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.     

Effect of canopy openness and meteorological factors on spatial variability of throughfall isotopic composition in a Japanese cypress plantation

Spatial variability of throughfall (TF) isotopic composition, used as tracer input, influences isotope hydrological applications in forested watersheds. Notwithstanding, identification of the dominant canopy factors and processes that affect the patterns of TF isotopic variability remains ambiguous. Here, we examined the spatio‐temporal variability of TF isotopic composition in a Japanese cypress plantation, in which intensive strip thinning was performed and investigated whether canopy structure at a fine resolution of canopy effect analysis is related to TF isotopic composition and how this is affected by meteorological factors. Canopy openness, as an index of canopy structure, was calculated from hemispherical photographs at different zenith angles. TF samples were collected in a 10 × 10 m experimental plot in both pre‐thinning (from July to November 2010) and post‐thinning (from May 2012 to March 2013) periods. Our results show that thinning resulted in a smaller alteration of input δ¹⁸O of gross precipitation, whereas the changes in deuterium excess varied in both directions. Despite the temporal stability of spatial patterns in TF amount, the spatial variability of TF isotopic composition was not temporally stable in both pre‐ and post‐thinning periods. Additionally, after thinning, the isotopic composition of TF was best related to canopy openness calculated at the zenith angle of 7°, exhibiting three different relationships, that is, significantly negative, significantly positive, and nonsignificant. Changes in meteorological factors (wind speed, rainfall intensity, and temperature) were found to affect the relationships between TF δ¹⁸O and canopy openness. The observed shifts in the relationships reveal different dominant factors (partial evaporation and the selection), and canopy water flowpaths control such differences. This study provides useful insights into the spatial variability of TF isotopic composition and improves our understanding of the physical processes of interception through canopy passage.     

Longitudinal variability of the equatorial counter electrojet during the solar cycle 24

Studia Geophysica et Geodaetica - Ground and space-based geomagnetic data were used in the investigation of the longitudinal, seasonal and lunar phase dependence of the equatorial counter...     

The effect of refreezing on the isotopic composition of melting snowpack

The isotopic composition of solid and liquid portions of natural melting snowpack is investigated in detail by the separating of liquid water from snow grains at different depths of the snowpack. The slope of the δD–δ¹⁸O line for the liquid phase is found to be lower than for the solid phase. This is proved to be due to the isotopic fractionation occurring in the melt–freeze mass exchange within the snowpack. Melting of the snowpack has no clear impact on the δD–δ¹⁸O line for the solid phase, but the slope of the δD–δ¹⁸O line for the liquid shows an overall slight decrease in the melting period. When the snowpack is refrozen, the refreezing process would inevitably cause the slope of the solid phase to decrease because of the discrepancy between the slopes of the two phases. Thus the slope of the solid would become lower and lower as the diurnal melt–freeze episodes cycle throughout the melting season. This effect is then demonstrated by looking into the isotopic composition changes of glacier firn. The extent of the effect depends on the snowpack properties and environmental conditions. The slope changes also result in a decreasing trend in deuterium excess. Copyright © 2007 John Wiley & Sons, Ltd.     

Experimental study on static and impact strength of sintered agglomerates

Porous internal structure is common among small bodies in the planetary systems and possible range of porosity, strength, and scale of in-homogeneity is wide. Icy agglomerates, such as icy dust aggregates in the proto-planetary disks or icy re-accumulated bodies of fragments from impact disruption beyond snow-line would have stronger bulk strength once the component particles physically connect each other due to sintering.In this study, in order to get better understanding of impact disruption process of such bodies, we first investigated the critical tensile (normal) and bending (tangential) forces to break a single neck, the connected part of the sintered particles, using sintered dimer of macro glass particles of ∼5 mm in diameter. We found that the critical tensile force is proportional to the cross-section of the neck when the neck grows sufficiently larger than the surface roughness of the original particles. We also found that smaller force is required to break a neck when the force is applied tangentially to the neck than normally applied. Then we measured the bulk tensile strength of sintered glass agglomerates consisting of 90 particles and showed that the average tensile stress to break a neck of agglomerates in static loading is consistent with the measured value for dimers.Impact experiments with velocity from 40 to 280 m/s were performed for the sintered agglomerates with ∼40% porosity, of two different bulk tensile strengths. The size ratio of the beads to the target was 0.19. The energy density required to catastrophically break the agglomerate was shown to be much less than those required for previously investigated sintered glass beads targets with ∼40% porosity, of which the size of component bead is 10⁻² times smaller and the size ratio of the bead to target is also ∼10⁻² times smaller than the agglomerates in this study. This is probably due to much smaller number of necks for the stress wave to travel through the agglomerates and therefore the energy dissipation at the necks is minimal. Also, the much larger fraction of the surface particles enables the particles to move more freely and thus be broken more easily. The catastrophic disruption of the agglomerates is shown to occur when the projectile kinetic energy is a few times of the total energy to break all of the necks of the agglomerates. The result implies that finer fragments from sintered agglomerates may have smaller catastrophic disruption energy threshold for shattering than other larger fragments with similar porosity and bulk tensile strength but much larger number of constituent particles. If this is the case, size-dependence of (smaller is weaker) is opposite to those usually considered for the bodies in the strength regime.     

