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.     

The water content and hydrogen isotope composition of continental lithospheric mantle and mantle-derived mafic igneous rocks in eastern China

The water contents of minerals and whole-rock in mantle-derived xenoliths from eastern China exhibit large variations and are generally lower than those from other on- and off-craton lithotectonic units. Nevertheless, the water contents of mineral and whole-rock in Junan peridotite xenoliths, which sourced from the juvenile lithospheric mantle, are generally higher than those elsewhere in eastern China. This suggests that the initial water content of juvenile lithospheric mantle is not low. There is no obvious correlation between the water contents and Mg^# values of minerals in the mantle xenoliths and no occurrence of diffusion profile in pyroxene, suggesting no relationship between the low water content of mantle xenolith and the diffusion loss of water during xenolith ascent with host basaltic magmas. If the subcontinental lithospheric mantle (SCLM) base is heated by the asthenospheric mantle, the diffusion loss of water is expected to occur. On the other hand, extraction of basaltic melts from the SCLM is a more efficient mechanism to reduce the water content of xenoliths. The primary melts of Mesozoic and Cenozoic basalts in eastern China have water contents, as calculated from the water contents of phenocrysts, higher than those of normal mid-ocean ridge basalts (MORB). The Mesozoic basalts exhibit similar water contents to those of island arc basalts, whereas the Cenozoic basalts exhibit comparable water contents to oceanic island basalts and backarc basin basalts with some of them resembling island arc basalts. These observations suggest the water enrichment in the mantle source of continental basalts due to metasomatism by aqueous fluids and hydrous melts derived from dehydration and melting of deeply subducted crust. Mantle-derived megacrysts, minerals in xenoliths and phenocrysts in basalts from eastern China also exhibit largely variable hydrogen isotope compositions, indicating a large isotopic heterogeneity for the Cenozoic SCLM in eastern China. The water content that is higher than that of depleted MORB mantle and the hydrogen isotope composition that is deviated from that of depleted MORB mantle suggest that the Cenozoic continental lithospheric mantle suffered the metasomatism by hydrous melts derived from partial melting of the subducted Pacific slab below eastern China continent. The metasomatism would lead to the increase of water content in the SCLM base and then to the decrease of its viscosity. As a consequence, the SCLM base would be weakened and thus susceptible to tectonic erosion and delamination. As such, the crust-mantle interaction in oceanic subduction channel is the major cause for thinning of the craton lithosphere in North China.     

Water contents of clinopyroxenes from sub‐arc mantle peridotites

One poorly constrained reservoir of the Earth's water budget is that of clinopyroxene in metasomatised, mantle peridotites. This study presents reconnaissance Sensitive High‐Resolution, Ion Microprobe–Stable Isotope (SHRIMP–SI) determinations of the H₂O contents of (dominantly) clinopyroxenes in rare mantle xenoliths from four different subduction zones, i.e. Mexico, Kamchatka, Philippines, and New Britain (Tabar‐Feni island chain) as well as one intra‐plate setting (western Victoria). All of the sub‐arc xenoliths have been metasomatised and carry strong arc trace element signatures. Average measured H₂O contents of the pyroxenes range from 70 ppm to 510 ppm whereas calculated bulk H₂O contents range from 88 ppm to 3 737 ppm if the variable presence of amphibole is taken into account. In contrast, the intra‐plate, continental mantle xenolith from western Victoria has higher water contents (3 447 ppm) but was metasomatised by alkali and/or carbonatitic melts and does not carry a subduction‐related signature. Material similar to the sub‐arc peridotites can either be accreted to the base of the lithosphere or potentially be transported by convection deeper into the mantle where it will lose water due to amphibole breakdown.     

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

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

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.     

