The spatial and temporal conditions for perceiving velocity as constant

Perceived velocities during a brief period of exposure (< 1.2 s) were measured to examine how much time is necessary to perceive velocity as constant. Moving sinusoidal gratings were used as stimuli at relatively low velocities. At the beginning of each stimulus presentation, a moving pattern was perceived as stationary until a critical time had passed. After that, perceived velocity was positively correlated with moving distance, irrespective of physical velocity below a critical moving distance. Beyond the critical moving distance, velocity was perceived as constant. A simple model is presented to explain these results.     

Attentional capture by onsets and offsets

Three experiments were conducted to examine whether human infants would form a categorical representation for the spatial relation between. Experiment 1 showed that 6- and 7-month-olds familiarized with stimuli depicting a diamond in different locations between two reference bars subsequently preferred a stimulus displaying the diamond located outside the bars over a stimulus displaying the diamond located in a novel position between the bars. Experiments 2 and 3 revealed that this preference could not be attributed to a failure to discriminate the location changes of the diamond between the bars or an a priori preference. The overall pattern of results indicates that 6- and 7-month-olds had formed a categorical representation for between. The findings are discussed in terms of factors affecting development of categorical representations for spatial relation information.     

Pattern preferences at birth and their interaction with habituation-induced novelty preferences

Three experiments are described which relate to models of infant visual preferences, and to the ways in which preferences can be modified or created by habituation. In all experiments newborn babies were used as subjects. In Experiments equated 1 and 2 infants were presented with pairs of stimuli that were equated for contour density but which differed in spatial frequency components. The preferences obtained give support to Banks and Salapatek's (1981, Journal of Experimental Child Psychology, 31, 1-45) model of infant preferences which predicts that the maximally preferred stimulus will be that which contains high amplitude spatial frequency components falling within the age group's peak contrast sensitivity. In Experiment 3 an infant-controlled habituation procedure was used. The results obtained suggest that strong natural preferences based on the infants' peak contrast sensitivity cannot be changed by habituating infants either to the preferred or to the nonpreferred member of a stimulus pair. However, where no prior preference exists between two stimuli that are perceptually highly discriminable, very strong novelty preferences are found after habituating newborns to either stimulus. The results suggest that the contrast sensitivity model can be a powerful predictor of preferential looking in newborns, and in addition are further evidence that preferences based on experience can be found from birth.     

Sensitivity to auditory‐tactile colocation in early infancy

An ability to detect the common location of multisensory stimulation is essential for us to perceive a coherent environment, to represent the interface between the body and the external world, and to act on sensory information. Regarding the tactile environment “at hand”, we need to represent somatosensory stimuli impinging on the skin surface in the same spatial reference frame as distal stimuli, such as those transduced by vision and audition. Across two experiments we investigated whether 6‐ (n = 14; Experiment 1) and 4‐month‐old (n = 14; Experiment 2) infants were sensitive to the colocation of tactile and auditory signals delivered to the hands. We recorded infants’ visual preferences for spatially congruent and incongruent auditory‐tactile events delivered to their hands. At 6 months, infants looked longer toward incongruent stimuli, whilst at 4 months infants looked longer toward congruent stimuli. Thus, even from 4 months of age, infants are sensitive to the colocation of simultaneously presented auditory and tactile stimuli. We conclude that 4‐ and 6‐month‐old infants can represent auditory and tactile stimuli in a common spatial frame of reference. We explain the age‐wise shift in infants’ preferences from congruent to incongruent in terms of an increased preference for novel crossmodal spatial relations based on the accumulation of experience. A comparison of looking preferences across the congruent and incongruent conditions with a unisensory control condition indicates that the ability to perceive auditory‐tactile colocation is based on a crossmodal rather than a supramodal spatial code by 6 months of age at least.     

