Multi‐species diffusion analysis in porous media under various dry density and temperature conditions: molecular dynamics simulation,homogenization analysis,and finite element method

In porous media, chemical species that dissolve in pore water can be transported via diffusion mechanisms or advective fluxes, close to or far away from where precipitation occurs. In the case of a high‐level radioactive waste disposal system, compacted bentonite is used in a buffer material in an engineering barrier system to minimize the amount of specific nuclides that breach into the surrounding host rock. To minimize breaching, it is very important to understand the transport mechanism of multiple chemical species in porous media. In the following research, we introduced FEM analysis methods using the results of the molecular dynamics simulation and homogenization analysis (MD/HA) method. First, the diffusion coefficients of ions (Cl^?, I^?, and Na⁺) in different water layers of Na‐beidellite were calculated using the MD/HA procedure under various dry density (1.2, 1.6, and 2.0 Mg/m³) and temperature (293, 323, and 363 K) conditions. Next, using FEM analysis that used the MD/HA results as input parameters, the diffusion behaviors of ions in porous media were calculated. The results indicate that the diffusion coefficients of the interlayer water in Na‐beidellite are different from the diffusion coefficients under dry density conditions. Further, the concentration profiles (C_t/C₀) of iodine and chloride are proportional to temperature but inversely proportional to dry density. Copyright © 2014 John Wiley & Sons, Ltd.     

Accretion and tectonic erosion processes revealed by the mode of occurrence and geochemistry of greenstones in the Cretaceous accretionary complexes of the Idonnappu Zone, southern central Hokkaido, Japan

The Cretaceous accretionary complexes of the Idonnappu Zone in the Urakawa area are divided into five lithological units, four of which contain greenstone bodies. The Lower Cretaceous Naizawa Complex consists of two lithologic units. The Basaltic Unit (B‐Unit) is a large‐scale tectonic slab of greenstone, consisting of depleted tholeiite similar to that of the Lower Sorachi Ophiolite (basal forearc basin ophiolite) in the Sorachi‐Yezo Belt. The Mixed Unit of Naizawa Complex (MN‐Unit) contains oceanic island‐type alkaline greenstones which occur as slab‐like bodies and faulted blocks with tectonically dismembered trench‐fill sediments. Repeated alternations of the two units in the Naizawa Complex may have been formed by the collision of seamounts with forearc ophiolitic body (Lower Sorachi Ophiolite) in the trench. The Upper Cretaceous Horobetsugawa Complex structurally underlies the Naizawa Complex in its original configuration, and it also contains greenstone bodies. Greenstones in the MH‐Unit occur as blocks and sedimentary clasts in a clastic matrix, and exhibit depleted tholeiite and oceanic‐island alkaline basalt/tholeiite chemistry. This unit is interpreted as submarine slide and debris flow deposits. Greenstones in the PT‐Unit occur at the base of several chert‐clastic successions. Most of the greenstones are severely sheared and show normal‐type mid‐ocean ridge basalt composition. The PT‐Unit greenstones are considered to have been derived from abyssal basement peeled off during accretion. The different accretion mechanism of the greenstones in the Naizawa and Horobetsugawa complexes reflects temporal changes in subduction zone conditions. Seamount accretion and tectonic erosion were dominant in the Early Cretaceous, due to highly oblique subduction of the old oceanic crust and minimal sediment supply. Whereas, thick sediments with minor mid‐ocean ridge basalt and olistostrome accreted in the Late Cretaceous, due to near‐orthogonal subduction of young oceanic crust with voluminous sediment supply.     

Modification of SAR spectra associated with surface wind fields in the sea off the Kii Peninsula: A case study

Using surface wave parameters and a high-resolution surface wind field derived from Synthetic Aperture Radar (SAR) image mode data, we have investigated the spatial modification of SAR spectra. We found a surface wind front, formed by sheltering effect of the Kii Mountains, separating high and low wind-speed regions in a sea area of an European Remote-Sensing Satellite (ERS) SAR image off the Kii Peninsula. A swell system propagating westward dominates in the whole sea area covered by the SAR image. The wavelength retrieved from the SAR spectra in the sheltered (non-sheltered) region is longer (shorter). Since the distributions of surface wave parameters and surface wind speed are so well correlated, it can be considered that the SAR spectra are modified differently by the sheltered/non-sheltered surface winds. In order to examine the phenomena observed on the SAR image we have estimated the wind-wave SAR spectrum using the SAR surface winds, a wind-wave spectrum model and a SAR wave imaging model. We assume that the SAR spectrum related to the swell is homogeneous in the area imaged by SAR, and that the SAR spectrum of the wind-wave components causes the observed SAR spectra modification. Differences between the observed SAR spectra and the estimated SAR spectra in the sheltered and non-sheltered regions agree well with each other. In the present case, it can be concluded that the observed SAR spectra can be regarded as a linear combination of the wind-wave SAR spectra and the swell SAR spectra.     

