Major- and trace-element systematics and isotope geochemistry of Cenozoic mafic volcanic rocks from the Vogelsberg (central Germany): Constraints on the origin of continental alkaline and tholeiitic basalts and their mantle sources

The Cenozoic basaltic province of the Vogelsberg area (central Germany) is mainly composed of intercalated olivine to quartz tholeiites and near-primary nephelinites to basanites. The inferred mantle source for the alkaline and tholeiitic rocks is asthenospheric metasomatized garnet peridotite containing some amphibole as the main hydrous phase. Trace element modelling indicates 2 to 3% partial melting for the alkaline rocks and 5 to 7% partial melting for the olivine tholeiites. Incompatible trace element abundances and ratios as well as Nd and Sr radiogenic isotope compositions lie between plume compositions and enriched mantle compositions and are similar to those measured in Ocean Island Basalts (OIB) and the Central European Volcanic Province elsewhere. The mafic olivine tholeiites have similar Ba/Nb, Ba/La and Nd–Sr isotope ratios to the alkaline rocks indicating derivation of both magma types from chemically comparable mantle sources. However, Zr/Nb ratios are slightly higher in olivine tholeiites than in basanites reflecting some fractionation of Zr relative to Nb during partial melting. Quartz tholeiites have higher Ba/Nb, Zr/Nb, La/Nb, but lower Ce/Pb ratios and lower Nd isotope compositions than the alkaline rocks which can be explained by interaction of the basaltic melt with lower (granulite facies) crustal material or partial melts thereof during stagnation within the lower crust. It appears most likely that upwelling of hot, asthenospheric material results in the generation of primitive alkaline rocks at the base of the lithosphere at depths of 75–90 km. Lithospheric extension together with minor plume activity and probably lower lithosphere erosion induced melting of shallower heterogenous upper mantle generating a spectrum of olivine tholeiitic melts. These olivine tholeiitic rocks evolved via crystal fractionation and probably limited contamination to quartz tholeiites.     

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.     

图们江流域新生代火山岩Sr、Nd同位素初步研究

中国地震局地质研究所; 中国地震局地质研究所 北京     

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.     

Petrology of basalts from Loihi Seamount,Hawaii

Loihi Seamount is the southeasternmost active volcano of the Emperor-Hawaii linear volcanic chain. It comprises a spectrum of basalt compositional varieties including basanite, alkali basalt, transitional basalt and tholeiite. Samples from four dredge collections made on Scripps Institution of Oceanography Benthic Expedition in October 1982 are tholeiite. The samples include highly vesicular, olivine-rich basalt and dense glass-rich pillow fragments containing olivine and augite phenocrysts. Both quartz-normative and olivine-normative tholeiites are present. Minor and trace element data indicate relatively high abundances of low partition coefficient elements (e.g., Ti, K, P. Rb, Ba, Zr) and suggest that the samples were derived by relatively small to moderate extent of partial melting, of an undepleted mantle source. Olivine composition, MgO, Cr and Ni abundances, and Mg/(Mg+Fe), are typical of moderately fractionated to relatively unfractionated “primary” magmas. The variations in chemistry between samples cannot be adequately explained by low-pressure fractional crystallization but can be satisfied by minor variations in extent of melting if a homogeneous source is postulated. Alternatively, a heterogeneous source with variable abundances of certain trace elements, or mixing of liquids, may have been involved. Data for ³He/⁴He, presented in a separate paper, implies a mantle plume origin for the helium composition of the Loihi samples. There is little variation in the helium isotope ratio for samples having different compositions and textures. The helium data are not distinctive enough to unequivocally separate the magma sources for the tholeiitic rocks from the other rock types such as Loihi alkalic basalts and the whole source region for Loihi may have a nearly uniform helium compositions even though other element abundances may be variable. Complex petrologic processes including variable melting, fractional crystallization and magma mixing may have blurred original helium isotopic signatures.     

