A comparison of methods for calculating the motion of a semi-submersible

The 17th ITTC Ocean Engineering Committee undertook the comparison of methods for calculating semi-submersible wave motion, and 34 programs from 28 different organizations participated in the project. The summary of the results are reported in the Technical Report of the 17th ITTC (ITTC, 1984).In this paper, the details of the project are described. Namely, almost all the calculation results of the 34 programs are shown and examined from the viewpoints of the validity of the program itself and of the correlation between the differences in the various calculation methods and the differences in the calculation results. The calculation results are also compared with the experiments, the details of which are also illustrated.     

Petrological feature of spinel lherzolite xenolith from Oki-Dogo Island: An implication for variety of the upper mantle peridotite beneath southwestern Japan

Abstract   Spinel lherzolite is a minor component of the deep-seated xenolith suite in the Oki-Dogo alkaline basalts, whereas other types of ultramafic (e.g. pyroxenite and dunite) and mafic (e.g. granulite and gabbro) xenoliths are abundant. All spinel lherzolite xenoliths have spinel with a low Cr number (Cr#; < 0.26). They are anhydrous and are free of modal metasomatism. Their mineral assemblages and microtextures, combined with the high NiO content in olivine, suggest that they are of residual origin. But the Mg numbers of silicate minerals are lower (e.g. down to Fo₈₆) in some spinel lherzolites than in typical upper mantle residual peridotites. The clinopyroxene in the spinel lherzolite shows U-shaped chondrite-normalized rare-earth element (REE) patterns. The abundance of Fe-rich ultramafic and mafic cumulate xenoliths in Oki-Dogo alkali basalts suggests that the later formation of those Fe-rich cumulates from alkaline magma was the cause of Fe- and light REE (LREE)-enrichment in residual peridotite. The similar REE patterns are observed in spinel peridotite xenoliths from Kurose and also in those from the South-west Japan arc, which are non-metasomatized in terms of major-element chemistry (e.g. Fo > 89), and are rarely associated with Fe-rich cumulus mafic and ultramafic xenoliths. This indicates that the LREE-enrichment in mantle rocks has been more prominent and prevalent than Fe and other major-element enrichment during the metasomatism.     

The Nature of Mantle Rocks in Ophiolites of the Polar Urals

This work presents the results of geochemical (LA-ICP-MS) study of minerals of peridotites from ophiolite complexes of the Polar Urals to clarify the nature of these formations. The distribution of trace and rare earth elements in clinopyroxenes testifies that there were three types of the mantle substratum, which formed in different geodynamic settings. Two types of primary peridotites were formed upon partial melting of the mantle at different-depth levels in the subduction zone. The first type is represented by lherzolites and diopside harzburgites, formed at partial melting under the spinel facies conditions; the second type is represented by diopside harzburgites, formed under polybaric partial melting under the garnet and spinel facies conditions. In the suprasubduction zone, peridotites experienced fluid-induced partial melting that resulted in crystallization of harzburgites. All types of harzburgites were transformed by ascending melts and fluids (refertilization) and high-temperature hydration with the formation of amphibole. These processes are recorded in variations in the REE spectra of minerals.     

Characteristics of amorphous kerogens fractionated from terrigenous sedimentary rocks

A preliminary attempt to fractionate amorphous kerogens from terrigenous bulk kerogen by a benzene-water two phase partition method under acidic condition was made. Microscopic observation revealed that amorphous kerogens and structured kerogens were fractionated effectively by this method. Characteristics of the amorphous and structured kerogens fractionated by this method were examined by some chemical analyses and compared with those of the bulk kerogen and humic acid isolated from the same rock sample (Haizume Formation, Pleistocene, Japan). The elemental and infrared (IR) analyses showed that the amorphous kerogen fraction had the highest atomic$\text{H}\text{C}$ ratio and the lowest atomic $\text{N}\text{C}$ ratio and was the richest in aliphatic structures and carbonyl and carboxyl functional groups. Quantities of fatty acids from the saponification products of each geopolymer were in agreement with the results of elemental and IR analyses. Distribution of the fatty acids was suggestive that more animal lipids participate in the formation of amorphous kerogens because of the abundance of relatively lower molecular weight fatty acids (such as C₁₆ and C₁₈ acids) in saponification products of amorphous kerogens. On the other hand, although the amorphous kerogen fraction tends to be rich in aliphatic structures compared with bulk kerogen of the same rock samples, van Krevelen plots of elemental compositions of kerogens from the core samples (Nishiyama Oil Field, Tertiary, Japan) reveal that the amorphous kerogen fraction is not necessarily characterized by markedly high atomic $\text{H}\text{C}$ ratio. This was attributed to the oxic environment of deposition and the abundance of biodegraded terrestrial amorphous organic matter in the amorphous kerogen fraction used in this work.     

Field survey of the East Java earthquake and tsunami of June 3, 1994

A field survey of the June 3, 1994 East Java earthquake tsunami was conducted within three weeks, and the distributions of the seismic intensities, tsunami heights, and human and house damages were surveyed. The seismic intensities on the south coasts of Java and Bali Islands were small for an earthquake with magnitudeM 7.6. The earthquake caused no land damage. About 40 minutes after the main shock, a huge tsunami attacked the coasts, several villages in East Java Province were damaged severely, and 223 persons perished. At Pancer Village about 70 percent of the houses were swept away and 121 persons were killed by the tsunami. The relationship between tsunami heights and distances from the source shows that the Hatori's tsunami magnitude wasm=3, which seems to be larger for the earthquake magnitude. But we should not consider this an extraordinary event because it was pointed out byHatori (1994) that the magnitudes of tsunamis in the Indonesia-Philippine region generally exceed 1–2 grade larger than those of other regions.     

Trace element compositions of jadeite (+omphacite) in jadeitites from the Itoigawa-Ohmi district, Japan: Implications for fluid processes in subduction zones

Abstract   Trace-element compositions of jadeite (±omphacite) in jadeitites from the Itoigawa-Ohmi district of Japan, analyzed by a laser-ablation inductively coupled plasma mass spectrometry technique showed chemical zoning within individual grains and variations within each sample and between different samples. Primitive mantle-normalized patterns of jadeite in the samples generally showed high large-ion lithophile element contents, high light rare earth element/heavy rare earth element ratios and positive anomalies of high field strength elements. The studied jadeitites have no signatures of the protolith texture or mineralogy. Shapes and distributions of minerals coupled with chemical zoning within grains suggest that the jadeitites were formed by direct precipitation of minerals from aqueous fluids or complete metasomatic modification of the precursor rocks by fluids. In either case, the geochemical characteristics of jadeite are highly affected by fluids enriched in both large-ion lithophile elements and high field strength elements. The specific fluids responsible for the formation of jadeitites are related to serpentinization by slab-derived fluids in subduction zones. This process is followed by dissolving high field strength elements in the subducting crust as the fluids continue to circulate into the subducting crusts and serpentinized peridotites. The fluids have variations in chemical compositions corresponding to various degrees of water–rock interactions.