Tightly bound aliphatic acids in Lake Biwa sediments: Their origin and stability

Tightly bound geolipids were separated from a 200 m sediment core of Lake Biwa by a second saponification of sediments from which unbound and bound lipids had been extracted. Tightly bound fatty acids, β-hydroxy acids, ω-hydroxy acids and α,ω-dicarboxylic acids were released; their concentrations ranged from 4.7–31.5, 5.6–60.5, 3.4–9.5 and 0.2–5.4 μg/g dry sediment, respectively. These geolipids were considered to be incorporated in humic substances.Tightly bound fatty acids showed a unimodal distriution with a peak at C₁₆, suggesting that they originate from algae and bacteria and that they are more stable than unbound and bound fatty acids in the sediments. Most of the total β-hydroxy acids, which probably originate from bacteria, were found in the tightly bound fraction. This suggests that a large portion of tightly bound geolipids are formed in the water column and in surface sediments as a result of microbial alteration dead algae. Each class of tightly bound lipids showed higher concentrations between depths of 3 and 15 m in the sediments, where primary production was thought to be enhanced in the past.     

Sequential forecasting of the surface and subsurface conditions in the Japan Sea

This study estimates a realistic change of the Japan Sea by assimilating satellite measurements into an eddy-resolving circulation model. Suboptimal but feasible assimilation schemes of approximate filtering and nudging play essential roles in the system. The sequential update of error covariance significantly outperforms the asymptotic covariance in the sequential assimilation due to the irregular sampling patterns from multiple altimeter satellites. The best estimates show an average rms difference of only 1.2°C from the radiometer data, and also explain about half of the sea level variance measured by the altimeter observation. The subsurface conditions associated with the mesoscale variabilities are also improved, especially in the Tsushima Warm Current region. It is demonstrated that the forecast limit strongly depends on variable, depth, and location.     

The spatial and seasonal distributions of air-transport origins to the Antarctic based on 5-day backward trajectory analysis

Transport of moisture-bearing air to the Antarctic is one of the important factors that control the mass balance of the ice sheet. Here, we investigate the distribution of air-parcel transport using a backward trajectory analysis over the entire Antarctic ice sheet, based on whether the air parcel was located inside or outside of Antarctica at 5 days before arrival. At this time, we considered the air from outside Antarctica to be moisture rich. Oceanic air was found to dominate in West Antarctica throughout the year, whereas air from inland was more prominently distributed around East Antarctica, especially in summer. In East Antarctica, there was a significant seasonal variation: air from inland dominated in summer, while air of oceanic origin dominated in winter. The distribution of air parcels that came from oceanic/inland sources was similar to the accumulation map (based on satellite data), which indicates that oceanic air parcels could be a substitute for moisture transport to the Antarctic. To determine the future impacts of climate change (e.g., sea level rise), more precise predictions of the variations in the surface mass balance will be required. Our results contribute towards the improved understanding of the spatial distributions of accumulation and aerosols found in Antarctic snow and ice cores.     

Distributions of low molecular weight dicarboxylic acids in the North Pacific aerosol samples

Marine aerosol samples collected from the North Pacific atmosphere were studied for molecular distributions of dicarboxylic acids by using a capillary gas chromatography and mass spectrometery. A homologous series of dicarboxylic acids (C₂–C₁₀) was detected in the marine aerosol samples as dibutyl esters. All the samples showed that the smallest diacid (oxalic acid: C₂) was the most abundant and comprised 41–67% of the total diacids. The second most abundant species was malonic acid (C₃) or succinic acid (C₄). The diacids with more carbon numbers were generally less abundant. Total diacid concentration range was 17–1040 ng m^–3, which accounted for up to 1.6% of total aerosol mass. This indicates that low molecular weight dicarboxylic acids are important class of organic compounds in the marine atmosphere. The concentrations were generally higher in the western North Pacific and lower in the central North Pacific. The major portion of diacids is probably derived from the Asian Continent and East Asian countries by long-range atmospheric transport and partly fromin situ photochemical production in the marine atmosphere.     

