“Parts” of perceived visual forms: New evidence

The Pulfrich effect (the illusory displacement of a moving stimulus when it is viewed with an optical filter over one eye) was measured repeatedly during a 20 min period following the initial filtering of the eye. For each of 10 filter densities, the Pulfrich effect always occurred immediately upon filtering the eye, but subsequently increased greatly during the adaptation period. The results indicate that the perceptual latency of the filtered eye is increased by two factors: the reduction in stimulus luminance due to the filter and progressive dark adaptation. Dark adaptation is apparently the more important of these two factors.     

Perceptual masking: Peripheral vs central factors

Perceptual masking was studied under binocular and dichoptic conditions in order to separate peripheral and central interference effects. Under binocular conditions, when the test flash (TF) and the blanking flash (BF) fell on both retinas, both retroactive and proactive masking were demonstrated. Under dichoptic conditions, when the TF fell on one eye and the BF on the other eye, thus eliminating opportunity for intraretinal interference, there was partial retroactive perceptual masking and no proactive masking. These results suggest that binocular proactive masking is due to peripheral light adaptation, that binocular retroactive masking is due to both peripheral and central effects, and that dichoptic masking is due solely to central retrochiasmal interference. It is proposed that dichoptic retroactive perceptual masking affords a method of investigating central perception time, i.e., the time to consolidate a perceptual experience.     

Instrumentation designed to simulate the effects of prisms used in studies of visual rearrangement

A system is described which simulates some of the visual rearrangements and changes in sensorimotor relations that occur when experimental subjects move their eyes while looking through a contact lens with a prism attached. The simulated system is more convenient than a system based on the use of a contact lens, and it is based on measures of eye movement that are important in research on the perceptual effects of visual rearrangement. The effects that occur are reviewed in this paper. We also show in detail how the artificial system, which has an eye movement monitor interfaced with a computer and display, simulates the former effects. The data show that experimental subjects who experience visual rearrangement by simulated means manifest the same kind of perceptual adaptation produced in studies in which visual rearrangement is generated by means of a prism mounted on a contact lens.     

Tracking without perceiving: a dissociation between eye movements and motion perception

Can people react to objects in their visual field that they do not consciously perceive? We investigated how visual perception and motor action respond to moving objects whose visibility is reduced, and we found a dissociation between motion processing for perception and for action. We compared motion perception and eye movements evoked by two orthogonally drifting gratings, each presented separately to a different eye. The strength of each monocular grating was manipulated by inducing adaptation to one grating prior to the presentation of both gratings. Reflexive eye movements tracked the vector average of both gratings (pattern motion) even though perceptual responses followed one motion direction exclusively (component motion). Observers almost never perceived pattern motion. This dissociation implies the existence of visual-motion signals that guide eye movements in the absence of a corresponding conscious percept.     

Light and dark adaptation of visually perceived eye level controlled by visual pitch

The pitch of a visual field systematically influences the elevation at which a monocularly viewing subject sets a target so as to appear at visually perceived eye level (VPEL). The deviation of the setting from true eye level averages approximately 0.6 times the angle of pitch while viewing a fully illuminated complexly structured visual field and is only slightly less with one or two pitched-from-vertical lines in a dark field (Matin & Li, 1994a). The deviation of VPEL from baseline following 20 min of dark adaptation reaches its full value less than 1 min after the onset of illumination of the pitched visual field and decays exponentially in darkness following 5 min of exposure to visual pitch, either 30° topbackward or 20° topforward. The magnitude of the VPEL deviation measured with the dark-adapted right eye following left-eye exposure to pitch was 85% of the deviation that followed pitch exposure of the right eye itself. Time constants for VPEL decay to the dark baseline were the same for same-eye and cross-adaptation conditions and averaged about 4 min. The time constants for decay during dark adaptation were somewhat smaller, and the change during dark adaptation extended over a 16% smaller range following the viewing of the dim two-line pitched-from-vertical stimulus than following the viewing of the complex field. The temporal course of light and dark adaptation of VPEL is virtually identical to the course of light and dark adaptation of the scotopic luminance threshold following exposure to the same luminance. We suggest that, following rod stimulation along particular retinal orientations by portions of the pitched visual field, the storage of the adaptation process resides in the retinogeniculate system and is manifested in the focal system as a change in luminance threshold and in the ambient system as a change in VPEL. The linear model previously developed to account for VPEL, which was based on the interaction of influences from the pitched visual field and extraretinal influences from the body-referenced mechanism, was employed to incorporate the effects of adaptation. Connections between VPEL adaptation and other cases of perceptual adaptation of visual direction are described.     

