Sawtooth Stimuli Research Articles

Preferential Loss of Contrast Decrement Responses in Human Glaucoma.

PurposeThe purpose of this study was to determine whether glaucoma in human patients produces preferential damage to OFF visual pathways, as suggested by animal experimental models, patient electroretinogram (ERG), and retinal imaging data.MethodsSteady-state visual evoked potentials (SSVEPs) were recorded monocularly from 50 patients with glaucoma and 28 age-similar controls in response to equal Weber contrast increments and decrements presented using 2.73 hertz (Hz) sawtooth temporal waveforms.ResultsThe eyes of patients with glaucoma were separated into mild (better than −6 decibel [dB] mean deviation; n = 28) and moderate to severe (worse than −6 dB mean deviation, n = 22) groups based on their Humphrey 24-2 visual field measurements. Response amplitudes and phases from the two glaucoma-severity groups were compared to controls at the group level. SSVEP amplitudes were depressed in both glaucoma groups, more so in the moderate to severe glaucoma group. The differences between controls and the moderate-severe glaucoma groups were more statistically reliable for decrements than for increments. Mean responses to decremental sawtooth stimuli were larger than those to increments in controls and in the mild glaucoma but not in the moderate to severe glaucoma group at the first harmonic. OFF/decrement responses at the first harmonic were faster in controls, but not in patients.ConclusionsThe observed pattern of preferential loss of decremental responses in human glaucoma is consistent with prior reports of selective damage to OFF retinal ganglion cells in murine models and in data from human ERG and retinal imaging. These data motivate pursuit of SSVEP as a biomarker for glaucoma progression.

Comparison of macaque and human L- and M-cone driven electroretinograms

PurposeThe macaque retina is often used as a model for the human retina. However, there are only a handful of direct in vivo comparisons of the retinal physiology in humans and macaques. In the current study, ERG responses to luminance, L-cone isolating and M-cone isolating stimuli with sinusoidal, sawtooth and square wave temporal profiles were measured. The results were compared with those obtained from human observers. MethodsThe responses from five anesthetized adult macaques were measured. Full field stimuli were created. L- and M-cone isolating stimuli were based on the triple silent substitution technique. Sinusoidal stimuli had temporal frequencies between 4 and 56 Hz in 4 Hz steps. Sawtooth stimuli with rapid-on ramp-off and with rapid-off ramp-on excitation profiles had a frequency of 4 Hz. Square stimuli were presented at 2 Hz. ResultsMacaque and human ERGs in response to L- and M-cone isolating stimuli reflect L/M opponency and luminance activity. In responses to sine waves, cone opponency dominates at low temporal frequencies (4–12 Hz); luminance dominates at high temporal frequencies. The responses to sawtooth and square wave stimuli reflect a mixture of chromatic and luminance activity. L:M response ratios vary between individuals both in macaques and humans. Macaques show more complex responses, including greater second harmonic contributions than those in humans. ConclusionsMacaque and human ERGs share basic underlying mechanisms reflecting L/M opponency and luminance activity. There may be quantitative differences possibly reflecting differences in contributions of inner retinal mechanisms to the ERGs.

Hue shifts produced by temporal asymmetries in chromatic signals.

Observers viewed M- or L-cone-isolating stimuli and compared slowly-on and slowly-off sawtooth waveforms of the same mean chromaticity and luminance. Between 6 and 13 Hz, the mean hue of slowly-on L-cone and slowly-off M-cone sawtooth flicker appeared redder, and the mean hue of slowly-off L-cone and slowly-on M-cone sawtooth stimuli appeared greener-despite all the waveforms' having the same mean, near-yellow-appearing chromaticity. We measured the effect of the modulation depth and the slope of the sawtooth on the mean hue shifts as a function of temporal frequency. The results are complex but show that discriminability depended mainly on the second harmonic of the waveforms. We considered several models with combinations of linear and nonlinear stages. First, we considered models in which a nonlinear stage limits the rate of change of hue and restricts the steep slope of the sawtooth waveform more than its shallow slope, thus shifting the mean hue in the direction of the shallower slope (such a nonlinearity is also known as a slew-rate limit). Second, we considered saturation models in which the nonlinear stage compresses hue signals and thus shifts the mean of asymmetrical waveforms with or without differentiation before the nonlinearity. Overall, our modeling and results suggest that the hue shift occurs at some nonlinear mechanism in the chromatic pathway; and that, in terms of the Fourier components of the various waveforms, the effect of the nonlinearity depends crucially on the timing of the second harmonic relative to the first.

