Petrology and geochemistry of potassic rocks in the Gölcük area (Isparta, SW Turkey): genesis of enriched alkaline magmas

The Lower Pliocene volcanic rocks occurring in the Gölcük area of SW Turkey exhibit alkaline major element trends with a general potassic character. The development of volcanism can be divided into 2 major stages such as trachytic ancient lavas/domes and tephriphonolitic, trachyandesitic to trachytic Gölcük eruptions (ignimbrites, lava/dome extrusions, phreatomagmatic deposits, and finally, young domes). Volcanic rocks consist primarily of plagioclase, clinopyroxene (which ranges in composition from diopside to augite and are commonly zoned), biotite, and phlogopite. Amphibole phenocrysts are restricted to the pyroclastic deposits. Pseudoleucites are also seen only in the lava/dome extrusions. Oxides and apatites are common accessory phenocryst phases. As would be expected from their potassic–alkaline nature, the volcanic rocks of the Gölcük area contain high amounts of LILE (Ba, Sr, Rb and K), LREE, and Zr. Concentrations of compatible elements such as Cr, Ni and V are very low, possibly indicating fractionation of olivine and clinopyroxene. Correlation of SiO₂, Rb/Sr and MgO with ⁸⁷Sr/⁸⁶Sr (0.703506–0.704142) exhibit an increasing trend in the direction of crustal contamination. However, the isotopic compositions of Sr are not as high to indicate a high level of crustal contamination. Geochemical data are consistent with the derivation of Gölcük volcanic rocks from a metasomatized and/or enriched lithospheric mantle source during crustal extension in the area. This metasomatism was probably occurred by fluids released from the northward subduction between African and Eurasian plates during Tertiary, as the Gölcük volcanic rocks display features of island-arc magmas with having high Ba/Nb (>28) ratios, and Nb and Ti depletions. Lower Pliocene volcanism in the Gölcük was response to extensional tectonics.     

Geochemical characteristics of Yamadağı volcanics in central east Anatolia: an example from collision-zone volcanism

Neogene Yamadağı volcanic rocks consist of basaltic trachyandesite, trachyandesite, andesite, and dacite. The major- and trace-element chemistry indicates that the lavas are dominantly calc-alkaline and mildly alkaline in character, sodic in nature, and intermediate to acidic in composition. REE and trace-element patterns of volcanic rocks are similar to those typical of within plate magmatics. Volcanic rocks have low ⁸⁷Sr/⁸⁶Sr (0.70389–0.70633) and high ¹⁴³Nd/¹⁴⁴Nd ratios (0.51267–0.51276) and mostly plot within the mantle array of the isotope ratio diagram. The linear correlations among ⁸⁷Sr/⁸⁶Sr−¹⁴³Nd/¹⁴⁴Nd, SiO₂−⁸⁷Sr/⁸⁶Sr and SiO₂−¹⁴³Nd/¹⁴⁴Nd isotope ratios in the volcanics suggest that fractional crystallization combined with minor assimilation was an important process within the collision zone.     

Cretaceous subduction-related volcanism in the northern Sanandaj-Sirjan Zone, Iran

Cretaceous volcanic rocks (SCV) are widely developed in the northern part of the Sanandaj-Sirjan Zone, northwest Iran. Based on the mineralogy, texture and geochemical composition these rocks are divided in two main groups, the first and main one situated in the central part of the study area and the second one in the northeast. The former is dominantly basalts, andesitic basalts, and andesites and the latter comprises andesite, trachy-andesite to acidic variants, with porphyritic to microlithic porphyry and vitrophyric textures. Beside the differences between these two groups, the chemical compositions all of these rocks show a calc-alkaline affinity and enrichment in LIL elements (Rb, Ba, Th, U, and Pb) and depletion in Nb, Ti, and Zr, as evident in spider diagrams normalized to primitive mantle. The rocks are particularly enriched in Rb and depleted in Nb and Ti, as well as displaying high Rb/Sr and Rb/Ba ratios and low ratios of incompatible elements such as Nb/U (<10; range, 0.6–9), Th/U (<2), and Ba/Rb (<20). The significant U enrichment relative to neighbouring Nb and Th in the mantle-normalized variation diagram is mainly a result of source enrichment by slab-derived fluids. Significantly lower Nb/U ratios are observed in arc volcanics. These low values are generally ascribed to the strong capacity of LILE and the inability to transfer significant amounts of HFSE via slab-derived hydrous fluid. The results of geochemical modelling suggest a mantle lithospheric source that was metasomatized by fluids derived from a Neo-Tethyan subducted slab during the Middle to Late Cretaceous in the northern part Sanandaj-Sirjan Zone.     

