Origin of Neoproterozoic ophiolitic peridotites in south Eastern Desert, Egypt, constrained from primary mantle mineral chemistry

The ophiolitic peridotites in the Wadi Arais area, south Eastern Desert of Egypt, represent a part of Neoproterozoic ophiolites of the Arabian-Nubian Shield (ANS). We found relics of fresh dunites enveloped by serpentinites that show abundances of bastite after orthopyroxene, reflecting harzburgite protoliths. The bulk-rock chemistry confirmed the harzburgites as the main protoliths. The primary mantle minerals such as orthopyroxene, olivine and chromian spinel in Arais serpentinites are still preserved. The orthopyroxene has high Mg# [=Mg/(Mg + Fe²⁺)], ~0.923 on average. It shows intra-grain chemical homogeneity and contains, on average, 2.28 wt.% A1₂O₃, 0.88 wt.% Cr₂O₃ and 0.53 wt.% CaO, similar to primary orthopyroxenes in modern forearc peridotites. The olivine in harzburgites has lower Fo (93?94.5) than that in dunites (Fo_94.3?Fo_95.9). The Arais olivine is similar in NiO (0.47 wt.% on average) and MnO (0.08 wt.% on average) contents to the mantle olivine in primary peridotites. This olivine is high in Fo content, similar to Mg-rich olivines in ANS ophiolitic harzburgites, because of its residual origin. The chromian spinel, found in harzburgites, shows wide ranges of Cr#s [=Cr/(Cr + Al)], 0.46?0.81 and Mg#s, 0.34?0.67. The chromian spinel in dunites shows an intra-grain chemical homogeneity with high Cr#s (0.82?0.86). The chromian spinels in Arais peridotites are low in TiO₂, 0.05 wt.% and Y_Fe [= Fe³⁺/(Cr + Al + Fe³⁺)], ~0.06 on average. They are similar in chemistry to spinels in forearc peridotites. Their compositions associated with olivine’s Fo suggest that the harzburgites are refractory residues after high-degree partial melting (mainly ~25?30 % partial melting) and dunites are more depleted, similar to highly refractory peridotites recovered from forearcs. This is in accordance with the partial melting (>20 % melt) obtained by the whole-rock Al₂O₃ composition. The Arais peridotites have been possibly formed in a sub-arc setting (mantle wedge), where high degrees of partial melting were available during subduction and closing of the Mozambique Ocean, and emplaced in a forearc basin. Their equilibrium temperature based on olivine?spinel thermometry ranges from 650 to 780 °C, and their oxygen fugacity is high (Δlog ?O₂?=?2.3 to 2.8), which is characteristic of mantle-wedge peridotites. The Arais peridotites are affected by secondary processes forming microinclusions inside the dunitic olivine, abundances of carbonates and talc flakes in serpentinites. These microinclusions have been formed by reaction between trapped fluids and host olivine in a closed system. Lizardite and chrysotile, based on Raman analyses, are the main serpentine minerals with lesser antigorite, indicating that serpentines were possibly formed under retrograde metamorphism during exhumation and near the surface at low T (<400 °C).     

Petrology and geochemistry of Abyssal Peridotites from the Manipur Ophiolite Complex,Indo-Myanmar Orogenic Belt,Northeast India: Implication for melt generation in mid-oceanic ridge environment

The Manipur Ophiolite Complex (MOC) located in the Indo-Myanmar Orogenic Belt (IMOB) of Northeast India forms a section of the Tethyan Ophiolite Belt of the Alpine–Himalayan orogenic system. Whole rock compositions and mineral chemistry of mantle peridotites from the MOC show an affinity to the abyssal peridotites, characterized by high contents of Al₂O₃ (1.28–3.30 anhydrous wt.%); low Cr# of Cr-spinel (0.11–0.27); low Mg# of olivine (∼Fo₉₀) and high Al₂O₃ in pyroxenes (3.71–6.35 wt.%). They have very low REE concentrations (∑REE = 0.48–2.14 ppb). Lherzolites display LREE-depleted patterns (La_N/Sm_N = 0.14–0.45) with a flat to slightly fractionated HREE segments (Sm_N/Yb_N = 0.30–0.65) whereas Cpx-harburgites have flat to upward-inflected LREE patterns (La_N/Sm_N = 0.13–1.23) with more fractionated HREE patterns (Sm_N/Yb_N = 0.13–0.65) than the lherzolite samples. Their platinum group elements (PGE) contents (<50 ppb) and distinct mantle-normalised PGE patterns with the Pd/Ir values (1.8–11.9) and Pt/Pt^* values (0.2–1.1) show an affinity to the characteristic of the residual mantle material. Evaluation of mineralogical and petrological characteristics of these peridotites suggests that they represent the residues remaining after low degree of partial melting (∼2–12%) in the spinel stability field of a mid-oceanic ridge environment. The well-preserved mid-oceanic ridge characteristics of these peridotites further suggest that the mantle section was subsequently trapped in the forearc region of the subduction zone without undergoing significant modification in their chemistry by later subduction-related tectonic and petrological processes before its emplacement to the present crustal level.     

