Spatial representation in body coordinates: evidence from errors in remembering positions of visual and auditory targets after active eye, head, and body movements.

Eight participants were presented with auditory or visual targets and then indicated the target's remembered positions relative to their head eight seconds after actively moving their eyes, head or body to pull apart head, retinal, body, and external space reference frames. Remembered target position was indicated by repositioning sounds or lights. Localization errors were found related to head-on-body position but not of eye-in-head or body-in-space for both auditory (0.023 dB/deg in the direction of head displacement) and visual targets (0.068 deg/deg in the direction opposite to head displacement). The results indicate that both auditory and visual localization use head-on-body information, suggesting a common coding into body coordinates--the only conversion that requires this information.     

Position constancy and binocular convergence

The position constancy during head movement of a luminous spot in a dark room depends in part on the convergence state of the eyes. This supports a modified form of the theory that an optical-motion/head-motion comparator contributes to constancy. By incorporating convergence information, the comparator can allow [or the effect of parallax on the optical-motion/body-motion ratio.     

Target distance and adaptation in distance perception in the constancy of visual direction

Hay and Sawyer recently demonstrated that the constancy of visual direction (CVD) also operates for near targets. A luminous spot in the dark, 40 cm from the eyes, was perceived as stationary when S nodded his head. This implies that CVD takes target distance, as well as head rotation, into account as a stationary environment is perceived during head movements. Distance is a variable in CVD because, during a turning or nodding of the head, the eyes become displaced relative to the main target direction, the line between the target and the rotation axis of the head. This displacement of the eyes during head rotation causes an additional change in the target direction, i.e., a total angular change greater than the angle of the head rotation. The extent of this additional angular displacement is greater the nearer the target. We demonstrated that the natural combination of accommodation and convergence can supply the information needed by the nervous system to compensate for this additional target displacement. We also found that wearing glasses that alter the relation between these oculomotor adjustments and target distance produces an adaptation in CVD. An adaptation period of 1.5 h produced a large adaptation effect. This effect was not entirely accounted for by an adaptation in distance perception. Measurements of the alteration between oculomotor cues and registered distance with two kinds of tests for distance perception yielded effects significantly smaller than the effect measured with the CVD test. We concluded that the wearing of the glasses had also produced an adaptation within CVD.     

The whereabouts of visual attention: Involuntary attentional bias toward the default gaze direction

This study proposed and verified a new hypothesis on the relationship between gaze direction and visual attention: attentional bias by default gaze direction based on eye-head coordination. We conducted a target identification task in which visual stimuli appeared briefly to the left and right of a fixation cross. In Experiment 1, the direction of the participant’s head (aligned with the body) was manipulated to the left, front, or right relative to a central fixation point. In Experiment 2, head direction was manipulated to the left, front, or right relative to the body direction. This manipulation was based on results showing that bias of eye position distribution was highly correlated with head direction. In both experiments, accuracy was greater when the target appeared at a position where the eyes would potentially be directed. Consequently, eye–head coordination influences visual attention. That is, attention can be automatically biased toward the location where the eyes tend to be directed.     

Eye-position aftereffects of backward head tilt manifested by illusory visual direction

Three experiments showed posttest-minus-pretest shifts in subjective straight-ahead eye position when subjects read for 3, 6, or 9 min with their heads tilted back 20° from upright. These shifts were significant relative to control conditions in which subjects read with their heads upright. All subjects read with the same straight-ahead eye-in-head position. Variability-reducing procedures were developed to provide better measures over Experiments 1, 2. and 3. Explanations in terms of deliberate compensation, head-position asymmetries, eye-position asymmetries, and progressive error were ruled out. It was hypothesized that the shifts were caused by negative aftereffects of compensation for the doll reflex. The doll reflex rotates the eyes down without central registration. causing an upward illusory shift of visual direction similar to what is caused by wedge prisms. Perceptual-motor adaptation to this shift, i.e., doll adaptation, causes an illusory shift in the opposite direction when the head is returned to upright.     

Effects of head orientation on gaze perception: How positive congruency effects can be reversed

Several past studies have considered how perceived head orientation may be combined with perceived gaze direction in judging where someone else is attending. In three experiments we tested the impact of different sources of information by examining the role of head orientation in gaze-direction judgements when presenting: (a) the whole face; (b) the face with the nose masked; (c) just the eye region, removing all other head-orientation cues apart from some visible part of the nose; or (d) just the eyes, with all parts of the nose masked and no head orientation cues present other than those within the eyes themselves. We also varied time pressure on gaze direction judgements. The results showed that gaze judgements were not solely driven by the eye region. Gaze perception can also be affected by parts of the head and face, but in a manner that depends on the time constraints for gaze direction judgements. While “positive” congruency effects were found with time pressure (i.e., faster left/right judgements of seen gaze when the seen head deviated towards the same side as that gaze), the opposite applied without time pressure.     

