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.     

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.     

Chemical characteristics of chromian spinel in plutonic rocks: Implications for deep magma processes and discrimination of tectonic setting

We summarize chemical characteristics of chromian spinels from ultramafic to mafic plutonic rocks (lherzolites, harzburgites, dunites, wehrlites, troctolites, olivine gabbros) with regard to three tectonic settings (mid‐ocean ridge, arc, oceanic hotspot). The chemical range of spinels is distinguishable between the three settings in terms of Cr# (= Cr/(Cr + Al) atomic ratio) and Ti content. The relationships are almost parallel with those of chromian spinels in volcanic rocks, but the Ti content is slightly lower in plutonics than in volcanics at a given tectonic environment. The Cr# of spinels in plutonic rocks is highly diverse; its ranges overlap between the three settings, but extend to higher values (up to 0.8) in arc and oceanic hotspot environments. The Ti content of spinels in plutonics increases, for a given lithology, from the arc to oceanic hotspot settings by mid‐ocean ridge on average. This chemical diversity is consistent with that of erupted magmas from the three settings. If we systematically know the chemistry of chromian spinels from a series of plutonic rocks, we can estimate their tectonic environments of formation. The spinel chemistry is especially useful in dunitic rocks, in which chromian spinel is the only discriminating mineral. Applying this, discordant dunites cutting mantle peridotites were possibly precipitated from arc‐related magmas in the Oman ophiolite, and from an intraplate tholeiite in the Lizard ophiolite, Cornwall.     

Detrital chromian spinels from beach placers of Andaman Islands,India: A perspective view of petrological characteristics and variations of the Andaman ophiolite

Along the east coast of the Andaman Islands, abundant detrital chromian spinels frequently occur in black sands at the confluence of streams meeting the Andaman Sea. The mineral chemistry of these detrital chromian spinels has been used in reconstructing the evolutionary history of the Andaman ophiolite. The chromian spinels show wide variation in compositional parameters such as Cr# [= Cr/(Cr + A1) atomic ratio] (0.13–0.91), Mg# [= Mg/(Mg + Fe²⁺) atomic ratio] (0.23–0.76), and TiO₂ (<0.05–3.9 wt%). The YFe³⁺[= 100Fe³⁺/(Cr + A1 + Fe³⁺) atomic ratio] is remarkably low (usually <10 except for south Andaman). The ranges of chemical composition of chromian spinels are different in each locality. The spinel compositions show very depleted signatures over the entire island, which suggests that all massifs in the Andaman ophiolite were affected under island‐arc conditions. Although the degree of depletion varies in different parts of the island, a directional change in composition of the detrital chromian spinels from south to north is evident. Towards the north the detrital chromian spinels point to less‐depleted source rocks in contrast to relatively more depleted towards the south. The possibilities to explain this directional change are critically discussed in the context of the evolution of Andaman ophiolite.     

Chromite in the mantle section of the Oman ophiolite: A new genetic model

Abstract   This paper reviews the compositional data (major elements, platinum group element [PGE] concentrations, Os- and O-isotopes) for chromites from the mantle section of the Oman ophiolite. Chromites in chromitite from the Oman ophiolite lie on a compositional spectrum between high-Cr♯, boninite-like and low-Cr♯, mid-oceanic ridge basalt-like end-members. The high-Cr♯ end-member is low in Ti, has a fractionated PGE pattern and is enriched in iridium group-platinum group elements (IPGE). The low-Cr♯ end-member has higher Ti and an unfractionated PGE pattern. The compositional variation in the chromitites reflects their crystallization from a range of different melt compositions. It is proposed that this wide variation in melt compositions was produced by the process of a melt–rock reaction, whereby a basaltic melt has reacted with harzburgitic mantle to yield successively more Cr-rich melts. In contrast to previous models, this approach does not require a change in the tectonic environment to explain the different chromite types.     

