A petrogenetic study of the garnet pyroxenite enclaves in spinel peridotite,North Dabieshan,China

Recently, garnet pyroxenite enclaves within peridotites occurring near Raobazhai, Huoshan County, have been discovered. The garnet pyroxenite is small pods, decimeters in size, enclosed within intensively serpentinized peridotites. Major mineral components comprise: garnet (Prp_25–35), sodium augite (Jd_10–25) with a small amount of ilmenite. There are two stages of retrometamorphism: the retrogressive granulite facies mineral assemblage is superimposed by that of amphibolite facies. The host rocks of the garnet pyroxenite are spinel peridotites, including spinel harzburgite and lherzolite. Due to intensive serpentinitization, only 5%–40% of the relic olivine (Fo_92–93) are preserved. The orthopyroxenes are Mg-rich (En_87–93) with bending of cleavages and granulation at their margins showing intracrystalline plasticity. On the basis of garnet-clinopyroxene Fe?Mg exchange equilibrium geothermometry proposed by Ellis & Green (1979) and Krogh (1988)K _D=4.06–5.28;T=793–919°C,P=1.5 GPa are estimated for the garnet pyroxenite. It is inferred that the peridotites are mantle rocks about 60 km in depth. During the exhumation of the orogenic belt, it was tectonically emplaced into the lower crust in the solid state and then uplifted to the shallow depth. Obviously, this kind of garnet pyroxenite must be petrogenetically related to its host rock. The REE distribution pattern and the Ni?Co?Sc diagram reveal that they are chemically equivalent to the basaltic melt and ultramafic residua respectively derived from partial melting of mantle rocks.     

Petrology of the Green Knobs diatreme and implications for the upper mantle below the Colorado Plateau

Peridotite inclusions, crystal fragments, and kimberlite breccia at Green Knobs, New Mexico, have been studied to evaluate compositions and processes in the upper mantle below the Colorado Plateau. Most peridotite inclusions are spinel lherzolites and harzburgites, or their partly hydrated equivalents, in the Cr-diopside group. Orthopyroxene-rich websterites and olivine websterites comprise 3% of the peridotites and formed as cumulates. Typical anhydrous or slightly hydrated peridotites contain aluminous, calcic diopside (5–7% Al₂O₃), aluminous orthopyroxene (3–6% Al₂O₃), spinel, and olivine (near Fa₉). Geothermometers based on different mineral pairs yield temperatures from above 1100°C to below 700°C in single rocks. High values, derived from pyroxenes with included exsolution lamellae, may approximate temperatures of primary crystallization. Low values, based on olivine-spinel and olivine-clinopyroxene pairs, approach upper mantle temperatures before eruption. In rare samples, some spinel grains are rimmed by garnet while others are not rimmed; garnet formation was controlled by nucleation kinetics. About one-third of the peridotites were deformed shortly before eruption, with effects ranging from mild cataclasis to the production of ultramylonites.Discrete crystals of garnet, olivine (near Fa₈), and Cr-diopside represent garnet peridotite. Eclogites were not found. The garnet peridotite is more depleted than overlying spinel peridotite, and it is not a likely source for the minettes associated with the kimberlites.The mantle below Green Knobs consists of spinel peridotite from 45 to perhaps 60 km depth immediately underlain by more-depleted garnet peridotite. The position of the spinel-garnet transition may be fixed by kinetics. The kimberlite may have been produced when heat from ascending minette magma released volatiles from otherwise depleted garnet peridotite. Resulting gas-solid mixtures erupted along zones of deformation associated with Colorado Plateau monoclines. Sheared lherzolites formed during renewed movement along these zones.     