Adaptation in the constancy of visual direction tested by measuring the constancy of auditory direction

Modification of the constancy of visual direction was produced by partially adapting Ss to the displacements of the visual field caused by magnifying lenses during 1 h of continuous head turning. The adaptation effects were measured by determining the range of perceived target immobility before and after this adaptation period. A method for measuring the range of apparent immobility of an auditory signal during head movements was developed and employed to test whether a modification of the constancy of visual direction transfers to the constancy of auditory direction. No such transfer was found, and it was concluded that a modification of the constancy of visual direction does not consist in an altered evaluation of kinesthetic cues for head turning. The method and the equipment used in the investigation of the constancy of visual direction are described; knowledge of the previous brief publications on this topic is not needed.     

Effects of head orientation on gaze perception: how positive congruency effects can be reversed

Several past studies have considered how perceived head orientation may be combined with perceived gaze direction in judging where someone else is attending. In three experiments we tested the impact of different sources of information by examining the role of head orientation in gaze-direction judgements when presenting: (a) the whole face; (b) the face with the nose masked; (c) just the eye region, removing all other head-orientation cues apart from some visible part of the nose; or (d) just the eyes, with all parts of the nose masked and no head orientation cues present other than those within the eyes themselves. We also varied time pressure on gaze direction judgements. The results showed that gaze judgements were not solely driven by the eye region. Gaze perception can also be affected by parts of the head and face, but in a manner that depends on the time constraints for gaze direction judgements. While “positive” congruency effects were found with time pressure (i.e., faster left/right judgements of seen gaze when the seen head deviated towards the same side as that gaze), the opposite applied without time pressure.     

ON THE NONVISUAL CUES CONTROLLING THROWlNG MOVEMENTS

M ikkonen , V. & K olehmainen , K. On the nonvisual cues controlling throwing movements. Scand. J. Psychol ., 1968, 9, 169–176.—When position of subject's head is varied (his eyes fixating the target) in dart throwing experiments, systematic errors occur in the throws in the direction in which the head is turned. Subjects trained to hit the target with the head turned to the side, and then allowed to throw with the face towards the target, make errors in the direction opposite to that in which the head was turned during training. The most recently learned relationship between head and hand thus tends to guide the throws. Changes occur primarily in the direction of the throwing movement, the starting position of the throwing hand being relatively stable.     

The interaction of perceived distance with the perceived direction of visual motion during movements of the eyes and the head.

A horizontally moving target was followed by rotation of the eyes alone or by a lateral movement of the head. These movements resulted in the retinal displacement of a vertically moving target from its perceived path, the amplitude of which was determined by the phase and amplitude of the object motion and of the eye or head movements. In two experiments, we tested the prediction from our model of spatial motion (Swanston, Wade, & Day, 1987) that perceived distance interacts with compensation for head movements, but not with compensation for eye movements with respect to a stationary head. In both experiments, when the vertically moving target was seen at a distance different from its physical distance, its perceived path was displaced relative to that seen when there was no error in perceived distance, or when it was pursued by eye movements alone. In a third experiment, simultaneous measurements of eye and head position during lateral head movements showed that errors in fixation were not sufficient to require modification of the retinal paths determined by the geometry of the observation conditions in Experiments 1 and 2.     

The interaction of perceived distance with the perceived direction of visual motion during movements of the eyes and the head

A horizontally moving target was followed by rotation of the eyes alone or by a lateral movement of the head. These movements resulted in the retinal displacement of a vertically moving target from its perceived path, the amplitude of which was determined by the phase and amplitude of the object motion and of the eye or head movements. In two experiments, we tested the prediction from our model of spatial motion (Swanston, Wade, & Day, 1987) that perceived distance interacts with compensation for head movements, but not with compensation-for eye movements with respect to a stationary head. In both experiments, when the vertically moving target was seen at a distance different from its physical distance, its perceived path was displaced relative to that seen when there was no error in pereived distance, or when it was pursued by eye movements alone. In a third experiment, simultaneous measurements of eye and head position during lateral head movements showed that errors in fixation were not sufficient to require modification of the retinal paths determined by the geometry of the observation conditions in Experiments 1 and 2.     

