Spatial interval discrimination in the presence of flanking lines

Spatial interval discrimination was studied in the absence or presence of distractors. In the latter case, two flanking lines surrounded two vertical lines delimiting the spatial interval. Using a temporal 2AFC technique with a method of constant stimuli we measured the accuracy of performance (discrimination thresholds) and biases (points of subjective equality) depending on the separations between the target and the flanking lines. For separations less than or comparable to the size of the spatial interval we found both a reduction of precision and the increase of perceived sizes of the spatial intervals: the discrimination thresholds were increased, the size of the spatial interval was overestimated. For larger separations, the size of the spatial interval was underestimated, but the precision of performance was not affected by the presence of flanking lines. We discuss the possible mechanisms underlying spatial interval discrimination in the presence of flanking lines.     

Spatio-temporal parameters and the three-dimensionality of apparent motion: evidence for two types of processing

The minimum ISI required for perceiving apparent motion in depth was measured as a function of the 2D separation of stimuli and the physical separation of stimuli in depth. It was found that temporal thresholds increased as a function of the separation of stimuli in depth. This supports the results of previous research indicating that the perceived three-dimensionality of apparent motion in depth increases with ISI. In addition, the rate of threshold increase was significantly greater in displays with short 2D separations of stimuli than in displays with large 2D separations. This robust functional dissociation of thresholds indicates that the short-range system may be involved in the processing of apparent motion in depth in the former case.     

The role of perceived relative position in pointing to objects apparently shifted by depth-contrast

This paper is concerned with the information used in open-loop pointing to visually perceived targets. Stereoscopic stimuli were used to produce illusory relative egocentric distances, which were inconsistent with the angles of vergence required to fuse the targets. One of the stimuli was a rectangle slanted around a vertical axis. Four participants in Experiment 1 reported its slant and pointed to its edges. The slant was hugely underestimated (condition A) unless the rectangle was flanked by other surfaces (condition B). The relative depth of a pair of dots placed in front of the rectangle was also misperceived due to depth-contrast effect. The critical finding is that pointing responses were not based on vergence but were consistent with depth estimates, both for the rectangle and for the dots. Experiment 2 revealed the conditions necessary for pointing to be consistent with perceived relative position. The different target distances were either randomised allowing inter-trial comparisons, or presented only one per session to prevent them. Pointing was similar to estimates only in the randomised condition showing the significance of inter-trial comparisons. It is proposed that participants used the remembered motor command and kinesthetic sensations of a previous movement as a reference, attempting to make the difference between successive movements the same as a visually perceived depth difference between successive targets.     

Effects of stimulus size and spatial organization on pigeons’ conditional same-different discrimination

In two experiments, we explored the effects of varying the size and the spatial organization of the stimuli in multi-item arrays on pigeons’ same-different discrimination behavior. The birds had previously learned to discriminate a simultaneously presented array of 16 identical (Same) visual items from an array of 16 nonidentical (Different) visual items, when the correct choice was conditional on the presence of another cue: the color of the background (Castro et al., in press). In Experiment 1, we trained pigeons with 7-item arrays and then tested them with arrays containing the same item, but in a variety of sizes. In Experiment 2, we tested the birds with the items grouped in novel locations: the top, the bottom, the left, or the right portions of the display area, which generated different vertical and horizontal alignments. Accuracy scores revealed virtually perfect stimulus generalization across various item sizes and spatial organizations. Reaction times revealed that the birds perceived different sizes of a single icon as the same stimulus (Experiment 1) and that the birds processed vertical arrangements faster than horizontal arrangements (Experiment 2). These results suggest that the pigeons noticed both physical and spatial changes in the stimuli (as shown by their reaction times), but that these changes did not disrupt the birds’ discriminating the sameness or differentness of the multi-item arrays (as shown by their accuracy scores).     

Effects of adaptation to apparent movement on recovery of structure from motion.

