The ability of Climacodon septentrionalis to immobilize and kill a mycophagous nematode (Aphelenchoides sp.) in vitro is described for the first time. Two isolates produced droplets (20–45 μm in diameter) that formed at the apices of tall, stalked, and branching secretory cells (700–

,500 μm tall). On % modified malt extract agar, nematodes became enveloped in the droplets, which restricted their ability to move and resulted in complete immobilization and death within several hours of contact. The rate of decomposition of the nematodes varied considerably, with most individuals persisting for weeks whereas others were degraded within several days and appeared to be colonized by dense hyphal growth. This study provides the first documentation of a non-agaricoid fungus producing secretory cells that are able to immobilize nematodes.

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Two new partially saturated tricyclic ring systems, , a, , , , 10, 10a, 11-octahydro-11-oxodibenz [, ] oxepins (a and ), and -thiepins (a and ) were synthesized. Compounds a and were desulfurized to give a pair of isomeric -methylbenzoylcyclohexanes (10a and 10). Deuterated a and (11a and 11) were prepared starting from butadiene- (12). The stereochemical features of a (trans), (cis), a (trans) and (cis) are compared with those of 10a, 10, 11a and 11 on the basis of proton nuclear magnetic resonance data.

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One method currently being considered for the disposal of high level radio-active waste is burial in the seabed. When a hot object is buried in soil, the temperature of the soil adjacent to the object is raised and there is transient heat flow away from the object. The rise in the temperature of the soil causes excess pore pressures to be generated and transient pore water diffusion also takes place. A finite element formulation of the coupled heat flow and consolidation problem is presented. The computer implementation of this formulation is found to compare favourably with analytical solutions based on the same physical principles.

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11-Amino-, a, , , , 10, 10a, 11-octahydrodibebenzo[, ]thiepines (a-) and -oxepines (a-) were synthesized by the Leuckart reaction of , a, , , , 10, 10a, 11-octahydro-11-oxodibenzo[, ]thiepines (a, )and -oxepines (a, ) followed by hydrolysis of the reaction products a- and a-, respectively. The four diastereomers, cis(a-H, 10a-H)-cis(10a-H, 11-H) a and a, cis(a-H, 10a-H)-trans(10a-H, 11-H) and , trans(a-H, 10a-H)-trans(10a-H, 11a-H) and , and trans(a-H, 10a-H)-cis(10a-H, 11-H) and , were isolated and their configurations and conformations were elucidated by chemical methods together with

1H

-nuclear magnetic resonance spectroscopic and X-ray crystallographic analyses.

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Repetitive liquefactions in angular and subangular gravels from an alluvial fan, in the case of two earthquakes with accelerations lower than that of a former which had caused liquefaction some months before, are described. The liquefaction took place from the surface, down to a depth of approximately 10 m. Water laden with sediments spouted out for some tens of minutes after the strong motion ceased. Knowledge of the grain size distribution of the sediments inside the body of the alluvial fan roughly defines the areas of the fan prone to future liquefaction. Non-repetitive liquefaction in overconsolidated fine fluvio-lacustrine sand of glacial origin at the unusual depth of 14 m to 16 m is also described. From the observation of sand lifted up for 10 m inside a large diameter well, and of that which spouted out from several microvents, it was estimated that extra-pore pressure was close to lithostatic conditions. Nevertheless, modeling of intrinsic pore pressure buildup on the DESRA programme gives lower values than the experimental one. Geotechnical characteristics of the 12 m-thick sandy stratum indicate that the upper part is unusually soft, either due to water circulation or past repetitive liquefactions which prevented reconsolidation. It is suggested that excess pore pressure generated by the earthquake was also due to redistribution of pressure from adjacent sediments.

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A sample of [

3H

] tobrarnycin (

5

, 000 Ci/Mole) has been synthetized and incubated with
the bacterial ribosome and its subunits. The results obtained show that this antibiotic has
two types of binding sites. The primary one is probably responsible for the inhibition of
protein synthesis whereas the secondary one is probably related to the misreading and reading
tiirough of the messenger RNA.