Isotopic geochemistry of Fernando de Noronha

Volcanic and hypabyssal rocks ranging in age from 12 to 3 Ma from the Fernando de Noronha archipelago in the western equatorial Atlantic Ocean can generally be divided into two age-compositional groups that have variable and distinct isotopic compositions. Predominantly older alkali basalts and trachytes are generally characterized by more radiogenic Sr-isotopic (⁸⁷Sr/⁸⁶Sr= 0.70457–0.70485) compositions and less radiogenic Nd-isotopic (¹⁴³/Nd¹⁴⁴Nd= 0.51271–0.51281) and Pb-isotopic (²⁰⁶Pb/²⁰⁴Pb= 19.132–19.282) compositions relative to the generally younger, more alkaline Si-undersaturated rocks which include nephelinites, ankaratrites, and melilitites (⁸⁷Sr/⁸⁶Sr= 0.70365–0.70418,¹⁴³Nd/¹⁴⁴Nd= 0.51277–0.51290,²⁰⁶Pb/²⁰⁴Pb= 19.317–19.565). These variations suggest the influence of at least two separate components in the source(s) of both series. One component is characterized by highRb/Sr and low μ, possibly derived from delaminated subcontinental lithosphere, whereas the other has high μ and lowRb/Sr similar to the source of St. Helena lavas. A third component is suggested by correlated compositions in the latest alkaline, Si-undersaturated lavas, and this component may be derived from depleted mantle. These isotopic variations in conjunction with the generally increasing degree of alkalinity with time are consistent with the temporal depletion of a low-μ, highRb/Sr component and increasing contributions from a high-μ component in the sources of the volanic rocks of Fernando de Noronha.     

Strontium isotopic composition and trace element data bearing on the origin of Cenozoic volcanic rocks of the central and southern Andes

The Cenozoic volcanic rocks of the southern Andes are characterized by low ⁸⁷Sr/⁸⁶Sr ratios (0.7040–0.7045), which are consistent with an origin in the downgoing slab of oceanic lithosphere or the overlying mantle. These values are distinctly lower than those from corresponding rocks of the central Andes.The calc-alkaline rocks of the central Andes exhibit higher Sr isotopic values (0.705–0.713) and variable Rb/Sr ratios. Different explanations are possible for this behaviour as well as for the positive correlation between ⁸⁷Sr/⁸⁶Sr and Rb/Sr expressed in an apparent isochron of 380 ± 50 m.y. It is postulated that these magmas result from a mixing process between a primary magma with basaltic affinities and crustal material of relatively young age.A model is proposed for the generation of the “andesitic” magmas of the central Andes by which crustal rocks of the upper part of the crust are added to the base of the crust by an accretionary process at the margin of the continent. Melts from these upper crustal rocks act as contaminants in “andesitic” magmas.The role of crustal material is still more significant in the generation of the ignimbritic magmas; they are considered to result from a two-stage melting process by which igneous rocks, belonging to a former stage of development of the Andes, are engulfed in the subduction zone, where they melt.     

