The effect of instructions on the apparent reversal of rotary motion in depth

This study concerns experimental investigation of the effect of instructions on the apparent reversal of rotary motion in depth. It was found that subjects instructed to report apparent reversals of an elliptical shape signalled more reversals than subjects who were instructed to report the non-occurrence of reversals. This difference increased over four trials. When the stimulus object was a trapezium window instructions to report reversals led to a higher rate of reversals than did instructions to report non-occurrence, but this difference did not increase significantly over trials.     

The effect of reduced spatial cues on the learning of successive visual reversals

The performance of rats over 12 brightness discrimination reversals was studied under two experimental conditions. Under one condition all visual cues external to the apparatus were eliminated so that only the relative positions of the discriminanda could serve as a visual cue to spatial position. Under the other condition all visual cues to position were eliminated. Under the former condition performance deteriorated with successive reversals but under the latter condition performance improved. Implications of these results for theories of successive reversal improvement were discussed and two possible explanations were suggested.     

Effects of visual-field inversions on the reverse-perspective illusion

The 'reverse-perspective' illusion entails the apparent motion of a stationary scene painted in relief and containing misleading depth cues. We have found that, using prism goggles to induce horizontal or vertical visual-field reversals, the illusory motion is greatly reduced or eliminated in the direction for which the goggles reverse the visual field. We argue that the illusion is a consequence of the observer's inability to reconcile changes in visual information due to body movement with implicit knowledge concerning anticipated changes. As such, the reverse-perspective illusion may prove to be useful in the study of the integration of linear perspective and motion parallax information.     

Reversal learning of object and positional discriminations by mink, ferrets and skunks

Mink, ferrets and skunks were tested on successive reversals of two-choice object or positional discriminations in a modified Wisconsin General Training Apparatus. All species showed considerable improvement in performance after considerable training and some subjects exhibited one-trial reversal learning. Mink and ferrets persistently made more errors when position cues were relevant than when object cues were relevant; the reverse was true of skunks.     

Independent perceptual reversals for simultaneously presented ambiguous figures

In two successive experiments using the divided visual field paradigm with vertical or horizontal division, two ambiguous figures, the Rubin’s vase-face or the Necker cube, were projected to the right and left or to the upper and lower visual hemifields of 108 healthy volunteers. Stimulation time was 120 s. The main hypotheses were (a) that different percepts of the same ambiguous figure may be simultaneously experienced in the two hemifields and (b) that the type (vertical vs. horizontal) of visual field division influences the reversal frequency and the temporal interdependence of the percepts.Results from the first experiment showed that the temporal interdependence of reversals was very low for both ambiguous figures, suggesting that during part of the stimulation time the subjects could experience different percepts of the same figure (e.g. a vase in the right and face profiles in the left visual hemifields). The second experiment showed that this perceptual dissociation occurred on average during one third of the stimulation time. In both experiments the type of visual field division did not influence either frequency or temporal interdependence of the reversals. When one single ambiguous figure was presented in the centre of the screen, the number of reversals was approximately the sum of the reversals observed with two figures presented simultaneously each in one hemifield.     

Seven-month-olds detect ordinal numerical relationships within temporal sequences

Previous evidence has shown that 11-month-olds represent ordinal relations between purely numerical values, whereas younger infants require a confluence of numerical and non-numerical cues. In this study, we show that when multiple featural cues (i.e., color and shape) are provided, 7-month-olds detect reversals in the ordinal direction of numerical sequences relying solely on number when non-numerical quantitative cues are controlled. These results provide evidence for the influence of featural information and multiple cue integration on infants’ proneness to detect ordinal numerical information.     

Specificity effects in training and transfer of speeded responses

In 3 experiments, participants, on signal, moved a cursor from a central position to 1 of 8 numerically labeled locations on the circumference of a clock face. Movements were controlled by a mouse in 1 of 4 conditions: vertical reversal, horizontal reversal, combined reversals, or normal (i.e., no reversals). Participants were trained in 1, 2, or 3 of these conditions and were tested 1 week later with either the same or a different condition. There were improvements across training and perfect retention across the delay. There was little or no transfer, however, even when training involved combined reversals or multiple conditions. These results illustrate severe specificity of training and are interpreted in terms of acquired inhibition of normal responses.     

