Phytoplankton communities in the Bering Sea and adjacent seas

Vertical distribution of phytoplankton in early warming season in the eastern Bering Sea and adjacent sea areas was investigated. In the surface layer which was under the influence of newly melted sea ice in the shelf water region of the Bering Sea in May, remarkably dense populations ofThalassiosira hyalina andT. nordenskiöldii and relatively large populations ofFragilaria andNavicula occupied large part of phytoplankton community. In June, although theThalassiosira populations sunk into the bottom layer and withered, a certain part of theFragilaria-Navicula populations was still suspended in subsurface layer. Thus,Fragilaria-Navicula were the leading components of the June community in the shelf region.In the Bering Basin region, no dense phytoplankton populations were developed until a shallow thermocline was established. In June when the shallow thermocline developed near shelf edge,Thalassiosira decipiens burst out. As the shallow thermocline extended from near shelf to central part of the Basin region with surface warming, the areas of blooming also shifted from near shelf to the central part.Contribution No. 73 from the Research Institute of North Pacific Fisheries, Hokkaido University.     

The distribution of manganese and iron between ilmenite and granitic magma in the Ôsumi Peninsula,Japan

Manganoan ilmenite with a variable manganese content occurs as an early accessory constituent of granitic rocks in the Ôsumi Peninsula, southern Kyushu. Electron probe micro-analysis of a grain containing highest manganese gives the structural formula (Fe _1.23 ²⁺ Mn _0.81 ²⁺ ) (Ti_1.97) O₆, if all of the manganese and iron are in the divalent state. The manganese content of manganoan ilmenite increases with an increase of the differentiation index of host rocks, however, the amount of ilmenite tends to decrease with the increase of the same index. The mode of occurrence of the ilmenite suggests that it is the first mafic mineral to precipitate from the magma. The average value of the distribution coefficient of manganese and ferrous iron between ilmenite and granitic magma is 5.5, if the Mn/Fe ratio of the granitic rocks represents that of granitic magma. The variation in the FeO and MnO contents against the differentiation index for granitic rocks of the Ôsumi Peninsula, and the value of the distribution coefficient, show that high manganoan ilmenite is stable in the most differentiated granitic rock of the Ôsumi Peninsula.     

Determination of Ge, As, Se and Te in Silicate Samples Using Isotope Dilution-Internal Standardisation Octopole Reaction Cell ICP-QMS by Normal Sample Nebulisation

A method for the determination of Ge, As, Se and Te in silicate samples using isotope dilution-internal standardisation (ID-IS) octopole reaction cell (ORC) ICP-QMS by normal sample nebulisation was developed. The method does not involve either hydride generation or ion exchange. Germanium, Se and Te were determined by isotope dilution (ID), and As was determined by ID-IS. A silicate sample with an added Ge-Se-Te spike was digested with an HF-HNO₃-HBr mixture, dried, re-dissolved with HF and the supernatant liquid was directly aspirated into an ORC-ICP-QMS instrument with He or H₂ gas. No matrix effects were observed down to a dilution factor (DF) of ∼ 70 for Ge, Se and Te and DF of ∼ 1000 for As, which resulted in 3s detection limits in silicates of 2, 1, 0.1 and 4 ng g⁻¹, respectively. Advantages of the method are the simple sample introduction as well as a capability of determining S, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta by ID-IS-ICP-QMS/SFMS from the same solution. Furthermore, the total sample solution consumption was only 0.253 ml with DF = 2000. Therefore, only a 0.13 mg test portion was required. To demonstrate the applicability of this technique, Ge, As, Se and Te in eight silicate reference materials were determined, as well as S, Ti, Zr, Nb, Mo, Sn, Sb, Hf and Ta in four carbonaceous chondrites.     

Viscosity of peridotite liquid up to 13 GPa: Implications for magma ocean viscosities

The viscosity of synthetic peridotite liquid has been investigated at high pressures using in-situ falling sphere viscometry by combining a multi-anvil technique with synchrotron radiation. We used a newly designed capsule containing a small recessed reservoir outside of the hot spot of the heater, in which a viscosity marker sphere is embedded in a forsterite + enstatite mixture having a higher solidus temperature than the peridotite. This experimental setup prevents spheres from falling before a stable temperature above the liquidus is established and thus avoids difficulties in evaluating viscosities from velocities of spheres falling through a partially molten sample.

