Open and covered singing as studied by means of fiberoptics, inverse filtering, and spectral analysis

Covering the voice near the passaggio is a technique mainly used in male classic Western singing. The purpose is said to be to smooth the register transition and avoid register breaks. The physiological and acoustical differences between open and covered singing near the so-called passaggio were investigated by means of fiberoptics, inverse filtering, and spectral analysis. The study corroborated previous findings that covering physiologically means a widening and lengthening of the pharynx. Acoustically, covering implies a change of formant frequencies, and an elevated sound pressure level of the lowest source spectrum partial, i.e., the fundamental, resulting from an increased transglottal air flow. The findings indicate that covered singing also is associated with larynx lowering. Covered singing near the passaggio shows similarities to so-called phonation, and is probably preferable from the point of view of vocal hygiene.     

Glottal closure, transglottal airflow, and voice quality in healthy middle-aged women

Seventeen healthy women, 45 to 61 years old, were examined using videofiberstroboscopy during phonation at three loudness levels. Two phoniatricians evaluated glottal closure using category and ratio scales. Transglottal airflow was studied by inverse filtering of the oral airflow signal recorded in a flow mask (Glottal Enterprises System) during the spoken phrase /ba:pa:pa:pa:p/ at three loudness levels. Subglottal pressure was estimated from the intraoral pressure during p occlusion. Running speech and the repeated /pa:/ syllables were perceptually evaluated by three speech pathologists regarding breathiness, hypo-, and hyperfunction, using continuous scales. Incomplete glottal closure was found in 35 of 46 phonations (76%). The degree of glottal closure increased significantly with raised loudness. Half of the women closed the glottis completely during loud phonation. Posterior glottal chink (PGC) was the most common gap configuration and was found in 28 of 46 phonations (61%). One third of the PGCs were in the cartilaginous glottis (PGCc) only. Two thirds extended into the membranous portion (PGCm); most of these occurred during soft phonation. Peak flow, peak-to-peak (AC) flow, and the maximum rate of change for the flow in the closing phase increased significantly with raised loudness. Minimum flow decreased significantly from normal to loud voice. Breathiness decreased with increased loudness. The results suggest that the incomplete closure patterns PGCc and PGCm during soft phonation ought primarily to be regarded as normal for Swedish women in this age group.     

Monolithic beds of artificial gel antibodies

The introductions of the continuous beds, now often called monoliths [S. Hjertén, J.-L. Liao, R. Zhang, J. Chromatogr. 473 (1989), 273-275] and the artificial, highly selective gel antibodies against antigens as large as proteins, viruses and cells [J.-L. Liao, Y. Wang, S. Hjertén, Chromatographia 42 (1996), 259-262] were breakthroughs in the design of chromatographic beds. This paper deals with a combination of these two methods, i.e., the artificial gel antibodies have been synthesized in the monolithic mode. As antigen we have used human hemoglobin. A comparison of the ion-exchange chromatograms of the eluates from the monolithic columns shows that the monolith prepared in the presence of hemoglobin adsorbed this protein, but not the other proteins in the sample (ribonuclease A and cytochrome c), i.e., this monolith was selective for hemoglobin, whereas the blank column (prepared in the absence of hemoglobin) had no selective properties, since none of the applied proteins were adsorbed. The diameter of the column was 6mm, but the same approach to synthesize a monolithic selective bed can very likely also be used for capillaries and microchips.     

Effect of the thorium oxide content on the leaching of a mixed thorium-uranium oxide fuel

Journal of Radioanalytical and Nuclear Chemistry - Leaching of uranium from uranium oxide fuel in contact with water can be a radiation hazard problem in the case of fuel cladding failure, either...     

A one-to-two-dimensional mapping using a partial Fast Fourier Transform

It will be shown how to map a simple one-dimensional tight binding model with a cosine potential in one dimension exactly to a two-dimensional tight binding model with periodic boundary conditions in the presence of a single flux quantum spread evenly on the torus. The mapping is achieved by a partial sequence of “Fast Fourier Transform” (FFT) steps which if completed would be an exact Fourier transform of the original model. Each step of the FFT recursively maps a tight binding model into two decoupled sublattices of half the lattice length.     

