Chromitite and peridotite from Rayat, northeastern Iraq, as fragments of a Tethyan ophiolite

Ophiolitic rocks (chromitites and serpentinized peridotites) were petrologically examined in detail for the first time from Rayat, in the Iraqi part of the Zagros thrust zone, an ophiolitic belt. Almost all the primary silicates have been altered out, but chromian spinel has survived from alteration and gives information about the primary petrological characteristics. The protolith of the serpentinite was clinopyroxene-free harzburgite with chromian spinel of intermediate Cr# (= Cr/[Cr + Al] atomic ratio) of 0.5 to 0.6. The harzburgite with that signature is the most common in the mantle section of the Tethyan ophiolites such as the Oman ophiolite, and is the most suitable host for chromitite genesis. Except for one sample, which has Cr# = 0.6 for spinel, the Cr# of spinel is high, around 0.7, in chromitite. The variation in Cr# of spinel in chromitite observed here has been also reported in the Oman ophiolite. The peridotite with chromitite pods exposed at Rayat was derived from an ophiolite similar in petrological character to the Oman ophiolite, one of the typical Tethyan ophiolites (fragments of Tethyan oceanic lithosphere). This result is consistent with the previous interpretation based on geological analysis.     

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.     

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.     

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.     

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.     

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.     

Petrological feature of spinel lherzolite xenolith from Oki-Dogo Island: An implication for variety of the upper mantle peridotite beneath southwestern Japan

Abstract   Spinel lherzolite is a minor component of the deep-seated xenolith suite in the Oki-Dogo alkaline basalts, whereas other types of ultramafic (e.g. pyroxenite and dunite) and mafic (e.g. granulite and gabbro) xenoliths are abundant. All spinel lherzolite xenoliths have spinel with a low Cr number (Cr#; < 0.26). They are anhydrous and are free of modal metasomatism. Their mineral assemblages and microtextures, combined with the high NiO content in olivine, suggest that they are of residual origin. But the Mg numbers of silicate minerals are lower (e.g. down to Fo₈₆) in some spinel lherzolites than in typical upper mantle residual peridotites. The clinopyroxene in the spinel lherzolite shows U-shaped chondrite-normalized rare-earth element (REE) patterns. The abundance of Fe-rich ultramafic and mafic cumulate xenoliths in Oki-Dogo alkali basalts suggests that the later formation of those Fe-rich cumulates from alkaline magma was the cause of Fe- and light REE (LREE)-enrichment in residual peridotite. The similar REE patterns are observed in spinel peridotite xenoliths from Kurose and also in those from the South-west Japan arc, which are non-metasomatized in terms of major-element chemistry (e.g. Fo > 89), and are rarely associated with Fe-rich cumulus mafic and ultramafic xenoliths. This indicates that the LREE-enrichment in mantle rocks has been more prominent and prevalent than Fe and other major-element enrichment during the metasomatism.     

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.     

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).     

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.     

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.     

Temporal variation in primary magma compositions in the northeast Japan Arc

Abstract A remarkable temporal variation in primary magma compositions has been found in the Northeast Japan arc. The trench-side magmas have become more enriched in FeO* and the backarc-side magmas have become more depleted in FeO* while retaining almost constant SiO, levels for the last ∼20 million years. In order to understand the origin of the temporal variation, FeO* and SiO, contents in partial melts are modeled for an adiabatically-rising mantle as a function of potential temperature and original composition of the mantle material. The result demonstrates that the primary magmas that are more depleted in FeO* were derived from the mantle materials either at lower potential temperatures or with compositions more depleted in basaltic components. A possible mechanism for the inferred primary magma variability is the change in depth intervals with time of magma production in a compositionally-layered mantle wedge; greater degrees of depletion at a greater depth is reconciled with a probable thermal regime in the mantle wedge.     