Deformation and seismic anisotropy of the lithospheric mantle in the southeastern Carpathians inferred from the study of mantle xenoliths

Peridotite xenoliths with a broad range of textures provides evidence for consistent microstructural evolution in a vertical transect of the shallow lithospheric mantle (35–55 km depth) beneath the Persani Mountains, SE Carpathians, Romania, due to ongoing plate convergence in the Carpathian Arc nearby. The recrystallized grain size, crystal preferred orientations strength, and resulting seismic anisotropy vary continuously and display a strong correlation to equilibrium temperatures, suggesting a continuous change in deformation conditions with depth. The shallowmost xenoliths have microstructures typical of high stress deformation, marked by strong recrystallization to fine grain sizes, which results in weak crystal preferred orientations and anisotropy. The deepest xenoliths have coarse-grained porphyroclastic microstructures and strong crystal preferred orientations. Replacive orthopyroxene structures, consuming olivine, and high H₂O concentrations in the pyroxenes are observed in some xenoliths indicating limited percolation of fluids or volatile-rich melts. Despite the high stress deformation and high H₂O contents in some of the studied xenoliths, analysis of olivine crystallographic orientations indicates that [100] slip systems, rather than “wet” [001] accommodate most of the deformation in all samples. Seismic anisotropy estimated from the measured olivine and pyroxene crystal preferred orientations suggests that the strike-parallel fast SKS polarization directions and ~ 1 s delay times measured in the SE Carpathians are likely the consequence of convergence-driven belt-parallel flow in the lithospheric mantle.     

Possible sub-arc origin of podiform chromitites

Abstract The sub-arc mantle condition possibly favors the formation of podiform chromitites. The Cr/(Cr + Al) atomic ratio (= Cr#) of their chromian spinel frequently is higher than 0.7, which is comparable with the range for arc-related primitive magmas. This almost excludes the possibility of their sub-oceanic origin, because both oceanic peridotites and MORB have chromian spinel with the Cr# < 0.6. Precipitation of chromitite and associated dunite enhances a relative depletion of high-field strength elements (HFSE) to large-ion lithophile elements (LILE), one of chemical characteristics of arc magmas, for the involved magma. This cannot alter completely, however, the MORB to the arc-type magma, especially for Ti and Zr. The presence of chromitite xenoliths, similar both in texture and in chemistry to podiform chromitites of some ophiolitic complexes, in some Cenozoic alkali basalts from the southwest Japan arc indicates directly that the upper mantle beneath the Japan arcs has chromitites.     

Evidence of mantle metasomatism and heterogeneity from peridotite inclusions of northeastern Brazil and Paraguay

Textural-petrographic features, major and trace elements and mineral chemistry are reported for spinel-peridotite xenoliths from northeastern Brazil (NE-suite) and Paraguay (PY-suite).Variation trends defined by bulk rock and mineral chemistry are consistent with the effects of variable degree of high-pressure melting for both suites.The PY-suite strongly differs from the NE-suite by its very high contents of incompatible elements. This different whole-rock chemistry is related to the presence of glassy-microcrystalline blebs which are interpreted as remains of pre-existing hydrous phases of metasomatic origin. The difference between the two suites is also recorded in the chemistry of pyroxenes and spinels, which develop along different variation patterns.Although the suites partially overlap in their ranges ofmg_opx (Mg/(Fe²⁺ + Fe³⁺) ratio in orthopyroxenes), the PY-suite is, on the average, moremg_opx rich (residual) than the NE-suite. Within the PY-suite a rough positive correlation exists between degree of residuality and degree of metasomatic effects.The sharp differences between the NE-suite and the PY-suite imply mantle heterogeneity on regional scale, whereas the variability within each suite is essentially related to different degrees of melting and/or metasomatism and imply mantle heterogeneity on local scale.     

