Recovery from adaptation as a function of stimulus orientation

These experiments examined the oblique effect in an adaptation paradigm. Reaction times (RT) to the presence of a grating test stimulus were obtained following adaptation to either a blank field or a grating of the same orientation as the test stimulus. Horizontal, vertical, and oblique test and adaptation orientations were employed. Test gratings were presented at several interstimulus intervals following offset of the adaptation stimulus. RTs following grating adaptation were elevated to a greater extent (relative to blank adaptation) for oblique then for horizontal or vertical stimuli, for two grating spatial frequencies. Differences in RT can be related to differences in sensitivity among channels responsible for detection of the various orientations.

     

Evidence for a common motion mechanism of luminance-modulated and contrast-modulated patterns: selective adaptation.

Selective adaptation effects were measured with contrast-modulated patterns and sine-wave gratings in order to determine the extent to which the two patterns are processed by common mechanisms. Direction-specific adaptation effects were measured for a contrast-modulated adapting pattern and a test pattern. The contrast-modulated adapting pattern was composed of a sine-wave grating of 8 cycles deg-1 whose contrast was spatially modulated by a sinusoid of 1 cycle deg-1 at one of four levels: 100%, 60%, 30%, or 0%. The results showed that contrast-modulation thresholds for contrast-modulated gratings were raised by 0.3 to 0.5 log units following adaptation to a contrast-modulated grating moving in the same direction as the test pattern, relative to thresholds obtained following adaptation to a contrast-modulated grafting moving in the opposite direction. Cross-adaptation effects were also measured with a sine-wave adapting pattern and a contrast-modulated test pattern. The sine-wave adapting pattern was a sine-wave grating of 1 cycle deg-1 whose contrast was set to one of three levels: 16.4%, 1.25%, or 0%. The contrast-modulated test pattern was a sine-wave grating of 8 cycles deg-1 whose contrast was modulated by a sinusoid of 1 cycle deg-1. The results revealed that contrast-modulation thresholds for contrast-modulated gratings were raised by approximately 0.25 log units following adaptation to moving sine-wave gratings, relative to thresholds obtained following adaptation to a uniform field. Cross-adaptation effects were also obtained with a contrast-modulated adapting pattern and a sine-wave test pattern. The results support the view that signals generated from luminance-domain stimuli and from contrast-domain stimuli are processed by a common motion mechanism.     

Laterality differences in sensitivity to line orientation as a function of adaptation duration

Since available evidence indicates that the two cerebral hemispheres are differentially sensitive to different types of stimulus information, and that they also utilize different strategies in processing information, is it possible that the two hemispheres are differentially sensitive to adaptation? Three groups of four subjects each were adapted to black and white gratings using three adapting durations: 500, 1,000, and 5,000 msec. Immediately following adaptation, a test grating was presented in either the left or right visual field. The task of the subject was to determine whether the lines of the adapting and test gratings had the same orientation or not. Analysis showed that in the 5,000-msec and 1,000-msec conditions, more errors occurred with left visual field presentations, responses to left visual field presentations took longer, and a bias-free measure showed that subjects were more sensitive to right visual field presentations. For the 500-msec group, there were no apparent differences between left and right visual fields presentations. The results indicate differential effects of adaptation on the two hemispheres, suggesting sensitivity differences between the two halves of the brain.     

Adaptation effects in facial expression recognition

The effect of adaptation on facial expression recognition was investigated by measuring how identification performance of test stimuli falling along a particular expression continuum was affected after adapting to various prototype emotional faces or a control pattern. The results showed that for recognition of fear, happiness, and sadness, inhibition effects were observed on recognition of test expressions following 5 s adaptation to the same emotion, suggesting different neural populations tuned for the encoding of fearful, happy, and sad expressions. Facilitation of recognition of test stimuli differing in emotion to the adapting stimulus was also sometimes observed. The nature of these adaptation effects was investigated by introducing a size transformation or a delay between adapting and test stimuli and was found to survive these changes. The results of a further experiment argued against a criterion effect being the major source by demonstrating the importance of adapting time in generating the effects. Overall, the present study demonstrates the utility of adaptation effects for revealing functional characteristics of facial expression processing.     

