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PubMed1998

A computational model of depth perception based on headcentric disparity.

It is now well established that depth is coded by local horizontal disparity and global vertical disparity. We present a computational model which explains how depth is extracted from these two types of disparities. The model uses the two (one for each eye) headcentric directions of binocular targets, derived from retinal signals and oculomotor signals. Headcentric disparity is defined as the difference between headcentric directions of corresponding features in the left and right eye's images. Using Helmholtz's coordinate systems we decompose headcentric disparity into azimuthal and elevational disparity. Elevational disparities of real objects are zero if the signals which contribute to headcentric disparity do not contain any errors. Azimuthal headcentric disparity is a 1D quantity from which an exact equation relating distance and disparity can be derived. The equation is valid for all headcentric directions and for all binocular fixation positions. Such an equation does not exist if disparity is expressed in retinal coordinates. Possible types of errors in oculomotor signals (six) produce global elevational disparity fields which are characterised by different gradients in the azimuthal and elevational directions. Computations show that the elevational disparity fields uniquely characterise both the type and size of the errors in oculomotor signals. Our model uses a measure of the global elevational disparity field together with local azimuthal disparity to accurately derive headcentric distance throughout the visual field. The model explains existing data on whole-field disparity transformations as well as hitherto unexplained aspects of stereoscopic depth perception.

Computational Biology↗
PubMed1991

Temporal limits of the susceptibility of depth perception to proprioceptive deafferentations of extraocular muscles.

In a previous study, extraocular muscle proprioception (E.O.M.P.) was shown to play an important role in the postnatal development of depth perception: following unilateral or bilateral sections of the ophthalmic branch of the trigeminal nerve (V1th nerve) performed at 6-8 weeks of age, the binocular thresholds were 2 to 3 times higher than in control animals. Since the V1-sections produced no deficits when performed in adults, the temporal limits of a period of susceptibility remained to be determined. In order to assess the lower and upper limits of the period during which these perceptual deficits could be induced, unilateral or bilateral V1-sections were performed in kittens at different ages. Depth perception thresholds were measured by using the jumping stand technique. Sections of the V1 nerve only produced significant impairments of the binocular depth thresholds when performed after 3 weeks of age. They could be observed when unilateral sections were performed at up to 13 weeks of age and with bilateral sections at up to 10 weeks of age. These functional impairments appeared to remain permanently through adult life.

Animals↗
PubMed1998

Defaults in stereoscopic and kinetic depth perception.

This study presents three findings concerning the mechanisms of depth perception. First, the shape of the three-dimensional percept evoked by two-frame motion is defined solely by the rotation component around an axis in the frontoparallel plane; the visual system assigns a default value to this rotation component to arrive at a unique solution. Second, when the visual axes of two eyes are almost parallel, the visual system uses a default vergence value to reconstruct stereoscopic depth. Third, the default vergence and default rotation angles are highly correlated across subjects. This correlation implies that the two modalities share a common scaling default at an internal level.

Cues↗
PubMed1979

Assessment of depth perception in cats.

A behavioural method is described for the assessment of depth perception of kittens. Measurement is made of the smallest separation in depth that can be discriminated between two adjacent stimuli under both monocular and binocular viewing conditions. Normal animals can discriminate much smaller separations in depth when using two eyes than with monocular viewing, implying the presence of a cue to depth that is uniquely available with binocular viewing. The test provides a quick and reliable way of screening animals for stereopsis.

Animals↗
PubMed1992

Factors that affect depth perception in stereoscopic displays.

This study investigated several factors that affect depth perception in stereoscopic displays: half-image separation magnitude, separation direction (crossed vs. uncrossed), viewing distance, stimulus size, and exposure duration. The depth perceived under various combinations of levels of these factors was compared with depth predicted by the geometry of stereopsis. Perceived depth in the crossed-separation direction was frequently close to predictions, such that increases in separation and viewing distance produced appropriate increases in perceived depth. Depth in the uncrossed direction was frequently less than that predicted, especially for small stimuli presented at a long viewing distance, with a large half-image separation, and/or with a brief duration. Thus depth in both crossed and uncrossed directions equaled predictions only for large stimuli exposed for a long duration.

Adult↗
PubMed1996

Remote operation: a selective review of research into visual depth perception.