What are you looking at? Acuity for triadic eye gaze

The authors measured observers' ability to determine direction of gaze toward an object in space. In Experiment 1, they determined the difference threshold for determining whether a live "looker" was looking to the left or right of a target point. Acuity for eye direction was quite high (approximately 30 s arc). Viewing the movement of the looker's eyes did not improve acuity. When one of the looker's eyes was occluded, the observers' acuity was disrupted and their point of subjective equality was shifted away from the exposed eye. Experiment 2 was a replication of Experiment 1, but digitized gaze displays were used. The results of Experiment 3 showed that the acuity for direction of gaze depended on the position of the looker's target. Overall, the results indicated that humans are highly sensitive to gaze direction and that information from both eyes is used to determine direction of regard.     

Tactile orientation constancy: Do proprioception and attention affect the tactile vertical?1

Abstract: Tactile vertical, defined as the edge orientation that participants perceive to be vertical, was examined in four experiments. In Experiment 1, we touched the participants’ cheek, lips, or hand with an edge and asked them to judge its orientation with regard to gravitational vertical, both when the stimulated body part was upright (or, in the case of the lips, aligned), and when it was tilted (lips, distorted). We found that when the head or hand was tilted forward 30°, or when the lower lip was distorted approximately 38° to the left or right, the tactile vertical shifted in the same direction by only a fraction (8.7, 8.6, and 36.3% for the cheek, lips, and hand, respectively) of the change in orientation of the stimulated region. The results indicated considerable, but usually incomplete, orientation constancy. In Experiment 2, we measured tactile vertical on the hand for forward tilts from 0° to 45°. We found that as the hand was tilted, the tactile vertical increasingly shifted in the same direction as the hand (i.e., a tactile Aubert effect). In Experiment 3, the effect of attentional focus on tactile vertical was examined by comparing the tactile vertical of participants who attended to body‐centered coordinates, and others who attended to gravitation‐centered coordinates. We found that focusing on body‐centered coordinates caused a decrease in orientation constancy. We sought to examine the role of attention further in Experiment 4, measuring tactile vertical on the cheek of persons with temporomandibular disorders. Compared with normal participants, these participants displayed significantly lower constancy. The results were accounted for by a narrowing of attention to painful signals, so that proprioceptive information was attended to less. In conclusion, the degree of tactile orientation constancy that participants demonstrate varies as a function of body site and attentional focus.     

How trunk turns affect locomotion when you are not looking where you go

How well do we maintain heading direction during walking while we look at objects beside our path by rotating our eyes, head, or trunk? Common experience indicates that it may be fairly hazardous not to look where you are going. In the present study, 12 young adults walked on a treadmill while they followed a moving dot along a horizontal line with their gaze by rotating primarily either their eyes, head, or trunk for amplitudes of up to 25 degrees . During walking the movement of the center of pressure (COP) was monitored using force transducers under a treadmill. Under normal light conditions, the participants showed little lateral deviation of the COP from the heading direction when they performed the eye or head movement task during walking, even when optic flow information was limited. In contrast, trunk rotations led to a doubling of the COP deviation in the mediolateral direction. Some of this deviation was attributed to foot rotation. Participants tended to point their feet in the gaze direction when making trunk turns. The tendency of the feet to be aligned with the trunk is likely to be due to a preference to have feet and body in the same orientation. Such alignment is weaker for the feet with respect to head position and it is absent with respect to eye position. It is argued that feet and trunk orientation are normally tightly coupled during gait and that it requires special abilities to move both segments independently when walking.     

Apparent head position as a basis for a visual aftereffect of prolonged head tilt

A possible explanation of the visual spatial aftereffect following head tilt with eyes closed is that it is an outcome of a proprioceptive aftereffect of head position. If the upright head is apparently tilted then it might be expected that a vertical line in a dark room would also be apparently tilted. This explanation predicts that the direction and magnitude of the visual and proprioceptive aftereffects would correspond. The second of two experiments showed that the trends of the two aftereffects as a function of head tilt angle were different. It was concluded that the visual aftereffect cannot be explained in terms of a proprioceptive aftereffect.     

Visual perception of direction when voluntary saccades occur. I. Relation of visual direction of a fixation target extinguished before a saccade to a flash presented during the saccade