Past work on the recovery of three-dimensional structure from dynamic two-dimensional images has led to inconsistent conclusions regarding the contributions of the short-range and long-range motion processes. In the present experiments, subjects adapted to displays (either four lines or 50 randomly positioned pixels) whose spatiotemporal parameters were chosen to favor either the short-range or long-range process. Adaptation periods were followed by test displays that simulated the rotation of a four-pixel random object about the vertical gamma-axis. The dependent measure was the angle of rotation between successive frames of the rotation display at which percepts of three-dimensional structure broke down. Both the original data and derived measures based on best-fitting polynomials showed small but consistent effects: Compared to control conditions, adaptation to short-range motion reduced the angle at which percepts of structure broke down; adaptation to long-range motion increased them. It is suggested that both low-level (i.e. short-range) and high-level (long-range) processes contribute to the recovery of structure from motion.     

Evolution of Anoline Lizard Display Behavior

Based on my conceptual framework of anoline display behavior,I am suggesting the following evolutionary trends. Lateral presentationduring display was probably promoted by monocular vision. Alongwith lateral presentation, postures evolved to increase lateraloutline. These postures which magnified body size were probablyof selective advantage within aggressive social contexts sincelarger animals tend to dominate smaller ones through bluff.Body movement evolved along with lateral orientation and size-enhancingpostures. These movements would be most effective if they complementedlateral orientation. Effectors available for such movementswere primarily pre-adapted for vertical motion. The patternsof movement generated were probably simple oscillatory bobbingmovements by the head which were weakly stereotyped, interspecificallysimilar, appearing in many contexts, and having a weakly definedinformation content. Events having selective advantage for speciesrecognition promoted stereotypy of bobbing behavior into species-uniquedisplays; each species had its unique signature display whichserved in a manifold communicatory capacity. The signature displayappeared in assertion, courtship, and challenge contexts. Itsinformation content varied depending upon context and recipientof the display (e.g., male or female). Besides the stereotypedaspects of the display, certain features remained variable withpotential information significance. Core variability (see text)promotes individual recognition and may be the origin of newunique display patterns as sibling species emerge. Display modifiers(see text) are variable display features shared by members ofa population (many being shared interspecifically) that providea graded appearance to display performance; modifiers can indicatelevel of arousal and facilitate interspecific communication.For some species display repertoire size seems to have evolvedfrom a single display (signature display) to repertoires ofmultiple displays; these subsequent displays are generally restrictedto aggressive interactions.     

Frame of reference transformations in motion perception during smooth pursuit eye movements

Smooth pursuit eye movements change the retinal image velocity of objects in the visual field. In order to change from a retinocentric frame of reference into a head-centric one, the visual system has to take the eye movements into account. Studies on motion perception during smooth pursuit eye movements have measured either perceived speed or perceived direction during smooth pursuit to investigate this frame of reference transformation, but never both at the same time. We devised a new velocity matching task, in which participants matched both perceived speed and direction during fixation to that during pursuit. In Experiment 1, the velocity matches were determined for a range of stimulus directions, with the head-centric stimulus speed kept constant. In Experiment 2, the retinal stimulus speed was kept approximately constant, with the same range of stimulus directions. In both experiments, the velocity matches for all directions were shifted against the pursuit direction, suggesting an incomplete transformation of the frame of reference. The degree of compensation was approximately constant across stimulus direction. We fitted the classical linear model, the model of Turano and Massof (2001) and that of Freeman (2001) to the velocity matches. The model of Turano and Massof fitted the velocity matches best, but the differences between de model fits were quite small. Evaluation of the models and comparison to a few alternatives suggests that further specification of the potential effect of retinal image characteristics on the eye movement signal is needed.     

