Visual grouping by motion precedes the relative localization between moving and flashed stimuli

A flashed stimulus is perceived as spatially lagging behind a moving stimulus when they are spatially aligned. When several elements are perceptually grouped into a unitary moving object, a flash presented at the leading edge of the moving stimulus suffers a larger spatial lag than a flash presented at the trailing edge (K. Watanabe. R. Nijhawan. B. Khurana, & S. Shimojo. 2001). By manipulation of the flash onset relative to the motion onset, the present study investigated the order of perceptual operations of visual motion grouping and relative visual localization. It was found that the asymmetric mislocalization was observed irrespective of physical and/or perceptual temporal order between the motion and flash onsets. Thus, grouping by motion must be completed to define the leading-trailing relation in a moving object before the visual system explicitly represents the relative positions of moving and flashed stimuli.     

Attentional set for axis of symmetry in symmetry-defined visual search

Olivers and van der Helm (1998) showed that symmetry-defined visual search (for both symmetry and asymmetry) requires selective spatial attention. We hypothesize that an attentional set for the orientation of a symmetry axis also is involved in symmetry-defined visual search. We conducted three symmetry-defined visual search experiments with manipulations of the axis of symmetry orientations, and performance was better when the axis orientations within the search array were uniform, rather than a mixture of two orientations, and the attentional set for the axis orientation could be kept. In addition, search performance when the target was defined by the presence of symmetry was equivalent to that when the target was defined by a difference of symmetry axis orientation. These results suggest that attentional set for axis orientation plays a fundamental role in symmetry-defined visual search.     

Object-based anisotropies in the flash-lag effect

The relative visual position of a briefly flashed stimulus is systematically modified in the presence of motion signals. We investigated the two-dimensional distortion of the positional representation of a flash relative to a moving stimulus. Analysis of the spatial pattern of mislocalization revealed that the perceived position of a flash was not uniformly displaced, but instead shifted toward a single point of convergence that followed the moving object from behind at a fixed distance. Although the absolute magnitude of mislocalization increased with motion speed, the convergence point remained unaffected. The motion modified the perceived position of a flash, but had little influence on the perceived shape of a spatially extended flash stimulus. These results demonstrate that motion anisotropically distorts positional representation after the shapes of objects are represented. Furthermore, the results imply that the flash-lag effect may be considered a special case of two-dimensional anisotropic distortion.     

Asymmetric mislocalization of a visual flash ahead of and behind a moving objectt

When subjects localize a flash relative to another stationary stimulus, the flash appears displaced in the direction of nearby motion signals (position capture; Whitney and Cavanagh, 2000 Nature Neuroscience 3 954-959). Our previous study had suggested that the position capture is larger for a flash presented ahead of a moving stimulus than for a flash behind it (Watanabe et al, 2003 Perception 32 545-559). In the present study, I investigated the spatial asymmetry of position capture. Experiment 1 demonstrated that asymmetric position capture occurs primarily in a moving-object-centered coordinate. Experiment 2 showed evidence that the asymmetric position capture operates after individuation of single visual objects. Finally, experiment 3 demonstrated that, when attention was reduced with a dual-task procedure, the asymmetric position capture increased. These results suggest that the spatial asymmetry of position capture occurs without attention but the spatial bias can be reduced by attention. Therefore, the underlying mechanism for the asymmetric spatial bias may be different from attentive tracking (Cavanagh, 1992 Science 257 1563-1565) and mislocalization during smooth pursuit (Brenner et al, 2001 Vision Research 41 2253-2259).     

Perceived standing position after reduction of foot-pressure sensation by cooling the sole

We investigated the influence of the reduction of foot-pressure sensation by cooling the sole of the foot, at 1 degree C for 30 or 40 minutes, on the perception of standing position varied in the anteroposterior direction. The subjects were 16 healthy undergraduates. Firstly, for 4 of the subjects, cooling the sole of the foot decreased sensory information from the mechanoreceptors in the sole, by testing for an increase in the threshold for two-point discrepancy discrimination on the sole of the foot and for the disappearance of postural change with vibration to the sole. Next, the perception of standing position was measured by reproduction of a given standing reference position involving forward or backward leaning under both normal and cooled conditions of the feet. Standing position was varied in relation to the location of the center of foot pressure, defined as distance from the heel in percentage of the length of the foot. The reference positions, representing various locations of the center of foot pressure, were set at 10% increments from 20% to 80% of the length of the foot. With eyes closed, the subject first experienced the reference position and then attempted to reproduce it. The mean location of the center of foot pressure in the quiet standing posture was 45.7%. At the 40%, 50%, and 60% reference positions, those closest to quiet standing, absolute errors of reproduction were significantly larger than at other reference positions in both the normal and the cooled conditions. They were significantly larger in the cooled than in the normal condition. The 50% and 60% reference positions were reproduced significantly further forward in the cooled than in the normal condition. These results may be explained as due to an absence of marked changes in sensory information from both muscular activity and foot pressure when moving to reference positions close to the quiet standing posture.     