Podiform chromitites in the lherzolite-dominant mantle section of the Isabela ophiolite, the Philippines

Abstract The Isabela ophiolite, the Philippines, is characterized by a lherzolite‐dominant mantle section, which was probably formed beneath a slow‐spreading mid‐ocean ridge. Several podiform chromitites occur in the mantle section and grade into harzburgite to lherzolite. The chromitites show massive, nodular, layered and disseminated textures. Clinopyroxene (±orthopyroxene/amphibole) inclusions within chromian spinel (chromite hereafter) are commonly found in the massive‐type chromitites. Large chromitites are found in relatively depleted harzburgite hosts having high‐Cr? (Cr/(Cr + Al) atomic ratio = ～0.5) chromite. Light rare earth element (LREE) contents of clinopyroxenes in harzburgites near the chromitites are higher than those in lherzolite with low‐Cr? chromite, whereas heavy REE (HREE) contents of clinopyroxenes are lower in harzburgite than in lherzolite. The harzburgite near the chromitites is not a residual peridotite after simple melt extraction from lherzolite but is formed by open‐system melting (partial melting associated with influx of primitive basaltic melt of deeper origin). Clinopyroxene inclusions within chromite in chromitites exhibit convex‐shaped REE patterns with low HREE and high LREE (+Sr) abundances compared to the host peridotites. The chromitites were formed from a hybridized melt enriched with Cr, Si and incompatible elements (Na, LREE, Sr and H₂O). The melt was produced by mixing of secondary melts after melt–rock interaction and the primitive basaltic melts in large melt conduits, probably coupled with a zone‐refining effect. The Cr? of chromites in the chromitites ranges from 0.65 to 0.75 and is similar to those of arc‐related magmas. The upper mantle section of the Isabela ophiolite was initially formed beneath a slow‐spreading mid‐ocean ridge, later introduced by arc‐related magmatisms in response to a switch in tectonic setting during its obduction at a convergent margin.     

Complete mantle section of a slow-spreading ridge-derived ophiolite: An example from the Isabela ophiolite in the Philippines

Abstract   The Isabela ophiolite shows a complete ophiolite sequence exposed along the eastern coast of northern Luzon, the Philippines. It forms the Cretaceous basement complex for the northeastern Luzon block. This ophiolite is located at the northern end of a trail of ophiolites and ophiolitic bodies along the eastern margin of the Philippine Mobile Belt. This paper presents new findings regarding the nature and characteristics of the Isabela ophiolite. Peridotites from the Isabela ophiolite are relatively fresh and are composed of spinel lherzolites, clinopyroxene-rich harzburgites, depleted harzburgites and dunites. The modal composition, especially the pyroxene content, defines a northward depletion trend from fertile lherzolite to clinopyroxene-rich harzburgites and more refractory harzburgites. Variation in modal composition is accompanied by petrographic textural variations. The chromium number of spinel, an indicator of the degree of partial melting, concurs with petrographic observations. Furthermore, the Isabela ophiolite peridotites are similar in spinel and olivine major-element geochemistry and clinopyroxene rare earth-element composition to abyssal peridotites from modern mid-oceanic ridges. Petrological and mineral compositions suggest that the Isabela ophiolite is a transitional ophiolite subtype, with the fertile lherzolites representing lower sections of the mantle column that are usually absent in most ophiolitic massifs. The occurrence of the fertile peridotite presents a rare opportunity to document the lower sections of the ophiolitic mantle. The variability in composition of the peridotites in one continuous mantle section may also represent a good analogy of the melting column in the present-day mid-oceanic ridges.     

Mineral chemical composition and geodynamic significance of peridotites from Nain ophiolite,central Iran

The peridotites from north of the town of Nain in central Iran consist of clinopyroxene-bearing harzburgite and lherzolite with small lenses of dunite and chromitite pods. The lherzolite contains aluminous spinel with a Cr number (Cr^# = Cr/[Cr + Al]) of 0.17. The Cr number of spinels in harzburgite and chromitite is 0.38–0.42 and 0.62, respectively. This shows that the lherzolite and harzburgite resulted from <18% of partial melting of the source materials. The estimated temperature is 1100 ± 200 °C for peridotites, the estimated pressure is <15 ± 2.3 kbar for harzburgites and >16 ± 2.3 kbar for lherzolites and estimated fo₂ is 10^?1±0.5 for peridotites. Discriminant geochemical diagrams based on mineral chemistry of harzburgites indicate a supra-subduction zone (SSZ) to mid-oceanic ridge (MOR) setting for these rocks. On the basis of their Cr^#, the harzburgite and lherzolite spinels are analogous to those from abyssal peridotites and oceanic ophiolites, whereas the chromites in the chromitite (on the basis of Cr^# and boninitic nature of parental melts) resemble those from SSZ ophiolitic sequences. Therefore, the Nain ophiolite complex most likely originated in an oceanic crust related to supra-subduction zone, i.e. back arc basin. Field observations and mineral chemistry of the Nain peridotites, indicating the suture between the central Iran micro-continent (CIM) block and the Sanandaj–Sirjan zone, show that these peridotites mark the site of the Nain–Baft seaway, which opened with a slow rate of ocean-floor spreading behind the Mesozoic arc of the Sanandaj–Sirjan zone as a result of change of Neo Tethyan subduction régime during middle Cretaceous.     

