Direct evidence for nitrogen isotope discrimination during sedimentation and early diagenesis in Lake Kasumigaura, Japan

Sediment core samples from the center of Lake Kasumigaura, Japan, were collected from 1979 to 2007 at intervals of 1 month to 5 yr. We evaluated the degree of modification in N isotope composition during sedimentation and diagenesis. We estimated the degree of isotope discrimination during diagenesis by comparing historical changes in N isotope composition of the surface sediment (top 2 cm) against the vertical profile of the isotope composition of sediment core samples (15 cm depth). The degree of ¹⁵N enrichment during sedimentation appeared to be significant under the preferential N decomposition that occurred in the periods with low C/N ratio values of suspended particulate organic matter. We documented ¹⁵N depletion in sediment deeper than approximately 3 cm during diagenesis. The contrasting directions of N isotope discrimination during sedimentation and diagenesis suggest changing mechanisms of isotopic shift across an oxidation-reduction boundary.     

Effects of transport of pore water and material heterogeneity on strain localization of fluid‐saturated gradient‐dependent viscoplastic geomaterial

The purpose of the present paper is to clarify the effects of permeability and initial heterogeneity on the strain localization of fluid‐saturated cohesive soil modelled by a strain gradient‐dependent poro‐viscoplastic constitutive model. The effects of permeability and gradient parameters on the growth rate of the fluctuation were obtained by a linear instability analysis. Deformation behaviour of clay specimens modelled as a viscoplastic model with a second order strain gradient during shear was numerically analysed by a soil–water coupled FEM under both globally undrained and partially drained conditions. It was found that the deformation pattern and the stress–strain curve greatly depend on the permeability, the drainage conditions and the initial non‐homogeneous properties. Copyright © 2005 John Wiley & Sons, Ltd.     

Phase relations in the carbon-saturated C–Mg–Fe–Si–O system and C and Si solubility in liquid Fe at high pressure and temperature: implications for planetary interiors

The phase and melting relations of the C-saturated C–Mg–Fe–Si–O system were investigated at high pressure and temperature to understand the role of carbon in the structure of the Earth, terrestrial planets, and carbon-enriched extraterrestrial planets. The phase relations were studied using two types of experiments at 4 GPa: analyses of recovered samples and in situ X-ray diffractions. Our experiments revealed that the composition of metallic iron melts changes from a C-rich composition with up to about 5 wt.% C under oxidizing conditions (ΔIW = ?1.7 to ?1.2, where ΔIW is the deviation of the oxygen fugacity (fO₂) from an iron-wüstite (IW) buffer) to a C-depleted composition with 21 wt.% Si under reducing conditions (ΔIW < ?3.3) at 4 GPa and 1,873 K. SiC grains also coexisted with the Fe–Si melt under the most reducing conditions. The solubility of C in liquid Fe increased with increasing fO₂, whereas the solubility of Si decreased with increasing fO₂. The carbon-bearing phases were graphite, Fe₃C, SiC, and Fe alloy melt (Fe–C or Fe–Si–C melts) under the redox conditions applied at 4 GPa, but carbonate was not observed under our experimental conditions. The phase relations observed in this study can be applicable to the Earth and other planets. In hypothetical reducing carbon planets (ΔIW < ?6.2), graphite/diamond and/or SiC exist in the mantle, whereas the core would be an Fe–Si alloy containing very small amount of C even in the carbon-enriched planets. The mutually exclusive nature of C and Si may be important also for considering the light elements of the Earth’s core.     