Mesoproterozoic olivine gabbronorites of the Bashkirian anticlinorium,the South Urals: Parental melts and specifics of magma evolution

This paper is devoted to detailed study of picritic rocks (olivine melanogabbronorites) and comagmatic gabbrodolerites from sills and dikes in the central part of the Bashkirian meganticlinorium. These rocks are ascribed to the Kama-Belsk magmatic province (KBP) that was formed in the eastern East European Platform (EEP) in the Mesoproterozoic time. The study of minerals (EMPA, SIMS), rocks, and their oxygen isotope compositions showed the contribution of crustal contamination, fractional crystallization and cumulus processes in their formation. The geochemical indicators of crustal contamination (Nb/Nb*, (Nb/La) _n , δ¹⁸O, and others) show strong variations, which indicates uneven crustal contribution in the parental melts during rock formation (10–25%). The study of weakly contaminated (δ¹⁸O = 5.3‰) olivine melanogabbronorites (MgO = 22.55 wt %) from the small Ishlya-1 subvolcanic body, which contain subordinate amount of cumulus (24%), high-magnesian olivine (Fo91.3), and high-Cr spinel (cr# 0.67), as well as HREE depleted clinopyroxenes, allowed us to retrieve the composition of parental melt. The latter contained about 20 wt % MgO and was formed by 19–26% melting of mantle source (potential mantle temperature T _m of 1530–1545°C). Geochemical characteristics of KBP reflect the formation of primary melts by melting of mantle column at different depths, mixing of the melts, and significant contamination by crustal material. The dominant role in the formation of the rocks of the Ishlya area and Mashak Complex was played by derivatives of spinel peridotites, while the rocks of the Bakal-Satka area were derived from garnet peridotites.     

Geochemistry of mid-ocean ridge mafic intrusives from the Manipur Ophiolitic Complex,Indo-Myanmar Orogenic Belt,NE India

Mafic intrusives emplaced within the mélange zone of the Manipur Ophiolitic Complex are subalkalinetholeiitic affinity with Fe-enrichment. Based on the field occurrences, textures-mineralogy and whole-rock compositions, these mafic intrusives can be identified as type-I (gabbro intrusives) and type-II (basalt-dolerite dykes). The type-I resembling enriched-type mid-ocean ridge basalt (E-MORB) shows moderate LREE enrichment (La_N/Sm_N = 2.5–2.6), slightly enriched MORB normalized HFSE patterns possibly represent melts derived from enriched MORB sub-oceanic mantle sources by small degree of partial melting. The other type-II has normal-type mid-ocean ridge basalt (N-MORB) geochemical features, as it exhibits nearly flat to depleted LREE (La_N/Sm_N = 1.0–0.6), flat MORB normalized HFSE patterns with slight LREE/HREE depletion (Ce_N/Yb_N = 1.37–0.46). It might have been derived from depleted MORB type sub-oceanic mantle source. The MORB signature displayed by these mafic intrusives indicates that they are dismembered fragments of oceanic crust generated at mid-ocean spreading ridge system and support the hypothesis that the Manipur ophiolites was initially formed in the divergent plate margin.     

Mesoproterozoic orangeites (Kimberlites II) of West Karelia: Mineralogy,geochemistry, and Sr-Nd isotope composition

