注意促进运动知觉判断的时间进程

本研究通过控制深度视觉线索, 分析3D SFM (structure from motion)知觉中的眼动特征, 探讨注意对SFM知觉判断的影响及其时间进程。结果显示, 有线索刺激比模糊刺激的判断更加快、更加肯定(百分比更高); 眼睛移动方向和微眼跳方向都分别与知觉判断的运动方向具有一致性; 微眼跳频次、峰速度和幅度也都分别表现出深度线索的促进效应。实验结果表明, SFM知觉过程大致分为速度计算和构建三维结构两个阶段; 注意对SFM知觉的调节作用主要发生在构建三维结构阶段; 注意从150 ms开始指向选择对象, 驻留持续约200 ms后, 从局部运动矢量流转移到整体运动方向的知觉判断。     

The efficiency of biological motion perception

Humans can readily perceive biological motion from point-light (PL) animations, which create an image of a moving human figure by tracing the trajectories of a small number of light points affixed to a moving human body. We have applied ideal observer analysis to a standard biological motion discrimination task involving either full-figure or PL displays. Contrary to current dogma, we find that PL animations can be rich inpotential stimulus information but that human observers are remarkably inefficient at exploiting this information. Although our findings do not discount the utility of PL animation, they do provide a realistic measure of the computational challenge posed by biological motion perception.     

How to keep a reversible figure from reversing: teasing out top-down and bottom-up processes

The nature of processes underlying our perception of reversible figures was examined through two experiments investigating the effects of prior exposure conditions on an observer's report of figural reversal. In experiment 1, observers were adapted over several minutes to an unambiguous version of a rotating Necker cube prior to the presentation of the standard ambiguous figure. Results indicated that adaptation produced an immediate bias to perceive the ambiguous figure in the opposite configuration (ie reverse bias) and to reduce reports of reversal over the test period. The introduction of a brief delay between the adaptation and test periods revealed that this bias is a highly transient effect and is only clearly evident when the adaptation and test figures are matched in size. In experiment 2, observers were primed with an unambiguous figure for a few seconds prior to the presentation of the standard ambiguous figure. In this case, the obtained bias strongly favored the observer's reporting the ambiguous figure to be in the same configuration as the adapting figure (ie positive bias); and neither introducing a delay period nor changing figure size had any effect. We conclude that these experiments reveal the distinct roles of transient, retinally localized neural processes as well as more stable, global processes under specifiable conditions.     

Adaptation to spiral motion in crowding condition

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

Motion induction from biological motion

A new type of motion illusion is described in which ambiguous motion becomes unidirectional on superimposition of a human figure walking on a treadmill. A point-light walker in profile was superimposed on a vertical counterphase grating backdrop. Eleven na?ve observers judged the apparent direction of motion against the grating as left or right in a two-alternative forced-choice task and found that the grating appeared to drift in a direction opposite to the walking. The illusion disappeared when the point lights moved in scrambled configurations. This indicates that the illusion is caused by biological motion that provides recognition of gaits. A human figure walking backwards produced no illusion because of the difficulty in identifying the gait. This indicates that the illusion is determined by translational motion rather than form represented from biological motion.     

Activations of "motor" and other non-language structures during sentence comprehension

