Geochemistry of peridotite xenoliths in alkali basalts from Jeju Island, Korea

Abstract   Ultramafic xenoliths in alkali basalts from Jeju Island, Korea, are mostly spinel lherzolites with subordinate amounts of spinel harzburgites and pyroxenites. The compositions of major oxides and compatible to moderately incompatible elements of the Jeju peridotite xenoliths suggest that they are residues after various extents of melting. The estimated degrees of partial melting from compositionally homogeneous and unfractionated mantle to form the residual xenoliths reach 30%. However, their complex patterns of chondrite-normalized rare earth element, from light rare earth element (LREE)-depleted through spoon-shaped to LREE-enriched, reflect an additional process. Metasomatism by a small amount of melt/fluid enriched in LREE followed the former melt removal, which resulted in the enrichment of the incompatible trace elements. Sr and Nd isotopic ratios of the Jeju xenoliths display a wide scatter from depleted mid-oceanic ridge basalt (MORB)-like to near bulk-earth estimates along the MORB–oceanic island basalt (OIB) mantle array. The varieties in modal proportions of minerals, (La/Yb)_N ratio and Sr-Nd isotopes for the xenoliths demonstrate that the lithospheric mantle beneath Jeju Island is heterogeneous. The heterogeneity is a probable result of its long-term growth and enrichment history.     

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.     

Spinel peridotite xenoliths in the West Carpathian late cenozoic alkali basalts and their tectonic significance

In the Late Cenozoic West Carpatian alkali olivine basalts spinel peridotite xenoliths have been found. Their mineral composition corresponds to those found in this type of xenoliths in alkali basalts throughout the world (Mg-rich olivine, Cr-diopside, clinopyroxene, spinel). For the studied West Carpathian alkali olivine basalts kaersutite amphibole and clinopyroxene magacrysts are characteristic. The presence of the xenoliths under consideration in the boundary zone between Tatra and Pannonian blocks is the consequence of tectonic conditions (thickness of the Crust) in the area mentioned as distinct from the other West Carpathian areas of alkali olivine basalt occurrences.     

中国东部地幔岩包体的产出及其与地球内部构造的关系

中国东部橄榄岩和榴辉岩深源包体的地理分布构成了全球环太平洋深源包体分布带的重要组成部分。深源包体的产出与地球内部构造密切相关。尖晶石橄榄岩和镁铝榴石橄榄岩两种包体与上地幔的构造分带相一致,榴辉岩包体代表上地幔中局部的分凝体。碱性玄武岩浆的活动和深源岩石带的形成应为板块构造运动的结果。     

Geothermal gradient of the upper mantle beneath Jeju Island, Korea: Evidence from mantle xenoliths

Abstract Ultramafic xenoliths found in alkali basalts from Jeju Island, Korea are mostly spinel lherzolites accompanied by subordinate amount of spinel harzburgites and pyroxenites. The combination of results from a two-pyroxene geothermometer and Ca-in-olivine geobarometer yields temperature–pressure (T–P) estimates for spinel peridotites that fall in experimentally determined spinel lherzolite field in CaO-Fe-MgO-Al₂O₃-SiO₂-Cr₂O₃ (CFMASCr) system. These T–P data sets have been used to construct the Quaternary Jeju Island geotherm, which defines a locus from about 13 kbar at 880°C to 26 kbar at 1040°C. The geothermal gradient of Jeju Island is greater than that of the conventional conductive models, and may be as a result of a thermal perturbation by the heat input into the lithospheric mantle via the passage and emplacement of magma. Spinel–lherzolite is the main constituent rock-type of the lithospheric mantle beneath Jeju Island. Pyroxenites may be intercalated in peridotites at similar depth and temperature as re-equilibrated veins or lenses.     

Origin of fine‐grained peridotite xenoliths from Iraya volcano of Batan Island,Philippines: deserpentinization or metasomatism at the wedge mantle beneath an incipient arc?