Denaturing gradient gel electrophoresis shows that bacterial communities change with mid-ocean ballast water exchange

Ships carry ballast water for better stability and to control trim. However, the discharge of ballast water near ports is known to transport invasive species from one coastal area to another. The exchange of ballast water on the high seas is supposed to reduce such invasions of exotic species. In this study, we used denaturing gradient gel electrophoresis (DGGE) to analyze the composition of the bacterial community in ballast water before and after such a mid-ocean exchange, and we also measured total bacterial counts. Our findings confirmed that the ballast water was replaced by the mid-ocean exchange, as indicated by the marked change in the composition of the bacterial community. There was also a significant decrease in bacterial abundance after the mid-ocean exchange. Finally, our findings support the incubation hypothesis, because the composition of the bacterial communities changed over time within the same ballast water.     

A petrological and geochemical study on time-series samples from Klyuchevskoy volcano,Kamchatka arc

To understand the generation and evolution of mafic magmas from Klyuchevskoy volcano in the Kamchatka arc, which is one of the most active arc volcanoes on Earth, a petrological and geochemical study was carried out on time-series samples from the volcano. The eruptive products show significant variations in their whole-rock compositions (52.0–55.5 wt.% SiO₂), and they have been divided into high-Mg basalts and high-Al andesites. In the high-Mg basalts, lower-K and higher-K primitive samples (>9 wt.% MgO) are present, and their petrological features indicate that they may represent primary or near-primary magmas. Slab-derived fluids that induced generation of the lower-K basaltic magmas were less enriched in melt component than those associated with the higher-K basaltic magmas, and the fluids are likely to have been released from the subducting slab at shallower levels for the lower-K basaltic magmas than for higher-K basaltic magmas. Analyses using multicomponent thermodynamics indicates that the lower-K primary magma was generated by ~13% melting of a source mantle with ~0.7 wt.% H₂O at 1245–1260?°C and ~1.9 GPa. During most of the evolution of the volcano, the lower-K basaltic magmas were dominant; the higher-K primitive magma first appeared in AD 1932. In AD 1937–1938, both the lower-K and higher-K primitive magmas erupted, which implies that the two types of primary magmas were present simultaneously and independently beneath the volcano. The higher-K basaltic magmas evolved progressively into high-Al andesite magmas in a magma chamber in the middle crust from AD 1932 to ~AD 1960. Since then, relatively primitive magma has been injected continuously into the magma chamber, which has resulted in the systematic increase of the MgO contents of erupted materials with ages from ~AD 1960 to present.     

Mineralogy and Isotope Geochemistry of Active Submarine Hydrothermal Field at Suiyo Seamount, Izu–Bonin Arc, West Pacific Ocean