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Circuit techniques to enhance the linearity of input-voltage-to-current (V/I) conversion and to increase the output impedance of a current source by compensating for the low intrinsic gain of a transistor were introduced to realize a high-frequency operational transconductance amplifier (OTA) for a low supply voltage using sub-100-nm CMOS processes. Applying these techniques, a MOS th-order Gm- linear-phase low-pass filter (LPF) was realized using a 65nm CMOS process. A simplified biquad LPF that can serve as a component of a th-order LPF was newly developed by replacing OTAs with resistors. As a result, the -dB frequency bandwidth, group delay ripple, rd-order distortion, and rd-order input intercept point (IIP) were 200MHz, .%, ≤ -55dB with a 100MHz input, and +10.dBm, respectively, all with a ±0.Vp-p input signal at each input terminal in the pseudodifferential configuration. The LPF including an output buffer dissipated 60mW in the case of a .V supply. Wide spurious-free dynamic range (SFDR) characteristics were confirmed up to high frequencies.

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カンキツ主要12種を用いて染色体のクロモマイシン (CMA) 染色を行った．染色体は CMA(+) バンドの有無および位置から 種類に区分できた．すなわち，CMA(+) を A: 両端および動原体近傍に有する，: 一方の端部と動原体近傍に有する，: 両端に有する，: 一方の端部に有する，: CMA(+) がない，: 動原体近傍に有する，Dst: 付随染色体を有する 型，である．各種はこれらのうち ～ 種類の染色体を有し，独自の CMA バンドパターンを示した．

C

. medica では + + ，

C

. limon では + + + ，

C

. aurantifolia では + + ，

C

. aurantium では A + + + + ，

C

. sinensis では + + + ，

C

. maxima では A + + + ，

C

. paradisi では A + + + ，

C

. ichangensis では + + 12 + ，

C

. latipes では A + + + ，

C

. micrantha では + 11 + + Dst，

C

. macroptera では + + 11 + + ，

C

. hystrix では + + + + + Dst であった．

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The activities of tobramycin derivatives acetylated and ethylated on the '-N, '-N and -N positions were examined. The MICs of these derivatives against tobramycin sensitive strains indicated that '-N-ethylated and '-N-ethylated derivatives have a fairly good activity, and confirmed that the -N position is the most important one for antibiotic activity since -N derivatives were less active. The MICs of these derivatives against tobramycin resistant strains, and their inactivation by tobramycin modifying enzymes were examined. These results showed that '-N or '-N ethylation protects the drug against inactivation by AAC(') or AAC('), respectively, and '-N-ethyltobramycin and '-N-ethyltobramycin were active against strains containing these modifying enzymes. On the other hand, -N ethylation protects the drug against inactivation by AAC() but -N-ethyl tobramycin does not inhibit strains containing this enzyme.

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(

3H

) Tobramycin was used as a probe to determine the relationship between the structure of aminoglycoside antibiotics and their ability to remove this drug from its higher affinity binding site on the ribosome. The dissacharide moieties (neamine, tobramine, gentamine) appeared to have a common binding site, whereas the kanosamine, garosamine and ribose moieties determined the specificity of this binding. Amikacin and butikacin behaved in an anomalous manner in spite of their close structural relationship to tobramycin.

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-Benzyl--chloro--mercapto- (H)-pyridazinone () was heated in ethanol under reflux for 10 hours to form concurrently , -dibenzyldipyridazo [, - : ', '-]-, -dithiin-, (H, H)-dione (Ia) (57% in yield) and , -dibenzyldipyridazo [, - : ', '-]-, -dithiin-, (H, H)-dione (IIa) (14% in yield). Assignment of the two products to the corresponding structures is established by their physico-chemical constants and chemical behaviors. The concurrent formation of the dipyridazo [, - : ', '-]-, -dithiin-, (H, H)-dione and the -, (H, H)-dione were observed in, not only heating -chloro--mercapto- (H)-pyridazinones (-) in polar solvent, but warming -mercapto--chloro- (H)-pyridazinones (-) in the presence of potassium carbonate in DMF. For the interpretation of the reaction, keto-thioketo carbenes as active intermediate species and a reversible interconversion among them are suggested on the basis of the fact that there was nonexistence of an equilibrium between the two compounds, such as Ia and IIa, under the reaction condition and a trapping keto-thioketo carbene species as -phenylimino--benzylpyridazo [, -]-, -dithiol- (H)-one (IVa) (14% in yield) along with the major products, (Ia) and (IIa), was furnished by warming with phenylisothiocyanate in the presence of triethylamine in dry benzene. On the contrary, participation of a reversible interconversion between Ia and IIa, to a considerable extent, with the concurrent formation of them in the case of benzylation of either Ib or IIb, by warming with benzylchloride in the presence of potassium carbonate in DMF at 80°, might not be neglected, because an attempted approach to an equilibrium between Ia and IIa in a similar reaction condition except the use of benzylchloride realized, whereas non-existence of an equilibrium between Ib and IIb in the similar reaction condition was observed.

