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 peridotites from the Western Pacific

We review petrographical and petrological characteristics of mantle peridotite xenoliths from the Western Pacific to construct a petrologic model of the lithospheric mantle beneath the convergent plate boundary. The peridotite varies from highly depleted spinel harzburgite of low-pressure origin at the volcanic front of active arcs (Avacha of Kamchatka arc and Iraya of Luzon–Taiwan arc) to fertile spinel lherzolite of high-pressure origin at the Eurasian continental margin (from Sikhote-Alin through Korea to eastern China) through intermediate lherzolite–harzburgite at backarc side of Japan island arcs. Oxygen fugacity recorded by the peridotite xenoliths decreases from the frontal side of arc to the continental margin. The sub-arc type peridotite is expected to exist beneath the continental margin if accretion of island arc is one of the important processes for continental growth. Its absence suggests replacement by the continental lherzolite at the region of backarc to continental margin. Asthenospheric upwelling beneath the continental region, which has frequently occurred at the Western Pacific, has replaced depleted sub-cratonic peridotite with the fertile spinel lherzolite. Some of these mantle diapirs had opened backarc basins and strongly modified the lithospheric upper mantle by metasomatism and formation of Group II pyroxenites.     

Uranyl adsorption and surface speciation at the imogolite-water interface: Self-consistent spectroscopic and surface complexation models

Macro- and molecular-scale knowledge of uranyl (U(VI)) partitioning reactions with soil/sediment mineral components is important in predicting U(VI) transport processes in the vadose zone and aquifers. In this study, U(VI) reactivity and surface speciation on a poorly crystalline aluminosilicate mineral, synthetic imogolite, were investigated using batch adsorption experiments, X-ray absorption spectroscopy (XAS), and surface complexation modeling. U(VI) uptake on imogolite surfaces was greatest at pH ∼7-8 (I = 0.1 M NaNO₃ solution, suspension density = 0.4 g/L [U(VI)]_i = 0.01-30 μM, equilibration with air). Uranyl uptake decreased with increasing sodium nitrate concentration in the range from 0.02 to 0.5 M. XAS analyses show that two U(VI) inner-sphere (bidentate mononuclear coordination on outer-wall aluminol groups) and one outer-sphere surface species are present on the imogolite surface, and the distribution of the surface species is pH dependent. At pH 8.8, bis-carbonato inner-sphere and tris-carbonato outer-sphere surface species are present. At pH 7, bis- and non-carbonato inner-sphere surface species co-exist, and the fraction of bis-carbonato species increases slightly with increasing I (0.1-0.5 M). At pH 5.3, U(VI) non-carbonato bidentate mononuclear surface species predominate (69%). A triple layer surface complexation model was developed with surface species that are consistent with the XAS analyses and macroscopic adsorption data. The proton stoichiometry of surface reactions was determined from both the pH dependence of U(VI) adsorption data in pH regions of surface species predominance and from bond-valence calculations. The bis-carbonato species required a distribution of surface charge between the surface and β charge planes in order to be consistent with both the spectroscopic and macroscopic adsorption data. This research indicates that U(VI)-carbonato ternary species on poorly crystalline aluminosilicate mineral surfaces may be important in controlling U(VI) mobility in low-temperature geochemical environments over a wide pH range (∼5-9), even at the partial pressure of carbon dioxide of ambient air (p_CO2 = 10^−3.45 atm).     

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.     

Degradation of algal lipids by deep-sea benthic foraminifera: An in situ tracer experiment

We conducted an in situ feeding experiment using ¹³C-labeled unicellular algae in Sagami Bay, Japan (water depth, 1450 m), in order to understand the fate of lipid compounds in phytodetritus at the deep-sea floor. We examined the incorporation of excess ¹³C into lipid compounds extracted from bulk sediments and benthic foraminiferal cells. ¹³C-enriched fatty acids derived from ¹³C-labeled algae were exponentially degraded during 6 days of incubation in the sediment. Subsequent enrichments in ¹³C in sedimentary n-C_15, anteiso-C₁₇, and C₁₇ fatty acids indicated the microbial degradation of algal material and production of bacterial biomass in the sediment. We observed the incorporation of ¹³C-labeled algal phytol and fatty acids into foraminiferal cells. The compositions of ¹³C-labeled algal lipids in foraminiferal cells were different from those in the bulk sediments, indicating that foraminiferal feeding and digestion influenced the lipid distribution in the sediments. Furthermore, some sterols in Globobulimina affinis (e.g., 24-ethylcholesta-5,22-dien-3β-ol, 24-ethylcholest-5-en-3β-ol, and 23,24-dimethylcholesta-5,22E-dien-3β-ol) were newly produced via the modification of dietary algal sterols within 4–6 days. In addition to the effects of bacteria, feeding by benthic foraminifera can result in a significant reorganization of the composition of organic matter and influence benthic food webs and carbon cycling at the deep-sea floor.     

Geochemistry of spinel-hosted amphibole inclusions in abyssal peridotite: insight into secondary melt formation in melt–peridotite reaction

Spinel-hosted hydrous silicate mineral inclusions are often observed in dunite and troctolite as well as chromitite. Their origin has been expected as products associated with melt–peridotite reaction, based on the host rock origin. However, the systematics in mineralogical and geochemical features are not yet investigated totally. In this study, we report geochemical variations of the spinel-hosted pargasite inclusions in reacted harzburgite and olivine-rich troctolite collected from Atlantis Massif, an oceanic core complex, in the Mid-Atlantic Ridge. The studied samples are a good example to examine geochemical variations in the inclusions because the origin and geological background of the host rocks have been well constrained, such as the reaction between MORB melt and depleted residual harzburgite beneath the mid-ocean ridge spreading center. The trace-element compositions of the pargasite inclusions are characterized by not only high abundance of incompatible elements but also the LREE and HFSE enrichments. Distinctive trace-element partitioning between the pargasite inclusion and the host-rock clinopyroxene supports that the secondary melt instantaneously formed by the reaction is trapped in spinel and produces inclusion minerals. While the pargasite geochemical features can be interpreted by modal change reaction of residual harzburgite, such as combination of orthopyroxene decomposition and olivine precipitation, degree of the LREE enrichment as well as variation of HREE abundance is controlled by melt/rock ratio in the reaction. The spinel-hosted hydrous inclusion could be embedded evidence indicating melt–peridotite reaction even if reaction signatures in the host rock were hidden by other consequent reactions.     