Spinels in Mid-Atlantic Ridge basalts: Chemistry and occurrence

Three groups of spinels have been identified in dredged basalts from the Mid-Atlantic Ridge in the Azores region (30–40°N): (1) magnesiochromites with 0.4–0.5 Cr/(Cr + Al) are most common and characteristic of olivine tholeiites of the region; (2) titaniferous magnesiochromites are found in an olivine basalt with alkali affinities, of local occurrence and evolved in relatively high fugacity of oxygen; (3) chromian spinels with 0.23 Cr/(Cr + Al) occur in unusual high-Al picrites of local occurrence and possible high-pressure origin. Spinels are restricted in occurrence to the least fractionated lavas, with FeO^*/FeO^* + MgO ratio less than 0.575 and with Cr content greater than 350 ppm. A close relationship between Al content of liquidus spinel and Al content of magma has been observed for basaltic types. High-Al spinels deviating from this relationship, such as those found in picritic lavas from the Mid-Atlantic Ridge, may have crystallized at high pressure. The use of spinels as geobarometers in magmas of a restricted compositional range seems a promising prospect. There is no evidence of systematic variation in spinel chemistry of occurrence along the Mid-Atlantic Ridge, such as could be related to different mantle sources of the basalts, plume versus non-plume or binary mantle mixing.     

Petrology of arc volcanic rocks and their origin by mantle diapirs

Calc-alkalic chemical trends characteristic of arc volcanic rocks mainly result from three mechanisms which act additively: (1) fractional crystallization involving separation of titanomagnetite; (2) selective concentration of plagioclase phenocrysts and selective depletion of titanomagnetite phenocryst compared with the actually fractionated proportion; and (3) mixing of magmas on continuous fractionation trends. The association of calc-alkalic and tholeiitic trends in a single composite volcano may not represent different fractional crystallization processes or different chemistries of primary magmas, but the calc-alkalic chemical trend can be considered as a mixing trend resulting from mixing of various magmas on associated tholeiitic chemical trends. Chemical variations of most arc volcanic rocks, including calc-alkalic ones, can accordingly be essentially accounted for by the low-pressure fractional crystallization of phenocrystic phases from primary basaltic magmas.Crystallization sequences of arc magmas which are strongly dependent on water content in magmas are deduced from the phenocryst assemblages. The crystallization sequence changes laterally across-arc, suggesting increasing water contents in magmas toward the back-arc side, as is also seen for other incompatible elements such as K and Rb. Systematic differences in the characteristic crystallization sequence are also observed among arcs, roughly correlating with the crustal thickness. Water content in magma, like other incompatible elements, tends to increase with increasing crustal thickness. The variation of incompatible elements including water roughly represents that of the degree of partial melting of the upper mantle, which is broadly controlled by the crustal thickness.The variation of water content indicates that arc magmas are not saturated with water during differentiation to late differentiates such as dacite or rhyolite. This strongly constrains the maximum water contents in primary basaltic magma, at most 2.5 wt.%. This value suggests that magma generation beneath arcs is dependent on dry solidus of peridotite. Diapiric uprise of the hot deeper mantle and associated adiabatic decompression would be necessary for mantle peridotite to attain the temperature as high as dry solidus. Diapirs that begin to rise from the subduction zone may stop at or near the crust-mantle boundary because of the surrounding density change, and their degree of partial melting is roughly controlled by their stopped depth assuming their similar temperature. Across-arc variation is also explained by the stopped depth of diapirs, but is not controlled by crustal thickness.     

Sr–Nd isotope ratios of gabbroic and dioritic rocks in a Cretaceous-Paleogene granite terrain, Southwest Japan