Origin of contemporaneous tholeiitic and K-rich alkalic lavas: a case study from the northern Deccan Plateau,India

Concurrently erupted, alternating Deccan Trap flows of tholeiitic and potassic alkalic basalt outcrop along both banks of the Narmada River near Navgam. Nearby, around Rajpipla, early tholeiites are overlain by K-rich alkalic flows and intrusives, which are themselves cut by later tholeiitic dikes. Nd and Sr isotopic ratios of a wide variety of rocks from both areas form a single correlated array, which reflects mixing between positive ε_JUV and negative ε_JUV endmembers. There is an almost complete overlap between values for tholeiitic and alkalic samples; thus, both alkalic and tholeiitic primary magmas must have been produced that were isotopically much alike. A Rajpipla rhyolite also falls on the array, near the midpoint. For positive values of ε_JUV(T) the array is indistinguishable from that defined by the lower group of tholeiites at Mahabaleshwar, some 450 km to the south, implying a similar or identical high ε_JUV mantle source. The negative ε_JUV component, apparently different from either of the two at Mahabaleshwar, may have been continental crust or enriched mantle. Both alkalic and tholeiitic groups display wide overlapping ranges in incompatible elements other than K, Rb, and Ba—particularly in Sr and Nb. This partial decoupling of incompatible elements, in conjunction with the isotopic similarity between the two classes of rocks, is strongly suggestive of an enrichment event in portions of the mantle source shortly before magmatism.     

Cenozoic volcanic and petrochemical provinces of Mainland Asia

Mainland Asia has been subdivided into 14 distinct volcanic petrochemical provinces. Alkaline rocks form about 88% of the extrusive materials. Potassic basalts form 62% of the basaltic “clan”. Andesitic rocks are relatively uncommon except near the seaboard and in Tibet. Peralkaline rocks are found in Korea and neighboring parts of China. The majority of the potassic basalt appear to be derived by variable degrees of partial melting of a mantle with lateral compositional heterogeneity. The peak of volcanic activity was during the Miocene and corresponded to the collision of the Indian continent and the development of back-arc basins.     

Major element, trace element, and Sr, Nd and Pb isotope studies of Cenozoic basalts from the South China Sea

The whole rock K-Ar ages of basalts from the South China Sea basin vary from 3.8 to 7.9 Ma, which suggest that intra-plate volcanism after the cessation of spreading of the South China Sea (SCS) is comparable to that in adjacent regions around the SCS, i.e., Leiqiong Peninsula, northern margin of the SCS, Indochina block, and so on. Based on detailed petrographic studies, we selected many fresh ba-saltic rocks and measured their major element, trace element, and Sr-Nd-Pb isotope compositions. Geochemical characteristics of major element and trace element show that these basaltic rocks belong to alkali basalt magma series, and are similar to OIB-type basalt. The extent of partial melting of mantle rock in source region is very low, and magma may experience crystallization differentiation and cu-mulation during the ascent to or storing in the high-level magma chamber. Sr-Nd-Pb isotopic data of these basaltic rocks imply an inhomogeneous mantle below the South China Sea. The nature of magma origin has a two end-member mixing model, one is EM2 (Enriched Mantle 2) which may be originated from mantle plume, the other is DMM (Depleted MORB Mantle). Pb isotopic characteristics show the Dupal anomaly in the South China Sea, and combined with newly found Dupal anomaly at Gakkel ridge in Arctic Ocean, this implies that Dupal anomaly is not only limited to South Hemisphere. In variation diagrams among Sr, Nd and Pb, the origin nature of mantle below the SCS is similar to those below Leiqiong peninsula, northern margin of the SCS and Indochina peninsula, and is different from those below north and northeast China. This study provides geochemical constraints on Hainan mantle plume.     

Petrogenesis of the Tanzawa plutonic complex, central Japan: Exposed felsic middle crust of the Izu–Bonin – Mariana arc

The Miocene Tanzawa plutonic complex, consisting mainly of tonalite intrusions, is exposed at the northern end of the Izu–Bonin – Mariana (IBM) arc system as a consequence of collision with the Honshu Arc. The Tanzawa plutonic rocks belong to the calc-alkaline series and exhibit a wide range of chemical variation, from 43 to 75 wt% SiO₂. They are characterized by relatively high Ba/Rb and Ce/Nb ratios, and low abundances of K₂O, LIL elements, and rare earth elements (REE). Their petrographic and geochemical features indicate derivation from an intermediate parental magma through crystal fractionation and accumulation processes, involving hornblende, plagioclase, and magnetite. The Tanzawa plutonic complex is interpreted to be the exposed middle crust of the IBM arc, which was uplifted during the collision. The mass balance calculations, combining data from melting experiments of hydrous basaltic compositions at lower-to-middle crustal levels, suggest that parental magma and ultramafic restite were generated by dehydration partial melting (∼ 45% melting) of amphibolite chemically similar to low-K tholeiitic basalt. Partial melting of hydrated mafic lower crust might play an important role in felsic middle-crust formation in the IBM arc.     

