Garnet clinopyroxenite xenolith from Dish Hill,California

A single garnet clinopyroxenite xenolith found at the Dish Hill basanite cone near Ludlow, California, has well developed unmixing and reaction textures like those found in garnet pyroxenite inclusions in Hawaiian, African and Australian basalts and like those of pyroxenites in some European alpine peridotites. Reconstructed pyroxene compositions suggest that before unmixing the rock consisted of clinopyroxene and about 10% garnet plus spinel, but all of the garnet may have been dissolved in clinopyroxene. Most or all of the garnet formed by exsolution from clinopyroxene and by reaction between clinopyroxene and spinel in an open system. Following exsolution, the rock was deformed and partly recrystallized in the solid state. Similarity of compositions of exsolved and recrystallized minerals suggests recrystallization at P-T conditions similar to those of exsolution.The rock is not the chemical equivalent of the host basanite and cannot represent magma of basanitic composition crystallized in the mantle. Its history of deformation and recrystallization, like that of accompanying spinel lherzolite inclusions, supports the idea that the garnet clinopyroxenite is an accidental inclusion derived from the upper mantle.     

Geodynamic significance of ultramafic xenoliths from Eastern Serbia: Relics of sub-arc oceanic mantle?

A suite of highly depleted peridotite xenoliths in East Serbian Palaeogene basanites represents the lithospheric mantle beneath the Balkan Peninsula. The xenoliths are harzburgites, clinopyroxene-poor lherzolites and rare dunites. They contain mostly <5 vol.% of modal clinopyroxene and are characterized by high Mg# in silicates (>91), high Cr# in spinel (mostly 0.5–0.7), and by distinctively low Al₂O₃ contents in orthopyroxene (mostly 1–2 wt.%). They have experienced some mantle metasomatism which has slightly obscured their original composition. Nevertheless, the general characteristics of the xenoliths imply a composition which is significantly more depleted than most non-cratonic sub-continental mantle xenolith suites, as well as orogenic peridotites and abyssal peridotites. Geological and compositional evidence suggests that the xenoliths do not represent Archean mantle. The existence of Proterozoic mantle cannot be entirely excluded, although it is in disagreement with geological evidence. On the other hand, the studied xenoliths are compositionally very similar to peridotites of modern oceanic sub-arc settings. The existence of such a depleted lithospheric mantle segment is also inferred from the presence of rare orthopyroxene-rich xenoliths in the same suite. These are interpreted to have originated as lithospheric precipitates of high-Mg, SiO₂-saturated magmas that require a highly depleted mantle source. Such source is typically required by boninitic-like magmas of intraoceanic suprasubduction settings. A proposed geodynamic model to explain these observations involves accretion or underplating of the lower parts of the Tethyan oceanic lithosphere during the Upper Jurassic closure of the eastern branch of the Vardar ocean.     

Petrology of ultramafic and mafic xenoliths in picrite of Kahoolawe Island,Hawaii

A picrite lava (22 wt% MgO; 35 vol.% ol) along the western shore of the1.3–1.4 Ma Kahoolawe tholeiitic shield, Hawaii, contains small xenoliths of harzburgite, lherzolite, norite, and wehrlite. The various rock types have textures where either orthopyroxene, clinopyroxene, or plagioclase is in a poikilitic relationship with olivine. The Mg#s of the olivine, orthopyroxene, and clinopyroxene in this xenolith suite range between 86 and 82; spinel Mg#s range from 60 to 49, and plagioclase is An_75–80. A ⁸⁷Sr/⁸⁶Sr ratio for one ol-norite xenolith is 0.70444. In comparison, the host picrite has olivine phenocrysts with an average Mg# of 86.2 (range 87.5–84.5), and a whole-rock ⁸⁷Sr/⁸⁶Sr ratio of 0.70426. Textural and isotopic information together with mineral compositions indicate that the xenoliths are related to Kahoolawe tholeiitic magmatism, but are not crystallization products of the magma represented by their host picrite. Rather, the xenoliths are crystalline products of earlier primitive liquids (FeO/MgO ranging 1 to 1.3) at 5–9 kbar in the cumulate environment of a magma reservoir or conduit system. The presence of ultramafic xenoliths in picrite but not in typical Kahoolawe tholeiitic lava (6–9 wt% MgO) is consistent with replenishment of reservoirs by dense Mg-rich magma emplaced beneath resident, less dense tholeiitic magma. Mg-rich magmas have proximity to reservoir cumulate zones and are therefore more likely than fractionated residual liquids to entrain fragments of cumulate rock.     