Abstract Whole‐rock chemical and Sr and Nd isotope data are presented for gabbroic and dioritic rocks from a Cretaceous‐Paleogene granitic terrain in Southwest Japan. Age data indicate that they were emplaced in the late Cretaceous during the early stages of a voluminous intermediate‐felsic magmatic episode in Southwest Japan. Although these gabbroic and dioritic rocks have similar major and trace element chemistry, they show regional variations in terms of initial Sr and Nd isotope ratios. Samples from the South Zone have high initial ⁸⁷Sr/⁸⁶Sr (0.7063–0.7076) and low initial Nd isotope ratios (?_Nd, ?2.5 to ?5.3); whereas those from the North Zone have lower initial ⁸⁷Sr/⁸⁶Sr (usually less than 0.7060) and higher Nd isotope ratios (?_Nd, ?0.8 to + 3.3). Regional variations in Sr and Nd isotope ratios are similar to those observed in granitic rocks, although gabbroic and dioritic rocks tend to have slightly lower Sr and higher Nd isotope ratios than granitic rocks in the respective zones. Limited variations in Sr and Nd isotope ratios among samples from individual zones may be attributed partly to a combination of upper crustal contamination and heterogeneity of the magma source. Contamination of magmas by upper crustal material cannot, however, explain the observed Sr and Nd isotope variations between samples from the North and South Zones. Between‐zone variations would reflect geochemical difference in magma sources. The gabbroic and dioritic rocks are enriched in large ion lithophile elements (LILE) and depleted in high field strength elements (HFSE), showing similar normal‐type mid‐ocean ridge basalt (N‐MORB) normalized patterns to arc magmas. Geochronological and isotopic data may suggest that some gabbroic and dioritic rocks are genetically related to high magnesian andesite. Alternatively, mantle‐derived mafic or intermediate rocks which were underplated beneath the crust may be also plausible sources for gabbroic and dioritic rocks. The magma sources (the mantle wedge and lower crust) were isotopically more enriched beneath the South Zone than the North Zone during the Cretaceous‐Paleogene. Sr and Nd isotope ratios of the lower crustal source of the granitic rocks was isotopically affected by mantle‐derived magmas, resulting in similar initial Sr and Nd isotope ratios for gabbroic, dioritic and granitic rocks in each zone.     

Role of water in the origin of podiform chromitite deposits

We report experiments in basalt oversaturated with water to duplicate the nodular ore textures of podiform chromitite ores. In immiscible basalt-water systems saturated with olivine and chromite, olivine will reside in the melt while chromite will collect in the fluid phase. Fractionation is physical and is driven by differential wetting properties of melt and fluid against silicate and oxide surfaces. There is no need to suppress olivine from the liquidus of a primitive basaltic melt as suggested by Irvine [Irvine, T.N., Geology 5 (1977) 273-277], to achieve chromite accumulations as observed in natural podiform ore deposits. The results imply that podiform chromitite ores will form where a primitive olivine-chromite-saturated mantle melt is sufficiently water-rich to exsolve a fluid phase during passage through the uppermost mantle. The most likely geodynamic environment for podiform chromite mineralization to take place is a supra-subduction zone setting.     

Evidence for high-Ca boninite magmatism from Paleogene primitive low-K tholeiite, Mukoojima, Hahajima Island group, southern Bonin (Ogasawara) forearc, Japan

Abstract   High-Ca boninitic inclusions are found in primitive low-K tholeiite from Mukoojima (Mukoo-Jima), an islet in the Hahajima Island group, Bonin (Ogasawara) forearc, Japan. While Chichijima Island group, 50 km north of Hahajima Island group, is well known as a type locality of boninite, there has been no report of boninitic rocks from the Hahajima Island group. The high-Ca boninitic inclusions are aphanitic and contain olivine, Ca-rich clinopyroxene, plagioclase, chromian spinel, opaque minerals and dark brown glass. The mode of occurrence of the inclusions and host tholeiite under the microscope indicates mingling of these two magmas, suggesting intimate association in space and time of the boninite and primitive tholeiite magmas around the Hahajima Island group in Paleogene time. Primitive compositions and slightly different Sr and Nd isotopic ratios suggest that these two magmas are derived from two distinct mantle sources. These two mantle sources were present at the same time around the Hahajima Island group, southern Bonin forearc. The source of the high-Ca boninite was higher in water content and/or shallower in depth compared to that of the primitive tholeiite.     

Middle Miocene to Quaternary primary basalt and high magnesian andesite magmas of North Hokkaido, Japan: Source mantle characteristics and degrees of partial melting

Abstract   Middle Miocene to Quaternary primitive basalts and high magnesian andesite (HMA) in North Hokkaido resulted from three periods of intense volcanism; early-stage (12–10 Ma), middle-stage (9–7 Ma) and late-stage (3–0 Ma). Based on the chemical compositions of olivines and chromian spinels and bulk chemistry of the primitive rocks, we examined depths of segregation of the calculated primary magmas and the degrees of partial melting of the source mantle. In the context of asthenospheric mantle upwelling, petrological data from the present study can be accounted for by the secular change in the depth of magma segregation from the upwelled asthenospheric mantle, which is composed of fertile peridotite. Thus, the early-stage primary magmas were generated by higher degrees of partial melting of the shallower part of hot asthenospheric mantle, whereas the middle- and late-stage primary magmas resulted from lower degrees of partial melting of a deeper part of the asthenospheric mantle. The early-stage HMA magma was generated by partial melting of the remnant subcontinental lithospheric mantle composed of refractory peridotite. This melting might have resulted from an increased geothermal gradient caused by upwelling of hot asthenosphere.     

