Numerical study of transverse lattice waves connected with martensitic transformation

The behavior of the transverse lattice wave connected with the nucleation process of martensite is studied, taking into account the anharmonicity, by use of one-dimensional model for the crystal. The key factor which determines the behavior of the transverse lattice waves according to the model is its amplitudeA with respect to the critical amplitudeA _c. As far asA < A _c, the presence of the transverse lattice wave does not lead to the initiation of the martensite. Depending on the variation ofA andA _c with temperature, the model suggests two alternative processes for the initiation of the martensitic transformation. 1) In case the variation ofA _c with temperature is larger than the variation ofA with temperature, the transverse lattice wave develops into the stable nuclei of the martensite, as soon asA _c becomes smaller thanA with decrease of temperature. 2) In case the variation ofA with temperature is larger than the variation ofA _c with temperature, the transverse lattice wave represents the heterophase fluctuation whenA « A _c. The stable martensite is formed with the reduction ofA as temperature is reduced. The presently available experimental data suggest the process 1) as the nucleation mechanism of the martensite. The prominent role of the interface energy between the martensite and the austenite in determining both the structure of the martensite and the dispersion relationship of the transverse lattice wave in the austenite is pointed out.     

The effect of excess gate current on input impedance of a JFET amplifier

When JFET is used as an amplifier, it should be regarded that the effect of excess gate current on the input impedance is changed by gain of the amplifier. The input impedance or conductance with gain of the JFET amplifier is experimentally analyzed applying small signal equivalent circuit.     

Successfully operated case of posterior fossa tuberculoma in childhood (author's transl)

A case of intracerebellar tuberculoma is described in which a tuberculoma was removed successfully through the administration of antituberculous agents, and a full recovery was obtained. The patient was a 3-year-old boy who had been receiving antituberculous agents for about 4 months because of acute inflammation followed by osteomyelitis of his right big toe, which was suspected to be tuberculous, and because of pulmonary tuberculosis diagnosed in a chest roentgenogram taken about 1 month after osteomyelitis was cured. While his osteomyelitis was being treated, disturbance in his gait, due to progressive spastic paraparesis, was not iced, and thereafter left cerebellar symptoms with impairment of equilibrium appeared additionally. Then, he was reffered to our clinic for further neurosurgical examination, and was admitted on November 1, 1974 after right carotid and vertebral angiography was performed via the right axillar artery, in which findings suggesting left cerebellar tumor and internal hydrocephalus were obtained. After he was admitted to our clinic, a diagnosis of tumor of the left cerebellum and internal hydrocephalus was more precisely confirmed by pneumoventriculography. Suboccipital craniectomy was then carried out and the tumor, weighing 60 gm, was completely removed from the left cerbellar hemisphere. The tumor was confirmed as tuberculoma not only by histological findings but also by the vertification of tuberculous bacilli in it. Though, moderate fever lasted for about 2 weeks postoperatively, no obvious meningitic signs or new neurological deficits were noted. The patient showed marked improvement especially in his gait disturbance, and was discharged ambulatory 40 days after the operation, and has since been asymptomatic except for slight ataxic gait. The antituberculous agents have been continuously administered postoperatively.     

Occurrence and determination of a herbicide benthiocarb in rivers and agricultural drainages

The occurrence and determination of a herbicide, benthiocarb, 4-chlorobenzyl N,N-diethylthiolcarbamate (Saturn^®) in rivers and agricultural drainages was investigated. Benthiocarb residues were detected in water samples when it has been applied to rice paddies, after rice seedling transplantation, in concentrations of between 10.00 and 0.11 μg/l. These residues entered into rivers and agricultural drainages as a result of overflows from rice paddies. However, benthiocarb residues could not be found in water samples after the termination of its application to rice paddies, suggesting that the applied benthiocarb might be degraded by microbial and physico-chemical actions such as photochemical reactions occurring on the soil surface. Benthiocarb residue levels were higher in longer rivers than in agricultural drainage. The contribution of rainfall to the benthiocarb concentrations was shown. Benthiocarb in water was extracted with n-hexane and identified by a gas chromatography using a flame photometric detector (sulphur filter 394 nm) and a combined gas chromatography-mass spectrometry-computer system. The minimum detectable amount of benthiocarb in water sample by gas chromatography was 0.56 ng and about 100 ng of benthiocarb could be identified by a gas chromatography-mass spectrometry-computer system.     

Electron-microscopic imaging of single-walled carbon nanotubes grown on silicon and silicon oxide substrates

Direct imaging of single-walled carbon nanotubes (SWNTs) suspended on pillar-patterned Si or SiO2 substrates is investigated using transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The suspended nanotubes are successfully observed by direct TEM imaging and it is seen that they have either individual or bundles of SWNTs. Low energy (< or =2 keV) SEM produces high contrast images of suspended SWNTs. On the contrary, when SWNTs contact a SiO2 substrate, they are imaged using electron-beam induced current. The image brightness depends on the length of SWNTs.     

Development of a micro total analysis system incorporating chemiluminescence detection and application to detection of cancer markers

We developed a micro total analysis system (mu-TAS) incorporating chemiluminescence detection, in which the chemiluminescence reaction of isoluminol isothiocyanato (ILITC) (as a chemiluminescence reagent for labeling)-microperoxidase (as a catalyst)-hydrogen peroxide (as an oxidant) was adopted. The analysis system performed the following three processes on a microchip: immune reaction for high selectivity, electrophoresis for formation and transportation of the sample plug, and chemiluminescence detection for high sensitivity. The three processes were compactly integrated onto the microchip to give the mu-TAS. The microchip contained two microchannels that crossed at an intersection, while the ends of the microchannels accessed four reservoirs. As the first process, the immune reaction was performed using an antibody-immobilized glass bead. The glass bead was placed in one of the reservoirs along with antigen (analyte) and a known amount of ILITC-labeled antigen to set up a competitive immune reaction. For electrophoresis, as the second process, the reactant after the immune reaction was fed electrophoretically into the intersection resulting in a sample plug. The sample plug was then moved into another reservoir containing hydrogen peroxide solution. At this point, chemiluminescence detection was performed as the third process: the labeled antigen mixed with the hydrogen peroxide and the catalyst included in the migration buffer to produce chemiluminescence. Chemiluminescence was detected by a photomultiplier tube located under the reservoir. The mu-TAS described here was capable of determining, with high selectivity and sensitivity, human serum albumin or immunosuppressive acidic protein as a cancer marker in human serum.     

Kinetic study of thermostable L-threonine dehydrogenase from an archaeon Pyrococcus horikoshii

In the genome data base of the hyperthermophilic archaeon Pyrococcus horikoshii, an open reading frame with sequence homology to a gene encoding alcohol dehydrogenase was found. It was demonstrated that the encoded enzyme was a thermostable L-threonine dehydrogenase which can oxidize the hydroxy alkyl residue of L-threonine associated with the reduction of NAD+ or NADP+. This enzyme is a member of the zinc-containing L-threonine dehydrogenase family. One enzyme molecule contained one zinc atom, and this metal was considered to contribute to the hyperthermostablility of the enzyme. The reaction of the enzyme proceeded via a sequential mechanism. The Michaelis constants (Km) for L-threonine and NAD+ were 0.013 and 0.010 mM, respectively, and the maximum reaction rate (Vmax) was 1.75 mmol NADH formed/min/mg-protein at 65 degrees C. The Km values for both L-threonine and NADP+ were larger than those for L-threonine and NAD+ with a similar Vmax value. These results indicate that the enzyme has lower affinity to NADP+ than to NAD+, and the binding affinity for L-threonine depends on the coenzymes.