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.     

O/O ratios in anhydrous spinel lherzolite xenoliths from the Shavaryn-Tsaram volcano, Mongolia

Anhydrous spinel lherzolite xenoliths from the Shavaryn-Tsaram volcano, which represent unusually clinopyroxenerich samples of upper mantle beneath the Tariat Depression in north-central Mongolia, have particularly low δ¹⁸O values of +4.9 to +5.7‰ SMOW. Constituent minerals exhibit small (ca. 0.5–0.7‰) variations in¹⁸O content (olivine = +4.6 to +5.3‰, clinopyroxene = +5.6 to +6.1‰, orthopyroxene = +5.8 to +6.5‰), that are unrelated to xenolith modal mineralogy, chemical composition, radiogenic isotope character, or pyroxene equilibration temperature. This O-isotope character of the Tariat xenoliths is interpreted to reflect the closed-system distribution of oxygen isotopes in a slowly cooling mantle diapir emplaced into the lithosphere from a relatively primitive region of the asthenosphere.     

Mineral chemistry of spinel peridotite xenoliths from Baengnyeong Island, South Korea, and its implications for the paleogeotherm of the uppermost mantle

Abstract   The mantle-derived xenoliths entrained in the Pliocene basanite from Baengnyeong Island, South Korea, are spinel lherzolites and spinel harzburgites. The overall compositional range of the Baengnyeong xenoliths matches that of the post-Archean xenoliths of lithospheric mantle origin from eastern China, but without any compositional evidence for a refractory Archean mantle root. Mineral compositions of the xenoliths have been used to estimate the equilibrium temperatures and pressures, and to construct a paleogeothermal gradient of the source region. The xenolith-derived paleogeotherm is constrained from about 820°C at 7.3 kbar to 1000°C at 20.6 kbar. Like those from the post-Archean Chinese xenoliths of lithospheric mantle origin, the Baengnyeong geotherm is considerably elevated relative to the conductive models at the depth of the crust–mantle boundary, reflecting a thermal perturbation probably related to lithospheric thinning. There is no significant P / T difference between harzburgite and lherzolite, which suggests that the harzburgites are interlayered with lherzolites within the depth interval beneath Baengnyeong Island.     

Distribution of trace elements in spinel and garnet peridotites

The distribution of trace elements in the upper mantle has been discussed on the basis of the trace element abundances in bulk rocks and constituent minerals of two spinel and garnet facies peridotite xenoliths in alkali basalts from eastern China. The data presented are consistent with the suggestion that highly incompatible elements (Rb, Ba, Th, U, Sr, Nb, Ta) mainly reside in intergranular components, and to a lesser extent in fluid inclusions in minerals. The LILE composition in olivine and orthopyroxene can be seriously affected by the presence of fluid inclusions. Consequently the subsolidus partitioning of the LILE cannot be used to infer the olivine-melt and orthopyroxene-melt partition coefficients for these elements. There is a significant difference in (Opx/Cpx)_HREE ratios for spinel and garnet peridotites, suggesting a P-T control on equilibrium partition coefficients.     

Rb-Sr isotope geochemistry of lherzolites and their constituent minerals from Victoria,Australia

Major element data and Rb, Sr and⁸⁷Sr/⁸⁶Sr analyses for seven spinel lherzolite xenoliths and their Recent host basalt from Victoria, Australia, are presented. The exotic nature of the xenoliths is indicated by a wide spread in⁸⁷Sr/⁸⁶Sr values (0.7035–0.7076) compared with the basalt (0.7041). Five of the lherzolites provide evidence of a thermal event in the mantle 650 m.y. ago. Equilibration temperatures calculated from the compositions of the lherzolite phases (ca. 1050°C) apparently relate to this event. Estimates of the local geothermal gradient suggest temperatures of less than 700°C in the source region before eruption of the lherzolites.Isotopic analyses of the lherzolite minerals show that orthopyroxene contains more radiogenic Sr than coexisting olivine and clinopyroxene in three of the xenoliths. The⁸⁷Sr/⁸⁶Sr relationships between clinopyroxene and orthopyroxene suggest that internal isotopic disequilibrium has existed in the source region for up to 550 m.y.     

