Visual Search Remains Efficient When Visual Working Memory is Full

Many theories of attention have proposed that visual working memory plays an important role in visual search tasks. The present study examined the involvement of visual working memory in search using a dual-task paradigm in which participants performed a visual search task while maintaining no, two, or four objects in visual working memory. The presence of a working memory load added a constant delay to the visual search reaction times, irrespective of the number of items in the visual search array. That is, there was no change in the slope of the function relating reaction time to the number of items in the search array, indicating that the search process itself was not slowed by the memory load. Moreover, the search task did not substantially impair the maintenance of information in visual working memory. These results suggest that visual search requires minimal visual working memory resources, a conclusion that is inconsistent with theories that propose a close link between attention and working memory.     

视觉意识及其神经机制

视觉意识的神经机制是当前认知神经科学研究的热点问题之一。过去普遍认为视觉信息加工主要有两条通路:腹侧通路和背侧通路;而新近的研究表明还存在不经过初级视觉皮层(V1区)的第三条通路。高级视觉皮层、V1区和皮层下结构都对意识觉知的产生起到了相应的作用。已有的实验证据表明,意识的产生过程异常复杂,仍有很多问题值得继续深入讨论和研究。     

Visual memory as measured by classification and comparison tasks

One measure often used to indicate the existence of visual memory is visual priming, that is, faster responding to a stimulus physically identical to its predecessor than to one identical in name only. Walker and Marshall (1982) used visual priming within speeded classification tasks to demonstrate a visual memory effect that does not seem to require active visualization to prevent decay or to prevent being over-written by succeeding stimuli. This article presents six experiments with classification tasks that not only replicate Walker and Marshall's finding of a strong visual memory in the absence of visualization but also--contrary to their results--show visual priming even after an unpredictable intervening visual pattern. Four additional experiments with comparison tasks show visual priming effects only when stimulus-response contingencies remain consistent. Although this result seems to favor an explanation of the visual priming effect based on stimulus-response contingencies, it does not totally rule out explanations based on stimulus-identification processes, assuming that inconsistent stimulus-response contingencies interfere with the benefits that stimulus repetition may have on stimulus identification.     

Visuospatial tasks suppress craving for cigarettes

The Elaborated Intrusion (EI) theory of desire posits that visual imagery plays a key role in craving. We report a series of experiments testing this hypothesis in a drug addiction context. Experiment 1 showed that a mental visual imagery task with neutral content reduced cigarette craving in abstaining smokers, but that an equivalent auditory task did not. The effect of visual imagery was replicated in Experiment 2, which also showed comparable effects of non-imagery visual working memory interference. Experiment 3 showed that the benefit of visual over auditory interference was not dependent upon imagery being used to induce craving. Experiment 4 compared a visuomotor task, making shapes from modeling clay, with a verbal task (counting back from 100), and again showed a benefit of the visual over the non-visual task.We conclude that visual imagery supports craving for cigarettes. Competing imagery or visual working memory tasks may help tackle craving in smokers trying to quit.     

Effects of concurrent verbal memory on recognition of stimuli from the left and right visual fields.

Two experiments examined the effect of concurrently holding 0, 2, 4, or 6 nouns in memory on the recognition of visual stimuli briefly presented to the left or right visual fields. When stimuli to be visually recognized were complex visuospatial forms it was found that a relatively easy memroy load of 2 or 4 nouns improved visual recognition accuracy on right visual field (left-hemisphere) trials relative to the no-memory condition; however, a more difficult memory load of 6 nouns decreased visual recognition accuracy to a level slightly below the no-memory condition. There were no effects of concurrent verbal memroy on visual form recognition on left visual field (right-hemisphere) trials. When the stimuli to be visually recognized were words it was found that a relatively easy memroy load of 2 or 4 nouns improved visual recognition accuracy and a more difficult load of 6 nouns decreased visual recognition accuracy on both left and right visual field trials. The complete pattern of results indicates that several factors including cerebral hemisphere specialization, stimulus codability, selective perceptual orientation, and selective cerebral hemisphere interference interact in systematic ways to produce overall visual laterality effects.     