A review of mantle xenoliths and their role in diamond exploration

An historical introduction to the geotherm and its significance for the existence of a diamond window at the base of the peridotite lithosphere is followed by a brief survey of types of mantle zenoliths (low T, high T and metasomatized peridotites, megacrysts or discrete nodules, eclogites and less common varieties). The similarities of eclogite xenoliths to the subducted eclogites with graphitized diamonds in the peridotite massif of Beni Bousera, northern Morocco, are reviewed. Diamond-bearing peridotite (Archaean harzburgite and lherzolite) and eclogite xenoliths are rare, having suffered excessive disaggregation. They do not necessarily relate proportionately to the types of diamonds in the host kimberlite/lamproite.Batches of single mineral species from disaggregated diamondiferous xenoliths, particularly garnets, form a realistic approach to diamond exploration. Nickel thermometry applied to Cr pyropes, developed by Griffin et al. (1989) Contr. Miner. Petrol. 103, 199–203, and barometry dependent upon Cr content in notional coexisting spinels, provide a realistic appreciation of the extent of the diamond window. Sodium and K pressure “indicators” in eclogitic garnets and clinopyroxenes are reviewed, but estimates are affected by mantle processes (metasomatism) and amounts of coexisting P and Ti.Metasomatic processes in the basal lithosphere are sourced in the underlying asthenospheric (megacryst) magmas. Depending on the degree and type of interaction they can result in the destruction of ancient diamonds or the growth of new peridotitic diamonds. Partial destruction or replacement of mineral indicators may also result and Cr garnets acquire distinctive quantifiable trace element signatures. High T minerals encapsulated in diamond are either relict from former ambient high T conditions or the result of localized thermal highs emanating from asthenospheric magmas (or plume/diapir).It is concluded that the fullest significance of the geochemistry (sensuo lato) of the diamondiferous debris erupted by kimberlites and lamproites, can only be made by reference to complementary geophysical, structural and isotopic studies of the surrounding cratonic country rocks. Thus, tectonothermal events which punctuate the varied evolutionary histories of cratons—plume migration, rifting, subduction/overthrusting, delamination, cratonization, flood basalt generation, regional metamorphism and metasomatism, etc.—can be manifested in the deep lithosphere environment, and cannot be divorced from questions of diamond formation and survival.     

On water in nominally anhydrous minerals from mantle peridotites and magmatic rocks

Trace amount of water associated with the lattice defects of nominally anhydrous minerals (NAMs) can be measured using Fourier transform infrared spectroscopy (FTIR) and secondary ion mass spectrometry (SIMS). Lots of data on water in NAMs from different lithologies, especially mantle peridotite xenoliths, have been published. The water distribution in olivine from peridotite xenoliths often displays a diffusion profile with high water concentration in the core and low at the rim, which indicates water loss via diffusion during the ascent of host magma. On the other hand, water is homogeneously distributed in pyroxene and its concentration is typically interpreted to represent a mantle value. The water concentration of magma in equilibrium with NAM can be estimated using specific partition coefficient, from which the water content of parental magma and the mantle source can be inferred. The accuracy of this method, however, depends on the selection of appropriate partition coefficient for the system. Using hydrogen isotope compositions and H₂O/Ce ratios of mantle NAMs, water source regions can be traced and water heterogeneity can be mapped in the upper mantle. Water plays an important role in the stability of cratonic mantle. The water contents and vertical distribution patterns can be significantly different among different cratonic mantles, which may result from different geologic activities. However, the mantle-plume interaction may not necessarily result in significant change of water content in cratonic mantle. The estimation of the water content in the upper mantle is still largely based on geochemical models due to the limitations of data on water in mantle NAMs.     

Element diffusion ability in metasomatic agents and its effect on chemical characteristics of metasomatized peridotites

The partial melting and metasomatism are two most important geological processes of changing chemical compositions of mantle. Extracting partial melt from primitive mantle leads residual mantle to deplete in- compatible elements, whereas the metasomatism …     

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.     

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.     

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.     

Storage and interaction of compositionally heterogeneous magmas from the 1986 eruption of Augustine Volcano, Alaska

Compositional heterogeneity (56–64 wt% SiO₂ whole-rock) in samples of tephra and lava from the 1986 eruption of Augustine Volcano, Alaska, raises questions about the physical nature of magma storage and interaction beneath this young and frequently active volcano. To determine conditions of magma storage and evolutionary histories of compositionally distinct magmas, we investigate physical and chemical characteristics of andesitic and dacitic magmas feeding the 1986 eruption. We calculate equilibrium temperatures and oxygen fugacities from Fe-Ti oxide compositions and find a continuous range in temperature from 877 to 947°C and high oxygen fugacities (ΔNNO=1–2) for all magmas. Melt inclusions in pyroxene phenocrysts analyzed by Fourier-transform infrared spectroscopy and electron probe microanalysis are dacitic to rhyolitic and have water contents ranging from <1 to ∼7 wt%. Matrix glass compositions are rhyolitic and remarkably similar (∼75.9–76.6 wt% SiO₂) in all samples. All samples have ∼25% phenocrysts, but lower-silica samples have much higher microlite contents than higher-silica samples. Continuous ranges in temperature and whole-rock composition, as well as linear trends in Harker diagrams and disequilibrium mineral textures, indicate that the 1986 magmas are the product of mixing between dacitic magma and a hotter, more mafic magma. The dacitic endmember is probably residual magma from the previous (1976) eruption of Augustine, and we interpret the mafic endmember to have been intruded from depth. Mixing appears to have continued as magmas ascended towards the vent. We suggest that the physical structure of the magma storage system beneath Augustine contributed to the sustained compositional heterogeneity of this eruption, which is best explained by magma storage and interaction in a vertically extensive system of interconnected dikes rather than a single coherent magma chamber and/or conduit. The typically short repose period (∼10 years) between Augustine's recent eruptive pulses may also inhibit homogenization, as short repose periods and chemically heterogeneous magmas are observed at several volcanoes in the Cook Inlet region of Alaska.     

