Origin of some calc-alkalic andesites in the Japanese Islands

Origin of calc-alkalic andesite in the Japanese Islands is reviewed on the basis of the recent trace element data and new experimental results. It is suggested that calc-alkalic andesites in the Japanese Islands have at least four different origins; (1) fractional crystallization with separation of magnetite of high-alumina basalt magma, (2) partial melting of hydrous upper mantle peridotite (for magnesian andesite), (3) fractional crystallization with separation of olivine and/or orthopyroxene of magnesian andesite magma and (4) mixing of dacitic and basaltic magmas. Emphasis is placed on the possible generation of primary magnesian calc-alkalic andesite magmas by direct partial melting of the upper mantle peridotite under hydrous conditions at depths between 40 and 60 km.     

Oxygen and strontium isotopic characteristics of calc-alkalic volcanic rocks from the central and western Japan arcs: Evaluation of contribution of crustal components to the magmas

¹⁸O/¹⁶O and ⁸⁷Sr/⁸⁶Sr ratios were determined for Quaternary calc-alkalic volcanic rocks from six volcanic rock suites in the central and western Japan arcs. The δ¹⁸O values relative to SMOW and ⁸⁷Sr/⁸⁶Sr ratios range from +6.3 to +9.9⁰/₀₀ and 0.70357 to 0.70684, respectively. Both the O- and Sr-isotopic compositions are higher than those for island-arc primitive magmas and their differentiates. The isotopic compositions of the calc-alkalic rocks cannot be derived by a simple fractional crystallization of the primitive magmas. On the other hand, the ¹⁸O- and ⁸⁷Sr-enrichment is confined to the rock suites located in well-developed island arcs having thick continental-type crust with low or negative Bouguer anomalies. Involvement of ¹⁸O- and ⁸⁷Sr-rich crustal material in the magma formation is suggested.The isotopic compositions vary remarkably within individual rock suites as well as from volcano to volcano. The data points in δ¹⁸O vs. ⁸⁷Sr/⁸⁶Sr plot accord with a mixing model between primitive magmas and crustal material of dioritic composition on an average, assuming their comparative Sr contents. The primitive magmas involved could not be low-Sr tholeiites, but magmas more or less enriched in incompatible elements including Sr, which correspond to high-alkali tholeiites or alkali basalts and their evolved magmas. The nature of the primitive magmas seems to change from tholeiitic to more alkalic with progressing island-arc evolution.Mixing of crust-derived melts is more plausible than assimilation of solid-rocks for involving 20 to 30% crustal material in the magmas along simple mixing curves. Isotopic variations between the rock suites are ascribed to variable Sr concentration radio of the end-members, variable isotopic compositions of crustal material or variable mixing ratio of the end-members. Extremely high-δ ¹⁸O rocks with moderate increase in ⁸⁷Sr/⁸⁶Sr ratio suggest another mixing process in shallower magma chambers between andesite magmas and metasedimentary rocks having high δ ¹⁸O and ⁸⁷Sr/⁸⁶Sr values but low Sr content. Subsequent fractional crystallization of once-derived magmas would be the prominent process for the rock suites showing gradual increase in ¹⁸O up to 1⁰/₀₀ with uniform ⁸⁷Sr/⁸⁶Sr ratios.     

