Autostereoscopic three-dimensional display based on a micromirror array

A novel approach for three-dimensional (3-D) display systems implemented with a micromirror array was proposed, designed, realized, and tested. The major advantages of this approach include the following: (1) micromirrors are reflective and hence achromatic (panchromatic), (2) a wide variety of displays can be used as image sources, and (3) time multiplexing can be introduced on top of space multiplexing to optimize the viewing zone arrangements. A two-view (left and right) 3-D autostereoscopic display system was first constructed. Left- and right-eye views in the forms of both still and motion 3-D scenes were displayed, and viewers were able to fuse the stereo information. A multiview (two left and two right) 3-D autostereoscopic display system was then simulated.     

Sellmeier's equation and the expression of the thermal refractive-index coefficient for a Nd0.007Gd0.993VO4 crystal

The principal refractive indices of a Nd0.007Gd0.993VO4 crystal for wavelengths of 0.488, 0.6328, 1.064, 1.0795, and 1.3414 microm under the temperature range of 20-170 degrees C are measured by the autocollimation method, and the Sellmeier's equation and the expression of the thermal refractive-index coefficient are then obtained. The reliability of these results is checked by comparing the calculated values with the measured values for the measured wavelengths and the temperature region, as well as with the published values by Studenikin et al. [Quantum Electron. 25, 1162-1165 (1995)] for wavelengths of 0.491, 0.546, 0.578, 0.632, 0.808, and 1.062 microm at 20 degrees C. In addition, the birefringence and the thermal coefficient of the birefringence were obtained by measured results. The results show that the birefringence is larger than that of a YVO4 crystal and that the thermal coefficient of birefringence is less than that of a YVO4 crystal. Therefore it can be expected that the GdVO4 crystal is not only an excellent laser crystal but also an excellent birefringent crystal used in a modern optical transmission system as a passive fiber-optic component.     

Excretion of lipids by the liver fluke (Fasciola Hepatica L)

Adult liver flukes kept in a glucoseenriched medium were found to excrete lipids. Analysis of the incubation medium showed that both neutral lipids (including cholesterol and its esters) and polar lipids were released. The rate of lipid excretion was greatly reduced when the excretory pores and mouths of the flukes were ligated. Histochemical examination of the flukes indicated that such lipids, released through the excretory pores, originate in the cells lining the excretory ducts.     

Effects of dietary amino acid balance on the response of dairy cows to an increase of milking frequency from twice to three times daily

An experiment was conducted to examine how the response of dairy cows to a change from twice to three times-daily milking is affected by deficiencies in the dietary supplies of three amino acids, His, Met, and Lys. Six cows were used in a 6 x 6 Latin square with 14-d periods. The three dietary treatments were: grass silage and a cereal-based supplement containing feather meal as the sole protein supplement; the same silage-cereal diet supplying similar amounts of metabolizable and rumen-undegradable protein but with additional amounts of His, Met, and Lys in the form of fish meal; and the fish meal diet with additional metabolizable energy in the form of an additional 2 kg/d of sugar beet pulp. Within each of these dietary treatments, the cows were milked twice and three times daily, making a total of six treatments. When cows were given the feather meal diet, even though dietary metabolizable energy was in considerable excess, a deficiency of specific amino acids prevented any increase in milk yield in response to increasing the frequency of milking from twice to three times daily. In contrast, when cows consumed a similar level of excess metabolizable energy and a similar level of rumen-undegradable protein for which the protein was of better amino acid balance (fish meal), the increased frequency of milking led to increased yield of milk and milk protein.     

