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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Stereoselective synthesis of , - and , Z-β-ionylideneacetaldehydes was accomplished from the β-ionone tricarbonyl iron complex, and the latter was converted to Z-retinoic acid.

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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 DESRA2 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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Activity-directed isolation of the ethyl acetate, methylene chloride and n-hexane fractions of Gloiopeltis furcata resulted in the isolation of 18 compounds. Their structures were elucidated as 2-(3-hydroxy--oxotetrahydrofuran-3-yl)acetic acid (1), glutaric acid (2), succinic acid (3), nicotinic acid (4), ()-4-hydroxyhex-2-enoic acid (), cholesterol (6), -hydroxycholesterol (), uridine (), glycerol (), -(hydroxymethyl)-2-methoxybenzene-1,3-diol (10), (,)--oxodeca-,-dienoic acid (11), (Z)-3-ethylidene-4-methylpyrrolidine-2,-dione (12), dehydrovomifoliol (13), loliolide (14), cholesteryl stearate (15), palmitic acid (16), cis-,,11,14,17-eicosapentaenoic acid (17) and α-linolenic acid (18) on the basis of spectroscopic and chemical evidences. Their anticholinesterase and antioxidant activities were evaluated via inhibitory activities on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) as well as scavenging activities on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical and peroxynitrite (ONOO⁻). All isolated compounds (1—18) exhibited moderate AChE inhibitory activities with IC₅₀ values ranging from 1.14—12.50 μg/ml, whereas 1, , , 17, and 18 showed mild BChE inhibitory activities with IC₅₀ values ranging from .57—15.89 μg/ml. Although most of the compounds isolated were lacking the scavenging activity on DPPH radical and ONOO⁻, and 10 showed good DPPH radical scavenging activity, and , 10, and 16 showed potent ONOO⁻ scavenging activity.

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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 (700–1,500 μm tall). On 2% 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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A long term follow-up of patients after antero-lateral partial vertebrectomies (ALPV) was performed using patient charts and questionnaires. During the past 15 years, ALPV has been performed on 159 patients with cervical spinal disorders. Among them, 136 patients whose survey was performed more than 1 year ago were selected. were male and 44 were female. Their ages ranged from 41 to 82, and the average age was 63.1. The follow-up period was from 1 to 14 years (the average being 3. years). Pathology included spondylosis 119, OPLL 31, canal stenosis and combined lesion cases. Surgical resuts were evaluated using a grade scale (excellent ; , good ; G, fair ; , poor ; P and dead ; D). At discharge, group was 40.2%, G was 51.%, was .2%, P was 0%, D was 0.%. At the end of the follow-up period was 36.%, G was 35.%, was 20.2%, P was .1% and dead was .%. None of the deaths were related to the surgery. However, the score obtained from the Neurosurgical Cervical Spinal Scale were essentially consistent. Results of the questionnaire showed that 61.4% of the patients were satisfied, 30.1% were fairly satisfied and only .4% were dissatisfied. Dissatisfied cases included 2 cases of surgical failure but most of them were related to the progressive worsening of other lesions such as thoracic, lumbar spinal lesions or peripheral neuropathy. In 2 cases reoperation was performed, one anterior fusion with fibular strut graft for kyphoscoliosis and the other anterior fusion with a mini-plate for a fracture of the lamina and slippage of the vertebral body. In some cases, weakness of the root area was encountered but most of these were resolved in a few months. Radiologically, the bony defects of the vertebral body were observed to become smaller, namely they were replaced by new growth of bone slowly in all cases. Thus, ALPV seems to be a useful surgical procedure for multilevel cervical spinal disorders.

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From the fronds of Polystichum tripteron (KUNZE) P_R. a new norcarotenoid glycoside was isolated and shown to be (6R, , R)--hydroxy-megastigma-4, -dien-3-one--O-β-D-glucoside. The fronds of Dennstaedtia wilfordii (MOORE) CHRIST. contain the same glucoside.