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

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

The influence of crustal structure on compositions of subduction-related magmas

A survey of Sr isotopic ratios and other compositional features of subduction-related magma suites reveals significant correlations between these averaged parameters and characteristics of the underlying crust (i.e., thickness, composition, and age). These observations lead to the conclusion that crust and(or) mantle rocks in the hanging walls of subduction zones are involved in modification of primary mafic magmas (typically basalt or basaltic andesite). It is proposed that mafic magmas will stagnate within the crust or uppermost mantle where they may differentiate and react with wall rocks. The extent to which such processes manifest themselves will depend upon details of the local crustal structure. In particular, the composition and age of the crust will strongly influence such parameters as Sr, Nd and Pb isotopic compositions. Such data strongly indicate the involvement of crustal rocks in locales underlain by old sialic crust (e.g., central Andes). Depending upon the level of magma stagnation and evolution within the crust, different trends in isotopic composition may result. These isotopic trends may be enhanced by partial melting of the wall rocks to produce relatively silicic anatectic magmas, and locally they may reflect subduction of continental sediments. Interpretation of the isotopic data may be more ambiguous in locales underlain by younger and more mafic continental crust (Cascades, E Eleutians) and those underlain by oceanic crust owing to the similarity in isotopic composition of primary magmas and the latter crustal materials. Yet some degree of crustal involvement in magmatic evolution seems highly probable even in these more primitive terranes. Consequently, most island arc magmas, and especially those more evolved than basalt, are probably not primary in the sense that they do not represent direct melts of the upper mantle. Studies of arc volcanic rocks may yield misleading conclusions concerning processes of magma generation related to subduction unless evolutionary processes are defined and their effects considered. It appears that modern volcanic arcs provide a poor analog for models of early crustal development because the modern mantle-derived magmatic components are more mafic in composition than average continental crust.     

Adakitic magmas in the Ecuadorian Volcanic Front: Petrogenesis of the Iliniza Volcanic Complex (Ecuador)

The Iliniza Volcanic Complex (IVC) is a poorly known volcanic complex located 60 km SSW of Quito in the Western Cordillera of Ecuador. It comprises twin peaks, North Iliniza and South Iliniza, and two satellite domes, Pilongo and Tishigcuchi. The study of the IVC was undertaken in order to better constrain the role of adakitic magmas in the Ecuadorian arc evolution. The presence of volcanic rocks with an adakitic imprint or even pristine adakites in the Ecuadorian volcanic arc is known since the late 1990s. Adakitic magmas are produced by the partial melting of a basaltic source leaving a garnet rich residue. This process can be related to the melting of an overthickened crust or a subducting oceanic crust. For the last case a special geodynamic context is required, like the subduction of a young lithosphere or when the subduction angle is not very steep; both cases are possible in Ecuador. The products of the IVC, made up of medium-K basaltic andesites, andesites and dacites, have been divided in different geochemical series whose origin requires various interactions between the different magma sources involved in this subduction zone. North Iliniza is a classic calc-alkaline series that we interpret as resulting from the partial melting of the mantle wedge. For South Iliniza, a simple evolution with fractional crystallization of amphibole, plagioclase, clinopyroxene, magnetite, apatite and zircon from a parental magma, being itself the product of the mixing of 36% adakitic and 64% calc-alkaline magma, has been quantified. For the Santa Rosa rhyolites, a slab melting origin with little mantle interactions during the ascent of magmas has been established. The Pilongo series magma is the product of a moderate to high degree (26%) of partial melting of the subducting oceanic crust, which reached the surface without interaction with the mantle wedge. The Tishigcuchi series shows two stages of evolution: (1) metasomatism of the mantle wedge peridotite by slab melts, and (2) partial melting (10%) of this metasomatized source. Therefore, the relative ages of the edifices show a geochemical evolution from calc-alkaline to adakitic magmas, as is observed for several volcanoes of the Ecuadorian arc.     

Petrological variation of large-volume felsic magmas from Hakkoda-Towada caldera cluster: Implications for the origin of high-K felsic magmas in the Northeast Japan Arc