Spatial frequencies and the cerebral hemispheres: contrast sensitivity, visible persistence, and letter classification

The hypothesis that the two cerebral hemispheres are specialized for processing different visual spatial frequencies was investigated in three experiments. No differences between the left and right visual fields were found for: (1) contrast-sensitivity functions measured binocularly with vertical gratings ranging from 0.5 to 12 cycles per degree (cpd); (2) visible persistence durations for 1- and 10-cpd gratings measured with a stimulus alternation method; and (3) accuracy (d') and reaction times to correctly identify digitally filtered letters as targets (L or H) or nontargets (T or F). One significant difference, however, was found: In Experiment 3, a higher decision criterion (beta) was used when filtered letters were identified in the right visual field than when they were identified in the left. The letters were filtered with annular, 1-octave band-pass filters with center spatial frequencies of 1, 2, 4, 8, and 16 cpd. Combining four center frequencies with three letter sizes (0.5 degrees, 1 degree, and 2 degrees high) made some stimuli equivalent in distal spatial frequency (cycles per object) and some equivalent in proximal spatial frequency (cycles per degree). The effective stimulus in the third experiment seemed to be proximal spatial frequency (cycles per degree) not distal (cycles per object). We conclude that each cerebral hemisphere processes visual spatial frequency information with equal accuracy but that different decision rules are used.     

The perception of identity by 6 1/2-month-old infants.

In Study 1, sixteen 6 1/2-month-olds were habituated to a Reversible stimulus (an upright face that could be perceived as an entirely different upright face when it was rotated 180 degrees) and to a Nonreversible stimulus (a face that could be perceived as upright in only one orientation). Following habituation for each type of stimulus, test trials paired the habituated face with a novel stimulus (an inversion of the same face). For both Reversible and Nonreversible stimuli, the physical difference between the old and new test stimuli was the same (a 180 degrees rotation); however, infants devoted more visual attention to the 180 degrees rotation only when it was a Reversible face, suggesting that the identity change was detected. Experiment 2 ruled out the explanation that infants might have failed to dishabituate to the inversion of the Nonreversible stimulus because they could not remember it. Results are interpreted as evidence that 6 1/2-month-old infants are not limited to face recognition based on similarity in pattern arrangement alone, but are capable of processing faces at a representational level.     

Understanding the effects of moving visual stimuli on unilateral neglect following stroke

Moving visual stimuli have been shown to reduce unilateral neglect (ULN), however, the mechanisms underlying these effects remain poorly understood. This study compared lateralised and non-lateralised moving visual stimuli to investigate whether the spatial characteristics or general alerting properties of moving visual stimuli are responsible for reducing neglect. Post-stroke left neglect patients as well as healthy and patient control subjects were tested on a computerised line bisection task under six visual stimulus conditions. The key finding was that, relative to the no stimulus condition, leftward moving and left-sided moving visual stimuli shifted neglect patients' bisection errors leftward while the non-lateralised random moving visual stimuli did not reduce neglect patients' rightward bisection errors. The results provide evidence that spatial characteristics rather than general alerting properties of moving visual stimuli reduce rightward bisection errors in ULN. Moreover, the pattern of findings strongly supports the notion that moving visual stimuli reduce neglect by capturing attention and drawing it to a spatial location rather than by activating the attentional system via superior collicular neurons.     

Interpreting the effects of image manipulation on picture perception in pigeons (Columba livia) and humans (Homo sapiens)

The effects of picture manipulations on humans' and pigeons' performance were examined in a go/no-go discrimination of two perceptually similar categories, cat and dog faces. Four types of manipulation were used to modify the images. Mosaicization and scrambling were used to produce degraded versions of the training stimuli, while morphing and cell exchange were used to manipulate the relative contribution of positive and negative training stimuli to test stimuli. Mosaicization mainly removes information at high spatial frequencies, whereas scrambling removes information at low spatial frequencies to a greater degree. Morphing leads to complex transformations of the stimuli that are not concentrated at any particular spatial frequency band. Cell exchange preserves high spatial frequency details, but sometimes moves them into the "wrong" stimulus. The four manipulations also introduce high-frequency noise to differing degrees. Responses to test stimuli indicated that high and low spatial frequency information were both sufficient but not necessary to maintain discrimination performance in both species, but there were also species differences in relative sensitivity to higher and lower spatial frequency information.     

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.     