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Eight new sterols, , -epidioxy-(, 24R)-23-methylergosta-6, -dien-3β-ol (1), 3β, , -trihydroxy-(, 24R)-23-methylergosta-, -dien-6-one (2), 3β, , -trihydroxy-(24S)-ergost--en-6-one (3), 3β, , , 14α-tetrahydroxy-(, 24R)-ergosta-, -dien-6-one (4), (, 24R)-ergosta-, -diene-3β, , 6α, -tetrol (), , -epidioxy-3β-hydroxy-(, 24R)-ergosta-, -dien-6-one (6), , -epidioxy-3β-hydroxy-(24S)-ergost--en-6-one () and , 6α-epoxy-(, 24R)-ergosta-, -diene-3β, , 14α-triol (), have been isolated from five edible mushrooms, Lentinus edodes, Flammulina velutipes, Hypsizigus marmoreus, Pleurotus ostreatus and Pholiota nameko together with fifteen known ones (-23), of which two (16 and 17) are reported for the first time from a fungal source. The structures of these new compounds were elucidated on the basis of their spectral data.

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Four new sterols, , 6α-epoxy-(, 24R)-ergosta-(14), -diene-3β, -diol (1), (, 24R)-ergosta-, -diene-3β, , 6β, -tetrol (2), (, 24R)-ergosta-, (11), -triene-3β, , 6β-triol (3) and 3β, , 6β-trihydroxy-(, 24R)-ergost--en--one (4), have been isolated from the fruit bodies of Grifola frondosa (FR.) S. . GRAY (Polyporaceae)together with fourteen known ones (-18), of which two ( and 6) are reported for the first time from a natural source. The structures of these compounds were elucidated on the basis of spectral data.

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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 -3dB frequency bandwidth, group delay ripple, 3rd-order distortion, and 3rd-order input intercept point (IIP3) were 200MHz, 2.2%, ≤ -55dB with a 100MHz input, and +10.3dBm, respectively, all with a ±0.1Vp-p input signal at each input terminal in the pseudodifferential configuration. The LPF including an output buffer dissipated 60mW in the case of a 1.2V supply. Wide spurious-free dynamic range (SFDR) characteristics were confirmed up to high frequencies.

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Six new cembranoids sarcophytol P (3), R (4), S (), K (), (11), and T (13) were isolated from the soft coral Sarcophyton glaucum. Sarcophytol P (3) was shown to be the 20-hydroxy derivative of the major component sarcophytol A (1), and afforded the cyclization product 6 in CHCl_3 at room temperature, in a same way as in 1. Sarcophytols R (4) and S () were correlated to 1, by conversion of its R,R and S,S epoxide derivatives. Sarcophytol K() was a 13, 14-dihydroxycembranoid having a 1,3Z-diene moiety. The absolute configuration of and its 1Z,3- and 1Z,3Z-isomers sarcophytol B (2) and J (10) were determined by circular dichroism study of their bis-p-dimethylaminobenzoate derivatives. Sarcophytols (11) and T (13) were 1- and 1,3Z-isomers of 1. Compound 11 showed characteristic broadening of the ^1H-NMR chemical shifts, due to the restricted conformational interconversion. Using the three cembranoids sarcophytols (11, 1,3), N (15, 1Z,3Z) and T (13,1,3Z), spontaneous autoxidation-cyclization, in CHCl_3,was examined, in order to compare the stereochemical course of the reaction with that of 1 (1Z,3), which affords trans-fused bicyclo[.3.0]tetradecene systems. The 1,3Z-isomer 13 gave the same cyclization product 18, as in the reaction of 1, even though it is isomeric at -1,3. The 1Z,3Z isomer 15 gave 19, in consequence of the reversed geometry at -3 of 15. The 1,3-isomer (11) gave the bicyclic product , having an antipodal fusion as compared with 19. This was confirmed by PCC oxidation of 19 and , giving enantiomeric ketones 23 and 24 respectively. The 1(14)-epoxide 26 was shown to be the immediate precursor of , and acounted for the inversion of the geometry at -1 of the cyclization product. Compound 26 is isomeric with the epoxide 17 derived from 1. The epoxide 17 is the postulated precursor in the conversion of 13 to 18. It is noteworthy that the mode of antipodal fusion of the cyclopentane rings, in 18 and , was controlled by the chirality of the epoxy rings. The -14 hydroxyl group participates in the transannular cyclization, but was found not to be the requisite functional group for the reaction. Similar treatment of cembrene (30), the parent hydrocarbon of 1, also reacted in CHCl_3 giving the bicyclic product 32.