Generation of visual representations

The visual confusability of uppercase letters was manipulated in a successive same-different task to study the conditions under which visual generation from auditory inputs would occur and to investigate the figural specificity of the generated representations. Prior experiments have shown that visual confusions do occur when the initial stimulus is auditory and the second one is visual, which indicates that auditory stimuli can be encoded into visual forms. There has been some suggestion, however, that the generated visual code may have been too abstract to differentiate between the two cases in which letters can appear. In the present experiment, although the confusion effect was not eliminated when the subjects had no advance knowledge regarding the case in which the visual stimulus would appear, the marked confusion effect obtained when the visual stimulus was an uppercase letter was substantially attenuated when the letter appeared in lowercase. This was taken to indicate that the visual characteristics of a generated visual representation may be relatively specific. The results also suggested that subjects may wait until after the second stimulus is presented before they generate the visual representation of the initial auditory stimulus.     

不同深度平面与表面的视知觉完形加工

以往有关视觉完形加工的研究主要探索同一深度平面内的相似纹理表面或相关轮廓特性等对完形加工的影响。该研究采用汉字碎块,考察了双眼视差、颜色以及遮挡等线索在视觉完形中的作用。发现结果如下：视差与颜色等线索阻碍了视觉完形加工;遮挡线索加速了整体的视觉完形形成;在高级认知加工参与下,遮挡线索有效抑制了视差、颜色等线索的分离作用。通过对知觉填补机制及其理论的讨论,可以认为,该研究结果为不同深度平面间的视知觉完形加工提供了实验支持。     

Visual perception in 'low vision'

'Low vision' has an international classification as an impairment of vision that is defined by loss of visual acuity and the size of the visual field. Functional classification that would depict capability to use vision in different activities has not yet been agreed upon. Abnormal visual information leads to changes in visual perception, and brain-damage-related visual impairment may alter or prevent one or several cognitive visual functions. Abnormal visual perception opens a window into brain mechanisms that the psychophysicists otherwise do not have. Together with clinicians, psychophysicists can help visually impaired persons to understand the nature of their disability by thoroughly studying the nature of the altered image and the profile of cognitive visual functions.     

Rapid learning in attention shifts: A review

Many lines of evidence show that the human visual system does not simply passively register whatever appears in the visual field. The visual system seems to preferentially “choose” stimuli according to what is most relevant for the task at hand, a process called attentional selection. Given the large amount of information in any given visual scene, and well-documented capacity limitations for the representation of visual stimuli, such a strategy seems only reasonable. Consistent with this, human observers are surprisingly insensitive to large changes in their visual environment when they attend to something else in the visual scene. Here I argue that attentional selection of pertinent information is heavily influenced by the stimuli most recently viewed that were important for behaviour. I will describe recent evidence for the existence of a powerful memory system, not under any form of voluntary control, which aids observers in orienting quickly and effectively to behaviourally relevant stimuli in the visual environment, in particular the stimuli that have been important in the immediate past. I will also discuss research into the potential neural mechanisms involved in these learning effects. Finally, I will discuss how these putative memory mechanisms may help in maintaining the apparent stability and continuity of the ever-changing visual environment, which is such a crucial component of our everyday visual experience.     

Interference in Visual Working Memory

This paper uses the theoretical distinction that has recently developed between the passive visual store and the active spatial rehearsal mechanism of the visuo-spatial component of working memory (VSSP). It examines the circumstances under which visual fields gain functional access to the passive visual store and seeks to cast light on the circumstances under which irrelevant visual fields interfere with concurrent visual processing. Experiment 1 contrasts a dynamic visual noise field with a static noise field and shows that the static field, in contrast to the dynamic noise field, causes no interference when presented concurrently with a visual task. Experiment 2 investigates the reason for this contrast and concludes that the static field is susceptible to decay and so fails to cause interference. Experiment 3 investigates further the circumstances under which dynamic visual noise causes interference and shows that manipulation of the number of changes within the noise field is also of importance in causing interference. The results allow further consideration of the characteristics of the VSSP.     