In this paper we report the results of an experiment in which subjects read syntactically unambiguous and ambiguous sentences which were disambiguated after several words to the less likely possibility. Understanding such sentences involves building an initial structure, inhibiting the non-preferred structure, detecting that later input is incompatible with the initial structure, and reactivating the alternative structure. The ambiguous sentences activated four areas more than the unambiguous sentences. These areas are the left inferior frontal gyrus (IFG), the right basal ganglia (BG), the right posterior dorsal cerebellum (CB) and the left median superior frontal gyrus (SFG). The left IFG is normally activated when syntactic processing complexity is increased and probably supports that function in the current study as well. We discuss four hypotheses concerning how these areas may support comprehension of syntactically ambiguous sentences. (1) The left IFG, right CB and BG could support articulatory rehearsal used to support the processing of ambiguous sentences. This seems unlikely since the activation pattern associated with articulatory rehearsal in other studies is not similar to that seen here. (2) The CB acts as an error detector in motor processing. Error detection is important for recognizing that the wrong sentence structure has been chosen initially. (3) The BG acts to select and sequence movements in the motor domain and in cognitive domains may serve to inhibit competing and completed plans which is not unlike inhibiting the initially non-preferred structure or "unchoosing" the initial choice when incompatible syntactic input is received. (4) The left median SFG is relevant for the evaluation of plausibility. Evaluating the plausibility of the two possibilities provides an important basis for choosing between them. The notion of the use of domain general cognitive processes to support a linguistic process is in line with recent suggestions that the a given area may subserve a specific cognitive task because it carries out an appropriate sort of computation rather than because it supports a specific cognitive domain.     

Perceiving human locomotion: priming effects in direction discrimination

During the perception of biological motion, the available stimulus information is confined to a small number of lights attached to the major joints of a moving actor. Despite this drastic impoverishment of the stimulus, the human visual apparatus organizes the swarm of moving dots in a vivid percept of a human figure. In addition, observers effortlessly identify the action the figure is involved in. After a historical introduction and a short walk through the literature, data from a priming experiment are presented. In a serial two-choice reaction-time task, participants were presented with a point-light walker, facing either to the right or to the left and walking either forward or backward on a treadmill. Subjects had to identify the direction of articulatory movements. Reliable priming effects were established in consecutive trials, but these effects were tempered by the relation between priming and primed walker. The reaction time to a walker was shorter when the walker in the preceding trial moved in the same direction and was facing in the same direction. The findings are discussed in relation to recent data from neuropsychological case studies, neuroimaging, and single-cell recording.     

Consciousness mediated by neural transition states: How invisibly rapid motions can become visible

When observers view a rapidly moving stimulus they may see only a static streak. We report that there can be a transient percept of motion if such a moving stimulus is preceded or followed by a stationary image of that stimulus. A ring of dots was rotated so rapidly observers only saw a continuous outline circle and could not report its rotation direction. When an objectively stationary ring of dots preceded or followed this rotating ring, the stationary ring appeared to visibly launch into motion from a standstill or visibly rotate to a halt, principally in the same direction as the actual rapid rotation. Thus, motions too rapid to be consciously perceived as motion can nonetheless be processed by the visual system, and generate neural transition states that are consciously experienced as motion percepts. We suggest such transition states might serve a unifying function by bridging discontinuous motion states.     

Shallow processing of ambiguous pronouns: Evidence for delay

Two self-paced reading-time experiments examined how ambiguous pronouns are interpreted under conditions that encourage shallow processing. In Experiment 1 we show that sentences containing ambiguous pronouns are processed at the same speed as those containing unambiguous pronouns under shallow processing, but more slowly under deep processing. We outline three possible models to account for the shallow processing of ambiguous pronouns. Two involve an initial commitment followed by possible revision, and the other involves a delay in interpretation. In Experiment 2 we provide evidence that supports the delayed model of ambiguous pronoun resolution under shallow processing. We found no evidence to support a processing system that makes an initial commitment to an interpretation of the pronoun when it is encountered. We extend the account of pronoun resolution proposed by Rigalleau, Caplan, and Baudiffier (2004) to include the treatment of ambiguous pronouns under shallow processing.     

Shallow processing of ambiguous pronouns: evidence for delay

Two self-paced reading-time experiments examined how ambiguous pronouns are interpreted under conditions that encourage shallow processing. In Experiment 1 we show that sentences containing ambiguous pronouns are processed at the same speed as those containing unambiguous pronouns under shallow processing, but more slowly under deep processing. We outline three possible models to account for the shallow processing of ambiguous pronouns. Two involve an initial commitment followed by possible revision, and the other involves a delay in interpretation. In Experiment 2 we provide evidence that supports the delayed model of ambiguous pronoun resolution under shallow processing. We found no evidence to support a processing system that makes an initial commitment to an interpretation of the pronoun when it is encountered. We extend the account of pronoun resolution proposed by Rigalleau, Caplan, and Baudiffier (2004) to include the treatment of ambiguous pronouns under shallow processing.     