Dissolved organic carbon in a eutrophic lake; dynamics,biodegradability and origin

The seasonal and spatial changes in dissolved organic carbon (DOC) in Lake Kasumigaura, a shallow, eutrophic lake, were analyzed and the lability of DOC was tested by long-term incubations. There was a nearly 1 mgCl^–1 downstream increase in refractory DOC in the lake; at the center it fluctuated little seasonally. The characteristic UV-absorbance: DOC ratios were determined for samples from the influent rivers (pedogenic: used interchangeably with allochthonous) and outdoor experimental ponds (autochthonous) during incubations. These ratios were then used to calculate the proportion of total measured lake water DOC in each of four components: pedogenic-refractory (PR), pedogenic-labile (PL), autochthonous-refractory (AR) and autochthonous-labile (AL). PR was uniform (around 1.5 mgCl^–1) or diminished very slightly over time. AR increased from nearly zero at the station closest to an influent river to 1 mgCl^–1 at the lake center. PL declined downstream from 0.3 mgCl^–1 to zero. AL was virtually constant at 0.8 mgCl^–1 except at the station closest to the influent river. The constancy of the UV-absorbance: DOC ratio during the biodegradation process was confirmed for Lake Kasumigaura; hence a two-component model (pedogenic-autochthonous) could be applied here without consideration of DOC lability. However, this assumption is not always met for other water bodies, and therefore it should be checked before applying a two-component model elsewhere.     

A direct numerical approach to the Chandrasekhar'sH-functions for arbitrary characteristic functions

The purpose of this paper is to present a numerical technique to directly compute the Chandrasekhar'sH ()-function for anisotropic scattering in terms of the roots of the characteristic equations as well as the quadrature points of a certain degreen employed to approximate the definite integral involved in the basic equation. The principal feature of the algorithm proposed here is a compact computer code to enumerate _n C _m combinations ofn distinct integers {1,...,n} takenm at a time. With these quantities available, the coefficients of the polynomial equation of the characteristics equation can be readily computed for any given characteristic function, so that a standard technique such as the Laguerre method can be applied to find all the roots.It is shown that the results obtained for some representativeH()-functions using the present technique with relatively low-order formula (e.g.,n=7) are sufficiently accurate for all practical purposes.     

Some regular patterns in the distribution of sediment contamination in the coastal waters along Japan

Observations of sediment contamination along the coast of Japan were analyzed. When the pollutant concentration is divided by the fine particle fraction in the sediment, a regular pattern is observed in the quantitative relationship among the degree and the area of contamination and the discharge rate of pollutant released continuously into the water along the coast. This regularity was observed with respect to COD,n-hexane soluble substances and heavy metals, and could be expressed by a formula.Polluted particles were supposed to disperse through suspension in the bottom water layer, and thus their distribution in the surface sediment is expected to become similar to effluent dispersion in the surface water.     

Structure of the strong tidal jet in the naruto strait

In order to clarify the structure of the strong tidal current at the Naruto Strait in the Seto Inland Sea of Japan, the sea-level values were observed in the strait and the current measurements were made with an Acoustic Doppler Current Profiler (ADCP).The tidal volume transports for M₂ and S₂ tides were about 74×10³ and 26×10³ m³ sec^–1, respectively. The horizontal profile of the velocity at the phase of the strong tidal current compares favorably with a theoretical profile of the two-dimensional steady turbulent jet except for the side parts of the profile. Moreover, the entrainment rate of the surrounding water into the strong tidal jet was estimated from the difference of mass flux between two cross-sections at the strait, the entrainment rate and entrainment constant for both the northward and southward flows being about 1.3–2.5×10^–4m^–1 and about 0.03–0.05, respectively.     

High-pressure X-ray diffraction and Raman spectroscopy of CaFe<Subscript>2</Subscript>O<Subscript>4</Subscript>-type β-CaCr<Subscript>2</Subscript>O<Subscript>4</Subscript>

