Identification of scanned and static tactile patterns

Most of the studies in which the interactions between target and nontarget spatial patterns have been examined have tested patterns that are generated statically. Static patterns are those in which all the elements of the pattern are presented at the same time and at a fixed location on the skin; however, most tactile information comes to the skin by means of patterns' being scanned across the surface of the skin. In the present study, the interactions between target and nontarget patterns were measured for patterns generated in both the static and the scanned modes. Nontarget patterns often interfere with the perception of target patterns. Using patterns generated in the static mode, previous studies have identified two factors that produce interference in pattern identification: response competition and masking. Masking, in turn, appears to be the result of temporal integration of the target and nontarget patterns, as well as the displacement of target features. In the present study, these factors were examined for patterns generated in both static and scanned modes. Regardless of the mode in which the patterns were generated, similar functions were obtained relating identification performance to the temporal separation between the target and the nontarget patterns. Although statically generated patterns are more easily identified than scanned patterns, particularly at brief durations, mechanisms such as response competition, temporal integration, and the displacement of target features appear to be factors that affect scanned patterns to nearly the same degree as static patterns.     

Two-pulse temporal integration functions in the fovea and peripheral retina

The temporal integration of luminous energy was compared in the fovea and at 7 degrees eccentricity using two-pulse stimuli and two methodologies. The two-pulse stimuli consisted of two 1-msec. light pulses separated by intervals of darkness ranging from 1 to 400 msec.; they were provided by a glow modulator tube transilluminating a 21.8' opal glass target. In Exp. 1 (equal-performance design), integration functions were generated using a forced-choice staircase procedure to estimate threshold luminance. The data for two Os showed that the critical duration (CD), and thus the period of complete integration, was briefer in the fovea than at 7 degrees. Beyond the CD, integration continued to differ for the two retinal locations. In the fovea, two-pulse stimuli beyond CD evidenced partial integration and at the longest stimulus durations no integration or inhibition. In contrast, at 7 degrees stimuli beyond CD appeared to evidence probability summation. In Exp. 2 (equal-energy design), integration functions were generated by measuring the detectability of two-pulse stimuli of different durations but equal in total luminous energy. A signal-detection procedure yielded measures of both response frequency and signal detectability, P(A). The data for two Os showed that for both measures CD was briefer in the fovea than at 7 degrees. Also, in the fovea, long two-pulse stimuli appeared to show no integration or inhibition. Both experiments then showed a foveal-peripheral difference in two-pulse measures of visual temporal integration, with the fovea evidencing less integration. In addition, the forced-choice and signal-detection procedures showed that these loci differences in integration were independent of the Os' response criterion.     

Mechanisms of percept-percept and image-percept integration in vision: behavioral and electrophysiological evidence

Previous research has shown that the detection of a visual target can be guided not only by the temporal integration of two percepts, but also by integrating a percept and an image held in working memory. Behavioral and event-related brain potential (ERP) measures were obtained in a target detection task that required temporal integration of 2 successively presented stimuli in the left or right hemifield. Task performance was good when both displays followed each other immediately (percept-percept integration) and when displays were separated by a 300- or 900-ms interval (image-percept integration), but was poor with intermediate interstimulus intervals. An enhanced posterior negativity at electrodes contralateral to the side of the target was observed for percept-percept and for image-percept integration, demonstrating that both are based on spatiotopic representations. However, this contralateral negativity emerged later and was more sustained on trials with long interstimulus intervals, indicating that image-percept integration is slower and involves a sustained activation of working memory.     

The effects of Kanizsa contours on temporal integration and attention in rapid serial visual presentation

Performance in rapid serial visual presentation tasks has been shown to depend on the temporal integration of target stimuli when they are presented in direct succession. Temporal target integration produces a single, combined representation of visually compatible stimuli, which is comparatively easy to identify. It is currently unknown to what extent target compatibility affects this perceptual behavior, because it has not been studied systematically to date. In the present study, the effects of compatibility on temporal integration and attention were investigated by manipulating the Gestalt properties of target features. Of particular interest were configurations in which a global illusory shape was formed when all stimulus features were present; a Kanizsa stimulus, which was expected to have a unifying effect on the perception of the successive targets. The results showed that although the presence of a Kanizsa shape can indeed enhance temporal integration, this also was observed for other good Gestalts, such as due to common fate and closure. Identification accuracy seemed to vary, possibly as a result of masking strength, but this did not seem associated with attentional processing per se. Implications for theories of Gestalt processing and temporal integration are discussed.     

A purely temporal transparency mechanism in the visual system.