Restoration of Exotic Terranes Along the Median Tectonic Line, Japanese Islands: Overview

This paper reviews recent progress on the geotectonic evolution of exotic Paleozoic terranes in Southwest Japan, namely the Paleo-Ryoke and Kurosegawa terranes. The Paleo-Ryoke Terrane is composed mainly of Permian granitic rocks with hornfels, mid-Cretaceous high-grade metamorphic rocks associated with granitic rocks, and Upper Cretaceous sedimentary cover. They form nappe structures on the Sambagawa metamorphic rocks. The Permian granitic rocks are correlative with granitic clasts in Permian conglomerates in the South Kitakami Terrane, whereas the mid-Cretaceous rocks are correlative with those in the Abukuma Terrane. This correlation suggests that the elements of Northeast Japan to the northeast of the Tanakura Tectonic Line were connected in between the paired metamorphic belt along the Median Tectonic Line, Southwest Japan. The Kurosegawa Terrane is composed of various Paleozoic rocks with serpentinite and occurs as disrupted bodies bounded by faults in the middle part of the Jurassic Chichibu Terrane accretionary complex. It is correlated with the South Kitakami Terrane in Northeast Japan. The constituents of both terranes are considered to have been originally distributed more closely and overlay the Jurassic accretionary terrane as nappes. The current sporadic occurrence of these terranes can possibly be attributed to the difference in erosion level and later stage depression or transtension along strike-slip faults. The constituents of both exotic terranes, especially the Ordovician granite in the Kurosegawa-South Kitakami Terrane and the Permian granite in the Paleo-Ryoke Terrane provide a significant key to reconstructing these exotic terranes by correlating them with Paleozoic granitoids in the eastern Asia continent.     

Silica enrichment of Group II xenoliths by evolved alkali basalt from Jeju Island, South Korea: implication for modification of intraplate deep-seated rocks

Group II xenoliths, corresponding to the lithology of dunite, wehrlite to olivine clinopyroxenite and olivine websterite to websterite, occur in Pleisto-Holocene alkali basalts from Jeju Island, South Korea. The large grain size (up to 5?mm), moderate mg# [=100?×?Mg/(Mg?+?Fe_total) atomic ratio] of olivine (79–82) and pyroxenes (77–83), and absence of metamorphic textural features indicate that they are cumulates of igneous origin. Based on textural features, mineral equilibria and major and trace element variations, it can be inferred that the studied xenoliths were crystallized from basaltic melts enriched in incompatible trace elements and belong to the Jeju Pleisto-Holocene magma system. They appear to have been emplaced near the present Moho, an estimated 5–8?kbars beneath Jeju Island. Consolidation of cumulates was followed by infiltration of silica-enriched metasomatic melt, producing secondary orthopyroxenes at the expense of olivine. The metasomatic agent appears to have been a silica-enriched residual melt evolved from an initially slightly silica-undersaturated alkali basalt to silica-saturated compositions by fractional crystallization under relatively high pressure conditions. The result of this study indicates that relatively young olivine-bearing cumulates could have been metasomatized by a silica-enriched melt within underplates, suggesting that silica enrichment can occur in intraplate Moho-related rocks as well as in the upper mantle of the subarc area.     

Origin of wehrlite cumulates in the Moho transition zone of the Neoproterozoic Ras Salatit ophiolite,Central Eastern Desert,Egypt: crustal wehrlites with typical mantle characteristics

Ultramafic cumulates, mainly crustal true wehrlites, were discovered and described in the mantle–crust transition zone (MTZ) and the extremely lower layered gabbro sequence of the Ras Salatit ophiolite, Central Eastern Desert, Egypt. They form either boudinaged lensoidal tabular bodies or interdigitated layers often concordant with the planolinear fabrics of the Ras Salatit ophiolite rocks. The contact between wehrlites and the host MTZ dunite or layered gabbro is razor sharp, lobate and/or sinuous, without chilled margins or any visible deformations. The Ras Salatit wehrlites are orthopyroxene-free and composed mainly of olivine and clinopyroxene. They are texturally equilibrated and show a characteristic poikilitic texture. Crystallization order of the Ras Salatit wehrlites is olivine/spinel followed by clinopyroxene with the absence of plagioclase. Olivine and clinopyroxene of the Ras Salatit wehrlites are compositionally uniform and conspicuously high in Mg#, mostly around 0.93 and 0.92, respectively. Moreover, the clinopyroxene shows low Ti and Al contents coupled with marked depletion in LILE. The calculated melt in equilibrium with clinopyroxene from the Ras Salatit wehrlites is largely similar to lavas from the Izu-Bonin forearc. Given the above characteristics, the Ras Salatit wehrlites were produced by crystal accumulation from a hydrous depleted basaltic/tholeiitic melt corresponding to temperatures between 1,000 and 1,100°C at the oceanic crustal pressure (~2 kbar). The involved hydrous tholeiitic melt has been probably formed by fluid-assisted partial melting of a refractory mantle source (similar to the underlying harzburgites) in a somewhat shallow sub-arc environment.