Confusion effects with sinusoidal and narrow-band noise forward maskers

In some forward-masking conditions, signal thresholds may be elevated by the listener's inability to distinguish the signal from the preceding masker. In this study, such "confusion" effects are investigated for both sinusoidal and narrow-band noise forward maskers combined with sinusoidal signals of varying duration. Results for the sinusoidal maskers show effects of off-frequency listening for brief signals and possibly small effects of confusion for longer signals. Results for the narrow-band noise maskers show a marked influence of confusion over a wide range of signal durations. This range is in good agreement with that predicted from previous work with "pulsing" maskers [D. Neff, J. Acoust. Soc. Am. 78, 1966-1976 (1985)]. These results suggest that studies using narrow-band noise forward maskers or studies of psychophysical suppression should include direct tests for confusion effects in key conditions.     

Sourcing archaeological obsidian by an abbreviated NAA procedure

An abbreviated NAA procedure has been developed to fingerprint obsidian artifacts in the Mesoamerican region. Despite the large number of available sources, an NAA procedure, which relies on producing short-lived isotopes, has been applied with a success rate greater than 90 percent. The abbreviated NAA procedure is rapid and cost competitive with the XRF technique more often applied in obsidian sourcing. Results from the analysis of over 1,200 obsidian artifacts from throughout Mesoamerica are presented.     

Additivity of forward masking

Masked thresholds for a 1000-Hz sinusoidal signal were measured as a function of masker level in both forward and simultaneous masking for two types of maskers: a 1000-Hz sinusoid and a narrowband noise, 60-Hz wide, centered at 1000 Hz. In forward masking, the noise masker produced much steeper growth-of-masking functions than the sinusoid. Presenting a contralateral broadband noise "cue" with the forward masker dramatically reduced the slope of masking for the noise masker but did not influence results for the sinusoidal masker. The noise remained the more effective masker. The amount of masking produced by combinations of equally effective narrowband-noise and sinusoidal maskers was compared to that produced by each masker individually with and without the contralateral cue. No additional masking beyond that predicted by energy summation was measured for forward masking. Additional masking beyond energy-sum predictions was measured for analogous conditions in simultaneous masking. Comparisons of results obtained with and without the contralateral cue suggest that signal thresholds in the presence of narrowband-noise forward maskers can reflect nonperipheral auditory processes.     

A New Total Synthesis of D-threo-L-talo-Octose

A new approach to the total, asymmetric synthesis of D -threo-L -talo-octose ((?)- 1 ) and its derivatives is presented. It is based on the chemoselective Wittig-Horner monoolefination of a 5-deoxy-D -ribo-hexodialdose derivative 4 obtained by selective reduction of (?)-5-deoxy-2.3-O-isopropylidene-/β-D -ribo-hexofuranurono-6,1-lactone ((?)- 3 ). Allylic bromination of the resulting methyl (E)-oct-6-enofuranuronate (+)- 5 followed by intramolecular nucleophilic displacement of the so-obtained bromides gave a 13.3:1 mixture of (?)-methyl (E)-l,4-anhydro-6,7-dideoxy-2,3-O-isopropylidene-β-L -talo-oct-6-enopyranuronate ((?)- 8 ) and methyl (E)-l,4-anhydro-6,7-dideoxy-2,3-O-isopropylidene-α-D -allo-oct-6-enopyranuronate ( 9 ). The double hydroxylation of the enoate (?)- 8 followed Kishi's rule and gave the corresponding D -threo-β-L -talo-octopyranuronate derivative (?)- 11 with a good diastereoselectivity. Reduction of ester (?)- 11 and deprotection led to pure (?)- 1 .     

Experimental and Computational Study of the Thermal Decomposition of 3‐Methyl‐3‐buten‐1‐ol in m‐Xylene Solution

An experimental study of the thermal decomposition of a β‐hydroxy alkene, 3‐methyl‐3‐buten‐1‐ol, in m‐xylene solution, has been carried out at five different temperatures in the range of 513.15–563.15 K. The temperature dependence of the rate constants for the decomposition of this compound in the corresponding Arrhenius equation is given by ln k (s^?1) = (25.65 ± 1.52) ? (17,944 ± 814) (kJ·mol^?1)·T^?1. A computational study has been carried out at the M05–2X/6–31+G(d,p) level of theory to calculate the rate constants and the activation parameters by the classical transition state theory. There is a good agreement between the experimental and calculated rate constants and activation Gibbs energies. The bonding characteristics of reactant, transition state, and products have been investigated by the natural bond orbital analysis, which provides the natural atomic charges and the Wiberg bond indices. Based on the results obtained, the mechanism proposed is a one‐step process proceeding through a six‐membered cyclic transition state, being a concerted and slightly asynchronous process. The results have been compared with those obtained previously by us (Struct Chem 2013, 24, 1811–1816) for the thermal decomposition of 3‐buten‐1‐ol, in m‐xylene solution. We can conclude that in the compound studied in this work, 3‐methyl‐3‐buten‐1‐ol, the effect of substitution at position 3 by a weakly activating CH₃ group is the stabilization of the transition state formed in the reaction and therefore a small increase in the rate of thermal decomposition.     

Structural and Kinetic Aspects of Blood Plasma Protein Adsorption on the Surface of Hydrophobic Polymers

Abstract

Due to the wide use of polymers in medicine, researchers are required to solve a very important problem–to understand the interaction between materials of nonphysiological origin and the surrounding biological liquids, and tissues, particularly blood.