Mineralogical and petrological-geochemical features of the Mesoproterozoic (1.23–1.20 Ga) alkaline ultrabasic rocks from the Kostomuksha-Taloveis (Russia) and Lentiira-Kuhmo (Finland) areas, West Karelia, have been studied. In terms of mineralogy and geochemistry, these rocks more resemble group II kimberlites of South Africa (orangeites) than olivine lamproites or ultramafic lamprophyres. On the basis of phenocryst composition, the studied orangeites are divided into three types: Cpx-Phl-Ol, Phl-Ol, and Phl-Carb orangeites. The Cpx-Phl-Ol orangeites from the Kostomuksha cluster clearly differ from analogous rocks from the Lentiira cluster. The composition of Phl-Ol orangeites is indicative of derivation by intense fractional crystallization; Cpx-Phl-Ol orangeites from the Kostomuksha area display evidence of intense lithosphere assimilation. The Phl-Carb orangeites from the Taloveis cluster and Cpx-Ol orangeites from the Lentiira cluster most closely approximate primary melts. The Kostomuksha orangeites are characterized by lowto moderate-radiogenic (⁸⁷Sr/⁸⁶Sr)1220 ratio varying from 0.7038 to 0.7067. The Phl-Carb orangeites of Taloveis have less radiogenic Nd isotope composition (?_Nd from ?11 to ?12) as compared to the Cpx-Phl-Ol and Phl-Ol orangeites of Kostomuksha (?_Nd from ?6.9 to ?9.4). The Cpx-Phl-Ol orangeites from Lentiira contain fresh olivine. By morphology and composition, there are three olivine generations: (1) large rounded, usually zoned crystals with Fo ₉₂ core, 0.33–0.37 wt % NiO, and 0.03–0.04 wt% CaO, which are interpreted as xenocrysts from depleted peridotites; (2) anhedral rounded zoned olivines of intermediate size with Fo _82–83 cores, 0.03–0.05 wt % CaO, 0.12–0.17 wt % NiO, and up to 0.40 wt % MnO. These olivines were entrapped by orangeite melt and presumably represent a cumulate of basaltic melts or were derived from metasomatized peridotites; (3) fine euhedral olivines and xenocryst rims corresponding to Fo _88–89 with 0.10–0.42 wt % CaO, 0.14–0.35 wt % NiO, and up to 0.07–0.21 wt % MnO; their origin was presumably related to the crystallization from kimberlite melt. The calculation of $f_{O_2 }$ of kimberlite melt during crystallization of perovskites using Nb-Fe perovskite oxyba-rometer showed that Cpx-Phl-Ol orangeites of Kostomuksha and orangeites of Lentiira crystallized at similar oxygen fugacities corresponding to ΔNNO from ?3.3 to ?1.1 and from ?3.3 to ?0.9, respectively. The Sm-Nd and Rb-Sr isotope study provided evidence for the contribution from ancient enriched source in the genesis of the orangeites. It was proposed that their mantle source was formed in two stages: (1) metasomatic reworking of previously depleted lithospheric source at the Karelian Craton base during Paleoproterozoic orogenic events 2.1–2.0 Ga ago; (2) extension-related generation of orangeite melts 1.27–1.20 Ga ago.     

Composition and evolution of the lithospheric mantle beneath the interior of the South China Block: insights from trace elements and water contents of peridotite xenoliths

Major and trace elements and water contents were analyzed in 16 peridotite xenoliths embedded by the Cenozoic basalts in Pingnan (southeastern Guangxi Province), to constrain the chemical composition and evolution of the lithospheric mantle located in the central part of the South China Block (SCB). The peridotites are mainly moderately refractory harzburgites and lherzolites (Mg#-Ol?=?90.3–91.7) and minor fertile lherzolites (Mg#-Ol?=?88.9–89.9). Clinopyroxenes in the peridotites show LREE-depleted pattern, and commonly exhibit negative anomalies in Nb and Ti, suggesting the peridotites probably represent residues after 1–10% of partial melting without significant mantle metasomatism. Water contents range from 146 to 237 ppm wt. H₂O in clinopyroxene, and from 65 to 112 ppm wt. H₂O, in orthopyroxene but are below detection limit (2 ppm wt. H₂O) in olivine. Calculated bulk water contents, based on the mineral modes and partition coefficient, range from 14 to 83 ppm wt. H₂O (average 59 ppm wt. H₂O). There is a correlation between melting indices (such as Mg#-Ol, Yb_n in clinopyroxene) and water contents in clinopyroxene and orthopyroxene, but no correlation is observed between the whole-rock water contents and the redox state (Fe³⁺/∑Fe ratios in spinel), suggesting that water contents in the peridotites are mainly controlled by the degree of partial melting rather than by oxygen fugacity. The lithospheric mantle beneath the interior of the SCB may not be compositionally stratified; fertile and moderately refractory mantle coexist at the similar depths. Geochemical data and water contents of the studied peridotites are similar to the proposed MORB source and indicate that the ancient refractory lithospheric mantle was irregularly eroded or reacted by the upwelling asthenosphere, and eventually replaced by juvenile fertile accreted mantle through the cooling of the asthenosphere.     

Using platinum-group elements and Au geochemistry to constrain the genesis of podiform chromitites and associated peridotites from the Soghan mafic–ultramafic complex,Kerman, Southeastern Iran