Source depletion and extent of melting in the Tongan sub-arc mantle

The fluid immobile High Field Strength Elements (HFSE) Nb and Ta can be used to distinguish between the effects of variable extents of melting and prior source depletion of the Tongan sub-arc mantle. Melting of spinel lherzolite beneath the Lau Basin back-arc spreading centres has the ability to fractionate Nb from Ta due to the greater compatibility of the latter in clinopyroxene. The identified spatial variation in plate velocities and separation of melt extraction zones, combined with extremely depleted lavas make Tonga an ideal setting in which to test models for arc melt generation and the role of back-arc magmatism.We present new data acquired by laser ablation-ICPMS of fused sample glasses produced without the use of a melt fluxing agent. The results show an arc trend towards strongly sub-chondritic Nb/Ta (< 17) with values as low as 7.2. Melting models show that large degree melts of depleted MORB mantle fail to reproduce the observed Nb/Ta. Alternatively, incorporation of residual back-arc mantle that has undergone less than 1% melting into the sub-arc melting regime reproduces arc values. However, the extent of partial melting required to produce the composition of the Lau Basin back-arc basalts averages 7%. This apparent discrepancy can be explained if only the lowermost 4 km of the residua from the mantle melt column beneath the back-arc is added to the source of arc magmas. We have identified that the degree of arc/back-arc coupling displayed in the rock record provides an index of the depth of hydrous melting beneath the arc. In this case, this would imply a depth of ~ 75 km for generation of arc magmas, indicating that hydrous melting in the mantle wedge is triggered by the breakdown of hydrous phases in the subducting slab.     

Mid-ocean ridge popping rocks: implications for degassing at ridge crests

The vesicle size distribution (VSD) and rare gas abundances in popping rocks from 14°N on the Mid-Atlantic Ridge provide constraints on the behavior of volatiles during ridge crest volcanism. These popping rocks, which contain 16–18 volume percent vesicles, are rare mid-ocean ridge basalt (MORB) magmas which appear to have retained much of their volatile inventory. The logarithm of vesicle population density displays the same linear correlation with decreasing size in two of the samples studied. This implies that continuous and simultaneous nucleation and bubble growth have occurred during magma ascent, with no significant perturbations due to accumulation, coalescence or loss of bubbles. In contrast, most MORB magmas display low vesicularities and we suggest that they have suffered some degree of pre-eruptive vesicle loss. We tentatively propose that large vesicles are produced by coalescence when MORB melt is at rest in chambers and conduits, and may be lost during early gas-rich episodes. Most MORB would represent residual liquids which erupt after vesicle loss has occurred, whereas popping rocks would represent a rare case where physical sorting of vesicles from melt did not occur, because storage in a magma chamber did not occur.The rare gas concentrations in the studied popping rocks are the highest yet measured in glassy ridge basalts ([He] > 50 μccSTP/g). The rare gas abundance pattern of these popping rocks probably resembles the pattern for non-vesiculated MORB magma and potentially reflects that of the depleted mantle source. This pattern is similar to the “mean MORB” pattern (computed from MORB glasses with⁴⁰Ar/³⁶Ar > 10,000) although a higher enrichment in He (and possibly Ne) compared to the heavier rare gases is observed in MORB. The overall similarity in abundance patterns for MORB and popping rocks indicates that vesiculation and vesicle loss do not fractionate the ArKrXe relative abundances from those in non-vesiculated magma, and that the modern flux ratios of these gases at ridges are similar to their elemental ratios in the depleted mantle. The degassing flux of He at ridge crests estimated from the MORB He deficit relative to popping rocks is comparable to the flux derived from the³He budget for the abyssal ocean. This suggests that degassing at ridges may be strongly influenced by the dynamics and style of submarine volcanism.