Petrogenesis and geodynamic significance of the Ganhe Formation lavas,eastern Great Xing'an Range,China: Evidence from geochemistry and geochronology

Mesozoic volcanic rocks are widespread throughout the Great Xing'an Range of northeastern China. However, there has been limited investigation into the age and petrogenesis of the Mesozoic volcanics in the eastern Great Xing'an Range. According to our research, the volcanic rocks of the Dayangshu Basin, eastern Great Xing'an Range are composed mainly of trachybasalt, basaltic andesite, and basaltic trachyandesite, with minor intermediate–basic pyroclastic rocks. In this study, the geochemistry and geochronology of the Mesozoic volcanic rocks are presented in order to discuss the petrogenesis and tectonic setting of the Ganhe Formation in the Dayangshu Basin. Zircon U–Pb dating by laser ablation inductively coupled plasma–mass spectrometry indicates that the Mesozoic lavas formed during the late Early Cretaceous (114.3–108.8 Ma). This suite of rocks exhibits a range of geochemical signatures indicating subduction‐related genesis, including: (i) calc‐alkaline to high‐K calc‐alkaline major element compositions; (ii) enrichment of large ion lithophile elements (e.g. Rb, Ba, K) and light rare earth elements (LREEs/HREEs =7.33–9.85); and (iii) weak depletion in high field strength elements (e.g. Nb, Ta, Ti). Furthermore, Sr–Nd–Pb isotopic data yield initial ⁸⁷Sr/⁸⁶Sr values of 0.70450–0.70463, positive ε_Nd(t) values of +1.8 to +3.3, and a mantle‐derived lead isotope composition. Combined with the regional tectonic evolution, the results of this study suggest that the Ganhe Group lavas are derived from decompression melting of a metasomatized (enriched) lithospheric mantle, related to asthenospheric upwelling, which resulted from lithospheric mantle delamination and produced extension of the continental margin following the subduction of the Paleo‐Pacific Plate.     

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.     

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.     

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.     

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.     

Isotope geochemistry and origin of calc-alkaline lavas from a caledonian continental margin volcanic arc

Analyses for major and trace elements, including REE, and Sr, Nd and Pb isotopes are reported from a suite of Siluro-Devonian lavas from Fife, Scotland. The rocks form part of a major calc-alkaline igneous province developed on the Scottish continental margin above a WNW-dipping subduction zone. Within the small area (ca. 15 km²) considered, rock types range from primitive basalts and andesites (high Mg, Ni and Cr) to lavas more typical of modern calc-alkaline suites with less than 30 ppm Ni and Cr. There is a marked silica gap between these rocks (< 62%) and the rare rhyolites (> 74%), yet the latter can be generated by fractional crystallization from the more mafic lavas. In contrast, variation in incompatible element concentrations and ratios in the mafic lavas can not be generated by fractional crystallization processes. Increasing SiO₂ is accompanied by increasing Rb, K, Pb, U and Ba relative to Sr and high field strength elements, increasing LREE enrichment and increasing _Sr calculated at 410 Ma, and by decreasing HREE, Eu/Eu*, Sm/Nd and _Nd (410). _Nd and _Sr are roughly anticorrelated and have more radiogenic compositions than the mantle array, in common with data reported elsewhere from this part of the arc. The correlation extrapolates up to cross the mantle array within the composition field of the contemporary MORB source, and extrapolates down towards the probable compositional range of Lower Palaeozoic greywackes, which may form the uppermost 8 km of the crust, or may be supplied to the source by subduction. One sample, however, lies within the mantle array, and closely resembles lavas from northwestern parts of the arc, where a mantle source with mild time-integrated Rb/Sr and LREE enrichment has been inferred. The lavas have relatively high initial ²⁰⁷Pb/²⁰⁴Pb for their ²⁰⁶Pb/²⁰⁴Pb, a feature which has been interpreted elsewhere as the result of incorporation of a sediment component into arc magmas. The systematic changes with increasing SiO₂ in isotopic and chemical parameters can be explained by mixing of a greywacke-derived component with depleted mantle. The various possible mixing mechanisms are discussed, and it is considered most likely that mixing occurred in the mantle source through greywacke subduction. The bulk of the Rb, K, Ba and Pb in the lavas is probably recycled from the crust, whereas less than some 40% of the Sr and Nd is recycled. The calc-alkaline chemical trends are solely a function of mixing with the sediment component.     