I report evidence for a purely temporal perceptual transparency mechanism. Rapid alternation of two images in the same location can result in the simultaneous experience of both, accompanied by a sense of transparency. This is true even when the sum of the two images does not appear transparent, which suggests that the percept is not mediated by the static transparency processes. At slow rates, alternating gratings were experienced as successive. As the rate was increased, by 8 Hz observers experienced the gratings as simultaneous. The rapidly alternating gratings are apparently processed separately before being combined for awareness by a process that integrates over about 120 ms. A final experiment tested whether the common presentation time of different parts of an image in alternation with another would cause the parts to perceptually bind. Observers did not distinguish between a rapidly alternating intact grating display and one in which halves of the display were exchanged in time. In other words, temporal binding across space did not occur. The temporal transparency phenomenon, in addition to informing theories of transparency and the dynamics of visual processing, may also be useful for the creation of transparent displays for electronic devices.     

Stream/bounce perception and the effect of depth cues in chimpanzees (Pan troglodytes)

The stream/bounce display represents an ambiguous motion event in which two identical visual objects move toward one another and the objects overlap completely before they pass each another. In our perception, they can be interpreted as either streaming past one another or bouncing off each other. Previous studies have shown that the streaming percept of the display is generic for humans, suggesting the inertial nature of the motion integration process. In this study, chimpanzees took part in behavioral experiments using an object-tracking task to reveal the characteristics of their stream/bounce perception. Chimpanzees did not show a tendency toward a dominant "stream" perception of the stream/bounce stimulus. However, depth cues, such as X-junctions and local motion coherence, did promote the stream percept in chimpanzees. These results suggest both similarities and differences between chimpanzees and humans with respect to motion integration and object individuation processes.     

Do noise masks terminate target processing?

Much recent research in visual information processing has employed a methodology resting on the assumption that a noise mask following presentation of a target stimulus terminates processing of that target. In the absence of appropriate controls, such a methodology is viable only insofar as an erasure theory of masking is valid. However, the phenomena from which the erasure position has derived its strongest support have been subject to alternative theoretical explanations, the most general of which is that of temporal integration. The experiment reported here tested these alternatives. Twelve subjects served in a tachistoscopic study designed to determine whether the same noise field of dots could either erase a degraded target digit or facilitate target identification through temporal integration, under both forward and backward masking paradigms. This was found to be the case, and the results were interpreted as consistent with an integration theory of masking and as incompatible with an erasure conception. The results suggested that efforts to control target processing time through display of a visual noise pattern subsequent to target presentation are methodologically inadequate when devoid of some basic control operations.     

Temporal factors in the discrimination of coherent motion

When observers view the relative movements of a pair of bars defined by the difference of spatial Gaussian functions (DOGs), they can accurately discriminate coherent movements over a range of temporal frequencies and temporal asynchronies. Of particular interest is the fact that performance accuracy is maintained even when the two bars differ in spatial-frequency content and contrast. On each trial, observers viewed two brief presentation intervals in which a pair of vertically oriented DOGs moved randomly back and forth within a restricted range. During one observation interval, both elements moved in the same direction and by the same magnitude (correlated), and in the other interval, the movements were independent (uncorrelated). Temporal asynchronies were introduced by delaying the displacement of the right bar relative to that of the left bar in each interval. Observers were able to discriminate correlated versus uncorrelated movements up to a 45–60-msec temporal delay between the two elements’ relative displacements. If motion processing is accomplished by mechanisms operating over multiple spatial and temporal scales, the visual system’s tolerance of temporal delays among correlated signals may facilitate their space-time integration, thereby capitalizing on the perceptual utility of coherent-motion information for image segmentation and interpolating surface structure from the movements of spatially separated features.     

Temporal factors in the discrimination of coherent motion.

When observers view the relative movements of a pair of bars defined by the difference of spatial Gaussian functions (DOGs), they can accurately discriminate coherent movements over a range of temporal frequencies and temporal asynchronies. Of particular interest is the fact that performance accuracy is maintained even when the two bars differ in spatial-frequency content and contrast. On each trial, observers viewed two brief presentation intervals in which a pair of vertically oriented DOGs moved randomly back and forth within a restricted range. During one observation interval, both elements moved in the same direction and by the same magnitude (correlated), and in the other interval, the movements were independent (uncorrelated). Temporal asynchronies were introduced by delaying the displacement of the right bar relative to that of the left bar in each interval. Observers were able to discriminate correlated versus uncorrelated movements up to a 45-60-msec temporal delay between the two elements' relative displacements. If motion processing is accomplished by mechanisms operating over multiple spatial and temporal scales, the visual system's tolerance of temporal delays among correlated signals may facilitate their space-time integration, thereby capitalizing on the perceptual utility of coherent-motion information for image segmentation and interpolating surface structure from the movements of spatially separated features.     