Feature analyzers for the phonetic dimensionstop vs. continuant

Perception of sounds along the phonetic dimensionstop vs. continuant was studied by means of a selective adaptation procedure. Subjects first identified a series of synthetic consonant-vowel syllables whose formant transitions varied in duration, slope, and amplitude characteristics. They were perceived as either [ba] or [wa]. After the initial identification test, an adapting stimulus was presented repeatedly, and then the subjects again identified the original test series. Adapting with a stop (either [ba] or [da]) led to a decrease in the number of test stimuli identified as [ba], whereas adapting with the continuant sound [wa] led to an increase in the number of [ba] identification responses. Removing the vowel portion of an adapting stimulus greatly reduced the identification shift only when the resulting stimulus was no longer perceived as speech-like. A reduction in the number of [ba] identifications occurred even when a nonspeech “stop” (the sound of a plucked string) was used as the adapting stimulus, suggesting that phonetic processing is not a necessary condition for an adaptation effect.     

Configural biases and reversible figures: evidence of multilevel grouping effects

Four experiments sought to identify the processes underlying 2 classes of grouping effects that are readily produced with a hierarchical figure type known as ambiguous triangles. Previous work has shown that aligning small equilateral triangles in particular configurations can both facilitate and interfere with observers' ability to report the pointing direction of the individual triangles. We determined that selectively adapting the observer to low-frequency gratings of the same orientation as the aligned triangles markedly altered the interfering and facilitative effects of the global configuration only when an accuracy measure of performance was used. When a response latency measure was used, no effect of the same adaptation condition was found. Results are discussed in terms of multiple levels of grouping effects in the visual system and the differential sensitivity of these levels to basic neural adaptation.     

Effects of angularity of the figures with sharp and round corners on visual evoked potentials

Following a study in which equilateral triangles elicited larger visual evoked potentials (VEPs) than either squares or circles, we examined the effect of single-line angular figures with a sharp or a round corner at angles of 45°, 90°, 135° or 180°. VEPs were recorded monopolarly at four locations on the midline of scalp for 10 subjects, while the figure was tachiscopically presented to the lower visual field. Subtracted waves were obtained between figure and control (blank) conditions. N1 (peak latency 135–142 ms) and P2 (235–237 ms) waves were identifiable. N1 amplitude tended to decrease as a function of angularity, irrespective of orientation (angle pointing up or down). The effect of the sharpness/roundness of the corner was much smaller than that of its angularity. These findings suggest that the greater VEP response with triangles than with squares and circles may be attributable to the acute angularity of triangles. Related cortical processes and VEP components are also discussed.     

Metameric intransitivity

There are two kinds of afterimages. In negative afterimages, looking at a blank field after staring at a colored figure gives a figure whose color is complementary to that of the original figure. Less well understood and studied is the phenomenon of induced positive afterimages, in which staring at a colored area surrounding a small white test patch produces an afterimage in which the hue of the surround is transferred into the previously white area. Using these differences between positive and negative afterimages and also simultaneous color contrast, which has an effect on a test patch different from either of the afterimage effects, we describe a new effect, metameric intransitivity, in which perceptually similar images can generate markedly different afterimages, whereas perceptually different images can generate indistinguishable afterimages. Supplemental figures depicting the stimuli, results, and method for generating the intransitive metamers in this study may be downloaded from http://app.psychonomic-journals.org/content/supplemental.     

Response organization in selective adaptation to speech sounds

Previous experiments in speech perception using the selective adaptation procedure have found a shift in the locus of the category boundary for a series of speech stimuli following repeated exposure to an adapting syllable. The locus of the boundary moves toward the category of the adapting syllable. Most investigators have interpreted these findings in terms of feature detector models in which specific detectors are reduced in sensitivity through repeated adaptation. The present experiment was conducted to determine whether the adaptation results might be due to changes in response organization as a consequence of the labeling instructions presented to subjects in selective adaptation experiments. A perceptually ambiguous speech stimulus was selected from the middle of a [bi]-[di] test series and used as an adaptor under two different sets of instructions. One group of subjects was told that the adapting stimulus was the syllable [bi], while another group was told that the stimulus was the syllable [di]. The acoustically ambiguous adaptor failed to produce a shift in the locus of the category boundary in the direction predicted on the basis of the labeling instructions presented to subjects. These results indicate that the acoustic attributes and perceived quality of the adapting stimulus determine the direction and magnitude of the adaptation effects rather than the labels provided by the experimenter.     