Abstract The Hakkoda‐Towada caldera cluster (HTCC) is a typical Late Cenozoic caldera cluster located in the northern part of the Northeast Japan Arc. The HTCC consists of five caldera volcanoes, active between 3.5 Ma and present time. The felsic magmas can be classified into high‐K (HK‐) type and medium‐ to low‐K (MLK‐) type based on their whole‐rock chemistry. The HK‐type magmas are characterized by higher K₂O and Rb contents and higher ⁸⁷Sr/⁸⁶Sr ratios than MLK‐type magmas. Both magmas cannot be derived from fractional crystallization of any basaltic magma in the HTCC. Assimilation‐fractional crystallization model calculations show that crustal assimilation is necessary for producing the felsic magmas, and HK‐type magmas are produced by higher degree of crustal assimilation with fractional crystallization than MLK‐type magmas. Although MLK‐type magmas were erupted throughout HTCC activity, HK‐type magmas were erupted only during the initial stage. The temporal variations of magma types suggest the large contribution of crustal components in the initial stage. A major volcanic hiatus of 3 my before the HTCC activity suggests a relatively cold crust in the initial stage. The cold crust probably promoted crustal assimilation and fractional crystallization, and caused the initial generation of HK‐type magmas. Subsequently, the repeated supply of mantle‐derived magmas raised temperature in the crust and formed relatively stable magma pathways. Such a later system produced MLK‐type magmas with lesser crustal components. The MLK‐type magmas are common and HK‐type magmas are exceptional during the Pliocene–Quaternary volcanism in the Northeast Japan Arc. This fact suggests that exceptional conditions are necessary for the production of HK‐type magmas. A relatively cold crust caused by a long volcanic hiatus (several million years) is considered as one of the probable conditions. Intensive crustal assimilation and fractional crystallization promoted by the cold crust may be necessary for the generation of highly evolved HK‐type felsic magmas.     

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.     

The Zealandia Volcanic Complex: Further evidence of a lower crustal “hot zone” beneath the Mariana Intra‐oceanic Arc,Western Pacific

This paper addresses formation of felsic magmas in an intra‐oceanic magmatic arc. New bathymetric, petrologic, geochemical, and isotopic data for Zealandia Bank and two related volcanoes in the south‐central Mariana arc is presented and interpreted. These three volcanoes are remnants of an older andesitic volcano that evolved for some time and became dormant long enough for a carbonate platform to grow on its summit before reawakening as a rhyodacitic volcano. Zealandia lavas are transitional between low‐ and medium‐K and tholeiitic and calc‐alkaline suites. They define a bimodal suite with a gap of 56–58 wt% SiO₂; this suggests that mafic and felsic magmas have different origins. The magmatic system is powered by mantle‐derived basalts having low Zr/Y and flat rare earth element patterns. Two‐pyroxene thermometry yields equilibration temperatures of 1000–1100 °C for andesites and 900–1000 °C for dacites. Porphyritic basalts and andesites show textures expected for fractionating magmas but mostly fine‐grained felsic lavas do not. All lavas show trace element signatures expected for mantle and crustal sources that were strongly melt‐depleted and enriched by subduction‐related fluids and sediment melts. Sr and Nd isotopic compositions fall in the normal range of Mariana arc lavas. Felsic lavas show petrographic evidence of mixing with mafic magma. Zealandia Bank felsic magmatism supports the idea that a large mid‐ to lower‐crustal felsic magma body exists beneath the south‐central Mariana arc, indicating that MASH (mixing, assimilation, storage, and homogenization) zones can form beneath intra‐oceanic as well as continental arcs.     

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.     

A Jurassic-Cretaceous island arc in the Ladakh-Himalayas

The Ladakh Mesozoic ophiolite belt (western Himalaya) contains a pile of volcanic thrust sheets (Dras unit) which differ significantly in structure and composition from the ophiolitic mélange zones. The Dras unit is composed of pillow lavas, doleritic sills, very irregular basaltic (?basaltic andesites) and dacitic flows intercalated with pyroclastics, volcanoclastic sediments and radiolarian cherts. According to fossil evidence, this volcanism must have been active between Upper Jurassic and Upper Cretaceous.The presence of relict primary minerals, such as magnesiochromite, clinopyroxene, hastingsitic hornblende and Ti-magnetite as well as distinctive bulk chemistries, suggests that the volcanics belong to island arc tholeiite and to calc-alkaline rock series, typical of present island arcs in the Caribbean and Pacific.Model calculations incorporating probed phenocryst phases indicate that in addition to olivine, clinopyroxene and plagioclase, amphibole and titanomagnetite are crucial fractionating phases in the development of the dacites from a primitive tholeiitic melt. The latter process must have taken place at about 1000°C and at moderate depth of 5–15 km within or underneath the island arc. Today, hornblende-bearing mafic cumulates appear in the vicinity of Kargil within and close to the Dras volcanics.In a Sr-evolution diagram, the Dras volcanics have yielded a “pseudo-isochron” with a low initial ratio of 0.7035 ± 0.0003, which is in the same range as the mean of modern island arc volcanics. However, a geologically unrealistic age of 263 m.y., is obtained from the slope of this isochron.The upper mantle is regarded as the source material for the island arc tholeiitic magmas. Enrichment in K, Ba, Sr and LREE supports the involvement of components derived from dehydration or incipient melting of subducted Tethyan oceanic crust in the mantle.     

