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Visual spatial illusions: a general explanation.

Representation at the visual receptors of such properties of the object as its size, shape, orientation, and movement undergo considerable variation as the distance, bearing, posture, and motion of the observer, relative to the object, changes. However, despite these gross and frequent deformations of the image, perceived properties remain extraordinarily stable. Such constancy has obvious biological utility; the observer perceives his world according to its fixed physicalfeatures rather than in terms of its variable sensory representation. Constancy of apparent size, shape, orientation, and movement is dependent on information for the distance, bearing, lateral tilt, and movement of the observer, respectively. Thus, as the retinal image shrinks with distance, constancy of apparent size is maintained by five classes of distance, stimuli that operate singly or in various combinations. Likewise, visual orientation and visual stimuli for the orientation of the observer, and movement constancy on visual and nonvisual stimuli for the movement of the observer. Illusion occur when stimuli that normally preserve constancy are operative but with the image of the object not varied. Thus if retinal disparity, convergence-accommodation, projected stimuli, or other distance stimuli are varied with the image not varied, illusions of size occur. Those rsluting from variation of projected stimuli are the. well-known geometrical size illusions and include the Mü llerLyer group. In essentially the same manner, independent manipulation of stimuli for the orientation and the motion of the observer, with the orientation and the motion of the image at the retina not varied, gives rise to illusory orientations and movements of the object. Limited attempts to explain size illusions in terms of the projected stimuli that preserve perceptual constancy are by no means new; Thiéry (51) proposed such a view in the later part of the last century, and in recent times there has been a spate of such proposals including the " misapplied constancy hypothesis" advanced by Gregory (2). However, Gregory's theory is confined largely to geometrical size illusions and invoks only distance scaling given by a limited number of projected stimuli. Furthermore, the Müller-Lyer illusion is seen by him to be a consequence of distance scaling resulting from the converging arrows. There is no recognition of the range of such effects with various attached elements, as shown in Fig3, and no attention is accorded the recently established difference between the illusions with inward and outward-directed elements. The theory of spatial illusions outlined here distinguishes between classes of illusory effect and, in linking each to its particular class of spatial constancy, offers a general and testable explanation. Failure to recognize classes of illusion(and perceptual constancy), such as those of size, orientation, and movement, can be regarded as among the major deficiencies of recent attempts (2, 44) to explain illusory effects. I do not claim that this explanation, which I call the general constancy theory, satisfactorily encómpasses all known illusions, but merely that it is more comprehensive than alternative explantions I conclude that any stimulus which serves to maintain perceptual constancy of a property of an object as the visual representation of that property varies will, when independently manipulated with the retinal image not varied, produce an illusion. This general principle predictS the conditions under which illusory effects will occur and has wide explanatory application.

Age Factors↗

Honeybee navigation: nature and calibration of the "odometer".

There are two theories about how honeybees estimate the distance to food sources. One theory proposes that distance flown is estimated in terms of energy consumption. The other suggests that the cue is visual, and is derived from the extent to which the image of the world has moved on the eye during the trip. Here the two theories are tested by observing dances of bees that have flown through a short, narrow tunnel to collect a food reward. The results show that the honeybee's "odometer" is visually driven. They also provide a calibration of the dance and the odometer in visual terms.

Animals↗

Spatial memory of body linear displacement: what is being stored?

The ability to evaluate traveled distance is common to most animal species. Head trajectory in space is measured on the basis of the converging signals of the visual, vestibular, and somatosensory systems, together with efferent copies of motor commands. Recent evidence from human studies has shown that head trajectory in space can be stored in spatial memory. A fundamental question, however, remains unanswered: How is movement stored? In this study, humans who were asked to reproduce passive linear whole-body displacement distances while blindfolded were also able to reproduce velocity profiles. This finding suggests that a spatiotemporal dynamic pattern of motion is stored and can be retrieved with the use of vestibular and somesthetic cues.

Acceleration↗

Distance stereoacuity in intermittent exotropia.