“Extinction” of the McCollough effect does not transfer interocularly

A McCollough effect was induced in subjects by having them view typical adapting stimuli binocularly for 5 min. In the control condition, the strength of the McCollough effect was measured 20 min after the end of the adaptation. The strength was measured during monocular and binocular viewing of a test pattern via a color cancellation technique. Monocular strengths for the two eyes of a given subject were equal to each other and slightly weaker than the binocular strength. In the test condition, 15 min of the 20 min between adaptation and testing were spent monocularly viewing black and white gratings of the same orientation and spatial frequency as the adapting gratings. The strength of the effect as measured ipsilaterally was markedly decreased from that in the control condition. The strength of the effect as measured with the contralateral eye showed only a small decrease from that of the control condition. This finding is relevant to various models of the McCollough effect and related color aftereffects, especially those that posit a “learning” type of mechanism between achromatic spatial channels (which exhibit clear interocular transfer of various achromatic effects) and monocular color channels.     

Functional equivalence of masking and cue reduction in perception of shape at a slant

The present study was undertaken to investigate the effects of syllabic stress and segment structure on selective adaptation in speech. To this end, a CV place of articulation test continuum was selectively adapted by seven different adapting stimuli; the monosyllables [ba] and [ga], two disyllabic stimuli containing equal stress on both syllables, [baga] and [gabal, and three disyllabic stimuli ([baga]) in which stress placement varied and was cued by the acoustic parameters of fundamental frequency and duration. Results for the two adapting stimuli demonstrated significant [b] adaptation for the stimulus [ba] and significant [g] adaptation for [gal. Of the five other adapting stimuli, only [g] adaptation for the stimulus [bagá] was found to be significant. These findings indicate that the operation of detector mechanisms susceptible to fatigue by an adapting stimulus are even more constrained than has heretofore been suggested. It appears that the adapting and test stimuli must not only have the same phonetic and syllable structure, but also the same syllabic organization.     

The auditory motion aftereffect: its tuning and specificity in the spatial and frequency domains

In this paper, the auditory motion aftereffect (aMAE) was studied, using real moving sound as both the adapting and the test stimulus. The sound was generated by a loudspeaker mounted on a robot arm that was able to move quietly in three-dimensional space. A total of 7 subjects with normal hearing were tested in three experiments. The results from Experiment 1 showed a robust and reliable negative aMAE in all the subjects. After listening to a sound source moving repeatedly to the right, a stationary sound source was perceived to move to the left. The magnitude of the aMAE tended to increase with adapting velocity up to the highest velocity tested (20 degrees/sec). The aftereffect was largest when the adapting and the test stimuli had similar spatial location and frequency content. Offsetting the locations of the adapting and the test stimuli by 20 degrees reduced the size of the effect by about 50%. A similar decline occurred when the frequency of the adapting and the test stimuli differed by one octave. Our results suggest that the human auditory system possesses specialized mechanisms for detecting auditory motion in the spatial domain.     

The auditory motionaftereffect: Its tuning and specificity in the spatial and frequency domains

In this paper, the auditory motion aftereffect (aMAE) was studied, using real moving sound as both the adapting and the test stimulus. The sound was generated by a loudspeaker mounted on a robot arm that was able to move quietly in three-dimensional space. A total of 7 subjects with normal hearing were tested in three experiments. The results from Experiment 1 showed a robust and reliable negative aMAE in all the subjects. After listening to a sound source moving repeatedly to the right, a stationary sound source was perceived to move to the left. The magnitude of the aMAE tended to increase with adapting velocity up to the highest velocity tested (20°/sec). The aftereffect was largest when the adapting and the test stimuli had similar spatial location and frequency content. Offsetting the locations of the adapting and the test stimuli by 20° reduced the size of the effect by about 50%. A similar decline occurred when the frequency of the adapting and the test stimuli differed by one octave. Our results suggest that the human auditory system possesses specialized mechanisms for detecting auditory motion in the spatial domain.     