Experimental study of spinel-garnet phase transition in upper mantle and its significance

Experimental study of spinel-garnet phase transition was carried out using natural mineral and rock specimens from xenolith of mantle rocks in Cenozoic basalt as starting materials. From the result it was found that the condition of spinel Iherzolite-garnet Ihenolite phase transition (T = 1 100°C andP = 1.8–2.0 GPa) is consistent with theP-T equilibrium condition of the five-phase assemblage spinel/garnet Iherzolite in eastern China, suggesting that there may exist a spinel-garnet Iherzolite phase transition zone with the thickness of a few km to several ten km at the depth of 55–70 km in the continental upper mantle of eastern China. The depth of phase transition from spinel pyroxenite to garnet pyroxenite is found to be less than 55 km. Experiment results also show that water promotes metasomatism on one hand but suppresses phase transition on the other. Zoning of mineral composition was also discussed. Project supported by the National Natural Science Foundation of China.     

Mixed mantle provenance: diverse garnet compositions in polymict peridotites, Kaapvaal craton, South Africa

Garnet compositions are used to understand mantle petrogenesis and to reconstruct the lithostratigraphy of the shallow mantle (<200 km). However, garnets in polymict peridotites from the Kaapvaal craton (>2500 Ma) have a centimeter-scale elemental and stable isotopic variability suggestive of a mixed mantle provenance. The chemical heterogeneity of the garnets is similar to that reported from rocks sampled over a considerable depth and temperature range within the lower lithosphere. For example garnets found in polymict peridotites are similar to garnets found in sheared and granular peridotites, ‘cold’ and ‘hot’ lherzolites, peridotitic (P-type) diamond inclusions, and garnets from polybaric (50-200 km) peridotites (i.e. spinel, garnet and diamond facies). These data indicate that the Kaapvaal cratonic root has been disturbed by complex processes possibly associated with crack propagation and entrainment that juxtaposed garnet-bearing lithologies of diverse petrogenesis, provenance and depth. This has preserved chemical disequilibrium in the high pressure minerals in what is, in effect, a mantle breccia possibly associated with kimberlite precursors.     

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.     

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.     

Supra-subduction and mid-ocean ridge peridotites from the Piranshahr area,NW Iran

The Piranshahr metaperidotites in the northwestern end of the Zagros orogen were emplaced following the closure of the Neotethys ocean. The ophiolitic rocks were emplaced onto the passive margin of the northern edge of the Arabian plate as a result of northeastward subduction and subsequent accretion of the continental fragments. The metaperidotites have compositions ranging from low-clinopyroxene lherzolite to harzburgite and dunite. They are mantle residues with distinct geochemical signatures of both mid-ocean ridge and supra subduction zone (SSZ) affinities. The abyssal peridotites are characterized by high Al₂O₃ and Cr₂O₃ contents and low Mg-number in pyroxenes. The Cr-number in the coexisting spinel is also low. The SSZ mantle peridotites are characterized by low Al₂O₃ contents in pyroxenes as well as low Al₂O₃ and high Cr-number in spinel. Mineral chemical data indicate that the MOR- and SSZ-type peridotites are the residues from ∼15–20% and ∼30–35% of mantle melting, respectively. Considering petrography, mineralogy and textural evidence, the petrological history of the Piranshahr metaperidotites can be interpreted in three stages: mantle stable stage, serpentinization and metamorphism. The temperature conditions in the mantle are estimated using the Ca-in-orthopyroxene thermometer as 1210 ± 26 °C. The rocks have experienced serpentinization. Based on the textural observations, olivine and pyroxene transformed into lizardite and/or chrysotile with pseudomorphic textures at temperatures below 300 °C during the initial stage of serpentinization. Subsequent orogenic metamorphism affected the rocks at temperatures lower than 600 °C under lower-amphibolite facies metamorphism.     

The mineral chemistry of pyroxenite xenoliths in the volcanic rocks of Hoh Xil and their significance

The pyroxenite xenoliths in the volcanic rocks of Hoh Xil consist of clinopyroxenes and orthopyroxenes. The mineral composition of these pyroxenes is similar to that of mantle xenoliths including peridotite and pyroxenite from China and abroad, and different from that of granulites. The pyroxenes formed at 1101–1400°C (averaging 1250°C) and under 30–60 kb (averaging 46 kb). We deduced that the magma was derived from the mantle at a depth of more than 150 km, which fits in with the geophysical conclusion that the low-velocity layer existed in the mantle under 150 km.

     

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.     

