Flux versus decompression melting at stratovolcanoes in southeastern Guatemala

The major and trace element geochemistry of lavas erupted from four volcanic front (VF) stratovolcanoes in southeastern Guatemala show differences in the relative importance of flux and decompression melting in a continental arc setting. The VF stratovolcanoes exhibit a wide compositional range from basalt to dacite, although modern Pacaya erupts basaltic lavas. The VF basalts have relatively low MgO contents and plot outside the field of primary arc magmas defined by melting experiments on hydrous peridotite. After subtracting the effects of the fractionation, assimilation, and alteration of some VF lavas, separate partial melting and mixing trends were identified for Agua–Pacaya and Tecuamburro–Moyuta.The distinct chemical signatures of the hemipelagic and carbonate sediments subducted off Guatemala provide constraints on material transfer processes that occurred between the slab and mantle wedge. Model fluids and melts from the subducted slab were calculated using recently published mineral–aqueous fluid partition coefficients. Wide separation of the model fluid and melt compositions on a U/La versus Ba/Th diagram creates diagnostic mixing curves with an enriched mid-ocean ridge basalt source. Fluid from mature ocean crust has high U/La, fluid from carbonate sediment has high Ba/Th, and fluid and melt from hemipelagic sediments have both high U/La and Ba/Th. In a simple single-stage model, a mantle metasomatized by fluid originating largely from the oceanic crust with only minor sediment fluid contributions best explains the overall large ion lithophile element composition of the VF lavas. (Th/Rb)_N ratios of ∼1 in the VF lavas from southeastern Guatemala require a component of sediment melting. Therefore, a more realistic two-stage model to describe the Guatemalan arc data involves an initial hemipelagic sediment melt input to the wedge followed by minor fluid additions from the oceanic crust or sediments. Correlation between measures of slab input and extent of melting in the older VF lavas from Tecuamburro and Moyuta favors flux-dominated melting near the base of the mantle wedge. In sharp contrast, the lack of a relationship between slab additions and melting in younger lavas from Agua and Pacaya volcanoes implies a significant role for decompression melting closer to the top of the wedge. In this melting scenario, the rate of crustal extension determines the extent of melting.     

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.     

Origin of volcanic rocks from Stromboli (Italy)

Quaternary volcanic rocks of Stromboli (Italy) can be divided into older calc-alkaline and younger shoshonitic series. The SiO₂ contents of the rocks range from 50% to 61% but the majority of them are basalts. The rocks show systematic variations in chemical composition which correlate with the volcanic stratigraphy, such that, at a given SiO₂ content, K and other incompatible elements such as REE increase with decreasing age. In addition, the La/Yb ratio increases while the K/Rb, K/Ba, Zr/Ce and Zr/Nb ratios decrease towards the top of the volcanic pile. On the other hand, the abundances of transition elements, V, Co, Sc and Zn, like most major elements are broadly similar in comparable rocks of different ages. It is suggested that the parent magmas were derived by partial melting from upper mantle peridotite enriched in incompatible elements by fluids released from the descending oceanic lithosphere. The temporal chemical variations may probably be related to the lengths of time during which fluids were in contact with the upper mantle source.     

Geochemistry of diverse basalt types from Loihi Seamount,Hawaii: petrogenetic implications

The wide variety of basalt types, tholeiitic to basanite, dredged from Loihi Seamount have minor and trace element abundances that are characteristic of subaerial Hawaiian basalts, thereby confirming that Loihi Seamount is a manifestation of the Hawaiian “hot spot”. Within the Loihi sample suite there are well-defined positive correlations among abundances of highly incompatible elements (P, K, Rb, Ba, Nb, light REE and Ta) and moderately incompatible elements (Sr, Ti, Zr and Hf) and between MgO, Ni and Cr. However, within the Loihi suite abundance ratios of geochemically similar elements (Zr/Hf, Nb/Ta and La/Ce) vary by factors of 1.2–1.5 and abundance ratios of highly incompatible elements such as P/Ce, P/Th, K/Rb, Ba/Th and La/Nb vary by factors of 1.2–2.5. These abundance ratios are not readily changed by different degrees of fractionation and melting. Therefore, we conclude that these samples are not genetically related by different degrees of melting of a compositionally homogeneous source.On the basis of K/P, K/Ti, P/Ce, Zr/Nb, Th/P and La/Sm abundance ratios, the twelve samples studied in detail can be divided into six geochemical groups. Samples within each group are similar in ⁸⁷Sr/⁸⁶Sr [1], and intra-group compositional variations may reflect low-pressure fractionation and different degrees of melting. In addition, crossing chondrite-normalized REE patterns within the alkalic basalt groups reflect equilibration of the magmas with garnet. In ratio-ratio plots involving abundance ratios of highly incompatible elements, e.g., La/P, Nb/P, K/P, Rb/P, Ba/P and Th/P, the geochemical groups define linear arrays suggestive of mixing. However, these data combined with the isotopic data are not consistent with two-component mixing.     