Spatial Attention Is Attracted in a Sustained Fashion toward Singular Points in the Optic Flow

While a single approaching object is known to attract spatial attention, it is unknown how attention is directed when the background looms towards the observer as s/he moves forward in a quasi-stationary environment. In Experiment 1, we used a cued speeded discrimination task to quantify where and how spatial attention is directed towards the target superimposed onto a cloud of moving dots. We found that when the motion was expansive, attention was attracted towards the singular point of the optic flow (the focus of expansion, FOE) in a sustained fashion. The effects were less pronounced when the motion was contractive. The more ecologically valid the motion features became (e.g., temporal expansion of each dot, spatial depth structure implied by distribution of the size of the dots), the stronger the attentional effects. Further, the attentional effects were sustained over 1000 ms. Experiment 2 quantified these attentional effects using a change detection paradigm by zooming into or out of photographs of natural scenes. Spatial attention was attracted in a sustained manner such that change detection was facilitated or delayed depending on the location of the FOE only when the motion was expansive. Our results suggest that focal attention is strongly attracted towards singular points that signal the direction of forward ego-motion.     

Asymmetries in oriented-line detection indicate two orthogonal filters in early vision.

Visual detection of a line target differing in orientation from a background of lines may be achieved speedily and effortlessly. Such performance is assumed to occur early in vision and to involve filter mechanisms acting in parallel over the visual field. This study establishes orientational limits on this performance and analytically derives some generic properties of the underlying filters. It was found that, in brief displays, target orientation detection thresholds increased approximately linearly with background orientation, from minima at 0 degree (vertical) and 90 degrees, whereas background orientation detection thresholds decreased approximately linearly with target orientation, from maxima at 0 degree and 90 degrees. Target and background threshold functions were exactly antisymmetric. These data are shown to indicate a model of early line processing dominated by two classes of orientation-sensitive filter with axes close to the vertical and horizontal and orientation-tuning half-widths each of approximately 30 degrees at half-height.     

Stereoscopic and contrast-defined motion in human vision.

There is considerable evidence for the existence of a specialized mechanism in human vision for detecting moving contrast modulations and some evidence for a mechanism for detecting moving stereoscopic depth modulations. It is unclear whether a single second-order motion mechanism detects both types of stimulus or whether they are detected separately. We show that sensitivity to stereo-defined motion resembles that to contrast-defined motion in two important ways. First, when a missing-fundamental disparity waveform is moved in steps of 0.25 cycles, its perceived direction tends to reverse. This is a property of both luminance-defined and contrast-defined motion and is consistent with independent detection of motion at different spatial scales. Second, thresholds for detecting the direction of a smoothly drifting sinusoidal disparity modulation are much higher than those for detecting its orientation. This is a property of contrast-modulated gratings but not luminance-modulated gratings, for which the two thresholds are normally identical. The results suggest that stereo-defined and contrast-defined motion stimuli are detected either by a common mechanism or by separate mechanisms sharing a common principle of operation.     

Prediction of a moving target's position in fast goal-directed action

 Subjects made fast goal-directed arm movements towards moving targets. In some cases, the perceived direction of target motion was manipulated by moving the background. By comparing the trajectories towards moving targets with those towards static targets, we determined the position towards which subjects were aiming at movement onset. We showed that this position was an extrapolation in the target’s perceived direction from its position at that moment using its perceived direction of motion. If subjects were to continue to extrapolate in the perceived direction of target motion from the position at which they perceive the target at each instant, the error would decrease during the movements. By analysing the differences between subjects’ arm movements towards targets moving in different (apparent) directions with a linear second-order model, we show that the reduction in the error that this predicts is not enough to explain how subjects compensate for their initial misjudgements. Received: 10 February 1995/Accepted in revised form: 30 May 1995     

Properties of individual movement detectors as derived from behavioural experiments on the visual system of the fly

The performance of the fly's movement detection system is analysed using the visually induced yaw torque generated during tethered flight as a behavioural indicator. In earlier studies usually large parts of the visual field were exposed to the movement stimuli; the fly's response, therefore, represented the spatially pooled output signals of a large number of local movement detectors. Here we examined the responses of individual movement detectors. The stimulus pattern was presented to the fly via small vertical slits, thus, nearly avoiding spatial integration of local movement information along the horizontal axis of the eye. The stimulus consisted of a vertically oriented sine-wave grating which was moved with a constant velocity either clockwise or counterclockwise. In agreement with the theory of movement detectors of the correlation type, the time-course of the detector signal is modulated with the spatial phase of the stimulus pattern. It can even assume negative values for some time during the response cycle and thus signal the wrong direction of motion. By spatially integrating the response over sufficiently large arrays of movement detectors these response modulations disappear. Finally, one obtains a signal of the movement detection system which is constant while the pattern moves in one direction and only changes its sign when the pattern reverses its direction of motion. Spatial integration thus represents a simple means to obtain a meaningful representations of motion information.     