The relationship between calc-alkaline volcanism and within-plate continental rift volcanism: evidence from Scottish Palaeozoic lavas

Lower Carboniferous lavas from the Midland Valley and adjacent regions of Scotland are mildly alkaline and intraplate in nature. The sequence is dominated by basalt and hawaiite, although mugearite, benmoreite, trachyte and rhyolite are also present. Basic volcanic rocks display the LIL element and LREE enrichment typical of intraplate alkali basalt terrains. Low initial⁸⁷Sr/⁸⁶Sr (0.7029–0.7046), high ε_Nd (−0.4 to +5.6) and moderately radiogenic²⁰⁶Pb/²⁰⁴Pb (17.77–18.89) ratios are also comparable with alkali basalts from other continental rifts and oceanic islands.When the Carboniferous lavas are compared with subduction-related lavas of Old Red Sandstone age, erupted in and around the Midland Valley ca. 50 Ma earlier (at 410 Ma) remarkable similarities are apparent. Significant overlap occurs in Nd and Pb isotopic compositions. Sr isotopic compositions are, however, more radiogenic in the older subduction-related lavas. This, combined with high K and Rb concentrations in ORS lavas may be explained by the incorporation of a sediment component derived from the subducted slab, which by Lower Carboniferous times had been lost from the mantle source region by convection. A pronounced negative Nb anomaly in the ORS subduction-related lavas may be explained by the retention of a Nb-bearing phase in the mantle during hydrous melting of the mantle wedge above the subduction zone.Allowing for the effects of the added component from the subducted slab, there appears to be no necessity to invoke separate mantle source regions for the two suites of lavas: both may have been derived from chemically similar portions of mantle. If volcanic arc lavas are derived from the mantle wedge, the implication is that such a source lies at relatively shallow depth within the upper mantle: the same may therefore apply to the Carboniferous continental rift basalts. This evidence, combined with the fact that there is no evident hot-spot trail across the Midland Valley despite a long period of within-plate volcanism and rapid plate movements during the Carboniferous, suggests that the alkali basalt magmatism is not the product of a deep-seated mantle plume. Rather, the volcanism appears to owe more to passive rifting and to diapiric upwelling from a source region within the uppermost mantle.     

Garibaldi group volcanic rocks of the salal creek area, southwestern British Columbia: Alkaline lavas on the fringe of the predominantly calc-alkaline garibaldi (cascade) volcanic arc

The Salal Creek area, at the north end of the main group of vents for the Quaternary Garibaldi (Cascade) Volcanic Belt, southwestern British Columbia, was the site of several small eruptions of mafic lava during the past 1 Ma. In contrast to the calc-alkaline character of all other parts of the Garibaldi Belt and the geographically nearly coincident Miocene and older Pemberton Volcanic Belt, the Salal Creek area Quaternary lavas are predominantly alkaline basalt and hawaiite with typical alkaline volcanic petrography, chemistry, and fractionation trends. Trace elements Ti-Zr-Y show within-plate character for the suite. As for other Garibaldi Belt volcanic rocks, Rb is low, Rb/Sr very low, and ⁸⁷Sr/⁸⁶Sr ratio is low, averaging 0.7032. The oxygen isotopic composition average, ¹⁸O = 5.9, is normal for mantle-derived volcanic rocks.This distinct change in magma type at the end of a volcanic are may be the consequence of a smaller degree of melting, melting at a slightly greater depth than calc-alkaline magma production, or a descending-plate edge effect.Ponded flows and pillow-palagonite accumulations indicate that several Salal Creek area eruptions occurred in proximity to ice which filled major valleys during pre-Wisconsin glacial periods.     

