http://dx.doi.org/10.1016/j.gsf.2016.11.007

Lunar anorthosite is a major rock of the lunar highlands,which formed as a result of plagioclasefloatation in the lunar magma ocean(LMO).Constraints on the sufficient conditions that resulted in the formation of a thick pure anorthosite(mode of plagioclase 95 vol.%) is a key to reveal the early magmatic evolution of the terrestrial planets.To form the pure lunar anorthosite,plagioclase should have separated from the magma ocean with low crystal fraction.Crystal networks of plagioclase and mafic minerals develop when the crystal fraction in the magma(φ) is higher than ca.40-60 vol.%,which inhibit the formation of pure anorthosite.In contrast,when φ is small,the magma ocean is highly turbulent,and plagioclase is likely to become entrained in the turbulent magma rather than separated from the melt.To determine the necessary conditions in which anorthosite forms from the LMO,this study adopted the energy criterion formulated by Solomatov.The composition of melt,temperature,and pressure when plagioclase crystallizes are constrained by using MELTS/pMELTS to calculate the density and viscosity of the melt.When plagioclase starts to crystallize,the Mg~# of melt becomes 0.59 at 1291 C.The density of the melt is smaller than that of plagioclase for P 2.1 kbar(ca.50 km deep),and the critical diameter of plagioclase to separate from the melt becomes larger than the typical crystal diameter of plagioclase(1.8-3 cm).This suggests that plagioclase is likely entrained in the LMO just after the plagioclase starts to crystallize.When the Mg~# of melt becomes 0.54 at 1263 C,the density of melt becomes larger than that of plagioclase even for 0 kbar.When the Mg~# of melt decreases down to 0.46 at 1218 C,the critical diameter of plagioclase to separate from the melt becomes 1.5-2.5 cm,which is nearly equal to the typical plagioclase of the lunar anorthosite.This suggests that plagioclase could separate from the melt.One of the differences between the Earth and the Moon is the presence of water.If the terrestrial magma ocean was saturated with H_2O,plagioclase could not crystallize,and anorthosite could not form.     

Subsidence of the Miyako‐Sone submarine carbonate platform,east of Miyako‐jima Island,northwestern Pacific Ocean

Bathymetric mapping and observations of the seafloor using a remotely operated vehicle (ROV, Hyper‐Dolphin 3K) were carried out on the slopes of the Miyako‐Sone submarine platform, east of Miyako‐jima in the Ryukyu Islands, northwestern Pacific Ocean. The bathymetric map indicates that terraces are present at water depths of approximately 140 m, 330 m, 400 m, and 680 m on the northwestern slope of the platform. A number of NW–SE trending lineaments, probably faults, extend perpendicular to the axis of the Ryukyu Island Arc. Two ROV surveys were conducted at water depths ranging from 519 m (on the slope) to 121 m (shallowest part of the platform). The surveys revealed that well‐indurated carbonate rocks are exposed at terrace margins and on upper slopes, and that the lower slopes are covered with modern sediments consisting of unconsolidated, coarse‐sand‐sized bioclastic carbonates. Calcareous nannofossils from the well‐indurated carbonate rocks indicate a Middle–Late Pleistocene age, which suggests that the rocks correlate with the Quaternary reef and fore‐reef deposits of the Ryukyu Group (Ryukyu Limestone) on the Ryukyu Islands. No siliciclastic deposits corresponding to the upper Miocene–lower Pleistocene Shimajiri Group (as exposed on Okinawa‐jima and Miyako‐jima islands) were recovered during the surveys. Coeval well‐indurated carbonate rocks, all of which formed in a similar sedimentary environment, have been downthrown towards the west due to displacements on the western sides of normal faults. Subsidence of the Miyako‐Sone submarine platform was the result of large vertical displacements on such normal faults. The timing of initial subsidence cannot be tightly constrained, but the presence of the youngest limestone at progressively lower levels towards the west suggests the subsidence continued until after 0.265 Ma.     

Pressure-temperature dependent compositional variation of phlogopitic micas in upper mantle peridotites

Compositional variation of phlogopitic micas in upper mantle peridotites is reviewed. Phlogopitic micas in garnet peridotites are systematically lower in Al (or eastonite component) than those in spinel peridotites. The core of phlogopite megacryst and phenocryst of kimberlite is always lower in Al than the rim. It is apparent that Al/(Al + Si) ratio or eastonite component in phlogopitic micas in ultramafic rocks is controlled by the equilibrium pressure and temperature. In the upper mantle peridotites containing garnet or spinel, the Al/(Al + Si) ratio of phlogopitic mica decreases with increasing pressure at constant temperature. Phlogopitic mica is a potential thermo-barometer in both garnet- and spinel-peridotite facies.     

Application of laser ablation ICPMS to trace the environmental history of chum salmon Oncorhynchus keta

Trace element levels in otoliths of chum salmon Oncorhynchus keta were examined by means of laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS). A close linear relationship in the Sr:Ca ratios between EPMA (X-ray analysis with an electron microprobe) and LA-ICPMS analyses was found (p<0.0001), suggesting that the latter technique could be used to separate the marine and freshwater life phases. Mg:Ca, Cr:Ca, Zn:Ca and Ba:Ca ratios in either the core region or the oceanic growth zone of the otoliths varied among sites. These differences suggest that elemental compositions may reflect environmental variability among spawning (breeding) or habitat sites. Thus, those element ratios demonstrate the potential to be used to distinguish between fish spawning (breeding) sites and habitats for this species of salmon.     