Influence of aeration on hydrophobic organic contaminant distribution and diffusive flux in estuarine sediments

Dredging operations, resuspension events during storms, and bioturbation alter the oxic state of estuarine sediments and induce changes in the composition of dissolved and particle-associated natural organic matter. These changes may alter the distribution of hydrophobic organic chemicals (HOCs) in sediments and their diffusive flux across the sediment-water interface. In this study, the impact of aerating anoxic sediments on the distribution and diffusive flux of a model HOC, 2,2',4,4'-tetrachlorobiphenyl (TeCB), was investigated. Anoxic estuarine sediments collected from three sites along a salinity gradient were used to determine site-specific apparent sorption coefficients for porewater dissolved organic carbon (Kpwdoc) and sediment organic carbon (Koc) under anoxic and oxic conditions. A two-compartment sediment flux model was employed to examine the diffusive flux of TeCB under both oxic states. Aeration of anoxic porewaters resulted in significant decreases in porewater dissolved organic matter (DOMpw) aromaticity as indicated by declines in molar absorptivity at 254 nm (p < 0.005). Aeration also resulted in a 9-13% decrease in DOMpw concentration (p < 0.005) at the two sites exhibiting lower ionic strengths; the high ionic strength site did not exhibit a significant change in DOMpw concentration (p > 0.10). The impact of aeration on TeCB distribution and diffusive flux appeared to be site-specific. Aeration of anoxic sediments induced a significant 1.4 log unit reduction in Kpwdoc at the lowest ionic strength site (p < 0.0005), while sediments from the intermediate ionic strength site exhibited a significant 0.6 log unit increase (p < 0.005). No significant change in sorption to DOMpw was observed for the high ionic strength site (p > 0.10). The sediment displaying the drop in Kpwdoc also exhibited a significant 0.4 log unit drop in Koc (p < 0.01), while the other two sites did not exhibit significant aeration-induced changes in sorption to particle-associated organic matter (p > 0.10). No significant change in diffusive flux was observed for two sites (p > 0.10), while a significant 89-110 mg m(-2) yr(-1) increase in diffusive flux was observed at the low ionic strength site (p < 0.10). This latter result represented approximately a doubling in diffusive flux. In the systems studied, facilitation of TeCB transport across the sediment-water interface by organic colloids did not appear important.     

Transformation of the plant growth regulator daminozide (Alar) and structurally related compounds with CuII ions: oxidation versus hydrolysis

As part of a study of metal ion effects on chemical transformations of nitrogen-containing agrochemicals, conversion of daminozide to succinate via cleavage of the hydrazide C-N bond was examined in the presence and absence of divalent metal ions. No conversion was observed in metal ion-free solutions or in the presence of 1.0 mM NiII, ZnII, and PbII. CuII, in contrast, markedly increased rates of daminozide to succinate conversion. Halide ions (CI-, Br-) had no effect on daminozide conversion in the absence of metal ions but markedly increased conversion rates observed in the presence of CuII. The nitrogen-donor ligands ethylenediamine, N-(2-hydroxyethyl)ethylenediamine, and 1,4,7,10-tetraazacyclododecane decreased rates of CuII-facilitated conversion, while 1,5,9-triazacyclododecane actually increased rates of conversion. H NMR and UV spectroscopy provide evidence for the formation of 1:1 CuII-daminozide complexes. Halide ion effects and nitrogen-donor ligand effects point to an oxidative mechanism for CuII-facilitated daminozide breakdown, rather than hydrolysis. The structurally related compound butyric acid 2,2-dimethylhydrazide (BH) is subject to the same CuII-facilitated breakdown via an oxidative mechanism. N,N-Dimethylsuccinamic acid (SA), in contrast, breaks down via a hydrolytic mechanism.     

Soil wettability as determined from using low-field nuclear magnetic resonance

The molarity of ethanol droplet and water drop penetration time methods are commonly used to determine soil wettability because these tests are quick and easy to perform. However, these tests do not provide reproducible results on the same sample. Low-field nuclear magnetic resonance (NMR) is shown as an alternative tool to determine soil wettability. Addition of small amounts of water in dry wettable porous media produces predominant amplitude peaks at transverse relaxation times (T2) of 100 ms or less while addition of water in dry water-repellent porous media with the same pore structure produce predominant amplitude peaks at T2 values near 1000 ms. The geometric mean of T2 (T(2gm)) from water-repellent samples immediately after the addition of water is greater than 1000 ms, which is close to that of bulk water, while T(2gm) from wettable samples immediately after the addition of water is significantly less than 1000 ms. Measurements over time show that water-repellent samples eventually reach the same equilibrium end point as its corresponding wettable sample when continually exposed to water. This paper will show that NMR can be used to formulate a screening criterion for quickly determining wettability. The advantage of using NMR is that the results are reproducible provided the sample is prepared and analyzed in a systematic manner.     