An asymmetric outer retinal response to drifting sawtooth gratings.

Electroretinogram (ERG) studies have demonstrated that the retinal response to temporally modulated fast-ON and fast-OFF sawtooth flicker is asymmetric. The response to spatiotemporal sawtooth stimuli has not yet been investigated. Perceptually, such drifting gratings or diamond plaids shaded in a sawtooth pattern appear brighter when movement produces fast-OFF relative to fast-ON luminance profiles. The neural origins of this illusion remain unclear (although a retinal basis has been suggested). Thus we presented toad eyecups with sequential epochs of sawtooth, sine-wave, and square-wave gratings drifting horizontally across the retina at temporal frequencies of 2.5-20 Hz. All ERGs revealed a sustained direct-current (DC) transtissue potential during drift and a peak at drift offset. The amplitudes of both phenomena increased with temporal frequency. Consistent with the human perceptual experience of sawtooth gratings, the sustained DC potential effect was greater for fast-OFF cf. fast-ON sawtooth. Modeling suggested that the dependence of temporal luminance contrast on stimulus device frame rate contributed to the temporal frequency effects but could not explain the divergence in response amplitudes for the two sawtooth profiles. The difference between fast-ON and fast-OFF sawtooth profiles also remained following pharmacological suppression of postreceptoral activity with tetrodotoxin (TTX), 2-amino-4-phosphonobutric acid (APB), and 2,3 cis-piperidine dicarboxylic acid (PDA). Our results indicate that the DC potential difference originates from asymmetries in the photoreceptoral response to fast-ON and fast-OFF sawtooth profiles, thus pointing to an outer retinal origin for the motion-induced drifting sawtooth brightness illusion.

Full-field electroretinogram response to increment and decrement stimuli.

The d-wave is typically elicited after the termination of an increment flash, but a decrement flash provides an alternative, and perhaps more appropriate, stimulus to elicit the d-wave. Here, we investigated the affects of stimulus polarity on the electroretinogram (ERG) response. ERG responses elicited to increment and decrement flashes of varying intensity and duration from different background levels were measured from human participants to assess the b-wave and d-wave responses as a function of adaptation level and flash polarity. Response amplitudes were measured using standard metrics for waveform analysis. The amplitude of the b-wave is larger than the d-wave regardless of flash polarity when using different background levels which maximized the dynamic range of the two waveforms. However, when response amplitudes are measured from a common background, the d-wave elicited with decrement flash was larger than the b-wave elicited by an increment flash. This trend was evident across a range of background levels. The b-wave and d-wave become separate entities when flash duration reaches approximately 50 ms. Rapid-on and rapid-off sawtooth stimuli were also tested against increment and decrement step stimuli that were matched in mean luminance. These two stimulus types produced different amplitude b-wave and d-wave responses, suggesting asymmetric effects of the two stimulus types on the retinal response. We conclude that the response properties of the b-wave and d-wave are influenced by the duration, polarity and waveform of the stimulus, as well as the background from which the stimuli arise.

