Biomedical subjects

Ian P Howard

Publications and source records attributed to Ian P Howard.

5 recordsLinked to original sources

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↗