Relationship between trace elements and depositional environments in shallow sediments: a case study from Southern Kanto Plain,Central Japan

Underground developments such as subways and shopping facilities have been increasing in number and magnitude in the relatively shallow subsurface of many urban areas where the earth materials commonly are composed of marine sediments. Marine sediments can contain significant amounts of toxic trace elements such as arsenic, boron, and lead. Changes in the subsurface environment caused by excavation and construction in underground developments could potentially cause these toxic elements to be dissolved into pore water of the sediments, which might lead to groundwater pollution. The purpose of this study is to investigate correlations among chemical properties of marine sediments, such as pH and electrical conductivity (EC), concentrations of toxic trace elements, and stratigraphic characteristics of the sediments. We selected three sites with different stratigraphic settings in the southern Kanto Plain around the Tokyo Metropolis. We collected core samples from shallow strata at a site in the Arakawa Lowland, southern Saitama, and at two sites in the Musashino Upland, Middle Tokyo. All sites have both marine and non-marine sediments up to 50–60 m in thickness. We determined trace element concentrations in the pore water, pH, EC, and loss on ignition. The results show that (1) the marine sediments tend to have low pH, high EC, and high sulfur concentration compared to the non-marine sediments (2) the concentration of most of the soluble heavy metals vary depending on the concentration of sulfate, the pH, and the formation processes of the strata, (3) the arsenic concentration is not related to sulfur concentration but apparently to Fe and Al concentrations, (4) the boron concentration is not related to any other properties implying that the boron level is independent of and cannot be predicted by common chemical properties, and (5) for all three sites, concentrations of most of the trace elements, EC, pH, and sulfate concentration were correlated with each other. This study shows that the concentration and potential mobilization of many toxic trace elements in marine sediments could be predicted by easily measurable pore water chemical properties such as pH and EC. This could be useful for predicting and avoiding the risk of groundwater pollution during underground development projects.     

Effect of diffuse recharge and wastewater on groundwater contamination in Douala,Cameroon

High water demand for domestic use in Douala with over 3 million inhabitants is met mainly by shallow groundwater. Field measurements and water sampling in January 2015 were carried out to examine the major controls on the groundwater composition and spatial view of ions in the water, timing of recharge and link between the recharge process and quality of the water. Fifty-two water samples were analysed for major ions and stable hydrogen and oxygen isotopes. Low pH values (3.61–6.92) in the groundwater indicated an acidic aquifer; thus, prone to acidification. The dominant water type was Na–Cl. Nitrate, which exceeded the WHO guide value of 50 mg/l in 22% of the groundwater, poses a health problem. Mass ratios of Cl^?/Br^? in the water ranged from 54 to 3249 and scattered mostly along the mixing lines between dilute waters, septic-tank effluent and domestic sewage. A majority of the samples, especially the high NO₃ ^? shallow wells, clustered around the septic-tank effluent-end-member indicating high contamination by seepage from pit latrines; hence, vulnerable to pollution. Stable isotopes in the groundwater indicated its meteoric origin and rapid infiltration after rainfall. The δ¹⁸O values showed narrow ranges and overlaps in rivers, springs, open wells and boreholes. These observations depict hydraulic connectivity, good water mixing and a homogeneous aquifer system mainly receiving local direct uniform areal recharge from rainfall. The rapid and diffused recharge favours the leaching of effluent from the pit toilets into the aquifer; hence, the high NO₃ ^? and Cl^? in shallow wells. Silicate weathering, ion exchange and leaching of waste from pit toilets are the dominant controls on the groundwater chemistry. Drilling of deep boreholes is highly recommended for good-quality water supply. However, due the hydraulic connection to the shallow aquifer, geochemical modelling of future effects of such an exploitation of the deeper aquifer should support groundwater management and be ahead of the field actions.     

Mineral classification from quantitative X-ray maps using neural network: Application to volcanic rocks

We developed a mineral classification technique of electron probe microanalyzer (EPMA) maps in order to reveal the mineral textures and compositions of volcanic rocks. In the case of lithologies such as basalt that include several kinds of minerals, X-ray intensities of several elements derived from EPMA must be considered simultaneously to determine the mineral map. In this research, we used a Kohonen self-organizing map (SOM) to classify minerals in the thin-sections from several X-ray intensity maps. The SOM is a type of artificial neural network that is trained using unsupervised training to produce a two-dimensional representation of multi-dimensional input data. The classified mineral maps of in situ oceanic basalts of the Juan de Fuca Plate allowed us to quantify mineralogical and textural differences among the marginal and central parts of the pillow basalts and the massive flow basalt. One advantage of mineral classification using a SOM is that relatively many minerals can be estimated from limited input elements. By applying our method to altered basalt which contains multiple minerals, we successfully classify eight minerals in thin-section.     