Experience and information loss in auditory and visual memory

Recent studies show that recognition memory for sounds is inferior to memory for pictures. Four experiments were conducted to examine the nature of auditory and visual memory. Experiments 1–3 were conducted to evaluate the role of experience in auditory and visual memory. Participants received a study phase with pictures/sounds, followed by a recognition memory test. Participants then completed auditory training with each of the sounds, followed by a second memory test. Despite auditory training in Experiments 1 and 2, visual memory was superior to auditory memory. In Experiment 3, we found that it is possible to improve auditory memory, but only after 3 days of specific auditory training and 3 days of visual memory decay. We examined the time course of information loss in auditory and visual memory in Experiment 4 and found a trade-off between visual and auditory recognition memory: Visual memory appears to have a larger capacity, while auditory memory is more enduring. Our results indicate that visual and auditory memory are inherently different memory systems and that differences in visual and auditory recognition memory performance may be due to the different amounts of experience with visual and auditory information, as well as structurally different neural circuitry specialized for information retention.     

Visual space as physical geometry

The geometrical incongruence between patterns in visual space and structures and patterns of activity in the visual cortex, long known to investigators, serves as a criterion for evaluating physical theories of visual space. The problem of determining the geometry of the visual world (visual geometry) is compared with that of determining the geometry of the physical world (physical geometry). Theories as to the possible physical locus of visual space, whether in the brain or elsewhere, are reviewed, analyzed, and criticized accordingly. It is concluded that on the basis of congruence alone it would be predicted that visual space is not to be found in the brain, even though it is seemingly linked to it causally, as experimental neurology and neurophysiology demonstrate. Alternative theories as to the nature of visual space are considered, but are also found to be inadequate in explaining visual space in terms acceptable to contemporary science.     

Predictive and postdictive mechanisms jointly contribute to visual awareness

One of the fundamental issues in visual awareness is how we are able to perceive the scene in front of our eyes on time despite the delay in processing visual information. The prediction theory postulates that our visual system predicts the future to compensate for such delays. On the other hand, the postdiction theory postulates that our visual awareness is inevitably a delayed product. In the present study we used flash-lag paradigms in motion and color domains and examined how the perception of visual information at the time of flash is influenced by prior and subsequent visual events. We found that both types of event additively influence the perception of the present visual image, suggesting that our visual awareness results from joint contribution of predictive and postdictive mechanisms.     

Evidence against visual integration across saccadic eye movements

One of the classic problems in perception concerns how we perceive a stable, continuous visual world even though we view it via a temporally discontinuous series of eye movements. Previous investigators have suggested that our perception of a stable visual environment is due to anintegrative visual buffer, a special memory store capable of fusing the visual contents of successive fixations according to their environmental coordinates. In this paper, three experiments are reported that attempted to demonstrate the existence of an integrative visual buffer. The experimental procedure required subjects to mentally fuse two halves of a dot matrix presented in the same spatial region of a display, but separated by an eye movement so that each half was viewed only during one fixation. Thus, subjects had to integrate packets of visual information that had the same environmental coordinates, but different retinal coordinates. No evidence was found in any experiment for the fusion of visual information from successive fixations in memory, leaving the status of the integrative visual buffer in serious doubt.     

Visual Art and the Rhythm of Experience

The concept of rhythm is frequently used by art historians, critics, and philosophers as a way of describing central features of visual art. Since rhythm is generally considered to be a temporal phenomenon associated with music, it is far from clear how visual art, composed of fixed lines, figures, and color, can be associated with rhythmicity. Linked to a temporal ordering or structure in music, the notion of rhythm in visual art leads to a claim that the aesthetic aspect of a painting does not consist in, or emerge from, its spatial structures, but rather its temporal ordering of the visual field. Recently this account of rhythm in visual art has been criticized by philosopher Jason Gaiger, who argues that visual art does not comprise movement and therefore cannot be associated with a temporal rhythm. Through a discussion of temporality and rhythm in Edmund Husserl, Erwin Straus, and Henri Maldiney, this article maintains that rhythmicity is a central aspect of experiences with visual art. It is shown that the phenomenological account of rhythm in the experience of visual art is fundamentally linked to a different notion of time.     

