Petrogenesis and significance of the Mesozoic North Taihang complex: Major and trace element evidence

The intensive Mesozoic magmatism in the North China Craton (NCC) has drawn great attention for its particular geochemical signatures (e.g. high-K), petrogenesis and tectonic setting. The North Taihang complex represents the westernmost magmatic belt of th…     

The Matsue Formation: Evidence for gross mantle heterogeneity beneath Southwest Japan at 11 Ma

Abstract Middle Miocene basalts and basaltic andesites of the Matsue Formation outcrop within a 5 km radius of Matsue city in eastern Shimane Prefecture. Despite their limited outcrop and age (11.0 ± 1.5 Ma), they show a wide range in ⁸⁷Sr-⁸⁶Sr(0.70370–0.70593), ¹⁴³Nd-¹⁴⁴Nd(0.512904–0.512471) and large ion lithophile element (LILE) contents, but a relatively narrow range for some high field strength elements (HFSE) such as Nb and Ti. These basalts and andesites can be divided into three groups based on petrography, major element, trace element and isotope chemistry. Although one group has undergone some fractional crystallization, isotope chemistry precludes linkage of the groups by a closed-system process. Crustal contamination can explain isotope chemistry, but is not consistent with trace element variations. The most satisfactory model is eruption of two compositionally distinct magmas, with limited magma mixing and fractional crystallization. Published experimental work shows that one end-member resulted from shallow melting of upwelling mantle at ∼25 km. The simultaneous eruption of the other end member magma in the same area points towards a heterogeneous mantle. The isotopic composition of Matsue Formation basalts and andesites covers the entire range of Late Miocene mafic volcanic rocks of southwest Japan. Such gross heterogeneity developed on a local scale has implications for models that deal with regional chemical variations of mafic volcanic rocks in southwest Honshu.     

Petrogenesis of the Mesozoic intrusive rocks in the Tongling area,Anhui Province,China and their constraint on geodynamic process

TheTonglingarea,whichiscalledtheChineseCopperCapital,isoneofthemostimportantnon-ferrousmetalproducersinChina(e.g.Cu,AuandAg,especiallyCu).ManyresearchershavenotedthatthemetaldepositsarecloselyrelatedtotheMesozoicintrusiverocksinthisarea.Therefore,theTongl…     

Geochemistry and petrology of meta-igneous granulitic xenoliths in Neogene volcanic rocks of the Massif Central,France — implications for the lower crust

Meta-igneous mafic and ultramafic rocks, which constitute about 60% of the granulitic xenoliths enclosed in the Neogene alkali basalts of the Bournac pipe (French Massif Central) have well preserved magmatic trends of element variations. The meta-igneous suite was probably derived from at least two different parental magmas and it may be a part of a gabbroic complex which resembles mafic bodies associated with anorthosites. The xenoliths are also very similar to many other granulitic xenoliths and to meta-igneous mafic granulitic massifs. This indicates that the gabbroic intrusions may be widespread in the lower crust and the close association of gabbroic rocks with meta-sedimentary granulites suggests a model for the composition of the lower continental crust.     

Pb isotopes in Ascension Island rocks: oceanic origin for the gabbroic to granitic plutonic xenoliths

The Pb isotopic compositions and U and Pb concentrations of the lava series (alkali basalt to comendite) and of their plutonic xenoliths (gabbro to alkaline granite) of Ascension Island are reported. The data are used to evaluate the source of the xenoliths which formed two differentiation suites: the acidic and intermediate xenoliths together with most of the lavas on the one hand, and the gabbroic xenoliths and a basaltic tuff on the other hand. The Pb isotopic compositions imply a mantle origin for the source magmas of the xenoliths and confirm the possibility of generating granitic rocks in an oceanic environment by fractional crystallization of a mantle-derived magma whose geochemical and isotopic characteristics are comparable to the source magmas of oceanic island basalts.     

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.     

