Effects of flanking band proximity, number, and modulation pattern on comodulation masking release

Comodulation masking release for a 700-Hz pure-tone signal was investigated as a function of the number and spectral positions of 20-Hz-wide comodulated flanking bands. In the first experiment, all stimuli were presented diotically. CMR was examined as a function of the number of flanking bands present, in conditions where the bands were arranged symmetrically around the signal frequency, were below the signal frequency, or were above the signal frequency. The number of flanking bands ranged from one to eight, and the magnitude of the diotic CMR ranged from approximately 5-16 dB. The results indicated: (1) bands closer to the signal resulted in larger masking release, and (2) more bands gave rise to larger CMR (but with diminishing returns above two flanking bands). Two additional sets of diotic conditions were examined and compared to the condition where all eight comodulated flanking bands were present: In one set of conditions, two of the eight flanking bands were removed; in the other set of conditions, two of the eight flanking bands were replaced with bands (termed "deviant" bands) that were not comodulated with respect to the other bands. There was very little effect of reducing eight bands to six, even when the removed bands were relatively near the signal frequency; however, CMR was substantially reduced when deviant bands were introduced, particularly when the deviant bands were placed relatively near the signal frequency. These reductions in CMR were slightly greater when each of the deviant bands had a unique modulation pattern (bideviant bands) than when the two deviant bands themselves shared the same modulation pattern (codeviant bands). In the second experiment, dichotic conditions were examined where the number and spectral positions of the flanking bands in the nonsignal ear were varied (the signal ear received only a 20-Hz-wide noise band centered on the signal frequency). The magnitude of the dichotic CMR ranged from approximately 2-10 dB, depending on condition. Effects of proximity and the number of flanking bands were similar to the effects obtained in diotic conditions. For both the diotic and the dichotic data, the effects of proximity were more consistent with an interpretation based upon across-channel processing than upon a within-channel interaction. The results obtained using deviant bands indicate that it is difficult for the auditory system to disregard the modulation pattern of flanking bands that differ from the modulation pattern of the on-signal band, particularly if such bands are proximal to the signal frequency.     

Comodulation masking release and auditory grouping

The detectability of a pure-tone signal masked by a band of noise centered on the signal can be improved by the addition of flanking noise bands, provided that the temporal envelopes of the flanking bands are correlated with that of the on-signal band. This phenomenon is referred to as comodulation masking release (CMR). The present study examined CMR in conditions in which some flanking noise bands were comodulated with the on-signal band, but other flanking bands (termed "deviant" bands) were not. Past research has indicated that CMR is often substantially reduced when deviant bands are present at spectral locations close to the signal frequency. An investigation was undertaken to determine whether the disruptive effects of such bands could be reduced by factors related to auditory grouping. The signal frequency was 100 Hz. In one condition, only 20-Hz-wide comodulated bands, centered on 400, 600, 800, 1000, 1200, 1400, and 1600 Hz, were present. The CMR for this condition, referenced to threshold for the on-signal band only, was approximately 15 dB. In a second condition, two deviant bands were added at 900 and 1100 Hz; their presence reduced the CMR to only 3-4 dB. The number of deviant bands was then increased progressively, from two to eight bands. Deviant bands either shared a common envelope (codeviant), or had unique envelopes (multideviant). The number of bands that were comodulated with the on-signal band was held constant at six.(ABSTRACT TRUNCATED AT 250 WORDS)     

Immobilizing a Fluorescent Dye Offers Potential to Investigate the Glass/Resin Interface

Silane coupling agents are commonly applied to glass fibers to promote fiber/resin adhesion and enhance durability in composite parts. In this study, a coupling agent multilayer on glass was doped with trace levels of the dimethylaminonitrostilbene (DMANS) fluorophore. The fluorophore was immobilized on the glass surface by tethering the molecule to a triethoxy silane coupling agent, creating the DMANS/silane coupling agent molecule (DMSCA). DMSCA was then diluted with commonly used coupling agents and grafted to a glass microscope coverslip to create a model composite interface. A 53-nm blue shift in fluorescence from the immobilized DMSCA can be followed during cure of an epoxy resin overlayer, giving this technique potential to monitor the properties of the fiber/resin interface during composite processing. Contact angle measurements on these coupling agent layers were similar in the presence or absence of the DMSCA molecule, suggesting that trace levels of the fluorescent probe did not affect the structure of the layer. The immobilized DMSCA molecule behaved similarly to the DMANS precursor in solution. Both showed longer wavelength fluorescence in more polar environments. Copyright 2000 Academic Press.     

(Z)-3-p-tolylsulfinylacrylonitrile as a chiral dienophile: diels-alder reactions with furan and acyclic dienes

The behavior of (Z)-3-p-tolylsulfinylacrylonitrile (1) as a chiral dienophile has been evaluated from its reactions with furan and acyclic dienes. Electrostatic interactions of the cyano group with the sulfinyl one restrict the conformational mobility around the C-S bond, thus controlling the pi-facial selectivity, which is almost complete in all cases, the approach of the diene from the less-hindered face of the dienophile (that bearing the lone electron pair) in the predominant rotamer being the favored one. The regioselectivity is also completely controlled by the cyano group. Additionally, the reactivity of compound 1 as well as its endo-selectivity are both higher than those observed for the corresponding (Z)-3-sulfinylacrylates, thus proving the potential of sulfinylnitriles as chiral dienophiles.     

Solid-Phase Synthesis of a Monofunctional trans-a(2)Pt(II) Complex Tethered to a Single-Stranded Oligonucleotide

Cross-linking ability is possible with the oligonucleotide-tethered, monofunctional trans-Pt(II) complex shown. It was synthesized by a novel solid-phase approach comprising conjugation of immobilized tetrathymidylic acid with a trans-a(2)Pt(II) building unit, ammonolysis, and transformation of the resulting complex (R=1-N-cyclohexylmethylthyminate) into the chloro derivative (R=Cl). a=NH(2)CH(3), T=thymine.