Mechanisms of the dimming and brightening aftereffects

Dimming and brightening aftereffects occur after exposure to a temporal luminance sawtooth stimulus: A subsequently presented steady test field appears to become progressively dimmer or brighter, depending on the polarity of the adapting sawtooth. Although described as "dimming" and "brightening," it is plausible that a component of the aftereffects is based on contrast changes rather than on luminance changes. We conducted two experiments to reveal any contrast component. In the first we investigated whether the aftereffects result from the same mechanism that causes a polarity-selective loss in contrast sensitivity following luminance sawtooth adaptation. We manipulated test contrast: If a component of the aftereffect results from a polarity selective loss of contrast sensitivity we would expect that the aftereffects would differ in magnitude depending on the contrast polarity of the test fields. We found no effect of test-field polarity. In the second experiment we used an adapting sawtooth with a polarity consistent in contrast but alternating in luminance in order to induce a potential equivalent aftereffect of contrast. Again, we found no evidence that the aftereffects result from contrast adaptation. In a third experiment, we used S-cone isolating stimuli to discover whether there are S-cone dimming and brightening aftereffects. We found no aftereffects. However, in a fourth experiment we replicated Krauskopf and Zaidi's (1986) finding that adaptation to S-cone sawtooth stimuli affects thresholds for increment and decrement detection. The mechanism underlying the dimming and brightening aftereffects thus seems to be independent of the mechanism underlying the concurrent polarity selective reductions in contrast sensitivity.

Human photopic ON- and OFF-ERG responses elicited by square wave and sawtooth stimuli.

In this study, the on- and off-responses elicited by luminance square wave and sawtooth stimuli at different temporal frequencies and contrasts are described quantitatively. Adding on- and off-responses reveals response asymmetries. Full-field stimuli were produced using a Ganzfeld bowl with arrays of light-emitting diodes (LEDs) as light sources. ERG responses were recorded from six normal subjects. The amplitudes and implicit times of components of the on- and off-responses and the additions were analyzed. The amplitudes of the on-, off- and addition components elicited by square wave stimuli did not depend on temporal frequency with the exception of the late negative components, which decreased with increasing temporal frequency up to 4 Hz. The amplitudes of all components elicited by sawtooth stimuli, except the P-on, decreased with increasing temporal frequency. The amplitude of all components elicited by square wave and sawtooth stimuli were positively correlated with stimulus contrast. The implicit times of the on-components to square wave stimuli and all response components to sawtooth stimuli decreased with increasing temporal frequency. Contrast had an effect on the implicit times of the N-on, P-on, P-off and P-add components elicited by square wave stimuli and the N-on, P-on, P-add and LN-on components elicited by sawtooth stimuli. The asymmetries between on- and off-responses can possibly be used to reveal inner retinal contributions and may therefore be interesting in detecting glaucomatous changes.

Asymmetries in the contributions of On- and Off-mechanisms to the ERG signal.

responses were recorded to rapid-on and rapid-off L- and M-cone isolating sawtooth stimuli of different cone contrasts. In addition, the responses were recorded to simultaneous in-phase stimulation of the L- and M-cones at equal cone contrast. Linear responses to mirror imaged rapid-on and rapid-off sawtooth stimuli are also mirror imaged. By adding on- and off- responses, linear response components will cancel and nonlinearities will remain. Because nonlinearities that occur at a certain stage of visual processing will influence subsequent stages, linear response components will probably have an outer retinal origin and nonlinearities probably originate mainly in the inner (post-receptoral) retina. Keywords: electroretinograms, On- and Off- responses, L- and M-cones, asymmetries.

On- and off-response ERGs elicited by sawtooth stimuli in normal subjects and glaucoma patients