In experiments designed to clarify the mechanisms underlying the normal stability of visual direction for stationary objects when voluntary saccades occur, Ss reported on the horizontal visual direction of a brief test [lash presented when the eye was at a specific point in the saccade (the trigger point) relative to a fixation target viewed and extinguished prior to the saccade. From these reports, PSEs (points of subjective equality) were calculated for the fixation target as measured by the test [lashes. The distance of the trigger point from the previous fixation position was systematically varied in each experiment. Different experiments required saccades of different lengths and directions. With the exception of the presentation of the test [lash the saccades were carried out in complete darkness so that the possible utilization of an extraretinal signal regarding the eye movement (change in eye position, the intention to turn the eye, or a change of attention related to the eye movement) in the determination of visual direction could be observed uncomplicated by a continuing visual context. According to classical theories, an extraretinal signal proportional to the change in eye position acts to maintain direction constancy by compensating for the Shift of the retinal image resulting from the movement of the eye. In general, direction constancy was not preserved in the present experiments, and thus the data would not be predicted by classical theories. However, the PSE varied with distance of the trigger point from the fixation target. Since this displacement of PSE from the trigger point was in the correct direction for compensation, the presence of an extraretinal signal was confirmed. However, the growth of this signal appears to be time-locked to the saccade rather than locked to eye position; it is suggested that this growth takes place over a time period which is longer than the duration of the saccade itself.     

Auditory psychomotor coordination and visual search performance

In Experiments 1 and 2, the time to locate and identify a visual target (visual search performance in a two-alternative forced-choice paradigm) was measured as a function of the location of the target relative to the subject's initial line of gaze. In Experiment 1, tests were conducted within a 260 degree region on the horizontal plane at a fixed elevation (eye level). In Experiment 2, the position of the target was varied in both the horizontal (260 degrees) and the vertical (+/- 46 degrees from the initial line of gaze) planes. In both experiments, and for all locations tested, the time required to conduct a visual search was reduced substantially (175-1,200 msec) when a 10-Hz click train was presented from the same location as that occupied by the visual target. Significant differences in latencies were still evident when the visual target was located within 10 degrees of the initial line of gaze (central visual field). In Experiment 3, we examined head and eye movements that occur as subjects attempt to locate a sound source. Concurrent movements of the head and eyes are commonly encountered during auditorily directed search behavior. In over half of the trials, eyelid closures were apparent as the subjects attempted to orient themselves toward the sound source. The results from these experiments support the hypothesis that the auditory spatial channel has a significant role in regulating visual gaze.     

Constancy and illusion of apparent direction of rotary motion in depth: Tests of a theory

An explanation of apparent direction of rotary motion in depth derived from a general theory of perceptual constancy and illusion is proposed with experimental data in its support. Apparent direction of movement is conceived of as exhibiting-perceptual constancy or illusion as a function of apparent direction of orientation m depth for plane objects and apparent relative depth for three-dimensional objects. Apparent reversals of movement direction represent either regular fluctuations between constancy and illusion of direction as a function of valid and invalid stimuli for orientation, or irregular and random fluctuations in their absence. In three preliminary experiments, the apparent movement direction of plane ellipses was investigated as a function of surface pattern information for orientation, and in Experiment I apparent reversals during 20-revolution trials were studied. In Experiment II, apparent movement direction of 3D elliptical V shapes as a function of surface pattern information for relative depth was investigated. In addition to supporting the explanation proposed, the data offer a resolution of a conflict between different theories of apparent reversal of motion in depth.     

Motion parallax judgements of depth as a function of the direction and type of head movement

We compared the relative effectiveness of rotating or translating the head, either horizontally or vertically, on the perception of depth resulting from motion parallax. Using Rogers and Graham's (1979) paradigm, we yoked the movement of random dots on a screen to movements of the head, simulating a corrugated surface. In two experiments, subjects nulled the apparent depth or motion seen in the display. Horizontal head movements yielded the most precise depth judgements, irrespective of whether the head translated or rotated. Motion thresholds were higher than those for depth and were independent of direction of head movement. In a third experiment, suprathreshold stimuli that simulated differing amounts of depth were used, and the subjects' perception of depth was virtually the same for all types and directions of head movement. In our stimulus situation, rotating or translating the head either vertically or horizontally produced motion parallax cues for depth that were equally effective. Our results also showed that, within a range, retinal image motion from head movement is converted into a depth signal and that above that range location constancy breaks down and motion is seen.     

The response criterion,the stimulus configuration,and the relationship between brightness contrast and brightness constancy

Four experiments were designed to investigate the nature of the relationship between brightness contrast and brightness constancy while controlling the response criterion, the area of the surround, the stimulus configuration, and the mode of appearance of the modulus target. Ten Os in each of the four experiments estimated the apparent whiteness or brightness of targets with different contrast ratios. All targets were viewed at several illumination levels. Most constancy (whiteness and brightness) functions displayed shallow slopes that reflected a good approximation to constancy. The functions within Experiments I, III, and IV were vertically displaced and parallel; those in Experiment II were vertically displaced and increased in slope. This suggests that decreasing the contrast ratio had no effect on the tendency towards constancy when the area of the surround was greater than that of the target but resulted in a decrease in constancy when the area of the surround was equal to that of the target.