Evidence for magma mixing in the Mariana arc system

Volcanoes of the Mariana arc system produce magmas that belong to several liquid lines of descent and that originated from several different primary magmas. Despite differences in parental magmas, phenocryst assemblages are very similar throughout the arc. The different liquid lines of descent are attributed to differences in degree of silica saturation of the primary liquids and in the processes of magmatic evolution (fractional crystallization vs magma mixing). Pseudoternary projections of volcanic rocks from several arc volcanoes are used to show differences between different magmatic suites. In most of the arc, parental liquids were Ol- and Hy-normative basalts that crystallized olivine, augite, and plagioclase (± iron-titanium oxide) and then plagioclase and two pyroxenes, apparently at low pressure. Eruptive rocks follow subparallel liquid lines of descent on element–element diagrams and on pseudoternary projections. Magmas at North Hiyoshi are Ne-normative and have a liquid line of descent along the thermal divide due to precipitation of olivine, augite, and plagioclase. Derived liquids are large ion lithophile element (LILE)-rich. Magmas at other Hiyoshi seamounts included an alkaline component but had more complex evolution. Those at Central Hiyoshi formed by a process dominated by mixing alkaline and subalkaline magmas, whereas those at other Hiyoshi seamounts evolved by combined magma mixing and fractional crystallization. Influence of the alkaline component wanes as one goes south from North Hiyoshi. Alkaline and subalkaline magmas were also mixed to produce magmas erupted at the Kasuga seamounts that are behind the arc front. The alkaline magmas at both Hiyoshi and Kasuga seamounts had different sources from those of the subalkaline magmas at those sites as indicated by trace element ratios and by _Nd.     

Compositions of deep-sea ash layers derived from north pacific volcanic arcs: variations in time and space

Glass separates from 115 ash layers derived from the Kamchatkan (DSDP Site 192; 34 layers), the eastern Aleutian (DSDP Site 183; 56 layers) and the Alaska Peninsula (DSDP Site 178; 25 layers) volcanic arcs have been analyzed for up to 28 elements. In addition, the abundance and diversity of associated mafic phenocrysts have been evaluated. The resulting data set has made possible an evaluation of the late Miocene to Recent changes in composition of ashes derived from North Pacific volcanic arcs and of the factors controlling the evolution of highly siliceous magmas.We find no evidence for a general transition from arc tholeiite to calc-alkalic magma parentage of ashes derived from the volcanic arcs during the last 10 m.y., but instead find 0.1- to 0.5-m.y. intervals during which particular types of volcanism are prevalent. Most convincing is the transition from arc tholeiite to calc-alkalic for ashes derived from Kamchatka during the last 0.8 m.y., a change believed to be associated with a landward shift in the site of magma generation. Considered together, ashes derived from North Pacific volcanic arcs have been becoming more siliceous during the last 1.5 m.y. and may be associated with accelerated subduction during the same time interval.Hydrous phenocrysts (e.g., biotite) are typically associated with low-silica deep-sea ashes, but not with terrestrial volcanic rocks of comparable silica contents, suggesting the important role of water in the evolution of siliceous magma. REE patterns and relative abundances of mafic phenocrysts demonstrate the importance of fractional crystallization in controlling the evolution of highly siliceous arc magmas. REE increase with increasing silica, but become less concentrated in ashes with SiO₂ > 64%. Eu anomalies increase throughout the SiO₂ range. Initial fractionation is dominated by clinopyroxene and plagioclase with amphibole strongly influencing fractionation above 64% SiO₂.     