Immobilized particle arrays: coalescence of planar- and suspension-array technologies

Combining positive attributes of planar arrays and suspension arrays, immobilized particle arrays offer a new format in which immobilized submicrometer particles are arrayed on hydrogel-coated slides, providing 100+ assay replicates within each spot. This research describes how to prepare immobilized protein arrays and how to assay the binding of labeled target molecules to the arrayed capture probes. The assay system exhibits an intrinsic dynamic range of two to three decades, with coefficients of variation from 5 to 10%. For antibody-antigen binding, target capture appears to be reaction rate limited. For labeled antibody binding to antigen on the immobilized particles, the detection limit is approximately 0.5 ng/mL. When antibodies on the immobilized particles exhibit multivalent binding of target molecules, the detection limit is approximately 0.01 ng/mL. For protein arrays, potential advantages of this format are improved coating of the capture reagent, an increased number of options for protein presentation, reduced mass transport effects, and higher density multiplexing.     

Interfaces to connect thin-layer chromatography with electrospray ionization mass spectrometry

This study has developed two interfaces to connect small-size thin-layer chromatography (TLC) with electrospray ionization mass spectrometry (ES-MS) for the continuous analysis of organic mixtures. The interfaces are (1) two bound optical fibers inserted into the C18-bonded particles at the exit of a small TLC channel and (2) a small commercial TLC strip with a sharpened tip. A reservoir continuously supplied a makeup solution to the tip of the TLC channel. The high voltage required for electrospray ionization was introduced into the makeup solution or mobile phase through a Pt wire, and electrospray was generated at the tip of the bonded optical fibers and at the sharp end of the TLC strip. Since small-size TLC channels were used, the elution time was short and less than 0.2 microL of the sample solution and 200 microL of the eluting solvent were required. Organic mixtures were separated successfully and detected on-line using the TLC/ES-MS techniques.     

Catalytic wet air oxidation of phenol by CeO2 catalyst--effect of reaction conditions

The effect of catalyst loading, oxygen pressure, reaction temperature and phenol concentration on phenol conversion and total organic carbon (TOC) conversion, using CeO(2) as the catalyst, was investigated. There appeared a maximum rate of phenol conversion and TOC conversion as the catalyst loading increased. With phenol concentrations in the range of 400-2500 mg/L and oxygen pressure of 0.5 or 1.0 MPa, the optimal catalyst loading was 1.0 g/L, while it was 2.0 g/L at an oxygen pressure of 1.5 MPa. With a phenol concentration of 5000 mg/L, the optimal loading was 2.0 g/L for all oxygen pressures tested. Catalyst loading influences the reaction via the free-radical chain reaction involved in the catalytic wet air oxidation of phenol. Regarding oxygen pressures, at a phenol concentration of 400mg/L, the influence of the tested pressures (0.5, 1.0 and 1.5 MPa) on the 3h conversion of phenol was negligible, while the effect was significant for higher concentrations of phenol. The effect of oxygen pressure on TOC conversion was more profound, especially at a higher phenol concentration. At a pressure of 0.5 MPa, except for concentration of 400mg/L, the CO(2) selectivity barely exceed 80% at best, and was less than 25% with a phenol concentration of 5000 mg/L. At a pressure of 1.5 MPa, the selectivity was as high as 90% even for a concentration of 5000 mg/L. As was expected, increase of reaction temperature shortened the time taken to reach 50% phenol conversion. In addition, TOC conversion also increased with reaction temperature. Working from these observed results, optimal operating conditions were proposed.