Gonadal histology and serum vitellogenin levels of bigeye tuna Thunnus obesus from the Northern Pacific Ocean--absence of endocrine disruption bio-indicators

Endocrine disrupting chemicals such as organochlorines have been detected in a large number of marine fish. Histological observation of the gonads, measurement of serum vitellogenin (VTG) level and of liver polychlorinated biphenyl (PCB) content were performed to evaluate the reproductive health and the contamination with endocrine disruptors in bigeye tuna Thunnus obesus, collected in the northern Pacific Ocean in 1999 and 2000. Abnormalities commonly found in species affected by endocrine disruptors such as the presence of oocytes in the testis or elevated serum VTG levels were not found in any of males examined. Both males and females had only small amounts of liver PCB content. The results suggest that currently there is little if any risk of organochlorine contamination or endocrine disruption of gonadal function in bigeye tuna from the northern Pacific Ocean. However, further studies are necessary to evaluate the health status of the open sea fishery resources.     

Alkaline leaching characteristics of biogenic opal in Eocene sediments from the central Arctic Ocean: a case study in the ACEX cores

Accurate knowledge of the extent of biogenic opal preservation in marine sediment cores is important for paleoceanographic reconstructions. The alkaline leaching method is widely employed for %biogenic opal analysis due to its ease and speed. In this study, a revised method for measuring %biogenic opal in sediment from arctic coring expedition samples was suggested. The studied middle Eocene sediments from the central Arctic Ocean presented a problem in insufficiently leaching biogenic opal with a Na₂CO₃ solution. Based on XRD analysis, it was suggested that such an alkaline resistance results from slight diagenesis of biogenic opal. In order to solve this problem, an alkaline leaching method utilizing a 2 M NaOH solution was suggested for the accurate measurement of %biogenic opal in the Eocene sediments from the central Arctic. Furthermore, dissolution rates from lithogenic matter by NaOH solution were measured in order to correct the %biogenic opal values.     

The structure of monomeric and dimeric uranyl adsorption complexes on gibbsite: A combined DFT and EXAFS study

We investigated the structure of uranyl sorption complexes on gibbsite (pH 5.6-9.7) by two independent methods, density functional theory (DFT) calculations and extended X-ray absorption fine structure (EXAFS) spectroscopy at the U-L_III edge. To model the gibbsite surface with DFT, we tested two Al (hydr)oxide clusters, a dimer and a hexamer. Based on polarization, structure, and relaxation energies during geometry optimization, the hexamer cluster was found to be the more appropriate model. An additional advantage of the hexamer model is that it represents both edges and basal faces of gibbsite. The DFT calculations of (monomeric) uranyl sorption complexes show an energetic preference for the corner-sharing versus the edge-sharing configuration on gibbsite edges. The energy difference is so small, however, that possibly both surface species may coexist. In contrast to the edge sites, sorption to basal sites was energetically not favorable. EXAFS spectroscopy revealed in all investigated samples the same interatomic distances of the uranyl coordination environment (R_U-Oax ≈ 1.80 Å, R_U-Oeq ≈ 2.40 Å), and towards the gibbsite surface (R_U-O ≈ 2.87 Å, R_U-Al ≈ 3.38 Å). In addition, two U-U distances were observed, 3.92 Å at pH 9.7 and 4.30 Å at pH 5.6, both with coordination numbers of ∼1. The short U-U distance is close to that of the aqueous uranyl hydroxo dimer, UO₂(OH)₂, reported as 3.875 Å in the literature, but significantly longer than that of aqueous trimers (3.81-3.82 Å), suggesting sorption of uranyl dimers at alkaline pH. The longer U-U distance (4.30 Å) at acidic pH, however, is not in line with known aqueous uranyl polymer complexes. Based on the EXAFS findings we further refined dimeric surface complexes with DFT. We propose two structural models: in the acidic region, the observed long U-U distance can be explained with a distortion of the uranyl dimer to form both a corner-sharing and an edge-sharing linkage to neighboring Al octahedra, leading to R_U-U = 4.150 Å. In the alkaline region, a corner-sharing uranyl dimer complex is the most favorable. The U-O path at ∼2.87 Å in the EXAFS spectra arises from the oxygen atom linking two Al cations in corner-sharing arrangement. The adsorption structures obtained by DFT calculations are in good agreement with the structural parameters from EXAFS analysis: U-Al (3.394 Å), U-U (3.949 Å), and U-O (2.823 Å) for the alkaline pH model, and U-Al (3.279 Å), U-U (4.150 Å), and U-O (2.743 Å) for the acidic pH model. This work shows that by combining EXAFS and DFT, consistent structural models for uranyl sorption complexes can be obtained, which are relevant to predict the migration behavior of uranium at nuclear facilities.     

Decadal seesaw of the Central and Subtropical Mode Water formation associated with the Kuroshio Extension variability

Available Argo profiling float data from 2002 to 2011 were analyzed to examine the effect of the Kuroshio Extension (KE) current system variability on the formation of the Central Mode Water. Just north of the upstream portion of the KE at 140–152°E, formation of a lighter variety of the Central Mode Water in winter was active during the unstable period of the upstream KE in 2006–2009 and was reduced when the upstream KE was in the stable period of 2002–2005 and 2010–2011. This decadal formation variability is out of phase with that of the Subtropical Mode Water just south of the KE.     