Abstract Peridotite xenoliths from the subarc mantle, which have been rarely documented, are described from Iraya volcano of the Luzon arc, the Philippines, and are discussed in the context of wedge-mantle processes. They are mainly harzburgite, with subordinate dunite, and show various textures from weakly porphyroclastic (C-type) to extremely fine-grained equigranular (F-type). Textural characteristics indicate a transition from the former to the latter by recrystallization. The F-type peridotite has inclusion-rich fine-grained olivine and radially aggregated orthopyroxene, being quite different in texture from ordinary mantle-derived peridotites previously documented. Despite their strong textural contrast, the two types do not show any systematic difference in modal composition. The harzburgite of C-type has ordinary mantle peridotite mineralogy; olivine is mostly Fo91–92 and chromian spinel mostly has Cr#s (= Cr/[Cr + Al] atomic ratios) from 0.3 to 0.6. Olivine is slightly more Fe-rich (Fo89–91) and spinel is more enriched in Cr (the Cr#, 0.4–0.8) and Fe³⁺ in F-type peridotites than in C-type harzburgite. Orthopyroxene in F-type peridotites is relatively low in CaO (<1 wt%), Al₂O₃ (<2 wt%) and Cr₂O₃ (<0.4 wt%). The F-type peridotite was possibly formed from the C-type one by recrystallization including local dissolution and precipitation of orthopyroxene assisted by fluid (or melt) of subduction origin. Textural characteristics, however, indicate a deserpentinization origin from abyssal serpentinite of which protolith was a C-type peridotite. In this scenario the initial abyssal serpentinite was possibly dehydrated due to an initiation of magmatic activity beneath an incipient oceanic arc like Batan Island. The F-type peridotite is characteristic of the upper mantle of island arc, especially of incipient arc.     

Effects of melt percolation on the Re-Os systematics of continental mantle lithosphere: A case study of spinel peridotite xenoliths from Heilongjiang,NE China

Os isotope ratios of mantle peridotites have been considered to be largely immune to recent melt-rock interaction. However, Os isotope ratios and PGE (Platinum group elements) concentrations of the Yong’an xenoliths have been significantly modified by melt percolation, and are not suitable for determining the formation age of lithosphere mantle in Yong’an. In this study, the Yong’an spinel peridotite xenoliths are divided into two groups: N-Type and E-Type. The N-Type group including cpx (clinopyroxene)-poor lherzolite and harzburgite, shows a large variation of Cr#(sp) (13.2-48) and sulfur contents (from 171 ppm to below detection limit), whereas the E-Type peridotites are mainly refractory harzburgites and are characterized by high Cr#(sp) (35.3-42.2) and overall low sulfur contents (below 51 ppm). Both types show similar major and REE (rare earth element) patterns. Furthermore, the N-Type peridotites display a restricted range of iridium-group PGE (IPGE), Os/Ir and Ru/Ir ratios (Os/Ir = 0.64-1.12, Ru/Ir = 1.52-1.79) and variable palladium-group PGE (PPGE) contents (3.4-14.9 ppb), whereas the E-Type peridotites show a large variation of Os/Ir and Ru/Ir ratios (Os/Ir = 0.33-0.84, Ru/Ir = 0.94-1.6), and a restricted range of PPGE (4.3-6.9 ppb). 187Os/188Os ratios of E-Type peridotites are higher than those of N-Type peridotites at comparable fertility levels. These results suggest that N-Type peridotites may have been overprinted by metasomatism via small melt fractions, in which the percolation of the volatile-rich, small melt fractions only resulted in LILE (large ion lithophile element) enrichment of clinopyroxene, and their whole rock PGE contents and Re-Os isotope values were little changed. Moreover, E-Type peridotites may have been modified by melt-rock reaction involving relatively large melt fractions, which may result in the formation of secondary cpx and olivine and the removal of IPGE-bearing minerals such as Ru-Os-(Ir) alloys or laurite, followed by precipitation of secondary sulfides from melt with radiogenic isotopic signature.     

Asthenospheric percolation of alkaline melts beneath the St. Paul region (Central Atlantic Ocean)

