Hydrostatic compression of ilmenite phase of ZnSiO3 and MgGeO3

Accurate measurements of cell parameters were performed on the ilmenite phases of ZnSiO₃ and MgGeO₃ using an X-ray diffraction method under hydrostatic conditions. The linear changes in cell parameter are represented by 1?a/a ₀=(1.06±0.04)×10^?4 P(kbar) and 1?c/c ₀=(2.11±0.04)×10^?4 P for ZnSiO₃, and 1?a/a ₀=(1.37±0.03)×10^?4 P and 1?c/c ₀=(2.05±0.04)×10^?4 P for MgGeO₃. A least-squares calculation using the first-order Birch-Murnaghan equation gives K _T =2.16±0.02 Mbar and K _T =1.87±0.02 Mbar for ZnSiO₃ and MgGeO₃, respectively. Elastic systematics assuming K _T V _m =constant give a predicted value K _T =2.14 Mbar for the ilmenite phase of MgSiO₃.     

Partition of magnesium and iron between Olivine and spinel,and between pyroxene and spinel

Partition of Fe²⁺ and Mg between coexisting (Mg, Fe)₂SiO₄ spinel and (Mg, Fe)SiO₃ pyroxene was investigated at pressures 80 and 90 kbar and at temperatures 840 and 1050° C, using tetrahedral-anvil type of high pressure apparatus. Olivine-spinel solid solution equilibria in the system Mg₂SiO₄-Fe₂SiO₄ were discussed in the light of the partition reaction. Partition of Fe²⁺ and Mg in both olivine-spinel and pyroxene-spinel systems can not be regarded as that between ideal solid solutions. By applying the simple solution model for the partition of Fe²⁺ and Mg, sign of the heat of mixing was estimated to be positive for all olivine, spinel and pyroxene. Relative concentration of Fe²⁺ in spinel in the pyroxene-spinel system is likely to cause some change in the chemical composition of modified spinel () or spinel () in the transition zone of the mantle. A considerable change is also expected in the transition pressure of to ( + ) and ( + ) to .Presented at the symposium Recent Advances in the Studies of Rocks and Minerals at High Pressures and Temperatures held in Montreal, 1972. Jointly sponsored by the International Mineralogical Association and the Commission on Experimental Petrology.     

Characterization of the amorphous state in metamict silicates and niobates by EXAFS and XANES analyses

X-ray absorption spectroscopy using synchrotron radiation has been applied to the investigation of the coordination geometries around Y, Zr and Nb atoms in metamict zircon, gadolinite, fergusonite, euxenite and samarskite. EXAFS and XANES spectra of their crystalline counterparts and synthetic compounds including ZrO₂, Y₂O₃, YNbTiO₆, YNbO₄, LiNbO₃, and NiNb₂O₆ were also measured for comparison. Metamict zircon shows a significant decrease in its Zr-O bond distances accompanying an increase in distortion of the Zr-O coordination polyhedra as compared with crystalline zircon. On the contrary, the average Nb-O bond distances and the symmetry of the coordination polyhedra around the Nb atoms in metamict euxenite and samarskite resemble those in the crystalline euxenite. Compared with crystalline fergusonite, a decrease in the distortion of the Nb-O octahedra is observed in metamict fergusonite. The structures of the second nearest neighbors (the metal-metal interactions) are largely disrupted in the metamict specimens except for metamict zircon and samarskite with high trivalent iron concentration. Nb in metamict samarskite is in octahedral coordination by oxygen and is similar to that in euxenite.     

Electron probe microanalysis study on processes of low-temperature oxidation of titanomagnetite

Partially oxidized titanomagnetite grains in various kinds of volcanic rocks were investigated by electron probe microanalyzer (EPMA) in order to clarify the process of oxidation at low temperature. The following results were obtained by the present investigation: (1) Primary composition of titanomagnetite is homogeneous in individual grains, although variation in composition among different grains is observed on each thin section. (2) Migration of Fe cations during low-temperature oxidation is clearly seen in all oxidized grains. Some other constituent cations are also bleached and consequently the relative content of the remaining cations becomes large. (3) The detailed internal structures of titanomagnetite grains are observed as backscattered electron images (BEI) with an electronprobe microanalyzer, and it seems likely that the structures depend upon the degree of low-temperature oxidation. (4) The chemical and physical properties of oxidized titanomagnetites imply that low-temperature oxidation is not a simple process but a complex one. Such an oxidation process is correlatable to both the mobility of cation and the oxidation condition such as a circulation of some active hydrothermal materials at low temperature.     