Geochemistry and petrogenesis of ophiolites from Northern Pindos (Greece)

The ophiolitic complex of Northern Pindos (Greece) contains ocean-floor basalts and low-Ti mafic rocks. The former rocks are similar to recent mid-ocean ridge basalts with a light REE depletion and a La/Yb ratio < 2. The low-Ti rocks resemble boninites in their high Mg and very low Ti and Zr contents and in their REE patterns which have convex-downwards shape with a slight light REE enrichment. However, their Zr/Ti, Ti/V and Zr/Y ratios are lower than in boninites. Both rock-types could be generated by dynamic partial melting of a rising upper mantle diapir. Slight enrichment in light REE, Sr, Rb and Ba in low-Ti rocks could be the result of either metasomatic or alteration processes. Although a subduction zone origin of the sequence is possible, the geochemical data do not necessarily imply such a setting.     

Petrogenesis of the late Cretaceous K‐rich volcanic rocks from the Central Pontide orogenic belt,North Turkey

Subduction‐related volcanic rocks are widespread in the Central Pontides of Turkey, and represented by the Hamsaros volcanic succession in the Sinop area to the north. The volcanic rocks display high‐K calc‐alkaline, shoshonitic and ultra‐K affinities. ⁴⁰Ar/³⁹Ar age data indicate that the rocks occurred during the Late Cretaceous (ca 82 Ma), and the volcanic suites were coeval. Primitive mantle‐normalized trace element patterns of all the lavas are characterized by strong enrichments in large ion lithophile elements (LILE) (Rb, Ba, K, and Sr), Th, U, Pb, and light rare earth elements (LREE; La, Ce) and prominent negative Nb, Ta, and Ti anomalies, all typical of subduction‐related lavas. There is a systematic increase in the enrichment of incompatible trace elements from the high‐K calc‐alkaline lavas through the shoshonitic to the ultra‐K lavas. In addition, the shoshonitic and ultra‐K lavas have significantly higher ⁸⁷Sr/⁸⁶Sr (0.70666–0.70834) and lower ¹⁴³Nd/¹⁴⁴Nd (0.51227–0.51236) initial ratios than coexisting high‐K calc‐alkaline lavas (⁸⁷Sr/⁸⁶Sr 0.70576–0.70613, ¹⁴³Nd/¹⁴⁴Nd 0.51245–0.51253). Geochemical and isotopic data show that the shoshonitic and ultra‐K rocks cannot be derived from the high‐K calc‐alkaline suite by any shallow level differentiation process, and point to a derivation from distinct mantle sources. The shoshonitic and ultra‐K rocks were derived from metasomatic veins related to melting of recycled subducted sediments, but the high‐K calc‐alkaline rocks from a lithospheric source metasomatized by fluids from subduction zone.     

The origin of intermediate and evolved lavas in the Marquesas archipelago: an example from Nuku Hiva island (French Polynesia)