The podiform chromite deposit of the Soghan mafic–ultramafic complex is one of the largest chromite deposits in south-east Iran (Esfandagheh area). The Soghan complex is composed mainly of dunite, harzburgite, lherzolite, pyroxenite, chromitite, wehrlite and gabbro. Olivine, orthopyroxene, and to a lesser extent clinopyroxene with highly refractory nature, are the primary silicates found in the harzburgites and dunites. The forsterite content of olivine is slightly higher in dunites (Fo₉₄) than those in harzburgites (Fo₉₂) and lherzolites (Fo₈₉). Chromian spinel mainly occurs as massive chromitite pods and as thin massive chromitite bands together with minor disseminations in dunites and harzburgites. Chromian spinels in massive chromitites show very high Cr-numbers (80–83.6), Mg-numbers (62–69) and very low TiO₂ content (averaging 0.17 wt.%) for which may reflect the crystallization of chromite from a boninitic magma. The Fe^3 +-number is very low, down to < 0.04 wt.%, in the chromian spinel of chromitites and associated peridotites of the Soghan complex.PGE contents are variable and range from 80 to 153 pbb. Chromitites have strongly fractionated chondrite-normalized PGE patterns, which are characterized by enrichments in Os, Ir and Rh relative to Pt and Pd. Moreover, the Pd/Ir value which is an indicator of PGE fractionation ranges from < 0.08 to 0.24 in chromitite of the Soghan complex. These patterns and the low PGE abundances are typical of ophiolitic chromitites and indicating a high degree of partial melting (about 20–24%) of the mantle source. Moreover, the Pd_N/Ir_N ratios in dunites are unfractionated, averaging 1.2, whereas the harzburgites and lherzolites show slightly positive slopes PGE spidergrams, together with a small positive Ru and Pd anomaly, and their Pd_N/Ir_N ratio averages 1.98 and 2.15 respectively.The mineral chemistry data and PGE geochemistry, along with the calculated parental melts in equilibrium with chromian spinel of the Soghan chromitites indicate that the Soghan complex was generated from an arc-related magma with boninitic affinity above a supra-subduction zone setting.     

Investigation on mantle peridotites from Neyriz ophiolite, south of Iran: geodynamic signals

Neyriz ophiolite in Abadeh Tashk area appears as four major separated massifs in an area with 125 km², south of Iran. Peridotites including harzburgite, dunite, and lesser low-Cpx lherzolite are the major constituents of the ophiolite with very minor mafic rocks. Usual gabbros of ophiolite complexes are virtually absent from the study area. Mineral modality associated with bulk rock and mineral chemistry of the peridotites show a progression from fertile to ultra-refractory character, reflected by a progressive decrease in modal pyroxenes and in Al₂O₃, CaO, SiO₂, Sc, Ta, V, and Ga values of the studied rocks by approaching chromite deposits. The Neyriz peridotites vary from low-Cpx lherzolite (MgO, 41.97–43.1 wt.%; Al₂O₃, 0.8–1.3 wt.%) with low content of Cr# spinel (36.7–37.6) and Fo olivine (90.79–91.5) to harzburgite (MgO, 44.31–45.25 wt.%;Al₂O₃, 0.29–0.45 wt.%; Cr# spinel, 58.2–73.45; Fo olivine, 91.23–91.56), and then to dunite (MgO, 45.9–49.2 wt.%; Al₂O₃, 0.18–0.48 wt.%) with higher content of Cr# spinel (74.34–79.36) and Fo olivine (91.75–94.68). Compared to modern oceanic settings, mineral and rock composition of low-Cpx lherzolite plot within the field of mid-ocean-ridge environment, whereas those of harzburgite and dunite fall in the field of fore-arc peridotites. As a result of the studies on minerals and whole rock chemistry along with rock interrelationships, we contend that the peridotites were subsequently affected by percolating hydrous boninitic melt from which the high-Cr–Mg, low-Ti chromitites were formed within mantle wedge above the supra-subduction zone in a fore-arc setting.     

Hydrous peridotites with Ti-rich chromian spinel as a low-temperature forearc mantle facies: evidence from the Happo-O’ne metaperidotites (Japan)

The Happo-O’ne peridotite complex is situated in the northeastern part of the Hida Marginal Tectonic Zone, central Japan, characterized by the high-P/T Renge metamorphism, and is considered as a serpentinite mélange of Paleozoic age. Peridotitic rocks, being massive or foliated, have been subjected to hydration and metamorphism. Their protoliths are mostly lherzolites to harzburgites with subordinate dunites. We found a characteristic mineral assemblage, olivine + orthopyroxene + tremolite + chlorite + chromian spinel, being stable at low-T, from 650 to 750°C, and high-P, from 16 to 20 kbar, tremolite–chlorite peridotites of the tremolite zone. Olivines are Fo₈₈–Fo_91, and orthopyroxenes (Mg# = 0.91) show low and homogenous distributions of Al₂O₃ (up to 0.25 wt%), Cr₂O₃ (up to 0.25 wt%), CaO (up to 0.36 wt%) and TiO₂ (up to 0.06 wt%) due to the low equilibration temperature. Chromian spinels, which are euhedral and enclosed mainly in the orthopyroxenes, have high TiO_2, 3.1 wt% (up to 5.7 wt%) on average, and high Cr# [=Cr/(Cr + Al) atomic ratio], 0.95 on average but low Fe³⁺ [=Fe³⁺/(Cr + Al + Fe³⁺) atomic ratio, <0.3]. The bulk-rock chemistry shows that the Happo-O’ne metaperidotites with this peculiar spinel are low in TiO₂ (0.01–0.02 wt%), indicating no addition of TiO₂ from the outside source during the metamorphism; the high TiO₂ of the peculiar spinel has been accomplished by Ti release from Ti-bearing high-T pyroxenes during the formation of low-T, low-Ti silicates (<0.1 wt% TiO₂) during cooling. Some dunites are intact from hydration: their olivine is Fo₉₂ and spinel shows high Cr#, 0.72. The Happo-O’ne metaperidotites (tremolite–chlorite peridotites), being in the corner of the mantle wedge, are representative of a hydrous low-T, high-P mantle peridotite facies transitional from a higher T anhydrous peridotite facies (spinel peridotites) formed by in situ retrograde metamorphism influenced by fluids from the subducting slab. They have suffered from low-T (<600°C) retrogressive metamorphism to form antigorite and diopside during exhumation of the Renge metamorphic belt.     