Priming by motion too rapid to be consciously seen

When a rapidly rotating ring of dots was briefly flashed, observers saw only a solid ring with no discriminable rotation. However, when this stimulus served as a prime that was followed by a target that consisted of a clearly rotating ring of dots, response times (RTs) to report the target's rotation were shorter when the prime and target directions were congruent than when they were incongruent. In accord with shape priming data, this priming effect increased monotonically with the prime-target stimulus-onset asynchrony (SOA). The prime also biased the perceived direction of an ambiguous apparent motion target, but only at an intermediate SOA. At the same SOA, we also found that target presentations enabled above-chance discrimination of prime's rotation direction. These outcomes demonstrate the processing of motion direction information that is not phenomenally represented. They suggest a common mechanism may mediate the priming of RTs by shape and motion, whereas a different mechanism mediates perceptual measures of motion priming.     

The role of mask coherence in motion-induced blindness

Motion-induced blindness (MIB) is the perceived disappearance of a salient target when surrounded by a moving mask. Much research has focused on the role of target characteristics on perceived disappearance by a coherently moving mask. However, we asked a different question: mainly, are there certain characteristics about the mask that can impact disappearance? To address this, we behaviorally tested whether MIB is enhanced or reduced by the property of common fate. In experiments 1, 2, and 3, we systematically manipulated the motion coherence of the mask and measured the amount of target disappearance. Results showed that, as mask coherence increased, perceived target disappearance decreased. This pattern was unaffected by the lifetime of the moving dots, the dot density of the motion stimulus, or the target eccentricity. In experiment 4, we investigated whether the number of motion directions contained in an incoherent mask could account for our findings. Using masks containing 1, 3, and 5 motion directions, we found that disappearance did not increase proportionally to the number of motion directions. We discuss our findings in line with current proposed mechanisms of MIB.     

Perceptual organization of moving stimuli modulates the flash-lag effect

When a visual stimulus is flashed at a given location the moment a second moving stimulus arrives at the same location, observers report the flashed stimulus as spatially lagging behind the moving stimulus (the flash-lag effect). The authors investigated whether the global configuration (perceptual organization) of the moving stimulus influences the magnitude of the flash-lag effect. The results indicate that a flash presented near the leading portion of a moving stimulus lags significantly more than a flash presented near the trailing portion. This result also holds for objects consisting of several elements that group to form a unitary percept of an object in motion. The present study demonstrates a novel interaction between the global configuration of moving objects and the representation of their spatial position and may provide a new and useful tool for the study of perceptual organization.     

On the depth reversibility of point-light actions

We investigate the occurrence of perspective reversals for a depth-ambiguous point-light figure. In addition, we exploit the phenomenon of reversibility to search for stimulus features relevant in the process of depth assignment. Experiment 1 shows that perceptual switches indeed occur during prolonged viewing, although the switches occur infrequently. The reversibility is confirmed in Experiment 2, in which the perceptual ambiguity of the point-light action is manipulated as well as observers’ intention to perceive a particular alternative. In addition, the pattern of eye movements reveals local stimulus features specifically associated with the perception of the different alternatives. In Experiment 3, the importance of these features as determining factors of the initial interpretation is investigated by manipulating the location of the first fixation on the stimulus. Implications for a better understanding of biological motion perception are discussed.     

How do object reference frames and motion vector decomposition emerge in laminar cortical circuits?