Two peridotite suites collected by submersible in the equatorial Atlantic Ocean (Hekinian et al., 2000) were studied for textures, modes, and in situ major and trace element compositions in pyroxenes. Dive SP12 runs along the immersed flank of the St. Peter and Paul Rocks islets where amphibole-bearing, ultramafic mylonites enriched in alkalies and incompatible elements are exposed (Roden et al., 1984), whereas dive SP03 sampled a small intra-transform spreading centre situated about 370 km east of the St. Peter and Paul Rocks. Both suites are characterized by undeformed, coarse-grained granular textures typical of abyssal peridotites, derived from residual mantle after ～ 15% melting of a DMM source, starting in the garnet stability field. Trace element modelling, textures and lack of mineral zoning indicate that the residual peridotites were percolated, reacted and refertilized by ～ 2.6% partially aggregated melts in the uppermost level of the melting region. This relatively large amount of refertilization is in agreement with the cold and thick lithosphere inferred by previous studies. Freezing of trapped melts occurred as the peridotite entered the conductive layer, resulting in late-stage crystallization of olivine, clinopyroxene, spinel, ± plagioclase. Chondrite-normalized REE patterns in clinopyroxenes from SP03 indicate that they last equilibrated with (ultra-) depleted partial melts. In contrast, REE concentrations in clinopyroxenes from SP12 display U and S shaped LREE-enriched patterns and the calculated compositions of the impregnating melts span the compositional range of the regional basalts, which vary from normal MORB to alkali basalt sometimes modified by chromatographic fractionation with no, or very limited, mineral reaction. Thus the mylonitic band forming the St. Peter and St. Paul Rocks ridge is not a fragment of subcontinental lithospheric mantle left behind during the opening of the Central Atlantic, nor the source of the alkaline basalts as previously suggested. Rather, dive SP12 sampled residual peridotites of normal MORB mantle that were located close to channels transporting alkali basalts. Reacted melts escaping from these channels, infiltrated, and locally equilibrated with, the peridotite matrix by ion exchange reactions. Relicts of the source of the alkaline basalts were not sampled but our study suggests that it was a component of the MORB mantle underlying the St. Paul region.     

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.     

Deep melting and sodic metasomatism underneath the highly oblique-spreading Lena Trough (Arctic Ocean)

Abyssal peridotites collected along the highly oblique-spreading Lena Trough north of Greenland and Spitsbergen have mineral compositions that are similar to residual abyssal peridotites, except for high sodium concentrations in clinopyroxene (cpx). Most samples are lherzolites with light rare earth element (REE)-depleted cpx trace element patterns, but significantly fractionated middle to heavy REE ratios at relatively high heavy REE concentrations. Such characteristics can only be explained by initial melting of a garnet peridotite followed by low degrees of melting in the stability field of spinel peridotite. The residual garnet signature requires either a high potential temperature of the upwelling mantle, or elevated solidus-lowering water contents. The limited spinel field melting suggests a deep cessation of melt extraction, possibly because of the presence of a thick lithospheric cap. This is consistent with the extremely low effective spreading rate and the vicinity to a passive continental margin, which allow conductive cooling to reach deeper levels than commonly estimated for faster mid-ocean ridges. High sodium concentrations in cpx are neither explainable by melt refertilization, nor by a simple diffusion mechanism. The efficient fractionation of sodium from the light REE requires post-melting metasomatism, which is typically restricted to the subcontinental lithosphere. This might imply that the Lena Trough peridotites represent unroofed subcontinental mantle, from which no melt was extracted during the opening of the Lena Trough. It is more likely that sodic metasomatism occurred after partial melting underneath the Lena Trough, and that such an enrichment process is responsible for elevated sodium concentrations in abyssal peridotites elsewhere. Sodium in cpx of residual peridotites can therefore not serve as an indicator of partial melting or melt refertilization.     

Relation between mantle shear zone deformation and metasomatism in spinel peridotite xenoliths of Jeju Island (South Korea): Evidence from olivine CPO and trace elements

This study presents geochemical and fabric analysis of coarse-grained, porphyroclastic and mylonitic spinel peridotite xenoliths derived from the shallow subcontinental lithospheric mantle of Jeju Island (South Korea). Fabric analysis of olivines in the studied peridotites shows activation of the high temperature (0 1 0)[1 0 0] slip system; however, in the porphyroclastic and mylonitic peridotites, activation of (0 k l)[1 0 0] slip system results in a weaker fabric. Formation of porphyroclastic and mylonitic fabrics are thought to form in a shear-dominated environment. The results of the trace element analysis reveal that the smaller the grain size and weaker the fabric, the more enriched in LREE and HFSE are the peridotites, which indicates a strong relationship between metasomatic agents and mantle shear zones.     

Fractionation of platinum group elements in upper mantle: Evidence from peridotite xenoliths from Wangqing

The peridotite xenoliths from Wangqing display a downward-concave PGE pattern with Pt at maximum due to Pt-Pd fractionation, which is different from the flat or negatively sloped patterns commonly observed for worldwide peridotite xenoliths and massifs. Taking into account the difference in partition coefficients of Pt and Pd between alloy and sulfide melt, it is suggested that some of the Wangqing peridotites must have been equilibrated with a melt in which alloy and sulfide coexisted. Segregation of Pt-rich alloy from Pd-sulfide melts due to density contrast and extraction of residual melts without sulfide saturation resulted in the fractionation of Pt from Pd. Project supported by the Ministry of Human Affairs and a part of an international collaboration program between the Chinese Academy of Sciences and Centre National de Recherche Scientifique (CNRS, France), and Australian Institute of Nuclear Sciences and Engineering (AINSE) grant to SJR.     