Petrology of arc volcanic rocks and their origin by mantle diapirs

Calc-alkalic chemical trends characteristic of arc volcanic rocks mainly result from three mechanisms which act additively: (1) fractional crystallization involving separation of titanomagnetite; (2) selective concentration of plagioclase phenocrysts and selective depletion of titanomagnetite phenocryst compared with the actually fractionated proportion; and (3) mixing of magmas on continuous fractionation trends. The association of calc-alkalic and tholeiitic trends in a single composite volcano may not represent different fractional crystallization processes or different chemistries of primary magmas, but the calc-alkalic chemical trend can be considered as a mixing trend resulting from mixing of various magmas on associated tholeiitic chemical trends. Chemical variations of most arc volcanic rocks, including calc-alkalic ones, can accordingly be essentially accounted for by the low-pressure fractional crystallization of phenocrystic phases from primary basaltic magmas.Crystallization sequences of arc magmas which are strongly dependent on water content in magmas are deduced from the phenocryst assemblages. The crystallization sequence changes laterally across-arc, suggesting increasing water contents in magmas toward the back-arc side, as is also seen for other incompatible elements such as K and Rb. Systematic differences in the characteristic crystallization sequence are also observed among arcs, roughly correlating with the crustal thickness. Water content in magma, like other incompatible elements, tends to increase with increasing crustal thickness. The variation of incompatible elements including water roughly represents that of the degree of partial melting of the upper mantle, which is broadly controlled by the crustal thickness.The variation of water content indicates that arc magmas are not saturated with water during differentiation to late differentiates such as dacite or rhyolite. This strongly constrains the maximum water contents in primary basaltic magma, at most 2.5 wt.%. This value suggests that magma generation beneath arcs is dependent on dry solidus of peridotite. Diapiric uprise of the hot deeper mantle and associated adiabatic decompression would be necessary for mantle peridotite to attain the temperature as high as dry solidus. Diapirs that begin to rise from the subduction zone may stop at or near the crust-mantle boundary because of the surrounding density change, and their degree of partial melting is roughly controlled by their stopped depth assuming their similar temperature. Across-arc variation is also explained by the stopped depth of diapirs, but is not controlled by crustal thickness.     

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.     

Petrogenetic relationships of acid and basic rocks in iceland: Sr-isotopes and rare-earth elements in late and postglacial volcanics

Strontium isotope ratios and rare-earth element abundances have been measured in acid, intermediate and basic rocks from three late to postglacial volcanic complexes, and several other postglacial basalts in Iceland. Late and postglacial basalts in Iceland have been generated from a source region which is essentially homogeneous with respect to⁸⁷Sr/⁸⁶Sr. The mean⁸⁷Sr/⁸⁶Sr ratio for the basalts analysed is 0.70328 and the range is from 0.70317 ± 6to0.70334 ± 5 (2σ).Acid rocks from the Kerlinganfjöll and Namafjall volcanic complexes have⁸⁷Sr/⁸⁶Sr ratios which are indistinguishable from analysed basalts from the same complexes. However, intermediate and acid rocks from the Torfajökull complex have significantly higher⁸⁷Sr/⁸⁶Sr ratios and could not have been derived by fractional crystallization from basaltic magmas similar to those found in the same complex. These latter rocks have most probably been produced by remelting of Tertiary gabbroic rocks in Layer 3. Most of the basalts analysed have higher total rare-earth element abundances than typical dredged ocean-ridge tholeiites, and show less light rare-earth depletion. Intermediate and acid compositions show overall higher abundances and light rare-earth enrichments. The measured rare-earth abundances are compared with abundances generated by differential partial melting of various model source regions.It is shown that both the tholeiitic and alkali basalt compositions could be generated from the same source material by different degrees of partial melting. Variable partial melting of gabbroic material may account for the rare-earth element abundances of both the rhyolitic rocks (small degrees of melting) and the intermediate rocks (more extensive melting).     

Geochemical and petrological relations in some deccan basalts, Western Maharashtra, India

Petrographic and geochemical data are given for some basaltic rocks from the Koynaghat, Ambaghat and Panvel sections of the western Deccan volcanic province. This study confirms geochemical features established earlier for the Deccan basalts but brings out minor additional characters. Mineralogical and major-element compositions of the basaltic flows from the Koyna and Panvel sections indicate tholeiitic affinity; the Ambaghat flows exhibit a slight affinity towards alkali basalt. Rare earth element (REE) distribution patterns and trace-element abundances suggest minor fractionation of olivine and plagioclase during the evolution of the flows. The general similarity of chemical and mineralogical features over a wide area and the lack of conspicuous inter-element relationships suggest that the flows reflect the combined effects of partial melting, minor mineral fractionation and selective crustal contamination.     

