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D Regan

Publications and source records attributed to D Regan.

At least 19 recordsLinked to original sources
PubMed1992

Motion-defined letter detection and recognition in patients with multiple sclerosis.

Two important distinctions in visual perception are (1) between the detection and recognition of shape (e.g., letters), and (2) between the recognition of shapes defined by a difference in brightness and the recognition of shapes defined by a difference in motion. We report that 6 of 10 patients with multiple sclerosis showed impaired recognition for motion-defined (MD) letters, although the detection of MD letters was normal as were both detection and recognition of luminance-defined letters. We have shown that this was not a function of acuity loss or the loss of ability to detect motion or a general failure of recognition per se, but was confined to a loss of ability to recognize MD letters. The neurological implications of these findings are discussed, and it is suggested that the MD letter test be used by others interested in the central pathology of visual disorders.

Adult↗
PubMed1992

Shape discrimination and the judgement of perfect symmetry: dissociation of shape from size.

We measured the accuracy with which subjects judged that a square or circle was perfectly symmetrical i.e. that aspect ratio (a/b) was exactly unity (where a and b were, respectively, the vertical and horizontal dimensions). Errors were remarkably small, ranging from 0.7 to 0.4% for the judgement of squareness and from 1.4 to < 0.1% for the judgement of circularity. Precision in judging aspect ratio was measured by requiring subjects to judge whether the aspect ratio (a/b)TEST of a test rectangle was greater or less than the aspect ratio (a/b)REF of a reference rectangle. Similar measurements were made for elliptical targets. To ensure that subjects based judgements on aspect ratio rather than a, b or (a-b), the area of each successive presentation was varied randomly. The just-discriminable percentage change of aspect ratio was as low as 1.6% at (a/b)REF = 1.0 (i.e. for a square or circular reference), and rose progressively as (a/b)REF was made progressively larger or smaller than 1.0. Aspect ratio discrimination threshold was independent of mean area over a sixteen-fold range of 0.25-4.0 deg2. For both rectangles and ellipses, the best value of aspect ratio discrimination threshold corresponded to a precision of encoding a and b of 14 sec arc or better. In further experiments, the method of constant stimuli was used to measure an aspect ratio aftereffect produced by adapting separately to rectangles of (a/b)ADAPT equal to 1.5, 1.0 and (1/1.5). Similar aftereffects were obtained whether the area of the test stimulus was fixed or varied randomly from trial to trial, and whether the test stimulus was rectangular or elliptical. The aftereffect could not be explained in terms of fatigue of neurons sensitive to linear dimension a or b. Nor could the aftereffect be explained in terms of the "contour repulsion" hypothesis, or in terms of orientation discrimination. We conclude (1) that the same neural mechanism determines aspect ratio discrimination threshold for rectangles and ellipses and (2) that this mechanism is sensitive to aspect ratio independently of linear dimensions. We propose that aspect ratio perception is determined by the balance of excitation of two pools of neurons that are selectively sensitive to different, but overlapping ranges of (a/b). One pool prefers aspect ratios > 1.0 and the others prefer aspect ratios < 1.0. We suppose that the two pools respond identically to changes in area (a * b).(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Ocular↗
PubMed1992

Dissociation of orientation discrimination from form detection for motion-defined bars and luminance-defined bars: effects of dot lifetime and presentation duration.

A stationary bar-shaped area that was perfectly camouflaged within a dot pattern was rendered visible by moving the dots inside and outside the bar at equal and opposite speeds. Orientation discrimination for this motion-defined (MD) bar was compared with orientation discrimination for a luminance-defined (LD) bar created by switching off all dots outside the bar. The best values of orientation discrimination threshold were similar for MD and LD bars at long presentation durations and long dot lifetimes. But, as presentation duration or dot lifetime was reduced below 1.0 sec, orientation discrimination threshold for MD bars increased at an accelerating rate, while discrimination for LD bars was comparatively unaffected. However, these effects of presentation duration and dot lifetime were largely due to changes in bar visibility. When bar visibility was normalised relative to the relevant bar detection threshold, the effect of presentation duration upon orientation discrimination was abolished for both MD and LD bars, and the effect of dot lifetime was abolished or even reversed. These observations dissociate detection and discrimination for MD and LD form. We suggest that orientation discrimination for MD and LD bars is determined by opponent-orientation mechanisms whose performance is not directly affected by presentation duration, nor degraded by reducing dot lifetime.

Adolescent↗
PubMed1992

Visual judgements and misjudgements in cricket, and the art of flight.