Elasticity of the olivine and spinel polymorphs of Ni2SiO4

The single-crystal elastic moduli, c _ij x, of the olivine (α) and spinel (γ) polymorphs of nickel orthosilicate have been measured at atmospheric pressure and 20° C by Brillouin spectroscopy. The results are (Mbar), Ni₂SiO₄ olivine: c ₁₁=3.40(2), c ₂₂=2.38(2), c ₃₃=2.53(2), c ₄₄=0.71(1), c ₅₅=0.87(1), c ₆₆=0.78(1), c ₁₂=1.09(2), c ₁₃=1.10(4), c ₂₃=1.13(3), Ni₂SiO₄ spinel: c ₁₁=3.66(3), c ₄₄=1.06(1), c ₁₂=1.55(3). In comparing these results with extant elasticity data for olivine- and spinel-type compounds we find distinctive elastic characteristics related to crystal structure, and systematic trends due only to compositional variation. For silicate olivines, the longitudinal moduli decrease in the order c ₁₁>c ₃₃>c ₂₂, regardless of composition. The moduli c ₅₅ and c ₆₆ are approximately equal, and greater than c ₄₄. The former relationship is related to differences in polyhedral linkages along the crystallographic axes, whereas the latter may result from rotational freedom of SiO₄ tetrahedra in response to different directions of shear. Composition affects elasticity most directly through the relative magnitudes of \(\bar c_{12} > \; = (c_{12} + c_{13} + c_{23} )/3\) and \(\bar c_{44} = (c_{44} + c_{55} + c_{66} )/3\) . When transition-metal cations are six-coordinated by oxygen \(\bar c_{12} > \bar c_{44}\) , and when alkaline-earth cations are six-coordinated \(\bar c_{44} > \bar c_{12}\) . The longitudinal moduli along and normal to the close-packed directions of spinels are similar, reflecting the framework-like arrangement of octahedra. These longitudinal moduli exhibit little compositional dependence upon tetrahedral cations but vary dramatically with octahedral substitution. Our data indicate that tetrahedral cations affect elastic properties more as the oxygen positional parameter, u, decreases. The u parameter is also directly related to elastic anisotropy. While γ-Ni₂SiO₄ (u=0.244) is elastically isotropic, anisotropy increases rapidly as u approaches a limiting value near 0.27, and may be related to mechanical stability of the spinel structure. The longitudinal wave velocities along close-packed directions in α and γ Ni₂SiO₄ are equal. Thus, for an α-γ polymorphic pair, the assumptions of elastic isotropy of the γ phase and equal velocities in close-packed directions of α and γ allows the c _ij's and shear modulus of a spinel-structure silicate to be estimated from c ₁₁ of the corresponding α phase and the bulk modulus of the γ phase.     

Impacts of different diffusion scenarios for mitigation technology options and of model representations regarding renewables intermittency on evaluations of CO2 emissions reductions

This paper evaluated the impacts of climate change mitigation technology options on CO₂ emission reductions and the effects of model representations regarding renewable intermittency on the assessment of reduction by using a world energy systems model. First, different diffusion scenarios for carbon dioxide capture and storage (CCS), nuclear power, and wind power and solar PV are selected from EMF27 scenarios to analyze their impacts on CO₂ emission reductions. These technologies are important for reducing CO₂ intensity of electricity, and the impacts of their diffusion levels on mitigation costs are significant, according to the analyses. Availability of CCS in particular, among the three kinds of technologies, has a large impact on the marginal CO₂ abatement cost. In order to analyze effects of model representations regarding renewables intermittency, four different representations are assumed within the model. A simplistic model representation that does not take into consideration the intermittency of wind power and solar PV evaluates larger contributions of the energy sources than those evaluated by a model representation that takes intermittency into consideration. Appropriate consideration of renewables intermittency within global energy systems models will be important for realistic evaluations of climate change mitigation scenarios.     