Bimodal tholeiitic and mildly alkalic basalts from Bhir area,central Deccan Volcanic Province,India: Geochemistry and petrogenesis

Bimodal tholeiitic and mildly alkalic basalts occur near Bhir, in the central part of Deccan Volcanic Province (DVP). Major and trace element concentrations show that, of the ten flows, nine are tholeiitic and one is an alkalic basalt. The Bhir basalts have a wide range of chemical composition. Geochemical variations in the stratigraphic section define three distinct phases of evolution (zones 1 to 3). Crystal fractionation of plagioclase, clinopyroxene, olivine and Fe–Ti oxide expanded the compositional range. Low Mg#s (39–55), low concentrations of Ni and Cr and high Zr suggest the evolved nature of the Bhir basalts. Fractionation modeling suggests about 42% fractional crystallization.In spite of the dominant role of fractional crystallization in the evolution of Bhir basalts, some other processes must be sought to explain the chemical variations. Crustal contamination, magma mixing and degree of partial melting are suggested to explain the observed chemical variations. Resorption, reverse zoning and compositional bimodality in plagioclase phenocrysts indicate magma mixing. Samples of flows one and four suspected of being contaminated all have enriched SiO₂ and LILE (K, Rb, and Ba) contents and depletion in Ti and P, believed to be due to ‘granitic’ crustal contamination.As compared to tholeiitic basalts, the alkalic basalts are characterized by low SiO₂ and high TiO₂, Na₂O, K₂O and P₂O₅. Alkalic basalts are richer in LILE (Rb and Ba), HFSE (Nb, Zr, and Y) and REE than the tholeiitic basalts. The alkalic basalt occurrence is important from a petrogenetic point of view and also suggests that the sources of alkalic basalt magmas may be of variable ages under different parts of the DVP. Based on major, trace and rare earth element distributions it is suggested that asthenospheric mantle having affinities with the source of OIB was the source material of the magmas and the range in the composition of tholeiitic and alkalic basalts was probably controlled by different degrees of melting and/or inhomogeneities in the mantle source.     

Evolution of the tertiary volcanic rocks in the Izu-Mariana arc

Petrological evolution of the Tertiary island arc in the Izu-Mariana region has been accompanied by the development of three different volcanic suites: 1) oceanridge basalt now exposed as the metamorphic basement on Yap; 2) island-arc tholeiites of Eocene to early Oligocene age characterized by low contents of incompatible elements at all levels of silica enrichment; and 3) calc-alkalic rocks of late Oligocene to early Miocene age showing higher contents of silica and incompatible elements. All these three suites have primitive, undifferentiated basalts or andesites (boninites) characterized by high Mg/Fe, Cr, and Ni, suggesting that they have been derived from an upper mantle peridotite at relatively high temperatures. The earliest volcanism appears to have occurred at a spreading ridge. Later, as subduction proceeded, the island-arc tholeiite magma may have been produced by the introduction of a smaller amount of water into the locus of fusion from the subducted oceanic crust. An increasingly larger amount of water introduced into the same region could have led to the development of the more siliceous, calc-alkalic magma, as represented typically by the boninite.     

An evaluation of the global variations in the major element chemistry of arc basalts