Continental basalts in the accretionary complexes of the South-west Japan Arc: Constraints from geochemical and Sr and Nd isotopic data of metadiabase

Abstract The Ryoke Belt is one of the important terranes in the South‐west Japan Arc (SJA). It consists mainly of late Cretaceous granitoid rocks, meta‐sedimentary rocks (Jurassic accretionary complexes) and mafic rocks (gabbros, metadiabases; late Permian–early Jurassic). Initial ?_Sr (+ 25– + 59) and ?_Nd (? 2.1–?5.9) values of the metadiabases cannot be explained by crustal contamination but reflect the values of the source material. These values coincide with those of island arc basalt (IAB), active continental margin basalt (ACMB) and continental flood basalt (CFB). Spiderdiagrams and trace element chemistries of the metadiabases have CFB‐signature, rather than those of either IAB or ACMB. The Sr–Nd isotope data, trace element and rare earth element chemistries of the metadiabases indicate that they result from partial melting of continental‐type lithospheric mantle. Mafic granulite xenoliths in middle Miocene volcanic rocks distributed throughout the Ryoke Belt were probably derived from relatively deep crust. Their geochemical and Sr–Nd isotopic characteristics are similar to the metadiabases. This suggests that rocks, equivalent geochemically to the metadiabases, must be widely distributed at relatively deep crustal levels beneath a part of the Ryoke Belt. The geochemical and isotopic features of the metadiabases and mafic granulites from the Ryoke Belt are quite different from those of mafic rocks from other terranes in the SJA. These results imply that the Ryoke mafic rocks (metadiabase, mafic granulite) were not transported from other terranes by crustal movement but formed in situ. Sr–Nd isotopic features of late Cretaceous granitoid rocks occurring in the western part of the Japanese Islands are coincident with those of the Ryoke mafic rocks. Such an isotopic relation between these two rocks suggests that a continental‐type lithosphere is widely represented beneath the western part of the Japanese Islands.     

Petrological feature of spinel lherzolite xenolith from Oki-Dogo Island: An implication for variety of the upper mantle peridotite beneath southwestern Japan

Abstract   Spinel lherzolite is a minor component of the deep-seated xenolith suite in the Oki-Dogo alkaline basalts, whereas other types of ultramafic (e.g. pyroxenite and dunite) and mafic (e.g. granulite and gabbro) xenoliths are abundant. All spinel lherzolite xenoliths have spinel with a low Cr number (Cr#; < 0.26). They are anhydrous and are free of modal metasomatism. Their mineral assemblages and microtextures, combined with the high NiO content in olivine, suggest that they are of residual origin. But the Mg numbers of silicate minerals are lower (e.g. down to Fo₈₆) in some spinel lherzolites than in typical upper mantle residual peridotites. The clinopyroxene in the spinel lherzolite shows U-shaped chondrite-normalized rare-earth element (REE) patterns. The abundance of Fe-rich ultramafic and mafic cumulate xenoliths in Oki-Dogo alkali basalts suggests that the later formation of those Fe-rich cumulates from alkaline magma was the cause of Fe- and light REE (LREE)-enrichment in residual peridotite. The similar REE patterns are observed in spinel peridotite xenoliths from Kurose and also in those from the South-west Japan arc, which are non-metasomatized in terms of major-element chemistry (e.g. Fo > 89), and are rarely associated with Fe-rich cumulus mafic and ultramafic xenoliths. This indicates that the LREE-enrichment in mantle rocks has been more prominent and prevalent than Fe and other major-element enrichment during the metasomatism.     

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.     

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).     

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

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

Origin and ascent history of unusually crystal-rich alkaline basaltic magmas from the western Pannonian Basin