First-Aid Transportation by Hovercraft in a Disaster

Transportation is one of the most important and urgent tasks in a disaster, e.g., earthquake or flood. Trains, trucks and cars are very restricted by destruction of rail and road, bridges and buildings fall down, flood waters and thick mud, landslides, cracks, level differences, severe traffic jam etc. Sunken objects in the water and damages of quays prevent ships from reaching harbors. The situation remains days, weeks and even months.Hovercraft can run on almost every surface: ground, water surface, mud, sands, grits, weeds etc. The performance is very favorable in the first-aid transportation in a disaster.A middle size hovercraft with payload of 2–3 tons is suitable for first-aid work in a disaster. The amount of load is appropriate for loading and unloading by manpower without using a special loading machine. Small loads with frequent return trip are desirable to fulfill needs that are changing from time to time. A system of first-aid transportation by a number of hovercraft of middle size is proposed in this paper as an additional system of transportation to existing ones. The system is very useful for first-aid transportation in a disaster.A simulation of hovercraft transportation was carried out after the Kobe Earthquake in 1995 as an example. We assume that 20 hovercraft of middle size are operated from 6 bases just outside of the disaster area to 12 destinations in the area. The result shows that they can transport up to 1,200 tons goods in a day in addition to those of conventional transportation means without disturbing them.     

Apparent Microfloral Response to Organic Degradation on Bathyal ­Seafloor: An Analysis Based on Sediment Fatty Acids

Abstract. Abyssal microfloral succession induced by experimental organic degradation was investigated. Notable changes in amounts and compositions of short-chain (C9-20) sediment fatty acids were observed, which indicated the shift of sediment microflora. Biomarker fatty acids for methanotrophs and sulfate-reducing bacteria dominated. Resultant fatty acid compositions were most closely related to those from a nearby methane seep harboring a dense Calyptogena colony; the clams were also seen in close vicinity of the deployed organic mass. These observations suggest that the organic degradation on the bathyal seafloor stimulates the formation of methanotrophic and thio­trophic microflora, resulting in the formation of a methane-seep-type benthic community.     

Infrared spectra of high-pressure hydrous silicates in the system MgO-SiO2-H2O

Infrared absorption spectra are presented for four hydrous magnesian silicates which are stable at high pressures and high temperatures characteristic of the earth's mantle: phase A (Mg₇Si₂O₁₄H₆), phase B (approx. Mg₂₃Si₈O₄₂H₆), chondrodite (Mg₅Si₂O₁₀H₂), clinohumite (Mg₉Si₄O₁₈H₂). The results show that phase B as well as phase A, chondrodite and clinohumite contain hydroxyl groups in their structures. It is also suggested that phase B, in addition to phase A, could be of potential importance in the upper mantle and transition zone as a dense host mineral for hydroxyl ions. Chemical composition of phase A was reexamined by microprobe analysis: it agrees well with Mg₇Si₂O₁₄H₆, estimated by Yamamoto and Akimoto (1974, 1977), but disagrees with a newly proposed formula Mg₂SiO₅H₂ by Benimoff and Sclar (1984).     

The system Mg2SiO4MgOH2O at high pressures and temperatures — Possible hydrous magnesian silicates in the mantle transition zone

The system Mg₂SiO₄MgOH₂O was investigated at pressures between 85 and 160 kbar and at temperatures between 750 and 1200°C. In runs for a gel with Mg/Si ratio of 3 and with 4.0 wt.-percent H₂O, a dense hydrous magnesian silicate, denoted phase B by Ringwood and Major, was found at pressures from about 100 kbar to at least 160 kbar in the whole temperature range studied. In the following table the crystallographic parameters and chemical formula of phase B, determined in this study, are compared with those of the other dense hydrous silicates in Mg₂SiO₄MgOH₂O.

     

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Phase	Composition	Space group	Cell parameters				Density (g cm?3)
			$\text{a}$	$\text{b}$	$\text{c}$	β
			(Å)	(Å)	(Å)	(°)
Chondrodite	Mg5Si2O10H2	$\text{P2}{}_1\text{/c}$	7.914	4.752	10.350	108.71	3.06
Clinohumite	Mg9Si4O18H2	$\text{P2}{}_1\text{/c}$	13.695	4.747	10.284	100.64	3.14
Phase A	Mg7Si2O14H6	$\text{P6}{}_3$	7.860		9.573		2.96
Phase B	Mg23Si8O42H6	$\text{P2}{}_1\text{/c}$	10.600	14.098	10.092	104.05	3.32