This report presents mineralogical, geochemical and isotopic data on samples obtained using the Benthic Multi‐coring System (BMS) to drill a submarine hydrothermal deposit developed in a caldera on the summit of the Suiyo Seamount in the Izu–Bonin Island Arc, south of Japan. This deposit is regarded as the first example of Kuroko‐type sulfide mineralization on a volcano at the volcanic front of an island arc. The mineralization and hydrothermal alteration below the 300 × 150‐m area of active venting was investigated to depths of 2–9 m below the sea floor. Drilling beneath the area of active venting recovered a sequence of altered volcanic rocks (dacite lavas, pyroclastic rocks of dacite–rhyolite compositions and pumice) associated with sulfide veining and patches/veins of anhydrite. No massive sulfide was found, however, and the subsea‐floor mineralization to 10 m depth is dominated by anhydrite and clay minerals with some sulfides. Sulfide‐bearing samples contained high Au (up to 42 ppm), Ag (up to 263 ppm), As (up to 1550 ppm), Hg (up to 55 ppm), Sb (up to 772 ppm), and Se (up to 24 ppm). Electron probe microanalyzer indicated that realgar, orpiment, and mimetite were major As‐bearing minerals. The sulfides were also characterized by high Zn (>10%) compared to Cu (<6.3%) and Pb (<0.6%). The δ²⁰²Hg/¹⁹⁸Hg, δ²⁰²Hg/¹⁹⁹Hg and δ²⁰²Hg/²⁰⁰Hg of the sulfide‐bearing dacite samples and a sulfide chimney decreased with increasing Hg/Zn concentration ratio. The variation of the δ²⁰²Hg/¹⁹⁸Hg ranged from ?2.8 to +0.5‰ to relative to S‐HG02027. The large range of these δ²⁰²Hg/¹⁹⁸Hg was greater than might be expected for such a heavy element and may be due to a predominance of kinetic effects. The variation of δ²⁰²Hg/¹⁹⁸Hg of sulfide‐bearing dacite samples suggested that light Hg isotope in the vapor mixed with oxygenated seawater near sea floor during mineralization. Lead isotope ratios of the sulfide were very similar to those of the dacite lava, suggesting that lead is of magmatic origin. The ⁸⁷Sr/⁸⁶Sr ratio (0.70872) of anhydrite was different from that of the dacite lava, and suggests an Sr derivation predominantly from seawater. Hydrothermal alteration of the dacite in the Suiyo hydrothermal field was characterized by Fe‐sulfides, anhydrite, barite, montmorillonite, chlorite/montmorillonite mixed‐layer minerals, mica, and chlorite with little or no feldspar or cristobalite. Hydrothermal clay minerals changed with depth from montmorillonite to chlorite/montmorillonite mixed‐layer minerals to chlorite and mica. Hydrogen isotope ratios of chlorite/montmorillonite and mixed‐layer, mica‐chlorite composites obtained below the active venting sites ranged from ?49 to ?24‰, suggesting seawater as the dominant fluid causing alteration. Oxygen isotope ratios of anhydrite ranged from 9.2 to 10.4‰ and anhydrite formation temperatures were calculated to be 188–207°C. Oxygen isotope ratios ranged from +5.2 to +9.2‰ for montmorillonite, +3.2 to +4.5‰ for chlorite/montmorillonite mixed‐layer minerals, and +2.8 to +3.8‰ in mixtures of chlorite and mica. The formation temperatures of montmorillonite and of the chlorite–mica mixture were 160–250°C and 230–270°C, respectively. The isotope temperatures for clay minerals (220–270°C) and anhydrite (188°C) were significantly lower than the borehole temperature (308.3°C) measured just after the drilling, suggesting that temperature at this site is now higher than when clay minerals and anhydrite were formed.     

Mechanisms controlling the seasonal mixed-layer temperature and salinity of the Indonesian seas

We examine the seasonal mixed-layer temperature (MLT) and salinity (MLS) budgets in the Banda–Arafura Seas region (120–138° E, 8–3° S) using an ECCO ocean-state estimation product. MLT in these seas is relatively high during November–May (austral spring through fall) and relatively low during June–September (austral winter and the period associated with the Asian summer monsoon). Surface heat flux makes the largest contribution to the seasonal MLT tendency, with significant reinforcement by subsurface processes, especially turbulent vertical mixing. Temperature declines (the MLT tendency is negative) in May–August when seasonal insolation is smallest and local winds are strong due to the southeast monsoon, which causes surface heat loss and cooling by vertical processes. In particular, Ekman suction induced by local wind stress curl raises the thermocline in the Arafura Sea, bringing cooler subsurface water closer to the base of the mixed layer where it is subsequently incorporated into the mixed layer through turbulent vertical mixing; this has a cooling effect. The MLT budget also has a small, but non-negligible, semi-annual component since insolation increases and winds weaken during the spring and fall monsoon transitions near the equator. This causes warming via solar heating, reduced surface heat loss, and weakened turbulent mixing compared to austral winter and, to a lesser extent, compared to austral summer. Seasonal MLS is dominated by ocean processes rather than by local freshwater flux. The contributions by horizontal advection and subsurface processes have comparable magnitudes. The results suggest that ocean dynamics play a significant part in determining both seasonal MLT and MLS in the region, such that coupled model studies of the region should use a full ocean model rather than a slab ocean mixed-layer model.