Changes in infants' visual scanning across the 2- to 14-week age period

The characteristics of visual scanning over the 2- to 14-week age period were examined through repeated assessments conducted on a sample of 10 infants. Scanning patterns were measured using a bright-pupil corneal reflex system, and the stimuli consisted of various sets of static, moving, or flickering geometric figures. There appear to be a number of age-related changes in the dominant mode of visual scanning. At the youngest ages the infants' scanning often proved unrelated to the locations of the stimulus contours, and in instances where a stimulus figure was in fact attended the infants typically centered their regard on a single prominent feature. In contrast, as the infants grew older they more consistently directed their saccades toward stimulus contours, became increasingly disposed to scan between different stimulus features, and directed their saccades with increased accuracy. When a stimulus was flickering, however, the infants' scanning characteristics reverted to those typically found at younger ages. The mechanisms which might account for the effects of age and of stimulus quality on visual scanning are considered.     

Adaptation to auditory motion in the horizontal plane: effect of prior exposure to motion on motion detectability.

Thresholds for auditory motion detectability were measured in a darkened anechoic chamber while subjects were adapted to horizontally moving sound sources of various velocities. All stimuli were 500-Hz lowpass noises presented at a level of 55 dBA. The threshold measure employed was the minimum audible movement angle (MAMA)--that is, the minimum angle a horizontally moving sound must traverse to be just discriminable from a stationary sound. In an adaptive, two-interval forced-choice procedure, trials occurred every 2-5 sec (Experiment 1) or every 10-12 sec (Experiment 2). Intertrial time was "filled" with exposure to the adaptor--a stimulus that repeatedly traversed the subject's front hemifield at ear level (distance: 1.7 m) at a constant velocity (-150 degrees/sec to +150 degrees/sec) during a run. Average MAMAs in the control condition, in which the adaptor was stationary (0 degrees/sec,) were 2.4 degrees (Experiment 1) and 3.0 degrees (Experiment 2). Three out of 4 subjects in each experiment showed significantly elevated MAMAs (by up to 60%), with some adaptors relative to the control condition. However, there were large intersubject differences in the shape of the MAMA versus adaptor velocity functions. This loss of sensitivity to motion that most subjects show after exposure to moving signals is probably one component underlying the auditory motion aftereffect (Grantham, 1989), in which judgments of the direction of moving sounds are biased in the direction opposite to that of a previously presented adaptor.     

Fourier components of moving gratings

In designing experiments in which the proximal stimulus is a moving grating (including cases in which the distal stimulus is stationary but eye movements play a significant role), one must consider the effects of the motion of the stimulus on its Fourier components in the spatiotemporal frequency domain. Some of these effects are unexpected and counterintuitive. For example, the Fourier components of a moving grating do not include its stationary (or “instantaneous”) spatial frequency. Thus there is no linear filter that can extract a stationary grating from a moving one. Several useful relations are given for analyzing such stimuli.     

Intermodal perception at birth: Intersensory redundancy guides newborn infants’ learning of arbitrary auditory−visual pairings

In this study the ability of newborn infants to learn arbitrary auditory–visual associations in the absence versus presence of amodal (redundant) and contingent information was investigated. In the auditory-noncontingent condition 2-day-old infants were familiarized to two alternating visual stimuli (differing in colour and orientation), each accompanied by its ‘own’ sound: when the visual stimulus was presented the sound was continuously presented, independently of whether the infant looked at the visual stimulus. In the auditory-contingent condition the auditory stimulus was presented only when the infant looked at the visual stimulus: thus, presentation of the sound was contingent upon infant looking. On the post-familiarization test trials attention recovered strongly to a novel auditory–visual combination in the auditory-contingent condition, but remained low, and indistinguishable from attention to the familiar combination, in the auditory-noncontingent condition. These findings are a clear demonstration that newborn infants’ learning of arbitrary auditory–visual associations is constrained and guided by the presence of redundant (amodal) contingent information. The findings give strong support to Bahrick’s theory of early intermodal perception.     