The geochemical characteristics and conditions of petrogenesis of the volcanic rocks of the northern lesser antilles — A review

This paper is concerned with the islands of Montserrat Nevis, St. Kitts, St. Eustatius and Saba, which lie on the inner volcanic are at the northern of the Lesser Antilles. Andesites greatly predominate over basalts and dacites in this part of the arc. Generally the lavas from the northern Lesser Antilles contain low abundances of Ni, Cr and residual trace elements but lavas from Saba are enriched in these elements compared with the other islands in the group. The most important petrogenetic process in this part of the Lesser Antilles is probably partial melting of subducted oceanie tholeiite and this process accounts satisfactorily for the chemistry (especially the low Ni, Cr) and large volumes of the erupted andesites. Some andesites have, however, been produced by fractional crystallisation of basaltic magma and magma mixing probably accounts for some of the peculiar chemical and petrographic properties of the Saba andesites. The rocks from the Northern Lesser Antilles are different from those in the central part of the arc (more acid rocks, higher residual trace elements) and the southern islands have much higher proportions of basalt, some of it undersaturated and alkaline. It is thought that partial melting of mantle peridotite may be the predominant petrogenetic process at the southern end of the Lesser Antilles whereas partial melting of subducted oceanic crust is more important in the north.     

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.     

Material records for Mesozoic destruction of the North China Craton by subduction of the Paleo-Pacific slab

It is well known that the destruction of the North China Carton(NCC) is closely related to subduction of the PaleoPacific slab, but materials recording such subduction has not been identified at the peak time of decratonization. This paper presents data of whole-rock major and trace elements and Sr-Nd-Hf isotopes and zircon U-Pb ages and Hf-O isotopes for Mesozoic volcanic rocks from the Liaodong-Jinan region in the northeastern NCC, in order to trace the subduction-related materials in their source and origin. The Mesozoic volcanic rocks in the Liaodong-Jinan region are mainly composed of two series of rocks, including alkaline basaltic trachyandesite, trachyandesite and trachyte, and subalkaline trachyandesite and andesite. Zircon U-Pb dating yields eruption ages of 129–124 Ma for these rocks. The Early Cretaceous volcanic rocks are all enriched in LILEs(such as Rb, Sr, Ba and Th) and LREEs, depleted in HFSEs(such as Nb, Ta and Ti), indicating that they were originated from mantle sources that had been modified by subducted crustal materials. However, they have relatively heterogeneous and variable isotopic compositions. The alkaline basaltic trachyandesite, trachyandesite and trachyte have enriched whole-rock Sr-Nd-Hf and zircon Hf isotopic compositions and mantle-like δ~(18)O values, suggesting that they were derived from low-degree partial melting of an isotopically enriched lithospheric mantle source. In contrast, the subalkaline trachyandesite and andesite have relatively depleted isotopic compositions with zircon ε_(Hf)(t) values up to +5.2 and heavy zircon O isotopic compositions with δ~(18)O values of +8.1‰ to +9.0‰, indicating that they were originated from a lithospheric mantle source that had been metasomatized by melts/fluids derived from the recycled low-T altered oceanic basalt. All of these geochemical features suggest that the Early Cretaceous volcanic rocks in the Liaodong-Jinan region would result from mixing of mafic magmas with different compositions. Such magmas were originated from the enriched lithospheric mantle and the young metasomatized mantle, respectively, with variable extents of enrichment and depletion in trace elements, radiogenic isotopes and O isotopes. Importantly, the identification of the low-T altered oceanic crust component in the origin of Early Cretaceous volcanic rocks by the zircon Hf-O isotopes provides affirmative isotopic evidence and direct material records for Mesozoic subduction of the Paleo-Pacific slab that induced decratonization of the North China Craton.     

Geochemical magma type discrimination: application to altered and metamorphosed basic igneous rocks

Five minor and trace elements, known to be chemically stable during alteration and metamorphism, have been combined in a set of binary diagrams that distinguish fresh tholeiites from alkali basalts. Of the five elements: Ti, P, Zr, Y, Nb, only P shows slight mobility during metamorphism, which is not sufficient to alter greatly the point distribution on the binary diagrams. Using these stable elements altered basaltic rocks: greenstones, spilites and amphibolites may be distinguished in the same way as fresh basalts, and their original magma may be identified as tholeiitic or alkaline basalt. All five elements are readily and rapidly determined, using XRF, thus this method may be applied as a rapid, easy way of discriminating the magma types of altered basaltic rocks. Using this method it can be demonstrated that alkali basalt magma was produced in minor quantities in the Precambrian.     