BACKGROUND: Studies of distance stereoacuity in intermittent exotropia suggest that normal stereoacuity corresponds to good control of the deviation and that reduced or negative stereoacuity signifies poorer control. AIM: : To evaluate distance stereoacuity in intermittent exotropia using the Frisby Davis Distance stereo test (FD2). METHODS: Children with intermittent exotropia where the near angle was less than or equal to distance were eligible for recruitment. Standardised prospective data collection included FD2 distance stereoacuity. This was a longitudinal study in which outcomes are reported for baseline, last follow-up (> or =6 months before any surgery) or preoperative and last postoperative visits for those undergoing surgery. RESULTS: 110 children with intermittent exotropia had FD2 stereoacuity tested at baseline: 70 comprehended the test. Mean (standard deviation (SD)) age was 4.6 (1.7) years (range 2-10 years). 41/70 (59%) showed positive responses: mean (SD) stereoacuity 30 (12) s of arc. The mean follow-up period before any surgery was 13 months (range 6-27 months). At follow-up, mean (SD) stereoacuity was 24 (11) s of arc. Preoperative and postoperative stereoacuity were not significantly different from those not undergoing surgery. CONCLUSION: This study was the first to report distance stereoacuity in intermittent exotropia using the FD2 stereo test: patients with intermittent exotropia can achieve normal levels of distance stereoacuity, but a considerable proportion, despite comprehending, showed a negative response. This suggests that using the FD2, distance stereoacuity in intermittent exotropia is either absent or normal rather than reduced. Possible reasons for this and its implications are discussed.

Child↗

Genetic analysis of cover test measures and AC/A ratio in human populations with varying incidences of strabismus.

The genetic analyses of indices relating to distance alignment and accommodative convergence are presented. This approach is important in understanding the contribution of genetic factors to observed individual differences for these measures. Abnormalities of either of these two components results in a tendency towards either a convergent or divergent position of the eyes (relative to the position of fusional demand) and thus places an additional load or strain on the other components of the binocular mechanism which must compensate for this potential disruption. If compensation is inadequate to maintain alignment of the eyes, a manifest deviation will result. Consequently, an understanding of the aetiology of such factors underlies an understanding of the aetiology of nonparalytic strabismus. The three populations displayed different tendencies in the cover test measure. The average tendency for each of the populations was consistent with the type of deviation common to all propositi of families within each of the respective populations. The heritability of this character was similar in the three populations and was dependent on the contribution of the female parent only, but to a substantial degree (h2 = 0-42 +/- 0-12). The nature of the sex difference is at present open to speculation. The population means within generations were similar for the gradient measure of AC/A ratio. The heritability of this character (0-38 +/- 0-09) suggests that the genetic component is of substantial importance underlying individual differences for AC/A ratio.

Accommodation, Ocular↗

Preliminary results of a physiologically based treatment of amblyopia.

An apparatus has been developed in which high-contrast square-wave gratings are rotated in front of the amblyopic eye while the child is performing some task requiring visual concentration. In the course of three 7-minute treatments 73% of patients treated achieved 6/12 or better; 75% of these patients had previously undertaken conventional or minimal occlusion.

Amblyopia↗

Amblyopia: is visual loss permanent?

AIM: To ascertain whether recovery of visual function in amblyopic eyes is likely to occur when the fellow eye is lost as a result of age related macular degeneration. METHODS: The records of 465 patients with an established diagnosis of age related macular degeneration who had attended a specialist macular clinic between 1990 and 1998 were scrutinised. A full clinical examination and standardised refraction had been carried out in 189 of these cases on a minimum of two occasions. Cases were looked for where an improvement of one or more lines of either distance or near acuity was recorded in the eye unaffected by macular disease. In each one of these cases the improvement in visual acuity could not be attributed to treatment of other existing pathology. RESULTS: 12 such cases were detected. In nine of these the eye showing improvement of acuity had a history of amblyopia. The mean improvement in distance and near acuity in amblyopic eyes by 12 months was 3.3 and 1.9 lines logMAR respectively. The improvement in acuity generally occurred between 1 and 12 months from baseline and remained stable over the period of follow up. CONCLUSIONS: Older people with a history of amblyopia who develop visual loss in the previously normal eye can experience recovery of visual function in the amblyopic eye over a period of time. This recovery in visual function occurs in the wake of visual loss in the fellow eye and the improvement appears to be sustained.