To hit the ball with the centre of percussion of a bat so that the ball goes where he intends it to go, a batsman must estimate visually where the ball will be at a specific future time (when), and coordinate his swing accordingly. A number of visual cues are available to the batsman. Retinal image information provides an accurate indication of time to contact (ie when), even when the trajectory of the ball is inclined to the line of sight, and there is evidence that the human visual system is specifically sensitive to time-to-contact information. But only part of the necessary information about position (ie where) is available to the batsman. If the batsman's head is directly in the line of flight, the velocity ratio of the retinal images in the left and right eyes provides a precise cue to the trajectory of the ball in the horizontal plane. However, humans have only poor visual sensitivities to the absolute distance and to the line-of-sight velocity of a ball. Therefore, a batsman has inadequate retinal image information about the absolute vertical velocity of a ball. It is suggested in this paper that batsmen supplement inadequate retinal image information about where the ball will hit the ground with prior knowledge built up over the preceding few deliveries. Some slow bowlers can induce the batsman to misjudge where the ball will hit the ground. I suggest that these bowlers manipulate the flight of the ball so as to induce the batsman to supplement his inadequate retinal image information with inappropriate prior knowledge, and thus to misinterpret the vertical angular speed of the retinal image of the ball.

Animals↗
PubMed1992

Method for identifying amblyopes whose reduced line acuity is caused by defective selection and/or control of gaze.

Three visual tests were administered to a group of 15 amblyopic children, 15 adult amblyopes and two age-matched control groups, each of 20 subjects. Test results comprised visual acuity for recognizing high contrast letters presented in line (i.e. Snellen) format, isolated-letter format and repeat-letter format. The classical Snellen format confounds the effects of gaze control defects with the effects of adjacent contours on a patient's ability to recognize a foveated letter. We designed a repeat-letter format intended to unconfound these effects. The repeat letter format is much less sensitive to gaze control defects, and somewhat more sensitive to adjacent contour interactions than is the Snellen format. We report that amblyopic eyes can be subdivided empirically into three repeat-letter categories: repeat-letter acuity significantly better than Snellen acuity; repeat letter acuity not significantly different from Snellen acuity; and repeat letter acuity significantly worse than Snellen acuity. We report that this subdivision cuts across the clinical subclassification of amblyopia and also across the crowding/no crowding subclassification. We suggest that, rather than abnormal lateral interactions, defective selection and/or control of gaze is an important factor in depressed visual acuity in amblyopic eyes of the first repeat-letter category but not for the third type, in which abnormal lateral interactions may be important. To test the hypothesis that the response to patching and refractive therapy may be less satisfactory in our first category of amblyopic eyes, we are carrying out a prospective study.(ABSTRACT TRUNCATED AT 250 WORDS)

Adolescent↗
PubMed1992

Visual processing of motion-defined form: selective failure in patients with parietotemporal lesions.

The following psychophysical data were obtained from 13 patients with unilateral cerebral hemispheric lesions and 20 control subjects: speed thresholds for detecting and for recognizing motion-defined letters, speed thresholds for detecting coherent motion and for discriminating its direction, and visual acuity for recognizing letters of 96% and 11% contrast. Acuity was between 6/6 and 6/3 for all patients. Four patients showed a selective loss of ability to recognize motion-defined letters, while the ability to detect those same letters was spared, as was the ability to detect coherent motion and discriminate its direction (type I loss). Three patients showed a loss of ability both to recognize and to detect motion-defined letters, while the ability to detect coherent motion and discriminate its direction was spared (type II loss). All seven patients who failed to recognize motion-defined letters had extensive lesions in parietotemporal white matter underlying Brodmann cortical areas 18, 19, 37, 39, 21, and 22. The lesion was in the left hemisphere for three patients and in the right hemisphere for the remaining four. The region of overlap in these seven patients was not invaded by the lesion in any of the other six patients, and none of these six patients showed a loss of ability to recognize motion-defined letters. Three patients showed selective loss of acuity for low-contrast letters with normal Snellen acuity. The lesions in these three patients extended more posteriorly than in any other patient, and their region of overlap was in white matter underlying areas 18 and 19. We conclude that (1) the loss of ability to recognize letters in seven patients was specific to motion-defined letters rather than being a general loss of letter-recognition ability, (2) this visual loss was specific to motion-defined form rather than being a general failure of motion processing, and (3) the visual loss was not produced by lesions that did not involve the localized cerebral region specified above. To explain the existence of type I and of type II loss with sparing of the detection and discrimination of coherent motion, we propose that motion information is processed hierarchically. We further suggest that homologs of the socalled motion and color/form pathways (i.e., areas V1/MT/MST/7a and areas V1/V4/IT) are interconnected to form a distributed system that is important for the recognition of motion-defined form.(ABSTRACT TRUNCATED AT 400 WORDS)

Adult↗
PubMed1992

Defective processing of motion-defined form in the fellow eye of patients with unilateral amblyopia.