Na,K, P and Ti in garnet,pyroxene and olivine from peridotite and eclogite xenoliths from African kimberlites

Electron microprobe analyses sensitive to 20ppmw (2σ) were made for Na, P, K and Ti in garnet, pyroxenes and olivine from peridotite and eclogite xenoliths from African kimberlites and volcanic rocks in Tanzania. Average concentrations (ppmw) in peridotite (mostly garnet lherzolite) are: Na₂O gt 340 ol 90 opx 1070 cpx 2.1 (wt.%); P₂O₅ gt 460 ol 130 opx 50 cpx 350; K₂O gt <20 ol <20 opx 30 cpx 170; TiO₂ gt 1470 ol 130 opx 480 cpx 1630. For eclogites and a cpx megacryst with gt inclusions: Na₂O gt 610 cpx 4.3 (wt.%); P₂O₅ gt 530 cpx 300; K₂O gt <20 cpx 370; TiO₂ gt 1990 cpx 1980.In garnet, Na can be explained by coupled substitution with P and Ti, and there is no need to invoke six-coordinated silicon. The Na distribution between garnet and clinopyroxene correlates with the Fe/Mg distribution for both eclogites and peridotites, and for the peridotites correlates with estimates of pressure and temperature from pyroxene composition. When calibrated experimentally, the Na distribution may be a useful indicator of physical conditions at depths for which the Fe/Mg distribution is insensitive; furthermore the Na distribution may be less sensitive to oxidation state.     

An early Palaeozoic supra-subduction lithosphere in the Variscides: new evidence from the Maures massif

Petrographic and geochemical studies of peridotites and melagabbros from the Maures massif (SE France) provide new constraints on the Early Palaeozoic evolution of the continental lithosphere in Western Europe. Peridotites occur as lenses along a unit rooted in the main Variscan suture zone. They are dominantly spinel peridotites and minor garnet–spinel peridotites. Spinel peridotites represent both residual mantle and ultramafic cumulates. Mantle-related dunites and harzburgites display high temperature textures, with olivine (Mg#_0.90), orthopyroxene (Mg#_0.90) and spinel (TiO₂ < 0.2%; Cr#_0.64–0.83) compositions typical of fore-arc upper mantle. Ultramafic cumulates are dunite adcumulates, harzburgite heteradcumulates and mesocumulates, melagabbro heteradcumulates and amphibole peridotites, with olivine (Mg#_0.85–0.89), orthopyroxene (Mg#_0.86–0.89) and Cr-spinel (TiO₂ = 0.5–3.3%; Cr#_0.7–0.98) compositions typical of ultramafic cumulates. Cr-spinel compositions of both spinel peridotite types suggest their genesis in a supra-subduction zone lithosphere. Core to rim zoning in spinel is related to the incomplete influence of regional metamorphism and serpentinisation. The covariation of major and minor elements with Al₂O₃ for cumulates is consistent with igneous processes involving crystal accumulation. Both mantle and cumulate dunites and harzburgites have U-shaped REE patterns and extremely low trace element contents, similar to peridotites from modern fore-arc peridotites (South Atlantic) and from ophiolites related to supra-subduction zones (Semail, Cyclops, Pindos, Troodos). Melagabbros also have U-shaped REE patterns similar to xenoliths from the Philippine island arc, but also similar to intrusive ultramafic cumulates from the Semail nappe of Oman related to a proto-subduction setting. A wehrlite has a REE pattern similar to that of amphibole peridotites reflecting metasomatism of clinopyroxene-bearing peridotites due to subduction-related fluids. The Maures spinel peridotites and melagabbros are therefore interpreted as the lowermost parts of a crustal sequence and minor residual mantle of lithosphere generated in a supra-subduction zone during Early Palaeozoic time. Garnet–spinel peridotites are chemically close to melagabbros, but have recorded high pressure metamorphism before their retrogression similar to spinel peridotites into amphibolites to greenschists facies metamorphism. They indicate burial to mantle depths of the margin of the supra-subduction lithosphere during the Early Palaeozoic continental subduction. Both peridotite types were exhumed during the Upper Palaeozoic continental collision. Comparable observations from other Variscan-related peridotites, in particular of the Speik complex of the Autroalpine basement, and a common age for the subduction stage allow extension of these regional conclusions to a broad area sharing the Cambrian suture zone, extending from the Ossa-Morena to the Bohemian massif.     