Production and transport of long-chain alkenones and alkyl alkenoates in a sea water column in the northwestern Pacific off central Japan

Sinking particles collected from year-long time-series sediment traps at 1674, 4180, 5687 and 8688 m depths, the underlying bottom sediment at 9200 m depth, and suspended particles from surface and subsurface waters in the northwestern North Pacific off Japan were analyzed for long-chain alkenones and alkyl alkenoates (A&A) which are derived mainly from Gephyrocapsacean algae, especially Emiliania huxleyi and Gephyrocapsa oceanica. Alkenone temperature records in sediment trap samples at 1674 m were almost similar to observed sea surface temperatures (SST) with a time delay of one half to one full month. However, alkenone temperatures in trap samples were about slightly lower than measured SST in late spring to early fall. The lowering might be caused by formation of the seasonal thermocline. Nevertheless, these temperature drops observed in trap samples were smaller than those actually observed in a subsurface layer off central Japan. Vertical profiles of A&A concentrations and alkenone temperatures in suspended particles collected from the subsurface waters in early fall indicated that these compounds were produced mostly in a surface mixed layer above the depth of the chlorophyll maximum even in warm seasons. These results suggested that alkenone temperatures strongly reflected SST rather than the temperatures of thermocline waters in these study areas even in such a warm season. Pronounced maxima in A&A fluxes found in sediment trap samples at 1674 m in late spring to summer showed that A&A productions were highest during the periods of spring bloom, according to a time delay between alkenone temperatures and observed SST. Seasonal patterns of alkenone records in trap samples at 4180 and 5687 m could also preserve SST signals well, suggesting that A&A in deep sea waters were mainly derived from primary products in the surface layer. A&A fluxes tended to decrease with water depth, and the ratios of A&A to particulate organic carbon (POC) rapidly decreased in underlying bottom sediment. This clearly indicates that A&A were decomposed and diluted by other refractory organic materials in either the water column or the sediment–water interface. However, A&A compositions were consistently uniform between the trap samples and the underlying bottom sediments, so that A&A could not qualitatively alter during early diagenetic processes.     

Characteristics of crustal structures in the Yamato Basin,sea of Japan,deduced from seismic explorations

Crustal structures around the Yamato Basin in the southeastern Sea of Japan, inferred from recent ocean bottom seismography (OBS) and active-source seismological studies, are reviewed to elucidate various stages of crustal modification involved from rifting in the crust of the surrounding continental arc to the production of oceanic crust in the Yamato Basin of the back-arc basin. The northern, central, and southern areas of the Yamato Basin have crustal thicknesses of approximately 12–16 km, and lowermost crusts with P-wave velocities greater than 7.2 km/s. Very few units have P-wave velocities in the range 5.4–6.0 km/s, which corresponds to the continental upper crust. These findings, combined with previous geochemical analysis of basalt samples, are interpreted to indicate that a thick oceanic crust has been formed in these areas of the basin, and that this oceanic crust has been underplated by mantle-derived magma. In the central Yamato Basin, the original continental crust has been fully breached and oceanic crust has been formed. Conversely, the presence of a unit corresponding to the continental upper crust and the absence of a high-velocity part in the lower crust implies that the southwestern edge of the Yamato Basin has a rifted crust without significant intrusion. The Oki Trough has a crust that is 17–19 km thick with a high-velocity lower crust and a unit corresponding to the continental upper crust. The formation of the Oki Trough resulted from rifting with magmatic intrusion and/or underplating. We interpret these variations in the crustal characteristics of the Yamato Basin area as reflecting various instances of crustal modification by thinning and magmatic intrusion due to back-arc extension, resulting in the production of a thick oceanic crust in the basin.     