The aim of this study is to measure the on- and off-responses and their response asymmetries elicited by sawtooth stimuli in normal subjects and glaucoma patients. Furthermore, the correlation between the ERGs and other functional and structural parameters are investigated. Full-field stimuli were produced using a Ganzfeld bowl with Light Emitting Diodes (LEDs) as light sources. On- and off-response ERGs were recorded from 17 healthy subjects, 12 pre-perimetric and 15 perimetric glaucoma patients using 4-Hz luminance rapid-on and rapid-off sawtooth stimuli (white light; mean luminance 55 cd/m(2)) at 100% contrast. The on- and off-responses were added to study response asymmetries. In addition, flash ERGs were elicited by red stimuli (200 cd/m(2)) on a blue background (10 cd/m(2)). The mean deviations (MD) of the visual field defects were obtained by standard automated perimetry. The retinal nerve fibre layer thickness (RNFLT) was measured with Spectral Domain Optical Coherence Tomography (SOCT). We studied the correlation between ERG response amplitudes, visual field mean deviation (MDs) and RNFLT values. The on-responses showed an initial negative (N-on) followed by a positive (P-on), a late positive (LP-on) and a late negative responses (LN-on). The off-responses showed an initial positive (P-off) a late positive (LP-off) and a late negative response (LN-off). The addition of on- and off-responses revealed an initial positive (P-add) and a late negative response (LN-add). The on-response components (N-on, P-on and LN-on) in the glaucoma patients were relatively similar to those of the control subjects. However, the LP-on was significantly elevated (p = 0.03) in perimetric patients. The LP-off was significantly elevated (p < 0.001), and the amplitude of LN-off was significantly reduced in perimetric patients (p = 0.02). The LN-add amplitude was significantly reduced (p < 0.001) and delayed (p = 0.03) in perimetric patients. The amplitudes of the LN-off and LN-add ERG components were significantly correlated with the PhNR in the flash ERG (LN-off: p = 0.01; LN-add: p < 0.001) and with RNFLT (LN-off: p = 0.006; LN-add: p = 0.001). On- and off-response ERGs and their response asymmetries, elicited by sawtooth stimuli, are altered in the glaucoma patients. The late components are affected. Changes in the late negative components are correlated with structural and other functional changes.

Spatial distributions of on- and off-responses determined with the multifocal ERG

We studied the contribution of retinal on and off-mechanisms in the multifocal electroretinogram (mfERG) by measuring responses to saw tooth stimuli. Six healthy subjects participated in this study. Rapid-on and rapid-off sawtooth stimuli with a period of 427 ms were presented in a multifocal pattern composed of 19 hexagons. The stimuli were interleaved with a blank field of the mean luminance and chromaticity. On- and off-responses were added to extract response asymmetries. The amplitudes of on-, off-, and added-responses were determined for different eccentricities relative to a signal baseline that was defined as the average of the electrical level recorded in two different time windows in which no responses were present. Measurements were repeated with eight different stimulus stretch factors to account for changes in retinal cell density as a function of eccentricity. The amplitudes of all ERG components decreased with increasing eccentricity for all stretch factors. For stretch factors between 0 and 20, responses to the central and immediately adjacent hexagons were large in amplitude. For more peripheral hexagons, the responses were very small or absent. Three components were identified in the on-responses (N20(on), P46(on) and N100(on)). In the offresponses, we found one positive (P20(off)) and one negative (N90(off)) component, whereas in the addition, three components (N20(add), P46(add) and N100(add)) could be observed. The N20(on) and P46(on) amplitudes decreased less steeply with eccentricity than the N100(on) amplitude, whilst the P20(off) and N90(off) amplitudes exhibited a similar decrease with eccentricity. In the addition, the two negative components exhibited a similar decrease in amplitude as a function of eccentricity and decreased more steeply than the positive component. The number of stimulated cones and retinal ganglion cells was estimated from anatomical data and compared with the responses. The spatial properties of the amplitudes of N20(on), P46(on), P20(off), and N90(off) and P46(add) were similar to those of the stimulated cone numbers. The remaining components had spatial characteristics that resembled those of the retinal ganglion cells. It is proposed that the ERG asymmetries revealed in the summed responses have post-receptoral origins, some of them reflecting the activity of the ganglion cell population. The use of sawtooth stimuli provide, similar to the pattern ERG, a way to record the ERG asymmetries.