The La Breña — El Jagüey Maar Complex,Durango, Mexico: II. Petrology and geochemistry

A suite of 16 basanitic volcanic rocks, representing all stages in the evolution of the La Breña — El Jagüey (LBEJ) Maar Complex, has been studied petrographically and analyzed for mineral compositions and whole-rock major element, trace element, and Sr–Nd–Pb isotopic compositions. Two feldspathic granulite xenoliths were also studied as possible lower-crustal contaminants to the LBEJ magmas. The volcanic rocks contain the stable minerals olivine, plagioclase, augite, and titanomagnetite±ilmenite, plus a diverse suite of xenocrusts derived from disaggregation of mantle xenoliths of spinel lherzolite (olivine, orthopyroxene, spinel) and lower-crustal granulite xenoliths (plagioclase, quartz, augite, ilmenite). Late-stage interstitial melts rich in Fe and Ti migrated into vesicles in several samples, forming coarse-grained segregation vesicles that are dominated by ilmenite blades up to 2 mm long. The whole-rock elemental data are typical of intra-plate basanitic rocks, with strong enrichments in large ion lithophile elements (i.e. K, Th, U) as well as high field strength elements (i.e. Nb, Ta) relative to mid-ocean ridge basalts (MORB) and estimates of primordial mantle abundances. Mg# increased systematically with time during the evolution of the LBEJ Maar Complex, from 57.0–58.2 in the pre-maar lavas to 59.1–63.8 in the post-maar lavas. Compatible elements (Ca, Sc, Cr, Co, Ni) correlate positively with Mg#, whereas a large group of incompatible elements (Al, Na, K, P, Rb, Sr, Zr, Nb, Ba, La, Ce, Sm, Hf, Ta, Th, U) correlate negatively with Mg#. These trends can be closely reproduced by simple models of fractional crystallization, provided that the incompatible element abundances of the parental, high-Mg# magmas are allowed minor variability. All successful fractionation models demand an important role for augite, despite its presence in the LBEJ volcanic rocks as only a late-stage microphenocrystic and groundmass mineral. Minor garnet fractionation is necessary to produce depletion of heavy rare earth element (REE) abundances in the pre-maar lavas, whose REE patterns cross those for the rest of the suite. The importance of augite and garnet fractionation indicate that the differentiation of the LBEJ magmas took place within the upper mantle, a conclusion that is supported by the presence of spinel lherzolite xenoliths in magmas from all stages in the evolution of the maar complex. Isotopic data for seven LBEJ volcanic rocks show the following ranges: ⁸⁷Sr/⁸⁶Sr 0.70327–0.70347, ^Nd 4.2–5.0, ²⁰⁶Pb/²⁰⁴Pb 18.60–18.81, ²⁰⁷Pb/²⁰⁴Pb 15.58–15.65, ²⁰⁸Pb/²⁰⁴Pb 38.19–38.58. Sr-Nd values are negatively correlated and form a trend parallel to the mantle array, overlapping the field for ocean island basalts (OIB). The LBEJ rocks have similar ⁸⁷Sr/⁸⁶Sr values but lower ^Nd compared to basanitic rocks from the US Basin and Range Province (BRP). Pb isotopic ratios are positively correlated and overlap the braod fields for MORB and OIB and the small fields for Mexican ore deposits and volcanic rocks from the active subduction-related Mexican Volcanic Belt. The LBEJ rocks have slightly more radiogenic Pb than basanitic rocks from the US BRP. Despite correlations among the isotopic ratios of the LBEJ suite, none of these ratios correlate with position in the eruption sequence, Mg#, or any other compositional parameter. The two lower-crustal xenoliths have high ⁸⁷Sr/⁸⁶Sr values (0.707, 0.710) and low ^Nd (-1.5,-8.0) compared to the LBEJ volcanic rocks, but their Pb isotopic compositions are only slightly more radiogenic than the volcanic rocks. These data do not support the widely held view that the lower crust is a major reservoir of unradiogenic Pb. In order to further constrain the role played by crustal contamination in generating the isotopic diversity in the LBEJ suite, we conducted an extensive investigation of Sr–Nd–Pb isotopic ratios for scoria clasts from different levels of a single scoria-fall horizon in the pyroclastic sequence related to the formation of La Breña Maar. Our results do not support an important role for crustal contamination in the LBEJ magmas. Rather, we conclude that minor isotopic variability exists in the mantle source regions beneath the maar complex.     