Geochemistry of basalts from central and southern New Hebrides arc: implication for their source rock composition

The basaltic rocks from the central and southern islands of the New Hebrides-Aneityum, Tanna, Erromango, Efate, Emae, Tongoa and Epi, have geochemical features typical of island arc volcanics. They are enriched in LILE and depleted in Zr, Hf, Nb and Ta compared to N-type MORB. The rocks were derived from a similar upper mantle source as N-type MORB but with a higher degree of partial melting. In addition their source was enriched in LILE (K, Rb, Sr, Ba and LREE) probably by migrating hydrous fluids released during the dehydration of the subducted oceanic slab. The basalts from Futuna island which is located farther from the trench, display characteristics typical of calc-alkaline rocks. The Futuna basalts were generated from a different LILE-enriched upper mantle source. It seems that this upper mantle source was modified by interaction with partial melts from the subducted oceanic lithosphere.     

A petrologic model for the constitution of the upper mantle and crust of the Koolau shield,Oahu, Hawaii,and Hawaiian magmatism

A petrological model for the uppermost upper mantle and crust under the Koolau shield to a depth of about 60 km has been derived on the basis of petrology of the upper mantle and crustal xenoliths in nephelinites of the Honolulu Volcanic Series. Three main xenolith suites exist in the Koolau shield: dunites, spinel lherzolites, and garnet-bearing pyroxenites. On the basis of mineralogy, it is inferred that the dunites represent cumulates in shallow crustal tholeiitic magma chambers, the spinel lherzolites form a thick (～ 40 km) layer in the upper mantle, and the garnet pyroxenite suite occurs as veins and stringers in the spinel lherzolites at about 60 km depth.The eruption sequence in a Hawaiian volcano, i.e., tholeiite → transitional basalt → alkali basalt, is generated by partial melting of a volatile-bearing garnet-lherzolite part of a lithospheric plate as it rides over a hot spot. If the tholeiite, transitional, and alkali basalts of Hawaiian volcanoes are generated at the same depth, then the observed sequence of lavas requires replenishment of the source area with volatiles and gradual decrease of the degree of partial melting with time. Post-erosional olivine nephelinites are produced from isotopically distinct, deeper source area, which may be the asthenosphere.     

Temporal change in chemistry of magma source under Central Kyushu,Southwest Japan: progressive contamination of mantle wedge

Volcanism related to subduction of the Philippine Sea (PHS) plate began in Central Kyushu at 5 Ma, after a pause of igneous activity lasting about 10 m.y. It formed a large volcano-tectonic depression, the Hohi volcanic zone (HVZ), and has continued to the present at a decreasing eruption rate. The products are largely andesite and dacite, which became enriched in K with time. The proportion of tholeiitic to calc alkalic rocks also increases with time. Calc-alkalic high-Mg basaltic andesites (YbBs) were erupted in the early stage of the HVZ activity (5–3 Ma), and high-alumina basalts (KjBs) were erupted in the later stage (2–0 Ma). In contrast to the basalts in the HVZ, Northwest Kyushu basalts (NWKBs) have been erupted on the backarc side of the HVZ since 11 Ma, and hence are not related to the PHS plate subduction. They are mainly high-alkali tholeiitic to alkali basalt that shows no notable chemical change with time. NWKB, YbB, and KjB have MORB-normalized incompatible-element spectra that differ from each other, as is well expressed in both Nb and Sr anomalies. The patterns of KjB and NWKB are typical of those for island-arc basalt (IAB) and ocean-island basalt (OIB), respectively. YbB shows a pattern intermediate between the two. We suggest that the magma source beneath the HVZ changed in composition from an OIB-type mantle to an IAB-type mantle as the subduction of PHS plate advanced. However, the magma source remained fertile under Northwest Kyushu. In order to explain the temporal change of source mantle beneath the HVZ, we propose a model for progressive contamination of the mantle wedge, in which three processes (contamination by a slab-derived component, subtraction of magma from the mantle, and mixing of the mantle residue and slab-derived component) are repeated as subduction continues. As long as the progressive contamination of mantle wedge proceeds, its trace-element composition converges at a steady-state value for a short period. This value does not depend on the initial composition of the mantle wedge but instead on the composition of the slab-derived component. The trace-element composition of the magma produced in such a mantle wedge approaches that of the slab-derived component with time, but the major-element composition is determined by the phase relations of mantle peridotite. The slab-derived component may be basaltic liquid that is partially melted from rutile-bearing eclogite.