How do spatially disjoint and ambiguous local motion signals in multiple directions generate coherent and unambiguous representations of object motion? Various motion percepts, starting with those of Duncker (Induced motion, 1929/1938) and Johansson (Configurations in event perception, 1950), obey a rule of vector decomposition, in which global motion appears to be subtracted from the true motion path of localized stimulus components, so that objects and their parts are seen as moving relative to a common reference frame. A neural model predicts how vector decomposition results from multiple-scale and multiple-depth interactions within and between the form- and motion-processing streams in V1–V2 and V1–MST, which include form grouping, form-to-motion capture, figure–ground separation, and object motion capture mechanisms. Particular advantages of the model are that these mechanisms solve the aperture problem, group spatially disjoint moving objects via illusory contours, capture object motion direction signals on real and illusory contours, and use interdepth directional inhibition to cause a vector decomposition, whereby the motion directions of a moving frame at a nearer depth suppress those directions at a farther depth, and thereby cause a peak shift in the perceived directions of object parts moving with respect to the frame.     

Coherence determines speed discrimination

The visual system must determine which elements in a scene to regard as parts of a single object and which to regard as different objects. We can create stimuli that are ambiguous, ie consistent with more than one interpretation, and ask in what situations the stimulus elements are interpreted as part of a single object and when they are interpreted as multiple objects. The ambiguous stimuli in this study were moving plaid patterns--the sum of two drifting gratings with different orientations. Observers may see a rigid coherent plaid object moving in one direction, or may see two gratings moving in different directions sliding over one another. When the gratings have similar contrasts they appear to cohere and only the plaid speed is perceptually available; when the gratings have different contrasts they appear to slide and only the speeds of the gratings are perceived. Coherence thus determines what speed information is passed to higher stages of motion processing. A two-stage model of plaid motion perception is presented which agrees with the model proposed by Adelson and Movshon and extends it, detailing the relationship between coherence and speed discrimination.     

Multiplicative effects of intention on the perception of bistable apparent motion

When viewing ambiguous displays, observers can, via intentional efforts, affect which perceptual interpretation they perceive. Specifically, observers can increase the probability of seeing the desired percept. Little is known, however, about how intentional efforts interact with sensory inputs in exerting their effects on perception. In two experiments, the current study explored the possibility that intentional efforts might operate by multiplicatively enhancing the stimulus-based activation of the desired perceptual representation. Such a possibility is suggested by recent neurophysiological research on attention. In support of this idea, when we presented bistable apparent motion displays under stimulus conditions differentially favoring one motion percept over the other, observers' intentional efforts to see a particular motion were generally more effective under conditions in which stimulus factors favored the intended motion percept.     

The bar-cross-ellipse illusion: alternating percepts of rigid and nonrigid motion based on contour ownership and trackable feature assignment

We present a new multistable stimulus generated by continuously rotating an ellipse behind four fixed occluders. Despite the stimulus remaining constant, observers can alternate between one of four percepts: (1) a continuously morphing cross; (2) two independent perpendicular bars oscillating in depth; (3) a rigidly rotating ellipse observed behind the occluders; (4) a fixed cross observed through a continuously rotating, elliptical aperture. Interestingly, the initial percept naive observers tend to see is percept 1, which is the only nonrigid motion percept. This appears to be a violation of the hypothesized 'rigidity heuristic' in which rigid motion percepts tend to be perceived over retinally equivalent nonrigid ones. Here, we describe the relationships between each of the percepts and the assignment of contour ownership and figure/ground segmentation.     

Lateral differences in visual inspection time? The role of apparent motion cues

There are a number of reports of a left hemisphere advantage for visual inspection time, but some investigators employing slightly different methodologies have failed to replicate the effect. The present experiment was an attempt to identify one of the factors that could have lead to these discrepant findings: The role of apparent motion cues. In Experiment 1, a lateralized version of the inspection time task was administered via a computer monitor wherein the pi stimulus was masked with a figure vulnerable to apparent motion cues. With this mask, a strong left hemisphere advantage was observed. In Experiments 2 and 3, the test was administered on a tachistoscope or computer monitor, but in both cases the stimulus was masked with a pattern "forest" mask. Under these conditions, there was no lateral difference. This result implies that the left hemisphere advantage for inspection time relies on apparent motion cues.