Audiovisual links in exogenous covert spatial orienting

Subjects judged the elevation (up vs. down, regardless of laterality) of peripheral auditory or visual targets, following uninformative cues on either side with an intermediate elevation. Judgments were better for targets in either modality when preceded by an uninformative auditory cue on the side of the target. Experiment 2 ruled out nonattentional accounts for these spatial cuing effects. Experiment 3 found that visual cues affected elevation judgments for visual but not auditory targets. Experiment 4 confirmed that the effect on visual targets was attentional. In Experiment 5, visual cues produced spatial cuing when targets were always auditory, but saccades toward the cue may have been responsible. No such visual-to-auditory cuing effects were found in Experiment 6 when saccades were prevented, though they were present when eye movements were not monitored. These results suggest a one-way cross-modal dependence in exogenous covert orienting whereby audition influences vision, but not vice versa. Possible reasons for this asymmetry are discussed in terms of the representation of space within the brain.     

The misperception of rotary motion

Two principles for predicting the relative frequency of illusory reversals of rotating plane objects were derived and tested empirically. Ten objects, variously’ combining valid and confounding depth cues, were used. Predictions based on the principles were confirmed in every case. The results are offered as an improved explanation of the Ames trapezoid illusion and other illusions of rotary motion.     

Influence of the initial projection of the centre of gravity on posturo-kinetic coordination in humans. Application from a horizontal quadrupedal stance during voluntary limb raising

The purpose of the study is to investigate the influence of initial projection of the centre of gravity (CG) on the spatial and temporal organization of the dynamic phenomena accompanying a voluntary movement in humans. From a horizontal quadrupedal stance, ten normal subjects were instructed to raise the right forelimb towards a support target in self paced velocity conditions. Three experimental conditions were tested for which the initial CG projection was either within (C1), at the limits of (C2) or outside the supporting triangle (C3). The results showed that vertical force variations on the four supports always preceded the first vertical displacement of the right wrist (onset of the movement). From C1 to C3, the duration of these anticipatory dynamic phenomena increased enabling an adjustment of the CG position such that equilibrium constraints were fulfilled. For all conditions, the acceleration peak of the CG occurred prior to the onset of movement and from C1 to C3, its magnitude increased in a single direction of the horizontal plane. For each condition, the load transfer was directed to the left forelimb and the right hindlimb (diagonal strategy) and reached a maximal value at the time of lift-off. With respect to this moment, the onset of the movement occurred increasingly early from C1 to C3. These results suggest that contribution of peripheral cues to postural control is more important, when the requirements of horizontal CG displacement increase.     

Implied body action directs spatial attention

Research confirms that the body influences perception, but little is known about the embodiment of attention. We investigated whether the implied actions of others direct spatial attention, using a lateralized covert-orienting task with nonpredictive central cues depicting static, right/left-facing bodies poised in midaction. Validity effects (decreased response times for validly compared with invalidly cued trials) indicated orienting in the direction of the implied action. In Experiment 1, we compared action (running, throwing) with nonaction (standing) cues. Only the action cues produced validity effects, suggesting that implied action directs attention. The action cues produced faster responses overall, suggesting that action cues prime motor responses. In Experiment 2, we determined whether action cues shifted attention in a specific direction rather than to a general side of space: Two cues had similar action speed and motor effort but differed in implied direction (jumping, vertical; throwing, horizontal). Validity effects were found only for the throw cues for which the implied motion direction was consistent with lateralized target locations. In Experiment 3, we compared block-like stimuli to the throwing action stimuli to examine whether lower level perceptual information could account for the attention effects alone. Validity effects were found only for the human-action stimuli. Overall, the results suggest that predictive simulations of action shift attention in action-consistent directions.     