The Nuku Hiva Pliocene island (Marquesas, French Polynesia) is composed of a large half-collapsed tholeiitic shield volcano (the Tekao edifice), the caldera of which is filled up by the younger Taiohae volcano. The latter edifice is characterised by a complex magmatic association including minor mafic lavas (olivine tholeiites, alkali basalts and basanites), abundant intermediate lavas (hawaiites with subsidiary mugearites, both covering 47% of the surface of the volcano) and lesser amount of evolved lavas (K-rich and Na-rich trachytes and minor benmoreites, covering 25% of the edifice). Most intermediate and evolved Taiohae lavas are amphibole-rich and crystallised under high oxygen fugacities. The mafic Taiohae lavas originated from lower degree of melting of mantle sources more enriched than that of the shield volcano tholeiites. We show that closed-system fractional crystallisation of the Taiohae basaltic magmas can account for the origin of Taiohae hawaiites and mugearites, provided that separation of substantial amount of amphibole and/or apatite occurred during this process. Similarly, fractionation of benmoreitic magmas involving large amounts of amphibole and mica may account for the genesis of K-rich and Na-rich trachytes, respectively. However, fractional crystallisation cannot account for the derivation of benmoreitic magmas from mugearitic ones: since, this process fails to explain the abrupt increase in K₂O from the latter to the former. In addition, the isotopic signature of trachytes and benmoreites is clearly distinct (more EM II-rich) from that of Taiohae basalts, hawaiites and mugearites. Three hypotheses could account for the genesis of benmoreitic magmas: assimilation of oceanic material with a strong EM II signature, differentiation of non-sampled mafic magmas derived from a mantle source having a EM II-rich signature and partial melting at depth of mafic material with a strong EM II signature. The oxidised character of Nuku Hiva lavas, uncommon in oceanic island settings, suggests interaction with water and/or the contribution of an oxidised (altered?) source material to their genesis.     

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.     

Oligocene crustal xenolith‐bearing alkaline basalt from Jandaq area (Central Iran): implications for magma genesis and crustal nature

The Oligocene alkaline basalts of Toveireh area (southwest of Jandaq, Central Iran) exhibit northwest–southeast to west–east exposure in northwest of the central‐east Iranian microcontinent (CEIM). These basalts are composed of olivine (Fo_70–90), clinopyroxene (diopside, augite), plagioclase (labradorite), spinel, and titanomagnetite as primary minerals and serpentine and zeolite as secondary ones. They are enriched in alkalis, TiO₂ and light rare earth elements (La/Yb = 9.64–12.68) and are characterized by enrichment in large ion lithophile elements (Cs, Rb, Ba) and high field strength elements (Nb, Ta). The geochemical features of the rocks suggest that the Toveireh alkaline basalts are derived from a moderate degree partial melting (10–20%) of a previously enriched garnet lherzolite of asthenospheric mantle. Subduction of the CEIM confining oceanic crust from the Triassic to Eocene is the reason of mantle enrichment. The studied basalts contain mafic‐ultramafic and aluminous granulitic xenoliths. The rock‐forming minerals of the mafic‐ultramafic xenoliths are Cr‐free/poor spinel, olivine, Al‐rich pyroxene, and feldspar. The aluminous granulitic xenoliths consist of an assemblage of hercynitic spinel + plagioclase (andesine–labradorite) ± corundum ± sillimanite. They show interstitial texture, which is consistent with granulite facies. They are enriched in high field strength elements (Ti, Nb and Ta), light rare earth elements (La/Yb = 37–193) and exhibit a positive Eu anomaly. These granulitic xenoliths may be Al‐saturated but Si‐undersaturated feldspar bearing restitic materials of the lower crust. The Oligocene Toveireh basaltic magma passed and entrained these xenoliths from the lower crust to the surface.     

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.     

Major and trace element and Sr–Nd isotope signatures of lavas from the Central Lau Basin: Implications for the nature and influence of subduction components in the back-arc mantle

New major and trace element and Sr–Nd isotope data are presented for basaltic glasses from active spreading centers (Central Lau Spreading Center (CLSC), Relay Zone (RZ) and Eastern Lau Spreading Center (ELSC)) in the Central Lau Basin, SW Pacific. Basaltic lavas from the Central Lau Basin are mainly tholeiitic and are broadly similar in composition to mid-ocean ridge basalts (MORB). Their generally high ⁸⁷Sr/⁸⁶Sr ratios, combined with relatively low ¹⁴³Nd/¹⁴⁴Nd ratios are more akin to MORB from the Indian rather than Pacific Ocean. In detail, the CLSC, RZ and ELSC lavas are generally more enriched in large ion lithophile elements (Rb, Ba, Sr, and K) than average normal-MORB, which suggests that the mantle beneath the Central Lau Basin was modified by subducted slab-derived components. Fluid mobile/immobile trace element and Sr – Nd isotope ratios suggest that the subduction components were essentially transferred into the mantle via hydrous fluids derived from the subducted oceanic crust; contributions coming from the subducted sediments are minor. Compared to CLSC lavas, ELSC and RZ lavas show greater enrichment in fluid mobile elements and depletion in high field strength elements, especially Nb. Thus, with increasing distance away from the arc, the influence of subduction components in the mantle source of Lau Basin lavas diminishes. The amount of hydrous fluids also influences the degree of partial melting of the mantle beneath the Central Lau Basin, and hence the degree of melting also decreases with increasing distance from the arc.     