Arc volcanoes occur at convergent margins with a wide range in subduction parameters, and variations in these parameters might be expected to lead to variations in the chemistry of magmas parental to arcs. Major element analyses from approximately 100 volcanic centers within 30 arcs, normalized to 6% MgO to minimize the effects of crystal fractionation, display wide variations. Na₂O and CaO at 6% MgO (Na_6.0 and Ca_6.0) correlate remarkably well with the thickness of the overlying crust. These systematics are consistent with two possible models. In the first model, the crust behaves as a chemical filter; where the crust is thick, magmas crystallize at higher pressure and interact more extensively with the arc crust. Modeling of high-pressure crystallization and assimilation, however, does not reproduce the associated variations in Na_6.0 and Ca_6.0 without calling upon complicated combinations of fractionating phases and assimilants. In the second model, crustal thickness determines the height of the mantle column available for melting beneath arc volcanoes. If melting begins beneath arcs at similar depths, then the column of mantle that undergoes decompression melting is much shorter beneath the thickest arc crust. The shorter mantle column for arcs built on thick crust will lead to smaller extents of melting in the mantle, and hence higher Na_6.0 and lower Ca_6.0 in the parental magmas. Modeling shows that variations in the extent of melting in the mantle can easily account for the associated variations in Ca_6.0 and Na_6.0. The abundances of the other major elements at 6% MgO do not correlate well with crustal thickness, or any other subduction parameter. Co-variation of some of these other major elements (e.g., Si_6.0 and Fe_6.0) within individual arcs suggests that they are strongly influenced by local crustal level processes that obscure partial melting systematics. Correction for the crustal processes improves the relationship between Na_6.0 and Ca_6.0 that is so readily explained by partial melting. The extents of melting in the mantle beneath arc volcanoes estimated from the ranges in Na_6.0 and Ca_6.0 are remarkably similar to those estimated beneath mid-ocean ridges. This observation provides further evidence that the mantle wedge, and not the slab, melts beneath arc volcanic fronts.     

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.     

The magma evolution of Tianchi volcano, Changbaishan

The Changbaishan Tianchi volcano is composed of the basaltic rocks at the shield-forming stage, the trachyte and pantellerite at the cone-forming stage and modern eruption. Studies on their REE, incompatible elements and Sr, Nd, Pb isotopes suggest that rocks at different stages have a common magma genesis and close evolution relationship with differentiation crystallization playing the key role. The co-eruption of basaltic trachyandesite magma and pantellerite magma indicates that there exist both crustal magma chamber and mantle magma reservoir beneath the Tianchi volcano. Project supported by the National Natural Science Foundation of China (Grant No. 49672109).     

Trace-element and isotopic constraints on the source of magmas in the active volcano and Mariana island arcs, Western Pacific

Analytical results of the relative and absolute abundance of LIL-incompatible trace elements (K, Rb, Cs, Sr, and Ba) and isotopic compositions ( , , and ) are summarized for fresh samples from active and dormant volcanoes of the Volcano and Mariana island arcs. The presence of thickened oceanic crust (T 15–20 km) beneath the arc indicates that while hybridization processes resulting in the modification of primitive magmas by anatectic mixing at shallow crustal levels cannot be neglected, the extent and effects of these processes on this arc's magmas are minimized. All components of the subducted plate disappear at the trench. This observation is used to reconstruct the composition of the crust in the Wadati-Benioff zone by estimating proportions of various lithologies in the crust of the subducted plate coupled with analyses from DSDP sites. Over 90% of the mass of the subducted crust consists of basaltic Layers II and III. Sediments and seamounts, containing the bulk of the incompatible elements, make up the rest. Bulk Western Pacific seafloor has , δ ¹⁸O +7.2, K/Rb 510, K/Ba 46, and K/Cs 13,500. Consideration of trace-element data and combined systematics limits the participation of sediments in magmagenesis to less than 1%, in accord with the earlier results of Pb-isotopic studies. Combined data indicate little, if any, involvement of altered basaltic seafloor in magmagenesis. Perhaps more important than mean isotopic and LIL-element ratios is the restricted range for lavas from along over 1000 km of this arc. Mixtures of mantle with either the subducted crust or derivative fluids should result in strong heterogeneities in the sources of individual volcanoes along the arc. Such heterogeneities would be due to: (1) gross variations of crustal materials supplied to the subduction zone; and (2) lesser efficiency of mixing processes accompanying induced convection between arc segments (parallel to the arc) as compared to that perpendicular to the arc. The absence of these heterogeneities indicates that either some process exists for the efficient mixing of mantle and subducted material parallel to the arc or that subducted materials play a negligible role in the generation of Mariana-Volcano arc melts.Consideration of plausible sources in the mantle indicates that (1) an unmodified MORB-like mantle cannot have generated the observed trace-element and isotopic composition of this arc's magmas, while (2) a mantle similar to that which has produced alkali-olivine basalts (AOB) of north Pacific “hot spot” chains is indistinguishable in many respects spects from the source of these arc lavas.     