Ancient lithospheric lherzolite xenolith in alkali basalt from Baja California

K, Rb, Sr contents and Sr isotopic composition are reported for (1) the coexisting silicate minerals of a spinel lherzolite xenolith, (2) the whole rock xenolith, and (3) the host alkali basalt from the Pleistocene-Recent San Quintin volcanic field in Baja California. The data also include major element chemistry of the four mineral phases of the xenolith. The olivine-spinel and pyroxene thermometers indicate that the last temperature of equilibration of the xenolith in the upper mantle was about 1100°C.K, Rb, and Sr abundances are extremely low in the minerals of the xenolith, in contrast with the general enrichment of Ca, Al, Fe and Na in the whole xenolith. Furthermore, the abundance levels and the⁸⁷Sr/⁸⁶Sr ratios of the minerals are greatly lowered by surface washing of the minerals in2N cold HCl for three minutes. It is suggested that this is due to grain boundary and surface contamination of the minerals which took place in the upper mantle by a vapor phase deposition, prior to the inclusion of the xenolith in the basalt. The source of the vapor phase must have a⁸⁷Sr/⁸⁶Sr ratio greater than 0.7070, the highest measured ratio in the unwashed orthopyroxene. Sr in the host alkali basalt has a⁸⁷Sr/⁸⁶Sr ratio of 0.7031, unrelated to the grain boundary material.The acid-washed minerals, the unwashed minerals and the acid-washed whole rock xenolith show a scatter on a⁸⁷Rb/⁸⁶Sr versus⁸⁷Sr/⁸⁶Sr diagram. However, the surface-washed minerals and the whole rock alone define a straight-line relationship with a positive slope, which corresponds to an age3.4 ± 0.3AE(2σ) for the rock and an initial⁸⁷Sr/⁸⁶Sr of0.70057 ± 0.0004 (2σ). The age of 3.4 AE for the lherzolite is interpreted as its last involvement in a small degree of partial melting and the consequent extreme depletion of the large ion lithophile elements from the constituent minerals.     

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

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

Structure and development of the lower crust and upper mantle of Southwestern Japan: Evidence from petrology of deep-seated xenoliths

Abstract Basic and ultrabasic xenoliths included in Cenozoic alkali basalts from the Kibi and Sera plateaus, Southwest Japan, can be classified into five groups on the basis of mineral association and texture. Their equilibration P-T conditions estimated from paragenesis and mineral chemistry indicate that the dominant rock type from the lower crust to upper mantle changes with increasing depth as follows: (i) pyroxene granulite (Group V) and meta-sediments; (ii) garnet gabbro (Group 111) and corundum anorthosite (Group IV); (iii) spinel pyroxenite (Group 11); and (iv) spinel peridotite and pyroxenite (Group I). Groups I1 and I11 show a lower degree of recrystallization than Groups I and V, and have similarities in composition and mineral chemistry to host basalts. Based on these facts along with the P-T conditions of equilibration, Groups I1 and I11 are interpreted as formed from basaltic magma that intruded beneath the crust-mantle boundary at an early stage of the magmatism of the alkali basalts, where the lower crust and uppermost mantle had consisted of Group V and metasediments, and Group I, respectively. It follows that the crust has grown downward due to underplating of basaltic magma beneath the bottom of pre-existing crust. Group IV has commonly the same mineral assemblage, corundum + calcic plagioclase + aluminous spinel, and shows locally, nearby kyanite crystals, almost the same texture as fine-grained aggregates in a quartzite xenolith. The aggregates appear to have been formed by reaction between kyanite and host basalt, and accordingly Group IV is interpreted as formed by reaction between metasediments and basaltic magma at the time of the underplating. The Kibi, Sera and Tsuyama areas are distinguished from the areas nearby the Sea of Japan by the occurrence of the garnet gabbro and corundum anorthosite xenoliths, by the absence of the association of olivine + plagioclase in basic and ultrabasic xenoliths, and by the lower temperature of equilibration of basic xenoliths. From these facts it is stressed that in general the crust becomes thinner and geothermal gradient becomes higher towards the back-arc side. Such a regional variation in crustal structure must reflect the tectonic situation of Southwest Japan at the time of the magmatism of the alkali basalts, namely rifting and shallow-level magmatism at the back-arc side.     

