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.     

Petrology and geochemistry of prograde deserpentinized peridotites from Happo-O’ne, Japan: Evidence of element mobility during deserpentinization

The prograde deserpentinized peridotites from the talc zone in the Happo-O’ne complex, central Japan, show differences in their field relation and mineral assemblage with the high-P retrograde peridotites of the other part of the complex. They show a mineral assemblage, olivine + talc + antigorite ± prograde tremolite ± chlorite, formed by thermal metamorphism around the granitic intrusion at T, 500-650 °C and P < 7 kbar. The olivine has numerous opaque inclusions and high Fo (91.5-96.5) relative to the retrograde olivine, reflecting its formation by deserpentinization. The prograde tremolite, which is low in Al₂O₃ (<1.0 wt.%), Cr₂O₃ (<0.35 wt.%), and Na₂O (<0.6 wt.%) but high in Mg# (up to 0.98) and SiO₂ (up to 59.9 wt.%), is different in size, shape and chemistry from the retrograde tremolite. The prograde peridotites display a U-shaped REE pattern (0.02-0.5 times PM), similar to diopside-zone retrograde metaperidotites, possible protoliths. They are enriched in LILE (e.g., Cs, Pb, Sr, Rb) relative to HFSE (e.g., Ta, Hf, Zr, Nb), like their protoliths, because of their local re-equilibration with the fluid released during dehydration of the protoliths. They have high contents of REE and some trace elements (e.g., Cs, Th, U, Ta) relative to their protoliths because of an external-element addition from the granitic magma. In-situ analyses of peridotitic silicates confirmed that the prograde tremolite and talc display a spoon-shaped primitive mantle (PM)-normalized REE pattern (0.1-3 times PM) in which LREE are higher than HREE contents. The prograde tremolite is depleted in Al, Na, Cr, Sc, V, Ti, B, HREE and Li, but is enriched in Si, Cs, U, Th, HFSE (Hf, Zr, Nb, Ta), Rb and Ba relative to the retrograde tremolite; the immobile-element depletion in this tremolite is inherited from its source (antigorite + secondary diopside), whereas the depletion of mobile elements (e.g., Li, B, Na, Al) is ascribed to their mobility during the deserpentinization and/or the depleted character of the source of tremolite. The enrichment of HFSE and LILE in the prograde tremolite is related to an external addition of these elements from fluid/melt of the surrounding granitic magma and/or in situ equilibrium with LILE-bearing fluid released during dehydration of serpentinized retrograde metaperidotites and olivine-bearing serpentinites (protoliths). The prograde olivine is higher in REE and most trace-element contents than the retrograde one due to the external addition of these elements; it is enriched in B, Co and Ni, but depleted in Li that was liberated during deserpentinization by prograde metamorphism.     

Statistical empirical index of chemical weathering in igneous rocks: A new tool for evaluating the degree of weathering

Chemical weathering indices are useful tools in characterizing weathering profiles and determining the extent of weathering. However, the predictive performance of the conventional indices is critically dependent on the composition of the unweathered parent rock. To overcome this limitation, the present paper introduces an alternative statistical empirical index of chemical weathering that is extracted by the principal component analysis (PCA) of a large dataset derived from unweathered igneous rocks and their weathering profiles. The PCA analysis yields two principal components (PC1 and PC2), which capture 39.23% and 35.17% of total variability, respectively. The extent of weathering is reflected by variation along PC1, primarily due to the loss of Na₂O and CaO during weathering. In contrast, PC2 is the direction along which the projections of unweathered felsic, intermediate and mafic igneous rocks appear to be best discriminated; therefore, PC1 and PC2 represent independent latent variables that correspond to the extent of weathering and the chemistry of the unweathered parent rock. Subsequently, PC1 and PC2 were then mapped onto a ternary diagram (MFW diagram). The M and F vertices characterize mafic and felsic rock source, respectively, while the W vertex identifies the degree of weathering of these sources, independent of the chemistry of the unweathered parent rock.

The W index has a number of significant properties that are not found in conventional weathering indices. First, the W index is sensitive to chemical changes that occur during weathering because it is based on eight major oxides, whereas most conventional indices are defined by between two and four oxides. Second, the W index provides robust results even for highly weathered sesquioxide-rich samples. Third, the W index is applicable to a wide range of felsic, intermediate and mafic igneous rock types. Finally, the MFW diagram is expected to facilitate provenance analysis of sedimentary rocks by identifying their weathering trends and thereby enabling a backward estimate of the composition of the unweathered source rock.     

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.     

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.     

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.     

Platinum-group elements distribution and spinel composition in podiform chromitites and associated rocks from the upper mantle section of the Neoproterozoic Bou Azzer ophiolite, Anti-Atlas, Morocco

The distribution of platinum-group elements (PGEs), together with spinel composition, of podiform chromitites and serpentinized peridotites were examined to elucidate the nature of the upper mantle of the Neoproterozoic Bou Azzer ophiolite, Anti-Atlas, Morocco. The mantle section is dominated by harzburgite with less abundant dunite. Chromitite pods are also found as small lenses not exceeding a few meters in size. Almost all primary silicates have been altered, and chromian spinel is the only primary mineral that survived alteration. Chromian spinel of chromitites is less affected by hydrothermal alteration than that of mantle peridotites. All chromitite samples of the Bou Azzer ophiolite display a steep negative slope of PGE spidergrams, being enriched in Os, Ir and Ru, and extremely depleted in Pt and Pd. Harzburgites and dunites usually have intermediate to low PGE contents showing more or less unfractionated PGE patterns with conspicuous positive anomalies of Ru and Rh. Two types of magnetite veins in serpentinized peridotite, type I (fibrous) and type II (octahedral), have relatively low PGE contents, displaying a generally positive slope from Os to Pd in the former type, and positive slope from Os to Rh then negative from Rh to Pd in the latter type. These magnetite patterns demonstrate their early and late hydrothermal origin, respectively. Chromian spinel composition of chromitites, dunites and harzburgites reflects their highly depleted nature with little variations; the Cr# is, on average, 0.71, 0.68 and 0.71, respectively. The TiO₂ content is extremely low in chromian spinels, <0.10, of all rock types. The strong PGE fractionation of podiform chromitites and the high-Cr, low-Ti character of spinel of all rock types imply that the chromitites of the Bou Azzer ophiolite were formed either from a high-degree partial melting of primitive mantle, or from melting of already depleted mantle peridotites. This kind of melting is most easily accomplished in the supra-subduction zone environment, indicating a genetic link with supra-subduction zone magma, such as high-Mg andesite or arc tholeiite. This is a general feature in the Neoproterozoic upper mantle.