A strontium isotope evolution model for cenozoic magma genesis,Estern Great Basin,U.S.A.

Cenozoic volcanism in the Great Basin is characterized by an outward migration of volcanic centers with time from a centrally located core region, a gradational decrease in the initial Sr⁸⁷/Sr⁸⁶ ratio with decreasing age and increasing distance from the core, and a progressive change from calc-alkalic core rocks to more alkalic basin margin rocks. Generally each volcanic center erupted copious silicic ignimbrites followed by small amounts of basalt and andesite. The Sr⁸²/Sr⁸⁶ ratio for old core rocks is about 0.709 and the ratio for young basin margin rocks is about 0.705. Spatially and temporally related silicic and mafic suites have essentially the same Sr⁸⁷/Sr⁸⁶ ratios. The locus of older volcanism of the core region was the intersection of a north-south trending axis of crustal extension and high heat flow with the northeast trending relic thermal ridge of the Mesozoic metamorphic hinterland of the Sevier Orogenic Belt. Derivation of the Great Basin magmas directly from mantle with modification by crustal contamination seems unlikely. Initial melting of lower crustal rocks probably occurred as a response to decrease in confining pressure related to crustal extension. Volcanism was probably also a consequence of the regional increase in the geothermal gradient that is now responsible for the high heat flow of the Basin and Range Province. High Sr isotopic ratios of the older core volcanic rocks suggests that conditions suitable for the production of silicic magmas by partial fusion of the crust reached higher levels within the crust during initial volcanism than during production of later magmas with lower isotopic ratios and more alkaline chemistry. As the Great Basin became increasingly attenuated, progressively lower portions of the crust along basin margins were exposed to conditions suitable for magma genesis. The core region became exhausted in low temperature melting components, and volcanism ceased in the core before nearby areas had completed the silicic-mafic eruption cycle leading to their own exhaustion of crustal magma sources.     

Composition of back-arc basin volcanics, Valu Fa Ridge, Lau Basin: Evidence for a slab-derived component in their mantle source

Samples dredged from 2 localities near the crest of the Valu Fa ridge, an active back-arc basin spreading centre in the Lau Basin, consist of highly vesicular lava fragments of andesitic composition. The samples are characterized by rare, euhedral An₈₅ plagioclase phenocrysts in a hypocrystalline groundmass of An₆₀ plagioclase laths, brown glass and rare subhedral clinopyroxene. Samples from within and, to a lesser extent, between the dredge hauls show remarkable isotopic and chemical homogeneity, with: ⁸⁷Sr/⁸⁶Sr − 0.70330 ± 2; ¹⁴³Nd/¹⁴⁴Nd − 0.51303 ± 2; ²⁰⁶Pb/²⁰⁴Pb − 18.65 ± 2; ²⁰⁷Pb/²⁰⁴Pb − 15.55 ± 1; ²⁰⁸Pb/²⁰⁴Pb − 38.34 ± 4; Sr − 165 ppm; Rb − 7 ppm; Cs − 0.17 ppm; K − 3300 to 4200 ppm; Ba − 96 ppm; and REE — LREE depleted with 12–18 × chondritic abundances. On Sr-Nd, Pb-Pb and Sr-Pb plots the volcanics lie just within or on the edge of the MORB fields, overlapping with island-arc volcanics from the Marianas and Tonga. Compared with MORB and ocean-island basalts, the samples show alkali-element enrichment relative to REE and higher Cs relative to Rb. The isotopic and geochemical characteristics of the Valu Fa Ridge volcanics clearly indicate a minor, but significant, slab-derived component in the back-arc basin mantle source.     