Compositional signatures of SSZ-type peridotites from the northern Vourinos ultra-depleted upper mantle suite,NW Greece

The northern Vourinos massif, located in the Dinarides-Hellenides mountain belt in the Balkan Peninsula, forms a section of the so-called Neotethyan ophiolitic belt in the Alpine-Himalayan orogenic system. It is comprised mainly of a well-preserved mantle sequence, dominated by voluminous massive harzburgite with variable clinopyroxene and olivine modal abundances, accompanied by subordinate coarse- and fine-grained dunite. The harzburgite rock varieties are characterized by high Cr# [Cr/(Cr + Al)] values in Cr-spinel (0.47–0.74), elevated Mg# [Mg/(Mg + Fe²⁺)] in olivine (0.90–0.93), low Al₂O₃ content in clinopyroxene (≤1.82 wt.%) and low average bulk-rock concentrations of CaO (0.52 wt.%) and Al₂O₃ (0.40 wt.%), which are indicative of their refractory nature. In addition, dunite-type rocks display even more depleted compositions, containing Cr-spinel and olivine with higher Cr# (0.76–0.84) and Mg# (0.91–0.94), respectively. They also display extremely low average abundances of CaO (0.13 wt.%) and Al₂O₃ (0.15 wt.%). The vast majority of the studied peridotites are also strongly depleted in REE. Simple batch and fractional melting models are not sufficient to explain their ultra-depleted composition. Whole-rock trace element abundances of the northern Vourinos mantle rocks can be modeled by up to 22–31% closed-system non-modal dynamic melting of an assumed primitive mantle (PM) source having spinel lherzolite composition. The highly depleted compositional signatures of the investigated peridotites indicate that they have experienced hydrous melting in the fore-arc mantle region above a SSZ. This intense melting event was responsible for the release of arc-related melts from the mantle. These melts reacted with the studied peridotites causing incongruent melting of pyroxenes followed by considerable olivine and Cr-spinel addition in terms of cryptic metasomatism. This later metasomatic episode has obscured any geochemical fingerprints indicative of an early mantle melting event in a MOR setting. The lack of any MOR-type peridotites in the northern Vourinos depleted mantle suite is quite uncommon for SSZ-type Neotethyan ophiolites.     

Petrology of ultramafic xenoliths from Kishyuku Lava,Fukue-jima,Southwest Japan

 Ultramafic xenoliths are found in Kishyuku Lava, Fukue-jima, Southwest Japan. These include spinel lherzolite, harzburgite and dunite, as well as pyroxenite. The compositions of the constituent minerals of the peridotite xenoliths are in the range of upper mantle peridotites. Variable Cr/(Cr+Al) ratios (0.1–0.5) of spinel, together with a limited range in olivine composition (Fo₉₀–Fo₉₂), indicate that the xenoliths are derived from slightly to highly depleted residual mantle. The combination of previously published clinopyroxene-olivine geothermobarometry and clinopyroxene-orthopyroxene geothermometry applied to the xenoliths yields a high geotherm of 1070° C at 1.0 GPa up to 1200° C at 2.2 GPa. Existence of such depleted upper mantle is compatible with the existing model of asthenospheric injection during the rifting of the Northeast China and the Japan Sea. The high geotherm is caused by thermal perturbation due to the injection of the hot asthenosphere and/or post-rifting uprise of mantle diapirs since 11 Ma. Received: 15 May 1995 / Accepted: 3 January 1996     

Origin and evolution of Suru Valley ophiolite peridotite slice along Indus suture zone,Ladakh Himalaya,India: Implications on melt-rock interaction in a subduction-zone environment

In this paper, we present whole-rock and mineral geochemistry of serpentinized peridotites from the Suru Valley ophiolite slice Ladakh Himalaya, in an attempt to put constraints on their petrogenesis and tectonic evolution in the context of Mesozoic Neo-Tethys Ocean. On the basis of petrographic study, Suru Valley serpentinized peridotites can be identified as serpentinized harzburgites. Relative to primitive mantle these rocks have depleted major and rare earth element (REE) geochemical characteristics comparable to ocean floor mantle rocks reflecting their mantle residual nature. However, higher abundance of highly incompatible large ion lithophile elements (e.g., Rb, Ba, Th, U, Pb and Sr), reflect metasomatism in a subduction zone environment. The presence of silicate assemblage includes Mg-rich olivine (Fo_90-92) and orthopyroxene (En_91-93 Fs_6.4-8.7) of supra-subduction zone affinity. Evaluation of mineral and whole-rock geochemistry suggests that the Suru Valley ophiolitic peridotites represent residues left after moderate degrees of partial melting thereby underwent metasomatism in a supra-subduction zone environment related to north dipping intra-oceanic island arc during Cretaceous in the context of Mesozoic Neo-Tethys ocean.     