Amblyopia↗

Reliability of distance estimation by doctors and patients: cross sectional study.

OBJECTIVE: To assess the reliability and accuracy of distance estimated by doctors and patients. DESIGN: Comparison between estimated and measured distances of six familiar sites around Guy's Hospital, London. SUBJECTS: 100 hospital consultants and 100 patients. MAIN OUTCOME MEASURES: Median (range) of estimated distances, and mean (SD) of the difference between estimated and measured distances. RESULTS: Both doctors and patients gave a wide range of estimates of distance. The estimates differed by up to 14.6-fold from the measured distances, and the difference between minimum and maximum estimates was up to 62.5-fold. CONCLUSION: Doctors and patients were inaccurate at estimating distances, which implies that estimates of distances walked are not reliable indicators of a person's health.

Cross-Sectional Studies↗

Neuronal correlates of face identification in the monkey anterior temporal cortical areas.

To investigate the neuronal basis underlying face identification, the activity of face neurons in the anterior superior temporal sulcus (STS) and the anterior inferior temporal gyrus (ITG) of macaque monkeys was analyzed during their performance of a face-identification task. The face space was composed by the activities of face neurons during the face-identification task, based on a multidimensional scaling (MDS) method; the face space composed by the anterior STS neurons represented facial views, whereas that composed by the anterior ITG neurons represented facial identity. The temporal correlation between the behavioral reaction time of the animal and the latency of face-related neuronal responses was also analyzed. The response latency of some of the face neurons in the anterior ITG exhibited a significant correlation with the behavioral reaction time, whereas this correlation was not significant in the anterior STS. The correlation of the latency of face-related neuronal responses in the anterior ITG with the behavioral reaction time was not found to be attributed to the correlation between the response latency and the magnitude of the neuronal responses. The present results suggest that the anterior ITG is closely related to judgments of facial identity, and that the anterior STS is closely related to analyses of incoming perceptual information; face identification in monkeys might involve interactions between the two areas.

Action Potentials↗

A neural network model of flexible spatial updating.

Neurons in many cortical areas involved in visuospatial processing represent remembered spatial information in retinotopic coordinates. During a gaze shift, the retinotopic representation of a target location that is fixed in the world (world-fixed reference frame) must be updated, whereas the representation of a target fixed relative to the center of gaze (gaze-fixed) must remain constant. To investigate how such computations might be performed, we trained a 3-layer recurrent neural network to store and update a spatial location based on a gaze perturbation signal, and to do so flexibly based on a contextual cue. The network produced an accurate readout of target position when cued to either reference frame, but was less precise when updating was performed. This output mimics the pattern of behavior seen in animals performing a similar task. We tested whether updating would preferentially use gaze position or gaze velocity signals, and found that the network strongly preferred velocity for updating world-fixed targets. Furthermore, we found that gaze position gain fields were not present when velocity signals were available for updating. These results have implications for how updating is performed in the brain.

Animals↗

Motor scaling by viewing distance of early visual motion signals during smooth pursuit.

The geometry of gaze stabilization during head translation requires eye movements to scale proportionally to the inverse of target distance. Such a scaling has indeed been demonstrated to exist for the translational vestibuloocular reflex (TVOR), as well as optic flow-selective translational visuomotor reflexes (e.g., ocular following, OFR). The similarities in this scaling by a neural estimate of target distance for both the TVOR and the OFR have been interpreted to suggest that the two reflexes share common premotor processing. Because the neural substrates of OFR are partly shared by those for the generation of pursuit eye movements, we wanted to know if the site of gain modulation for TVOR and OFR is also part of a major pathway for pursuit. Thus, in the present studies, we investigated in rhesus monkeys whether initial eye velocity and acceleration during the open-loop portion of step ramp pursuit scales with target distance. Specifically, with visual motion identical on the retina during tracking at different distances (12, 24, and 60 cm), we compared the first 80 ms of horizontal pursuit. We report that initial eye velocity and acceleration exhibits either no or a very small dependence on vergence angle that is at least an order of magnitude less than the corresponding dependence of the TVOR and OFR. The results suggest that the neural substrates for motor scaling by target distance remain largely distinct from the main pathway for pursuit.

Acceleration↗