Characteristics of subcontinental lithospheric mantle beneath Baegryeong Island, Korea: Spinel peridotite xenoliths

Abstract   Geochemical data on Baegryeong Island spinel peridotites found in Miocene alkali basalt provide the information for lithosphere composition, chemical processes, equilibrium pressure and temperature conditions. Spinel peridotite xenoliths, showing transitional textures between protogranular and porpyroclastic textures, were accidentally trapped by the ascending alkali basalt magma. The xenoliths originate at depths from 50 to 70 km with a temperature range from 800 to 1100°C. The variations of modal and mineral compositions of the spinel peridotite xenoliths indicate that the xenoliths have undergone 1–10% fractional melting. The spinel peridotites from Baegryeong Island have undergone cryptic mantle metasomatism subsequent to melt extraction. Metasomatic agent of enriched spinel peridotite xenoliths was carbonatite melt.     

Melt–wall rock interaction in the mantle shown by silicate melt inclusions in peridotite xenoliths from the central Pannonian Basin (western Hungary)

In this paper we present a detailed textural and geochemical study of two equigranular textured amphibole-bearing spinel lherzolite xenoliths from Szigliget, Bakony–Balaton Highland Volcanic Field (BBHVF, western Hungary) containing abundant primary silicate melt inclusions (SMIs) in clinopyroxene rims and secondary SMIs in orthopyroxene (and rarely spinel) along healed fractures. The SMIs are dominantly composed of silicate glass and CO₂-rich bubbles. Clinopyroxene and orthopyroxene are zoned in both studied xenoliths, especially with respect to Fe, Mg, Na, and Al contents. Cores of clinopyroxenes in both xenoliths show trace element distribution close to primitive mantle. Rims of clinopyroxenes are enriched in Th, U, light rare earth elements (LREEs) and medium REEs (MREEs). Amphiboles in the Szg08 xenolith exhibit elevated Rb, Ba, Nb, Ta, LREE, and MREE contents. The composition of silicate glass in the SMIs covers a wide range from the basaltic trachyandesite and andesite to phonolitic compositions. The glasses are particularly rich in P₂O₅. Both primary and secondary SMIs are strongly enriched in incompatible trace elements (mostly U, Th, La, Zr) and display a slight negative Hf anomaly. The development of zoned pyroxenes, as well as the entrapment of primary SMIs in the clinopyroxene rims, happened after partial melting and subsequent crystallization of clinopyroxenes, most probably due to an interaction between hot volatile-bearing evolved melt and mantle wall-rocks. This silicate melt filled microfractures in orthopyroxenes (and rarely spinels) resulting in secondary SMIs.     

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.     

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.     

Hawaiian xenolith populations,magma supply rates,and development of magma chambers

Hawaiian volcanoes pass through a sequence of four eruptive stages characterized by distinct lava types, magma supply rates, and xenolith populations. Magma supply rates are low in the earliest and two latest alkalic stages and high in the tholeiitic second stage. Magma storage reservoirs develop at shallow and intermediate depths as the magma supply rate increases during the earliest stage; magma in these reservoirs solidifies as the supply rate declines during the alkalic third stage. These magma storage reservoirs function as hydraulic filters and remove dense xenoliths that the ascending magma has entrained. During the earliest and latest stages, no magma storage zone exists, and mantle xenoliths of lherzolite are carried to the surface in primitive alkalic lava. During the tholeiitic second stage, magma storage reservoirs develop and persist both at the base of the ocean crust and 3–7 km below the caldera; only xenoliths of shallow origin are carried to the surface by differentiated lava. During the alkalic third stage, magma in the shallow subcaldera reservoir solidifies, and crustal xenoliths, including oceanic-crustal rocks, are carried to the surface in lava that fractionates in an intermediate-depth reservoir. Worldwide xenolith populations in tholeiitic and alkalic lava may reflect the presence or absence of subvolcanic magma storage reservoirs.     