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

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

Evolution of lithospheric mantle in the north of Nain‐Baft oceanic crust (Neo‐Tethyan ophiolite of Ashin,Central Iran)

This study is focused on a plagioclase‐bearing spinel lherzolite from Chah Loqeh area in the Neo‐Tethyan Ashin ophiolite. It is exposed along the west of left‐lateral strike‐slip Dorouneh Fault in the northwest of Central‐East Iranian Microcontinent. Mineral chemistry (Mg#^olivine < ~ 90, Cr#^{clinopyroxene} < ~ 0.2, Cr#^spinel < ~ 0.5, Al₂O₃^{orthopyroxene} > ~ 2.5 wt%, Al₂O₃^{clinopyroxene} > ~ 4.5 wt%, Al₂O₃^spinel > ~ 41.5 wt%, Na₂O^{clinopyroxene} > ~ 0.11 wt%, and TiO₂^{clinopyroxene} > ~ 0.04 wt%) confirms Ashin lherzolite was originally a mid‐oceanic ridge peridotite with low degrees of partial melting at spinel‐peridotite facies in a lithospheric mantle level. However, some Ashin lherzolites record mantle upwelling and tectonic exhumation at plagioclase‐peridotite facies during oceanic extension and diapiric motion of mantle along Nain‐Baft suture zone. This mantle upwelling is evidenced by some modifications in the modal composition (i.e. subsolidus recrystallization of plagioclase and olivine between pyroxene and spinel) and mineral chemistry (e.g. increase in TiO₂ and Na₂O of clinopyroxene, and TiO₂ and Cr# of spinel and decrease in Mg# of olivine), as a consequence of decompression during a progressive upwelling of mantle. Previous geochronological and geochemical data and increasing the depth of subsolidus plagioclase formation at plagioclase‐peridotite facies from Nain ophiolite (~ 16 km) to Ashin ophiolite (~ 35 km) suggest a south to north closure for the Nain‐Baft oceanic crust in the northwest of Central‐East Iranian Microcontinent.     

Trace element characteristics of the fluid liberated from amphibolite-facies slab: Inference from the metamorphic sole beneath the Oman ophiolite and implication for boninite genesis

Major and trace element compositions of amphibolites and quartzose rocks in the 230-m-thick metamorphic sole underlying the mantle section of the Oman ophiolite in Wadi Tayin area were determined to investigate the chemical characteristics of the hydrous fluid released from subducted amphiboltie-facies slab. The fluid-immobile element compositions indicate that protoliths of these rocks are mid-ocean ridge basalt-like tholeiite and deep-sea chert, which is consistent with the idea that these rocks represent Tethyan oceanic crust overridden during the early, intraoceanic thrusting stage of the Oman ophiolite emplacement. The rare-earth element (REE) and high field-strength element concentrations of the amphibolites show limited variations, within a factor of two except for a few evolved samples, throughout transect of the sole. On the other hand, concentrations of fluid-mobile elements, especially B, Rb, K and Ba, in amphibolites are highly elevated in upper 30 m of the sole (> 600 °C in peak metamorphic temperature), suggesting the equilibration with evolved, B-Rb-K-Ba-rich fluids during prograde metamorphism. The comparison with amphibolites in the lower 150 m (500 to 550 °C) demonstrates that the trace element spectra of the fluids equilibrated with the high-level amphibolites may vary as a function of metamorphic temperature. The fluids are characterized by striking enrichments of B, Rb, K and Ba and moderate to minor enrichments of Sr, Li, Be and Pb. At higher temperature (up to 700 °C), the fluids become considerably enriched in light REE and Nb in addition to the above elements. The estimated trace element spectra of the fluids do not coincide with the compositions of basalts from matured intra-oceanic arcs, but satisfactorily explain the characteristics of the low-Pb andesites and boninites found in the Oman ophiolite. Compositional similarity between the boninites of Oman and other localities suggests that the fluids estimated here well represent the amphibolite-derived fluids involved in the magmatism of immatured, hot, shallow subduction zones.     

