Number Of Modulation Cycles Research Articles

Detection of vertical interocular phase disparities using luster as cue.

Interocular disparities in contrast generate an impression of binocular luster, providing a cue for their detection. Disparities in the carrier spatial phase of horizontally oriented Gabor patches also generate an impression of luster, so the question arises as to whether it is the disparities in local contrast that accompany the phase disparities that give rise to the luster. We examined this idea by comparing the detection of interocular spatial phase disparities with that of interocular contrast disparities in Gabor patches, in the latter case that differed in overall contrast rather than phase between the eyes. When bandwidth was held constant and Gabor spatial frequency was varied, the detection of phase and contrast disparities followed a similar pattern. However, when spatial frequency was fixed and Gabor envelope standard deviation (and hence number of modulation cycles) was varied, thresholds for detecting phase disparities followed a U-shaped function of Gabor standard deviation, whereas thresholds for contrast disparities, following an initial decline, were more-or-less constant as a function of Gabor standard deviation. After reviewing a number of possible explanations for the U-shape found with phase disparities, we suggest that the likely cause is binocular sensory fusion, the strength of which increases with the number of modulation cycles. Binocular sensory fusion would operate to reduce phase but not contrast disparities, thus selectively elevating phase disparity thresholds.

Temporal integration of monaural and dichotic frequency modulation.

Frequency modulation (FM) detection at low modulation frequencies is commonly used as an index of temporal fine-structure processing. The present study evaluated the rate of improvement in monaural and dichotic FM across a range of test parameters. In experiment I, dichotic and monaural FM detection was measured as a function of duration and modulator starting phase. Dichotic FM thresholds were lower than monaural FM thresholds and the modulator starting phase had no effect on detection. Experiment II measured monaural FM detection for signals that differed in modulation rate and duration such that the improvement with duration in seconds (carrier) or cycles (modulator) was compared. Monaural FM detection improved monotonically with the number of modulation cycles, suggesting that the modulator is extracted prior to detection. Experiment III measured dichotic FM detection for shorter signal durations to test the hypothesis that dichotic FM relies primarily on the signal onset. The rate of improvement decreased as duration increased, which is consistent with the use of primarily onset cues for the detection of dichotic FM. These results establish that improvement with duration occurs as a function of the modulation cycles at a rate consistent with the independent-samples model for monaural FM, but later cycles contribute less to detection in dichotic FM.

Sensorineural hearing loss enhances auditory sensitivity and temporal integration for amplitude modulation.

Amplitude-modulation detection thresholds (AMDTs) were measured at 40 dB sensation level for listeners with mild-to-moderate sensorineural hearing loss (age: 50-64 yr) for a carrier frequency of 500 Hz and rates of 2 and 20 Hz. The number of modulation cycles, N, varied between two and nine. The data were compared with AMDTs measured for young and older normal-hearing listeners [Wallaert, Moore, and Lorenzi (2016). J. Acoust. Soc. Am. 139, 3088-3096]. As for normal-hearing listeners, AMDTs were lower for the 2-Hz than for the 20-Hz rate, and AMDTs decreased with increasing N. AMDTs were lower for hearing-impaired listeners than for normal-hearing listeners, and the effect of increasing N was greater for hearing-impaired listeners. A computational model based on the modulation-filterbank concept and a template-matching decision strategy was developed to account for the data. The psychophysical and simulation data suggest that the loss of amplitude compression in the impaired cochlea is mainly responsible for the enhanced sensitivity and temporal integration of temporal envelope cues found for hearing-impaired listeners. The data also suggest that, for AM detection, cochlear damage is associated with increased internal noise, but preserved short-term memory and decision mechanisms.

Temporal integration functions of amplitude modulation depth discrimination: can multiple-looks model explain this

Lee and Bacon (1994) applied a multiple looks model (Viemeister and Wakefield, 1990) as a mechanism of AM depth discrimination when the carrier and the modulator were presented at the same time (gated condition). The model provided a reasonable prediction, but the performance (d') was underpredicted when the number of modulation cycles changed from two to four. They speculated that onset information loss due to gating with two modulation cycles lead to a greater improvement with four modulation cycles. Following this, one would expect that AM depth discrimination can be better predicted by the multiple-looks model for the condition where there is no loss of modulation information at onset. This study compared psychometric functions of AM depth discrimination with different modulation cycles for the gated and onset-only conditions (carrier was presented for 250 ms prior to the modulation to preserve onset information). The slop of the psychometric functions with two modulation cycles was shallower than those with greater modulation cycles for the gated condition, while the slop of the psychometric functions was similar for all modulation cycles for the onset-only condition. The data will be discussed with multiple looks model. [This work was supported by NIDCD Grant No. R03 DC06605-02.]

Discrimination of sinusoidally frequency-modulated sound signals mimicking species-specific communication calls in the FM-bat Phyllostomus discolor.

In the lesser spear-nosed bat, Phyllostomus discolor, maternal directive calls are characterized by an individual type of sinusoidal frequency modulation (= SFM) pattern. Beside modulation frequency, modulation depth, carrier frequency, and number of modulation cycles per call contribute to the mother's vocal signature. Since juvenile P. discolor learn to adapt their isolation calls to the corresponding call characteristics of the own mother or even to playback of a computer-stored directive call, if hand-reared in the absence of conspecifics, the bats' auditory system ought to be able to resolve interindividual differences in communication call structure. However, quantitative psychoacoustic data on the discrimination of SFM signals in this species are not available. Thus, in the present study, lesser spear-nosed bats were trained in a two-alternative forced-choice procedure to discriminate between two alternatingly presented SFM sound signals differing in modulation frequency. Other characteristics of acoustic stimuli were identical and designed to mimick the fundamental of species-specific calls. By gradually reducing the difference in modulation frequency between both stimuli within the behavioural relevant range until the animals' performance dropped below the 75%-correct level, a considerable auditory spectro-temporal resolution has been revealed. Particularly in comparison to the overall interindividual variation of this call parameter (minimal modulation frequency = 49 Hz, maximum = 100 Hz), the determined average difference limen for modulation frequency of 2.42 +/- 0.29 Hz seems substantial and sufficient for labelling individuals.