Scotopic sensitivity in coyotes (Canis latrans).

The absolute scotopic limen for light intensity was measured for three 10-mo-old female coyotes. The methodology was similar to that used by Blough in determining psychophysical thresholds in pigeons. Three coyotes were operantly conditioned to depress one of two foot treadles, left or right, depending on the condition of the stimulus light. Scotopic adaptation curves for each coyote were generated. Nonlinear regression curves were then fitted to the raw data. The mean scotopic thresholds did not differ significantly. However, time to the curves' asymptotes did differ significantly for one of the coyotes. The adaptation curves showed a distinct rod-cone "break," and retinal histology confirmed that the coyote has a duplex retina with a preponderance of rods. In addition, electroretinographic analysis showed the relative contributions of rods and cones at various light intensities and indicated a rod-cone break at approximately 15 min. Scotopic spectral sensitivity curves were also generated. The coyotes' scotopic visual threshold is exceeded by the natural illumination available under many nocturnal conditions. The results are discussed in relation to the ecology of the species.     

Brightness perception in the visual field

Summary Apparent brightness was measured at different positions in the visual field for scotopic, mesopic, and photopic adaptation levels by means of a magnitude estimation technique. Apparent brightness of targets with a given luminance remained rather constant throughout the visual field for the mesopic and photopic adaptation level; for the scotopic adaptation level targets in the foveal and perifoveal area had to be more intense in order to appear as bright as targets in the far periphery (beyond 20° eccentricity). For the photopic range, two brightness power functions with different exponents were obtained for the luminance range from 1 to 100 mL at each eccentricity. The exponent for the range from 1 to 10 mL is considerably greater than the exponent beyond 10 mL, and appears to increase with increasing eccentricity.The experiments described in this paper were partly supported by Deutsche Forschungsgemeinschaft and SFB 50-C 6.     

Rod suppression of cone-mediated information about colour and form during dark adaptation

Following substantial bleaches, the specific form and hue thresholds were measured during dark adaptation with a test stimulus of 1 x 2 degrees at 40 degrees extrafoveally. The wavelength of the test field was varied between runs. The results show that both thresholds started to rise at about the cone-rod break of the dark-adaptation curve, irrespective of wavelength used in the test. Furthermore, the specific threshold for form was found to rise when a scotopic stimulus was superimposed on a photopic test flash. On the other hand, both thresholds remained at the cone-plateau level when the test flash was confined within the rod-free fovea. In order to explain the rise in the specific thresholds, it is suggested that signals from rods generated directly in response to the test stimulus may suppress both cone-mediated form and colour. It is also suggested that this type of rod-cone interaction represents a general characteristic involved in several kinds of visual information processing.     

Informational and neural adaptation curves are asynchronous.

Norwich's entropy theory of perception (plus a few additional assumptions) suggests the existence of an "infromational adaptation curves" (change in stimulus equivocation with stimulus duration) for suprathreshold prothetic stimuli that is synchronous with the "neural adaptation curve" (change in firing rate with stimulus duration) observed for sensory neurons. Five experiments are reported in which informational adaptation curves were measured for auditory and visual stimuli by having subjects make absolute identifications of suprathreshold sound or light intenstiies of various durations. Information transmissions for the shortest duration stimuli (1 and 5 msec, respectively, for light and sound) were surprisingly large (small equivocations), indicating that intensity information is acquired very rapidly by the whole organism. The equations of entropy theory were fitted to adaptation data for peripheral sensory neurons (spiral ganglion cells and retinal ganglion cells) and were compared to the informational adaptation curves. It was found that informational adaptation occurred more rapidly than neural adaptation. That is, the two types of adaptation process are asynchronous. However, for both audition and vision, the total amount of information mediated by the adaptation process (channel capacity) was about the same for both types of processes (2.03 bits vs. 2.1 bits per stimulus for sound intensity; 1.3 vs. 2.0 bits per stimulus for light intensity). Faster acquisition could be accomplished in the whole organism through convergent neural circuits that increase sampling rate by pooling the samples taken by individual receptor systems.     

Curve tracing: A possible basic operation in the perception of spatial relations

The two experiments in this study suggest that fast internal tracing of curves is employed by the visual system in the perception of certain shape properties and spatial relations. The experimental task in the first experiment was to determine, as rapidly as possible, whether two Xs lay on the same curve or on different curves in a visual display. Mean response time for “same” responses increased monotonically with increasing distance along the curve between the Xs. The task in the second experiment was to decide either that a curve joining two Xs was unbroken or that the curve had a gap. Decision times again increased as the length of the curve joining the Xs was increased. The results of both experiments suggest that people can trace curves in a visual display internally at high speed (the average rate of tracing was about 40° of visual angle per second). Curve tracing may be an important visual process used to integrate information from different parts of a visual display.     