Concomitant direction and distance aftereffects of sustained convergence: A muscle potentiation explanation for eye-specific adaptation

Fixating a target for 6 min was shown to produce distance aftereffects that varied in direction and magnitude as a linear function of the convergence angle. Eye-specific direction aftereffects also were obtained in a nasal direction under conditions that produce increased perceived distance and in a temporal direction under conditions that produce decreased perceived distance. These aftereffects were shown to be sensitive to the range of horizontal versional eye movements that accompany the near or far convergence positions maintained during exposure. The results provide a logical alternative to perceptual learning accounts of eye-specific adaptation.     

Effects of load on the time course of attentional engagement,disengagement, and orienting in reading

Sensory-motor delays vary over the course of development and under different environmental conditions. Previous research has shown that humans can compensate for the resulting temporal misalignment while performing sensory-motor tasks (e.g., Cunningham, Billock, & Tsou, 2001a), but remains silent on the question of whether perceptual learning—similar to that involved in adaptation to spatial misalignment (e.g., Redding & Wallace, 1993) and in adaptation to purely intersensory misalignment (e.g., Fujisaki, Shimojo, Kashino, & Nishida, 2004)—is also involved in this adaptive response. Following an attempted replication of Cunningham et al.'s (2001a) study in a preliminary experiment, we present in this paper two experiments that demonstrate that after-effects of adaptation to temporal misalignment do not spontaneously decay. The literature on adaptation to spatial misalignment suggests that, while instrumental learning spontaneously decays in the absence of reinforcement, perceptual learning persists. Therefore our results are consistent with adaptation being effected through perceptual learning.     

Adaptation to sensory-motor temporal misalignment: instrumental or perceptual learning?

Sensory-motor delays vary over the course of development and under different environmental conditions. Previous research has shown that humans can compensate for the resulting temporal misalignment while performing sensory-motor tasks (e.g., Cunningham, Billock, & Tsou, 2001a), but remains silent on the question of whether perceptual learning-similar to that involved in adaptation to spatial misalignment (e.g., Redding & Wallace, 1993) and in adaptation to purely intersensory misalignment (e.g., Fujisaki, Shimojo, Kashino, & Nishida, 2004)-is also involved in this adaptive response. Following an attempted replication of Cunningham et al.'s (2001a) study in a preliminary experiment, we present in this paper two experiments that demonstrate that after-effects of adaptation to temporal misalignment do not spontaneously decay. The literature on adaptation to spatial misalignment suggests that, while instrumental learning spontaneously decays in the absence of reinforcement, perceptual learning persists. Therefore our results are consistent with adaptation being effected through perceptual learning.     

汉语双字词句知觉广度的眼动研究

阅读知觉广度通常指阅读者在阅读文本过程中每次注视能获取有用视觉信息的范围。既往的汉语知觉广度的研究一般把单字作为基本的知觉呈现单元,但在某些呈现条件下,此类呈现方式会导致阅读过程中的语义加工的完整性被破坏。本研究采用眼动追踪技术,使用移动窗口范式和中央凹掩蔽范式,使用双字词句作为阅读材料,双字词作为基本的知觉呈现单元,探讨在保证知觉呈现单元语义完整性的基础上大学生的汉语阅读知觉广度。实验一采用移动窗口范式,结果发现,知觉广度范围为注视词左侧1个双字词及右侧1-2个双字词的空间。实验二采用中央凹掩蔽范式,结果验证了实验一的研究结果。该结果表明,在汉语阅读过程中,以双字词为基本的视觉呈现单元,较既往研究中单字为基本呈现单元的情况,更好地保证了阅读中语义的完整性,从而获得了更大的知觉范围。该结果建立于视觉呈现单元的语义完整性的基础上,是对现有的汉语阅读知觉广度理论的完善和扩展。     

On the locus of the semantic satiation effect: Evidence from event-related brain potentials

The present study sought to determine whether semantic satiation is merely a by-product of adaptation or satiation of upstream, nonsemantic perceptual processes or whether the effect can have a locus in semantic memory. This was done by measuring event-related brain potentials (ERPs) in a semantic word-detection task involving multiple presentations of primes and critical related and unrelated words in three experiments involving visual (Experiment 1) and auditory (Experiments 2A and 2B) stimuli. Primes varied in their type case (Experiment 1) or pitch (Experiment 2B) in order to discourage sensory adaptation. Prime satiation and relatedness of the primes to the critical word had interacting effects on ERP amplitude to critical words, particularly within the time-window of the N400 component. Because numerous studies have indicated a role for the N400 in semantic processing, modulation of the N400 relatedness effect by prime satiation (with little or no contribution from perceptual adaptation) suggests that semantic memory can be directly satiated, rather than the cost to semantic processing necessarily resulting from impoverishment of perceptual inputs.     