Some perceptual motor operations are performed remotely; examples include the handling of life-threatening materials and surgical procedures. A camera conveys the site of operation to a TV monitor, so depth perception relies mainly on pictorial information, perhaps with enhancement of the occlusion cue by motion. However, motion information such as motion parallax is not likely to be important. The effectiveness of pictorial information is diminished by monocular and binocular information conveying flatness of the screen and by difficulties in scaling: Only a degree of relative depth can be conveyed. Furthermore, pictorial information can mislead. Depth perception is probably adequate in remote operation, if target objects are well separated, with well-defined edges and familiar shapes. Stereoscopic viewing systems are being developed to introduce binocular information to remote operation. However, stereoscopic viewing is problematic because binocular disparity conflicts with convergence and monocular information. An alternative strategy to improve precision in remote operation may be to rely on individuals who lack binocular function: There is redundancy in depth information, and such individuals seem to compensate for the lack of binocular function.

Depth Perception↗
PubMed1981

Depth perception in linear and inverse perspective pictures.

The range of pictorial depth perception was tested with four pictures from the repertoire of European art, rather than the customary line drawings or photographs. These pictures included those rendered in linear perspective and inverse perspective, as well as those with different degrees of depth. Using Pandora' Box, the subjects were asked to place a lamp at the same apparent depth as objects in the pictures. The subjects did so without regard to the depiction technique. The results suggest that depth is seen in pictures both where the rules of linear perspective hold and where they have been violated.

Art↗
PubMed2001

Stereoacuity and depth perception decrease with increased instrument magnification: comparing a non-magnified system with lens loupes and a surgical microscope.

PURPOSE: To evaluate the effect of instrument magnification used in eye surgery on stereoacuity and depth perception. METHODS: Twenty-one subjects (10 clinical ophthalmologists familiar with loupes and operating microscopes and 11 non-ophthalmologists) with normal near vision and stereoacuity were tested with the Randot Stereotest viewed unmagnified, with a 4x loupes (450 mm focal length), and with a 16x operating microscope. RESULTS: Total scores: 8 errors in 210 test steps with the unmagnified observations, 25/210 with loupes, and 30/210 with the microscope. The statistical differences in these scores were "statistically highly significant" for all three tests (p = 0.002); and "significant" for the unmagnified versus loupe (p = 0.007) and unmagnified versus microscope (p = 0.002). Test viewing through the microscope, the greatest errors occurred (total errors = 1840 seconds of arc), less with the loupes (total 1150") and least without magnification (total 220"). Errors and scores for 10 experienced ophthalmologists were no different (p > or = 0.55, p = 1.00) from the 11 non-ophthalmologist subjects. CONCLUSIONS: Stereoacuity and depth perception decrease when viewing a test target with loupes or with a microscope, with the effect worsening as magnification increases. Familiarity with the magnifying equipment did not improve stereoacuity.

Adult↗
PubMed1993

Optic flow and depth perception.

The field of depth recovery from optic flow has recently experienced much growth, both on the theoretical and on the empirical fronts. Unfortunately, the theoretical results are not as widely known to perception workers as they might be. This article gives a simple analysis of the information for depth present in optic flow. It also reviews the psychophysical results for depth recovery from motion. These results are discussed with reference to the theoretical analysis and to relevant computer algorithms for depth recovery.

Algorithms↗
PubMed1993

The familiar-size cue to distance and stereoscopic depth perception.

The role of the familiar-size cue to distance in stereoscopic depth perception was examined in two experiments. In experiment 1 subjects judged the depth of a binocularly viewed interval, the far point of which was defined by either a familiar or an unfamiliar object, and in experiment 2 subjects adjusted the depth of the interval so that its extent appeared equal to the length of a vertical reference extent positioned on the surface of the object. Although familiar size influenced depth estimates (experiment 1) it did not influence matching judgments (experiment 2). The findings are discussed with reference to the issue of the nature of the familiar-size effects on judgments of stereoscopic depth.

Depth Perception↗
PubMed2005

Binocular depth perception from unpaired image points need not depend on scene organization.