The last eruptions of the monogenetic Bakony-Balaton Highland Volcanic Field (western Pannonian Basin, Hungary) produced unusually crystal- and xenolith-rich alkaline basalts which are unique among the alkaline basalts of the Carpathian–Pannonian Region. Similar alkaline basalts are only rarely known in other volcanic fields of the world. These special basaltic magmas fed the eruptions of two closely located volcanic centres: the Bondoró-hegy and the Füzes-tó scoria cone. Their uncommon enrichment in diverse crystals produced unique rock textures and modified original magma compositions (13.1–14.2 wt.% MgO, 459–657 ppm Cr, and 455–564 ppm Ni contents). Detailed mineral-scale textural and chemical analyses revealed that the Bondoró-hegy and Füzes-tó alkaline basaltic magmas have a complex ascent history, and that most of their minerals (～30 vol.% of the rocks) represent foreign crystals derived from different levels of the underlying lithosphere. The most abundant xenocrysts, olivine, orthopyroxene, clinopyroxene, and spinel, were incorporated from different regions and rock types of the subcontinental lithospheric mantle. Megacrysts of clinopyroxene and spinel could have originated from pegmatitic veins/sills which probably represent magmas crystallized near the crust–mantle boundary. Green clinopyroxene xenocrysts could have been derived from lower crustal mafic granulites. Minerals that crystallized in situ from the alkaline basaltic melts (olivine with Cr-spinel inclusions, clinopyroxene, plagioclase, and Fe–Ti oxides) are only represented by microphenocrysts and overgrowths on the foreign crystals. The vast amount of peridotitic (most common) and mafic granulitic materials indicates a highly effective interaction between the ascending magmas and wall rocks at lithospheric mantle and lower crustal levels. However, fragments from the middle and upper crust are absent from the studied basalts, suggesting a change in the style (and possibly rate) of magma ascent in the crust. These xenocryst- and xenolith-rich basalts yield divers tools for estimating magma ascent rate that is important for hazard forecasting in monogenetic volcanic fields. According to the estimated ascent rates, the Bondoró-hegy and Füzes-tó alkaline basaltic magmas could have reached the surface within hours to few days, similarly to the estimates for other eruptive centres in the Pannonian Basin which were fed by “normal” (crystal and xenoliths poor) alkaline basalts.     

Bimodal volcanism at the Katla subglacial caldera,Iceland: insight into the geochemistry and petrogenesis of rhyolitic magmas

The Katla subglacial caldera is one of the most active and hazardous volcanic centres in Iceland as revealed by its historical volcanic activity and recent seismic unrest and magma accumulation. A petrologic and geochemical study was carried out on a suite of mid-Pleistocene to Recent lavas and pyroclastic rocks originated from the caldera. The whole series is characterised by a bimodal composition, including Fe-Ti transitional alkali basalts and mildly alkalic rhyolites. Variations in trace-element composition amongst the basalts and rhyolites show that their chemical differentiation was mainly controlled by fractional crystallisation and possible assimilation. The petrology and chemistry of the few intermediate extrusive rocks show that they were derived from magma mingling or hybridisation. The absence of extrusive rocks of true intermediate magmatic composition and the occurrence of amphibole-bearing felsic xenoliths support the hypothesis of partial melting of the hydrated basalt crust as the main process leading to the generation of rhyolites. The ¹⁴³Nd/¹⁴⁴Nd and ⁸⁷Sr/⁸⁶Sr values of Katla volcanic rocks fit the general isotopic array defined by late Quaternary to Recent lavas from Iceland. A few rock specimens are distinguished by low ¹⁴³Nd/¹⁴⁴Nd values suggesting assimilation and mixing of much older crustal material. Despite their similar whole-rock chemical compositions, the postglacial rhyolitic extrusives differ from the felsic xenoliths by their glass composition and the absence of amphibole. This, together with the general chemical trend of volcanic glasses, indicates that the postglacial rhyolitic extrusives were probably derived by a process involving late reheating and partial melting of crustal material by intrusion of basaltic magmas.     

Geochemistry of calc-alkaline volcanic rocks from southeastern Iran (kouh-e-shahsavaran)

The Upper Tertiary to Quaternary volcanic complex of Kouh-e-Shahsavaran in southeastern Iran is composed of calc-alkaline rocks of island are type (high-alumina basalts, basic andesites, andesites and dacites) even though it was emplaced on the continental basement. The volcanic rocks of the complex are genetically related and were probably derived by low-pressure fractional crystallization of high-Al basalts. The anomalously high content of Sr in some rocks probably reflects an accumulation of plagioclase. The trace element data are consistent with the origin of the parental magma by partial melting of an “enriched” upper mantle peridotite.     

Neodymium-strontium isotopic evidence for extreme contamination in a layered basic intrusion

Neodymium and strontium isotopic analyses from the Kalka layered basic intrusion, central Australia, are arrayed parallel to the Sr-axis of a Nd-Sr isotopic correlation diagram and are removed from the normal basaltic field. Initial¹⁴³Nd/¹⁴⁴Nd ratios are almost constant and typical of continental basalts, whereas initial⁸⁷Sr/⁸⁶Sr ratios vary greatly and range to high values (0.7049–0.7088). Acidic granulites from the country rock lie upon the continuation of the Kalka trend at higher⁸⁷Sr/⁸⁶Sr ratios outlining a mixing system between granulite and normal basaltic magma. If average granulite acted as a contaminant, isotope dilution calculations show that amounts assimilated reached as high as 25%. Bulk contamination is confirmed petrologically by the abundance of orthopyroxene, particularly as basal orthopyroxenites and the restriction of olivine to less-contaminated levels. Analogies between Kalka and several other major layered intrusions, such as the Bushveld Complex, suggest that large-scale contamination was a significant aspect of their genesis.     