Effects of temporal integration on the shape of visual backward masking functions

Many studies of cognition and perception use a visual mask to explore the dynamics of information processing of a target. Especially important in these applications is the time between the target and mask stimuli. A plot of some measure of target visibility against stimulus onset asynchrony is called a masking function, which can sometimes be monotonic increasing but other times is U-shaped. Theories of backward masking have long hypothesized that temporal integration of the target and mask influences properties of masking but have not connected the influence of integration with the shape of the masking function. With two experiments that vary the spatial properties of the target and mask, the authors provide evidence that temporal integration of the stimuli plays a critical role in determining the shape of the masking function. The resulting data both challenge current theories of backward masking and indicate what changes to the theories are needed to account for the new data. The authors further discuss the implication of the findings for uses of backward masking to explore other aspects of cognition.     

Visual masking plays two roles in the attentional blink

When two targets are displayed in rapid visual sequence and masked by trailing patterns, identification accuracy is nearly perfect for the first target but follows a U-shaped pattern over temporal lag for the second target. Three experiments examined the role of visual masking in this attentional blink. Experiment 1 compared integration and interruption masks for both targets. Although either mask was effective in producing the blink when applied to the first target, only the interruption mask was effective when applied to the second target. Experiment 2 showed that integration masking of the second target was ineffective over a wide range of accuracy levels. Combining the two forms of masking in Experiment 3 confirmed the dissociation: A combined mask and only a main effect on accuracy for the first target, whereas it produced a qualitatively different pattern over temporal lag for the second target. These results suggest that representations of the target are substituted in consciousness by that of the interruption mask when visual attention is preoccupied.     

Temporal integration of spatially filtered visual images.

Factors which govern the temporal integration of spatial information were examined in a group of five experiments. A series of high-pass and low-pass spatially filtered versions of a visual scene were generated. Observers' ratings of these filtered versions of the scene for perceived image quality indicated that quality was determined both by the bandwidth of spatial information and the presence of high-spatial-frequency edge information. When sequences of three different versions of the scene were presented over an interval of 120 ms the perceived quality of the resulting composite image was determined both from the ratings of the individual components of that sequence and from the order in which these components were presented. When the order of spatial information in a sequence moved from coarse to fine detail the perceived quality of the composite image was significantly better than when the order moved from fine to coarse. This evidence of a coarse-to-fine bias in pattern integration was further investigated with a detection paradigm. The pattern of errors once again indicated that temporal integration of spatial information was superior when a coarse-to-fine mode of information delivery was employed. Taken together the data indicate that the pattern-integration mechanism has an inherent order bias and does not accumulate spatial information so efficiently when the 'natural' coarse-to-fine order is violated.     

Adaptive control of event integration

Identifying 2 target stimuli in a rapid stream of visual symbols is much easier if the 2nd target appears immediately after the 1st target (i.e., at Lag 1) than if distractor stimuli intervene. As this phenomenon comes with a strong tendency to confuse the order of the targets, it seems to be due to the integration of both targets into the same attentional episode or object file. The authors investigated the degree to which people can control the temporal extension of their (episodic) integration windows by manipulating the expectations participants had with regard to the time available for target processing. As predicted, expecting more time to process increased the number of order confusions at Lag 1. This was true for between-subjects and within-subjects (trial-to-trial) manipulations, suggesting that integration windows can be adapted actively and rather quickly.     

音标-音素意识整合训练的重要价值——小学二年级干预组与三年级对照组的比较

采用前-后测对照组的准实验设计,通过小学二年级的两个干预组与小学三年级的一个对照组之间的比较研究,结果表明:音标知识、音素分解、合成、删除与替换技能相整合的训练方案,以及音标知识、音素分解与合成技能相整合的训练方案,都有利于提高小学二年级学生的英语音素意识、准朗读和朗读技能;不过,训练内容相对多的前者,并没有显著地优于训练内容相对少的后者。     

Quantifying temporal ventriloquism in audiovisual synchrony perception

The integration of visual and auditory inputs in the human brain works properly only if the components are perceived in close temporal proximity. In the present study, we quantified cross-modal interactions in the human brain for audiovisual stimuli with temporal asynchronies, using a paradigm from rhythm perception. In this method, participants had to align the temporal position of a target in a rhythmic sequence of four markers. In the first experiment, target and markers consisted of a visual flash or an auditory noise burst, and all four combinations of target and marker modalities were tested. In the same-modality conditions, no temporal biases and a high precision of the adjusted temporal position of the target were observed. In the different-modality conditions, we found a systematic temporal bias of 25–30 ms. In the second part of the first and in a second experiment, we tested conditions in which audiovisual markers with different stimulus onset asynchronies (SOAs) between the two components and a visual target were used to quantify temporal ventriloquism. The adjusted target positions varied by up to about 50 ms and depended in a systematic way on the SOA and its proximity to the point of subjective synchrony. These data allowed testing different quantitative models. The most satisfying model, based on work by Maij, Brenner, and Smeets (Journal of Neurophysiology 102, 490–495, 2009), linked temporal ventriloquism and the percept of synchrony and was capable of adequately describing the results from the present study, as well as those of some earlier experiments.     