Temperature and pressure condition of garnet lherzolite and websterite from west Qinling,China

The mineral thermobarometry proposed in literature is used to calculate the equilibrium temperature and pressure of garnet lherzolite and websterite xenoliths within the Cenozoic kamafugite from west Qinling, Gansu Province, China. The results show that the equilibrium temperature and pressure of garnet lherzolites and websterite and 1127–1266°C, 2.9–3.6 Gpa and 1169–1248°C, 2.8–3.2 Gpa respectively. The equilibrium peressures reach or exceed the equilibrium peressure of spinel lherzolites (2.0–3.0 GPa), and fall into the stability range of garnet peridotite. The equilibrium temperature of the xenoliths reach or exceed the ocean geotherm, identical with the melting temperature of kamafugite magma determined by experiments under the conditions of post-orogenic lithosphere extension. So the thermal state of Cenozoic mantle of the west Qinling may be fit to generate the kamafugite magmatism. The research on petrology-mineralogy and geobarothermometry of the xenoliths shows that both garnet lherzolite and websterite are mantle components of the west Qinling, and may be considered as source rocks of the Cenozoic kamafugite magma.

     

Composition,temperature, and thickness of the lithosphere of the Archean Kaapvaal craton

A new model is proposed for the structure of the Kaapvaal craton lithosphere. Based on chemical thermodynamics methods, profiles of the chemical composition, temperature, density, and S wave velocities are constructed for depths of 100–300 km. A solid-state zone of lower velocities is discovered on the S velocity profile in the depth interval 150–260 km. The temperature profiles are obtained from absolute values of P and S velocities, taking into account phase transformations, anharmonicity, and anelastic effects. The examination of the sensitivity of seismic models to the chemical composition showed that relatively small variations in the composition of South African xenoliths result in lateral temperature variations of ～200°C. Inversion of some seismic profiles (including IASP91) with a fixed bulk composition of garnet peridotites (the primitive mantle material) leads to a temperature inversion at depths of 200–250 km, which is physically meaningless. It is supposed that the temperature inversion can be removed by gradual fertilization of the mantle with depth. In this case, the craton lithosphere should be stratified in chemical composition. The depleted lithosphere composed by garnet peridotites exists to depths of 175–200 km. The lithospheric material at depths of 200–250 km is enriched in basaltoid components (FeO, Al₂O₃, and CaO) as compared with the material of garnet peridotites but is depleted in the same components as compared with the fertile substance of the underlying primitive mantle. The material composing the craton root at a depth of ～275 km does not differ in its physical and chemical characteristics from the composition of the normal mantle, and this allows one to estimate the thickness of the lithosphere at 275 km. The results of this work are compared with data of seismology, thermal investigations, and thermobarometry.     

Prograde pressure-temperature path of jadeite-bearing eclogites and associated high-pressure/low-temperature rocks from western Tianshan, northwest China

Abstract Jadeite‐bearing eclogites and associated blueschists locally crop out in a greenschist facies area at Kuldkourla, near the Akeyazhi River in the western Chinese Tianshan region, northwestern China. Garnet in these metamorphic rocks shows prograde zoning with increasing Mg and decreasing Mn from the crystal center towards the rim, and is divided into Ca‐poor/Fe‐rich core and Ca‐rich/Fe‐poor mantle parts. The garnet cores include the assemblages of (i) jadeite/omphacite (X_jd = 0.34–0.96) + barroisite/taramite; and (ii) omphacite + barroisite/pargasite, with paragonite, epidote, rutile and quartz as major phases with rare albite. The garnet mantles rarely contain inclusions of omphacite, glaucophane, epidote, rutile and quartz. Major matrix phases of the pre‐exhumation stage are omphacite, glaucophane, paragonite, rutile and quartz. These mineral parageneses give pressure (P)‐temperature (T) conditions of 0.9 GPa/390°C?1.4 GPa/560°C for the stage of the garnet core formation, 1.8 GPa/520°C for the stage of the garnet mantle formation, and 2.2 GPa/495°C‐2.4 GPa/535°C for the peak eclogite facies assemblage in the matrix. The estimated P‐T conditions and continuous changes of mineral parageneses imply a counterclockwise P‐T path which is a combination of (i) an early prograde stage of high‐pressure/low‐temperature (HP/LT) blueschist facies and/or LP/LT eclogite facies; (ii) a later prograde stage involving compression with minimal heating; and (iii) a climax‐of‐subduction stage characterized by a slight decrease of temperature with increasing pressure. The negative dP/dT of the latest subduction stage is possibly a record of the following events after a continuous subduction and ridge approach: (i) material migration within the upper part of the subducting slab, which has an inverse thermal gradient caused by ductile flow and/or slab break during subduction; and/or (ii) temporary cooling of the wedge mantle–slab interface by continuous subduction of a relatively cold slab following subduction of a hotter ridge.     