Melting experiments on hydrous low-K tholeiite: Implications for the genesis of tonalitic crust in the Izu–Bonin – Mariana arc

A series of water-deficient partial melting experiments on a low-K tholeiite were carried out under lower crustal P–T–H₂O conditions (900–1200 °C, 0.7–1.5 GPa, 2 and 5 wt% H₂O added) using a piston-cylinder apparatus. With increasing temperature at 1.0 GPa, supersolidus mineral assemblages vary from amphibolitic to pyroxenitic. Garnet crystallizes in the higher pressure runs (> 1.2 GPa). Melt compositions show low-K calc-alkalic trends, and are classified as metaluminous or peraluminous tonalite. These features are similar to the felsic rocks in the Izu–Bonin – Mariana (IBM) arc, for example Tanzawa plutonic rocks. The anatectic origin of Tanzawa tonalites is consistent with geochemical modeling, which demonstrates that the rare earth element (REE) characteristics of Tanzawa plutonic rocks (which represent the middle crust of the IBM arc) can be generated by partial melting of amphibolite in the lower crust (∼ 50% melting at 1050 °C and below 1.2 GPa). Estimated densities of pyroxenitic restites (∼ 3.9 g/cm³) after extraction of andesitic melts are higher than that of mantle peridotite beneath the island arc (3.3 g/cm³). The high density of the restite could cause delamination of the IBM arc lower crust. Rhyolitic magmas in the IBM arc (e.g. Niijima) could be formed by low degrees of partial melting of the amphibolitic crust at a temperature just above the solidus (10% melting at or below 900 °C).     

High-pressure inclusions in tholeiitic basalt and the range of lherzolite-bearing magmas in the Tasmanian volcanic province

Spinel-lherzolite xenoliths have been found in olivine tholeiite near Andover in the Tasmanian Tertiary volcanic province. They show a high-pressure mineralogy of predominant olivine (Mg₉₀), with aluminous enstatite (Mg₉₀) and lesser aluminous diopside and chrome-bearing spinel, and resemble lherzolite xenoliths commonly found in undersaturated lavas. Such xenoliths are unusual in tholeiitic basalts and the occurrence directly attests to a mantle origin for at least some tholeiitic magmas.The lherzolites are accompanied by doleritic and pyroxenitic xenoliths and by olivine, orthopyroxene, clinopyroxene and plagioclase xenocrysts. If near-liquidus phases are represented amongst the xenocrysts, then the magnesian number of the host basalt and its xenocryst assemblage provisionally suggest a magma derived by more than 15–20% partial melting of mantle peridotite, before commencing xenocryst crystallisation at pressures between 8–13 kbar.With this new record, lherzolite-bearing lavas in Tasmania now cover an extremely wide compositional range, extending from highly undersaturated olivine melilitite to olivine tholeiite. They also include a considerable number of fractionated alkaline rocks that are only sparsely reported in the literature as lherzolite hosts. This latter group contains representatives of a previously suggested but unestablished alkaline fractionation series based on olivine nephelinite, viz. calcic olivine nephelinite → sodic olivine nephelinite → potassi-sodic olivine nephelinite → mafic nepheline benmoreite → mafic phonolite.Lherzolite and megacryst-bearing lavas are relatively more abundant in peripheral parts to the main basalt sequences in Tasmania. This suggests that they developed in fringing zones of less intense mantle melting which enhanced stagnation and fractionation of magmas within the mantle before eruption. Calculated crustal thicknesses under these areas suggest that the magmas were generated at pressures exceeding 6–11 kbar, with the Andover tholeiitic magma exceeding 9 kbar.