Behavioral control of visual fixation of the rhesus monkey.

A paradigm for the control of visual fixation of the macaque monkey in vision experiments was described. Using a Maxwellian view, the procedure permits the placement of discrete test-light stimuli in a specific area of the retina as the monkey fixates a primary target. This procedure holds foveal fixation as other behaviorally significant visual stimuli are presented to the visual field. By a methods-of-limits procedure, the sensitivity of the monkey eye was measured at different retinal locations under both photopic and scotopic visual adaptation.     

Light and dark adaptation of visually perceived eye level controlled by visual pitch

The pitch of a visual field systematically influences the elevation at which a monocularly viewing subject sets a target so as to appear at visually perceived eye level (VPEL). The deviation of the setting from true eye level averages approximately 0.6 times the angle of pitch while viewing a fully illuminated complexly structured visual field and is only slightly less with one or two pitched-from-vertical lines in a dark field (Matin & Li, 1994a). The deviation of VPEL from baseline following 20 min of dark adaptation reaches its full value less than 1 min after the onset of illumination of the pitched visual field and decays exponentially in darkness following 5 min of exposure to visual pitch, either 30° topbackward or 20° topforward. The magnitude of the VPEL deviation measured with the dark-adapted right eye following left-eye exposure to pitch was 85% of the deviation that followed pitch exposure of the right eye itself. Time constants for VPEL decay to the dark baseline were the same for same-eye and cross-adaptation conditions and averaged about 4 min. The time constants for decay during dark adaptation were somewhat smaller, and the change during dark adaptation extended over a 16% smaller range following the viewing of the dim two-line pitched-from-vertical stimulus than following the viewing of the complex field. The temporal course of light and dark adaptation of VPEL is virtually identical to the course of light and dark adaptation of the scotopic luminance threshold following exposure to the same luminance. We suggest that, following rod stimulation along particular retinal orientations by portions of the pitched visual field, the storage of the adaptation process resides in the retinogeniculate system and is manifested in the focal system as a change in luminance threshold and in the ambient system as a change in VPEL. The linear model previously developed to account for VPEL, which was based on the interaction of influences from the pitched visual field and extraretinal influences from the body-referenced mechanism, was employed to incorporate the effects of adaptation. Connections between VPEL adaptation and other cases of perceptual adaptation of visual direction are described.     

COLOR THRESHOLD MEASUREMENTS IN SCOTOPIC VISION: Test-stimulation varied

S tabell , U. & S tabell , B. Color threshold measurements in scotopic vision. II. Test-stimulation varied. Scand. J. Psychol ., 1968, 9, 129–132.—The color threshold curve generally coincides with the dark adaptation curve of the rods, irrespectively of test-stimulation variation, confirming the assumption that a threshold response of rods may initiate a color-related process. Variation of color threshold intensity is thus assumed to reflect variation of rod threshold intensity.     

Informational and neural adaptation curves are asynchronous

Norwich’s entropy theory of perception (plus a few additional assumptions) suggests the existence of an “informational adaptation curve” (change in stimulus equivocation with stimulus duration) for suprathreshold prothetic stimuli that is synchronous with the “neural adaptation curve” (change in firing rate with stimulus duration) observed for sensory neurons. Five experiments are reported in which informational adaptation curves were measured for auditory and visual stimuli by having subjects make absolute identifications of suprathreshold sound or light intensities of various durations. Information transmissions for the shortest duration stimuli (1 and 5 msec, respectively, for light and sound) were surprisingly large (small equivocations), indicating that intensity information is acquired very rapidly by the whole organism. The equations of entropy theory were fitted to adaptation data for peripheral sensory neurons (spiral ganglion cells and retinal ganglion cells) and were compared to the informational adaptation curves. It was found that informational adaptation occurred more rapidly than neural adaptation. That is, the two types of adaptation process are asynchronous. However, for both audition and vision, the total amount of information mediated by the adaptation process (channel capacity) was-about the same for both types of processes (2.03 bits vs. 2.1 bits per stimulus for sound intensity; 1.3 vs. 2.0 bits per stimulus for light intensity). Faster acquisition could be accomplished in the whole organism through convergent neural circuits that increase sampling, rate-by pooling the samples taken by individual receptor systems     

RODS AS COLOR RECEPTORS IN PHOTOPIC VISION

Comparing a foveal and an extra-foveal field during dark adaptation, transition from chromatic to achromatic vision at intensity levels above the cone plateau started around the break of the dark adaptation curve. Pre-stimulating the two fields in a dark-adapted state with deep red, and test-stimulating when returning sensitivity had reached absolute threshold of the dark-adapted eye, with green filters at intensities above the specific threshold, the fields matched as to hue and saturation. It appears that rod and cone activities are integrated and function as a synchronized unit during the initial recovery phase of dark adaptation.     