Life-time of a stratified magma chamber recorded in ultramafic xenoliths from Ichinomegata volcano,northeastern Japan

Variations in major-element chemistry and modal compositions of the mantle xenolith-bearing calc-alkalic ejecta from Ichinomegata volcano are inferred to be due to mixing of three magmatic end members: Basalt I (SiO₂ 51 wt% , MgO 8.5 wt%), Basalt II (SiO₂ 54 wt%, MgO 5 wt%), and Dacite (SiO₂ 65 wt%, MgO₂ wt%). Ultramafic xenoliths are found in mafic mixtures of Dacite-Basalt I and Dacite-Basalt II. The thermal histories of the xenoliths in both mixtures are compared with each other. Chemical compositions of olivine and orthopyroxene in xenoliths suggest that xenoliths in Basalt I were equilibrated at about 800 °C, while those in Basalt II were also equilibrated originally at about 800 °C but were subsequently annealed at about 1000 °C for more than 10^2–3 years prior to the eruption.The chemical composition of Basalt I indicates that it can coexist with upper mantle peridotite and it is an appropriate candidate for a carrier of ultramafic xenoliths from the upper mantle. On the other hand, Basalt II is fractionated and it cannot be directly derived from the upper mantle. Two pulses of xenolith-bearing basalt injection into a dacite magma chamber are inferred to have occurred. The first injection did not lead to eruption and subsequently formed a dacite/basalt stratified magma chamber. In the lower layer, the basalt was slightly differentiated to become Basalt II and ultramafic xenoliths carried by the first pulse were annealed at the bottom of the layer. The duration of the annealing of the xenoliths implies a minimum life-time of the Dacite-Basalt II stratification in the magma chamber beneath Ichinomegata of 10^2–3 years. The second injection of the xenolith-bearing basalt (Basalt I) was immediately followed by eruption, and all the magmas were effused with mixing in a conduit. Consequently, the ultramafic xenoliths carried by the second pulse are not annealed.     

Petrogenesis of anhydrous clinopyroxenite xenoliths and clinopyroxene megacrysts in alkali basalts from the Ganseong area of South Korea

Late Cenozoic alkali basalts in the Ganseong area of South Korea contain abundant ultramafic xenoliths and clinopyroxene megacrysts. Anhydrous clinopyroxene‐rich wehrlite–clinopyroxenites make up the majority of the xenolith population and range from wehrlite through olivine clinopyroxenite to clinopyroxenite. This study investigates the petrogenesis of wehrlite–clinopyroxenite xenoliths and clinopyroxene megacrysts on the basis of petrography and mineral and whole‐rock chemistry. Observations such as an absence of carbonate or apatite, high Ti/Eu ratio, and clinopyroxene‐dominated mineralogy lead us to rule out peridotite–melt reactions as the origin of the Ganseong wehrlites– olivine clinopyroxenites. The whole‐rock compositions (e.g. high abundance of CaO at a given MgO content and low abundance of incompatible elements, such as U, K, P, and Ti compared with mafic melts) indicate that the pyroxenites do not represent crystallized magma itself, but are rather cumulates with a small amount of residual liquid. Anhydrous and orthopyroxene‐free mineral assemblages, crystallization sequence of olivine→clinopyroxene→plagioclase, and mineral chemistries (e.g. low Cr# and high TiO₂ abundances in spinels and high TiO₂ and Na₂O abundances in clinopyroxenes at a given Mg#) suggest that relatively anhydrous intraplate alkaline basalt is the most likely candidate for the parent magma. Texture and compositions of the clinopyroxene megacrysts preclude a cognate origin via high‐pressure crystallization of the host magma. The clinopyroxene megacrysts occupy the Fe‐rich end of the compositional trends defined by wehrlite–pyroxenite clinopyroxenes. Progressive decreases in Mg# and an absence of significant compositional gaps between pyroxenite xenoliths and clinopyroxene megacrysts indicate fractionation and differentiation of a similar parental magma. We suggest that the clinopyroxene megacrysts represent fragments of pegmatitic clinopyroxenites crystallized from more advanced fractionation stages of the evolution of a series of magmatic liquids formed Ganseong wehrlite–clinopyroxenites.     

