Carbonate deposits on submerged seamounts in the northwestern Pacific Ocean

Abstract   The lithology of shallow-water carbonates collected from 19 sites on 16 seamounts in six areas of the northwestern Pacific Ocean using the Deep-sea Boring Machine System are described. The areas include the Amami Plateau, Daito Ridge, Oki-Daito Ridge, Urdaneta Plateau, Kyushu-Palau Ridge and Ogasawara Plateau. Chronological constraint is provided by calcareous nannofossil biostratigraphy, planktonic foraminiferal biostratigraphy, larger foraminiferal biostratigraphy and strontium (Sr) isotope stratigraphy. Large amounts of shallow-water carbonates accumulated on the seamounts during the Oligocene, a relatively cool period, whereas limited carbonate deposits formed during the Early Miocene, a relatively warm period. This might indicate that deposition of shallow-water carbonates on seamounts in the northwestern Pacific Ocean was not necessarily controlled by climatic conditions, but was related to volcanism and tectonics that served as foundations for reef/carbonate-platform formation. Remarkable differences in biotic composition exist between Cretaceous and Cenozoic shallow-water carbonates. Late Cretaceous shallow-water carbonates are distinguished by the occurrence of rudists, solenoporacean algae and microencrusters. Middle Eocene to Early Oligocene shallow-water carbonates are dominated by Halimeda or nummulitid and discocyclinid larger foraminifers. Scleractinian corals became common from the Oligocene onward. Nongeniculate coralline algae and larger foraminifers were common to abundant throughout the Eocene to the Pleistocene. The replacement of major carbonate producers in the shallow-water carbonate factory during post-Cretaceous time is in accordance with previous studies and is considered to reflect a shift in seawater chemistry.     

Lunar photometric properties at wavelengths 0.5-1.6 μm acquired by SELENE Spectral Profiler and their dependency on local albedo and latitudinal zones

The lunar photometric function, which describes the dependency of the observed radiance on the observation geometry, is used for photometric correction of lunar visible/near-infrared data. A precise photometric correction parameter set is crucial for many applications including mineral identification and reflectance map mosaics. We present, for the first time, spectrally continuous photometric correction parameters for both sides of the Moon for wavelengths in the range 0.5-1.6 μm and solar phase angles between 5° and 85°, derived from Kaguya (SELENE) Spectral Profiler (SP) data. Since the measured radiance also depends on the surface albedo, we developed a statistical method for selecting areas with relatively uniform albedos from a nearly 7000-orbit SP data set. Using the selected data set, we obtained empirical photometric correction parameter sets for three albedo groups (high, medium, and low). We did this because the photometric function depends on the albedo, especially at phase angles below about 20° for which the shadow hiding opposition effect is appreciable. We determined the parameters in 160 bands and discovered a small variation in the opposition effect due to the albedo variation of mafic mineral absorption. The consistency of the photometric correction was checked by comparing observations made at different times of the same area on the lunar surface. Variations in the spectra obtained were lower than 2%, except for the large phase angle data in mare. Lastly, we developed a correction method for low solar elevation data, which is required for high latitude regions. By investigating low solar elevation data, we introduced an additional correction method. We used the new photometric correction to generate a 1° mesh global lunar reflectance map cube in a wavelength range of 0.5-1.6 μm. Surprisingly, these maps reveal that high latitude (?75°) regions in both the north and south have much lower spectral continuum slopes (color ratio r_1547.7nm/r_752.8nm ? 1.8) than the low and medium latitude regions, which implies lower degrees of space weathering.     

Correcting the Smoothing Effect of Ordinary Kriging Estimates

The smoothing effect of ordinary kriging is a well-known dangerous effect associated with this estimation technique. Consequently kriging estimates do not reproduce both histogram and semivariogram model of sample data. A four-step procedure for correcting the smoothing effect of ordinary kriging estimates is shown to be efficient for the reproduction of histogram and semivariogram without loss of local accuracy. Furthermore, this procedure provides a unique map sharing both local and global accuracies. Ordinary kriging with a proper correction for smoothing effect can be revitalized as a reliable estimation method that allows a better use of the available information.     

Subaqueous eruption and emplacement of the Shinjima Pumice, Shinjima (Moeshima) Island, Kagoshima Bay, SW Japan

The Shinjima Pumice is a fines-depleted pumice lapilli tuff emplaced several thousands years ago at about 100–140 m below sea level. This 40-m-thick deposit comprises many poorly defined flow units, which are 1–10 m thick, diffusely stratified and showing upward-coarsening of pumice clasts with a sharp to transitional base. Parallel to wavy diffuse stratifications are commonly represented by alignment of pumice clasts, especially in the lower half of the flow units. Pumice clasts of block to coarse-lapilli size commonly have thermal-contraction cracks best developed on the surfaces, demonstrating that they were hot but cooled down to the ambient temperatures prior to their emplacement. These features are suggestive of the direct origin of the Shinjima Pumice from subaqueous eruptions. A theoretical consideration on the behavior of subaqueous eruption plumes and hot and cold pumice clasts suggests that subaqueous eruption plumes commonly collapse by turbulent mixing with the ambient water and are transformed into water-logged mass flows.     