The development of contrast constancy

The mature visual system possesses mechanisms that enable invariant perception of the contrast of an object and its features as the object undergoes changes in distance. This phenomenon, which has been called contrast constancy, obtains at suprathreshold contrasts only. Some models of contrast constancy assume the presence of narrowband spatial-frequency channels. An implication of M.S. Banks, B.R. Stephens, and E.E. Hartmann (1985, Journal of Experimental Child Psychology, 40, 501-527) is that contrast constancy should not be observed at 6 weeks but may be observed at 12 weeks. We examined this implication by investigating the development of contrast constancy in 6- and 12-week-old infants. Two sine wave gratings, differing in spatial frequency by a factor of 3, were presented side-by-side. The contrast of one grating was varied in order to estimate the contrast at which preference for the two gratings was equal. The equal preference points for 6-week-olds were predictable from their contrast thresholds. The 12-week-olds' equal preference points for low-contrast stimuli were predictable from their contrast thresholds, but those for intermediate and high-contrast stimuli were not. Thus, if one accepts the assumption that equal preference in infants is analogous to apparent contrast matches in adults, these data imply that contrast constancy is observed at 12 weeks but not 6 weeks. The perceptual consequences of this developmental transition are discussed.     

The effect of spatial-frequency filtering on the visual processing of global structure

In three experiments we measured reaction times (RTs) and error rates in identifying the global structure of spatially filtered stimuli whose spatial-frequency content was selected by means of three types of 2-D isotropic filters (Butterworth of order 2, Butterworth of order 10, and a filters with total or partial Gaussian spectral profile). In each experiment, low-pass (LP), bandpass (BP), and high-pass (HP) filtered stimuli, with nine centre or cut-off spatial frequencies, were used. Irrespective of the type of filter, the experimental results showed that: (a) RTs to stimuli with low spatial frequencies were shorter than those to stimuli with medium or high spatial frequencies, (b) RTs to LP filtered stimuli were nearly constant, but they increased in a nonmonotonic way with the filter centre spatial frequency in BP filtered stimuli and with the filter cut-off frequency in HP filtered stimuli, and (c) the identification of the global pattern occurred with all visible stimuli used, including BP and HP images without low spatial frequencies. To remove the possible influence of the energy, a fourth experiment was conducted with Gaussian filtered stimuli of equal contrast power (c(rms) = 0.065). Similar results to those described above were found for stimuli with spatial-frequency content higher than 2 cycles deg(-1). A model of isotropic first-order visual channels collecting the stimulus spectral energy in all orientations explains the RT data. A subsequent second-order nonlinear amplitude demodulation process, applied to the output of the most energetic first-order channel, could explain the perception of global structure of each spatially filtered stimulus, including images lacking low spatial frequencies.     

The effect of central and peripheral field stimulation on the rise time and gain of human optokinetic nystagmus

We wished to examine the spatial (gain) and temporal (rise time) properties of human optokinetic nystagmus (OKN) as a function of stimulus velocity and field location. Stimuli were either M-scaled random dots or vertical stripes that moved at velocities between 20-80 deg s(-1). Three field conditions were examined: full field; a 20 deg central field; and a 12.5 deg central-field mask. OKN gain was found to be significantly affected by stimulus velocity and stimulus location, with the higher stimulus velocities and the 12.5 deg central-field mask giving lower gains. Steady-state gains for all three field conditions were not found to be affected by prior adaptation to stationary or moving stimuli. The 63% rise time was found to be significantly affected by the stimulus velocity, whereas this was not the case for the 90% rise time. Neither rise time was found to be significantly affected by the field location. These results indicate that, although the effectiveness (gain) of peripheral retina is lower than that of the central retina during optokinetic stimulation, the peripheral retina has access to common mechanisms responsible for the fast component of OKN.     