Experiments have been performed between 2.8 and 13 GPa at temperatures ranging from 2043 to 2523 K. Measured viscosities range from 0.019 (± 0.004) to 0.13 (± 0.02) Pa s. At constant temperature, viscosity increases with increasing pressure up to  8.5 GPa but then decreases between  8.5 and 13 GPa. The change in the pressure dependence of viscosity is likely associated with structural changes of the liquid that occur upon compression. By combining our results with recently published 0.1 MPa peridotite liquid viscosities [D.B. Dingwell, C. Courtial, D. Giordano, A. Nichols, Viscosity of peridotite liquid, Earth Planet. Sci. Lett. 226 (2004) 127–138.], the experimental data can be described by a non-Arrhenian, empirical Vogel-Fulcher-Tamman equation, which has been modified by adding a term to account for the observed pressure dependence of viscosity. This equation reproduces measured viscosities to within 0.08 log₁₀-units on average. We use this model to calculate viscosities of a peridotitic magma ocean along a liquid adiabat to a depth of  400 km and discuss possible effects on viscosity at greater pressures and temperatures than experimentally investigated.     

Spatial partitioning between species of the phytoplankton-feeding guild on an estuarine intertidal sand flat and its implication on habitat carrying capacity

The fishery yield of Manila clams, Ruditapes philippinarum, increased considerably in the 1970s but has decreased rapidly since the middle 1980s on extensive intertidal sand flats in Ariake Sound (Kyushu, Japan). A survey conducted in 2004 on a 3.4-km² sand flat located in the central part of the Sound (Shirakawa sand flat) revealed four dominant species: two thalassinidean shrimps (Upogebia major and Nihonotrypaea japonica), which are deep-reaching burrow dwellers with strong bioturbation activities, and two bivalves (Mactra veneriformis and R. philippinarum). All four species belong to a phytoplankton (diatom)-feeding guild. In the late 1970s, the Manila clam population prevailed in high densities over the entire sand flat, whereas its distribution was restricted to the lowest quarter of the shore in 2004. In contrast, the population sizes and zones of occurrence of the other phytoplankton feeders have expanded in the absence of R. philippinarum, perhaps an indication of competitive release. After establishment, effects of the thalassinidean shrimps on sediment stability appear to have further reduced clam abundances. Across the sand flat in 2004, wet weight population biomass estimates for N. japonica, U. major, M. veneriformis, and R. philippinarum (whole body for shrimps and soft tissue for bivalves) were 304, 111, 378, and 234 tonnes, respectively. Based on Manila clam fishery yield records from Shirakawa, the carrying capacity of the Shirakawa sand flat in the late 1970s was estimated to be two times greater than the sum value for the whole phytoplankton-feeding guild in 2004. It is hypothesized that (1) the amount of phytoplankton determines the carrying capacity for the benthic community on the Shirakawa sand flat, with both phytoplankton and benthic biomass at maxima in the late 1970s, and (2) the subsequent increases in competition for space have caused further declines in the Manila clam population biomass to approximately one-eighth of its past value.     

Fine structure beneath the Tohoku district, northeastern Japan arc, as derived by an inversion of P-wave arrival times from local earthquakes

Three dimensional P-wave velocity structure beneath the Tohoku district, northeastern Japan arc, is investigated by an inversion of arrival times from local earthquakes using the method originally due to Aki and Lee (1976).In the crust (0–32 km depth) a low-velocity region is found along the volcanic front and its vicinity. Velocities at depths of 32–65 km are low beneath the regions where many Quaternary volcanoes and geothermal areas are distributed. In the region deeper than 65 km, the subduction of the Pacific plate is clearly revealed, and the mantle structure above the descending plate is rather uniform. These features suggest that volcanic activities have relation to the upper mantle structure. The results obtained in this study will be helpful in investigating the mechanism of magma generation in a subduction zone.     