FACILITATION OF CHROMATIC CONE ACTIVITY BY ROD ACTIVITY

STABELL, U. & STABELL, B. Facilitation of chromatic cone activity by rod activity. II. Variation of chromatic-related cone activity. Scand. J. Psychol. , 1971, 12, 168–174.–At the cone-rod break of the dark adaptation curve, the specific threshold was found to drop to lower intensity levels, while the threshold curves of fovea proceeded in one step only, confirming the suggestion that rods may facilitate chromatic-related cone activity.     

COLOR THRESHOLD MEASUREMENTS IN SCOTOPIC VISION: Simultaneous color contrast

S tabell , U. & S tabell , B. Color threshold measurements in scotopic vision. III. Simultaneous color contrast. Scand J. Psychol ., 1968, 9, 133–137.—Color may be observed well below the break-point level of the dark adaptation curve, suggesting that the impulse pattern initiated in the rods may trigger a color-related response. Color is induced when the intensity of the inducing field reaches a certain level above the specific threshold, provided the stimulation of the test field is observable.     

Effects of absolute luminance and luminance contrast on visual search in low mesopic environments

Diverse adaptive visual processing mechanisms allow us to complete visual search tasks in a wide visual photopic range (>0.6 cd/m²). Whether search strategies or mechanisms known from this range extend below, in the mesopic and scotopic luminance spectra (<0.6 cd/m²), has yet to be addressed. Based on a study that addressed simple target discrimination in luminance environments using contrast-dependent behavioral efficiency functions, we assessed visual search in more complex-feature and conjunction-search paradigms. The results verify the previously reported deficiency windows defined by an interaction of base luminance and luminance contrast for more complex visual-search tasks. Based on significant regression analyses, a more precise definition of the magnitude of contribution of different contrast parameters. Characterized feature search patterns had approximately a 2.5:1 ratio of contribution from the Michelson contrast property relative to Weber contrast, whereas the ratio was approximately 1:1 in a serial-search condition. The results implicate near-complete magnocellular isolation in a visual-search paradigm that has yet to be demonstrated. Our analyses provide a new method of characterizing visual search and the first insight in its underlying mechanisms in luminance environments in the low mesopic and scotopic spectra.

     

Mental curve tracing with elementary stimuli

It has been proposed that certain spatial relations are determined by an operation, or "visual routine," that can trace along a boundary (Ullman, 1984). This proposal was supported by Jolicoeur, Ullman, and Mackay's (1986) finding that the time required to determine if two Xs are on the same curve increased monotonically with the separation of the Xs along that curve. In the present study the generality of the curve tracing hypothesis was explored across four experiments by using elementary stimuli that eliminated interweaving curves, displaced the fixation point away from the curves and target Xs, and provided a simple alternative to curve tracing--namely, determining whether or not the Xs fell on the same side of the figure. Stimuli consisted of two curves (150 degrees arcs) and two Xs, and each stimulus was presented for 150 ms. In Experiments 1 and 2, subjects were instructed to decide as quickly as possible if the two Xs fell on the same curve or on different curves. Even for these elementary stimuli, mean reaction time (RT) for same trials increased monotonically with the distance separating the Xs. Mean RT for different trials, however, decreased with the distance separating the Xs. In Experiments 3 and 4 alternatives to curve tracing were tested. For same trials the evidence strongly favored curve tracing. However, different trials were apparently solved on the basis of judgmental processes presumably operating in parallel with curve tracing. Curve tracing rates fluctuated across experiments and seemed to be partially governed by the width of the "pathway" provided for the trace.     

Auditory Acuity and Musical Ability in the First Four Grades

The height of the b-wave in the electroretinogram of the turtle Pseudemys was used as an index of spectral sensitivity under conditions of light and dark adaptation. A series of discontinuous wavelengths of equal energy was used as stimuli. The peak scotopic sensitivity occurred in the region of 559 μ while the maximal sensitivity under photopic conditions occurred at approximately 658 μ. Although the present methods do not allow a precise localization of the peaks of these two visual functions, the values are accurate within approximately 15 μ either side of the stated peaks.     