Petrological and seismic studies of the lithosphere in the earthquake swarm region Vogtland/NW Bohemia,central Europe

New petrological and geochemical data of upper mantle and lower crustal xenoliths from a Quaternary tephra deposit in Mýtina, Czech Republic, are discussed in the frame of previous geophysical results (receiver functions, reflection seismology) of the western Eger/Ohře Rift area. The Vogtland/NW Bohemia region is well known for intraplate earthquake swarms, which are usually associated with volcanic activity. As previously reported, ³He/⁴He data of CO₂ emissions in mofettes and mineral-water springs point at ongoing magmatic processes in this area. Using teleseismic P receiver functions, an approximately 40-km-wide Moho updoming (from 31 to 27 km) and indications for a seismic discontinuity at 50 to 60 km depth were observed beneath the active CO₂-degassing field. The studied xenolith suite probes a lithospheric profile within the structural and gas geochemical anomaly field of the western Eger Rift.With regard to texture, composition, p–T estimates and origin, five xenolith groups can be discriminated. Upper crustal xenoliths (quartzites, phyllites, mica schists) resemble crystalline country rocks at surface. One noritic xenolith (6 kbar, 800 °C) could represent a sample of the lower crust. Clinopyroxenites and hornblendites probably represent cumulates of the nephelinitic magma or fragments of magmatic veins. Porous wehrlites and one hornblende peridotite xenolith reflect a metasomatied upper mantle. Megacrysts of Ti-rich amphibole, olivine, clinopyroxene, and phlogopite could be fragments of pegmatitic veins or high-pressure phenocrysts. Most of the ultramafic nodules (xenoliths and megacrysts) formed at pressures between 6 and 11 kbar (22 to 38 km depth), at temperatures well above regional geotherms of the Bohemian Massif calculated from surface heat flow studies. Orthopyroxene-bearing spinel-lherzolite xenoliths were not observed. Our petrographical, geochemical, and thermobarometric results indicate a lithospheric mantle strongly altered by magmatic processes. This metasomatism can cause slower than typical uppermost-mantle seismic velocities in a greater area and might help to explain observed seismic anomalies.     

Hawaiian magma-reservoir processes as inferred from the petrology of gabbro xenoliths in basalt,Kahoolawe Island

Gabbro xenoliths in a tholeiitic lava of Kahoolawe Island, Hawaii, a 1.3–1.4 Ma shield volcano, are 1–3 cm in size and comprised of plagioclase, clinopyroxene, and orthopyroxene. Gabbro textures — while intergranular and in part subophitic-are open due to 28–48 vol.% of vesicular basalt occupying xenolith space. Vesicles in and around the xenoliths are lined or filled with rhyolitic glass (segregation vesicles). The host is evolved tholeiite (MgO 6.1 wt%) with phenocrysts, microphenocrysts, and glomerocrysts of olivine, clinopyroxene, orthopyroxene, and plagioclase, and megacrysts (1 cm) of plagioclase. The Sr-isotope ratio of one xenolith is 0.70489; the host basalt ratio is 0.70460. Xenolith isotope composition, grain resorption, and clinopyroxene (Fs_12.5–15Wo_38–35.5), orthopyroxene (Fs_19.5–24Wo_4.1), and plagioclase (An_68–65Or_0.8–1.2) compositions suggest that these gabbros crystallized from Kahoolawe tholeiitic magma of essentially the same composition as the host basalt, but pre-dating the magma represented by the host. Based on the absence of intergranular Fe–Ti oxide phases from the pl+cpx+opx assemblages, and the open, vuggy textures, we envision crystallization on a reservoir roof at temperatures >1100°C. Entrainment of gabbro assemblages and plagioclase megacrysts from a roof mush/suspension zone occurred during convection associated with replenishment of the magma reservoir. These open-textured gabbro xenoliths are therefore not fragments of preexisting coarse-grained bodies such as sills or segregation veins. Rhyolitic glass in vesicles represents a gas-effervescence filtration process that forced fractionated residual liquids from the groundmass into voids associated with the xenoliths.Sirrine Environmental Consultants, Fremont, CA 94538