An Interactive Deformation System for Granular Material

Computer Graphics (CG) animations of natural phenomena are currently widely used for movies and in video games. Granular materials occur widely in nature, and therefore it is necessary that CG animations represent ground surfaces composed of a granular material as well as model deformations when the granular material comes into contact with other physical rigid objects (called solid objects). In this paper, we propose a deformation algorithm for ground surfaces composed of granular material. The deformation algorithm is divided into three steps: (1) detection of the collision between a solid object and the ground surface, (2) displacement of the granular material and (3) erosion of the material at steep slopes. The proposed algorithm can handle solid objects of various shapes, including concave polyhedra by additionally using a layered data structure called the Height Span Map. Furthermore, a texture sliding technique is presented to render the motion of granular materials. In addition, our implementation of the deformation algorithm can be used at interactive frame rates.     

Market micro-structure analysis by multiagent simulation in X-Economy -- comparison among technical indices

We are developing an agent and server library referred to as X-Economy, by which we can execute multiagent simulations and network games for financial and economic systems. To this end, we analyzed the characteristics of network games in a financial context and compared them with traditional ones. X-Economy has also provided a new research direction in market micro-structure analysis. We executed several kinds of multiagent simulations for technical traders (indices) and obtained non-trivial suggestions regarding the relationship between the market randomness and the effectiveness of technical indices. For instance, the performance of complex technical indices seemed to deeply depend on the characteristics and nature of a market when a market became complex, i.e. it moved far from the Wiener process.     

Light‐emitting polymers for full‐color display applications

The latest developments in light‐emitting‐polymer (LEP) technology at CDT continue to show steady progress. Device performance for blue, green, and red systems as well as a high‐performance yellow system in terms of device efficiency and stability will be described. Some of the issues associated with the commercialization of LEP technology including the development of direct‐patterning techniques enabling full‐color passive‐ and active‐matrix display will be discussed.     

Time-frequency MEG-MUSIC algorithm

We propose a method that incorporates the time-frequency characteristics of neural sources into magnetoencephalographic (MEG) source estimation. The method is based on the multiple-signal-classification (MUSIC) algorithm and it calculates a time--frequency matrix in which diagonal and off-diagonal terms are the auto and crosstime--frequency distributions of multichannel MEG recordings, respectively. The method averages this time-frequency matrix over the time--frequency region of interest. The locations of neural sources are then estimated by checking the orthogonality between the noise subspace of this averaged matrix and the sensor lead field. Accordingly, the method allows us to estimate the locations of neural sources from each time--frequency component. A computer simulation was performed to test the validity of the proposed method, and the results demonstrate its effectiveness.     

Synthesis and Physical Properties of (Cu,M)Ba2Ca3Cu4Oz (M=C,Mg,Ni,Al,Zn,Tl)

We have synthesized the single phase samples of Cu _x C _0.1 Ba ₂ Ca ₃ Cu ₄ O _z (x=0.20.9). Transport and magnetic measurements and iodometric titration analysis were carried out for these materials. From these results we discuss the correlation between T _c , the Hall number, copper valence and oxygen content. The effect of the substituted M ions on T _c in (CuC, M)-l234 (M=Ni,Zn,Al,TI,Mg) is also discussed. We propose a unique selective carrier-doping mechanism in (Cu,C)- and (CuC,Mg)-1234 systems.     

Heat and mass transfer during crystal growth

Quality of semiconductor and oxide crystals which are grown from the melts plays an important role for electronic and/or optical devices. The crystal quality is significantly affected by the heat and mass transfer in the melts during crystal growth in a growth furnace such as Czochralski or horizontal Bridgman methods. This paper reviews the present understanding of phenomena of the heat and mass transfer of the melts, especially instability of melt convection from the detailed numerical calculation, which helps to understand the melt convection visualized using X-ray radiography. Large scale simulation of melt convection during crystal growth is also reviewed.

Characteristics of flow instabilities of melt convection with a low Prandtl number (ratio between momentum and thermal diffusivities) are also reviewed by focusing on the instabilities of baroclinic, the Rayleigh-Benard and the Marangoni-Benard, from the points of view of temperature, rotating and/or magnetic field effects during crystal growth. Oxygen concentration in grown crystals is also discussed how melt convection affects.     

Wideband optical transmission in smectic liquid crystal lightmodulator at room temperature

Video rate optical transmission at room temperature (RT) for smectic liquid crystal light modulators (SLCLMs) and filter circuits has been demonstrated. The bandwidth of this system has been determined to be 5.6 MHz. Optical transmission of the National Television System Committee (NTSC) video signal at RT has been realised     

Structures of spider toxins: hydroxyindole-3-acetylpolyamines and a new generalized structure of type-E compounds obtained from the venom of the Joro spider, Nephila clavata

Facile structure determination of acylpolyamines, glutamatergic nerve blocker obtained from the venom of the Joro spider (Nephila clavata) was carried out with the use of micro-column LC/MS and high energy collision induced dissociation (CID) mass spectrometry. 6-hydroxyindole-3-acetyl was proposed previously as a putative partial structure, for the acyl moiety of hydroxyindole-type polyamines (NPTX-1 to -6). The NMR data obtained for NPTX-6, NPTX-687 and hydroxyindole-3-acetic acid which was released by acid hydrolysis of Nephila clavata crude venom extracts proved that the lipophilic head is the 4-hydroxyindole-3-acetic acid. Various hydroxyindole-3-acetyl polyamines were found in N. Clavata venom and characterized by mass spectrometry. As a result, type-E, a new class of generalized acylpolyamine structure was proposed in addition to the previously reported polyamine backbones type-A to -D.     

Evidence against a direct role for the induction of c-jun expression in the mediation of drug-induced apoptosis in human acute leukemia cells

Previous reports have demonstrated that a variety of anticancer drugs, e.g., 1-beta-D-arabinofuranosylcytosine (ara-C), mitoxantrone, etoposide, camptothecin, and cisplatin, induce the expression of c-jun oncogene in leukemic cells prior to producing internucleosomal DNA fragmentation and the morphological features of apoptosis. This has led to the impression that the induction of c-jun expression may be directly involved in the molecular signaling of the final common pathway of programmed cell death or apoptosis. In the present study, we examined the role of c-jun expression in three different settings of anticancer drug-induced apoptosis in human leukemic cells. First, exposure of human myeloid leukemia HL-60 cells to high-dose ara-C for 4 h produced internucleosomal DNA fragmentation preceded by c-jun induction. However, pretreatment of HL-60 cells with staurosporine, a protein kinase C inhibitor, repressed c-jun yet enhanced DNA fragmentation and apoptosis due to ara-C. Second, in human pre-B leukemia 697/BCL-2 cells which are transfected with the cDNA of the bcl-2 oncogene and overexpress p26BCL-2, although ara-C or mitoxantrone treatment caused greater c-jun induction than in the 697/neo cells, significantly reduced endonucleolytic DNA fragmentation and apoptosis was observed in 697/BCL-2 cells. Finally, taxol-induced internucleosomal DNA fragmentation and morphological features of apoptosis in HL-60 cells were not associated with the induction of c-jun expression. These lines of evidence indicate that the induction of c-jun expression may not have a direct role in the molecular signaling of anticancer drug-induced apoptosis, and that the anticancer drug-induced apoptosis can occur by a mechanism that does not involve the induction of c-jun expression.