蛇绿岩研究现状及华南蛇绿岩问题

蛇绿岩概念自上世纪70年代提出以来,就成为确定古板块边界的重要证据,具有重要大地构造学意义,一直是地质学家研究的热点之一。近年来,随着地球化学技术的发展以及深海钻探计划和大洋钻探计划的实施,世界各地蛇绿岩研究不断深入,取得了很大的发展,同时也提出了很多新的问题。本文主要论述了蛇绿岩研究的最新动态,并对华南蛇绿岩的研究进展进行了分析梳理,对存在的一些问题作了初步讨论。     

Slab-fluid metasomatism in the Early Paleozoic forearc mantle deduced from the Motai serpentinites,South Kitakami Belt,northeast Japan

The present study examines the petrology and geochemistry of the Early Paleozoic Motai serpentinites, the South Kitakami Belt, northeast Japan, to reveal the subduction processes and tectonics in the convergent margin of the Early Paleozoic proto-East Asian continent. Protoliths of the serpentinites are estimated to be harzburgite to dunite based on the observed amounts of bastite (orthopyroxene pseudomorph). Relic chromian spinel Cr# [=Cr/(Cr + Al)] increases with decreasing amount of bastite. The compositional range of chromian spinel is similar to that found in the Mariana forearc serpentinites. This fact suggests that the protoliths of the serpentinites are depleted mantle peridotites developed beneath the forearc regions of a subduction zone. The Motai serpentinites are divided into two types, namely, Types 1 and 2 serpentinites; the former are characterized by fine-grained antigorite and lack of olivine, and the latter have coarse-grained antigorite and inclusion-rich olivine. Ca-amphibole occurs as isolated crystals or vein-like aggregates in the Type 1 serpentinites and as needle-shaped minerals in the Type 2 serpentinites. Ca-amphibole of the Type 1 serpentinites is more enriched in LILEs and LREEs, suggesting the influence of hydrous fluids derived from slabs. By contrast, the mineral assemblage, mineral chemistry, and field distribution of the Type 2 serpentinites reflect the thermal effect of contact metamorphism by Cretaceous granite. The Ca-amphibole of the Type 1 serpentinites is different from that of the Hayachine–Miyamori Ophiolite in terms of origin; the latter was formed by the infiltration of melts produced in an Early Paleozoic arc–backarc system. Chemical characteristics of the Ca-amphibole in the ultramafic rocks in the South Kitakami Belt reflect the tectonics of an Early Paleozoic mantle wedge, and the formation of the Motai metamorphic rocks in the forearc region of the Hayachine–Miyamori subduction zone system, which occurred at the Early Paleozoic proto-East Asian continental margin.     

Tectonic implication of Lower Cretaceous chromian spinel-bearing sandstones in Japan and Korea

Abstract In Japan and Korea, some Lower Cretaceous terrigenous clastic rocks yield detrital chromian spinels. These chromian spinels are divided into two groups: low-Ti and high-Ti. The Sanchu Group and the Yuno Formation in Japan have both groups, whereas the Nagashiba Formation in Japan and the Jinju Formation in Korea have only the low-Ti spinels. High-Ti spinels are thought to have originated in intraplate-type basalt. Low-Ti spinels (higher than 0.6 Cr#) were probably derived from peridotites, which are highly correlated with an arc setting derivation and possibly with a forearc setting derivation. Low-Ti spinels are seen in the Sanchu Group, the Nagashiba Formation and the Jinju Formation. Low-Ti spinels from the Yuno Formation are characterized by low Cr# (less than 0.6) and these chromian spinels appear to have been derived from oceanic mantle-type peridotite, including backarc. According to maps reconstructing the pre-Sea of Japan configuration of the Japanese Islands and the Korean Peninsula, the Korean Cretaceous basin was comparatively close to the Southwest Japan depositional basins. It is possible that these Lower Cretaceous systems were sediments mainly in the forearc and partly in the backarc regions. The peridotite might have infiltrated along major tectonic zones such as the Kurosegawa Tectonic Zone (= serpentinite melange zone) in which left lateral movement prevailed during the Early Cretaceous.     