The following three measurements were made on a group of 20 pediatric and 5 adult patients with unilateral amblyopia: (1) speed threshold for recognizing motion-defined dotted letters; (2) recognition acuity for isolated solid letters of 4% contrast; and (3) Snellen line acuity for high-contrast letters. Normal limits were established with a group of 30 pediatric and 10 adult control subjects. The main finding was that, in amblyopic children, a high percentage (83%, 15 of 18) of fellow eyes showed a degraded ability to recognize motion-defined letters, even though Snellen acuity and 4% letter acuity were normal for age. The fellow eyes of all nine patients with strabismic amblyopia showed this pattern of loss, as did four of six fellow eyes of patients with anisometropic amblyopia and two of three fellow eyes of patients with anisometropic plus strabismic amblyopia. Only two clinically unaffected eyes were normal for motion-defined letters. These eyes belonged to patients with anisometropic amblyopia. Eighteen of the 19 previously amblyopic eyes tested were abnormal for motion-defined letters even though Snellen acuity was within normal limits for 6 of these eyes. In adults, only one of five fellow eyes failed the motion-defined letter test. It was concluded that the degradation of form perception associated with amblyopia can be different for luminance-defined and motion-defined form and that defective processing of motion-defined form is common in the fellow eyes of children with unilateral amblyopia.

Adolescent↗
PubMed1979

Visually guided locomotion: psychophysical evidence for a neural mechanism sensitive to flow patterns.

Inspecting a radial flow pattern depressed visual sensitivity to changes in the size of a small test square, but only when the square was located near the focus of the flow pattern. The result suggests that precise visual judgments of one's direction of forward motion with respect to the outside world may be mediated by an already known neural organization sensitive to changes in the size of small objects.

Humans↗
PubMed1979

Stereoscopic subsystems for position in depth and for motion in depth.

We describe psychophysical evidence that the human visual system contains information-processing channels for motion in depth in addition to those for position in depth. These motion-in-depth channels include some that are selectively sensitive to the relative velocities of the left and right retinal images. We propose that the visual pathway contains stereoscopic (cyclopean) motion filters that respond to only a narrow range of the directions of motion in depth. Turning to the single-neuron level we report that, in addition to neurons turned to position to depth, cat visual cortex contains neurons that emphasize information about the direction of motion at the expense of positional information. We describe psychophysical evidence for the existence of channels that are sensitive to change size, and are separate from the channels both for motion and for flicker. These changing-size channels respond independently of whether the stimulus is a bright square on a dark ground or a dark square on a bright ground. At the physiological level we report single neurons in cat visual cortex that respond selectively to increasing or to decreasing size independently of the sign of stimulus contrast. Adaptation to a changing-size stimulus produces two separable after-effects: an illusion of changing size, and an illusion of motion in depth. These after-effects have different decay time constants. We propose a psychophysical model in which changing-size filters feed a motion-in-depth stage, and suppose that the motion-in-depth after-effect is due to activity at the motion-in-depth stage, while the changing-size after-effect is due to to activity at the changing-size and more peripheral stages. The motion-in-depth after-effect can be cancelled either by a changing-size test stimulus or by relative motion of the left and right retinal images. Opposition of these two cues can also cancel the impression of motion in depth produced by the adapting stimulus. These findings link the stereoscopic (cyclopean) motion filters and the changing-size filters: both feed the same motion-in-depth stage.

Animals↗
PubMed1979

Selective adaptation to frequency-modulated tones: evidence for an information-processing channel selectively sensitive to frequency changes.

Exposure to an FM tone elevates FM threshold but not AM threshold. This holds for a wide range of frequency deviations (delta F = +/- 0.4 Hz- +/- 30 Hz at least) provided that modulation frequency is low (fm = 2 Hz), but if fm is somewhat higher (e.g., 8 Hz) the finding only holds for small frequency deviations. FM threshold can rise with time up to an adapting duration of at least 1200 s, through this buildup depends on frequency deviation. Exposure to an AM tone elevates AM threshold, but not FM threshold, over a wide range of modulation depths (at least m = 5%--50%). Quasi-FM (QFM) adapting tones resemble FM adapting tones in their effects upon FM and AM sensitivities, even though QFM and AM adapting tones have identical power spectra. Exposure to a pure tone produces no difference between FM and AM threshold elevations. These data can be explained if the human auditory pathway contains separate information-processing channels for AM and FM signals whose sensitivities do not overlap even with suprathreshold stimuli. We suppose that the FM channel (but not the AM channel) is sensitive to changing differences (or ratios) between signals from different sites along the basilar membrane.

Adaptation, Psychological↗