Geochemistry and petrogenesis of rift-related volcanic rocks from South Kivu (Zaire)

Two volcanic zones (Bukavu and Kamituga) south of Lake Kivu (southeastern Zaire) are part of the western branch of the Eastern African rift. They were formed during three volcanic cycles, one pre-rift (70-7 Ma old) and the other two syn-rift (7.8-1.9 Ma old and 14,000 y.-sub-Recent, respectively), and evolved from quartz tholeiites of the pre-rift period to alkali basalts of the rift stage. The basaltic rocks, which strongly predominate, are compositionally similar to other rift-related basalts and also to oceanic-island rocks. Most of the basalts have undergone only limited fractional crystallization (5–10%) dominated by olivine and clinopyroxene. The distinct variations of incompatible elements even in rocks of very similar major-element composition imply that the basaltic rocks were derived from a heterogeneous source by variable degrees of melting. The inferred source composition closely resembles that of metasomatized peridotite xenoliths from alkali basalts.     

Intracrustal origin of Arenal basaltic andesite in the light of solid–melt interactions and related compositional buffering

The origin of Arenal basaltic andesite can be explained in terms of fractional crystallization of a parental high-alumina basalt (HAB), which assimilates crustal rocks during its storage, ascent and evolution. Contamination of this melt by Tertiary calc-alkalic intrusives (quartz–diorite and granite, with ⁸⁷Sr/⁸⁶Sr ratios ranging 0.70381–0.70397, nearly identical with those of the Arenal lavas) occurs at upper crustal levels, following the interaction of ascending basaltic magma masses with gabbroic–anorthositic layers. Fragments of these layers are found as inclusions within Arenal lavas and tephra and may show reaction rims (1–5 mm thick, consisting of augite, hypersthene, bytownitic–anorthitic plagioclase, and granular titanomagnetite) at the gabbro–lava interface. These reaction rims indicate that complete `assimilation' was prevented since the temperature of the host basaltic magma was not high enough to melt the gabbroic materials (whose mineral phases are nearly identical to the early formed liquidus phases in the differentiating HAB). Olivine gabbros crystallized at pressure of about 5–6 kbar and equilibrated with the parental HAB at pressures of 3–6 kbar (both under anhydrous and hydrous conditions), and temperatures ranging 1000–1100°C. In particular, `deeper' interactions between the mafic inclusions and the hydrous basaltic melt (i.e., with about 3.5 wt.% H₂O) are likely to occur at 5.4 (±0.4) kbar and temperatures approaching 1100°C. The olivine gabbros are thus interpreted as cumulates which represent crystallized portions of earlier Arenal-type basalts. Some of the gabbros have been `mildly' tectonized and recrystallized to give mafic granulites that may exhibit a distinct foliation. Below Arenal volcano a zoned magma chamber evolved prior the last eruptive cycle: three distinct andesitic magma layers were produced by simple AFC of a high-alumina basalt (HAB) with assimilation of Tertiary quartz–dioritic and granitic rocks. Early erupted 1968 tephra and 1969 lavas (which represent the first two layers of the upper part of a zoned magma chamber) were produced by simple AFC, with fractionation of plagioclase, pyroxene and magnetite and concomitant assimilation of quartz–dioritic rocks. Assimilation rates were constant (r<sub>1</sub>=0.33) for a relative mass of magma remaining of 0.77–0.80, respectively. Lavas erupted around 1974 are less differentiated and represent the `primitive andesitic magma type' residing within the middle–lower part of the chamber. These lavas were also produced by simple AFC: assimilation rates and the relative mass of magma remaining increased of about 10%, respectively (r₁=0.36, and F=0.89). Ba enrichment of the above lavas is related to selective assimilation of Ba from Tertiary granitic rocks. Lava eruption occurred as a dynamic response to the intrusion of a new magma into the old reservoir. This process caused the instability of the zoned magma column inducing syneruptive mixing between portions of two contiguous magma layers (both within the column itself and at lower levels where the new basalt was intruded into the reservoir). Syneruptive mixing (mingling) within the middle–upper part of the chamber involved fractions of earlier gabbroic cumulitic materials (lavas erupted around 1970). On the contrary, within the lower part of the chamber, mixing between the intruded HAB and the residing andesitic melt was followed by simple fractional crystallization (FC) of the hybrid magma layer (lavas erupted in 1978–1980). By that time the original magma chamber was completely evacuated. Lavas erupted in 1982/1984 were thus modelled by means of `open system' AFCRE (i.e., AFC with continuous recharge of a fractionating magma batch during eruption): in this case assimilation rates were r₁=0.33 and F=0.86. Recharge rates are slightly higher than extrusion rates and may reflect differences in density (between extruded and injected magmas), together with dynamic fluctuations of these parameters during eruption. Ba and LREE (La, Ce) enrichments of these lavas can be related to selective assimilation of Tertiary granitic and quartz–dioritic rocks. Calculated contents for Zr, Y and other REE are in acceptable agreement with the observed values. It is concluded that simple AFC occurs between two distinct eruption cycles and is typical of a period of repose or mild and decreasing volcanic activity. On the contrary, magma mixing, eventually followed by fractional crystallization (FC) of the hybrid magma layer, occurs during an ongoing eruption. Open-system AFCRE is only operative when the original magma chamber has been totally replenished by the new basaltic magma, and seems a prelude to the progressive ceasing of a major eruptive cycle.     