Dichoptic stimuli containing unmatched features can produce depth perception despite the absence of binocular disparity, a phenomenon known as da Vinci stereopsis. Unmatched points can arise from depth discontinuities and partial occlusion in the real world. It has been hypothesized that spatial organization of unmatched image features as dictated by the ecological optics of occlusion might determine perceived depth in da Vinci stereopsis. We tested this hypothesis by creating dichoptic stimuli containing unmatched points in which local cues and overall organization could be dissociated. For these stimuli, observers' perception of depth did not depend on the organization of the scene, but only on the local cues. This finding shows the perceived depth of unpaired points need not depend on reconstructing the spatial organization of depth discontinuities in real-world scenes.

Depth Perception↗
PubMed2005

Cross-modal activation of visual cortex during depth perception using auditory substitution of vision.

Previous neuroimaging studies identified multimodal brain areas in the visual cortex that are specialized for processing specific information, such as visual-haptic object recognition. Here, we test whether visual brain areas are involved in depth perception when auditory substitution of vision is used. Nine sighted volunteers were trained blindfolded to use a prosthesis substituting vision with audition both to recognize two-dimensional figures and to estimate distance of an object in a real three-dimensional environment. Using positron emission tomography, regional cerebral blood flow was assessed while the prosthesis was used to explore virtual 3D images; subjects focused either on 2D features (target search) or on depth (target distance comparison). Activation foci were found in visual association areas during both the target search task, which recruited the occipito-parietal cortex, and the depth perception task, which recruited occipito-parietal and occipito-temporal areas. This indicates that some brain areas of the visual cortex are relatively multimodal and may be recruited for depth processing via a sense other than vision.

Acoustic Stimulation↗
PubMed2003

Behavioural-analytical studies of the role of head movements in depth perception in insects, birds and mammals.

In this review, studies of the role of head movements in generating motion parallax which is used in depth perception are examined. The methods used and definitiveness of the results vary with the animal groups studied. In the case of insects, studies which quantify motor outputs have provided clear evidence that motion parallax evoked by head movements is used for distance estimation and depth perception. In the case of birds and rodents, training studies and analyses of the head movements themselves have provided similar indications. In the case of larger mammals, due to a lack of systematic experiments, the evidence is less conclusive.

Journal Article↗
PubMed1996

Stability of binocular depth perception with moving head and eyes.

We systematically analyse the binocular disparity field under various eye, head and stimulus positions and orientations. From the literature we know that certain classes of disparity which involve the entire disparity field (such as those caused by horizontal lateral shift, differential rotation, horizontal scale and horizontal shear between the entire half-images of a stereogram) lead to relatively poor depth perception in the case of limited observation periods. These classes of disparity are found to be similar to the classes of disparities which are brought about by eye and head movements. Our analysis supports the suggestion that binocular depth perception is based primarily (for the first few hundred milliseconds) on classes of disparity that do not change as a result of ego-movement.

Depth Perception↗
PubMed1986

Attention and depth perception.

The Necker cube is a line drawing with two possible solutions in depth perception. The process of interpreting a two-dimensional line drawing as a three-dimensional object was investigated using the Necker cube. Attention was directed to a local feature of a briefly presented cube, ie an angle at a vertex. The attended angle was perceived as a front part of the cube and other parts were interpreted so as to match this interpretation. Results show that the local feature to which attention was directed was interpreted first and then global features and other local features were interpreted so as to agree with the local feature interpreted initially. This suggests that the three-dimensional interpretation of the line drawing was made sequentially from the local feature to global structures.

Attention↗
PubMed2000

Neural substrates for depth perception of the Necker cube; a functional magnetic resonance imaging study in human subjects.

We have studied the cerebral activity for the depth perception of the Necker cube by functional magnetic resonance imaging. Three types of line drawing figures were used as stimuli, the Necker cube, hidden line elimination cube and overlapping squares. Subjects were instructed to perceive both orientations of the depth of the Necker cube. They were instructed to shift their attention voluntarily during viewing overlapping squares to obtain a control for the attentional shift in perceiving the Necker cube. A hidden line elimination cube was used as a control for monocular stereopsis. The results showed a clear symmetrical activation in premotor and parietal areas during the Necker cube perception compared with other conditions. The present result suggests that a neural process similar to mental image manipulation occurs during depth perception of the Necker cube.

Brain Mapping↗