Correlation of large displacement drained shear strength of landslide soils measured by direct shear and ring shear devices

Based on a laboratory study of drained direct shear tests of remoulded, pre-cut and polished specimens and drained ring shear tests of uncut and remoulded specimens of slip surface materials of five landslide soils, significant correlations of the mobilized shear strength parameters, cohesion (c, c _r) and internal friction angle (Φ, Φ_r), are proposed. The investigated soils consisted of the slip surface material belonging to tuffaceous clay, mudstone, loess and siltstone. Most of the previous studies on residual shear strength measured by reversal direct shear and ring shear devices have obtained significantly different results using the two devices, even when pre-cut and polished specimens were used in the direct shear device. In this study, the residual shear strength values of remoulded specimens measured by a ring shear device are shown to significantly correlate with the drained large displacement shear strength values of remoulded specimens, which were measured using pre-cut and polished specimens in a direct shear device. The correlation between the cohesion measured in the two shear devices is expressed by the linear relationship, $ {c_{\text{r}}} = 0.{7394}c - {6}.{6857} $ , while the correlation between the friction angle measured in the two devices is expressed by the linear relationship, $ {\Phi_{\text{r}}} = {1}.0{852}\Phi - {6}.0{247} $ . The proposed linear correlations for effective cohesion (c′) and effective friction angle (Φ′) have yielded significant coefficients of determination within an effective normal stress range of 30–150?kN/m².     

Using aerial photography and in situ measurements to estimate the quantity of macro-litter on beaches

This study has demonstrated a reliable method of quantifying the total mass of litter on a beach. It was conducted on Ookushi beach, Goto-Islands, Japan, and uses a combination of balloon-assisted aerial photography and in situ mass measurements. The total mass of litter over the beach was calculated to be 716 ± 259 kg. This figure was derived by multiplying the litter-covered area (calculated using balloon-assisted aerial photography) by the mass of litter per unit area. Light plastics such as polyethylene made up 55% of all plastic litter on the beach, although more work is needed to determine whether lighter plastics are transported to beaches more readily by winds and ocean currents compared with heavier plastics, or whether lighter plastics comprise a greater percentage of marine litter. Finally, the above estimates were used to calculate the total mass of metals released into coastal ecosystems via plastic litter on beaches.     

3-D internal architecture of methane hydrate-bearing turbidite channels in the eastern Nankai Trough, Japan

The reservoir architecture of methane hydrate (MH) bearing turbidite channels in the eastern Nankai Trough, offshore Japan is evaluated using a combination of 3-D seismic and well data. On the 3-D seismic section, the MH-bearing turbidite channels correspond to complex patterns of strong seismic reflectors, which show the 3-D internal architecture of the channel complex. A seismic-sequence stratigraphic analysis reveals that the channel complex can be roughly classified into three different stages of depositional sequence (upper, middle, and lower). Each depositional sequence results in a different depositional system that primarily controls the reservoir architecture of the turbidite channels. To construct a 3-D facies model, the stacking patterns of the turbidite channels are interpreted, and the reservoir heterogeneities of MH-bearing sediments are discussed. The identified channels at the upper sequence around the β1 well exhibit low-sinuosity channels consisting of various channel widths that range from tens to several hundreds of meters. Paleo-current flow directions of the turbidite channels are typically oriented along the north-northeast-to-south-southwest direction. High-amplitude patterns were identified above the channels along the north-to-south and north-northeast-to-south-southeast directions. These roughly coincide with the paleo-current flow of the turbidite channels. An interval velocity using high-density velocity analysis shows that velocity anomalies (>2000 m/s) are found on the northeastern side of the turbidite channels. The depositional stage of the northeastern side of the turbidite channels exhibits slightly older sediment stages than the depositional stages of the remaining channels. Hence, the velocity anomalies of the northeastern side of the channels are related to the different stages of sediment supply, and this may lead to the different reservoir architectures of the turbidite channels.     

Analytical laboratory comparison of major and minor constituents in an active crater lake

The crater lake water from Maly Semiachik volcano in Kamchatka was used for the international analytical laboratory comparison of major and minor elements, and hydrogen, sulfur, and oxygen isotope data. Eight institutions participated in this program, giving analytical results of 9 major and 20 minor elements mainly by using ICP-AES for cations and IC for anions. Among the major elements, Na, Mg and Si showed coefficients of variation (CV) of 10% or more, whereas B, Al, Fe, Mn had coefficients less than 7%. The CV% of the minor elements Co, Cu, P, Cr, Pb was much greater (>30%) while the V analyses agreed well (<10%). Ti, Sr, Zn, and F were intermediate (between 10 and 20 CV%). The errors observed for these constituents are inherent to the methods applied: large dilutions and spectrometric interferences. Even the major anions such as Cl (>2000 ppm) and SO₄ (>5000 ppm) gave considerable ranges (5.1 and 8.8 CV%, respectively) as did the obtained pH values (22 CV%). The measured δ¹⁸O of the water samples and δ³⁴S of sulfate are in excellent agreement but the δD values had CV% of 8. Technical recommendations are presented to improve the analytical results for these elements with significant deviations from the mean values.     

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.