Effects of Haptic Information on the Perception of Dynamic 3-D Movement

This study examined effects of hand movement on visual perception of 3-D movement. I used an apparatus in which a cursor position in a simulated 3-D space and the position of a stylus on a haptic device could coincide using a mirror. In three experiments, participants touched the center of a rectangle in the visual display with the stylus of the force-feedback device. Then the rectangle''s surface stereoscopically either protruded toward a participant or indented away from the participant. Simultaneously, the stylus either pushed back participant''s hand, pulled away, or remained static. Visual and haptic information were independently manipulated. Participants judged whether the rectangle visually protruded or dented. Results showed that when the hand was pulled away, subjects were biased to perceive rectangles indented; however, when the hand was pushed back, no effect of haptic information was observed (Experiment 1). This effect persisted even when the cursor position was spatially separated from the hand position (Experiment 2). But, when participants touched an object different from the visual stimulus, this effect disappeared (Experiment 3). These results suggest that the visual system tried to integrate the dynamic visual and haptic information when they coincided cognitively, and the effect of haptic information on visually perceived depth was direction-dependent.     

Human Vection Perception Using Inertial Nulling and Certainty Estimation: The Effect of Migraine History

Vection is an illusory perception of self-motion that can occur when visual motion fills the majority of the visual field. This study examines the effect of the duration of visual field movement (VFM) on the perceived strength of self-motion using an inertial nulling (IN) and a magnitude estimation technique based on the certainty that motion occurred (certainty estimation, CE). These techniques were then used to investigate the association between migraine diagnosis and the strength of perceived vection. Visual star-field stimuli consistent with either looming or receding motion were presented for 1, 4, 8 or 16s. Subjects reported the perceived direction of self-motion during the final 1s of the stimulus. For the IN method, an inertial nulling motion was delivered during this final 1s of the visual stimulus, and subjects reported the direction of perceived self-motion during this final second. The magnitude of inertial motion was varied adaptively to determine the point of subjective equality (PSE) at which forward or backward responses were equally likely. For the CE trials the same range of VFM was used but without inertial motion and subjects rated their certainty of motion on a scale of 0–100. PSE determined with the IN technique depended on direction and duration of visual motion and the CE technique showed greater certainty of perceived vection with longer VFM duration. A strong correlation between CE and IN techniques was present for the 8s stimulus. There was appreciable between-subject variation in both CE and IN techniques and migraine was associated with significantly increased perception of self-motion by CE and IN at 8 and 16s. Together, these results suggest that vection may be measured by both CE and IN techniques with good correlation. The results also suggest that susceptibility to vection may be higher in subjects with a history of migraine.     

A system of insect neurons sensitive to horizontal and vertical image motion connects the medulla and midbrain

Summary The response properties and gross morphologies of neurons that connect the medulla and midbrain in the butterfly Papilio aegeus are described. The neurons presented give direction-selective responses, i.e. they are excited by motion in the preferred direction and the background activity of the cells is inhibited by motion in the opposite, null, direction. The neurons are either maximally sensitive to horizontal motion or to slightly off-axis vertical upward or vertical downward motion, when tested in the frontal visual field. The responses of the cells are dependent on the contrast frequency of the stimulus with peak values at 5–10 Hz. The receptive fields of the medulla neurons are large and are most sensitive in the frontal visual field. Examination of the local and global properties of the receptive fields of the medulla neurons indicates that (1) they are fed by local elementary motion-detectors consistent with the correlation model and (2) there is a non-linear spatial integration mechanism in operation.     