Geochemistry and tectonic setting of Tertiary volcanism in the Güvem area, Anatolia, Turkey

Detailed field mapping in the Güvem area in the Galatia province of NW Central Anatolia, Turkey, combined with K–Ar dating, has established the existence of two discrete Miocene volcanic phases, separated by a major unconformity. The magmas were erupted in a post-collisional tectonic setting and it is possible that the younger phase could be geodynamically linked to the onset of transtensional tectonics along the North Anatolian Fault zone. The Early Miocene phase (18–20 Ma; Burdigalian) is the most voluminous, comprising of over 1500 m of potassium-rich intermediate-acid magmas. In contrast, the Late Miocene volcanic phase (ca. 10 Ma; Tortonian) comprises a single 70-m-thick flow unit of alkali basalt. The major and trace element and Sr–Nd isotope compositions of the volcanics suggest that the Late Miocene basalts and the parental mafic magmas to the Early Miocene series were derived from different mantle sources. Despite showing some similarities to high-K calc-alkaline magma series from active continental margins, the Early Miocene volcanics are clearly alkaline with higher abundances of high field strength elements (Zr, Nb, Ti, Y). Crustal contamination appears to have enhanced the effects of crystal fractionation in the petrogensis of this series and some of the most silica-rich magmas may be crustal melts. The mantle source of the most primitive mafic magmas is considered to have been an asthenospheric mantle wedge modified by crustally-derived fluids rising from a Late Cretaceous–Early Tertiary Tethyan subduction zone dipping northwards beneath the Galatia province. The Late Miocene basalts, whilst still alkaline, have a Sr–Nd isotope composition indicating partial melting of a more depleted mantle source component, which most likely represents the average composition of the asthenosphere beneath the region.     

The cenozoic rhyolite-andesite association of the chilean andes

The eruption centres of late volcanism in Chile are situated in two separate areas in the northern and southern High Cordillera. In the north, the ignimbrites of the Rhyolite Formation and the rocks of the « Andesite » Formation occur in about equal proportions, and recent activity is meagre. In the south, the rocks of the « Andesite » Formation predominate, and many volcanoes are in a highly explosive phase of activity. Field relationships, petrological and geochemical data show that the rocks of both Formations are closely related to each other. There is evidence that the magmas of the Rhyolite Formation were formed by fusion of sialic material in the upper parts of the crust. The data for the volcanics of the « Andesite » Formation are inconsistent with their derivation by fractional crystallization of a basaltic parent or by direct mantle derivation involving a single stage process. The authors suggest that the « andesitic » magmas are products of a primary andesitic magma originated by partial fusion of material of the lower crust. Assuming that the « andesitic » magmas of the central parts of the Andes are derived from the upper mantle, this would mean — in the light of the Sr⁸⁷/Sr⁸⁶ data — that the upper mantle in the central region of the Andes is essentially more radiogenic than in other orogenic areas; moroever, it should be very similar in its chemical and Sr⁸⁷/Sr⁸⁶ composition to that of the lower crust.     

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.     

Geodynamic implications of deep mantle upwelling in the source of Tertiary volcanics from the Veneto region (South-Eastern Alps)

Major and trace element and Sr–Nd–Hf–Pb isotopic data for the most primitive Tertiary lavas from the Veneto region (South-Eastern Alps, Italy) show the typical features of HIMU hotspot volcanism, variably diluted by a depleted asthenospheric mantle component (⁸⁷Sr/⁸⁶Sr_i=0.70306–0.70378; _Ndi=+3.9 to +6.8; _Hfi=+6.4 to +8.1, ²⁰⁶Pb/²⁰⁴Pb_i=18.786–19.574). P-wave seismic tomography of the mantle below the Veneto region shows the presence of low-velocity anomalies at depth, which is consistent with possible upwellings of plume material. Between the depths of 100–250 km the velocity anomalies are approximately 2–2.5% slower than average, implying a temperature excess of about 220–280 K, in agreement with estimates for other mantle plumes in the world. In this context, the Veneto volcanics may represent the shallow expression of a mantle upflow. The presence of a HIMU-DM component in a collision environment has significant geodynamic implications. Slab detachment and ensuing rise of deep mantle material into the lithospheric gap is proposed to be a viable mechanism of hotspot magmatism in a subduction zone setting.