Representation of Time-Varying Stimuli by a Network Exhibiting Oscillations on a Faster Time Scale

Sensory processing is associated with gamma frequency oscillations (30–80 Hz) in sensory cortices. This raises the question whether gamma oscillations can be directly involved in the representation of time-varying stimuli, including stimuli whose time scale is longer than a gamma cycle. We are interested in the ability of the system to reliably distinguish different stimuli while being robust to stimulus variations such as uniform time-warp. We address this issue with a dynamical model of spiking neurons and study the response to an asymmetric sawtooth input current over a range of shape parameters. These parameters describe how fast the input current rises and falls in time. Our network consists of inhibitory and excitatory populations that are sufficient for generating oscillations in the gamma range. The oscillations period is about one-third of the stimulus duration. Embedded in this network is a subpopulation of excitatory cells that respond to the sawtooth stimulus and a subpopulation of cells that respond to an onset cue. The intrinsic gamma oscillations generate a temporally sparse code for the external stimuli. In this code, an excitatory cell may fire a single spike during a gamma cycle, depending on its tuning properties and on the temporal structure of the specific input; the identity of the stimulus is coded by the list of excitatory cells that fire during each cycle. We quantify the properties of this representation in a series of simulations and show that the sparseness of the code makes it robust to uniform warping of the time scale. We find that resetting of the oscillation phase at stimulus onset is important for a reliable representation of the stimulus and that there is a tradeoff between the resolution of the neural representation of the stimulus and robustness to time-warp.

Adaptation of spatiotemporal mechanisms by increment and decrement stimuli.

Sawtooth modulation has been used in the past to examine visual sensitivity to luminance increments and decrements. The threshold elevation caused by adaptation depends on the spatial profile of the stimulus field and the polarities of the adaptation and test stimuli. We hypothesized that the adaptation effects reflect a change in the sensitivity of the spatiotemporal channels that detect the stimuli. We used a 2-deg disk centered in a larger surround field. Five levels of contrast between the test field and surround were investigated: equiluminant, three intermediate levels, and dark. At each contrast, observers adapted for 5 s to 2-Hz sawtooth modulation (rapid-on or rapid-off). Immediately after adaptation, thresholds were measured for detection of a single cycle of either a rapid-on or a rapid-off waveform. Varying the contrast of the surround affected observers' sensitivity to the polarity of the sawtooth stimulus to the extent that the pattern of sensitivity with the equiluminant surround was the opposite of that with the dark surround. To examine temporal factors, we measured thresholds for slow (500-ms ramps) and fast (8.3-ms pulses) test stimuli. The adaptation effect was preserved with the ramp stimuli but not with the pulse stimuli. Blurring the edge between the test and surround fields in the equiluminant surround condition raised thresholds for all sawtooth test stimuli, suggesting that spatiotemporal channels sensitive to high spatial frequencies and low temporal frequencies facilitate detection in that condition. These findings suggest that adaptation to sawtooth modulation can differentially effect the sensitivity of ON and OFF pathways, but the relative desensitization of each pathway depends on an interaction with the adaptation state of spatiotemporal channels that are involved in detection.

Processing of scotopic increments and decrements.

Rod and cone photoreceptors send their signals to ON- and OFF-retinal ganglion cells through different pathways in the primate retina. We hypothesized that increments and decrements of light may be processed differently by the rod-bipolar pathway because of the funneling of the rod signal through the rod bipolar cell. We tested this hypothesis using a psychophysical adaptation paradigm, which has provided evidence that photopic increments and decrements of light are processed by ON- and OFF-pathways in the human visual system. We had observers adapt to either a rapid-on or rapid-off sawtooth waveform, under both photopic and scotopic conditions. We then measured detection thresholds for one cycle of a rapid-on or rapid-off sawtooth stimulus. For photopic stimuli, sawtooth adaptation asymmetrically raised thresholds for test stimuli in a manner that depended on the polarity of the adaptation stimulus. For scotopic stimuli, thresholds were raised, but no significant selective adaptation effect was found. By repeating the photopic condition with sawtooth stimuli which had been filtered using an impulse response function derived for the rod system, we demonstrated that the lack of selective adaptation was not a consequence of the sluggish temporal response of the rod-bipolar pathway. We conclude instead that the reduced effectiveness of sawtooth adaptation is due to channeling of rod photoreceptor signals through the rod bipolar cell before reaching ON- and OFF-ganglion cells.