Nb/Ta,Zr/Hf and REE in the depleted mantle: implications for the differentiation history of the crust–mantle system

High-precision Nb, Ta, Zr, Hf, Sm, Nd and Lu concentration data of depleted mantle rocks from the Balmuccia peridotite complex (Ivrea Zone, Italian Alps) were determined by isotope dilution using multiple collector inductively coupled plasma mass spectrometry (MC-ICPMS) and thermal ionisation mass spectrometry (TIMS). The Zr/Hf ratios of all investigated samples from the Balmuccia peridotite complex are significantly lower than the chondritic value of 34.2, and the most depleted samples have Zr/Hf ratios as low as 10. Correlated Zr/Hf ratios and Zr abundances of the lherzolites preserve the trend of a mantle residue that has been depleted by fractional melting. This trend confirms experimental studies that predict Hf to behave more compatibly than Zr during mantle melting. Experimentally determined partition coefficients imply that the major Zr and Hf depletion most likely occurred in the spinel stability field, with (D_Zr/D_Hf)^cpx≈0.5, and not in the garnet stability field, where (D_Zr/D_Hf)^grt is probably close to one. However, minor amounts of melting must have also occurred in a garnet facies mantle, as indicated by low Sm/Lu ratios in the Balmuccia peridotites. The Nb/Ta ratios of most lherzolites are subchondritic and vary only from 7 to 10, with the exception of three samples that have higher Nb/Ta ratios (18–24). The overall low Nb/Ta ratios of most depleted mantle rocks confirm a higher compatibility of Ta in the mantle. The uniform Nb/Ta ratios in most samples imply that even in ‘depleted’ mantle domains the budget of the highly incompatible Nb and Ta is controlled by enrichment processes. Such a model is supported by the positive correlation of Zr/Nb with the Zr concentration. However, the overall enrichment was weak and did barely affect the moderately incompatible elements Zr and Hf. The new constraints from the partitioning behaviour of Zr–Hf and Nb–Ta provide important insights into processes that formed the Earth’s major silicate reservoirs. The correlation of Zr/Hf and Sm/Nd in depleted MORB can be assigned to previous melting events in the MORB source. However, such trends were unlikely produced during continental crust formation processes, where Sm/Nd and Zr/Hf are decoupled. The different fractionation behaviour of Zr/Hf and Sm/Nd in the depleted mantle (correlated) and the crust (decoupled) indicates that crustal growth by a simple partial melting process in the mantle has little effect on the mass budget of LREE and HFSE between crust and mantle. A more complex source composition, similar to that of modern subduction rocks, is needed to fractionate the LREE, but not Zr/Hf and the HREE.     

Mineral chemistry,P-T-t paths and exhumation processes of mafic granulites in Dinggye,Southern Tibet

Lower crustal high grade metamorphic rocks have been successively found at Pamirs nearby the western Himalayan syntaxis, Namjagbarwa and Dinggye nearby the eastern Himalayan syntaxis and the central segment of the Himalayan Orogenic Belt, respec-tively[1―4]. In particular, some researchers deduced that there were probably eclogites at some locations[5]. Moreover, some geochronological data of these lower crustal granulites also have been accumulated. For example, the high-pressure granulit…     

High-pressure phase equilibria in a garnet lherzolite,with special reference to Mg2+Fe2+ partitioning among constituent minerals