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A biosynthetic pathway for (

)-methyl cinnamate formation was evaluated in Tricholoma matsutake by tracer experiments using

13C

- and

2H

-labeled precursors. One hundred percent selective

13C

incorporation was observed when L-[

1

,

2

,

3

,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

, ^15/N]phenylalanine was converted to (

E

)-[

1

,

2

,

3

,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

]cinnamate and (

E

)-[

1

,

2

,

3

,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

]methyl cinnamate. Similarly, 100% selective

13C

incorporation was observed when (

E

)-[

1

,

2

,

3

,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

]cinnamate was converted to (

E

)-[

1

,

2

,

3

,

4

,

5

,

6

,

7

,

8

,

9

-

13C₉

]methyl cinnamate. In contrast, the

2H

incorporation selectivities were 82.

1

% and

81

.

4

% when L-[

2

,

3

,

4

,

5

,

6

,

7

,

7

,

8

-

2H₈

]phenylalanine was converted to (

E

)-[

2

,

3

,

4

,

5

,

6

,

7

,

8

-

2H₇

]cinnamate and (

E

)-[

2

,

3

,

4

,

5

,

6

,

7

,

8

-

2H₇

]methyl cinnamate, respectively. Thus, T. matsutake synthesizes (

E

)-methyl cinnamate from L-phenylalanine via (

E

)-cinnamate. (

E

)-cinnamate was likely formed through two pathways: one was major and the other was a minor.

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The behavior of the soft clay grounds subjected to repeated loading is different from that subjected to sustained loading. The difference in settlement between these two loading patterns should be due to secondary compression over a long period of time. Consequently, soft clay grounds subjected to repeated loading tend to be more compressible than those subjected to sustained loading. Therefore, it is necessary for engineers to predict post-construction settlements under repeated loading. In this respect, the preloading is considered to be promising as a countermeasure to reduce the settlement of clay under repeated loading as well as under sustained loading. The effect of preloading on post-construction consolidation settlement of soft clay subjected to repeated loading after removal of a part of preload is investigated in the present paper. It has become clear that the settlement of a clay sample after preconsolidation is mainly affected by the amount of preload, the degree of consolidation due to the preload, the amount of permanent load and the amount of repeated load after removal of preload. The calculated settlement versus time relations using a method to estimate the amount of consolidation settlement of soft clay grounds subjected to repeated loading after removal of preloading were compared with the observed degree of consolidation as parameters of the intensities of preload and repeated load.

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わが国における主要中晩生および香酸カンキツ染色体のクロモマイシン (CMA) 染色を行った. 染色体はCMA(+) バンドの有無および位置から種類に区分できた. すなわち, CMA(+) をA: 両端および動原体近傍に有する, : 一方の端部と動原体近傍に有する, : 両端に有する, : 一方の端部に有する, : CMA(+) がない, である. 各種はこれらのうち, 種類の染色体を有し, 独自のCMAバンドパターンを示した. ハッサクではA+++, ヒュウガナツではA+++, ‘川野なつだいだい’ではA+++, ‘宮内伊予柑’ではA++++, タンカン‘垂水号’ではA++++, カボスでは+++, スダチでは+++およびユズ‘山根’では++11+であった. 以上の結果, 本研究においても近縁の種間では似通ったCMAバンドパターンが観察された.

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