Neoproterozoic podiform chromitites in serpentinites of the Abu Meriewa–Hagar Dungash district, Eastern Desert, Egypt: Geotectonic implications and metamorphism

Podiform chromitites hosted in serpentinites (after harzburgite and dunite) and talc‐carbonate rocks from the Abu Meriewa–Hagar Dungash district (MHD), Eastern Desert of Egypt, together with metagabbros, pillow metavolcanics, and metasediments, form an ophiolitic mélange formed during the Neoproterozoic Pan‐African Orogeny. The chromitites show massive, disseminated, and nodular textures. Chromite cores in chromitites have high and restricted ranges of Cr# (0.65–0.75) and Mg# (0.64–0.83), implying primary compositions not affected by metamorphism. Therefore, they are used as reliable indicators of parent magma composition and tectonic affinities of these highly metamorphosed rocks. On the contrary, the altered rims are high‐Cr, low‐Fe³⁺ spinel (rather than ferritchromit) enriched in Cr, Fe, and Mn, and depleted in Al and Mg (Cr# = 0.75–0.97, Mg# = 0.29–0.79), due to equilibration with interstitial silicates during regional metamorphism up to transitional greenschist–amphibolite facies at about 500–550°C. The primary chromite compositions suggest derivation from a high‐Mg tholeiitic, to possibly boninitic, parental magma in a supra‐subduction zone (arc–marginal basin) environment, similar to the spatially associated metavolcanic rocks. The MHD chromitites are most probably formed by melt–rock interaction mechanisms. The high Cr# of the investigated chromites suggests high degrees of partial melting of a depleted harzburgite source by interaction with primitive basaltic melt of deeper origin followed by mixing. Such Cr‐rich chromites are common in chromitites from the Eastern Desert of Egypt, implying broad thermal anomalies, possibly linked to an important geodynamic feature of the Arabian–Nubian Shield (ANS) evolution. This could revive interest in models that involve asthenospheric uprise, related to plume interaction or most probably due to oblique convergence of arc terranes during early evolution of the ANS.     

Comparison of eastern paleo-Tethyan ophiolites and its geodynamic significance--Evidence from Dur''ngoi ophiolite

Nd-Pb isotopic geochemistry of metabasalt from Dur'ngoi ophiolite, Qinghai Province, NW China reveals the presence of DMM mixing with EMIl components in its upper mantle source, which is comparable with present Indian MORB. Comparisons indicate that the geochemistry, chronology and source characteristics of Dur'ngoi ophiolite coincide with Paleo-tethyan ophiolites from "Sanjiang" area. Together with evidences from regional geology in adjacent areas, this study proves that independent paleo-tethyan basins evolved contemporarily,the dynamics of which is attributed to the interaction of mantle plume with over-riding lithosphere.     

Provenance of sandstones from the Wakino Subgroup of the Lower Cretaceous Kanmon Group, northern Kyushu, Japan

Abstract The Wakino Subgroup is a lower stratigraphic unit of the Lower Cretaceous Kanmon Group. Previous studies on provenance of Wakino sediments have mainly concentrated on either petrography of major framework grains or bulk rock geochemistry of shales. This study addresses the provenance of the Wakino sandstones by integrating the petrographic, bulk rock geochemistry, and mineral chemistry approaches. The proportions of framework grains of the Wakino sandstones suggest derivation from either a single geologically heterogeneous source terrane or multiple source areas. Major source lithologies are granitic rocks and high‐grade metamorphic rocks but notable amounts of detritus were also derived from felsic, intermediate and mafic volcanic rocks, older sedimentary rocks, and ophiolitic rocks. The heavy mineral assemblage include, in order of decreasing abundance: opaque minerals (ilmenite and magnetite with minor rutile), zircon, garnet, chromian spinel, aluminum silicate mineral (probably andalusite), rutile, epidote, tourmaline and pyroxene. Zircon morphology suggests its derivation from granitic rocks. Chemistry of chromian spinel indicates that the chromian spinel grains were derived from the ultramafic cumulate member of an ophiolite suite. Garnet and ilmenite chemistry suggests their derivation from metamorphic rocks of the epidote‐amphibolite to upper amphibolite facies though other source rocks cannot be discounted entirely. Major and trace element data for the Wakino sediments suggest their derivation from igneous and/or metamorphic rocks of felsic composition. The major element compositions suggest that the type of tectonic environment was of an active continental margin. The trace element data indicate that the sediments were derived from crustal rocks with a minor contribution from mantle‐derived rocks. The trace element data further suggest that recycled sedimentary rocks are not major contributors of detritus. It appears that the granitic and metamorphic rocks of the Precambrian Ryongnam Massif in South Korea were the major contributors of detritus to the Wakino basin. A minor but significant amount of detritus was derived from the basement rocks of the Akiyoshi and Sangun Terrane. The chromian spinel appears to have been derived from a missing terrane though the ultramafic rocks in the Ogcheon Belt cannot be discounted.     

