Interannual and synoptic-scale features of two types of cold-air outbreaks over the East China Sea during 1988�C2006

For the 1988?C2006 cold seasons, we investigated the characteristic structures of two types of cold-air outbreaks over the East China Sea: Type N, for which a thick layer of northerly meridional wind was formed during the cold-air outbreak; and Type S, for which an initially thin layer of northerly meridional wind was gradually thickened as the cold-air outbreak developed. The emergence frequencies of Type N and Type S outbreaks are sensitive to winter monsoon intensity at the 500-hectopascal (hPa) level. Type S outbreaks are dominant during strong El Ni?o events, leading to enhanced southerly meridional flow at 500?hPa over the East China Sea. The development of the 500-hPa Pacific High strongly influences the synoptic-scale structures of the two different types of outbreaks over the East China Sea.     

Bioaccumulation of nitroarenes in bivalves at Osaka Bay, Japan

This paper reports for the first time the detection and occurrence of nitroarenes (NPAHs) in marine organisms. Mussels and oysters collected from Osaka Bay, Japan, had total NPAHs concentrations that ranged from 2380 to 24,688 pg/g dry and 2672 to 25,961 pg/g dry, respectively. Relatively higher concentrations were detected in sampling sites located near the central district and suburbs of Osaka City implying that the most probable sources of NPAHs in the two bivalves are exhaust gases and smokes emitted by automobiles and industrial plants. Bivalves had relatively higher residues of 1-nitronaphthalene, 2-nitronaphthalene, 3-nitrophenanthrene, and 9-nitrophenanthrenes. Residues of 2-nitrofluorene, 1-nitropyrene, 4-nitropyrenes, and 6-nitrochrysene were much lower compared to nitronaphthalenes and nitrophenanthrenes. Inter-species differences was only observed for 2-nitronaphthalene with oysters exhibiting significantly higher residues than mussels.     

Japan’s Nation-Wide Electronic Geotechnical Database Systems by Japanese Geotechnical Society

On October 15, 2010, the Japanese Geotechnical Society (JGS) announced the public release of ‘Nation-wide Electronic Geotechnical Database Systems,’ which provides geotechnical information to the public on the internet. The information the system provides is a collection of ground models at 250 m by 250 m in plan built by using data from various geotechnical information databases. The paper first describes historical development of the geotechnical information databases in Japan, and introduces a 5-year project, ‘Integrated Geophysical and Geological Information Database in Japan,’ led by the National Research Institute for Earth Science and Disaster Prevention (NIED), and participated by the JGS. The paper then presents the JGS’ ‘Nation-wide Electronic Geotechnical Database Systems,’ and describes why such system was proposed and built, followed by the presentation of the examples for possible application of the system.     

Geochemical analyses of geological layers and groundwater flows

X-ray fluorescent spectroscope analysis easily finds ratios of geochemical elements in soil. Applying the method of ratio matching to measured ratios, the classification of geological layers, and the flow directions of groundwater can be determined. This method is applied to three hill slopes in Japan and the results are in good agreement with the observations and measurements of soil cores obtained by drilling. The classification of geological layers is found to be quantitatively connected with the rates of organic matter in soil cores. Received: 5 February 1999 · Accepted: 7 September 1999     

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.     

Mesoscale structures of two types of cold-air outbreaks over the East China Sea and the effect of coastal sea surface temperature

Two types of cold-air outbreaks over the Yellow and East China Seas are investigated using a regional mesoscale model. Distinct patterns of surface turbulent heat fluxes and precipitation are identified between the two cases. The sea surface heat flux and frictional velocity are strongly influenced by mesoscale differences between high- and low-resolution datasets of sea surface temperature (SST). The influence of the SST difference on atmospheric water is spread to the downstream area of the outbreak with the phase transition of water. The air mass transformation around 800?hPa over the Kuroshio is partly influenced by the upstream SST difference. In particular, the SST difference near the mouth of the Yanzi River strongly modifies the air mass around Taiwan. Thus, in addition to the Kuroshio front, the mesoscale Chinese coastal SST structure is also important in the air mass transformation over the East China Sea.     

Ore mineralogy and sulfur isotope study of the massive sulfide deposit of Filon Norte,Tharsis Mine,Spain

The volcanogenic massive sulfide deposit of Filon Norte at Tharsis is hosted by carbonaceous black slate and connected only partly with stockwork veins. The massive ores are usually composed of fine-grained pyrite with subordinate amounts of sphalerite, chalcopyrite, galena and arsenopyrite. Monoclinic pyrrhotite sometimes occurs in massive pyritic ores in the apparently middle and upper horizons of the orebody, and siderite-rich ores are interstratified with compact pyritic ores in the apparently lower horizons. From the occurrence of monoclinic pyrrhotite, together with the FeS contents of sphalerite mostly ranging from 11 to 16 mol %, it is inferred that the sulfide minerals of the massive orebody were precipitated in euxinic muds on the sea-floor at temperatures below 250°C. The negatively shifted, highly variable ³⁴S values of the massive ores and their close similarity to those of the underlying black slates strongly suggest that the sulfide sulfur of the massive orebody and the slates is cognate and biogenic.     

Interstellar cyanomethane

We have made an observational study of the newly identified cyanomethane radical CH2CN and the possibly related species CH3CN with the goals of (1) elucidating the possible role of reactions of the type CnHm(+) + N in astrochemistry, and (2) providing a possible test of Bates's models of dissociative electron recombination. We find a remarkably different abundance ratio CH2CN/CH3CN in TMC-1 and Sgr B2, which we deduce is a result of the large difference in temperature of these objects. Studies of CH2CN and CH3CN in other sources, including two new detections of CH2CN, support this conclusion and are consistent with a monotonic increase in the CH2CN/CH3CN ratio with decreasing temperature over the range 10-120 K. This behavior may be explained by the destruction of CH2CN by reaction with O. If this reaction does not proceed, then CH2CN and CH3CN are concluded to form via different chemical pathways. Thus, they do not provide a test of Bates's conjectures (they do not both form from CH3CNH+). CH2CN is then likely to form via C2H4(+) + N --> CH2CNH+, thus demonstrating the viability of this important reaction in astrochemistry. The T dependence of the CH2CN/CH3CN ratio would then reflect the increasing rate of the C2H4(+) + N reaction with decreasing temperature.