Cholinergic agents and the McCollough effect

The strength of the McCollough effect (ME), a pattern-contingent colour aftereffect, has been shown to be inversely related to acetylcholine, being significantly strengthened by (anticholinergic) scopolamine and weakened by (cholinergic) physostigmine delivered before adapting to the ME stimuli. The purpose of the present study was (i) to establish whether the effect of pre-adaptation scopolamine is linearly dose-dependent and (ii) to investigate the effects of scopolamine and physostigmine delivered between adaptation and testing. In experiment 1, ten healthy male volunteers who received placebo, or 0.6 mg, 1.2 mg, or 1.8 mg scopolamine before adapting to ME stimuli showed a significant linear dose-dependence over tests repeated from 10 to 70 min after adaptation. In experiment 2 twelve male volunteers adapted to ME stimuli and then received placebo, 1.2 mg oral scopolamine, or 0.75 mg subcutaneous physostigmine. On subsequent repeated testing, strength of the ME was increased by scopolamine and decreased by physostigmine relative to placebo. Both experiments were double-blind double-dummy repeated measures. These data support the view that the ME is a product of inhibitory mechanisms in the visual system rather than processes involved in associative learning.     

Contrast and frequency competition for orientation-contingent color aftereffects

A “competition” paradigm was developed to examine separately the effects of pattern contrast and spatial frequency characteristics on the strength of orientation-contingent color aftereffects (McCollough effects). After adapting to alternately presented red/black and green/black square-wave gratings (one horizontal, one vertical), 11 subjects viewed seven different kinds of test patterns. Unlike Standard McCollough effect test stimuli, the present patterns had variable luminance profiles running both horizontally and vertically within each test pattern area. Forced choice responses were used to determine which aftereffect color (red or green) appeared, as characteristics of vertical and horizontal luminance profiles were varied separately among test stimulus types. We conclude that pattern contrast and human contrast sensitivity account for aftereffect colors in such stimuli. When contrast is taken into consideration, aftereffects are not predicted by similarity between adaptation and test pattern Fourier characteristics, nor are they predicted by the width, per se, of pattern elements.     

The interplay between stereopsis and structure from motion

In a series of psychophysical experiments, an adaptation paradigm was employed to study the influence of stereopsis on perception of rotation in an ambiguous kinetic depth (KD) display. Without prior adaptation or stereopsis, a rotating globe undergoes spontaneous reversals in perceived direction of rotation, with successive durations of perceived rotation being random variables. Following 90 sec of viewing a stereoscopic globe undergoing unambiguous rotation, the KD globe appeared to rotate in a direction opposite that experienced during the stereoscopic adaptation period. This adaptation aftereffect was short-lived, and it occurred only when the adaptation and test figures stimulated the same retinal areas, and only when the adaptation and test figures rotated about the same axis. The aftereffect was just as strong when the test and adaptation figures had different shapes, as long as the adaptation figure contained multiple directions of motion imaged at different retinal disparities. Nonstereoscopic adaptation figures had no effect on the perceived direction of rotation of the ambiguous KD figure. These results imply that stereopsis and motion strongly interact in the specification of structure from motion, a result that complements earlier work on this problem.     

Evidence of rapid recovery from perceptual odor adaptation using a new stimulus paradigm

