Acceleration and filtering in the generalized Landweber iteration using a variable shaping matrix

The generalized Landweber iteration with a variable shaping matrix is used to solve the large linear system of equations arising in the image reconstruction problem of emission tomography. The method is based on the property that once a spatial frequency image component is almost recovered within in in the generalized Landweber iteration, this component will still stay within in during subsequent iterations with a different shaping matrix, as long as this shaping matrix satisfies the convergence criterion for the component. Two different shaping matrices are used: the first recovers low-frequency image components; and the second may be used either to accelerate the reconstruction of high-frequency image components, or to attenuate these components to filter the image. The variable shaping matrix gives results similar to truncated inverse filtering, but requires much less computation and memory, since it does not rely on the singular value decomposition.     

Resonance Raman and optical transient studies on the light-induced proton pump of bacteriorhodopsin reveal parallel photocycles

The photocycle of bacteriorhodopsin (bR) was studied at ambient temperature in aqueous suspensions of purple membranes using time-resolved resonance Raman (RR) and optical transient spectroscopy (OTS). The samples were photolyzed, and the fractional concentrations of the retinylidene chromophore in its parent state, BR570, and in the intermediate states L550, M412, N560, and O640 were determined in the time domain 20 microseconds-1 s and in the pH range 4-10.5. Two kinetically different L components could be identified. At pH 7 one fraction of L (approximately 65%) decays in 80 microseconds to M (deprotonation of the Schiff base), whereas the residual part is converted in approximately 0.5 ms to N. The RR spectra reveal only minor structural changes of the chromophore in the L-->N transition. These were attributed to a conformational change of the protein backbone [Ormos, P., Chu, K., & Mourant, J. (1992) Biochemistry 31, 6933]. With decreasing pH the L-->N transition is delayed to > 2 ms following a titration-like function with pKa approximately 6.2. The decay of M412 monitored by OTS can be fitted for each pH value by two different amplitudes and time constants (Mf, tau f; Ms, tau s; f = fast, s = slow). Both Mf and Ms consist of subcomponents which can be distinguished by their different reaction pathways (but not by OTS). Mf occurs in the reaction sequences L-->Mf-->N-->BR and L-->Mf-->O-->BR. The population of the first sequence, in which N is formed with the time constant tau f (approximately 2-4 ms, pH 6-10.5), increases with pH. Ms is also found in two different reaction sequences of the form L-->Ms-->BR. The quantitative analysis reveals that each "titration effect" can be related to a certain fraction of bR. It is proposed that each fraction can be identified with a "subspecies" of bR which undergoes an independent and individual cyclic reaction. A complete reaction scheme is set up which represents the manifold of observed phenomena. It is concluded from the pH dependence of the lifetimes of Ms and N that the reconstitution of BR570 in the reaction steps Ms-->BR and N-->BR requires the uptake of a proton from the external phase. It is argued that this proton catalyzes the reisomerization of retinal, whereas the Schiff base is internally reprotonated from Asp-85. A model for proton pumping is proposed in which the proton taken up from the external phase to catalyze the reisomerization of retinal is the one which is pumped through the membrane during the photocycle of bR.     

Fluid dynamics of a quantized vortex filament in a hole

The behavior of nucleated vortex loops and of remanent vortex filaments in idealized circular and slit-like orifices has been investigated by direct computation. It is found that such vortices can be stretched by the diverging flow on the exit side of the orifice. The energy needed to stretch the vortex is abstracted from the flow field and observed as dissipation. This occurs in the form of discrete phase-slip events in the case of nucleated vortex loops, and in the form of multiple-phase-slip cascades when a remanent vortex is involved.     

Photolithography of amorphous films of (η5-C5H5)2Ti(N3)2 on silicon (111) resulting in TiO2: The mechanism of the photodeposition reaction

Photolithography to produce TiO₂ patterns from amorphous films of (⁵-C₅H₅)₂Ti(N₃)₂ has been demonstrated. The efficiency of the reaction has been measured yielding a quantum yield of 0.025. The mechanism of the photoreactions of (⁵-C₅H₅)₂Ti(N₃)₂ has been studied using Fourier transform-infrared spectroscopy in both a low-temperature 1,2-epoxyethylbenzene glass and as surface films. In each case the primary photochemical process was found to be loss of a single azido group. The result of subsequent photolysis was found to be dependent upon medium and temperature. In the low-temperature glass no further photochemistry was observed. The exhaustive photolysis of films at 20 K, or room temperature, under a vacuum or in air led to loss of all ligands and the formation of TiO₂.     