A psychophysical and computational analysis of intensity–based stereo

We describe two psychophysical experiments testing predictions of the square difference mechanism we have previously proposed for intensity–based stereo. Experiment 1 assesses the relative contributions of disparity and contrast to intensity–based stereo by measuring detection thresholds. The product of disparity and contrast at threshold is shown to be constant. In experiment 2, we measure quantitatively the global depth position perceived in stereograms of curved, smoothly shaded surfaces. The results show that disparity averaging over the surface involves a contrast-dependent weighting function. The results from both experiments are consistent with predictions derived from the square difference mechanism. The relation of this mechanism to feature correspondence stereopsis and shape–from–shading is discussed and a general framework for assessing the modularity of stereopsis is presented. Received: 9 June 1995 / Accepted in revised form: 3 June 1996     

Human Discrimination of the Angular Velocity of the Vertical Movement of an Acoustic Image in Opposite Directions

The discrimination of the angular velocity of ventrodorsal and dorsoventral movement of an acoustic image was studied in nine test subjects. The experiments were performed using an apparent movement produced by consecutive activation of loudspeakers located along an arc in the vertical plane. The differential thresholds were measured by the minimum increment method. As the velocity of an acoustic image movement in opposite directions increased, the values of its mean absolute differential thresholds increased monotonically. Regression lines plotted by linear approximation of these values did not differ significantly.     

Responses of tectal neurons to contrasting stimuli: an electrophysiological study in the barn owl

The saliency of visual objects is based on the center to background contrast. Particularly objects differing in one feature from the background may be perceived as more salient. It is not clear to what extent this so called "pop-out" effect observed in humans and primates governs saliency perception in non-primates as well. In this study we searched for neural-correlates of pop-out perception in neurons located in the optic tectum of the barn owl. We measured the responses of tectal neurons to stimuli appearing within the visual receptive field, embedded in a large array of additional stimuli (the background). Responses were compared between contrasting and uniform conditions. In a contrasting condition the center was different from the background while in the uniform condition it was identical to the background. Most tectal neurons responded better to stimuli in the contrsating condition compared to the uniform condition when the contrast between center and background was the direction of motion but not when it was the orientation of a bar. Tectal neurons also preferred contrasting over uniform stimuli when the center was looming and the background receding but not when the center was receding and the background looming. Therefore, our results do not support the hypothesis that tectal neurons are sensitive to pop-out per-se. The specific sensitivity to the motion contrasting stimulus is consistent with the idea that object motion and not large field motion (e.g., self-induced motion) is coded in the neural responses of tectal neurons.     

The Effect of Furnishing on Perceived Spatial Dimensions and Spaciousness of Interior Space

Despite the ubiquity of interior space design, there is virtually no scientific research on the influence of furnishing on the perception of interior space. We conducted two experiments in which observers were asked to estimate the spatial dimensions (size of the room dimensions in meters and centimeters) and to judge subjective spaciousness of various rooms. Experiment 1 used true-to-scale model rooms with a square surface area. Furnishing affected both the perceived height and the spaciousness judgments. The furnished room was perceived as higher but less spacious. In Experiment 2, rooms with different square surface areas and constant physical height were presented in virtual reality. Furnishing affected neither the perceived spatial dimensions nor the perceived spaciousness. Possible reasons for this discrepancy, such as the influence of the presentation medium, are discussed. Moreover, our results suggest a compression of perceived height and depth with decreasing surface area of the room.     

Adaptation effects in the analyzer of movement direction

A prolonged observation of a point-like stimulus moving in a given direction influences the perception of movement direction of subsequent stimuli. The prolonged observation of the same stimulus results in a subjective drift of the perceived movement towards horizontal or vertical direction depending on which of these directions is nearer to the stimulus trajectory. If, however, the stimulus moves in vertical, diagonal and horizontal directions its perception does not change under prolonged observation.