Phase equilibria in a natural garnet lherzolite nodule (PHN 1611) from Lesotho kimberlite and its chemical analogue have been studied in the pressure range 45–205 kbar and in the temperature range 1050–1200°C. Partition of elements, particularly Mg²⁺Fe²⁺, among coexisting minerals at varying pressures has also been examined. High-pressure transformations of olivine(α) to spinel(γ) through modified spinel(β) were confirmed in the garnet lherzolite. The transformation behavior is quite consistent with the information previously accumulated for the simple system Mg₂SiO₄Fe₂SiO₄. At pressures of 50–150 kbar, a continuous increase in the solid solubility of the pyroxene component in garnet was demonstrated in the lherzolite system by means of microprobe analyses. At 45–75 kbar and 1200°C, the Fe²⁺/(Mg + Fe²⁺) value becomes greater in the ascending order orthopyroxene, Ca-rich clinopyroxene, olivine and garnet. At 144–146 kbar and 1200°C, garnet exhibits the highest Fe²⁺/(Mg + Fe²⁺) value; modified spinel(β) and Ca-poor clinopyroxene follow it. When the modified spinel(β)-spinel(γ) transformation occurred, a higher concentration of Fe²⁺ was found in spinel(γ) rather than in garnet. As a result of the change in the Mg²⁺Fe²⁺ partition relation among coexisting minerals, an increase of about 1% in the Fe₂SiO₄ component in (Mg,Fe)₂SiO₄ modified spinel and spinel was observed compared with olivine.These experimental results strongly suggest that the olivine(α)-modified spinel(β) transformation is responsible for the seismic discontinuity at depths of 380–410 km in the mantle. They also support the idea that the minor seismic discontinuity around 520 km is due to the superposition effect of two types of phase transformation, i.e. the modified spinel(β)-spinel(γ) transformation and the pyroxene-garnet transformation. Mineral assemblages in the upper mantle and the upper half of the transition zone are given as a function of depth for the following regions: 100–150, 150–380, 380–410, 410–500, 500–600 and 600–650 km.     

Petrology of the Yugu peridotites in the Gyeonggi Massif,South Korea: Implications for its origin and hydration process

Peridotites exposed in the Yugu area in the Gyeonggi Massif, South Korea, near the boundary with the Okcheon Belt, exhibit mylonitic to strongly porphyroclastic textures, and are mostly spinel lherzolites. Subordinate dunites, harzburgites, and websterites are associated with the lherzolites. Amphiboles, often zoned from hornblende in the core to tremolite in the rim, are found only as neoblasts. Porphyroclasts have recorded equilibrium temperatures of about 1000°C, whereas neoblasts denote lower temperatures, about 800°C. Olivines are Fo_90–91 in lherzolites and Fo₉₁ in a dunite and a harzburgite. The Cr# (= Cr/(Cr + Al) atomic ratio) of spinels varies together with the Fo of olivines, being from 0.1 to 0.3 in lherzolites and around 0.5 in the dunite and harzburgite. The Na₂O content of clinopyroxene porphyroclasts is relatively low, around 0.3 to 0.5 wt% in the most fertile lherzolite. The Yugu peridotites are similar in porphyroclast mineral chemistry not to continental spinel peridotites but to sub‐arc or abyssal peridotites. Textural and mineralogical characteristics indicate the successive cooling with hydration from the upper mantle to crustal conditions for the Yugu peridotites. Almost all clinopyroxenes and amphiboles show the same U‐shaped rare earth element (REE) patterns although the level is up to ten times higher for the latter. The hydration was associated with enrichment in light REE, resulting from either a slab‐derived fluid or a fluid circulating in the crust. The mantle‐wedge or abyssal peridotites were emplaced into the continental crust as the Yugu peridotite body during collision of continents to form a high‐pressure metamorphic belt in the Gyeonggi Massif. The peridotites from the Gyeonggi Massif exhibit lower‐pressure equilibration than peridotites, with or without garnets, from the Dabie–Sulu Collision Belt, China, which is possibly a westward extension of the Gyeonggi Massif.     