Attentional shift by eye gaze requires joint attention: Eye gaze cues are unique to shift attention1

Researchers have demonstrated that attentional shift triggered by gaze direction is reflexive. However, here we show that attentional shift by gaze direction was not always reflexive, but could be modulated by another's perspective. In Experiment 1, a schematic face's line of sight to a peripheral target was obstructed by a vertical barrier located between the face and the target under two conditions. However, the line of sight of the face was clear under another two conditions, in which the barrier was located behind the line of sight by utilizing a depth cue. The gaze cue shifted attention only when the line of sight was not blocked (i.e. joint attention was attained). The arrow cue did not shift attention regardless of the obstruction conditions in Experiment 2. These results suggest that attentional shift by gaze cues, but not arrow cues, involve a higher social cognitive process such as interpretation of the gaze.     

Vertical and bisection bias in active touch

We investigated the conditions that underlie the vertical and bisection illusion in touch, in order to understand the basis of their similarity to visual illusions, and the means of reducing the biases in length perception by active touch. Movement, speed, and spatial reference cues were tested. Movements in scanning L-shapes in ipsilateral and contralateral (across the body midline) table-top space produced significant underestimation of the vertical line with the right hand, but not with the left hand. Right-handed scanning of L-shapes showed no significant bias when the vertical line in the figure was aligned to the body midline, suggesting that spatial cues were involved. The vertical line was overestimated in inverted T-shapes, but underestimated in rotated T-shapes, implicating line bisection. Holding scanning latencies constant reduced the vertical error for inverted T-shapes, but could not explain the bisection bias. Sectioning biases were predicted by the location of junctions on sectioned lines, showing that junction points act as misleading anchor cues for movement extents. The illusion was significantly reduced when reference information was added by instructing subjects to relate two-handed scanning of the figure to an external frame and to body-centred cues. It is argued that disparities in spatial reference (anchor) cues for movement extents are involved in vertical and bisection biases in active touch. The hypothesis that length illusions depend on disparities in spatial reference information can also account for the similarity of the tactile to the visual horizontal-vertical illusion.     

An investigation of reversal learning in octopus vulgaris lamarck

Eighteen octopuses were trained by a method of successive discrimination training to discriminate between a vertical and a horizontal rectangle. They were then overtrained for either 20 or 60 trials, after which they learnt the reverse discrimination. At the beginning of each reversal they were given 20 trials pretraining on the new positive stimulus. The subjects completed from two to nine reversals.

It was found that the amount of overtraining had no effect on the rate of learning the subsequent reversal. The first four reversals all took significantly longer to learn than the original problem, but did not differ significantly from one another. However, examination of the raw data suggests that later reversals do take longer to learn. The performance when learnt (i.e. on the first day of overtraining) was as good after reversal learning as after the learning of the original problem.

The results do not show definite signs that could be interpreted as an exhaustion of a limited supply of neurones available for learning.     

Flexible cue use in food-caching birds

An animal’s memory may be limited in capacity, which may result in competition among available memory cues. If such competition exists, natural selection may favor prioritization of different memory cues based on cue reliability and on associated differences in the environment and life history. Food-caching birds store numerous food items and appear to rely on memory to retrieve caches. Previous studies suggested that caching species should always prioritize spatial cues over non-spatial cues when both are available, because non-spatial cues may be unreliable in a changing environment; however, it remains unclear whether non-spatial cues should always be ignored when spatial cues are available. We tested whether mountain chickadees (Poecile gambeli), a food-caching species, prioritize memory for spatial cues over color cues when relocating previously found food in an associative learning task. In training trials, birds were exposed to food in a feeder where both spatial location and color were associated. During subsequent unrewarded test trials, color was dissociated from spatial location. Chickadees showed a significant pattern of inspecting feeders associated with correct color first, prior to visiting correct spatial locations. Our findings argue against the hypothesis that the memory of spatial cues should always take priority over any non-spatial cues, including color cues, in food-caching species, because in our experiment mountain chickadees chose color over spatial cues. Our results thus suggest that caching species may be more flexible in cue use than previously thought, possibly dependent upon the environment and complexity of available cues.     