Wind-Tunnel and Numerical Simulations of the Coastal Thermal Internal Boundary Layer

Wind-tunnel experiments in a thermally stratified wind tunnel and direct numerical simulations were performed to simulate the thermal internal boundary layer (TIBL) that developed over a coastal area in a sea-breeze flow. The results of the simulations were analyzed to investigate turbulence structure in the TIBL. To study the effects of the atmospheric stability over the sea on the TIBL, two vertical profiles of temperature were created in the upstream portion of the wind-tunnel experiment and the direct numerical simulation. Turbulence statistics of the TIBL changed significantly according to the temperature profile over the sea, indicating that the stability of the flow over the sea has a significant effect on the structure and turbulence characteristics of the TIBL. Furthermore, the TIBL heights were estimated from the vertical profiles of the local Richardson number. The estimated TIBL heights agreed with those predicted by a pre-existing relation, suggesting that both the wind-tunnel experiment and the direct numerical simulation accurately reproduced the growth of the TIBL.     

Interactions of uranium with bacteria and kaolinite clay

We assessed the accumulation of uranium (VI) by a bacterium, Bacillus subtilis, suspended in a slurry of kaolinite clay, to elucidate the role of microbes on the mobility of U(VI). Various mixtures of bacteria and the koalinite were exposed to solutions of 8 × 10^− 6 M- and 4 × 10^− 4 M-U(VI) in 0.01 M NaCl at pH 4.7. After 48 h, the mixtures were separated from the solutions by centrifugation, and treated with a 1 M CH₃COOK for 24 h to determine the associations of U within the mixture. The mixture exposed to 4 × 10^− 4 M U was analyzed by transmission electron microscope (TEM) equipped with EDS. The accumulation of U by the mixture increased with an increase in the amount of B. subtilis cells present at both U concentrations. Treatment of kaolinite with CH₃COOK, removed approximately 80% of the associated uranium. However, in the presence of B. subtilis the amount of U removed was much less. TEM–EDS analysis confirmed that most of the U removed from solution was associated with B. subtilis. XANES analysis of the oxidation state of uranium associated with B. subtilis, kaolinite, and with the mixture containing both revealed that it was present as U(VI). These results suggest that the bacteria have a higher affinity for U than the kaolinite clay mineral under the experimental conditions tested, and that they can immobilize significant amount of uranium.     

Mid- and far-infrared extinction coefficients of hydrous silicate minerals

Extinction coefficients were measured for three kind of hydrous silicate minerals, montmorillonite, chlorite and serpentine, from 7 to 140 m. The infrared extinction coefficients of these minerals show (1) a few broad bands in the mid-infrared region and (2) a less steep wavelength-dependence in the far-infrared region, in contrast to those of high-temperature magnesium silicates. In the far-infrared region, montmorillonite shows a ^–0.8±0.1 dependence (, the wavelength) without any band structure, chlorite has a double maxima structure around 80 m, and serpentine shows a rather steep dependence with a small peak at 77 m.The changes of mid-infrared spectra by heating were measured. Change in chlorite spectrum is the most significant. Many fine features appear by heating and then they disappear. Above 900°C one broad feature remains around 10 m. Fine features of the montmorillonite spectrum disappear by heating. For serpentine, many new peaks appear and the spectrum resembles the spectrum of olivin. In near-infrared a band around 2.72 m disappears by heating.Extinction coefficients at very low temperatures were measured in the far-infrared region. For montmorillonite and serpentine, the spectrum is the same as that at room temperature. The double peaks of chlorite around 80 m become higher.     

Phase equilibria and the pressure-temperature path of the highest-grade Ryoke metamorphic rocks in the Yanai district, SW Japan

The garnet-cordierite zone, the highest-grade zone of the Ryoke metamorphic rocks in the Yanai district, SW Japan, is defined by the coexistence of garnet and cordierite in pelitic rocks. Three assemblages in this zone are studied in detail, i.e. spinel + cordierite + biotite, garnet + cordierite + biotite and garnet + biotite, all of which contain quartz, K-feldspar and plagioclase. The Mg/(Fe + Mg) in the coexisting minerals decreases in the following order: cordierite, biotite, garnet and spinel. Two facts described below are inconsistent with the paragenetic relation in the K₂OFeOMgOAl₂O₃SiO₂H₂O (KFMASH) system in terms of an isophysical variation. First, garnet and biotite in the last assemblage have Mg/(Fe + Mg) higher than those in the second. Second, the first two assemblages are described by the reaction,