Contribution of subducted Pacific slab to Late Cretaceous mafic magmatism in Qingdao region, China: A petrological record

Abstract The occurrence of the Pishikou mafic dike in the Qingdao region, China provides important constraints on the origin of Late Cretaceous (86–78 Ma) mafic magmatism on the eastern North China craton. The Pishikou mafic dike is distributed in the Cretaceous Laoshan granitoid body, Qingdao region and contains peridotitic and granulitic xenoliths, xenocrysts, and megacrysts. Rocks from the Pishikou mafic dike are basanites and have low SiO₂ (< 42 wt%) and Al₂O₃ (12.5 wt%) contents, and high MgO (> 8 wt%), total alkalis (Na₂O + K₂O > 4.8 wt%, Na₂O/K₂O > 1), TiO₂ (> 2.5 wt%), CaO (> 9 wt%) and P₂O₅ (> 1 wt%). In trace element abundances, they are highly enriched in large ion lithophile elements (LILEs) and light rare‐earth elements (LREEs) (ΣREE = 339–403 ppm, (La/Yb)_N = 39–42) without high field strength element (HFSE) depletion. These rocks have radiogenic Sr and Pb, and less radiogenic Nd isotopic compositions [(⁸⁷Sr/⁸⁶Sr)_i > 0.7059, εNd ≈ 2.7–3.8 (²⁰⁶Pb/²⁰⁴Pb)_i ≈ 18.0 ± 0.1]. The diagnostic elemental ratios, such as Nb/La, Nb/U, and Nb/Th, are compatible with those of mid‐oceanic ridge basalts (MORBs) and oceanic island basalts (OIBs). Therefore, the Pishikou mafic dike has a geochemical feature completely different from those of the Early Cretaceous mafic dikes from the Qingdao region, but similar to those of back‐arc basalts from the Japan Sea. This geochemical feature suggests that the Pishikou mafic dike was derived from an asthenosphere source, but contaminated by materials from the subducted Pacific slab. The discovery of this mafic dike thus provides a petrological evidence for the contribution of subducted Pacific slab to the Late Cretaceous magmatism in the Qingdao region of the eastern North China craton.     

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

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

Zircon geochronology and geochemistry of mafic xenoliths from Liaoning kimberlites:Track the early evolution of the lower crust,North China Craton

Since the formation of the primal nucleus at 3.8Ga[1], the North China had underwent the multi-cycle geologic processes such as arc accretion[2—4] andrift[5—7], and finally accomplished the craton[8] aroundat 1.8 Ga[2,3,9]. Paleozoic Fuxian kimberlites (LiaoningProvince) contain not only abundant peridotitic butalso mafic xenoliths. The investigation on peridotiticxenoliths indicted that the North China Craton hadcold and thick lithospheric root in the middle Ordovi-cian. The deep part o…