The perception of visually presented yaw and pitch turns: assessing the contribution of motion, static, and cognitive cues

Terrestrial gravity restricts human locomotion to surfaces in which turns involve rotationsaround the body axis. Because observers are usually upright, one might expect the effects of gravity to induce differences in the processing of vertical versus horizontal turns. Subjects observed visual scenes of bending tunnels, either statically or dynamically, as if they were moving passively through the visual scene and were then asked to reproduce the turn deviation of the tunnel with a trackball. In order to disentangle inertia-related (earth-centered) from vision-related (body-centered) factors, the subjects were either upright or lying on their right side during the observations. Furthermore, the availability of continuous optic flow, geometrical cues, and eye movement were manipulated in three experiments. The results allowed us to characterize the factors' contributions as follows. Forward turns (pitch down) with all cues were largely overestimated, as compared with backward turns (pitch up). First, eye movements known to be irregular for vertical stimulation were largely responsible for this asymmetry. Second, geometry-based estimations are, to some extent, asymmetrical. Third, a cognitive effect corresponding to the evaluation of navigability for upward and downward turns was found (i.e.,top-down influences, such as the fear of falling often reported), which tended to increase the estimation of turns in the direction of gravity.     

On the disruption of visual memory: Interference produced by visual report cues

Report of single letters from centrally-fixated, seven-letter, target rows was probed by either auditory or visual cues. The target rows were presented for 100 ms, and the report cues were single digits which indicated the spatial location of a letter. In three separate experiments, report was always better with the auditory cues. The advantage for the auditory cues was maintained both when target rows were masked by a patterned stimulus and when the auditory cues were presented 500 ms later than comparable visual cues. The results indicate that visual cues produce modality-specific interference which operates at a level of processing beyond iconic representation.     

On the Role of Vertical Texture Cues in Height Perception

When people judge height from the top looking down they tend to overestimate vertical distance. Initial findings suggest that this perceptual bias may be in part due to the experienced fear of falling. However, previous studies did not control for potentially relevant optical invariants, especially vertical texture gradient cues, that may inform such perceptual judgments. In this study, we examined to what degree texture gradient cues may account for the perceptual bias in height perception. To this end, in 2 different conditions in which vertical texture gradient cues were either present or absent, participants provided distance and size judgments from an elevated position (5.68 m) and from the ground. Results revealed a systematic overestimation of vertical extent and object size when judged from a height. Yet, the absence or presence of texture gradient cues did not differentially influence these judgments. Finally, although fear levels were reported to be larger at the elevated position than on the ground, fear levels did not correlate with the perceptual bias, thereby demanding further research into the mechanisms underlying the perceptual bias in height perception.     

Sensitivity of 5- and 7-month-old infants to pictorial depth information

An Ames (1951, Psychological Monographs, 65(1, Whole No. 324)) static trapezoidal window, under monocular view, was used to test young infants' responsiveness to pictorial depth. When adults view this display monocularly with the smaller side of the window rotated toward them, they report that the orientation of the display becomes ambiguous: When the head is moved, the window may appear to be in the fronto-parallel plane or either side may appear closer. The 7-month-olds we tested appeared to experience a similar ambiguity; they reached to the near side of the rotated trapezoidal window with significantly less consistency or directedness than infants in a control group tested with a rotated object that lacked pictorial depth information. When 5-month-olds were tested, however, they reached with equal consistency to the closer side of the trapezoidal window and of the control display, apparently uninfluenced by the pictorial depth information available in the trapezoidal window. Thus, sensitivity to the pictorial information for depth that is present in the trapezoidal window appears to develop after the age of 22 weeks.     

Exploring specificity of speeded aiming movements: Examining different measures of transfer

Participants were trained and tested to move a mouse cursor from a start position to targets on a circular display in a perceptual-motor reversal condition, with horizontal, but not vertical, reversals. During training, some participants (experimental) moved to two targets either along a single diagonal axis (D1) or along both axes (D2). For D2, return movements from the targets were in the same direction as instructed movements to unpracticed targets. Others (control) trained on all targets. Testing always involved all targets. At test, movement times (to reach the target after leaving the start position) were shorter on trained than on untrained targets, especially for the D1 condition, documenting training specificity. However, movement times in the experimental conditions to new targets during testing were shorter than those in the control condition during training, documenting transfer of learning, with more transfer for D2 than for D1. Initiation times (to leave the start position after target onset) showed no transfer. The results provide evidence that specificity and transfer are not mutually exclusive and depend on the measure used to assess performance.