由包体推导的河北汉诺坝下地壳-上地幔地温线及其地质意义

通过对采自河北汉诺坝玄武岩中的下地壳和上地幔包体的详细研究 ,建立了本区下地壳—上地幔地温线。该地温线高于大洋地温线和古老地盾地温线 ,接近克拉通边缘的地温线 ,符合该区的大地构造环境。由该地温线建立的下地壳—上地幔地质结构剖面表明 ,该区下地壳主要由不同类型的麻粒岩相岩石组成 ,其化学成分以镁铁质为主 ,深度范围为 2 5～ 4 2km。上地幔由超镁铁质的二辉橄榄岩组成 ,在尖晶石二辉橄榄岩和石榴石二辉橄榄岩之间有一过渡层。由地温线确定的壳幔边界位于 4 2km附近 ,与地震资料确定的莫霍面一致 ,但在壳幔边界之上的下地壳底部有下地壳麻粒岩和超镁铁质岩的互层。这一现象可以解释在下地壳底部常见的层状反射层。该区岩石圈底界大约在 95km ,其下的软流层仍由石榴石二辉橄榄岩组成     

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.     

Indosinian anatexis of Paleoproterozoic granites in the east Cathaysia Block,South China

Granulite facies metamorphism and crustal anatexis exist in the East Cathaysia Block, the exact timing of granulite facies partial melting and its link with orogenesis have not been well constrained. In this study, we carried out petrography, whole rock geochemistry, and zircon U–Pb dating, trace elements and Hf isotopes analyses on Dazhe gneissic granite and banded migmatite from the Badu Group in southwest Zhejiang province in the East Cathaysia Block. The melts were produced through the dehydration of biotite, such as biotite + quartz + plagioclase = orthopyroxene + K-feldspar + melt and biotite + quartz + plagioclase + sillimanite = garnet + K-feldspar + melt. Zircons from these rocks show clear core-rim structure and yield rim and core concordant ages at 233 Ma and 1.83 Ga, respectively. The zircon rims suggesting the melts and the cores are suggesting the protolith of Dazhe gneissic granite and banded migmatite were crystallized from an evolving magma. The zircon cores and rims have negative ε_Hf(t) = −2.2 ~ −6.3 and ε_Hf(t) = −22.8 ~ −32.4, and they give suggestion of the presence of Neoarchean components. Although the major-element compositions of the gneissic granite and banded migmatite are slightly different, the trace-element spider diagram and REE pattern show they are similar, and then we find that the protoliths are A-type granodiorite/diorite. Combined with the published data, we suggested that the Dazhe gneissic granite and banded migmatite were formed through granulite facies partial melting at 233 Ma, which was promoted by crustal shortening and thickening of the collision orogeny between East Cathaysia Block and an unknown terrane with a NNE trend structure line. The protoliths (granite or granodiorite) of Dazhe gneissic granite and banded migmatite crystallized at 1.83 Ga by reworking of the Neoarchean components of East Cathaysia Block. The Paleoproterozoic (1912–1819 Ma) collisional orogeny and the later intraplate rifting stage are corresponding to the aggregation and breakup of the Columbia supercontinent.     

Chromian spinel lamellae in olivine from the Iwanai-dake peridotite mass,Hokkaido, Japan

Lamellar inclusions of chromian spinel (Cr/Cr + Al> 0.7), clinopyroxene and chromian spinel-clinopyroxene symplectite occur in olivines from alpine-type peridotites which have equilibrated at relatively low temperature (<700°C). They occur most commonly in dunite with very magnesian olivine (Fo₉₃ to Fo₉₅) and discrete grains of Cr-rich spinel. Olivine which initially equilibrated with magnesian and Cr-rich liquid had contained small amounts of calcium and trivalent chromium in the octahedral site, and lamellar chromian spinel and diopsidic clinopyroxene exsolved during the annealing process. The ordinary depletion of chromium or absence of chromian spinel lamellae in olivines in igneous rocks may be partly due to the effective exclusion of chromium from olivine upon cooling.