Dielectric properties of apples in the range 0.1–100 kHz

Capacitance and conductance spectra are measured between 100 Hz and 100 kHz for three varieties of apple. Analysis of the spectra for several types of electrode material indicates that electrode effects may be neglected for frequencies above 1 kHz. Power-law responses are observed withCf ^–0.3 for the capacitance andG _a.c.f ^+0.9 for the a.c. conductance. Activation energies were found to be of the order of 0.05–0.15 eV for the three apple varieties and found to be frequency dependent. Comparison is made with an apple in which the cellular structure has been damaged by freezing. Freezing produced a significant increase in the high-frequency activation energy for conductance and a decrease in the power-law exponent to +0.3 for a.c. conductance. It is suggested that the dielectric properties result from a combination of relatively free ionic diffusion in the extracellular medium and the hopping of counterions along trap sites on the cell wall.     

Hydration of tricalcium germanate

The hydration characteristics of tricalcium germanate were examined. Kinetics of tricalcium germanate hydration, and hydration product morphologies and compositions were determined at 5 °C intervals between 5 and 70 °C. Complete hydration was rapidly achieved, X-ray diffraction indicated that tricalcium germanate reacted completely within 2 h at all the temperatures investigated. However, a constant value for an Arrhenius activation energy could not be determined. At hydration temperatures above 45 °C a small heat peak, which preceded the main calorimetric peak, appeared in the calorimetric curves. Calcium hydroxide was rarely observed by SEM for hydration at temperatures below 45 °C. Dense regions of calcium hydroxide were readily observed for hydration above this temperature. In contrast to the hydration of tricalcium silicate, an induction period was not observed nor was an extended period of diffusionally controlled reaction. Calcium germanate hydrate was fibrous with the fibre thickness exhibiting a temperature dependence. Hydration product compositions were determined by thermal gravimetry. Expressing the composition of calcium germanate hydrate as (CaO)_3–x GeO₂·nH₂O, the value of 3–x decreases from 1.68 to 1.59 with increasing temperature from 5–70 °C. The values obtained forn varied inconsistently between 2.4 and 3.3. The unit cell of the calcium germanate hydrate was determined to be monoclinic. Cell parameters werea=1.851,b=1.147,c=0.531 nm and =98.10 °.     

What hospitals expect today from clinical systems

Technology will always be a factor in hospital information system buys. But customers are increasingly looking for vendors that create a sincere, responsive sales relationship. In the end, the quality of support and understanding users receive can make or break a sale.     

Semiempirical and ab initio conformational analysis of 2-methylene-8,8-dimethyl-1,4,6,10-tetraoxaspiro[4.5] decane with application of GIAO-SCF methods to NMR spectrum interpretation

The GIAO-SCF method for calculating isotropic nuclear magnetic shielding values has been utilized to explain certain features in the ¹H-NMR spectrum of 2-methylene-8,8-dimethyl-1,4,6,10-tetraoxaspiro[4.5] decane. Population distributions of the low-energy conformers based on their ab initio energies were used to produce weighting factors for the individual calculated shielding values to calculate the weighted average of the shielding values for a complete set of conformers. The differences in ¹H chemical shifts between the hydrogens of the two methyl groups and between the axial and equatorial hydrogens in 2-methylene-8,8-dimethyl-1,4,6,10-tetraoxaspiro[4.5] decane were shown to be due to energy differences between the chair and boat orientations of the six-membered ring and contribution from a twist-boat conformation. Results suggest a hypothesis that intramolecular differences in chemical shift might be calculated to a greater degree of accuracy than chemical shifts calculated relative to a standard.     

Organized knowledge sharing with book-centered Web sites: An architecture, implementation and analysis

For educators, the World Wide Web offers a valuable technology for knowledge sharing. It can complement more traditional approaches to knowledge sharing such as books and lectures. Here, we identify and differentiate three major approaches for Web-based knowledge sharing: course-centered sites, subject-centered sites, and book-centered sites. A rationale for book-centered sites, those developed to facilitate students’ and instructors’ efforts in courses that use the book, is advanced. We introduce an architecture of features that can guide developers of such sites. This is illustrated by a book-centered site implemented according to the architecture. Several sites for introductory business computing books are compared and contrasted in terms of the architecture, suggesting ways in which each can be extended. This revised version was published online in July 2006 with corrections to the Cover Date.