Biomedical subjects

Ian P Howard

Publications and source records attributed to Ian P Howard.

11 recordsLinked to original sources

PubMed2006

Illusory scene distortion occurs during perceived self-rotation in roll.

We report a novel illusory distortion of the visual scene, which became apparent during both: (i) observer rotation inside a furnished stationary room; and (ii) room rotation about the stationary observer. While this distortion had several manifestations, the most common experience was that scenery near fixation appeared to sometimes lead and other times lag more peripheral scenery. Across a series of experiments, we eliminated explanations based on eye-movements, distance misperception, peripheral aliasing, differential motion sensitivity and adaptation. We found that these illusory scene distortions occurred only when the observer perceived (real or illusory) changes in self-tilt and maintained a stable fixation.

Adult↗

PubMed2005

Effect of decorrelation on 3-D grating detection with static and dynamic random-dot stereograms.

Three experiments examined the effects of image decorrelation on the stereoscopic detection of sinusoidal depth gratings in static and dynamic random-dot stereograms (RDS). Detection was found to tolerate greater levels of image decorrelation as: (i) density increased from 23 to 676 dots/deg2; (ii) spatial frequency decreased from 0.88 to 0.22 cpd; (iii) amplitude increased above 0.5 arcmin; and (iv) dot lifetime decreased from 1.6s (static RDS) to 80 ms (dynamic RDS). In each case, the specific pattern of tolerance to decorrelation could be explained by its consequences for image sampling, filtering, and the influence of depth noise.

Adult↗

PubMed2005

Vertical-disparity gradients are processed independently in different depth planes.

We examined the effects of vertical-disparity gradients on apparent depth curvature of textured surfaces. In Experiment 1, vertical disparities induced expected curvatures when the surface had a horizontal disparity of < +/-40.34'. A central row of elements, lacking vertical disparities, ceased to have the same apparent curvature as the surface when the horizontal disparity between row and surface exceeded +/-5'. In Experiment 2, vertical disparities were not pooled between superimposed surfaces separated by horizontal disparities > +/-10'. Thus, vertical-disparity gradients are not pooled over depth for curvature perception. Our results suggest that vertical disparities are used to determine distances to surfaces directly, rather than to estimate vergence.

Adult↗

PubMed2005

Visual orientation in a mirror world tilted 90 degrees.

Previously, we showed that many supine observers in a furnished room tilted 90 degrees perceive themselves and the room as upright. We called this the "levitation illusion" because the arms feel weightless when held out from the body. We now report that a familiar scene viewed by supine observers through a mirror at 45 degrees appears vertical when, optically, it is horizontal and above the head. However, the body feels pitched upright only partially. This visual-righting effect, like the levitation illusion, is due to the polarity axis of the scene being accepted as vertical even in the presence of conflicting information from the gravity sense organs. In experiment 1 we tested the potency of objects containing either intrinsic polarity (due to familiar tops and bottoms) or extrinsic polarity (due to support relationships) to generate a visual-righting illusion. To almost all observers, a blank surface seen in the mirror appeared like a ceiling. A scene containing an object with intrinsic polarity, such as a chair or person, seen in the mirror appeared vertical to almost all observers. A scene containing a pair of objects with only extrinsic polarity, such as a ball on a shelf (but not a ball under a shelf), also appeared vertical to most observers. In experiment 2 we found that a polarised scene was more likely to produce a visual-righting illusion when it was arranged as a view through a window rather than as a picture inside a room.

Adolescent↗

PubMed2005

The effect of central and peripheral field stimulation on the rise time and gain of human optokinetic nystagmus.

We wished to examine the spatial (gain) and temporal (rise time) properties of human optokinetic nystagmus (OKN) as a function of stimulus velocity and field location. Stimuli were either M-scaled random dots or vertical stripes that moved at velocities between 20-80 deg s(-1). Three field conditions were examined: full field; a 20 deg central field; and a 12.5 deg central-field mask. OKN gain was found to be significantly affected by stimulus velocity and stimulus location, with the higher stimulus velocities and the 12.5 deg central-field mask giving lower gains. Steady-state gains for all three field conditions were not found to be affected by prior adaptation to stationary or moving stimuli. The 63% rise time was found to be significantly affected by the stimulus velocity, whereas this was not the case for the 90% rise time. Neither rise time was found to be significantly affected by the field location. These results indicate that, although the effectiveness (gain) of peripheral retina is lower than that of the central retina during optokinetic stimulation, the peripheral retina has access to common mechanisms responsible for the fast component of OKN.

Adaptation, Ocular↗

PubMed2004

Detection of the depth order of defocused images.

The sign of an accommodative response is provided by differences in chromatic aberration between under- and over-accommodated images. We asked whether these differences enable people to judge the depth order of two stimuli in the absence of other depth cues. Two vertical edges separated by an illuminated gap were presented at random relative distances. Exposure was brief, or prolonged with fixed or changing accommodation. The gap was illuminated with tungsten light or monochromatic light. Subjects could detect image blur with brief exposure for both types of light. But they could detect depth order only in tungsten light with long exposure, with or without changes in accommodation.