Fracture strength of dry silicate rocks at high confining pressures and activity of acoustic emission

Three dry silicate rocks, gabbro, dunite and eclogite, were triaxially compressed up to a confining pressure of 3 GPa at room temperature. These rocks exhibited brittle fracture behavior up to the highest confining pressure. The change of the mechanism of fracture in the brittle region is suggested from the measurement of the compressive fracture strength and the activity of acoustic emission. The existence of the “high-pressure brittle-fracture” phase is proposed. The fracture strength increased with increase of confining pressure. The increasing rate of strength was lowered at a value of confining pressure: at about 0.8 GPa on gabbro; at about 1.0 GPa on dunite; and at about 1.5 GPa on eclogite. At lower confining pressures than the above value, the acoustic emission rate began to increase at the onset of dilatancy and increased rapidly followed by fracture as the axial stress was increased. At the higher confining pressures, however, the acoustic emission rate did not increase rapidly before final fracture, and stayed constant to the fracture. The similar behavior was shown on the granite studied previously. It is interesting that the frictional strength forms the boundary between “low- and high-pressure brittle-fracture” phases.     

Determination of Zirconium, Niobium, Hafnium and Tantalum at ng g-1 Levels in Geological Materials by Direct Nebulisation of Sample HF Solution into FI-ICP-MS

We have developed a rapid and accurate method to determine Zr, Nb, Hf and Ta (denoted as HFSE) in geological samples by inductively coupled plasma-mass spectrometry fitted with a flow injection system (FI-ICP-MS). The method involves sample decomposition by HF followed by HF dissolution of HFSE coprecipitated with insoluble M and Ca fluoride residues formed during the initial HF attack. This HF solution was directly nebulized into an ICP mass spectrometer. An external calibration curve method and an isotope dilution method (ID) were applied for the determination of Nb and Ta, and of Zr and Hf, respectively. Recovery yields of HFSE were > 96% for peridotite, basalt and andesite compositions, apart from Zr and Hf for peridotite (> 85%). No matrix effects for either signal intensities of HFSE or isotope ratios of Zr and Hf were observed in basalt, andesite and peridotite solutions down to a dilution factor of 100. Detection limits in silicate rocks were 40, 2, 1 and 0.1 ng g-1 for Zr, Nb, Hf and Ta, respectively. This technique required only 0.1 ml of sample solution, and thus is suitable for analysing small and/or precious samples such as meteorites, mantle peridotites and their mineral separates. We also present newly determined data for the Zr, Nb, Hf and Ta concentrations in USGS silicate reference materials DTS-1, PCC-1, BCR-1, BHVO-1 and AGV-1, GSJ reference materials JB-1, -2, -3, JA-1, -2 and -3, and the Smithsonian reference Allende powder.     

Determination of Molybdenum, Antimony and Tungsten at sub μg g−1 Levels in Geological Materials by ID-FI-ICP-MS

We have developed a rapid and accurate method for the determination of Mo, Sb and W in geological samples using isotope dilution inductively coupled plasma-mass spectrometry with a flow injection system (ID-FI-ICP-MS). The chemical procedure requires HF digestion of the sample with a Mo-Sb-W mixed spike, subsequent evaporation and dissolution of Mo, Sb and W from Mg and Ca fluorides with HF. Recovery yields of Mo, Sb and W in the extraction were > 94% for samples of peridotite, basalt and andesite composition, with the exception of W in samples of peridotite composition for which recovery was 81%. No matrix effects were observed in the determination of the isotope ratios of Mo, Sb and W in solutions prepared from peridotite, basalt and andesite samples down to a dilution factor of 100. Detection limits of Mo, Sb and W in silicate materials were at the several ng g⁻¹ level. Analysis of the silicate reference materials PCC-1, DTS-1, BCR-1, BHVO-1, AGV-1 from the US Geological Survey and JP-1, JB-1, -2, -3, JA-1, -2, and -3 from the Geological Survey of Japan as well as the Smithsonian reference Allende powder yielded reliable Mo, Sb and W concentrations. The repeatability in the analysis of basalts and andesites was < 9%. This technique requires only 0.2 ml sample solution, and is therefore suitable for analyzing small and/or precious samples such as meteorites, mantle peridotites and their mineral separates.