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.     

Experimental studies of melt-peridotite reactions at 1–2 GPa and 1250–1400°C and their implications for transforming the nature of lithospheric mantle and for high-Mg signatures in adakitic rocks

Experiments of the melt-peridotite reaction at pressures of 1 and 2 GPa and temperatures of 1250–1400°C have been carried out to understand the nature of the peridotite xenoliths in the Mesozoic high-Mg diorites and basalts of the North China Craton,and further to elucidate the processes in which the Mesozoic lithospheric mantle in this region was transformed.We used Fuxin alkali basalt,Feixian alkali basalt,and Xu-Huai hornblende-garnet pyroxenite as starting materials for the reacting melts,and lherzolite xenoliths and synthesized harzburgite as starting materials for the lithospheric mantle.The experimental results indicate that:(1)the reactions between basaltic melts and lherzolite and harzburgite at 1–2 GPa and 1300–1400°C tended to dissolve pyroxene and precipitate low-Mg#olivine(Mg#=83.6–89.3),forming sequences of dunite-lherzolite(D-L)and duniteharzburgite(D-H),respectively;(2)reactions between hornblende-garnet pyroxenite and lherzolite at 1 GPa and 1250°C formed a D-H sequence,whereas reactions at 2 GPa and 1350°C formed orthopyroxenite layers and lherzolite;and(3)the reaction between a partial melt of hornblende-garnet pyroxenite and harzburgite resulted in a layer of orthopyroxenite at the boundary of the pyroxenite and harzburgite.The reacted melts have higher MgO abundances than the starting melts,demonstrating that the melt-peridotite reactions are responsible for the high-Mg#signatures of andesites or adakitic rocks.Our experimental results support the proposition that the abundant peridotite and pyroxenite xenoliths in western Shandong and the southern Taihang Mountains might have experienced multiple modifications in reaction to a variety of melts.We suggest that melt-peridotite reactions played important roles in transforming the nature of the Mesozoic lithospheric mantle in the region of the North China Craton.     

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.     

Metasomatized harzburgite xenoliths from Avacha volcano as fragments of mantle wedge of the Kamchatka arc: Implication for the metasomatic agent

Abstract   Abundant peridotite xenoliths have been found in pyroclasitics of Avacha (Avachinsky) volcano, the south Kamchatka arc, Russia. They are mostly refractory harzburgite with or without clinopyroxene: the Fo of olivine and Cr/(Cr + Al) atomic ratio of spinel range from 91 to 92 and from 0.5 to 0.7, respectively. They are metasomatized to various extents, and the metasomatic orthopyroxene has been formed at the expense of olivine. The metasomatic orthopyroxene, free of deformation and exsolution, is characterized by low contents of CaO and Cr₂O₃. The complicated way of replacement possibly indicates low viscosity of the metasomatic agent, namely hydrous fluids released from the relatively cool slab beneath the south Kamchatka arc. This is a good contrast to the north Kamchatka arc, where the slab has been hot enough to provide slab-derived melts. High content of total orthopyroxene, 40 vol% on average, in metasomatized harzburgite from Avacha suggests silica enrichment of the mantle wedge, and is equivalent to some subcratonic harzburgite. Some subcratonic harzburgites therefore could have been formed by transportation of subarc metasomatized peridotites to a deeper part of the upper mantle.     

The southeast Australian lithospheric mantle: isotopic and geochemical constraints on its growth and evolution