An electrophysiological metric of activity within the ON- and OFF-pathways in humans.

Several animal studies have shown an anatomical and functional separation between the ON- and OFF-pathways in the retina and in the lateral geniculate nucleus. Psychophysical studies in humans have also documented separate pathways that process increments and decrements of light. However, at the level of the visual cortex, there is electrophysiological evidence of interactions between the ON- and OFF-pathways. In addition, psychophysical studies have shown that these pathways can exhibit differential sensitivity and be differentially adapted. These findings motivated an electrophysiological study to gather further evidence of processing within the ON- and OFF-pathways in the human visual system. Using sawtooth stimulus modulation, we measured the visual evoked potential (VEP) before and after adaptation to both rapid-on and rapid-off sawtooth stimuli. The effect of adaptation was determined by comparing the VEP response in three test conditions: without adaptation, after adaptation to the same sawtooth polarity, and after adaptation to the opposite sawtooth polarity. The results reveal a selective adaptation effect, which provides physiological evidence for separate processing of increments and decrements in the human visual system. We conclude that with appropriate stimulus parameters, the VEP can serve as an objective measure of processing within the ON- and OFF-pathways in humans.

Effect of sawtooth polarity on chromatic and luminance detection.

Psychophysical studies have documented that many observers show lower thresholds for rapid-off than for rapid-on sawtooth luminance modulation. This finding, together with physiological findings from chromatically opponent ganglion cells of the macaque monkey, prompted a search for a similar bias in psychophysical detection of chromatic increments and decrements of light. Using a luminance pedestal in conjunction with a luminance background to favor detection by chromatic mechanisms, we measured spectral sensitivity for rapid-on and rapid-off sawtooth stimuli presented spatially coextensive with the pedestal. There were two different pedestal chromaticities: one broadband, and the second composed only of long-wavelength light to enhance short-wavelength-sensitive, cone-mediated detection. Spectral-sensitivity measurements for different wavelength stimuli revealed no systematic differences across the visible spectrum as a function of sawtooth waveform polarity or pedestal chromaticity. Similarly, temporal contrast-sensitivity functions for hetero-chromatically modulated red-green sawtooth stimuli did not reveal an asymmetry in sensitivity for rapid-red and rapid-green chromatic change. Some of the observers showed a higher sensitivity for luminance modulated rapid-off sawtooth stimuli, as also noted in previous studies. This asymmetry was not found when a white luminance pedestal and background was used. These results suggest that the cone inputs to chromatically opponent ON- and OFF-center cells are sufficiently balanced to provide equivalent psychophysical thresholds for chromatic increments and decrements of light.

Jamming Avoidance in the Electric Fish Eigenmannia: Harmonic Analysis of Sexually Dimorphic Waves