Occurrence of népouite in the serpentinite of the Manipur ophiolite belt,Northeastern India: Implication for melt-rock interaction in a supra-subduction zone

Serpentinization is pervasive in the ultramafic rocks of Manipur ophiolite belt (MOB), Northeastern India. Electron microprobe data of a serpentinite from the Ukhrul-Nungbi sector of MOB shows Ni-rich serpentine mineral (NiO = 33.4-33.9 wt %, SiO₂= 37.55-38.96 wt %, MgO= 14.83-16.89 wt %). The composition and X-ray diffraction pattern characterize this Ni-rich serpentine mineral as népouite which is suggested to be a hydrothermal alteration product of NiO-rich olivine in a fore-arc peridotite. The genesis of this NiO-rich olivine is attributed to the melt-rock interaction in a supra-subduction zone setting.     

Boninite primary magmas: Evidence from the Cape Vogel Peninsula,PNG

Boninites from Cape Vogel, PNG, are dominantly pyroxene-glass rocks, but many contain olivine, sometimes as refractory as Fo₉₄. We derive a parental magma for this suite (in equilibrium with Fo₉₄) which contains 20 wt.% MgO and is quartz-normative. This liquid is hydrous, and from petrographie evidence and whole rock H₂O⁺ values, we estimate it to contain 2–3 wt.% H₂O. These data suggest olivine fractionation and primary magmatic water are important in boninite genesis, but both are often obscured by later alteration. The derived parental magma has probably formed at 1,250–1,300° C and low pressures (< ?10kB) and is similar to those which gave rise to olivine-clinoenstatite phyric boninites from New Caledonia and from Howqua, Australia, and possibly to a proposed parental magma for the Bushveld Complex.     

Petrological and Os Isotopic Characteristics of Zedong Peridotites in the Eastern Yarlung–Zangbo Suture in Tibet

The Zedong ophiolites in the eastern Yarlung–Zangbo suture zone of Tibet represent a mantle slice of more than 45 km~2. This massif consists mainly of mantle peridotites, with lesser gabbros, diabases and volcanic rocks. The mantle peridotites are mostly harzburgite, lherzolite; a few dike-like bodies of dunite are also present. Mineral structures show that the peridotites experienced plastic deformation and partial melting. Olivine(Fo89.7–91.2), orthopyroxene(En_(88–92)), clinopyroxene(En_(45–49) Wo_(47–51) Fs_(2–4)) and spinel [Mg~#=100×Mg/(Mg+Fe)]=49.1–70.7; Cr~#=(100×Cr/(Cr+Al)=18.8–76.5] are the major minerals. The degree of partial melting of mantle peridotites is 10%–40%, indicating that the Zedong mantle peridotites may experience a multi–stage process. The peridotites are characterized by depleted major element compositions and low REE content(0.08–0.62 ppm). Their "spoon–shaped" primitive–mantle normalized REE patterns with(La/Sm)_N being 0.50–6.00 indicate that the Zedong ultramafic rocks belong to depleted residual mantle rocks. The PGE content of Zedong peridotites(18.19–50.74 ppb) is similar with primary mantle with Pd/Ir being 0.54–0.60 and Pt/Pd being 1.09–1.66. The Zedong peridotites have variable, unradiogenic Os isotopic compositions with ~(187)Os/~(188)Os=0.1228 to 0.1282. A corollary to this interpretation is that the convecting upper mantle is heterogeneous in Os isotopes. All data of the Zedong peridotites suggest that they formed originally at a mid-ocean ridge(MOR) and were later modified in supra–subduction zone(SSZ) environment.     

The composition of melt and fluid inclusions in spinel of peridotite xenoliths from Avacha volcano (Kamchatka)

This work considers the studies of melt and fluid inclusions in spinel of ultramafic rocks in the mantle wedge beneath Avacha volcano (Kamchatka). The generations of spinel were identified: 1 is spinel (Sp-I) of the “primary” peridotites, has the highest magnesium number (#0.69–0.71), highest contents of Al₂O₃ and lowest contents of Cr₂O₃ (26.2–27.1 and 37.5–38.5 wt %, respectively), and the absence in it of any fluid and melt inclusions; 2 is spinel (Sp-II) of the recrystallized peridotites, has lower magnesium number (Mg# 0.64–0.61) and the content of Al₂O₃ (18–19 wt %), a higher content of Cr₂O₃ (45.4–47.2 wt %) and the presence of primary fluid inclusions; 3 is spinel (Sp-III) that is characterized by the highest content of Cr₂O₃ (50.2–55.4 wt %), the lowest content of Al₂O₃ (13.6–16.6 wt %), and the presence of various types of primary melt inclusions. The data obtained indicate that metasomatic processing of “primary” peridotites occurred under the influence of high concentrated fluids of mainly carbonate-water-chloride composition with influx of the following petrogenic elements: Si, Al, Fe, Ca, Na, K, S, F, etc. This process was often accompanied by a local melting of the metasomatized substrate at a temperature above 1050°C with the formation of melts close to andesitic.     