Accommodation, Ocular↗

PubMed2004

The stimulus integration area for horizontal vergence.

Over what region of space are horizontal disparities integrated to form the stimulus for vergence? The vergence system might be expected to respond to disparities within a small area of interest to bring them into the range of precise stereoscopic processing. However, the literature suggests that disparities are integrated over a fairly large parafoveal area. We report the results of six experiments designed to explore the spatial characteristics of the stimulus for vergence. Binocular eye movements were recorded using magnetic search coils. Each dichoptic display consisted of a central target stimulus that the subject attempted to fuse, and a competing stimulus with conflicting disparity. In some conditions the target was stationary, providing a fixation stimulus. In other conditions, the disparity of the target changed to provide a vergence-tracking stimulus. The target and competing stimulus were combined in a variety of conditions including those in which (1) a transparent textured-disc target was superimposed on a competing textured background, (2) a textured-disc target filled the centre of a competing annular background, and (3) a small target was presented within the centre of a competing annular background of various inner diameters. In some conditions the target and competing stimulus were separated in stereoscopic depth. The results are consistent with a disparity integration area with a diameter of about 5 degrees. Stimuli beyond this integration area can drive vergence in their own right, but they do not appear to be summed or averaged with a central stimulus to form a combined disparity signal. A competing stimulus had less effect on vergence when separated from the target by a disparity pedestal. As a result, we propose that it may be more useful to think in terms of an integration volume for vergence rather than a two-dimensional retinal integration area.

Adult↗

PubMed2003

Monocular transparency generates quantitative depth.

Monocular zones adjacent to depth steps can create an impression of depth in the absence of binocular disparity. However, the magnitude of depth is not specified. We designed a stereogram that provides information about depth magnitude but which has no disparity. The effect depends on transparency rather than occlusion. For most subjects, depth magnitude produced by monocular transparency was similar to that created by a disparity-defined depth probe. Addition of disparity to monocular transparency did not improve the accuracy of depth settings. The magnitude of depth created by monocular occlusion fell short of that created by monocular transparency.

Adult↗

PubMed2003

Neurons that respond to more than one depth cue.

The 3D orientation of a surface can be specified by perspective, motion parallax or binocular disparity. Tsutsui et al. have found cells in the monkey intraparietal sulcus that responded to surface orientation defined only by a texture gradient. Most of these cells also responded to orientation defined only by binocular disparity.

Animals↗

PubMed2002

The cyclopean eye in vision: the new and old data continue to hit you right between the eyes.

We argue against recent claims by Erkelens and van Ee (Vision Res., in press) and by Erkelens (Vision Res. 40 (2000) 2411) that "the concept of the cyclopean eye is em leader always irrelevant as far as vision is concerned" (p. 1157) [corrected] and that "perceived direction during monocular viewing is based on the signals of the viewing eye only" (p. 2411), respectively. In Experiment 1, we presented a pair of small lights on a visual axis and measured the absolute visual direction of the near light with reference to different parts of the face. The near light appeared in front of the bridge of the nose or very near it, contrary to what was expected from Erkelens and van Ee's claim that monocular stimuli are seen in their correct locations. In Experiment 2, we replicated Erkelens' experiments with measurements of phoria and analyses of eye movements. The results confirmed his finding that the cyclopean illusion occurred rarely in the monocular condition, but our phoria and eye movement data provided the basis for a very different interpretation. Our data show that the oculomotor signal in his particular monocular condition was considerably weaker than in his binocular condition; therefore, the rarity of the monocular cyclopean illusion is not surprising. Moreover, since both claims above are based on an over-generalization of the results of Erkelens' study, neither claim is persuasive.

Adult↗

PubMed2002

Perception of self-tilt in a true and illusory vertical plane.

A tilted furnished room can induce strong visual reorientation illusions in stationary subjects. Supine subjects may perceive themselves upright when the room is tilted 90 degrees so that the visual polarity axis is kept aligned with the subject. This 'upright illusion' was used to induce roll tilt in a truly horizontal, but perceptually vertical, plane. A semistatic tilt profile was applied, in which the tilt angle gradually changed from 0 degrees to 90 degrees, and vice versa. This method produced larger illusory self-tilt than usually found with static tilt of a visual scene. Ten subjects indicated self-tilt by setting a tactile rod to perceived vertical. Six of them experienced the upright illusion and indicated illusory self-tilt with an average gain of about 0.5. This value is smaller than with true self-tilt (0.8), but comparable to the gain of visually induced self-tilt in erect subjects. Apparently, the contribution of nonvisual cues to gravity was independent of the subject's orientation to gravity itself. It therefore seems that the gain of visually induced self-tilt is smaller because of lacking, rather than conflicting, nonvisual cues. A vector analysis is used to discuss the results in terms of relative sensory weightings.

Adult↗