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.

     

Mineral chemistry and petrogenesis of chromitites from the Khoy ophiolite complex,Northwestern Iran: Implications for aggregation of two ophiolites

The Khoy ophiolitic complex in Northwestern Iran is a part of the Tethyan ophiolite belt, and is divided into two sections: the Eastern ophiolite in Qeshlaq and Kalavanes (Jurassic–Cretaceous) and the Western ophiolite in Barajouk, Chuchak and Hessar (Late Cretaceous). Our chromitites can be clearly classified into two groups: high‐Al chromitites (Cr# = 0.38–0.44) from the Eastern ophiolite, and high‐Cr chromitites (Cr# = 0.54–0.72) from the Western ophiolite. The chromian spinels in high‐Al chromitite include primary mineral inclusions mainly as Na‐bearing diopside and pargasite with subordinate rutile and their formation was probably related to reaction between a MORB (mid‐ocean‐ridge basalt)‐like melt with depleted harzburgite, possibly in a back‐arc setting. Their host harzburgites contain clinopyroxene with higher contents of Al₂O₃, Na₂O, Cr₂O₃, and TiO₂ relative to Western harzburgites and are possibly residue after moderate partial melting (~15 %) whereas the Western harzburgite is residue after high partial melting (~25 %). The chromian spinel in the Western Khoy chromitites contains inclusions such as clinopyroxene, olivine and platinum group mineral‐bearing sulfides. These Western chromitites were possibly formed at two stages during arc growth and are divided into the moderately high‐Cr# chromitites (Barajouk and Hessar) and the high‐Cr# chromitites (Chuchak A and C). The former crystallized from island‐arc‐tholeiite (IAT) melts during reaction with the host depleted harzburgites, whereas the latter crystallized from boninitic melts (second stage melt) during reaction with highly depleted harzburgite in a supra‐subduction‐zone environment. Based on the mineral chemistry of chromian spinels, pyroxenes, and mineral inclusions, the chromitites and the host peridotites from the Eastern and Western Khoy ophiolites were formed in a back‐arc basin and arc‐related setting, respectively. The Khoy ophiolitic complex is a tectonic aggregate of the two different ophiolites formed in two different tectonic settings at different ages.     

Mantle–crust interactions during Variscan subduction in the Eastern Alps (Nonsberg–Ulten zone): geochronology and new petrological constraints

We have analyzed the Sm–Nd and Rb–Sr whole-rock and mineral isotope systematics of garnet peridotites and associated eclogites and migmatitic gneisses from the Nonsberg–Ulten zone of the Eastern Alps. The garnet peridotites include coarse-grained varieties, characterized by well-preserved to slightly modified mantle geochemical signatures, and finer-grained varieties enriched in amphibole and LILE. Hydration of some of the most strongly deformed, fine-grained peridotites by crustal fluids caused isotopic disequilibrium between the peridotite minerals, preventing accurate age determinations. The coarse-grained peridotites, the eclogites and the country migmatitic gneisses yield garnet–whole-rock and garnet–clinopyroxene Sm–Nd ages that indicate for all rock types an isotopic homogenization event at ca. 330 Ma. The similar ages suggest that all rock types shared a common history since the incorporation of the peridotites in the crust, and constrain the garnet-facies metamorphism of the peridotites, as well as partial melting of the crust, to an episode of crustal subduction at the end of the Variscan orogenic cycle.     

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

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

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.