Attention during adaptation weakens negative afterimages of perceptually colour-spread surfaces

The visual system can complete coloured surfaces from stimulus fragments, inducing the subjective perception of a colour-spread figure. Negative afterimages of these induced colours were first reported by S. Shimojo, Y. Kamitani, and S. Nishida (2001). Two experiments were conducted to examine the effect of attention on the duration of these afterimages. The results showed that shifting attention to the colour-spread figure during the adaptation phase weakened the subsequent afterimage. On the basis of previous findings that the duration of these afterimages is correlated with the strength of perceptual filling-in (grouping) among local inducers during the adaptation phase, it is proposed that attention weakens perceptual filling-in during the adaptation phase and thereby prevents the stimulus from being segmented into an illusory figure.     

Parafoveal Magnification: Visual Acuity Does Not Modulate the Perceptual Span in Reading

ABSTRACT— Models of eye guidance in reading rely on the concept of the perceptual span—the amount of information perceived during a single eye fixation, which is considered to be a consequence of visual and attentional constraints. To directly investigate attentional mechanisms underlying the perceptual span, we implemented a new reading paradigm—parafoveal magnification (PM)—that compensates for how visual acuity drops off as a function of retinal eccentricity. On each fixation and in real time, parafoveal text is magnified to equalize its perceptual impact with that of concurrent foveal text. Experiment 1 demonstrated that PM does not increase the amount of text that is processed, supporting an attentional-based account of eye movements in reading. Experiment 2 explored a contentious issue that differentiates competing models of eye movement control and showed that, even when parafoveal information is enlarged, visual attention in reading is allocated in a serial fashion from word to word.     

自然阅读与校对阅读的知觉广度研究

采用经典的移动窗口技术,以Eyelink2000型眼动仪为工具,探讨了自然阅读和校对阅读两种不同的任务对中文阅读知觉广度的影响,结果表明：（1）与校对阅读条件相比,自然阅读条件下的阅读速度更快、眼跳幅度更大。（2）自然阅读条件下被试的知觉广度为注视点右侧2-3个字;校对阅读条件下被试的知觉广度仅为注视点1个字的空间。结果说明,读者在校对阅读和自然阅读条件下采用了不同的阅读策略,阅读知觉广度的大小受任务要求的影响。     

Perceptual adaptation to facial asymmetries

Humans and other animals are highly sensitive to deviations from bilateral symmetry and prefer symmetric mates. Fluctuating asymmetries (FAs) are random deviations from perfect symmetry that can result from developmental instability. Human perceptions of facial asymmetry are driven by FAs and insensitive to directional asymmetries (DAs), which have a consistent direction of bias (e.g., left side always larger) across the population and are unrelated to developmental stability. We hypothesized that perceptual adaptation may filter out DAs and provide a proximate mechanism for this perceptual focus on FAs. We created a small population of faces with DAs by applying a unilateral distortion to the same side of each face. After 5 min of adaptation, (new) faces with these DAs looked less asymmetric and the most symmetric-looking distortion shifted toward the adapting asymmetry level. Parallel changes occurred for attractiveness. We suggest that perceptual adaptation may provide the proximate mechanism for an evolutionarily adaptive focus on FAs.     

Perceptual fading without retinal adaptation

A retinally stabilized object readily undergoes perceptual fading and disappears from consciousness. This startling phenomenon is commonly believed to arise from local bottom-up sensory adaptation to edge information that occurs early in the visual pathway, such as in the lateral geniculate nucleus of the thalamus or retinal ganglion cells. Here we use random dot stereograms to generate perceivable contours or shapes that are not present on the retina and ask whether perceptual fading occurs for such "cortical" contours. Our results show that perceptual fading occurs for "cortical" contours and that the time a contour requires to fade increases as a function of its size, suggesting that retinal adaptation is not necessary for the phenomenon and that perceptual fading may be based in the cortex.     