The use of chromatic information for motion segmentation: differences between psychophysical and eye-movement measures

Previous psychophysical studies have shown that chromatic (red/green) information can be used as a segmentation cue for motion integration. We investigated the mechanisms mediating this phenomenon by comparing chromatic effects (and, for comparison, luminance effects) on motion integration between two measures: (i) directional eye movements with the notion that these responses are mediated mainly by low-level motion mechanisms, and (ii) psychophysical reports, with the notion that subjects' reports should employ higher-level (attention-based) mechanisms if available. To quantify chromatic (and luminance) effects on motion integration, coherent motion thresholds were obtained for two conditions, one in which the signal and noise dots were the same 'red' or 'green' chromaticity (or the same 'bright' or 'dark' luminance), referred to as homogeneous, and the other in which the signal and noise dots were of different chromaticities (or luminances), referred to as heterogeneous. 'Benefit ratios' (theta(HOM)/theta(HET)) were then computed, with values significantly greater than 1.0 indicating that chromatic (or luminance) information serves as a segmentation cue for motion integration. The results revealed a high and significant chromatic benefit ratio when the measure was based on psychophysical report, but not when it was based on an eye-movement measure. By contrast, luminance benefit ratios were roughly the same (and significant) for both measures. For comparison to adults, eye-movement data were also obtained from 3-month-old infants. Infants showed marginally significant benefit ratios in the luminance, but not in the chromatic, condition. In total, these results suggest that the use of chromatic information as a segmentation cue for motion integration relies on higher-level mechanisms, whereas luminance information works mainly through low-level motion mechanisms.     

中文阅读中的边界效应及其消除：事件持续效应

运用动窗技术探讨中文阅读中的边界效应及其消除的条件,包括3个实验。实验一探讨中文阅读中是否存在边界效应,结果发现,边界效应同样存在于中文阅读中;实验二、三探讨时间切分标记能否消除边界效应以及消除的条件,结果发现,只有当切分标记表示的时间在前一事件持续的时间跨度外时才能消除边界效应,如果切分标记表示的时间仍在前一事件持续的时间跨度内,则不能消除边界效应,本研究称此为事件持续效应。从本研究结果中可以得出,时间切分标记降低了主题转换句子所需要的认知加工能量     

Inferring action structure and causal relationships in continuous sequences of human action

In the real world, causal variables do not come pre-identified or occur in isolation, but instead are embedded within a continuous temporal stream of events. A challenge faced by both human learners and machine learning algorithms is identifying subsequences that correspond to the appropriate variables for causal inference. A specific instance of this problem is action segmentation: dividing a sequence of observed behavior into meaningful actions, and determining which of those actions lead to effects in the world. Here we present a Bayesian analysis of how statistical and causal cues to segmentation should optimally be combined, as well as four experiments investigating human action segmentation and causal inference. We find that both people and our model are sensitive to statistical regularities and causal structure in continuous action, and are able to combine these sources of information in order to correctly infer both causal relationships and segmentation boundaries.     

Using movement and intentions to understand simple events

In order to understand ongoing activity, observers segment it into meaningful temporal parts. Segmentation can be based on bottom-up processing of distinctive sensory characteristics, such as movement features. Segmentation may also be affected by top-down effects of knowledge structures, including information about actors’ intentions. Three experiments investigated the role of movement features and intentions in perceptual event segmentation, using simple animations. In all conditions, movement features significantly predicted where participants segmented. This relationship was stronger when participants identified larger units than when they identified smaller units, and stronger when the animations were generated randomly than when they were generated by goal-directed human activity. This pattern suggests that bottom-up processing played an important role in segmentation of these stimuli, but that this was modulated by top-down influence of knowledge structures. To describe accurately how observers perceive ongoing activity, one must account for the effects of distinctive sensory characteristics, the effects of knowledge structures, and their interactions.     

Temporal integration between visual images and visual percepts

Using a temporal integration task, subjects in 5 experiments were expected to combine information from temporally separated visual presentations. Evidence from these experiments indicated that perceptual information can be integrated with previously generated and currently maintained visual images to form a representation that contains information from each source. Properties and limitations of this integration process were also explored, including the time required to generated the image, the speed at which percepts were integrated with images, and the capacity of the representation. Implications for theories of visual processing and memory are discussed.