Numerical experiment for strontium-90 and cesium-137 in the Japan Sea

A numerical experiment is carried out to reproduce distribution of concentration of ⁹⁰Sr and ¹³⁷Cs, estimate their total amount and verify their source in the Japan Sea. Model results are in good agreement with observational findings in the Japan Sea expeditions between 1997 and 2002 by the Japan Atomic Energy Agency. Vertical profiles of the concentration of ⁹⁰Sr and ¹³⁷Cs show exponential decreases with depth from the sea surface to the sea bottom. From the model and observational results, it is suggested that the concentration of ⁹⁰Sr and ¹³⁷Cs in the surface layer is approximately in the range of 1.0–1.5 Bq/m³ and 2.0–2.5 Bq/m3, respectively. On the other hand, it is found that the concentration in the intermediate and deep layer is higher than that observed in the northwestern Pacific Ocean, suggesting active winter convection in the Japan Sea. The total amount of ⁹⁰Sr and ¹³⁷Cs in the seawater is evaluated to be 1.34 × 10¹⁵ Bq and 2.02 × 10¹⁵ Bq, respectively, in the numerical experiment, which demonstrates an estimation by observational data obtained in the Japan Sea expeditions. The total amount of ⁹⁰Sr and ¹³⁷Cs changed during the second half of 20th century corresponding to deposition at the sea surface with the maximums of 4.86 × 10¹⁵ Bq for ⁹⁰Sr and 7.33 × 10¹⁵ Bq for ¹³⁷Cs, respectively, in the mid-1960s. The numerical experiment suggests that the main source of ⁹⁰Sr and ¹³⁷Cs has been global fallout, although there have been some potential sources in the Japan Sea.     

Rayleigh scattering by aqueous colloidal silica as a cause for the blue color of hydrothermal water

Thermal waters in hydrothermal ponds, bathing pools and the brines of geothermal electric power plants commonly have a characteristic blue color. Although many researchers have assumed that the blue color is due to a colloidal suspension and/or absorption by dissolved ferrous iron or by water itself, there has been no specific effort to identify the physical nature of this phenomenon. We have tested, in synthetic and natural solutions, whether aqueous colloidal silica is responsible for the blue color. Aqueous colloidal silica is formed by silica polymerization in thermal waters of the neutral-chloride type which contain initially monomeric silica in concentrations up to three times above the solubilities of amorphous silica. The hue of the blue thermal waters in the pools tested agrees with that of a synthesized colloidal silica solution. Grain-size analyses of aqueous colloidal silica in the blue-colored thermal waters demonstrate that the color is caused by Rayleigh scattering from aqueous colloidal silica particles with diameters (0.1–0.45 μm) smaller than the wavelengths of visible radiation.     

Seasonal changes in stable carbon isotopic composition of n-alkanes in the marine aerosols from the western North Pacific: Implications for the source and atmospheric transport

To constrain seasonal changes in the long-range atmospheric transport of land-derived lipid biomarker compounds, we investigated the compound-specific stable isotopic composition of marine aerosol n-alkanes collected from 1990 to 1993 at a remote island, Chichi-Jima (27°04′N, 142°13′E), in the western North Pacific. Compound-specific isotope analysis revealed, in particular, strong seasonal changes in the δ¹³C values of the C₂₉ and C₃₁n-alkanes (biomarkers for higher plants). Lighter δ¹³C values were observed in winter (typically −32 to −34‰), with a transition to heavier values in summer (typically −28 to −31‰). Using a mixing equation and typical end members for C₃ and C₄ plants, we found that this is due to relative increases in the contributions from C₄ plants in the summer season. Using backward air-mass trajectory analyses, it was shown that the Asian continent was the major source region for C₃ plant material during winter/spring, whereas Indonesia/Australia and possibly the Americas were the major source regions for C₄ material during the summer/autumn. Also observed was an enhanced atmospheric transport of n-alkanes from C₄ plants in 1991 summer/autumn during a strong El Nino event, which was associated with forest and bushfires in Indonesia and Australia. In addition to providing information on contemporary processes, this study also provides a base for future paleoclimatological work in ocean sediments.