ABSTRACT The present report shows an intraspecific, sexually dimorphic variation in harmonic content and waveform, as well as intensity, of the Electric Organ Discharges (EODs) in the green knife fish, Eigenmannia (Figs 2, 11). There is a close correlation between harmonic content of the EODs and waveform (as defined by the ratio of intervals between zero-crossings in the two half-waves of one EOD cycle; Fig. 3). The aim of the following experiments was to determine whether the fish are sensitive to differences in stimulus waveform or harmonic content. Stimulation with electric fields of various waveforms but equal peak-to-peak amplitudes at frequencies close to the fish’s frequency elicited the Jamming Avoidance Response (JAR) which is an EOD frequency change increasing the frequency difference (Watanabe &amp; Takeda, 1963). The strength of JARs to distorted square wave and sawtooth stimuli was 25% smaller than that elicited by sine wave stimuli (Fig. 6). Undistorted square waves elicited stronger responses than sine waves, while undistorted sawtooth waves were the least effective (Table 1). The differences in response strength were proportional to differences in the intensity of the fundamental frequency or first harmonic, fi, of the stimulus waveforms. Subharmonic stimuli of nine artificial or synthesized natural waveforms at frequencies near one-half or one-third of the EOD resting frequency elicited responses only when a strong higher harmonic, or overtone, of the stimulus was close to the EOD fundamental frequency (Fig. 7). Stimuli of different waveforms, but identical spectral amplitudes, elicited similar responses not significantly different from each other, at stimulus frequencies near one-half (Table 3) and near the EOD resting frequency (Fig. 10). Eigenmannta’s JARs to synthesized male EODs at frequencies close to the fish’s frequency were weaker than those to female EODs of equal peak-to-peak amplitude. The weaker response was proportional to the weaker intensity of the first harmonic of the male EOD (Fig. 12). A stimulus frequency near one-half of the EOD baseline frequency evoked opposite results, as the second harmonic, f2, of the male EOD was relatively four times stronger than that of the female EOD (Table 4). Eigenmannia responded to jamming signals as if it performed a limited spectral amplitude (Fourier) analysis, determining the intensity of that stimulus harmonic (at least up to the third) enclosed within a narrow frequency band centred on its own EOD fundamental frequency. The assessment of that harmonic was independent of stimulus waveform, peak-to-peak amplitude, or power, demonstrating linear filtering of the stimulus wave. Because of Eigenmannia’s sensitivity to the harmonic content of the stimulus wave, as also demonstrated in subharmonic experiments, the natural variation of EODs in harmonic content may serve in species and mate recognition.

Sinusoidal plucks and bows are not categorically perceived, either

Cutting and Rosner (Perception & Psychophysics, 1974,16, 564–570) reported that two acoustic nonspeech continua varying in rise time were categorically perceived. We have already shown (Rosen & Howell,Perception & Psychophysics, 1981,30, 156–168) that the reason their sawtooth continuum was perceived in such a way, and in particular why it exhibited a midcontinuum peak in the discrimination function, was entirely due to the stimuli not having the intended rise times. The other nonspeech continuum that varied in rise time and was reported to be categorically perceived used a sinusoidal carrier. Although the labeling functions obtained were not as sharp as those obtained with sawtooth stimuli, the characteristic midcontinuum discrimination peak was found. We generated such a set of sinusoidal stimuli and found no evidence of categorical perception. Just as we have previously found for sawtooth stimuli, discrimination is best at the short rise-time end of the continuum and decreases monotonically with increasing rise time.

Categorical perception of nonspeech sounds by 2-month-old infants

According to recent investigations, adult listeners perceive rise-time differences in both speech and nonspeech stimuli in a categorical manner (Cutting & Rosner, 1974). Adults labeled sawtooth-wave stimuli as either plucked or bowed. The present study uses the high-amplitude sucking technique to explore the 2-month-old infant’s perception of rise-time differences for sawtooth stimuli. Infants discriminated rise-time differences which marked off the different nonspeech categories, but did not discriminate equal differences within either category. Thus, the present study shows that infants, like adults, can perceive nonspeech stimuli in a categorical manner.

Perceptual categories for musiclike sounds: implications for theories of speech perception.

Sawtooth acoustic stimuli of different rise times are identified as coming from a plucked string instrument (pluck) or a bowed one (bow). Like stop consonants, these sounds are perceived categorically—discrimination is poor for stimuli identified as belonging to a single class but good for those identified as members of different classes. Varying the interval between two successive musiclike stimuli hardly alters discrimination. Sawtooth stimuli lasting 750 ms are clearly perceived categorically; those lasting 250 ms are not. Prolonged exposure to a pluck or bow stimulus can shift the rise-time boundary between categories. Shifts due to such selective adaptation decrease as adapting and test stimuli share fewer characteristics. Adaptation of postulated “feature detectors” therefore may occur in input systems prior to the detectors themselves. Our findings contradict previous claims that categorical perception and selective adaptation are manifestations of psychological processes unique to speech perception.