Highly selective artificial gel antibodies for detection and quantification of biomarkers in clinical samples. II. Albumin in body fluids of patients with neurological disorders

We have previously used the molecular‐imprinting method for the synthesis of artificial gel antibodies, highly selective for various proteins. In the present work, we have synthesized artificial gel antibodies against human albumin with the aim to develop a simple and rapid procedure to measure the concentration of this protein in samples of clinical interest. The procedure, based on the design of a standard curve (see the preceding paper), was applied on a quantitative analysis of albumin in human plasma and cerebrospinal fluid (CSF). We found that our technique permitted detection of albumin in these body fluids with high precision and that the concentration of this protein was significantly enhanced in CSF from patients with amyotrophic lateral sclerosis (ALS), compared to control samples. This finding is in agreement with results from earlier studies, which confirms the validity of our analysis technique and suggests that the barrier permeability may be affected in ALS, perhaps also for other proteins. No enhancement in plasma levels of albumin was seen in patients with ALS, but rather a decrease. The results further indicate that our approach might also apply well to other biomarkers for the actual neurological disease and other disorders.     

Exact transformation for spin-charge separation of spin-1/2 fermions without constraints

We demonstrate an exact local transformation which maps a purely Fermionic many-body system to a system of spinful bosons and spinless fermions, demonstrating a possible path to a non-Fermi-liquid state. We apply this to the half-filled Hubbard model and show how the transformation maps the ordinary spin half Fermionic degrees of freedom exactly and without introducing Hilbert space constraints to a chargelike quasicharge fermion and a spinlike quasispin Boson while preserving all the symmetries of the model. We present approximate solutions with localized charge which emerge naturally from the Hubbard model in this form. Our results strongly suggest that charge tends to remain localized for large values of the Hubbard U.     

Time-resolved x-ray microscopy of spin-torque-induced magnetic vortex gyration

Time-resolved x-ray microscopy is used to image the influence of alternating high-density currents on the magnetization dynamics of ferromagnetic vortices. Spin-torque-induced vortex gyration is observed in micrometer-sized permalloy squares. The phases of the gyration in structures with different chirality are compared to an analytical model and micromagnetic simulations, considering both alternating spin-polarized currents and the current's Oersted field. In our case the driving force due to spin-transfer torque is about 70% of the total excitation while the remainder originates from the current's Oersted field. This finding has implications to magnetic storage devices using spin-torque driven magnetization switching and domain-wall motion.     

Width dependence of the nonadiabatic spin-transfer torque in narrow domain walls

We analytically determine the spatially varying spin-transfer torque within a domain wall. In the case of ballistic spin and diffusive charge transport, the spin-transfer torque as well as the local degree of nonadiabaticity oscillate within a domain wall. In narrow domain walls, the degree of nonadiabaticity ceases to be a constant material parameter but depends on the domain-wall width including a possible sign change, which is crucial for experiments and the technological utilization in spin-transfer-torque-based storage devices.     

Universal method for synthesis of artificial gel antibodies by the imprinting approach combined with a unique electrophoresis technique for detection of minute structural differences of proteins, viruses, and cells (bacteria). III: gel antibodies against cells (bacteria)

Artificial antibodies in the form of gel granules were synthesized from the monomers acrylamide and N,N'-methylenebisacrylamide by the imprinting method in the presence of Echerichia coli bacteria as template. The electrophoretic migration velocities of the gel antibodies (i) saturated with the antigen (Escherichia coli MRE-600), (ii) freed of the antigen, and (iii) resaturated with bacteria, were determinated by electrophoresis in a rotating narrow-bore tube of 245 mm length and the 2.5 and 9.6 mm inner and outer diameters, respectively. Removal of bacteria from the gel antibodies was made by treatment with enzymes, followed by washing with SDS and buffer. Gel granules becoming charged by adsorption of bacteria move in an electrical field. We obtained a significant selectivity of gel antibodies for E. coli MRE-600, since the granules did not interact with Lactococcus lactis; and when E. coli BL21 bacteria were added to the gels selective for E. coli MRE-600, a significant difference in the migration rate of the complexes formed with the two strains was observed indicating the ability of differentiation between the two strains. The gel antibodies can be used repeatedly. The new imprinting method for the synthesis of artificial gel antibodies against bioparticles described herein, and the classical electrophoretic analysis technique employed, thus represent - when combined - a new approach to distinguish between different types and strains of bacteria. The application area can certainly be extended to cover other classes of cells.