Letter recognition at low contrast levels: effects of letter size

Contrast variation was used to measure recognition thresholds for lowercase letters, with the aim of obtaining a better understanding of the role that early stages of visual processing play in letter recognition. Frequency-of-recognition curves were measured for alphabets of different letter size. Since variation of the adaptational state of the eye changes the characteristics of primary visual processing in a quantifiable way, recognition thresholds were measured both at a high (150 cd m-2) and at a low (0.9 cd m-2) adaptation level. Thresholds decreased as letter size increased, in a way comparable with data on visual acuity. At the lower adaptation level, recognition thresholds became higher, which is also in accordance with visual acuity data. Furthermore, the slopes of the frequency-of-recognition curves for alphabets as a function of log contrast decreased with decreasing letter size. It is argued that this is mainly caused by an increasing dispersion of internal representations of individual letters on the internal psychological scale as letter size decreases.     

Spare the rod and spoil the icon

Short-term visual storage was investigated with a successive field paradigm, so that correct performance depended upon combining visual information from two targets that were never on simultaneously. In the first two experiments, the stimuli consisted of two slides, each containing a 10' red dot on a gray surround, and separated by an interstimulus interval (ISI) from 20 to 400 msec. Subjects had to determine if the dots were vertically or horizontally aligned. In Experiment 1, the stimuli had either no contrast for the rods or no luminance contrast for the cones or high contrast. At short ISIs the cone contrast determined performance, whereas at long ISIs the rod contrast determined performance. In fact, when the dots were invisible to the rods, the task was impossible for long ISIs. In Experiment 2, performance was compared for zero log rod contrast and for small departures from zero. Even a small departure from zero log rod contrast resulted in above-chance performance. In Experiment 3, the stimuli were luminous rectangles and the task was to decide whether or not a 4' spatial gap was present between the two successively presented rectangles. Wavelength, luminance, and ISI were varied under both photopic and scotopic adapting conditions. The result was that the rods performed the task for ISIs of 150 msec or longer under scotopic conditions and under the photopic conditions that we were able to test. The results of the experiments taken together are consistent with the hypothesis that the cone icon is short, whereas the rod icon is robust and long lasting.     

Behavioural adaptation or constraint? The effect of curve proximity on driving behaviour

Horizontal curves are typically associated with increased crash risk when compared with straight roads, but recent analyses have suggested that having more frequent sharp curves decreases the relative crash risk posed by each curve. Here, 90 drivers completed a simulated rural drive with either high proximity (160 m straight tangent between curves) or low proximity (1200 m tangent) curves. Curve proximity had a significant effect on approach speeds, with drivers in the high proximity curve drive showing significantly lower mean and maximum approach speeds before entering the curve. However, they also showed an unexpected tendency to higher speeds while negotiating the curve itself. The current study provides direct empirical evidence that driving behaviour on approach to a given curve is significantly affected by the proximity of other curves, and therefore highlights the need to factor in the characteristics of the road on approach to the curve, as well as the features of the curve itself when assessing risk.     

Long-term potential for imprinting in ducks and chickens

In the first of five experiments, three of four adult ducks who had been reared in visual isolation gradually developed strong approach responses towards a moving panel of colored lights. Experiment 2 provided evidence that the ducks' approach response reflected the same sort of social attachment that is typically formed to moving objects by newly hatched ducklings. Experiment 3 revealed that the fourth duck would not approach the moving stimulus even after additional exposure to it, but would approach a conspecific after group housing had been enforced for seven days. In Experiment 4, none of five adult chickens who had been reared in visual isolation developed approach responses towards the moving stimulus, even though in Experiment 5, newly hatched chicks approached the stimulus quite readily. Taken together, these findings (a) indicate that ducks retain the ability to form filial-type attachments to novel objects throughout their lives, and (b) offer preliminary evidence that chickens do not retain this ability into adulthood.     

Scotopic and photopic afterimages

Stabell, U. & Stabell, B. Scotopic and photopic afterimages. Scand. J. Psychol., 1973, 14, 210–212.MdashThe curves of photopic and scotopic afterimages were found to coincide, confirming the suggestion that disposition for scotopic contrast hue is controlled basically by the ratio of hue-related processes initiated upon chromatic prestimulation of cones, while the achromatic test-stimulation is a constant stimulus, regardless of test variables.