxene. There is no liquidus field of orthopyroxene. Hence, if magma production involved an equilibrium melting process alone, the most probable sources are of garnet-bearing phlogopite clinopyroxenite type. Alternatively, this magma may represent the end-product of interaction between a low-K basanite magma from a garnet lherzolite source in the asthenosphere and a phlogopite-bearing lherzolite zone in the lower lithosphere. Its production was probably related to crustal doming and extension superimposed on the dominant subduction regime. Hydrous Series magmas may have resulted from mixing between Anhydrous Series magmas and high-K calc-alkaline basaltic to andesitic magmas more directly related to subduction processes.     

Strontium isotope ratios in volcanic rocks from the South Sandwich Islands

⁸⁷Sr/⁸⁶Sr ratios in the island-arc tholeiite series from the South Sandwich Islands cluster about a value of 0.7040. There is no apparent correlation of strontium isotope values with any major chemical component or with Rb/Sr ratios. The uniformity of the⁸⁷Sr/⁸⁶Sr values is consistent with the fractional crystallization relationship previously proposed for this suite. Though higher than values reported for ocean-floor tholeiites they are not significantly different from ratios reported for calc-alkaline island-arcs.     

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.     

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.