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Two new partially saturated tricyclic ring systems, 6, 6a, , , , 10, 10a, 11-octahydro-11-oxodibenz [b, ] oxepins (3a and 3b), and -thiepins (4a and 4b) were synthesized. Compounds 4a and 4b were desulfurized to give a pair of isomeric 2-methylbenzoylcyclohexanes (10a and 10b). Deuterated 4a and 4b (11a and 11b) were prepared starting from butadiene-d₆ (12). The stereochemical features of 3a (trans), 3b (cis), 4a (trans) and 4b (cis) are compared with those of 10a, 10b, 11a and 11b on the basis of proton nuclear magnetic resonance data.

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Six new sterols, , 6α;, -diepoxy-(, 24R)-ergost--ene-3β, -diol (1), , 6α;, -diepoxy-(, 24R)-ergost--ene-3β, -diol (2), , 6α-epoxy-(, 24R)-ergosta-, -diene-3β, -diol (3), (, 24R)-23-methylergosta-, -diene-3β, , 6β-triol (4), (, 24R)-23-methulergosta-, -diene-3β, , 6β, -tetrol () and (24S)-ergost--ene-3β, , 6β, -tetrol (6), have been isolated from seven mushrooms, Amanita pantherina, Amantia virgineoides, Lactarius piperatus, Lyophyllum shimeji, Tricholoma portentosum, Hypsizigus marmoreus and Lentinula edodes together with eighteen known ones (-24). The structures of these new compounds were elucidated on the basis of their spectral data.

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 The stability of

‒tetrahydrocannabinol acetate (‒THC‒OAc) and ‒tetrahydrocannabinol acetate (‒THC‒OAc) in -liquid during storage was investigated. ‒THC‒OAc liquids in cartridges were stored at 80℃ or 30℃ for 28 days. The relative concentrations of cannabinoids in the liquids were measured by gas chromatography with flame ionization detection. ‒THC‒OAc decreased during storage at either temperature. ‒THC, a minor impurity, also decreased. ‒THC‒OAc liquid in a cartridge was stored at 80℃ for 57 days. The concentration of ‒THC‒OAc and ‒THC, a minor impurity, did not change during that time. Cannabinol acetate increased in all liquids, and unknown products were also detected by gas chromatography/mass spectrometry (GC/MS). The ‒THC‒OAc and ‒THC‒OAc liquids were subjected to GC/MS to detect representative diluents, glycerol, propylene glycol, and polyethylene glycol 400, but none of these were detected.

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Reactions of nor-diterpenoid dilactones isolated from Podocarpus plants have been investigated. The : ,: 11-dienolide type [] dilactones, the least available but biologically the most active members, are mainly derived from naturally abundant dilactone components of α-pyrone type [A] and : -epoxy-: 11-enolide type [B] for total-synthetic and biological purposes. From nagilactone (), for example, a combined sequence of hydrogenolysis of : -epoxide group and dehydration gives nagilactone (), 3β-hydroxynagilactone () and 2: 3-dehydronagilactone (19), which have been found from natural sources. From nagilactone A (1), photo-hydration and concomitant double bond migration of its acetate results in a lactol (), which is reduced to 1β-hydroxynagilactone (), another natural type [] dilactone. Derivation of the type [A] or [B] from others is not successful. Some attempts for conversion of the ring A functional groups have also been studied.

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