In situ high-pressure synchrotron X-ray diffraction and Raman spectroscopic studies of orthorhombic CaFe₂O₄-type β-CaCr₂O₄ chromite were carried out up to 16.2 and 32.0 GPa at room temperature using multi-anvil apparatus and diamond anvil cell, respectively. No phase transition was observed in this study. Fitting a third-order Birch–Murnaghan equation of state to the P–V data yields a zero-pressure volume of V ₀ = 286.8(1) ų, an isothermal bulk modulus of K ₀ = 183(5) GPa and the first pressure derivative of isothermal bulk modulus K ₀′ = 4.1(8). Analyses of axial compressibilities show anisotropic elasticity for β-CaCr₂O₄ since the a-axis is more compressible than the b- and c-axis. Based on the obtained and previous results, the compressibility of several CaFe₂O₄-type phases was compared. The high-pressure Raman spectra of β-CaCr₂O₄ were analyzed to determine the pressure dependences and mode Grüneisen parameters of Raman-active bands. The thermal Grüneisen parameter of β-CaCr₂O₄ is determined to be 0.93(2), which is smaller than those of CaFe₂O₄-type CaAl₂O₄ and MgAl₂O₄.     

Lattice preferred orientation in CaIrO<Subscript>3</Subscript> perovskite and post-perovskite formed by plastic deformation under pressure

Lattice preferred orientations (LPO) developed in perovskite and post-perovskite structured CaIrO₃ were studied using the radial X-ray diffraction technique combined with a diamond anvil cell. Starting materials of each phase were deformed from 0.1 MPa to 6 GPa at room temperature. Only weak LPO was formed in the perovskite phase, whereas strong LPO was formed in the post-perovskite phase with an alignment of the (010) plane perpendicular to the compression axis. The present result suggests that the (010) is a dominant slip plane in the post-perovskite phase and it is in good agreement with the crystallographic prediction, dislocation observations via transmission electron microscopy, and a recent result of simple shear deformation experiment at 1 GPa–1,173 K. However, the present result contrasts markedly from the results on MgGeO₃ and (Mg,Fe)SiO₃, which suggested that the (100) or (110) is a dominant slip plane with respect to the post-perovskite structure. Therefore it is difficult to discuss the behavior of the post-perovskite phase in the Earth’s deep interior based on existing data of MgGeO₃, (Mg,Fe)SiO₃ and CaIrO₃. The possible sources of the differences between MgGeO₃, (Mg,Fe)SiO₃ and CaIrO₃ are discussed.     

Effect of incorporation of iron and aluminum on the thermoelastic properties of magnesium silicate perovskite

In situ X-ray diffraction measurements of Fe- and Al-bearing MgSiO₃-rich perovskite (FeAl-Pv), which was synthesized from a natural orthopyroxene, were performed at pressures of 19–32 GPa and temperatures of 300–1,500 K using a combination of a Kawai-type apparatus with eight sintered-diamond anvils and synchrotron radiation. Two runs were performed using a high-pressure cell with two sample chambers, and both MgSiO₃ perovskite (Mg-Pv) and FeAl-Pv were synthesized simultaneously in the same cell. Thus we were able to measure specific volumes (V/V ₀) of Mg-Pv and FeAl-Pv at the same P−T conditions. At all the measurement conditions, values of the specific volume of FeAl-Pv are consistent with those of Mg-Pv within 2 Standard Deviation, strongly suggesting that effect of incorporation of iron and aluminum on the thermoelastic properties of magnesium silicate perovskite is undetectable in this composition, pressure, and temperature range. Two additional runs were performed using a high-pressure cell that has one sample chamber and unit-cell volumes of FeAl-Pv were measured at pressures and temperatures up to 32 GPa and 1,500 K, respectively. All the unit-cell volume data of FeAl-Pv perovskite were fitted to the high temperature Birch–Murnaghan equation of state and a complete set of thermoelastic parameters of this perovskite was determined with an assumption of K′ _300,0 = 4. The determined parameters are K _300,0 = 243(3) GPa, (∂K _T,0/∂T) _P = −0.030(8) GPa/K, a ₀ = 2.78(18) × 10⁻⁵ K⁻¹, and b ₀ = 0.88(28) × 10⁻⁸ K⁻², where a ₀ and b ₀ are the coefficients of the following expression describing the zero-pressure thermal expansion: α _T,0 = a ₀ + b ₀ T. The equation-of-state parameters of FeAl-Pv are in good agreement with those of MgSiO₃ perovskite at the conditions corresponding to the uppermost part of the lower mantle.