Differential effect of distractor timing on localizing versus identifying visual changes

When visual changes are accompanied by visual transients, such as in the case of saccades, eye blinks, and brief flickers, they often go unnoticed; this phenomenon is called change blindness (Rensink, R. A. (2002). Change detection. Annual Review of Psychology 53, 245; Simons, D. J., & Levin, D. T. (1997). Change blindness. Trends in Cognitive Sciences 1, 261). Change blindness occurs even when the position of visual transients does not cover the location of the change (as in the 'mudsplash' paradigm) (O'Regan, J. K., Rensink, R. A., & Clark, J. J. (1999). Nature 398, 34). By using a simplified mudsplash display, the present study investigated whether change blindness depends on (a). the timing of visual transients, and (b). the task that observers perform. Eight Gabor elements with random orientations were presented. One element (target) was rotated 45 degrees clockwise or counterclockwise without a temporal gap. High contrast visual transients, not overlapping with the elements, appeared at various times with respect to the target change. Observers reported where the change was (change localization), or in which direction the target rotated (change identification). Change localization was impaired primarily when the onset of the transient was at or after the change. In contrast, change identification was impaired mainly when the transient preceded the change. These results suggest that change localization and change identification are mediated in part by different mechanisms.     

A Cut-Free Sequent System for the Smallest Interpretability Logic

The idea of interpretability logics arose in Visser [Vis90]. He introduced the logics as extensions of the provability logic GLwith a binary modality . The arithmetic realization of A B in a theory T will be that T plus the realization of B is interpretable in T plus the realization of A (T + A interprets T + B). More precisely, there exists a function f (the relative interpretation) on the formulas of the language of T such that T + B C implies T + A f(C).The interpretability logics were considered in several papers. An arithmetic completeness of the interpretability logic ILM, obtained by adding Montagna's axiom to the smallest interpretability logic IL, was proved in Berarducci [Ber90] and Shavrukov [Sha88] (see also Hájek and Montagna [HM90] and Hájek and Montagna [HM92]). [Vis90] proved that the interpretability logic ILP, an extension of IL, is also complete for another arithmetic interpretation. The completeness with respect to Kripke semantics due to Veltman was, for IL, ILMand ILP, proved in de Jongh and Veltman [JV90]. The fixed point theorem of GLcan be extended to ILand hence ILMand ILP(cf. de Jongh and Visser [JV91]). The unary pendant "T interprets T + A" is much less expressive and was studied in de Rijke [Rij92]. For an overview of interpretability logic, see Visser [Vis97], and Japaridze and de Jongh [JJ98].In this paper, we give a cut-free sequent system for IL. To begin with, we give a cut-free system for the sublogic IL4of IL, whose -free fragment is the modal logic K4. A cut-elimination theorem for ILis proved using the system for IK4and a property of Löb's axiom.     

Retrospective perceptual distortion of position representation does not lead to delayed localization

Previous studies have reported retrospective influences of visual events that occur after target events. In the attentional attraction effect, a position cue presented after a target stimulus distorts the target’s position towards that of the cue. The present study explored the temporal relationship between stimulus presentation and reaction time (RT) in this effect in two experiments. Participants performed a speeded localization task on two vertical lines, the positions of which were to be distorted by an additional attentional cue. No significant difference in RTs was found between the conditions with simultaneous and delayed cues. RTRT was modulated by the perceived (rather than physical) alignment of the lines. In Experiment 2, we manipulated the strength of attentional capture by modulating the color relevance of the cue to the target. Trials with cues producing stronger attentional capture (with cues of a different color from the targets) were found to induce apparently stronger distortion effects. This result favors the notion that the observed repulsion and attraction effects are driven by attentional mechanisms. Overall, the results imply that the attentional shift induced by the cue might occur rapidly and complete before the establishment of conscious location representation of the cue and the target without affecting overall response time.     

Effects of direct and averted gaze on the subsequent saccadic response

The saccadic latency to visual targets is susceptible to the properties of the currently fixated objects. For example, the disappearance of a fixation stimulus prior to presentation of a peripheral target shortens saccadic latencies (the gap effect). In the present study, we investigated the influences of a social signal from a facial fixation stimulus (i.e., gaze direction) on subsequent saccadic responses in the gap paradigm. In Experiment 1, a cartoon face with a direct or averted gaze was used as a fixation stimulus. The pupils of the face were unchanged (overlap), disappeared (gap), or were translated vertically to make or break eye contact (gaze shift). Participants were required to make a saccade toward a target to the left or the right of the fixation stimulus as quickly as possible. The results showed that the gaze direction influenced saccadic latencies only in the gaze shift condition, but not in the gap or overlap condition; the direct-to-averted gaze shift (i.e., breaking eye contact) yielded shorter saccadic latencies than did the averted-to-direct gaze shift (i.e., making eye contact). Further experiments revealed that this effect was eye contact specific (Exp. 2) and that the appearance of an eye gaze immediately before the saccade initiation also influenced the saccadic latency, depending on the gaze direction (Exp. 3). These results suggest that the latency of target-elicited saccades can be modulated not only by physical changes of the fixation stimulus, as has been seen in the conventional gap effect, but also by a social signal from the attended fixation stimulus.