Sedimentation of terrigenous red soils in coastal area adjacent to an estuary and coral reefs,the Okkubi River estuary,Okinawa Island,Japan

Sedimentation process of fine-grained terrigenous red soils was observed on the seafloor by coral reefs near an estuary using a paired mooring of turbidity meter and sediment trap or a mooring of sediment trap and current meter. Silty clays contained in the bottom calcareous sands were mainly resuspended and trapped in both surface and bottom layer traps, at noncatastrophic normal sedimentation periods. In addition, silty clays were supplied to this mooring site by inflowing river. Turbidity and the flux rate determined by sediment traps show certain relationship accompanied with the coefficient, which is changed by precipitation, current, and other conditions. Resuspension process caused by a typhoon was recorded as both core sequence of sediment trap and time-series data of bottom current. Maximum velocity of 49.5 cm/s was recorded from bottom currents resulting from the passing of attyphoon at the mooring site. A graded sand layer is interbedded in dark-gray, silty clay and considered to be a resuspended sediment resulting from the passing of the typhoon. Flux of the resuspended sediments by the typhoon was estimated from this core sequence and compared to the flux observed at the normal sedimentation.     

Raman spectra of methane hydrate up to 86 GPa

High-pressure Raman studies of methane hydrate were performed using a diamond anvil cell in the pressure range of 0.1–86 GPa at room temperature. Raman spectra of the methane molecules revealed that new softened intramolecular vibration mode of ν ₁ appeared at 17 GPa and that the splitting of vibration mode of ν ₃ occurred at 15 GPa. The appearance of these two modes indicates that an intermolecular attractive interaction increases between the methane molecules and the host water molecules and between the neighboring methane molecules. These interactions might result in the exceptional stability of a high-pressure structure, a filled ice Ih structure (FIIhS) for methane hydrate, up to 40 GPa. At 40 GPa, a clear change in the slope of the Raman shift versus pressure occurred, and above 40 GPa the Raman shift of the vibration modes increased monotonously up to 86 GPa. A previous XRD study showed that the FIIhS transformed into another new high-pressure structure at 40 GPa. The change in the Raman spectra at 40 GPa may be induced by the transition of the structure.     

Nutricline shoaling in the eastern Pacific warm pool during the last two glacial maxima

Isoprenoid glycerol dialkyl glycerol tetraethers (GDGTs) and alkenones were analyzed in sediment samples retrieved from Ocean Drilling Program Site 1241 covering the last 150000 years to understand the hydrological evolution of the eastern Pacific warm pool (EPWP). GDGT and alkenone concentrations showed higher values in marine isotope stage (MIS)-2 and MIS-6, which suggests the enhancement of primary production at glacial maxima. $ {\text{TEX}}_{86}^{\text{H}} $ - and $ U_{ 3 7^\prime }^{\text{K}} $ -derived temperature depicted different temperature evolutions. $ U_{ 3 7^\prime }^{\text{K}} $ -derived temperature was marked by small variation during the glacial–interglacial cycles, whereas $ {\text{TEX}}_{86}^{\text{H}} $ -derived temperature showed pronounced glacial–interglacial variation that was similar to Mg/Ca-derived temperature records from nearby cores in the EPWP. Given that enhanced primary production during glacial maxima suggests nutricline shoaling, unchanged $ U_{ 3 7^\prime }^{\text{K}} $ over glacial–interglacial cycles can be interpreted as the shift of alkenone production depth. $ {\text{TEX}}_{86}^{\text{H}} $ seems not to be influenced by glacial–interglacial changes in nutricline depths, recording an integrated temperature in surface and thermocline water. The shallow nutricline in the EPWP during glacial maxima most likely reflected the intense formation of Antarctic intermediate water.     

The chemical composition and nickel,cobalt, copper,zinc and lead contents of Nanao Bay sediments

The contents of major and some of the minor elements, nickel, cobalt, copper, zinc and lead were studied on sediments collected from three inlets of Nanao Bay located at eastern side of Noto Peninsula. Little variation was found on the average contents of silicon, iron, titanium, aluminum, manganese, magnesium and potassium among the sediments of West, South and North Bays in Nanao Bay. Whereas significant difference was found on the contents of calcium, chlorine, sulfur and nitrogen among sediments of three bays.As to the minor elements, the average contents of nickel (20±5 ppm), cobalt (5±1 ppm), copper (18±5 ppm) and lead (17±8 ppm) are relatively low but zinc content is high in these sediments comparing with those of coastal deposit around Japan Island. From the results obtained here, it became clear that no environmental contamination of nickel, cobalt, copper and lead, and a little organic pollution were found in Nanao Bay sediments.