Dynamic visual noise interferes with storage in visual working memory

Several studies have demonstrated that dynamic visual noise (DVN) does not interfere with memory for random matrices. This has led to suggestions that (a) visual working memory is distinct from imagery, and (b) visual working memory is not a gateway between sensory input and long-term storage. A comparison of the interference effects of DVN with memory for matrices and colored textures shows that DVN can interfere with visual working memory, probably at a level of visual detail not easily supported by long-term memory structures or the recoding of the visual pattern elements. The results support a gateway model of visuospatial working memory and raise questions about the most appropriate ways to measure and model the different levels of representation of information that can be held in visual working memory.     

Visual memory and stimulus repetition effects

Recent investigations of memory for randomly configured patterns indicate that visual memory can involve distinct short-term and long-term components. The appearance of a visual recency effect that is confined to the last-presented item is believed to result from the active visualization of this item during the retention interval. Studies of the retention of familiar visual information have also suggested that the short-term effects observed are a result of active visualization. In a review of these studies, however, we argue that the effects obtained with familiar visual information are not necessarily a result of active visualization and, indeed, may not involve anything other than long-term visual memory. For example, Rabbitt and Vyas (1979) observed a visual recency effect in a serial choice reaction time task involving familiar information. That this recency effect was confined to the final item accords with the results obtained with unfamiliar visual information. However, this choice reaction time task did not require subjects to remember previous stimuli, so it is unlikely that they actively visualized them. With the case for a distinct short-term visual memory currently resting on the recency effect interpreted as reflecting a process of active visualization, this result is especially important. In the second part of the present paper, we report a series of experiments that provides an understanding of the visual recency effect in the serial choice reaction time task. We conclude from these studies that this effect is not due to visualization or to a visual trace either decaying or being overwritten by a succeeding stimulus.     

Interaction between visually and kinesthetically triggered voluntary responses

A voluntary motor response that is prepared in advance of a stimulus may be triggered by any sensory input. This study investigated the combination of visual and kinesthetic inputs in triggering voluntary torque responses. When a visual stimulus was presented alone, subjects produced a fast and accurate increase in elbow flexion torque. When a kinesthetic stimulus was presented instead of the visual stimulus, subjects produced a similar response with a reduced response latency. When a visual stimulus was presented in combination with a kinesthetic stimulus, subjects initiated their responses after either a visual or a kinesthetic response latency, depending on the relative timing of the two stimuli. An analysis of response amplitude suggested that when visual and kinesthetic stimuli were combined, both stimuli triggered a response. The results are more consistent with a simple behavioral model of addition of visual and kinesthetic responses (which predicts that the response to combined stimuli should be the sum of individual responses) than with a model of exclusion of one response (which predicts that the response to combined stimuli should be identical to either the visual or the kinesthetic response). Because addition of visually and kinesthetically triggered responses produced a response with an erroneously large amplitude, it is suggested that visual and kinesthetic inputs are not always efficiently integrated.     

Discrete Visual Samples May Control Locomotor Equilibrium and Foot Positioning in Man

The static or dynamic visual cues required for equilibrium as well as for foot guidance in visually guided locomotion in man were studied using a variety of locomotion supports and illumination and visual conditions. Stroboscopic illumination (brief flashes) and intermittent lighting (longer flashes) were used to control and to vary the visual sampling frequency of static (positional/orientational) visual cues. There were three main findings: First, visual control of foot positioning during locomotion over discontinuous terrain depends mainly upon static visual cues with a low sampling frequency (about 3 Hz); second, visual control of dynamic equilibrium during locomotion over a narrow support depends mainly upon the availability of high frequency static visual cues (up to about 12 Hz); and third, static visual cues required for equilibrium control are extracted from both the peripheral and the central visual field.

Assuming that discrete demands for feedback occur, a simple probabilistic model was proposed, according to which the mean time that elapses following presentation of static visual cues about positions or changes of position accounts for the differences in the difficulty of the various illumination conditions.