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.     

The Hasan Dagi stratovolcano (Central Anatolia, Turkey): evolution from calc-alkaline to alkaline magmatism in a collision zone

The Hasan Dagi volcano is one of the two large Plio-Quaternary volcanoes in Cappadocia (Central Anatolia, Turkey). Three stages of edifice construction have been identified for this volcano: Paleovolcano, Mesovolcano and Neovolcano. Most samples from Hasan Dagi volcano are calc-alkaline and define an almost complete trend from basaltic andesite to rhyolite. However, the more recent (Neovolcano) mafic samples are alkaline basalts. The mineralogical and geochemical characteristics of the oldest lavas (Keçikalesi (13 Ma) and Paleo-Hasan Dagi (7 Ma)) are significantly different from those of the younger lavas (Meso- and Neo-Hasan Dagi (<1 Ma)). Calcic plagioclase and pigeonite are typically observed in these older lavas. The Paleovolcano basalts are depleted in alkalis and display a tholeiitic tendency whereas the differentiated lavas are depleted in Na₂O but enriched in K₂O compared to younger lavas. There is an evolution through time towards higher TiO₂, Fe₂O₃^*, MgO, Na₂O and K₂O and lower Al₂O₃ and SiO₂ which is reflected in the basalt compositions. All the basalts display multi-element patterns typical of continental margin magmas with a significant enrichment in LILE (K, Rb, Ba and Th) and LREE and strong (Paleovolcano) to moderate (Meso- and Neovolcano) negative Nb, Zr and Ti anomalies. However, the younger basalts are the most enriched in incompatible elements, in agreement with their alkaline affinities and do not systematically display negative HFSE anomalies. REE data suggest an hydrous amphibole-bearing crystallization history for both Meso- and Neovolcano lavas. The distinction between the older and younger lavas is also apparent in trace element ratios such as Nb/Y, Ti/Y and Th/Y. These ratios indicate the role of a subducted component±crustal contamination in the genesis of the Hasan Dagi lavas, particularly for the oldest lavas (Keçikalesi and Paleo-Hasan Dagi). The decreasing influence of this component through time, over the last 6–7 m.y., has been accompanied by an increasing contribution of melt-enriched lithosphere. Although the range of variation of Sr, Nd and Pb isotopic ratios is small (0.70457–0.70515; 0.51262–0.51273; 18.80–18.94; 15.64–15.69; 38.87–39.10), it also reflects the evolution of the magma sources through time. Indeed, the youngest (Neovolcano) and most primitive basalts display significantly lower ⁸⁷Sr/⁸⁶Sr than the Paleo- and Mesovolcano basalts, whereas the Mesovolcano basalts display more radiogenic Pb than Paleovolcano samples. Magma mixing processes between initially heterogeneous and/or variably contaminated magmas may account for the genesis of the less differentiated and intermediate lavas (48–57% SiO₂). Meso- and Neovolcano differentiated lavas (60–68% SiO₂) are either derived from the analyzed basalts or from more primitive and more depleted magmas by fractional crystallization±some crustal contamination (AFC). Furthermore, the highly differentiated samples (72–75% SiO₂) are not strongly contaminated. The strong calc-alkaline character of Hasan Dagi lavas, in the absence of contemporaneous subduction, must reflect the heritage of the early subduction of the Afro–Arabian plate under the Eurasian plate. The evolution towards alkaline compositions through time is clearly related to the development of extensional tectonics in Central Anatolia in the Late Miocene.     

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.     

Genesis of the Madang Cenozoic sodic alkaline basalt in the eastern margin of the Tibetan Plateau and its continental dynamic implications

The Madang Cenozoic sodic alkaline basalt occurred in the eastern margin of the Tibetan Plateau, where is a key tectonic transform region of Tibet, North China, and Yangtze blocks. The basalts are characterized by the variation in SiO₂=42%–51%, Na₂O/K₂O>4, belonging to the sodic alkaline basalt series. The rocks are enriched in Ba, Th, Nb, Ta, relative to a slight depletion in K, Rb in the trace and rare earth element (REE) spider diagrams that are similar to the typical oceanic island alkaline basalt. The Sr-Nd-Pb isotopic compositions suggest that they are derived from a mixed mantle reservoir. The western Qinling-Songpan tectonic region was controlled by Tibet, North China and Yangtze blocks since Cenozoic, therefore, the region was in the stage of the substance converge from the mantle to upper crust, producing a mixed mantle reservoir in the studied area. The Madang basalts occurred in the specific tectonic background, they result from partial melting of a mixed asthenospheric mantle reservoir in the western Qinling-Songpan tectonic node.