Early Cretaceous paleogeography of Korea and Southwest Japan inferred from occurrence of detrital chromian spinels

The Sindong Group was deposited in the north–south trending half‐graben Nakdong Trough, southern Korean peninsula. The occurrence of detrital chromian spinels from the Jinju Formation of the Sindong Group in the Gyeongsang Basin means that the mafic to ultramafic rocks were exposed in its provenance. The chromian spinels from the Jinju Formation are characterized by extremely low TiO₂ and Fe³⁺. Moreover, their range of Cr# is from 0.45 to 0.80 and makes a single trend with Mg#. The chemistry of chromian spinels implies that the source rocks for chromian spinels were peridotites or serpentinites, which originated in the mantle wedge. To more narrowly constrain their source rocks, the Ulsan and Andong serpentinites exposed in the Gyeongsang Basin were examined petrographically. Chromian spinels in the Andong serpentinite differ from those of the Jinju Formation and those in the Ulsan serpentinite partly resemble them. Furthermore, the Jinju chromian spinel suite is similar to the detrital chromian spinels from the Mesozoic sediments in the Circum‐Hida Tectonic zone, which includes the Nagato Tectonic zone in Southwest Japan and the Joetsu Belt in Northeast Japan. This suggests that the basement rocks, which were located along the main fault bounding the eastern edge of the Nakdong Trough, had exposures of peridotite or serpentinite. It is possible that the Nakdong Trough was directly adjacent to the Circum‐Hida Tectonic zone before the opening of the Sea of Japan (East Sea).     

Bay of Islands ophiolite suite,Newfoundland: Petrologic and geochemical characteristics with emphasis on rare earth element geochemistry

Characteristic geochemical features of the ophiolite suite from the Bay of Islands Complex have been determined by major and trace element analyses of 13 rocks. Based on elements, such as rare earth elements (REE), whose abundances are relatively immobile during alteration and metamorphism, we find that (1) the pillow lavas and diabases are relatively depleted in light REE similar to most tholeiites occurring along spreading oceanic ridges, in back-arc basins and comprising the early phases of volcanism in island arcs; (2) the gabbros, composed of cumulate plagioclase and olivine with poikilitic clinopyroxene, have REE contents consistent with formation as cumulates precipitated from magmas represented by the overlying pillow lavas and diabases; (3) as in most harzburgites from ophiolites, the Bay of Islands harzburgite and dunite have relative REE abundances inconsistent with a genetic relationship to the overlying basic rocks — this inconsistency may be primary or it may result from late-stage alteration, contamination and/or metamorphism; (4) some Bay of Islands lherzolites have major and trace element abundances expected in the mantle source of the overlying basic rocks. Overall, the geochemical features of this Bay of Islands ophiolite suite are similar to those from Troodos and Vourinos, but these data are not sufficient to distinguish between different tectonic environments such as deep ocean ridge, small ocean basin or young island arc.     

西藏南部蛇绿岩套电导率研究

大地电磁(MT)资料显示,青藏高原地壳及地幔中普遍存在着高导层.作为大陆造山带中古洋盆岩石圈残片,蛇绿岩套的电导率测量可为了解古洋盆地区地壳及地幔的电性结构提供极其有用的信息.本研究中,我们在压力为1 GPa或3 GPa下,用交流阻抗谱法测量了采自西藏南部地区的蚀变辉长岩、玄武岩、角闪橄榄岩及方辉橄榄岩四个样品的阻抗谱,并进一步得出样品的电导率,不同样品电导率与温度之间的关系满足Arrhenius关系式.在实验温度范围内,蛇绿岩套电导率的对数logσ位于-6.0~-0.5 S/m之间,且随着温度的增高,不同样品电导率增大约4~5.5个量级.样品在未脱水的情况下,低温段的活化焓变化范围在0.4~0.6 eV之间,高温段的活化焓变化范围为1.7~2.6 eV之间.同时,我们研究了样品中结构水含量及铁含量对实验电导率的影响,验证了样品电导率与铁含量之间呈正比关系.当对样品结构水含量进行归一化后,相同温度下各样品的电导率随铁含量的增加而增大,而对样品铁含量归一化后,相同温度下各样品的电导率随样品中水含量的增加而增大.将实验电导率与藏南地区大地电磁结果进行了对比,发现本研究中各样品高温段实验电导率结果均落在大地电磁结果范围内.