On counteradaptation

Often adaptation to artificially altered stimulation takes place because veridical stimulation that produces the same perceptual property that is produced by the altered stimulation is also received. In these cases, an assimilation of the two perceptual processes produced by the two different stimulations (the altered and the veridical) is supposed to be responsible for the adaptation that is achieved. This hypothesis, which was formulated by Wallach and Karsh (1963), would be confirmed by demonstrating a modification of the perceptual process produced by veridical stimulation rather than the one produced by the altered stimulation. We demonstrated this by having S observe in the dark for 20 min a luminous figure that objectively expanded as it moved toward S and contracted as it moved away. But instead of testing for changes in size perception as such, we tested for a change in the relation between accommodation and convergence on the one hand and registered distance on the other. In one experiment, such a change was measured by obtaining estimates of perceived size and depth before and after the adaptation period. Highly significant changes of size and significantly greater changes of stereoscopic depth were obtained. Inasmuch as stereoscopic vision was totally absent from the adaptation conditions, the change in stereoscopic depth that was larger than the size change can only be ascribed to a change in registered distance. In another experiment, we tested for a change in distance by having S point from the side to a vertical line, before and again after the adaptation period, under conditions where only accommodation and convergence could serve as distance cues. Significant changes in the pointing distance were measured, indicating more directly a change in the relation between these oculomotor adjustments and perceived distance. We propose the term counteradaptation for such modification of a perceptual process away from veridicality.     

Two kinds of adaptation in the constancy of visual direction and their different effects on the perception of shape and visual direction

Adaptation in the constancy of visual direction can be obtained under two radically different conditions, called eye-movement adaptation and field adaptation. Adaptation resulting from these conditions and from a “normal” condition was measured with a newly developed estimation test. Eye-movement adaptation was found to cause an alteration of compensatory eye movements. It apparently consists of a changed evaluation of eye movements, as demonstrated by two different pointing tests. A form test where the shape of a large oblong is set to look square also confirmed this interpretation. After field adaptation, a pointing test did not register a change, but an adaptation effect could be measured with a forward direction test. This test and a square test where no eye movements were permitted proved to be specific to field adaptation; they measured no effect after eye-movementadaptation. The normal adaptation condition Was apparently equivalent to the eye-movement adaptation condition. Its effect could be measured only with a pointing test. When we changed the normal adaptation condition so that frequent saccades were made during head turning, strong effects were measured with the two tests that were specific to field adaptation.     

Absence of binocular interaction between spatial and color attributes of visual stimuli

The hypothesis that induction of the McCollough effect (spatially selective color aftereffects) entails adaptation of monocularly driven detectors tuned to both spatial and color attributes of the visual stimulus was examined in four experiments. The McCollough effect could not be generated by displaying contour information to one eye and color information to the other eye during inspection, even in the absence of binocular rivalry. Nor was it possible to induce depth-specific color aftereffects following an inspection period during which random-dot stereograms were viewed, with crossed and uncrossed disparity seen in different colored light. Masking and aftereffect in the perception of stereoscopic depth were also nonselective to color; in both cases, perceptual distortion was controlled by stereospatial variables but not by the color relationship between the inspection and test stimuli. The results suggest that binocularly driven spatial detectors in human vision are insensitive to wavelength.     

Perceptual alternation induced by visual transients

When our visual system is confronted with ambiguous stimuli, the perceptual interpretation spontaneously alternates between the competing incompatible interpretations. The timing of such perceptual alternations is highly stochastic and the underlying neural mechanisms are poorly understood. We show that perceptual alternations can be triggered by a transient stimulus presented nearby. The induction was tested for four types of bistable stimuli: structure-from-motion, binocular rivalry, Necker cube, and ambiguous apparent motion. While underlying mechanisms may vary among them, a transient flash induced time-locked perceptual alternations in all cases. The effect showed a dependence on the adaptation to the dominant percept prior to the presentation of a flash. These perceptual alternations show many similarities to perceptual disappearances induced by transient stimuli (Kanai and Kamitani, 2003 Journal of Cognitive Neuroscience 15 664-672; Moradi and Shimojo, 2004 Vision Research 44 449-460). Mechanisms linking these two transient-induced phenomena are discussed.     

Using ambiguous plaid stimuli to investigate the influence of immediate prior experience on perception

In a series of three experiments, we used an ambiguous plaid motion stimulus to explore the behavioral and electrophysiological effects of prior stimulus exposures and perceptual states on current awareness. The results showed that prior exposure to a stimulus biased toward one percept led to subsequent suppression of that percept. In contrast, in the absence of stimulus bias, prior perceptual experience can have a facilitative influence. The suppressive effects caused by the prior stimulus were found to transfer to an ambiguous plaid test stimulus rotated 180º relative to the adaptation stimulus, but were abolished if (1) the ambiguous test stimulus was only rotated 90º relative to the adaptation stimulus or (2) the adaptation stimulus was heavily biased toward the component grating percept. Event-related potential recordings were consistent with the involvement of visual cortical areas and suggested that the influence of recent stimulus exposure may involve recruitment of additional brain processes beyond those responsible for initial stimulus encoding. In contrast, the effects of prior and current perceptual experience appeared to depend on similar brain processes. Although the data presented here focus on vision, the work is discussed within the context of data from a parallel series of experiments in audition.