     

Discriminating assimilants and decoupling deep- vs. shallow-level crystal records at Mount Adams using 238U–230Th disequilibria and Os isotopes

A suite of 23 basaltic to dacitic lavas erupted over the last 350 kyr from the Mount Adams volcanic field has been analyzed for U–Th isotope compositions to evaluate the roles of mantle versus crustal components during magma genesis. All of the lavas have (²³⁰Th/²³⁸U) > 1 and span a large range in (²³⁰Th/²³²Th) ratios, and most basalts have higher (²³⁰Th/²³²Th) ratios than andesites and dacites. Several of the lavas contain antecrysts (crystals of pre-existing material), yet internal U–Th mineral isochrons from six of seven lavas are indistinguishable from their eruption ages. This indicates a relatively brief period of time between crystal growth and eruption for most of the phenocrysts (olivine, clinopyroxene, plagioclase, magnetite) prior to eruption. One isochron gave a crystallization age that is ~ 20–25 ka older than its corresponding eruptive age, and is interpreted to reflect mixing of older and juvenile crystals or a protracted period of magma storage in the crust. Much of the eruptive volume since 350 ka consists of lavas that have small to moderate ²³⁰Th excesses (2–16%), which are likely inherited from melting of a garnet-bearing intraplate (“OIB-like”) mantle source. Following melt generation and subsequent migration through the upper mantle, most Mt. Adams magmas interacted with young, mafic lower crust, as indicated by ¹⁸⁷Os/¹⁸⁸Os ratios that are substantially more radiogenic than the mantle or those expected via mixing of subducted material and the mantle wedge. Moreover, Os–Th isotope variations suggest that unusually large ²³⁰Th excesses (25–48%) and high ¹⁸⁷Os/¹⁸⁸Os ratios in some peripheral lavas reflect assimilation of small degree partial melts of pre-Quaternary basement that had residual garnet or Al-rich clinopyroxene. Despite the isotopic evidence for lower crustal assimilation, these processes are not generally recorded in the erupted phenocrysts, indicating that the crystal record of the deep-level ‘cryptic’ processes has been decoupled from shallow-level crystallization.     

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.     

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.     

Study on lithogeochemistry of Middle Jurassic basalts from southern China represented by the Fankeng basalts from Yongding of Fujian Province

There exists an E-W trending Middle Jurassic volcanic zone in southern China. The Fankeng basalts in the Yongding basin of Fujian Province are considered to be a typical example. The Fankeng basalts have TiO2 contents in the range of 1.92%-3.21%. They are classified as high-Ti basalts. They also have higher total Fe (averaging FeO* = 11.09%). The Middle Jurassic Fankeng basalts from southwestern Fujian have obvious distinctive lithogeochemical features from early Cre- taceous basalts from southeastern coast of China. They have higher HFSE, such as Th, Nb, Ta, Zr and Ti. Their element ratios related with HFSE, such as Zr/Ba, La/Nb, La/Ta ,Zr/Y, Ti/Y, Ba/Nb, K/Ti and Rb/Zr are similar to those of OIB. The most samples have ε Nd(T) of-0.70-0.24, which are near chondrite. Some samples have higher ε Nd(T) of 1.87-3.55.Therefore, these basaltic magmas might be derived from depleted asthenospheric mantle. The lithogeochemical characteristics of the Fankeng basalts may be caused by interaction between asthenosphere and lithosphere at the time. The (Early-) Middle Jurassic basalts and gabbros from southeastern Hunan, southern Jiangxi and northern Guangdong provinces show similar geochemical features to those of the Fankeng basalts from the Yongding of Fujian. Occurrence of these OIB-type basalts in the area may be regarded as the petrological mark of upwelling of asthenosphere at the time. Upwelling of asthenosphere has led to tectonic extension and the formation of rifted basin in the area.     

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.