Chicks prefer to peck at insect-like elongated stimuli moving in a direction orthogonal to their longer axis

Spontaneous preferences towards possible prey have been little investigated using targets in motion. Preferences of domestic chicks (Gallus gallus) to peck at video-images of stimuli representing live insects moving along their longer body axis (i.e. “forwards”) or along the shorter body axis (i.e. “sideways”) were investigated. Chicks presented with both types of stimulus displayed a significant preference for pecking at stimuli moving sideways. This preference was already present on day 1 post-hatching, and it strengthened on day 6 for those chicks that had experienced pecking at live insects. Head angles used to fixate the stimuli prior to pecking were also analysed and were consistent (i.e. 30°–35° and 60°–65°) with those reported for fixation of non-edible targets (larger stimuli at a distance). In a first control experiment the same video-presented stimuli were used but the insect’s legs were removed to reduce flickering. In a second control experiment, paper-printed images of the whole insect were used. In both cases, the sideways direction of movement was clearly preferred. Overall, our data show that chicks have a spontaneous preference to peck at video-images resembling live insects moving along their shorter body axis. Sideways movement may constitute a crucial signal attracting chicks’ attention and enhancing predatory responses possibly because of stronger stimulation of motion detectors.     

A comparison of visual and auditory representational momentum in spatial tasks

Similarities have been observed in the localization of the final position of moving visual and moving auditory stimuli: Perceived endpoints that are judged to be farther in the direction of motion in both modalities likely reflect extrapolation of the trajectory, mediated by predictive mechanisms at higher cognitive levels. However, actual comparisons of the magnitudes of displacement between visual tasks and auditory tasks using the same experimental setup are rare. As such, the purpose of the present free-field study was to investigate the influences of the spatial location of motion offset, stimulus velocity, and motion direction on the localization of the final positions of moving auditory stimuli (Experiment 1 and 2) and moving visual stimuli (Experiment 3). To assess whether auditory performance is affected by dynamically changing binaural cues that are used for the localization of moving auditory stimuli (interaural time differences for low-frequency sounds and interaural intensity differences for high-frequency sounds), two distinct noise bands were employed in Experiments 1 and 2. In all three experiments, less precise encoding of spatial coordinates in paralateral space resulted in larger forward displacements, but this effect was drowned out by the underestimation of target eccentricity in the extreme periphery. Furthermore, our results revealed clear differences between visual and auditory tasks. Displacements in the visual task were dependent on velocity and the spatial location of the final position, but an additional influence of motion direction was observed in the auditory tasks. Together, these findings indicate that the modality-specific processing of motion parameters affects the extrapolation of the trajectory.     

Perceived path of oblique motion: horizontal-vertical and stimulus-orientation effects

Subjects adjusted the path of moving stimuli to produce apparent slopes of 45 degrees with respect to horizontal. The stimulus was either a single moving dot or a vertical or horizontal bar. In separate experiments either the stimuli were tracked or fixation was maintained on a stationary fixation target positioned 8 deg to the right of the center of stimulus motion. In both experiments the selected path slopes were in general more horizontal than 45 degrees. This pattern indicates that subjects overestimate the vertical component of motion along an oblique path, and is interpreted as a manifestation of the spatial anisometropy generally termed the 'horizontal-vertical illusion'. Additionally, paths selected for horizontal bars were more vertical than those for vertical bars. This finding is interpreted in the context of a previous report of the influence of stimulus orientation on perceived velocity.     

The detection of slow stimulus movement in 2- to 5-month-olds

Preferences for moving over static bars were assessed in 8-, 16-, and 20-week-old human infants. The display consisted of two adjacent horizontal bars one of which moved with one of four velocities (0.70, 1.4, 2.8 or 5.6 degrees/s) through one of four distances (11, 22, 44, or 88 arcmin) before reversing and traveling in the other direction at the same velocity. No significant preferences for motion were obtained at 8 weeks. At both 16 and 20 weeks of age, however, preferences for motion were determined exclusively by the velocity of the movement and were unaffected by the excursion of the bar. The minimum velocities that elicited significant preferences for motion were 5.08 degrees/s and 2.32 degrees/s at 16 and 20 weeks of age, respectively. The more attentive 20-week-olds, however, showed significant preferences for motion above a velocity of approximately 1.8 degrees/s. The addition of static reference bars had little influence on these preferences for motion in 20-week-olds; preferences were again related exclusively to the velocity of the bar's movement. The results are discussed in terms of the development of motion-sensitive mechanisms within the visual system.