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Calcium salts of long-chain fatty acids from palm fatty acid distillate (CaPFAD) and soybean oil (CaSOFA) were compared using 14 first lactation and 26 multiparous Holstein cows housed in a free-stall barn. It was hypothesized that if replacing CaPFAD with CaSOFA, a rich source of linoleic acid, could result in increased conjugated linoleic acid (CLA) content in milk without losing the lactational and reproductive benefits of feeding CaPFAD, this would be beneficial to the dairy industry and public health, as well as potentially enhance the consumption of dairy products. Cows were group-fed one of two total mixed rations (TMR) containing 1.7% CaPFAD or CaSOFA (DM basis) for ad libitum intake following recommendations from the manufacturer of the fat supplements. Fatty acid profiles (g/100 g of fatty acid) of CaPFAD and CaSOFA, respectively, were 16:0: 48.1, 12.1; 18:0: 4.27, 5.34; 18:1: 35.7, 23.9; and 18:2: 8.9, 51.2. Cows spent about 45 days in the fresh group, after which they were moved to high producing group where they stayed up to 10 weeks post-partum within their treatment assignments. The TMR (DM basis) were 50:50 forage:concentrate for both the fresh group and high producing group cows and contained (DM) 28% NDF and 18% CP. There were no treatment differences in milk yield, milk fat percentage, milk CLA content, milk true protein percentage, milk lactose percentage, milk urea N, linear somatic cell count and change in body condition score. Cows fed CaSOFA produced milk containing a higher content of 18:1(t) (P

CdS/CdTe solar cells have attracted attention recently for their potential as low-cost, high-efficiency solar cells of the future. It is because the CdTe layer (used for photoelectric conversion) has a bandgap energy of 1. 51 eV, which corresponds well to sunlight spectra, and the direct transition type energy band structure enables formation of thinner films. We have already industrialized CdS/CdTe solar cells in mass production stage using a printing-sintering process, as large-area modules for electric power generation(Higuchi et al. , 1993, Omura et al. , 1991), and as cells for indoor applications (primarily in calculators. Suyama et al. , 1986). However, this solar cell has a conversion efficiency of approximately 6%. Recently, there has been considerable research into thin-film CdS/CdTe solar cells which have a thinner CdS film formed by CVD or CBD (Britt et al. , 1993) process, and thus are photosensitive to light with wavelengths of 500 nm or less. At present stage of our art, in solar cells formed by the CSS with a CdTe film on CVD CdS, a conversion efficiency of 15. 05% has been obtained in cells with an area of 1 cm2 (verified at JQA).

Tungsten disulphide crystals used as lubricants have been studied by high resolution transmission electron microscopy (HRTEM). Theoretical calculation of the HRTEM image using the multislice method shows that the WS2 [2 1 1 0] images can distinguish between the W and S columns along the incident electron beam and enable one to determine not only the crystal structure but also the fault structure. Observation of a WS2 [2 1 1 0] crystal, prepared by grinding, discloses stacking faults and an array of edge dislocations whose extra planes are single S-W-S layers, revealing the stacking sequence of W and S layers, and also the stepwise structure of its (0001) surfaces as a result of the shear strain. The lubrication mechanism for solid lubricants such as WS2 and MoS2 is interpreted microscopically in terms of the crystallography on the basis of the observation.

Catecholamines can overcome myocardial stunning. However, a previous report on energy metabolism in stunned myocardium during catecholamine infusion was based on the conventional biochemical methods which might affect contractile function. Twenty farm pigs were anesthetized and underwent 15 min coronary artery occlusion and 2 h reperfusion. Ten pigs were given 10 micrograms/kg/min dobutamine from immediately after and throughout the reperfusion (dobutamine group). The other ten pigs were given saline (control group). Phosphorus-31 magnetic resonance spectroscopy and sonomicrometry were done alternately. Dobutamine improved percent segment shortening after reperfusion (control/dobutamine = 3.8%-5.7%/11.7%-13.4%; P0.01). At 15 min ischemia, adenosine triphosphate (ATP) decreased (control/dobutamine = 72 +/- 8%/73 +/- 10%, n.s.), and remained depressed after reperfusion in both groups. After reperfusion, phosphocreatine (PCr) returned to and maintained the preischemic value in the dobutamine group, while in the control group, PCr overshoot (112 +/- 5%) was observed. Except for the presence and absence of PCr overshoot, there was no significant difference of ATP and PCr between the two groups, although rate pressure product was significantly higher in the dobutamine group than in the control group. Regional myocardial blood flow after reperfusion was significantly higher in the dobutamine group. Dobutamine may improve "stunning" through effective improvement of energy utilization and production, indicated by the disappearance of PCr overshoot and maintained ATP level.

To assess the protective effect of verapamil on ischemic myocardium, the changes in high energy phosphates, inorganic phosphate, and intracellular pH were serially and quantitatively measured in ischemic porcine hearts without collateral circulation using 31 P-NMR spectroscopy, together with ultrastructural examination. Twenty-six farm pigs weighing 11 to 14 kg were anesthetized with fluothane and were divided into control (C) group and verapamil pretreatment (V) group. In V group 0.2 mg/kg of verapamil was administered for 20 mins before occlusion of the anterior descending cornary artery. 31 P-NMR spectra were serially obtained throughout the experiment, and ultrastructural examination was done at 20-min occlusion and at 120-minute occlusion in each group. At 10-min ischemia, creatin phosphate was significantly preserved in V group ( C V = 11 ± 4% 16 ± 5% P ). At 20 min ischemia, ATP was significantly preserved ( C V = 60 ± 9% 73 ± 8% P ), and intracellular pH was significantly higher in V group ( C V = 6.4 ± 0.2 6.6 ± 0.1 P ). Morphologically, clumping of the nuclear chromatin, mitochondrial swelling and decrease in glycogen were milder in V group at 20 min ischemia. However, these beneficial effects disappeared at 120 min ischemia. Thus pretreatment with verapamil attenuated depletion of high energy phosphates, progression of acidosis, and ultrastructural changes. There was no significant difference of rate pressure product and regional blood flow between hearts with and without pretreatment of verapamil. Therefore, this protective effect may be due to the energy sparing effect or other direct subcellular effect of verapamil on ischemic myocyte.