By attenuating neural and perceptual responses to sustained stimulation, adaptation enhances the detection of new, transient stimuli. Disadaptation serves a similarly important role as a temporal filter for chemoreceptor cells, producing rapid recovery of sensitivity upon termination of the adapting odorant. Previous research from our laboratory indicated that a rapid form of odor adaptation can be measured using a novel, simultaneous-odorant paradigm. In the present study, we extended the earlier method by measuring recovery from adaptation. Perceptual odor adaptation was measured by estimating psychophysical detection thresholds in a group of college-aged student volunteers (N = 20; 12 females, eight males) for a self-adapting odorant, vanilla extract. To induce adaptation, the time between the onset of the adapting odorant and the onset of the target odorant was systematically varied. By first quantifying adaptation, recovery of sensitivity could therefore be investigated by using different time points following the termination of the adapting odorant. Consistent with our previous work, thresholds estimated in the presence of the simultaneous adapting odorant were significantly increased, reflecting a decrease in sensitivity due to adaptation. Conversely, approximately 100 ms following termination of the adapting stimulus (the briefest delay tested), sensitivity began to rapidly recover. Nevertheless, some residual adaptation was evident at the longest offset delay of 500 ms. These findings suggest that the recovery from adaptation proceeds at least as rapidly as the onset of adaptation, a finding that is consistent with physiological evidence from olfactory receptors. These data also suggest the effectiveness of this new odorant paradigm in characterizing the temporal characteristics underlying these critical olfactory mechanisms.     

Adaptation to spiral motion in crowding condition

When a single, moving stimulus is presented in the peripheral visual field, its direction of motion can be easily distinguished, but when the same stimulus is flanked by other similar moving stimuli, observers are unable to report its direction of motion. In this condition, known as 'crowding', specific features of visual stimuli do not access conscious perception. The aim of this study was to investigate whether adaptation to spiral motion is preserved in crowding conditions. Logarithmic spirals were used as adapting stimuli. A rotating spiral stimulus (target spiral) was presented, flanked by spirals of the same type, and observers were adapted to its motion. The observers' task was to report the rotational direction of a directionally ambiguous motion (test stimulus) presented afterwards. The directionally ambiguous motion consisted of a pair of spirals flickering in counterphase, which were mirror images of the target spiral. Although observers were not aware of the rotational direction of the target and identified it at chance levels, the direction of rotation reported by the observers during the test phase (motion aftereffect) was contrarotational to the direction of the adapting spiral. Since all contours of the adapting and test stimuli were 90 degrees apart, local motion detectors tuned to the directions of the mirror-image spiral should fail to respond, and therefore not adapt to the adapting spiral. Thus, any motion aftereffect observed should be attributed to adaptation of global motion detectors (ie rotation detectors). Hence, activation of rotation-selective cells is not necessarily correlated with conscious perception.     

Acoustic feature analysis in the perception of voicing contrasts

Various types of acoustic cues have been shown to signal voicing contrasts in initial prestressed stop consonants. Two of the most important of these cues are the time interval between the release burst and the onset of voicing (voice onset time) and the duration of voiced transitions. In the present experiment, a selective adaptation procedure was used to investigate possible feature extraction mechanisms which underlie the perception of voicing. Subjects first identified either of two series of test stimuli, [ba-p^ha) or [ga-k^ha]. Next they listened to repeated presentations of an adapting stimulus and then again identified the original test series. Adapting stimuli having the same value of voice onset time but different voiced transition durations produced differential (and sometimes opposite) effects on the identification of the test stimuli. In every case, the adapting stimulus with the greater duration of voiced transitions led to larger reduction in voiced responses or to a smaller increase in voiceless responses. These results are incompatible with models of voicing perception based strictly on detectors for voice onset time. The results also suggest that the adaptation effect occurs at a point in the system prior to the actual phonetic decision.     

Primacy effect in orienting responses to auditory stimuli of tones and music.

This 25 factorial experiment investigated the primacy effect in the orienting response. The type of stimuli (tone or "music"), stimulus intensities (loud or soft), length of adaptation period (same, 5 or 30 sec; or different, 5 min.), interstimulus intervals (5 or 30 sec.), and sex were studied. College students, 32 males and 32 females were randomly assigned to each group. In the same condition, the tone (or music) was soft (or loud) for 5 sec. (or 30 sec.) in adaptation and was then changed alternately without interruption to loud, soft, etc. (or soft, loud, etc.) for 5 sec. (or 30 sec.). The different condition was identical except for the length of adaptation period in which the stimuli sounded continously for 5 min. Analyses of the GSR manifestation of the orienting responses indicated: (a) an over-all primacy effect with the auditory stimuli and (b) the primacy effect occurred in the 5-sec.-same but not in the 30-sec.-same condition as predicted.