Petrogenetic implications of ophiolitic chromite from Rutland Island, Andaman—a boninitic parentage in supra-subduction setting

Chromites occurring in different modes have been characterized from ophiolites of Rutland Island, a part of Burma-Andaman-Java subduction complex in the Bay of Bengal. Chromite mainly occurs as massive chromitite pods in mantle ultramafic tectonite and as thin massive chromitite bands together with minor disseminations in crustal ultramafic cumulate. Other than pods chromite also appears as: (a) anhedral restitic grains, (b) strings occurring as exsolved phases and as (c) symplectitic intergrowth with orthopyroxene in mantle tectonite. The chromites occurring as massive chromitite pods and bands contain high Cr (Cr#—73 to 80). Restitic chromite grains in mantle ultramafics are high-Mg (Mg#—58), high-Al (Al₂O₃—34 wt.%) and intermediate-Cr (Cr#—37) chromites. The bivariant plots of TiO₂ wt.% vs 100Cr#, Mg# vs Cr# and Cr-Al-Fe³⁺ ternary discrimination diagram show that the massive and disseminated chromites fall in the boninitic field. The (Al₂O₃)_melt and (FeO/MgO)_melt values for the massive chromitites are estimated as 10 wt.% to 11 wt.% and 0.67–1.78 respectively, corroborating a boninitic parentage. Massive chromitite on Fe²⁺/Fe³⁺ vs Al₂O₃ wt.% and TiO₂ wt.% vs Al₂O₃ wt.% plots occupy mainly the field of supra-subduction zone peridotites. High-Mg olivine (Fo_91?93), high-Mg orthopyroxene (En_～90) and high-Cr chromites of Rutland ophiolite are all supportive of boninitic source at supra-subduction zone setting. ⁵⁷Fe Mössbauer study of chromite of beach placer shows that chromites occur in partly inverse spinel structure with iron distribution as Fe³⁺(A)Fe²⁺(A)Fe²⁺(B) which might be a result of oxidation. The olivine-spinel geothermometry shows 650–700°C re-equilibration temperature which is much lower than near crystallization temperature (950–1,050°C) derived from orthopyroxene-clinopyroxene assemblage. At supra-subduction setting an oxidizing hydrous fluid derived from subducting slab might have a major influence during the formation of Rutland ophiolite in this part of Burma-Java subduction complex.     

Coexistence of the moderately refractory and fertile mantle beneath the eastern Central Asian Orogenic Belt

Relative to the North China Craton, the subcontinental lithospheric mantle (SCLM) beneath the Central Asian Orogenic Belt is little known. Mantle-derived peridotite xenoliths from the Cenozoic basalts in the Xilinhot region, Inner Mongolia, provide samples of the lithospheric mantle beneath the eastern part of the belt. The xenoliths are predominantly lherzolites with minor harzburgites, and can be subdivided into three groups, based on the REE patterns of clinopyroxenes. Group 1 peridotites (LREE-enriched), with low modal Cpx (3–7%), high Mg^# in olivine (> 90.6) and Cr^# in spinel (> 43.8), low whole-rock CaO + Al₂O₃ contents (1.62–3.22 wt.%) and estimated temperatures of 1043–1126 °C, represent moderately refractory SCLM that has experienced carbonatite-related metasomatism. Group 2 peridotites (LREE-depleted), with high modal Cpx (9–13%), low Mg^# in olivine (< 90.6) and Cr^# in spinel (< 20.0), high whole-rock CaO + Al₂O₃ contents (4.93–6.37 wt.%) and estimated temperatures of 814–970 °C, show affinity with Phanerozoic fertile SCLM that has undergone silicate-related metasomatism. Group 3 peridotites (convex-upward REE patterns), show wide ranges of olivine-Mg^# (88.4–90.6), spinel-Cr^# (11.5–47.6), and modal Cpx (3–14%) that overlap Groups 1 and 2. Their spinels have high TiO₂ contents (> 0.41 wt.%), implying involvement of reactions between melt and peridotites. The estimated temperatures of Group 3 (1033–1156 °C) are similar to those of Group 1. We suggest that the pre-existing moderately refractory lithospheric mantle (i.e., Group 1) beneath the eastern part of the Central Asian Orogenic Belt was strongly penetrated by upwelling asthenospheric material, and the cooling of this material produced fertile lithospheric mantle (i.e., Group 2). The present lithospheric mantle of this area consists of interspersed volumes of younger fertile and older more refractory lithosphere, with the fertile type dominating the shallower levels of the mantle.