Cause and countermeasure of long-period oscillations of moored ships and the quantification of surge and heave amplitudes

Long-period oscillations of moored ships whose periods are about 1 or 2 min cause many troubles in many ports and harbours. It is necessary to investigate these phenomena and verify their causes and countermeasures in each case because they are strongly dependent on the environment of each port and harbour. From this point of view, long-period oscillations of moored ships in the Port of Shibushi in Japan were investigated by means of wave observations, the image processing of moored ship motions using the video camera and motion-capture software and numerical simulations. From observation results, the relationship between offshore long-period waves and long-period oscillations of moored ships was recognized and surge and heave amplitudes were quantified by using wave data in order to forecast moored ship motions. Furthermore, from observation and numerical results, it was revealed that long-period waves with the peak period of 120 s from the offshore typhoon kept or exaggerated the local harbour oscillation of 60–70 s and it caused long-period oscillations of moored ships. Numerical results in case of reducing the reflection coefficient of the target berth implied that it ceased the local harbour oscillation and it would give an effective countermeasure to reduce long-period oscillations of moored ships in the Port of Shibushi.     

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

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

Unexpectedly high-PGE chromitite from the deeper mantle section of the northern Oman ophiolite and its tectonic implications

Unusually high, platinum-group element (PGE) enrichments are reported for the first time in a podiform chromitite of the northern Oman ophiolite. The chromitite contains Б.5 ppm of total PGE, being highly enriched in the IPGE subgroup (Ir, Os and Ru) and strongly depleted in the PPGE subgroup (Rh, Pt and Pd). Its platinum-group minerals (PGMs) are classified into three types arranged in order of abundance: (1) sulphides (Os-rich laurite, laurite-erlishmanite solid solution and an unnamed Ir sulphide), (2) alloys (Os-Ir alloy and Ir-Rh alloy), and (3) sulpharsenides (irarsite and hollingworthite). The high PGE concentrations are observed only in a discordant chromitite deep in the mantle section, which has high-Cr# (>0.7) spinel with an olivine matrix. All the other types of chromitite (in the Moho transition zone (MTZ) and concordant pods in the deeper mantle section) are poor in PGEs and tend to have spinels with lower Cr# (up to 0.6). This diversity of chromitite types suggests two stages of magmatic activity were responsible for the chromitite genesis, in response to a switch of tectonic setting. The first is residual from lower degree, partial melting of peridotite, which produced low-Cr#, PGE-poor chromitites at the Moho transition zone and, to a lesser extent, within the mantle, possibly beneath a fast-spreading mid-ocean ridge. The second chromitite-forming event involves higher degree partial melting, which produced high-Cr#, PGE-rich discordant chromitite in the upper mantle, possibly in a supra-subduction zone setting.     

Lower Oligocene Calc-Alkaline Spessartitic Lamprophyres from Central Iran (East of Anarak Area); an Evidence from the Eastern Branch of Neotethys Subduction-Related Mantle Enrichment

Geotectonics - The Lower Oligocene Kal-e-kafi (East of Anarak, Central Iran) lamprophyres occur as stocks and dikes, which cross-cut the Eocene volcanic and Cretaceous sedimentary rocks. The...     

Magmatic unmixing in spinel from late Precambrian concentrically-zoned mafic–ultramafic intrusions, Eastern Desert, Egypt

Spinel is widespread in the ultramafic core rocks of zoned late Precambrian mafic–ultramafic complexes from the Eastern Desert of Egypt. These complexes; Gabbro Akarem, Genina Gharbia and Abu Hamamid are Precambrian analogues of Alaskan-type complexes, they are not metamorphosed although weakly altered. Each intrusion is composed of a predotite core enveloped by pyroxenites and gabbros at the margin. Silicate mineralogy and chemistry suggest formation by crystal fractionation from a hydrous magma. Relatively high Cr₂O₃ contents are recorded in pyroxenes (up to 1.1 wt.%) and amphiboles (up to 1.4 wt.%) from the three plutons. The chrome spinel crystallized at different stages of melt evolution; as early cumulus inclusions in olivine, inclusions in pyroxenes and amphiboles and late-magmatic intercumulus phase. The intercumulus chrome spinel is homogenous with narrow-range of chemical composition, mainly Fe³⁺-rich spinel. Spinel inclusions in clinopyroxene and amphibole reveal a wide range of Al (27–44 wt.% Al₂O₃) and Mg (6–13 wt.% MgO) contents and are commonly zoned. The different chemistries of those spinels reflect various stages of melt evolution and re-equilibration with the host minerals. The early cumulus chrome spinel reveals a complex unmixing structures and compositions. Three types of unmixed spinels are recognized; crystallographically oriented, irregular and complete separation. Unmixing products are Al-rich (Type I) and Fe³⁺-rich (Type II) spinels with an extensive solid solution between the two end members. The compositions of the unmixed spinels define a miscibility gap with respect to Cr–Al–Fe³⁺, extending from the Fe³⁺–Al join towards the Cr corner. Spinel unmixing occurs in response to cooling and the increase in oxidation state. The chemistry and grain size of the initial spinel and the cooling rate control the type of unmixing and the chemistry of the final products. Causes of spinel unmixing during late-magmatic stage are analogous to those in metamorphosed complexes. The chemistry of the unmixed spinels is completely different from the initial spinel composition and is not useful in petrogenetic interpretations. Spinels from oxidized magmas are likely to re-equilibrate during cooling and are not good tools for genetic considerations.