Trace elements and isotopic compositions of whole rocks and mineral separates are reported for 15 spinel-bearing harzburgite and lherzolite xenoliths from southeastern Australia. These samples have an exceedingly large range in isotopic compositions, with⁸⁷Sr/⁸⁶Sr ranging from 0.70248 to 0.70834 and ε_Nd values ranging from +12.7 to −6.3. This range in isotopic compositions can be found in xenoliths from a single locality. The isotopic compositions of clinopyroxene separates and their whole rocks were found to be different in some xenoliths. Samples containing small glass pockets, which replace pre-existing hydrous minerals, generally show only small differences in isotopic composition between clinopyroxene and whole rock. In a modally metasomatized peridotite, significant differences in the Sr and Nd isotopic compositions of a coexisting phlogopite-clinopyroxene pair are present. Coexisting clinopyroxenes and orthopyroxenes from an anhydrous lherzolite have Sr isotopic compositions that are significantly different (0.70248 versus 0.70314), and yield an apparent age of 625 Ma, similar to that found previously by Dasch and Green [1]. However, the Nd isotopic compositions of the clinopyroxene and orthopyroxene are identical indicating recent (within 40 Ma) re-equilibration of Nd.Sr and Nd concentrations in the whole rocks and clinopyroxenes show an excellent positive correlation, and have an average Sr/Nd ratio of 15. This ratio is similar to the primitive mantle value, as well as that found in primitive MORBs and OIBs, but is much lower than that measured in island arc basalts and what might be predicted for a subduction zone-derived fluid. This indicates that a significant proportion of the Sr and Nd in these peridotites is introduced as a basaltic melt with intraplate chemical characteristics.The isotopic compositions of the peridotites reflect long-term, small-scale heterogeneities in the continental lithospheric mantle, and are in marked contrast to the near uniform isotopic compositions of the host alkali basalts (⁸⁷Sr/⁸⁶Sr= 0.7038–0.7041andε_Nd = +3.6 to +2.9). A minimum of three evolutionary stages are identified in the growth of the continental lithospheric mantle: an early basalt depletion event, recording the initial development and stabilization of the lithospheric mantle, followed by at least two enrichment episodes. These observations are consistent with continental lithospheric mantle growth involving the underplating of refractory peridotite diapirs.     

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.     

Low water contents in pyroxenes from spinel-peridotites of the oxidized, sub-arc mantle wedge

Pyroxene water contents measured by Fourier transform infrared spectrometry for Mexican and Simcoe (WA, USA) spinel-peridotite xenoliths range from 140 to 528 ppm in clinopyroxenes and 39 to 265 ppm in orthopyroxenes. Correlations between these water contents and major-element compositional data for the pyroxenes, associated spinels, and whole-rock xenoliths demonstrate that these water contents record mantle values that have not been perturbed since the xenoliths were brought to the surface by their host magmas. Broad positive correlations of pyroxene water contents with whole-rock Al₂O₃ are consistent with water behaving as an incompatible element during peridotite melting. The main control on the range of pyroxene water contents, however, appears to be the redox state of the peridotite, because estimates of oxygen fugacity from Mössbauer (Simcoe) and microprobe data (Mexico) on spinels are negatively correlated with water contents. This is consistent with the dominant mechanism of H incorporation into pyroxene, which is dependent on the oxidation-reduction of iron. Metasomatism of sub-arc mantle-wedge peridotites by oxidized fluids or melts rising from the slab raises the oxygen fugacity of the peridotites, and where temperature is high enough, induces them to partially melt. The oxidation, in turn, lowers the solubility of water in the peridotite minerals, causing more than half of the original water to be expelled. That water enters the hydrous partial melts and these ascend through the lithosphere to feed the arc magmatic system in the upper crust. Low water contents in pyroxenes from sub-arc mantle-wedge peridotites, such as those from Simcoe and some western Mexican sites, therefore appear to be complementary to the high water contents that characterize subduction-zone magmas and fuel their explosive eruptions. An estimate of water budget in subduction zones, however, indicates that the amount of water coming from the dehydration of mantle-wedge anhydrous minerals probably accounts for less than 5% of the total water present in subduction-related magmas. The high water contents of arc magmas thus are mainly attributed to fluids or melts from the slab proper. The relatively dry sub-arc mantle wedge appears to be an effective medium through which subducted water is transported from slabs toward the surface.     

The oceanic substratum of Northern Luzon: Evidence from xenoliths within Monglo adakite (the Philippines)

Abstract   A 8.65 Ma adakitic intrusive sheet exposed near Monglo village in the Baguio District of Northern Luzon contains a suite of ultramafic and mafic xenoliths including in order of abundance: spinel dunites showing typical mantle-related textures, mineral and bulk rock compositions, and serpentinites derived from them; amphibole-rich gabbros displaying incompatible element patterns similar to those of flat or moderately enriched back-arc basin basalt magmas; and amphibolites derived from metabasalts and/or metagabbros of identical affinity. A single quartz diorite xenolith carrying a similar subduction-related geochemical signature has also been sampled. One amphibolite xenolith provided a whole-rock K–Ar age of 115.6 Ma (Barremian). We attribute the origin of this suite to the sampling by ascending adakitic magmas of a Lower Cretaceous ophiolitic complex located at a depth within the 30–35 km thick Luzon crust. It could represent an equivalent of the Isabela-Aurora and Pugo-Lepanto ophiolitic massifs exposed in Northern Luzon.